CRISPRimmunity

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP040915	Georgenia sp. Z443 chromosome, complete genome	10 crisprs	WYL,cas3,csa3,DEDDh,DinG,cas4	3	13	3	0

1. NZ_CP040915

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP040915_1

• CRISPR_ID: NZ_CP040915_1
• CRISPR_location: 667151-667232
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_1

Consensus_repeat	Method
CCCGGAGCCGGCACCGCCACGCCCG	CRISPRCasFinder

spacers of NZ_CP040915_1

>1.1|667176|32|NZ_CP040915|CRISPRCasFinder
CCGGCACCGCCACGCCCGGAGCCGGCACCGCC

CRISPR arrays and Neighbor proteins around NZ_CP040915_1

CRISPR arrays

The CRISPR arrays of NZ_CP040915_1

>merge|NZ_CP040915|1|667151-667232|CRISPRCasFinder
CCCGCCGCCGCCACCGCCCCCGGAGCCGGCACCGCCACGCCCGGAGCCGGCACCGCCACGCCCGCCCGCGCCGCCACGCCCG

>NZ_CP040915|1|1|667151-667232|CRISPRCasFinder
CCCGCCGCCGCCACCGCCCCCGGAG	CCGGCACCGCCACGCCCGGAGCCGGCACCGCC
ACGCCCGCCCGCGCCGCCACGCCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927185.1|658876_659266_-|universal-stress-protein	unknown	unknown	gnl|CDD|366180
NZ_CP040915.1|WP_139931287.1|677195_678197_-|ornithine-carbamoyltransferase	unknown	unknown	gnl|CDD|179366
NZ_CP040915.1|WP_139927183.1|655622_656882_-|ornithine--oxo-acid-transaminase	unknown	unknown	gnl|CDD|179736
NZ_CP040915.1|WP_139927182.1|654409_655333_+|universal-stress-protein	unknown	unknown	gnl|CDD|366180
NZ_CP040915.1|WP_139927198.1|676209_677190_-|carbamate-kinase	unknown	unknown	gnl|CDD|183466
NZ_CP040915.1|WP_139927194.1|669709_670159_-|hypothetical-protein	unknown	unknown	gnl|CDD|376946
NZ_CP040915.1|WP_139927193.1|669107_669713_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225767
NZ_CP040915.1|WP_139927184.1|657339_658788_+|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl|CDD|224220
NZ_CP040915.1|WP_139927197.1|674895_676023_-|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|224747
NZ_CP040915.1|WP_139927187.1|660190_660661_-|DUF4383-domain-containing-protein	unknown	unknown	gnl|CDD|379556
NZ_CP040915.1|WP_139927196.1|672654_673428_-|creatininase	unknown	unknown	gnl|CDD|275241
NZ_CP040915.1|WP_168205554.1|673427_674564_-|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP040915.1|WP_139931283.1|671104_672640_-|cytosine-permease	unknown	unknown	gnl|CDD|271377
NZ_CP040915.1|WP_139931281.1|660806_662492_-|RecQ-family-ATP-dependent-DNA-helicase	unknown	unknown	gnl|CDD|223588
NZ_CP040915.1|WP_139927192.1|668369_668894_+|flavodoxin	unknown	unknown	gnl|CDD|365983
NZ_CP040915.1|WP_139927188.1|663802_664576_-|SARP-family-transcriptional-regulator	unknown	unknown	gnl|CDD|226156
NZ_CP040915.1|WP_139927186.1|659314_660184_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|235628
NZ_CP040915.1|WP_139927195.1|670155_671091_-|acetylglutamate-kinase	unknown	unknown	gnl|CDD|234869
NZ_CP040915.1|WP_139927189.1|664858_665053_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927190.1|665095_665302_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927185.1|658876_659266_-|universal-stress-protein	gnl|CDD|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	1.35137e-14
NZ_CP040915.1|WP_139931287.1|677195_678197_-|ornithine-carbamoyltransferase	gnl|CDD|179366	PRK02102, PRK02102, ornithine carbamoyltransferase; Validated.	0
NZ_CP040915.1|WP_139927183.1|655622_656882_-|ornithine--oxo-acid-transaminase	gnl|CDD|179736	PRK04073, rocD, ornithine--oxo-acid transaminase; Provisional.	4.97827e-160
NZ_CP040915.1|WP_139927182.1|654409_655333_+|universal-stress-protein	gnl|CDD|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	3.40715e-21
NZ_CP040915.1|WP_139927198.1|676209_677190_-|carbamate-kinase	gnl|CDD|183466	PRK12354, PRK12354, carbamate kinase; Reviewed.	0
NZ_CP040915.1|WP_139927194.1|669709_670159_-|hypothetical-protein	gnl|CDD|376946	pfam02863, Arg_repressor_C, Arginine repressor, C-terminal domain.	3.4498e-17
NZ_CP040915.1|WP_139927193.1|669107_669713_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|225767	COG3226, COG3226, Uncharacterized protein conserved in bacteria [Function unknown].	6.17927e-08
NZ_CP040915.1|WP_139927184.1|657339_658788_+|cation:dicarboxylase-symporter-family-transporter	gnl|CDD|224220	COG1301, GltP, Na+/H+-dicarboxylate symporters [Energy production and conversion].	9.44297e-111
NZ_CP040915.1|WP_139927197.1|674895_676023_-|serine/threonine-protein-kinase	gnl|CDD|224747	COG1834, COG1834, N-Dimethylarginine dimethylaminohydrolase [Amino acid transport and metabolism].	6.52443e-14
NZ_CP040915.1|WP_139927187.1|660190_660661_-|DUF4383-domain-containing-protein	gnl|CDD|379556	pfam14325, DUF4383, Domain of unknown function (DUF4383). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 137 and 164 amino acids in length.	5.04364e-31
NZ_CP040915.1|WP_168205554.1|673427_674564_-|DMT-family-transporter	gnl|CDD|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	8.13842e-14
NZ_CP040915.1|WP_139931283.1|671104_672640_-|cytosine-permease	gnl|CDD|271377	cd11484, SLC-NCS1sbd_CobB-like, nucleobase-cation-symport-1 (NCS1) transporter CobB-like; solute-binding domain. This NCS1 subfamily includes Escherichia coli CodB (cytosine permease), and the Saccharomyces cerevisiae transporters: Fcy21p (Purine-cytosine permease), and vitamin B6 transporter Tpn1. NCS1s are essential components of salvage pathways for nucleobases and related metabolites; their known substrates include allantoin, uracil, thiamine, and nicotinamide riboside. NCS1s belong to a superfamily which also contains the solute carrier 5 family sodium/glucose transporters (SLC5s), and solute carrier 6 family neurotransmitter transporters (SLC6s).	9.80259e-69
NZ_CP040915.1|WP_139931281.1|660806_662492_-|RecQ-family-ATP-dependent-DNA-helicase	gnl|CDD|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	9.52188e-132
NZ_CP040915.1|WP_139927192.1|668369_668894_+|flavodoxin	gnl|CDD|365983	pfam00258, Flavodoxin_1, Flavodoxin.	2.35483e-06
NZ_CP040915.1|WP_139927188.1|663802_664576_-|SARP-family-transcriptional-regulator	gnl|CDD|226156	COG3629, DnrI, DNA-binding transcriptional activator of the SARP family [Signal transduction mechanisms].	3.07485e-22
NZ_CP040915.1|WP_139927186.1|659314_660184_-|alpha/beta-fold-hydrolase	gnl|CDD|235628	PRK05855, PRK05855, SDR family oxidoreductase.	1.51021e-37
NZ_CP040915.1|WP_139927195.1|670155_671091_-|acetylglutamate-kinase	gnl|CDD|234869	PRK00942, PRK00942, acetylglutamate kinase; Provisional.	5.93729e-142
NZ_CP040915.1|WP_139927196.1|672654_673428_-|creatininase	gnl|CDD|275241	TIGR04448, creatininase, creatininase. Members of this family are creatininase (EC 3.5.2.10), an amidohydrolase that interconverts creatinine + H(2)O with creatine. It should not be confused with creatinase (EC 3.5.3.3), which hydrolyzes creatine to sarcosine plus urea. [Central intermediary metabolism, Nitrogen metabolism].	1.46294e-125

Protein sequences

>NZ_CP040915.1|WP_139927190.1|665095_665302_+|hypothetical-protein
MADHRTLMESELDAQALEVLPPRETLWLNLNINIAPVIAINNAVAIQMFTIDSVNIANAQQWVSVAQG
>NZ_CP040915.1|WP_139927189.1|664858_665053_+|hypothetical-protein
MRDLSFSEIDGQATELLPTKETLFFFKVNYADVYATNSATALQAYTWGSLNVANAEQYVQVNQY
>NZ_CP040915.1|WP_139927188.1|663802_664576_-|SARP-family-transcriptional-regulator
MDSEAIAISGHGPRWSLRLFDGWQLRCDDAAVVVAYRERRLISLLALQGERPRSHLAGLLWPESDESRAHGNLRAAVWRIQHLLVGVLQESPGMMTLASDVQVDVHELRTLAHRLTADEEPPDTAHALQVLRRGTLLPGWYDDWALEEREQLHQLRLRALENLADRLLERDQLDGALQAAMGAVSLEPLRESAHRALIRVHLRDGNHVEAVRVYRTFRERLNDELGISVSPLIVDLVRPLQTATERHNGPQQLRRRH
>NZ_CP040915.1|WP_139931281.1|660806_662492_-|RecQ-family-ATP-dependent-DNA-helicase
MAAAVAGRDVLAVMPTGYGKSAIYQVSAVLLDGPTIVVSPLISLQQDQVAGLEEAGSGVEAVAVNSAQDRRENAESWRTVGSGGAEFLFLSPEQLAKEDVTDRIRVLRPSLFVVDEAHCVSSWGHDFRPDYLALGAVVERVGRPVVIALTATASTPVQSEIVDRLGLRDPLVVSRGFDRPNLTLEVLRHPDDATKRRAVVDGVTNLAGPGLVYVATRKDTERYASALAERGLRAAVYHAGRSADDREQVHRAFLDDEVDVVVATSAFGMGIDKPNVRFVVHADAPDSLDSYYQEIGRAGRDGEAARAVLHYRPEDLGLRQYFATTSVDEPALRALLTAVRRAGGPAALTHLRERTGLSARKVAGLVNLLQEVGAVRRERRGVAAVGDEAPGRVVARAEDLTDSRERVNRSRVEMVRGYAETLECRRRFLLGYFGEPHPGGCGSCDVCRRDEPDMDDDGGPGVVEDVIAGTDVLEGTDRRPAPTPAMSSETTSTTREMSSSPPDVTAPDDQFPLQASVEHREWGPGVVMRHDGDRITVFFEREGYRTLDRELIAREDLLRRG
>NZ_CP040915.1|WP_139927187.1|660190_660661_-|DUF4383-domain-containing-protein
MARAENPTVRRPRGVHQWLALLVGAVFLAVGLWGFARTGLDGLTDPEVLTAHDGPTLLWFTVNPLHNIVHVVVGVLGVLLWAASATARIYGWLLFLGYGAVFVYGLFAVGNPDIDLLHLNQADNWLHLGTALVGLLIAVLPRPGPPVARDTPGVRP
>NZ_CP040915.1|WP_139927186.1|659314_660184_-|alpha/beta-fold-hydrolase
MDRLTTLRRGRLVFDVRDDGPDDGEPVVLLHGFPQDSSCWGKVAPLLHQVGLRTLALDQRGYSPGARPPGRGAYRLSWVAADVVALLDAAGLARAHLVGHDWGGAVTWAVAADAPERVASATVLSTPHPRAFARALPRSDQPLRSWYILFEQLPALPELLLRAGLQRGLRDRGLPAADAARYARRMREPGALTGALNWYRAIPFYATALPGRVRVPVTYVFGEHDFALSRSAAEGSAALVDGDYRFVALDAGHWLPETRPDEVARAVVDRVRSARGDLHHGHPDGLWDN
>NZ_CP040915.1|WP_139927185.1|658876_659266_-|universal-stress-protein
MTIVVGYTTRPEGRAALERAIVEAKAHEEDLVVLNVSEGDGVRDPLLASETDLDEVRGLLSHAGVEGKVRQLVRGKDAAEEIDSIATEVDASLVIIGLRKRTPVGKLVLGSNSQRILLTVDAPVLAVKA
>NZ_CP040915.1|WP_139927184.1|657339_658788_+|cation:dicarboxylase-symporter-family-transporter
MATTTTPGTAAPRRRLRLPSFSMQILIGLALGVLLGWLALSLGKTPEGEENWLTVTLSTIGSSFVNLLKAVVAPLVFTAIVASIANLRGVANGARLAGQTLLWFAITALVAVAIGIGLGLVMQPGVNSGVDAAEAGAPGRTGSWLDFLQGLIPLNFLGLGASSQLQTGDDGVISAVTTGVSFNVLQIIVIALAVGIAALKVGQKSEPFLTFNRSLLAVIQKVLWWIIRLAPLGTLGLVGRAIATYGWSSLTSLGTFAIAIYVGLALVVFVVYPILLKTHGLSVLSYFKGAWPAIELAFVSRSSIGTMPVTERVTHRNLGVPRGYASFAVPLGATTKMDGCAAIYPAIAAIFVAQFFGVSLSITDYLLIAFVSVVGSAATAGLTGATVMLTLTLSTLGLPLEGVGLLLAIDPILDMGRTAVNVAGQVLVPVIVAKREGILDVEQYRSANAEDLFTEDEDAELAQETADAAPAGQEPELAAARR
>NZ_CP040915.1|WP_139927183.1|655622_656882_-|ornithine--oxo-acid-transaminase
MLGHPDAPHAPAPRGAAVTPSALAPNYHPLPVVLATGEGSWVTDVHGRRYLDCLAGYSALNFGHRHPALVAAAKAQLDKITLTSRAFEHELLEPFARAVTELTGSEMLLPMNTGAEAVETAVKAARKWGYDVKGVPDEAATIVVTEGAFHGRTTTVVSMSEDPQMRDGFGPYTPGFRIVPYGDADAVAAAIDETTVAVLVEPVQGESGVIVPPADYLPRLRELCSATDVLLVLDEVQSGLGRTGTTLAQDLAGVRADLTTLGKALGGGILPVSAVVGRRDVLEVFSAGTHGSTFGGNSLACAVGLAVVDLLAPGDLQARAGALGVVLHERVEVLVARGLLAGARTVGLWAGLDVEPALGLSGYQTCQRLAARGILVKETHGTTIRLSPPLNIAEDDLHLALDTLTDVLHEEAVEAGRTP
>NZ_CP040915.1|WP_139927182.1|654409_655333_+|universal-stress-protein
MAHEKVVVVGVDGSEASLAAVDWAVAEAKRTGWRLHIVCAYALPSFTAASLDGGYAAMDDTAIQQGAQAVIDEALARTASSGVVVTSALEAGDPAGVLVDLSREASLVVVGTRGGGGFTDRLLGTVSSALPAHAHCPAVIVPVREGRSYTPVRRIVVGVDGSDSAKIALRRAVDEAALWDAELSAVAAVPIATGAGAMAWLPATVDRDEVLADVREGLGVAVTAAVGDRQVRVRQHALDGNAAALMAEFSTAVELVVVGTRGRGGFAGLLLGSTSQAVLHHAASPVMVVPARIKDEGLSPTDVPWNA
>NZ_CP040915.1|WP_139927192.1|668369_668894_+|flavodoxin
MDALVVYESMFGNTKAVAEAVAEGLTAGATRAQVCEVGEAPALEDLHVDLLVVGAPTQAFGLSRPQTRADAAARGGGSVISAGKGVREWLGAADHAPGGLRVAAFDTHVKTPMIPGWASHSEEKRLRRLGAKVVGKSRSFYVQGYTGPLLDGELDRARRWGEELAATVGGALVG
>NZ_CP040915.1|WP_139927193.1|669107_669713_-|TetR/AcrR-family-transcriptional-regulator
MSTAGRTATVTGRTAPEARRATDRGGRRRTEIAEVAAAILREEGPAGVSHRTVARRVGCSLSLTTYYFESLDELLAEAGRINIGLWASRAEAVAEAAETEPAPTERDAITALVLRACLPEGSELLGHYLQLIAAGGAAPVSTSYRTGRDRLNGAVARVLRRVECTRPPELVIAVVDGAAVSALSEGRDVREDAARLLDHIL
>NZ_CP040915.1|WP_139927194.1|669709_670159_-|hypothetical-protein
MSSPAPQQRPASRLGPVSRLGTAPRLSSVRAGAPPAEQQDETPEPLVGALQELVFTVREAENLVVLKTLRGAAPMVAAVIDDAMIAPIVATVAGNDTVLAITRSEVAGGIIARYFRSLAGVGPRRARPVTSSRAGTAALPGAAHDEESG
>NZ_CP040915.1|WP_139927195.1|670155_671091_-|acetylglutamate-kinase
MSTISLERPAAAFSTERDLLPHQKAEVLIQALPWLERFAGGRVVIKYGGHAMVDPALQRAFAQDVLFLHRVGLHPVVVHGGGPQISRMLDRLGIATEFRGGLRVTTPEVMDVVRMVLTGQVQRDLVGQLNTQVAHAVGISGEDGGLFRARRRRAVVDGEEVDVGMVGDVVTVNPQAVEDLLAADRIPVISTVAPDVADPGRVLNVNADTAAAALAVALHARKLVVLTDVEGLYPRWPHRHPLVRRMSASELAELLPRLESGMVPKMEACLRAVRGGVPQAHVIDGRREHSMLLEIFTDGDTGTMILPDGAM
>NZ_CP040915.1|WP_139931283.1|671104_672640_-|cytosine-permease
MNFTGARTPVTGTSLSGRDPASAGPAHTEPPDVRRDVEETLQPIPEDQRTTKVAGQFWIWAGANIAPINWVLGALGISMGLGLWDTFGVLVAGNVLGMVVFGLFVLLGQRSGVTGMLLGRGVFGRRGNYLPAVIQATVVIGWCAVNTWIVLDLVMALFGKIGLVDPTLTNYGWKFAVAAAVMAVQVTIALFGYRAISAFERWTVPPTIAILVAMSVAAWVFMDIDWSYAGPPTGALTGWERIVAMSSVMTAIGVGWGLTWLTYASDYSRFVSKTVPRKKLYLASAGGQILPVLWLGLLGATLATTNGSVDPGKLIVDNFGALAIPVLLLVLHGPIATNILNIYTFTVTIQSLDVRIGRRALNIGMGVATMGAVTVFVFSTDIASSLDAWLSACVGWTSTWGAIVGVRYYLLDRHSTDFGHHFDPVGTHRLRDVDWRALVAFGTGLLCAWLFMHGMVPALQGPVSTALHGLDLSWLAAAISSGGVYYLLVRKDPTLRGSRTRTGVASGTPTN
>NZ_CP040915.1|WP_139927196.1|672654_673428_-|creatininase
MARSVFMEDLDAFTYRERVADGAPVLIPVGSIEQHGPHMPLSVDVLLSKAMAGAVAERTGSLVAAPIVYGYKSQQRSGGGNHLTGSTSLDAATVIATAKSLVLELARHGVRKIAFVNGHYENYQFLYEGVDLALGELRLAGTEDVRVMLMSYWDFVDDAAIAELYPDGFPGWDLEHGGVLETSLMLLLHPHLVDMDRVADIPPAVLPTYDLLPARPEITPPSGCLSSGAAATAGKGRVLLDRASAGMVTAIRSEFGM
>NZ_CP040915.1|WP_168205554.1|673427_674564_-|DMT-family-transporter
MNPTKALKLKGFGIMFLSSSLMGGIGAFARYIDAPGDFIAFNRSLAGLIGMTAIFLATKGFLKVRATKFTPSLLLSGVFLGLLSSLYVISTQMTTLANASFLIYTGPIYSTVLSAIFLKEPLKKSMIASLGAVLVGTLLIIGIINYTAGDGFTVGLDLDPQYMTGNLVALVSGVAYGLYLFFSRYRTDCDSNVRAGFNFLFAVVTIGVILMFRTPDLSGMDSRSWIVLAIAAVVTGFGAFYFLTVATRILLAGELAVISYQETIMATVLGLVLFAEPLTGMQALGGVLIVGGGLSQILASTKARPKRADGPDAVGAAPDREPTTPVQSAPEPAPVIASTLTADPAEPTAAPAMASAATAAAPAVAAPTAGTRSSRRTN
>NZ_CP040915.1|WP_139927197.1|674895_676023_-|serine/threonine-protein-kinase
MTKIVNSWNDFDPLKHVIVGRADNSVIPPEEPATSEKVPVDSEMRGMWGPRPTETVEKANAQLDNYAKVLEGLGVKVDRPTPLQWNQEIKTPDFRTESGMTQMPPRDILLTIGNEIMASANSFRCRYFEYLAYWPLMNEYFEADPEFKWTQAPRPRLTDKSYKHNYYDEKITLEERLVRTANKDFVTTEAEPMWDAADVMRMGKDLFIQHGLTTNLKAMEWFKRYYPDLRVHSLNFPGDPYPIHIDATFVPLRPGLIINNPHRPLPEDQRKIFEANDWEIVSAATPAHDEPPALCYSSVWLSMNCLVVDHKTVIVEESEVYQAEQMDKLGMNVIPVPLRDAYAFGGGLHCATADVYREGGCEDYFPNQAGDTTLV
>NZ_CP040915.1|WP_139927198.1|676209_677190_-|carbamate-kinase
MRIVVALGGNALLQRGDKPDADIQIANVETAVKALAPLAEEHEVVITHGNGPQVGVLALQSANDANLTTPYPFDTLGAQTQGMIGYWLLQALQNNLPGRHVAALVNQTLVLAGDPAFKNPTKFVGEVYNEEQAEKLAAERGWVMKADGPYFRRVVGSPKPQRVIETRLIRTMLAAGAVVVCAGGGGVPVIRNEFGKLQGVEAVIDKDLTAAVLAEALEADVLMILTDVPAVMADYGTPQQREITRSTPGALRDLGLPAGSMGPKVEAACRFVELTGDMAAIGRLQDARDIIAGKAGTIVTPGGNYGGPDDIRPPVPQVPETRVRRA
>NZ_CP040915.1|WP_139931287.1|677195_678197_-|ornithine-carbamoyltransferase
MPHALHGRNFLKELDFTPDEWRSLLDLSAALKAEKKSGTELPRLAGKNIALIFEKTSTRTRCSFEVAAFDQGAHVTYLDPSGSQMGHKESVADTARVLGRFYDGIEFRGASQEAVEVLGAQSGVPVWNGLTDDWHPTQMLADQLTMREHSDKADGEIAFAYLGDARNNVGNSLLISGAMLGMDVRMVAPKELQNAPEIVAKAREIAAETGARITITDDVAVGVKGVDFLYTDVWVSMGEPKEVWDERITLLKDYQINAALVAATGNPDVKFLHCLPAFHDRGTKVGEDIYQKTGMDALEVTDEVFESPASIVFDQAENRMHTIKAVMVATLGS

Crispr_ID: NZ_CP040915_2

• CRISPR_ID: NZ_CP040915_2
• CRISPR_location: 1028901-1028979
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_2

Consensus_repeat	Method
CCGCGGTCGATGAAGCGTCAGGCGACGA	CRISPRCasFinder

spacers of NZ_CP040915_2

>2.1|1028929|23|NZ_CP040915|CRISPRCasFinder
AGCGTCAGCCGACGACGCGGCGC

CRISPR arrays and Neighbor proteins around NZ_CP040915_2

CRISPR arrays

The CRISPR arrays of NZ_CP040915_2

>merge|NZ_CP040915|2|1028901-1028979|CRISPRCasFinder
CCGCGGTCGATGAAGCGTCAGGCGACGAAGCGTCAGCCGACGACGCGGCGCCCGCGGTCGATGAAGCGTCAGGCGACGA

>NZ_CP040915|2|2|1028901-1028979|CRISPRCasFinder
CCGCGGTCGATGAAGCGTCAGGCGACGA	AGCGTCAGCCGACGACGCGGCGC
CCGCGGTCGATGAAGCGTCAGGCGACGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_168205597.1|1036518_1037502_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270370
NZ_CP040915.1|WP_168205598.1|1037581_1038022_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP040915.1|WP_168205595.1|1023446_1024109_-|PH-domain-containing-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927447.1|1021643_1023344_+|ABC-transporter-family-substrate-binding-protein	unknown	unknown	gnl|CDD|173866
NZ_CP040915.1|WP_139927444.1|1017752_1018736_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP040915.1|WP_139927451.1|1027548_1027962_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927464.1|1040104_1041649_+|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|235730
NZ_CP040915.1|WP_139927443.1|1015852_1017583_+|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224048
NZ_CP040915.1|WP_139927462.1|1038196_1039138_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235546
NZ_CP040915.1|WP_139927446.1|1019628_1021539_+|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224048
NZ_CP040915.1|WP_139927458.1|1034187_1035489_+|citrate-synthase	unknown	unknown	gnl|CDD|99867
NZ_CP040915.1|WP_168205596.1|1032485_1032803_+|ferredoxin-family-protein	unknown	unknown	gnl|CDD|224069
NZ_CP040915.1|WP_139927445.1|1018732_1019632_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224094
NZ_CP040915.1|WP_139927450.1|1026373_1027552_+|GlcNAc-PI-de-N-acetylase	unknown	unknown	gnl|CDD|274584
NZ_CP040915.1|WP_139927452.1|1027954_1028479_+|flavin-reductase	unknown	unknown	gnl|CDD|376575
NZ_CP040915.1|WP_139927463.1|1039134_1040112_+|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|225070
NZ_CP040915.1|WP_139927449.1|1024316_1026230_+|translational-GTPase-TypA	unknown	unknown	gnl|CDD|224138
NZ_CP040915.1|WP_139927459.1|1035617_1036388_+|DUF554-family-protein	unknown	unknown	gnl|CDD|377371
NZ_CP040915.1|WP_139927454.1|1031329_1031845_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP040915.1|WP_168205774.1|1032811_1033942_+|succinyldiaminopimelate-transaminase	unknown	unknown	gnl|CDD|236119

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_168205597.1|1036518_1037502_-|ABC-transporter-substrate-binding-protein	gnl|CDD|270370	cd13652, PBP2_ThiY_THI5_like_1, Putative substrate binding domain of an ABC-type transporter similar to ThiY/THI5; the type 2 periplasmic binding protein fold. This subfamily is phylogenetically similar to ThiY, which is the periplasmic N-formyl-4-amino-5-(aminomethyl)-2-methylpyrimidine (FAMP) binding component of the ABC transport system (ThiXYZ). FAMP is imported into cell by the transporter, where it is then incorporated into the thiamin biosynthetic pathway. The closest structural homologs of ThiY are THI5, which is responsible for the synthesis of 4-amino-5-(hydroxymethyl)-2-methylpyrimidine phosphate (HMP-P) in the thiamin biosynthetic pathway of eukaryotes, and periplasmic binding proteins involved in alkanesulfonate/nitrate and bicarbonate transport. After binding the ligand, they interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ThiY/THI5 proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.5511e-53
NZ_CP040915.1|WP_168205598.1|1037581_1038022_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	9.71539e-16
NZ_CP040915.1|WP_139927447.1|1021643_1023344_+|ABC-transporter-family-substrate-binding-protein	gnl|CDD|173866	cd08501, PBP2_Lpqw, The substrate-binding domain of mycobacterial lipoprotein Lpqw contains type 2 periplasmic binding fold. LpqW is one of key players in synthesis and transport of the unique components of the mycobacterial cell wall which is a complex structure rich in two related lipoglycans, the phosphatidylinositol mannosides (PIMs) and lipoarabinomannans (LAMs). Lpqw is a highly conserved lipoprotein that transport intermediates from a pathway for mature PIMs production into a pathway for LAMs biosynthesis, thus controlling the relative abundance of these two essential components of cell wall. LpqW is thought to have been adapted by the cell-wall biosynthesis machinery of mycobacteria and other closely related pathogens, evolving to play an important role in PIMs/LAMs biosynthesis. Most of periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the LpqW protein. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	4.11575e-131
NZ_CP040915.1|WP_139927444.1|1017752_1018736_+|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	3.09299e-73
NZ_CP040915.1|WP_139927464.1|1040104_1041649_+|long-chain-fatty-acid--CoA-ligase	gnl|CDD|235730	PRK06187, PRK06187, long-chain-fatty-acid--CoA ligase; Validated.	0
NZ_CP040915.1|WP_139927443.1|1015852_1017583_+|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP040915.1|WP_139927462.1|1038196_1039138_+|SDR-family-oxidoreductase	gnl|CDD|235546	PRK05653, fabG, 3-oxoacyl-ACP reductase FabG.	5.59561e-84
NZ_CP040915.1|WP_139927446.1|1019628_1021539_+|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP040915.1|WP_139927458.1|1034187_1035489_+|citrate-synthase	gnl|CDD|99867	cd06114, EcCS_like, Escherichia coli (Ec) citrate synthase (CS) GltA_like. CS catalyzes the condensation of acetyl coenzyme A (AcCoA) and oxalacetate (OAA) to form citrate and coenzyme A (CoA), the first step in the citric acid cycle (TCA or Krebs cycle). The overall CS reaction is thought to proceed through three partial reactions and involves both closed and open conformational forms of the enzyme: a) the carbanion or equivalent is generated from AcCoA by base abstraction of a proton, b) the nucleophilic attack of this carbanion on OAA to generate citryl-CoA, and c) the hydrolysis of citryl-CoA to produce citrate and CoA. There are two types of CSs: type I CS and type II CSs. Type I CSs are found in eukarya, gram-positive bacteria, archaea, and in some gram-negative bacteria and are homodimers with both subunits participating in the active site. Type II CSs are unique to gram-negative bacteria and are homohexamers of identical subunits (approximated as a trimer of dimers). Some type II CSs including EcCS are strongly and specifically inhibited by NADH through an allosteric mechanism. Included in this group is an NADH-insensitive type II Acetobacter acetii CS which has retained many of the residues used by EcCS for NADH binding.	0
NZ_CP040915.1|WP_168205596.1|1032485_1032803_+|ferredoxin-family-protein	gnl|CDD|224069	COG1146, COG1146, Ferredoxin [Energy production and conversion].	5.51848e-11
NZ_CP040915.1|WP_139927445.1|1018732_1019632_+|ABC-transporter-permease-subunit	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.54826e-78
NZ_CP040915.1|WP_139927450.1|1026373_1027552_+|GlcNAc-PI-de-N-acetylase	gnl|CDD|274584	TIGR03445, mycothiol_MshB, N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase. Members of this protein family are N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase, also called 1D-myo-inosityl-2-acetamido-2-deoxy-alpha-D-glucopyranoside deacetylase, the MshB protein of mycothiol biosynthesis in Mycobacterium tuberculosis and related species. [Cellular processes, Detoxification].	1.31935e-47
NZ_CP040915.1|WP_139927452.1|1027954_1028479_+|flavin-reductase	gnl|CDD|376575	pfam01613, Flavin_Reduct, Flavin reductase like domain. This is a flavin reductase family consisting of enzymes known to be flavin reductases as well as various oxidoreductase and monooxygenase components. VlmR is a flavin reductase that functions in a two-component enzyme system to provide isobutylamine N-hydroxylase with reduced flavin and may be involved in the synthesis of valanimycin. SnaC is a flavin reductase that provides reduced flavin for the oxidation of pristinamycin IIB to pristinamycin IIA as catalyzed by SnaA, SnaB heterodimer. This flavin reductase region characterized by enzymes of the family is present in the C-terminus of potential FMN proteins from Synechocystis sp. suggesting it is a flavin reductase domain.	2.52149e-29
NZ_CP040915.1|WP_139927463.1|1039134_1040112_+|amidohydrolase-family-protein	gnl|CDD|225070	COG2159, COG2159, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	8.0055e-72
NZ_CP040915.1|WP_139927449.1|1024316_1026230_+|translational-GTPase-TypA	gnl|CDD|224138	COG1217, TypA, Predicted membrane GTPase involved in stress response [Signal transduction mechanisms].	0
NZ_CP040915.1|WP_139927459.1|1035617_1036388_+|DUF554-family-protein	gnl|CDD|377371	pfam04474, DUF554, Protein of unknown function (DUF554). Family of uncharacterized prokaryotic proteins. Multiple predicted transmembrane regions suggest that the region is membrane associated.	4.32696e-62
NZ_CP040915.1|WP_139927454.1|1031329_1031845_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	9.2937e-19
NZ_CP040915.1|WP_168205774.1|1032811_1033942_+|succinyldiaminopimelate-transaminase	gnl|CDD|236119	PRK07865, PRK07865, N-succinyldiaminopimelate aminotransferase; Reviewed.	0

Protein sequences

>NZ_CP040915.1|WP_139927452.1|1027954_1028479_+|flavin-reductase
MSEASGAAAVTDPEELVERFRATMGRLAGGVTVVAVRSGSSDLAMTATAVASVSLRPPMVLFCVYSDARLREVLDEVETWAISLVDAGALVPAERLAMPGRPAVGQLLGVPHHRGPLSGAALLDGAQGWLECRTAWIKTAGDHDVVVGEVLDATLGPAGGGALVHYLGRFRGLT
>NZ_CP040915.1|WP_139927451.1|1027548_1027962_+|hypothetical-protein
MSSPARPGAAATAAAAVILGVVVAACGTLVHRWEAASLPGGVILALVAVLLGAVVARALADGGGVALYALAAILTSQTMTFFGPGGDVLVTGELLSNVWLLGVPVAAAAAALTPRSWYAGAPAVPARHSGGPHLGDV
>NZ_CP040915.1|WP_139927450.1|1026373_1027552_+|GlcNAc-PI-de-N-acetylase
MTSTQGTRTAELPTGGVLGVFAHPDDETLGAGGLLASAARVGLPVTVVTGNRGERGQVIPRELAHLDGDAPALVHERERELARACAELGVRARVFLDQLPGLAARRPPRFTDSGMVWTRPGLAGPVPDVGPDAQSSVPVEVAARLLAGLVRRTRPQVVITEEPHGGYGHPDHVHAHQVTMRAVEMAADAAEVDDADDPLTGLEPWHVPVVLWAVESEIRMRAALHWLEEKLARAPQFGARGDALATLPAGSELPSLAFPTSKVDLTIDTTAVLPAVVAAMRAHRTQLQNVHLEDLSRSEQRDQPACGWVAVSNGLLLPIMGSASMHLVPGFDRVDELVVEPVHHAYTEPVPVAQRYGLAGTFGLAALDVKNRLAETRGPARLAAFLGGAVLA
>NZ_CP040915.1|WP_139927449.1|1024316_1026230_+|translational-GTPase-TypA
MPVRSDLRNVAIVAHVDHGKTTLVDAMLWQSGAFGEHQHVDERAMDSGDLEREKGITILAKNTAVHYRGPAALKAGLEDGLTINVVDTPGHADFGGEVERALSMVDGVVLLVDASEGPLPQTRFVLRKALAAKLPVVLLVNKVDRPDSRIDAVVTEAQDLLLGLASDLADEVPDLDLDAILDVPVVYASGKARRASLNRPADGTLPDHEDLEPLFATIIEKIPAPTYEEGAPLQAHVTNLDASPFLGRIALLRIHNGELRKGQTVAWARHDGTMKNVRISELLRTEALDRVPTERAFAGDIVAVAGIEDITIGESLVDADDPRPLPLIQIDDPAISMTIGINTSPLAGRVKGHKLTARQVKDRLDRELVGNVSLKVLPTDRPDAWEVQGRGELALAILVEQMRREGFELTVGKPQVVTKIIDGKRHEPMERQTIDVPEEYLGTVTQLMAARKGRMETMSNHGTGWVRMEFVVPARGLIGFRTRFLTETRGTGIASSISEGYEPWQGEIEMRNTGSMVADRAGAVTPFAMIKLQERGSFFVEPTSEVYEGQVVGENPRNEDMDVNITKEKQLTNMRSSTADNFESLVPPRKLTLEESLEFAAEDECVEVTPEAVRIRKVILDANERYKSASRNRRAAG
>NZ_CP040915.1|WP_168205595.1|1023446_1024109_-|PH-domain-containing-protein
MGPTVVFRPDSSRVYAVICWVVAAAVLVAFAVNGGVGELVRYGALPLAVAAFGWAVFWRPFVEVGPDGVTLANVVRTVVVPWGAIDAVETRWGVRLRTAAGAFGAWAAPARAGFGRSRSLREAENLPDRLFRGSGTVSASGDAAAVGSVIEDRLGRRDRLARTGARGTAQVGLDGSGQAGPRQTGRAGSDPAPRARVNIPEVLALGVTVALAVVSLVVPV
>NZ_CP040915.1|WP_139927447.1|1021643_1023344_+|ABC-transporter-family-substrate-binding-protein
MRRSTAALAAGAALALALAGCAGSAGPDGTPSPTPSATASASGPDVADVNATPRENLADGGVLRQAVGALPTQWNPLHVGGTAETFTQVRGPMSVTNFDTDAEGVPTPNPNFVTSVEESSTDGRQVVTLHLNPDAVWNNGEPITWEDYAATVAACNGQQPEFQCATGLFAAVEEVAQGETEFDVVVAFASPFPDWPALLGTVLPAAGVADAATFNTGWLDHPEDWFTGPFTLADLDTDQQVATLVPNERWWGPEPVLDEIEYRAVAPEATATAFANNEIDVFDIGADPNAYQLARQVPGAEVRQAGGVDWRQFTFNSTAGHLTDQAVRQAIVRALDRQAIAAASLAGLPEDLQRPLNNHIFMAGQDGYEDNAGDYAHDPARAVTELDAAGWVLDEVTGVRERNGEPLTVRFTVFTGIPASETEGQLVQAQLREVGIDVQLDHVPEAAFNDTLNNGDFEIIAFSWFGSAFPLLGLGNIYGDPATTPMNYAHLATPGLDELIGQIATETDHATRLDLADQADELIWDAVHTLPLYQRPQLVAAVSELANIGAPGLSTTRPEDWGFVAE
>NZ_CP040915.1|WP_139927446.1|1019628_1021539_+|dipeptide-ABC-transporter-ATP-binding-protein
MSEPVLELRDLHVHLRASDGEVHAVRGIDLAVREGEVLAVVGASGSGKSATAMAVMGLLPASARVSGSVRLDGAELLGRSDAELSRVRGARIGMVFQDAALTPVYPVGEQVAEALHAHRRLGRAAARARAVELLELVGIDRPAARAHAFPHELSGGMRQRVAIAIAIANDPDVLVADEPTSALDVTVQAQILDVLRTARDETGAALVLISHDLGVVAGLADRVAVLDAGQVVEVGDVETIFARPAAPLTRALLDAVAWPRATAPASPMAAAPPAETAAPPDRAEVLRVTDLHRHFPLTRGTLLRRRVGTVRAVDGVSLTVRAGEVLALVGESGSGKTTTVRSVLELTTPERGAVVVLGTDVAGLDRAGRRRLRRGVQVVLQDPDAALDPRLPVTDLVAEPLLADGRTGSAVSRRVAELLGLVGLDPALGDRFPRHLSGGQRQRVAIARALALEPRLMVLDEPVSALDAPVRAEILDLLGDLRDRLSLSYLLVSHDLAAVRRLADRVAVMHLGRVVESGDATQVFTRPAHPYTRVLLSAMPVADPVLERSRQRTVLVGDLASPADAPSGCRFRTRCPLYRTLDPTAQERCRDEDQPLRIVGGQRAGGHRPPTRQPLTHQAACHVVTNTSPPAAPWRG
>NZ_CP040915.1|WP_139927445.1|1018732_1019632_+|ABC-transporter-permease-subunit
MTTSVLATLPTPVGPGARFRLVARRFRRDRAAVAGMAGLALLVILSLVGPQLAPWGYAEIDSTAFLAAPDASHWWGTTQAGRDVFALTVEGLRTSLLVGLGAGLLQTVIAAAVGTVAAYRGGWLDRVATWVIDLLLVVPSFFLVAILSVRAGGEAGSVALLVLLLGGLGWMLSARVVRAMTLSLRELDYVTAARYMNVPTRTIITRHILPNLSSLLVVDATLAVAAAVLAETALSFFGFGVQAPGTSLGTLIAEGQRTATTYPWIFLAPAGTLVALLVSVNLVGDGLRDALDPSQGGRA
>NZ_CP040915.1|WP_139927444.1|1017752_1018736_+|ABC-transporter-permease-subunit
MFRYLARRLAGYAVLLFVAVSLTYVLAATALDPRSLYELRNPPLEPAAIEASLAAYNLSDAVPLAERYRTWLTDIVADWDWGRTPAGASVNEQIGGRIWVSLRLVTLGSVLGTLAGVALGTWSAVRQHKAGDRLVTVAALVVISTPTLVLAVVLQIVAVQVNRATGVQLFEFLGESGAHGGGALAALGDRLQHLVLPTLTLAAGQAAFFSRVQRGLVLDTLGASYVRAARAKGLRRSVAVRRHALRTALVPTGTYFAYTVATLVLGAAFVEAVYGWHGMGIYGVRAIAGQDVHATVAVAAFGATCVLAGALLADLLTAALDPRVRTR
>NZ_CP040915.1|WP_139927443.1|1015852_1017583_+|dipeptide-ABC-transporter-ATP-binding-protein
MTKTNDVVAPVTAGLDPHEALLEIRDLEVAFKSSTGMVPAVRGANLTVYPGQAVAIVGESGSGKSTTAHAIIDLLPGTGRVTGGSIKFLGRDITNPSRKAIEGLRGKEIGLVPQDPMSNLNPVWKIGSQVKEALTANGMDRAEAKDRVNEVLSQAGLPDAERRAKQYPHEFSGGMRQRALIAIGLAARPKLLIADEPTSALDVTVQRQILDHLEHLTKELGTAVLFITHDLGLAAERAEHLVVMHRGRVVESGPARQILTAPQHPYTQRLVASAPSLASRRIQSAKARGEESTELLADAEAAAAAPNIVEVERLTKEFHLRGGVPGAGKSFKAVDDVSFSIPRGSTMALVGESGSGKSTVANIMLNLLEPTEGRVVFEGTEVGTLGKRELFNFRRQVQPIFQNPYGSLDPMYSIFRTIEEPLRVHGVGDKKSRAAKVAELLEMVALPRSTMRRYPNELSGGQRQRVAIARALALEPKVIVCDEAVSALDVLVQAQVLTLLNDLQAELGLTYLFITHDLAVVRQIADRVAVMEKGKIVEQATTDEVFENPRQAYTRELLAAIPGASLEMELAGPEQL
>NZ_CP040915.1|WP_139927454.1|1031329_1031845_+|GNAT-family-N-acetyltransferase
MDPIRRARPDDVPAVLQLVRDLAAYEREPDAVRLTEFGLHAALFGEEPAVFAHVAEADGEILGFALWFRNFSTWEGVHGIYLEDLYVRPEARGRGYGKALLQTLARHAVAQGYARMEWSVLDWNAPSIEFYRSLGARPQEEWSVFRLTGEALAEVGAPAAVTTAAEAPVSR
>NZ_CP040915.1|WP_168205596.1|1032485_1032803_+|ferredoxin-family-protein
MTYVIAQPCVDVKDRACVDECPVDCIYEGARMLYIHPDECVDCGACEPVCPVEAIYYEDDTPQIWADYYRANVEFFNDLGSPGGAAKMGVIDKDDPMIAALPPQA
>NZ_CP040915.1|WP_168205774.1|1032811_1033942_+|succinyldiaminopimelate-transaminase
MHGRALPDFPWDSLAPAKTRAAAHPGGIVDLSVGTPVDPTPAVAQDALRAAADAPGYPTTVGTLALREAVVAWFARRRAVPGLGVDQVLPTMGSKEMVALLPALLGLGEGDVVVHPRAAYPTYDVGARLAGATPVPVDDDPATWPDARLVWLNSPGNPHGHVLGVDQLAAVVAWARERGAVVASDECYAELPWAEPWASDGVPSLLDPRVTGGDHRGLLVLYSLSKQSNLAGYRAAFVAGDPALIGPLTEVRKHSGMIVPAPVQAAMAAVLGDGAHVDAQRERYRARRAVLLGAVEQAGLELDPATVAGLYLWVRAAGATTASWELVDALSHRGILVAPGSFYGGDGGGYVRMALTATDERIDEAARRLREGGPLV
>NZ_CP040915.1|WP_139927458.1|1034187_1035489_+|citrate-synthase
MSIAEQNAAATFQVDGKALQFQRVDAVEGNDGINISSLLKETGLVTLDPGFMNTASTTSAITYIDGDEGILRYRGYPIDQLAKGSTFLEVAYLLIYGELPDAETLEAVTRRIKRHTILHEDFKAFFTAFPANGHPMAILQSGISALATYYQHTLDPKDPYQIELSTVLLMAKVPTMIASIAKRATGLPLLYPDASKSYIEDFIRMTFGLPYQRHDVDPAITRALEMLLILHADHEQNCSTSTVRMVGSSHANIYASVAAGVGALSGPLHGGANEAVLEMLNRIHTGGDTVDQFMTRVKNKEDGVRLMGFGHRVYKNYDPRAAIVKEAAHDVLQRLGKNDQLLDIAMGLEEIALHDEYFIERKLYPNVDFYTGLIYKAMGFPTQMFTPLFALGRLPGWIAQYREMIADPTTKIGRPRQVYTGQPERQYQPTDKR
>NZ_CP040915.1|WP_139927459.1|1035617_1036388_+|DUF554-family-protein
MDGFPGLGTLINVGAIVIGSTVGMAVGHRLREATRTVITDGLGLITLLLAASMCVSIADPALVAAVGPGVPVLVVLGAILIGGLTGSVLRIEQGLEGAAAQLQAWAFRRRVGGPGDAHVARERFVEGWLTASLVFCVGPLAILGSLSDGMGNGIEQLALKSVLDAFAALAFAATFGFGVVLSAASVAVVQGGLTLVGVLLGSVVPDAHIAALTVTGGLLLGGIGLRLLNIRNIAVGDMLPALVVAPMLTQAVVLLR
>NZ_CP040915.1|WP_168205597.1|1036518_1037502_-|ABC-transporter-substrate-binding-protein
MRTRMCVLTAGVLLALTACSSGGSDAPADSTTGSGESGAATETTEIQMGVLPIVPSAALQLGIDEGIFADHGFDVSLETGQGGAALLPAVMSGQLQFAISNPLSIMLAQEQGLDIRMVTGYSHSNAEGDDVTSVWAKADSGIASPADLAGKTVAVNTLKTMGEISIKEIVSKAGGDPDSINFVELGFPDMPAALESGNIDAAWVPEPFQTIFKDSGANLVAYNYQETMPGVPTMSVITAGPLAESDPDMVQEFVAAVDEVTTFAEDNPDKVRATLTTFLDMDEELANKVLVEHFGAQMNEDSLQALSDLSVKYGLLKEPVDMATFMP
>NZ_CP040915.1|WP_168205598.1|1037581_1038022_-|MarR-family-transcriptional-regulator
MRAPENIGLLLSLASARGVASANVALGPVELNSRSYSLLEQLAGTDGVSQRALADAIRLDPSQIVAMIDGLERRGLAERRPNPADRRQKSVVITGPGRTLFHRARALVESSVDEVLAGLDDLERETLRGLLQRIVRHDAARLENAS
>NZ_CP040915.1|WP_139927462.1|1038196_1039138_+|SDR-family-oxidoreductase
MSLTGKVAIVTGSGRGLGLAYAQELARHGARVVVNDVDQQVADDAVAAITAAGGEAVGVVAPVGPTETAKALVAAAVEHFGRLDILVTNAGVLRDTVLWKMSDDDFDTVINVHLRGTFTCVREAATYLREQGEGGRIICIGSPTGQRGNFGQTNYAAAKAGIVGMVRTWALELARANITANAVIPVAATAMTETVPFFKDFVDAAARGEQMPPFARRVLGFGTPDDVAGVVAFLASDAAAGINGQAVGVGGDRLAVWSHPQEVTTAFTDGGWSYEALTEDWESLFGGALQSVGQPMPAPPARAGTEPGEKVRS
>NZ_CP040915.1|WP_139927463.1|1039134_1040112_+|amidohydrolase-family-protein
MTYTSALDVAALTAIDTHVHVEKDTHGHLSLPGEVLDAAAKYFKAPTDRLTIDETADYYRERSMAAVVFTVDATTKLGHAPNSTEEIVAGAARNNDVLIPFGSVDPHAADAVDRVRRQIEDLGVRGFKFHPSLQDFDPSDERYFPLYEVIAAAGLPAIFHTGQTGIGARLPGGFGLKLGLSNPMLLDVVAATFPGLTIIMAHPSVPWQDEAISVATHKGNVYIDLSGWSPKYFPPALVKQANSVLQDKVLFGSDFPLLTPERWMRDFAALELKDEVRPKILKDNAVRVLGLGGPSSPTAPNPATQAAPNPATQAAPSSPRGAARA
>NZ_CP040915.1|WP_139927464.1|1040104_1041649_+|long-chain-fatty-acid--CoA-ligase
MRDQGIGSWPARRCKNGAHRTALVHGERTDTYADVERRTRQLANALRADGVGRGDRVAFVGFNHPALLETFFAVGQLGAIWVIINARLTAPEVEYILADSGATVVVYGPEHAGHAAKLAHLPGVRTWVAVEPDDGAADAPSSALSYEAFLAAGATDVIDEPVSWDDPAMIMYTSGTTGRPKGAVHTHGSLHMQYFNVLVDLDVARDDVTLAVAPMFHVAGLNMLTLPTFLKGGKIIIQPGFKPDRVLATIAAEKVTSVFAVPAMMDALASHPDFAATDLSSLTNVVVGGSPLPDRMLRTWAARGIGIQQGFGMTETAPGIYLLTAEDSLRKPSSAGRNHFFTEGRVVRLDGTDVAPGENGEVIGQGPNVMQGYWNNSGATAEAIVDGWYHTGDVATVDEDGYIYIRDRLKDMYISGGENVYPAEVENALLDLPGVAEAAVIGVPDPRWGEVGHAYVVAAEGATLTAEDVVARLTERLAKYKVPKEVVFVDELPRTATGKLQKHLIRTRFQESAL

Crispr_ID: NZ_CP040915_4

• CRISPR_ID: NZ_CP040915_4
• CRISPR_location: 1057785-1057894
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_4

Consensus_repeat	Method
CGACATCAACGACTCGTTCAACGAC	CRISPRCasFinder

spacers of NZ_CP040915_4

>4.1|1057810|59|NZ_CP040915|CRISPRCasFinder
AACTTCTCGAACAACTTCACCGACGACGACGTCCTCGACATCGACGACCAGGACTTCGT

CRISPR arrays and Neighbor proteins around NZ_CP040915_4

CRISPR arrays

The CRISPR arrays of NZ_CP040915_4

>merge|NZ_CP040915|4|1057785-1057894|CRISPRCasFinder
CGTCATCGAGGACTCCTTCGACGACAACTTCTCGAACAACTTCACCGACGACGACGTCCTCGACATCGACGACCAGGACTTCGTGGACGTCGACAACACGGCCAACGACA

>NZ_CP040915|4|4|1057785-1057894|CRISPRCasFinder
CGTCATCGAGGACTCCTTCGACGAC	AACTTCTCGAACAACTTCACCGACGACGACGTCCTCGACATCGACGACCAGGACTTCGT
GGACGTCGACAACACGGCCAACGACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	unknown	unknown	gnl|CDD|178901
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	unknown	unknown	gnl|CDD|377577
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	unknown	unknown	gnl|CDD|320679
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	unknown	unknown	gnl|CDD|227136
NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173840
NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein	unknown	unknown	gnl|CDD|237171
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	unknown	unknown	gnl|CDD|381681
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	unknown	unknown	gnl|CDD|274635
NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	unknown	unknown	gnl|CDD|212667
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	unknown	unknown	gnl|CDD|379386
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239217
NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	unknown	unknown	gnl|CDD|227111

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	gnl|CDD|178901	PRK00148, PRK00148, Maf-like protein; Reviewed.	7.51248e-84
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	0
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	gnl|CDD|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	3.89009e-59
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	gnl|CDD|227136	COG4799, COG4799, Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) [Lipid metabolism].	0
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	gnl|CDD|379386	pfam13822, ACC_epsilon, Acyl-CoA carboxylase epsilon subunit. This family includes the epsilon subunits of propionyl-CoA carboxylase, EC:6.4.1.3, and acetyl-CoA carboxylase, EC:6.4.1.2. These enzymes are involved in the biosynthesis of long-chain fatty acids. The epsilon subunit is necessary for an efficient interaction between the alpha and beta subunits of these enzymes.	5.74672e-06
NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase	gnl|CDD|173840	cd01151, GCD, Glutaryl-CoA dehydrogenase. Glutaryl-CoA dehydrogenase (GCD). GCD is an acyl-CoA dehydrogenase, which catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and carbon dioxide in the catabolism of lysine, hydroxylysine, and tryptophan. It uses electron transfer flavoprotein (ETF) as an electron acceptor. GCD is a homotetramer. GCD deficiency leads to a severe neurological disorder in humans.	2.76489e-109
NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein	gnl|CDD|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	5.73429e-08
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	1.57556e-15
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.26291e-19
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.0804e-15
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.46344e-23
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	gnl|CDD|274635	TIGR03535, DapD_actino, 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. This enzyme is part of the diaminopimelate pathway of lysine biosynthesis. This model represents a clade of the enzyme specific to Actinobacteria. Alternate name: tetrahydrodipicolinate N-succinyltransferase.	1.01875e-171
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	gnl|CDD|381681	cd10031, UDG-F5_TTUDGB_like, Uracil DNA glycosylase family 5, includes Thermotoga maritima TTUDGB and similar proteins. Uracil DNA glycosylase family 5 includes Thermus thermophilus HB8 TTUDGB (also called UDGb) which is not only a UDG acting on double-stranded uracil-containing DNA, but also a hypoxanthine DNA glycosylase acting on double-stranded hypoxanthine-containing DNA (except for the C/I base pair), as well as a xanthine DNA glycosylase acting on both, double-stranded and single-stranded xanthine-containing DNA. TTUDGB also excises thymine from G:T mismatched DNA, and removes analogs of uracil from DNA, including 5-hydroxymethyluracil (hmU) and 5-fluorouracil (fU). This subfamily also contains Bradyrhizobium diazoefficiens family 5 homolog Blr5068 (UdgB) which has been found to efficiently excise uracil from ssDNA and dsDNA. Uracil-DNA glycosylases (UDGs) initiate repair of uracils in DNA. Similar to family 4 UDGs, members of this family possess four conserved cysteine residues required to coordinate the [4Fe-4S] iron-sulfur cluster. Uracil in DNA can arise as a result of mis-incorporation of dUMP residues by DNA polymerase or via deamination of cytosine. Uracil in DNA mispaired with guanine is one of the major pro-mutagenic events, causing G:C->A:T mutations. Thus, UDG is an essential enzyme for maintaining the integrity of genetic information. UDGs have been classified into various families on the basis of their substrate specificity, conserved motifs, and structural similarities. Although these families demonstrate different substrate specificities, often the function of one enzyme can be complemented by the other.	1.31618e-105
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	gnl|CDD|212667	cd10170, HSP70_NBD, Nucleotide-binding domain of the HSP70 family. HSP70 (70-kDa heat shock protein) family chaperones assist in protein folding and assembly and can direct incompetent "client" proteins towards degradation. Typically, HSP70s have a nucleotide-binding domain (NBD) and a substrate-binding domain (SBD). The nucleotide sits in a deep cleft formed between the two lobes of the NBD. The two subdomains of each lobe change conformation between ATP-bound, ADP-bound, and nucleotide-free states. ATP binding opens up the substrate-binding site; substrate-binding increases the rate of ATP hydrolysis. HSP70 chaperone activity is regulated by various co-chaperones: J-domain proteins and nucleotide exchange factors (NEFs). Some HSP70 family members are not chaperones but instead, function as NEFs to remove ADP from their HSP70 chaperone partners during the ATP hydrolysis cycle, some may function as both chaperones and NEFs.	1.18947e-94
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	gnl|CDD|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	3.09539e-11
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	gnl|CDD|227111	COG4770, COG4770, Acetyl/propionyl-CoA carboxylase, alpha subunit [Lipid metabolism].	0

Protein sequences

>NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator
MVAATPTHQVRSRQRALLEAIDVSGRPLNGVASRLARSGIEDPRVAEALVAQGDTLLPRDPAKAFEVYSQAVAAGADHTALAARRAQAAALSGNLDPAGRLVDELLSLPEPPDLGRAVDVAAEVWSRRGMLSRSADVYRWLGPDRIGASAPLAAIALVGCGDRAGMDDMLAAAGPPTSPTLLAAVPTLVCEGLRETLDSASTNAMGSLVRASDMMTASGSTLPMPMNPAALAALVALHLGELAVAESVTEDALAGNQGGAGCRPRLLLMRAWTAMLRDRPDHARAAITEARSAGEVLSPRDELFLRALEVGLARRTDDPPGLVQAWGRARESILHFPVDLFTLLPLGELLVAAARLRDSARIEGHVAEAWALLGRLGDPPLWTVPLHWAEVHAAILAERPGQLGPHAAALVRASGQSHFAAVLAAAGRVWVSVLAGDVDVEAVEIAARGLASVGLTWDGSRLAGHAAARAPERKDMARLLARARDLHPAAALAPEQAPTAPPGSNRSGTLLDDSGLSPREREIAAQVLAGRTYREIGDAIYISPRTVEHHVARIRRRLGASSRSELLARMRIALGEESWTS
>NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein
MTYSVGVDIGTSFVAAAITRIVDGRPQAPQPLHLGARSTATPSVMYFGDDGQVLVGDAAERRGTTDPDRVVRESKRRIGDSVPVVVGDLLVAPEDIYATMVRWVVDRADEQEGAPPDRVAVAHPVGWGAYKTGLVREALAGVGLGEVELISEPEAAALHYASFERVEVGSTIAVYDLGGGTFDVAILRKAETDTFDVLGRPEGIERLGGADFDEAVFRHVTAGLGEGFTSLDRTDPGVLVALSRMRRECTEAKEALSSDSETVVPVLLPGMQTQVRLVRSEFEELIAASVRETVASVEQALRTAQVEPEDLTAVLLIGGSSRVPLVAQLLSAELGRPIAVDADPKASICLGASLAAAYPGAIEGTAVLLGDDDVTVAPARAQAGDGVAPVTEPPSPAGAALAPAATAFVANAPHQHIGSRRGIKIAAIAGLVASITVFTTVAGQTPEVQELIKSSLRVSEAQAGTPAADGGEAVAAGEDGRGGAGGSGEGASSDRSGVARLNTVAPKPGDPTGKPKPTPTDEASTKVSATGSPTTGVPGTTSTGGKTTPGTNTPGGTATGDGSGTGGAPTGTPDGAGTPTTDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTEPPPEPEPTATATATATATEESTPPQDPPPPADTPPAEEPPATGAAITVPADPVLG
>NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf
MTTLLLASASPARLSTLRAAGLDPLVAASSVDEAKLLATATTEADRAGSAPVPPADQVLLLARAKAHDVREHPTLAREADVVLGCDSMLELEGEVLGKPTDAADAVVRWQRMRGRTGVLHTGHCLLDRDGREASATSSTVVHFADLTDAEVDAYVATGEPLWVAGAFTVDGLGGPFVAGIEGDYHGVVGVSLPLLRVLLAELGVAITDLWRPAAD
>NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase
MATVSTAPDLRPHPVTGRLFPSPVPPGTGWPEDPADAGTPVATTVPAVVDLARAAADVGELDARVSVCRACPRLVAWRESVATTGRRASFADQPYWGRPGPGVGDPAPQVLVVGLAPAANGTNRTGRMFTGDRSGDWIYAALYRAGYASQPDSWAAGDGLKLAGARIVAAVRCAPPANKPTPEERRTCGHWLDRDLELAAPGLRSMLALGAIGWDAALASARRLGWTVPRPKPRFGHGAQTELVAADGHPIRLLGSYHVSQQNTFTGRLTEAMLDAVIARL
>NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein
MTSTSSQLSPRGLTKVLIANRGEIAVRVARACADAGVATVAVYADSDRDALHVKLSDEAFALHGQRAAETYLDAGKILDVARRSGADAVHPGYGFLSENAGFAQAVLDAGLIWIGPPPAAIEALGDKVTARHIAQKVGAPLVPGTPDPVSGAEEVLAFADAHGLPIAIKAAFGGGGRGLKVARTREEIPELYESAVREAVAAFGRGECFVERFLDRPRHVETQCLADAAGNVVVVSTRDCSLQRRHQKLVEEAPAPFLTPAQEQTLVHASQAILREAGYVGAGTCEFLVGQDGTISFLEVNTRLQVEHPVTEEVTGIDLVREQLRLAAGEDLGYTEVATRGHAIELRINGEDPASGFMPAPGTISSLSWPSGPGVRVDSGVVAGDTISGAFDSMLAKIIITGATRTQAIERARRALRETEIVGLPTVVPFHRSVLTEPDFTADDGASSFGVHTTWIETDYAEHLRSLPSTRPAPAVAAPAEEPAEATERVIVEVGGKRLEVVIPAGLGISTGPRGAARRPVRRTVGRSSGTGGTNGAALTSPMQGTIVKVAVGDGEVVAQGDLVVVLEAMKMEQPLVAHRAGRVSGMAAAVGRNVATGAVICQIEPVEQAAPDAG
>NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein
MTASASRPPDARVHRQPGDGWVECSCGRRHWGLNGAAGLLLWRTGPAGPQLVLQHRALWSHHGGTWGLPGGALSDGETPVDGAVREAREEAGVVPAGLQVTAARALVHPDWAYTTVLAQATAPFEPAVTDPESLEVRWVDLASIEGFDLLPAFGDALPELRTMLRRLVLVVDAANVVGSRPDGWWADRAGATVRLRDHLAALARDGLDAVAVDLPGQRWYPEVVLVTEGAARGVDPTDGVRVVTAHGSGDDAVVQTVTAVLGATGDGVTDVAVATADRELSARVAALGARTLGPLLVRH
>NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase
MTERTAWAFGLATITDTGDTLEAWYPAPTLGAPPQDAAAPAELSAATSVDASRLVRTEVVRTEIDLDAAPASVADAYLRLHLLSHTLVQPNSINLDGIFGVLPTVVWTSAGPCAVEGFEATRARLRARGVLTVYGVDKFPRMVDYVVPAGVRIADGDRVRLGAHLAPGTTVMHEGFVNFNAGTLGRSMVEGRISQGVVVADGADVGGGASIMGTLSGGGKRVISVGPRSLLGANAGLGISLGADCVVEAGLYLTAGTKVSVIIGGGARPRHGQLDEPAVVSARDLSGRDNLLFRRNSLSGAVEAISRSGTGAELNAALHA
>NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein
MGCTGGAVLALGALGVAITGVVLALNTFVHSPASGTCTVALADGGVQRLDADQADNAALFAANAAHRDLPARAVTIAIATALQESKMRNIDYGDRDSVGLFQQRPSQGWGTVEQIMDPVYSTNAFYDVLVTVQGWESQEITDAAQRVQRSGFPLAYAQHEDRGRAFASALSGYSPASLSCHLDPVVEAPDGVGAPGSAGDGESTPTAVVEGTASAGPIAGATPPARLATIQQRLTRDFVDISATVVPAGVLQVDATSLPAGLDPAPARRGWAVAQWAVATASQTGARVVAVDGQVWVRDDGDDAAWLPLAEAGLPAALHDATASAAPGAVLIG
>NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein
MNTNEGPELILVRDLTALGRDPRSTQRASRSRALTRVRRGAYADARAWATATNSERHRLFVLSTMAGMRTPPVLSHESAAVLLGIPLMGPPPEKVHVAGDSASGGRSSACIQRHVVRPMPAITLVDGVAVTSAARTVVDLARSRPFTAGLVAADYVLRVGLVARAHLDEALDEVAGQRGARRARAVIDRADARAESVGESLSRAQMHLLGVPIPELQHVFYDADGFIGRTDFWWVEERKVGEFDGRIKYQPPERSGGLPPEKVVWREKRREDRLRRQIEGVVRWVWTEALNTSGFGRLLAGAGIYPVRPGVRP
>NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase
MTTTDGAAVTTGPRATAGAAVTTQSSAADLYARSDQYGYANLLTDDERAVLATLRTFLETQAAPLVADHWERGEFPTQLLGPLAGLDLMAPPSLTGGGARPRQLFEGFRVFELARTDASLATYFNGQASLFRSNVLLGGSAEQVARWDPLITRFEMTGVFALTEPEHGSDIAGGLATTARREGDTWVIDGAKRWIGSAAYSDYLTVVARDEADSKAKAFLVRTDAPGVELRKIGGKIALRMVNNADITLTGVRVSEEYRLQRVNSFADIAAMLRAMRAGVAWIATGVQAGAYEAALRYVLERHQFGRPIGGFQLVQDKLVRMLGNLTASLGMVVRLAQQQDASVYRDEDSALAKAWVSARMRETVALAREVAGGEGITLATDVARFFADAEAVYTYEGTNEINTLVVGRAITGLSAFTR
>NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein
MTNIATSLLDFILGLLRDPEAAEKFKDDPEGELHKAGLDDVSSDDVDAVLPVVLDYAPVRVDSSFDRNYDTGGNSSWAGQSGGRDGRDGRDGRDDDHGSGGGRDHGGRDDDHGHGGRGDDDRDDDHGRDHDRGGRGDDDHSHAVQQITHVVNNYSYTSTVDDRDTITDQSVNQNIWAKGDVNQWFDNDAIVASGAGAIAAGDDVSVDDSTDNSTNVLAHDSNVEIGNTDVDINDSFNDDHSTDNSDHSTNVINDSFNDNSDNSTNLDVDIDDSFNDESVDVDVDVDDSFNEDNDGVDIEEVDVDDSFNQDNDGIDVEEVDVDVDNSNQGNTTISDNEVGNTEVSDNVVIADNEVGNTEISDNVVIEDSFDDNFSDNFTDDDFVDYDDQDVVDVDSSLNDNDIDAP
>NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA
MADLVKLVEQTIALVRDGDRADLSRRLEHTRQRLLDPSIRVIVVGEFKQGKSMLINALVGAPVCPVDDDIATAVPTVVRHGAAPSAVVLVPDPGGTDAEPTVQRRPVPLEELPAYVGEAGNPGNVKGLLGAEVTLPRAILAGGLAIIDSPGVGGLDSAHALTTLTALPTADAMLLVSDASQEYTEPEVAFLRQSMRVCPNVAGVLSKTDLYPQWRQVAQIDRGHLAKVDEEIPLFPVSSVLRLQAGRAKSQELNEESGFPGLIGYLRREIVGQAERLQRRSVAQDLRSTAEHLRLSLSSELAALENPEGTPQLLAELEVAKEHADEQRKKSARWQVTLNDGVADLISDMEFDLRDRLRAVQRDAEAAIDAGDPGPVWDQFTDWLEQRVAATVSETFLWTSERSQWLAEQVGALFAQDELRLPVLRVDDTDDVLDPVPLVPDLDAGHLSVTQKVLIGMRGSYGGVLMFGLLTGIAGMALINPISVAAGVLLGGKVYREDKEARLRRRQGEAKSIVRRQIDDVSFQVGKQLRDRLRIVQRTIRDHFTEIAEEHHRSLSDSVVAAQRAASIFSAERDQRIAVLKIDLNRVDALARKADALETADAEAPEPRSARAGRAGTPSRVGRPRGGAVVAEA
>NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein
MSTEGGVRLLLREALEVYADDPVAATSLHGWASRLDGPLRVAIAGMVKAGKSTLLNAILGEELAPTDTGECTRVVTWYRHGATPRVTLYPRDGEPRQLPLRRVEGRLRLDLGGTPAEEVARLVVDWPTAGLRDLTLIDTPGIASLSTDVSARATAFLTPEDSPSEADAVVYLMRHMHGSDIHFLESFRDAEAGRSGTVNALAVLSRADEVGAGRLDSMISARDVARRYREDPSLRPLALSVVPIAGLLAQSARTLRQSEFAALRELAELGREERERLLLSADRFTRAEITPAVDVTMRAALVERLGLFGLRLALVLIRSGLDDPTDLARELARRSGLGELQRLIDGQFQARSAQLKARTALVGLETLLRTRPRPGTERLATELERIQAGAHEFRELRLLGTARTVGLGLPRDLEAEAERLVGGRGVAPARRLNLADGASDAKIRAAALESLRRWRALAENPLTDRSTAGACEVVARSCEALVVAAQPVAGPTTRPQLRPEPARGGG
>NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein
MTYQADAPVHREVEAPGALRTSRTLWLLSFVAGLVAVGFSWLNRDDGKQRLLETVTDLAPGRDAATLEALANLVFWGSLGAIALVVVLEALLLRTMMRRRAWPRVAAFFVLVVHAAVMVLAEAYLAAPGGAGAAVRWPLLIQLGLAVVAWIVSLSPAASRWFRA
>NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein
MRRIALDPLEATSLGLPGHDHEMPDLSPAGLAARTDLDRATLAELEAVAPVDGVDRVTHAAMRERLGVAVELADAGELTRELNVIASPVQAVREVFDLMPTATAADWETIAERLRAVPAALDGYQDSLLAARGAGHVAALRQVEACLKQADELADADTSFFTTFTAGAQPDGEAPHRALAAELEAGARDARQAYADLARMLGEELAPDAPELDAVGRERYGLWSRYFLGAVVDLDETYAWGQEDLARVVAEQQAVAEELYGPGTGIREAMDRLDKDPDRMLHGTPALREWMQATSDEAVAALTDAQFDIPEPVRRLECMIAPTQSGGIYYTGPSADFSRPGRMWWSVPAGVTDFATWREKTTVYHEGVPGHHLQIGQTVYRSGLLNMWRRMASWVSGHGEGWALYAERLMADLGFLDDPGDRMGMLDGQRLRAARVVLDIGVHLGKPAPDEWGGGTWDAAKAWPFLKANANMAEGFLAFELDRYLGWPGQAPAYKIGQRLWEEIRDDAGTAARRDGGELDLKAFHRRALDIGSVGLDVLREALV
>NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein
MGRWSRPLAAAFVEWLGAPDGLEWLDVGCGTGAVTAAIVTGAAPSAVLAIDPSPGFVATARRLTASPLARFTVGDAATLPMGDDAVDRCVSGLVVNFLPDASAAVAEMRRVTRRGGWVAAYVWDYAGGMELLREFWAAAVTVDPGAAQMDERHRFPLCAPGPLGELWRSAGLDGVESRPLTVSTHFPDFDDLWAPFLGGQGPAPAYVGSLTPERRPALARELRRRLHPSADGAIELTARAWAVRGRRR
>NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon
MTSPAVRVLRGRPDEVELAALVAGIVAARGRADELGGLPDEAAECVRSRWSERARVLGMATAPDAGAWRWSLHP
>NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta
MTDSSIDLSAPVAGASPAGDSPATPPTAVPAQPPTTAAKVADLAAREQNLTDAAATAVEKQHKRGKKSARERIEALLDPGSFTELDAFATHRSSNFGLDKKRIPGDGVVTGYGTVDGRQVCIYSQDFTVFGGSLGEVHGQKITKVMDMALTTGVPLIGISDGGGARIQEGVAALTQFAEIFRRNVAASGVIPQISLILGPSAGGAVYSPALTDFIVMAEGTSNMFITGPDVIKAVTGEEVGFEELGGAATHNQRSGVAHYQAADEDDAVDYVRALLSYLPSNNLSEPPSWPVSADEAEAALEVTDTDRELDTLVPDSDNQPYDMRVVVEHVLDDHEMLEVQPGYAPNMITAFGHVEGRPVGVVANQPQQMAGTLDINAAEKAARFVRTCDAFNIPVLTFVDVPGFLPGTDQEWNGIIRRGAKLIYAYAEATVPLVTLITRKAYGGAYIVMGSKKLGADVNLAWPTAQIAVMGSGGAVNILQRGALKKVAEEGGDVEAERARLVAEYEETLVNPWEAAERGFVDAVITPADTRVQVVKALRALRTKRASGPAKKHGNIPL
>NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein
MYAAIWRRLPGPRWLKALQALTLVAAVTAALFVWVFPAVTTGLGLFETTVAG
>NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase
MTRLTGAAAPPAPRAVTAPVSAHRGASVLGELLITAAAVLALFVVWQVWWTDVTGGRAQVAAVVAIETSFPTVPATPADSPASPLRTDAPPTLAEVPAGTGFAVVHVPRWGTDHALPVLEGVDARAVLDTGAAGHYPGTAPPGAVGNFALAAHRQTYGAAFRRVDELRVGDPIVVETAEAWLVYRVTADRVVAPEEVSVIAPVPGAPGEAATARMITFTTCHPLWSTAQRWVTHGELAGWLPRAAGVPAELGEVA

