CRISPRimmunity

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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_LS483523	Streptococcus pneumoniae strain 4041STDY6836169 chromosome 1	4 crisprs	cas3,RT,DEDDh,DinG	0	29	13	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_LS483523_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_LS483523_1

405911-406006

Orphan

Consensus_repeat	Method
TTATATATAAAAATTTTACACATT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_LS483523_1

>merge|NZ_LS483523|1|405911-406006|CRISPRCasFinder
TTATATATAAAAATTTTACACATTTCTCTTGACAGGGCTTTCTTTTAGATGTACAATGTATGTGTAGAAAAATTATATATAAAAATCTTACACATT

>NZ_LS483523|1|1|405911-406006|CRISPRCasFinder
TTATATATAAAAATTTTACACATT	TCTCTTGACAGGGCTTTCTTTTAGATGTACAATGTATGTGTAGAAAAA
TTATATATAAAAATCTTACACATT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LS483523.1\|WP_000148249.1\|415450_415801_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_001030031.1\|410274_411261_-\|rhodanese-related-sulfurtransferase	unknown	unknown	gnl\|CDD\|234663
NZ_LS483523.1\|WP_001035700.1\|401611_403462_-\|polysaccharide-biosynthesis-protein	unknown	unknown	gnl\|CDD\|224011
NZ_LS483523.1\|WP_000800407.1\|411532_413008_-\|DUF3502-domain-containing-protein	unknown	unknown	gnl\|CDD\|378792
NZ_LS483523.1\|WP_000092756.1\|416567_417179_-\|30S-ribosomal-protein-S4	unknown	unknown	gnl\|CDD\|235411
NZ_LS483523.1\|WP_111683434.1\|406922_407834_+\|DUF4097-domain-containing-protein	unknown	unknown	gnl\|CDD\|372574
NZ_LS483523.1\|WP_000273864.1\|406023_406350_+\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_LS483523.1\|WP_001189285.1\|397781_398102_+\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_016398064.1\|398153_398726_-\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|212030
NZ_LS483523.1\|WP_023396101.1\|414202_415132_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_LS483523.1\|WP_000200892.1\|400541_401174_+\|HAD-family-hydrolase	unknown	unknown	gnl\|CDD\|319798
NZ_LS483523.1\|WP_000723959.1\|394917_397026_-\|bacteriocin-associated-integral-membrane-family-protein	unknown	unknown	gnl\|CDD\|273736
NZ_LS483523.1\|WP_073077611.1\|397080_397374_-\|lactococcin-972-family-bacteriocin	unknown	unknown	gnl\|CDD\|370615
NZ_LS483523.1\|WP_000808464.1\|407896_408961_+\|membrane-protein	unknown	unknown	gnl\|CDD\|370966
NZ_LS483523.1\|WP_001075102.1\|413265_414189_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_LS483523.1\|WP_000198687.1\|406336_406930_+\|DUF1700-domain-containing-protein	unknown	unknown	gnl\|CDD\|227053
NZ_LS483523.1\|WP_000500040.1\|399647_400520_+\|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-alpha	unknown	unknown	gnl\|CDD\|129801
NZ_LS483523.1\|WP_000838912.1\|398967_399639_+\|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta	unknown	unknown	gnl\|CDD\|224674
NZ_LS483523.1\|WP_023396549.1\|403503_404661_-\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133016
NZ_LS483523.1\|WP_000744908.1\|404718_405885_+\|CynX/NimT-family-MFS-transporter	unknown	unknown	gnl\|CDD\|225365

Protein	Function_ID	Function_description	E-value
NZ_LS483523.1\|WP_001030031.1\|410274_411261_-\|rhodanese-related-sulfurtransferase	gnl\|CDD\|234663	PRK00142, PRK00142, rhodanese-related sulfurtransferase.	0
NZ_LS483523.1\|WP_000800407.1\|411532_413008_-\|DUF3502-domain-containing-protein	gnl\|CDD\|378792	pfam12010, DUF3502, Domain of unknown function (DUF3502). This presumed domain is functionally uncharacterized. This domain is found in bacteria. This domain is about 140 amino acids in length. This domain is found associated with pfam01547.	4.24398e-44
NZ_LS483523.1\|WP_000092756.1\|416567_417179_-\|30S-ribosomal-protein-S4	gnl\|CDD\|235411	PRK05327, rpsD, 30S ribosomal protein S4; Validated.	1.01065e-118
NZ_LS483523.1\|WP_111683434.1\|406922_407834_+\|DUF4097-domain-containing-protein	gnl\|CDD\|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	4.74959e-40
NZ_LS483523.1\|WP_000273864.1\|406023_406350_+\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	3.12912e-19
NZ_LS483523.1\|WP_001035700.1\|401611_403462_-\|polysaccharide-biosynthesis-protein	gnl\|CDD\|224011	COG1086, COG1086, Predicted nucleoside-diphosphate sugar epimerases [Cell envelope biogenesis, outer membrane / Carbohydrate transport and metabolism].	0
NZ_LS483523.1\|WP_016398064.1\|398153_398726_-\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|212030	cd00118, LysM, Lysin Motif is a small domain involved in binding peptidoglycan. LysM, a small globular domain with approximately 40 amino acids, is a widespread protein module involved in binding peptidoglycan in bacteria and chitin in eukaryotes. The domain was originally identified in enzymes that degrade bacterial cell walls, but proteins involved in many other biological functions also contain this domain. It has been reported that the LysM domain functions as a signal for specific plant-bacteria recognition in bacterial pathogenesis. Many of these enzymes are modular and are composed of catalytic units linked to one or several repeats of LysM domains. LysM domains are found in bacteria and eukaryotes.	1.19314e-14
NZ_LS483523.1\|WP_023396101.1\|414202_415132_-\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	8.06751e-143
NZ_LS483523.1\|WP_000200892.1\|400541_401174_+\|HAD-family-hydrolase	gnl\|CDD\|319798	cd04302, HAD_5NT, haloacid dehalogenase (HAD)-like 5'-nucleotidases similar to the Pseudomonas aeruginosa PA0065. 5'-nucleotidases dephosphorylate nucleoside 5'-monophosphates to nucleosides and inorganic phosphate. Purified Pseudomonas aeruginosa PA0065 displayed high activity toward 5'-UMP and 5'-IMP, significant activity against 5'-XMP and 5'-TMP, and low activity against 5'-CMP. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	4.4095e-97
NZ_LS483523.1\|WP_000723959.1\|394917_397026_-\|bacteriocin-associated-integral-membrane-family-protein	gnl\|CDD\|273736	TIGR01654, unnamed_protein_product, bacteriocin-associated integral membrane (putative immunity) protein. This model represents a family of integral membrane proteins, most of which are about 650 residues in size and predicted to span the membrane seven times. Nearly half of the members of this family are found in association with a member of the lactococcin 972 family of bacteriocins (TIGR01653). Others may be associated with uncharacterized proteins that may also act as bacteriocins. Although this protein is suggested to be an immunity protein, and the bacteriocin is suggested to be exported by a Sec-dependent process, the role of this protein is unclear. [Cellular processes, Toxin production and resistance].	0
NZ_LS483523.1\|WP_073077611.1\|397080_397374_-\|lactococcin-972-family-bacteriocin	gnl\|CDD\|370615	pfam09683, Lactococcin_972, Bacteriocin (Lactococcin_972). These sequences represent bacteriocins related to lactococcin. Members tend to be found in association with a seven transmembrane putative immunity protein.	4.60159e-22
NZ_LS483523.1\|WP_000808464.1\|407896_408961_+\|membrane-protein	gnl\|CDD\|370966	pfam10310, DUF5427, Family of unknown function (DUF5427). This is a domain of unknown function. Family members found in Saccharomyces cerevisiae, are synthetic lethal with genes involved in maintenance of telomere capping. However, experimental evidence is yet to verify the exact function of family members and the domain.	0.000226352
NZ_LS483523.1\|WP_001075102.1\|413265_414189_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.04007e-69
NZ_LS483523.1\|WP_000198687.1\|406336_406930_+\|DUF1700-domain-containing-protein	gnl\|CDD\|227053	COG4709, COG4709, Predicted membrane protein [Function unknown].	2.84602e-63
NZ_LS483523.1\|WP_000500040.1\|399647_400520_+\|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-alpha	gnl\|CDD\|129801	TIGR00718, Probable_L-serine_dehydratase_alpha_chain, L-serine dehydratase, iron-sulfur-dependent, alpha subunit. This enzyme is also called serine deaminase. L-serine dehydratase converts serine into pyruvate in the gluconeogenesis pathway from serine. This model describes the alpha chain of an iron-sulfur-dependent L-serine dehydratase, found in Bacillus subtilis. A fairly deep split in a UPGMA tree separates members of this family of alpha chains from the homologous region of single chain forms such as found in Escherichia coli. This family of enzymes is not homologous to the pyridoxal phosphate-dependent threonine deaminases and eukaryotic serine deaminases. [Energy metabolism, Amino acids and amines, Energy metabolism, Glycolysis/gluconeogenesis].	1.44295e-105
NZ_LS483523.1\|WP_000838912.1\|398967_399639_+\|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta	gnl\|CDD\|224674	COG1760, SdaA, L-serine deaminase [Amino acid transport and metabolism].	1.1908e-89
NZ_LS483523.1\|WP_023396549.1\|403503_404661_-\|glycosyltransferase-family-2-protein	gnl\|CDD\|133016	cd02525, Succinoglycan_BP_ExoA, ExoA is involved in the biosynthesis of succinoglycan. Succinoglycan Biosynthesis Protein ExoA catalyzes the formation of a beta-1,3 linkage of the second sugar (glucose) of the succinoglycan with the galactose on the lipid carrie. Succinoglycan is an acidic exopolysaccharide that is important for invasion of the nodules. Succinoglycan is a high-molecular-weight polymer composed of repeating octasaccharide units. These units are synthesized on membrane-bound isoprenoid lipid carriers, beginning with galactose followed by seven glucose molecules, and modified by the addition of acetate, succinate, and pyruvate. ExoA is a membrane protein with a transmembrance domain at c-terminus.	1.1206e-108
NZ_LS483523.1\|WP_000744908.1\|404718_405885_+\|CynX/NimT-family-MFS-transporter	gnl\|CDD\|225365	COG2807, CynX, Cyanate permease [Inorganic ion transport and metabolism].	1.76726e-125

>NZ_LS483523.1|WP_000744908.1|404718_405885_+|CynX/NimT-family-MFS-transporter
MKKQSLFFVPGIILIGVSLRTPFTVLPIILGNISQGLEVEVSSLGVLTSLPLLMFTLFSPFSTRLAQKIGLEHLFTYSLFFLTIGSLIRLINLPLLYLGTLMVGASVAVINVLLPSLIQANQPKKIGFLTTLYVTSMGIATALASYLAVPITQASSWKGLILLLTLLCLATFLVWLPNHRYNHRLAPQTKQKSQIKVMRNKQVWAIIIFSGFQSLIFYTVMTWLPTMSIHAGLSSHEAGLLTSILSLISIPFSMTIPSLTTSLSTRNRQLMLTLVSLAGVVGISMLFFPINNFIYWLTIHLLIGTATSALFPYLMVNFSLKTSAPEKTAQLSGLSQTGGYILAAFGPTLFGYSFDLFHSWVPAVAALLLIYILMTVALFTVDRADKIL
>NZ_LS483523.1|WP_023396549.1|403503_404661_-|glycosyltransferase-family-2-protein
MSSKVSGFQDKNGKVLKIMIEWWKEKFRRVVVTQNVESLLVSIVISAYNEEKYLPGLIEDLKNQTYPKENVEILFINAMSTDGTTAIIQQFIKEDTEFNSIRLYNNPKKNQASGFNLGVKHSVGDLILKIDAHSKVTESFVMNNVAIIQQGEFVCGGPRPTIVEGKGKWAETLHLVEENMFGSSIANYRNSSEDRYVSSIFHGMYKREVFQKVGLVNEQLGRTEDNDIHYRIREHGYKIRYSPSILSYQYIRPTFKKMLHQKYSNGLWIGLTSHVQFKCLSLFHYVPCLFVLSLVFSLALLPITFVFITLLLGAYFLLLSLLTLLTLLKHKNGFLIVMPFLLFSIHFAYGFGTIVGLIRGFKWKKEYKRTIIYLDKISQINKNML
>NZ_LS483523.1|WP_001035700.1|401611_403462_-|polysaccharide-biosynthesis-protein
MNKKLTDYVIDLVEILNKQQKQVFWGIFDIFSMVVSIIVSYILFYGLINPAPVDYIIYTSLAFLFYQLMIGFWGLNASISRYSKITDFMKIFFGVTASSVLSYSICYAFLPLFSIRFIILFILLSTFLILLPRITWQLIYSRRKKGSGDGEHRRTFLIGAGDGGALFMDSYQHPTSELELVGILDKDSKKKGQKLGGIPVLGSYDNLPELAKRHQIERVIVAIPSLDPSEYERILQMCNKLGVKCYKMPKVETVVQGLHQAGTGFQKIDITDLLGRQEIRLDESRLGAELTGKTILVTGAGGSIGSEICRQVSRFNPERIVLLGHGENSIYLVYHELIRKFQGIDYVPVIADIQDYDRLLQVFEQYKPAIVYHAAAHKHVPMMERNPKEAFKNNIRGTYNVAKAVDEAKVSKMVMISTDKAVNPPNVMGATKRVAELIVTGFNQRSQSTYCAVRFGNVLGSRGSVIPVFERQIAEGGPVTVTDFRMTRYFMTIPEASRLVIHAGAYAKDGEVFILDMGKPVKIYDLAKKMVLLSGHTESEIPIVEVGIRPGEKLYEELLVSTELVDNQVMDKIFVGKVNVMPLESINQKIGEFRTLSGDELKQAIIAFANQTTHIE
>NZ_LS483523.1|WP_000200892.1|400541_401174_+|HAD-family-hydrolase
MTSITAIFFDLDGTLVDSSIGIHNAFTYTFKELGVPSPDAKTIRGFMGPPLESSFATCLSKDQISEAVQIYRSYYKAKGIYEAQLFPQIIDLLEELSSSYPLYITTTKDTSTAQDMAKNLEIHHFFDGIYGSSPEAPHKADVIHQALQTHQLAPEQAIIIGDTKFDMLGARETGIQKLAITWGFGEQADLLNYQPDYIAHKPLEVLAYFQ
>NZ_LS483523.1|WP_000500040.1|399647_400520_+|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-alpha
MFYSIKELVEQADLDFQGNVAELMITTEFELTGREREEVFLLMERNLEVMKASVQLGLNENKSRSGLTGGDAAKLDHYIKNEKTLSDYTILSAARNAIAVNEHNAKMGLVCATPTAGSAGCLPSVLTAAIEKLDLSHEQQLDFLFAAGAFGLVIANNASISGAEGGCQAEVGSASAMSAAALTLAAGGTPYQASQAIAFVIKNMLGLICDPVAGLVEVPCVKRNAMGASFAFIAADMALAGIESKIPVDEVIDAMYQVGASMPTAFRETAEGGLATTPTGRRLQKEIFGE
>NZ_LS483523.1|WP_000838912.1|398967_399639_+|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta
MKSLRFQSVFDIIGPVMIGPSSSHTAGAVRIGKIVSSIFDDTPTEVEFQLFNSFAKTYRGHGTDLALVAGILGMDTDDPEIPNSLEIAHKRGIKIVWTIQKDSNAPHPNTTKITVKNAHKTISVTGISIGGGNIQVTELNGFAVSLNMNTPTIIIVHQDIPGMIALVTEALSRYGINIAQMNVTREKAGEKAIMIIEVDSRNCDEAIEEIRKIPHLHNVNFFK
>NZ_LS483523.1|WP_016398064.1|398153_398726_-|LysM-peptidoglycan-binding-domain-containing-protein
MKSITKKIKATLAGVAALFAVFAPSFVSAQESSTYTVKEGDTLSEIAETHNTTVEKLAENNHIDNIHLIYVGQELVIDGPVAPVATPAPATYAAPAAQDETVSAPVVSETVVSTVSGSEAEAKEWIAQKESGGSYTATNGRYIGRYQLTDSYLNGDYSAENQERVADAYVAGRYGSWTAAKNFWLNNGWY
>NZ_LS483523.1|WP_001189285.1|397781_398102_+|hypothetical-protein
MQRLEVYKNYQHLYDLRIAILLNLSTLYLYNQDKNMCKQICYTLLEDAKNKKSYDRLVICYVRIGICTDDSKLIQKGFSLLELTEETSMLSHLKKEVEIYYQAKER
>NZ_LS483523.1|WP_073077611.1|397080_397374_-|lactococcin-972-family-bacteriocin
MIGEINHEKIGVASLMVCSILASTSVLAVWVDGGQWNYGVGWSGNFGYSDYLHSTRSHTATVKDGNKFSKDRAEAEAWARASIFKFPPTGMEYFYGF
>NZ_LS483523.1|WP_000723959.1|394917_397026_-|bacteriocin-associated-integral-membrane-family-protein
MKKISHLCMLLLLLCTTFFVFNVNYTREVVRIQEMGKTVDSLDLYLKDINEPAASVLRFFEDVSKEYKVSIIKTDSGDEVVKSGVFDKDTFPYQEFGISSLDFTTDGEGVYSNKEISNKLGTIPTFLKAKPIQLMTFQTYIKDTSRSLNGRYTITSTQEMDKDRIVQKWSDFFKIDQATLLEPTYKSAVEVINRDLLLSAIVFVLAILLLVLVTVYQPMMEMKRVGVQKLLGFQDRAVLADVVKGNLYLLLGGALVINLGVFFLLDYKPKDLFPMLWLSHFLLLQLYLFISWLTYLLIQKMTISSLLKGFSSFKFGLIFNYVMKIGTTILLTALLIGVGRSLEQENKELAYQQQWVSQGNYLTLETFKLNDNLWQEELAGSGKSTDYFYRFYQDLVEKTQAGYVQSSSLPVKNFVQSEQIQQYQLTDTVDVYYANRNFLKSKGFKLPDTGIKKVILMPASTKGEEDKNQLLGKLIAFHSMKYEEQQKRTIEEMDVEIAYYEGDWSFFPYSDKRKENLSNPIISLVNDSDMMWDEKASLSTTGLNNPIKIENTVQHQKEITELVEKLSDGNYLKFSSIQAIQQEKVDSYRDAVRNFNLLFALFGLLSMMISYFLLVTTFLLKRRDIITKKFMGWKLVDRYRPLLVLLLLGYSFPLLVLIFFAHAFLPLLLFAGFTCLDILFVLGLASRMEKRSLVELLKGGIL
>NZ_LS483523.1|WP_000273864.1|406023_406350_+|PadR-family-transcriptional-regulator
MYFPTSSALIEFLILAVLEQGDSYGYEISQTIKLIANIKESTLYPILKKLEGNSFLTTYSREFQGRMRKYYSLTNGGIEQLLTLKDEWTLYTDTINGIIEGSIRHDKN
>NZ_LS483523.1|WP_000198687.1|406336_406930_+|DUF1700-domain-containing-protein
MTRTEYLTQLELYLKKLPEADRIEAMDYFRELFDDAGVEGEEELIASLGTPKEAAHEVLSNLLDKKINEAPAQKNNRQILHIALLALLAAPIGIPLGIAILVTLFAILVAALTVILAFFAVSILGIIGGFLFLVESFTILAQAKSAFILIFGSGLLAIGASSLVLLGISYVARFFGLLIVRLVQFVLKKGKRGNQHA
>NZ_LS483523.1|WP_111683434.1|406922_407834_+|DUF4097-domain-containing-protein
MRKWTKGFLIFGMVTTVIGFILLFVGIQSDGIKSLLSMSKEPVYDSRTEKLTFGKEVENLEITLHQHTLTITDSFDDQIHISYHPSLSAHHDLITNQNDRTLSLTDKKLSETPFLSSGIGGILHIASSYSSRFEEVILRLPKGRTLKGINISANRGQTTIINASLENATLNTNSYILRIEGSRIKNSKLTTPNIVNIFDTVLTDSQLESTDNHFHAENIQVHGKVELTAKDYLRIILDQKESQRINWDISSNYGSIFQFTREKPESRGTELSNPYKTEKTDVKDQLIARSDDNIDLISTPSRR
>NZ_LS483523.1|WP_000808464.1|407896_408961_+|membrane-protein
MKQEWFESNDFVKTTSKNKPEEQAQEVADKAEETIANLDTPIGKNTQVEEEVSQAEVELESQQEEKIETPEGGEARTEIEEKKASNSTEEEPDLSKETEKVTIAEESQEALPQQKATTKEPLLISKSLKSPYIPDQAPKSRDKWKEQVLDFWSWLVEAIKSPTSKLETSITHSYTAFLLLILFSASSFFFSIYHIKHAYYGHIASINSRFPEQLAPLTLFSIISILVATTLFFFSFLLGSFVVRRFIHQEKDWTLDKVLQQYSQLLAIPIFLTAIASFFAFFDSLRFTALLCVISIGIILLASLHIITRPSQASETDSFYQLFLSVLVNGVIILLFFVAEVALIGDYLRILAFL
>NZ_LS483523.1|WP_001030031.1|410274_411261_-|rhodanese-related-sulfurtransferase
MAKDIRVLLYYLYTPIENAEQFAADHLAFCKSIGLKGRILVADEGINGTVSGDYETTQKYMDYVHSLPGMEELWFKIDEENEQAFKKMFVRYKKEIVHLGLEDNDFDNDINPLETTGAYLSPKEFKEALLDKDTVVLDTRNDYEYDLGHFRGAIRPDIRNFRELPQWVRDNKEKFMDKRVVVYCTGGVRCEKFSGWMVREGYKDVGQLHGGIATYGKDPEVQGELWDGKMYVFDERIAVDVNHVNPTIVGKDWFDGTPCERYVNCGNPFCNRRILTSEENEDKYLRGCSHECRVHPRNRYVSKNELTQAEVIERLAAIGESLDQAATV
>NZ_LS483523.1|WP_000800407.1|411532_413008_-|DUF3502-domain-containing-protein
MKNWKKYAFASASVVALAAGLAACGNLTGNSKKAADSGDKPVIKMYQIGDKPDNLDELLANANKIIEEKVGAKLDIQYLGWGDYGKKMSVITSSGENYDIAFADNYIVNAQKGAYADLTELYKKEGKDLYKALDPAYIKGNTVNGKIYAVPVAANVASSQNFAFNGTLLAKYGIDISGVTSYETLEPVLKQIKEKAPDVVPFAIGKVFIPSDNFDYPVANGLPFVIDLEGDTTKVVNRYEVPRFKEHLKTLHKFYEAGYIPKDVATSDTSFDLQQDTWFVREETVGPADYGNSLLSRVANKDIQIKPITNFIKKNQTTQVANFVISNNSKNKEKSMEILNLLNTNPELLNGLVYGPEGKNWEKIEGKENRVRVLDGYKGNTHMGGWNTGNNWILYINENVTDQQIENSKKELAEAKESPALGFIFNTDNVKSEISAIANTMQQFDTAINTGTVDPDKAIPELMEKLKSEGAYEKVLNEMQKQYDEFLKNKK
>NZ_LS483523.1|WP_001075102.1|413265_414189_-|carbohydrate-ABC-transporter-permease
MAKKKIKKEKIDNVGIHSFSKKADIFFSIISGLIALSCILPFVFVIIISVTDEKSLLQYGYSFFPSQFGLDGFEFLAQFKDKILQALFISVFVTVVGTLTNVFITTTYAYAISRTTFKYRRFFTIFVLLSMLFNAGLVPGYIMVTRVLQLGDTVWALIVPMLLSPFNIILMRSFFKKTIPEAILESARIDGASEARIFFQICLPLSLPGIATITLLTALGFWNDWFNALLYIKSDNLYPLQYLLMQIQQNMDYIAKAVGLTGQLGVALPKETGRMAMVVVATLPIAILYPFFQRYFVKGLTIGGVKE
>NZ_LS483523.1|WP_023396101.1|414202_415132_-|sugar-ABC-transporter-permease
MKKFSKTLRDNWIFLLMVLPGALWLILFFYIPVFGNVVAFKDYHMTSNGFIDSIINSKWVGLDNFRFLFSSRDAFIITRNTVLYNLGFIFLGLVVSVGIAIILSELRSKRMVKIFQTSMLFPYFLSWVIISFFTDAFLNIDKGVFNHLLESLGLKEVNFYADLGIWPYLLLFLGIWKGFGYSSVMYYATIMGIDPTYYEAATVDGASKWQRIRNVTIPQLTPLVTVLTILAVGNIFRADFGLFYQIPHNAGQLYNVTNVLDVYVFNGLTQTADIGMAAAAGLYQSVVGLILVILSNLFARRVDPNSALF
>NZ_LS483523.1|WP_000148249.1|415450_415801_-|hypothetical-protein
MTGVSNPTTDSAPLVLAEAKKAFADDSLTEQGLRDILQTVKDAIASLESIKESQSATKDGGQTAGKETADKDVLENSQEELQKAVLFLADEKGSEHTAAELIDNLKEVIAKLKANA
>NZ_LS483523.1|WP_000092756.1|416567_417179_-|30S-ribosomal-protein-S4
MSRYTGPSWKQARRLGLSLTGTGKELARRNYVPGQHGPNNRSKLSEYGLQLAEKQKLRFTYGVGEKQFRNLFVQATKIKGGILGFNFMLLLERRLDNVVYRLGLATTRRQARQFVNHGHILVDGKRVDIPSYRVTPGQVISVREKSLKVPAILEAVEATLGRPAFVSFDAEKLEGSLTRLPERDEINPEINEALVVEFYNKML

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Crispr_ID: NZ_LS483523_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_LS483523_2

949239-949323

Orphan

Consensus_repeat	Method
AACAAAAATGAAACGTTTCAAAAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_LS483523_2

>merge|NZ_LS483523|2|949239-949323|CRISPRCasFinder
AACAAAAATGAAACGTTTCAAAAAAGAAATAAAGAGACAGCGCCAAGCGCTATCTTTTCTAGAAAAAAATGAAACGTTTCAAAAA

