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_LN831790	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) chromosome 1	16 crisprs	DEDDh,DinG,csa3,WYL,c2c9_V-U4,cas3,Cas9_archaeal,cas4,cas5,cas8c,cas7,cas1,cas2	7	17	2	0
NZ_LN831789	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE2	0 crisprs	RT	0	0	0	0
NZ_LN831788	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence	0 crisprs	WYL,DEDDh	0	0	1	0

1. NZ_LN831790

CRISPR-Cas detection and classification

Crispr_ID: NZ_LN831790_1

• CRISPR_ID: NZ_LN831790_1
• CRISPR_location: 2331985-2332178
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_1

Consensus_repeat	Method
TGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAACCACG	CRISPRCasFinder

spacers of NZ_LN831790_1

>1.1|2332033|98|NZ_LN831790|CRISPRCasFinder
GTACGGCGAGCGCCCGGGGCCAGCATGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAGCCACGGTACGGCGAGCACCCGGGGCCAGCG

CRISPR arrays and Neighbor proteins around NZ_LN831790_1

CRISPR arrays

The CRISPR arrays of NZ_LN831790_1

>merge|NZ_LN831790|1|2331985-2332178|CRISPRCasFinder
CGGTGCGGCGGTGCCTGGGGCGCGGCGGGGGCCCGGGGCACAGCCACGGTACGGCGAGCGCCCGGGGCCAGCATGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAGCCACGGTACGGCGAGCACCCGGGGCCAGCGTGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAACCACG

>NZ_LN831790|1|1|2331985-2332178|CRISPRCasFinder
CGGTGCGGCGGTGCCTGGGGCGCGGCGGGGGCCCGGGGCACAGCCACG	GTACGGCGAGCGCCCGGGGCCAGCATGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAGCCACGGTACGGCGAGCACCCGGGGCCAGCG
TGACGCGACGGTGCCTGGAGCGTGGCGGGGGCCCAAGGCGCAACCACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029382752.1|2322327_2322735_-|hypothetical-protein	unknown	unknown	gnl|CDD|212151
NZ_LN831790.1|WP_029382750.1|2323904_2325311_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831790.1|WP_029382749.1|2325320_2326007_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831790.1|WP_029382745.1|2328839_2329733_+|amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|223836
NZ_LN831790.1|WP_047121692.1|2333196_2333628_+|sulfurtransferase	unknown	unknown	gnl|CDD|236337
NZ_LN831790.1|WP_029382753.1|2321598_2322012_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029382748.1|2326299_2327076_+|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224051
NZ_LN831790.1|WP_029382740.1|2334659_2335784_-|recombinase-RecA	unknown	unknown	gnl|CDD|236476
NZ_LN831790.1|WP_029382751.1|2322842_2323838_+|TAXI-family-TRAP-transporter-solute-binding-subunit	unknown	unknown	gnl|CDD|270287
NZ_LN831790.1|WP_029382738.1|2337390_2337585_-|DUF3046-domain-containing-protein	unknown	unknown	gnl|CDD|378612
NZ_LN831790.1|WP_047121693.1|2336100_2337261_-|AI-2E-family-transporter	unknown	unknown	gnl|CDD|279875
NZ_LN831790.1|WP_029382746.1|2328177_2328843_+|amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|223836
NZ_LN831790.1|WP_029382741.1|2333747_2334656_-|recombination-regulator-RecX	unknown	unknown	gnl|CDD|234646
NZ_LN831790.1|WP_029382744.1|2329908_2331573_+|FAD-dependent-monooxygenase	unknown	unknown	gnl|CDD|236158
NZ_LN831790.1|WP_029382736.1|2338785_2343717_+|ATP-dependent-helicase	unknown	unknown	gnl|CDD|137505
NZ_LN831790.1|WP_029382743.1|2332672_2333200_+|cysteine-dioxygenase	unknown	unknown	gnl|CDD|283616
NZ_LN831790.1|WP_029382735.1|2343876_2344698_+|Fpg/Nei-family-DNA-glycosylase	unknown	unknown	gnl|CDD|223344
NZ_LN831790.1|WP_029382737.1|2337667_2338603_+|hypothetical-protein	unknown	unknown	gnl|CDD|239219
NZ_LN831790.1|WP_029382734.1|2344704_2345190_-|SRPBCC-domain-containing-protein	unknown	unknown	gnl|CDD|176856
NZ_LN831790.1|WP_029382747.1|2327256_2328093_+|glutamate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270408

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029382752.1|2322327_2322735_-|hypothetical-protein	gnl|CDD|212151	cd11544, NTP-PPase_DR2231, Nucleoside Triphosphate Pyrophosphohydrolase (EC 3.6.1.8) MazG-like domain found in Deinococcus radiodurans DR2231 protein and its bacterial homologs. This family corresponds to the DR2231 protein, a MazG-like NTP-PPase from Deinococcus radiodurans, and its bacterial homologs. All family members contain a well-conserved divalent ion binding motif, EXXEX(12-28)EXXD, which is the identity signature for all-alpha-helical NTP-PPase superfamily. DR2231 shows significant structural resemblance to MazG proteins, but is functionally related to the dimeric dUTPases. It might be an evolutionary precursor of dimeric dUTPases with very high specificity in hydrolyzing dUTP into dUMP, but an inability to hydrolyze dTTP, a typical feature of dUTPases. Moreover, unlike the dUPase monomer containing a single active site, the DR2231 protein dimer holds two putative active sites.	2.11569e-50
NZ_LN831790.1|WP_029382750.1|2323904_2325311_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	5.25377e-51
NZ_LN831790.1|WP_029382749.1|2325320_2326007_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	2.57817e-78
NZ_LN831790.1|WP_029382745.1|2328839_2329733_+|amino-acid-ABC-transporter-permease	gnl|CDD|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	1.2492e-51
NZ_LN831790.1|WP_029382744.1|2329908_2331573_+|FAD-dependent-monooxygenase	gnl|CDD|236158	PRK08132, PRK08132, FAD-dependent oxidoreductase; Provisional.	3.06743e-57
NZ_LN831790.1|WP_029382743.1|2332672_2333200_+|cysteine-dioxygenase	gnl|CDD|283616	pfam05995, CDO_I, Cysteine dioxygenase type I. Cysteine dioxygenase type I (EC:1.13.11.20) converts cysteine to cysteinesulphinic acid and is the rate-limiting step in sulphate production.	1.44321e-49
NZ_LN831790.1|WP_029382748.1|2326299_2327076_+|amino-acid-ABC-transporter-ATP-binding-protein	gnl|CDD|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	3.65026e-154
NZ_LN831790.1|WP_029382740.1|2334659_2335784_-|recombinase-RecA	gnl|CDD|236476	PRK09354, recA, recombinase A; Provisional.	0
NZ_LN831790.1|WP_029382751.1|2322842_2323838_+|TAXI-family-TRAP-transporter-solute-binding-subunit	gnl|CDD|270287	cd13569, PBP2_TAXI_TRAP_like_1, Substrate binding domain of putative TAXI proteins of the tripartite ATP-independent periplasmic transporters; the type 2 periplasmic binding protein fold. This subgroup includes uncharacterized periplasmic binding proteins that are related to Thermus thermophilus GluBP (TtGluBP) of TAXI-TRAP family. TRAP transporters are comprised of an SBP (substrate-binding protein) and two unequally sized integral membrane components. Although TtGluBP is predicted to be an L-glutamate and/or an L-glutamine-binding protein, the substrate spectrum of TAXI proteins remains to be defined. A sequence-homology search also shows that TtGluBP shares low sequence homology with putative immunogenic proteins of uncharacterized function.	5.76012e-101
NZ_LN831790.1|WP_029382738.1|2337390_2337585_-|DUF3046-domain-containing-protein	gnl|CDD|378612	pfam11248, DUF3046, Protein of unknown function (DUF3046). This family of proteins with unknown function appears to be restricted to Actinobacteria.	7.90653e-33
NZ_LN831790.1|WP_047121693.1|2336100_2337261_-|AI-2E-family-transporter	gnl|CDD|279875	pfam01594, AI-2E_transport, AI-2E family transporter. This family includes four different proteins from E. coli alone. One of them, YdgG or TqsA, has been shown to mediate transport of the quorum-sensing signal autoinducer 2 (AI-2). It is not clear if TqsA enhances secretion of AI-2 or inhibits AI-2 uptake. By altering the intracellular concentration of AI-2, TqsA affects gene expression in biofilms and biofilm formation. TsqA belongs to the AI-2 exporter (AI-2E) superfamily.	1.73479e-73
NZ_LN831790.1|WP_029382746.1|2328177_2328843_+|amino-acid-ABC-transporter-permease	gnl|CDD|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	1.25173e-47
NZ_LN831790.1|WP_029382741.1|2333747_2334656_-|recombination-regulator-RecX	gnl|CDD|234646	PRK00117, recX, recombination regulator RecX; Reviewed.	1.39949e-41
NZ_LN831790.1|WP_047121692.1|2333196_2333628_+|sulfurtransferase	gnl|CDD|236337	PRK08762, PRK08762, molybdopterin-synthase adenylyltransferase MoeB.	7.48142e-18
NZ_LN831790.1|WP_029382736.1|2338785_2343717_+|ATP-dependent-helicase	gnl|CDD|137505	PRK09751, PRK09751, putative ATP-dependent helicase Lhr; Provisional.	0
NZ_LN831790.1|WP_029382737.1|2337667_2338603_+|hypothetical-protein	gnl|CDD|239219	cd02889, SQCY, Squalene cyclase (SQCY) domain; found in class II terpene cyclases that have an alpha 6 - alpha 6 barrel fold. Squalene cyclase (SQCY) and 2,3-oxidosqualene cyclase (OSQCY) are integral membrane proteins that catalyze a cationic cyclization cascade converting linear triterpenes to fused ring compounds. Bacterial SQCY catalyzes the convertion of squalene to hopene or diplopterol. Eukaryotic OSQCY transforms the 2,3-epoxide of squalene to compounds such as, lanosterol (a metabolic precursor of cholesterol and steroid hormones) in mammals and fungi or, cycloartenol in plants. Deletion of a single glycine residue of Alicyclobacillus acidocaldarius SQCY alters its substrate specificity into that of eukaryotic OSQCY. Both enzymes have a second minor domain, which forms an alpha-alpha barrel that is inserted into the major domain. This group also contains SQCY-like archael sequences and some bacterial SQCY's which lack this minor domain.	0.00673215
NZ_LN831790.1|WP_029382735.1|2343876_2344698_+|Fpg/Nei-family-DNA-glycosylase	gnl|CDD|223344	COG0266, Nei, Formamidopyrimidine-DNA glycosylase [DNA replication, recombination, and repair].	5.37461e-61
NZ_LN831790.1|WP_029382734.1|2344704_2345190_-|SRPBCC-domain-containing-protein	gnl|CDD|176856	cd07814, SRPBCC_CalC_Aha1-like, Putative hydrophobic ligand-binding SRPBCC domain of Micromonospora echinospora CalC, human Aha1, and related proteins. This family includes the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of Micromonospora echinospora CalC, human Aha1, and related proteins. Proteins in this group belong to the SRPBCC domain superfamily of proteins, which bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket. MeCalC confers resistance to the enediyne, calicheamicin gamma 1 (CLM), by a self sacrificing mechanism which results in inactivation of both CalC and the highly reactive diradical enediyne species. MeCalC can also inactivate two other enediynes, shishijimicin and namenamicin. A crucial Gly of the MeCalC CLM resistance mechanism is not conserved in this subgroup. This family also includes the C-terminal, Bet v1-like domain of Aha1, one of several co-chaperones, which regulate the dimeric chaperone Hsp90. Aha1 promotes dimerization of the N-terminal domains of Hsp90, and stimulates its low intrinsic ATPase activity, and may regulate the dwell time of Hsp90 with client proteins. Aha1 can act as either a positive or negative regulator of chaperone-dependent activation, depending on the client protein, but the mechanisms by which these opposing functions are achieved are unclear. Aha1 is upregulated in a number of tumor lines co-incident with the activation of several signaling kinases.	1.58972e-30
NZ_LN831790.1|WP_029382747.1|2327256_2328093_+|glutamate-ABC-transporter-substrate-binding-protein	gnl|CDD|270408	cd13690, PBP2_GluB, Substrate binding domain of ABC glutamate transporter; the type 2 periplasmic binding protein fold. This group includes periplasmic glutamate-binding domain GluB from Corynebacterium efficiens and its related proteins. The GluB domain belongs to the type 2 periplasmic binding protein fold superfamily (PBP2), whose many members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. 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 receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.89465e-91

Protein sequences

>NZ_LN831790.1|WP_029382744.1|2329908_2331573_+|FAD-dependent-monooxygenase
MDPVIIAGAGPVGLTLALALARQEVPCVVLDEGPGKDEPRPARTVVLHEDTADLLERLTGLPLTRTGVRWAGWRSMRRKQVTREIRFDGGAEDEHRDGPEEQDGDTAPAPLHLPQHVLTGALRTALARETLVKVAVDSRLDTIEQESSGVTAHARGPKGAWWRGSYLVGCDGPRSTVRKLQDIRFPGRTAVERHAVAALRTQLPWPGEALLHRTPPWRMSGPSAGEITARPLPDGVWRLDWLLPPGKDLVTPELLVTRIRETLTGWTGDSAPAYELLDTGVHIVHHRLARRWRVGRVFLAGDAAHLLGALGTQGLDEGLRDAGNLAWKLALAWHHGPHEALLDSYQAERRAAIAARLRATDQVLPLLRGGGGLRACLPGSARGHDALLADGHLGRGALGAPAVYSGSPLAPPRLDGEVPVGTPPGAPVTDVRVTAEDGTFVRLRDRLGRGALLVVLIAPGTGVWERKHWVTAGVMPRLAAAVTALPCRAELLVAESYPGAAAHTVLLVRPDGHLVTALGGVRPADLYTAAEAAVGGGAARTTAGAGAAAAGPGA
>NZ_LN831790.1|WP_029382745.1|2328839_2329733_+|amino-acid-ABC-transporter-permease
MSSVLYDAQGPRAKRRNVLFTVVFLVALAALLWWVYRALDEKGQLEWAKWEMFFTGTEAWSTYIWPGLKNTLTAAVLSVLIALPLGAVLGISRLSDHVWIRVPAALVVEFFRAIPVLVLMIFGLALFAQYTDVSTDDRPLYAVITGLVLYNASVLAEIVRAGILALPKGQSEAAMAIGLRKGQVMRVILLPQAVTAMLPAIVSQLVVIVKDTALGGAILTFPEMLSAASTMSAYYGANTIASFTVVAVIFIAINFALTSFASWLERRLRRAKKSTGAVLAADDNQPNAGATAGGGTF
>NZ_LN831790.1|WP_029382746.1|2328177_2328843_+|amino-acid-ABC-transporter-permease
MFDFLEGYDLLGAFWTTVQLTVLSAVGSLIWGTLLAAMRVGPVPLMRGFGTAYVNIVRNIPLTVIILFTSLGLNQTLSVQLGSDDFDTINFRLAVLGLILYTSAFVCEALRSGINTVPVGQAEAARAIGLSFSQVLGLVVLPQAFRSSVVPLANVLIALTKNTTVAAAIGVAEAALLMKEMIENEAALLLIAAIFAFGFVCLTLPTGLILGWVGKKVAVKR
>NZ_LN831790.1|WP_029382747.1|2327256_2328093_+|glutamate-ABC-transporter-substrate-binding-protein
MKLRKVSAASATVLALALTATACGGDGGDDNGSSGGGKKITIGIKFDQPGLGQKTPQGYAGFDVDVATYVAKKLGYEEDQIEWRESKSADRETMLQRGDVDFIVATYSITPQRQEKVDFAGPYLLAHQDVLIRADDDSIKSPEDLNNKKLCSVTGSTSAQNVKEKLAPKAQLQNYTTYSACLGGLQNGAIDALTTDDSILAGYAAQSQFKGKFKLGGFKMTNENYGIGVKKGSDLKDKINKALEDMVADKSWDKAVQDNFGPANYKNEPAPKIGDIKS
>NZ_LN831790.1|WP_029382748.1|2326299_2327076_+|amino-acid-ABC-transporter-ATP-binding-protein
MTEVSVAKNDVAATDELVVLKSVNKHFGALHVLQDIDLTIARGEVVVVIGPSGSGKSTLCRTINRLETIDSGTISIDGKPLPQEGKALARLRADVGMVFQSFNLFAHKTVLENVTLGQIKVRKADRKQAEEKARGLLDRVGVAAQADKYPAQLSGGQQQRVAIARALAMDPKVMLFDEPTSALDPEMINEVLEVMQQLARDGMTMIVVTHEMGFARSAANRVVFMADGRIVEEAAPDQFFSNPRSDRAKDFLSKILHH
>NZ_LN831790.1|WP_029382749.1|2325320_2326007_-|response-regulator-transcription-factor
MRLLLVEDDNHVAAALSAVLARHGFEVTHARSGEEALQALVPGGSGFGVVLLDLGLPDQDGYEVCGKIRKRTSTPVIMVTARADVRSRIHGLNLGADDYVVKPYDTGELLARIHAVSRRTAHEEAAPGGEGALRLGPVQIELPTRRVSVDGTAVQLTRKEFDLLALLAQRPGVVFRREQIISEVWRTSWEGTGRTLEVHVASLRAKLRLPALIETVRGVGYRLVAPGS
>NZ_LN831790.1|WP_029382750.1|2323904_2325311_-|HAMP-domain-containing-histidine-kinase
MRARLLPLLIVLMAAVLLALGIPLAISVAAAQQQQVVVDRIDDTARFAALAQFVTDAPYGSRPVSTDERLETLQRELTSYHEVYDIRAGVFYRNHIPMANAPTTWFLPQTGEVRSAFDEALLSRRSHDPEQVWPWERGRLVVASPVIRDGDVVAVVVTDSPTGPMRSRTLHGWLVIGAGEAAAMLLAVGAALRLTGWVLRPVRVLDATTHDIATGRLKSRVAPAGGPPELRRLAKSFNEMADNLEDVLVQQRAFVADASHQLRNPLAALLLRIELLALELPEGNQEIASVQAEGKRLARVLDDLLDLALAEHAEPDLGLTDIGALAAERVAAWAPTAEAKGVRLVGECPATTGWADPVALSSALDAVVDNAVKFTPPEGTVRVTVASNGATATVVVTDTGPGLTDEELTRVGDRFWRSGRHQNVKGSGLGLSICRALLEAGGGSVTFGHHAPRGLKVTVTVPRTAPAA
>NZ_LN831790.1|WP_029382751.1|2322842_2323838_+|TAXI-family-TRAP-transporter-solute-binding-subunit
MSTLFRRIGRRRALQGAAAGVVALGLLLWWLLPLGEEPPRGSIAFSTGTRAGVYQKYGELLRTELHRDMPDLRVRLLTSAGSQENVERVATGKADFTIAAADAVETYKLSGRPGADRLRGVARLYDDYVQLVVPVDSGIRSVADLRGKRVAIGLPHSGVRLIATRLLLAAGIDPEKDITARSDGIDTGPRRLGEAVDAFFWSGGLPTDGLRQIAEEAAFRFIPVGEDLVARLHEDGGATRYYRATSIPESAYPTVQNGSSVPTMAVSNLLITREDTDPRLAEWLTRTVIESRDGIGAHVHSAQLVDLRTAIYTDPLPLHEGARRYYRSVKP
>NZ_LN831790.1|WP_029382752.1|2322327_2322735_-|hypothetical-protein
MSSSSPADLVRAFHLAFGLDARSTPGEVPPELAAQRGRLLAEEAAEVAEVSVRGPLDRLAHELADVVYVAYGTALVHGIDLDAVIAEIHRSNMTKLGPDGQVARRADGKVLKGEHYRAPDVAGVLRRQGWAPDGA
>NZ_LN831790.1|WP_029382753.1|2321598_2322012_+|hypothetical-protein
MEITKSSTILFRNTMRITNGHLDGFRRAIAQAVAFAQEHGPQLMVEVFIDEERMLAHSFQLYRDSDAIRAHWRLSDPYIREVMEHCTVQHFEIFGAPDHDIVAALKTPDGESFPFVVSPRLAGFNRLGTPGSGESHS
>NZ_LN831790.1|WP_029382743.1|2332672_2333200_+|cysteine-dioxygenase
MSAPASSAPAVAPPTEAGLLDFARRAAADPALIASLPLDPHGRTWVRLEGPGGSEAWLIGWPPGSGTGWHDHADSVGAFVTASGELTEHSLAARLPTEGWTSLELTAGVDRDRRLAAGQGRAFGRHHVHEVLNESPVRHAISVHAYYPPLPRIRRYSRTGQVLRLEQVERPEDWQ
>NZ_LN831790.1|WP_047121692.1|2333196_2333628_+|sulfurtransferase
MSGGTPDRPVAGASGRPLGIDALLERVRRGYERIGPREAYEAAAAGEALLVDIRYAALHERDGLIPGALVVERNELEWRLDPLGSHRLPEATGHGLRIVVVCNEGYASSLAAESLHRLGLRRATDLVGGFQAWRAAGLPVTPP
>NZ_LN831790.1|WP_029382741.1|2333747_2334656_-|recombination-regulator-RecX
MTRRTDWAEYACPDAAAREREQGRADGSSAGAAGDGYGGYSGYGGYRAAPGGRGYGAEEAPFRADAATHGGYGDGADGGAADGDGSPGEGGTRRSGGRTRGASGGSRGRGRRGRGEPFAEDGGTSSSSRAEKGEPPGDPVEQARAICLRLLTGTPRTRKQLADALRKRQIPDDAAEEVLSRFEEVGLIDDGAFADAWVESRHHGRGLARRALARELRTKGVDPALVDAAVSQLDSEQEEATARELVARKLRSTRGLDRDRRLRRLAGMLARKGYPEGMALKVVRQALEEEGEDTDFLDEGAF
>NZ_LN831790.1|WP_029382740.1|2334659_2335784_-|recombinase-RecA
MAGTDREKALDAALAQIERQFGKGAVMRMGERSKEPIEVIPTGSTALDVALGVGGLPRGRVVEIYGPESSGKTTLTLHAVANAQKAGGQVAFVDAEHALDPEYARKLGVDIDNLILSQPDNGEQALEIVDMLVRSGALDLIVIDSVAALVPRAEIEGEMGDSHVGLQARLMSQALRKITSALNQSKTTAIFINQLREKIGVMFGSPETTTGGRALKFYASVRIDIRRIETLKDGTEAVGNRTRCKVVKNKVAPPFKQAEFDILYGQGISREGGLIDMGVEHGFVRKAGAWYTYEGDQLGQGKENARNFLKDNPDLANEIERKIKEKLGVGVRPEEPAAEPGKDAAVPAAAADAATVPAPATAKVTKSKAAAAKS
>NZ_LN831790.1|WP_047121693.1|2336100_2337261_-|AI-2E-family-transporter
MPRWLPRAMVLALALYAVFQLGSWAFHQLIGLLINVLIAFFLALAVEPAVSWMAARGMRRGLATGLVFLAVMIVAAGFVTLLGSMLAGQIIKMVEGFPDYLDSVINWVNTHFHTDLRRVDIQEGVLRSDWLRNYVQNSATGVLDVSAQVLGGLFQLLTITLFSFYFAADGPRLRRALCSVLPPARQAEVLRAWEIAVNKTGGYLYSRGLMALISGIAHYILLEVLGVPYAPVLAVWVGLVSQFIPTIGTYLAGALPMLIAFTVDPWYALWVLIFVVVYQQFENYVLQPKLTSKTVDIHPAVAFGSVVAGTALLGAVGALIAIPAVATLQAFLGAYVKRYDVTDDPRVHGHRGPRTGPGLLTRARRLWDGRAGAGGPKKPGPGEGPS
>NZ_LN831790.1|WP_029382738.1|2337390_2337585_-|DUF3046-domain-containing-protein
MRLTVFWQRMADHFGPGYADTFARDHVMTELGGRTVRQALDAGWDAKDVWRVVCTVMNVPQDKR
>NZ_LN831790.1|WP_029382737.1|2337667_2338603_+|hypothetical-protein
MAETGASALPPARSPLARAERFVWLTARVLEQRLFAHHFRDGGAGPVETALDAYRNEDGGYGHALEPDLRGPVSQPLHTARALRVLDALGRCGGPRVERVCRYLTAVSTPDGALPAVHPSQRGYPAAPFVPVVDDPPSDLLATGPVVGLLHRNEVWHAWLFRATDFCWQRIESLRTTHPYEVEAAVAFLDCAPDRPRAEAAADRLGRLVREQRLAVLEPDRLDRYPVSPGYAPGEHHFPHDYAPAPGSLARAWFTDDEMARSLDFLAAAQQEDGGWPIRWRRWAPAPALEARPLVTLDALLTLTAYGRPVD
>NZ_LN831790.1|WP_029382736.1|2338785_2343717_+|ATP-dependent-helicase
MVSSAHRALDGFSPATRGWFSGAFSAPTAAQAGAWQAIREGSDVLVVAPTGSGKTLAAFLAALDQLASTPPPADPKKRCRVLYVSPLKALAVDVERNLRSPLTGIRHEAVRLGLPEPEVKVGIRSGDTPAAERRALSTRPPDILITTPESLFLMLTSAAREALTGVETVILDEVHAVAGTKRGAHLALSLERLDELLPRPARRIGLSATVRPVDEVARFLSPRRKVEVVQPESGKEFDLSVVVPVEDLGELGGSPAADNGEGAERPSIWPHVEERITDLVQSHRSTIVFANSRRLAERLCNRLNEIAYERATGEPLGEHHAPAELMGNSGSAQGAPAIIARAHHGSVSKEQRALVEEDLKAGRLPAVVATSSLELGIDMGAVDLVVQVESPPSVASGLQRVGRAGHQVGAVSTGVVFPKYRGDLVQAAVVTERMRSGAIESLRIPANPLDVLAQQLVAMTALDTWQVDDLLATVRRAAPFASLPESAFTAVLDMLAGRYPSDAFAELRPRVVWDRVAGTVTGRPGAQRLAVTSGGTIPDRGLFGVFLAGADPKKGGGRVGELDEEMVYESRVGDVFTLGTSSWRIEDITRDRVLVSPAPGVPGRLPFWKGDQLGRPLELGRALGAFLREVGSLPKEDARLRLLTAGLDAWAADNVLSYLDEQREACGHVPDDRTIVVERFRDELGDWRVVVHSPFGAQVHAPWALALGARLSERYGMDAQVMHADDGIVLRLPDADLMGLDLLDQEPARAGTEYDADRAPVGAADVVFDKGEVDRIVTDQVGGSALFAARFRECAARALLLPRRNPGKRTPLWQQRQRAAQLLEVASEYGSFPIVLEAVRECLQDVFDVPGLVELMGDLESRKVRLVEVTTPEPSPFARSLLFGYVAQFLYEGDSPLAERRAAALSLDSRLLAELLGQAELRELLDAEVLTELERELQWLTEDRRVKDVEGVADVLRVLGPLTDAELAERGAEPGWAEELAAARRAIRVRIARADHWAAVEDAGRLRDALGTALPVGVPEAFTEPVKDPLGDLLARYARTHGPFTSVTAAARFGLGVAVTEGALQRLAATGRIVQGEFHPAGIGQEWCDATVLRRLRRRSLAALRHELEPVPPAALAQFLPQWQHIGKGHALRGIDGLVRALEQLQGAAVPASALEKLVLPSRVAHYTPAMLDELTAAGEVVWAGAGSLPGKDGWVSLYLADAAPLLLPPPHPLELTALHQSVLDTLSGGYGLFFRQIADQVRATTHPDVTDPQLADALWDLAWSGRLTNDTLAPLRSLLGSGRTAGSTAHRARRTVPRGRYGSLTAAARTASRSGPPTVAGRWSLLPAREADTTVRAHALARTLLDRHGVVTRGAVAAEGVEGGFSATYRVLSVFEESGQARRGYVVEGLGAAQFAMDGAVDRLRAVANARERDEALPGPGFPDGGPQDATADGTPDWLAPGTDYTPDWLTPELPGAPGSPDRLAPGDYISPHDYDAPGAGGPRGGAARNAPGAPWSTHRRPGQGPGGRSSPASRAVVLAAADPANAYGAALAWPEPPAGASHKPGRKAGSLVVLVDGELTLYMERGGKTLLAWPSSPDGEEAHDPRLHAAVEALAAAAREGALGTVTVERVNGAAALTSPFGALLETAGFVATPRGLRLRA
>NZ_LN831790.1|WP_029382735.1|2343876_2344698_+|Fpg/Nei-family-DNA-glycosylase
MPEGDTVWQTARRLHGALAGEVLIRSDFRVPRYATVDLTGRRVLDVVSRGKHLLTRIEGGLTLHSHLRMDGSWKVFAAGRRWSGGPAHQIRVVLGSADRTAVGYRLPVLELLRTADEHRVVGHLGPDLLGPDWDPAQALANLLADPARPLGEALLDQRNLAGIGNVYKCELCFLLGVTPWLPVGDLPAERAGKLPVLAKKLLEANRDRPVRGTTGRRGQDLFVYGRAPRPCLRCNTSVRVADQGDGSRERPTYWCPTCQRGPTPAPRGRTGAR
>NZ_LN831790.1|WP_029382734.1|2344704_2345190_-|SRPBCC-domain-containing-protein
MSVTSVDRDVDHLALTLVADFAAPVERVWQMWADPRRLERWWGPPDYPATVEEHDLTAGGEVTYFMTGPEGEQYRGWWRITSVSPPTSLEFVDGFADQDGKPKDDMPTTAARVRLTAHGGGTRMELRWVFGSREQMERLVNMGMVEGLGQAVGQIDALLTG

Crispr_ID: NZ_LN831790_2

• CRISPR_ID: NZ_LN831790_2
• CRISPR_location: 2517229-2517398
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_LN831790_2

Consensus_repeat	Method
CGGCGGCCGGGGCCTCCTCGGCC	CRISPRCasFinder

spacers of NZ_LN831790_2

>2.1|2517252|16|NZ_LN831790|CRISPRCasFinder
TCGGCGGCCGGAGCCT
>2.2|2517291|28|NZ_LN831790|CRISPRCasFinder
GGAGCCTCGGCCGGCTTCTCGCCCTCGG
>2.3|2517342|34|NZ_LN831790|CRISPRCasFinder
TTCTTCTCGCCCTCGAGCAGGTCGCGCTCCCACT

CRISPR arrays and Neighbor proteins around NZ_LN831790_2

CRISPR arrays

The CRISPR arrays of NZ_LN831790_2

>merge|NZ_LN831790|2|2517229-2517398|CRISPRCasFinder
TGACGGGTCAGGCCTGCTCGGCCTCGGCGGCCGGAGCCTCGGCGGCCGGGGCCTCCTCGGCCGGAGCCTCGGCCGGCTTCTCGCCCTCGGCGGCGGCCGGGGCCTCGTCGGCCTTCTTCTCGCCCTCGAGCAGGTCGCGCTCCCACTCGGCGAGCGGCTCGCCCGCGGCC

>NZ_LN831790|2|2|2517229-2517398|CRISPRCasFinder
TGACGGGTCAGGCCTGCTCGGCC	TCGGCGGCCGGAGCCT
CGGCGGCCGGGGCCTCCTCGGCC	GGAGCCTCGGCCGGCTTCTCGCCCTCGG
CGGCGGCCGGGGCCTCGTCGGCC	TTCTTCTCGCCCTCGAGCAGGTCGCGCTCCCACT
CGGCGAGCGGCTCGCCCGCGGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029385525.1|2508147_2509167_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226361
NZ_LN831790.1|WP_029383621.1|2519227_2519785_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_LN831790.1|WP_029385527.1|2510815_2511892_-|thiamine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270263
NZ_LN831790.1|WP_029383620.1|2519893_2520736_-|RNA-polymerase-sigma-factor-WhiG	unknown	unknown	gnl|CDD|235770
NZ_LN831790.1|WP_078648322.1|2509169_2510840_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|224099
NZ_LN831790.1|WP_029383616.1|2524631_2525156_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|240041
NZ_LN831790.1|WP_029383619.1|2521005_2522160_-|DNA-protecting-protein-DprA	unknown	unknown	gnl|CDD|376794
NZ_LN831790.1|WP_029385534.1|2516242_2517079_-|elongation-factor-Ts	unknown	unknown	gnl|CDD|236491
NZ_LN831790.1|WP_029385531.1|2514532_2515090_-|ribosome-recycling-factor	unknown	unknown	gnl|CDD|178850
NZ_LN831790.1|WP_029385521.1|2506542_2507277_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_LN831790.1|WP_029385532.1|2515286_2516045_-|UMP-kinase	unknown	unknown	gnl|CDD|234735
NZ_LN831790.1|WP_029385528.1|2512128_2513235_-|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	unknown	unknown	gnl|CDD|184689
NZ_LN831790.1|WP_029385523.1|2507325_2508123_-|maleylpyruvate-isomerase-family-mycothiol-dependent-enzyme	unknown	unknown	gnl|CDD|274422
NZ_LN831790.1|WP_029383618.1|2522156_2523767_-|YifB-family-Mg-chelatase-like-AAA-ATPase	unknown	unknown	gnl|CDD|223679
NZ_LN831790.1|WP_029383617.1|2523766_2524129_-|YraN-family-protein	unknown	unknown	gnl|CDD|237119
NZ_LN831790.1|WP_018544766.1|2524267_2524576_-|DUF2469-domain-containing-protein	unknown	unknown	gnl|CDD|313765
NZ_LN831790.1|WP_029383615.1|2525145_2525922_-|signal-peptidase-I	unknown	unknown	gnl|CDD|274044
NZ_LN831790.1|WP_047121706.1|2518398_2518995_+|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_LN831790.1|WP_047121705.1|2513315_2514533_-|phosphatidate-cytidylyltransferase	unknown	unknown	gnl|CDD|366491
NZ_LN831790.1|WP_047121707.1|2526015_2526996_-|signal-peptidase-I	unknown	unknown	gnl|CDD|274044

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029385525.1|2508147_2509167_-|ABC-transporter-ATP-binding-protein	gnl|CDD|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	1.99065e-121
NZ_LN831790.1|WP_029383621.1|2519227_2519785_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	1.57193e-08
NZ_LN831790.1|WP_029385527.1|2510815_2511892_-|thiamine-ABC-transporter-substrate-binding-protein	gnl|CDD|270263	cd13545, PBP2_TbpA, Substrate binding domain of thiamin transporter, a member of the type 2 periplasmic binding fold superfamily. Thiamin-binding protein TbpA is the periplasmic component of ABC-type transporter in E. coli, while the transmembrane permease and ATPase are ThiP and ThiQ, respectively. Thiamin (vitamin B1) is an essential confactor in all living systems that most prokaryotes, plants, and fungi can synthesized thiamin. However, in vertebrates, thiamine cannot be synthesized and must therefore be obtained through dietary absorption. In addition to thiamin biosynthesis, most organisms can import thiamin using specific transporters. After binding thiamine with high affinity, TbpA interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The thiamine-binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	5.95054e-114
NZ_LN831790.1|WP_029383620.1|2519893_2520736_-|RNA-polymerase-sigma-factor-WhiG	gnl|CDD|235770	PRK06288, PRK06288, RNA polymerase sigma factor WhiG; Reviewed.	5.86537e-170
NZ_LN831790.1|WP_078648322.1|2509169_2510840_-|iron-ABC-transporter-permease	gnl|CDD|224099	COG1178, ThiP, ABC-type Fe3+ transport system, permease component [Inorganic ion transport and metabolism].	3.03375e-88
NZ_LN831790.1|WP_029383616.1|2524631_2525156_-|NUDIX-domain-containing-protein	gnl|CDD|240041	cd04685, Nudix_Hydrolase_26, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily requires a divalent cation, such as Mg2+ or Mn2+, for their activity and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	3.9173e-56
NZ_LN831790.1|WP_029383619.1|2521005_2522160_-|DNA-protecting-protein-DprA	gnl|CDD|376794	pfam02481, DNA_processg_A, DNA recombination-mediator protein A. The SMF family, of DNA processing chain A, dprA, are a group of bacterial proteins. In H. pylori, dprA is required for natural chromosomal and plasmid transformation. It has now been shown that DprA is found to bind cooperatively to single-stranded DNA (ssDNA) and to interact with RecA. In the process, DprA-RecA-ssDNA filaments are produced and these filaments catalyze the homology-dependent formation of joint molecules. While the E.coli SSB protein limits access of RecA to ssDNA, DprA alleviates this barrier. It is proposed that DprA is a new member of the recombination-mediator protein family, dedicated to natural bacterial transformation.	2.71253e-81
NZ_LN831790.1|WP_029385534.1|2516242_2517079_-|elongation-factor-Ts	gnl|CDD|236491	PRK09377, tsf, elongation factor Ts; Provisional.	1.30638e-124
NZ_LN831790.1|WP_029385531.1|2514532_2515090_-|ribosome-recycling-factor	gnl|CDD|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	1.45216e-104
NZ_LN831790.1|WP_029385521.1|2506542_2507277_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.05728e-07
NZ_LN831790.1|WP_029385532.1|2515286_2516045_-|UMP-kinase	gnl|CDD|234735	PRK00358, pyrH, uridylate kinase; Provisional.	3.71396e-136
NZ_LN831790.1|WP_029385528.1|2512128_2513235_-|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	gnl|CDD|184689	PRK14459, PRK14459, ribosomal RNA large subunit methyltransferase N; Provisional.	0
NZ_LN831790.1|WP_029385523.1|2507325_2508123_-|maleylpyruvate-isomerase-family-mycothiol-dependent-enzyme	gnl|CDD|274422	TIGR03083, TIGR03083, uncharacterized Actinobacterial protein TIGR03083. This protein family pulls together several groups of proteins, each very different from the others. They share in common three conserved regions. The first is a region of about 38 amino acids, nearly always at the N-terminus of a protein. This region has a bulky hydrophobic residue, usually Trp, at position 29, and a His residue at position 37 that is invariant, so far, in over 150 instances. The second conserved region has a motif [DE]xxxHxxD. The third conserved region contains a hydrophobic patch and a well-conserved Arg residue. Most examples are found in the Actinobacteria, including the genera Mycobacterium, Corynebacterium, Streptomyces, Nocardia, Frankia, etc. The pattern of near-invariant residues against a backdrop of extreme sequence divergence suggests enzymatic activity and conservation of active site residues.	4.42099e-14
NZ_LN831790.1|WP_029383618.1|2522156_2523767_-|YifB-family-Mg-chelatase-like-AAA-ATPase	gnl|CDD|223679	COG0606, COG0606, Predicted ATPase with chaperone activity [Posttranslational modification, protein turnover, chaperones].	1.2967e-178
NZ_LN831790.1|WP_029383617.1|2523766_2524129_-|YraN-family-protein	gnl|CDD|237119	PRK12497, PRK12497, YraN family protein.	9.68999e-41
NZ_LN831790.1|WP_018544766.1|2524267_2524576_-|DUF2469-domain-containing-protein	gnl|CDD|313765	pfam10611, DUF2469, Protein of unknown function (DUF2469). Member proteins often found in Actinomycetes clustered with signal peptidase and/or RNAse-HII.	2.27317e-62
NZ_LN831790.1|WP_029383615.1|2525145_2525922_-|signal-peptidase-I	gnl|CDD|274044	TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].	1.27743e-46
NZ_LN831790.1|WP_047121706.1|2518398_2518995_+|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	1.61013e-20
NZ_LN831790.1|WP_047121705.1|2513315_2514533_-|phosphatidate-cytidylyltransferase	gnl|CDD|366491	pfam01148, CTP_transf_1, Cytidylyltransferase family. The members of this family are integral membrane protein cytidylyltransferases. The family includes phosphatidate cytidylyltransferase EC:2.7.7.41 as well as Sec59 from yeast. Sec59 is a dolichol kinase EC:2.7.1.108.	2.28399e-78
NZ_LN831790.1|WP_047121707.1|2526015_2526996_-|signal-peptidase-I	gnl|CDD|274044	TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].	1.40734e-41

Protein sequences

>NZ_LN831790.1|WP_029385534.1|2516242_2517079_-|elongation-factor-Ts
MANYTAADVKKLRELTGAGMMDCKKALDEAEGNVDKAVEALRIKGQKGVAKREGRSAENGAVVSIIADDNSSGVLVELKCETDFVAKGEKFQAVANAIAEHVTKTSPADIEALLASEIEPGKTVQAFVDEANANLGEKIVLDRFAQFSDGYVTAYMHRTMPDLPPQIGVLVELDKANAEVAKGVAQHIAAFAPKYLSKEDVPADVVEAERRIAEETTRAEGKPEAALPKIVEGRLNGFFKDATLLGQPYALDNKKSVQKVLDEAGVTLKRFTRIKVGI
>NZ_LN831790.1|WP_029385532.1|2515286_2516045_-|UMP-kinase
MTTKADKSDDGKVRGRFLLKLSGEAFSGGGGLGVDPDVVHAIAREIAAVVRDGAQIAIVIGGGNFFRGAELQVRGMDRARSDYMGMLGTVMNCLALQDFLEKEGVDCRVQTAITMGQVAEPYIPLRAVRHLEKGRVVIFGAGMGMPYFSTDTTAAQRALEIDAEALLMGKNGVDGVYDSDPKTNPDAVKFDALGYGEVITRDLKVADATAITLCRDNRLPIVVFELLKEGNIARAVKGEKIGTLVGDEGSRD
>NZ_LN831790.1|WP_029385531.1|2514532_2515090_-|ribosome-recycling-factor
MIEETLLEAEEKMEKAVVVAKEDFAAIRTGRAHPAMFNKIVADYYGAPTPINQLASFSVPEPRMAVVTPFDKSALRNIEQAIRDSDLGVNPSNDGNIIRVVFPELTEERRREYIKVAKSKGEDAKVSIRSVRRKAKDAIDKLVKDGEVGEDEGRRAEKELDDTTAKYVAQVDELLKHKEAELLEV
>NZ_LN831790.1|WP_047121705.1|2513315_2514533_-|phosphatidate-cytidylyltransferase
MNDSSWGAPPQAGYWEPTDRGPARGAAPAGPAYDAQHAQQTRPMPIVPDVPEHGGDQDDDRGAARLSGPLFRDGTPRPQPYGTPRPQPYGPPRTDLYDAPQPRPHDTPQAPPFGAVPQNPEPMPDAPQPAPPQKKSAGRDLGAAIGVGVGLGAVIVASLFIVKAVFVGVIAVAVVVGLWELTRRLQERKGIKAPLVPLAVGGAAMVVAGYVRGPEAAWVAMALTALAVLVWRMTEPPEDYLKDVTAGVFAAFYVPFLATFVALMLTADDGPFRVLTFLLLTVVSDTGAYAVGWRFGRKKLAPRISPGKTREGLLGAVAFAMAVGALCLEFLIDGGAWWQGLLLGLAVAVSATLGDLGESMIKRDLGIKDMGSLLPGHGGIMDRLDSLLPTAPVVWLLLVVFVGTS
>NZ_LN831790.1|WP_029385528.1|2512128_2513235_-|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN
MPKPGELTFVAPRGAKKPPRHLADLTPAERKEAVAAIGEKPFRAKQLSQHYFARYAHDPEQWTDIPAGSRGKLQEALLPELMTVVRHLSTDQGTTRKTLWRLFDGTLVESVLMRYPDRVTMCISSQAGCGMNCPFCATGQAGLDRNLSTAEIVHQIVDGMRALRDGEVPGGPARLSNIVFMGMGEPLANYNRVVGAIRRLTDPEPDGVGLSQRGITVSTVGLVPAIHRFADEGFKCRLAISLHAPDDELRDTLVPVNTRWKVREVLDAGFEYAAKSGRRLSIEYALIRDINDQAWRGDRLGRLLKGRPVHVNLIPLNPTPGSQWTASRPEDEKAFVEAIAAHGVPVTIRDTRGQEIDGACGQLAASER
>NZ_LN831790.1|WP_029385527.1|2510815_2511892_-|thiamine-ABC-transporter-substrate-binding-protein
MSITKKATILAVGLGLVTLSACGSSGGGGESGDSRTVTLVSHDSWAASKEVIAAFEKESGYRVRVLKDGDAGQAVNKAILTKDNPQGDVLFGVDNTLLSRALDNGLFQPYEAKDADRVRPEYRADQDRHRVTPVDTGDICVNYDKEWFSEHKLTPPASFDDLIEPRYKNLLVTENAATSSPGLGFLLGTAARYGDGWPEYWKKLKANGVKVVDGWEQAYNEEFSGSAAGRKAKADRPLVVSYASSPPAEVIYADPRPDTAPTGIAPGTCFRQVEYAGLLNNARNPEGGKALLDFLIGKRFQDDMPLNMFVYPVRDDAKVPADFARFGPQAENPQTMDPDEIAGHRDEWVKSWTSLVLK
>NZ_LN831790.1|WP_078648322.1|2509169_2510840_-|iron-ABC-transporter-permease
MDLARSEVAVRGRRRGSAARLALMAGPVAFFAVFFAYPVVAIVGRGLKDGDGWHLARIGQVLADPGVRHVLWFTTWQALVSTALTLLIALPGAYVFARLDFPGKQVLRAVVTVPFVLPTVVVGTAFLALAGRGGLLDELWGVRLDTTVWAILLAHVFFNYAVVVRTVGGLWAQLDPRQEEAARMLGASRPAAWRTITLPALAPAVAAAALMVFLFTFTSFGVVQILGGPTFATLEVEIYRQTADVFDLSTAAVLTMIQFVAVGAILAVHAWTVRRRETALRLVDASLTARRPRGAGQWALLAGVLVTVAVLLVLPLAVLVERSLDAPGFASYRALTSADSGVFLVPPIEAIGTSLQYAVVATAIAVVIGGLAATALTRRDAGRLVRGFDALLMLPLGVSAVTVGFGFLIALDQPPLDLRSAWILVPLAQALVGVPFVVRTMLPVLRAVDTRLREAAAVLGASPWRVWREVDLPLVRRALLVAAGFAFAVSLGEFGATVFIARPDNPTLPVAVARLLGRPGETNYGQSMALSTILMVVCAVALLVLERLRTDRTGEF
>NZ_LN831790.1|WP_029385525.1|2508147_2509167_-|ABC-transporter-ATP-binding-protein
MLLSLRGATVRFGGRAVLDAVDLDVAEHEIVCVLGPSGSGKSTLLRAVAGLQPLDAGAVLLGGRDQAGVPAHRREVGLMFQDHQLFPQRDVGGNVAFGLRTRGVPRAERSERVAELLELVGLPGAARRAVAALSGGEQQRVALARALAPRPRLLMLDEPLGQLDRSLRERLVVELRELFGRLGTTVLAVTHDQGEAFALADRVVVMREGRIAQSGTPLEVWQRPADAFVARFLGFENVVEAAVTGQAADTPWGKVPVPEDAPQGARSLLVRPAGVRLVPVGEGLRCTVAARTFRGTHVAVRLQPGDAPPLEAACALRSAPETGDEVGVEFDPAEIVVLG
>NZ_LN831790.1|WP_029385523.1|2507325_2508123_-|maleylpyruvate-isomerase-family-mycothiol-dependent-enzyme
MTLLAHDRYCDEITEQVRLFRAVITSGADLSATVPTCPDWTLEELVRHTGRALRWVELLVRTRAREDIPMEQVPGADGPRARGDAAALDAWLATSGEAVAAVLREAGPDTKVWTWSGTHTTGFWARRMTHELVVHRADAALAAGQPFEVGPEVAADAIDEWLETVRFMQRVLPDAPVGELRGPGRSLHLHATDTAPGLNAEWLIELTGDGIAWRRGHEKATVALRGPLTPLLLAFYRRLPVETPGLEVLGERELLDLWLERASFG
>NZ_LN831790.1|WP_029385521.1|2506542_2507277_+|hypothetical-protein
MAVLSFLSRPASRRGLIRPARVLGVAAASAALAAGAAGTALACDIGEFTAAAKCDGGKGVITVTDADPSGVPATVTVFLRGDGADEKIGEQVVKGSREGTTIVFTEDWKPNAEYRVHVEAAGYVDEDIEPHLVTPATACAPQETPAPAPTPTPTPTPSRSASAPAGESGAPAPAPSSPAASASQSSAPAGGADNAPSPAGEAGLAETGGGSNTGLIAGVAAGLVVIGGGAVFLGMRRRGSKNDR
>NZ_LN831790.1|WP_047121706.1|2518398_2518995_+|M23-family-metallopeptidase
MRLRRCVHPGTWPALLAALLLTPALVPGPAPAAVAADGGRPAGPAVPAVGRAWPVGVRPPVLRGWDPPPGPYAPGHRGVDLAAAPGTPVRAVAPGRVSFAGRVAGKGVVSVELAGTGEPPLRTTYEPVRASVRAGETVAAGEVVGTVEPAGSHCAAPCLHWGLRGENAYLNPLTLLPPWLLRTGPSRLLPVLGVPLPP
>NZ_LN831790.1|WP_029383621.1|2519227_2519785_-|TetR/AcrR-family-transcriptional-regulator
MAEHRSMQRAALLDAARSLLSEGGTEALTFPALAERTGLARSSVYEYFRSRAAVVEELCAVDFPLWAAEVEAAMAAVDGPEAKVEAYVRKQLELVGDRRHRAVVAISASELDAGAREKIRAAHGGLIAMIVEALGEMGHAQPRLAAMLLQGVVDAAVRRIELGAAEDPASVTDAAVSMALRGVRG
>NZ_LN831790.1|WP_029383620.1|2519893_2520736_-|RNA-polymerase-sigma-factor-WhiG
MPQHTSGSDRAAIPPAARDGGSVRPPAPSTLDELWRSYKATGDERLREQLILHYSPLVKYVAGRVSVGLPPNVEQADFVSSGVFGLIDAIEKFDIDREIKFETYAITRIRGAMIDELRALDWIPRSVRQKARNVERAYATLEARLRRTPTESEVAAEMGIAVEELHSVFSQLSLANVVALEELLHVGGEGGGRLSLMDTLEDTAADNPVEVAEDRELRRFLARAINTLPDREKTVVTLYYYEGLTLAEIGNVLGVTESRVSQIHTKSVLQLRAKLAGFGR
>NZ_LN831790.1|WP_029383619.1|2521005_2522160_-|DNA-protecting-protein-DprA
MSAGADPDLLDRVFLTRVIEPGDETGGRWVREHGVREVARRLRADGPALPGVSVQRWAGLRARAGRADPQGDLAAAEAAGVRFVCPGTVEWPAQLDDLGAARPLGLWVRGGPDLRMWALRSVAVVGARACTEYGAHMAATLAAGLAERGWVVISGGAYGIDGAAHRGALGAGGATVAVLACGVDRPYPRGHTGLITRIAGQGLVVGELPPGEHPTPSRFILRNRVIAALTRGTVVVEAAHRSGSLATARAAQRLGRHTMGVPGPATSGLSAGVHELLRGGAALVTDAADVVELVGAMGELAPERRGPVLPTDLLSGPARQVLAALPASRAAPPSEIARDARTTEDDAIARLYELRALGYVERHDDGWKLTRQAVSSSRARRPPC
>NZ_LN831790.1|WP_029383618.1|2522156_2523767_-|YifB-family-Mg-chelatase-like-AAA-ATPase
MGFARTCSVALVGVEGVVVEVQADLEPGVAAFTLVGLPDKSLSESRDRVRAAVVNSGAEWPQKKLTVGLSPASVPKAGSGYDLAVASAVLGAAERIDPRVLTDIVMIGELGLDGRVRPVRGILPAVLAAADAGFEQVVVPECAAAEASLVPGVSVLGVRTLRQLIAVLADEPVPEEEPDEPDRPDPLAAGLRLPGGMHAVGAAQPDHGHDLADVVGQLSARTAVEVAAAGGHHLFLEGPPGAGKTMLAERLPAILPRLGRQESLEVTAVHSVAGLLPPGKPLIDTAPYCAPHHSATMQALVGGGPGIARPGAVSLAHQGVLFLDETPEFSSHVLDALRQPLEAGHVVIARSAGVVRFPAKFLMVLAANPCPCGRFSQQENLCECPPSAIRRYQARLSGPLLDRVDLRVEVDRVTRAELSGRGARGESTATVAARVRAARERAGARLAGTPWRSNSEVPGRELRRRWPAAPGAMDEAERSLERGVLTARGLDRVLRVAWTVADLAGHDRPDATDVALALQLRTGVPRGVPMAIGARA
>NZ_LN831790.1|WP_029383617.1|2523766_2524129_-|YraN-family-protein
MNARGALGRYGEDLAARRLSEAGMTVLERNWRCGRAGEIDIVARDGDVLVFCEVKTRRSGRFEHPMAAVRPEKAERLRRLAERWIQTHGAAPPGGARIDLIGVVLPERGAPVVEHARGVA
>NZ_LN831790.1|WP_018544766.1|2524267_2524576_-|DUF2469-domain-containing-protein
MSAEDLEKYETEMELKLYREYRDVVGLFKYVIETERRFYLTNDYEMQVHSVQGEVFFEVTMADAWVWDMYRPARFVKQVRVLTFKDVNIEELNKSDLELPSG
>NZ_LN831790.1|WP_029383616.1|2524631_2525156_-|NUDIX-domain-containing-protein
MSAETTGAGQDTYEGGLRKVARVVLLDPRDRILLLHGHEPDDPADDWWFTPGGGVEGDETRDQAALRELAEETGITDVELGPVLWRRRCSFPFAGRRWDQDEWYYLARTTQTATVAAGLTELERRSVAGARWWTCEELARAHETVYPNRLAELLRTLLDEGPPAGPVTLDPEIV
>NZ_LN831790.1|WP_029383615.1|2525145_2525922_-|signal-peptidase-I
MGGESTTHTAPRGGGVNTGPAGGGTGQRLSGLAVALGLVLFLGGFVWAAVVYRPYTVPTRSMAPTIDAGDRVLAQRVGGGEVRRGDVVVFEDATWSNAPMVKRVVAVGGDTVSCCQDGKLTVNGKQIDEPYLPEGSAAEAGPFPTVTVPKGRLFLLGDERGSSLDSTAHLTEAAQGTVASGAVEARVDAVVWPMDGMLQRPSGFEELGALSSPGPLRTMVAMVAAGTVLIFGGAAYGPLAGRAAASRARSRTESAGVR
>NZ_LN831790.1|WP_047121707.1|2526015_2526996_-|signal-peptidase-I
MAVGARSGHDGEEHRGRPVETAGSAGTPAAPGSRTMAEDGRVTGEQTGGHDEDQGPVGQRTPKEARKQRSFWKELPILIGVALVLALLIKTFLVQAFSIPSDSMQNTLQQGDRVLVDKLTPWFGSEPERGEVVVFHDPDNWLAGEPTIDPNPLQEFLSWIGLMPSAEEKDLIKRVIGVGGDTVECKGTGPVRVNGKALDDRDFVYPGNTPCSVDDNGGQFKVKVPEGYIWVMGDHRQNSRDSRYNQADRYHGMVPVNEVVGRAIVIAWPVNRWDTLPVPDTFDQPGLNAGAAAAGALSVAPQGLALAGVVPVALWRRRRTAPAGNR

Crispr_ID: NZ_LN831790_3

• CRISPR_ID: NZ_LN831790_3
• CRISPR_location: 2584114-2584214
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_3

Consensus_repeat	Method
GTGGTCTTCTTCGCCGCGCCCGTGGTCTTCTTCGC	CRISPRCasFinder

spacers of NZ_LN831790_3

>3.1|2584149|31|NZ_LN831790|CRISPRCasFinder
CGCGCCCGTGGTCTTCTTCGCCGCCGCGGCG

CRISPR arrays and Neighbor proteins around NZ_LN831790_3

CRISPR arrays

The CRISPR arrays of NZ_LN831790_3

>merge|NZ_LN831790|3|2584114-2584214|CRISPRCasFinder
GCGGTCTTCTTCGCCGTGGCGGTGGTCTTCTTCGCCGCGCCCGTGGTCTTCTTCGCCGCCGCGGCGGTGGTCTTCTTCGCCGCGGCCGTGGTCTTCTTCGC

>NZ_LN831790|3|3|2584114-2584214|CRISPRCasFinder
GCGGTCTTCTTCGCCGTGGCGGTGGTCTTCTTCGC	CGCGCCCGTGGTCTTCTTCGCCGCCGCGGCG
GTGGTCTTCTTCGCCGCGGCCGTGGTCTTCTTCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029384507.1|2584746_2584977_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029384501.1|2589790_2590492_-|DUF4241-domain-containing-protein	unknown	unknown	gnl|CDD|379427
NZ_LN831790.1|WP_047121714.1|2575739_2576969_+|FAD-dependent-monooxygenase	unknown	unknown	gnl|CDD|169028
NZ_LN831790.1|WP_029384515.1|2581022_2582033_-|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase	unknown	unknown	gnl|CDD|234629
NZ_LN831790.1|WP_029384506.1|2585243_2585837_-|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl|CDD|179314
NZ_LN831790.1|WP_029384514.1|2582029_2582803_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_LN831790.1|WP_029384512.1|2582959_2583610_+|2-phospho-L-lactate-guanylyltransferase	unknown	unknown	gnl|CDD|274643
NZ_LN831790.1|WP_029384517.1|2579794_2580952_-|D-alanine--D-alanine-ligase	unknown	unknown	gnl|CDD|234993
NZ_LN831790.1|WP_029384522.1|2577746_2578715_-|thiamine-phosphate-kinase	unknown	unknown	gnl|CDD|235583
NZ_LN831790.1|WP_078648180.1|2593142_2593331_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029384510.1|2583619_2583823_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029384504.1|2585843_2587271_-|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl|CDD|235490
NZ_LN831790.1|WP_029384519.1|2579277_2579769_+|DUF3515-domain-containing-protein	unknown	unknown	gnl|CDD|378794
NZ_LN831790.1|WP_047121715.1|2593934_2597666_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|377989
NZ_LN831790.1|WP_029384502.1|2588988_2589720_-|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223943
NZ_LN831790.1|WP_078648271.1|2590664_2592146_-|glutamate--tRNA-ligase	unknown	unknown	gnl|CDD|234953
NZ_LN831790.1|WP_023546516.1|2587468_2588185_+|IclR-family-transcriptional-regulator-NdgR	unknown	unknown	gnl|CDD|224332
NZ_LN831790.1|WP_029384499.1|2592138_2592924_-|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_LN831790.1|WP_029384523.1|2576943_2577750_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	unknown	unknown	gnl|CDD|180561
NZ_LN831790.1|WP_029384521.1|2579023_2579257_+|Lrp/AsnC-ligand-binding-domain-containing-protein	unknown	unknown	gnl|CDD|366431

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029384501.1|2589790_2590492_-|DUF4241-domain-containing-protein	gnl|CDD|379427	pfam14025, DUF4241, Protein of unknown function (DUF4241). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 205 and 315 amino acids in length. There is a conserved GDG sequence motif at the C-terminus.	2.36016e-59
NZ_LN831790.1|WP_047121714.1|2575739_2576969_+|FAD-dependent-monooxygenase	gnl|CDD|169028	PRK07588, PRK07588, FAD-binding domain.	4.83439e-93
NZ_LN831790.1|WP_029384515.1|2581022_2582033_-|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase	gnl|CDD|234629	PRK00094, gpsA, NAD(P)H-dependent glycerol-3-phosphate dehydrogenase.	1.05132e-180
NZ_LN831790.1|WP_029384506.1|2585243_2585837_-|3-isopropylmalate-dehydratase-small-subunit	gnl|CDD|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	2.27433e-127
NZ_LN831790.1|WP_029384522.1|2577746_2578715_-|thiamine-phosphate-kinase	gnl|CDD|235583	PRK05731, PRK05731, thiamine monophosphate kinase; Provisional.	7.76626e-132
NZ_LN831790.1|WP_029384512.1|2582959_2583610_+|2-phospho-L-lactate-guanylyltransferase	gnl|CDD|274643	TIGR03552, F420_cofC, 2-phospho-L-lactate guanylyltransferase. Members of this protein family are the CofC enzyme of coenzyme F420 biosynthesis. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	1.70419e-43
NZ_LN831790.1|WP_029384517.1|2579794_2580952_-|D-alanine--D-alanine-ligase	gnl|CDD|234993	PRK01966, ddl, D-alanine--D-alanine ligase.	2.25497e-178
NZ_LN831790.1|WP_047121715.1|2593934_2597666_+|sensor-histidine-kinase	gnl|CDD|377989	pfam08376, NIT, Nitrate and nitrite sensing. The nitrate- and nitrite sensing domain (NIT) is found in receptor components of signal transducing pathways in bacteria which control gene expression, cellular motility and enzyme activity in response to nitrate and nitrite concentrations. The NIT domain is predicted to be all alpha-helical in structure.	1.28196e-36
NZ_LN831790.1|WP_029384514.1|2582029_2582803_-|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.	7.63583e-45
NZ_LN831790.1|WP_029384504.1|2585843_2587271_-|3-isopropylmalate-dehydratase-large-subunit	gnl|CDD|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_LN831790.1|WP_029384519.1|2579277_2579769_+|DUF3515-domain-containing-protein	gnl|CDD|378794	pfam12028, DUF3515, Protein of unknown function (DUF3515). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 166 to 214 amino acids in length. This protein has a conserved RCG sequence motif.	9.1229e-23
NZ_LN831790.1|WP_029384502.1|2588988_2589720_-|HAD-family-hydrolase	gnl|CDD|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	9.85593e-36
NZ_LN831790.1|WP_078648271.1|2590664_2592146_-|glutamate--tRNA-ligase	gnl|CDD|234953	PRK01406, gltX, glutamyl-tRNA synthetase; Reviewed.	0
NZ_LN831790.1|WP_023546516.1|2587468_2588185_+|IclR-family-transcriptional-regulator-NdgR	gnl|CDD|224332	COG1414, IclR, Transcriptional regulator [Transcription].	7.76445e-46
NZ_LN831790.1|WP_029384499.1|2592138_2592924_-|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	2.96489e-101
NZ_LN831790.1|WP_029384523.1|2576943_2577750_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	gnl|CDD|180561	PRK06427, PRK06427, bifunctional hydroxy-methylpyrimidine kinase/ hydroxy-phosphomethylpyrimidine kinase; Reviewed.	2.58098e-122
NZ_LN831790.1|WP_029384521.1|2579023_2579257_+|Lrp/AsnC-ligand-binding-domain-containing-protein	gnl|CDD|366431	pfam01037, AsnC_trans_reg, Lrp/AsnC ligand binding domain. The l-leucine-responsive regulatory protein (Lrp/AsnC) family is a family of similar bacterial transcription regulatory proteins. The family is named after two E. coli proteins involved in regulating amino acid metabolism. This entry corresponds to the usually C-terminal regulatory ligand binding domain. Structurally this domain has a dimeric alpha/beta barrel fold.	9.69143e-09

Protein sequences

>NZ_LN831790.1|WP_029384510.1|2583619_2583823_+|hypothetical-protein
MQATAYTYDPDSRSGQVLLDDGTPVPFDAAAFDAGGLRLLRPGQRVRIETEGEGAGRRITLVTLQTF
>NZ_LN831790.1|WP_029384512.1|2582959_2583610_+|2-phospho-L-lactate-guanylyltransferase
MQWTLVVPVKHLARAKSRLSDTADDGMRPGLALAFALDTVTAALACPEVADVAVVTDDARAGRELAALGAAVVPDEPGGGLNAALAHAAAVVRAARPGRPVATLNADLPALRPAELARVLQEAAQFPRAFLADAAAIGTTVLAAAPGQSLRPAFGPDSRARHRASGAAELRLDAVDSVRQDVDTGDDLRAALALGVGPHTAAAAALLPGRAPVPGQ
>NZ_LN831790.1|WP_029384514.1|2582029_2582803_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MPRRRIGFWYRFAAVICKPPLVVLLKRDWRGMEHIPAEGGFITVVNHNSHIDPFAYAHFQYNTGRVPRFLAKSGLFRKGFVGAAMRGTGQIPVYRESTDALSAFRAAIDAVERGECVAFYPEGTLTRDPDGWPMTGKTGAARVALQTRCPVIPVAQWGCNEVLPPYAKKPNLFPRKTHRVLAGPPVDLSRFYGKEMTADVLKEATEVIMAAITRQLEEVRGEKAPDTPYDPRRERIEQRRRTQAQRQRRRQAEGQGT
>NZ_LN831790.1|WP_029384515.1|2581022_2582033_-|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase
MREPVKAAVFGTGSWGTAFAMVLADAGCEVTLWGRRAELAEAVNSTRTNPDYLPGVELPGNVRATTDAAEAARDADFTVLAVPSQTLRGNLAAWAPLLAPGTVLVSLMKGIELGSAMRMSEVIEDVAAVGRDRIAVVSGPNLAREIAARMPAASVVACTDEAVARRLQTACHTPYFRPYTNTDVVGCELGGAVKNVIGLAVGIADGMGLGDNAKGSLITRGLAETTRLGVALGADPLTFSGLAGLGDLVATCSSPLSRNHTFGTNLGKGMTLQETIAVTRQTAEGVKSCESVLDLARRHGVDMPITETVVGIVHESKPPVVALKELMSRSAKPERR
>NZ_LN831790.1|WP_029384517.1|2579794_2580952_-|D-alanine--D-alanine-ligase
MSTENLPQSPGQPTRKPRVAVVFGGRSSEHGISAVTAGAVLKAIDRTKYDVLPIGITRDGRWALTADEPERMVITERRTPSVEDLAESTEGSVVLSVDPGSREVVYSEPGSVPKVLGEVDVVFPVLHGPYGEDGTLQGLLELSGVPYVGSGVLASAVGQDKEYMKRVFTSFGLAVGPYVVIRPREWQQDVSAARKKIVDFAGEHGWPLFVKPARAGSSIGITKVDDLSGLDEAIEEARRHDPKILVEAALRGREIECGVLEFEDGPRASVPAEIPPPEAHAYYDFEAKYIDSTPGIVPAPLTPEETAEVQRLAVEAFEAASCEGLVRADFFLTEDGEFVINEINTMPGFTPISMYPQMWQAGGVSYPELVDRLVQAALRRSTGLR
>NZ_LN831790.1|WP_029384519.1|2579277_2579769_+|DUF3515-domain-containing-protein
MNSFPHRHRFVLAPPALGLLLAAAGCSSADGSASAAVPSPGADATRLCRNLDAELPSKVDGLSREDPEPRSALTAGWGNPVIILRCGVPRPAEMSDPEADGVEVDGVGWLLQKRKDGSFRFTTTLRKAYAEVTLPKERAGDGLAPLVDLAPAVKKAIPEGIAD
>NZ_LN831790.1|WP_029384521.1|2579023_2579257_+|Lrp/AsnC-ligand-binding-domain-containing-protein
MVQAYILIQTEVGKASTVAETIGKIPGVIQAEDVTGPYDVIVRAQADTVDDLGRMVVAKVQQVDGITRTLTCPVVHL
>NZ_LN831790.1|WP_029384522.1|2577746_2578715_-|thiamine-phosphate-kinase
MKGTVGELGEFGLIRELTSRLTTTPAVRLGPGDDAAVVAAPDRRVVASTDILVEGRHFRRDWSTAYDVGRKAAAQNLADISAMGAVPTALLLGLVVPAELPVTWTTELMDGLRDECQVAGAAVVGGDVVRGDTITVSITALGDLRGQEPVTRGGARPGDLVAVTGWLGWSAAGYAVLSRGFRSPRAFVEAHRRPEPPYHAGPAAAALGATAMCDVSDGLIADLGHIAEASNVRIDIRSGQIDIPTQMNDIGQAVGVDPMQWVLTGGEDHAIVATFRPDVKLPARWKVIGEVLNPSALPQVTVDGAPWTSKGGWDHFGEDIES
>NZ_LN831790.1|WP_029384523.1|2576943_2577750_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase
MSALPRVLTVAGSDSGGGAGIQADLKTMLALGVHGMSVITAVTAQNSLGVQGAWELPVEAVREQYRSVVGDIGVQAVKTGMLASAELVETVAELIAGTDAPAVVDPVGVSKHGDALLAVSALDSVRTKLLPVATVATPNLDEVAQLTGVRVESEPDLRRAAAAVLEYGPRWALIKGGHLPGEAVDLLTDGSEEHWLRAPRHDNRHTHGTGCTLASAIASELAKGRSVPEAVTAAKQYVTGAIAAGFPLGGGIGPVDHGWMFRPGSPAA
>NZ_LN831790.1|WP_047121714.1|2575739_2576969_+|FAD-dependent-monooxygenase
MTDTTRTTRTPRAHRLGHLSVLVSGAGVAGPALALNLARHGARVTVVEKAPALREGGFAVDFRGHVHRTVLTSMGLWEEIHAHRTRMGRQTVVDADGTPRLDLPAQLMSGDVEITRGDLARIMYERTKDSAEYVFGDSVATLTEVPEGVDVTFEHGAPRRFDLVVGADGLHSHTRRLVFGDESRFLRFLGHYVAGFTVPNHLGLHGTGRLYSEPGRCVALSNCDGDPDLAGALLVFRSEPLSYDRRDVAAQKRMLAERFAGMGWETPAVLDALEGAGDLYFDAIAQIHADRLAQGRVALLGDAGYGATMGGMGTGVAIVGAHVLAGELALAGGDHRVAFARYERRIGGFARGCQKISGNVGPFFAPPTERRIRGRDRMYRLLASRPMAGSFKRLTEKAATAIKLPDYPA
>NZ_LN831790.1|WP_029384507.1|2584746_2584977_-|hypothetical-protein
MEHDGQLELYTAVAVQLKEAHARVRALQVPEGVRVALTRKLLVITAAAKHDLAGAARRLERFSADLDEGRFPEEER
>NZ_LN831790.1|WP_029384506.1|2585243_2585837_-|3-isopropylmalate-dehydratase-small-subunit
MEAFTTHTGRAVPLRRSNVDTDQIIPAHWLKKVTRDGFEDGLFEAWRKDPEFVLNRPERQGATVLVAGPDFGTGSSREHAVWALQNYGFKAVISSRFADIFRGNSLKNGLLTVVLDQKIVDSLWELTEADPTAEVTVDLVGREVRAAGITASFELDENSRWRLLNGLDDISITLQNEADIAAYEAKRPAYKPRTLQV
>NZ_LN831790.1|WP_029384504.1|2585843_2587271_-|3-isopropylmalate-dehydratase-large-subunit
MGRTLAEKVWDDHVVRRAEGEPDLLYIDLHLLHEVTSPQAFDGLRKSGRTVRRLDLTIATEDHNTPTLDIDKPIADPVSRVQLETLRKNCAEFGVRLHPLGDVEQGVVHVVGPQLGLTQPGTTVVCGDSHTSTHGAFGALAFGIGTSQVEHVLATQTLPMARPKTMAITVDGELPDGVTAKDLILAIIAKIGTGGGQGYILEYRGEAIEKLSMEARMTICNMSIEAGARAGMIAPDETTFAYLKGRPHAPEGADWDAAVEYWKTLRTDDDAEFDAEVVIEAAELSPFVTWGTNPGQGAPLSASVPDPASYEDASERLAAEKALEYMGLEAGQPLRSIKVDTVFVGSCTNGRIEDLRAAADILKGRKVADGVRMLVVPGSARVGLQAVSEGLDVVFKEAGAEWRHAGCSMCLGMNPDQLAPGERSASTSNRNFEGRQGKGGRTHLVSPQVAAATAVLGHLASPADLSADAPSPAGV
>NZ_LN831790.1|WP_023546516.1|2587468_2588185_+|IclR-family-transcriptional-regulator-NdgR
MDNSSGVGVLDKAALVLSALESGPATLAGLVGATGLARPTAHRLAVALEHHRMVARDMQGRFILGPRLAELAAAAGEDRLLATAGPVLTHLRDVTGESAQLYRRQGDMRICVAAAERLSGLRDTVPVGSTLTMKAGSSAQILLAWEEPERLHRGLQGARFTATALSGVRRRGWAQSIGEREPGVASVSAPVRGPSNRVVAAVSVSGPIERLTRHPGRMHAQAVIDAAARLSEALRRSG
>NZ_LN831790.1|WP_029384502.1|2588988_2589720_-|HAD-family-hydrolase
MAIRAVVWDVDDTLFDYTTADRAGMRAHLAAEGLLDGYGSAERALARWREITEVQWARFAAGEVDFATQRRDRTRVFLGRDLTDAEADGWFERYLAHYEAAWALFPDVLPVLDALATSHRHAVLSNSSVTVQDRKLRVLGLHDRFEIILCAAEIGISKPAAGAFLAACDALGLAPHEVAYVGDHPEIDGRGAADAGLLSVWIDRGGPRATAVPPAGPRRIASLAELPALLGPDTRFGAPSTFG
>NZ_LN831790.1|WP_029384501.1|2589790_2590492_-|DUF4241-domain-containing-protein
MPMSAPDYTWLFTPGSTFAYESGTTGVIHVASGGELWLPTGRIVACDPFVCLGEGETEPFTVAVEPGRYRVEAAVATLTQPGEPPSDEPHLRVAAARLVIRDEPTATWELALLPGQDPAELGDEEFYGYGVDAGTGCFYDAAAEESFPASEGDEGPLWDAFEHSDWAPGPHLITAPETGHTVVAFTSGWGDGAYPTWIGRTAAGEITCFVTDFFVAPDPSESAEPPAPATATA
>NZ_LN831790.1|WP_078648271.1|2590664_2592146_-|glutamate--tRNA-ligase
MASAPGSVRVRFCPSPTGNPHVGLVRTALFNWAFARHHGGTLVFRIEDTDAARDSEESYNQLLDSMRWLGFDWDEGPEIGGPHAPYRQSQRMDLYKEVAQKLLDGGYAYHCYCSQEELDTRREAARAAGRPSGYDGHCRELSAARVEEYKAQGREPIVRFRMPDETITFTDLVRGELTFTPENVPDYGIVRANGAPLYTLVNPVDDALMEITHVLRGEDLLSSTPRQIALYKALIELGIAQRIPEFGHLPYVMGEGNKKLSKRDPQSSLNLYRERGFLPEGLLNYLSLLGWSLSADQDVFTIDEMVAAFDVADVNPNPARFDLKKCEAINGDHIRMLEVKDFAERCRPWLKAPFAPWAPEDFDEAKWQAIAPHAQTRLKVLSEITDNVDFLFLAEPVEDEASWNKAMKEGSDALLRTAREKLEAADWTSPESLKEAVLAAGEAHGLKLGKAQAPVRVAVTGRTVGLPLFESLEILGKEKSLARIDAALAKLAA
>NZ_LN831790.1|WP_029384499.1|2592138_2592924_-|fumarylacetoacetate-hydrolase-family-protein
MRIARFSIDGNVAFGAVEGDQPDELVLDIIKGIPFADFELSGTKVPVSKVRLLPPVLPNKVVAFGRNYAEHARELGNEVPDAPFAFFKPSTSVIGPGDEIQYPSFSQELHHEAELAVVIGRMCREVPRERVEDVILGYTCAIDVTARDVQKREKQWARAKGFDTSCPLGPWVETDLDLATASDLTIQLTVNGQQRQLGRTSEMIHSIADLIVNISEAMTLLPGDVILTGTPAGVGPLNVGDEVAVTIEGIGTLTNKVVKRG
>NZ_LN831790.1|WP_078648180.1|2593142_2593331_-|hypothetical-protein
MKTTMMFHKIANPRRTTLAHLKDADELQTPERPEHRVELPAQTANPKRTVLNEIPVSVAAAE
>NZ_LN831790.1|WP_047121715.1|2593934_2597666_+|sensor-histidine-kinase
MQGRFKRDGSASAEPEPHGGTGPMAVSSSPQHAQNQGKHAAGDGGERPGRPGAPAPSGQTGPAAAAKQPKGPVGPGSRMALRNWRISTRLVSLLALPVVAATSLGAMRISQSLDDMQQLDNMKLLTDMTKQATELAAALQEERDQSAGPLAHGSKASAISIKGDREKTDRALKNFLESSEEIDSASKNGTLHGVRDSLVGLASDLNDLNKIRSTAYESRENSTRTVDAYHRLISHLLDLSQDMAEATSNPEMIQRTRALAAFSTAKEYASVQRAVIAAALPATNTKAGDLSENDRLYAEAALQSQRSELRSFTSIYGDGAEELLKPIDQGNPTIEATDKYAGRVLGTDGAIEEIERRSYQDWLDDSSTKIQQMKNIEHTLLEDMEQKARELRSESEREAIISGALILLVLGVSLVGAFVMARSMIRSLRRLEDTATRVAQDRLPELVKQLSESDPQDVDTSVESVGLHSRDEIGRVAAAFDDVHREAVRLAAEQALLRGNVNAMFTNLSRRSQGLIQRQLSLISELESREADPDQLSSLFKLDHLATRMRRNGENLLVLAGEEPGRRWTRPVPLVDVLRAAASEVEQYERIELSSVPTTEVAGRVVNDLVHLLAELLENATSFSSPQTKVKVTGHALPDGRVLIEIHDTGIGLSPEDLAAINERLASPPTVDVSVSRRMGLFVVGRLSQRHGIRIQLRPSDSGGTTALVMLPVDVAQGGKKPQPKQGQGPGISGGPAAAQAAAGAAAARRAAAGQGGGRGIGGPGAGGPGGGALGAGAPGGGRHGAGPGARAALPPRDGGRPGQPGAPRGPQGPGGPQEGRPAPGGPGAGQAPGAPQGLQAAGMNAPQRPDAFGGRGPAGLEQTRPGATPPRRRGRGEDQAERGRRPQLPARGGPRPELPGGDSQPRVPSWGDDNARPPVPRASLDTPRGHEEPDVSATSRMPRVDDRQGPGATAEIPAFPGTGDRHGPGATAEFARPDFGAPDPGAAGPQQTGAFPPPEAPADRFAGDAQNTEQFVRGDVFGTPAGQNDPASADRFAAPQAYDNGSTGRHALPEQPGPAAGRLERPHSDGPSAGSGFGTPQARPVRPEPEALPPAPNAGDGRTPLYDTLETNWFRGEQRQQESGPAASEPQQPQAPAASPEQPSASTAWRSPNDELVRQAERVRQPAAGGVTTSGLPRRVPRANLVPGTAQQQPHQSGPQVSRAPDDVRGRLTNLRRGIAQGRQAGAAQTGSHPRPTHQQER

Crispr_ID: NZ_LN831790_5

• CRISPR_ID: NZ_LN831790_5
• CRISPR_location: 4134903-4135016
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_LN831790_5

Consensus_repeat	Method
GGGGGCGGCGGAGGCGGGGGCGGC	CRISPRCasFinder

spacers of NZ_LN831790_5

>5.1|4134927|15|NZ_LN831790|CRISPRCasFinder
GGAGGCGGGGGCGGC
>5.2|4134966|27|NZ_LN831790|CRISPRCasFinder
GGGGGCGGCGAAGGGGGCGGCGGAGGC

CRISPR arrays and Neighbor proteins around NZ_LN831790_5

CRISPR arrays

The CRISPR arrays of NZ_LN831790_5

>merge|NZ_LN831790|5|4134903-4135016|CRISPRCasFinder
AGGCGCGCCCAGGGCGGGGGCGGCGGAGGCGGGGGCGGCGAAGGGGGCGGCGGAGGCGGAGGCGGGGGCGGCGAAGGGGGCGGCGGAGGCGGGGGCGGCACGGACGCGGGCGCC

>NZ_LN831790|5|5|4134903-4135016|CRISPRCasFinder
AGGCGCGCCCAGGGCGGGGGCGGC	GGAGGCGGGGGCGGC
GAAGGGGGCGGCGGAGGCGGAGGC	GGGGGCGGCGAAGGGGGCGGCGGAGGC
GGGGGCGGCACGGACGCGGGCGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|369272
NZ_LN831790.1|WP_047122552.1|4131506_4131695_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383910.1|4125484_4125769_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein	unknown	unknown	gnl|CDD|235933
NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein	unknown	unknown	gnl|CDD|253386
NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase	unknown	unknown	gnl|CDD|237012
NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|131480
NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase	unknown	unknown	gnl|CDD|237050
NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|197318
NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|378410
NZ_LN831790.1|WP_029383048.1|4138753_4139224_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_099053802.1|4139360_4140302_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270453
NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl|CDD|237030
NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|198080
NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase	unknown	unknown	gnl|CDD|239117
NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_LN831790.1|WP_029383050.1|4136242_4137304_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	7.09794e-37
NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|197318	cd09084, EEP-2, Exonuclease-Endonuclease-Phosphatase (EEP) domain superfamily; uncharacterized family 2. This family of uncharacterized proteins belongs to a superfamily that includes the catalytic domain (exonuclease/endonuclease/phosphatase, EEP, domain) of a diverse set of proteins including the ExoIII family of apurinic/apyrimidinic (AP) endonucleases, inositol polyphosphate 5-phosphatases (INPP5), neutral sphingomyelinases (nSMases), deadenylases (such as the vertebrate circadian-clock regulated nocturnin), bacterial cytolethal distending toxin B (CdtB), deoxyribonuclease 1 (DNase1), the endonuclease domain of the non-LTR retrotransposon LINE-1, and related domains. These diverse enzymes share a common catalytic mechanism of cleaving phosphodiester bonds; their substrates range from nucleic acids to phospholipids and perhaps, proteins.	4.13529e-26
NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein	gnl|CDD|235933	PRK07097, PRK07097, gluconate 5-dehydrogenase; Provisional.	0.00397233
NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase	gnl|CDD|237012	PRK11893, PRK11893, methionyl-tRNA synthetase; Reviewed.	0
NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase	gnl|CDD|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	4.65186e-45
NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase	gnl|CDD|237050	PRK12305, thrS, threonyl-tRNA synthetase; Reviewed.	8.93071e-177
NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.91446e-05
NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein	gnl|CDD|378410	pfam10138, vWA-TerF-like, vWA found in TerF C-terminus. vWA domain fused to TerD domain typified by the TerF protein. Some times found as solos.	6.71592e-44
NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein	gnl|CDD|253386	pfam05787, DUF839, Bacterial protein of unknown function (DUF839). This family consists of several bacterial proteins of unknown function that contain a predicted beta-propeller repeats.	0
NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein	gnl|CDD|270453	cd14750, PBP2_TMBP, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose; possesses type 2 periplasmic binding fold. This group represents the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. 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.	2.35923e-57
NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.3462e-07
NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	1.56485e-49
NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein	gnl|CDD|198080	smart01012, ANTAR, ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	1.09132e-09
NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase	gnl|CDD|239117	cd02651, nuc_hydro_IU_UC_XIUA, nuc_hydro_IU_UC_XIUA: inosine-uridine preferring, xanthosine-inosine-uridine-adenosine-preferring and, uridine-cytidine preferring nucleoside hydrolases. Nucleoside hydrolases cleave the N-glycosidic bond in nucleosides generating ribose and the respective base. These enzymes vary in their substrate specificity. This group contains proteins similar to nucleoside hydrolases which hydrolyze both pyrimidine and purine ribonucleosides: the inosine-uridine preferring nucleoside hydrolase from Crithidia fasciculata, the inosine-uridine-xanthosine preferring nucleoside hydrolase RihC from Escherichia coli and the xanthosine-inosine-uridine-adenosine-preferring nucleoside hydrolase RihC from Salmonella enterica serovar Typhimurium. This group also contains proteins similar to the pyrimidine-specific uridine-cytidine preferring nucleoside hydrolases URH1 from Saccharomyces cerevisiae, E. coli RihA and E. coli RihB. E. coli RihA is equally efficient with uridine and cytidine, E. coli RihB prefers cytidine over uridine. S. cerevisiae URH1 prefers uridine over cytidine. .	3.75353e-117
NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.32993e-15

Protein sequences

>NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein
MTRSPAGRTAVPRLLAALLAALLGLAACTGGGDDRGRGGAQAPPTAEGPGDIVIASGRDVTGRNGVRQRLIDAWNTRQERRGTGYRARLVELPGSADEQRSQLLGALQSGSAGYDVVNLDVTWVPEFAAAGLIRPLPEGMVDDDVIASVASTARWDGRVYAVPFNSDVGLLYYRRDYLERAGVQHTDLGSGLDWDRLRTLIIALDDRKPGAYDQGWTTQLAAYEGRTVNALEAFASAVPDLTLTDGDGRYRATVEELARGIAELRKRSEASYILPGAFRSDEAASAGDFADGRTAFLRHWPYVYRTLYQSFTEEQLAVAPLPGRAVLGGQNLAVTDASRRAGKATELIAFLTGRESERCLLDAGFAATRASAYTDDGVRCTVAAPRGPSPSSTGESADRMPRDAAGRPEYARRILLPALHRAVHRPRTPLYGAFTQAFTARLGTLFGPRPPSDQDLARALDADLRKALPD
>NZ_LN831790.1|WP_047122552.1|4131506_4131695_+|hypothetical-protein
MLVRTPSAERYVRGFAAAAVAMAALVLAANAGPVQPTGSAPADPRTAHTPGASVTEAEAQRP
>NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein
MGRAKPGEVPGRLCEVAVRLLPVTGASASLRSDGVPVQLCASGDLAAYLSDIQTTLGEGPCVEATETGRPVLARDLATGPDARRWPVYAQEATAVGVRAVYALPLGNDSVCVGTLDLYRDTPGTLTGPELHTARLIAAVMTVALMALPHGEEYDSQGGAPWLSGLAAEHDEVFQAVGMIMAQLGVGADEALARLRAHAFAHGRTAHDVARAVVTHRERFERDR
>NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein
MSFVIDRYPCEESPRLGAMTLRPTPDSVPRARRWFRRFIAPYDPRCSVDDCVLALSELVTNAVLHGRADAEWVLRVEWFRDGTSLRVEVHNPGLPEGVCLRRPDADDLHGRGLLLVDSVAASWDCGPSRFGGTVVSFVMADAWPP
>NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator
MATTDDRRPKYQRIADSLREAIETGEYGPGDRLPGENELMSTYGVARMTARQALSVLREEGVAEARKGAGVFVRAFRPLRRRGIHRLSRDQWGDGRSIWSADIENRDLEVDGITVSEEPAPEHIGAVLDLADGEAVCVRRRRFVLDGKPVLLATSHLPMSLVAGSAITREDTGPGGTYARLAELGHAPVHFREEIRSRMPSKDETTRLSMSAGTPVILICRTAYTAEGRPVEVNEMTLDASSYILEYDFDAGPGTATADN
>NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase
MPAAQRTSVAASVSVRPLVEPDLDRADEIFRVAFGTFLGAPEPKTFFGTADYVRTRWAADPDAAFAATVEGKVVGSNFAADWGSVGYFGPLTVRPDLWDQGVGRRLMEPVMACFDTWENRHLGLFTFSHSPKHLELYRRYGFWPRFLTAIMKKQVTTGAAVPGRVLYGGLTAAERPQALSLSRALTGAVYEGLSLEREIMAVQAQGLGDTILLTGADSGLDGLAVCHCGAGSEAGEDVCFVKFGAVRPGPDAADRFERLLDACEHLATEKGLGQLDAGMNLARQDAYRRMVDRGFRTWLQGVTMHKPNEPGYSHPDAYVIDDWR
>NZ_LN831790.1|WP_029383910.1|4125484_4125769_-|hypothetical-protein
MKLRNAVACTFAAFAVVGGATGAAQAAAGDDRARFDNGEQVASCDIVEIGDQPNLGPSENNVDCSRNITEREAESVYIVGGPVASLLPLRPAQG
>NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase
MHDHRHLGRDLGVFGTDPLMGAGLPYWLPDGATVRHTLEEYVREAELRAGYRHVHSPDLGKRELYEISGHWDLYREDMFPPMRLGAEEVVLRPSLCPHHALVYRSRGRSHRELPLRIAELGTMYRSEPSGVLGGLTRVRAIHLNDAHIFCTPEQAAGEARAALGLIRRAYADLGIRAARYRLSLPGPGGKYVADPELWRRATALLEEALDGQPYEAAEGEAAFYGPKIDVQIADAAGRETTLSTVQIDFHQPARFGLRYTGADGRGHRPVMVHRSVIGSVERAVAHLIEVSGGAFPVWLAPVQLVVLPVGEAQEERAYELVGEAVSRGVRAEVAGPARGTLGARIRAARLVPYQAVIGEREAAGGDLGAVRLRDGRRPGAVSGAELLRRIGERARERGWELWGDA
>NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase
MAVTTEQPIPVIIDCDTGIDDALALLFAVRHPGLDLRAVTCVAGNTDVDGVVRNTLTVLEQAGAPAVPVARGAERPLIEAVRTARHVHGRDGMGDLGLPAPTRTAVDVDAVTLLRREILASPRPVTLVPTAPLTNIALLLRTHPEVTRNIERIVFMGGAVATGNATPVAEFNVWHDPEAAAVLLTAGVPMTMYGLDVFQQVVVPGADVTRLRGSTEPGARLAGELLAHRGPATDETEPGGGLGDAGAVCAVADPAGLTTELLPVEVALAPGPTRGQTIVDRRARPGESEIHEGGREQTLVDVALGVDVERYVKLYLAAVEGP
>NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein
MSIARRVTVRRLLGAGAASLALCAASVASASGAFAHGAPGGHGWGSGGGYKPGTGAGTVTETDRCQFSLDGTAFSDSVKVDDQNLKPTEDGKVHIKVRTAGSATTCTASLASYLAHGATFATSGEQVFVDFDTVTVKPGETGSLDIAVPDAGCYAQIDLYRGAVRYDGELEANDGFEHGPLPKGPDGTVIKDKLIAAWNGGTKDCTADTPEPPAEPEPSAPEPSAPSDTPEPSAPATESPAGTPSADTPSSRPPASESPASQAPSASASAPAAAAPSATPNGGSGDLAETGAGSSTLPLAIGAAVLLAGGAGIVVATRRRRTARS
>NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein
MAEGDGVTTRGIRIRLDGTATESDIGALHKWLEREKPLEELVRTGRLRIHERSRTDETGAPMGIGMEIVVALAGAAGSVLFQELLDQVKKAVQAWRDNRREVEDGEPPEGRVEPVNLDDR
>NZ_LN831790.1|WP_029383050.1|4136242_4137304_-|hypothetical-protein
MPGTVLLLAASPVGKGRLVDAASVLPVLAAVPPSVLSGADTASVIELADPLEPQAVLTRLRAAAAAPGPLTVYVTGQLQLDRRQRLPHLALARTTPATVRYTALPWQWIREELRLRPPGATTLLLDLHADQEMWEWLGAHPLDSGRNNAVYGRIAPPPARRAVAAPVYMKSLATILRSGHRPPLDQLHQLALARTAAEGPPPGLVLTAPGPVPSDPHAAIAAAVQAGRHADADALAAHHERAARQAYGTASEEALHWAEVRADLAMLAGDPVRSCRTWLTVATARLNAGQAPDAPAVEAAADRAHHQWGRIRDPARARELGGALAELRARVPGRRAGALDHVRRELSRLQTQV
>NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase
MRAGRHRVSLGRVRGGDVPRPTGGRWWPPGPPSRARGGAEAAYRNQPLMRLRGRSMGWVPPLLLLAGIAVADFNTTGEFRIISWIVLVPGIAAALCGVWGTAVFAVLALLTYVTVDSAWPHQYQTGLPDFILVTVGSILAVAACVVRVRGERRMLHMRDIADTTRRTVLRPLPPGWGGLEHAGVYLASDTEARVGGDFYDIQPGPHGTRVLVGDVQGKGLGAVEAAAALLGTFREAGYHEADLATVAERLETRIVRHRNHTAALGRKADGDRFATAVLLGFPEDAPGAVDAVVFGHEPPLAVGPGGVRQLPAGDGLPLGLGELAPARPTVRRLPLAPDETLLLVTDGVTEARDRQGCFYRLRDEVARAVAADPGVTEPRRLAAHVRDGTLRHCGGRLDDDTTVFAVRRPPHPRDE
>NZ_LN831790.1|WP_029383048.1|4138753_4139224_+|hypothetical-protein
MTYAAPASGGTSGRALPSGRPPARTPDVFGPGVHAAAKWAVPVVLGLVYGYWAAANRRGGGPVTGWNLLFGFLTALAFMVLYAVVRTVARRLGRTPHAALWAAFTGSAVGFLYRQSESATLLRSCGIGLAVGLPLFLMLFYRYYTREEVEERPPTA
>NZ_LN831790.1|WP_099053802.1|4139360_4140302_+|hypothetical-protein
MVPRNVPRNVPRNVLSAVLTALACLLVPCATLAGWVAYGLADTGRYTAAMAPLADDPRVREAVADAVGDGLAREAGTGPLRGAMGPYLQDAARSFTRTDAFRAGWDTANRTVHAAVLRALRAERPQHRPVTVDLARVTVRVKEELVRDHVPFAHRIPVRHTEITVLPAARTDRLRKGYHMLDIAARWLPCAAVAFALAGIATATRRRRAITATGLGTALGGALLLLAVAAGRRLTLTALPGPPGRPAAGAVYDALTTTLRTASWLLVALGLTVALASCLTGLLPRHRAPVPAGTPDPAVAAEPRPSSSTPLPP
>NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase
MAPFLAYEDRGGSGDPAATPLVLVHGHPFDRTMWTPQTEVFAASRRVIAPDLRGYGASPVTPALTDFGGFARDIEALLDELEVASCVLAGVSMGGQIAMECYGRFPHRVRGLVLADTSPAAETPEGRTARRAMADRLLREGLRGYADEVLEKMVAPYADPQVKAHVHRMMTATRPEGAAAALRARAERPDYRELLSRATVPALVVVGADDTYTPVPGAEALHALLPDASLCVVEGAAHLPNLERPERFNAALEEFLARVDARV
>NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein
MREGRAAVTPRWAVVDPPGGRRRRRGAGCAGLLLAAVSVVAGCRAAGSDGITPVPQLLAFLPWLLVPAGAGLLLALFARWWTGAVWGVLLLGLLAWHIEPYGTTGDPIGLPVAEVRVLTSNVEFGQGTGALIEAVRREKPDLVFVQECPSLCDAALRGRLAEDYPHRRAVEGEGPRGSVILSRFPLRATAGIPATMGMPAAVADVRGHSVRLQLAHPMPPLPGQVDRWRAELDAVRDAAAADTRTPTVLAGDFNAGQDHAAFRRILDTGLRDAARLAGSPRAPTWPSPTTPGFGTQIDHVLVSEDFTVHDARFLGIAGSDHRAVVVGLTLHGRG
>NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein
MRKLLPLIGTPSGSHPGGRSAMTCRFRCGDACFHEVPNTSSNEYVGDVIAGALSRRSMMRAAAVVTVAAAGAGTVTLAGAPEANAAPAAQAAARGKQKGARGLRFTPVAPNTRDAVVVPEGYRQNVVIRWGEPILRGAPAFDPDHQSAEAQAGQFGYNNDFLALLPLPGERNRQLLVANHEYTDEVLMFRGYDPDNPTREQVEIAWAAHGLSAVVVEEDRRTGKLTPVTRHHLNRRVTATTEFRLTGPAAGSELVKTSADRTGTKVLGTLNNCSGGTTPWGTTLHGEENFNQYFANSSRATDKRYGIGTGATERKWERFDKRFDVAQEPNEVHRFGYVVEFDPYDPHSTPRKHTALGRFKHEAATVRLTHDGRPVVYSGDDERFDYFYKFVGSKRMKKGTSRAVREHNLSLLDEGTLYVAKLTGDSPAIEIDGTGKLPGDGEFDGSGQWIPLVTATADGAVSHVPGMTAEEVCVFTRLAGDKVGATKMDRPEDIEPSPVTGKVYVALTNNSNRGKAGYTGPDEANPRNSNKHGHVLELTERWNRPESTAFAWSLFLVAGDPEDPATYFAGFPKDAVSPISCPDNVAFDPHGNLWLSTDGNALGSHDGLFGVAVKGDRRGELKQFLTVPTGAETCGPVVQDRRVLVAVQHPGEVDGASVDKPASTWPDGPGSLVRPAVVAVWRADGGDIGV
>NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein
MGILTLLRNAFGRSRKAKTAQAEDAAPQPPAQTAPEPAPATAPETAPDAAPPTAAEAPPAPEPKLPSQSAPRTTTAAPAPAPQVPEPRPSGPGEHELVTAAFDKVTVPRPTRTPEQEDTPTTIEAEPEPRGEAKPEAEPEPRGEAKPEAEPEPRGEAKPEAESESDTKTESETRTESDTRTESDTKTETRSEAELEPEPKAETESEPETEAHREPETETAPKPEAGTDTETGPEIGTGPATGTVTEAEAETETETGTGTGTGTGTGTQAEAQTDTEPEPGTDTDTDTRAQAETQPKPETDTEARPETQPQPETETDTEAEAGTDTGAEQAPREPQPQPAPSPKPASAPEPEPATKGPAETEPATADEVKSGKPAVSAARVRSRAPHLSTAYKAAGAALRKYGLTGARAKVYLVLDRSASMRPYYKDGSAQALAEQTLALAAHLDPEATVPVVFFSTELDGTGELTLDEHENKIDELHAALGRMGRTSYHAAVEEVLAAHGKSAPGTPALVVFQTDGAPDAKTPATRSLEEAAADRPAVFFSFVAFGDPENKAFDYLRKLRTGNASHFLAGEAPRELTDKELYEGILASWRP
>NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase
MAATGSEKQGGKAFYVSTPIYYVNDAPHLGHAYTTVAGDVLTRWHRQRGEKVWYLTGTDEHGQKIMRTAEANGVSPQEWADKLVTEAWKPLWEHLEIANDDFIRTTQQRHTDRVQEFVQDLYDKGEIYKGGYEGPYCVGCEEYKLPGELLDGEGEYAGQKLCPIHKKPVETLSEENYFFKLSEYGDRLLAHYEANPDFIQPESARNEVVNFVRQGLQDLSISRSTFDWGIPIPWDEKHVIYVWVDALLNYATAVGYNENQEKFEATFPADVHLVGKDILRFHAVIWPAMLMAQGLPLPGKIAANGWLMVGGEKMSKSNLTGIKPQDLTSHFGVDAYRWYFLRAIAFGQDGSFSWEDFSARYTSELANDYGNLASRVAAMVGKYFGGTLPEATAVGEAEKAIHAHLAKAVTEADRKIGEKLDFQGGILAVFDFIKQVNGYITEQEPWKVAKDDSPEGKARLATILYTAAESLRAVAVLLNPVMPQTSQKLWDSLGADASLGRLADQKVQEAGDWGRLPAGSTVTKGAVLFPRLEEKPSA

Crispr_ID: NZ_LN831790_4

• CRISPR_ID: NZ_LN831790_4
• CRISPR_location: 4134653-4134818
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_LN831790_4

Consensus_repeat	Method
GGGGGCGGCGGAGGCGGGGGCGGC	CRISPRCasFinder

spacers of NZ_LN831790_4

>4.1|4134677|51|NZ_LN831790|CRISPRCasFinder
GGGCTCCAGATCGGGGTCGGTCAGCACGCGCAGCTCCAGAGCCGGTCCGCA
>4.2|4134752|42|NZ_LN831790|CRISPRCasFinder
GGTGACCACGTACCAGCCGAGGCCGAAGGCGGTCAGGCCGAG

CRISPR arrays and Neighbor proteins around NZ_LN831790_4

CRISPR arrays

The CRISPR arrays of NZ_LN831790_4

>merge|NZ_LN831790|4|4134653-4134818|CRISPRCasFinder
GGCGTCGGCGGCGGCCCGGACGGTGGGCTCCAGATCGGGGTCGGTCAGCACGCGCAGCTCCAGAGCCGGTCCGCAGGGGGCGTCGTCGGCGACGACGGCGGTGACCACGTACCAGCCGAGGCCGAAGGCGGTCAGGCCGAGCAGGACGACGGCGGCGCGGGCGGCC