Crispr_ID: NZ_CP040915_3

• CRISPR_ID: NZ_CP040915_3
• CRISPR_location: 1057374-1057624
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_CP040915_3

Consensus_repeat	Method
CGACATCAACGACTCGTTCAACGAC	CRISPRCasFinder

spacers of NZ_CP040915_3

>3.1|1057399|47|NZ_CP040915|CRISPRCasFinder
TCGTTCAACGACGACCACTCCACGGACAACTCCGACCACTCGACGAA
>3.2|1057471|29|NZ_CP040915|CRISPRCasFinder
AACTCGGACAACTCCACCAACCTCGACGT
>3.3|1057525|20|NZ_CP040915|CRISPRCasFinder
GAGTCGGTCGACGTGGACGT
>3.4|1057570|29|NZ_CP040915|CRISPRCasFinder
GACAACGACGGCGTGGACATCGAGGAGGT

CRISPR arrays and Neighbor proteins around NZ_CP040915_3

CRISPR arrays

The CRISPR arrays of NZ_CP040915_3

>merge|NZ_CP040915|3|1057374-1057624|CRISPRCasFinder
CAACACCGACGTCGACATCAACGACTCGTTCAACGACGACCACTCCACGGACAACTCCGACCACTCGACGAACGTCATCAACGACTCGTTCAACGACAACTCGGACAACTCCACCAACCTCGACGTCGACATCGACGACTCCTTCAACGACGAGTCGGTCGACGTGGACGTGGACGTGGACGACTCCTTCAACCAGGACAACGACGGCGTGGACATCGAGGAGGTCGACGTCGACGACTCCTTCAACCAGG

>NZ_CP040915|3|3|1057374-1057624|CRISPRCasFinder
CAACACCGACGTCGACATCAACGAC	TCGTTCAACGACGACCACTCCACGGACAACTCCGACCACTCGACGAA
CGTCATCAACGACTCGTTCAACGAC	AACTCGGACAACTCCACCAACCTCGACGT
CGACATCGACGACTCCTTCAACGAC	GAGTCGGTCGACGTGGACGT
GGACGTGGACGACTCCTTCAACCAG	GACAACGACGGCGTGGACATCGAGGAGGT
CGACGTCGACGACTCCTTCAACCAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	unknown	unknown	gnl|CDD|178901
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	unknown	unknown	gnl|CDD|377577
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	unknown	unknown	gnl|CDD|320679
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	unknown	unknown	gnl|CDD|227136
NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173840
NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein	unknown	unknown	gnl|CDD|237171
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	unknown	unknown	gnl|CDD|381681
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	unknown	unknown	gnl|CDD|274635
NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	unknown	unknown	gnl|CDD|212667
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	unknown	unknown	gnl|CDD|379386
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239217
NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	unknown	unknown	gnl|CDD|227111

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	gnl|CDD|178901	PRK00148, PRK00148, Maf-like protein; Reviewed.	7.51248e-84
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	0
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	gnl|CDD|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	3.89009e-59
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	gnl|CDD|227136	COG4799, COG4799, Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) [Lipid metabolism].	0
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	gnl|CDD|379386	pfam13822, ACC_epsilon, Acyl-CoA carboxylase epsilon subunit. This family includes the epsilon subunits of propionyl-CoA carboxylase, EC:6.4.1.3, and acetyl-CoA carboxylase, EC:6.4.1.2. These enzymes are involved in the biosynthesis of long-chain fatty acids. The epsilon subunit is necessary for an efficient interaction between the alpha and beta subunits of these enzymes.	5.74672e-06
NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase	gnl|CDD|173840	cd01151, GCD, Glutaryl-CoA dehydrogenase. Glutaryl-CoA dehydrogenase (GCD). GCD is an acyl-CoA dehydrogenase, which catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and carbon dioxide in the catabolism of lysine, hydroxylysine, and tryptophan. It uses electron transfer flavoprotein (ETF) as an electron acceptor. GCD is a homotetramer. GCD deficiency leads to a severe neurological disorder in humans.	2.76489e-109
NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein	gnl|CDD|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	5.73429e-08
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	1.57556e-15
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.26291e-19
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.0804e-15
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.46344e-23
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	gnl|CDD|274635	TIGR03535, DapD_actino, 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. This enzyme is part of the diaminopimelate pathway of lysine biosynthesis. This model represents a clade of the enzyme specific to Actinobacteria. Alternate name: tetrahydrodipicolinate N-succinyltransferase.	1.01875e-171
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	gnl|CDD|381681	cd10031, UDG-F5_TTUDGB_like, Uracil DNA glycosylase family 5, includes Thermotoga maritima TTUDGB and similar proteins. Uracil DNA glycosylase family 5 includes Thermus thermophilus HB8 TTUDGB (also called UDGb) which is not only a UDG acting on double-stranded uracil-containing DNA, but also a hypoxanthine DNA glycosylase acting on double-stranded hypoxanthine-containing DNA (except for the C/I base pair), as well as a xanthine DNA glycosylase acting on both, double-stranded and single-stranded xanthine-containing DNA. TTUDGB also excises thymine from G:T mismatched DNA, and removes analogs of uracil from DNA, including 5-hydroxymethyluracil (hmU) and 5-fluorouracil (fU). This subfamily also contains Bradyrhizobium diazoefficiens family 5 homolog Blr5068 (UdgB) which has been found to efficiently excise uracil from ssDNA and dsDNA. Uracil-DNA glycosylases (UDGs) initiate repair of uracils in DNA. Similar to family 4 UDGs, members of this family possess four conserved cysteine residues required to coordinate the [4Fe-4S] iron-sulfur cluster. Uracil in DNA can arise as a result of mis-incorporation of dUMP residues by DNA polymerase or via deamination of cytosine. Uracil in DNA mispaired with guanine is one of the major pro-mutagenic events, causing G:C->A:T mutations. Thus, UDG is an essential enzyme for maintaining the integrity of genetic information. UDGs have been classified into various families on the basis of their substrate specificity, conserved motifs, and structural similarities. Although these families demonstrate different substrate specificities, often the function of one enzyme can be complemented by the other.	1.31618e-105
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	gnl|CDD|212667	cd10170, HSP70_NBD, Nucleotide-binding domain of the HSP70 family. HSP70 (70-kDa heat shock protein) family chaperones assist in protein folding and assembly and can direct incompetent "client" proteins towards degradation. Typically, HSP70s have a nucleotide-binding domain (NBD) and a substrate-binding domain (SBD). The nucleotide sits in a deep cleft formed between the two lobes of the NBD. The two subdomains of each lobe change conformation between ATP-bound, ADP-bound, and nucleotide-free states. ATP binding opens up the substrate-binding site; substrate-binding increases the rate of ATP hydrolysis. HSP70 chaperone activity is regulated by various co-chaperones: J-domain proteins and nucleotide exchange factors (NEFs). Some HSP70 family members are not chaperones but instead, function as NEFs to remove ADP from their HSP70 chaperone partners during the ATP hydrolysis cycle, some may function as both chaperones and NEFs.	1.18947e-94
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	gnl|CDD|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	3.09539e-11
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	gnl|CDD|227111	COG4770, COG4770, Acetyl/propionyl-CoA carboxylase, alpha subunit [Lipid metabolism].	0

Protein sequences

>NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator
MVAATPTHQVRSRQRALLEAIDVSGRPLNGVASRLARSGIEDPRVAEALVAQGDTLLPRDPAKAFEVYSQAVAAGADHTALAARRAQAAALSGNLDPAGRLVDELLSLPEPPDLGRAVDVAAEVWSRRGMLSRSADVYRWLGPDRIGASAPLAAIALVGCGDRAGMDDMLAAAGPPTSPTLLAAVPTLVCEGLRETLDSASTNAMGSLVRASDMMTASGSTLPMPMNPAALAALVALHLGELAVAESVTEDALAGNQGGAGCRPRLLLMRAWTAMLRDRPDHARAAITEARSAGEVLSPRDELFLRALEVGLARRTDDPPGLVQAWGRARESILHFPVDLFTLLPLGELLVAAARLRDSARIEGHVAEAWALLGRLGDPPLWTVPLHWAEVHAAILAERPGQLGPHAAALVRASGQSHFAAVLAAAGRVWVSVLAGDVDVEAVEIAARGLASVGLTWDGSRLAGHAAARAPERKDMARLLARARDLHPAAALAPEQAPTAPPGSNRSGTLLDDSGLSPREREIAAQVLAGRTYREIGDAIYISPRTVEHHVARIRRRLGASSRSELLARMRIALGEESWTS
>NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein
MTYSVGVDIGTSFVAAAITRIVDGRPQAPQPLHLGARSTATPSVMYFGDDGQVLVGDAAERRGTTDPDRVVRESKRRIGDSVPVVVGDLLVAPEDIYATMVRWVVDRADEQEGAPPDRVAVAHPVGWGAYKTGLVREALAGVGLGEVELISEPEAAALHYASFERVEVGSTIAVYDLGGGTFDVAILRKAETDTFDVLGRPEGIERLGGADFDEAVFRHVTAGLGEGFTSLDRTDPGVLVALSRMRRECTEAKEALSSDSETVVPVLLPGMQTQVRLVRSEFEELIAASVRETVASVEQALRTAQVEPEDLTAVLLIGGSSRVPLVAQLLSAELGRPIAVDADPKASICLGASLAAAYPGAIEGTAVLLGDDDVTVAPARAQAGDGVAPVTEPPSPAGAALAPAATAFVANAPHQHIGSRRGIKIAAIAGLVASITVFTTVAGQTPEVQELIKSSLRVSEAQAGTPAADGGEAVAAGEDGRGGAGGSGEGASSDRSGVARLNTVAPKPGDPTGKPKPTPTDEASTKVSATGSPTTGVPGTTSTGGKTTPGTNTPGGTATGDGSGTGGAPTGTPDGAGTPTTDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTEPPPEPEPTATATATATATEESTPPQDPPPPADTPPAEEPPATGAAITVPADPVLG
>NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf
MTTLLLASASPARLSTLRAAGLDPLVAASSVDEAKLLATATTEADRAGSAPVPPADQVLLLARAKAHDVREHPTLAREADVVLGCDSMLELEGEVLGKPTDAADAVVRWQRMRGRTGVLHTGHCLLDRDGREASATSSTVVHFADLTDAEVDAYVATGEPLWVAGAFTVDGLGGPFVAGIEGDYHGVVGVSLPLLRVLLAELGVAITDLWRPAAD
>NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase
MATVSTAPDLRPHPVTGRLFPSPVPPGTGWPEDPADAGTPVATTVPAVVDLARAAADVGELDARVSVCRACPRLVAWRESVATTGRRASFADQPYWGRPGPGVGDPAPQVLVVGLAPAANGTNRTGRMFTGDRSGDWIYAALYRAGYASQPDSWAAGDGLKLAGARIVAAVRCAPPANKPTPEERRTCGHWLDRDLELAAPGLRSMLALGAIGWDAALASARRLGWTVPRPKPRFGHGAQTELVAADGHPIRLLGSYHVSQQNTFTGRLTEAMLDAVIARL
>NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein
MTSTSSQLSPRGLTKVLIANRGEIAVRVARACADAGVATVAVYADSDRDALHVKLSDEAFALHGQRAAETYLDAGKILDVARRSGADAVHPGYGFLSENAGFAQAVLDAGLIWIGPPPAAIEALGDKVTARHIAQKVGAPLVPGTPDPVSGAEEVLAFADAHGLPIAIKAAFGGGGRGLKVARTREEIPELYESAVREAVAAFGRGECFVERFLDRPRHVETQCLADAAGNVVVVSTRDCSLQRRHQKLVEEAPAPFLTPAQEQTLVHASQAILREAGYVGAGTCEFLVGQDGTISFLEVNTRLQVEHPVTEEVTGIDLVREQLRLAAGEDLGYTEVATRGHAIELRINGEDPASGFMPAPGTISSLSWPSGPGVRVDSGVVAGDTISGAFDSMLAKIIITGATRTQAIERARRALRETEIVGLPTVVPFHRSVLTEPDFTADDGASSFGVHTTWIETDYAEHLRSLPSTRPAPAVAAPAEEPAEATERVIVEVGGKRLEVVIPAGLGISTGPRGAARRPVRRTVGRSSGTGGTNGAALTSPMQGTIVKVAVGDGEVVAQGDLVVVLEAMKMEQPLVAHRAGRVSGMAAAVGRNVATGAVICQIEPVEQAAPDAG
>NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein
MTASASRPPDARVHRQPGDGWVECSCGRRHWGLNGAAGLLLWRTGPAGPQLVLQHRALWSHHGGTWGLPGGALSDGETPVDGAVREAREEAGVVPAGLQVTAARALVHPDWAYTTVLAQATAPFEPAVTDPESLEVRWVDLASIEGFDLLPAFGDALPELRTMLRRLVLVVDAANVVGSRPDGWWADRAGATVRLRDHLAALARDGLDAVAVDLPGQRWYPEVVLVTEGAARGVDPTDGVRVVTAHGSGDDAVVQTVTAVLGATGDGVTDVAVATADRELSARVAALGARTLGPLLVRH
>NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase
MTERTAWAFGLATITDTGDTLEAWYPAPTLGAPPQDAAAPAELSAATSVDASRLVRTEVVRTEIDLDAAPASVADAYLRLHLLSHTLVQPNSINLDGIFGVLPTVVWTSAGPCAVEGFEATRARLRARGVLTVYGVDKFPRMVDYVVPAGVRIADGDRVRLGAHLAPGTTVMHEGFVNFNAGTLGRSMVEGRISQGVVVADGADVGGGASIMGTLSGGGKRVISVGPRSLLGANAGLGISLGADCVVEAGLYLTAGTKVSVIIGGGARPRHGQLDEPAVVSARDLSGRDNLLFRRNSLSGAVEAISRSGTGAELNAALHA
>NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein
MGCTGGAVLALGALGVAITGVVLALNTFVHSPASGTCTVALADGGVQRLDADQADNAALFAANAAHRDLPARAVTIAIATALQESKMRNIDYGDRDSVGLFQQRPSQGWGTVEQIMDPVYSTNAFYDVLVTVQGWESQEITDAAQRVQRSGFPLAYAQHEDRGRAFASALSGYSPASLSCHLDPVVEAPDGVGAPGSAGDGESTPTAVVEGTASAGPIAGATPPARLATIQQRLTRDFVDISATVVPAGVLQVDATSLPAGLDPAPARRGWAVAQWAVATASQTGARVVAVDGQVWVRDDGDDAAWLPLAEAGLPAALHDATASAAPGAVLIG
>NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein
MNTNEGPELILVRDLTALGRDPRSTQRASRSRALTRVRRGAYADARAWATATNSERHRLFVLSTMAGMRTPPVLSHESAAVLLGIPLMGPPPEKVHVAGDSASGGRSSACIQRHVVRPMPAITLVDGVAVTSAARTVVDLARSRPFTAGLVAADYVLRVGLVARAHLDEALDEVAGQRGARRARAVIDRADARAESVGESLSRAQMHLLGVPIPELQHVFYDADGFIGRTDFWWVEERKVGEFDGRIKYQPPERSGGLPPEKVVWREKRREDRLRRQIEGVVRWVWTEALNTSGFGRLLAGAGIYPVRPGVRP
>NZ_CP040915.1|WP_139927466.1|1042109_1043369_+|glutaryl-CoA-dehydrogenase
MTTTDGAAVTTGPRATAGAAVTTQSSAADLYARSDQYGYANLLTDDERAVLATLRTFLETQAAPLVADHWERGEFPTQLLGPLAGLDLMAPPSLTGGGARPRQLFEGFRVFELARTDASLATYFNGQASLFRSNVLLGGSAEQVARWDPLITRFEMTGVFALTEPEHGSDIAGGLATTARREGDTWVIDGAKRWIGSAAYSDYLTVVARDEADSKAKAFLVRTDAPGVELRKIGGKIALRMVNNADITLTGVRVSEEYRLQRVNSFADIAAMLRAMRAGVAWIATGVQAGAYEAALRYVLERHQFGRPIGGFQLVQDKLVRMLGNLTASLGMVVRLAQQQDASVYRDEDSALAKAWVSARMRETVALAREVAGGEGITLATDVARFFADAEAVYTYEGTNEINTLVVGRAITGLSAFTR
>NZ_CP040915.1|WP_139927475.1|1058149_1059367_+|hypothetical-protein
MTNIATSLLDFILGLLRDPEAAEKFKDDPEGELHKAGLDDVSSDDVDAVLPVVLDYAPVRVDSSFDRNYDTGGNSSWAGQSGGRDGRDGRDGRDDDHGSGGGRDHGGRDDDHGHGGRGDDDRDDDHGRDHDRGGRGDDDHSHAVQQITHVVNNYSYTSTVDDRDTITDQSVNQNIWAKGDVNQWFDNDAIVASGAGAIAAGDDVSVDDSTDNSTNVLAHDSNVEIGNTDVDINDSFNDDHSTDNSDHSTNVINDSFNDNSDNSTNLDVDIDDSFNDESVDVDVDVDDSFNEDNDGVDIEEVDVDDSFNQDNDGIDVEEVDVDVDNSNQGNTTISDNEVGNTEVSDNVVIADNEVGNTEISDNVVIEDSFDDNFSDNFTDDDFVDYDDQDVVDVDSSLNDNDIDAP
>NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA
MADLVKLVEQTIALVRDGDRADLSRRLEHTRQRLLDPSIRVIVVGEFKQGKSMLINALVGAPVCPVDDDIATAVPTVVRHGAAPSAVVLVPDPGGTDAEPTVQRRPVPLEELPAYVGEAGNPGNVKGLLGAEVTLPRAILAGGLAIIDSPGVGGLDSAHALTTLTALPTADAMLLVSDASQEYTEPEVAFLRQSMRVCPNVAGVLSKTDLYPQWRQVAQIDRGHLAKVDEEIPLFPVSSVLRLQAGRAKSQELNEESGFPGLIGYLRREIVGQAERLQRRSVAQDLRSTAEHLRLSLSSELAALENPEGTPQLLAELEVAKEHADEQRKKSARWQVTLNDGVADLISDMEFDLRDRLRAVQRDAEAAIDAGDPGPVWDQFTDWLEQRVAATVSETFLWTSERSQWLAEQVGALFAQDELRLPVLRVDDTDDVLDPVPLVPDLDAGHLSVTQKVLIGMRGSYGGVLMFGLLTGIAGMALINPISVAAGVLLGGKVYREDKEARLRRRQGEAKSIVRRQIDDVSFQVGKQLRDRLRIVQRTIRDHFTEIAEEHHRSLSDSVVAAQRAASIFSAERDQRIAVLKIDLNRVDALARKADALETADAEAPEPRSARAGRAGTPSRVGRPRGGAVVAEA
>NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein
MSTEGGVRLLLREALEVYADDPVAATSLHGWASRLDGPLRVAIAGMVKAGKSTLLNAILGEELAPTDTGECTRVVTWYRHGATPRVTLYPRDGEPRQLPLRRVEGRLRLDLGGTPAEEVARLVVDWPTAGLRDLTLIDTPGIASLSTDVSARATAFLTPEDSPSEADAVVYLMRHMHGSDIHFLESFRDAEAGRSGTVNALAVLSRADEVGAGRLDSMISARDVARRYREDPSLRPLALSVVPIAGLLAQSARTLRQSEFAALRELAELGREERERLLLSADRFTRAEITPAVDVTMRAALVERLGLFGLRLALVLIRSGLDDPTDLARELARRSGLGELQRLIDGQFQARSAQLKARTALVGLETLLRTRPRPGTERLATELERIQAGAHEFRELRLLGTARTVGLGLPRDLEAEAERLVGGRGVAPARRLNLADGASDAKIRAAALESLRRWRALAENPLTDRSTAGACEVVARSCEALVVAAQPVAGPTTRPQLRPEPARGGG
>NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein
MTYQADAPVHREVEAPGALRTSRTLWLLSFVAGLVAVGFSWLNRDDGKQRLLETVTDLAPGRDAATLEALANLVFWGSLGAIALVVVLEALLLRTMMRRRAWPRVAAFFVLVVHAAVMVLAEAYLAAPGGAGAAVRWPLLIQLGLAVVAWIVSLSPAASRWFRA
>NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein
MRRIALDPLEATSLGLPGHDHEMPDLSPAGLAARTDLDRATLAELEAVAPVDGVDRVTHAAMRERLGVAVELADAGELTRELNVIASPVQAVREVFDLMPTATAADWETIAERLRAVPAALDGYQDSLLAARGAGHVAALRQVEACLKQADELADADTSFFTTFTAGAQPDGEAPHRALAAELEAGARDARQAYADLARMLGEELAPDAPELDAVGRERYGLWSRYFLGAVVDLDETYAWGQEDLARVVAEQQAVAEELYGPGTGIREAMDRLDKDPDRMLHGTPALREWMQATSDEAVAALTDAQFDIPEPVRRLECMIAPTQSGGIYYTGPSADFSRPGRMWWSVPAGVTDFATWREKTTVYHEGVPGHHLQIGQTVYRSGLLNMWRRMASWVSGHGEGWALYAERLMADLGFLDDPGDRMGMLDGQRLRAARVVLDIGVHLGKPAPDEWGGGTWDAAKAWPFLKANANMAEGFLAFELDRYLGWPGQAPAYKIGQRLWEEIRDDAGTAARRDGGELDLKAFHRRALDIGSVGLDVLREALV
>NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein
MGRWSRPLAAAFVEWLGAPDGLEWLDVGCGTGAVTAAIVTGAAPSAVLAIDPSPGFVATARRLTASPLARFTVGDAATLPMGDDAVDRCVSGLVVNFLPDASAAVAEMRRVTRRGGWVAAYVWDYAGGMELLREFWAAAVTVDPGAAQMDERHRFPLCAPGPLGELWRSAGLDGVESRPLTVSTHFPDFDDLWAPFLGGQGPAPAYVGSLTPERRPALARELRRRLHPSADGAIELTARAWAVRGRRR
>NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon
MTSPAVRVLRGRPDEVELAALVAGIVAARGRADELGGLPDEAAECVRSRWSERARVLGMATAPDAGAWRWSLHP
>NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta
MTDSSIDLSAPVAGASPAGDSPATPPTAVPAQPPTTAAKVADLAAREQNLTDAAATAVEKQHKRGKKSARERIEALLDPGSFTELDAFATHRSSNFGLDKKRIPGDGVVTGYGTVDGRQVCIYSQDFTVFGGSLGEVHGQKITKVMDMALTTGVPLIGISDGGGARIQEGVAALTQFAEIFRRNVAASGVIPQISLILGPSAGGAVYSPALTDFIVMAEGTSNMFITGPDVIKAVTGEEVGFEELGGAATHNQRSGVAHYQAADEDDAVDYVRALLSYLPSNNLSEPPSWPVSADEAEAALEVTDTDRELDTLVPDSDNQPYDMRVVVEHVLDDHEMLEVQPGYAPNMITAFGHVEGRPVGVVANQPQQMAGTLDINAAEKAARFVRTCDAFNIPVLTFVDVPGFLPGTDQEWNGIIRRGAKLIYAYAEATVPLVTLITRKAYGGAYIVMGSKKLGADVNLAWPTAQIAVMGSGGAVNILQRGALKKVAEEGGDVEAERARLVAEYEETLVNPWEAAERGFVDAVITPADTRVQVVKALRALRTKRASGPAKKHGNIPL
>NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein
MYAAIWRRLPGPRWLKALQALTLVAAVTAALFVWVFPAVTTGLGLFETTVAG
>NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase
MTRLTGAAAPPAPRAVTAPVSAHRGASVLGELLITAAAVLALFVVWQVWWTDVTGGRAQVAAVVAIETSFPTVPATPADSPASPLRTDAPPTLAEVPAGTGFAVVHVPRWGTDHALPVLEGVDARAVLDTGAAGHYPGTAPPGAVGNFALAAHRQTYGAAFRRVDELRVGDPIVVETAEAWLVYRVTADRVVAPEEVSVIAPVPGAPGEAATARMITFTTCHPLWSTAQRWVTHGELAGWLPRAAGVPAELGEVA

Crispr_ID: NZ_CP040915_6

• CRISPR_ID: NZ_CP040915_6
• CRISPR_location: 1059166-1059262
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_6

Consensus_repeat	Method
CGACATCAACGACTCGTTCAACGAC	CRISPRCasFinder

spacers of NZ_CP040915_6

>6.1|1059191|47|NZ_CP040915|CRISPRCasFinder
GTTATCGCGGACAACGAGGTGGGCAACACCGAGATCTCCGACAACGT

CRISPR arrays and Neighbor proteins around NZ_CP040915_6

CRISPR arrays

The CRISPR arrays of NZ_CP040915_6

>merge|NZ_CP040915|6|1059166-1059262|CRISPRCasFinder
CAACACCGAGGTCTCGGACAACGTCGTTATCGCGGACAACGAGGTGGGCAACACCGAGATCTCCGACAACGTCGTCATCGAGGACTCCTTCGACGAC

>NZ_CP040915|6|6|1059166-1059262|CRISPRCasFinder
CAACACCGAGGTCTCGGACAACGTC	GTTATCGCGGACAACGAGGTGGGCAACACCGAGATCTCCGACAACGT
CGTCATCGAGGACTCCTTCGACGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	unknown	unknown	gnl|CDD|178901
NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein	unknown	unknown	gnl|CDD|237171
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	unknown	unknown	gnl|CDD|377577
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	unknown	unknown	gnl|CDD|320679
NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase	unknown	unknown	gnl|CDD|223417
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	unknown	unknown	gnl|CDD|227136
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	unknown	unknown	gnl|CDD|212667
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	unknown	unknown	gnl|CDD|381681
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	unknown	unknown	gnl|CDD|274635
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	unknown	unknown	gnl|CDD|379386
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239217
NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	unknown	unknown	gnl|CDD|227111

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	gnl|CDD|178901	PRK00148, PRK00148, Maf-like protein; Reviewed.	7.51248e-84
NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein	gnl|CDD|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	5.05543e-05
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	0
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	gnl|CDD|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	3.89009e-59
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	gnl|CDD|379386	pfam13822, ACC_epsilon, Acyl-CoA carboxylase epsilon subunit. This family includes the epsilon subunits of propionyl-CoA carboxylase, EC:6.4.1.3, and acetyl-CoA carboxylase, EC:6.4.1.2. These enzymes are involved in the biosynthesis of long-chain fatty acids. The epsilon subunit is necessary for an efficient interaction between the alpha and beta subunits of these enzymes.	5.74672e-06
NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase	gnl|CDD|223417	COG0340, BirA, Biotin-(acetyl-CoA carboxylase) ligase [Coenzyme metabolism].	2.53196e-55
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	gnl|CDD|227136	COG4799, COG4799, Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) [Lipid metabolism].	0
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	gnl|CDD|212667	cd10170, HSP70_NBD, Nucleotide-binding domain of the HSP70 family. HSP70 (70-kDa heat shock protein) family chaperones assist in protein folding and assembly and can direct incompetent "client" proteins towards degradation. Typically, HSP70s have a nucleotide-binding domain (NBD) and a substrate-binding domain (SBD). The nucleotide sits in a deep cleft formed between the two lobes of the NBD. The two subdomains of each lobe change conformation between ATP-bound, ADP-bound, and nucleotide-free states. ATP binding opens up the substrate-binding site; substrate-binding increases the rate of ATP hydrolysis. HSP70 chaperone activity is regulated by various co-chaperones: J-domain proteins and nucleotide exchange factors (NEFs). Some HSP70 family members are not chaperones but instead, function as NEFs to remove ADP from their HSP70 chaperone partners during the ATP hydrolysis cycle, some may function as both chaperones and NEFs.	1.18947e-94
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.26291e-19
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.0804e-15
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.46344e-23
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	gnl|CDD|274635	TIGR03535, DapD_actino, 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. This enzyme is part of the diaminopimelate pathway of lysine biosynthesis. This model represents a clade of the enzyme specific to Actinobacteria. Alternate name: tetrahydrodipicolinate N-succinyltransferase.	1.01875e-171
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	gnl|CDD|381681	cd10031, UDG-F5_TTUDGB_like, Uracil DNA glycosylase family 5, includes Thermotoga maritima TTUDGB and similar proteins. Uracil DNA glycosylase family 5 includes Thermus thermophilus HB8 TTUDGB (also called UDGb) which is not only a UDG acting on double-stranded uracil-containing DNA, but also a hypoxanthine DNA glycosylase acting on double-stranded hypoxanthine-containing DNA (except for the C/I base pair), as well as a xanthine DNA glycosylase acting on both, double-stranded and single-stranded xanthine-containing DNA. TTUDGB also excises thymine from G:T mismatched DNA, and removes analogs of uracil from DNA, including 5-hydroxymethyluracil (hmU) and 5-fluorouracil (fU). This subfamily also contains Bradyrhizobium diazoefficiens family 5 homolog Blr5068 (UdgB) which has been found to efficiently excise uracil from ssDNA and dsDNA. Uracil-DNA glycosylases (UDGs) initiate repair of uracils in DNA. Similar to family 4 UDGs, members of this family possess four conserved cysteine residues required to coordinate the [4Fe-4S] iron-sulfur cluster. Uracil in DNA can arise as a result of mis-incorporation of dUMP residues by DNA polymerase or via deamination of cytosine. Uracil in DNA mispaired with guanine is one of the major pro-mutagenic events, causing G:C->A:T mutations. Thus, UDG is an essential enzyme for maintaining the integrity of genetic information. UDGs have been classified into various families on the basis of their substrate specificity, conserved motifs, and structural similarities. Although these families demonstrate different substrate specificities, often the function of one enzyme can be complemented by the other.	1.31618e-105
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	1.57556e-15
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	gnl|CDD|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	3.09539e-11
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	gnl|CDD|227111	COG4770, COG4770, Acetyl/propionyl-CoA carboxylase, alpha subunit [Lipid metabolism].	0

Protein sequences

>NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein
MATTIASQLLEFLMNLMRDPQAAAEFRADPEAALDSAGLADVCSADVDAVMPVVMDHAVKVGSSFGREARDGRDGRDGRDGRDGRDGRDGRDGHGHKDDDKHDRDDDHGHGRDHGHGRDDDDHSHAVQQISHVVNNYSYTSTVDDRDTITDQSVNQNIWAKGDVNQWFDNDAMIASGDDSIAAGGDVDVDNSTNNSINVLAHDSNVEIGNTDVDINDSFNDDHSTDNSDHSTNVINDSFNDNSDNSTNLDVDIDDSFNDESVDVDVDVDDSFNQDNDGVDIEEVDVDDSFNQDNDGIDVEEVDVDVDNSNQDNVTISDNEVGNTEISDNVVIADNEVGNTEITDNVVIEDSFDDNFSNNFTDDDVLDIDDQDFVDVDNTANDNELEL
>NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator
MVAATPTHQVRSRQRALLEAIDVSGRPLNGVASRLARSGIEDPRVAEALVAQGDTLLPRDPAKAFEVYSQAVAAGADHTALAARRAQAAALSGNLDPAGRLVDELLSLPEPPDLGRAVDVAAEVWSRRGMLSRSADVYRWLGPDRIGASAPLAAIALVGCGDRAGMDDMLAAAGPPTSPTLLAAVPTLVCEGLRETLDSASTNAMGSLVRASDMMTASGSTLPMPMNPAALAALVALHLGELAVAESVTEDALAGNQGGAGCRPRLLLMRAWTAMLRDRPDHARAAITEARSAGEVLSPRDELFLRALEVGLARRTDDPPGLVQAWGRARESILHFPVDLFTLLPLGELLVAAARLRDSARIEGHVAEAWALLGRLGDPPLWTVPLHWAEVHAAILAERPGQLGPHAAALVRASGQSHFAAVLAAAGRVWVSVLAGDVDVEAVEIAARGLASVGLTWDGSRLAGHAAARAPERKDMARLLARARDLHPAAALAPEQAPTAPPGSNRSGTLLDDSGLSPREREIAAQVLAGRTYREIGDAIYISPRTVEHHVARIRRRLGASSRSELLARMRIALGEESWTS
>NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein
MTYSVGVDIGTSFVAAAITRIVDGRPQAPQPLHLGARSTATPSVMYFGDDGQVLVGDAAERRGTTDPDRVVRESKRRIGDSVPVVVGDLLVAPEDIYATMVRWVVDRADEQEGAPPDRVAVAHPVGWGAYKTGLVREALAGVGLGEVELISEPEAAALHYASFERVEVGSTIAVYDLGGGTFDVAILRKAETDTFDVLGRPEGIERLGGADFDEAVFRHVTAGLGEGFTSLDRTDPGVLVALSRMRRECTEAKEALSSDSETVVPVLLPGMQTQVRLVRSEFEELIAASVRETVASVEQALRTAQVEPEDLTAVLLIGGSSRVPLVAQLLSAELGRPIAVDADPKASICLGASLAAAYPGAIEGTAVLLGDDDVTVAPARAQAGDGVAPVTEPPSPAGAALAPAATAFVANAPHQHIGSRRGIKIAAIAGLVASITVFTTVAGQTPEVQELIKSSLRVSEAQAGTPAADGGEAVAAGEDGRGGAGGSGEGASSDRSGVARLNTVAPKPGDPTGKPKPTPTDEASTKVSATGSPTTGVPGTTSTGGKTTPGTNTPGGTATGDGSGTGGAPTGTPDGAGTPTTDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTEPPPEPEPTATATATATATEESTPPQDPPPPADTPPAEEPPATGAAITVPADPVLG
>NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf
MTTLLLASASPARLSTLRAAGLDPLVAASSVDEAKLLATATTEADRAGSAPVPPADQVLLLARAKAHDVREHPTLAREADVVLGCDSMLELEGEVLGKPTDAADAVVRWQRMRGRTGVLHTGHCLLDRDGREASATSSTVVHFADLTDAEVDAYVATGEPLWVAGAFTVDGLGGPFVAGIEGDYHGVVGVSLPLLRVLLAELGVAITDLWRPAAD
>NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase
MATVSTAPDLRPHPVTGRLFPSPVPPGTGWPEDPADAGTPVATTVPAVVDLARAAADVGELDARVSVCRACPRLVAWRESVATTGRRASFADQPYWGRPGPGVGDPAPQVLVVGLAPAANGTNRTGRMFTGDRSGDWIYAALYRAGYASQPDSWAAGDGLKLAGARIVAAVRCAPPANKPTPEERRTCGHWLDRDLELAAPGLRSMLALGAIGWDAALASARRLGWTVPRPKPRFGHGAQTELVAADGHPIRLLGSYHVSQQNTFTGRLTEAMLDAVIARL
>NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein
MTSTSSQLSPRGLTKVLIANRGEIAVRVARACADAGVATVAVYADSDRDALHVKLSDEAFALHGQRAAETYLDAGKILDVARRSGADAVHPGYGFLSENAGFAQAVLDAGLIWIGPPPAAIEALGDKVTARHIAQKVGAPLVPGTPDPVSGAEEVLAFADAHGLPIAIKAAFGGGGRGLKVARTREEIPELYESAVREAVAAFGRGECFVERFLDRPRHVETQCLADAAGNVVVVSTRDCSLQRRHQKLVEEAPAPFLTPAQEQTLVHASQAILREAGYVGAGTCEFLVGQDGTISFLEVNTRLQVEHPVTEEVTGIDLVREQLRLAAGEDLGYTEVATRGHAIELRINGEDPASGFMPAPGTISSLSWPSGPGVRVDSGVVAGDTISGAFDSMLAKIIITGATRTQAIERARRALRETEIVGLPTVVPFHRSVLTEPDFTADDGASSFGVHTTWIETDYAEHLRSLPSTRPAPAVAAPAEEPAEATERVIVEVGGKRLEVVIPAGLGISTGPRGAARRPVRRTVGRSSGTGGTNGAALTSPMQGTIVKVAVGDGEVVAQGDLVVVLEAMKMEQPLVAHRAGRVSGMAAAVGRNVATGAVICQIEPVEQAAPDAG
>NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein
MTASASRPPDARVHRQPGDGWVECSCGRRHWGLNGAAGLLLWRTGPAGPQLVLQHRALWSHHGGTWGLPGGALSDGETPVDGAVREAREEAGVVPAGLQVTAARALVHPDWAYTTVLAQATAPFEPAVTDPESLEVRWVDLASIEGFDLLPAFGDALPELRTMLRRLVLVVDAANVVGSRPDGWWADRAGATVRLRDHLAALARDGLDAVAVDLPGQRWYPEVVLVTEGAARGVDPTDGVRVVTAHGSGDDAVVQTVTAVLGATGDGVTDVAVATADRELSARVAALGARTLGPLLVRH
>NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase
MTERTAWAFGLATITDTGDTLEAWYPAPTLGAPPQDAAAPAELSAATSVDASRLVRTEVVRTEIDLDAAPASVADAYLRLHLLSHTLVQPNSINLDGIFGVLPTVVWTSAGPCAVEGFEATRARLRARGVLTVYGVDKFPRMVDYVVPAGVRIADGDRVRLGAHLAPGTTVMHEGFVNFNAGTLGRSMVEGRISQGVVVADGADVGGGASIMGTLSGGGKRVISVGPRSLLGANAGLGISLGADCVVEAGLYLTAGTKVSVIIGGGARPRHGQLDEPAVVSARDLSGRDNLLFRRNSLSGAVEAISRSGTGAELNAALHA
>NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein
MGCTGGAVLALGALGVAITGVVLALNTFVHSPASGTCTVALADGGVQRLDADQADNAALFAANAAHRDLPARAVTIAIATALQESKMRNIDYGDRDSVGLFQQRPSQGWGTVEQIMDPVYSTNAFYDVLVTVQGWESQEITDAAQRVQRSGFPLAYAQHEDRGRAFASALSGYSPASLSCHLDPVVEAPDGVGAPGSAGDGESTPTAVVEGTASAGPIAGATPPARLATIQQRLTRDFVDISATVVPAGVLQVDATSLPAGLDPAPARRGWAVAQWAVATASQTGARVVAVDGQVWVRDDGDDAAWLPLAEAGLPAALHDATASAAPGAVLIG
>NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein
MNTNEGPELILVRDLTALGRDPRSTQRASRSRALTRVRRGAYADARAWATATNSERHRLFVLSTMAGMRTPPVLSHESAAVLLGIPLMGPPPEKVHVAGDSASGGRSSACIQRHVVRPMPAITLVDGVAVTSAARTVVDLARSRPFTAGLVAADYVLRVGLVARAHLDEALDEVAGQRGARRARAVIDRADARAESVGESLSRAQMHLLGVPIPELQHVFYDADGFIGRTDFWWVEERKVGEFDGRIKYQPPERSGGLPPEKVVWREKRREDRLRRQIEGVVRWVWTEALNTSGFGRLLAGAGIYPVRPGVRP
>NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA
MADLVKLVEQTIALVRDGDRADLSRRLEHTRQRLLDPSIRVIVVGEFKQGKSMLINALVGAPVCPVDDDIATAVPTVVRHGAAPSAVVLVPDPGGTDAEPTVQRRPVPLEELPAYVGEAGNPGNVKGLLGAEVTLPRAILAGGLAIIDSPGVGGLDSAHALTTLTALPTADAMLLVSDASQEYTEPEVAFLRQSMRVCPNVAGVLSKTDLYPQWRQVAQIDRGHLAKVDEEIPLFPVSSVLRLQAGRAKSQELNEESGFPGLIGYLRREIVGQAERLQRRSVAQDLRSTAEHLRLSLSSELAALENPEGTPQLLAELEVAKEHADEQRKKSARWQVTLNDGVADLISDMEFDLRDRLRAVQRDAEAAIDAGDPGPVWDQFTDWLEQRVAATVSETFLWTSERSQWLAEQVGALFAQDELRLPVLRVDDTDDVLDPVPLVPDLDAGHLSVTQKVLIGMRGSYGGVLMFGLLTGIAGMALINPISVAAGVLLGGKVYREDKEARLRRRQGEAKSIVRRQIDDVSFQVGKQLRDRLRIVQRTIRDHFTEIAEEHHRSLSDSVVAAQRAASIFSAERDQRIAVLKIDLNRVDALARKADALETADAEAPEPRSARAGRAGTPSRVGRPRGGAVVAEA
>NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein
MSTEGGVRLLLREALEVYADDPVAATSLHGWASRLDGPLRVAIAGMVKAGKSTLLNAILGEELAPTDTGECTRVVTWYRHGATPRVTLYPRDGEPRQLPLRRVEGRLRLDLGGTPAEEVARLVVDWPTAGLRDLTLIDTPGIASLSTDVSARATAFLTPEDSPSEADAVVYLMRHMHGSDIHFLESFRDAEAGRSGTVNALAVLSRADEVGAGRLDSMISARDVARRYREDPSLRPLALSVVPIAGLLAQSARTLRQSEFAALRELAELGREERERLLLSADRFTRAEITPAVDVTMRAALVERLGLFGLRLALVLIRSGLDDPTDLARELARRSGLGELQRLIDGQFQARSAQLKARTALVGLETLLRTRPRPGTERLATELERIQAGAHEFRELRLLGTARTVGLGLPRDLEAEAERLVGGRGVAPARRLNLADGASDAKIRAAALESLRRWRALAENPLTDRSTAGACEVVARSCEALVVAAQPVAGPTTRPQLRPEPARGGG
>NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein
MTYQADAPVHREVEAPGALRTSRTLWLLSFVAGLVAVGFSWLNRDDGKQRLLETVTDLAPGRDAATLEALANLVFWGSLGAIALVVVLEALLLRTMMRRRAWPRVAAFFVLVVHAAVMVLAEAYLAAPGGAGAAVRWPLLIQLGLAVVAWIVSLSPAASRWFRA
>NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein
MRRIALDPLEATSLGLPGHDHEMPDLSPAGLAARTDLDRATLAELEAVAPVDGVDRVTHAAMRERLGVAVELADAGELTRELNVIASPVQAVREVFDLMPTATAADWETIAERLRAVPAALDGYQDSLLAARGAGHVAALRQVEACLKQADELADADTSFFTTFTAGAQPDGEAPHRALAAELEAGARDARQAYADLARMLGEELAPDAPELDAVGRERYGLWSRYFLGAVVDLDETYAWGQEDLARVVAEQQAVAEELYGPGTGIREAMDRLDKDPDRMLHGTPALREWMQATSDEAVAALTDAQFDIPEPVRRLECMIAPTQSGGIYYTGPSADFSRPGRMWWSVPAGVTDFATWREKTTVYHEGVPGHHLQIGQTVYRSGLLNMWRRMASWVSGHGEGWALYAERLMADLGFLDDPGDRMGMLDGQRLRAARVVLDIGVHLGKPAPDEWGGGTWDAAKAWPFLKANANMAEGFLAFELDRYLGWPGQAPAYKIGQRLWEEIRDDAGTAARRDGGELDLKAFHRRALDIGSVGLDVLREALV
>NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein
MGRWSRPLAAAFVEWLGAPDGLEWLDVGCGTGAVTAAIVTGAAPSAVLAIDPSPGFVATARRLTASPLARFTVGDAATLPMGDDAVDRCVSGLVVNFLPDASAAVAEMRRVTRRGGWVAAYVWDYAGGMELLREFWAAAVTVDPGAAQMDERHRFPLCAPGPLGELWRSAGLDGVESRPLTVSTHFPDFDDLWAPFLGGQGPAPAYVGSLTPERRPALARELRRRLHPSADGAIELTARAWAVRGRRR
>NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon
MTSPAVRVLRGRPDEVELAALVAGIVAARGRADELGGLPDEAAECVRSRWSERARVLGMATAPDAGAWRWSLHP
>NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta
MTDSSIDLSAPVAGASPAGDSPATPPTAVPAQPPTTAAKVADLAAREQNLTDAAATAVEKQHKRGKKSARERIEALLDPGSFTELDAFATHRSSNFGLDKKRIPGDGVVTGYGTVDGRQVCIYSQDFTVFGGSLGEVHGQKITKVMDMALTTGVPLIGISDGGGARIQEGVAALTQFAEIFRRNVAASGVIPQISLILGPSAGGAVYSPALTDFIVMAEGTSNMFITGPDVIKAVTGEEVGFEELGGAATHNQRSGVAHYQAADEDDAVDYVRALLSYLPSNNLSEPPSWPVSADEAEAALEVTDTDRELDTLVPDSDNQPYDMRVVVEHVLDDHEMLEVQPGYAPNMITAFGHVEGRPVGVVANQPQQMAGTLDINAAEKAARFVRTCDAFNIPVLTFVDVPGFLPGTDQEWNGIIRRGAKLIYAYAEATVPLVTLITRKAYGGAYIVMGSKKLGADVNLAWPTAQIAVMGSGGAVNILQRGALKKVAEEGGDVEAERARLVAEYEETLVNPWEAAERGFVDAVITPADTRVQVVKALRALRTKRASGPAKKHGNIPL
>NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein
MYAAIWRRLPGPRWLKALQALTLVAAVTAALFVWVFPAVTTGLGLFETTVAG
>NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase
MTRLTGAAAPPAPRAVTAPVSAHRGASVLGELLITAAAVLALFVVWQVWWTDVTGGRAQVAAVVAIETSFPTVPATPADSPASPLRTDAPPTLAEVPAGTGFAVVHVPRWGTDHALPVLEGVDARAVLDTGAAGHYPGTAPPGAVGNFALAAHRQTYGAAFRRVDELRVGDPIVVETAEAWLVYRVTADRVVAPEEVSVIAPVPGAPGEAATARMITFTTCHPLWSTAQRWVTHGELAGWLPRAAGVPAELGEVA
>NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase
MPDDASPLPPFTRVVRVVQTGSTNTDLREAVTAEPGAWPHLSVLVAETQDAGRGRAGRSWDTAPGTALTASVLLRPRVPPGRLPWLTLLAGLAVQRATAELTGVRTGLKWPNDVLVLDVGEEVDGWGTDRKVAGILAEALPAADSHDAGPHAAGPHAAGPHAAGPHAGAGHAGSLAVVLGIGVNVAQTRDQLPVPWATSLRLAADARVTTPGAEELLSAVGRHLADLLRRWEAAAGDAGAAGLAEDVARVCVTLGRSVRAELPGGIEVTGTATALDNDGHLLLRTPEGTERTVRAGDVRHVRAG

Crispr_ID: NZ_CP040915_5

• CRISPR_ID: NZ_CP040915_5
• CRISPR_location: 1058686-1059077
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 6 spacers

Consensus repeat of NZ_CP040915_5

Consensus_repeat	Method
CGACATCAACGACTCGTTCAACGAC	CRISPRCasFinder

spacers of NZ_CP040915_5

>5.1|1058711|38|NZ_CP040915|CRISPRCasFinder
GACGCCATCGTCGCCTCGGGCGCCGGTGCGATCGCCGC
>5.2|1058774|53|NZ_CP040915|CRISPRCasFinder
TCCACGGACAACTCCACCAACGTGCTGGCGCACGACTCCAACGTGGAGATCGG
>5.3|1058852|47|NZ_CP040915|CRISPRCasFinder
TCGTTCAACGACGATCACTCCACGGACAACTCCGACCACTCGACGAA
>5.4|1058924|29|NZ_CP040915|CRISPRCasFinder
AACTCGGACAACTCCACCAACCTCGACGT
>5.5|1058978|20|NZ_CP040915|CRISPRCasFinder
GAGTCGGTCGACGTGGACGT
>5.6|1059023|29|NZ_CP040915|CRISPRCasFinder
GACAACGACGGCGTGGACATCGAGGAGGT

CRISPR arrays and Neighbor proteins around NZ_CP040915_5

CRISPR arrays

The CRISPR arrays of NZ_CP040915_5

>merge|NZ_CP040915|5|1058686-1059077|CRISPRCasFinder
CGACGTGAACCAGTGGTTCGACAACGACGCCATCGTCGCCTCGGGCGCCGGTGCGATCGCCGCCGGCGACGACGTCTCGGTGGACGACTCCACGGACAACTCCACCAACGTGCTGGCGCACGACTCCAACGTGGAGATCGGCAACACCGACGTCGACATCAACGACTCGTTCAACGACGATCACTCCACGGACAACTCCGACCACTCGACGAACGTCATCAACGACTCGTTCAACGACAACTCGGACAACTCCACCAACCTCGACGTCGACATCGACGACTCCTTCAACGACGAGTCGGTCGACGTGGACGTGGACGTGGACGACTCGTTCAACGAGGACAACGACGGCGTGGACATCGAGGAGGTCGACGTCGACGACTCCTTCAACCAGG

>NZ_CP040915|5|5|1058686-1059077|CRISPRCasFinder
CGACGTGAACCAGTGGTTCGACAAC	GACGCCATCGTCGCCTCGGGCGCCGGTGCGATCGCCGC
CGGCGACGACGTCTCGGTGGACGAC	TCCACGGACAACTCCACCAACGTGCTGGCGCACGACTCCAACGTGGAGATCGG
CAACACCGACGTCGACATCAACGAC	TCGTTCAACGACGATCACTCCACGGACAACTCCGACCACTCGACGAA
CGTCATCAACGACTCGTTCAACGAC	AACTCGGACAACTCCACCAACCTCGACGT
CGACATCGACGACTCCTTCAACGAC	GAGTCGGTCGACGTGGACGT
GGACGTGGACGACTCGTTCAACGAG	GACAACGACGGCGTGGACATCGAGGAGGT
CGACGTCGACGACTCCTTCAACCAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	unknown	unknown	gnl|CDD|178901
NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein	unknown	unknown	gnl|CDD|237171
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	unknown	unknown	gnl|CDD|377577
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	unknown	unknown	gnl|CDD|320679
NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase	unknown	unknown	gnl|CDD|223417
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	unknown	unknown	gnl|CDD|227136
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	unknown	unknown	gnl|CDD|212667
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	unknown	unknown	gnl|CDD|381681
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	unknown	unknown	gnl|CDD|274635
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	unknown	unknown	gnl|CDD|206739
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	unknown	unknown	gnl|CDD|379386
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239217
NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	unknown	unknown	gnl|CDD|227111

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf	gnl|CDD|178901	PRK00148, PRK00148, Maf-like protein; Reviewed.	7.51248e-84
NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein	gnl|CDD|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	5.05543e-05
NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	0
NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase	gnl|CDD|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	3.89009e-59
NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon	gnl|CDD|379386	pfam13822, ACC_epsilon, Acyl-CoA carboxylase epsilon subunit. This family includes the epsilon subunits of propionyl-CoA carboxylase, EC:6.4.1.3, and acetyl-CoA carboxylase, EC:6.4.1.2. These enzymes are involved in the biosynthesis of long-chain fatty acids. The epsilon subunit is necessary for an efficient interaction between the alpha and beta subunits of these enzymes.	5.74672e-06
NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase	gnl|CDD|223417	COG0340, BirA, Biotin-(acetyl-CoA carboxylase) ligase [Coenzyme metabolism].	2.53196e-55
NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta	gnl|CDD|227136	COG4799, COG4799, Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) [Lipid metabolism].	0
NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein	gnl|CDD|212667	cd10170, HSP70_NBD, Nucleotide-binding domain of the HSP70 family. HSP70 (70-kDa heat shock protein) family chaperones assist in protein folding and assembly and can direct incompetent "client" proteins towards degradation. Typically, HSP70s have a nucleotide-binding domain (NBD) and a substrate-binding domain (SBD). The nucleotide sits in a deep cleft formed between the two lobes of the NBD. The two subdomains of each lobe change conformation between ATP-bound, ADP-bound, and nucleotide-free states. ATP binding opens up the substrate-binding site; substrate-binding increases the rate of ATP hydrolysis. HSP70 chaperone activity is regulated by various co-chaperones: J-domain proteins and nucleotide exchange factors (NEFs). Some HSP70 family members are not chaperones but instead, function as NEFs to remove ADP from their HSP70 chaperone partners during the ATP hydrolysis cycle, some may function as both chaperones and NEFs.	1.18947e-94
NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.26291e-19
NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.0804e-15
NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	5.46344e-23
NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase	gnl|CDD|274635	TIGR03535, DapD_actino, 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. This enzyme is part of the diaminopimelate pathway of lysine biosynthesis. This model represents a clade of the enzyme specific to Actinobacteria. Alternate name: tetrahydrodipicolinate N-succinyltransferase.	1.01875e-171
NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase	gnl|CDD|381681	cd10031, UDG-F5_TTUDGB_like, Uracil DNA glycosylase family 5, includes Thermotoga maritima TTUDGB and similar proteins. Uracil DNA glycosylase family 5 includes Thermus thermophilus HB8 TTUDGB (also called UDGb) which is not only a UDG acting on double-stranded uracil-containing DNA, but also a hypoxanthine DNA glycosylase acting on double-stranded hypoxanthine-containing DNA (except for the C/I base pair), as well as a xanthine DNA glycosylase acting on both, double-stranded and single-stranded xanthine-containing DNA. TTUDGB also excises thymine from G:T mismatched DNA, and removes analogs of uracil from DNA, including 5-hydroxymethyluracil (hmU) and 5-fluorouracil (fU). This subfamily also contains Bradyrhizobium diazoefficiens family 5 homolog Blr5068 (UdgB) which has been found to efficiently excise uracil from ssDNA and dsDNA. Uracil-DNA glycosylases (UDGs) initiate repair of uracils in DNA. Similar to family 4 UDGs, members of this family possess four conserved cysteine residues required to coordinate the [4Fe-4S] iron-sulfur cluster. Uracil in DNA can arise as a result of mis-incorporation of dUMP residues by DNA polymerase or via deamination of cytosine. Uracil in DNA mispaired with guanine is one of the major pro-mutagenic events, causing G:C->A:T mutations. Thus, UDG is an essential enzyme for maintaining the integrity of genetic information. UDGs have been classified into various families on the basis of their substrate specificity, conserved motifs, and structural similarities. Although these families demonstrate different substrate specificities, often the function of one enzyme can be complemented by the other.	1.31618e-105
NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	1.57556e-15
NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein	gnl|CDD|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	3.09539e-11
NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein	gnl|CDD|227111	COG4770, COG4770, Acetyl/propionyl-CoA carboxylase, alpha subunit [Lipid metabolism].	0

Protein sequences

>NZ_CP040915.1|WP_139927474.1|1056747_1057911_+|hypothetical-protein
MATTIASQLLEFLMNLMRDPQAAAEFRADPEAALDSAGLADVCSADVDAVMPVVMDHAVKVGSSFGREARDGRDGRDGRDGRDGRDGRDGRDGHGHKDDDKHDRDDDHGHGRDHGHGRDDDDHSHAVQQISHVVNNYSYTSTVDDRDTITDQSVNQNIWAKGDVNQWFDNDAMIASGDDSIAAGGDVDVDNSTNNSINVLAHDSNVEIGNTDVDINDSFNDDHSTDNSDHSTNVINDSFNDNSDNSTNLDVDIDDSFNDESVDVDVDVDDSFNQDNDGVDIEEVDVDDSFNQDNDGIDVEEVDVDVDNSNQDNVTISDNEVGNTEISDNVVIADNEVGNTEITDNVVIEDSFDDNFSNNFTDDDVLDIDDQDFVDVDNTANDNELEL
>NZ_CP040915.1|WP_139931345.1|1054649_1056395_+|helix-turn-helix-transcriptional-regulator
MVAATPTHQVRSRQRALLEAIDVSGRPLNGVASRLARSGIEDPRVAEALVAQGDTLLPRDPAKAFEVYSQAVAAGADHTALAARRAQAAALSGNLDPAGRLVDELLSLPEPPDLGRAVDVAAEVWSRRGMLSRSADVYRWLGPDRIGASAPLAAIALVGCGDRAGMDDMLAAAGPPTSPTLLAAVPTLVCEGLRETLDSASTNAMGSLVRASDMMTASGSTLPMPMNPAALAALVALHLGELAVAESVTEDALAGNQGGAGCRPRLLLMRAWTAMLRDRPDHARAAITEARSAGEVLSPRDELFLRALEVGLARRTDDPPGLVQAWGRARESILHFPVDLFTLLPLGELLVAAARLRDSARIEGHVAEAWALLGRLGDPPLWTVPLHWAEVHAAILAERPGQLGPHAAALVRASGQSHFAAVLAAAGRVWVSVLAGDVDVEAVEIAARGLASVGLTWDGSRLAGHAAARAPERKDMARLLARARDLHPAAALAPEQAPTAPPGSNRSGTLLDDSGLSPREREIAAQVLAGRTYREIGDAIYISPRTVEHHVARIRRRLGASSRSELLARMRIALGEESWTS
>NZ_CP040915.1|WP_139927473.1|1051826_1053857_+|Hsp70-family-protein
MTYSVGVDIGTSFVAAAITRIVDGRPQAPQPLHLGARSTATPSVMYFGDDGQVLVGDAAERRGTTDPDRVVRESKRRIGDSVPVVVGDLLVAPEDIYATMVRWVVDRADEQEGAPPDRVAVAHPVGWGAYKTGLVREALAGVGLGEVELISEPEAAALHYASFERVEVGSTIAVYDLGGGTFDVAILRKAETDTFDVLGRPEGIERLGGADFDEAVFRHVTAGLGEGFTSLDRTDPGVLVALSRMRRECTEAKEALSSDSETVVPVLLPGMQTQVRLVRSEFEELIAASVRETVASVEQALRTAQVEPEDLTAVLLIGGSSRVPLVAQLLSAELGRPIAVDADPKASICLGASLAAAYPGAIEGTAVLLGDDDVTVAPARAQAGDGVAPVTEPPSPAGAALAPAATAFVANAPHQHIGSRRGIKIAAIAGLVASITVFTTVAGQTPEVQELIKSSLRVSEAQAGTPAADGGEAVAAGEDGRGGAGGSGEGASSDRSGVARLNTVAPKPGDPTGKPKPTPTDEASTKVSATGSPTTGVPGTTSTGGKTTPGTNTPGGTATGDGSGTGGAPTGTPDGAGTPTTDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTPSPDPTTEPPPEPEPTATATATATATEESTPPQDPPPPADTPPAEEPPATGAAITVPADPVLG
>NZ_CP040915.1|WP_139927472.1|1050897_1051545_-|septum-formation-inhibitor-Maf
MTTLLLASASPARLSTLRAAGLDPLVAASSVDEAKLLATATTEADRAGSAPVPPADQVLLLARAKAHDVREHPTLAREADVVLGCDSMLELEGEVLGKPTDAADAVVRWQRMRGRTGVLHTGHCLLDRDGREASATSSTVVHFADLTDAEVDAYVATGEPLWVAGAFTVDGLGGPFVAGIEGDYHGVVGVSLPLLRVLLAELGVAITDLWRPAAD
>NZ_CP040915.1|WP_139927471.1|1050024_1050870_+|uracil-DNA-glycosylase
MATVSTAPDLRPHPVTGRLFPSPVPPGTGWPEDPADAGTPVATTVPAVVDLARAAADVGELDARVSVCRACPRLVAWRESVATTGRRASFADQPYWGRPGPGVGDPAPQVLVVGLAPAANGTNRTGRMFTGDRSGDWIYAALYRAGYASQPDSWAAGDGLKLAGARIVAAVRCAPPANKPTPEERRTCGHWLDRDLELAAPGLRSMLALGAIGWDAALASARRLGWTVPRPKPRFGHGAQTELVAADGHPIRLLGSYHVSQQNTFTGRLTEAMLDAVIARL
>NZ_CP040915.1|WP_139927470.1|1047718_1049566_-|ATP-grasp-domain-containing-protein
MTSTSSQLSPRGLTKVLIANRGEIAVRVARACADAGVATVAVYADSDRDALHVKLSDEAFALHGQRAAETYLDAGKILDVARRSGADAVHPGYGFLSENAGFAQAVLDAGLIWIGPPPAAIEALGDKVTARHIAQKVGAPLVPGTPDPVSGAEEVLAFADAHGLPIAIKAAFGGGGRGLKVARTREEIPELYESAVREAVAAFGRGECFVERFLDRPRHVETQCLADAAGNVVVVSTRDCSLQRRHQKLVEEAPAPFLTPAQEQTLVHASQAILREAGYVGAGTCEFLVGQDGTISFLEVNTRLQVEHPVTEEVTGIDLVREQLRLAAGEDLGYTEVATRGHAIELRINGEDPASGFMPAPGTISSLSWPSGPGVRVDSGVVAGDTISGAFDSMLAKIIITGATRTQAIERARRALRETEIVGLPTVVPFHRSVLTEPDFTADDGASSFGVHTTWIETDYAEHLRSLPSTRPAPAVAAPAEEPAEATERVIVEVGGKRLEVVIPAGLGISTGPRGAARRPVRRTVGRSSGTGGTNGAALTSPMQGTIVKVAVGDGEVVAQGDLVVVLEAMKMEQPLVAHRAGRVSGMAAAVGRNVATGAVICQIEPVEQAAPDAG
>NZ_CP040915.1|WP_139927469.1|1046792_1047692_-|NUDIX-domain-containing-protein
MTASASRPPDARVHRQPGDGWVECSCGRRHWGLNGAAGLLLWRTGPAGPQLVLQHRALWSHHGGTWGLPGGALSDGETPVDGAVREAREEAGVVPAGLQVTAARALVHPDWAYTTVLAQATAPFEPAVTDPESLEVRWVDLASIEGFDLLPAFGDALPELRTMLRRLVLVVDAANVVGSRPDGWWADRAGATVRLRDHLAALARDGLDAVAVDLPGQRWYPEVVLVTEGAARGVDPTDGVRVVTAHGSGDDAVVQTVTAVLGATGDGVTDVAVATADRELSARVAALGARTLGPLLVRH
>NZ_CP040915.1|WP_139927468.1|1045761_1046724_-|2,3,4,5-tetrahydropyridine-2,6-dicarboxylate-N-succinyltransferase
MTERTAWAFGLATITDTGDTLEAWYPAPTLGAPPQDAAAPAELSAATSVDASRLVRTEVVRTEIDLDAAPASVADAYLRLHLLSHTLVQPNSINLDGIFGVLPTVVWTSAGPCAVEGFEATRARLRARGVLTVYGVDKFPRMVDYVVPAGVRIADGDRVRLGAHLAPGTTVMHEGFVNFNAGTLGRSMVEGRISQGVVVADGADVGGGASIMGTLSGGGKRVISVGPRSLLGANAGLGISLGADCVVEAGLYLTAGTKVSVIIGGGARPRHGQLDEPAVVSARDLSGRDNLLFRRNSLSGAVEAISRSGTGAELNAALHA
>NZ_CP040915.1|WP_139931343.1|1044668_1045670_-|hypothetical-protein
MGCTGGAVLALGALGVAITGVVLALNTFVHSPASGTCTVALADGGVQRLDADQADNAALFAANAAHRDLPARAVTIAIATALQESKMRNIDYGDRDSVGLFQQRPSQGWGTVEQIMDPVYSTNAFYDVLVTVQGWESQEITDAAQRVQRSGFPLAYAQHEDRGRAFASALSGYSPASLSCHLDPVVEAPDGVGAPGSAGDGESTPTAVVEGTASAGPIAGATPPARLATIQQRLTRDFVDISATVVPAGVLQVDATSLPAGLDPAPARRGWAVAQWAVATASQTGARVVAVDGQVWVRDDGDDAAWLPLAEAGLPAALHDATASAAPGAVLIG
>NZ_CP040915.1|WP_139927467.1|1043525_1044467_-|hypothetical-protein
MNTNEGPELILVRDLTALGRDPRSTQRASRSRALTRVRRGAYADARAWATATNSERHRLFVLSTMAGMRTPPVLSHESAAVLLGIPLMGPPPEKVHVAGDSASGGRSSACIQRHVVRPMPAITLVDGVAVTSAARTVVDLARSRPFTAGLVAADYVLRVGLVARAHLDEALDEVAGQRGARRARAVIDRADARAESVGESLSRAQMHLLGVPIPELQHVFYDADGFIGRTDFWWVEERKVGEFDGRIKYQPPERSGGLPPEKVVWREKRREDRLRRQIEGVVRWVWTEALNTSGFGRLLAGAGIYPVRPGVRP
>NZ_CP040915.1|WP_139927476.1|1059470_1061372_+|Isoniazid-inducible-protein-iniA
MADLVKLVEQTIALVRDGDRADLSRRLEHTRQRLLDPSIRVIVVGEFKQGKSMLINALVGAPVCPVDDDIATAVPTVVRHGAAPSAVVLVPDPGGTDAEPTVQRRPVPLEELPAYVGEAGNPGNVKGLLGAEVTLPRAILAGGLAIIDSPGVGGLDSAHALTTLTALPTADAMLLVSDASQEYTEPEVAFLRQSMRVCPNVAGVLSKTDLYPQWRQVAQIDRGHLAKVDEEIPLFPVSSVLRLQAGRAKSQELNEESGFPGLIGYLRREIVGQAERLQRRSVAQDLRSTAEHLRLSLSSELAALENPEGTPQLLAELEVAKEHADEQRKKSARWQVTLNDGVADLISDMEFDLRDRLRAVQRDAEAAIDAGDPGPVWDQFTDWLEQRVAATVSETFLWTSERSQWLAEQVGALFAQDELRLPVLRVDDTDDVLDPVPLVPDLDAGHLSVTQKVLIGMRGSYGGVLMFGLLTGIAGMALINPISVAAGVLLGGKVYREDKEARLRRRQGEAKSIVRRQIDDVSFQVGKQLRDRLRIVQRTIRDHFTEIAEEHHRSLSDSVVAAQRAASIFSAERDQRIAVLKIDLNRVDALARKADALETADAEAPEPRSARAGRAGTPSRVGRPRGGAVVAEA
>NZ_CP040915.1|WP_139927477.1|1061368_1062889_+|GTP-binding-protein
MSTEGGVRLLLREALEVYADDPVAATSLHGWASRLDGPLRVAIAGMVKAGKSTLLNAILGEELAPTDTGECTRVVTWYRHGATPRVTLYPRDGEPRQLPLRRVEGRLRLDLGGTPAEEVARLVVDWPTAGLRDLTLIDTPGIASLSTDVSARATAFLTPEDSPSEADAVVYLMRHMHGSDIHFLESFRDAEAGRSGTVNALAVLSRADEVGAGRLDSMISARDVARRYREDPSLRPLALSVVPIAGLLAQSARTLRQSEFAALRELAELGREERERLLLSADRFTRAEITPAVDVTMRAALVERLGLFGLRLALVLIRSGLDDPTDLARELARRSGLGELQRLIDGQFQARSAQLKARTALVGLETLLRTRPRPGTERLATELERIQAGAHEFRELRLLGTARTVGLGLPRDLEAEAERLVGGRGVAPARRLNLADGASDAKIRAAALESLRRWRALAENPLTDRSTAGACEVVARSCEALVVAAQPVAGPTTRPQLRPEPARGGG
>NZ_CP040915.1|WP_139927478.1|1062856_1063351_-|hypothetical-protein
MTYQADAPVHREVEAPGALRTSRTLWLLSFVAGLVAVGFSWLNRDDGKQRLLETVTDLAPGRDAATLEALANLVFWGSLGAIALVVVLEALLLRTMMRRRAWPRVAAFFVLVVHAAVMVLAEAYLAAPGGAGAAVRWPLLIQLGLAVVAWIVSLSPAASRWFRA
>NZ_CP040915.1|WP_139931347.1|1063832_1065467_-|DUF885-family-protein
MRRIALDPLEATSLGLPGHDHEMPDLSPAGLAARTDLDRATLAELEAVAPVDGVDRVTHAAMRERLGVAVELADAGELTRELNVIASPVQAVREVFDLMPTATAADWETIAERLRAVPAALDGYQDSLLAARGAGHVAALRQVEACLKQADELADADTSFFTTFTAGAQPDGEAPHRALAAELEAGARDARQAYADLARMLGEELAPDAPELDAVGRERYGLWSRYFLGAVVDLDETYAWGQEDLARVVAEQQAVAEELYGPGTGIREAMDRLDKDPDRMLHGTPALREWMQATSDEAVAALTDAQFDIPEPVRRLECMIAPTQSGGIYYTGPSADFSRPGRMWWSVPAGVTDFATWREKTTVYHEGVPGHHLQIGQTVYRSGLLNMWRRMASWVSGHGEGWALYAERLMADLGFLDDPGDRMGMLDGQRLRAARVVLDIGVHLGKPAPDEWGGGTWDAAKAWPFLKANANMAEGFLAFELDRYLGWPGQAPAYKIGQRLWEEIRDDAGTAARRDGGELDLKAFHRRALDIGSVGLDVLREALV
>NZ_CP040915.1|WP_139931349.1|1065659_1066406_-|methyltransferase-domain-containing-protein
MGRWSRPLAAAFVEWLGAPDGLEWLDVGCGTGAVTAAIVTGAAPSAVLAIDPSPGFVATARRLTASPLARFTVGDAATLPMGDDAVDRCVSGLVVNFLPDASAAVAEMRRVTRRGGWVAAYVWDYAGGMELLREFWAAAVTVDPGAAQMDERHRFPLCAPGPLGELWRSAGLDGVESRPLTVSTHFPDFDDLWAPFLGGQGPAPAYVGSLTPERRPALARELRRRLHPSADGAIELTARAWAVRGRRR
>NZ_CP040915.1|WP_168205775.1|1066692_1066917_-|acyl-CoA-carboxylase-subunit-epsilon
MTSPAVRVLRGRPDEVELAALVAGIVAARGRADELGGLPDEAAECVRSRWSERARVLGMATAPDAGAWRWSLHP
>NZ_CP040915.1|WP_168205599.1|1067060_1068740_-|acyl-CoA-carboxylase-subunit-beta
MTDSSIDLSAPVAGASPAGDSPATPPTAVPAQPPTTAAKVADLAAREQNLTDAAATAVEKQHKRGKKSARERIEALLDPGSFTELDAFATHRSSNFGLDKKRIPGDGVVTGYGTVDGRQVCIYSQDFTVFGGSLGEVHGQKITKVMDMALTTGVPLIGISDGGGARIQEGVAALTQFAEIFRRNVAASGVIPQISLILGPSAGGAVYSPALTDFIVMAEGTSNMFITGPDVIKAVTGEEVGFEELGGAATHNQRSGVAHYQAADEDDAVDYVRALLSYLPSNNLSEPPSWPVSADEAEAALEVTDTDRELDTLVPDSDNQPYDMRVVVEHVLDDHEMLEVQPGYAPNMITAFGHVEGRPVGVVANQPQQMAGTLDINAAEKAARFVRTCDAFNIPVLTFVDVPGFLPGTDQEWNGIIRRGAKLIYAYAEATVPLVTLITRKAYGGAYIVMGSKKLGADVNLAWPTAQIAVMGSGGAVNILQRGALKKVAEEGGDVEAERARLVAEYEETLVNPWEAAERGFVDAVITPADTRVQVVKALRALRTKRASGPAKKHGNIPL
>NZ_CP040915.1|WP_168205600.1|1068858_1069017_-|hypothetical-protein
MYAAIWRRLPGPRWLKALQALTLVAAVTAALFVWVFPAVTTGLGLFETTVAG
>NZ_CP040915.1|WP_139927479.1|1069016_1069784_-|class-E-sortase
MTRLTGAAAPPAPRAVTAPVSAHRGASVLGELLITAAAVLALFVVWQVWWTDVTGGRAQVAAVVAIETSFPTVPATPADSPASPLRTDAPPTLAEVPAGTGFAVVHVPRWGTDHALPVLEGVDARAVLDTGAAGHYPGTAPPGAVGNFALAAHRQTYGAAFRRVDELRVGDPIVVETAEAWLVYRVTADRVVAPEEVSVIAPVPGAPGEAATARMITFTTCHPLWSTAQRWVTHGELAGWLPRAAGVPAELGEVA
>NZ_CP040915.1|WP_139927480.1|1069862_1070777_+|biotin--[acetyl-CoA-carboxylase]-ligase
MPDDASPLPPFTRVVRVVQTGSTNTDLREAVTAEPGAWPHLSVLVAETQDAGRGRAGRSWDTAPGTALTASVLLRPRVPPGRLPWLTLLAGLAVQRATAELTGVRTGLKWPNDVLVLDVGEEVDGWGTDRKVAGILAEALPAADSHDAGPHAAGPHAAGPHAAGPHAGAGHAGSLAVVLGIGVNVAQTRDQLPVPWATSLRLAADARVTTPGAEELLSAVGRHLADLLRRWEAAAGDAGAAGLAEDVARVCVTLGRSVRAELPGGIEVTGTATALDNDGHLLLRTPEGTERTVRAGDVRHVRAG