>NZ_LS483523|2|2|949239-949323|CRISPRCasFinder
AACAAAAATGAAACGTTTCAAAAA	AGAAATAAAGAGACAGCGCCAAGCGCTATCTTTTCTA
GAAAAAAATGAAACGTTTCAAAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LS483523.1\|WP_000229331.1\|942118_942889_+\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|376667
NZ_LS483523.1\|WP_000064115.1\|944255_944864_-\|Asp23/Gls24-family-envelope-stress-response-protein	unknown	unknown	gnl\|CDD\|224221
NZ_LS483523.1\|WP_023396411.1\|957890_958361_+\|DUF3013-family-protein	unknown	unknown	gnl\|CDD\|337951
NZ_LS483523.1\|WP_023396412.1\|957147_957600_+\|type-II-toxin-antitoxin-system-HicB-family-antitoxin	unknown	unknown	gnl\|CDD\|224514
NZ_LS483523.1\|WP_054365899.1\|954670_955942_-\|replication-associated-recombination-protein-A	unknown	unknown	gnl\|CDD\|237355
NZ_LS483523.1\|WP_054365898.1\|952806_954126_+\|glycoside-hydrolase-family-32-protein	unknown	unknown	gnl\|CDD\|224536
NZ_LS483523.1\|WP_001084979.1\|949333_950251_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_LS483523.1\|WP_000109957.1\|944021_944225_-\|CsbD-family-protein	unknown	unknown	gnl\|CDD\|225777
NZ_LS483523.1\|WP_000455066.1\|944902_945073_-\|DUF2273-domain-containing-protein	unknown	unknown	gnl\|CDD\|227834
NZ_LS483523.1\|WP_001820780.1\|945734_945899_-\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl\|CDD\|225170
NZ_LS483523.1\|WP_000030213.1\|945084_945651_-\|alkaline-shock-response-membrane-anchor-protein-AmaP	unknown	unknown	gnl\|CDD\|380217
NZ_LS483523.1\|WP_023396415.1\|951180_952797_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270299
NZ_LS483523.1\|WP_001048906.1\|956615_956795_+\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_001865109.1\|943149_943437_-\|IS30-family-transposase	unknown	unknown	gnl\|CDD\|225382
NZ_LS483523.1\|WP_000782429.1\|941255_942104_+\|formylglycine-generating-enzyme-family-protein	unknown	unknown	gnl\|CDD\|335469
NZ_LS483523.1\|WP_023396416.1\|948182_949184_+\|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_LS483523.1\|WP_023396413.1\|956931_957111_+\|type-II-toxin-antitoxin-system-HicA-family-toxin	unknown	unknown	gnl\|CDD\|377942
NZ_LS483523.1\|WP_000797961.1\|950261_951152_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_LS483523.1\|WP_001205283.1\|946340_947822_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|285470
NZ_LS483523.1\|WP_000818078.1\|956211_956451_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_LS483523.1\|WP_000229331.1\|942118_942889_+\|sulfite-exporter-TauE/SafE-family-protein	gnl\|CDD\|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	1.65578e-17
NZ_LS483523.1\|WP_000064115.1\|944255_944864_-\|Asp23/Gls24-family-envelope-stress-response-protein	gnl\|CDD\|224221	COG1302, COG1302, Uncharacterized protein conserved in bacteria [Function unknown].	1.35166e-33
NZ_LS483523.1\|WP_023396411.1\|957890_958361_+\|DUF3013-family-protein	gnl\|CDD\|337951	pfam11217, DUF3013, Protein of unknown function (DUF3013). This bacterial family of proteins with unknown function appear to be restricted to Firmicutes.	1.71703e-64
NZ_LS483523.1\|WP_023396412.1\|957147_957600_+\|type-II-toxin-antitoxin-system-HicB-family-antitoxin	gnl\|CDD\|224514	COG1598, COG1598, Predicted nuclease of the RNAse H fold, HicB family [General function prediction only].	1.98944e-11
NZ_LS483523.1\|WP_054365899.1\|954670_955942_-\|replication-associated-recombination-protein-A	gnl\|CDD\|237355	PRK13342, PRK13342, recombination factor protein RarA; Reviewed.	0
NZ_LS483523.1\|WP_054365898.1\|952806_954126_+\|glycoside-hydrolase-family-32-protein	gnl\|CDD\|224536	COG1621, SacC, Beta-fructosidases (levanase/invertase) [Carbohydrate transport and metabolism].	1.1619e-177
NZ_LS483523.1\|WP_001084979.1\|949333_950251_+\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.73729e-138
NZ_LS483523.1\|WP_000109957.1\|944021_944225_-\|CsbD-family-protein	gnl\|CDD\|225777	COG3237, COG3237, Uncharacterized protein conserved in bacteria [Function unknown].	1.20386e-07
NZ_LS483523.1\|WP_000455066.1\|944902_945073_-\|DUF2273-domain-containing-protein	gnl\|CDD\|227834	COG5547, COG5547, Small integral membrane protein [Function unknown].	9.45975e-16
NZ_LS483523.1\|WP_001820780.1\|945734_945899_-\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl\|CDD\|225170	COG2261, COG2261, Predicted membrane protein [Function unknown].	1.78115e-05
NZ_LS483523.1\|WP_000030213.1\|945084_945651_-\|alkaline-shock-response-membrane-anchor-protein-AmaP	gnl\|CDD\|380217	NF033218, anchor_AmaP, alkaline shock response membrane anchor protein AmaP. The founding member of this family, AmaP (Asp23 membrane anchoring protein), is related to Asp23 through part of its length, but includes a highly hydrophobic N-terminal region that should make it an integral membrane protein. Asp23 (alkaline shock protein of 23 kDa), described in PMID:7864904, is a cytosolic protein in Staphylococcus aureus, strongly induced by a pH shift from 7 to 10, and also recruited to the membrane. AmaP appears to be the partner protein with an integral membrane segment and the ability to anchor Asp23 to the membrane. This model was built to identify full-length homologs of AmaP, while excluding Asp23. Some but not all members of this family score above the cutoffs of Pfam model version PF03780.11, but full-length homologs of Asp23 score considerably higher. Asp23 family members previously were known as DUF322.	7.65552e-46
NZ_LS483523.1\|WP_023396415.1\|951180_952797_+\|extracellular-solute-binding-protein	gnl\|CDD\|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is 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. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	0
NZ_LS483523.1\|WP_001865109.1\|943149_943437_-\|IS30-family-transposase	gnl\|CDD\|225382	COG2826, Tra8, Transposase and inactivated derivatives, IS30 family [DNA replication, recombination, and repair].	4.62746e-14
NZ_LS483523.1\|WP_000782429.1\|941255_942104_+\|formylglycine-generating-enzyme-family-protein	gnl\|CDD\|335469	pfam03781, FGE-sulfatase, Sulfatase-modifying factor enzyme 1. This domain is found in eukaryotic proteins required for post-translational sulfatase modification (SUMF1). These proteins are associated with the rare disorder multiple sulfatase deficiency (MSD). The protein product of the SUMF1 gene is FGE, formylglycine (FGly),-generating enzyme, which is a sulfatase. Sulfatases are enzymes essential for degradation and remodelling of sulfate esters, and formylglycine (FGly), the key catalytic in the active site, is unique to sulfatases. FGE is localized to the endoplasmic reticulum (ER) and interacts with and modifies the unfolded form of newly synthesized sulfatases. FGE is a single-domain monomer with a surprising paucity of secondary structure that adopts a unique fold which is stabilized by two Ca2+ ions. The effect of all mutations found in MSD patients is explained by the FGE structure, providing a molecular basis for MSD. A redox-active disulfide bond is present in the active site of FGE. An oxidized cysteine residue, possibly cysteine sulfenic acid, has been detected that may allow formulation of a structure-based mechanism for FGly formation from cysteine residues in all sulfatases. In Mycobacteria and Treponema denticola this enzyme functions as an iron(II)-dependent oxidoreductase.	3.26408e-66
NZ_LS483523.1\|WP_023396416.1\|948182_949184_+\|LacI-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	4.06031e-98
NZ_LS483523.1\|WP_023396413.1\|956931_957111_+\|type-II-toxin-antitoxin-system-HicA-family-toxin	gnl\|CDD\|377942	pfam07927, HicA_toxin, HicA toxin of bacterial toxin-antitoxin,. HicA_toxin is a bacterial family of toxins that act as mRNA interferases. The antitoxin that neutralizes this is family HicB, pfam15919.	1.64571e-08
NZ_LS483523.1\|WP_000797961.1\|950261_951152_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.20755e-67
NZ_LS483523.1\|WP_001205283.1\|946340_947822_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|285470	pfam08270, PRD_Mga, M protein trans-acting positive regulator (MGA) PRD domain. Mga is a DNA-binding protein that activates the expression of several important virulence genes in group A streptococcus in response to changing environmental conditions. This corresponds to the PRD like region.	7.1659e-74

>NZ_LS483523.1|WP_023396416.1|948182_949184_+|LacI-family-DNA-binding-transcriptional-regulator
MVEQRKSITMKDVALEAGVSVGTVSRVINKEKGIKEVTLKKVEQAIKTLNYIPDYYARGMKKNRTETIAIIVPSIWHPFFSEFAMHVENEVYKRNNKLLLCSINGTNREQDYLEMLRHNKVDGVVAITYSPIEHYLTSGIPFVSIDRTYSDIAIPCVSSDNDAGGREAAKQLISKGCQHLAFVGGHNTTINETKRCRISFEKYVQEHKIPLSIFDLDETVTDYYGKLESFLEENSSIDGIFTINDFTALDVIEILEKNGKRIPHDVQIIGYDGIKMAGDRDYLLSTIEQPLEEMAKEAVRILFDIIDGKTVNLQTILPVKFVEGKTTKNENKS
>NZ_LS483523.1|WP_001205283.1|946340_947822_+|helix-turn-helix-domain-containing-protein
MRDLLSKKSHRQLELLELLFEHKRWFHRSELAELLNCTERAVKDDLSHVKSAFPDLIFHSSTNGIRIINTDDSDIEMVYHHFFKHSTHFSILEFIFFNEGCQAESICKEFYISSSSLYRIISQINKVIKRQFQFEVSLTPVQIIGNERDIRYFFAQYFSEKYYFLEWPFENFSSEPLSQLLELVYKETSFPMNLSTHRMLKLLLVTNLYRIKFGHFMEVDKDSFNDQSLDFLMQAEGIEGVAQSFESEYNISLDEEVVCQLFVSYFQKMFFIDESLFMKCVKKDSYVEKSYHLLSDFIDQISVKYQIEMENKDNLIWHLHNTAHLYRQELFTEFILFDQKGNTIRNFQNIFPKFVSDVKKELSHYLETLEVCSSSMMVNHLSYTFITHTKHLVINLLQNQPKLKVLVMSNFDQYHAKFVAETLSYYCSNNFELEVWTELELSKESLEDSSYDIIISNFIIPPIENKRLIYSNNINTVSLIYLLNAMMFIRLDE
>NZ_LS483523.1|WP_001820780.1|945734_945899_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MGIIANVFAGLVGASAGQSLLGSWGPSIAGMALLPSIVGAAIVITVVSFFTGRK
>NZ_LS483523.1|WP_000030213.1|945084_945651_-|alkaline-shock-response-membrane-anchor-protein-AmaP
MSKAKKICFIIFCILILTIFLPVLIDYHQVSDLGIHLLSWRQNSVVEFYLARYVFWGTVVLSTLVLLSILVVMFYPKRYLEIQLETKNDTLKLKNSAIEGFVRSLVSDHRLIKNPTVHVNLRKNKCFVHVEGKILPSDNIADRCQIIQNEITNGLKQFFGIERQVKLEVAVKNYQPKPQNKKTVSRVK
>NZ_LS483523.1|WP_000455066.1|944902_945073_-|DUF2273-domain-containing-protein
MEWLKQYRYPIIAGLIGVFLACLIVSFGFFKTIFVLILGALGVAAGLYIEKNYIDK
>NZ_LS483523.1|WP_000064115.1|944255_944864_-|Asp23/Gls24-family-envelope-stress-response-protein
MSNEKNTNTNVEKKDATVVAHEIKGELTYEDKVIQKIIGLSLENVSGLLGIDGGFFSNLKEKIVNSDDVTSGVNVEVGKTQVAVDLNVIVEYQKNVPALYSEIREIVSSEVAKMTDLEIVEINVNVVDIKTKEQHEADSVSLQDRVSDVAESTGEFTSEQFEKAKSGLGSGFSTVQEKVSEGVEAVKGAANGVVSHENTRVN
>NZ_LS483523.1|WP_000109957.1|944021_944225_-|CsbD-family-protein
MSVEEKLNQAKGSIKEGVGKAIGDEKMEKEGAAEKVVSKVKEVAEDAKDAVEGAVEGVKNMLSGDDK
>NZ_LS483523.1|WP_001865109.1|943149_943437_-|IS30-family-transposase
MIVSLKTKSRKAKDMAESIQGWLAQFLVNLFKSITFDCGKEFSKWKDISNHHDSESFFANLGCSRQRCLNEHSNRLLRCHDLPKQTDFNEVSQEF
>NZ_LS483523.1|WP_000229331.1|942118_942889_+|sulfite-exporter-TauE/SafE-family-protein
MVEIIYFLIIIIASGLGSISGMGGGIIIKPLMDSFGYHSVSDIAFYSSFSVFIMAIISTIKRFSQSKEIKWRLIFTVSFSSVLGGFLGHLIFQVLLSQLSVRLVSIVQMILLFVMLLVSFVLTDFKKTYQFDKIGFYMICGLLLGLISSFLGIGGGPLNVSLLMVFFSISIKEATMYSLAIIFFSQLSHLATIVVVTGLNQYHLAPVPVIFLASICGGVLGTVVSKVLPENWVRYCFKGMLFFVMEMTLYNLFHIL
>NZ_LS483523.1|WP_000782429.1|941255_942104_+|formylglycine-generating-enzyme-family-protein
MKMKKIKGGTFMMGTNSEEGFLDDFEGPQVAVSVKDFSIADTPVTNQEFAQFVKETGYKTLAERQEWSFVFILFVPEAEREGYPHPAGAPWWLQVSNACWKHPYGENSNLVGLEDHPVVHVALEDALAFCNWSGMSLPTEAQWEYAARGGRQSEYPWGDTLLEGGYYHANTWQGRFPYENTALDGFIGTAPVYEFLPNDFGLYQMIGNVWEWCRNPRYTLLASFNEDDYELPKYGIQDEEYAIRGGSFLCHCSYCNRYRVAARNGCISTSTSSHLGFRCLKE
>NZ_LS483523.1|WP_001084979.1|949333_950251_+|sugar-ABC-transporter-permease
MNSKAKQVSLWERIKKQKLLLLMTVPGLVLTFIFKYIPMYGVLIAFKDYNPLKGILGSDWIGFSEFTKFISSPNFGILLANTLKLSIYGLLLGFLPPIILAIMLNQLLSEKVKKRIQLILYAPNFISVVVIVGMIFLFFSVGGPINNFLSMFGMKADFLTNPDFFRPLYIFSGIWQGMGWASTLYTATLVNVDPALVEAARLDGANIFQRIWHIDIPALKPIMVIQFVLAAGGIMNVGYEKAFLMQTSLNLPTSEIISTYVYKVGLVSGDYSYSTAVGLFNAVINVVLLVAVNQIVKRMNNGEGI
>NZ_LS483523.1|WP_000797961.1|950261_951152_+|carbohydrate-ABC-transporter-permease
MKNSIMDTKFDRRILLLNKIIIVFIVLMTLLPLLYIVVASFMDPKVLVSRGISFNPADWTVEGYQRVFSDQSILRGFINSLLYSFGFAALTVLLSVFTAYPLSKKDLVGRRWINYFLIVTMFFGGGLVPTYLLVKELGMLNTPWAIIVPGAVNVWNIILARAYFQGLPEELVEAAVIDGANDLQIFFKIMLPLAKPIMFVLFLYAFVGQWNSYFDAMIYIKDPNLEPLQLVLRKILIQSQPGQDMIGAQAAMNEMKRLAELIKYATIVISSLPLIVMYPFFQKYFDKGIMAGSLKG
>NZ_LS483523.1|WP_023396415.1|951180_952797_+|extracellular-solute-binding-protein
MKFKTFSKSAVLLTASLAVLAACGSKNTASSPDYKLEGVTFPLQEKKTLKFMTASSPLSPKDPNEKLILQRLEKETGVHIDWTNYQSDFAEKRNLDISSGDLPDAIHNDGASDVDLMNWAKKGVIIPVEDLIDKYMPNLKKILNEKPEYKALMTAPDGHIYSFPWIEELGDGKESIHSVNDMAWINKDWLKKLGLEMPKTTDDLIKVLEAFKNGDPNGNGEADEIPFSFISGNGNEDFKFLFAAFGIGDNDDHLVVGNDGKVDFTADNDNYKEGVKFIRQLQEKGLIDKEAFEHDWNSYIAKGHDQKFGVYFTWDKNNVTGSNESYDVLPVLAGPSGQKHVARTNGMGFARDKMVITSVNKNLELTAKWIDAQYAPLQSVQNNWGTYGDDKQQNIFELDQASNSLKHLPLNGTAPAELRQKTEVGGPLAILDSYYGKVTTMPDDAKWRLDLIKEYYVPYMSNDNNYPRVFMTQEDLDKIAHIEADMNDYIYRKRAEWIVNGNIDTEWDDYKKELEKYGLSDYLAIKQKYYDQYQANKN
>NZ_LS483523.1|WP_054365898.1|952806_954126_+|glycoside-hydrolase-family-32-protein
MGDKKYTVEKANRFIAENKHLVNTQYKPEEHFSAEIGWINDPNGFVYFRGEYHLFYQFYPYDSVWGPMHWGHAKSKDLVTWEHLSVALAPDQDYDRNGCFSGSAIVKDDRLWLMYTGHIEEKTGVRQVQNMAFSDDGIHFEKIEQNPVATGADLPDELIAADFRDPKLFEKDGRYYSVVAAKHKDNVGCIVLLGSDNLVEWQFESIFLKGVEHQGFMWECPDYFELDGKDCLIMSPMRYQREGDSYHNINSSLLFTGKVDWREKRFIPESVQEIDHGQDFYAPQTLLDDQNRRILIAWMQTWGRTLPTHDQEHKWACAMTLPRILRLEDGKLRQFPVKKGQYQIQIDKDCHYHLGNDIDYLEFGYDSNAQQVYIDRSHLIQKILGEEEQDTSRRYVDIEAKELEVVLDKNSIEIFVNQGEASLTATYYLTVPAELSRID
>NZ_LS483523.1|WP_054365899.1|954670_955942_-|replication-associated-recombination-protein-A
MPDNLALRMRPKTIDQVIGQEHLVGPGKIIRRMVEANRLSSMILYGPPGIGKTSIASAIAGTTKYAFRTFNATVDSKKRLQEISEEAKFSGGLVLLLDEIHRLDKTKQDFLLPLLESGLVIMIGATTENPFFSVTPAIRSRVQIFELEPLSNQDVKEALQIALSNPERGFDFPIELDEDALDFIATSTNGDLRSAFNSLDLAVLSTPENDEGIRHITLDIMENSLQRSYITMDNDGDGHYDVLSALQKSIRGSDVDASLHYTARLIEAGDLPSLARRLTVIAYEDIGLANPEAQIHTVTALDAAQKIGFPEARILIANVVIDLALSPKSNSAYVAMDKALADLKTSGHLPIPRHLRDGHYSGSKELGNAQDYLYPHNYPGNWVKQDYLPEKIRNHHYFQAEDTGKYERALAQRKEAIDRLRKI
>NZ_LS483523.1|WP_000818078.1|956211_956451_+|hypothetical-protein
MKREVISNGNDGPSQEILIFTKQIRHWILSDQVISGKRKLFFREDTPKEILDLYENIKSKLDFAYQEVHSNNGLKKYEK
>NZ_LS483523.1|WP_001048906.1|956615_956795_+|hypothetical-protein
MNLIFEEYQFVKIGDKKYRVRSVPMIHSTPPQSVLDRDTFTIDYTDDELLDKEAVFTTH
>NZ_LS483523.1|WP_023396413.1|956931_957111_+|type-II-toxin-antitoxin-system-HicA-family-toxin
MPMTQKEMVKLLTAHGWIKTRGGKGSHIKMEKQGERLITIPHGELNKYTERGIRKQVGL
>NZ_LS483523.1|WP_023396412.1|957147_957600_+|type-II-toxin-antitoxin-system-HicB-family-antitoxin
MLVTYPALFYYDDTDGTEATYFVHFPDFEYSATQGEGISDALAMGSEWLGITVADLIESDGELPQPSDINSLSLIDNDPFKDDEDFVSTYDLDKSFISMVSVDVSEYLGSQEPIKKTLTIPKWADKLGREMGLNFSQTLTDAIADKKVQA
>NZ_LS483523.1|WP_023396411.1|957890_958361_+|DUF3013-family-protein
MATYGFLDVLEEELDKNFPFDFEISWDKRNHAVEVSFLLEAQNAAGVEMVDEDGEVLSDDILFEEAVLFYNPAKSTVNEEDYLTVIPYLPKKGFSREFLVYFALFLKDTAEVGLDVLMDFLEDPEAEEFVMEWNQEVFEEGKVGLEEGEFYPYPRY

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Crispr_ID: NZ_LS483523_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_LS483523_3

972628-986211

Orphan

Consensus_repeat	Method
AGNACNTCNGCANNNACA	CRT
TCNGCATCAACAAGCGCN	CRT
AGNACNTCNGCATCAACA	CRT
ACNTCNGCAAGNACNTCN	CRT

397 spacers

The CRISPR arrays of NZ_LS483523_3

>merge|NZ_LS483523|3|972628-986211|CRT,CRT,CRT,CRT
TCGGCCTCAACCAGCGCATCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACGAGTGCATCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATAAGTGCATCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCATGTCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCTTCAGCGTCGACAAGTGCGTCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCTTCAGCGTCGACAAGTGCGTCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCGGCATCAACAAGTGCAAGTACGTCAGCAAGCACATCAGCAAGCACGTCGGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCAACAAGTGCAAGTACGTCAGCAAGTACATCAGCATCAACAAGTGCAAGTACATCAGCAAGTACGTCAGCATCAACAAGCGCCAGCACGTCAGCTAGCACATCAGCCTCAACGAGCGCAAGTACATCAGCAAGTACATCAGCATCAATAAGTGCCAGCACATCAGCTTCAACAGTTACAAGTGCCTCAGACACAATGAGTACAAGTACGTCAGTAAGTACCTCTGAGTCAACAAGTACA

>NZ_LS483523|3|2|972628-982995|CRT
TCGGCCTCAACCAGCGCA	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACGAGTGCATCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACA
	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCT
	AGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACG
AGTGCA	TCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCC
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATA
	TCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATAAGTGCATCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCATG
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCATGTCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	AGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCA
	TCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACG
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCG
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGGACATCGGCTTCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGGACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
AGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACA
	AGCGCAAGTACGTCAACAAGTGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCA
	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCAGCTTCAACA	AGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCGGCATCAACAAGTGCC
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
TCGGCATCAACA	AGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGCACGTCAGCATCAACA	AGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCTTCAGCA	AGTACCAGTGCGTCGGCTTCAGCGTCGACA
AGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
	TCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACA
AGCGCCTCAGCTTCAACA	AGTGCAAGTACGTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACGTCCGCTTCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGTGCCAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCA
AGTACGTCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCATCGACAAGTGCA
	GCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGC
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	TCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCA
	GCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGC
	TCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGT
	TCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	GCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCA	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGT
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCA	GCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
AGTACGTCA	GCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCA
	TCGGCATCAACAAGTGCC
AGCACGTCAGCAAGTACA	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCA	GCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
ACAAGCGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCG
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCG	GCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCG
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGT
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGC
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGT
ACGTCAGCAAGTACGTCC	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGT
ACATCGGCAAGCACGTCA	GCATCGACAAGTGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGC
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGC
ACGTCAGCAAGCACGTCA	GCATCGACAAGTGCAAGT
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	GCATCGACAAGTGCAAGCACATCGGCGTCA
ACAAGTGCAAGTACGTCA	GCAAGTACATCGGCAAGTACGTCCGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCA
ACAAGCGCAAGTACGTCA	GCAAGTACATCGGCATCA
ACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
TCAGCATCGACAAGTGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
TCGGCGTCAACAAGTGCA	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
TCAGCGTCGACAAGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
TCAGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACAAGCGCA	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCA	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGTACG
TCCGCATCAACAAGCGCA	AGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACG
TCGGCATCAACAAGTGCA	AGTACGTCAGCAAGCACATCAGCAAGCACG
TCGGCATCAACAAGCGCA	AGTACATCGGCAAGCACG
TCAGCATCAACAAGTGCA	AGTACGTCAGCAAGTACA
TCAGCATCAACAAGTGCA	AGTACATCAGCAAGTACG
TCAGCATCAACAAGCGCC	AGCACGTCAGCTAGCACA
TCAGCCTCAACGAGCGCA	AGTACATCAGCAAGTACA
TCAGCATCAATAAGTGCC	AGCACATCAGCTTCAACAGTTACAAGTGCC
TCAGACACAATGAGTACA	AGTACGTCAGTAAGTACC


>NZ_LS483523|3|4|972628-986211|CRT
TCGGCCTCAACCAGCGCA	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACGAGTGCATCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACA
	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCT
	AGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACG
AGTGCA	TCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCC
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATA
	TCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATAAGTGCATCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCATG
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCATGTCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	AGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCA
	TCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACG
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCG
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGGACATCGGCTTCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGGACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
AGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACA
	AGCGCAAGTACGTCAACAAGTGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCA
	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCAGCTTCAACA	AGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCGGCATCAACAAGTGCC
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
TCGGCATCAACA	AGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGCACGTCAGCATCAACA	AGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCTTCAGCA	AGTACCAGTGCGTCGGCTTCAGCGTCGACA
AGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
	TCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACA
AGCGCCTCAGCTTCAACA	AGTGCAAGTACGTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACGTCCGCTTCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGTGCCAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCA
AGTACGTCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCATCGACAAGTGCA
	GCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGC
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	TCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCA
	GCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGC
	TCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGT
	TCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	GCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCA	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGT
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCA	GCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
AGTACGTCA	GCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCA
	TCGGCATCAACAAGTGCC
AGCACGTCAGCAAGTACA	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCA	GCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
ACAAGCGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCG
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCG	GCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCG
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGT
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGC
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGT
ACGTCAGCAAGTACGTCC	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGT
ACATCGGCAAGCACGTCA	GCATCGACAAGTGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGC
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGC
ACGTCAGCAAGCACGTCA	GCATCGACAAGTGCAAGT
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	GCATCGACAAGTGCAAGCACATCGGCGTCA
ACAAGTGCAAGTACGTCA	GCAAGTACATCGGCAAGTACGTCCGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCA
ACAAGCGCAAGTACGTCA	GCAAGTACATCGGCATCA
ACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
TCAGCATCGACAAGTGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
TCGGCGTCAACAAGTGCA	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
TCAGCGTCGACAAGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
TCAGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACAAGCGCA	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCA	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGTACG
TCCGCATCAACAAGCGCA	AGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACG
TCGGCATCAACAAGTGCA	AGTACGTCAGCAAGCACATCAGCAAGCACG
TCGGCATCAACAAGCGCA	AGTACATCGGCAAGCACG
TCAGCATCAACAAGTGCA	AGTACGTCAGCAAGTACA
TCAGCATCAACAAGTGCA	AGTACATCAGCAAGTACG
TCAGCATCAACAAGCGCC	AGCACGTCAGCTAGCACA
TCAGCCTCAACGAGCGCA	AGTACATCAGCAAGTACA
TCAGCATCAATAAGTGCC	AGCACATCAGCTTCAACAGTTACAAGTGCC
TCAGACACAATGAGTACA	AGTACGTCAGTAAGTACC
TCTGAGTCAACAAGTACA