>NZ_LN831790|4|4|4134653-4134818|CRISPRCasFinder
GGCGTCGGCGGCGGCCCGGACGGT	GGGCTCCAGATCGGGGTCGGTCAGCACGCGCAGCTCCAGAGCCGGTCCGCA
GGGGGCGTCGTCGGCGACGACGGC	GGTGACCACGTACCAGCCGAGGCCGAAGGCGGTCAGGCCGAG
CAGGACGACGGCGGCGCGGGCGGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|369272
NZ_LN831790.1|WP_047122552.1|4131506_4131695_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383910.1|4125484_4125769_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein	unknown	unknown	gnl|CDD|235933
NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein	unknown	unknown	gnl|CDD|253386
NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase	unknown	unknown	gnl|CDD|237012
NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|131480
NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase	unknown	unknown	gnl|CDD|237050
NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|197318
NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|378410
NZ_LN831790.1|WP_029383048.1|4138753_4139224_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_099053802.1|4139360_4140302_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270453
NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl|CDD|237030
NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|198080
NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase	unknown	unknown	gnl|CDD|239117
NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_LN831790.1|WP_029383050.1|4136242_4137304_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	7.09794e-37
NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|197318	cd09084, EEP-2, Exonuclease-Endonuclease-Phosphatase (EEP) domain superfamily; uncharacterized family 2. This family of uncharacterized proteins belongs to a superfamily that includes the catalytic domain (exonuclease/endonuclease/phosphatase, EEP, domain) of a diverse set of proteins including the ExoIII family of apurinic/apyrimidinic (AP) endonucleases, inositol polyphosphate 5-phosphatases (INPP5), neutral sphingomyelinases (nSMases), deadenylases (such as the vertebrate circadian-clock regulated nocturnin), bacterial cytolethal distending toxin B (CdtB), deoxyribonuclease 1 (DNase1), the endonuclease domain of the non-LTR retrotransposon LINE-1, and related domains. These diverse enzymes share a common catalytic mechanism of cleaving phosphodiester bonds; their substrates range from nucleic acids to phospholipids and perhaps, proteins.	4.13529e-26
NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein	gnl|CDD|235933	PRK07097, PRK07097, gluconate 5-dehydrogenase; Provisional.	0.00397233
NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase	gnl|CDD|237012	PRK11893, PRK11893, methionyl-tRNA synthetase; Reviewed.	0
NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase	gnl|CDD|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	4.65186e-45
NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase	gnl|CDD|237050	PRK12305, thrS, threonyl-tRNA synthetase; Reviewed.	8.93071e-177
NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.91446e-05
NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein	gnl|CDD|378410	pfam10138, vWA-TerF-like, vWA found in TerF C-terminus. vWA domain fused to TerD domain typified by the TerF protein. Some times found as solos.	6.71592e-44
NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein	gnl|CDD|253386	pfam05787, DUF839, Bacterial protein of unknown function (DUF839). This family consists of several bacterial proteins of unknown function that contain a predicted beta-propeller repeats.	0
NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein	gnl|CDD|270453	cd14750, PBP2_TMBP, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose; possesses type 2 periplasmic binding fold. This group represents the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. 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.	2.35923e-57
NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.3462e-07
NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	1.56485e-49
NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein	gnl|CDD|198080	smart01012, ANTAR, ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	1.09132e-09
NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase	gnl|CDD|239117	cd02651, nuc_hydro_IU_UC_XIUA, nuc_hydro_IU_UC_XIUA: inosine-uridine preferring, xanthosine-inosine-uridine-adenosine-preferring and, uridine-cytidine preferring nucleoside hydrolases. Nucleoside hydrolases cleave the N-glycosidic bond in nucleosides generating ribose and the respective base. These enzymes vary in their substrate specificity. This group contains proteins similar to nucleoside hydrolases which hydrolyze both pyrimidine and purine ribonucleosides: the inosine-uridine preferring nucleoside hydrolase from Crithidia fasciculata, the inosine-uridine-xanthosine preferring nucleoside hydrolase RihC from Escherichia coli and the xanthosine-inosine-uridine-adenosine-preferring nucleoside hydrolase RihC from Salmonella enterica serovar Typhimurium. This group also contains proteins similar to the pyrimidine-specific uridine-cytidine preferring nucleoside hydrolases URH1 from Saccharomyces cerevisiae, E. coli RihA and E. coli RihB. E. coli RihA is equally efficient with uridine and cytidine, E. coli RihB prefers cytidine over uridine. S. cerevisiae URH1 prefers uridine over cytidine. .	3.75353e-117
NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.32993e-15

Protein sequences

>NZ_LN831790.1|WP_029383901.1|4131716_4133129_-|extracellular-solute-binding-protein
MTRSPAGRTAVPRLLAALLAALLGLAACTGGGDDRGRGGAQAPPTAEGPGDIVIASGRDVTGRNGVRQRLIDAWNTRQERRGTGYRARLVELPGSADEQRSQLLGALQSGSAGYDVVNLDVTWVPEFAAAGLIRPLPEGMVDDDVIASVASTARWDGRVYAVPFNSDVGLLYYRRDYLERAGVQHTDLGSGLDWDRLRTLIIALDDRKPGAYDQGWTTQLAAYEGRTVNALEAFASAVPDLTLTDGDGRYRATVEELARGIAELRKRSEASYILPGAFRSDEAASAGDFADGRTAFLRHWPYVYRTLYQSFTEEQLAVAPLPGRAVLGGQNLAVTDASRRAGKATELIAFLTGRESERCLLDAGFAATRASAYTDDGVRCTVAAPRGPSPSSTGESADRMPRDAAGRPEYARRILLPALHRAVHRPRTPLYGAFTQAFTARLGTLFGPRPPSDQDLARALDADLRKALPD
>NZ_LN831790.1|WP_047122552.1|4131506_4131695_+|hypothetical-protein
MLVRTPSAERYVRGFAAAAVAMAALVLAANAGPVQPTGSAPADPRTAHTPGASVTEAEAQRP
>NZ_LN831790.1|WP_078648222.1|4130298_4130970_-|GAF-and-ANTAR-domain-containing-protein
MGRAKPGEVPGRLCEVAVRLLPVTGASASLRSDGVPVQLCASGDLAAYLSDIQTTLGEGPCVEATETGRPVLARDLATGPDARRWPVYAQEATAVGVRAVYALPLGNDSVCVGTLDLYRDTPGTLTGPELHTARLIAAVMTVALMALPHGEEYDSQGGAPWLSGLAAEHDEVFQAVGMIMAQLGVGADEALARLRAHAFAHGRTAHDVARAVVTHRERFERDR
>NZ_LN831790.1|WP_029383904.1|4129802_4130240_+|ATP-binding-protein
MSFVIDRYPCEESPRLGAMTLRPTPDSVPRARRWFRRFIAPYDPRCSVDDCVLALSELVTNAVLHGRADAEWVLRVEWFRDGTSLRVEVHNPGLPEGVCLRRPDADDLHGRGLLLVDSVAASWDCGPSRFGGTVVSFVMADAWPP
>NZ_LN831790.1|WP_029383905.1|4128723_4129506_-|GntR-family-transcriptional-regulator
MATTDDRRPKYQRIADSLREAIETGEYGPGDRLPGENELMSTYGVARMTARQALSVLREEGVAEARKGAGVFVRAFRPLRRRGIHRLSRDQWGDGRSIWSADIENRDLEVDGITVSEEPAPEHIGAVLDLADGEAVCVRRRRFVLDGKPVLLATSHLPMSLVAGSAITREDTGPGGTYARLAELGHAPVHFREEIRSRMPSKDETTRLSMSAGTPVILICRTAYTAEGRPVEVNEMTLDASSYILEYDFDAGPGTATADN
>NZ_LN831790.1|WP_047121888.1|4126914_4127889_-|GNAT-family-N-acetyltransferase
MPAAQRTSVAASVSVRPLVEPDLDRADEIFRVAFGTFLGAPEPKTFFGTADYVRTRWAADPDAAFAATVEGKVVGSNFAADWGSVGYFGPLTVRPDLWDQGVGRRLMEPVMACFDTWENRHLGLFTFSHSPKHLELYRRYGFWPRFLTAIMKKQVTTGAAVPGRVLYGGLTAAERPQALSLSRALTGAVYEGLSLEREIMAVQAQGLGDTILLTGADSGLDGLAVCHCGAGSEAGEDVCFVKFGAVRPGPDAADRFERLLDACEHLATEKGLGQLDAGMNLARQDAYRRMVDRGFRTWLQGVTMHKPNEPGYSHPDAYVIDDWR
>NZ_LN831790.1|WP_029383910.1|4125484_4125769_-|hypothetical-protein
MKLRNAVACTFAAFAVVGGATGAAQAAAGDDRARFDNGEQVASCDIVEIGDQPNLGPSENNVDCSRNITEREAESVYIVGGPVASLLPLRPAQG
>NZ_LN831790.1|WP_029383912.1|4123955_4125173_-|threonine--tRNA-ligase
MHDHRHLGRDLGVFGTDPLMGAGLPYWLPDGATVRHTLEEYVREAELRAGYRHVHSPDLGKRELYEISGHWDLYREDMFPPMRLGAEEVVLRPSLCPHHALVYRSRGRSHRELPLRIAELGTMYRSEPSGVLGGLTRVRAIHLNDAHIFCTPEQAAGEARAALGLIRRAYADLGIRAARYRLSLPGPGGKYVADPELWRRATALLEEALDGQPYEAAEGEAAFYGPKIDVQIADAAGRETTLSTVQIDFHQPARFGLRYTGADGRGHRPVMVHRSVIGSVERAVAHLIEVSGGAFPVWLAPVQLVVLPVGEAQEERAYELVGEAVSRGVRAEVAGPARGTLGARIRAARLVPYQAVIGEREAAGGDLGAVRLRDGRRPGAVSGAELLRRIGERARERGWELWGDA
>NZ_LN831790.1|WP_099053801.1|4122931_4123900_-|nucleoside-hydrolase
MAVTTEQPIPVIIDCDTGIDDALALLFAVRHPGLDLRAVTCVAGNTDVDGVVRNTLTVLEQAGAPAVPVARGAERPLIEAVRTARHVHGRDGMGDLGLPAPTRTAVDVDAVTLLRREILASPRPVTLVPTAPLTNIALLLRTHPEVTRNIERIVFMGGAVATGNATPVAEFNVWHDPEAAAVLLTAGVPMTMYGLDVFQQVVVPGADVTRLRGSTEPGARLAGELLAHRGPATDETEPGGGLGDAGAVCAVADPAGLTTELLPVEVALAPGPTRGQTIVDRRARPGESEIHEGGREQTLVDVALGVDVERYVKLYLAAVEGP
>NZ_LN831790.1|WP_029383915.1|4121856_4122834_+|LPXTG-cell-wall-anchor-domain-containing-protein
MSIARRVTVRRLLGAGAASLALCAASVASASGAFAHGAPGGHGWGSGGGYKPGTGAGTVTETDRCQFSLDGTAFSDSVKVDDQNLKPTEDGKVHIKVRTAGSATTCTASLASYLAHGATFATSGEQVFVDFDTVTVKPGETGSLDIAVPDAGCYAQIDLYRGAVRYDGELEANDGFEHGPLPKGPDGTVIKDKLIAAWNGGTKDCTADTPEPPAEPEPSAPEPSAPSDTPEPSAPATESPAGTPSADTPSSRPPASESPASQAPSASASAPAAAAPSATPNGGSGDLAETGAGSSTLPLAIGAAVLLAGGAGIVVATRRRRTARS
>NZ_LN831790.1|WP_029383051.1|4135757_4136120_-|hypothetical-protein
MAEGDGVTTRGIRIRLDGTATESDIGALHKWLEREKPLEELVRTGRLRIHERSRTDETGAPMGIGMEIVVALAGAAGSVLFQELLDQVKKAVQAWRDNRREVEDGEPPEGRVEPVNLDDR
>NZ_LN831790.1|WP_029383050.1|4136242_4137304_-|hypothetical-protein
MPGTVLLLAASPVGKGRLVDAASVLPVLAAVPPSVLSGADTASVIELADPLEPQAVLTRLRAAAAAPGPLTVYVTGQLQLDRRQRLPHLALARTTPATVRYTALPWQWIREELRLRPPGATTLLLDLHADQEMWEWLGAHPLDSGRNNAVYGRIAPPPARRAVAAPVYMKSLATILRSGHRPPLDQLHQLALARTAAEGPPPGLVLTAPGPVPSDPHAAIAAAVQAGRHADADALAAHHERAARQAYGTASEEALHWAEVRADLAMLAGDPVRSCRTWLTVATARLNAGQAPDAPAVEAAADRAHHQWGRIRDPARARELGGALAELRARVPGRRAGALDHVRRELSRLQTQV
>NZ_LN831790.1|WP_029383049.1|4137389_4138637_-|serine/threonine-protein-phosphatase
MRAGRHRVSLGRVRGGDVPRPTGGRWWPPGPPSRARGGAEAAYRNQPLMRLRGRSMGWVPPLLLLAGIAVADFNTTGEFRIISWIVLVPGIAAALCGVWGTAVFAVLALLTYVTVDSAWPHQYQTGLPDFILVTVGSILAVAACVVRVRGERRMLHMRDIADTTRRTVLRPLPPGWGGLEHAGVYLASDTEARVGGDFYDIQPGPHGTRVLVGDVQGKGLGAVEAAAALLGTFREAGYHEADLATVAERLETRIVRHRNHTAALGRKADGDRFATAVLLGFPEDAPGAVDAVVFGHEPPLAVGPGGVRQLPAGDGLPLGLGELAPARPTVRRLPLAPDETLLLVTDGVTEARDRQGCFYRLRDEVARAVAADPGVTEPRRLAAHVRDGTLRHCGGRLDDDTTVFAVRRPPHPRDE
>NZ_LN831790.1|WP_029383048.1|4138753_4139224_+|hypothetical-protein
MTYAAPASGGTSGRALPSGRPPARTPDVFGPGVHAAAKWAVPVVLGLVYGYWAAANRRGGGPVTGWNLLFGFLTALAFMVLYAVVRTVARRLGRTPHAALWAAFTGSAVGFLYRQSESATLLRSCGIGLAVGLPLFLMLFYRYYTREEVEERPPTA
>NZ_LN831790.1|WP_099053802.1|4139360_4140302_+|hypothetical-protein
MVPRNVPRNVPRNVLSAVLTALACLLVPCATLAGWVAYGLADTGRYTAAMAPLADDPRVREAVADAVGDGLAREAGTGPLRGAMGPYLQDAARSFTRTDAFRAGWDTANRTVHAAVLRALRAERPQHRPVTVDLARVTVRVKEELVRDHVPFAHRIPVRHTEITVLPAARTDRLRKGYHMLDIAARWLPCAAVAFALAGIATATRRRRAITATGLGTALGGALLLLAVAAGRRLTLTALPGPPGRPAAGAVYDALTTTLRTASWLLVALGLTVALASCLTGLLPRHRAPVPAGTPDPAVAAEPRPSSSTPLPP
>NZ_LN831790.1|WP_029383046.1|4140327_4141119_+|alpha/beta-fold-hydrolase
MAPFLAYEDRGGSGDPAATPLVLVHGHPFDRTMWTPQTEVFAASRRVIAPDLRGYGASPVTPALTDFGGFARDIEALLDELEVASCVLAGVSMGGQIAMECYGRFPHRVRGLVLADTSPAAETPEGRTARRAMADRLLREGLRGYADEVLEKMVAPYADPQVKAHVHRMMTATRPEGAAAALRARAERPDYRELLSRATVPALVVVGADDTYTPVPGAEALHALLPDASLCVVEGAAHLPNLERPERFNAALEEFLARVDARV
>NZ_LN831790.1|WP_047121890.1|4141175_4142180_+|endonuclease/exonuclease/phosphatase-family-protein
MREGRAAVTPRWAVVDPPGGRRRRRGAGCAGLLLAAVSVVAGCRAAGSDGITPVPQLLAFLPWLLVPAGAGLLLALFARWWTGAVWGVLLLGLLAWHIEPYGTTGDPIGLPVAEVRVLTSNVEFGQGTGALIEAVRREKPDLVFVQECPSLCDAALRGRLAEDYPHRRAVEGEGPRGSVILSRFPLRATAGIPATMGMPAAVADVRGHSVRLQLAHPMPPLPGQVDRWRAELDAVRDAAAADTRTPTVLAGDFNAGQDHAAFRRILDTGLRDAARLAGSPRAPTWPSPTTPGFGTQIDHVLVSEDFTVHDARFLGIAGSDHRAVVVGLTLHGRG
>NZ_LN831790.1|WP_029383044.1|4142324_4144397_-|PhoX-family-protein
MRKLLPLIGTPSGSHPGGRSAMTCRFRCGDACFHEVPNTSSNEYVGDVIAGALSRRSMMRAAAVVTVAAAGAGTVTLAGAPEANAAPAAQAAARGKQKGARGLRFTPVAPNTRDAVVVPEGYRQNVVIRWGEPILRGAPAFDPDHQSAEAQAGQFGYNNDFLALLPLPGERNRQLLVANHEYTDEVLMFRGYDPDNPTREQVEIAWAAHGLSAVVVEEDRRTGKLTPVTRHHLNRRVTATTEFRLTGPAAGSELVKTSADRTGTKVLGTLNNCSGGTTPWGTTLHGEENFNQYFANSSRATDKRYGIGTGATERKWERFDKRFDVAQEPNEVHRFGYVVEFDPYDPHSTPRKHTALGRFKHEAATVRLTHDGRPVVYSGDDERFDYFYKFVGSKRMKKGTSRAVREHNLSLLDEGTLYVAKLTGDSPAIEIDGTGKLPGDGEFDGSGQWIPLVTATADGAVSHVPGMTAEEVCVFTRLAGDKVGATKMDRPEDIEPSPVTGKVYVALTNNSNRGKAGYTGPDEANPRNSNKHGHVLELTERWNRPESTAFAWSLFLVAGDPEDPATYFAGFPKDAVSPISCPDNVAFDPHGNLWLSTDGNALGSHDGLFGVAVKGDRRGELKQFLTVPTGAETCGPVVQDRRVLVAVQHPGEVDGASVDKPASTWPDGPGSLVRPAVVAVWRADGGDIGV
>NZ_LN831790.1|WP_047121891.1|4144652_4146428_+|VWA-domain-containing-protein
MGILTLLRNAFGRSRKAKTAQAEDAAPQPPAQTAPEPAPATAPETAPDAAPPTAAEAPPAPEPKLPSQSAPRTTTAAPAPAPQVPEPRPSGPGEHELVTAAFDKVTVPRPTRTPEQEDTPTTIEAEPEPRGEAKPEAEPEPRGEAKPEAEPEPRGEAKPEAESESDTKTESETRTESDTRTESDTKTETRSEAELEPEPKAETESEPETEAHREPETETAPKPEAGTDTETGPEIGTGPATGTVTEAEAETETETGTGTGTGTGTGTQAEAQTDTEPEPGTDTDTDTRAQAETQPKPETDTEARPETQPQPETETDTEAEAGTDTGAEQAPREPQPQPAPSPKPASAPEPEPATKGPAETEPATADEVKSGKPAVSAARVRSRAPHLSTAYKAAGAALRKYGLTGARAKVYLVLDRSASMRPYYKDGSAQALAEQTLALAAHLDPEATVPVVFFSTELDGTGELTLDEHENKIDELHAALGRMGRTSYHAAVEEVLAAHGKSAPGTPALVVFQTDGAPDAKTPATRSLEEAAADRPAVFFSFVAFGDPENKAFDYLRKLRTGNASHFLAGEAPRELTDKELYEGILASWRP
>NZ_LN831790.1|WP_029383383.1|4146523_4148140_+|methionine--tRNA-ligase
MAATGSEKQGGKAFYVSTPIYYVNDAPHLGHAYTTVAGDVLTRWHRQRGEKVWYLTGTDEHGQKIMRTAEANGVSPQEWADKLVTEAWKPLWEHLEIANDDFIRTTQQRHTDRVQEFVQDLYDKGEIYKGGYEGPYCVGCEEYKLPGELLDGEGEYAGQKLCPIHKKPVETLSEENYFFKLSEYGDRLLAHYEANPDFIQPESARNEVVNFVRQGLQDLSISRSTFDWGIPIPWDEKHVIYVWVDALLNYATAVGYNENQEKFEATFPADVHLVGKDILRFHAVIWPAMLMAQGLPLPGKIAANGWLMVGGEKMSKSNLTGIKPQDLTSHFGVDAYRWYFLRAIAFGQDGSFSWEDFSARYTSELANDYGNLASRVAAMVGKYFGGTLPEATAVGEAEKAIHAHLAKAVTEADRKIGEKLDFQGGILAVFDFIKQVNGYITEQEPWKVAKDDSPEGKARLATILYTAAESLRAVAVLLNPVMPQTSQKLWDSLGADASLGRLADQKVQEAGDWGRLPAGSTVTKGAVLFPRLEEKPSA

Crispr_ID: NZ_LN831790_6

• CRISPR_ID: NZ_LN831790_6
• CRISPR_location: 4180718-4180867
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_LN831790_6

Consensus_repeat	Method
CGGTGGCGGCGCGTGGTTCCGCGG	CRISPRCasFinder

spacers of NZ_LN831790_6

>6.1|4180742|48|NZ_LN831790|CRISPRCasFinder
CGGGACCCGGAGCGGTGGCGGCGCGTGGTTCCGCGGCGGGACCCGGAG
>6.2|4180814|30|NZ_LN831790|CRISPRCasFinder
GGGCGTACGGCCCCGAGGCGGCGTACAGCT

CRISPR arrays and Neighbor proteins around NZ_LN831790_6

CRISPR arrays

The CRISPR arrays of NZ_LN831790_6

>merge|NZ_LN831790|6|4180718-4180867|CRISPRCasFinder
CGGTGGCGGCGCGTGGTTCCGCGGCGGGACCCGGAGCGGTGGCGGCGCGTGGTTCCGCGGCGGGACCCGGAGCGGTGGCGGCGCGTGGTTCCGCGGGGGCGTACGGCCCCGAGGCGGCGTACAGCTCCGTGGCGGCGCCCGGACCGGTGG

>NZ_LN831790|6|6|4180718-4180867|CRISPRCasFinder
CGGTGGCGGCGCGTGGTTCCGCGG	CGGGACCCGGAGCGGTGGCGGCGCGTGGTTCCGCGGCGGGACCCGGAG
CGGTGGCGGCGCGTGGTTCCGCGG	GGGCGTACGGCCCCGAGGCGGCGTACAGCT
CCGTGGCGGCGCCCGGACCGGTGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_079164077.1|4172204_4173626_-|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl|CDD|237001
NZ_LN831790.1|WP_029385143.1|4184724_4185822_-|potassium-channel-protein	unknown	unknown	gnl|CDD|367001
NZ_LN831790.1|WP_029385144.1|4183812_4184661_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|366444
NZ_LN831790.1|WP_029384361.1|4174619_4175843_-|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	unknown	unknown	gnl|CDD|213783
NZ_LN831790.1|WP_047121894.1|4177590_4179204_-|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_LN831790.1|WP_029384157.1|4190921_4192082_-|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	unknown	unknown	gnl|CDD|213783
NZ_LN831790.1|WP_029384158.1|4189920_4190925_-|alpha-ketoacid-dehydrogenase-subunit-beta	unknown	unknown	gnl|CDD|223101
NZ_LN831790.1|WP_029381528.1|4171196_4172096_+|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl|CDD|224600
NZ_LN831790.1|WP_157840719.1|4181178_4181604_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029384367.1|4179839_4180385_-|bacterial-proteasome-activator-family-protein	unknown	unknown	gnl|CDD|378489
NZ_LN831790.1|WP_047121895.1|4188433_4189921_-|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl|CDD|237001
NZ_LN831790.1|WP_029381529.1|4170327_4170978_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224715
NZ_LN831790.1|WP_029384364.1|4176994_4177423_+|hypothetical-protein	unknown	unknown	gnl|CDD|214840
NZ_LN831790.1|WP_029385145.1|4182775_4183816_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|130256
NZ_LN831790.1|WP_162183959.1|4173636_4174602_-|alpha-ketoacid-dehydrogenase-subunit-beta	unknown	unknown	gnl|CDD|223101
NZ_LN831790.1|WP_029381530.1|4169032_4170331_-|MFS-transporter	unknown	unknown	gnl|CDD|349949
NZ_LN831790.1|WP_047122556.1|4187395_4188340_-|molybdenum-cofactor-guanylyltransferase	unknown	unknown	gnl|CDD|133000
NZ_LN831790.1|WP_029385141.1|4185818_4187399_-|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl|CDD|238452
NZ_LN831790.1|WP_029384363.1|4176196_4176853_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_LN831790.1|WP_029385146.1|4181624_4182605_-|NAD(P)H-quinone-oxidoreductase	unknown	unknown	gnl|CDD|176180

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_079164077.1|4172204_4173626_-|2-oxo-acid-dehydrogenase-subunit-E2	gnl|CDD|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	1.12583e-164
NZ_LN831790.1|WP_029385143.1|4184724_4185822_-|potassium-channel-protein	gnl|CDD|367001	pfam02254, TrkA_N, TrkA-N domain. This domain is found in a wide variety of proteins. These protein include potassium channels, phosphoesterases, and various other transporters. This domain binds to NAD.	7.94035e-23
NZ_LN831790.1|WP_029385144.1|4183812_4184661_+|ABC-transporter-permease	gnl|CDD|366444	pfam01061, ABC2_membrane, ABC-2 type transporter.	8.20968e-23
NZ_LN831790.1|WP_029384361.1|4174619_4175843_-|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].	0
NZ_LN831790.1|WP_047121894.1|4177590_4179204_-|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	7.84227e-121
NZ_LN831790.1|WP_029384157.1|4190921_4192082_-|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].	3.23629e-170
NZ_LN831790.1|WP_029384158.1|4189920_4190925_-|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].	2.06747e-157
NZ_LN831790.1|WP_029381528.1|4171196_4172096_+|D-alanyl-D-alanine-carboxypeptidase	gnl|CDD|224600	COG1686, DacC, D-alanyl-D-alanine carboxypeptidase [Cell envelope biogenesis, outer membrane].	9.00899e-57
NZ_LN831790.1|WP_029384367.1|4179839_4180385_-|bacterial-proteasome-activator-family-protein	gnl|CDD|378489	pfam10759, DUF2587, Protein of unknown function (DUF2587). This is a bacterial family of proteins with no known function.	6.67718e-91
NZ_LN831790.1|WP_047121895.1|4188433_4189921_-|2-oxo-acid-dehydrogenase-subunit-E2	gnl|CDD|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	8.90833e-157
NZ_LN831790.1|WP_029381529.1|4170327_4170978_-|GntR-family-transcriptional-regulator	gnl|CDD|224715	COG1802, GntR, Transcriptional regulators [Transcription].	7.00542e-41
NZ_LN831790.1|WP_029384364.1|4176994_4177423_+|hypothetical-protein	gnl|CDD|214840	smart00829, PKS_ER, Enoylreductase. Enoylreductase in Polyketide synthases.	0.00734155
NZ_LN831790.1|WP_029385145.1|4182775_4183816_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|130256	TIGR01188, drrA, daunorubicin resistance ABC transporter ATP-binding subunit. This model describes daunorubicin resistance ABC transporter, ATP binding subunit in bacteria and archaea. This model is restricted in its scope to preferentially recognize the ATP binding subunit associated with effux of the drug, daunorubicin. This transport system belong to the larger ATP-Binding Cassette (ABC) transporter superfamily. The characteristic feature of these transporter is the obligatory coupling of ATP hydrolysis to substrate translocation. The minimal configuration of bacterial ABC transport system: an ATPase or ATP binding subunit; An integral membrane protein; a hydrophilic polypetpide, which likely functions as substrate binding protein. In eukaryotes proteins of similar function include p-gyco proteins, multidrug resistance protein etc. [Transport and binding proteins, Other].	1.0947e-122
NZ_LN831790.1|WP_162183959.1|4173636_4174602_-|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].	3.89299e-159
NZ_LN831790.1|WP_029381530.1|4169032_4170331_-|MFS-transporter	gnl|CDD|349949	cd06174, MFS, Major Facilitator Superfamily. The Major Facilitator Superfamily (MFS) is a large and diverse group of secondary transporters that includes uniporters, symporters, and antiporters. MFS proteins facilitate the transport across cytoplasmic or internal membranes of a variety of substrates including ions, sugar phosphates, drugs, neurotransmitters, nucleosides, amino acids, and peptides. They do so using the electrochemical potential of the transported substrates. Uniporters transport a single substrate, while symporters and antiporters transport two substrates in the same or in opposite directions, respectively, across membranes. MFS proteins are typically 400 to 600 amino acids in length, and the majority contain 12 transmembrane alpha helices (TMs) connected by hydrophilic loops. The N- and C-terminal halves of these proteins display weak similarity and may be the result of a gene duplication/fusion event. Based on kinetic studies and the structures of a few bacterial superfamily members, GlpT (glycerol-3-phosphate transporter), LacY (lactose permease), and EmrD (multidrug transporter), MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement. Bacterial members function primarily for nutrient uptake, and as drug-efflux pumps to confer antibiotic resistance. Some MFS proteins have medical significance in humans such as the glucose transporter Glut4, which is impaired in type II diabetes, and glucose-6-phosphate transporter (G6PT), which causes glycogen storage disease when mutated.	6.23667e-34
NZ_LN831790.1|WP_047122556.1|4187395_4188340_-|molybdenum-cofactor-guanylyltransferase	gnl|CDD|133000	cd02503, MobA, MobA catalyzes the formation of molybdopterin guanine dinucleotide. The prokaryotic enzyme molybdopterin-guanine dinucleotide biosynthesis protein A (MobA). All mononuclear molybdoenzymes bind molybdenum in complex with an organic cofactor termed molybdopterin (MPT). In many bacteria, including Escherichia coli, molybdopterin can be further modified by attachment of a GMP group to the terminal phosphate of molybdopterin to form molybdopterin guanine dinucleotide (MGD). This GMP attachment step is catalyzed by MobA, by linking a guanosine 5'-phosphate to MPT forming molybdopterin guanine dinucleotide. This reaction requires GTP, MgCl2, and the MPT form of the cofactor. It is a reaction unique to prokaryotes, and therefore may represent a potential drug target.	2.90512e-32
NZ_LN831790.1|WP_029385141.1|4185818_4187399_-|molybdopterin-molybdotransferase-MoeA	gnl|CDD|238452	cd00887, MoeA, MoeA family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF), an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MoeA, together with MoaB, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes.	1.43966e-97
NZ_LN831790.1|WP_029384363.1|4176196_4176853_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	7.14202e-67
NZ_LN831790.1|WP_029385146.1|4181624_4182605_-|NAD(P)H-quinone-oxidoreductase	gnl|CDD|176180	cd05276, p53_inducible_oxidoreductase, PIG3 p53-inducible quinone oxidoreductase. PIG3 p53-inducible quinone oxidoreductase, a medium chain dehydrogenase/reductase family member, acts in the apoptotic pathway. PIG3 reduces ortho-quinones, but its apoptotic activity has been attributed to oxidative stress generation, since overexpression of PIG3 accumulates reactive oxygen species. PIG3 resembles the MDR family member quinone reductases, which catalyze the reduction of quinone to hydroxyquinone. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	0

Protein sequences

>NZ_LN831790.1|WP_029384367.1|4179839_4180385_-|bacterial-proteasome-activator-family-protein
MEMPRNDRSPENPQILVVGQDGMALSGGGGGDEDARETPVTEQVEQPAKVMRIGSMIKQLLEEVRAAPLDEASRNRLKEIHASSVKELEDGLAPELVEELERLSLPFTDEGTPSDAELRIAQAQLVGWLEGLFHGIQTTLFAQQMAARAQLEQMRRALPAGLGHDGGEEGLAGGRSGGPYL
>NZ_LN831790.1|WP_047121894.1|4177590_4179204_-|serine/threonine-protein-kinase
MAQQQRAQGPSDPEATGGGMSDAPETWGNGGLVGDGRYRLTHRLGRGGMAEVFAAEDVRLGRTVAVKLLRADLAEDPVSKARFTREAQSVAGLNHHAIVAVYDSGEDFVGGQSVPYIVMELVEGRTIRDLLMNAEAPGPEQALIIVSGVLEALAYSHQHGIVHRDIKPANVIITHNGAVKVMDFGIARALHGASTTMTQTGMVMGTPQYLSPEQALGKAVDHRSDLYATGCLLYELLALRPPFTGETPLSVVYQHVQDIPTPPSEASDGCPPELDGLVMRSLAKEPDDRFQTAEEMRGLVQYALQMLYEQGGHTGTWNTGPVGMHEGRHAPSAGLAGTTVLPHSDHGSGTTQIPQPILPTGYGNDDGGFEGQGNRGSGRGKLWILAVLAVIAIVAGAALAINTTRDDKGEKPGPSKSPSATQSTEEDKPSETPSDGATQDTTDPGTDPGTGGSGGDSGWTQPTAPSYTPSYTPTQEPTQEPTGGESPPPATTEPTDGQPTDGQPTGGASEPSSGDGGDDGGTVTGGPVVDPQIGGSG
>NZ_LN831790.1|WP_029384364.1|4176994_4177423_+|hypothetical-protein
MPSPSDPQLALGLLARTCHGRAATSMRALPFLAFARHIVVDGRVLLRMPGNCGYQQACVGSVVAYGTDNLSSARPGESVWTVQVVGWCEAYEPTAAELELFGPAPARVDGVPFEPAYLRVEPQFGVVHGVDDGPGRRGRATA
>NZ_LN831790.1|WP_029384363.1|4176196_4176853_+|response-regulator-transcription-factor
MREEGQIRVFLLDDHEVVRRGVHDLLAGEDDIEVVGEAGTAADALARIPATRPDVAVLDVRLPDGSGVEVCRDVRSRDESIRCLMLTSFSDDEALFDAIMAGASGYVLKDIRGGELLAAVRDVAAGGSLLDPVATARVLERLRGGGPRTDDRLAHLTEQERRILELIGEGLTNRAIGERLHLAEKTIKNYVSSLLSKLGMQRRSQAAAYVARMQAEDR
>NZ_LN831790.1|WP_029384361.1|4174619_4175843_-|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha
MTVESTAARKPRRSAGSKAGTTGTKAAGTTGTKRTTRTAAKKTAEKSTEPELVQLLTPEGERVENAEYDAYVAGVTPDELRGLYRDMVLTRRFDAEATALQRQGELGLWASLLGQEAAQIGSGRATREDDYVFPTYREHGVAWCRGVDPTNLLGMFRGVNNGGWDPNGNNFHLYTIVIGSQALHATGYAMGIAKDGADSAVIAYFGDGASSQGDVSEAFNFAAVYNAPVVFFCQNNQWAISESNEKQTRVPLYQRAQGFGFPGVRVDGNDVLATLAVTRWALERARRGEGPALIEAWTYRMGAHTTSDDPSRYRHDDERAAWEAKDPILRLRRHLEAAHHADESFFAELEAESEALGKRVREAVRAMRDPDRFAIFENVYADGHALVDEERAQFAAYQASFADAEGV
>NZ_LN831790.1|WP_162183959.1|4173636_4174602_-|alpha-ketoacid-dehydrogenase-subunit-beta
MALAKAINESLRRALETDPKVLVMGEDVGKLGGVFRVTDGLQKDFGENRVIDTPLAESGIVGTAIGLALRGYRPVVEIQFDGFVFPAYDQIVTQLAKMHARSLGTVKLPVVIRIPYGGGIGAVEHHSESPEALFAHVAGLKVVSPSNASDAYWMMQQAIQSDDPVIYFEPKRRYWDKGEVSTEAIPGPLHAARVVREGTDLTLAAYGPMVKLCQEVADAAAEEGRSLEVLDLRSVSPLDFDAIQTSVEKTRRLVVVHEAPVFFGSGAEIAARITERCFYHLEAPVLRVGGYHAPYPPARLEEEYLPDLDRVLDAVDRSLAY
>NZ_LN831790.1|WP_079164077.1|4172204_4173626_-|2-oxo-acid-dehydrogenase-subunit-E2
MTTMTEGSVREFKMPDVGEGLTEAEILKWYVQPGDTVTDGQVVCEVETAKAAVELPIPYDGVVRELRFPEGTTVDVGTAIITVDVGGPAEPAAPEPAPAAPERGEEPAPQGRQPVLVGYGVAASSTRRRPRKAAGAPAQEASAAQAAPAAVVAVQAELNGHGPADRRRPLAKPPVRKLAKDLGVDLATVTPTGPDGVITREDVHAAAAPQAVPQQATAPEPVAPAPVAAPAAPAPVTYDTARETRIPVKGVRKATAAAMVGSAFTAPHVTEFVTVDVTRTMKLVEELKQDKEFAGLRVNPLLLIAKALLVAVKRNPDINASWDEAAQEIVVKHYVNLGIAAATPRGLIVPNIKDAHAKTLPQLAQALGELVTTAREGKTSPAAMQGGTVTITNVGVFGVDTGTPILNPGESAILAVGAIKPQPWVHKGKVKPRQVTTLALSFDHRLVDGELGSKVLADVAAVLEQPKRLITWA
>NZ_LN831790.1|WP_029381528.1|4171196_4172096_+|D-alanyl-D-alanine-carboxypeptidase
MKIGIQGIRLHRAAAVAVTTGAMLATGALSAAPAQAATAPTIAAKGGFVMNNATGKSLYTKAADTKRSTGSTTKIMTAKVVLSQPNLNLDAKVTIQKAYSDYIVSKTASSARLIVGDKVTVRQLLYGLMLPSGCDAAYALADKFGTGSTRAARVKSFIGKMNTTAKSLGLKNTHFDSFDGIGNGANYSTPRDLTKLASSAMKSSTFRTIVKTKKYTAKTVTKTGSTRTMAPWVNTNTLLNNYSGTIGVKTGSGPEAKYCLVFAATRNGKTVIGTVLASTSATQRETDAKKLLTYGFSRA
>NZ_LN831790.1|WP_029381529.1|4170327_4170978_-|GntR-family-transcriptional-regulator
MTLAVKQPPAADRVYTHVKQGVLERRYEGGTLLTEGELAEAVGVSRTPVREALLRLEVEGLLRLYPKKGALVLPVSAQEIADVVETRLLVEEHAARKAVPAPPGLVERLEHLLARQKEQAAAGDLAAAAVTDRCFHAEIVRSGGNEILSKLYDQLRDRQLRMGVAVMHSHPDRIAKTLAEHGEILDALRAGDAEAAVAVVHRHVSWFSHLARGEVR
>NZ_LN831790.1|WP_029381530.1|4169032_4170331_-|MFS-transporter
MSGNTTLPADPPGGRRAIAVWSVGVAVYFVAVIFRTSLGVAGLDAADRFHVGASALSTFSILQLLVYAGMQIPVGLLVDRLGTKKVLGLGVVLFTAGQLGFAFSPSYGMALASRALLGCGDAMTFISVLRLGTRWFPARRGPLVGQLAGLAGMAGNLVSTLVLARLLHGIGWTAAFAGSALAGVAVFVLLLLFLKDHPEGYEPEPPGHQGAAYVRRQIVRSWREPGTRLGLWVHFTTQFPGMVFLLLWGLPFLVEAQGLTRATAGELLTLVVLSNMAVGLVYGQVVARHHGARLPLALGTVGATAVLWAATLAWPGAHAPMGLLIALCVVLGACGPASMIGFDFARPANPPERQGTASGITNMGGFVASMTTLFAIGVLLDATGDDYTVAFSSVFVLQALGVVQILRLRRRAARRERERLVASRVETVHVPA
>NZ_LN831790.1|WP_157840719.1|4181178_4181604_+|hypothetical-protein
MGGTARKPSPARSAPAPAAEPSRAGSRPGQGRERPGRRDGPGTEKGALTDADPAYPNGPAEDGGIMPGRPDLSVPAWETGPGPAAPPVRQREPAVARAEGSAGPASRLLPLGSGLVLIGLGLGLALFALRLRRSQRAQQAG
>NZ_LN831790.1|WP_029385146.1|4181624_4182605_-|NAD(P)H-quinone-oxidoreductase
MHAITIPEPGGPEALVWDEVPDPVPGEGEVLVEVVASAVNRADIMQRQGFYDPPPGAPRHPGLECSGRIAALGPGVTGWSVGDEVCALLGGGGYAQKAAVPAGQLLPVPDGVGLKEAAALPEVVCTVWSNVFMVAHLRPGETLLVHGGSSGIGTMAIQLAKAVGAKVAVTAGTEEKLERCAELGADILINYREQDFVAEIKRATDGAGADVILDNMGAKYLDRNVQALAVNGRLAIIGLQGGTKGELNIGALLAKRAAVSATSLRARPLEEKTAIVAAVREHVWPLFAAGRVRPVVDREMPMSEASAAHRVVEESGHIGKVLLVTS
>NZ_LN831790.1|WP_029385145.1|4182775_4183816_+|ATP-binding-cassette-domain-containing-protein
MSTQTSGPAIETAGLVKTFGVTRALDGVDLVVPTGTVYGVLGPNGAGKTTAVRILATLLRPDGGEAHVFGHDVVHAADEVRGRVSLTGQYASVDEDLTGTENLVLLGRLLGHRKKAARDRAAQLLDAFGLTEAAGKQVKHYSGGMRRRIDIAASILNTPDLLFLDEPTTGLDPRSRNQVWDIVRAVVAQGTTVLLTTQYLDEADQLASRIAVIDKGRVIAEGTKGELKASVGAGSVHLRLRDARQRPDAERVLRTALLAEVQREPDPLALTARLVAASATAADQAARALGELTRAGITVDNFSLGQPSLDEVFLALTGHGTGRRGTGRDAGSPGTGPDTKEGEVPA
>NZ_LN831790.1|WP_029385144.1|4183812_4184661_+|ABC-transporter-permease
MSTAASTESRELTPVSAESLAALLVARKRPPRPSSLSTSLTFGWRAVLKIKHVPEQLFDVTAFPIMNLLMFTYLFGGALAGSPGDYIQFVLPGILVMSVVMITMYTGVSVNTDIEKGVFDRFRSLPIWRPSAMVGYLLGDALRYTIASVVMLTVGLVLGYRPGGGAGGVVAGIALLLVFSFAFSWIWTMFGLMLRTEKSVMSTSMMVIFPLTFLSNVFVDPKTMPGWLQVFVNNSPITHLASAVRGLMAGDWPAGEIAWSLGWTAFFVVVFGPVTMRLYNRK
>NZ_LN831790.1|WP_029385143.1|4184724_4185822_-|potassium-channel-protein
MKLPGQDAIARQADEHLVTHRVSLPRRVVERPIRQVAKRLAMALFVLVLTALLVYADNDGYNDNSDGAVDFLDAWYYATVTLSTTGYGDITPVSDGARLTNIFVITPLRVMFLIILVGTTLEVLTERTREEWRLNRWRSMLRDHTVVIGFGTKGRSALQTVCATGLKKEQVVVVDPSGKVIDAANADGFVGVVGDATRSDVLKRAEVHKARQIIIATQRDDTAVLVALTARQLNRGAKIVAAVREEENAPLLKQSGADVVITSASAAGRLLGLSVLSPAAGMVMEDLIHQGSGLDIVERPVIKAEVGKSPREVDSLVVSVVRGHRVLGYDDPAVARLELTDRLITIVRATPGRQVAPDARPLPRD
>NZ_LN831790.1|WP_029385141.1|4185818_4187399_-|molybdopterin-molybdotransferase-MoeA
MTAHGTSTGRDAEDAEGLDVEEVLALVNDDRGPRPADRLPGPAAPAAGADPAGRGHAPRGDHETGGDHGGHRTDDGHESPGGRDGRDGRESPGGRENHDAHDAHHAQDPHGAHRGRGPRTHGATPWPGAREIAASAARAAVRSSPPPPVSVPLDGALGLTLAEPLTALTDLPSFDTSAMDGWAVAGPGPWDVREDGVLAGHTGHRPLGDGEAVRIATGARIPEDTTAVLRTEHGRTDGRGRLHAVPRDRAIVPGQDIRPRGQECRSGDRLLPAGTLVTPAVLGLAAAAGYDRLRAVPRPRVDVLVLGDELLTEGLPHDGLIRDALGPMLPPWLRALGADVTSVRRIGDDAEALHTAVTTSAADVVVTTGGTAAGPVDHLHPTLRRIGAELLVDGVEVRPGHPMLLARIGEGRHLVGLPGNPLAAVSGLLTLAEPLLRTLAARPAPEPYGVPLQEPVQGHPYDTRLVPVVLRGDRAVPLHYNGPAMLRGIAVADALAVVPPGGARPGEETELLDLPWTTGGIGVCFT
>NZ_LN831790.1|WP_047122556.1|4187395_4188340_-|molybdenum-cofactor-guanylyltransferase
MLAGGSARRLGGADKPGVRVGGRPLLDRVLAACAGARTTVVVADPRPVPRAVTWAREDPPGAGPLAALDAGLRHTTAEHVVVLSADLPFLAGTAVRGLLAALPGSDADGVLCTDADGRDQPLVAAYRARALRRGLAALAAGHGGLTGLPLRRLTAGLRLARIADPVASFDCDTWDDIATARARIREHGHVLDEWISTVKDELGIDLDVDTGVLLDLARDAAHGVARPAAPLTTFLVGYAAGRAGGDPRAVAEAARKATALALRWAEEEEETAGTADTPSGTTGTDGAASHGAASGATAPDAAPDAAPGIRPDAG
>NZ_LN831790.1|WP_047121895.1|4188433_4189921_-|2-oxo-acid-dehydrogenase-subunit-E2
MAQVLEFKLPDLGEGLTEAEIVRWLVEVGDVVAVDQPVVEVETAKAMVEVPCPYGGVVTARFGEAGSELPVGAPLLTVAVGEPEPDRPAAPGADGHRAQPARAQAVSAASAEAGSAASGGAGPSAGAEDPGTEGSGNVLVGYGTSGAPARRRRVRPGPPAGANGRARAADPVDGPVPVISPLVRRLARENGLDLRELTGSGPDGLILRADVEYALRAAAAQGRTATAPAGPRPGGEPAREAAGAAPAPQAGAAALGAAPLTAAPGADGVRTPLKGVRGAVADKLSRSRREIPDATCWVDADATELMRARAAMNAAGVPKVSLIALLARICTAALARFPELNSTVDTEAREIVRFERVHLGFAAQTERGLVVPVVRDAHARNAESLTAEFARLTEAARTGALTPAELTGGTFTLNNYGVFGVDGSTPILNHPEAAMLGVGRITPKPWVHEGELAVRQVVQLSLTFDHRVCDGGTAGGFLRYVADCVEQPAVLLRTV
>NZ_LN831790.1|WP_029384158.1|4189920_4190925_-|alpha-ketoacid-dehydrogenase-subunit-beta
MSTVAVRPATMAQALTRALRDAMAADDSVHVLGEDVGALGGVFRVTDGLAEEFGEDRCTDTPLAEAGILGTAVGMAMYGLRPVVEMQFDAFAYPAFEQLVSHVSRMRNRTRGAMPLPLTVRVPYGGGIGGVEHHSDSSEAYYMATPGLHVVTPATVADAYGLLRAAIASDDPVVFLEPKRLYWSKDSWNPEDPAPVEPIGRAVVRRSGRSATLITYGPSVAVCMEAAEAARAEGWDLEVVDLRSLVPFDDETVCASVRRTGRAVVVHESGSFGGPGGEIAARVTERCFHHLEAPVLRVAGFDVPYPPPMLERHHLPGVDRILDAVGRLQWEAES
>NZ_LN831790.1|WP_029384157.1|4190921_4192082_-|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha
MTVMDQRGAYRPSPPPAWQPRTDPAPLLPDPEPYRVLGTEAAGQADPELLRTLYAHLVRGRRYNAQATALTKQGRLAVYPSSTGQEACEVAAALALKEQDWLFPSYRDTLAVVARGVDPVQALTLLRGDWHTGYDPREHRVAPLCTPLATQLPHAVGLAHAARLKGDDVVALAMVGDGGTSEGDFHEALNFAAVWQAPVVFLVQNNGFAISVPLAKQTAAPSLAHKAVGYGMPGRLVDGNDAAAVHEVLTDAVRHARAGGGPTLVEAITYRVDAHTNADDATRYRGDAEVDTWREHDPILLLERELTARGLLDEDAMRAAREDAEAMAADLRARMHQDPVLDPMDLFDHVYAEPTPQLREQRAQLRAELEAEAEAGPAPRPEGALR

Crispr_ID: NZ_LN831790_7

• CRISPR_ID: NZ_LN831790_7
• CRISPR_location: 4377001-4377098
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_7

Consensus_repeat	Method
CCCGGAGCGGGTCCGGTGGCCCGC	CRISPRCasFinder

spacers of NZ_LN831790_7

>7.1|4377025|50|NZ_LN831790|CRISPRCasFinder
TGTCCCGGCGGCCCCCGGAGCGGGTCCGGTGGCCCGCTGTCCCGGCGGCC

CRISPR arrays and Neighbor proteins around NZ_LN831790_7

CRISPR arrays

The CRISPR arrays of NZ_LN831790_7

>merge|NZ_LN831790|7|4377001-4377098|CRISPRCasFinder
CCCGGAGCGGGTCCGGTGGCCCGCTGTCCCGGCGGCCCCCGGAGCGGGTCCGGTGGCCCGCTGTCCCGGCGGCCCCCGGAGCGGGTCCGGCGGCCCGC

>NZ_LN831790|7|7|4377001-4377098|CRISPRCasFinder
CCCGGAGCGGGTCCGGTGGCCCGC	TGTCCCGGCGGCCCCCGGAGCGGGTCCGGTGGCCCGCTGTCCCGGCGGCC
CCCGGAGCGGGTCCGGCGGCCCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029384488.1|4387379_4388081_+|GAF-and-ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|377145
NZ_LN831790.1|WP_029385457.1|4377931_4379506_+|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831790.1|WP_029385463.1|4373549_4373933_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831790.1|WP_047121917.1|4380809_4382969_+|glycosyltransferase-family-39-protein	unknown	unknown	gnl|CDD|379080
NZ_LN831790.1|WP_029385458.1|4377194_4377935_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831790.1|WP_029384495.1|4383066_4384581_+|MFS-transporter	unknown	unknown	gnl|CDD|184957
NZ_LN831790.1|WP_029384490.1|4386590_4387361_+|ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|377145
NZ_LN831790.1|WP_029385464.1|4373045_4373447_-|RidA-family-protein	unknown	unknown	gnl|CDD|100004
NZ_LN831790.1|WP_029384327.1|4364845_4366060_-|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_LN831790.1|WP_029384494.1|4384697_4385453_+|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|367243
NZ_LN831790.1|WP_029384492.1|4385500_4385971_-|PPOX-class-F420-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274679
NZ_LN831790.1|WP_078648320.1|4371704_4372268_-|hypothetical-protein	unknown	unknown	gnl|CDD|366264
NZ_LN831790.1|WP_157840704.1|4365959_4366406_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380057
NZ_LN831790.1|WP_029384325.1|4362497_4363058_+|SigE-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|132028
NZ_LN831790.1|WP_029385459.1|4375968_4376841_+|DUF2797-domain-containing-protein	unknown	unknown	gnl|CDD|378524
NZ_LN831790.1|WP_029384491.1|4386027_4386381_-|STAS-domain-containing-protein	unknown	unknown	gnl|CDD|132914
NZ_LN831790.1|WP_079164078.1|4366580_4371458_-|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|223021
NZ_LN831790.1|WP_029385456.1|4379520_4380813_+|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	unknown	unknown	gnl|CDD|133031
NZ_LN831790.1|WP_029385462.1|4374042_4375170_+|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133382
NZ_LN831790.1|WP_029384326.1|4363138_4364815_+|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|341284

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029384488.1|4387379_4388081_+|GAF-and-ANTAR-domain-containing-protein	gnl|CDD|377145	pfam03861, ANTAR, ANTAR domain. ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	1.45968e-12
NZ_LN831790.1|WP_029385457.1|4377931_4379506_+|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.64245e-60
NZ_LN831790.1|WP_029385463.1|4373549_4373933_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	1.6653e-34
NZ_LN831790.1|WP_047121917.1|4380809_4382969_+|glycosyltransferase-family-39-protein	gnl|CDD|379080	pfam13231, PMT_2, Dolichyl-phosphate-mannose-protein mannosyltransferase. This family contains members that are not captured by pfam02366.	1.88396e-29
NZ_LN831790.1|WP_029385458.1|4377194_4377935_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	8.54727e-83
NZ_LN831790.1|WP_029384495.1|4383066_4384581_+|MFS-transporter	gnl|CDD|184957	PRK14995, PRK14995, SmvA family efflux MFS transporter.	6.8324e-69
NZ_LN831790.1|WP_029384490.1|4386590_4387361_+|ANTAR-domain-containing-protein	gnl|CDD|377145	pfam03861, ANTAR, ANTAR domain. ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	7.75534e-15
NZ_LN831790.1|WP_029385464.1|4373045_4373447_-|RidA-family-protein	gnl|CDD|100004	cd00448, YjgF_YER057c_UK114_family, YjgF, YER057c, and UK114 belong to a large family of proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	3.50524e-24
NZ_LN831790.1|WP_029384327.1|4364845_4366060_-|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.29178e-48
NZ_LN831790.1|WP_029384494.1|4384697_4385453_+|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein	gnl|CDD|367243	pfam02909, TetR_C, Tetracyclin repressor, C-terminal all-alpha domain.	3.93698e-12
NZ_LN831790.1|WP_029384492.1|4385500_4385971_-|PPOX-class-F420-dependent-oxidoreductase	gnl|CDD|274679	TIGR03618, Rv1155_F420, PPOX class probable F420-dependent enzyme. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomyces, make F420. The Partial Phylogenetic Profiling algorithm identifies this members of this protein family as high-scoring proteins to the F420 biosynthesis profile. A member of this family, Rv1155, was crytallized after expression in Escherichia coli, which does not synthesize F420; the crystal structure shown to resemble FMN-binding proteins, but with a recognizable empty cleft corresponding to, yet differing profounding from, the FMN site of pyridoxine 5'-phosphate oxidase. We propose that this protein family consists of F420-binding enzymes. [Unknown function, Enzymes of unknown specificity].	5.43321e-40
NZ_LN831790.1|WP_078648320.1|4371704_4372268_-|hypothetical-protein	gnl|CDD|366264	pfam00720, SSI, Subtilisin inhibitor-like.	2.32246e-05
NZ_LN831790.1|WP_157840704.1|4365959_4366406_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|380057	pfam17926, TetR_C_21, Tetracyclin repressor-like, C-terminal domain. TetR family regulators are involved in the transcriptional control of multidrug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. The TetR proteins identified in overm ultiple genera of bacteria and archaea share a common helix-turn-helix (HTH) structure in their DNA-binding domain. However, TetR proteins can work in different ways: they can bind a target operator directly to exert their effect (e.g. TetR binds Tet(A) gene to repress it in the absence of tetracycline), or they can be involved in complex regulatory cascades in which the TetR protein can either be modulated by another regulator or TetR can trigger the cellular response. TetR regulates the expression of the membrane-associated tetracycline resistance protein, TetA, which exports the tetracycline antibiotic out of the cell before it can attach to the ribosomes and inhibit protein synthesis. TetR blocks transcription from the genes encoding both TetA and TetR in the absence of antibiotic. The C-terminal domain is multi-helical and is interlocked in the homodimer with the helix-turn-helix (HTH) DNA-binding domain. This entry represents the C-terminal domain present the TetR Transcriptional Repressor found in Streptomyces coelicolor A3. Family members include HTH-type transcriptional repressor sco4008, which is suggested to be a transcriptional repressor of sco4007 responsible for the multidrug resistance system in S. coelicolor A3.	2.19299e-26
NZ_LN831790.1|WP_029384325.1|4362497_4363058_+|SigE-family-RNA-polymerase-sigma-factor	gnl|CDD|132028	TIGR02983, putative_RNA_polymerase_ECF-subfamily_sigma_factor, RNA polymerase sigma-70 factor, sigma-E family. This group of similar sigma-70 factors includes the sigE factor from Streptomyces coelicolor. The family appears to include a paralagous expansion in the Streptomycetes lineage, while related Actinomycetales have at most two representatives.	4.247e-59
NZ_LN831790.1|WP_029385459.1|4375968_4376841_+|DUF2797-domain-containing-protein	gnl|CDD|378524	pfam10977, DUF2797, Protein of unknown function (DUF2797). This family of proteins has no known function.	5.36376e-45
NZ_LN831790.1|WP_029384491.1|4386027_4386381_-|STAS-domain-containing-protein	gnl|CDD|132914	cd07043, STAS_anti-anti-sigma_factors, Sulphate Transporter and Anti-Sigma factor antagonist) domain of anti-anti-sigma factors, key regulators of anti-sigma factors by phosphorylation. Anti-anti-sigma factors play an important role in the regulation of several sigma factors and their corresponding anti-sigma factors. Upon dephosphorylation they bind the anti-sigma factor and induce the release of the sigma factor from the anti-sigma factor. In a feedback mechanism the anti-anti-sigma factor can be inactivated via phosphorylation by the anti-sigma factor. Well studied examples from Bacillus subtilis are SpoIIAA (regulating sigmaF and sigmaC which play an important role in sporulation) and RsbV (regulating sigmaB involved in the general stress response). The STAS domain is also found in the C- terminal region of sulphate transporters and stressosomes.	2.74127e-14
NZ_LN831790.1|WP_079164078.1|4366580_4371458_-|PAS-domain-S-box-protein	gnl|CDD|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	7.40833e-19
NZ_LN831790.1|WP_029385456.1|4379520_4380813_+|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	gnl|CDD|133031	cd04188, DPG_synthase, DPG_synthase is involved in protein N-linked glycosylation. UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate.	3.09593e-81
NZ_LN831790.1|WP_029385462.1|4374042_4375170_+|MerR-family-transcriptional-regulator	gnl|CDD|133382	cd01107, HTH_BmrR, Helix-Turn-Helix DNA binding domain of the BmrR transcription regulator. Helix-turn-helix (HTH) multidrug-efflux transporter transcription regulator, BmrR and YdfL of Bacillus subtilis, and related proteins; N-terminal domain. Bmr is a membrane protein which causes the efflux of a variety of toxic substances and antibiotics. BmrR is comprised of two distinct domains that harbor a regulatory (effector-binding) site and an active (DNA-binding) site. The conserved N-terminal domain contains a winged HTH motif that mediates DNA binding, while the C-terminal domain binds coactivating, toxic compounds. BmrR shares the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements.	7.44286e-28
NZ_LN831790.1|WP_029384326.1|4363138_4364815_+|long-chain-fatty-acid--CoA-ligase	gnl|CDD|341284	cd12119, ttLC_FACS_AlkK_like, Fatty acyl-CoA synthetases similar to LC-FACS from Thermus thermophiles. This family includes fatty acyl-CoA synthetases that can activate medium-chain to long-chain fatty acids. They catalyze the ATP-dependent acylation of fatty acids in a two-step reaction. The carboxylate substrate first reacts with ATP to form an acyl-adenylate intermediate, which then reacts with CoA to produce an acyl-CoA ester. The fatty acyl-CoA synthetases are responsible for fatty acid degradation as well as physiological regulation of cellular functions via the production of fatty acyl-CoA esters. The fatty acyl-CoA synthetase from Thermus thermophiles in this family catalyzes the long-chain fatty acid, myristoyl acid, while another member in this family, the AlkK protein identified from Pseudomonas oleovorans, targets medium chain fatty acids. This family also includes uncharacterized FACS proteins.	0

Protein sequences

>NZ_LN831790.1|WP_029385459.1|4375968_4376841_+|DUF2797-domain-containing-protein
MAQAWRCSGLRWSSRGPELAWVGGRRSALTWGKRVAFGVAEGGVRTCVGARGHACPLRAAVAGRSTGARCDQCARLDRAHSVAADTLADDPRPYHVYLAWFGPGRAKVGITALERGSARLLEQGAICFGWLGRGPLMAARRAEELLRAALGVPDRIPYAEKRAVRSALPDTAAERAAELAELHARAVALGGWPEALTPEPFRPVDHVGVFGLAGVPDAIGEVTELVPGGTVSGELVAAAGPDLHLATRRGVVVLDTRLLAGWHLVPAEGEGTAVPVRAYRAAPGTQDGLF
>NZ_LN831790.1|WP_029385462.1|4374042_4375170_+|MerR-family-transcriptional-regulator
MDDDSDALMNIGTFARRVGLAPSALRFYDDCGVLPPVRVDGVTGYRYYAPGQEARAVLVRRMREAGMPLTDVCQVLDGSGERARAVLEAHVRRVRETAEAARSAVEEILRDLLDLEGAGGPVGGGRGARARIGGAELAGAVRQVAPAAADPAVCEEFPVLGCVLVELDGQEVRLVATDRYRLAVRALRPSSSAGEPRRILVRVPDLREAAAWALRRAEAVVEIGPGGARLRDGDAPDESWELPAVPGTFPDYRQVLDALPAVRHRIVTDRAALGAALAEVEAEAGGPVTVRAGRDRLALVPRGSGARELAAVCTGAPVPRVAFDPGVLLPAVEAGVGPDVLLEFASPDLPVLVRSADQGSFSTLVMPVRADPADG
>NZ_LN831790.1|WP_029385463.1|4373549_4373933_+|helix-turn-helix-transcriptional-regulator
MVTKRLLKGLPEDADLRRADSLAREIFSDVANKWALLIIEALGERTLRFSELRGEVEGISHKMLTQNLRMLERNGLVDRKVHPTVPPRVEYTLTEPGRALRTAVDALCGWTHQHLAHIERARGRFDA
>NZ_LN831790.1|WP_029385464.1|4373045_4373447_-|RidA-family-protein
MTTIDVFHYGVPAEKDFGYAQAIKSGDLVHVSGQLSFDEAGEFVHAGDFAAQLTRTYANMDRILDHYGATRNQIVSQTLYLVNLRQNAAATAEGNLGYFGDHRPASTVLGVTELTLPGQLVEISFVIDTKLPA
>NZ_LN831790.1|WP_078648320.1|4371704_4372268_-|hypothetical-protein
MSQVISYIARRAGRQAPPRPESRRPRLALRRLLVTAASSLTAVASLAAGPSTAYAAPATGAPSTTPVAQAPVRHSGDHLTVTVRNAGKGRDGTFELYCHPGGGSHPDPEGACAVVERNTRWGQDVFAPAARGGACTMQYGGPATARVTGTWAGRPVDATYDRRDGCAISRWDRMVPLLPDLGSTASS
>NZ_LN831790.1|WP_079164078.1|4366580_4371458_-|PAS-domain-S-box-protein
MSSRPSRGAARLAAILDALPDALVLVNANGTVVNANTIALETFETPGTALVGRGLLDLLPQFDSKLIPGSMRRPDHLDPRARTKPTRMIARRTDGTEFPVEVTSANLENGQQAYDGYGYTGDELLMLVVRDLSGTVDTEAELARSQRQTEMILRAASEGVVGTDTDGRIVLVNPAAAQILGYRAGELGGRELHTLILHSRADGSPFPYDESPLADTLRSGRKHRVRGQVVYAKNGDKVPVDLTTAPVRDGDQLVGAVMTFADRRPYEALVKERKDAEQRHAEELERVAEEHASELTALRQKHVTEVEELREKHAEELAAGEERYAALGEREKDRYEALAARHEQLLTLLGVSLRGPLEELRRELSALAADDAGQLWPEANQVLHHLSAGYSRITTLIDNVLGYQRLDTGAEGLSRTKVMLDAVVTAGVDGAVELVGPGRVQFAVHAPPIEAEVDPRLLATALAHLVADVAGVDATGNAPVSATGYMDSTVVVAAAQRGEVVRIEVRGPYAGGDPVHEPIVRGIVRAHGGVLQTHEVPGMSGSAYVLEVPIGAGAGAVAAGTGPAAEAAAPGAAPETGAESGPAGEPAEGAARPALAPPAPAAEAGGAGEQTGGGRRRARRVDAFLESDLAGPGGDADGSGVPGAEGEGGVPTGRRRRRAAEAPAPVPVPAAPLPGEVPGGTGRRRRRPSDDADAAAGQGSGVAEGAVVTAAEHAAGTAASGTGLGGTVPPQGVPAPSGRRARRPADDQHALPPALPAPSGEADPSAPDDPSRPTGRRRRALASAAERAAAQEAGPRQVFALPPAEADRPAGAAGGVRPVDAPAAPATPVAPGAGGPQVPQVPQSPRGPVPAGAEGPAAPEPSASAAAPGADIPAQARGHRPAHGTDAAGAAGAMPSGAGASGAGASGDGQAGEGRHDAVPHDQSVGHTAPQPHPVTDSTGRRRRPVAVPPGAPAPAVPPAGTQGQGVAVPAQGVPVQDTAGRGVPLAAQGGAAARATARTTGEVPGRIPAPIPGQAPEQAPGRVPGQIPAPAPASAAVPGRTPEQAAEAPSAGQAQPQGGPAPTPPNTPTAPNTPTAPTAPTTTGQAGQAGQTAGQTGQTVRQAGLPAQQSGTIAQPLPQPQAASRPPQQVPDEAVAGRPAPAAQAVPVPQPWPVAGETPVPGTPVPPDGAANAVPAHGTAAPVPPGEVPQESRGAGAAAPVPPAAPVPVPGAPLPGTAPLPPETPRPAQPLPAEAAVPVDPNSTQGRSISVRTLGQGVPFTRQAAQVQQPSATPAPHQPGGSGRRRKLGTPPDPAAARPEQGARPHPAAEQTPAQPRTPGQPQPGAPAPAGQPPRLAQASEGAGRSYAIGAPDENAAEGPEPLDGPGGAVEVADTPRPQPLDDELPPEPLDNPRRLLVWPAPDVSTQQALSDRGYRPVIVHSREEVDAQIAAFPAALFVDPLTGPITRTALQSLRQAAVAAEVPVLVTAGLGQASRDAAYGADPAVLLKALAPRDSEQHPPRVLLIEEHPEIALALTATLERRGMHVARAASDADAVALATQFRPNLVVMDLMRVHRRQAGIVDWLRANGQLNRTPLVVYTAAVDPADLPRLASGETVLFLAERSTSTEVQSRIVDLLARIGTN
>NZ_LN831790.1|WP_157840704.1|4365959_4366406_+|TetR/AcrR-family-transcriptional-regulator
MRARKSNKAELFTQVLGRCMVDLAAAVPVDPDDIDGWLDRLMDYHAAHPELLRLLFWEGIEYGTAELPDEAARQQHYAEKVAAVADSQARGVISDAIPARDLLFLLIAMANYATFVPQMSRILVGGEEAARDRLRESVKEAARRLVAT
>NZ_LN831790.1|WP_029384327.1|4364845_4366060_-|MFS-transporter
MSSGSTGTAAARSTIQRPSTWVNSSALLLFLALIAVCTAVTAANIYLAAPLLPLIARDYGSTAPAVAWIASVAQGGYAVGLLFFAPLGDSANRRRLVGALTVVTAVALIGAAAAPGTAALAVAVFVAAAATVIPQLLVPLVAERAPADRRARHVAAVIAGLFTGIVAARVLGGLAGQAFGWRWVFAGSAVLTLLLGLATARALPSERRLGAPSFLAGIAALPGLLRRSPDLWRACVRQAGMYGAWSAVWTSLALLLTGPAYGLSTAAAGLFGLFGLTASAVAPLAGGMVDRFGAAKVVRTAFLVAAVSVPLFWLGGHVLVALFAAAVAIHAALVASHVANQTLALTTTATPAAANTAYVVSGFAGGALASALAGPAFGHLGWHGVCAVAGVWLLLGWAATAVRR
>NZ_LN831790.1|WP_029384326.1|4363138_4364815_+|long-chain-fatty-acid--CoA-ligase
MSPREDAVLSTMQDVPLLISRILTHGAAVHGTSQVTTWTGEGEPHRRSFAEIGARAAQLAHALRADLQVTGDERVATLMWNNAEHVEAYFAIPSMGAVLHTLNLRLPPEQLVWIVRHAADRVVIANGSLLPLLAPLLPHLETVEHLVVSGPGDRSLLAGAPVRVHEYEELIAGKPTAYDWPELDERTAAAMCYTSGTTGDPKGVVYSHRSVYLHSMQVNMAQSMGLTDADTSLVVVPQFHVNAWGLPHATFMTGVNLLMPDRFLQPAPLAEMIESERPTHAAAVPTIWQGLLAELTAKPRDVSSLTQVTIGGSACPPSLMEAFDRLGMRVCHAWGMTETSPLGTVARPPAHAAGTEAEFGYRLTQGRFPAGVEARLTGPGGERLPWDGESAGELEVRGPWIAGAYYNGPGAEPLRPDDKFSEDGWLKTGDVGTISPDGYLTLTDRAKDVIKSGGEWISSVELENALMAHPAVAEAAVVAVPDDKWGERPLATVVLKEGATADFAALRAFLADEGKIAKWQLPERWTVIESVPKTSVGKFDKKVLRRQYAEGHLDVTRL
>NZ_LN831790.1|WP_029384325.1|4362497_4363058_+|SigE-family-RNA-polymerase-sigma-factor
MTTPVCTSASEAAAAATQTLSYPSFASYVRARQPVLLRTARSLTANPSDAEDLLQTALTKTYVAWERIEDHRALDGYVRRALLNTRTSQWRKRKVDEFACDELPEPEPAPGGDDPAERQALRDAMWRAVMRLPARQRAMVVLRYYEDLSEAQTAAVLGVSVGTVKSAVSRALGKLRDDPELRVSGP
>NZ_LN831790.1|WP_029385458.1|4377194_4377935_+|response-regulator-transcription-factor
MTTTSPQGRTELLRPDGSPVRVLVVDDELSITELLSMALRYEGWQIRTAGDGHGAIRTAREFRPDAVVLDMMLPDMDGLAVLGRLRRELPDVPVLFLTAKDAVEDRIAGLTAGGDDYVTKPFSLEEVVARLRGLIRRSGAADRRADSVLVVGDLTLDEDSHEVTRGGDSIHLTATEFELLRFLMRNPRRVLSKAQILDRVWSYDFGGQANVVELYISYLRRKIDAGREPMIHTRRGAGYLIKPAVS
>NZ_LN831790.1|WP_029385457.1|4377931_4379506_+|HAMP-domain-containing-histidine-kinase
MTDRRRPGPRRRAGTPRTLRTRLVVAAVVLIAVVCAVIGTVTTLALRSHLYDQLGGQLEEVAGRASGNFGPPGGMEGGATPPGQQGKRIVLTEFVTKGPQPGGTVAARIEDGTVTEATVGKQSTDYQFGAEALTEAQTEALAAVARDGRPHTVDLPGLGGYLARYAQGVNGAFYVAVPTTQVDSTLNTLVLIEVSVTVAGLVAASLAGTVIVGLATRPLRRVADTATRVAELPLHAGEVNLDERVPESECDPHTEVGRVGAALNRMLDHVHGALHARQQSEMRVRQFVADASHELRTPLASIRGYAELTRRGREQVGPDTRHALGRIESEAGRMTLLVEDLLLLARLDAGRPLRFEQTDLVPLVVDTVSDARAAGPDHTWRLDLPDEPALARADPARLQQVLVNLLANARTHTPPGTTVTARVRHHGGWLCADVEDDGPGIPPGLLPHVFERFARGDSARSRATGSTGLGLAIVQAVTAAHGGAVTVDSVPGRTVFTVYLPAPGPRPVGSQAHHSLTTRVGQGG
>NZ_LN831790.1|WP_029385456.1|4379520_4380813_+|bifunctional-glycosyltransferase-family-2/GtrA-family-protein
MRTDSSPGTLPAREHLPAAAAGTPVLDVVIPVYNEEKDLGPCVRRLHEHLVRTFPYGFRITIADNASTDTTPRVAARLAEQIAQVRSVRLEQKGRGRALRAVWSASDAPVLAYMDVDLSTDLNALLPLVAPLISGHSDLAIGSRLSRSSRVVRGAKREFISRTYNLILRGSLQARFSDAQCGFKAIRRDVAQVLLPLVEDTGWFFDTEMLVLAERAGLRIHEVPVDWVDDPDSTVHIVKTATEDLKGVWRVGKALATGALPLDRLARPFGDDPRDRNIGDVPRGLARQLVGFCVVGVLSTLFYLLLYSGFRLVTGSQAANALALLVSAVANTAANRRLTFGVRGRGGAVRHQAQGLVVFAIGLVLTSGSLAALNAASADPAHSTELAVLIAANLAATVLRFLLFRAWVFPDAPPAPYEPHRFPTDPRDAR
>NZ_LN831790.1|WP_047121917.1|4380809_4382969_+|glycosyltransferase-family-39-protein
MTTPDTPALLPGLAPADPPAPPPAPAAGRASLPRRLWRGRPEDPRWVRPAFLGLLLATGLLYLYGLSASGYANSFYSAAAQAGSRSWKAFFFGSLDAANAITVDKPPAALWPMALSVRLFGLNSWALLVPQVLMGVGTVAVVYAAVRRRSGPGAGLLAGVVLALTPVAALMFRFNNPDALLALLMSVACYLVVRALEDGRTKWLVWAGTAIGLAFLTKTLQAFLVLPALALAYGVCAPVRPRRRLVQLASATAALVVSGGWWVAIVELWPAASRPYIGGSQTNSFLELTFGYNGLGRLNGEETGSVGGGGGAGGGQWGETGWDRMFNAEVGGQIAWLLPAALILLAAGLVLTRRLPRTDPARGAFLVWGGSLLTTMAVFSYMAGIFHQYYTVALAPYLAAVVGMGAAALWERRASAGASLTLAAALTATAAWGYVLLLRTPDYLPWLRWLVLVGGLAAALGLVFAGRLGRRTALAVAAAALVAALAAPAAYTVSTVREGHSGSIVTAGPAGASMRGGGPGGARGGGFPGGGMPGQGQGQGQGGGDGQGRNQPGGGLPGGGLPGGGPAGGGLPGGTLPGGGTAGEGGRTGGGAGGMGGLLDGAQVGSEARELLETGADRYTWAAAAVGSQNAASYQLATGEPVMAIGGFNGTDPSPTLAQFRQYVADGRIHYFIGGGTGGRMGGDSGSSAQIASWVEARFEKVTVGSATFYDLTCPTSTG
>NZ_LN831790.1|WP_029384495.1|4383066_4384581_+|MFS-transporter
MTTPPQEHAREEPGRAPRTQPQGHPQRWLILGVICLAQLTVVIDNTVLNVAIPSLTREMDAATSDIQWMINAYSLVQSGLLLTAGNAADRYGRKKMLFAGLALFGLGSLVAGLASSTGQLIAARAGMGIGGALLLTTTLAVAMQIFTPEEQPRAIGVWAAVNSLGFAAGPLLGGLMLNHFWWGAIFLINLPVAALGLVAVVTLVPESKNPQGDRPDLLGALLSTIGMASLVFAIISGPGHGWASQRVLASAAVAVAALGAFAYWESRIPYPMLDLHFFRNRRFTGAVAGAVLITFGMTGAMYLLTQHLQFVLGYDALEAGLRTSPLALTFVALNFTGLTAKWTARMGLPVSIALGMTLTAAGLAAIALLASGGYAGTLLGLLLIGVGCAIASPAMAHAIMSSIPREKAGVGAGINGTLAEFGNGLGVAVLGAVLNARFAALVSVTASSLPAALASAGSAAERERITDAFSAGLESSQLVGAVAVLLGGLVAAVLLRRAERAEAS
>NZ_LN831790.1|WP_029384494.1|4384697_4385453_+|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein
MAEAAHGVRETSVWLKDKARRGGRGGGQPGLDRDRVTEAAVRLLDAEGLARFSMRRLAAELNVTPMSVYWYVDTKDDLLELALDAVMGEFRLPDAAAGEDWRDQLRALAREYRGLLVRHPWVSPLAGTFLNIGPNYLAFSRTVQRVVRRTGVPEHRVTSVISAVFQFVYGYGTLEGHFLAGAAASGLGPDDYFRHAMTAVSDVPQAAEVIEESKKIMAARGGGTVAEMMERDFEYALDLLTAGIEVMVARG
>NZ_LN831790.1|WP_029384492.1|4385500_4385971_-|PPOX-class-F420-dependent-oxidoreductase
MAPNIATNTRVSLDELLDFIRPRHRAILLTRRADGSPQGSPLTCGVDDSGRIVVSTYPERAKTRNARRDQRVSLIVLSDDWNGPWVQIDGAAEVIDAPDSVEPLVEYYRNIAGEHPDWDEYRQAMVRQGKSIIRITPERWGPVATGGFPARLADGA
>NZ_LN831790.1|WP_029384491.1|4386027_4386381_-|STAS-domain-containing-protein
MTFLPNPTEPSPPPGCALLALPPEIDYCNADAVLSLVLSAVGGHGRGLRLLVLDLTGTRFMDSQGVRLVNDVRQRLHPRARVRVVARPGGVASRVLELTGLRRDVPVYDNVAEAMAS
>NZ_LN831790.1|WP_029384490.1|4386590_4387361_+|ANTAR-domain-containing-protein
MPKRFVVTASEFGDLPRFPGGSGGFELAEALTAAARRLHETDTPHTTLSTAVRLAVRFMPGAEHAGISVIERGSRPYTSQRRPLAWTDEVVRSVESRHGGREPHPHWEHLWTQPVARIEDSEADGGGGVLSAAGLRSALALRLRADRRRLTVLTAYASKPRAFGEDATRIGRLFTAHVGIALDSATVREQLTEAMRTRDLIGQATGILMERQNIDAASAFESLVKASQRENVKLRDLARRIVDTHGTTAGRGVNER
>NZ_LN831790.1|WP_029384488.1|4387379_4388081_+|GAF-and-ANTAR-domain-containing-protein
MRPETPETLDQAMVRSQGLDTLLRDLTDRAVQEVPGAAACSLTVRRADRLMTLAGSSGLPSGLDLRQYENGSGPCVDAAETGTAQYAADLAVESRWPPYTAYALAAGVRCVLALPLPVEGERGAAINFYGVEPGALGEGVPAARAFAERATDAVDTALRIERQRQSAVDVRTALLSRSVIDQAIGILMARERVDARIALERLRRASQDSNVKLRDLCSDLVARTARGGSGGRQ

Crispr_ID: NZ_LN831790_8

• CRISPR_ID: NZ_LN831790_8
• CRISPR_location: 4463841-4463926
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_8

Consensus_repeat	Method
GTGGGCGGCTGTGGGGCCGTGGGGGTGCG	CRISPRCasFinder

spacers of NZ_LN831790_8

>8.1|4463870|28|NZ_LN831790|CRISPRCasFinder
GGCATCTCCGGGCACGTCCCTTCTCGCT

CRISPR arrays and Neighbor proteins around NZ_LN831790_8

CRISPR arrays

The CRISPR arrays of NZ_LN831790_8

>merge|NZ_LN831790|8|4463841-4463926|CRISPRCasFinder
GTGGGCGGCTGTGGGGCCGTGGGGGTGCGGGCATCTCCGGGCACGTCCCTTCTCGCTGTGGGCGGCTGTGGGGCCGTGGGGGTGCG

>NZ_LN831790|8|8|4463841-4463926|CRISPRCasFinder
GTGGGCGGCTGTGGGGCCGTGGGGGTGCG	GGCATCTCCGGGCACGTCCCTTCTCGCT
GTGGGCGGCTGTGGGGCCGTGGGGGTGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047121923.1|4454809_4456219_-|PrsW-family-intramembrane-metalloprotease	unknown	unknown	gnl|CDD|379143
NZ_LN831790.1|WP_029383924.1|4452669_4453707_+|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_LN831790.1|WP_079025155.1|4457585_4458830_-|L-2-hydroxyglutarate-oxidase	unknown	unknown	gnl|CDD|183292
NZ_LN831790.1|WP_029385569.1|4467195_4468575_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224172
NZ_LN831790.1|WP_029383925.1|4453815_4454760_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381307
NZ_LN831790.1|WP_162183955.1|4451088_4452234_+|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl|CDD|369272
NZ_LN831790.1|WP_029382167.1|4478283_4478958_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_LN831790.1|WP_176572919.1|4465986_4466736_-|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_LN831790.1|WP_029382170.1|4480930_4482478_-|type-VI-secretion-protein	unknown	unknown	gnl|CDD|237865
NZ_LN831790.1|WP_029386310.1|4458876_4460301_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_099053657.1|4478954_4480331_-|two-component-sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_LN831790.1|WP_047121925.1|4463955_4465761_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|214816
NZ_LN831790.1|WP_029383927.1|4456270_4457149_-|tRNA-(guanosine(46)-N7)-methyltransferase-TrmB	unknown	unknown	gnl|CDD|234649
NZ_LN831790.1|WP_029382169.1|4480329_4480911_+|N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831790.1|WP_029386309.1|4461151_4463347_+|asparagine-synthase	unknown	unknown	gnl|CDD|223444
NZ_LN831790.1|WP_029381839.1|4470407_4471682_-|MFS-transporter	unknown	unknown	gnl|CDD|340887
NZ_LN831790.1|WP_029383921.1|4449556_4450687_+|dihydrofolate-reductase-family-protein	unknown	unknown	gnl|CDD|180169
NZ_LN831790.1|WP_029381840.1|4471852_4472401_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831790.1|WP_047121927.1|4468747_4470388_+|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl|CDD|369272
NZ_LN831790.1|WP_029383919.1|4447757_4449293_+|amino-acid-permease	unknown	unknown	gnl|CDD|273331

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047121923.1|4454809_4456219_-|PrsW-family-intramembrane-metalloprotease	gnl|CDD|379143	pfam13367, PrsW-protease, Protease prsW family. This is a family of putative peptidases, possibly belonging to the MEROPS M79 family. PrsW, appears to be a member of a widespread family of membrane proteins that includes at least one previously known protease. PrsW appears to be responsible for Site-1 cleavage of the RsiW anti-sigma factor, the cognate anti-sigma factor, and it senses antimicrobial peptides that damage the cell membrane and other agents that cause cell envelope stress, The three acidic residues, E75, E76 and E95 in Aflv_1074, appear to be crucial since their mutation to alanine renders the protein inactive. Based on predictions of the bioinformatics programme TMHMM it is likely that these residues are located on the extracytoplasmic face of PrsW placing them in a position to act as a sensor for cell envelope stress.	2.40977e-56
NZ_LN831790.1|WP_029383924.1|4452669_4453707_+|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	1.88872e-34
NZ_LN831790.1|WP_079025155.1|4457585_4458830_-|L-2-hydroxyglutarate-oxidase	gnl|CDD|183292	PRK11728, PRK11728, L-2-hydroxyglutarate oxidase.	0
NZ_LN831790.1|WP_029385569.1|4467195_4468575_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	2.49497e-99
NZ_LN831790.1|WP_029383925.1|4453815_4454760_+|aldo/keto-reductase	gnl|CDD|381307	cd19081, AKR_AKR9C1, AKR9C family of aldo-keto reductase (AKR). Haloferax volcanii aldo-keto reductase is a founding member of aldo-keto reductase family 9 member C1 (AKR9C1).	1.5342e-164
NZ_LN831790.1|WP_162183955.1|4451088_4452234_+|SpoIIE-family-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	2.03158e-42
NZ_LN831790.1|WP_029382167.1|4478283_4478958_-|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	7.55025e-70
NZ_LN831790.1|WP_176572919.1|4465986_4466736_-|TetR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	1.00001e-09
NZ_LN831790.1|WP_029382170.1|4480930_4482478_-|type-VI-secretion-protein	gnl|CDD|237865	PRK14951, PRK14951, DNA polymerase III subunits gamma and tau; Provisional.	1.57424e-06
NZ_LN831790.1|WP_047121927.1|4468747_4470388_+|SpoIIE-family-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	3.32772e-50
NZ_LN831790.1|WP_099053657.1|4478954_4480331_-|two-component-sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	5.07066e-36
NZ_LN831790.1|WP_047121925.1|4463955_4465761_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|214816	smart00776, NPCBM, This novel putative carbohydrate binding module (NPCBM) domain is found at the N-terminus of glycosyl hydrolase family 98 proteins.	2.58453e-41
NZ_LN831790.1|WP_029383927.1|4456270_4457149_-|tRNA-(guanosine(46)-N7)-methyltransferase-TrmB	gnl|CDD|234649	PRK00121, trmB, tRNA (guanine-N(7)-)-methyltransferase; Reviewed.	3.70954e-95
NZ_LN831790.1|WP_029382169.1|4480329_4480911_+|N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	5.16498e-11
NZ_LN831790.1|WP_029386309.1|4461151_4463347_+|asparagine-synthase	gnl|CDD|223444	COG0367, AsnB, Asparagine synthase (glutamine-hydrolyzing) [Amino acid transport and metabolism].	5.85116e-06
NZ_LN831790.1|WP_029381839.1|4470407_4471682_-|MFS-transporter	gnl|CDD|340887	cd17329, MFS_MdtH_MDR_like, Multidrug resistance protein MdtH and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of Escherichia coli MdtH and similar multidrug resistance (MDR) transporters from bacteria and archaea, many of which remain uncharacterized. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. MdtH confers resistance to norfloxacin and enoxacin. MdtH-like MDR transporters belong 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.	4.63503e-67
NZ_LN831790.1|WP_029383921.1|4449556_4450687_+|dihydrofolate-reductase-family-protein	gnl|CDD|180169	PRK05625, PRK05625, 5-amino-6-(5-phosphoribosylamino)uracil reductase; Validated.	2.20408e-44
NZ_LN831790.1|WP_029381840.1|4471852_4472401_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	3.62442e-18
NZ_LN831790.1|WP_029383919.1|4447757_4449293_+|amino-acid-permease	gnl|CDD|273331	TIGR00907, Choline_transport_protein, amino acid permease (GABA permease). [Transport and binding proteins, Amino acids, peptides and amines].	1.00514e-134

Protein sequences

>NZ_LN831790.1|WP_029386309.1|4461151_4463347_+|asparagine-synthase
MRWLVGWSSTAAGAVGAGTAGATGYDGETVQPVGSQLLWGDPDPLWAVGDWRPDEVRVVHADAQTRIAVLGICGATDEQLRVALFTARGGALRHLTAWPGSYTAVVQVGRRITVCGDLAGARPVFHTPWAGGTAYATAALPLADLVEANLDFGYLAALLAAPDVPAALDDATPYDGVKRVPPGHALILRAGAREVAGYEPVASLAVAAPPADPDSAVDGVREALVEAVRTRLAAPRHVPGFPGDGIDPGPVPGMGPADRRAARGMPAPGIGADLSGGPASGTLALLAAGLPGRPGTVLGHGGTGAGERLLAVTFNDLAVGGPEAELERAGALAAGPRLHHVVVTGGEETLPYADLDGPLTDEPGPCLVSAARHRARLAAGSADHFTGYGARQVLDAHPARLADLLMDRKRRHLVRPVAALARADGSVLVPARVYAAARRLARTPYRAGLEDLAERLLRRRFDETGGGAGRVGRTGRTGRAGWPGGDAGADGAGGAVEASLAALTWGRPGPAARWLTGEALAEVSVRLQASTHRSGLGPGQRPGDFRARAALARQAAEVRVLEQAAEIRFQRLHAPFLDNQVVRACRALPEALRVRPGARAAILRTVLEGAGVSGLPPGWGAPTQAVATAAARTGLRVAADSLVALFDTPLLAEAGLVEARVVRKALRGAAAGEPLPLDGLADLVSLELWLRRLLARRGTCWTGTPGRQRAVPGGIAPQRGVLGASAVVRRA
>NZ_LN831790.1|WP_029386310.1|4458876_4460301_-|hypothetical-protein
MSREQRGPNEKLGAVLALAGISNAGLARRVNDLGAQRGLTLRYDKTSVARWVSKGMVPQGAAPHLIAAAIGQKLGRPVPLHEIGLADADPAPEVGLAFPRDVGQAVKSATELYRLDLAGRRAGSGGIWQSLAGSFAVSAYATPASRWLITPADSSVAREASPGEGSAAPLKVGHSDVQKLREAAEDARRWDSKYGGGDWRSSMVPECLRVEAAPLLLGSYSDEVGRALFGAAAELTRLAGWMAFDTGQQEAAQRYYIQALRLARAAADVPLGGYVLASMSLQATYRGFGDEGVDLAQAALERNRGLATARTMSFFRLVEARAHARAGDAQAAGAALRAAESWLERARPGDHDPTWLGFYSYDRFAADAAECYRDLKAPRQVRRFTEQALSRPTEEYVRSHGLRLVVSAVAELESGNLDAACEQGVRAVEVAGRISSARTTEYVKDLLHRLEPYGDEPRVVELRERARPLLTTPA
>NZ_LN831790.1|WP_079025155.1|4457585_4458830_-|L-2-hydroxyglutarate-oxidase
MHYRTREVEQVEREKIAYDCDVLVIGGGIVGLSTAYAISRAAPGTRVTVLEKEPGPARHQTGRNSGVVHSGIYYRPGSLKARYAVRGAAEMVKFCAEYGIAHAVTGKLIVATDRVELPRLHALVQRGRENGIPVRELGAAQITEYEPEVRGLAAIHVGTTGICDYVAVARQLAAASGARIRYGAQVLRIDRRPSRGVAALTRSGDIVRARVLVNCAGLYCDEVARMAGDDPGMRIVPFRGEYYELARPELVRGLVYPVPDPAFPFLGVHLTRGIDGGVHIGPNAVPALAREGYGWSTVRPRELASTLTWPGSWHIARRHWRYGAGELRRSLSKAAFTSAVRRLLPAVTEDDLVPTAAGVRAQAVLPDGTLVDDFLIREGARTVHVLNAPSPAATASLPIGREVARRALTALAGT
>NZ_LN831790.1|WP_029383927.1|4456270_4457149_-|tRNA-(guanosine(46)-N7)-methyltransferase-TrmB
MSDSRNAPEAPQHPAPSPLGDGGALRHARAKGEPRFPEGPKADPAGSHFERRIRSFQPRRSRVTAGQADALQRLWPKWGFDIDGRRVLDPAELFGNTNPVVLEIGFGMGEATAQMAAADPDTNILAVDVHTPGQGNLLNLADRGGLSNIRVGNGDAIILLREMLRPDSLDGLRVYFPDPWPKKRHHKRRLIQPEFLTLAATRLKPGAIVHCATDWEPYAEQMLEVLTAHPDYENTQPDGGFAPRPAHRPLTRFEGQGLDKGHVVNDLLFRRVPRRPQPEPADQHRLQPPTGA
>NZ_LN831790.1|WP_047121923.1|4454809_4456219_-|PrsW-family-intramembrane-metalloprotease
MATSPPHPTTYPTRPPSGPPAGPLRHTHPHWWQRPWVRYGALITLLALSGLVILALVREETGTQGFLVGLGLAVLPVPLLLAAFRWLDRVQPGPWRNLLFSFAWGACAAALIAIVANSFATQWIATATADPDGADTLGATVIAPVVEESAKAAAVLLVFLFRRRDFTGIVDGVVIAGVTATGFAFTENILYLGTAFGTDQLTGDTGIASVTAATFFVRIVMSPFAHPLFTVLTGIGFGLAALRPDRRAALRVLLPLAGLLLAMGMHALWNGSSTLGDLGFLAVYAAFMVPAFGLLTWLVIWTRQRELRTVRTELPPYVAAGWLSPSEPYALGSMRARRIARQYARRYGGKPAARAVMRYEAYATSLAFLRHRARHGRAGADFAARERELLGELWNRHEPARPALEHAARITAPPPVMPPPMPWAPYGPAAARPPHPQAPYAAPAPYQPQPQPQPHPQPQPYYGYNPYRS
>NZ_LN831790.1|WP_029383925.1|4453815_4454760_+|aldo/keto-reductase
MTSLRKLGYSDLEVFPLSLGGNVFGWTADEAASFAVLDAYTAAGGNFVDTADSYSAWVDGNSGGESETIIGKWLKARGNRADVVIATKVSQHPEYQGLSAANIKAAADASLRRLGTDHIDLYYTHFDKPEVPVEEILGALDELVRVGKVRYIATSNISAERLRASLEFSEREGLARYVALQPHYNLVSRDTYEGELQDVAERAGLAAVPYFALAAGFLTGKYRPGTTVDSARAEGAARHLGSERGQRVLTALDEIAQAHGAPVATVALAWLAAQPTVAAPIASARTVEQLPALLGVAELTLTPEELDRLTQASA
>NZ_LN831790.1|WP_029383924.1|4452669_4453707_+|M23-family-metallopeptidase
MASNRPAPEAPFVPSPRDTDVFGHGGPLPGEGPFEEWNPTAESVRPVRGRHRVAKQRGGLARSSTVLGVGVIAAVGAGGMASAQAGKSPVPISMPDLPSVGSLVANDEEQSAPEVSAAPLSSAGMTSSDTAQGAADAGEALRARIMAQAEQQQDQVESKAVADAAAAAEKEAARAAAEAAKEAEAKAAAEKAKAEEEARKKAEAERLAELARQYALPTSSYTLTSTFGQAGPYWSSGHHTGLDFAAPTGTLIKAVHSGTITSAGWDGSYGYKTVLTLEDGTEIWYAHQSSISVSVGQKVATGDVIGRVGSTGNVTGAHLHLEVHPAGSGSGVDPAAWLRSKGLTL
>NZ_LN831790.1|WP_162183955.1|4451088_4452234_+|SpoIIE-family-protein-phosphatase
MVRPGDVEEEPYARVPAPAGGGAGRPGSRLQTLVRLLPALLLVVGVLYDCLSPRNFTAAPLFAAAPLVAAPLFSRRGTLLTGLASVAAVFGVHLAFGALARVDAITELVTVATVAALAVLINGLVRRTGERLASAREIAEAAQRAVLPEPAERIGGFEIAACYEAAQADAFIGGDLYAVQDSPHGLRLVVGDVRGKGMGAVAAVAVVIGAFREAAEQEATLEAVARRLERALAREGTRREGLDAFEGFTTAVLAELPHGDGIVRIVNRGHPPPLLLYADGSLRTLLPTREYSLPLGMGELGVWPDRAEEVVLPGGATLLFYTDGLTEARDSHGEFYDPGVRLAGRTFPRPAELLAALADEVRRHSGGGMADDMALLAVRRP
>NZ_LN831790.1|WP_029383921.1|4449556_4450687_+|dihydrofolate-reductase-family-protein
MPLPYVLLSAAVSLDGYLDDTGPERLLLSGPEDFDRVDGERASADAILVGAGTIRADNPRLLVNSAERRAARIAAGKPEFPLKVAVSGSGELDPAAPFWHTGGDKVLCTTERGAVRARALGIAADVVAFGAELDWRAVLSYLHDERGVRRLMVEGGGSVHTQLLRRRLADELQLALAPLLVGDPDAPRLFGPGAYEDGRLRLVETRRLGDVVLMRYQPTAPGTGATVSAADRHWLALACDLAAQCPPSETAFSVGAVVVAADGTELARGHSREGGDAVVHAEEAALAKTDPADPRLATATVYSSLEPCARRASRPAPCARLILDAGVRRVVTAWREPDTFVPGADGSGVLAAGGAAVLFLPELQARAKAPNRHLTG
>NZ_LN831790.1|WP_029383919.1|4447757_4449293_+|amino-acid-permease
MTDDAKASGLSDEERLAQLGYTQVLARRMSAFSNYAVSFTIISVLSGCLTLYLFGMNTGGPAVITWGWVVVGLMTLFVGLAMAEICSAYPTSAGLYFWAHRLAPARSAAAWAWFTGWFNVLGQVAVTAGIDFGAASFLGAYLNLQFGFEVTPGRTILLFAAILLLHGLLNTFGVRVVGLLNSVSVWWHVLGVAVIAGALALVPDRHQPASFVFGEFVNNTGWGSGAYVVLLGLLMAQYTFTGYDASAHMTEETRDASTAGPKGIVRSIWTSWAAGFVLLLGFTFAIQSYEGALTSPTGAPPAQILLDALGATAGKLLLLVVIGAQLFCGMASVTANSRMIYAFSRDGALPFSRLWRTVSPRTRTPVAAVWLAAGGALALGLPYLINVTAYAAVTSIAVIGLYLAYVIPTLLRVRKGAAFQRGPWHLGRWSQAVGVVAVAWVGFITVLFMLPQVSPVTWETFNYAPVAVLVVLGFAAVWWRVSARHWFLVPGRAGDRAGEGTAAAPAEPVDP
>NZ_LN831790.1|WP_047121925.1|4463955_4465761_-|sigma-70-family-RNA-polymerase-sigma-factor
MSVDERDGSLGDGDGDAEAGGPPHVPAPADDRGATGRAEEDGVLPPSDAELIGWMRSGDDTAYEELFRRHAGAVRRYARTCCRDPHTAEDLTAEVFARMLQAVRGGFGPEHAVRAYLLTSVRRVAAGWTQSAKREQLVDDFAVFAAQAARLSEAPEDAVELGADVRAMHEAEQSLAMRAFRSLPERWQAVLWHTEVEDESPSEVATLFGLDAGGARVLASRAREGLRQAYLQAHVSSALTDDEECARYADRLGSYARGRLRTRAERGLRKHLEECARCRLAAGQIQEVAGGIPALVPVAVIGWFGTAGYGKVAGLLAGGAAAAGGGASGTTPASPGLGAPVKAGVTTGVVAVGAVAAVVLALAGNDTPAEPEPKAAPRPSSPPAQPREQPPTPPQPPPTRIPPPTPAPPPPAPAPTLTPTTPRPTPTPTPTPTPIRTPTPTPTATPTPTPTATPPPAPTTYAWSELPYDADGDGSGPEMRLGESGWLWQRHGLSIAGRQYAHGVTVRGSSSVTIDLNRACSAYDALVGVDDLTAKLGKVHFSVHADGTQLWDSGKIKGSDPAVPVHVDLTGRETVRLVVEPHSPVDNAALADWAESKFTCA
>NZ_LN831790.1|WP_176572919.1|4465986_4466736_-|TetR-family-transcriptional-regulator
MSSVPSGAAVTAAGMAGAGRGDAARTTPLRVDAQRNLEHVLRAAREVFGELGYGAPMEDVARRARVGVGTVYRRFPSKDVLVRRIAEEETSRLTDQARAALRQEDEPWSALSRFLRTSVASGAGRLLPPQVLQVGVADESGDDAGEPRVPQQRMQPGPGELRLVSGERTAAAGPVPAEHDAGAAALLEVVGQLVERARAAGELRPDVSVSDILLVIATAAPSLPDAAQRAAASARLLDILLEGLRSRPA
>NZ_LN831790.1|WP_029385569.1|4467195_4468575_+|NAD(P)/FAD-dependent-oxidoreductase
MVKERARILVVGGGYVGMYTALRLQRKLKGELRRGEAEITVVTPDPYMTYQPFLPEAAAGSLSPRHVVVPLRRVLDRCRVLIGEATAVDHAARTATVTTLATEEEGTGARRLTYDELVLAPGSVARTLPVPGLAEHGIGFKTVEEAIGLRNHVIEQMDIASSTRDPALRDAALTFVFVGGGYAGVEALGELEDMARQAARSYHNVGRDDMKWVLVEAAGRVLPEVGEELGRHTVTELRRRNIDVRLRTRLESCADRVAVLSDGTRFPTRTVVWTAGVKPHPLLAATDLPRTPRGRLKCTPELRVEGAPHAWAAGDAAAVPDVTADAPGAECAPNAQHAVRQARVLGDNIAHALRGEPLTTYAHRHAGSVASLGFHQGVAHVRGRKLKGFPAWVLHRAYHLSRMPTANRKARVLAEWTLSGFFAREIVSLGSLEHPRVEFELAAGGNPPEEPPRNPKGSS
>NZ_LN831790.1|WP_047121927.1|4468747_4470388_+|SpoIIE-family-protein-phosphatase
MDFTRWSVRLPRTQRRTAARAGTTVSPDRRGEGSVPAARAGQPGDGAPPVPAVDDLPAREVLDRVPALVALLHGPDHRIAYVNGAYTAAFGARPLGEPAREALLELDELGLFPLLDQVQRSGRPRTVKSRKAPDGRSYTFTCTPVTEGDTGGVLVFATDVTDHAEAAARLRASERRQRETAVTLQHSLLPQKLEQPDDLRIAATYHPGGTEAAVGGDWYDVITLGGGRTALVIGDVMGRGVRAAAVMGQLRTAVRAYARLDLPPHEILQLLDGLATEIDANQIATCVYAIHDPNEGRLVYASAGHLPILVRDDNGTVLRADEPTGPPLGTGGWIHASGSVPLTPGSTAVLYTDGLVERRDEDLDEGIAALERALAGATGTPQVVCDRLVRSAGVTADHDDDVAVLVLQHPARTGPEGELFRNAALELLGGVEAAPRARAFASGVLTSWRFPTDLHDLGVLAASELVANSLQHGTPPMRLRLRRTDRRLIVEVTDGDDHLPRRRRAEPGDETGRGIAIIATIASNWGSRRTPGGGKAVWCEFALPTR
>NZ_LN831790.1|WP_029381839.1|4470407_4471682_-|MFS-transporter
MGAAMRRIHVGNALSAFGLGFTVPYLYVYVAQVRGLGSVTAGLVLAVFAVAALIVLPFAGRAIVRRGPLPVLLVALVTAAVGALSLGLASSAAAVLLSAAALGAGQAVMQPALATMIVDCSSTETRSRAFAMQFFLQNLGLGVGGLIGGHLVDTSSASSFTLLFAIEAAMFLLLVAVMATVRTPRAPRVEDAPGQSGQGSWKQLLGNRAMVQLCVLGFVLFFACYGQFESGLSAYGVEAAGISTSVLGTALAANTLMIVVAQFAVLKFVERRKRSRVIAAVGLIWAVAWAVAGYAGLGHGSQAMATAAFISTYALFGLGEAMLSPTLAPLVADLAPTGMAGQYNSAFALVKQLALAIGPAVGGPLGASLHAPYIVAFLLFSLGITVLALRLGRQLTEAQDQPWAARSRVVSRGGSAAEAVPADA
>NZ_LN831790.1|WP_029381840.1|4471852_4472401_+|MarR-family-transcriptional-regulator
MGDTSGVSEPTLEEQIAAYQREFQDLDPQVEKIVSALSRLNRRMNVAYGRQTAALGISNAEWEVLKALVLSGAPYRMGPGDLAKRLGLTPAAMTHRIDRMVTEGLVTRERDESNRVRVIVELTHDGREKWLEAMRLATVFEEDLLQDLSPEERTALGEVLTRLLRRVEHAQPDAGGRLSDLD
>NZ_LN831790.1|WP_029382167.1|4478283_4478958_-|response-regulator-transcription-factor
MTTVLIADDQPLQRLGFRMLLESQDDLTVLAEASNGSEAVRLAADHHPDVVLMDVRMPGLDGIEATRRITATGDRTRILILTTFDLDEYAYAGLRAGASGFLVKDAQPEELLSGIRAVATGDAVVAPSLTRRLLDAYVHHLPAGPAEGPDAVDTDPRLAALTDREREILTVIGQGWTNTEIAERLHLAESTVKTHVSRVLAKTGSRDRVQAVILAYDTRLVTPS
>NZ_LN831790.1|WP_099053657.1|4478954_4480331_-|two-component-sensor-histidine-kinase
MRATVVLRYYGPHLISAPRSDAPGAGVRQHGGMRSEFRTTEAGSTMGPVTEQRPAEPLTEHVHRLTRRLRAFDRRHPLLWDAHFTGFWVLAALVDYYGGGWRTTAHDLDVPGGLLLALSLGFSVPLLGRRSHPRAVLLVMAPVAFVNAWSGAALQASLLQLVVLYHVALRLPLRALWWAAPLLTAPVVVSAVRYGEGTWHQQVGSHLTSILVAALIGVTVRTRRSYTDALEDRARRLEIERDQQVLLAAAAERARIAREMHDIIGHNLSVITGLADGGRYAAAKSPQRAAQALDAIGTTSRQALSELRRLLDVLREEEKEEAALTPQPGLTDLDRLLAGVRDAGLPVRTTVHGRPALPPGRQLTVYRVVQEALTNTLKHAGPGATSEIDLSYGEGGAVTVVITDTGPGWPAPASSDGRGLPGMRERTALYGGTLEAGPRPYPERGWRVCLHLPEEAPQ
>NZ_LN831790.1|WP_029382169.1|4480329_4480911_+|N-acetyltransferase
MSAPVSGDWVIRAVRADEWAAVRALRLAALRDPVARIAFLESYEAAADRPESFWRERAAGAAEGAAGARQVVAEVPGGAWAGTLTVLIEEAGTTDWAGLPVERRQGHVVGVYVRPEWRGTGLTGALFDAGLAWAWRRGAERVRLIVHEDNGRAQGCYRKLGFVPSGVSVPMQGAPEERELEFELGRDRLAGPA
>NZ_LN831790.1|WP_029382170.1|4480930_4482478_-|type-VI-secretion-protein
MRRDDHHREQGGIPDGLLLGILAFLLGMTLLAWTATGLAGLFAHGSWPRGVTFARTPLAMRHLVAQPHDLPGAWPDAPASQLSGYGLFWGLFIGQLMVLLVLTVFVMGTLARWRAVRLRRRTEQATPAPGPARGPESAVPAPTALQGQPPAPQAPPAPSPAARQEIPAPAPPEFPTPRTAPERPQPLAATAPGAPPPTPSFGGEQPGRWERVFLGTRESRRATAGQAVLDAAGPALVVTSDPALWQATKDARAKLGPVLLYDPTHLCDTPARLHWAPTTGCEDRPTATARAAALLTPVRPTARLDQAVGDTAEVLLRSYLHAAAVDGRTIRHVHRWAQGTQIQDAVRVLRTNPKAAPGAAGELEAALTAHPERREMAQQLTTRALSALFTVNVRESCTAHRTDALALGSFVHEGGTLYVVGESIEDPRTDPGAMPLLTALVASVVEHGRRMAERSSSGRLDPPLTLVLEDVAAVAPLSHLPELLATGADRGLPTLALLRSREQGRARWPDAELPV