Crispr_ID: NZ_CP040915_7

• CRISPR_ID: NZ_CP040915_7
• CRISPR_location: 1313364-1313457
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_7

Consensus_repeat	Method
GCCCGCACCACGGGCGCCGAGAA	CRISPRCasFinder

spacers of NZ_CP040915_7

>7.1|1313387|48|NZ_CP040915|CRISPRCasFinder
CCGGCACGCCCAGCCCGCACCACGGGCGTGGAGAAGCCGGCACACCCC

CRISPR arrays and Neighbor proteins around NZ_CP040915_7

CRISPR arrays

The CRISPR arrays of NZ_CP040915_7

>merge|NZ_CP040915|7|1313364-1313457|CRISPRCasFinder
GCCCGCACCACGGGCGCCGAGAACCGGCACGCCCAGCCCGCACCACGGGCGTGGAGAAGCCGGCACACCCCGCCCGCTCCACGGGCGCCGAGAA

>NZ_CP040915|7|7|1313364-1313457|CRISPRCasFinder
GCCCGCACCACGGGCGCCGAGAA	CCGGCACGCCCAGCCCGCACCACGGGCGTGGAGAAGCCGGCACACCCC
GCCCGCTCCACGGGCGCCGAGAA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139927675.1|1310328_1312008_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	unknown	unknown	gnl|CDD|223362
NZ_CP040915.1|WP_139927679.1|1315312_1316014_-|DUF998-domain-containing-protein	unknown	unknown	gnl|CDD|377627
NZ_CP040915.1|WP_139927671.1|1303668_1305018_-|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|377028
NZ_CP040915.1|WP_139931410.1|1301180_1301915_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223673
NZ_CP040915.1|WP_139931414.1|1316958_1317381_+|nucleoside-diphosphate-kinase	unknown	unknown	gnl|CDD|239876
NZ_CP040915.1|WP_139927678.1|1314098_1314848_+|PTS-dependent-dihydroxyacetone-kinase-phosphotransferase-subunit-DhaM	unknown	unknown	gnl|CDD|131417
NZ_CP040915.1|WP_139927670.1|1303236_1303620_-|SnoaL-like-domain-containing-protein	unknown	unknown	gnl|CDD|378915
NZ_CP040915.1|WP_139927676.1|1312320_1313322_+|dihydroxyacetone-kinase-subunit-DhaK	unknown	unknown	gnl|CDD|237724
NZ_CP040915.1|WP_139927680.1|1316028_1316793_-|type-I-methionyl-aminopeptidase	unknown	unknown	gnl|CDD|238519
NZ_CP040915.1|WP_139927684.1|1322404_1323583_+|signal-recognition-particle-docking-protein-FtsY	unknown	unknown	gnl|CDD|236686
NZ_CP040915.1|WP_139927681.1|1317387_1317996_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139931413.1|1314949_1315303_+|DUF4233-domain-containing-protein	unknown	unknown	gnl|CDD|379420
NZ_CP040915.1|WP_139927674.1|1307059_1310329_+|isoleucine--tRNA-ligase	unknown	unknown	gnl|CDD|235681
NZ_CP040915.1|WP_139927668.1|1299034_1300060_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223673
NZ_CP040915.1|WP_139927683.1|1321979_1322291_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139927672.1|1305106_1305928_-|pyrroline-5-carboxylate-reductase	unknown	unknown	gnl|CDD|223422
NZ_CP040915.1|WP_139927669.1|1301962_1303123_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|378117
NZ_CP040915.1|WP_139927673.1|1306130_1306721_-|hypothetical-protein	unknown	unknown	gnl|CDD|225753
NZ_CP040915.1|WP_139927682.1|1318295_1321934_+|chromosome-segregation-protein-SMC	unknown	unknown	gnl|CDD|274008
NZ_CP040915.1|WP_139927677.1|1313466_1314102_+|dihydroxyacetone-kinase-subunit-L	unknown	unknown	gnl|CDD|274099

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139927675.1|1310328_1312008_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase	gnl|CDD|223362	COG0285, FolC, Folylpolyglutamate synthase [Coenzyme metabolism].	3.09952e-129
NZ_CP040915.1|WP_139927679.1|1315312_1316014_-|DUF998-domain-containing-protein	gnl|CDD|377627	pfam06197, DUF998, Protein of unknown function (DUF998). Family of conserved archaeal proteins.	3.71685e-08
NZ_CP040915.1|WP_139927671.1|1303668_1305018_-|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	1.38909e-10
NZ_CP040915.1|WP_139931410.1|1301180_1301915_+|ABC-transporter-permease-subunit	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	4.55162e-42
NZ_CP040915.1|WP_139931414.1|1316958_1317381_+|nucleoside-diphosphate-kinase	gnl|CDD|239876	cd04413, NDPk_I, Nucleoside diphosphate kinase Group I (NDPk_I)-like: NDP kinase domains are present in a large family of structurally and functionally conserved proteins from bacteria to humans that generally catalyze the transfer of gamma-phosphates of a nucleoside triphosphate (NTP) donor onto a nucleoside diphosphate (NDP) acceptor through a phosphohistidine intermediate. The mammalian nm23/NDP kinase gene family can be divided into two distinct groups. The group I genes encode proteins that generally have highly homologous counterparts in other organisms and possess the classic enzymatic activity of a kinase. This group includes vertebrate NDP kinases A-D (Nm23- H1 to -H4), and its counterparts in bacteria, archea and other eukaryotes. NDP kinases exist in two different quaternary structures; all known eukaryotic enzymes are hexamers, while some bacterial enzymes are tetramers, as in Myxococcus. They possess the NDP kinase active site motif (NXXH[G/A]SD) and the nine residues that are most essential for catalysis.	4.85302e-74
NZ_CP040915.1|WP_139927678.1|1314098_1314848_+|PTS-dependent-dihydroxyacetone-kinase-phosphotransferase-subunit-DhaM	gnl|CDD|131417	TIGR02364, dha_pts, dihydroxyacetone kinase, phosphotransfer subunit. In E. coli and many other bacteria, unlike the yeasts and a few bacteria such as Citrobacter freundii, the dihydroxyacetone kinase (also called glycerone kinase) transfers a phosphate from a phosphoprotein rather than from ATP and contains multiple subunits. This protein, which resembles proteins of PTS transport systems, is found with its gene adjacent to.	1.49667e-31
NZ_CP040915.1|WP_139927670.1|1303236_1303620_-|SnoaL-like-domain-containing-protein	gnl|CDD|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	1.09038e-09
NZ_CP040915.1|WP_139927676.1|1312320_1313322_+|dihydroxyacetone-kinase-subunit-DhaK	gnl|CDD|237724	PRK14481, PRK14481, dihydroxyacetone kinase subunit DhaK; Provisional.	0
NZ_CP040915.1|WP_139927680.1|1316028_1316793_-|type-I-methionyl-aminopeptidase	gnl|CDD|238519	cd01086, MetAP1, Methionine Aminopeptidase 1. E.C. 3.4.11.18. Also known as methionyl aminopeptidase and Peptidase M. Catalyzes release of N-terminal amino acids, preferentially methionine, from peptides and arylamides.	4.785e-107
NZ_CP040915.1|WP_139927684.1|1322404_1323583_+|signal-recognition-particle-docking-protein-FtsY	gnl|CDD|236686	PRK10416, PRK10416, signal recognition particle-docking protein FtsY; Provisional.	7.91631e-157
NZ_CP040915.1|WP_139931413.1|1314949_1315303_+|DUF4233-domain-containing-protein	gnl|CDD|379420	pfam14017, DUF4233, Protein of unknown function (DUF4233). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 122 and 147 amino acids in length. Proteins in this family are integral membrane proteins.	1.18734e-15
NZ_CP040915.1|WP_139927674.1|1307059_1310329_+|isoleucine--tRNA-ligase	gnl|CDD|235681	PRK06039, ileS, isoleucyl-tRNA synthetase; Reviewed.	0
NZ_CP040915.1|WP_139927668.1|1299034_1300060_+|ABC-transporter-permease-subunit	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	2.9802e-31
NZ_CP040915.1|WP_139927672.1|1305106_1305928_-|pyrroline-5-carboxylate-reductase	gnl|CDD|223422	COG0345, ProC, Pyrroline-5-carboxylate reductase [Amino acid transport and metabolism].	3.16316e-85
NZ_CP040915.1|WP_139927669.1|1301962_1303123_+|ABC-transporter-substrate-binding-protein	gnl|CDD|378117	pfam09084, NMT1, NMT1/THI5 like. This family contains the NMT1 and THI5 proteins. These proteins are proposed to be required for the biosynthesis of the pyrimidine moiety of thiamine. They are regulated by thiamine. The protein adopts a fold related to the periplasmic binding protein (PBP) family. Both pyridoxal-5'-phosphate (PLP) and an iron atom are bound to the protein suggesting numerous residues of the active site necessary for HMP-P biosynthesis. The yeast protein is a dimer and, although exceptionally using PLP as a substrate, has notable similarities with enzymes dependent on this molecule as a cofactor.	6.15865e-29
NZ_CP040915.1|WP_139927673.1|1306130_1306721_-|hypothetical-protein	gnl|CDD|225753	COG3212, COG3212, Predicted membrane protein [Function unknown].	1.30499e-06
NZ_CP040915.1|WP_139927682.1|1318295_1321934_+|chromosome-segregation-protein-SMC	gnl|CDD|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0
NZ_CP040915.1|WP_139927677.1|1313466_1314102_+|dihydroxyacetone-kinase-subunit-L	gnl|CDD|274099	TIGR02365, dha_L_ycgS, dihydroxyacetone kinase, phosphoprotein-dependent, L subunit. Two types of dihydroxyacetone kinase (glycerone kinase) are described. In yeast and a few bacteria, e.g. Citrobacter freundii, the enzyme is a single chain that uses ATP as phosphoryl donor and is designated EC 2.7.1.29. By contract, E. coli and many other bacterial species have a multisubunit form (EC 2.7.1.-) with a phosphoprotein donor related to PTS transport proteins. This family represents the subunit homologous to the E. coli YcgS subunit.	4.28738e-74

Protein sequences

>NZ_CP040915.1|WP_139927676.1|1312320_1313322_+|dihydroxyacetone-kinase-subunit-DhaK
MKKLINNPQNVVAESLRGFGLAHPEHVRVNEDPLFVSRAGGAVQGKVGLVSGGGSGHEPLHAGYVGVGMLDAAVPGPMFTSPTPEPILEATKAADGGAGVLHIVKNYTGDVLNFETAAELAEAEDITVKAVIVNDDVAVEDSLYTAGRRGVAGTVLVEKIAGAAAERGDDLDAVVAVAQKVIDNVRSMGVALSACTVPHAGKPSFDLEEDEIEIGIGIHGEPGRHRIAMAGADEITERLLTPVLEDLKVTDGEEVLLFVNGMGGTPLSELYVVYNHARDLLDQRGLKVTRSLVGNYITSLEMQGASVTVLRLDADLTALWDAPVDTPALRRGL
>NZ_CP040915.1|WP_139927675.1|1310328_1312008_+|bifunctional-folylpolyglutamate-synthase/dihydrofolate-synthase
MDQRTPGDVPEETGAAGPGPAGAARRDPAEAEREAQERIAAFMAAADAPDDGVDPVSDTTTEEDEHAAGLRALLGSALFTGPDPDVAEEVLHEEEAEPSDAQKHAVAVAHAQAEEQVRGIYLDILARAPEHDVQPSLQRVADVLELLGDPHRAYPVIHLTGTNGKTSTARMIERLLREKGLRTGRFTSPHLHSVRERIALDGAPISPEAFVATWEDVKPYIEMVDARSQADGGPRLSFFEVFTVMAYAAFADAPVDVAVVEVGMGGRWDATNVADGTVEVLTRIDRDHERWLGHTLEEIAGEKVGIITDRSTVLSAAQQEEVESVIMSAAAQHGARLLRDGQDLAVVDRQLGVGGQLLTLSTPAGVYQDVFLPLHGEHQAHNALLALAAVETFFGGAALDGGVVEQGFAGVDSPGRLELVRRSPTVLVDAAHNPAGIDALRAAIEEAFPFSHLVGVVGVMADKDAEGILAGLEPLLAEIVVTRATTDRAMDVEELAEIAADVFGEERVHVAERLDDAIDKAATLAEADPEEVVTSTGILVAGSVILAAEARALMGRKTA
>NZ_CP040915.1|WP_139927674.1|1307059_1310329_+|isoleucine--tRNA-ligase
MADQPQRYPLHRPGSEVVASPSFPALEQEVLEYWKRDDTFQASIDNRDAGTDGEGEFVFYDGPPFANGLPHYGHLLTGYVKDVVGRFQTQIGHRVERRFGWDTHGLPAELEAERILGIKDKSEIEAMGIEAFNKACRDSVLKYTNEWQDYVTRQARWVDFDNDYKTLDTTFMESVIWAFKQLYDKGLAYEGYRVLPYCWHDQTPLSNHELRMDDDVYQMRQDPSVTVGVRLETGELALIWTTTPWTLPSNLAVAAGPEIDYVTVAPAEGPLAGERVILAKSRLHAYARELGEEPDVVATYPGTELVGRRYAPIFDYFVGRPDDEAPGPNAWQVVAAEYVTTEDGTGLVHQAPAFGEDDMAVCQANGIGTVVPVDDGGRFTTEVPDYAGSQVFEANKAIIADLKHGTGPLARRPQAERAVLVRQETYDHSYPHCWRCRTPLIYKAVTSWFVRVSEFRDRMVELNQDITWVPEHIKEGQFGHWLAGARDWSISRNRYWGTPIPVWVSDDPAHPRIDVYGSLAELEADFGRLPLDRDGEPNLHRPFIDELTRPNPDDPTGQSTMRRIPDVLDVWFDSGSMPYAQVHYPFENRDWFEHHNPGDFIVEYIGQTRGWFYTLHVLATALFDRPAFRTSVSHGIVLGSDGRKMSKSLRNYPDVTEVLDRDGSDAMRWFLMSSPILRGGNLVVTEEGIRENVRQILLPLWNTWYFFALYAGTVDGGRGYLARPVALDDAAEVAGLHVMDRYLLARTRDLAAQVKDQLERYDVPGATQSVREHLDLLTNWYVRTSRDRFWAEDAGAFNTLYTALEVLTRVMAPLAPLVSEEIWRGLTGGRSVHLTDWPALPATVADPELVGAMDQVRDAVSATLGLRKANARRVRQPLRTLTVVVDAPGALTPFTGLIATEVNVKDVDVRALGDGAAEQFGVVTKLTVNARAAGPRLGKDVQRAIRAARDGFWEQREGGDGAPTVVVDGIELKAEEFTLTTEVAGGEDGSAVAGMLPGGGFVVLDIAVDDELAAEGYARDVVRLVQDERKATDLYVADRIHLDLVVPADKLEWVQTHRDLVARETLALEVRVVAGDVETPQIRVEKVDA
>NZ_CP040915.1|WP_139927673.1|1306130_1306721_-|hypothetical-protein
MDRRRAAAAAATVLLLAGCGSTREEVPLPGIEQSPAGEADTPSASPGTPSPSPTADDGADADAAATGDAALTAVRTAENAVPGGRAADLDRDDDDGDYEITVVGAGGAEDVAVGSDGTQVLRQQPDDDLDDDDRAALGTATVTLADAIDAAVAQSGGVVDDVELETEDNGVVWKVKVRAGDGEREVRVDAADGTVR
>NZ_CP040915.1|WP_139927672.1|1305106_1305928_-|pyrroline-5-carboxylate-reductase
MRVGFIGAGNMAGAIVRGIVASGSLAPEDVVVTSAHGHSAQALARETGVDVVDTNDELVEQVGAGGVVVLAVKPHMIADVLAPLQDLLAEQGSLVVSLAAGTTLDRLAELLPEGQAVVRVMPNVNAQIGAGMAAVCGNAEASENQVDAVVGLFENVGRAIVLPERDFAAYSAIAGASPAFVFTFIDALARGGVKNGLAKAQAVRIAAQAVLGSARMVLERAADGATPADLVDTVTSPGGTTVAGLVAMEDAGFSPAVVRGVQATVDRDRELGA
>NZ_CP040915.1|WP_139927671.1|1303668_1305018_-|endonuclease/exonuclease/phosphatase-family-protein
MRVQAGALGALGVAAVVAAGLAVPAAAEPTARPDDRSTLRVATFNASLNRAAEGQLAADLATGADAQARAVAEIIRLTAPDVVLLNEFDDDPTGQAVRDFREKYLQAGLVAGGAAPVDYPYVYTGLAETRDDTESGDTGLGVTAPEDAAPPTVPFNTGLPSGHDLDNDGVVGSPGTPEGASDALGFGTFPGQYGMVVLSRYPIDTDRVRTFQSFLWRDMPGALLPDDPATPAAADWYAPEELDVLPLSSKSHWDVPVQVGNTTVHVLAAHPTPPSFDGPEDRNGRRNHDEIRFWADYVSGGRADDYIYDDAGRTGGLTPGARFVVTGDYNADPLDGDSVPGAIDQLLDHRRVRDPRPTSGGAVEAAATQRGANVAHRGDPARDTADFDDTAPGNLRVDYVLPSRNLPVRGAGVFWPMADEPGSELTGQFPSPSSDHRLVWVDVRVPGLR
>NZ_CP040915.1|WP_139927670.1|1303236_1303620_-|SnoaL-like-domain-containing-protein
MGENENRAVVERLVQCLNDKRVEVMDELFHEDAVMDWPQSGEQVIGGDNRRAVYGAFPGLPTVTPRRVLSAGDLVVLEATLDYGGPAYNSVFVFEMREGRIARETAYWAEPFEAPEWRAAWVTRAQT
>NZ_CP040915.1|WP_139927669.1|1301962_1303123_+|ABC-transporter-substrate-binding-protein
MRLTKLSAGVAAAAAASLLLAACGDSGDPAAPGDDATSEAGGELTPVSLQLQWFIQGQFAGYLAADALGYYEDAGLDVEIVEGGVDIVPQAVLADGTVDYAIAWVPKALASREQGAGITNVAQIFERSGTLQVAWADSGISASADLAGKKVGNWGFGNEFELFAGMTGAGLDPATDVTLVQQQFDMNALLAREIDAAQAMTYNEYAMLLEAENPDTGELYTADDFTAIDWNDEGVAMLQDAVWANTERLEGDADYQATTVAFLTASLRGWIHCRDNVEECRDITVAAGSQLGNSHQAWMVNEINKLIWPSTNGIGTIDKAMWDQTVEIAMTAQNDQGATVLTREPEGLAYTNDYVEQALEALKADGEDVMGEGYKPIEVELAAGGN
>NZ_CP040915.1|WP_139931410.1|1301180_1301915_+|ABC-transporter-permease-subunit
MLLGVLGLAAWEWLVLAADLKPYLLPSPTAIGAELVASGRLVLDDTLSTGWNVLVGLVAGAVAGVVVALAAARSRLLDGVVSPLAAAAAVMPIVALAPVLNNMFGSTTEVSRQIIVSVVAFAPVFFNTLKGLRQVRPVHRDLMRAYAASGWQVARTVTLPGAVPYVFTGLRLASAVAVIAAVVAEYFGGRQNGLGSAITSAAAASAYPRAWAYVVGAIVLGLVFYCVTLLLERLVARRMGGAVA
>NZ_CP040915.1|WP_139927668.1|1299034_1300060_+|ABC-transporter-permease-subunit
MSTPPARAARSAPDGLVPDVAAAVSAEPGVPGATPVPGGSRSPNRWPWAGGSWPRWVRTAVLGIAGVLMLALVWELYKLLGPVEGVSVGETRVLPRTDERSMPHVWEMVSRLFQPATGAPGAPPLLVPLLSASVFTLAVAMLGWFVGVVVGAALAVLMLRWRLAESAVLPWVILSQTVPLVALAPLVVGWGGRIHIGSLEWERWMSVAAISAYLSFFMVAVGTLRGLKAPDAVHVDLFRSYAVGWWRTLVRLRLPAAVPFLLPALRLAAATSIVGAIVAEVSTGTAGGIGRLIISYAQSASGDPPKPWTAIFAAAALGLVAAGLVSLVGTGLRRYRFSEVS
>NZ_CP040915.1|WP_139927677.1|1313466_1314102_+|dihydroxyacetone-kinase-subunit-L
MTATLGTEWALDWVARAATAVSEHRIDLIELDRAIGDGDHGENMDRGFTAVTAKLAATRPESAGEVLKTVATTLMSTVGGAAGPLYGTAFLRGAKAADGELDAAGVAAVLEAALEGIKARGKAETGEKTMVDAWTPAAEAARAAADAGRSPVEALRAAADAAAAGADATVPMVATKGRASYLGERSAGHRDPGAESSSLLLAAAAEAAEAR
>NZ_CP040915.1|WP_139927678.1|1314098_1314848_+|PTS-dependent-dihydroxyacetone-kinase-phosphotransferase-subunit-DhaM
MTAKAGLVVVSHSVRLAEGVVEVAAQMAPDVPMRAAGGTEDGRVGTSFDKVEAAVSALLGEVEQVVLLTDLGSATMTAESVLDVLDADVADRVVLADGPLVEGAVAGAVAAQSGADAAAVARAVAEAASSFAGAAGGPGDAGATGQPGTAPAQQRAAGNGAGDGEALTATLTLRNKVGLHARPAALLARLVAGFDAEVTVNDVEAASVLALMGLGLEQGDEMHVRARGAQASDALEAVTVAVADGFGEE
>NZ_CP040915.1|WP_139931413.1|1314949_1315303_+|DUF4233-domain-containing-protein
MFAMTVLVSEVFIVLFASLVAHGLRLADLGLIWGVGGAAMLACAVCAGLLRHRAGYVLGSVVQVLLLAAGFLLPMMFVIGVIFGVLWVASVQLGGRIDVERKQRYAAEVEHFRSQSA
>NZ_CP040915.1|WP_139927679.1|1315312_1316014_-|DUF998-domain-containing-protein
MGARAAARRLLAGGVVAGPLFLGSVGAQMLLRDGFDVRRHGLSLLSHGDLGWVQISTFVVTGLLVEGLAVGLHLAPDRWGGAGPAQAMGAAGVGLILAGMFRVDAYGDFPPGLVHDAGARPGGAERVLHSAHGVLHGTEGVLHDVGTALAINAALVACVLLARRFARSGRRGWAGYCSGTAVVGAVLAWWPWGATSVRLVLVSLVLMVWVALVSARLRGVVVDHAPQSELRPR
>NZ_CP040915.1|WP_139927680.1|1316028_1316793_-|type-I-methionyl-aminopeptidase
MIDLKAPTEIDAMRPAGAFVADVLRALGEAADVGVNLLDLETLAHQMIREVGAESCYVDYHPSFGGSPFGHVLCTSINDAVLHGLPSDYRLRDGDLLSVDFAASVDGWVADSALSLVVGTPREQDLQLIAATEEALARAIEVAVVGNKVGDISATIGAVAREHGYLVNTQFGGHGVGRTMHGEPHVPNDGRAGRGYPLQPGLVIAIEPWFLAGTDEIYTDADGWTLRSADGSRGAHSEHTVAVTECGPVVLTGR
>NZ_CP040915.1|WP_139931414.1|1316958_1317381_+|nucleoside-diphosphate-kinase
MATERTLVIVKPDGVARHLIGEVLRRVEAKGYRTVALELRTADADLLAQHYAEHEGKPFFAPLIEFMMSGPVVAAIVEGHGVIEGFRSLAGTTNPTSAAPGTIRGDLGREWGTAVVQNLVHGSDSPESAAREIGLWFPGL
>NZ_CP040915.1|WP_139927681.1|1317387_1317996_-|hypothetical-protein
MPGVVPVELVLGRSAQAVVVLTEMRAYPTGVGLAVGVRLHRDAPRGARNSPDRPGSPDSPDTLLDMDGPETGVDVDGPTGPAAAAEWRAARLVWEMELADGRRVTSAGPDPYRQLIEHGRGSVDWAPDHPVLARRSGVSHADRAERDYWLWPLPPPGPLRVVCRWPARDIETTVGDLDADVIRDAAARARPLWPDPGVGERS
>NZ_CP040915.1|WP_139927682.1|1318295_1321934_+|chromosome-segregation-protein-SMC
MLPFVHLKTLTLRGFKSFASATTLHLEPGITCVVGPNGSGKSNVVDALAWVMGEQGAKTLRGGSMADVIFAGTSSRAPLGRAEVSLTIDNTDGLLPIEYTEVTISRTLFRSGGSEYAINGTPCRLLDIQELLSDTGMGKEMHVIVGQGRLDSVLQASAEERRGFIEEAAGVLKHRRRKEKALRKLEAMQANLARVNDLSAEIRRQLGPLARQADVARRAQVVQADLRDARARLLADDLVQLTAALAQDVADETAVRERKAHVEAAQADARARLAVLEQAAAAAAPRLGQVTDVWYQLSGLRERLRSLGNVASERCRLLGAPSTAEPAPGRDPAELDARAAAAREEEEALQARLEEARAALEARTAERTTAEEAEREAERALAAVHRGVADRREGLARLTGQVSARRSRLEAGEAELGRLRATLTAAQERAATAHAEFTALEQQVAGVEEGEEGLDEAHEAATAELEDAEQAVTALVEAERAAEAERATAAARRDTFALSLRRKDGTGALLDSGLPGLLGPVPEHVSVTPGWENALAAALGPLAEAAVAESVDVAVDAVRQARDRDGGQVRLVLAGAPTPADDGAPTPADDGEAPPAGATWAAELVTVPDPAVRATLMRLLAGVVVVEDLADARRVLTDAPTLTAVTRAGDVLSATAAHGGAPGAPSVLELHAAHEEAVAAVDDAAARVERARFALGPARERVDAARTGARATLEDLHASDARLTAVAERLGRLGSTLRGAEAEAERTRPAIARVEGEVTEHAAELAALAERLEIAQREPEQAEDDLTGATAARDAATEIARSARTAETDARLALRTLEEQAKALSGRAASLAAAARAEREARRRAAEREARRVAQARVAAEVREGAGRALAAIEGSVAAAAASREDAEHERAEREETLTAVRTELEEIAADLATLTDAAHRDEVARAEQRLRISQLEERAVADLGLDPQVLVDDFGPDRPVPATAPVADGEEPAEARPYVRAEQEKRLRAAERDLTRLGKVNPLALEEHAALAERHKFLTDQLADLKKSRADLMQIVREVDDRVERVFAEAFADTAAQFEQVFPRLFPGGEGRLVLTDPDDLLTTGIEIEARPAGKKVKRLSLLSGGERSLTAVALLVSIFKARPSPFYVMDEVEAALDDVNLGRLLEIFTELRASSQLIVITHQKRTMEVADALYGVTMRGDGVTTVISQRLEREPEPAGGEQPHRHVSGS
>NZ_CP040915.1|WP_139927683.1|1321979_1322291_+|hypothetical-protein
MTGAMLAMVGAALCAVVVLLLVLGERRPDGGWYAWLRDSVQAWRSDELAAAKLQPQGSAVRDTPLEDLFSLGAARDQPAYARPEELRDRLDQARQQARSLARR
>NZ_CP040915.1|WP_139927684.1|1322404_1323583_+|signal-recognition-particle-docking-protein-FtsY
MTDQAWILIAVAVVVVVVAVVGVIALTSGRRASRGPSTTLPPAEVSPYEVDQAPGAGASAPEAPASETEAPAVATPTLERPAPAAGRMQRLRARLARSGALGQTLLSILSRGELTESDWEEIEETLLLADVGVGPTTELMDKLRTETKVLGTTDPEHVRDVLRRELLQLVDPTMDRELHLEPVVGDDGEPHPVTMLVVGVNGTGKTTTVGKLARVLVAEGHHVVLGAADTFRAAAADQLSTWGSRVGVPVVRSDREGADPAAVAFDAVKEGRRTGADVVLVDTAGRLQNKAGLMDELGKIKRVMSREAPVREVLLVLDATTGQNGMRQAQVFAEAVDVTGIVLTKLDGTAKGGIVVAVQRELGVPVKFVGLGEGPDDLAPFVAEEFVDALLS

Crispr_ID: NZ_CP040915_8

• CRISPR_ID: NZ_CP040915_8
• CRISPR_location: 2139837-2139964
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040915_8

Consensus_repeat	Method
AGCTCGGCCATGTCGCCACGCTCGCCAGCAAGCTCGATCAGCTG	CRISPRCasFinder

spacers of NZ_CP040915_8

>8.1|2139881|40|NZ_CP040915|CRISPRCasFinder
ATCCACCGCATCGCGGCTGCCTGCGTCGGCAAGGCGACGT

CRISPR arrays and Neighbor proteins around NZ_CP040915_8

CRISPR arrays

The CRISPR arrays of NZ_CP040915_8

>merge|NZ_CP040915|8|2139837-2139964|CRISPRCasFinder
AGCTCGGCCATGTCGCCACGCTCGCCAGCAAGCTCGATCAGCTGATCCACCGCATCGCGGCTGCCTGCGTCGGCAAGGCGACGTAGCTCGGCCATGTCGCCACGCTCGCCAGCAAGCTCGACCAGCTG

>NZ_CP040915|8|8|2139837-2139964|CRISPRCasFinder
AGCTCGGCCATGTCGCCACGCTCGCCAGCAAGCTCGATCAGCTG	ATCCACCGCATCGCGGCTGCCTGCGTCGGCAAGGCGACGT
AGCTCGGCCATGTCGCCACGCTCGCCAGCAAGCTCGACCAGCTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139928595.1|2138385_2138784_+|DUF2695-domain-containing-protein	unknown	unknown	gnl|CDD|378505
NZ_CP040915.1|WP_139931510.1|2148153_2148945_-|esterase-family-protein	unknown	unknown	gnl|CDD|223700
NZ_CP040915.1|WP_139931509.1|2142683_2145065_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223256
NZ_CP040915.1|WP_139928582.1|2131146_2132946_-|2-oxoglutarate-dehydrogenase,-E2-component,-dihydrolipoamide-succinyltransferase	unknown	unknown	gnl|CDD|200219
NZ_CP040915.1|WP_139928597.1|2138867_2139098_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139931508.1|2141317_2142457_+|RNA-polymerase-subunit-sigma-24	unknown	unknown	gnl|CDD|227277
NZ_CP040915.1|WP_139928593.1|2137370_2138270_+|hypothetical-protein	unknown	unknown	gnl|CDD|223156
NZ_CP040915.1|WP_139928603.1|2140904_2141312_+|hypothetical-protein	unknown	unknown	gnl|CDD|226318
NZ_CP040915.1|WP_139928605.1|2145246_2145657_-|VOC-family-protein	unknown	unknown	gnl|CDD|319924
NZ_CP040915.1|WP_139928607.1|2145662_2146112_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_CP040915.1|WP_139928616.1|2148994_2149600_-|biotin-transporter-BioY	unknown	unknown	gnl|CDD|224187
NZ_CP040915.1|WP_168205653.1|2146294_2146771_-|CHRD-domain-containing-protein	unknown	unknown	gnl|CDD|377837
NZ_CP040915.1|WP_139928587.1|2134553_2134871_+|oxidoreductase	unknown	unknown	unknown
NZ_CP040915.1|WP_139928599.1|2139094_2139514_+|PIN-domain-containing-protein	unknown	unknown	gnl|CDD|272863
NZ_CP040915.1|WP_139928589.1|2134925_2136401_-|leucyl-aminopeptidase	unknown	unknown	gnl|CDD|234863
NZ_CP040915.1|WP_139928614.1|2147691_2148087_-|VOC-family-protein	unknown	unknown	gnl|CDD|319924
NZ_CP040915.1|WP_139928584.1|2132970_2134350_-|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl|CDD|235798
NZ_CP040915.1|WP_139931507.1|2136904_2137300_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139928612.1|2146919_2147702_-|putative-protein-N(5)-glutamine-methyltransferase	unknown	unknown	gnl|CDD|274733
NZ_CP040915.1|WP_139928591.1|2136446_2136800_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139928595.1|2138385_2138784_+|DUF2695-domain-containing-protein	gnl|CDD|378505	pfam10905, DUF2695, Protein of unknown function (DUF2695). This bacterial family of proteins has no known function.	1.49791e-16
NZ_CP040915.1|WP_139931509.1|2142683_2145065_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223256	COG0178, UvrA, Excinuclease ATPase subunit [DNA replication, recombination, and repair].	0
NZ_CP040915.1|WP_139928582.1|2131146_2132946_-|2-oxoglutarate-dehydrogenase,-E2-component,-dihydrolipoamide-succinyltransferase	gnl|CDD|200219	TIGR02927, putative_dihydrolipoamide_acyltransferase, 2-oxoglutarate dehydrogenase, E2 component, dihydrolipoamide succinyltransferase. This model represents an Actinobacterial clade of E2 enzyme, a component of the 2-oxoglutarate dehydrogenase complex involved in the TCA cycle. These proteins have multiple domains including the catalytic domain (pfam00198), one or two biotin domains (pfam00364) and an E3-component binding domain (pfam02817).	0
NZ_CP040915.1|WP_139928593.1|2137370_2138270_+|hypothetical-protein	gnl|CDD|223156	COG0078, ArgF, Ornithine carbamoyltransferase [Amino acid transport and metabolism].	2.48889e-78
NZ_CP040915.1|WP_139928603.1|2140904_2141312_+|hypothetical-protein	gnl|CDD|226318	COG3795, COG3795, Uncharacterized protein conserved in bacteria [Function unknown].	3.23032e-14
NZ_CP040915.1|WP_139928605.1|2145246_2145657_-|VOC-family-protein	gnl|CDD|319924	cd07263, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	2.90957e-44
NZ_CP040915.1|WP_139928607.1|2145662_2146112_-|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	3.19082e-27
NZ_CP040915.1|WP_139928616.1|2148994_2149600_-|biotin-transporter-BioY	gnl|CDD|224187	COG1268, BioY, Uncharacterized conserved protein [General function prediction only].	1.31319e-29
NZ_CP040915.1|WP_168205653.1|2146294_2146771_-|CHRD-domain-containing-protein	gnl|CDD|377837	pfam07452, CHRD, CHRD domain. CHRD (after SWISS-PROT abbreviation for chordin) is a novel domain identified in chordin, an inhibitor of bone morphogenetic proteins. This family includes bacterial homologs. It is anticipated to have an immunoglobulin-like beta-barrel structure based on limited similarity to superoxide dismutases but, as yet, no clear functional prediction can be made. Its most conserved feature is a GE[I/L]RCG[V/I/L] motif towards its C-terminal end Most bacterial proteins in this family have only one CHRD domain, whereas it is found repeated in many eukaryotic proteins such as human chordin and Drosophila SOG..	8.45179e-30
NZ_CP040915.1|WP_139931508.1|2141317_2142457_+|RNA-polymerase-subunit-sigma-24	gnl|CDD|227277	COG4941, COG4941, Predicted RNA polymerase sigma factor containing a TPR repeat domain [Transcription].	2.17014e-86
NZ_CP040915.1|WP_139928599.1|2139094_2139514_+|PIN-domain-containing-protein	gnl|CDD|272863	TIGR00028, Hypothetical_protein_Rv2872/MT2939/Mb2897., toxin-antitoxin system PIN domain toxin. Members of this protein consist almost entirely of a PIN (PilT N terminus) domain (see pfam01850). This family was originally defined a set of twelve closely related paralogs found in Mycobacterium tuberculosis, but additional members are found now Synechococcus sp. WH8102, etc. Inspection of genomic regions suggests these represent toxin components of toxin-antitoxin regions, potentially important to creating dormant persister cells.	4.13021e-20
NZ_CP040915.1|WP_139928589.1|2134925_2136401_-|leucyl-aminopeptidase	gnl|CDD|234863	PRK00913, PRK00913, multifunctional aminopeptidase A; Provisional.	0
NZ_CP040915.1|WP_139928614.1|2147691_2148087_-|VOC-family-protein	gnl|CDD|319924	cd07263, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	7.04613e-26
NZ_CP040915.1|WP_139928584.1|2132970_2134350_-|dihydrolipoyl-dehydrogenase	gnl|CDD|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP040915.1|WP_139928612.1|2146919_2147702_-|putative-protein-N(5)-glutamine-methyltransferase	gnl|CDD|274733	TIGR03704, PrmC_rel_meth, putative protein-(glutamine-N5) methyltransferase, unknown substrate-specific. This protein family is closely related to two different families of protein-(glutamine-N5) methyltransferase. The first is PrmB, which modifies ribosomal protein L3 in some bacteria. The second is PrmC (HemK), which modifies peptide chain release factors 1 and 2 in most bacteria and also in eukaryotes. The glutamine side chain-binding motif NPPY shared by PrmB and PrmC is N[VAT]PY in this family. The protein substrate is unknown. [Protein synthesis, Ribosomal proteins: synthesis and modification].	2.75818e-92
NZ_CP040915.1|WP_139931510.1|2148153_2148945_-|esterase-family-protein	gnl|CDD|223700	COG0627, COG0627, Predicted esterase [General function prediction only].	9.04746e-42

Protein sequences

>NZ_CP040915.1|WP_139928599.1|2139094_2139514_+|PIN-domain-containing-protein
MTRFLLDSNVLIAATIAEHEHHDAAATWLADAEGFAVCPVVEGALVRFLMRIGESGDTASRILAAVRSHPRSQFWPDAVSYVDVALSRIRGHRQVTDAYLARLASSKGSLLATFDTTLAELWPDQTMLIPHEKTHSPDV
>NZ_CP040915.1|WP_139928597.1|2138867_2139098_+|hypothetical-protein
MRTTVDLPPAVHQRARQLAAVQGKSLSAVIADLTIRGLAQLDTPLRLRVDERTGLPVLSVGRSVTDADVAEALEDA
>NZ_CP040915.1|WP_139928595.1|2138385_2138784_+|DUF2695-domain-containing-protein
MSVDDGVQVLEDELAGLAELLTAPRRGECLMCFTNRMLVEFGCDRTLRWARRYAQLRSPHAYALRRRLARHGAFCDCEIFANGWDVTVPTVRDPEHGAECWPSEVTGCRGVRTGSTQPCSLWALRRRETPLR
>NZ_CP040915.1|WP_139928593.1|2137370_2138270_+|hypothetical-protein
MPHARSLLSLLDLPRPEIERLWLASAGWKDQRSRRRARFADRRVATIFDGPAFRTRLAFDTAIDAVGAHRVDLPLVLGEREPIEDTAAILSSAVDAVVVRARDHQSVASLAAACDVPVINAMTDAGHPVEIFSEAFSVLERRGPIDDVVLTFVGDATNVLRSWCELTVGFELQVRHVCPPGHNLDEDFLAGLAELGQRGSVTTTHDLAEGVEGADVLYTDAWPLAARKPGRRRAAFEPYRITTDVLDAAGPKSILMHVMPVKRGDEVTAEAFADPRSVSLAAKRNLAPTHAAIVERALG
>NZ_CP040915.1|WP_139931507.1|2136904_2137300_+|hypothetical-protein
MGRVLILVYGIFAVAASARASVQLLRDAAEAPVAYSLSALAGAIYIVATIALAHNGRRMRRVAWVAVVIELLGVLIVGTLSLVEPALFPQDTVWSRYGGGYGFVPAVLPLLGIGWLWYSSPARVVARAERG
>NZ_CP040915.1|WP_139928591.1|2136446_2136800_+|hypothetical-protein
MQLTVTLTAILVALLGLWALWFAVMGRAVILRQLIAGGVVEVAIVAQLVVAFIGVARGYELADPWTFWGYVVTALFLLPVAGVWALADRTRWSSVVLVVACLAILAMQARVWQVWSA
>NZ_CP040915.1|WP_139928589.1|2134925_2136401_-|leucyl-aminopeptidase
MTDLNLSTKNPARISADALVLAVAQTDDGPRLFLPGQLPAKSVTRLAAVLPALGVTGKADEVVRVPAGDEVAATIVVLTGVGSVTREPTPEALRRAAGAATRSLAGTGDAVLALPAETAAQVGAVAEGALLGAYRFDHYKSTDPAPVARLELATPLARDKEAKAALARARAVGDGVRATRDLVNASPRHLYPETFADEARAAAKGTKVKVTVLDERELAAGGYGGILAVGQGSARPPRLVKLVYSPARPVAHYALVGKGITFDSGGLSLKPAKGMEAMKSDMAGAATVLHTVLAAAALELPVKVTGWLALAENMPGGGAQRPSDVITMRDGTTVEVLNTDAEGRLVLGDALVAACEEKPDAVLDIATLTGAQVVALGNRVAAVMGTEAMRDAVVATAGEVGEQVWPMPLPEELRESMKTPVADIANMGDRFGGMLVAGLFLREFVDETPWAHLDVAGPAFNESAPYGYTHKGGTGMGLRTLLGVLEAAARR
>NZ_CP040915.1|WP_139928587.1|2134553_2134871_+|oxidoreductase
MRLFSRRKRNDGLGTKEARARTLAHFREFTATRVGVEAYIEPPTAHDPHTMVLVARTGEWTRRRVPDVREARALAGELQIPIYDVHLTGYPASMRRWSAANRRRA
>NZ_CP040915.1|WP_139928584.1|2132970_2134350_-|dihydrolipoyl-dehydrogenase
MAETQEYDIVILGAGSGGYAAALRGAQLGMKVALIEGDKLGGTCLHRGCIPTKALLHSAEVADTIRESAAVGVQSTFGGIDMGGVNTFKDGIVARLYKGLQGLVSSRKVDLINGWGRLVAADTVEVDGTRYRGKNVVLASGSYSKSLPGLEIGGRVITSEQALQLDYVPKSAIVLGGGVIGVEFASVWNSFGADVTIIEGLPHLVPNEDESLSKGLERAFRKRKIAFHTKTMFAGVTQNDDGVVVTTQDGKTLEAELLLVAVGRGPATANLGYEENGIPMERGFVLTDDCLRTGVGNVYAVGDIVPGLQLAHRGFAQGIFVAEQIAGLNPAPIVESGIPRVTYCEPQVGSVGLTEAEAKETYGVDGVETVEYNLAGNGKSQILQTTGFIKLVREKDGPIVGVHMLGDRVGELIGEGQLMVNWEAYPEDVASLVHAHPTQNEAVGEAALALAGKPLHAHN
>NZ_CP040915.1|WP_139928582.1|2131146_2132946_-|2-oxoglutarate-dehydrogenase,-E2-component,-dihydrolipoamide-succinyltransferase
MSESVKMPALGESVTEGTVTRWLKAVGESVEVDEPLLEVSTDKVDTEVPSPVAGVVEKILVEEDETVEVGAELVVIGDGTGGGESAPAEDSAPAETSPAASEAPAAEEVEAAQPVSAEAAPAEEAKAQATQNAPTGGSAPAGEAVKMPALGESVTEGTVTRWLKAEGETVEVDEPLLEVSTDKVDTEVPSPVAGTVLKILVQEDETVEVGADLVIVGQAGAAAPAAEAPKEAPAEAPAPEAPKAEAPKAEAPKAEAPKAEAPKAEAPKAEAPKTAQPARAEAAPAAAGTAYITPLVRKLAVEKGIDLSSLTGTGVGGRIRKQDVEAAAEKAAAEKAAAQAAPAAAPAGAPAKQPTQVEVSPLRGTTEKMSRLRKVIAKRMRESLDTSTQLTSVMEVDVTRVATLRARAKNAFQTAEGTKLTFLPFFVKAATEALKSHPKLNATIDGDNVIYHGAEHMGIAVDTPRGLLVPVIKDAGDLTIGGIAKKINDLAARTRDSKVTPDELSGSTFTITNTGSAGLLIDTPIINQPEVAIMGVGTIVKRPAVVKDAEGNETIGIRSIIYLSLTYDHRLVDGADAGRFLQTVKARLEEGAFEAEVGL
>NZ_CP040915.1|WP_139928603.1|2140904_2141312_+|hypothetical-protein
MAKYLLLKHYRGAPSSVNDVPMDRWTPEEITAHVQYMNDFAARLESTGEYVDGQALSPEGTFVRYDGEGRPPVTDGPFAETKDLIAGWMVIDVESYDRAVELAGELSAAPGAGGKPIHEWLELRPFLAAPPTVTE
>NZ_CP040915.1|WP_139931508.1|2141317_2142457_+|RNA-polymerase-subunit-sigma-24
MDEALVRDLIPGVIGVLVRRGVSFAEAEDAVQDALVEALRAWPDDAPRDPKGWLVTVAWRKFLDGARADVARRNREVRAEHEAVPAVSPSVDDTLRLFFLCAHPSLTPASATALTLRAMGGLTTRQIARAYLVPEPTMAQRISRAKRTVSGERLDQPGDVATVLRVLYLVFNEGYSGDVDLAAEAIRLTRQLAGMIDHEEVSGLLALMLLHHARRPARTREDGRLVPLAEQDRTRWDTRLIAEGVDVLQRALARDRLGEFQAQAAIAALHADAQTADETDWVQIVEWYDELVRLTDSPVARLNRAVAVGEADGPRAGLAALAELDPALPRHTAVAAYLHERDGDMVAAARLYAEAARLAYNTAERDHLTLQAARLNAAR
>NZ_CP040915.1|WP_139931509.1|2142683_2145065_-|ATP-binding-cassette-domain-containing-protein
MATRTETQPSTPHVADSHDLIRVQGARENNLKDVSVEIPKRRLTVFTGVSGSGKSSLVFDTIAAESQRMINETYSAFVQGFMPNLPRPDVDLLDGLTTAIIVDQERMGANPRSTVGTATDANALLRILFSRLGQPQIGSPNAFSFNVPTVRASGAITVERGNKTKAEKATFTQLGGMCPRCEGMGSVNDFDLSALYDDSRSLNDGALTVPGYSMDGWYGRIFTGAGLPMDKPIGKFTKKELHTLLYAEPTKIKVEGINLTYEGLIPKIQKSMLSKDVDAMQPHVRAFVERAVTFTTCPDCDGTRLSPEARSSKIKGKNIADLCAMQISDLAAWVRELDEPSVAPLLTGLQHLLDSFTEIGLGYLSLDRPAGTLSGGEAQRTKMIRHLGSSLTDVTYVFDEPSIGLHPHDIERMNELLRQLRDKGNTVLVVEHKPEMIGIADHVVDLGPRAGTEGGEVVFEGSVEGLRASDTLTGRHLDDRATFKAGVRKPTGALEVRGAATHNLKDVDVDIPLGGMVVVTGVAGSGKSSLIHGSVAGRAGVVEIDQGAIRGSRRSNPATYTGLLDPIRKAFAKANGVKPALFSSNSEGACPTCNGAGVIYTELGVMATVESTCEECGGKRFQAAVLEYTLGGKNIAEVLAMPVTQAEEFFSDGDARIPAAHKILDRLADVGLGYLTLGQPLTTLSGGERQRLKLASQMGEKGEVYILDEPTTGLHLADVEQLLGLLDRLVDSGKSVIVIEHHQAVMAHADWIIDLGPGAGHDGGRIVFEGTPADLVAERSTLTGKHLAAYVGR
>NZ_CP040915.1|WP_139928605.1|2145246_2145657_-|VOC-family-protein
MDITIHYAFLPQTDPDAALAFYRDTLGFEVRNDVGYEDMRWITVGPPNQPATSIVLQPPAADPGITDDERRTILELIAKGSYAGVTLATDDLDGLFERLQARGADVVQEPTDQPYGVRDCAFRDPTGNLIRINQVG
>NZ_CP040915.1|WP_139928607.1|2145662_2146112_-|helix-turn-helix-domain-containing-protein
MTSTPAEAQRLRDLTLLRRVRDRMDREYAQPLDVEALARGVHMSAGHLSREFRRAYGESPYSYLMTRRIERAMALLRRGDLSVTEVCFAVGCSSLGTFSTRFTELVGVPPSVYRRQPSQVGKGIPPCLAKQVTRPVRNREARTREPQLA
>NZ_CP040915.1|WP_168205653.1|2146294_2146771_-|CHRD-domain-containing-protein
MRRKFAALASATAVLASSVLLSTSAVADERYGGHDNDREEKTLSAWLNGRNEVGHRGDRDGSGRAWFKVKLDGRDSEICYAISVRNLDRVTQAHIHKGERGENGPVVVPLKAPKDGFSKGCVDVRYRLARDILEDPHDYYANVHTKKYPDGAIRGQLR
>NZ_CP040915.1|WP_139928612.1|2146919_2147702_-|putative-protein-N(5)-glutamine-methyltransferase
MPADPALVARLRAAGSVFAEEEADLLAAAAASTAALTTLVRRRVAGEPLEQVLGWTAFYGLRVQVEPGVFVPRRRTELLAREAIAASQPGAVVVDLCCGSGAVALAVATHVPGIDLHAADVDGVAVRCARRNLGALGQVHQGDLFEALPAGLRGHVDVLVANGPYVPTDAIALMPPEARDHEPATALDGGPDGLAVLRQVVAGAALWLAPGGRLLLECADQQAAAIVAAVRDAGLGARLVHDDEHGAVVALGVAPDAARP
>NZ_CP040915.1|WP_139928614.1|2147691_2148087_-|VOC-family-protein
MPYVALVNVLVRDYDEAIAFYTGAFGLELLEDTPQGGTKRWVVVGSRTGGAGLRLALATKEAQLARVGTQSGDGVAFFLHVEDFDATVERALAHGAVATEEPRDEPHGRVIILEDLYGNRWDVIEPAGDAG
>NZ_CP040915.1|WP_139931510.1|2148153_2148945_-|esterase-family-protein
MALIRCDFFSEVLGLSTSMTVILPQATRAQIGMTGAAPAGPPPVLYLLHGLTDDATIWMRRTSIERYVADLGLAVVMPQVDRSFYVDERYGNRYGSFLTEELPELVGHFFRVSSRREDTFVAGLSMGGYGAMRWALTRPTRFAAAASLSGVLDLASQQGEDHRDDLYPRIFGDEPIAGGEFDLLALLHRAGAHDVHLPDLYVCCGTDDALFAGNETFRDEAARAGVPLTYDTGAGAHDWAYWDAKIRDVLAWLPVRAHDVKNQ
>NZ_CP040915.1|WP_139928616.1|2148994_2149600_-|biotin-transporter-BioY
MTVAAVPTSPRRVLADALPGAAAAGATVRARDLVLVLGGAAFVAAVGQAAIPLPFTPVPLTLGTFAVLLVGAALGPARGALSIAVLVLGGVAGIPVFADGNSGWAFASFGYVLGYLPAAACLGWLARRGGDRSTWRTGAAAVAATALVYAVGLPWLMAHLGVGLAEGLALGVTPFLIGDVVKAVAAALLLPGTWRLLGERR

Crispr_ID: NZ_CP040915_10

• CRISPR_ID: NZ_CP040915_10
• CRISPR_location: 3813603-3813815
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP040915_10

Consensus_repeat	Method
CGGCCGCTACGACGAGGGCGAGGTGGCCGAGGA	CRISPRCasFinder

spacers of NZ_CP040915_10

>10.1|3813636|27|NZ_CP040915|CRISPRCasFinder
ACGCCTCGTCGAGGACGAGCACACCCG
>10.2|3813696|27|NZ_CP040915|CRISPRCasFinder
GGTGATCGCCAAGGAGGAAGGCGTCCA
>10.3|3813756|27|NZ_CP040915|CRISPRCasFinder
CACCCTCGACGCCGAGGAGGGCATCGA

CRISPR arrays and Neighbor proteins around NZ_CP040915_10

CRISPR arrays

The CRISPR arrays of NZ_CP040915_10

>merge|NZ_CP040915|10|3813603-3813815|CRISPRCasFinder
CGGCCGCTACGACGAGGGCGAGGTGGCCGAGGAACGCCTCGTCGAGGACGAGCACACCCGCGGCCGCTACGACGAGGGCGAGGTCGCCGAGGAGGTGATCGCCAAGGAGGAAGGCGTCCACGGTCGGTTCGACGAGGGCCAGGCGGCGGACGCCACCCTCGACGCCGAGGAGGGCATCGAGGGCAGCTTCGACGAGGGCCAGGCCAGCGACGA

>NZ_CP040915|10|10|3813603-3813815|CRISPRCasFinder
CGGCCGCTACGACGAGGGCGAGGTGGCCGAGGA	ACGCCTCGTCGAGGACGAGCACACCCG
CGGCCGCTACGACGAGGGCGAGGTCGCCGAGGA	GGTGATCGCCAAGGAGGAAGGCGTCCA
CGGTCGGTTCGACGAGGGCCAGGCGGCGGACGC	CACCCTCGACGCCGAGGAGGGCATCGA
GGGCAGCTTCGACGAGGGCCAGGCCAGCGACGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin	unknown	unknown	gnl|CDD|379416
NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP040915.1|WP_139930571.1|3813194_3813518_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176506
NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213191
NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|211705
NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein	unknown	unknown	gnl|CDD|380207
NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin	unknown	unknown	gnl|CDD|379416
NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|119324
NZ_CP040915.1|WP_139931682.1|3823255_3824026_+|3-oxoacid-CoA-transferase-subunit-A	unknown	unknown	gnl|CDD|224702
NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|119323
NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA	unknown	unknown	gnl|CDD|213364
NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|380551
NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB	unknown	unknown	gnl|CDD|274529
NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213186
NZ_CP040915.1|WP_139930556.1|3804655_3805258_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein	unknown	unknown	gnl|CDD|341286
NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase	unknown	unknown	gnl|CDD|223232

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin	gnl|CDD|379416	pfam14013, MT0933_antitox, MT0933-like antitoxin protein. This family of proteins contains the MT0933 protein, which has been identified as an antitoxin to /protein MT0934. This family of proteins is found in bacteria. Proteins in this family are typically between 61 and 90 amino acids in length.	0.000550003
NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.60781e-16
NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase	gnl|CDD|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	2.97177e-62
NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA	gnl|CDD|213364	cd12830, MtCorA-like, Mycobacterium tuberculosis CorA-like subfamily. This bacterial subfamily belongs to the Thermotoga maritima CorA (TmCorA)-like family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subfamily includes the Mg2+ transporter Mycobacterium tuberculosis CorA (which also transports Co2+). Thermotoga maritima CorA forms funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport by a related protein, Saccharomyces cerevisiae Alr1p. Natural variants in this signature sequence may be associated with the transport of different divalent cations. The functional diversity of the MIT superfamily may also be due to minor structural differences regulating gating, substrate selection, and transport.	2.15027e-146
NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|211705	TIGR01963, D-beta-hydroxybutyrate_dehydrogenase, 3-hydroxybutyrate dehydrogenase. This model represents a subfamily of the short chain dehydrogenases. Characterized members so far as 3-hydroxybutyrate dehydrogenases and are found in species that accumulate ester polmers called polyhydroxyalkanoic acids (PHAs) under certain conditions. Several members of the family are from species not known to accumulate PHAs, including Oceanobacillus iheyensis and Bacillus subtilis. However, polymer formation is not required for there be a role for 3-hydroxybutyrate dehydrogenase; it may be members of this family have the same function in those species.	6.96144e-97
NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein	gnl|CDD|380207	NF033206, ScyE_fam, ScyD/ScyE family protein. This family includes ScyE, a protein involved in scytomenin biosynthesis and export, and its paralog ScyD. Some members of the family contain a C-terminal PEP-CTERM domain that predictions anchoring to the outer membrane.	1.31926e-97
NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein	gnl|CDD|380551	cd06328, PBP1_SBP-like, periplasmic substrate-binding domain of active transport proteins (substrate binding proteins or SBPs). Periplasmic substrate-binding domain of active transport proteins found in gram-negative and gram-positive bacteria. Members of this group are initial receptors in the process of active transport across cellular membrane, but their substrate specificities are not known in detail. However, they closely resemble the group of AmiC and active transport systems for short-chain amides and urea (FmdDEF), and thus are likely to exhibit a ligand-binding mode similar to that of the amide sensor protein AmiC from Pseudomonas aeruginosa. Moreover, this binding domain has high sequence identity to the family of hydrophobic amino acid transporters (HAAT), and thus it may also be involved in transport of amino acids.	1.31925e-140
NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.83386e-20
NZ_CP040915.1|WP_139931682.1|3823255_3824026_+|3-oxoacid-CoA-transferase-subunit-A	gnl|CDD|224702	COG1788, AtoD, Acyl CoA:acetate/3-ketoacid CoA transferase, alpha subunit [Lipid metabolism].	9.04419e-98
NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|119323	cd06581, TM_PBP1_LivM_like, Transmembrane subunit (TM) of Escherichia coli LivM and related proteins. LivM is one of two TMs of the E. coli LIV-1/LS transporter, a Periplasmic Binding Protein (PBP)-dependent ATP-Binding Cassette (ABC) transporter involved in the uptake of branched-chain amino acids (AAs). These types of transporters generally bind type 1 PBPs. PBP-dependent ABC transporters consist of a PBP, two TMs, and two cytoplasmic ABCs, and are mainly involved in importing solutes from the environment. The solute is captured by the PBP, which delivers it to a gated translocation pathway formed by the two TMs. The two ABCs bind and hydrolyze ATP and drive the transport reaction. E. coli LivM forms a heterodimer with another TM, LivH, to generate the transmembrane pore. LivH is not included in this subgroup. The LIV-1/LS transporter is comprised of two TMs (LivM and LivH), two ABCs (LivG and LivF), and one of two alternative PBPs, LivJ (LIV-BP) or LivK (LS-BP). In addition to transporting branched-chain AAs including leucine, isoleucine and valine, the E. coli LIV-1/LS transporter is involved in the uptake of the aromatic AA, phenylalanine.	3.00577e-58
NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213191	cd03224, ABC_TM1139_LivF_branched, ATP-binding cassette domain of branched-chain amino acid transporter. LivF (TM1139) is part of the LIV-I bacterial ABC-type two-component transport system that imports neutral, branched-chain amino acids. The E. coli branched-chain amino acid transporter comprises a heterodimer of ABC transporters (LivF and LivG), a heterodimer of six-helix TM domains (LivM and LivH), and one of two alternative soluble periplasmic substrate binding proteins (LivK or LivJ). ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules.	3.22381e-87
NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin	gnl|CDD|379416	pfam14013, MT0933_antitox, MT0933-like antitoxin protein. This family of proteins contains the MT0933 protein, which has been identified as an antitoxin to /protein MT0934. This family of proteins is found in bacteria. Proteins in this family are typically between 61 and 90 amino acids in length.	2.90272e-05
NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB	gnl|CDD|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase	gnl|CDD|223232	COG0154, GatA, Asp-tRNAAsn/Glu-tRNAGln amidotransferase A subunit and related amidases [Translation, ribosomal structure and biogenesis].	8.23732e-118
NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|119324	cd06582, TM_PBP1_LivH_like, Transmembrane subunit (TM) of Escherichia coli LivH and related proteins. LivH is one of two TMs of the E. coli LIV-1/LS transporter, a Periplasmic Binding Protein (PBP)-dependent ATP-Binding Cassette (ABC) transporter involved in the uptake of branched-chain amino acids (AAs). These types of transporters generally bind type 1 PBPs. PBP-dependent ABC transporters consist of a PBP, two TMs, and two cytoplasmic ABCs, and are mainly involved in importing solutes from the environment. The solute is captured by the PBP, which delivers it to a gated translocation pathway formed by the two TMs. The two ABCs bind and hydrolyze ATP and drive the transport reaction. E. coli LivH forms a heterodimer with another TM, LivM, to generate the transmembrane pore. LivM is not included in this subgroup. The LIV-1/LS transporter is comprised of two TMs (LivM and LivH), two ABCs (LivG and LivF), and one of two alternative PBPs, LivJ (LIV-BP) or LivK (LS-BP). In addition to transporting branched-chain AAs including leucine, isoleucine and valine, the E. coli LIV-1/LS transporter is involved in the uptake of the aromatic AA, phenylalanine.	7.32702e-58
NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein	gnl|CDD|341286	cd17631, FACL_FadD13-like, fatty acyl-CoA synthetase, including FadD13. This family contains fatty acyl-CoA synthetases, including Mycobacterium tuberculosis acid-induced operon MymA encoding the fatty acyl-CoA synthetase FadD13 which is essential for virulence and intracellular growth of the pathogen. The fatty acyl-CoA synthetase activates lipids before entering into the metabolic pathways and is also involved in transmembrane lipid transport. However, unlike soluble fatty acyl-CoA synthetases, but like the mammalian integral-membrane very-long-chain acyl-CoA synthetases, FadD13 accepts lipid substrates up to the maximum length of C26, and this is facilitated by an extensive hydrophobic tunnel from the active site to a positively charged patch. Also included is feruloyl-CoA synthetase (Fcs) in Rhodococcus strains where it is involved in biotechnological vanillin production from eugenol and ferulic acid via a non-beta-oxidative pathway.	1.4156e-170
NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase	gnl|CDD|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	9.75475e-26
NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213186	cd03219, ABC_Mj1267_LivG_branched, ATP-binding cassette component of branched chain amino acids transport system. The Mj1267/LivG ABC transporter subfamily is involved in the transport of the hydrophobic amino acids leucine, isoleucine and valine. MJ1267 is a branched-chain amino acid transporter with 29% similarity to both the LivF and LivG components of the E. coli branched-chain amino acid transporter. MJ1267 contains an insertion from residues 114 to 123 characteristic of LivG (Leucine-Isoleucine-Valine) homologs. The branched-chain amino acid transporter from E. coli comprises a heterodimer of ABCs (LivF and LivG), a heterodimer of six-helix TM domains (LivM and LivH), and one of two alternative soluble periplasmic substrate binding proteins (LivK or LivJ).	4.12057e-104