>NZ_LS483523|3|1|972640-977763|CRT
AGCGCA	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACGAGTGCATCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACA
	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCT
	AGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACG
AGTGCA	TCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCC
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATA
	TCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATAAGTGCATCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCATG
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCATGTCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	AGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCA
	TCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACG
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCG
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGGACATCGGCTTCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGGACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
AGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACA
	AGCGCAAGTACGTCAACAAGTGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCA
	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCAGCTTCAACA	AGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCGGCATCAACAAGTGCC
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
TCGGCATCAACA	AGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGCACGTCAGCATCAACA	AGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCTTCAGCA	AGTACCAGTGCGTCGGCTTCAGCGTCGACA
AGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
	TCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACA
AGCGCCTCAGCTTCAACA	AGTGCAAGTACGTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACGTCCGCTTCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGTGCCAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCA
AGTACGTCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCATCGACAAGTGCA
	GCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGC
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	TCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCA
	GCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGC
	TCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGT
	TCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	GCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCA	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGT
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCA	GCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
AGTACGTCA	GCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCA
	TCGGCATCAACAAGTGCC
AGCACGTCAGCAAGTACA	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCA	GCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
ACAAGCGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCG
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCG	GCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCG
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGT
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGC
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGT
ACGTCAGCAAGTACGTCC	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGT
ACATCGGCAAGCACGTCA	GCATCGACAAGTGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGC
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGC
ACGTCAGCAAGCACGTCA	GCATCGACAAGTGCAAGT
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	GCATCGACAAGTGCAAGCACATCGGCGTCA
ACAAGTGCAAGTACGTCA	GCAAGTACATCGGCAAGTACGTCCGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCA
ACAAGCGCAAGTACGTCA	GCAAGTACATCGGCATCA
ACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
TCAGCATCGACAAGTGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
TCGGCGTCAACAAGTGCA	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
TCAGCGTCGACAAGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
TCAGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACAAGCGCA	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCA	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGTACG
TCCGCATCAACAAGCGCA	AGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACG
TCGGCATCAACAAGTGCA	AGTACGTCAGCAAGCACATCAGCAAGCACG
TCGGCATCAACAAGCGCA	AGTACATCGGCAAGCACG
TCAGCATCAACAAGTGCA	AGTACGTCAGCAAGTACA
TCAGCATCAACAAGTGCA	AGTACATCAGCAAGTACG
TCAGCATCAACAAGCGCC	AGCACGTCAGCTAGCACA
TCAGCCTCAACGAGCGCA	AGTACATCAGCAAGTACA
TCAGCATCAATAAGTGCC	AGCACATCAGCTTCAACAGTTACAAGTGCC
TCAGACACAATGAGTACA	AGTACGTCAGTAAGTACC


>NZ_LS483523|3|3|979297-984306|CRT
	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACGAGTGCATCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACA
	TCAGCCTCAGCAAGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCT
	AGTACAAGTGCCTCAGCCTCAGCATCAACGAGTGCGTCAGCTTCCGCATCAACGAGTGCGTCAGCTTCAGCAAGTACCAGTGCTTCGGCTTCCGCATCAACG
AGTGCA	TCGGCTTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCC
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGCGCGTCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATA
	TCGGCTTCAGCAAGCACCTCAGCGTCTGAATCTGCATCAACGTCTGCCTCAGCCTCAGCATCAATAAGTGCATCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGGCTTCAGCATCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACA
	TCGACAAGTGCGTCTGAATCCGCGTCAACCAGTGCCTCAGCTTCAGCAAGTACCAGTGCCTCAGCTTCAGCGTCAACAAGTGCAAGCACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCATG
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCATGTCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	AGCGCGTCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCA
	TCGACCTCAGCAAGCACATCGGCATCAACAAGTGCCAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACG
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCG
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGGACATCGGCTTCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGGACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	TCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
AGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAACAAGTGCAAGTACA
	AGCGCAAGTACGTCAACAAGTGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCA
	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCA
	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCAGCTTCAACA	AGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCA
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCGGCATCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
	AGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCGGCATCAACAAGTGCC
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACA
TCGGCATCAACA	AGCGCAAGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCA
	AGTACGTCAACAAGTGCAAGTACATCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACA
	AGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCCGCATCAACA	AGCGCAAGTACATCGGCA
AGCACGTCAGCATCGACA	AGTGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
AGCACGTCAGCATCAACA	AGCGCAAGCACGTCAGCAAGTACATCGGCGTCAACAAGTGCA
	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCTTCAGCA	AGTACCAGTGCGTCGGCTTCAGCGTCGACA
AGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
	TCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACA
AGCGCCTCAGCTTCAACA	AGTGCAAGTACGTCAGCA
AGTACATCAGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACGTCCGCTTCAACA	AGCGCGTCGACCTCAGCA
AGTACATCAGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGTGCCAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	AGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCA
AGTACGTCCGCATCAACA	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCATCGACAAGTGCA
	GCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGC
	TCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	TCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCA
	GCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGC
	TCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	TCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGT
	TCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACG
	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCA
	AGTACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCA
	GCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCAAGCACGTCAGCA
AGTACATCGGCTTCAACA	AGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCA
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCA
	GCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	AGCGCAAGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCA
	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACA	AGCGCGTCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACG
	GCATCAACAAGCGCAAGTACGTCAGCAAGCACATCAGCATCAACAAGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	AGCGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCA
	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	AGCGCGTCGACCTCAGCA
AGCACGTCA	GCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGT
	AGCGCAAGTACATCGGCA
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	AGTGCAAGTACGTCAGCA
AGTACATCGGCATCAACA	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGTACGTCAGCAAGCACGTCAGCA
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGT
	AGCGCGTCGACCTCAGCA
AGTACATCGGCATCAACA	AGCGCAAGCACGTCAGCA
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	AGTGCAAGTACATCGGCA
AGCACGTCA	GCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
	AGTGCAAGCACATCGGCGTCAACAAGTGCA
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	TCGGCAAGTACGTCCGCATCAACAAGCGCA
AGTACGTCAGCAAGTACA	TCGGCATCAACAAGCGCGTCGACCTCAGCA
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCG
	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCG
TCGACCTCAGCAAGTACA	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGTACATCGGCATCAACAAGCGCG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCA
	TCAGCATCAACAAGCGCG
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
	TCAGCAAGGACATCGGCTTCAACAAGCGCA
AGTACGTCA	GCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCA
	TCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCA
	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
	GCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCA
	TCGGCATCAACAAGTGCC
AGCACGTCAGCAAGTACA	TCGGCATCAACAAGCGCA
AGTACGTCAGCAAGTACG	TCCGCATCAACAAGCGCAAGTACATCGGCTTCAACAAGCGCG
	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	TCAGCATCAACAAGCGCG
TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCA	GCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
	AGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACG
	GCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCTTCA
ACAAGCGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCG
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCG	GCATCAACAAGCGCAAGCACGTCAGCAAGCACGTCAGCATCG
	AGCACGTCAGCAAGCACGTCAGCATCGACAAGTGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACA
	GCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGT
	AGTACGTCAGCAAGTACATCGGCAAGTACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACGTCCGCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCGACCTCAGCAAGC
	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCGTCAACAAGTGCAAGT
ACGTCAGCAAGTACGTCC	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
	GCTTCAACAAGCGCAAGT
ACATCGGCAAGCACGTCA	GCATCGACAAGTGCAAGT
ACGTCAGCAAGTACATCG	GCATCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGTACGTCAGCAAGC
	AGTACGTCAGCAAGCACGTCAGCAAGGACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGCACGTCAGCAAGCACG
	GCTTCAACAAGCGCGTCG
ACCTCAGCAAGTACATCG	GCATCAACAAGCGCAAGC
ACGTCAGCAAGCACGTCA	GCATCGACAAGTGCAAGT
	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGCACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACATCGGCAAGTACG
	GCATCGACAAGTGCAAGCACATCGGCGTCA
ACAAGTGCAAGTACGTCA	GCAAGTACATCGGCAAGTACGTCCGCATCA
ACAAGCGCA	AGTACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
	GCAAGTACATCGGCATCA
ACAAGCGCAAGTACGTCA	GCAAGTACATCGGCATCA
ACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCGTCAACAAGTGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCGGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCAAGTACATCGGCTTCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACATCGGCAAGCACG
TCAGCATCGACAAGTGCA	AGTACATCGGCAAGCACGTCAGCATCGACAAGTGCAAGTACGTCAGCAAGTACATCGGCATCAACAAGTGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGTACATCAGCATCAACAAGCGCAAGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGCACGTCAGCATCAACAAGCGCAAGCACGTCAGCAAGTACA
TCGGCGTCAACAAGTGCA	AGTACGTCCGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCTTCAGCAAGTACCAGTGCGTCGGCT
TCAGCGTCGACAAGTGCG	TCAGCTTCTGAATCGGCATCAACGAGTGCCTCAGCCTCAGCAAGCACAAGCGCCTCAGCTTCAACAAGTGCAAGTACGTCAGCAAGTACA
TCAGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGGACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACGTCCGCTTCAACAAGCGCGTCGACCTCAGCAAGTACA
TCAGCATCAACAAGCGCA	AGCACGTCAGCAAGTACATCGGCATCAACAAGTGCCAGCACGTCAGCAAGTACATCGGCATCAACAAGCGCAAGTACGTCAGCAAGTACG
TCCGCATCAACAAGCGCA	AGTACATCGGCTTCAACAAGCGCGTCGACCTCAGCAAGTACATCAGCATCAACAAGCGCGTCGACCTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGCACGTCCGCATCAACAAGCGCAAGTACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCTTCAACAAGCGCAAGTACATCGGCAAGTACG
TCCGCATCAACAAGCGCA	AGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCG	TCGACCTCAGCAAGCACGTCAGCAAGTACA
TCGGCATCAACAAGCGCA	AGTACGTCAGCAAGTACG
TCGGCATCAACAAGTGCA	AGTACGTCAGCAAGCACATCAGCAAGCACG
TCGGCATCAACAAGCGCA	AGTACATCGGCAAGCACG
TCAGCATCAACAAGTGCA	AGTACGTCAGCAAGTACA
TCAGCATCAACAAGTGCA	AGTACATCAGCAAGTACG
TCAGCATCAACAAGCGCC	AGCACGTCAGCTAGCACA
TCAGCCTCAACGAGCGCA	AGTACATCAGCAAGTACA
TCAGCATCAATAAGTGCC	AGCACATCAGCTTCAACAGTTACAAGTGCC
TCAGACACAATGAGTACA	AGTACGTCAGTAAGTACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LS483523.1\|WP_001029580.1\|969132_969447_-\|thioredoxin	unknown	unknown	gnl\|CDD\|200072
NZ_LS483523.1\|WP_023396406.1\|968065_968245_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_000066414.1\|999800_1001333_+\|accessory-Sec-system-protein-Asp2	unknown	unknown	gnl\|CDD\|274739
NZ_LS483523.1\|WP_054365908.1\|990163_991321_+\|glycosyl-hydrolase-family-8	unknown	unknown	gnl\|CDD\|133037
NZ_LS483523.1\|WP_054365910.1\|995606_996614_+\|sugar-transferase	unknown	unknown	gnl\|CDD\|236626
NZ_LS483523.1\|WP_054365907.1\|988947_990195_+\|glycosyl-hydrolase-family-8	unknown	unknown	gnl\|CDD\|133037
NZ_LS483523.1\|WP_054370044.1\|992364_995598_+\|SP_1767-family-glycosyltransferase	unknown	unknown	gnl\|CDD\|163440
NZ_LS483523.1\|WP_000514210.1\|970541_971003_+\|transposase	unknown	unknown	gnl\|CDD\|279973
NZ_LS483523.1\|WP_111683447.1\|969782_970163_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_LS483523.1\|WP_001864907.1\|966470_967262_+\|DUF2785-domain-containing-protein	unknown	unknown	gnl\|CDD\|371322
NZ_LS483523.1\|WP_078372908.1\|991325_992168_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|366154
NZ_LS483523.1\|WP_000714845.1\|967372_968041_+\|aquaporin	unknown	unknown	gnl\|CDD\|238204
NZ_LS483523.1\|WP_069287054.1\|969462_969684_-\|DUF4649-family-protein	unknown	unknown	gnl\|CDD\|339492
NZ_LS483523.1\|WP_054365911.1\|998236_999811_+\|accessory-Sec-system-protein-Asp1	unknown	unknown	gnl\|CDD\|293598
NZ_LS483523.1\|WP_000727917.1\|996721_997948_+\|accessory-Sec-system-protein-translocase-subunit-SecY2	unknown	unknown	gnl\|CDD\|237095
NZ_LS483523.1\|WP_075286760.1\|970473_970575_+\|transposase	unknown	unknown	unknown
NZ_LS483523.1\|WP_000966495.1\|964536_965307_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_LS483523.1\|WP_054365906.1\|988066_988945_+\|exopolysaccharide-biosynthesis-protein	unknown	unknown	gnl\|CDD\|100053
NZ_LS483523.1\|WP_054374530.1\|987099_987978_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|366154
NZ_LS483523.1\|WP_000475587.1\|965299_966064_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|130358

Protein	Function_ID	Function_description	E-value
NZ_LS483523.1\|WP_001029580.1\|969132_969447_-\|thioredoxin	gnl\|CDD\|200072	TIGR01068, Thioredoxin-like_protein_slr0233, thioredoxin. Several proteins, such as protein disulfide isomerase, have two or more copies of a domain closely related to thioredoxin. This model is designed to recognize authentic thioredoxin, a small protein that should be hit exactly once by this model. Any protein that hits once with a score greater than the second (per domain) trusted cutoff may be taken as thioredoxin. [Energy metabolism, Electron transport].	2.87987e-41
NZ_LS483523.1\|WP_054365910.1\|995606_996614_+\|sugar-transferase	gnl\|CDD\|236626	PRK09814, PRK09814, sugar transferase.	8.70607e-142
NZ_LS483523.1\|WP_000066414.1\|999800_1001333_+\|accessory-Sec-system-protein-Asp2	gnl\|CDD\|274739	TIGR03712, acc_sec_asp2, accessory Sec system protein Asp2. This protein is designated Asp2 because, along with SecY2, SecA2, and other proteins it is part of the accessory secretory protein system. The system is involved in the export of serine-rich glycoproteins important for virulence in a number of Gram-positive species, including Streptococcus gordonii and Staphylococcus aureus. This protein family is assigned to transport rather than glycosylation function, but the specific molecular role is unknown. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	0
NZ_LS483523.1\|WP_054365908.1\|990163_991321_+\|glycosyl-hydrolase-family-8	gnl\|CDD\|133037	cd04194, GT8_A4GalT_like, A4GalT_like proteins catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The members of this family of glycosyltransferases catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The enzymes exhibit broad substrate specificities. The known functions found in this family include: Alpha-1,4-galactosyltransferase, LOS-alpha-1,3-D-galactosyltransferase, UDP-glucose:(galactosyl) LPS alpha1,2-glucosyltransferase, UDP-galactose: (glucosyl) LPS alpha1,2-galactosyltransferase, and UDP-glucose:(glucosyl) LPS alpha1,2-glucosyltransferase. Alpha-1,4-galactosyltransferase from N. meningitidis adds an alpha-galactose from UDP-Gal (the donor) to a terminal lactose (the acceptor) of the LOS structure of outer membrane. LOSs are virulence factors that enable the organism to evade the immune system of host cells. In E. coli, the three alpha-1,2-glycosyltransferases, that are involved in the synthesis of the outer core region of the LPS, are all members of this family. The three enzymes share 40 % of sequence identity, but have different sugar donor or acceptor specificities, representing the structural diversity of LPS.	9.60849e-62
NZ_LS483523.1\|WP_000514210.1\|970541_971003_+\|transposase	gnl\|CDD\|279973	pfam01710, HTH_Tnp_IS630, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family includes insertion sequences from Synechocystis PCC 6803 three of which are characterized as homologous to bacterial IS5- and IS4- and to several members of the IS630-Tc1-mariner superfamily.	9.93428e-05
NZ_LS483523.1\|WP_054370044.1\|992364_995598_+\|SP_1767-family-glycosyltransferase	gnl\|CDD\|163440	TIGR03728, glyco_access_1, glycosyltransferase, SP_1767 family. Members of this protein family are putative glycosyltransferases. Some members are found close to genes for the accessory secretory (SecA2) system, and are suggested by Partial Phylogenetic Profiling to correlate with SecA2 systems. Glycosylation, therefore, may occur in the cytosol prior to secretion.	3.59272e-127
NZ_LS483523.1\|WP_069287054.1\|969462_969684_-\|DUF4649-family-protein	gnl\|CDD\|339492	pfam15507, DUF4649, Domain of unknown function (DUF4649). This family of Firmicute sequences has members that are annotated as ribose-phosphate pyrophosphokinase; however there is no evidence for this attribution. Member proteins are all shorter than 100 residues in length.	1.4534e-31
NZ_LS483523.1\|WP_111683447.1\|969782_970163_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.77849e-12
NZ_LS483523.1\|WP_001864907.1\|966470_967262_+\|DUF2785-domain-containing-protein	gnl\|CDD\|371322	pfam10978, DUF2785, Protein of unknown function (DUF2785). Some members in this family are annotated as hypothetical membrane spanning proteins however this cannot be confirmed. The family has no known function.	6.77593e-23
NZ_LS483523.1\|WP_078372908.1\|991325_992168_+\|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.	3.68365e-38
NZ_LS483523.1\|WP_000714845.1\|967372_968041_+\|aquaporin	gnl\|CDD\|238204	cd00333, MIP, Major intrinsic protein (MIP) superfamily. Members of the MIP superfamily function as membrane channels that selectively transport water, small neutral molecules, and ions out of and between cells. The channel proteins share a common fold: the N-terminal cytosolic portion followed by six transmembrane helices, which might have arisen through gene duplication. On the basis of sequence similarity and functional characteristics, the superfamily can be subdivided into two major groups: water-selective channels called aquaporins (AQPs) and glycerol uptake facilitators (GlpFs). AQPs are found in all three kingdoms of life, while GlpFs have been characterized only within microorganisms.	1.56733e-52
NZ_LS483523.1\|WP_054365906.1\|988066_988945_+\|exopolysaccharide-biosynthesis-protein	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	3.19425e-37
NZ_LS483523.1\|WP_054365911.1\|998236_999811_+\|accessory-Sec-system-protein-Asp1	gnl\|CDD\|293598	pfam16993, Asp1, Accessory Sec system protein Asp1. Asp1, along with SecY2, SecA2, and other proteins forms part of the accessory secretory protein system. The system is involved in the export of serine-rich glycoproteins important for virulence in a number of Gram-positive species, including Streptococcus gordonii and Staphylococcus aureus. This protein family is assigned to transport rather than glycosylation function, but the specific molecular role is unknown. Asp1 is predicted to be cytosolic.	5.20777e-172
NZ_LS483523.1\|WP_000727917.1\|996721_997948_+\|accessory-Sec-system-protein-translocase-subunit-SecY2	gnl\|CDD\|237095	PRK12417, secY, preprotein translocase subunit SecY; Reviewed.	1.15982e-139
NZ_LS483523.1\|WP_054374530.1\|987099_987978_+\|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.	2.12702e-38
NZ_LS483523.1\|WP_000966495.1\|964536_965307_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	5.84801e-82
NZ_LS483523.1\|WP_000475587.1\|965299_966064_+\|ABC-transporter-permease	gnl\|CDD\|130358	TIGR01291, Nodulation_protein_J, ABC-2 type transporter, NodJ family. Nearly all members of this subfamily are NodJ which, together with NodI (TIGR01288), acts to export a variety of modified carbohydrate molecules as signals to plant hosts to establish root nodules. The seed alignment includes a highly divergent member from Azorhizobium caulinodans that is, nonetheless, associated with nodulation. This model is designated as subfamily in part because not all sequences derived from the last common ancestral sequence of Rhizobium sp. and Azorhizobium caulinodans NodJ are necessarily nodulation proteins. [Cellular processes, Other, Transport and binding proteins, Other].	2.92244e-38
NZ_LS483523.1\|WP_054365907.1\|988947_990195_+\|glycosyl-hydrolase-family-8	gnl\|CDD\|133037	cd04194, GT8_A4GalT_like, A4GalT_like proteins catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The members of this family of glycosyltransferases catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The enzymes exhibit broad substrate specificities. The known functions found in this family include: Alpha-1,4-galactosyltransferase, LOS-alpha-1,3-D-galactosyltransferase, UDP-glucose:(galactosyl) LPS alpha1,2-glucosyltransferase, UDP-galactose: (glucosyl) LPS alpha1,2-galactosyltransferase, and UDP-glucose:(glucosyl) LPS alpha1,2-glucosyltransferase. Alpha-1,4-galactosyltransferase from N. meningitidis adds an alpha-galactose from UDP-Gal (the donor) to a terminal lactose (the acceptor) of the LOS structure of outer membrane. LOSs are virulence factors that enable the organism to evade the immune system of host cells. In E. coli, the three alpha-1,2-glycosyltransferases, that are involved in the synthesis of the outer core region of the LPS, are all members of this family. The three enzymes share 40 % of sequence identity, but have different sugar donor or acceptor specificities, representing the structural diversity of LPS.	4.49601e-67