Crispr_ID: NZ_LN831790_9

• CRISPR_ID: NZ_LN831790_9
• CRISPR_location: 4714180-4714313
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_9

Consensus_repeat	Method
GGCTCCCCCTCCGCGCCGCCGCGGCCGATCCCCGCTGG	CRISPRCasFinder

spacers of NZ_LN831790_9

>9.1|4714218|58|NZ_LN831790|CRISPRCasFinder
GACGAGGTCTACTTGCCGTCCCGGGTCAGGTCCGCCCCGGACATGCCTCGGCCGCGGT

CRISPR arrays and Neighbor proteins around NZ_LN831790_9

CRISPR arrays

The CRISPR arrays of NZ_LN831790_9

>merge|NZ_LN831790|9|4714180-4714313|CRISPRCasFinder
GGCTCCCCCTCCGCGCCGCCGCGGCCGATCCCCGCTGGGACGAGGTCTACTTGCCGTCCCGGGTCAGGTCCGCCCCGGACATGCCTCGGCCGCGGTGGCTCCCCCTCCGCGCCACCGCGGCCGATCCCCGCTGG

>NZ_LN831790|9|9|4714180-4714313|CRISPRCasFinder
GGCTCCCCCTCCGCGCCGCCGCGGCCGATCCCCGCTGG	GACGAGGTCTACTTGCCGTCCCGGGTCAGGTCCGCCCCGGACATGCCTCGGCCGCGGT
GGCTCCCCCTCCGCGCCACCGCGGCCGATCCCCGCTGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047121950.1|4714726_4717678_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|276938
NZ_LN831790.1|WP_029382700.1|4714320_4714515_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_047121947.1|4704793_4705282_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_LN831790.1|WP_047121949.1|4711098_4713501_+|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl|CDD|270916
NZ_LN831790.1|WP_049976748.1|4725775_4726852_-|tyrosine-protein-phosphatase	unknown	unknown	gnl|CDD|379135
NZ_LN831790.1|WP_029386169.1|4703586_4704099_+|EF-hand-domain-containing-protein	unknown	unknown	gnl|CDD|227455
NZ_LN831790.1|WP_029382703.1|4718515_4720060_+|APC-family-permease	unknown	unknown	gnl|CDD|223605
NZ_LN831790.1|WP_029382706.1|4724632_4725190_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029382704.1|4720079_4721606_-|PHP-domain-containing-protein	unknown	unknown	gnl|CDD|213987
NZ_LN831790.1|WP_029382702.1|4717835_4718231_-|nitroreductase-family-deazaflavin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|281995
NZ_LN831790.1|WP_029382709.1|4727022_4727349_+|antibiotic-biosynthesis-monooxygenase	unknown	unknown	gnl|CDD|225209
NZ_LN831790.1|WP_029386175.1|4708514_4708967_+|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_LN831790.1|WP_029382699.1|4713557_4714151_+|hypothetical-protein	unknown	unknown	gnl|CDD|240430
NZ_LN831790.1|WP_029386172.1|4706478_4707144_-|pyridoxal-5'-phosphate-synthase	unknown	unknown	gnl|CDD|235555
NZ_LN831790.1|WP_029386173.1|4707207_4707633_-|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl|CDD|274679
NZ_LN831790.1|WP_029386176.1|4709199_4709835_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831790.1|WP_029382707.1|4725173_4725686_-|DUF2165-domain-containing-protein	unknown	unknown	gnl|CDD|370754
NZ_LN831790.1|WP_029382705.1|4721924_4724510_+|bifunctional-FO-biosynthesis-protein-CofGH	unknown	unknown	gnl|CDD|236422
NZ_LN831790.1|WP_029386171.1|4705871_4706474_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_LN831790.1|WP_029386174.1|4707805_4708432_-|LysE-family-translocator	unknown	unknown	gnl|CDD|224199

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047121950.1|4714726_4717678_-|tetratricopeptide-repeat-protein	gnl|CDD|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	1.80539e-42
NZ_LN831790.1|WP_047121947.1|4704793_4705282_+|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	2.3659e-20
NZ_LN831790.1|WP_047121949.1|4711098_4713501_+|PQQ-binding-like-beta-propeller-repeat-protein	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.63575e-75
NZ_LN831790.1|WP_049976748.1|4725775_4726852_-|tyrosine-protein-phosphatase	gnl|CDD|379135	pfam13350, Y_phosphatase3, Tyrosine phosphatase family. This family is closely related to the pfam00102 and pfam00782 families.	2.1519e-76
NZ_LN831790.1|WP_029386169.1|4703586_4704099_+|EF-hand-domain-containing-protein	gnl|CDD|227455	COG5126, FRQ1, Ca2+-binding protein (EF-Hand superfamily) [Signal transduction mechanisms / Cytoskeleton / Cell division and chromosome partitioning / General function prediction only].	2.33579e-06
NZ_LN831790.1|WP_029382703.1|4718515_4720060_+|APC-family-permease	gnl|CDD|223605	COG0531, PotE, Amino acid transporters [Amino acid transport and metabolism].	1.32491e-26
NZ_LN831790.1|WP_029382704.1|4720079_4721606_-|PHP-domain-containing-protein	gnl|CDD|213987	cd07432, PHP_HisPPase, Polymerase and Histidinol Phosphatase domain of Histidinol phosphate phosphatase. HisPPase catalyzes the eighth step of histidine biosynthesis, in which L-histidinol phosphate undergoes dephosphorylation to produce histidinol. HisPPase can be classified into two types: the bifunctional HisPPase found in proteobacteria that belongs to the DDDD superfamily and the monofunctional Bacillus subtilis type that is a member of the PHP family. The PHP (also called histidinol phosphatase-2/HIS2) domain is associated with several types of DNA polymerases, such as PolIIIA and family X DNA polymerases, stand alone histidinol phosphate phosphatases (HisPPases), and a number of uncharacterized protein families. The PHP domain has four conserved sequence motifs and contains an invariant histidine that is involved in metal ion coordination. The PHP domain of HisPPase is structurally homologous to other members of the PHP family that have a distorted (beta/alpha)7 barrel fold with a trinuclear metal site on the C-terminal side of the barrel.	2.70101e-14
NZ_LN831790.1|WP_029382702.1|4717835_4718231_-|nitroreductase-family-deazaflavin-dependent-oxidoreductase	gnl|CDD|281995	pfam04075, F420H2_quin_red, F420H(2)-dependent quinone reductase. This family of proteins is found in the genera Mycobacterium and Streptomyces. Member protein Rv3547 has been characterized as a deazaflavin-dependent nitroreductase. Rv1558 is an F420H(2)-dependent quinone reductase involved in oxidative stress protection.	1.90812e-28
NZ_LN831790.1|WP_029382709.1|4727022_4727349_+|antibiotic-biosynthesis-monooxygenase	gnl|CDD|225209	COG2329, COG2329, Uncharacterized enzyme involved in biosynthesis of extracellular polysaccharides [General function prediction only].	1.40614e-21
NZ_LN831790.1|WP_029386175.1|4708514_4708967_+|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	5.44817e-40
NZ_LN831790.1|WP_029382699.1|4713557_4714151_+|hypothetical-protein	gnl|CDD|240430	PTZ00473, PTZ00473, Plasmodium Vir superfamily; Provisional.	0.000567441
NZ_LN831790.1|WP_029386172.1|4706478_4707144_-|pyridoxal-5'-phosphate-synthase	gnl|CDD|235555	PRK05679, PRK05679, pyridoxal 5'-phosphate synthase.	3.09479e-53
NZ_LN831790.1|WP_029386173.1|4707207_4707633_-|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl|CDD|274679	TIGR03618, Rv1155_F420, PPOX class probable F420-dependent enzyme. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomyces, make F420. The Partial Phylogenetic Profiling algorithm identifies this members of this protein family as high-scoring proteins to the F420 biosynthesis profile. A member of this family, Rv1155, was crytallized after expression in Escherichia coli, which does not synthesize F420; the crystal structure shown to resemble FMN-binding proteins, but with a recognizable empty cleft corresponding to, yet differing profounding from, the FMN site of pyridoxine 5'-phosphate oxidase. We propose that this protein family consists of F420-binding enzymes. [Unknown function, Enzymes of unknown specificity].	2.59116e-09
NZ_LN831790.1|WP_029386176.1|4709199_4709835_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	9.90092e-09
NZ_LN831790.1|WP_029382707.1|4725173_4725686_-|DUF2165-domain-containing-protein	gnl|CDD|370754	pfam09933, DUF2165, Predicted small integral membrane protein (DUF2165). This domain, found in various hypothetical prokaryotic proteins, has no known function.	4.45248e-63
NZ_LN831790.1|WP_029382705.1|4721924_4724510_+|bifunctional-FO-biosynthesis-protein-CofGH	gnl|CDD|236422	PRK09234, fbiC, FO synthase; Reviewed.	0
NZ_LN831790.1|WP_029386171.1|4705871_4706474_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.75216e-21
NZ_LN831790.1|WP_029386174.1|4707805_4708432_-|LysE-family-translocator	gnl|CDD|224199	COG1280, RhtB, Putative threonine efflux protein [Amino acid transport and metabolism].	1.16311e-23

Protein sequences

>NZ_LN831790.1|WP_029382699.1|4713557_4714151_+|hypothetical-protein
MNRRVRAVRFTAVSALVVLALTGFSTGRGHGGGHGGEGGGGGGCSSSGQDHDGSSSSSGGGSYQDSGHDDHDDHDGYDPDEYGDYEYRDTGGSGSGGSGSGGTSGSSQLQDAEAELVACATEAEPHAVVEVTNPNTRGGTFRVRVDFTDDETHRALDSAYQDVTLDAAETRRIEVPFHGSVAALDHCEVVPGAAPTR
>NZ_LN831790.1|WP_047121949.1|4711098_4713501_+|PQQ-binding-like-beta-propeller-repeat-protein
MVDQLTQHDPRRIGPFEVLGRLGAGGMGLVYLARSASGRRVAIKTVRTELAEDQLFRVRFTREVEAARAVSGFYTAAVVDADPRAAVPWLATAYVPAPSLEEIVNECGPLPAQAVRWLAAGVAEALQSIHGAGLVHRDLKPSNVLVVEDGPRVIDFGIASGVSNTRLTMTNVAVGTPAYMSPEQAKDSRSVTGASDVFSLGSTLVFAATGHAPFHGANPVETVFMLLREGPDLDGLPDELRPLIESCMQMEPAARPTPADLQAQLAPHLFGSGTDDSGTASAWLPERAVSLIEARRNGRPATQGGGARANAGAVPRPSVPPPPSHDPVIPGPAAPVPPPVPAPVPQPTGSPGTGPVRLPGAPVPIGPGPRVADMRATTVRAPAPESALAASWAKPRPGVNGADPAPAAPAAPPAPAAPPEGAAATGWRPWRFRMSNDVWGTPSVAGDLVYVTSFEVHALDVATGRRRFKTRDVAWSMAVADGRIHASDGPTLFALDAREGTDLWRLSTDAWVYSLKADRGAVVTGTRGGGVQAWEAATGRKLWEITGCQSDFESPEAGPAVHDGTVYVWQNGRLRALDAHGGEERWSYPIGDAASCGGVPVRLTAAPDGCVYVSAGTRVLALDVASGRVKWHFEAPAVFLSPPAFVPGPAVTGGGLYLADYLGTVYALDAADGRDRWRIATEARASVEPVLVAAGHVHVGSGKGLYTLDAVTGTPKWRFQAGGDIVGAPAVAEGRIHFGSTDHLLYTLKADDGRLRWKLATGGEITGSPVVKDGIVYACSKDRCVYALDAEKGTGTARTA
>NZ_LN831790.1|WP_029386176.1|4709199_4709835_-|TetR/AcrR-family-transcriptional-regulator
MRTVDGRVAGRRGQATRQKLLDCLSDMLSSSPYRDVKVIDVARKAGTSPATFYQYFPDVEGAVLEIAEQMASRGAGLAGLVEGRSWAGKAGWQTAQELVDGFLDFWRKNDAILRVVDLGAAEGDKRFNKIRLKILNSVNSSLADAVAELQSKGRVDKDVNPAAIAGALVAMLAAVASHQKGVSSWGVKQAELKPNLALLVHLGVTGKKPAK
>NZ_LN831790.1|WP_029386175.1|4708514_4708967_+|Lrp/AsnC-family-transcriptional-regulator
MDDVDRKILAELQQDGRLTVTELAARVRLSVSPCHRRLRELERSGAISGYRAVVEPAAVGLGFEALVFVSMRQEDRDTVAGFERAVGEVEEVVEAQRLFGEPDYLLRVVAADLAAYQRLYDERLATLPGVQRLNSTLVMKHVVKDRPLPA
>NZ_LN831790.1|WP_029386174.1|4707805_4708432_-|LysE-family-translocator
MDTGTLISFLAVDFLLVCVPGADWAYAISAGLRERSVAWAVGGLVTGYALHTLLAAAGLAVLVAGEPALLTALTVVGAAYLVWLGWGVLHRPATPATTGESAGPASRSRVFLRGATISGLNPKGLLLYLSVLPQFLVTTGTRPAVPAQTAVLGLLHMACCAAVYLTVGLAARAVLGTRPAAARAVTRTSGAAMLGIGAFLLMQRLMTL
>NZ_LN831790.1|WP_029386173.1|4707207_4707633_-|pyridoxamine-5'-phosphate-oxidase-family-protein
MALTREEREQFLAEPHIAALAVDAGAGRAPLTVPIWYQYAPGGEVWIMTGLDSRKNELIRAAGRFSLMVDRVEPTIRYVSVEGPVVRTVPATIEQLREISSRYLPAEKVDEYVDFAWKNHGEQVVVHMRPERWVSTDLGSV
>NZ_LN831790.1|WP_029386172.1|4706478_4707144_-|pyridoxal-5'-phosphate-synthase
MGTDLHELLRSLRVWDPEVTELPPLDPAAAPAAPLPLFERWFADAVAAGEREPHTVSLATADEDGRPDVRIVMLHGADQDGWSFAGHAGSRKGRHLAARPYAALAFYWPVHGRQVRLRGPVAVAPPEEAQADLHARSTGALAAALTGRQSRELGSLEELARASEAAWDRAAREPGTPVESWTLYRLRPEEVEFFQGEPRRRHVRLVYRRTDQGWRRRLRWP
>NZ_LN831790.1|WP_029386171.1|4705871_4706474_+|GNAT-family-N-acetyltransferase
MTTPRLRFRSRPAPELHGHGLRLRAWDPESGAQAEVWLRGVRDPDFLRWNTPLQPVTDLRGARRALRARALDAAEGRSVSFRVTDADSGATLGHVGVDRIDRVLRRARVGYWVLPEARGRGVATRSLLLAARWAFGTLGTHRLELDHALGHHASCRIAERCGFRHEGTLRGAVLQPERHDAFRDAHLHARLATDPEPAVP
>NZ_LN831790.1|WP_047121947.1|4704793_4705282_+|ATP-binding-protein
MQLEIRPDPAEVGRARKWARSRLAVSGIRDDEPLAETLILLVSELVTNAVVHTGCPAVLRLCLPGAATDEATVRLEVADSSDRAPVPRCADDDATGGRGLALVVGLADRWGWSREEGGKRIWCELDRGGQTGPAPGRAGGTGCGPTPGGGASARDGLAFEAV
>NZ_LN831790.1|WP_029386169.1|4703586_4704099_+|EF-hand-domain-containing-protein
MVSSEYERRIAARFTTFDQDGNGYIDREDFNGAAKALLAEFGMAARSDKGQALYGGAEAFWQGMAGMADRDGDQRVTREEFVSGAVKRLSDNPERFAEIARPFLHAALDVADADDDGAVTVEDAARALTALGVEPEAARPVAAALDADGDGKVGEADVVPAFARYFTVSE
>NZ_LN831790.1|WP_029382700.1|4714320_4714515_-|hypothetical-protein
MSDQKTDATATPLDNNMPTPAASDATAATLDNNMPSGPARLDAVTTMDNNMPAPPALDLTRDGK
>NZ_LN831790.1|WP_047121950.1|4714726_4717678_-|tetratricopeptide-repeat-protein
MDGVPRVPEQRGPGSPKESPAALRFGVLGPVRAWRGGEPVATGSPQQRALLAALLLREGRTATAGELIDALWGEDPPSQALAAVRTYASRLRKVLDPGVLVSESGGYAVRGLGDGALDLAVAQELAAEAEKARTAGDLGHAREALGRALALWDGEPLAEVPGPYAEAQRVRLEEWRLQLLETRLDLDLEQGCHAEAVSELTALTAAHPLRERFRELLMLALYRSGRQAEALAVYADTRRLLADELGVDPRPGLRELQQRILQADPGLAEPSAPAAEPAAVPVRPAQLPATVPDFTGRATVVRELSEVLASADGRVMAVSALAGIGGVGKTTLAVHVAHQARPSFPDGQLYVDLQGAGPRPAEPETVLGSFLRALGTPDRAIPDSLEERAALYRSLLDGRRVLVLLDNARDAAQVRPLLPGTDGCAALVTSRVRMVDLAGAHLVDLDVMSPDEALSLFTKIVGRERVASEREAALDVVAACGFLPLAIRIAASRLAARRTWTVSVLAAKLADERRRLDELQAGDLAVKATFELGYGQLEPAQARAFRLLGLADGPDISLAAAAAVLDLPAEETEDLLEALVDTSLLESAAPGRYRLHDLVRLYARACAERDEHPPSEREAALSRLLDFYLATAAGVYAIERPGDRLVEDLEATRYPGLRFDDGSAALDWLYTESAALLACVRQAAGTPRLRRAVDLLWAARDLAESGANFRAYEATAVAMCQATRAAGDLRAEGRARNTLTAVLLVTGRIQRAGEEARLAMECAGSAGDATAASWAAQDRGLIALHQHRYADGKVFFDQAIAGFRAARNGLCEATALCNLSRAYLGMGNTAKAVEFAQHGLAVHVRVGSTMRLANGHYALGVALTAAGRHPEALGQFSEALTIFADHRQRLWEGTTHFRIAEAHIAAHRPSRAAQHAEQALALGCIGGDRTRGSVLTLLGRALSELGQADRAKACWREALHLFEENGASEADAVRLLLAPATAA
>NZ_LN831790.1|WP_029382702.1|4717835_4718231_-|nitroreductase-family-deazaflavin-dependent-oxidoreductase
MPHLADLRFRAATTFQRRVANPLLRRLPLQTVLETTGRVSGLPRRTPVGGRRAGNSFWLVAEFGERAQYIRNIRADPRVRVRLGGRWHPDTAHPLPDDDPVVRLRTLPRFNSAAVRLFGTDLMTVRVDLDR
>NZ_LN831790.1|WP_029382703.1|4718515_4720060_+|APC-family-permease
MTQAVMRTPVGDEADGVRGKGLGGNSVGLLGSAVIGVSTVAPVYCLTSTLGSTAGEVGVQLPAIFLVGFLPMLLVAFAYRELNKAVPDCGTSFTWTVKAFGPSVGWMCGWGLVIATVIVLSNLAGVATSYFWLLAGELTGSQAVADLDGNKAVHILTCLALIAAATAVSYRGMTATKGVQYALVALQLVVLALFVVFAFGKAGSGSFPGHLDFSWSWLNPFEVGSFATFSAGLSLSIFMYWGWDACLTANEETVGSEKTPGRAALISMVVLVGSYLVTAVAAQMAVGSGTEGLGLANPETSDNVFAALAGPVMGDGLGILLFVAVLASAAASLQTTFIPVARTVLAMAAYEALPPSYARVHEKFRTPGRATVTAGVATAVFYTVMTLVSEHVLVDTIYALGLMICFYYALTAFACAWFFRGELTRSPRDALFKGVLPVLGGISLTAVFCKTLYDMWNPEYGSGSSVFGVGSVFVIGVGLLLLGLVIMLVMRRRSPAFFRGEVLTTSTPALVVED
>NZ_LN831790.1|WP_029382704.1|4720079_4721606_-|PHP-domain-containing-protein
MCEDHPSEAGIGRRAVFVTGAAAALTLGTVSFASAEGRDRDQDRETRTVRGTLPPGSPDFVYVPVEVPAGVREIRVAYSYDRPPVPAGTPGNALDIGLFDERGTELGGRGFRGWSGGARTEFFVRADEATPGYLPGPVREGTWHIALGPYTVAPQGLSYELTVTLVYGEPGRTPEPVYPPERARGRGRAWYRGDCHLHSWHSDGRRTPAEIAALARAAGLDFINSSEHNTHSAHAHWAEAAGDDLLVMLGEEVTTRNGHVVALGTDPGTFVDWRYRARDNRFGRFARQIRRAGGLVVPAHPHATCIGCNWKFGFGEADAVEVWNGPYTPDDEVALADWDGMLVASVREGRAWIPAMGSSDAHRDPDVVGRPQTVVLADDLTRRAIQEGIRAGRSYVAESAQVSLSFTASGGRGEHAGIGERLRVDRDAPVTVRLEVTGAPRCTVRLVTDQGVLHTSAPLPVSGSGTVEWRTTASYAAYVRAELRHEAAAGPVPGALAAFTNPIFLGSR
>NZ_LN831790.1|WP_029382705.1|4721924_4724510_+|bifunctional-FO-biosynthesis-protein-CofGH
MTISATSGTGPTENSMRRALKRARDGVALDVSEAAVLLQARGEHLDDLAASAARVRDAGLGAAGRPGVITYSKSVFIPLTRLCRDKCHYCTFATVPGKLRRAGHGMFMSPDEVLDIARKGAALGCKEALITLGDKPEDRWPEAREWLDAHGYDDTIAYVRAVSIRILEETGLLPHLNPGVMTWTDFQRLKPVAPSMGMMLETTATRLWSEPGGPHHGSPDKEPAVRLRVLEDAGRSSVPFTSGLLIGIGETYEERAESLFALRRISRAYHGIQELIIQNFRAKPDTAMRGMPDAELDELVATVAVARHIMGPAACLQAPPNLVDAEYERLIGAGIDDWGGVSPLTIDHVNPERPWPQIDELAEKSRAAGFELRERLCVYPEFVRRGEPWLDPRLRPHVTALADPETGLARADAVVEGRPWQEPDEVFTATGRTDLHATIDTEGRTADRRDDFDEVYGDWGALREAAAPGMAPERIDTDVRAALATAADDPTRLTDDEALALLHADGPALDALCRVADDVRKSAVGDDVTYIVTRNINFTNVCYTGCRFCAFAQRRTDADAYTLSLDQVADRAQQAWEVGAVEVCMQGGIHPDLPGTAYFDIARAVKARVPGMHVHAFSPMEVVNGATRTGMSIREWLTAAKEAGLDSIPGTAAEILDDEVRWVLTKGKLPTATWIEVVETAHELGIRSSSTMMYGHVDQPRHWLGHLRTLVGIQQRTGGFTEFVTLPFIHTNAPVYLAGIARPGPSMRDNRAVTAMARLLLHPYIPNIQTSWVKLGTEGAAEMLRSGANDLGGTLMEETISRMAGSSYGSYKSVRDLIAVAEAAGRPARPRTTLYGEVPEERQRAARESDGHLPELLPVLD
>NZ_LN831790.1|WP_029382706.1|4724632_4725190_+|hypothetical-protein
MPARLPSWAWVSGLTVGAIAAVSVLAVQADRGPRPAAAPVARPGPTVSAHPSPKESPTPAVPDGSGTGRRIVYSLGDDRVWLVDASDATRRSFTVWPGTVDPDPGSYLVGSRRDATTGSDGVPIEHIVYFALKDGVNVAFSNAVDGSSPPPPPSGAKTGGIRVHKADGTALWAFATKGTEVTVVG
>NZ_LN831790.1|WP_029382707.1|4725173_4725686_-|DUF2165-domain-containing-protein
MAPTSRTLPLAAGLLTGTAALYITLVALGNITDFGTNQQFVRHVLAMDTTFKDEDLMWRAITTEWIQDAAYVLIIVWETVAALVLLYGTWLWFRHDHPRARRISTYGLLMLMLLFGAGFIAIGGEWFAMWQSDTWNGLDAATRVFLLSGVVLLVNHLPTGQERDGATRRP
>NZ_LN831790.1|WP_049976748.1|4725775_4726852_-|tyrosine-protein-phosphatase
MDHTTRVKAARVLPAAALLVGLAAPAAAAAPAHHPGHGAQRIPFTAAEVTARDDGSYTVTWKAPGVRHVAVRANGRTVASGGATGTVTVKGLPAADRQWFDLVPAHGGALRLADRLIELDGTVNFRDAGGYRTKDGRWVKMGVVYRSDSLDKLTDADLAKLKRLGLAADYDLRTTAERTDAPDRVPEGTRYVAANVLGDGSPVFSLPKTAAEAERLMIDVEKSMVGAASAKAAYSSVFADLADGDPDGTLYHCTAGKDRTGWASAALLTALGVPRETVMADYLASNDYRAEANAAALAALPAEQAAVYKPMLDVRAAYLNSGFAEVERAYGSFAAYEKKALGLDARELRALRAGLLTG
>NZ_LN831790.1|WP_029382709.1|4727022_4727349_+|antibiotic-biosynthesis-monooxygenase
MSVVKINVLTVPAEQRETLEKRFASRAHAVESSDGFEWFELLRPVEGTDQYLVYTRWRDEASFQAWMEGPMKTAHQGGGEGGDRPKPAASGSTLWSFEVVQQAAPKSE

Crispr_ID: NZ_LN831790_10

• CRISPR_ID: NZ_LN831790_10
• CRISPR_location: 5015153-5015307
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_LN831790_10

Consensus_repeat	Method
GCCGGGCCCGCGGCTACGCGCGCGCGGGCAGGTG	PILER-CR
CCCGCGGCTACGCGCGCGCGGGCA	CRISPRCasFinder

spacers of NZ_LN831790_10

>10.1|5015187|28|NZ_LN831790|PILER-CR
GAAGGGGCCGCGACTGAAGCCCGTTTCC
>10.2|5015249|27|NZ_LN831790|PILER-CR
CCGCACCACGGGAACGAGATCGCCCAG
>10.3|5015181|38|NZ_LN831790|CRISPRCasFinder
GGTGGAAGGGGCCGCGACTGAAGCCCGTTTCCGCCAGT
>10.4|5015243|37|NZ_LN831790|CRISPRCasFinder
CGTGCCGCACCACGGGAACGAGATCGCCCAGGCCGGG

CRISPR arrays and Neighbor proteins around NZ_LN831790_10

CRISPR arrays

The CRISPR arrays of NZ_LN831790_10

>merge|NZ_LN831790|10|5015153-5015307|PILER-CR,CRISPRCasFinder
CGGGCCCGCGGCTACGCGCGCGCGGGCAGGTGGAAGGGGCCGCGACTGAAGCCCGTTTCCGCCAGTCCCGCGGCTACGCGCGCGCGGGCACGTGCCGCACCACGGGAACGAGATCGCCCAGGCCGGGCCCGCGGCTACGCGGGCGCGGGCAGGTA

>NZ_LN831790|10|1|5015153-5015307|PILER-CR
CGGGCCCGCGGCTACGCGCGCGCGGGCAGGTGGA	AGGGGCCGCGACTGAAGCCCGTTTCCGC
CAGTCCCGCGGCTACGCGCGCGCGGGCACGTGCC	GCACCACGGGAACGAGATCGCCCAGGC
CGGGCCCGCGGCTACGCGGGCGCGGGCAGGTA

>NZ_LN831790|10|10|5015157-5015303|CRISPRCasFinder
CCCGCGGCTACGCGCGCGCGGGCA	GGTGGAAGGGGCCGCGACTGAAGCCCGTTTCCGCCAGT
CCCGCGGCTACGCGCGCGCGGGCA	CGTGCCGCACCACGGGAACGAGATCGCCCAGGCCGGG
CCCGCGGCTACGCGGGCGCGGGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029383063.1|5003914_5004703_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831790.1|WP_029386445.1|5021719_5026660_+|NAD-glutamate-dehydrogenase	unknown	unknown	gnl|CDD|377452
NZ_LN831790.1|WP_029383070.1|5012252_5012945_+|ribosome-associated-translation-inhibitor-RaiA	unknown	unknown	gnl|CDD|238308
NZ_LN831790.1|WP_176572962.1|5008747_5010559_+|GerMN-domain-containing-protein	unknown	unknown	gnl|CDD|237447
NZ_LN831790.1|WP_029383066.1|5005967_5006645_+|two-component-system-response-regulator-MtrA	unknown	unknown	gnl|CDD|223816
NZ_LN831790.1|WP_029386450.1|5033302_5034220_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_LN831790.1|WP_047121976.1|5019052_5019637_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383067.1|5006646_5008725_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|223715
NZ_LN831790.1|WP_047121978.1|5032464_5033310_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213187
NZ_LN831790.1|WP_029383069.1|5010732_5011944_+|ComF-family-protein	unknown	unknown	gnl|CDD|223970
NZ_LN831790.1|WP_029383064.1|5004711_5005461_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|132997
NZ_LN831790.1|WP_047121977.1|5028388_5030095_-|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|366154
NZ_LN831790.1|WP_029386444.1|5020550_5021225_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223620
NZ_LN831790.1|WP_047122599.1|5026926_5028384_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029386448.1|5030091_5032317_-|CDP-glycerol-glycerophosphotransferase-family-protein	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029386443.1|5019934_5020450_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029383065.1|5005619_5005832_+|ferredoxin	unknown	unknown	gnl|CDD|379145
NZ_LN831790.1|WP_029383072.1|5013898_5015071_-|YcaQ-family-DNA-glycosylase	unknown	unknown	gnl|CDD|225755
NZ_LN831790.1|WP_029383071.1|5013150_5013897_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_LN831790.1|WP_029383074.1|5016140_5018957_+|preprotein-translocase-subunit-SecA	unknown	unknown	gnl|CDD|237259

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029383063.1|5003914_5004703_+|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	1.93617e-41
NZ_LN831790.1|WP_029386445.1|5021719_5026660_+|NAD-glutamate-dehydrogenase	gnl|CDD|377452	pfam05088, Bac_GDH, Bacterial NAD-glutamate dehydrogenase. This family consists of several bacterial proteins which are closely related to NAD-glutamate dehydrogenase found in Streptomyces clavuligerus. Glutamate dehydrogenases (GDHs) are a broadly distributed group of enzymes that catalyze the reversible oxidative deamination of glutamate to ketoglutarate and ammonia.	0
NZ_LN831790.1|WP_029383070.1|5012252_5012945_+|ribosome-associated-translation-inhibitor-RaiA	gnl|CDD|238308	cd00552, RaiA, RaiA ("ribosome-associated inhibitor A", also known as Protein Y (PY), YfiA, and SpotY, is a stress-response protein that binds the ribosomal subunit interface and arrests translation by interfering with aminoacyl-tRNA binding to the ribosomal A site. RaiA is also thought to counteract miscoding at the A site thus reducing translation errors. The RaiA fold structurally resembles the double-stranded RNA-binding domain (dsRBD).	6.10306e-26
NZ_LN831790.1|WP_176572962.1|5008747_5010559_+|GerMN-domain-containing-protein	gnl|CDD|237447	PRK13613, PRK13613, lipoprotein LpqB; Provisional.	0
NZ_LN831790.1|WP_029383066.1|5005967_5006645_+|two-component-system-response-regulator-MtrA	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	3.09993e-88
NZ_LN831790.1|WP_029386450.1|5033302_5034220_-|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	1.69115e-36
NZ_LN831790.1|WP_029383067.1|5006646_5008725_+|HAMP-domain-containing-protein	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.47499e-57
NZ_LN831790.1|WP_047121978.1|5032464_5033310_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	4.67802e-98
NZ_LN831790.1|WP_029383069.1|5010732_5011944_+|ComF-family-protein	gnl|CDD|223970	COG1040, ComFC, Predicted amidophosphoribosyltransferases [General function prediction only].	6.82803e-16
NZ_LN831790.1|WP_029383064.1|5004711_5005461_+|glycosyltransferase-family-2-protein	gnl|CDD|132997	cd00761, Glyco_tranf_GTA_type, Glycosyltransferase family A (GT-A) includes diverse families of glycosyl transferases with a common GT-A type structural fold. Glycosyltransferases (GTs) are enzymes that synthesize oligosaccharides, polysaccharides, and glycoconjugates by transferring the sugar moiety from an activated nucleotide-sugar donor to an acceptor molecule, which may be a growing oligosaccharide, a lipid, or a protein. Based on the stereochemistry of the donor and acceptor molecules, GTs are classified as either retaining or inverting enzymes. To date, all GT structures adopt one of two possible folds, termed GT-A fold and GT-B fold. This hierarchy includes diverse families of glycosyl transferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. The majority of the proteins in this superfamily are Glycosyltransferase family 2 (GT-2) proteins. But it also includes families GT-43, GT-6, GT-8, GT13 and GT-7; which are evolutionarily related to GT-2 and share structure similarities.	5.31656e-13
NZ_LN831790.1|WP_047121977.1|5028388_5030095_-|glycosyltransferase-family-2-protein	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	2.8233e-33
NZ_LN831790.1|WP_029386444.1|5020550_5021225_+|HAD-family-hydrolase	gnl|CDD|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	8.81e-29
NZ_LN831790.1|WP_029386448.1|5030091_5032317_-|CDP-glycerol-glycerophosphotransferase-family-protein	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	9.20299e-158
NZ_LN831790.1|WP_029383065.1|5005619_5005832_+|ferredoxin	gnl|CDD|379145	pfam13370, Fer4_13, 4Fe-4S single cluster domain of Ferredoxin I. Fer4_13 is a ferredoxin I from sulfate-reducing bacteria. Chemical sequence analysis suggests that this characteristic [4Fe-4S] cluster sulfur environment is widely distributed among ferredoxins.	1.636e-07
NZ_LN831790.1|WP_029383072.1|5013898_5015071_-|YcaQ-family-DNA-glycosylase	gnl|CDD|225755	COG3214, COG3214, Uncharacterized protein conserved in bacteria [Function unknown].	3.55023e-73
NZ_LN831790.1|WP_029383071.1|5013150_5013897_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	4.44443e-77
NZ_LN831790.1|WP_029383074.1|5016140_5018957_+|preprotein-translocase-subunit-SecA	gnl|CDD|237259	PRK12904, PRK12904, preprotein translocase subunit SecA; Reviewed.	0

Protein sequences

>NZ_LN831790.1|WP_029383072.1|5013898_5015071_-|YcaQ-family-DNA-glycosylase
MTTPRATAELTADEARRIALRAQGLLGAPDRRSGVRGVLRRLGAVQLDTISVLARSHELVPYARLGAVGRTTVEDAYWKDTHAFEYWSHAACILPVEEWPHFAFRRRAYRDRPHWNHELPEGVYERVVKQLRAEGPLTATELGGAKRTGEWWDWSASKVAVERALMYGEVVCVERRGWKRVYDLAERAIPASLLHDELDDTECLRRLVRLAGQALGVGTRADIADYHRLKGEQVDAVIAESGLVPVTVEGWGRPAWADPAALQSPPRGRHRTTLLSPFDSLVWERARTERLFGFTHRLEAYVPRHKRVYGYFTMPVLAGGRLVGRVDPAREGRALVARQVTLEGPKAVPAVAQALVEAAGWVDCTDVRVERVDAPELRDALVKELARALA
>NZ_LN831790.1|WP_029383071.1|5013150_5013897_+|response-regulator-transcription-factor
MADSFGPMRDEDAGEGVVGMGPDAGCAREEPIRVLVVDDHALFRRGLEIVLAAEEDIQVVGEAGDGAEAVEKAADLLPDIVLMDVRMPKRGGIEACTSIKEVAPSARIIMLTISDEEADLYDAIKAGATGYLLKEISTDEVATAIRAVADGQSQISPSMASKLLTEFKSMIQRTDERRLVPAPRLTDRELEVLKLVATGMNNRDIAKELFISENTVKNHVRNILEKLQLHSRMEAVVYAMREKILEIR
>NZ_LN831790.1|WP_029383070.1|5012252_5012945_+|ribosome-associated-translation-inhibitor-RaiA
MDIVVKGRKTEVPERFRKHVAEKLKLDKIQKLDGKVISLDVEVSKEPNPRQADRCDRVEITLRSRGPVIRAEAAASDPYAALDLAAEKLDARLRKQHDKRFSRRGSRRIPAAEVADHVPGAATLNGAGAVVPQDEQESVPTKKIGSLEIQGEGPLVVREKTHVAAPMTLDQALYEMELVGHDFYLFVDSETKEPSVVYRRHAYDYGVIHLRTDTMVTQAPSPEAGGALGG
>NZ_LN831790.1|WP_029383069.1|5010732_5011944_+|ComF-family-protein
MRGWWRDLTDLVLPAECGGCGRARTVLCPRCRAALSGAAPRRVRPEPEPPGLPPVHAAARYADEVRAVLLAHKERGALALAGPLGTALAGAVRAGLRAAGLREASTGAYGALETGVAGAVEAGAHRAVETGALGAVGAGAHGAVDTDGLGSVETGAFGSVETCGPGGLGFPGDGAGGAVGRGGAGWRADRVAGAGGSGVRGERAVLLVPVPSARRAVRARGHDPARRIALAAAGELRRSGTPARMLAALRHRRAVADQSGLDSRQRWDNLAGALAVVPGAARLLCGAAAVVLVDDLMTTGASLAEAARAVRASAGGGAGPAGRAGLPAGRTTGPGAHMTGMAAVYSWAMGEGRGERMGTAPEERTDRAPAGPDRTGADGGTIRRVMCAAVVAASPEAFGINRN
>NZ_LN831790.1|WP_176572962.1|5008747_5010559_+|GerMN-domain-containing-protein
MPVRAVAYAVGGAVLLAGCASMPDSGDLRGVESTPRQDTQVRVFAMPPAENAPPSEIVQGFLEALTSDDPHFETAREYLTDKARKTWRPELSTTVLADGPGTEPGRVGDREDADAYSLTLTGTKVATVDAQQSYAPADGEYRAPVHLTRDAKTGQWRIDTVPQGVVLGKSDFQRNYMSVNKYYFAANETQDAADGAGGEPMAVADPVYVRKRVDPLTQAVRSLLSGPTRPLGPAVRTSFPAGTALAEGVSSLTPDDRNRLTVELNGRAARTGPDTCDEMAAQLLFTLRNLTPAVDEVDLRSGDTRLCSLTEDRAAAVAARGSAQHPDYLYFVDGEERVVRLPAGSSATRAEPVPGALGSGAAKLRSVAVSRDEHRAAGVGLDGGSLYVASLVSGASLGERVLTSEGPTEGERLSTPSWDAQGDLWVVDRDPAGPRLLMLEDGAGRPVTVRTPGLEGRVQDVRVAADGVRIALVVRDEDGQRSLLIGRIARDGKTGGEQAVTVRGLRSATPGLEEVTAMSWAGDSRLVVVGREHGGVQQIGYVQVDGSTPEPQAPAALTGVQEIAASEDERMPLVAYSEDGIVRLPSGTQWQKVTDGTAPVYPG
>NZ_LN831790.1|WP_029383067.1|5006646_5008725_+|HAMP-domain-containing-protein
MSGDSAASVPGRSGARAGRPVGRKAGGSRGRRFLEGGLLHGGVQGSPVLRLFMRWVRRPLLPVIRLWRRNLQLKVVVTTLLMSLGVVLLLGFVVIGQVRNGLLDAKVKASQSQATGGFAAAKQRADEAATAAGDAGTPVNDRPSQNVIQWMSDLVYSLSSGGQGAFDVVTLPAVGDSGGGRGPRASGDVAPSASIPESLRERVDSSTAAAQSYTRIVYNSSEASQPALVIGKRVNDPNGDPYQLYYLFPLTQEEKSLSLVKGTLATAGLFVVVLFGAIAWLVVRQVVTPVRMAAGVAERLSAGRLQERMKVTGEDDIARLGEAFNKMAQNLQLKISQLEDLSRMQRRFVSDVSHELRTPLTTVRMAADVIHEAREDFDPVTARSAELLADQLDRFESLLADLLEISRFDAGAAALEAEPIDLREVVRRVVSGAEPLAERKGTRIRVTGDQQPVVAEADARRVERILRNLVVNAVEHGEGRDVVVKLASAGGAVAVAVRDYGVGLKPGEATRVFSRFWRADPARARTTGGTGLGLSIALEDARLHGGWLQAWGEPGGGSQFRLTLPRTADEPLRGSPIPLEPADSRGRRAAEETAPADGGAKAATVPAQQSAGPGPARPARDPIPSRPAGASPAADPTALPGNGARVVPRPVSPARRQDGPSAAEPSAAHGDEHPAGRPEEDPNSQGEACRGR
>NZ_LN831790.1|WP_029383066.1|5005967_5006645_+|two-component-system-response-regulator-MtrA
MKGRVLVVDDDSALAEMLGIVLRGEGFEPSFVADGDKALAAFREAKPDLVLLDLMLPGRDGIEVCRLIRAESGVPIVMLTAKSDTVDVVVGLESGADDYIVKPFKPKELVARIRARLRRSEEPAPEQLAIGDLVIDVAGHSVKRDGQSIALTPLEFDLLVALARKPWQVFTREVLLEQVWGYRHAADTRLVNVHVQRLRSKVEKDPEKPEIVVTVRGVGYKAGPS
>NZ_LN831790.1|WP_029383065.1|5005619_5005832_+|ferredoxin
MKVSVDQNLCYGSWDCVHRVPSVFTVVDGFGAVVPGREEAGDDPRVRAAAEGCPSQAIVITDGRAAGPAM
>NZ_LN831790.1|WP_029383064.1|5004711_5005461_+|glycosyltransferase-family-2-protein
MTNLVSVITPVHGPGARYLAEAHASLTRQEMPPGWDWEWIIQEDGETGDVRPHVPADPRISFEQGRRGRAGMARTLGLARARGELVKVLDADDMLTPGALRRDIEVLTEQRGVAWTTSRVLDLLPDGSTVGFDSDPPAGPITQGAVLERWRTHDYRSPVHPATLCARRDLVIALGGWMALPSSEDTGLLMALNAVSTGWFVEECGLLYRKWPGQSTAQSGHHDEAERRARMKVVEERAEALGKLSTWHL
>NZ_LN831790.1|WP_029383063.1|5003914_5004703_+|GntR-family-transcriptional-regulator
MAKRCEQVSGDLRRRIRAGEFLPGDRLPAETTLVTEYEVGLVTVREALAALRTEGLIEERHGRGTFVRGRRRRAERSNLRHQWEKDRARAGPGERRSTGATEEDTGLTTDQLAFQAEYERIEAPEELAAALGLEPGDAVLKRTYRTRSVDEDDSLKVARSYIPYEIAEQNPDLLDAGQEPWPGGTMNQLFTVGIEIDRVEEVVTARSPTPEESEELGLTPGAAIMDVRKTLYDIDGRIVEVADVVLPGDRYAVKCVTTLERW
>NZ_LN831790.1|WP_029383074.1|5016140_5018957_+|preprotein-translocase-subunit-SecA
MSVLSKIMRAGEGKILRRLHRIADQVNSIEEDFVDLSDAELRALTDEYRQRYADGESLDDLLPEAFATVREAAKRVLGQRHYDVQLMGGAALHMGYVAEMKTGEGKTLVGTLPAYLNALSGDGVHIVTVNDYLAERDSEMMGRVHRFLGLSVGCILASMTPAQRREMYACDITYGTNNEFGFDYLRDNMAWSKDELVQRGHNFAIVDEVDSILIDEARTPLIISGPADQATKWYGDFAKLVKRLKRGEPGNPLKGLEETGDYDVDEKKRTVAIHEAGVAKVEDWLGIDNLYESVNTPLVGYLNNAIKAKELFKKDKDYVVIDGEVMIVDEHTGRILAGRRYNEGMHQAIEAKEGVEIKDENQTLATITLQNFFRLYNKLSGMTGTAMTEAAEFHQIYKLGVVPIPTNRPMIRKDQSDLIYRTEVAKFEAVVDDIEEKHRKGQPILVGTTSVEKSEYLSQQLSKRGIQHEVLNAKHHEREASIVAQAGRKGAVTVATNMAGRGTDIKLGGNPEDLAEAELRQRGLDPEEHIEEWAHALPEALKRAEEAVKAEKEEVEKLGGLYVLGTERHESRRIDNQLRGRSGRQGDPGESRFYLSLGDDLMRLFKAQMVERVMSVANVPDDVPIENKMVTRAIASAQSQVETQNFETRKNVLKYDEVLNRQREVIYGERRRVLEGEDLHEQIQHFMNDTIDAYVQAETAEGFPEDWDLDRLWGAFKQLYPVKVTIEELEEAAGDRAGLTAEFIAESVKDDIHQQYEAREAQLGSEIMRELERRVVLSVLDRKWREHLYEMDYLQEGIGLRAMAQKDPLVEYQREGFDMFQAMMDGIKEESVGYLFNLEVQVEQQVEEVPVEAAAPSLDKGPQDQVPAQAGPRPEIRAKGLDAPQRRNLHLTAPTVDGEGGVIEREVTADDEPVRSPADGLTRAERRKQAKGGRRRKK
>NZ_LN831790.1|WP_047121976.1|5019052_5019637_-|hypothetical-protein
MHKVMTRAHQRPGSTRPSHRRDPRGPGAAPPRAPGGGATRATAPRGRRPGSPGEPPRAGTGPLDTRPPGRETVPGARRPLPQPRPTDMFAELLVGVLSGRRPVHSMLRHTAGRAYDELAWLAEHHPLRTRGTHPVVRDIGYFEPRPGAVEVFARIGAGDRLRALAFRLERGRDLRWRCTAVELGGPRMPRGDDG
>NZ_LN831790.1|WP_029386443.1|5019934_5020450_+|hypothetical-protein
MRVYVPLTLPGLAEAYQKGELGAAPLVAYAVTPALREWYLSDDIEELEYAALSRAALASLRLLAADPEAARRRVVVAVDVPDGAASADPGRGLDPAALGEVRVTGAVPLAKAASVHVDAADAEADVAAAAEALKAADAGDDDAQFVVDGSEDHELLWYATQEIPNLVGNAG
>NZ_LN831790.1|WP_029386444.1|5020550_5021225_+|HAD-family-hydrolase
MGTNSAAHIVWDWNGTLFHDNDAVIGATNAAFAELGLEPITLEQYRAMYCVPVPKFYERLLGRLPSEAEWEVMDETFHRHYAEHRVRCGLAEGAAELLTGWRSAGRSQSILSMYGHEELIPLVRGFGIEAHFIRIDGRTGPSGGSKAEHMVRHLDSLAGETGVDPARTVVIGDAADDALAALHVGARAVLYTGGSHSRVSLESAGVPVVDTLHEAVAEAERLAA
>NZ_LN831790.1|WP_029386445.1|5021719_5026660_+|NAD-glutamate-dehydrogenase
MQTKLDEAKAELLERAARVAENSPVGGHLPTGTTSEGTPDTPDRESVLAFLQRYYRHTAPEDLADRDPVDVFGAAFSHYRLAGNRPQGTANVRVHTPTVEENGWTCSHTVVEAVTDDMPFLVDSVTNELTRQGRGIHVVVHPQFVVRRDVTGKLIEVLTTPPSGELPHDAHIESWIHVEIDRETDRADLKQITADLLRVLSDVREAVEDWGKMRDAAMRLADSLSGESLPGDLPRPEVEEARELLHWLAEDHFTFLGYREYELRGDDSLAAVPGTGLGILRADPHHAAEDSHPVSPSFERLPADARAKAREHRLLVLTKANSRATVHRPSYLDYVGVKKFDEKGNVVGERRFLGLFSSAAYTESVRRVPVIRRKVQEVLSRAGFSPNSHDGRDLLQILETYPRDELFQTPADELQAIVTSVLYLQERRRLRLYLRQDEYGRYYSALVYLPRDRYTTGVRLRIIDILKEELGGTSVDFTAWNTESILSRLHFVVRVPQGTELSELSDADKERIEARLVEAARSWADGFAEALNAEFGEERSAELMRRYGSAFPEGYKADHSPRAAVADLAHLEQLDDERTFALSLYEPVGAGPEERRFKIYQKGGSVSLSAVLPVLSRLGVEVTDERPYELRCGERRTAWIYDFGLRMPKAAAAAGDYLGDDARERFQDAFAATWTGKAENDGFNALVLSAGLTWRQAMVLRAYAKYLRQAGSTFSQDYMEDTLRNNVHTTRLLVSLFEARMSPERQRAGREIVDALLEELDAALDQVASLDEDRILRSFLSVIKATLRTNFFQEAAPGRPHDYVSMKFDPQAIPDLPAPRPAFEIWVYSPRVEGVHLRFGKVARGGLRWSDRREDFRTEILGLVKAQMVKNTVIVPVGAKGGFVAKQLPDPSVDRDAWMAEGIASYKTFISALLDITDNMVAGEVVPPKDVVRHDEDDTYLVVAADKGTATFSDIANEVAGTYDFWLGDAFASGGSAGYDHKGMGITARGAWESVKRHFRELGVDTQSQDFTVVGIGDMSGDVFGNGMLLSEHIRLVAAFDHRHIFIDPTPDAAVSYAERRRLFELPRSSWEDYDTALLSPGGGVFPRTAKAIPVNAHIREALGIEEKVSKMTPADLMKAILKAPVDLLWNGGIGTYVKASTESHGDVGDKANDAIRVDGQDLRVKVVGEGGNLGLTQLGRIEFAMQGGRVNTDAIDNSAGVDTSDHEVNIKILLNGLVADGDMTVKQRNKLLAEMTDEVGRLVLRNNYAQNTAIANALAQSKDMLHAQQRFMRHLVREGHLDRALEFLPTDRQIRERLSAGQGLTGPETAVMLAYTKITVAEELLHTSLPDDPYLKGLLHAYFPTALRERFGDRIDTHPLRREITTTVLVNDTVNTGGTTYLHRLREETGASLEEIVRAQTAARAIFRAYPVWDAVESLDNKVEAAVQTRIRLHSRRLVERGTRWLLNNRPQPLQLAETVDFFAERVEQVWQELPKLLRGADLEWYQYIHDELTAAGVPEELATRVAGFSSAFPTLDIVSVADRMGKEPLDVAEVYYDLADRLTITQLMDRISALPRTDRWQSMARAAIREDLYAAHAALTADVLAVGDGTSTPEERFRVWEQKNAAILARARTTLEEIQSSDAFDLANLSVAMRTMRTLLRTHS
>NZ_LN831790.1|WP_047122599.1|5026926_5028384_+|hypothetical-protein
MPLALLPLVPLLVLLVLVVVRLPWAGDLGIHAATVERLRHSLGDPGNPLVDADTPSPYYSPWTLLLGAVARASGLSVFVVLRLGALVALGLLVTGVWRYVRTLSAHRAAPALALLSLPLLWGTVPFTWSGFLGLHSLALTVAYPSVFALGLAFHLWAWLARAPRDGGRTGWGTWAGLGALWAVVLLCHQFTGVVASLGALATVLAARPARAVTAGTAAAAAAGLAVLWLWPYYDFFALFGAGDGLEAVHRPLYTDLPGRFGLVLLGVAALALRLRRDRRDPLVLFFALGLLVSAAGGLSGHYSWGRALPAALIPAQLAAALEAVEAGRRAVRAAWACLLAGALAVGAWTQAGTLGYVVDRGVLPGPVAAKYRPPWAGYHWITPWVRYGDVVMARTFPSRQIPAYGAYTVAPGYPDFFLPDEERRAAAVRRYFAAGTPPKERREIVREYGVRWVVDRGPAPRTEPGLRAVARGPGGQVLYAVPDAG
>NZ_LN831790.1|WP_047121977.1|5028388_5030095_-|glycosyltransferase-family-2-protein
MNPRTGPETAPGTPPAAPDVTVTVIVYNDAGRLPRAVASVRRQTHPNIEIVISDDHSTDDTPRVARELAARDPRIRYLRLPENSGGCSAPRNRALEIARAPYLMFLDSDDELPERAVEVLLAAHRAREIDFAMGAVRRVRVDTGRHSTWMPHLVAEHRTLEGVEADPRLFFEHLSTGKMYARAFLDRHGLRFPEGIHYEDQLFSAQAYCLAKTFTIVPEPVYRWYVAPYADAGAASISNQRHKLANVRDRIHVQRLIDAFLAESGHESLREDKDYKFLKHDFRMYAGDLPLRDEEWLASFADTVGPYLDTLSEGAYARLPRDERIVVELVRDRRLADAREAARGLGHDVAPPRVTTGPDGRTYWGGHVPDSERARRELDVTGLELDTRPFVVARFRHEITELDRGPGASVDLTIRTHDPGLRLPVGPQRATLLLTPGRQRLAVAFRLSPVRPGVFEGRVHLDLAAARLPLRGFTGVRHPVLRLHHRGRAHTGILLAPPAFPPFTTRVARRSGAAPHRITVEPEGHAPGRLQVRWQPAGAAARMLRPVLRRIARPGVRRAALLVRSVLR
>NZ_LN831790.1|WP_029386448.1|5030091_5032317_-|CDP-glycerol-glycerophosphotransferase-family-protein
MPETRETAPDPGPVLSVVVHGPNVQDHLTGLLESLAARPLPDTEVIVAAVGDWARETAERHGPALQVLALPDGTGDAAARAAGAARAGGRWLHFVHAKDGLPAGAPRLVADRAAELPGTVDVLLLDHVHSTWRASALPSRDGPLLARAGGADLALDDQPRLLRLAPLLGTRVLRAGFWRRHGELFATDDEPFAAYAALLLAGRVACLPHPAYEDRRLRPESLPPVAPEQHHALIDRYERLLGLTRDRPAAHAVLYDVMVRDCLRVFVRAGMPPTTAREFFRRASLAALRRRPEDYRRPAGLEGIRRTLLEEDAYTGYRALQAANRARRAVRTAVRSGRRQAGARLRDLEYRRALGRPVDPRLAVFSAYWDRGVACNPAAIAAKLAELAPHIHPVWVVTAGNAALLPPGTDHVVPGTGRYREVLARAAYLVNNVNFPNGVVKRPDAVHVQTHHGTPLKRMGLDQMPYPAAARGLDFRALLERVDKWDYSVSANSHTTRMWQRAYPSRYVSLDHGYPRNDVYYTAGAGEVRAVRERLGIPPGHRAVLYAPTHRDYEAGFTPRLDLAALADRLGEKTILLVRAHYFYDGGLSPLTGLRRTGRIVDVSAYDPVEELCLAADALVTDYSSIMFDYANLDRPIVIHADDWETYRTTRGVYFDLMTGAPGPVARTQEELTEILATEAWRDGAAATARAAFRRRFCEYDDGRAAERVVRRVFLGQDEATLPPVLPLERRTPAPRPEEVM
>NZ_LN831790.1|WP_047121978.1|5032464_5033310_-|ABC-transporter-ATP-binding-protein
MAEHTRRIPHEAAPEGADRVPTVIADGVDIVYRVNGAAQGRGTATAALNRILRRERAGRAAGVRRVHAVRNVSFVAYRGEAIGLIGTNGSGKSTLLKAVAGLLPVENGRIYTDGQPSLLGVNAALMNDLTGERNVHLGGLAMGMSREQIRERYQDIVDFSGINDKGDFITLPMRTYSSGMAARLRFSIAAAKDHDVLLVDEALATGDRSFQKRSEERIRELRERAGTVFLVSHSNKSIRDTCDRVLWLERGELRMDGPTAEVLKEYEAFTGGPDRAARPKS
>NZ_LN831790.1|WP_029386450.1|5033302_5034220_-|ABC-transporter-permease
MSQVLHTPPPTTAPPATDLAALAARHGLSVSGARPSLPRYVRQLWARRHFITAFATAKLTAQYSQAKLGQVWQVMTPLLNAAVYYFIFGLLLQTKQGVPDYVPFLVTGVFIWTFTQSSVMAGTRAISGNLGLVRALHFPRAALPLSFCLQQLQQLLFSMAALVVILLAFGVPPAPSWLLAVPALVLQFVFNAGLSMAMARLGAKTPDIAQLMPFVLRTWMYASGVMWSIDHMTSDRSGLPSWVGPLLQANPAAVYIDLMRFALIDTFHASQLPPHVWAIATGWALLAGVGGFVYFWKAEEMYGRG

Crispr_ID: NZ_LN831790_11

• CRISPR_ID: NZ_LN831790_11
• CRISPR_location: 5459686-5459833
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_LN831790_11

Consensus_repeat	Method
CCGCCACCGAGCCGGCCGCCGAG	CRISPRCasFinder

spacers of NZ_LN831790_11

>11.1|5459709|22|NZ_LN831790|CRISPRCasFinder
CCCGCCGCCGTCGAGGACGCCG
>11.2|5459754|19|NZ_LN831790|CRISPRCasFinder
GCTCCGGCCGCCGAGGCAG
>11.3|5459796|14|NZ_LN831790|CRISPRCasFinder
CCCAAGGGCCGCAC

CRISPR arrays and Neighbor proteins around NZ_LN831790_11

CRISPR arrays

The CRISPR arrays of NZ_LN831790_11

>merge|NZ_LN831790|11|5459686-5459833|CRISPRCasFinder
CGGCCGCCGAGGCGCTGGCCGAGCCCGCCGCCGTCGAGGACGCCGTCGTCGCGGCGCCGGCCCCCGAGGCTCCGGCCGCCGAGGCAGCGGTCACCGAGGAGGAGGCCGCGCCCAAGGGCCGCACCCGTCGCCGGGCGACCCGCCGGGC

>NZ_LN831790|11|11|5459686-5459833|CRISPRCasFinder
CGGCCGCCGAGGCGCTGGCCGAG	CCCGCCGCCGTCGAGGACGCCG
TCGTCGCGGCGCCGGCCCCCGAG	GCTCCGGCCGCCGAGGCAG
CGGTCACCGAGGAGGAGGCCGCG	CCCAAGGGCCGCAC
CCGTCGCCGGGCGACCCGCCGGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	unknown	unknown	gnl|CDD|133014
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	unknown	unknown	gnl|CDD|274574
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	unknown	unknown	gnl|CDD|340847
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	unknown	unknown	gnl|CDD|379420
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	unknown	unknown	gnl|CDD|235460
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	unknown	unknown	gnl|CDD|237560
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2	unknown	unknown	gnl|CDD|274573
NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl|CDD|224012
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	unknown	unknown	gnl|CDD|235510
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	unknown	unknown	gnl|CDD|188475
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	unknown	unknown	gnl|CDD|179085
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	unknown	unknown	gnl|CDD|223362
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	unknown	unknown	gnl|CDD|237562
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	unknown	unknown	gnl|CDD|378393
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	unknown	unknown	gnl|CDD|237045
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	unknown	unknown	gnl|CDD|235464
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|341453

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	gnl|CDD|133014	cd02523, PC_cytidylyltransferase, Phosphocholine cytidylyltransferases catalyze the synthesis of CDP-choline. This family contains proteins similar to prokaryotic phosphocholine (P-cho) cytidylyltransferases. Phosphocholine (PC) cytidylyltransferases catalyze the transfer of a cytidine monophosphate from CTP to phosphocholine to form CDP-choline. PC is the most abundant phospholipid in eukaryotic membranes and it is also important in prokaryotic membranes. For pathogenic prokaryotes, the cell surface PC facilitates the interaction with host surface and induces attachment and invasion. In addition cell wall PC serves as scaffold for a group of choline-binding proteins that are secreted from the cells. Phosphocholine (PC) cytidylyltransferase is a key enzyme in the prokaryotic choline metabolism pathway. It has been hypothesized to consist of a choline transport system, a choline kinase, CTP:phosphocholine cytidylyltransferase, and a choline phosphotransferase that transfers P-Cho from CDP-Cho to either lipoteichoic acid or lipopolysaccharide.	1.88115e-61
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	gnl|CDD|274574	TIGR03426, shape_MreD, rod shape-determining protein MreD. Members of this protein family are the MreD protein of bacterial cell shape determination. Most rod-shaped bacteria depend on MreB and RodA to achieve either a rod shape or some other non-spherical morphology such as coil or stalk formation. MreD is encoded in an operon with MreB, and often with RodA and PBP-2 as well. It is highly hydrophobic (therefore somewhat low-complexity) and highly divergent, and therefore sometimes tricky to discover by homology, but this model finds most examples. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	7.73759e-15
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	gnl|CDD|340847	cd03820, GT4_AmsD-like, amylovoran biosynthesis glycosyltransferase AmsD and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. AmSD in Erwinia amylovora has been shown to be involved in the biosynthesis of amylovoran, the acidic exopolysaccharide acting as a virulence factor. This enzyme may be responsible for the formation of galactose alpha-1,6 linkages in amylovoran.	1.01466e-84
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	gnl|CDD|379420	pfam14017, DUF4233, Protein of unknown function (DUF4233). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 122 and 147 amino acids in length. Proteins in this family are integral membrane proteins.	9.09264e-23
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	gnl|CDD|235460	PRK05429, PRK05429, gamma-glutamyl kinase; Provisional.	0
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	gnl|CDD|237560	PRK13922, PRK13922, rod shape-determining protein MreC; Provisional.	5.32001e-68
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|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_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.96151e-110
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	gnl|CDD|224012	COG1087, GalE, UDP-glucose 4-epimerase [Cell envelope biogenesis, outer membrane].	7.07431e-136
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	gnl|CDD|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	1.58441e-39
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	gnl|CDD|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	0
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	gnl|CDD|179085	PRK00668, ndk, mulitfunctional nucleoside diphosphate kinase/apyrimidinic endonuclease/3'-; Validated.	2.06794e-76
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	6.06473e-155
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	gnl|CDD|223362	COG0285, FolC, Folylpolyglutamate synthase [Coenzyme metabolism].	6.7133e-138
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	gnl|CDD|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	gnl|CDD|378393	pfam10105, DUF2344, Uncharacterized protein conserved in bacteria (DUF2344). This domain, found in various hypothetical bacterial proteins and Radical Sam domain proteins, has no known function. This domain is distantly related to tRNA pseudouridine synthases, suggesting this family may carry out a function related to RNA modification. But this family appears to lack the catalytic aspartate found in pseudouridine synthases.	1.62633e-69
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	gnl|CDD|237045	PRK12296, obgE, GTPase CgtA; Reviewed.	0
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|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].	3.40526e-128
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	gnl|CDD|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	3.49902e-46
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	gnl|CDD|341453	cd08174, G1PDH-like, Glycerol-1-phosphate dehydrogenase-like. These glycerol-1-phosphate dehydrogenase-like proteins have not been characterized. The protein sequences have high similarity with that of glycerol-1-phosphate dehydrogenase (G1PDH) which plays a role in the synthesis of phosphoglycerolipids in Gram-positive bacterial species. It catalyzes the reversibly reduction of dihydroxyacetone phosphate (DHAP) to glycerol-1-phosphate (G1P) in a NADH-dependent manner. Its activity requires Ni++ ion.	1.50094e-144

Protein sequences

>NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein
MQRIRLRYTKRGRLRFTSHRDFQRAFERALRRAEVPMAYSAGFTPHPKVSYANAAPTGTGSEAEYLEIALTEPRDPEQLRALLDESLPAGLDVVEAVEARTSGLADRLTASVWELRLDGVEPAEAARAVEAFNAAGAVEVQRLTKNGVRTFDARPAVASLESVETHGSPADRPSDRPCAILRLVVRHVTPAVRPDDVLSGLRAVADLAPPVPAAVTRLAQGLFDEETGTVTDPLAPDREAAANEPQTADATAAAKAPA
>NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein
MPAEAAESVFPQLEALLPHVQKPIQYVGGELNSTVKDWDSCDVRWALMYPDAYEVGLPNQGVMILYEVLNEQEGVLAERTYSVWPDLEALMREHGVPQFTVDSHRPVRAFDVFGLSFSTELGYTNMLAALELAGIPLEARDRGLDDPIVMAGGHAAFNPEPIADFIDCAIIGDGEQAVLEVTALIRAWKAEGRPGGREELLLRLAKTGGVYVPGFYDVEYLPDGRIARVVPNRSGVPWRVSKHTVMDLDEWPYPKQPLVPLAETVHERMSVEIFRGCTRGCRFCQAGMITRPVRERSITGIGEMVEKGLNATGFEEVGLLSLSSADHSEIGDIAKGLADRYADDKIGLSLPSTRVDAFNIDLANELTRNGRRSGLTFAPEGGSERIRKVINKMVSEEDLIRTVATAYGNGWRQVKLYFMCGLPTETDEDVLQIADMATRVIQKGREVSGSNDIRCTVSIGGFVPKPHTPFQWAPQLSAEETDARLAKLRDKIRGDKKYGRSIGFRYHDGKPGIVEGLLSRGDRRIGAVIRAVYEDGGRFDGWREHFSYDRWMSCAEKALAPFGVDVDWYTTRERGYEEVLPWDHLDSGLDKDWLWEDWQDALDETEVEDCRWTPCFDCGVCPQMDTHIQIGPTGKKLLPLTVKNAAPSAG
>NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA
MTGANGFQVSGYGPERAGWTRVFARDSVARRLDWPILLSATALSLIGAVLVYSATRNRTELNQGDPYFFLVRHLLNTGIGIALMIATVWLGHRTLRTAVPLLYGASVFLILLVLTPLGSTVNGAHSWIQLGGGFSVQPSEFVKVTIILGMAMLLAARVDAGDKPYPDHRTVIQALALATVPMLIVMLMPDLGSVMVMVVIVLGVLLASGASNRWVFGLLGAGAVGAVAVWQLGILDEYQINRFAAFANPELDPAGVGYNTNQARIAIGSGGLTGSGLFHGSQTTGQFVPEQQTDFVFTVAGEELGFLGAGFIILLLGVVLWRACRIARETSDLYGTIVAAGIVAWFAFQAFENIGMTLGIMPVTGLPLPFVSYGGSSMFAVWIAVGLLQSITVQRPMSA
>NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2
MTNIPETGRSPRVQIRLVVIQVLVLSLLGTLGGRLWYLQIREGDEYAEKASGNHVQQVVQPAVRGSILDARGVPLADNETRLVVSASRTDLMKMEDDGKAVLTKLAGVLGMRPQEVMEKVRLCDAETPQPCWNGSPYQPIPITDEATPKQALQIRERAEDFPGITAEPQAVRRYPSPGEANTAQVLGYLSPVTDEEIKQAQDSESPYLRSDQVGRSGLERQYDKQLRGKAGVTRYEVDNLGRVIGKAESDAAQPGSNLVTSIDARVQRIAEYELNEAMKAARKEYDRNTGTTYKADSGAVVVMEARTGRVVAMASNPTYDPNAWVGGISSADYQKLTGKNSNYPLLNRAIQGQAAPGSIFKVVSTAAAVEAGYDFDGSYQCSSAYSVGGQVFKNFESANYGAIDLGRALEVSCDTVYYRLAHQEWKKDGGINPKGRPKDHFFKAAHQFGLGKETGIDLPNEVSGRVPDREWKQRYWEANKDAWCKTGKKDGSYVEKIAYENCVEGNKMRAGDEINYSIGQGDTLVTPIQMATIYAAISNGGTLYTPSIGKAIVSPDGKKVSEIEPEPHGRLPISDATRDKMDAALAGVATRGTAAWRFGGWPQDEIPMHAKTGTAEVYGKQTTSWFATYTDDYAIVMTISQGGTGSGASGPAVRKIYDALYGVQEDGSIDRKKALLPEPAKSLPEIKPDGTITAPKTAEDPVKRDRATEQDENAPADTGQPQDDAATVATPAAENRQTRRRRRGGGRGGTTGTGTAARAGTRSRRRCA
>NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD
MRVNRILLSVSLVVVALVIQVSVLARLHLPGAVPDLLLLTVLGLALVYGHVGGALVGFGAGLLADLAPPADHAAGRYALVLCVVGYLAGLVKPENGRLKSAAGPMAVVVAAAVASTLLYAGVGALVGDTAARHVGLPGLLFTAALYDLLLAPFVVPGIMALARRAENDPLAETSSTAQTTDISSGWVAGGTGLRIGGQRNGLRVKAARARVARAGRIKGVKRL
>NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC
MRDTKESRLLLVLLIAIAFALITVDIRGGEDSPVDGARHAAATVFGPIENGVSAAVDPVGNAVAAIRDSGRRHDRLAELEKENAALKAKLGSDDRGRSRLKQLDSMLKIAGKGQYGIKGAQVIAIGAAQGFSWTITIDVGANDGIKRDMTVLNGDGLVGRVTTVGPETATVLLASDPDFTVGTRLEGSDELGFASGQGDRPLRVELLNGKAEVKKGDRLVTFGSQADKPFVPGVPVGVVSRVDPSGGGLTRTLYVTPYVGFTKLDIVGVVVQAPRKDPRDTVLPAEPRPVPTPTVTVTVTPSAEAPADGQYPSEQPEQ
>NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein
MSFIGRDMAVDLGTANTLVYVRGRGIVLNEPSVVAINTNTGGILAVGAEAKKMIGRTPGNIVAVRPLKDGVIADFEITERMLRYFILKIHKRRYLARPRVVVCVPSGITGVERRAVIEASSQAGARQVHIIEEPMAAAIGSGLPVHEATGNMVVDIGGGTTEVAVISLGGIVTAQSIRVAGDELDNAIIQHVKKEYSLLLGERTAEQIKITIGSAYDLDTDEHTEIRGRDLVSGLPKTVVISAAEVRKAIEEPVNAIVDAVKTTLDKCPPELSGDIMDRGIVLTGGGALLRGLDERLRRETGMPIHIAEDPLDSVALGSGKCVEEFEALQQVLDAQPRR
>NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase
MTQRTLVLLKPDAVRRGLTGEIISRIERKAGWQITALELRTLDAETLEQHYGEHKGKPFYEPLVEFMASGPVVAMIVEGERVIEGVRQLAGPTDPIAAPAGSIRGDYGVIVRENLIHASDSEESAERELKIFFPGRV
>NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein
MRTLCSSTLIGEFFVIAFAGLVAMKDPDLSMAAVWTVSGIAMFLCLVLCGLVTRPGGIALGWALQIALVAAGFVVPTMFFMGAVFAALWWASVHYGRKIDEAKARFAAQAGTQAPDAV
>NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase
MSELPPHDSSEQPDPAGSFDEIIEAETERDPDLAVIEAGSRTLRTQGGPPQADVPARPEDPEVDKALREVEAELATRWGETKLEPSVSRIAALMDVLGEPQRSYPSIHITGTNGKTSTARMIEALLGAFDLRTGRYTSPHVQSITERISLDGAPISAERFIETYQDVKPYVEMVDGRQEYRLSFFEVLTGMAYAAFADAPVDVAVVEVGMGGSWDATNVIDGDVAVVTPIDLDHTDRLGSTTAEIATEKAGIIKQDATVILAQQPVDAAQALLKKAVDVGATVAREGLEFGVVARQVAVGGQLLTLRGLGGEYTEVYLPLHGAHQAHNAAVALAAVEAFFGVGAQRAETLDIDTVRKAFAAVSSPGRLEVVRRSPTVVLDAAHNPAGARVTADAIGEAFQFSRLIGVVGASADKDVRGLLEAFEPVFAEVVVTQNSSHRAMDADALAAVAVEVFGEERVQVEPRLPDALEAAITLAEEEGEFAGGGVLVTGSVITVGEARLLLGRG
>NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein
MIGLILAAGAGRRLRPYTDTLPKALVPVGPEGAEDSLTVLDLTLGNFAEVGLTEAAIIVGYRKEAVYARKEALEAKYGLKLTLIDNDKAEEWNNAYSLWCGREALKDGVILANGDTVHPVSVEKTLLAARGDGKKIILALDTVKQLAEEEMKVVVDPAKGVRRITKLMDPAEATGEYIGVTLIEGEAAAELADALKATFERDPQLYYEDGYQELVDRGFTVDVAPIGDVRWVEIDNHDDLAKGREIACRY
>NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein
MPLLTRLIPAPVVVDIRAGALDDLTSVLADQRISQSGRLAVAVSGGSGARLRERLAPALPGAEWFEVGGGTIDDAVRLADAMKGGRYDAVVGLGGGKVIDCAKYSAARVGLPMVAVATNLSHDGICSPVSILDNDAGRGSYGVPTPIAILVDLAVIREAPIRFVRSGIGDAVSNISAVADWELAHRVNGEKVDGLAAAMARQAGEAVLRHPGGCGDDGFLTVLTEGLVLSGIAMSIAGHTRPSSGACHEISHALDLLYPRRAASHGEQVGLGAAFAMHLRGDHEGSRLMAGVLRRHGLPVLAEEIGFDDDEFVRAVEFAPQTRPGRYTILEHLELSPARIREAYADYAASVDD
>NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21
MYAIVRSGGRQHKVAVGDIVEVDKISTAKVGDTVELSTLLVVDGDSVTSDPWVLAGIKVQAEVVDHHKGQKIDILRYKNKTGYRRRQGHRQQYTAIKVTEIPTAAK
>NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27
MAHKKGASSTRNGRDSNAQRLGVKRFGGQVVNAGEILVRQRGTHFHPGSGVGRGGDDTLFALQAGSVQFGTHRGRKVVNIVPVA
>NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE
MTTFVDRVELHVAAGNGGHGCASVHREKFKPLGGPDGGNGGRGGDVILTVDQSVTTLLEYHHSPHRKATNGKPGEGGHRSGKDGQDLVLAVPDGTVVLDKAGNVLADLVGHGTSYVAAQGGRGGLGNAALASARRKAPGFALLGEPGDVCEIVLELKTVADVALVGYPSAGKSSLISVLSAAKPKIADYPFTTLVPNLGVVTAGSTVYTIADVPGLIPGASQGKGLGLEFLRHVERCSVLVHVLDTATLESDRDPVSDLDVIEEELRQYGGLDNRPRLVVLNKIDVPDGRDLAEMVRPDLQARGYRVFEVSAVAHTGLKELSFALAELVAAARAARPKEEATRIVIRPKAVDDAGFTVTREEDGLFRVRGEKPERWVRQTDFNNDEAVGYLADRLNRLGVEEELMKAGARAGDGVAIGPEENAVVFDWEPSVMAGAEMLGRRGEDHRLEAPRPAAQRRRDRQAERDDAQREFDDFEPF
>NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase
MGGVVSATQNLAGALADRHEVEIVALRKVRDESYFPLDPRVSVRVLSDLRPHSPVSDLDDPLVEKWPLVYPPNTGAKKPVVSRLAERRLLEYLATTDADVVVSSSPRNTIMLAQAPGTYLKVAQEHSMPSIYAKDIKERLFPAYLSLDALTALTPEEVESIGRQVPAVRDRLAVMPNCVPASPIRSKGTNKVVVCAGHLTDNKNHALLVEAFAKVHAQAPDWTLRIYGSGAEKARLRARIEELGLSNSILLMGQTAPVTPEFGKGSIFVLPSKREAFGNVIVEAMAAGLPVVSTDADHGPRNILTPGEDGLLVPRGDVEEMARAILRLVQDDELRQKMAANAVRGAERFHETASRERFEAILERALARKALPRHATARVDDRGSVHIEVGPLPERARGAELVLRRSGKNGEEHRFPLSDSGEALVAWDAGLPHGTWEAALASPSGGEVPLTTDGYGCDTRDLLAVELPRPHGHPLALLLPHRHDDGRLRVRSALRAVHAEVGPVRVDDQAVRLRAELWGATLGRGAVVEAVHRRDKERVLTFEARDAGDGAFEAVVDCAALAREHGEEDGKEAIWDFWIRPEEGAPRAALAKLATDVLKPIDVFTFPRPVLTSGAVARPSVVRRAARRARRSLGATPAALPRPVRTELRPYYTALSQFAVKTVRL
>NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MAPRLSVIVPIYDVERYLPACLDSLAAQTFRDFEVLMVDDGSPDDSASIAAAYAERDPRFKLIRKENGGLGAARNTGIAHMSPQAEYVTFVDSDDLIPPDAYRLMVSSLDESGSDFATGNVFHLKGEKTWQVPLLRMLAGEARRATHISRYGKLVADRIACNKVFRRTFWEKHGFAFPEGRLYEDTPVTMRAHYLADAVDVISEPCYYWRLREGESAPSITQRRTDPAGVRDRVTSVLEISAFLAEQPGEMFARLKEEYDTRVLKDDLRLFLNVVPDGDEEYRAEFLRSANRFLDRIDPKVVMALPAQLRVQWLLVRKHKLDELITLLAGQRRKEAVEVSGLVRKYASFPSLADADLDFPRKALRIDQDLRMRAPLQEVTWSEGKLVLSGNAWIDKIDLASKHSSVKVLQLRKDKSRRRILLPARNIHRPECTTNSGQDRYNYDWAGWEVTIDPARLRKGGEWQEGLWHVGLGLYASGLVRRAAVQSSGGAACNFPPYHWLSPDFRLLPSVERGALKIRIERVRALITGRTVEGDRIVVTGEIRVPLAAGENVVLRVRNQKGADVHEYPVTVTDEGGTHRFSVEVPVADVALVFHDGVDAKAQPENRTWSTALIARDPQGAERQFSTVLQEGLPDARFNLPASLGERAELCELAIVAGHTGYLKFAGRTRRATIDRVGVEDGRITIAAHTDPRLTGARFLLKPRNRFEERFVEARWSEDGRFEVAFDPSTLGGGGNVPLRAGRWNLWLRPEDGAPDVPFVTDRLAADQFPLRAELNGRRYWLENRWADFPQLNCRSELSDLERGPFRQKQLRRDLYQPLRRQPLRDQVFYLSYNGKQFSDSPKAMYQELVRRGSDLKHLWAVRDGQVILPEGVEPVRMWGTEWYEALATSRYIVTNGHLPDWIERRPGQVIVQTWHGTMLKKIGHDIDTLHFDRRYQEKLALEAKQWSLVVSSNRFSTPILKRAFSYDGEILEAGYPRNDYLYSPDKDRIAERVKKQLGLPEGKKVVLYAPTWRDDLSHSAGQYLFDLRIDLEDAQRRLGDDHVLLIRRHSNVVDAVPGAGNGFVWDVSEYPDIADLYLAADVMITDYSSVMFDYAHLRRPMLFFTYDLEHYRDTLRGFYFDFEQDSPGPLIATSKELVDALRDIDQVSAEYQERFERFHHLFCDLDDGNASTRVVDRMLEQSREL
>NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MPKLSLVVPVYKVQGYLPECLDSVLGQDYTDFEIIAVDDCSPDGSGAILDEYARRDARIHVIHLTENVGLGRARNAGLEKAQGEYVLFLDSDDTLSDGALTAISERLAATGDPEILVFDYARTYWDGQVRPNQRADLLKSDGPEVFRLAERPQLLDLLQIVWNKAYRRDFITRTGLTFPPGYYEDAPWTFCSLISAERIAVLDRVCVLYRQRREGGNILKTVSRKHFDVFDQYRRVFDFLDAHEELDRWRGPLFRKMVDHYLTVLERPGRLPREARAEFFHRASADYRARLPKGFQKPAGGRGHKYAMLERDAYAAMMSASTAVKLRRTVRKRTRDALNRSKRSAMGVHYQSQLRLPLDENLVLFSAYWSRSVSCNPAAIDAELARLAPHLRRVWAIRPDAVDQVPKGVEYVRVGSRAYWTALARAKYLVNNVNFADAVVKREGQIHLQTHHGTPLKTMGLDQQKYPASTDMNFEKLLERCDRWDYSISSNRFSTAIWERVYPCSYVSLETGYPRNDVLVNAGAEEVRRARAALGLADGAKAFLYMPTHREYQPGFTPSLDLARLAEELGPDVTLLLRGHYFYGSSPHIAELRRSGRIVDVSGHPRVEELYLAADALITDYSSAMFDYAVLDRPIIVYAPDWDIYSAVRGTYFDLLQEPPGAVATSQAELIRLLGSGDYDSRDAAGRRDAFRRRFCEFDDGHAAERVVRRVFLGDQTPLPFVPFDERSHAPTPAQALEPVERA
>NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE
MSWLVTGGAGYIGAHVVRAMAAGGERVVVYDDLSTGSADRVPDGVPLVVGSVLDASLLARAIRDHAVTGVVHIAAKKQVGESVEQPLRYYRENVTGLRTLLEVMTDAGVGKLVFSSSAAVYGMPDVELVTEDTPCAPMSPYGETKLVGEWLIAATARAHGIRAASLRYFNVAGAAEPALADAGVFNLIPMVFERLEAGEAPRIFGDDYATPDGTCVRDYIHVEDIASAHLAAARRLGEAAEGTNLVLNIGRGEGSSVREMVDRILKITGHEHLTPAVAERRPGDPARVVASADRIRRELDWSAHHDLDDMIRSAWQGWRHLRG
>NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase
MGEARRIVVKVGSSSLTTAEGGLDADRVDALVDVLAKVRSGGEREIVLVSSGAIAAGLAPLGLRRRPRDLARQQAAASVGQGLLVARYTASFARYGVRVGQVLLTSDDMSRRAHHRNASRTLDKLLAMGAFPIVNENDTVATDEIRFGDNDRLAALVAHLVHADLLVLLSDVDGVYDGDPGRPGTARIAEVRRPEDLAHVEIGSAGKAGVGTGGMVTKVEAARIAAAAGIPVVLTSAVHAADALTGQDTGTYFHPTGKRSADRLLWLQHASTPQGALTLDDGAVRAVVEGRKSLLPAGIAAVEGEFVAGDPVELRDGEGRAVARGLVSFDAKEIPRLIGRSTRELARELGPAYEREVVHRDDLVILHP

Crispr_ID: NZ_LN831790_12

• CRISPR_ID: NZ_LN831790_12
• CRISPR_location: 5459968-5460231
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_LN831790_12

Consensus_repeat	Method
CCGCCACCGAGCCGGCCGCCGAG	CRISPRCasFinder

spacers of NZ_LN831790_12

>12.1|5459991|43|NZ_LN831790|CRISPRCasFinder
GCCCGTCCGCGGCGCCGCGCCGTGCGGAAGGCCGCCGCGCCGA
>12.2|5460057|25|NZ_LN831790|CRISPRCasFinder
GTGGTCCTCCCGGCCGCCACCGAGC
>12.3|5460105|43|NZ_LN831790|CRISPRCasFinder
GCCCAGGAGGCTCCGGTTCAGGAGGCCGCGGCTTCGGAGGCTC
>12.4|5460171|37|NZ_LN831790|CRISPRCasFinder
GGCCCGGAAGCAGCCGAGGCCGCGGCTTCGGAGGCTC

CRISPR arrays and Neighbor proteins around NZ_LN831790_12

CRISPR arrays

The CRISPR arrays of NZ_LN831790_12

>merge|NZ_LN831790|12|5459968-5460231|CRISPRCasFinder
CCGCCGCCGAGCCGGCCGCGCCGGCCCGTCCGCGGCGCCGCGCCGTGCGGAAGGCCGCCGCGCCGACCGCGCCCGCGGAGGCCGCCGTCGTGGTCCTCCCGGCCGCCACCGAGCCGGCCGCCGAGCCGGAAGCCCCGGCCCAGGAGGCTCCGGTTCAGGAGGCCGCGGCTTCGGAGGCTCCCGCCGCCGAGCCGGCCGCCGAGGGCCCGGAAGCAGCCGAGGCCGCGGCTTCGGAGGCTCCCGCCGCCGAGCCGGCCGCCGAGG

>NZ_LN831790|12|12|5459968-5460231|CRISPRCasFinder
CCGCCGCCGAGCCGGCCGCGCCG	GCCCGTCCGCGGCGCCGCGCCGTGCGGAAGGCCGCCGCGCCGA
CCGCGCCCGCGGAGGCCGCCGTC	GTGGTCCTCCCGGCCGCCACCGAGC
CGGCCGCCGAGCCGGAAGCCCCG	GCCCAGGAGGCTCCGGTTCAGGAGGCCGCGGCTTCGGAGGCTC
CCGCCGCCGAGCCGGCCGCCGAG	GGCCCGGAAGCAGCCGAGGCCGCGGCTTCGGAGGCTC
CCGCCGCCGAGCCGGCCGCCGAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	unknown	unknown	gnl|CDD|133014
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	unknown	unknown	gnl|CDD|274574
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	unknown	unknown	gnl|CDD|340847
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	unknown	unknown	gnl|CDD|379420
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	unknown	unknown	gnl|CDD|235460
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	unknown	unknown	gnl|CDD|237560
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2	unknown	unknown	gnl|CDD|274573
NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl|CDD|224012
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	unknown	unknown	gnl|CDD|235510
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	unknown	unknown	gnl|CDD|188475
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	unknown	unknown	gnl|CDD|179085
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	unknown	unknown	gnl|CDD|223362
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	unknown	unknown	gnl|CDD|237562
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	unknown	unknown	gnl|CDD|378393
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	unknown	unknown	gnl|CDD|237045
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	unknown	unknown	gnl|CDD|235464
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|341453

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	gnl|CDD|133014	cd02523, PC_cytidylyltransferase, Phosphocholine cytidylyltransferases catalyze the synthesis of CDP-choline. This family contains proteins similar to prokaryotic phosphocholine (P-cho) cytidylyltransferases. Phosphocholine (PC) cytidylyltransferases catalyze the transfer of a cytidine monophosphate from CTP to phosphocholine to form CDP-choline. PC is the most abundant phospholipid in eukaryotic membranes and it is also important in prokaryotic membranes. For pathogenic prokaryotes, the cell surface PC facilitates the interaction with host surface and induces attachment and invasion. In addition cell wall PC serves as scaffold for a group of choline-binding proteins that are secreted from the cells. Phosphocholine (PC) cytidylyltransferase is a key enzyme in the prokaryotic choline metabolism pathway. It has been hypothesized to consist of a choline transport system, a choline kinase, CTP:phosphocholine cytidylyltransferase, and a choline phosphotransferase that transfers P-Cho from CDP-Cho to either lipoteichoic acid or lipopolysaccharide.	1.88115e-61
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	gnl|CDD|274574	TIGR03426, shape_MreD, rod shape-determining protein MreD. Members of this protein family are the MreD protein of bacterial cell shape determination. Most rod-shaped bacteria depend on MreB and RodA to achieve either a rod shape or some other non-spherical morphology such as coil or stalk formation. MreD is encoded in an operon with MreB, and often with RodA and PBP-2 as well. It is highly hydrophobic (therefore somewhat low-complexity) and highly divergent, and therefore sometimes tricky to discover by homology, but this model finds most examples. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	7.73759e-15
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	gnl|CDD|340847	cd03820, GT4_AmsD-like, amylovoran biosynthesis glycosyltransferase AmsD and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. AmSD in Erwinia amylovora has been shown to be involved in the biosynthesis of amylovoran, the acidic exopolysaccharide acting as a virulence factor. This enzyme may be responsible for the formation of galactose alpha-1,6 linkages in amylovoran.	1.01466e-84
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	gnl|CDD|379420	pfam14017, DUF4233, Protein of unknown function (DUF4233). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 122 and 147 amino acids in length. Proteins in this family are integral membrane proteins.	9.09264e-23
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	gnl|CDD|235460	PRK05429, PRK05429, gamma-glutamyl kinase; Provisional.	0
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	gnl|CDD|237560	PRK13922, PRK13922, rod shape-determining protein MreC; Provisional.	5.32001e-68
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|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_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.96151e-110
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	gnl|CDD|224012	COG1087, GalE, UDP-glucose 4-epimerase [Cell envelope biogenesis, outer membrane].	7.07431e-136
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	gnl|CDD|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	1.58441e-39
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	gnl|CDD|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	0
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	gnl|CDD|179085	PRK00668, ndk, mulitfunctional nucleoside diphosphate kinase/apyrimidinic endonuclease/3'-; Validated.	2.06794e-76
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	6.06473e-155
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	gnl|CDD|223362	COG0285, FolC, Folylpolyglutamate synthase [Coenzyme metabolism].	6.7133e-138
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	gnl|CDD|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	gnl|CDD|378393	pfam10105, DUF2344, Uncharacterized protein conserved in bacteria (DUF2344). This domain, found in various hypothetical bacterial proteins and Radical Sam domain proteins, has no known function. This domain is distantly related to tRNA pseudouridine synthases, suggesting this family may carry out a function related to RNA modification. But this family appears to lack the catalytic aspartate found in pseudouridine synthases.	1.62633e-69
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	gnl|CDD|237045	PRK12296, obgE, GTPase CgtA; Reviewed.	0
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|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].	3.40526e-128
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	gnl|CDD|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	3.49902e-46
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	gnl|CDD|341453	cd08174, G1PDH-like, Glycerol-1-phosphate dehydrogenase-like. These glycerol-1-phosphate dehydrogenase-like proteins have not been characterized. The protein sequences have high similarity with that of glycerol-1-phosphate dehydrogenase (G1PDH) which plays a role in the synthesis of phosphoglycerolipids in Gram-positive bacterial species. It catalyzes the reversibly reduction of dihydroxyacetone phosphate (DHAP) to glycerol-1-phosphate (G1P) in a NADH-dependent manner. Its activity requires Ni++ ion.	1.50094e-144