Protein sequences

>NZ_CP040915.1|WP_139930571.1|3813194_3813518_+|hypothetical-protein
MTRKHDPDAEEPRAAPPGRGRYDEGQASDEDLQAELGRHHGRYDDGERTDTTHPSTDELLRGRYDEGQATDADLAAGVRRPHGRYDEGTRAPDADSDDAGDESRSDF
>NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin
MSIGDLGDKAKDLAGSEKAEGISDSGIEKAKDAASEKTGGKFDEQLDKGGDAADQRLGNE
>NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase
MTQIHELSALDLAAAVRAGEVSPSEIADHTLERARRLGPQVGAFVHLAEKRAHAQAAEAEEQLSAVGTAARDDGVLPPFLGVPAPVKDLTMVAGLPFECGSAAFAGNVASVDDGVVTLLRAAGTLMVGKTTTPELGLPPYTEPDVAPPARTPWDLTRSAGGSSGGAAAAVAAGIVPVAHGSDGGGSIRIPAAATGLVGLKPSRGRISSGPYGVDGAGLGVNGVLTRTVRDTAAFLDVLAPPWPGDHYLLPGPRSTFLQACDQPPAPLRVGVLTEPVNVAGAPVHPGARAAVDRAARLLEGLGHHLAEAPVPFAPEQWDAFMPLWAVGVLGAPVPPEQEELLVPLTRWMRELGRRFTGAQYAQAVTDVQRLTRQTALAWSAFDVILTPTLAQPPALIGALRDDSDPAGDFAAQKAFTPWTSAWNLIGAPAISLPLHRQVVDEGDGARELPFGVMLGARLGQEETLLALAAQLEAADPWPMFAPGVEV
>NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin
MGFDDLARKAKDAFQSEKVQQALRSEKAETVSDTVLEKAAGMADKATGGKYEQQIAGARNMADTKIGTDNPSSLPDPRRRERAGGDPRPPVTAGTGQEGRR
>NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA
MTVVDNVIYVDGARAASPPTLEATFGLLREHGGMAWLGLYRPDAAEVRAVAQEFDLHELAEEDTNKAHQRPKLERYGHTLFTVLRPARYVDSTEKVEFGELHVFTGPSFVVTVRHAESPDLGEVRRRLEREPHMLRLGPEAVLYAILDQVVDEYAPVAAGLENDIDEIEDELFSSDPTVSRRIYELSREVIAFQRATHPLLPILENLEQGFDRYGVDIELQHKLRDVHDHALRIVERADSFRALLQNALLVNATLVAQQQNDETRRLTEASYLQSEQVKRISSWAAILFAPTLIGTIYGMNFRHMPELAWVLGYPLALLGMVVMGTVLYLVFKRHRWL
>NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB
MDTKLTTKSQEAIAEAIRAASTAGNPQLEPAHVLAALLQQEGGVAAALLDAVGADRGAIAQRVRASLATLPGASGSSVAQPQTSRATMTMITDAGNEARALGDEYVSTEHLLVALAASTSPAGEILRAAGANREGLLAALPTVRGTGKVTSPDPEGTFKALEKYGQDMTAAARDGKLDPVIGRDAEIRRVVQVLSRRTKNNPVLIGEPGVGKTAVVEGLAQRIVAGDVPDSLRGKRLIALDLAAMVAGAKYRGEFEERLKAVLEEIKSSDGEVVTFIDELHTVVGAGASEGSMDAGNMLKPMLARGELRLVGATTLDEYRERIEKDPALERRFQQVFVGEPSVEDTVAILRGIAPRYEAHHKVRISDGALVAAAALSHRYITGRQLPDKAIDLVDEAASRLRMELDSSPIEIDELRRTVDRLKMEELALAKSDDPASQERLEKLRADLADRQEELASMTARWEAEKAGHNRVGDIKAQLDALRTESDRAQREGDLETASRLLYGEIPTLERELAAAEQAEEAGAVEGAATRQAPMVTDHVGPDEVAEVVATWTGIPVGRLLQGETEKLLHMEDVIGQRLIGQRTAVRAVSDAVRRSRAGVADPDRPTGSFLFLGPTGVGKTELAKSLADFLFDDERATVRIDMSEYSEKHSVARLVGAPPGYVGYEEGGQLTEAVRRRPYAVVLLDEVEKAHPEVFDILLQVLDDGRLTDGQGRTVDFRNTILVLTSNLGSQFLVDQSLDEAAKREAVMAAVRVSFKPEFLNRLDDVVIFDALSLDELGSIVDLQVDRLALRLAERRLRLEVTDAAREWLALEGYDPAYGARPLRRLIQREIGDTLAKMLLAGEVHDGDTVTVDRADIDPAAALAQTGSLPEGQGLVLTVATPEGAVRT
>NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase
MTTFEALRDLDFPVGVVVTDADGVVATYGETGTVFRWASVTKLVSALATLVAVKRGLVGLDDPAGPEGATVRHLLAHASGVPFDAGATISPVGRRRVYSNYGIELVAEHVSEQVGADFTSWAEETVIDPLGMSTVLIEGSPAHAASGSAEDLARLGRELLAPTLLDDELFAEATQVVFPGLSGVLPGFGRQEHNDWGLGFEIRDHKSPHWTGASSSPRTFGHFGQSGSFLWVDPDAQLAAAFLGAKPFGEWAGRTWPRLTDAILADHARA
>NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase
MTTTDLDPRPDGQPATTGLPLVIAHRGNSSVAPENTLAALESAWRVGADVIEIDLQLTADGVAVVIHDETVDRTTNGAGRVDRLTAAQVADLDAGDWFSDHFGGQRVPTGEDLLAFFVAHPPICLLAEFKGPWGTEEVRQVTDAVDLMGLADRMVVQSFDVATVEALRAAAPELPRGLLVDELPEDLLALCRELRVMTLNPSGRLLRREPDLVDALHGEGLRTMVWTLDEPAHWAAAVAAGVDGIITDRPDRLRGWLAAR
>NZ_CP040915.1|WP_139930556.1|3804655_3805258_-|hypothetical-protein
MTTLPVHHVPQFFVRQHLTMMVNRYEVLAANPDGAEGPLLAFAEQKRMAMKEHVTFYTDRDKQRPVFSFKARKVIDPSSGYDVWDAAGQPIGFFRKDFKASLVRSTWHVSGSGLEARGTERNRGVAVLRRVWDFIPVLGETWVPFLFHFDFTDNATGQTVMSSQKHVAVRDRYTITVPDPRLDFRLAVSIAVALDALQSR
>NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein
MRRTRLSLAAAGAACAVVALGAAPALGHGGGSEENPEVVVSGLDGPRGLALGWHGDLYVAQAGRGGDGPCIAGPEGPTCLGDTGKISRVDVRRGKVHDVVTGLPSLAAEDGSAAIGPSDVAFDRHGKLHATVGLGNNPELLADLLADGADEDLVEQLASVNRVRHGELHEYADIADFELDKNPEDSDLDTNPHSLTFTRKLTVVADAGGNSLLGVRPDGKIVTLATFPQEAEVDNPLAPGTKIAPDPVPNAVVKGPDGALYVGQLTGFPFVTGTATVWRIVPGEKPTVYADGFTNVIDLAFTEDGNLLVLEIAQNGLASDDTTGALFEVNRKHTDDHKLLTDDLTLPGGLAVHKDTVYISNQTIVPGQGEILRFELD
>NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein
MRATRKSLALTLGVATMLAVAACAPSTGGGGNESTSGSSESTTEAAEGGGEPINIGIITSTTGPLAAYGETFVDGFEAGLDYATDGTGEVNGSPLEVKFEDDGGDTDRAVTLARDLIGQGYTILGGTASSGIALSLAEQAEQNKVLYVSGPAASDAITGINDYTFRSGRQSLQDVATAGSFVDVEGQQVLVLAQDNAFGQGNFAAVQAVLGAKGAEVTSVMVPEDVTEFTPFAAQVRDAAPTMVFVAWAGATSGAMWQALDQQGVLDDITVVTGLGDASTFGAYGAASDKIDFLNHYFPGAPDNEINAAMVEHVEAAGGTPDLFTPDGFTAAQMIVRAIEEAGGADDVDAMIAALEGWSFDGPKGSYTIRASDHALIQPMFQVKLVSDGNGGWTPELVSEAAAEDVAPPEAG
>NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein
MPSSAALTVESLSFQVGGAKILTDVNLEVAPGEMIGVIGPNGAGKTTLFNMISGIHAPTAGRVLLGGTEITHEPIHRRAKAGLGRTFQTSNLFPGLSVAENVRLAAQRHLGGNLSVWRFPRRGDHASTLAAGYLDEVGLTDLAEAPASGLSHGDKRKLEIAVLLAMDPKVILLDEPMAGVARADVPGLSEVIRRMHRDHKCTVLMVEHHIDVVLGLVERVAVLHQGTILALDQPDAIMADPLVQSAYLGAPV
>NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein
MSPILEVEHLSATIAGQPVIEDITFSVPATGVTAVLGRNGVGKTSTMKAVMGLIARSGKVVFDGVRIDREDTHRIVRRGIGYVPEDREVFGSLTVAENLRLAERDAHPRRDLVEQLFPDLVRRGGQRAGTLSGGQQQMLSLARALLNDNRLLLVDEPTKGLAPKIVTEVAEALEEAARTVPVLLVEQNLPVIERLAADVVVIDSGRVVHTGQAGALLADAEAVHRLLGVHADTADSVAADAVAAATAPEGVK
>NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease
MSTIVLLLITGLGLGALYFLVASGLSLIYGLMGVLNFAHGSFLTLGAFAGWEVARRIGPGTWTGFLVALLVGALAGALIAALTELLLIRPLYNRHIEQVLVTVGLGLATVALFEGIWGTDAINISGPEWLSGTTTILGARVPNDRFLAIAVAVLVLAALVAFLKFTRFGLIIRAGVENRAMVTALGIDVRRSFTLVFAIGGAAAGLGGVLASQYFDYVSAHLGATLLIFAFIVTVIGGLGSLGGAAAAAVLVAIPQQFANYYWGVGDLIAVLALAVVLLLRPSGLMGAKA
>NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease
MTTSTHAPERTDASTPEPRRARGGQVSRRGLTPWLVGIGVAVVMFCLPLLNLSLPGVLPGPTYTPGSLHLLALCLLFAALALSYHLLYGVAGMLSFGHALYFAAGAYGLAILLDRTELGLLTAGALVLVGAIVLANVVGAISLRVSGVSFAMVTLAFAQAGNVLARRNTAGLTGGEEGVGLRTTNVPDALIGVVNTRTIYWVALAVLLVVYVVVTWVQRSRAGHVVEATRENEMRVRVIGQQPYLIRLLTFVIAGALAALIGMAYLVLQSQAVPQISSADFTITVLVMVVLGGVGSRWGAIVGAVVYTLLDQRLGVFASSAFVDSLPAVLRVPLGEPLFILGVLFILVVLFMPGGIAGAVDRLRRGGSGRSGTGRGGAGHGGRRRVGKGRRAAGSHSETAAESTERQRLEELA
>NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein
MSDNRHTIGRWTADRARLSPDAVAIEERGHATTYARLDTRATALAERLVRAGYGRGDRVATLTRNSTDHVVLFFACAKAGLVLVPLSWRLSTDELGYQLRHARPALVLVQATLADSARAALAGLDPAPAVELLGADGVEQHVPYPVRTDPAPPGPQRPVADDDPLLIVYTSGTASAPKGAILTHANCFWTNLSLSGAIGLTEHDVVLAVLPQFHVGGWNIQPLLAWWTGATVVLEPEFDAGRALAAIAAHGVTTTMGVPTIYRLLAEHPTFADADLSSLTHAVVGGATMPPALLRTWHDRGVRVTQGYGLTEAGPNVLALPASDAAAHLGSVGKPYPHVEVTVTDPATGQVLPGSGRGELLVRGPNVFAGYFRDPEATAETLRDGWLHTGDLVERDAEGFFRVVDRIKDIYISGGENIAPAEVEAALTAHPEVLEAAVVGVLDQRWGEVGHAYVVRAAGSRLTSEQVIAHTRTLLAAFKAPRTVDFVDQLPRTALHKVRRGALPRPAPTAGRAGEPPAGQPGAGHPVVGRPATGQPAAALRLVSGDEGAAR
>NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator
MSALPRTERGGRTRAKILEVATAVFAERGYHDASIVKITEAAGVGQGTFYLYFASKQEVFEEVVRDLNSRVRRAMFEASNGQAGRLAAEREGFRAYFRFTADNPALYRIMRQAEFVAPHVLREHYERIAAGYVAGLQDAQQHGELAESIEPEVAAWALMGIGELVGLRWVLWEHENGNGHATMPPHVFESTMRLIERALTPLPGEGSTTEGRSS
>NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase
MSSTSLAGRRAVVTGGGAGIGAACARALAAEGAHVVVADRDEAAATAVANEVNGEAWVVDLDNTRALDGLALEADVLVNNAGIQVVRPIEEFDPEDFRRIQRLMIEAPFLLVRAALPHMYARGWGRVVNLSSVHGLIASPFKVAYVTAKHALEGLSKVTALEGAAHGVTSNCVNPAYVRTALVEKQIADQARVHGISEAEVVEKVLLTEQSVKRLVEPEEVASLVVWLTGPHAGMATGGSYTLDGGWHAR
>NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase
MSIDSAPRTHTYTELDVAVDGGMLHAGVWEPRGAHDESRAATDGEPGAPSDGVPTVLAIHGITATHRAWDWVAPALAGTRVVAPDLRGRGRSNTLTGPFGMARHADDVAALARDVGARQVVVAGHSMGAFVAVVLAHRHPDLVRSLVLVDGGLPLALPAGLDADAAMTAVLGPAAERLAMSFPDHAAYREFWRSHPAFATCWAEDLGGYFDYDLEPVDGVFRASARLEAMTGDQRELFTGESLLPALSALAVPTTFLRAPFGLMADNPLYQPGTVEEWRGRLPTLRSVEVPDVNHYTIVMTPPGAATVVREITRHLAASTP
>NZ_CP040915.1|WP_139931682.1|3823255_3824026_+|3-oxoacid-CoA-transferase-subunit-A
MDKVVGSAAEAVADIGDGASLAVGGFGLSGNPIALIEALLAQGASGLEVVSNNCGVDDWGLGILLGAGRLAKMTASYVGENKEFERQFLSGELEVELTPQGTLAEKLRAGGSGIAAFFTPTGVGTQVAEGGLPRRYDGAGQVAVASPVKEVRMFDFAGGSREFVLEEAITTDFALVHAIRGDRHGNLVFNKAARNFSPLAAMAGRVCIAQVEELVEPGELDPDEVHLPGIYVHRLVEVGGGIEKRIEKRTVREGSN

Crispr_ID: NZ_CP040915_9

• CRISPR_ID: NZ_CP040915_9
• CRISPR_location: 3813248-3813473
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP040915_9

Consensus_repeat	Method
CCGCGGCCGGTACGACGAGGGCCAGGCCACGGACGAGG	PILER-CR
CGGCCGCTACGACGAGGGCGAGGTGGCCGAGGA	CRISPRCasFinder

spacers of NZ_CP040915_9

>9.1|3813286|25|NZ_CP040915|PILER-CR
ATCTGCAGGCCGAGCTCGGCCGGCA
>9.2|3813349|41|NZ_CP040915|PILER-CR
GAGCGGACCGACACCACGCATCCCTCCACCGACGAGCTGCT
>9.3|3813284|30|NZ_CP040915|CRISPRCasFinder
GGATCTGCAGGCCGAGCTCGGCCGGCACCA
>9.4|3813347|30|NZ_CP040915|CRISPRCasFinder
CACGCATCCCTCCACCGACGAGCTGCTCCG
>9.5|3813410|30|NZ_CP040915|CRISPRCasFinder
GGACCTCGCGGCCGGAGTCCGGCGCCCGCA

CRISPR arrays and Neighbor proteins around NZ_CP040915_9

CRISPR arrays

The CRISPR arrays of NZ_CP040915_9

>merge|NZ_CP040915|9|3813248-3813473|PILER-CR,CRISPRCasFinder
GCGCGGCCGTTACGACGAGGGCCAGGCCTCGGACGAGGATCTGCAGGCCGAGCTCGGCCGGCACCACGGCCGGTACGACGACGGCGAGCGGACCGACACCACGCATCCCTCCACCGACGAGCTGCTCCGCGGCCGGTACGACGAGGGCCAGGCCACGGACGCGGACCTCGCGGCCGGAGTCCGGCGCCCGCACGGCCGGTACGACGAGGGGACGCGAGCCCCCGAC

>NZ_CP040915|9|1|3813248-3813411|PILER-CR
GCGCGGCCGTTACGACGAGGGCCAGGCCTCGGACGAGG	ATCTGCAGGCCGAGCTCGGCCGGCA
CCACGGCCGGTACGACGACGGCGAGCGGACCGACACCA	CGCATCCCTCCACCGACGAGCTGCTCCGCGGCCGGTACGAC
GAGGGCCAGGCCACGGACGCGG

>NZ_CP040915|9|9|3813251-3813473|CRISPRCasFinder
CGGCCGTTACGACGAGGGCCAGGCCTCGGACGA	GGATCTGCAGGCCGAGCTCGGCCGGCACCA
CGGCCGGTACGACGACGGCGAGCGGACCGACAC	CACGCATCCCTCCACCGACGAGCTGCTCCG
CGGCCGGTACGACGAGGGCCAGGCCACGGACGC	GGACCTCGCGGCCGGAGTCCGGCGCCCGCA
CGGCCGGTACGACGAGGGGACGCGAGCCCCCGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin	unknown	unknown	gnl|CDD|379416
NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP040915.1|WP_139930573.1|3813540_3813837_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176506
NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213191
NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|211705
NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein	unknown	unknown	gnl|CDD|380207
NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|380551
NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|119324
NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|119323
NZ_CP040915.1|WP_139930552.1|3802490_3803273_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197320
NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA	unknown	unknown	gnl|CDD|213364
NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin	unknown	unknown	gnl|CDD|379416
NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB	unknown	unknown	gnl|CDD|274529
NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213186
NZ_CP040915.1|WP_139930556.1|3804655_3805258_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein	unknown	unknown	gnl|CDD|341286
NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase	unknown	unknown	gnl|CDD|223232

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin	gnl|CDD|379416	pfam14013, MT0933_antitox, MT0933-like antitoxin protein. This family of proteins contains the MT0933 protein, which has been identified as an antitoxin to /protein MT0934. This family of proteins is found in bacteria. Proteins in this family are typically between 61 and 90 amino acids in length.	0.000550003
NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.60781e-16
NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase	gnl|CDD|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	2.97177e-62
NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213191	cd03224, ABC_TM1139_LivF_branched, ATP-binding cassette domain of branched-chain amino acid transporter. LivF (TM1139) is part of the LIV-I bacterial ABC-type two-component transport system that imports neutral, branched-chain amino acids. The E. coli branched-chain amino acid transporter comprises a heterodimer of ABC transporters (LivF and LivG), a heterodimer of six-helix TM domains (LivM and LivH), and one of two alternative soluble periplasmic substrate binding proteins (LivK or LivJ). ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules.	3.22381e-87
NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|211705	TIGR01963, D-beta-hydroxybutyrate_dehydrogenase, 3-hydroxybutyrate dehydrogenase. This model represents a subfamily of the short chain dehydrogenases. Characterized members so far as 3-hydroxybutyrate dehydrogenases and are found in species that accumulate ester polmers called polyhydroxyalkanoic acids (PHAs) under certain conditions. Several members of the family are from species not known to accumulate PHAs, including Oceanobacillus iheyensis and Bacillus subtilis. However, polymer formation is not required for there be a role for 3-hydroxybutyrate dehydrogenase; it may be members of this family have the same function in those species.	6.96144e-97
NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein	gnl|CDD|380207	NF033206, ScyE_fam, ScyD/ScyE family protein. This family includes ScyE, a protein involved in scytomenin biosynthesis and export, and its paralog ScyD. Some members of the family contain a C-terminal PEP-CTERM domain that predictions anchoring to the outer membrane.	1.31926e-97
NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein	gnl|CDD|380551	cd06328, PBP1_SBP-like, periplasmic substrate-binding domain of active transport proteins (substrate binding proteins or SBPs). Periplasmic substrate-binding domain of active transport proteins found in gram-negative and gram-positive bacteria. Members of this group are initial receptors in the process of active transport across cellular membrane, but their substrate specificities are not known in detail. However, they closely resemble the group of AmiC and active transport systems for short-chain amides and urea (FmdDEF), and thus are likely to exhibit a ligand-binding mode similar to that of the amide sensor protein AmiC from Pseudomonas aeruginosa. Moreover, this binding domain has high sequence identity to the family of hydrophobic amino acid transporters (HAAT), and thus it may also be involved in transport of amino acids.	1.31925e-140
NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.83386e-20
NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|119323	cd06581, TM_PBP1_LivM_like, Transmembrane subunit (TM) of Escherichia coli LivM and related proteins. LivM is one of two TMs of the E. coli LIV-1/LS transporter, a Periplasmic Binding Protein (PBP)-dependent ATP-Binding Cassette (ABC) transporter involved in the uptake of branched-chain amino acids (AAs). These types of transporters generally bind type 1 PBPs. PBP-dependent ABC transporters consist of a PBP, two TMs, and two cytoplasmic ABCs, and are mainly involved in importing solutes from the environment. The solute is captured by the PBP, which delivers it to a gated translocation pathway formed by the two TMs. The two ABCs bind and hydrolyze ATP and drive the transport reaction. E. coli LivM forms a heterodimer with another TM, LivH, to generate the transmembrane pore. LivH is not included in this subgroup. The LIV-1/LS transporter is comprised of two TMs (LivM and LivH), two ABCs (LivG and LivF), and one of two alternative PBPs, LivJ (LIV-BP) or LivK (LS-BP). In addition to transporting branched-chain AAs including leucine, isoleucine and valine, the E. coli LIV-1/LS transporter is involved in the uptake of the aromatic AA, phenylalanine.	3.00577e-58
NZ_CP040915.1|WP_139930552.1|3802490_3803273_+|exodeoxyribonuclease-III	gnl|CDD|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	5.50639e-116
NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA	gnl|CDD|213364	cd12830, MtCorA-like, Mycobacterium tuberculosis CorA-like subfamily. This bacterial subfamily belongs to the Thermotoga maritima CorA (TmCorA)-like family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subfamily includes the Mg2+ transporter Mycobacterium tuberculosis CorA (which also transports Co2+). Thermotoga maritima CorA forms funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport by a related protein, Saccharomyces cerevisiae Alr1p. Natural variants in this signature sequence may be associated with the transport of different divalent cations. The functional diversity of the MIT superfamily may also be due to minor structural differences regulating gating, substrate selection, and transport.	2.15027e-146
NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin	gnl|CDD|379416	pfam14013, MT0933_antitox, MT0933-like antitoxin protein. This family of proteins contains the MT0933 protein, which has been identified as an antitoxin to /protein MT0934. This family of proteins is found in bacteria. Proteins in this family are typically between 61 and 90 amino acids in length.	2.90272e-05
NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB	gnl|CDD|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase	gnl|CDD|223232	COG0154, GatA, Asp-tRNAAsn/Glu-tRNAGln amidotransferase A subunit and related amidases [Translation, ribosomal structure and biogenesis].	8.23732e-118
NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|119324	cd06582, TM_PBP1_LivH_like, Transmembrane subunit (TM) of Escherichia coli LivH and related proteins. LivH is one of two TMs of the E. coli LIV-1/LS transporter, a Periplasmic Binding Protein (PBP)-dependent ATP-Binding Cassette (ABC) transporter involved in the uptake of branched-chain amino acids (AAs). These types of transporters generally bind type 1 PBPs. PBP-dependent ABC transporters consist of a PBP, two TMs, and two cytoplasmic ABCs, and are mainly involved in importing solutes from the environment. The solute is captured by the PBP, which delivers it to a gated translocation pathway formed by the two TMs. The two ABCs bind and hydrolyze ATP and drive the transport reaction. E. coli LivH forms a heterodimer with another TM, LivM, to generate the transmembrane pore. LivM is not included in this subgroup. The LIV-1/LS transporter is comprised of two TMs (LivM and LivH), two ABCs (LivG and LivF), and one of two alternative PBPs, LivJ (LIV-BP) or LivK (LS-BP). In addition to transporting branched-chain AAs including leucine, isoleucine and valine, the E. coli LIV-1/LS transporter is involved in the uptake of the aromatic AA, phenylalanine.	7.32702e-58
NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein	gnl|CDD|341286	cd17631, FACL_FadD13-like, fatty acyl-CoA synthetase, including FadD13. This family contains fatty acyl-CoA synthetases, including Mycobacterium tuberculosis acid-induced operon MymA encoding the fatty acyl-CoA synthetase FadD13 which is essential for virulence and intracellular growth of the pathogen. The fatty acyl-CoA synthetase activates lipids before entering into the metabolic pathways and is also involved in transmembrane lipid transport. However, unlike soluble fatty acyl-CoA synthetases, but like the mammalian integral-membrane very-long-chain acyl-CoA synthetases, FadD13 accepts lipid substrates up to the maximum length of C26, and this is facilitated by an extensive hydrophobic tunnel from the active site to a positively charged patch. Also included is feruloyl-CoA synthetase (Fcs) in Rhodococcus strains where it is involved in biotechnological vanillin production from eugenol and ferulic acid via a non-beta-oxidative pathway.	1.4156e-170
NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase	gnl|CDD|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	9.75475e-26
NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213186	cd03219, ABC_Mj1267_LivG_branched, ATP-binding cassette component of branched chain amino acids transport system. The Mj1267/LivG ABC transporter subfamily is involved in the transport of the hydrophobic amino acids leucine, isoleucine and valine. MJ1267 is a branched-chain amino acid transporter with 29% similarity to both the LivF and LivG components of the E. coli branched-chain amino acid transporter. MJ1267 contains an insertion from residues 114 to 123 characteristic of LivG (Leucine-Isoleucine-Valine) homologs. The branched-chain amino acid transporter from E. coli comprises a heterodimer of ABCs (LivF and LivG), a heterodimer of six-helix TM domains (LivM and LivH), and one of two alternative soluble periplasmic substrate binding proteins (LivK or LivJ).	4.12057e-104

Protein sequences

>NZ_CP040915.1|WP_168205731.1|3812893_3813076_+|antitoxin
MSIGDLGDKAKDLAGSEKAEGISDSGIEKAKDAASEKTGGKFDEQLDKGGDAADQRLGNE
>NZ_CP040915.1|WP_139930569.1|3811322_3812783_-|amidase
MTQIHELSALDLAAAVRAGEVSPSEIADHTLERARRLGPQVGAFVHLAEKRAHAQAAEAEEQLSAVGTAARDDGVLPPFLGVPAPVKDLTMVAGLPFECGSAAFAGNVASVDDGVVTLLRAAGTLMVGKTTTPELGLPPYTEPDVAPPARTPWDLTRSAGGSSGGAAAAVAAGIVPVAHGSDGGGSIRIPAAATGLVGLKPSRGRISSGPYGVDGAGLGVNGVLTRTVRDTAAFLDVLAPPWPGDHYLLPGPRSTFLQACDQPPAPLRVGVLTEPVNVAGAPVHPGARAAVDRAARLLEGLGHHLAEAPVPFAPEQWDAFMPLWAVGVLGAPVPPEQEELLVPLTRWMRELGRRFTGAQYAQAVTDVQRLTRQTALAWSAFDVILTPTLAQPPALIGALRDDSDPAGDFAAQKAFTPWTSAWNLIGAPAISLPLHRQVVDEGDGARELPFGVMLGARLGQEETLLALAAQLEAADPWPMFAPGVEV
>NZ_CP040915.1|WP_139930567.1|3811020_3811326_+|antitoxin
MGFDDLARKAKDAFQSEKVQQALRSEKAETVSDTVLEKAAGMADKATGGKYEQQIAGARNMADTKIGTDNPSSLPDPRRRERAGGDPRPPVTAGTGQEGRR
>NZ_CP040915.1|WP_139930564.1|3809892_3810909_-|magnesium-and-cobalt-transport-protein-CorA
MTVVDNVIYVDGARAASPPTLEATFGLLREHGGMAWLGLYRPDAAEVRAVAQEFDLHELAEEDTNKAHQRPKLERYGHTLFTVLRPARYVDSTEKVEFGELHVFTGPSFVVTVRHAESPDLGEVRRRLEREPHMLRLGPEAVLYAILDQVVDEYAPVAAGLENDIDEIEDELFSSDPTVSRRIYELSREVIAFQRATHPLLPILENLEQGFDRYGVDIELQHKLRDVHDHALRIVERADSFRALLQNALLVNATLVAQQQNDETRRLTEASYLQSEQVKRISSWAAILFAPTLIGTIYGMNFRHMPELAWVLGYPLALLGMVVMGTVLYLVFKRHRWL
>NZ_CP040915.1|WP_139930562.1|3807144_3809814_-|ATP-dependent-chaperone-ClpB
MDTKLTTKSQEAIAEAIRAASTAGNPQLEPAHVLAALLQQEGGVAAALLDAVGADRGAIAQRVRASLATLPGASGSSVAQPQTSRATMTMITDAGNEARALGDEYVSTEHLLVALAASTSPAGEILRAAGANREGLLAALPTVRGTGKVTSPDPEGTFKALEKYGQDMTAAARDGKLDPVIGRDAEIRRVVQVLSRRTKNNPVLIGEPGVGKTAVVEGLAQRIVAGDVPDSLRGKRLIALDLAAMVAGAKYRGEFEERLKAVLEEIKSSDGEVVTFIDELHTVVGAGASEGSMDAGNMLKPMLARGELRLVGATTLDEYRERIEKDPALERRFQQVFVGEPSVEDTVAILRGIAPRYEAHHKVRISDGALVAAAALSHRYITGRQLPDKAIDLVDEAASRLRMELDSSPIEIDELRRTVDRLKMEELALAKSDDPASQERLEKLRADLADRQEELASMTARWEAEKAGHNRVGDIKAQLDALRTESDRAQREGDLETASRLLYGEIPTLERELAAAEQAEEAGAVEGAATRQAPMVTDHVGPDEVAEVVATWTGIPVGRLLQGETEKLLHMEDVIGQRLIGQRTAVRAVSDAVRRSRAGVADPDRPTGSFLFLGPTGVGKTELAKSLADFLFDDERATVRIDMSEYSEKHSVARLVGAPPGYVGYEEGGQLTEAVRRRPYAVVLLDEVEKAHPEVFDILLQVLDDGRLTDGQGRTVDFRNTILVLTSNLGSQFLVDQSLDEAAKREAVMAAVRVSFKPEFLNRLDDVVIFDALSLDELGSIVDLQVDRLALRLAERRLRLEVTDAAREWLALEGYDPAYGARPLRRLIQREIGDTLAKMLLAGEVHDGDTVTVDRADIDPAAALAQTGSLPEGQGLVLTVATPEGAVRT
>NZ_CP040915.1|WP_139930560.1|3806262_3807075_-|serine-hydrolase
MTTFEALRDLDFPVGVVVTDADGVVATYGETGTVFRWASVTKLVSALATLVAVKRGLVGLDDPAGPEGATVRHLLAHASGVPFDAGATISPVGRRRVYSNYGIELVAEHVSEQVGADFTSWAEETVIDPLGMSTVLIEGSPAHAASGSAEDLARLGRELLAPTLLDDELFAEATQVVFPGLSGVLPGFGRQEHNDWGLGFEIRDHKSPHWTGASSSPRTFGHFGQSGSFLWVDPDAQLAAAFLGAKPFGEWAGRTWPRLTDAILADHARA
>NZ_CP040915.1|WP_139930558.1|3805276_3806059_-|glycerophosphodiester-phosphodiesterase
MTTTDLDPRPDGQPATTGLPLVIAHRGNSSVAPENTLAALESAWRVGADVIEIDLQLTADGVAVVIHDETVDRTTNGAGRVDRLTAAQVADLDAGDWFSDHFGGQRVPTGEDLLAFFVAHPPICLLAEFKGPWGTEEVRQVTDAVDLMGLADRMVVQSFDVATVEALRAAAPELPRGLLVDELPEDLLALCRELRVMTLNPSGRLLRREPDLVDALHGEGLRTMVWTLDEPAHWAAAVAAGVDGIITDRPDRLRGWLAAR
>NZ_CP040915.1|WP_139930556.1|3804655_3805258_-|hypothetical-protein
MTTLPVHHVPQFFVRQHLTMMVNRYEVLAANPDGAEGPLLAFAEQKRMAMKEHVTFYTDRDKQRPVFSFKARKVIDPSSGYDVWDAAGQPIGFFRKDFKASLVRSTWHVSGSGLEARGTERNRGVAVLRRVWDFIPVLGETWVPFLFHFDFTDNATGQTVMSSQKHVAVRDRYTITVPDPRLDFRLAVSIAVALDALQSR
>NZ_CP040915.1|WP_139930554.1|3803337_3804471_-|ScyD/ScyE-family-protein
MRRTRLSLAAAGAACAVVALGAAPALGHGGGSEENPEVVVSGLDGPRGLALGWHGDLYVAQAGRGGDGPCIAGPEGPTCLGDTGKISRVDVRRGKVHDVVTGLPSLAAEDGSAAIGPSDVAFDRHGKLHATVGLGNNPELLADLLADGADEDLVEQLASVNRVRHGELHEYADIADFELDKNPEDSDLDTNPHSLTFTRKLTVVADAGGNSLLGVRPDGKIVTLATFPQEAEVDNPLAPGTKIAPDPVPNAVVKGPDGALYVGQLTGFPFVTGTATVWRIVPGEKPTVYADGFTNVIDLAFTEDGNLLVLEIAQNGLASDDTTGALFEVNRKHTDDHKLLTDDLTLPGGLAVHKDTVYISNQTIVPGQGEILRFELD
>NZ_CP040915.1|WP_139930552.1|3802490_3803273_+|exodeoxyribonuclease-III
MRLATWNVNSIRTRVDRVLAFLESSGTDVLAMQETKCRDDQFPALAFEAAGYEVAHHGLSQWNGVAVASRVGLEEIEIGFPGMPTWGEPAAAEARAIGVTCDGVRVWSLYVPNGRTLEDPHYRYKLEWLAALRAAAGGWLAADPDAEVALVGDWNIAPLDTDVWDMSVFEGATHVSEPERAAFRALEDAGFAEVTRTFVPQQYTYWDYQRLRFPRNEGMRIDFVHASPELAAHVVGATIHRDERKGKAPSDHVPVVIDID
>NZ_CP040915.1|WP_139930573.1|3813540_3813837_+|hypothetical-protein
MSEIQPQDPAQHVPGAPPEPHGRYDEGEVAEERLVEDEHTRGRYDEGEVAEEVIAKEEGVHGRFDEGQAADATLDAEEGIEGSFDEGQASDDTPSPTP
>NZ_CP040915.1|WP_139930575.1|3814068_3815307_+|ABC-transporter-substrate-binding-protein
MRATRKSLALTLGVATMLAVAACAPSTGGGGNESTSGSSESTTEAAEGGGEPINIGIITSTTGPLAAYGETFVDGFEAGLDYATDGTGEVNGSPLEVKFEDDGGDTDRAVTLARDLIGQGYTILGGTASSGIALSLAEQAEQNKVLYVSGPAASDAITGINDYTFRSGRQSLQDVATAGSFVDVEGQQVLVLAQDNAFGQGNFAAVQAVLGAKGAEVTSVMVPEDVTEFTPFAAQVRDAAPTMVFVAWAGATSGAMWQALDQQGVLDDITVVTGLGDASTFGAYGAASDKIDFLNHYFPGAPDNEINAAMVEHVEAAGGTPDLFTPDGFTAAQMIVRAIEEAGGADDVDAMIAALEGWSFDGPKGSYTIRASDHALIQPMFQVKLVSDGNGGWTPELVSEAAAEDVAPPEAG
>NZ_CP040915.1|WP_139930577.1|3815461_3816220_+|ATP-binding-cassette-domain-containing-protein
MPSSAALTVESLSFQVGGAKILTDVNLEVAPGEMIGVIGPNGAGKTTLFNMISGIHAPTAGRVLLGGTEITHEPIHRRAKAGLGRTFQTSNLFPGLSVAENVRLAAQRHLGGNLSVWRFPRRGDHASTLAAGYLDEVGLTDLAEAPASGLSHGDKRKLEIAVLLAMDPKVILLDEPMAGVARADVPGLSEVIRRMHRDHKCTVLMVEHHIDVVLGLVERVAVLHQGTILALDQPDAIMADPLVQSAYLGAPV
>NZ_CP040915.1|WP_139930579.1|3816216_3816975_+|ATP-binding-cassette-domain-containing-protein
MSPILEVEHLSATIAGQPVIEDITFSVPATGVTAVLGRNGVGKTSTMKAVMGLIARSGKVVFDGVRIDREDTHRIVRRGIGYVPEDREVFGSLTVAENLRLAERDAHPRRDLVEQLFPDLVRRGGQRAGTLSGGQQQMLSLARALLNDNRLLLVDEPTKGLAPKIVTEVAEALEEAARTVPVLLVEQNLPVIERLAADVVVIDSGRVVHTGQAGALLADAEAVHRLLGVHADTADSVAADAVAAATAPEGVK
>NZ_CP040915.1|WP_139930581.1|3816971_3817844_+|branched-chain-amino-acid-ABC-transporter-permease
MSTIVLLLITGLGLGALYFLVASGLSLIYGLMGVLNFAHGSFLTLGAFAGWEVARRIGPGTWTGFLVALLVGALAGALIAALTELLLIRPLYNRHIEQVLVTVGLGLATVALFEGIWGTDAINISGPEWLSGTTTILGARVPNDRFLAIAVAVLVLAALVAFLKFTRFGLIIRAGVENRAMVTALGIDVRRSFTLVFAIGGAAAGLGGVLASQYFDYVSAHLGATLLIFAFIVTVIGGLGSLGGAAAAAVLVAIPQQFANYYWGVGDLIAVLALAVVLLLRPSGLMGAKA
>NZ_CP040915.1|WP_139930583.1|3817840_3819082_+|branched-chain-amino-acid-ABC-transporter-permease
MTTSTHAPERTDASTPEPRRARGGQVSRRGLTPWLVGIGVAVVMFCLPLLNLSLPGVLPGPTYTPGSLHLLALCLLFAALALSYHLLYGVAGMLSFGHALYFAAGAYGLAILLDRTELGLLTAGALVLVGAIVLANVVGAISLRVSGVSFAMVTLAFAQAGNVLARRNTAGLTGGEEGVGLRTTNVPDALIGVVNTRTIYWVALAVLLVVYVVVTWVQRSRAGHVVEATRENEMRVRVIGQQPYLIRLLTFVIAGALAALIGMAYLVLQSQAVPQISSADFTITVLVMVVLGGVGSRWGAIVGAVVYTLLDQRLGVFASSAFVDSLPAVLRVPLGEPLFILGVLFILVVLFMPGGIAGAVDRLRRGGSGRSGTGRGGAGHGGRRRVGKGRRAAGSHSETAAESTERQRLEELA
>NZ_CP040915.1|WP_139930585.1|3819078_3820734_+|AMP-binding-protein
MSDNRHTIGRWTADRARLSPDAVAIEERGHATTYARLDTRATALAERLVRAGYGRGDRVATLTRNSTDHVVLFFACAKAGLVLVPLSWRLSTDELGYQLRHARPALVLVQATLADSARAALAGLDPAPAVELLGADGVEQHVPYPVRTDPAPPGPQRPVADDDPLLIVYTSGTASAPKGAILTHANCFWTNLSLSGAIGLTEHDVVLAVLPQFHVGGWNIQPLLAWWTGATVVLEPEFDAGRALAAIAAHGVTTTMGVPTIYRLLAEHPTFADADLSSLTHAVVGGATMPPALLRTWHDRGVRVTQGYGLTEAGPNVLALPASDAAAHLGSVGKPYPHVEVTVTDPATGQVLPGSGRGELLVRGPNVFAGYFRDPEATAETLRDGWLHTGDLVERDAEGFFRVVDRIKDIYISGGENIAPAEVEAALTAHPEVLEAAVVGVLDQRWGEVGHAYVVRAAGSRLTSEQVIAHTRTLLAAFKAPRTVDFVDQLPRTALHKVRRGALPRPAPTAGRAGEPPAGQPGAGHPVVGRPATGQPAAALRLVSGDEGAAR
>NZ_CP040915.1|WP_139930587.1|3820730_3821375_+|TetR-family-transcriptional-regulator
MSALPRTERGGRTRAKILEVATAVFAERGYHDASIVKITEAAGVGQGTFYLYFASKQEVFEEVVRDLNSRVRRAMFEASNGQAGRLAAEREGFRAYFRFTADNPALYRIMRQAEFVAPHVLREHYERIAAGYVAGLQDAQQHGELAESIEPEVAAWALMGIGELVGLRWVLWEHENGNGHATMPPHVFESTMRLIERALTPLPGEGSTTEGRSS
>NZ_CP040915.1|WP_139930589.1|3821371_3822124_+|SDR-family-NAD(P)-dependent-oxidoreductase
MSSTSLAGRRAVVTGGGAGIGAACARALAAEGAHVVVADRDEAAATAVANEVNGEAWVVDLDNTRALDGLALEADVLVNNAGIQVVRPIEEFDPEDFRRIQRLMIEAPFLLVRAALPHMYARGWGRVVNLSSVHGLIASPFKVAYVTAKHALEGLSKVTALEGAAHGVTSNCVNPAYVRTALVEKQIADQARVHGISEAEVVEKVLLTEQSVKRLVEPEEVASLVVWLTGPHAGMATGGSYTLDGGWHAR
>NZ_CP040915.1|WP_139930591.1|3822120_3823086_+|alpha/beta-fold-hydrolase
MSIDSAPRTHTYTELDVAVDGGMLHAGVWEPRGAHDESRAATDGEPGAPSDGVPTVLAIHGITATHRAWDWVAPALAGTRVVAPDLRGRGRSNTLTGPFGMARHADDVAALARDVGARQVVVAGHSMGAFVAVVLAHRHPDLVRSLVLVDGGLPLALPAGLDADAAMTAVLGPAAERLAMSFPDHAAYREFWRSHPAFATCWAEDLGGYFDYDLEPVDGVFRASARLEAMTGDQRELFTGESLLPALSALAVPTTFLRAPFGLMADNPLYQPGTVEEWRGRLPTLRSVEVPDVNHYTIVMTPPGAATVVREITRHLAASTP

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP040915_2	2.1|1028929|23|NZ_CP040915|CRISPRCasFinder	1028929-1028951	23	NZ_CP040915.1	1028965-1028987	1	0.957
NZ_CP040915_2	2.1|1028929|23|NZ_CP040915|CRISPRCasFinder	1028929-1028951	23	NZ_CP040915.1	1029001-1029023	1	0.957
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP040915.1	667215-667246	2	0.938
NZ_CP040915_5	5.2|1058774|53|NZ_CP040915|CRISPRCasFinder	1058774-1058826	53	NZ_CP040915.1	1057321-1057373	2	0.962

1. spacer 2.1|1028929|23|NZ_CP040915|CRISPRCasFinder matches to position: 1028965-1028987, mismatch: 1, identity: 0.957

agcgtcagccgacgacgcggcgc	CRISPR spacer
agcgtcaggcgacgacgcggcgc	Protospacer
******** **************

2. spacer 2.1|1028929|23|NZ_CP040915|CRISPRCasFinder matches to position: 1029001-1029023, mismatch: 1, identity: 0.957

agcgtcagccgacgacgcggcgc	CRISPR spacer
agcgtcaggcgacgacgcggcgc	Protospacer
******** **************

3. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to position: 667215-667246, mismatch: 2, identity: 0.938

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
cccgcgccgccacgcccggagccggcaccgcc	Protospacer
** **.**************************

4. spacer 5.2|1058774|53|NZ_CP040915|CRISPRCasFinder matches to position: 1057321-1057373, mismatch: 2, identity: 0.962

tccacggacaactccaccaacgtgctggcgcacgactccaacgtggagatcgg	CRISPR spacer
tccacgaacaactccatcaacgtgctggcgcacgactccaacgtggagatcgg	Protospacer
******.*********.************************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP011920	Burkholderia cenocepacia strain ST32 plasmid pBCEN1232, complete sequence	170590-170614	2	0.92
NZ_CP040915_2	2.1|1028929|23|NZ_CP040915|CRISPRCasFinder	1028929-1028951	23	NZ_CP044329	Methylocystis rosea strain BRCS1 plasmid unnamed1, complete sequence	149440-149462	3	0.87
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NC_008704	Mycobacterium sp. KMS plasmid pMKMS02, complete sequence	10261-10289	3	0.897
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	CP000385	Mycobacterium sp. MCS Plasmid1, complete sequence	205313-205341	3	0.897
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP015597	Mycobacterium sp. YC-RL4 plasmid pMYC1, complete sequence	229412-229440	3	0.897
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NC_008704	Mycobacterium sp. KMS plasmid pMKMS02, complete sequence	10261-10289	3	0.897
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	CP000385	Mycobacterium sp. MCS Plasmid1, complete sequence	205313-205341	3	0.897
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP015597	Mycobacterium sp. YC-RL4 plasmid pMYC1, complete sequence	229412-229440	3	0.897
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	MK494117	Mycobacterium phage Miramae, complete genome	39447-39471	3	0.88
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	MK494129	Mycobacterium phage AvatarAhPeg, complete genome	39785-39809	3	0.88
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	MF919498	Mycobacterium phage Cindaradix, complete genome	39631-39655	3	0.88
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	384210-384234	3	0.88
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	719723-719749	3	0.889
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP035710	Sphaerotilus natans subsp. sulfidivorans strain D-507 plasmid pSna507_unt10, complete sequence	103677-103701	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	1465476-1465500	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	708182-708206	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	524781-524805	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_LR594691	Variovorax sp. WDL1 plasmid 3	7364-7388	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NC_018696	Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence	119999-120023	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP032695	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence	2520493-2520517	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NC_017957	Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence	607989-608013	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	340373-340397	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	309390-309414	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	579019-579043	4	0.84
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	KX579975	Mycobacterium phage Mundrea, complete genome	40011-40035	4	0.84
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP011920	Burkholderia cenocepacia strain ST32 plasmid pBCEN1232, complete sequence	170588-170617	4	0.867
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_012521	Rhodococcus opacus B4 plasmid pROB02, complete sequence	129345-129371	4	0.852
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_020062	Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence	1409693-1409719	4	0.852
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_015378	Burkholderia gladioli BSR3 plasmid bgla_3p, complete sequence	31735-31761	4	0.852
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	AP018698	Arthrobacter sp. MN05-02 plasmid plasmid1 DNA, complete genome	48919-48945	4	0.852
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NZ_AP014579	Burkholderia sp. RPE67 plasmid p1, complete sequence	862238-862264	4	0.852
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	720853-720879	4	0.852
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP018096	Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence	26947-26973	4	0.852
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	543072-543098	4	0.852
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NC_047816	Ralstonia phage RS-PI-1, complete genome	34483-34509	4	0.852
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NC_031230	Gordonia phage Yvonnetastic, complete genome	13965-13991	4	0.852
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	74426-74457	5	0.844
NZ_CP040915_3	3.2|1057471|29|NZ_CP040915|CRISPRCasFinder	1057471-1057499	29	NZ_CP029835	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence	7601-7629	5	0.828
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NC_019959	Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence	129126-129154	5	0.828
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	10242-10270	5	0.828
NZ_CP040915_5	5.4|1058924|29|NZ_CP040915|CRISPRCasFinder	1058924-1058952	29	NZ_CP029835	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence	7601-7629	5	0.828
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NC_019959	Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence	129126-129154	5	0.828
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	10242-10270	5	0.828
NZ_CP040915_9	9.1|3813286|25|NZ_CP040915|PILER-CR	3813286-3813310	25	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	491810-491834	5	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	451977-452006	5	0.833
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	436219-436248	5	0.833
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	436209-436238	5	0.833
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NC_013193	Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence	88286-88315	5	0.833
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NC_013193	Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence	103939-103968	5	0.833
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP014519	Sinomonas atrocyanea strain KCTC 3377 plasmid pSA01, complete sequence	54675-54701	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP019608	Tessaracoccus flavescens strain SST-39T plasmid unnamed, complete sequence	28232-28258	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP025510	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvD, complete sequence	85190-85216	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP025510	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvD, complete sequence	190583-190609	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	540787-540813	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP026928	Agrobacterium tumefaciens strain 1D1609 plasmid pAt1D1609b, complete sequence	182982-183008	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_LR134450	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 8, complete sequence	70601-70627	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	735464-735490	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3102098-3102124	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_023283	Streptomyces sp. FR1 plasmid pFRL3, complete sequence	322635-322661	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_002575	Agrobacterium rhizogenes plasmid pRi1724 DNA, complete sequence	155375-155401	5	0.815
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_KY000038	Agrobacterium rhizogenes strain 1724 plasmid pRi_1724, complete sequence	201678-201704	5	0.815
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NZ_CP045296	Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence	859225-859251	5	0.815
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	MN857473	Teseptimavirus S2B, complete genome	898-924	5	0.815
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NC_008703	Mycobacterium sp. KMS plasmid pMKMS01, complete sequence	138092-138118	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP021033	Rhizobium sp. NXC14 plasmid pRspNXC14c, complete sequence	537733-537759	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP010727	Phaeobacter inhibens strain P88 plasmid pP88_b, complete sequence	39269-39295	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP034153	Rhodococcus sp. NJ-530 plasmid unnamed1, complete sequence	47701-47727	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1679227-1679253	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP022192	Yangia pacifica strain YSBP01 plasmid unnamed2, complete sequence	2400-2426	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1655862-1655888	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417876	Uncultured Caudovirales phage clone 3F_6, partial genome	42526-42552	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417995	Uncultured Caudovirales phage clone 7F_19, partial genome	10158-10184	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417869	Uncultured Caudovirales phage clone 3S_4, partial genome	1978-2004	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417877	Uncultured Caudovirales phage clone 9F_7, partial genome	23384-23410	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417838	Uncultured Caudovirales phage clone 9S_4, partial genome	3810-3836	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417878	Uncultured Caudovirales phage clone 8S_7, partial genome	52860-52886	5	0.815
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	MF417848	Uncultured Caudovirales phage clone 10F_2, partial genome	2015-2041	5	0.815
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	710417-710445	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	69487-69515	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	357090-357118	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	618904-618932	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	349714-349742	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	698894-698922	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP023977	Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.2, complete sequence	46728-46756	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	696407-696435	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	694568-694596	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032324	Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence	513541-513569	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	469693-469721	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	18075-18103	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1682150-1682178	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	183787-183815	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	MG663585	Streptomyces phage ToriToki, complete genome	30191-30219	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	MG663583	Streptomyces phage Percastrophe, complete genome	30129-30157	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	MG663584	Streptomyces phage Romero, complete genome	30188-30216	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	241574-241602	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	255591-255619	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	650815-650843	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	362269-362297	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	544408-544436	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	9113-9141	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	697249-697277	6	0.793
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	450216-450244	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	710417-710445	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	69487-69515	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	357090-357118	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	618904-618932	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	349714-349742	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	698894-698922	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP023977	Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.2, complete sequence	46728-46756	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	696407-696435	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	694568-694596	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032324	Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence	513541-513569	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	469693-469721	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	18075-18103	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1682150-1682178	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	183787-183815	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	MG663585	Streptomyces phage ToriToki, complete genome	30191-30219	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	MG663583	Streptomyces phage Percastrophe, complete genome	30129-30157	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	MG663584	Streptomyces phage Romero, complete genome	30188-30216	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	241574-241602	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	255591-255619	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	650815-650843	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	362269-362297	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	544408-544436	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	9113-9141	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	697249-697277	6	0.793
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	450216-450244	6	0.793
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	MK494117	Mycobacterium phage Miramae, complete genome	39444-39473	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	MK494129	Mycobacterium phage AvatarAhPeg, complete genome	39782-39811	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	MF919498	Mycobacterium phage Cindaradix, complete genome	39628-39657	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	708180-708209	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	MN103533	Mycobacterium phage Weirdo19, complete genome	41094-41123	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	340370-340399	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NC_014120	Paraburkholderia sp. CCGE1002 plasmid pBC201, complete sequence	282299-282328	6	0.8
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_LR594691	Variovorax sp. WDL1 plasmid 3	7361-7390	6	0.8
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_013207	Alicyclobacillus acidocaldarius subsp. acidocaldarius DSM 446 plasmid pAACI02, complete sequence	61939-61965	6	0.778
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_004574	Ruegeria sp. PR1b plasmid pSD25, complete sequence	7859-7885	6	0.778
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP022421	Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-6, complete sequence	47847-47873	6	0.778
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	MT536174	Stenotrophomonas phage vB_SmaS-AXL_3, complete genome	25387-25413	6	0.778
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	174786-174812	6	0.778
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NZ_CP013054	Sinorhizobium americanum CCGM7 plasmid C, complete sequence	932645-932671	6	0.778
NZ_CP040915_10	10.2|3813696|27|NZ_CP040915|CRISPRCasFinder	3813696-3813722	27	NZ_CP011274	Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence	1854-1880	6	0.778
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	KU998235	Gordonia phage Bowser, complete genome	14919-14950	7	0.781
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP031079	Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence	272263-272294	7	0.781
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP016463	Bosea sp. RAC05 plasmid pBSY19_1, complete sequence	155124-155155	7	0.781
NZ_CP040915_3	3.2|1057471|29|NZ_CP040915|CRISPRCasFinder	1057471-1057499	29	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1073556-1073584	7	0.759
NZ_CP040915_3	3.2|1057471|29|NZ_CP040915|CRISPRCasFinder	1057471-1057499	29	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	2553751-2553779	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	933863-933891	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	105054-105082	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	252476-252504	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	795983-796011	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP045095	Streptomyces sp. GY16 plasmid unnamed1, complete sequence	29383-29411	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NZ_CP042999	Aquisphaera giovannonii strain OJF2 plasmid pOJF2_2, complete sequence	4421-4449	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	MT024859	Gordonia phage DumpsterDude, complete genome	1490-1518	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	KY697807	Microcystis phage MACPNOA1, complete genome	1046-1074	7	0.759
NZ_CP040915_3	3.4|1057570|29|NZ_CP040915|CRISPRCasFinder	1057570-1057598	29	NC_027348	Delftia phage RG-2014, complete genome	28533-28561	7	0.759
NZ_CP040915_5	5.4|1058924|29|NZ_CP040915|CRISPRCasFinder	1058924-1058952	29	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1073556-1073584	7	0.759
NZ_CP040915_5	5.4|1058924|29|NZ_CP040915|CRISPRCasFinder	1058924-1058952	29	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	2553751-2553779	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	933863-933891	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	105054-105082	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	252476-252504	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	795983-796011	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP045095	Streptomyces sp. GY16 plasmid unnamed1, complete sequence	29383-29411	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NZ_CP042999	Aquisphaera giovannonii strain OJF2 plasmid pOJF2_2, complete sequence	4421-4449	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	MT024859	Gordonia phage DumpsterDude, complete genome	1490-1518	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	KY697807	Microcystis phage MACPNOA1, complete genome	1046-1074	7	0.759
NZ_CP040915_5	5.6|1059023|29|NZ_CP040915|CRISPRCasFinder	1059023-1059051	29	NC_027348	Delftia phage RG-2014, complete genome	28533-28561	7	0.759
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NC_018696	Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence	119997-120026	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	KX579975	Mycobacterium phage Mundrea, complete genome	40008-40037	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	447778-447807	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	500615-500644	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP032685	Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence	939134-939163	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	883883-883912	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP032690	Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence	940133-940162	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	384208-384237	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	CP048300	Salmonella enterica subsp. enterica serovar Schwarzengrund strain WAPHL_SAL-A00527 plasmid pN1566-3, complete sequence	44030-44059	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	CP048302	Salmonella enterica subsp. enterica serovar Schwarzengrund strain WAPHL-SAL-A00375 plasmid p28945-1, complete sequence	95679-95708	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP028479	Klebsiella pneumoniae strain 2e plasmid unnamed1, complete sequence	16635-16664	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013525	Rhizobium phaseoli strain R744 plasmid pRphaR744c, complete sequence	57752-57781	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013554	Rhizobium phaseoli strain N931 plasmid pRphaN931b, complete sequence	57659-57688	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP020951	Rhizobium sp. CIAT894 plasmid pRheCIAT894d, complete sequence	70719-70748	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013588	Rhizobium phaseoli strain N161 plasmid pRphaN161c, complete sequence	57421-57450	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013560	Rhizobium phaseoli strain N841 plasmid pRphaN841c, complete sequence	57678-57707	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013577	Rhizobium phaseoli strain N671 plasmid pRphaN671c, complete sequence	62616-62645	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013549	Rhizobium phaseoli strain R611 plasmid pRetR611b, complete sequence	62616-62645	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013534	Rhizobium phaseoli strain R650 plasmid pRphaR650b, complete sequence	62616-62645	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NC_011368	Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG201, complete sequence	69459-69488	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013545	Rhizobium phaseoli strain R620 plasmid pRphaR620c, complete sequence	62610-62639	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013565	Rhizobium phaseoli strain N831 plasmid pRphaN831b, complete sequence	57659-57688	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP013571	Rhizobium phaseoli strain N771 plasmid pRphaN771c, complete sequence	62616-62645	7	0.767
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP018077	Sulfitobacter sp. AM1-D1 plasmid unnamed1, complete sequence	51105-51134	7	0.767
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	700945-700974	7	0.767
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	927152-927181	7	0.767
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3322179-3322208	7	0.767
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	885974-886003	7	0.767
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	347605-347634	7	0.767
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	253188-253214	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	676058-676084	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	372489-372515	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	176572-176598	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	JX163858	Caulobacter phage phiCbK, complete genome	2962-2988	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NZ_CP014514	Frondihabitans sp. PAMC 28766 strain SR6 plasmid 1, complete sequence	136310-136336	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555147	Caulobacter phage Ccr34, complete genome	205312-205338	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555145	Caulobacter phage Ccr29, complete genome	215432-215458	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555143	Caulobacter phage Ccr2, complete genome	208579-208605	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_019410	Caulobacter phage CcrKarma, complete genome	210979-211005	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555146	Caulobacter phage Ccr32, complete genome	204872-204898	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_019407	Caulobacter phage CcrMagneto, complete genome	208388-208414	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555144	Caulobacter phage Ccr5, complete genome	207626-207652	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	KY555142	Caulobacter phage Ccr10, complete genome	208104-208130	7	0.741
NZ_CP040915_10	10.1|3813636|27|NZ_CP040915|CRISPRCasFinder	3813636-3813662	27	NC_019411	Caulobacter phage CcrSwift, complete genome	208650-208676	7	0.741
NZ_CP040915_10	10.3|3813756|27|NZ_CP040915|CRISPRCasFinder	3813756-3813782	27	NZ_CP017427	Methylobacterium sp. XJLW plasmid unnamed1, complete sequence	25346-25372	7	0.741
NZ_CP040915_3	3.2|1057471|29|NZ_CP040915|CRISPRCasFinder	1057471-1057499	29	NC_013160	Rippkaea orientalis PCC 8802 plasmid pP880201, complete sequence	61313-61341	8	0.724
NZ_CP040915_5	5.4|1058924|29|NZ_CP040915|CRISPRCasFinder	1058924-1058952	29	NC_013160	Rippkaea orientalis PCC 8802 plasmid pP880201, complete sequence	61313-61341	8	0.724
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP035710	Sphaerotilus natans subsp. sulfidivorans strain D-507 plasmid pSna507_unt10, complete sequence	103675-103704	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	1465474-1465503	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	524779-524808	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP032695	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence	2520491-2520520	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NC_017957	Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence	607987-608016	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	579017-579046	8	0.733
NZ_CP040915_9	9.3|3813284|30|NZ_CP040915|CRISPRCasFinder	3813284-3813313	30	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	309387-309416	8	0.733
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	NZ_CP023519	Burkholderia cepacia strain FDAARGOS_388 plasmid unnamed1, complete sequence	172789-172818	8	0.733
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	NZ_CP007745	Burkholderia cepacia ATCC 25416 plasmid unnamed, complete sequence	196704-196733	8	0.733
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	NZ_CP022081	Burkholderia cepacia strain FDAARGOS_345 plasmid unnamed1, complete sequence	152392-152421	8	0.733
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	NZ_CP012984	Burkholderia cepacia ATCC 25416 strain UCB 717 plasmid pBC25416	99228-99257	8	0.733
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	NZ_CP034556	Burkholderia cepacia ATCC 25416 plasmid unnamed1, complete sequence	202408-202437	8	0.733
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP054616	Azospirillum oryzae strain KACC 14407 plasmid unnamed2, complete sequence	310507-310538	9	0.719
NZ_CP040915_9	9.4|3813347|30|NZ_CP040915|CRISPRCasFinder	3813347-3813376	30	MN336501	Pseudomonas aeruginosa strain 164130 plasmid p4130-KPC, complete sequence	33921-33950	9	0.7
NZ_CP040915_1	1.1|667176|32|NZ_CP040915|CRISPRCasFinder	667176-667207	32	NZ_CP029777	Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence	316983-317014	10	0.688
NZ_CP040915_9	9.5|3813410|30|NZ_CP040915|CRISPRCasFinder	3813410-3813439	30	NZ_CP029833	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence	120011-120040	10	0.667

1. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP011920 (Burkholderia cenocepacia strain ST32 plasmid pBCEN1232, complete sequence) position: , mismatch: 2, identity: 0.92

atctgcaggccgagctcggccggca	CRISPR spacer
atctgcaggccgagctcgaccggta	Protospacer
******************.****.*

2. spacer 2.1|1028929|23|NZ_CP040915|CRISPRCasFinder matches to NZ_CP044329 (Methylocystis rosea strain BRCS1 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.87

agcgtcagccgacgacgcggcgc	CRISPR spacer
gccatcagccgacgacgcggcgc	Protospacer
. *.*******************

3. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NC_008704 (Mycobacterium sp. KMS plasmid pMKMS02, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

4. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to CP000385 (Mycobacterium sp. MCS Plasmid1, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

5. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP015597 (Mycobacterium sp. YC-RL4 plasmid pMYC1, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

6. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NC_008704 (Mycobacterium sp. KMS plasmid pMKMS02, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

7. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to CP000385 (Mycobacterium sp. MCS Plasmid1, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

8. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP015597 (Mycobacterium sp. YC-RL4 plasmid pMYC1, complete sequence) position: , mismatch: 3, identity: 0.897

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaccacgacgtcgtggacatcgaggaggc	Protospacer
*** ****** *****************.

9. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to MK494117 (Mycobacterium phage Miramae, complete genome) position: , mismatch: 3, identity: 0.88

atctgcaggccgagctcggccggca	CRISPR spacer
ccctgcaggccgagctcgaccggca	Protospacer
 .****************.******

10. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to MK494129 (Mycobacterium phage AvatarAhPeg, complete genome) position: , mismatch: 3, identity: 0.88

atctgcaggccgagctcggccggca	CRISPR spacer
ccctgcaggccgagctcgaccggca	Protospacer
 .****************.******

11. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to MF919498 (Mycobacterium phage Cindaradix, complete genome) position: , mismatch: 3, identity: 0.88

atctgcaggccgagctcggccggca	CRISPR spacer
ccctgcaggccgagctcgaccggca	Protospacer
 .****************.******

12. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 3, identity: 0.88

atctgcaggccgagctcggccggca	CRISPR spacer
agctgcaggccgagcgcgaccggca	Protospacer
* ************* **.******

13. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 3, identity: 0.889

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
acgcctcgtcgatgaagagcacacccc	Protospacer
************ ** ********** 

14. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP035710 (Sphaerotilus natans subsp. sulfidivorans strain D-507 plasmid pSna507_unt10, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
gcctgcaggccgacctcggccggcg	Protospacer
..*********** **********.

15. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
tgctgcaggccgagctgcgccggca	Protospacer
  **************  *******

16. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
agctgcaggccgagctcggcctgac	Protospacer
* ******************* *  

17. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
tgctgcaggccgagctgggccgcca	Protospacer
  ************** ***** **

18. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_LR594691 (Variovorax sp. WDL1 plasmid 3) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
atctggaggccaagctcggccgggc	Protospacer
***** *****.***********  

19. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NC_018696 (Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
atctgctggccgagttcggccggac	Protospacer
****** *******.********  

20. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP032695 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
tcctgcaggccgagctcggcggcca	Protospacer
 .****************** * **

21. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NC_017957 (Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
acgggcaggccgagatcggccggca	Protospacer
*.  ********** **********

22. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
agctgcaggccgagctcggcctgac	Protospacer
* ******************* *  

23. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
atctgcaggcagagctcggccagag	Protospacer
********** **********.* .

24. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
gccggcaggctgagctcggccggca	Protospacer
..* ******.**************

25. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to KX579975 (Mycobacterium phage Mundrea, complete genome) position: , mismatch: 4, identity: 0.84

atctgcaggccgagctcggccggca	CRISPR spacer
ccctgcaggccgagctcgaccgtca	Protospacer
 .****************.*** **

26. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP011920 (Burkholderia cenocepacia strain ST32 plasmid pBCEN1232, complete sequence) position: , mismatch: 4, identity: 0.867

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gcatctgcaggccgagctcgaccggtaccg	Protospacer
* ******************.****.***.

27. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_012521 (Rhodococcus opacus B4 plasmid pROB02, complete sequence) position: , mismatch: 4, identity: 0.852

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
ctacctcgtggaggacgagcacacccg	Protospacer
 ..****** *****************

28. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_020062 (Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence) position: , mismatch: 4, identity: 0.852

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
aaggctcgtcgaggacgagcaaacgcg	Protospacer
* * ***************** ** **

29. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_015378 (Burkholderia gladioli BSR3 plasmid bgla_3p, complete sequence) position: , mismatch: 4, identity: 0.852

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
aggcctcggcgaggacgagcacatgcg	Protospacer
* ****** **************. **

30. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to AP018698 (Arthrobacter sp. MN05-02 plasmid plasmid1 DNA, complete genome) position: , mismatch: 4, identity: 0.852

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
cgtgatcgccaaggaggacggcgacga	Protospacer
 ***************** **** * *

31. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NZ_AP014579 (Burkholderia sp. RPE67 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
cgtgatcgccaaggcgcaaggcgtcga	Protospacer
 ************* * ******** *

32. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 4, identity: 0.852

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
cgtgatcgccaaggcgcaaggcgtcga	Protospacer
 ************* * ******** *

33. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP018096 (Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence) position: , mismatch: 4, identity: 0.852

caccctcgacgccgaggagggcatcga	CRISPR spacer
gcgcctcgtcgccgaggagggcatcga	Protospacer
   ***** ******************

34. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 4, identity: 0.852

caccctcgacgccgaggagggcatcga	CRISPR spacer
gcgcctcgtcgccgaggagggcatcga	Protospacer
   ***** ******************

35. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NC_047816 (Ralstonia phage RS-PI-1, complete genome) position: , mismatch: 4, identity: 0.852

caccctcgacgccgaggagggcatcga	CRISPR spacer
gatcctcgacggcgaggaggccatcga	Protospacer
 *.******** ******** ******

36. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NC_031230 (Gordonia phage Yvonnetastic, complete genome) position: , mismatch: 4, identity: 0.852

caccctcgacgccgaggagggcatcga---	CRISPR spacer
taccctcgacgccgaggagg---tcgaacg	Protospacer
.*******************   ****   

37. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.844

--ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
acccggcat--ccacgaccggagccggcagcgcc	Protospacer
  ******.  ***** ************ ****

38. spacer 3.2|1057471|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029835 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence) position: , mismatch: 5, identity: 0.828

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atcgccgacaactccaccagcctcgacgc	Protospacer
* * * *************.********.

39. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NC_019959 (Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence) position: , mismatch: 5, identity: 0.828

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcacgacgtcgtggacgtcgaggagga	Protospacer
**  ****** *******.********* 

40. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.828

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gccgagggcggcatggacatcgaggaggt	Protospacer
* *.* *.****.****************

41. spacer 5.4|1058924|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029835 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence) position: , mismatch: 5, identity: 0.828

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atcgccgacaactccaccagcctcgacgc	Protospacer
* * * *************.********.

42. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NC_019959 (Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence) position: , mismatch: 5, identity: 0.828

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcacgacgtcgtggacgtcgaggagga	Protospacer
**  ****** *******.********* 

43. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.828

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gccgagggcggcatggacatcgaggaggt	Protospacer
* *.* *.****.****************

44. spacer 9.1|3813286|25|NZ_CP040915|PILER-CR matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.8

atctgcaggccgagctcggccggca	CRISPR spacer
ccttgcaggccgagctcggccgtga	Protospacer
 ..*******************  *

45. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 5, identity: 0.833

ggatctgcaggccgagctcggccggcacca-	CRISPR spacer
tgatctgcaggtcgggctcggcc-gcgccag	Protospacer
 **********.**.******** **.*** 

46. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

ggatctgcaggccgagctcggccggcacca-	CRISPR spacer
tgatctgcaggtcgggctcggcc-gcgccag	Protospacer
 **********.**.******** **.*** 

47. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

ggatctgcaggccgagctcggccggcacca-	CRISPR spacer
tgatctgcaggtcgggctcggcc-gcgccag	Protospacer
 **********.**.******** **.*** 

48. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NC_013193 (Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence) position: , mismatch: 5, identity: 0.833

ggacctcgcggccggagtccggcgc-ccgca	CRISPR spacer
agacctcgtggccggagtccggcacgctgc-	Protospacer
.*******.**************.* *.** 

49. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NC_013193 (Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence) position: , mismatch: 5, identity: 0.833

ggacctcgcggccggagtccggcgc-ccgca	CRISPR spacer
agacctcgtggccggagtccggcacgctgc-	Protospacer
.*******.**************.* *.** 

50. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP014519 (Sinomonas atrocyanea strain KCTC 3377 plasmid pSA01, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
caacctcgtcgcggtcgagcacacccg	Protospacer
  .******** ** ************

51. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP019608 (Tessaracoccus flavescens strain SST-39T plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
gcagctcgtcgaggtcgagcacccccg	Protospacer
.*. ********** ******* ****

52. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP025510 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvD, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
aggcctcgtcgaggacgagcaacgtcg	Protospacer
* *******************   .**

53. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP025510 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvD, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
aggcctcgtcgaggacgagcaacgtcg	Protospacer
* *******************   .**

54. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
atgcctcgtcgatgaagagcacaccgc	Protospacer
*.********** ** *********  

55. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP026928 (Agrobacterium tumefaciens strain 1D1609 plasmid pAt1D1609b, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
acgcctcgtcgaggacgatcaggcttg	Protospacer
****************** ** .*..*

56. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_LR134450 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 8, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
tgggctcgtcgaggacgagcacccgcg	Protospacer
  * ****************** * **

57. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
gcgcctcgtcgaggtcgcgcacactgg	Protospacer
.************* ** ******. *

58. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
aggcctcgtcgaggaagagcacgccgt	Protospacer
* ************* ******.**  

59. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_023283 (Streptomyces sp. FR1 plasmid pFRL3, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
gggcctcgtcggcgacgagcacaccgg	Protospacer
. *********. ************ *

60. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_002575 (Agrobacterium rhizogenes plasmid pRi1724 DNA, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
acgcctcgtcgaggacgatcaggctgg	Protospacer
****************** ** .*. *

61. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_KY000038 (Agrobacterium rhizogenes strain 1724 plasmid pRi_1724, complete sequence) position: , mismatch: 5, identity: 0.815

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
acgcctcgtcgaggacgatcaggctgg	Protospacer
****************** ** .*. *

62. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP045296 (Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
gaggatcgccaaggaggcaggcgtcgc	Protospacer
*. ************** *******  

63. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to MN857473 (Teseptimavirus S2B, complete genome) position: , mismatch: 5, identity: 0.815

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
ccagatcgccagcgaggaaggcgtcca	Protospacer
   ********. **************

64. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NC_008703 (Mycobacterium sp. KMS plasmid pMKMS01, complete sequence) position: , mismatch: 5, identity: 0.815

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
ggcgatagccaaggaggaaggcggtga	Protospacer
**.*** **************** . *

65. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP021033 (Rhizobium sp. NXC14 plasmid pRspNXC14c, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
ggcgatcgtcgccgaggagggcatcga	Protospacer
 .*  *** ******************

66. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP010727 (Phaeobacter inhibens strain P88 plasmid pP88_b, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
ggcccgcgacgccgaagagggcatcgg	Protospacer
 .*** *********.**********.

67. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP034153 (Rhodococcus sp. NJ-530 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
gaccgtcgacgccgacgagggcatccg	Protospacer
 *** ********** ********* .

68. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
cgacctcgaccccggggagggcatcgg	Protospacer
*. ******* ***.***********.

69. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022192 (Yangia pacifica strain YSBP01 plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caccatcgaggccgaggagggcaccag	Protospacer
**** **** *************.*..

70. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
cgacctcgaccccggggagggcatcgg	Protospacer
*. ******* ***.***********.

71. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417876 (Uncultured Caudovirales phage clone 3F_6, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

72. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417995 (Uncultured Caudovirales phage clone 7F_19, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

73. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417869 (Uncultured Caudovirales phage clone 3S_4, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

74. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417877 (Uncultured Caudovirales phage clone 9F_7, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

75. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417838 (Uncultured Caudovirales phage clone 9S_4, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

76. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417878 (Uncultured Caudovirales phage clone 8S_7, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

77. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to MF417848 (Uncultured Caudovirales phage clone 10F_2, partial genome) position: , mismatch: 5, identity: 0.815

caccctcgacgccgaggagggcatcga	CRISPR spacer
caacctcgacgccgaggagggtgacaa	Protospacer
** ******************.. *.*

78. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

79. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

80. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

81. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

82. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

83. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

84. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023977 (Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ctccacgaccgcgtggagatcgaggaggc	Protospacer
  * ***** ******* **********.

85. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

86. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

87. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032324 (Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

88. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

89. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

90. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

91. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

92. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to MG663585 (Streptomyces phage ToriToki, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaggagtacggcgtggacgtcgaggagga	Protospacer
** .*  ***********.********* 

93. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to MG663583 (Streptomyces phage Percastrophe, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcagcacggcgtggacgtcgaggagga	Protospacer
**  *  ***********.********* 

94. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to MG663584 (Streptomyces phage Romero, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcagcacggcgtggacgtcgaggagga	Protospacer
**  *  ***********.********* 

95. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

96. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

97. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
caccgcggcggcgtggacatcgaggatct	Protospacer
 ** .**.******************  *

98. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gacggcgacggcgtggacatcgacgtcat	Protospacer
***..****************** *  .*

99. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

100. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

101. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

102. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

103. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

104. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

105. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

106. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

107. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

108. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

109. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023977 (Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.2, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ctccacgaccgcgtggagatcgaggaggc	Protospacer
  * ***** ******* **********.

110. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

111. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
agctacgacggcgtggacatcgtcgagga	Protospacer
..* ******************  **** 

112. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032324 (Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

113. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

114. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

115. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

116. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

117. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to MG663585 (Streptomyces phage ToriToki, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gaggagtacggcgtggacgtcgaggagga	Protospacer
** .*  ***********.********* 

118. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to MG663583 (Streptomyces phage Percastrophe, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcagcacggcgtggacgtcgaggagga	Protospacer
**  *  ***********.********* 

119. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to MG663584 (Streptomyces phage Romero, complete genome) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gagcagcacggcgtggacgtcgaggagga	Protospacer
**  *  ***********.********* 

120. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

121. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

122. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
caccgcggcggcgtggacatcgaggatct	Protospacer
 ** .**.******************  *

123. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gacggcgacggcgtggacatcgacgtcat	Protospacer
***..****************** *  .*

124. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

125. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

126. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accgagggcggcatggacatcgaggaggt	Protospacer
. *.* *.****.****************

127. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 6, identity: 0.793

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ttccacgactgcgtggacagcgaggagat	Protospacer
  * ***** ********* *******.*

128. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to MK494117 (Mycobacterium phage Miramae, complete genome) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
caccctgcaggccgagctcgaccggcaccc	Protospacer
 . .****************.******** 

129. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to MK494129 (Mycobacterium phage AvatarAhPeg, complete genome) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
caccctgcaggccgagctcgaccggcaccc	Protospacer
 . .****************.******** 

130. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to MF919498 (Mycobacterium phage Cindaradix, complete genome) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
caccctgcaggccgagctcgaccggcaccc	Protospacer
 . .****************.******** 

131. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
cgagctgcaggccgagctcggcctgaccta	Protospacer
 ** ******************* *  *.*

132. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to MN103533 (Mycobacterium phage Weirdo19, complete genome) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggcggtgctggtcgagctcggccggcaccg	Protospacer
**   *** **.*****************.

133. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
cgagctgcaggccgagctcggcctgaccta	Protospacer
 ** ******************* *  *.*

134. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NC_014120 (Paraburkholderia sp. CCGE1002 plasmid pBC201, complete sequence) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggatctgcaggccgacctcggaaagcgcct	Protospacer
*************** *****  .**.** 

135. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_LR594691 (Variovorax sp. WDL1 plasmid 3) position: , mismatch: 6, identity: 0.8

ggatctgcaggccgagctcggccggcacca-	CRISPR spacer
acatctggaggccaagctcggccgg-gccat	Protospacer
. ***** *****.*********** .*** 

136. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_013207 (Alicyclobacillus acidocaldarius subsp. acidocaldarius DSM 446 plasmid pAACI02, complete sequence) position: , mismatch: 6, identity: 0.778

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
acgcctcgtcgagcacgagcactttta	Protospacer
************* ******** ....

137. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_004574 (Ruegeria sp. PR1b plasmid pSD25, complete sequence) position: , mismatch: 6, identity: 0.778

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
atgcctcgtcgaggacgagcgcaatgc	Protospacer
*.******************.** .  

138. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022421 (Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-6, complete sequence) position: , mismatch: 6, identity: 0.778

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
ctgcctcgtcgaggacgagcgcaacgc	Protospacer
 .******************.** *  

139. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to MT536174 (Stenotrophomonas phage vB_SmaS-AXL_3, complete genome) position: , mismatch: 6, identity: 0.778

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
caagctcgtcgaggacgaggacacgcg	Protospacer
  . *************** **** **

140. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.778

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgacctcgacgaggtcgagcacaccct	Protospacer
  .***** ***** *********** 

141. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013054 (Sinorhizobium americanum CCGM7 plasmid C, complete sequence) position: , mismatch: 6, identity: 0.778

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
ggtgatcgccaaggcggcaggcggtgg	Protospacer
************** ** ***** . .

142. spacer 10.2|3813696|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP011274 (Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence) position: , mismatch: 6, identity: 0.778

ggtgatcgccaaggaggaaggcgtcca	CRISPR spacer
ccggatcgccaaggaggccggcgtccc	Protospacer
   **************  ******* 

143. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to KU998235 (Gordonia phage Bowser, complete genome) position: , mismatch: 7, identity: 0.781

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
gcggcaccgcggcgcccggagccggggcggca	Protospacer
 ********* .************* .* ** 

144. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to NZ_CP031079 (Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence) position: , mismatch: 7, identity: 0.781

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
ccgctgccgccgcgcgcggagccggcaccagc	Protospacer
*** ..*****.*** *************. *

145. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to NZ_CP016463 (Bosea sp. RAC05 plasmid pBSY19_1, complete sequence) position: , mismatch: 7, identity: 0.781

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
gcggcaccgcgacgcccggcgccgatgcggcc	Protospacer
 ********* ******** ****...* ***

146. spacer 3.2|1057471|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 7, identity: 0.759

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atgccggacatctccaccatcctcgaccg	Protospacer
*  .****** ******** *******  

147. spacer 3.2|1057471|29|NZ_CP040915|CRISPRCasFinder matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.759

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atgccggacatctccaccatcctcgaccg	Protospacer
*  .****** ******** *******  

148. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gacaacgacggcatggccatcgaccccga	Protospacer
************.*** ******    * 

149. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ctagacgacggcatggtcatcgaggaggg	Protospacer
   .********.*** *********** 

150. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ggcaacgacggcggggacaccgaggttcc	Protospacer
*.*********** *****.*****   .

151. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ggcaacgacggcggggacaccgaggttcc	Protospacer
*.*********** *****.*****   .

152. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP045095 (Streptomyces sp. GY16 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gtaggcgtcggcgtggacgtcgaggaggg	Protospacer
*  ..** **********.********* 

153. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP042999 (Aquisphaera giovannonii strain OJF2 plasmid pOJF2_2, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
tggatcgacggcggggacatcgaggaagg	Protospacer
 . * ******** ************.* 

154. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to MT024859 (Gordonia phage DumpsterDude, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accatcgacggcgtgcacatcgaggtagg	Protospacer
. ** ********** ********* .* 

155. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to KY697807 (Microcystis phage MACPNOA1, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
tacgacgacggcgtcgacatcgagcgcat	Protospacer
 **.********** ********* . .*

156. spacer 3.4|1057570|29|NZ_CP040915|CRISPRCasFinder matches to NC_027348 (Delftia phage RG-2014, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gccaacgacggcgtgggcaccgaggcctg	Protospacer
* **************.**.*****    

157. spacer 5.4|1058924|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 7, identity: 0.759

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atgccggacatctccaccatcctcgaccg	Protospacer
*  .****** ******** *******  

158. spacer 5.4|1058924|29|NZ_CP040915|CRISPRCasFinder matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.759

aactcggacaactccaccaacctcgacgt	CRISPR spacer
atgccggacatctccaccatcctcgaccg	Protospacer
*  .****** ******** *******  

159. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gacaacgacggcatggccatcgaccccga	Protospacer
************.*** ******    * 

160. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ctagacgacggcatggtcatcgaggaggg	Protospacer
   .********.*** *********** 

161. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ggcaacgacggcggggacaccgaggttcc	Protospacer
*.*********** *****.*****   .

162. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
ggcaacgacggcggggacaccgaggttcc	Protospacer
*.*********** *****.*****   .

163. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP045095 (Streptomyces sp. GY16 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gtaggcgtcggcgtggacgtcgaggaggg	Protospacer
*  ..** **********.********* 

164. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NZ_CP042999 (Aquisphaera giovannonii strain OJF2 plasmid pOJF2_2, complete sequence) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
tggatcgacggcggggacatcgaggaagg	Protospacer
 . * ******** ************.* 

165. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to MT024859 (Gordonia phage DumpsterDude, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
accatcgacggcgtgcacatcgaggtagg	Protospacer
. ** ********** ********* .* 

166. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to KY697807 (Microcystis phage MACPNOA1, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
tacgacgacggcgtcgacatcgagcgcat	Protospacer
 **.********** ********* . .*

167. spacer 5.6|1059023|29|NZ_CP040915|CRISPRCasFinder matches to NC_027348 (Delftia phage RG-2014, complete genome) position: , mismatch: 7, identity: 0.759

gacaacgacggcgtggacatcgaggaggt	CRISPR spacer
gccaacgacggcgtgggcaccgaggcctg	Protospacer
* **************.**.*****    

168. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NC_018696 (Paraburkholderia phenoliruptrix BR3459a plasmid pSYMBR3459, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggatctgctggccgagttcggccggacatg	Protospacer
******** *******.********   ..

169. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to KX579975 (Mycobacterium phage Mundrea, complete genome) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
caccctgcaggccgagctcgaccgtcaccc	Protospacer
 . .****************.*** **** 

170. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ccgacagcagtccgagctcggcccgcacca	Protospacer
  . * **** ************ ******

171. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggacctgcaggccgagcgcggcctcgccta	Protospacer
***.************* *****    *.*

172. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032685 (Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggatctgcaggccgagcgcgggctcgccta	Protospacer
***************** *** *    *.*

173. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
agcgcggcaggccgaggtcggccagcaccg	Protospacer
.*  * ********** ******.*****.

174. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032690 (Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ggatctgcaggccgagcgcgggctcgccta	Protospacer
***************** *** *    *.*

175. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gaagctgcaggccgagcgcgaccggcaggc	Protospacer
*.* ************* **.******   

176. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to CP048300 (Salmonella enterica subsp. enterica serovar Schwarzengrund strain WAPHL_SAL-A00527 plasmid pN1566-3, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gcatacctcggccgcgctcggccggcacca	Protospacer
* ** . . ***** ***************

177. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to CP048302 (Salmonella enterica subsp. enterica serovar Schwarzengrund strain WAPHL-SAL-A00375 plasmid p28945-1, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gcatacctcggccgcgctcggccggcacca	Protospacer
* ** . . ***** ***************

178. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP028479 (Klebsiella pneumoniae strain 2e plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gcatacctcggccgcgctcggccggcacca	Protospacer
* ** . . ***** ***************

179. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013525 (Rhizobium phaseoli strain R744 plasmid pRphaR744c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
agatctgcaggccaagctcggcatggcgat-	Protospacer
.************.******** .***. . 

180. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013554 (Rhizobium phaseoli strain N931 plasmid pRphaN931b, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

181. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP020951 (Rhizobium sp. CIAT894 plasmid pRheCIAT894d, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

182. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013588 (Rhizobium phaseoli strain N161 plasmid pRphaN161c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

183. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013560 (Rhizobium phaseoli strain N841 plasmid pRphaN841c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
agatctgcaggccaagctcggcatggcgat-	Protospacer
.************.******** .***. . 

184. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013577 (Rhizobium phaseoli strain N671 plasmid pRphaN671c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

185. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013549 (Rhizobium phaseoli strain R611 plasmid pRetR611b, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

186. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013534 (Rhizobium phaseoli strain R650 plasmid pRphaR650b, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

187. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NC_011368 (Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG201, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
cgcgcggcaggccgagctcggacagcacct	Protospacer
 *  * *************** *.***** 

188. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013545 (Rhizobium phaseoli strain R620 plasmid pRphaR620c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

189. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013565 (Rhizobium phaseoli strain N831 plasmid pRphaN831b, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

190. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP013571 (Rhizobium phaseoli strain N771 plasmid pRphaN771c, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggc-cggcacca	CRISPR spacer
cgatctgcaggccaagctcggcatggcgat-	Protospacer
 ************.******** .***. . 

191. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP018077 (Sulfitobacter sp. AM1-D1 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

ggatctgcaggccgagctcggcc-ggcacca	CRISPR spacer
ggatctgcaggcggagctgggcctgacgtt-	Protospacer
************ ***** **** *.*... 

192. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.767

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
cgatgccgcggccggggtccggcgccagct	Protospacer
 **. .*********.********** ** 

193. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 7, identity: 0.767

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
cgggcccggggctggagtccggcgcccgcc	Protospacer
 *. *.** ***.**************** 

194. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.767

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
acaggttgcggccgaagtcccgcgcccgca	Protospacer
. *  *.*******.***** *********

195. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 7, identity: 0.767

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
cgggcccggggctggagtccggcgcccgcc	Protospacer
 *. *.** ***.**************** 

196. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.767

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
cgatgccgcggccggggtccggcgccagct	Protospacer
 **. .*********.********** ** 

197. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgacctcgtcgaggacgagcaccgagg	Protospacer
  .*******************    *

198. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgacctcgtcgaggacgagcaccgagg	Protospacer
  .*******************    *

199. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgacctcgtcgaggacgagcaccgagg	Protospacer
  .*******************    *

200. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgacctcgtcgaggacgagcaccgagg	Protospacer
  .*******************    *

201. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to JX163858 (Caulobacter phage phiCbK, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

202. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP014514 (Frondihabitans sp. PAMC 28766 strain SR6 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cgtcctcgtcggggacgagcacacgga	Protospacer
   ********.************  .

203. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555147 (Caulobacter phage Ccr34, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

204. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555145 (Caulobacter phage Ccr29, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

205. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555143 (Caulobacter phage Ccr2, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

206. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_019410 (Caulobacter phage CcrKarma, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

207. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555146 (Caulobacter phage Ccr32, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

208. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_019407 (Caulobacter phage CcrMagneto, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

209. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555144 (Caulobacter phage Ccr5, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

210. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to KY555142 (Caulobacter phage Ccr10, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

211. spacer 10.1|3813636|27|NZ_CP040915|CRISPRCasFinder matches to NC_019411 (Caulobacter phage CcrSwift, complete genome) position: , mismatch: 7, identity: 0.741

acgcctcgtcgaggacgagcacacccg	CRISPR spacer
cctgaccgtcgaggacgagcacacctt	Protospacer
 *   .*******************. 

212. spacer 10.3|3813756|27|NZ_CP040915|CRISPRCasFinder matches to NZ_CP017427 (Methylobacterium sp. XJLW plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.741

caccctcgacgccgaggagggcatcga	CRISPR spacer
ctacctcgacgccgaggagggcgggcg	Protospacer
*  *******************.   .

213. spacer 3.2|1057471|29|NZ_CP040915|CRISPRCasFinder matches to NC_013160 (Rippkaea orientalis PCC 8802 plasmid pP880201, complete sequence) position: , mismatch: 8, identity: 0.724

aactcggacaactccaccaacctcgacgt	CRISPR spacer
aactctgacaactccaccaccctattaac	Protospacer
***** ************* ***    ..

214. spacer 5.4|1058924|29|NZ_CP040915|CRISPRCasFinder matches to NC_013160 (Rippkaea orientalis PCC 8802 plasmid pP880201, complete sequence) position: , mismatch: 8, identity: 0.724

aactcggacaactccaccaacctcgacgt	CRISPR spacer
aactctgacaactccaccaccctattaac	Protospacer
***** ************* ***    ..

215. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP035710 (Sphaerotilus natans subsp. sulfidivorans strain D-507 plasmid pSna507_unt10, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ccgcctgcaggccgacctcggccggcgcgt	Protospacer
  ..*********** **********.*  

216. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gctgctgcaggccgagctgcgccggcatgc	Protospacer
*   **************  *******.  

217. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
tctgctgcaggccgagctgggccgccatcc	Protospacer
    ************** ***** **.* 

218. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP032695 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
attcctgcaggccgagctcggcggccagct	Protospacer
.  .****************** * ** * 

219. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NC_017957 (Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
gcacgggcaggccgagatcggccggcaggt	Protospacer
* *.  ********** **********   

220. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
cggccggcaggctgagctcggccggcatgc	Protospacer
 *..* ******.**************.  

221. spacer 9.3|3813284|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 8, identity: 0.733

ggatctgcaggccgagctcggccggcacca	CRISPR spacer
ccatctgcaggcagagctcggccagagctg	Protospacer
  ********** **********.* .*..

222. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP023519 (Burkholderia cepacia strain FDAARGOS_388 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
ctgctgtccctgaaccgacgagctgctcct	Protospacer
*   ..*****  **************** 

223. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP007745 (Burkholderia cepacia ATCC 25416 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
ctgctgtccctgaaccgacgagctgctcct	Protospacer
*   ..*****  **************** 

224. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP022081 (Burkholderia cepacia strain FDAARGOS_345 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
ctgctgtccctgaaccgacgagctgctcct	Protospacer
*   ..*****  **************** 

225. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP012984 (Burkholderia cepacia ATCC 25416 strain UCB 717 plasmid pBC25416) position: , mismatch: 8, identity: 0.733

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
ctgctgtccctgaaccgacgagctgctcct	Protospacer
*   ..*****  **************** 

226. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP034556 (Burkholderia cepacia ATCC 25416 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
ctgctgtccctgaaccgacgagctgctcct	Protospacer
*   ..*****  **************** 

227. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to NZ_CP054616 (Azospirillum oryzae strain KACC 14407 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
tggcgatgaccacgcccggcgccggcaccccc	Protospacer
. *  *. .********** ********* **

228. spacer 9.4|3813347|30|NZ_CP040915|CRISPRCasFinder matches to MN336501 (Pseudomonas aeruginosa strain 164130 plasmid p4130-KPC, complete sequence) position: , mismatch: 9, identity: 0.7

cacgcatccctccaccgacgagctgctccg	CRISPR spacer
gcaacatcccatcaccgacgagctgctgga	Protospacer
   .****** .***************  .

229. spacer 1.1|667176|32|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029777 (Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.688

ccggcaccgccacgcccggagccggcaccgcc	CRISPR spacer
ccgacaccgccacgcccggcgccacggtgagc	Protospacer
***.*************** ***.  .. . *

230. spacer 9.5|3813410|30|NZ_CP040915|CRISPRCasFinder matches to NZ_CP029833 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.667