>NZ_LS483523.1|WP_000514210.1|970541_971003_+|transposase
MGKERRKQGNLERKKRVVKKRKIPLEELKAFVEAHPDAFLREIAARFDCALPSVWAVLKQIKVILKKTTSFREQKPEKVSEFLDILDNLKDLPVLYIDETGIDRYLYRPYAGAPRGEKVYGKISGRRFERTNEVEQKLNGSFLIRYIDSQIRE
>NZ_LS483523.1|WP_075286760.1|970473_970575_+|transposase
MKGGHRHVEAAKVFDVGVRTLFTWEKKDVNKGT
>NZ_LS483523.1|WP_111683447.1|969782_970163_-|MarR-family-transcriptional-regulator
MTYLEKLFDFNRRQKEIESLLEETIAQQSEQSLTLKEFYLLYYLDLAEEKSLRQIDLPDKLHLSPSAVSRMVARLEAKNCGLLSRMCCHQDRRSSFICLTNDGQKTLASLQKTVEESLEAGLDFLI
>NZ_LS483523.1|WP_069287054.1|969462_969684_-|DUF4649-family-protein
MIEITYIDTSKNERTVTFESYEDFERSQQACLIGVADYYPVQKLTYKGHNLDYHGTYGDIFFYLMKQDLSQYN
>NZ_LS483523.1|WP_001029580.1|969132_969447_-|thioredoxin
MAKAITDATFEQETKDGLVLVDFWATWCGPCRMQGPILDKLSEELSEDVLKIVKMDVDENPNTARAFGIMSIPTLLFKKDGQVVKQVAGVHTAEQIKAIIAELS
>NZ_LS483523.1|WP_023396406.1|968065_968245_-|hypothetical-protein
MLKAVFEVIDKTDEVSSKHCFEVVDRTDEVSNHTYGKVKLTWFEEIFEEYHTKKPCSSR
>NZ_LS483523.1|WP_000714845.1|967372_968041_+|aquaporin
MKKFVAELIGTFMLVFVGTGAVVFGNGLDGLGHLGIAFAFGLAIVVAAYSIGTVSGAHLNPAVSIAMFVNKRLSSSELVNYILGQVVGAFIASGAVFFLLANSGMSTASLGENALANGVTVFGGFLFEVIATFLFVLVIMTVTSESKGNGAIAGLVIGLSLMAMILVGLKITGLSVNPARSLAPAVLVGGAALQQVWIFILAPIAGGVLAALVAKNFLGTEE
>NZ_LS483523.1|WP_001864907.1|966470_967262_+|DUF2785-domain-containing-protein
MYQDLLRKIAEEKPNYNQEEIQWLLDHLGDPSPEIRDDLVFTSFAKEIQEELFTQEQFHFIAEVVLADGGLDKEIDKVGLSTLERSFRALIYANLLSADANQQSVFYQGLQSEIRNVLLNQGLHYLSKEKDTTGFSSQYGWVHSFAHGADLLKEVVCHPDFPKNRVHEVFDILGQLFKRMSIRFTDDEDWRLARVIYEPILQGKLEQEQVASWIKTVDFPIEEREDFYKFSNFRSCLVEVYVQLDQRNSLQDELKEAIQSFQY
>NZ_LS483523.1|WP_000475587.1|965299_966064_+|ABC-transporter-permease
MFKLSFHSIGHVVVRNYMSFRNLFKISIVPNLIDPLFYLLAMGFGVGAYLTHVNGMLYRDFVITGLIAATAMSAATAETTVNAFIQYKIEKTYDAMLMTPINTNDIVVGQAIWAGIRAVIFGGIFWLISILITAHFHVLMLLIPLILFIVGYLFGVLGLIFTYLAPSREFLNYYNVLAIRPLYMFSDTFFPITSLPPILGDLTWFSPLYHATRMIRIIWGGEVTGLYLHLIWLIALALLITVLPMYMLHRRYYR
>NZ_LS483523.1|WP_000966495.1|964536_965307_+|ABC-transporter-ATP-binding-protein
MLYLWGKERVKKLSVKNLKKQYGSYEAVKGISFELGEGECLGILGINGAGKTSTLKMIYSLTSISSGEIDILGQNIETNRRKSKSCLGIVGQEDMLDMTLNVYDNLFAHGLCYGISSVELRKRIDSLLDFVQLSKHAQKMVNQLSGGMRRRLVLARALINRPDIIILDEPTVGLDIQSRNIIWDKLLELKELGVSIIITSHYMNEIEYLTDRVLMLHQGTIKEEGTVEDLLIKYDADNLETLFLGLTGTEKEDLHV
>NZ_LS483523.1|WP_054374530.1|987099_987978_+|glycosyltransferase-family-2-protein
MKDLVSVVIPVYNVENYLEECIQSVLNQTYTNLDIVLVNDGSTDASAEICDRFAEIDGRVRVFHTENRGAALSKNFGVTQALGEYVLFVDSDDIAEKRMVETLYRQVEETGADIVIGNYFLYDENDGQCKFYVLERDFCIEELSAQELIDRQAGKWHLNASAFIMPMFKLFKKDLLLQVPFTNGRRFDDEATIHRLFIKSQKTIFVNDNLYIYRVRQGSIMTSRFDISWVQDILQVFSSKLADLLLAGVDTSVMRIRFVNILKEYKYLCETYNLTHTDEYREILFRLDLYRE
>NZ_LS483523.1|WP_054365906.1|988066_988945_+|exopolysaccharide-biosynthesis-protein
MDLNVPINFQGNYHQVEISEGALLQIGQGVTMRSFTSLEVNEGAKLSIGDRVFFNDHCSIRCGKEIEIGKDTMFGDGVRIFDSNHRYSNYHVEKLRFNCEKITIGNNCWIGSNVVILKGVSIGDNVIIGANALIYRDIPADSIVTSEQNLRITPRKNYYYHAFTLTASDTLEELEFLVTELSDVAFHIVAKTNISPYLEKFDQFDNVNLYTNIHHNDIIEDLLTRSDIYLDINHWEEVDGIVGRAIEKGKKIFAFSNVVHRISDDIQVFKIEEKNKMVEAIRQQLEKDDNGD
>NZ_LS483523.1|WP_054365907.1|988947_990195_+|glycosyl-hydrolase-family-8
MIGNNIQSKKAIALGADSNYMDKVETTIKSVCSHNRDIKFYIFNSDFPTEWFQLMNKRLAVLNSEIVNVKITDDTINHFNLPTPHLSSAAYLRYFILNFVNEKRILYLDSDIVVTSSLVSLFESSLDGQPMGAVPDLPNTYDGFNSGVLVIDTDMWRKENISKKLLDLTVEHHEHVYGDQEILNMFFKDRWKQFDLTFNLQVGADAHQYYMGDYDWYESFEGVPCIIHYTTENKPWKHFRFNRFRDIWWFYYGLNWNDILLRTHVLKETFAELISPISQHASIFTNTGDIEGIGYLLEKLPDVQFHIVAPTYFSPNIIELQRYSNCYIYPCADPKMKQNIIDKTDIYLDINYGLGMDQELQEMARQGKAIYSFDSTNHFSNGESTVFTVGEIDELIRKIEELGDNNESKSDCSWS
>NZ_LS483523.1|WP_054365908.1|990163_991321_+|glycosyl-hydrolase-family-8
MNQKVIALGADIHYLDKVETVIKSVSVHNHKVKFYVFNDDLPSEWFLLMRNRLKVIGSEIINVKKADHNLRDFHLPNAILSYAAFFRYFIADEVIEDRVLYLDSDTIVNAKLDDLFFLDLQGYSIAAVQDFDQDGWLTTFNAGMLLIDAKKWREKKSTQNLLELTAQHHEHVYGDQGVLNIYFGDQWLHLDKEYNFMVGLDQFLHLKGNADWYQSNYYGNYEPKIVHYTTEFKPWTHLTLTRFRKLWWFYYGLNWNDVLLSSDIVKRSFKELVGVPLYHTCIFTNSAAMESLEYLLSELPEVHFTILAHTNFNSFNMKETLDKMDFYLDINHEGEIVNIIEEVCRRNKPIFGFDNTSHDSKGRSQIFSSTEPNKMVEAIRQFIGE
>NZ_LS483523.1|WP_078372908.1|991325_992168_+|glycosyltransferase-family-2-protein
MADELISIVVPIYNVENYLRMCLDSIQNQTYQNFECLLINDDSPDNSAEICREYVAKDSRFRYFEKENGGLSSARNYGIERAEGTVITFVDSDDWLEGNSLEILYDKMNQYDADVVVSCYCIYDEEKETFLFFTYGETYDKIYSTKELLEMLPVLEGKTLSFQTSWGILFKKELFEHISFPVGKINEDIATNYKCYMQAKKIVYAHKNTYCYRLRNTSISHASFTEKMMRDDHDARIERIALLALKGYDISNYLTQHKQYLKAWHAHAIDIAEKQLVWRN
>NZ_LS483523.1|WP_054370044.1|992364_995598_+|SP_1767-family-glycosyltransferase
MKAIVLAGDKNYLTPMLTTIKSILYYNQQVKIYILHQNIPSDWFHELKIQVEKLGSVVEGIYIGDTIDVEWKTQEHISPIAYARYLIPRLIKEERVIYLDSDIIVNGDLSSLFELDFGDYSIAAVRDADGNGFNSGVLVIDSQKWREKDVTSILFDKTVEYMSYLDHTDTDRFNGDQTIFNLVFQNHWLELDKRFNLQVGHDVIAFYSHWDSHFELDEEPLIIHYTTYRKPWTTLMGYRYRDLWWSFHDVTFDQISDHYQGRFAVKRVYDFHDINLFTFTDSQDFLYIEELAQTLPNIGFHIGAYTDMGDILLALDKYPNVYLYPSMVGAVIDEMIEKSDAYLDIHKGSPMNFIVNRYTSADRPVLTFDVTNKNQLEQIVISSQSPQPMIEAIKELKKDKMDMKAIVLGANYQYADKVLTTIKSICCHNRGLRFYLINSDFPTEWFYNLNRKLKELDCEIVNARVNSSHISQYKTNIHYTTFLRYFISDFVEEDKVLYLDCDLVVTRDLSPLFDVELGDYPLAAVKDLGAQVYFNEHGFNAGVLLINNRLWKQEEVRKQLIEMTNELHDKVAQDDQSILNLLFKDRWLVLDFKYNCITLHTHFSDYRPESGTYPPIIHYLTERKPWGLYERSIYRDVWWYYNAQDWSDIGEATPCLTKDQVSQYTGVQHSGVQHSAFIYTFSCDLRNIECLIEGLPNVKFYIAAPVMVADSITDLLAYPNVSVLSDIAGQPPLIDSLVEGCDFLLDINADIEVDGIIERFRQAGKPVFAFESVVHGEQGQFLYDQAHPEEMVLAIEAYCQNGELPVKKLKSYPKVLDIQQSLDYILEHHFSVIRYGDGEMDIMMGHGIPYQDYDENLAEQLRSMIQLESSPELLVCLSDVFEGLERYNPEAVNFWQEHLEHYKEAYHRFCTASFYGSTFISRPYMDLKDKTASVAHFEKLKQLWDERDILIVEGENSRSGVGNDLFDNARSVERIICPSRNAYGKVQVIQEAVEKYADGKLVFLMLGPTAKVLAYHLSQKGIQAIDLGHVDSEYEWFKMGATSKVKFSHKHTAEHNFDQEIQFVEDEIYNKQVVVRI
>NZ_LS483523.1|WP_054365910.1|995606_996614_+|sugar-transferase
MKINITNIYGMSGQSTALIAQNETVKIAKKLDFHELSFYFYNIYSDSEGELNSRLDGVLAKLGYGDIVVYQSPTWNGREYDQNFIRKCKILNTKMITFIHDVPPLMFPSNYYLMPEYIEMYNQSDLVVVPSEKMKERLIQEGLTVQKIIIQGMWDHVHNYPLKQPSFQKKLYFAGSVERFEHLSNWAYSTPLDIFSESNYENSNPRVSFKGWKTDPELLFALSEGGFGLVWGTSENPADEEDYYRLNISHKVSTYLAAGIPVVVPSYLSNASFIKEKGLGYVVDSLEEANRLVEETTAEFYQQMVKNVSKVSYALKEGYFTKKLLIDAVMQLLDI
>NZ_LS483523.1|WP_000727917.1|996721_997948_+|accessory-Sec-system-protein-translocase-subunit-SecY2
MKKKLKSVVVKRVMWTICFIFVYILGSRLTLPFVNVNDTSFLGGNAAFLAFSTAMTGGNLRSLSLFSVGLSPWMSAMILWQMFSMSKKLGLGNLPLEIQERRKMILTFIISFIQTLAITLNLPIQEGVNHDLVLILNILLLISGTFFLVWLSDLNSLLGVGGSVVILMSSMIVSVPENIVRSIIDLHVNLLFIISLLLISIAFLYIAVRVQKARYRILVNKIMIHNRFKRYSYFDIMLNPAGGMPFMYAISLVSIPQYLLMLLHIFVPKTRWVDNWIAEFTIGRPVWVYTYIIVLFLLGIAFAFVNMNGEQIADKMKKSGEYIYDIYPGEDTALYINRLVLRFAVIGSIYILLMAGIPMLIILYEPRYMQLSMLPGLFLMFNGMIFNVKEEINALTLNESYRPLVERK
>NZ_LS483523.1|WP_054365911.1|998236_999811_+|accessory-Sec-system-protein-Asp1
MYYFIPFLESMNQSWQVDIVPWYQTTHRLEFDDVLHQIRIFKREGIKSKIVLLPYHPHMRYLLHRQDLLEVEAFSVFDAIQDIENEEIYPLQLKDLAWDEDCDFIYTPFLIAVKQKGELHAHIEFGTEGFISYITYFKDNQVDFICYFDDRGFLSSLVKYQDNQAVSRYYYNSNAEWQIKEYLQGIHTKVEVNPRFSHRFRKSTYQSVDEVVWEFFEKFLTAEYKEGESFVLAAQTKYQNQLLKHLPEHADKILTFFIERNQEDDLNLHHQAVKQAKILISDRQDFLERLKQHYPQFTYKMHHLPSFDTRLKLGVSQRVKESKLYVQLDLNTPFNSEALYEVLNFVSQNPLTEIVFATFNAEGYQIEALQKHLFTLISERLNFRDLLKESIISGAENKLEENKEENYRFQIVNLNDEIGLIRELEYTRLIVDLNPIANIYTQIAGISAGIPQINLSESEYVTHLQNGYILSDLSEFSKAGHYFLDTLEHWNQALIHSIDKIRQNTGNQFVQKWERWLEEAKSEQ
>NZ_LS483523.1|WP_000066414.1|999800_1001333_+|accessory-Sec-system-protein-Asp2
MSNKLHILQIGNRNWSHYYEIPENIEWHFFWPGSTTAIKKVMKMEGIRTFSGVVIENPDYLPDLLPLINILTPYTIFYSDICASYSPLVEEFLKKTCAQVTDFSNPRELLRILSKALFKGQYGDKLTPIDMVVNPYFAGSIRYNGYENLELVGSYGEDFRPLISWKYNIRASEWNPIELWLEYEKDLSCDIRIVVRNIQDGSTADFIKERIFTTDDMEAAILLDDDFSSFISVSLEAKGNGRLKIGALHQRLTRYQFGKFVLGGNIIRSKNREEINYFFYPGDFKPPLNVYFSGYRRAEGFEGFGMMKSLGSPFLLFQDPRIDGGAFYLGDDDFENAVRRVIQHHLDLLGFSNKELILSGISMGTYGALYYSSDFEPKAVIVSKPLTNLGLIAERGRLEAPGLFPTAFDILRHHSQGKADIDSINILNARFWERFRGADFNQTIFGLSYMKEEDYDPIAYDSLVDSLYSTGARIMVKGTSGRHNDDNDSTILWFVNFYKMVLEQEFGRKY

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Crispr_ID: NZ_LS483523_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_LS483523_4

1547443-1547525

Orphan

Consensus_repeat	Method
TTCTGGTGTCTGCCACCGCTTGGCCCTTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_LS483523_4

>merge|NZ_LS483523|4|1547443-1547525|CRISPRCasFinder
TTCTGGTGTCTGCCACCGCTTGGCCCTTACGTCCAAGATTGCTATCGGATTTCGTTCTGGTGTCCGCCACCGCTTGGCCCTTA

>NZ_LS483523|4|3|1547443-1547525|CRISPRCasFinder
TTCTGGTGTCTGCCACCGCTTGGCCCTTA	CGTCCAAGATTGCTATCGGATTTCG
TTCTGGTGTCCGCCACCGCTTGGCCCTTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LS483523.1\|WP_025172692.1\|1538619_1538796_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_023396278.1\|1538882_1539065_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_023396277.1\|1539567_1539750_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_023396268.1\|1555958_1556768_-\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	unknown	unknown	gnl\|CDD\|378065
NZ_LS483523.1\|WP_023396275.1\|1540217_1540502_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_023396273.1\|1547720_1547885_+\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_016397470.1\|1539227_1539410_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_016397473.1\|1535586_1537602_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226957
NZ_LS483523.1\|WP_023396274.1\|1546847_1547258_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_000821278.1\|1557487_1558075_-\|CPBP-family-intramembrane-metalloprotease	unknown	unknown	gnl\|CDD\|376806
NZ_LS483523.1\|WP_000627868.1\|1554946_1555189_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_001054257.1\|1554075_1554930_-\|conjugal-transfer-protein-TrbL	unknown	unknown	unknown
NZ_LS483523.1\|WP_075575678.1\|1539904_1540225_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_023396270.1\|1548529_1551343_-\|CHAP-domain-containing-protein	unknown	unknown	gnl\|CDD\|380090
NZ_LS483523.1\|WP_000227921.1\|1556767_1557358_-\|type-IV-toxin-antitoxin-system-AbiEi-family-antitoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|379128
NZ_LS483523.1\|WP_001097589.1\|1553662_1554022_-\|PrgI-family-protein	unknown	unknown	gnl\|CDD\|378907
NZ_LS483523.1\|WP_000824174.1\|1551354_1553712_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274279
NZ_LS483523.1\|WP_023396803.1\|1537614_1538349_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213222
NZ_LS483523.1\|WP_000840778.1\|1558077_1558311_-\|hypothetical-protein	unknown	unknown	unknown
NZ_LS483523.1\|WP_016397474.1\|1533931_1535506_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340394

Protein	Function_ID	Function_description	E-value
NZ_LS483523.1\|WP_023396270.1\|1548529_1551343_-\|CHAP-domain-containing-protein	gnl\|CDD\|380090	pfam18013, Phage_lysozyme2, Phage tail lysozyme. This domain has a lysozyme like fold. It is found in the tail protein of various phages probably giving them the ability to degrade the host cell wall peptidoglycan layer.	3.50626e-35
NZ_LS483523.1\|WP_023396803.1\|1537614_1538349_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	2.06921e-107
NZ_LS483523.1\|WP_001097589.1\|1553662_1554022_-\|PrgI-family-protein	gnl\|CDD\|378907	pfam12666, PrgI, PrgI family protein. This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 116 and 146 amino acids in length. This protein is found in an operon that is part of a Type IV secretion system.	8.01688e-15
NZ_LS483523.1\|WP_000821278.1\|1557487_1558075_-\|CPBP-family-intramembrane-metalloprotease	gnl\|CDD\|376806	pfam02517, Abi, CAAX protease self-immunity. Members of this family are probably proteases (after a isoprenyl group is attached to the Cys residue in the C-terminal CAAX motif of a protein to attach it to the membrane, the AAX tripeptide being removed by one of the CAAX prenyl proteases). The family contains the CAAX prenyl protease. The proteins contain a highly conserved Glu-Glu motif at the amino end of the alignment. The alignment also contains two histidine residues that may be involved in zinc binding. While they are involved in membrane anchoring of proteins in eukaryotes, little is known about their function in prokaryotes. In some known bacteriocin loci, Abi genes have been found downstream of bacteriocin structural genes where they are probably involved in self-immunity. Investigation of the bacteriocin-like loci in the Gram positive bacteria locus from Lactobacillus sakei 23K confirmed that the bacteriocin-like genes (sak23Kalphabeta) exhibited antimicrobial activity when expressed in a heterologous host and that the associated Abi gene (sak23Ki) conferred immunity against the cognate bacteriocin. Interestingly, the immunity genes from three similar systems conferred a high degree of cross-immunity against each other's bacteriocins, suggesting the recognition of a common receptor. Site-directed mutagenesis demonstrated that the conserved motifs constituting the putative proteolytic active site of the Abi proteins are essential for the immunity function of Sak23Ki - thus a new concept in self-immunity.	7.78499e-08
NZ_LS483523.1\|WP_023396268.1\|1555958_1556768_-\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	gnl\|CDD\|378065	pfam08843, AbiEii, Nucleotidyl transferase AbiEii toxin, Type IV TA system. This family was recently identified as belonging to the nucleotidyltransferase superfamily. AbiEii is the cognate toxin of the type IV toxin-antitoxin 'innate immunity' bacterial abortive infection (Abi) system that protects bacteria from the spread of a phage infection. The Abi system is activated upon infection with phage to abort the cell thus preventing the spread of phage through viral replication. There are some 20 or more Abis, and they are predominantly plasmid-encoded lactococcal systems. TA, toxin-antitoxin, systems on plasmids function by killing cells that lose the plasmid upon division. AbiE phage resistance systems function as novel Type IV TAs and are widespread in bacteria and archaea. The cognate antitoxin is pfam13338.	4.70232e-26
NZ_LS483523.1\|WP_000227921.1\|1556767_1557358_-\|type-IV-toxin-antitoxin-system-AbiEi-family-antitoxin-domain-containing-protein	gnl\|CDD\|379128	pfam13338, AbiEi_4, Transcriptional regulator, AbiEi antitoxin. AbiEi_4 is the cognate antitoxin of the type IV toxin-antitoxin 'innate immunity' bacterial abortive infection (Abi) system that protects bacteria from the spread of a phage infection. The Abi system is activated upon infection with phage to abort the cell thus preventing the spread of phage through viral replication. There are some 20 or more Abis, and they are predominantly plasmid-encoded lactococcal systems. TA, toxin-antitoxin, systems on plasmids function by killing cells that lose the plasmid upon division. AbiE phage resistance systems function as novel Type IV TAs and are widespread in bacteria and archaea. The cognate antitoxin is pfam13338.	0.00122728
NZ_LS483523.1\|WP_000824174.1\|1551354_1553712_-\|hypothetical-protein	gnl\|CDD\|274279	TIGR02746, hypothetical_protein, type-IV secretion system protein TraC. The protein family described here is common among the F, P and I-like type IV secretion systems. Gene symbols include TraC (F-type), TrbE/VirB4 (P-type) and TraU (I-type). The protein conyains the Walker A and B motifs and so is a putative nucleotide triphosphatase.	1.32703e-14
NZ_LS483523.1\|WP_016397474.1\|1533931_1535506_-\|ATP-binding-protein	gnl\|CDD\|340394	cd16917, HATPase_UhpB-NarQ-NarX-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Escherichia coli UhpB, NarQ and NarX, and Bacillus subtilis YdfH, YhcY and YfiJ. This family includes the histidine kinase-like ATPase (HATPase) domains of various histidine kinases (HKs) of two-component signal transduction systems (TCSs) such as Escherichia coli UhpB, a HK of the UhpB-UhpA TCS, NarQ and NarX, HKs of the NarQ-NarP and NarX-NarL TCSs, respectively, and Bacillus YdfH, YhcY and YfiJ HKs, of the YdfH-YdfI, YhcY-YhcZ and YfiJ-YfiK TCSs, respectively. In addition, it includes Bacillus YxjM, ComP, LiaS and DesK, HKs of the YxjM-YxjML, ComP-ComA, LiaS-LiaR, DesR-DesK TCSs, respectively. Proteins having this HATPase domain have a histidine kinase dimerization and phosphoacceptor domain; some have accessory domains such as GAF, HAMP, PAS and MASE sensor domains.	7.41187e-11
NZ_LS483523.1\|WP_016397473.1\|1535586_1537602_-\|ABC-transporter-permease	gnl\|CDD\|226957	COG4591, LolE, ABC-type transport system, involved in lipoprotein release, permease component [Cell envelope biogenesis, outer membrane].	0.000223641

>NZ_LS483523.1|WP_023396274.1|1546847_1547258_-|hypothetical-protein
METIYQRDSDQDGLTDAQELALGTNPLSADSDGDGRSDLVEVEEGSNPLEKDFQDIDQTSITEPSSVFMEMKQKISDMMESHHKEFIQVLISIETGIENEQDLEDLYTYYMRTDAVSLLSSDLETSPQEVEMEIEL
>NZ_LS483523.1|WP_023396275.1|1540217_1540502_-|hypothetical-protein
MMEDTYYQLEEALVQGFQTPEEYNAYKELKEHYEEVTGDYSFSKRELTSQLEISLQNHRGVDFEEHEKEEYLDLVQKLEEFDSSLATHYRQLID
>NZ_LS483523.1|WP_075575678.1|1539904_1540225_-|hypothetical-protein
MTRKEKVMNDLLLIPVIFLAVGGILILLWRLFLIASGLFLIGFVSFLIFIEVYGIYLFFTEPTLYIEDLSQNGLISFTGFYVVFNLALLVCGVLKIISWTRRLKSS
>NZ_LS483523.1|WP_023396277.1|1539567_1539750_-|hypothetical-protein
MSKNTSRPEIDSLSFEVENQELSGKSGSGWFTAVQLTLAGRCGRWFTGSFECTTNNVKCG
>NZ_LS483523.1|WP_016397470.1|1539227_1539410_-|hypothetical-protein
MRKNNNHKEIDTLDFEVKNQELSGKSGSGWFTAVQLTLAGRCGRWFTGSYECTSNNVKCG
>NZ_LS483523.1|WP_023396278.1|1538882_1539065_-|hypothetical-protein
MKSKKVNTEIDTLEFEIDNQELNGTSGSGWWYTAFKMTLAGRCGLCFTCSYECTTNNVRC
>NZ_LS483523.1|WP_025172692.1|1538619_1538796_-|hypothetical-protein
MKQDNFEIDSLDYEINSQELNGKSAAGWRTAVRLTVQGRCGWWFTYSYECTSPNVRCG
>NZ_LS483523.1|WP_023396803.1|1537614_1538349_-|ABC-transporter-ATP-binding-protein
MKQLIVTGLTKIFGQGDNIVHALLDVNLSVEKGEFLAIMGASGSGKTTLLNCISTIDKPTSGEIRFEDFDIIHAKENELADYRAKNISYIFQAYNLVETLTVYENIVLPLQIQGKNIKKHQDKIEEILDKLAIQNLKDKFPNQLSGGQRQRVATARALIDDSKLIIADEPTGALDSANSEKLMALLQEINKSFGITILLVTHDPAAAKYSSRMVLLSDGKIMDDLERNSLSNEQYLQEIYSRAR
>NZ_LS483523.1|WP_016397473.1|1535586_1537602_-|ABC-transporter-permease
MYPKLILRNVFRNLQTYTIYFFSLTLIYSLLYAFNALPSHPVMQSLSGAKEMLTTVMSQYMGLLSYLILSAIAFLVVYSTNFVLGRRKKELGLYATLGMKKKQIIRTLFFETMLVNIFSLILGFLLGVILLVILAKIASEFFMANYFGSLLFFDSKSVILLVYSYLVTSFIVGVMDILTFRKQNIIALIQENGVKKSVLAKGKPALQALLFILSTAVIGFGALYFSDYHHLSLLKSWGILLVSVFVIFVILFYNTLSHFILVSLRKLPQTYYNKLNSFKIRQFSKQADSNSVTLAVLSLTLTLALSLLVFSGSAYTTMNRELNKYSPYDVSVNLYRGQEFQFSQESVKDRLKADGFDFNLIKEEYSYPIYSSDLTYKDLIDTSNLWAHDKELPESKVPILGISAYNHLRKLQGKKAVDLADNQFLVNANYKGTAKQIQDFLLTTKTLMINGYSLNLASSKPLETVYFLSSVGTNDTGTLIVPDTVVVGLMEDHTTYVANFKENIDKRKVETFLSQWIEKYYFTRDGAELNPFTYQTKGRIFEIYLGFMGVIVFVMIFVSVIFIIISLSILSLQTSTSSLDSVNDYQILYLLGNKRKQNRSILLQQILSYFLVPLVIAGPLALALSTALLGYFENFANTSISIDITYLGVAVLLFVLYLLVTYRVSWQIIEN
>NZ_LS483523.1|WP_016397474.1|1533931_1535506_-|ATP-binding-protein
MKQFVKLISKNSLLLWWLTIFNHLTLMIYIYYRIPLDFSTDFSLQMVLLLIIALIAFSYICNIVTFRYSELKLWLLLMMFLISWQSIFNQGVTSTLLHFFDILHPLNYFLLVYSSLSILFLGEKIGEELLSVSFVLTLITVSSYLLSPSIFLFLSLFASFFLNLVPLILFILYHEELKSKLKYQRRNLWILALILPLSYFFLYINTTGSGVMNLVWYLEILGILAFLHFKTIVSSLQKKVSELKLSYIKAFSRLFLLVMFLLVGIFIIFRLDLNTSFLVLNIMLLLFGICSEELIRLFRSAEMLDSRDYVKVLFLKRNRMVKNLLANEDTEQQFSEFLHNEILQNVMAIKNFNKYSSNQAFGEQINLVTEELVQRIRERMDYYQPMIETDEQLDIQYQGLINRIVKRYHAENEVVTQFPVHFRLLSPYDKIAYRLVEELTTNAVKYASGGTISLKIDVHDDAIFIISENDCLQIEKSLGYGLKNMSNKISVLGGQMQIFENNKRFRVEITLPIDKELCYENFVN
>NZ_LS483523.1|WP_023396273.1|1547720_1547885_+|hypothetical-protein
MATISLTRDIKLTNEDALKILNHKPSKKLQAVLKSIESQNATAPTKNKLISKYL
>NZ_LS483523.1|WP_023396270.1|1548529_1551343_-|CHAP-domain-containing-protein
MKDKREIIRARKAFRRSLKDEKKFLKQGKKEVRKQKKDSAVLDENAWKKEIKEKLEEMREASKAKVKQANEDYNHILQNSPPSLLNRKELRDRRLPHARKRLKIAKKQFKEAKVEAKSERKESRKERKTNQKFLYGQESKAKSNFFFHGKNLEELKAKKEVKVAKENLKSTKQAYKSKKVSRKAKTFLYVLGREGGELASENEDLEGYRTLQETIRKGKRYSRLSYNLGKASVKTGQATGRFTKKRLTNTKERYHHFKDGKGWKLAKENPSSFKNRFRKLKKQGLTSVRNIYQKLKAAFSFFTFAAGNPATWIVGGLVFLLLLMMSFFLGFSSASLIQQDEFELTKAYTHLTWEDAEHTRTNDKGITYYTKVDDVMGYMNFKFHDYELHKPVYLFSSETYKDYLSTLWHDLNDGDDLKSMQDLYETPKYKLSKDDQEEIKELKEEGVYASMQELDNPFEGQSNEDSLTMTYRYGYYDLDGKPTLQEYILLEAKAHQTIVAPMDGVVSLDGDNIILTNGKGENESRLTLHSIHNGRAIEGTRVLTGDVIGETPDDTGLKVSYQKYKNKKEKLVYVNPQFYFPKVIQLQTTILPAIGQFGGDEFERAKHIYEFLKSQGASPQAIAAILENWSVESSINPKRAEGDYLFPPVGATDSSWDDETWLAIGGPAIYSGAYPNILHRGLGLGQWTDTADGSTRHTALLNYAHAKNKKWYDLDLQLDFMLHGDSPYYQSWLKDFFGNTGSAANLAQLFLTYWEGNSGDKLLERQTRATEWYYQIEKGFSQTNGGQAKSDPQSLEGVRGDLYDHSVPGGGDGMAYAYGQCTWGVAARMNQLGLKLKGSNGEKISIINTMGNGQDWVATASSLGGETGSIPRAGAIVSFVGGTHGTPADYGHVAFVEKVYDDGSFLVSETNYGGNPNYTFRKISQADSAISFAYTTK
>NZ_LS483523.1|WP_000824174.1|1551354_1553712_-|hypothetical-protein
MKRKSNTLKKQKTSMTNKKEVVKGKKEEVLPSTANTLYYQALYQNGLMQVKEDYFSQSYLLGDVNYQTVGLEDKGAIIEKYSDLINSLDDQTNFQLTIFNKRLNLEKFRQSVLYEEKEDGYDSYRKELNRMMNQNLDSGENNFSAVKLITFGRKDSNPKQAYRSLSQIGEYFKSGFSEIDARFESLAGENRVNLLADMLRGEHHLPFSYRDLTRSGQTTRHFIAPNLLDFKNKNYLQINDRLLQIVYVRDYGMELGDQFIRDLMQGDLELIVSLHAQSSTKADAMKKLRTKKTLMESQKIGEQQKLARTGIYLEKVGHVLESNIDEAEELLKTMTETGDKLFQTVFLIGVFGQDEEELKQALDTIQQVAGSNDLMIDKLPYMQEAAFNSLLPFGCDFLEGVSRSLLTSNVAVNSPWTSVDLQDRSGKYYGINQISSNIITIDRSLLNTPSGLILGTSGAGKGMATKHEIITTKIKESGENTEIIIVDPEAEYSVIGRAFGGEMIDIAPDSQTYLNVLDLSEENMDEDPVKVKSEFLLSFIGKLLDRKMDGREKSIIDRVTRLTYQSFKEPSLEEWVFVLSQQPEEEAQNLALDMELYVEGSLDIFSHKTNIQTGSNFLIYNVKKLGDELKQIALMVVFDQIWNRVVRNQKLGKKTWIYFDEMQLLLLDKYASDFFFKLWSRVRKYGASPTGITQNVETLLLDPNGRRIIANSEFMILLKQAKNDREELVQLLGLSKELEKYLVNPEKGAGLIKAGSVVVPFKNKIPQGTQLFDIMSTDPDKMASN
>NZ_LS483523.1|WP_001097589.1|1553662_1554022_-|PrgI-family-protein
MNTRVFKDISKYQHRAWLGFTTRQIIFVLPAFIVTIIVLGLNLFFWQFGDWFVYGFVFAFTIPLMLFGVYKPNDLYFEHYLKYRLHFELTVPLRTITGKKGPEHEKKIKYIKETKNFND
>NZ_LS483523.1|WP_001054257.1|1554075_1554930_-|conjugal-transfer-protein-TrbL
MNLSLVSPFVYLASEKISAENLFEGFNVDLQSTVDLIKSLSSYNPTVWTYMSSITKSVMQPLGVAILSVVLILEFSKMAKKIANSGGAMTFEALAPMLISYIMVAVVITNTTVIVEAIIGIASHAIEQVASIVAHGGAKYDTISGLKGSGFIGRMIVGFFALLIWLVRIVSAAMVNLLVSIRFIQLYLMIPFAPLTIPTFLSDEWKSIGIGYLKNIMVYAVQGVLIFLIVSLVPLFESAGKIAVSNGAGVLQSLAIMFGSLVQAILLIIALVGSQRTARSILGM
>NZ_LS483523.1|WP_000627868.1|1554946_1555189_-|hypothetical-protein
MITHFKGLVYGVDASAMFAQAMSLLQKGLIAVGAFLVVVGIVNLATNIKDGGPGVRNAILEIVGGVMVGAAGAFVTQISI
>NZ_LS483523.1|WP_023396268.1|1555958_1556768_-|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein
MFSNANSFKAKIKNISKDKGIPAQQVQQHYLIEQVLKLISTSSYRDSFIVKGGYLIGQMIGLDKRTTMDLDVTLKGTEMSRENLIDIFEEILCSKTDGFSFSVDKLEPIRQDDEYGGFSLKLNATFDTLKEVVFIDITTGDKITPREITYSMTSIFTNESIKIWTYNLETVLAEKLETIISRGLASTRPRDRYDLFTLYKLRKEEINLEVLKNALENTAKKRKSKDTIYNWEEQVRGIEISDYQKELWIRYQRQFKYAKDISLFKVSWT
>NZ_LS483523.1|WP_000227921.1|1556767_1557358_-|type-IV-toxin-antitoxin-system-AbiEi-family-antitoxin-domain-containing-protein
MVDKREKLMNSFNQYGFLTFKQVIDENLHYKTLLKMVTEGKIDAEEKGLYRLPDIYLDEWFVIQYRFPKGIFSLETALWLHGLSLTIPFNMTMSFPYGTNTKNIKEADICPIILRSHYSEGIIEIERLPGQFIKVYEIERVLVECLRPVHQVDLQIIAPAFKKYFQQNQIHLHKLFYYAQLFKVTDKLQSYTEVLS
>NZ_LS483523.1|WP_000821278.1|1557487_1558075_-|CPBP-family-intramembrane-metalloprotease
MKRIIPVYIFQQVNVLLVSLYLLKFLCIGELTILQILYGASLISFLWMYGQRKQAHKVNMKSRIKWLGIGFVSLLIISLCFSLIHAQGSTNQANLIGLQHQVPWFSFLLFLINASMVEEFLYREILWNLVRKLDIRVALTCVLFALAHHPGTILAWCLYVSLGLFLGMVRYKSDLWGSMGLHLVWNLSVYVLFFL
>NZ_LS483523.1|WP_000840778.1|1558077_1558311_-|hypothetical-protein
MAERFWENLSIILAERNISWIELTRKMFAGEFHYPSELNRLYQKIRHYKVEQRMPQSPWVERIVQVLDLDYEDLFRR