Protein sequences

>NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein
MQRIRLRYTKRGRLRFTSHRDFQRAFERALRRAEVPMAYSAGFTPHPKVSYANAAPTGTGSEAEYLEIALTEPRDPEQLRALLDESLPAGLDVVEAVEARTSGLADRLTASVWELRLDGVEPAEAARAVEAFNAAGAVEVQRLTKNGVRTFDARPAVASLESVETHGSPADRPSDRPCAILRLVVRHVTPAVRPDDVLSGLRAVADLAPPVPAAVTRLAQGLFDEETGTVTDPLAPDREAAANEPQTADATAAAKAPA
>NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein
MPAEAAESVFPQLEALLPHVQKPIQYVGGELNSTVKDWDSCDVRWALMYPDAYEVGLPNQGVMILYEVLNEQEGVLAERTYSVWPDLEALMREHGVPQFTVDSHRPVRAFDVFGLSFSTELGYTNMLAALELAGIPLEARDRGLDDPIVMAGGHAAFNPEPIADFIDCAIIGDGEQAVLEVTALIRAWKAEGRPGGREELLLRLAKTGGVYVPGFYDVEYLPDGRIARVVPNRSGVPWRVSKHTVMDLDEWPYPKQPLVPLAETVHERMSVEIFRGCTRGCRFCQAGMITRPVRERSITGIGEMVEKGLNATGFEEVGLLSLSSADHSEIGDIAKGLADRYADDKIGLSLPSTRVDAFNIDLANELTRNGRRSGLTFAPEGGSERIRKVINKMVSEEDLIRTVATAYGNGWRQVKLYFMCGLPTETDEDVLQIADMATRVIQKGREVSGSNDIRCTVSIGGFVPKPHTPFQWAPQLSAEETDARLAKLRDKIRGDKKYGRSIGFRYHDGKPGIVEGLLSRGDRRIGAVIRAVYEDGGRFDGWREHFSYDRWMSCAEKALAPFGVDVDWYTTRERGYEEVLPWDHLDSGLDKDWLWEDWQDALDETEVEDCRWTPCFDCGVCPQMDTHIQIGPTGKKLLPLTVKNAAPSAG
>NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA
MTGANGFQVSGYGPERAGWTRVFARDSVARRLDWPILLSATALSLIGAVLVYSATRNRTELNQGDPYFFLVRHLLNTGIGIALMIATVWLGHRTLRTAVPLLYGASVFLILLVLTPLGSTVNGAHSWIQLGGGFSVQPSEFVKVTIILGMAMLLAARVDAGDKPYPDHRTVIQALALATVPMLIVMLMPDLGSVMVMVVIVLGVLLASGASNRWVFGLLGAGAVGAVAVWQLGILDEYQINRFAAFANPELDPAGVGYNTNQARIAIGSGGLTGSGLFHGSQTTGQFVPEQQTDFVFTVAGEELGFLGAGFIILLLGVVLWRACRIARETSDLYGTIVAAGIVAWFAFQAFENIGMTLGIMPVTGLPLPFVSYGGSSMFAVWIAVGLLQSITVQRPMSA
>NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2
MTNIPETGRSPRVQIRLVVIQVLVLSLLGTLGGRLWYLQIREGDEYAEKASGNHVQQVVQPAVRGSILDARGVPLADNETRLVVSASRTDLMKMEDDGKAVLTKLAGVLGMRPQEVMEKVRLCDAETPQPCWNGSPYQPIPITDEATPKQALQIRERAEDFPGITAEPQAVRRYPSPGEANTAQVLGYLSPVTDEEIKQAQDSESPYLRSDQVGRSGLERQYDKQLRGKAGVTRYEVDNLGRVIGKAESDAAQPGSNLVTSIDARVQRIAEYELNEAMKAARKEYDRNTGTTYKADSGAVVVMEARTGRVVAMASNPTYDPNAWVGGISSADYQKLTGKNSNYPLLNRAIQGQAAPGSIFKVVSTAAAVEAGYDFDGSYQCSSAYSVGGQVFKNFESANYGAIDLGRALEVSCDTVYYRLAHQEWKKDGGINPKGRPKDHFFKAAHQFGLGKETGIDLPNEVSGRVPDREWKQRYWEANKDAWCKTGKKDGSYVEKIAYENCVEGNKMRAGDEINYSIGQGDTLVTPIQMATIYAAISNGGTLYTPSIGKAIVSPDGKKVSEIEPEPHGRLPISDATRDKMDAALAGVATRGTAAWRFGGWPQDEIPMHAKTGTAEVYGKQTTSWFATYTDDYAIVMTISQGGTGSGASGPAVRKIYDALYGVQEDGSIDRKKALLPEPAKSLPEIKPDGTITAPKTAEDPVKRDRATEQDENAPADTGQPQDDAATVATPAAENRQTRRRRRGGGRGGTTGTGTAARAGTRSRRRCA
>NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD
MRVNRILLSVSLVVVALVIQVSVLARLHLPGAVPDLLLLTVLGLALVYGHVGGALVGFGAGLLADLAPPADHAAGRYALVLCVVGYLAGLVKPENGRLKSAAGPMAVVVAAAVASTLLYAGVGALVGDTAARHVGLPGLLFTAALYDLLLAPFVVPGIMALARRAENDPLAETSSTAQTTDISSGWVAGGTGLRIGGQRNGLRVKAARARVARAGRIKGVKRL
>NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC
MRDTKESRLLLVLLIAIAFALITVDIRGGEDSPVDGARHAAATVFGPIENGVSAAVDPVGNAVAAIRDSGRRHDRLAELEKENAALKAKLGSDDRGRSRLKQLDSMLKIAGKGQYGIKGAQVIAIGAAQGFSWTITIDVGANDGIKRDMTVLNGDGLVGRVTTVGPETATVLLASDPDFTVGTRLEGSDELGFASGQGDRPLRVELLNGKAEVKKGDRLVTFGSQADKPFVPGVPVGVVSRVDPSGGGLTRTLYVTPYVGFTKLDIVGVVVQAPRKDPRDTVLPAEPRPVPTPTVTVTVTPSAEAPADGQYPSEQPEQ
>NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein
MSFIGRDMAVDLGTANTLVYVRGRGIVLNEPSVVAINTNTGGILAVGAEAKKMIGRTPGNIVAVRPLKDGVIADFEITERMLRYFILKIHKRRYLARPRVVVCVPSGITGVERRAVIEASSQAGARQVHIIEEPMAAAIGSGLPVHEATGNMVVDIGGGTTEVAVISLGGIVTAQSIRVAGDELDNAIIQHVKKEYSLLLGERTAEQIKITIGSAYDLDTDEHTEIRGRDLVSGLPKTVVISAAEVRKAIEEPVNAIVDAVKTTLDKCPPELSGDIMDRGIVLTGGGALLRGLDERLRRETGMPIHIAEDPLDSVALGSGKCVEEFEALQQVLDAQPRR
>NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase
MTQRTLVLLKPDAVRRGLTGEIISRIERKAGWQITALELRTLDAETLEQHYGEHKGKPFYEPLVEFMASGPVVAMIVEGERVIEGVRQLAGPTDPIAAPAGSIRGDYGVIVRENLIHASDSEESAERELKIFFPGRV
>NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein
MRTLCSSTLIGEFFVIAFAGLVAMKDPDLSMAAVWTVSGIAMFLCLVLCGLVTRPGGIALGWALQIALVAAGFVVPTMFFMGAVFAALWWASVHYGRKIDEAKARFAAQAGTQAPDAV
>NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase
MSELPPHDSSEQPDPAGSFDEIIEAETERDPDLAVIEAGSRTLRTQGGPPQADVPARPEDPEVDKALREVEAELATRWGETKLEPSVSRIAALMDVLGEPQRSYPSIHITGTNGKTSTARMIEALLGAFDLRTGRYTSPHVQSITERISLDGAPISAERFIETYQDVKPYVEMVDGRQEYRLSFFEVLTGMAYAAFADAPVDVAVVEVGMGGSWDATNVIDGDVAVVTPIDLDHTDRLGSTTAEIATEKAGIIKQDATVILAQQPVDAAQALLKKAVDVGATVAREGLEFGVVARQVAVGGQLLTLRGLGGEYTEVYLPLHGAHQAHNAAVALAAVEAFFGVGAQRAETLDIDTVRKAFAAVSSPGRLEVVRRSPTVVLDAAHNPAGARVTADAIGEAFQFSRLIGVVGASADKDVRGLLEAFEPVFAEVVVTQNSSHRAMDADALAAVAVEVFGEERVQVEPRLPDALEAAITLAEEEGEFAGGGVLVTGSVITVGEARLLLGRG
>NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein
MIGLILAAGAGRRLRPYTDTLPKALVPVGPEGAEDSLTVLDLTLGNFAEVGLTEAAIIVGYRKEAVYARKEALEAKYGLKLTLIDNDKAEEWNNAYSLWCGREALKDGVILANGDTVHPVSVEKTLLAARGDGKKIILALDTVKQLAEEEMKVVVDPAKGVRRITKLMDPAEATGEYIGVTLIEGEAAAELADALKATFERDPQLYYEDGYQELVDRGFTVDVAPIGDVRWVEIDNHDDLAKGREIACRY
>NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein
MPLLTRLIPAPVVVDIRAGALDDLTSVLADQRISQSGRLAVAVSGGSGARLRERLAPALPGAEWFEVGGGTIDDAVRLADAMKGGRYDAVVGLGGGKVIDCAKYSAARVGLPMVAVATNLSHDGICSPVSILDNDAGRGSYGVPTPIAILVDLAVIREAPIRFVRSGIGDAVSNISAVADWELAHRVNGEKVDGLAAAMARQAGEAVLRHPGGCGDDGFLTVLTEGLVLSGIAMSIAGHTRPSSGACHEISHALDLLYPRRAASHGEQVGLGAAFAMHLRGDHEGSRLMAGVLRRHGLPVLAEEIGFDDDEFVRAVEFAPQTRPGRYTILEHLELSPARIREAYADYAASVDD
>NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21
MYAIVRSGGRQHKVAVGDIVEVDKISTAKVGDTVELSTLLVVDGDSVTSDPWVLAGIKVQAEVVDHHKGQKIDILRYKNKTGYRRRQGHRQQYTAIKVTEIPTAAK
>NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27
MAHKKGASSTRNGRDSNAQRLGVKRFGGQVVNAGEILVRQRGTHFHPGSGVGRGGDDTLFALQAGSVQFGTHRGRKVVNIVPVA
>NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE
MTTFVDRVELHVAAGNGGHGCASVHREKFKPLGGPDGGNGGRGGDVILTVDQSVTTLLEYHHSPHRKATNGKPGEGGHRSGKDGQDLVLAVPDGTVVLDKAGNVLADLVGHGTSYVAAQGGRGGLGNAALASARRKAPGFALLGEPGDVCEIVLELKTVADVALVGYPSAGKSSLISVLSAAKPKIADYPFTTLVPNLGVVTAGSTVYTIADVPGLIPGASQGKGLGLEFLRHVERCSVLVHVLDTATLESDRDPVSDLDVIEEELRQYGGLDNRPRLVVLNKIDVPDGRDLAEMVRPDLQARGYRVFEVSAVAHTGLKELSFALAELVAAARAARPKEEATRIVIRPKAVDDAGFTVTREEDGLFRVRGEKPERWVRQTDFNNDEAVGYLADRLNRLGVEEELMKAGARAGDGVAIGPEENAVVFDWEPSVMAGAEMLGRRGEDHRLEAPRPAAQRRRDRQAERDDAQREFDDFEPF
>NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase
MGGVVSATQNLAGALADRHEVEIVALRKVRDESYFPLDPRVSVRVLSDLRPHSPVSDLDDPLVEKWPLVYPPNTGAKKPVVSRLAERRLLEYLATTDADVVVSSSPRNTIMLAQAPGTYLKVAQEHSMPSIYAKDIKERLFPAYLSLDALTALTPEEVESIGRQVPAVRDRLAVMPNCVPASPIRSKGTNKVVVCAGHLTDNKNHALLVEAFAKVHAQAPDWTLRIYGSGAEKARLRARIEELGLSNSILLMGQTAPVTPEFGKGSIFVLPSKREAFGNVIVEAMAAGLPVVSTDADHGPRNILTPGEDGLLVPRGDVEEMARAILRLVQDDELRQKMAANAVRGAERFHETASRERFEAILERALARKALPRHATARVDDRGSVHIEVGPLPERARGAELVLRRSGKNGEEHRFPLSDSGEALVAWDAGLPHGTWEAALASPSGGEVPLTTDGYGCDTRDLLAVELPRPHGHPLALLLPHRHDDGRLRVRSALRAVHAEVGPVRVDDQAVRLRAELWGATLGRGAVVEAVHRRDKERVLTFEARDAGDGAFEAVVDCAALAREHGEEDGKEAIWDFWIRPEEGAPRAALAKLATDVLKPIDVFTFPRPVLTSGAVARPSVVRRAARRARRSLGATPAALPRPVRTELRPYYTALSQFAVKTVRL
>NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MAPRLSVIVPIYDVERYLPACLDSLAAQTFRDFEVLMVDDGSPDDSASIAAAYAERDPRFKLIRKENGGLGAARNTGIAHMSPQAEYVTFVDSDDLIPPDAYRLMVSSLDESGSDFATGNVFHLKGEKTWQVPLLRMLAGEARRATHISRYGKLVADRIACNKVFRRTFWEKHGFAFPEGRLYEDTPVTMRAHYLADAVDVISEPCYYWRLREGESAPSITQRRTDPAGVRDRVTSVLEISAFLAEQPGEMFARLKEEYDTRVLKDDLRLFLNVVPDGDEEYRAEFLRSANRFLDRIDPKVVMALPAQLRVQWLLVRKHKLDELITLLAGQRRKEAVEVSGLVRKYASFPSLADADLDFPRKALRIDQDLRMRAPLQEVTWSEGKLVLSGNAWIDKIDLASKHSSVKVLQLRKDKSRRRILLPARNIHRPECTTNSGQDRYNYDWAGWEVTIDPARLRKGGEWQEGLWHVGLGLYASGLVRRAAVQSSGGAACNFPPYHWLSPDFRLLPSVERGALKIRIERVRALITGRTVEGDRIVVTGEIRVPLAAGENVVLRVRNQKGADVHEYPVTVTDEGGTHRFSVEVPVADVALVFHDGVDAKAQPENRTWSTALIARDPQGAERQFSTVLQEGLPDARFNLPASLGERAELCELAIVAGHTGYLKFAGRTRRATIDRVGVEDGRITIAAHTDPRLTGARFLLKPRNRFEERFVEARWSEDGRFEVAFDPSTLGGGGNVPLRAGRWNLWLRPEDGAPDVPFVTDRLAADQFPLRAELNGRRYWLENRWADFPQLNCRSELSDLERGPFRQKQLRRDLYQPLRRQPLRDQVFYLSYNGKQFSDSPKAMYQELVRRGSDLKHLWAVRDGQVILPEGVEPVRMWGTEWYEALATSRYIVTNGHLPDWIERRPGQVIVQTWHGTMLKKIGHDIDTLHFDRRYQEKLALEAKQWSLVVSSNRFSTPILKRAFSYDGEILEAGYPRNDYLYSPDKDRIAERVKKQLGLPEGKKVVLYAPTWRDDLSHSAGQYLFDLRIDLEDAQRRLGDDHVLLIRRHSNVVDAVPGAGNGFVWDVSEYPDIADLYLAADVMITDYSSVMFDYAHLRRPMLFFTYDLEHYRDTLRGFYFDFEQDSPGPLIATSKELVDALRDIDQVSAEYQERFERFHHLFCDLDDGNASTRVVDRMLEQSREL
>NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MPKLSLVVPVYKVQGYLPECLDSVLGQDYTDFEIIAVDDCSPDGSGAILDEYARRDARIHVIHLTENVGLGRARNAGLEKAQGEYVLFLDSDDTLSDGALTAISERLAATGDPEILVFDYARTYWDGQVRPNQRADLLKSDGPEVFRLAERPQLLDLLQIVWNKAYRRDFITRTGLTFPPGYYEDAPWTFCSLISAERIAVLDRVCVLYRQRREGGNILKTVSRKHFDVFDQYRRVFDFLDAHEELDRWRGPLFRKMVDHYLTVLERPGRLPREARAEFFHRASADYRARLPKGFQKPAGGRGHKYAMLERDAYAAMMSASTAVKLRRTVRKRTRDALNRSKRSAMGVHYQSQLRLPLDENLVLFSAYWSRSVSCNPAAIDAELARLAPHLRRVWAIRPDAVDQVPKGVEYVRVGSRAYWTALARAKYLVNNVNFADAVVKREGQIHLQTHHGTPLKTMGLDQQKYPASTDMNFEKLLERCDRWDYSISSNRFSTAIWERVYPCSYVSLETGYPRNDVLVNAGAEEVRRARAALGLADGAKAFLYMPTHREYQPGFTPSLDLARLAEELGPDVTLLLRGHYFYGSSPHIAELRRSGRIVDVSGHPRVEELYLAADALITDYSSAMFDYAVLDRPIIVYAPDWDIYSAVRGTYFDLLQEPPGAVATSQAELIRLLGSGDYDSRDAAGRRDAFRRRFCEFDDGHAAERVVRRVFLGDQTPLPFVPFDERSHAPTPAQALEPVERA
>NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE
MSWLVTGGAGYIGAHVVRAMAAGGERVVVYDDLSTGSADRVPDGVPLVVGSVLDASLLARAIRDHAVTGVVHIAAKKQVGESVEQPLRYYRENVTGLRTLLEVMTDAGVGKLVFSSSAAVYGMPDVELVTEDTPCAPMSPYGETKLVGEWLIAATARAHGIRAASLRYFNVAGAAEPALADAGVFNLIPMVFERLEAGEAPRIFGDDYATPDGTCVRDYIHVEDIASAHLAAARRLGEAAEGTNLVLNIGRGEGSSVREMVDRILKITGHEHLTPAVAERRPGDPARVVASADRIRRELDWSAHHDLDDMIRSAWQGWRHLRG
>NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase
MGEARRIVVKVGSSSLTTAEGGLDADRVDALVDVLAKVRSGGEREIVLVSSGAIAAGLAPLGLRRRPRDLARQQAAASVGQGLLVARYTASFARYGVRVGQVLLTSDDMSRRAHHRNASRTLDKLLAMGAFPIVNENDTVATDEIRFGDNDRLAALVAHLVHADLLVLLSDVDGVYDGDPGRPGTARIAEVRRPEDLAHVEIGSAGKAGVGTGGMVTKVEAARIAAAAGIPVVLTSAVHAADALTGQDTGTYFHPTGKRSADRLLWLQHASTPQGALTLDDGAVRAVVEGRKSLLPAGIAAVEGEFVAGDPVELRDGEGRAVARGLVSFDAKEIPRLIGRSTRELARELGPAYEREVVHRDDLVILHP

Crispr_ID: NZ_LN831790_13

• CRISPR_ID: NZ_LN831790_13
• CRISPR_location: 5460373-5460452
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_13

Consensus_repeat	Method
CCGCCACCGAGCCGGCCGCCGAG	CRISPRCasFinder

spacers of NZ_LN831790_13

>13.1|5460396|34|NZ_LN831790|CRISPRCasFinder
AAGACGACCGCCAAGAAGGCGGCGGCCAAGAAGA

CRISPR arrays and Neighbor proteins around NZ_LN831790_13

CRISPR arrays

The CRISPR arrays of NZ_LN831790_13

>merge|NZ_LN831790|13|5460373-5460452|CRISPRCasFinder
CGGCCAAGAAGACGGCCGCGAAGAAGACGACCGCCAAGAAGGCGGCGGCCAAGAAGACCGCCACCAAGACGGCGGCCAGG

>NZ_LN831790|13|13|5460373-5460452|CRISPRCasFinder
CGGCCAAGAAGACGGCCGCGAAG	AAGACGACCGCCAAGAAGGCGGCGGCCAAGAAGA
CCGCCACCAAGACGGCGGCCAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	unknown	unknown	gnl|CDD|133014
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	unknown	unknown	gnl|CDD|274574
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	unknown	unknown	gnl|CDD|340847
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	unknown	unknown	gnl|CDD|379420
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	unknown	unknown	gnl|CDD|235460
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	unknown	unknown	gnl|CDD|237560
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2	unknown	unknown	gnl|CDD|274573
NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl|CDD|224012
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	unknown	unknown	gnl|CDD|235510
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	unknown	unknown	gnl|CDD|188475
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	unknown	unknown	gnl|CDD|179085
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	unknown	unknown	gnl|CDD|223362
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	unknown	unknown	gnl|CDD|237562
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	unknown	unknown	gnl|CDD|378393
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	unknown	unknown	gnl|CDD|237045
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	unknown	unknown	gnl|CDD|235464
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|341453

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein	gnl|CDD|133014	cd02523, PC_cytidylyltransferase, Phosphocholine cytidylyltransferases catalyze the synthesis of CDP-choline. This family contains proteins similar to prokaryotic phosphocholine (P-cho) cytidylyltransferases. Phosphocholine (PC) cytidylyltransferases catalyze the transfer of a cytidine monophosphate from CTP to phosphocholine to form CDP-choline. PC is the most abundant phospholipid in eukaryotic membranes and it is also important in prokaryotic membranes. For pathogenic prokaryotes, the cell surface PC facilitates the interaction with host surface and induces attachment and invasion. In addition cell wall PC serves as scaffold for a group of choline-binding proteins that are secreted from the cells. Phosphocholine (PC) cytidylyltransferase is a key enzyme in the prokaryotic choline metabolism pathway. It has been hypothesized to consist of a choline transport system, a choline kinase, CTP:phosphocholine cytidylyltransferase, and a choline phosphotransferase that transfers P-Cho from CDP-Cho to either lipoteichoic acid or lipopolysaccharide.	1.88115e-61
NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD	gnl|CDD|274574	TIGR03426, shape_MreD, rod shape-determining protein MreD. Members of this protein family are the MreD protein of bacterial cell shape determination. Most rod-shaped bacteria depend on MreB and RodA to achieve either a rod shape or some other non-spherical morphology such as coil or stalk formation. MreD is encoded in an operon with MreB, and often with RodA and PBP-2 as well. It is highly hydrophobic (therefore somewhat low-complexity) and highly divergent, and therefore sometimes tricky to discover by homology, but this model finds most examples. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	7.73759e-15
NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase	gnl|CDD|340847	cd03820, GT4_AmsD-like, amylovoran biosynthesis glycosyltransferase AmsD and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. AmSD in Erwinia amylovora has been shown to be involved in the biosynthesis of amylovoran, the acidic exopolysaccharide acting as a virulence factor. This enzyme may be responsible for the formation of galactose alpha-1,6 linkages in amylovoran.	1.01466e-84
NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein	gnl|CDD|379420	pfam14017, DUF4233, Protein of unknown function (DUF4233). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 122 and 147 amino acids in length. Proteins in this family are integral membrane proteins.	9.09264e-23
NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase	gnl|CDD|235460	PRK05429, PRK05429, gamma-glutamyl kinase; Provisional.	0
NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC	gnl|CDD|237560	PRK13922, PRK13922, rod shape-determining protein MreC; Provisional.	5.32001e-68
NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|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_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.96151e-110
NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE	gnl|CDD|224012	COG1087, GalE, UDP-glucose 4-epimerase [Cell envelope biogenesis, outer membrane].	7.07431e-136
NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21	gnl|CDD|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	1.58441e-39
NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein	gnl|CDD|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	0
NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase	gnl|CDD|179085	PRK00668, ndk, mulitfunctional nucleoside diphosphate kinase/apyrimidinic endonuclease/3'-; Validated.	2.06794e-76
NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	6.06473e-155
NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	gnl|CDD|223362	COG0285, FolC, Folylpolyglutamate synthase [Coenzyme metabolism].	6.7133e-138
NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein	gnl|CDD|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0
NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein	gnl|CDD|378393	pfam10105, DUF2344, Uncharacterized protein conserved in bacteria (DUF2344). This domain, found in various hypothetical bacterial proteins and Radical Sam domain proteins, has no known function. This domain is distantly related to tRNA pseudouridine synthases, suggesting this family may carry out a function related to RNA modification. But this family appears to lack the catalytic aspartate found in pseudouridine synthases.	1.62633e-69
NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE	gnl|CDD|237045	PRK12296, obgE, GTPase CgtA; Reviewed.	0
NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|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].	3.40526e-128
NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27	gnl|CDD|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	3.49902e-46
NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein	gnl|CDD|341453	cd08174, G1PDH-like, Glycerol-1-phosphate dehydrogenase-like. These glycerol-1-phosphate dehydrogenase-like proteins have not been characterized. The protein sequences have high similarity with that of glycerol-1-phosphate dehydrogenase (G1PDH) which plays a role in the synthesis of phosphoglycerolipids in Gram-positive bacterial species. It catalyzes the reversibly reduction of dihydroxyacetone phosphate (DHAP) to glycerol-1-phosphate (G1P) in a NADH-dependent manner. Its activity requires Ni++ ion.	1.50094e-144

Protein sequences

>NZ_LN831790.1|WP_029386336.1|5454964_5455741_+|DUF2344-domain-containing-protein
MQRIRLRYTKRGRLRFTSHRDFQRAFERALRRAEVPMAYSAGFTPHPKVSYANAAPTGTGSEAEYLEIALTEPRDPEQLRALLDESLPAGLDVVEAVEARTSGLADRLTASVWELRLDGVEPAEAARAVEAFNAAGAVEVQRLTKNGVRTFDARPAVASLESVETHGSPADRPSDRPCAILRLVVRHVTPAVRPDDVLSGLRAVADLAPPVPAAVTRLAQGLFDEETGTVTDPLAPDREAAANEPQTADATAAAKAPA
>NZ_LN831790.1|WP_029386335.1|5451671_5453624_+|TIGR03960-family-B12-binding-radical-SAM-protein
MPAEAAESVFPQLEALLPHVQKPIQYVGGELNSTVKDWDSCDVRWALMYPDAYEVGLPNQGVMILYEVLNEQEGVLAERTYSVWPDLEALMREHGVPQFTVDSHRPVRAFDVFGLSFSTELGYTNMLAALELAGIPLEARDRGLDDPIVMAGGHAAFNPEPIADFIDCAIIGDGEQAVLEVTALIRAWKAEGRPGGREELLLRLAKTGGVYVPGFYDVEYLPDGRIARVVPNRSGVPWRVSKHTVMDLDEWPYPKQPLVPLAETVHERMSVEIFRGCTRGCRFCQAGMITRPVRERSITGIGEMVEKGLNATGFEEVGLLSLSSADHSEIGDIAKGLADRYADDKIGLSLPSTRVDAFNIDLANELTRNGRRSGLTFAPEGGSERIRKVINKMVSEEDLIRTVATAYGNGWRQVKLYFMCGLPTETDEDVLQIADMATRVIQKGREVSGSNDIRCTVSIGGFVPKPHTPFQWAPQLSAEETDARLAKLRDKIRGDKKYGRSIGFRYHDGKPGIVEGLLSRGDRRIGAVIRAVYEDGGRFDGWREHFSYDRWMSCAEKALAPFGVDVDWYTTRERGYEEVLPWDHLDSGLDKDWLWEDWQDALDETEVEDCRWTPCFDCGVCPQMDTHIQIGPTGKKLLPLTVKNAAPSAG
>NZ_LN831790.1|WP_029383283.1|5450267_5451467_+|rod-shape-determining-protein-RodA
MTGANGFQVSGYGPERAGWTRVFARDSVARRLDWPILLSATALSLIGAVLVYSATRNRTELNQGDPYFFLVRHLLNTGIGIALMIATVWLGHRTLRTAVPLLYGASVFLILLVLTPLGSTVNGAHSWIQLGGGFSVQPSEFVKVTIILGMAMLLAARVDAGDKPYPDHRTVIQALALATVPMLIVMLMPDLGSVMVMVVIVLGVLLASGASNRWVFGLLGAGAVGAVAVWQLGILDEYQINRFAAFANPELDPAGVGYNTNQARIAIGSGGLTGSGLFHGSQTTGQFVPEQQTDFVFTVAGEELGFLGAGFIILLLGVVLWRACRIARETSDLYGTIVAAGIVAWFAFQAFENIGMTLGIMPVTGLPLPFVSYGGSSMFAVWIAVGLLQSITVQRPMSA
>NZ_LN831790.1|WP_029383284.1|5447964_5450271_+|penicillin-binding-protein-2
MTNIPETGRSPRVQIRLVVIQVLVLSLLGTLGGRLWYLQIREGDEYAEKASGNHVQQVVQPAVRGSILDARGVPLADNETRLVVSASRTDLMKMEDDGKAVLTKLAGVLGMRPQEVMEKVRLCDAETPQPCWNGSPYQPIPITDEATPKQALQIRERAEDFPGITAEPQAVRRYPSPGEANTAQVLGYLSPVTDEEIKQAQDSESPYLRSDQVGRSGLERQYDKQLRGKAGVTRYEVDNLGRVIGKAESDAAQPGSNLVTSIDARVQRIAEYELNEAMKAARKEYDRNTGTTYKADSGAVVVMEARTGRVVAMASNPTYDPNAWVGGISSADYQKLTGKNSNYPLLNRAIQGQAAPGSIFKVVSTAAAVEAGYDFDGSYQCSSAYSVGGQVFKNFESANYGAIDLGRALEVSCDTVYYRLAHQEWKKDGGINPKGRPKDHFFKAAHQFGLGKETGIDLPNEVSGRVPDREWKQRYWEANKDAWCKTGKKDGSYVEKIAYENCVEGNKMRAGDEINYSIGQGDTLVTPIQMATIYAAISNGGTLYTPSIGKAIVSPDGKKVSEIEPEPHGRLPISDATRDKMDAALAGVATRGTAAWRFGGWPQDEIPMHAKTGTAEVYGKQTTSWFATYTDDYAIVMTISQGGTGSGASGPAVRKIYDALYGVQEDGSIDRKKALLPEPAKSLPEIKPDGTITAPKTAEDPVKRDRATEQDENAPADTGQPQDDAATVATPAAENRQTRRRRRGGGRGGTTGTGTAARAGTRSRRRCA
>NZ_LN831790.1|WP_029383285.1|5447201_5447873_+|rod-shape-determining-protein-MreD
MRVNRILLSVSLVVVALVIQVSVLARLHLPGAVPDLLLLTVLGLALVYGHVGGALVGFGAGLLADLAPPADHAAGRYALVLCVVGYLAGLVKPENGRLKSAAGPMAVVVAAAVASTLLYAGVGALVGDTAARHVGLPGLLFTAALYDLLLAPFVVPGIMALARRAENDPLAETSSTAQTTDISSGWVAGGTGLRIGGQRNGLRVKAARARVARAGRIKGVKRL
>NZ_LN831790.1|WP_029383286.1|5446232_5447189_+|rod-shape-determining-protein-MreC
MRDTKESRLLLVLLIAIAFALITVDIRGGEDSPVDGARHAAATVFGPIENGVSAAVDPVGNAVAAIRDSGRRHDRLAELEKENAALKAKLGSDDRGRSRLKQLDSMLKIAGKGQYGIKGAQVIAIGAAQGFSWTITIDVGANDGIKRDMTVLNGDGLVGRVTTVGPETATVLLASDPDFTVGTRLEGSDELGFASGQGDRPLRVELLNGKAEVKKGDRLVTFGSQADKPFVPGVPVGVVSRVDPSGGGLTRTLYVTPYVGFTKLDIVGVVVQAPRKDPRDTVLPAEPRPVPTPTVTVTVTPSAEAPADGQYPSEQPEQ
>NZ_LN831790.1|WP_028422119.1|5445000_5446020_+|rod-shape-determining-protein
MSFIGRDMAVDLGTANTLVYVRGRGIVLNEPSVVAINTNTGGILAVGAEAKKMIGRTPGNIVAVRPLKDGVIADFEITERMLRYFILKIHKRRYLARPRVVVCVPSGITGVERRAVIEASSQAGARQVHIIEEPMAAAIGSGLPVHEATGNMVVDIGGGTTEVAVISLGGIVTAQSIRVAGDELDNAIIQHVKKEYSLLLGERTAEQIKITIGSAYDLDTDEHTEIRGRDLVSGLPKTVVISAAEVRKAIEEPVNAIVDAVKTTLDKCPPELSGDIMDRGIVLTGGGALLRGLDERLRRETGMPIHIAEDPLDSVALGSGKCVEEFEALQQVLDAQPRR
>NZ_LN831790.1|WP_029383287.1|5444284_5444698_+|nucleoside-diphosphate-kinase
MTQRTLVLLKPDAVRRGLTGEIISRIERKAGWQITALELRTLDAETLEQHYGEHKGKPFYEPLVEFMASGPVVAMIVEGERVIEGVRQLAGPTDPIAAPAGSIRGDYGVIVRENLIHASDSEESAERELKIFFPGRV
>NZ_LN831790.1|WP_029383288.1|5443836_5444193_+|DUF4233-domain-containing-protein
MRTLCSSTLIGEFFVIAFAGLVAMKDPDLSMAAVWTVSGIAMFLCLVLCGLVTRPGGIALGWALQIALVAAGFVVPTMFFMGAVFAALWWASVHYGRKIDEAKARFAAQAGTQAPDAV
>NZ_LN831790.1|WP_029383289.1|5442309_5443830_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase
MSELPPHDSSEQPDPAGSFDEIIEAETERDPDLAVIEAGSRTLRTQGGPPQADVPARPEDPEVDKALREVEAELATRWGETKLEPSVSRIAALMDVLGEPQRSYPSIHITGTNGKTSTARMIEALLGAFDLRTGRYTSPHVQSITERISLDGAPISAERFIETYQDVKPYVEMVDGRQEYRLSFFEVLTGMAYAAFADAPVDVAVVEVGMGGSWDATNVIDGDVAVVTPIDLDHTDRLGSTTAEIATEKAGIIKQDATVILAQQPVDAAQALLKKAVDVGATVAREGLEFGVVARQVAVGGQLLTLRGLGGEYTEVYLPLHGAHQAHNAAVALAAVEAFFGVGAQRAETLDIDTVRKAFAAVSSPGRLEVVRRSPTVVLDAAHNPAGARVTADAIGEAFQFSRLIGVVGASADKDVRGLLEAFEPVFAEVVVTQNSSHRAMDADALAAVAVEVFGEERVQVEPRLPDALEAAITLAEEEGEFAGGGVLVTGSVITVGEARLLLGRG
>NZ_LN831790.1|WP_047122034.1|5460653_5461406_+|phosphocholine-cytidylyltransferase-family-protein
MIGLILAAGAGRRLRPYTDTLPKALVPVGPEGAEDSLTVLDLTLGNFAEVGLTEAAIIVGYRKEAVYARKEALEAKYGLKLTLIDNDKAEEWNNAYSLWCGREALKDGVILANGDTVHPVSVEKTLLAARGDGKKIILALDTVKQLAEEEMKVVVDPAKGVRRITKLMDPAEATGEYIGVTLIEGEAAAELADALKATFERDPQLYYEDGYQELVDRGFTVDVAPIGDVRWVEIDNHDDLAKGREIACRY
>NZ_LN831790.1|WP_029387502.1|5461393_5462455_+|iron-containing-alcohol-dehydrogenase-family-protein
MPLLTRLIPAPVVVDIRAGALDDLTSVLADQRISQSGRLAVAVSGGSGARLRERLAPALPGAEWFEVGGGTIDDAVRLADAMKGGRYDAVVGLGGGKVIDCAKYSAARVGLPMVAVATNLSHDGICSPVSILDNDAGRGSYGVPTPIAILVDLAVIREAPIRFVRSGIGDAVSNISAVADWELAHRVNGEKVDGLAAAMARQAGEAVLRHPGGCGDDGFLTVLTEGLVLSGIAMSIAGHTRPSSGACHEISHALDLLYPRRAASHGEQVGLGAAFAMHLRGDHEGSRLMAGVLRRHGLPVLAEEIGFDDDEFVRAVEFAPQTRPGRYTILEHLELSPARIREAYADYAASVDD
>NZ_LN831790.1|WP_004001309.1|5462645_5462966_+|50S-ribosomal-protein-L21
MYAIVRSGGRQHKVAVGDIVEVDKISTAKVGDTVELSTLLVVDGDSVTSDPWVLAGIKVQAEVVDHHKGQKIDILRYKNKTGYRRRQGHRQQYTAIKVTEIPTAAK
>NZ_LN831790.1|WP_029387501.1|5462980_5463235_+|50S-ribosomal-protein-L27
MAHKKGASSTRNGRDSNAQRLGVKRFGGQVVNAGEILVRQRGTHFHPGSGVGRGGDDTLFALQAGSVQFGTHRGRKVVNIVPVA
>NZ_LN831790.1|WP_029387500.1|5463431_5464868_+|GTPase-ObgE
MTTFVDRVELHVAAGNGGHGCASVHREKFKPLGGPDGGNGGRGGDVILTVDQSVTTLLEYHHSPHRKATNGKPGEGGHRSGKDGQDLVLAVPDGTVVLDKAGNVLADLVGHGTSYVAAQGGRGGLGNAALASARRKAPGFALLGEPGDVCEIVLELKTVADVALVGYPSAGKSSLISVLSAAKPKIADYPFTTLVPNLGVVTAGSTVYTIADVPGLIPGASQGKGLGLEFLRHVERCSVLVHVLDTATLESDRDPVSDLDVIEEELRQYGGLDNRPRLVVLNKIDVPDGRDLAEMVRPDLQARGYRVFEVSAVAHTGLKELSFALAELVAAARAARPKEEATRIVIRPKAVDDAGFTVTREEDGLFRVRGEKPERWVRQTDFNNDEAVGYLADRLNRLGVEEELMKAGARAGDGVAIGPEENAVVFDWEPSVMAGAEMLGRRGEDHRLEAPRPAAQRRRDRQAERDDAQREFDDFEPF
>NZ_LN831790.1|WP_048573623.1|5465283_5467281_+|glycosyltransferase
MGGVVSATQNLAGALADRHEVEIVALRKVRDESYFPLDPRVSVRVLSDLRPHSPVSDLDDPLVEKWPLVYPPNTGAKKPVVSRLAERRLLEYLATTDADVVVSSSPRNTIMLAQAPGTYLKVAQEHSMPSIYAKDIKERLFPAYLSLDALTALTPEEVESIGRQVPAVRDRLAVMPNCVPASPIRSKGTNKVVVCAGHLTDNKNHALLVEAFAKVHAQAPDWTLRIYGSGAEKARLRARIEELGLSNSILLMGQTAPVTPEFGKGSIFVLPSKREAFGNVIVEAMAAGLPVVSTDADHGPRNILTPGEDGLLVPRGDVEEMARAILRLVQDDELRQKMAANAVRGAERFHETASRERFEAILERALARKALPRHATARVDDRGSVHIEVGPLPERARGAELVLRRSGKNGEEHRFPLSDSGEALVAWDAGLPHGTWEAALASPSGGEVPLTTDGYGCDTRDLLAVELPRPHGHPLALLLPHRHDDGRLRVRSALRAVHAEVGPVRVDDQAVRLRAELWGATLGRGAVVEAVHRRDKERVLTFEARDAGDGAFEAVVDCAALAREHGEEDGKEAIWDFWIRPEEGAPRAALAKLATDVLKPIDVFTFPRPVLTSGAVARPSVVRRAARRARRSLGATPAALPRPVRTELRPYYTALSQFAVKTVRL
>NZ_LN831790.1|WP_029387498.1|5467389_5470950_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MAPRLSVIVPIYDVERYLPACLDSLAAQTFRDFEVLMVDDGSPDDSASIAAAYAERDPRFKLIRKENGGLGAARNTGIAHMSPQAEYVTFVDSDDLIPPDAYRLMVSSLDESGSDFATGNVFHLKGEKTWQVPLLRMLAGEARRATHISRYGKLVADRIACNKVFRRTFWEKHGFAFPEGRLYEDTPVTMRAHYLADAVDVISEPCYYWRLREGESAPSITQRRTDPAGVRDRVTSVLEISAFLAEQPGEMFARLKEEYDTRVLKDDLRLFLNVVPDGDEEYRAEFLRSANRFLDRIDPKVVMALPAQLRVQWLLVRKHKLDELITLLAGQRRKEAVEVSGLVRKYASFPSLADADLDFPRKALRIDQDLRMRAPLQEVTWSEGKLVLSGNAWIDKIDLASKHSSVKVLQLRKDKSRRRILLPARNIHRPECTTNSGQDRYNYDWAGWEVTIDPARLRKGGEWQEGLWHVGLGLYASGLVRRAAVQSSGGAACNFPPYHWLSPDFRLLPSVERGALKIRIERVRALITGRTVEGDRIVVTGEIRVPLAAGENVVLRVRNQKGADVHEYPVTVTDEGGTHRFSVEVPVADVALVFHDGVDAKAQPENRTWSTALIARDPQGAERQFSTVLQEGLPDARFNLPASLGERAELCELAIVAGHTGYLKFAGRTRRATIDRVGVEDGRITIAAHTDPRLTGARFLLKPRNRFEERFVEARWSEDGRFEVAFDPSTLGGGGNVPLRAGRWNLWLRPEDGAPDVPFVTDRLAADQFPLRAELNGRRYWLENRWADFPQLNCRSELSDLERGPFRQKQLRRDLYQPLRRQPLRDQVFYLSYNGKQFSDSPKAMYQELVRRGSDLKHLWAVRDGQVILPEGVEPVRMWGTEWYEALATSRYIVTNGHLPDWIERRPGQVIVQTWHGTMLKKIGHDIDTLHFDRRYQEKLALEAKQWSLVVSSNRFSTPILKRAFSYDGEILEAGYPRNDYLYSPDKDRIAERVKKQLGLPEGKKVVLYAPTWRDDLSHSAGQYLFDLRIDLEDAQRRLGDDHVLLIRRHSNVVDAVPGAGNGFVWDVSEYPDIADLYLAADVMITDYSSVMFDYAHLRRPMLFFTYDLEHYRDTLRGFYFDFEQDSPGPLIATSKELVDALRDIDQVSAEYQERFERFHHLFCDLDDGNASTRVVDRMLEQSREL
>NZ_LN831790.1|WP_029387497.1|5470973_5473205_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MPKLSLVVPVYKVQGYLPECLDSVLGQDYTDFEIIAVDDCSPDGSGAILDEYARRDARIHVIHLTENVGLGRARNAGLEKAQGEYVLFLDSDDTLSDGALTAISERLAATGDPEILVFDYARTYWDGQVRPNQRADLLKSDGPEVFRLAERPQLLDLLQIVWNKAYRRDFITRTGLTFPPGYYEDAPWTFCSLISAERIAVLDRVCVLYRQRREGGNILKTVSRKHFDVFDQYRRVFDFLDAHEELDRWRGPLFRKMVDHYLTVLERPGRLPREARAEFFHRASADYRARLPKGFQKPAGGRGHKYAMLERDAYAAMMSASTAVKLRRTVRKRTRDALNRSKRSAMGVHYQSQLRLPLDENLVLFSAYWSRSVSCNPAAIDAELARLAPHLRRVWAIRPDAVDQVPKGVEYVRVGSRAYWTALARAKYLVNNVNFADAVVKREGQIHLQTHHGTPLKTMGLDQQKYPASTDMNFEKLLERCDRWDYSISSNRFSTAIWERVYPCSYVSLETGYPRNDVLVNAGAEEVRRARAALGLADGAKAFLYMPTHREYQPGFTPSLDLARLAEELGPDVTLLLRGHYFYGSSPHIAELRRSGRIVDVSGHPRVEELYLAADALITDYSSAMFDYAVLDRPIIVYAPDWDIYSAVRGTYFDLLQEPPGAVATSQAELIRLLGSGDYDSRDAAGRRDAFRRRFCEFDDGHAAERVVRRVFLGDQTPLPFVPFDERSHAPTPAQALEPVERA
>NZ_LN831790.1|WP_029387496.1|5473548_5474520_+|UDP-glucose-4-epimerase-GalE
MSWLVTGGAGYIGAHVVRAMAAGGERVVVYDDLSTGSADRVPDGVPLVVGSVLDASLLARAIRDHAVTGVVHIAAKKQVGESVEQPLRYYRENVTGLRTLLEVMTDAGVGKLVFSSSAAVYGMPDVELVTEDTPCAPMSPYGETKLVGEWLIAATARAHGIRAASLRYFNVAGAAEPALADAGVFNLIPMVFERLEAGEAPRIFGDDYATPDGTCVRDYIHVEDIASAHLAAARRLGEAAEGTNLVLNIGRGEGSSVREMVDRILKITGHEHLTPAVAERRPGDPARVVASADRIRRELDWSAHHDLDDMIRSAWQGWRHLRG
>NZ_LN831790.1|WP_029387495.1|5474683_5475790_+|glutamate-5-kinase
MGEARRIVVKVGSSSLTTAEGGLDADRVDALVDVLAKVRSGGEREIVLVSSGAIAAGLAPLGLRRRPRDLARQQAAASVGQGLLVARYTASFARYGVRVGQVLLTSDDMSRRAHHRNASRTLDKLLAMGAFPIVNENDTVATDEIRFGDNDRLAALVAHLVHADLLVLLSDVDGVYDGDPGRPGTARIAEVRRPEDLAHVEIGSAGKAGVGTGGMVTKVEAARIAAAAGIPVVLTSAVHAADALTGQDTGTYFHPTGKRSADRLLWLQHASTPQGALTLDDGAVRAVVEGRKSLLPAGIAAVEGEFVAGDPVELRDGEGRAVARGLVSFDAKEIPRLIGRSTRELARELGPAYEREVVHRDDLVILHP

Crispr_ID: NZ_LN831790_14

• CRISPR_ID: NZ_LN831790_14
• CRISPR_location: 5600114-5600208
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831790_14

Consensus_repeat	Method
CGGTCGCCCTCCGCCTGGGACGG	CRISPRCasFinder

spacers of NZ_LN831790_14

>14.1|5600137|49|NZ_LN831790|CRISPRCasFinder
CGTCGGGTGCGGCGGGGACTGGCGGCCGGGCGTGTCGCGCTCGTCGTCG

CRISPR arrays and Neighbor proteins around NZ_LN831790_14

CRISPR arrays

The CRISPR arrays of NZ_LN831790_14

>merge|NZ_LN831790|14|5600114-5600208|CRISPRCasFinder
CGGTCGCCCTCCGCCTGGGACGGCGTCGGGTGCGGCGGGGACTGGCGGCCGGGCGTGTCGCGCTCGTCGTCGCGGTCGCCCTCGGCCTGGGACGG

>NZ_LN831790|14|14|5600114-5600208|CRISPRCasFinder
CGGTCGCCCTCCGCCTGGGACGG	CGTCGGGTGCGGCGGGGACTGGCGGCCGGGCGTGTCGCGCTCGTCGTCG
CGGTCGCCCTCGGCCTGGGACGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_078648339.1|5604814_5605846_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|379605
NZ_LN831790.1|WP_029385726.1|5598530_5598794_-|type-II-toxin-antitoxin-system-prevent-host-death-family-antitoxin	unknown	unknown	gnl|CDD|171099
NZ_LN831790.1|WP_029385722.1|5593577_5595032_-|sugar-kinase	unknown	unknown	gnl|CDD|198375
NZ_LN831790.1|WP_029385732.1|5603506_5604223_-|ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|198080
NZ_LN831790.1|WP_029385718.1|5586127_5588032_+|DNA-primase	unknown	unknown	gnl|CDD|235551
NZ_LN831790.1|WP_063833346.1|5600219_5601092_-|cytochrome-c-oxidase-assembly-protein	unknown	unknown	gnl|CDD|378238
NZ_LN831790.1|WP_176572968.1|5588453_5589620_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|235640
NZ_LN831790.1|WP_029385731.1|5602185_5603388_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029385723.1|5595134_5595437_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_029385730.1|5601614_5602184_-|hemerythrin-domain-containing-protein	unknown	unknown	gnl|CDD|213983
NZ_LN831790.1|WP_029385736.1|5607372_5608410_-|rod-shape-determining-protein	unknown	unknown	gnl|CDD|336482
NZ_LN831790.1|WP_029385720.1|5589786_5591715_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_LN831790.1|WP_029385721.1|5591714_5593448_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_LN831790.1|WP_049976854.1|5596813_5598286_+|NACHT-domain-containing-protein	unknown	unknown	gnl|CDD|227922
NZ_LN831790.1|WP_029385737.1|5608732_5612350_+|S8-family-serine-peptidase	unknown	unknown	gnl|CDD|173815
NZ_LN831790.1|WP_029385735.1|5605864_5607352_-|GAF-domain-containing-protein	unknown	unknown	gnl|CDD|214500
NZ_LN831790.1|WP_047122048.1|5599017_5599896_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_LN831790.1|WP_047122050.1|5604449_5604818_+|STAS-domain-containing-protein	unknown	unknown	gnl|CDD|132914
NZ_LN831790.1|WP_047122049.1|5601147_5601618_-|DUF2243-domain-containing-protein	unknown	unknown	gnl|CDD|370775
NZ_LN831790.1|WP_029385725.1|5598279_5598534_-|Txe/YoeB-family-addiction-module-toxin	unknown	unknown	gnl|CDD|284238

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_078648339.1|5604814_5605846_+|sensor-histidine-kinase	gnl|CDD|379605	pfam14417, MEDS, MEDS: MEthanogen/methylotroph, DcmR Sensory domain. MEDS is prototyped by DcmR and is likely to function with the PocR domain in certain organisms in sensing hydrocarbon derivatives. The MEDS domain occurs fused to Histidine Kinase and as stand-alone version. Sequence analysis shows that it is a catalytically inactive version of the P-loop NTPase domain of the RecA superfamily.	8.21639e-43
NZ_LN831790.1|WP_029385726.1|5598530_5598794_-|type-II-toxin-antitoxin-system-prevent-host-death-family-antitoxin	gnl|CDD|171099	PRK11409, PRK11409, YoeB-YefM toxin-antitoxin system antitoxin YefM.	3.54156e-22
NZ_LN831790.1|WP_029385722.1|5593577_5595032_-|sugar-kinase	gnl|CDD|198375	cd07809, FGGY_D-XK_1, D-xylulose kinases, subgroup 1; members of the FGGY family of carbohydrate kinases. This subgroup is composed of D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17) from bacteria and eukaryota. They share high sequence similarity with Escherichia coli xylulokinase (EcXK), which catalyzes the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. Some uncharacterized sequences are also included in this subfamily. EcXK exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of Mg2+ or Mn2+ might be required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	7.43325e-116
NZ_LN831790.1|WP_029385732.1|5603506_5604223_-|ANTAR-domain-containing-protein	gnl|CDD|198080	smart01012, ANTAR, ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	7.4007e-15
NZ_LN831790.1|WP_029385718.1|5586127_5588032_+|DNA-primase	gnl|CDD|235551	PRK05667, dnaG, DNA primase; Validated.	0
NZ_LN831790.1|WP_063833346.1|5600219_5601092_-|cytochrome-c-oxidase-assembly-protein	gnl|CDD|378238	pfam09678, Caa3_CtaG, Cytochrome c oxidase caa3 assembly factor (Caa3_CtaG). Members of this family are the CtaG protein required for assembly of active cytochrome c oxidase of the caa3 type, as found in Bacillus subtilis.	1.33938e-40
NZ_LN831790.1|WP_176572968.1|5588453_5589620_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|235640	PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.	1.07492e-163
NZ_LN831790.1|WP_029385736.1|5607372_5608410_-|rod-shape-determining-protein	gnl|CDD|336482	pfam06723, MreB_Mbl, MreB/Mbl protein. This family consists of bacterial MreB and Mbl proteins as well as two related archaeal sequences. MreB is known to be a rod shape-determining protein in bacteria and goes to make up the bacterial cytoskeleton. Genes coding for MreB/Mbl are only found in elongated bacteria, not in coccoid forms. It has been speculated that constituents of the eukaryotic cytoskeleton (tubulin, actin) may have evolved from prokaryotic precursor proteins closely related to today's bacterial proteins FtsZ and MreB/Mbl.	4.04595e-139
NZ_LN831790.1|WP_029385730.1|5601614_5602184_-|hemerythrin-domain-containing-protein	gnl|CDD|213983	cd12108, Hr-like, Hemerythrin-like domain. Hemerythrin (Hr) like domains have the same four alpha helix bundle and a similar, but slightly different active site structure than hemerythrin. They are non-heme diiron binding proteins mainly found in bacteria and eukaryotes. Like Hr, they may be involved in oxygen transport or like human FBXL5 (F-box and leucine-rich repeat protein 5), a member of this group, play a role in cellular iron homeostasis.	2.34188e-10
NZ_LN831790.1|WP_029385720.1|5589786_5591715_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_LN831790.1|WP_029385721.1|5591714_5593448_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	2.08794e-159
NZ_LN831790.1|WP_049976854.1|5596813_5598286_+|NACHT-domain-containing-protein	gnl|CDD|227922	COG5635, COG5635, Predicted NTPase (NACHT family) [Signal transduction mechanisms].	1.38451e-11
NZ_LN831790.1|WP_029385737.1|5608732_5612350_+|S8-family-serine-peptidase	gnl|CDD|173815	cd07490, Peptidases_S8_6, Peptidase S8 family domain, uncharacterized subfamily 6. This family is a member of the Peptidases S8 or Subtilases serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	3.58744e-82
NZ_LN831790.1|WP_029385735.1|5605864_5607352_-|GAF-domain-containing-protein	gnl|CDD|214500	smart00065, GAF, Domain present in phytochromes and cGMP-specific phosphodiesterases. Mutations within these domains in PDE6B result in autosomal recessive inheritance of retinitis pigmentosa.	1.37328e-10
NZ_LN831790.1|WP_047122048.1|5599017_5599896_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.1104e-14
NZ_LN831790.1|WP_047122050.1|5604449_5604818_+|STAS-domain-containing-protein	gnl|CDD|132914	cd07043, STAS_anti-anti-sigma_factors, Sulphate Transporter and Anti-Sigma factor antagonist) domain of anti-anti-sigma factors, key regulators of anti-sigma factors by phosphorylation. Anti-anti-sigma factors play an important role in the regulation of several sigma factors and their corresponding anti-sigma factors. Upon dephosphorylation they bind the anti-sigma factor and induce the release of the sigma factor from the anti-sigma factor. In a feedback mechanism the anti-anti-sigma factor can be inactivated via phosphorylation by the anti-sigma factor. Well studied examples from Bacillus subtilis are SpoIIAA (regulating sigmaF and sigmaC which play an important role in sporulation) and RsbV (regulating sigmaB involved in the general stress response). The STAS domain is also found in the C- terminal region of sulphate transporters and stressosomes.	1.9487e-12
NZ_LN831790.1|WP_047122049.1|5601147_5601618_-|DUF2243-domain-containing-protein	gnl|CDD|370775	pfam10002, DUF2243, Predicted membrane protein (DUF2243). This domain, found in various hypothetical bacterial proteins, has no known function.	2.15539e-50
NZ_LN831790.1|WP_029385725.1|5598279_5598534_-|Txe/YoeB-family-addiction-module-toxin	gnl|CDD|284238	pfam06769, YoeB_toxin, YoeB-like toxin of bacterial type II toxin-antitoxin system. YoeB_toxin is a family of bacterial toxins that forms one component of the type II toxin-antitoxin system in E. coli whose antitoxin is represented by YefM, found in pfam02604. The plasmid encoded Axe-Txe proteins in Enterococcus faecium act as an antitoxin-toxin pair. When the plasmid is lost, the antitoxin is degraded relatively quickly by host enzymes. This allows the toxin to interact with its intracellular target, thus killing the cell or impeding cell growth. These toxins are highly potent protein synthesis inhibitors, specifically blocking the initiation of translation. In the case of YoeB, it binds to the 50 S ribosomal subunit in 70 S ribosomes and interacts with the A site leading to mRNA cleavage at this site. As a result, the 3'-end portion of the mRNA is released from ribosomes, and translation initiation is effectively inhibited.	2.20872e-47

Protein sequences

>NZ_LN831790.1|WP_047122048.1|5599017_5599896_-|class-I-SAM-dependent-methyltransferase
MSGRLDPATRRRIAENRRNWDARARVHADSPYYSLTERAAETRFHPREWEQLGPLDGRSVLHLQCHNGAETLAFAQKGARTTGLDFSGGNLAVARRSARAAGVSVDFVEADVYDAVTALDGRTFDLVYTGRGSLPYLPDLDEWARVVARLLEPGGLVRLMEYHPLLNSLGRTGPRDPERPLELRHDYLGGGGPLTFDTPHTYAPSRSGLLVEGATVSHEWPHTVVDVLHALHGAGLAVDLDLLWETDWLDWPRWDGMTQVAPGWWRRPEGGISIPLMYTAGARSPAAATATS
>NZ_LN831790.1|WP_029385726.1|5598530_5598794_-|type-II-toxin-antitoxin-system-prevent-host-death-family-antitoxin
MSITASEARQNLFPLIEQVNEDHAPVHITSRKGNAVLMSEEDFNSWTETVHLLRSPKNARRLLDSIAEAEAGEVQHRELIDPDAERA
>NZ_LN831790.1|WP_029385725.1|5598279_5598534_-|Txe/YoeB-family-addiction-module-toxin
MRISFTSHAWGDYTYWAESDRKMVKRINKLIDDTMRDPFKGIGKPEPLKGDLSGYWSRRIDDTHRLVYKPTDDELIIVQARYHY
>NZ_LN831790.1|WP_049976854.1|5596813_5598286_+|NACHT-domain-containing-protein
MRRGNRHTRLALWGLGLAVAIPVVGALLWTARTLGDGKLGAGDQAGVLGFGAAAVGVLLGVASLVVAWLGYRVDRRESATATGTAAIADAFALAVRDEWEAEARLRRLNDPYALPVSWTAADEELVEPWADLIARSDAREASVTGPADLSGRDDGIGDLFQHRLPIRRLVVLGEPGSGKSMLLVRLLLDLCARRSSGDPVPVLFSLSVWDPAADDLIPWLEQQLCTHYPALAAERDGSTRARALLEHRLVLPLLDGFDEMAPAAQAVALDAINRALPVGHPFVLSSRTAEYRRALTPHSGVPVRLNGAAAIVLEPLGSDTAAAYLARDAGGIHSASAARWSPVLARLGTHSPVGEALDTPLTLFLARTIYNPRPGDGADDLPDPARLCNERDFPDADAVRTHLFEAYVPRPRPRPLLRAGKRTCRATPGWRPGRAARSHLEPGRRARGRRSVHAHPRGRPLPFEGCRSRRASRYRTASLQRRVFGPCRCQ
>NZ_LN831790.1|WP_029385723.1|5595134_5595437_-|hypothetical-protein
MRYRLTFVVGLAVGYVLGTRAGRERYEQLKKSARRVSQNPAVRNTAESAAQQGRQFADKAYHVVSDKVGDRMPESVTQRVRSLRERGGNGRADDWGTSDT
>NZ_LN831790.1|WP_029385722.1|5593577_5595032_-|sugar-kinase
MGIVAGLDSSPDFTRIVVCDTDTGAVLRQGYAPHPVESPEGGGRPSDIDPQAWLLSLGEAAAGGLLEGVQAIGVSAQANAVVPLDAQGNTVRPAMIGGDKRAQVAAADLVDALGGREAWAQAVGCVPQAAHPVTKLRWLARTEPEAAARAAVLLQAHDWLVWQLLGRPLRRTTDRGGASGTGYWSAASGAWRPDLVELALGHQAALPEVIGPSDAAGTTPEGLLISAGTGETMAAAFGLGVGLGDAVVSLGASGSVMAVHSEPLVDHSGMITALADATGLHLPVVTTLNAVRALRGTAELLGLPDLESLSELAMKSTPGAHGLVLLPYLEGERTPTLPHTAGTLAGLRRESMKPEHLARAAFEGMLCGLADALDVLRGRGVEVRRIFLLGPAAELPAVQAVAPALFGTQVVVPQPADYAAIGAARQAAWALGVSQGTLDPRTPPAWQGAAAQVLEPGEELAAGQAVRQQYVSVREQTHPGAFRA
>NZ_LN831790.1|WP_029385721.1|5591714_5593448_-|ABC-transporter-ATP-binding-protein
MLIRLLRTCLRPYKNTIALLVALQFLQTCATLYLPTLNADIIDHGVVQGDTGYILVYGALMIGISLVQVVCNIGAVYYGARTASALGRDLRAAVFDRVQSFSAREVGRFGAPSLITRTTNDVQQVQMLALMTFTLMVSAPIMCVGGIVMALGLDVPLSGVLVAVVPVLGICVTLIVRRLRPLFRAMQERLDTVNRVLREQITGNRVIRAFVRDEYEQRRFGKANADLTEVALGSGNLLALMFPVVMTVVNVSSIAVVWFGAHRIDSGRMEIGDLTAFLAYLMQIVMSVMMATFMFMMVPRAEVCAERIQEVLDTSSSVVPPVTPVTRLRQRGHLEIRDAGFRYPGAEEPVLRGVRLVARPGETTAVIGSTGSGKSTLLGLVPRLFDATEGEVLVDGVDVRTVEPALLARTVGLVPQKPYLFAGTVATNLRYGNPDATDEELWHALEVAQAREFVERLEGRLDAPIAQGGTNVSGGQRQRLAIARTLVQRPEIYLFDDSFSALDYATDAALRAALARETAESTVVIVAQRVATIRDADRIIVLDEGRVVGTGRHEDLMAGNDTYREIVLSQLTEAEAA
>NZ_LN831790.1|WP_029385720.1|5589786_5591715_-|ABC-transporter-ATP-binding-protein
MAGPAARMMAGGGPDQRTMDFKGSGKRLLAQFKPERVTLWALLLCLVVSVGLSVVGPKILGRATDLVFAGIVGRDMPSGATKEQVLEGMRERGDDGVADMLRSTDFTPGRGIDFTAVGNVLLLALGTFLAAGLLMAVATRLVNRAVNRTVYRLREDVQTKLSRLPLSYFDKRQRGEVLSRATNDIDNMGQTLQQSMGQLINSLLTIIGVLAMMFYVSWILALVSLVTVPLSFVVATRVGKRSQPQFVQQWRTTGTLNAHIEEMYTGHTLVKVFGRQEESAQQFAEQNEALYEAGFKAQFNSGIMQPLMMFVSNLNYVLIAVVGGLRVATGSLSIGDVQAFIQYSRQFSTPLTQVASMANLVQSGVASAERIFELLDAEEQGPDPVPAEKPAELIGRVELERVSFRYDPDKPLIENLSLKVEPGHTVAIVGPTGAGKTTLVNLLMRFYEVSGGRITLDGVDIARMSRDELRAGIGMVLQDTWLFGGTIAENIAYGAAREVTRGEIEEAARAAHADRFIRTLPDGYDTVIDDEGSGVSAGEKQLITIARAFLSDPVILVLDEATSSVDTRTEVLIQKAMAKLAAGRTSFVIAHRLSTIRDADTILVMENGSIVEQGTHHDLLAAGGAYARLYRAQFAQAVVEMD
>NZ_LN831790.1|WP_176572968.1|5588453_5589620_+|sigma-70-family-RNA-polymerase-sigma-factor
MRHAVPHPKTRPETASGPAEGTGISGPFESPEAVAPVVPVAAVGPAGSAEPAEPGPDGLAEAVEPVDPVELVEPVEAPPARPEPGGPSSDLFRQYLREIGRIPLLTAAEEVELARRVEAGLFAEEKLNSTPDLDSRLAGDLDRLVVLGRMAKRQLIEANLRLVVSVAKRYVGRGLTMLDLVQEGNLGLIRAVEKFDYARGYKFSTYATWWIRQAMSRALADQARTIRVPVHVVELINRVVRVQRRMLQERGCEPTPAEVAAQLDLPPERVGEVLRLAQEPVSLHAPVGEEDDVALGDLIEDGDAASPVESAAFLLLREHLEAVLSTLGERERKVVQLRYGLVDGRPRTLEEIGRIFGVTRERIRQIESKTLGKLRDHTYAEQLRGYLH
>NZ_LN831790.1|WP_029385718.1|5586127_5588032_+|DNA-primase
MAGRINDEDVKAVRDAVPIDAVVSEYLQLRNAGGGNLKGLCPFHDEKSPSFQVSPAKGLFHCFGCQEGGDTITFVMKIDHLSFSEAVERLAAQAGITLRYEEGGYNPAHQRGERIRLVEAHKIAAEWYAEQLATSPEAETGRLFLAERGFDQAAAQHFSVGYSPQGWDHLTRYLRGKGFSDKELILSGLSQEGRRGPIDRFRGRLMWPIRDIGGEVVGFGARKLYEADTGPKYLNTPETAIYKKSQVLYGIDLAKKEIAKSSRAVVVEGYTDVMACHLAGVRTAIATCGTAFGGDHIKILRRLLMDNGSARVIFTFDGDAAGQKAALRAFEDDQKFAAETYIAIAPDGMDPCDLRLAKGDEAVADLVEPRTPLFEFALRQIVSRYDLDTPAGRAAALDEAAPVVARIKNSGAQHEVAVQLAGMLGILDTQFVVKRVAQLARWARDRGGKGPAPAPAPRQYAAAPGRPAPRGPALNLRNPVYATERELLKLALQRPELVSPAFDAYGVDEFTAPPYAAVRQAILDAGGAEPGVRDPQGYLVRVREAAPDDTVRAMVTELAVEAIMLRKEVDETYAGAQLVTVRRRAVERRIRDIQSQLTRLGTHGDPAQSAAVQNELWVLQQYDQALREHGAAAL
>NZ_LN831790.1|WP_063833346.1|5600219_5601092_-|cytochrome-c-oxidase-assembly-protein
MTAAGPLLLTALLTALLACAAYTAAAARLRRRGDAWPWWRQACCWLAGTVFVAGAALPWQTWLPPFTGHMAAHLAVGMVAPLPAVLARPVTLALRVLPVPGRRALLAVLHSRPAAVLACPPVAAALDIGGLWLLYRAPVPPQWHHSPWLYVHLFAAGWLFTFAVLAVDPLRHRTGLALRAGTLLAAAAAHAVLAKTLWAAGPPGTGYAPADLHRAAPLMYYGGDAVEIALAVALACQWYRAQGRALARRSRPARPHNPGRGGVPGPVPPERASRPLRPSDHRPRHQEASR
>NZ_LN831790.1|WP_047122049.1|5601147_5601618_-|DUF2243-domain-containing-protein
MTYRRAVAGGALLGIGLAAFVDEAVFHQLLHWHHFYDRSTPGAGLVSDGLLHAGSWLATVAGLFLYADLRRRGGPPRPAWWAGVCLGAGGFQLFDGLVDHKLLRVHQIRYGVDVTPYDWAWNAVAVLLLIAGLLLWRRARRAARSHHRGHLAGLRG
>NZ_LN831790.1|WP_029385730.1|5601614_5602184_-|hemerythrin-domain-containing-protein
MAGITASDADVVALLMRQHGDIRNLFDEVERTSGDERRAAFRRLVQLLAVHETAEEEVVHPFTRASVPDGGKIVDDRLAEEREAKEVLSRLDGMDPDDPKFLPGLLALRLDVMAHARAEERYEFNHIRRSADQARLASMATALRAAEAMAPTHPHPGTESAAKNMALGPIAAVMDRTRDAVRKAMGKDG
>NZ_LN831790.1|WP_029385731.1|5602185_5603388_-|hypothetical-protein
MGFNPLEHQGIPLDRQLRNWRELNVEPVDPDHGDPYTKCRVITMNGIEVEAILFSHQFARHCPDPEVKRQLAEVRYIEHQQQKAVNWLLPGLASVLETTIAYEQVAVDLTGWVARHEPDPYLKQAYEFGVLEDFDHLYRYANLYEMIEHRKAEAIVDGLTEVMPGRPTKFHHRNPVDNVREPYDRTKTDPISKLHALTIMSAEQQTMNFYMNVGPQYMEPIARQLYQEIGLIEEEHVTHYESLVDPGETWWEQLVNHEYNECYLYHSFMEQESDPKVKAVWELHLNMELEHLRIACDLMRRHDGREPAEILAPELPNVLTFEENKQFVRNLLDTQMDLTTLGTGYVRDAHERFERMQEQIHGGEEPPSERVMAQHREMFGREYRLETEGPHPDVASREKD
>NZ_LN831790.1|WP_029385732.1|5603506_5604223_-|ANTAR-domain-containing-protein
MTSAAPPRLAGRLTTLVIEARVDGHRALLAPRGELVHGCADVLAEALARLPAGIERVDLDMAGVAFMDTAGLQFLDVLNDHSHRRAVPVTATNWNGQPRRILELAGLDTTDPLHSTAHRPPCPRPGPGLAGVPASAPARSAVALERSERLHDLEAEVEQLRHAIASRPVIDQARGILMATHGCTSDEAWHLLRETSQVSNTKLRAVAAAITSSAGTGGPPLPAALRAALRTALARLRR
>NZ_LN831790.1|WP_047122050.1|5604449_5604818_+|STAS-domain-containing-protein
MGETKVGTQHEAPSRAAVAAPGLTVSPLTGRAGVRMAGEVGLSTRGIWEDALEQAVLEGEDVYYLELSGVTFADVAGVGALVAAAQRLPAGARFVLHRPPHVVQRVLELFWPGQPAIEVSMS
>NZ_LN831790.1|WP_078648339.1|5604814_5605846_+|sensor-histidine-kinase
MSAVAEPAESAESPRSPQSAEPATAPGSGPYSGAPEPTDPFVHPALFYRDDEEYLRGTVPFVREGLAAGEPVAVAVPGERLGLIRDALGDAADGVRMLDMREAGRNPGRIIPGVLRAFADAQPEGRRVRIIGEPIWAGRTDTEYPACVQHEALINAAFQGRTVTILCPYDAHRLDERVLADAYATHPTVIPAGPGPEQGSGAYAPDDVVARYNEPLAPPARALSFSFDADSLSHARHVATGEGERLGLTGVRLDDLALVSAELVTNSVVHGGGGGILRVWDEDGHVVCEVRDRGRLADPLAGRRPAAREQRGGRGLLLVNLVSDLVRVHTGPDGTTVRCWFAR
>NZ_LN831790.1|WP_029385735.1|5605864_5607352_-|GAF-domain-containing-protein
MTDAPRSRLALLLEAVLGVGTDLDPRGTLLRLVDGAAELTGAAHAWLSTTGPAPDVLTGISSPAAPPGVPDTPHRLRVPIHVEGEEFGALHLAGRAGGGPFTAADEQLLRFLAAQAGIAIANARLYGTARQRERWIEGAAAVTTALLTGDAAGDALTTVAKRARRLADAAAGVVLQPTGEGGMEIVAVSAPDDPGGLAGATIPPGSPVLEQLFAGEPVFVEDAATDPRMTTPVRHRFGPGMMLPLRAGGRLIGTLALPRRRGDRPYTGVERALAVQFASQAAVALVLADARRGRERLAVYEDRDRIARDLHDLVVQRLFATGLMLESTQRRTGAGDVEELVDRAVDDLRSTVREVRAAILALQRHPEPHRAGEHPAAPARGPAPAATVRDRVLRETAAAAARLGFAPSTRFTGAVDSRVPGPVADRLLGALRRALAAACGRPGVGRVEVTVDATATLPDGREAVRLTVRDDGGAGEDGGGTTVTWECAVRRAPPP
>NZ_LN831790.1|WP_029385736.1|5607372_5608410_-|rod-shape-determining-protein
MTASLEQLRRCHFAVDLGAARTRVYVKGAGLVVDQPSAAAVNTRTGALIAVGELAEKMTGRTPDFIRVVRPVSGGTVVDIEMAQRMLRHLLGDKIRRSLRRKPRLRAAACTPHDADPLARRATVETLVGLGARRVELVDILIAAAVGCGLPVERPEATMIMVCGAHATQVAVLSLGSIVTAERIPVGGEAVDYAIVQHLRHAHELMLPSQSVRPLQLALSGNGLTSNGPASTEIHGRDVATGLARSVQVDTAAVRDAIQTPLTTVLDGIGKVLRDCPPDLVADLADRGIMMVGGSALLPGFDQMLRQATGMPVHIAERPDICAVQGLGTMLEGKIEPLALNPLAG
>NZ_LN831790.1|WP_029385737.1|5608732_5612350_+|S8-family-serine-peptidase
MSRGPVGRGAALLSAGLLAGLLPVTPAAAREAPAGTSGTTPSAAHTVTLVTGDRVTVTDLGGGKRTVTVERPEGATGAVRTQEAGGRLSVVPDEALPYLRAGTLDERLFDVGALTEQGLADSRTGELPLIVTYDEGAPLLTPRGAERTRALPSVRGAAVRADKGREFWRAFTRQEGIDGVWLDGRVTARMAESNAQIGTPRAWEAGLTGKGVTVAVLDTGVDADHPDLAGRVAESRSFIEGEQVADRNGHGTHVASTVGGSGAASGGAERGVAPGARLAVGKVLSDQGSGSESQIIAGMEWAAREVKADVVSMSLGSPEASDGTDPMAQAVNTLSRETGALFVVAAGNTGTPSSIGSPGAADAALTVGAVDSADEAAYFTSAGPRSGDNALKPDLSAPGVGILAARSGLSEGSGDYTAMSGTSMATPHVAGVAALLAERHPDWTGAQLKDALMSTSKPLAASAYTLGAGRVSVPDAIGADVTATGSADFGFFSWPYEANEPVARTVTYTNHSGRDVEVSLAVRGAPEGVVTLADTTLTVPAHGTAATTVTGDGTGAPVGDTSGRIVASVGGTPVAHTAFGLVKEEERYTLTVHVKDRDGAATAADLTVQKLAAGADPVPARVGGSGTLRLRLTPGTYSLASFLDVRGSHGADSLGLGFLAAPEVVLDRDREVTLDGRALREIEAEPGRRTETRQLLMEYDRTANGSDLFEAVQVPLTYDSVFAAPTGKVTEGTFEYRTVWRLGKPLLEVKGVGEATVQAGGTLAEGRTRLPLVDAGDGPITGARGKAVLARLTDGTDPASLARAAQDAGAEALFVTDDAPGRLMAWWGTDDNADRPLTIATVNAADAARLREAGRVDMTGTRNTPYVYDLSEGHPGAIPDRDLTYRPGKRHLAVLHTKYHAAGPAAGGEFRYSITDTFPLAIGFKERIDFPAERTEYVSTGTGQGWHESVDVAGGALEQRRGLARYEGGSQTELNWFRPVWHPYLGTGLGWGQQRSGDVLRFNVPGWGDSGPDHTGFGDVYSEDSGMSQTTAIHRDGELVGRSADSTAHVWDAPAGEHTYRLVTDTALDADRWGTGTTGHAEWTFRSAATPEDRWTLLPLINLSFDVDTDLAGRVPAGRRLPVGVSAQYVQGAPDTGKLGGGRLEVSYDGGESWRPVALSGGAGASWRGTLTVPRDADSVSLRASARDDRGGSVTQEIVHAVGVR

Crispr_ID: NZ_LN831790_15

• CRISPR_ID: NZ_LN831790_15
• CRISPR_location: 7102609-7103300
• CRISPR_type: TypeI
• Repeat_type: NA
• Spacer_info: 9 spacers
• Cas_protein_info: cas3,cas5,cas8c,cas7,cas4,cas1,cas2

Consensus repeat of NZ_LN831790_15

Consensus_repeat	Method
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	PILER-CR
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CRISPRCasFinder
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACN	CRT

spacers of NZ_LN831790_15

>15.1|7102646|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
CCATACCCACCCTCAACACCCAGGAGCCCCACCCAT
>15.2|7102719|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
GTCGCTCCGGGGCGTCTCCCATGGGTGACCGTAAC
>15.3|7102791|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
ACGTCGACTGTGGCCCCGGCCCGGAGCCCACCGCCG
>15.4|7102864|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
CCGATCCCGGCGGGCAGGACAACCGTGCGGGCGGCG
>15.5|7102937|38|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
CGTCTGGACGCTGCGGGGGTGCGGGAGATCCTGCGCGG
>15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
ACTCCGCCCGCGGCCGCGAACCGCACCGACTCCCTC
>15.7|7103085|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
TCCCACCCTTCCTCGGCGCCGGTGTGCCACTCCCAG
>15.8|7103158|35|NZ_LN831790|CRT
CATTTCCATGCGGCGCCTTCGAGGTGCCAGAGCTG
>15.9|7103230|34|NZ_LN831790|CRT
CACACCACGTCGGTGGCCAGGGTGTGTTGGCCTC

CRISPR arrays and Neighbor proteins around NZ_LN831790_15

CRISPR arrays

The CRISPR arrays of NZ_LN831790_15

>merge|NZ_LN831790|15|7102609-7103300|PILER-CR,CRISPRCasFinder,CRT
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACCCATACCCACCCTCAACACCCAGGAGCCCCACCCATCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACGTCGCTCCGGGGCGTCTCCCATGGGTGACCGTAACCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACACGTCGACTGTGGCCCCGGCCCGGAGCCCACCGCCGCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACCCGATCCCGGCGGGCAGGACAACCGTGCGGGCGGCGCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACCGTCTGGACGCTGCGGGGGTGCGGGAGATCCTGCGCGGCTGGCGGTCGTCCCCCGGGGCGGCCGAGGATCGCAACACTCCGCCCGCGGCCGCGAACCGCACCGACTCCCTCCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACTCCCACCCTTCCTCGGCGCCGGTGTGCCACTCCCAGCTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAACCATTTCCATGCGGCGCCTTCGAGGTGCCAGAGCTGCTGGCGGTCGCTCCCGGGGCGACCGAGGATTGCAATGCACACCACGTCGGTGGCCAGGGTGTGTTGGCCTCCTGGCGGTTGCCTTAAGGGGCCGTTGATCGGTGAGTT

>NZ_LN831790|15|2|7102609-7103157|PILER-CR
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCATACCCACCCTCAACACCCAGGAGCCCCACCCAT
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	GTCGCTCCGGGGCGTCTCCCATGGGTGACCGTAAC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	ACGTCGACTGTGGCCCCGGCCCGGAGCCCACCGCCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCGATCCCGGCGGGCAGGACAACCGTGCGGGCGGCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CGTCTGGACGCTGCGGGGGTGCGGGAGATCCTGCGCGG
CTGGCGGTCGTCCCCCGGGGCGGCCGAGGATCGCAAC	ACTCCGCCCGCGGCCGCGAACCGCACCGACTCCCTC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	TCCCACCCTTCCTCGGCGCCGGTGTGCCACTCCCAG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC

>NZ_LN831790|15|15|7102609-7103157|CRISPRCasFinder
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCATACCCACCCTCAACACCCAGGAGCCCCACCCAT
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	GTCGCTCCGGGGCGTCTCCCATGGGTGACCGTAAC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	ACGTCGACTGTGGCCCCGGCCCGGAGCCCACCGCCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCGATCCCGGCGGGCAGGACAACCGTGCGGGCGGCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CGTCTGGACGCTGCGGGGGTGCGGGAGATCCTGCGCGG
CTGGCGGTCGTCCCCCGGGGCGGCCGAGGATCGCAAC	ACTCCGCCCGCGGCCGCGAACCGCACCGACTCCCTC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	TCCCACCCTTCCTCGGCGCCGGTGTGCCACTCCCAG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC

>NZ_LN831790|15|1|7102609-7103300|CRT
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCATACCCACCCTCAACACCCAGGAGCCCCACCCAT
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	GTCGCTCCGGGGCGTCTCCCATGGGTGACCGTAAC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	ACGTCGACTGTGGCCCCGGCCCGGAGCCCACCGCCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CCGATCCCGGCGGGCAGGACAACCGTGCGGGCGGCG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CGTCTGGACGCTGCGGGGGTGCGGGAGATCCTGCGCGG
CTGGCGGTCGTCCCCCGGGGCGGCCGAGGATCGCAAC	ACTCCGCCCGCGGCCGCGAACCGCACCGACTCCCTC
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	TCCCACCCTTCCTCGGCGCCGGTGTGCCACTCCCAG
CTGGCGGTCGTCCTCCGGGGCGGCCGAGGATCGCAAC	CATTTCCATGCGGCGCCTTCGAGGTGCCAGAGCTG
CTGGCGGTCGCTCCCGGGGCGACCGAGGATTGCAATG	CACACCACGTCGGTGGCCAGGGTGTGTTGGCCTC
CTGGCGGTTGCCTTAAGGGGCCGTTGATCGGTGAGTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|378245
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_LN831790.1|WP_029385483.1|7090463_7090898_-|hypothetical-protein	unknown	unknown	gnl|CDD|237057
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09651_cas5_CAS-I-C	gnl|CDD|187782
NZ_LN831790.1|WP_047122177.1|7091140_7092337_-|glycosyltransferase	unknown	unknown	gnl|CDD|213815
NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter	unknown	unknown	gnl|CDD|340927
NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379258
NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl|CDD|377458
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|187768
NZ_LN831790.1|WP_029385491.1|7095611_7096091_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|240032
NZ_LN831790.1|WP_029385489.1|7093932_7095543_+|apolipoprotein-N-acyltransferase	unknown	unknown	gnl|CDD|223885
NZ_LN831790.1|WP_029385486.1|7092376_7093162_+|aspartate/glutamate-racemase-family-protein	unknown	unknown	gnl|CDD|234851
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_LN831790.1|WP_029385488.1|7093267_7093813_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase	unknown	unknown	gnl|CDD|222853
NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein	unknown	unknown	gnl|CDD|222853
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	gnl|CDD|350688
NZ_LN831790.1|WP_029385493.1|7096145_7096946_+|3-hydroxybutyrate-dehydrogenase	unknown	unknown	gnl|CDD|211705
NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase	unknown	unknown	gnl|CDD|366690

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	1.5e-85	282.5	0.0
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	5.7e-22	72.5	0.0
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	2.2e-131	432.7	0.0
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09651_cas5_CAS-I-C	2.2e-66	218.2	0.0
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	2.8e-46	152.8	0.0
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	6.1e-88	289.4	0.0
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	3.7e-27	90.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|378245	pfam09709, Cas_Csd1, CRISPR-associated protein (Cas_Csd1). CRISPR loci appear to be mobile elements with a wide host range. This entry represents proteins that tend to be found near CRISPR repeats. The species range, so far, is exclusively bacterial and mesophilic, although CRISPR loci are particularly common among the archaea and thermophilic bacteria. Clusters of short DNA repeats with nonhomologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins.	1.57481e-97
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.40615e-22
NZ_LN831790.1|WP_029385483.1|7090463_7090898_-|hypothetical-protein	gnl|CDD|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	0.000112081
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|187782	cd09651, Cas5_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas5. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex; in subtype I-C this protein might be the endoribonuclease that generates crRNAs; also known as DevS family.	6.05152e-74
NZ_LN831790.1|WP_047122177.1|7091140_7092337_-|glycosyltransferase	gnl|CDD|213815	TIGR03469, HpnB, hopene-associated glycosyltransferase HpnB. This family of genes include a glycosyl transferase, group 2 domain (pfam00535) which are responsible, generally for the transfer of nucleotide-diphosphate sugars to substrates such as polysaccharides and lipids. The genes of this family are often found in the same genetic locus with squalene-hopene cyclase genes, and are never associated with genes for the metabolism of phytoene. Indeed, the members of this family appear to never be found in a genome lacking squalene-hopene cyclase (SHC), although not all genomes encoding SHC have this glycosyl transferase. In the organism Zymomonas mobilis the linkage of this gene to hopanoid biosynthesis has been noted and the gene named HpnB. Hopanoids are known to feature polar glycosyl head groups in many organisms.	4.07286e-158
NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter	gnl|CDD|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	0
NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	3.82561e-15
NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	7.78108e-05
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|377458	pfam05107, Cas_Cas7, CRISPR-associated protein Cas7. CRISPR-associated protein Cas7 is one of the components of the type I-B cascade-like antiviral defense complex. In Haloferax volcanii, Cas5, Cas6 and Cas7 form a small complex that aids the stability of CRISPR-derived RNA.	1.83061e-119
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	gnl|CDD|187768	cd09637, Cas4_I-A_I-B_I-C_I-D_II-B, CRISPR/Cas system-associated protein Cas4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas4 is RecB-like nuclease with three-cysteine C-terminal cluster.	3.65843e-27
NZ_LN831790.1|WP_029385491.1|7095611_7096091_+|NUDIX-domain-containing-protein	gnl|CDD|240032	cd04676, Nudix_Hydrolase_17, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	5.33356e-55
NZ_LN831790.1|WP_029385489.1|7093932_7095543_+|apolipoprotein-N-acyltransferase	gnl|CDD|223885	COG0815, Lnt, Apolipoprotein N-acyltransferase [Cell envelope biogenesis, outer membrane].	5.07893e-90
NZ_LN831790.1|WP_029385486.1|7092376_7093162_+|aspartate/glutamate-racemase-family-protein	gnl|CDD|234851	PRK00865, PRK00865, glutamate racemase; Provisional.	1.29575e-47
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	2.87784e-155
NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	1.06941e-48
NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	0.00268123
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	gnl|CDD|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	1.20339e-56
NZ_LN831790.1|WP_029385493.1|7096145_7096946_+|3-hydroxybutyrate-dehydrogenase	gnl|CDD|211705	TIGR01963, D-beta-hydroxybutyrate_dehydrogenase, 3-hydroxybutyrate dehydrogenase. This model represents a subfamily of the short chain dehydrogenases. Characterized members so far as 3-hydroxybutyrate dehydrogenases and are found in species that accumulate ester polmers called polyhydroxyalkanoic acids (PHAs) under certain conditions. Several members of the family are from species not known to accumulate PHAs, including Oceanobacillus iheyensis and Bacillus subtilis. However, polymer formation is not required for there be a role for 3-hydroxybutyrate dehydrogenase; it may be members of this family have the same function in those species.	1.58023e-122
NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase	gnl|CDD|366690	pfam01527, HTH_Tnp_1, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family consists of various E. coli insertion elements and other bacterial transposases some of which are members of the IS3 family.	1.42914e-10

Protein sequences

>NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein
MYTGIDEALAPPFSSAHIRATWNGTASVEDASRAFGFSRAKGYDLIRNGQFPCRVLRIGRKTRVVTASLLRVLESGVPEYNDARVGGHPTS
>NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter
MSSPATAPPAPSNLKRIVAASLIGTTIEWYDFFLYGSAAALVFNKLFFPDSDPLVGTLLSFLTYAVGFAARPLGALVFGHYGDRLGRKKLLVLSLLLMGGATFAIGLLPTHATIGTAAPVLLTVLRLVQGFALGGEWGGAVLLVSEHGDARRRGFWASWPQTGAPAGQLLATGVLSLLTALLSDEAFGDWGWRIPFLLSGVLVIVGLWIRLSVDESPVFQQALERAEAKSAQDERTPLVSVLRYHWRDVLVAMGARMAENISYYVITAFILVYATTSADVSKQTALNAVLIASAVHFAVIPAWGALSDRIGRRPVYLLGAAGVGLWMFPFFALIDTGEFGSLLLAVTVGLVLHGAMYAPQAAFFSEMFATRMRYSGASIGAQFASVAAGAPAPLIATALLSDYDSSTPISLYVIAAAVLTVVAVAAGKETRHRDLAEVASGAGTAPAASRKEDARAR
>NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein
MELLARGASADAYEQPVLLARAEGRPAERIAALEHAKLLALRVRSELEGRRRREAELSALFETAHDLAGLRDVDAVLRAIVQRARSLLGTDVAYLSLNDPARGDTYMRVTEGSVSARFQQLRLGMGEGLGGLVAQTARPYVTDDYFKDGRFQHTPTIDVAVRDEGLVAILGVPLMLGHHVIGVLFAADRRARVFEREQIALLGSFAALAAAAIDTANLLTETRSALAGLERANEIIRDRSAVIERASDVHDRLAELVLRGGGVHDVAAAVSEVLDGTVEFTEAGAAPADALEASRTEGHAVRHGDDWIAAVTAGGEQLGALVLRGHPGLDPVDQRTLERAAMVTSLLLLARRSAAEAEQRVRGELLDDLLDARDRDPRLLRDRARRLDADLGTTHTVLAARLDGPATDADQEADARRRLWAAASHLAATRHGLAAARDGGTVLLLPLGPAQTATEVARRTARHLGAAVHEAVTVGASAPVEDPAAHPDAVATAYAEARRCLEALRLLGRSGDGAAAEDFGFLGLLLAGDGDIAGFVHRTIGEVVAYDERRGTELLRTLEAYFACGMSPARTKNELHVHVNTVAQRLERVGRLLGDDWQSPARALEIQLALRLHRLSAPAPR
>NZ_LN831790.1|WP_029385493.1|7096145_7096946_+|3-hydroxybutyrate-dehydrogenase
MTSPSALPGPQAPALDLGGRTALVTGAAGGIGRACTLRLAAAGAKVRAVDRDAVGLEELAGHAGDLAGTVEPHVVDLTDLDAAELIAAGTDVLVNNAGLQLVRPLEDFPPDVFHTVLTVMLEAPFRLIRGALPHMYGQGWGRIVNVSSVHGLRASPYKAAYVAAKHGLEGLSKTAALEGAAHGVTSNCVNPGYVRTPLVEKQLIDQSRAHGLPEDRVLTDVLLRDSAVKRLIEPEEVAEAVAYLCGPQASFMTGASLVLDGGWTAH
>NZ_LN831790.1|WP_029385491.1|7095611_7096091_+|NUDIX-domain-containing-protein
MATPDFIRELRASAGHQLLWLPGVTALVFDDRGRVLLNRRSDTRRWSVIGGIPEPGEQPAACAVREVYEETAIRCAVERVVLVQALSPVTYDNGDVCQYMDITFRCRALGGEARVNDDESLEVGWFAVDALPDLHEFALFRIKQAMSDGPTWFDATDFG
>NZ_LN831790.1|WP_029385489.1|7093932_7095543_+|apolipoprotein-N-acyltransferase
MTVTATSVGEPDRLRSRTARAPRVPRLARLIPAVAAALSGALLYVSFPPRTLWWLAVPAFAVFGWVLRGGGWKAGLGLGYLFGLGFLLPLLVWTGVEVGPGPWLALVAIEAVFVALVGAGVAAVSRLPAAPVWAASLWTAGEAARARVPFEGFPWGKIAFGQADGVFLPLAAVGGTPLLGFAVVLCGFGLYDVVRLALRARRTRAVRRGTAAVALLSVAVPVAGALAARPLVTDEAEDGTATVAVVQGNVPRAGLDFNAQRRAVLDYHARETERLAAAVEAGEVARPDFVLWPENSSDIDPFANADARAVIDAAVRAIGAPISVGGVVERDGRLYNEQILWDPAKGPVDTYDKRQIQPFGEYLPLRSLIGAINSEWTSMVRQDFSRGDDPGVFTMDGTRVGLVTCYEAAFDWAVRSEVTDGAQMISVPSNNATFDRSEMTYQQLAMSRIRAVEHSRTVTVPVTSGVSAIILPDGRVTQKTGMFVPGSLVQEVPLRSSTTPATELGVLPEIALVLVAAGGLGRAIGAGVRGRRAGDV
>NZ_LN831790.1|WP_029385488.1|7093267_7093813_+|hypothetical-protein
MRDHRHGEHAPPPDVWTGRATNRVQWLLALIGAACLALGIALAVDSAWESGIAPLVMAVVGCIAAGLLVLFGTLAFVHVALRVDEECLEVRCGHIGVPRRRIPLSHVAGAEFAPHVTPRHWGGWGYRWRPEKGTAVVVRRGEGIVLRLWDGHTFTVTVDDAEAAVQVIKDRLRPKASGPAH
>NZ_LN831790.1|WP_029385486.1|7092376_7093162_+|aspartate/glutamate-racemase-family-protein
MKIALMDSGIGLLAATAAVRRLRPDADLVLSLDPDGMPWGPRTPEDLTERALAVAEAAAAHRPDALIVGCNTATVHALPTLRARLEPGIPVIGTVPAIKPAAAGGGPVAIWATPATTGSPYQRGLIRDFADGVPVAEVPCPGLADAVERADETAIDAAVAAAAARTPDGVTTVVLGCTHYELVAERIRAAVQRPGSPPLVLHGSAGAVAAQALRRIGARPEPGAPAEGGLTVLLSGRPGPLPAAALAYEEGRLLEAAAPAR
>NZ_LN831790.1|WP_047122177.1|7091140_7092337_-|glycosyltransferase
MGQTAHVSAVVWTAAVSLAAWVWLLLGQGFFWRTDVRLPPRREPAVWPPVCVVVPARDEAAVLPASLPSLLAQDYPGRAEVFLIDDGSSDGTAELARALARRHGGLPLTVDSPGGEPPAGWTGKLWALRHGIGLARARAPEYLLLTDADIAHAPDSLRHLVAAARTGGFDLVSQMARLRVRSRWERLVVPAFVYFFAQLYPFRRVGRKSARTAAAAGGCVLLRAEAADRARVPEAIRHAVIDDVALARAVKDGGGHIWLGLAERVDSVRPYPRLHDLWRMVSRSAYAQLRHHPLVLAGTVAGLALVYLVPPAALVAGAAAGDTAAAVLGGLAWLVMTGTYLPMLRYYRQPPWLAPLLPFTASLYLLMTVDSAVRHYRGRGAAWKGRTYARPDAVPDEG
>NZ_LN831790.1|WP_029385483.1|7090463_7090898_-|hypothetical-protein
MTSPRSTYGGGYYSASFRDTPIYDSLVAERGTPQIAPIRVPAAYDAPGSQLPALPSAMPALPAAPSQPVHGYPQQAPQHAPLQQAPAPYIPQQATAPRGYPGPQPPRPAAPAPAGYEAMRPAAPRPAPAPYQDPYYNQQQYGGY
>NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''
MAGVLYAHSLSGVSGVRHTLEDHLRGSAALARRFGEVFGAGELAEYLALVHDVGKGACAWQDGLRAVEARGGGGRVGVGHKHAGTVLAERYTQLACAAVVFGHHGGLPDLERLRDELHKGRPGGSEAARVQEAIRAVEGIVPEIHRSSRIALPGWLFDLPRREQRLGFDLLVRMLFSCVVDADYLDTSAHFTGAAVRVGEPVDMAALVERYEVRRKRYLAGRESSPVDALRQSVYERACAVAAGETGVYVLQVPTGGAKTMAAGAFALRHAAQHGKRRVVLAVPFISITEQNAAVYRDLLDPEDADGGSAVVLEHHSAVDLDLEGAGFGELAEEQREALRQRARTAKLAAENWDAPFVVTTTVRLFESLFSHRPSQMRRLHNLAGSVIVLDEVQALPDRLLAPILSGLRGLVDHFGATVLLVSATQPSFWELSAWKGLERKAVIDDPAALFDALRRVKYEWRTGQDVTLESIAREAATHPQVLTVVGTTRDAARFHRHLQAAFAQGVVLHLSTRMTGAHRREVIAQIRELLGRGEPVQVVSTSLIEAGVDVDFPRAYRAWAPPESLQQAAGRCNRDGRLPSGTVIVFDPADGGRPRSDEYRIAVQTGEQFFGPHPLVAPDDLDALHQYYQRRYSYQQGGDPEAGLGAHIEKLRRALDFPKVDREFQMIEDEHSVPVVVIRDEHDREQIEDAVAQLTDPSRPCGPEALRSLQQHTASLPKREADAALRCGLAVPVTGDLLLWHGAYHEQRGLDPDEPESLDTYGVV
>NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5
MAVRTAPASADRRGNGGWTFPDLVVEVSGPLACFTRPELKVERVSYPVMTPSAAVGVLEAIFWKPEMAYVITAIEVLKPIEWTKIRRNEVKSVISATEVAALRKTPGRRYDVENDRDQRNSMLLRDVHYRIRAQILRAPHAADVPEQKYRDQLRRRVDKGACFCEPYLGCREFSASFGPQTDARPIDRDEELGVMLHSIVHPVSGGEQYRWFHAQLHQGVMLVPVAPLGADKVAMPASSAWRADGSGTGR
>NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MLLHRLIEYAARAEADGELPPSYYRPKRIQWILQLNADGTEADFVSLREKPLETTAPYAYRSGTMPPPYLMVDTAQYVLALPKQAPGKPVTERAAEEGRRRRDAYADLLLAWADAAPDDPYAMVVRTFVTTGVLHRLEAPKEMTAADNIALVAHGNTWLHQLSSVREAWANSVRSRKSGKNAAGLCLVCGKEGELLSTIPESIKSGAIPTAGRGRDAQLVSINASAQGRGGALQLVNTPVCERCGGRAMAALNLLLTSDTNRRRATDSVTVWWTREPADDLFDTLDTPTDAVVARLLTSLHEHPDPATAERIDPNAYYALTLGLNNARAVVLDWLDIPVERLRNHLGAWFAHHRVYDGWNHTYRYFPLWRLALAAGRWDAKANKYAPGSAPKGLEQELLHAALTRDPVPARLLPYLLQRIRADRHVDPPRIALLRLALHPNRKDHQVTAPADRLDPAQLDPGYLCGRVFAVLEAIQYAALPDVKATIGDKFFGTAMTAPAAVIKTLRLGAAAHLKRLRRDNKAAYNALSRRLAEAFAAFDRHEGIPSMLTTEQQAKFVLGYEQQRAADFAAKAAHKKNKDQAAHDAAAEAG
>NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTSPHLDPNRKMDFVFLLEARDSNPNGDPDAGGMPRTDPVSGQGLITDVALKRKIRNTVALLNEEEKKPGYDIYVEAGVALNSQHERAYAADAAGSEASQMDAQQWMCRTFFDVRMFGAVMTTGQKNRQAGRVRGPVQLTFSRTVDPITPLELGITRVAPTKSEDLEKKTTEMGSKHIVPYGLYRGEGHFSAPLAGRTGVTSDDLAMFWRAFTLMFDHDRAAARGELNLRGLYVFTHDDKFGRAPARQLLDRVTVKGPGDATARAFSDYQVDVHQADLPEGVSLTTLIG
>NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4
MTVTSRQRGEADPAQVPLSALEHYTYCPRQCGLILLEDSFTDDAATVRGTLLHQRVDTPGNRGRGTVRTLHALPVWHDGHGLTGICDTVELHADGTVLPVEHKSGRYHPGGPADVQVAAQAMCLEYMFKQPVTTAAIYSGTDRRRHTVTVDEALRTRVLDATNAVRNLLSHNHTLPPPVADSRCRRCSMATDCMPKLLTGTHRYQQALHDLYLIDHTQDDDE
>NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MTTELLNTLYVQTQGTDLRLDQDTLRIHLPDTPGRRTLPLRRLNGIVVYGHVNLSTELITRCAQDRRPITWMSRGGRYLARLDGAVHGNVLLRHAQHQRYNDTDTRLGIARNIVAGKIRNSRWILLRAARDAAPARRKHIRNAAKDLAEAIDKLGAAESIDIVMGTEGQAARNYFAALPHILSPTTDLPPFTHRNRRPPTDPVNAALSFTYGLLRSLVHGAVEQVGLDPYLGFLHGLRPGKPALALDLMEEFRPVLADRFTLTQFNRRQLRASHFNHLSGGAVSLTDDGRKELIAAWQEWKTQTWDHPIAGRAVPAGLLPVIQARLLARHLRGEFPGYLPWTAA
>NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2
MDLLLTYDVDTTSPAGQRRLRRVAKLCECHGLRVQKSVFEIVADEKTLLTLLHALDQIIDSDTDSIRLYRLPADGFDHVQTLGIAQIQPHRGDLVL
>NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase
MHAELRRLGRRVNRKRVARVMRERDIRGATRRRRCSLTRPDAKAKPAPDLIGRDFHAGHPGTKLVGDITCLPTAEGRLYLACWLDLATREVVGYAMADHHRAEIVVDALDMAHGRGGLETGCVIHSDRGSEYTSTRFRERIRELGLRQSCGRTGSCFDNAAAESFWALLKEEIGTRTWPDRATARAEVFSFIETFYNRRRLRKHRTFGYLTPAETRQRHQHTLAA
>NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein
MSELYRLIHAEKATYPIVLLCRVLKVARSSYYAWREGEHARAARRAADDALAHEIAVLHIASRHTYGVRVSTPNCGAWAGG
>NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase
MGSKYTKRYTEEFKRDAIALVDSSGKTVTAVARELGISSESLRGWYRRAKADRGVGESGELTSAEREELKRLRREVREQQQTIEILKKATAFFVKENDR

Crispr_ID: NZ_LN831790_16

• CRISPR_ID: NZ_LN831790_16
• CRISPR_location: 7112194-7113102
• CRISPR_type: TypeI
• Repeat_type: NA
• Spacer_info: 12 spacers
• Cas_protein_info: cas2,cas1,cas4,cas7,cas8c,cas5,cas3

Consensus repeat of NZ_LN831790_16

Consensus_repeat	Method
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	PILER-CR
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CRISPRCasFinder
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CRT

spacers of NZ_LN831790_16

>16.1|7112231|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
TTGTCGCGCTGCGACCGGACCTCGGCCGGGATCTGG
>16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
AGCGCGCGGGTGAAGATCGGCATCACGGCCGGCTG
>16.3|7112376|38|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
TCCACCGACGAGATCACTCGCGTCTCCAACCGGGGGGG
>16.4|7112451|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
CCTCCGCACAGTCGTACGATGGCGAGCGTGAGCA
>16.5|7112522|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
CTGTTCTCCGCCGACCGCGCCCACACCGATCTGGGC
>16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
AACGACGAGACGCTGCGCAAGGCGGCCGAGCTCGC
>16.7|7112667|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
GACGTGCCGGGCTGTGTGGTCGCGCCGCGGGAGCAG
>16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
ATGTGGCTGGACACGGACGGCTCCCAGCTGGCGG
>16.9|7112811|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
ACCGCCGGGTGGGCCGTGCTCTCCGACACCAACGGC
>16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT
GACGACTCGGGCACCGTCGCCGGGATCGTCACCG
>16.11|7112955|36|NZ_LN831790|CRISPRCasFinder,CRT
TACGTAGGTGGCGCCTGCGTCGCGGATGATGGTTGC
>16.12|7113028|38|NZ_LN831790|CRISPRCasFinder,CRT
CACTCCGGGACCACGGCATCCGGGTACACGACGTCCAA

CRISPR arrays and Neighbor proteins around NZ_LN831790_16

CRISPR arrays

The CRISPR arrays of NZ_LN831790_16

>merge|NZ_LN831790|16|7112194-7113102|PILER-CR,CRISPRCasFinder,CRT
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACTTGTCGCGCTGCGACCGGACCTCGGCCGGGATCTGGGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACAGCGCGCGGGTGAAGATCGGCATCACGGCCGGCTGGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACTCCACCGACGAGATCACTCGCGTCTCCAACCGGGGGGGGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACCCTCCGCACAGTCGTACGATGGCGAGCGTGAGCAGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACCTGTTCTCCGCCGACCGCGCCCACACCGATCTGGGCGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACAACGACGAGACGCTGCGCAAGGCGGCCGAGCTCGCGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACGACGTGCCGGGCTGTGTGGTCGCGCCGCGGGAGCAGGTGGCGGTTGTCCTCCGGGACGGCCGAGGATCGCAACATGTGGCTGGACACGGACGGCTCCCAGCTGGCGGGTGGCGGTCGTGCTCCGGGACGGCCGAGGATCGCAACACCGCCGGGTGGGCCGTGCTCTCCGACACCAACGGCGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACGACGACTCGGGCACCGTCGCCGGGATCGTCACCGGTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAACTACGTAGGTGGCGCCTGCGTCGCGGATGATGGTTGCCTGGCGGTCGCCCTTCGGGGCGGCCGAGGATCGCAACCACTCCGGGACCACGGCATCCGGGTACACGACGTCCAACTGGCGGTCGCCCTCCGGTGCGGCCGAGGATCGCAAC

>NZ_LN831790|16|3|7112194-7112954|PILER-CR
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TTGTCGCGCTGCGACCGGACCTCGGCCGGGATCTGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AGCGCGCGGGTGAAGATCGGCATCACGGCCGGCTG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TCCACCGACGAGATCACTCGCGTCTCCAACCGGGGGGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CCTCCGCACAGTCGTACGATGGCGAGCGTGAGCA
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CTGTTCTCCGCCGACCGCGCCCACACCGATCTGGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AACGACGAGACGCTGCGCAAGGCGGCCGAGCTCGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGTGCCGGGCTGTGTGGTCGCGCCGCGGGAGCAG
GTGGCGGTTGTCCTCCGGGACGGCCGAGGATCGCAAC	ATGTGGCTGGACACGGACGGCTCCCAGCTGGCGG
GTGGCGGTCGTGCTCCGGGACGGCCGAGGATCGCAAC	ACCGCCGGGTGGGCCGTGCTCTCCGACACCAACGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGACTCGGGCACCGTCGCCGGGATCGTCACCG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC

>NZ_LN831790|16|16|7112194-7113102|CRISPRCasFinder
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TTGTCGCGCTGCGACCGGACCTCGGCCGGGATCTGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AGCGCGCGGGTGAAGATCGGCATCACGGCCGGCTG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TCCACCGACGAGATCACTCGCGTCTCCAACCGGGGGGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CCTCCGCACAGTCGTACGATGGCGAGCGTGAGCA
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CTGTTCTCCGCCGACCGCGCCCACACCGATCTGGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AACGACGAGACGCTGCGCAAGGCGGCCGAGCTCGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGTGCCGGGCTGTGTGGTCGCGCCGCGGGAGCAG
GTGGCGGTTGTCCTCCGGGACGGCCGAGGATCGCAAC	ATGTGGCTGGACACGGACGGCTCCCAGCTGGCGG
GTGGCGGTCGTGCTCCGGGACGGCCGAGGATCGCAAC	ACCGCCGGGTGGGCCGTGCTCTCCGACACCAACGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGACTCGGGCACCGTCGCCGGGATCGTCACCG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TACGTAGGTGGCGCCTGCGTCGCGGATGATGGTTGC
CTGGCGGTCGCCCTTCGGGGCGGCCGAGGATCGCAAC	CACTCCGGGACCACGGCATCCGGGTACACGACGTCCAA
CTGGCGGTCGCCCTCCGGTGCGGCCGAGGATCGCAAC