ggacctcgcggccggagtccggcgcccgca	CRISPR spacer
ccgagtcgccgccggagtccggcgccgcgg	Protospacer
  .  **** ****************   .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	725198 : 791602	60	Gordonia_phage(33.33%)	transposase,integrase,protease	attL 719298:719315|attR 791369:791386
DBSCAN-SWA_2	2072352 : 2083359	14	Microbacterium_phage(70.0%)	portal	NA
DBSCAN-SWA_3	3416932 : 3423215	7	Planktothrix_phage(33.33%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP040915|725198:791602|DBSCAN-SWA
CATGGCTCACGACAAGCTTGGGCCGGGCGAGCATGGCGAGATCTTCATCAAGCGGCACAAGAGCGGCAAGTTCCAGGCCCGTGTGCGCGTCCGGCTGTTCAACGGCGAGGAGACGCAAGTCTCCCGGAACCGCAAGACCGGTGCGGCGGCGCGGCTGGCGGTACAGGCCGAGATCGACACCTTGCTCAACGCGCCCAGGGGCTCGGCTCAGCTCAAGCCGGACAGCAGGGTCGGCCTGGCTGCCCGCCAGTGGATCGACGACCTGCGGCTGCAATCGACTTGGCCCAATCCGCCTCGGCGCCCACAGACGGTCGACGAGTACGAGCGGCTGTTGGGTACGCAACTGATCCCGAAGCTGAGCAAGTATCGGCTGAACGAGCTGACGACGGCGGTCTGCCAGGACTGGGTCAACTCGATCATCGAGGCGGGCAAGTCGGGCCCGTACGACATGGTCGTGACGGCAGCACAGGCACGTGGCGCGTTCAAGGCCGTGATTGATCGCGCGATCGTGCACGACGCGCTGCGGTACAACCCCATGGACAAGACCACCACCCCGAAGCGCAAGGTGCCTGATCCGAAGGCCATGACGGTGACCGACGTCTATCGCCTCCGGAAGGCGGTCCGTGACTGGGAGTGCGCGCGAGTCGGCCGACCCGGTCCGCCTCCCACCGGCCACGTTCCGGCGGCGATCGACGTGATGCTTGGCACCGGCTTGCGAATCGGTGAGGTGCTCGCACTCAACTGGGGGAAGGTCAACCTGAGCCGTGACGGGCTGCCGACCATCGCCGTGGACGCGACCCTCGTGGACATCAAAGGCCACGGCACGGTCCGCCAGGAGATGCCGAAGACCGACGCCGGCAAGCGGACCATCATCATCCCGAAGTTCACGGTCGAGTCGCTGGAGGCGATCCGGCCGCCCATCACCCGGCCGGATATGCCGCTGTTCCCCTCCCGGCGGTTCAGGGATGGTCGCGCATCGTTGAAGCCACAGACACCGCACAACGTTCGCCGGACGCTCCGTGCCGCGCTCGAGTTCGCGAACATGACGGGCGAGGTCCATCCGCACCTGCTGCGATCGACGGTCGCGACCTTCGTCGCGCGAGAGCGAGGGATGGCGGACGCCGCCGCCCTGCTCGGGCACAAGGTCAACGGTGGGGTCACGGTCCGGCACTACATCGAGCGGCTTCGGCTCGCACCCGACGCCTCGACCGTGCTGCAGGCCATGGTCGAGATTGGTGAGGAGGAAGCAGCCAAAGCGACCCACCAACGGACTACGGGTGCGGACGCCGCTCGTGCCGATGCGCCGGCAGTCACCGCCGCGAAGGTGGCGGTGGCCGGCGAGGACTCAGGTTGGTGACGAGTGATCAGGAGAGCTCCGAAGCCCGGCCGCTGACTGCCGGTCGGTGACGGGCTGTTCTGTGGGAGGTCCGGAGTCTCTGCGGTGGGCGTGAGTCACGCCCACCGTTCAGTGCTCCCCCGCGCGTGCGCCATACACCGACGGGAAGGGCAGGAACGCAACGTCGCTGCGGCGGCCACAAGTCGCGCGCACCGGCGAAGTTGACGGCGCCTGCCAACGCCCTACCTCTGGAAATGGTCAAACTCTCCATGCGCTCCACTATGGCGGCCGCGCGTACCTGTTTCCGTCCCCCCTGACCGCGTTCTCCCAGCGTCCCCCCGAGGGGAGACGCAGCAACAGTGCAGGTCGCAGAGCGTCCCCCACATCATGAAACGTATTGCGGCCGCGGTAAGGGATCTGCGCTGGGCTGCCCTCGGCCAAGCATTCGTAGGTGGTGACGGTCGAGAAGCTGAACACGAGCGACACGGTCGGACGGAGCGCGAAGCCGGACCGACTCGTGCGCGCGTTCCTCCAGAACCGTGCGCACGCGGCTAGGTTCACGTGAGCGTTCGAAAAGTTCGAGGTCGACGAGGACGTCGTCGGCCATGTGCACGGCCAACGCCTGTCCGCTTTGGCGCGCCACGCTGTGATCGGCACGCCGTGTGCTGGTGTGCTGCGCGCTTTGCGGCCGAGCCGCACGCGGGGAAGCTGATGGTCGCGCGGGCGGCGGTTGGCAATGCCGGTTGCACCACCGACTTGTCGGTCATGGCCGCCACGCCCCCTCACAGGCGAAGTTCGCCCGGGCCGGCTCATCGTCGTTCAGTGCGCCGTCCGCTGTCGTCGTCGCGAGCCCGACCTCATCGCCGGCCTCATCTCCGAAGCCCGCGGGCCGGTGCCCGACGACGTCCGCGCCGCGCTCGACGAACGACGCGACCTCATCGAAGCGCGCGCCCAGGCACTCGCCGAGTCCGCCGTCCGCCACCGTGCGCCCTGGGTCCTGCGGATCGGTGAGCCACCGCTTGACGGCACTGAACGGGCACGGTGGGTGCGGCAGTTGGCGGTCGTCGCCGCGTACCGCGACAGATACGGCGTCACCAGCCAGGACCCTCTCGGACCGGAAGCCGAGACCCTGGCTCAGCGACGCGATGCCGAGCGCGCTGCGGCGGCATTGCGCGGCGCCCGAGCCATCGCAGACACGAACACACCGAGAGGCATGAGCCCGTTGAGTGCGGGTCGCAAGATCGGGTAGCTGCTGACATACGTCGATTCGGACCAGTGCCCGATTCGACCGCCTTCCACTTACCCTCCACTTTGACTTCTCTGGCGCGGTTGCGGCGGCTCGGCCGTGCGACGCGCAGCGATCGGTGCCGGAGAGTCACGGCTGTCGCGGTGTGCGTCGCACACTACGCGAGCGGTGAACGTCGCCTGCAGCGTTGAGTGGGCTCGACCCGCTCCTGTGCGTCCACGAGTCGCCGAGTACCTCGGAGTGCCCGTCCGGACGATCTACGACTGGCGCCAGAGCGGGCACGGCGCGCGGGGCATCCGGGTCGGCCGGCACCTGAAGTTCGCCGTCTCCGACGTGGCCGCGTGGATCGACGCGCAGCGCGAGGCCACGCAGGACGGCCGCGATCGCGCTAAGGGGTGATCTGAGGTGGCGCGGCCCCGTACGCCGATCGCCACGTTCGGCGACATCGACTTCACCACCCTGGCGAACGGTCTGGTCCACGGCCCGGGGTGCCCTTCCGGGACCTTGACGGTCGGCTCCGCCGCGTCGAGGCCAGCGGCACGACCCGGAAGATGGCGGAGCACGCCTGAAGGAGGAGCTCGCCCGGTTGACGTCTGGCTCGAGGATCTCGATCCCGAGGGCAAGCTCGCGCCGAGCCACCAGAGCGCTCTACGAGCGGAACATGCGGCAACTGGTGCTGCCCGCCTTCCAGAACTACACGCTGCGGGAGATCAGCGTCCGTAAGGTCGAGAAGGTTCCTCAAGAGCATCGCCGTCCTGACCGTTGTCCTTTCAGCAAAGTGGCCAAAGTGGGCATAGATGGAGCAGGACAAGCTCAACGGTGTCAGGCTGTACCACCGCTGCCGGCGGCTCTGCTTCTTCGTCGCGTGCCGTGTCGGCCTCGGCGCTTGGCGGGGCAATCGATTCGGCGAGGGTTTCGGCCAGTTCGCGGACGGCGATGACGAACCGTGCGGGTTCCTGTCGTTCTTCTGTGATGGTGTGGCCGACGTTTAGGAGGTCGTCCAACATGGTGATGGTTTCGGGGCCCAGGTCCGCGTCGCTTCGTGCCCTCAGCACAGCGGCAATGTGGCCCAGGGCCTGCTCAGGTGTCATGAGAAGTCTCCCTGCCTTCGGTTTCCATTGCGGTGTCGGCGGCGACAAGGTGATCGCCTGGTGATTACTCGTCCGGGCATGAAGTCCGCGGTGGCGACGGTGGCGACGGTGGCGTAGCGGAGCAGGGCCGCCTGGCCTTGTACTACACCGATCCCGGCCCCACGGCAGTCGTCCCGGTCCGACATGCTGGAGCGCTTCAGGCTCACCGCCAACGTTGTCGACGTGGTCGCCCCCCGGAGCGTGACCGACGTGCGCCCGCGAAGCGCGCTAGCGCGCTGCGGCTTGCTCGTGCCTCTCGGCTTAGATCTCACCGCGGTGCTCCAGACCTCGGAGAGCCAGCCAGCCGAGGGGTACGGGTGCCCAGAAGGTCAGCTAGCCGGAAAAGCAGGGTGGTGGACAGGGCGGTGCCGTAGGGCATGCCGGCCACGGTTAGGCCACCCGTGAGTGCGAGCTCGATGGGGCCGATCCCGCCGGGGGAGGGGATGAGCGACCCGGCGGCGCTCGCGCCGAGATAGGTGATGGCGAGGGTCACCAGCGGCAGCGTGTCCCCGAACGCGGCGAGTGATGCGCCGAAGGCGGCGATATATCCGGCGCTCAGCAGCAGCCCACCGAGCGCTCCCAGAGCGACGCGGCTCGGGTGGCCGGTGAGCCACGAGAGCCGCGGCCCGAGCTGCGCCAGCGTGGGCCGGACCTTGGCCAGCGCCCACCGGCGGACCGGGGGCAGGGCGAGGGCGGCCATCAGTGCCATGGCCGCGCCGAGCACGACGATGACTAGCACCGGCGACGGCGCGGTCAGGGTTCCCACGGAGCCGGTGAGGAGCGCGGTGCTGACGAGCAGCAGCATGGTCATTAGGAACTGCATGAGCTGCGTTAGCCCGACCGTGGCAATTGCGACGGGCAGAGCGACTTGCCGGCGTTGGAGGAATCGAAGGTTCAGGCCCGCGGGTCCCACACCCGCTGGGACCACGAGAGCCAGCAGCGAGGCGGCGAGCTGGACCAGCGTGGTGCGCACCAGGCCCAGGCGCTCGGGGGAGAAGGCGACGAGGCCGAGGCTCGAGCCGAGGTAGGTGACCATTCCGAGCAGGAAGGCCGCGACCATCCAGCCGGGCCGGGCGCCGGAAATGGCGGAGGCAACGTCCTCGGAGCCGAGGCTGCCCATGAGCACCCAGGCCGCGACGCCGCCGACCACGACGAGCACGACTGTGCGTGGGCTGAACCGGTTGATGCGCGCCGGTTCGGTGGACGCGGTTGGGACCAGTTGCGCGGGGTTCCGGCGCAGGTCCTCCAGCAAGTGGCGACGAGGCCGGAGGGCAACCCTGGTGCTCGCGGGGAGCGCGACGGGCTGGACGAGCGGCGCCACAGCGGCGAGGTTCGCCCGGCCCAGGGAGCGGGTGGCGGAGGCGATAGCGCGGTCGGGGCCGGCGTGCACGGCGAGGAGGACGAGGGCCTGGGCGAGGTCGATGCGTTGCGCGAGTTCGGAAGCCAGGGTGTCGCCGTGGTCCCAGTGCGCGAGCCGCACGCGGCGGCCGGCGTCGACCAGGACCGACCGGGCGTCGAGGTCGTTGTGGCTCAGGCCGCGCCCGTGGGCCGCCCGCAGCTGCTGCCACACGTCGTCCAGCACGGTGTCGTCGAGCTCCTCGGCCGGCAGGTCGGCGAGGGGGCGCAGGCCAGGTATGTGCGCCGTGATCATGATGACCGAGTTGCGCGCTGCGGCGACGCCCACGAGCGGCGGTGTGCGCACCCCGGCGTGCTGTGCCCAGAGGATCATGAGGATGGTGTGGCCGGCATTCTCGCGCAGGTTCGATCCGCCGCGGCGGCGGAGTCCGCGGATGCGCAGCGTGTCCCAGAGCCCGCCGAGGTAGTCCAGGACCTGCCGGTCCCCATCGAGCACGGATATGTCGTAGCGCCGCTCCTCGGTGTCCCACGCGGCGTAGTGGCGGGCCCCGTCGCGGGCCCCGTCCTGGTCGGCGGCATCGGCCATCCCCGCGCGAGCTGCCACGGCGTCGGTGATCTCGTCCACGGTGATGCTGTCGCCCGGCGGACTCGTGCCCGCGCCGACGTCCTCGGGGATCGGCCGCGCCAAGCCGAACGGGCGGGGCTCGGGGTACCCGACCGGGGCCGAGGTCCGGACCCTCCACGCGACGGCGCGCACGCCGTCGGCGGGGACGTCCCGACGGAGGATCCGCACGGGGTCCAGGCCCGCCCGGCGGACGGCGCGCACCAGCGCCGGGCCGGATGCCCGGTCGGAGCCTGCGCCCAGGAGGTAGCGCAGCAACAGGCCGACGGCGTGCCCGAGCAGCACGAAGACCGCCGCGCCGGCCATCGTCTGCCTGCCCTGGATCACGGACACGCCGAGGACCACCCACAGCAGCGTCCAGGGCACCGCCCGGTGGCGCATGTCGCTGGCTGCCACGGTCAGCAACGCGGTCAACCCGGCTACGTAGGGGCTGGCTCCCACCAGCTCACTGCCTGCCGGGGCAGCCGGATCGAGGACGCCTTCGACGACGGTGAGGTGTCCGCCCAGCCGCAGGAGGACCACGGCCGCCAGCACGGAGGCGGCCGCGGCGAGAACCATCCCGGCTGCGGTGCGGAGGGCACGCCGGGAGACGGCGGCCACGAGGACGGCGGCCGGGACGAGGTACGCCGCGACACCCTCGAGGGCGGTCAGTGGGGCCAGGAGGAGGGAACGGACCACGGCCAGCGCCGTCGCGACATCTCCGCTCACCGCACGGGTGGTGCGGGGCGCATAGACGGCGAGCACCAGCACCGCGGCGATCCCCGCAAGGCTGAGTGTCAGGCCGACGAGGTCGCCCGGGCGGCGCAGCGGCACGGCTGGGACGTCGACCAGGAGGATGTCATGTGTCGGCGGGACCGGGGGCTCGGGCGGCCGGCGGTCCGTGCCGACGGCCGCGTCCGGAGTCATCAGGGTCATCCCGCGCCGCCTGCGGTGGCGGCGTCGCTGGGACCCGCTGCGGAGACCAGGACTGGGACCGAGACGTGCACGTCGCCGCGGTGGGCGAAGGTGAGCGTGACGGGGACGACGGTCCCAGCCCGCAAGGCCGGATCAGCGACGGTGACCCGCGCGTCCCCGGCGGCCAGGCCGACGGGCGTGGGCCGCTCCGTCGTGACGGTGACGGCGCCTGGAGTGCCCGCTCCGGCGGTGACCGTCGCCTGGCGGCCGTCGATCTTCGCGCCGACGAGCCGGTCCTCGGAGCCGTGGGTAATCACCAGGGCGCCGGCGAGTTCCCACGACGCCGGCGCCGGAGTACCGCTGGCTGCGGCCGTGGGCACGATGTACAGGTCGAGCATCTGAAGCCCGTGCGCCTGCCGCTGCACGCCGACGGCGACGACCTGGTGCAGGCCGACGAGGGACTCGGCGCCGTTGTGGAACCATGACAGCCCGACGGCGAAGACGACGCCGGCGAAGGCGGCCATCACCACGGCCGGCCATTTCTGGCGGGGCACCGGCGGGTGCTGGGCTCGCGTGGCCCCGCGGCCGAGTCGGCGGGGCGGCCGTGTGGCACGGTCCGGGACGTCGGGGCGGGCAGCGGTCAGGTCGTGCTGGTTCATCGCAAACCTCCGGAAGGTGATCCTTGTGCGGATGCTGCTGCGTCCGGCGATCGGCAGGTCGCCCGCCGCTGCTGTATGGACGTCCGGCGCTCTCGGTCACGACCTGGACGTCGGCTAGGGGCTCGCGTGGCGGGCCGCAAGTAGCAGCAGCGAGTCGCGGTCCCCGGTGTCGGGGCGGTGCGCGCGGTCGGTGGCCGAGCGCAGCTGATAAGGCACCGAGGTGACCACCACGCCGGGCTGGAACAGCAAGCGGCTCTTGATCCGCAGCGAGCTGTGGTTGTGCAGGGGCTGTTCCCACCACCGGCCGGCGACGCGCTGCGCGATCACGACGGTGATCACATCGCGGGGGCTGGTGCGGGGGTACGTCCTGACGTAGTCGACGACCGGTCGGGTGATCTCGCGGTAGGGGGAGTACAGGACGACCAGCGGGACGTCGACGTCGAGGTGATGGTCCGCCCAGGCTCGTTTGAGCTCTTCGGTCTCGTCCTGCTCGACCTCGACGGTGAGCGCCTCGAGGCTGGCTGGGTGGATCGCCCTGGCATAGGCCACCGCCTGGGCGGTCGGCAGGTTCAGCCCGGACACCAGCACGATGGCGTGGTTCCTCGCCGGGAGCGTGGGCTCCTCGTGCAGCGCGGTCTCCTCGCGCACCTTCTCGTAGTACCGGCTGATGTGGCGCATGAGCAGGAACAGTGCGGGCATGGCGACGCACACGATCCAGGCGCCGTGGCTGAACTTGGTCACCACGACGATGACCAGGACCAGGCCCGTGGTGACGGCGCCGAGGGCGTTGATCACCTGGCCCCGCCGGATGCGCTGGCGTTGCCGGTCGGTGGCGCGCGCCCGGTCCCGTTGCCAGCGTCGGACCATCCCGGCCTGAGCCAGGGTGAAGGACACGAAGACGCCGACAATGTAGAGCTGGATGAGCCGGGAGATGTCGGCGTCGAAGACGACGACCAGGAGACCGGCGGCCAGCGCCAGGACGATGATGCCGTTGCTGAAGACCAGCCGGTCCCTGCGGTGGTGCAGCTGGCGCGGCAGGTAGCCGTCGCGGGCGAGGAGAGAGGTCAGGACGGGGAACCCGTTGAAGGCGGTGTTGGCGGCGAGCACGAGGATGCCGGCCGTGGCCGCTTGGATGAATGCGAAGAGCGGCCCCGGGCCGAACACGGCGTCGGCGATCTGGGCGAGAGCGGTGGGCTCCACGTAGCCGGCGGGCGCGCCCAGGAGCCGTCCCGGTTCGTCGACCATCTGCACATGGGTGAGCAGGGCCAGCAGGGTGATGCCGCCGAACATGGTGGCCGAGAGGACGCCCATCACGGCGAGGGTGGTGGCAGCGTTGCGCGACTTGGGCGGCCGGAAGGCGGGGATGCCGTTGCTGACCGCCTCGACGCCGGTCAGGGCGGTGCATCCGGAGGCGAACGCGCGCAGCACGAGCACCACGAGGAGCAGACCTGGGAGGTGAGGCGCCGGCTGTACGTGGAAGTCGGCGCTGACGGCGTGCAGGTGCTGCCCGGTCATCACCCGCCAGGCCGCGACAGCAAACATCAAGAAGATGCCGGCGATGAACGCGTAGGTAGGAGCGGCGAAGCCGCGACCGGACTCCTTCAGCCCGCGGAGGTTGACCAGCATCAACAACAGCACGAACCCGAGCGAGAGGGCGACCGCGTGGCGGTTGAGTGCTGGGGCGTACGAGGTGATCGCGTCCACGCCGGCCACCATCGACACCGCCACGGTCAGCACGTAGTCGACCAGGAGCGCGGCGGCGGCGACCAGGCTGGCGCGCTCGCCGAGGGTGTCGCGGCTGACGATGTACGCCCCGCCCCCGCTTGGATAGGCGAAGCAGATCTGCCGGTACGAAGCGACGACGATGCCCAGGAGCACCAGGATCGCCAGGCCCACACCCCGGGTTAGGTGCAGCAGCATCGATCCGCCAAGCGCCAGCACGAGCAGGATCTCCTGGGTCGCGTACGCCACCGAGGAGATCGGGTCGCTGCAGAAGACGGGCAGCGCCAGCCTCTTGGGGAGCAGCTGCTGACCGAGGTTTTCGGTCCGCAGCGGCTGACCTACCAGCAGCCGTTTGGCCTCATTGGTCATGTGATCAACCTCGCAAACCGCGCATGAGAGGCCCATGAGAGATGGGCCCGGCCTGATGCTGGCGCCGGTACCCGGCAGGGTGCCTCTCGCTGGAGGCGTTCACCGGCTGGAGCTCGCGGGGGAGGGCGGCGCTCATGGGCTGGTCGCTGTGGCGGGGGCGGCGCTGCGCGAGCTGAAGTGCGCTGACCACCAGGGGGAAGTGGCTGAAGGCCTGCGGAGTGTTTCCAAGCTGGCGGCCCATCCGGGGGTCCCATTCCTCGCTGAGCAGCCCGACGTCGTTGCGCACGGCGAGCAGCCGTTCGAACAGCGCGATGGCGTCGTTCTCGCGGCCGGCATAGTGCAGGGCGTCGACCAGCCAGAAGGAGCACGCGAGGAAGACCCCCTCGCCCGCGGGCAGCCCGTCGTCAGCGGTCTCGGTGCGGTATCGCAGCACGAGCCCGTCCTGGGTCAGCTCGCGCTGGATCGCATCGATGGTGCCGAGCACGCGAGGGTCCGTGCCGGGCAGGAAGCCCACGCGCGGGATCAGCAGGAGGCTGGCGTCCAGTTCGGTGCCGCCGTAGGACTGCACGAACGTGCCACGTTCGTCGTTGTAGCCGTGGCTCAGGACGTCGGCGTGGATGTCGTCGCGAAGGTCTTGCCAGCGGCGCAGGGGGCCGGGGAGCCCGCTCTCGCGCACGGCGCGTGCCATGCGGTCGGCGGCGACCCAGGCCATGACCTTGGAGTGGGTGAAGTGGCGCCGCGGCCCGCGCATTTCCCACAGGCCGTTGTCGGGGTCCCGCCAGTGACCTTCCAGGTGGTCCATCAGTGCGACCTGCAGGTCCCAGGCGTCGTCATCGGCCGCCATGTTGGCCTGCCGGGCCAGGTGGAGCCCGTCGAGAACCTCGCCCCACACGTCTAGCTGGAACTGGCCTGCTGCGGCGTTGCCGGTGCGGACGGGGGTGGAGCCCTCGTAGCCGGCCAGCCACGGCAGGGGCGTCTCCGGCAGGCGGCGCGTGCCGTCGAGGCCGTACATGATCTGCAAGGTGCCGGGATCGCCGGCCACGGCACGGAGCAGCCACTCGCGCCAGGCGGTCGCCTCCTCGGCGTAGCCGGCCGCGAGCAGCGCCTGCAGGGTGAAGGTGGCATCGCGCAGCCAGCTGTAGCGGTAGTCCCAGTTGCGCGGCCCGCCGGGCTGTTCGGGCAACGATGTGGTGACCGCGGCGACGATGCCGCCGGTGGGCGCGTAAGTGAGTGCCTTGAGCACAATGAGGGAGCGTTGGACCGCGTCGCGCCAGCGGCCGGTGGCCGAGGAGCGTGCGGACCACCGTTCCCAGAAGTCGACGGTGTCGCGCAGTGCCTGCTCGGGGTCGAGGGGGTCGGGCGTGGCCAGGTGGCTCGGCGCCCAGGTCAGCACGAACGGGACGGTCTGGCCGGAGCGAACGACGAACTCGGAGACGGTGCGGTTGTCCTGCCCGCGCAGCGGCGCCGGGGTGCGCAGCCAGGCCGCGTCCGGACCCGCCACCGCCTCGATCGCGCCGCCGATGTTGCGCACCCACGGGACGACGTGGCCGTAGTCGAAGCGCAGACGCAGTTCCCCGGACATCGGGACGGTGCCGCGCACGCCCTGCACCAGGCGCACGACGTGGGGCGTTTCACCCCTGGGTGGCATGAAGTCGACGACCCGGACGCTTCCCGTGGGGGTGTCCCACTCGGTTTCCAACACCAGGGTGTCGCCGCGGTAGCGCCGCCGGCTGCAAGGCCCGCCGGCGGCGGGGGCAAGCAGCCACCGGCCCGCCTCGGCGGTGTCGAGCAGCGCGGCGAAACAGGCGCCGGAGTCGAACCGGGGCACGCACATCCAGTCGATCGAGCCCTCCCGGCTGACCAGGGCAGCGGTGTGCAGGTCGCCTAGGAGGGCGTAGTCCTCAATCCCGGTCATGGTTTCGGCTCCATCGGCTCTGGGCGGCGAGCTGCCCTGACGGAGCCAGCGTGCGACGCGGCGGATGAGAGCCCCGTGAGAAGCAGGGACGTCCGCGTCTTCCGGTTCTGATGGCGGTGCGTCCGCACGTCACCATGGCGTCAGGCGTCGGCCCATGTGGTGTGCCCCGGCCATGGCTGCGAGCAGGACCAGGAGCGCGAGGATCATCCCGGCCAGTCCTAGGCTCTGCTCGGCCTGGGCGCAGCGCGGCGAGATACCCGATGCCCGCAACTGCGACGCCCCACAGCGCCCCTCCCAAGACGTTGAAGACGACGAATCGCCGGTAGGGCAGCCCGCTGGCGCCGGCGACACAGGGGACCACGGCGCGCAGCAACGCTGCCCAGCGGCCAATCAGCACCGCCGGCGCGCCCCACCTCTGGACGACGGCTTCGGCGGCGGCCAGGTGCCGTCGTGCGCGGTCCGGGGCGCGAGCGTCCAGCTTCGGCTCCAGCCGGGCCCCGACGGCGTAGCCGATGTTGTCCCCGACGACCGCGCCCAGCACCGCGGCGGCCATCACGACGACCAAGGGCACCTTGCCGAGGTGGGCCAGCACGCCACCGAGCAAAACGGCGATCTCGCCCGGGACCAGCAGGCCGAGCGTGTCGAGGCTTCCAGCGCCGGAAGGGCAAAACGATCAGGAGCAGCACCCACGGGGGCACCGCCGCGAGCTCGTGGACCAGTGCGGTCATGGGAAACCATCCAAGGGGTGACCAGTCAGCAGGGCGCATCTCATGGCGGCTCGTTCCCGTGGGGGCCACCAGCGCTCACGCCGATGCCCGGTGGTACTACGGGCACGAGGTCCGCGGCGGCCCTGGAGTAGTTGTCATGCCTGCCTCGCTTCTCGCTTCTCAATGAGGTGGGTGCCATCGTCGGGGTTAGCGTGCCGCGGAGGTATGAGATCGCGGTGAGAGCCGGCCCTGGGGTCAGGCGAGGATGTTCACCGCCCGGGCCACCACGAGGCCCACCGTGACGAAGGACAGCAGCTCTTGGGCGAGCATCGCCATCTTCACCCGCCTGGACAGCGGCAGGGTGTCGGTGGGGCTGAACGCGGTGGAGTTGGTGAAGCTGATGTAAAGGTAGTCGGCGAAGGTCGGCGTCCAGTCGGTCTGCCCCATGCTCATCTGCGGGAAGAGGAGCTCCGGTGGGCGGTCACGGCCCACGCTGCGGGCGTGCGGGCCGCCCTGGTCGATCTCCCAGAGCACGAGCGCGAAGACGACGACGTTGGTCAGCCACACGCCGACTGCGGCGACGATGAGCTCGCGCCCGTTGGCTCGGCCGCCGGCAAGGAGCAGCCGGGTGATGGCGACGAGGGAGACGGCGTTGGCCGCGGCGATCACGCCGACCAGGGCCAGGGACAACGCTCGTGCGTCGCGCGACTCCCGGGTCAGCCGCGTCGGGTTGGCCAGCAGCAGCCCGACGAGCAGCGCCACCTCCAGGGCCGGAACGATCCAGCGGGGTCCGGACGTGAGGCGGTCGGGCAGGGCCAGGTGCAGGCCGGCCGCGGCGGCCACGGCGGCCGCGGCGCCCCACCGTGACTCTCCCTCGGTCCGGCGCCCTCGGTGCACGTCGCCGCCGCTCAGCCTTCGGGGTCGAGCCGGTAGCCCGCGCCCCGGATGGTGCGGATGGTGTCTCGGCCGAAGGGACGGTCCACCTTGTCGCGCAGGTAGCGCACGTAGACGTCGACGACGTTGGAGGCGCCGTCGTAGGCGAAGTCCCAGACGTGGTCGATCAGGGCGGTGCGGCTGTGCACCTCGCCGGGGCGGCGCATCAGCTCGTGCAGGAGCGCGAACTCCTTCGGCGACAAGGCGATGTCCACATCCCCGCGGCGAACGAGCCGTGATGCGGGGTCGAGCATCAGGTCACCGACCTGAAGCACCGCCGGTCGTTCCAGCGGGTCGCGCCGGGTGAGCGCGCGGATCCGGGCGTAGAGCTCGGCAAGGGCGAACGGCTTGGTCAGGTAGTCGTCGGCGCCGGCATCGAGGCCTCGGACGCGGTCCGGTACGGCGTCGCGGGCGGTCAGCATGAGCACCGGCACCCAGCGACCCTCGGCGCGGATGCGGCGACACACCTCGAAGCCGTCGGGCGGGGGGATCATGGCGTCGAGCACTACCGCGTCGTAGGCGTTCTCCGACACGCTCCACAGAGCCTCGTCGCCGGTGGCGGCCACGTCCACCGCGTATCCCTCGCGCTGGAGGCTGCGCGCCAGCAGGGACCTCATGCTCGGCTCGTCCTCGACGACCAGCAGCCGCATGGTCATGAGCCTAGACACCTTCGCGCCCTCACGTTCGGCCTCGGCCTCCGCCGCTGCTGGGCGGTCCCACATGTTCTTCGGAGCGCTCCGTCTCGACGTCGCGCCGGCCGCCGTCTCCTCGCGTCGCCTGTGGCGTCCTGGTGGTTTCCACGAGGGCGGACAGCCGGGCGAGGTCCGCGTGCAGCCGGCCCATGTCGTCGCGGAGCTCATCGACCGCTGCTGCTCGTCGCCGGTCCCACTCCAGGTCGTACAGCGCTACCTGCGCGGCCATGCGGTTGGCGCGACGGGCCTGAAGGAGCACCAGCTGCAGGTCGCAGACCATCAGCCCGGACAGGCCGAGGGTGAGCAGGGCCACCGGGCCCTGGGCACGGTCGTGCCAGACGGCCACCGCGATGCCCAGGGCGACCAGGATGGGCAGTGACGCCACGAGCACCCACGAGCCGAGGACATCACCGGCCCGCTCGATCGCGCGTTCACCGGCGCTTCTCCGCTCTGCCCGCACCGCGGGGTGGAGCTCCCAGCCATGCCGATGTCGCAGACTGCCCATCTTGGCCTTTCGATCAACGCGGCGGCGCCGCGGCCCTCCGAGACAGCTGCTGTTCGTCATGGCGCAACGGTGCCGCGCCGAGCATGAGGGGACCATGAGAGGCTCCTGGCAAGAGCGCTGGGGACGGCCGTGTGGGCCGTCGCCGACGGACCTGAGTTTGCTCACGGCGGGCCGGTTCGGTCACGTCCGTTTCCCACACGAGGGTCCGGGTGTTCAGGGGACGCCTCCGTCGTGATCCTGGAGGTCCGGAAGGCCCGTCGAAGCGGGGGTGAGGTGCCGTGCGACTGATGCCGCACTCCCTGGGTGCGCGGGTGACGTTGGTGTTCGCGGTGGGGGCGGCAGCGGCTCTGGTGCTGTGCCTGGCCCTGCTGTACCTGATCCTGAGCCGGCAGCTGGTCACGGCGCTCGATGACGACTTGCGTGCCCGCAGCGCGGACCTGGTCGCGGCCGTCGCCGCCGGTGACGTGGAGGTCGTGGTCCGGGATCCCCTGGCGCAACTCTACGGCCCGGAGGGCGCGGTGATCGCCGGGTCCGCAGCACTGGGGGACAGCCGGCTCCTGTCACCGGACGGGGTGCACCGCGTCCGGGCTGAGGAGCTGCGGACCCGGCTCCTGGCGCGCGGGGAGGAGGCGCCCACTGCGGTGCGGGTGCTCTCGCAGCGGGTCGGCGGCGACGGGGTGCTCAGCGTGGCGGTGTCGGTGGAACCGCTGCACGAGGCCCGCAGACGGTTGCTCGAGGTCCTTGTCCTCGCCGCCCCGCTGCTGGTCGCCGTCCTCGCGGTTGCCGGCTGGCTGGTGGTCCGGGCGGCGCTGCGGCCGGTGGACGTCCTGACCCGCGAGGCGGCCGCGATCTCCACCTTCGAGGCCGCCCGCGGCCTGCCGCCGGTGCCCGGCGACGATGAGATCGCCCGCCTGGCCCGCACCCTCGACGCCATGCTCCGCCGGCTGCGGGTCGCCTTTGAACGCGAGCGGGCCTTCGTCGACGACGCCAGTCACGAGCTGCGTACCCCGATCGCCGTGGTGCTCGGCGAGCTGGAGCTGGCGCTGTCCGCGGTCGACGACCCCGAAGAGGTCGAACGGTCCCTGCGGGCGGCACTGGGCGAGGCCCAGCGGCTCTCCCGGCTGGCCGAGGACCTCCTGCTGTTGGCCCGCGCGCAGGCCGGGTCCCTGGTCATCCGCCGCGAGCCGGCCGACCTGCTCGATCTTGCCGTCACCGAGGCCGGGCGCCTGGCACCGGTGCTGGGGGCGCGCATCCAGGTGTCCGGCGAGCCGGCCACCGTGGTCGGGGACCCCGACCGGCTCCGGCAGGTGCTCACCAACCTGGCGCGCAACAGCGCCGCCGCAGGGGCGACCACGGTGCGCGTGCGCGTGGCCCGCGACCAGGCCCGGGCCATCCTCGAGGTTGCCGATGACGGACCCGGCTTCCCGCCGGGCGCCCGTGACCAGGCCTTCGAACGGTTCGTCCGCGGCACCGGCCCACGCACCCCGGGCGGCTCGGGAGCGGGACTGGGCCTGTCGATCGTGCGGGCCATCGTCACCGCCCACGGTGGCACCGTCGAAGCGAGGAACGGGGACCCGCTCGGCGGGGCGGTGGTCACCGCACGGTTGCCCCTCGCCTGACCAGAGACCGGCCCCTGGCGCATCACGTGGCGCCTGGGCCGGTCTCGACCGCGGTCGTGCGCTCGGGCACTTACGGACCGGCGCTGGTGACGGGAGCGCCGGCGAGGGTTCCGGAGGTCGACGGGGGCCCGCCCGGGGCAGCGCCGGGTCGGATCCAGCCGGTGGGCGGGCGGTTCGCCGCCTTTGGTGATTCCGCGGAGCGGCGGGCGGCTCGGTGCAGCCACCAGGTGAGTGCCATCAGGGCGGTGAAGCTGAGCAGGCCGATCGCGAGGTCGCCGTGTCCGATGGCTGCGGCGCTGTCCCATCCGGCGTGCAGGCAGATGGCGGCGACTAGGACGGCGAGGAAGCGCAGTGAGGCGAGGCCGCGGCGGCGGGCGTCGGGCACGGCGAACAGCGCGGCGCAGGCCAAGCCGGTCCAGGCGGCATGGCCGCCGAGGCTGCCCAGGCCTCGCAGCGCCAGCAGGTGGTCGACCGGCTGCAGGTTGCCGCCGGTGCGCAGCAGCACGGTGAAGGCGTATCCCATCGTCTCGACGGCGGCGAACGCGCTGCCCACGGCGACGCCGAGGACCAGCCCGTCCACGGCGCGCGGCCGGGTGTGCCGCCAGGCCAGCCAGGCCAGGAATACCGCCGGCACGGCGAGCTTCGCGCACTCCTCGATGAGGGCCACGATCGCGAACGGCAGCCAGCCCAGGGTGCGGGCGGCGTCGAACTCCAGGGTCCCGGCGAGGATGCCGCCGAGAACACCGCCCAGCACGGCAGCGGTGAGGATGTTCGGCAACGACAGGTGGGTGTGCGCGACCGCGGTGACGAAGGTGGTCAGCGTCACCGGGACGATGGCGGCGCCCAGGAGCAGCAGGCACGGAAGGAAGATCGGGTCACCCGTGTCCAGCGTGACGGCGCCGACGGCGCCGAAGAGCACGAGCCCGGTGACCAGGACGGCGAGCCAGCCCAGGCGGGGCCAGGATGCCGGTGTGGTGGAAGTGCGATGCGCGAGGGCGTTCACTGGATTCTCCTAGAGGTGGTGTCTCGGAATGGATGCGTGTCGGAGGACGGGTCGGCGAGCCATGCAGCGAAGCCGGAGGGCACAGGCCCCTCGGGCGACCCCGTGGCGACCCTGTGGAGGATGTCGTAGACGATGGCCCCGTCGACCGTCTCCGTCTCGAGCAGCAGGTGGGTGACCTTGTCCAGCGCGCTGCGGTGTCCGGCCAGCAGGGCGGCGGCACGTTCGTCGGCCTCGTTGAGGAGCCGGGTAACCTCGGCGTCGACCCGCCGTTGCGTGTCGTCCGCGTACGGGCGATCGGGTCCGCCGTCCAGGCGGCTTGTCGGCGAGGGCGGATATGCCACCGGGCCCAGCCGGGACAGGCCGTACTCGAGGACCATGCGCTGGGCCAGCTGGGTGGCTCCGGCGAGGTCGTCGGCCGCCCCGGTCGAGGCCTGCCCGAGGACCACCAGCTCGGCGGCCCGTCCGGCCAGCCGGACGGTCAGCAGGTCCGTGAGGTACTGCTCGGAGTAGAGGCGCCGCTCGTCCACCGGCAGCTGGTGGGTGGCGCCCAGTGCCGTCCCCGCGGGCAGGATGGTGATCTTCGCGACCGGGTCGGCGGTCGGGGACAGTGCCGCCACGACGGCATGGCCCGACTCGTGCACGGCGACCCGGCGCCGCTCGTCCGGCAGCAGGGCGCTGGTCTCGGGACGGCCCAGGATCAGCCGGTCGCGGGCGGCATCAAAGTCGGCGGCGCGAATCGTCCTCCTGTTCGCCCGCGCCGCGCGCAGCGCCGCTTCGTTGACCAGGTTGGCTAGGTCGGCGCCACTAAACCCCGGGGTTCCGCGGGCAAGGGCGTGCAGGTCCACGTCCGCGCTGAGGTGCTTGTCGCGGGTGTGGACGGCCAGGATGCGTTCCCGATCGGCCAGGGCGGGCAGCGGAACCGTGACCTGGCGGTCGAAGCGCCCGGGCCGCAGCAGCGCGGGGTCCAGGATCTCGGGGCGGTTGGTGTTCGCCAGCACGACGACCGAGGTGTTCTGAGTGAACCCGTCCATCTCCGCGAGGAGTTGGTTGAGGGTCTGCTCGCGCTCGTCGTTCCCGGCGATGCCGGCCACGCCGCGGCGACCGCCGATCGCGTCGATCTCGTCGATGAAGACGATCGCGGGCGCGCTGGCGCGGGCCTGGGCGAAGAGGTCCCGCACGCGGGATGCGCCCAGCCCGGCGAAGATCTCGACGAAGCTGCTGCCGGTGGCCGCGTAGAAGGGCACGTTGGCCTCGCCGGCGACCGCGCGCGCCAGCAGGGTCTTGCCGGTGCCCGGCGGTCCCACGAGCAGCACGCCGCGCGGGCCCCTGGCGCCGGTCTCGAGGTAGCGGTCCGGGTGCTGGAGGAAGTCCACGACCTCCCGCACCTCCTCCTTGGCCCCGTCGTAGCCCGCGACGTCATCGAACGTGGTGTGCGGCCGCTCGGCGTCGGAGACCTTGGCCTTCGTGCGGAAGGTGCTGGCCAGCCCACGGCGCCCCATCCAGACCATGGCGCCGATCAGCAGCAGCATGGGCAGGAACGACGCCACCACCTGGGCGAGTGAGCCGCCCTGCTGGAAGAGTGAGCCGCCCTGCTGGAAGGCCGACACGTGCACCCCCGCCTGCTCAAGCTGGTGGGACAGGTCGGTCGTGGTCAGCGCCCACACCGGTGCCTGAGTGACGAAGTCCTTGCCGCTGGTCAGCACGCCGGTGACCTGCCCCTGGCTGCCCACCGCGACCGAGGACACGTCATGGTGCCGTACGTCCGACAGGAACGTGCTGTAGGACAGGTGCTCCGTGCCCTGTGAGCCGAGGAGCCCGGGACCGAAGGACAGCAAGAGAAGCAGCACCACGCCGAACGGCAGCGCCCACCGTGGCCACATCGGCTGCCACCTGGGAGAGCCGCCGGGTCCGGGCCGACGATCATGGCCCGTCCCGGACCGAGCGGTCGGACGGTCCGTCCGCTGTTGGCTCGATGGTGCTTGGAACGTTGGCATGGTGGGCTCCTTCGGGTGCGTCGTCGCGATCCACCCTGCTAAGCCACCGATGAGAAGCCGATGAGAAGCGGGGGCGGCCGCCAACAGCGCGACGGCGCTGCCGGGAAGTGCCCGCCCAGACGCCAGTTCTCCTCAGGCCGACAGCAGTCGGCGGGCCGCAGCGGCGATGTGCGCCGCGTCGATCCCTGCCCACGCCGGCAATTCCTGTCCCGAGCCGGAGCCTGGCATGTCGCGCATGGCCGGGTCTCGAGGTGGCCTAAACCAAGCCGGCGGACAGCAACTGCCACGGCGGCCGCGAGGGGAGCATCATCGTGGGGCCCGACCCACCATGCGCCCGACGAGCGGGAGCTCCGTGAGCCCTTCGGCGTCGGCCATCGCCAAGCCCTGCCCGGCAAGAAGGTCGAGGGTCCCTACGGCGGCGAAGCGCGGCACCCAGCGTGGGCCGTACTTGGCGTTGAAGCGCCACAGCGACTCGATCTGCATGTTGTTCGACGCCCGCCGGAGCAACTGGCGCGCGAGCCGCGCCGTGGCGGTTACGCCGTTGTCGCCGGCGACGATGCGGCGTCCGACCGCGAAGTTGAGGCCGAGCGCGGTGCCACCGGCCTGTCGAACCCACCAGATCGTCTCGACGATAAGGAAGTCCATGATCCCGTTGGGAAGGTCCGGCGCCATGCTGCGGCGCATGACGTCGAGCGACCACCCGGGCAGCTTCGTGGCGGGCACCCACTGGCTGAATGCCTGGGCCCGCCCGGCGGCGTCGCGCGCGACGGCCACCACAACGCCAGTGTCGGCGGGGTCGAACAGGCGCGAGAGGGTCATCGAGAACCCACGTTCGCCTTCTCCCCTCCGGCTCTGCCCCGCCAGGCCCAGCAGCTCGGCGCGTGTGGCGGGATCGAGGTCGGCGGTGCCGTGGAACGCAATGGTGTAGCCCGCCGCACGGACCCGCCGGTGCGCCCGGCGCACGCTCTGCATCGCGTGCCCCTCGAGCTTGAAGGTGATGCAGTCGACCACCGCCTCGTCGCCCAGATACACGGGGCGCAGACCGCTGGCCTCGTAGATACCGAGCCAATCTTCTGCGGCCCCCAGAACCGCGACGGACCAGCCCGACCGCTCGGCGTGCGCGGTGAAGTCCGCCCAAGTCTCCCTCGCCTCCTCCGCGGGCCCGATGGGGTCAGGGGAGACGAGGCAGATGCTTCCGCGCACCGAGTGGGCGACGACGCTGCTCCCGGTGAAGAACCACTGCTTGTCGTCCCGCAGCGCGAAGTAGTCCAGCGTCCCACCGCCGTAGCGCAGCACCACCGACCGTGCCCGCTCCCGTTCGCGACGGTGATCTTCCCCCACGAGCGGCTCCGGGACGCGCGGGCTGAACAGCAGCCATGCGACGCTGCCGAGCAGGGCCAAACCCATCGCGGCGAGAACCACGGCCGCGAACCTACCGGTGAAGGGCGGGGGTACGCGTCCAGCCCCGCCCAGATCCCTGAGGACGAGACCGACGAAGTCATCCACCTCGCCCACACCACGGGCCATCTGGGCGAGAACGAGCGAGACCACCACCACCGCGACCGTGCCGCAAACGCCGACCACGACCGCCCGTGCCGCGGCGGCCTGGGAGGGGAGCACGGGGAACGCGCGGCGGCGAAGGCCCAGCCAGATCACGGCCGCGGCCGCCATGGCAGCCTCCTCCACGTCGAGCCCTTTCGTGACATGGAGCATGACCGAGGCAAACAGCAGCAGCTCCGCCACGACCCACGCCAACCGGTGGCCCCGGCGCAGCCCCAGCGCGGTTAGCAGCAGTGCGAAGGACACGAAGACCAGAGTCAGGACCGCTGTCGTGGGCACCACCACGGGCACGACGTCGAGCACCGCGGCGAGCCGCCCGCGCAACGGCCGGGACAGCGCTGACAGCAGCCCCACGGCACCGATCGCCGCCGCGACGTAGGCCGCCCGCCGGCGCGATCGGTCCCGGCGCAACCACGGGTCCGCACCAGCGGGTATTCGACGGGGGGATGGGGCGACAGCGCCCATCACGCCCTCGGGTGGGCGTCGCGACGGATGAGTATGCGGAAGTTCTCCCACGTCATCTCGTAGGCGCCATCAACGAGCAATGCGCGGTGCAGGGGGATGGCGCCCGCTAGGACGACGTAGCAGGGTCCGCTTGTGTTTGTCCTGATGGCCATACCTTCCCGCCAGGCTCGATCCACAACAAAATGCACGCAGCTCGTCAGCTCGTCGAGTCGACCAAGCTCAGAGGTTGCTCAGGGATTGCGGTGCTCAACCAGGTCGTAGATGTCGAACTGAGGCTGTGGCAGCGCGCTGCGCTCGATAGCCTCCTGCACTCGCTGCTCGCCGACCGCAGCGGTCACCGCGTCCGCCGACTCCCAGACGTCGACGACCATCACGCCGTCCGGCGTCTTGGCGAGGGCGTGCCACACCGCTCCTCGTTGCCGCGCAACCTCATTCATCACCGGGGTGAGGTGCTCGAGGACCTTCTCAGCGAGCTCGTCGGGGTTCCCTGTCATCCTCGCGACCACAAGCACGGCCATGGTCATCACCTTCGTCATCGACGCGCCTAGTCCACGCTACGCCTCAGTCCGAAGACGGGGCCGGGTGAGGCCGTGCAGCAGCCTGCTACTTGGCCTCGACCCACTCATGGGTCATTGCCGGAGCGGTACGAGCAATAGGGCCGGCCGCGGTCGTTGGTCAGCGGGGCGGAATGACGTCGTGATCTTGGAGCTCCGGTCTGGCGCGGACGAAGCGGAGTGGGTGGCGGTAGGAGGTGCCGGACCAGGCGACGTCGGCGGTGACCTCGACGACGAGGGGTTCGATGGGGTGACGTCGATGGGTTGTTATGTCCCGGGCCAAGCGGTCGACAGCGCCGCGGGGGATGCGGGTGGGCCAGGGCTGCTCACCGACGGGCGGGTTCGTCCCTTTCATCGCAGCGGTTCGTCGAGCCTGGACAGGCGCAGCAGGTAGCACTGGGGGTAGGTCGGGTCGCACACGACGACCGCGGTGAACGCGACGTCGAACTGGTCGGTGACCTCACGGCCTTCCCATATCCCGGCCCGGTGAAGTCGGACTTCCACCAGCTTGTTCATGCGCGCACGGGGGTCGGCCTGCACGCATCAGTTTCCCACGCCCACGCCGCGCGGGTCCAGGTACGAGGCGCGCCAGGACGCTGCTGATGCTTTGCCCCGATGCGCCGATTCATCGTTCGCCCCCGACGCTGCCCGATCTGCGGCGTGTCCGCGGGCAGTCCGTGCCCGGTCCGAGTCCGGCGACGTGCACCGACGCGCGCGGTGCCCCCGTGCCAGTGGTGTGGCAGCACGGGCCCCGAGCGTGGCAGCGGTGTGGCAGCGACGGACGAGAGTGTTGATCTGTCAGTCAGTACACACACCAAAGGAGAAGCACATGGCTGCGATTGAGAACGTGGTGGTCGTTCGGTTCACTGAGCCGAGCAAGGCCTACCAGGCGCTAAGCGCGCTCAAGGACTGCGACGCCGAGGGTCGGATCGCGCTGCGATCCGCGGCGGTCGTGGAGCGCACCCCTGAGGGATTCCTGCGCACTCCCGAAGCCGCCGACAACATCGGTCTCGTCGGCACTGCGAGCGGCTCGCTGCTCGGGATGCTCATCGGCGTTCTGGGCGGACCGGTCGGAGTCCTCGTGGGCTGGGGCGCCGGTGCCGTGATGGGCGGAGCGTTCGACATCGGTCGTGCCGTGAAGTCGGACGAGGCGCTCACCGAACTGGGCAGGGCGATTCCGCCGGGATCCACGGCGGTGATCGCGACCGCGGCCGAACCGGCGGTCGAGGTGATCGACGGGGAGATGAGGAAGCTGGAGGGCGAGGTCACGCGCCGTCCCGTCGGCGACGTCATGGACGAACTCGAGGCAGCGGAGGATGCCGCCGAGGCGGCTGCCCGCGAAGCGCGGCGCGAGCTGCGCGAGAAGCGGAAGACGGAGCTGAGCGCGAGCGTCGACGCGCGCGTCGGAACGCTCAAGGAGAAGCTCCACATCTCCTGACGGCGATCCGCCGCGCAACGGCGATGTGTTGCGGATGAAGTGATCATCCGGTCAGGACCCGTCGGCCCGAAGGCCGGCGGGTCTCGACGTGCTCGATGATCAGCCGTACCGACGGCGGACGAGTTCGTGCCACGGTTGTGCCACGGATTCGGCCCCTGCCACGGTTCCGCCACGGGCCGATCCAGCGTTTTTGCGCGGGATTGCGCGTCATCGCGAAGGTCTGCGAAACTCATCACCAGAGCCTCGAGATCCGTGGAATCCAGCGGAGTTCTCGGGGCTCGGTGAGATCTATCAGCCGTCTTGGCTGGGTGGGGCGGAAGATTCGCCGACCGGGAGAAGGTCGGGGGTTCGAATCCCCCTAGCTCCACTCCTTGAAGGCCGTTGGTTCGGGTGAAAGCCCAGATCAGCGGCCTTCGGCATTCCCGGGAGTCCTCGATAGGCAGGGCCTGATCATCGACGAGCGGCGCTACTACGACGTCGCGGACCAGCTCGAGCAGCTCGGGCTCAGCGAGTAGCCCGTGCCGGCGCTTCGAGTGCAGTTGGCCGAACTCCGACGATGCTCACATCCACCAGATCGGCGACCTCCAGTCACCCTGGATGGATCAGGACCCCAGTCGTCGATGACCGGAGCCACTTCGTCATCATCGAGTTTGCACACTTCCCTGGCAGGCTCAGCCCACTTCGCCCGTCTGGTTACCGTCCTGCCCCTCGAGGGCTGCCGTGGGTGTGGGGGCGTGGCGGTAAAGCCACGGGCGGCAGACGCTGCTTGGGCCCGCCCCTGTCACGTCATCGCCATGGGCGATGTCATCCGCGTCAGTGGCGCGCACGAGGGGTTGTCCATGGACCCGATGAATGCTCCGATGGGCAGGCTGATGCCGCCGGCGGCTCAGAGTCGGCGTCAAGCGGCTGGAGGAGCACATGGACGTGGATCGCAGCGCGCCGGTCCAGAGGCGTGACGCCCTAGAAATCGACGCGTCGCCGGACGTCGTATGGTCAGTATTGACCGATCTTGAGTCATGGCCGGACTGGATGCCCGGGGTGAGATCGGTCGAAGTAGAAGGTCCATTCGCGGTGGGGATGCAGTTCCGGTGGAAGTCGGGTGGGACTCGCCTCGTCTCTACGGTGATGGACGCCAGCCCCGGGCACTCCGCGGGCTGGCGCGGCAAGACGTTGGGGATTGAGGCGTCGCACGTCTGGCGTCTGCAGAGCCAAGACGGGCGCCGGACGCATGTAGTTACCGAGGAATCGTGGTCCGGAGTGCTGCCGCGCCTGTTCCGGCGCTACGCGGAGAGGATCGTGAGCAAGGCCTTGGCCGAGGGTCTCGCCGCGCTAGGAGCCGAGGCCGCGAGGCGTAAAAGGCCTCCGCATTGAGTTCCTTCTGCAGCTCACGGGGCAGGTATGACAGCAGCTCACGGGGCAGGTATGACAGCCCGACGCAGGGACCCGCTGTCCCCCTGGCTTCCAGGTGTGTCGTCGACGGTCGAAAAGTAGGCCAGGAACGACGGTCGAAGACTAGGCCACCTGACGGCAGGCGGGAGGTGACCACGAAGGGACGGTCAGCCGGCGACGATGGCGCCCAGCCGGGCGACCGCCGCGGCCTCGGCATCGTGGATCGCCGCGACGTGCGCGCTCATGGTCGCGAGGACTGCGGTGAGGCGCTCGTCGTCCAGTGGCGGGGCGTCGTCGTGCGCCGCGCGGAGCTGCCACAGTTCTTCGGCGGCCGCTGCCCGGTCGTCGGCTGTCGCGTCGCCCTCGGCGACCGCTCCCGTGACCGTCGCCGTCAGCTCCCGCAGCCGGGCGATCGCGGGGACGTCGTCCGGCAGGGCGCTCTCGGCGAGGGTATGCCAGCGGTCCGCGATCTCCCGCCACAACGGCGCCTCGGCGGCGAGCGCCGGCTCGTCGAGCACGACGGCGGCCTGCTCGAGCCCGTCGGCGAACAAGTCGCGCAGGTGACCGCCGTCCATCCCGGCGGGCTCGACGGCTTCCCACACATCGGCCAGCGCCCGCAGCAGGCCGCGCCCGTCGGCGAACACCGTCGGCCACCCCTTCTCCGCGCGGGAATCGACGAGCAGTCGAGACCATTTGCGCCAGGCGGGCAGCGCGAAGGACGTCGACGTACCGCCGAGGTGGTCGACGGTGGCCTGCAGCCCAGCGCGCACGGCGGTGCGCAGCTGGTCGGCCGACACCACCGTGTCGGCGGAGCGGACGACGAGCATCGTGTTTTTGTAGCTGCCTACCCGGGCCCGTGCCCGGTCGACGTCGGCCGCCGGCACGGTCAGCGGTGCGAGCGTCCGGTCGTCGACGTGCACGCGGCCACCGGATCGGTCCTCTGAGAGGGCGTAGGCGACGACCGGGTGGCCGCCTGCGCCGTCGAGCAACGCGGGCACGTGCCAGTAGCCCATGTGGTAGCGGTCCGGCCACACGATCGCCGGGTCCCCGCCTGCCAGAGCCGACCTCAGTGCTCTCGCTGCGCCCGCCGCGCCACCGGTGCGCGACCAGGTCACGTCGAGGCCCAATCGGTCGACCGTGGTGGTCAGGCGCCGGTCGAAGTACTGCCACGAGTGCGCGAACCCGAGGGTGACGATGCGGCTGTCGTCGTGGGCGAACTCCCACAGGATGTAGCCGGCCCCGAGACCACCACCGACCACGAAAAGCAGCGGCTCGGTCAACGGCCCGTGCGGTCCGGTGACGCCGCGGTGCGCGAGCACGTTCGTCAGCGCGGCGGTATCCGGGTCGGCGCCGCCACGCAGCGCCCACCCGGCGTCCACGATCGGGTCACCCGCCCCGCCGGCGGGGCGGAGTACGTGAGCCCGGGCGACGGCGTACCGCTCGCCGGTGCGAGCCATCCGCGCGCGCACGCGCGTCTTGAGTTGCTTGGCACTGGTCATGGTCGGATTTCCCGACTGCGCACGCGCCGGCCGGGCCCACGCACCGTCCGCCGCCGCAGCCGTAGTGTCCGGTCGTCCGGGACGTCAGGCCGTGCAACGCCTCGAGGCTCTCGAAGTCCCCTTTGCCCCGCGTCGCCGGCCCGCGTGGAGGACCGGTCTGGGGTTGGGCGTGAGGCACGCCGGGCTCAGTTTACGAGGTCCGAGTCTCGTCCGACAACAGCGACATGGGCATGCTCGGCGGGCCATTGCGTGTGGTGACGAGCGTGCGGACCGATCCCATGCGCGGGTCGAGCCGTTCGCGGGCCTTCGTTAACTTCCTGTGGCGCCCCGGCCAGGCGTCAGGGGGCGAGCCCACCCTGGAGTGCCGGCACAGGACATGCGCGGCTTGTACGAACTGCCGCCGCCACACATCCACGTCTCCCGGCCGTGCAGGTGCGGAGACCTTGGCGACGCGTTGTGCGGTCACGGCTTCAGCAGCCCGGACGGCGAGACCCCCGGATGACGCGAGGAGATCCTGACGCGCAGTACCGCAGGACGGATCAGGAGCTTCAGCGGCGGTTGCAGCGTCACCGCCTCGCCGTCGATCCCCAGGTGGACCGGCTCCGGAGCGTCGATGACCACGGAGCTGGCAGTCCACGCCCGACCGGCCTGATGCCGGGGCCCATCGGGCAGGTCCAGGATCACGATGCCAAGCTGCCCGCCGGCCAGCGTGGGGCGGGTCCCAGTCACGAGCGGGCGGTTCAATGCGTAGGGGTTGTTGGACACGAGCACGACGGCCGGACGCGCGTGCTCGCGACCCCGGTCATCGACGACCTGTACTGCGGGGGCCGCTCCGCTCGGTCCGAGCACCGCCCGAACCGTCTCCGCGAGGGTCCGCACCTTCGCATCGCGGTACTCGGAGCGCTGTATCGCGTCGCCGTAGATCCCCAGCGAGACATTGTTGAGGAACAAGCGCTCGTCGACCTGGCCCACGTCGATCCGGCGCTCGACCCCTTCGGTGAACGCCTCCAGCGCTCCCACGAGGTCGCGCCGATCTACACCGAGATCGAGGGCGAAGTGGTTGCGGGTCCCGGCCGGGATACACACGAAGGCCAGCCCGTGGGAGACCGCCGCTGTCGCCACGACGGCGAGCGAGCCGTCGCCGCCGGCCACGCCTAAGCCGTCGGCGCCCGCGCGCACCGCGTCGGCGACGAGCTCATCGAGGCTAGTTTCCGGGCCGAAGGTGAAGATCTCGATCCCAAGCGCTCGTGCGCGCCCGGCGAGGTCGGCCCGCGCCGCCTTTCCCCCGCCCGAGGTCGGGTTGATGAACAGCACGGGCCGTCGCAACGGGGCGGCCGGAGTCCATCCGTGTCGCAGGGGGCTGGGCCGGGGCAGCTCCGGCGCGCTCATCGGGTCGCTCACAACCAACCGACGCGCCGGAAGTTCCAGTGGAGCGCCCAGACAGCGGCGACCATGACCACCAGCGCGAAGGCGTAGCCAAATGGCCACGTAAGTTCGGGGATGTGATGGAAGTTCATGCCGTAGATCCCGGTGATGATCGTGGGCGCGGCCGCGATCGCGGCCCATGCCGACACCTTTTGCATGATCTCGTTCTGACGGACGGTGACGCGCGACAGGTTCGCACTGAGCAGGCCGTCGAGGCGGCCCGACAGCAGCTCCACCTCCTCGGATAGTCGGCGAGCGTGGTCGCTGGCATCACTCAGGAGGGCGCGCACGCCGTCTGGGGACATCACCGGCTCGCCGCGATGGAGGGTGTCGAACACGGCGAGCACGGGATGCACCGCCCGACCGAGCTGGTCGACGCGGCGGTGGTGGAGGTAGATGGATTCGCTCTGATCGCGATCTCCCTGGAAGACCGCCTGCTCGATCCGCTGAGCCCGATCGAGGAGAAGGTCGGTCACGCGCTCGGCATCGTCGACCACCGTGTCGAGCACGGCCCACACGGCGGCCATCGGGCCGAGCGCCGTGACCGCCGGATACCCGTCGATGCGCCGGCGGATGCTGCCGGAGACGTCGCCGGCCGAGCGGCTGACCACGATGGCGTACCGCGCTCCCACGAAGACGTCGAGCTCGCCGATGTCGAGCTGTCCCGTCGCCTCCTCGTAGCGAACAGTCTTGACGACGATGAAGACGCAGTCACCGTACTGCTCCAGCTTGGGGCGCTGGTGGCCCTCGAGTGCGTCCTTGACGGCGAGCGCTGGCAGGTCGAAGCATCCGCTGAGCTCGTCGAGTTCCCCGCCGGCGGGCTGGCTCACCGCTACCCACACGAACCCCGGCCCTTGGCGGGACAGGCGAGCGGCGTCGGCGATGCTTGTCGCCTCCGCGTCGCGAGCGCCGGCGTGGTACCGCGCGGAGTCAACTAGCAAGGCCGGTCCAGGCTGACCGGCGGCACTCGCGCGCTCAGGCTGCCGGTCGGTGGCAAGGGCTCGACGGGTTTGGTCACCTGCTCGCCTCCCAGGATGCCGCCGAAGGAGCCTGCTCCCGAGCCTTGCTGACGGAGTCAATTGAACACAGGGTAGTGCGCGCGACGACGCAAACAACAGCACGCGCTGCGTGCGGCTGTAGGCACCATCCGGTCTGCCTCTTGTCCGTGCGCACACCGAGCGGGATCGTCTAGATGGTGGATCACGCTCATGCCAGGAGGAGACGACGATGACCCTGACCAGCACGACGGCCCTGACCAGCACGAGCTGCTTCGGGGAGCCGGTGGACGTCGGCAGCGCAGGCTTGGACGCGGTCCGATGACGAGTCCTGCCGGCGCTGACGCATCGGTGCCACGCACGTCAGCCGCGCGTCCCGCCGGGCCGCCGTCGGAGCGCCTCGCCGCGCGCCTGGAGGTGCGCGACGCGACGCCGCCGGCCGTGCTCGACGACCTCACACGGCTCGACCTGGCGGCGTACCGAGCGATCGCCGAGACCCCGACGCCCACGCTCGACGAACCGCTCCGCCGGCTGTCCATCGTCGCGAGCCACTCCAAGCTCTGGATGGGGATCGCCGCGCTCATCGCGGCGTTCGGCGGGCCTTCGGGTCGTCGCACGGCCGTCACGGCGCTGACGGCGGTGGGGGTGAACTCACTCGTCGTCAACCTCCCGCTGAAGCTGCTCGGCCGACGCGCCCGGCCGGACCGTGCGGCAGCACGCGTGTCGCCGACCCGCCATGTCCCGATGCCGACGTCGCCCTCGTTTCCTTCCGGTCACGCGGCGTCCGCGTTCGCCTTCGTCGCTGCGGTGGCGCGGACGATGCCCGGGGTGGCCCGCTACATGAGGGCATTGGCGTACCTCGTCGGCTACTCCCGTGTCCACACCGGCGTCCACTATCCCGGCGATGTCATCGTCGGGGCCTTCATCGGCACGGCGATCGGCGAGTCCGTCGCCTACGCCGCGAGCCCTCGCCCGCGTAGTTGGTTGTAGCGCCGACGGCGGTCCGGGCGACCACGAGCCCGGCAGTCAGTGGATCAGCCTCTCGAGCAGCAGCAGCACGACCCCGAGAGCTCCCTCGACAGCCGCGAACAGGCCTGCGCGCAGCCATGTCGCGCCGGCGCGGCGGCCGGCGACGAATCCCCAGCAGACGATCTGGGCGATCGCTGCGGCCATCGCGAGCGCCGCGCCGGTCTCGCGCGACCACACACCGACCCACGCGAGCGCGAGCGCGAGCGTGGGGACGACCGCCGCTTCGACCAGTGGCCATTCGCGGCGCGCGATGACGAGCGCGTCGCGTCGCCGGAACGTCTCACCTGCCGTAATGCGCGCACCGACGACCTCCGACCACCAGTGCGCGAGCCAGAAGACGAGCATCGATCCGAAGGCGGAGAGCGTCATCTCCCGCGCGTCGCGTCCGGCCTCGAAGGCGAGCCCAACCACGGACGCGACGAGGAAGGATCCGTAAACGGCGGCGCCGAACCGCATGCTCGCACGCGAGCCGAACGGGACGTTCTCGCGGCCGCTGTGCGTCGCTCCCTCGTCGGGGAGGACGCCTCGATCAGAGGCATCCTGCCCGACCCGCTGATCGCCGCGGCGACGAGCACCGCCGTGAGCGCGCTGCTCCCGCGGTCGGTCCAGCGTCTGCATCGAGGCTTCCTGCTCCTCACCCATGGGTGGCCGCCTCCGCCCCGCTCGGGGACCGGAAAAGCTGGTCCAGCTCACCGGCCACGTGCCGAAGCAGGATCGCCAGCGCCACGTCGAACGTGCCGCGGACCAGTGCGAACGCGGCCACGAGCGCCACGAGCGCCATCGCACCGCCGCTGGGCTCGACGAACATCACGACGCCGAACGCGGCGAAAGCGATCCCGCCCACCGCTACCAGCACGGTCCGCGGGCCGCTGAGCGGCAGCACGAACGCCCCGACGAGCTCGATGACGCCAACTGCGATGGCCCAGAGGGCGATCGCGTAGAGGAGCGCCGTTGCCGACAGGTCGGGCCACAGCAGCACCGCTGCTCCGGCCAGGAGCCCGACCACTGCGTGCACGGCCAGCCAGAAGCGGTACCGCTTCGCCGCACCAGGCAGCCCGAACGCGGCCGCGGCAGACACGGACCCGCTCGCGATCGCGAGCACGCCCACCGCCGACACGATGGCCGTGAGGCCGACATCGGGCCAGACGAGCAGGACGATCCCGAACGCGATCGCGACCACGCCCCGCAGGGCGATCAGCTTCCAGACGCGGGCGAAGATCAGCTCGCCGGCCCGGAGCGCCGGGCCAGGGTCGTAGGTTGATTCCATCTTCATGTCCTCCTCCTCAGTCACGCCACGCCGTGGCGGCCTTGGCATTGAGCTCGTCGAGCTCCGCCAGGGCGTGCGTCTTCGCGTCGCGCCAGCCGTCGTCCGTTGCCGTGCCGGCGGCGGCGACGCGCGCGCCGATCGCCAGGCGGCGCTGCCGGAGGTCGGCGATCGCCGCCTCGGCCCGATCCCGCGCAACGCCGGTCTTCGTCGCCGCCTTGGTCTGCATACGGTCTAGGTACGCGTCCCATCGGTGCAGCTCCGCCTCGACTGCGCCTGTGAACTGCTCCTCGGTCGCCGCGAGCTCTGCCGCCATCCGGTGCTCGGCAATCTCGAGCGAGATGTCGAGCTGCTCGAGCCTCCCGGCGACGGCGGCCGCCTCCGTGCGACCCGAGGCCCGCGCGGCCTCCTCGTCGCCGTGCAGGGCGTCGACGTATCGCTGCATCCTGGACCGAGCGTTCGCCGTGCCTTCCTGCGCTCTCACCTCGAGACGGGCGATGCGGCGGCGGACGTCACTCAAGCGTTCCTCTGTTGCTGTGGCCATGGGGGTTCCTTCCTCGTGTTTGCGAACACAAGGGAGCGTGGTCCTCGCCGCTGCCAGACGGCTGCCGCAGACGCAGTCGCGGCTGCCACGCGGGCCCCCGCAGGATCGCCGGCTCAGGCAGGCGCGGTCGCGGCCGTTATCTCGTCGCGGCCGTCGCCCAGACCGGCCAGGCCGACCGCGGCCGCGGCGGCCGGGTCCTGGGACAGCACCACGAAAAGGCTCTCGCGGGGCCCGTGCGCCCGCCGGGCCTTGGACCAGGCGAGCACGGTGCGGTACAGCTTCGCGGCCGTCTTGGCGTCGCCGGCCGCCGCGAGGATGCGACCGAGCTCCACACGCGCATGGGCGGCGGCCCACGACGCACGCGCCGCCTCGGCCGTCGCCAGCGCGCGTCGCTCGAGCTCCTCGGCCTGGGTCACGTCGCCGCCCGCGAGGGCGCTCGACGCGAGCCCGGACAGCGCGAACGCGGCGTGGTCGGCGAAACCTATTCGACCGGCGAGGTCGAGTGTGCGTCGATACGCGACCGTCGCGGCGCTGCTGTCATGCCGCCTCTCGGCGACCCACGCCTCGAGCAGCATCGCGGGAACGAGGAACGCGTCGAAACCCGTGGCCTGGGCGTGACGGCGCGCCTCCGCCGCCATGGCGGCGACCGTGGCCACGTCGCCCGCGGCTGCGGCGACCTGCGCACAGAAGAGGCTGGCCGCTGCGCTCTCCCAGTGGTTCTCGCCGGCGTCGAGCCTCGCATACCCCCGCCCCGCGAGCGCGGCCCCCCGCTCGACGTCGCCTGCCTCGGCGACGGCGAGGCCGAGCGCTGCTTCCACCAGGCCGAGCTCCGGCACCGCCGCCTCGGTGGCTTCGCCCGCGAGGGCCCGTTCGCCGATCTCGATCGCCGTGTCGAGGTCGAGCTCCTCGGTCGCGAGGTAGCAGCGGAAGGCGTGGAGCTCGAGCCGCTCGGCCACCGTCAGATCCCCTGACGTCGCAGCCAGCGCGCGCTCGAGGAAGCGTCGGCCCTCGGCCACGCGTTCGGCAAGGACGAAGTACCAGGCGAGCGCGGCCAAGCGCGCGGCGATGCCGCTCTCGCGGGCATCGCGCGCGTAGGTGAGCGCAGCCCACACGTTGTCGTTCTCGAGCTCGAGCCGGCGGACCCAGGCCCGCCAGTCGGCTCCTCGCAGCTCCGCGCGCGCCGCCTCGGCGAGTGCCGCGATGGACTCGGCGTGCGCCCGCCGGGCAGCGGCGAGACGACCGCTCTCGGCTAGACGTTCGAGCGCGTACTCCCGCACCGTCTCCAGCATGTCGTAGCGCGCACCTTCGGCGGGGAACGACACGGCCAGGATCGACTTGTCGACGAGCACGCCCAGCAGGTAGGTCACGGTGGGCTCATCGAGTCCGTCGCTCGCCGCGGCGGCGACCAGCGACGGCACCGACGCGCCGCCCCGATGTACCGCCACCTTGTGTAACAGCGACTTTTCGTCCTCGTGCAGCACGTCGTAGCACCACTCCACGAGCGCCTGAAGGCTCGCGCGGTTCGCGTCCGATGCCGGCACGTCGCCGAGGAGCTCGAGGCGGTGCTCGACGACGGAGAGGATCTCCACCAGCCCGAGTGCATGGGCGCGCGCGGCGGCAAGCTCGATTGCGAGCGGTAGCCCGTCAACGTGGCGGCTGATCTTCGCCACGAGCGGCGCGGCCTCCGCCGTCAGCTCGAACCCAGGACGAGCCGCCCGTGCGCGCTCGACGAAGAGCTGCACCGCCGGTGAGTCGACGCCGTCGCTCCGGCCCGGATCGGGCACTCTGAACGGCTCGACCATCACCCGCACCTCGCCGGGCACATGCAGCACCTCGCGGCTCGTCGTCAGCACCCGCACGTCCGGACAGCCGGCCACGACCGCTGAGGCGACCCGCGCCGCCTCCCCGACGACACGGCCACAGCCGTCGAGCCACAGGATCGCGTCGGCGTCACGCAAGCGGCCAACGACCCGGGCGAGCGGGTCGGCGCCCCGGACGTCCACGGCGTGCGCGACCAGGCGAACGACGTCGTCCTCCCCGCCGGCACGGGCGAGATCGACGAACCATGCCCCGTCGGCGAACTCATGCTCCACCGAGCGAGCCGCCTCCAACGCGAGCCTGCTCTTGCCGACACCCGGCAGTCCGGTCAGCGTCACCAGGCGGTGCTCGCGCACCAGCGCGAGCACCTGGGCGAGCGCCTCCTCGCGATCGACGAACGAGGTCGACGGAGCGGGGAGGGTGCCTCGGCGCCTCCGTGGAGCCGGAAGGGGCGCGATCGCGGGATCGTGCGAAAGGATGGCGTCCTGGAGGCGCCGCAGCTCGGGTCCCGGCTCTAGCGCCAACTCCTCTGAGAACACGCGCCGCGCCTCACGGAAGGCCTCGAGCGCGTCGGGCTGGCGGCCGCTGCGGTACAGCGCGAGCATCAGCTGGCCCCACAGGCGCTCCCGGAACGGGTTCTCCTCGAGCGCCGTTCCGAGGGCGGGCACGACGTCGCGGTGCTCTCCTAGGACGAGCGCCGCCTCGAACTGCTCCTCGAGTGCGTCGACGCGAAGGGACTCGAGCCGCCGCGCCTCGGCGCCGAACCACGCCGTGTCGGTGAGGCCGTGCAGTGCCGGGCCCCGCCAGAGCTCCAGCCCGCGCGCGACCGACTCCGCCCCCGCGACGGCATCCCCTGCGCGCAGCGCATCACGCGCCTCGTGCAGCAGGTCCTCAAACCGCAGAGCGTCGACCGCCGCGTGGGCCAGCGCGTAGCCGTCCGGCGTCGCGGCGATGGCCTCCGAACCGAGCGCAGCCCGGAGACGGGCGACGTGGTGCTGGACGGCGTTGCGCGGCGCGGCAGGCAGGTCGTCTGCCCACAAGGCGTCGATCAGCGAGTCGACGCCGACGACGCGACCGCACCGGAGCGCGAGCAGCGCGAGAAGCCCGCGGCGCTTGCCGCCGCCTACGTTCGCCGGCTGCCCGCCGGCGAGGACCTCGAACGGGCCGAGCAGTCGGACTTCCACCAGCTTGTTCATGCGCGCACGGGGGTCGGCCTGCACGCATCAGTTTCCCACGCCCACGCCGCGCGGGTCCAGGTACGAGGCGCGCCTGGACGCTAGTGCTGCTTTGCCCCGATGCGCCGATTCATCGTTCGCCCCCGACGCTGCCCGATCTGCGGCGTGTCCGCGGGCAGTCCGTGCCCGGGCCGAGCCTGGCGACGTGCACCGACGCGCGCGGTGCCCCCGTGCCAGTGGTGTGGCAGCACGGGCCCCGAGCGTGGCAGCGGTGTGGCAGCGACGGACGAGAGTGTTGATCTGTCAGTCAGTACACACACCAAAGGAGAAGCACATGGCTGCGATTGAGAACGTGGTGGTCGTTCGGTTCACTGAGCCGAGCAAGGCCTACCAGGCGCTAAGCGCGCTCAAGGACTGCGACGCCGAGGGTCGGATCGCGCTGCGATCCGCGGCGGTCGTGGAGCGCACATCTGAGGGATATCTGCGCACTCCCGAAGCCGCCGACAACATCGGTCTCGTCGGCACTGCGAGCGGCTCGCTGCTCGGGATGCTCATCGGCGTTCTGGGCGGGCCGGTCGGAGTCCTCGTGGGCTGGGGCGCCGGTGCCGTGATGGGCGGAGCTTTCGACATCGGTCGTGCCGTGAAGTCGGACGAGGCGCTCACCGAACTGGGCAGGGCGATTCCGCCGGGATCCACTGCGGTGATCGCGACCGCGGCCGAACCGGCGGTCGAGGTGATCGACGGGGAGATGCGGAAGCTGGAGGGCGAGGTCACGCGCCGTTCCGTCGGCGACGTCATGGACGAGCTCGAGGCAGCGGAGGATGCCGCCGAGGCGGCTGCCCGCGAAGCGCGGCGAGAGCTGCGCGAGAAGCGGAAGACGGAGCTGAGCGCGAGCGTCGACGCGCGCGTCGGAACGCTCAAGGAGAAACTCCACATCTCCTGACGGCGATCCGCCGCGCAACGGCGATGTGTTGCGGATGAAGTGATCATCCGGTCAGGACCCGTCGGCCCGAAGGCCGGCGGGTCTCGACGTGCTCGATGATCACGCGTACCGACGGCGGACGAGTTCGTGCCACGGTTGTGCCACGGATTCGGCCCCTGCCACGGTTCCGCCACGGGTCAAACCAGTAGAATCACGCGCGATTGCGACGGTCTGCGAAACTGAATGCCAAGGCTTTAGATCCGCGGAATCGCGCGGGTTTCGGGCTCGGCCAGACAGTCAGATCAGCCGTCTTGGCGGGTAGGGGAGAGGTCCCGCCGACCGTGAGAAGGTCGGGGTTCGATCCCCCTAGCTCCACCATTGTGATGTCGCAGGACATCCCGGACAGCCCGGACCCACGTTTGTGGATCCGGGCTTTGTGGTTAGCGGGGTTGGTAGTGGCGTGTGAGATCGAGGTGCGCTCGCGCAGGATCTCGCCGGTCGTGGCGTCGTCGATGGTGCTGTGCAGGTCCTGGAGACCATCACGACGGGGGGTGTGTCCGGGATGTCGTGAACCAGCACAGCTCTCGATCCACCGCATGGCCACTGGCCCGCGAGAACGCAGACAGCGGCCATTCGTTTGTCCCGAATTCGTTCGCAATGTGCCGAGCTCCACGGTGGTCAAGTCTCCTCCGTAGAGGAGGAGGATCGCCTAGCCGTCCGGGGCGCCCTGCTCGGCGCAGTGCTAGGCGCGGACCGGTACCAGGGGCGTCATCAGAACCGGTGTGCCCAGCCGGACCTGCCGCAGGTGTCTCGGGCCCGCCGAGCAAGAGGGTGCGGCGCTCCGCGAGGCCCTCCATGCCGAACGGTAGCCGGGGCCCGAACTGACACGCCAGGGTCGGCCAACGGTGGCGCCACTGACTCTGCGCCAGAGCCGGCGCATCTCAGATTGAGGTGGAGCAGCGCAGCGGCGAAAGACAGGTAGCCGAGGGTCACGCCCACATAGCTCGCTACGGGCGTCGGTCGGCCGAACGGCAGAGGCCTTGATCGCCGTCGAGCTGGTGGTCGCCATGAAATGGCGACCGGTGCGGCCCGCTACCAGGCCGTCTCGTCTCTGGCCGCTGTGGTGCCAAGTCAGACGAGGAAGATCGGTAGCGCGCCGGGGTTGTGGGCGTGCACGATCGCGAGGAAGACGAAGACGTCGAAAAGCAGGTGGACGATCAGCACGTACGTGAGGGAGCCGGTCCTCGAGAAGATCCACCCCTGCAGGAGCGCGAACGGGGCGGTGAGGAACGGGCCCCACTCGCGGTAGCCGAGTTCCCACAGGAAAGAGACGAAGATGACGGCTTGAAGCACGTTCGCCTGCCACATCCCGAAGTGTCGGCGCAGCAGCGCGAAGCACGTGCAGATGAAGAACAGCTCGTCCCACGTGCCCACGAAGTTGACCCCCACGAAGAACCGGGCGAGCTCGCTCCGGTCGGTGATGTTCGGCCAGTTCAGGTACGCGCCTGAGGTGATGAAGTAGTACGGCAGGATCAGCCACCCGAGTACCGGGACGGCGACGAGGTAGCCCTTCTCGAGCCGGGTCCACCGCTGGCCGGTGCGCCACGGGAACCGGATGGCCTCGCGGCGGTACACGAACCGGTCCACGAGGTACGGCAGCCCCACGGCGGACAGGAGCACCGTGCCGATCGTGAAGAACCTGTCCCAGCTGACGTCCGCCTCGACCGAGGTCGTCGAGACGATCGTGATGCCGATCCCGACGAGCGCGAGGTCCTTGACTAGCTCGCGCGAGACCGCCCACGCTCCCAGCAGACTGACAACGAGCAGCGCGTGGCCCCAGCCGGCGAGCTGGAGGGCGAACAGGAGGAACGCGGACAGCGAGACCCCCGCCGTCGGCAGCAGCCCGATCAGCGGCGTGTCGTGAACGCGTGGGGCAGCGCTCGTGACCATGCGCGACAGCATGCCAGGCACCGTCGGCAGCGCCCCGGGCGGCGACCGAAGCGCCGGCGGGACCGGCCGGTGCTAATGGTTGCGTGACGAAGCTCGGCTCTCGCGCCGACCCGCGCCGACACCGCGCTGACACCGCGCGCGTCATCAACGCCGCTCAGGGCACCCTGGTCATCGGCAGCAGCAACTATCCCAACGCCACGGAGCATCGACAGCGACGCGCAGGACTGGGAGCTCGAGCTGGCGGCGGTGATCGGAAGCGGACGTTCCGCGTCAGCCCTGACGACGCGCTCGGACACGTCTTCGGCTGCACGATGGTGGACGACATCACCACGCGCGACTCGTCTTCCTCAAGGACATGGCCGCGATCGGCTCGAACCGGTAACGGGCGAAGAAGGGCTCCGGGCTTCCTGCCCGCCGGCATTGGATGCTCGGCGCGCTGGCCGAGCGTCCAACTGTGATATTCACCGGTGACTGTGATATTCACCGGTGAACCGGAGACGCCATAAGCACGGGCGAACGTGAGGGCGACGGCGCGGCCGTTGCCGATGCCTTGCCCTTCTGTCTGACCGCTGCCGACGTCCAGTGCGTGCGGCCTTGGGGCCGGCCGCTCCTGGACGGACGAACTGGTGCATGGTGGGCGCTTGGCGTGAGGCACACCCTGCGCGCAGCCCTACGTGCGCTACACCGGTCAGAGGAGCGCCGCGTCGTTCGTCACGTCGGTGACGCCGACGTGCACGGGAACGTCTCGCAGCTGTTCGGGCGAAAGGCCAAGCACCTGTACCAGCAGTTCGGCGGCGCGGTGCCGAATCATTTCGGCCAGCGGGACCAGCCGGGCGCGGTAGAGGGCGATGATCTCGACAGTGACGGCCTCAAGGTTGTGGTCGGCGTCCGTGGTGCAGGTGATGCGGCTGACGCCGGCCCGGGGGATGGCGTCGAGCGCGTCCCGCAGGTGGGCGACCAGGACGTCGGCCGCGAGGAAGAACTCACCCGCGCCATGGACGCCCCGCACGGGCGCGGAGGGGCGGAACATGGCAAGGGCGTGCGAGAAGACGTCGGCCCGAATGGCCATCCAGCCCCGGTCGGTGTGCTGGCGCAGCGTCGACGCCGCCTTTTCCAGGGGGTTCGTGGTGTTCATCGCCATCCTTCCAGCTTTGTCTCCAGGCTGTGGCGCGCCCGGTGGAGCTGGCCGCGCACGGCGTCGATGGTGGTGTGCCGGATGTCGGCGACGTCGGCGTAGCTCAAACCTTCGATCTCGACCAGGAGCCAGGTCGAGCGCTGGGAGAGTGGGAGTTCTCGCAAAGCCCGGTCGAGGGCGGACAGCAGGTCGGCTGCCAGGGCCTGCTGCTCCGGGTCGAAGCGTCCGGGTGCGGCGATCTGTAGCGAATCCACGGGCAGGGTAGATGGAGGACGGCGGCGCAGGAAGGTCCGCACCTGGTTGATGGTCAGGGCGAAGAGCCAGGTCCGCAGCGCGGCGTCGCCGCGGAAGGCGGGCAGGCCGCGCCAGGCTGCCACCATGACGTCCTGCAGGCAGTCCTGGGTATCGCTGTGGTGCTGGAGCATGCGGTAGCTGTACCGGTACAGCGCCGGACCGTGCCGATCGACGATGACGCCGAAGGCCGCGTGGTCGCGCAGCGCTGCCCGGCGCGCCAGCACGGCGTCGGGCAGGTCGGACAAAGAGGGCACGAACGGTTTGATCACTGGCTTCCCCCGCCGGGTCACACTTCGCGGCCACCAGCCGCCCCGTCGTCACGACTGCGATGAACTACTTCCCCGCCAATGTGATGCACATCACATGCCAGGGATCGTGAGGATCGCCGGACGGCAGCGTCTCACTAGGTGTCACGACGCTGACACCCACGCTGTGTGGCGGCAAGTCGTAGCGACAAGCGAGAGGAGCTCCCGTGAGCGAGCAGTCCGTGGTCCCGTCCGGTGGTGCAATGACCAGCCGTCCTACTGGCGCCACAAACGTCGGCACCGCCACCGTCGTTTCCGCCCTGAGCAGCAGCAAGGGAACCACGACGATCAACGATGTGGTGGTCAGCAAGATCGCCGGCATCGCCACCAATGAGGTCGACGGCGTGCACGCGATGGGCTCGGGTGCGGCCCGCGCGATGGGCTCGTTGCGCGAGCGCATCCCCGGCAGCACCACGAACCAGTCCCGGGGTGTCACGGTGGAGGTCGGAGAGACCCAGGCGGCGATCGACCTCAGCATCGTCGCCCAGTACGGGGTGGCGATCGCTGACCTGGCGGAGGGTATCCGCCGCAACGTGATTGCCTCCGTCGAGCGGATGACCGGCCTGGAGGTGGTCGAGGTCAACATCAACGTCACCGACGTGCACCTGCCTGAGGACGACGTGGCTCCCGAGCAGGAGCAACGGGTCCAATGACCACCGACCGCGAGCCCGCGGCGACTGCCGTATCGACGGGGCAAGAGCTCGCGGACGCGGTGGCCGCGGCGGTCCTCGCCGTCCCGGGGGTGGCCCGCCTGCACTCGGGCGCGCTCGGCGAGGCGGCGACTTACCTGCCCGGTCGCCGCGTGCCCGGGGTGCGCATCCGCCCCGGCGGCGTCGAGGTCCACGTGGTGGTGGACCGGGCGGTGATGGACTGGCGGGTACCCCTTCCCGAGGTGGCCGAGCACGTCCACCGCGCGGTAGCCGCGCTGGTGCCGGCCAGGGTGCACGTCTACATCGACGACTTGGCTACCGAGCCGTCTCCCATGATCCCTTCACCCGATCGTCCCGGCCCGGCCGGAACGATCCGCACCCACCTGGAGTGAGGATGTCCGCTTCCCAGACCGGTCTGCTCGCGGGCCTGCTGCTTGCCCTCGCCGCCATCCTGGGCGGGTTCAACGGCTTCCTGCTCGCGCTCGTCCTCGGTGCGCTGGGCTGGCTGGTCGGCGCCGTGGTCTCCGGCCAGCTCGACCTGTCCGGGCTGCTCGCCGGCCGCGGCCGTGGCTAGCCTCGACACCCGCGACACCCGTGCACGCGGGACGGTGGAGGTCGCGGACCGCGCGATCGAGCGGATCGCCCGCGCGGCGGTCCTGGCCGTCGACGGCGTCGCGCCCGCCGCCAGCACCGCCGGCGGGCTCGGCACCGCCCTGGGCCGCACCTACCCCCGGCTAGACTGTGAGATCGCCGGTGACCACGTGCGCGCCTCGGTCGAGATTGCCATCCGCTGGCCGGCCTCGGCCCGGCAGGTGGGGGAGAAGGTCCAGGCCGCCGTCACCACCCAGTTGCACCACCTGGCCGGTCTGCACGTCGACTCCGTGCGCGTAGTCGTGGCACAGGTCGTGCGCCACGTCGCGGACGAGCCCAGGAGGGTGCGATGACCGCCCACCCGCCCCAGGACGTGTCAACGCCCGGCGCCCGCAAGGCCGCCGCCGGAAGTCTTGTCGACGACCCCGAGCAGGGAAGCTGGTCCAGTCCGGCCGAGCCTGACCGGGAGGCGTGGCGGCCGATGCTCGCGGCCAGCCTGCCCACGCGAAGCGGCGCGATCGGCGTCCTCGGTCCGGTCCTGGCCACCTTGCTCCTGGCCGCCGGCATCGTGCTGGTGATCGAGGCCCTGGTCGCGAGCGGTGTACTCGCCGGCACAGGGCTGGTCGCGACGGGCCTCGCCACGCTCAACGGGCTACCACCCGGTCCATGGTTCCTCGTCGGCGGCATCGTCGCGGCCCTGCTGGGCGTGTGGCTGATCGTCGTCGCCGTCAGCCGCCGGGTCCGCTCCCGGGTCACCGTCACCTCCCGCACCGGGATCTACCTCGGCGTCGGTGACGTCGCCCGCCTGGCCAGCGCGGCCGCCGAGGAGGTCGGCGGCGTCATCTCCGCCTCGACCGTCGCCACCCGCCGCAGGGTCACCACCACCATCCGCTCCACCGGCGACGCGGGCATCGCCGACGCCGTCCGCCAGGCCGTGGCCGACCGGCTCACCATGCTCGACCCTGCCCCACGCATCGTGGTGGCCGTGCGCGGCAAGGGACGTACCACCGACGGGGGGACGCCATGAGCCGCGCAGTGCTCGCCCTCGACCGCACCCTCGCCTTCCTGCTCGGTCTGCTGCTGCTGGCCGTGGGCGCGGCCGCCGTGGCCTGGTGGGCCGGCGAGCTCGACCGCGTGTGGCCCACCGTCCCAGACACCCTCCGCCTGGGCGACGCGTCCTCCGCGGTCGGTGCCCCGTGGTGGCCCTGGGCCGCGGGGGTGGCCGGGGTGCTCGCCATGCTCCTGGGACTGCGGTGGCTGATCGCCCACGTCCCCCGGCGCAACGTCGGCACCCTCGCCCTGCCCGGTACGCCCGGTCGCGGAAGCCTCCGGATCGATCCGGGCGCGGCCGCGACCACCGCTGCCCAGGTCCTGGCGGAAACCCCCGGCGTACGGTCCGTCCGCGGCACCATGCACGACGACCGCGGGGAGCTCGTCGCCGCCCTCAGCGCGACCATCGAGCCCACCGCCGACCTCGCCACCGTCGTCGACCGCGCAGAACGCGTCAGCGCCGAACTGGGCCACGTCCTCGGCATCGACGCCGCCCGCTGCCGGGTGCAGCTCTCCGTCGCCCGCCGCGGCCGGCGCCTACCCCGGGCCGAGTAGCGCTCGACCAGGCTTTCAAGGGGCGACGTGCGCAAGCGACGAATCCGATGAACGCTGGCGAGCCTCTCTTCTGCGTTGTCTGCGTAGGGCTCGGCTCGCCGCGGGAGGCCCTTGACTACGAAATTGTGGGCGCTCACGCTGAGCGGGGCTGCGCGAGTTGGGCCCGACAAGGTGCGGCTAGGGCAACGCGGCGGTGGACTGACGTTCCGACAGGCGGCGCTAGCGTTGCTTGGGTGAGCCTGCCGTGAGGTCGGGGCTGTGGTCGGGTTGGTGGACGCATAGCCATAGTGCTGCGGGTCGGACGATGACCGCGAGGGTGCGGCGTGGGTCGATGACGTCGCCGTCGAGCTGGCAGGGTTGGTTGCGGTCGCTGGTGACGGTGACGCGTGCGCCGCGCAGCACCTCTATCCGGGGCACGTGCTCGTGTCGGCGGAGGATGCCCCAGGCGAGGGCAGCCCAGTGGGCGAGGTGGCGGGGGGCGAGGATGGCGACGTCGAGCTGGCCGTTGTCCGGTTTGGCGTCGGCGAGGAGTTGGACGTCGCCTTGGAGGCGGCCGACGTTGCCGATGACGACGGTGCGTGCGCGCCGGCGGAGCGGTGGGTCGTCGTCGATCTGGATCTGGACGCGCATCGGGCGGTCGCGGAGGTGCTTGAGGGCGGAGAGCACGTAGGCCAGTGAGCCGATGCGCGCCTTCGTCCCCACGCCGACCTTGAGGTGATGGCTGTCGATCGTCGCGCCGTCGTCCCGGAGCTGGACCGGACCTCGAGGTCGTACAGGTAGCCGTCGCCTGGAGCCCAGCGGTGGACGTCGGGCGCAACTGTGCGGCGAGGTCGGGCGACCTCGCCCGCATCGTCGGCCGCGAGCTTGTCAAGTTTTCTGTGTAAGACGGGTTCCGTCCGGTTTTAGTTGATGTGGCCGGCGAGCCGGTCGGGATAGAGATAGAGCAGGGCGAGGTGGTTCAGGGCGGCGTTCCACCCTTCGGTGGTGGCGCCATCGACGAAGTGGCCTTGGCCCTGCGCTTGGAGGCCGGCAGGCCTGCCTCCTTGGCCCGTTCGCGGGCGCGTTTGTCCTCGATGGCGCGGATGGACAGCCAGAGCAGCTTCACCACCGCGTCGTCGTTGGGGAAGTGGCCGCGGTTCTTGATGATCTTGCGCGCCTGGTAGTTCAGCGACTCGATGGTGTTGGTGGTGTAAATGACCTTGCGGACCGCGGGCGGGAAGGCCAGGAACGGGGTGAAACGTTCCCGGGCCCGCTGCCACACCGCGATCGCGGCGGGGTACTTCTTCCCCAGCGGGTGCTCGGCGAGCTCGAGCAGGGCCGTCTCGGCGGCATCGGCGTCCGCGGCGGTGTAGACCCTGCGCAGCCCGGCGGAGAAGGCCTTGCGGTCGCTGTAGGAGACGTACCGGTTCGCGGCCCGGATCAGGTGGACCCACGCAGGTCTGGACCACGGTGCGCGGGAAGGTGGCCTCGATCGCCTCGGGCAGGCCCTCCAGCCCGTCACAGCACGCGATCAGGATGTCCCTCACGCCGCGGTTGGCGAGCTGGGCACACACGGCCGCCCAGAACTTCGCGCCCTCGGCCGCCTGGACCCAGATGCCCAGCACATGCTTGACCCCGTCGGTATCGACCCCGATGACCAGGTGGGCGGCGCGGTTGACCACGTGCCCACCGTCGCGGACCTTGACCACGAGCGCGTCGAGGAAGACCACCGGGTAGACCGGGTCCAGCGGCCGGGACTGCCAGGTGGCGACCTCTTCGAGGACGGCGTCGGTGATGTTCGCGATCGTCTCGTGGGACAGCTCGGTGCCCAGGGTGCGGGCCAGGTGGGCCTGGATGTCACGGATCGTCATCCCGCCGGCGAACAGCGAGATGATCATCTCGTCCAGCCCGCCCAGGCGCCGTTGCCCCTTGGGCACCAGGCGCGGGACGAAGCTGCCGTCCCGGTCCCGCGGGCTCGCGATCGGCACCGGCCCGACCTCGGTCTGGACCGTCTTCGGCATCGAGCCGTTGCGCGAGTTCGGCGTCCCGCGCCCCGCCGGATCGCCCTTGTCGTAGCCGAGGTGATCGCTCAGCTCCACGGCCAGGCCACGCTCCAGGACCGAACGGACCAGCTCGGGCAAAAACCCGCCCTCCCCGGTCAACGGCACCCCGCCGGTGCTGGCCCGGGCCACGAGCCGGTCGATCAGCTCATCGCCGAGCAGCTCCTTACGCAGCTTCCTCGCGGTCGTCTCCGACCCGTCCGAGCCAGGCTGCCCGTCGGCCATACGTTCAGTCTCGGCACCCGCCTCGGCGACGTCCACCGCGTCGAGCTCAGTCCACTGCGTCGTGGTCATGATGGTCTCCTCACGCTGACGTGGCCGTCAGCATCCAGGAACCCCTACTTACACAGACCATCTGACACGCCCGCGCGGCGTCGACGTCATTCTTCACGGGGTAGCTCGCCCCCCAACCAACTAACCGAGCCTCCACCAAACCCGCGGCGGTTCAACCATCTACTCGCTCAACTGGGTCAGAGTGAGGTCATCCCTCCGTCGACGACGAACAGCGACCCCGTCGCATAAGATGACTCGTCGCTCGCCAGGTACTCCATGATCCCTACGACGTCCTCGGGCCTCCCGGCTCGACCGAGCGGCACGCGGGAGACAGCGGCGGCTCGTTTGCTGGTGTCGTTGGCGATGTCCGCCACGAGCGGCGTCATCGTGAATCCTGGGACCACGGTGTTGAACCGGATGCCCGTGCCGGCGTAGTCCGCCGCGGCGACGCGGACCATGCCATGGATGCCTGCCTTCGAGGTGGCGTAGGCGGTGAAGCCGGCGCCCTCTCCGTTGATCGCGGTGGGGCTGCCCGTGACGATGACCGAGGAACCCGGCCGGCGGACGGTGCGGACGGCGTGCTTGAGCGTCAGGAACGTACCGGTGAGGTTGATGTCGATCGTCCGCCGCCAGGACCCGAGCGTCAGCTCACCGATCGGACCGTCGGCCCGGAAGTCCTGGATACCGGCGTTCGCCACCACGACGTCGGGCGGCCCTGCCACGGCCAGCACCTCGGCGAATGCGGCCTCGACCGACTGCTCATCGGCGATGTCCAAAACTACGGGCGACGCGCCCGTCGAGCGTGTTGCGCGTGCCGCCGTGCTCGCGCCTTCGCCGTCGCGGTCCGCAAAGAAGACCACTGCGCCGCTCCGAACAAAGCGAGTCGCCACCGCACGCCCGATCCCGGACGCGGCTCCGGTGACGAGGCACACCTTGCCTTCGAGGACTCTTCCTGGGTGTTCCGTCACGATGCCTCCGATGCTGTCCGTCGTCTCGTCCGATCCGCCTTGCTCGTCGATGCACCCTGGGCGTCCAGCCTGCTCCTCGTCCTTTTACCCCGGTGGTCCGGTCCTCCGCCGTGACCGTCGGCGTAGTAGTGCCGGGAATCCTCCAGGTGCTCGAGCATGGCTGCACGCGCCACCCGGGCGTCACCGCTGCGTATCCCGTCAAGCACCACCTCGTGCTCCTCCGCGGCGACCTCGAGCCGCCCTTCGACCGAGAGGCTGCGGACCCTGATCTGCCGGATGGTGGCATTGATCGAGTCGAGGAGAGTGACGAACAGGGCGTTGTGTGTGGCCGCCGCGACGAGACGGTGAAACTCCTCGTCATGGGTCGCGGCGTCCTCAGGCGTGCGGGACGCCCGCATCGCCTCTAGCTCGACGGCGACCGCGTCGAGATCCTGCGGCTCGGCACGCTCGGCGGCCAGCTCGACGATGGTGAGCTCGAGGACTGCGCGGACCTCGGCGATGTCGGTCGGGGTGAGGAGGTGCTGGGACTGTGCGGACCGGACGTAGAGCTTGAGCGTCTCTGCGACCCGCGAGGACGAGACGGCGGTGACGACGGCGCCCCGGCCGGTTGCTGCCTCGAGCACACCCTTGGCCTGCAGGCTCCGGACTGCCTCACGGATGACCGTTCTGGAGACCCCGAACTGTTCGCTGAGTGCCCGCTCTGTCGGGAGGGCGGTGCCCGGGCGCAGGGCGCCCGACGAGATCGCCTCCAGCAGCTCCTCGCTGACCGTGTGGGCGAGCGACGGTGGGCGCCGGATCGTGTCGAACGAAGTCACAGGGGTCACTTTCTCGCTGCTTCGTTGGGGGAGGAAACACCGGCCATCATACTCGGGGCTTTGGCATACCACCAGACCGTCCGCTATCTCGACTTGCGGGTGACGCCAATGATCATCCCGATCAGTGTCCACATCAAGCGATAATCCGCCCTTGTCAGATGCCAGGACTAGTTCTATGGTCTGGCATACCAAGTGCCGCAACGCGTCCAACTTCCACTGCCAGCCGAGGGGATCAGCGGGTCACAAAGGGACGCGGCACGCAGCGCGGCGGCGGCAAACCGTCGTTCCGGCACGCTGCGTCGCGGCACGACGTCGCAGCAACGAGTCAAGGAGGCCTCGTGTCACTTCTACGCGCGCACCCTGCCCGCAAGCCCGTCCTCGTGGGCGCCATGATGCTCGCCGCAGCGACGGCGCTGGCCGCCTGCGGCACCACCGCCGGCCGTTCCGCCGCAGAGCCCACGGCGCAGGACGTCGCGGTCGACGTCGGCGCCGACCTGACCGGCACGAAGATCTGCTTTGGGTTCTCCGGCAGCGAGACGGAGTTCTGGGCCGCCGGTATCAAGTCGATCAACGACTCTCTGAGCGCGAGCGGAGCCACCGTCATCGAGCACAACTCCAACGAGGATCCCAACAAGCAGCTCGAGCAGGTCCGCGACTGCATCACCCAAGGCGTGGACGGCATCGTCGTCATCCCCGAGGACGGCTCGAGCGCGCTCACCATCATCGGTGAGGCCAACGATGCGGACGTGCCCATCGGCATCTTCAACCGCCCGCCGGCCGACGACACCGGCGCCGCCCTGGTCTCCGTCGCGGACAACCGCGACATCGCGCGCCAGACGGTCGAGTACCTCGCCGCCGAGGCCGAGGGGATCGGTCGCAAGGTTCAGCCGCTCATCATGGTCGGTAACCTCAGCGACCAGAACGCCGTCGAACGGCGGAACGGCTTCTTCGACGCGATCGACGCGAACCCAGACCTCTTCGCGGAGCCGATCGAGGTGCAGACCAATTGGGATGCCGCAACGGGCCAGGCAAATCTCGAGGCCGCCATGCAGGCGAACCCCGACATCGACGTCCTCTTCACGTCCAGCGACTTCCTGTTCCCACAGATCCAGGCCGTGCTGGAGCCGCTCGGCAAGTGGAAGCCGGCGGGCGAGGAGGGCCACGTCATCATGGGTGGCCTCGATGGTGACAACCGCGCCTGCAACCTCATCCGGGACGGCTACGTCGACGCGACCGGCGTGCAAGACCTGTTCCTGGAGGCGGAGTCGCTCCTCGCCGCGCTCGGCAAGGCGATCACCGACGGTCAGACGCAGCCCGACGAGCAGCTCGTCGACGCGGGCTTCGCGCTGACCCAGGCGAACTTTGCCGACCGGGAGCAGGACATGTGGGGCTGCGTCATCACCCCGCCCGGCAGCTGACCTGACCGACCGGCCGCTCTGCGAGCAGCCCTCGCAGAGCGGCCCTGACCCCGGAAGGAGCCACTTTGTCCATCGCCCAGGCCCGCCGGCGCGTGATCGAACGACCGCCCGACAGTCAACGCGTCGACGCGTTCCGCCGGTTCTTCGCCGGGGAGGGGTTCGTCGCCGCGCTCATCGTGGTCTACGTCGTCGTGGTCTCCCAGTTCGCGGACGGGATGCTTACCTCTCGCAACCTGCTCAACGTTCTGAGCAATCTTTGGCCGCTCGCCATCATCGTCATCGGACAGGCGTTCGTCCTGATCCTGGGCGGCATCGACCTGGCCCAGACCGCGGTTGCCAACATCACCAACACGTTCGGGGCGCTGCTGCTCGCCCAGTCCCTTTCCCCCGCGCTGTTCGGCGACACCGTCTTCTGGGGCTCGTTGGTCGGCGAGAGCGGTGGCGTCCTGCGCGACGGCGGCGTCGCCCCGGCGGTCGTCATCGTGCTGGTGCTGGGTCTCGGCCTTGGCGCGCTCAATGGCCTGGCGGTCGCGCGTCTTCACATGCCGCCCTTCATGGTGACGCTGGGCGCCATGCTGCTGCTTGGTGCCGTCGCCGTGTGGATGACCCGCAGCGAGAACGTCGCGTCCCTCCCCGAGGCATATCTCGCCATCGGGAACAAGGGCCTCGGTGGGCCGTTCACGTACGCCATGGTGATCGCGGTCGTAGTCGGGCTGGCCTCGCACTATCTGCTCGCCCGCACTCCCTTCGGGGCGTGGCTCTACGCGGCCGGCACCAACCGGCAGACCTCGATCGTCTCCGGCGTGCCGCACGACCGCACCGTAGTCATCGCATATGCCCTGAGCGGCCTGCTCGCGACTGTCGGCGGCATCCTCTACTCGACGCGGCTCCAGGCCGGCCGCCCCACGCTCGCTGACGACATGCTCCTCGACATCATCGGGGCCGCCGTGATCGGCGGGCTGTCGCTGTTCGGCGGCAAGGGGACGATCCTGGGTGCCTTCCTCGGTGCGGTCTTCTTCGTCGTGCTCTCCAACAGCCTGAACCTCCTCAACCTGCCGTTCACCGTCGTGTTCATCGTCAAGGGCCTCGTCATCGTCGCAGCCGCCCTGCTCGACGTCGCCCGGGCACGTCTCACGGGAGCAGATCGATGACCCCACCACGCCTCGAGCTACGCTCGATCTCCCACAACTTCTTCAATGTCCCGGTCAACAAGGACATCTCCCTGTCCGTGGCTCCGGGCGAGGTGCTCGGGCTCGTCGGTGAGAACGGCGCCGGCAAGTCGACCCTGATGAACGTCGTCGGTGGGGTTATGCAACCGACGGAGGGTGAGCTCTTCGTCGACGGCGAGCCCTACGCGCCCAGCTCGCCGGCCGAGGCAGCCCGGCGCGGCATCGCGCACGTGCACCAGGAACTCAATCTCTTTGCCAACCTCTCCATCGCAGACAACATCTTCCTCACGAACTACCCGCGACGTGCCGGCATCTTCACCGATCGGCGCGCGGCCCGTGAGCGGTCGCGCCGGGCGCTGGACCTCATGGCGCTCCCGTTCTCCCCCGACACCCGGGTCGAGCGGCTCAGCCCCGGCCAGCGGCAGATGCTCGAGATCGCCAAGGCCGCAGTCGGCGAACCGGGCCTGATCATCCTCGACGAGCCGACGACGTCGCTCACCTCTCGGGAGACCGAACGCCTTTTCCAGCTCATCGCCGACCTCACGGCGAGCGGGACGTCCGTCGTTTACGTCTCGCACATCCTCGAGGACGTCAAGGCACTCTCCGACCGGGTCGCGGTGATGCGCGACGGAAACCTCGTCGACGTCCGTGCCGCGTCGGACGCCCCGATCGGCGAGATCATCACGCTCATGGTCGGGCGCAGGTTCGACCAGAGATTCCCCGACCGCGACGGCGCACCCACGTCCGAGCCGGTGCTGACGCTCGACGGCGTGTGCGCGACAGGGCTTGTCGACGACGTCTCGCTGACGGTGCACCGCGGAGAGGTCGTGGGTCTGTTCGGGCTCATGGGCGCTGGGCGCACCGAGCTAGCCCGCATCATCGCAGGGCTCGAGACGGCTGACGCCGGCACGATCACCCTCAACGGCGCCGACGTCGGGTCCACCTCACCGCGTCAACGGATCGCCGCCGGGCTCGCGCTCGTGACCGAGGACCGGCGCGGTGACGGCCTTCTCATGGACTTCCCGGTGATCACGAACGCCGCGCTGCCCTCGCTGGGCCGCTGGAGCCGTCACCCCGTCGCCCCCGTCCAGCGACGCCGGCTCCGACGCGACGTCGCCGCCATCGCGGAGGAGCTGCGGATCAAGACGAGCAGCCTCCGGGAGGCACCGGTGCGCTCACTCTCGGGTGGCAACCAGCAGAAGGTCGTCCTGGCCAAGTGGCTCCTGACGGAGCCCAGCCTGCTCATCCTCGATGAGCCGACCCGCGGCGTCGACGTCGGCGCCCAGTTCGAGGTGTACCGCACAGCCCTCGCCCTGGCCGACCGCGGCGCAGGCATCCTCGCCATCTCCTCGGAGCTTCCCGAGCTCCTCGGCATGTGCGACCGCATCGGCGTCATGCGCCAGGGCCGTCTCGTCGCGGAGTTCGCCAAGGCGGACTTCGACTCCCGGGCCATCCTCGGGGCGGCGTTTGGCGAGGCCCTCGTTCCCGGAAAGGTCGGCTGACCGTGCGATCTGTGCGGAGTCTCGCGCTCAACAACACCCCGGTGCTGCTGCTCGTCGTCGTGTTCCTCGTCTTCTCGGTCGCCGACGCAAGGTTCTTCGACGTCCACACCCTGACCAACGTCGCACGCAGCGCCGCCTATATCGGCATCCTCGCCGTCGGCATGACGCTCGTCCTCATGACCGCGGGCATCGACCTGTCGGTGGGGTCGATGATGTACCTCGTCGCCGTCGTCGTCGGCCAAGTCGCCAACAGCTACGCGCTGCCGGTCTTCCTCGTGCCCGTCCTGGCGATGGCGGTCGGTCTGACGTTCGGGGCGCTCAACGGCTTCGCCATCTCGGTTCTGCGGGTCGTGCCCTTCATCGTGACGCTAGCGATGCTCACCGCGTACCGGGGCCTCGGGCTGGAGCTGTCCGAATCGCGCGAGGTGAACTATCCCGACGTCATCGGGCAGCTGGGCGCCCAGCCGATCCTCGGCGTCCCGTTGCCCGTGTGGGTATTCGTGGTCGTCGTCGTCCTGGCCCACGTGCTCGTCACCCGCACCCCGTTCGGCCGGCAGCTCCTCGCCACCGGGGAGGACCGGCGGGCCGCGGAGCGGGCCGGCATCCCGGTCCGGCGGATCCTCTTCACGGTCTATGTGGTCGCGGGCGCGCTGGCCGGTCTCGCCGCGTTCGTCGCCATGACACAGCTACGCACCGCAGCCCCCGGGTTCGGCACCGCTGACGAGTTCGACGCTATCGCCGCGGCGGTCCTTGGCGGCACCAGCCTCTTCGGCGGCCGGGGCTCCGTGTTTCCTGGCACGGTCGTCGGCGTGCTGCTCATCCAGCTCATCCAGACCGGTCTGCAGTTCATGCAGGTCGACCTCTACATCACCCCGATGGTGCAGGCCGCCATCATCCTCCTCGCCGTGTTCGTCGACAGCGCTCGGACCGGGCGTCTCGAGCGCCTCGGCCGTAGACACATCACCTCGAGCCGGATGGAGACCGCGGCATGACTCCGCCCGACGTGCCGACCGGTCACCACGGCCTCGCACTGACCTTCTACGGCGACGACTTCACCGGCTCAACCGACGTGATGGAGGCGCTCACCCTCGCCGGCATCCCGACCGTCCTCTTCCTCGACGCCCCGACTCCCGAGCTCGTCGCCGTGCACCGAGACGCGCTTGCGGTCGGTGTCGCCGGGATCAGCCGGACGATGTCGCCAGAGGAGATGGACGCAACCCTGCCGGGCATCTTCACCCGACTCGCCGGCCTACGGGCGCCGCTGTTCCACTACAAGATCTGTTCCACGTTCGACTCCTCACCGCACATCGGCAGCATCGGCCGGGCAGCGGAGATCCTCCGGCGGATCTTCCCCGGCTACCCCATGCCACTCCTCGTCGCCGTGCCCCAGCTGGGCCGGTATACCGCGTTCGGCCATCTCTTCGCCACTGCCGGCAGGGACGTGCACCGACTCGACCGGCATCCCGTGATGAGCCGGCACCCGGTGACCCCGATGAGTGAGAGCGACCTCCTGGTCCACCTCGCCGCCCAGACCGACCTGCCGACCGCGCTCGTCGACCTTCGCGCCCTCGGTGGTCCCGACGCCGCCGTCGACGAGCGGGTCGACGCGGTCCTGGCCTCCGGCGCGCAGATCGTCCACTTCGACACGGTCGACGCCGCCACGCAGCGGCAGGTCGGCCGCACGCTGACCCGTCTCGCCGAAGGTCGACCCGACGGCCAACCGCTTGTGGTGATCGGGTCCTCCGGCGTCGAGTACGCGCTCGACCTGGCCTGGCCAGAGGGTCGGCGGGCATCTGTCGGGCAGCCGGACGAGCCCGCCGACGTCGACCAGACGCTCGCGATCGCCGGATCCCGCGCCCGTGAGACGGACGAACAGGTCGCCTTGGCGATCGAGAACGGGTTCGCCGAGGTTCGGGTCGATCCGGCAGCCGCGACCGGCCCCGACGCCGCCGCGTACGCGACCGCCGTCGTCGAGCGTGCGGCGGCCGCGTGGCGCCGAGGCGGCCACGTCCTGGTCCGGACGCCGCCGAAGTCCGGGACGTCCGATGTCGACGGCAACCTGCTCGGCGCCGCACTGGGGCGAATCGCCAGCGAGCTCGGCCTCCTGGTCGACGTGCGACGGCTCGTCGTCGCCGGCGGGGACACCTCGGGCTTCGTCGCTCGCGCGCTGGGTATCGAGACGCTTCGTCTCGTCCGGCAGCTTGCCCCCGGCGCCCCGCTGTGCCGGGCGACGAGCCGGAACGGCCGGTTCGACGGGCTCGAGATCTGCCTCAAGGGCGGGAAGAACGGCACGCCCGACTACTTCGTCCGGATCGCCGCCCTCGCGTCCTCGCGTCTGCTCAACCTCTAAGAAAGGGAACTGACATGACCACGATCGCTCTCATCGGCGCCGGGGGAAAGATGGGCACTCGGCTCGGGGACAACCTCGCCAAGACCGACCACGAGGTCCTCCACGTCGAACCGGGTGAGGCGGGCCGGGCACGGCTCGCCGAGCGGGGCGCCACCGCCGTCCCCGCCGACGAGGCCGTGCCCCGTGCCGACGTCGTCGTCCTCGCGGTGCCGGACAACGCCATCGGGCAGGTCTCCGCCGACCTCATACCGCGGATGAAGGCCGGCGCCACCCTCATCGTGCTCGACGCCGCCGCGCCGTATGCGGGGCAGGTAGCAACACGCGAGGACATCAGCTTCGTCGCGACCCACCCGTGCCACCCGTCGGTGTTCAACCGCGCGGAGACGACGCCGGAGGCGCAGACGGACTACTTCGGCGGCGTTGCGGGACGGCAGGACGTGGTCATCGCGCTGATCTCTGGCACCGACGCCGACTACGAGCGCGCCGAGCAGGTCATCCGCGCGTTCTTCGCCCCGGTCGTCAACGCGCACCGGATCACGGTCGAACACATGGCGCTCCTCGAGCCGGTGCTGGCCGAGACCACGGCCGCCACCTGCATCACGATCATCCGCGAGGCGATGGACGAGGCGGTGCGCCGCGGCGTCCCGGCGGACGCCGCGCGCGCGTTCATCCTCGGTCACATCGGCATCGAGCTCGCCATCATCTTCGGCGAGATCGACTCGCCGTTCTCGGATGGTGCACTCAAGGCCATCGCCGGGGCGCGCAGCATCCTGTTCAAGGACGACTGGAAGCGGGTCTTCGACTCCGACGTCATCGACGCGAGCATCGCCGAGATCGTCGGTGCGCAGTCGCTGACGCACTGAGGGATCAGCTGTGACAGAGCGAGGCGGCCCGCTGAACCTTGTCGCCGGAGCATGGACGGCGACGTTGAACCCGGACGGGGTGCTGGCGGACATCAGGTTCGGCGGCCATCTCGTGCTCAAGGCACTCATGGTCGTCGTCCGTGACGAGGCGTGGGGAACGGTGCCCGGCACGGTGACGGTCGCGCCGCACCACACTGATGACGGCTTCGACGTGCGGCTCGCGGGCGAGCACGTCTACGGGCCGGTGGACTTCGTCTGGGACGGGCACGTGGTCGGCGGGCCGGAGGGCCTGGAGTACCGCTTCGACGGGCGGGCGCGAACCGCGTTCGACTCGAACCGCATCGGTTTCGTCGCGCTGCACCCCCTCGAGCCTGCCGGGCGGCCGGTCGGCGTCTTGCGGGTCGACGACGCCTGGGTCCAGGGCCAAGAGGGTGACGTCGTCGTGACCGAGAGCCGGTTCCCGGCCGACGTCGTCCCACATCAGCCCTTCGTGGGTGTCGCCGGGTTCGTCGAGCACACCCCGCACGGGGACGTCACCATCCGATTCCGGGGTGACACCTTCGAGACCGAGGACCAGCGCAACTGGTCCGACGCGTCGTTCAAGACCTACTCCCGGCCCTTGGCACAGCCCTGTCCGGTGCACTGGCAGGCGGGCGACGAGACCGCCCAGGCGGTCCGGCTCACCGCCGCGGCTCCGGGTGCCTTCTCACCATGGCCCGCCAGCTCGGCTTCGACACAGCCGTACCCAGCCACGGCGACCGTCGTCGTTGACGACGTACCCGCCAGGCTGCCCCACGTGGGGGTGACCGTCGGACCGGAGGACAACCCCGCGCTCCTGGGGGCCGAGATCGCCGCCTTGAGACCGCATCACCTCCGGGTCGACGTTCATGCCGGCCCCGGCGCCCTTCGCGGTGGTGAGGTCCTCACGGCCGCGGGGCGCGCGGGCATCCCGTTGCAGGTCGCGGTCCACGTCGATACCGACCCGGCCCGCGCGCTCGGCGACCTTCGACAACGCCTGGCCGGGGTCGACGTCGCGAGCGTGGCAGTCTTCGACGCCACCGCGCCGTCCACCACCACCCGCGCGATTGACGCCGTTCGCGGTGTCCTCGGCACGGCGCTCGGCGCCGTCTTAATTCTCGTGGGCACGGACGACAACTTCGCCGAGCTCAACCGGAACCGCCTGTCCCTGGACGACTTCGAGGCGTCGGCAGCCGTCTTCAGCCTCAACCCGGGAGTGCACGACATCCGTTCCGCGGCGGTCCTCGAGACAGTCGAGGCGGTGCCCGTCATGCTCGCCACCGCGCGCTCCTTCGTCGGTGGACCGGTCGCTGTCGGGCCGGTGAGCCTACGGCCGCGCCGGAACATCTACCGGGCGGGTGTGGCGATCGACCGGACCGGCCGTGACGACGGCTCGGTGGACGAGCGTCAGCACGCTGCGTTTGCGGCCACTTGGCTGATCGCCACGCTCGCCTCTCTCATCGCCGCCGGTGCACAGGAGGTCACCGTCTTCGAGCTGAGCGGACCGCGCGGACTCGTGGACCGGCCCGGCGGTCGTCGCAGCCCCGCGTTCGAGGTGGTCCGCGCGGTGACCGCCGGCACCGGCGCCCTGACCTGCAAGACCGACGACACTCGCCTGGCTGTGGTGGCGCTCACCTCCCGGCGTGACGGGGACGGGCGTTCCACCACGACGGCGCCGCCGACCACGACCGTTCTGCTGGCCAACCGCTCGACCGACACCGTCGATGTCCGGATCGAGCCAGCCGGCGTCAGCGTCATCCTGCTGCCGCACGGTTACGCCGTCGCCGATCTGCCAGGCGCGCCATCCGCACATCTCGAGGAGCTCCCGTGACCGACCGCATCCGCGCCCGCTACCTCATCGAGACGCCCGCCTCGCCGGCACGCGCCGCAGCGGCCATGGCGGGCGAACAGTCGACCGGCACGTTCATCGCCGTCCCCGGCGAAACACCGGAGATCCATCGCCGGCATGCGGCCCGGGTCGAGGACGTCGTCGAGCTGGACGAGCACGACGAGCCCGCCCTGCCGGGTAGCCGCGGTGGCTCCCCATTTCACCGCGCCGAGGTCGAGCTGTCCTGGCCGCTGGAGAACGTCGGGACTTCCCTGCCCAACCTGCTCGCCACCGTGGCCGGGAACCTGTTCGAGCTTCAGCAGCTCTCCGGCATCCGCCTGGAGGCCCTGGGTCTGCCGGCAGAGCTCAGCCGGGCCCACCCGGGTCCGCAGTTCGCCATCGACGGCACCCGCCGGATCGCGGACGTGTGGGAGCGGCCGATCATCGGCACGATCATCAAGCCCAGTGTGGGGCTCACACCGGAGGAGACCGGTGTGCTCGCCGGTGCACTCTCCCGCGCGGGGCTCGACTTCATCAAGGATGACGAGCTCATGGCGAACTCGCCGCACTCGCCGCTCGAGCCCAGGCTGGCCGCCGTGCTCGCCGCGCTCGACGACGCAGCGTCGGAGACGGGTCGCATGCCTCTCTACGCGGTCAACGTCACCGGCGAGATCGACGAGATGCTCGCCAACGTCGACAGGGTCGCCGAGATGGGCGGCAACTGCGTCATGGTCAGCGTCAACGCGGTCGGGATCGCGGGGCTGCGGGCGGTCCGTCAGCACAGCGCCCTGCCGATCCACGCGCACCGCAATGGCTGGGGGGCCCTGACGCGGGACCCGATGCTCGGGTACTCCTACGACGTCTGGCAGCAGCTGTGGCGTCTCGCCGGGGCCGACCACCTCCACGTCAACGGTTTGCGGAACAAGTTCTGGGAGCCTGACGACTCCGTCCTTGCTTCTGCCAGGGCCGTGCTCGCTCCGATCAACGGCGGGCCGCCCGTGATGCCGGTCTTCTCCTCCGCGCAGAGCGCCGAGCAGGTCGCTGACACCTATCAGGCCTTGGGGTCCACCGACCTCATGTACATCTGCGGCGGCGGGATCCTGGCCCACCCCGACGGCGTGGCCGCTGGCGTCGCGAGCATTCGCCAGGCGTGGGATGCCGCTCTCGGTGGGGTCGACCTGGACGAGCACGCCAGCACCCACCCCGAGCTGGCGACGGCACTCGCCACGTTCCGGAACCGGCATGAACTTTCCTGATGGCAAGGACGCGCCTGCCGTCCTCCTGGGCCATCCCGCGACATCTACCGAGGCGATACCGTCACCATGTACCGGAGGTCTCTCTATGCCATCCACGCACGAGAAGCGTGTGCTCGTCACGGGTGCTAGCGGGTTCATCGCCTCGTGGACCCAGCGCCTGTTGGTCGAACAGGGCCACGACGTCATCGGCACCAGCCGGTACGAGCATCGCCCGGAGTCGCGCTTTGTTCTCGGCCAGTTCGACCCGCCGCTCATCCAGGCCGACAGCCACCACGCGACCGTCCTCCGGAAGGTGGTGAGAACTCACAAGCCGGACGTGGTGATCCACCTCGACGCCTACGTCAACCCGGTCGCGCTCAGGCAAGATCCCCGGCGTGCTATCCGGCAGAACTTCCTGCAGACCGTCGATGTGCTCGACGCCTGCCGCGACTACGGCGTCGCTCGTGTCGTCTTCGCCTCGTCGGTGGCGGTGCTACCGGCAATCCGCTACCAGCCGATCGACGCCGCGCACCCTCTCGTGACGCACACCGAGGGCCCCTCCGGTGGCTTTTACGGGGCCGCGAAGGCGGCGTCGGAGGTATTTGGTCTCACCTACGCCGATTCCTTCGGTCTGGACTTCCGGGTGGTCCGCGCGAGCGCCGTCTTCGGCTTCGGCATGCAATGGCCGATCGGCATCAAACCGCTCGTCGAAGGCGTCGTGCGCGGCGAAGAGGTCACCGTTGCCGTCCACGCGCCACCCCGGGACTACACACCCGTCCAGGATGCCGCGGCGATCTTCGCTGCTGTCGCCGTCGAGGACGACGTTGCCGACCGCGTGTTCTACGCAGCGACGGGCCGGCCCCTGACCGACGGGCATACGTTGCTCGATGCCATGTGGGCGGCGTTTCCGCAAGCGCGCCTACGTGTGAGTGACGAGCCGCTCGATCCCACCGGGATCGAGAGTCGGTACCGCGGGGTCATCGACATCGAGCCCGTGCGGGAGCAGCTCCGGGTGCGGCCAACCTTCTCGAGCCTCGAGGACGCGCTGGTGGCGTACGCGGACCACTACCGCTCGTTCACCTCCGCCCGGAGCGGACCGGCGGAGCGGAAGCTGACTGAGGGGGCCAGGTTCGGGAACTCCAGGTCGTTCAGCCACCTGCTGAACGAGCCACAGATGTGAAGAGATTGACGAGGCCACCATGCGCGTAGCACTGTTCGCGACCTGCCTGAACGATGCGATGTTCCCGCAGGCCGCGGCGGCGACCGTGCGGCTGCTTGAGCGGCTCGGCCACGAGGTTGCCTTCCCAACCGGCCAAGCCTGCTGCGGGCAGATGCATGTCAACACCGGCTACTACGCCCAGGCGCTGCCAGTGATCCGCAACCACGTCGAGACGTTCGCCCCGGTGCTGGACGGCGAGTGGGACGCCATCGTGGCGCCGTCCGGCTCCTGTGTGGGCTCGGCGCGCCACCAGCAGGCCATGGTCGCCGAGCGGGAGGGCGACCGAGTACTGGCCCGGGCCGCGTCGCTGGTGGCGGAGCGGACCTACGAGCTCTCCGAGCTGGTCGTCGATGTTCTCGGCGTCACCGACGTCGGTGCCTGGTTCCCCCACCGGGTCACCTACCACCCCACCTGCCACTCCCTGCGACTACTCAAGGTGGGCGACCGGCCGCTGCGCCTGCTGCGCGCCGTCGCCGGCATCGACCTCGCCGAGCTTCCCGAGGCGGCGTCGTGCTGTGGCTTCGGCGGCACGTTCTCGCTCAAGAACGCCGAGACGTCCACCGCGATGGTCTTCGAGAAGGTCCGCAACGTCGTCGCCACCGGCGCGGAAGTGCTGACTGCGGGCGACTACTCGTGCCTCATGAATATCGCCGGCGCCCTCTCCCGAGCGCGCACGGGCGTGCACGTCGCCCACCTGGCCGAGATCCTCGCCGCCACCCGCGAGGAGCCATGGACTCCGACCGTGCTGCCGGCAGACCGGGCCCGGCAGGGCCCGTCCGGTCACGAGGGCCCACCCGAATGCACGGCGGGAACGACGGCGGCGGTCGGCGACCCCGCGCCGGAGAACCGCCCGGAGGGATCCCAATGAGCGCCACCTTCCTGGGTATGCCGGCGGTGCGGCCGCTTCCGTCCCAGCACCCGGAGAACCCGCTGCGGTGGGGGGCGACGTTCCCCGACGCCGCCCGCGAGACGCTGGGAAACCCGCAGATGCGGGCCAACCTCGGCCACGCCACCCGGACTATCCGGGAGAAGCGGCTGCGAGTGACGGCGGAGCTGCCCGACTGGGAGGCGCTGCGCGACGCCGGCGCGGCCATCAAGGCCGAGGCGATGGCGCGCCTGCCCGAGCTGCTGGTCGAGCTCGAGGAGCAGGTGACCGCGCGGGGCGGGGTGGTGCACTGGGCCCGCGACGCCGCCGAGGCGAACCGGGTCGTCACCGACCTGGTGAGGACGACCGGCGAGACGGAGGTGGTCAAGGTCAAGTCGATGGCCACGCAGGAGATCGGCCTGAACGAGCACCTTGCAGCGCACGGGATCACGGCCACCGAGACCGACCTCGCCGAGCTGATCGTCCAGCTCGCCGGGGACATGCCGTCCCACATCCTCGTCCCGGCAATCCACCGCAACCGCGCGGAGATCCGGCAGATCTTCGCCGAGCACATGGACGACGCGCCGTCGGACCTGACGGACGACCCGCGAGCGTTGGCGATGGCCGCGCGGGCGCACCTGCGGGCAAAGTTCCTCACCGCCAAGGTCGCGGTCTCCGGGGCCAACCTCGCGGTGGCCGAGACCGGCACCGTGGCGGTGTTCGAGTCGGAGGGCAACGGGCGGATGTGCCTCACCCTTCCCGACACCCTCATCACCGTCATGGGCATCGAGAAGGTGCTGCCCCGGTTCCAGGACATCGAGGTCTTCGCCCAGCTGCTGCCGCGCTCGTCCACCGGGGAGCGGATGAACCCGTACACGACCATGTGGTCGGGGATCACCCCCGGGGACGGGCCGCAGCAATTCCACCTGGTGCTCCTGGACAACGGCCGCACCAAGGCGCTCGCCGACGACGTCGGCCGGCAGGCCCTCCACTGCATCCGCTGTTCGGCCTGCCTGAACGTCTGCCCGGTCTACGAGCACGCCGGCGGGCACGCCTACGGGTCGGTCTACCCCGGTCCCATCGGGGCGATCCTCACCCCGCTGCTGCGCGGGACCGGCACCGCACCCGGGCCGCTGGATCTCCATGACCCGACGGCGTCGCTGCCGTTCGCGTCCTCGCTGTGCGGGGCGTGCTTCGAGGCTTGCCCGGTCAAGATCGACATCCCGACCGTGCTCGTCCACCTGCGCAACCGGGTCAACGAGGCTCAGCAGCGGCGGGCGCTGCCCACCGGCTGGCAGGCCGCGATGGGCGCCACCTCGGCCCTGATGGCCTCCGGACGCCGCTTCGGTCCGGCGGCCGCCACCGCCCGGGCCGGTCGGCTGCTCGCCGGGGACGGGCGGATCGGGCACCTGCCCTTCCCGGGCTCGCTGTGGACCGACAGCCGCGACCTGCCCGCCCCGCCGCACGAGACGTTCCGGTCCTGGTGGGCCTCGCACGAGAAGGCCCGCAAGCCCAGAGGGGACGGCGGCGGGGAGAACGGGGGACGTGGCGCGGGGGAGTCATGAGCGACGCCCGCGAGGCCGTCCTGGCCCGCATCCGCGACGCCCTCGGCCGCACGCCGGCCGCCCCGCTGTCGCCCGTGCCGCGCGCGTACCGCTCAAGGTCGGACCTCGCCCCCGGCTCTGTGGAGGCGGTGGACGGGCTCGTTGACCGGCTCGAGGACTACCGCGCCCGGGTGCGCCGGTGCACGGAGGCCGACCTCGCGCCCACCCTCGCCGCCCTGCTCGCCGACGCCGGGTCCGTCGTCGTCCCACCTGCCCTGCCCGCGGCCTGGCTCGCCGGGCTCCCGGGCGGCGCCACGGTGCGCACCGACAGCCCGGACGCCCCGCTGACCAACACCGAGCTCGACGGCGTCGGCGCCGTGCTCACCGGAGCTCGGGTGGCGATCGCCGAGACCGGCACGATCGTCCTCGACGGCGAGCCGGACCAGGGGCGCCGCGTCCTCACGCTGGTGCCGGACCGGCACGTGTGCGTTGTCGCGGCCCAGCAGGTTGTGGCCACCGTGCCCGAGGCGATCGCAATCCTTGGCGCCCACCCCGCCCGACCGCTGACCTGGATCGCGGGCCCCTCTGCCACCAGCGACATCGAGCTACAGCGCGTCGAGGGGGTCCACGGCCCGCGCACCCTTGACGTCGTTATCGTTGGGCTCGAAGGAAGCCGTTGACGACTCCACTGAACAAGTTGCCGGCTGTTCCGGTCCAGAGCGGGAACGCACGTGACCACGGCGGTGGATGACGTGCTCGGCCACGGCGACGTTGATGATCCACGCCGCTACCGTGATCGCCGCCTGGAACGTGGTATTTGGCGGTCTGGCAAGAATCTCGGGTCCGATGATGATGAGAGCCTCGGTGCCGGCGGCTGCGCCAATTGCGTAGGCACGGGTCATCCACGCACTGTGTCGGACGAGGTCGCGACGCCGGACGACGTAGAAGACACCGAGGGCGATGCTCAGCACCATTGATGAGCCGATGATCAGCCGCGGAACAAGCATGATGACACCGCTATGTGCCGGGTGGTTGTAGAGGACCGCCATCCATAGGCCGGAAAGCGCGGCGACCAGCCCGGCGGGCACGAGAACGCGTCCAGCGACCCGGTGCCAGCCCCGGCCACGCAGCGAGGGGACGAACTGGAACGCGCCGAGCAGCGAGTACACGGTGACACTGAGGATGTGAAAGGACAGCGGGAGAGGGGAATCGAAGAACCGCTCGTTCTGCGGTGTGACCTCCGCACCGCCCGCCAGCTCGGTGAGACGCACAGCCCCGCCCAGTATCGGGATGAGGCTGAGCAGTACCAGCCCGGTGGGCACACGCCAGAGCGCAGGTTCGTGCCTCGTTCGACGGCGGGTCGCCTCGGTCGTCATTGGCTGCACGACTGATCCGGGCCGGCGTGGGGAGCGATGGCCATCATCGCCATGTAGCGCCCGCCGCCGTGACGTACCGCCGCCACGTGTATGCCCAGGGGATGACGGCGATGATGACGACGACGAAGGAGCAGTTGAAGAGCACCTCACCGGCCGCGGCGTCCAGGCCGTCGGAGAAGGCGAGGGGGAGGGCGACCGCAGCGAGCCAGATGAGCTTCCATGCCACCTCGAACAGCAGGATCGGCAGCATCGTGACGGGGTACCGAAGGCCGAGCAGCGCCAGGAGCGACATCCCCGTCAGGAGGCAGGCCACGACTCCCTCCATCAGAGGGAGAGAATGGACCCCCTGGACGAACAGCGGCCACTTCACGACAGCCAGCCCCACCCCCATGAACGCGTAGCCGAGGCGCATCACGTTCAGACGGCGAGTGGACAGCCCGCCGTCGCCGGCGCGCTGGGCGGCGGGGAGAGCTGTGTCGCCGGCATTGCCGGCGATCCGGGTAGTGAGCATGACGTTCTCCTCCGGTAGATGACACCGCTGGCCGGATGACCCCGGGGCGGCCGCTGCGTCTGCTGGCTGTTCGTCCACCGGCTTCGGCGTGAAGCGGGAGATCCGAACGCCCGCCCCTTCCGATCTGCTGACCGGTGGGGGCGTTCACGAACGTAGGCGCGCCGGGCGCGGGTGGGATCAGTGGAACGACGGAGCCGGCACTGAACCGGGCACGTCTCAGCTGCTGTGGGCCGCCGCCCAGGCCGCTATCTGGGCCCGCTTGCTGAAGCCGAGCTTGTTCAGCGAGTTCCGCACGTGGCTCTCCACCGTGCGTTCGGAGAGGAAGAGCCGGGCGCCGATCTCCTTGTTGGTGCACCCTTCCGCGACGAGGCGAGCCACCTCCAGCTCACGTCGGCCCAGGGGCGCCGCACCGGTGGCAGCCGACGGGGCGGGCGGGTGAGCCTGCTCTCGTAGGGCGAGCTGGACCGCCGCGGCGCGCCCGAGCGAGCGCCCAACGGTCGTTTCCGCAGCGAACCGAGCCGGCCCGAGCGCCGCTGACGCCGTCGCCATGGCCGGCGTCAGGGCGCGACGGATCCCGGCGTTCAGGGTGGCCCCGGCTTCCTCGCGCAACGTCTCCATGGCGCCGAAGAGCCGGGCGGCCAGCTGCGGCTCGCGGCGCCGTGCGGCGCAGCATCCCAGGCCGCCCAGGAGGTAGCACTGGGCCACCCGGTCGTCGAGGTCCCGGGCGATGGCGAGTGCCTCCAGGAAGTGGTGCTCGGCGTCGGGGGTCCGGCCGAGCTGCAGGGCGCCGATGCCGAGGTTCATCAGCATCATCACCAGGCTGTACTGGTCGCCGAGCTCGCGACTCAGGGCGGCCCCTGGCCTGGCCGAGGCCATGACCGTCGACGGGTCACCGTCGAGGACGCCGTTCAGGGCGGACGCTTGATGCACCATCAGGGTGGCGCCCACCTCGTCGATCCCTGCGGCAATGGCCCTGGCTTCGTCGAGCTGACGGCGGGCAGCGCCCGGGTCTGCCGACATGGTCGAGGCGATGGAGGCCATCGCCAGCAGCCGCGCGAGGAGAGCGGGCGGCCCTTCCCCGCGGGCCGTCGCGATTCCCTCGGACAGGCTGCGGGTGGCCACCGCCGGGTCGTTCTGCAGCACGGCCAGGAAGCCGCGGGCGAAGTGCGCCACCGGGGGGATCTCACCGTCCCTGCCGTCGAGGAGACGGTCGAGACGCCGCGCACCTTCGCTGGTCGCCCGCGTGATCCAGAAGTAGGTCAGGCTGACGGTCAGGTGCACGGCGGCCGGGTCGCCGGCAAGCGTGAGCCGGTCGAGAACGGCGCGGACGTTCTCGGCCTCGAGCTCCATCCAGGACAGCCATGGCAGGAGCCGGCGGCGGCCTTCGGTGGCGAGCTGGCCGCACCTGCGGGAGAAGTGGTCGGCGAGCCGGTTCTGCATGAGGTCCCTCTCGCCGGCGTCGACCAGGCGGAGGTGGCTGAACTCGCGCATGGACTCGTGGAGGCGGTAGCAGGGGCTGGGCGCGGCGAGGTCGCGGACGACGAGCGACTTGTCCACGAGCGAGGACAGCAGGTCGGTGGCCGCAGACGCGGAGTCGGGGTCGAGGCAGACCGCCTCGACGTCGTCGATCTGGAACCGTCCGGCGAAGGCGCTGAGCCGCCGCAGCAGCCGGGCTTCCTGCTCGTCGAGCAGCGCGTAGCTCCACTCGATCGCCGCCTGGAGCGTCTGGTGCCTCGGGAGGGCTGCGGGGGAGCCGCCGGTGAGCAGCGAGAACCGGTACCCGAGCCGCCCACAGATCTGATCGGGTGTCAGGGCCCGGGTCCTGACCGCTGCCAGCTCGATGGCCAGGGGAATCCCGTCCAGCCGGCGGCAGAGCTCGACGACCGACGGCAGGTTGTCATCCGTGAGCGCGAAGTCGCCCGAGGCCGCGGCGGCACGTTCCTCGAAGAGCTGGACGGCTTCGTTCAGACGGACTAGTCCGAGGTTCGCGGTCTCGAGGGACGGCAGGTCCAGGGGCGGCAGCGCAACGACATGCTCCTCGACCAGACCCAACGGCTCTCGGCTGGTGGCCACGATGCGCACCTCGGGCCCGGCCTTGAGCACCTTGCTGGCCAGCTGCGCAGCTGGCTCGGTCAGGTGCTCGCAGTTGTCGAGCACGAGCAAGAGCCGCTTGCCCTTGACATGCGCGCACAAGGTCGCGAGCGGGTCACCGGTGCCATGCTCGCGCAGGTCCAGGGCGGCAAGTGCCGCGCTGGCGACAGACGTGCGGTCACGGACCTCAGCGAGCTCAACGAACCAGACCCCGTCCGGAAAGTTCCGGCTCAGCTGCCCGGCGAGCCGAACGGCCAAGCGAGTCTTGCCCACGCCCCCTGGACCCACCAGAGAGACCAGGCGAGCAGCCTGAAACTTCTTCTTGGCCTCACCCAGCTCCCGTCGGCGCCCGACAAAACTGCTGGTCTCCGCCGGTAGGTTTCCCACCGGCTCGCTCGGCGTCGCCATTCGCCGACAGTATCGCCGGCACCCGAACGGTGCGGGGATCCCCGCACATTCAGTGGTCACTGAGTTATTTGCCGCACCCGCTGCGCAGCCACGGCACATACCGTCCGTAGGATGAATGACGAAGTGATCAGCTCTCGAGTCGAAATCCATCTCACACGAAAGCCACCGGCCGTGCGTGTGGCGCGGGCCGCCGGGGTGAGTGAAGTCAACGTCTGGGGGACGGTCCTCACGTGCCTGGTCTGCGGCAGCTTCCAGCCGCTACTGGAATCGCTGCAGGGATACGAGGTGGTCTGCCTGTGGTCCTCACCCGCAGATTCCTCTCGCAGCCCGAGCATCGGCGAAGACAGGCGCCCGGCCCCGCTCGAATAGGAGCACAAACCGCGTCAGGGGTGCGCGGGTGTCCTAGCCGGCCGGCTGATGCAAGTGGGGCCGGCCTGCGGACCGCTCGTCCGCCCATGACTCGGTGGCCAAGCTCGTCGCCCGGTTGCGCACCACCGGAGCATCAACGTCGAGCAGCCGGTGCTCGTGGTCCGGTAGCCGCGGACATGTGCTGCAAACGGCACCGGTTTCGACAGGATCGGGCCACTTCCCTCAACCGGGGCATCCGTGGCCAGCCGGGAGTGGCAATCAGTCCAACGGGGCAAGCGCTCCACCGCGGAGCACCTCCCCAGACCCTCTTTCGACGCCACCCTCCCGAACCAACCGGGGATGACCATGCAACCCTGGAACCCCGACGACGTGGTGGCCCCACGCCGCCGATGTCCGATCCCCGGTCCGAACGTGCCGTGCGCCGGCACGGCCGCCGCGCGGACCGGCGATGGGGCACCGCATGGAGCCCGGAGCAGATCTCCAACCGGCTCAAAGTCGACTTCCCCGCCGATGAATCGAGCGGATCTCGCACGAGGCGATCTACCAGGCCCTGTACCGCCAGGGCCGCGGCGGGCTGCGTCGGGAGCTGACGGCGTGCCTGCGCACCGGGCGAGCGCTCCGGACGAGCGCTCCGGGTACCGCAGGCGCGCACCCGTCGTCGCGGAAAGCACTTCGTCACCGAGGAAGTGATGATCAGTCAGCGGCCTGCCGAGGTCACCGACCGGGCCGTCCCTGGGCACTGGGAGGGTGCCTGATGATCGGGCTGAACGCCTCGGCCATCGGCACGCTCGCGGAGCGCAGCACGCGGTTCACGATGCTGCTGCACCTGCCACGAATGGCAGAGTTCGCCTTCACGGACCGGGTCAAGAACGAGCTACCGCTGGCCGGCCACGGCGCCGAGGCCGTCCGCTACGCCATCGTCGAGCAGCTCGGCGCGCTGCCCGAACAGTTGCGCCGGTCGCTGACCTGGGACCAAGGAGCGGAGAGATAGCTCAACACGCCCTTCTGCGCATCGACCTCGACCTGGCCGTCTACTTCTGCGATCCCCACTCACCCTGGCAGCGCGGAACGAACGAGAACACCAACGGCCTGCTGCGCGAGTACTTCCCCAATGTCACCGACCTCACCAGACACACACCCGGCGACCTGCAGGCCATCGCAGCGGCCCTCAACTCCCGACCCCGCAAGATCCTCCAGAGGAGAACACCCGCCGAAATCATGGACGAGCACCTACGATCAGGCGGTCAAGCCGGTGTTGCATCGACCCGTTGAACCTCAGCAGCGAGCCGGCATCGGAGTGGTGGATCAGCCCGGCGTTGATGGGGTGGCCGTCGCGGTCGCGGCGCCAGGTGGCCGTCGTCACGGCCGTGAGGACCAGGTCGGTGTGCTTGGTCGTCATTGCGTGCCAACCCACGATCGCCTGGGAGAAGAGATCCACGGCGAAGGTGACGTAGACAAACCCCGCCCAGGTGCGCACGTAGGTGAAGTCGGCCACCCAGGCCAGGTTCGGGGCCGGGGCGGTGAAGTCCCGGTTGAGCTTGTCCCCGGCCCGCTTCTGTCCTTGCCGGCACCGTGGTGCGGACCTTGCCGGACCGGATGACCCCGTGCTTGCCGTGCTCACGCATCAGCCGCTCGACGGTGCACCGGGTCACCGCGACGCCCTTGGCGCACAGGGCGTGCCAGGTTTGCGGTACCCGTACAGGCTCTCCGCCGTGGCCTTGCCGGCCACATCGAGACGCAGCGAGCGGATCTCGTTGAGGACCACCGCGTCGGTCACTGTGCGCTTCGCCGGCTTCGCCGGCTTGCGGGAGCGGTGGGCGTAGTGGGTGCTCGGGGCGATCTTGCACCCGTGCTCGGTCAGCACGGTGCAGACCGGCTCGACCCCGAACCGGTCCTTGTTCTCGTCGATGAACCGGCAGACCAGCGGCGTGGCGGGTCGGGCTCCCGCGCGAAGAAAGACGCTGCTGCCTTCAAGATCTCATTCGCTCGCCGCAGTTCCTTGACCTCGCGCTCGAGCTCCTTCACGCGCGCGTATTCCTCACTGGTCACGCCCGGCCGCTTGCCGGTATCAACCTCACTCTTTCGCACCCACAGGCGCAGGCTCTCGGCGCCGATGTCGAGTTTGGCTGCCACCGCTTTGATCGCGGCGTACTGCGAGGCGTAGTCGCTCTGGTGATCCAGCACCATCCGGACCGCGCGGTCTTTCAAATCGTCGGGGCAACGCTTCGTTGACAC