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_LS483523_3	3.90\|981400\|30\|NZ_LS483523\|CRT	981400-981429	30	NZ_CP046029	Staphylococcus chromogenes strain 1401 plasmid unnamed1	25145-25174	3	0.9
NZ_LS483523_3	3.106\|982216\|30\|NZ_LS483523\|CRT	982216-982245	30	NZ_CP046029	Staphylococcus chromogenes strain 1401 plasmid unnamed1	25145-25174	3	0.9
NZ_LS483523_3	3.302\|975514\|30\|NZ_LS483523\|CRT	975514-975543	30	NZ_CP046029	Staphylococcus chromogenes strain 1401 plasmid unnamed1	25145-25174	3	0.9
NZ_LS483523_3	3.331\|976984\|30\|NZ_LS483523\|CRT	976984-977013	30	NZ_CP046029	Staphylococcus chromogenes strain 1401 plasmid unnamed1	25145-25174	3	0.9
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	NZ_CP018759	Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence	53916-53945	4	0.867
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	NZ_CP018759	Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence	53913-53942	5	0.833
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NC_007766	Rhizobium etli CFN 42 plasmid p42f, complete sequence	592340-592369	5	0.833
NZ_LS483523_3	3.256\|985816\|30\|NZ_LS483523\|CRT	985816-985845	30	MK494091	Mycobacterium phage Scorpia, complete genome	43487-43516	5	0.833
NZ_LS483523_3	3.256\|985816\|30\|NZ_LS483523\|CRT	985816-985845	30	JN083853	Mycobacterium phage Airmid, complete genome	43654-43683	5	0.833
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	167409-167438	5	0.833
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	759452-759481	5	0.833
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	939046-939075	5	0.833
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	NZ_CP018759	Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence	53913-53942	5	0.833
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NC_007766	Rhizobium etli CFN 42 plasmid p42f, complete sequence	592340-592369	5	0.833
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP051294	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence	29162-29191	5	0.833
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP033363	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence	29162-29191	5	0.833
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	694695-694724	5	0.833
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	158192-158221	5	0.833
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	76414-76443	5	0.833
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	13077-13106	5	0.833
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	163628-163657	5	0.833
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	MG592531	Vibrio phage 1.164.O._10N.261.51.A7, partial genome	8617-8646	6	0.8
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	MG592541	Vibrio phage 1.174.O._10N.261.55.A8, partial genome	8498-8527	6	0.8
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP028970	Aminobacter sp. MSH1 plasmid pUSP2, complete sequence	359835-359864	6	0.8
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	MG592531	Vibrio phage 1.164.O._10N.261.51.A7, partial genome	8617-8646	6	0.8
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	MG592541	Vibrio phage 1.174.O._10N.261.55.A8, partial genome	8498-8527	6	0.8
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP028970	Aminobacter sp. MSH1 plasmid pUSP2, complete sequence	359835-359864	6	0.8
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	CP000621	Burkholderia vietnamiensis G4 plasmid pBVIE05, complete sequence	45744-45773	6	0.8
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	MT701594	Streptomyces phage Spernnie, complete genome	42471-42500	6	0.8
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NC_007766	Rhizobium etli CFN 42 plasmid p42f, complete sequence	592343-592372	6	0.8
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1655094-1655123	6	0.8
NZ_LS483523_3	3.42\|978478\|30\|NZ_LS483523\|CRT	978478-978507	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP013503	Rhizobium esperanzae strain N561 plasmid pRspN561c, complete sequence	150034-150063	7	0.767
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP013509	Rhizobium sp. N1341 plasmid pRspN1341d, complete sequence	150034-150063	7	0.767
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP013520	Rhizobium sp. N113 plasmid pRspN113c, complete sequence	150034-150063	7	0.767
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP013493	Rhizobium sp. N6212 plasmid pRspN6212c, complete sequence	150034-150063	7	0.767
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP013516	Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence	147694-147723	7	0.767
NZ_LS483523_3	3.58\|979168\|30\|NZ_LS483523\|CRT	979168-979197	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.89\|981352\|30\|NZ_LS483523\|CRT	981352-981381	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.90\|981400\|30\|NZ_LS483523\|CRT	981400-981429	30	NC_010553	Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence	40970-40999	7	0.767
NZ_LS483523_3	3.92\|981484\|30\|NZ_LS483523\|CRT	981484-981513	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.106\|982216\|30\|NZ_LS483523\|CRT	982216-982245	30	NC_010553	Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence	40970-40999	7	0.767
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	AP014939	Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243	77738-77767	7	0.767
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	NZ_LN681228	Xenorhabdus nematophila AN6/1 plasmid II, complete sequence	41775-41804	7	0.767
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	NZ_AP018687	Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence	109927-109956	7	0.767
NZ_LS483523_3	3.111\|982420\|30\|NZ_LS483523\|CRT	982420-982449	30	MT701594	Streptomyces phage Spernnie, complete genome	42474-42503	7	0.767
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP027671	Simplicispira suum strain SC1-8 plasmid unnamed2, complete sequence	56588-56617	7	0.767
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP024314	Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence	2014639-2014668	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	NC_015065	Granulicella tundricola MP5ACTX9 plasmid pACIX902, complete sequence	154358-154387	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	AP013475	Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C83-MedDCM-OCT-S45-C54	29951-29980	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	NC_034248	Rhizobium phage RHEph10, complete genome	46444-46473	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	MN096365	Gordonia phage Samba, complete genome	30298-30327	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	MT639640	Gordonia phage Paries, complete genome	21871-21900	7	0.767
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	MK977702	Gordonia terrae phage McKinley, complete genome	22215-22244	7	0.767
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	JN106170	Uncultured bacterium plasmid pAKD25, complete sequence	30821-30850	7	0.767
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	JN106175	Uncultured bacterium plasmid pAKD34, complete sequence	30820-30849	7	0.767
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	JN106167	Uncultured bacterium plasmid pAKD16, complete sequence	41228-41257	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	MK759884	Salmonella phage vB_SenM_SB18, complete genome	25544-25573	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	NC_015292	Erwinia phage phiEa104, complete genome	25562-25591	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	MH426725	Erwinia phage SunLIRen, complete genome	25548-25577	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	FQ482083	Erwinia amylovora phage phiEa104 complete genome	25562-25591	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	NC_011811	Erwinia phage phiEa21-4, complete genome	25571-25600	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	MG589384	Enterobacter phage phi63_307, complete genome	68679-68708	7	0.767
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	MK770412	Salmonella phage SE5, complete genome	55742-55771	7	0.767
NZ_LS483523_3	3.284\|974722\|30\|NZ_LS483523\|CRT	974722-974751	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.290\|975046\|30\|NZ_LS483523\|CRT	975046-975075	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.302\|975514\|30\|NZ_LS483523\|CRT	975514-975543	30	NC_010553	Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence	40970-40999	7	0.767
NZ_LS483523_3	3.303\|975562\|30\|NZ_LS483523\|CRT	975562-975591	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.305\|975682\|30\|NZ_LS483523\|CRT	975682-975711	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.315\|976270\|30\|NZ_LS483523\|CRT	976270-976299	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.317\|976360\|30\|NZ_LS483523\|CRT	976360-976389	30	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	443146-443175	7	0.767
NZ_LS483523_3	3.331\|976984\|30\|NZ_LS483523\|CRT	976984-977013	30	NC_010553	Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence	40970-40999	7	0.767
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	AP014939	Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243	77738-77767	7	0.767
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	NZ_LN681228	Xenorhabdus nematophila AN6/1 plasmid II, complete sequence	41775-41804	7	0.767
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	NZ_AP018687	Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence	109927-109956	7	0.767
NZ_LS483523_3	3.336\|977188\|30\|NZ_LS483523\|CRT	977188-977217	30	MT701594	Streptomyces phage Spernnie, complete genome	42474-42503	7	0.767
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP027671	Simplicispira suum strain SC1-8 plasmid unnamed2, complete sequence	56588-56617	7	0.767
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP024314	Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence	2014639-2014668	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	NC_015065	Granulicella tundricola MP5ACTX9 plasmid pACIX902, complete sequence	154358-154387	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	AP013475	Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C83-MedDCM-OCT-S45-C54	29951-29980	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	NC_034248	Rhizobium phage RHEph10, complete genome	46444-46473	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	MN096365	Gordonia phage Samba, complete genome	30298-30327	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	MT639640	Gordonia phage Paries, complete genome	21871-21900	7	0.767
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	MK977702	Gordonia terrae phage McKinley, complete genome	22215-22244	7	0.767
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	AP014939	Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243	77735-77764	7	0.767
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	NZ_LN681228	Xenorhabdus nematophila AN6/1 plasmid II, complete sequence	41772-41801	7	0.767
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	NZ_AP018687	Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence	109930-109959	7	0.767
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	MG592531	Vibrio phage 1.164.O._10N.261.51.A7, partial genome	8614-8643	7	0.767
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	MG592541	Vibrio phage 1.174.O._10N.261.55.A8, partial genome	8495-8524	7	0.767
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP016722	Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence	8166-8195	7	0.767
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NC_004444	Pseudomonas resinovorans plasmid pCAR1, complete sequence	15836-15865	7	0.767
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NC_021506	Pseudomonas resinovorans NBRC 106553 plasmid pCAR1.3, complete sequence	15836-15865	7	0.767
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NC_011838	Pseudomonas putida plasmid pCAR1.2, complete sequence	15836-15865	7	0.767
NZ_LS483523_3	3.390\|983983\|30\|NZ_LS483523\|CRT	983983-984012	30	MN224564	Streptomyces phage Araceli, complete genome	10865-10894	7	0.767
NZ_LS483523_3	3.390\|983983\|30\|NZ_LS483523\|CRT	983983-984012	30	MH697589	Microbacterium phage Neferthena, complete genome	21739-21768	7	0.767
NZ_LS483523_3	3.390\|983983\|30\|NZ_LS483523\|CRT	983983-984012	30	MH229863	Streptomyces phage JackieB, complete genome	10730-10759	7	0.767
NZ_LS483523_3	3.390\|983983\|30\|NZ_LS483523\|CRT	983983-984012	30	MH229862	Streptomyces phage Henoccus, complete genome	10875-10904	7	0.767
NZ_LS483523_3	3.394\|984139\|30\|NZ_LS483523\|CRT	984139-984168	30	NZ_CP049158	Caballeronia sp. SBC1 plasmid pSBC1_2, complete sequence	140298-140327	7	0.767
NZ_LS483523_3	3.394\|984139\|30\|NZ_LS483523\|CRT	984139-984168	30	NZ_CP049318	Caballeronia sp. SBC2 plasmid pSBC2-2, complete sequence	140245-140274	7	0.767
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	MF580956	Salinibacter virus M8CC-19, complete genome	40494-40523	7	0.767
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	MF580959	Salinibacter virus M8CRM-1, partial genome	40138-40167	7	0.767
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	MF580960	Salinibacter virus M31CC-1, partial genome	40491-40520	7	0.767
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	1025510-1025539	7	0.767
NZ_LS483523_3	3.395\|984187\|30\|NZ_LS483523\|CRT	984187-984216	30	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	1726303-1726332	7	0.767
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP016722	Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence	8163-8192	8	0.733
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP027023	Streptomyces sp. WAC00288 plasmid p1, complete sequence	176839-176868	8	0.733
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1655097-1655126	8	0.733
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP051294	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence	29165-29194	8	0.733
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP033363	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence	29165-29194	8	0.733
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	LR134127	Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7	196465-196494	8	0.733
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	MN693854	Marine virus AFVG_250M929, complete genome	19997-20026	8	0.733
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	MN694256	Marine virus AFVG_250M930, complete genome	19852-19881	8	0.733
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	NZ_LR594668	Variovorax sp. SRS16 plasmid 3	451342-451371	8	0.733
NZ_LS483523_3	3.116\|982624\|30\|NZ_LS483523\|CRT	982624-982653	30	NZ_CP016617	Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence	935570-935599	8	0.733
NZ_LS483523_3	3.256\|985816\|30\|NZ_LS483523\|CRT	985816-985845	30	NZ_LN831184	Vibrio cholerae isolate V. cholerae 116-14 plasmid pNDM-116-14, complete sequence	137681-137710	8	0.733
NZ_LS483523_3	3.256\|985816\|30\|NZ_LS483523\|CRT	985816-985845	30	MN586060	Mycobacterium phage PetterN, complete genome	43916-43945	8	0.733
NZ_LS483523_3	3.256\|985816\|30\|NZ_LS483523\|CRT	985816-985845	30	KT246486	Mycobacterium phage Chadwick, complete genome	43130-43159	8	0.733
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	MT227925	Vibrio phage phiV141, complete genome	16029-16058	8	0.733
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	MN582094	Siphoviridae sp. ctjeG17, complete genome	53994-54023	8	0.733
NZ_LS483523_3	3.258\|985900\|30\|NZ_LS483523\|CRT	985900-985929	30	HQ633071	Synechococcus phage S-SKS1 genomic sequence	168395-168424	8	0.733
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	MH179480	Pseudomonas phage 98PfluR60PP, complete genome	40891-40920	8	0.733
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP016722	Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence	8163-8192	8	0.733
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP027023	Streptomyces sp. WAC00288 plasmid p1, complete sequence	176839-176868	8	0.733
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1655097-1655126	8	0.733
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP051294	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence	29165-29194	8	0.733
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP033363	Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence	29165-29194	8	0.733
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	LR134127	Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7	196465-196494	8	0.733
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	MN693854	Marine virus AFVG_250M929, complete genome	19997-20026	8	0.733
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	MN694256	Marine virus AFVG_250M930, complete genome	19852-19881	8	0.733
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	NZ_LR594668	Variovorax sp. SRS16 plasmid 3	451342-451371	8	0.733
NZ_LS483523_3	3.341\|977392\|30\|NZ_LS483523\|CRT	977392-977421	30	NZ_CP016617	Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence	935570-935599	8	0.733
NZ_LS483523_3	3.381\|983635\|30\|NZ_LS483523\|CRT	983635-983664	30	MH220877	Oenococcus phage phiOE33PA, complete genome	7687-7716	8	0.733
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP027023	Streptomyces sp. WAC00288 plasmid p1, complete sequence	176836-176865	8	0.733
NZ_LS483523_3	3.390\|983983\|30\|NZ_LS483523\|CRT	983983-984012	30	CP003186	Thermoanaerobacterium phage THSA-485A, complete genome	9218-9247	8	0.733
NZ_LS483523_3	3.55\|979030\|30\|NZ_LS483523\|CRT	979030-979059	30	NZ_CP015739	Shinella sp. HZN7 plasmid pShin-03, complete sequence	386468-386497	9	0.7
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP049701	Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence	5793-5822	9	0.7
NZ_LS483523_3	3.112\|982468\|30\|NZ_LS483523\|CRT	982468-982497	30	NZ_CP049701	Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence	300706-300735	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	NC_049494	Acinetobacter phage vB_AbaM_PhT2, complete genome	5726-5755	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013499	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S39-C84	5459-5488	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013497	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S35-C79	21583-21612	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013498	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S38-C76	7232-7261	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013776	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C68A-MedDCM-OCT-S36-C73, * SEQUENCING IN PROGRESS *	3859-3888	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013496	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S28-C61	9185-9214	9	0.7
NZ_LS483523_3	3.264\|986128\|30\|NZ_LS483523\|CRT	986128-986157	30	AP013775	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C68A-MedDCM-OCT-S26-C73, * SEQUENCING IN PROGRESS *	26208-26237	9	0.7
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP049701	Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence	5793-5822	9	0.7
NZ_LS483523_3	3.337\|977236\|30\|NZ_LS483523\|CRT	977236-977265	30	NZ_CP049701	Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence	300706-300735	9	0.7
NZ_LS483523_3	3.383\|983719\|30\|NZ_LS483523\|CRT	983719-983748	30	NZ_CP028970	Aminobacter sp. MSH1 plasmid pUSP2, complete sequence	359832-359861	9	0.7
NZ_LS483523_3	3.90\|981400\|30\|NZ_LS483523\|CRT	981400-981429	30	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	167415-167444	13	0.567
NZ_LS483523_3	3.90\|981400\|30\|NZ_LS483523\|CRT	981400-981429	30	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	759458-759487	13	0.567
NZ_LS483523_3	3.90\|981400\|30\|NZ_LS483523\|CRT	981400-981429	30	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	939052-939081	13	0.567
NZ_LS483523_3	3.106\|982216\|30\|NZ_LS483523\|CRT	982216-982245	30	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	167415-167444	13	0.567
NZ_LS483523_3	3.106\|982216\|30\|NZ_LS483523\|CRT	982216-982245	30	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	759458-759487	13	0.567
NZ_LS483523_3	3.106\|982216\|30\|NZ_LS483523\|CRT	982216-982245	30	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	939052-939081	13	0.567
NZ_LS483523_3	3.302\|975514\|30\|NZ_LS483523\|CRT	975514-975543	30	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	167415-167444	13	0.567
NZ_LS483523_3	3.302\|975514\|30\|NZ_LS483523\|CRT	975514-975543	30	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	759458-759487	13	0.567
NZ_LS483523_3	3.302\|975514\|30\|NZ_LS483523\|CRT	975514-975543	30	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	939052-939081	13	0.567
NZ_LS483523_3	3.331\|976984\|30\|NZ_LS483523\|CRT	976984-977013	30	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	167415-167444	13	0.567
NZ_LS483523_3	3.331\|976984\|30\|NZ_LS483523\|CRT	976984-977013	30	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	759458-759487	13	0.567
NZ_LS483523_3	3.331\|976984\|30\|NZ_LS483523\|CRT	976984-977013	30	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	939052-939081	13	0.567

1. spacer 3.90|981400|30|NZ_LS483523|CRT matches to NZ_CP046029 (Staphylococcus chromogenes strain 1401 plasmid unnamed1) position: , mismatch: 3, identity: 0.9

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agcgcaagtacgtcattaagcacgtcagta	Protospacer
*************** .***********.*

2. spacer 3.106|982216|30|NZ_LS483523|CRT matches to NZ_CP046029 (Staphylococcus chromogenes strain 1401 plasmid unnamed1) position: , mismatch: 3, identity: 0.9

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agcgcaagtacgtcattaagcacgtcagta	Protospacer
*************** .***********.*

3. spacer 3.302|975514|30|NZ_LS483523|CRT matches to NZ_CP046029 (Staphylococcus chromogenes strain 1401 plasmid unnamed1) position: , mismatch: 3, identity: 0.9

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agcgcaagtacgtcattaagcacgtcagta	Protospacer
*************** .***********.*

4. spacer 3.331|976984|30|NZ_LS483523|CRT matches to NZ_CP046029 (Staphylococcus chromogenes strain 1401 plasmid unnamed1) position: , mismatch: 3, identity: 0.9

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agcgcaagtacgtcattaagcacgtcagta	Protospacer
*************** .***********.*

5. spacer 3.381|983635|30|NZ_LS483523|CRT matches to NZ_CP018759 (Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence) position: , mismatch: 4, identity: 0.867

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gcaagaaggtccgcatcaacaagcgcgtgt	Protospacer
***** * ******************. **

6. spacer 3.111|982420|30|NZ_LS483523|CRT matches to NZ_CP018759 (Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence) position: , mismatch: 5, identity: 0.833

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
agggcaagaaggtccgcatcaacaagcgcg	Protospacer
  ****** * ******************.

7. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NC_007766 (Rhizobium etli CFN 42 plasmid p42f, complete sequence) position: , mismatch: 5, identity: 0.833

tcggcat-caacaagcgcgtcgacctcagca	CRISPR spacer
-cgacctgcaacaagcgggtcgaactcagca	Protospacer
 **.* * ********* ***** *******

8. spacer 3.256|985816|30|NZ_LS483523|CRT matches to MK494091 (Mycobacterium phage Scorpia, complete genome) position: , mismatch: 5, identity: 0.833

tcgacc-tcagcaagcacgtcagcaagtaca	CRISPR spacer
-cgcccgtcagccaacacgtcagcaagtacg	Protospacer
 ** ** ***** *.***************.

9. spacer 3.256|985816|30|NZ_LS483523|CRT matches to JN083853 (Mycobacterium phage Airmid, complete genome) position: , mismatch: 5, identity: 0.833

tcgacc-tcagcaagcacgtcagcaagtaca	CRISPR spacer
-cgtccgtcagccaacacgtcagcaagtacg	Protospacer
 ** ** ***** *.***************.

10. spacer 3.258|985900|30|NZ_LS483523|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 5, identity: 0.833

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
acgccgtcggcaagcacgtcagcaagcacg	Protospacer
*   ****.********.************

11. spacer 3.258|985900|30|NZ_LS483523|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
acgccgtcggcaagcacgtcagcaagcacg	Protospacer
*   ****.********.************

12. spacer 3.258|985900|30|NZ_LS483523|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.833

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
acgccgtcggcaagcacgtcagcaagcacg	Protospacer
*   ****.********.************

13. spacer 3.336|977188|30|NZ_LS483523|CRT matches to NZ_CP018759 (Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence) position: , mismatch: 5, identity: 0.833

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
agggcaagaaggtccgcatcaacaagcgcg	Protospacer
  ****** * ******************.

14. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NC_007766 (Rhizobium etli CFN 42 plasmid p42f, complete sequence) position: , mismatch: 5, identity: 0.833

tcggcat-caacaagcgcgtcgacctcagca	CRISPR spacer
-cgacctgcaacaagcgggtcgaactcagca	Protospacer
 **.* * ********* ***** *******

15. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP051294 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence) position: , mismatch: 5, identity: 0.833

gcatcaacaagcgcgtcgacctca-gcaagc	CRISPR spacer
acatcaacaagggcttcgacctcatgcatg-	Protospacer
.********** ** ********* *** *

16. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP033363 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence) position: , mismatch: 5, identity: 0.833

gcatcaacaagcgcgtcgacctca-gcaagc	CRISPR spacer
acatcaacaagggcttcgacctcatgcatg-	Protospacer
.********** ** ********* *** *

17. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 5, identity: 0.833

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagttcatcggcaactacgtccacgaca	Protospacer
****** ********* *******.*. **

18. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.833

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagttcatcggcaactacgtccacgaca	Protospacer
****** ********* *******.*. **

19. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 5, identity: 0.833

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagttcatcggcaattacgtccacgaca	Protospacer
****** ********* *******.*. **

20. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.833

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagttcatcggcaactacgtccacgaca	Protospacer
****** ********* *******.*. **

21. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.833

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagttcatcggcaattacgtccacgaca	Protospacer
****** ********* *******.*. **

22. spacer 3.111|982420|30|NZ_LS483523|CRT matches to MG592531 (Vibrio phage 1.164.O._10N.261.51.A7, partial genome) position: , mismatch: 6, identity: 0.8

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
tttgctggtacgtctgcatcaccaagcgca	Protospacer
*. ** .*******.****** ********

23. spacer 3.111|982420|30|NZ_LS483523|CRT matches to MG592541 (Vibrio phage 1.174.O._10N.261.55.A8, partial genome) position: , mismatch: 6, identity: 0.8

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
tttgctggtacgtctgcatcatcaagcgca	Protospacer
*. ** .*******.****** ********

24. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP028970 (Aminobacter sp. MSH1 plasmid pUSP2, complete sequence) position: , mismatch: 6, identity: 0.8

tcggca-tcaacaagcgcgtcgacctcagca	CRISPR spacer
-agacaggcaacaagggcgtcgacctcatca	Protospacer
  *.**  ******* ************ **

25. spacer 3.336|977188|30|NZ_LS483523|CRT matches to MG592531 (Vibrio phage 1.164.O._10N.261.51.A7, partial genome) position: , mismatch: 6, identity: 0.8

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
tttgctggtacgtctgcatcaccaagcgca	Protospacer
*. ** .*******.****** ********

26. spacer 3.336|977188|30|NZ_LS483523|CRT matches to MG592541 (Vibrio phage 1.174.O._10N.261.55.A8, partial genome) position: , mismatch: 6, identity: 0.8

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
tttgctggtacgtctgcatcatcaagcgca	Protospacer
*. ** .*******.****** ********

27. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP028970 (Aminobacter sp. MSH1 plasmid pUSP2, complete sequence) position: , mismatch: 6, identity: 0.8

tcggca-tcaacaagcgcgtcgacctcagca	CRISPR spacer
-agacaggcaacaagggcgtcgacctcatca	Protospacer
  *.**  ******* ************ **

28. spacer 3.381|983635|30|NZ_LS483523|CRT matches to CP000621 (Burkholderia vietnamiensis G4 plasmid pBVIE05, complete sequence) position: , mismatch: 6, identity: 0.8

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gtaagaaagtccgcatcaacaagcggattt	Protospacer
*.*** * ***************** *  *

29. spacer 3.381|983635|30|NZ_LS483523|CRT matches to MT701594 (Streptomyces phage Spernnie, complete genome) position: , mismatch: 6, identity: 0.8

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gcaagcacgtccgcaacaacaagtacgagg	Protospacer
*****.********* *******..*.**

30. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NC_007766 (Rhizobium etli CFN 42 plasmid p42f, complete sequence) position: , mismatch: 6, identity: 0.8

gcatcaacaagcgcgtcgacctcagcaagc	CRISPR spacer
cctgcaacaagcgggtcgaactcagcaaga	Protospacer
 *  ********* ***** *********

31. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.8

gcatcaacaagcgcgtcgacctca-gcaagc	CRISPR spacer
acatcaacaagggcttcgacctcatgcaca-	Protospacer
.********** ** ********* *** .

32. spacer 3.42|978478|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

33. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP013503 (Rhizobium esperanzae strain N561 plasmid pRspN561c, complete sequence) position: , mismatch: 7, identity: 0.767

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
aggaaggccgcgtcggcttcagcatcgaca	Protospacer
** *  . .**************.******

34. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP013509 (Rhizobium sp. N1341 plasmid pRspN1341d, complete sequence) position: , mismatch: 7, identity: 0.767

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
aggaaggccgcgtcggcttcagcatcgaca	Protospacer
** *  . .**************.******

35. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP013520 (Rhizobium sp. N113 plasmid pRspN113c, complete sequence) position: , mismatch: 7, identity: 0.767

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
aggaaggccgcgtcggcttcagcatcgaca	Protospacer
** *  . .**************.******

36. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP013493 (Rhizobium sp. N6212 plasmid pRspN6212c, complete sequence) position: , mismatch: 7, identity: 0.767

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
aggaaggccgcgtcggcttcagcatcgaca	Protospacer
** *  . .**************.******

37. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP013516 (Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence) position: , mismatch: 7, identity: 0.767

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
aggaaggccgcgtcggcttcagcatcgaca	Protospacer
** *  . .**************.******

38. spacer 3.58|979168|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

39. spacer 3.89|981352|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

40. spacer 3.90|981400|30|NZ_LS483523|CRT matches to NC_010553 (Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agttggcgaacgtcagcaagcaggtcagca	Protospacer
**.  . * ************* *******

41. spacer 3.92|981484|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

42. spacer 3.106|982216|30|NZ_LS483523|CRT matches to NC_010553 (Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agttggcgaacgtcagcaagcaggtcagca	Protospacer
**.  . * ************* *******

43. spacer 3.111|982420|30|NZ_LS483523|CRT matches to AP014939 (Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

44. spacer 3.111|982420|30|NZ_LS483523|CRT matches to NZ_LN681228 (Xenorhabdus nematophila AN6/1 plasmid II, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

45. spacer 3.111|982420|30|NZ_LS483523|CRT matches to NZ_AP018687 (Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

46. spacer 3.111|982420|30|NZ_LS483523|CRT matches to MT701594 (Streptomyces phage Spernnie, complete genome) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
cccgcaagcacgtccgcaacaacaagtacg	Protospacer
.* *****.********* *******..*.

47. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP027671 (Simplicispira suum strain SC1-8 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcaacaagcacctcgacaccgacg	Protospacer
***************.* ***** .*..*.

48. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP024314 (Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcaaaacgcgcgtcgacgccatgg	Protospacer
********** * ********** .**  .

49. spacer 3.116|982624|30|NZ_LS483523|CRT matches to NC_015065 (Granulicella tundricola MP5ACTX9 plasmid pACIX902, complete sequence) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
acaacaagtacatcggcatcaacgcggtag	Protospacer
 **.*******************. *   *

50. spacer 3.116|982624|30|NZ_LS483523|CRT matches to AP013475 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C83-MedDCM-OCT-S45-C54) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tactcaagttcatctgcatcaacaagcgat	Protospacer
*   ***** **** *************

51. spacer 3.116|982624|30|NZ_LS483523|CRT matches to NC_034248 (Rhizobium phage RHEph10, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcagccagtgcatcggcatcaacgtccgga	Protospacer
***** ***.*************.  ** .

52. spacer 3.116|982624|30|NZ_LS483523|CRT matches to MN096365 (Gordonia phage Samba, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
ccggcaactacatcggcatctacaagacca	Protospacer
.*.**** ************ *****  *.

53. spacer 3.116|982624|30|NZ_LS483523|CRT matches to MT639640 (Gordonia phage Paries, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
cgggcaactacatcggcatctacaagaccg	Protospacer
. .**** ************ *****  **

54. spacer 3.116|982624|30|NZ_LS483523|CRT matches to MK977702 (Gordonia terrae phage McKinley, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
cgggcaactacatcggcatctacaagaccg	Protospacer
. .**** ************ *****  **

55. spacer 3.258|985900|30|NZ_LS483523|CRT matches to JN106170 (Uncultured bacterium plasmid pAKD25, complete sequence) position: , mismatch: 7, identity: 0.767

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
gcaaagccagcaagtacagcagcaagcacg	Protospacer
.  * *.*******.*** ***********

56. spacer 3.258|985900|30|NZ_LS483523|CRT matches to JN106175 (Uncultured bacterium plasmid pAKD34, complete sequence) position: , mismatch: 7, identity: 0.767

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
gcaaagccagcaagtacagcagcaagcacg	Protospacer
.  * *.*******.*** ***********

57. spacer 3.258|985900|30|NZ_LS483523|CRT matches to JN106167 (Uncultured bacterium plasmid pAKD16, complete sequence) position: , mismatch: 7, identity: 0.767

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
gcaaagccagcaagtacagcagcaagcacg	Protospacer
.  * *.*******.*** ***********

58. spacer 3.264|986128|30|NZ_LS483523|CRT matches to MK759884 (Salmonella phage vB_SenM_SB18, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

59. spacer 3.264|986128|30|NZ_LS483523|CRT matches to NC_015292 (Erwinia phage phiEa104, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

60. spacer 3.264|986128|30|NZ_LS483523|CRT matches to MH426725 (Erwinia phage SunLIRen, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

61. spacer 3.264|986128|30|NZ_LS483523|CRT matches to FQ482083 (Erwinia amylovora phage phiEa104 complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

62. spacer 3.264|986128|30|NZ_LS483523|CRT matches to NC_011811 (Erwinia phage phiEa21-4, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

63. spacer 3.264|986128|30|NZ_LS483523|CRT matches to MG589384 (Enterobacter phage phi63_307, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

64. spacer 3.264|986128|30|NZ_LS483523|CRT matches to MK770412 (Salmonella phage SE5, complete genome) position: , mismatch: 7, identity: 0.767

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
acctcatcagcttcgactgttacaagtctg	Protospacer
* * **********.** ********* .

65. spacer 3.284|974722|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

66. spacer 3.290|975046|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

67. spacer 3.302|975514|30|NZ_LS483523|CRT matches to NC_010553 (Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agttggcgaacgtcagcaagcaggtcagca	Protospacer
**.  . * ************* *******

68. spacer 3.303|975562|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

69. spacer 3.305|975682|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

70. spacer 3.315|976270|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

71. spacer 3.317|976360|30|NZ_LS483523|CRT matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcgtcgacctcagcaagcacgtcagca--	CRISPR spacer
cccgcgtcgacctcagcatgcac--caactga	Protospacer
  **************** ****  **.*

72. spacer 3.331|976984|30|NZ_LS483523|CRT matches to NC_010553 (Burkholderia ambifaria MC40-6 plasmid pBMC401, complete sequence) position: , mismatch: 7, identity: 0.767

agcgcaagtacgtcagcaagcacgtcagca	CRISPR spacer
agttggcgaacgtcagcaagcaggtcagca	Protospacer
**.  . * ************* *******

73. spacer 3.336|977188|30|NZ_LS483523|CRT matches to AP014939 (Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

74. spacer 3.336|977188|30|NZ_LS483523|CRT matches to NZ_LN681228 (Xenorhabdus nematophila AN6/1 plasmid II, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

75. spacer 3.336|977188|30|NZ_LS483523|CRT matches to NZ_AP018687 (Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca-	CRISPR spacer
ggagcaagtacgtcctcatcaacaa-tgtac	Protospacer
  .************ ********* .*.*

76. spacer 3.336|977188|30|NZ_LS483523|CRT matches to MT701594 (Streptomyces phage Spernnie, complete genome) position: , mismatch: 7, identity: 0.767

tcggcaagtacgtccgcatcaacaagcgca	CRISPR spacer
cccgcaagcacgtccgcaacaacaagtacg	Protospacer
.* *****.********* *******..*.

77. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP027671 (Simplicispira suum strain SC1-8 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcaacaagcacctcgacaccgacg	Protospacer
***************.* ***** .*..*.

78. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP024314 (Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence) position: , mismatch: 7, identity: 0.767

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcaaaacgcgcgtcgacgccatgg	Protospacer
********** * ********** .**  .

79. spacer 3.341|977392|30|NZ_LS483523|CRT matches to NC_015065 (Granulicella tundricola MP5ACTX9 plasmid pACIX902, complete sequence) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
acaacaagtacatcggcatcaacgcggtag	Protospacer
 **.*******************. *   *

80. spacer 3.341|977392|30|NZ_LS483523|CRT matches to AP013475 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C83-MedDCM-OCT-S45-C54) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tactcaagttcatctgcatcaacaagcgat	Protospacer
*   ***** **** *************

81. spacer 3.341|977392|30|NZ_LS483523|CRT matches to NC_034248 (Rhizobium phage RHEph10, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcagccagtgcatcggcatcaacgtccgga	Protospacer
***** ***.*************.  ** .

82. spacer 3.341|977392|30|NZ_LS483523|CRT matches to MN096365 (Gordonia phage Samba, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
ccggcaactacatcggcatctacaagacca	Protospacer
.*.**** ************ *****  *.

83. spacer 3.341|977392|30|NZ_LS483523|CRT matches to MT639640 (Gordonia phage Paries, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
cgggcaactacatcggcatctacaagaccg	Protospacer
. .**** ************ *****  **

84. spacer 3.341|977392|30|NZ_LS483523|CRT matches to MK977702 (Gordonia terrae phage McKinley, complete genome) position: , mismatch: 7, identity: 0.767

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
cgggcaactacatcggcatctacaagaccg	Protospacer
. .**** ************ *****  **

85. spacer 3.381|983635|30|NZ_LS483523|CRT matches to AP014939 (Citrobacter freundii plasmid pKHM-1 DNA, complete sequence, strain: KHM 243) position: , mismatch: 7, identity: 0.767

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gcaagtacgtcctcatcaacaatgtaccgt	Protospacer
************ *********      **

86. spacer 3.381|983635|30|NZ_LS483523|CRT matches to NZ_LN681228 (Xenorhabdus nematophila AN6/1 plasmid II, complete sequence) position: , mismatch: 7, identity: 0.767

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gcaagtacgtcctcatcaacaatgtaccgt	Protospacer
************ *********      **

87. spacer 3.381|983635|30|NZ_LS483523|CRT matches to NZ_AP018687 (Vibrio rumoiensis strain FERM P-14531 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.767

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gcaagtacgtcctcatcaacaatgtaccgt	Protospacer
************ *********      **

88. spacer 3.381|983635|30|NZ_LS483523|CRT matches to MG592531 (Vibrio phage 1.164.O._10N.261.51.A7, partial genome) position: , mismatch: 7, identity: 0.767

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gctggtacgtctgcatcaccaagcgcagca	Protospacer
** .*******.****** ********.

89. spacer 3.381|983635|30|NZ_LS483523|CRT matches to MG592541 (Vibrio phage 1.174.O._10N.261.55.A8, partial genome) position: , mismatch: 7, identity: 0.767

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
gctggtacgtctgcatcatcaagcgcagca	Protospacer
** .*******.****** ********.

90. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP016722 (Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcaacaagcgcgtcgacctcagcaagc	CRISPR spacer
agtcaaacaagggcgtcgacctcagcaagt	Protospacer
.  . ****** *****************.

91. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NC_004444 (Pseudomonas resinovorans plasmid pCAR1, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcaa---caagcgcgtcgacctcagcaagc	CRISPR spacer
---tccagctcaagcgcgtcgacctcatcaact	Protospacer
   ** *   ***************** *** .

92. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NC_021506 (Pseudomonas resinovorans NBRC 106553 plasmid pCAR1.3, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcaa---caagcgcgtcgacctcagcaagc	CRISPR spacer
---tccagctcaagcgcgtcgacctcatcaact	Protospacer
   ** *   ***************** *** .

93. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NC_011838 (Pseudomonas putida plasmid pCAR1.2, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcaa---caagcgcgtcgacctcagcaagc	CRISPR spacer
---tccagctcaagcgcgtcgacctcatcaact	Protospacer
   ** *   ***************** *** .

94. spacer 3.390|983983|30|NZ_LS483523|CRT matches to MN224564 (Streptomyces phage Araceli, complete genome) position: , mismatch: 7, identity: 0.767

gcatcaacaagcgcaagtacgtcagcaagc	CRISPR spacer
acgccgacaagcgcgagtacgtccgcaagg	Protospacer
.*..*.********.******** *****

95. spacer 3.390|983983|30|NZ_LS483523|CRT matches to MH697589 (Microbacterium phage Neferthena, complete genome) position: , mismatch: 7, identity: 0.767

gcatcaacaagcgcaagtacgtcagcaagc---	CRISPR spacer
tcatcaacaagggcaaggacgt---cacgctca	Protospacer
 ********** ***** ****   ** **

96. spacer 3.390|983983|30|NZ_LS483523|CRT matches to MH229863 (Streptomyces phage JackieB, complete genome) position: , mismatch: 7, identity: 0.767

gcatcaacaagcgcaagtacgtcagcaagc	CRISPR spacer
acgccgacaagcgcgagtacgtccgcaagg	Protospacer
.*..*.********.******** *****

97. spacer 3.390|983983|30|NZ_LS483523|CRT matches to MH229862 (Streptomyces phage Henoccus, complete genome) position: , mismatch: 7, identity: 0.767

gcatcaacaagcgcaagtacgtcagcaagc	CRISPR spacer
acgccgacaagcgcgagtacgtccgcaagg	Protospacer
.*..*.********.******** *****

98. spacer 3.394|984139|30|NZ_LS483523|CRT matches to NZ_CP049158 (Caballeronia sp. SBC1 plasmid pSBC1_2, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcgacaagtgcaagcacatcggcgtca	CRISPR spacer
ccctcgacaagcgcaagcacaccggcaccg	Protospacer
 * ********.*********.****..*.

99. spacer 3.394|984139|30|NZ_LS483523|CRT matches to NZ_CP049318 (Caballeronia sp. SBC2 plasmid pSBC2-2, complete sequence) position: , mismatch: 7, identity: 0.767

gcatcgacaagtgcaagcacatcggcgtca	CRISPR spacer
ccctcgacaagcgcaagcacaccggcaccg	Protospacer
 * ********.*********.****..*.

100. spacer 3.395|984187|30|NZ_LS483523|CRT matches to MF580956 (Salinibacter virus M8CC-19, complete genome) position: , mismatch: 7, identity: 0.767

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
cgaagtacatcggcaagtccgaccgcaaac	Protospacer
  **************** ** *****

101. spacer 3.395|984187|30|NZ_LS483523|CRT matches to MF580959 (Salinibacter virus M8CRM-1, partial genome) position: , mismatch: 7, identity: 0.767

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
cgaagtacatcggcaagtccgaccgcaaac	Protospacer
  **************** ** *****

102. spacer 3.395|984187|30|NZ_LS483523|CRT matches to MF580960 (Salinibacter virus M31CC-1, partial genome) position: , mismatch: 7, identity: 0.767

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
cgaagtacatcggcaagtccgaccgcaaac	Protospacer
  **************** ** *****

103. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.767

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagtacatcggcaagaacttcaacaatg	Protospacer
***************** ** ** .** ..

104. spacer 3.395|984187|30|NZ_LS483523|CRT matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

gcaagtacatcggcaagtacgtccgcatca	CRISPR spacer
gcaagtacatcggcaagaacttcgacaatg	Protospacer
***************** ** ** .** ..

105. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP016722 (Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
gcaagtcaaacaagggcgtcgacctcagca	Protospacer
 *..  . ****** ***************

106. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP027023 (Streptomyces sp. WAC00288 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
cccacatcaagaagctcgtcgacctcaagg	Protospacer
.* .****** **** ***********. .

107. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aagacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

108. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP051294 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aggacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

109. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP033363 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aggacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

110. spacer 3.116|982624|30|NZ_LS483523|CRT matches to LR134127 (Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcaggaagtacatcggcaccaacatcattt	Protospacer
**** *************.*****    .

111. spacer 3.116|982624|30|NZ_LS483523|CRT matches to MN693854 (Marine virus AFVG_250M929, complete genome) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tctgcaagtacatctgcatcaactgcaacc	Protospacer
** *********** ******** .  .*

112. spacer 3.116|982624|30|NZ_LS483523|CRT matches to MN694256 (Marine virus AFVG_250M930, complete genome) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tctgcaagtacatctgcatcaactgcaacc	Protospacer
** *********** ******** .  .*

113. spacer 3.116|982624|30|NZ_LS483523|CRT matches to NZ_LR594668 (Variovorax sp. SRS16 plasmid 3) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
ccagcgagtacatcggcagcaacatcctga	Protospacer
.****.************ *****  *  .

114. spacer 3.116|982624|30|NZ_LS483523|CRT matches to NZ_CP016617 (Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcagcaagtacatcgggatcattccgttca	Protospacer
**************** **** .  *. *.

115. spacer 3.256|985816|30|NZ_LS483523|CRT matches to NZ_LN831184 (Vibrio cholerae isolate V. cholerae 116-14 plasmid pNDM-116-14, complete sequence) position: , mismatch: 8, identity: 0.733

tcgacctcagcaagcacgtcagcaagtaca	CRISPR spacer
ccaacctcagcaagcacctcaacaagctgg	Protospacer
.*.************** ***.****.  .

116. spacer 3.256|985816|30|NZ_LS483523|CRT matches to MN586060 (Mycobacterium phage PetterN, complete genome) position: , mismatch: 8, identity: 0.733

tcgacctcagcaagcacgtcagcaagtaca	CRISPR spacer
cacccgtcagccaccacgtcagcaagtacg	Protospacer
.   * ***** * ***************.

117. spacer 3.256|985816|30|NZ_LS483523|CRT matches to KT246486 (Mycobacterium phage Chadwick, complete genome) position: , mismatch: 8, identity: 0.733

tcgacctcagcaagcacgtcagcaagtaca	CRISPR spacer
cacccgtcagccaccacgtcagcaagtacg	Protospacer
.   * ***** * ***************.

118. spacer 3.258|985900|30|NZ_LS483523|CRT matches to MT227925 (Vibrio phage phiV141, complete genome) position: , mismatch: 8, identity: 0.733

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
gatgttaaagcaagcacatcagaaagcacg	Protospacer
..*..   ************** *******

119. spacer 3.258|985900|30|NZ_LS483523|CRT matches to MN582094 (Siphoviridae sp. ctjeG17, complete genome) position: , mismatch: 8, identity: 0.733

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
tttgcgacagcaagaacatcagcaagcgac	Protospacer
  *.** ******* ************.

120. spacer 3.258|985900|30|NZ_LS483523|CRT matches to HQ633071 (Synechococcus phage S-SKS1 genomic sequence) position: , mismatch: 8, identity: 0.733

agtacgtcagcaagcacatcagcaagcacg	CRISPR spacer
tgattatcagcaagcaaatcagaaagcact	Protospacer
 *  ..********** ***** ******

121. spacer 3.264|986128|30|NZ_LS483523|CRT matches to MH179480 (Pseudomonas phage 98PfluR60PP, complete genome) position: , mismatch: 8, identity: 0.733

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
agcacatcagcttcagcagctacgtcacca	Protospacer
***************.***.***.    *

122. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP016722 (Lactococcus lactis subsp. lactis strain UC11 plasmid pUC11C, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
gcaagtcaaacaagggcgtcgacctcagca	Protospacer
 *..  . ****** ***************

123. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP027023 (Streptomyces sp. WAC00288 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
cccacatcaagaagctcgtcgacctcaagg	Protospacer
.* .****** **** ***********. .

124. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aagacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

125. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP051294 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077A, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aggacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

126. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP033363 (Mesorhizobium sp. NZP2077 plasmid pMSNZP2077NSa, complete sequence) position: , mismatch: 8, identity: 0.733

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
aggacatcaacaagggcttcgacctcatgc	Protospacer
  *.********** ** *********

127. spacer 3.341|977392|30|NZ_LS483523|CRT matches to LR134127 (Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcaggaagtacatcggcaccaacatcattt	Protospacer
**** *************.*****    .

128. spacer 3.341|977392|30|NZ_LS483523|CRT matches to MN693854 (Marine virus AFVG_250M929, complete genome) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tctgcaagtacatctgcatcaactgcaacc	Protospacer
** *********** ******** .  .*

129. spacer 3.341|977392|30|NZ_LS483523|CRT matches to MN694256 (Marine virus AFVG_250M930, complete genome) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tctgcaagtacatctgcatcaactgcaacc	Protospacer
** *********** ******** .  .*

130. spacer 3.341|977392|30|NZ_LS483523|CRT matches to NZ_LR594668 (Variovorax sp. SRS16 plasmid 3) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
ccagcgagtacatcggcagcaacatcctga	Protospacer
.****.************ *****  *  .

131. spacer 3.341|977392|30|NZ_LS483523|CRT matches to NZ_CP016617 (Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

tcagcaagtacatcggcatcaacaagcgcg	CRISPR spacer
tcagcaagtacatcgggatcattccgttca	Protospacer
**************** **** .  *. *.

132. spacer 3.381|983635|30|NZ_LS483523|CRT matches to MH220877 (Oenococcus phage phiOE33PA, complete genome) position: , mismatch: 8, identity: 0.733

gcaagtacgtccgcatcaacaagcgcaagt	CRISPR spacer
atttttccgtccggaccaacaagcgcaagt	Protospacer
..   * ****** *.**************

133. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP027023 (Streptomyces sp. WAC00288 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.733

gcatcaacaagcgcgtcgacctcagcaagc	CRISPR spacer
acatcaagaagctcgtcgacctcaaggcac	Protospacer
.****** **** ***********. . .*

134. spacer 3.390|983983|30|NZ_LS483523|CRT matches to CP003186 (Thermoanaerobacterium phage THSA-485A, complete genome) position: , mismatch: 8, identity: 0.733

gcatcaacaagcgcaagtacgtcagcaagc	CRISPR spacer
atgccaacaagtgcaagtacgccagcagcc	Protospacer
....*******.*********.*****. *

135. spacer 3.55|979030|30|NZ_LS483523|CRT matches to NZ_CP015739 (Shinella sp. HZN7 plasmid pShin-03, complete sequence) position: , mismatch: 9, identity: 0.7

agtaccagtgcgtcggcttcagcgtcgaca	CRISPR spacer
ggggaagctgcgtcggcttcatcgtcgacc	Protospacer
.* .  . ************* *******

136. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP049701 (Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence) position: , mismatch: 9, identity: 0.7

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcagcaagcgcggcgacacttatt	Protospacer
*********.******** **** .. ..

137. spacer 3.112|982468|30|NZ_LS483523|CRT matches to NZ_CP049701 (Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence) position: , mismatch: 9, identity: 0.7

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcagcaagcgcggcgacacttatt	Protospacer
*********.******** **** .. ..

138. spacer 3.264|986128|30|NZ_LS483523|CRT matches to NC_049494 (Acinetobacter phage vB_AbaM_PhT2, complete genome) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
ccttttgcagcttcaacagttacaattgca	Protospacer
  . .  ****************** ***

139. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013499 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S39-C84) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

140. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013497 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S35-C79) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

141. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013498 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S38-C76) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

142. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013776 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C68A-MedDCM-OCT-S36-C73, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

143. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013496 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C68A-MedDCM-OCT-S28-C61) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

144. spacer 3.264|986128|30|NZ_LS483523|CRT matches to AP013775 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C68A-MedDCM-OCT-S26-C73, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.7

agcacatcagcttcaacagttacaagtgcc	CRISPR spacer
tcaacatcagcttctacagttacaccccac	Protospacer
   *********** *********  .  *

145. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP049701 (Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence) position: , mismatch: 9, identity: 0.7

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcagcaagcgcggcgacacttatt	Protospacer
*********.******** **** .. ..