>NZ_LN831790|16|2|7112194-7113102|CRT
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TTGTCGCGCTGCGACCGGACCTCGGCCGGGATCTGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AGCGCGCGGGTGAAGATCGGCATCACGGCCGGCTG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TCCACCGACGAGATCACTCGCGTCTCCAACCGGGGGGG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CCTCCGCACAGTCGTACGATGGCGAGCGTGAGCA
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	CTGTTCTCCGCCGACCGCGCCCACACCGATCTGGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	AACGACGAGACGCTGCGCAAGGCGGCCGAGCTCGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGTGCCGGGCTGTGTGGTCGCGCCGCGGGAGCAG
GTGGCGGTTGTCCTCCGGGACGGCCGAGGATCGCAAC	ATGTGGCTGGACACGGACGGCTCCCAGCTGGCGG
GTGGCGGTCGTGCTCCGGGACGGCCGAGGATCGCAAC	ACCGCCGGGTGGGCCGTGCTCTCCGACACCAACGGC
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	GACGACTCGGGCACCGTCGCCGGGATCGTCACCG
GTGGCGGTCGTCCTCCGGGACGGCCGAGGATCGCAAC	TACGTAGGTGGCGCCTGCGTCGCGGATGATGGTTGC
CTGGCGGTCGCCCTTCGGGGCGGCCGAGGATCGCAAC	CACTCCGGGACCACGGCATCCGGGTACACGACGTCCAA
CTGGCGGTCGCCCTCCGGTGCGGCCGAGGATCGCAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl|CDD|377458
NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein	unknown	unknown	gnl|CDD|222853
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09651_cas5_CAS-I-C	gnl|CDD|187782
NZ_LN831790.1|WP_029384415.1|7121464_7122775_+|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter	unknown	unknown	gnl|CDD|340927
NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379258
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|378245
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|187768
NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase	unknown	unknown	gnl|CDD|366690
NZ_LN831790.1|WP_029384407.1|7116449_7117370_-|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831790.1|WP_049976818.1|7120054_7121389_+|MFS-transporter	unknown	unknown	gnl|CDD|225121
NZ_LN831790.1|WP_029384410.1|7117366_7118431_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_LN831790.1|WP_029384412.1|7118543_7119812_+|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase	unknown	unknown	gnl|CDD|222853
NZ_LN831790.1|WP_078648264.1|7114228_7114954_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224715
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	gnl|CDD|350688
NZ_LN831790.1|WP_029384405.1|7114893_7116429_-|GMC-family-oxidoreductase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|274143

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	6.1e-88	289.4	0.0
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	2.8e-46	152.8	0.0
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09651_cas5_CAS-I-C	2.2e-66	218.2	0.0
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	2.2e-131	432.7	0.0
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	5.7e-22	72.5	0.0
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	1.5e-85	282.5	0.0
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	3.7e-27	90.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|377458	pfam05107, Cas_Cas7, CRISPR-associated protein Cas7. CRISPR-associated protein Cas7 is one of the components of the type I-B cascade-like antiviral defense complex. In Haloferax volcanii, Cas5, Cas6 and Cas7 form a small complex that aids the stability of CRISPR-derived RNA.	1.83061e-119
NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	7.78108e-05
NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	0.00268123
NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|187782	cd09651, Cas5_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas5. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex; in subtype I-C this protein might be the endoribonuclease that generates crRNAs; also known as DevS family.	6.05152e-74
NZ_LN831790.1|WP_029384415.1|7121464_7122775_+|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.41819e-16
NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter	gnl|CDD|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	0
NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	3.82561e-15
NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.40615e-22
NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|378245	pfam09709, Cas_Csd1, CRISPR-associated protein (Cas_Csd1). CRISPR loci appear to be mobile elements with a wide host range. This entry represents proteins that tend to be found near CRISPR repeats. The species range, so far, is exclusively bacterial and mesophilic, although CRISPR loci are particularly common among the archaea and thermophilic bacteria. Clusters of short DNA repeats with nonhomologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins.	1.57481e-97
NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4	gnl|CDD|187768	cd09637, Cas4_I-A_I-B_I-C_I-D_II-B, CRISPR/Cas system-associated protein Cas4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas4 is RecB-like nuclease with three-cysteine C-terminal cluster.	3.65843e-27
NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase	gnl|CDD|366690	pfam01527, HTH_Tnp_1, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family consists of various E. coli insertion elements and other bacterial transposases some of which are members of the IS3 family.	1.42914e-10
NZ_LN831790.1|WP_029384407.1|7116449_7117370_-|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	2.59042e-39
NZ_LN831790.1|WP_049976818.1|7120054_7121389_+|MFS-transporter	gnl|CDD|225121	COG2211, MelB, Na+/melibiose symporter and related transporters [Carbohydrate transport and metabolism].	1.25277e-104
NZ_LN831790.1|WP_029384410.1|7117366_7118431_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	4.92561e-53
NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	2.87784e-155
NZ_LN831790.1|WP_029384412.1|7118543_7119812_+|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	1.82488e-51
NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	1.06941e-48
NZ_LN831790.1|WP_078648264.1|7114228_7114954_+|GntR-family-transcriptional-regulator	gnl|CDD|224715	COG1802, GntR, Transcriptional regulators [Transcription].	8.20404e-18
NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''	gnl|CDD|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	1.20339e-56
NZ_LN831790.1|WP_029384405.1|7114893_7116429_-|GMC-family-oxidoreductase-N-terminal-domain-containing-protein	gnl|CDD|274143	TIGR02462, Pyranose_2-oxidase, pyranose oxidase. Pyranose oxidase (also called glucose 2-oxidase) converts D-glucose and molecular oxygen to 2-dehydro-D-glucose and hydrogen peroxide. Peroxide production is believed to be important to the wood rot fungi in which this enzyme is found for lignin degradation.	5.26164e-63

Protein sequences

>NZ_LN831790.1|WP_029384400.1|7111713_7112004_+|CRISPR-associated-endonuclease-Cas2
MDLLLTYDVDTTSPAGQRRLRRVAKLCECHGLRVQKSVFEIVADEKTLLTLLHALDQIIDSDTDSIRLYRLPADGFDHVQTLGIAQIQPHRGDLVL
>NZ_LN831790.1|WP_029384398.1|7110679_7111714_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MTTELLNTLYVQTQGTDLRLDQDTLRIHLPDTPGRRTLPLRRLNGIVVYGHVNLSTELITRCAQDRRPITWMSRGGRYLARLDGAVHGNVLLRHAQHQRYNDTDTRLGIARNIVAGKIRNSRWILLRAARDAAPARRKHIRNAAKDLAEAIDKLGAAESIDIVMGTEGQAARNYFAALPHILSPTTDLPPFTHRNRRPPTDPVNAALSFTYGLLRSLVHGAVEQVGLDPYLGFLHGLRPGKPALALDLMEEFRPVLADRFTLTQFNRRQLRASHFNHLSGGAVSLTDDGRKELIAAWQEWKTQTWDHPIAGRAVPAGLLPVIQARLLARHLRGEFPGYLPWTAA
>NZ_LN831790.1|WP_029384397.1|7110014_7110683_+|CRISPR-associated-protein-Cas4
MTVTSRQRGEADPAQVPLSALEHYTYCPRQCGLILLEDSFTDDAATVRGTLLHQRVDTPGNRGRGTVRTLHALPVWHDGHGLTGICDTVELHADGTVLPVEHKSGRYHPGGPADVQVAAQAMCLEYMFKQPVTTAAIYSGTDRRRHTVTVDEALRTRVLDATNAVRNLLSHNHTLPPPVADSRCRRCSMATDCMPKLLTGTHRYQQALHDLYLIDHTQDDDE
>NZ_LN831790.1|WP_029384395.1|7109148_7110018_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTSPHLDPNRKMDFVFLLEARDSNPNGDPDAGGMPRTDPVSGQGLITDVALKRKIRNTVALLNEEEKKPGYDIYVEAGVALNSQHERAYAADAAGSEASQMDAQQWMCRTFFDVRMFGAVMTTGQKNRQAGRVRGPVQLTFSRTVDPITPLELGITRVAPTKSEDLEKKTTEMGSKHIVPYGLYRGEGHFSAPLAGRTGVTSDDLAMFWRAFTLMFDHDRAAARGELNLRGLYVFTHDDKFGRAPARQLLDRVTVKGPGDATARAFSDYQVDVHQADLPEGVSLTTLIG
>NZ_LN831790.1|WP_047122179.1|7107263_7109039_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MLLHRLIEYAARAEADGELPPSYYRPKRIQWILQLNADGTEADFVSLREKPLETTAPYAYRSGTMPPPYLMVDTAQYVLALPKQAPGKPVTERAAEEGRRRRDAYADLLLAWADAAPDDPYAMVVRTFVTTGVLHRLEAPKEMTAADNIALVAHGNTWLHQLSSVREAWANSVRSRKSGKNAAGLCLVCGKEGELLSTIPESIKSGAIPTAGRGRDAQLVSINASAQGRGGALQLVNTPVCERCGGRAMAALNLLLTSDTNRRRATDSVTVWWTREPADDLFDTLDTPTDAVVARLLTSLHEHPDPATAERIDPNAYYALTLGLNNARAVVLDWLDIPVERLRNHLGAWFAHHRVYDGWNHTYRYFPLWRLALAAGRWDAKANKYAPGSAPKGLEQELLHAALTRDPVPARLLPYLLQRIRADRHVDPPRIALLRLALHPNRKDHQVTAPADRLDPAQLDPGYLCGRVFAVLEAIQYAALPDVKATIGDKFFGTAMTAPAAVIKTLRLGAAAHLKRLRRDNKAAYNALSRRLAEAFAAFDRHEGIPSMLTTEQQAKFVLGYEQQRAADFAAKAAHKKNKDQAAHDAAAEAG
>NZ_LN831790.1|WP_029384392.1|7106503_7107256_+|type-I-C-CRISPR-associated-protein-Cas5
MAVRTAPASADRRGNGGWTFPDLVVEVSGPLACFTRPELKVERVSYPVMTPSAAVGVLEAIFWKPEMAYVITAIEVLKPIEWTKIRRNEVKSVISATEVAALRKTPGRRYDVENDRDQRNSMLLRDVHYRIRAQILRAPHAADVPEQKYRDQLRRRVDKGACFCEPYLGCREFSASFGPQTDARPIDRDEELGVMLHSIVHPVSGGEQYRWFHAQLHQGVMLVPVAPLGADKVAMPASSAWRADGSGTGR
>NZ_LN831790.1|WP_164497185.1|7103540_7105838_+|CRISPR-associated-endonuclease-Cas3''
MAGVLYAHSLSGVSGVRHTLEDHLRGSAALARRFGEVFGAGELAEYLALVHDVGKGACAWQDGLRAVEARGGGGRVGVGHKHAGTVLAERYTQLACAAVVFGHHGGLPDLERLRDELHKGRPGGSEAARVQEAIRAVEGIVPEIHRSSRIALPGWLFDLPRREQRLGFDLLVRMLFSCVVDADYLDTSAHFTGAAVRVGEPVDMAALVERYEVRRKRYLAGRESSPVDALRQSVYERACAVAAGETGVYVLQVPTGGAKTMAAGAFALRHAAQHGKRRVVLAVPFISITEQNAAVYRDLLDPEDADGGSAVVLEHHSAVDLDLEGAGFGELAEEQREALRQRARTAKLAAENWDAPFVVTTTVRLFESLFSHRPSQMRRLHNLAGSVIVLDEVQALPDRLLAPILSGLRGLVDHFGATVLLVSATQPSFWELSAWKGLERKAVIDDPAALFDALRRVKYEWRTGQDVTLESIAREAATHPQVLTVVGTTRDAARFHRHLQAAFAQGVVLHLSTRMTGAHRREVIAQIRELLGRGEPVQVVSTSLIEAGVDVDFPRAYRAWAPPESLQQAAGRCNRDGRLPSGTVIVFDPADGGRPRSDEYRIAVQTGEQFFGPHPLVAPDDLDALHQYYQRRYSYQQGGDPEAGLGAHIEKLRRALDFPKVDREFQMIEDEHSVPVVVIRDEHDREQIEDAVAQLTDPSRPCGPEALRSLQQHTASLPKREADAALRCGLAVPVTGDLLLWHGAYHEQRGLDPDEPESLDTYGVV
>NZ_LN831790.1|WP_107409013.1|7101284_7101560_-|helix-turn-helix-domain-containing-protein
MYTGIDEALAPPFSSAHIRATWNGTASVEDASRAFGFSRAKGYDLIRNGQFPCRVLRIGRKTRVVTASLLRVLESGVPEYNDARVGGHPTS
>NZ_LN831790.1|WP_047122178.1|7099168_7100542_-|MHS-family-MFS-transporter
MSSPATAPPAPSNLKRIVAASLIGTTIEWYDFFLYGSAAALVFNKLFFPDSDPLVGTLLSFLTYAVGFAARPLGALVFGHYGDRLGRKKLLVLSLLLMGGATFAIGLLPTHATIGTAAPVLLTVLRLVQGFALGGEWGGAVLLVSEHGDARRRGFWASWPQTGAPAGQLLATGVLSLLTALLSDEAFGDWGWRIPFLLSGVLVIVGLWIRLSVDESPVFQQALERAEAKSAQDERTPLVSVLRYHWRDVLVAMGARMAENISYYVITAFILVYATTSADVSKQTALNAVLIASAVHFAVIPAWGALSDRIGRRPVYLLGAAGVGLWMFPFFALIDTGEFGSLLLAVTVGLVLHGAMYAPQAAFFSEMFATRMRYSGASIGAQFASVAAGAPAPLIATALLSDYDSSTPISLYVIAAAVLTVVAVAAGKETRHRDLAEVASGAGTAPAASRKEDARAR
>NZ_LN831790.1|WP_047122711.1|7097259_7099125_+|helix-turn-helix-domain-containing-protein
MELLARGASADAYEQPVLLARAEGRPAERIAALEHAKLLALRVRSELEGRRRREAELSALFETAHDLAGLRDVDAVLRAIVQRARSLLGTDVAYLSLNDPARGDTYMRVTEGSVSARFQQLRLGMGEGLGGLVAQTARPYVTDDYFKDGRFQHTPTIDVAVRDEGLVAILGVPLMLGHHVIGVLFAADRRARVFEREQIALLGSFAALAAAAIDTANLLTETRSALAGLERANEIIRDRSAVIERASDVHDRLAELVLRGGGVHDVAAAVSEVLDGTVEFTEAGAAPADALEASRTEGHAVRHGDDWIAAVTAGGEQLGALVLRGHPGLDPVDQRTLERAAMVTSLLLLARRSAAEAEQRVRGELLDDLLDARDRDPRLLRDRARRLDADLGTTHTVLAARLDGPATDADQEADARRRLWAAASHLAATRHGLAAARDGGTVLLLPLGPAQTATEVARRTARHLGAAVHEAVTVGASAPVEDPAAHPDAVATAYAEARRCLEALRLLGRSGDGAAAEDFGFLGLLLAGDGDIAGFVHRTIGEVVAYDERRGTELLRTLEAYFACGMSPARTKNELHVHVNTVAQRLERVGRLLGDDWQSPARALEIQLALRLHRLSAPAPR
>NZ_LN831790.1|WP_104532216.1|7113155_7113833_-|IS3-family-transposase
MHAELRRLGRRVNRKRVARVMRERDIRGATRRRRCSLTRPDAKAKPAPDLIGRDFHAGHPGTKLVGDITCLPTAEGRLYLACWLDLATREVVGYAMADHHRAEIVVDALDMAHGRGGLETGCVIHSDRGSEYTSTRFRERIRELGLRQSCGRTGSCFDNAAAESFWALLKEEIGTRTWPDRATARAEVFSFIETFYNRRRLRKHRTFGYLTPAETRQRHQHTLAA
>NZ_LN831790.1|WP_078648258.1|7113796_7114042_-|hypothetical-protein
MSELYRLIHAEKATYPIVLLCRVLKVARSSYYAWREGEHARAARRAADDALAHEIAVLHIASRHTYGVRVSTPNCGAWAGG
>NZ_LN831790.1|WP_029384401.1|7114038_7114338_-|transposase
MGSKYTKRYTEEFKRDAIALVDSSGKTVTAVARELGISSESLRGWYRRAKADRGVGESGELTSAEREELKRLRREVREQQQTIEILKKATAFFVKENDR
>NZ_LN831790.1|WP_078648264.1|7114228_7114954_+|GntR-family-transcriptional-regulator
MPSSRATAVTVLPEESTSAIASRLNSSVYRFVYLLPTWCYFLWNLKIPVSRCPRSRGSFTRRYDLTPGQLAHLLRRIAVEGWIERLPGYGWEFQPMLTSMDAYQDSYRFRLTIEPAALLEPGFVLDREALETARAQQRRLVDGDIRTIGNAQLYDLNSRFHEAVMACSRNTFFIDALRRVDRLRRLMEYRRSLQRDRALVRCAEHVEIADLLLAGKRAEASAYLREHLSSVGVEKASRPDG
>NZ_LN831790.1|WP_029384405.1|7114893_7116429_-|GMC-family-oxidoreductase-N-terminal-domain-containing-protein
MSLPSATAYDLVVVGSGPTGSTYVREVYDRHPTARVLLLDAGPRLTDPPGAHVKNIPDAGERARAQRASEGPGPAGRPGTRLLGAPDLPAAALSTNVGGMGVHWTGACPRPGDGERVPFVPAAEMDSHLARAEQLLHVDAHAFDHAPFADEVRARLSALFDPGRPEDRRVAAMPLAVTRRPDGAHAWSGTDVVLGRAAHDLRVEIADRCLCLRVELDAGAVTGVTVRDLADGGERTVTARAVVVAADALRTPQLLHASGIRPPALGRYLNDQPQIVHAARLPDDVVTAHHAVTGRTRDEDGAIVPQSGVSWVPYTDAHPFHGQVMQLDASPVPLADDTTVEPGTVVGLGWFCAKDITAEDRVEFDDNTADAYGLPAMRVHYRYTERDLATIEQAKKAVTEAAAAVGVPLDDSPVLLPAGSSLHYQGTTRMGPADDGTSVCDSHSRVWGTQGLWVAGNNVIPTATACNPTLTSVALAVRGAAALLDHLRPPADQPSGRLAFSTPTEDRCSRR
>NZ_LN831790.1|WP_029384407.1|7116449_7117370_-|sugar-phosphate-isomerase/epimerase
MRLGMLTACLPTWPLERVAGWAARAGYECLEVAVWPDTGGRDFEAAHIDVARFDARERERVRRSTEEKGLTISALAYYENNLHPDPARRREIRSHLEHAVDAAQALGVPYVGTFIGRDPARSVPENQREAERVLPGLVEYAGERDVKLIIENCVMEGWHPDGHPGNIAYSPELWEWMFSLGLYLNWDPSHLMWLGIDPLATITPYADRIVHAQAKDIELDPVARNRYGFFGTTAKDGDPWATGWWRYRVPGRGQVDWTRVVDRLYEAGFTGTLSVEHEDPLWGGTPEKVCQGLAIAHHTLRPLVVA
>NZ_LN831790.1|WP_029384410.1|7117366_7118431_-|Gfo/Idh/MocA-family-oxidoreductase
MQQIQAAVVGTGFMGSVHARAVTAAAGRVRLVAGRTPEGARDLADAVPGAVPATFEEVLASDVDVVHLCTPNHLHHDMARQALEAGKHVVCEKPLAVSVKEAEDLADFAARTGRVATVPFVYRFYASVRLARSLIGAEARGPWLLHGSYLQDWLADADADNWRVDADRGGDSRTFGDIGIHWCDLMEFVTGQRITAVQATLGRAHPVRAGREVSTEDGGVISFRTDTGGLGSLVISQASAGRKNRLWFSFDGPEASYVFDQENPERLWVGGRDADRVLTRDPAHAGGRPDALPPGHPQGYRECFADFVSDTYAAARGESVDGLPTFDAGLRAARLTRAVLDSAAADSTWTEVPA
>NZ_LN831790.1|WP_029384412.1|7118543_7119812_+|ROK-family-protein
MSRRPPTAIDQYEALSTVLRLVRGDRARTRPELGATALLGRTVISQRVEEAMGLGLLEDADIGPSNGGRAPRRLRFRAEQGLVLCAVLGAAALDVAVTDLDGRVLDRRHLEWRIARGPEQTLDFLDEQFTGLLEDRDPERLWAVVIGVPGPVEFATGRPSQPPIMPGWDGYDIRGRLQRRWGVPVWVDNDANLLALGEARTTGLADDQHLIFVKAGTGIGAGIVSRGRIHRGSKGAAGDIGHARVQEDNSTMCRCGRTGCLEALAGGWALARDAVGAVHEGRSRFLADIHRATGEITPADIGRGVVAGDAWCLTAVARAAERIGSLMAALVNFYDPDCLVFGGGAVTGSDTFLRVVDHTVRSRALPLASEGLTIRSSVAGDTGVVGGAHLAVEALLSADALAAWAPGGSPSAVAPERLVAGA
>NZ_LN831790.1|WP_049976818.1|7120054_7121389_+|MFS-transporter
MPSPAAGVATGPSAEPRPLPRTAQFGYGLGDLASNLTWTTLTAFLLFFYTDVAALTAATAGTILLIGRIADAVIDPLVGLAVDRTRSRFGRARPYLIFGAPVLGIAFALAFTAPGTGTTAVVWAAVTFVVVGVCHSLVNVPYGAMLPMLTDDTDTRLKMSGYRFVGASLGLITVSLAVMPLVEILGGTDRAGGFTGMAIVLGAAGTLLYWVVALLCRERPAPPVAREATSLHALASLPRNRHWLGVSAASLAAFVRLGIITAGAVYYARDVLDDTWATSYILLAFSLSALVGSLVTPWFLRRTGKRRGITVGLAATAALYVLLFFLDGRPVLFLAVFLLANLFGGFGLVAAPALVSDAIDHHETLTGRRDEGLLYAGYSFATKVGTALGGSLFAWALAWGGYRAEHVSAQASQAIEWAFIGLPAVLCLVQAACMRLYDLERRHA
>NZ_LN831790.1|WP_029384415.1|7121464_7122775_+|sugar-phosphate-isomerase/epimerase
MLERPIIQQRGFRNTTDGAGAEGFQLQLRNPNYRGIAGSLVDGADVIVDGRTFPREAQRWTLGGRTFTLDELRASTDVRWQLDEPATLFVPHPGGLSAGVHHIEVAVHLRRPYIPEIAGPSVFRSTATATIVPDPAANGGLRYGVSLYSYSGDLYTSMSLEDAMADIADIGATGIEILGEGNIPGYPHPDPAWTDTWHRLLDRYGLTPTNYGSWVDTAMWRDRDLTAEEGRAQLERDLRLAKLLGFTSIRPKFGVVTPELDPHPIWQPAVERVLDLATDLDIVICPEIHSPTPIKHPVTQAYLDFIDRTGSDHFKLLIDTGIFQTAPVDDGHEGFEGKKRPPFLEPLAVPMSDLADVLPHVHFIQAKFFEIDDRLTDLHIPWPEILTTLRAAGWQGWLSSEYEGRREPYRGRDQVRRQHALLRTLSHDAAPGGDLD

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_LN831790_5	5.1|4134927|15|NZ_LN831790|CRISPRCasFinder	4134927-4134941	15	NZ_LN831790.1	2117126-2117140	0	1.0
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_LN831790.1	4569565-4569591	1	0.963
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_LN831790.1	7722038-7722059	1	0.955
NZ_LN831790_11	11.2|5459754|19|NZ_LN831790|CRISPRCasFinder	5459754-5459772	19	NZ_LN831790.1	2315618-2315636	1	0.947
NZ_LN831790_7	7.1|4377025|50|NZ_LN831790|CRISPRCasFinder	4377025-4377074	50	NZ_LN831790.1	4377062-4377111	2	0.96
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_LN831790.1	2715184-2715205	2	0.909
NZ_LN831790_11	11.2|5459754|19|NZ_LN831790|CRISPRCasFinder	5459754-5459772	19	NZ_LN831790.1	41486-41504	2	0.895
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_LN831790.1	2269310-2269343	2	0.941
NZ_LN831790_15	15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7103012-7103047	36	NZ_LN831788.1	80416-80451	2	0.944

1. spacer 5.1|4134927|15|NZ_LN831790|CRISPRCasFinder matches to position: 2117126-2117140, mismatch: 0, identity: 1.0

ggaggcgggggcggc	CRISPR spacer
ggaggcgggggcggc	Protospacer
***************

2. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to position: 4569565-4569591, mismatch: 1, identity: 0.963

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgagaacgagatcgcccag	Protospacer
**********.****************

3. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to position: 7722038-7722059, mismatch: 1, identity: 0.955

cccgccgccgtcgaggacgccg	CRISPR spacer
cccgccgccgtcgtggacgccg	Protospacer
************* ********

4. spacer 11.2|5459754|19|NZ_LN831790|CRISPRCasFinder matches to position: 2315618-2315636, mismatch: 1, identity: 0.947

gctccggccgccgaggcag	CRISPR spacer
gctccggccgccgcggcag	Protospacer
************* *****

5. spacer 7.1|4377025|50|NZ_LN831790|CRISPRCasFinder matches to position: 4377062-4377111, mismatch: 2, identity: 0.96

tgtcccggcggcccccggagcgggtccggtggcccgctgtcccggcggcc	CRISPR spacer
tgtcccggcggcccccggagcgggtccggcggcccgccgtcccggcggcc	Protospacer
*****************************.*******.************

6. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to position: 2715184-2715205, mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
cccgccgccgtcgcggacggcg	Protospacer
************* ***** **

7. spacer 11.2|5459754|19|NZ_LN831790|CRISPRCasFinder matches to position: 41486-41504, mismatch: 2, identity: 0.895

gctccggccgccgaggcag	CRISPR spacer
gctccggccgccgggccag	Protospacer
*************.* ***

8. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to position: 2269310-2269343, mismatch: 2, identity: 0.941

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aagaccaccgccaagaaggccgcggccaagaaga	Protospacer
***** ************** *************

9. spacer 15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to position: 80416-80451, mismatch: 2, identity: 0.944

actccgcccgcggccgcgaaccgcaccgactccctc	CRISPR spacer
acgccgcccgccgccgcgaaccgcaccgactccctc	Protospacer
** ******** ************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_LR134455	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence	139596-139622	1	0.963
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NC_015314	Pseudonocardia dioxanivorans CB1190 plasmid pPSED01, complete sequence	180110-180131	1	0.955
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_AP012556	Mycobacterium avium subsp. hominissuis TH135 plasmid pMAH135, complete sequence	172663-172689	2	0.926
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	975568-975594	2	0.926
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_CP010410	Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence	79673-79699	2	0.926
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_LR134466	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 24, complete sequence	70770-70796	2	0.926
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP032324	Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence	521126-521147	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP021355	Rhodococcus sp. S2-17 plasmid pRB98, complete sequence	483852-483873	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	1548-1569	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	689682-689703	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	MT952845	Microbacterium phage GardenState, complete genome	7438-7459	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	MK880124	Microbacterium phage IAmGroot, complete genome	8082-8103	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_LR134445	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 3, complete sequence	26571-26592	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP039426	Citricoccus sp. SGAir0253 plasmid unnamed2, complete sequence	8522-8543	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	568475-568496	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NC_017957	Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence	159258-159279	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP016821	Rhodococcus sp. p52 plasmid pDF01, complete sequence	114463-114484	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP039431	Citricoccus sp. SGAir0453 plasmid unnamed2, complete sequence	8522-8543	2	0.909
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	MK814759	Gordonia phage Reyja, complete genome	4844-4865	2	0.909
NZ_LN831790_15	15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7103012-7103047	36	NZ_LN831788	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence	80416-80451	2	0.944
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	130832-130858	3	0.889
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	602205-602231	3	0.889
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MT771343	Gordonia phage Clown, complete genome	32730-32756	3	0.889
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4453500-4453526	3	0.889
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	536836-536857	3	0.864
NZ_LN831790_11	11.1|5459709|22|NZ_LN831790|CRISPRCasFinder	5459709-5459730	22	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	191366-191387	3	0.864
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_LR134452	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 10, complete sequence	86157-86184	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	CP000663	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence	255888-255915	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	253399-253426	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP018229	Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence	51915-51942	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MH271308	Microbacterium phage Percival, complete genome	6830-6857	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP022209	Burkholderia gladioli pv. gladioli strain FDAARGOS_188 plasmid unnamed1, complete sequence	159113-159140	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP009321	Burkholderia gladioli strain ATCC 10248 plasmid 1, complete sequence	177867-177894	4	0.857
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP022007	Burkholderia gladioli pv. gladioli strain KACC 11889 plasmid pls1, complete sequence	105233-105260	4	0.857
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP021356	Rhodococcus sp. S2-17 plasmid pRB29, complete sequence	15604-15634	4	0.871
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP026974	Achromobacter insolitus strain FDAARGOS_88 plasmid unnamed1, complete sequence	54114-54140	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP039641	Azospirillum sp. TSH100 plasmid p2, complete sequence	12292-12318	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MK882925	Dinoroseobacter phage vB_DshS-R4C, complete genome	7455-7481	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1010229-1010255	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1332654-1332680	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1827843-1827869	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	396777-396803	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	396789-396815	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	792671-792697	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032349	Azospirillum brasilense strain MTCC4039 plasmid p3, complete sequence	355687-355713	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1339717-1339743	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_010311	Streptomyces sp. HK1 plasmid pSHK1, complete sequence	167515-167541	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP020568	Kitasatospora aureofaciens strain DM-1 plasmid unnamed1, complete sequence	105750-105776	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	CP000385	Mycobacterium sp. MCS Plasmid1, complete sequence	121323-121349	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	26623-26649	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP013454	Burkholderia vietnamiensis strain MSMB608WGS plasmid pMSMB608, complete sequence	38033-38059	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_011962	Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence	141654-141680	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP029339	Streptomyces sp. SM17 plasmid pSM17A, complete sequence	14911-14937	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_008704	Mycobacterium sp. KMS plasmid pMKMS02, complete sequence	147382-147408	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	CP040467	Streptomyces albidoflavus strain UYFA156 plasmid unnamed, complete sequence	213830-213856	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MK937600	Mycobacterium phage Wigglewiggle, complete genome	23133-23159	4	0.852
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	KU997639	Mycobacterium phage Loadrie, complete genome	23133-23159	4	0.852
NZ_LN831790_12	12.2|5460057|25|NZ_LN831790|CRISPRCasFinder	5460057-5460081	25	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	73478-73502	4	0.84
NZ_LN831790_12	12.2|5460057|25|NZ_LN831790|CRISPRCasFinder	5460057-5460081	25	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	884111-884135	4	0.84
NZ_LN831790_12	12.2|5460057|25|NZ_LN831790|CRISPRCasFinder	5460057-5460081	25	NZ_CP011274	Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence	29124-29148	4	0.84
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_018452	Burkholderia phage DC1, complete genome	55672-55699	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	FJ937737	Burkholderia cenocepacia phage BcepIL02, complete genome	56494-56521	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_005262	Burkholderia cepacia phage Bcep22, complete genome	57536-57563	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_012743	Burkholderia phage BcepIL02, complete genome	56494-56521	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_021209	Sinorhizobium sp. M14 plasmid pSinA, complete sequence	61910-61937	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_KU140623	Sinorhizobium sp. M14 plasmid pSinB, complete sequence	248313-248340	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP044544	Bradyrhizobium betae strain PL7HG1 plasmid pBbPL7HG1, complete sequence	75074-75101	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MG757166	Gordonia phage SuperSulley, complete genome	23169-23196	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MH779499	Gordonia phage Buggaboo, complete genome	23169-23196	5	0.821
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	1168918-1168945	5	0.821
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	130820-130846	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP021814	Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence	1412281-1412307	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1820030-1820056	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP019460	Streptomyces autolyticus strain CGMCC0516 plasmid unnamed3, complete sequence	5667-5693	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP019460	Streptomyces autolyticus strain CGMCC0516 plasmid unnamed3, complete sequence	21151-21177	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP020695	Sulfitobacter sp. D7 plasmid p1SUD7, complete sequence	183862-183888	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	540467-540493	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1005622-1005648	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1229401-1229427	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_005241	Cupriavidus necator H16 megaplasmid pHG1, complete sequence	100338-100364	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1395457-1395483	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_019959	Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence	64717-64743	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP039289	Cupriavidus necator H16 plasmid pHG1, complete sequence	100338-100364	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	624922-624948	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	736918-736944	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032685	Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence	736871-736897	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP019438	Thioclava nitratireducens strain 25B10_4 plasmid unnamed1, complete sequence	57168-57194	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	144882-144908	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032828	Sphingomonas sp. YZ-8 plasmid unnamed1, complete sequence	701823-701849	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP018096	Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence	157997-158023	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032690	Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence	736420-736446	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	583081-583107	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	681964-681990	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	142686-142712	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP052758	Cellulosimicrobium sp. BI34T plasmid pCPRO01, complete sequence	4426-4452	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	20042-20068	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	138460-138486	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP011518	Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence	11148-11174	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP011518	Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence	451683-451709	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_023283	Streptomyces sp. FR1 plasmid pFRL3, complete sequence	181237-181263	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_023284	Streptomyces sp. F2 plasmid pFRL4, complete sequence	217865-217891	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_009939	Deinococcus geothermalis DSM 11300 plasmid pDGEO02, complete sequence	99372-99398	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP029359	Azospirillum sp. CFH 70021 plasmid unnamed4	7963-7989	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	703151-703177	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013857	Azospirillum sp. B510 plasmid pAB510c, complete sequence	619625-619651	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP039433	Rhodococcus sp. SGAir0479 plasmid unnamed	75777-75803	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	471283-471309	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP026489	Streptomyces sp. 604F plasmid unnamed, complete sequence	42406-42432	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	165623-165649	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	750790-750816	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_016586	Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence	316644-316670	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	KX641263	Mycobacterium phage Kalpine, complete genome	5955-5981	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	JN408461	Mycobacterium phage Trixie, complete genome	5823-5849	5	0.815
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MT889371	Microbacterium phage DelaGarza, complete genome	19894-19920	5	0.815
NZ_LN831790_10	10.2|5015249|27|NZ_LN831790|PILER-CR	5015249-5015275	27	NC_016972	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG2, complete sequence	57044-57070	5	0.815
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP044544	Bradyrhizobium betae strain PL7HG1 plasmid pBbPL7HG1, complete sequence	100711-100738	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP006370	Aureimonas sp. AU20 plasmid pAU20c, complete sequence	51642-51669	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP017077	Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence	103265-103292	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_017536	Oligotropha carboxidovorans OM4 plasmid pHCG3B, complete sequence	5247-5274	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	267025-267052	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP015032	Burkholderia cenocepacia strain 842 plasmid pBcn842-1, complete sequence	63739-63766	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_015689	Oligotropha carboxidovorans OM5 plasmid pHCG3, complete sequence	5248-5275	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_023286	Streptomyces sp. F12 plasmid pFRL6, complete sequence	247730-247757	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	346999-347026	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_019309	Pseudomonas sp. K-62 plasmid pMR68, complete sequence	456-483	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KU716095	Mycobacterium phage Myxus, complete genome	6924-6951	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK061409	Mycobacterium phage ExplosioNervosa, complete genome	6957-6984	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK016499	Mycobacterium phage Mangethe, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MG872842	Mycobacterium phage Scherzo, complete genome	6957-6984	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK919480	Mycobacterium phage Techage, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KX585252	Mycobacterium phage HortumSL17, complete genome	6924-6951	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MN369741	Mycobacterium phage LoneWolf, complete genome	6771-6798	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MN234172	Mycobacterium phage ThulaThula, complete genome	3675-3702	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KX641262	Mycobacterium phage Nazo, complete genome	3633-3660	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KT285706	Mycobacterium phage Pioneer, complete genome	6957-6984	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK977713	Mycobacterium phage Tubs, complete genome	6924-6951	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MN369763	Mycobacterium phage Aliter, complete genome	6852-6879	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MN234200	Mycobacterium phage Maminiaina, complete genome	6694-6721	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MF919492	Mycobacterium phage Arib1, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK524489	Mycobacterium phage Ugenie5, complete genome	6957-6984	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KX664447	Mycobacterium phage Phaeder, complete genome	6924-6951	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MN585978	Mycobacterium phage Beemo, complete genome	6958-6985	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_041969	Mycobacterium phage Jebeks, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_023552	Mycobacterium phage Donovan, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KU613353	Mycobacterium phage Catalina, complete genome	6925-6952	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MF472894	Mycobacterium phage Majeke, complete genome	3666-3693	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MK376962	Gordonia phage NosilaM, complete genome	22981-23008	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_023692	Mycobacterium phage BigNuz, complete genome	3633-3660	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KR080195	Mycobacterium phage Phayonce, complete genome	3630-3657	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	MG872840	Mycobacterium phage Phonnegut, complete genome	6957-6984	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_042314	Mycobacterium virus PackMan, complete genome	6924-6951	6	0.786
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	KX685355	Mycobacterium phage Qobbit, complete genome	6954-6981	6	0.786
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP040819	Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence	477624-477654	6	0.806
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_AP022849	Bosea sp. ANAM02 plasmid pANAM02, complete sequence	507605-507635	6	0.806
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1591946-1591972	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_003078	Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence	221954-221980	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP006990	Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence	192869-192895	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP024426	Paracoccus yeei strain TT13 plasmid pTT13-4, complete sequence	73885-73911	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP021799	Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence	289491-289517	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP009146	Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence	1469116-1469142	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP020445	Paracoccus yeei strain FDAARGOS_252 plasmid unnamed5, complete sequence	13695-13721	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013859	Azospirillum sp. B510 plasmid pAB510e, complete sequence	209011-209037	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013859	Azospirillum sp. B510 plasmid pAB510e, complete sequence	415385-415411	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	1283220-1283246	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP021802	Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence	101568-101594	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP021831	Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence	86337-86363	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP026527	Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence	1513236-1513262	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP044079	Paracoccus yeei strain FDAARGOS_643 plasmid unnamed2, complete sequence	27532-27558	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP031079	Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence	393821-393847	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	708588-708614	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NZ_CP026517	Deinococcus sp. NW-56 plasmid unnamed1, complete sequence	367158-367184	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	NC_020560	Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence	221954-221980	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MN693814	Marine virus AFVG_250M1086, complete genome	22476-22502	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MF668280	Mycobacterium phage Phabba, complete genome	43078-43104	6	0.778
NZ_LN831790_5	5.2|4134966|27|NZ_LN831790|CRISPRCasFinder	4134966-4134992	27	MH319743	Marine virus AG-345-E15 Ga0172270_13 genomic sequence	6287-6313	6	0.778
NZ_LN831790_10	10.4|5015243|37|NZ_LN831790|CRISPRCasFinder	5015243-5015279	37	NZ_LR134455	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence	139590-139626	6	0.838
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	125744-125777	6	0.824
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	KJ410133	Mycobacterium phage Jolie2, complete genome	99-132	6	0.824
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP017303	Rhodococcus sp. YL-1 plasmid pYLL1 sequence	169518-169552	6	0.829
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP034156	Rhodococcus sp. NJ-530 plasmid unnamed4, complete sequence	412367-412401	6	0.829
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	LR606148	Rhizobium sp. Q54 genome assembly, plasmid: 5	267272-267299	7	0.75
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP049244	Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence	1114367-1114394	7	0.75
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	349025-349052	7	0.75
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP042332	Bosea sp. F3-2 plasmid pB32-1, complete sequence	113669-113696	7	0.75
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NC_027348	Delftia phage RG-2014, complete genome	72995-73022	7	0.75
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP044080	Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence	117237-117267	7	0.774
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	KR604693	Pectobacterium phage Peat1, complete genome	10777-10807	7	0.774
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_AP022607	Mycobacterium branderi strain JCM 12687 plasmid pJCM12687	448501-448531	7	0.774
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP027023	Streptomyces sp. WAC00288 plasmid p1, complete sequence	184149-184179	7	0.774
NZ_LN831790_6	6.2|4180814|30|NZ_LN831790|CRISPRCasFinder	4180814-4180843	30	NZ_CP020556	Streptomyces sp. Sge12 plasmid pSGE, complete sequence	25651-25680	7	0.767
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_LR134460	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence	2332-2365	7	0.794
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	KT186229	Streptomyces phage Verse, complete genome	24785-24818	7	0.794
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MN428057	Gordonia phage Suerte, complete genome	8846-8879	7	0.794
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	KT186228	Streptomyces phage Amela, complete genome	24791-24824	7	0.794
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MN428048	Gordonia phage DobbysSock, complete genome	8846-8879	7	0.794
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MN693903	Marine virus AFVG_250M471, complete genome	39865-39898	7	0.794
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	52656-52690	7	0.8
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NC_016586	Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence	528353-528387	7	0.8
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP009439	Streptomyces glaucescens strain GLA.O plasmid pSglau1, complete sequence	13113-13147	7	0.8
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_LR134452	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 10, complete sequence	379577-379604	8	0.714
NZ_LN831790_2	2.2|2517291|28|NZ_LN831790|CRISPRCasFinder	2517291-2517318	28	NZ_CP013125	Pseudomonas mendocina S5.2 plasmid pPME5, complete sequence	188856-188883	8	0.714
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	NZ_CP032685	Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence	1371256-1371289	8	0.765
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	NZ_CP032690	Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence	1371234-1371267	8	0.765
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	NC_018696	Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence	342187-342220	8	0.765
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NC_006363	Nocardia farcinica IFM 10152 plasmid pNF2, complete sequence	63369-63399	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NC_023282	Streptomyces sp. FR1 plasmid pFRL2, complete sequence	74157-74187	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP040820	Paraoceanicella profunda strain D4M1 plasmid pD4M1B, complete sequence	167313-167343	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NC_010851	Streptomyces sp. FR1 plasmid pFRL1, complete sequence	9662-9692	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	780937-780967	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP015446	Streptomyces sp. S8 plasmid unnamed, complete sequence	8043-8073	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	721363-721393	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP006369	Aureimonas sp. AU20 plasmid pAU20b, complete sequence	240286-240316	8	0.742
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_LR594664	Variovorax sp. RA8 plasmid 3	389859-389889	8	0.742
NZ_LN831790_10	10.4|5015243|37|NZ_LN831790|CRISPRCasFinder	5015243-5015279	37	NZ_LR134466	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 24, complete sequence	70764-70800	8	0.784
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	1243555-1243588	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MK878901	Gordonia phage HannahD, complete genome	10153-10186	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MT522006	Gordonia phage BBQValindra, complete genome	10131-10164	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MN813694	Gordonia phage Opie, complete genome	10489-10522	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MH479915	Gordonia phage GEazy, complete genome	10153-10186	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	KX815338	Streptomyces phage Joe, complete genome	23709-23742	8	0.765
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	199356-199389	8	0.765
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_019849	Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence	105544-105578	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_017326	Sinorhizobium meliloti SM11 plasmid pSmeSM11d, complete sequence	105349-105383	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_017323	Sinorhizobium meliloti BL225C plasmid pSINMEB02, complete sequence	1340628-1340662	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP009146	Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence	105633-105667	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_018701	Sinorhizobium meliloti Rm41 plasmid pSYMB, complete sequence	105528-105562	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP019083	Paludisphaera borealis strain PX4 plasmid PALBO1, complete sequence	102876-102910	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021802	Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence	371619-371653	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021820	Sinorhizobium meliloti strain M162 plasmid psymB, complete sequence	443844-443878	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021831	Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence	350502-350536	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021814	Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence	1671668-1671702	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021810	Sinorhizobium meliloti strain Rm41 plasmid psymB, complete sequence	894322-894356	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021218	Sinorhizobium meliloti RU11/001 plasmid pSymB, complete sequence	258841-258875	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP026527	Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence	108249-108283	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_003078	Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence	1635573-1635607	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP019586	Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymB, complete sequence	1600736-1600770	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021799	Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence	19778-19812	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021828	Sinorhizobium meliloti strain KH35c plasmid psymB, complete sequence	1206243-1206277	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021823	Sinorhizobium meliloti strain KH46 plasmid psymB, complete sequence	1319879-1319913	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021795	Sinorhizobium meliloti strain USDA1157 plasmid psymB, complete sequence	864435-864469	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP021806	Sinorhizobium meliloti strain T073 plasmid psymB, complete sequence	916426-916460	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP019484	Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence	162935-162969	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP019487	Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence	1526668-1526702	8	0.771
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_020560	Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence	1635589-1635623	8	0.771
NZ_LN831790_16	16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112740-7112773	34	MT114166	Microbacterium phage Nike, complete genome	13927-13960	8	0.765
NZ_LN831790_16	16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112740-7112773	34	MN183284	Microbacterium phage Mashley, complete genome	13468-13501	8	0.765
NZ_LN831790_16	16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112740-7112773	34	NC_047973	Microbacterium phage Hyperion, complete genome	13657-13690	8	0.765
NZ_LN831790_16	16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112740-7112773	34	MT657333	Microbacterium phage Casend, complete genome	13842-13875	8	0.765
NZ_LN831790_16	16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112740-7112773	34	NC_047975	Microbacterium phage Squash, complete genome	13940-13973	8	0.765
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3335276-3335309	8	0.765
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_CP021409	Celeribacter manganoxidans strain DY25 plasmid pDY25-E, complete sequence	25474-25507	8	0.765
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	KC462197	Burkholderia phage ST79, complete genome	14654-14687	8	0.765
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	NZ_CP022370	Bosea sp. AS-1 plasmid unnamed1, complete sequence	159393-159426	9	0.735
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP030863	Streptomyces globosus strain LZH-48 plasmid unnamed1, complete sequence	100232-100262	9	0.71
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NC_009620	Sinorhizobium medicae WSM419 plasmid pSMED01, complete sequence	178353-178383	9	0.71
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NC_023283	Streptomyces sp. FR1 plasmid pFRL3, complete sequence	337930-337960	9	0.71
NZ_LN831790_3	3.1|2584149|31|NZ_LN831790|CRISPRCasFinder	2584149-2584179	31	NZ_CP020613	Paracoccus contaminans strain RKI 16-01929T=LMG 29738T=CCM 8701T=CIP 111112T plasmid unnamed, complete sequence	63497-63527	9	0.71
NZ_LN831790_10	10.4|5015243|37|NZ_LN831790|CRISPRCasFinder	5015243-5015279	37	NZ_CP010410	Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence	79669-79705	9	0.757
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MK061410	Gordonia phage Eyes, complete genome	10145-10178	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MK967377	Gordonia phage MagicMan, complete genome	10481-10514	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	KU998235	Gordonia phage Bowser, complete genome	10137-10170	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NC_031255	Gordonia phage Schwabeltier, complete genome	10482-10515	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050092	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence	225187-225220	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050081	Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence	93362-93395	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050098	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence	99952-99985	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050104	Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence	377999-378032	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP025013	Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence	101475-101508	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP049731	Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence	93767-93800	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP053440	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence	100591-100624	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP018229	Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence	866009-866042	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP025507	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence	78659-78692	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP016287	Rhizobium leguminosarum strain Vaf10 plasmid unnamed1, complete sequence	50955-50988	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050109	Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence	377999-378032	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP048281	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence	121440-121473	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP030761	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence	194606-194639	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP054022	Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence	281776-281809	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NC_012848	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence	729570-729603	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP022666	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence	805726-805759	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP054032	Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence	25235-25268	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP022565	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK01, complete sequence	586077-586110	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP053206	Rhizobium leguminosarum bv. trifolii TA1 plasmid pRltTA1D, complete sequence	91851-91884	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP041605	Streptomyces sp. S1D4-14 plasmid pS1D4-14.1, complete sequence	93053-93086	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP050086	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence	402856-402889	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	AY526908	Bordetella phage BMP-1, complete genome	32793-32826	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	AY526908	Bordetella phage BMP-1, complete genome	41047-41080	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NC_005357	Bordetella phage BPP-1, complete genome	32791-32824	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NC_005357	Bordetella phage BPP-1, complete genome	40877-40910	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	AY526909	Bordetella phage BIP-1, complete genome	32792-32825	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	AY526909	Bordetella phage BIP-1, complete genome	41022-41055	9	0.735
NZ_LN831790_15	15.3|7102791|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7102791-7102826	36	NC_012520	Rhodococcus opacus B4 plasmid pROB01, complete sequence	198332-198367	9	0.75
NZ_LN831790_15	15.9|7103230|34|NZ_LN831790|CRT	7103230-7103263	34	NC_019202	Pseudomonas aeruginosa plasmid pKLC102, complete sequence	102649-102682	9	0.735
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	832508-832542	9	0.743
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	292759-292793	9	0.743
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	238083-238117	9	0.743
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	HQ711985	Pseudomonas phage vB_PaeS_PMG1, complete genome	6642-6676	9	0.743
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_023316	Streptomyces sp. 14R-10 plasmid pZL1, complete sequence	50308-50342	9	0.743
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP038257	Microbacterium sediminis strain YLB-01 plasmid unnamed, complete sequence	38763-38797	9	0.743
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_LR134456	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence	142122-142155	9	0.735
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_CP013856	Pseudonocardia sp. HH130630-07 plasmid pLS2-2, complete sequence	107544-107577	9	0.735
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_CP010421	Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence	68915-68948	9	0.735
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	NZ_CP010410	Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence	86542-86575	10	0.706
NZ_LN831790_13	13.1|5460396|34|NZ_LN831790|CRISPRCasFinder	5460396-5460429	34	MT708548	Streptomyces phage Salutena, complete genome	20787-20820	10	0.706
NZ_LN831790_16	16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112304-7112338	35	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1726308-1726342	10	0.714
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP049317	Caballeronia sp. SBC2 plasmid pSBC2-1, complete sequence	442500-442534	10	0.714
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NZ_CP049157	Caballeronia sp. SBC1 plasmid pSBC1_1, complete sequence	1201908-1201942	10	0.714
NZ_LN831790_16	16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112595-7112629	35	NC_017805	Deinococcus gobiensis I-0 plasmid P1, complete sequence	398776-398810	10	0.714
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	1604167-1604200	10	0.706
NZ_LN831790_16	16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7112884-7112917	34	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	570207-570240	10	0.706
NZ_LN831790_15	15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT	7103012-7103047	36	NZ_CP046573	Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence	418823-418858	11	0.694
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	KC900378	Pseudomonas phage LKA5, complete genome	49681-49714	12	0.647
NZ_LN831790_2	2.3|2517342|34|NZ_LN831790|CRISPRCasFinder	2517342-2517375	34	MT118301	Pseudomonas phage Epa33, complete genome	48111-48144	12	0.647

1. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NZ_LR134455 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence) position: , mismatch: 1, identity: 0.963

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgagaacgagatcgcccag	Protospacer
**********.****************

2. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NC_015314 (Pseudonocardia dioxanivorans CB1190 plasmid pPSED01, complete sequence) position: , mismatch: 1, identity: 0.955

cccgccgccgtcgaggacgccg	CRISPR spacer
cgcgccgccgtcgaggacgccg	Protospacer
* ********************

3. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_AP012556 (Mycobacterium avium subsp. hominissuis TH135 plasmid pMAH135, complete sequence) position: , mismatch: 2, identity: 0.926

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcggaggcggcggcggaggc	Protospacer
**********.*** ************

4. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 2, identity: 0.926

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgaaaacgagatcgcccag	Protospacer
**********..***************

5. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NZ_CP010410 (Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.926

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgagaacgagatcgcgcag	Protospacer
**********.************ ***

6. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NZ_LR134466 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 24, complete sequence) position: , mismatch: 2, identity: 0.926

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgagaacgagatcgcgcag	Protospacer
**********.************ ***

7. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032324 (Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gtcgccgccgtcgaggacgccg	Protospacer
 .********************

8. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021355 (Rhodococcus sp. S2-17 plasmid pRB98, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
cccgccgccgtcgaggacgcgt	Protospacer
********************  

9. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gtcgccgccgtcgaggacgccg	Protospacer
 .********************

10. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gtcgccgccgtcgaggacgccg	Protospacer
 .********************

11. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to MT952845 (Microbacterium phage GardenState, complete genome) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
accgccgccgtcgaggacgcca	Protospacer
 ********************.

12. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to MK880124 (Microbacterium phage IAmGroot, complete genome) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
accgccgccgtcgaggacgcca	Protospacer
 ********************.

13. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134445 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 3, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gccgccgccgtcgacgacgccg	Protospacer
 ************* *******

14. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP039426 (Citricoccus sp. SGAir0253 plasmid unnamed2, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
accgccgccgtcgaggccgccg	Protospacer
 *************** *****

15. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gccgccgccgtcgaggccgccg	Protospacer
 *************** *****

16. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NC_017957 (Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gccgccgccgtcgaggccgccg	Protospacer
 *************** *****

17. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP016821 (Rhodococcus sp. p52 plasmid pDF01, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
gcctccgccgtcgaggacgccg	Protospacer
 ** ******************

18. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP039431 (Citricoccus sp. SGAir0453 plasmid unnamed2, complete sequence) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
accgccgccgtcgaggccgccg	Protospacer
 *************** *****

19. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to MK814759 (Gordonia phage Reyja, complete genome) position: , mismatch: 2, identity: 0.909

cccgccgccgtcgaggacgccg	CRISPR spacer
cccgccgccgtcgaggacgtca	Protospacer
*******************.*.

20. spacer 15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LN831788 (Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence) position: , mismatch: 2, identity: 0.944

actccgcccgcggccgcgaaccgcaccgactccctc	CRISPR spacer
acgccgcccgccgccgcgaaccgcaccgactccctc	Protospacer
** ******** ************************

21. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 3, identity: 0.889

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcggagggggcggcggaggg	Protospacer
** *******.*************** 

22. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 3, identity: 0.889

gggggcggcgaagggggcggcggaggc	CRISPR spacer
aggggcggcggagggggtggcggaggc	Protospacer
.*********.******.*********

23. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MT771343 (Gordonia phage Clown, complete genome) position: , mismatch: 3, identity: 0.889

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggatgcggcgaaggtggcggcggaggc	Protospacer
**. ********** ************

24. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 3, identity: 0.889

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
ccgcaccacgagaacgagatcgcgcaa	Protospacer
**********.************ **.

25. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 3, identity: 0.864

cccgccgccgtcgaggacgccg	CRISPR spacer
gtcgccgccgtcgaggacgcca	Protospacer
 .*******************.

26. spacer 11.1|5459709|22|NZ_LN831790|CRISPRCasFinder matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 3, identity: 0.864

cccgccgccgtcgaggacgccg	CRISPR spacer
gtcgccgccgtcgaggacgcca	Protospacer
 .*******************.

27. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134452 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 10, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gccgcctcggccggcttctcggcctcga	Protospacer
*  ****************** *****.

28. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to CP000663 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcctcggccgccttctcgccctcgg	Protospacer
*   ********* **************

29. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcctcggccgccttctcgccctcgg	Protospacer
*   ********* **************

30. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP018229 (Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gctgcctcggccggcttttcgcccgcgg	Protospacer
*  **************.****** ***

31. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MH271308 (Microbacterium phage Percival, complete genome) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcggactcggcgggcttctcgccctcgg	Protospacer
* .* ****** ****************

32. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022209 (Burkholderia gladioli pv. gladioli strain FDAARGOS_188 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gaagtgttggccggcttctcgccctcgg	Protospacer
*.**. *.********************

33. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP009321 (Burkholderia gladioli strain ATCC 10248 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gaagtgttggccggcttctcgccctcgg	Protospacer
*.**. *.********************

34. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022007 (Burkholderia gladioli pv. gladioli strain KACC 11889 plasmid pls1, complete sequence) position: , mismatch: 4, identity: 0.857

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gaagtgttggccggcttctcgccctcgg	Protospacer
*.**. *.********************

35. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021356 (Rhodococcus sp. S2-17 plasmid pRB29, complete sequence) position: , mismatch: 4, identity: 0.871

cgcg-cccgtggtcttcttcgccgccgcggcg	CRISPR spacer
-gcgccccgtgtgcttcttcgccgccgcggcc	Protospacer
 *** ******  ****************** 

36. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP026974 (Achromobacter insolitus strain FDAARGOS_88 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgatgggggcggcggaacg	Protospacer
*********** ************.  

37. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP039641 (Azospirillum sp. TSH100 plasmid p2, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cccggcggcgaaggcggcggcggaggc	Protospacer
   *********** ************

38. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MK882925 (Dinoroseobacter phage vB_DshS-R4C, complete genome) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaagggggcggcggggtg	Protospacer
** ********************.*  

39. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtcggcggcgaaggcggcgccggaggc	Protospacer
*  *********** **** *******

40. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtcggcggcgaaggcggcgccggaggc	Protospacer
*  *********** **** *******

41. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtcggcggcgaaggcggcgccggaggc	Protospacer
*  *********** **** *******

42. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgacgggggcggcgacggg	Protospacer
*********** **********. ** 

43. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgacgggggcggcgacggg	Protospacer
*********** **********. ** 

44. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtcggcggcgaaggcggcgccggaggc	Protospacer
*  *********** **** *******

45. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032349 (Azospirillum brasilense strain MTCC4039 plasmid p3, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtagccggcggagggggcggcggaggc	Protospacer
* .* *****.****************

46. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtcggcggcgaaggcggcgccggaggc	Protospacer
*  *********** **** *******

47. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_010311 (Streptomyces sp. HK1 plasmid pSHK1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagcggggggcggggcc	Protospacer
************* *** *****.* *

48. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP020568 (Kitasatospora aureofaciens strain DM-1 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaagcgggcggcgggagc	Protospacer
** ********** *********..**

49. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to CP000385 (Mycobacterium sp. MCS Plasmid1, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggggtcggcggccgc	Protospacer
** ************* ******  **

50. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggatgcggccaagggggcggcggagac	Protospacer
**. ***** ***************.*

51. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP013454 (Burkholderia vietnamiensis strain MSMB608WGS plasmid pMSMB608, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gagcgcggcgaagggggcggcgtcggc	Protospacer
*.* ******************  ***

52. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_011962 (Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gagcgcggcgaaggcggcggcggcggc	Protospacer
*.* ********** ******** ***

53. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP029339 (Streptomyces sp. SM17 plasmid pSM17A, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagcggggggcggggcc	Protospacer
************* *** *****.* *

54. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_008704 (Mycobacterium sp. KMS plasmid pMKMS02, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggggtcggcggccgc	Protospacer
** ************* ******  **

55. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to CP040467 (Streptomyces albidoflavus strain UYFA156 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgccgggggcggcggtgac	Protospacer
**********  *********** *.*

56. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MK937600 (Mycobacterium phage Wigglewiggle, complete genome) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggtggcggcgaaggtggcggcggtgcc	Protospacer
** *********** ******** * *

57. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to KU997639 (Mycobacterium phage Loadrie, complete genome) position: , mismatch: 4, identity: 0.852

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggtggcggcgaaggtggcggcggtgcc	Protospacer
** *********** ******** * *

58. spacer 12.2|5460057|25|NZ_LN831790|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 4, identity: 0.84

gtggtcctcccggccgccaccgagc	CRISPR spacer
gtggtcgtcccggccgccgccgaca	Protospacer
****** ***********.****  

59. spacer 12.2|5460057|25|NZ_LN831790|CRISPRCasFinder matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 4, identity: 0.84

gtggtcctcccggccgccaccgagc	CRISPR spacer
caggtcctctcggccgccagcgagc	Protospacer
  *******.********* *****

60. spacer 12.2|5460057|25|NZ_LN831790|CRISPRCasFinder matches to NZ_CP011274 (Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence) position: , mismatch: 4, identity: 0.84

gtggtcctcccggccgccaccgagc	CRISPR spacer
cgggtcttctcggccgccaccgagc	Protospacer
  ****.**.***************

61. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_018452 (Burkholderia phage DC1, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcgtcggccggcttctcgccctcga	Protospacer
*   * *********************.

62. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to FJ937737 (Burkholderia cenocepacia phage BcepIL02, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcgtcggccggcttctcgccctcga	Protospacer
*   * *********************.

63. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_005262 (Burkholderia cepacia phage Bcep22, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcgtcggccggcttctcgccctcga	Protospacer
*   * *********************.

64. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_012743 (Burkholderia phage BcepIL02, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcctcgtcggccggcttctcgccctcga	Protospacer
*   * *********************.

65. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_021209 (Sinorhizobium sp. M14 plasmid pSinA, complete sequence) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gccggctcggccggcttctcggcctcga	Protospacer
*  * **************** *****.

66. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_KU140623 (Sinorhizobium sp. M14 plasmid pSinB, complete sequence) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gccggctcggccggcttctcggcctcga	Protospacer
*  * **************** *****.

67. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP044544 (Bradyrhizobium betae strain PL7HG1 plasmid pBbPL7HG1, complete sequence) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gccggctcggccggcttctcggcctcga	Protospacer
*  * **************** *****.

68. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MG757166 (Gordonia phage SuperSulley, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcgtcctcggcaggcttctcggcctcgg	Protospacer
* . ******* ********* ******

69. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MH779499 (Gordonia phage Buggaboo, complete genome) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcgtcctcggcaggcttctcggcctcgg	Protospacer
* . ******* ********* ******

70. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 5, identity: 0.821

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
aggggctcggccggcatctcgccgtcgg	Protospacer
.*.* ********** ******* ****

71. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcggagggggcggaggtgct	Protospacer
**********.********* ** * .

72. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021814 (Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagggggcggcaatctc	Protospacer
*********************..   *

73. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtgggcggcgaagggggcggccgggcg	Protospacer
* ******************* *.*  

74. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP019460 (Streptomyces autolyticus strain CGMCC0516 plasmid unnamed3, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcggagggggcggggggcgg	Protospacer
**********.********* **. * 

75. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP019460 (Streptomyces autolyticus strain CGMCC0516 plasmid unnamed3, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcggagggggcggggggcgg	Protospacer
**********.********* **. * 

76. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP020695 (Sulfitobacter sp. D7 plasmid p1SUD7, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
aacggcggccaagggggcggcggagcc	Protospacer
.. ****** *************** *

77. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gcaggcggcgaaggaggaggcggagga	Protospacer
* .***********.** ******** 

78. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggccaagggggctgcggtctc	Protospacer
********* ******** ****   *

79. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtgggcggcgaagggggcggccgggcg	Protospacer
* ******************* *.*  

80. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_005241 (Cupriavidus necator H16 megaplasmid pHG1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcggagggggcggcggatcg	Protospacer
** *******.*************   

81. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gcaggcggcgaaggaggaggcggagga	Protospacer
* .***********.** ******** 

82. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_019959 (Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgacgggggcggcggaccg	Protospacer
** ******** ************   

83. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP039289 (Cupriavidus necator H16 plasmid pHG1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcggagggggcggcggatcg	Protospacer
** *******.*************   

84. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgcggggggcggcggaacg	Protospacer
********** .************.  

85. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gcaggcggcgaaggaggaggcggagga	Protospacer
* .***********.** ******** 

86. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032685 (Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
atggccggcgaagggggcggcggcgtc	Protospacer
. ** ****************** * *

87. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP019438 (Thioclava nitratireducens strain 25B10_4 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gctgcgggcgaaaggggcggcggaggc	Protospacer
*  *  ******.**************

88. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggaggcggcggcgag	Protospacer
** ***********.******** *. 

89. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032828 (Sphingomonas sp. YZ-8 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcggagggggcggcggcctc	Protospacer
** *******.************   *

90. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP018096 (Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cgccgcggcgaaggcggcggtggaggc	Protospacer
 *  ********** *****.******

91. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032690 (Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
atggccggcgaagggggcggcggcgtc	Protospacer
. ** ****************** * *

92. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cggggcggcggacggggcggcggacgg	Protospacer
 *********.* *********** * 

93. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
aggggtggcgacgggggcggcggacgg	Protospacer
.****.***** ************ * 

94. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cggggcggcgacgggggcggcgtccgc	Protospacer
 ********** **********   **

95. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP052758 (Cellulosimicrobium sp. BI34T plasmid pCPRO01, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggcgcggcgacgggggcggcggcgaa	Protospacer
*** ******* *********** *. 

96. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggaggcggcggcgag	Protospacer
** ***********.******** *. 

97. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
aggggtggcgacgggggcggcggacgg	Protospacer
.****.***** ************ * 

98. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP011518 (Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cggggcggcgcacggggcggcggaaga	Protospacer
 ********* * ***********.* 

99. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP011518 (Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagggggcgaagccgcc	Protospacer
*******************. *  * *

100. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_023283 (Streptomyces sp. FR1 plasmid pFRL3, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgatggcggcggcggagtc	Protospacer
 .********* ** ********** *

101. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_023284 (Streptomyces sp. F2 plasmid pFRL4, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgatggcggcggcggagtc	Protospacer
 .********* ** ********** *

102. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_009939 (Deinococcus geothermalis DSM 11300 plasmid pDGEO02, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaacagggcggcggcgag	Protospacer
************ .********* *. 

103. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP029359 (Azospirillum sp. CFH 70021 plasmid unnamed4) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gcgggcggagaagggggaggcggagaa	Protospacer
* ****** ******** *******. 

104. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggggacgggggcggcggctgg	Protospacer
******** ** ***********  * 

105. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013857 (Azospirillum sp. B510 plasmid pAB510c, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gagggcggcgaaggcggcggcggcacc	Protospacer
*.************ ******** . *

106. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP039433 (Rhodococcus sp. SGAir0479 plasmid unnamed) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggtgaaggtggcggcggccgt	Protospacer
********.***** ********  *.

107. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cgaggcggcgaagggggtggcggtgga	Protospacer
 *.**************.***** ** 

108. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP026489 (Streptomyces sp. 604F plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtaggcggcgaggtgggcggcggaggg	Protospacer
* .********.* ************ 

109. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gaaggcggcgaaggggacggcgaaggg	Protospacer
*..*************.*****.*** 

110. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggaggcggcggcgag	Protospacer
** ***********.******** *. 

111. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_016586 (Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcggcgggggcggcggtccc	Protospacer
**********. ***********   *

112. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to KX641263 (Mycobacterium phage Kalpine, complete genome) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggcggcggcggtgcg	Protospacer
** *********** ******** *  

113. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to JN408461 (Mycobacterium phage Trixie, complete genome) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggcggcggcggtgtg	Protospacer
** *********** ******** *  

114. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MT889371 (Microbacterium phage DelaGarza, complete genome) position: , mismatch: 5, identity: 0.815

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gtacgcggcgaaggtggcggcggcggc	Protospacer
* . ********** ******** ***

115. spacer 10.2|5015249|27|NZ_LN831790|PILER-CR matches to NC_016972 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG2, complete sequence) position: , mismatch: 5, identity: 0.815

ccgcaccacgggaacgagatcgcccag	CRISPR spacer
gcgcaccacgggcacgagatccccgcg	Protospacer
 *********** ******** **  *

116. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP044544 (Bradyrhizobium betae strain PL7HG1 plasmid pBbPL7HG1, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gccggctcggccggcttctcggcctcca	Protospacer
*  * **************** **** .

117. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP006370 (Aureimonas sp. AU20 plasmid pAU20c, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
tccgcctcgtccggctcctcgccctcgc	Protospacer
   ****** ******.********** 

118. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP017077 (Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
agttcctcggcctgcttctcgcccacgc	Protospacer
.*  ******** *********** ** 

119. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_017536 (Oligotropha carboxidovorans OM4 plasmid pHCG3B, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
ggcgcctcggccggcttctctccggtcg	Protospacer
** ***************** **  . *

120. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtgtcctcggccgggttctcgctctcga	Protospacer
* . ********** *******.****.

121. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP015032 (Burkholderia cenocepacia strain 842 plasmid pBcn842-1, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
aacgtctcggcccgcttctcgcgctcgg	Protospacer
.. *.******* ********* *****

122. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_015689 (Oligotropha carboxidovorans OM5 plasmid pHCG3, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
ggcgcctcggccggcttctctccggtcg	Protospacer
** ***************** **  . *

123. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_023286 (Streptomyces sp. F12 plasmid pFRL6, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
agcgccttggccggctgctcgccctctt	Protospacer
.* ****.******** *********  

124. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtgtcctcggccgtcttcttgccctcgc	Protospacer
* . ********* *****.******* 

125. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_019309 (Pseudomonas sp. K-62 plasmid pMR68, complete sequence) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gctgccgcggccggcttctcgcccgtgt	Protospacer
*  *** ***************** .* 

126. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KU716095 (Mycobacterium phage Myxus, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

127. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK061409 (Mycobacterium phage ExplosioNervosa, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

128. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK016499 (Mycobacterium phage Mangethe, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

129. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MG872842 (Mycobacterium phage Scherzo, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

130. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK919480 (Mycobacterium phage Techage, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

131. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KX585252 (Mycobacterium phage HortumSL17, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

132. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MN369741 (Mycobacterium phage LoneWolf, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

133. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MN234172 (Mycobacterium phage ThulaThula, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

134. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KX641262 (Mycobacterium phage Nazo, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

135. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KT285706 (Mycobacterium phage Pioneer, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

136. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK977713 (Mycobacterium phage Tubs, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

137. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MN369763 (Mycobacterium phage Aliter, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

138. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MN234200 (Mycobacterium phage Maminiaina, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

139. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MF919492 (Mycobacterium phage Arib1, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

140. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK524489 (Mycobacterium phage Ugenie5, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

141. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KX664447 (Mycobacterium phage Phaeder, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

142. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MN585978 (Mycobacterium phage Beemo, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

143. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_041969 (Mycobacterium phage Jebeks, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

144. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_023552 (Mycobacterium phage Donovan, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

145. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KU613353 (Mycobacterium phage Catalina, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

146. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MF472894 (Mycobacterium phage Majeke, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

147. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MK376962 (Gordonia phage NosilaM, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gcgtcctcggcgggcttctcggcctcgc	Protospacer
* . ******* ********* ***** 

148. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_023692 (Mycobacterium phage BigNuz, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

149. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KR080195 (Mycobacterium phage Phayonce, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cacggctcggcgggcttgtcgccctcgg	Protospacer
 . * ****** ***** **********

150. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to MG872840 (Mycobacterium phage Phonnegut, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

151. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_042314 (Mycobacterium virus PackMan, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

152. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to KX685355 (Mycobacterium phage Qobbit, complete genome) position: , mismatch: 6, identity: 0.786

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
gtcgcctcggccagcttcgcgccctccc	Protospacer
*  *********.***** *******  

153. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP040819 (Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence) position: , mismatch: 6, identity: 0.806

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggccgccgtggtcttcttcgccgcggcgggc	Protospacer
 **  ******************* ****  

154. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_AP022849 (Bosea sp. ANAM02 plasmid pANAM02, complete sequence) position: , mismatch: 6, identity: 0.806

cgcg-cccgtggtcttcttcgccgccgcggcg	CRISPR spacer
-gcgaaccgcggtcttcttcgccgcggcgaca	Protospacer
 ***  ***.*************** ***.*.

155. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ccaggcggcgcaggggacggcggaggt	Protospacer
  .******* *****.*********.

156. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_003078 (Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

157. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP006990 (Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagcgcggcgaaggcggcggcggagaa	Protospacer
 .* ********** **********. 

158. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP024426 (Paracoccus yeei strain TT13 plasmid pTT13-4, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgaaggcggcggcggtgaa	Protospacer
 .************ ******** *. 

159. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021799 (Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

160. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP009146 (Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

161. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP020445 (Paracoccus yeei strain FDAARGOS_252 plasmid unnamed5, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgaaggcggcggcggtgaa	Protospacer
 .************ ******** *. 

162. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013859 (Azospirillum sp. B510 plasmid pAB510e, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
accggcgccgcagggggcggcggaggg	Protospacer
.  **** ** *************** 

163. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013859 (Azospirillum sp. B510 plasmid pAB510e, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ggcggcggcgaaggcggcggcggcaag	Protospacer
** *********** ******** .. 

164. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
ctcggcggcgaagggggccgcggtggt	Protospacer
   *************** **** **.

165. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021802 (Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

166. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP021831 (Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

167. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP026527 (Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

168. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP044079 (Paracoccus yeei strain FDAARGOS_643 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgaaggcggcggcggtgaa	Protospacer
 .************ ******** *. 

169. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP031079 (Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgaaggcggcggcggtgaa	Protospacer
 .************ ******** *. 

170. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
actggcggcgaagcgcgcggcggagga	Protospacer
.  ********** * ********** 

171. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NZ_CP026517 (Deinococcus sp. NW-56 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cctggcggcgacgggggcgggggaggg	Protospacer
   ******** ******** ***** 

172. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to NC_020560 (Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
gggggcggcgaagagggcggcaatctc	Protospacer
*************.*******..   *

173. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MN693814 (Marine virus AFVG_250M1086, complete genome) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
tacggcggcgcagggggtggcggaggt	Protospacer
 . ******* ******.********.

174. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MF668280 (Mycobacterium phage Phabba, complete genome) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
cagggcggcgaagagggcggcgaagag	Protospacer
 .***********.********.**. 

175. spacer 5.2|4134966|27|NZ_LN831790|CRISPRCasFinder matches to MH319743 (Marine virus AG-345-E15 Ga0172270_13 genomic sequence) position: , mismatch: 6, identity: 0.778

gggggcggcgaagggggcggcggaggc	CRISPR spacer
tctggcggcggaggtggcggcggagga	Protospacer
   *******.*** *********** 

176. spacer 10.4|5015243|37|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134455 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence) position: , mismatch: 6, identity: 0.838

cgtgccgcaccacgggaacgagatcgcccaggccggg	CRISPR spacer
cttcccgcaccacgagaacgagatcgcccaggcccac	Protospacer
* * **********.******************* . 

177. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.824

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
accgcgatcgccaagaaggcggcggccgagaagg	Protospacer
*  .***.*******************.*****.

178. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to KJ410133 (Mycobacterium phage Jolie2, complete genome) position: , mismatch: 6, identity: 0.824

---aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cccaagccg---gccaagaaggcggcgcccaagaagc	Protospacer
   *** **   *************** ******** 

179. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017303 (Rhodococcus sp. YL-1 plasmid pYLL1 sequence) position: , mismatch: 6, identity: 0.829

aacgacgagacgctgcgcaaggcggccgagctcgc-	CRISPR spacer
gaggacgaggcgctgcgcaaggcggtcga-cgcgcg	Protospacer
.* ******.***************.*** * *** 

180. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP034156 (Rhodococcus sp. NJ-530 plasmid unnamed4, complete sequence) position: , mismatch: 6, identity: 0.829

aacgacgagacgctgcgcaaggcggccgagctcgc-	CRISPR spacer
gaggacgaggcgctgcgcaaggcggtcga-cgcgcg	Protospacer
.* ******.***************.*** * *** 

181. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to LR606148 (Rhizobium sp. Q54 genome assembly, plasmid: 5) position: , mismatch: 7, identity: 0.75

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
atcttgccggccggcttctcgccctcgg	Protospacer
.   . .*********************

182. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP049244 (Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.75

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cgagcctcgtgcggcttctcgccccaca	Protospacer
 ********  *************.  .

183. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 7, identity: 0.75

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
cgggcctcggccggcttctcccccagca	Protospacer
 *.***************** ***   .

184. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP042332 (Bosea sp. F3-2 plasmid pB32-1, complete sequence) position: , mismatch: 7, identity: 0.75

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
actaactgggccggcttctcgcgctcgg	Protospacer
.  . ** ************** *****

185. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NC_027348 (Delftia phage RG-2014, complete genome) position: , mismatch: 7, identity: 0.75

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
ttcttctcggcccacttctcgccctcgg	Protospacer
    .******* .**************

186. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP044080 (Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.774

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggtcgtcgtgggcttcttcgccgccgccgcg	Protospacer
 *.  .***** *************** ***

187. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to KR604693 (Pectobacterium phage Peat1, complete genome) position: , mismatch: 7, identity: 0.774

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
catgcccttggtcttcttcgccgccccatct	Protospacer
*..**** ***************** *. * 

188. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_AP022607 (Mycobacterium branderi strain JCM 12687 plasmid pJCM12687) position: , mismatch: 7, identity: 0.774

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
cgcatttctggtctgcttcgccgccgcggcc	Protospacer
***.... ****** *************** 

189. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP027023 (Streptomyces sp. WAC00288 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.774

cgcgcccgtggtcttcttcgccg----ccgcggcg	CRISPR spacer
cgcgcccgtggtcgtcgtcgccggcaaccac----	Protospacer
************* ** ******    **.*    

190. spacer 6.2|4180814|30|NZ_LN831790|CRISPRCasFinder matches to NZ_CP020556 (Streptomyces sp. Sge12 plasmid pSGE, complete sequence) position: , mismatch: 7, identity: 0.767

gggcgtacggccccgaggcggcgtacagct	CRISPR spacer
agctcgacggccccgaggcggcggacacct	Protospacer
.* .  ***************** *** **

191. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134460 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
gccgcgcccgccaagaaggcggcggcgaagaagg	Protospacer
.  .** ******************* ******.

192. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to KT186229 (Streptomyces phage Verse, complete genome) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aacgcaccggccaagaagacggcggcgaagaaga	Protospacer
** .*. * *********.******* *******

193. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MN428057 (Gordonia phage Suerte, complete genome) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aaccgggcagccaagaaggcggcccccaagaaga	Protospacer
**   *.* **************  *********

194. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to KT186228 (Streptomyces phage Amela, complete genome) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aacgcaccggccaagaagacggcggcgaagaaga	Protospacer
** .*. * *********.******* *******

195. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MN428048 (Gordonia phage DobbysSock, complete genome) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aaacgggcagccaagaaggcggcccccaagaaga	Protospacer
**.  *.* **************  *********

196. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MN693903 (Marine virus AFVG_250M471, complete genome) position: , mismatch: 7, identity: 0.794

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aaggctgctcccaagaaggcggctcccaagaaga	Protospacer
***.* .*. *************  *********

197. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.8

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggccggcca	Protospacer
 *  *** **************.**********..

198. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_016586 (Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence) position: , mismatch: 7, identity: 0.8

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggccggcca	Protospacer
 *  *** **************.**********..

199. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009439 (Streptomyces glaucescens strain GLA.O plasmid pSglau1, complete sequence) position: , mismatch: 7, identity: 0.8

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
agcgacgagacgctgcgcgaggcgtccaggatcac	Protospacer
*.****************.***** **..* **.*

200. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134452 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 10, complete sequence) position: , mismatch: 8, identity: 0.714

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
ttcgcctcggcgggcttctcgcccggct	Protospacer
   ******** ************    

201. spacer 2.2|2517291|28|NZ_LN831790|CRISPRCasFinder matches to NZ_CP013125 (Pseudomonas mendocina S5.2 plasmid pPME5, complete sequence) position: , mismatch: 8, identity: 0.714

ggagcctcggccggcttctcgccctcgg	CRISPR spacer
aacgcctcggccggcatctcgccccact	Protospacer
.. ************ ********.   

202. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032685 (Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence) position: , mismatch: 8, identity: 0.765

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
aattgctcgcgctcgagccggtcgcgctcctcct	Protospacer
  .* ***** ******* ***********. **

203. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP032690 (Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence) position: , mismatch: 8, identity: 0.765

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
aattgctcgcgctcgagccggtcgcgctcctcct	Protospacer
  .* ***** ******* ***********. **

204. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to NC_018696 (Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence) position: , mismatch: 8, identity: 0.765

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
ttgatatcgccttcgagcagctcgcgctccgcgt	Protospacer
**  * *****.******** *********   *

205. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NC_006363 (Nocardia farcinica IFM 10152 plasmid pNF2, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ttcggggcgggtcatcttcgccgccgcggcg	Protospacer
. **     **** *****************

206. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NC_023282 (Streptomyces sp. FR1 plasmid pFRL2, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggccgccgtggtcttcttcgccaccgccttc	Protospacer
 **  *****************.****  . 

207. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP040820 (Paraoceanicella profunda strain D4M1 plasmid pD4M1B, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ttcatgggtggccttcttcgcccccgcggcg	Protospacer
. *..  ****.********** ********

208. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NC_010851 (Streptomyces sp. FR1 plasmid pFRL1, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
cgacgccgtggtcttcttcgccaccgccttc	Protospacer
**   *****************.****  . 

209. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
gcagacggtgttcttcttcgccgccgcggtc	Protospacer
   * * *** ******************. 

210. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP015446 (Streptomyces sp. S8 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggccgccgtggtcttcttcgccaccgccttc	Protospacer
 **  *****************.****  . 

211. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
gcagacggtgttcttcttcgccgccgcggtc	Protospacer
   * * *** ******************. 

212. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP006369 (Aureimonas sp. AU20 plasmid pAU20b, complete sequence) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
cccctggctggtcttcttccccggcgcggcg	Protospacer
* * .   *********** *** *******

213. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_LR594664 (Variovorax sp. RA8 plasmid 3) position: , mismatch: 8, identity: 0.742

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
cgttgggttggtctgcttcgccgtcgcggcg	Protospacer
**.     ****** ********.*******

214. spacer 10.4|5015243|37|NZ_LN831790|CRISPRCasFinder matches to NZ_LR134466 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 24, complete sequence) position: , mismatch: 8, identity: 0.784

cgtgccgcaccacgggaacgagatcgcccaggccggg	CRISPR spacer
cttcccgcaccacgagaacgagatcgcgcaggcgcac	Protospacer
* * **********.************ *****  . 

215. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
aagcgcgcggccacgaaggcgccggccaagaagg	Protospacer
***   .* **** ******* ***********.

216. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MK878901 (Gordonia phage HannahD, complete genome) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgggcagccaccaagaaggcgccggccaagaagg	Protospacer
 .*.*..**.*********** ***********.

217. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MT522006 (Gordonia phage BBQValindra, complete genome) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgggcagccaccaagaaggcgccggccaagaagg	Protospacer
 .*.*..**.*********** ***********.

218. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MN813694 (Gordonia phage Opie, complete genome) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgggctgctgccaagaaggcgccggccaagaagg	Protospacer
 .*.* .*.************ ***********.

219. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MH479915 (Gordonia phage GEazy, complete genome) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgggcagccaccaagaaggcgccggccaagaagg	Protospacer
 .*.*..**.*********** ***********.

220. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to KX815338 (Streptomyces phage Joe, complete genome) position: , mismatch: 8, identity: 0.765

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
ccggcaccggccaagaaggcagcggcgaagaaga	Protospacer
  *.*. * ***********.***** *******

221. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 8, identity: 0.765

-aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
ctcgac-accgccaaggcggcggcggccaaggggg	Protospacer
   *** *********. *************..*.

222. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_019849 (Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

223. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_017326 (Sinorhizobium meliloti SM11 plasmid pSmeSM11d, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

224. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_017323 (Sinorhizobium meliloti BL225C plasmid pSINMEB02, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

225. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009146 (Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

226. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_018701 (Sinorhizobium meliloti Rm41 plasmid pSYMB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

227. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019083 (Paludisphaera borealis strain PX4 plasmid PALBO1, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggccgagctcgc---	CRISPR spacer
gacgaggagacgcttcgcaaggcggc---gttcgacga	Protospacer
.**** ******** ***********   *.***    

228. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021802 (Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

229. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021820 (Sinorhizobium meliloti strain M162 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

230. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021831 (Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

231. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021814 (Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

232. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021810 (Sinorhizobium meliloti strain Rm41 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

233. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021218 (Sinorhizobium meliloti RU11/001 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

234. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026527 (Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

235. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_003078 (Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

236. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019586 (Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

237. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021799 (Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

238. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021828 (Sinorhizobium meliloti strain KH35c plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

239. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021823 (Sinorhizobium meliloti strain KH46 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

240. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021795 (Sinorhizobium meliloti strain USDA1157 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

241. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021806 (Sinorhizobium meliloti strain T073 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

242. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019484 (Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

243. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019487 (Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

244. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_020560 (Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.771

aacgacgagacgctgcgcaaggcggc---cgagctcgc	CRISPR spacer
cacgacgagacgctgcccaaggaggcgcacaaggt---	Protospacer
 *************** ***** ***   *.** *   

245. spacer 16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to MT114166 (Microbacterium phage Nike, complete genome) position: , mismatch: 8, identity: 0.765

atgtggctggacacggacggctcccagctggcgg	CRISPR spacer
gtctgcgtcaacaccgacggcttccagctggcgg	Protospacer
.* **  * .**** *******.***********

246. spacer 16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to MN183284 (Microbacterium phage Mashley, complete genome) position: , mismatch: 8, identity: 0.765

atgtggctggacacggacggctcccagctggcgg	CRISPR spacer
gtctgcgtcaacaccgacggcttccagctggcgg	Protospacer
.* **  * .**** *******.***********

247. spacer 16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_047973 (Microbacterium phage Hyperion, complete genome) position: , mismatch: 8, identity: 0.765

atgtggctggacacggacggctcccagctggcgg	CRISPR spacer
gtctgcgtcaacaccgacggcttccagctggcgg	Protospacer
.* **  * .**** *******.***********

248. spacer 16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to MT657333 (Microbacterium phage Casend, complete genome) position: , mismatch: 8, identity: 0.765

atgtggctggacacggacggctcccagctggcgg	CRISPR spacer
gtctgcgtcaacaccgacggcttccagctggcgg	Protospacer
.* **  * .**** *******.***********

249. spacer 16.8|7112740|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_047975 (Microbacterium phage Squash, complete genome) position: , mismatch: 8, identity: 0.765

atgtggctggacacggacggctcccagctggcgg	CRISPR spacer
gtctgcgtcaacaccgacggcttccagctggcgg	Protospacer
.* **  * .**** *******.***********

250. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.765

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
tccacggcgggcaccatcgccgagatcgtcaccg	Protospacer
  *.   ********.******.***********

251. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021409 (Celeribacter manganoxidans strain DY25 plasmid pDY25-E, complete sequence) position: , mismatch: 8, identity: 0.765

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
gtcgtgatcggcgccgtcgccgggatcgtcatcg	Protospacer
* **   . ***.******************.**

252. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to KC462197 (Burkholderia phage ST79, complete genome) position: , mismatch: 8, identity: 0.765

gacgactcgggcaccgtcgccgggatcgtcaccg-	CRISPR spacer
aacccctcggccaccgtcgccgggagcgt-gcggt	Protospacer
.**  ***** ************** *** .* * 

253. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022370 (Bosea sp. AS-1 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
ttcgtctcgccctcgaggaggtcgctggtgcgcg	Protospacer
*** ************* *******   . *.* 

254. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP030863 (Streptomyces globosus strain LZH-48 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.71

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggacgccgtggtcttcttcgccaccgccttc	Protospacer
 *   *****************.****  . 

255. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NC_009620 (Sinorhizobium medicae WSM419 plasmid pSMED01, complete sequence) position: , mismatch: 9, identity: 0.71

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
gacgcccgtggtcttctgcgccgcgagcttg	Protospacer
 .*************** ****** .   .*

256. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NC_023283 (Streptomyces sp. FR1 plasmid pFRL3, complete sequence) position: , mismatch: 9, identity: 0.71

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
gggagagatggtcttcttcgcctacgcggcg	Protospacer
 * .   .**************  *******

257. spacer 3.1|2584149|31|NZ_LN831790|CRISPRCasFinder matches to NZ_CP020613 (Paracoccus contaminans strain RKI 16-01929T=LMG 29738T=CCM 8701T=CIP 111112T plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.71

cgcgcccgtggtcttcttcgccgccgcggcg	CRISPR spacer
ggtcgtggtggccttcttcgccgccgccgcc	Protospacer
 *.  . ****.*************** ** 

258. spacer 10.4|5015243|37|NZ_LN831790|CRISPRCasFinder matches to NZ_CP010410 (Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.757

cgtgccgcaccacgggaacgagatcgcccaggccggg	CRISPR spacer
gttcccgcaccacgagaacgagatcgcgcagagcgaa	Protospacer
  * **********.************ ***. **..

259. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MK061410 (Gordonia phage Eyes, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgcgctgccgccaagaaggccccggccaagaagg	Protospacer
 . .* .*************  ***********.

260. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MK967377 (Gordonia phage MagicMan, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgcgctgccgccaagaaggccccggccaagaagg	Protospacer
 . .* .*************  ***********.

261. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to KU998235 (Gordonia phage Bowser, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgcgctgccgccaagaaggccccggccaagaagg	Protospacer
 . .* .*************  ***********.

262. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NC_031255 (Gordonia phage Schwabeltier, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cgcgctgccgccaagaaggccccggccaagaagg	Protospacer
 . .* .*************  ***********.

263. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050092 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

264. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050081 (Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

265. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050098 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

266. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050104 (Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

267. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP025013 (Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

268. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP049731 (Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

269. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP053440 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

270. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP018229 (Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

271. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP025507 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

272. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP016287 (Rhizobium leguminosarum strain Vaf10 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

273. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050109 (Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

274. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP048281 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

275. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP030761 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

276. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP054022 (Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

277. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NC_012848 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

278. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022666 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

279. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP054032 (Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

280. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP022565 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK01, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

281. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP053206 (Rhizobium leguminosarum bv. trifolii TA1 plasmid pRltTA1D, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

282. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP041605 (Streptomyces sp. S1D4-14 plasmid pS1D4-14.1, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cacgagatacccaagaagacgacggccaagaaga	Protospacer
 * . **.  ********.**.************

283. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP050086 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
attgccgccgacaagaaggcggcggccgagaaat	Protospacer
*  .* .*** ****************.****. 

284. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to AY526908 (Bordetella phage BMP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga------	CRISPR spacer
aagaagacccccaagaaggcggc------gaagtccgccc	Protospacer
**** **** *************      ****       

285. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to AY526908 (Bordetella phage BMP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cactcgaccaccaggaaggcggcggccactacaa	Protospacer
 *  *****.***.**************  * .*

286. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NC_005357 (Bordetella phage BPP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga------	CRISPR spacer
aagaagacccccaagaaggcggc------gaagtccgccc	Protospacer
**** **** *************      ****       

287. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NC_005357 (Bordetella phage BPP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cactcgaccaccaggaaggcggcggccactacaa	Protospacer
 *  *****.***.**************  * .*

288. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to AY526909 (Bordetella phage BIP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga------	CRISPR spacer
aagaagacccccaagaaggcggc------gaagtccgccc	Protospacer
**** **** *************      ****       

289. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to AY526909 (Bordetella phage BIP-1, complete genome) position: , mismatch: 9, identity: 0.735

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cactcgaccaccaggaaggcggcggccactacaa	Protospacer
 *  *****.***.**************  * .*

290. spacer 15.3|7102791|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_012520 (Rhodococcus opacus B4 plasmid pROB01, complete sequence) position: , mismatch: 9, identity: 0.75

acgtcgactgtggccccggcccggagcccaccgccg	CRISPR spacer
gcaggggtggtggccccggaccggcgcccaccgccg	Protospacer
.*.  *.. ********** **** ***********

291. spacer 15.9|7103230|34|NZ_LN831790|CRT matches to NC_019202 (Pseudomonas aeruginosa plasmid pKLC102, complete sequence) position: , mismatch: 9, identity: 0.735

cacaccacgtcggtggccagggtgtgttggcctc	CRISPR spacer
ttcatcaagtcggtggccagggtgtgccggaaac	Protospacer
. **.** ******************..**   *

292. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 9, identity: 0.743

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggcggccca	Protospacer
 *  *** **************.****** * *..

293. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.743

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggcggccca	Protospacer
 *  *** **************.****** * *..

294. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.743

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggcggccca	Protospacer
 *  *** **************.****** * *..

295. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to HQ711985 (Pseudomonas phage vB_PaeS_PMG1, complete genome) position: , mismatch: 9, identity: 0.743

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
gaaatcgcgacgctgcgcaaggcggccgaggtgaa	Protospacer
.* . ** ********************** * . 

296. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_023316 (Streptomyces sp. 14R-10 plasmid pZL1, complete sequence) position: , mismatch: 9, identity: 0.743

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
gcggccgctgcgctgcgcgaggcggccgaactcgc	Protospacer
.  * **  .********.**********.*****

297. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP038257 (Microbacterium sediminis strain YLB-01 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
aggcgagaagcgcagcgccaggcggccgagctcgc	Protospacer
*.  . **..*** **** ****************

298. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR134456 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence) position: , mismatch: 9, identity: 0.735

gacgactcgggcaccgtcgccgggatcgtcaccg-----	CRISPR spacer
accggcacgggcaccgtcgccgggat-----ccggcagg	Protospacer
. **.* *******************     ***     

299. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013856 (Pseudonocardia sp. HH130630-07 plasmid pLS2-2, complete sequence) position: , mismatch: 9, identity: 0.735

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
gtcgacccgggcaccggcgccgggatggccctgc	Protospacer
* ****.********* ********* *.* .  

300. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP010421 (Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence) position: , mismatch: 9, identity: 0.735

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
cttggcttgggcaccctcgccgggatcgttgacg	Protospacer
  .*.**.******* *************.. **

301. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to NZ_CP010410 (Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
tccgctcctgccaagaaggccccggccaagaagg	Protospacer
   .*  *.***********  ***********.

302. spacer 13.1|5460396|34|NZ_LN831790|CRISPRCasFinder matches to MT708548 (Streptomyces phage Salutena, complete genome) position: , mismatch: 10, identity: 0.706

aagacgaccgccaagaaggcggcggccaagaaga	CRISPR spacer
cccgcaccggccaagaaggcgccggccaggaagg	Protospacer
   .*. * ************ ******.****.

303. spacer 16.2|7112304|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 10, identity: 0.714

agcgcgcgggtgaagatcggcatcacggccggctg	CRISPR spacer
tggtcgctggtgaagatcggcaccacggcggcgca	Protospacer
 *  *** **************.****** *  ..

304. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049317 (Caballeronia sp. SBC2 plasmid pSBC2-1, complete sequence) position: , mismatch: 10, identity: 0.714

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
ctaggcgagacgctgcgcaaggccgccgaggataa	Protospacer
   *.****************** ******  .. 

305. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049157 (Caballeronia sp. SBC1 plasmid pSBC1_1, complete sequence) position: , mismatch: 10, identity: 0.714

aacgacgagacgctgcgcaaggcggccgagctcgc	CRISPR spacer
ctaggcgagacgctgcgcaaggccgccgaggataa	Protospacer
   *.****************** ******  .. 

306. spacer 16.6|7112595|35|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NC_017805 (Deinococcus gobiensis I-0 plasmid P1, complete sequence) position: , mismatch: 10, identity: 0.714

aacgacgag-----acgctgcgcaaggcggccgagctcgc	CRISPR spacer
-----tgggcgcgcgcgctgcgcaaggcggccgtgcccgc	Protospacer
     .*.*     .****************** **.***

307. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 10, identity: 0.706

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
aagcgcgatagcaacgtcgccgtgatcgtcaccg	Protospacer
.*  .*   .*** ******** ***********

308. spacer 16.10|7112884|34|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 10, identity: 0.706

gacgactcgggcaccgtcgccgggatcgtcaccg	CRISPR spacer
aagcgcgatagcaacgtcgccgtgatcgtcaccg	Protospacer
.*  .*   .*** ******** ***********

309. spacer 15.6|7103012|36|NZ_LN831790|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP046573 (Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence) position: , mismatch: 11, identity: 0.694

actccgcccgcggccgcgaaccgcaccgactccctc	CRISPR spacer
cgaacacccgcgaccgcgaactgcaccgactcttcg	Protospacer
    *.******.********.**********... 

310. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to KC900378 (Pseudomonas phage LKA5, complete genome) position: , mismatch: 12, identity: 0.647

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
gctaactcgccctggagccggtcgcgctcggcga	Protospacer
 ..  ******** **** **********     

311. spacer 2.3|2517342|34|NZ_LN831790|CRISPRCasFinder matches to MT118301 (Pseudomonas phage Epa33, complete genome) position: , mismatch: 12, identity: 0.647

ttcttctcgccctcgagcaggtcgcgctcccact	CRISPR spacer
gctaactcgccctggagccggtcgcgctcggcga	Protospacer
 ..  ******** **** **********     

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	101352 : 142427	38	Acinetobacter_phage(16.67%)	transposase,integrase	attL 109132:109149|attR 152353:152370
DBSCAN-SWA_2	2005371 : 2058129	36	Hepacivirus(20.0%)	tRNA,tail,protease,plate	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_LN831790|101352:142427|DBSCAN-SWA
GTTATGCCGCGAGGGCGTGCTGATGCCGCTGCCTGGTCTCGGCTGGGGTGAGATAGCCGAAGGTCTTGTGCTTGCGCAGTCGGCGGCGGTTGTAGAAGGTCTCGATGAAGTTGAAGACCTCGGCGCGGGCGGTGGCCCGGTCGGGCCAGGTGCGGGTGCCGATCTCTTCCTTGAGCAGGGCCCAGAAGCTCTCCGCGGCGGCGTTGTCGAAGCATGATCCCGTGCGTCCGCAGCTCTGCCGGAGCTCGAACTTCCCTATTCGTTCCCGGAACTGGGTGGAGGTGTATTCGCTGCCGCGATCGCTGTGAATCACGCAGCCGGGCTCCAGTCCGCCTCGGCCGTGGGCCATGTCGAGAGCACCGACGACGAGCTCGGCGCGGTGGTGGTCGGCCATGGCATAGCCGACGACCTCGCGGGTGGCCAGGTCCAGCCAGCAGGCGAGGTAGAGCCAGCCCTCGGCGATGGGCAGGCAGGTGATGTCGCCGACCAGCTTGGTGCCGGGGCGCTCGGCATGGAAGTCGCGGCCGATCAGGTCCGGGGCCGGCTGCGCCTTCACATCAGGCCGGGTCAGCGAACGCCTCTTGCGCCGGGTGACGCCACGGATGTCGCGCTCGCGCATCAGGCGGGCGACGCGTTTGCGGTTCACCCGTCGGCCCAGGCGGCGCAGTTCGGCGTGGATCCGCGGGACCCCGTACGTGTGCCGGGACGCGATGTGCACCACGGCGATCTCGTGCGCGAGCGCGTCGTCGGCAGCCTGACGAGCGCGGCGGGCGGCCTCGCCCTCGCGCCAGGCGTAGTAGGAGGAGCGGGAAACCTTCAGCACCCGGCACAGCAGGACGATCGGGTAAGCCGCCTTCTCCGCATGAATCAACCGGTACAGCTCGCTCACCGGTCGTTCTCCTTCACGAAGAAGGCCGTCGCTTTTTTCAGGATCTCGATCGTCTGCTGCTGTTCACGGACCTCCTTGCGCAGCCGCTTGAGCTCCTCGCGCTCGGCGCTGGTCAGCTCGCCGGACCCGCCCTCGCCCCGGTCCGCCTTCGCCCAGCGGTACCAGCCTCGCAGGGACTCGGAGCTGATGCCGAGCTCCCGGGCGACGGCGGTGACCGTTTTGCCCGAGGAATCGACGAGCGCGATCGCGTCCCGCTTGAACTCCTCGGTGTACCGCTTCGTGTACTTGCTTCCCACCTGGTGCTACTTCCTCTGGAACCTCAAGATCCCAGTCTCCAGGTGTCCACGATCAAGGGGAAGCTTCAGCACCGAGCTGCACCTCGCGCCGGCACTCAGGACAGTCCGGCAGCCACACAGCACGGGATACAGCCGCCGCTCCAGGCCGTCAGGAACTTCGCAAAGATTCACCCTGCCGAGCCGAAGTCAGTAGCACCGTCGTGGCATCTGCTGAGCAGCTTCCGCGAGGCACCACCGCTCCTGGCCTGAGGCGGTGTTCGCGAGTGCTGTAATGTCACCTGCAGCAACTATGGGAATCTGCCGAAGACTTGGAGTGCTACATCATGCCTAGGAGAAGTACGCCTCCGGGGTACTGGATAGGCGCCCTACTCTTGGGTGCATTGTCGGTCGTGCTTGTGCTTGCCATGCAAGCGAAGCAGAACCTCCCCGGCCATGTATCACAGACAGGCGATGCCAAGCCCACCGCTAAATCTTCTCCGCCACTCCCTCCTGAAGCGCGATACCCAGTACCACCTGATACTGGCATGGGTCGCCGAGTGGTGTATTCAAAGAAGCAGCAGCGGGTTTGGTTGATTGCTGAGAATGAGCAAGTCCTGCGCACCTTCAGGGTATGGCCTGGCACCATAGACCCGGCAGTGGGTGCCCACACTGTGACCTACCGGCGTGCACAAGGAACCGGAACTGATGGTGCCATGGTAGAGAACGTAGTCTACTTCGGAAGTAATTACGCCTTTTCCAATGCAGTGGACGGCTCGCCGCCGAAGCCAAGCCCCGGCCTTCGTACCGGTGCCATACGCGAGAGTGTTGCAGATGGGCGGGCGATGTGGAAGTTCGCATCCGAAAATACATCTGTCTACGTAGCTGAATGACCATTTTCTTTGGCCAGCACCTCGCGTGCGGACCTCTCTCGCTGCTTCATTTGAGACAGTACGTCCTGCAATGCACTTTCATGCTCAGCAATCTTTTTTTCCTCGAGAGCCACTTCTCCCTCGAACCACATCTGCACGACACCAGATGACTTCTTACACTCGACGTCTCGGGTAGCAACGGAAACTTCGTGCGGAGTTGCTTTTGCGGTTTTCCAGTTCCACTTTGGGTCGTTCATGGCATCCATCGGTGAATCGTATTTATGGCCCGTCTCAGCCATGCAGTCAGACCAGCCCTTAAATGCCTTCACGACGGAAGGCAAGCGTGTGGCAGCAATATAACTGGAGGCCTTTATTTGCTCTGGAAGATTCTTGTCCTCCAACTGCGGAATACTCTCCTCCGCCTTGTCCGAGCACGCGCTCAACGCCTTAGACTCCTGCGGATTAGGTGATATAGAAGGCTGCGATCCTCCTCCATTCAGCACTGCCATGTAGTGATAACCGTGCTGCGCCTGCTTCTGGTTGACGGGGCCGTATCGCCCGGCCATAAGTGTCGGCAATTTATCTGGCGTTCGACGCGGCAGCCTGAATTTGATGCGCTTATCAGCCAAGCACTTATCGACAAGTGCCATCGCCGCCTGCGCGACGAATCTCCTCTGATCGTCTGACTCGATGTACTTCTGAATCGGCAGCACCAAATGCGGTAGAGGGTCGTAGATGTCTGAATCGCGCTCGGCTTCCAGTGCAGACGGGCGAGCCTCCGCCACCGACCCCGTCGCATCGCTTTCGTGTGAGCACGCCGAAATGAGGGTTGACGTTAGGACGCAAAGTGCGAGGTGAGTAAAGTGTCGACGCTTCATATACATGCCTCAAATCGCGAAAATTACAGAAAGGAGGCTGACTCCCGCCCTGCTCAGGGCGGGAATCAGCCTCTTCACTCATCAGTAGTAGTACGACCGCCAAGATGCGTTCTCGTTGTAAGTCTTGACGAGCTGTACGTTGGTGTTGGAGGTGACGACGTCATAGTCACCCTGCTGGCCGGAATAGAAAAACACTCGAACGAAGTCGTTGCTGCAGACGCAGCCACCCCCCATACTGTAGGAAGCAGACGCGGCGTTGTTCTTGACGGGCTGGCCGGCTCCTGCCCCGTTGTTCGGGAAGACGTACCCAGCCAAATCGTCGACTTCGCCCGTACCACTACCCCATCTGTAATATGCGCCCTGCTGGTTCGAGTTGTAGTAAAGACAGAATCCGATTCCGTTGGCGTCCATCGGACACTTGCCTGTGGCAGCACTCGCCGGAGCAGAAAACGCGAAAGTAGAGGCCACGACCGTTATGGCCATACCCACCACTGCGAAAATTTTGCGCATTAAACGATCCCCCTTCTTGGGATTTTTCACCTTCATCCTAGCTTCACTAACCTGCAAGATCAATCACTTTCTTCTCTGTCCATATTTGCTGCCATTGGTGTCATTTATGGAAGCTGCACCAGGCTCATGATGAATGGCTGGGTTTTCTCACGTAGACTGGTCGAGCCAGTCCGCACCAGGCTCCGCACCTGCCCCTGATCGACCAACTTTCGCACCGTAAGAGCGATACACTGCTATATGTGGCATTTTACAAGGATGGCGAGGAATTGATACCAATGCATGACAAGGAAGAGAGGGTTTCGCGTGAGTTGTCTGCCGTTGCGGCCGGTTTTACGGTGAACAATGCTGCGCTCATTAACGGCGGCATCGCCGCAGGAAAGGAAAAGTTGCGGCGTAGACGAATAGTGATCGCGGTATGCTCTGTAGCAATCGCGCTGCTCGGCATTGCAGTGATGGCTGGCGTAGACCTCTACTGACCCCGATCAGTGGCGGATGTAGACGTCACTGACTTCGGCTCGGCAGGGTGAATCCCCGCCCCCACCCGCATACCTCACACAGCACGGACCGACTCCAGACCCTCCCACCGAGCGGCAGCACGGGGTGACGGTCCTGCGTGAGCTTGCCGAGCCGGAGGTCGGCGGCTTCGGCTGGGGGTACAACGGCGGCGGCACCAGCGCGGCGGCCGCGGCGATCCTCGCCGACGCGCTCGACCTCGGCGACCCGGACAAGTGCGGCATCGGATACGCGACCTACCCCGAGGACGAGGTCCTGGCGCAGCTCCGGGAGGACTTCTGCGACGACGTCCTCTCCCAGCTCTGCGACCAGTGGCGGGTGCGCCGCGGCGTCGTCCTGCGCTGGTCGCTGGCCTGGTGCCTGCAGCGCGGCATCGACGAATTGCCCGCCGCTCTGCGGGAGCTCCCGCCGCTCCAGAGCCAGAGCTGACCGATGGGCTCGCCGAACACAGCGCGACCGGGCGGCTCCCTGTGGACCCGCCTGGTTGACGCCTTCCACGGACGGGACACCCCGGCGCCCACGCCACCGGCCGTCCCGTGGAACAGTCTGGAGTGGAGGGTCGACCCGGAGTACAGGTCGGAGCGGTGGTCGAAGGTGCCGGCGAGTGCTTCGGGTGCCATGTAGGCCGGTGTGCCGATCAGGACACCGGTGGTGGTGACGTCGTGCTGGCCGTCGTTGCCCTTGGCGATGCCGAAGTCGACGACCGTCGCCCTGCCGTTGCTCCGGATCTCAACCATGGAAGAGTCTGAACGCGTCCTGTCCCTACGGCAGGTATGGCACCGCCTGGGTGATCGCCCAGGCGGATCTCAAAGGAGAGTCCATGCGTATACCGCGATGGATCACGGCAAGCCTCTTCACCACGGCGGCAGCCGTGTCAGCACTCGCCCTGAGCTCGGGCTTCAGCCTCGCGAACAACGACAGTCACCACCGCGACTCGGTTACGACGGCCGGGCAGTACACCACCCTCTGCCTGAACGGTGGCTGCGCCGACTGACCCACCACCCCGCACCGACGCGCCGCAGACGTGAGGCGGAGGGACTCACCTCGTCAGGTGGGTCCCTCCGCCACCTCACGCGGCCTGCCCCAGCCGAGCGCGGCCAGCACCACCACCTTGTCCGCCGTCAGCTTCCACGGCCCCGCCGGCCGCTCGCCGCTGAACGTCCAGCCCTGAAGTGGGCGGCGTAGGGAGATGACCGGGAGCGGAGGGCGGCCAGCTGCTGGAGCTGGTCCGCGGCGAGCTTGCCGCGCTGGACTGCTGGCTGGCGCCTTCCCCGAACACCTCACCGGCACCGTCCCGCAGCCGGGCCGCGCGTGGCTCGCCGCCGAGCACGCCGGGACCGTCGCGGCCGCGGCCAGGCCGGCTCTGGACGCGATGGTGCGCCTGGCCGACCGCGGTACCGGCCTGCTCCTACGGCGCCGGTGTGCGCCGTGCTCGCCCCGGCGGGCCGCTGACCGCCCGGGGAGACCGGGCTGGTCAGGACGAGAAGCGGACACTGCGCCGGCCGGACGAGTGGGCGAGCACGGTGTTCCTGCCGGCCCGGGACCGGACTGGATCCTCGCGGCAGGACTCCTGCTCGCGAAGCGCGTCAGGAGACCGTGGGGAGGTGCAGGTGCCGAAGCATGACCGCGAAGTTCGGGGAGTCCGGGAACGGCTGACGATGACCGACCTTGGCGTACCCCCACGCCTCGTACAGCGCCTGCACCTTCGGGTGGTCGGGATCGACCAGGAGCACGGCCAGGGCCTCCGGCCGGTCCTCGAGCAGCGCCGTGTGTAGCCGCTCGGCGGTCCCCGTCTTCCGCCACCGCGGGCGCACCATCAGCTCGGACACAGAGAAGGTCGAGTCGTTCGCCGGTGGCTCGCTCAGGTGCTCGCGCCACCACTCGCGGCCGGGGGTGGCCGGGGCGCCGTATGCGAAACCGACCGGTTCGTCGCCGTCGTAACCGATGACGCAGGCAAAACCGGGGTGCTCGCCCCAGTGGTCGACGAACCAGGGGAAGCGTTGGTTGAACTCGTCCATCTGGTCCGCGTAGGCGTCGGCGTGCACGTCCAGCAGTGTCTGCCGGATGGCCTGGAGGTCCTCGTGGCCGAAGCGGCGCAGTTCGACGGCTGTCGTGGTCAAGGGGTGCTCCATTCGGTCCGGTAGTGGTCGGTCCATTCGTGTGCGATGTGGGCGGAGGGGGCGCGGGCGATCAGGTCGCGTTGGAAGTCGCCGAGGAGCTGCCGCATTCGCCCGGGGAGCGGGGCGCCCGCCATGATCGCGAAGACGGTGCCGCTGGTGGCGCAGGCCTGCTCGATGTCGTCCTGGTGCAGCTGGGCCAGGGCGAGGCGTGCGGTTGTATGTGCCCGGTTGCGGCGGTAGGTGTCGGGAAGGGCGGCCAGTGCCCGGTGGGCGGCGGCCTCCGCTTCCGCCGGGTCCCCTACGACGTCCCGCACGATCGCGGTCAGGGAGTGCAGCTCCGCCCAGCTGTAGAAGGCGATCCATGTCGAGCGCGGCTGTGCCGGATCGGTCTTCGCCAGGGCGTCCTCGGCGCGGCCGAGGCAGCGCAGGGCTGCGCTGCGGTCGCCGCTGTGAGCGAGGCCGACGGCCATGCGTGCCTGGGCGAGGGAGGCGTGCAGCGGGCTGCGTCGGACGATGGGTGTGGCCTGGGCGGCCTGGGCGGCGGCGACCGCCTCGGGGTAGCGCTTGCGCTGTCGGGCGAGCATGGCCCGCAGGTTCCACACCTGCATGGCCATCTCGGTGTCCTGGGCGAGGCCCGCGAGAGTCAGGGCGCGGTCGAGGTGTTTGCCGGCGCCGTCGAGCTGCCCGGCGTCGATCAGGGCCCACGCGGCGGTCGCGGTGAAGTCGCTGGCCAGCGCGTACAGGCGCTGCCGTACGCGCTGGGTGGCAGACTTGCTCTGTAGGCCGAGTGCCTCGTCGGCGCCGGCCAGGGCGGCATGGGCGAGGCTGCCGTGCCCGCCGCGGGCGGCGTCCAGCGCGACCAGCTTCTCGACGTCGTCCCGCAGCCTGAGCACGTCGGAGGTGCCCACACGTGAGCGGGGCGCGGGGGCGGGCATTACGGCGGCGGCAGCGGCGCCGGTGGCCGCGCTGCAGAACTGACGACGGCGCACGTCGGGGTCCTCCGGTAGTGCTGGTGGGACAGTCTTGTGTCTCCCCCGGGGTACGAACCCTAGAGCTGTGGGGGAAAGACCGGTGACCATCTCCAGGGCCCGGCGCTGGCGGTCCTGGGGCCACTGGTTCTCGCCGGACAGCCACCGGAACACGGTGCGCTCCGACGTCGCGCCGGCCCGGCCCGTGAGCTGGAGGATGGCGTCGTTGACCGCGTCGGCGAGTTCTCCGGCTGACATCTGGTGCCCCGTCATCCAGGCGGCTAAGTCTTCGTTTCTGGTCTCCGCCACGACAGCACCGTAGGGCGTGGCCGAGACCCAGCGCAGGTAAAGGGCTGTTCAATTCGTCAGTACGAGGGCGAGCATGCCGTCCTGCTTCGTCATGCACGTTGCCCGGTGCTGGCCGGTTGGGTGTGGTGTACGGCCCCGCCGCGCCTCTCCCCCCTGGGCGCGGCGGGGCGCCGACTCGATCAATCTGCTGAGGCAGCGATGACCAGTGCAGGAACCGCCCAGGAGACCGCCGCCGCACAGGCCGCTGCGGGCCCTGCCGCAGCCGTGCTGTATGTGTGCGCCGAGCGGGGAAAGTTGAACCCCACCCTGGCGGAGGAGCGCGCCGAGGAGGAAGGCCGCGCCTTGGCGCAGCAGCACGGGCTGACGATCACCGACACCGTCAGGGACGAGTACGGCGAACCGGAGCCCTGCCTCCGCGTCGGCTGGCAGCGCGTGCGGCAGCTCGCGCAGTCCGGCGCGGCCGCTGTAGTGATCACGCGGTGGCCCACGTGCATCGCACCGGAGTCCTCCCGCGAGCTGCGCTACCGCGAGATCCGGTGGCTGCAGGAGCACGGGGTGCGGGTGCGGTACTCGTGGGCGCCGCTGGCCCAAAGCGGCGGTGAGGCCCGGTGAGCACCACGCACGGTCTGCTGCACGGGGACCACCGCTGGATCGGCCGCGAGGTCGAGGACACCGCCTCCGGGCGCCGGGGGATCCTGCGTGCGATCGCCCCCGAAGGCGGCAACCCTCGCCCGGTGGCGTGGCTGTGGCCCAAGGGCGGAGGAACCGAGTGGACCACCGACCCGGCCGCGCTCGCCAATCCCGCACCCCTCACGCCGGACGACTACCGCCGGGAGGAGCGATGAGCGGTGTGCACGCCCGCCCCTCCCGGCCAGGCCGCGCCGTACTCGCCCTCGCAGCGCTCGCCCTGCCCCCTCCCACGGTCGTACTTGCGCCCCGCTTGGGGGCCGCTCAGCTCCCGGCACCCGTTCCGGACGTCGGCCCGCCGGACGCTGCTCCCGAGGTGGGCCTGCAGGCTCAGGATGACCGCCAGCAGGATGACCGCCAGATCGACCGGACCGAGCGGCGCCCCGACCGGTACGGTGCCCGCCCTCACCTTTCCCGGTGGTCCGCACCGTGACCGGGCGCCGCCGCAGGCATCGGCGCGGCGGCCCGCCGTGGTGGGCCTGGTGGCAGACCTGGTGCTTGTGCGGCGCGCTCCTCGCGCTGGTCCTCGTCACTTTGCTTCCTCTGTAGGCCCCGGCTGAGCCGGGCCGGACGTCACACCCCCGGCTCAGCCGGTTCCAGTTTCTGAGTGGGAGACACCCCATCCCCATCCGTGCTTTGCGCGGGGCTGGGCCGGCCTGCTGCCCGTGCCCGTGCCCGGCGGTGACATCCCGCGTATCTCCGCAGGATGGCCGCATTCGGGCCGGTGATGGTGGGTCGTGGGCTGGGTCCACCTGCATGATGCAAGACCGTGCGCCCGAGAGCCGGCCTAGAAGTCGGGCACCAGCTCCACCGGGCCCGGCGAGAAGTTGGCGAAGCACCCGCCTTCCGGTCCGCCATGACGGCCGGGCCGCAGGCGTTGGCACCTTGGACTGGGAGGTATAGATGAGCATCATCCTGATGTCCGACCCGCGCGTGGCCGCCATCCCCGTCGCCGACTGCGGCGAGCCGCTCGTCGACGTCCGCGAGTCTCTGCTGGTGGACGACCGCAAGGCCGACGCGGCAGACGCCTTCGTCCACATCCGTCAAGGCGTTCTCGACCGGCTCCTTCACGCCCAGTCGCTCCTGCCCGGCGGCCTTCGCCTGCTGTTCATCGAGGGCTACCGCCCGCCCCACCTGCAACGGCGTTACTTCGAGCAGTACGCGGACGAGCTGCGCACCGCCAACCCGGCCTGGACACAAGAACAGGTACATGAAGCCGCCAGCCGGTTTGTGTCCCCGCCGGAGATCGCGCCTCACAGCGCCGGGGCCGCAGTCGACCTCACCCTCGTCGACGCCGACGGCCGTGAGCTGGACATGGGCACGCGCGTCAACGCCAGCCCCGAGGAGAGCGACGGCGCCTGCTACACCGACGCCCCCGGCCTCAGCGGCCGGGCCCGTACCAACCGGACCACGCTCGGCAGCGCGCTGTCCTCCGCCGGGTTGATCAACTACTGCACGGAGTGGTGGCACTGGAGTCTCGGCGATAGGTACTGGGCGCTGCAGACCGGGCAGCCTGCCGCCCTGTACGGGCCCGTCGACCTGCCGCAGAAGCCCCGCGTCAGTGGCCGTTGACGCACGAGGAGCGACCTCTGGGGACTCCCCCGAGACCAGTTGGCCGCATCATTGCAGGCCCGTCCGTGCCACCCGTTCGGGAAGGAGCTTCATGACCACCGCGTCCACCGCGAGCGTGGGCTACTGGGAGCCGCTCTGGGCGCAGGGCCGCCGATACCGGCAGCTCGATGACGCCGAGAGGCAGCTCATGAAGGAGCATCTCGGTCCCGGCCGCGGTCGCCCGGCCCTCGACCTCGGCAGCGGCACCGGTTGTGTCGGCAGAGACCGTGTCCCCCGCAGGTCGTGTCGCTTTACGCAGTGGCGAAGTTCCAAGCGCCTGTCGCGTTGCGGCGACTCATCCTGTTCCTTTCCCACCTTGGGGGGTGATCGAGATCACTTCGACCGGCGCGGTCGACCAACTGATATGACGGGAGGCTGCGCTGCTCGCTTACGGTCGACTCTAGGAGGTGTAGCGACGCCTCCCACCGTGACAACACTCGCGACTACGAGTGAGACCGTCTACGCGATCACCGGCCTGCACCCCGAGCAGTCCAACAGCCCACATCGCTGCCCGGCCCGCGGGAATTGGACCATGAAGAACACCGTCCAACAATGGGGCCCACTACGACGACAAGTCTCAGGGCAGGACCCGCAACACGCCCGTCGCGCTCGCCACCGATGGCGCCCCGATCCGCAGCACGCTCAAGTTTGCTGGTGTATATGAACGCCGTCGACGGACACCAAGCTCACGCCGAACCGCGCCGTACCCTTACCTTCTAATACATTAGATGACTAACCGGACATTCGACGCGAACGCCGAGCCCGGCACCCGGGGTTTACTTTCGGCCGCCGGTCATCAATCGCGCGATCATGATGCCCGCACGGGGCGCCGTTGAGGCTACTTTGCGTGATCAAGCCAGTGCAATCTTGCGCTGGGAACTATCACTGTGGGTAGTTGATTCTTGGCGAAGTCCTTCCATCCTCCAGGGAAACCCCTTGTGACACCTTTGAGTGGGCTTGGGGATCTTTTCTGGCCGAGTGCGGATCGCATGGTTGTGCGAGGATCTTTGGCTGTGCAACGCTCTTGATCGAAACGGGGTGATAACGAGCTGGATTCATAGGTTCCATGCCGCGCTTTGAGCACGAGACAGAGACTGCTAAGCGCCGTAATTTGGGCGCTGCGTCGACGAGGTGCGCGGTCACTCAAATCGGGCAAGGTGGTCGCCGGCATCAAGCGAGACTGGCGTTAGCTTACCGGGGGATGCTCATATGAATGTCGACATTGATCACGTGCGCGCTCTGATGGTCGAAGCATGCCGACGGAGCGCGGTGCCAGCAGAGTCTGTGGATCTAGTCGTCGACCATTACCTTCTTGGGGAGACTCAAGGGAAGTACTCGCACGGCGTGGCGAAATTCTGTTTCGAGTCGCAGTTCTTCGGTGAGCGGCAGGGATCACCTCGCACGGTTCGCGAGCGCGGTGTGCTTGCCATCGTGGATGCCCAACGTGAGATCGGTCCCGTCAGCGCGGACCATGCGGTTCGGATAGCGGCTGATCGGGCACGTGAGCTGGGCGCCGGTATCGTCGGCATGATCAACACGCAGCGCTACGGGATTCTGTCGCCCTGGGCTGAACACCTGGCAAGGGCTGGCTTCCTGGGGATCGTGATGAACACCTCCCGTGCCGACAGCACGGTCGAGGGGGCTCGGACGCCCTTTCTGGGCGTGAACCCCATCAGCTATGCCGTGCCCACGACTGGCGAGCCTCTTGTGGTGGACATGTCTACTACGAAATCACCCATGGGTGTTCTTTGGGAGGCACGGCGTGGCGCCGCGCAACTGCCAGCCGAAAGCTTTGTTGATCTTGATGGAGATTTTACGGTTGACCCGCACCTTGCCGAATCAGCTATGGTTTTCGGCGGCCATAAGGGCTTTGCCGTCTCATTGTTGATCCAGATCATGACCGGATCTCTCTTCGGCTTCCCCATGGGGCCAGGTGTTGAGTCAACGTGGACCACCGGATATACGTTCATCGCGATCGACCCTTCCTTCGGCGGGGAACTTGACGATTTTCCGAACAACAATGCGAGGCTCGTCGAAGTGATGGAAGGCGTCGGTACGCGAGACTCTCAGCCCTTTCGGATCCCAGGACGTCGGAGCCGGGCTCACGTCCGCAAGGTCACGGCCTTGGGGAAGCTTGATATTCCTGACTCCGTTTATCGTAGACTGAGGGCAAGAGCCGCCGGCGACTTTGTATCCGACTGATATTCCGCCGTTACCCATGGGGGCGTGATGACAGCAGGGTCTATTGCGAAATTCCACTGGTTTCTCCCCACCGCCAGCGACGGGCGGTCCCTCGCGGTCGGTACGCATGGGACCCATGGTGCGGCCGCCGGTGGTGACCAAGCGCCCGAAGGCGGGGCGGATCGGTTCAGGGCCCCCGACATTGCCTACCTTGCACAGGTGGCACGAGCAGCCGAGCAGCAGGGCTTCGATGGGATTCTGACCCCCACGGGAACGTGGTGCGAAGACGCCTGGCTGGTCACCGCCGCGCTAGCCCGGGAGAGCGAGCGACTGAAATTCCTGGTCGCCTTTCGGCCCGGATCCGTATCACCAACCCTCGCGGCCCAGATGGCCTCCACCCTCCAGCGGCTTTCCCGTGGCCGGCTCCTGCTGAACGTGGTCACCGGCGGCGAACGTGACGAGCAGGCCCGTTTCGGCGACCACCTCAACAAGGACCAGCGCTACGCAAGGACTGGCGAGTTCCTCACCGTACTTCGGGGAGCGTGGAGTTGTACCCCCTTCGATTTCAAGGGCGAGTACTACGACGTCCGTGGCGCAACCGTCGCCGCACCTCCGAACCCGTTGCCTGAGATCTACTTCGGAGGTTCATCAGAGGCGGCGGGCCCAGTCGCCGCACGTCACGTCGACACTTACTTGACGTGGGGTGAGCCTCCCGCACAAGTGGCCGAGAAGCTGGCATGGATGAGGAGGCTGGCGTCCGAGGAGGGTCGAGCTCTCCGTTTCGGAATCCGCTTCCATGTGGTGGCCCGCGACACGTCCAGAGAGGCGTGGGCGGCAGCCTCACGGCTGTTGGACCGTATGGACAGCGCACATGTGGCCCAGGTGCAGAACGTGTTGGCAGCGAGCGAGTCCACCGGCCAGGCACGTATGAGAGCCCTCCATGAGACGTTCCGCGAGGGTTGGCGCCACGACGACCTTGAGATCTACCCAAACGTCTGGGCTGGCGTCGGCCTGCTGCGCGGCGGAGCGGGCACGGCGTTGGTCGGCAGCCACGCGGAGGTCGCCGACCGGATCGAGGAGTACCGGGCGCTGGGCATCGAGGAGTTCATTCTCTCCGGCTTTCCGCACCTGGAGGAGGCTTACAACGGCTAACACAATGAGGCGGATCACTGCTGCTTGCCGTGTCCAGGGCAGGAGTTGAGCGTTCCCCTCGTTGTGGGGACATCACCGTGGATCGTGTCGGATGAGCTGTGGGAGCGCTTGGAGCCGCTGCTTCCGCAGCGTGAGCGGCGCTTTCGGTACCCGGGTCGCAAGCCGCTGCCGGACCGGGAGGTGCTGTGCGGGATCTTGTACGTGCTGCACACCGGCATCCAGTGGGAGTACCTGCCCAGGGAGCTGGGCTTCGGCTCGGGCATGACCTGCTGGCGGCGGCTGCGGGACTGGAACGAGGCCGGCGTCTGGCAGCGACTCCACGAAGTTCTGCTCGCAGAGCTGAACGCGGCATCGCGACTGGACTGGTCCCGCTGCGTGATCGACTCCTCCCACGTCAGGGCCCTAAAAGGGGGCAGCACACGGGCCCTTCGCCGGTCGACCGCGGGCGGGCCGGCTCGAAGCACCACCTGATCACCGACGGGCATGGCACACCCCTCGCGGTCCTGTTGACCGGGGGCAACCGCAACGATGTCACCCAGCTGCTGCCCCTGCTCGATGCGATTCCGCCGGTCCGCGGCCGGGTGGGCCGTCCGCGCCGCAAGCCCGACGCCCTGTTCGCCGACCGGGGCTACGACCACGACATCTACCGCGACCGGGTCCGCGACCGAGGCATCCTGCCCGCGATCGCCCGGCGCGGCACGCGACATGGCACCGGGCTGGGTACCTACCGGTGGGTGATTGAGCGCAGCTTCGCCTGGCTGCACGGCTTCCGACGACTGCGGATCCGCTGGGAACGACGGGCTGACATCCACGAAGCGTTCCTCAAACTCGCCTGCTGCCTGATCACCCACCGACAACTCGGCTCATTGTGTTAGCCGTTGTTACTGGGTCGGTGAGGGCGTGCTGCCGGAACTGCGCCGTCGTGGCATCGCGCCGACGTCGAGCACGGCGGCGTGACCTGTGTGAACGCACATCGTGGAAGGGGGACCCATGCCGGACGACCTTGAAATTCCCACTCTTTGCGGAACCGGGGCCAATCTGCTGCTCTCGGTAGTCGATCTCATTCATCAGAGTGTGCCCAAGACTGTCTGGGAAACGGAGCGCCTCAGGAAGGTCTTCGGCAACCGGACCGTTCCCATGATCCTCGCCGACGGGGACGTGATGGCCTTTGGTCCGTGTCCCGACCGGACACTAGTGGCCTCGGCAGTGCTCCAGCGCCATGGGATTCGGCCGACCATCATCTACCACGAGCGAAGGGTGCCGGGCTTCACGCCCTCCACCGCGCACATCGCCATGGAGATATCCGTGGACGGGCGCACCTGGATGATGGACTTCGGAAGCCGCGAAAGTCGGCTGATCGAGGGAGAGTACTACTTCAACCCCGAGATCGAGGAGACGCTGGCCCTAGAGCGCTTCAACCTGCTGGACATGGACGTCGACCTGATGTCGGTCACCCCGAATCAGATGTTCGGGATGGTGGCCACCGAGAACATCGACATGGAACACAAGTACGACTACTACGAAAAACAGTCGCGCAGATACAGCGGGCAGATTTTAGAGGACCGGCTGGCCCTTGACAAGACGCATAGCGTCTACTACGAACTCTGATTCCCGATCAACTGCGCCTGTTCCTGCACGAAACGAGAGTAAATTGACCGAAGTGGCTTATGAGATCGAGCGTCTCGTAAAAGTCTATCCACGCCAGACCGAAGCCGCGACGAACGATGTCTCCCTGAGTGTCCGTGCCGGTGAGGTGTTCGGAATTCTAGGGGACAACGGAGCGGGAAAGACCACACTGGTAAGACAGATGGTCAACCTGCTGCGCTCGACTTCGGGTGAGATCAGATTGTTCGGCAGGTCGGTGCCCGGGAATCCGTTGTTCGTAAGCCGGACTGTCGCTTACATGCCGCAGAGCAGCATGGCGCTGAACCGTCTGAAGGTGAAGGAGGCCATTTATTTCGCCGCCCACCTACGCGGTATGTCCCGCCGCGACGCTGCCCGTGAACGCGACGCCATGATCGAGACGTGGCAGCTCGGACCGGTACGGGACAAGTCGAGCTCTCGCCTCTCGGGCGGGCAGCAGCGCCTTCTCCAGCTAGCTCTGGCCACTGCGGGCCGTCTGCCTGTCGCGGTGCTCGACGAGCCGACCAATGACCTGGACCCGGTCAACCGCAAACACGTCTGGGAGGTGCTGCGGAAGTTCAACGCCGAGCAAGGCACGACGATCCTCTTCATCACCCACGACGCGATTGAGGCGGAACGCATCGTCCATCGCGTCGGCATTATGAGAAAGGGCAGCTTCCTTGCGATCGGCCAGCCCGCTCAGCTGAAGCGGAAGCTTCTGGATCATATGCGGCTCGAAGTGTGGCTCCCTCCGGGGGAAGTTCCTGCGCTCCCTGCCGACATGCCTCAGCACTGGAAATCGGACGACAACGTCGTTCTGTCGGTTCCACGGGACCGCGCGCCCGCGCTGTTGTCCGAGCTGAGGCTGAACGAATCGATTGACTACCGACTCTACTCGGCGACTCTGGAAGACTTGTATCTGCACTATGCGAACTCAGACTGAACGGCCGGGGCTGGCTGCCCAATTCGTCGACCTCTGGCTCATGCAGCTCTCCAACTGGCGATGGTCCTGGCGTGCCATGATGGTTACAGGAATCATCACTCCCCTCATGACCGTCGCGGCGCTCGGGGCGTTCGCGAAGGGGCGGGGGCATGAGTCCCTCGTCTACGTACTCACCGGCAGTATTCTACTGTCACTGATGTTCGAGAACCAGAACAAGGTCGCCCAAAATTTCGCCTACATGAAGGCTATGGGGACCCTGGACTTTCTTGGTACTCTTCCGGTGCGTCGTCAAATGGTCATCACGGCGACGGTTCTGGCATTCTTCGCGCTTTCCGCGCCGGCGCTCCTAACGACTCTGATGCTCGGGTCGCTGATCCTCGGCGTCCATCTCTCAGTGAGCTGGCTGGTCGTCCTCGTCATCCCACTCTGCGTGCTGTCTCTGGCCGGTATCGGGGCCGTCATCGGGATTGTGACCCGAAGCCAGGAGGAGGCGAGTTCGCTCACCCTGCTGGTCACGATGCTTTTGCTGTTCTTCGGACCGGTGATTATCCCTGCGAGTCGGCTCCCCGGATGGCTGGTGACTATCAGCCACGTCAGTCCAACCACCTACGCGGCTTCGGCGATACGCCAAGTACTCGTCGGGCCGGTGACGGGACGGATCTGGCTCGACCTGTTCGTCCTGCTGGCACTCACCGGGATCACCCTCTGGTTCGCCGGCTCACGCATGCAATGGAAGGCCAACTGAAGGCAGCGTTATAGGAGGACATAATGTCTGAAACGCAGACGCTCGACGGTGTCTTGGCATCCACACGGCTCGCCTGGAGCGTGCTGTTCGGTGGAGAGTCGCTCGGCGAGGTCGACCGCGAGTTGCTCCGCTCGTTGCAGGACGACCCCGGCACCTGGGGTCGTCTGATCCTCGACACCTGGGCCACGTTCACCGCTCTCGACGGCAAGAGGGCACCTGCCGGACTCAGCGTCCGCCGGGATGCCGGCGCAGAGTCCGTGACCGCCACCGCCTCACGGACCGACTCGAGAGAGGAAGAGGCGGTGGCTCGGACGGAGGACGGCATGATCCCGGAGCAGGCGCAGTCCTCCTCGCAGCGGGCCGAGACCGTGGCGTCCAGGCCCGCGGAGCTCGCGGACCAGGCGGAGGGCCGGACCGGATCACCGGCGGTCATGGCGCCAGCGTCGTCCCGGCCGGAGCCCGCCCCCGCCGGGACGACGCAACCGCTCGACTTCTTCGACCCCGACGAGGAGGACGAGTCCGTACCGCCACGCCGGACGGTCACCGTCGAGGAGGTCAAGGCCCGCCTGACCGAGCTCATAGCCGAGATAAGCGGTTATCCGGAAGACGTCTTCGAAGACCACCTCGACCTGGAGGTCGACCTCGGCATCGACTCCATCAAACAGGTTGAGACGCTGGCCAAGGTCCGCGAGGAATACGACCTTCCTCTGGACGAAGGCTTCCTCATGCGCGACTACGCCACGATCGGGAAGATGGCCGGTTACATCGTGGACCGCCTGGAAAAGGAGACCTGAGCCGTGCGCGAGGACTTGCCAGGGTACGCAGGCAAGGTGGCGCTGGTCGTCGGCAGCAGCCGTGGCCTCGGGCGGCAGGTGGCCGAGCTGATGGCCGACCAGGGTGCGAGGGTTATCGTCAACTCCGCTTCGACCACGGTGGACGGCAAGAACGTCGCGCGCACCATCACGAAGAACGGTGGTCAGGCCCACTACGTCTGCGCCGACGTGGCCAGTGAGGATCAGGTCGCCGCCATGGCCAGCCTGATCCAGGAGAAGTTCGGCCGTCTGGACATCGTGGTCCACTGTGCGGCCGGCGGCTCGGAGGCCCGCGTCATGGATGCCACCTTCCCCATGTTCGAGCGCACCTTCCGCGTCAACTCCTACTCCTTGGTAACCCTGGCCCGGCACCTGTCTCCGCTGATGCCTGCGGGTTCGCGGTTCGTGTACATGAGCAGCATGGGGGCGATCCGGGCATCGCACGGGTACGGCGTCGTGGGCGCCGCCAAGGCGGCCAGTGAAGCCCTGGTGCGCTCCCTCGCCCTCGAGCTGGCGCCGTTGAACATCACCGTGAACGGAGTGCGCACCACGGCCTTCCCGAGCCTGTCGCTGCGCTACTTCTCCAAGGGCGGTGACTGGCTCGATATCTGCGAGCGCGAGTCCCCGCTGGGCCCACCGCAGGCCGGCAAGATTGCCGAAGCGATCCTTCTTCTGTGTTCGCAGGCCGCGGGCTACATCACCGGACAGGTCCTCAACGTGGACGGCGGCTGGCTCACCTCCGTACTGCGGACCCGAGGGGCCGAGGCCGACGTGAGCTGATCCTGCACTGAATCAACATTCAACGCCCCGGTCTGGGAGTGGTAGGAATGGAATTCGAACCGATCGCCGTCGTGGCTGCGGAGTGCAGACTGCCGGGCGCAGCCAACCTGCAGGAATTCTTCCGGAACAACCAAGAGGGGACCTGCTCGATCAGCAAGGCGCTCGACGCCTTCTGGGATGGCTGCGAGGTCTACGACAAGAACGACGGAGGGCACCTCAACACCTCGTACACCGACCTTGGCGGGTTCCTCGACCCCTGGGAGCTGGACCGCGGTGTATTCCGCATCGCCCCACGTGTCATCGAGCGCATGGACCCGGCCCACGCACTGGGCCTAGAAATGGCGCACCGAGTCATCGAGCAGGCCGAGCGGAGCGGGCCCTTGCCGCGGGACGAGACGGCAGTCGTCGTCGCCAATGTCGGGGGCGGCTCGACCAGCCGGATCAACGCGAACATGAAGGTACAGTCCGAACGCTGGGCCGGCGCGCTGCGCCGCCGGGAGCCGACCCTGGCCAACGTACTGGACGAACACCAGAACAATGAACGCACCCGCCACCCGGACAAGCGCGAGGACCTCGCCCTCAACGGGGAGTCCGGAACGATCGGTGGTCGCATCGCCAACTACTTCAACCTGCGCGGGACCCATTACGGCATCGACGCGGCATGCGGCAGCTCGCTCGCAGCGGTGCACTCCGCCTGCATGGGGCTGCACCAAGGTGAGTTCGACGCCGCACTGGTAACTGCCGTGGGGATCCTCACCCCCGACATCTTCGTCGTGAACAGTGCGGCCCGAACCCTGTCTAAGGACGGCAGCTTCCCCTTCGGATCCGCCGCCAACGGCCTGGTCCCGGGCGAGGGCGGAGTGGGCCTGCTGCTGATGCGGCTGGCGGACGCCCGGCAGCAGGGACGACCAGTGCTCGCCGTGACCCGCAGCATCGGCTACAGCACCAACGGCCGAACCACTTCGACCTGGGCTCCTTCCGCCGAGGCCGAGGAACGTGCTATCCGCAGGGCCTTCGACGGCATGCCCTTCGGTATGGAGGACGTCGACTATGTGGAGGCGCACGGCACCTCCACCCGGGCGGGGGATGAAGCCGAGTTCGACGCGTTGCTGCGCACCTATGGCTCGGTGACACGCTCCAGGCCCCTGCCGTTCGGCTCCGTAAAGAGCCTCATCGGTCACACGGTGGAGAGCGCCGGCCTGGTGGGCATACTCCGCGGGCTCTTCATCTTCGAGACCGGCACCCTCCCTCCGACAGTGAACGTCGACGACATACGCCCGGAGGTCGCCGGGGCCGCGGACCGTCTATGGCTCCAGCGGGCGAACGAGGGGCTCACCCCGGCGCCCGGACGACCGCGCCGTGTGGGTGTGAGCGCCTTCGGATACGGAGGCATCAACTACCACCTCCTACTGGAGCATCCCGGAACCGAGGCTGCCGCCATCAGCCGGAGCAACCCGCCGCTGCGACGCGACCGGACCCCCATCGCCATTGTCGGTTTGGAAGCGGTTCAGCCCGATGCTACGGACGCCGCCGCGTTCTGGCGCAATCTGCAGGAGGGGCTGGCGAGTCGGCAGGACCTGCGCGGCCGGGTGCCCAGCCGCGACTTGGATGTGGAGGACGCGGGTCTGCAACGCCAAGCGACCCACCTGCAGAACGCAGCGTTCGTCGACGTGCCCGGCACCGTAGACAACACGCGATTCCGCATCCTACCCAACCAGGTGCCTGGCCTCACTGACGAGTACCTCGTCCTACTGTCCTGTGCGGCCAACCTCGCGAGCGCGGTCGAACATGCCACCGCCGCCATCGACCCAACGCGAGCTGGCTGCATCATAGGTCAACTCCCGGACTCGGACCGCGAGTTCGAGCTGATGCAGTCCTTGCGGTTCATGCCCTGGCTGCGCCGGTTACGCAGACTCGCCCGCGCCCGCGGTATCGAAGCCCCATGGTCCGCGCTCCGTGACGATCTTTGGAACGACCCCACGCTCGAGCTCCACACCGTGAACCAGGACACCTCGGTCGCGGGCTTCGGCTCCACCCTGCCCTCGACGCTCGCTAGCTCCTTCGACCTGCGTGGCAAGAGCTACGCAGTACGCGCCGCCTGCGCGACCGGACTGGCGGCCCTTTCTCTGGCGGTTCAGGAACTGCGTGAGCACACATTGGACTTCGTGCTGTGCGGGGCCGTGGGCATGGGTGTGGGCCTGGTCAACCACACGGCGCTGGCCTCGATCCGGGCTCTGAGTGCCAACGGCGTTGGACGCCCGTACGACGAGAAGGGCGACGGCTTCATCATGGGAGGCGGTGCGGGACTCCTCTGTCTCAAGCGGCTGCCTGATGCGGAACGCGACGGAGACCCAATCTTCGCCGTCGTACGGGAGGTGCGTGGCGGCAGCGACGGCAAGGGACGCAGCCTGCTGGCGCCCAACACCGAGGGACGCCGCTTCACCATGGAACGCACATACCGAAACTCCGGGCTGTCCCCTGCAAGCATCACCTATGTCGAAGGCCATGGTGCCGCCACGGCTCTGGGTGATCGGTCGGAGGTCGAAGCGCTGTCCGCGGTCCTCGGTAACGAGGAGACGGTTTTCCTCGGCAGCGCGAAGGGCAATGTCGGTCACCAGAAGGGTGCCTCGGGCATGACCTCGGTGATCAAGACGGTGCTCTGCCTCCATCACGGTGAACTTGTGCCCACGCCGGGGTACGAGAATCCGCATCCGGCCCTCGAACTGGAGCAGCGGCGCTTTCAAGTGCTGACCGAGACGCGGCCCTGGCCCGCCCCGCGAGACGGTGCCCCTCGCCGTGCGGCCGTGAACGCGTTCGGACTCGGTGGCATCAACTACCACGCCGTGCTGGAGGAATACCTCCGGCCAGAGCCCTCGCGGCAATCAGCGGCGCGAACCACGCCGCGTGAGACGAGCCCGGAGCCCACCATCGCGATCTGGACCGCACCTGGCCAGGAGGAACTGGACCGCTCCCTGGCCGCCTTCGCCGAGCACGGCGAGGCTCCGCCACCGCCCGACTCGGCCCACACCCACCGCGTGGCAGTCGACGGGGGCACGGGCCCGGACGCAGCCAAGGCCCTGCACGACAAGGTCCGCAGGTACCTTGCCACCGGGCCGGACACGCTCACCCCCGCACAGTGGGACGCCATGGGGGTGTTCACAGGGCGAACGGATCTGCCGACTGGCGGCGTCTGCCGGCTCTACCCCGGCCAGGGCAGCCAGTACCCTGGCATGCTGCGCGAAGCGGCCCCGGCTATCGACGGCGCGGAGGACAAGGTGAGGGCCGCAGCCAGCGCGCTCTCAGCGCAACTGCCGGGACTGCTGGACGACTTCTGGCACGCCGACTTCGCTACATGCGAGCAATGGCTGTCCCGCACAGAGAACTGCCAGGTCGCCACCCTCGTGGTGAGCGCCGCCCTCGGTGACTGGCTCGACGGTCTCGGCGTGGCAGCCGACTTCCATCTGGGGCACTCCTTCGGTGAGGTCTCCGCGCTGGCAGCAGCCGGCGCTATCCCGCTGCCCGACGCGCTGCGCACCGCTCACCGCCGCGGCACCATCGCCGCTCAAGGGCGTGGCGGACCACGGCAGGGCATGGCCGTGCTGTTCACGTCAGCCGCAGAGGCGACTCGGTTCATCGGCGAGGACGACAACGACGTCGTCGTCGCCAACCGGAACAGCCGCCGCCAAGTCGTCCTCGCGGGAAACGCCGAAGCGCTCACCCGGGTGCTGAGGCGAGCGACCACCGACGGGATCGAGGCACGGGCACTGCCCATCGAGCGTGCCTTCCACTCGCCGCTGTTGCGGGACGCCATCCCCGCCTACCGTGCGTTTCTCGACTCGGTGCCCGTCACCAGCCCGCCGGCACCGGTGTACGAGACGCTCACCTCGCGGCCGTACCCACGGAACACCGAGCCCGGCAGGATCCGACAGAGCCTCGCCGACCAGTTTGTGCTCCCCGTGTACTTCGAAACCATGGTCCAGGACGCGTACGACCGTGGAGCGCGGGTCTTCGTGGAAGTCGGTCCGAAGCGGGCGTTGTCCTCCCTGGTCGGCGAGTGTCTCGGCACGTCGGCGAAGGTGCGCACCGTCACCCTGCTCCATCCCAAAGGGGGAGAAGTGGCGCAGGTGCGCCGTGCCGCCGCGCAGCTCTGGGCCATCGGCCTGACCGATGTTCGACCGGTCTCTGACGTAACTGCCCGAAAGGCCGCGACATGATCGGCTTGATCCCAACCGCCACACCCGTCGCCCTGCGCGAGGTGAGGCACGACCTGGCCGGCCGACGCGTGCTCGTGATCGGCGACTGCGACGGCCTCGCCGGGGCGATGCTAGCTCGGCTCAGTGCGGCCGGGGCCCACACCGAGGCAGTGATGGTGCGGGAAACCGTGCGCCCATACGCCTCGTCTCACCGCGGGCAGTTGCTCGCAGCGGAGGAGCTCGCCGTACGCCTGACCTCGGGGCCCCTTCCGGACTGGGTCTTGTTCCTGCCAGGATTCACCGCCCGAGCCCGCCCCGCTCAGGCGTTCCGCCCGGAAGAAGGGCTCTACGCGGGCGGGATGACACGAACCTTGTTCCACACGCTGTCCCCGCTCGGGCGGCGCTGGCTGGAGCGGGGCGCCGGCGGCTTCGCCGTGGTCACCCGCGCGGACGGCAGGTTTGGGCTGACCGGCGCCCGCCCGGGTGACCCGCTCGCCGGACTGCTGCACGGCACCGTGCGCGCCCTGCACGCGGAACTCCCGATGATCCGCACCGTGGCACTGGACGTCGGCCCATCGGTGCCCCTCGACGTCGTCGCCGACCGGCTACTCGACCTCGTCTCGGACACCTCCCATGGACACGTCGAGCGAGGGCTCGCCGGAAGCCAGGCGTATGCCACCACACTGGTGCCCGCCTTCGAGCAGCCCGCCGACATCCCGGGGGCCGAAGGCCGGTTGCCCTTGGAACGAGGCGACACCGTCCTGGCCACCGGCGGCGGGCGAGGAGTGACCGCTCGTGTCGTACGCATGATGGCCGAGGAGGTGCCGTGCCGCTACCTGCTGCTCGGCACCACCAAGTTGGTCGATGTCAAGGCGGCTCTCGGAGTGGGGGATCGCGATGAACTCCTGCACATGCCCGCGGAAGAGCTGGAGGCACACAAACGGCGCCAGTTCGCGGCGATGCGGCGTGACAATCCGACGCTGCTGCCCCCAGCGTTCGAACGCCACTGGGCCCGCATCAGCAATTCGCTGGAGGTCCTGCGGACCCTGACCCATGTGCGTGACCTGGGTGCCCGAGCCGAATACTTGTGCCTGGACATTACCGACGGGCACGCCACCCGTCGCTTCGCCGACGAACTGGTCAGAACCTCCGGGCCGGTACAGGCACTGTTGCACGGCGCCGGGGTGGAGACGAGCAAGAACCTGTGCCGGAAGACCCAGGACTCATGGGAACGGACCGTCGCGGTCAAGACAGCCGGGCTGTACAACCTCAGTCCGGTCCTCGGCGACGAGACCCGGCTGATCATGCTCTTCGGTTCGGCAGCAGGAACATACGGCAATCCAGGTCAGATCGACTATGCAGGGGCCAGCGAGTTTCTCACCACCGCCGCGTACCGCCTGGCCGCGGATTTCCCGGCTGCTCGTGTGCGTTCGGTGGCCTGGCCCGCGTGGGCCGAGGTGGGGATGGCAGTCCGGCCTTCCTCCCGGGCCGCCCTGGAACAGCGTGACGTCAGGTTCATGGAGGTGTCCGAGGGTTTGGACTGGGCCGGTGCGCTGCTGCGTAGTCCGAGTCGGGTTCCGGTTTGTGTCAGCCTCGGATACGAGGGAATGCCACCGGAAGCCACCGCCACCCGCGAGACGGCACCGTGGCGCTCCGCTCGCGCGAACCGGGGCAACCTGGTGGATCTGTGCTCCGAGGCGGGCCCCGGGCGCTGGGAGGTCCGGTGGACCTACCAACCCGAACTGGACGCGGCCTTGGCCGACCACCAGGTGGACGGAAACGTCCGTGTACCCTTCGCTCTCTTCATCGAGCTCATGTGCCAGACAGCCTCTGCCTGCCTCGGTGACCTTGGAGCATTCACCCTGCGTGCGCTGCGCATGCACCAGCCGCTGACCTTGGCACCCGAGCGCCCCAGGGACCTGCGGGCTGTGATCGCCCGCACGGCGGAGGGCACCCTGCGAGTCGGCGTGGAAAGCTCACCGATCCGTCCGGACCACAGCTGGGTGCCCGTCACCCTCCAGCATGCGAGTGCCGAGATCGAGCCCCTGACCGGACAGAAACCGGCACCCCGGATCGATGTGGCACTCAAGGGATTGGAGCCGGTCTCCGTGGACCACCTGCAGGAGCGGTTCGCCGCCAACGGGATCGTCTACGGCCCGGCCTTTCGCGAGATCGTCTCCTGCTGGCGTGACGGCGCGCTCCGCCTGGCCCAGGTACGCGCCGGAGCGGGCTGGAAGGCGGATGTGCGAGGGCGGTCCTTCTTCGACATCGGCCTGCTCGATCTCTCACTGCAGACGCTCGTCTTCCACCCGGGCGCCCGCCACGGAGGGCTGCCGACGGCGGTGGAGGAACTCATCGTGCACACGGAGCTCGGCGGCAGCCGCTCTGAGGGCTGGGCCTTGGTGGACACGGGCGCGGAGAAGCTGGGCGTGACCCTGGCCGACTCCGCCGGGCGGGTCATGGCCCAGATCCGCAATCTTGAACTGACCGCGCGCGAGTCGTAGGGCAAGGAAGGCTAAGTGAAGAATTTCCTCGTGATAGGCGTTGGTCCGCACGCGCGCTTGAACCACCTGCCATCGCTGTGGGCCGGTCAGTCAGCCGGCCTGGTCGGCCGCGTGATCGGTGTGGATGTCGCCGACGCGGTCGGTGACATCGCCGCCTCCAACTCGGCCGGCGGCACCCCTGAACTGTCAGTGACGTTCATCGAGCCGTTCGACGCCACGAGACGTACGCTGCCGGCCCCGGTGCGCAAAACCCTGGACTCCCTGGTGCGGGAGCACGCCGTCGACGCGGTCGTAATCTCCACCGAGCCGTCGTTCCATATGGTCTACACGCACTGGGCGCTGGGGCACGGCCTGAGTGTGCTGCTCGACAAACCCCTGAGTGTGCACGCCAATTGCTCTGTCGACCCCTTCAAAGCGTCGGCCATCCTCACGGACTTCGACGAGATCCTCGCCCGCTACGAGGCGGTTCGTAGGACCCATCCCGAGGTACTGGTGACCGTGCAGTGCCAGCGGCGCTATCATCCCGCCTTCCGCCATATGCGGCGGCTGATCGCCGAGGTGGCGGAGGCCACCAACTGCCCAGTGACGTCGGTGCAGTCGTTTCACAGCGACGGTCAATGGCGCATGCCGAACGAGCTCATCGACATCTCCTATCACTCCTTTGACCAGGGGTACGGCAAGTGCGCCCACTCGGGGTACCACTTCTTCGACATCGTGCCCTGGCTGCTGCGGGCCGGTGAGGCACCGGGCAAGGAACTCGACAGCGTCGACATCCACGCGAACTTCAGCCGCCCGCGCGACTTCCTCGCCCAGCTCGACGTGAACGACTACGCCCGTCTCTTCCCGGAGTTCGAAGCAGCCAATCCCTACACCCAGGCGCACCTGCTCACCGCCACCGAGGCGTTCGGAGAGATTGACGCGTTCGTCTCCATGGCCTACAAGAGCGGTGGCCGGACCATGACGCTCGGAAGCGTCAACCTCGTGCACAACGGATTCTCTCAGCGCGGCCAATTCAGTCCGGCGCGTGCCAATCTCTACAAGGGAAACGGCCGGGTCCGGCACGAGAGCCACATCGTTCAGCAGGGCCCCTTCCAAGCGATCCATTACCACTCGCTGCAGACGCTGGGCGACGGGGGCACCGAAGCCGGCGGCCCCCACGGAGTCGGCGAGCAGGGGCACATAGAGGTCCATGTATTCCGCAACAGCAGCTTCCACATGGGCTGGAAGAAGCATGAGACGCTTGACTACGACGCCCTCACCACAGTCTCGGAGTCCGGCGCCGAGGAACCCACACAGTCGGCCTCTCGCCGCCGGTCAATGCAGGAGTTCCTGGAGTACGTCAACGGCCGCCGAGCCAGGCGGGAGATGTCCTCCGAGCTCACCGACCACCGGCGCGGCGCCACTCTCATGGCCGGAACGTACCTCTCGGCAGCCCAGCAGTGGGTCGATGGATCGCCGGTGGCCAGGCTCGACTTCCGGCCGCACGGCGAAGGCGCCGCAGGCGCCGACCACCGTCTGGACGACCCGAGCTCCTGCGACCTGATGGACGTGTCCTTGTGACCCGGGCCAGCGAACAGATCCCCGTGGACACTTTGCCCGACCCCGAGAGGCTGCTCGGCGACGCCCTGCCCGACATACTCGCCGACTGCCATGACTGGATCGGGCGCATCGACGCGATCACGCGGCTAGAAGGCGGCAACGTCAGCCATGTGTTCCGTGTCGAGGGGACGCGCGGCAGCGTTGTACTGAAAGTGCGTTCGGCCACGTTCGTGCGCATCCCGTCCATGCGTACCGACCCGGCCCTCATCGGTGACGAGCGACGGGCCCTCGAGGTGTACGGCGCGCTGGCGCCCTCGATGTTCCCGCGGGTCCTGGCGTTCCACCCGCAGGCGCACGCAATGATCATGACCGATGTGTTCCCCGATCGGCGCAGTTACGAGGATCATCTCCAAGAGCGTGCCGGCACCTCGGAGGAACTCGCTCGTCTCGGCACGGCGGTGCGCTACGTCCACGAGGCGACGAAGGACGTACAGGTCCCCATCCGCTCCCAGGGCGACCTGTGGTTCCGGGAACACACCTTCAACTACAGCCTGCGGGCGAGCGGACACCCCGTGCTGGAGCGGGTCTGCCAAGAATTGAGCGCCGAGGAGCCACAGCGGCTCGTACTGGGAGACTTGGCCCCGAAGAACCTCAGTCTGGCGGACGGCCGGGTCGCGTTTTGCGATCTCGACAACGTGCACCGCAGCCGACCGGTCTTCGATGTGGGTTATCTGCTGGCGCACATCCTGCTGCACCACATCGACCAGCCGGAGCACCTTCCTGCGCTCCTGTCCGCGCTGCTCGACGCCTACTACGCCGACCGGCCGCCCAGCCTCCGCACGCTGCAACTGGTGGCGACGGTGGCGGCCGGCGTGATCTTCTACCGTCTCGACAACTCCATGGTTCCCTACCGCCTGGGAACCTCGGCACTGCGGCGCCAGCAGGTCCGCCGCAGCGTGGCGCGCCTACTGGACCGCGGACCCATCACACCGGACAGCCTGCATGACGCAGTGGCGGGTGCGCCATGAACCGTGCCGATCCCCGGCCCCTGCATGACGAGGACCGACATGCGCTCGCAGCCTTGCGCGCCCACGGATACCAGGTCCACGACATCCAAGACATCGCCCATGATCAGCGGTCATTCGCTGTGCGTGTGCCGTCCCGGCGGCGGCTCCTCGCCCCCGGAGTACGCTTCGCGTCCGAGACGGTGGAGCTCGGCGACGGAGCGTTCACCAATGCCCACACCCTCAGGCTCAACCTGGATCACATCAACGTCGAAGCGGTCACGACCACGGAGGGGTTCCACCTACGCGACCAGTGCACGGCGGACGGTGTGGTCGCGGCCGTGAACGGCTCCTTCTCCTACATCTCGGACGACCCTGCCCATCAGCCGGCTGAACCGTGCCTCGACTTCTGCTGCCGCGCGGGAACGACAGTGAGCCTGCCGACCGTGACCAAGCCCGCGTTCCTGGTACACGGCGACCGACTAATGGTGCGAACGCTGCCCGCGACCGGGACCCTGCGCATTGGCGACCGCTTGTTCGAATGGATCGGCTCCAAGGAGCCCCGGGCGTCGGCCGACCTCGCCGACGGCGCGCTGGTTGTCTTCGGCGCTGCCAACTGCCGGATCAGGTACGCCGACCACCCACGGACCGGCTTCGTCCGCTTCGTGCGCCCCGAGGAGAACATCACCCCGAAGGCTAGGTCGGTCGTCGACGCAGTCGTGTCACGTACCACGGCTGGCAGTCACGTGATCAGCAGCGTCCACCCTGGTGGGGGAGCAGAGCTCTTCACCGGAAGCTTCATACTCCGGGCTGACGCGGCGCATGCGCGGGAGTTGCGTTCGGGCGCCCGTGTGGAGCTGTGCACGATTGCCGGGCTCGCGGCCGACCTGCTCACTAACGGTGTCTCGCTGGGGCCGAGCGTCGCCGACGCGGCGACCGGCGCGGTCCCCGCGTACGACGAGTCCCTGGGAGTCTCACCGTTCCGCGACGTGCGGTACGCCCGCACGCTCGTGTGGACGACCAGACGGGAGATCGTCTTCCGGGTTTTCGACGGCGCGCCGCTGACCGATTCCTTCCGCGGTGTCTCGCCCACCGAAGTGGCCGACCTGTTGGGCCGGGAGGGAGTCGATCTGCGCGATGCCTACCACCTGGACGGAGGCCAGTCCTCGAAGATCGTATTCCGGGAGGGAGGACGTACCGGGGTCGTGGGAAACCTGCACTACCTCAAGTGGCCGCAGGAACCCGAAACGGAGTTCCGCTGGCGTGGCGTCGAGGGGCGACTCCTCAACAGTTGCTTCGTACTCCGTCTCCGTCGCGAGGCCGAAGGGCGCACTGACGCCGACACAGCGGCGGCAGACGTTAGCTGCCCCGGTATCGATAACGGGAGGGGGGGCAGTGGCTGAAGCCCATGGTACGCAGATCGGCGCATTGGGATCCGCGTCTCTGGTCCCGCATGCGGAGCCGTTCCGAGACGTCCTGAGCTGTCTCGCCAGCGGGGTGGTCGCCGTGACGGCCCGAGACACCGACGGCCGCCCCATCGGGCTCACCGTCTCCTCGTTCGTTTCCGTGTCCCTGGAGCCACCGCTGGTGCTCTTCTGTGTCGCGGTCACCAGTCGCACCTGGCCACGGATGCGTACGACTGACGGCATCTGCATCAACATCCTGAGTGAGGATCAACAGGGTGTTTCCGTGCGCCTCGCCACCAGTGGCACGGAGAAGTTCGACGACGTCGCCTGGACACCCTCTGCCAGCGGGATGCCCGTACTGCATGGCGCGTTGACCTGGCTGGAGTGCACCGTGACGGATGAGCACCCGGCCGGGGACCACCACATCGTGGTCTCCCGAGTCGACCAAGTCGCACCGGCCTCAGCGGGTGGCCCGCTCATTCGTCACCGTGGGCGCTATGTACGGCTGGCGAGCCCAGGCGCACCCAAGGATGCCTGCCAGTGACAACCAACAGAGAGATCCGGCGACGGGGCCTGAAGGGACGGCCACTGAAAAGCTACTCCACAGCGAGGGAATTCTGAGCCATGACAGCACCTCATGGGCAGCCAGCAGGCACCCTCCATATCGCCGCACATCAGCCCGGATATCATCGACACTTGTATTATTTCTACAAGATGGCGGTCAGCGACATATTCATATCGCTCGACAACGTGCAATATGTCGCACGCGAGTGGCAGAACCGGCAGGAGTTCTTCTATCGGGGTCGACGACGCTGGCTGTCGGTTCCGGTTTCCCGCGGTCGGGAGCCGATCCAAAGCAAGAAAATAACCGACCAGCATGCTCTGCGCAGCCACTGGTCCATCATCAATTCCGCCTACAATGATACGCCATACTTCTCAACCTACGCTCCTCTCCTAGAGGAAATCTACACTGCTGACTGGGAATACCTACGAGACCTATGCGATGCCCTGACCCACATCGTCCGTGAAGCGTTAGGTATCACCACCCCGTATCTGCGCGCCTCCGACCTGACGCCCCGGCCTTTACTCGCCCGGGGAGCTTTGCTGGCCGACTTGATTCACAAAGCAGTGCCGCTCGTACGGGGCTCAGCCCCCGTGGGACACAGAGAGGTTACCTATCTTGCTTGTGCGGCACCGATGCGTGCCGATCATTATCTCCTCCAGCCTGCTGCGGCATCATCAGCAGGCATGACAGAGCGCCAGGTCATAGAAGAGCAGGGCGTGTGTGTCGACTGCTTCGCCTACCGCCACCCGGTCTACCGGCAGCACCAGCTTCCAACGGGGCACCCCTTCGAGGCCGAGCTGTCCGCCTTCGATCTGCTGTTTAACCACGGCCCACGTGCACGCGGCATTCTGCTCAGCGCTGGTGGGCTGGCCCGCCAGGATCGCATGGGAGCCGAGATATGAAGAATGTGCTCATTGTCGTTGCGCACCCAGACGACGCCGAGATCGGCATGGGCATGCGCATCGCTTGGTACGCGCGCAACGGAGCTCGCGTACGCGTCCACTGCTTGACCACGGGCACGCCGGAGCAGGACGGTGCGCAACCTCGTAGGCAAGAGTGCCTCAGTGCTGGCCTCCTACTGGGAGTGGACCGTTACACATTCTCGGAGATTCCCGACACGCGTTTCACGGAACACCGCGGAAGCATCAACGCCGAACTTTTCGCGATCATCAGAGAAGCAGTCCCAGACGTGGTCTACACCCACTTTCCGGGCGACCAGCATATCGACCACGCCATCACGAGTCAGGAAGTCACGGCAGTAGCACTGCGGGAAGCTATGAACCTGTGCTATTTTCGATCACCCTACAGTACAGGATTTGAACCGAACCTATTTTTCATGGGCACCCACAGCCTCATGGAAGCGAAGATGCAGGCCCTCAGCTGCTTTTCCTCGCAAAAGCAGCTTGACATGGAAGTATTCCGCAGGATCGCCTCGGTCGCCCACCGGCAGCACGTGCATCACCGGATCGTCGAACGTTTCGCACCGGAACTGGAATACGTCGAAATGTTCCAAAGCGCGCGGCGCATCGAGTCAGCGATAGAGGCTCCCTCGATGGAGGGATAATCCGGAAGGAAGCGTCCGCGACAACCGCTGGGCGACCCCCGTCGTCCTCAGAATTCAGGAACGTGACACGTTCCGGATCATCATCGGCCCGGCAGTTGTCGCCCCGCTGGTCGCGGTGCTCCGCCATCTCCTCACCCCTTTCTCAACTACCTGCAACCGACCACGCGGCTGTCCGCACCGTCCGGGCATTACGCTTACAACGGCTAACACAATGAGCCGAGTTGTCGGTGGGTGATCAGGCAGCAGGCGAGTTTGAGGAACGCTTCGTGGATGTCAGCCCGTCGTTCCCAGCGGATCCGCAGTCGTCGGAAGCCGTGCAGCCAGGCGAAGCTGCGCTCAATCACCCACCGGTAGGTACCCAGCCCGGTGCCATGTCGCGTGCCGCGCCGGGCGATCGCGGGCAGGATGCCTCGGTCGCGGACCCGGTCGCGGTAGATGTCGTGGTCGTAGCCCCGGTCGGCGAACAGGGCGTCGGGCTTGCGGCGCGGACGGCCCACCCGGCCGCGGACCGGCGGAATCGCATCGAGCAGGGGCAGCAGCTGGGTGACATCGTTGCGGTTGCCCCCGGTCAACAGGACCGCGAGGGGTGTGCCATGCCCGTCGGTGATCAGGTGGTGCTTCGAGCCGGCCCGCCCGCGGTCGACCGGCGAAGGGCCCGTGTGCTGCCCCCTTTTAGGGCCCTGACGTGGGAGGAGTCGATCACGCAGCGGGACCAGTCCAGTCGCGATGCCGCGTTCAGCTCTGCGAGCAGAACTTCGTGGAGTCGCTGCCAGACGCCGGCCTCGTTCCAGTCCCGCAGCCGCCGCCAGCAGGTCATGCCCGAGCCGAAGCCCAGCTCCCTGGGCAGGTACTCCCACTGGATGCCGGTGTGCAGCACGTACAAGATCCCGCACAGCACCTCCCGGTCCGGCAGCGGCTTGCGACCCGGGTACCGAAAGCGCCGCTCACGCTGCGGAAGCAGCGGCTCCAAGCGGTCCCACAGCTCATCCGACACGATCCACGGTGATGTCCCCACAACGAGGGGAACGCTCAACTCCTGCCCTGGACACGGCAAGCAGCAGTGATCCGCCTCATTGTGTTAGCCGTTGTTAGCCAGCGCTGCGAGAGCACCCCGCGCCGCCGCGGCTACCCTCGCTTTGTCTGCGAGCAGGGCCGTGGCAGCGCGGGGCGCTGGTAGCGGACCTCCGTGCGGGCAAGGCTGCAGTCTTTCACCTGCATGACCCCTAGGTGTTCTGTCCGGGGAGGTTGTGGACGGGTGAGTCAGGTCTCGGCTGAGGGATCTTGAACGGGTGAGGGCCTTCCGGTTCGGTGTGGATTGCGACGTCTACACCAACAGAAAGGCCCTCGTGGTCCACCGTAATGCACCCCTGACCGAGACCGGCCGCCTGCGTCTGGCCCGCTGCGTCGTCGAGGACGGCTGGCCGCTGCGCCGGGCCGCCGAACGCTTCCAGGTCTCGCCGACCACCGCCCAGCGGTGGGCCGATCGCTACCGCCGGCTCGGCGAGGCAGGGATGACCGACCGCTCCAGCCGCCCCCACCACAGCCCGCGCCGCACCCCAACCCACACCGAGCGCCGCATCATCAAGGTCCGGGTCCTGCGCCGGTGGGGACCGGCCCGCATCGCGCACCTGCTACGGCTGGTGCCCTCCACCGTGCACCGCGTCCTGACCCGTTACGGACTGGCCCGCCTCGCCCATCTGGACCGGGCGACGGGCCGTGCCATCCGCCGCTACGAACGAGACCGGCCCGGCGAACTCGTCCACGTCGACATCAAGAAGCTCGGCAACATCCCCAACGGCGGCGGCCACAAAGTCCTCGGCCGGGCTGCGGGGCGCAAGAACCGGACGAACGCCGGCTACAGCTACCTGCACACCGCCGTCGACGACCACTCCCGCCTGGCCTACAGCGAGATACACACCGACGAGAAGAAGGAAACCGCCACCGCCTTCTGGAAGCGGGCACACGCCTACTTCACCGAGTGCGGGATCACCGTGGAACGAGTACTGACCGACAACGGCTCCTGCTACCGCTCACGCGGCTGGCGCGACGCCCTGGCAGCAGCCGGGATCACCCACAAGCGAACCCGACCCTACCGGCCCCAGACCAACGGCAAGGTCGAACGCTTCAACCGCACCCTGCTGGACGAGTGGGCCTACGCACGGCCCTACCGGTCAGAGACCGAACGCCGCGAAGCGTTCCCACAGTGGCTGCACTCCTACAATCACCACCGCGGACACACCGCGCTGAAAGGGCAACCACCCGCCAGCCGCGTCCCCAACCTCACAGGGCAATACACCTAGGGCGCCGTTCCCGCTCTGCTTGATGGCAGCCTGCGGACGTTACCGACGGCTGCGGCCTGTTCCCGCAGGCGCTCGATTTCCAGGTGCTGGGCGGCAATTTGAGAGAGGGTGCGTCGCTTGAAGTCCTTGAGCGCTTCCAGCTCGGCATCGCGTTGATCCAGCCGGGACTTGAGTGCGGCGTTGGCTTCCTTGAGCCGCTCGATCTGCGCGGCCCGAGGGTCAGGGATCGTCCCGGTGCCCCGCAGGGCGGCCAAGCGCCGCTCGAACTCCTGGGCCAAGTGCTGATACGGCCCTGGCCGGGCGGTGCCGTCGCGGTTCTTCTTGGCGTAGAAGGCGGTGCGGGGCACCCCGGCCTCACTCGCCAGCGTCCGCAGATCACACTTGCCACCAGGCGGCAGGTCGCCACGCAGCAAACGATCCATCGCCGCGCGGATCGACTCCTCGTTGCGGGCTCGGGTGTCCTCGCTGATACGTCCCATGTCACGCTACCGTTCCGGTCGCGGCGTCGATCTCGGCCAACACCCGCAGGTCGCGGTCGAGTTCCTTCTGCAGGCGGGTCTTCTCGTCCTTCTGCCCGCGTCCGATCTTGCCGATGAACACCTTCTTGTTCTCCGCGCTGGAGGCCCATACCGGCCGGTGTCGGCTGTGGTGGGTGGCCTGCGGGCAGCGGGCCGAGTCGCACATGCCGACCAGTGGTTTGTCCGCGTTCGGTGTGCCGGCCAGGAGCAGGCACAGTGCTCTGGAGGGGTCGGCGAACCAGCAGTAGTTCGCGATACCCAGGTGCAGGGTCTTCGCCCGGCGGGCCAGCAGTTGGATCACCTCCTCGTCCCCGGGGCGGATGCCAGGAAACGATGCCTGCAGTTCGCGGAGCTTGTCGTCCACGGATTCGAAGTGGGCGATCAGGTCGCGGGCGCCCGGACCGGCGGGGCGGATTCCGTTCTGGAAGTCGCGGAACGCCGCCAGTGTCAAATCCTTGCTGCGGATCTGCTCTTCCGCGCTGACCTCGGCCATGAACTTGGCCTGGGAGCCGCCTGGGCTGGCTGATGGTGGAGTCGGGTATTGGAACTCTCCGAATGCCTCAGTCGGGACGGTGCGAAGCGGGACGCCGGTACCTGGAGGGCACCCGGACTGGTCGACTGACGCGGTCAAGTAGTGGCACGCCTTCGTACCCCGCCGCGACGCCTGGTCCACCACGTACGCCGAGGTGGACCAGGTCCGGCTGACGGGAGCCATGCGCCGCTTAAACTCGACCAACCTGTCGATCACATCGTTGATCAACAGGTGGAACACCCAGTGACCTGCGAGATTCACGTCTACCGGTGCGCAGAAGGAGCCGGCCGTACCGGCAGTCCCCGGTTATGTGAACTGTCAAGCTGTCGCAGAAGGTCGGCTGTCGCAGGTCGCCGAAGCAATGGGCGACACGAGGTCAGCTATTCGCGTATGGTTTACCTCATGGCAACTAATATCAGGCCGTTCCGTCGTATCGGCGGAGTTTCGGAAGTGGCGGCGGAACTCGGAGTCAGTCGGCAGCAGGTCGCCAAGCTCCGTCAGAACGGTGACTTCCCGGCCCCCGTGGCGTCCCTCAGCGCTGGCGACATCTGGGATCTGGACATCATCCGGCGGTGGGGAAGCAGTGGTCTGAGGCGGGGAGCGGGGCGACCCGCGCCCGTTGGGCAGCCTCGTTCGGTCGGGCGCCGATTTGAACTCGGGGCAGAGATCGATGGCGGCGGGTTCGCAGTCGTGTTTGGCGCGCGAGACCTTGAGGCGGCCGACGACGATCGGGTGGCCGTAAAGGTCCTGCAGCAGACGCATGCACTCGACGTGGAGACTGTCGCCCGGTTTGAGCGGGAACTCCGTCTGATGTCCACGCTCGGCCATGCAAACGTCATGACGCTGCTGGCGAGCGGGAAAGATGAAGATCTGGGTCTGTGGTATGCAATGCCGCTCGCCCGAGGTGTCCTTTCCGACGAAGTCGGTAGCGTCATGAAGGCCGATGACGTGGCTGCCGTGATGCGAGACATCTGCGCCGGACTTGCATATATTCACAGTCAAGGGATTCTTCATCGCGATCTCAAGCCGGGGAACGTGCTGCGAACCCCTGACGGGGTTTGGGCCATTGCCGATTTCGGGCTCGCGCGAGTAGTGGAGGAGAGTGGTCTGCTCACCTCCACTTTCGATGGCATGGGAACCCGATTTTATGTTGCCCCTGAGCAGTGGAGGGACGCCAAGCATGTTGACGAGCGTGCGGACATCTATTCCGCAGGCAAGATCATGCAGGCTCTCCTGACGGGCGCCACTCCGGTGGACGACGACGTGCCGGCCGGACCGTTGCGTGCCGTGGTCCAGCGTGCGATCTCCCAAGATCGCAGTCGGCGCCATGCCAGTGCGACCGAGTTGCTGGCGGCCATCGAAGCGGCAGTCGCCCCGGCCCCGACCGGGAAGTGGGAAACCGCCGAGGAGAAGGCGGGACGCTTGCGCCCCCGTCTCAAGGCCGGCCGTGTCGTGGATGAAGCTGCGCTCGACGAGTTCGTCCGCTGGGCAGACGAGCTGGACTTCAGCGATTACGAAGACATGGGGGAATTCGCCTGGACGCTTAGCGCCCTGCCGTCGGATTCCGTGGAGTGGTGGTGGAAGGAGAATCCCGCAGGGTTCACCGGAATCTTCCAGGCGTTCACGAATCGCCTGGAAGGGTCCTTCGATTTCGGAATGTGTGACGTCCTCGCCGAGTTCGCTCGCCGTGCCGTCACGGTCACGGGCGATGCGATCATTCTGCGTGAGGCCGTCCGTGGGCTTTCCCATCTGGGCATTAATCACAACCGCTGGCATGTCCGTGATGTTGCCGTTGCTATTCTGCAGCAGGTCCGAACACCCGAGGACGCGGTGGCCGCTCTCGAAGGACTTCGCATGGCAGGAAAACCTGCCGCCGAATGGACGGTGGGCAGCACGGTAATTCGAACCCTGCATCCCGTGCTGCGAAGCGGTCTCGGTACTTTCATCGAATCTGACGACTGACGACTGGCTGCCGACGGGCCGTGGGCCCGTCGGCAGGGCGGGCGCGAGCATGTATTCGACTATCTCGGGCGGATCGGGCTGACCCCGGCCGCTGCTTCGATCCGCCCCGTCAGTCGCCGGTTCTCCTCCTGCAGCTCTTCGTTGCGGAGAGCCAGGACCTGTATCTGGTTCGCGTAGATCTTGTTGGTCTCTTCCAGGTCACGGATCGCCTCGGCTTGCTTGCGGCTGAATGCCCCGCCCGTGGAGCCGCGAGTCTGATCGTCGGTGACTCCGTGGGGCTGGCTTCGGTTGGCAGGCTGCTGGTTGCCAGCGCTGCTCTCATCGAGTACGAATGCCGTGGTGGAGGGGCATCGGAGCACATGGCGGAGACGCATCGATAGGCGCTCCTTTCCAACAGTGCGCTAGCGGAGATACTCAGAGGGAATGCAGGAAAGCGGCGTCGCGTGGACCTCATCCATGCGGGGAAGTCCCGCGTGGAAGTCCATTTCTCCGGGCCTGAAGTTGAACAGCACGCCGACAACTTTTCCAGTCTCGACATCCGTTACCGCGGCACCGCTGAAGCCGCGTGGAGGGATGGCACCTGCCAGTACGATGAGAGACTCCTCGACCGGGCCTTGGACCGTGTAGTCCTGCACGGCTCGCAGTCCTCTGTCGCGATTTTCCTTATCGCGTCGTCCCTCTGTCCAGCCGGTAACCTTAACCCTGGATCCGGGGCTAGGGAGATCGGCCGAAACGCGGGACAGCCAGGGCCAGTCCCGATCGACAGTCAACACCGCCAAGTCGAGGTCCTCATCGCGATAAATCACGCGCGCCTGGATCCAGGTGTCCCCGAGCTTCAGCTCCGTGCCGGTCGCGGCAACCACGTGCGCCGCAGTGACCCAACGCCTCGGAGCGATCTGAACGGCGCTTCCGAGGCGGGCCCCAGCTCTTGCTTCTCGAGTCAAGATGCGTGCTACTGAATTATCCACCGACTTAACTCGCCACGGAATCAGCACCTCCTTCCTCACGACTTGTGAACCGCTAACTACGGCAGCGATAACCGCAGCGATAGCGACCCAGCTTTGCAGTCCAAGGATTGCCACCAGTGCGGAAACGATACTCACCAGAACCAAGGTAATGGCCGCCATACCTCCTTCGGTCATCTGGCGTGCTTTCTTTAGGCGATTCACGAATACACTCTCCCTATCCTTGGATTATGCGTACTTGAGTTTCTTGTAGCGGTTCAGGCATTGGAATTTCGAAAAAGGTTCTGCTCATGAGCTGGTACGGTGACTGACGTCGGCGGCGTAGGCGGCCCAGTCCCCTGCGGACGCTTGCTGCCACTGGACGGCGACCTTGATGTGGACACCGAGCATTCGGGCGAGGATCGCGGCGGGGAGTTCGGCCGCGAGAGTGAATAGTGCGGTGGAGCGATCCTGTTTTGGTCGGATCCCGATCTTATGGAGACGGTTGCCGATCTGGCTGTCGGTGAGGGGGCGCCCTGGATGTCCTCCCGGGAACAGCCAGGAAACGTCTTCCGGAGTACCGATCTTGGCCTTGCCGCGGCGGGTTGCGACGAGTTCGCGGACCAGGCTGGCCAACGGCGCGGGCAGGACGACCGGCGAGGTGCCGAACGTGATGGAGACGGTGTCGCTGTCGAAGTGGACGTCATCGACGGCGAGTTGGCTGATGGTGGCGATCTTCTGTGCGTAGAGGATCAGCAGTAGTCCCGCGACGCGGTCCGAGGTCGGCAGCGTGTCGTCGTTGAGGAAACGGCGGGCGTCGTCCCAGCGTTTCTCACTGTCGATGGTGCCGAGCGGACCGGTCCAGCGGACGGTGCCGTAGGTCAGATCGTGGGCGTGTCGGTGCTGTACCGACCAGCGGACGAAGTGGCCGGTCTCGTCGCGGTAGCTGACCGTGGAGTCGGCCATCCAGCGTTCCAGGTCCGTCTGGGTGCAGGTCCCCAGCGTGAGCCCTTCACCGGTGAGCCAGTCGAGGAAGTTGTTCGCCGCGGTGACGTGGCAGCGCACGTTCAGGTCCTGGAGCCGGGTGGCGTGCTCTTCGCCGAGGCGGCGCCGGAATCGGCGCAGGTGGTGCCAGACCGCGTAGCCGTGCAGGATCCGGCGCTCGGCGAGGTCGCTGCGGGTCTGGACCGTCGCAGTGATCCATTTCTCCAGGGCGATGAGGCGCTCCTCGCGGGATGGTAGGGCTCCGGTCGCGACCAGGACACTGCGCAGGTGGGCCAGCACCTTGCCCGGGGGTAGTTCGTCGAGGACCTCGTGGGTGACGGGCCGCTCATCGTGTCCTAAGCGTTCCAGGAGGTCACGGACCTGGGAGCGGGAGACCCAGGCGAAGGCGACGTCCGGGCGCTCGGAGCTCGTTAACGCCTCGTGGAAGGGCACGAGTTCGGGCCGGATTGCCCCGGTGGCGTCGCCGAGGAGGTCGCGTACTCGCTGATCGAGGACGCATCGCTGGCAGGGGCGGGTGCTGAGCTGCCAGGTGACGGTGCAGACCGGGCAGCGGCCCCAGAAGGTGGGGTCGGGGTTGGTGCACTTCGCGCACAACGGCGCCTCCCAGGTGCCGCTGCGGGCCTGGGCGACGGTGCCGCAGTTGCTGCAGGCCACCCATCGCTGCTGGCAGCGGTCGCACCAGGGCTGGCCGGTGGCCCGGGACATGTCGCAGGACGCCGTCCGCCCGCAGATGCCGCACTCCGCGATAATCCTCGGCCGGCAGTTCTGGCAGCGTGGGCCATCAGGCAGCCGGTTCGCGACGGGCTTGCGGCGGCGGCAGCCGACGCACTCCTCCAGATTCGCGGGCTGCCTGATCATGCAGTTCGGACACAGCGGTCGGCCCTCGGCGTCACGGGTGGCGGGCTCACGCACGGCGCCGCAGCCGAAGCAGGGGACGGCCGCGTGGCGGGCGAAGCAGGCCCGGCAGATCCTCTTGCCCTCCAGCAGTTTGGACAGCGCCTTCACTTCGTGGCAGCGCGGGCAGGCAGGCCGGACGATATTGGTCGCCCCGGCATCGACGAGCTCGTTGATAAACCGCAGGGCGGCCGGGGTGGGGGCTTCGTAACCGGCGCCGGTCAGCAGCTCGGGGCGGGCGACGACGGCCCAGGCCAGGCGGCGTTGCCCGGCGGGCCGGACGGTGGCGCGACCGAGTGCGGCCAGGACCGCGTCGGTGTCGAGGGCGGGATCGAAGCCCGTGATCAGCTCAGTGAGTTCCCGCAGGGGATCACCGTCGGTGTCAGGGCAGTTCGCGCAGCGCGGCTCGCCGTTGCGGTCCCGGCTGGTGACGCGTCGTTCTTCGTGACAGCCCGCGCAGACCGCCGGCTTGTCGAGGCAGGGTGAGCATCCCCACCGTCCTCCGGTGCTGCTGCCGACGTAGCGGCATGCGCGTCCACACTCGCCGCAGCAGGGCAGGGCGACGTTCTGGGCGCCAGCATCATGCAGGGCCATCAGCAGTTTGGCGACGCAGTAGGGCGCCGGCGGCTGTCCGGTCCGCAGCAGCGAGGGGTCATCGTGCAGGGCCTGGGCGAGGCTGCGGCGACCGGCTCGTGTACGTACGACTGCGAGGACAATGTCGCGGACGTGCTCGGCGGGCAGGTGCTTTTCGACGTTTCCGACCAGCCGCACGACCAGGCCGATGGGATCCGCGAGGACCTCCTCGGAAAGACCGGTCACCGGTCAACTCCACTGATCCGGGCCCGCCGAGGCCGCAGGTCACCGACTCCTTCGGAGACCGAAGAACCGCCTGCGGCAGCCTTCTTCGGCTTCGTCGCAGCGCCCGCCACGGCGATAGGCTCGATGAGGTCGTCCATGGTGCAGTCGAGGATGTCGAGCAAGGCCATGAGGATCTTCAGGCTGAGGCGTTCGGGACGCTCGACGACGAGCCGGTAGACCTGGCTCGAGGACAGGCTGATGCCGCGTTCCTTCAGCGGCGGGATGAGGTCGGTGGTGGAGAACATCCCGCGGTCCGCCATGACCTTGCGCAGGTGCCAGTGGTAGTCGAGCTTGGCGGCCATCATCGGGTCCTTCCTCGTCAGACGCCGGCGAACGCCGGGGCCAGGGCCTTGCTCAAGGCAGTGTTCATGAAGTCGTCGCTGACGTGCGTGTAGATGGCCGTGGAGCTGTCGCACTCGTGACCGACCTGCTGCTGAATGAAGCGCCGGTCCACCCCGTCCTCGGTCAGATGCGTGACGTAAGAATGACGAATTGAGTGCGGAACTAGTTCTTTTGGGAGATTCAGTGCGTCCCGGTATGCCTCGAACCGGTCGTTGATCGAACTCGGCTGCAGGCGTCCCCCGCGTTCGGTGATCCACAGAGCCGGGTGATCGGGGAAACCGAAGCGGGGCCGGACGTTTTCGACGTAGTCCTCGACCGCCTCGACAGCCCAGTCCATCACCGACAGCACATTCCTCCGTCGCGGGGGCTGGCCCTTCTTCGCCTTGCCGTAGCGGACGTTGAGCGTGCCGTACCGGCCGAACTGGCGAGCTTTCGGGTTCCGTCCGAAGTCGACCACGTCCAGCTTCGACGTCTCGGTCCGGCGAAGGCCCCAGCCGTAGATGACCTTGAAGAGGGTGGCGTCCCGGTAGGCCGCGAGAGCACCCTTGCGCTTGGACTTCACGGCCCGTGCGACCTGGTCATCGGCATAGTCGAGGAACCGCTGCAGTTCTTCGCGGGTGAACGGCCTCGCTTCCGGATCACCTTCGTAGTCCTGCAGGTGAGGGAGAGTGTTCCACTCGTGAGCGATCGCCACCGGGTGGACACCGAAGGCTTCCTCGCAGGCAGGTCCCCAGCCGTAGCGGCCGTCGATGAGGAACTCGGTGAACAGCCGGATGTCGCCCTGGTAGCTGCGGATCGTGGACGGCGCCAGATGCTTCTCGCCCGTCAGCGAGGCGGACCACTCGTCCATGTGGGCCGGTGTCCATTGCCACGGGTAGTCGTTCGCGAACTCAAGGAACCGGCGGACGAGCCGTTCCCTAGGGTCGATCGTCTCATCCTTCAACCCGCGCGACTTCTGCTGAGCCCTCCAGCCCCGCAGCATCGCGTCGAACATCGCGTCCTCCGGACGCAGCTGAACCACCCCGGACACGAGCTCCAGACGAGCCGCCCCGGCCAGGGCCACCTTCTGCTGATGAACCAC

Protein sequences of DBSCAN-SWA_1

>NZ_LN831790|101352:142427|134287_134770_-|WP_029381463.1|DBSCAN-SWA
MGRISEDTRARNEESIRAAMDRLLRGDLPPGGKCDLRTLASEAGVPRTAFYAKKNRDGTARPGPYQHLAQEFERRLAALRGTGTIPDPRAAQIERLKEANAALKSRLDQRDAELEALKDFKRRTLSQIAAQHLEIERLREQAAAVGNVRRLPSSRAGTAP
>NZ_LN831790|101352:142427|132194_133045_-|WP_099053560.1|transposase|DBSCAN-SWA
MPCPGQELSVPLVVGTSPWIVSDELWDRLEPLLPQRERRFRYPGRKPLPDREVLCGILYVLHTGIQWEYLPRELGFGSGMTCWRRLRDWNEAGVWQRLHEVLLAELNAASRLDWSRCVIDSPRQGPKRGQHTGPSPVDRGRAGSKHHLITDGHGTPLAVLLTGGNRNDVTQLLPLLDAIPPVRGRVGRPRRKPDALFADRGYDHDIYRDRVRDRGILPAIARRGTRHGTGLGTYRWVIERSFAWLHGFRRLRIRWERRADIHEAFLKLACCLITHRQLGSLC
>NZ_LN831790|101352:142427|135743_137303_+|WP_029381465.1|DBSCAN-SWA
MATNIRPFRRIGGVSEVAAELGVSRQQVAKLRQNGDFPAPVASLSAGDIWDLDIIRRWGSSGLRRGAGRPAPVGQPRSVGRRFELGAEIDGGGFAVVFGARDLEAADDDRVAVKVLQQTHALDVETVARFERELRLMSTLGHANVMTLLASGKDEDLGLWYAMPLARGVLSDEVGSVMKADDVAAVMRDICAGLAYIHSQGILHRDLKPGNVLRTPDGVWAIADFGLARVVEESGLLTSTFDGMGTRFYVAPEQWRDAKHVDERADIYSAGKIMQALLTGATPVDDDVPAGPLRAVVQRAISQDRSRRHASATELLAAIEAAVAPAPTGKWETAEEKAGRLRPRLKAGRVVDEAALDEFVRWADELDFSDYEDMGEFAWTLSALPSDSVEWWWKENPAGFTGIFQAFTNRLEGSFDFGMCDVLAEFARRAVTVTGDAIILREAVRGLSHLGINHNRWHVRDVAVAILQQVRTPEDAVAALEGLRMAGKPAAEWTVGSTVIRTLHPVLRSGLGTFIESDD
>NZ_LN831790|101352:142427|118421_119216_+|WP_049976675.1|DBSCAN-SWA
MREDLPGYAGKVALVVGSSRGLGRQVAELMADQGARVIVNSASTTVDGKNVARTITKNGGQAHYVCADVASEDQVAAMASLIQEKFGRLDIVVHCAAGGSEARVMDATFPMFERTFRVNSYSLVTLARHLSPLMPAGSRFVYMSSMGAIRASHGYGVVGAAKAASEALVRSLALELAPLNITVNGVRTTAFPSLSLRYFSKGGDWLDICERESPLGPPQAGKIAEAILLLCSQAAGYITGQVLNVDGGWLTSVLRTRGAEADVS
>NZ_LN831790|101352:142427|134771_135302_-|WP_029381464.1|DBSCAN-SWA
MAEVSAEEQIRSKDLTLAAFRDFQNGIRPAGPGARDLIAHFESVDDKLRELQASFPGIRPGDEEVIQLLARRAKTLHLGIANYCWFADPSRALCLLLAGTPNADKPLVGMCDSARCPQATHHSRHRPVWASSAENKKVFIGKIGRGQKDEKTRLQKELDRDLRVLAEIDAATGTVA
>NZ_LN831790|101352:142427|107401_108646_-|WP_164497180.1|DBSCAN-SWA
MTGHQMSAGELADAVNDAILQLTGRAGATSERTVFRWLSGENQWPQDRQRRALEMVTGLSPTALGFVPRGRHKTVPPALPEDPDVRRRQFCSAATGAAAAAVMPAPAPRSRVGTSDVLRLRDDVEKLVALDAARGGHGSLAHAALAGADEALGLQSKSATQRVRQRLYALASDFTATAAWALIDAGQLDGAGKHLDRALTLAGLAQDTEMAMQVWNLRAMLARQRKRYPEAVAAAQAAQATPIVRRSPLHASLAQARMAVGLAHSGDRSAALRCLGRAEDALAKTDPAQPRSTWIAFYSWAELHSLTAIVRDVVGDPAEAEAAAHRALAALPDTYRRNRAHTTARLALAQLHQDDIEQACATSGTVFAIMAGAPLPGRMRQLLGDFQRDLIARAPSAHIAHEWTDHYRTEWSTP
>NZ_LN831790|101352:142427|133337_134291_+|WP_047122297.1|transposase|DBSCAN-SWA
MVHRNAPLTETGRLRLARCVVEDGWPLRRAAERFQVSPTTAQRWADRYRRLGEAGMTDRSSRPHHSPRRTPTHTERRIIKVRVLRRWGPARIAHLLRLVPSTVHRVLTRYGLARLAHLDRATGRAIRRYERDRPGELVHVDIKKLGNIPNGGGHKVLGRAAGRKNRTNAGYSYLHTAVDDHSRLAYSEIHTDEKKETATAFWKRAHAYFTECGITVERVLTDNGSCYRSRGWRDALAAAGITHKRTRPYRPQTNGKVERFNRTLLDEWAYARPYRSETERREAFPQWLHSYNHHRGHTALKGQPPASRVPNLTGQYT
>NZ_LN831790|101352:142427|105011_105248_+|WP_157840680.1|DBSCAN-SWA
MAFYKDGEELIPMHDKEERVSRELSAVAAGFTVNNAALINGGIAAGKEKLRRRRIVIAVCSVAIALLGIAVMAGVDLY
>NZ_LN831790|101352:142427|110272_110941_+|WP_029383693.1|DBSCAN-SWA
MSIILMSDPRVAAIPVADCGEPLVDVRESLLVDDRKADAADAFVHIRQGVLDRLLHAQSLLPGGLRLLFIEGYRPPHLQRRYFEQYADELRTANPAWTQEQVHEAASRFVSPPEIAPHSAGAAVDLTLVDADGRELDMGTRVNASPEESDGACYTDAPGLSGRARTNRTTLGSALSSAGLINYCTEWWHWSLGDRYWALQTGQPAALYGPVDLPQKPRVSGR
>NZ_LN831790|101352:142427|130558_131329_+|WP_157840618.1|DBSCAN-SWA
MYYFYKMAVSDIFISLDNVQYVAREWQNRQEFFYRGRRRWLSVPVSRGREPIQSKKITDQHALRSHWSIINSAYNDTPYFSTYAPLLEEIYTADWEYLRDLCDALTHIVREALGITTPYLRASDLTPRPLLARGALLADLIHKAVPLVRGSAPVGHREVTYLACAAPMRADHYLLQPAAASSAGMTERQVIEEQGVCVDCFAYRHPVYRQHQLPTGHPFEAELSAFDLLFNHGPRARGILLSAGGLARQDRMGAEI
>NZ_LN831790|101352:142427|116862_117624_+|WP_047121428.1|DBSCAN-SWA
MRTQTERPGLAAQFVDLWLMQLSNWRWSWRAMMVTGIITPLMTVAALGAFAKGRGHESLVYVLTGSILLSLMFENQNKVAQNFAYMKAMGTLDFLGTLPVRRQMVITATVLAFFALSAPALLTTLMLGSLILGVHLSVSWLVVLVIPLCVLSLAGIGAVIGIVTRSQEEASSLTLLVTMLLLFFGPVIIPASRLPGWLVTISHVSPTTYAASAIRQVLVGPVTGRIWLDLFVLLALTGITLWFAGSRMQWKAN
>NZ_LN831790|101352:142427|137362_137677_-|WP_029381466.1|DBSCAN-SWA
MRLRHVLRCPSTTAFVLDESSAGNQQPANRSQPHGVTDDQTRGSTGGAFSRKQAEAIRDLEETNKIYANQIQVLALRNEELQEENRRLTGRIEAAAGVSPIRPR
>NZ_LN831790|101352:142427|127469_128480_+|WP_029381184.1|DBSCAN-SWA
MTRASEQIPVDTLPDPERLLGDALPDILADCHDWIGRIDAITRLEGGNVSHVFRVEGTRGSVVLKVRSATFVRIPSMRTDPALIGDERRALEVYGALAPSMFPRVLAFHPQAHAMIMTDVFPDRRSYEDHLQERAGTSEELARLGTAVRYVHEATKDVQVPIRSQGDLWFREHTFNYSLRASGHPVLERVCQELSAEEPQRLVLGDLAPKNLSLADGRVAFCDLDNVHRSRPVFDVGYLLAHILLHHIDQPEHLPALLSALLDAYYADRPPSLRTLQLVATVAAGVIFYRLDNSMVPYRLGTSALRRQQVRRSVARLLDRGPITPDSLHDAVAGAP
>NZ_LN831790|101352:142427|125928_127473_+|WP_049976676.1|DBSCAN-SWA
MKNFLVIGVGPHARLNHLPSLWAGQSAGLVGRVIGVDVADAVGDIAASNSAGGTPELSVTFIEPFDATRRTLPAPVRKTLDSLVREHAVDAVVISTEPSFHMVYTHWALGHGLSVLLDKPLSVHANCSVDPFKASAILTDFDEILARYEAVRRTHPEVLVTVQCQRRYHPAFRHMRRLIAEVAEATNCPVTSVQSFHSDGQWRMPNELIDISYHSFDQGYGKCAHSGYHFFDIVPWLLRAGEAPGKELDSVDIHANFSRPRDFLAQLDVNDYARLFPEFEAANPYTQAHLLTATEAFGEIDAFVSMAYKSGGRTMTLGSVNLVHNGFSQRGQFSPARANLYKGNGRVRHESHIVQQGPFQAIHYHSLQTLGDGGTEAGGPHGVGEQGHIEVHVFRNSSFHMGWKKHETLDYDALTTVSESGAEEPTQSASRRRSMQEFLEYVNGRRARREMSSELTDHRRGATLMAGTYLSAAQQWVDGSPVARLDFRPHGEGAAGADHRLDDPSSCDLMDVSL
>NZ_LN831790|101352:142427|113209_114313_+|WP_047122292.1|DBSCAN-SWA
MTAGSIAKFHWFLPTASDGRSLAVGTHGTHGAAAGGDQAPEGGADRFRAPDIAYLAQVARAAEQQGFDGILTPTGTWCEDAWLVTAALARESERLKFLVAFRPGSVSPTLAAQMASTLQRLSRGRLLLNVVTGGERDEQARFGDHLNKDQRYARTGEFLTVLRGAWSCTPFDFKGEYYDVRGATVAAPPNPLPEIYFGGSSEAAGPVAARHVDTYLTWGEPPAQVAEKLAWMRRLASEEGRALRFGIRFHVVARDTSREAWAAASRLLDRMDSAHVAQVQNVLAASESTGQARMRALHETFREGWRHDDLEIYPNVWAGVGLLRGGAGTALVGSHAEVADRIEEYRALGIEEFILSGFPHLEEAYNG
>NZ_LN831790|101352:142427|105372_105714_+|WP_029383688.1|DBSCAN-SWA
MTVLRELAEPEVGGFGWGYNGGGTSAAAAAILADALDLGDPDKCGIGYATYPEDEVLAQLREDFCDDVLSQLCDQWRVRRGVVLRWSLAWCLQRGIDELPAALRELPPLQSQS
>NZ_LN831790|101352:142427|129899_130406_+|WP_164497166.1|DBSCAN-SWA
MVPHAEPFRDVLSCLASGVVAVTARDTDGRPIGLTVSSFVSVSLEPPLVLFCVAVTSRTWPRMRTTDGICINILSEDQQGVSVRLATSGTEKFDDVAWTPSASGMPVLHGALTWLECTVTDEHPAGDHHIVVSRVDQVAPASAGGPLIRHRGRYVRLASPGAPKDACQ
>NZ_LN831790|101352:142427|102236_102536_-|WP_029383687.1|transposase|DBSCAN-SWA
MGSKYTKRYTEEFKRDAIALVDSSGKTVTAVARELGISSESLRGWYRWAKADRGEGGSGELTSAEREELKRLRKEVREQQQTIEILKKATAFFVKENDR
>NZ_LN831790|101352:142427|141323_142427_-|WP_029381470.1|integrase|DBSCAN-SWA
MVHQQKVALAGAARLELVSGVVQLRPEDAMFDAMLRGWRAQQKSRGLKDETIDPRERLVRRFLEFANDYPWQWTPAHMDEWSASLTGEKHLAPSTIRSYQGDIRLFTEFLIDGRYGWGPACEEAFGVHPVAIAHEWNTLPHLQDYEGDPEARPFTREELQRFLDYADDQVARAVKSKRKGALAAYRDATLFKVIYGWGLRRTETSKLDVVDFGRNPKARQFGRYGTLNVRYGKAKKGQPPRRRNVLSVMDWAVEAVEDYVENVRPRFGFPDHPALWITERGGRLQPSSINDRFEAYRDALNLPKELVPHSIRHSYVTHLTEDGVDRRFIQQQVGHECDSSTAIYTHVSDDFMNTALSKALAPAFAGV
>NZ_LN831790|101352:142427|106871_107417_-|WP_047121425.1|DBSCAN-SWA
MEHPLTTTAVELRRFGHEDLQAIRQTLLDVHADAYADQMDEFNQRFPWFVDHWGEHPGFACVIGYDGDEPVGFAYGAPATPGREWWREHLSEPPANDSTFSVSELMVRPRWRKTGTAERLHTALLEDRPEALAVLLVDPDHPKVQALYEAWGYAKVGHRQPFPDSPNFAVMLRHLHLPTVS
>NZ_LN831790|101352:142427|109290_109527_+|WP_047121426.1|DBSCAN-SWA
MSTTHGLLHGDHRWIGREVEDTASGRRGILRAIAPEGGNPRPVAWLWPKGGGTEWTTDPAALANPAPLTPDDYRREER
>NZ_LN831790|101352:142427|119263_123430_+|WP_029381182.1|DBSCAN-SWA
MEFEPIAVVAAECRLPGAANLQEFFRNNQEGTCSISKALDAFWDGCEVYDKNDGGHLNTSYTDLGGFLDPWELDRGVFRIAPRVIERMDPAHALGLEMAHRVIEQAERSGPLPRDETAVVVANVGGGSTSRINANMKVQSERWAGALRRREPTLANVLDEHQNNERTRHPDKREDLALNGESGTIGGRIANYFNLRGTHYGIDAACGSSLAAVHSACMGLHQGEFDAALVTAVGILTPDIFVVNSAARTLSKDGSFPFGSAANGLVPGEGGVGLLLMRLADARQQGRPVLAVTRSIGYSTNGRTTSTWAPSAEAEERAIRRAFDGMPFGMEDVDYVEAHGTSTRAGDEAEFDALLRTYGSVTRSRPLPFGSVKSLIGHTVESAGLVGILRGLFIFETGTLPPTVNVDDIRPEVAGAADRLWLQRANEGLTPAPGRPRRVGVSAFGYGGINYHLLLEHPGTEAAAISRSNPPLRRDRTPIAIVGLEAVQPDATDAAAFWRNLQEGLASRQDLRGRVPSRDLDVEDAGLQRQATHLQNAAFVDVPGTVDNTRFRILPNQVPGLTDEYLVLLSCAANLASAVEHATAAIDPTRAGCIIGQLPDSDREFELMQSLRFMPWLRRLRRLARARGIEAPWSALRDDLWNDPTLELHTVNQDTSVAGFGSTLPSTLASSFDLRGKSYAVRAACATGLAALSLAVQELREHTLDFVLCGAVGMGVGLVNHTALASIRALSANGVGRPYDEKGDGFIMGGGAGLLCLKRLPDAERDGDPIFAVVREVRGGSDGKGRSLLAPNTEGRRFTMERTYRNSGLSPASITYVEGHGAATALGDRSEVEALSAVLGNEETVFLGSAKGNVGHQKGASGMTSVIKTVLCLHHGELVPTPGYENPHPALELEQRRFQVLTETRPWPAPRDGAPRRAAVNAFGLGGINYHAVLEEYLRPEPSRQSAARTTPRETSPEPTIAIWTAPGQEELDRSLAAFAEHGEAPPPPDSAHTHRVAVDGGTGPDAAKALHDKVRRYLATGPDTLTPAQWDAMGVFTGRTDLPTGGVCRLYPGQGSQYPGMLREAAPAIDGAEDKVRAAASALSAQLPGLLDDFWHADFATCEQWLSRTENCQVATLVVSAALGDWLDGLGVAADFHLGHSFGEVSALAAAGAIPLPDALRTAHRRGTIAAQGRGGPRQGMAVLFTSAAEATRFIGEDDNDVVVANRNSRRQVVLAGNAEALTRVLRRATTDGIEARALPIERAFHSPLLRDAIPAYRAFLDSVPVTSPPAPVYETLTSRPYPRNTEPGRIRQSLADQFVLPVYFETMVQDAYDRGARVFVEVGPKRALSSLVGECLGTSAKVRTVTLLHPKGGEVAQVRRAAAQLWAIGLTDVRPVSDVTARKAAT
>NZ_LN831790|101352:142427|112189_113182_+|WP_078648201.1|DBSCAN-SWA
MNVDIDHVRALMVEACRRSAVPAESVDLVVDHYLLGETQGKYSHGVAKFCFESQFFGERQGSPRTVRERGVLAIVDAQREIGPVSADHAVRIAADRARELGAGIVGMINTQRYGILSPWAEHLARAGFLGIVMNTSRADSTVEGARTPFLGVNPISYAVPTTGEPLVVDMSTTKSPMGVLWEARRGAAQLPAESFVDLDGDFTVDPHLAESAMVFGGHKGFAVSLLIQIMTGSLFGFPMGPGVESTWTTGYTFIAIDPSFGGELDDFPNNNARLVEVMEGVGTRDSQPFRIPGRRSRAHVRKVTALGKLDIPDSVYRRLRARAAGDFVSD
>NZ_LN831790|101352:142427|114337_115187_+|WP_099053558.1|transposase|DBSCAN-SWA
MPCPGQELSVPLVVGTSPWIVSDELWERLEPLLPQRERRFRYPGRKPLPDREVLCGILYVLHTGIQWEYLPRELGFGSGMTCWRRLRDWNEAGVWQRLHEVLLAELNAASRLDWSRCVIDSPRQGPKRGQHTGPSPVDRGRAGSKHHLITDGHGTPLAVLLTGGNRNDVTQLLPLLDAIPPVRGRVGRPRRKPDALFADRGYDHDIYRDRVRDRGILPAIARRGTRHGTGLGTYRWVIERSFAWLHGFRRLRIRWERRADIHEAFLKLACCLITHRQLGSLC
>NZ_LN831790|101352:142427|108946_109294_+|WP_047122291.1|DBSCAN-SWA
MLYVCAERGKLNPTLAEERAEEEGRALAQQHGLTITDTVRDEYGEPEPCLRVGWQRVRQLAQSGAAAVVITRWPTCIAPESSRELRYREIRWLQEHGVRVRYSWAPLAQSGGEAR
>NZ_LN831790|101352:142427|138556_140965_-|WP_029381468.1|DBSCAN-SWA
MTGLSEEVLADPIGLVVRLVGNVEKHLPAEHVRDIVLAVVRTRAGRRSLAQALHDDPSLLRTGQPPAPYCVAKLLMALHDAGAQNVALPCCGECGRACRYVGSSTGGRWGCSPCLDKPAVCAGCHEERRVTSRDRNGEPRCANCPDTDGDPLRELTELITGFDPALDTDAVLAALGRATVRPAGQRRLAWAVVARPELLTGAGYEAPTPAALRFINELVDAGATNIVRPACPRCHEVKALSKLLEGKRICRACFARHAAVPCFGCGAVREPATRDAEGRPLCPNCMIRQPANLEECVGCRRRKPVANRLPDGPRCQNCRPRIIAECGICGRTASCDMSRATGQPWCDRCQQRWVACSNCGTVAQARSGTWEAPLCAKCTNPDPTFWGRCPVCTVTWQLSTRPCQRCVLDQRVRDLLGDATGAIRPELVPFHEALTSSERPDVAFAWVSRSQVRDLLERLGHDERPVTHEVLDELPPGKVLAHLRSVLVATGALPSREERLIALEKWITATVQTRSDLAERRILHGYAVWHHLRRFRRRLGEEHATRLQDLNVRCHVTAANNFLDWLTGEGLTLGTCTQTDLERWMADSTVSYRDETGHFVRWSVQHRHAHDLTYGTVRWTGPLGTIDSEKRWDDARRFLNDDTLPTSDRVAGLLLILYAQKIATISQLAVDDVHFDSDTVSITFGTSPVVLPAPLASLVRELVATRRGKAKIGTPEDVSWLFPGGHPGRPLTDSQIGNRLHKIGIRPKQDRSTALFTLAAELPAAILARMLGVHIKVAVQWQQASAGDWAAYAADVSHRTSS
>NZ_LN831790|101352:142427|123426_125913_+|WP_047121429.1|DBSCAN-SWA
MIGLIPTATPVALREVRHDLAGRRVLVIGDCDGLAGAMLARLSAAGAHTEAVMVRETVRPYASSHRGQLLAAEELAVRLTSGPLPDWVLFLPGFTARARPAQAFRPEEGLYAGGMTRTLFHTLSPLGRRWLERGAGGFAVVTRADGRFGLTGARPGDPLAGLLHGTVRALHAELPMIRTVALDVGPSVPLDVVADRLLDLVSDTSHGHVERGLAGSQAYATTLVPAFEQPADIPGAEGRLPLERGDTVLATGGGRGVTARVVRMMAEEVPCRYLLLGTTKLVDVKAALGVGDRDELLHMPAEELEAHKRRQFAAMRRDNPTLLPPAFERHWARISNSLEVLRTLTHVRDLGARAEYLCLDITDGHATRRFADELVRTSGPVQALLHGAGVETSKNLCRKTQDSWERTVAVKTAGLYNLSPVLGDETRLIMLFGSAAGTYGNPGQIDYAGASEFLTTAAYRLAADFPAARVRSVAWPAWAEVGMAVRPSSRAALEQRDVRFMEVSEGLDWAGALLRSPSRVPVCVSLGYEGMPPEATATRETAPWRSARANRGNLVDLCSEAGPGRWEVRWTYQPELDAALADHQVDGNVRVPFALFIELMCQTASACLGDLGAFTLRALRMHQPLTLAPERPRDLRAVIARTAEGTLRVGVESSPIRPDHSWVPVTLQHASAEIEPLTGQKPAPRIDVALKGLEPVSVDHLQERFAANGIVYGPAFREIVSCWRDGALRLAQVRAGAGWKADVRGRSFFDIGLLDLSLQTLVFHPGARHGGLPTAVEELIVHTELGGSRSEGWALVDTGAEKLGVTLADSAGRVMAQIRNLELTARES
>NZ_LN831790|101352:142427|115303_115921_+|WP_029381177.1|DBSCAN-SWA
MPDDLEIPTLCGTGANLLLSVVDLIHQSVPKTVWETERLRKVFGNRTVPMILADGDVMAFGPCPDRTLVASAVLQRHGIRPTIIYHERRVPGFTPSTAHIAMEISVDGRTWMMDFGSRESRLIEGEYYFNPEIEETLALERFNLLDMDVDLMSVTPNQMFGMVATENIDMEHKYDYYEKQSRRYSGQILEDRLALDKTHSVYYEL
>NZ_LN831790|101352:142427|106105_106279_+|WP_157840681.1|DBSCAN-SWA
MRIPRWITASLFTTAAAVSALALSSGFSLANNDSHHRDSVTTAGQYTTLCLNGGCAD
>NZ_LN831790|101352:142427|140961_141306_-|WP_029381469.1|DBSCAN-SWA
MAAKLDYHWHLRKVMADRGMFSTTDLIPPLKERGISLSSSQVYRLVVERPERLSLKILMALLDILDCTMDDLIEPIAVAGAATKPKKAAAGGSSVSEGVGDLRPRRARISGVDR
>NZ_LN831790|101352:142427|103389_104169_-|WP_157840679.1|DBSCAN-SWA
MAEARPSALEAERDSDIYDPLPHLVLPIQKYIESDDQRRFVAQAAMALVDKCLADKRIKFRLPRRTPDKLPTLMAGRYGPVNQKQAQHGYHYMAVLNGGGSQPSISPNPQESKALSACSDKAEESIPQLEDKNLPEQIKASSYIAATRLPSVVKAFKGWSDCMAETGHKYDSPMDAMNDPKWNWKTAKATPHEVSVATRDVECKKSSGVVQMWFEGEVALEEKKIAEHESALQDVLSQMKQRERSAREVLAKENGHSAT
>NZ_LN831790|101352:142427|128476_129859_+|WP_107408999.1|DBSCAN-SWA
MNRADPRPLHDEDRHALAALRAHGYQVHDIQDIAHDQRSFAVRVPSRRRLLAPGVRFASETVELGDGAFTNAHTLRLNLDHINVEAVTTTEGFHLRDQCTADGVVAAVNGSFSYISDDPAHQPAEPCLDFCCRAGTTVSLPTVTKPAFLVHGDRLMVRTLPATGTLRIGDRLFEWIGSKEPRASADLADGALVVFGAANCRIRYADHPRTGFVRFVRPEENITPKARSVVDAVVSRTTAGSHVISSVHPGGGAELFTGSFILRADAAHARELRSGARVELCTIAGLAADLLTNGVSLGPSVADAATGAVPAYDESLGVSPFRDVRYARTLVWTTRREIVFRVFDGAPLTDSFRGVSPTEVADLLGREGVDLRDAYHLDGGQSSKIVFREGGRTGVVGNLHYLKWPQEPETEFRWRGVEGRLLNSCFVLRLRREAEGRTDADTAAADVSCPGIDNGRGGSG
>NZ_LN831790|101352:142427|104343_104808_-|WP_078648199.1|DBSCAN-SWA
MKVKNPKKGDRLMRKIFAVVGMAITVVASTFAFSAPASAATGKCPMDANGIGFCLYYNSNQQGAYYRWGSGTGEVDDLAGYVFPNNGAGAGQPVKNNAASASYSMGGGCVCSNDFVRVFFYSGQQGDYDVVTSNTNVQLVKTYNENASWRSYYY
>NZ_LN831790|101352:142427|115964_116879_+|WP_029381178.1|DBSCAN-SWA
MTEVAYEIERLVKVYPRQTEAATNDVSLSVRAGEVFGILGDNGAGKTTLVRQMVNLLRSTSGEIRLFGRSVPGNPLFVSRTVAYMPQSSMALNRLKVKEAIYFAAHLRGMSRRDAARERDAMIETWQLGPVRDKSSSRLSGGQQRLLQLALATAGRLPVAVLDEPTNDLDPVNRKHVWEVLRKFNAEQGTTILFITHDAIEAERIVHRVGIMRKGSFLAIGQPAQLKRKLLDHMRLEVWLPPGEVPALPADMPQHWKSDDNVVLSVPRDRAPALLSELRLNESIDYRLYSATLEDLYLHYANSD
>NZ_LN831790|101352:142427|131325_131991_+|WP_029381188.1|DBSCAN-SWA
MKNVLIVVAHPDDAEIGMGMRIAWYARNGARVRVHCLTTGTPEQDGAQPRRQECLSAGLLLGVDRYTFSEIPDTRFTEHRGSINAELFAIIREAVPDVVYTHFPGDQHIDHAITSQEVTAVALREAMNLCYFRSPYSTGFEPNLFFMGTHSLMEAKMQALSCFSSQKQLDMEVFRRIASVAHRQHVHHRIVERFAPELEYVEMFQSARRIESAIEAPSMEG
>NZ_LN831790|101352:142427|101352_102240_-|WP_029383686.1|transposase|DBSCAN-SWA
MSELYRLIHAEKAAYPIVLLCRVLKVSRSSYYAWREGEAARRARQAADDALAHEIAVVHIASRHTYGVPRIHAELRRLGRRVNRKRVARLMRERDIRGVTRRKRRSLTRPDVKAQPAPDLIGRDFHAERPGTKLVGDITCLPIAEGWLYLACWLDLATREVVGYAMADHHRAELVVGALDMAHGRGGLEPGCVIHSDRGSEYTSTQFRERIGKFELRQSCGRTGSCFDNAAAESFWALLKEEIGTRTWPDRATARAEVFNFIETFYNRRRLRKHKTFGYLTPAETRQRHQHALAA
>NZ_LN831790|101352:142427|137704_138430_-|WP_157840631.1|DBSCAN-SWA
MAAITLVLVSIVSALVAILGLQSWVAIAAVIAAVVSGSQVVRKEVLIPWRVKSVDNSVARILTREARAGARLGSAVQIAPRRWVTAAHVVAATGTELKLGDTWIQARVIYRDEDLDLAVLTVDRDWPWLSRVSADLPSPGSRVKVTGWTEGRRDKENRDRGLRAVQDYTVQGPVEESLIVLAGAIPPRGFSGAAVTDVETGKVVGVLFNFRPGEMDFHAGLPRMDEVHATPLSCIPSEYLR
>NZ_LN831790|101352:142427|117647_118418_+|WP_029381180.1|DBSCAN-SWA
MSETQTLDGVLASTRLAWSVLFGGESLGEVDRELLRSLQDDPGTWGRLILDTWATFTALDGKRAPAGLSVRRDAGAESVTATASRTDSREEEAVARTEDGMIPEQAQSSSQRAETVASRPAELADQAEGRTGSPAVMAPASSRPEPAPAGTTQPLDFFDPDEEDESVPPRRTVTVEEVKARLTELIAEISGYPEDVFEDHLDLEVDLGIDSIKQVETLAKVREEYDLPLDEGFLMRDYATIGKMAGYIVDRLEKET

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_029383686.1|101352_102240_-|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	9.3e-32	31.1
WP_029383687.1|102236_102536_-|transposase	transposase	A9YX41	Burkholderia_phage	8.5e-06	37.2
WP_157840679.1|103389_104169_-	hypothetical protein	NA	NA	NA	NA
WP_078648199.1|104343_104808_-	hypothetical protein	NA	NA	NA	NA
WP_157840680.1|105011_105248_+	hypothetical protein	NA	NA	NA	NA
WP_029383688.1|105372_105714_+	hypothetical protein	NA	NA	NA	NA
WP_157840681.1|106105_106279_+	hypothetical protein	NA	NA	NA	NA
WP_047121425.1|106871_107417_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_164497180.1|107401_108646_-	hypothetical protein	NA	NA	NA	NA
WP_047122291.1|108946_109294_+	hypothetical protein	NA	NA	NA	NA
109132:109149	attL	NA	NA	NA	NA
WP_047121426.1|109290_109527_+	hypothetical protein	NA	NA	NA	NA
WP_029383693.1|110272_110941_+	M15 family metallopeptidase	NA	NA	NA	NA
WP_078648201.1|112189_113182_+	Ldh family oxidoreductase	NA	NA	NA	NA
WP_047122292.1|113209_114313_+	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_099053558.1|114337_115187_+|transposase	IS5 family transposase	NA	NA	NA	NA
WP_029381177.1|115303_115921_+	hypothetical protein	NA	NA	NA	NA
WP_029381178.1|115964_116879_+	ABC transporter ATP-binding protein	W6JKT0	Anomala_cuprea_entomopoxvirus	9.3e-19	24.9
WP_047121428.1|116862_117624_+	ABC transporter permease	NA	NA	NA	NA
WP_029381180.1|117647_118418_+	hypothetical protein	NA	NA	NA	NA
WP_049976675.1|118421_119216_+	SDR family oxidoreductase	NA	NA	NA	NA
WP_029381182.1|119263_123430_+	type I polyketide synthase	D0R7J2	Paenibacillus_phage	2.2e-11	30.4
WP_047121429.1|123426_125913_+	SDR family NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_049976676.1|125928_127473_+	Gfo/Idh/MocA family oxidoreductase	NA	NA	NA	NA
WP_029381184.1|127469_128480_+	phosphotransferase	NA	NA	NA	NA
WP_107408999.1|128476_129859_+	phosphodiester glycosidase family protein	NA	NA	NA	NA
WP_164497166.1|129899_130406_+	flavin reductase	NA	NA	NA	NA
WP_157840618.1|130558_131329_+	WbqC family protein	NA	NA	NA	NA
WP_029381188.1|131325_131991_+	PIG-L family deacetylase	NA	NA	NA	NA
WP_099053560.1|132194_133045_-|transposase	IS5 family transposase	NA	NA	NA	NA
WP_047122297.1|133337_134291_+|transposase	IS481 family transposase	NA	NA	NA	NA
WP_029381463.1|134287_134770_-	hypothetical protein	NA	NA	NA	NA
WP_029381464.1|134771_135302_-	hypothetical protein	NA	NA	NA	NA
WP_029381465.1|135743_137303_+	protein kinase	A0A146JFA3	Tokyovirus	3.3e-16	30.2
WP_029381466.1|137362_137677_-	hypothetical protein	NA	NA	NA	NA
WP_157840631.1|137704_138430_-	trypsin-like peptidase domain-containing protein	NA	NA	NA	NA
WP_029381468.1|138556_140965_-	hypothetical protein	NA	NA	NA	NA
WP_029381469.1|140961_141306_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_029381470.1|141323_142427_-|integrase	tyrosine-type recombinase/integrase	S5W9T9	Leptospira_phage	2.1e-09	27.9
152353:152370	attR	NA	NA	NA	NA

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_LN831790|2005371:2058129|DBSCAN-SWA
CGTGAGCCAGGACCAGGACCCGACGCCCGTGAACGCCCCGCCCGCCCGCCCCGCGGCCGGCGCACCCGAGTACGTACTGCCGCTCGTCGTCCGCATCGAGCGGGCGGCCCCGCCGCCGCGGACGGACGCGCTTCAGACCTCGGCCCGGGCGGTGCTGGTCATGCTCGCCGACGAGCGGTCGGTGGGCGACGGCGAGTGGGCGCAGGCGATGCGGGACTGGCAGGACGCCCGGATCCGCAAGGTGGTACGGCGGGCGCGCGGCGCCGAGTGGCGGCGCGCCGAGGCGCTGCCCGGCATCACGGTGACCGGCAAGGCGGCCGAGGTACGGGTCTTCCCGCCCGTGCCGCTCGACGGCTGGCCCAAGGACCTGGCCCGCCTCCAGGTCTCCGGCACCGACCTCGACGACCCGGAGGCCCCCGTGGACGCCGACCCGTCCGCGCCGGTGCTCTGGCTGAACCCGGACCTGGAGATGTCGGCCGGCAAGGCGATGGCGCAGACGGGCCACGGCGCCCAGCTCGCCTGGTGGGCGCTGCCCGACGAGGAGCGCGCCGCCTGGCGCGACGCGGGCTTCCCGCTCGCCGTGCGCACCGCGGACCCCGCCGACTGGCGCCGCCTGACCACGAGCGGCCTGCCGACGGTCCGCGACGCCGGTTTCACCGAGGTGGCCCCCGGCTCCTGCACGGTGGTCGCGGACCACCCGGCGCTGCGCTAGCGGGCGGCCCCGCCGCGCCGCTCCCGGACGAACCCGGTCAGCCCCAGGTGAGCGGATCGAGATGGAGGTAGAAGCGCAGGCGGTCGGGGTCGACGGCGATCCCGTACCTCTCGGCGAACGCCGCGTCCGCCGCCCGCGCCCACTCCTCGTCCGGCCAGGTCTCGCGCGCGTTGGCCAGCAGCAGCGCCAGGTCGGCGTGGCGGTCGGCACGCCCGAGGCGGCCCAGGTCGATGAAGCCCGACACGTCCAGGGTCCGCGGATCGAGGATGATGTTGGGCAGGCACAGATCCCCGTGGCACACGACCGTGTCGGCGGCCTCCTGCTCCCGTCGCCGGGGCACCTGCCCGGTGAGGCGGGCCAGCAGCTCCGCGGGCGGCAGATGCTGCTGCTCCACGGGGAGGAACTCCGGATTCACCGCGCCCCGGGCCACGACGTCGCGCGCCAGGGCGAGCATCGCGTCCAGTTCCCGGCCGAACGGGCACTCCGCCACGGGCACCTCGTGCAGCCGGCGCACCGCGTCCGCGATGCGCCCCCAGGACAGGCGCAGCTCCTCGGCGGACACCTGATCGGCGGGGACACCGGAGACGGCACTGGTCACCAGGCACACACCCGCCTCACCGGAGTACCAGTCGAGCACCCGCGGCCCGGGCACGCCCCGGCCGTTCAGCCACTCGACCCGGTCCCGCTCGGCCTCCAGCCCGGCCGCCTCCGCCGCGGGCACGCACTTGGCATACCGGGCGGCATCCGCACTGCGGAAGACGAAGGCCCCCGACTCACCCGCGGTGACGGGCAGCCAGTCGCCGCTCCCCATGCCGAACAGCGCCGGCGACACGGTCGGGGGTCCGGGGTGGTCGCTCATGACGGCAACCTTAGAGCCCATGGCGAGCGTTGCCGGCGCCAGCGCCAGGCTCCGCCGCGGAGGGAGGGCCGAGCCGCCAGCCGACGACTGATGACGGACCGACCTGGCCGGTCTTGCGGCCAGGTATGAACTCGAGCCCGCAACCGGATTCGAGATAGTGGTTCACGTGGCGCCGTGGCGCCGTCTTCGGGATATGTCGTGCATGGGCAAATACTTCCGGATATTCGCCATCTAAGCCGTCACTGGAAGCCATTCATGTCGCCCGAACAGTACATGACCTTTGATAAGTCTTTTCCAGACACACACAGGCACAGGGTTGACTGAATGACCCATCTTTGCTTGCCGAGTTGATCGCGGGTGCCTACTGTCTGATCGTTATTCGCCCGGCCACGTAGACGCGTTGGCCGGATCAGGGTGAGGGGGGAGGTCCCCTTTGTGGATCAACTCATAAGGCAACTGAGGTATTTGGGGCATTGGCACAGATCCGTGTCCCTCTTCGTCGGCATGGTGATGTTCGTCGGGCTGATCCCCGACGACGCCAGTGCCGCTTCCGGGAGCAGCAGGGTCCCGGACGTGAAACGGGAACCGTCCGTGCCGGGCCGCGACTTCACCAAGAAGCGTCCCGGGATCCGTAACGACGCCGCCGTCGACTGGCGGCCCACCGCGGGCACGGTGTCCTCGCAGAGCTTCACCACGCAGGTGACCGGCGGCGGGGGCGAGAGGGCCGGGCGGGCGCCGCTGCTGTCGGGCTCCGGCGGCGGGGAGGCGGCCGGGGTGCGCACGAGTCCGGTGCGTATCCGCAAGGCCGGGACGATCGGCAAGCGGGACGGTGTGCGGATCACCGGCCGCGCCGCCAAGCGGGCCCCGGCCGCGCCGGGCAGCGCGGTCCGGGTGCAGGTCAAGGACATGGCCACCGCCCGCAAGGCCGGTGTGCAGGGTCTGCTGCTGACCGCCGAGCCCGCCACCGGCGCCACCGCGCCGGCCGCGTCCGGCTCCGTCGACGTCGAGCTGGACTACTCCTCGTTCAAGGACACCTACGGCGGTGACTGGGCCTCCCGGCTGCGCCTGGTGCGGATGCCGGCCTGCGCGCTGACCACGCCGGGCAAGGCGGGCTGCCGCACGGTCACCGAGCTGCCCGGTGTGAACGACCCGGTGGCCAGGACGGTGAGCGCCACCGTCGATCTGGCCCCGGCCGGCGCTCCGACGGTGCTGGCGGCGACCGCGGCCGCTTCCGGTCCCGGCGGCAGCCACGAGGCGACGTCGCTGTCGCCGTCGGGTTCCTGGATGGCCGGTTCCTCCTCCGGCGGCTTCGCCTGGACGTATCCCATCGAGGCGCCCGAGGTGCCCGGCGGCCCGCAGCCCGAGGTCGAGCTGTCCTACTCCTCGCAGGCCGTGGACGGCCGTACCGCCTCCACCAACGCGCAGTCCTCCTGGATCGCCGAGGGCTGGGACTACGAGCCCGGCTACATCGAGCGCCGTTTCCGTTCCTGCTCCGACGACAAGGGCGAGGTCGGCGGGGTCAAGCCCAACAACACCGGTGACAGCGGTGATCTGTGCTGGGGCTCGGACCATGTGGTGATGTCGCTGGGCGGCAGCACCACCGAGCTGGTCAAGAAGGACGGCACCGACGAGTGGCGGCCGGCCGACGACGACGGCTCGCGCCTGCAGCGCAAGACCGGCGCGGCCAACGGCGGACACGGCGGCGAGCACTGGGTTCTGACCACCACCGACGGCACCCAGTACCACTTCGGCCTGAACAAGCTGCCCGGCGCCCCGGAGGGCACGGTCACCAACTCCGCGCTCACCGTGCCGGTCTTCGGCAACCACCCCGGCGAGCCCTGCCACGCCACGGCGTTCACCGACTCCGACTGCGCGCAGGTCTACCGCTGGAACCTGGACTACGTCGTCGATCCGCTCGGTGACGCCATGACGCTGTGGTGGACCAAGGAGACCAACCACTACGGGCAGAACATGAAGGCCGATCAGCCGGCCTCCTACGTGCGGGCCGCGCAGCTCGCCCGGATCGACTACGGTCTGCGCTCGGACAAGCTGTTCGGTGTCCTGCCCGCGGGCCGGGTCTCCTTCACCACCGCCGAACGCTGCATCCCCAGCACGGCCTTCGACTGCGCGGAGTCCAAGCGGACCGCGGCCAACGCCAAGTACTGGCCGGACGTGCCGCTGGACCAGGAGTGCGCGGCCGGTGCCAAGTGCACCGACAAGTACTCCCCGACGTTCTGGACGACCAAGCGCCTGACGAAGATCACCACGCAGGTGCTGTCGGGCACCGCCCTGAACACCGTCGACTCCTGGACGCTGGAGCAGTCCTACCCGGCCACCGGTGACGGCACCTCGCCGGCCCTGTGGCTGGACTCCATCACCCGCACCGGCCACCGCGCCGGAGCCACCGCCGCCATGCCGAAGGTCACCTTCTCCGGCACCCAGATGGACAACCGCGTCGACGGTGTGGAGGGCCTGCCGCCCTTCTCCCGCCAGCGGATCCACGCCATCGACACGGAGACCGGTGGGCGGATCGCGGTGTCGTACTCGGCGCGTGAGTGCCAGGCGCTGGAGCCGCGGAAGATGCCGGCCTCGCCGGAGTCGAACACCCTGCGCTGCTATCCGCAGTACTGGACACCGAAGGGTGCGCTGGCGCCGGTCAAGGACTGGTTCCACAAGTACGTCGTCACGCAGGTCAGTGAGCAGGACCTGGTCACCGACAGTCCGTCCAAGGTCACCTCCTACGAGTATCTGGGCAGCCCGGCCTGGGCCTGGGACGACAGCGAGTTCACCGAGAACAAGCACCGGACCTGGTCGCAGTACCGCGGTTACGAGCGGGTGCGTACCCGTATCGGCGGCGGTACGGACGTCAGGCAGCTCACCGAGCACCGCTACTTCCGCGGCCTGCACGGCGACAAACTGCCCTCGGGCACCCGCACCTCGACGGTCACCACCAGCGACGGCTCGAGCTTCCAGGACCTGCCGCAGTACCAGGGCCAGCTGCTGGAGCAGATCACCTACGAGTCCGACGGCGGGCCCATCGACTCGGCCACCGTCACCACGCCCTGGTCGGTGAAGACCGCCACCCGCACCCGCAGCGGCACCACGCCGCTGGAGGCGTGGATGACCCGCCCGGAGAAGGTCCTCACCCGCGAACGGGTCAAGGGCGAGACCTGGCGCACCTCCACCGAGACCACCGCCTACGACAGCTACGGCCTGCCCTACCAGGTGGAGGAGAAGTCGCCCGGCGGCACGGTGCGCTGTTCCACGGTCACCTACGCGCGCAACACCAGCGTGTATCTGATCGAGCTGGAAGCGCGTGAGAAGACCGTGCTCGGGGCGTGCGGCACCACCGGCGGCGAGGTCGTCGAGGACACCCGCACCCTCTACGACAACCTGGCCTTCGGCGCCGCCCCGGTCAAGGGCCTGCCCACCGAGATCCAGGAACTCGACGGCACGGGCGAGGGCTACCTCACCATCGACCGCACCGAGTACGACATCCACGGCCGCGAGATCGCCACCTGGGACGCCGACAACCGCAAGACGTCCGTGGTCTACACCCCGGCCACCGTGCAGCGCCCGGTCAGGCAGGTCTCCACCGATCCCCTCGGCCACACCGAGACCACCGACTTCGACACCCTGCGCGGACTGCCGCTGGTGGAGACGGACGCCAACGGCAAGAAGGCCACCATGGAGTACGACCCGCTGGGCCGGCTCCTGAAGGTCTGGGAGACCGACCGCGACCCGGCCACCCAGACCCCGACCGCGACCTACGACTACACCGTGCGCCGCGACGGGCCGACGATCGTCACCACCCGCACCCTGAAGGACAACGGCGAGTACGCCGTCTCCTACGAGATCCTCGATGGACTGCTGCGCGAGCGGCAGACCCAGGACGAGGCGATCGGCGCGGGCCGGATCGTCAACGACACCTTCTACGACAGCGCCGGACGGGTGTGGAAGGAGAACGACGGCTACTACAACAGCGCCGAGCCCGAACCCGTCCTCCTCCAGGTCGGCGACAACGACGTCCCGTCCCAGAACCGCACCACCTTCGACGGCCTGGGCCAGCCCACCGCCGAGATCACCTACTACCGCGGCACGGAGAAACTGCGCACCACCACCGAACGCGACGGTGACGTCTCCACCACGATCCCGCCCAAGGGCGACACCGTCACCGCCGTCTTCGAGGACGCCGAGGGCCGCACCGAACGGCTGCGCGAGTACACCGACGCCGCACGCACCAGGTGGCGCGACACGGTGTACGAGTACGACGACCTCGACAACCTGGTCAAGGTGACCGCCCCCGGCGGCGCCGTCACCTCCTTCGAGTACGACAAACGGGGACGGCAGACCGCCGTCGTCGACCCCGACGGCGGCCGGACCGAACTGCGCTACGACAACTCCGACAACGTGGTCGCCGCCACGGATCCGGACAAACGCACCCTGGTCACGACGTACGACGCGGGCGGCCGGCCCACCTCGCTGCGCGAGAACAGCGAGACCGGTCCGAAGCGGATCGAGTGGACCTACGACACGGTCGCCAAGGGCCTGCCCACGGCGGCGATCCGCTACGACAACGGCCTGGAATACCGCGAGGAGATCACCGCGTACGACGACGCCTACCGGGTGAAGTCGACCAAGACGGTGATCCCCGCCGAGGAGACCGGCCTGGCCGGCACGTACGAGTACAAGTACTCCTACACCCCCACGGGAAATCTGGACTGGGCCGAGGTGCCCGGCGTGGGCGGCCTCGTCACCGAACGAGTCGTCTTCGTCTACAACTCCGACGGTCTGCCCATCGCGATCGGCGGCGCGGCGCCGTATCTGACCAACGTGCAGTACTCGGCGTTCGGGGAGATCCTGCGCAGCGACTCCGGTCCCGCGGGCAAGAAGGTGTACGGCAGTTACGTCTACGACGAGTTCACGCGCCGGCTGCAGTCGGCCACCTTCGACCGGTCCGTGGCGCCGCTGCGGATCAGCGAGACCAAGTACGCCTACGACGAGGCGGGCAACGTCACCAAGATCACCGACACCCCCGGTGACGCGGCGCCCGACGCGGGCAAGACCGACACGCAGTGCTTCGTCTACGACCAGCTCCGGCAGATGACCTCCGCCTGGTCGGCCAAGACGGACGACTGCACGGCCGGCCCGTCCAAGGAGACCGTCGGCGGCCCGGACGCGTACTGGCAGTCCTTCGAGTTCGACGCGGCGGGCAACCGCACCAAGCTCGTCGAGCACGACCCGACCGGTGACACCACCAAGGACGTCACCCGCACCTACATCTACGGCAAGGAGGGCATCGGCGGCCCCAACGCGCTCGCGGAGATCAGGTCCGTGGGCCCGCAGGGCGAACGCCTCAACACCTTCGGCTACGACAAGCGCGGCAACACCACCCAGCGGCAGCACGGCGGCGCCACCCAGACCCTGGAGTGGGACGTCGAGGGTGAGCTGCGCAAGGTGACCGAGCCGGTCGAGGGCGGCGGCACCAAGACCACGTCGTACCTCTACGGCGCGGACGGCGAACGCCTGATCCGCCGGGGAGCCGACGGCAGTCGCACGCTCTACCTGGGCGATGCGGAGCTGACCGTCAGCGCCGACAACACCAAGAAGACGGCGGAGCGTTTCTACGCCCACCCCGACGGGATGACGACGGTCCGCGCGACCGGCGGCGTCCGCCAACTGCTCATCTCCGACCACCACGGCACGTCCCACACGGTCGTGAACATGGCCGAGGCGACGATGGGCGTCACCCGCCGCAAGTCGCTGCCGTTCGGCGAGGCCCGGGGGCAGCAGCCCACCGCCTGGCCCGGACAGCGGGGCTTCGTCGGTGGCACGGTCGACAAGGACACGGGCCTGACCCGGTTGGGCGCGCGTGACTACGACCCGCTGACCGGACGGTTCGTCTCCGTCGACCCGATGGTCGACTACGGCCAGCCGGCCACGATGAACCCGTACGCCTACAGCAACAACGCGCCCGCCACCTTCTCCGACCCGACGGGCGAGTTCTTCCCCGTCCTGATCGGCATCGCGGCCCGTATCGCCATCCAGGCGGCGATCCGCGCGGCGGCCCGCCGCGCGGCGATCATCGCGGCCCGCAAGGCGGCCCAGGCGGCGGCCCGGCGCGCCGCGGCCCTCGCCCGCAAGCGTGCGATCGAGGCCGCCAAGCGTGCGGCCGCCCGCGCCCGCCGTGAGGCGGCCCGCAAGGCGGCGGCGGCCCGGCGGGCGGCGGCCAAGCGGGCAGCGGCCCGCGCGGCGGCCAAGCGCGCCGCGGCCAGAAGGGCGGCGGCCCAGGCTCGCGCCCGCGCGGCCCGCGCCGCGGCGAGGAAGGCGGCGGCACGGCGAGCGGCGGCCCGCAAGGCCGCGGCCCGGCCCAAGCCGCGCGCCAAGCCCCGCTCCCAGCCCAAGCCCCGCCCCAAGCCGCGCCAGGTGAAGCGGGCGGTGAAGAAGGTCGCCAAGGAGGTCCGGGAAGAGGCCAAGGAAACCGTCAAGGAAGAGGCACAGGGCGCGACCTGCGAGTCGAACAGCTTCACACCCGGCACCCGGGTGCTGATGGCGGACGGCACGACCAAGCCCATCGAGAAGGTCAAGGCCGGTGACAAGGTCGTCGCCACCGACCCGAAGACGGGCCGTACCTCCGTCCAGACCGCCTCCGCCACCATCATCGGCAAGGGCACCAAGCACCTGGTGAAGGTGACGCTGTCGGTCCACGACGGCTCCGACCGCGACGGCACCAGGACCACGACCGTCACCGCGACGGCCGGCCACCCCTTCTGGGTGCCGTCCCTGCGGGAGTGGATCGACGCCGGTGAGCTGAAGCCCGGACAGTGGCTCCAGACCTCCTCCGGCACGTGGGTCCAGGTAACGGCGATCAAGGCGTGGACCGCCCACAAGGCCACCGTCCACAACCTCACCGTCACCGACGTCCACACGTACTATGTGCTGGCGGGGTCCAGGCCGGTCCTCGTCCACAACTGCAACGAAAACATAATCTCCAACGCGCCAGGGTTCGACAATTCAGCAGAACTCTCCCGCGTCTCCGACGGGGATGTCTACAGCGGGGTTTACGAGCCGAGCAGCGGGACGTTCTATGCCCGTCTGAGTCTCGACGAGAAGGACCCCGCAAGATTCCCGAACGCCGTCCTGTCGAACGGTGGGCACGGAGAGGTCAACTTCTGGCACTTCAAGGGCTCGCGAGAGACCATCGGGTTCAACATGTTCTTCGAAAAGGGCGGCATATCGGTGGCTTGGTTCTCCCGAAGCGTGAACAGGAGGAATCACGGGGATCCCATGGCACCTTCAGGTGCACGGCAGGCGATCATGGACGCCATCTCCGGCGCCACGGGCAGGCGGGTGTGGTCGCGGTGAACGGCGACGGGGAGTCCTGTGAGCCGATTTTCGGCATGCCGCTCCCCGCTCGCCTCGTCACAGCGATACGAGATCGCAGTTGGATGGATCTGGCCAACTCCCCGAACCTCGAGGAGGTGTTCGGCCAGGCCCCTCTGCGACCCCGTTTCTACTCGATCTCCGGAATCACCGCAGCGACGAAGTGGTGGCGCGACGAGCTCGACGAGGAAACCCTGCAGTGCTACCTCGGCACATCCGAAGAACATGCCGCGCCTGGGCATATGTCGCGGATGAAGACCGTGATCATCGGGGACCTGGGTCCGGATCTTCCCTTCGTCTTGGACTACCGCGATTCCTTCGCCGATCCAAGCGTTGCCTTTCTGGGGGAAGGTGATGCCTGGCGAAGGGTCTCCGATAATGTCCGCGCCCTGCTCGCCATGCTCGACGGGCAACGGCCGGACGCCTAGCCGTGGGGGTGTCCGTGGGGGCGTGAGGTGCGACCTCCTCCCTGATCAGCCAACTACCGCACCGGATAGGCAATAGCACGTATGGAGCCCCGCCAGGAATTGTCCTGGCGGGGCTTCTGCGCGTCGTGACGGCAGTGGCTGACGGCAATGCGTCAGCGAACCGGGGGCGGCGCGAGGTGGCGGTTCATCGCCGTCGCCGTGCCCCGGCCGCCGTGCTCCGGCCGGGGCACGGCCGAGCCGTGCCGGGGCGCCGTGTCGCTCTCCGGTGGCCGGGGTGCGGGGGTGGTTCCACGTTGGCCGGAGATCCGCCCTGGACGGGCGGAAACCGGTCGAACGAGGAGGACGGATCATGGCGGACCAGCAGACCGGCAGCGGCTTCTCGATCAAGATGTGCGATCTTCCGGTGACCCTGCCGGCCAGGGAGGACAGCGAGTGGTCCCTGCGGGAGATCCTCGAATGGGCTCCGGAGCACTCCGACTGGGGGGCGAAGAGGATATGCGTGGCGGGTTGCGGGGTGACCTGCCTGGAGGTGCCCGAGGGGACACTGATCGAGGTGCCCACCGAGGACGCCCTGGACATGCGGCTGGTCGCCCCGGCGGAGGTCGAGCGGCGGCTGGCGGAGAACCGCCTGTGGCGCGACCCTGAGTGAACCGCCTGTGGCGCGACCCCGAGTGAGGGATCACGCCCGCTGGGGCGCGCCGCCCGCCGCGCCGGCCGCGCTGACGATGCGGTCCTGGAACTCCGCGTGACAGAAGTGGTACACGGGCCCGACCCGTCTGAGCACACTGAGCATCCGGGCGTCCTCCAGGAACGACAGGGGACGACTCTGCAGCCGTCTGGCCGCGGCGAGCCGTAGCCCCGCCCCGCGGTAGGCGAAGTAGGCGGTGCCCGACACGGCCAGCAGACCCGCGGCGAGCCCCATCGCCACGTTCGCCTCCAGGGTCTCCAGCCAGCGGCCGACGGCGTCGAGGGCCTGGATGTCACTGCCCGCGAAATGTCCCTCGAACGCGATGAACCACTTGGCCAGGAGCGGCACCAGCGCGAACACCAGCAGGGCGGCGGCCGCGGCGCGCTCACCGCGCAAGGTCGACTGCGGCGTTTCCTGCTCCAGGTCGGCCGGGACCCGCGCCCAGCGCAGCACCGCCAGACCGAGGCCGAACAGGAGCCCGAAGAAGGCGCCGAAGCCGCACGCCACGAGCCTCGTCGACCAGGCGATCATGGGGCCCCAGGGGGCCGCGAAGGCCAGCACGACCCCCAGGACGGAGCCGAACAGCAGCCCCCGGCCGAGGCAGGCGGGCAGCACCCCCGCGAGCACGCGGACCGGGGCGCGGAAGTCCAGACGGGCGGGGCGGGACGAACCGCCGGACAGGCGCAGTCCCGCCATGACACCGGCGATCAGCAGCAGGACACAGGCACGGGAGGCGGCACGCCGGCTGACGAAGACCAGGTCCTCGGCCGGGGTGATGAAGACGATCCGGGTGGGGGGCTCGCCGGTCACCTGCCGGAACGGCATGTACAGGAGGATGCCGGCGGCCTGGGCACCCAGCCAGAGAAGCACGACGTACAGCAGGATTCTCCGTACCTCGGCGCCGAGGTCGCCCGCCGGGCGGCGGCCCGCCCGGGCACGCCGCCGCAGTGCTGTCACGCACAGGGCGCCGAGGGCCGGCACCACCATGAACAGGGCCCAGGCGATGCCCGCCTTGATCCCGGTGTACGGCGGCGCGATCACCTCGATGTCCGTGTCCGCGCGTTCCACCGCCTCCGCCCAGTACTCGATGAGCGCTCCCATCCCCGCAGCCAGCGGCAGGACGACGGCGAGTGCGAGCCCGATCCGGCGCAGGACCTCGCCGGTGATGTGCCGCCCTCCCCCGGCACGGTCCGGCCGCCCGGGGCCCCTGGGTCACCGCCGACATGGGCGAGCCGGATCACCACGCCGGCGCCGACCGCCGTGGCGAGCGTGACGGCGAGAAAGCACAGGACCCGCGTGAACGGTGGCAGCGCCCAGTGGAAGTAGTCCCCCGCCATGCACCCCGCCCCCAGTCCGATCATGGCGCCCGCCGCGGGGCCGGACAGGGGGCCCGCCGGGTCGGGGCGCAGGGCGCGGTGCAGGTCCCACCAGGCGATGCCGTCGGTGCGCTGGCGTCTGACGTGGTCGGCGAGGAAGGCGAGCGCGGTGCGGGCGTCGTCGGGGTGCCAGCGGGCGGCGGCGGTGCGGCGCACGTCGGGGACCGAGCGGTCGGTGGCGGCCGGCGGGGCGGTGAAGACGGCCGGGACCAGCGCGTCGAGGAGGTGGTGGCGGATGGTCTCGGCGTCGTTCCAGCGGGTCAGTTCGGCGGGGTCGGTGCCCGGGGAGCCGTAGACGGTGCGGGCGAGCCAGACGTTCAGCGGCACCGACAGGGCCTGCGCGACGGCGCCCCGGGGCCGGCCGGCCAGGTCGTCCAGGACCGGCTGCCAGGCCGGGATGTGCCGGGGCGGGACGGCGCTGCGCAGATAGTCGACCACGTCCGCGGCCTCCACCGGCTGCGCGACGACGACGGCGGCGGCGGTGATCACGTCGGCCTCTTCGACCAGCCGGTGGTATTCGGCCCGGCGGGAGGTGAGGACGAGCGGGTCGTGCAGGGCGATGGCGTGGTTGACGGAGGCCAGCGCCTCGGGCCGCAGGTCGGCGGGGATCTCGTCCAGGCCGTCCAGGACGGGCAGGACACGTCCCTCGGCGACCAGTTTGCGTGCCGCGTCCCGGCCATAGGTCTCGTGGTCGCGCAGCGCCGGGTAGTCCTCGTGGATGCGGCGTGCCATCCACGGTGCCAGTGGCTCCCTGCGCGGGTTCCACGACGCCAGGTCCAGCAGTACCGGGACGGGCTCCCCGGGTTCGGGGTCGCGCAGGAGTTCCCTGACGAGCAGGATCGCCAGGGCCGTCTTGCCCGCGCCGGGCTCGCCGACGATCACCAGCCGCCGGCGCGGCAGGGCGCGGAAGGCCGCGGCGAAGGCGGGGATGTCGTCGCTGCGGCCGGACAGGGTGCGGCCCACCATCCGTACATGGTCGCCGGCCTCGCTCTGGCCGCTGCGCCAGCGCACCGCCAGCGGGTGCGGGTCCAGCAGGCCCTGCGCGGCGGCCTCCTCCGTCCACTGGCGGCGCACCATCGCGGCGAGCGCCTCGGCGGCCTGGTCCAGCTCCGCCCGGGTGGCCGGCGCGGCGGGCCGCGACCGGTGCCACGACCAGCTCAGCAGCCCCGCGACCGCCGAGATCACCACGCTCAGCGACGTCGCGGCCGCCTGGGCGCCCGCGCCGACCACCAGGGCCACCACCGTGACCAGCACCACGACACCGACCGCCCCGACCGCCCACGGCCACCACGTCCTGCTCCGTGCCATCACGGGGATCTTCCGGTCCGGGGTGGTGCGGTGCGTGCGGCGCCGTGCGCGGCGTGGCCCCCCGGGGGCACTGACCATGGCGACACTCCCTCGCACCGTCCGGCGATTCGCGCGGTCGGCCACCGGTGCGGGCCGCCGGGGCGGTGCGCGTACGGCGGCGGTGGCTCGCCAGGAGCCGAAAGCCACAAGCCGGTGAGCCGCCGGCCCTCCGGCCGGCCCGTCCCGGGGGCCGCTCCGGCACGCGTCGGGCGCGACGCACGTGAAGGGGACGGTTGATCGATCTCGCTCGGGACCGCGGTGCCCGGGCGTGCGCCGAGCGCCTACGGCCGGGTCAGGGCCCGAGCGCGTGCGTGGGCACCTCGTTTCAGGGTGGCACAGAGTGCGCGCGGGCGCGATGCGGCACAGGGCCTGCGCCGCGCCGCCGCCGCGGAAGTGCGGGCCGGGGCGAGCGCGGAAGCTCAAATGTTGCTCTGAACGTGCCCGCGCCGGGGTTGGGGCACGGAGGGCCGGGGCCATACCCCCCTCACCGCCGGGACGGCATTCCGGCGTGCGGAGGAGGGGGACGATGGAGCGACTGGGGACCGGTATCGGGTGGCGGCCGGAGATAGCGGACGCCGTGGAGCGCATGCCCGGCATCGACTGGGTCGAGGTCGTGGCCGAGAACGTCTGCCCCGGCCACCTGCCCGCCTCCCTGCGGCGTCTGCGCGAGCGCGGTGTCACCGTCGTACCGCACGGCGTCTCCCTCGGTCTCGGCGGTGCCGAACGGCCCGACCCGGACCAGCTGACCGCGCTGGCCGAACGGGCCCGGGCGCTGGACGCGCCGCTGGTCACCGAGCACATCGCGTTCGTCCGCGCGGGCGGGCCGCTGACCGCCACCCCGCGTCTGGAGGCGGGGCATCTGCTGCCCGTGCCGCGCACCCGGGACGCCCTCGACGTGCTGTGCGAGAACGTCCGCGTCGCGCAGGACGCGCTGCCCGTGCCGCTCGCCGTCGAGAACATCGCCGCCCTCTTCTCCTGGCCGGGCGAGGAGATGACGGAGGGGCAGTTCCTGTACGAGCTGGCCGACCGCACGGGGGTGCGCCTGCTGATCGACGTGGCCAACCTCCACACCAACCACGTCAACCGCGGCGAGGACCCGGCCAAGGCGCTGGCCGAGCTCCCTCTGGAGGCCATCGCCTACGTCCATGTCGCGGGCGGCTTCGAACGCGACGGTGTCTGGCACGACAGCCACGCCCACCCCGTCCCGCCGCCGGTCCTCGGCATCCTGGCCGAGCTCGCCGCGCGCGTCTCACCGCCGGGCGTGCTCCTGGAGCGGGACGAGAACTTCCCCGCACCGGCCGAGCTGGAGGGCGAGCTGGAGGCGATCCGGGCGGCGCTGCGCGCGGGGCGGCGGCTCGCCACCGGGGAGCACGCCGGGGAGACGGGCCGTGTCCCGGCCGGGGCGGCCCACCCGGCTCACCCGGCTCACCCCTCCCGCCCGGAGGGCCCGGACGGCCCGGTCCCGCCCGCCGGGGCGGGGGAAGGGCCCGTGGACTCCCCCGGCACCGGGCCCGCCCGGGAGCGGCTCGGTCTGGCGCAGGCCGCGCTGCTGTCCGCGCTGGTGGCGGGGACGCCCGCGCCGGAGGGGTTCGACCGGGTGCGGCTGCGGGTGCAGACGCGGGCGCTGGCGGCGAAGCGGGCGGGCGTCGTGGCCAAGGTGGCGCCGGAACTGCCGGAGATCCTCGGGGACGGCTACCGGCCGGCCTTCCTCGCCTACGCCCACGGCCGCCCCATGACCGGCGGGTACCGGCAGGACGCGCTCGACTTCGCCGAACGGCTGCTGGGCGATGGCCTGCCGGTGGACGCGCGCGCCCGGCGCGCGTTGCGGCAGTGGTGGCTGGAGCGGTCCGGGCCGGTGCCGCGCTCGCGGCGGCCCGCCGTACGGCTGGCCCGGGCCACTCGCCGCGTGCTGCTGCGGCGCTGACCACCGCGCAGGGCGAGAACGGAACGCCACGTCACATACCGGCGACGCTGCGTCCGCATGGTGAAAAGGCATGGCGCGCCCGGCGCCCCTGGCATACAAACGCGGCATGTTCTGGGTCCTTCTCCTGCTGCCGGCCTGGGTCCTGGCCGGCACGGCCTGCGCACGGCTGTGCCTGACCGCGGTCCGCACGGCAGCCACGGACACGGCCGGCGCGGACGCGGGCGGCGGACGCGCCCTGACCCTCTACGAGGCGGCGTTCCTGTCCGGCGGCCCCGGACGGGTCGCTGATCTGGCACTGGTGACCATGGCGTGCCGGCGCCAACTGCTGCTGGCCCACACCGGCTGGGCCACCGTCGTCGACCCGCGCGGGCGGGACGAGATGGAGCGGTCGGTCCTCGGGGCCATCGGGCCGGGCGGCCAGTCCCGGATCGCGCCCGTGCGGGCGTCCGCCGCCACGGCGGACGCGGTGCGCGGGCTGGCCGAGCACCTCGTCGGCGCGGGACTGGCCCTGCCGGACGGCGGCCGCGACAGTGTGGCGGCCGCCGTCCGCCGGGTCCGGCTGGCCGCCCTCGCCGTGTGCGCGCTGGGCGCCGCCGCCGTGGCCCTGCCCGTCCCCATGGGCACACCGCGGCATCTGATCGCCCTGTGGTTCGCGCTGCCGCTGCTGCTGACCCTGGGCTGCCTCGCCGTGGCGCGCATGGAGATCCATCCGTACGCGCGGTGGGCCTCTCCCGCCGGGCAGCGGTTGCTCTGCGCGCTCCCCCGGCAGAGCGGCGGCGCGGACGGCGAGCGGACGTTCCTGACCTCCGTGGCGCTGCGCGGCGTCCACGCGATCGGCGAACCGGACCTGCGGGCGGCCTTCGCCCACCGTGAGCGGCACGCCGGGCGGTACGGGAGCTGAGGGCGCGCCGGTGAGCGCCGATCCGCCGCGCGGCGGGCACACCGACGCGCCGCACCGCGGTCCTTGCCTTGCCCGGTGATCGACCCAAACATCCCTTTCATCGCCGCCGTGCTCGGAAGGGATCCGCGATGAGAGCTGCCGTCGTCCACTCGGCCGCAGGGGCCCTGCTCCTGACCGCCCTCGCCGCGGCCCCGGCCGGCGGCGCACCGGAACGGCCGGGCGCGGCGGAGGGGCCCGGCGCGGCCGAGCGGCGCGGCACCGCGGTGGCCGCCGCGCGCGCCGCGGCGGCCGGCATCTCCTTCGGCCCCTGCCCGGACGCGGCGGACCTGCCCGGCGCCCTGCGCTGCGGCACGGTCACGGTCCCGCTCGACTACGCGCGCCCGGACGGGCGGCAGATCCGGCTCACCGTCGGCCGCATGCGGGCCACGGGGAAGGACCCGCGCGGCGGCGGGCGCGCGGTGCCCCGGCAGGGCGCCCTGGTGTACAACCCGGGCGGGCCGGGCGCCTCCGGGCTGTACTTCCCGCTGGCCGGGCTGTCGCCGGAGTGGAAGCGGCTGGCGGCCGCCTACGACCTCGTCGGCTACGCCCCGCGCGGGGTCGCCCCCTCCGCTCCCCTGTCCTGCCAGGACCCGGAGCACTTCTTCCCGGGGCCCGGCCCGGCCCCGCAGCAGCCCTCGGCGTCGTACAAGCGGCAGCGCATCGCCCAGGCCAGGGCGTACGCGCGCGGCTGCGCAGAGCGGTCCGGCGACGCGCTGCGCCACCACCACTCCCTCAACAACGCCCGCGACCTGGACGTGGTGCGGGCGGCGCTGGGCGAGAAGCGGCTGACGTTCATGGGTGCCTCGTACGGGACGTACTTCGGGGCGCTGTACGCGGAGCTGTTCCCCCGGCACGTACGCAGGATGGTGTTCGACTCGGTGGTGGACCCGCACCCCGGGCGGATCTGGTACCGCAACAACCTGGCGCAGTCGGAGGCGTTCGAGCGCCGCTGGGCGGACTTCCGGGCGTGGATCGCCGCCCACGACGGCGTGTACGGGCTCGGGCGCACACCCGGCGCGGTGCAGCGCGGCTACGAGGTGGCGAGCGCCCGTCTGTCGGCGCGCCCGGCGGGCGGCACGGTCGGTCCGGCGCAGTTGCAGGAGATGCTGCTGCGGGCCGTGTACTACGACGATCAGTGGCCGCACCGGGCGCACGCGCTGTCGGCCTATCTGAAGGGGGACCCGCGGCCCCTGATCGACCTGGCGGAGCCGCACCCGGAGGCGGCGGCCGAGGCGGAGAACGCGAGCGCGGTCTACACGGCCGTCGAGTGCAACGACGCCCCGTGGCCGACGGACTTCCGCGTCTGGGACCGGGACAACACCCGGCTGGCGCGCCGGGCGCCCTTCGAGACCTGGGAGAACGTGTGGACCAACCTGCCCTGCGCCTACTGGCCGGCGCCGCGGCAGCGGCCGCTGGAGGTGCGCACCGGGCCGGGTGAGCTGCCGCCGACGCTGCTGCTGGCCGGGGAGCGCGACGGGGCCACCCCCTACGAGGGGGCGCTGGAACTGCACCGCCGGCTGGCGGGCTCGGTGCTGGTGACCGAGCGCGGCACGGGCACGCACGGTGTCGCCGCCGGGCCGAACGCCTGCGTGAACGGCCATCTGGAGGCGTATCTGCTGGAGGGCCGGCTCCCGGCGCGGGACGCGTTCTGCGCCCCGCGCCCGGCGCCGGAGCCGACGAGCCCCGCCAAGAGCTCCGCGCCCTGATCAGGCGAGCCCCGCCACCAGCTCCCCGATGTCCTTGCGGCGGCCGGTGAAGAACGGCACCTCTTCGCGGACGTGCAGGCGGGCCTCGGAGGCGCGCAGGTGACGCATCAGGTCGACGATGCGGTACAGCTCGTCGGCCTCGAAGGCGAGGATCCACTCGTAGTCGCCCAGGGAGAAGGAGGCGACCGTGTTGGCGCGCACGTCCGGGTAGCCGCGGGCCATCTTGCCGTGGTCGGCGAGCATCCGGCGGCGGTCCTCCTCCGGCAGGAGGTACCAGTCGTAGGAGCGCACGAACGGGTAGACGCTGACGTAGTTCCGCGGCGTCTCGTCGGCGAGGAACGCCGGGATGTGCGAGCGGTTGAACTCGGCGGGGCGGTGCAGCGCCATGTTCGACCACACCGGCGTGAGCGCGCGGCCGAGCCTGGTGCGGCGGAAGAGGTTGTACGCCTCCTGGAGCTGGTCGCTGGTCTCGGCGTGCCACCAGATCATCAGGTCGGCGTCGGCGCGCAGGCCGGAGACGTCGTAGGTGCCGCGGATCGTCACGTCCTTGGCGGCGAGCTGGTCGAACAGCTCCTGGACCTCGTCGGCGTACCCGGCGCGGTCCTCCGGGAGCGCGTCCTTCAGCCGGAAGACGGACCAGAGGGTGTAGCGGATGACCTCGTTGAGGTCCTTGGCCAGCTTGCCCTTGTTGGGGATCCGCTCGGGGGCGGGGGTGGAGGCGTCGTCACTCATGGGCCTATTCTCCCGCTCCGCCGTGCAGGCTCTGCACCGGGTGGGCGGTGAGCTCCTGCACAGCGCGCAGGTCGCCGTGGATCTGGTCGACGGCCGCGTAGGCGCTCGCGACGCAGGCCGGGATGCCGACGCCGTCGTACGCCGCCCCGCACACGGCCAGTCCCGGCAGTGCGGCGACGTGCTCGCGGACGCGGGCCACGCGTGCGTGGTGGCCGACCGGGTACTGCGGCAGCCCGTCGGTCCAGCGGGTGACGCGCGCGGCGACCGGTTCGGCGTCCAGGCCGGTGGCCTCCTTCAGGTCGTGCCGGGAGACGGCCACGAGGCCCTCGTCGTCCCGGCCGAGGATCTCCGTCTCGCCGTACCGGCCGACGGAGGTGCGCAGCACCACCAGGCCGGGGTCCTGCTCAGCGATCCAGCCCCACTTGCGGGAGGCGAAGGTGGAGGCCTTGATGGTCCGCCCGTCGACCGGGGGCACGAGGAATCCGCTGCCCTCGGGCAGCGCCCCCGCGTCGGAGCGGCGGTAGGCGAGGGTGACCAGTGCCATGGAGGCGTACTCGACGGCGGCGAGCTCCGCCGCCGCGGCGGGCGCCTCGGCCCGCAGCAGGCGGGCGGCCGCGGGCGCCGGGACGGCGACGACGACCGCATCGGCGTGCAGGACGCGCTCCCCGGCGACGACCCGCCATCCGGTGGGCGCGGTGCGGCGCAGTTCGGTCACCGGCGCGTCCGTGACGATGTCGCCGCCGCGGGCCCGCACCGATCGGGCGACCGCCGGCGGGAGCGTGCCGATGCCGCCCCGGATGCCCATGAAGACCGGTCCGCTCGGCGGGGCGGTGGCCGTCCGGCCCTGCAGGGCGCGGACCGCCTCGGTGAGGGAGGCGTGTCTCCGGGCGGCCTCGAAGAGCTGCGGGACGGCCGAGCGCATGGAGATGCGGTAGGCGTCGCCCGCGTACACGCCGCCGAGCAGCGGTTCGACGAGGCGGTCGACGACCTCGCGGCCCAGCCGCTCGGCCACGTAGGCGCCCACCGCCACGTCGTCGCCGATCTCCGTGCGGGGCAGGGCGGCGTCGCGCTCGATGCGGGCGAGCCCCTCCTCGGACAGCACGCCGGACAGGGCGTCGGCCGTGCCGGGGACGCCCATGACGTGCCCCTTGGGCATGGGGCGCAGCGCCCCCCGGGTCCACAGGGAGGCCGTCGCGGTGGCCGGCGGCTGGAGGCGGTCGGCGAGACCCGCCGCACGGGCCAGGCCCACCGCCTCGGGGCGGCGGGCGAGCATGGACTCGGCGCCGAGGTCGACCCGCACCCCCGCGATCTCGCCGGGCAGCAGCTTGCCGCCGACCCGGCCGGACGCCTCCAGCACCGTCACCCGCGCGCCGCGCTCCAGCAGCCGGTGGGCGGCGGCCAGCCCCGCGATGCCGGCCCCGATGACGACCACATGCCCCGTACCCGCAGGGGTCTCCTCTTCGCGCATGTCCCCAGCCTCTCAGACGGCACCGACAGCGCCGCCCGGCCCCCGGGCGTCCGGCGCGAGTCCCGACCGTGACCACTTCGGAACCGTTCCGCGCCAACGTCCCGGCCGCCCCGGGCGTCGAAGGGACGTCAGATCTCACCACCCCGGGGGGAACCCACATGCGCGCACGACGTTCCGTACGACCCGGCCGGCCCCTGGCGGGGCTGCTGCTCGCGGCGGCCCTCGCCCTCACCGGCTGCAGCGCCGGCGGCGAGGACAGCGCCGGGAGCGGCTCCGCGGCCGACGCCGCGAAGGAAGCCGCCTCGCAGGCGGACGGGCGCGGGGGCGGCGCCTACCGCGGCGACGCGGGCGGCGCCAAGGCGTCGGCACCGCAGAAGCTCACCACCGGCCACATCATCCGCACCGCGTCGCTGACCGTCCAGGTCGACAGCGTCCCCAAGGCCCTCGACGCGGCCCGCGCCGACGCGGAGAGCGCGGGCGGCTACGTCGGCAACGAGACCACCACCCGCGACGAGGACGGCCGCGAACGCACCCGGGTCGTGCTGCGGGTGCCCGTGGAGAGGTACGACGGCGTCCTGGCCGGCCTGGAGGGGGCCGGGAAACTCCTCGAGCGCAGCGCCAAGGCCGAGGACGTCACCGATCAGGTCGTGGACGTGGAGAGCCGGATCAAGTCCCAGCGCGCCAGCGTGGCCCGGGTCCGCGCGCTGATGGACCAGGCGACCAAGCTGAGCGACGTGGTCACCCTGGAGGGCGAGCTGAGCTCCCGCCAGGCCGAGCTGGAGGCGCTGCTGGCCCGCCAGGCGTCCCTGAAGGACCGTACGACGCTGGCCACCATCACCCTGTCGCTGACCGAGACGCCGGTGAGGGAGTCCGAGCGGGAGGACGACCCCGGTTTCCTCGACGCCCTGGCGGGCGGCTGGGACGCGTTCGTGACGATGCTGCGCTGGCTGGCGGTGGCGCTCGGCGCGGTGCTGCCGTTCGCCGCGGTGGCGGCGCTGCTCGTCCTGCTGTGGCTGCGGGTGGTGCGTCCGCGGCGGCCGGGCGGCTCCGCCGGCCCCGACATCTCCGCCGGCACCGGCGGACAGGGCTGAGCGGCCCCGGGCCGCACCTAGCGGCTCGGGTCGGCTCGGGTCGGGTCGGGGCCGGGCGAGCGGGCGGGGCCGAGGGGGAACGGACCGGCCCGTGCCCGTAGCGTGTCCGCATGAGCATGAGCGGTGCGCGGGAGACGGGGCGGCGGCGTCTGGTCGTGATCGGCGGTGACGCCGCGGGGATGTCCGCGGCGTCGCAGGCCCGGCGGCTGAAGGGCCCCCGCGAGCTGGAGATCGTGGCGTTCGAACGCGGCCACTTCACCTCCTACTCGGCGTGCGGCATCCCCTACTGGGTGAGCGGCGACGTCCCCGGCCGGGACCAACTGATCGCCCGCACCCCCGAGGAGCACCGGGCGCGCGGCATCGATCTGCGGCTGCGCACCGAGGTCACCGGGATCGACGTGGCGGGCGGGCGGGTGCGCGCGCGGGACGTCGATTCCGGGGCGGAGTCCTGGACGCCGTACGACCAGCTCGTGATCGCGACCGGCGCCCGCCCGGTCCGCCCGGACCTGCCGGGCGTCGACGCGCCCGGGGTGCACGGCGTGCAGACCCTCGACGACGGCGAGGCCCTCCTCGGCACGCTGGCCCGCACGCGCGGCCGCCGGGCCGTGGTCGTCGGCGCCGGTTACATCGGCGTGGAGATGGCGGAGGCGCTCATCAAACGGGGCTACGAGGTGACGGTCGTCAACCGCGCCGAGGAGCCGATGTCGACCCTCGACCCCGACATGGGCCGCCTGGTGGGCGAGGCCATGGAGGGCATGGGCATCACCATGGTGAACGGCGCCGAGGTGACCGGGCTGCTCACCGGTGACGACGGCCGGGTCCGGGCGGTGGTCACGCGGGACGCCGAGTTCCCGGCGGACGTGGTGGTGCTCGGGATCGGGGTGCGCCCGCAGACCTCCCTCGCCGCGGCGGCCGGGCTCCCCCTCGGCAGCCACGGCGGGCTGCTCACGGACCGGGCGATGCGGGTGCGCGGGCACGAGAACATCTGGGCCGGCGGCGACTGCGTGGAGGTCCTCGACCTGGTGTCCGGACAGATGCGGCACATCGCGCTCGGCACCCACGCCAACAAGCACGGCCAGGTCATCGGCACCAATGTCGGCGGCGGCTACGCCACGTTCCCCGGTGTGGTCGGCACCGCCGTCAGCAAGATCTGCGATCTGGAGATCGCCCGCACCGGGCTGCGGGAGAAGGACGCGCGGCGGGCGGGGCTGCGGTTCTCGGCGGTCACCATCGAGTCGACCAGCCGCGCCGGGTACTACCCGGGCGCTTCCCCCATGACGGTGAAGATGCTCGCCGAACACCGCACCGGCCGCCTCCTCGGCGTGCAGATCGTCGGCCGGGAGGGCGCGGGCAAGCGCGTCGACATCGCGGCGGTGGCCCTCACGGCGGGCATGACGGTCGAGCAGATGACGGCCCTGGACCTGGGGTACGCCCCGCCGTTCTCCCCCGTGTGGGACCCGGTGCTGGTGGCGGCCCGCAAGGCGGCGGCGAAGGTGCGTGAGGCCGGGGTGTGATCCCGGTCCGCGGAGTTCACCGGTTCGTCCGCCGGACTGCGGGCACATGTCCCTCGTGGTCATTCCCGTTCATGACGTGAACCCGGTGCGCGGCACCCCCTGGGTGACGTATGCGCTGATCGTCGCGAACATCCTGGTGTTCGTGTTCACGCCCGGCATGGCCGGCTCCCTGACGGGGGACGGCAGCCTGGCCCAGCTCTGCCATCTCCAGGCGTTCCTCGACCGGTACGCGGCGGTGCCGCAGGAGCTGATCCACCACGAGATGCCGCGCCTGGTGCCCACCGGCGAGGTCGGGGTGGGCCCGCAGGGAGCGGGCTGTGTGATCGCGCCGCCCGGCTACGGCAAGTCGCCCGAGCTGAGCGTCCTGACGGCGATGTTCCTGCACGGGAGCTGGCTGCACCTGCTGGGCAACATGCTGTTCCTGTGGATCTTCGGTAACAACATCGAGGAGCGGATGGGGCACCTGCGGTTCCTGCTGTTCTACGGTGTGTGCGGCTACGCGGCGTCCTACGGCTTCGCCCTGGCGAACTCCGACTCCGGGGACCCGCTGATCGGCGCCTCCGGGGCGATCGCCGGTGTCCTCGGCGCGTATCTGGTGCTGTACCCGAAGGCCCGCGTCTGGGTGCTCGTCCCCTTCCTGATCTTCCTGCCGCTGCGGCTGCCCGCCTGGATCGTGCTGGGCCTGTGGTTCGTCCTCCAGGCGTTCTACTCCGCCGGCCAGGGCGTCTCCGACGCCGGTACGGTCGCCTACGTGGCCCATGTGGTCGGCTTCGTCGCCGGCCTGCTCCTGGCCTGGCCCCTCAAGCCCGGCACTCCCCCGCCGCCGCAGCCGCGCGGCGCCCTGTTCGGCCGCCGGGCTCGATGAGGTCCCGCCGAACACATCCACGGCGACCACGAACAGCCGGCCGGAGTCGTCCGGAACCCACGCCGGACTCGTGGGCGTGGACCGCGAAGTGGCCCGTTGCGATGCGTACGGCGTCGAAGCCCGGACTCGATCGGACAAGAGCTCGCGACCGTCCCGGTCATGGTGGCGGACACCCGGCCGGGGGCGTCGGCACTCGGTCTGCCCGGTGCGGCGGCATGCGGACCGGCTGCGGAAACGCCACCGGGTACCAGTGGGACGCGCTCTGTAGACGTCGCGGAGTTCCGAGCCGGAAGCACCTGCGTGGAGCGCCTCCCCCGCCATAGGTGCCCGATGAACGGACACCGATGGCTGGATAACGGTCTTGTCTCGCCCGCTGGGACTTTGCCGAATTACCTATAGTTATGTGATCTACATCACTAAAGATCTAGTAAAGGTCGTGGTAGAACTGCGCAACTCCGCAGGTGGCACCACCCCTCGCCGCAGTGCGGAAGGTCGGCACACACGTCGACTGCACGACCAGGGTGATCACGGTCCGAGTTCACGGACCGGTTTCCCAGGGTCGCCGATCGGACAACGGTGTTCGCTCAGAGACCGCACATCTTCCCCACGCATCTCCCGCGTCGGTACTGCGCCATCGAGGTAGCCACAGTGTCACTCGACTCCATCACCACGTCCGTCGACAAAGCCGTCAGCGGATTCTTCGAGCCCATAGCCACCTGGCTCGTAGAGGTCATCTTCTACGCCGTTCCCGTCGGAGGTACGGACCTTCCGCTCATCGTCGCCTGGCTGGTGGTCGCCGGTCTGGTGTTCACGGGCTGGTTCGGGTTCGTCCAGCTCCGCAAGTTCAAGCTGGCCGTCGACGTGGTGAGAGGGAAGTACGACGAGAAGGGGGCGGCCGGTGAGGTCAACCACTTCCAGGCCCTGACCGCGGCCGTCTCCGGCACGGTCGGTCTCGGCAACATCGCCGGTGTGGCCGTCGCCGTGTCCATCGGCGGCCCCGGCGCCACCTTCTGGATGATCCTCTGCGGCCTGCTCGGCATGGCCACCAAGTTCGTCGAGGTCACGCTCGGCGTGAAATATCGTGAGGTGCACGCCGACGGCACCGTCTCCGGCGGCCCCATGCACTACCTGCCCAAGGGCCTGGCGGAGCGTTTCGGCAAGAACGGCAAGACCCTCGGCAAGATCCTCGCGGTCCTCGCGTCCTTCTTCGTGCTGTTCTTCGGTCTCTTCGGAGGCAACCTCTTCCAGGTCAACCAGTCCTACGCGCAGCTGGTCTCCGTCACCGGCGGCGAGGACGGCCTGACGGGCTCCTCCGCCGGCGCCCTGTTCTTCGGCATCCTCATCGCCTCACTCGTCGGCATCGTGCTGCTCGGCGGCATCCGCTCCATCGCCAACGTCACCAGCAAGCTCGTCCCGGCCATGGCCGGCATCTACATCGCCGCCTGCCTGGTCGTGATCCTGGTCCACGTCACCTCGGTGCCGGCCGCCATCGTCACCATCATCGAGGGCGCCTTCAACCCGCAGGGTGTCGCCGGTGGTGTGCTGGGAGCGTTGATCATCGGCTTCAAGCGTGCCGCGTTCTCCAACGAGGCCGGCCTCGGCTCCGCCCCGATCGCGCACTCCGCGGTCAAGACCAAGCACCCCGCCAGCGAGGGCCTGGTCGCGCTCCTCGAACCCTTCATCGACACCGTCGTCATCTGCACGATGACCGCCCTCACCATCGTCATCGCCAACCCCGCCAGCTGGGGCGAGGCCCGCAAGGGCGAGTCCATCGGCGGCGTCACCATCACCTCGGACGCCTTCGCCACCGTGATGCCGTGGTTCCCGTACATCCTCACCGTCGCGGTGCTGCTCTTCGCCATCTCCACGGTGCTGACCTGGGGCTACTACGGCCTGAAGGCGTGGACCCACCTCTTCGGCCGCAGCCGCACGAGCGAGCTCGTCTACAAGGTCGTCTACACCCTGTTCGCGATCGCCGGTTCGCTGCTGACGCTGCAGACGCTGATCGACATGGCCGACGCCGTGCTCTTCATGCTCGCCGTCATCAACATCATCGGCCTGTACCTCCTCGCCCCCGTCGTCAAGCGTGAGCTGAACTCCTTCCTGGAGTTCGTCCGCACCCGCAACGCCGGTGAGATCACCGAGGACGACAAGGACCAGGAGTCGGTGAAGACCACCGTCTGACCGTCCCCCCCGGCGGCCCGGCTCCTTGAGCGGGCTCGTGCACACCTCGCGCCTCGGTGTGGACGGGCCCGCTCGTACTGACACGTCCGCCCGGACGGAAGCGGGCTCAGGCCACTCGGGCGCTGCCCACCGGTCGGGAGGCAGCTCGGTCCGGCGCCGGCACGGGCAGGATCATATGACCGGGTGCCTCGAAGGGCCACGGGACACCCCGGTCTCGGCCCGGGCTCGGCTCGCCCCCCATGTCCTCGTAGCCGGTCAGGGACGCTCGCTGCCGTCGAGACCTGGCGCGCAAAGACCTCGGGTCCGGCAGCAGACGGGGCCCCGGGTCAGATCTCGTTGCCGGGCCAGCCCAGCAGTCTGGCCCCGATGACGGCGGTCTGCAGGGTGTAACGGTGGACGGGGTCGGCCGGGTTGGTGCCGGTGAGTTGGTGGATGCGTTCCAGGCGGTAGGTCAGGGCCCGCACGCTCAGGCGCAGGCGGCGTGCCGCCTCGGCTGCGACGCATCCGGAGTCGAAGTAGGCGGTGAGGGTGTCGAGGAGGGGCTGGGCGCCGCCGCGTGCGGCCTGGAGCGGGCCCAGGGCGCTGCGTACGAGGTCGGCCATGGCCTGCCGGTCGCGGGTGAGCACCGGGTAGACGAGCAGGTCCGCGGAGCGCAGCACGGGCTCCTCCAGCTCCAGGCGGTCCGCCAGGTCCAGGGCGTTCAGGGCCTCCTCGTAGGAGTGGACGACCCCGCCGGCGCCGGGATGGGCGCGGCCGAGGGCGACCCGGCCGCCGTCGGTTGCCGCGTGCGCCTGCTTGGCGAAGAACGCGAGCACGTCGCCCTGGTCACCGGGTGCGATGCAGACCAGACGGCCGTCCTTGGTGGTGAGCAGGATGCGGCGCTCGCCGAAGCGGGCGACCAGGGCGCTCTCCACCTGCCGGGTCGCCGGGTGGGTGTCATCGACCGGCGTGGCGCCTTGGGCGACGGCGACCGCGTGGGCGCGGGAGAAGAGCAGGCCGAAGCGTTCGGCACGCTCGGCCAGGCGTCCCAGGTCGCTGCGGCCGTAGAGCAGGTCGTCGATGAACTCCCGCCGCGCGGCCTCCTCCTGCCGTACGGCGAGTTTCTGGGACCGTTCGTAGCCTTCGGCGAAGGCGTCCACCGCCTGCTCCACGGCGGCGAGCACACGGTCGGCCCCCGCGGGCGACAGGGCGGGCGAGAGTTCGCGGGCCGCCGCCAGATGCCGACGGACGAGAAGACGCAGTCCCAGGCCCGCTTCCGCGGCGCGTTCTCCCCGGGTGCGCAGGGACTCCAGCTCGTTCCGGGTGAGGCGGCGGCCCGTGGCACAGACGCCGGCCAGGATTTCGGCGTAGCCCTCCAGATACTCGTCGGGTATCGCCGACCGCGTCACGCGTCCTCCTCGATGGTGATGTTCGCCGGCCTTTCCCAGGCACGGCGGAACAGAGTGACAGATGTCCGGTCGAGCCGGCTGCGCACCTCATCCGCTTCCGCCCGCTCACGGCCGGCGTCATCGGCTGCCGGGAAGGGCAGCGTCGTCTGCCGCGTCCAGGGTGGGCCCCGCGGCTCGATGCCGCGCGGGCCCTTGTGCCGACTGCCTGCTCTCAGCCGATCTGGATCTTTCCGTCGGCCTCGGCAGCCGACGGATCCGCGGGCTGGACGTCACCGTTGCGCCGGGTGATGCCCTTCAGCAACTCGGCGAGGTCGACGCCGGTGGTGGAACCGAGGAGTTCCATGCCCTGGGCGACGTTGTCGGCGACGGTGCGCGACAGCCGGCTCGCCCCGTCGGTGGAGATGACGGTCATCTTGTCGACGGCGCTGAGCGGTTCGGACGCCTTGGCGACGACCTGCGGCAGCACCTCGACGAGCATCTGCAGCACGGCCGCGTCGCCGTACCGGGCGAAGGCGTCGGCCTTCTTCTCCATCGCCTCGGCCTCGGCCGCGCCCCTGGCGCCGATCGCCGCCGCCTCCGCCTCGCCCTCCAACCGGACCGCCTCGGCGATCGCCGCGCGCCGGGCCCGCTCGGCCTCACCCTGCTTGAGCCCCTCGATCGCCTGCGCTTCGGCCAGCGCGGACCTGCGCTGCTTCTCGCCCTCACCCGTGAGCCGGGACCGCTCGGCCTCCGCCTGCGCGGCGGCGATCTCCGCCAGCCGCTCGGCCTCCGCCTGCTTGACCCGGGCGACCCGCTTGGCCTCGGCCTCCTGCTCCGCGGCGTACCGCTGGGCGTCGGCCGGCTTGCGCACCTGGGTGTCGAGCTGGCGGTCGGTCAGCGCGGCCTGCCGCTCGGCGACCTTTTCCTGCTCGGTGAGGATCTCCTGCTGCCGGGCGGCCTCGGCCAGCGGGCCGGCGGCGTTGGCGCGGGCGGCCGCCTGGTCGGTTTCGGCCTTGATCTCGGCCTGCCTCAGGTAGAGGGTCCGCTGGGCGACCGCGATCTCCTCCTCGGCCTTCAGCCTCGCCTGCTCGGCGGCCCGCCGCGCCTCCGCCTCGGCGATGTCGGCCTCCTGCTTGGCGCGGGCGGCCTCCGGGCGGCCGAGGTCCTCCAGGTAGGAGCCCTCGGTGGTGATGTCCTGGATCTGGAAGGCGTCCAGCACCAGGCCCTGCCCTGACAGGCTGGCCTCGGCCTCCTCGGCGACCTGCCCGGCGAACGCGGCCCGGTCGCGGATGATGTCCTCCACCGCCATCCTGCCCACGATCGCCCTGAGCGCGCCGGAGAGCACCTCCTGGGTGAAGCCGACGATGCCGTCCTGCTGCATCAGGAACCGCTGGGCGGCGGCCCGGATGGCGTCCTCGGTGCCGCCGACCTTGACGATGGCGACGCCCTCCAGATTGGCCTTCACCCCGCGCAGGGTGACCGCACCGCGTACGGCGACCGGGATGTGCCGGGAGGACAGGTCGAGGGCGAACTTCTGCTGCACGAACGGCACGACGAACACACCGCCGCCGACCACGACCTTCTGCCCGCTGTTGTCGGTGAACACCCGGCCGGTCTCCGGGTCGGTGGCCTTCTTGCCGCGCCGTCCGGTGACGATGAACGCCTCGCTGGGGCCGGCCACCTTGTACCGGCTGACGACGACCAGCGCGATCAGTACGAGGAGTACGACGACTCCTCCCATCGCGATGACGACAGAACTCATGGTGTTGTCCCCTCAGCCCTCCCTGAGGACGGCGATCGGCGAAGGATGCGGGTAGGTGGACCGGCACCGCGGAAGTGATGCCGGAAGCGGGTGGGTGGTTTCGAGTCAGCGTTCGACGGGGCGGACGGACACCGCCGACTGCGACAGCGTCTGCTCGACCCAGACCTCGGCTCCCCGGGCCACGGCGACCGGGCTCTTCGCCGCGAGCTTCACCGGCTGTCCGGCCAGGCGCACCAGCACCTCGCCGTAGCCGTCGGCGGGGATCGCGGTCACCACCGAGCCGGACACGCCGATCAGGTCGTCGTCACGCGGAGCGGCACCGGAGTAATCACGCATCAGAGCCCGGCTGAGGCGGTAGGCGAACCAGCCGGTGAGGACACCGGCGGGCACCCCGATCACCGTGGCCCCCACCGCGCCCAGTCCGGTCGTCCCCAGGACGATGGCCCCGGAGAAACCGAGCACGGACAGGAACCCGGCGATCACCGGCAGCGACAGGAGTCCGTCGAGCAGGCCGTCCACGACGGAGATCCCGTCGAGCAGCCCCTCCAGCACGCCCTCGAGGACGAACGACAGGACAAGGAGGACGACCCCCGCAATGCCGAGCCCCAGAAACCAGGCCATCCGCGCACACCGCCTCTCCTTGCCCTCCCCCGCTGGTGGACGCATCGTCACACGCGGACTCCTGCCGGGACATTGCCTGATCCCGGCAATCTTTACGTGCTTTTAATGCCGCACCCCGCACAGTCGGGCGGCCGACGGCCGCAGTTCCTGCCGGTGCTCTGTAACACCGGGACAGAGAGCTGTACCGTCCCCAGCGGTGTGCCGGGAAGTCTGGTCGGCGATCTTGATGGAAGAAGCCGGAGAGCTTCGCCGAACGGGGGTTCCGACGTGGTGCTCATGATGGTCCTCAGAGTGGTCCCGGACGTAGCACACGCACCCGCAGGGATACTTCTCCGCCTCAGCGGGGGGTGCCGTACAGCATGATCAGGTGCTCTCAGCCCGCGCCTGGCGTGCCGCGTCCGGGCCACATGATCGTGTGCGGGGACGACGCGCTCGCCGAACGGCTGGCCGCCGAACTCGCCACGGTGTACCGGGAGCAGGTCACTCTCGTCGTACCGCCCTCGAGGCGCCCCGACGCCACCACCGGAAGGGCGCGTGCCGCCGCGCTGCTCGGCTGGATACAGACCGCCATGAACCGCACCGAGGGACCGAACGGCTCCAGCCTCACCGGCAGGGTCCGCCTCCTCGAGGCCGCCGTCCTCGACGAAGCCGCCCTGTCCGGGATGGGCGCGCGCGAGGCCGCCGCGCTGGCACTCGTGCATGACGACGATGAAACCAACATCCACGCCGCGCTGGCCGCCCGCCGTCTCAACCCGCGGCTGCGCCTGGTCATCCGGCTCTACAACCGCAAGCTCGGCCAGCATCTGGAGGAACTGCTCGACCAAGCCGCCGCCCTCGCCGTCCCCGGCCTGGACCCCGAAGCACTGGACACCTCCACCACCGTCCTGTCCGACGCCGACACCGCGGCACCCGCCCTCGCCGCCACCGCTGTGGCGGGCACCAGCAAGATCGTCCAGGCCGGCGGGCTGCTGCTCCGTGCCGTGGAACGCACTCCGCCCGGCCACGGCCGGATCGCCGCTCCCGGCCTGTGCACCCTCGCCGTGCTGTCGTCGACCACGAACGACCCGGCCGGATCGGAAGGTTCGGACGCCAGCGGCCGGGAGGCGCCGATTCTGCTCCCGGACGACGACACGGTCACCGCCGCCACCGGGCGCGGCACCGTGGTCCTCGAAACCGTCACGCACACCGCCTCCCGTATCGCGCAGCGACGCCTGGCGAGGCGCGGACTGCCGCTGGGTTCCCTGTTCTCGCGCCGGCTGCGCTGGTCGCTGGCCGGTCTCCTGGGTTGCGTCCTGGGCATGGCTGTCGCGACCTGGCTGACCACCGACGAGCATCCGTTGCACGCCGCCTACCTCACCCTGCTCGACCTCTTCGCGATCGGCGACCCCGCGCTCGACGGGCCCGCCGCGCGGCAGGTGCTGCAGCTCCTCGCCGGCCTCGCCGGCCTTCTGCTCCTGCCCGTTCTGCTGGCGGCCGTACTGGAGGCGCTCGGCACGTTCCGCACCGCCTCCGCGTTGCGCCGGCCTCCCCGCGGCCTGTCCGGCCACGTCGTCCTGCTCGGCCTCGGCAAGGTCGGCACCCGGGTGCTGGCCCGGCTCCGAGAACTCGACATCCCCGTGGTGTGCGTGGAAGAGGAGCCGGAAGCGCGAGGCATTCCGCTCGCCCGCCGCCTGCGCGTCCCCACTGTCCTCGGGGACGCCACCCAGGAAGGGGTGCTGGAGGCCGCCAAAATCCACCGCGCGCACTCCCTGCTGGCCCTCACCAGCCACGACACCACCAGCCTGGAAGCCGCTCTGTACGCACGCTCCGTCAAACCGAACCTGAGGGTGGCCCTGCGCCTGTACGACGACGCCTTCGCCACCGCCGTCTACCGCACCCTGCGCGCCGCCCACCCGCGCGCCCTGACCCGCAGCCGAAGCGTCTCCAGCCTCTCGGCGCCCGCCTTCGCCGGAGCCATGATGGGCCGACAGGTTCTCGGCGCCATACCCGTCGAACGCCGCGTGCTGCTCTTCGCCGCCCTCAATGTCGCCGGGCACCCGCGGTTGGAAGGGCGCACCATCGCCGAGTCGTTCCGCCCAGGCAAGTGGCGCGTTCTGGCGCTGGACACGGCCGAACCGGACGAGCGGCTGCCGGACCTCGCCGCCACACCGGCGAACCACGGCGTCGAACGTCCCGGCGGACTCGTATGGGACCTGCACCCCGGCTACGTCCTGCGGCCCGAAGACCGAGTGGTACTCGCCGCGACGCGCCAGGGCCTGGCCGAACTCCTCGGCCGACAGCCGTGGCTGGGGACACGAACCGCTGACGCCTAGGTGTGCTGTTCGGGCCGCGGCGCCCGGGACGTTTCCTGGACCCATCCCAACCTTTGACGGGAGCGTGCCCCCGGACGACTCGGAGTTCTGGAGCGGGTGGCTGCCGCTGGTGGAGCGGACCATCGCCTGCGGCGTGAAGGTCTGCCGGGCCCGGATCGCGCCGCGCTCCCGTGTGAATTGCATGCGCTCCCGTGTGAAGTGCGCGCCCATTGATGTCCCGGCACACCCCCTGGACGAGGCCGCGTTCCTGTCGAACAGTGGCGAATGCCGGCCGAACGGCGTCATGCCGGCGCGGCGCACCCTTCCTGCACTCGGCTCAACGTGTCATGCCTGCCCGCAGCGCACCGCTCACAGCTGTCCACGTGCTACCCGAGAGGTCTCGATTCAGATGCAACGTACCCGCAGTCTCCACAGATCAGGTCCTCGCACCCTTCTCACCAGCGTGGTGGCGCTGCTGTCTCTGCTGACAGCACTGTTGATCCCCCTCTCAACGGCCGCGTCTGCGAGGGCCACCGAGTCGGGCTCTCTGCCTATGGTGACCTGCACAGGCAGTGCTACACAGCACTACTCCCCCGCCCTCGTCGCGGCCACGCGACTCACCACCGTGACCTCCACTCAGAACTACGGCACCTGCGTGGACGTACAGGTCGACCCCGACGGGCCACCCGTCACGTCGGCCTCCAGCTTCGTCACCTTCACCGCTCCCCTCAGTTGCCTGCTCTCCCCGCCGGTGCTCGAAGTGGAGCTGATCATCCACTGGAACGGGGGCCGCACCAGCACCGCACAGGCCCTGGCGGTGGTCAGCCGAACCACCGGCACCACCATCGCGACCGACACCGGCACCATCACCTCGGGCCTGTTCGCAGGCAAAACGATCAACGTCACCGTTGTCTACCCGACGCTGGACGTGACCGGATGCCTTCTCGGCGATGGAGTGTCCGAGATATCCGGGGCCGCCACCCTCGTCGTCGCCCCGGTCTGACCTCGGCAACCCGCCTTGGCCACCGTCCTGGTCGGGCGGTGGTCGGAGTGCTCAGCGTCGGCTCCGGCAGCGTCCCCATCACACCGGACCCTTCCCACCGATCACCGGGCTGCCTCCGACGACCGGTCCCCGGCCGACTGACTGACGGTGTCCTCGATCCACGCCGCGGCCGCATCACGTCGTGGCCGCGGCTGGGCTGCCGAGTTGTGCCCTCGCCGGATCAGCCGAACGCGGCGAGGCGACCGGCCGGCACACGCGGCCGATCCGTCGCGGCCCGTGGCATCAGCGGAGTGAGCAACTCCCACTCGTGATCGGTGGCAACGGGGCCAAGGGGCCCGAACGCCTCGCCCTGATCCGCCTCGGCACCATCCAGGCGTCCGGCTCACGCGGCGTCCTGCTGTGTTGCCCAGCGCCGCCCGCGGCTCCGCCGCCCCCGACCGGCTCACCTCATGGCTTACCCCGGCATGAGGCCATGGCTGTGGCGGCGTACGAACTCGTCGGTGCGCTGGGCTTCGATGCCCTAGGTGACGTGGAGCGGTCCAAAAGCGACTCGTCCGCCTCACCACGTAGGACACGGTCTCGAAATCCGGCCGCACCGGCCACGGCGGCTCGAAGAGAGGTCCCGCCCGTGACAGTGGCGCACCGGTCGGCTCAGGTGCGGGCCGGTTCCTGCCCGGCCGGGGTCTTGGCGGCCGCGGAGTCACCCGTGCCGGTTCGCCCGGCGGGGATCAGCAGCGCGACGGCGGCAGCGGCCACGGCCACGCCGCAGCCGATCAGCAGCCCGGTGCGGAAACCGTCCTCGGAGGCGAGGGTGTGGCCGCCCATGGTGATGGTCATCTGCGCCAGGACGACACCGATCACCGCCGACCCGATGGTCGTGCCGAGCGAGCGCATCAGGGTGTTGAAGCCGTTGGCCGCGGCCGTCTCGGAGACCGGCACAGCGCTCATGATCAGGGCGGGCATCGCACCGTAGGCGAGGCCGACGCCGCTGTTGATGACGATGCCGACGAGCATCAGGCCCCAGGCGGTCCCCATGAGCGGGAGCGCGATCCCGTATCCCACGGCGATGACCAGTGCGCCGCAGATGAGGGTGAACTTGGGCCCACGGGCGTTGATCAGCTTCCCGCCGAGCGGGGAGACGATCATCATCATCACACCGCCGGGCGCGAGGTACAGGCCGGCGGCCAGCATCGACTGGCCCAGGCCGTAGCCGGTGGCCTCGGGGAACTGGAGGAGCTGCGGCGCGATCAGCATGAAGGCGTACATGCCGACGCCGATGAGGATCGAGGACGCGTTGGTGAAGAGCACGCGGGGCCGGGCGGTGGTGCGCAGGTCGACCAGGGGTTCCCGGGTGCGCAGCTCGTAGAGGCCCCAGACGGCGAGGGAGACGACGGCCAGGGCGAAGAGGCCCAGGACGGTGCCGGAGGTCCAGCCCCAGTCGCCGCCCTTGGAGATCGCCAGCAGCAGCGAGACGAGGCCGATGGCGAGACCGACGGCGCCGGGGGCGTCGAAGCGCTGTCCCTTGGCACCGGCCGGCACGTCGGGGACGAAGAAGAAGATCAGGGTGCCGACCGACAGGGCGAGCACGGCCGCCCCCCAGAACAGCACACGCCAGTCGGCGTACTGCGCCACGGCCGCGGCCAGGGGGAGGCCGATCGCGCCGCCGATGCCCATGGAGGCGCTGACCAGGGCGATGGAGCCGCTCAGCCTCTCCTGCGGGACGACATCGCGCAGCAGCGCGATCCCCAGGGGGACCATGCCCATGCCCATGCCCTGCAGACCGCGGCCGATGATCATCGGCACGACGGACGAGGCCAGCGCGCACACCACCGAGCCCACCACCAGCGGGACGGCACAGACGAGCAGCATCCGCCGCTTGCCCAACAGATCGCCGAGACGCCCCGAGACCGGGACGCACACGCCCGCGACGAGCAGCGTGACCGTGACCACCCAGGCCGCGTTCGAGGGGGTGGTGTCCAGGATCTGCGGCATCTCCGCGATCAGCGGGGTCACCAGGGTCTGCATGATCGCGGCCACGGTGCCCGCGAGCGCGAGCGTAGCGACGACAGCGCCTGAGCGGGTGGTCGGCTGGGGGCCGTCCATGGTGGGGCTCCTCTATGGCAGTCAATGAGAACGCGGCACCCTGCCGACGCGTTGTGCATCATACATATGATGTGTATCTAACACATGACATGCCTGATGCATATGATGGCCATGGGGGAGCTCCAAGGAGTCGCACCGCAGAGAAGAGGGCACGTGAACACCGCGGACAGGTCCACGGCTCAGGTCGAGTTCGAACAGATGCTGTTGAGCCGCTACATGCATCTGCACAAGAGCAAGGGGCGCCGCGCCGACAGTGCCCTGGACCGCAGCGCCTACATCCTGCTCAGCCGGATCCGCGCGCAGGGCCCGATGTCGATCGGTCAACTGGGCGACGCCTTCGGACTGGATGCCTCCACCCTCAACCGGCAGACCGCGGCCGCCATGCGCGCCGGCCTGGTCGAGCGCATTCCCGACCCGGAGGGCGGCATGGCCCGCAAGTTCCGCATCACCGACGAAGGCGAACGGCGCCTCGACGAGGAACGCGCGGGCCTGGTCGCCAGCCTGGACCGCATCATGGCCGACTGGCCGGAGGAGGACATCGCGGCCTTCGCCGGCTACCTCCGGCGTTTCAACTCCGACATCGAGCGCCTCCACGGGATGCCCTGGCCGCGCGCGTGCGTGAATCCGTAGCCGCCGAGACCGACGCCGGGTGCGCCGCAGGTGAACCGACGGCCGGGTGTGCCGTAGGTGAGAGGTGGTCACGGCGCCTGGCCGCGCGCGGGGCGCCGGGCCGTGCCGGCATGGGGAGGTGGGGGTGGCAGGAGGTGTGCCATGCCACGGACCACTCAGCCGCCGCCGGACGACTTCGCCCACTCGGGCGAACTGTTCTCCTCGGTCCGCACGTACGCACGGTCGTCCGGCTTGCCGAACCAGAGCTGTACCCAGGCCGCCCTGCACTGCGCGCTGTACCGCAGCCGGACGATGCGTCCCTCGTGTGCGGCGTCGTCGATCGTGACGGCGTCGTCGACGCAGTGGGTCTCGATCGGATCGAGCCCGTGGCAGGACGTGGCGTAGCACGTCGGCGTCGCTTGCGTGGGCGCCTTCGGCGCGGCCTCGGGAGCGGCCTGCGCGGGGTGGGAGAAGGTCGAGGTGGCCGCCGCTGCGATCAGGACCGCGGCGAGTGCCCCGCCGGGACGGCGATTGCTCATCATGACGGTTCCTTCCGGCGATACGTCGTGCACGGGCCCCCGCACCCGCCATTCCAGCAGTTGAACGCATCGGGCCGCGCGCATACCCGCGAGGGCACGACGCCGTCGGCCCGGGTACGTCCGATCGCCTCGTGGTGCGCGCCGCAGGGGCGTGCCCCAGGGTGACGGCGGAGGGCAGGCGCAGACAGGCGCGGGCGGACAAGGTGCCGGTCGTGGGCGGGAGTTCCGCGGTCGGTGGCGGGCGCTGCGCGGAATCGCGTACCTGCGGTCTTCCTGCCGGGCGGCGGAACGCACTCAGTGGCCGTGCGGGCACCCGCCCTGCCCTCGCGTACCTGGAATCCCCGCCGATCGACCGTGTAGACAGGGCATCTGACACCCCCTGTGCCGCAGGAGCAGTTCTTGAGCGATCACCAGGCCCTGAGAGAGACCGGCAGGACCGGTCGAGACCGCGCGCCCGCCCGGAAGGCCGCGGTCGCGCCGCGTGAGCGGCCCGCGGGACTGCTCGCCCTTCAGGCCGCGGCCGGGAACGCCGCCGTCGTCCAGAGGCTGCGCCGGGCCGGGCACCTCGACGGCCGGGACCAGGACCCGCACGGCCCCGGACAGGGCGAACAGGCGGCACCCGCCGTACAGCGCTCCACCGTGCACGACGTGCTGCGGGCGCCCGGCAGGCCGCTGGACGAGACGACCCGGGCCGACATGGAGGCCCGCCTGGGGGCGGACTTCTCCGACGTCCGTGTCCACACCGACGCCGCCGCCAGGGCTTCCGCCGCCGAGATCGGCGCCCGGGCCTACACCTCGGGCAATCACGTCGTCCTCGGTGCCGGGGGCGGTGACGCGCACACCCTCGCCCACGAACTCACCCACGTCATCCAGCAGCGGCGGGGCCCCGTCGCCGGCACCGACCACGGCGGTGGGTTCAGGGTCTCCGATCCCTCGGACCGTTTCGAACGCGATGCCGAGGCGACCGCGCGCCGGGTTCTGTCGGGACCGTCCCCGTCGCACGGGCCGTCTCCGTCGCACGGGCAGGAGACGACCGCCGGCCCGGCGTCCGGGGCGCCGGTGCAGCGCGCGGCGGCGAGCGGGTCCGGCCTTCCGGTGATCCAGCGGTGGACGGACGGCACCATGTCGGGCGACGACCCGGTGTTCCAGGCGGACAACGGGCGTGCCGGGAGCGTGGAGGTGCACAACCTGCACGGACGACCGCTGGGCGCGGCCGCCAACTCCCCCTCCGTCGAGCCGGTCGGCTGGGCCCAGCTCAGGCAGGAGGGCTACACCAAGATGGCACCAGGGGGTGAGAAGCCGGTCGGCGCGCCCTACCGTGCCGTGCGCATGCACCTGTTCAACGGGCGGCTCGGCGGCCCCGGTCACAATGTGCTGAACCTCGCTCCCGGCCCGGGAAAGCTCAACTCCCAGATGTCGGCGCAGGCCGAGGACCCGGCGAAACTCCTGGTGGAGCTGGGCCACAAGGTGTGGCTGAGGACCACGGTCCGCTACCAGGACAACAACACCAACGGGGCCAACTTCGCGTCGGTCGTCCCGAACCACATCACGATGGAATGGGGCGTCGAGGGCGATCCGGCCTCCGCCCGGCAATGGTCCTCCTCGATCAACCTGCCCGTCGACCCCCTCAGCGCCGCTCAGGTCGCCGTGTACAGCACCTATGCCGGCACGGCCGGTCAGCTGGTCCAGGAGATGGGGGCGGCGAACGTCAGCGACCAGATGCGCGCCCAGGTGCTCGGGCTCGTACCGAACGACCAGCTCAAGCTGGCGTTGCTGAACAACTTCCCCGCTCTCTACCGAGGTGCGGAGGGCGCCGACCAGGCCCGTTACATCATGCTGTACCCGACCGCGGCGGACCGGGTGGCGTTCCTGGGGCGCGTGGGCGTCACCGCGCAGGAGCTCTTCCCGCAGGCTCTCCAGCCGCTGTACCGGGCCGGGGCCCAGGCGGCGGCCGAGGGCGTGTTCCGCGCCTGGGGCCTGAGCGACGACGAACAACGGCAGATGGTCTTCCACTACGGGGAGGAACTGCTCCAGGCCATCGGCATGGCCGGCGTAGAACTGGTCGAGCGCCTGGGCGACAGGGGATACGCACTCGTCAAGTACTACTCCGAGCCCGATCAGATGATCCTTCTCGACACCCTGGAGAGCCGGGGCACGCTCGGCGCGCTGCTGCAGTCCGCGAACTCGCCGGCCGTGCGCAACGCGTTGCTGGACCAGTGGGCCGTGCACCGGGGCAACGCCTCCTCGGACGCCAAGACGAGATTCATCGACGCGACCGGCATCGGCCAGGCGCACAAGACGGCGTACCGGAACTGGCGCAACAGCCAGGACAGGTCCATCGAATACCGGGACAACCGTCCCAGGCGGGCGGCCGCCGGTGCCAACCGGTGACGACAGGACAGGAGCACGCATGACGGCCGGTTACCGGCGGCGGATCGCCGAACGCGTGGCGCGCTTGGGCGCCACACCCGGGTTCTCGGTGCGCGCCTACGAGGTCGCGCCGCCCGTCACGGACGCCGAGCTGGCCTCGGTCACCGCCTCCGCACAGGGGCGTCTTCCGGTCGGGGTGGCCGAGTTCTACGGCGAGCTGAACGGGTTCCGTCTGGAGTGGGAGTACACCGCCCCCGAAGGCGGCGGGCCCCCCACGGACTTCGGCTCGGTCAATGTCCGGCCCCTCGCGGACGTCTTCGCGGAGGGGCTGGGCGACACCTGGTACGACGACTTCGAGGGCGGCGACCGCTTCCGGGCGGTCAAGCCCTTCGACGTCTACGCGCCCGAAGCATGCGCGGCCTTCCTCCAGGAGCCCGGCGGCGCTCCCCGGGACGACGTCCACTTCCACTACTTCGGCGAGTCCCTGAGCCCGCTGCACCTCACCTTCCCCCAGTACCTGGAAGGTGCCCTCGCCTCCTGCGGCTACGTCGACTGGCGCATGGCGCTCACCCCCGACGATCCGGGACTGCCCGCGGCCCGGCGGACCCTGGAGCGCATGCGGGCGATCATCCCCGGGTTCGACGGGCTGCCCCGGCCCGGTTCCGCGTAGGCCGCCGGCGACCCGGGGGTGGACGGTGGCGACCTGGAGCCCGGGAGCGGGCTCCAGGTCGCCACGCCGGTCGCGGGTCAGGAGCGCTGGAAGAACTCCACCTCCGCCAGGGCCAGATGACGGCCCGGGGCGAGACCCGTGGGCGAACGCAGCACCAGACGCACCGTCTTCACGTCGCTGATGCCGGTGGGAACCGGCTGCGGACCGGGCTTGTCACCGAGGGTCAGCTTCTTGGTGTGCCGTGTGCCGTCCTGGGTGGTCACCTCCAGCTCCAGCTCCAGCGCGCGAGCCTGGCGGGCGTAGGGCTGGGCGGACGCGGACGCGCCGTTGGTGATGAGGAGGTCCACCAGCCGGAACGGCCTGCGGAAGGTGTACGTCACCGAGGCACCCTCGGCGGAGGCGCCCCAGTAGCGGTTGCTCAGCCCGTCGGTGGTGTTCCGCGCCGGGTGCCCGGGGACCTCGTCGCTCGCCTCCACGCTCACCGGCGTGATCGGCTTGGGCTTGCCCAGCTTGTCCCGGGTGTCCTCGATCAGGGCACGCCCGGCCGGCAGCAGCAGGAAACCTCCCGCGCACAGGGCCGCCACCACGGCCAGGATCACCAGGAGCCGGGCCACCCGGCCGGAGCTCGCGCGCGCCCGGCGGCGGAACGGCCACACGGTGCGCCACCACGGCAGGGGCGGGGGCTTCTCCTCGGGGTTCAGCACGGCGGCGCACCGCCGGCAGAACCGGCGGCCGGGCGGATTGGGCGTACCGCAGGCGGGACACGGCGTCCCCGCGACGTCGTCCGGCACGGCCACCGGCCGCACCGTCGGGCGTGGCGCCACCGGTCTGCCCGGGCGCACGGGCAGCACCGGACCCGGCGCCGACGCGTCGGCGGCGGGCGCCGAGGGTGGGCGGGGCGCGGGGTCGGACCGGGCGTCGCCGGGTGCGGCCGGGGTGACCGGGGCGACCGGAGCCGGGGGCTGCCCGGGGGGAGGGGCCGAGGACCGAGCCGGGCCGGGGGCCGGGCGCTCCCCCCGACCGGGCCGGCCGAGGGCCGGGGGCGTGCGCCTGCGGGCACGGCCGGTCTCCCGTCGTGCCGAGGCCGGGGCCTCCGGTTCCGGTCCCGCCGCCCGCTCCGGCTCCGTCTCCCGCTCCGGCCCCGCCGCCCGCTCCGACTCCGGCTGCGTTTCCGCATCGGTCCCCGGGGCCGTGTCCCCGGCGGAGTCCGGCCCGGCGGGGGCGGACCCGCGCCGGGCCGGTGGCCGCGCGGAGGCGCCCGGGGCGGCAGCGCTCTCCCCGGTCCGCCTCGCGCTCTCCGCGGCCTCCGGGGGCGGGCTTGGGGCCGGAGCGGCGTCCGGGGCCGGGACGGCCGCCGGGGTCGGGACGCTGCCCGCGGCCGCGGCACCCCGTGGCACCGGGCCGGTGACCGGGGCGGGGTCGCTGTCCGCGGCCGGGTCGGCCGGTGGCTCCGCGGCCCTCCCCGGCGCCGCGGCGGCACTCTCCGACCAGCCCAGATAGGCTCCGCAGTTGCCGCAGAAGTCGTCCTGCGGGTCGTTGGACGCCCCGCAGGCGGGACACGCGCGCATGACGTCACCTCCCTTCGCCGGCGGGCGGGCCGGGCAGGATCTCCACCCGGCAGACGGTGTGCACCGGGCACATGGCCCGGACGATCTCCCGGACCCGGTCCGGGTCGATCCGCTCCTCGCGGCCCGGCCACACCCGGACCAGGACCTCGGCGGCGGGCGCGGGCGGCAGCTCGGCACCGGGGGTGCCGGACCAGAGGGCCCCGCCGTCCCCGGTCACCTCGGCGTGCGCGCCGAGCGCCAGCCCGAGCGCCTCGACCAGTCCGCGCCGCGTGCCGCGCCACCGGTGCAGTTCCACCGCGCGGACGACGGCCTCGCGGCGTACCTCCATGGGCCACGCCCGGTCGTCGGTGGCGCCGACCCAGGACGCCAGCCAGGCCAGGAAGTCGGCCGGGGCCAGCCGGGGATCGAGGTAGGCGGGCAGGTTGTCGAGGGTGGAGAACACCGGAGCGAGGACGGTGTCGAGTCCGGCGGTGAACCGCTGGGCGAGGTCGTCCTCGGCGTAGAGGGCGGGCAGTTGCCCGCCGATCGGGTACCGGCTGGGAAGCCCGGGTACGGCGGCACGGCTCATCCCCGGTCCTCCGGCCCGGCGGCCGTGACGACCACCTGGTGCTGGTAGGAGAAGACCAGCGCGCCCGCACCCACGTCGATGCGGTCCGACGGAGCGCCGCGCCGCCCGGTGATCGGGTCGGCGGGGAAGAGCCGGATCTCCTCCACCAGCGCGTCCCCGGTGGCGCGTTGCACCACGCCGAACACCTCCCCGTACTGCACCGGCCGCCCGAACGGCCACCCGGTGCCCTCCGGGCCGCCGCGCAGCGGATCGAGGTAGCCGAACAGGGCGGCGAGCGCCGCCTCGCGCACCCGGTCGGCGTCGCCCGGCGCCGTCGTGAGGCGGGCCACCACCGTGACGCCCTGGTAGACCGGCGGCTCCACCACGAGGCGGGTGCCGATCAGGCGCCGCTCGTCCAGGCAGGAGGTGATCGCCTGGAGCACCCGGTCCGAGGGGATGAGCTGCTCGAAGCGGAGCCGGTCGCCCTCGTCGGGCACCGCGTCCGGCACCACCAGGACCCGTACCGCGCCGGGGCCGTCCGCGGCGGGCAGGCAGCGGACCCGGCGCACCGAGGGCGCCGCCTGGCGGCTGAGGATCTCGTAGTCCTCGGCGGTCACCGCGCGCTCCTGCATCCGCAGCGCCTCCGGGGCGCGCAGCTTGGCGTTGGCGACGGTTTCGCCGGCCACGCCGCCGCGCGCCGCCTCCCGGTTGGTGACCCGGGCGACGTACGGGACGGAGCTGCGCAGCACGGAGATGGCGCCGCGGGCGACATTGCCCGCGGGGCCGCCGCCGGTGCGGTAGCGGGCCACCCGCACCTGGGCGCCCTTGGGCGGCACCGCGCCGCACTGCCGCAGGGTGCCGTCCGGCTCGCGCAGCGCCGGGGGAAAGGCGAACTCCCCGGTGGTGGCGTCCACCCGGACGTGCCGGTCGGCGGGCCCGGAGCGGCCGAAGTGCTCCACCACGTCCCAGCGCTGCCACCCTTCGGCCGAGGAGACCTCCACCACGGGGGGCGCGCCGTCGAGGAGGACGGGCGGGCGGCCGACCCGGAACGTCTGGCCCGCGACCCCCTCGGAGGTGCCGAGCGGCACGTCGGTCACGGTCACCGCGTGCTCGGCGCACATGGTGCCGCCCACGGTGAACACCGACGCCTCGCGCACCGTCGGGGACTCCGAGTAGAACGGCTGGCCGGGCTCGGGTTCGGTGACGCGGCAGCGCAGCCAGCCGGCCCGGGTCCCGCCGATGACGGACGCGCGGTGCCCGGCCGGTACGTACACGATGACCTCGCCCGGCCGGTTCAGTCCGCCGGTGGTGTCCGGGCCCGTCTCGCACACCTGCCAGCCGCTGCCGTGCCACGCCTCCCACACGAGCGGGGGCTGGCGGGGGTCCACGCCGACGCCCTCCACCCGGCTGTCCAGCCGGACCGCGACGATGCACCGCGGCACGGCGGTGGGCAGGCCGAACAGCAGCGCGTCGCCCGGCTCCGGCGCCGCCTGGAAGCAGGGGATGTCGCGGCCCTCGGCGAGCGTGCGGGTCCGGTCGGTCTGCTCGCCGGCCCGGGGAGCGGTCACCAGCCGCGTCAACTCGCTGGGCGCGATGTGCAGTTCGTCCGTGGTGGTGAACACCACGGCGTCGTCGGTCTCGCCGCGCGTGGTGGTCACCTCGGTGCCCGCGGGCAGGACGACGGTGTCGGGCTGCGGCGCCGACAGCCAGAAGTCGACGTCGGCCGAGGCGGCGGCCGGCGGGAACAGGCGGATGCCCAGCAGGTCGAGGAAGGCGGTGTAGTTCTTGTCCGGCACCCGGTTCAGCCGGTACAGCAGTTGGTCCACGAGGTAGGCGAAGGTCTCGATCAGCGTGACGCCCGGGTCGGAGACGTTGTGGTCGGTCCACTCCGGTGCGCGCTGCTGGACGTACCGCTTGGCCTCGTCGACGAGTTCCTGGAACCGCCGGTCGTCCAGGTTGGGGGAGGGCAGGGCCATCAGGCGGCGCCCCGTTCCCCGCCGCCCTCGTCGGACGGGATCGTGTAGAAGGGGAAGACCAGATTGCGCCGGTCGTTGGTGGAGCGCACGGTGTAGTGGACGTCGATGTAGAGGGTGCCCGCCTCGACCGTGTCGTAGGCGACCACCACGTCGTCGACCGCGATGCGCGGCTCCCACCGCTCCAGGGCCTCGCGCACCTGCTGGGCGACCCGCCCGGCGGTGGCGCCGTCGCCGGGGGCGAAGACGTAGTCGTGGATGCCGCAGCCGAACTCCGGGCGCATGGGGCGCTCGCCGGGCGCGGTCGCCAGGACCAGGCGGATCGCCTCCTCGATCTCGCGCTCGCGCTCGACCAGGGCGATGCCGCCGGTCGGCCCGACCCGCATCGGGAACGCCCAGCCCCGGCCGATGAACCGGTCGCTCATCGCCCGCCCCCGATCTGGACGTTCGGCGCGCCGGCCAGCACGGTGGCGCCGCACGCGGTGGTGTCGCCCATGCGCGCGGCGGGCACCCCGCCGATGAGTACCGTGCCCGCCGCGAGCGCGGCCGGGTTCGGCAGGATCACGTTGGCCGGTCCCATGGCCGCGTGCGGGGGCATCGGGCAGGCGTGGAGACTGCCCACGACGGCGGCGGGACGCCCGCCGATCAGCACCCGGGCCACCACCGCCGCAGCGACGGGCGGCGGGGTGCTGATCAGGCCGCCGTGGCTGGTGGGGTCGCCGGTACGGGCTGCGGCTGGCATGCGGCACTCCTTGCGGAAGGTCTCCGGCCCGCGGGCCGGGGGGCGGTCGTGGTCTGCGGGGCGGGCGGGCGCGGGCGCCGTGGTGCCCGCCCGCCGGGCGGCGAAGGGCCCGGCGGTGACGGGCTGCTGGTGCGCGAGGGACACGGGCGGCCTCAGTTGATCTTGATGAGACGGGCCTTGAGGACGCCCAGCAGACCGCCGTCGACGGTGGCCTCCGTCTGCCCGGTGACCCGCACCGAACGGCCGCCGACCGTCACCGTGTCGGTGGCGTCGATCTCCACCCGGCGGCCGCGTACGGTCACGTCACCGCGCCCGGCGTCCAGCGTGATGCCGTCCCTGTCGAGCAGGACGGAGGTGAGGGGACGGCCCCGTCCGGCGTACACCGTGAGCTCGATCCGGTCGCGCCGGTCGTCCAGGCGTACTTCGAGACGCTCGTCGCCCGTCGTGAGCCGCAGCCCGGAGGGGCCGGGCGCCCTCGCGTCGAGGAGTTCCACCCGGTGCCCGGAACGGGACACCACCGAACGGCGGTTGACCCGGCCGCTGGTGGCGTCGACCAGCGGGACGTCGTGGGGCGACGGCCGGTCCACGCCGTTGTAGAGCCCCCCGATGACGTACGGGCTGTCCAGCAGGCCCTGTTCGAAACCGACCAGGACCTCGTCGTTCACCTCCGGGCTCACCACCCCCCCGCCGCCCTTGCCGCCCCACTGCACGGTGCGGACCCAGTCGGTCGTGTAGGTGTCGTCCAGCCAGGGGAACCGCAGGCGCACCTCGCCGCGTTCCGCGCCGCCGGGCTCGCGCACGTCGGTCACCACGCCGATCGCCAGGCCCGGCATGCGCGGGCCGCGGCCCGGCGCGTTGGCCCCGGTCACCAGGCCGGTCAGGGAGCGGTCGGGGCTGGCGCTCACCCACACCGTCGTGCGGTAGCCGCCGTACGGCTCCAGGACGTGCCGCACCGCCGTGGCCGTGTAGCGGCCGGAGAACGCCGGCCCCACGTTGCCGAGCGCCACGGGCTTGCCCGCCCGCAGCCGGGGGTTGCCCTCGGCCACCGCCTCCAGCTCCCCGAAGCCCGCGCTGACCTGGGCGGCCATCGCGCCGGCGGCCGCCGTCGTCTCCGCCTGCGTGCGGTACGGGGTGTCCGTGACGGCCAGCTTCGCCGACGCGCCGAACCGGGCGCCGGTCTGCGGGCTCAGGCCCGGCACCACCGTGTCGCTGACCACCGACGGCTGCCGGGCCACCAGCGGCTTCTTCGTGGTGACGTCCCAGCCGCGGACCTCCACCGACGCGGCCCCGTCCGCGGCCGACAGCGCGGCGCGCAGCGCCAGCAGGTTGCGCCCGTACTCCAGCACCATCGGGTCGCGGGTCGCGGAGGTCGAGGGCGCGGGCGCTCCGGCGGCCTTCTCGGGCCGGGTGAACTGGAGCACCCCCTGGTCGTCGACGCGTACCTGCGCACCGCTCTCGCCCGCCAGGTACTGCAGGAACTCCCAGTCGGACACGTTCGCCTGCGAGAGCTGGCGGTAGCTGACCGGCGCCGCCTCGACGGTGCCGCAGGCCAGCCCGGCCCCGGCGGCCACCTTGCGGACGATCGCGGCGGCCGTCATGTTCCGGTACGCCACCACCTTGCGGCCCCGTTGCAGGCGGTGCGCCTTGGAGTAGGCCCGCACCACCGTGAAGGAGCCGGTGCTGTCCCGGTCCACCTCCAGCGCCGTCACCTCGCCGTTGAACAGCCGCTCCCGGGCCCGCCCCGACACCGTCACCACCGACACCCGCAGCGGGGTGCCGATGGTGATGCCGGTGGCCCGCAGGAACTCGTGGTCGGGATCGCGGAAGGTGAGCACCGCCGCGTCGGGCAGGCCCACGTTCTCGTCGACCACGCAGCTCACCAGTTGCGCCGCCCAGATCTTCGGCAGTTCGGCGGGGGCCTCCACTACCGGGTCGGCCGCGAACGACCGGCCGCCCTGTGCCTCGGCTGTGCTCACCGCTCCTCCTCAGCACCCGCGTCCCTGAGCCCGGGCACCACCAGTTCGGTGCCGGGCGCGAGGGCCATCGGGTCGTCGATGTCGTTCGCCTCCGCGATGACCCGCCAGGCCGTGGCGTCGCCGTACTCGCGCCAGGCCAGCAGGGCGAGGCTGTCGCCGGCCACCACGGTGTGGGTGCTGCGGGCGGTGCGCGCGCCGGAGGTCGGGTTCTGTCCCGGTGTGTCGACGCTCGCCTCCTCGATGGTCAGCGCGCAGGTGGCCCGCAGCGGCCTGCCGTCCACGTCGAACAGCGTGTAGGTGACCGACAGGCTCGACAGCACGCCGTCGAACGACGTCGTCCGCGCGGTGCCCCATTCGAACCGCACCCACGGGCTGGCGGGCTTCTTGCGGCCCAGGCTGGCCGGGGTGGGCACACATGCCTTCATCAGCTTCTCCACCGCCTGTTCCACGGAGTTGTCGTGGGTGGCGGTGGCGTCCAGGAACACCTCCAGGCTCAGCGTGCGCGGGCCGCTGCCGACGAACTCGGGCAGCGCGGACTCCTCCGCCATCCGGGACGGGGAGCGCCGCCACTCGGTGGTCTTGCGCAGTTCCAGGGTGGAGGGGTTGAACTGGAGGTCGAGCCGGGCGATCGTGCCGCCGGGCTTGGCGCCGACCGAGGCCGGGGGCTCCTTCAGGGTCAGTTGGGCCCTGGCCCGGCTGGAGCGGACCGCTGGGGACATCCCGGAGCCTCCTTTCTGGGCCGGTGCCCGGGGGCGGGGTCGAGGGGAACGGCCGGCGGGAGCCGGTGGACGTCGGCGGACGTCGCGTGGCGGCGGCCGGGGAAGTGGGCGGCGCGGCCGGTCACAGCGGCCTCAGGCCCTCGTGGGCGATCTCCAGGGTCTCCACCGCGGCCTGGGAACTGGCGGGGTCGAAGGACGGCCCCTGCCAGCGCACCGGGACGATCCCGAACACCTGCCAGCTGATGATCCGGCTCAGGTCGGGTTTCAGGGCCACGATCTCGCCGTCCTTGGGTTCCACCCGCCGCAGCGTCTCGTCGAGCCAGCGGCCGATCTTCGCCGTGTCGGCGGTGACCGGCCGGGTGAGCGTGATGTTGGACCACGTCACCCGGCCCGGCAGGTTCCAGGTGAAGCCGTTGTTGCCGCCCTCGGCGTAGGTCTCCATCTCGACCTCGGCGCCCATGCCGGAGCAGGTGTGGAAGGCGCCCAGGTCGTTGCCGCCGATCGCGAGCCGGAAGAACACGCTCGTCGCGAAGATGCTGTCGGTCATCGGTCCGTCATCCGTTCCGTGCTTTTCCGTGCTTTCCGTGCTGCTTGGGACTTCCGGGCTGTCCGTGCCGTCCGTGCCGTTCGGGGCTTGCGTGCTGTTCGGGGCTTGCGTGCTGTTCGGGGCTTGCGTGCGTGCCGTGCTTTTCCTGCCGTCAGCGGCGGCGGTCGTGGGGGCGGCCCATGCGTTCCCGGCCGCGCCGCAGTTCGGCGCGCAGCAGCCGGGACACCGGGTCGAGCAGGCGGCGCGCCAGGTCGTCCAGGTCGTCCCGGTCCGGACCCGGGTCCGGCGGCGCCCCCGCCCGGTGCGCGGTGCCGGAGGCCGACGTACGGGAGACCGGCGTACCGGAGGCGGACGGCGGGGAGGCGGATCGCGGCCCGGCGGGCGGCGCTCCCCCGGCGGCCTGCGCGGTACCGGCGGCCTTGCGCTGCACCACGGGCGCGACCGGGCCCTTCTCGCCGCCCGTCGCCGGTCCGGGCCCCGCGGGAACGGCACGCGGACGGACCACCGGGACGGAAGCCGGCGGGGCCGGTGGCACCGCGGCGGCGGCCGGGCCCGTGGGCGCGGGCGTCCGGGCCCCGGCCACCGGAAGCGACCGTGCCGGTGCGGCGGCGGGCTGGACGGTGGTCCCGGGGGTGCCTCCCCGGTGCGGTGCGGGACGCACGACCGGGACGCCCCGGCCGGAACCGGCGCTCGCGGCCCGGCCGGTGCCCGCTGCGGCCGGCCCGGGGCGCACGGCCGCGGACCGCACGCCCGGGGGCGCCGACGGTGTGGCCGCGCCCGGCGCCGGGCCCGGGTGCGGGGTGGTCCCGCTTCGGGGGGCGGCGCTCACCCCCGCCGGTGCGCCGGTCCAGCGCGCGGCCACCACGGGACGGCCTCCGGGGCGGGAGGCGACGGGCGGAGCCGCACCTTCCGGGAGCCGGGTCTCCGTACGCAGCGGGCGTGCGGCGAGCAGGGGCAGGGTGCGCGGTGCCGCCGGGACCGGGAGCACCGGGGCGCGGCTCACGGTGAGCGCGCCCCGGCCGGCCGCGTCCGGGGACGGGGCGGCCCCGGCGCCGGTCCGTACGCCGGCACCGCTCGCACCACCGTGCACGGGCCGGGCCGCGGAGACCGGGCGGACCGGGACGACGGGTTCCCGGGGCGGTTGCCCGCCCGGCCCGCGCACGGTGGCCGGGCGGGCACCGCGGGGGTCGGCCGCCGCCGCGACGGCGCCGGTGGCCTCGCGGGACGCGGGGCGGGCCGCGCCGTCCGACGAGGGCTTCACCAGCGGCCTGGCGGAATCCTGGCCGGGGTCGGCGGAACCGGGTCGGGCGGCGCCCTCGGCGGCAGGGCCCGCGAGGCGCTGGACCTCCCGCGTCCCCAGCAGCGGGGAGTGCTCCGCGCCTCCCGGCGGCGAACCCGCCGACGACGGCGGCGGGGCCGCACCGGGGGCGGTACGCGGCGCCGCCGTCCGGCCGCCGTCCGTACGGGACGCCGCCGACGCGGTGTCCGCGCCGCCGTCCGGGCGCGCCGGGGCACGCTGGACGTCCGGGCCGTACCCGGTAGGCGGAGCGGGACGGCCCGACGCGGCGGAACGCGGCAGTTCGGCGCTGGGCGGCAGCGCGGACAGCGGCGCGCCGAGGCCGCCGCGGGCACGGGCCCCGCCGCGGCCGGTGCCGGACGCCGGGTCTGTGGCACCGGCCCGCGCCGCCGGACCGCCGTGGGCCGTCCGCCCCTCCCCCACGTCGTGCGGTCCCGGCGTCCCCGCACCGTCCTGGGCGTGGCGCTGGACGACGGGCAGCGCCGGGCCGGACGCGGCGGGGGCGCCGGCCGCCGACCGGGCGGCGGGGGCGGACGGGCGGGTGGAGCCGTCCGCCGTGGGCAGGTCCGTGGCGGGCAGGGCTGTGGCGGGCAGGGCGTTCAGTGGCGCGCCGAGGGGCGCGCGGTCTTCCGCGCTCCGGGCGGTGCGCTGCGCCGGACCGGTGGCCGGTGCGACGGCTCCGGCGGGTGACGGTGCGGCGGTGCCGCCGTCGGCGCGGTCACCGGGCGCCGGGAGTACGGCGGGCGGCACAGCGCGGACCCGGCGCACGGGTCCGGCGGGGCGCCGGGCGACGGTCAGCGCGCCCCCCACCGGGCGGACACGGGCGGCCGGGAAGGAGGCCCCGGCCTCGACCCCGACCCCGACCCCGGCCCCGGCCCCGGCCCCGGCTCCGGCTCCGGCTCCGGCTCCGGCTCCGGCTCCGGCGGCGGATGCTTCCTCGGAAGCAGCCGAGGCGTCAGAGGTACCAGAGGCGCGAGAGGGGCGGGAGACATCGGAGCCCCGGGAGGCGGGGGCGTCAGAGGTCCGGGACGCGCCCGCCCGCTCCGGCCCGCCGCTCCGGGCGGCCCGGCCGGGCGGTGTGCCTCCGGAGCCGGACGGCGTCCGGGGGGTGTGCTTCGGCTCCGCCCCGGACCCGGTGGAACGCGTGCGCGGCGCGGCCTGTGTCTGCGGCCGTGCCTGTGGCCGTGTCCGTTCCTGGGCCTGTGGCTGTGTCTGTGTCTGTGGCTGTGGGGCGTACGGCCCGCCGGAGGCACGCCGGGCGGCACGCTGGACCACCGGCTCGTCCCGGCCCGGGCCGGGGGTGACCGCCGCCACCCGCCGGACCAGCGGAATGTCGGCGATCGGGCTCGGTCCGCCGCCAGGCCGCTCCGCCCGCTGGACGGCGGGGGGCGCCGAGGGCAGCGTTCCGGCGGAGCCGGCGGACAGCAGGCCCCGGGACCGCGGCGCGCCGCCCGGGCCGCCGGTGGGCGCACCGGCCGGACCGGACGTACCGGCCGGGTCGGATGAACCGGGCGAACCGGCCGGGTCGGAGGGAGCGGGCCGGGAGGACGGACGGGACCGGGGCGCCGGGCCGGACGAGCCGGACGCCCGCCCTTCCTGACGCGCCCCGCGCGGGGTCGCGGGCGGCGGGTTCTGCCGGTCCCCGCCGTCCGCGGCCTGCCCGGTCTCGGCGGCGGGCCGTGGTTCCCCCGCGCCGTGCCCGCGCGGCGCGCCGAGCAGCAGCGGGCCTCCGCCCGTGCCGATGGTGCGGGGGGTGGCCGGACCGACGACGCCCCGCACCACGCCCGCCGGGGCCGTGGGCAGCACGGCATGCCCCAGGCCGGTGCCGAAGGAGGGGTTCTGCCAAGCGGTCAGGCCGGCCCGGAAGGACAGACCGTCGCTGACTCCCAACGGCGCGCGCGACAGGGTGAGTTCCGGCGCCGCGGTGCGCCGCCATCCGCCGTCCCAGTCGCCGGGAACCGAGGAAGCAGGCGCCGCGGCACCGGGTGCCGCGGTACTCGCCCCGGAGGCGTCGGACCCGGAGGAATCCGGCCCGGACGGCGACGCGGGACCGGGCAGGGCGGAGCCCCGGGCGTCAGGGGCTCCCCCGTCCCGGCCTCCGGCCCCGGAGCCGGACGGACCGTCCGCTCCGGCGGCCCGGCGGCGCAGCCTGTCCCGCCATGCCATGTGCTAACCGCTCTCGTTGATACGGGTGTTGATGCGGGCGATCTCCGCCACCCACTGTTGGCGTTCGCCGTGGGTGAGATCGAGGATCTCCTCGCGCTGCCAGTGGAAGTGGTAGGCGATGTACGCGATCTCCTCCCGGAGCCGGGGAAGGGCGTACGTCACGATTCCCCCAGGCGCCCACCCGACAGGTCGACCTCGAAGCCGCCCTCGCAGTGGGGGCAGGTCACCGCCGCGCGGGTGTGCCCCTCGCTGTTGACGCGACGGTAGAAGTCCTGGAGGAAGGCCACGTCGGTGGCGTACATCCGCTCCACGATCCCGGCGTGCACGTCGGTGATGGTGCCGATCCGGGTGATCACCTGGCTCAGCAGCACCACGCTCAGGTACGCCGGGTTCTCCTTGACCCTGAGGTCGATCTGGGGCCGCAGTTCGTCGCGGGCGGTGGCCAGGCGCATCGCGCCGTCGCGGTGCAGCACGCCCGCCTCGTCGACGTACCCGCGCGGCAGCTCGAACTCGAACTCGGTGCGCAGGCCGTGCTCCTCCCGGGGTGGCGGCGGGGCCGCGGGGGCCACCGCCTCCTGCTCCGTCTGCGGGGCGGGCGTCGTCAACTGGAGGATCTCCTCCAGATTGCCCGCCGTCACCGTACGGCGCCTCATTCGACGACGATCTCCTCGAACACGATGGTGACGGTCTCGGTGGCCGCGGAGGACTCGCCCGCCTTCAGCGAGGGGCCCTCCCACTTGGAGGCCCAGCCCTGCATGAGCTGGATGCGGCGGACCGTGGTGCCCTCGGAGTCCTTGATCTCGATGGTGAGGTTCTGCCGCGCGGAGTTCACGGCCCCCTTGTTGAGGGTCTCCTTGATCCAGTTGGTGAACTCGCTGCTCTGGTCGAGTCCCCGGGTGATCGTGATCTCACCGGCCTGCCGGGCGCCGGGCTGCTTGCGGATGATCTGCTTGCCCGTCGCGCTGACCTGGCGGACCTCGACGACCTCCTCCTCGACGGTCAGCCCGCTGATCTCCTGGATCGACTCGACCAGGTAGCCGCCGAGCTGCACGCCGAAGACGTGGGTGGAAAGAGCGTCGCCCTCTGCCATGACTGTCTGTCACCTTTCCTTGCGGACCCGCGGGTCACTCGTCGATGAGGCTGGTGCTGTCGGAGAACTGGGCCAGCCGGAACACCACGAACTCCGCGGGCTTGACGGGCGCGACGCCGATCTCGCAGACGACCCGGCCCTGGTCGATGGACTCCTGCGGGTTGTTGTCACGGTCGCACTTGACGTAGAACGCCTCCTCGGCCGTGCGGCCGAACAGCGCTCCCCGGCGCCACTCCTCGGTGAGGAACGCCGCGACATTGCGCCGGATGCTCGACCAGAGCCGGTCGTCGTTCGGCTCGAACACCACCCACTGGGTGCCCAGGAGGATCGACTCCTCCAGGTAGTTGAACAGGCGGCGCACGTTCAGGTAGCGCCAGGCCGGGTCGGAGGACAGGGTGCGGGCCCCCCACACGCGGACACCGCGGCCGGGGAAGGCCCGTACGCAGTTCACGCCGATGGGGTTGAGCAGGTCCTGCTCGCCCTTGCTGAGCCGGATCTCCAGGTCCACGGCGCCGCGGATCACCTCGTTGGCGGGCGCCTTGTGCACACCGCGCTCGGCGTCGCTGCGCGCCCACACGCCGGCGATGTGGCCGCTCGGCGGGACGGTGGTGTTGCGCCCGGCGGCCGGGTCGAAGACCCGCACCCAGGGGTAGTAGAGGGTGGCGTACCGGGAGTCGTAGCCCGCCTCGTCGTTGCGCCAGGTGCGCGCCTGCTGGGCGGTGAGGCCGGGCGGGGTGTCCAGGACGGCCACCCGGTCGCCCATCTGCTCGCAGTGCGAGATCACGGCGAGCTGTACGGTGCGCACGCCCTCGGCGTCGATGTCCCCGCGCTGGTAGGCGCTCATCAGGTCCGGCACCGCGACCATGGTGATCTCGTCGATGGTCTCCAGGCCCCCGAACCCGGTGCGGGCCGCGGCGTCGCCGACGTACTCCGACGGGTCCAGGCGGGCCACCGCACCGGGTGCGGCCGGGGCGTCGGGCAGCGCCACCGTCTGGGCGGCGGGCCTGGCCTGGGGGGCGTCGCGCCGCTCGGTGACCTCGACCAGCTTGGAATTGCGGGCCTGGCTGACCAGATACCCCTTGACGCTCTTGCGGGTGGAGGCGTCGAAGGTCTCCACCACCTCGCCGCCCTGGCGCACCAGGAACCGGAACCGGTCCTCCGGCGGGTCCTCGCCGGGTACGTCGGCGATCTCCACCGACACCCCGACGGCACCGGGCCGGGCGGCGACCAGGAACCCGCCGAGCTCCACCGGCCGCGGCGCACCGGCCTGCTGTCCCCGGCCGGTCCCGTCGGCGGCCGGTGCCGAGGCGTCCTCGGCGGAGCCTCCGATCCGCACCACGTAGGCGGCGCCGCCGCCGTTGGCGAAGTACCCGTAGACCGCGTGGGCCAGGTAGGTGCCCTCGGTGAAGCCACCGAAGAGCTGGGTGTACTGGTCCCAGCTCGTGACCAGGGTCGGCGTGTGGAACGGGCCGGCCTCGGCGAACCCGACGAACGCGGCGACCGCGGTACCCACGCCTTCGATCGGCCGGGCACCGGACTGCACCTCCTCCACATACACACCCGGGGTGAGGTACGTCGGCAT