Protein sequences of DBSCAN-SWA_1

>NZ_CP040915|725198:791602|769782_770601_-|WP_168205572.1|DBSCAN-SWA
MTSFDTIRRPPSLAHTVSEELLEAISSGALRPGTALPTERALSEQFGVSRTVIREAVRSLQAKGVLEAATGRGAVVTAVSSSRVAETLKLYVRSAQSQHLLTPTDIAEVRAVLELTIVELAAERAEPQDLDAVAVELEAMRASRTPEDAATHDEEFHRLVAAATHNALFVTLLDSINATIRQIRVRSLSVEGRLEVAAEEHEVVLDGIRSGDARVARAAMLEHLEDSRHYYADGHGGGPDHRGKRTRSRLDAQGASTSKADRTRRRTASEAS
>NZ_CP040915|725198:791602|727425_727782_+|WP_139927230.1|DBSCAN-SWA
MPDDVRAALDERRDLIEARAQALAESAVRHRAPWVLRIGEPPLDGTERARWVRQLAVVAAYRDRYGVTSQDPLGPEAETLAQRRDAERAAAALRGARAIADTNTPRGMSPLSAGRKIG
>NZ_CP040915|725198:791602|790583_790988_-|WP_139927281.1|integrase,transposase|DBSCAN-SWA
MSTASTGSSGPARSAPRCRQGQKRAGDKLNRDFTAPAPNLAWVADFTYVRTWAGFVYVTFAVDLFSQAIVGWHAMTTKHTDLVLTAVTTATWRRDRDGHPINAGLIHHSDAGSLLRFNGSMQHRLDRLIVGARP
>NZ_CP040915|725198:791602|764876_765254_+|WP_168205571.1|DBSCAN-SWA
MASLDTRDTRARGTVEVADRAIERIARAAVLAVDGVAPAASTAGGLGTALGRTYPRLDCEIAGDHVRASVEIAIRWPASARQVGEKVQAAVTTQLHHLAGLHVDSVRVVVAQVVRHVADEPRRVR
>NZ_CP040915|725198:791602|754250_754895_-|WP_139927251.1|DBSCAN-SWA
MGEEQEASMQTLDRPREQRAHGGARRRGDQRVGQDASDRGVLPDEGATHSGRENVPFGSRASMRFGAAVYGSFLVASVVGLAFEAGRDAREMTLSAFGSMLVFWLAHWWSEVVGARITAGETFRRRDALVIARREWPLVEAAVVPTLALALAWVGVWSRETGAALAMAAAIAQIVCWGFVAGRRAGATWLRAGLFAAVEGALGVVLLLLERLIH
>NZ_CP040915|725198:791602|725198_726554_+|WP_139927229.1|integrase|DBSCAN-SWA
MAHDKLGPGEHGEIFIKRHKSGKFQARVRVRLFNGEETQVSRNRKTGAAARLAVQAEIDTLLNAPRGSAQLKPDSRVGLAARQWIDDLRLQSTWPNPPRRPQTVDEYERLLGTQLIPKLSKYRLNELTTAVCQDWVNSIIEAGKSGPYDMVVTAAQARGAFKAVIDRAIVHDALRYNPMDKTTTPKRKVPDPKAMTVTDVYRLRKAVRDWECARVGRPGPPPTGHVPAAIDVMLGTGLRIGEVLALNWGKVNLSRDGLPTIAVDATLVDIKGHGTVRQEMPKTDAGKRTIIIPKFTVESLEAIRPPITRPDMPLFPSRRFRDGRASLKPQTPHNVRRTLRAALEFANMTGEVHPHLLRSTVATFVARERGMADAAALLGHKVNGGVTVRHYIERLRLAPDASTVLQAMVEIGEEEAAKATHQRTTGADAARADAPAVTAAKVAVAGEDSGW
>NZ_CP040915|725198:791602|781090_782164_+|WP_168205574.1|DBSCAN-SWA
MPSTHEKRVLVTGASGFIASWTQRLLVEQGHDVIGTSRYEHRPESRFVLGQFDPPLIQADSHHATVLRKVVRTHKPDVVIHLDAYVNPVALRQDPRRAIRQNFLQTVDVLDACRDYGVARVVFASSVAVLPAIRYQPIDAAHPLVTHTEGPSGGFYGAAKAASEVFGLTYADSFGLDFRVVRASAVFGFGMQWPIGIKPLVEGVVRGEEVTVAVHAPPRDYTPVQDAAAIFAAVAVEDDVADRVFYAATGRPLTDGHTLLDAMWAAFPQARLRVSDEPLDPTGIESRYRGVIDIEPVREQLRVRPTFSSLEDALVAYADHYRSFTSARSGPAERKLTEGARFGNSRSFSHLLNEPQM
>NZ_CP040915|725198:791602|785217_785988_-|WP_139927278.1|DBSCAN-SWA
MTTEATRRRTRHEPALWRVPTGLVLLSLIPILGGAVRLTELAGGAEVTPQNERFFDSPLPLSFHILSVTVYSLLGAFQFVPSLRGRGWHRVAGRVLVPAGLVAALSGLWMAVLYNHPAHSGVIMLVPRLIIGSSMVLSIALGVFYVVRRRDLVRHSAWMTRAYAIGAAAGTEALIIIGPEILARPPNTTFQAAITVAAWIINVAVAEHVIHRRGHVRSRSGPEQPATCSVESSTASFEPNDNDVKGARAVDPLDAL
>NZ_CP040915|725198:791602|736432_737038_-|WP_168205559.1|DBSCAN-SWA
MLAHLGKVPLVVVMAAAVLGAVVGDNIGYAVGARLEPKLDARAPDRARRHLAAAEAVVQRWGAPAVLIGRWAALLRAVVPCVAGASGLPYRRFVVFNVLGGALWGVAVAGIGYLAALRPGRAEPRTGRDDPRAPGPARSHGRGTPHGPTPDAMVTCGRTAIRTGRRGRPCFSRGSHPPRRTLAPSGQLAAQSRWSRNHDRD
>NZ_CP040915|725198:791602|727989_728178_+|WP_139927231.1|DBSCAN-SWA
MRPRVAEYLGVPVRTIYDWRQSGHGARGIRVGRHLKFAVSDVAAWIDAQREATQDGRDRAKG
>NZ_CP040915|725198:791602|782183_783071_+|WP_139927275.1|DBSCAN-SWA
MRVALFATCLNDAMFPQAAAATVRLLERLGHEVAFPTGQACCGQMHVNTGYYAQALPVIRNHVETFAPVLDGEWDAIVAPSGSCVGSARHQQAMVAEREGDRVLARAASLVAERTYELSELVVDVLGVTDVGAWFPHRVTYHPTCHSLRLLKVGDRPLRLLRAVAGIDLAELPEAASCCGFGGTFSLKNAETSTAMVFEKVRNVVATGAEVLTAGDYSCLMNIAGALSRARTGVHVAHLAEILAATREEPWTPTVLPADRARQGPSGHEGPPECTAGTTAAVGDPAPENRPEGSQ
>NZ_CP040915|725198:791602|739570_740902_+|WP_139927239.1|DBSCAN-SWA
MPHSLGARVTLVFAVGAAAALVLCLALLYLILSRQLVTALDDDLRARSADLVAAVAAGDVEVVVRDPLAQLYGPEGAVIAGSAALGDSRLLSPDGVHRVRAEELRTRLLARGEEAPTAVRVLSQRVGGDGVLSVAVSVEPLHEARRRLLEVLVLAAPLLVAVLAVAGWLVVRAALRPVDVLTREAAAISTFEAARGLPPVPGDDEIARLARTLDAMLRRLRVAFERERAFVDDASHELRTPIAVVLGELELALSAVDDPEEVERSLRAALGEAQRLSRLAEDLLLLARAQAGSLVIRREPADLLDLAVTEAGRLAPVLGARIQVSGEPATVVGDPDRLRQVLTNLARNSAAAGATTVRVRVARDQARAILEVADDGPGFPPGARDQAFERFVRGTGPRTPGGSGAGLGLSIVRAIVTAHGGTVEARNGDPLGGAVVTARLPLA
>NZ_CP040915|725198:791602|740972_741905_-|WP_139927240.1|protease|DBSCAN-SWA
MNALAHRTSTTPASWPRLGWLAVLVTGLVLFGAVGAVTLDTGDPIFLPCLLLLGAAIVPVTLTTFVTAVAHTHLSLPNILTAAVLGGVLGGILAGTLEFDAARTLGWLPFAIVALIEECAKLAVPAVFLAWLAWRHTRPRAVDGLVLGVAVGSAFAAVETMGYAFTVLLRTGGNLQPVDHLLALRGLGSLGGHAAWTGLACAALFAVPDARRRGLASLRFLAVLVAAICLHAGWDSAAAIGHGDLAIGLLSFTALMALTWWLHRAARRSAESPKAANRPPTGWIRPGAAPGGPPSTSGTLAGAPVTSAGP
>NZ_CP040915|725198:791602|741901_743899_-|WP_139927241.1|protease|DBSCAN-SWA
MPTFQAPSSQQRTDRPTARSGTGHDRRPGPGGSPRWQPMWPRWALPFGVVLLLLLSFGPGLLGSQGTEHLSYSTFLSDVRHHDVSSVAVGSQGQVTGVLTSGKDFVTQAPVWALTTTDLSHQLEQAGVHVSAFQQGGSLFQQGGSLAQVVASFLPMLLLIGAMVWMGRRGLASTFRTKAKVSDAERPHTTFDDVAGYDGAKEEVREVVDFLQHPDRYLETGARGPRGVLLVGPPGTGKTLLARAVAGEANVPFYAATGSSFVEIFAGLGASRVRDLFAQARASAPAIVFIDEIDAIGGRRGVAGIAGNDEREQTLNQLLAEMDGFTQNTSVVVLANTNRPEILDPALLRPGRFDRQVTVPLPALADRERILAVHTRDKHLSADVDLHALARGTPGFSGADLANLVNEAALRAARANRRTIRAADFDAARDRLILGRPETSALLPDERRRVAVHESGHAVVAALSPTADPVAKITILPAGTALGATHQLPVDERRLYSEQYLTDLLTVRLAGRAAELVVLGQASTGAADDLAGATQLAQRMVLEYGLSRLGPVAYPPSPTSRLDGGPDRPYADDTQRRVDAEVTRLLNEADERAAALLAGHRSALDKVTHLLLETETVDGAIVYDILHRVATGSPEGPVPSGFAAWLADPSSDTHPFRDTTSRRIQ
>NZ_CP040915|725198:791602|764704_764884_+|WP_139927260.1|DBSCAN-SWA
MSASQTGLLAGLLLALAAILGGFNGFLLALVLGALGWLVGAVVSGQLDLSGLLAGRGRG
>NZ_CP040915|725198:791602|752201_753170_-|WP_168205566.1|DBSCAN-SWA
MLVDSARYHAGARDAEATSIADAARLSRQGPGFVWVAVSQPAGGELDELSGCFDLPALAVKDALEGHQRPKLEQYGDCVFIVVKTVRYEEATGQLDIGELDVFVGARYAIVVSRSAGDVSGSIRRRIDGYPAVTALGPMAAVWAVLDTVVDDAERVTDLLLDRAQRIEQAVFQGDRDQSESIYLHHRRVDQLGRAVHPVLAVFDTLHRGEPVMSPDGVRALLSDASDHARRLSEEVELLSGRLDGLLSANLSRVTVRQNEIMQKVSAWAAIAAAPTIITGIYGMNFHHIPELTWPFGYAFALVVMVAAVWALHWNFRRVGWL
>NZ_CP040915|725198:791602|751266_752118_-|WP_168205565.1|DBSCAN-SWA
MLFINPTSGGGKAARADLAGRARALGIEIFTFGPETSLDELVADAVRAGADGLGVAGGDGSLAVVATAAVSHGLAFVCIPAGTRNHFALDLGVDRRDLVGALEAFTEGVERRIDVGQVDERLFLNNVSLGIYGDAIQRSEYRDAKVRTLAETVRAVLGPSGAAPAVQVVDDRGREHARPAVVLVSNNPYALNRPLVTGTRPTLAGGQLGIVILDLPDGPRHQAGRAWTASSVVIDAPEPVHLGIDGEAVTLQPPLKLLIRPAVLRVRISSRHPGVSPSGLLKP
>NZ_CP040915|725198:791602|764309_764702_+|WP_139927259.1|DBSCAN-SWA
MTTDREPAATAVSTGQELADAVAAAVLAVPGVARLHSGALGEAATYLPGRRVPGVRIRPGGVEVHVVVDRAVMDWRVPLPEVAEHVHRAVAALVPARVHVYIDDLATEPSPMIPSPDRPGPAGTIRTHLE
>NZ_CP040915|725198:791602|746829_746994_-|WP_168205562.1|DBSCAN-SWA
MNKLVEVRLHRAGIWEGREVTDQFDVAFTAVVVCDPTYPQCYLLRLSRLDEPLR
>NZ_CP040915|725198:791602|786715_788998_-|WP_139927280.1|DBSCAN-SWA
MATPSEPVGNLPAETSSFVGRRRELGEAKKKFQAARLVSLVGPGGVGKTRLAVRLAGQLSRNFPDGVWFVELAEVRDRTSVASAALAALDLREHGTGDPLATLCAHVKGKRLLLVLDNCEHLTEPAAQLASKVLKAGPEVRIVATSREPLGLVEEHVVALPPLDLPSLETANLGLVRLNEAVQLFEERAAAASGDFALTDDNLPSVVELCRRLDGIPLAIELAAVRTRALTPDQICGRLGYRFSLLTGGSPAALPRHQTLQAAIEWSYALLDEQEARLLRRLSAFAGRFQIDDVEAVCLDPDSASAATDLLSSLVDKSLVVRDLAAPSPCYRLHESMREFSHLRLVDAGERDLMQNRLADHFSRRCGQLATEGRRRLLPWLSWMELEAENVRAVLDRLTLAGDPAAVHLTVSLTYFWITRATSEGARRLDRLLDGRDGEIPPVAHFARGFLAVLQNDPAVATRSLSEGIATARGEGPPALLARLLAMASIASTMSADPGAARRQLDEARAIAAGIDEVGATLMVHQASALNGVLDGDPSTVMASARPGAALSRELGDQYSLVMMLMNLGIGALQLGRTPDAEHHFLEALAIARDLDDRVAQCYLLGGLGCCAARRREPQLAARLFGAMETLREEAGATLNAGIRRALTPAMATASAALGPARFAAETTVGRSLGRAAAVQLALREQAHPPAPSAATGAAPLGRRELEVARLVAEGCTNKEIGARLFLSERTVESHVRNSLNKLGFSKRAQIAAWAAAHSS
>NZ_CP040915|725198:791602|777054_777903_+|WP_139927271.1|DBSCAN-SWA
MTTIALIGAGGKMGTRLGDNLAKTDHEVLHVEPGEAGRARLAERGATAVPADEAVPRADVVVLAVPDNAIGQVSADLIPRMKAGATLIVLDAAAPYAGQVATREDISFVATHPCHPSVFNRAETTPEAQTDYFGGVAGRQDVVIALISGTDADYERAEQVIRAFFAPVVNAHRITVEHMALLEPVLAETTAATCITIIREAMDEAVRRGVPADAARAFILGHIGIELAIIFGEIDSPFSDGALKAIAGARSILFKDDWKRVFDSDVIDASIAEIVGAQSLTH
>NZ_CP040915|725198:791602|791015_791231_-|WP_139927282.1|DBSCAN-SWA
MLTEHGCKIAPSTHYAHRSRKPAKPAKRTVTDAVVLNEIRSLRLDVAGKATAESLYGYRKPGTPCAPRASR
>NZ_CP040915|725198:791602|759388_759997_+|WP_168205569.1|DBSCAN-SWA
MAAIENVVVVRFTEPSKAYQALSALKDCDAEGRIALRSAAVVERTSEGYLRTPEAADNIGLVGTASGSLLGMLIGVLGGPVGVLVGWGAGAVMGGAFDIGRAVKSDEALTELGRAIPPGSTAVIATAAEPAVEVIDGEMRKLEGEVTRRSVGDVMDELEAAEDAAEAAAREARRELREKRKTELSASVDARVGTLKEKLHIS
>NZ_CP040915|725198:791602|737408_738065_-|WP_139927237.1|DBSCAN-SWA
MSGGDVHRGRRTEGESRWGAAAAVAAAAGLHLALPDRLTSGPRWIVPALEVALLVGLLLANPTRLTRESRDARALSLALVGVIAAANAVSLVAITRLLLAGGRANGRELIVAAVGVWLTNVVVFALVLWEIDQGGPHARSVGRDRPPELLFPQMSMGQTDWTPTFADYLYISFTNSTAFSPTDTLPLSRRVKMAMLAQELLSFVTVGLVVARAVNILA
>NZ_CP040915|725198:791602|786031_786499_-|WP_139927279.1|DBSCAN-SWA
MLTTRIAGNAGDTALPAAQRAGDGGLSTRRLNVMRLGYAFMGVGLAVVKWPLFVQGVHSLPLMEGVVACLLTGMSLLALLGLRYPVTMLPILLFEVAWKLIWLAAVALPLAFSDGLDAAAGEVLFNCSFVVVIIAVIPWAYTWRRYVTAAGATWR
>NZ_CP040915|725198:791602|738764_739283_-|WP_139927238.1|DBSCAN-SWA
MGSLRHRHGWELHPAVRAERRSAGERAIERAGDVLGSWVLVASLPILVALGIAVAVWHDRAQGPVALLTLGLSGLMVCDLQLVLLQARRANRMAAQVALYDLEWDRRRAAAVDELRDDMGRLHADLARLSALVETTRTPQATRGDGGRRDVETERSEEHVGPPSSGGGRGRT
>NZ_CP040915|725198:791602|770993_772019_+|WP_139931301.1|DBSCAN-SWA
MLAAATALAACGTTAGRSAAEPTAQDVAVDVGADLTGTKICFGFSGSETEFWAAGIKSINDSLSASGATVIEHNSNEDPNKQLEQVRDCITQGVDGIVVIPEDGSSALTIIGEANDADVPIGIFNRPPADDTGAALVSVADNRDIARQTVEYLAAEAEGIGRKVQPLIMVGNLSDQNAVERRNGFFDAIDANPDLFAEPIEVQTNWDAATGQANLEAAMQANPDIDVLFTSSDFLFPQIQAVLEPLGKWKPAGEEGHVIMGGLDGDNRACNLIRDGYVDATGVQDLFLEAESLLAALGKAITDGQTQPDEQLVDAGFALTQANFADREQDMWGCVITPPGS
>NZ_CP040915|725198:791602|783001_784633_+|WP_168205575.1|DBSCAN-SWA
MHGGNDGGGRRPRAGEPPGGIPMSATFLGMPAVRPLPSQHPENPLRWGATFPDAARETLGNPQMRANLGHATRTIREKRLRVTAELPDWEALRDAGAAIKAEAMARLPELLVELEEQVTARGGVVHWARDAAEANRVVTDLVRTTGETEVVKVKSMATQEIGLNEHLAAHGITATETDLAELIVQLAGDMPSHILVPAIHRNRAEIRQIFAEHMDDAPSDLTDDPRALAMAARAHLRAKFLTAKVAVSGANLAVAETGTVAVFESEGNGRMCLTLPDTLITVMGIEKVLPRFQDIEVFAQLLPRSSTGERMNPYTTMWSGITPGDGPQQFHLVLLDNGRTKALADDVGRQALHCIRCSACLNVCPVYEHAGGHAYGSVYPGPIGAILTPLLRGTGTAPGPLDLHDPTASLPFASSLCGACFEACPVKIDIPTVLVHLRNRVNEAQQRRALPTGWQAAMGATSALMASGRRFGPAAATARAGRLLAGDGRIGHLPFPGSLWTDSRDLPAPPHETFRSWWASHEKARKPRGDGGGENGGRGAGES
>NZ_CP040915|725198:791602|756174_759075_-|WP_139927254.1|DBSCAN-SWA
MNKLVEVRLLGPFEVLAGGQPANVGGGKRRGLLALLALRCGRVVGVDSLIDALWADDLPAAPRNAVQHHVARLRAALGSEAIAATPDGYALAHAAVDALRFEDLLHEARDALRAGDAVAGAESVARGLELWRGPALHGLTDTAWFGAEARRLESLRVDALEEQFEAALVLGEHRDVVPALGTALEENPFRERLWGQLMLALYRSGRQPDALEAFREARRVFSEELALEPGPELRRLQDAILSHDPAIAPLPAPRRRRGTLPAPSTSFVDREEALAQVLALVREHRLVTLTGLPGVGKSRLALEAARSVEHEFADGAWFVDLARAGGEDDVVRLVAHAVDVRGADPLARVVGRLRDADAILWLDGCGRVVGEAARVASAVVAGCPDVRVLTTSREVLHVPGEVRVMVEPFRVPDPGRSDGVDSPAVQLFVERARAARPGFELTAEAAPLVAKISRHVDGLPLAIELAAARAHALGLVEILSVVEHRLELLGDVPASDANRASLQALVEWCYDVLHEDEKSLLHKVAVHRGGASVPSLVAAAASDGLDEPTVTYLLGVLVDKSILAVSFPAEGARYDMLETVREYALERLAESGRLAAARRAHAESIAALAEAARAELRGADWRAWVRRLELENDNVWAALTYARDARESGIAARLAALAWYFVLAERVAEGRRFLERALAATSGDLTVAERLELHAFRCYLATEELDLDTAIEIGERALAGEATEAAVPELGLVEAALGLAVAEAGDVERGAALAGRGYARLDAGENHWESAAASLFCAQVAAAAGDVATVAAMAAEARRHAQATGFDAFLVPAMLLEAWVAERRHDSSAATVAYRRTLDLAGRIGFADHAAFALSGLASSALAGGDVTQAEELERRALATAEAARASWAAAHARVELGRILAAAGDAKTAAKLYRTVLAWSKARRAHGPRESLFVVLSQDPAAAAAVGLAGLGDGRDEITAATAPA
>NZ_CP040915|725198:791602|791224_791602_-|WP_139927283.1|transposase|DBSCAN-SWA
MSTKRCPDDLKDRAVRMVLDHQSDYASQYAAIKAVAAKLDIGAESLRLWVRKSEVDTGKRPGVTSEEYARVKELEREVKELRRANEILKAAASFFAREPDPPRRWSAGSSTRTRTGSGSSRSAPC
>NZ_CP040915|725198:791602|762614_763067_-|WP_139927257.1|DBSCAN-SWA
MAMNTTNPLEKAASTLRQHTDRGWMAIRADVFSHALAMFRPSAPVRGVHGAGEFFLAADVLVAHLRDALDAIPRAGVSRITCTTDADHNLEAVTVEIIALYRARLVPLAEMIRHRAAELLVQVLGLSPEQLRDVPVHVGVTDVTNDAALL
>NZ_CP040915|725198:791602|755536_755962_-|WP_168205568.1|DBSCAN-SWA
MQRYVDALHGDEEAARASGRTEAAAVAGRLEQLDISLEIAEHRMAAELAATEEQFTGAVEAELHRWDAYLDRMQTKAATKTGVARDRAEAAIADLRQRRLAIGARVAAAGTATDDGWRDAKTHALAELDELNAKAATAWRD
>NZ_CP040915|725198:791602|773166_774690_+|WP_139927268.1|DBSCAN-SWA
MTPPRLELRSISHNFFNVPVNKDISLSVAPGEVLGLVGENGAGKSTLMNVVGGVMQPTEGELFVDGEPYAPSSPAEAARRGIAHVHQELNLFANLSIADNIFLTNYPRRAGIFTDRRAARERSRRALDLMALPFSPDTRVERLSPGQRQMLEIAKAAVGEPGLIILDEPTTSLTSRETERLFQLIADLTASGTSVVYVSHILEDVKALSDRVAVMRDGNLVDVRAASDAPIGEIITLMVGRRFDQRFPDRDGAPTSEPVLTLDGVCATGLVDDVSLTVHRGEVVGLFGLMGAGRTELARIIAGLETADAGTITLNGADVGSTSPRQRIAAGLALVTEDRRGDGLLMDFPVITNAALPSLGRWSRHPVAPVQRRRLRRDVAAIAEELRIKTSSLREAPVRSLSGGNQQKVVLAKWLLTEPSLLILDEPTRGVDVGAQFEVYRTALALADRGAGILAISSELPELLGMCDRIGVMRQGRLVAEFAKADFDSRAILGAAFGEALVPGKVG
>NZ_CP040915|725198:791602|772084_773170_+|WP_139927267.1|DBSCAN-SWA
MSIAQARRRVIERPPDSQRVDAFRRFFAGEGFVAALIVVYVVVVSQFADGMLTSRNLLNVLSNLWPLAIIVIGQAFVLILGGIDLAQTAVANITNTFGALLLAQSLSPALFGDTVFWGSLVGESGGVLRDGGVAPAVVIVLVLGLGLGALNGLAVARLHMPPFMVTLGAMLLLGAVAVWMTRSENVASLPEAYLAIGNKGLGGPFTYAMVIAVVVGLASHYLLARTPFGAWLYAAGTNRQTSIVSGVPHDRTVVIAYALSGLLATVGGILYSTRLQAGRPTLADDMLLDIIGAAVIGGLSLFGGKGTILGAFLGAVFFVVLSNSLNLLNLPFTVVFIVKGLVIVAAALLDVARARLTGADR
>NZ_CP040915|725198:791602|774701_775682_+|WP_168205573.1|DBSCAN-SWA
MRSLALNNTPVLLLVVVFLVFSVADARFFDVHTLTNVARSAAYIGILAVGMTLVLMTAGIDLSVGSMMYLVAVVVGQVANSYALPVFLVPVLAMAVGLTFGALNGFAISVLRVVPFIVTLAMLTAYRGLGLELSESREVNYPDVIGQLGAQPILGVPLPVWVFVVVVVLAHVLVTRTPFGRQLLATGEDRRAAERAGIPVRRILFTVYVVAGALAGLAAFVAMTQLRTAAPGFGTADEFDAIAAAVLGGTSLFGGRGSVFPGTVVGVLLIQLIQTGLQFMQVDLYITPMVQAAIILLAVFVDSARTGRLERLGRRHITSSRMETAA
>NZ_CP040915|725198:791602|728549_728870_-|WP_139927232.1|DBSCAN-SWA
MTPEQALGHIAAVLRARSDADLGPETITMLDDLLNVGHTITEERQEPARFVIAVRELAETLAESIAPPSAEADTARDEEAEPPAAVVQPDTVELVLLHLCPLWPLC
>NZ_CP040915|725198:791602|749472_750804_-|WP_139927247.1|DBSCAN-SWA
MTSAKQLKTRVRARMARTGERYAVARAHVLRPAGGAGDPIVDAGWALRGGADPDTAALTNVLAHRGVTGPHGPLTEPLLFVVGGGLGAGYILWEFAHDDSRIVTLGFAHSWQYFDRRLTTTVDRLGLDVTWSRTGGAAGAARALRSALAGGDPAIVWPDRYHMGYWHVPALLDGAGGHPVVAYALSEDRSGGRVHVDDRTLAPLTVPAADVDRARARVGSYKNTMLVVRSADTVVSADQLRTAVRAGLQATVDHLGGTSTSFALPAWRKWSRLLVDSRAEKGWPTVFADGRGLLRALADVWEAVEPAGMDGGHLRDLFADGLEQAAVVLDEPALAAEAPLWREIADRWHTLAESALPDDVPAIARLRELTATVTGAVAEGDATADDRAAAAEELWQLRAAHDDAPPLDDERLTAVLATMSAHVAAIHDAEAAAVARLGAIVAG
>NZ_CP040915|725198:791602|732554_734531_-|WP_139927235.1|DBSCAN-SWA
MTNEAKRLLVGQPLRTENLGQQLLPKRLALPVFCSDPISSVAYATQEILLVLALGGSMLLHLTRGVGLAILVLLGIVVASYRQICFAYPSGGGAYIVSRDTLGERASLVAAAALLVDYVLTVAVSMVAGVDAITSYAPALNRHAVALSLGFVLLLMLVNLRGLKESGRGFAAPTYAFIAGIFLMFAVAAWRVMTGQHLHAVSADFHVQPAPHLPGLLLVVLVLRAFASGCTALTGVEAVSNGIPAFRPPKSRNAATTLAVMGVLSATMFGGITLLALLTHVQMVDEPGRLLGAPAGYVEPTALAQIADAVFGPGPLFAFIQAATAGILVLAANTAFNGFPVLTSLLARDGYLPRQLHHRRDRLVFSNGIIVLALAAGLLVVVFDADISRLIQLYIVGVFVSFTLAQAGMVRRWQRDRARATDRQRQRIRRGQVINALGAVTTGLVLVIVVVTKFSHGAWIVCVAMPALFLLMRHISRYYEKVREETALHEEPTLPARNHAIVLVSGLNLPTAQAVAYARAIHPASLEALTVEVEQDETEELKRAWADHHLDVDVPLVVLYSPYREITRPVVDYVRTYPRTSPRDVITVVIAQRVAGRWWEQPLHNHSSLRIKSRLLFQPGVVVTSVPYQLRSATDRAHRPDTGDRDSLLLLAARHASP
>NZ_CP040915|725198:791602|777913_779752_+|WP_139927272.1|DBSCAN-SWA
MTERGGPLNLVAGAWTATLNPDGVLADIRFGGHLVLKALMVVVRDEAWGTVPGTVTVAPHHTDDGFDVRLAGEHVYGPVDFVWDGHVVGGPEGLEYRFDGRARTAFDSNRIGFVALHPLEPAGRPVGVLRVDDAWVQGQEGDVVVTESRFPADVVPHQPFVGVAGFVEHTPHGDVTIRFRGDTFETEDQRNWSDASFKTYSRPLAQPCPVHWQAGDETAQAVRLTAAAPGAFSPWPASSASTQPYPATATVVVDDVPARLPHVGVTVGPEDNPALLGAEIAALRPHHLRVDVHAGPGALRGGEVLTAAGRAGIPLQVAVHVDTDPARALGDLRQRLAGVDVASVAVFDATAPSTTTRAIDAVRGVLGTALGAVLILVGTDDNFAELNRNRLSLDDFEASAAVFSLNPGVHDIRSAAVLETVEAVPVMLATARSFVGGPVAVGPVSLRPRRNIYRAGVAIDRTGRDDGSVDERQHAAFAATWLIATLASLIAAGAQEVTVFELSGPRGLVDRPGGRRSPAFEVVRAVTAGTGALTCKTDDTRLAVVALTSRRDGDGRSTTTAPPTTTVLLANRSTDTVDVRIEPAGVSVILLPHGYAVADLPGAPSAHLEELP
>NZ_CP040915|725198:791602|763057_763609_-|WP_168205570.1|DBSCAN-SWA
MPSLSDLPDAVLARRAALRDHAAFGVIVDRHGPALYRYSYRMLQHHSDTQDCLQDVMVAAWRGLPAFRGDAALRTWLFALTINQVRTFLRRRPPSTLPVDSLQIAAPGRFDPEQQALAADLLSALDRALRELPLSQRSTWLLVEIEGLSYADVADIRHTTIDAVRGQLHRARHSLETKLEGWR
>NZ_CP040915|725198:791602|753545_754214_+|WP_139927250.1|DBSCAN-SWA
MTSPAGADASVPRTSAARPAGPPSERLAARLEVRDATPPAVLDDLTRLDLAAYRAIAETPTPTLDEPLRRLSIVASHSKLWMGIAALIAAFGGPSGRRTAVTALTAVGVNSLVVNLPLKLLGRRARPDRAAARVSPTRHVPMPTSPSFPSGHAASAFAFVAAVARTMPGVARYMRALAYLVGYSRVHTGVHYPGDVIVGAFIGTAIGESVAYAASPRPRSWL
>NZ_CP040915|725198:791602|748834_749287_+|WP_139927246.1|DBSCAN-SWA
MDVDRSAPVQRRDALEIDASPDVVWSVLTDLESWPDWMPGVRSVEVEGPFAVGMQFRWKSGGTRLVSTVMDASPGHSAGWRGKTLGIEASHVWRLQSQDGRRTHVVTEESWSGVLPRLFRRYAERIVSKALAEGLAALGAEAARRKRPPH
>NZ_CP040915|725198:791602|765924_766506_+|WP_139927263.1|DBSCAN-SWA
MSRAVLALDRTLAFLLGLLLLAVGAAAVAWWAGELDRVWPTVPDTLRLGDASSAVGAPWWPWAAGVAGVLAMLLGLRWLIAHVPRRNVGTLALPGTPGRGSLRIDPGAAATTAAQVLAETPGVRSVRGTMHDDRGELVAALSATIEPTADLATVVDRAERVSAELGHVLGIDAARCRVQLSVARRGRRLPRAE
>NZ_CP040915|725198:791602|738061_738736_-|WP_139931297.1|DBSCAN-SWA
MRLLVVEDEPSMRSLLARSLQREGYAVDVAATGDEALWSVSENAYDAVVLDAMIPPPDGFEVCRRIRAEGRWVPVLMLTARDAVPDRVRGLDAGADDYLTKPFALAELYARIRALTRRDPLERPAVLQVGDLMLDPASRLVRRGDVDIALSPKEFALLHELMRRPGEVHSRTALIDHVWDFAYDGASNVVDVYVRYLRDKVDRPFGRDTIRTIRGAGYRLDPEG
>NZ_CP040915|725198:791602|729177_731802_-|WP_139927233.1|DBSCAN-SWA
MTLMTPDAAVGTDRRPPEPPVPPTHDILLVDVPAVPLRRPGDLVGLTLSLAGIAAVLVLAVYAPRTTRAVSGDVATALAVVRSLLLAPLTALEGVAAYLVPAAVLVAAVSRRALRTAAGMVLAAAASVLAAVVLLRLGGHLTVVEGVLDPAAPAGSELVGASPYVAGLTALLTVAASDMRHRAVPWTLLWVVLGVSVIQGRQTMAGAAVFVLLGHAVGLLLRYLLGAGSDRASGPALVRAVRRAGLDPVRILRRDVPADGVRAVAWRVRTSAPVGYPEPRPFGLARPIPEDVGAGTSPPGDSITVDEITDAVAARAGMADAADQDGARDGARHYAAWDTEERRYDISVLDGDRQVLDYLGGLWDTLRIRGLRRRGGSNLRENAGHTILMILWAQHAGVRTPPLVGVAAARNSVIMITAHIPGLRPLADLPAEELDDTVLDDVWQQLRAAHGRGLSHNDLDARSVLVDAGRRVRLAHWDHGDTLASELAQRIDLAQALVLLAVHAGPDRAIASATRSLGRANLAAVAPLVQPVALPASTRVALRPRRHLLEDLRRNPAQLVPTASTEPARINRFSPRTVVLVVVGGVAAWVLMGSLGSEDVASAISGARPGWMVAAFLLGMVTYLGSSLGLVAFSPERLGLVRTTLVQLAASLLALVVPAGVGPAGLNLRFLQRRQVALPVAIATVGLTQLMQFLMTMLLLVSTALLTGSVGTLTAPSPVLVIVVLGAAMALMAALALPPVRRWALAKVRPTLAQLGPRLSWLTGHPSRVALGALGGLLLSAGYIAAFGASLAAFGDTLPLVTLAITYLGASAAGSLIPSPGGIGPIELALTGGLTVAGMPYGTALSTTLLFRLADLLGTRTPRLAGSPRSGAPR
>NZ_CP040915|725198:791602|763863_764313_+|WP_139931299.1|DBSCAN-SWA
MTSRPTGATNVGTATVVSALSSSKGTTTINDVVVSKIAGIATNEVDGVHAMGSGAARAMGSLRERIPGSTTNQSRGVTVEVGETQAAIDLSIVAQYGVAIADLAEGIRRNVIASVERMTGLEVVEVNINVTDVHLPEDDVAPEQEQRVQ
>NZ_CP040915|725198:791602|779748_781005_+|WP_139927273.1|DBSCAN-SWA
MTDRIRARYLIETPASPARAAAAMAGEQSTGTFIAVPGETPEIHRRHAARVEDVVELDEHDEPALPGSRGGSPFHRAEVELSWPLENVGTSLPNLLATVAGNLFELQQLSGIRLEALGLPAELSRAHPGPQFAIDGTRRIADVWERPIIGTIIKPSVGLTPEETGVLAGALSRAGLDFIKDDELMANSPHSPLEPRLAAVLAALDDAASETGRMPLYAVNVTGEIDEMLANVDRVAEMGGNCVMVSVNAVGIAGLRAVRQHSALPIHAHRNGWGALTRDPMLGYSYDVWQQLWRLAGADHLHVNGLRNKFWEPDDSVLASARAVLAPINGGPPVMPVFSSAQSAEQVADTYQALGSTDLMYICGGGILAHPDGVAAGVASIRQAWDAALGGVDLDEHASTHPELATALATFRNRHELS
>NZ_CP040915|725198:791602|754887_755526_-|WP_168205567.1|DBSCAN-SWA
MKMESTYDPGPALRAGELIFARVWKLIALRGVVAIAFGIVLLVWPDVGLTAIVSAVGVLAIASGSVSAAAAFGLPGAAKRYRFWLAVHAVVGLLAGAAVLLWPDLSATALLYAIALWAIAVGVIELVGAFVLPLSGPRTVLVAVGGIAFAAFGVVMFVEPSGGAMALVALVAAFALVRGTFDVALAILLRHVAGELDQLFRSPSGAEAATHG
>NZ_CP040915|725198:791602|746154_746442_-|WP_168205561.1|DBSCAN-SWA
MAVLVVARMTGNPDELAEKVLEHLTPVMNEVARQRGAVWHALAKTPDGVMVVDVWESADAVTAAVGEQRVQEAIERSALPQPQFDIYDLVEHRNP
>NZ_CP040915|725198:791602|775678_777040_+|WP_139927270.1|DBSCAN-SWA
MTPPDVPTGHHGLALTFYGDDFTGSTDVMEALTLAGIPTVLFLDAPTPELVAVHRDALAVGVAGISRTMSPEEMDATLPGIFTRLAGLRAPLFHYKICSTFDSSPHIGSIGRAAEILRRIFPGYPMPLLVAVPQLGRYTAFGHLFATAGRDVHRLDRHPVMSRHPVTPMSESDLLVHLAAQTDLPTALVDLRALGGPDAAVDERVDAVLASGAQIVHFDTVDAATQRQVGRTLTRLAEGRPDGQPLVVIGSSGVEYALDLAWPEGRRASVGQPDEPADVDQTLAIAGSRARETDEQVALAIENGFAEVRVDPAAATGPDAAAYATAVVERAAAAWRRGGHVLVRTPPKSGTSDVDGNLLGAALGRIASELGLLVDVRRLVVAGGDTSGFVARALGIETLRLVRQLAPGAPLCRATSRNGRFDGLEICLKGGKNGTPDYFVRIAALASSRLLNL
>NZ_CP040915|725198:791602|766725_767208_-|WP_139927264.1|DBSCAN-SWA
MGTKARIGSLAYVLSALKHLRDRPMRVQIQIDDDPPLRRRARTVVIGNVGRLQGDVQLLADAKPDNGQLDVAILAPRHLAHWAALAWGILRRHEHVPRIEVLRGARVTVTSDRNQPCQLDGDVIDPRRTLAVIVRPAALWLCVHQPDHSPDLTAGSPKQR
>NZ_CP040915|725198:791602|784629_785292_+|WP_139927277.1|DBSCAN-SWA
MSDAREAVLARIRDALGRTPAAPLSPVPRAYRSRSDLAPGSVEAVDGLVDRLEDYRARVRRCTEADLAPTLAALLADAGSVVVPPALPAAWLAGLPGGATVRTDSPDAPLTNTELDGVGAVLTGARVAIAETGTIVLDGEPDQGRRVLTLVPDRHVCVVAAQQVVATVPEAIAILGAHPARPLTWIAGPSATSDIELQRVEGVHGPRTLDVVIVGLEGSR
>NZ_CP040915|725198:791602|748287_748431_+|WP_168205564.1|DBSCAN-SWA
MKAVGSGESPDQRPSAFPGVLDRQGLIIDERRYYDVADQLEQLGLSE
>NZ_CP040915|725198:791602|769015_769786_-|WP_139927265.1|DBSCAN-SWA
MTEHPGRVLEGKVCLVTGAASGIGRAVATRFVRSGAVVFFADRDGEGASTAARATRSTGASPVVLDIADEQSVEAAFAEVLAVAGPPDVVVANAGIQDFRADGPIGELTLGSWRRTIDINLTGTFLTLKHAVRTVRRPGSSVIVTGSPTAINGEGAGFTAYATSKAGIHGMVRVAAADYAGTGIRFNTVVPGFTMTPLVADIANDTSKRAAAVSRVPLGRAGRPEDVVGIMEYLASDESSYATGSLFVVDGGMTSL
>NZ_CP040915|725198:791602|761107_761926_-|WP_139927256.1|protease|DBSCAN-SWA
MVTSAAPRVHDTPLIGLLPTAGVSLSAFLLFALQLAGWGHALLVVSLLGAWAVSRELVKDLALVGIGITIVSTTSVEADVSWDRFFTIGTVLLSAVGLPYLVDRFVYRREAIRFPWRTGQRWTRLEKGYLVAVPVLGWLILPYYFITSGAYLNWPNITDRSELARFFVGVNFVGTWDELFFICTCFALLRRHFGMWQANVLQAVIFVSFLWELGYREWGPFLTAPFALLQGWIFSRTGSLTYVLIVHLLFDVFVFLAIVHAHNPGALPIFLV
>NZ_CP040915|725198:791602|731798_732440_-|WP_139927234.1|DBSCAN-SWA
MNQHDLTAARPDVPDRATRPPRRLGRGATRAQHPPVPRQKWPAVVMAAFAGVVFAVGLSWFHNGAESLVGLHQVVAVGVQRQAHGLQMLDLYIVPTAAASGTPAPASWELAGALVITHGSEDRLVGAKIDGRQATVTAGAGTPGAVTVTTERPTPVGLAAGDARVTVADPALRAGTVVPVTLTFAHRGDVHVSVPVLVSAAGPSDAATAGGAG
>NZ_CP040915|725198:791602|747244_747916_+|WP_168205563.1|DBSCAN-SWA
MWQRRTRVLICQSVHTPKEKHMAAIENVVVVRFTEPSKAYQALSALKDCDAEGRIALRSAAVVERTPEGFLRTPEAADNIGLVGTASGSLLGMLIGVLGGPVGVLVGWGAGAVMGGAFDIGRAVKSDEALTELGRAIPPGSTAVIATAAEPAVEVIDGEMRKLEGEVTRRPVGDVMDELEAAEDAAEAAAREARRELREKRKTELSASVDARVGTLKEKLHIS
>NZ_CP040915|725198:791602|765250_765928_+|WP_139927262.1|DBSCAN-SWA
MTAHPPQDVSTPGARKAAAGSLVDDPEQGSWSSPAEPDREAWRPMLAASLPTRSGAIGVLGPVLATLLLAAGIVLVIEALVASGVLAGTGLVATGLATLNGLPPGPWFLVGGIVAALLGVWLIVVAVSRRVRSRVTVTSRTGIYLGVGDVARLASAAAEEVGGVISASTVATRRRVTTTIRSTGDAGIADAVRQAVADRLTMLDPAPRIVVAVRGKGRTTDGGTP
>NZ_CP040915|725198:791602|744205_745870_-|WP_168205560.1|DBSCAN-SWA
MRRDRSRRRAAYVAAAIGAVGLLSALSRPLRGRLAAVLDVVPVVVPTTAVLTLVFVSFALLLTALGLRRGHRLAWVVAELLLFASVMLHVTKGLDVEEAAMAAAAVIWLGLRRRAFPVLPSQAAAARAVVVGVCGTVAVVVVSLVLAQMARGVGEVDDFVGLVLRDLGGAGRVPPPFTGRFAAVVLAAMGLALLGSVAWLLFSPRVPEPLVGEDHRRERERARSVVLRYGGGTLDYFALRDDKQWFFTGSSVVAHSVRGSICLVSPDPIGPAEEARETWADFTAHAERSGWSVAVLGAAEDWLGIYEASGLRPVYLGDEAVVDCITFKLEGHAMQSVRRAHRRVRAAGYTIAFHGTADLDPATRAELLGLAGQSRRGEGERGFSMTLSRLFDPADTGVVVAVARDAAGRAQAFSQWVPATKLPGWSLDVMRRSMAPDLPNGIMDFLIVETIWWVRQAGGTALGLNFAVGRRIVAGDNGVTATARLARQLLRRASNNMQIESLWRFNAKYGPRWVPRFAAVGTLDLLAGQGLAMADAEGLTELPLVGRMVGRAPR
>NZ_CP040915|725198:791602|734535_736446_-|WP_139927236.1|DBSCAN-SWA
MTGIEDYALLGDLHTAALVSREGSIDWMCVPRFDSGACFAALLDTAEAGRWLLAPAAGGPCSRRRYRGDTLVLETEWDTPTGSVRVVDFMPPRGETPHVVRLVQGVRGTVPMSGELRLRFDYGHVVPWVRNIGGAIEAVAGPDAAWLRTPAPLRGQDNRTVSEFVVRSGQTVPFVLTWAPSHLATPDPLDPEQALRDTVDFWERWSARSSATGRWRDAVQRSLIVLKALTYAPTGGIVAAVTTSLPEQPGGPRNWDYRYSWLRDATFTLQALLAAGYAEEATAWREWLLRAVAGDPGTLQIMYGLDGTRRLPETPLPWLAGYEGSTPVRTGNAAAGQFQLDVWGEVLDGLHLARQANMAADDDAWDLQVALMDHLEGHWRDPDNGLWEMRGPRRHFTHSKVMAWVAADRMARAVRESGLPGPLRRWQDLRDDIHADVLSHGYNDERGTFVQSYGGTELDASLLLIPRVGFLPGTDPRVLGTIDAIQRELTQDGLVLRYRTETADDGLPAGEGVFLACSFWLVDALHYAGRENDAIALFERLLAVRNDVGLLSEEWDPRMGRQLGNTPQAFSHFPLVVSALQLAQRRPRHSDQPMSAALPRELQPVNASSERHPAGYRRQHQAGPISHGPLMRGLRG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
719298:719315	attL	NA	NA	NA	NA
WP_139927229.1|725198_726554_+|integrase	tyrosine-type recombinase/integrase	A0A0U4B2E0	Arthrobacter_phage	8.9e-34	31.3
WP_139927230.1|727425_727782_+	hypothetical protein	NA	NA	NA	NA
WP_139927231.1|727989_728178_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_139927232.1|728549_728870_-	hypothetical protein	NA	NA	NA	NA
WP_139927233.1|729177_731802_-	UPF0104 family protein	NA	NA	NA	NA
WP_139927234.1|731798_732440_-	hypothetical protein	NA	NA	NA	NA
WP_139927235.1|732554_734531_-	amino acid permease	NA	NA	NA	NA
WP_139927236.1|734535_736446_-	glycoside hydrolase family 15 protein	NA	NA	NA	NA
WP_168205559.1|736432_737038_-	DedA family protein	NA	NA	NA	NA
WP_139927237.1|737408_738065_-	DUF1345 domain-containing protein	NA	NA	NA	NA
WP_139931297.1|738061_738736_-	response regulator	NA	NA	NA	NA
WP_139927238.1|738764_739283_-	hypothetical protein	NA	NA	NA	NA
WP_139927239.1|739570_740902_+	HAMP domain-containing protein	NA	NA	NA	NA
WP_139927240.1|740972_741905_-|protease	PrsW family intramembrane metalloprotease	NA	NA	NA	NA
WP_139927241.1|741901_743899_-|protease	ATP-dependent zinc metalloprotease FtsH	A0A0P0CCN8	Ostreococcus_mediterraneus_virus	2.7e-103	47.6
WP_168205560.1|744205_745870_-	DUF2156 domain-containing protein	NA	NA	NA	NA
WP_168205561.1|746154_746442_-	hypothetical protein	NA	NA	NA	NA
WP_168205562.1|746829_746994_-	hypothetical protein	NA	NA	NA	NA
WP_168205563.1|747244_747916_+	DUF1269 domain-containing protein	NA	NA	NA	NA
WP_168205564.1|748287_748431_+	hypothetical protein	NA	NA	NA	NA
WP_139927246.1|748834_749287_+	hypothetical protein	NA	NA	NA	NA
WP_139927247.1|749472_750804_-	DUF4872 domain-containing protein	NA	NA	NA	NA
WP_168205565.1|751266_752118_-	hypothetical protein	NA	NA	NA	NA
WP_168205566.1|752201_753170_-	magnesium and cobalt transport protein CorA	NA	NA	NA	NA
WP_139927250.1|753545_754214_+	phosphatase PAP2 family protein	NA	NA	NA	NA
WP_139927251.1|754250_754895_-	hypothetical protein	NA	NA	NA	NA
WP_168205567.1|754887_755526_-	HdeD family acid-resistance protein	NA	NA	NA	NA
WP_168205568.1|755536_755962_-	hypothetical protein	NA	NA	NA	NA
WP_139927254.1|756174_759075_-	AfsR/SARP family transcriptional regulator	NA	NA	NA	NA
WP_168205569.1|759388_759997_+	DUF1269 domain-containing protein	NA	NA	NA	NA
WP_139927256.1|761107_761926_-|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_139927257.1|762614_763067_-	hypothetical protein	NA	NA	NA	NA
WP_168205570.1|763057_763609_-	RNA polymerase sigma factor	NA	NA	NA	NA
WP_139931299.1|763863_764313_+	Asp23/Gls24 family envelope stress response protein	NA	NA	NA	NA
WP_139927259.1|764309_764702_+	hypothetical protein	NA	NA	NA	NA
WP_139927260.1|764704_764884_+	DUF2273 domain-containing protein	NA	NA	NA	NA
WP_168205571.1|764876_765254_+	Asp23/Gls24 family envelope stress response protein	NA	NA	NA	NA
WP_139927262.1|765250_765928_+	hypothetical protein	NA	NA	NA	NA
WP_139927263.1|765924_766506_+	hypothetical protein	NA	NA	NA	NA
WP_139927264.1|766725_767208_-	hypothetical protein	NA	NA	NA	NA
WP_139927265.1|769015_769786_-	SDR family oxidoreductase	Q06VL0	Trichoplusia_ni_ascovirus	6.4e-13	30.4
WP_168205572.1|769782_770601_-	FadR family transcriptional regulator	NA	NA	NA	NA
WP_139931301.1|770993_772019_+	substrate-binding domain-containing protein	NA	NA	NA	NA
WP_139927267.1|772084_773170_+	ABC transporter permease	NA	NA	NA	NA
WP_139927268.1|773166_774690_+	ATP-binding cassette domain-containing protein	W6JKT0	Anomala_cuprea_entomopoxvirus	4.5e-10	23.8
WP_168205573.1|774701_775682_+	ABC transporter permease	NA	NA	NA	NA
WP_139927270.1|775678_777040_+	four-carbon acid sugar kinase family protein	NA	NA	NA	NA
WP_139927271.1|777054_777903_+	NAD(P)-binding domain-containing protein	NA	NA	NA	NA
WP_139927272.1|777913_779752_+	hypothetical protein	NA	NA	NA	NA
WP_139927273.1|779748_781005_+	ribulose 1,5-bisphosphate carboxylase	NA	NA	NA	NA
WP_168205574.1|781090_782164_+	NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_139927275.1|782183_783071_+	(Fe-S)-binding protein	NA	NA	NA	NA
WP_168205575.1|783001_784633_+	lactate utilization protein	NA	NA	NA	NA
WP_139927277.1|784629_785292_+	LUD domain-containing protein	NA	NA	NA	NA
WP_139927278.1|785217_785988_-	DUF2306 domain-containing protein	NA	NA	NA	NA
WP_139927279.1|786031_786499_-	hypothetical protein	NA	NA	NA	NA
WP_139927280.1|786715_788998_-	AAA family ATPase	NA	NA	NA	NA
WP_139927281.1|790583_790988_-|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A1B3AZE5	Gordonia_phage	3.0e-22	56.2
WP_139927282.1|791015_791231_-	hypothetical protein	NA	NA	NA	NA
WP_139927283.1|791224_791602_-|transposase	transposase	A0A1B3AZF8	Gordonia_phage	3.2e-18	50.5
791369:791386	attR	NA	NA	NA	NA

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP040915|2072352:2083359|DBSCAN-SWA
CATGAAGCCTTCCGAAGCCGCCAAGGTCCTCACCTACGTCGCCGCGTTCAACGGTCGCACCGTCGGCAAGACCGACGCCATGGCATGGGCCGACGCCCTCCACCCTGACGTCACCTACGAGGACGCCAAGACCGCCGTTGCGCAGCACTTCGCCGAGTCGACCGACTGGTGCATGCCCGCCCACATCAACCAGCGCGTCAAGACCATCTGGCGGGAGAGGGTCGACGCCATCGGCGGGGCCGTGCCACCCCCTCCTGACTCCATCGCCGACCGGCCCGGCCACTGCTACAGCGAGTGGCATCAGGTCTTCCTGCGTGCCGTGAAGATCGGTGCCACCCCGGAAGAAGCCGACCAGCAAGCCTGCGCAGCCGTGCAGATCACTCGCGCTCCCAACGATCCCCTCCGCTCACTCTCCTGGCGCCGGGCACAGCGTGAACAGCAGCAGCTCGGCGCCGCCTGATGTCACGCCGGCACGACCCACGCGCCCTCGACACCCCTGAGCGGTCAGAGGGCGCGTGGGAGTACGAGACGTGGGCGGCACAGTGGGGCGACACCGAGACGACCACCCCACCGGCGGACTGGCAGGTCGCATGGGCGGACACCACCATCAGCACCGTCGAGAAGGTCTGGTCCGAGCAAGGCGCCAAGCTGTACGCCCCACACCGGTACAAGTGGTTGCGCGACGACCTCCACACCTGGCTGCTCATCGAGGCCCAGAAGGTCGCCGACTGGTACGTGCCCGTCCCCTGCCCCGACCCCGAGGGCATGTGGGCCGCGACCCTCTGGCGCACCCTCCGCAAGTCGGCCCGGTGGCACTTCGGCACCGTCGCCAAGACCGTCGAAGAACAAGACGCCTACCACCGAGGCGTGACGTCCACCAACTACCTCACGGCAGAAGTCGGCGATGCGTGGCTACCCCGCCACGCGATCCACGGCGACGACTGGACCAGCCGAGACCCCGCCGACGTCGTCGGCCGTGTCGAAGCCCTCGCCGAGAAGGTCCGCCAGGCCGAGACCTACACCCGCGAGCAGGGCAGCACGTACACCACCGAGACGTCCCCGTACTGCTCCGAGCCCCTATGCACCCAGCCCGTCGACATCAACGGGCAGTGCCGGCCCCACTACGAGAAGGAACGACGCCTCTGGGGCAACGTAAACGGGCGCCTCTGCAACATCCCGGGGTGCGGCAGGCCCCACCGCTCACGGGGACTGTGCAACACCCACCAGGCCCAGCTGCGCGGCGGCAGGCTCCCCGCCGAGTACATGCAGTACGCCGAGGCCAAGCAGCAGCCCGCCACCGGGTGCCAGGTCCCCGGCTGCGACAGGCCCCACGACGCCCGCGGGTACTGCGCCAAGCACTACGCCATATGGCGCAAGGGCACGCTGTGAGCGGGGCACAGGCGAGGGCAGGTCACACCCTCCCAAAATGCCCCCACCCCCCTACCGGGCAGCAAGGCGCACACCGCTGCCCCCACCGATGCGCGCACGCCCCATGCCCCCGAGGCCCAGCCCCGGCCCGTCCCCACGCGGAGCCGACGGGATCACCGGCGCGAGCAGTTCAACATCTGCGGAAGCGAGGCAAACACCATGAGTAAACATTCATCAGCCGGTTCAGCATGGCAAGCAATCAGATTGAGAATCCTGCAGCGCGACGGCTACACGTGCGCGTACTGCGGCAGGGAAGCAGACACGGTTGATCACATCGTCGCGAAAGCGAACGGCGGAACAGATGATGAATCGAATCTGATTGCAGCTTGCAGGACGTGCAACGGGTACAAACAGGACCGCCAACAGATCAGGGTCCCCTACGTCAATACCAAATGGCTGACCAGCGTCTGATTCGGTCGAGGCTGGTCAACGCCGCCGAGTCGAGATCGGCCCGTTTCTTTAGCAGGGCCCCGGCAGCCCCGCCCCCAACTGTCGTTTTCATGCGTGAAGCTTCAAATATTCGGAGGAGGTGGCCAGATGGCTGCCAGGACGTTCGTGTCGTCGCTGAGGTCGTTCCAGAAGGCGTCGCCGTGGTTGGGCCCGGAGCATGACCCGGCGCTGGTGATGCTCGAGGCGATGGCGAAGGAGTTGGACGGCGGGGAGCTGACCCCGGCGCTGCTGTCGCAGTTCGGTCTGGCCTATCGGTCGCTGCAGAAGCTGGCCCCGCGGTCGGACCGGGGCGAGGTGGACCCGTTGGACGAGGTCCTGGCCGAGCGGGGGCGCTGAGTGGTGTTCGCACCGGCGTTGATGACCCCGCCGCTGTCGGAGGACTTCACCACCGATGGTGACTGGCTGTTGCGGTTCGCGGACCTGGCGTGGTGCACCCCGGAGTCGCCGGCGGGGATCGAGTTGGACGCGTGGCAGCGGGAGTTGCTGCGTCGGATGCTGGAGACGTATCCGCCGGGGCACGAGCGGGCCGGGGAGTTGCGTTACAGGCAGGTGCTGGTGTCTCTGGGGCGCCAGAACGGTAAGTCTGTGATCGGGGCACTGCTGGGTCTGTACGGCCTTCTGCGGGCCCCTGGTGCGCTCGTGATCGGTGTGGCGTCGACGGCGGAGCAGGCGCGGATCATCTACGACCGGACCATGTTCGTGATCAACCAGAACCCCACGCTCAAGCGCCGGTTCGAGCGGCTGACCGACACTCGCGGCATCCAGGCCAAGGACGGCAGCAAGTACGAGATCAAGGCAGCGAAGTCCGCCGCGGTGCAGGGCCTGCCCGTCTCGCTCGGCCTGTTCGACGAGCTGCACATCGCCCGGGAGGAGGTGTGGCAGGCGCTGGTCAACGGCACCGGTGGCCGCAAGGACGGGATCGTGGTGGGGATCACCACGGCCGGGGATGATGAGTCGGCGCTGCTGAAGGGCCTGTACGACCTGGCGAAGAGGGCCGCGGGCGGGGAGGCGACCCTGGAGCGGTTCGGGGCGTTCATCTGGGAGGCCCCGGCGTCACGGGTGCCTGAGGACGACGGCGAGCTGCTGGAGTTCCTCAAGGCGGCGAACCCGGCACTGGCCGATGGGCGACTCGACGCCCAGAACCTCATCAGCGACATCCGCGCCATGCCCGAGCCCGACGTCATCAGGTACCGCCTCAACCGCTTCCTCGACTCCTCCGCCGCCTCGTTCCTGTCCCAGGACCAGTGGGTGGCCGCCGGCCGTGGGGATGGAGAGACGTTCCCCGAGGGGCGCCCGGTGTTTGCCGTTGACCGGTCCCCGGACTGGGGGTTCGCCACGGTGACCGCGAACGTGAAGGTCGACGGGGTGACGCACACCGAGGTCGTGGCGTCGCTGGTGAACCCCACGCTCGAGCGGCTGCTGCAGGTGTGCACGCAACTGTCGGTGCACTCGCCGTCCATGTTCGTGATGGACGGGTACGCGTTGCGGGATCTCGGCGGGGAGCTCAAGCGGCGGGGCCTGCAGGTGCGCATCTGCACTCAGGGTGACGTCGTGAATGCGTCGAGCCTGTTCTATTCCAAGGTCGTGCGCCGGGAATTGCGCCACGGCAATGACGGGCTGTTGTCGGTGCAGATTCCTCGCACGGTGCGCCGGAACGTGGGCGAGGCGTTCCGGATCTCCCGGAAGGATTCCTCGGTCGAGATTGACGCGGTGCTTGCGACGGCATTGGGAGTGTGGGCGGCCGAGGTTGAGACCGATGTCCCGGTGCAAATCTTCTAAAGCCCCGGCGCGCCCTGCGAATAGACTTGCATTAGCCGGTATAGTTATGCGTATGCGGTAGGACACTTCCTTGGAGGCTGGATGGGCTGGTGGGCGTCGTCAAAGTCATGGCTCCTCGGAGCCGACGATTCCGCTCACCTTCAGGCCAGGGCAGAGACGCCCCCGCCGTCGGACCCGTCAACGGCTCGCATAGCGCCTGCCAGGACTGACCTCTCGACTGCCTCGGCGCTGTCGCTGCCGTCGGTGTACCGGGCCGTGTCGATCTTGGCCACCGGTGTCTCCCAGCTCACGGTGGACGTGTGGCGCGGTGACGAGCCCTCGCCTCGCGTCCCGGCCTGGGTGCGTCGCCCCGACATCAAGGTGTCCCGGTCGGCGTTCTTCGAGCAGACCACGGTAGGCCTGGCGGTGACCGGCAACGCGTTCTGGCGGGTGCACCGCGACTCGGCAGCCGACCCGGTGCAGGCACTGACGGTCCTGAACCCGCATGACGTCGTGATCAACGAGGACGGCACCTACGGCTACCAGAACCAGCGGCCGCTGCAGGACTGGCAGGTGCAGCACCTCGCCCTGCTGCGGGTGCCAGGCGCCCGGTACGGCCTCGGCCCGATCCAGGCCGCCCGCGCCGACCTGGCCGGCGTGCTCGATCTGCGCGACTACGCCGCCGAGTGGTTCAACACCGCCGGTGTGCCCAACGGAGTGCTGTCCACCGAGCAGGTCCTCGCGCCGGATCAGGCGGCGCAGTACAAGAAGCAGTGGATGGAGCAGCAGTCCCACAAGAACGGCCCCGCGGTCCTGGGGGCCGGGATCGCGTACTCGCCGATCATGCTGTCCCCGAAGGACGCCCAGTTCCTTGAGTCGCGCCGGTACACGGTCACGGAGATCGCCCGCCTGTTCGGCATCCCTGCGTCGTTGATGCTCGCCACGGTCGACGGGGCGGCGATGACTTACCAGAACGTCGCGGACGCGGACCTGTCGTTCGCCCGGTGGACGTTGGTGCAGTACCTGCGCGAGATCGAGGAAGCGATCTCCACTCTGCTGCCCCGTGGCACCGAGGCCCGGTTCAACCTTGACGCCGTGCTGCGCCCCTCGACGAAGGCCCGGTACGACGCCCACAAGATCGCCATCGAGGCCGGGTTCCTCACCGTTGACGAGGTCCGTGCCATCGAGGGCCTCAAGCCACTGCCAATGAGGGAGCCCCACCGATGAGCGAAGAGCTGTTGACGCGGGAGGCGACGTTCACGGCCTCCGATGTGGAGGCCCGTGAGGTCGTCGGTATCGCGGTGCCGTGGGAGCAGCCCACGGACCTGGCCGGCTACAGGGAGCAGTTCGCCCGAGGGTCCGTCGTGGACTCCGACGAGGCGCTGCTGTTCTACGGGCACGCCGAGCCCATCGGCCGGGTGATCCGCGCCGAGGACACCGACGCCGGGTGGGAGATCACCGCCCGCATCTCAGAGACCGCCCGCGGGGACGAGGTCCTCACGTTGCTGCGGGACGAGGTGCTGACGAAGTTCTCGGTCGGGTTCCGCCCGGTGGAGGCACGCACCGAGGAAGACGGGTTGGTCACCCGCACGAAGGTCAACGTCCGGGAGGTCTCGGTCGTGCCGTTCCCCGCTTATGCGGGGGCATCCATCAGTGAGGTCCGTGAGCGGCCCTCCGACGAGGCGCACCAGCGCCAGGAAGGGGCAGACATGCCCGACAACGTGACTGCCGCGGACCTGGAGCAGGTCCGCGCATCCATCGAGGACCTCGACCGTGAGGTTCGCATGATCCAGACCGACAAGCCCACCGAGCCGGTGGTGGACACCCGCTCCGCCGGTGAGGTGCTCAAGGCCATCGCCTCCGGTGACGAGGCCGAGCTGCGCGCCTACACCGGTGGCACGACCGCCGACACGGTCGCGAAGAACGGCTGGGTCGGTGACCTGACCCGCCTGGTCGACGAGGCCGCCACCCTGCGTGGGCTGTTCTCCACCGGCAACCTCCCGGCCGAGGGTAACTTCATCGAGTACGCCGTCCTGGGTGAGAACACAGCCGTGGTCGGCGACCAGGGCGGCGAGGGCAAGGACCTGCCGTACGGCAAGGTGACGGTCACCACGGCCACCGCCCCGGTGAAGACCTACGGCGGGTACACGCAGCTGACCCGGCAGGAGATCGAGCGGTCCTCCGTGGCCATCCTCGACCACAACCTGCGCGCCCAGTCCATCGCCACCGGCAAGGCCCTCAACGCCGCGTTCCGCACCTTCTACGCCGCCCAGGTGGCCGCACAGACCTCCGCCGGCAACACGGTCGAGATCCCCGCCGCCGCGGACTACACCGACTGGCTCGGTGCCGTCGTGGACGCCGCTGAGAAGTACGAGGACCTCGGAGTCTCCCTCGACGCCCTGGTCGTGGACAAGACGATCTTCAAGACGCTGCTGGGCTTCACCGGTAGTGACGGCCGCCCGATGATGAGCGTCGACGGGTCCGGCGCGAACACTGTCGGCTCCCTCGATGTCAAGGCCATCTCCGGGTCGCTCGCCACGATCCCGGTGCGGCTGAACGCCAAGCAGGCGGCCCCGGGTGCCGCGTTCGTGAACCGGCTCGCCATCCGGTCCTACAACAGCCCCGCGGTGCGCCTGCAGGACGAGAACATCATCAACCTGTCCAAGGACTTCAGCGTCTACCTGTACAGCGCCCTGGCGGCGGAGATCCCCGCCGCGATCGTCCCGGTCGTCGAGGCGGCCTGACTGTGACCGCTGCCGACCTCCAGAAGTACGTAGGCGCCCACGAGGGTGACGCGACCTACGTCGAGTCGTGCTGGGCCGAGGCCGCGAGCCTCGTCGCCCAGTTCGTCGGTGACGCGACGGTGCCCGCTGAGGTCATCCGCCGCGCCACCCTGGAGGTTGGCAGCGAGCTGTACCACCGTCGCAGCGCCCCCAACGGGGTCGCCCAGTTCGCCAGCCTCGATGGCACCGCAGTACGCGTCGCCCGCGACCCGATGGTCGGTGCGTACCCGCTGCTGACCCGGTACGTCGGTGGGGGGTTCGCATGAGCCTGACCGACCACCGCACCACGCTGGCCGCCGCGCTCTCGGGGGCTGGTCTGCAGGTCGAGGCGCACTTGCCCGAACGAATCAACCCTCCGGTCGCGATCCTCACTCCCGGCACCCCGTACCTCGAGGGCGGGGACACCTACGGGTCGTACACGCTGCGGTTCACCGTGCTGCTGGTGACGCCCACCGCGGCGAACGCGACCGCCACCACGGTACTGGACGAGCTGATCGTCAAGGCCGTGGCCGGGGTCGAGGGCGCCGACGGGTTCGGCCTGGAGCGGGTCGACCAGCCCGCGATGCTCCAGGCGAACAACGCCCAGTACATGTCCACGACCGTCGAAGTGCTCAAGCACATCAGGCTCTGAGGGAGGCGCTGTGGGGTCGACCCGGATCAAGTCCAACCGGCTCAGCTTTCGCCTCGGCGACGGCGAGGCCGACTTCTGGGCTGACCTGTCCGAGGTCGTCATGGACGCGGACCGGACCTACGTGCCGCTGCTGGCCGGCGGGTACCGGGCCCGTGAGGAGTGGTTCTTCGACGTCTCGGCGATCCAGTCCACCGCGCCCGGGTCGTTCTGGACGTTCCTGTTCGACCACGCCGGGGAGATGCACCCGTTCGGTTACGCCCCGCACGGCAACCCCATCCCGACCGTGGACGAGCCCCACTTCACGGGGATCGTCCAGATGCCGGCCCGCCCTTCCCTGGGTGGTGCCGCGTCCCCTGACGGCGAGTACAGCTTTGACGCTCGCCTGTTCATCATCTCCGGCCCACTGAGGGTCACCGAGTAAGGAACGGAGGCCCCCTCATGGGCTCTACCCGCATCAAGGGCAACAAGCTCGCACTGAAGTTCGGCTCCCCGGCCGAGGACTTCTGGGCAGACGCGACCAGCGTCGTCCTGGAGAACGAGGAGACCTCCGGCGACGGTGTCATCACCTTCGAGAACGCCGCCCAGGTCGACGACTCCCGGCAGTGGTTCTTCACCCTGTCCGCGATCCAGTCCACCGCCGCCACCAGCTTCTGGCGGTACCTGTGGGACAACACCGGCGAGACGGTGGCGTTCACCTACGCTCCGCACGGCAACGCCGACCCCACCGACAGCGAGCCGCACTTCATCGGCACCTGCAAGATCGGGCCGAAGCCGTCGGTCGGTGGCGAGGCGTCCGCCACGGGGGAGTACACCTTCGAGACCCGCCTCGACGTCGTCACCGGCCCCACGCTGGACGTCGGCGGGGCCTGACCATGGCGGGCGCGGGCGACTTCACCACCGACGGGCCGGTGAAGATCAAAGTCGAGGGGCTGAGGAAGACCGTCCGGGCGATGGAAGCCGCTGGCGCTTCCTCCCAGGACATGAAGGACCTCATGCACGCCCTGGGCCTGATCGTCGTCCGCGCCGCCCAGCCACGCTCACCGATCATCTCCGGCCGCCTGTCCGGTTCGCTGCGGGCCGGTCGGGGCAAGACCAAAGCAGTCGTGCGGGCCGGCGGGGCCCGCGCCCCGTACGCCGGGGTCATCCACTACGGGTGGCCCGCCCGCAACATCGCCGCGCACCCGTTCCTCGCGGACGCGCTGCAAGCCACCCGCTCGCAGATCTTCTCCGCCCTGAACGACGGGCTGGGAGACCTGCTCAAGAAGCACGACCTCACCTGACCACCACACGGAGGAACCATGATCGACATCAACCGCCTCACGCTCGGAGAGATCGCCAAGGTCGAGGAGCTGTCCGGGCAGCCCATCTCCACCATCGGTGACGAGAAGGCACCCAAGGGCCTCGCCCTGGCCGCGCTCGCGTTCGTCGCCAAGCGCCGCGAGGACGCCAAGTTCTCCTGGAACGCCGCCCAGGAACTGACCATCGAGGACGCGAACACCATCCTCGGCCTCGGTCAGGAGGTCACCGACGCCCCTTTGGACGGTGGCTCGGCGAAGCCGGCGAAGACCCGGACGAAGTAGCCCGCCGGTGGGCTGAGGACATGGCCATGTTCGTCGTGCACATGCGCCTCAGCCCCACCGAGTACCGGGCTTTGACCCTGATCGAACGAGACGCCCTGGTGCGCGAGCACAACAAGGCCAACCGCAAGAGGAGGTGACCCGTGGCAGGTCAGACCATCCAGATCTCTGTCCTGGCGGACACCAAGAAGTTCTCCTCCGCGATGCGGGGACTGTCCCAGGAGACGGGTCTGTCCAAGCTCGGGGCCGGGTTCGCCGCCCTCGGCAAGGCTGCTGCTGTCGGGCTCGCCGCCGCCGCGGCGGGCCTCACCGCCCTGGGCGTCAAGGCGGTCGGTGCCGCCGGTGAGCTCGAGCAGTCCATCGGCGCCGTGGACACCGTGTTTAAGGACTCCGCCGGGCAGATCCACGAGTGGGCCAAGGGTGCCGCGGAGGCGGCCGGCCTGACCCGCAACCAGTACAACGAGCTCGGCACGCTGATCGGGACGCAGCTGAAGAATGGCGGCACCGCCATGGATGAGCTCGGCCCGAAGACGAACAACCTCATCACCCTCGGTGCCGACCTGGCGTCCATGTTCGGTGGGACCACCGCTGACGCTGTCGGGGCGCTGTCGTCGGCGCTGAAGGGCGAGCGGGACCCCATCGAGAAGTTCGGGGTGAGCCTGAATCAGGCGGCCATCGACGCCAAGGCCGCGGAGATGGGGTTTGAGAAGGTCGGCGGGGCGCTGTCCGCCGAGGCGAACCAGGCCGCGACCCTGGCGCTGATCATGGACCAGACCGCGGACGCGCACGGCAACTTCGCCAAGGAGTCCAACACCCTGGCCGGTCAGCAGGAACGGCTCAAGGCCAAGCTCGGGAACATCACCGCCACTCTGGGCATGTACCTGCTGCCCATCCTCACGGCGGTGACCGCGTGGGTGTCCGACCGTCTGGGCCCGGCGTTCGAGGCCCTCACCGCCTGGATCGAGACGTCTGCGGTCCCGGCGCTGCAGTCACTGGGCGGCTGGCTGCGGGACAACGTCCTGCCCGCCCTGCAGGACCTGGCCACTTGGGTGCAGGGGACCGTGGTGCCCGCCCTGCAGGCCATGGGTGAGTGGATCACCGGCACCCTCGTCCCGGGCCTGATGGACGCCGGGACGTGGATCAACAACAACAAGGACTGGCTCGCCGCCCTCGCCGTCACCGTGGGCACCATGGTGGTTGCCTACCAGGGGTACGTGCAGGTCATGGCGATCTGGAAGGCCGCCACCGTCGCCGCCCAGGCCGTGCAGGTGGCGTTCAACGCCGTGATGGCCGCGAACCCCATCGGGCTGATCGTCCTGGCCATCGCGGGTCTGGTGGCCGGGCTGGTGTACTTCTTCACCCAGACCGAGACCGGCAAGGCCATCGTCGAGACTGCCTGGGCTGCCATCCAGGGCGCGGTCGAGGCCGTCAAGACGTGGTTCACCGACACCCTCGTGCCGGCCCTGTCGGCGGCGTGGGACACCATCACCTCCGGGCTGTCCACGTTCGCGACGTGGCTGTCGGACACCTGGACGTCGATCAAGAACACCGCCACCGACAAGTGGAACGGCGTCCTGGACTTCTTCCGGGGCATCCCCGGCAAGGTCACCGACTTCTTCATGAACTGGACTCTCCTGGGGCTGCTGATCCAGCATTGGGACTCCATCAAGACCACCGCCACCGAGAAGTGGAACGCCCTGGTCGACTGGGTCAAGGGCATCCCGCAGCGGTTCGTAGACGGGCTCGCCGCGATCGCGAACATCGCGATCCAGATCGGTATCTGGGTGCTCGGCATTAAGGACGCTGCGGTAGAGAAGTTCATGCAGCTCGTCGACTGGGTCAAGGAGCTGCCCGGGAAAATCCTGTCCGGCCTCGGTGACCTCAGCCGCCTGCTGATCAACGCGGGCAAGAACATTATCGAGGGGCTGTGGAACGGGCTGAAGGCGAAGTGGGAGGCGGTCAAGGACTGGGTCGGCGGCATCGCTGACTGGATCGCCGACAACAAGGGCCCGAAGGCGTACGACCTGAACCTGCTGGTCAACGCGGGTAAGTGGATCATGCAGGGCCTGCAGGACGGTCTCCGGTCGGAGATCCCGAACCTGCGCCGCACCTTGGAGGGCGTGTCCGCTGAGGTCGCCAGGACCCCCATGGCGCCCCTGCAGGTGGGCACGTCGGCGTCGTCCACGTCGGCGAGCCGGTGGGGCGCGGCGGGGTCGAACACCAACCCGGCCATGGACGGCGGGCACACCACCGCACCGCTGGACCTGTCCGAGAAGTCCATCCGAGGCATCGCTGACGCGGTCCTCGCGGGGGCGGGGGCTGTCGGCACCGCGTCCGCCCGGGAGCAACTGAACCACGCAAGGCGAGGAGTGAGGCGGTAA

Protein sequences of DBSCAN-SWA_2

>NZ_CP040915|2072352:2083359|2073938_2074190_+|WP_139928479.1|DBSCAN-SWA
MSKHSSAGSAWQAIRLRILQRDGYTCAYCGREADTVDHIVAKANGGTDDESNLIAACRTCNGYKQDRQQIRVPYVNTKWLTSV
>NZ_CP040915|2072352:2083359|2074565_2076008_+|WP_139928483.1|DBSCAN-SWA
MVFAPALMTPPLSEDFTTDGDWLLRFADLAWCTPESPAGIELDAWQRELLRRMLETYPPGHERAGELRYRQVLVSLGRQNGKSVIGALLGLYGLLRAPGALVIGVASTAEQARIIYDRTMFVINQNPTLKRRFERLTDTRGIQAKDGSKYEIKAAKSAAVQGLPVSLGLFDELHIAREEVWQALVNGTGGRKDGIVVGITTAGDDESALLKGLYDLAKRAAGGEATLERFGAFIWEAPASRVPEDDGELLEFLKAANPALADGRLDAQNLISDIRAMPEPDVIRYRLNRFLDSSAASFLSQDQWVAAGRGDGETFPEGRPVFAVDRSPDWGFATVTANVKVDGVTHTEVVASLVNPTLERLLQVCTQLSVHSPSMFVMDGYALRDLGGELKRRGLQVRICTQGDVVNASSLFYSKVVRRELRHGNDGLLSVQIPRTVRRNVGEAFRISRKDSSVEIDAVLATALGVWAAEVETDVPVQIF
>NZ_CP040915|2072352:2083359|2072352_2072811_+|WP_139928475.1|DBSCAN-SWA
MKPSEAAKVLTYVAAFNGRTVGKTDAMAWADALHPDVTYEDAKTAVAQHFAESTDWCMPAHINQRVKTIWRERVDAIGGAVPPPPDSIADRPGHCYSEWHQVFLRAVKIGATPEEADQQACAAVQITRAPNDPLRSLSWRRAQREQQQLGAA
>NZ_CP040915|2072352:2083359|2079032_2079401_+|WP_139928491.1|DBSCAN-SWA
MSLTDHRTTLAAALSGAGLQVEAHLPERINPPVAILTPGTPYLEGGDTYGSYTLRFTVLLVTPTAANATATTVLDELIVKAVAGVEGADGFGLERVDQPAMLQANNAQYMSTTVEVLKHIRL
>NZ_CP040915|2072352:2083359|2076263_2077214_+|WP_168205649.1|portal|DBSCAN-SWA
MSILATGVSQLTVDVWRGDEPSPRVPAWVRRPDIKVSRSAFFEQTTVGLAVTGNAFWRVHRDSAADPVQALTVLNPHDVVINEDGTYGYQNQRPLQDWQVQHLALLRVPGARYGLGPIQAARADLAGVLDLRDYAAEWFNTAGVPNGVLSTEQVLAPDQAAQYKKQWMEQQSHKNGPAVLGAGIAYSPIMLSPKDAQFLESRRYTVTEIARLFGIPASLMLATVDGAAMTYQNVADADLSFARWTLVQYLREIEEAISTLLPRGTEARFNLDAVLRPSTKARYDAHKIAIEAGFLTVDEVRAIEGLKPLPMREPHR
>NZ_CP040915|2072352:2083359|2074316_2074565_+|WP_139928481.1|DBSCAN-SWA
MAARTFVSSLRSFQKASPWLGPEHDPALVMLEAMAKELDGGELTPALLSQFGLAYRSLQKLAPRSDRGEVDPLDEVLAERGR
>NZ_CP040915|2072352:2083359|2081121_2083359_+|WP_139928500.1|DBSCAN-SWA
MAGQTIQISVLADTKKFSSAMRGLSQETGLSKLGAGFAALGKAAAVGLAAAAAGLTALGVKAVGAAGELEQSIGAVDTVFKDSAGQIHEWAKGAAEAAGLTRNQYNELGTLIGTQLKNGGTAMDELGPKTNNLITLGADLASMFGGTTADAVGALSSALKGERDPIEKFGVSLNQAAIDAKAAEMGFEKVGGALSAEANQAATLALIMDQTADAHGNFAKESNTLAGQQERLKAKLGNITATLGMYLLPILTAVTAWVSDRLGPAFEALTAWIETSAVPALQSLGGWLRDNVLPALQDLATWVQGTVVPALQAMGEWITGTLVPGLMDAGTWINNNKDWLAALAVTVGTMVVAYQGYVQVMAIWKAATVAAQAVQVAFNAVMAANPIGLIVLAIAGLVAGLVYFFTQTETGKAIVETAWAAIQGAVEAVKTWFTDTLVPALSAAWDTITSGLSTFATWLSDTWTSIKNTATDKWNGVLDFFRGIPGKVTDFFMNWTLLGLLIQHWDSIKTTATEKWNALVDWVKGIPQRFVDGLAAIANIAIQIGIWVLGIKDAAVEKFMQLVDWVKELPGKILSGLGDLSRLLINAGKNIIEGLWNGLKAKWEAVKDWVGGIADWIADNKGPKAYDLNLLVNAGKWIMQGLQDGLRSEIPNLRRTLEGVSAEVARTPMAPLQVGTSASSTSASRWGAAGSNTNPAMDGGHTTAPLDLSEKSIRGIADAVLAGAGAVGTASAREQLNHARRGVRR
>NZ_CP040915|2072352:2083359|2080699_2080981_+|WP_139928498.1|DBSCAN-SWA
MIDINRLTLGEIAKVEELSGQPISTIGDEKAPKGLALAALAFVAKRREDAKFSWNAAQELTIEDANTILGLGQEVTDAPLDGGSAKPAKTRTK
>NZ_CP040915|2072352:2083359|2079839_2080271_+|WP_139928495.1|DBSCAN-SWA
MGSTRIKGNKLALKFGSPAEDFWADATSVVLENEETSGDGVITFENAAQVDDSRQWFFTLSAIQSTAATSFWRYLWDNTGETVAFTYAPHGNADPTDSEPHFIGTCKIGPKPSVGGEASATGEYTFETRLDVVTGPTLDVGGA
>NZ_CP040915|2072352:2083359|2077210_2078731_+|WP_139928487.1|DBSCAN-SWA
MSEELLTREATFTASDVEAREVVGIAVPWEQPTDLAGYREQFARGSVVDSDEALLFYGHAEPIGRVIRAEDTDAGWEITARISETARGDEVLTLLRDEVLTKFSVGFRPVEARTEEDGLVTRTKVNVREVSVVPFPAYAGASISEVRERPSDEAHQRQEGADMPDNVTAADLEQVRASIEDLDREVRMIQTDKPTEPVVDTRSAGEVLKAIASGDEAELRAYTGGTTADTVAKNGWVGDLTRLVDEAATLRGLFSTGNLPAEGNFIEYAVLGENTAVVGDQGGEGKDLPYGKVTVTTATAPVKTYGGYTQLTRQEIERSSVAILDHNLRAQSIATGKALNAAFRTFYAAQVAAQTSAGNTVEIPAAADYTDWLGAVVDAAEKYEDLGVSLDALVVDKTIFKTLLGFTGSDGRPMMSVDGSGANTVGSLDVKAISGSLATIPVRLNAKQAAPGAAFVNRLAIRSYNSPAVRLQDENIINLSKDFSVYLYSALAAEIPAAIVPVVEAA
>NZ_CP040915|2072352:2083359|2080273_2080681_+|WP_139928497.1|DBSCAN-SWA
MAGAGDFTTDGPVKIKVEGLRKTVRAMEAAGASSQDMKDLMHALGLIVVRAAQPRSPIISGRLSGSLRAGRGKTKAVVRAGGARAPYAGVIHYGWPARNIAAHPFLADALQATRSQIFSALNDGLGDLLKKHDLT
>NZ_CP040915|2072352:2083359|2072810_2073740_+|WP_139928477.1|DBSCAN-SWA
MSRRHDPRALDTPERSEGAWEYETWAAQWGDTETTTPPADWQVAWADTTISTVEKVWSEQGAKLYAPHRYKWLRDDLHTWLLIEAQKVADWYVPVPCPDPEGMWAATLWRTLRKSARWHFGTVAKTVEEQDAYHRGVTSTNYLTAEVGDAWLPRHAIHGDDWTSRDPADVVGRVEALAEKVRQAETYTREQGSTYTTETSPYCSEPLCTQPVDINGQCRPHYEKERRLWGNVNGRLCNIPGCGRPHRSRGLCNTHQAQLRGGRLPAEYMQYAEAKQQPATGCQVPGCDRPHDARGYCAKHYAIWRKGTL
>NZ_CP040915|2072352:2083359|2079411_2079822_+|WP_139928493.1|DBSCAN-SWA
MGSTRIKSNRLSFRLGDGEADFWADLSEVVMDADRTYVPLLAGGYRAREEWFFDVSAIQSTAPGSFWTFLFDHAGEMHPFGYAPHGNPIPTVDEPHFTGIVQMPARPSLGGAASPDGEYSFDARLFIISGPLRVTE
>NZ_CP040915|2072352:2083359|2078733_2079036_+|WP_139928489.1|DBSCAN-SWA
MTAADLQKYVGAHEGDATYVESCWAEAASLVAQFVGDATVPAEVIRRATLEVGSELYHRRSAPNGVAQFASLDGTAVRVARDPMVGAYPLLTRYVGGGFA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_139928475.1|2072352_2072811_+	hypothetical protein	I4AZL1	Saccharomonospora_phage	1.7e-08	36.0
WP_139928477.1|2072810_2073740_+	hypothetical protein	NA	NA	NA	NA
WP_139928479.1|2073938_2074190_+	HNH endonuclease	A0A1B5FP94	Escherichia_phage	2.1e-10	48.7
WP_139928481.1|2074316_2074565_+	hypothetical protein	NA	NA	NA	NA
WP_139928483.1|2074565_2076008_+	hypothetical protein	A0A2R3ZZF5	Microbacterium_phage	6.8e-117	48.3
WP_168205649.1|2076263_2077214_+|portal	phage portal protein	A0A2R4A099	Microbacterium_phage	3.5e-77	49.8
WP_139928487.1|2077210_2078731_+	hypothetical protein	A0A2R4A075	Microbacterium_phage	1.1e-101	44.0
WP_139928489.1|2078733_2079036_+	hypothetical protein	A0A2R3ZZF6	Microbacterium_phage	5.4e-16	54.7
WP_139928491.1|2079032_2079401_+	hypothetical protein	NA	NA	NA	NA
WP_139928493.1|2079411_2079822_+	hypothetical protein	NA	NA	NA	NA
WP_139928495.1|2079839_2080271_+	hypothetical protein	A0A2R3ZZJ6	Microbacterium_phage	6.5e-31	51.7
WP_139928497.1|2080273_2080681_+	HK97 gp10 family phage protein	A0A2P1CBZ9	Gordonia_phage	1.8e-14	36.4
WP_139928498.1|2080699_2080981_+	hypothetical protein	A0A2R3ZZH0	Microbacterium_phage	6.5e-08	40.7
WP_139928500.1|2081121_2083359_+	hypothetical protein	A0A2R3ZZQ3	Microbacterium_phage	2.7e-48	54.2

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP040915|3416932:3423215|DBSCAN-SWA
GATGACCAGCTGGCTGCAAGGACCGCTCCTCGGGTTCGACACCGAGACCACCGGCGTCGACGTCGCCACCGACAGGGTTGTCAGCGCGGCGCTCGTGCGGCGCGACGGCGCGGGCTCGACGACGCGCACGTGGCTCCTCGACCCGGGGGTGGACATCCCCGCCGGCGCGACGGCGATCAACGGCATCACCACCGAGCACGCCCGCACCCACGGGGCGGCGCCGTCCACCGCGCTGGAGGAGATCGCCGCGGAGATTGCGGCGGCGCAGGCGGCCGGGGTGCCGCTGGTCGCCTACAACGCCGCGTACGACCTCGCGCTCCTCGAGCACGAGCTCGCCCGGCACGCGCTGCCCGGCCTGGCCGAGCGCCTGTCCGGCGGCCTGCTGGTCCTCGACCCGCTGGTTCTCGACCGGCACGTCGACGGCTCGCGCCGCGGCCCGCGCAAGCTCGTCGACCTGTGCGAGGTGTATCTCGTACCGACCGGCGAGCTGCACACCGCCGAGGTCGACGTCGTCGCGACCTTGGACCTGCTCGCCCAGATGGCCGGCCGCCACCCGCAGCTCGTCGCGGCCACGCCCAACCAGCTGCACGCCACGCAGGTGGCCGCGCACGAGGAGTGGGCACGGTCGTACAACCGGTGGCGCGCCCGGCGGGGCCTGTCGTGGCCGGGCGCCGACCGCGGCTGGCCCCTGCCCGAGGAGCCGTCGCGCGGGGCGCTGCTGGTCCGCCGTCTGGTCTGGGCCGCCCACTGGGTGGCCGGCGTGCCGCACCGTCTGGTGCGGCGCCGCCGTCAGCGGCGCGAGGAGTAGTTCGGCGCCTCGATCGTCATCTGGATGTCGTGCGGGTGGGACTCCTTCAGGCCCGCCGAGGTGATGCGCACGAACTTGCCGCGCTGCTGCAGCTCGGGGATGGTCCGCGCACCGACGTAGAACATCGACTGGTGCAGGCCGCCCACGAGCTGGTAGGCGACGTTGGACAGCGGGCCGCGGTAGGGCACCTGGCCCTCGATGCCCTCGGGGACGATCTTGTCGTCGGTGTCGACGTCGGCCTGGAAGTACCGGTCCTTGGAGTACGAGACCCGGCCGCGGGAGGCCATGGCGCCCAGCGAGCCCATGCCGCGGTAGTGCTTGTACTGCTTGCCGTTGACGAAGACCAGCTCGCCGGGGGACTCCTCGCAGCCGGCGAGCAGGGAACCCAGCATGACGGTGTCCGCCCCGGCGACCAGCGCCTTGGCGATGTCGCCGGAGTACTGCAGTCCGCCGTCGGCGATGACCGGGACACCGGCCGGCTTGCAGGCCTGGGCGGCGAGGTGGACGGCGGTGACCTGCGGGACGCCTACGCCGGCGACCACGCGGGTGGTGCAGATCGAGCCCGGGCCCACGCCGACCTTGACGGCGTCCACACCGGCGTCCACGAGGGCCTGCGCCCCTTCGCGGGTGGCGACGTTGCCGCCGATGATCTGCACGTGCGCGAAGGCCTTGTCCTTCTTCATCTTCGCGATCATGTCGAGCAGGAGCTTCGCCTCGCCGTTGGCGGTGTCGGCCACGAGGACGTCGGCGCCGGCCTCGGCGAGCGCGGCGGCCCGCTCCCAGGCGTCGCCCCAGTAACCGATGGCGGCGCCCACCATGAGGCGCCCCTCGGCGTCCTTGGTGGCGTCGGGGTACTGCTCGGACTTGACGAAGTCCTTGACGGTGATGAGGCCGCGCAGCTTGCCCGCGTCGTCCACCAGCGGCAGCTTCTCGATCTTGTGCTGGGCGAGCAGGGCGGCGGCGTCCGGCGAGCTGATCCCCACCGGGGCGGTGATCAGCGGCATCGGGGTCATCGAGTCGCGCACGGTGCGGGTGTCGAACTCCGCGGGCGGGATGAACCGCAGGTCGCGGTTGGTGATGATGCCGAGCAGCACGCCGTCGGCGTCCACGACCGGCAGGCCGGAGACGCGGTAGCGCCCGCACAGGGCGTCGAGCTCGGCGAGCGAGGCCTCCGGGCCCACGGTCACGGGGTCGGTGACCATGCCGGACTCCGAGCGCTTGACCACGGTGACCTGCTGCGCCTGCTCCGCGATGGAGAGGTTGCGGTGCAGGATGCCGATGCCGCCCTGGCGGGCCATGGCGATCGCCATCCGCGCCTCGGTGACGGTGTCCATCGCGGCCGAGACCAGCGGCACCCGCAGGCTGATCTCCTTCGTCAGCCGCGAGGCGGTGCTCACCTCGGAGGGGATGACGTCGGTGGCGCCAGGCAGGAGCAGCACGTCGTCATAGGTCAGGCCGACCAGGGCAAACGGGTCATTGATGTGCGTCTCGGTCACACGGTGATAGTACGTGCGCCGGAGGCCCCGGAGCATAAGGGGTGACGCGTTCCACGCCCGCCCGCCCTCACTCGTCCACGAGGCGGGGCCTCACTCCTCCATGAGGCCGGCGATCTCCTCCACGGCGGCCAGCGCGCTGCGCACCCGGTGCACCCGGGGCAGCCACAGGTCCGGGGCGTCGCCGCCGAGCAGGAACACCTCGACGTCTCCGCGGGCCGAGACCGCGCGGACCAGCTCGTCGGTGCCGGGCGGGTTCCCGACGACGGCGAGCACGCGCGCCGCACGCTCGGCGATCGTCCGCAGCCCCTGCTCCGGCCCGCCCAGGCTCTCGGCGCGCAGGACGCGCGCGCGGACCCCGCGCTCGGCAAGACCGCCGCCGATGACGTGGGCGCGCAGCCGGCGGTCCTGCGCCGCGCAGAGCAGCGCGGTGCGGCTGGCCGAGGCGGTGGGGCCGTCGCCGGGGCGCAGCAGGTGCACGCCGCTCTCGCGGGCCCGTTCAGCTGCCGTCGCGACCTCGCGGACTGCGGTGAGGACGGCGGTGGCGATGACGCCCTCGGGGTCCACGCCGGGGCGGTCGGAACGCTCCCGCTGGGACAGCATCGCCAGCGCTGGCTTGGCGAGGCTGGTCCAGGCCTTGACGATGCCGGCGTCGCGGACCTCCTGGTCGAGCATCCGGTGCACGCGCGGCGCGTCCGGCTCGAGCGCGGCGGCGGCGAGGGAGAGCGGGTCGACGAGCAACCGCTCGTGGTGTGCGGGCTCCTCGGCCGCGGACTCCTGCAGCCGCCTGGGCCACGGGTGGGCCTCGAGGGGGACCGCGGGGTCCGAGCTGAGGGCGGCGCGGGCGGCGTCGGAGGGGGCGACCCCCTGCAGGGTGAGATGACGCATCCGCTCGAGCCGGGCGACGTCGGCGGGGGTGTAGCGCCGATGGCTGCCGGCCTCGTGCGAGGACGGTCCCAGCCCGTAGCGCCGGTCCCACGTGCGCAGGGTCGAGGCGGCGACCCCGAGCCTGGCCGCGACGGCGGCCACGGTCAGCGGAGCACCGCCCTCGCCGTCCGGCGAGGGCCGCCTCCGGGACCCGTCGCGGCCCGATGGCCCGGGAGGACGGCCGGATCCACGCGCGGACGCAGCCATGCCCGTCACCGCACTCCCTTCGTTGCCATGGATCGATCTTGACGCGATTTCGCCCATCTCGCCACCGCGCCGCTCCGACGACGGACGGAAAGTGACCGAATGACCAACTTTCGCGAGGGTCTTGAACAAGTTGTGCATCGGTTGCTAGTTTCTCTGACAGGGGGAACTCCCCCGGGGGGAGTTCCCACCGCAGGCAGACCTACGGAAGGACGATGAAGATGGCAGAGCTCTCGAGGCTTCCGGGCCCGGTGATGGATCTGTGGGAATGGCAGTACCAGGGGAAGTGCCGCGAGGCGGACCCCAACCTCTTCTTCCACCCCGAAGGTGAGCGGGGTGGCACACGCCGTCGCAGGGACGAGGCGGCGAAGGCGATCTGCGCCACGTGCCCGGTGATCGAGCAGTGCCGCTCGCACGCGTTGCGGGTGCGTGAGCCGTACGGCGTCTGGGGCGGCCTGAGCGAGGACGACCGTCAGGCGATCCTCGCCCGCCCGGCACGTCGCGCGTCCTGACGGCGCTGCCTGCGGACGACGGAGCTGCGCGGCCACGGTGGACGCCACGCAGCCCCGGACCTCACGAGGAGGTCCGGGGCTGCGTGGTGCCGGCTAGGCGGCGGTCACTTCTCGACGACGGCGAGGATGTCGCGCGCGGAGAGGATCAGGTACTCCTCACCCGCGTACTTCACCTCCGTGCCGCCGTACTTGCTGTAGATGACGACGTCGCCGACGGCGACGTCGAGCGGAACCCGGTTGCCGTTGTCGTCGATGCGACCCGGGCCGACCGCCAGGACGGTGCCCTCCTGGGGCTTCTCCTTGGCGGTGTCCGGGATGACCAGACCGGAAGCCGTGGTCTGCTCGGCCTCGAGGGTCTGAACGACGATACGGTCCTCGAGCGGCTTGATGGAGACCGACACTGCGGACCTCCCCTTCGCGTGTGTGATGGGACAGTACATAGGGTTTCGCGCACCCTCCGCTCCGCACCCGCCGTCGCGGGGGTCGGGCGCCGAGCATCCGGTACGCCGCCGCGACCCCGAAGGGCCGCGCCTGGCCCTCAATCTAGGACCGGAATTAGCACTCGGTCAAGGTGAGTGCCAATGCGTGGCCGGGGCAGCGCGCCCACCGCCGCCGCGCACGCACCACAGCGGCGCTGTCAGACCGCGCCGGAGATCCGCGGGACAGCGGCGACAAGCTGGGCCGTGTACGGGTGCGCCGGCTGGTCGAGCACCTGCCGGGTGGCCCCGGTCTCGGTCAGCCGGCCGTCCTTGAGCACCGCCGTCCGCTCGCACACCGCGGCGATGACGCTCATGTCGTGCGAGACCATCACGATCGTCAGGCCGTGCTCGCGCTTGAGCCGGTCGAGGAGGGCGATGACGCCCAGCCGGGTGCTGACGTCGAGCGCGCTCACCGGCTCGTCGGCGAGCAGGACACGGGGCCCGGTCACGAGCGCACGGGCGATGGCGATGCGCTGGCGCTGGCCGCCGGAGAACTCGTGCGGGAACCGGGAGGCGACGTCGGGCTCGAGGTCCACCGCCGCAAGGGCGCGCGCGACCGCGTCACGCGCCTCCCCCGCACGCTTCACACGCAGCGAGACCAGGGGCTCCGCGACGATCCGGTCCACCCGCTGGCGTGGATCGAGGGAGGAGTACGGATCCTGAAAGACCACCTGCACCTGGCGCCGGAAGCTGCGCATCCGCCGGCGGTCCGCCGAGTCGAGGCGCTCCCCCTCGAACAGCACACGTCCCGCGGTGGGCCGTGCCAGGCCGAGCAGGAGGGACAGTGCCGTGGACTTTCCCGAGCCGGACTCGCCCACGATGCCCAGGCTTACGCCGTCGTCGACGGCGAGGGTCACCTCGCTCAGCGCGTTCTCGGAGGCGCCGCGGTAACGGAAGTCCACCGCGTCCAGGGCCAGGACCGCGCTCATCGCTCCGGGCTCCCGTCGCCGCCCAGTGGTCCGCCCACGGGGCCGGTGACGGCGCTCGGGCTCCACGTGCCCGCGAGCGCGGCATCCAGCAGCCTGGCCCCCTCGACCAGACGCTGGGTGTACGGGTGCTGCGGCGCCGCGATCGTGCCGGCCACACTGCCCTCCTCGACCTTCCGCCCCGAGCGCAGCACCACCACCCGCTCGGCGACCTCGGCGACGACGCCCATGTCGTGGGTGATGAAGACCAGCGCCATGTCGCGCTCGCGCACCTCGCGCTGCAGCAGCTCGAGGATCCCCGCCTGCACCGTGACGTCCAGCGCGGTGGTGGGCTCGTCGGCGATGAGCACCTTGGGGTCGCAGGCCAGGGCCATGGCGATGGCCACGCGCTGGCGCTGCCCGCCGGAGACCTCGTGCGGGAACGCCTGCTCCGCCCGCTCGGGCAGCGCCACCTCCCGCATCAGCCCGCGCACGCCGTCGCGCAGCTCCGTCCCGCGCAGCCCACGGTGGCGCCGCAGCGGCTCGGCGATCTGCCGGCCGATCCGCATGAGCGGGTCCAGCGCGGTGCGCGGCTCCTGGAACACCAGGCTCACCCCGGCGCCGCGCACACGATTGAGCACCGCCTCCGGAGCTCCGACCACCTCGCGGCCCGCCACCGACACCGAGCCGCTGGCCTGCAGGCCGGGCGCCAGCAGACCCGCGACCGCGAGCGCCGTCAGCGACTTGCCCGAGCCAGACTCGCCGATGATGGCCAGCCGCTCCCCCGCCGCGACGGTGAACGAGAGGTCGTCGACCAGGCGCCGGGCAGGCTCGCCGGCCCGGCGGGCGCCAGCGGCACCGCGGGCGCCAGTGGCGCCCCGGGCCCCGGCGGCGCCTCGGGCCTCCCCCGCGAGGACGGTGAGCCCGGCCACGCTCAGCACGGGTGCCGCGGTCAT

Protein sequences of DBSCAN-SWA_3

>NZ_CP040915|3416932:3423215|3422279_3423215_-|WP_139930074.1|DBSCAN-SWA
MTAAPVLSVAGLTVLAGEARGAAGARGATGARGAAGARRAGEPARRLVDDLSFTVAAGERLAIIGESGSGKSLTALAVAGLLAPGLQASGSVSVAGREVVGAPEAVLNRVRGAGVSLVFQEPRTALDPLMRIGRQIAEPLRRHRGLRGTELRDGVRGLMREVALPERAEQAFPHEVSGGQRQRVAIAMALACDPKVLIADEPTTALDVTVQAGILELLQREVRERDMALVFITHDMGVVAEVAERVVVLRSGRKVEEGSVAGTIAAPQHPYTQRLVEGARLLDAALAGTWSPSAVTGPVGGPLGGDGSPER
>NZ_CP040915|3416932:3423215|3421512_3422283_-|WP_139930073.1|DBSCAN-SWA
MSAVLALDAVDFRYRGASENALSEVTLAVDDGVSLGIVGESGSGKSTALSLLLGLARPTAGRVLFEGERLDSADRRRMRSFRRQVQVVFQDPYSSLDPRQRVDRIVAEPLVSLRVKRAGEARDAVARALAAVDLEPDVASRFPHEFSGGQRQRIAIARALVTGPRVLLADEPVSALDVSTRLGVIALLDRLKREHGLTIVMVSHDMSVIAAVCERTAVLKDGRLTETGATRQVLDQPAHPYTAQLVAAVPRISGAV
>NZ_CP040915|3416932:3423215|3419325_3420261_-|WP_168205720.1|DBSCAN-SWA
MAAVAARLGVAASTLRTWDRRYGLGPSSHEAGSHRRYTPADVARLERMRHLTLQGVAPSDAARAALSSDPAVPLEAHPWPRRLQESAAEEPAHHERLLVDPLSLAAAALEPDAPRVHRMLDQEVRDAGIVKAWTSLAKPALAMLSQRERSDRPGVDPEGVIATAVLTAVREVATAAERARESGVHLLRPGDGPTASASRTALLCAAQDRRLRAHVIGGGLAERGVRARVLRAESLGGPEQGLRTIAERAARVLAVVGNPPGTDELVRAVSARGDVEVFLLGGDAPDLWLPRVHRVRSALAAVEEIAGLMEE
>NZ_CP040915|3416932:3423215|3417720_3419271_-|WP_139930069.1|DBSCAN-SWA
MLRGLRRTYYHRVTETHINDPFALVGLTYDDVLLLPGATDVIPSEVSTASRLTKEISLRVPLVSAAMDTVTEARMAIAMARQGGIGILHRNLSIAEQAQQVTVVKRSESGMVTDPVTVGPEASLAELDALCGRYRVSGLPVVDADGVLLGIITNRDLRFIPPAEFDTRTVRDSMTPMPLITAPVGISSPDAAALLAQHKIEKLPLVDDAGKLRGLITVKDFVKSEQYPDATKDAEGRLMVGAAIGYWGDAWERAAALAEAGADVLVADTANGEAKLLLDMIAKMKKDKAFAHVQIIGGNVATREGAQALVDAGVDAVKVGVGPGSICTTRVVAGVGVPQVTAVHLAAQACKPAGVPVIADGGLQYSGDIAKALVAGADTVMLGSLLAGCEESPGELVFVNGKQYKHYRGMGSLGAMASRGRVSYSKDRYFQADVDTDDKIVPEGIEGQVPYRGPLSNVAYQLVGGLHQSMFYVGARTIPELQQRGKFVRITSAGLKESHPHDIQMTIEAPNYSSRR
>NZ_CP040915|3416932:3423215|3416932_3417739_+|WP_139930068.1|DBSCAN-SWA
MTSWLQGPLLGFDTETTGVDVATDRVVSAALVRRDGAGSTTRTWLLDPGVDIPAGATAINGITTEHARTHGAAPSTALEEIAAEIAAAQAAGVPLVAYNAAYDLALLEHELARHALPGLAERLSGGLLVLDPLVLDRHVDGSRRGPRKLVDLCEVYLVPTGELHTAEVDVVATLDLLAQMAGRHPQLVAATPNQLHATQVAAHEEWARSYNRWRARRGLSWPGADRGWPLPEEPSRGALLVRRLVWAAHWVAGVPHRLVRRRRQRREE
>NZ_CP040915|3416932:3423215|3420979_3421315_-|WP_139930072.1|DBSCAN-SWA
MYCPITHAKGRSAVSVSIKPLEDRIVVQTLEAEQTTASGLVIPDTAKEKPQEGTVLAVGPGRIDDNGNRVPLDVAVGDVVIYSKYGGTEVKYAGEEYLILSARDILAVVEK
>NZ_CP040915|3416932:3423215|3420584_3420875_+|WP_139930071.1|DBSCAN-SWA
MAELSRLPGPVMDLWEWQYQGKCREADPNLFFHPEGERGGTRRRRDEAAKAICATCPVIEQCRSHALRVREPYGVWGGLSEDDRQAILARPARRAS

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_139930068.1|3416932_3417739_+	DNA polymerase III subunit epsilon	I4AZL6	Saccharomonospora_phage	4.3e-36	42.7
WP_139930069.1|3417720_3419271_-	IMP dehydrogenase	A0A1V0SHK8	Klosneuvirus	1.5e-90	39.5
WP_168205720.1|3419325_3420261_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_139930071.1|3420584_3420875_+	WhiB family transcriptional regulator	I6XD27	Mycobacterium_virus	4.5e-12	46.9
WP_139930072.1|3420979_3421315_-	co-chaperone GroES	A0A221S4M3	uncultured_virus	3.1e-20	52.6
WP_139930073.1|3421512_3422283_-	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	1.1e-15	32.2
WP_139930074.1|3422279_3423215_-	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	2.6e-16	31.5