146. spacer 3.337|977236|30|NZ_LS483523|CRT matches to NZ_CP049701 (Bradyrhizobium sp. 1S5 strain 323S2 plasmid pB323S2b, complete sequence) position: , mismatch: 9, identity: 0.7

tcggcatcaacaagcgcgtcgacctcagca	CRISPR spacer
tcggcatcagcaagcgcggcgacacttatt	Protospacer
*********.******** **** .. ..

147. spacer 3.383|983719|30|NZ_LS483523|CRT matches to NZ_CP028970 (Aminobacter sp. MSH1 plasmid pUSP2, complete sequence) position: , mismatch: 9, identity: 0.7

gcatcaacaagcgcgtcgacctcagcaagc	CRISPR spacer
caggcaacaagggcgtcgacctcatcatcg	Protospacer
  . ******* ************ **

148. spacer 3.90|981400|30|NZ_LS483523|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

149. spacer 3.90|981400|30|NZ_LS483523|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

150. spacer 3.90|981400|30|NZ_LS483523|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

151. spacer 3.106|982216|30|NZ_LS483523|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

152. spacer 3.106|982216|30|NZ_LS483523|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

153. spacer 3.106|982216|30|NZ_LS483523|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

154. spacer 3.302|975514|30|NZ_LS483523|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

155. spacer 3.302|975514|30|NZ_LS483523|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

156. spacer 3.302|975514|30|NZ_LS483523|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

157. spacer 3.331|976984|30|NZ_LS483523|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

158. spacer 3.331|976984|30|NZ_LS483523|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

159. spacer 3.331|976984|30|NZ_LS483523|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 13, identity: 0.567

agcgcaagtacgtcagcaagcacgtcagca------------	CRISPR spacer
------------tcggcaagcacgtcagcaagcacgcgacgc	Protospacer
            **.***************

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

79308 : 135709

Tupanvirus(16.67%)

transposase,tRNA,protease,holin

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000705428.1\|79308_79611_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC	NA	NA	NA	NA
WP_000143736.1\|79610_81077_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA	NA	NA	NA	NA
WP_023396168.1\|81076_82519_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB	NA	NA	NA	NA
WP_000224421.1\|82642_83686_+	2,3-butanediol dehydrogenase	A0A2K9L7I1	Tupanvirus	1.8e-10	24.4
WP_000568640.1\|84063_84624_+	elongation factor P	NA	NA	NA	NA
WP_000510591.1\|84645_85035_+	Asp23/Gls24 family envelope stress response protein	NA	NA	NA	NA
WP_000203654.1\|85027_85450_+	transcription antitermination factor NusB	NA	NA	NA	NA
WP_023396166.1\|85496_85874_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000148169.1\|86236_86422_-	biofilm-regulating peptide BriC	NA	NA	NA	NA
WP_053037948.1\|86564_87821_+\|transposase	ISL3 family transposase	A0A1S5SBP9	Streptococcus_phage	1.8e-222	91.6
WP_001017398.1\|88002_88770_-	acetyl-CoA carboxylase carboxyl transferase subunit alpha	NA	NA	NA	NA
WP_001173353.1\|88766_89633_-	acetyl-CoA carboxylase carboxyltransferase subunit beta	NA	NA	NA	NA
WP_000488675.1\|89669_91037_-	acetyl-CoA carboxylase biotin carboxylase subunit	NA	NA	NA	NA
WP_023396163.1\|91048_91471_-	3-hydroxyacyl-ACP dehydratase FabZ	NA	NA	NA	NA
WP_001052244.1\|91467_91953_-	acetyl-CoA carboxylase biotin carboxyl carrier protein	NA	NA	NA	NA
WP_000774063.1\|91955_93191_-	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_000763053.1\|93212_93944_-	3-oxoacyl-[acyl-carrier-protein] reductase	F2NZ40	Diadromus_pulchellus_ascovirus	2.2e-15	30.9
WP_000167622.1\|93977_94898_-	ACP S-malonyltransferase	NA	NA	NA	NA
WP_000857431.1\|94890_95865_-	enoyl-[acyl-carrier-protein] reductase FabK	NA	NA	NA	NA
WP_000257841.1\|95984_96209_-	acyl carrier protein	NA	NA	NA	NA
WP_000852956.1\|96268_97243_-	ketoacyl-ACP synthase III	NA	NA	NA	NA
WP_000386347.1\|97242_97677_-	MarR family transcriptional regulator	NA	NA	NA	NA
WP_000400073.1\|97770_98556_-	enoyl-CoA hydratase	NA	NA	NA	NA
WP_000869675.1\|98880_100245_+	aspartate kinase	NA	NA	NA	NA
WP_000079361.1\|100247_100619_+	DUF956 family protein	NA	NA	NA	NA
WP_000884262.1\|100832_102107_+\|tRNA	serine--tRNA ligase	A0A1B1IVT2	uncultured_Mediterranean_phage	3.3e-91	48.7
WP_000735959.1\|102131_103031_-	TDT family transporter	NA	NA	NA	NA
WP_000206761.1\|103140_103689_-	carboxymuconolactone decarboxylase family protein	NA	NA	NA	NA
WP_000891492.1\|103906_105229_-	sodium:alanine symporter family protein	NA	NA	NA	NA
WP_023396161.1\|105571_107908_-	endonuclease MutS2	Q94M10	Lactobacillus_phage	1.8e-21	50.0
WP_000622946.1\|108011_108560_-	CvpA family protein	NA	NA	NA	NA
WP_000002019.1\|108556_108859_-	cell division protein ZapA	NA	NA	NA	NA
WP_000146861.1\|108945_109818_+	ribonuclease HIII	NA	NA	NA	NA
WP_001048155.1\|109829_110444_+	signal peptidase I	NA	NA	NA	NA
WP_000454487.1\|110677_113044_+	ATP-dependent RecD-like DNA helicase	A0A0K2FLP8	Brevibacillus_phage	3.4e-57	27.1
WP_023396160.1\|113091_114375_-	trigger factor	NA	NA	NA	NA
WP_023396159.1\|115173_116310_-	mannitol-1-phosphate 5-dehydrogenase	NA	NA	NA	NA
WP_000764150.1\|116371_116809_-	PTS sugar transporter subunit IIA	NA	NA	NA	NA
WP_000927661.1\|116810_118766_-	transcription antiterminator	NA	NA	NA	NA
WP_054365916.1\|118789_120559_-	PTS mannitol transporter subunit IICBA	NA	NA	NA	NA
WP_023396156.1\|122041_123064_-\|holin	choline-binding protein CbpF	NA	NA	NA	NA
WP_001100138.1\|123082_123904_-\|protease	trypsin-like serine protease	NA	NA	NA	NA
WP_000754501.1\|123984_124224_-	hypothetical protein	NA	NA	NA	NA
WP_001823720.1\|124373_124646_-	DNA alkylation repair protein	NA	NA	NA	NA
WP_078102538.1\|124664_124979_-	DNA alkylation repair protein	NA	NA	NA	NA
WP_000698434.1\|125142_125775_-	response regulator transcription factor	NA	NA	NA	NA
WP_000743667.1\|125788_126784_-	sensor histidine kinase	NA	NA	NA	NA
WP_001224634.1\|126780_127479_-	cell wall-active antibiotics response protein	NA	NA	NA	NA
WP_000210629.1\|127556_128567_-	type 2 isopentenyl-diphosphate Delta-isomerase	NA	NA	NA	NA
WP_000562441.1\|128550_129558_-	phosphomevalonate kinase	NA	NA	NA	NA
WP_000373457.1\|129544_130498_-	diphosphomevalonate decarboxylase	NA	NA	NA	NA
WP_000163315.1\|130479_131358_-	mevalonate kinase	NA	NA	NA	NA
WP_000196978.1\|131479_131809_-\|transposase	transposase	NA	NA	NA	NA
WP_001835194.1\|132709_133297_+	lanthionine synthetase	NA	NA	NA	NA
WP_000765673.1\|133339_134572_+	MFS transporter	NA	NA	NA	NA
WP_023396153.1\|134689_135709_-\|holin	choline-binding protein CbpC	NA	NA	NA	NA

DBSCAN-SWA_2

144858 : 202864

Streptococcus_phage(40.0%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_053037948.1\|144858_146115_-\|transposase	ISL3 family transposase	A0A1S5SBP9	Streptococcus_phage	1.8e-222	91.6
WP_111683426.1\|146391_151695_-	YSIRK-type signal peptide-containing protein	NA	NA	NA	NA
WP_023396149.1\|151995_153978_-	peptide ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_001809483.1\|154176_154335_-\|transposase	transposase domain-containing protein	NA	NA	NA	NA
WP_000927991.1\|154927_155362_-\|transposase	transposase	A0A218MNE7	uncultured_virus	2.1e-05	24.6
WP_000600902.1\|155437_156289_-	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	1.5e-26	35.4
WP_000141502.1\|156354_157404_-	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	8.3e-72	44.5
WP_000131458.1\|157416_158010_-	dTDP-4-dehydrorhamnose 3,5-epimerase family protein	H9NC63	Sphingomonas_phage	3.9e-10	33.1
WP_023396148.1\|158010_158880_-	glucose-1-phosphate thymidylyltransferase RfbA	K7QKA7	Escherichia_phage	6.4e-102	64.2
WP_170835819.1\|159374_160793_-	hypothetical protein	NA	NA	NA	NA
WP_023396147.1\|160911_162255_-	oligosaccharide repeat unit polymerase	NA	NA	NA	NA
WP_023396577.1\|162254_163241_-	glycosyltransferase family 2 protein	NA	NA	NA	NA
WP_000029904.1\|163243_163963_-	CDP-alcohol phosphatidyltransferase family protein	NA	NA	NA	NA
WP_000701496.1\|164022_164199_-	LicD family protein	A0A1V0SD50	Indivirus	5.0e-06	55.1
WP_001028657.1\|164236_165181_-	glycosyltransferase family 8 protein	A0A2P0VP84	Tetraselmis_virus	4.2e-06	24.5
WP_001013464.1\|165276_166644_-	sugar transferase	NA	NA	NA	NA
WP_111683428.1\|166658_167348_-	tyrosine-protein kinase	A0A1X9I5D6	Streptococcus_phage	2.2e-73	62.8
WP_000664150.1\|167357_168050_-	capsular polysaccharide biosynthesis protein CpsC	A0A1X9I5E1	Streptococcus_phage	3.2e-64	58.5
WP_023396143.1\|168058_168790_-	capsular polysaccharide biosynthesis protein Cps4B	NA	NA	NA	NA
WP_000091054.1\|168791_170237_-	LCP family protein	A0A1X9I5X1	Streptococcus_phage	1.3e-131	60.1
WP_001808790.1\|170515_171862_-\|transposase	IS1380-like element ISSpn5 family transposase	A0A1X9I6F6	Streptococcus_phage	5.8e-78	40.0
WP_033604964.1\|172681_172849_-	S-ribosylhomocysteinase	NA	NA	NA	NA
WP_001156771.1\|173013_174621_-	alpha-glucosidase	NA	NA	NA	NA
WP_000743617.1\|174773_176258_+	DUF1846 domain-containing protein	NA	NA	NA	NA
WP_023396142.1\|176352_176835_+	S-ribosylhomocysteine lyase	NA	NA	NA	NA
WP_023396141.1\|177135_179241_-\|protease	ATP-dependent Clp protease ATP-binding subunit	H6X3M6	Enterobacteria_phage	2.2e-116	37.4
WP_000470835.1\|179804_180785_-	phospho-N-acetylmuramoyl-pentapeptide- transferase	NA	NA	NA	NA
WP_000872270.1\|180786_183039_-	penicillin-binding protein 2X	NA	NA	NA	NA
WP_000818547.1\|183042_183360_-	cell division protein FtsL	NA	NA	NA	NA
WP_000159408.1\|183371_184322_-	16S rRNA (cytosine(1402)-N(4))-methyltransferase RsmH	NA	NA	NA	NA
WP_001082472.1\|184487_184682_+	helix-turn-helix transcriptional regulator	I3VYZ1	Thermoanaerobacterium_phage	9.4e-06	42.6
WP_023396140.1\|184697_185240_+	DUF3278 domain-containing protein	NA	NA	NA	NA
WP_000711739.1\|185250_185493_+	hypothetical protein	NA	NA	NA	NA
WP_000838121.1\|185503_185839_+	hypothetical protein	NA	NA	NA	NA
WP_000412453.1\|185948_186950_-	LacI family DNA-binding transcriptional regulator	NA	NA	NA	NA
WP_001866206.1\|187009_188911_-	alginate lyase family protein	NA	NA	NA	NA
WP_000381738.1\|188932_189226_-	preprotein translocase subunit YajC	NA	NA	NA	NA
WP_000148019.1\|189225_190044_-	PTS mannose/fructose/sorbose transporter family subunit IID	NA	NA	NA	NA
WP_023396139.1\|190030_190810_-	PTS mannose/fructose/sorbose/N-acetylgalactosamine transporter subunit IIC	NA	NA	NA	NA
WP_001866207.1\|190824_191316_-	PTS system mannose/fructose/N-acetylgalactosamine-transporter subunit IIB	NA	NA	NA	NA
WP_000592946.1\|191326_192517_-	glycoside hydrolase family 88 protein	NA	NA	NA	NA
WP_023396138.1\|192528_192963_-	PTS sugar transporter subunit IIA	NA	NA	NA	NA
WP_000185877.1\|193233_194049_+	gluconate 5-dehydrogenase	NA	NA	NA	NA
WP_000684777.1\|194067_194709_+	RpiB/LacA/LacB family sugar-phosphate isomerase	NA	NA	NA	NA
WP_069286967.1\|194739_195741_+	sugar kinase	NA	NA	NA	NA
WP_023396137.1\|195750_196380_+	bifunctional 4-hydroxy-2-oxoglutarate aldolase/2-dehydro-3-deoxy-phosphogluconate aldolase	NA	NA	NA	NA
WP_023396136.1\|197522_200726_-	LPXTG-anchored hyaluronate lyase	NA	NA	NA	NA
WP_023396135.1\|200948_201425_+	glutathione peroxidase	NA	NA	NA	NA
WP_000436627.1\|201607_202864_+\|transposase	ISL3 family transposase	A0A1S5SBP9	Streptococcus_phage	9.5e-224	91.9

DBSCAN-SWA_3

310939 : 372699

Streptococcus_phage(35.29%)

tRNA,integrase,protease,bacteriocin

attL 309021:309037|attR 321706:321722

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
309021:309037	attL	NA	NA	NA	NA
WP_000811078.1\|310939_311449_-	hypothetical protein	A0A1X9I5V2	Streptococcus_phage	5.8e-47	53.9
WP_000173130.1\|311519_312050_-	hypothetical protein	A0A1X9I5U4	Streptococcus_phage	2.8e-36	48.7
WP_000865230.1\|312133_312301_-	hypothetical protein	NA	NA	NA	NA
WP_000434361.1\|312663_314133_-	DNA primase	Q9AZI5	Lactococcus_phage	8.1e-65	35.2
WP_000158192.1\|314185_315052_-	primase C-terminal domain-containing protein	A0A1X9I6L2	Streptococcus_phage	8.2e-126	75.0
WP_000492137.1\|315186_315468_-	hypothetical protein	A0A1X9I5U9	Streptococcus_phage	7.9e-30	67.8
WP_000058832.1\|315460_315802_-	hypothetical protein	NA	NA	NA	NA
WP_001003774.1\|315798_316014_-	hypothetical protein	NA	NA	NA	NA
WP_000174331.1\|316015_316216_-	hypothetical protein	NA	NA	NA	NA
WP_000141100.1\|316212_316665_-	hypothetical protein	NA	NA	NA	NA
WP_000424665.1\|317036_317663_-	Rha family transcriptional regulator	R9QNB1	Lactococcus_phage	2.1e-30	40.8
WP_001107589.1\|318060_318774_+	helix-turn-helix domain-containing protein	Q708R9	Streptococcus_phage	2.0e-16	51.9
WP_001233766.1\|318934_320449_+	putative DNA binding domain-containing protein	NA	NA	NA	NA
WP_000704664.1\|320533_321700_+\|integrase	site-specific integrase	A0A1X9I5Y5	Streptococcus_phage	3.7e-153	70.1
WP_000815629.1\|321860_322805_+	magnesium transporter CorA family protein	NA	NA	NA	NA
321706:321722	attR	NA	NA	NA	NA
WP_000078022.1\|322816_323500_+	DUF1129 domain-containing protein	NA	NA	NA	NA
WP_000255100.1\|323754_324786_+	LD-carboxypeptidase	NA	NA	NA	NA
WP_000987426.1\|324940_325618_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000166575.1\|325614_326178_-	DNA-3-methyladenine glycosylase I	NA	NA	NA	NA
WP_000271487.1\|326187_326781_-	Holliday junction branch migration protein RuvA	NA	NA	NA	NA
WP_001284096.1\|327185_328286_+	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A1V0SE20	Indivirus	3.8e-51	38.2
WP_000493838.1\|328270_328906_+	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	1.3e-43	46.9
WP_000456639.1\|328925_330131_+	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	3.5e-106	49.5
WP_001099505.1\|330131_330599_+	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	4.1e-39	52.0
WP_023396114.1\|330923_332873_-	DNA mismatch repair endonuclease MutL	A0A1B2LRQ5	Wolbachia_phage	3.8e-70	32.3
WP_000623387.1\|333155_333389_-	ROK family protein	NA	NA	NA	NA
WP_000792992.1\|333813_334992_-	MFS transporter	NA	NA	NA	NA
WP_000358548.1\|334988_336380_-	hypothetical protein	NA	NA	NA	NA
WP_000608717.1\|336355_337462_-	pyridoxal-dependent decarboxylase	NA	NA	NA	NA
WP_000358739.1\|337682_338240_-	phosphopantothenate--cysteine ligase family flavoprotein	A0A2H4X2C0	Flamingopox_virus	3.8e-15	34.0
WP_000537006.1\|338576_339443_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_000861967.1\|340026_340467_+	response regulator transcription factor	NA	NA	NA	NA
WP_000745055.1\|340463_340922_+	DUF3021 domain-containing protein	NA	NA	NA	NA
WP_000075789.1\|341231_342494_+	divalent metal cation transporter	NA	NA	NA	NA
WP_000849621.1\|342786_343257_-	class Ib ribonucleoside-diphosphate reductase assembly flavoprotein NrdI	NA	NA	NA	NA
WP_000729031.1\|343334_343868_-	hypothetical protein	NA	NA	NA	NA
WP_000278869.1\|343919_345206_-	response regulator transcription factor	NA	NA	NA	NA
WP_172448733.1\|345217_346864_-	sensor histidine kinase	NA	NA	NA	NA
WP_000532354.1\|346865_347480_-	YesL family protein	NA	NA	NA	NA
WP_000748394.1\|347614_348184_+	MptD family putative ECF transporter S component	NA	NA	NA	NA
WP_000444642.1\|348213_348906_-	ABC transporter permease	NA	NA	NA	NA
WP_000085677.1\|348907_349969_-	methionine ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	6.7e-29	35.7
WP_000231787.1\|349961_351335_-	M20/M25/M40 family metallo-hydrolase	NA	NA	NA	NA
WP_000694504.1\|351434_352289_-	MetQ/NlpA family ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_000724951.1\|352442_353273_-	amino acid ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_000253918.1\|353376_353700_-	AzlD domain-containing protein	NA	NA	NA	NA
WP_001141662.1\|353689_354346_-	AzlC family ABC transporter permease	NA	NA	NA	NA
WP_023396111.1\|354844_356071_-	MFS transporter	NA	NA	NA	NA
WP_000720788.1\|356142_356808_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000738307.1\|356819_357497_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000933479.1\|357518_357752_-	hypothetical protein	NA	NA	NA	NA
WP_023396110.1\|358037_358901_-	hypothetical protein	NA	NA	NA	NA
WP_023396559.1\|359295_360468_-	nucleotide sugar dehydrogenase	O41091	Paramecium_bursaria_Chlorella_virus	1.2e-79	43.8
WP_000069858.1\|360480_361230_-	PIG-L family deacetylase	NA	NA	NA	NA
WP_001813545.1\|361241_362741_-	asparagine synthase	NA	NA	NA	NA
WP_001835163.1\|362975_363653_-	hypothetical protein	NA	NA	NA	NA
WP_000288029.1\|363672_365289_-	ABC transporter ATP-binding protein	A0A1V0SE00	Indivirus	3.0e-28	36.0
WP_000375708.1\|365298_366252_-	glycosyltransferase family 2 protein	NA	NA	NA	NA
WP_000655041.1\|370064_371075_-\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD	NA	NA	NA	NA
WP_000569851.1\|371064_371502_-	ribosomal protein S18-alanine N-acetyltransferase	NA	NA	NA	NA
WP_000865691.1\|371498_372182_-\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex dimerization subunit type 1 TsaB	NA	NA	NA	NA
WP_000180803.1\|372359_372545_+\|bacteriocin	fratricide two-peptide bacteriocin subunit CibA	NA	NA	NA	NA
WP_000977347.1\|372546_372699_+\|bacteriocin	fratricide two-peptide bacteriocin subunit CibB	NA	NA	NA	NA

DBSCAN-SWA_4

449057 : 460513

Synechococcus_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000717506.1\|449057_449603_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	7.4e-24	35.0
WP_000182582.1\|449599_450622_-	phosphoribosylformylglycinamidine cyclo-ligase	A0A1D7SE90	Cyanophage	1.6e-64	43.9
WP_000220632.1\|450658_452101_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	5.7e-55	35.1
WP_023396094.1\|452193_455919_-	phosphoribosylformylglycinamidine synthase	A6N228	Microbacterium_phage	6.2e-37	26.2
WP_000043300.1\|456120_456828_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A1D8KNF0	Synechococcus_phage	1.8e-41	39.2
WP_023396757.1\|456997_458347_-	HlyD family secretion protein	NA	NA	NA	NA
WP_000668282.1\|458359_460513_-	peptide cleavage/export ABC transporter	W8CYL7	Bacillus_phage	3.6e-45	28.5

DBSCAN-SWA_5

488884 : 552878

Streptococcus_phage(38.89%)

transposase,tRNA,protease,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_001208988.1\|488884_490162_-\|tRNA	tRNA lysidine(34) synthetase TilS	A7K9Y8	Acanthocystis_turfacea_chlorella_virus	2.5e-06	24.1
WP_001224749.1\|490158_491427_-	serine hydrolase	NA	NA	NA	NA
WP_000041909.1\|491546_491915_-	septum formation initiator family protein	NA	NA	NA	NA
WP_001234978.1\|491907_492174_-	RNA-binding S4 domain-containing protein	NA	NA	NA	NA
WP_000258080.1\|492231_495741_-	transcription-repair coupling factor	NA	NA	NA	NA
WP_000163933.1\|495741_496311_-\|tRNA	aminoacyl-tRNA hydrolase	NA	NA	NA	NA
WP_001218707.1\|496381_497497_-	redox-regulated ATPase YchF	NA	NA	NA	NA
WP_000285194.1\|497580_497775_-	DUF951 family protein	NA	NA	NA	NA
WP_000581157.1\|497839_498976_-	DNA polymerase III subunit beta	A0A0A8IL17	Aurantimonas_phage	1.6e-23	24.4
WP_000660615.1\|499134_500496_-	chromosomal replication initiator protein DnaA	NA	NA	NA	NA
WP_000410383.1\|500708_501467_-	ParB/RepB/Spo0J family partition protein	S5VSZ7	Leptospira_phage	1.6e-16	36.1
WP_000681601.1\|501524_502706_-\|protease	serine protease	A0A1B1IT49	uncultured_Mediterranean_phage	1.5e-16	26.1
WP_000695929.1\|502888_503368_+	23S rRNA (pseudouridine(1915)-N(3))-methyltransferase RlmH	NA	NA	NA	NA
WP_000799689.1\|503649_503775_+	competence-stimulating peptide ComC	NA	NA	NA	NA
WP_000362880.1\|503795_505121_+	sensor histidine kinase	NA	NA	NA	NA
WP_000866065.1\|505117_505870_+	response regulator transcription factor	NA	NA	NA	NA
WP_001158266.1\|506112_506655_-	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_000834682.1\|507968_510521_-	YfhO family protein	NA	NA	NA	NA
WP_000958769.1\|510582_512205_-	ATP-binding cassette domain-containing protein	A0A2K9L3Z8	Tupanvirus	7.6e-48	26.0
WP_000165444.1\|512410_513436_+\|tRNA	tryptophan--tRNA ligase	NA	NA	NA	NA
WP_000073428.1\|513587_515066_+	IMP dehydrogenase	A0A1V0SHK8	Klosneuvirus	2.2e-94	40.5
WP_000266661.1\|515116_516214_-	DNA replication/repair protein RecF	NA	NA	NA	NA
WP_000455903.1\|516216_516585_-	S4 domain-containing protein YaaA	A0A1X9I5V8	Streptococcus_phage	7.0e-18	57.3
WP_023396063.1\|516743_517994_+	insulinase family protein	A0A1X9I714	Streptococcus_phage	5.4e-94	42.5
WP_023396062.1\|517990_519274_+	insulinase family protein	A0A1E1EST3	Acanthamoeba_castellanii_mimivirus	1.9e-17	29.5
WP_001227958.1\|519315_520137_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_023396061.1\|520147_520693_+	CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase	NA	NA	NA	NA
WP_023396060.1\|520689_521517_+	energy-coupling factor transporter ATPase	G9BWD6	Planktothrix_phage	2.8e-22	32.9
WP_000510412.1\|521501_522341_+	energy-coupling factor transporter ATPase	W8CYL7	Bacillus_phage	1.1e-15	32.6
WP_000377893.1\|522333_523128_+	energy-coupling factor transporter transmembrane protein EcfT	NA	NA	NA	NA
WP_001078983.1\|523186_524005_+	rod shape-determining protein MreC	NA	NA	NA	NA
WP_001249454.1\|524004_524499_+	rod shape-determining protein MreD	NA	NA	NA	NA
WP_000727012.1\|524592_525771_+	CHAP domain-containing protein	NA	NA	NA	NA
WP_000268466.1\|525994_526774_+	30S ribosomal protein S2	NA	NA	NA	NA
WP_000808063.1\|526852_527893_+	elongation factor Ts	NA	NA	NA	NA
WP_000973416.1\|528138_528462_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_000841819.1\|528901_529300_+\|transposase	transposase	NA	NA	NA	NA
WP_000029860.1\|529496_530417_-	cysteine synthase A	A0A1X9I5K7	Streptococcus_phage	1.3e-137	80.7
WP_000395739.1\|530701_531337_-	YigZ family protein	A0A1X9I5T8	Streptococcus_phage	4.4e-76	71.5
WP_000867616.1\|531392_532691_+	DEAD/DEAH box helicase	A0A1X9I5S6	Streptococcus_phage	1.2e-165	66.6
WP_000649971.1\|532687_533350_+	ComF family protein	NA	NA	NA	NA
WP_000599104.1\|533429_533978_+	ribosome-associated translation inhibitor RaiA	NA	NA	NA	NA
WP_000715115.1\|534113_536087_+	DHH family phosphoesterase	NA	NA	NA	NA
WP_000864220.1\|536083_536536_+	50S ribosomal protein L9	NA	NA	NA	NA
WP_000852486.1\|536579_537932_+	replicative DNA helicase	A0A1P8VVQ6	Streptococcus_phage	6.3e-149	61.3
WP_001278167.1\|537933_538200_+	hypothetical protein	NA	NA	NA	NA
WP_000698569.1\|538288_539635_+\|holin	choline binding-anchored murein hydrolase CbpD	NA	NA	NA	NA
WP_000647692.1\|539890_540181_+	thiamine-binding protein	NA	NA	NA	NA
WP_001813866.1\|540143_540902_+	ABC transporter permease	NA	NA	NA	NA
WP_000754546.1\|540940_541948_+	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_000136224.1\|541947_542676_+	ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	1.0e-28	36.2
WP_001211273.1\|542794_543253_+	CtsR family transcriptional regulator	NA	NA	NA	NA
WP_023396059.1\|543254_545687_+\|protease	ATP-dependent Clp protease ATP-binding subunit	A0A223W0B1	Agrobacterium_phage	5.0e-128	40.6
WP_001024077.1\|546316_546970_+	two-component system response regulator RR06	NA	NA	NA	NA
WP_000594659.1\|546966_548307_+	two-component system sensor histidine kinase HK06	NA	NA	NA	NA
WP_000241935.1\|548389_548917_+	isoprenylcysteine carboxyl methyltransferase family protein	NA	NA	NA	NA
WP_023396057.1\|549194_551411_+\|holin	pneumococcal surface protein PspC, choline-binding form	NA	NA	NA	NA
WP_111683441.1\|551612_552878_-\|transposase	ISL3 family transposase	A0A1S5SBP9	Streptococcus_phage	2.5e-224	92.6