Protein sequences of DBSCAN-SWA_2

>NZ_LN831790|2005371:2058129|2043292_2043922_+|WP_048574340.1|DBSCAN-SWA
MTAGYRRRIAERVARLGATPGFSVRAYEVAPPVTDAELASVTASAQGRLPVGVAEFYGELNGFRLEWEYTAPEGGGPPTDFGSVNVRPLADVFAEGLGDTWYDDFEGGDRFRAVKPFDVYAPEACAAFLQEPGGAPRDDVHFHYFGESLSPLHLTFPQYLEGALASCGYVDWRMALTPDDPGLPAARRTLERMRAIIPGFDGLPRPGSA
>NZ_LN831790|2005371:2058129|2056106_2056547_-|WP_029386828.1|tail|DBSCAN-SWA
MAEGDALSTHVFGVQLGGYLVESIQEISGLTVEEEVVEVRQVSATGKQIIRKQPGARQAGEITITRGLDQSSEFTNWIKETLNKGAVNSARQNLTIEIKDSEGTTVRRIQLMQGWASKWEGPSLKAGESSAATETVTIVFEEIVVE
>NZ_LN831790|2005371:2058129|2045494_2046058_-|WP_029386816.1|tail|DBSCAN-SWA
MSRAAVPGLPSRYPIGGQLPALYAEDDLAQRFTAGLDTVLAPVFSTLDNLPAYLDPRLAPADFLAWLASWVGATDDRAWPMEVRREAVVRAVELHRWRGTRRGLVEALGLALGAHAEVTGDGGALWSGTPGAELPPAPAAEVLVRVWPGREERIDPDRVREIVRAMCPVHTVCRVEILPGPPAGEGR
>NZ_LN831790|2005371:2058129|2048431_2048752_-|WP_029386813.1|DBSCAN-SWA
MPAAARTGDPTSHGGLISTPPPVAAAVVARVLIGGRPAAVVGSLHACPMPPHAAMGPANVILPNPAALAAGTVLIGGVPAARMGDTTACGATVLAGAPNVQIGGGR
>NZ_LN831790|2005371:2058129|2038282_2039734_-|WP_029385190.1|DBSCAN-SWA
MDGPQPTTRSGAVVATLALAGTVAAIMQTLVTPLIAEMPQILDTTPSNAAWVVTVTLLVAGVCVPVSGRLGDLLGKRRMLLVCAVPLVVGSVVCALASSVVPMIIGRGLQGMGMGMVPLGIALLRDVVPQERLSGSIALVSASMGIGGAIGLPLAAAVAQYADWRVLFWGAAVLALSVGTLIFFFVPDVPAGAKGQRFDAPGAVGLAIGLVSLLLAISKGGDWGWTSGTVLGLFALAVVSLAVWGLYELRTREPLVDLRTTARPRVLFTNASSILIGVGMYAFMLIAPQLLQFPEATGYGLGQSMLAAGLYLAPGGVMMMIVSPLGGKLINARGPKFTLICGALVIAVGYGIALPLMGTAWGLMLVGIVINSGVGLAYGAMPALIMSAVPVSETAAANGFNTLMRSLGTTIGSAVIGVVLAQMTITMGGHTLASEDGFRTGLLIGCGVAVAAAAVALLIPAGRTGTGDSAAAKTPAGQEPART
>NZ_LN831790|2005371:2058129|2043999_2045490_-|WP_166520570.1|DBSCAN-SWA
MRACPACGASNDPQDDFCGNCGAYLGWSESAAAAPGRAAEPPADPAADSDPAPVTGPVPRGAAAAGSVPTPAAVPAPDAAPAPSPPPEAAESARRTGESAAAPGASARPPARRGSAPAGPDSAGDTAPGTDAETQPESERAAGPERETEPERAAGPEPEAPASARRETGRARRRTPPALGRPGRGERPAPGPARSSAPPPGQPPAPVAPVTPAAPGDARSDPAPRPPSAPAADASAPGPVLPVRPGRPVAPRPTVRPVAVPDDVAGTPCPACGTPNPPGRRFCRRCAAVLNPEEKPPPLPWWRTVWPFRRRARASSGRVARLLVILAVVAALCAGGFLLLPAGRALIEDTRDKLGKPKPITPVSVEASDEVPGHPARNTTDGLSNRYWGASAEGASVTYTFRRPFRLVDLLITNGASASAQPYARQARALELELEVTTQDGTRHTKKLTLGDKPGPQPVPTGISDVKTVRLVLRSPTGLAPGRHLALAEVEFFQRS
>NZ_LN831790|2005371:2058129|2005371_2006082_+|WP_029387628.1|tRNA|DBSCAN-SWA
MSQDQDPTPVNAPPARPAAGAPEYVLPLVVRIERAAPPPRTDALQTSARAVLVMLADERSVGDGEWAQAMRDWQDARIRKVVRRARGAEWRRAEALPGITVTGKAAEVRVFPPVPLDGWPKDLARLQVSGTDLDDPEAPVDADPSAPVLWLNPDLEMSAGKAMAQTGHGAQLAWWALPDEERAAWRDAGFPLAVRTADPADWRRLTTSGLPTVRDAGFTEVAPGSCTVVADHPALR
>NZ_LN831790|2005371:2058129|2006119_2006941_-|WP_029387627.1|DBSCAN-SWA
MSDHPGPPTVSPALFGMGSGDWLPVTAGESGAFVFRSADAARYAKCVPAAEAAGLEAERDRVEWLNGRGVPGPRVLDWYSGEAGVCLVTSAVSGVPADQVSAEELRLSWGRIADAVRRLHEVPVAECPFGRELDAMLALARDVVARGAVNPEFLPVEQQHLPPAELLARLTGQVPRRREQEAADTVVCHGDLCLPNIILDPRTLDVSGFIDLGRLGRADRHADLALLLANARETWPDEEWARAADAAFAERYGIAVDPDRLRFYLHLDPLTWG
>NZ_LN831790|2005371:2058129|2030913_2031975_-|WP_029385196.1|DBSCAN-SWA
MTRSAIPDEYLEGYAEILAGVCATGRRLTRNELESLRTRGERAAEAGLGLRLLVRRHLAAARELSPALSPAGADRVLAAVEQAVDAFAEGYERSQKLAVRQEEAARREFIDDLLYGRSDLGRLAERAERFGLLFSRAHAVAVAQGATPVDDTHPATRQVESALVARFGERRILLTTKDGRLVCIAPGDQGDVLAFFAKQAHAATDGGRVALGRAHPGAGGVVHSYEEALNALDLADRLELEEPVLRSADLLVYPVLTRDRQAMADLVRSALGPLQAARGGAQPLLDTLTAYFDSGCVAAEAARRLRLSVRALTYRLERIHQLTGTNPADPVHRYTLQTAVIGARLLGWPGNEI
>NZ_LN831790|2005371:2058129|2046054_2048013_-|WP_029386815.1|plate|DBSCAN-SWA
MALPSPNLDDRRFQELVDEAKRYVQQRAPEWTDHNVSDPGVTLIETFAYLVDQLLYRLNRVPDKNYTAFLDLLGIRLFPPAAASADVDFWLSAPQPDTVVLPAGTEVTTTRGETDDAVVFTTTDELHIAPSELTRLVTAPRAGEQTDRTRTLAEGRDIPCFQAAPEPGDALLFGLPTAVPRCIVAVRLDSRVEGVGVDPRQPPLVWEAWHGSGWQVCETGPDTTGGLNRPGEVIVYVPAGHRASVIGGTRAGWLRCRVTEPEPGQPFYSESPTVREASVFTVGGTMCAEHAVTVTDVPLGTSEGVAGQTFRVGRPPVLLDGAPPVVEVSSAEGWQRWDVVEHFGRSGPADRHVRVDATTGEFAFPPALREPDGTLRQCGAVPPKGAQVRVARYRTGGGPAGNVARGAISVLRSSVPYVARVTNREAARGGVAGETVANAKLRAPEALRMQERAVTAEDYEILSRQAAPSVRRVRCLPAADGPGAVRVLVVPDAVPDEGDRLRFEQLIPSDRVLQAITSCLDERRLIGTRLVVEPPVYQGVTVVARLTTAPGDADRVREAALAALFGYLDPLRGGPEGTGWPFGRPVQYGEVFGVVQRATGDALVEEIRLFPADPITGRRGAPSDRIDVGAGALVFSYQHQVVVTAAGPEDRG
>NZ_LN831790|2005371:2058129|2032186_2033716_-|WP_029385195.1|DBSCAN-SWA
MSSVVIAMGGVVVLLVLIALVVVSRYKVAGPSEAFIVTGRRGKKATDPETGRVFTDNSGQKVVVGGGVFVVPFVQQKFALDLSSRHIPVAVRGAVTLRGVKANLEGVAIVKVGGTEDAIRAAAQRFLMQQDGIVGFTQEVLSGALRAIVGRMAVEDIIRDRAAFAGQVAEEAEASLSGQGLVLDAFQIQDITTEGSYLEDLGRPEAARAKQEADIAEAEARRAAEQARLKAEEEIAVAQRTLYLRQAEIKAETDQAAARANAAGPLAEAARQQEILTEQEKVAERQAALTDRQLDTQVRKPADAQRYAAEQEAEAKRVARVKQAEAERLAEIAAAQAEAERSRLTGEGEKQRRSALAEAQAIEGLKQGEAERARRAAIAEAVRLEGEAEAAAIGARGAAEAEAMEKKADAFARYGDAAVLQMLVEVLPQVVAKASEPLSAVDKMTVISTDGASRLSRTVADNVAQGMELLGSTTGVDLAELLKGITRRNGDVQPADPSAAEADGKIQIG
>NZ_LN831790|2005371:2058129|2033821_2034337_-|WP_029385194.1|DBSCAN-SWA
MAWFLGLGIAGVVLLVLSFVLEGVLEGLLDGISVVDGLLDGLLSLPVIAGFLSVLGFSGAIVLGTTGLGAVGATVIGVPAGVLTGWFAYRLSRALMRDYSGAAPRDDDLIGVSGSVVTAIPADGYGEVLVRLAGQPVKLAAKSPVAVARGAEVWVEQTLSQSAVSVRPVER
>NZ_LN831790|2005371:2058129|2015101_2015401_+|WP_029385269.1|DBSCAN-SWA
MADQQTGSGFSIKMCDLPVTLPAREDSEWSLREILEWAPEHSDWGAKRICVAGCGVTCLEVPEGTLIEVPTEDALDMRLVAPAEVERRLAENRLWRDPE
>NZ_LN831790|2005371:2058129|2039845_2040364_+|WP_078648312.1|DBSCAN-SWA
MGELQGVAPQRRGHVNTADRSTAQVEFEQMLLSRYMHLHKSKGRRADSALDRSAYILLSRIRAQGPMSIGQLGDAFGLDASTLNRQTAAAMRAGLVERIPDPEGGMARKFRITDEGERRLDEERAGLVASLDRIMADWPEEDIAAFAGYLRRFNSDIERLHGMPWPRACVNP
>NZ_LN831790|2005371:2058129|2025091_2026024_+|WP_029385202.1|DBSCAN-SWA
MRARRSVRPGRPLAGLLLAAALALTGCSAGGEDSAGSGSAADAAKEAASQADGRGGGAYRGDAGGAKASAPQKLTTGHIIRTASLTVQVDSVPKALDAARADAESAGGYVGNETTTRDEDGRERTRVVLRVPVERYDGVLAGLEGAGKLLERSAKAEDVTDQVVDVESRIKSQRASVARVRALMDQATKLSDVVTLEGELSSRQAELEALLARQASLKDRTTLATITLSLTETPVRESEREDDPGFLDALAGGWDAFVTMLRWLAVALGAVLPFAAVAALLVLLWLRVVRPRRPGGSAGPDISAGTGGQG
>NZ_LN831790|2005371:2058129|2037253_2037631_+|WP_029385192.1|DBSCAN-SWA
MTSTQNYGTCVDVQVDPDGPPVTSASSFVTFTAPLSCLLSPPVLEVELIIHWNGGRTSTAQALAVVSRTTGTTIATDTGTITSGLFAGKTINVTVVYPTLDVTGCLLGDGVSEISGAATLVVAPV
>NZ_LN831790|2005371:2058129|2055615_2056110_-|WP_029386827.1|DBSCAN-SWA
MRRRTVTAGNLEEILQLTTPAPQTEQEAVAPAAPPPPREEHGLRTEFEFELPRGYVDEAGVLHRDGAMRLATARDELRPQIDLRVKENPAYLSVVLLSQVITRIGTITDVHAGIVERMYATDVAFLQDFYRRVNSEGHTRAAVTCPHCEGGFEVDLSGGRLGES
>NZ_LN831790|2005371:2058129|2018689_2020087_+|WP_029385265.1|DBSCAN-SWA
MERLGTGIGWRPEIADAVERMPGIDWVEVVAENVCPGHLPASLRRLRERGVTVVPHGVSLGLGGAERPDPDQLTALAERARALDAPLVTEHIAFVRAGGPLTATPRLEAGHLLPVPRTRDALDVLCENVRVAQDALPVPLAVENIAALFSWPGEEMTEGQFLYELADRTGVRLLIDVANLHTNHVNRGEDPAKALAELPLEAIAYVHVAGGFERDGVWHDSHAHPVPPPVLGILAELAARVSPPGVLLERDENFPAPAELEGELEAIRAALRAGRRLATGEHAGETGRVPAGAAHPAHPAHPSRPEGPDGPVPPAGAGEGPVDSPGTGPARERLGLAQAALLSALVAGTPAPEGFDRVRLRVQTRALAAKRAGVVAKVAPELPEILGDGYRPAFLAYAHGRPMTGGYRQDALDFAERLLGDGLPVDARARRALRQWWLERSGPVPRSRRPAVRLARATRRVLLRR
>NZ_LN831790|2005371:2058129|2007445_2014306_+|WP_079164117.1|DBSCAN-SWA
MVMFVGLIPDDASAASGSSRVPDVKREPSVPGRDFTKKRPGIRNDAAVDWRPTAGTVSSQSFTTQVTGGGGERAGRAPLLSGSGGGEAAGVRTSPVRIRKAGTIGKRDGVRITGRAAKRAPAAPGSAVRVQVKDMATARKAGVQGLLLTAEPATGATAPAASGSVDVELDYSSFKDTYGGDWASRLRLVRMPACALTTPGKAGCRTVTELPGVNDPVARTVSATVDLAPAGAPTVLAATAAASGPGGSHEATSLSPSGSWMAGSSSGGFAWTYPIEAPEVPGGPQPEVELSYSSQAVDGRTASTNAQSSWIAEGWDYEPGYIERRFRSCSDDKGEVGGVKPNNTGDSGDLCWGSDHVVMSLGGSTTELVKKDGTDEWRPADDDGSRLQRKTGAANGGHGGEHWVLTTTDGTQYHFGLNKLPGAPEGTVTNSALTVPVFGNHPGEPCHATAFTDSDCAQVYRWNLDYVVDPLGDAMTLWWTKETNHYGQNMKADQPASYVRAAQLARIDYGLRSDKLFGVLPAGRVSFTTAERCIPSTAFDCAESKRTAANAKYWPDVPLDQECAAGAKCTDKYSPTFWTTKRLTKITTQVLSGTALNTVDSWTLEQSYPATGDGTSPALWLDSITRTGHRAGATAAMPKVTFSGTQMDNRVDGVEGLPPFSRQRIHAIDTETGGRIAVSYSARECQALEPRKMPASPESNTLRCYPQYWTPKGALAPVKDWFHKYVVTQVSEQDLVTDSPSKVTSYEYLGSPAWAWDDSEFTENKHRTWSQYRGYERVRTRIGGGTDVRQLTEHRYFRGLHGDKLPSGTRTSTVTTSDGSSFQDLPQYQGQLLEQITYESDGGPIDSATVTTPWSVKTATRTRSGTTPLEAWMTRPEKVLTRERVKGETWRTSTETTAYDSYGLPYQVEEKSPGGTVRCSTVTYARNTSVYLIELEAREKTVLGACGTTGGEVVEDTRTLYDNLAFGAAPVKGLPTEIQELDGTGEGYLTIDRTEYDIHGREIATWDADNRKTSVVYTPATVQRPVRQVSTDPLGHTETTDFDTLRGLPLVETDANGKKATMEYDPLGRLLKVWETDRDPATQTPTATYDYTVRRDGPTIVTTRTLKDNGEYAVSYEILDGLLRERQTQDEAIGAGRIVNDTFYDSAGRVWKENDGYYNSAEPEPVLLQVGDNDVPSQNRTTFDGLGQPTAEITYYRGTEKLRTTTERDGDVSTTIPPKGDTVTAVFEDAEGRTERLREYTDAARTRWRDTVYEYDDLDNLVKVTAPGGAVTSFEYDKRGRQTAVVDPDGGRTELRYDNSDNVVAATDPDKRTLVTTYDAGGRPTSLRENSETGPKRIEWTYDTVAKGLPTAAIRYDNGLEYREEITAYDDAYRVKSTKTVIPAEETGLAGTYEYKYSYTPTGNLDWAEVPGVGGLVTERVVFVYNSDGLPIAIGGAAPYLTNVQYSAFGEILRSDSGPAGKKVYGSYVYDEFTRRLQSATFDRSVAPLRISETKYAYDEAGNVTKITDTPGDAAPDAGKTDTQCFVYDQLRQMTSAWSAKTDDCTAGPSKETVGGPDAYWQSFEFDAAGNRTKLVEHDPTGDTTKDVTRTYIYGKEGIGGPNALAEIRSVGPQGERLNTFGYDKRGNTTQRQHGGATQTLEWDVEGELRKVTEPVEGGGTKTTSYLYGADGERLIRRGADGSRTLYLGDAELTVSADNTKKTAERFYAHPDGMTTVRATGGVRQLLISDHHGTSHTVVNMAEATMGVTRRKSLPFGEARGQQPTAWPGQRGFVGGTVDKDTGLTRLGARDYDPLTGRFVSVDPMVDYGQPATMNPYAYSNNAPATFSDPTGEFFPVLIGIAARIAIQAAIRAAARRAAIIAARKAAQAAARRAAALARKRAIEAAKRAAARARREAARKAAAARRAAAKRAAARAAAKRAAARRAAAQARARAARAAARKAAARRAAARKAAARPKPRAKPRSQPKPRPKPRQVKRAVKKVAKEVREEAKETVKEEAQGATCESNSFTPGTRVLMADGTTKPIEKVKAGDKVVATDPKTGRTSVQTASATIIGKGTKHLVKVTLSVHDGSDRDGTRTTTVTATAGHPFWVPSLREWIDAGELKPGQWLQTSSGTWVQVTAIKAWTAHKATVHNLTVTDVHTYYVLAGSRPVLVHNCNENIISNAPGFDNSAELSRVSDGDVYSGVYEPSSGTFYARLSLDEKDPARFPNAVLSNGGHGEVNFWHFKGSRETIGFNMFFEKGGISVAWFSRSVNRRNHGDPMAPSGARQAIMDAISGATGRRVWSR
>NZ_LN831790|2005371:2058129|2027593_2028403_+|WP_029385198.1|protease|DBSCAN-SWA
MVIPVHDVNPVRGTPWVTYALIVANILVFVFTPGMAGSLTGDGSLAQLCHLQAFLDRYAAVPQELIHHEMPRLVPTGEVGVGPQGAGCVIAPPGYGKSPELSVLTAMFLHGSWLHLLGNMLFLWIFGNNIEERMGHLRFLLFYGVCGYAASYGFALANSDSGDPLIGASGAIAGVLGAYLVLYPKARVWVLVPFLIFLPLRLPAWIVLGLWFVLQAFYSAGQGVSDAGTVAYVAHVVGFVAGLLLAWPLKPGTPPPPQPRGALFGRRAR
>NZ_LN831790|2005371:2058129|2051568_2051994_-|WP_029386810.1|tail|DBSCAN-SWA
MTDSIFATSVFFRLAIGGNDLGAFHTCSGMGAEVEMETYAEGGNNGFTWNLPGRVTWSNITLTRPVTADTAKIGRWLDETLRRVEPKDGEIVALKPDLSRIISWQVFGIVPVRWQGPSFDPASSQAAVETLEIAHEGLRPL
>NZ_LN831790|2005371:2058129|2021116_2022733_+|WP_047121666.1|DBSCAN-SWA
MRAAVVHSAAGALLLTALAAAPAGGAPERPGAAEGPGAAERRGTAVAAARAAAAGISFGPCPDAADLPGALRCGTVTVPLDYARPDGRQIRLTVGRMRATGKDPRGGGRAVPRQGALVYNPGGPGASGLYFPLAGLSPEWKRLAAAYDLVGYAPRGVAPSAPLSCQDPEHFFPGPGPAPQQPSASYKRQRIAQARAYARGCAERSGDALRHHHSLNNARDLDVVRAALGEKRLTFMGASYGTYFGALYAELFPRHVRRMVFDSVVDPHPGRIWYRNNLAQSEAFERRWADFRAWIAAHDGVYGLGRTPGAVQRGYEVASARLSARPAGGTVGPAQLQEMLLRAVYYDDQWPHRAHALSAYLKGDPRPLIDLAEPHPEAAAEAENASAVYTAVECNDAPWPTDFRVWDRDNTRLARRAPFETWENVWTNLPCAYWPAPRQRPLEVRTGPGELPPTLLLAGERDGATPYEGALELHRRLAGSVLVTERGTGTHGVAAGPNACVNGHLEAYLLEGRLPARDAFCAPRPAPEPTSPAKSSAP
>NZ_LN831790|2005371:2058129|2034744_2036649_+|WP_099053772.1|DBSCAN-SWA
MIVCGDDALAERLAAELATVYREQVTLVVPPSRRPDATTGRARAAALLGWIQTAMNRTEGPNGSSLTGRVRLLEAAVLDEAALSGMGAREAAALALVHDDDETNIHAALAARRLNPRLRLVIRLYNRKLGQHLEELLDQAAALAVPGLDPEALDTSTTVLSDADTAAPALAATAVAGTSKIVQAGGLLLRAVERTPPGHGRIAAPGLCTLAVLSSTTNDPAGSEGSDASGREAPILLPDDDTVTAATGRGTVVLETVTHTASRIAQRRLARRGLPLGSLFSRRLRWSLAGLLGCVLGMAVATWLTTDEHPLHAAYLTLLDLFAIGDPALDGPAARQVLQLLAGLAGLLLLPVLLAAVLEALGTFRTASALRRPPRGLSGHVVLLGLGKVGTRVLARLRELDIPVVCVEEEPEARGIPLARRLRVPTVLGDATQEGVLEAAKIHRAHSLLALTSHDTTSLEAALYARSVKPNLRVALRLYDDAFATAVYRTLRAAHPRALTRSRSVSSLSAPAFAGAMMGRQVLGAIPVERRVLLFAALNVAGHPRLEGRTIAESFRPGKWRVLALDTAEPDERLPDLAATPANHGVERPGGLVWDLHPGYVLRPEDRVVLAATRQGLAELLGRQPWLGTRTADA
>NZ_LN831790|2005371:2058129|2050724_2051447_-|WP_029386811.1|DBSCAN-SWA
MSPAVRSSRARAQLTLKEPPASVGAKPGGTIARLDLQFNPSTLELRKTTEWRRSPSRMAEESALPEFVGSGPRTLSLEVFLDATATHDNSVEQAVEKLMKACVPTPASLGRKKPASPWVRFEWGTARTTSFDGVLSSLSVTYTLFDVDGRPLRATCALTIEEASVDTPGQNPTSGARTARSTHTVVAGDSLALLAWREYGDATAWRVIAEANDIDDPMALAPGTELVVPGLRDAGAEEER
>NZ_LN831790|2005371:2058129|2026134_2027538_+|WP_029385200.1|DBSCAN-SWA
MSMSGARETGRRRLVVIGGDAAGMSAASQARRLKGPRELEIVAFERGHFTSYSACGIPYWVSGDVPGRDQLIARTPEEHRARGIDLRLRTEVTGIDVAGGRVRARDVDSGAESWTPYDQLVIATGARPVRPDLPGVDAPGVHGVQTLDDGEALLGTLARTRGRRAVVVGAGYIGVEMAEALIKRGYEVTVVNRAEEPMSTLDPDMGRLVGEAMEGMGITMVNGAEVTGLLTGDDGRVRAVVTRDAEFPADVVVLGIGVRPQTSLAAAAGLPLGSHGGLLTDRAMRVRGHENIWAGGDCVEVLDLVSGQMRHIALGTHANKHGQVIGTNVGGGYATFPGVVGTAVSKICDLEIARTGLREKDARRAGLRFSAVTIESTSRAGYYPGASPMTVKMLAEHRTGRLLGVQIVGREGAGKRVDIAAVALTAGMTVEQMTALDLGYAPPFSPVWDPVLVAARKAAAKVREAGV
>NZ_LN831790|2005371:2058129|2023469_2024933_-|WP_029385203.1|DBSCAN-SWA
MREEETPAGTGHVVVIGAGIAGLAAAHRLLERGARVTVLEASGRVGGKLLPGEIAGVRVDLGAESMLARRPEAVGLARAAGLADRLQPPATATASLWTRGALRPMPKGHVMGVPGTADALSGVLSEEGLARIERDAALPRTEIGDDVAVGAYVAERLGREVVDRLVEPLLGGVYAGDAYRISMRSAVPQLFEAARRHASLTEAVRALQGRTATAPPSGPVFMGIRGGIGTLPPAVARSVRARGGDIVTDAPVTELRRTAPTGWRVVAGERVLHADAVVVAVPAPAAARLLRAEAPAAAAELAAVEYASMALVTLAYRRSDAGALPEGSGFLVPPVDGRTIKASTFASRKWGWIAEQDPGLVVLRTSVGRYGETEILGRDDEGLVAVSRHDLKEATGLDAEPVAARVTRWTDGLPQYPVGHHARVARVREHVAALPGLAVCGAAYDGVGIPACVASAYAAVDQIHGDLRAVQELTAHPVQSLHGGAGE
>NZ_LN831790|2005371:2058129|2022733_2023465_-|WP_029385204.1|DBSCAN-SWA
MSDDASTPAPERIPNKGKLAKDLNEVIRYTLWSVFRLKDALPEDRAGYADEVQELFDQLAAKDVTIRGTYDVSGLRADADLMIWWHAETSDQLQEAYNLFRRTRLGRALTPVWSNMALHRPAEFNRSHIPAFLADETPRNYVSVYPFVRSYDWYLLPEEDRRRMLADHGKMARGYPDVRANTVASFSLGDYEWILAFEADELYRIVDLMRHLRASEARLHVREEVPFFTGRRKDIGELVAGLA
>NZ_LN831790|2005371:2058129|2020193_2020988_+|WP_029385263.1|DBSCAN-SWA
MFWVLLLLPAWVLAGTACARLCLTAVRTAATDTAGADAGGGRALTLYEAAFLSGGPGRVADLALVTMACRRQLLLAHTGWATVVDPRGRDEMERSVLGAIGPGGQSRIAPVRASAATADAVRGLAEHLVGAGLALPDGGRDSVAAAVRRVRLAALAVCALGAAAVALPVPMGTPRHLIALWFALPLLLTLGCLAVARMEIHPYARWASPAGQRLLCALPRQSGGADGERTFLTSVALRGVHAIGEPDLRAAFAHRERHAGRYGS
>NZ_LN831790|2005371:2058129|2029051_2030587_+|WP_029385197.1|DBSCAN-SWA
MSLDSITTSVDKAVSGFFEPIATWLVEVIFYAVPVGGTDLPLIVAWLVVAGLVFTGWFGFVQLRKFKLAVDVVRGKYDEKGAAGEVNHFQALTAAVSGTVGLGNIAGVAVAVSIGGPGATFWMILCGLLGMATKFVEVTLGVKYREVHADGTVSGGPMHYLPKGLAERFGKNGKTLGKILAVLASFFVLFFGLFGGNLFQVNQSYAQLVSVTGGEDGLTGSSAGALFFGILIASLVGIVLLGGIRSIANVTSKLVPAMAGIYIAACLVVILVHVTSVPAAIVTIIEGAFNPQGVAGGVLGALIIGFKRAAFSNEAGLGSAPIAHSAVKTKHPASEGLVALLEPFIDTVVICTMTALTIVIANPASWGEARKGESIGGVTITSDAFATVMPWFPYILTVAVLLFAISTVLTWGYYGLKAWTHLFGRSRTSELVYKVVYTLFAIAGSLLTLQTLIDMADAVLFMLAVINIIGLYLLAPVVKRELNSFLEFVRTRNAGEITEDDKDQESVKTTV
>NZ_LN831790|2005371:2058129|2048012_2048435_-|WP_029386814.1|DBSCAN-SWA
MSDRFIGRGWAFPMRVGPTGGIALVEREREIEEAIRLVLATAPGERPMRPEFGCGIHDYVFAPGDGATAGRVAQQVREALERWEPRIAVDDVVVAYDTVEAGTLYIDVHYTVRSTNDRRNLVFPFYTIPSDEGGGERGAA
>NZ_LN831790|2005371:2058129|2052145_2054041_-|WP_166520571.1|DBSCAN-SWA
MPPAVLPAPGDRADGGTAAPSPAGAVAPATGPAQRTARSAEDRAPLGAPLNALPATALPATDLPTADGSTRPSAPAARSAAGAPAASGPALPVVQRHAQDGAGTPGPHDVGEGRTAHGGPAARAGATDPASGTGRGGARARGGLGAPLSALPPSAELPRSAASGRPAPPTGYGPDVQRAPARPDGGADTASAASRTDGGRTAAPRTAPGAAPPPSSAGSPPGGAEHSPLLGTREVQRLAGPAAEGAARPGSADPGQDSARPLVKPSSDGAARPASREATGAVAAAADPRGARPATVRGPGGQPPREPVVPVRPVSAARPVHGGASGAGVRTGAGAAPSPDAAGRGALTVSRAPVLPVPAAPRTLPLLAARPLRTETRLPEGAAPPVASRPGGRPVVAARWTGAPAGVSAAPRSGTTPHPGPAPGAATPSAPPGVRSAAVRPGPAAAGTGRAASAGSGRGVPVVRPAPHRGGTPGTTVQPAAAPARSLPVAGARTPAPTGPAAAAVPPAPPASVPVVRPRAVPAGPGPATGGEKGPVAPVVQRKAAGTAQAAGGAPPAGPRSASPPSASGTPVSRTSASGTAHRAGAPPDPGPDRDDLDDLARRLLDPVSRLLRAELRRGRERMGRPHDRRR
>NZ_LN831790|2005371:2058129|2048904_2050728_-|WP_029386812.1|DBSCAN-SWA
MSTAEAQGGRSFAADPVVEAPAELPKIWAAQLVSCVVDENVGLPDAAVLTFRDPDHEFLRATGITIGTPLRVSVVTVSGRARERLFNGEVTALEVDRDSTGSFTVVRAYSKAHRLQRGRKVVAYRNMTAAAIVRKVAAGAGLACGTVEAAPVSYRQLSQANVSDWEFLQYLAGESGAQVRVDDQGVLQFTRPEKAAGAPAPSTSATRDPMVLEYGRNLLALRAALSAADGAASVEVRGWDVTTKKPLVARQPSVVSDTVVPGLSPQTGARFGASAKLAVTDTPYRTQAETTAAAGAMAAQVSAGFGELEAVAEGNPRLRAGKPVALGNVGPAFSGRYTATAVRHVLEPYGGYRTTVWVSASPDRSLTGLVTGANAPGRGPRMPGLAIGVVTDVREPGGAERGEVRLRFPWLDDTYTTDWVRTVQWGGKGGGGVVSPEVNDEVLVGFEQGLLDSPYVIGGLYNGVDRPSPHDVPLVDATSGRVNRRSVVSRSGHRVELLDARAPGPSGLRLTTGDERLEVRLDDRRDRIELTVYAGRGRPLTSVLLDRDGITLDAGRGDVTVRGRRVEIDATDTVTVGGRSVRVTGQTEATVDGGLLGVLKARLIKIN
>NZ_LN831790|2005371:2058129|2040519_2040885_-|WP_029385187.1|DBSCAN-SWA
MMSNRRPGGALAAVLIAAAATSTFSHPAQAAPEAAPKAPTQATPTCYATSCHGLDPIETHCVDDAVTIDDAAHEGRIVRLRYSAQCRAAWVQLWFGKPDDRAYVRTEENSSPEWAKSSGGG
>NZ_LN831790|2005371:2058129|2055460_2055619_-|WP_164497197.1|DBSCAN-SWA
MTYALPRLREEIAYIAYHFHWQREEILDLTHGERQQWVAEIARINTRINESG
>NZ_LN831790|2005371:2058129|2056581_2058129_-|WP_029386829.1|tail|DBSCAN-SWA
MPTYLTPGVYVEEVQSGARPIEGVGTAVAAFVGFAEAGPFHTPTLVTSWDQYTQLFGGFTEGTYLAHAVYGYFANGGGAAYVVRIGGSAEDASAPAADGTGRGQQAGAPRPVELGGFLVAARPGAVGVSVEIADVPGEDPPEDRFRFLVRQGGEVVETFDASTRKSVKGYLVSQARNSKLVEVTERRDAPQARPAAQTVALPDAPAAPGAVARLDPSEYVGDAAARTGFGGLETIDEITMVAVPDLMSAYQRGDIDAEGVRTVQLAVISHCEQMGDRVAVLDTPPGLTAQQARTWRNDEAGYDSRYATLYYPWVRVFDPAAGRNTTVPPSGHIAGVWARSDAERGVHKAPANEVIRGAVDLEIRLSKGEQDLLNPIGVNCVRAFPGRGVRVWGARTLSSDPAWRYLNVRRLFNYLEESILLGTQWVVFEPNDDRLWSSIRRNVAAFLTEEWRRGALFGRTAEEAFYVKCDRDNNPQESIDQGRVVCEIGVAPVKPAEFVVFRLAQFSDSTSLIDE
>NZ_LN831790|2005371:2058129|2014389_2014752_+|WP_047122429.1|DBSCAN-SWA
MDLANSPNLEEVFGQAPLRPRFYSISGITAATKWWRDELDEETLQCYLGTSEEHAAPGHMSRMKTVIIGDLGPDLPFVLDYRDSFADPSVAFLGEGDAWRRVSDNVRALLAMLDGQRPDA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_029387628.1|2005371_2006082_+|tRNA	peptidyl-tRNA hydrolase	NA	NA	NA	NA
WP_029387627.1|2006119_2006941_-	APH(3'') family aminoglycoside O-phosphotransferase	Q75ZG1	Hepacivirus	2.4e-26	37.1
WP_079164117.1|2007445_2014306_+	Rhs family-like protein	NA	NA	NA	NA
WP_047122429.1|2014389_2014752_+	hypothetical protein	NA	NA	NA	NA
WP_029385269.1|2015101_2015401_+	hypothetical protein	NA	NA	NA	NA
WP_029385265.1|2018689_2020087_+	DUF692 domain-containing protein	NA	NA	NA	NA
WP_029385263.1|2020193_2020988_+	TIGR04222 domain-containing membrane protein	NA	NA	NA	NA
WP_047121666.1|2021116_2022733_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_029385204.1|2022733_2023465_-	chlorite dismutase family protein	NA	NA	NA	NA
WP_029385203.1|2023469_2024933_-	protoporphyrinogen oxidase	NA	NA	NA	NA
WP_029385202.1|2025091_2026024_+	DUF4349 domain-containing protein	NA	NA	NA	NA
WP_029385200.1|2026134_2027538_+	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_029385198.1|2027593_2028403_+|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_029385197.1|2029051_2030587_+	alanine:cation symporter family protein	NA	NA	NA	NA
WP_029385196.1|2030913_2031975_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_029385195.1|2032186_2033716_-	flotillin family protein	NA	NA	NA	NA
WP_029385194.1|2033821_2034337_-	hypothetical protein	NA	NA	NA	NA
WP_099053772.1|2034744_2036649_+	NAD-binding protein	NA	NA	NA	NA
WP_029385192.1|2037253_2037631_+	hypothetical protein	NA	NA	NA	NA
WP_029385190.1|2038282_2039734_-	MFS transporter	A0A0M3UL24	Mycobacterium_phage	8.6e-11	25.8
WP_078648312.1|2039845_2040364_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_029385187.1|2040519_2040885_-	DUF2690 domain-containing protein	NA	NA	NA	NA
WP_048574340.1|2043292_2043922_+	hypothetical protein	NA	NA	NA	NA
WP_166520570.1|2043999_2045490_-	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_029386816.1|2045494_2046058_-|tail	phage tail protein	NA	NA	NA	NA
WP_029386815.1|2046054_2048013_-|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_029386814.1|2048012_2048435_-	GPW/gp25 family protein	A0A1D8KT65	Synechococcus_phage	9.9e-08	32.3
WP_029386813.1|2048431_2048752_-	PAAR domain-containing protein	NA	NA	NA	NA
WP_029386812.1|2048904_2050728_-	VgrG-related protein	NA	NA	NA	NA
WP_029386811.1|2050724_2051447_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_029386810.1|2051568_2051994_-|tail	phage tail protein	A0A059XEM3	uncultured_phage	4.6e-05	28.3
WP_166520571.1|2052145_2054041_-	hypothetical protein	NA	NA	NA	NA
WP_164497197.1|2055460_2055619_-	hypothetical protein	NA	NA	NA	NA
WP_029386827.1|2055615_2056110_-	hypothetical protein	NA	NA	NA	NA
WP_029386828.1|2056106_2056547_-|tail	phage tail protein	NA	NA	NA	NA
WP_029386829.1|2056581_2058129_-|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	1.1e-69	35.5

2. NZ_LN831788

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	5147 : 14597	12	Brevibacterium_phage(25.0%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_LN831788|5147:14597|DBSCAN-SWA
GATGGCACTCGTCCCTGTACCGATCGCGACGCTGGGCGCGGAGCACTCAGCGCAGCAGTTCCGCATGATGATCAAGGATTTGGCGCGGGACAACCAGGGCGTCACCACCGGATCAGACTTGAAGGTCACCGCTCTCGCGACGCCGGGCGGCGCCGTGCAGATCGGCGACGGATCCGCGGTCATCGCCGGGAAGGTCTCCCCGGTCCAGGGCTACTACAACGCGTACAACATCGGCTCCGACACCGTGCAGATCGCTGCGACGGGCAGCACGTCCCGCTCCGACATGCTCGTGCTGCGCGTCGAGGACCCCGAGTACGAGGGCGACCGCGACCCCGCTACGGATCCGATCGTGTTCTTCGAGGTCATCCCCAACGTTTCCTCGACCGCGACGACGGTGCCGGCCGGGTACTCGGCGATCCCGCTCGCCCGGATCGACATCCCATCGTCCACTGCCACGATCACCAACGCGATGATCAAGGATCTGCGGCAGATCGCGAACCCGCGGCGGGAACGGATCCTCACCCCCTACTACTTTCCGGGCCCGTTGCAGGAGATATCTGGGACATCCACGACGTGGAAGACCCACCCGAACGTGACCATGGCGACGCTGGCCATCCCATCGTGGGCGGCCACCGCGAAGGTCGTGTTCTCGGCGACCAACATCCGGCTTGCCGAAGGCGCGATCTTCGCCGGGTTCCGGTTCATGCTCGGCAGCACCGAAGCCGTCCAGGAAGTCCGCATCGACGACAACCAGGGCACCTCGGCCCGCCGCGTCTACGTGGAGATCGTGGAGACGATCGATCTGACCACCACAGCCGGGGCGGCGATGCGCGGCACCAACCAGCCGTTCCGCGCTCGGATGCGCACCGACGCCTTCAATGACGGAAAGATCGGCGCCGACTCCCTGACCAGCTACAAAATCGACGTCGAGTTCCTCGAGGGCCGCCTGTGACCAGCCGCTGGCGGTACTGGACCCAGCACGCCCTGACCGGGGTGATGCTGCACCCCGCGCTGCCGCTGACCGACGTCGAGTTCGGCAACGAACTCAACGGCCCAGGTGAGCTCCGCGGCACCCTCACGCCCCGCTTCGTGAAAGCCAACGCGGCGTCGCTGCTGCCGGGCAAGGCCCTCATCTACGCCGAAGCCGACGGCATCCTCCGCTGGGGCGGCCTCATCTGGGACGTCACCGTCGAGGACGGTGAATACCGCCTCGAGGCCGCGTCCTGGTCGTCGTACCTGAACGCCCGCCACGACCACCACGGCGAGCTCGCCGGCCGCGGCCCCTACGTGAACACCGACCCATGCAAAATCATCCGCGACATCTGGGCCTACGCGCAGTCCCAGCCCGACGGCAACCTCGGCGTCACCGTCGACACGACGACGTCGAGCATGAAGGTCGGCACCCCCGCAGAGCCCTGGCACTCCTACTGGTACGAGACGCCCAACCTCGGCGACCAGGTCGACGACCTCATCTCCGAGGACGGCGCCCCCCAGTACACGAACACCTGCCGCTACCTGGCCAACGGCACCGTCGAGAGGCGCCTCAAGCTGGGCTATCCGCGGCTGGGTGCCCGTCGCACCGACATCAGCTTCCGCACCGGCGTGAACATCGTGACCGCGCCGCCGGTGGAGTACTCGGGCGACGACTACGCCAACGTCATCCTCGCCACCGGCTCCGGTGAGGGAACCGCCACCCGCCGGGCTGAGGCGCCGTCCCGGGACGGGGGGCTGCGCATGGAGCATGTTCTGGCCCTGCCGACCGTCAACGGCAACGACATCCTCGCCAAGCGCGCCGCGGCGGAGCTGAAACGCCGCAAGATCATGGGCCAGGTCGAGACGATCACCGTGCGGGACCATCCCAATGCGCCCCTCGGGTCGTGGCAGATCGGCGACGACGTGACCGTCACCGTCAACAACCAATGGGTGTCGTGGTCCGGCTGGGCCCGGGTCGTCGCCGAGTCCTACCAGCCCGACAAGGCGCCCGACCAGGCCGTCCTCACCCTGAAACGCGCCGACTCCTACCACTACGGACCCCCGGAGGCAGCCTGATGGCCCGCAGCATCCCCCAGGAGCTCGCCCGCCTCGCCCGCGAGCTGAAGGAGATCAAGAGAGGGCAGCGGTACGCGCACGGCGGCAGCATCGAGAACAGCGCGGTCGAGGTCAAGGACGGCACGGGGAGTCTCCGAGCGATCGTCGGCGTGCAGGCCGACGGGACCACCGCCGTGAACATCGTGAACGGGCCGCCGCCGCCTCAGCCGAGCCCGCCGATCGTCACCCCGGTTCTCGGCGGGGTCGCCGTCTCCTGGGACGGCGCCTTCGCTGATGGTGCCGTGCTGCCGCTGGACTGGCAGCGCATCGAGGTACACGCCTCCGCCATCGACGGCTTCACCCCCGTCCCGGACACCCTCCACGGCACCATCGAAACCCCGCAGGGCAGCACGGTCGTCGCCGCCACCGACACCCCCGTCTACGTCCGGCTGCTGGCCCGCAGCACCTCCGGTACCGCCTCCACGCCATCCGCTCAGGCTGGGCCCGCCGGCCCGGCGCCGGTCGTCGCCCAGGAACTCCTCGACGGGATCGTCACCAGCAGCAAAATCGCCGCCGGCGCGGTCACCATCAACGCGCTCACCGAATCCCTCGCCGACACCGCCTCCCAGCGCTACGTCGATGCCATGGGCGACCCGACCGCGTGGACCGTCCTCACCAAAGCACCAGCCGCGACCTGGACCTTCCTGGACGGCGTCACCGACGCCCGCACCGGCAGCACCGTCGCCCAGGCCACCGGCTACACCGTCGTCCGTGGCACCCTGCAGATGCCCTACGACCCCGACGTGCTGTACCGGGTCTCCGTCCGGGCCCGGACTACAGCCGCGTCCGCGTCCGGCACCGACACCCTGTACGCCGGCGTCCTCGGCATCGCCGCGGACGGCGTCACGTACGTCAACCGGACCGGCGCCAACTCGTACTACACCCAGCTCTACCCGGCCGCCTCGAACACAGCGCAGCCCACCGCCTCGGGCTGGGTCACCTACACCGGCTACCTGAAAGGGCACGCCGCGTCCGGGACCGTCGGCACGATGCCGGATCCGCGCACCCCGGGCGCCGCCCACACCAACGTCCGCTTCCTCGCCCCGCTGCTGTACCTGAACTTCGGCTCCGGAACCTCCGGCGACACCGGCACCATGCAGGTCGACGCGTTCACCCTGGAAGCGCTGAAGACCGGCGTCGTGAACAGCAGCAACCTCGTCGCCGGGTCGGTGACGACGGCCGCGCTCGCCGCGGACTCGGTCACCGCCACACACATCCAGGCGAACGCCGTGACGACAGCTAAGCTCGACGCGGAAGCCGTCACCGCAGCGAAGATCGCGGGCCTGACCATCACCGGCGACAAGATCGCCGCGAACGCCATCACCGTCGGCAAGCTCGCCGCTGGCGCCGTGGACGCGACCGCGCTCGCCGCGGACGCCATCACCGGCAAGACCATCACCGGTGGCATCATCAACGGTTCCCTTATCCAGACCGCGACCAGCGGGCCCCGGGTCACCGTCAACGAGGACAACCTCAACAAGGTCCTCGTCTACGACGCGACCACCCCCACCGCGATCGGGGAACTCTCCGAGCGGGGCCTGCTCCTCCAAGGCAACAACGGCGCAATCCTCTGGCTCGACCCGGACAGCGCCTATCCGAACCTGCGGTTCACGAACGCGGCTCAGACGAACAGCGCCTACGTCAACGTGTCCGAGACCTCGCCGGGCGCCGCCGACCTCGGCCTGACCTCCGGGGTGTTCACCGGATCCGGGTTCTCGGACATGAAGTGGCGCACGTTCATGGGTAACGATTTCGCGGTCATCGAGCGAATCAGGAACGCTGACGATCAGTACTCGGTGGGTGGGCGTTTCTTCCTCAGCGGCACCTCCGCCTCTCTCGGCTACCGCGACTCCGGCGGCACGTCCCAGAGCAGCACGCTCTTCGTGCAGGCTGGGCACGCTTTCGTCAGCGGCGGACGGTTCAGCGTCCAGCCCCCCGCATCGTCGTCCAGCGCTGTCCTCGTTAGCGTGGCCGCCGGGCACACAGGCAACCTGCTGAACCTCACCGTTGACGGTGCCACCAGGATGAACGTCGACAAGGACGGCAACACTGACATCAAGGGCATCATGACGGCCGGGAACATCGCGTCCGGCACCATCACCATCACCCCCTCCGCCGCCCACACCCCGACCAGCGCCAGCGTCAACTTCGGCCCGCTGAAGGGCACTACTTTCCGCGGCTACGCCACCGCCGTCACCACCGTGCCCGGCGTCCGCACCCCGGTCGGCGCCCAAGGCGTCACCGGCGTTTCCGTCTCCTCGGTTACTTCCAGCAGCATGCTGGTCTGGGTCAACCGGGAGAACACGACCGCAACCGTCATCAACTGGATGGTGATCGCATCATGACCGAGTCCGCGTCCGAATCGACACAGAGCACCGAGCCGCCCCAGCCCCCCGAAGGGGATCCGCCGCCCGAGCCGGTCGACCCCGACCCGGAGACCCCGGATCCGATACCCGACCCGGAGCCCATCACCTGGGAGCCGCAGACGTGGTACGCCGTCACGGCCGCGTGCCGCACCCCCGGATGCCGGCAGGAGAACATCGTCGTCGACATCCCGATGTTCTACTCCAACAACGGCGACCCCAAGTTCTGTCGCGTCGTGTGCGCCCAGGACGGCGCGTGCGGCAAGGACGCCACGATCCTCACCGCGAGCAAGCTGGACCCGCAGCCGCCGGAGGAATGAGCAGCCAGGCGGGGGCAACAGCCCCCGCCGCAGGCCCTAGCCTGATCACAGGGGCGACCCTCCGCCCCGAGCAGCACCCCTCCGAGGGACGGCCGCAGCATGTGGCCCGCCATCACAGTTCACCTGGGCGCGGGGAGATCCAGGAGACCGGGCGATGCCCGATCCGAGCACACCACAGGACGAGTCGACGACTGCCCGGAAGAAGACCGCCGCAGCCCCGGAGCTCGAGCCGGCCACCGACACCACCACGGCATCCGACACCAGTACTACCTACGAGCCGTACCCGGGCGCCGGATTCTTCCACGGCGGCCGCCACTCCCAGGTCTTCGTGGCGATGGCCGCCCGCCTCGAGGTCGAGGGCTGCACCGACGGCCGCTACCTGGGCCCGGACTGGACGAACGCCCACCGTGACGCTTTCGCTGCCTGGCAGCGCACCCTGCGCCCCAAGGAGGGCGGCGACGTCTCCGGCATCCCCGACCAGGTGGCCTGGGACCGACTCCAGGTCCCGCGCGTCAGCCCCATGACCGGGGAGGCGTCCTGATGGCCAAGCCACTGTCCGCCGCCGACTTCCTGGACTGCCTCCGCGACGAGGGCCTGAACGTCGTCGAGGTCGACGCCTGGGAGACCCACAACCGCAACAGCAAGGGCCCCTGGGGTCCCCTCCACGGCGTGATGATCCACCACACCGTCACCCGGGGCAGCAGCACCACCGTCGAACTGTGCCGCAAGGGACACAGCAGCCTCCCCGGACCCCTGTGTCACGGCGTCATAACCAAGGACGGCACGGTCCACCTCGTCGGATACGGCCGCGCTAACCACGCCGGCCTGGGCGACCCGGACGTTCTGGCCGCGGTCATCGCCGAACGGCGACCGCCCACAGACAACGAGGCCACGGTCGACGGCAACCGGCACTTCTACGGCTTCGAGTGCGAGAACCTCGGCGACGGCAAGGACCCGTGGCCCGACGAGCAGATCGAGGCGATCGTCCGCGTCATCACGGCGCTGGGCCGCCGCCACGACTGGGCGGCCCGCTCCGCGCTCCGGCACCTCGACTGGCAACCCGGCAAGATCGACCCCCGCGGACCGCAGTTCGACTGGGACGACATCCTCAGCCGAGTGGCGAAGCGACTGGCCGGGGCCACGCCCAGCAAGCCGACACCCCCCGCGCCGAAGCCGCTGCCCACGCCGAGCAAGCCGGTCGTAGACCTGTCCAAGCTGGTCGCCGCCGCTCGGTCGAACCCGGCGGCGAAGGGCCAGCCCGTCACCTACTCCGGCGTGAGGACCGTCGAGGCCGCCCTGGTCGATGCGGGCCTGCTGAGCAAGCGGTACAGCGACGGACACTGGGGCACCACCACGATCACCGCCTACGCCGCGTGGCAGCGCAAGCTCGGCTACCGCGGCAAGGACGCCGACGGCATCCCCGGCCGGACCTCCCTGGAACGCCTTGGCGACAGGTACGGATTCACGGTCACGGCATGAGCGCCCGCCGCGCCGCGCTCGTCCACTACTGCCTGGCGGGCGTCTGGGCGCTGCTCGTGATCCCCACCCTGCTGTTCTGGAAGAACAGCGTCCTATGGGTGGCTGCGATGTCGCTGTACGCGAACTTCGTCGGACATCTCTCCGCGGCAAAGGCAAGCCGCGCCGAACAGGAAGCGCAGAAATGAAAATTCTTGGCCGAGAGCCCGCCCTGCTGCTGGGCCTCATCGCTGCCGGCGTGAAGATCCTCGGGTACGAGTTCGACGTGTCCGCTGGCGTCCAGACCGGCATCAACACCGTCGCCGCCGCCGTGGTCGGCCTGATCCTCGCGGTCCTCGCCCGCAACGGGGCCTGGGCGGCCGCTCTCCTCCAGACCGCGCAGGCCGTCATGAGCCTGTTCGTCGGTCTCGGGCTGGACTGGTCCGCGGACCGGCAGGCGCTGTGGATGGGCGCCATCGCCGCGGCTGTGGCAGTCGTGGAGCGGTTCATGGTGACGCCGCCGCTGCCCACCACGCCGCTGGAGGAATCGAGCCCCCTGGCGAAGCCGCACGGCCCGCGGGCCGTCTAACCCACCCGTACCCGGAGCAATCAGTGGCTGACGAGCCGACCCTGGGCGAAGTCCAGCGCCGCATGGAGCAGGGGTTCATCGACCTCAAAGACGACATGCGGGAACTCGGCGTGCGGCTCGACAGCAAAGTCGATCAGAAGGTCTACGACCTGCGTCATGAGGCCCTGGCCGCCAGGGTGACGACGCTGGAGACCCTTCGCGAAAAGGACGCCGAGAAGATCGTGGCGACCCGCCGATGGCTGGTGGGCGCCGTGATCGTACCGCTCATCGGGATTCTTCTACCGGTGATCATCCTTCTGGTGCAGGGGTCTTGATGTCAGGGACAGGGGCACAAATACGAGCCGAGGAACGCCGCTGGCGCCGCGGGGACATCTTCACGGTCGCCATCGCAGTCTTCCTCGGCCTGGCCATGGCCTGGATCGTGCTGTCGGTTCAGCAGCTGCGCAGCGACCTGAAGGTGTCGAACGAGGCCCGGGACGCTCTGGCACGGCAGGTGCTGGAGCTGGGTGAAAAACCGGTGACCAGTGAGTCCCAAGGCCGCTCCGACCCGAGTAAGCCTGTGCCCGGCCCGAAGGGCGATCCAGGTTCGCCCGGCCCTTCCGGCCCCGCCGGTCGTGCCGGCGCTACGGGCCCGTCCGGTAGGCCGGGTGCGGACGGGCGGAACGGTGTGAGCACCACAGGCTTGCCGGGGCCGCCCGGTCAGGATGGGGCGCCTGGCCAGCCCGGCACGAACGGCCAGCCCGGCGCTGACGGACAGCCCGGCCCGCCTGGGCCCCAGGGAGAGCCGGGGCCCCAGGGAGAGCCAGGGCCAGAGGGCCCCCAAGGCCCTCCCGGACAGGACGGCAAGGACGGTCAGACCTGCCCCGACGGGTACAGCCTCCAGGCCCCGGCAGACGACCCGGACGCGCTCGTATGCCGCAGAGACGGCGCCCCCCAGCCAGAGCCGCAGCCGTCCCCGCAACCGACCGTCCTCGGCGTGGCTCCCGAGCGCCGACGGGCATAGTCCCCGACTCTGGCCGGATGGTCATGGGGCGACGCGGCCGTTGGCGTTGAAGGCGGCGTACGTGAGGGGCATGAGCCTGGCCCACTCGGCCTCCATCTTCTCGCCGACCATTTCGATCTCCCGCTGCGGGAAGGAGGGCACCTTCGCCAGCTCGTGCTGGGTGCGCAGGCCGAGGAAGTGCATCAGCGAGCGGGCGTTGCAGGTGGCGTAGGCCGACGAGTACAGCCCGACGGGGAGGACCGAGCGGGCGACCTCCCGCGCGACGCCCTTCGCCAGCATCTCCTGGTAGACGCCGTAGGCGATGGAGTACGACATCCTCATCGCTTCCTGGGTGATCCGGTGCTGTTCCGGGGTGCCGTCTACGAACCGGTACCGGCCGGGCTTCCCGTCCTGGACGAGCTTGCGGTCCGGGCCGGGGATGTAGAAGACCGGCTGGAGCTCCCGGTAGCGGCCGGACTCCTCGTTGTACGACCAGCCGGCGCGGTGCCGCATGAACTCGCGGAAGACGAAGATCGGAGCGTTGATGAAGAAGGTCATCGAATTGTGCTCGAAGGGGCTCCCGTGCCGATCCCGTATCAGGTAGTTGATCAGTCCCTTGGAGCGCTCCGGGTCCTTGTTCAGCTCGTCGAGCGACTGCTCCCCGAGCGTGGAGACGCGGGCCGCGAACAGTGCGTCGGCGTCGGACGCGCTGTGCTTCACCAGCTCTACGGTGACGTCGCTGCGAAAGACGGGCTCGGGCGTGGGCGCCTGGTCGGGCATGGGAAGGGCTCCGATCGAGGGGAAGGGCGGTACCTCCAGTGTCCCGGCGCCGCGGCGCGGTGTTCCCTCCGCACAGTCGTACGATGACAGCGTGAGCACCACCCCTGACAGACCCGTCCCGCCGGCCCCGGAGTGCGCCCCGTCGTACGTGGGGCCGTGCACGAAGTGCCAGCATCCGACGCACCGCTACGGGCCGGGCGGGAACCCGCTGTGTGTGCTGTGCCGACGGGAGCTGGAGGAGTGGCGGGCATCCCAGGGGAAGGCGACGTCGGGCCGCGTCTAGGCTTCTGACGTGCTCCTTTCCGATAGAGACCTCCACGCAGCGATAGCCGGCGGACGACTCGGCGTCGCCCCGTACGACAAGGCGATGCTCCAGCCGGCCAGCATCGACGTCCGTCTCGACCGGTCCTTCCTGGTCTTCGAGAACCACCGGCATGCCTGCATCGACCCCGCGGTGGAGCAGGACGACCTGACACGGCTGGTGGAGGTCGACGACGGGGAGGCGTTCGTGCTGCACCCGGGCGAGTTCGTGCTGGCGTCCACCTTCGAGCGGGTGCGGCTGCCGGACGACCTGGCGGCCCGGCTGGAGGGGAAGTCGTCGCTGGGGCGCCTGGGTCTGGTGACGCACTCAACGGCGGGGTTCATCGACCCCGGGTTCGAGGGGCACGTCACGCTGGAGCTCAGCAACCTCGCCACCTTGCCGATCAAGCTGTGGCCGGGGATGAAGGTCGGGCAGCTGGCCGTCTTCACACTCAGCTCGCCCGCTGAGGCGCCTTATGGCACGAAGGGCATCGGGTCTCGGTACCAGGGGCAGCGCGGGCCCACCGCCTCCCGGTCCTGGCAGGACTTCCACCGGACCGCCCTGCCATCCTGA

Protein sequences of DBSCAN-SWA_1

>NZ_LN831788|5147:14597|6094_7195_+|WP_047121226.1|DBSCAN-SWA
MTSRWRYWTQHALTGVMLHPALPLTDVEFGNELNGPGELRGTLTPRFVKANAASLLPGKALIYAEADGILRWGGLIWDVTVEDGEYRLEAASWSSYLNARHDHHGELAGRGPYVNTDPCKIIRDIWAYAQSQPDGNLGVTVDTTTSSMKVGTPAEPWHSYWYETPNLGDQVDDLISEDGAPQYTNTCRYLANGTVERRLKLGYPRLGARRTDISFRTGVNIVTAPPVEYSGDDYANVILATGSGEGTATRRAEAPSRDGGLRMEHVLALPTVNGNDILAKRAAAELKRRKIMGQVETITVRDHPNAPLGSWQIGDDVTVTVNNQWVSWSGWARVVAESYQPDKAPDQAVLTLKRADSYHYGPPEAA
>NZ_LN831788|5147:14597|10071_10458_+|WP_053042657.1|DBSCAN-SWA
MPDPSTPQDESTTARKKTAAAPELEPATDTTTASDTSTTYEPYPGAGFFHGGRHSQVFVAMAARLEVEGCTDGRYLGPDWTNAHRDAFAAWQRTLRPKEGGDVSGIPDQVAWDRLQVPRVSPMTGEAS
>NZ_LN831788|5147:14597|11984_12275_+|WP_047121231.1|DBSCAN-SWA
MADEPTLGEVQRRMEQGFIDLKDDMRELGVRLDSKVDQKVYDLRHEALAARVTTLETLREKDAEKIVATRRWLVGAVIVPLIGILLPVIILLVQGS
>NZ_LN831788|5147:14597|11577_11961_+|WP_047121230.1|DBSCAN-SWA
MKILGREPALLLGLIAAGVKILGYEFDVSAGVQTGINTVAAAVVGLILAVLARNGAWAAALLQTAQAVMSLFVGLGLDWSADRQALWMGAIAAAVAVVERFMVTPPLPTTPLEESSPLAKPHGPRAV
>NZ_LN831788|5147:14597|9575_9917_+|WP_047121227.1|DBSCAN-SWA
MTESASESTQSTEPPQPPEGDPPPEPVDPDPETPDPIPDPEPITWEPQTWYAVTAACRTPGCRQENIVVDIPMFYSNNGDPKFCRVVCAQDGACGKDATILTASKLDPQPPEE
>NZ_LN831788|5147:14597|7194_9579_+|WP_053042656.1|DBSCAN-SWA
MARSIPQELARLARELKEIKRGQRYAHGGSIENSAVEVKDGTGSLRAIVGVQADGTTAVNIVNGPPPPQPSPPIVTPVLGGVAVSWDGAFADGAVLPLDWQRIEVHASAIDGFTPVPDTLHGTIETPQGSTVVAATDTPVYVRLLARSTSGTASTPSAQAGPAGPAPVVAQELLDGIVTSSKIAAGAVTINALTESLADTASQRYVDAMGDPTAWTVLTKAPAATWTFLDGVTDARTGSTVAQATGYTVVRGTLQMPYDPDVLYRVSVRARTTAASASGTDTLYAGVLGIAADGVTYVNRTGANSYYTQLYPAASNTAQPTASGWVTYTGYLKGHAASGTVGTMPDPRTPGAAHTNVRFLAPLLYLNFGSGTSGDTGTMQVDAFTLEALKTGVVNSSNLVAGSVTTAALAADSVTATHIQANAVTTAKLDAEAVTAAKIAGLTITGDKIAANAITVGKLAAGAVDATALAADAITGKTITGGIINGSLIQTATSGPRVTVNEDNLNKVLVYDATTPTAIGELSERGLLLQGNNGAILWLDPDSAYPNLRFTNAAQTNSAYVNVSETSPGAADLGLTSGVFTGSGFSDMKWRTFMGNDFAVIERIRNADDQYSVGGRFFLSGTSASLGYRDSGGTSQSSTLFVQAGHAFVSGGRFSVQPPASSSSAVLVSVAAGHTGNLLNLTVDGATRMNVDKDGNTDIKGIMTAGNIASGTITITPSAAHTPTSASVNFGPLKGTTFRGYATAVTTVPGVRTPVGAQGVTGVSVSSVTSSSMLVWVNRENTTATVINWMVIAS
>NZ_LN831788|5147:14597|11392_11581_+|WP_047121229.1|DBSCAN-SWA
MSARRAALVHYCLAGVWALLVIPTLLFWKNSVLWVAAMSLYANFVGHLSAAKASRAEQEAQK
>NZ_LN831788|5147:14597|14015_14597_+|WP_047121233.1|DBSCAN-SWA
MLLSDRDLHAAIAGGRLGVAPYDKAMLQPASIDVRLDRSFLVFENHRHACIDPAVEQDDLTRLVEVDDGEAFVLHPGEFVLASTFERVRLPDDLAARLEGKSSLGRLGLVTHSTAGFIDPGFEGHVTLELSNLATLPIKLWPGMKVGQLAVFTLSSPAEAPYGTKGIGSRYQGQRGPTASRSWQDFHRTALPS
>NZ_LN831788|5147:14597|10457_11396_+|WP_047121228.1|DBSCAN-SWA
MAKPLSAADFLDCLRDEGLNVVEVDAWETHNRNSKGPWGPLHGVMIHHTVTRGSSTTVELCRKGHSSLPGPLCHGVITKDGTVHLVGYGRANHAGLGDPDVLAAVIAERRPPTDNEATVDGNRHFYGFECENLGDGKDPWPDEQIEAIVRVITALGRRHDWAARSALRHLDWQPGKIDPRGPQFDWDDILSRVAKRLAGATPSKPTPPAPKPLPTPSKPVVDLSKLVAAARSNPAAKGQPVTYSGVRTVEAALVDAGLLSKRYSDGHWGTTTITAYAAWQRKLGYRGKDADGIPGRTSLERLGDRYGFTVTA
>NZ_LN831788|5147:14597|12985_13723_-|WP_047121232.1|DBSCAN-SWA
MPDQAPTPEPVFRSDVTVELVKHSASDADALFAARVSTLGEQSLDELNKDPERSKGLINYLIRDRHGSPFEHNSMTFFINAPIFVFREFMRHRAGWSYNEESGRYRELQPVFYIPGPDRKLVQDGKPGRYRFVDGTPEQHRITQEAMRMSYSIAYGVYQEMLAKGVAREVARSVLPVGLYSSAYATCNARSLMHFLGLRTQHELAKVPSFPQREIEMVGEKMEAEWARLMPLTYAAFNANGRVAP
>NZ_LN831788|5147:14597|5147_6098_+|WP_047121225.1|DBSCAN-SWA
MALVPVPIATLGAEHSAQQFRMMIKDLARDNQGVTTGSDLKVTALATPGGAVQIGDGSAVIAGKVSPVQGYYNAYNIGSDTVQIAATGSTSRSDMLVLRVEDPEYEGDRDPATDPIVFFEVIPNVSSTATTVPAGYSAIPLARIDIPSSTATITNAMIKDLRQIANPRRERILTPYYFPGPLQEISGTSTTWKTHPNVTMATLAIPSWAATAKVVFSATNIRLAEGAIFAGFRFMLGSTEAVQEVRIDDNQGTSARRVYVEIVETIDLTTTAGAAMRGTNQPFRARMRTDAFNDGKIGADSLTSYKIDVEFLEGRL
>NZ_LN831788|5147:14597|12274_12964_+|WP_079164025.1|DBSCAN-SWA
MSGTGAQIRAEERRWRRGDIFTVAIAVFLGLAMAWIVLSVQQLRSDLKVSNEARDALARQVLELGEKPVTSESQGRSDPSKPVPGPKGDPGSPGPSGPAGRAGATGPSGRPGADGRNGVSTTGLPGPPGQDGAPGQPGTNGQPGADGQPGPPGPQGEPGPQGEPGPEGPQGPPGQDGKDGQTCPDGYSLQAPADDPDALVCRRDGAPQPEPQPSPQPTVLGVAPERRRA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_047121225.1|5147_6098_+	hypothetical protein	A0A249XNP0	Brevibacterium_phage	2.1e-13	36.5
WP_047121226.1|6094_7195_+	hypothetical protein	A0A1B3B1I0	Gordonia_phage	1.0e-16	23.9
WP_053042656.1|7194_9579_+	hypothetical protein	A0A249XNP1	Brevibacterium_phage	2.8e-14	33.3
WP_047121227.1|9575_9917_+	hypothetical protein	NA	NA	NA	NA
WP_053042657.1|10071_10458_+	hypothetical protein	K4IBM9	Streptomyces_virus	1.8e-11	43.9
WP_047121228.1|10457_11396_+	N-acetylmuramoyl-L-alanine amidase	A0A1J0MCN5	Streptomyces_phage	1.5e-109	63.5
WP_047121229.1|11392_11581_+	hypothetical protein	W8ED25	Mycobacterium_phage	9.1e-06	48.0
WP_047121230.1|11577_11961_+	hypothetical protein	NA	NA	NA	NA
WP_047121231.1|11984_12275_+	hypothetical protein	NA	NA	NA	NA
WP_079164025.1|12274_12964_+	collagen-like protein	NA	NA	NA	NA
WP_047121232.1|12985_13723_-	FAD-dependent thymidylate synthase	A0A2H5BLS9	Streptomyces_phage	6.2e-82	65.0
WP_047121233.1|14015_14597_+	dCTP deaminase	I4AZP2	Saccharomonospora_phage	1.6e-72	70.5