DBSCAN-SWA_6

878137 : 885469

uncultured_Mediterranean_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000351907.1\|878137_878866_+	segregation/condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	5.3e-09	22.3
WP_000105310.1\|878884_879454_+	segregation/condensation protein B	A0A1B1IVT7	uncultured_Mediterranean_phage	5.0e-15	34.9
WP_001222228.1\|879440_880163_+	rRNA pseudouridine synthase	NA	NA	NA	NA
WP_000821640.1\|880162_880405_+	membrane protein insertion efficiency factor YidD	A0A2H4PQM5	Staphylococcus_phage	1.3e-17	59.4
WP_000858260.1\|880629_881595_-	siderophore ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_000764306.1\|881690_882443_-	ABC transporter ATP-binding protein	W6JKT0	Anomala_cuprea_entomopoxvirus	5.6e-14	27.9
WP_001193668.1\|882439_883396_-	iron chelate uptake ABC transporter family permease subunit	NA	NA	NA	NA
WP_000777246.1\|883385_884345_-	ABC transporter permease	A0A2H4IY97	uncultured_Caudovirales_phage	4.0e-57	40.8
WP_000167843.1\|884767_885469_-	UDP-glucose 4-epimerase	A0A2K9L1R4	Tupanvirus	1.7e-33	35.1

DBSCAN-SWA_7

1180377 : 1187128

Streptococcus_phage(50.0%)

protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_069286974.1\|1180377_1180884_+	dihydrofolate reductase	G3MBI7	Bacillus_virus	3.3e-26	41.9
WP_000442276.1\|1180883_1181054_+	hypothetical protein	NA	NA	NA	NA
WP_000106346.1\|1181085_1182318_+\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	4.2e-131	59.0
WP_000422599.1\|1182326_1182914_+	YihA family ribosome biogenesis GTP-binding protein	NA	NA	NA	NA
WP_001140413.1\|1182924_1183305_+	RidA family protein	NA	NA	NA	NA
WP_000163033.1\|1183356_1184247_+	RNase adapter RapZ	A0A0R8VB27	Thermobifida_phage	3.9e-06	29.8
WP_001231086.1\|1184243_1185221_+	YvcK family protein	A1IMD5	Streptococcus_phage	1.2e-184	100.0
WP_000011310.1\|1185217_1186129_+	DNA-binding protein WhiA	Q7AWZ3	Streptococcus_phage	9.8e-154	99.3
WP_000081011.1\|1186162_1187128_-	NAD(P)/FAD-dependent oxidoreductase	Q9JRK7	Streptococcus_phage	2.8e-66	100.0

DBSCAN-SWA_8

1234944 : 1285135

Streptococcus_phage(26.67%)

transposase,tRNA,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_023396358.1\|1234944_1235952_+\|transposase	IS30 family transposase	H7BVY4	unidentified_phage	1.9e-36	36.4
WP_001054562.1\|1236026_1236227_+	F0F1 ATP synthase subunit C	NA	NA	NA	NA
WP_000392851.1\|1236261_1236978_+	F0F1 ATP synthase subunit A	NA	NA	NA	NA
WP_000558554.1\|1236991_1237486_+	F0F1 ATP synthase subunit B	NA	NA	NA	NA
WP_000359036.1\|1237485_1238022_+	F0F1 ATP synthase subunit delta	NA	NA	NA	NA
WP_023396357.1\|1238036_1239542_+	F0F1 ATP synthase subunit alpha	NA	NA	NA	NA
WP_000301210.1\|1239557_1240436_+	F0F1 ATP synthase subunit gamma	NA	NA	NA	NA
WP_000094360.1\|1240521_1241928_+	F0F1 ATP synthase subunit beta	NA	NA	NA	NA
WP_000068048.1\|1241938_1242358_+	F0F1 ATP synthase subunit epsilon	NA	NA	NA	NA
WP_000665619.1\|1242402_1243416_-	lactonase family protein	NA	NA	NA	NA
WP_000435439.1\|1243559_1244726_+	AI-2E family transporter	NA	NA	NA	NA
WP_001065960.1\|1244715_1245945_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_000120830.1\|1246090_1246732_+	amino acid ABC transporter permease	NA	NA	NA	NA
WP_000891772.1\|1246741_1247371_+	amino acid ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	1.2e-28	37.3
WP_000759188.1\|1247383_1248220_+	amino acid ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_069287061.1\|1248497_1248845_-	thioredoxin	NA	NA	NA	NA
WP_023396354.1\|1248955_1250674_-	phospho-sugar mutase	A0A1X9I671	Streptococcus_phage	9.8e-272	82.8
WP_001811209.1\|1250907_1251051_+\|transposase	transposase	NA	NA	NA	NA
WP_001811210.1\|1251017_1251233_+\|transposase	transposase	NA	NA	NA	NA
WP_000200307.1\|1251219_1251753_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_001842111.1\|1252092_1252347_+	hypothetical protein	NA	NA	NA	NA
WP_023396353.1\|1252457_1253537_+	MucBP domain-containing protein	NA	NA	NA	NA
WP_023396352.1\|1253494_1254172_+	LPXTG cell wall anchor domain-containing protein	NA	NA	NA	NA
WP_000348122.1\|1254395_1255265_+	aquaporin family protein	NA	NA	NA	NA
WP_001040724.1\|1256175_1257372_+	elongation factor Tu	A0A076FFS6	Aureococcus_anophage	7.3e-32	29.6
WP_000850585.1\|1258860_1259943_-	DEAD/DEAH box helicase	Q5GF26	Diachasmimorpha_longicaudata_entomopoxvirus	1.8e-37	31.3
WP_023396348.1\|1259939_1260917_-	Gfo/Idh/MocA family oxidoreductase	NA	NA	NA	NA
WP_002206302.1\|1261149_1261527_+\|transposase	PD-(D/E)XK nuclease family transposase	NA	NA	NA	NA
WP_050150846.1\|1261761_1263153_+	polysaccharide deacetylase family protein	NA	NA	NA	NA
WP_023396346.1\|1263266_1264109_+	aldo/keto reductase	A0A2H4PQR8	Staphylococcus_phage	1.7e-51	40.2
WP_000038736.1\|1265334_1266252_+\|tRNA	glycine--tRNA ligase subunit alpha	NA	NA	NA	NA
WP_023396345.1\|1266463_1268500_+\|tRNA	glycine--tRNA ligase subunit beta	NA	NA	NA	NA
WP_000371285.1\|1268541_1268799_+	DUF896 family protein	NA	NA	NA	NA
WP_000673694.1\|1268915_1270160_-	NAD(P)H-dependent oxidoreductase	A0A2P0ZL82	Lactobacillus_phage	1.7e-55	52.7
WP_000915928.1\|1270178_1270784_-	NAD(P)H-dependent oxidoreductase	A0A2P0ZL77	Lactobacillus_phage	2.2e-53	53.7
WP_000175407.1\|1270843_1271767_-	FAD:protein FMN transferase	NA	NA	NA	NA
WP_000036789.1\|1272060_1273440_+	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_000138517.1\|1273591_1274467_+	pyridoxal 5'-phosphate synthase lyase subunit PdxS	NA	NA	NA	NA
WP_000689945.1\|1274467_1275049_+	pyridoxal 5'-phosphate synthase glutaminase subunit PdxT	NA	NA	NA	NA
WP_001097983.1\|1275069_1275717_-	hemolysin III family protein	NA	NA	NA	NA
WP_000858730.1\|1275713_1276160_-	DUF1836 domain-containing protein	NA	NA	NA	NA
WP_023396343.1\|1276294_1276789_+	GNAT family N-acetyltransferase	M1PSC3	Streptococcus_phage	1.4e-42	52.1
WP_001170347.1\|1276788_1277319_+	methylated-DNA--[protein]-cysteine S-methyltransferase	M1PFU9	Streptococcus_phage	1.4e-46	54.3
WP_000889093.1\|1277312_1277669_+	arsenate reductase family protein	M1PLC0	Streptococcus_phage	1.2e-33	57.3
WP_023396342.1\|1277826_1278627_+	amino acid ABC transporter permease	NA	NA	NA	NA
WP_000590986.1\|1278626_1279370_+	amino acid ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	1.6e-29	41.0
WP_000926599.1\|1279447_1279672_+	DUF4059 family protein	NA	NA	NA	NA
WP_023396341.1\|1279737_1280649_+	thioredoxin-disulfide reductase	G3MA85	Bacillus_virus	8.5e-89	51.5
WP_000855753.1\|1280687_1281416_-	23S rRNA (guanosine(2251)-2'-O)-methyltransferase RlmB	NA	NA	NA	NA
WP_001272941.1\|1281460_1282072_-	peptide deformylase	E3SLL2	Synechococcus_phage	4.9e-16	42.4
WP_000972917.1\|1283670_1284498_+	Cof-type HAD-IIB family hydrolase	NA	NA	NA	NA
WP_000290648.1\|1284499_1285135_+\|holin	1-alkyl-2-acetylglycerophosphocholine esterase	A0A2K9L661	Tupanvirus	4.3e-07	28.2

DBSCAN-SWA_9

1348962 : 1412646

Bacillus_phage(33.33%)

holin,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_001061973.1\|1348962_1349808_+\|holin	phosphorylcholine transferase LicD	NA	NA	NA	NA
WP_000225897.1\|1349797_1350901_+	glycosyltransferase	NA	NA	NA	NA
WP_000446980.1\|1350902_1351889_+	glycosyltransferase family 2 protein	NA	NA	NA	NA
WP_000565082.1\|1351904_1353338_+	O-antigen polysaccharide polymerase Wzy family protein	NA	NA	NA	NA
WP_000461498.1\|1353366_1354401_+	hypothetical protein	NA	NA	NA	NA
WP_000782676.1\|1354600_1355338_+	adaptor protein MecA	NA	NA	NA	NA
WP_000216375.1\|1355488_1356775_+	homoserine dehydrogenase	NA	NA	NA	NA
WP_000692438.1\|1356776_1357646_+	homoserine kinase	NA	NA	NA	NA
WP_000818203.1\|1357940_1358879_+	peptide-methionine (R)-S-oxide reductase MsrB	NA	NA	NA	NA
WP_023396329.1\|1358936_1360661_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	1.9e-44	28.3
WP_000828825.1\|1360662_1362411_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	2.1e-48	29.5
WP_001858999.1\|1362802_1364062_+	TRZ/ATZ family protein	NA	NA	NA	NA
WP_001287278.1\|1364311_1364812_+	50S ribosomal protein L10	NA	NA	NA	NA
WP_001196960.1\|1364887_1365256_+	50S ribosomal protein L7/L12	NA	NA	NA	NA
WP_001168348.1\|1365442_1365613_+	hypothetical protein	NA	NA	NA	NA
WP_000566537.1\|1366190_1366571_+	hypothetical protein	NA	NA	NA	NA
WP_000840778.1\|1366583_1366817_+	hypothetical protein	NA	NA	NA	NA
WP_111683457.1\|1366819_1367389_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000807141.1\|1367623_1367761_+	hypothetical protein	NA	NA	NA	NA
WP_172448732.1\|1367939_1370549_+	lanthionine synthetase	NA	NA	NA	NA
WP_001076602.1\|1370581_1372522_+	S9 family peptidase	NA	NA	NA	NA
WP_001108415.1\|1372518_1374126_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	6.0e-13	22.4
WP_000356590.1\|1374140_1374881_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	7.0e-09	30.8
WP_000945311.1\|1374883_1376203_+	FtsX-like permease family protein	NA	NA	NA	NA
WP_000718654.1\|1376335_1376473_+	hypothetical protein	NA	NA	NA	NA
WP_000711943.1\|1378943_1379114_+	hypothetical protein	NA	NA	NA	NA
WP_000199575.1\|1379609_1380956_-	NADP-specific glutamate dehydrogenase	NA	NA	NA	NA
WP_029645906.1\|1382658_1383177_+	hypothetical protein	NA	NA	NA	NA
WP_001808393.1\|1383233_1383518_-	type B 50S ribosomal protein L31	NA	NA	NA	NA
WP_000401775.1\|1383571_1384507_-	bifunctional oligoribonuclease/PAP phosphatase NrnA	NA	NA	NA	NA
WP_001162129.1\|1384610_1385054_+	flavodoxin	NA	NA	NA	NA
WP_000362435.1\|1385169_1385436_+	chorismate mutase	NA	NA	NA	NA
WP_000712098.1\|1385432_1385807_+	fluoride efflux transporter CrcB	NA	NA	NA	NA
WP_000237416.1\|1385800_1386130_+	fluoride efflux transporter CrcB	A0A2H4PQR0	Staphylococcus_phage	6.3e-10	37.8
WP_001068669.1\|1386248_1386596_+	50S ribosomal protein L19	NA	NA	NA	NA
WP_001009001.1\|1386875_1387874_-	SAP domain-containing protein	NA	NA	NA	NA
WP_000023518.1\|1387916_1388723_-	sugar-phosphatase	NA	NA	NA	NA
WP_001003501.1\|1388735_1390040_-	HD domain-containing protein	E3T4P8	Cafeteria_roenbergensis_virus	1.7e-26	30.2
WP_023396325.1\|1390111_1390489_+	DUF1934 domain-containing protein	NA	NA	NA	NA
WP_000402071.1\|1390579_1390912_+	putative DNA-binding protein	NA	NA	NA	NA
WP_000863628.1\|1390923_1392495_+	signal recognition particle protein	NA	NA	NA	NA
WP_000808288.1\|1392689_1393973_-	uracil transporter	Q9KX94	Enterobacteria_phage	4.0e-60	35.3
WP_000802934.1\|1394226_1394940_-	16S rRNA (guanine(527)-N(7))-methyltransferase RsmG	NA	NA	NA	NA
WP_000219847.1\|1395033_1395594_+	LemA family protein	NA	NA	NA	NA
WP_000895725.1\|1395595_1396495_+\|protease	zinc metalloprotease HtpX	NA	NA	NA	NA
WP_000558897.1\|1396538_1398098_-	ABC-F family ATP-binding cassette domain-containing protein	A0A1B0RXA0	Streptococcus_phage	9.3e-11	27.5
WP_000389597.1\|1398336_1398654_-	hypothetical protein	NA	NA	NA	NA
WP_023396323.1\|1398823_1399366_+	DUF177 domain-containing protein	NA	NA	NA	NA
WP_000244451.1\|1399365_1399995_+	endonuclease III	NA	NA	NA	NA
WP_000850024.1\|1400205_1400727_+	bifunctional pyr operon transcriptional regulator/uracil phosphoribosyltransferase PyrR	NA	NA	NA	NA
WP_001293845.1\|1400745_1401669_+	aspartate carbamoyltransferase catalytic subunit	M1HGA5	Paramecium_bursaria_Chlorella_virus	8.7e-25	31.7
WP_000166701.1\|1401718_1402798_+	glutamine-hydrolyzing carbamoyl-phosphate synthase small subunit	R4TGJ8	Halovirus	6.3e-59	35.9
WP_023396322.1\|1403110_1406287_+	carbamoyl-phosphate synthase large subunit	NA	NA	NA	NA
WP_001199657.1\|1406561_1407371_-\|holin	phosphorylcholine transferase LicD	A0A1V0SD50	Indivirus	2.6e-09	30.3
WP_000811992.1\|1407372_1408176_-\|holin	phosphorylcholine transferase LicD	A0A1V0SD50	Indivirus	5.3e-10	27.1
WP_000835918.1\|1408185_1409673_-	type IV teichoic acid flippase TacF	NA	NA	NA	NA
WP_000638482.1\|1410028_1410736_+	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase	NA	NA	NA	NA
WP_000609888.1\|1410740_1411763_+	alcohol dehydrogenase catalytic domain-containing protein	NA	NA	NA	NA
WP_023396321.1\|1411779_1412646_+\|holin	choline kinase LicA	NA	NA	NA	NA

DBSCAN-SWA_10

1452737 : 1460911

Bacillus_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000722076.1\|1452737_1453442_+	response regulator transcription factor	W8CYM9	Bacillus_phage	2.8e-39	39.8
WP_000886213.1\|1453434_1454784_+	cell wall metabolism sensor histidine kinase VicK	W8CYF6	Bacillus_phage	3.0e-34	34.0
WP_001289493.1\|1454785_1455595_+	MBL fold metallo-hydrolase	A0A0C5AFC1	Paenibacillus_phage	1.8e-34	39.0
WP_000208079.1\|1455685_1455928_+	hypothetical protein	NA	NA	NA	NA
WP_023396301.1\|1455929_1456184_+	type II toxin-antitoxin system RelE/ParE family toxin	A0A2P1N333	Gordonia_phage	1.1e-06	37.3
WP_023396300.1\|1456230_1457007_+	ion transporter	A0A1B0Y2S3	Lactobacillus_phage	6.0e-19	43.3
WP_000204727.1\|1457262_1458249_-	L-lactate dehydrogenase	NA	NA	NA	NA
WP_001152989.1\|1458442_1460911_+	DNA gyrase subunit A	G3M9Z5	Bacillus_virus	2.7e-105	35.5

DBSCAN-SWA_11

1516135 : 1522777

Streptococcus_phage(33.33%)

transposase,integrase

attL 1514116:1514129|attR 1525503:1525516

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
1514116:1514129	attL	NA	NA	NA	NA
WP_000201131.1\|1516135_1516915_-	ribonuclease HII	G4YAY0	Emiliania_huxleyi_virus	2.1e-24	37.1
WP_000201315.1\|1516901_1517753_-	ribosome biogenesis GTPase YlqF	NA	NA	NA	NA
WP_023396287.1\|1517834_1519343_-\|integrase	site-specific integrase	A0A1S5S9U4	Streptococcus_phage	8.4e-33	29.9
WP_000404196.1\|1519418_1519652_-	hypothetical protein	W6LM55	Streptococcus_phage	2.7e-15	53.3
WP_000286252.1\|1519953_1520175_-	helix-turn-helix transcriptional regulator	A0A1L2BY72	Clostridium_phage	3.9e-08	47.5
WP_001206385.1\|1520431_1520905_-\|transposase	IS200/IS605-like element ISSpn6 family transposase	A0A1P8BMC0	Lactococcus_phage	4.5e-17	32.9
WP_000642567.1\|1521062_1521863_-	ABC transporter permease	NA	NA	NA	NA
WP_000995575.1\|1521859_1522777_-	ABC transporter ATP-binding protein	W6JKT0	Anomala_cuprea_entomopoxvirus	6.9e-14	24.7
1525503:1525516	attR	NA	NA	NA	NA

DBSCAN-SWA_12

1732939 : 1742007

Streptococcus_phage(87.5%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_001166873.1\|1732939_1733818_-	16S rRNA (cytidine(1402)-2'-O)-methyltransferase	M1PLC5	Streptococcus_phage	3.9e-115	75.7
WP_000358228.1\|1733820_1734138_-	DNA replication initiation control protein YabA	M1PFV3	Streptococcus_phage	2.9e-28	60.0
WP_000806714.1\|1734177_1735068_-	DNA polymerase III subunit delta'	M1NSC1	Streptococcus_phage	4.9e-73	51.7
WP_000033396.1\|1735064_1735703_-	dTMP kinase	M1PSC7	Streptococcus_phage	1.1e-74	67.6
WP_000689693.1\|1735922_1736720_-	pyrroline-5-carboxylate reductase	A0A1X9I6T5	Streptococcus_phage	4.2e-60	50.6
WP_050295167.1\|1736723_1737986_-	glutamate-5-semialdehyde dehydrogenase	A0A1X9I5D4	Streptococcus_phage	1.9e-139	64.3
WP_073176995.1\|1737995_1739126_-	glutamate 5-kinase	A0A1X9I5D0	Streptococcus_phage	8.5e-115	58.7
WP_000403195.1\|1741119_1742007_-	RluA family pseudouridine synthase	A0A2H4UV25	Bodo_saltans_virus	1.3e-09	28.0

DBSCAN-SWA_13

2065550 : 2111591

Moumouvirus(20.0%)

transposase,tRNA,protease,bacteriocin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000591091.1\|2065550_2066894_-\|tRNA	cysteine--tRNA ligase	M1PG92	Moumouvirus	2.0e-46	35.5
WP_000613666.1\|2066975_2067860_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_000539998.1\|2067871_2068489_-	serine O-acetyltransferase	NA	NA	NA	NA
WP_001118973.1\|2068504_2070718_-	polyribonucleotide nucleotidyltransferase	NA	NA	NA	NA
WP_000089980.1\|2071402_2072269_-	methylenetetrahydrofolate reductase [NAD(P)H]	NA	NA	NA	NA
WP_000108186.1\|2072332_2074582_-	5-methyltetrahydropteroyltriglutamate-- homocysteine S-methyltransferase	NA	NA	NA	NA
WP_001819358.1\|2074842_2075109_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_000597993.1\|2075836_2076838_+	endonuclease/exonuclease/phosphatase family protein	NA	NA	NA	NA
WP_023396182.1\|2076905_2079311_-\|tRNA	phenylalanine--tRNA ligase subunit beta	NA	NA	NA	NA
WP_000619950.1\|2079387_2079897_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_001813261.1\|2079896_2080943_-\|tRNA	phenylalanine--tRNA ligase subunit alpha	A0A2I2L4E3	Orpheovirus	1.6e-27	32.8
WP_000151846.1\|2081424_2082840_-	glycoside hydrolase family 1 protein	A0A0B5JD41	Pandoravirus	3.3e-23	23.9
WP_000120586.1\|2082852_2084691_-	PTS glucose transporter subunit IIA	NA	NA	NA	NA
WP_000584538.1\|2084708_2085548_-	PRD domain-containing protein	NA	NA	NA	NA
WP_000842022.1\|2085847_2086030_-	hypothetical protein	NA	NA	NA	NA
WP_001192126.1\|2087476_2088280_-	Fic family protein	NA	NA	NA	NA
WP_001814829.1\|2088882_2090262_-	ATP-binding protein	NA	NA	NA	NA
WP_000516551.1\|2090312_2090477_-	DNA cytosine methyltransferase	NA	NA	NA	NA
WP_000032159.1\|2090557_2093209_-\|tRNA	valine--tRNA ligase	A0A1V0S951	Catovirus	1.2e-151	41.2
WP_000550023.1\|2093201_2093780_-	AAA family ATPase	NA	NA	NA	NA
WP_000124537.1\|2093779_2094340_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_075575731.1\|2094326_2094818_-	flavin reductase family protein	NA	NA	NA	NA
WP_000038625.1\|2095187_2095583_-	hypothetical protein	NA	NA	NA	NA
WP_000119708.1\|2095678_2095933_-	DUF1912 family protein	NA	NA	NA	NA
WP_000752892.1\|2095942_2097277_-	DUF438 domain-containing protein	NA	NA	NA	NA
WP_000368737.1\|2097276_2097510_-	DUF1858 domain-containing protein	NA	NA	NA	NA
WP_001068159.1\|2097969_2098152_-	hypothetical protein	NA	NA	NA	NA
WP_000840389.1\|2098153_2098933_-	hypothetical protein	NA	NA	NA	NA
WP_001273601.1\|2099211_2099562_-	30S ribosome-binding factor RbfA	NA	NA	NA	NA
WP_000039202.1\|2099812_2102605_-	translation initiation factor IF-2	A0A2H4UTS4	Bodo_saltans_virus	3.3e-19	22.9
WP_001041390.1\|2102621_2102921_-	YlxQ-related RNA-binding protein	NA	NA	NA	NA
WP_000857562.1\|2102913_2103207_-	YlxR family protein	NA	NA	NA	NA
WP_000032273.1\|2103228_2104365_-	transcription termination/antitermination protein NusA	NA	NA	NA	NA
WP_001810863.1\|2104408_2104888_-	ribosome maturation factor RimP	NA	NA	NA	NA
WP_001266083.1\|2105013_2105649_-\|tRNA	tRNA (guanosine(46)-N7)-methyltransferase TrmB	NA	NA	NA	NA
WP_000363002.1\|2105645_2106440_-	phosphotransferase family protein	NA	NA	NA	NA
WP_000394049.1\|2106600_2107212_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_001818347.1\|2107362_2107596_-	hypothetical protein	NA	NA	NA	NA
WP_000760510.1\|2107637_2108327_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_000877381.1\|2108378_2108762_-	hypothetical protein	NA	NA	NA	NA
WP_000346296.1\|2109547_2109667_-	hypothetical protein	NA	NA	NA	NA
WP_001820573.1\|2109770_2109920_-\|bacteriocin	bacteriocin-like peptide BlpO	NA	NA	NA	NA
WP_001099492.1\|2110163_2110367_-\|bacteriocin	two-peptide bacteriocin subunit BlpN	NA	NA	NA	NA
WP_000379877.1\|2110382_2110637_-\|bacteriocin	two-peptide bacteriocin subunit BlpM	NA	NA	NA	NA
WP_100214365.1\|2110786_2111591_-\|transposase	IS5 family transposase	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_LS483523

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection