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_CP040429	Stenotrophomonas maltophilia strain U5 chromosome, complete genome	13 crisprs	DEDDh,csa3,WYL,cas3,DinG,PD-DExK	0	3	3	0

1. NZ_CP040429

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP040429_1

• CRISPR_ID: NZ_CP040429_1
• CRISPR_location: 41506-41606
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_1

Consensus_repeat	Method
GCCCGGCGGAACGCAATCAGGACGCCTCGGT	CRISPRCasFinder

spacers of NZ_CP040429_1

>1.1|41537|39|NZ_CP040429|CRISPRCasFinder
TGAATCGGTTGGGCACAAGCCCTGGTAGCGCCGGGCATG

CRISPR arrays and Neighbor proteins around NZ_CP040429_1

CRISPR arrays

The CRISPR arrays of NZ_CP040429_1

>merge|NZ_CP040429|1|41506-41606|CRISPRCasFinder
GCCCGGCGGAACGCAATCAGGACGCCTCGGTTGAATCGGTTGGGCACAAGCCCTGGTAGCGCCGGGCATGGCCCGGCGCAACGCAATCAGGACGCCTCGGT

>NZ_CP040429|1|1|41506-41606|CRISPRCasFinder
GCCCGGCGGAACGCAATCAGGACGCCTCGGT	TGAATCGGTTGGGCACAAGCCCTGGTAGCGCCGGGCATG
GCCCGGCGCAACGCAATCAGGACGCCTCGGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_025875513.1|28039_29068_-|alcohol-dehydrogenase-AdhP	unknown	unknown	gnl|CDD|176257
NZ_CP040429.1|WP_154878936.1|48710_50300_+|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350116
NZ_CP040429.1|WP_154878930.1|42230_43853_-|carboxylesterase-family-protein	unknown	unknown	gnl|CDD|225181
NZ_CP040429.1|WP_154878926.1|32796_33435_-|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	unknown	unknown	gnl|CDD|235577
NZ_CP040429.1|WP_154878932.1|43849_44833_-|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl|CDD|223730
NZ_CP040429.1|WP_025875485.1|50338_51397_+|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380487
NZ_CP040429.1|WP_154878921.1|29142_30672_-|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|143434
NZ_CP040429.1|WP_059063074.1|34726_37489_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|273804
NZ_CP040429.1|WP_025875515.1|27544_27934_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_032978442.1|51639_52488_+|5-dehydro-4-deoxy-D-glucuronate-isomerase	unknown	unknown	gnl|CDD|179169
NZ_CP040429.1|WP_154878923.1|30717_32745_+|GAF-domain-containing-protein	unknown	unknown	gnl|CDD|225822
NZ_CP040429.1|WP_025875493.1|45857_46862_+|TRAP-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270389
NZ_CP040429.1|WP_154878918.1|24841_27319_+|DNA-ligase-D	unknown	unknown	gnl|CDD|235658
NZ_CP040429.1|WP_134831779.1|46872_47406_+|TRAP-transporter-small-permease	unknown	unknown	gnl|CDD|225632
NZ_CP040429.1|WP_099786335.1|33421_34441_-|sugar-kinase	unknown	unknown	gnl|CDD|238571
NZ_CP040429.1|WP_025875489.1|47409_48693_+|TRAP-transporter-large-permease	unknown	unknown	gnl|CDD|224509
NZ_CP040429.1|WP_154878928.1|37625_41429_+|LamG-domain-containing-protein	unknown	unknown	gnl|CDD|379155
NZ_CP040429.1|WP_154878939.1|52570_53326_+|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD	unknown	unknown	gnl|CDD|188170
NZ_CP040429.1|WP_025875519.1|23911_24838_+|Ku-protein	unknown	unknown	gnl|CDD|238408
NZ_CP040429.1|WP_154878934.1|44990_45818_+|2-keto-4-pentenoate-hydratase	unknown	unknown	gnl|CDD|226480

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_025875513.1|28039_29068_-|alcohol-dehydrogenase-AdhP	gnl|CDD|176257	cd08297, CAD3, Cinnamyl alcohol dehydrogenases (CAD). These alcohol dehydrogenases are related to the cinnamyl alcohol dehydrogenases (CAD), members of the medium chain dehydrogenase/reductase family. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Cinnamyl alcohol dehydrogenases (CAD) reduce cinnamaldehydes to cinnamyl alcohols in the last step of monolignal metabolism in plant cells walls. CAD binds 2 zinc ions and is NADPH- dependent. CAD family members are also found in non-plant species, e.g. in yeast where they have an aldehyde reductase activity. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P) binding-Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	0
NZ_CP040429.1|WP_154878936.1|48710_50300_+|family-43-glycosylhydrolase	gnl|CDD|350116	cd09002, GH43_XYL-like, Glycosyl hydrolase family 43, beta-D-xylosidase (uncharacterized). This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have been annotated as having beta-1,4-xylosidase (beta-D-xylosidase;xylan 1,4-beta-xylosidase; EC 3.2.1.37) activity. They are part of an array of hemicellulases that are involved in the final breakdown of plant cell-wall whereby they degrade xylan. They hydrolyze beta-1,4 glycosidic bonds between two xylose units in short xylooligosaccharides. These are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	0
NZ_CP040429.1|WP_154878930.1|42230_43853_-|carboxylesterase-family-protein	gnl|CDD|225181	COG2272, PnbA, Carboxylesterase type B [Lipid metabolism].	1.31656e-127
NZ_CP040429.1|WP_154878926.1|32796_33435_-|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	gnl|CDD|235577	PRK05718, PRK05718, keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase; Provisional.	1.55177e-89
NZ_CP040429.1|WP_154878932.1|43849_44833_-|alpha/beta-hydrolase-fold-domain-containing-protein	gnl|CDD|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	1.26161e-22
NZ_CP040429.1|WP_025875485.1|50338_51397_+|LacI-family-transcriptional-regulator	gnl|CDD|380487	cd01545, PBP1_SalR, ligand-binding domain of DNA transcription repressor SalR, a member of the LacI-GalR family of bacterial transcription regulators. Ligand-binding domain of DNA transcription repressor SalR, a member of the LacI-GalR family of bacterial transcription regulators. The SalR binds to glucose based compound Salicin which is chemically related to aspirin. The ligand-binding of SalR is structurally homologous to the periplasmic sugar-binding domain of ABC-transporters and both domains contain the type 1 periplasmic binding protein-like fold. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the type 1 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	2.43388e-114
NZ_CP040429.1|WP_154878921.1|29142_30672_-|aldehyde-dehydrogenase-family-protein	gnl|CDD|143434	cd07116, ALDH_ACDHII-AcoD, Ralstonia eutrophus NAD+-dependent acetaldehyde dehydrogenase II-like. Included in this CD is the NAD+-dependent, acetaldehyde dehydrogenase II (AcDHII, AcoD, EC=1.2.1.3) from Ralstonia (Alcaligenes) eutrophus H16 involved in the catabolism of acetoin and ethanol, and similar proteins, such as, the dimeric dihydrolipoamide dehydrogenase of the acetoin dehydrogenase enzyme system of Klebsiella pneumonia. Also included are sequences similar to the NAD+-dependent chloroacetaldehyde dehydrogenases (AldA and AldB) of Xanthobacter autotrophicus GJ10 which are involved in the degradation of 1,2-dichloroethane. These proteins apparently require RpoN factors for expression.	0
NZ_CP040429.1|WP_059063074.1|34726_37489_+|TonB-dependent-receptor	gnl|CDD|273804	TIGR01782, TonB-dependent_receptor, TonB-dependent receptor. This model represents a family of TonB-dependent outer-membrane receptors which are found mainly in Xanthomonas and Caulobacter. These appear to represent the expansion of a paralogous family in that the 22 X. axonopodis (21 in X. campestris) and 18 C. crescentus sequences are more closely related to each other than any of the many TonB-dependent receptors found in other species. In fact, the Crescentus and Xanthomonas sequences are inseparable on a phylogenetic tree using a PAM-weighted neighbor-joining method, indicating that one of the two genuses may have acquired this set of receptors from the other. The mechanism by which this family is shared between Xanthomonas, a gamma proteobacterial plant pathogen and Caulobacter, an alpha proteobacterial aquatic organism is unclear. [Transport and binding proteins, Porins].	0
NZ_CP040429.1|WP_154878923.1|30717_32745_+|GAF-domain-containing-protein	gnl|CDD|225822	COG3284, AcoR, Transcriptional activator of acetoin/glycerol metabolism [Secondary metabolites biosynthesis, transport, and catabolism / Transcription].	2.08737e-150
NZ_CP040429.1|WP_032978442.1|51639_52488_+|5-dehydro-4-deoxy-D-glucuronate-isomerase	gnl|CDD|179169	PRK00924, PRK00924, 5-keto-4-deoxyuronate isomerase; Provisional.	1.73807e-177
NZ_CP040429.1|WP_025875493.1|45857_46862_+|TRAP-transporter-substrate-binding-protein	gnl|CDD|270389	cd13671, PBP2_TRAP_SBP_like_3, Uncharacterized substrate-binding protein of the Tripartite ATP-independent Periplasmic transporter family; the type 2 periplasmic-binding protein fold. This subfamily includes uncharacterized periplasmic substrate-binding proteins similar to TRAP transport systems such as SiaP (a sialic acid binding virulence factor) and TeaA (an ectoine binding protein). TRAP transporters are a large family of solute transporters ubiquitously found in bacteria and archaea. They are comprised of a periplasmic substrate-binding protein (SBP) and two unequally sized integral membrane components: a large transmembrane subunit involved in the translocation process and a smaller membrane of unknown function. The driving force of TRAP transporters is provided by electrochemical ion gradients (either protons or sodium ions) across the cytoplasmic membrane, rather than ATP hydrolysis. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	5.49684e-132
NZ_CP040429.1|WP_154878918.1|24841_27319_+|DNA-ligase-D	gnl|CDD|235658	PRK05972, ligD, ATP-dependent DNA ligase; Reviewed.	0
NZ_CP040429.1|WP_134831779.1|46872_47406_+|TRAP-transporter-small-permease	gnl|CDD|225632	COG3090, DctM, TRAP-type C4-dicarboxylate transport system, small permease component [Carbohydrate transport and metabolism].	2.53029e-26
NZ_CP040429.1|WP_099786335.1|33421_34441_-|sugar-kinase	gnl|CDD|238571	cd01166, KdgK, 2-keto-3-deoxygluconate kinase (KdgK) phosphorylates 2-keto-3-deoxygluconate (KDG) to form 2-keto-3-deoxy-6-phosphogluconate (KDGP). KDG is the common intermediate product, that allows organisms to channel D-glucuronate and/or D-galacturinate into the glycolysis and therefore use polymers, like pectin and xylan as carbon sources.	1.35948e-83
NZ_CP040429.1|WP_025875489.1|47409_48693_+|TRAP-transporter-large-permease	gnl|CDD|224509	COG1593, DctQ, TRAP-type C4-dicarboxylate transport system, large permease component [Carbohydrate transport and metabolism].	3.35921e-125
NZ_CP040429.1|WP_154878928.1|37625_41429_+|LamG-domain-containing-protein	gnl|CDD|379155	pfam13385, Laminin_G_3, Concanavalin A-like lectin/glucanases superfamily. This domain belongs to the Concanavalin A-like lectin/glucanases superfamily.	0.000602928
NZ_CP040429.1|WP_154878939.1|52570_53326_+|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD	gnl|CDD|188170	TIGR01832, 2-dehydro-3-deoxy-D-gluconate_5-dehydrogenase, 2-deoxy-D-gluconate 3-dehydrogenase. This model describes 2-deoxy-D-gluconate 3-dehydrogenase (also called 2-keto-3-deoxygluconate oxidoreductase), a member of the family of short-chain-alcohol dehydrogenases (pfam00106). This protein has been characterized in Erwinia chrysanthemi as an enzyme of pectin degradation. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	2.72028e-140
NZ_CP040429.1|WP_025875519.1|23911_24838_+|Ku-protein	gnl|CDD|238408	cd00789, KU_like, Ku-core domain, Ku-like subfamily; composed of prokaryotic homologs of the eukaryotic DNA binding protein Ku. The alignment includes the core domain shared by the prokaryotic YkoV-like proteins and the eukaryotic Ku70 and Ku80. The prokaryotic Ku homologs are predicted to form homodimers. It is proposed that the Ku homologs are functionally associated with ATP-dependent DNA ligase and the eukaryotic-type primase, probably as components of a double-strand break repair system.	9.53149e-116
NZ_CP040429.1|WP_154878934.1|44990_45818_+|2-keto-4-pentenoate-hydratase	gnl|CDD|226480	COG3971, COG3971, 2-keto-4-pentenoate hydratase [Secondary metabolites biosynthesis, transport, and catabolism].	4.18318e-34

Protein sequences

>NZ_CP040429.1|WP_154878928.1|37625_41429_+|LamG-domain-containing-protein
MPHRSTLSRCLLLAVALAAGPAMAAADAPTLLFHVDAGKGLEAVVAQGEAVPNFRDKVDIVDDGARGKAIQWQDDGVLAWDAPGNILAQRGTLAFDWRARYAVGEAPFVIFRVGYADHSSWDMAWLRIDWNGHGFDAFVTDANLARTRVSFRMDTPPRADQWLHLAFAWDEDQGVRLFVDGREVARVQASGDYDAALDQLGLAGRVMAPYQVQSRYNFLRGSDFQHIRVYDRMLDAAAVSALARGKAAESAVASAADDRAWRHRFGWEGAPPPPLTAASTRIRKIEFDDARDLKAWMWKATDGIAETTWPGVYNRSRLPGRNDYFQLPDWNTYVESGQHLDLTVPAGETVNRVEIRGAAFGTLAHGRDAAHATQVLATRPQGVVRSVDDIPAQTGGVLRFSNVEQETPIQEIWAYGVSEGAEPDGTVKQTYVIDSQALPDYTNLDTLRRYIEGRYPAAERSTVMALPKGAGSRRRPADSLPTQPKPIVHVLIPSGVGDAPANQPLIRSWAYSWENMHDGLDGVAIDIPALDLPATHDGLIPLNIRIKDPIWPARDMIDVSVSVQPGQKRTLWLDLRDRILTADSLWLSIASAAPGFDAKALDGAQVRLVFKPRADALKEHVADRFNQVRDNWGFLVEEHTTSKRQRLYARVYADLSDLLRVDPDHELGRLYWNYISYNSQGRPPYTAPEVPKGVPAWAFHQVQDLAQVRQFVDWWIDQRQVAYGDFGGGISDDSDLTQQWPGLALMGVQPDRLNASLTALSDAVYRNGMFSNGLSTIETDELHAYEEGINTNSAMLYLNWGDPLTLERLMETVKAFDERIILRNPQGHVLFSSNWFGGNKVYREPNWQWQKPYSFPVLHPAFLLGQYNADPTGRRLVIGLADGYLAHAGTDDKGRFTLPNEINWATGATRGGELNNGSGSGDTMHTFWAAWRWTGDAKYLQALDYRVQRGGPGALANLGENYVEALGRQQDWYPLLTAEADAGKTGFASLMAWQASGERKYIDALHAEGLQAKAQRAYMNTEGHWWSDRVEAPSEFLQRARLGGIALKRNQSWPGHTVSWRFDREGAAEQVALLVHAPSRERFTITSHNLGARVIAADMTGWNVGSGSWRVRSGVDADGDGRIDGRPRERTVQLETSVSVPMQFQPGRTEVFEFERVSAGTPVEMRPDLGVGRGDVRVDGRQVHVTVHGLGHVASGVGVAILEDGRGREIARTEVPAMAAPIDLLPKTAVVSLPLPAGERGGLRVRVALADGGEEVTRLNNVVDVPR
>NZ_CP040429.1|WP_059063074.1|34726_37489_+|TonB-dependent-receptor
MHSRNHEKKTPVTLLALAVALALAGNAGAQQQSANPNATDLDTVTVTGYRASVEKALDIKRGEAGVVDAIVAEDIGKFPDLNLAESLQRIPGVVITREAGEGRNISVRGLGPEFTRVRINGMEALTTVGAGDQSGGTNRGRGFDFNVFASDLFSQLLVRKTASADVEEGSLGATVDLRTARPFDYDGFTFAASGQASYNAMAEKADPRIAALVSNTFADGTFGALLSVAYSERQALEEGSNTGRWANGPSNGNFAASSPFAAARGADVFHPRFPRYVQMEHEQKRLGVTGSLQWKPNDATEISLDALYSKIDATRDEHYIEAISFSRGANASARLSGKPTTIVKNGEIRDNALLYGEFDNVDIRTENRHDEWSTEFKQIALNGQHRFGDDFTLSGKIGISRSKHENPVQTTVIMDKYDVDGYSYDYRGNSRAPILNYGIDPTNPNGWELAEIRLRPQYVDNDFDTGQIDFNWNISPGFRLKGGVLAKDYTFKTVELRRASELAVPNFAGGTKIVPVNLTEQAGLKGINGSPSNWVVPDLDAIAEQLDIYSNSGTFAVAPRANNVRSVEEKDRGAYLMGEFSTELGSLPLSGNFGVRYVRTKQSATGQSTLANGTVETTVSRTYDDTLPSFNLVAEVTPDFLIRLGAAKVMSRPGLGSLTPGATVAVAGGARTISSGNPMLDPIRATNVDLGFEWYFAEGAMAGIGLFYKDIESFVQTTREVRPYSDSGLPASLLVGTGASATDDFTYSKPVNTPGGELHGVEANYTQPFTFLPGKWANLGMQLNYTWVESKIQYINAAGQPVMKTDLTGLSKSSWNATLFYEGEKFAGRISATNRDDYLTQAPGQETGFNLDGYHGMTGTTVFDASIRYKISDQLELSLEGINLTNEASDEWVYSPLTGRLPLQYTETGRQYLLGLRYKF
>NZ_CP040429.1|WP_099786335.1|33421_34441_-|sugar-kinase
MGRIVCFGELLLRLGAPGRELLLQSPQLQVHVGGAEANVAVSLSRFGHDVAMVSTVAGNALGAHALAELRRHGVDTRGVREDAEGRMGLYFLTTGAVQRASEVVYDRADSAFANSTAADYDWPALLQGAQWLHLSGVSPALGADVAQATLAAARAARALGVRVSFDGNFRPKLWQRWGGDARAILHELFAQADIVFADYRDIEVILGQRFEQADVVARVEAAAAAAFEAFPQLQWMACTQRQTLSVDHHALGALLLGRDGTRAQAPVRQLQGIVDRIGGGDAFAAGILHGILSAFDADATVRFGLAAGGLKHSIPGDFNPVSEADVLALMGEERFDVRR
>NZ_CP040429.1|WP_154878926.1|32796_33435_-|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase
MSGADPRVRAVLKLAPVIPVFTPDDIDDAVQVAQALFRGGLPVIEVTLRTPRALEAIKAMVEAVPDAVIGAGTVLDAVQMQAVKQAGGRFAVSPGATPRLYAAARDADLPYLPGVATGSELIVGLEHGLDTFKFFPAVQAGGAAMLSAWHGPFGDVRFCPTGGISAQTASQFLHLPNVLCVGGSWLTTAALMQTRDWDSVERLAREAAVLAG
>NZ_CP040429.1|WP_154878923.1|30717_32745_+|GAF-domain-containing-protein
MPTVACCAASRLHRPAVGDPVARPAAAQQAWSLQGDAGCAVNRDRSRNNCRNVRHRRLSVSPLAPDPRLGSARRSFFERGAAPVGAVPEAILHSWQRCQRHGLLVDAQPAAEPLTDNRLRELRQRRERLWRQARPELDGLAAEMTHSGSIVLLTDEDGWILDAEGSAGFLDKAGRVALMPGMRWDEGTVGTNAIGTALVDGRALQVRGGEHYFAPHGILTCSAVPILDPYGQCLGVLDVSGDARLPHVHALALVRQAVAQIEHRGFADGLADCELLRLHHQPALLGSAREGVLGFRGGRLVAANRAGLALFGLDRQDIGRTPYEALFEQPLSRLADDGVLLDRQGRRLYGVREARASRRSVATPGPTAPLPASAQGPLFDTGQQQQLATAGRVLQAGLPVLLQGETGTGKEVFARELHARSTRAGKPFVAVNCAALPEGLIEAELFGYEEGAFTGARRQGSPGLLRQAEGGTLFLDEIGDMPLALQPRLLRVLQERELSPLGGGKPVKLDFALVCASHCELPQAVDAGRFRADLYYRIADHVVTLAPLRQHPDRAAVVDALWQQLGQGHALSSQARAALAAHAWPGNLRQLSACLRTLAALAEPGQPVGPQLLPADVRAGTPTAPAVPASGALEEIAEAAMRQALAECQGNVSAAAKRLGINRSTLYRRLGTPRG
>NZ_CP040429.1|WP_154878921.1|29142_30672_-|aldehyde-dehydrogenase-family-protein
MNAVPSTRPHATDPRSLFKPRYGNYIGGEWIAPRSGQYFDNISPVNGQVFTEVARSNAEDIDAALDAAHAAKDAWGRTSAAHRALLLNRIADRIEQNLELLAHAETWDNGKPIRETLNADVPLMADHFRYFAGCLRAQEGSLSQIDDDTVAYHFHEPLGVVGQIIPWNFPLLMAAWKLAPALAAGNCVVLKPAEQTPASILVLMEVIGDLLPPGVLNVVNGFGLEAGKPLASSPRIAKIAFTGETSTGRQIMQYASQNLIPVTLELGGKSPNLFFADVMAEDDDFLDKAVEGFVMFAFNQGEVCTCPSRALVQESIYERFMERALERVAAIRQGNPLDPNTMVGAQASGEQLEKILSYIAIGREEGAEVLIGGDKAALGGDLAGGFYVQPTVFKGHNGMRVFQEEIFGPVVSVTTFRTEEEALQIANDTLYGLGAGVWSRDAARLYRVGRAIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHRMMLDHYQQTKNLLVSYAPKKLGFF
>NZ_CP040429.1|WP_025875513.1|28039_29068_-|alcohol-dehydrogenase-AdhP
MNRTMKAAVVREFGKPLVIEEVVVPRPGAGEVLVKIEACGVCHTDLHAAEGDWPVKPNPPFIPGHEGVGHVVAVGGGVGHIKEGDRVGIPWLYSACGHCEHCLGGWETLCETQRNTGYSVNGGFAEYALADANYVGLLPKEVGFVEIAPVLCAGVTVYKGLKVTDTKPGDWVAISGIGGLGHMAVQYARAMGLNVAAVDVDDAKLALARRLGAQVTVNARTTDPAAFLKKEIGGAHGALVTAVSPKAFEQALGMVRRGGTVSLNGLPPGNFPLDIFGMVLNGVTVRGSIVGTRLDLQESLQFAAEGKVAATVSTDRLENVNEVFARMHAGTIEGRVVIDFAA
>NZ_CP040429.1|WP_025875515.1|27544_27934_-|hypothetical-protein
MPGTLKTVFLSLLALIGALLALALVSSAAGWLPSLLRMTPGSEAQLGWDLAFTVLGGIAAIAFATYYAPCWPRAHGTSIWSLLVLGAGYGLWVMGGDFPHWFVIGLLVSLPVQLLLGWWFGRRASRDRR
>NZ_CP040429.1|WP_154878918.1|24841_27319_+|DNA-ligase-D
MSLHQYRRKRRLGGGSGQTPEPDDAPARGNPKRRPIFVVQLHHASSRHYDFRLEMDGVLKSWAVPKGPSLRVGEKRLAVEVEDHPLSYAGFEGDIPQGHYGAGHVDVFDHGSWACEGDPLQALAAGKIDFLLHGQRLAGGWKLVRTAMKGRQVQWLLIKRDDAQARDAEADDLLHTPARTSAKRSRVSAKKTAPAPRAAHPRKADARWHARALQLDEARDKSYPHQFKPQLTDHRDTAPDGERWLHEIKWDGYRLLADVHEGEVTLRSRNGLDWTADFPEVVQALQALPVRDARLDGELVVLDDNGRSDFAALQRVIDGSSKQPLRYIVFDLPGVAGVDISRAPLLQRKALLKELIGDAVGTLAFSEHVIDHGPAVFEASGKAGFEGIVSKQVDAPYVNTRARSWVKVKHEDTDEFLIIGHTAPKGSRVGFGSLLLATPDKGGLRYVGRVGTGFDDEGLRALAATLAPLAVKEAVLPLPAHVPFRAASVRWVKPVTVAEVAFRGWGKEGLLRQASFKRLRSDKKKEDLAMSATPADDGDDVAITHPERVVFAKKKLSKGDVADYYRQMARWILPEISGRPLSLLRCPDGVGKACFFQKHHGQGLGDAVHAVPLQQKSGREDYVYIDDERGLLQLVQMNTLELHPWGATVADPEHPDRLVFDLDPGEGVSWADVKRGARDVRDRLQQTGLQSFVRLSGGKGVHVVVPLQPAADWDEAKAFCEAFAQAMAEQAPDRYVATMSKAKRSGVIFIDWLRNTRGATSVCSWSLRARESAGVAVPLRWEELARVSAADAFPMDKALARAKRLKADPWQGIDALKQTLPTLQR
>NZ_CP040429.1|WP_025875519.1|23911_24838_+|Ku-protein
MARPIWTGTLSFGLLNVPVSLMSGERKVDLHFRMLDSRDRKPIRFERVNADTGEEVPWKDIVKAYEYDKGSYVVLEEDDIRSAAPESHETVEVETFVDASQIDPRYYEKPYLLVPGKKAEKGYVLLRETLRSTGKVGIARVVVRTREYLCAVMPNDDALVLMILRYPQELVEPDDYKLPSGKLADYRITSKETAMAEQLIESMAGDWDPSQYHDEFRERLQQVLNKRIKSKGGTTQVEDEPAPREDATTNVVDFMALLQKSLDANKRTPAKKAAARKAPAKKAAAKKAPAKKAAKKAAKKTPARRKAG
>NZ_CP040429.1|WP_154878930.1|42230_43853_-|carboxylesterase-family-protein
MNQGDANLQRRRFLRDSARWALATATLAALPAAAVPGPRDDTQVVARLRAGRVRGQREHGVHVFRGLRYGADTSAYRFQPPRRETGWRGIADALEYAASAPQSGADGPGSEDCLFLNVWTPALGDGGKRPILVYIHGGGFNNGSGSDPLYDGSALCRRGDVVVVTVNHRLNTFGYLYLGALGDPRYAASGNVGQLDLVQALQWVREHAAVFGGDAGNITVFGQSGGGAKIATLMAMPAAKGLFQRAWTMSGQQVTAAGPRAAAQRTSIAMETVAARDLQALLRLPATELLAATRARDPSRVESSALYFGPVLDEVVLPVHPFWPQAPAQSASIPMVIGNTRDETRAFLGNDPANFTLTWEDLPAQLEKQQFVDLLPSVVIAEYRRLYPHYTPSEVFFAATTAGRSWRGAVEELEARARQTTGAAPTWAYQLDWPSPVEDGRLRAFHTLDIPLVFDNAGLPGARTGGGEDARALAATMSDALIAFARTGDPNHAGMSQWAPYGVPQRQTMVFDRHSRVVDDPRAGERALYARVPFVQRGTQ
>NZ_CP040429.1|WP_154878932.1|43849_44833_-|alpha/beta-hydrolase-fold-domain-containing-protein
MRFSRVLLLLSGLLLTIPASAAAVPLRAGEHLGQELAGEQLPLWPAGQVPGETGTSRPARVVERSDDPAHPDRFIDQVDAPYLLVHTPARANGRALLVIPGGGYQRVVIDKEDSALVPEWVDRAGYTLFVLRYRLPQAGRDRQAALADAQRALRVVRDQAARRRLDADSVSVMGFSAGGHVAARLATGFDAPVYPPRDAIDRLSARPARAVLVYPVIDMGAHAHSGSRGRLLGEQPDAALAAQYSMQQHVRADMPPTLLIHANDDRVVNVHNSEVMAQALAKAGVEHELHLFAHGGHGFGMRMPPDSTLAVWPLLAQRWLQATEAAH
>NZ_CP040429.1|WP_154878934.1|44990_45818_+|2-keto-4-pentenoate-hydratase
MSNEHGIHGQTPAPDDAAAIAHAFTTARRSGQALPGFPGLVPPDLVAAYQVQDLAIASWDDQVVGWKVGYIAAERRDASGDDRLLGPVFSRQLKNATGGTVDIPVFVDGFGAVEAEYVLELLEDAPAAQLHWTPEQAEALPARLYIGVEVASSPLATINELGPRVVVSDFGNNNGLVLGPEIADWTARDETDLRAETLIEGEVVGTGGATRLPGGLRAAYAFALSRSALRGRPLRRGDLIATGNATGIHDITVGQTALVRFAGFGEIACRAVPAG
>NZ_CP040429.1|WP_025875493.1|45857_46862_+|TRAP-transporter-substrate-binding-protein
MITRRHFLAGGAAALATPMLAACGRGPADAIDGGQLLTATDVHVADYPTVTAVKWIGETLQRESNGRLRLRQYHSGQLGRESEAIDMARFGAIDITRVYAGALNNAFPLTQALCLPYVFESVAHQRAALDGGIADAVLRGFESRDLVGLAIYDSGARCFYNTKHPIVQPGDLHGLKLRVASSDIFIQLMRLLGANPTPMSLGDTFSGMETHMIDGAENNMRSFHSSRHFEAAHYWSQSDHSYAPDVLLMSRASFERLQPADRQLLLETARASVKVMREQWDASEDAARRAVLASGVKANEVDLPAFRAAAQPLLQQYLQQPELAALVARIRAAA
>NZ_CP040429.1|WP_134831779.1|46872_47406_+|TRAP-transporter-small-permease
MTETTISTGPGPGQRLLDRIADIAIHVAVAALLGLVVVQGWQVFARYVINDSPSWTEPVTLLLLATAMSLGAACGVHTNRHFGFFLLHAYMGPGLRRVVDVFTQLVVAVLGGFIAFWSADLLLDGMDIKTAGANLPQSINYLPLAVGGALMLLFALNRAWKALHATAADADDAEGDR
>NZ_CP040429.1|WP_025875489.1|47409_48693_+|TRAP-transporter-large-permease
MGITILFSVFAALLLLGVPVAYALAAAALATLLYLDIPSIVLVQQISAGTGSASLIAIPLFIFAGEIMMRGGISERLIALASSLVGRMRGGLGQVSILSSLFFGGVSGSAIADVSAVGGTMIPQMVKRGYDRDFAVNVSITAALVALLVPPSHNLILFSAAAGGGLSIADLFAAGIVPALLMTLALMITGYVVARRRGYGVEVFPGWRAVLLRIVSALPGLGLVALIFVGIRAGIFTAVESAAIAVVYALLVTTVLYRQLRWREFFDTVIHAARSTGVILFVIATAAVFGWLLAYLQVPAAAVDFLQSFAHSQFMVLLMIVVMLLLLGTFMDLAPMILICTPIFLPVAKAYGIDPIHFGLVLVLTGGLGLVTPPVGSVLFIGTAIGKISVGQSMRTIWPFWFAALGVLLIVTFFPSLSLWLPAALRA
>NZ_CP040429.1|WP_154878936.1|48710_50300_+|family-43-glycosylhydrolase
MTPTLHRTAATALLGLLLAALPALAADPAPAQWKRGIEHQRQGDLGNGTFLNPVLAGDRPDPSVLKDGEDYYLTLSSFDAYPGLPIWHSRDLVNWQPLGHAITQNVGAIWAPDIVKHHGRYFIYFPARTGERRSNFVVWADDIKGPWSAPIDIGLGGYIDPGHAVGEDGKRYLFLSGGDYVQLADDGLSVVGTPKHVYDGWRYPESWDVEAYAQEGPKIHFRDGWYYMTTAVGGTAGPPTGHMVITARSRSIHGPWVNAPNNPIMRTRSAAEPWWSRGHATVIEGTDGRWWMMYHGYENGFWTLGRQALLEPIEWTADGWFVAKGGDLGQPLRKPSGSALAPHGMALSDAFTGRTLGPQWAFFNPALDEYRRLRFSGDGLVLQGKGSTPRDASPLTTIAGDPAYQFEVQMEIAPGAVGGALLFYSDRLYVGVGSNGEQLVMHRYGEERPTRLAASAKGGRLWLRVTNNRHIVTIHSSADGQTWQKYPVQMEVSGYHHNVAGKFLALKPALYAAGNGAVTFRSFRYRALD
>NZ_CP040429.1|WP_025875485.1|50338_51397_+|LacI-family-transcriptional-regulator
MSVRNKNDAATPALAKGKAATINDIARLSGVSKKTVSRIINNSPLVRKDTRDKVEALMREVGYTPDPLARGLAFRRSFLIGMVYDNPTAQYIVDMQYGALDALRGSSFELVVHPCDSRSPGYIDGVRRFAQQQKLHGVILVPRASEDQALADMLDEIGCRFTRVAALPLDETSQMVVTHDRDGAAEAADYLLSLGHRDIALVTGPSAYRSAHERTAGFIEALSQRGIELPKDRIIEAGYTFESGVAAAEKLLLGKRRPTAIFTGNDEMAAGIYKVALRAGINIPRQLSIVGYDDSPLASRLWPSLTSVRRHTRDTGRTAAAMLIQPEGQPALQIASVRPHLIVRDSCQPPED
>NZ_CP040429.1|WP_032978442.1|51639_52488_+|5-dehydro-4-deoxy-D-glucuronate-isomerase
MYCKTHYATHPDAIKGASNDQLRELYLLDGLFNADAVTLKYTHYERFVLGGAAPVNGPLSLPAQTEPASAAGHPFLERRELGIINVGSGTGTVTVDGTVYTLGPKDGLYVAMGSKDVVFASQDAANPAQFYLASTPAHARFETKQLSIKDAVALDRGALETSNERTIYQYIVPATCQSSQLLLGLTVLKPGSVWNTMPPHLHDRRSEVYFYFDLGDSDRVYHFMGEPDAQRHIVIQNNEAVVSPPWSIHMGAGTSNYAFIWAMGGENLDYTDMHVLDICQLK
>NZ_CP040429.1|WP_154878939.1|52570_53326_+|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD
MTNPFSLEGKVALVTGGNTGLGQGIAVALAAAGADVAVAGIAPATETIEKITALGRRCLAVEANLISIEPVERVVRETLEGLGGLDILVNNAGLIRRADAVDFSEQDWDDVMNVNIKSAFFISQAAGRHFIAQGSGKIINIASMLSFQGGIRVPSYTASKSGIAGITRLLANEWAGKGVNINAIAPGYMATDNTAALRADQDRNKAILERIPAGRWGTPEDLAGAAVFLASSASDYINGAVLPVDGGWLAR

Crispr_ID: NZ_CP040429_2

• CRISPR_ID: NZ_CP040429_2
• CRISPR_location: 113894-113997
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: cas3

Consensus repeat of NZ_CP040429_2

Consensus_repeat	Method
AGTAGATCCACGCCATCCGTGGATG	CRISPRCasFinder

spacers of NZ_CP040429_2

>2.1|113919|54|NZ_CP040429|CRISPRCasFinder
AAACGCGCGGACGGCCCGGCGCCAACCAAGGCGGCATCTACCCTGCACGGCATC

CRISPR arrays and Neighbor proteins around NZ_CP040429_2

CRISPR arrays

The CRISPR arrays of NZ_CP040429_2

>merge|NZ_CP040429|2|113894-113997|CRISPRCasFinder
AGTAGATCCACGCCATCCGTGGATGAAACGCGCGGACGGCCCGGCGCCAACCAAGGCGGCATCTACCCTGCACGGCATCAGTAGATCCACGCCATGCGTGGATG

>NZ_CP040429|2|2|113894-113997|CRISPRCasFinder
AGTAGATCCACGCCATCCGTGGATG	AAACGCGCGGACGGCCCGGCGCCAACCAAGGCGGCATCTACCCTGCACGGCATC
AGTAGATCCACGCCATGCGTGGATG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_154878982.1|115875_118041_-|hypothetical-protein	unknown	unknown	gnl|CDD|372724
NZ_CP040429.1|WP_080150268.1|127189_127804_+|DUF938-domain-containing-protein	unknown	unknown	gnl|CDD|253548
NZ_CP040429.1|WP_140228156.1|119155_120052_-|DUF58-domain-containing-protein	unknown	unknown	gnl|CDD|224635
NZ_CP040429.1|WP_105163209.1|103148_103493_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025876012.1|121763_123098_-|TldD/PmbA-family-protein	unknown	unknown	gnl|CDD|223389
NZ_CP040429.1|WP_154878984.1|118037_119159_-|hypothetical-protein	unknown	unknown	gnl|CDD|131281
NZ_CP040429.1|WP_154878986.1|120059_121043_-|AAA-domain-containing-protein	unknown	unknown	gnl|CDD|223786
NZ_CP040429.1|WP_154878968.1|102099_103161_+|DNA-topoisomerase-IB	unknown	unknown	gnl|CDD|226099
NZ_CP040429.1|WP_154878988.1|121056_121764_-|DUF4159-domain-containing-protein	unknown	unknown	gnl|CDD|379342
NZ_CP040429.1|WP_154878971.1|104825_105905_-|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_CP040429.1|WP_154878973.1|106524_108468_+|transmembrane-BlaR-protein	unknown	unknown	gnl|CDD|310280
NZ_CP040429.1|WP_025876036.1|106134_106521_+|BlaI/MecI/CopY-family-transcriptional-regulator	unknown	unknown	gnl|CDD|367747
NZ_CP040429.1|WP_105163214.1|112664_113195_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154878990.1|123119_124754_-|TldD/PmbA-family-protein	unknown	unknown	gnl|CDD|223389
NZ_CP040429.1|WP_154881297.1|124781_126365_-|TldD/PmbA-family-protein	unknown	unknown	gnl|CDD|223389
NZ_CP040429.1|WP_154878975.1|108553_108877_-|hypothetical-protein	unknown	unknown	gnl|CDD|288556
NZ_CP040429.1|WP_154878977.1|108966_109986_-|exonuclease	unknown	unknown	gnl|CDD|379215
NZ_CP040429.1|WP_025876028.1|109982_112472_-|DEAD/DEAH-box-helicase	cas3	cd09710_cas3_CAS-I-D	gnl|CDD|224126
NZ_CP040429.1|WP_154878969.1|103710_104829_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235853
NZ_CP040429.1|WP_154878980.1|114073_115879_-|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP040429.1|WP_025876028.1|109982_112472_-|DEAD/DEAH-box-helicase	cas3	cd09710_cas3_CAS-I-D	2.7e-14	47.6	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_080150268.1|127189_127804_+|DUF938-domain-containing-protein	gnl|CDD|253548	pfam06080, DUF938, Protein of unknown function (DUF938). This family consists of several hypothetical proteins from both prokaryotes and eukaryotes. The function of this family is unknown.	9.28924e-78
NZ_CP040429.1|WP_140228156.1|119155_120052_-|DUF58-domain-containing-protein	gnl|CDD|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	1.13673e-32
NZ_CP040429.1|WP_154878982.1|115875_118041_-|hypothetical-protein	gnl|CDD|372724	pfam13779, DUF4175, Domain of unknown function (DUF4175).	1.55504e-06
NZ_CP040429.1|WP_025876012.1|121763_123098_-|TldD/PmbA-family-protein	gnl|CDD|223389	COG0312, TldD, Predicted Zn-dependent proteases and their inactivated homologs [General function prediction only].	2.44333e-70
NZ_CP040429.1|WP_154878984.1|118037_119159_-|hypothetical-protein	gnl|CDD|131281	TIGR02226, hypothetical_protein-transmembrane_prediction, N-terminal double-transmembrane domain. This model represents a prokaryotic N-terminal region of about 80 amino acids. The predicted membrane topology by TMHMM puts the N-terminus outside and spans the membrane twice, with a cytosolic region of about 25 amino acids between the two transmembrane regions. Member proteins tend to be between 600 and 1000 amino acids in length. [Hypothetical proteins, Domain].	8.34331e-15
NZ_CP040429.1|WP_154878986.1|120059_121043_-|AAA-domain-containing-protein	gnl|CDD|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.85561e-95
NZ_CP040429.1|WP_154878971.1|104825_105905_-|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.	1.631e-61
NZ_CP040429.1|WP_154878988.1|121056_121764_-|DUF4159-domain-containing-protein	gnl|CDD|379342	pfam13709, DUF4159, Domain of unknown function (DUF4159). Members of this family are hypothetical proteins.	5.11302e-67
NZ_CP040429.1|WP_154878968.1|102099_103161_+|DNA-topoisomerase-IB	gnl|CDD|226099	COG3569, COG3569, Topoisomerase IB [DNA replication, recombination, and repair].	2.93668e-98
NZ_CP040429.1|WP_154878973.1|106524_108468_+|transmembrane-BlaR-protein	gnl|CDD|310280	pfam05569, Peptidase_M56, BlaR1 peptidase M56. Production of beta-Lactamase and penicillin-binding protein 2a (which mediate staphylococcal resistance to beta-lactam antibiotics) is regulated by a signal-transducing integral membrane protein and a transcriptional repressor. The signal transducer is a fusion protein with penicillin-binding and zinc metalloprotease domains. The signal for protein expression is transmitted by site-specific proteolytic cleavage of both the transducer, which auto-activates, and the repressor, which is inactivated, unblocking gene transcription. homologs to this peptidase domain, which corresponds to Merops family M56, are also found in a number of other bacterial genome sequences.	3.07405e-47
NZ_CP040429.1|WP_025876036.1|106134_106521_+|BlaI/MecI/CopY-family-transcriptional-regulator	gnl|CDD|367747	pfam03965, Penicillinase_R, Penicillinase repressor. The penicillinase repressor negatively regulates expression of the penicillinase gene. The N-terminal region of this protein is involved in operator recognition, while the C-terminal is responsible for dimerization of the protein.	1.73347e-30
NZ_CP040429.1|WP_154878990.1|123119_124754_-|TldD/PmbA-family-protein	gnl|CDD|223389	COG0312, TldD, Predicted Zn-dependent proteases and their inactivated homologs [General function prediction only].	6.08134e-101
NZ_CP040429.1|WP_154881297.1|124781_126365_-|TldD/PmbA-family-protein	gnl|CDD|223389	COG0312, TldD, Predicted Zn-dependent proteases and their inactivated homologs [General function prediction only].	1.1332e-97
NZ_CP040429.1|WP_154878975.1|108553_108877_-|hypothetical-protein	gnl|CDD|288556	pfam11720, Inhibitor_I78, Peptidase inhibitor I78 family. This family includes Aspergillus elastase inhibitor and belongs to MEROPS peptidase inhibitor family I78.	2.20358e-07
NZ_CP040429.1|WP_154878977.1|108966_109986_-|exonuclease	gnl|CDD|379215	pfam13482, RNase_H_2, RNase_H superfamily.	2.34918e-48
NZ_CP040429.1|WP_025876028.1|109982_112472_-|DEAD/DEAH-box-helicase	gnl|CDD|224126	COG1205, COG1205, Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster [General function prediction only].	0
NZ_CP040429.1|WP_154878969.1|103710_104829_+|SDR-family-oxidoreductase	gnl|CDD|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	1.74707e-164

Protein sequences

>NZ_CP040429.1|WP_105163214.1|112664_113195_+|hypothetical-protein
MAVAKRATQVALLAGMLLAGIAHAQQTTPAAVPVPTPDPVPAPAVPPAADDAPVVLPPAQGNVTTLGEVRALKPEDDQPLDLYRFKNPMRAENNRFSRDWSEPPSPEQVSMGGGYIMMGVVKGVMAAAKGLNKITGGPDQIQSAIARPPPELSAEQQRRALQFCAQQDGCGAPPEK
>NZ_CP040429.1|WP_025876028.1|109982_112472_-|DEAD/DEAH-box-helicase
MAYELAKRTADAEQQLATRDGLPARDGALLSARLQRRYQDRITGSFAIPGREGRYAPIPDSVPPALTAALKARGIEQLYSHQAEAWEASQRGDHVAIVTPTASGKSLCYTLPVVSAAMQDKAKALYLFPTKALAQDQVAELLELNRAGDLGVKAFTFDGDTPGDARQAIRLHGDIVVSNPDMLHQAILPHHTKWAQFFENLRYIVIDEVHTYRGVFGSHVTNVLRRLKRICAFYGVQPQFILCSATIGNPQAHAEALIEAPVTAITESGAPSGPKQVLLWNPPVINPDLGLRASARSQSNRIARIAIKSGLKTLVFAQTRLMVEVLTKYLKDIFDHDPRKPPRIRAYRGGYLPTERRETERAMRAGNIDGIVSTSALELGVDIGSLDVVILNGYPGSVAATWQRFGRAGRRQQPALGVMVASSQPLDQYVVRHPDFFAEASPEHARIAPDQPLILFDHIRCAAFELPFRVGDGFGPIDPEVFLEALAETEVIHREGERWEWIADSYPANAVSLRAVADGNFVVVDRSDGRQQIIAEVDYSAAALTLYEGAIHMVQSTPYQVETLDWEGRKAYVTRTHVDYYTDSIDFTKLKVLDRFDGGVAGRGDSHHGEVHVVRRVAGYKKIRYYTHENIGYGPVNLPDQELHTTAVWWQLPQALLLRAFASKQDALDGFLGAAYALHIVATVAVMADARDLQKSVGNGDGTWIAIADQSGRGQLRGSDGEPGAVELLQEFVPTVYLYDNFPGGVGLSEPLWQRQAELVQRARELVQRCDCKAGCPACVGPVLAAQEQDETSPRALALRVLDLFDAQACQQVADVVVSTRDPMELIAP
>NZ_CP040429.1|WP_154878977.1|108966_109986_-|exonuclease
MSLSLDKLRLLRKQAGDPKAATPAAPTQQTPPALMAANDARQPPAERSVFAWVEQEIRHKPTGTATATPAPAALRRPEVGSLHRLLGMRSRGGPAPARASAQDRQLPGNEIAPGLFLIESLLPQPIPAMPLSLAFAKREGEHVAARDLLFFDTETTGLAGGTGTRAFMIGAADWHVCRQRGEGLRIRQLLMSTMAAEEEMLAAFASWLQPHTVFCSYNGRSYDAPLLKTRYRLARQADPITALDHVDLLYPTRRRYRGTWENCKLSTIERQLLRVVREDDLPGSEAPAAWLRYLRGGDALNLRRVADHNHQDVVTLALLLQRLVREEQRERETLALVSG
>NZ_CP040429.1|WP_154878975.1|108553_108877_-|hypothetical-protein
MRRSPLLLLAAILPLAACSHAGGNASADAGSLPAKVSDGPQECRPEALDAFTGKTADEATMKKLVADSGARNARVVKPGMAVTMDFRQDRVTVQVDAQNRIERASCG
>NZ_CP040429.1|WP_154878973.1|106524_108468_+|transmembrane-BlaR-protein
MDTSMLIPMLERLGWTSLQTVLLVALVYVLCRALPALSAATRCRLWWLVSLQAVVGLLWSQPLQLAWLPAPDAVAMTTVDLAADAIYTMAPEASAHLLANTPMADVGSTPVAWWALALAALWMSGVLLMALRTFGEWRRCRALLAASYPCEDQALVQALQLASDAHGLRRAPRLWMSDQVDAPQLVGPFRPVLLLPAGMNALQGDALDLALTHELQHLQRRDLQWGLLPALAQHLFFFHPLLRLAVREYAQAREEAVDAAVVGQHGASRHAYGRLLLQLGVAPQPHLGVASAAPSTTSLKRRLLSLQSHRACPRLLAVGLTLVVLAVGVAPMRLVAAPVPPAPPAPPRAVPAPPPPPAAPPAPAAPPAAAVPAEPADWAEPAEPAEPEEPADVNEDEEQDAGTHAHSQTTIVTHGQLDLGTPPQQAFVLVDHGQAFANAGMDDVMQARSRLGDGPALWFRQGDKRYVVRDPMLIQSLQRAYAGAVDLSRQQSELGRQQSVLGRQQGQLGREQGELGRLQGEEAREIALAAARAARSAINDRDINREAAAEAARATRGAVDDAAIARKAAAEAQRASQVARNQALQSERSREMSRLASQQAALGSQQAALGSQQAALGERQARLQAQAAKQAEQVIARALASGKAERL
>NZ_CP040429.1|WP_025876036.1|106134_106521_+|BlaI/MecI/CopY-family-transcriptional-regulator
MRGKTIGDQELALLQYVDEQAPASVGEVASGYGEPRGLARSTVLTMMERLRAKGYLQRRQQQGVYRYQPTRGPESVLQGAVAQFVDNTLQGSVSPFVAYLSQRQKVSDNELAELEALVAELQSRRQED
>NZ_CP040429.1|WP_154878971.1|104825_105905_-|serine-hydrolase
MIISLLPFAAVSANQDQANDQTRRFIRQTMQEQRIPGLQIAVVKDGQVVLSETYGLANVENGVVATRSTRFPLNSATKSFTGVALARLAQDGRVDLDAPIARYLDDLPESWRAVRVRQLLAHTSGLPDILDAEGLLGGGSEQDAWQAVRALPAEARAGERFQYNQTNYLLLARIIARQSGMPYERFLATGQFSTARMARTTFGDSYDLIPDAATMYSYLPRATDAKDATPRLSHWFYDMPPSLWAGGGILTTADDTARWLVALQEGRLLELRAVQQMWSAEHLNDGSAGDWAAGWPVFNTAPDLQVGGMGGARSAFIVYPERELAVVVLTNLVGANPQQFIPRIAGFYTAAPKGVAAAR
>NZ_CP040429.1|WP_154878969.1|103710_104829_+|SDR-family-oxidoreductase
MATTKKTPARRKASPKVRKGTQAAPAAAEATTSDRPRVVKTATRKAAASDPRAARVAARQRRLQDQEKAKDVRVAKKAAKKKTATQAGPRHQPEKMPAQHLAKPGHEHALELAPRFLAPDYVGSGKLQGMRAIVTGGDSGIGRAVAVLFAREGADVAVLHLDEAKDAELTRQHVEKEGGRCVVIAGDVRDPRFCNKAVKQVAKAFGGIDILVNNAAFQLHCERLEDLEDAHLQETLQTNIGGYIQMARAVLPHLGEGASIINTGSETGLFGSKALIDYSATKGAIHAFTKALASQLLPRGIRVNCVAPGPVWTPLNPADKQAKDVAEFGKDSDMGRPAQPEELSPAYVFLASPACASYISGVILPVMGGPRG
>NZ_CP040429.1|WP_105163209.1|103148_103493_-|hypothetical-protein
MKHAIATAAVCFALAACSSSPVTQVQPIDGVISGQCHTDKVRGAVGLAASGMTIERARVDSDSLHVQVTRGSRERSGNTASGAADPAAGAATEGGDRLTIETGRTNNITAIYCG
>NZ_CP040429.1|WP_154878968.1|102099_103161_+|DNA-topoisomerase-IB
MPATPTPERQAARAAGLRYVDDTQPGFSRIRAGKGFSYRDADGHAVRDAATLQRIRALAIPPAYTAVWICARADGHLQATGRDARGRKQYRYHADWAAVRDAGKFDRTIAFGQALPALRRRLGRDLKRSGFPREKVLAVVVALLADTLVRVGNETYAQENKSYGLTTLRNRHLDLLRGGRVRMRFRGKSGQLQEVVVGDRRLGALVRSVQQLPGQALFQYRDDAGEVQPVDSGAVNDYLREVMGEDFTAKDFRTWGGTMAAVQAFAATELPEPASQRALAKAQREVVCQVAARLGNTPAVCRKAYIDPCVFAGWERGELTALAGLRGPRQWEQATLKVLRRARRLSRKAGQPQ
>NZ_CP040429.1|WP_154878980.1|114073_115879_-|hypothetical-protein
MSTSPLNVWVAVALALIVLVASARQLRSPTRGRGRLIAVLTLQAAAAALLYVCLLPPSQRASLAGLVVIGAGADKTGALPTGGTRVLLPEATDMAGAARVPDLATALRRYPSSTVTLIGAGLAARDRDAALPADTRWQAPPAANGWIALQPPADAAPGARFDVHAQARGVDRAQAELLDPAGAVVDRAPLAADGHVQLSGIARAEGRSVFQLRLLDAQGHVADSVPVPQQTLAAAPLRVLVRSAAPGAELKYLRRWATDAGIRVQVQAETGAGLSLGDGNVALDASTLARSDLLLLDERSLAALGAAQLAAVRQALRDGLGLLVRSTGAPSASARQRLRDLGLPVQGDAGSQVAAMPGEGDATMLQARRGPLAAGTLPTADGEDADRASHAAALPVLEYLALQAADSRPLLQDRDGKPIGGWRAVGKGRIGLLPITDSWRWVLAGREDRHGELWSTVFAALARAQPGTEGPWSTQALAWAGERQSLCGVQAPLRAFDGRGDGVPLIVDSTTGTARCAGWWPRQAGWQRLQHGDRTQWRYVFDPKQAPALHRQAMTDATAQRLATAAPATTQASQRVPGTRWPWWLAFVLCASLLWWLERRR
>NZ_CP040429.1|WP_154878982.1|115875_118041_-|hypothetical-protein
MKALQQAWQRARRRRAAITLLLGLPWALASAALALRVSGFDIACVVATVALLIIAAAATMRARQLDRRWLQRRLDASGASGDSADLLFADGAALNPLQQRQRTHVLAALEHNLPELRPRWPRRAVALCWIGGIVVAVLALGWPHSGAPRPTAPASPQSSAKAGPLRLQSTRLRIDAPAYTGQPTRTQNALDAKVAADSRLSWSLRFDRAPSNAWLQFHDGRRLPLRERNGEWQAQDVARTPVLYRVVSEPALAGTRLHRLDVVADRAPTVRVIDPATSLVLGTPGQRQWTLRFEASDDHGVSAQATLSITITQGSGENITFVRRSVTLSGSGEPKARRFAHTLDLAALGAQPGNDVIAQLEVRDNHAPAAQIGRSSSVILRLPSAEAVLGAELEGRIKKTLPAYFRSQRQIIIDAEALIRERRSVAADTFVKRSDAIGVDQRILRLRYGQFLGEESEGAPKPPPTSDLPTSDTPAADAHDDDHEHGHGAEAGAHDEHGHDHGGAASGNDTPPVFGSATDVLSEYGHTHDHAEAATLLDPQTRATLKAALDQMWSAEGELRQGRPEQALPFAYKALAFIKQVQQAERIYLARVGPELPPIDESRRLSGDRAGLASRDLPLAARTPPDPAVVEAWQRLGDEDGTPDLDMLATWQQRNNAFLPDALDLAAAIEQLRIDPGCTECRQRLRAQLWRALQRPLPQVMRRRAADAMGQRYLDALEAQP
>NZ_CP040429.1|WP_154878984.1|118037_119159_-|hypothetical-protein
MSLLFPLGLAALAAWLLPLLIHLARRHPYTPLDFAALRWLRAQVRPRQRIRFDDWPLLLVRLLLLAALALLLARPALTGPAPVPAAWTVVAPGLDATALRGSTDARNWHWLAPGFPTVDQPAPANAAALPSLLRELDAQLPAGTALTVHVPDPLPGLDGARLQLSREVQWQPHALAVTAPPHASPAPRLRTRSDAPAAALQWLGALQRAWSTQPLAAPLADDALPARGEIGVWTATDALPGTWQRWLQQGGTVLTAAKPPAGAPVLLRDADNAPLLWQQRIGQGRLLHLPGEWNVARNSALRDDGLPRDLLQALQPPSTPQLGDARDQAPRQAPLPAATPPLREPTAWLLLVIVLLFTLERWMASSARRRAAP
>NZ_CP040429.1|WP_140228156.1|119155_120052_-|DUF58-domain-containing-protein
MTAGTPLLLPPDLRARLRALRLRPRLASGASGIGQHASRSRGAGLEFAQYRAYEPGDELRQIDWKLYARSDRFFVRESERESPIAVWLLLDATASAGQSDRTAPGRSRLDHMRQLAACVVELALQQGDRFGLLAINGEGLQLVPAAQGARQRDRVHLQLHALQARGAWPAAERLRPLWERVRPGDLLLAIGDGFDDAGIVLLEQLASARREVMLLQVLTADERDFPFDAGHRFRDPETGDELLGDGAAIRADYLQRFAQARAALQSRLQASGIACATGWLDQPLDQPLQALFGRRGGA
>NZ_CP040429.1|WP_154878986.1|120059_121043_-|AAA-domain-containing-protein
MTSPDLDSLLPRLHALRSALAHAVVGQHTVVEQLLIGLLAGGHCLLEGAPGLGKTLLVRSLGQALELQFRRVQFTPDLMPSDILGTELLEEDHGTGHRHFRFQQGPVFTNLLLADELNRTPPKTQAALLEAMQERTVSYAGTTYTLPAPFFVLATQNPIEQAGTYPLPEAQLDRFLLHVLVDYPSEEEERQILEQTTGGATESVPKVMDAEAVIALQAAVRQVHVSPDVLAWITRLVRASRPGDGAPAAINQWVKWGAGPRAGQSLVLAAKARALLQGRFAATREDVQALAAPVMRHRLLLSFAAEAEQKRADDVVAALLQAVPFPG
>NZ_CP040429.1|WP_154878988.1|121056_121764_-|DUF4159-domain-containing-protein
MDRRACLRWLAAAASAAALPAWAQAGPRSSRYDFWFTRLQYDSGDWDVDARMPSNLITSLIDYTSLRVDPQERVVALADPRMLEAPFCYLAGHTLVEFNAAERQNFVRYVRNGGFVFVDDCNHDIDGLFATSFEAQMGRLFGPKALQKLPNSHALYRSFFRFPDGPPATSFELNGWGDDLVHDYLKGIEVDGRLGLLYSNKDYGCEWDYDWRNKRFLAEDNTRFGVNIVMHALNN
>NZ_CP040429.1|WP_025876012.1|121763_123098_-|TldD/PmbA-family-protein
MSIFTEAQAKAILDKVIALSKADECTAVLAGSINGNIRFALNNVSTSGIVDNTELAVTVAFGKRVGTASINEFDDAALQRVVRRAEDLARLAPENPEFMPAIGKQTYRPSPTFSESTAAIDPAFRAKVAADSIAPCRGNGLIAAGFLEDGQGFYATANSNGNFGYQRTTNFDYTCTVRTEDGRGSGWVGRNLKDAADFKADQDIRIAMRKATESQEAKALEPGKYTVILEPAAAAGLISFMMNFFSARSADEGRSFLSKKGGGNKLGEQVYDPRVNMHADPWHPDAPVLPWDNEGMPRERIAIIENGKVANLDYSRFWAQKQGKTAKATPGNLLMSGGEKSTAELVRGTQKGILVTRTWYIRMVDPQTVLLTGLTRDGTFYIENGQIKHPVKNFRFNESPVIMLNNIEELGKPVRVAGDESNFVMMIPPMKLRDFTFTSLSDAV
>NZ_CP040429.1|WP_154878990.1|123119_124754_-|TldD/PmbA-family-protein
MHRRDFLALTGLTAGGLIVPSFFGKAIAAEQLQSSLDPALKKRLADAALQAARSAGATYCDVRIGRYLRQFVITREDKVQNVVNTESTGVGIRVIVNGAWGFAATNALSTADVARAAQQAAAIAKANAGVQTAPVQLAKAPGVGEVSWKTPIRKNAMEVPIKEKVDLLLDVNAAAMGAGASFVNSMLFLVNEQKYFASTDGSYIDQDVHRIWAPMTITAIDKASGKFRTREGLSAPMGLGYEYLDGAATGKVLTPNGVVNYGSSYDMKEDAIAAAKQAQEKLKAPSVKPGKYDLILDPSHTWLTIHESIGHPLELDRVLGYEANYAGTSFATLDKREQHFQYGSDKVNIFADKTQPGSLGAVAYDDEGVKCKRWDLISNGKLVDYQTIRDQAHILGKTESDGCCYADSWSSVQFQRMANVSMAPGKSPLSVSDMIKDVENGIYIIGDGSFSIDQQRYNAQFGGQLFYEIKNGKITRMLEDVAYQIRTPEFWNACSAVADERDYRLGGSFFDGKGQPGQVSAVSHGSSTARFNGINVINTARSLG
>NZ_CP040429.1|WP_154881297.1|124781_126365_-|TldD/PmbA-family-protein
MALPHSRLIAAEQLLAPVDPAKRRRLAEVALAAARSAMASYCDVRIGRYLNQSVITREHQVGNVTNRESSGVGVRVIVNGAWGFAATHQQTEAAVRTAVEQATAIARANASIQSRPVQLAPTPAVGEVRWQTPIRRNAMEVPIQDKIELLLALNAAALNAGADYINSTLFLVNEQKYFASSDGSFIDQDIHRIWLPFTATAIDKASGKFRTRAGLSSPMGMGYEFLDGDARGKVQLPGGITAYRDSYDPVEDAIAAARQAREKLKAPSVKPGKYDLVLDPSNLFLTIHENVGHPLELDRVLGYEANYAGTSFATLDKRDAGFRWGSDIVTFFADKTQPGSLGAVGYDDEGVKTQRWDLVRDGILVDYQATRDEAHILGRDASHGCSYADSWSSVQFQRMANVSLAPGRTPLSVEDMIKDVENGIYIHGRGSYSIDQQRYNAQFGGQLYYQIRNGKITGMVEDAAYQIRTPEFWNACTAICDERDFRLGGSFFDGKGQPGQVSAVSHGSSTTRFNGINIINTARSLGA
>NZ_CP040429.1|WP_080150268.1|127189_127804_+|DUF938-domain-containing-protein
MSSKPYSEACERNREPIAAALDPWMGDRHRVLEIGSGTGQHAAFFAERWPWLRWQPSDHPDHLPGIESWRAEAALLNLLPPVALQVELPPAPGLSLPEGSTFDAAFSANTLHIMSWEHVQALFAALPPLLRHGALLAVYGPFNYGGRYTSDSNAQFDAWLKARDPRSGIRDSEAVQALAADNGFTRLGDVAMPSNNRLLLWRLG

Crispr_ID: NZ_CP040429_3

• CRISPR_ID: NZ_CP040429_3
• CRISPR_location: 393331-393412
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_3

Consensus_repeat	Method
GCCGCCGTTGACGGTCTCGATGCTGCC	CRISPRCasFinder

spacers of NZ_CP040429_3

>3.1|393358|27|NZ_CP040429|CRISPRCasFinder
GCGCACGCGGCTGCCGACCAGGCCGAT

CRISPR arrays and Neighbor proteins around NZ_CP040429_3

CRISPR arrays

The CRISPR arrays of NZ_CP040429_3

>merge|NZ_CP040429|3|393331-393412|CRISPRCasFinder
GTCGCCGTTGACGGTCTCCACGTCCTTGCGCACGCGGCTGCCGACCAGGCCGATGCCACCGTTGACGGTTTCCACGCCGCCT

>NZ_CP040429|3|3|393331-393412|CRISPRCasFinder
GTCGCCGTTGACGGTCTCCACGTCCTT	GCGCACGCGGCTGCCGACCAGGCCGAT
GCCACCGTTGACGGTTTCCACGCCGCCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase	unknown	unknown	gnl|CDD|236579
NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein	unknown	unknown	gnl|CDD|367457
NZ_CP040429.1|WP_025879428.1|375158_375389_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|223777
NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|227278
NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II	unknown	unknown	gnl|CDD|259979
NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter	unknown	unknown	gnl|CDD|377432
NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|273670
NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP040429.1|WP_025879423.1|371462_372137_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase	unknown	unknown	gnl|CDD|235645
NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA	unknown	unknown	gnl|CDD|237017
NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein	unknown	unknown	gnl|CDD|378350
NZ_CP040429.1|WP_005407770.1|371194_371287_-|potassium-transporting-ATPase-subunit-F	unknown	unknown	unknown
NZ_CP040429.1|WP_051501537.1|399270_399711_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase	unknown	unknown	gnl|CDD|349910
NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|236946
NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter	unknown	unknown	gnl|CDD|341039
NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase	unknown	unknown	gnl|CDD|223864
NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197336

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase	gnl|CDD|236579	PRK09585, anmK, anhydro-N-acetylmuramic acid kinase; Reviewed.	0
NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II	gnl|CDD|259979	cd13912, CcO_II_C, C-terminal domain of Cytochrome c Oxidase subunit II. Cytochrome c Oxidase (CcO), the terminal oxidase in the respiratory chains of eukaryotes and most bacteria, is a multi-chain transmembrane protein located in the inner membrane of mitochondria and the cell membrane of prokaryotes. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. The number of subunits varies from three to five in bacteria and up to 13 in mammalian mitochondria. Only subunits I and II are essential for function. Subunits I, II, and III of mammalian CcO are encoded within the mitochondrial genome and the remaining 10 subunits are encoded within the nuclear genome. Subunit II contains a copper-copper binuclear site called CuA, which is believed to be involved in electron transfer from cytochrome c to the binuclear center (active site) in subunit I.	2.52721e-70
NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease	gnl|CDD|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	8.47073e-28
NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|227278	COG4942, COG4942, Membrane-bound metallopeptidase [Cell division and chromosome partitioning].	8.21394e-87
NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter	gnl|CDD|377432	pfam04973, NMN_transporter, Nicotinamide mononucleotide transporter. Members of this family are integral membrane proteins that are involved in transport of nicotinamide mononucleotide.	4.01449e-49
NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase	gnl|CDD|273670	TIGR01526, nadR_NMN_Atrans, nicotinamide-nucleotide adenylyltransferase, NadR type. The NadR protein of E. coli and closely related bacteria is both enzyme and regulatory protein. The first 60 or so amino acids, N-terminal to the region covered by this model, is a DNA-binding helix-turn-helix domain (pfam01381) responsible for repressing the nadAB genes of NAD de novo biosynthesis. The NadR homologs in Mycobacterium tuberculosis, Haemophilus influenzae, and others appear to lack the repressor domain. NadR has recently been shown to act as an enzyme of the salvage pathway of NAD biosynthesis, nicotinamide-nucleotide adenylyltransferase; members of this family are presumed to share this activity. E. coli NadR has also been found to regulate the import of its substrate, nicotinamide ribonucleotide, but it is not known if the other members of this model share that activity.	1.62052e-39
NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	1.78761e-82
NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	3.24982e-131
NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase	gnl|CDD|235645	PRK05912, PRK05912, tyrosyl-tRNA synthetase; Validated.	0
NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA	gnl|CDD|237017	PRK11904, PRK11904, bifunctional proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase PutA.	0
NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein	gnl|CDD|378350	pfam10003, DUF2244, Integral membrane protein (DUF2244). This domain, found in various bacterial hypothetical and putative membrane proteins, has no known function.	2.53184e-28
NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein	gnl|CDD|367457	pfam03349, Toluene_X, Outer membrane protein transport protein (OMPP1/FadL/TodX). This family includes TodX from Pseudomonas putida F1 and TbuX from Ralstonia pickettii PKO1. These are membrane proteins of uncertain function that are involved in toluene catabolism. Related proteins involved in the degradation of similar aromatic hydrocarbons are also in this family, such as CymD. This family also includes FadL involved in translocation of long-chain fatty acids across the outer membrane. It is also a receptor for the bacteriophage T2.	2.26802e-120
NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|236946	PRK11649, PRK11649, putative peptidase; Provisional.	2.67753e-53
NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter	gnl|CDD|341039	cd17486, MFS_AmpG_like, AmpG and similar transporters of the Major Facilitator Superfamily. AmpG acts as an inner membrane permease in the beta-lactamase induction system and in peptidoglycan recycling. It transports meuropeptide from the periplasm into the cytosol in gram-negative bacteria, which is essential for the induction of the ampC encoding beta-lactamase. The AmpG family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.69727e-107
NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase	gnl|CDD|349910	cd05660, M28_like_PA, M28 Zn-peptidase containing a protease-associated (PA) domain insert. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions. This subfamily is composed of uncharacterized proteins containing a protease-associated (PA) domain insert which may participate in substrate binding and/or promote conformational changes, influencing the stability and accessibility of the site to substrate.	1.68749e-113
NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III	gnl|CDD|197336	cd10281, Nape_like_AP-endo, Neisseria meningitides Nape-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Neisseria meningitides Nape and related proteins. These are Escherichia coli exonuclease III (ExoIII)-like AP endonucleases and 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 efficiences. 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. Nape, found in this subfamily, is the dominant AP endonuclease. It exhibits strong AP endonuclease activity, and also exhibits 3'-5'exonuclease and 3'-deoxyribose phosphodiesterase activities.	5.44785e-146

Protein sequences

>NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase
MPRKLLLCLAAAAALSACKGEDTPAPAPSVDSAAKPATHTFSAAINAADFAEMVKTLASDEFEGRSPGSKGEELTVNYIRDQMQRIGLQPGNGDSWFQDVPMTETTADESTVLTLTQGGKTRELKFGTDMVVGTRTGQTEVKVDASDLVFVGYGVDAPEQKWNDYAGQDWKGKTVVMFVNDPGFHVDDEKLFDGKRMTYYGRWTYKFEEAARKGAAAALIVHDTAGASYGWDVVKNSWAGPQYDLPAKDDAEPRLPVQGWLSADAAKALFAGAGLDLDQAYKDASKPGFKPVPLKATASVDLKSKVAQKQSRNVVGVLPGSKRADEAVLYMAHWDHLGKHEGEQGDNIYNGAVDNATGVAGILEVAEAMAHQEPKPERSVVFLAVTLEESGLLGSKYYVAHPTFPLDKIAGVINIDAMSVAGRAKDVTVTGFGSSELEDILKPLAAAQDRTLHGETSVQSGFYFRSDHFNFAKAGVPALYADGGEDLRDGGVEAGRKAAADYGSNRYHGPKDEYDPATWKLDGTVEDLQLMYGVGKELAGGDRWPNWYEGNPFKAARDTMMKAKAPAAAAK
>NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase
MSSIEEALALIGRGADEILKLEDLRARLQEGRPLRIKAGFDPTAPDLHLGHTVLLNKMRQFQDLGHQVIFLIGDFTGMIGDPSGKSLTRKPLSRDDVLANARTYEEQVFKVLDRSRTEVRFNSEWFGKMSAADMIRLAGQHTVARMLERDDFAKRYAAQQSIAIHEFLYPLVQGYDSVALEADVELGGTDQKFNLLMGRGLQEHHGQKPQVVLTMPLLEGLDGVNKMSKSLGNYIGISEPAIDIVTKTMKVDDALMWRWIELLSFDISQAEAASLREQIAAGLNPRVVKLRLARELATRFHDAAAAEQAIAGWEAAVTGQGDITQLPLQDVAIPAEGLRIAALLTAAGLTPSNSEANRKLKERAVKVDGEVVEDGQQVLQPGFEGLLQVGKRTFARVRLIAA
>NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MLNSDQGRARKQRFQERLHVLHDNALHRKLRQHLPAAFNERWTRRHWMHASLFVTIGALVATIVPGFSHTIDAPYADSHTSLALPLPPLAMARQQQIPGDSWQVLRVQRGQTLSDLFDKAGISATTLHRVLDHPGARESLTKLRPGAEIAFDMPLSGDLRSIRFDRDADNRVELSLSGDDIKETVTKRETSTRTVVTSGEITSSLYAAARRAGLSPSAIATMTDDIFKYDIDFSKDLQPGDRFSVVMDETWREGEKVDTSKILAATFTTGGKTYSGFRFDRNGKSEYYDISGRSLKKSFIRMPIPFARLSSTFGARKHPVLGKMRMHKGVDYAARTGTPIMAAGDARVQFVGVQRGYGNVVILDHGRGHTTLYGHMSRFAGIKNGQRVAQGTVIGYVGSTGLATGPHLHYEFRVNGEHRNPLTVTMPPPEPLKGAELVAFRAQTAPAMARIQGMEKLIYADASPAPAAESASTEVASAKDKAPAGRKRG
>NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase
MNTTADPSLPLYLGLMSGTSADGIDAALVQFPADGGCRFVHGLTARWEPVLRARLVALGEGGPLQSLEELGELDARIAISFAAAANQLLEEAGVDRSQVRAIGSHGQTVRHRPLADPAFTVQLGDGNRIAELTGITTVCDFRRRDVAAGGHGAPLMPAFHLDMLGAADEDRAVLNLGGIANLTLIPREGVVRGFDTGPANALMDAWCQRHTGRSFDADGAYAASGAVDDSLLAGWRADPWFALPPPKSTGREQFHLPWAEAHMEEGQFAAADVQATLLELTAATVVDALLAQQPHTRRVLVCGGGVRNTQLMRRLAARLPGVVVESTALHGLDPEYVEAMGFAWLAQRTMDGLPGNLPSVTGATGPRILGAIHPA
>NZ_CP040429.1|WP_025879428.1|375158_375389_+|hypothetical-protein
MADVVLRDLDPLLLERIKRVSVARGWTHEQTCAVLLEQGLFSSELEVRSGFGDPEVDALSDAIAALQALPAGQGFD
>NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter
MTEAAKPAGYKGWAGIKRAFGTPSALTMALLGFGSGLPFLLIASQTLSTRLRDVGLDLGSIGLISLASFFYLLKFVWAPLLDRYAFPLLGFLGRRRSWLLVSQILVLVGLVALAFVRPEQGVWPLVAWVLVASFAGATQDSVVDAYRIEIAPQTAQAALAATYTLGYRIGLILAGAGALYLAQFEGWIIAYLAMAALMILPIITTLFCREPERPANAVQRRIDIAEAFVQPITSFFTRNGMALALALLAFVGFFKFPDQVIGVMAGPFYLDSGFDKADIATVSKLFGVWMGIGGAFLGGIAVAAFGFRRMLLVAALGVALSNLAFLLMAHNPGQLWAFYAALSADNLFQGFAGTVLVAFMSSLTDRNFTATQYALLVSLANLPGKFVGGVSGYIVEATSYSTFFMLSAVTVVPTMLLLAWLWPRIVDRGPSPAA
>NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III
MRIISFNANGIRSAATKGFLDWFRGQDADVLCIQETKAQEDQLTDPMFRPDGHHCFYRDAITKKGYSGVAIYSKREPDQVITSLGWAPFDDEGRYIEARFGNLSVVSFYIPSGSSGDLRQGFKFEVMEWLRPILEEWARSGRDYVLCGDWNIVRSALDIKNWKSNQKNSGCLPEERDWLNALCADHGQATDVGAGRGWADAYRLLNPTGEDYTWWSNRGAARANNVGWRIDYQFITPGLRDHLRSCSIYRDQRFSDHAPFIVDYDL
>NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase
MSDHRHRFLQLALTADALRFGQFTLKSGRLSPYFFNAGRFDSGSLLSQLGACYSDAIDATGIKYDVVFGPAYKGIPLATAMACELAQRGRDLPLSFNRKEVKDHGEGGQLIGADMTGKRVLIVDDVITAGTAIREALAIIRAAGGIPAGIVVALDRQEIASDSDHRSAAQAVAEEAGIPVIAVATLADLLDFASGNPELVGYRQPLEAYRAQYGVRSTR
>NZ_CP040429.1|WP_025879423.1|371462_372137_-|hypothetical-protein
MFRVPAIVAASLLLVMPQTLLAQSSGKAADKKLYCWNEGKERICSDALPADAVNHARDEFSANSGLRNAQVQRALSDEERAAASTAAAQVQLDQMAEQTRQRTEQAMLTTYGDENALRRVFAERQEVLDNNLKTAQYNVASLRESLVALLAAAGDRELAGGKVADKQAQAIGQRHAQLQSQQRLLASFEQQQQALKVEIESSLQRYRQLKGLAPVDVPAQTPAG
>NZ_CP040429.1|WP_005407770.1|371194_371287_-|potassium-transporting-ATPase-subunit-F
MSPWLSLLCGVLVLVAAAYLLYVVLRPESF
>NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein
MRNNVFPSRRHHIATLRGGRCLLLGMALALALPLPGAAQTSSAREAERKLQKLRTELKGVAQERRQIEGQRGQASQQLREADEKVARSGRALAQTESALREQTQALAQAEQRRNALQSNLEKQNRELAGLLRAAYQLGNHAPLKLLLSQDTVADANRALAYHRYLQRERAQRITTLTADLKELETLQAQIAQRQQQLQGTHRDQKQQVATLASDRRERAQTVASLEERFKDKREKEQALGQDAKALETLLANLRAAAARAEAERRAAARKAAAEKAAAEKAARQAKAEGRPAPATKIPPAVASAPAPKVGGLGWPLSGNLLARYGGKLPDGRTSSGVLIGAPAGSTVTAVADGTVVFSDWMTGYGMILIVDHGNGYMSLYAHNDTLLKDAGARVSRGDAVAKVGNSGGQGVTALYFELRRGGQPVNPDSWLQRR
>NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase
MRAARTATLLLALLPALSWAQQTAPVPLKETPGKAASSEEAVTSKVPLDDIRRFVAVYNAVRAAYVDPVDDNKLMQSAVRGLLLDLDPHSTYFNKEDAEAFDEQANGAYEGIGVELQQQPDNASMKVISPIDDTPAAKAGILAGDLIIAIDGKPISAIDASEPLRGPAGSKVVLTIVRDGKPKPFDVSLTRQTIRVTSVRSRLLEPGYGYIRLSTFQADTGSDFQKHLQQLQKQSGGNLKGLVLDLRSNPGGLLTAAVQVADDLLDKGNIVSTRGRISISDARFDATPGDLLKGAPVVVLVDAGSASASEVLAGALRDNKRARVIGSRTFGKGSVQTVLPLDNGDSVKLTTARYYTPSGKSIQATGIVPEVELKAAPRPEDEALPASLSDYSEATLPGHLRGDEEGTEGYHAGAVLPGDGPINDALAELKNPGSVAARLKAEAAKAEADRAAKAAAKPAPKAEPKAEAKPEAKPEAKPEAKPAEIPAKP
>NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease
MFVSLPSRKKATLRWATPVLFAALWLAFLWSISRPDDARGSLWLDWGALSTGLTHPLDWWATLQDGSVLRLFTALFLHADWSHLLGNLVFLLIFGLPAERVLGPWRLLLLFLVGGAISNLVAIYTMGSPDQIIIGASGAVSALIGAYLALFPGARLGVVIPLGLFLEFVRAPAYLLIGVWAALQVVFAYIGPTFGMVAWWAHIGGFVFGVVYGMYVRAAIARRLRKRHGF
>NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein
MQTASTIARLTLLAVGVAGALAAADANAAAFQLKENSAKGLGRAFAGSTSAEGDASVVATNPASMRLLEGTQIQGDVSAISFGAKFRGEGRYANGAPISGGNGGDAGMIAPVPAAYFHVPFGEKDNMHFGVSLTVPFGFKTEYDRDWVGRYNGVKTELQAIDLGAAFSYDVNPYLSFGASVFAERLNVDLTSAVDGGTAINASAQQRAAAAALAAGRTPAQAQAAAQAAGRQAAQLGFSPGTADGYLRIKGDEVSVGYTLGMTVSPVEGTNIAFSYRSEVEHKITDGKADFTMTPAAAAFLAQAAPGTFVDSNGRATITLPASATVSFTHRVNDQWKIMADVSRTAWSKFDEVRVDYDSNQPDSVLPFHYRDTTFASIGTEYRLNEQLTLRGGLAYDQTPTTDAHRDVRVPDTTRKWLSLGLTWAPSEKMEYSVGYTHLFTKDPNINSTSATANNVVGKYKVTGDVLAASMQYKF
>NZ_CP040429.1|WP_051501537.1|399270_399711_+|hypothetical-protein
MADRRYLKKMTRYWAAEEARATVALQDALASEWFDYWHTHLDWKGRGNRHGSDRTAVAAALLRLLERAVACRRQDTQCWVVLAPDSGQSALFLHSPNPQGTPWPHPFDGVTWDIEAPDWLAPVMAPHHQLGRWGSAEPRLLVRVRA
>NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter
MNLSDPNFQLELAANIAVAGSILLAGRNNVHTWWLGIVGCALFAAVFERSHLYADMVLQFFFVVISVFGWWQWLRGDHGAPLPITRLPARAWSWLLPLAVLATFGYGWMLTRLTNAYAPYIDSAVLVLSVIAQILMMRRKLESWWVWLLVNTIAVPLYYSRGLHLTSILYVGFWINALVALRHWRHLMRAEADTGRAADGIA
>NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase
MALPERVPRGLVVGKFCPLHLGHERLMEFASTRCTQLLVIGWSQPGFAGYSAARRERWLRARFPQATVAVLDDARLAALCRQQGVPVRALPQDKDSEQVQRAFTAWLCVALFGGPVQAVFTGEDYGDGFAAALAQHFNAPVQHHRLERSTDIGQASGTELRADPHAHRQGLSRSVYADHVQRVAFIGGESTGKSTLARVLAERQGTAWVPEFGRTLWEQQGGELQAQDLLRIAATQPQHEHQAAQHAHRWLFCDTTPLVTLGYSGWMFGTAPEPLQRAAARAYDLLFLCAPDIPFEQDGTRVGEEFRMRQHAWYLQQLQARGMAYVLLEGDLEMRIARVLEELVRRADNRFSVLAESVARGWQARIRPT
>NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA
MNAPSSPIAASDAPRPSALLSPELPASPNPFRQAITDGWLKDEASHVRELLAQARLPADEQAKVQALAADLVARVRVRAKDQGAIEAFMRQYDLGSEEGVLLMCVAEALLRIPDQETADKLIRDKLADADWEKHLGGSDSVLVNASTWGLMLTGKLVQMNDATRADAPSAFKRLVGRVGEPVVRLAVRQAMKIMGHQFVMGRTIGEALARSHKGDSASYRYSFDMLGEGALTMKDALRYLEDYRRAIHAIGGDHKARGGRADGDVNNAPGISIKLSALYPRYEHAKRARVLKDLVPGVLELAQLAKSYGIGCTVDAEESDRLELSLDIIEQVFGDASLAGWDGFGVVVQAYQKRTPYTIDHLADMARRAGRRLQVRLVKGAYWDAEIKRAQIEGYAGYPVFTRKQNTDVSYLACAKRLFTHADAIYPMFATHNAHTIAAVRSIANGGVYEHQKLHGMGDDLYAEVVPADRLGLPCRVYAPVGSHEDLLPYLVRRLLENGANSSFVNRITDERVPIADLVRDPVEMVSSFESIPHPKIPLPVDLLRSQNHDRKNSMGANLANDNELRALAEQLNAAVKPWQAAPLVPGADPTGASLPVTNPADTREVVGQWQAADAATVQKALANAVAAQPAWNRTPAASRAAILEHAADQLEARMPEFMALCVKEAGKSLPDGIAEVREAVDFLRYYAKQAREQFSHAEKLPSPTGESNELQLHGRGVFVCISPWNFPLAIFLGQVAAALAAGNSVIAKPAEQTNLIGYYAVKLLHDAGVPADVVQYLPGDGATVGAALTADPRVAGVAFTGSTDTARAINRAMAARDAAIGVLIAETGGQNAFIADSSALPEQLVKDAIGSAFTSAGQRCSAARVLFVQDDIADKVMTMLAGAMKELKVGNPGLLSTDVGPVIDADALKILQDHAVRMDREARLIAAAELSAEAANGTFFAPRAYELKDLGKLQKEIFGPVLHVIRWKGDQLDAVIDQINATGYGLTLGVHSRIDETVDRISNGVHVGNVYVNRNQIGAVVGVQPFGGQGLSGTGPKAGGPHYLLRFATEKTVTVNTTAAGGNASLLTLGD
>NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein
MIEVLTAPDGSGTQLRLRPPRALDARQFVLLFAVLSGVMWLVSAFGWVAGNAFAPLFALLYSLLLAAALRALWRSGERQEEIRVVPACVEVIPVPGGSPVFRAHPHWVRLLTDDQRVRLASSGRQVEVGSFLAPAERQTLVETLEDLLAASDGGNRRR
>NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II
MKQSRGWGTKCVAMAAAMGALLSMPGTVLAQAADPKPWQLNMGKGVTQTSRLAWESNNLSLIVCTVIGVIVFGAMAYAMFKFRKSKGAVAATFSHNTKAEVIWTVIPVIILVVMAWPATANLIKMYDTRDAEMTVKVTGYQWMWKYEYLGENVTFTSRLDRESDRMRQSGKVPTRESHPHYLLDVDNRLVLPVDTKVRFVITSDDVIHAWWVPALGWKQDAIPGFINEAWTSIEQPGVYRGQCAELCGKDHGFMPIVVEAVSKEEFKQWLAQRKPAPAPAAPAAPAEPTAPASETPAQPAAPAAAEAGNAPAAAASGA

Crispr_ID: NZ_CP040429_4

• CRISPR_ID: NZ_CP040429_4
• CRISPR_location: 393499-393633
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP040429_4

Consensus_repeat	Method
GCCGCCGTTGACGGTCTCGATGCTGCC	CRISPRCasFinder

spacers of NZ_CP040429_4

>4.1|393526|27|NZ_CP040429|CRISPRCasFinder
CGTGCGCGCACGATCGGCGACCTTGAC
>4.2|393580|27|NZ_CP040429|CRISPRCasFinder
GGTTTCCACGCCTTCGCCGACACGGAT

CRISPR arrays and Neighbor proteins around NZ_CP040429_4

CRISPR arrays

The CRISPR arrays of NZ_CP040429_4

>merge|NZ_CP040429|4|393499-393633|CRISPRCasFinder
GCCGCCGTTGACGGTCTCGATGCTGCCCGTGCGCGCACGATCGGCGACCTTGACGCCGCCGTTGACGGTGTCGATGCTGCCGGTTTCCACGCCTTCGCCGACACGGATGCCACCATTGACGGTGTCCAGCTTGCC

>NZ_CP040429|4|4|393499-393633|CRISPRCasFinder
GCCGCCGTTGACGGTCTCGATGCTGCC	CGTGCGCGCACGATCGGCGACCTTGAC
GCCGCCGTTGACGGTGTCGATGCTGCC	GGTTTCCACGCCTTCGCCGACACGGAT
GCCACCATTGACGGTGTCCAGCTTGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase	unknown	unknown	gnl|CDD|236579
NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein	unknown	unknown	gnl|CDD|367457
NZ_CP040429.1|WP_025879428.1|375158_375389_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|223777
NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|227278
NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II	unknown	unknown	gnl|CDD|259979
NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter	unknown	unknown	gnl|CDD|377432
NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|273670
NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP040429.1|WP_025879423.1|371462_372137_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase	unknown	unknown	gnl|CDD|235645
NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA	unknown	unknown	gnl|CDD|237017
NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein	unknown	unknown	gnl|CDD|378350
NZ_CP040429.1|WP_005407770.1|371194_371287_-|potassium-transporting-ATPase-subunit-F	unknown	unknown	unknown
NZ_CP040429.1|WP_051501537.1|399270_399711_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase	unknown	unknown	gnl|CDD|349910
NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|236946
NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter	unknown	unknown	gnl|CDD|341039
NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase	unknown	unknown	gnl|CDD|223864
NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197336

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase	gnl|CDD|236579	PRK09585, anmK, anhydro-N-acetylmuramic acid kinase; Reviewed.	0
NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II	gnl|CDD|259979	cd13912, CcO_II_C, C-terminal domain of Cytochrome c Oxidase subunit II. Cytochrome c Oxidase (CcO), the terminal oxidase in the respiratory chains of eukaryotes and most bacteria, is a multi-chain transmembrane protein located in the inner membrane of mitochondria and the cell membrane of prokaryotes. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. The number of subunits varies from three to five in bacteria and up to 13 in mammalian mitochondria. Only subunits I and II are essential for function. Subunits I, II, and III of mammalian CcO are encoded within the mitochondrial genome and the remaining 10 subunits are encoded within the nuclear genome. Subunit II contains a copper-copper binuclear site called CuA, which is believed to be involved in electron transfer from cytochrome c to the binuclear center (active site) in subunit I.	2.52721e-70
NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease	gnl|CDD|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	8.47073e-28
NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|227278	COG4942, COG4942, Membrane-bound metallopeptidase [Cell division and chromosome partitioning].	8.21394e-87
NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter	gnl|CDD|377432	pfam04973, NMN_transporter, Nicotinamide mononucleotide transporter. Members of this family are integral membrane proteins that are involved in transport of nicotinamide mononucleotide.	4.01449e-49
NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase	gnl|CDD|273670	TIGR01526, nadR_NMN_Atrans, nicotinamide-nucleotide adenylyltransferase, NadR type. The NadR protein of E. coli and closely related bacteria is both enzyme and regulatory protein. The first 60 or so amino acids, N-terminal to the region covered by this model, is a DNA-binding helix-turn-helix domain (pfam01381) responsible for repressing the nadAB genes of NAD de novo biosynthesis. The NadR homologs in Mycobacterium tuberculosis, Haemophilus influenzae, and others appear to lack the repressor domain. NadR has recently been shown to act as an enzyme of the salvage pathway of NAD biosynthesis, nicotinamide-nucleotide adenylyltransferase; members of this family are presumed to share this activity. E. coli NadR has also been found to regulate the import of its substrate, nicotinamide ribonucleotide, but it is not known if the other members of this model share that activity.	1.62052e-39
NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	1.78761e-82
NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	3.24982e-131
NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase	gnl|CDD|235645	PRK05912, PRK05912, tyrosyl-tRNA synthetase; Validated.	0
NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA	gnl|CDD|237017	PRK11904, PRK11904, bifunctional proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase PutA.	0
NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein	gnl|CDD|378350	pfam10003, DUF2244, Integral membrane protein (DUF2244). This domain, found in various bacterial hypothetical and putative membrane proteins, has no known function.	2.53184e-28
NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein	gnl|CDD|367457	pfam03349, Toluene_X, Outer membrane protein transport protein (OMPP1/FadL/TodX). This family includes TodX from Pseudomonas putida F1 and TbuX from Ralstonia pickettii PKO1. These are membrane proteins of uncertain function that are involved in toluene catabolism. Related proteins involved in the degradation of similar aromatic hydrocarbons are also in this family, such as CymD. This family also includes FadL involved in translocation of long-chain fatty acids across the outer membrane. It is also a receptor for the bacteriophage T2.	2.26802e-120
NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|236946	PRK11649, PRK11649, putative peptidase; Provisional.	2.67753e-53
NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter	gnl|CDD|341039	cd17486, MFS_AmpG_like, AmpG and similar transporters of the Major Facilitator Superfamily. AmpG acts as an inner membrane permease in the beta-lactamase induction system and in peptidoglycan recycling. It transports meuropeptide from the periplasm into the cytosol in gram-negative bacteria, which is essential for the induction of the ampC encoding beta-lactamase. The AmpG family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.69727e-107
NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase	gnl|CDD|349910	cd05660, M28_like_PA, M28 Zn-peptidase containing a protease-associated (PA) domain insert. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions. This subfamily is composed of uncharacterized proteins containing a protease-associated (PA) domain insert which may participate in substrate binding and/or promote conformational changes, influencing the stability and accessibility of the site to substrate.	1.68749e-113
NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III	gnl|CDD|197336	cd10281, Nape_like_AP-endo, Neisseria meningitides Nape-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Neisseria meningitides Nape and related proteins. These are Escherichia coli exonuclease III (ExoIII)-like AP endonucleases and 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 efficiences. 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. Nape, found in this subfamily, is the dominant AP endonuclease. It exhibits strong AP endonuclease activity, and also exhibits 3'-5'exonuclease and 3'-deoxyribose phosphodiesterase activities.	5.44785e-146

Protein sequences

>NZ_CP040429.1|WP_033830160.1|391296_393012_-|M28-family-peptidase
MPRKLLLCLAAAAALSACKGEDTPAPAPSVDSAAKPATHTFSAAINAADFAEMVKTLASDEFEGRSPGSKGEELTVNYIRDQMQRIGLQPGNGDSWFQDVPMTETTADESTVLTLTQGGKTRELKFGTDMVVGTRTGQTEVKVDASDLVFVGYGVDAPEQKWNDYAGQDWKGKTVVMFVNDPGFHVDDEKLFDGKRMTYYGRWTYKFEEAARKGAAAALIVHDTAGASYGWDVVKNSWAGPQYDLPAKDDAEPRLPVQGWLSADAAKALFAGAGLDLDQAYKDASKPGFKPVPLKATASVDLKSKVAQKQSRNVVGVLPGSKRADEAVLYMAHWDHLGKHEGEQGDNIYNGAVDNATGVAGILEVAEAMAHQEPKPERSVVFLAVTLEESGLLGSKYYVAHPTFPLDKIAGVINIDAMSVAGRAKDVTVTGFGSSELEDILKPLAAAQDRTLHGETSVQSGFYFRSDHFNFAKAGVPALYADGGEDLRDGGVEAGRKAAADYGSNRYHGPKDEYDPATWKLDGTVEDLQLMYGVGKELAGGDRWPNWYEGNPFKAARDTMMKAKAPAAAAK
>NZ_CP040429.1|WP_154879157.1|378305_379514_+|tyrosine--tRNA-ligase
MSSIEEALALIGRGADEILKLEDLRARLQEGRPLRIKAGFDPTAPDLHLGHTVLLNKMRQFQDLGHQVIFLIGDFTGMIGDPSGKSLTRKPLSRDDVLANARTYEEQVFKVLDRSRTEVRFNSEWFGKMSAADMIRLAGQHTVARMLERDDFAKRYAAQQSIAIHEFLYPLVQGYDSVALEADVELGGTDQKFNLLMGRGLQEHHGQKPQVVLTMPLLEGLDGVNKMSKSLGNYIGISEPAIDIVTKTMKVDDALMWRWIELLSFDISQAEAASLREQIAAGLNPRVVKLRLARELATRFHDAAAAEQAIAGWEAAVTGQGDITQLPLQDVAIPAEGLRIAALLTAAGLTPSNSEANRKLKERAVKVDGEVVEDGQQVLQPGFEGLLQVGKRTFARVRLIAA
>NZ_CP040429.1|WP_025879426.1|376668_378138_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MLNSDQGRARKQRFQERLHVLHDNALHRKLRQHLPAAFNERWTRRHWMHASLFVTIGALVATIVPGFSHTIDAPYADSHTSLALPLPPLAMARQQQIPGDSWQVLRVQRGQTLSDLFDKAGISATTLHRVLDHPGARESLTKLRPGAEIAFDMPLSGDLRSIRFDRDADNRVELSLSGDDIKETVTKRETSTRTVVTSGEITSSLYAAARRAGLSPSAIATMTDDIFKYDIDFSKDLQPGDRFSVVMDETWREGEKVDTSKILAATFTTGGKTYSGFRFDRNGKSEYYDISGRSLKKSFIRMPIPFARLSSTFGARKHPVLGKMRMHKGVDYAARTGTPIMAAGDARVQFVGVQRGYGNVVILDHGRGHTTLYGHMSRFAGIKNGQRVAQGTVIGYVGSTGLATGPHLHYEFRVNGEHRNPLTVTMPPPEPLKGAELVAFRAQTAPAMARIQGMEKLIYADASPAPAAESASTEVASAKDKAPAGRKRG
>NZ_CP040429.1|WP_080277682.1|375476_376604_-|anhydro-N-acetylmuramic-acid-kinase
MNTTADPSLPLYLGLMSGTSADGIDAALVQFPADGGCRFVHGLTARWEPVLRARLVALGEGGPLQSLEELGELDARIAISFAAAANQLLEEAGVDRSQVRAIGSHGQTVRHRPLADPAFTVQLGDGNRIAELTGITTVCDFRRRDVAAGGHGAPLMPAFHLDMLGAADEDRAVLNLGGIANLTLIPREGVVRGFDTGPANALMDAWCQRHTGRSFDADGAYAASGAVDDSLLAGWRADPWFALPPPKSTGREQFHLPWAEAHMEEGQFAAADVQATLLELTAATVVDALLAQQPHTRRVLVCGGGVRNTQLMRRLAARLPGVVVESTALHGLDPEYVEAMGFAWLAQRTMDGLPGNLPSVTGATGPRILGAIHPA
>NZ_CP040429.1|WP_025879428.1|375158_375389_+|hypothetical-protein
MADVVLRDLDPLLLERIKRVSVARGWTHEQTCAVLLEQGLFSSELEVRSGFGDPEVDALSDAIAALQALPAGQGFD
>NZ_CP040429.1|WP_032977021.1|373776_375081_+|MFS-transporter
MTEAAKPAGYKGWAGIKRAFGTPSALTMALLGFGSGLPFLLIASQTLSTRLRDVGLDLGSIGLISLASFFYLLKFVWAPLLDRYAFPLLGFLGRRRSWLLVSQILVLVGLVALAFVRPEQGVWPLVAWVLVASFAGATQDSVVDAYRIEIAPQTAQAALAATYTLGYRIGLILAGAGALYLAQFEGWIIAYLAMAALMILPIITTLFCREPERPANAVQRRIDIAEAFVQPITSFFTRNGMALALALLAFVGFFKFPDQVIGVMAGPFYLDSGFDKADIATVSKLFGVWMGIGGAFLGGIAVAAFGFRRMLLVAALGVALSNLAFLLMAHNPGQLWAFYAALSADNLFQGFAGTVLVAFMSSLTDRNFTATQYALLVSLANLPGKFVGGVSGYIVEATSYSTFFMLSAVTVVPTMLLLAWLWPRIVDRGPSPAA
>NZ_CP040429.1|WP_033832834.1|372979_373780_+|exodeoxyribonuclease-III
MRIISFNANGIRSAATKGFLDWFRGQDADVLCIQETKAQEDQLTDPMFRPDGHHCFYRDAITKKGYSGVAIYSKREPDQVITSLGWAPFDDEGRYIEARFGNLSVVSFYIPSGSSGDLRQGFKFEVMEWLRPILEEWARSGRDYVLCGDWNIVRSALDIKNWKSNQKNSGCLPEERDWLNALCADHGQATDVGAGRGWADAYRLLNPTGEDYTWWSNRGAARANNVGWRIDYQFITPGLRDHLRSCSIYRDQRFSDHAPFIVDYDL
>NZ_CP040429.1|WP_025879424.1|372156_372816_-|orotate-phosphoribosyltransferase
MSDHRHRFLQLALTADALRFGQFTLKSGRLSPYFFNAGRFDSGSLLSQLGACYSDAIDATGIKYDVVFGPAYKGIPLATAMACELAQRGRDLPLSFNRKEVKDHGEGGQLIGADMTGKRVLIVDDVITAGTAIREALAIIRAAGGIPAGIVVALDRQEIASDSDHRSAAQAVAEEAGIPVIAVATLADLLDFASGNPELVGYRQPLEAYRAQYGVRSTR
>NZ_CP040429.1|WP_025879423.1|371462_372137_-|hypothetical-protein
MFRVPAIVAASLLLVMPQTLLAQSSGKAADKKLYCWNEGKERICSDALPADAVNHARDEFSANSGLRNAQVQRALSDEERAAASTAAAQVQLDQMAEQTRQRTEQAMLTTYGDENALRRVFAERQEVLDNNLKTAQYNVASLRESLVALLAAAGDRELAGGKVADKQAQAIGQRHAQLQSQQRLLASFEQQQQALKVEIESSLQRYRQLKGLAPVDVPAQTPAG
>NZ_CP040429.1|WP_005407770.1|371194_371287_-|potassium-transporting-ATPase-subunit-F
MSPWLSLLCGVLVLVAAAYLLYVVLRPESF
>NZ_CP040429.1|WP_025878307.1|393847_395152_+|peptidoglycan-DD-metalloendopeptidase-family-protein
MRNNVFPSRRHHIATLRGGRCLLLGMALALALPLPGAAQTSSAREAERKLQKLRTELKGVAQERRQIEGQRGQASQQLREADEKVARSGRALAQTESALREQTQALAQAEQRRNALQSNLEKQNRELAGLLRAAYQLGNHAPLKLLLSQDTVADANRALAYHRYLQRERAQRITTLTADLKELETLQAQIAQRQQQLQGTHRDQKQQVATLASDRRERAQTVASLEERFKDKREKEQALGQDAKALETLLANLRAAAARAEAERRAAARKAAAEKAAAEKAARQAKAEGRPAPATKIPPAVASAPAPKVGGLGWPLSGNLLARYGGKLPDGRTSSGVLIGAPAGSTVTAVADGTVVFSDWMTGYGMILIVDHGNGYMSLYAHNDTLLKDAGARVSRGDAVAKVGNSGGQGVTALYFELRRGGQPVNPDSWLQRR
>NZ_CP040429.1|WP_032975636.1|395259_396729_+|S41-family-peptidase
MRAARTATLLLALLPALSWAQQTAPVPLKETPGKAASSEEAVTSKVPLDDIRRFVAVYNAVRAAYVDPVDDNKLMQSAVRGLLLDLDPHSTYFNKEDAEAFDEQANGAYEGIGVELQQQPDNASMKVISPIDDTPAAKAGILAGDLIIAIDGKPISAIDASEPLRGPAGSKVVLTIVRDGKPKPFDVSLTRQTIRVTSVRSRLLEPGYGYIRLSTFQADTGSDFQKHLQQLQKQSGGNLKGLVLDLRSNPGGLLTAAVQVADDLLDKGNIVSTRGRISISDARFDATPGDLLKGAPVVVLVDAGSASASEVLAGALRDNKRARVIGSRTFGKGSVQTVLPLDNGDSVKLTTARYYTPSGKSIQATGIVPEVELKAAPRPEDEALPASLSDYSEATLPGHLRGDEEGTEGYHAGAVLPGDGPINDALAELKNPGSVAARLKAEAAKAEADRAAKAAAKPAPKAEPKAEAKPEAKPEAKPEAKPAEIPAKP
>NZ_CP040429.1|WP_025878304.1|396815_397508_-|rhomboid-family-intramembrane-serine-protease
MFVSLPSRKKATLRWATPVLFAALWLAFLWSISRPDDARGSLWLDWGALSTGLTHPLDWWATLQDGSVLRLFTALFLHADWSHLLGNLVFLLIFGLPAERVLGPWRLLLLFLVGGAISNLVAIYTMGSPDQIIIGASGAVSALIGAYLALFPGARLGVVIPLGLFLEFVRAPAYLLIGVWAALQVVFAYIGPTFGMVAWWAHIGGFVFGVVYGMYVRAAIARRLRKRHGF
>NZ_CP040429.1|WP_025878303.1|397734_399162_+|membrane-protein
MQTASTIARLTLLAVGVAGALAAADANAAAFQLKENSAKGLGRAFAGSTSAEGDASVVATNPASMRLLEGTQIQGDVSAISFGAKFRGEGRYANGAPISGGNGGDAGMIAPVPAAYFHVPFGEKDNMHFGVSLTVPFGFKTEYDRDWVGRYNGVKTELQAIDLGAAFSYDVNPYLSFGASVFAERLNVDLTSAVDGGTAINASAQQRAAAAALAAGRTPAQAQAAAQAAGRQAAQLGFSPGTADGYLRIKGDEVSVGYTLGMTVSPVEGTNIAFSYRSEVEHKITDGKADFTMTPAAAAFLAQAAPGTFVDSNGRATITLPASATVSFTHRVNDQWKIMADVSRTAWSKFDEVRVDYDSNQPDSVLPFHYRDTTFASIGTEYRLNEQLTLRGGLAYDQTPTTDAHRDVRVPDTTRKWLSLGLTWAPSEKMEYSVGYTHLFTKDPNINSTSATANNVVGKYKVTGDVLAASMQYKF
>NZ_CP040429.1|WP_051501537.1|399270_399711_+|hypothetical-protein
MADRRYLKKMTRYWAAEEARATVALQDALASEWFDYWHTHLDWKGRGNRHGSDRTAVAAALLRLLERAVACRRQDTQCWVVLAPDSGQSALFLHSPNPQGTPWPHPFDGVTWDIEAPDWLAPVMAPHHQLGRWGSAEPRLLVRVRA
>NZ_CP040429.1|WP_025878300.1|399782_400391_+|nicotinamide-mononucleotide-transporter
MNLSDPNFQLELAANIAVAGSILLAGRNNVHTWWLGIVGCALFAAVFERSHLYADMVLQFFFVVISVFGWWQWLRGDHGAPLPITRLPARAWSWLLPLAVLATFGYGWMLTRLTNAYAPYIDSAVLVLSVIAQILMMRRKLESWWVWLLVNTIAVPLYYSRGLHLTSILYVGFWINALVALRHWRHLMRAEADTGRAADGIA
>NZ_CP040429.1|WP_154879159.1|400377_401487_+|AAA-family-ATPase
MALPERVPRGLVVGKFCPLHLGHERLMEFASTRCTQLLVIGWSQPGFAGYSAARRERWLRARFPQATVAVLDDARLAALCRQQGVPVRALPQDKDSEQVQRAFTAWLCVALFGGPVQAVFTGEDYGDGFAAALAQHFNAPVQHHRLERSTDIGQASGTELRADPHAHRQGLSRSVYADHVQRVAFIGGESTGKSTLARVLAERQGTAWVPEFGRTLWEQQGGELQAQDLLRIAATQPQHEHQAAQHAHRWLFCDTTPLVTLGYSGWMFGTAPEPLQRAAARAYDLLFLCAPDIPFEQDGTRVGEEFRMRQHAWYLQQLQARGMAYVLLEGDLEMRIARVLEELVRRADNRFSVLAESVARGWQARIRPT
>NZ_CP040429.1|WP_154879161.1|401536_404755_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase-PutA
MNAPSSPIAASDAPRPSALLSPELPASPNPFRQAITDGWLKDEASHVRELLAQARLPADEQAKVQALAADLVARVRVRAKDQGAIEAFMRQYDLGSEEGVLLMCVAEALLRIPDQETADKLIRDKLADADWEKHLGGSDSVLVNASTWGLMLTGKLVQMNDATRADAPSAFKRLVGRVGEPVVRLAVRQAMKIMGHQFVMGRTIGEALARSHKGDSASYRYSFDMLGEGALTMKDALRYLEDYRRAIHAIGGDHKARGGRADGDVNNAPGISIKLSALYPRYEHAKRARVLKDLVPGVLELAQLAKSYGIGCTVDAEESDRLELSLDIIEQVFGDASLAGWDGFGVVVQAYQKRTPYTIDHLADMARRAGRRLQVRLVKGAYWDAEIKRAQIEGYAGYPVFTRKQNTDVSYLACAKRLFTHADAIYPMFATHNAHTIAAVRSIANGGVYEHQKLHGMGDDLYAEVVPADRLGLPCRVYAPVGSHEDLLPYLVRRLLENGANSSFVNRITDERVPIADLVRDPVEMVSSFESIPHPKIPLPVDLLRSQNHDRKNSMGANLANDNELRALAEQLNAAVKPWQAAPLVPGADPTGASLPVTNPADTREVVGQWQAADAATVQKALANAVAAQPAWNRTPAASRAAILEHAADQLEARMPEFMALCVKEAGKSLPDGIAEVREAVDFLRYYAKQAREQFSHAEKLPSPTGESNELQLHGRGVFVCISPWNFPLAIFLGQVAAALAAGNSVIAKPAEQTNLIGYYAVKLLHDAGVPADVVQYLPGDGATVGAALTADPRVAGVAFTGSTDTARAINRAMAARDAAIGVLIAETGGQNAFIADSSALPEQLVKDAIGSAFTSAGQRCSAARVLFVQDDIADKVMTMLAGAMKELKVGNPGLLSTDVGPVIDADALKILQDHAVRMDREARLIAAAELSAEAANGTFFAPRAYELKDLGKLQKEIFGPVLHVIRWKGDQLDAVIDQINATGYGLTLGVHSRIDETVDRISNGVHVGNVYVNRNQIGAVVGVQPFGGQGLSGTGPKAGGPHYLLRFATEKTVTVNTTAAGGNASLLTLGD
>NZ_CP040429.1|WP_025878297.1|405028_405505_+|DUF2244-domain-containing-protein
MIEVLTAPDGSGTQLRLRPPRALDARQFVLLFAVLSGVMWLVSAFGWVAGNAFAPLFALLYSLLLAAALRALWRSGERQEEIRVVPACVEVIPVPGGSPVFRAHPHWVRLLTDDQRVRLASSGRQVEVGSFLAPAERQTLVETLEDLLAASDGGNRRR
>NZ_CP040429.1|WP_154879162.1|405516_406473_+|cytochrome-c-oxidase-subunit-II
MKQSRGWGTKCVAMAAAMGALLSMPGTVLAQAADPKPWQLNMGKGVTQTSRLAWESNNLSLIVCTVIGVIVFGAMAYAMFKFRKSKGAVAATFSHNTKAEVIWTVIPVIILVVMAWPATANLIKMYDTRDAEMTVKVTGYQWMWKYEYLGENVTFTSRLDRESDRMRQSGKVPTRESHPHYLLDVDNRLVLPVDTKVRFVITSDDVIHAWWVPALGWKQDAIPGFINEAWTSIEQPGVYRGQCAELCGKDHGFMPIVVEAVSKEEFKQWLAQRKPAPAPAAPAAPAEPTAPASETPAQPAAPAAAEAGNAPAAAASGA

Crispr_ID: NZ_CP040429_5

• CRISPR_ID: NZ_CP040429_5
• CRISPR_location: 544122-544244
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_5

Consensus_repeat	Method
CGGCTCTGGTAGCTGCCGACCTTGGTCGGCGCTGTG	CRISPRCasFinder

spacers of NZ_CP040429_5

>5.1|544158|51|NZ_CP040429|CRISPRCasFinder
GCTGCGTGTCGACCAAGGTCGACACCTACCGGATCGGATCAGCGCTGCGCA

CRISPR arrays and Neighbor proteins around NZ_CP040429_5

CRISPR arrays

The CRISPR arrays of NZ_CP040429_5

>merge|NZ_CP040429|5|544122-544244|CRISPRCasFinder
CGGCTCTGGTAGCTGCCGACCTTGGTCGGCGCTGTGGCTGCGTGTCGACCAAGGTCGACACCTACCGGATCGGATCAGCGCTGCGCACGGCTCTGGTAGCTGCCGACCTTGGTCGGCGCTGTG

>NZ_CP040429|5|5|544122-544244|CRISPRCasFinder
CGGCTCTGGTAGCTGCCGACCTTGGTCGGCGCTGTG	GCTGCGTGTCGACCAAGGTCGACACCTACCGGATCGGATCAGCGCTGCGCA
CGGCTCTGGTAGCTGCCGACCTTGGTCGGCGCTGTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_025878403.1|536696_536972_-|DUF4031-domain-containing-protein	unknown	unknown	gnl|CDD|379076
NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein	unknown	unknown	gnl|CDD|371627
NZ_CP040429.1|WP_025878408.1|540927_541080_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_059065863.1|537628_538567_-|flagellar-motor-protein-MotB	unknown	unknown	gnl|CDD|236365
NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I	unknown	unknown	gnl|CDD|181184
NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA	unknown	unknown	gnl|CDD|179953
NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase	unknown	unknown	gnl|CDD|368316
NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase	unknown	unknown	gnl|CDD|234819
NZ_CP040429.1|WP_012509934.1|538570_539425_-|flagellar-motor-stator-protein-MotA	unknown	unknown	gnl|CDD|181655
NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV	unknown	unknown	gnl|CDD|235035
NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|183009
NZ_CP040429.1|WP_025878415.1|547716_547980_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_099782680.1|539526_539994_-|peptide-methionine-(R)-S-oxide-reductase-MsrB	unknown	unknown	gnl|CDD|234692
NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein	unknown	unknown	gnl|CDD|378666
NZ_CP040429.1|WP_154879251.1|540132_540507_+|classical-arabinogalactan-protein-4	unknown	unknown	gnl|CDD|237030
NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase	unknown	unknown	gnl|CDD|223710
NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|236842
NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase	unknown	unknown	gnl|CDD|143500
NZ_CP040429.1|WP_154879249.1|536985_537495_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase	unknown	unknown	gnl|CDD|211327

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_025878403.1|536696_536972_-|DUF4031-domain-containing-protein	gnl|CDD|379076	pfam13223, DUF4031, Protein of unknown function (DUF4031). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and viruses. Proteins in this family are typically between 91 and 130 amino acids in length. There is a conserved HYD sequence motif.	8.76064e-33
NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein	gnl|CDD|371627	pfam11607, DUF3247, Protein of unknown function (DUF3247). This family of proteins is the protein product of the gene XC5848 from Xanthomonas campestris. The protein has no known function however its structure has been determined. The protein adopts a Lsm fold however differences with the fold were observed at the N-terminal and internal regions.	2.80137e-23
NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein	gnl|CDD|378666	pfam11454, DUF3016, Protein of unknown function (DUF3016). This is a bacterial family of uncharacterized proteins.	5.63162e-64
NZ_CP040429.1|WP_059065863.1|537628_538567_-|flagellar-motor-protein-MotB	gnl|CDD|236365	PRK09041, motB, motility protein MotB.	8.11969e-163
NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I	gnl|CDD|181184	PRK07967, PRK07967, beta-ketoacyl-ACP synthase I.	0
NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA	gnl|CDD|179953	PRK05174, PRK05174, bifunctional 3-hydroxydecanoyl-ACP dehydratase/trans-2-decenoyl-ACP isomerase.	2.17929e-120
NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase	gnl|CDD|368316	pfam05175, MTS, Methyltransferase small domain. This domain is found in ribosomal RNA small subunit methyltransferase C as well as other methyltransferases.	4.77483e-66
NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase	gnl|CDD|234819	PRK00711, PRK00711, D-amino acid dehydrogenase.	0
NZ_CP040429.1|WP_012509934.1|538570_539425_-|flagellar-motor-stator-protein-MotA	gnl|CDD|181655	PRK09110, PRK09110, flagellar motor stator protein MotA.	2.39312e-164
NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV	gnl|CDD|235035	PRK02406, PRK02406, DNA polymerase IV; Validated.	0
NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator	gnl|CDD|183009	PRK11169, PRK11169, leucine-responsive transcriptional regulator Lrp.	3.14081e-70
NZ_CP040429.1|WP_099782680.1|539526_539994_-|peptide-methionine-(R)-S-oxide-reductase-MsrB	gnl|CDD|234692	PRK00222, PRK00222, peptide-methionine (R)-S-oxide reductase MsrB.	1.08674e-76
NZ_CP040429.1|WP_154879251.1|540132_540507_+|classical-arabinogalactan-protein-4	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	0.000140987
NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase	gnl|CDD|223710	COG0637, COG0637, Predicted phosphatase/phosphohexomutase [General function prediction only].	5.02579e-60
NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase	gnl|CDD|143500	cd06827, PLPDE_III_AR_proteobact, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes, Proteobacterial Alanine Racemases. This subfamily is composed mainly of proteobacterial alanine racemases (EC 5.1.1.1), fold type III PLP-dependent enzymes that catalyze the interconversion between L- and D-alanine, which is an essential component of the peptidoglycan layer of bacterial cell walls. hese proteins are similar to other bacterial ARs and are fold type III PLP-dependent enzymes containing contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Homodimer formation and the presence of the PLP cofactor are required for catalytic activity.	0
NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein	gnl|CDD|236842	PRK11091, PRK11091, aerobic respiration control sensor protein ArcB; Provisional.	3.00779e-65
NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase	gnl|CDD|211327	cd02553, PseudoU_synth_RsuA, Pseudouridine synthase, Escherichia coli RsuA like. This group is comprised of eukaryotic and bacterial proteins similar to Escherichia coli RsuA. Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil, psi). No cofactors are required. E.coli RsuA makes psi516 in 16S RNA. Psi at this position is not generally conserved in other organisms.	6.73592e-75

Protein sequences

>NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase
MRPARALIDLGALRSNYRLARELGGGKALAILKADAYGHGAVRCAQALEGEADGFGVATIEEALELRQAGIRAPILLLEGIFEPSEMALVAEHDLWFSVGSPWQLEALVAFDSPRPLTVWLKLDSGMHRLGLDVPGFRAAHARLSALPQVARIVMMTHLARADELDSERTREQAATFVEAIDGLEGETSICNSPALLGWPDVRSDWVRPGLMLYGANPLPDNSELTARLRPVMTMQSKVFAERWIEAGEPVGYGARFVAKARTRVGVVALGYADGYPQFAPNGTPVLIDGQPGGLIGRVSMDMLTVDLTAHAQAGVGSVVELWGTAPTLSELAPRCGVSAYQLPCGVKRVARVYQD
>NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase
MRVLVLGSGVIGTTSAWYLRQAGFEVTVVDRQPGPALETSFANAGQLSFGYTSPWAAPGVPKKAIGWLFEKHAPLAIKPGMDLAQYRWLWQMLRNCTHERYAINKARMVRMSEYSRDCLNELRAQIGIDFEGRDLGTTQLFRTQQQLDASAQDIEILAQYGVPYEVLDRAGIIKAEPALAHVDGLVGALRLPRDQTGDCQLFTRRLAQMAAEAGVEFRYDQDITGVESDGDRITGVRIGGKLETADRFVVALGSYSPGLVAPLGMRLPVYPLKGYSLTLPITDPAMAPTSTILDESYKVAVTRFDNRIRVGGMAEVAGFDLSLSPRRRETLELVVRDLYPKGGDLAKAEFWTGLRPATPDGTPVIGATPFRNLFLNTGHGTLGWTMACGSGRYLADLMSARQPQISTEGLDIFRYGQYRHAPQHENRTCVLPAR
>NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator
MATRPRELDKIDRKILRILQAEGRISFTELGERVGLSTTPCTERVRRLEREAVITGYHAHLDPSALKASLLVFVEISLAYKSGDIFEEFRRSALKLPNVLECHLVSGDFDYLLKARISEMASYRKLLGSTLLTLPHVRESKSYIVMEEVKETWALPIPD
>NZ_CP040429.1|WP_025878408.1|540927_541080_+|hypothetical-protein
MANQQNRHPGKEQQGKTPQEQQRQQQQQQQPNEQQKKNPQQGSMKNPQQR
>NZ_CP040429.1|WP_154879251.1|540132_540507_+|classical-arabinogalactan-protein-4
MKPCLVLLLSALLPLLAQAQVPTGSPTATRSSATVAPPPVAPPPQASRPQPQVLPSPQPAQPIRSTGPAQVTPTPAPALPDKVYDRNGRIVPGVKPVGPNRVFDSRTGRYYDSVPTGDGQQIKR
>NZ_CP040429.1|WP_099782680.1|539526_539994_-|peptide-methionine-(R)-S-oxide-reductase-MsrB
MSAFDLTPPTATQTDALVAGLSAEERRVLLQHGTEAPFCGVFLDNKREGVYCCRLCALPLFRSSTKFDSGTGWPSFFAPFDASHVREIRDTSHGMVRTEITCARCGSHLGHVFPDGPPPTYERHCLNSVSLSFTGNGEPWPDPLQRGGAEAGVAG
>NZ_CP040429.1|WP_012509934.1|538570_539425_-|flagellar-motor-stator-protein-MotA
MLIIVGFLVVIISVLGGYLGAHGRLGALWQPYELVIIGGAALGAFLVGTPAKTVKQTLQAMVGVFKGPRYKQQDYIDVLSLVYELLNKARREGFMALEDHVERPAESALFGNYPKVQADHHLIDFITDCLRLMIGSNIEPHELEPLLELELEKHHAEAMAPSQVLTKVADGLPGFGIVAAVLGIVITMGSIGGDIVEVGGHVAGALVGTFLGILLGYGFVGPMASAMEARAEQDSRIYESVKTALLACLRGYNPKIALEFARKTLPSNVRPAFSDFEQHLKTVK
>NZ_CP040429.1|WP_059065863.1|537628_538567_-|flagellar-motor-protein-MotB
MAETKPTVIVRRVKKAGHAAHHGGSWKVAYADFVTAMMAFFLVLWLMASTSKPERAAISEYFRNPSPLVGSSATPAPGMAGPGGASTSMIKLGGATDVSRGNSNDPFQNQQKSIPQPVDEQQRDKQQLEALMKELQEAISRSQALEPFKDQLLLDLTPEGLRIQIVDKQNRPMFDLGSATLKPYTQQILHELAEYLNHVPNRISLTGHTDITAYSAARGYGNWELSADRANAARRALIDGGLEDSKITRVVGLSSSVLFDKADPQNPINRRISIVVMTKAAEEAALAGAGPQVGLSATTVDPDVQAAQGSGK
>NZ_CP040429.1|WP_154879249.1|536985_537495_-|hypothetical-protein
MSKLSKAKRDKRKKQQTKRPFLRLNAQQQVQNHAVLVNEDGQAVAAIGLQGREWLLAIGGQTMGNADNPVPMLAMLKHLSNVQEAEGRKVTLEYSELMQKLLDTLAEEAGQTAEEYLGKLVAEFASEQAEDAAAEGEASDEAAADTAGAEGAADADATPAADADGKPQA
>NZ_CP040429.1|WP_025878403.1|536696_536972_-|DUF4031-domain-containing-protein
MSVYVDDAVHPWRGQRWAHLMADTLAELHAMAAQLGIPPRAFQNKASGAHYDVTAELRAQALALGAVAISRHVDRAQVKAVIANARAQYQP
>NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein
MKGSLSTALLLAGMLAVGSVAAAPRTVTAPDAPRALQADGPVSVQWNDPAKFTEIRQSTNRFEAERGDWVQQLARYVQTSAAKPLQAGQTLEVTLVDVKRAGDYEPWHGPRGRDIRIMRDIYPPRITLQYTLKDASGRIIDEGDARLSDSGYLHNIGLKSDTDPLRYEKRLIDDWVKRQLTSRVTAAR
>NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein
MMVPTPETDLHHGVLERIHAGFCVIQVLFDGDEAIDYRFLEVNDAFERHTGLKDACGKRMSTLEPHHEGDWFRIYGEVARTGRPAQFEMDARALGRTFAVDAVRVGQPGEDKVGILFFDVTARKQMEVELGESEARFSALADGLPMPVWVLDERGHARFVNSAFSEFFGGDENRVPEDVWRGLVHPDDASVFEYELQEALKAQRSMHALVRARRADGQWRWLEMNARPRFSRMGRFIGLAGSSPDVTERREIELAREELLQSERAARSAAENMARLKDEFLATLSHELRTPLTTILGWSELLLQRVDSTSPLYKGLGVIANSATAQKRLISDMLDLSSMLLGKVQLEVEVLDLRDQLNEAMGAQELVAEGKALDVTLQLPAQPCQVLGDATRLQQVFWNLLSNAIKFTPAEGRIDVQLQADGNYWTITVRDTGDGIAPEFLNHLFSRFRQADGTTTRRHGGLGLGLAIVQQLVELHGGSVSAASDGHGHGSTFTVRLPQHLPDAERRPLREVVSGPILEPMVVEPYPLRGLHVLAVEDQPEVLEYLRRMLEEQGASVSAASSAGEALALLADNGHLQYQVLLTDIGMPGMDGYGLVSTLRQDLGVDAAALPAVAVTALARADDRRRALASGFQEHVAKPYSVAQLVGVVRRVQATRGDSLLH
>NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein
MSRIAPRIHTDSAQIARLEALLPQLQGETEVQLTLHDGRRLLGTVAVQPTLQQYRNDAGDEGSNGQLRLDDLDAPVQQHHVWLDEIASIRRLPPRL
>NZ_CP040429.1|WP_025878415.1|547716_547980_-|hypothetical-protein
MRALFVGGVVDNSEMDLEGSHPPVHYPEDTGGGHSRYRLHQVGHGADGSVAYAVYGAPDLADDEVTRVAEERAYARRFEATATLFEH
>NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase
MASSDDAPLQTLFLPFSSGALRWPEGPVAFLRARDGWPLREQAGGREVDCEQSFAPFAQPLQQAAGWTVSGQLDDVAGRRGRYPLVLVLPPRQREEARALFARALALVAEGGRIVACQHNNEGARSGEGDLKQLAGLGGSLTKNHCRVFWTAPLQGQHDVDVAKRWGALDAVRPIVGGRFLSRPGVFAWDRIDPASALLAEHLPADLAGRAADLGAGYGYLSRELLERCPKITALDLYEAEKRALDLAELNLAPPPRPVPLRFLWRDVTAGIEPDYDVIISNPPFHTPSRADRPDIGQRFIAVAAQALRPGGRLYVVANRHLPYEYTLNESFGAVRVVAERDGFKLVEAVKGKGKGR
>NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase
MKLVKHIANLGYGSRKQVQWMFREGRVTDADGDVLYADDQVPHEAVRVDGEPLDPPVGLSLAMYKPAGYTCSTKDKGRLIYDLLPPRFRDRDPVLSTVGRLDRETSGLLLLTDDGNLLHRIISPKSKLPKVYEVELAEDLRGDEVALFASGTLMLEAEKTPLLPAELQVLGPRKARLVLHEGRYHQVRRMFAAAGNHVQALHRSRVGGLDLQGLAEGQWRLLTSTDLDTLFAP
>NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase
MTSIAALPFLPDAVIFDMDGLMIDSERVSLACWSEAAEEFGLPLDASFFVRMVGLGDRDSQALLRQQGIEDSMIEAMAARCHDLYEERTQTGLPLRPGILELLELLKSHAVPRAVATTTRQPRANRKLAAAGLLPYFDAVITSGDVARPKPAPDIYLLAAQRLGQAPERCLALEDSPAGTRAALAAGMTVIQVPDLVHPDEELRALGHRIVGSLVDAHALLLPLLPR
>NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I
MRRVVITGMGITSCLGNDLDTVSAALRESRAGITALADHAEAGLRSQVGGRVDLDLDALIDRKQKRFMSDAAAFAYLAMADAITDAGLTPEQVSGLRTGLIAGSGGGSSEWQVGAVDLLRSRGVRKVGPYMVPRTMCSTVSACLATAFQIKGVSYSLSAACATSAHCIGAAADLIRHGAQDIMFAGGGEDLHWSMSVMFDAMGALSTSFNDTPASASRPYDKDRDGFVIAGGGGMLVLEDYDHAVARGAHIHAELIGYGVTSDGADMVAPSGEGAVRCMKMALQNVDRPLDYLNTHGTSTPLGDVTELGAIREVFGDAIPPLSSTKALSGHSLGAASVHEAIYCLLMMRDGFVAGSANIGELDPRVEGFPILRESREQKLDTVMSNSFGFGGTNAALVFGRV
>NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA
MTRLHAFNRDQLLASARGELFGAAAGRLPNDPMLMFDRITEIREDGGPHGKGMVRAELDIRPDLWFFGCHFIGDPVMPGCLGLDAMWQLTGFFLTWLGAPGKGRALGCGEVKFTGQVLPDAKLVRYEIDISRVINRKLVMAQSDARMYVDDREIYNARDLRVGLFTETGSF
>NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV
MNALRKIIHVDMDAFYASVEQRDDPSLRGKPVVVAWRGARSVVCAASYEARVFGVRSAMPALRAERLCPDAVFVPPDFARYKAVSRHVREIFLRHTDLVEPLSLDEAYLDVTEPKSGIELATDIARTIRAQIREETNLTASAGIAPNKFLAKIASDWRKPDGQFVIPPQRVDAFLLPLPVNRVPGVGKVMEGKLAARGIVTCGDLRQWTLPDLEDAFGSFGRSLYNRARGVDERPVEPDQQVQSISSEDTFAEDLLLEDLSEAIVQLAGKTWQATRKTERIGHTVVLKLKTAQFRILTRSFTPERPPESMEELRDIALSLRARVDLPADTRYRLVGVGLGGFREKEAVVQGELFEHATNDSPRT

Crispr_ID: NZ_CP040429_6

• CRISPR_ID: NZ_CP040429_6
• CRISPR_location: 550610-550750
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_6

Consensus_repeat	Method
GGTGGGTGCCGACCGTTGGCCGGCACGCTTCACCGTTCTCGCCGGGCATGG	CRISPRCasFinder

spacers of NZ_CP040429_6

>6.1|550661|39|NZ_CP040429|CRISPRCasFinder
CCCGGCGCTACCGCCCTGGTAGGTGCCAACCTTGAACCC

CRISPR arrays and Neighbor proteins around NZ_CP040429_6

CRISPR arrays

The CRISPR arrays of NZ_CP040429_6

>merge|NZ_CP040429|6|550610-550750|CRISPRCasFinder
GGTGGGTGCCGACCGTTGGCCGGCACGCTTCACCGTTCTCGCCGGGCATGGCCCGGCGCTACCGCCCTGGTAGGTGCCAACCTTGAACCCGGTGGGTGCCGACCGTTGGTCGGCACGCTTCACCGTTCTCGCCGGGCATGG

>NZ_CP040429|6|6|550610-550750|CRISPRCasFinder
GGTGGGTGCCGACCGTTGGCCGGCACGCTTCACCGTTCTCGCCGGGCATGG	CCCGGCGCTACCGCCCTGGTAGGTGCCAACCTTGAACCC
GGTGGGTGCCGACCGTTGGTCGGCACGCTTCACCGTTCTCGCCGGGCATGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein	unknown	unknown	gnl|CDD|371627
NZ_CP040429.1|WP_154879258.1|554218_555130_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293825
NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein	unknown	unknown	gnl|CDD|378666
NZ_CP040429.1|WP_080150131.1|556974_557766_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|369777
NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA	unknown	unknown	gnl|CDD|179953
NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase	unknown	unknown	gnl|CDD|368316
NZ_CP040429.1|WP_025878427.1|558563_560405_-|TonB-dependent-vitamin-B12-receptor	unknown	unknown	gnl|CDD|273802
NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase	unknown	unknown	gnl|CDD|223710
NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|236842
NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV	unknown	unknown	gnl|CDD|235035
NZ_CP040429.1|WP_025878426.1|557816_558485_+|phosphoglycolate-phosphatase	unknown	unknown	gnl|CDD|319854
NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|183009
NZ_CP040429.1|WP_025878415.1|547716_547980_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025878428.1|560919_561498_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_CP040429.1|WP_154879260.1|555303_555942_-|NAD(P)H-binding-protein	unknown	unknown	gnl|CDD|225462
NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I	unknown	unknown	gnl|CDD|181184
NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase	unknown	unknown	gnl|CDD|234819
NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase	unknown	unknown	gnl|CDD|143500
NZ_CP040429.1|WP_025878424.1|556048_556978_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176114
NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase	unknown	unknown	gnl|CDD|211327

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein	gnl|CDD|371627	pfam11607, DUF3247, Protein of unknown function (DUF3247). This family of proteins is the protein product of the gene XC5848 from Xanthomonas campestris. The protein has no known function however its structure has been determined. The protein adopts a Lsm fold however differences with the fold were observed at the N-terminal and internal regions.	2.80137e-23
NZ_CP040429.1|WP_154879258.1|554218_555130_-|MBL-fold-metallo-hydrolase	gnl|CDD|293825	cd07739, metallo-hydrolase-like_MBL-fold, uncharacterized subgroup of the MBL-fold_metallo-hydrolase superfamily; MBL-fold metallo hydrolase domain. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	8.38761e-97
NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein	gnl|CDD|378666	pfam11454, DUF3016, Protein of unknown function (DUF3016). This is a bacterial family of uncharacterized proteins.	5.63162e-64
NZ_CP040429.1|WP_080150131.1|556974_557766_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	1.66577e-15
NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA	gnl|CDD|179953	PRK05174, PRK05174, bifunctional 3-hydroxydecanoyl-ACP dehydratase/trans-2-decenoyl-ACP isomerase.	2.17929e-120
NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase	gnl|CDD|368316	pfam05175, MTS, Methyltransferase small domain. This domain is found in ribosomal RNA small subunit methyltransferase C as well as other methyltransferases.	4.77483e-66
NZ_CP040429.1|WP_025878427.1|558563_560405_-|TonB-dependent-vitamin-B12-receptor	gnl|CDD|273802	TIGR01779, Vitamin_B12_transporter_BtuB, TonB-dependent vitamin B12 receptor. This model represents the TonB-dependent outer membrane receptor found in gamma proteobacteria responsible for translocating the cobalt-containing vitamin B12 (cobalamin). [Transport and binding proteins, Other, Transport and binding proteins, Porins].	0
NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase	gnl|CDD|223710	COG0637, COG0637, Predicted phosphatase/phosphohexomutase [General function prediction only].	5.02579e-60
NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein	gnl|CDD|236842	PRK11091, PRK11091, aerobic respiration control sensor protein ArcB; Provisional.	3.00779e-65
NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV	gnl|CDD|235035	PRK02406, PRK02406, DNA polymerase IV; Validated.	0
NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator	gnl|CDD|183009	PRK11169, PRK11169, leucine-responsive transcriptional regulator Lrp.	3.14081e-70
NZ_CP040429.1|WP_025878426.1|557816_558485_+|phosphoglycolate-phosphatase	gnl|CDD|319854	cd16417, HAD_PGPase, Escherichia coli Gph phosphoglycolate phosphatase and related proteins; belongs to the haloacid dehalogenase-like superfamily. Phosphoglycolate phosphatase (PGP; EC 3.1.3.18) catalyzes the conversion of 2-phosphoglycolate into glycolate and phosphate. Members of this family belong to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase (C-Cl bond hydrolysis), azetidine hydrolase (C-N bond hydrolysis); phosphonoacetaldehyde hydrolase (C-P bond hydrolysis), phosphoserine phosphatase and phosphomannomutase (CO-P bond hydrolysis), P-type ATPases (PO-P bond hydrolysis) and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	3.28506e-81
NZ_CP040429.1|WP_025878428.1|560919_561498_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	4.30623e-32
NZ_CP040429.1|WP_154879260.1|555303_555942_-|NAD(P)H-binding-protein	gnl|CDD|225462	COG2910, COG2910, Putative NADH-flavin reductase [General function prediction only].	1.95014e-67
NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I	gnl|CDD|181184	PRK07967, PRK07967, beta-ketoacyl-ACP synthase I.	0
NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase	gnl|CDD|234819	PRK00711, PRK00711, D-amino acid dehydrogenase.	0
NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase	gnl|CDD|143500	cd06827, PLPDE_III_AR_proteobact, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes, Proteobacterial Alanine Racemases. This subfamily is composed mainly of proteobacterial alanine racemases (EC 5.1.1.1), fold type III PLP-dependent enzymes that catalyze the interconversion between L- and D-alanine, which is an essential component of the peptidoglycan layer of bacterial cell walls. hese proteins are similar to other bacterial ARs and are fold type III PLP-dependent enzymes containing contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Homodimer formation and the presence of the PLP cofactor are required for catalytic activity.	0
NZ_CP040429.1|WP_025878424.1|556048_556978_+|LysR-family-transcriptional-regulator	gnl|CDD|176114	cd08422, PBP2_CrgA_like, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA and its related homologs, contains the type 2 periplasmic binding domain. This CD includes the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA and its related homologs. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.76834e-81
NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase	gnl|CDD|211327	cd02553, PseudoU_synth_RsuA, Pseudouridine synthase, Escherichia coli RsuA like. This group is comprised of eukaryotic and bacterial proteins similar to Escherichia coli RsuA. Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil, psi). No cofactors are required. E.coli RsuA makes psi516 in 16S RNA. Psi at this position is not generally conserved in other organisms.	6.73592e-75

Protein sequences

>NZ_CP040429.1|WP_033830258.1|549904_550588_+|HAD-family-phosphatase
MTSIAALPFLPDAVIFDMDGLMIDSERVSLACWSEAAEEFGLPLDASFFVRMVGLGDRDSQALLRQQGIEDSMIEAMAARCHDLYEERTQTGLPLRPGILELLELLKSHAVPRAVATTTRQPRANRKLAAAGLLPYFDAVITSGDVARPKPAPDIYLLAAQRLGQAPERCLALEDSPAGTRAALAAGMTVIQVPDLVHPDEELRALGHRIVGSLVDAHALLLPLLPR
>NZ_CP040429.1|WP_154879256.1|549206_549908_+|pseudouridine-synthase
MKLVKHIANLGYGSRKQVQWMFREGRVTDADGDVLYADDQVPHEAVRVDGEPLDPPVGLSLAMYKPAGYTCSTKDKGRLIYDLLPPRFRDRDPVLSTVGRLDRETSGLLLLTDDGNLLHRIISPKSKLPKVYEVELAEDLRGDEVALFASGTLMLEAEKTPLLPAELQVLGPRKARLVLHEGRYHQVRRMFAAAGNHVQALHRSRVGGLDLQGLAEGQWRLLTSTDLDTLFAP
>NZ_CP040429.1|WP_154879254.1|548136_549210_+|methyltransferase
MASSDDAPLQTLFLPFSSGALRWPEGPVAFLRARDGWPLREQAGGREVDCEQSFAPFAQPLQQAAGWTVSGQLDDVAGRRGRYPLVLVLPPRQREEARALFARALALVAEGGRIVACQHNNEGARSGEGDLKQLAGLGGSLTKNHCRVFWTAPLQGQHDVDVAKRWGALDAVRPIVGGRFLSRPGVFAWDRIDPASALLAEHLPADLAGRAADLGAGYGYLSRELLERCPKITALDLYEAEKRALDLAELNLAPPPRPVPLRFLWRDVTAGIEPDYDVIISNPPFHTPSRADRPDIGQRFIAVAAQALRPGGRLYVVANRHLPYEYTLNESFGAVRVVAERDGFKLVEAVKGKGKGR
>NZ_CP040429.1|WP_025878415.1|547716_547980_-|hypothetical-protein
MRALFVGGVVDNSEMDLEGSHPPVHYPEDTGGGHSRYRLHQVGHGADGSVAYAVYGAPDLADDEVTRVAEERAYARRFEATATLFEH
>NZ_CP040429.1|WP_025878414.1|547175_547466_+|DUF3247-family-protein
MSRIAPRIHTDSAQIARLEALLPQLQGETEVQLTLHDGRRLLGTVAVQPTLQQYRNDAGDEGSNGQLRLDDLDAPVQQHHVWLDEIASIRRLPPRL
>NZ_CP040429.1|WP_025878413.1|545142_547131_+|PAS-domain-S-box-protein
MMVPTPETDLHHGVLERIHAGFCVIQVLFDGDEAIDYRFLEVNDAFERHTGLKDACGKRMSTLEPHHEGDWFRIYGEVARTGRPAQFEMDARALGRTFAVDAVRVGQPGEDKVGILFFDVTARKQMEVELGESEARFSALADGLPMPVWVLDERGHARFVNSAFSEFFGGDENRVPEDVWRGLVHPDDASVFEYELQEALKAQRSMHALVRARRADGQWRWLEMNARPRFSRMGRFIGLAGSSPDVTERREIELAREELLQSERAARSAAENMARLKDEFLATLSHELRTPLTTILGWSELLLQRVDSTSPLYKGLGVIANSATAQKRLISDMLDLSSMLLGKVQLEVEVLDLRDQLNEAMGAQELVAEGKALDVTLQLPAQPCQVLGDATRLQQVFWNLLSNAIKFTPAEGRIDVQLQADGNYWTITVRDTGDGIAPEFLNHLFSRFRQADGTTTRRHGGLGLGLAIVQQLVELHGGSVSAASDGHGHGSTFTVRLPQHLPDAERRPLREVVSGPILEPMVVEPYPLRGLHVLAVEDQPEVLEYLRRMLEEQGASVSAASSAGEALALLADNGHLQYQVLLTDIGMPGMDGYGLVSTLRQDLGVDAAALPAVAVTALARADDRRRALASGFQEHVAKPYSVAQLVGVVRRVQATRGDSLLH
>NZ_CP040429.1|WP_025878412.1|544329_544896_-|DUF3016-domain-containing-protein
MKGSLSTALLLAGMLAVGSVAAAPRTVTAPDAPRALQADGPVSVQWNDPAKFTEIRQSTNRFEAERGDWVQQLARYVQTSAAKPLQAGQTLEVTLVDVKRAGDYEPWHGPRGRDIRIMRDIYPPRITLQYTLKDASGRIIDEGDARLSDSGYLHNIGLKSDTDPLRYEKRLIDDWVKRQLTSRVTAAR
>NZ_CP040429.1|WP_025878411.1|543049_544120_+|alanine-racemase
MRPARALIDLGALRSNYRLARELGGGKALAILKADAYGHGAVRCAQALEGEADGFGVATIEEALELRQAGIRAPILLLEGIFEPSEMALVAEHDLWFSVGSPWQLEALVAFDSPRPLTVWLKLDSGMHRLGLDVPGFRAAHARLSALPQVARIVMMTHLARADELDSERTREQAATFVEAIDGLEGETSICNSPALLGWPDVRSDWVRPGLMLYGANPLPDNSELTARLRPVMTMQSKVFAERWIEAGEPVGYGARFVAKARTRVGVVALGYADGYPQFAPNGTPVLIDGQPGGLIGRVSMDMLTVDLTAHAQAGVGSVVELWGTAPTLSELAPRCGVSAYQLPCGVKRVARVYQD
>NZ_CP040429.1|WP_032976409.1|541766_543071_+|D-amino-acid-dehydrogenase
MRVLVLGSGVIGTTSAWYLRQAGFEVTVVDRQPGPALETSFANAGQLSFGYTSPWAAPGVPKKAIGWLFEKHAPLAIKPGMDLAQYRWLWQMLRNCTHERYAINKARMVRMSEYSRDCLNELRAQIGIDFEGRDLGTTQLFRTQQQLDASAQDIEILAQYGVPYEVLDRAGIIKAEPALAHVDGLVGALRLPRDQTGDCQLFTRRLAQMAAEAGVEFRYDQDITGVESDGDRITGVRIGGKLETADRFVVALGSYSPGLVAPLGMRLPVYPLKGYSLTLPITDPAMAPTSTILDESYKVAVTRFDNRIRVGGMAEVAGFDLSLSPRRRETLELVVRDLYPKGGDLAKAEFWTGLRPATPDGTPVIGATPFRNLFLNTGHGTLGWTMACGSGRYLADLMSARQPQISTEGLDIFRYGQYRHAPQHENRTCVLPAR
>NZ_CP040429.1|WP_025878409.1|541137_541617_-|AsnC-family-transcriptional-regulator
MATRPRELDKIDRKILRILQAEGRISFTELGERVGLSTTPCTERVRRLEREAVITGYHAHLDPSALKASLLVFVEISLAYKSGDIFEEFRRSALKLPNVLECHLVSGDFDYLLKARISEMASYRKLLGSTLLTLPHVRESKSYIVMEEVKETWALPIPD
>NZ_CP040429.1|WP_025878419.1|550801_552010_-|beta-ketoacyl-ACP-synthase-I
MRRVVITGMGITSCLGNDLDTVSAALRESRAGITALADHAEAGLRSQVGGRVDLDLDALIDRKQKRFMSDAAAFAYLAMADAITDAGLTPEQVSGLRTGLIAGSGGGSSEWQVGAVDLLRSRGVRKVGPYMVPRTMCSTVSACLATAFQIKGVSYSLSAACATSAHCIGAAADLIRHGAQDIMFAGGGEDLHWSMSVMFDAMGALSTSFNDTPASASRPYDKDRDGFVIAGGGGMLVLEDYDHAVARGAHIHAELIGYGVTSDGADMVAPSGEGAVRCMKMALQNVDRPLDYLNTHGTSTPLGDVTELGAIREVFGDAIPPLSSTKALSGHSLGAASVHEAIYCLLMMRDGFVAGSANIGELDPRVEGFPILRESREQKLDTVMSNSFGFGGTNAALVFGRV
>NZ_CP040429.1|WP_025878420.1|552009_552525_-|3-hydroxyacyl-[acyl-carrier-protein]-dehydratase-FabA
MTRLHAFNRDQLLASARGELFGAAAGRLPNDPMLMFDRITEIREDGGPHGKGMVRAELDIRPDLWFFGCHFIGDPVMPGCLGLDAMWQLTGFFLTWLGAPGKGRALGCGEVKFTGQVLPDAKLVRYEIDISRVINRKLVMAQSDARMYVDDREIYNARDLRVGLFTETGSF
>NZ_CP040429.1|WP_025878421.1|552716_553811_+|DNA-polymerase-IV
MNALRKIIHVDMDAFYASVEQRDDPSLRGKPVVVAWRGARSVVCAASYEARVFGVRSAMPALRAERLCPDAVFVPPDFARYKAVSRHVREIFLRHTDLVEPLSLDEAYLDVTEPKSGIELATDIARTIRAQIREETNLTASAGIAPNKFLAKIASDWRKPDGQFVIPPQRVDAFLLPLPVNRVPGVGKVMEGKLAARGIVTCGDLRQWTLPDLEDAFGSFGRSLYNRARGVDERPVEPDQQVQSISSEDTFAEDLLLEDLSEAIVQLAGKTWQATRKTERIGHTVVLKLKTAQFRILTRSFTPERPPESMEELRDIALSLRARVDLPADTRYRLVGVGLGGFREKEAVVQGELFEHATNDSPRT
>NZ_CP040429.1|WP_154879258.1|554218_555130_-|MBL-fold-metallo-hydrolase
MRTAALLLPLALAASFTSAPLLAAPAAPAPASAAKSQLRLQTFHPGPQAMFSVSSVLIEGRNDAILVNAQFAAGDARRLVEQIRASGKRLTTIYISHGDPDYYFGLATVQDAFPQARIVATAQTVAHIRESQAGKLAYWGPKMGADAPARIVVPAVLEGDALQLEGRRLPLIGLDGPTPDRSVLWVPSLRAIVGGIPVVAGEHVWMADTQTPQSHADWLRTLQQLQALKPKVVVPGHYAEGAVLDASALRFTADYIRAFDVETAKAKDSAALVKAMQARYPQLAGVASLELSAKVAKGEMQWP
>NZ_CP040429.1|WP_154879260.1|555303_555942_-|NAD(P)H-binding-protein
MKIALVGATGNIGRQIARHALANGHQLTVIVRSAQDLPAELAGAHPVIASLDDQDALVAAITGHDVLASAYGPRPGDDIGRVGEVAAQLANAARKANVPRLVVVGGAGSLEVAPGVQLVDTPTFPDAYKPYALAHREAFNRLQAVDDLDWTFFSPAAEIGPGEERGQYRVQPKAFLADASGHSRISYADYGAAFVAELEAHKHPRQIITAAY
>NZ_CP040429.1|WP_025878424.1|556048_556978_+|LysR-family-transcriptional-regulator
MDRLTAMTVFVEVAERGSLTAAAEVLDMSRAMVSRYLAEVEGWLGARLLHRTTRRVSLTGAGEAALARFRQMLAIGEELQGELASDDPEPHGTLRITASVSFGQSHLARAVAAFVQRHPAARIELLLVDRMVNLVEERVDLAVRIARQIDPSLIARRLAICRSVLCATPAYLQARGTPTAPEHLAVHNCLTHHYVGKSLWQLHREGRSLSVAVGGNISANEASLLLEAVRANAGIAMLPTYQVAPLLRSGELIELLPEYSLDELGIHAVYASRRQQPVIMRRFLDFLAECFASPAFQDLDWRPSGKENT
>NZ_CP040429.1|WP_080150131.1|556974_557766_+|class-I-SAM-dependent-methyltransferase
MNHGQALIDHNRAAWDRQASEVREWSRPVDAETIAAAREGRWQVHLTPRALPLDWLGDVRGRRILCLASAGGQQAPVLAAAGAEVTVFDLSDGQLAQDRAVADRDGLSLRTVQGDMRDLQAFASDSFDVVFHPISNLYVPDVRPVWAECRRVLARDGLLMASFYNPVVFVAARDAQLSEQGLIRPQYAIPYSDLEDLEPAAREAKLARGEALTFGHSLGDLIAGQLDAGFVIDRFMEDWQPQPRFLIDRYLPTFLATRARRIG
>NZ_CP040429.1|WP_025878426.1|557816_558485_+|phosphoglycolate-phosphatase
MSYPYPLVVFDLDGTLVDSAADIAEALNRTLEDIGLARVPEATVLGWIGDGVRRLVEQAVQAAGRQIDLAAVMPTFMVHYRECLLRSPQLFAGVVDALAQLRALNVPLAICTNKPAALVPPLLQHLGIADAFALVLGGDSLPQRKPSGEPLRHIAAHFELPVDACLMVGDSLTDYRAAEDAGMPIALVRYGYPRGLDLENAQAVAVIDDLRELPGLAAVSAI
>NZ_CP040429.1|WP_025878427.1|558563_560405_-|TonB-dependent-vitamin-B12-receptor
MKLQSRMLSLAVLAALPALALADDGAADLDQVLVTATRTPIALQDSIAPAQVIDRAQIESSQATSLQELLQGRAGINLTNAGGLGKQSSLFLRGTNSSHTVVLVDGVRINSADLGLAMYQDLPLAQIERVEIVRGPQSSLYGADAIGGVIQIFTRRNQGDFAPHFQLGGGSNGLREASGGIGGGTERGWFGADIAYQHSDGIDACRGSATLFTGCFADEPDRDGYRNLSKSLRGGYNLSDQWTVEGSALRADGKNHYDGYYNYSETRQQVLAGKVRYTPSEQLTLTANVGRSDNESDNFGDFGARGSAQTHRDSASLQADIGIAEGQLLSAGVDWSEDNLDGSSAGYLVDSRRNTGVFLQYQARFGRHQLQASARNDDNQQFGNHATGSLGWAMELGHGLRVNASYGTAFKAPTFSDLYDPWSGVPTLDPEKSKSANLGISQQGQGWRWGLDVYETRIDDLITYDAATFRMQQVEKARIRGAELTGGATVAGFDINAQLSFTDPRNRTNGSAQFDNWLARRAQQTARLDIDRRFGDFRTGLTVQGAGKRYDDAANAVKVGGYGTLDLRAEYALTPAWSVLARVANVFDREYETVAWFNQPGREYQLSVRYQPR
>NZ_CP040429.1|WP_025878428.1|560919_561498_+|histidine-phosphatase-family-protein
MILDLVRHAGNGRDEFLDGRSDPPQLARLPQELVDAYAGQSWERVISSPRLRSLHTAMALATPRALDVEADEEWEELDFGDWDGQSLFDLPEEALAAFHADPHAFPPPHGESWGHFERRIARALDRLLDDDDPPPTVVVSHGGPLRMVLSLVCGLPMSLCWALRIDHGTRLRVWVERGEVGLVGELLELQQP

Crispr_ID: NZ_CP040429_7

• CRISPR_ID: NZ_CP040429_7
• CRISPR_location: 1042632-1042739
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_7

Consensus_repeat	Method
GTGGGTGCCGACCGTTGGTCGGCACGGA	CRISPRCasFinder

spacers of NZ_CP040429_7

>7.1|1042660|52|NZ_CP040429|CRISPRCasFinder
TGCCCCCATGGCCGTTCATCCAAGCATGGCGTGGATCTACTGGAGATGGCGG

CRISPR arrays and Neighbor proteins around NZ_CP040429_7

CRISPR arrays

The CRISPR arrays of NZ_CP040429_7

>merge|NZ_CP040429|7|1042632-1042739|CRISPRCasFinder
GTGGGTGCCGACCGTTGGTCGGCACGGATGCCCCCATGGCCGTTCATCCAAGCATGGCGTGGATCTACTGGAGATGGCGGGTGGGTGCCGACCGTTGCTCGGCACGGA

>NZ_CP040429|7|7|1042632-1042739|CRISPRCasFinder
GTGGGTGCCGACCGTTGGTCGGCACGGA	TGCCCCCATGGCCGTTCATCCAAGCATGGCGTGGATCTACTGGAGATGGCGG
GTGGGTGCCGACCGTTGCTCGGCACGGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_025874076.1|1039885_1041148_+|beta-ketoacyl-ACP-synthase-II	unknown	unknown	gnl|CDD|235987
NZ_CP040429.1|WP_140228414.1|1044533_1045490_+|DNA-polymerase-III-subunit-delta'	unknown	unknown	gnl|CDD|181551
NZ_CP040429.1|WP_154879505.1|1048149_1050288_+|TonB-dependent-siderophore-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP040429.1|WP_099783014.1|1041240_1042605_+|aminodeoxychorismate-synthase-component-I	unknown	unknown	gnl|CDD|236371
NZ_CP040429.1|WP_025874062.1|1051966_1053247_+|ricin-type-beta-trefoil-lectin-domain-protein	unknown	unknown	gnl|CDD|366226
NZ_CP040429.1|WP_025879386.1|1035291_1035486_+|50S-ribosomal-protein-L32	unknown	unknown	gnl|CDD|234901
NZ_CP040429.1|WP_025874077.1|1039500_1039740_+|acyl-carrier-protein	unknown	unknown	gnl|CDD|179197
NZ_CP040429.1|WP_025874071.1|1045486_1045840_+|pilus-assembly-protein-PilZ	unknown	unknown	gnl|CDD|225756
NZ_CP040429.1|WP_025879388.1|1036628_1037411_+|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|226168
NZ_CP040429.1|WP_025874078.1|1038604_1039348_+|3-oxoacyl-ACP-reductase-FabG	unknown	unknown	gnl|CDD|187594
NZ_CP040429.1|WP_154879507.1|1050299_1051805_+|PepSY-domain-containing-protein	unknown	unknown	gnl|CDD|377164
NZ_CP040429.1|WP_154879501.1|1033987_1034560_-|septum-formation-inhibitor-Maf	unknown	unknown	gnl|CDD|234855
NZ_CP040429.1|WP_132825782.1|1047069_1047450_+|tautomerase-family-protein	unknown	unknown	gnl|CDD|379645
NZ_CP040429.1|WP_025879387.1|1035577_1036555_+|ketoacyl-ACP-synthase-III	unknown	unknown	gnl|CDD|236475
NZ_CP040429.1|WP_025874079.1|1037577_1038522_+|ACP-S-malonyltransferase	unknown	unknown	gnl|CDD|223408
NZ_CP040429.1|WP_025879385.1|1034674_1035184_+|characterized-ACR-protein	unknown	unknown	gnl|CDD|236878
NZ_CP040429.1|WP_154879503.1|1046083_1046512_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_099842022.1|1047641_1048031_+|DUF2946-domain-containing-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_099841998.1|1042813_1043875_+|endolytic-transglycosylase-MltG	unknown	unknown	gnl|CDD|224475
NZ_CP040429.1|WP_059063248.1|1043871_1044537_+|dTMP-kinase	unknown	unknown	gnl|CDD|234814

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_025874076.1|1039885_1041148_+|beta-ketoacyl-ACP-synthase-II	gnl|CDD|235987	PRK07314, PRK07314, beta-ketoacyl-ACP synthase II.	0
NZ_CP040429.1|WP_140228414.1|1044533_1045490_+|DNA-polymerase-III-subunit-delta'	gnl|CDD|181551	PRK08769, PRK08769, DNA polymerase III subunit delta'; Validated.	0
NZ_CP040429.1|WP_154879505.1|1048149_1050288_+|TonB-dependent-siderophore-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	9.78245e-76
NZ_CP040429.1|WP_099783014.1|1041240_1042605_+|aminodeoxychorismate-synthase-component-I	gnl|CDD|236371	PRK09070, PRK09070, aminodeoxychorismate synthase component I.	0
NZ_CP040429.1|WP_025874062.1|1051966_1053247_+|ricin-type-beta-trefoil-lectin-domain-protein	gnl|CDD|366226	pfam00652, Ricin_B_lectin, Ricin-type beta-trefoil lectin domain.	1.28278e-23
NZ_CP040429.1|WP_025879386.1|1035291_1035486_+|50S-ribosomal-protein-L32	gnl|CDD|234901	PRK01110, rpmF, 50S ribosomal protein L32; Validated.	4.13245e-21
NZ_CP040429.1|WP_025874077.1|1039500_1039740_+|acyl-carrier-protein	gnl|CDD|179197	PRK00982, acpP, acyl carrier protein; Provisional.	7.11963e-35
NZ_CP040429.1|WP_025874071.1|1045486_1045840_+|pilus-assembly-protein-PilZ	gnl|CDD|225756	COG3215, PilZ, Tfp pilus assembly protein PilZ [Cell motility and secretion / Intracellular trafficking and secretion].	3.05824e-60
NZ_CP040429.1|WP_025879388.1|1036628_1037411_+|serine/threonine-protein-phosphatase	gnl|CDD|226168	COG3642, COG3642, Mn2+-dependent serine/threonine protein kinase [Signal transduction mechanisms].	0.00413549
NZ_CP040429.1|WP_025874078.1|1038604_1039348_+|3-oxoacyl-ACP-reductase-FabG	gnl|CDD|187594	cd05333, BKR_SDR_c, beta-Keto acyl carrier protein reductase (BKR), involved in Type II FAS, classical (c) SDRs. This subgroup includes the Escherichai coli K12 BKR, FabG. BKR catalyzes the NADPH-dependent reduction of ACP in the first reductive step of de novo fatty acid synthesis (FAS). FAS consists of four elongation steps, which are repeated to extend the fatty acid chain through the addition of two-carbo units from malonyl acyl-carrier protein (ACP): condensation, reduction, dehydration, and a final reduction. Type II FAS, typical of plants and many bacteria, maintains these activities on discrete polypeptides, while type I FAS utilizes one or two multifunctional polypeptides. BKR resembles enoyl reductase, which catalyzes the second reduction step in FAS. SDRs are a functionally diverse family of oxidoreductases that have a single domain with structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet) NAD(P)(H) binding region and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H) binding pattern: TGxxxGxG in classical SDRs. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P) binding motif and an altered active site motif (YXXXN). Fungal type type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P) binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr-151 and Lys-155, and well as Asn-111 (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	1.3404e-123
NZ_CP040429.1|WP_154879507.1|1050299_1051805_+|PepSY-domain-containing-protein	gnl|CDD|377164	pfam03929, PepSY_TM, PepSY-associated TM region. The PepSY_TM family is so named because it is an alignment of up to five transmembranes helices found in bacterial species some of which carry a nested PepSY domain, pfam03413.	0.000744997
NZ_CP040429.1|WP_154879501.1|1033987_1034560_-|septum-formation-inhibitor-Maf	gnl|CDD|234855	PRK00884, PRK00884, Maf-like protein; Reviewed.	5.95218e-97
NZ_CP040429.1|WP_132825782.1|1047069_1047450_+|tautomerase-family-protein	gnl|CDD|379645	pfam14552, Tautomerase_2, Tautomerase enzyme.	1.11675e-41
NZ_CP040429.1|WP_025879387.1|1035577_1036555_+|ketoacyl-ACP-synthase-III	gnl|CDD|236475	PRK09352, PRK09352, beta-ketoacyl-ACP synthase 3.	0
NZ_CP040429.1|WP_025874079.1|1037577_1038522_+|ACP-S-malonyltransferase	gnl|CDD|223408	COG0331, FabD, (acyl-carrier-protein) S-malonyltransferase [Lipid metabolism].	4.19098e-124
NZ_CP040429.1|WP_025879385.1|1034674_1035184_+|characterized-ACR-protein	gnl|CDD|236878	PRK11193, PRK11193, 23S rRNA accumulation protein YceD.	5.56434e-30
NZ_CP040429.1|WP_099841998.1|1042813_1043875_+|endolytic-transglycosylase-MltG	gnl|CDD|224475	COG1559, COG1559, Aminodeoxychorismate lyase [Coenzyme transport and metabolism].	5.75967e-138
NZ_CP040429.1|WP_059063248.1|1043871_1044537_+|dTMP-kinase	gnl|CDD|234814	PRK00698, tmk, thymidylate kinase; Validated.	1.5998e-90

Protein sequences

>NZ_CP040429.1|WP_099783014.1|1041240_1042605_+|aminodeoxychorismate-synthase-component-I
MTHAPLIHPLPHPIDLLALQQRDPARFPLLMESTASGTAQGRWSLLLAAQGDTLQLDADGQVRDQHGAVQPGSFLQALDRAWQAQRLPHDGGHALPFRGGWALMLDYEVASQVEPVLPARARDDGRPTALALRCPAAVLHDHQADASFLIAEAGEQALLDSLVALVAGELPPAGQGWQPPQSVSEDEPQRFTEGVRRVIDYLRAGDVFQVNLSRRWSAHFAAPVSPQALYAQLRRANPAPFAGLFSAHGRHVVSSSPERLVSVHGGHAQTRPIAGTRPRFEGDDDAARIQELVGHPKERAEHVMLIDLERNDLGRICLPGTVVVDELMTVESYAHVHHIVSNVSGQLRADVTPGEVIAATFPGGTITGCPKVRCMQIISELEQVPRGAYTGAFGWLNRDGDLDLNILIRTAEVDGNEVSFRTGAGIVVDSDPDKELDETRAKARGLLRALGQQG
>NZ_CP040429.1|WP_025874076.1|1039885_1041148_+|beta-ketoacyl-ACP-synthase-II
MKRRVVVTGLGMVSPLGNDLASSWEGITHGRSGIGPLTNVSDAYLERFTTKIAGEVKGFDITADNELFGKYRVSGKDAKKMDPFIHYGLGAAFMALHDSGLEITDANADRIGAIVGAGIGGLLGIEEQTIEFHEGKKISPFYVPKTIINMLPGQLSIISGLKGPSFSAVSACATSNHSIGTAMRMIQYGDADVMVAGGAERGSSPTALGGFCAMKAMSTRNDAPEQASRPWDKDRDGFVLGDGAGILILEEYEHAKARGAKIYCELAGFGASSDAYHMTAPSENGEGAARCMTMAMKDAGVTPEQVGYLNAHGTSTPLGDLGETMAMKTAFGDHAYKMMVSSTKSMTGHLLGAAGGVEAIFSVLAMRDNVIPPTINLQQPGEGCDLDYVPNEARQAKVDVVMSNGFGFGGTNGTLIFKRV
>NZ_CP040429.1|WP_025874077.1|1039500_1039740_+|acyl-carrier-protein
MSTIEERVKKIVIEQLGVKEEEVTNSASFVDDLGADSLDTVELVMALEEEFECEIPDEEAEKISTVQAAITYITAHVKA
>NZ_CP040429.1|WP_025874078.1|1038604_1039348_+|3-oxoacyl-ACP-reductase-FabG
MSKPLQGEIALVTGASRGIGAAIADLLAAQGATVIGTATTDSGAAAIGERLAAHGGHGRALNVTDAAALDAVLDGIAKEFGPISILVNNAGITRDNLLMRMKEDDWASIIDTNLTSVFRTSKAVMRGMMKARKGRIINIASVVGVTGNAGQANYAAAKAGIIGFSKSLAKEIGSRGVTVNVVAPGFIDTDMTKALPEEARTALIGDIALERLGSPEDIAHAVAFLASPAAGYITGETLHVNGGMYMP
>NZ_CP040429.1|WP_025874079.1|1037577_1038522_+|ACP-S-malonyltransferase
MTVSTLAFVFPGQGSQSVGMLAELAELHPQVREAFTEASDGAGVDLWALSQGGPEEMLNRTEYTQPALLAASIGAWRAWNAVGGPRPSVLAGHSLGEYTALVAAGALSLHDGAHLVRLRGQLMQDAAPAGVGAMAAVLGAEDQLVLDVCAEAAGSQVVVPANFNSPGQIVIGGDAAAVDRALALLAEKGVRKAVKLAVSVPSHTPLMREAANRLAEVMAGLSWQLPQLPVVQNVDAKVHDGVDAIRAALVQQLYQPVQWTGCVQALAARGVTRIAECGPGKVLTGLVKRIDKAIDGRSLATPGDFETARETWSA
>NZ_CP040429.1|WP_025879388.1|1036628_1037411_+|serine/threonine-protein-phosphatase
MVEPIVIEGQRAWLKQYGEGSRAVALGLLNFVARRFHLDALRPPPHRGGDAARETEARRLAELQAQGVNVPAVIGSGHAALVIGDNGSSFNTCLREADDAGRDRLVTAAMQAIAEAHARGAYFGQPLPRNLTWDGQNVGFIDFEEDPLEVMDLAEAQARDWLMFGYGVAKYYADRPESLQAMMAEAMNGVQAPVRAHVHAVSGRLQRLARVCMKLGRSARALAHSIFITHGATTLGLLMVVGLCMDWFADGELDILQLLC
>NZ_CP040429.1|WP_025879387.1|1035577_1036555_+|ketoacyl-ACP-synthase-III
MSKRIYSRIAGTGSYLPEKVLTNADLEKMVETSDEWIQTRTGIRERHIAAEGETTSDLGYQAALRAIEAAGIDASQLDMIVVGTTTPDLIFPSTACLIQAKLGVSGCPAFDVNAACSGFVFALSVADKFIRSGDARHVLVIGTETLTRIVDWEDRTTCVLFGDGAGAVVLKADEETGILSTHLHSDGSKKELLWNPVGVSVGFGEGNNGGGTINMKGNDVFKYAVKALDSVVDETLDANGLTKSDLDWLIPHQANLRIIEATAKRLEMSMDQVVVTVDKHGNTSSASVPLALDAAVRSGRVERGQLLLLEAFGGGFTWGSALLRY
>NZ_CP040429.1|WP_025879386.1|1035291_1035486_+|50S-ribosomal-protein-L32
MAVQKSRVTPSRRGQRRSHDALSAKQLSTDPTTGEVHLRHHITADGFYRGKKVIQTKSSAVQED
>NZ_CP040429.1|WP_025879385.1|1034674_1035184_+|characterized-ACR-protein
MSANVPETLDAWRMVVARRRFDGQVPLAELTRLQGLVADTEGECNYSLEFGRDEILRVSYVELTIDTALPLTCQRSMQRFLLPVKMTQRLGLIREEDEESSLPEEYEPLLVPEDGQLRPLDLVEDELVLAVPVVPLSPYGEAVDKDWAPTEEEIEKANPFAALAALKKQ
>NZ_CP040429.1|WP_154879501.1|1033987_1034560_-|septum-formation-inhibitor-Maf
MPALVLASTSRYRRDLLERLGLPFDCARPQVDETAEADEAPLALAARLASAKAAEVAARHPGSWVIGSDQVADLNGQPLGKPGTVEAACAQLAAMSGQTVRFHTAVSLIRDGESLSAMDTTQVRFRALQAPEIARYVAIEQPLDCAGSFKCEGLGISLFEAIDNRDPTALIGLPLIALCGLLRRAGFAVP
>NZ_CP040429.1|WP_099841998.1|1042813_1043875_+|endolytic-transglycosylase-MltG
MAGAKRGCLLVVTLLLVLAAIVAGAGAWFFYKQSQFADVPLTPSADSVVIASGDGMNSVLRKLREAGVDEGQDTQWQLLARQLDAAGKLKVGEYALSKDLTPRELLLRMRAGKVLQHRVTIIEGWNIRQLRAALKRADPLLHTTDTLDDAALMDRLGFAGQHPEGRFLPETYVYQRGDSDLDVLKRAHGAMEKALDEAWESRAPDLPINTPYELLTLASIIEKETALASERPQIAGVFMRRLKIGMRLQTDPTVIYGIGAAYDGNIRRRDLTTDTPYNTYTRSGLTPTPIAMPSRDALMAAAQPAPGDALYFVAVGDGSGAHVFSPSLDKHNAAVARYLQQLRQQRTQETPAQ
>NZ_CP040429.1|WP_059063248.1|1043871_1044537_+|dTMP-kinase
MSSALLRHPRFVSLEGGEGAGKTTAINAIRECLRRHGHEVVLTREPGGTPLAERIRGLVLKPDAEIAAEPLSAEAELLLVFAARAQHVRQVIQPALQRGAYVLSDRFTDSSYAYQGGGRGLDPQWIADLERRAVGLLPGLTLLLDVDVAVGRARANSRDLWPDRIESEQDDFFQRVREVFRSRAQQDPQRFALVDAGQVQERVAADVVARVERWLQQGEGA
>NZ_CP040429.1|WP_140228414.1|1044533_1045490_+|DNA-polymerase-III-subunit-delta'
MSTFSPWQQRAFDQTVAALDADRLGHGLLICGPAGLGKREVALALADHVLARGDATHATRTRQLIAAGTHPDLQLISFIPNKSGDKLRTEIVIEQVREITNKLALTPQYGVAQVVIVDPADAINRSAANALLKTLEEPQPGRYLWLISSDPARLPQTVRSRCQRLEFKLPPREEALAWLQQQGHSEAAAHEALDAARGHPGQADNWLREDGLSLRREVGRELEQLAAGKTGAVELAQKWCADDNAALRLRFAADLALAQASTDALTTPERLHKLAAWFDAANRTRDLLRTTVRADLAVVELLLAWNKVNERPAARGNR
>NZ_CP040429.1|WP_025874071.1|1045486_1045840_+|pilus-assembly-protein-PilZ
MSASNARQGILSLAVKDKAALYSAYMPFVKNGGIFVPTPKRYFLGDEVFLLLTLPDSSERLPVAGKVIWVTPAGAQGNRTAGIGVQLADGQEGETVRHKIETILAGLTGSDKPTHTM
>NZ_CP040429.1|WP_154879503.1|1046083_1046512_-|hypothetical-protein
MTNNTVLIPRLHALIGEMASNVPEDLAREIECALKEQQFPPAQPMFFTFLDAIRRGEGEDGQPCTTQMLNAQTLASLGRSLSALTAVLDLLHAAERARVDGNTDEQIGDFHRNGLLLAARQIAHAAQTGLGDAITAVANKPG
>NZ_CP040429.1|WP_132825782.1|1047069_1047450_+|tautomerase-family-protein
MPLARIDLRKGKSVEYRQRVGEAIYQAMRAVGVPENDRFQIFQEHDAGTLVYDPGYLGIARTDDFICIQITWNEGRTLEQKKALYAGIADGLHAAVGIRREDVFINLVEVKRENWSFGNGQAQYVS
>NZ_CP040429.1|WP_099842022.1|1047641_1048031_+|DUF2946-domain-containing-protein
MLLVLFAPLVSRWLVHGHVVASAAPVAAMDHAAHTQHAMEGHHDHHAMAMQHGEATPKPPADPHADHEMGVDCDYCLIAARLITLLVAALLLMILLAPVCRALRGSVQTLPQRICGTLGARGPPVLLAV
>NZ_CP040429.1|WP_154879505.1|1048149_1050288_+|TonB-dependent-siderophore-receptor
MKTTPNFAPLRWAMLPALCASFLQATPALAADAVLPTTLDTVRVVDTRSGSLSSTANTGSALGLSVLQTPASLTVISREQLEQRGDSNLNDAITRAGAISAMPHPGNGLSALSSRGFTDGASVMRLYDGLRQYGGVGITFPFDTWSIERIEVLRGPASVIHGDGAIGGVVNIVPKKPSRGAIENEVSVTLGSEDTARLGFGSGGALTPALAYRVDVSGNYSSGWVDRGQNGDATFSAALLWQPRTDLQFTLTHAQGYQKPMRYFGTPLIDGRQLGALRHENYNVADSVIRFRDRWIQLDALWSPNENVEWRTRVYQIDSQRDWRNAEAYVYNGRTGLIDRSGNTQITHNQDQTGLTSTLRLLGNAGGLPNSFAVGFDANRAHFKHTNNTYAGSSGPVDPFNPVPGGFSSDAPNLPRYRNSAEQVALFVEDRLELSERWSVLAGLRHDRATIDRNDLVSGQRAFSRTYNSTGWRAGTVFALQPTLTLYAQYSQAADPVSGLLMISPANGAFDLAKGKQIEVGMKQAFDGGEWTLAAYRIRKTGLLSRDPLQPDRRVQVGAQTSKGIEASLNWNFAPQWSLDANATVLKAGFEDFLEATGTPVVIVSRDGNVPPNVAERLANVWLSWQFQPDWSVASGVRYVGKRYADNANTLQLPGYATTDLALTWQAAPRTRLTARMFNVFDKAYYATAYYTSTQWLLGADRRVEFSLDHRF
>NZ_CP040429.1|WP_154879507.1|1050299_1051805_+|PepSY-domain-containing-protein
MSLRSTAKRWTYLTHRWLGIGGCLLMLLWFVSGMVMLFVGYPKLTPAERLAALPALVDARGWQALSVLPEVVRQAPERVVLTTLRGEPAYVVRSGANVGAWSVLTGQALPPVSAQLAEVSAAQFAGGPAFVGAMPLDEDRWTHSRALDPHRPLYRVGVGGAQPGDVYVSSRTGEVVLDAPRLQQRWNYVGAWLHWLYFLRMQSVDPVWTWTVIVLSALCTVAAISGVVVGIWRWRFRGQYRSGSKTPYQEPWMRWHHLIGLMASAFVFTWIFSGLMSMNPLGVFSSTGVVIDTAHYRGGVVTGEGALAEPGRLLAASTDVGFVPVEIQWRRIGGELFAVLLDGQGDTRIVSAVEGRLRVARLLPEAWLKQKVQAMSAAPIQGFTIRQAPDAYFYARAPEAMNGAAVRRFPVAVAWFGDAEATRVYIDLATGDPLLTMGHRERAGRWLFSFLHSWDLPAALRQQNTRLGVLLLLSVAGTALCTTAAVIGYRRLRMKVRRRRP
>NZ_CP040429.1|WP_025874062.1|1051966_1053247_+|ricin-type-beta-trefoil-lectin-domain-protein
MNYVSMGVLAIGIAAASSSVQAKSLPRLYSFPTTTTASVSNALPAPGQVIQLSAQVDGQALGLYHIPGNEQIGGFVEFKVNGQAVGKVQVSTVNTPFLGTVSDLDKGCWDAIRDVQACTHKYAYGRPARVAINYTVPAGFTTASITATFSGDGQFTQGSVSAPVNLRNIPTFGEIRGMGNKCLDAEGANTAPGTAIQVWDCTPGTAQQLWTVKPNTSTITGVPSNRVLDIVGYGTSNGSRIQLYDAHGDWNQSWKFTNTSIVGVANKVLDAIGASSANGTKIQLYSNALTSNQKWEFNPANGSIVGVGGKCLDVEGANSADGTRVQLWDCTGVPQQRFELGADGSIRGLGGKCLEAADGASHDGNPIRMWSCNGGAHQSWRLVGEIRNPQTNMCLDDPGMGNANGSKVHMWMCQGTENQRWEFSSY

Crispr_ID: NZ_CP040429_8

• CRISPR_ID: NZ_CP040429_8
• CRISPR_location: 1758489-1758560
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_8

Consensus_repeat	Method
GTAGATCCACGCCATGCGTGGAT	CRISPRCasFinder

spacers of NZ_CP040429_8

>8.1|1758512|26|NZ_CP040429|CRISPRCasFinder
ATCGCGGAAAAGATCGGATGGACAAC

CRISPR arrays and Neighbor proteins around NZ_CP040429_8

CRISPR arrays

The CRISPR arrays of NZ_CP040429_8

>merge|NZ_CP040429|8|1758489-1758560|CRISPRCasFinder
GTAGATCCACGCCATGCGTGGATATCGCGGAAAAGATCGGATGGACAACGTAGATCCACGCCATGCGTGGAT

>NZ_CP040429|8|8|1758489-1758560|CRISPRCasFinder
GTAGATCCACGCCATGCGTGGAT	ATCGCGGAAAAGATCGGATGGACAAC
GTAGATCCACGCCATGCGTGGAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_025879447.1|1759249_1759756_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_033830819.1|1750747_1751443_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|378924
NZ_CP040429.1|WP_025879444.1|1761808_1762369_-|glycine-cleavage-system-protein-R	unknown	unknown	gnl|CDD|225337
NZ_CP040429.1|WP_025878934.1|1745812_1746739_-|c-type-cytochrome	unknown	unknown	gnl|CDD|225797
NZ_CP040429.1|WP_154881325.1|1746735_1748082_-|c-type-cytochrome	unknown	unknown	gnl|CDD|365823
NZ_CP040429.1|WP_025879443.1|1762533_1763427_+|4-hydroxy-tetrahydrodipicolinate-synthase	unknown	unknown	gnl|CDD|235107
NZ_CP040429.1|WP_025878941.1|1754692_1755613_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176122
NZ_CP040429.1|WP_154879987.1|1756518_1757445_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|227099
NZ_CP040429.1|WP_154879982.1|1748265_1749417_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|366166
NZ_CP040429.1|WP_032976527.1|1749420_1750560_-|MFS-transporter	unknown	unknown	gnl|CDD|340951
NZ_CP040429.1|WP_025879445.1|1761237_1761717_-|peroxiredoxin	unknown	unknown	gnl|CDD|224146
NZ_CP040429.1|WP_025878940.1|1753850_1754552_-|pirin-family-protein	unknown	unknown	gnl|CDD|380375
NZ_CP040429.1|WP_154879990.1|1757441_1758251_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	unknown	unknown	gnl|CDD|180561
NZ_CP040429.1|WP_154879985.1|1751600_1753796_+|TonB-dependent-siderophore-receptor	unknown	unknown	gnl|CDD|227114
NZ_CP040429.1|WP_088101377.1|1763459_1763975_+|hypothetical-protein	unknown	unknown	gnl|CDD|225854
NZ_CP040429.1|WP_033830828.1|1766843_1768223_+|polynucleotide-adenylyltransferase-PcnB	unknown	unknown	gnl|CDD|236939
NZ_CP040429.1|WP_059063786.1|1758570_1759239_-|DUF1275-domain-containing-protein	unknown	unknown	gnl|CDD|377734
NZ_CP040429.1|WP_059063791.1|1764848_1766273_+|sugar-porter-family-MFS-transporter	unknown	unknown	gnl|CDD|340917
NZ_CP040429.1|WP_005409054.1|1764338_1764662_-|ferredoxin-family-protein	unknown	unknown	gnl|CDD|378771
NZ_CP040429.1|WP_025879446.1|1759752_1761153_-|PhoH-family-protein	unknown	unknown	gnl|CDD|224787

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_033830819.1|1750747_1751443_+|alpha/beta-hydrolase	gnl|CDD|378924	pfam12697, Abhydrolase_6, Alpha/beta hydrolase family. This family contains alpha/beta hydrolase enzymes of diverse specificity.	1.14341e-15
NZ_CP040429.1|WP_025879444.1|1761808_1762369_-|glycine-cleavage-system-protein-R	gnl|CDD|225337	COG2716, GcvR, Glycine cleavage system regulatory protein [Amino acid transport and metabolism].	8.2524e-74
NZ_CP040429.1|WP_025878934.1|1745812_1746739_-|c-type-cytochrome	gnl|CDD|225797	COG3258, COG3258, Cytochrome c [Energy production and conversion].	1.38571e-76
NZ_CP040429.1|WP_154881325.1|1746735_1748082_-|c-type-cytochrome	gnl|CDD|365823	pfam00034, Cytochrom_C, Cytochrome c. The Pfam entry does not include all Prosite members. The cytochrome 556 and cytochrome c' families are not included. All these are now in a new clan together. The C-terminus of DUF989, pfam06181, has now been merged into this family.	1.25691e-09
NZ_CP040429.1|WP_025879443.1|1762533_1763427_+|4-hydroxy-tetrahydrodipicolinate-synthase	gnl|CDD|235107	PRK03170, PRK03170, dihydrodipicolinate synthase; Provisional.	3.66137e-130
NZ_CP040429.1|WP_025878941.1|1754692_1755613_+|LysR-family-transcriptional-regulator	gnl|CDD|176122	cd08431, PBP2_HupR, The C-terminal substrate binding domain of LysR-type transcriptional regulator, HupR, which regulates expression of the heme uptake receptor HupA; contains the type 2 periplasmic binding fold. HupR, a member of the LysR family, activates hupA transcription under low-iron conditions in the presence of hemin. The expression of many iron-uptake genes, such as hupA, is regulated at the transcriptional level by iron and an iron-binding repressor protein called Fur (ferric uptake regulation). Under iron-abundant conditions with heme, the active Fur repressor protein represses transcription of the iron-uptake gene hupA, and prevents transcriptional activation via HupR. Under low-iron conditions with heme, the Fur repressor is inactive and transcription of the hupA is allowed. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	4.67826e-67
NZ_CP040429.1|WP_154879987.1|1756518_1757445_-|alpha/beta-fold-hydrolase	gnl|CDD|227099	COG4757, COG4757, Predicted alpha/beta hydrolase [General function prediction only].	6.7892e-13
NZ_CP040429.1|WP_154879982.1|1748265_1749417_+|alpha/beta-fold-hydrolase	gnl|CDD|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	4.26717e-14
NZ_CP040429.1|WP_032976527.1|1749420_1750560_-|MFS-transporter	gnl|CDD|340951	cd17393, MFS_MosC_like, Membrane protein MosC and similar proteins of the Major Facilitator Superfamily of transporters. The gene encoding Sinorhizobium meliloti membrane protein MosC is part of the mos locus, which encodes the biosynthesis of the rhizopine 3-O-methyl-scyllo-inosamine. MosC belongs to the bacterial fucose permease, eukaryotic Major facilitator superfamily domain-containing protein 4 (FucP/MFSD4) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.27221e-82
NZ_CP040429.1|WP_025879445.1|1761237_1761717_-|peroxiredoxin	gnl|CDD|224146	COG1225, Bcp, Peroxiredoxin [Posttranslational modification, protein turnover, chaperones].	1.97433e-70
NZ_CP040429.1|WP_025878940.1|1753850_1754552_-|pirin-family-protein	gnl|CDD|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.88467e-74
NZ_CP040429.1|WP_154879990.1|1757441_1758251_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	gnl|CDD|180561	PRK06427, PRK06427, bifunctional hydroxy-methylpyrimidine kinase/ hydroxy-phosphomethylpyrimidine kinase; Reviewed.	1.76288e-129
NZ_CP040429.1|WP_154879985.1|1751600_1753796_+|TonB-dependent-siderophore-receptor	gnl|CDD|227114	COG4773, FhuE, Outer membrane receptor for ferric coprogen and ferric-rhodotorulic acid [Inorganic ion transport and metabolism].	0
NZ_CP040429.1|WP_088101377.1|1763459_1763975_+|hypothetical-protein	gnl|CDD|225854	COG3317, NlpB, Uncharacterized lipoprotein [Cell envelope biogenesis, outer membrane].	0.00415078
NZ_CP040429.1|WP_033830828.1|1766843_1768223_+|polynucleotide-adenylyltransferase-PcnB	gnl|CDD|236939	PRK11623, pcnB, poly(A) polymerase I; Provisional.	6.29228e-172
NZ_CP040429.1|WP_059063786.1|1758570_1759239_-|DUF1275-domain-containing-protein	gnl|CDD|377734	pfam06912, DUF1275, Protein of unknown function (DUF1275). This family consists of several hypothetical bacterial proteins of around 200 residues in length. The function of this family is unknown although most members have 6 TM regions, and may be putative permeases.	1.22262e-35
NZ_CP040429.1|WP_059063791.1|1764848_1766273_+|sugar-porter-family-MFS-transporter	gnl|CDD|340917	cd17359, MFS_XylE_like, D-xylose-proton symporter and similar transporters of the Major Facilitator Superfamily. This subfamily includes bacterial transporters such as D-xylose-proton symporter (XylE or XylT), arabinose-proton symporter (AraE), galactose-proton symporter (GalP), major myo-inositol transporter IolT, glucose transport protein, putative metabolite transport proteins YfiG, YncC, and YwtG, and similar proteins. The symporters XylE, AraE, and GalP facilitate the uptake of D-xylose, arabinose, and galactose, respectively, across the boundary membrane with the concomitant transport of protons into the cell. IolT is involved in polyol metabolism and myo-inositol degradation into acetyl-CoA. The XylE-like subfamily belongs to the Glucose transporter -like (GLUT-like) family of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.24182e-154
NZ_CP040429.1|WP_005409054.1|1764338_1764662_-|ferredoxin-family-protein	gnl|CDD|378771	pfam11953, DUF3470, Domain of unknown function (DUF3470). This presumed domain is functionally uncharacterized. This domain is found in bacteria. This domain is about 50 amino acids in length. This domain is found associated with pfam00037. This domain has a single completely conserved residue N that may be functionally important.	7.04517e-20
NZ_CP040429.1|WP_025879446.1|1759752_1761153_-|PhoH-family-protein	gnl|CDD|224787	COG1875, COG1875, NYN ribonuclease and ATPase of PhoH family domains [General function prediction only].	0

Protein sequences

>NZ_CP040429.1|WP_154879990.1|1757441_1758251_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase
MSPTTPVSALTIAGSDSGGGAGIQADLKAFAAHRVHGLSVIAALTAQNTRGVRAVHVPPIDFLRAQIEACFDDFDIHAVKLGMLANAEVIHAVADALERHRPPHVVLDPVMVATSGARLLEDGALQAMRQRLLPLATLVTPNAPEAELLVGRSIANGNDAERAAASLLDLGAGAVLLKGGHLHEGNRVVDRYFDGVSSEEFIHARLPLDAHGTGCTLASAIAAQLCNGLSLANACEAGIDYVARGLQQGYAPGRSEVLVLDHFGAAPHA
>NZ_CP040429.1|WP_154879987.1|1756518_1757445_-|alpha/beta-fold-hydrolase
MSDSPRALTVNSGDGHRFDVIACVPAQPLARLLWLPALGVAARHYVPLAQALAARGVAVYLHEWRGNGSSSLRPSRSQDWGYRQILDHDLPASQALLADADDAQEVLPWIIGGHSLGGQLACVHAGRQPQAFDRLWLAASGTPFWRTFPPPRGWLLPLIYRFLPWIARRQGVLHGRRLGFGGTEARGLIADWARVGLSNHYAAAGMDEDLDAQMARVHGSAQAVLMEDDWLAPSGSMQALLAKLPNVASELRVLSAQELGTQADHFAWMKHPEAVAEAFFIQLGENFHKSVDDSRRHPHNSAPVAGRP
>NZ_CP040429.1|WP_025878941.1|1754692_1755613_+|LysR-family-transcriptional-regulator
MLKLSLDALQILDAIDRRGSFAGAGKALHKVPSTISYTVAKLEEDLGVQLFDRIGPRAEPTEAGRALLEEGRHLLRAARELELRVRRVASGWEAELTLAVDSVFPTWLLGPDIAAFREVAAPTRLRLFGEALSGTWEALLDRRADLLVAAPGEGPSGGGYVVEPLGSVDFVFAVAPGHPLASVPGVLGREQLAPYCAIAVSDSARRLLPRTVGLLMGQETLTVPDMASKLKLQCQGLGFGFLPEPCARAAVARGQLVIREVEEHKPEETFWLAWRTGEDGAALRWWRERLRRPELLAQWWQAMAEG
>NZ_CP040429.1|WP_025878940.1|1753850_1754552_-|pirin-family-protein
MLQIRKSATRGLAEHGWLSSRHTFSFASYYDPRYVSFGPLRVINEDKVIGGQGFGTHSHSNMEIVSYVLGGALEHKDSMGTGSVLRYGDVQRMSAGSGVSHSEFNHSASDPVHFLQIWIFPEAENIAPSYEETHFTPESKRGQLRLIASPDGADGSLHIHQDARIFATILDGEQKLHHALAAGRGAYVQVARGQLQVNGITLEAGDALQVSDEAQLTLENGNDAEVLVFDLKL
>NZ_CP040429.1|WP_154879985.1|1751600_1753796_+|TonB-dependent-siderophore-receptor
MSSVPVRFSVLSLRRRPLANALAQGLLLTTVATAGAASAQSAPVEEEGRTASQTLQTVQVTANQLGTITEGSGAYTPGTIATATRLVLTPRQTPQTISVITRAQMDDFGLDGIDDVMRVTPGISIVTYDSERTEYYARGFAVQNFQYDGIPMSRDSAYSAGNTLSDTAIYDRIEVLKGATGLLTGMGDPGATINLVRKKPGKEFAGSATLGVGRWDDYRAEVDVGGPLTADGRVRGRAVGAWQDKHSNLDFYQRTSKVGYAVLEADLGERTLLTVGGDVLESDPKGSTWGGIPLLDSQGNFNDMPRSFNNGTHWSGWRQYVRTGFATLEHTFDNDWVAKLQLNHQVNGYDAALAGAAGGNPDPVTGEGVSLWLGKYVGKTVSNAADFYLSGNFGLFGRQHELVVGGSASRKRWTNTGYSPQPGYPTAVADYNSWKGDIPEPEWQRGYGNNEVTRENGLYVVGRFDVADPLKVIVGSRLASYRSPQTRETGVFVPYAGVVYDLGQHYSVYASYSTIFKPHSERDEQGKALDPLEGRSYEMGLKAEFLDGRFNASAALFQLDQDNFAQPTGGKTPNGEDAYRALMGVRTKGYELEMSGQLAEGWQVQGGFAHKIARQAGSKVTTLEPENQFSLHTSYRLRGDWQGLTVGGGARWQDSTFGDITNPASGTSVVHRTQPYWLLDAMARYQFNDRLSATVNVNNLLDKRYYTIFSWYSTYTWGEPRNVRLAVTYRF
>NZ_CP040429.1|WP_033830819.1|1750747_1751443_+|alpha/beta-hydrolase
MSTTPTILLVHGFWGGAAHWGKVILELHRKGHDQVKAVELPLTSLVNDAERTRRMIRQIDGPVVLVGHSYGGAVITEAGNQPNVQALVYIAAFAPDSGESPGGITQQHLPEAAPNLAPDSDGYLWLRADKFHESFCQDLSADEGWVMAVTQKAPLASTFGDAISDPAWKHKPSWYQLSSQDRMIAPQNQKAMAERMQPKRLLQLEASHASLASHPSEVAALILEAVAAVDG
>NZ_CP040429.1|WP_032976527.1|1749420_1750560_-|MFS-transporter
MTPSSPRAQQHATRAAFFIPGFATAAWAPMVPFAKAKAGLSDASLGGLLLCLGLGSLLAMPLAGALTARLGSRRLMIATTALILLALPLLTLAPTPLALGATLFVFGAGVGAMDCTMNMQAVAVERDAGRPMMSGFHAFYSIGGFIGAGCMTGLLVLGTPLWLASLVAVAAMLLVALLSAPHWRPQRILHDGPMLALPHGVVLFISVLAFVVFLAEGSMLDWSAVFLAEIRHVPRDQAGAGFAVFTLAMTAMRLFGDGIVERLGRTRTIVIGGITAAAGFALATLVPSFAMALVGYVLVGLGCANIVPALFSMAGQQRAMPESIAITAVTTLGYAGILAGPAAIGALAHATSLGFAFLCVAAMLLGVAASARSLARRLP
>NZ_CP040429.1|WP_154879982.1|1748265_1749417_+|alpha/beta-fold-hydrolase
MKRLLLLLLACAGLWLAACSSSMTASSTSLSDRLIAPGGVSTLLDQPRIAAAVAALPNRHGFAPGRDGVPIFWRAFDPGDYGARYHYLPQQHQNGLPLDTGLSLSVPQPFRAQAPRGTVVLLHGWMMNGDSMLPWSLQLAESGYRVITLDLRNHGQSGAGPSGYGTYESDDVVDVIAELRARGEVTGPLYLFGVSYGAATALFTADKLGDQVAGVVAMESFANAGVAIRTMIPHLMALQPEGLKAQAIASYARWRYGSQDINQVVAAASRRIDVDLDKVDVTRALADTRACVLLLHGQGDQHIPVSQGRALAQANPRAHYIEMRGEDHITLPLRLDLLAGVVDDWMARDEHHPKAACPAPQLPAQAEWLVHGVDTPAKTPARG
>NZ_CP040429.1|WP_154881325.1|1746735_1748082_-|c-type-cytochrome
MRTPFKLAIALAATLAAAYGIARSTPYWFAPPQHAEVDIHDPALIEQGRYLSRAADCAACHTAPGGRPFAGGLGMQTPMGTLYSTNITPDTETGIGAYDYADFERAVRRGIRHDGQPLYPAMPYASYVIASDAEIKALYAYFMGAVQPVRQDNADSTIPWPANMRWPLAWWQLLFARPRSFSPDPTLDAGQQRGAELVEGLAHCGACHTPRGLAFQEKAMADDGSRQFLSGSVLEGWYAKNLRNEQTGLASWSEAEIVEFLRTGRTDRSAAFGGMADVVEHSTQYLSDADLLAMARYLKQLPAREGRSAQWTPGTDTTTAALRGGDYRVAGSLAYAEHCQACHRADGRGMPRVYPALAGNSIVFADDPSSLVQVTLTGGRTPHTAHDRMAFTMPGFEQLPNAQLADILTFIRNSWGNQASAVTELDVARMRRVVRDKPAHVVPQETAQ
>NZ_CP040429.1|WP_025878934.1|1745812_1746739_-|c-type-cytochrome
MRRSKKRSTALIASAVVAVLLAGAGTLLYQHLYPDLDAEVARTLDILDSHGQVVGQYHVPSAEEIASLGNADAVMFGRRLLNETARLLPDNVGNDLNCNSCHMAEGKRPFGNHYLNTGGGSYPRYMPRPGREIGLAERINGCLQRSMNGKPLAKDAPEMRAMLEYMAWLSRPVPEGARVAAPSEGPIDSTLTPDPIRGQALYAAQCAACHGDNGEGRRDASGDIAFPPLWGERSFNIGAGMARLYKAAGFVKHNMPPATTREPPLGQQVMPDQDAVDIASYFINQPRPDFAGKAKDWPRDPKPKDARY
>NZ_CP040429.1|WP_059063786.1|1758570_1759239_-|DUF1275-domain-containing-protein
MGIRLPTWVWIGAVALSCVAGMVNVVGFLGFEHQAVSHMTGSTSQLGMALAQGDWRAVGHLWGLLIAFSLGAMVSGLLIQDSALQLGRRYGVALALESLLLLAAIPLFKQHQIWGALAAAMACGLQNAMATTFSGAVVRTTHLSGMFTDLGIGLGHLLRGLPLQVRRLTLSGLIISGFLAGGVIGAWLFVRWQYDALLAPALLTGLTGLGYVSYQQWARWRR
>NZ_CP040429.1|WP_025879447.1|1759249_1759756_-|hypothetical-protein
MNRCTRLLLPSLAVAIATLLGACATTQGPASVPTTERSGQSWVVTRPIIAAQVLDTCSRPSPGREAGRVSGYWAPSRQQVDQLEAKLASLEAQVPHVLDFDRQYVGIELDGKQVIYINAFHLPEDNSLRPAREAVRVCDGGAQFWGAVFDPASGTFSELQFNGGFGGP
>NZ_CP040429.1|WP_025879446.1|1759752_1761153_-|PhoH-family-protein
MTRGKRIYVLDTNVLMHDPTALFKFEEHDVYLPMQVIEELDNGKKGTTEASRNARQVSRFLNELVQASGLDNLAEGIPLQRPQGLQLRGKQSVGLLRFQTSHFDAGKSFGKVIPDNAILGAILALKEETPEIPVVFVSKDINLRIKAAIAGIVSEDYENDRALDDFSLLYTGATELPEDFWKRHGEDLRSWSDKGRTHYEILAQDGEEWYPNQYVYLPGEDEVELRVSRIVGDGKVVLSLVDDFRHGSHAVWGISARNREQNFALNALMDPEIDFVTLLGTAGTGKTLLALAAGLAQTMDQQRYREIIMTRATVSVGEDIGFLPGTEEEKMTPWMGALTDNLEVLTHNQEGGTWGRQATNDLLASRIKIRSMNFMRGRTFLSRYLILDEAQNLTPKQMKTLITRAGPGTKIVCLGNVEQIDTPYLTETTSGLTYAVDRFKNWPHSAHITLRRGERSRLADYASEVL
>NZ_CP040429.1|WP_025879445.1|1761237_1761717_-|peroxiredoxin
MNNGDTLDSTTLSLPLALSGGAQATLGDYAGQWLVLYFYPKDSTPGCTTEGIDFNALLPDFQKAGAVVLGVSRDSVKSHDNFCAKQGFAFPLVSDADEALCSAFDVIKMKNMYGKQVRGIERSTFLISPDSRIVQSWRKVKVAGHADAVLAELKANQSK
>NZ_CP040429.1|WP_025879444.1|1761808_1762369_-|glycine-cleavage-system-protein-R
MTDTTPRPAPSENHLLINAYTTHPESPLLSVTRRIADSGCNLVDARLATVGRDVSVTALATGSWDSVAKLEAMLTRLEREEGLKLVWYRTEAKQAQSNLLPYIVEVIAADKPGILFQLADFFDRQGITIETLQSTRYRAMQTGAEMFSAQVTIGVPANMHIAALRDDFLEFCDHLNLDAIMDPMKF
>NZ_CP040429.1|WP_025879443.1|1762533_1763427_+|4-hydroxy-tetrahydrodipicolinate-synthase
MSLSGLITALATPFRADGALDPDGWQRLLHLQLEGGVQGVVVAGSTGEAATLSDAEYDQLLASAVERIAGRVPVLAGTGLSGTAKTIEQTRRAAALGATHALVVTPPYVRPTQAGLIAHYRAVADQAGVPVVLYNVPGRTGCDMLPETVAELASHPNIVGIKEAVGDTGRVRALLDLRSPTFAVLTGDDGTAARSIQAGMDGLISVGSNVLPGAYRRMCDLAAARDHEAVESWDARLQPFHDFCGVESNPIPVKALLRRIGIGHDLRLPLLPLSAAHAPAADHLAGDIAALEALSSH
>NZ_CP040429.1|WP_088101377.1|1763459_1763975_+|hypothetical-protein
MRQSVSAVRVLSFALLAVATAAGTTGCFKRGVKGDYALAPEVRPLEVPPDLNLPAGAGNNQVPTLSSATKPATPAAAAPAVSATGFTITGSKDEAFAKVGTALEGVEGLTIATRAQLLGSYDVAYEGSNFLVRVVAVDAGAYISAVDPRGLPATAEAPVKLIAALKAKLAP
>NZ_CP040429.1|WP_005409054.1|1764338_1764662_-|ferredoxin-family-protein
MPFVVTENCIKCKHTDCVEVCPVDCFHEGPNFLVIDPDECIDCTLCEPECPVNAIFPEDDVPAGQEGFVALNAELAKEWPVLTVRKDPPADAGEWDGKPDKLKLLER
>NZ_CP040429.1|WP_059063791.1|1764848_1766273_+|sugar-porter-family-MFS-transporter
MSPVQPGAASNGGENTAFIVLISCAATLGGFLFGFDSGVINGTVDGLRQAFNSSEAALGFEVASMLLGCAIGAFVAGWLGDRLGRRGVLIVAAVMFLVSALGAGAAHASWLFVCARVLGGFAVGAASVMSPAYIAEVASARYRGRLATVQQMAIICGLFAAFLSNYLLARAAGASTEPLWLGQEAWRWMFWMQALPSLLFLLLLLVIPESPRFLVMKGRQAQARAVLGRLYGERAAVNKQAEIEASLSQDQHKPRFGDLINKATGKLRPIVWVGIGLAMFQQLVGINVVFYYGAVLWQAVGFSESDALLINVLSGALSIGACLLTVVLIDRIGRKPLLWVGSVGMSVALVLMVVAFASGSLAEGRLQLSDGMGRLALVAANVYVVFFNMSWGPVMWVMLGEMFPNQIRGPALAVAGAAQWTSNFAITVTFPMLLAGIGLAGAYGIYTVAAILSIIFVIRYVRETKGKELEQMEG
>NZ_CP040429.1|WP_033830828.1|1766843_1768223_+|polynucleotide-adenylyltransferase-PcnB
MGNPETSTGSANIISSATSPFSLRVIPRDQHTISRKDISPNALRVLYRLRDAGFGAYLVGGAVRDLLVNGQPKDFDVATDATPEQVKQLFRNCRLIGRRFRLAHVVFGREIIEVATFRANIDDGSGDREMENGMLVRDNVYGSIEDDAIRRDFTCNALYYAIEDFSVRDYTGGFEDVQARLMKLIGDPVQRYQEDPVRMLRAVRLAAKLGFQIEEGTAAPIPQLAGLLNEAAPARLFEEVLKLFLSGHGVASFEGLERYGLFDVLFPESAKALKSNRTGALRRMLVEGLANTDARVANDEPVSPAFLFALLLWPAYCRAQATLLKQGVAPEEAQRRAADRVTVQQLSTIALPRRFSLPMQEIWLLQARFSSRQRKRVMRTLSHPRFRAAFDFLALRQVASAEHEADVAFWREAQAQSGHELDSSLDSLHSDAGDEEGGAPRKRRRRRRRPDGAAAGAAE

Crispr_ID: NZ_CP040429_9

• CRISPR_ID: NZ_CP040429_9
• CRISPR_location: 2127669-2127848
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP040429_9

Consensus_repeat	Method
GAGCCCGGTAGGTGTCGACCTTGGTCGACAC	PILER-CR

spacers of NZ_CP040429_9

>9.1|2127700|37|NZ_CP040429|PILER-CR
AGCAGATCCAGACCATGCGTGGATGCCTCCCAATGCC
>9.2|2127768|70|NZ_CP040429|PILER-CR
AGCGCCAACCAAGGTTGGCGGCTACCAGGGCGGTCGATCGAGGTTGACCGGCTGCGGCAGGCGTTCCTGG

CRISPR arrays and Neighbor proteins around NZ_CP040429_9

CRISPR arrays

The CRISPR arrays of NZ_CP040429_9

>merge|NZ_CP040429|9|2127669-2127848|PILER-CR
GAGCCCGGTAGGTGTCGACCTTGGTCGACACAGCAGATCCAGACCATGCGTGGATGCCTCCCAATGCCCCGCGCGGTAGAGCGCCAACCAAGGTTGGCGGCTACCAGGGCGGTCGATCGAGGTTGACCGGCTGCGGCAGGCGTTCCTGGGAGCCCGGTAGGTGTCGACCTTGGTCGACAC

>NZ_CP040429|9|1|2127669-2127848|PILER-CR
GAGCCCGGTAGGTGTCGACCTTGGTCGACAC	AGCAGATCCAGACCATGCGTGGATGCCTCCCAATGCC
CCGCGCGGTAGAGCGCCAACCAAGGTTGGCG	GCTACCAGGGCGGTCGATCGAGGTTGACCGGCTGCGGCAGGCGTTCCTGGGAGCCCGGTAGGTGTCGACC
TTGGTCGACAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_154880240.1|2128005_2129517_+|lysine--tRNA-ligase	unknown	unknown	gnl|CDD|234778
NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase	unknown	unknown	gnl|CDD|235000
NZ_CP040429.1|WP_154880232.1|2119383_2120673_-|acyltransferase-family-protein	unknown	unknown	gnl|CDD|235167
NZ_CP040429.1|WP_154881339.1|2120870_2121713_+|LytTR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197918
NZ_CP040429.1|WP_032975476.1|2130862_2133034_+|response-regulator	unknown	unknown	gnl|CDD|274362
NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase	unknown	unknown	gnl|CDD|183918
NZ_CP040429.1|WP_025878945.1|2129720_2130866_+|two-component-system-response-regulator	unknown	unknown	gnl|CDD|225971
NZ_CP040429.1|WP_080148844.1|2114153_2115203_-|DUF1176-domain-containing-protein	unknown	unknown	gnl|CDD|369032
NZ_CP040429.1|WP_154880242.1|2133139_2134012_-|enoyl-CoA-hydratase	unknown	unknown	gnl|CDD|236338
NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter	unknown	unknown	gnl|CDD|376718
NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI	unknown	unknown	gnl|CDD|179115
NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|181546
NZ_CP040429.1|WP_154880230.1|2116538_2119445_+|DUF2135-domain-containing-protein	unknown	unknown	gnl|CDD|378008
NZ_CP040429.1|WP_154880236.1|2124501_2125893_+|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|143418
NZ_CP040429.1|WP_154880238.1|2125968_2127609_+|acetolactate-synthase-large-subunit	unknown	unknown	gnl|CDD|236239
NZ_CP040429.1|WP_154881338.1|2115356_2116406_-|DUF1176-domain-containing-protein	unknown	unknown	gnl|CDD|369032
NZ_CP040429.1|WP_099818762.1|2121803_2122929_+|peptide-chain-release-factor-2	unknown	unknown	gnl|CDD|136970
NZ_CP040429.1|WP_154880234.1|2123028_2123811_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|375319
NZ_CP040429.1|WP_154880228.1|2112355_2114113_+|single-stranded-DNA-specific-exonuclease-RecJ	unknown	unknown	gnl|CDD|182944
NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA	unknown	unknown	gnl|CDD|236445

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_154880240.1|2128005_2129517_+|lysine--tRNA-ligase	gnl|CDD|234778	PRK00484, lysS, lysyl-tRNA synthetase; Reviewed.	0
NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase	gnl|CDD|235000	PRK02106, PRK02106, choline dehydrogenase; Validated.	0
NZ_CP040429.1|WP_154880232.1|2119383_2120673_-|acyltransferase-family-protein	gnl|CDD|235167	PRK03854, opgC, glucans biosynthesis protein MdoC.	5.12858e-14
NZ_CP040429.1|WP_154881339.1|2120870_2121713_+|LytTR-family-transcriptional-regulator	gnl|CDD|197918	smart00850, LytTR, LytTr DNA-binding domain. This domain is found in a variety of bacterial transcriptional regulators. The domain binds to a specific DNA sequence pattern.	4.18939e-32
NZ_CP040429.1|WP_032975476.1|2130862_2133034_+|response-regulator	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	9.21026e-84
NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase	gnl|CDD|183918	PRK13252, PRK13252, betaine aldehyde dehydrogenase; Provisional.	0
NZ_CP040429.1|WP_025878945.1|2129720_2130866_+|two-component-system-response-regulator	gnl|CDD|225971	COG3437, COG3437, Response regulator containing a CheY-like receiver domain and an HD-GYP domain [Transcription / Signal transduction mechanisms].	1.10026e-132
NZ_CP040429.1|WP_080148844.1|2114153_2115203_-|DUF1176-domain-containing-protein	gnl|CDD|369032	pfam06674, DUF1176, Protein of unknown function (DUF1176). This family consists of several hypothetical bacterial proteins of around 340 residues in length. Members of this family contain six highly conserved cysteine residues. The function of this family is unknown.	2.39996e-95
NZ_CP040429.1|WP_154880242.1|2133139_2134012_-|enoyl-CoA-hydratase	gnl|CDD|236338	PRK08788, PRK08788, enoyl-CoA hydratase; Validated.	3.21987e-132
NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter	gnl|CDD|376718	pfam02028, BCCT, BCCT, betaine/carnitine/choline family transporter.	0
NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI	gnl|CDD|179115	PRK00767, PRK00767, transcriptional regulator BetI; Validated.	2.74043e-101
NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase	gnl|CDD|181546	PRK08751, PRK08751, long-chain fatty acid--CoA ligase.	0
NZ_CP040429.1|WP_154880230.1|2116538_2119445_+|DUF2135-domain-containing-protein	gnl|CDD|378008	pfam08487, VIT, Vault protein inter-alpha-trypsin domain. Inter-alpha-trypsin inhibitors (ITIs) consist of one light chain and a variable set of heavy chains. ITIs play a role in extracellular matrix (ECM) stabilisation and tumor metastasis as well as in plasma protease inhibition. The vault protein inter-alpha-trypsin (VIT) domain described here is found to the N-terminus of a von Willebrand factor type A domain (pfam00092) in ITI heavy chains (ITIHs) and their precursors.	2.01598e-30
NZ_CP040429.1|WP_154880236.1|2124501_2125893_+|aldehyde-dehydrogenase-family-protein	gnl|CDD|143418	cd07100, ALDH_SSADH1_GabD1, Mycobacterium tuberculosis succinate-semialdehyde dehydrogenase 1-like. Succinate-semialdehyde dehydrogenase 1 (SSADH1, GabD1, EC=1.2.1.16) catalyzes the NADP(+)-dependent oxidation of succinate semialdehyde (SSA) to succinate. SSADH activity in Mycobacterium tuberculosis (Mtb) is encoded by both gabD1 (Rv0234c) and gabD2 (Rv1731). The Mtb GabD1 SSADH1 reportedly is an enzyme of the gamma-aminobutyrate shunt, which forms a functional link between two TCA half-cycles by converting alpha-ketoglutarate to succinate.	0
NZ_CP040429.1|WP_154880238.1|2125968_2127609_+|acetolactate-synthase-large-subunit	gnl|CDD|236239	PRK08322, PRK08322, acetolactate synthase large subunit.	0
NZ_CP040429.1|WP_154881338.1|2115356_2116406_-|DUF1176-domain-containing-protein	gnl|CDD|369032	pfam06674, DUF1176, Protein of unknown function (DUF1176). This family consists of several hypothetical bacterial proteins of around 340 residues in length. Members of this family contain six highly conserved cysteine residues. The function of this family is unknown.	5.43528e-74
NZ_CP040429.1|WP_099818762.1|2121803_2122929_+|peptide-chain-release-factor-2	gnl|CDD|136970	PRK08787, PRK08787, peptide chain release factor 2; Provisional.	0
NZ_CP040429.1|WP_154880234.1|2123028_2123811_+|helix-turn-helix-domain-containing-protein	gnl|CDD|375319	pfam17765, MLTR_LBD, MmyB-like transcription regulator ligand binding domain. This domain is found in a family of actinobacterial transcription factors. The structure shows it has a PAS domain like fold and it is bound to Myristic acid.	1.1894e-42
NZ_CP040429.1|WP_154880228.1|2112355_2114113_+|single-stranded-DNA-specific-exonuclease-RecJ	gnl|CDD|182944	PRK11070, PRK11070, single-stranded-DNA-specific exonuclease RecJ.	0
NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA	gnl|CDD|236445	PRK09277, PRK09277, aconitate hydratase AcnA.	0

Protein sequences

>NZ_CP040429.1|WP_154880238.1|2125968_2127609_+|acetolactate-synthase-large-subunit
MSKGSDLLVAALENEGVERIFGIPGEENLDVVESLRHSSIELVITRHEQAAVFMAATYGRLTGKPGVCLATLGPGALNFTTGAAYALLGAWPVIMITGQKGIVASKQARFQIVDIVSTMKPLTKSARQIVSARTIPTIVREAFRTALEERPGPVLLELPEDIAAMEVEDVALIPPHPVDRPIASPEALDRAAQIIREAKRPLLVIASAASRPQSSEALSAFVLRAGIPFVTTQMGKGAVAGGSGLYMGTAALSERDYVHMAIDQADVIVTIGHEVTEKPPFVMRPGGRTVIHIGYSQAAVEQVYFPQVEVIGDIGRSLTLLADRIEGRVDNAATLLPLRATILEHIADRAEEAGFTPQRLVHDVRQVMPPDGIVALDNGMYKIWFARNYRTQVANTLLLDNALATMGAGLPSAIMASILYPQRRVLAVCGDGGFMMNSQELETARRLGLNLVVLILNDGAYGMIRWKQAVDGFADYGMTFGNPDFVKYAEAYGCQGHEVTAIEQFIPTLEAAFIAGGVHLVSVPVDYSENQRVLVDELRQAFPGNG
>NZ_CP040429.1|WP_154880236.1|2124501_2125893_+|aldehyde-dehydrogenase-family-protein
MSASPAAPAAISRDPATGQQIASHPFATDVELEAILDRGQAGFAAWSAQSLEQRASVLRAMAAVLRRDREPLAALATAEMGKVHAESLAEIEKCAVLCDWYADNGAAFLRDEPTAVADNKAYVSYLPLGVVLGIMPWNFPYWQVMRAAVPILMGGNGFLLKPAENIVGTAGLLAAAWRDAGLPDGTFIAANISREGTSAAIADDRIAAVTLTGSVAAGRSIAAQAGQALKKVVLELGGSDPFIVLADADLEAAVDAAVASRFQNTGQVCIAGKRIIVEDAVYERFVALFCERVQALTVGDGREAGNRIGPMARQDLLEQLDAQVRASVEAGAQLLVGGKQLDRPGSFYAPTVLAGVEPGMQAFDTETFGPVASISRARDADHAVELANKSEFGLSGNLWTGDHARAMQLARRLQTGGVFVNGFSASDPRVPIGGVKKSGFGRELSHFGIREFVNAQTVWFDRR
>NZ_CP040429.1|WP_154880234.1|2123028_2123811_+|helix-turn-helix-domain-containing-protein
MMRSEAERKDLGGFLKACRARVDPATLGLPAGRRRTPGLKREEVALAIGVSVSWYTWIEQGREVRASPEVLERLAQVLRLSDDERAYAFALSGYGVPLESPDETVTDGLRQLVEAMQPIPAYVRNTRFDILAWNPAIADLFVDYGQLAPHERNTLRLMFLYPPYRTLILNWEEMTRGLLASFRAAMAQAPDKAPFLALAEDIGAHSEQFRQWWPEHDVRRFDEGAKKLNHPTRGLLDLQYVALVPESRHDLSLVTYLPRR
>NZ_CP040429.1|WP_099818762.1|2121803_2122929_+|peptide-chain-release-factor-2
MIELNPVRQRIADLTDRVLSLRGYLDYDAKKERLEEVTRELESPDVWNNAEYAQNLGRERSTLEKTVGGIAAVLEGLSDATELLELAESEQDEDTALAVVADLDKHQAHVEKLEFQRMFSGQMDTAPAFVDIQAGAGGTEAQDWAEILLRMYLRWCESRGWKTELMEVSGGDVAGIKSATLRVEGDYAYGWLKTETGVHRLVRKSPFDSDNRRHTSFTSVFVSPEVDNNIEIDINPADLRTDVYRSSGAGGQHVNKTESAVRITHIPTNTVVACQTGRSQHQNRDNAMKMLAAKLYELEIQKRNAERDAVEATKSDIGWGSQIRNYVLDQSRIKDLRTGIERSDTQKVLDGDLDEFVEASLKAGLAVGSKRIDA
>NZ_CP040429.1|WP_154881339.1|2120870_2121713_+|LytTR-family-transcriptional-regulator
MGNGRQGRQAAVFWVVLFLGTAAANVLAKAMMAARDELPSQWMAATIDEFSSALVSLLLLAVLIRAASRWPLHTDTWRQRLVPYLLGAVAWWLLHVSAMVLLRKAAHAVLGSHYTFGDWPAQWFYEFFKDIQTYALLVSAVHALAWFGRRRQGEATLLAAPDEGPPVEPVDRPDHFLVRKLGKEFLVATADVEYAQAAGNYVNLRVRGHDYPLRITMAVLEARLDPVLFLRSHRSWLVNRDQLRSIEPLDGGEALLHMADGAKVPCSRRQLPLLRQALGG
>NZ_CP040429.1|WP_154880232.1|2119383_2120673_-|acyltransferase-family-protein
MTRRHDLDTLRIGAFGLLILYHVAMAYVAGWDFHLKSVHTAEWLQWPMIALNRWRMPLLFAISGIALGLCLPAQGRWRFALRRGGRLLLPLLFGIVAVVSLQAYCEAVDKGDVTPGLGAFLWRYWQFRPWPGASFTGAAYGFTWNHLWYLAYLIPYTLLAILLASVVRPLRHRLPGLPAGDRWVATLGLLLPVLWLAWALLVILPAHPPTHALVDDLYVHAEWLPLFLGGFLAARWQRGWDLLVRGRRLTLVLAVVGLAVELGIRALGRMPDLGDLPQWVLALPWAQTERVGRALYTWCSLLALFGWAQVLLARPWRGLGYCREAVFSWYILHQTVLIMLLYWLRPLQLGAWLEPALVIVGTVAGCLLIHELLVRRVRWLRPLFGLRADRNGAVSITQDHSAGRRAWPGATAPRTRQPAPSRHDPSAAS
>NZ_CP040429.1|WP_154880230.1|2116538_2119445_+|DUF2135-domain-containing-protein
MVFARCCAVLLLALAAWPVGAQAPRIARPQATTPLLIAPAAEQPVQLRHARIEGEVQAGIAQTRITLEFHNPNQRVLEGELQFPLAEGQQITGFALDINGELREAVPVPKDRGRQVFEEIARRGVDPGLLEQTAGNQFRLRVYPLPAGGSRRVQLVVREPLAYAGQGWRWTLPLQFVAGAAAVELDVRAPKGAEAGSAPFRIADGRLHWQGRGAQLPAQLQWTLPAERKAQVQVARWQDGHYLLAQLPVPTSTAPRRVPSEVGLLWDGSGSAGQRDRTREFALLDRYFAAMGEGNVALTVLRDRAEPVRHFRIRSGDWSELRRALMAVQPDGASALAQWQPQPSVKEYLMVSDGLLTYGPEALPALAADQRLFAVSSAGARTDATRLRGWSEAHAGSFVALGSDIDAAARELLSMPLDVQIDAGRGVQDVVVDRRSQAQGWLWLHARLAAEGVPMRVRIAGGQWQALPESSTSADGDLLAGLWAQARLQQLSTDRRGNREAMQRLSQQFSLVGPDTSLIVLETLDDYLRYAIRPAGALRAQYDQRFARQVADRDAADRQRLDKVVTQWQQRQQWWSRRWPKGMRVQAKALEVVGQDAYAAAPVAMLAAPPPAPAPMAVAAEQRAESSSARARRSPPRQAPAGLEAAMDAVAIEPTASNAPAAANDGQLGIRLAAWQSDSPVARRLRQGPSSQLYDRYLAERAANANSSAFFLDVADLLIEQGQRDLALRVLSNLAEMELDNRHLLRVLGYRLLQADAPALAVPVFEQVLAMGQEEPQSFRDLGLALAAAGKPQQALAPLYQVVVRPWDGRFDGIALIALDELTNLVAGSKPRLDTTGIDPRLLQAMPLDLRVVLAWDADNSDMDLWVTDPNGERAYYGNRLTYQGGQMSQDFTGGYGPEQFSLRNAKPGKYKVEANYFGSRQQLVTGATTLMLRLTTHWGTPKQKDQMITMRLKDRAETVLVGEFEVR
>NZ_CP040429.1|WP_154881338.1|2115356_2116406_-|DUF1176-domain-containing-protein
MSPPQLALLLALSGPIATAAADSREGLFYQHRDWVVACDNTRTCRAAGYSGSNASPLSVLLTRSGGPNQAVQGRLALHPDEGQTQLNEVLNLRIQEQDLGILAPDTVPGMYSLSATQTSALLSAMVGDGGIMVTDASDQRWPLSDKGASAVLLKIDEYQGRLGTPGAMLRTGRSPEASVPAALPIPVIRKASTLDAMSEDPAFATTAASPALRAALLATLKEPRCAGLLAASPDLPISNSPLKVQRLDARHLIVSVPCWRAASNDGDGYWVIRERPPYLPIWVTNDAYRYEGGQIFAYVRGLGPVDCTSEYTWTWDGTRFIHTSAIEGVICAQTPDGIWKLPTRISEVH
>NZ_CP040429.1|WP_080148844.1|2114153_2115203_-|DUF1176-domain-containing-protein
MRSPLLPTLLALCWPLAAGAVDAPAGLYFQHHDWVVACDNTRTCRAAGYASGDDSTLSVLLTRAGGPNQAISGRMSLQPIDDQPQPKGALHLRIQQRDLGVLAPATEPGVHVLSAAQTSAVLSALVRDGGIAVVDGAGHTWPLSDKGAAAVLLKTDEFQGRVGTPGAVMRKGAAAESSVPAAVAKPVVRKAPTLSTPPDDPAFSKLAASPALRAALRATLVEPSCEGLLDTDPDLPISNSPLQIQRLDTKHLLVNVPCWRAAYNTGDGYWVIGENAPYQPQWVTSDAIDYGDGQIVASHKGRGLADCVSDETWTWDGTRFVATSAISGGLCRGVPGGTWELPTRVTDVR
>NZ_CP040429.1|WP_154880228.1|2112355_2114113_+|single-stranded-DNA-specific-exonuclease-RecJ
MSLAADAALPSSDTPMIRRRDAVAPGSWPEGTLPLLARLYAARGAHTPELALPKLGNLHAPELLTGIDAAVDLLVQAIAADKRILVVGDFDCDGATACAVGVRGLRMLGAQHVFHAVPNRMVHGYGLSPSLVDELAALQPDLLVTVDHGIACHAGVTAAKARGWQVLVTDHHLPGPLLPPADVIVDPNLDGDAFPSKALAGVGVIFYVLMALRRQMREAGVFADGKGPDLTTLLDLVAVGTVADLVVLDANNRALVSAGLRRLRNGQGCVGLKALIEASGRDAARLTATDIGFGLGPRLNAAGRLEDMALGIALLLTEDPRQARDIAQTLEQINAERRAVQQSMTDDAEHALSRVVLDTAGRRPVAACLFDADWHPGVVGLVASKMKDRLHRPVIAFAPAEPGADTLRGSARSIAGLHIRDALALVDARHPGLIERFGGHAMAAGLSMRLDHLATFEAAFVATVLEMLDPAALQQQVLSDGELAADELDHRHADALRLAGPWGQGFPEPLFDGHFEVANWRVLKERHLKLELRLPGVPGTINAIHFGGWHGNAPGRHVHLAYRLACDDYRGGAAIQLIVEHCLPA
>NZ_CP040429.1|WP_154880240.1|2128005_2129517_+|lysine--tRNA-ligase
MSEATDTPPVDENKLIAERREKLKALRGQGIAYPNDFRREDFAGSLQEEFADAEQWTAETLEGNGRQVKMAGRLMAKRVMGKASFAQIQDESGRIQLFLQGSVLGDAYTAFKGWDVGDIIAVEGGLTRTKTGELSVKAESIRLLTKSLRPLPDKWHGLADVEQRYRQRYVDLIVTPESRAVFIKRSKIIRAMRAWLDNRDFLEVETPMMHYIPGGAAAKPFTTHHNALDLDLYLRVAPELYLKRLTVGGLERVYEINRNFRNEGVSTRHNPEFTMMELYEAYATYNEIMDLTEGVIRDVAQSVNGSTVVEWDGANIDLGPAFRRWRMDEAVRHHNPEISAADCTDRDALLRHCERLKIRVKPSYGWGKLLLEIFEATVEHTLIQPTFITDHPVEVSPLARANDNDPGYTDRFELFVNGKELANGFSELNDPEDQAQRFQAQVAAKEGGDDEAMHYDADYIRALEYGMAPTGGLGIGVDRLVMLLTGSSSIRDVLLFPYMRPEQ
>NZ_CP040429.1|WP_025878945.1|2129720_2130866_+|two-component-system-response-regulator
MQGASVHSGGVSSPADLSAWSRKQAENALNIVIVDDQTSARTMLRHVIEDIAPELSVHDFGDPLTALAWCESYPVDLLLLDYRMPEMDGLEFARRFRRLPKHRDIPVILITVVGDEPIRQAALEAGVIDFLVKPIRPRELRARCYNLLQLRQQTENVKQRALSLEQRLLASMHEVEERERETLSRLARAIEFRDAGTSAYLERMARVAGLIAEQLGLPEDDVKLIEMAAPLHDMGKIAIPDAVLLKQGKLNDEELAIMRRHPRIGHELLSGSQNRFIQVGALIALRHHERYDGSGYPDGLVGDAIPLEARIVAVADVFDALISPRPYKEAWTMEATMAYLYAQRGRLFDPRCVDALLRGREQLEQICAEHSTASARPGLGA
>NZ_CP040429.1|WP_032975476.1|2130862_2133034_+|response-regulator
MKRLLSRLRLRLSQRQDSEHGQQIVRIVLISLILAYVLLPSARHDLPHTQYVGVLAIVLTGLSLSLLLFGWLLWRPQRSDPRRVLGMLADYGLIAAGMIQMGEPLSWVYIVVMWVTVGNGMRFGNHYLYVAVAMAMVSFGSTALSTPYWQQNARLAIGLWLGLAAVPLYFSTLLRQLTEAMAEARRASEAKSRFLANMSHEFRTPLNGLNGMTEVLATTRLDDEQRECVSTIQASSRSLLALVEEVLDISAIEAGKLRVVAEDFVLSEVMQAIGLILLPQAKAKRLDYRVKVAETVPPTLRGDVGHLRQILLNLAGNAVKFTDHGRVEIRVSVVHADTQGGVRLRFDILDTGIGVAPAMRPRLFEAFEQADVSMARRHEGTGLGTTIAKGLVEAMDGEIGYLDNPPQGSHFWVELPFAPPQPVVPGAVPTLAAGDETGAGGNVIAFADPFLRHRARVRSMQILVADDHEANRMVLQRLLQKAGHKVLCVDGGEAVLDALAESEFDAAIVDLHMPGMSGLDMLKELRVMQAGGGPRTPVLVLSADVTPEAIQRCTQAGAHAFLAKPVVAVRLLDTLAEIANNAQLKASAPPIVRTVTNLDGVLDTGVLDELASLGMGEGFEREFIRQCLDDAESCLRKAEGDGEAARWGAFREQSHAIKGVASNLGLVRASNRAGELMRMADWQLKAEWRQRLAVLQGAIKEGRQALDARAERKARGVADDGER
>NZ_CP040429.1|WP_154880242.1|2133139_2134012_-|enoyl-CoA-hydratase
MSTIEKLPSSGSPYATIRTQDSADGAAHWLFMHADASTGVRPCCRKDMLDEMWSYMSAITRGPAQRHSGQLRHFVLASDAAAYNLGGDLDLFTRLIREGNRDLLLTYAQRCVEGVHHLHTGFGGDVRSIALIQGDALGGGLEMALACHTIVAEEGCGMGLPEVLFGLFPGMGAYSFLCRRVAPQLAEKIILDGRIYSAEAMHAMGVVDVLVRKGEGRGAVEEMIRQQQRLPQSYLAMNAARNLAQAVSYDELLEITKVWVDSALALGDRSLRTMDRLIKAQTRRANLDVA
>NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase
MSLDRPWLQSYPKGVPAEIDVNEFHSVVSVFDASVAKYRDRPAYSSFGKTLTYGETDALVEQFAAYLLGELKLKKGDRVALMMPNCLQYPIATFGVLRAGLTVVNVNPLYTARELKHQLVDAGVTALVVVDNFGDTVEQVIADTQVKQVITTGLGDLLGAKGTIVNFVLKYVKKMVPNYHLKGAIRFKQALKLGSRHTLPKVEIDHDDVAFLQYTGGTTGVAKGAMLTNRNLIANMQQASAWISASGIEMGKEWIITALPLYHIFALTANGLVFMKFGGCNHLITNPRDMKGFVKELKSVRFTAITGVNTLFNGLLNTPGFDTVDFSSLKVTLGGGMAVQRAVAERWKKTTGVTLVEAYGLTETSPAACINPLTLAEYNGSIGLPIPSTDACIKDDNGNILALGEVGELCIRGPQVMKGYWQRPEETAKAIDADDWLHTGDMAKMDEHGFFYIVDRKKDMILVSGFNVYPNEVEDVIAMMPGVLEVAAVGVPDEKSGEVVKVVIVKKDPNLTAEMVKEHARANLTGYKHPRIVEFRKELPKTNVGKILRRELRDTPAP
>NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase
MSTHNEYDYIIIGAGSAGNVLATRLTEDADVSVLLLEAGGPDYRLDFRTQMPAALAFPLQGKRYNWAYKTDPEPFMNNRRMDCGRGKGLGGSSLINGMCYIRGNAMDYDNWAGMPGLEDWTYLDCLPYFRKAETRDIGPNDYHGGDGPLRVTTPKAGNNELFAAMVEAGVQAGYPRTDDLNGYQQEGFGPMDRTVTPKGRRSSTARGYLDLAKPRPNLTIVTHALTDRILFSGKRAVGVQWLHNDQPQRATARREVLLCGGAIASPQILQRSGVGPADLLRSLDIDLVHHLPGVGANLQDHLEMYLQYECKKPVSLAPALKLYNQPAIGAEWLFLGTGIGASNQFEAGGFIRSDAEFDWPNLQYHFLPVAINYNGSNPIKAHSFQMHVGSMRSPSRGRIHVRSKDPREDPSILFNYMSHDQDWREFRSAIRITREIFAQPALAPYSGREISPGSALQTDTQIDAFVREHAETAYHPSCSNKMGHADDPMAVVDGQGRVHGLEALRIVDASIMPQVVTGNLNAPTIMIAEKLADVIRGRAPLPRSTASYYKANGAPVRNKS
>NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase
MTTLPVQQLYIHGRRVDATSGKTFQTVNPANGQVLADVQIASQADVERAVESASEGQKVWAAMTAMERSRILRRAVEILRERNDELAHLETLDTGKALAETTTVDIVTGADVLEYYAGLATAIEGIQLPLRESSFFYTRREPLGVVAGIGAWNYPIQIAMWKSAPALAAGNAMVFKPSEVTPLTAIKLAEIYTEAGVPDGVFNVVQGPGREIGNWLTEHPVIEKISFTGGVATGKKVMASAASSSLKEVTMELGGKSPLVICDDADLDRAADIAVMANFFSSGQVCTNGTRVFVPRSMLAAFEAAVVERVKRIRIGDPMAAETNFGPLTSFPHMENVLRFIESGKSEGARLLTGGGRATDGALAEGAYVLPTVFSDCRDDMTIVREEIFGPVMSILAYDDEDEVVRRANDTTFGLAAGVVSKDISRAHRIIHRLEAGICWINTWGESPAEMPVGGYKQSGVGRENGISTLGHYTRIKSVQVELGDYASVF
>NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI
MPKKGVEPVRREQLIRATFQTIDEIGMADATVATIARKAGLSSGIVAHYFGDKDGLLNAAMRQILRELKAAVARYRDAAAGDARSQLRAIVDGNFDDSQTNGTAMRVWLTFWAASMHQPELARLQRANDQRLFSNLCHQFNRQLPHAQARLSARGLAAMIDGLWLRGSLVGGDFNADKARRIAYGYIDFQLQANAP
>NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter
MSSLAHPKRSPLRLNRFVFFSSSVSIGILGALTVFFPEASEHWLQWAQAEVSAAFGWWYMLLIVACLGFVLWLAFSPYGRIRLGHNEESPAFGYVAWVSMLFSAGIGIALLYYGAYEPLDHFLNPPGQPGGTVAAGREAMVLTFLHWGLHGWALYALVGVALGYFAYRRNLPLALRSALYPIFGERIHGRIGDMVDGFGILATLISMVTNLGIGALVVQSGLVYLFHIPDTPQVLVAIVLVMMVVATIGVVAGVEKGIAWLSNLNVRLLCLLLLFVLVTGPTLHLFDGLVQNTGDYLGAFVRKSFDMYLNDPKGREWMGSWTLFYWAWWIAWAPFVGLFVARISRGRTIREVIMGVLLIPLGFTLAWLSIFGNTAIDLVLNHGQAVLGQVAQHDAAMTLFKLLEYLPAAPYIAGAAVVIGFVLFLTPVDSGTLMIANLCTRRVDDGVEDGHDAPIWLRVFWAAGITVASVGLLLAGNFSAMQTAVVLCGLPFSLILAFYMWGLLKALRTDPDAPRR
>NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA
MSDSFSTRSQLDVGGKTYDYFSLPKLGQRFDISHLPYSMKILLENLLRHEDGGVTVGKDHIEAVARWQPSAEPDTEIAFMPARVVLQDFTGVPCVVDLAAMRDAVVKLGGRPEQINPLIPSELVIDHSVQVDVFGKPDALDLNGKIEFQRNQERYGFLRWGQKAFDNFKVVPPNTGIVHQVNLENLARVVMTADKDGKAVAYPDTVFGTDSHTTMINGIGVLGWGVGGIEAEAAMLGQPSSMLIPQVVGFKLTGKLPEGATATDLVLTVTQMLRKLGVVGKFVEFYGDGLQHLPLADRATIGNMAPEYGATCGIFPIDNESLTYLRLSGRSEEQIALVEAYAKAQGLWHDANSPHAQYSTTLELDMGTVKPSLAGPKRPQDRVLLEDVQKNYRDALVGMTANRDKRSEDVSTFVNEGGGAAVGNEQLAKGYADIEMDGRKVRLKDGAVVIAAITSCTNTSNPAVMIGAGLLARNAAAKGLDRKPWVKTSLGPGSRVVTDYLEKAGVLTELEKIGFYVVGYGCTTCIGNSGPLPTEVSAGIASGDLVVTSVLSGNRNFEGRVHPEVKMNYLASPPLVVAYAIAGTTDIDLTTEPLGIGSDGQPVYLRDIWPSNKEIGDVIAATVGPEMFKQNYADVFKGDTRWNTIASPDGDLYEWSDASTYIKNPPYFDGMTMQVGTIDDVHGARVMGLFGDSITTDHISPAGNIKKDSPAGRFLQERGVQPADFNSYGSRRGNDDVMVRGTFANIRIKNLMFGGEEGGNTLYYPANGGQPEKLAIYDAAMKYKADKVPLVVLAGKEYGTGSSRDWAAKGTLLLGVKAVIAESFERIHRSNLVGMGVLPLQFRNGENAQSLGLDGSEVIDVTGLQDGASKRATVTATKADGTKKTFEVSVMLLTPKEVEYFRHGGLLQYVLRQLAGR

Crispr_ID: NZ_CP040429_10

• CRISPR_ID: NZ_CP040429_10
• CRISPR_location: 2148960-2149072
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_10

Consensus_repeat	Method
GGTAGTGCCGGCCGCTGGCCGGCAGCC	CRISPRCasFinder

spacers of NZ_CP040429_10

>10.1|2148987|59|NZ_CP040429|CRISPRCasFinder
CGTTGAAACGAAGAACCCCCGGTGAGAGCCGGGGGTTTTTTGTGGTGCCGATGATGCCT

CRISPR arrays and Neighbor proteins around NZ_CP040429_10

CRISPR arrays

The CRISPR arrays of NZ_CP040429_10

>merge|NZ_CP040429|10|2148960-2149072|CRISPRCasFinder
GGTAGTGCCGGCCGCTGGCCGGCAGCCCGTTGAAACGAAGAACCCCCGGTGAGAGCCGGGGGTTTTTTGTGGTGCCGATGATGCCTGGTAGTGCCGGCTGCTGGCCGGCAGCC

>NZ_CP040429|10|9|2148960-2149072|CRISPRCasFinder
GGTAGTGCCGGCCGCTGGCCGGCAGCC	CGTTGAAACGAAGAACCCCCGGTGAGAGCCGGGGGTTTTTTGTGGTGCCGATGATGCCT
GGTAGTGCCGGCTGCTGGCCGGCAGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter	unknown	unknown	gnl|CDD|376718
NZ_CP040429.1|WP_025878967.1|2160156_2160648_-|chemotaxis-protein-CheW	unknown	unknown	gnl|CDD|182587
NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase	unknown	unknown	gnl|CDD|235000
NZ_CP040429.1|WP_154880253.1|2154379_2156644_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|185001
NZ_CP040429.1|WP_025878954.1|2145130_2145502_-|outer-membrane-protein-assembly-factor-BamE	unknown	unknown	gnl|CDD|225465
NZ_CP040429.1|WP_032975462.1|2153477_2154347_-|chemotaxis-protein-CheR	unknown	unknown	gnl|CDD|236725
NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA	unknown	unknown	gnl|CDD|236445
NZ_CP040429.1|WP_033831025.1|2157161_2159537_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|185001
NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase	unknown	unknown	gnl|CDD|183918
NZ_CP040429.1|WP_134832495.1|2149136_2150087_-|hypothetical-protein	unknown	unknown	gnl|CDD|236733
NZ_CP040429.1|WP_025878955.1|2145692_2145917_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	unknown	unknown	gnl|CDD|198034
NZ_CP040429.1|WP_025878966.1|2159635_2160019_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI	unknown	unknown	gnl|CDD|179115
NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|181546
NZ_CP040429.1|WP_049466025.1|2145923_2146325_+|type-II-toxin-antitoxin-system-VapC-family-toxin	unknown	unknown	gnl|CDD|224404
NZ_CP040429.1|WP_099783897.1|2151814_2152888_-|chemotaxis-response-regulator-protein-glutamate-methylesterase	unknown	unknown	gnl|CDD|234828
NZ_CP040429.1|WP_025878968.1|2161038_2161812_-|flagellar-brake-protein	unknown	unknown	gnl|CDD|377813
NZ_CP040429.1|WP_025878962.1|2152884_2153481_-|chemoreceptor-glutamine-deamidase-CheD	unknown	unknown	gnl|CDD|237396
NZ_CP040429.1|WP_154880251.1|2150131_2151727_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154880249.1|2146366_2148958_+|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase	unknown	unknown	gnl|CDD|236424

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter	gnl|CDD|376718	pfam02028, BCCT, BCCT, betaine/carnitine/choline family transporter.	0
NZ_CP040429.1|WP_025878967.1|2160156_2160648_-|chemotaxis-protein-CheW	gnl|CDD|182587	PRK10612, PRK10612, chemotaxis protein CheW.	6.0909e-63
NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase	gnl|CDD|235000	PRK02106, PRK02106, choline dehydrogenase; Validated.	0
NZ_CP040429.1|WP_154880253.1|2154379_2156644_-|HAMP-domain-containing-protein	gnl|CDD|185001	PRK15041, PRK15041, methyl-accepting chemotaxis protein.	7.37111e-109
NZ_CP040429.1|WP_025878954.1|2145130_2145502_-|outer-membrane-protein-assembly-factor-BamE	gnl|CDD|225465	COG2913, OlmA, Outer membrane lipoprotein OmlA (small protein A) [Cell envelope biogenesis, outer membrane].	8.12008e-05
NZ_CP040429.1|WP_032975462.1|2153477_2154347_-|chemotaxis-protein-CheR	gnl|CDD|236725	PRK10611, PRK10611, protein-glutamate O-methyltransferase CheR.	1.22279e-111
NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA	gnl|CDD|236445	PRK09277, PRK09277, aconitate hydratase AcnA.	0
NZ_CP040429.1|WP_033831025.1|2157161_2159537_-|HAMP-domain-containing-protein	gnl|CDD|185001	PRK15041, PRK15041, methyl-accepting chemotaxis protein.	1.57607e-105
NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase	gnl|CDD|183918	PRK13252, PRK13252, betaine aldehyde dehydrogenase; Provisional.	0
NZ_CP040429.1|WP_134832495.1|2149136_2150087_-|hypothetical-protein	gnl|CDD|236733	PRK10672, PRK10672, endolytic peptidoglycan transglycosylase RlpA.	0.00420971
NZ_CP040429.1|WP_025878955.1|2145692_2145917_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	gnl|CDD|198034	smart00966, SpoVT_AbrB, SpoVT / AbrB like domain. This domain is found in AbrB from Bacillus subtilis. The product of the abrB gene is an ambiactive repressor and activator of the transcription of genes expressed during the transition state between vegetative growth and the onset of stationary phase and sporulation. AbrB is thought to interact directly with the transcription initiation regions of genes under its control. AbrB contains a helix-turn-helix structure, but this domain ends before the helix-turn-helix begins. The product of the B. subtilis gene spoVT is another member of this family and is also a transcriptional regulator. DNA-binding activity in this AbrB homologue requires hexamerisation. Another family member has been isolated from the Sulfolobus solfataricus and has been identified as a homologue of bacterial repressor-like proteins. The Escherichia coli family member SohA or Prl1F appears to be bifunctional and is able to regulate its own expression as well as relieve the export block imposed by high-level synthesis of beta-galactosidase hybrid proteins.	2.21392e-08
NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI	gnl|CDD|179115	PRK00767, PRK00767, transcriptional regulator BetI; Validated.	2.74043e-101
NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase	gnl|CDD|181546	PRK08751, PRK08751, long-chain fatty acid--CoA ligase.	0
NZ_CP040429.1|WP_049466025.1|2145923_2146325_+|type-II-toxin-antitoxin-system-VapC-family-toxin	gnl|CDD|224404	COG1487, VapC, Predicted nucleic acid-binding protein, contains PIN domain [General function prediction only].	9.00481e-13
NZ_CP040429.1|WP_099783897.1|2151814_2152888_-|chemotaxis-response-regulator-protein-glutamate-methylesterase	gnl|CDD|234828	PRK00742, PRK00742, chemotaxis-specific protein-glutamate methyltransferase CheB.	0
NZ_CP040429.1|WP_025878968.1|2161038_2161812_-|flagellar-brake-protein	gnl|CDD|377813	pfam07317, YcgR, Flagellar regulator YcgR. This domain is found N terminal to pfam07238. Proteins which contain YcgR domains are known to interact with the flagellar switch-complex proteins FliG and FliM. This interaction results in a reduction of torque generation and induces CCW motor bias.	1.77222e-31
NZ_CP040429.1|WP_025878962.1|2152884_2153481_-|chemoreceptor-glutamine-deamidase-CheD	gnl|CDD|237396	PRK13487, PRK13487, chemoreceptor glutamine deamidase CheD; Provisional.	8.75355e-124
NZ_CP040429.1|WP_154880249.1|2146366_2148958_+|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase	gnl|CDD|236424	PRK09238, PRK09238, bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase; Validated.	0

Protein sequences

>NZ_CP040429.1|WP_154880249.1|2146366_2148958_+|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase
MLEAYRHHVAERAALGIPPLPLTAQQTADVIELLKNPPQGEAEFLLDLLTHRVPAGVDDAAKVKASYLAAIALGSEQNPLISRERATELLGTMLGGYNVAPLVQLLDDVSVGAIAADALKKTLLVFDAFHDVQEKAKAGNANAQAVMQSWADAEWFTSNPEVPQSLTVTVFKVPGETNTDDLSPAPDATTRPDIPMHALAMLKNKRDDAAFTPEEDGKRGPIQQILSLKDKGHLVAYVGDVVGTGSSRKSATNSVLWWTGDDIPYIPNKRAGGVCLGSKIAPIFYNTMEDAGALPIELDVSKMEHGDVVELRPYDGKALKNGEVIAEFQVKSEVLFDEVRAGGRIPLIIGRGLTGKAREALGLAPTDLFRLPVQPADTGKGFSLAQKMVGRACGLPEGQGMRPGTYCEPKMTSVGSQDTTGPMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDVKTHHTLPEFISTRGGVSLRPGDGVIHSWLNRMLLPDTVGTGGDSHTRFPVGISFPAGSGLVAFAAATGVMPLDMPESVLVRFKGKMQPGVTLRDLVNAIPLYAIKSGLLTVAKAGKKNIFSGRILEIEGLPELKVEQAFELSDASAERSAAGCSVRLNKEPIIEYLTSNITLLKWMIAEGYQDPRSLQRRIEKMEAWLANPELLEPDADAEYAAVIEIDLADIHEPIVACPNDPDDVKTLSEVAGAKIDEVFIGSCMTNIGHFRAAAKLLEGKRDLPTRLWVAPPTKMDASELTKEGVYGTFGATGARMEMPGCSLCMGNQAQIREGSTAMSTSTRNFPNRLGRNTNVYLGSAELAAICSRLGRIPTKEEYMADIGVIAASGSEIYRYMNFDQIEEYQDVANTVAA
>NZ_CP040429.1|WP_049466025.1|2145923_2146325_+|type-II-toxin-antitoxin-system-VapC-family-toxin
MIAVDSPVLVELLSNGPQADAVEACLRQSLVGGRVVVCGATLAEICAALRGGAEVLEALEEMGVHFNALEAKSALRAGEMHRRHRQRGGSQRRGLDEFMIGAHALLQCDGLITWNDTFYRDYFKGLKLIVPQA
>NZ_CP040429.1|WP_025878955.1|2145692_2145917_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein
MEATVAERGQITLPKAVRDALGLTKGTLLKVELEGSRIILRKSVDDAISRARGKFSLDGFESADAAVRDLRDEE
>NZ_CP040429.1|WP_025878954.1|2145130_2145502_-|outer-membrane-protein-assembly-factor-BamE
MRALALALILAAPLAVSTTSAHANPFGAYTTGIEITQQQMDTLEVGKTTQDNIREKFGAPGRREQLGDTQVWYYDFVKIKSFGKNIQEATVLEFNKQGVLTAKSKSNAVGKTGNPLIDAANGK
>NZ_CP040429.1|WP_154880247.1|2142119_2144873_-|aconitate-hydratase-AcnA
MSDSFSTRSQLDVGGKTYDYFSLPKLGQRFDISHLPYSMKILLENLLRHEDGGVTVGKDHIEAVARWQPSAEPDTEIAFMPARVVLQDFTGVPCVVDLAAMRDAVVKLGGRPEQINPLIPSELVIDHSVQVDVFGKPDALDLNGKIEFQRNQERYGFLRWGQKAFDNFKVVPPNTGIVHQVNLENLARVVMTADKDGKAVAYPDTVFGTDSHTTMINGIGVLGWGVGGIEAEAAMLGQPSSMLIPQVVGFKLTGKLPEGATATDLVLTVTQMLRKLGVVGKFVEFYGDGLQHLPLADRATIGNMAPEYGATCGIFPIDNESLTYLRLSGRSEEQIALVEAYAKAQGLWHDANSPHAQYSTTLELDMGTVKPSLAGPKRPQDRVLLEDVQKNYRDALVGMTANRDKRSEDVSTFVNEGGGAAVGNEQLAKGYADIEMDGRKVRLKDGAVVIAAITSCTNTSNPAVMIGAGLLARNAAAKGLDRKPWVKTSLGPGSRVVTDYLEKAGVLTELEKIGFYVVGYGCTTCIGNSGPLPTEVSAGIASGDLVVTSVLSGNRNFEGRVHPEVKMNYLASPPLVVAYAIAGTTDIDLTTEPLGIGSDGQPVYLRDIWPSNKEIGDVIAATVGPEMFKQNYADVFKGDTRWNTIASPDGDLYEWSDASTYIKNPPYFDGMTMQVGTIDDVHGARVMGLFGDSITTDHISPAGNIKKDSPAGRFLQERGVQPADFNSYGSRRGNDDVMVRGTFANIRIKNLMFGGEEGGNTLYYPANGGQPEKLAIYDAAMKYKADKVPLVVLAGKEYGTGSSRDWAAKGTLLLGVKAVIAESFERIHRSNLVGMGVLPLQFRNGENAQSLGLDGSEVIDVTGLQDGASKRATVTATKADGTKKTFEVSVMLLTPKEVEYFRHGGLLQYVLRQLAGR
>NZ_CP040429.1|WP_059064113.1|2140303_2141854_+|BCCT-family-transporter
MSSLAHPKRSPLRLNRFVFFSSSVSIGILGALTVFFPEASEHWLQWAQAEVSAAFGWWYMLLIVACLGFVLWLAFSPYGRIRLGHNEESPAFGYVAWVSMLFSAGIGIALLYYGAYEPLDHFLNPPGQPGGTVAAGREAMVLTFLHWGLHGWALYALVGVALGYFAYRRNLPLALRSALYPIFGERIHGRIGDMVDGFGILATLISMVTNLGIGALVVQSGLVYLFHIPDTPQVLVAIVLVMMVVATIGVVAGVEKGIAWLSNLNVRLLCLLLLFVLVTGPTLHLFDGLVQNTGDYLGAFVRKSFDMYLNDPKGREWMGSWTLFYWAWWIAWAPFVGLFVARISRGRTIREVIMGVLLIPLGFTLAWLSIFGNTAIDLVLNHGQAVLGQVAQHDAAMTLFKLLEYLPAAPYIAGAAVVIGFVLFLTPVDSGTLMIANLCTRRVDDGVEDGHDAPIWLRVFWAAGITVASVGLLLAGNFSAMQTAVVLCGLPFSLILAFYMWGLLKALRTDPDAPRR
>NZ_CP040429.1|WP_025878951.1|2139542_2140133_-|transcriptional-regulator-BetI
MPKKGVEPVRREQLIRATFQTIDEIGMADATVATIARKAGLSSGIVAHYFGDKDGLLNAAMRQILRELKAAVARYRDAAAGDARSQLRAIVDGNFDDSQTNGTAMRVWLTFWAASMHQPELARLQRANDQRLFSNLCHQFNRQLPHAQARLSARGLAAMIDGLWLRGSLVGGDFNADKARRIAYGYIDFQLQANAP
>NZ_CP040429.1|WP_105163996.1|2138028_2139501_-|betaine-aldehyde-dehydrogenase
MTTLPVQQLYIHGRRVDATSGKTFQTVNPANGQVLADVQIASQADVERAVESASEGQKVWAAMTAMERSRILRRAVEILRERNDELAHLETLDTGKALAETTTVDIVTGADVLEYYAGLATAIEGIQLPLRESSFFYTRREPLGVVAGIGAWNYPIQIAMWKSAPALAAGNAMVFKPSEVTPLTAIKLAEIYTEAGVPDGVFNVVQGPGREIGNWLTEHPVIEKISFTGGVATGKKVMASAASSSLKEVTMELGGKSPLVICDDADLDRAADIAVMANFFSSGQVCTNGTRVFVPRSMLAAFEAAVVERVKRIRIGDPMAAETNFGPLTSFPHMENVLRFIESGKSEGARLLTGGGRATDGALAEGAYVLPTVFSDCRDDMTIVREEIFGPVMSILAYDDEDEVVRRANDTTFGLAAGVVSKDISRAHRIIHRLEAGICWINTWGESPAEMPVGGYKQSGVGRENGISTLGHYTRIKSVQVELGDYASVF
>NZ_CP040429.1|WP_154880245.1|2136244_2137927_-|choline-dehydrogenase
MSTHNEYDYIIIGAGSAGNVLATRLTEDADVSVLLLEAGGPDYRLDFRTQMPAALAFPLQGKRYNWAYKTDPEPFMNNRRMDCGRGKGLGGSSLINGMCYIRGNAMDYDNWAGMPGLEDWTYLDCLPYFRKAETRDIGPNDYHGGDGPLRVTTPKAGNNELFAAMVEAGVQAGYPRTDDLNGYQQEGFGPMDRTVTPKGRRSSTARGYLDLAKPRPNLTIVTHALTDRILFSGKRAVGVQWLHNDQPQRATARREVLLCGGAIASPQILQRSGVGPADLLRSLDIDLVHHLPGVGANLQDHLEMYLQYECKKPVSLAPALKLYNQPAIGAEWLFLGTGIGASNQFEAGGFIRSDAEFDWPNLQYHFLPVAINYNGSNPIKAHSFQMHVGSMRSPSRGRIHVRSKDPREDPSILFNYMSHDQDWREFRSAIRITREIFAQPALAPYSGREISPGSALQTDTQIDAFVREHAETAYHPSCSNKMGHADDPMAVVDGQGRVHGLEALRIVDASIMPQVVTGNLNAPTIMIAEKLADVIRGRAPLPRSTASYYKANGAPVRNKS
>NZ_CP040429.1|WP_059064111.1|2134173_2135850_-|long-chain-fatty-acid--CoA-ligase
MSLDRPWLQSYPKGVPAEIDVNEFHSVVSVFDASVAKYRDRPAYSSFGKTLTYGETDALVEQFAAYLLGELKLKKGDRVALMMPNCLQYPIATFGVLRAGLTVVNVNPLYTARELKHQLVDAGVTALVVVDNFGDTVEQVIADTQVKQVITTGLGDLLGAKGTIVNFVLKYVKKMVPNYHLKGAIRFKQALKLGSRHTLPKVEIDHDDVAFLQYTGGTTGVAKGAMLTNRNLIANMQQASAWISASGIEMGKEWIITALPLYHIFALTANGLVFMKFGGCNHLITNPRDMKGFVKELKSVRFTAITGVNTLFNGLLNTPGFDTVDFSSLKVTLGGGMAVQRAVAERWKKTTGVTLVEAYGLTETSPAACINPLTLAEYNGSIGLPIPSTDACIKDDNGNILALGEVGELCIRGPQVMKGYWQRPEETAKAIDADDWLHTGDMAKMDEHGFFYIVDRKKDMILVSGFNVYPNEVEDVIAMMPGVLEVAAVGVPDEKSGEVVKVVIVKKDPNLTAEMVKEHARANLTGYKHPRIVEFRKELPKTNVGKILRRELRDTPAP
>NZ_CP040429.1|WP_134832495.1|2149136_2150087_-|hypothetical-protein
MALRPACLTAAIAASLLLAPSAYAVDEAPTPVAASAVTSGASPDPATDATPVTDIAEAAPAAAAVAGPAVGDVTVAVAPALDLSSLQRVKVTSGLGVGPNGNRVGDHVLRLVMRGDTAAVTAAKVGLSALAFVTGVGDIGTSNSFSKNNVRGEDIQSVPSPAFGALPGMIREQLALYFAAHPGAIPSDERTVEASAGQWSLVYQKLSDAETPYELRHDVTIGFPLVRKLFRSASGGQGVHCQDEARVAPLQEWQADDYAKAKAASREFAEACIVRFVAELPRLFPDHGALPETAAEPELPMDTPAVTEEAAAAAQA
>NZ_CP040429.1|WP_154880251.1|2150131_2151727_-|hypothetical-protein
MAQRRFPTRTSLLTAALLAPLAATSAAQSAPPHTTPVAATATATTTDHPAPWTDRVQIQSGPAGALKRMHAPDVALRIVTPDDSEALTPKGLALLFSGNEPDYFQRNNLPGSIIEGQASPAITLMPNVAKALVGGYFRYAPDALPAQTSTLRFSADTWALVHQGNTRKDPLYRLNHSSTIEQRRADGTLAEIISCNDSDNRATLEAWQADDYARLKGAAQMITMKCIEKLVKRIAAMYPRPLAAEDVSAYADGAAPPARVRVYAALGRTTTLYTDAACREDYRDRIDVKYNNAGDKGVLGIPVTETLRSKENERFSTLSYQEYEVPGGKPLIFEARFDASSRVYCDGKLSGQFVARPGQDYEVEFEVADKICRLHIRQVHADGSMTPQQARATPTICERTRAPVRIEPRQEMQVLLFSPGEVQIQDASLSSAPQRLSDDAGSSQALQQMLQQASSTPGTRLCVVVPAADYSSVLHDAVRERVLDAPQVLPSLWEETSTVNQRRNAAADAPVDIAAAVTRCKAFPIKEFAAQ
>NZ_CP040429.1|WP_099783897.1|2151814_2152888_-|chemotaxis-response-regulator-protein-glutamate-methylesterase
MTLTGNAPCRVLIVDDSAVVRQMLTEILSSDPAIDVVGTAADPLLAREKIKRLAPDVITLDVEMPRMDGLAFLENLMRLHPLPVVMISSLTERGADTTLQALGLGAVDFVSKPKLDVARGLQGYADEIIAKVKMAARSRVRPLVRVATPKLTLDAAPAARPAATQFRTTDRLIAIGSSAGGTEALRVVLEGMPADGPAVVMTQHLPASFSTAFAERLDRHSAMAVREASDGEAVLPGHAYLPPGGKHLRIIRDGARWRCRVDDGPAVNRHKPAVDVLFRSVAQSAGGNAIGAILTGMGDDGARGLLEMRQAGAPTLVQDEATSVVWGMPGAAFKLGAAEEQVPLERIAERLLALARG
>NZ_CP040429.1|WP_025878962.1|2152884_2153481_-|chemoreceptor-glutamine-deamidase-CheD
MNASLRTDDVMRYQDARFKTIAAKLLPTQYLVVDDTTALTTTLGSCVAACLRDPVLKIGGMNHFLLPEGNAGDGAPARYGSYAMELLINDMLKRGAHRKRIEAKVFGGANVLKGFTSNPVGTRNAEFVRQYLQAEHIPILAEDLCGIHPRKIWFFADTGRVVVQRLPHAHEAEVAATESAVRARLSKAPVTGGVELFE
>NZ_CP040429.1|WP_032975462.1|2153477_2154347_-|chemotaxis-protein-CheR
MDTSPVQSPTPIVSGTREFEFADRDFRRVCDLIYQRVGIALAPAKRDMVYGRLSRRLRTLGMRSFQQYLDHLEQGDGDEWQAFTNALTTNLTAFFREPHHFDKLREELQQRNGRGPLLLWSCAASTGEEPYSMAITACEAFGTLKPPVRIVATDVDTQVLATAGRGVYNIDRVAGLDPDLRRRYFQRGSGPNEGQCRVLPALRELIEFRPLNLLAPRYDVGGPFDALFCRNVMIYFDKPTQRAILGRLVNHLADDGLLYTGHSENYLHAADLIQPCGRTLYRRAAKAGA
>NZ_CP040429.1|WP_154880253.1|2154379_2156644_-|HAMP-domain-containing-protein
MNLLHRWQHYFSNLSVRRKLNLLTLLIALGVIALSVIAARMQYLDLTDTRKSSLKTQVELSYGILDHYHRLAGTGELSEEAAKAAALQALEVMRAHNDTYYYNIYDTGYHVLMHPFRKDLVGKDMKDFRTGDGIRIYYDQIEAAKAGGGFVAYRWAKPGEKGEVEKVAYAGLFKPWNWVVSSGVYMDDVQQQALVFTAIMTLAGGVLVLIVLALSWVIGNRIARPLKQATAVAEGIAGGKLDSHIGPQPHDETGRLLEAMSRMQQQLHAVISGQREMARRHDGGELSYRIDASSFPGEYGLMVQETNVLVGSHVQTLHDVLNVVQQYAVGDLSSDIARYPGEKAAMTTTVDTVKANLGRINAEIKQLASAAAAGDFSQRGDAQRFDHDFRTMLENLNAMMAVSDDNLGKLSQLLSSIADGDLTARMHGDYQGVFARMRDDANATVSQLTQIVSQIQASASSITLSAGEIASGNSDLSRRTEQQAANLEETAASMEELTSTVRQNAEHARQANQLAIGAHGVASQGGSVVGQVVTTMSAIEASSKKIAEIISVIDGIAFQTNILALNAAVEAARAGEQGRGFAVVASEVRTLAQRSAAAAKEIKGLIDDSVGKVAEGSSLVHQAGSTMGEIVASVQRVTDIMAEISAASQEQSAGIEQVNQTVVQMDETTQQNAALVEEATAAARAMEDQAAQLADAVAIFRLDNQVAVAVTAVTAKVAPKAASPAPSRPLSTPAPIRRTHSSTVVSNDGDWQEF
>NZ_CP040429.1|WP_033831025.1|2157161_2159537_-|HAMP-domain-containing-protein
MPWINNLKLMPKLMLTFGVLLLVMLLQGIVAYRGLHSLNNVTTELAGSRMESIRMAGEMRGMLGEYRNSAYQQLIRASDDVKADARKQAVELRTSMDKSIKDYPKLVDNAQQKKLFDTFAKDWKDALASYDSVTEMLELDLPDDAIDTFVGETRTKHRKAGAALEALIAEDNRLARASRDEAASTYSASAVLTVIALLGGAALGLVLVWLFARALVGSVRGAVSVANDVAGGKLDGHIDVSRQDEVGELMQAMQRMQRDLRERTETDQAIARENLRIRTALDYSSTGVYLTDPNNTIVYSNRALQQTLAQYQDELRRDLPDFDVHASLVGKPVTVLEHRGEMDNTLLANLKQHGVARRPMQYGDAQFAQVVSTIRNEDGDTVGYVVEWRDRTQEAQVEAEVARVIAQAAAGDLSGRIDANDKEGFFLQLAQQINGLLDANSGSIEQISGLLAALSQGDLTVRMHGDYQGVFARMRDDANATAAQLSEIVTRIKQSSRAISSAAGEIASGNSDLSRRTEQQAANLEETAASMEELTSTVRQNAEHARQANQLAIGAHGVASQGGEVVGQVVTTMSAIQASSKKIAEIISVIDGIAFQTNILALNAAVEAARAGEQGRGFAVVASEVRTLAQRSAAAAKEIKGLIDDSVGKVNDGSALVHKAGATMGEIVASVQRVTDIMSEISAASQEQSAGIEQVNQTVVQMDETTQQNAALVEEATAAARAMEEQAGHLSEAVSIFVVDEAEAVVATRAPAPRASAPAAPAPAAAVPPARRSTGGRSMATELADGDWQEF
>NZ_CP040429.1|WP_025878966.1|2159635_2160019_-|hypothetical-protein
MKSLLAFVSAAVLATTASSAFAQSAEMIPPEMAPRAVGKDGMVCGKVEKARFAEGSEGQPTFLYMGGAFPRHTFSARIAGENRGKFSFPLETLEGKTVCVIGKIQRDASRAEIEVSSPSSLKLANIK
>NZ_CP040429.1|WP_025878967.1|2160156_2160648_-|chemotaxis-protein-CheW
MNDKNSSAAGADGEFLSFTLGAEHYGVDILKVQEIRGYDAVTRVPDAPDYIKGVINLRGTIVPVIDLRLKLRLEDARYDAFTVMIVLNVEDRVVGIVVDSVSDVIPLSAEQIRPTPEFGAAVDTRFISGIGTHDDRMLILLDIETLLDSADMGQTNVVEDAAA
>NZ_CP040429.1|WP_025878968.1|2161038_2161812_-|flagellar-brake-protein
MSDGHDTALPEVHAADAADDRFLVRNPRQVRQLLRSLIDQRSLINAHIDGRDRSFPTALLELDDDEDFLLLDGSPQEASNRAAEQSDHLLCFAQLERVLVRFRLHDLQRVDNEGHVAFRAPLPDELVHLQRRELYRLETPITDSPQLLLPPGEARAEALSMRVVDISGGGLAVTVPTDCAIFSLQQRYRAQLSMPDGPDLQIELVVCNLLPQRLPNGTEVKRVGMRFDDLPRGGDSAIQRYIFRIDRQRKARRNGEL

Crispr_ID: NZ_CP040429_11

• CRISPR_ID: NZ_CP040429_11
• CRISPR_location: 3345478-3345616
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_11

Consensus_repeat	Method
CGCTCCGGTAGATGCCAACCTTGGTTGGCACGCCTCTGCCGGCCAGCGGC	CRISPRCasFinder

spacers of NZ_CP040429_11

>11.1|3345528|39|NZ_CP040429|CRISPRCasFinder
CAGCACTACCGCAAGGCGTGCCGGTCAAAGCTGACCCAC

CRISPR arrays and Neighbor proteins around NZ_CP040429_11

CRISPR arrays

The CRISPR arrays of NZ_CP040429_11

>merge|NZ_CP040429|11|3345478-3345616|CRISPRCasFinder
CGCTCCGGTAGATGCCAACCTTGGTTGGCACGCCTCTGCCGGCCAGCGGCCAGCACTACCGCAAGGCGTGCCGGTCAAAGCTGACCCACCGCTCCGGTAGGTGCCAACCTTGGTTGGCACGCCTCTGCCGGCCAGCGGC

>NZ_CP040429|11|10|3345478-3345616|CRISPRCasFinder
CGCTCCGGTAGATGCCAACCTTGGTTGGCACGCCTCTGCCGGCCAGCGGC	CAGCACTACCGCAAGGCGTGCCGGTCAAAGCTGACCCAC
CGCTCCGGTAGGTGCCAACCTTGGTTGGCACGCCTCTGCCGGCCAGCGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_032976602.1|3359282_3361901_-|Fe/S-dependent-2-methylisocitrate-dehydratase-AcnD	unknown	unknown	gnl|CDD|131386
NZ_CP040429.1|WP_154880936.1|3336900_3337551_+|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|366703
NZ_CP040429.1|WP_025877044.1|3340035_3341328_-|adenylosuccinate-synthase	unknown	unknown	gnl|CDD|234904
NZ_CP040429.1|WP_025877040.1|3341867_3342731_-|protease-modulator-HflC	unknown	unknown	gnl|CDD|259803
NZ_CP040429.1|WP_025877010.1|3362010_3363168_-|2-methylcitrate-synthase	unknown	unknown	gnl|CDD|183463
NZ_CP040429.1|WP_154880941.1|3357264_3358449_-|2-methylaconitate-cis-trans-isomerase-PrpF	unknown	unknown	gnl|CDD|131387
NZ_CP040429.1|WP_025877015.1|3358483_3359188_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154880940.1|3355704_3357165_-|bifunctional-2-methylcitrate-dehydratase/aconitate-hydratase	unknown	unknown	gnl|CDD|181845
NZ_CP040429.1|WP_025877033.1|3345668_3346559_-|DnaJ-domain-containing-protein	unknown	unknown	gnl|CDD|237667
NZ_CP040429.1|WP_033831761.1|3347331_3347913_+|bacterioferritin	unknown	unknown	gnl|CDD|225104
NZ_CP040429.1|WP_154880937.1|3339234_3339891_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_032976611.1|3344016_3345012_+|YhdH/YhfP-family-quinone-oxidoreductase	unknown	unknown	gnl|CDD|176183
NZ_CP040429.1|WP_154881366.1|3337705_3339070_+|deoxyguanosinetriphosphate-triphosphohydrolase	unknown	unknown	gnl|CDD|234897
NZ_CP040429.1|WP_154880938.1|3348187_3350572_-|penicillin-binding-protein-1C	unknown	unknown	gnl|CDD|183049
NZ_CP040429.1|WP_025877042.1|3341614_3341800_-|DUF2065-family-protein	unknown	unknown	gnl|CDD|225782
NZ_CP040429.1|WP_025877032.1|3346818_3347301_+|peroxiredoxin	unknown	unknown	gnl|CDD|239311
NZ_CP040429.1|WP_025877038.1|3342727_3343864_-|FtsH-protease-activity-modulator-HflK	unknown	unknown	gnl|CDD|259802
NZ_CP040429.1|WP_154880935.1|3335930_3336896_+|L,D-transpeptidase-family-protein	unknown	unknown	gnl|CDD|341130
NZ_CP040429.1|WP_154880939.1|3350621_3355529_-|alpha-2-macroglobulin-family-protein	unknown	unknown	gnl|CDD|225248
NZ_CP040429.1|WP_005410644.1|3345100_3345472_+|response-regulator	unknown	unknown	gnl|CDD|381093

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_032976602.1|3359282_3361901_-|Fe/S-dependent-2-methylisocitrate-dehydratase-AcnD	gnl|CDD|131386	TIGR02333, 2-methyl_citrate_dehydratase_Fe-S_dependent_AcnD, 2-methylisocitrate dehydratase, Fe/S-dependent. Members of this family appear in an operon for the degradation of propionyl-CoA via 2-methylcitrate. This family is homologous to aconitases A and B and appears to act the part as 2-methylisocitrate dehydratase, the enzyme after PrpD and before PrpB. In Escherichia coli, which lacks a member of this family, 2-methylisocitrate dehydratase activity was traced to aconitase B (TIGR00117) ().	0
NZ_CP040429.1|WP_154880936.1|3336900_3337551_+|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	6.78532e-26
NZ_CP040429.1|WP_025877044.1|3340035_3341328_-|adenylosuccinate-synthase	gnl|CDD|234904	PRK01117, PRK01117, adenylosuccinate synthetase; Provisional.	0
NZ_CP040429.1|WP_025877040.1|3341867_3342731_-|protease-modulator-HflC	gnl|CDD|259803	cd03405, SPFH_HflC, High frequency of lysogenization C (HflC) family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model characterizes proteins similar to prokaryotic HflC (High frequency of lysogenization C). Although many members of the SPFH (or band 7) superfamily are lipid raft associated, prokaryote plasma membranes lack cholesterol and are unlikely to have lipid raft domains. Individual proteins of this SPFH domain superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. Escherichia coli HflC is an integral membrane protein which may localize to the plasma membrane. HflC associates with another SPFH superfamily member (HflK) to form an HflKC complex. HflKC interacts with FtsH in a large complex termed the FtsH holo-enzyme. FtsH is an AAA ATP-dependent protease which exerts progressive proteolysis against membrane-embedded and soluble substrate proteins. HflKC can modulate the activity of FtsH. HflKC plays a role in the decision between lysogenic and lytic cycle growth during lambda phage infection.	3.62526e-107
NZ_CP040429.1|WP_025877010.1|3362010_3363168_-|2-methylcitrate-synthase	gnl|CDD|183463	PRK12351, PRK12351, methylcitrate synthase; Provisional.	0
NZ_CP040429.1|WP_154880941.1|3357264_3358449_-|2-methylaconitate-cis-trans-isomerase-PrpF	gnl|CDD|131387	TIGR02334, conserved_hypothetical_protein, probable AcnD-accessory protein PrpF. The 2-methylcitrate cycle is one of at least five degradation pathways for propionate via propionyl-CoA. Degradation of propionate toward pyruvate consumes oxaloacetate and releases succinate. Oxidation of succinate back into oxaloacetate by the TCA cycle makes the 2-methylcitrate pathway a cycle. This family consists of PrpF, an incompletely characterized protein that appears to be an essential accessory protein for the Fe/S-dependent 2-methylisocitrate dehydratase AcnD (TIGR02333). This protein is related to but distinct from FldA (part of pfam04303), a putative fluorene degradation protein of Sphingomonas sp. LB126. [Energy metabolism, Fermentation].	0
NZ_CP040429.1|WP_154880940.1|3355704_3357165_-|bifunctional-2-methylcitrate-dehydratase/aconitate-hydratase	gnl|CDD|181845	PRK09425, prpD, bifunctional 2-methylcitrate dehydratase/aconitate hydratase.	0
NZ_CP040429.1|WP_025877033.1|3345668_3346559_-|DnaJ-domain-containing-protein	gnl|CDD|237667	PRK14299, PRK14299, chaperone protein DnaJ; Provisional.	4.883e-74
NZ_CP040429.1|WP_033831761.1|3347331_3347913_+|bacterioferritin	gnl|CDD|225104	COG2193, Bfr, Bacterioferritin (cytochrome b1) [Inorganic ion transport and metabolism].	2.01751e-33
NZ_CP040429.1|WP_032976611.1|3344016_3345012_+|YhdH/YhfP-family-quinone-oxidoreductase	gnl|CDD|176183	cd05280, MDR_yhdh_yhfp, Yhdh and yhfp-like putative quinone oxidoreductases. Yhdh and yhfp-like putative quinone oxidoreductases (QOR). QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR actin the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	1.34809e-164
NZ_CP040429.1|WP_154881366.1|3337705_3339070_+|deoxyguanosinetriphosphate-triphosphohydrolase	gnl|CDD|234897	PRK01096, PRK01096, deoxyguanosinetriphosphate triphosphohydrolase-like protein; Provisional.	0
NZ_CP040429.1|WP_154880938.1|3348187_3350572_-|penicillin-binding-protein-1C	gnl|CDD|183049	PRK11240, PRK11240, penicillin-binding protein 1C; Provisional.	0
NZ_CP040429.1|WP_025877042.1|3341614_3341800_-|DUF2065-family-protein	gnl|CDD|225782	COG3242, COG3242, Uncharacterized protein conserved in bacteria [Function unknown].	2.12378e-11
NZ_CP040429.1|WP_025877032.1|3346818_3347301_+|peroxiredoxin	gnl|CDD|239311	cd03013, PRX5_like, Peroxiredoxin (PRX) family, PRX5-like subfamily; members are similar to the human protein, PRX5, a homodimeric TRX peroxidase, widely expressed in tissues and found cellularly in mitochondria, peroxisomes and the cytosol. The cellular location of PRX5 suggests that it may have an important antioxidant role in organelles that are major sources of reactive oxygen species (ROS), as well as a role in the control of signal transduction. PRX5 has been shown to reduce hydrogen peroxide, alkyl hydroperoxides and peroxynitrite. As with all other PRXs, the N-terminal peroxidatic cysteine of PRX5 is oxidized into a sulfenic acid intermediate upon reaction with peroxides. Human PRX5 is able to resolve this intermediate by forming an intramolecular disulfide bond with its C-terminal cysteine (the resolving cysteine), which can then be reduced by TRX, just like an atypical 2-cys PRX. This resolving cysteine, however, is not conserved in other members of the subfamily. In such cases, it is assumed that the oxidized cysteine is directly resolved by an external small-molecule or protein reductant, typical of a 1-cys PRX. In the case of the H. influenza PRX5 hybrid, the resolving glutaredoxin domain is on the same protein chain as PRX. PRX5 homodimers show an A-type interface, similar to atypical 2-cys PRXs.	5.82689e-77
NZ_CP040429.1|WP_025877038.1|3342727_3343864_-|FtsH-protease-activity-modulator-HflK	gnl|CDD|259802	cd03404, SPFH_HflK, High frequency of lysogenization K (HflK) family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model characterizes proteins similar to prokaryotic HflK (High frequency of lysogenization K). Although many members of the SPFH (or band 7) superfamily are lipid raft associated, prokaryote plasma membranes lack cholesterol and are unlikely to have lipid raft domains. Individual proteins of this SPFH domain superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. Escherichia coli HflK is an integral membrane protein which may localize to the plasma membrane. HflK associates with another SPFH superfamily member (HflC) to form an HflKC complex. HflKC interacts with FtsH in a large complex termed the FtsH holo-enzyme. FtsH is an AAA ATP-dependent protease which exerts progressive proteolysis against membrane-embedded and soluble substrate proteins. HflKC can modulate the activity of FtsH. HflKC plays a role in the decision between lysogenic and lytic cycle growth during lambda phage infection.	1.49381e-115
NZ_CP040429.1|WP_154880935.1|3335930_3336896_+|L,D-transpeptidase-family-protein	gnl|CDD|341130	cd16913, YkuD_like, L,D-transpeptidases/carboxypeptidases similar to Bacillus YkuD. Members of the YkuD-like family of proteins are found in a range of bacteria. The best studied member Bacillus YkuD has been shown to act as an L,D-transpeptidase that gives rise to an alternative pathway for peptidoglycan cross-linking. Another member Helicobacter pylori Csd6 functions as an L,D-carboxypeptidase and regulates helical cell shape and motility. The conserved region contains a conserved histidine and cysteine, with the cysteine thought to be an active site residue.	2.27008e-26
NZ_CP040429.1|WP_154880939.1|3350621_3355529_-|alpha-2-macroglobulin-family-protein	gnl|CDD|225248	COG2373, COG2373, Large extracellular alpha-helical protein [General function prediction only].	0
NZ_CP040429.1|WP_005410644.1|3345100_3345472_+|response-regulator	gnl|CDD|381093	cd17538, REC_D1_PleD-like, first (D1) phosphoacceptor receiver (REC) domain of response regulator PleD and similar domains. PleD contains a REC domain (D1) with the phosphorylatable aspartate, a REC-like adaptor domain (D2), and the enzymatic diguanylate cyclase (DGC) domain, also called the GGDEF domain according to a conserved sequence motif, as its output domain. The GGDEF-containing PleD response regulators are global regulators of cell metabolism in some important human pathogens. This model describes D1 of PleD and similar domains. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.3106e-35

Protein sequences

>NZ_CP040429.1|WP_005410644.1|3345100_3345472_+|response-regulator
MARILIVDDSPSQLLGIQRIVEKLGHQILTATDGAAGVETAKAELPDLVLMDVVMPNLNGFQATRTLARDEATRHIPVILVTTKDQDTDRMWGMRQGAKAYITKPFSEDELSEVLERVFAGQG
>NZ_CP040429.1|WP_032976611.1|3344016_3345012_+|YhdH/YhfP-family-quinone-oxidoreductase
MAPTTPFTAFRIEKDDAGYRSGLVPLRLDDLNPGQVLIRAHWSSVNYKDALAGTGKGRILRRFPLVGGIDVAGTVVASTDPAWREGDAVLATGCGLSETRDGGYSQYVRLESSAVIAQPAGLSPREAMVLGTAGFTAALALLRLQDNRQTPELGPLAVTGASGGVGALAVDIFSRAGYAVHAISGKPEQSDFLRGIGAAEVLPRDALADTGPLQSARFGGGLDNAGGPMLASLLAQTVPYGSVVSAGLAASPTLDMTVMPFILRGVSLLGVSSANAPRALREEVWARLGDAWKPQHLDRICTAEVGLDGLPAVFDRMLAGGSLGRTVVRID
>NZ_CP040429.1|WP_025877038.1|3342727_3343864_-|FtsH-protease-activity-modulator-HflK
MAWNTPGGNKGGQGPEDNRRGPFGSRGGGNGGGWGGLPGPLKDLFDGGILRWVVAAVVLLVLFSSFQLIGEQQRGVVLRFGQFSRVLTPGPNFKLPWPIESVTKVNATEIKTFSIQVPVLTRDENIVNVSLNVQYRIDDPQQYLFGTVDANQVLEQSAQSAVREEVGRADLNAVLNNRGPLAVAAEERLQTLLRAFKTGLTVTGLTLQDARPPEEVKPAFDEVNGAQQVKERLINEAQAYAAKVVPEARGQASRARTTAEGYKQAVVSKAEGDGQRFSLLQAQYKDAPEVTRKRLWLETVQQVLSENRKVIGGDGRQLIYVPMTGDTRASTSAPAPVPNPDVVMPSLPGTTAVEASRDPGRPVGRPTGRSSGREEGSR
>NZ_CP040429.1|WP_025877040.1|3341867_3342731_-|protease-modulator-HflC
MRNSIWIAVVVAVLLGLLGSVYVVREDQTAMVLNLGKVVRSDIKPGLHFKLPVVETVRVFDRRFQVLDTAPARYFTAEQKDVSVDFFAIGYISNVGDYFRATGGDPRIANARLAPIITDSLRNQINSRTLQQLVSGDRSELIAEQLKGINEAVAGLGMQMIDLRIKQVDLPTDSQVINDVYERMRAQRKQEAAKLRAEGEEQSLTIRAQADRDSTVLIAEAERDAQRLRGEGDAEAARIYGKAGSADPSFYAFYRSLEAYRGSMTDGNGVIVLDKNDPFLQYLKNDR
>NZ_CP040429.1|WP_025877042.1|3341614_3341800_-|DUF2065-family-protein
MKDLFAAVCLVAVLEGLLLFVAPVAWKRMAERLLDLPSPALRSFGGLVLLAGLSLLWWVRH
>NZ_CP040429.1|WP_025877044.1|3340035_3341328_-|adenylosuccinate-synthase
MGQSVVVLGAQWGDEGKGKIVDLLTEEIGAVVRFQGGHNAGHTLVINGKKTVLHLIPSGILRDDALCLIGNGVVISPAALQKEIAELETSGVEVRSRLKISPAAPLIMPYHIALDQARERAAGGKAIGTTGRGIGPAYEDKVARRGIRIADLHYPKQLEELLRTALDYHNFVLTKYLNTDAVDFQKTFDEALAFGEYVQPMKSDVAGILHDLRKQGKRVLFEGAQGALLDIDHGTYPYVTSSNTTVGGALAGAGVGADAIDYVLGIAKAYATRVGGGPFPTELDDEIGQGIRDRGAEYGASTGRPRRCGWMDIVALKRAVAINGISGLCITKLDVLDGMEKLKVCIAYEYNGKRTEYAPLDAQGWEECTPVYLEFPGWTENTHGITNWDDLPPAARAYLRSLEELAGCPISIVSTGPDRDHTMVLQDPFA
>NZ_CP040429.1|WP_154880937.1|3339234_3339891_-|hypothetical-protein
MTGDVSAKGTRVLRITLWVFWGLWAVACVVLAVGAVANHLASRTQTLPLVLSPGASAEITVYRFIDDRLRLRLRYPPNAADPALDPDVLMRVDTPNEHADFRAGVRSGPAGTDVVRRLETVETAVFTAAYFGYGRGDALPRGRSWLRVTVLEVEPALAGRPAMIEVQPPLDLLKLTDLDYLWLWPFFFWKLAALLLLVPGIVLVIFTIALRRQRPRTA
>NZ_CP040429.1|WP_154881366.1|3337705_3339070_+|deoxyguanosinetriphosphate-triphosphohydrolase
MQWEKLLSSTRLGKRPAKVEEGRSPFNSDHDKVIFSGSFRRLARKTQVHPLATNDHIHNRLTHSLEVACVGRTLGMRVGHELIKGKKLPAHLTAADIGDIVQTACLAHDIGNPPFGHTGEEAIRHWFSNESEDILRNLKPNESADLKLFEGNAQGFRVLTTSEYHPYDGGMRLTYASLGAFIKYPWISLDAASGNRPKNSKYGIYRSEEDKFKEVAEATGLLKRGDNWYCRHPLAHLMEMADDFCYAILDLEDGIEMGILNWEEVFEIIQPVLDPKRLAELGNDLKDLRPGRKPPLVRGKIISAFVDAGAKAFIENENKILCGEIDDLLAKCDTPIITCVKNAKNLAKDRIFQHPRKVELEIGAYNTLSTILSVLCNAAISHVTNIKEGDYKSKRALDLIGRNTFDPRITSKNEENSHSPEYLALMRVMDFVSGMSDNYATHLARQFNGSGDVR
>NZ_CP040429.1|WP_154880936.1|3336900_3337551_+|peptidoglycan-DD-metalloendopeptidase-family-protein
MRLAQLIVLGLVMGVAAGWWLQRDGEPSDDTGARPLAVAQTSAAADSARAVPVEQATTAIAAPAPAATGDTPFGLLLPVQGITPSQLQDTFTDARSEGRVHDAIDIMAAAGTPVLAVADGHVEKLFDSERGGLTIYQFEPSGRWCYYYAHLQRYADRLAEKQTIKRGDVIGYVGSTGNANPEAPHLHFEVHVLGPEKQWWKGESINPYPLLIRKEP
>NZ_CP040429.1|WP_154880935.1|3335930_3336896_+|L,D-transpeptidase-family-protein
MPMPVCRPALLALSLLMSPAFAQTPPPAGLPAPIAEKAGPDTAAHSPLHAQVLLDRANFSPGEIDGEVGSNQRRAVSGFQAAHGLTVSGELDDATWKALQADSVGPLASYTLTAEDVAGPFVAVPKKPADQAKLKALGFSNVEESLGERFHAAPELLKALNPGVDLSKAGSRIQVPNIAPAALPKAAKLVVDKSDSTLQLLDAQGKVIAQVPVSSGSEHDPLPIGEWKILGVYPDPPFHYNPKLFWDARKGDRKATIPPGPNNPVGRVWIDLSKPHYGLHGTPVPGHVGKTESHGCVRMTNWDVLRVAAAVDTSVPVVMQE
>NZ_CP040429.1|WP_025877033.1|3345668_3346559_-|DnaJ-domain-containing-protein
MEFKDYYATLGVEPSAGEAEIKTAYRRLARKYHPDVSKEAGAEDKFKAINEAYEALRDPEKRAAYDQLRAQGYRPGEEFNVPPNYGGGGFNFEEVFGGGGPNGGFSDFFESLFARQRGGQGAGPGPGFSSHGHAPNRDTRAKLSVPLEAAYNGDSLRITVNGKQLDVRVPKGIRPGQVIRLAGQGNHGGNLLLEVEYAAHPQFEVDGRNILYTLPVTPWQAALGTSISVPTLGGAVELKIPADSDAGRKLRLRGRGLPGSPEGDQIVELEIVAPAATDDAQKKAYRNLAKAFGETI
>NZ_CP040429.1|WP_025877032.1|3346818_3347301_+|peroxiredoxin
MTIHVGDRIPEVTLKRIREGIETLDTHALFDGRKVVLFAVPGAFTPTCSARHLPGYVEKFEAFRHRGIDVYCVAVNDPFVMKAWATDQHVPDGLLMLSDGNAELTRALGLELDASSSGMGTRSRRFALYVVDGTVRAAWIEEPGQFEVSSADYVLDHLPT
>NZ_CP040429.1|WP_033831761.1|3347331_3347913_+|bacterioferritin
MSNKPAKASNTSPSAKVAGISDRQTLRERARKNIEDGAITDSYSADRKVVIKLLNDALATEYVCVLRYYRHYFMAKGMLADAVKGEFLEHAQQEQAHAGKLAERIVQLGGEPDLNPDTLTARSHAEYKEGSDLRDMVRENLVAERIAIDSYREMINFIGDSDTTTKRILEEILAQEEEHADEFADLLDGWIGE
>NZ_CP040429.1|WP_154880938.1|3348187_3350572_-|penicillin-binding-protein-1C
MKVGLLKTRLPRLRQRLQPLWPWLRWGTATLLALLLVLDFAFPPPLPRQRDTSTLVVAADGSPMRAFADAEGVWRYPASVDSVSPLYLQALLTYEDRWFWQHPGINPLAILRAGGQLLRGGRIVSGGSTLTMQVARILDPHTRTPWGKLKQMLRAVQLEVHLSKREILALYLERAPYGGTIEGVEAASWAYLGKPAAQLSHAEAALLAVLPQAPSRLRPDRHPEAAQKARNKVLARMAELGAWTPEEVEDARIENVVARSLRPPLHAALLAQRLHSAHPGQARIQSSIDIGLQRTLEERVASYFSTLPERTSAALLVVDNQTLQARAYVGTLSFGDRQRLGHVDMVQAWRSPGSTLKPFLYAMALDDGLIHSESLLVDAPQSFGSYRPGNFDMAFNGPVSAASALRLSLNVPSVDLLQRVGAARFAARLSHAGIQLRFPPGSSPNLSLILGGTGARLEDLVGAFAALNRNGIAGRVRYTDDEPMIERRLASPGASWIVREMLESNPRPGYGVGTFDVGGRPRVAWKTGTSYGYRDAWAIGSTRHYTVGVWVGRPDGTPLPGQYGAVTALPLMFEVVDSLPRQRGDAAAAPMPASVTQADICWPTGELAEGLPAALCQRRLSAYLLDGAAPPTFPEREARRWQPGRQRYLADARTGLRVSADCSAPHEEVAREIARWPALLSPWLPKATRDASQLPALSPDCRDDGREASVALHIDGLNEGATLARAPNAEHGVRLQLRALGSEQAVDWLLDGRWITQTRGAQLMQREFSDPGAHTLTALAADGAWTQVRFNVLR
>NZ_CP040429.1|WP_154880939.1|3350621_3355529_-|alpha-2-macroglobulin-family-protein
MSGPARRMRWGWTAALLAGGLLLGLAGCRNDSGQLPKASGEAIATKAEQVKEFTLLRAYPDQKSEGLSLALEFSRPLVGTQDFDKLVRFEEKVGNDDSSWTLSDDGLTLRYPFVEAGKEFSLVVSPDLLAADGSRLGKELKQKVFSGELKPVAGFASQGSVLPAKDSRGLPVVSVNVPEVDVEFLRVREKDLPTFFSQYQRGGRRGSWELSSDYERSPINKLAEPVYVNRFILGGKQNERVLTYLPTQDIKELQEPGLYFALLKRTGDYEGEFDTAFFSVSDIGLHTRAYKDKLFVHTAALKDGASLKGIDLRVLDAKGEVVLKGSTDSNGNALLDYTLDATHVLVASSGKDTSFLPFNQPALDLSEFAVAGRDNAWFDVYAWSGRDLYRPGETVRLSALLRDNDGKPIKSQPVFLRLKQPDGKTFRETRVQPGEQGYINFEQTIPAEAPTGRWQVEFRTDPASKEAIQGMTLRIEEFLPERMKLDLDSAQKTLKPGEDLRLQANGAYLYGAPADGNRFTARMAVAAEQKPVEGLPGYFFGDPTLQLPREAKDVIDTTLPANGQLREDVSLPEEATKAKAPIAVVLSGSLYETGGRTVTRTLKRVVWPAAALVGVRPLFNPDDGADSNGNARFELMRVDAAGKPQPAKGLKITLVRELRDYHWTFNDNRWDYDFTRRFENKETRTVDAGGSAVAFDFPVEWGEYRVDVFDPSTGLTSRYPFRAGWSWGDDNRGLDARPDKVKLGLDKTGYKAGDTLEVTVTPPHAGKGVLMVETDRMLYVQDIDAKPGATYKIPVTADWERHDVYITALVFRGGSAPSKITPARAVGVVHVPMDRKGRTVAVGLAAPKQMRPEQDLPVTVSAPQLAGKVAHVTVSAVDVGILNITRFPVPDAGAHFFAQRRLGIDAYDIYSRVIESFDGGSGKLKFGGDMALQALPQAKRPTARVQTVDLFSGPVQLDAKGIARIRLKVPDFNGTLRVSALVYSDDQYGKRDVETVVRAPILAEASMPRVLAPGDRSTVTLDVQNFTGKPGQFNVRVDSEGPLSLGEGTRSVQLNADAKTTLSFPLSAREGHSVAKVRVRVDGNGFKADRRYDLPVRAAWPQVLRSQVRTLDPLAAVSLDGSLMDGLMSESVNARLLVSPLPPIPFASALQGALNYPYGCAEQTTSKGYAALILDQATSSMLGADGLDAKTRRERMEGAFGRLASMQVANGNFSMWGDDGYVNPWLTPYIAEFLLDAKDGGFAVPDNVLQKALNRLSEDLLSGGNQFYGQEKRESLKFANQAYSGYVLARVNRAPLGTLRTLYDNERSKAVGGLSLVHLGVALSLQGDAKRGQAALAAGFAKSSSERPSYFGDYGSAVRDDALMIALTHENKLAKPAWDARAVDLGRGLDARRNSGWMWLSTQEQVAIARLGKALAANQKALVAGELVIGGNSEAIGERKLFGRNFDAGQLAAGVRFTPQGQPPMFASIDVAGIPRSAPAPDNSVIGVERSYFGTDGKPWSPRPLKEGEALIVRVTITADSEMPDALLTDLLPAGLEIENLNLGDAKQWADVVVDGITISDRSEAADTKHEEFRDDRYVAALKLSRGSKANVFYLVRAVTPGTYTVPPSLVEDMYRPQLRGVGRSNPTTLTVVQP
>NZ_CP040429.1|WP_154880940.1|3355704_3357165_-|bifunctional-2-methylcitrate-dehydratase/aconitate-hydratase
MSDSHTPSNARAAWDALLVDIVDYVRDTRIDSPLAFQTAHHCLLDTLGCGLEALSFPACSKLLGPLVPGISVTNGARVPGTNFVLDPVQAAFNIGATVRWLDFNDTWLAAEWGHPSDNLGGILAVADWLGRNAAALRRPPPTVHDVLLAMIKAHEIQGVLALRNSFNRVGLDHVLLVKVATTAVVAQMLGLDRERMLNAVSLAWVDGQALRTYRHAPNTGSRKSWAAGDATSRGVRLALMAATGEMGYPSVLSAPTWGFEAVSMHGQALTLGRPFGSYVMENVLFKISFPAEFHGQTAVEAAIILHQQLRAQGRTAEDIEHIAIRTQEACIRIIDKQGPLHNPADRDHCVQYMVAIALLHGRLVAEDYEDDMAADPRIDALRAKMTCHEDPQLSADYLDPDKRSIANGLTVRFNDGSALPEMLVEYPLGHARRRAEGIPLLMDKFRRHLAHRFPTAQQQRILAASLDPVALAAMPVTDYVDLYLPG
>NZ_CP040429.1|WP_154880941.1|3357264_3358449_-|2-methylaconitate-cis-trans-isomerase-PrpF
MTFLPQLRIPATYMRGGTSKGVFFRLQDLPEAAQVPGAARDALLMRVIGSPDPYGKQTDGMGGATSSTSKCVIISTASVPDHDVDYLYGQVSIDTAFVDWSGNCGNLSTAVGPFAIANGLIDPARVPRDGLCTVRIWQANIGKTIIAHVPMRDGQVQEIGDFELDGVTFPAAEIQLEFLDPSDDGDAGAMFPTGNLIDTLDVPGVGSFEVTMITAGIPTIFLNAADLGYTGTELQPAINEDKAALERFEKIRAYGALRMGLIQKLEDAATRQHTPKVAFVAPAQDYVSSSGKAIPAADIDLHARALSMGKLHHAMMGTAAVAIGTAAAIPGTLVNRAAGGGEREAVTFAHPSGTLRVGAQAALVDGQWTVSKAIMSRSARVLMEGKVRVPADTP
>NZ_CP040429.1|WP_025877015.1|3358483_3359188_-|hypothetical-protein
MGTAFYNIAGTVNTAFILLSLLGVGAQFRLVRNRRERADATDSATAVLSLNQFTVSFLAYLSFFIYGYSVTPFNHFIVWPRLLASVLVMAILVEIWRDRRSRSATTSLLTAALLLICALAGLAWGDRHVDEGRVVASAVIVVITALLAQGYAHQILLILRNGHTGAVSLRMSQLILLMDLSTIVFASAMGLRLGWPLLLLAVVSGSTKLAILYLFRWQRSAQADSRRRRLALQS
>NZ_CP040429.1|WP_032976602.1|3359282_3361901_-|Fe/S-dependent-2-methylisocitrate-dehydratase-AcnD
MNTDYRKSLPGASLDYFDARAAVDAIQPGAYATLPYVSRVLAENLVRRCDPATLTDSLKQLIERRRDLDFPWFPARVVCHDILGQTALVDLAGLRDAIADKGGDPAKVNPVVPVQLIVDHSLAVECGGFDPQAFEKNRAIEDRRNEDRFHFIDWTKLAFENVDVIPPGNGIMHQINLEKMSPVIYVQDGVAFPDTCVGTDSHTPHVDALGVIAIGVGGLEAENVMLGRASWMRLPDIIGVELTGRPQPDITATDVVLALTEFLRKERVVGAWLEFFGEGAAALTIGDRATISNMCPEYGATAAMFYIDGQTIDYLRLTGREEKQVALVESYARSTGLWADDLATAEYERVLHFDLSTVVRNMAGPSNPHRRLPVSELVERGIADAAKLEAGKAEQAQGLMPDGAVIIAAITSCTNTSNPRNVIAAGLLARKANERGLLRKPWVKSSLAPGSKAVQLYLEEAGLLPDLEKLGFGIVAFACTTCNGMSGALDPKIQQEIIDRDLYATAVLSGNRNFDGRIHPYAKQAFLASPPLVIAYAIAGTIRFDIEKDVLGVDTDGNEVRLKDIWPSDAEIDAVVKAAVKPEQFRSVYNPMFNVRVEHGAAVSPLYDWRPQSTYIRRPPYWEGALAGERSLAGMRALAVLPDNITTDHLSPSNAILASSAAGEYLAKMGLPEEDFNSYATHRGDHLTAQRATFANPKLFNEMVRNEDGSVKQGSLARVEPEGKVMRMWEAIETYMERKQPLIIIAGADYGQGSSRDWAAKGVRLAGVEAIVAEGFERIHRTNLIGMGVLPLEFKPGTTRLTLGIDGTETFDVIGERTPRAELRVVIHRRDGQDVIVPVTCRLDSDEEVAIYEAGGVLQRFAQDFLEGAKVA
>NZ_CP040429.1|WP_025877010.1|3362010_3363168_-|2-methylcitrate-synthase
MNDTTATPTFKPKKSVALSGTAAGNTALCSVGRSGNDLHYRGYDILDLANTSEFEEIAYLLVHGKLPTRAELVSYKAKLKSLRGIPAAVKAALEELPPSAHPMDVMRTGVSVLGCVAPEKDDHNHPGARDIADKLMACLGSMLLYWYHWSHNGRAIDVETDDDSIGGHFLHLLHGEKPQDSWVKAMHTSLILYAEHEFNASTFACRVIAGTGSDMYSAICGGIGALRGPKHGGANEVAFEVQKRYDNPDEAEEDIKARVERKEVVIGFGHPVYTVSDPRNKVIKDVARELSEEQSSMKMYDIAERLETVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVIARTAGWSAHIVEQRIDGKIIRPSANYIGPEDRDFVAIDKRS

Crispr_ID: NZ_CP040429_12

• CRISPR_ID: NZ_CP040429_12
• CRISPR_location: 3698191-3698301
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_12

Consensus_repeat	Method
GTTCATCCACGCATGGCGTGGATCTAC	CRISPRCasFinder

spacers of NZ_CP040429_12

>12.1|3698218|57|NZ_CP040429|CRISPRCasFinder
TGGAAGTGTCTGGAAGTTCATCCACGCATGGCGTGGATCTGCTGGAAGTGTCTGGAA

CRISPR arrays and Neighbor proteins around NZ_CP040429_12

CRISPR arrays

The CRISPR arrays of NZ_CP040429_12

>merge|NZ_CP040429|12|3698191-3698301|CRISPRCasFinder
GTTCATCCACGCATGGCGTGGATCTACTGGAAGTGTCTGGAAGTTCATCCACGCATGGCGTGGATCTGCTGGAAGTGTCTGGAAGTTCATCCACGCATGGCGTGGATCTAC

>NZ_CP040429|12|11|3698191-3698301|CRISPRCasFinder
GTTCATCCACGCATGGCGTGGATCTAC	TGGAAGTGTCTGGAAGTTCATCCACGCATGGCGTGGATCTGCTGGAAGTGTCTGGAA
GTTCATCCACGCATGGCGTGGATCTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_154881027.1|3702388_3704713_-|transcriptional-regulator	unknown	unknown	gnl|CDD|226233
NZ_CP040429.1|WP_025874158.1|3701373_3702273_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197666
NZ_CP040429.1|WP_154881025.1|3693526_3694468_-|DUF4880-domain-containing-protein	unknown	unknown	gnl|CDD|226235
NZ_CP040429.1|WP_032976755.1|3695157_3695634_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_032976761.1|3704972_3705644_-|ion-channel	unknown	unknown	gnl|CDD|369572
NZ_CP040429.1|WP_059065039.1|3713634_3715371_+|acetolactate-synthase-2-catalytic-subunit	unknown	unknown	gnl|CDD|181601
NZ_CP040429.1|WP_154881024.1|3690442_3693358_-|TonB-dependent-receptor-plug-domain-containing-protein	unknown	unknown	gnl|CDD|273807
NZ_CP040429.1|WP_032976752.1|3690043_3690301_+|DUF2789-domain-containing-protein	unknown	unknown	gnl|CDD|378527
NZ_CP040429.1|WP_025874164.1|3694571_3695072_-|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP040429.1|WP_154881028.1|3705745_3707590_-|phosphomethylpyrimidine-synthase-ThiC	unknown	unknown	gnl|CDD|236451
NZ_CP040429.1|WP_025874150.1|3715354_3715606_+|acetolactate-synthase	unknown	unknown	gnl|CDD|226486
NZ_CP040429.1|WP_154881030.1|3710159_3711878_-|gamma-glutamyltransferase	unknown	unknown	gnl|CDD|223482
NZ_CP040429.1|WP_025874152.1|3712622_3713597_+|ketol-acid-reductoisomerase	unknown	unknown	gnl|CDD|235491
NZ_CP040429.1|WP_005410935.1|3696307_3696844_+|inorganic-diphosphatase	unknown	unknown	gnl|CDD|179262
NZ_CP040429.1|WP_080149883.1|3698435_3701303_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP040429.1|WP_154881029.1|3708032_3709610_+|BCCT-family-transporter	unknown	unknown	gnl|CDD|376718
NZ_CP040429.1|WP_025874168.1|3689348_3689936_-|heme-oxygenase	unknown	unknown	gnl|CDD|225770
NZ_CP040429.1|WP_080149887.1|3688849_3689317_-|DUF454-domain-containing-protein	unknown	unknown	gnl|CDD|377291
NZ_CP040429.1|WP_025874160.1|3696995_3698117_+|HDOD-domain-containing-protein	unknown	unknown	gnl|CDD|370050
NZ_CP040429.1|WP_154881026.1|3695633_3696125_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_154881027.1|3702388_3704713_-|transcriptional-regulator	gnl|CDD|226233	COG3710, CadC, DNA-binding winged-HTH domains [Transcription].	6.06131e-21
NZ_CP040429.1|WP_025874158.1|3701373_3702273_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	1.9483e-17
NZ_CP040429.1|WP_154881025.1|3693526_3694468_-|DUF4880-domain-containing-protein	gnl|CDD|226235	COG3712, FecR, periplasmic ferric-dicitrate binding protein FecR, regulates iron transport through sigma-19 [Inorganic ion transport and metabolism, Signal transduction mechanisms].	6.67325e-46
NZ_CP040429.1|WP_032976761.1|3704972_3705644_-|ion-channel	gnl|CDD|369572	pfam07885, Ion_trans_2, Ion channel. This family includes the two membrane helix type ion channels found in bacteria.	0.000899561
NZ_CP040429.1|WP_059065039.1|3713634_3715371_+|acetolactate-synthase-2-catalytic-subunit	gnl|CDD|181601	PRK08978, PRK08978, acetolactate synthase 2 catalytic subunit; Reviewed.	0
NZ_CP040429.1|WP_154881024.1|3690442_3693358_-|TonB-dependent-receptor-plug-domain-containing-protein	gnl|CDD|273807	TIGR01785, Heme/hemopexin_utilization_protein_C, TonB-dependent heme/hemoglobin receptor family protein. This model represents the TonB-dependent outer membrane heme/hemoglobin receptor/transporter found in bacteria which live in contact with animals (which contain hemoglobin or other heme-bearing globins) or legumes (which contain leghemoglobin). Some species having hits to this model such as Nostoc, Caulobacter and Chlorobium do not have an obvious source of hemoglobin-like proteins in their biological niche and so the possibility exists that they act on some other substance. [Transport and binding proteins, Cations and iron carrying compounds, Transport and binding proteins, Porins].	3.46583e-37
NZ_CP040429.1|WP_032976752.1|3690043_3690301_+|DUF2789-domain-containing-protein	gnl|CDD|378527	pfam10982, DUF2789, Protein of unknown function (DUF2789). This bacterial family of proteins has no known function.	1.94189e-30
NZ_CP040429.1|WP_025874164.1|3694571_3695072_-|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	2.08498e-27
NZ_CP040429.1|WP_154881028.1|3705745_3707590_-|phosphomethylpyrimidine-synthase-ThiC	gnl|CDD|236451	PRK09284, PRK09284, thiamine biosynthesis protein ThiC; Provisional.	0
NZ_CP040429.1|WP_025874150.1|3715354_3715606_+|acetolactate-synthase	gnl|CDD|226486	COG3978, COG3978, Acetolactate synthase (isozyme II), small (regulatory) subunit [Function unknown].	4.97791e-23
NZ_CP040429.1|WP_154881030.1|3710159_3711878_-|gamma-glutamyltransferase	gnl|CDD|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP040429.1|WP_025874152.1|3712622_3713597_+|ketol-acid-reductoisomerase	gnl|CDD|235491	PRK05479, PRK05479, ketol-acid reductoisomerase; Provisional.	0
NZ_CP040429.1|WP_005410935.1|3696307_3696844_+|inorganic-diphosphatase	gnl|CDD|179262	PRK01250, PRK01250, inorganic diphosphatase.	5.57266e-115
NZ_CP040429.1|WP_080149883.1|3698435_3701303_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	6.63971e-27
NZ_CP040429.1|WP_154881029.1|3708032_3709610_+|BCCT-family-transporter	gnl|CDD|376718	pfam02028, BCCT, BCCT, betaine/carnitine/choline family transporter.	0
NZ_CP040429.1|WP_025874168.1|3689348_3689936_-|heme-oxygenase	gnl|CDD|225770	COG3230, HemO, Heme oxygenase [Inorganic ion transport and metabolism].	2.92359e-52
NZ_CP040429.1|WP_080149887.1|3688849_3689317_-|DUF454-domain-containing-protein	gnl|CDD|377291	pfam04304, DUF454, Protein of unknown function (DUF454). Predicted membrane protein.	1.32506e-42
NZ_CP040429.1|WP_025874160.1|3696995_3698117_+|HDOD-domain-containing-protein	gnl|CDD|370050	pfam08668, HDOD, HDOD domain.	3.68075e-35

Protein sequences

>NZ_CP040429.1|WP_025874160.1|3696995_3698117_+|HDOD-domain-containing-protein
MRILLVGDTASLPAELTEFIADLGEDWQPLTATDGHAAMTAVATQGVDAVIVCPQLPDLNATTLLGQIRTLRPETIRIALVDAQHGNRPPPARLIGVAHRFLPLPLAPEVLLEALTSLEELREVLDSPRLRDAIGRIEKLPSPPHLYLSLTQALEHDDDADSADVAKLVAADPAIAAKVLQLSNSAFFSQGRTIADLRTAVTRLGLATLRDLVLASEVFSAPTLSGAERNSLQQRALMASRLAARLLPDSSAELGATAALLADIGLLLPGVRNERSEPEPADDDRPGHAEAGAYLLGLWGLPMPIIEAVAFHLQPQRANTRSFWVTGAVHVALALVNGDPVDEEYLQRAGVLNKLPQWREHANSLMGLVPSEA
>NZ_CP040429.1|WP_005410935.1|3696307_3696844_+|inorganic-diphosphatase
MGLELVSPGKNPPEEINVIIEIPKDSEPVKYEVDKETGAIFVDRILSTPMRYPCNYGYVPSTLCGDGDPADVLVVLPLPLVPGSVVRCRPVGVLKMSDEAGSDEKILAVPVSKIFSGYAHVEDIAQVSSHWLERIGHFFEHYKDLEKGKWVKLDGWGGAAEAKQILIEAHQRHLDSKA
>NZ_CP040429.1|WP_154881026.1|3695633_3696125_-|hypothetical-protein
MNWNRWRCGVLLLLAPLAALARGTHVDLIHYPTREAGWDRAYALEGALAQAFDRVCADTFCEGDYSNYRVMEFRCAVLAHRGTVQRCVWVLAASELVVQGDTGQVQVDNGRWTCPVEMRPGVPVEAFFAALEASDGLMAPLPGLDHGLFDGLADCLRAQGRDA
>NZ_CP040429.1|WP_032976755.1|3695157_3695634_-|hypothetical-protein
MRTFPARWLLCGLMVVGAAQAAPAFVDARDYPDPATGRERFLAAERMLVRGFDDVCGDTFCEGQYYNLWAMRLRCSVERATGVVGSCIWTFAGSDTWVRKEGRIDVDLGSYACVLPLASGTRLEQLLQVWQVGSGDEAIHAPLPGTTTSVYGGLTDCL
>NZ_CP040429.1|WP_025874164.1|3694571_3695072_-|RNA-polymerase-sigma-factor
MSSNALTLTELLIRERPALLRRVQRILGGDSGAEDVIQAVWFKARGVDSSQGIDNPRAYLYRLAINLATDHGRESTRRNRLLAEHYLWQEDEQISTEEQVMAQDELQRVLDAAGHLPEPTRTIFHLNRLQGLTQADIARRLGVSVTTVENHVRTALQRLAWARSGR
>NZ_CP040429.1|WP_154881025.1|3693526_3694468_-|DUF4880-domain-containing-protein
MSPPPTPRSTADDAVAEQARDWIVCLASGDISDARMDAFEQWLAQPANRRSFEHERMLWRSVGPRPAAIERRQAARRPRRLRWAMATAAALAVLVAWPDAWLRLQADHRSGHRVQDVHLPDGSRAVLDADSAIAVHFDDQRRRVELLRGRAWFDVAPDAQRRFSVAAGNGVVEDISTAFTVAHVAAGVETEVGQGRVRVASPVDGGWTYLQVGQRASYGEHRGVQRLADVAADGVGAWRQGELLLEQASVADAVHAVGRYRAGPTFVRGDLSTIPAVSAALLVDHPEQALDALAATAGLQVTRLPLGVAIVYR
>NZ_CP040429.1|WP_154881024.1|3690442_3693358_-|TonB-dependent-receptor-plug-domain-containing-protein
MYEFRRPGRAPRPSRLCIALLAAGLATAAPAVMAQSSSAAPAAAQHFDIPDQPLDDALRAYMRQSGVQVVYPSTLAKGVISQPVSGTLSADEALARLLRGSGLSVRRVSADAVTLEVAAAGQTGGVIVTDTLSVAGDRVQGGAVSDEARLLDSYRSVGSTTTIGRVALERFRGTSNGDIVKGVAGVTAGDPRVGNGFDVNIRGIQGQSRVPVIIDGGQSSMDTYRGYAGQSQRTYLDPDLISRLTITKGPSLQANASGGIGGVVEMETLNVDDVLREGRDVGVRVRGGLANGSANNLPGYEAAPRSDRSATGSQFFNVAAAGHWDRFDLVAAYAYRDNGNYFSGKHGYDDFPQTRRTLAPLNPPRTEVFNTSSRSKSTLLKGTWRIDDAQTLEAGYRRYEGTAGEIMASQIIRVDRDRVPQWDPGHVDMDSYSLRYRFNPDSELIDLRVNAWYTDADSVMYNSLTGITPWYFDRRTEWYDAPSFSGNPGYKDAYRNPLRQKRFGLDASNTSVFDGSAGRFTLDYGLSYSDEDIAPGSSGPIMHDDLVNNRFLRNAERKEYSAVASLKWAPDEHWEMLLGGRWNRVDVHDRNRLATPDGYEVQGQYRYTELLNGNPKLPSWRAKRIALLNWYPDANGNFTQESLLASPYKKGTVGDIGGWNFHDADAAEDLKVPVSWTWSQPIRRRDSAFSPTASVAFRFSEDSMVYLKYAEGTKLPSLFETTLGLFTAAKPVDELKPERAHSWELGASTIQHDLFTAGDRLALKLAYFDTRIDDLITRDYRTLSAGLIRNVDRFKVSGMEFQSSYDSGKVFADLSAHYYFKAKTCAPDIAAERRAYGVQRRIEELVGTPDCVDGGFEGSYSNTQNPPRYMVNLTLGSRLFDERLTLGTRVVHNAGPISKLDKEWNVGLSAIQQLYRPTTLVDLFASWSFNDQLSVEANVDNVTDRYYLDPLALGVMPAPGRTARLAFTWRY
>NZ_CP040429.1|WP_032976752.1|3690043_3690301_+|DUF2789-domain-containing-protein
MITTEPRMTNLFLQLGLDASAEGIARFIADHQLAAGVEVADAPYWNEAQRQFLAESLQADAAWTTVVDELNEALHEAAVKAATGL
>NZ_CP040429.1|WP_025874168.1|3689348_3689936_-|heme-oxygenase
MTVQTSLEDSRSVRLKAATRDSHGALDKRIMAGDIFADRRNFARFLRVQYRFHRSIDALYASPALDALLPDLAERRRLQQVRCDLQDLEQALPGEDIAALRDDLPLPTALGWLYVAEGSNLGGTVLYKMAAALGLDRSFGARHLAAHPDGAARHWREFTAALDAVVLSPAQEQEVIDAADAAFRSVHGHVEVEFS
>NZ_CP040429.1|WP_080149887.1|3688849_3689317_-|DUF454-domain-containing-protein
MRWLWFALGWLMVALGVIGALLPVMPTTIFLILAVACFARSSPRFEQRLLSHPRYGPSLRLWREQGAVSRKGKAFASAGMAVGFAMFCWGAHPSWRLLLGVGLFFAVSAGYVLSRPAPRFDPAPLVGVDDATDPRAARRRTTSTDSNGTSDDAAC
>NZ_CP040429.1|WP_080149883.1|3698435_3701303_-|TonB-dependent-receptor
MRLGLLPAGIALALAPSFASAQDAAAGGTTDLDRISVTGSRIRQASMETAQPVIALQRADIEKQGFTSVADIVQNLSATGSPAISRADALSSGEEVGGQYVDLRNLGPERTLVLLDGKRMGTSTGGYTDLASIPTSVVERIEVLTDGASAIYGSDAIAGVVNIITRKNFDGLEASVYGGQYGQGDGQKQVYNFVYGQTGERGSITFGAEYSKEDEVQAKDRSFSRYPNGRFHPFPTDDDANGWSPASNQGVLIDDMGTPKDANDDIWYTRANTGAGNGMGDFREFGTADYTNASQEMWLQNKLTRRSVFANGNYDLTDNIRATANVLYTKRTATSQIAGYPYQSEVYGTPLSADSIYNPLGKDANFIRRTSEFPRQTESEQETFRFSAGLEGSFEFADKFWDWDVGYVYNQNKGVKTGTGNLFIPNVQNAVGPSFMDGDVARCGTPGKVIAGCTPWNPLAPYGSTGNGSLADPALQAYLFLPSHDTYTNTTKAYSANISGSLFTLPAGDLAIAAGYEHRQESGEYNPDALLQSGLSTDLAGAPTKGSYKLDEFYVELNVPVLADMPFAKELSLDMAGRYSDYNTFGDTINSKFGLKWKPIDDLLVRATYSTGFRAPNIANMYGGTSQTFDAYTDPCDSSFGSASRNPSVAAACGARGVPANFRQITSGGAQSTGPGTQSYSAFESGSNPELQPETSKTWTAGLVYSPNFVQGLDVSLDWWKIRINNVIAAESVTSILNQCYVLGVASACDRFSRGTEGRTVNQVVDVTRTLINGGYQETAGYDLGIKYRLPEFSFGKIVVDWKTTYVDYLEYKRDNEAETPVEQHTSWATGDWGANFRVRSNLNVDWSLGNLGVNWAVRYYSSMKEPCSYDTECNLPDFNSAYTLGQPTRKVGSNTFHDVQVRYTLPWQATVSVGANNVFNHEGPVMYSQPNSSFSYYGGFDIGRYYYMKYTQRF
>NZ_CP040429.1|WP_025874158.1|3701373_3702273_-|helix-turn-helix-transcriptional-regulator
MRQLSLADRGQTVSLDKAIDDVAPTCMGVARLGSLQTAGTSFSVWMQVRGTSWVEAKEGRFRLRQGEWIAFEKESRPLVQAGRNGLCVGMNLNVEALRVLTEMADCGLYAGRGQMNRADARVALRLWRDALASGQPAQALRPLLLHLAGLQRSLADNVQRCPGRSRSRKRQVFGRMQRARLYLEGNSHRVVRIGELAELTNFSSWYLSKTFQSLYEESPQSLSARLRLERAADLLRDTDMMVGEVAAASGFDNCCSFARAFRARYGQSASRFRENDGQLPPHSAKSPVVSRKYSAATQS
>NZ_CP040429.1|WP_154881027.1|3702388_3704713_-|transcriptional-regulator
MINSEIQSPESDRVRVGECIVTLSSREVEVAGARRTRRLTPKSLGVLRVLMRQPGRVVTRDELFAEVWPDTLPTNDVLTQAVTQLRKAFSVDDDNGQAYIETIAKTGYRLLVPVQPLADHETDAIAVAEDSTASQPPAPDAVAAAGVPVVERGSRRWRRLRRRLLLALGVVMLLALVVLSVLLLRRPAPVNSPVDAAVENGTRVIGSPERPYRLITATAGFETYPTLSPDGSQVAYEGANDDGAGGNAIKVQTSGNAPARQLLSPPAGASDRFPNWSPDGREIAFARFGADASCQVLIASATGGAVRQATRCDGTELLSFDWTPDGRGLVFGSMVGRYAHRGIRVLDLATGQWRALEYAVDEDDFDYAPRYSPDGRWLVFVRNPQLGDLWRMPASGGTPEQLTTESAELRGWAWLGDGRHIVFGRRVDSEARLYYLDVERRTLRDAGLDDAQWPAVSRRGDMLAFVHRRAQFGVFRMPAQGGAGERLFASSGRDGQPMVAPDGRQLVFSSDRSGSFALWWADMQRPESLRPIEGLKPEARQAPDWSADSRHLLVVGRDEHGEAVVYEIAPRDEQLHRLPVPAEQPLQALYGADAEQLLVVERDADQHTRLSLFDRSAQPWRRLASLEGVSQARFDRSTGRVLFTRLAAGGLWSVDAALTPASVQQVSEDRPSRWRYRTWTVAGNGSIDYLGSSASCGTTLVRIQSGREEAERCLDAQRLSAGNGLSASADGNSLYLALAISDGADIGVMRLPEQPPALFPAFSKLLILNEKGPS
>NZ_CP040429.1|WP_032976761.1|3704972_3705644_-|ion-channel
MPIAVTTRWLAIARRHPSAWLLGAQLLSVLLYPALDETAAGRAAVGVFGMAVLGLALWVVQRSPLGTWLALVLAIPAVVFSLSAALLDRPALGITAQLLESLLYFYTAGALIAYMLQDHKVTRDELFAAGATFTLLAWAFAFTFAVCQQWYPGSFQGASGGAQRTWMELLYLSFSLLSGVGLSDVVPLHPQARALVMLEQFSGVMYVALVVSRLVGLTMLKRF
>NZ_CP040429.1|WP_154881028.1|3705745_3707590_-|phosphomethylpyrimidine-synthase-ThiC
MNAQLSALQQQAQQLSESVTRPIPGSRKIHVPGSRPDLQVPMREIALTRTPTVFGGEDNAPVTVYDTSGPYTDPDVRIDLSAGLPALRRGWVEERNDTEQLDGLSSSFGRAREHDPKLDPVRFPARSLPRRARAGANVTQMHYARRGIITPEMEFVAIRENQRLEAIRDAALLQQHPGEAFGASIQQIITPEFVREEIARGRAVLPNNINHPESEPMIIGRNFLTKINANIGNSAVSSGIAEEVEKLVWAIRWGGDTVMDLSTGKHIHETREWIIRNSPVAIGTVPIYQALEKVDGRAEALTWEIFRDTLIEQAEQGVDYFTIHAGVLLRYVPLTARRVTGIVSRGGSIMAKWCLAHHKENFLYTHFEDICEIMKAYDVTFSLGDGLRPGCIADANDAAQFGELETLGELTKIAWKHDVQTMIEGPGHVPMQLIKENMDKQLRECGEAPFYTLGPLTTDIAPGYDHITSAIGAAMIGWFGTAMLCYVTPKEHLGLPNRQDVRDGIMAYRIAAHAADLAKGHPGAQVRDNALSKARFEFRWEDQFHLGLDPEKAKEFHDETLPKDAHKLAHFCSMCGPHFCSMKITQDVREYAEKGMQEKSEQFRAAGAEVYQQG
>NZ_CP040429.1|WP_154881029.1|3708032_3709610_+|BCCT-family-transporter
MVFRISIALVLALVLLAGLAPGPFNTVVQAALADVIRSVGWLYLLVVFLALVFLMYLACGRFGNLRIGGEDAEPEFSRASWMSMLFAAGMGIGLVFWGAAEPISHFTKPPEGIAPQSMDAARASMRYAFFHWGLHPWAIYALIGLAMAWFQFNRNGRGLVSDMLQPIIGRHHRGWIGRVVNIAAVVATAIGVATTLGFGTIQIAAGVERVFGLQATVPVQMTIIAIAFVLYMASTASGVERGVKWLSNFNLALAALLAATVLVLGPTGFIFDTFTTTLGSYLNQLVTMSLRMSPFSGSTWVADWTIFYWAWWISWAPFVGSFIARISRGRSVREFVIGVVLAPTLLGFFWFAVFGGTALWAQIFGHADLVQALGNGYETVLFTLFDSLPASLMLSAVALVLLMIFFVTSADSAVLVLASMSTDEAGDPPLKRKLAWGIAVALIAAALLLAGGLDALQGMITIAALPFALLMVLVMVSLYRVLDQEYTRERRQAQRQRRMIDAWIAREMAAQEETQAEAARAQDQD
>NZ_CP040429.1|WP_154881030.1|3710159_3711878_-|gamma-glutamyltransferase
MSRHLARSLLAAAVLAAVPMLSQAADRITGHTFATRSEVIAPHAMAATSQPLATQIALDVMKAGGSAVDAAIAANAALGLMEPTGNGVGGDLFAIVWDPKTQKLYGYNGSGRSPKSLTLAEFQRRGLKEIPATGPLPVSVPGAVDGWFALHERFGRKPMADNLAPAIRYARDGHPVAEVIAYYWDRSVPKLSQYPGFKEQFTIDGHAPRKGEMWKNPNLADTLQKIADGGRDAFYKGDIAHTIGDYFKKNGGYLSYQDMADHHGEWVEPVSSNYRGYDVWELPPNSQGIAALQILNVLEGYDFSKIPFGSPEHVHLFVEAKKLAFADRARFYADMAFQPAPVQKLISKEYAAQRRALISMDKALKEVQPGTPKQLEEGDTIYMTVADADGMMVSLIQSNYRGMGSGMAPPGLGFILQDRGEMFVLQKNHPNGYAPGKRPFQTIIPAFITKGGKPYASFGVMGGAMQPQGHAQIVMNLVDFGMNLQEAGDAPRIQHEGSTEPTGQATAMTDGGEVNLETGFPYETVRALMRKGHRVVFADGPYGGYQAILRDPETGVYYGASESRKDGQAAGY
>NZ_CP040429.1|WP_025874152.1|3712622_3713597_+|ketol-acid-reductoisomerase
MSTNELPQTKIAVIGYGSQGRAHALNLRESGFDVVVGLRPGGPTEVKAQADGFTVKAPADAVKDADLVAVLTPDMVQKKLYEDVLASNMKQGAVLLFAHGLNVHFDMIKPREDLDVVLVAPKGPGALVRREYEIGRGVPCIWAVYQDKSGKAAEYALAYAAGLGGARANLIQTTFKEETETDLFGEQAVLCGGASALVQAGFETLVEAGYQPEIAYYEVLHELKLIVDLFYEGGISRMLEFISETAQYGDYVSGPRVIDAGTKARMKEVLKDIQDGTFTKNWVAEYEAGLPNYNKFKQADLEHPIEKVGKELRAKMVWLQGQAA
>NZ_CP040429.1|WP_059065039.1|3713634_3715371_+|acetolactate-synthase-2-catalytic-subunit
MNSPTHRSAPPNGARWLTQALEAEGVRTLFGYPGGTIMPFYDALVDSSLKHILVRHEQGAALAANGFARASGQVGVCVATSGPGASNLVTGIADAMLDSVPMVCITGQVATPLLGTDAFQELDVFGLTMPIVKHSWLVRSVDDLPRVVADAFRIAREGRPGPVLIDLPKDVQLADASHLPAHVPANVEPPPAPADAAIAEAIAALAAAEKPVVYAGGGIALGDAVQDLREFVEASAIPTVMTLRGLGALPPQHPQSLGMLGMHGTRAANMAVQESDLLLVLGARFDDRATGKLAEFAPFARVVHIDADAYEISKLRSADVAVPGNVGHAIRALRAAFPSPKAHQDAWRKRCAQHRDRFAARYDAPGQHIYAPALLKRLSELAPADTVVACDVGQHQMWVAQHCRFTHPRNHLTSGALGTMGFGLPAAMGAQFACPERTVVLVSGDGSFMMNVQELATIARCRLPVKIILLDNSSLGMVRQWQELFFAERYSEIDLSDNPDFVALAKVFGIAATRIDARDDVEGGLAALLAEPGPALLHVAIDARANVWPLVPPNTANSTMLESNPAHARQEIPNAIPA
>NZ_CP040429.1|WP_025874150.1|3715354_3715606_+|acetolactate-synthase
MQYRLDLVLQPAEGALLRVIGMAERRGFAPRAITGAPVAADDGRWHLQLVVDSQRPPETLCRQMEKIYDCVSVQMTALEGASA

Crispr_ID: NZ_CP040429_13

• CRISPR_ID: NZ_CP040429_13
• CRISPR_location: 3872002-3872113
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP040429_13

Consensus_repeat	Method
TGCCGGCCAGCGGCCGGCACTAGCGGGG	CRISPRCasFinder

spacers of NZ_CP040429_13

>13.1|3872030|56|NZ_CP040429|CRISPRCasFinder
AGGGCTGCGTCGTCGAAGGCGCGAGGCCCGACGGGCTCGTCGCAGACGAGGACGGC

CRISPR arrays and Neighbor proteins around NZ_CP040429_13

CRISPR arrays

The CRISPR arrays of NZ_CP040429_13

>merge|NZ_CP040429|13|3872002-3872113|CRISPRCasFinder
TGCCGGCCAGCGGCCGGCACTAGCGGGGAGGGCTGCGTCGTCGAAGGCGCGAGGCCCGACGGGCTCGTCGCAGACGAGGACGGCTGCCGGCCAGCGGCCGGCACTACCGGGG

>NZ_CP040429|13|12|3872002-3872113|CRISPRCasFinder
TGCCGGCCAGCGGCCGGCACTAGCGGGG	AGGGCTGCGTCGTCGAAGGCGCGAGGCCCGACGGGCTCGTCGCAGACGAGGACGGC
TGCCGGCCAGCGGCCGGCACTACCGGGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP040429.1|WP_099785438.1|3878059_3878689_-|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223620
NZ_CP040429.1|WP_025877271.1|3883259_3883520_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154881078.1|3875778_3877749_-|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl|CDD|224287
NZ_CP040429.1|WP_025877273.1|3883594_3883921_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_154881075.1|3864199_3865345_-|lytic-murein-transglycosylase-B	unknown	unknown	gnl|CDD|274066
NZ_CP040429.1|WP_134833094.1|3867551_3867962_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_025877269.1|3881765_3882527_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	unknown	unknown	gnl|CDD|234689
NZ_CP040429.1|WP_105164662.1|3862964_3864203_-|septal-ring-lytic-transglycosylase-RlpA-family-protein	unknown	unknown	gnl|CDD|223868
NZ_CP040429.1|WP_032975369.1|3861644_3862862_-|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl|CDD|224600
NZ_CP040429.1|WP_154881079.1|3879534_3881463_-|aminopeptidase	unknown	unknown	gnl|CDD|341062
NZ_CP040429.1|WP_049399252.1|3882607_3883060_+|nucleoside-deaminase	unknown	unknown	gnl|CDD|238612
NZ_CP040429.1|WP_025878706.1|3860367_3861441_+|lipid-A-deacylase-LpxR-family-protein	unknown	unknown	gnl|CDD|378338
NZ_CP040429.1|WP_154881076.1|3865617_3865866_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP040429.1|WP_032976538.1|3869382_3871461_-|penicillin-binding-protein-2	unknown	unknown	gnl|CDD|274573
NZ_CP040429.1|WP_025877247.1|3868273_3869386_-|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_CP040429.1|WP_099844396.1|3866051_3867152_-|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_CP040429.1|WP_059065157.1|3874509_3875448_+|carbohydrate-kinase-family-protein	unknown	unknown	gnl|CDD|238917
NZ_CP040429.1|WP_025877251.1|3871464_3871950_-|rod-shape-determining-protein-MreD	unknown	unknown	gnl|CDD|225444
NZ_CP040429.1|WP_032976539.1|3878676_3879408_-|lipoprotein	unknown	unknown	unknown
NZ_CP040429.1|WP_025877255.1|3873180_3874227_-|rod-shape-determining-protein	unknown	unknown	gnl|CDD|237562

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP040429.1|WP_099785438.1|3878059_3878689_-|HAD-family-hydrolase	gnl|CDD|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	2.48456e-29
NZ_CP040429.1|WP_154881078.1|3875778_3877749_-|sulfatase-like-hydrolase/transferase	gnl|CDD|224287	COG1368, MdoB, Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily [Cell envelope biogenesis, outer membrane].	1.15395e-90
NZ_CP040429.1|WP_154881075.1|3864199_3865345_-|lytic-murein-transglycosylase-B	gnl|CDD|274066	TIGR02282, Membrane-bound_lytic_murein_transglycosylase_B, lytic murein transglycosylase B. This family consists of lytic murein transglycosylases (murein hydrolases) in the family of MltB, which is a membrane-bound lipoprotein in Escherichia coli. The N-terminal lipoprotein modification motif is conserved in about half the members of this family. The term Slt35 describes a naturally occurring soluble fragment of MltB. Members of this family never contain the putative peptidoglycan binding domain described by pfam01471, which is associated with several classes of bacterial cell wall lytic enzymes. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	2.8686e-135
NZ_CP040429.1|WP_025878706.1|3860367_3861441_+|lipid-A-deacylase-LpxR-family-protein	gnl|CDD|378338	pfam09982, DUF2219, Uncharacterized protein conserved in bacteria (DUF2219). This domain, found in various hypothetical bacterial proteins, has no known function.	2.90839e-110
NZ_CP040429.1|WP_025877269.1|3881765_3882527_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	gnl|CDD|234689	PRK00216, ubiE, bifunctional demethylmenaquinone methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol methylase UbiE.	7.21976e-138
NZ_CP040429.1|WP_105164662.1|3862964_3864203_-|septal-ring-lytic-transglycosylase-RlpA-family-protein	gnl|CDD|223868	COG0797, RlpA, Lipoproteins [Cell envelope biogenesis, outer membrane].	3.3428e-52
NZ_CP040429.1|WP_032975369.1|3861644_3862862_-|D-alanyl-D-alanine-carboxypeptidase	gnl|CDD|224600	COG1686, DacC, D-alanyl-D-alanine carboxypeptidase [Cell envelope biogenesis, outer membrane].	4.78901e-149
NZ_CP040429.1|WP_154881079.1|3879534_3881463_-|aminopeptidase	gnl|CDD|341062	cd09599, M1_LTA4H, Peptidase M1 family including Leukotriene A4 hydrolase catalytic domain. This model represents the N-terminal catalytic domain of leukotriene A4 hydrolase (LTA4H; E.C. 3.3.2.6) and the close homolog cold-active aminopeptidase (Colwellia psychrerythraea-type peptidase; ColAP), both members of the aminopeptidase M1 family. LTA4H is a bifunctional enzyme, possessing an aminopeptidase as well as an epoxide hydrolase activity. The two activities occupy different, but overlapping sites. The activity and physiological relevance of the aminopeptidase is poorly understood while the epoxide hydrolase converts leukotriene A4 (LTA4) into leukotriene B4 (LTB4), a potent chemotaxin that is fundamental to the inflammatory response of mammals. It accepts a variety of substrates, including some opioid, di- and tripeptides, as well as chromogenic aminoacyl-p-nitroanilide derivatives. The aminopeptidase activity of LTA4H is possibly involved in the processing of peptides related to inflammation and host defense. Kinetic analysis shows that LTA4H hydrolyzes arginyl tripeptides with high efficiency and specificity, indicating its function as an arginyl aminopeptidase. Thermodynamic characterization using different biophysical methods shows that structurally distinct inhibitors of the LTA4H occupy different regions of the binding site; while some (RB202, ARM1 and SC57461A) bind to the hydrophobic hydrolase side, both bestatin and captopril are located at the hydrophilic peptidase side. LTB4H overexpression is associated with different pathological conditions and diseases such as cystic fibrosis, coronary heart disease, sepsis, shock, connective tissue disease, and chronic obstructive pulmonary disease. It is also overexpressed in certain human cancers, and has been identified as a functionally important target for mediating anticancer properties of resveratrol, a well-known red wine polyphenolic compound with cancer chemopreventive activity.	0
NZ_CP040429.1|WP_049399252.1|3882607_3883060_+|nucleoside-deaminase	gnl|CDD|238612	cd01285, nucleoside_deaminase, Nucleoside deaminases include adenosine, guanine and cytosine deaminases. These enzymes are Zn dependent and catalyze the deamination of nucleosides. The zinc ion in the active site plays a central role in the proposed catalytic mechanism, activating a water molecule to form a hydroxide ion that performs a nucleophilic attack on the substrate. The functional enzyme is a homodimer. Cytosine deaminase catalyzes the deamination of cytosine to uracil and ammonia and is a member of the pyrimidine salvage pathway. Cytosine deaminase is found in bacteria and fungi but is not present in mammals; for this reason, the enzyme is currently of interest for antimicrobial drug design and gene therapy applications against tumors. Some members of this family are tRNA-specific adenosine deaminases that generate inosine at the first position of their anticodon (position 34) of specific tRNAs; this modification is thought to enlarge the codon recognition capacity during protein synthesis. Other members of the family are guanine deaminases which deaminate guanine to xanthine as part of the utilization of guanine as a nitrogen source.	3.70705e-42
NZ_CP040429.1|WP_032976538.1|3869382_3871461_-|penicillin-binding-protein-2	gnl|CDD|274573	TIGR03423, pbp2_mrdA, penicillin-binding protein 2. Members of this protein family are penicillin-binding protein 2 (PBP-2), a protein whose gene (designated pbpA or mrdA) generally is found next to the gene for RodA, a protein required for rod (bacillus) shape in many bacteria. PBP-2 acts as a transpeptidase for cell elongation (hence, rod-shape). [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	0
NZ_CP040429.1|WP_025877247.1|3868273_3869386_-|rod-shape-determining-protein-RodA	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	6.82439e-146
NZ_CP040429.1|WP_099844396.1|3866051_3867152_-|rod-shape-determining-protein-RodA	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	7.49021e-145
NZ_CP040429.1|WP_059065157.1|3874509_3875448_+|carbohydrate-kinase-family-protein	gnl|CDD|238917	cd01942, ribokinase_group_A, Ribokinase-like subgroup A. Found in bacteria and archaea, this subgroup is part of the ribokinase/pfkB superfamily. Its oligomerization state is unknown at this time.	8.43181e-116
NZ_CP040429.1|WP_025877251.1|3871464_3871950_-|rod-shape-determining-protein-MreD	gnl|CDD|225444	COG2891, MreD, Cell shape-determining protein [Cell envelope biogenesis, outer membrane].	2.85269e-29
NZ_CP040429.1|WP_025877255.1|3873180_3874227_-|rod-shape-determining-protein	gnl|CDD|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0

Protein sequences

>NZ_CP040429.1|WP_025877251.1|3871464_3871950_-|rod-shape-determining-protein-MreD
MSRLRDNRWVLPASLVVALLLGLLPLPALLQPLRPYWLALVLAYWVIEAPERVGLGIAFASGVVADLLYGGVLGEQALRLVMLAFILQRFRARIRFFPMSQQMLAIGGLLFNDRIVSALVHILVGEPTLPWSYWWAPLLGMGLWPLVFVLLDAVRFGKRGR
>NZ_CP040429.1|WP_032976538.1|3869382_3871461_-|penicillin-binding-protein-2
MLPRRQVKNPHAEAEQFRRRAALGFFGVLVCLLGLGGWYFKLQVLDHDIYATRSEANRIKPRPVVPGRGMIYDRNGRLLAENVPAFRLDVTPDKVKDMDATLEGLAKIIQISPEELEAFNKSRKARRKFLPVTLKLRMSDEEMARFAVDRWRFPGVELEPYLTRRYPYGDLFAHIIGYVGRVDDKDLEILGEGNAALTHIGKSGLERYYEQELRGKVGYEQVETNVQGRAIRTIGRVAAQSGADLRLSIDADLQRAMVAAFGDQEGSAVAMDPRTGEVLAMVSLPSYDPNLFVNGISHADFKALNDNPSRPQFNRLVLGGVAPGSTLKPLIGLAGLDSGVRRPEDKVLSTGMFYLPGTSRGWGDSHRGGHGWTDLRKSIAQSVNTYYYRLALDLGIERFDHYMEYYGFGQPTGIDLTGEISGILPSPAYKRKSRKEAWYPGDTVNISIGQGDWKVTPLQLARGVSGLANGQLRTPHLVMQQRAGFDSDWVAAEPGPSKPVSPNPNNLQAVREGMMATMLPGGSAARMAAGAPYTMAGKTGTAQVVSRKGTAAVNPRSLPMHLRHRALFVGFAPAEQPVIALAIAVEGGGYGGAAAAPIARKIFDAWLLGKMPEGMQPLDSERGTTAIGITAFDNEDVNARPAGDAAAAELGEHPVLIGMPAPPPAPAPVPGSPSAAALPVGPRPTVAAEASR
>NZ_CP040429.1|WP_025877247.1|3868273_3869386_-|rod-shape-determining-protein-RodA
MSAFLRWAGEMLQRFFSSLDWLLCLALGALMVIGLATLKSAGGDGLVMAQGVRFAVGLAAMWGISRAPILRIRSATPLIYAISMIPLLAVFALGTGKYGRQWLDLKFFYLQPAELLKVSLPMMVAWYLHKMPLPPRFNTVLVAMVIIGVPTGLVMLQPDFGTGVLIAASGVFVLLLAGLPWWWVGLGVGGVAAVAPVAWFWLLRPYQKDRIMMFLDPEMDALGAGWNIIQSKIAIGSGGFDGKGWGEGSQSHLNFIPEQTTDFAFSVLSEEFGWIGVALVLTLYLVVIGRCLWIASQSRDSYSRLLAGATGLAFFVYVLVNGGMISGLLPVVGVPMPLISYGGTSAVSLLAGFGLVMAVRRHNPVHGGYG
>NZ_CP040429.1|WP_134833094.1|3867551_3867962_+|hypothetical-protein
MSASTYPYLFATLGEAAHQLPHDIARALETTLTATQAANAPGGPTLLDCLQRIRQVEAADGQPWPSKGRTQAQRMAMARIDRANAGLTFLLELLHASERVRVDGDDTQHLPDDAREGLLLACRGLSEYVDVQLQAA
>NZ_CP040429.1|WP_099844396.1|3866051_3867152_-|rod-shape-determining-protein-RodA
MPRVKWKRMLGGCREALRTIDLPLLIALLILMGAGLAVLHSVNGPVHGQAMRFAGGLAAMWLLSRVSLLRLRAWTPAIYALSMLPLMAVYVIGTGKYGQRWLNLGVFYLQPSELLKLSLPLMMAWYLHRQPLPPSPRTVLTAAVLIGVPALLILMQPNLGTATLVTASGVFALLLAGLQWRWVAAGLGAVSVAAPLAWFGLLRQYQKNRVLTFLDPAADPLGTGWNILQSRIAIGSGGMQGRGWGHGTQATLDFLPEYTTDFAFSVLAEEFGWIGVVVVFALYLFVVGRCLSIAVQARDTHARLLAGSLGLAFFVYVLVNGGMISGLLPVVGIPMPLISYGGTSAVSLLAGIGLVMAVRGHRPVHA
>NZ_CP040429.1|WP_154881076.1|3865617_3865866_-|hypothetical-protein
MLSALTHEGLRRSPTFAADARMNLRKRISVIVPTTPHSSIAADEVPLKVGANSHFDAALILINGLVAIGLHNGGPFGMARRL
>NZ_CP040429.1|WP_154881075.1|3864199_3865345_-|lytic-murein-transglycosylase-B
MIRRSLACMLTLGLVACATQPTSPPTSPQASSTPRHPAAKPHGPAEAAPEATAATAAPVDLTPVPFETARARFIADTAKRYGLKPDEIRNVLDQAQVRQPIIAAMSRPAERVKPWNEYRPMFISKARIDGGKAFLAQHRAELDRVQQRTGVPAEVIVAIIGVETSYGKNAGSHRVLDALYTLAFYYPRSGDPAKLEREVRRELFFRDELAKLFELGREEKLDITTLKGSYAGAMGMGQFMPSSYLDYAVDGNGDGRRDLFTSYDDVFSSIANYFVKKGGWVRGGQVAVPATLAAGREEFNPTEWMPTWSLADLAQRGYQPSAPVQPGATATPITLEGSTGKQYWLGFQNYYAITRYNLSKMYAMAVFHLSQAIAGQELPPA
>NZ_CP040429.1|WP_105164662.1|3862964_3864203_-|septal-ring-lytic-transglycosylase-RlpA-family-protein
MNIRWLVPGLIVLALAACSSAPKKPASAGHGGKPSGTVVQGKGGRPAHCPEGSPYAAATEDLSTRGNYTAGGLYKPGVKDTTPSYVPNVACIPEPVVTNEDRSAIGNKSPYVVLGKQYKVLDDTRNYVERGTASYYGAKFHGRLTSNREVYDMYQFTAAHKTLPLPSFARVTNLDNGESVIVRVNDRGPFHDGRVVDLSYAAAVRLGITQRGTGNVEVRAVQPGETNLMAQKPSRRERRAAEAATAAVASARPAPTARAVADSDIDRLVKRLPADAAPERGQPATTQAAVSTMPEVAVSSLPPSAPASRPAAPVVTTAMPRSPAPASSPSLSQKVVGAVMLQVASFSNRDNANRAMGQLNAAGIVGATISDIAAGGRTLWRLRVPASDHASAAELAGRISGLGFGSPQIVKD
>NZ_CP040429.1|WP_032975369.1|3861644_3862862_-|D-alanyl-D-alanine-carboxypeptidase
MNFRSAATALAATLVVGLASAQTPLPTPATPAPAAAAAPATVATPPAPAPSVSKAWVLMDYATGQVLAGENINEQLAPASITKVMTSYVIAAEVKNGKVRPDDQVMMSERAWREGGAGTDGSYSGFPVNQTARLEDMEKGMAIQSGNDAAIALAEHVAGSEEAFASLMNSYAAKIGMKNSHFVNAHGLTAPGHHSSAYDLALLGRAMVRDYPETYAYNKIKEFQVGTIKQPNRNLLLWRDGSVDGIKTGHTSEAGYCLMSSAQRGDQRLVAVVLGGASEKQRADDSLALLNWGFRFFETHRLYEPGKAVAEHKVWKGTTDKVQLGVAQPMLVSVPRGRYNDLKPSIDVPKTLEAPFTAGQQIGTVKVTLDGKLVAEAPLVAVAAVEQAGFFKRLWDSFWMWWESE
>NZ_CP040429.1|WP_025878706.1|3860367_3861441_+|lipid-A-deacylase-LpxR-family-protein
MIIPSMRYLASFGLSGLLATALPLSAYAAEQCGPDAMREHPPQVNFRVDNDLFGGRHQDQGYTNGAQLTLVSPNLVDYTDDPCLPRLARWVNSHLEALHPGRFEQQNMIFSLAQGIFTPTDFTRKDLIEDDRPYAGVLVASFGYNARSGDHLQTTQLTLGVVGPWAQGRQVQNAVHDVLGDEKFQGWDNQLHNEPVFMLTHERMRRWPGDASINADGWGWDAISHYGGSIGNLETKANVGGEVRFGWKLPDDFGSTPLRPAGENTAPTRGGKPSGWSWHMFATTDAAWVIRDITLDGNTFRNSHSVDKRHVVAYGGYGVAVMRGRWKFAVARYHSTREFNGQREAPVFGSFTISRSL
>NZ_CP040429.1|WP_025877255.1|3873180_3874227_-|rod-shape-determining-protein
MFKKLRGMFSNDLSIDLGTANTLIYVRGQGIVLNEPSVVAVRQDRAIGGTRSVAAVGAEAKQMLGRTPGHITTIRPMKDGVIADFTYTEAMLKHFIKKVHKSRFLRPSPRVLVCVPAGSTQVERRAIKESAEEAGARDVFLIEEPMAAAIGAGMPVTEARGSMVIDIGGGTTEVAVISLNGIVYSASVRIGGDRFDESITNYVRRNHGMLIGEATAERIKVELGCAYPQAEAIEMEISGRNLAEGVPKMIKISSNEVLEALHEPLSGIVSAVKLALEQTPPELCADVAERGIVLTGGGALLRDMDRLISEETGLHVQVADDPLTCVARGGGRALELVDMHGNEFFAPE
>NZ_CP040429.1|WP_059065157.1|3874509_3875448_+|carbohydrate-kinase-family-protein
MSALICGSLAFDTIMVFPDQFKNHILPDKVHILNVSFLVPRMRREFGGCAGNIAYNLHLLGGDPIPMGTVGSDFGPYREHFDALGIDLTRVRVIDELFTPQAFITTDHDNNQITAFHPGAMMRSYENHVRDVPGVSLGLVGPDGREGMIQNALEFHEDGVPFIFDPGQAMPLFNGPELREFIEQADYVVVNDYESNLLQERTGWNEKEIVSRVKAYITTRGPKGAVIHTPEKSYDIPPAHERRVVDPTGCGDAFRAGLIYGIQKGFDWLTIGRMGNLMGALKVEHPGTQNQRFTFDEFNEQFKQQFGYALNA
>NZ_CP040429.1|WP_154881078.1|3875778_3877749_-|sulfatase-like-hydrolase/transferase
MLRAAWVSLYRRLCPIAAFFLFGLVALSLSRLGLSLWHAARVSAADGWSTVLLQGLRVDVSTLCLLYGIPAVLALLLPLEGRVGRAWRHLLRWWLILASVLLVFMELATPSFMAEYGLRPNRLFLEYLIYPEEVGMTLLRGHLLAVVIEVAAVIVLFWALLRGSRRWVGNSPALAVEAGWLWRLPLALLVLLLAALGVRSSLGHRPLNPALVAFSTDPTINALPLNSLYTVGYAARQLATRSETSRVYGDLPLAEVVSELRASSGLPASAYVSDALPSLALRPPQYQGKPRNLVIVLEESLGAQFIGSLGGRPLSPNYDRLSRQGWAFERLYATGTRSVRGIEAVLTGFPPTPAESVVKLPASRQRFFTLADVLGRHGYDTGFYYGGESHFDNMREFFLANGFTRIVDRKDYRKPAFVGSWGASDEDLFARADQQFRQLKAQGTPFFGLVFTSSNHDPFEFPDGRIDLYEQPKQTRDNAAKYADYALGEFFRKAMASPYWQDTVFLVVADHDSRVFGKNMVPIGNFHIPGLILGGGIEARRDARIVSQIDLPPTLLSLLGIADATPTVGQDLTDLQRLQPGRALMQYDRNLAWMEGNDVAILQPDKPAQGFRYDPASDQLQPQPLRPELARRAHAYAMWGTLAYEKELYRLPKARP
>NZ_CP040429.1|WP_099785438.1|3878059_3878689_-|HAD-family-hydrolase
MVALTVQAPAAASSLSAIRHWVFDMDGTLTVAVHDFARIKRELAIPQEDDILTHLAGLPAAEASAKHAWLLAHERALAAASQPATGAVALVRALQGAGCRLGILTRNVRSLAQVTLQAIGLGDVFAEDDIIGRDEAEPKPSPAGLQYFLRRWQVEPSQVVMVGDYRFDLECGRAAGSRTLLVNAPDNPWPGMACWHLADCGAVLERWGG
>NZ_CP040429.1|WP_032976539.1|3878676_3879408_-|lipoprotein
MKRLILLTACTLALAACSNPEEERKAQEAAAAAVQAQKEAKAEDVAKQYDMAVAAQDWERARLHGASLLDQYKDTAAAERIAAGFDEVKAKGDAARDLRRMQALWQYNQIPVGSKGNQVSAQIFSKERVDVDGSGAKPVQLVFRDHPEWKRHAYLVLQAGDFRCPQCTVKVTVDGGKPVSMAAWRPKTDEAIAMFITDQKALWKLAAKGKSISIEFPVKAGGTRTAVFETGGVDASRMPAWWR
>NZ_CP040429.1|WP_154881079.1|3879534_3881463_-|aminopeptidase
MRNPLMLLPLAVALAAGCSQEAAAPAAAPTAQKTPAAPVNAENRSHDESSYAEPDKVVVKDIALDLKLDFDQKQIGGTATYTLEWKQKDAKQLVLDTRELSIAKVEAIAADGARSPLQFVLAPADKVFGSKLTIETPEQPAKVEVTYHTAPTASGLQWLAPSMTEGKKLPFMFSQSQAIHARSWVPLQDTPSVRFTYSAHVVSRPDVMVLMSADNDPKAARDGDYTFKMPQPIPSYLLAIAAGDLVFEPISGRSGVWAEPTMVNKAAKEFEDTEKMIGAAEKLYGEYRWGRYDMLVLPPSFPFGGMENPRLTFATPTVIVGDKSLVSLVAHELAHSWSGNLVTNASWKDIWLNEGFTTYVQGRITEALYGKEMAEMEKQIDQTDLLAEVKDMSPADQALALPPLNERDPDEALSQVAYVKGSWFLEFLEQRFGRETFDPFLRGWFDDHAFQSANTDQFVEYLKKNLLPKNPSAVTEAELKAWLDEPGIPAFAAKAQSRNFSSVDTARIAFASAGTVPSSQVIAEWSTQEWVRFIDGLGATQPLDKLATLDKAFHFTGTPNGEIAMRWYPLTIRSGYEQANEAAAAFIERVGRRKLILPIYAELVKTPKGLELAKQAFEKAKPGYHPITTASVQDMLAKAEAK
>NZ_CP040429.1|WP_025877269.1|3881765_3882527_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE
MSESPYKSGTTHFGFRDVDAKDKQKLVGQVFTSVARNYDLMNDLMSMGVHRAWKRYYVATAQVKPGDRVLDLAGGTGDIAALLKERVGAEGSVVLGDINAGMLSVGRDRLTNRGLVLGLDYVQCNAEALPFPDNSFDLVTIAFGLRNVTDKDAGLREMFRVLKVGGQARVLEFSEVTADWFKPIYDFHSFKILPKLGKLFANDSDSYQYLAESIRKHPPQEELKAMMGQAGFERCHYKNLTGGIVSIHSGYKL
>NZ_CP040429.1|WP_049399252.1|3882607_3883060_+|nucleoside-deaminase
MITTPDYQALLQTAIAEARQGLAEGGVPIGAALYHNDGRLLGCGHNRRVQEGDPSVHGETDAFRKAGRQRRYQDTIMVTTLAPCWYCSGLVRQFNIGTVVVGESRTFQGGIDWLRENGVNVIDLDNQECVDLLGGFIAQHPEIWNEDIGE
>NZ_CP040429.1|WP_025877271.1|3883259_3883520_+|hypothetical-protein
MQAHAVRPRSDPALAAIWSRLQQQYALHQRSAPFWSAYQDMQQDLLHDHPRDLVRLCNAMAAMAERLGAVEHAQLLRHRHAGCTSR
>NZ_CP040429.1|WP_025877273.1|3883594_3883921_+|hypothetical-protein
MHAEVPAIPPVINVDAELDYWRRQHADGALAHTSFGTYVPWIKFACDSLITQPRASNAQRDELFQTQYALQIMPRLSEAQAREFVERCWQHVYLASPVRSQEAPRLRA

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_AP017656	Sphingobium cloacae strain JCM 10874 plasmid pSCLO_2, complete sequence	919-945	4	0.852
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	505799-505825	4	0.852
NZ_CP040429_4	4.1|393526|27|NZ_CP040429|CRISPRCasFinder	393526-393552	27	NZ_CP054032	Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence	1093999-1094025	4	0.852
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	CP000663	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence	123001-123027	4	0.852
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	69169-69195	4	0.852
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	277143-277169	5	0.815
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	2035104-2035130	5	0.815
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	967152-967178	5	0.815
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_CP021802	Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence	580397-580423	5	0.815
NZ_CP040429_4	4.1|393526|27|NZ_CP040429|CRISPRCasFinder	393526-393552	27	NZ_CP045288	Curtobacterium flaccumfaciens pv. flaccumfaciens strain P990 plasmid pCff1, complete sequence	112643-112669	5	0.815
NZ_CP040429_4	4.1|393526|27|NZ_CP040429|CRISPRCasFinder	393526-393552	27	NZ_AP014708	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_4p, complete sequence	12969-12995	5	0.815
NZ_CP040429_4	4.1|393526|27|NZ_CP040429|CRISPRCasFinder	393526-393552	27	CP041260	Curtobacterium flaccumfaciens pv. flaccumfaciens strain Cff1037 plasmid pCFF113, complete sequence	107086-107112	5	0.815
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	HQ632858	Tetraselmis viridis virus SI1 genomic sequence	9225-9251	5	0.815
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	NC_020840	Tetraselmis viridis virus S20 genomic sequence	21207-21233	5	0.815
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	NZ_CP032695	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence	376369-376395	5	0.815
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	978197-978223	6	0.778
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	111284-111310	6	0.778
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	123999-124025	6	0.778
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_LR594669	Variovorax sp. SRS16 plasmid 4	39411-39437	6	0.778
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	768370-768396	6	0.778
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	NC_022001	Streptomyces collinus Tu 365 plasmid pSCO1, complete sequence	39149-39175	6	0.778
NZ_CP040429_4	4.2|393580|27|NZ_CP040429|CRISPRCasFinder	393580-393606	27	NC_010182	Bacillus mycoides KBAB4 plasmid pBWB403, complete sequence	31999-32025	6	0.778
NZ_CP040429_3	3.1|393358|27|NZ_CP040429|CRISPRCasFinder	393358-393384	27	MN585195	Pseudomonas phage AUS531phi, complete genome	8552-8578	7	0.741

1. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_AP017656 (Sphingobium cloacae strain JCM 10874 plasmid pSCLO_2, complete sequence) position: , mismatch: 4, identity: 0.852

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
gtccacgcggctgccgaccagccggat	Protospacer
*. ****************** * ***

2. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 4, identity: 0.852

gcgca-cgcggctgccgaccaggccgat	CRISPR spacer
-cgcgtcgctgctgccgaccaggccgaa	Protospacer
 ***. *** ***************** 

3. spacer 4.1|393526|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP054032 (Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence) position: , mismatch: 4, identity: 0.852

cgtgcgcgcacgatcggcgaccttgac	CRISPR spacer
cgtgcgcgcacgaacggcgaacttctc	Protospacer
************* ****** ***  *

4. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to CP000663 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence) position: , mismatch: 4, identity: 0.852

ggtttccacgccttcgccgacacggat	CRISPR spacer
gggttccacgcctttgccgacacggtc	Protospacer
** ***********.********** .

5. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 4, identity: 0.852

ggtttccacgccttcgccgacacggat	CRISPR spacer
gggttccacgcctttgccgacacggtc	Protospacer
** ***********.********** .

6. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 5, identity: 0.815

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
gatggcgcggccgccgaccaggccgat	Protospacer
*   .******.***************

7. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 5, identity: 0.815

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
ctgcacgcggccgccgaacaggccgag	Protospacer
 .*********.***** ******** 

8. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
ctgcacgcggccgccgaacaggccgag	Protospacer
 .*********.***** ******** 

9. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP021802 (Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence) position: , mismatch: 5, identity: 0.815

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
gcgcacgaggctgccgaccagcaggtt	Protospacer
******* *************   * *

10. spacer 4.1|393526|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP045288 (Curtobacterium flaccumfaciens pv. flaccumfaciens strain P990 plasmid pCff1, complete sequence) position: , mismatch: 5, identity: 0.815

cgtgcgcgcacgatcggcgaccttgac	CRISPR spacer
cgtgagcgcacgatcgccgacctcctc	Protospacer
**** *********** ******.  *

11. spacer 4.1|393526|27|NZ_CP040429|CRISPRCasFinder matches to NZ_AP014708 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_4p, complete sequence) position: , mismatch: 5, identity: 0.815

cgtgcgcgcacgatcggcgaccttgac	CRISPR spacer
ctggcgcgctcgatcggcgaccttcag	Protospacer
*  ****** ************** * 

12. spacer 4.1|393526|27|NZ_CP040429|CRISPRCasFinder matches to CP041260 (Curtobacterium flaccumfaciens pv. flaccumfaciens strain Cff1037 plasmid pCFF113, complete sequence) position: , mismatch: 5, identity: 0.815

cgtgcgcgcacgatcggcgaccttgac	CRISPR spacer
cgtgagcgcacgatcgccgacctcctc	Protospacer
**** *********** ******.  *

13. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to HQ632858 (Tetraselmis viridis virus SI1 genomic sequence) position: , mismatch: 5, identity: 0.815

ggtttccacgccttcgccgacacggat	CRISPR spacer
ggtttccacgccatcgccaacacccag	Protospacer
************ *****.****  * 

14. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to NC_020840 (Tetraselmis viridis virus S20 genomic sequence) position: , mismatch: 5, identity: 0.815

ggtttccacgccttcgccgacacggat	CRISPR spacer
ggtttccacgccatcgccaacacccag	Protospacer
************ *****.****  * 

15. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP032695 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence) position: , mismatch: 5, identity: 0.815

ggtttccacgccttcgccgacacggat	CRISPR spacer
tttttccgcgccttcgccgacacctat	Protospacer
  *****.***************  **

16. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 6, identity: 0.778

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
gcgcaggcggctgccgacccggcgctc	Protospacer
***** ************* ***   .

17. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.778

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
cggcacgccgctgccgaccacgccgcg	Protospacer
  ****** *********** ****  

18. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.778

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
cggcacgccgctgccgaccacgccgcg	Protospacer
  ****** *********** ****  

19. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_LR594669 (Variovorax sp. SRS16 plasmid 4) position: , mismatch: 6, identity: 0.778

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
cagcacgaggctgccgaccagggcgcg	Protospacer
  ***** ************** **  

20. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.778

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
gcgcacgcggccgacgaccaggctccc	Protospacer
***********.* *********.  .

21. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to NC_022001 (Streptomyces collinus Tu 365 plasmid pSCO1, complete sequence) position: , mismatch: 6, identity: 0.778

ggtttccacgccttcgccgacacggat	CRISPR spacer
ggtttccccgccttcgccgacgaagca	Protospacer
******* *************. .*  

22. spacer 4.2|393580|27|NZ_CP040429|CRISPRCasFinder matches to NC_010182 (Bacillus mycoides KBAB4 plasmid pBWB403, complete sequence) position: , mismatch: 6, identity: 0.778

ggtttccacgccttcgccgacacggat	CRISPR spacer
aagttccacaccttcgccgacaccgac	Protospacer
.. ******.************* **.

23. spacer 3.1|393358|27|NZ_CP040429|CRISPRCasFinder matches to MN585195 (Pseudomonas phage AUS531phi, complete genome) position: , mismatch: 7, identity: 0.741

gcgcacgcggctgccgaccaggccgat	CRISPR spacer
ctcgtcgcggttgccgaccaggccgaa	Protospacer
 .   *****.*************** 

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	279577 : 297214	19	Siphoviridae_environmental_samples(33.33%)	tail,head	NA
DBSCAN-SWA_2	622625 : 631603	7	Enterobacteria_phage(42.86%)	NA	NA
DBSCAN-SWA_3	1645080 : 1705758	65	uncultured_Caudovirales_phage(15.38%)	protease,tail,portal,terminase,capsid,head,integrase,tRNA	attL 1674636:1674651|attR 1708695:1708710

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP040429|279577:297214|DBSCAN-SWA
GATGCCCCTGCTGACACTTGAGCAGTGCCGCATGCACTGCCGTATCGACGGCGACTACGACGACGCCATTCTGGACGACCTGCTGGCCGCGGCGACCGACGCGGCGTCGGCCTACCTGCGGCGGGCGCTGTTTGCCGACCAGGCGGCACTGGATCTGGCGCTGGACCAGTTGCCGCAGGACATGGCGGCGGCGGTGACCGGGCATGAAGCCGCGGTCGCCGCCGCCAATGCCGAGACCAACGCGGCCAAGGCCAAGGCCATGCGTGACGTCGCTGATCGTCGCCTGGCCGCGGCCACCGAACGCAGCGCGCAGCTGCTGCAGGGCCTGCCGGCCAACGACAGCATCCGCGCTGCGGTGCGCCTGCTATTGGGCCATCTGTATGCGCATCGGGAAGCGGTGGTGGTTTCCACGCACGCCTTGGATATACCGGTCGGTGCTGCCGCCATCGCGATGGAGCTGCCGTTTGGCATCGCCGCACTGCTCGATCCCTACCGACTGGCGGCGACCCCATGAACGCCGGTCACTTCAACCGTCGCATCCGCATCGAGCGCCAGGATGGGCGCGTCGATGCCTGGGGCCAACCTCTGGATGCGTGGGTGAGCGTTGCCGATCTGTGGGCGGCAATTCCTCTTGAACGTGCCGACGCGGTGCAGCGGGTGAAGCTGGACAGCGGGCTGTCCGCAGCGATTCGCCGCCAGCGCTTCCAGGTGCGCCTGGCACCGGCGCAGCGAGCCGGCATTGGCATCGGAATGCGCATCGTGCACGACGGCCACACGTTCGATATTACCGGTGTGGTGCCCGACCTTGGCACGCGACACACCGCCGTGCTGTTCACCGAACAGCTGGCTGCAACCGCCTGAGCGAGGACACTGCGATGAGTTACGAACCGAAGTTGCAGCAACTGCTTGGCGGATTGCTGCAGGGGCGCCTGTACCCGGATGTTCCACCGGACCGAGTCACCTATCCCTGCGCGGTCTACCAGCAGGTGGGTGGGCAGGCGCTGTGGTTCAACGAAGGGTCCATCCCCGACCAGAAGCACGCTCGCGTGCAGCTGACCGTCTGGGCAGACACCCGTGCCCAAGCCAACACCCTGATCCGTGACATCGAAGATCAGGTCTGCGCGGGTCTGCCGAAGTCTGAATCCTTTGGCGCCGCCATTGCCGTGCATGAACCGGCACTCAGGAAGTACGGCGCACGGCTCGATTTCGGGCTGTGGTACGCCAACCCGTAGTTCCACTGCTCCACGTACCACCTGAAGCCCGGCATACGCCGGGCTTCGTCTTTTTCAATCCACATGAGGAAATGCAACATGGCACTCAAGCTTCCCAAGGGCACCCAGTTCGGCTTCGCACCGGTCGTCTCCACCGCCATCGCCACCAGCGCGATCTCCAAGGCTGCGCCGGCACTGGCCAGCGTCGCCGCCAACAGCGTCGACACCGGCGATGTGGTGGTCATCGAGCTGCCGGGTTGGCCGGCCCTGAACAACCGCGCTACCCGCGCCGGTGCCGAAGCCACCGGCAGCGTTGAACTGCTGGGCATCGATACCACCGACAACGTGCTGTTCCCCGCCACCAGCGGTGCCGGCGTGCTGCGCAAGGCCGGTGCCTTCGTCGACCTGGACCAGCAGGGCGACCCGACCACCGCAGGTGGCGAGCAGCAGTACTGGAGCGGCACCCTGCTGGAGGACCCGACCGGTCGCCAGGTGCAGATGCCGACCTTCAAGAACGCCAAGACCATCACCCTGCCGCTGTTCTACGATCCGAAGAAGCCGTGGTACTCGGCCCTGAAGAACGTCGACGCCAAGGGCGAACCGGTGATCCTGCGCGCCAAGCTGGTCGGTGGCGACGTGCTGTACTGGTACGGTTACCTGAGCTACAACGGCGACCCGACGATGGCCGCCAACACCCCGATGGGCACCACCGCGACGTTCACCGCGCTGGCCGACTCCATCCTGGTCGAGGGCGCCTGATGTTCCAGGTAAAGGCGCCAGAGAGCTTCAAGAGCACCCTGACCATCATCGGTCATGGTCGCGAGCAGAAGCTCAACCTGACCTACCGGCACCTGCCGGTGGCCGACTATGCGCAGCTGCTGGAGCGCCTGGGCGATGACACGCTGAGCGTGGCCCAGGCGATCCTGGACATCGTGGTGGATTGGGATGCCGACGTGCCGCTGGACACTGCCGGCGTCGAGCTGGCCCTGCAGCAGCAGGCCGGCCTGGATGGCGCCATCATCGGTGGTTACACCCAGGCCCTGCAGGTCGCACGCAAGGGAAACTGATCGAGGCGGTGGGGGCCCTGTACTGGCGGGCCCCCACCGAGTCCGAGCTGATGCAGCTTGGATTGAAGGCCAAGCATTTTCCGCCGCCACGGGTTGAGCTGTGGCCGGAGTGCGTGCTTCCCATCGAACTCTTTTCGCGGGTTGCCACCCAGTGGCGCGTCGGCGCAGGTGGCCCGATCGGGCTGGATTACAACGTGGTCTACCGGGAGCTGGAGCGCGAAGCGCTCGATGGCGACCAGTACGACGAGGTGATGGCGGCCATCCGCGTCATCGAACGCGCTGCCCTGGAGCAGATGCAGCAGGAATGAGCCGGCCATCGCGGCAACGCCGATGCCCGGTCCCGACTCCGCCGATGCGGAGCCGACTCTCCCGAGGAACACTCAATGAGCACTACATCGCTTGGCAGCACACGGGCCACCGTGGACGCCAGCAATGCACTGGAAACGGCCATGCAGGCAGCAAGGCGCAGCATGACCGAGATGACCGGCACCACACAGGAGTTCCAGCGGCAGCTGGAAAAGATCAATACCGTGCAGCAGGCATTCAACGCCGTGCTGACAACCAGCGCCTCGCTGGTCACCGCCCTGTCCACGCAACTGACTGCCCTGAACACGCAAATGCAGGCGGTGGCGAAGTCTGCTACGGCCGCAGCGGGCGGTGACGCGGGCAAGGCCGCGAAGGCGGAGGAGAAGGCGGACAAGGACGACATGGGCCTGGCGGGCATCCGTAAGGGTCTGGGCGGCGCGCTCGGCGACTATATCGGCAAGACCGAGAACACCGCCACGGCCGCCAAGAAGGCCTTCGGCAAGGCATTCACTGGCGCCGACGAGGCGCTGCGGAGCTTTGTGACCACCGGCAAGTCCAAGTACAAGGAGCTGGCCCAGTCCATCCTGTCCGACCTGAAGATGATTGCCGCACAGCAGGCTCTGGTCTGGGGAGCGAGGAAGATCGCCGGCATGATGGGTGTCGACCTGGCGCCCAAGGACGCTGCGACGGACGCGGCGGCAGCTGCAGCAGGCGTGGCAGCTCCCAAGGATGCCAAGGCCGGCGATGCCAAGGCAGGTGATACCAAGGGCGGCAAGGATGACAAGGACGCCAAGGGGTTTTCGGGGTTCCGCAAGGGTTTCGGCAGCGCGCTCGGCGAGTACATGGAAAAAACCGAGAACTCCGCCAAGACCACCCAGGATGCATTTTCCAAGGCATTCACCGGAGCCGAGGCCGCATTGCAGAGCTTCGTGAAGACGGGCAAGTCCAATTACAAGGAACTGGCCAAGTCGATCATCGCCGACCTCAAGATGATCGCCATCCAGCAGGCAATCGTCTGGGGCGTCAAAAAGATCACGGGCATGCTCGGTTATGGCACGGGGGTGGAGGCCAACGCCAAGGGTGGTGTCTACCAATCGCCGAGTCTGTCGGCCTACTCCGGCGGTATCTACAACACCCCACAGCTGTTCGCATTCGCCAAGGGCGCCGGCGTGTTCGGTGAAGCGGGGCCTGAAGCGATCATGCCGCTGCAGCGCGGGCCCGATGGCCGCCTGGGAGTGGCGGCACACGGTGCCGGTGGCGGGGTGGGAGTCAATATCCGCATCGACAACAACGGTGGCAAGGAAGTCACCAGCAACGAAAGCATGCTGCAGCAGTTCGGCAACGAGATCGGCCAGTTCGTGGAGCGAAAATACCGTGATCTGCAGATGCGTGACATGAAGGCTGGCGGCGTCCTCAGCAGGAGTGCAGCACGATGACCGACACCTTTACCTGGGCAGCAACCAGCCAGAGCACTGGCACCACCACTGCCACCGTCAAGCGCGCGCGCTTCGGCGATGGATACGCACAAGCCGCGCCGGATGGGCTCAATGCCCGCCTGCGCAGCTACCAGCTGCAGTTCGTCGGTAATCGCAGCACGATCAACGAGATCGTTGCGTTCCTGGATGGCCATGTGGGCCAGAGCTTCTTCTGGCGGGGCCCGCTGGGCACCGGTCTGTATGGCTGCGACACCTATACCGACAGCCATCTGGGTGGATCGGTGTTCAGCATCACTGCGACGTTCGAACAGACGTACCAGCCGTAGGAGCGGACATGGATCTTCAGCAGATCGACCTGGACACCCTCCAGCCCAACGGCAAGCGGGGCGAAACGCAGCGCCCCGCTTTCACCAAGATCAACCAGAATTTCAAGGAAGTGGCCTTGGCGGTGGATGCAGTTCCCGAGGCGGTCGCACGTGCGGTCTCGGGAAGAAATCGCCTGATCAATGGCAATTTCGACTGCTGGCAGCGGGGTACCAGCTTCAACACATCGGGAAGGTACACGGCCGATCGCTGGTTCCTTCAGATGCAGGGCATCGCCGATCCGGTATTCAGGCGGAACCCCACGGCAATGGGAGACAACAATTTTCCCCGGAGCAAGTACACGCTGTCCGTCAGCTCGAGTGGCAACACCGACGCAGAGAAGCATTTCTTCGTGTTCGAGCAACGTGTGGAGGACGTGCGAACCTTCGCCGATACCCCAAGCACGGTGTCCTTCCTGGTATTCAATGCAGGTGCGGGGGGGCGCAGGATCGCACTGGAGTTCGCGCAGACCTTCGGCGCAACGGGCAGCGCTCCGGTACTGGCCGTTGCACCTGAGATTTTCGAGCTCGCTCCTGGCCTGAACAGAATCCGCAAGACAGTGACGCTGCCCTCCATCTCGGGAAAAACACTATCTGATGAAGGTGCCGTCGTGATGTGCGTGTGGGTATCTGCGGGCACGCAGTTTGCCAAGCGCACCGCCGGCCTTGGTGCGCAGCATGGCCAGGTCTACTTCGGAGAATTCCAGTGGGAGCGCGGCGCTACGGCCACGGCATTCGAATGGCGTTCGCTGGACGAAGAAGTGCAGCGTTGTCGGCGCTACTACCAGGCCGATGCCACGGGTTCCTACTTTGACGGCGGAGTTCGCTTCAACGCTGGTGTCGGCCTCATCCGTGGTGACAACAAGGTGTACCTGATCTATCCATTCAGCCAGCGGATGCGGACCATCCCCACGGTCGGATTCTCAAACCTGCCGCAGTGGCGACTCCTTACGGGATCAGGGGCGACGAGCCTGACGGCGCTCAACGCGGTCGAAGTGTCTTCGACGAGGATGACCATCATCGGGTCCTTGAACGAAGCCGCTGCCGGTCAGGCCGGGATCCTGCAGAGCGCAGACTCCGCTGACGCGGGTACCGGAATCAGCCTGGACGCGGAAATCTGAGATCCGCGAGCACCGCTGCGGAATGCGCTGCTTTGGTGCAATCCCCGAAAAGACAAGGAAACAGCAGAAATGTCACGACGAATCATCGACCTCGATTCCATTCAACCGAATGGAAAGCGGGGTGAAACACAGCGCCCGGCCTTCACCAAGATCAACGAGAACTTCGCAGAGGTCTACGATGCCCTGGCCGCGGTGGAAAAGCTTCCAGAGACGGTGGACCACGCGATCAGTGGGCGGTTGCCCGGGCGCAATCTCTTCATCAATGGCGGCCTGCAGTTCTGGCAGCGTCGCACTTCTGGACGTGTCGGCAGCGGCTCGGGAACACTGGGTGCAGAAACGTTCTTTGCTGATCGCTTCTCCAACTCTGCGTTGAGCTGCAGTCATGACATCCAGCGCGTACCGTACGAGGGACAGTTGGGCTATCCCGAAGACACCCGCGCCATCCTCGTGTGCACGGTATCCGGTGCAGTCGCCAACAGCGGCGCCTGGATGGGCCAGAGAATCGAAGGTGTGCGAAGCGCCAGCGGCGCCGTCACGATCTCGGTCTGGGCGAACAGCGACGTAGCCGGGCGCAAGGTGGGTGTGCGTGTCATCCAGGATTTTGGAACCGGTGGGACGCCTTCGCCTCAGGTTTCCACCGAGGCGGGCGTCCTCACGTTGAGCACTGGAGCGTCGCGTCAGTCACTCACCGTGACGTTGCCGAGTACGAAAGGGAAGAAGCTGGGGGCCAACGGCAACGACCACATTTACGTGGTCTTCGATCTATGCGCCGGAGGCTACGGCGGGGCGTTGGCAGGCCAGAATGGATCCTTCGGCTTTAGCCAGTTCCAGGTCGAACCTGGGCGCAATGCAACGAACTTCGACTGGCGGCCGCCCGGCGTGGAGCTGGCCCTGTGCCAGCGTTACTACGAGAAGAGCTACAACCTGGATGTCCCGCCCAATACGCCGCACAACGAAGGACGCGAGGCATTCTCGTTGAACAACCCGGGGGTTGCCCACTACCAGAGCGTGCGCTTCCTGGTGGCAAAACGTGCGCACCCCTACGTGATGATCATTTCGGCTGATACCACCCAGCAGGATGGACACATCGCCGAGGACAACATCTCCCGTGTTCCCTGCGTAGTGAACTACGCCTCGCCATCCAGCTATGAAGTGAGTTGGTCGAACAACCCGGGCCGATGGGGCGGCTGGTGGCATTGGTGGGCCGACGCTGAGTTCTGATCCGTAGCGGTCTCTCACCAGAACAATAGGATCCCGACATGACAAGAAAGATTATCGACCTCGACACCATTCAGGCGAATGGTAAACGGGGTGAAACACAGCGCCCGGCTTTTACCAAGATCAACGAGAACTTCGCCGAGGTGTATGGCGCTTTGGGGAGCGTTGCAACCATCGTGGAGGACGTCGAACAACTGAAGACGGAGATCCAGGCAGAAGCAGACCAGGCAAAGGTGGAGGTGCAATCGGCCATCGCAGCACTTCCGTCCGCCGTCGACAACGCCATCCATGGGCGCATTCCCGCCAAGAACCGACTCATCAATGGCAACTTCGACTTCTGGACAAGAGGAACGCCGGTGATGCAGACCGGCTATGGCCCGGATCGATGGTTCGTTCAGATTGGATCGATGGTCGATGCTGGCCTTTTTGCAAACAACAACGTGCCGGGGGACGGTGTATTCGGCGATGCGCGTCTCTCGATGGGTGCCAATTCGACCGGCAACAGCGATGCGTTCGGGCACTACTTCGTGTTCGAACAGCGGGTTGAGAATGTCCGTACGTTCGCTGGTGTACTCAGCACTGTCTCCTTCACCGTCTACAACTCCGGAGCGGCCGGGAGGAAAATCGCAGTGGAGTTTCTGCAGAATTTCGGCACCGGCGGCTCTGAAACAGCCTTGGGACTGGACGCAGAGGTCTTCAGCCTGGATGTGGGTATCAACCGCATCAGCAAGACGACCACGCTACCGTCGGTCTCCGGTAAGACAGTGGCGAGCACGAATCACTATGCGGCAGTTGCCGTGTGGCTGTCATCCGGCAGCGGATTCGACGTCCGGAACGCTGCACTCGGGGCGCAGTCAGGGCAGTTGTTCTTCGGCCAGTTCCAATGGGAGGAGGGAGGTACCGCAACTGGCTATGACACCAGGCTTCTGTCCCATGAAGCAGCCCTGTGTGGCTGGTACGCGCAGCGCATCGACATCAATGCGGGAGATGCATTCTCAGTATGTACGGCCCTGGGGCAGTTTGACTGCGTAGGCCAGTTGGCATTCCAACCGATGCGCAGCAAACCCTCGGCGCGGACCCTTGGCAACGGTGTGAACATGACCGGATTTGGCATCAACGGGGGCAACGCTCCCGGCTCGTCCTTCAACGTCATCCCGGTTTCAGTATCGAGCGCAGCGATTACGGCCGGGGTTGCAACGGGTGGCATGTCACCAAATGCCTCGGGCTACGTCGCACCAAAGACTGGTGGGATCAGCATCATCTTCGAGGCGGAGATCTGACACCAAACACCGTTCATATTGGCCAAAGCGCCAGGGCCAGCCGCAGTGCCGGTCATTCAGAATCAGGAACACAGCAATGGCAATGAAAATCATCGACCTCGATACCATTCAAGCGAATGGTAAGCGAGGGGAAACGCAGCGCCCGGCGTTTACCAAGGTCAACGACAACTTCGCCGACGTCTACGCAGGCCTGGACGGCGTACAGACCGCCGTGGACGGCCTGGAAAGCCGAATGGCAGGCCGCAACCGCCTTATCAACGGTGACTTCCGGGTCTGGCAAAGGGGTACGGCGTTTTCCGCATCTACCGGTGCCCGTCCTACCGCCGATCGCTGGCTGGTGAACGCGCACGCGACCACTCTCTCTGCATCGCGCGACGACATTGCGGCAGGCGGTGGTGCGGCGGGAAGGCTGATTGCAGGTTCCCGTCACCTGCTGAAGCTCGTCGTCGAAAGTGTTGCCGGCGCCGACAGCATGGCACTGGTGCAGCAGCGCATCGAAGACGTGCGTACGTTCGCGGGAAAGCGGGTCACCGTCAGCTTCAAGGCGAGGGCCACGGTCGACAACTTCAAGGTGGGCCTGGAATTCCAGCAGTCGTTCGGCGCCGGCGGCTCAACGGCAAGGGACAGCATCGGCGGAGGCGTCACGCTCGATACGATGTGGCGCTGGCACCAGTTGACCGTGGATGTGCCTGGCATCGCAGGGCAGACCCTGGGCGCGGACAGCTATCTACAGCTCAGCCTGTGGCTGGACGCGGGCGCGAACTTCGCCGGTCGCGCGTTCGGGGCGGGACAGAAGAGTGGCGTGGTCTATCTGGCTGAAATGCAGGTCGAGGAGGGTGAGATCGCGACCGATTTCGATCGCCGGCCCGAAGCGCTTGAACTGTTGCTGTGCCAGCGCTACTACGAAACAGTTGATGTGAACCGGATCCTGGGAATCACCTACACCGCCAACGGCGATTCGCGCGCCTGCATCCCGTTCAAGGTACGCAAGCGCGTGGCGCCCAGGATCACCTCGCCCTCCACCGCGCTCAACCTGGTGGGCTTCGGCTCCGAAGGCAGTCTCATCAACTTCAACGGCGGCGATCCGGGCTGGCAGTCCACCGTGGACGCGGCCGTGTTGTCCTCGATGTCCAACAACATGCAGCAGTGCGGACCGGTCGTGGTGTGGTCGACCACCTCCCAGGTTCTGGTGCACGCAGACGCGGAGCTCTGAGCCATGAGCGCAATCACGACCGAAACCGGCCGCGTCAGCGGCTTCACCACCAATGCGTCACTGCGCCCCGGACACCGTGTGATCGTGCCCTGCGGTCAGCCGTCCCATCCCGTACCGCCTTATCCCGCCACCGCTCAGGAGCGCACCTCATGATCACCGCCGATGCCCAGCAACTCGAGCCGGGTGGCCGCATTACCGTCTTCGAACTGGACGCCAGCAGTTTCGGTGCCGACCAGCTGTTCTTCCACGCGCACCTGCAGAGCGGTGTGATCATCTGGCAGGGGCAGGAGTACGGCCCCTGGCCGATCGAAGCCAGCGGCTTTGAACGAACCAGCGACCAGCCGCCGAACCCGAAACTCCGGGTCAGCAACATCGATGGCCGCATCACCGCGATGTGCCTGCTGTTCGATGATCTGGTCGGCGCCCGTGTCATCCGTCGGCAGACGCTCGCCAAGTACCTGGATGCAGCCAACTTCGAAGAGGGCAATTCCAGCGCCGATCCGGCAGAACACTTCCCCGACGAGGTCTGGTTCATCGAGCGCAAGGTCGGTGAGGACAAGCAGACGGTGGAGTTCGAACTGACTACGGCCATCGACCTCAATGGTGAGCAGTTGCCTGGTAGGCAGATCATCGCCGGCATGTGTGGCTGGCTGGTGCGGGGTGGCTACCGCGGCCCTTACTGCGGCTACAACGGGCCGGCGGTTGCCGATGGCGACGACGTGGCCACCGATGACCCCGCCCGCGACCAGTGCGGGGGCCGTGTGCGCAGCTGCAAGATGCGTTTCGGCCAGGACAAGCCTTTGCCCTATGGCGGCTTCCCGGCGGCCGGCCTGCTCCGCTCCTGATCCAGCGCTTCCGATTCTCCACTTCCAGGCCCGCTCGCGCGGGCTATTTTTTTGGGTGAAACATGCAACCAACAACCCTGCAGGCCATCCAGGCACACGCCGTGGCCGAGTACCCGCGCGAGTGCTGCGGGCTGATCGTGGCCATCGAAGGCCACGAGCACTATTTGCCGTGCCGCAACCTCGCGGGCACACCCAGTGAACACTTCCGCCTGCCGGCCGAGGACTATGCCGTGGCCGAGGACAAGGGCGAGGTGCTGGCCCTGGTGCACAGCCATCCGGACGCAGCTGCCACACCGTCCGACGCGGATCGGGTGATGTGCGAGCACAGTGGCCTGACCTGGCACATTGTCAGCGTCGGTCAGGTGGATGGCGAGGCACCCGAATGCGGTGACCTGCAGACCATCCAGCCGAACGGCTATGTTGCGCCGCTGGTCGGCCGCCAGTTCACCCACGGCGTGCTGGACTGCTACAGCCTGGTGCGCGACTTCCATGCGCGCGAACTAGGCATTTCCTTGTCCGACTACACCCGCGACGACGACTGGTGGGACAAGGGCCAGGACCTGTACAGCCTTGAACGACTGCATGCGGAAGGCTTCGACCTGATCGAGGGCGAACCGCAGCGGGGCGACATGATCCTGATGCAGATCCGCTCGCCGGTGACCAACCACGCCGGCGTCTACCTGGGCGACGGGCAGATGCTGCATCACCTGCATGGCCGCCTGTCCGAAACCGTGCCCTACGGCGGCATGTGGGCCGAGCGCACCCGTTGCATCGTCCGCCATCGCGAGGTGCGCCATGACTGACCGTCTTCGTACCATCCGCCTGTACGGCAAGCTGGGCGCGCGCTTCGGGCGCAAGTTCCGGCTGGCGGTGAACAGCCCGGCCGAGGCCGTGCATGCCCTATGCGTGATGCTGCCTGGCTTCCAGCAGTACCTGATGGGCGCCAAGTCCAAGGGCATGGAGTTTGCCGTGTTCAACGGCCGGCAGAACCTGTCGCGGGATCAGCTGCACGACCCGCCAGGGCAGGATGACATCCGCATCGCGCCGGTGATGGTGGGCAGCAAACGGGGAGGCGTACTGCAAACCATCATTGGCATCGTGCTGATCGTTGTGGGGAGCTACACATCTTGGGCTGGCGGAGCTGCACTGGTATCAACCGGCGTCAGCATGGTGGTTGGCGGGATCACCCAGATGCTCTCCCCCCAGCCAAAAGGCCTGGGGGCCAAAGACACACCCGAAAACGCCCCCAGCTACAGCATGAACGGCACCGTCAACACGCAGGCGCAAGGCAATCCTGTTCCGGTGGCCTACGGCGGCCATGACAAGAAAGGCATGTTCATCGGCTCGGCCGTGATCAGCGGCGGCATCCTGGCGGAGGACCAGTTTTGAACCAGATCATTCATTCCGCACAGCGTGAGCGCAGTGCACCCATACCCACACTGGCCGGCGCAAAAAAGGGCGCCAGCAATGCACGCACGCCGGTGGAAACGCCGGACAGCCTGCACTCGATGGCAGTGGCCCGCATCATCGACCTGGCCAGTGAAGGCGAGATCCGTGGTCTGGTAGCGGGCAAGCAGTCCATCTACCTGGACCAGGTGCCGATCGAGAATCCGGACGGCACGCTGAACTTCTCGGGCGTGGACGTGCAGACGCGTTCGGGCACCCAGGACCAGGAGCACATCAGCGGCTTCCCCTCGATCGAGAACGAAGTCGGCGTCAACGTCGAACTGCGCAGCGATGCGCCGGTGGTTCGCACCGTGTCCGGTGCCGATCTGTCGGCGGTGCGCATCCGCTTTGCGGTGCCCGCGCTGCAGAAGACCAACACCGAAAACGGTGATACCGAGGGCTATCGCATCATGTATGCGGTGGACCTGTCCACCGACGGCGGCCCGTTCAGCACCGTGTTGAACGACGCTTTCAGTGGCAAGACCACCAGCCAGTACGAACGCAGCCGGCGCATCGATCTTCCGGCAGGCAGCCAGTGGCAGGTGCGCATCCGACGGCTGACCGCGAACGCCAACAGCAGCACCATCGCTGATACCGTCAACGTGCTGTCGATGACCGAGATCATCGATGCCAAGCTGCGCTATCCCAACTGCGCGCTGGCGGCGGTGCAGGTCGACGCCAGCCAGTTCCAGAACATTCCCACGCGCTCGTATCAGCTGTGGGGGCGCATCGTACGCATTCCGTCCAACTATGACCCGCTCACCCGCGTCTACAGCGGAGTGTGGGATGGCACCTTCAAGAGCGGCTGGACCAACAATCCGGCGTGGGTGTTCTTCGACATCGTCACCAACGATCGCTTCGGCCTGGGTCATCGCATCCCGCTGGACTGGGTGGACAAGTGGCGCCTCTACCAGATCGCCCGCTACTGCGACGAACTGGTCAGCGATGGCCAGGGCGGCAGGGAGCCACGATTCACCTGCAGCCTGTACCTGCAGACCCGCGCTGAGGCATACAGGGTGCTGCAGGACATCGCCACCATGTTCCGTGGCATCAGCTTCTATGCAGCCGGCCAGGTCATGGCTTCGGCCGACATGCCCAAGGACCCGCTGCTGACCTACAGCCAGGCCAATGTCATCGAGGGCCGCTTCCACTATGCAGGCAGCAGCCGCACGGCGCGGCACACCGTCGCTCTGGTGTCCTGGATCGATCCGGATGATTTCGGCCGCCAGAAGGTCGAAGTGGTGCAGCACCTGCCGGGTGTCGCCCGCTATGGCATCAACCAGACCGAAGTGACGGCGGTGGGTTGTCATTCGCGTTCGCAGGCGCAGCGCGTGGGCAACCACATCCTGCACACCGAGATGCTGGAAACCGAGACGATCAGCTTCTCGGTGGGGCTGGATGCCCTGGGTTGCATGCCCGGCGACATCATCCAGGTGGCCGACCCGAACCGCGCCGGTCGCCGCAATGCAGGGCGCATCCGCAGCGCGGCTGCGCGCACCTTGGTGCTGGACCAGCCGCCGGAGAAGATTGAAGCCGGTGATACCCTGCGTGCGACGCTGCCCAATGGGCATTCCGAAGCACGTACCGTGCAGTCGGTTGATGGCGAGACGGTCACCGTCACCGCGCCGTGGTCGGCAGTACCGGTCGCGCAGTCGGTCTGGGCACTGGAGTCGCCGGAGCTGGCGCTGCAGCAGTACCGCGTGCTGTCGATCAGTGAAGGCGAAGAACTGACCTACCAGATCACCGCGCTCAAGCATGTGCCGGGCAAGTACGCCGCCATCGACGATGGCACGCGCCTGGAGCAGCCGCCGATCAGCATCGTGCCACCCAGCGTGCAGCCGCCACCCGCGAACGTGCGGATGGCCTCGCATGTGGTCGTCGACCAGGGTATCGCCACTTCCGTACTCACCATCGAGTGGGACGCGGCGGACAAGGCGATTGCCTATGACGTGGAATGGCGTCGTGGTGATCTCAACTGGGTCCGTGCCGGTCGCGTGGGTACGCAGAGCCTGGAAGTGCGCGGCATCTACGCCGGCCAGTACCTGGCCCGGGTTCGTGCGGTCAATGCGCTGGGTGCGGTGTCGCAGCCGATGGTCAGCGCGCTGACGACGATTGAGGGCAAGACCACGCCACCGCCAGCGCTGTCTTCGCTCACGGTCCGCAGTCGCGTCTTCGGCATCGAGCTGGACTGGCAGTTCCCTGTTGGTGCTACCGATACCGAGCGTACCGAGCTCTGGTACAGCACCAGTCCTGACCGTGCAGCGGCCATCAAACTCGGTGACTTTGCCTATCCGCAGGCACGGCACCAGATGAATGGCCTGGCAGCCGGCGCGCGCTTCTGGTTCTGGGGTCGCCTGGTTGATCGCAGCGGCAACATAGGTCCATGGCACCCGGTGGGCGCTGGCGTACTGGGAGAGTCCAGCAGCAACCAGGCGGACTATGACGCCTACTTCGCCGGTCGCATCAACGAAAGTGCACTTGGCCAGCAACTGCAGCAGAAGATCGAGCGCGTCAGCGAGGTGCTGCCGCTGGTCTGGGATGCGGAGGCGACCTATACCGCGGGCCAGACCGTCATCCATGACGGCCGGATCTGGAGCTGGCAGGACACTGCAGCGGGTAACGAAACGCCGCCGGGCACGCATTGGAAGGATGTGGGCGATGCGATCGCCGATGCCGGTGCCATTGTCGGTCGGGTCGATCAGCTTGAGATGGATGTCACCGACGTCGACGGCAAGGTGGCTGCGCAGGGGCAGAAAGTCGATGGCCTGTTCGCCCAGGTCAGCGACCACAGCGCGGGCGAGGAGGACTACAACGTCGGTGAGAACGACGTTACCGCCGGCGCCATCACCGTCTACAGCGTGATGGCCGAAAAGGACGCGGCGCTGGCCAAGCGCGTGGACACGGTTGAAGCCTCCATCGATGGCGTACCTGGCAAGATCGAAGGCGTCAGCGCGGCCGTGCAGCAGGTCTCGCAGGCCGTGGTGAATCTGGATGGCAAGGTCAGCGCGACCTACACGGTCAAGGCGCAGATCAGCAGTGCAGGTCAGATCTACATGGCCGGCATGGGGCTGGGCGTGGAGCAGCAGCCCGATGGCAGTTACCAGAGCCAGATCCTGATGCAGGCCGATCGCTTCGCATTGTTCAACACCAACAGTGGCCAGGTCAGTGCGCCGTTCGTGGTACAGGGCGGGCAGACCTTCATCAATCAGGCATTGATCGGCACTGGCTGGATCCAGAACGCCATGATCGGCGATGTGATCCAGTCCAACGCTATGGGAGCTAATGGCCAGCCCCGATGGAGACTCGACAAGAACGGCACGTTGACGATGAATGGCCCCGAGAACGGCGGCCGCCTGACCATCAATGACAGTGTCATCCACGTTTACGACAGCAGCGGTCGCGTGCGCGTCCGCATGGGGATCTGGTAATGGCAACGGGAATGCAGATTTTCGGCCCGGATGGGCAGATGTGGTTCGACACCAACGATCGTGCCGGAAAGGTGATGGGCGATCTCCATGTAAGCAGTAGTGCCAGCACCTACGTCGGCATGGCCGGAATGGGGGAGCCGTTCGCCATTCTGCCAACGACCTTCTGGGACAGCTGGCAAGATCAGAACGGCAACCAGTTCTCGGCGCCGAACATGGCCAGCATGAGCTTTAGGAGCCAGGGGGCCTACGGAGACTACCTGACCCTCAGTTTTACCTTCATGACCACAACCAGCCCCAATGCCTATCTTTTCTACGGGAGTTTCTGATGACCGTCGGTCTTGAGGTAACAAATGACAGCGGTGTTCCCGTTCTTGTCAATTCACACGCGATGGCTTTCTTTGCCGCTGGCAAAGGTGTTGAATCAATCGGTAGCAACACATCGCCGCTGGGCCAGAGTGGCTCTGTCACCCTGCCTAGGCAGAGCGTGCCGTACCTGGTATTCATCCGCTGCAATAACGGCTCCACGCGTATCGGTACCGGCACCGACGGATTCGGCTGGAACATGGCACAGGGGACGACCAGCTTCGAGTGGTGGGCTTGGGGGCGCGCAGCGCCCAGCACCAACGTCGGCATGCAGGTCTACAACGCCGATGGCTCTGTGCAGTGGGACATGAGCAGCCGTCCGCTGCGAATGGCAGGTCTGGTGGATATGACTGGGGCAAGACCTCCGGTGCCCAGCGAGATGTCCAACGAGAATATTCTGACAGGTGATCTGGTAAACGGGCCCGGCGATAATCTTGCCTACCTGCTGTCCGATATCGGCATGTGCCACGATGTCTACGCCATGCCGAGTGGCAATCCCACCATTCGCACCAACATGCGCTACATGGCCGCTATAAGCACGCCGACCGCATCGCAACTGCGCATCAACTTCTGCAGGCGGGCCGCCAATCGTCAGCGGTCCCTGAGCGGAGCGTCCTATCAGACCTTCGCCTCGCGTCTGCCGAGCTTTGTACTGGCAGCCTATACCTACTGATGTGCCTCAATCGACCCGGGCGGCCATTTGAGCCGCCCGGCCCCTTCCCGTAGACTGCGCCCCTTCCACGCTCCCCGACGACGCACTGCAGTGATCACGCCACCCTGACCCTTGCCGCCCCTCGGCAGCCGGCCCAACCGGCTCAGGAACCCGCGTCTTTCCACTGCAGCGCCACGTGGCCCAGCCCACGTGTGCGCGGAGTTTTCCCATGCAAACGTCTTATCCCCTGCGCCAGCAATGGCTCGGCAACCTCCGTGGTGATCTGCTGTCCGGCACCGTCGTCGCCCTGGCACTGATTCCCGAAGCCATCGCGTTCTCGTTGATCGCCGGCGTCGACCCCAAGGTCGGCCTGTATGCTGCTTTCTCCATTGCCGTCATCACCGCGATTGCAGGCGGCCGCCCCGGCATGATCTCTGCCGCCACCGGCGCGATGGCCCTGGTGATGGTCGACCTGGTCAAGGACCACGGCCTGCAGTACCTGTTTGCCGCCAGCATCCTGGCCGGCCTGCTGCAGGTGCTGGCCGGCGTGTTCAAGCTGGGCTCGCTGATGCGCTTCGTCTCGCGCTCGGTCATCACCGGCTTCGTCAACGCGTTGGCCATCCTGATCTTCCTGGCCCAGATGCCCGAGCTGATCGGCCGCGGCCCCACCGTGTATGTGCTGTGCACCGCCGCGTTGGCGATCATCTACCTGCTGCCGCGCATCAACCGCGCAGTGCCTTCGCCGCTGGTGGCGATCGTCGTGCTCACCGCCGTGGTCATCGGCTTCGGCATCGATGTACGCAGCGTGGGCGACATGGGCCAGCTGCCCGACAGCCTGCCGTACTTCCTCATCCCCGATGTGCCCTTCACCTGGGAAACGCTGCGCATCCTGCTGCCGGTGTCAGCCACGCTGGCGGTGGTCGGCCTGCTCGAATCGATGATGACCCTGCAGATTGTCGAGGACATCACCGAGACGCCCAGTGAGCGCAACCGCGAGTGCGTCGGCCAGGGCCTGGCCAACACGGTCACCGGTTTCCTCGGTGGCATGGCCGGCTGCGCGATGATCGGTCAGTCGGTGATCAACGTGACCTCCGGCGGTCGAGGCCGCCTGTCCTGCCTGGTGGCCGGCGTGCTGCTGCTGGTGCTGGTGGTATACGGCAGCGACCTGGTGCGGCAGATCCCGATGGCCGCACTGGTGGCGGTGATGATCATGGTCAGCATCGGCACCTTCAGCTGGCGCTCGCTGCGCGACCTGCGCACGCATCCGCGCAGCTCGTCGGCAGTGATGCTGCTGACCGTGGTGGTCACCGTGGCCACCCACGACCTGGCCAAGGGTGTGCTCAGCGGCGTGCTGTTGTCTGCCCTGTTCTTCGCCCGCAAGGTGAGCCGCATGCTCGACGTGCAACGCGAAGACGTTGCAGACATGGACATGCAGGTCTACCGCGTGCGCGGCCAGGTATTCTTCGCCTCCGCCGGACAGCTGGGTGCGGCGTTCGACTACCAGCACGTGGCGCCGAAGGTACAGATCGACCTGCGGGAGGCCCACCTGTGGGACCTGACTGCCGTCGCCGCGCTGCAACGCGCGCAGGAAAAGCTGGCCGCGCATGGCGCCGAAGTCAGTGTTGTCGGCCTCAACGCGGCCAGCCAGACGCTGATCGAACAGGTGGGGGACAGGGGCGGTGCGTACTGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP040429|279577:297214|294834_295545_+|WP_139784987.1|DBSCAN-SWA
MTVGLEVTNDSGVPVLVNSHAMAFFAAGKGVESIGSNTSPLGQSGSVTLPRQSVPYLVFIRCNNGSTRIGTGTDGFGWNMAQGTTSFEWWAWGRAAPSTNVGMQVYNADGSVQWDMSSRPLRMAGLVDMTGARPPVPSEMSNENILTGDLVNGPGDNLAYLLSDIGMCHDVYAMPSGNPTIRTNMRYMAAISTPTASQLRINFCRRAANRQRSLSGASYQTFASRLPSFVLAAYTY
>NZ_CP040429|279577:297214|279577_280090_+|WP_154879091.1|head,tail|DBSCAN-SWA
MPLLTLEQCRMHCRIDGDYDDAILDDLLAAATDAASAYLRRALFADQAALDLALDQLPQDMAAAVTGHEAAVAAANAETNAAKAKAMRDVADRRLAAATERSAQLLQGLPANDSIRAAVRLLLGHLYAHREAVVVSTHALDIPVGAAAIAMELPFGIAALLDPYRLAATP
>NZ_CP040429|279577:297214|283930_285079_+|WP_154879098.1|DBSCAN-SWA
MDLQQIDLDTLQPNGKRGETQRPAFTKINQNFKEVALAVDAVPEAVARAVSGRNRLINGNFDCWQRGTSFNTSGRYTADRWFLQMQGIADPVFRRNPTAMGDNNFPRSKYTLSVSSSGNTDAEKHFFVFEQRVEDVRTFADTPSTVSFLVFNAGAGGRRIALEFAQTFGATGSAPVLAVAPEIFELAPGLNRIRKTVTLPSISGKTLSDEGAVVMCVWVSAGTQFAKRTAGLGAQHGQVYFGEFQWERGATATAFEWRSLDEEVQRCRRYYQADATGSYFDGGVRFNAGVGLIRGDNKVYLIYPFSQRMRTIPTVGFSNLPQWRLLTGSGATSLTALNAVEVSSTRMTIIGSLNEAAAGQAGILQSADSADAGTGISLDAEI
>NZ_CP040429|279577:297214|291020_294509_+|WP_154879110.1|DBSCAN-SWA
MNQIIHSAQRERSAPIPTLAGAKKGASNARTPVETPDSLHSMAVARIIDLASEGEIRGLVAGKQSIYLDQVPIENPDGTLNFSGVDVQTRSGTQDQEHISGFPSIENEVGVNVELRSDAPVVRTVSGADLSAVRIRFAVPALQKTNTENGDTEGYRIMYAVDLSTDGGPFSTVLNDAFSGKTTSQYERSRRIDLPAGSQWQVRIRRLTANANSSTIADTVNVLSMTEIIDAKLRYPNCALAAVQVDASQFQNIPTRSYQLWGRIVRIPSNYDPLTRVYSGVWDGTFKSGWTNNPAWVFFDIVTNDRFGLGHRIPLDWVDKWRLYQIARYCDELVSDGQGGREPRFTCSLYLQTRAEAYRVLQDIATMFRGISFYAAGQVMASADMPKDPLLTYSQANVIEGRFHYAGSSRTARHTVALVSWIDPDDFGRQKVEVVQHLPGVARYGINQTEVTAVGCHSRSQAQRVGNHILHTEMLETETISFSVGLDALGCMPGDIIQVADPNRAGRRNAGRIRSAAARTLVLDQPPEKIEAGDTLRATLPNGHSEARTVQSVDGETVTVTAPWSAVPVAQSVWALESPELALQQYRVLSISEGEELTYQITALKHVPGKYAAIDDGTRLEQPPISIVPPSVQPPPANVRMASHVVVDQGIATSVLTIEWDAADKAIAYDVEWRRGDLNWVRAGRVGTQSLEVRGIYAGQYLARVRAVNALGAVSQPMVSALTTIEGKTTPPPALSSLTVRSRVFGIELDWQFPVGATDTERTELWYSTSPDRAAAIKLGDFAYPQARHQMNGLAAGARFWFWGRLVDRSGNIGPWHPVGAGVLGESSSNQADYDAYFAGRINESALGQQLQQKIERVSEVLPLVWDAEATYTAGQTVIHDGRIWSWQDTAAGNETPPGTHWKDVGDAIADAGAIVGRVDQLEMDVTDVDGKVAAQGQKVDGLFAQVSDHSAGEEDYNVGENDVTAGAITVYSVMAEKDAALAKRVDTVEASIDGVPGKIEGVSAAVQQVSQAVVNLDGKVSATYTVKAQISSAGQIYMAGMGLGVEQQPDGSYQSQILMQADRFALFNTNSGQVSAPFVVQGGQTFINQALIGTGWIQNAMIGDVIQSNAMGANGQPRWRLDKNGTLTMNGPENGGRLTINDSVIHVYDSSGRVRVRMGIW
>NZ_CP040429|279577:297214|295753_297214_+|WP_154879112.1|DBSCAN-SWA
MQTSYPLRQQWLGNLRGDLLSGTVVALALIPEAIAFSLIAGVDPKVGLYAAFSIAVITAIAGGRPGMISAATGAMALVMVDLVKDHGLQYLFAASILAGLLQVLAGVFKLGSLMRFVSRSVITGFVNALAILIFLAQMPELIGRGPTVYVLCTAALAIIYLLPRINRAVPSPLVAIVVLTAVVIGFGIDVRSVGDMGQLPDSLPYFLIPDVPFTWETLRILLPVSATLAVVGLLESMMTLQIVEDITETPSERNRECVGQGLANTVTGFLGGMAGCAMIGQSVINVTSGGRGRLSCLVAGVLLLVLVVYGSDLVRQIPMAALVAVMIMVSIGTFSWRSLRDLRTHPRSSSAVMLLTVVVTVATHDLAKGVLSGVLLSALFFARKVSRMLDVQREDVADMDMQVYRVRGQVFFASAGQLGAAFDYQHVAPKVQIDLREAHLWDLTAVAALQRAQEKLAAHGAEVSVVGLNAASQTLIEQVGDRGGAY
>NZ_CP040429|279577:297214|286338_287577_+|WP_154879102.1|DBSCAN-SWA
MTRKIIDLDTIQANGKRGETQRPAFTKINENFAEVYGALGSVATIVEDVEQLKTEIQAEADQAKVEVQSAIAALPSAVDNAIHGRIPAKNRLINGNFDFWTRGTPVMQTGYGPDRWFVQIGSMVDAGLFANNNVPGDGVFGDARLSMGANSTGNSDAFGHYFVFEQRVENVRTFAGVLSTVSFTVYNSGAAGRKIAVEFLQNFGTGGSETALGLDAEVFSLDVGINRISKTTTLPSVSGKTVASTNHYAAVAVWLSSGSGFDVRNAALGAQSGQLFFGQFQWEEGGTATGYDTRLLSHEAALCGWYAQRIDINAGDAFSVCTALGQFDCVGQLAFQPMRSKPSARTLGNGVNMTGFGINGGNAPGSSFNVIPVSVSSAAITAGVATGGMSPNASGYVAPKTGGISIIFEAEI
>NZ_CP040429|279577:297214|288939_289635_+|WP_025875707.1|tail|DBSCAN-SWA
MITADAQQLEPGGRITVFELDASSFGADQLFFHAHLQSGVIIWQGQEYGPWPIEASGFERTSDQPPNPKLRVSNIDGRITAMCLLFDDLVGARVIRRQTLAKYLDAANFEEGNSSADPAEHFPDEVWFIERKVGEDKQTVEFELTTAIDLNGEQLPGRQIIAGMCGWLVRGGYRGPYCGYNGPAVADGDDVATDDPARDQCGGRVRSCKMRFGQDKPLPYGGFPAAGLLRS
>NZ_CP040429|279577:297214|285148_286300_+|WP_154879100.1|DBSCAN-SWA
MSRRIIDLDSIQPNGKRGETQRPAFTKINENFAEVYDALAAVEKLPETVDHAISGRLPGRNLFINGGLQFWQRRTSGRVGSGSGTLGAETFFADRFSNSALSCSHDIQRVPYEGQLGYPEDTRAILVCTVSGAVANSGAWMGQRIEGVRSASGAVTISVWANSDVAGRKVGVRVIQDFGTGGTPSPQVSTEAGVLTLSTGASRQSLTVTLPSTKGKKLGANGNDHIYVVFDLCAGGYGGALAGQNGSFGFSQFQVEPGRNATNFDWRPPGVELALCQRYYEKSYNLDVPPNTPHNEGREAFSLNNPGVAHYQSVRFLVAKRAHPYVMIISADTTQQDGHIAEDNISRVPCVVNYASPSSYEVSWSNNPGRWGGWWHWWADAEF
>NZ_CP040429|279577:297214|280886_281546_+|WP_025875728.1|tail|DBSCAN-SWA
MALKLPKGTQFGFAPVVSTAIATSAISKAAPALASVAANSVDTGDVVVIELPGWPALNNRATRAGAEATGSVELLGIDTTDNVLFPATSGAGVLRKAGAFVDLDQQGDPTTAGGEQQYWSGTLLEDPTGRQVQMPTFKNAKTITLPLFYDPKKPWYSALKNVDAKGEPVILRAKLVGGDVLYWYGYLSYNGDPTMAANTPMGTTATFTALADSILVEGA
>NZ_CP040429|279577:297214|289697_290438_+|WP_154879106.1|DBSCAN-SWA
MQPTTLQAIQAHAVAEYPRECCGLIVAIEGHEHYLPCRNLAGTPSEHFRLPAEDYAVAEDKGEVLALVHSHPDAAATPSDADRVMCEHSGLTWHIVSVGQVDGEAPECGDLQTIQPNGYVAPLVGRQFTHGVLDCYSLVRDFHARELGISLSDYTRDDDWWDKGQDLYSLERLHAEGFDLIEGEPQRGDMILMQIRSPVTNHAGVYLGDGQMLHHLHGRLSETVPYGGMWAERTRCIVRHREVRHD
>NZ_CP040429|279577:297214|281904_282162_+|WP_032978329.1|DBSCAN-SWA
MQLGLKAKHFPPPRVELWPECVLPIELFSRVATQWRVGAGGPIGLDYNVVYRELEREALDGDQYDEVMAAIRVIERAALEQMQQE
>NZ_CP040429|279577:297214|283592_283922_+|WP_025875719.1|tail|DBSCAN-SWA
MTDTFTWAATSQSTGTTTATVKRARFGDGYAQAAPDGLNARLRSYQLQFVGNRSTINEIVAFLDGHVGQSFFWRGPLGTGLYGCDTYTDSHLGGSVFSITATFEQTYQP
>NZ_CP040429|279577:297214|281545_281854_+|WP_032978191.1|DBSCAN-SWA
MFQVKAPESFKSTLTIIGHGREQKLNLTYRHLPVADYAQLLERLGDDTLSVAQAILDIVVDWDADVPLDTAGVELALQQQAGLDGAIIGGYTQALQVARKGN
>NZ_CP040429|279577:297214|287659_288790_+|WP_154879104.1|DBSCAN-SWA
MKIIDLDTIQANGKRGETQRPAFTKVNDNFADVYAGLDGVQTAVDGLESRMAGRNRLINGDFRVWQRGTAFSASTGARPTADRWLVNAHATTLSASRDDIAAGGGAAGRLIAGSRHLLKLVVESVAGADSMALVQQRIEDVRTFAGKRVTVSFKARATVDNFKVGLEFQQSFGAGGSTARDSIGGGVTLDTMWRWHQLTVDVPGIAGQTLGADSYLQLSLWLDAGANFAGRAFGAGQKSGVVYLAEMQVEEGEIATDFDRRPEALELLLCQRYYETVDVNRILGITYTANGDSRACIPFKVRKRVAPRITSPSTALNLVGFGSEGSLINFNGGDPGWQSTVDAAVLSSMSNNMQQCGPVVVWSTTSQVLVHADAEL
>NZ_CP040429|279577:297214|280451_280808_+|WP_025875730.1|DBSCAN-SWA
MSYEPKLQQLLGGLLQGRLYPDVPPDRVTYPCAVYQQVGGQALWFNEGSIPDQKHARVQLTVWADTRAQANTLIRDIEDQVCAGLPKSESFGAAIAVHEPALRKYGARLDFGLWYANP
>NZ_CP040429|279577:297214|282237_283596_+|WP_154879095.1|tail|DBSCAN-SWA
MSTTSLGSTRATVDASNALETAMQAARRSMTEMTGTTQEFQRQLEKINTVQQAFNAVLTTSASLVTALSTQLTALNTQMQAVAKSATAAAGGDAGKAAKAEEKADKDDMGLAGIRKGLGGALGDYIGKTENTATAAKKAFGKAFTGADEALRSFVTTGKSKYKELAQSILSDLKMIAAQQALVWGARKIAGMMGVDLAPKDAATDAAAAAAGVAAPKDAKAGDAKAGDTKGGKDDKDAKGFSGFRKGFGSALGEYMEKTENSAKTTQDAFSKAFTGAEAALQSFVKTGKSNYKELAKSIIADLKMIAIQQAIVWGVKKITGMLGYGTGVEANAKGGVYQSPSLSAYSGGIYNTPQLFAFAKGAGVFGEAGPEAIMPLQRGPDGRLGVAAHGAGGGVGVNIRIDNNGGKEVTSNESMLQQFGNEIGQFVERKYRDLQMRDMKAGGVLSRSAAR
>NZ_CP040429|279577:297214|290430_291024_+|WP_154879108.1|tail|DBSCAN-SWA
MTDRLRTIRLYGKLGARFGRKFRLAVNSPAEAVHALCVMLPGFQQYLMGAKSKGMEFAVFNGRQNLSRDQLHDPPGQDDIRIAPVMVGSKRGGVLQTIIGIVLIVVGSYTSWAGGAALVSTGVSMVVGGITQMLSPQPKGLGAKDTPENAPSYSMNGTVNTQAQGNPVPVAYGGHDKKGMFIGSAVISGGILAEDQF
>NZ_CP040429|279577:297214|294508_294835_+|WP_032951856.1|DBSCAN-SWA
MATGMQIFGPDGQMWFDTNDRAGKVMGDLHVSSSASTYVGMAGMGEPFAILPTTFWDSWQDQNGNQFSAPNMASMSFRSQGAYGDYLTLSFTFMTTTSPNAYLFYGSF
>NZ_CP040429|279577:297214|280086_280437_+|WP_154879093.1|head,tail|DBSCAN-SWA
MNAGHFNRRIRIERQDGRVDAWGQPLDAWVSVADLWAAIPLERADAVQRVKLDSGLSAAIRRQRFQVRLAPAQRAGIGIGMRIVHDGHTFDITGVVPDLGTRHTAVLFTEQLAATA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_154879091.1|279577_280090_+|head,tail	phage gp6-like head-tail connector protein	Q6JIM5	Burkholderia_virus	3.3e-05	29.7
WP_154879093.1|280086_280437_+|head,tail	head-tail adaptor protein	NA	NA	NA	NA
WP_025875730.1|280451_280808_+	DUF3168 domain-containing protein	NA	NA	NA	NA
WP_025875728.1|280886_281546_+|tail	tail protein	C4ML12	Xanthomonas_virus	5.8e-63	56.2
WP_032978191.1|281545_281854_+	hypothetical protein	NA	NA	NA	NA
WP_032978329.1|281904_282162_+	DUF1799 domain-containing protein	Q7Y5K1	Xanthomonas_virus	5.4e-09	37.7
WP_154879095.1|282237_283596_+|tail	phage tail protein	K7PM62	Enterobacteria_phage	1.0e-21	32.0
WP_025875719.1|283592_283922_+|tail	phage tail protein	A0A2R3UA73	Siphoviridae_environmental_samples	4.1e-25	50.9
WP_154879098.1|283930_285079_+	hypothetical protein	NA	NA	NA	NA
WP_154879100.1|285148_286300_+	hypothetical protein	Q2PGB9	Xanthomonas_virus	2.2e-33	31.7
WP_154879102.1|286338_287577_+	hypothetical protein	NA	NA	NA	NA
WP_154879104.1|287659_288790_+	hypothetical protein	A0A0H4IPB2	Stenotrophomonas_phage	9.9e-71	49.7
WP_025875707.1|288939_289635_+|tail	phage minor tail protein L	A0A2R3UA90	Siphoviridae_environmental_samples	2.8e-92	67.5
WP_154879106.1|289697_290438_+	peptidase P60	A0A2R3UAR4	Siphoviridae_environmental_samples	5.3e-81	58.8
WP_154879108.1|290430_291024_+|tail	tail assembly protein	W0LI27	Edwardsiella_phage	1.9e-49	53.5
WP_154879110.1|291020_294509_+	DUF1983 domain-containing protein	A0A2R3UA88	Siphoviridae_environmental_samples	0.0e+00	59.3
WP_032951856.1|294508_294835_+	hypothetical protein	NA	NA	NA	NA
WP_139784987.1|294834_295545_+	hypothetical protein	NA	NA	NA	NA
WP_154879112.1|295753_297214_+	sodium-independent anion transporter	A0A2H4J153	uncultured_Caudovirales_phage	2.0e-156	63.8

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP040429|622625:631603|DBSCAN-SWA
AGTGCCCACATGGCTTGTCACCGGCGGCGCCGGATTCATTGGCGGTAACTTCGTTCTCGAGGCCGTTGCACGCGGCGTCAAGGTCATCAACCTCGATGTGCTGACCTACGCCGGCAACCTGAAGACCCTGTCCAGCCTGGACGGCAATCCCAACCACGTGTTCGTCCAAGGTGACATCGGCGACAGCGCGCTGGTTTCACGCCTGCTGGCCGAGCACCAGCCCGATGCGGTGCTGAACTTCGCGGCCGAAAGCCACGTCGACCGTTCCATCGACGGCCCAGGCGCGTTCATCCAGACCAATGTCGTCGGCACTCTCGGCCTGCTCGAGGCCGTGCGCGATTACTGGAAGGCGCTGCCGGCCGATCAGGGCGCGGCCTTCCGCTTCCTGCATGTCTCCACCGACGAGGTGTACGGCACCCTGGGCGAGACCGGCAAGTTCAGCGAAACCACGCCGTATGCCCCGAATTCGCCGTACTCGGCGTCGAAAGCGGCTTCGGACCACCTGGTCCGCGCCTTCCACCATACGTACGGGCTGCCGGTGCTGACCACCAACTGCTCCAACAACTACGGTCCGTACCACTTCCCGGAGAAGCTGATCCCGCTGGTGATCGCCAAGGCGCTGGCCGGTGAGCCGCTGCCGGTGTACGGCGATGGCAAGCAGGTGCGTGATTGGCTGTTCGTGTCCGACCATTGCGAAGCGATCCGTACCGTGCTGACCAAGGGCCAGGTGGGCGAGACCTACAACGTCGGCGGCAACTCCGAAAAGCAGAACATCGAAGTGGTGCAGGCGATCTGCGCGCTGCTGGACCAGCGCCGCCCGCGTGCGGACGGCCAGCCGCGCAGCAGCCAGATCACCTACGTTGCCGACCGCCCGGGCCATGACCGCCGTTACGCGATCGATGCCTCCAAGCTGAAGAACGATCTGGGCTGGGAGCCGGCCTACACCTTTGAACAGGGCATCGGCTTCACCGTCGACTGGTACCTGGACAACCAGGAATGGGTGAACGGCGTGCTCGACGGCAGCTACCGCCTGCAGCGCATCGGCACCGCGGCCTGAACCAAGGACACGACATGACCCAACGCAAGGGCATCATTCTCGCCGGCGGTTCCGGCACCCGGCTGTATCCGATCACCAAGGGCGTCAGCAAGCAGCTGCTGCCGGTGTATGACAAGCCGATGATCTATTACCCGCTCAGCGTGCTGATGCTGGCGGGCATCCGTGAAGTGCTGATCATCAATACCCCGCACGAACAGGCCTTGTTCCAGCAGTTGCTGGGCGATGGCTCGCAGTGGGGCATGGACATCCAGTACGCCGTGCAGCCAAGTCCCGATGGCCTGGCCCAGGCGTACCTGATCGGCCGCGATTTCGTGGCCGGCAAGCCGAGCTGCCTGGTGTTGGGTGACAACATCTTCCACGGCCATGGCCTGCGCGAGGTGCTGCGCAATGCCGATCAGCGCGACCACGGCGCGACGGTGTTCGGCTACTGGGTCAATGATCCGGAGCGTTACGGCGTTGCCGAGTTCGACAAGTCCGGAAAGGTGGTCGACCTGGTGGAGAAGCCGGAGAACCCGCGTTCCAACTATGCCGTGACCGGCCTGTATTTCTACGACGGCAATGCCAGCCACCATGCGGCCGAGCTGAAGCCGTCGCCGCGCGGCGAGCTGGAGATCACTGATCTGAACCAGCGCTACCTGCGTGAAGGCAACCTGCATCTGGAGGCGCTCGGCCGCGGCTACGCGTGGCTGGATACGGGTACCCACCAGTCGCTGCTGGAAGCGTCCAACTTCATCGAGACGATCCAGACCCGCCAGGGCCTGCAGGTCTGCTGCCCCGAGGAAATCGCCTTCGGCCAAGGCTGGATCAGCGCCGAGCAGTTGGAAGCGCTGGCTGCACCGCTGATCAAGAATGGCTACGGCCAGTACCTGCACAAGCTCGCCCTGCGTGGAGTCGTTCCGTGAAAGTGATTGAAACCAAGTTGCCCGGCTGCGTGGTGATCGAGCCGGCCGTGTTCGGCGATGCCCGTGGTTATTTCTTCGAAACCTGGAATGCCGAGCGCTTCGCAGCGCTGGGCCTGCCGGATCGCTTCGTGCAGAGCAATGTTTCCACCTCGGCGCAGGGCGTGCTGCGCGGCCTGCATTACCAGTGGCCGCGCCCGCAGGGCAAGCTGGTCAGCGTGCTGGAAGGCGAGGTCTACGACGTGGCTGTGGACATCCGCCGCGGTTCGCCGACCTTCGGTCAGTGGGAAGCGGTGGTGCTGAGCGCGGAAAACAAGAAGCAGTTCTGGATTCCGGAAGGTTTCGCGCATGGTTTCGCGGTGCTGTCCGAACGCGCGGTGTTCAGTTACCTGTGCACCGAGGTCTACCTCAAGGACTTCGATGCCGGCGTGCGCTGGAATGACGCCGATATCGGCGTGGACTGGCCGGTCAGTGCACCGACGCTGTCGGCCAAGGACGAGAACGCTCCCTTCCTGAAGGACATTGCTGAAGACCGCCTGCCGGTCTACGTGCCATGACCGTTCTGGTGTTCGGCGGCAACGGCCAGGTCGGCCAGGAGCTGCTGCGCGCGCTGGCACCGCTGGGCAAGGTGGTTGCGACCACCCGCAGCGGCGTCCTGCCCGATGGCAGCGCCTGCGAAACCGCCGATTTCGGCCAGCCTGACAGCCTGCCGGCGCTGCTTGACCGGCTGCAACCGTCGATCGTGGTCAATGCGGCCGCCTACACCGCCGTCGACCGTGCCGAACAGGAGGTCGACGCCGCCTTTGCGGCCAACGCGCAGGCGCCGGGCGTGATCGCGCGCTGGTGTGCGGCGCATGGGGTGCCGTTCGTGCATTACTCCACCGACTATGTGTTCGATGGTCAGGGCACGGCCCCGTACCGCGAGGATGAACCGACCGCGCCGCTGGGGGTCTATGGCACCAGCAAGCGTGATGGCGAAGACGCCGTGCGCGCTGCCGGCGGCCGTCATCTGATCTTCCGCACGGCATGGGTGTATGCCTCGCACGGCGCAAACTTCCTGCGCACGATGCTGCGGGTGGGCGCTGAGCGCGATCAGCTGCGTGTGGTGGCCGACCAGATCGGCACGCCGACGCCGGCGGCATTGATCGCGGATGTCACCGTGCAGGCGCTGCAGCATCCGGGCGCGCTGTCGGGAACGTGGCATCTGACGGCGTCGGGCCAGACCAGCTGGCATGGTTTTGCCGAAGCGATTTTCGCCGAAGCACTGGCGACGGGCGTGCTGGCCAAGGTGCCGTCGGTTGAAGCCATCCCCAGTTCCGAATACCCGACCCCGGCCAAGCGTCCCGCATGGTCGGTGCTCGACAACCGCAAGCTGCAGCAGGATTTTGGCATCGCGCTGCCAACGTGGCAGGACGGCCTGAAGCGGGTCATGGCTGAACTGGCCCGCTGACGGTAGCGCCGGGCCATGCCCGGCGGATGCACATTGCCGCTGCGCTCGCCGGCCATGGGCCGGCGCTACCCAGAATGCAGCGGGTTCCGGGTCAACTCCGCCCGTACGTATCCTCGAACCGCACGATGTCATCCTCGCCGAGGTAACTGCCGGACTGCACCTCGATCAGTTCCAGCGGCAGCTTGCCGGGGTTGCGCAGGCGATGGGTCACCCCCAGCGGGATGTAGGTGCTCTGGTTTTCGCTCAGCAGGATCACCTCGTCGCCACGGGTGACTTCGGCGGTGCCGCTGACCACGATCCAGTGCTCGGCACGGTGGTGGTGCATCTGCAGGCTCAGCGTACCGCCGGGCTTGACCGTGATCCGCTTGACCTGGAAACGCTCGCCGTTGTCGATTGAATCGTAGGCTCCCCACGGGCGGTAGACCTTGCGGTGCCAGGTCGCTTCGCTGCGGCCGTCAGCCTTCAGCTTCGCCACCACCGTCTTGACCTCCTGCATGCGGTCGGCCTTGCCGACCAGCACCGCGTCGTCGGTCTCGACCACGATCACATCATCCAGCCCGACCATCGCCACCAGGCGTTGGCCGTAGGCATAGGTGTTGCGGCAGTCGATGGCGATCACATCCCCCTGGTGCGCATTGCCATCGCCGTCCTGCTGCGATACATCGCGCAGTGCGGTCCAGGAGCCGACATCGTTCCAGCCTGCATCCAGCGGCACCACCACTGCATCGGCGGTCTTTTCCATCACGGCGTAATCGATCGAATCGGACGGCACGGCAGTGAACGCGTCCCTGTCCAACCGGGTGAAATCGGCATCGCGGCGTGCGCTCTGCCATGCGTCGCGGCAGGCCGACAACATGGCCGGCTGCAGGCGTTCCAGCTCCTGCAGGTAACGCGAGGCCTTGAACAGGAACATGCCGCTGTTCCAGTAGTACTGGCCGCTGGCCACGTAGCCGGTGGCGGTGTCCAGATCGGGCTTTTCGACGAAACGTTCAACCGCGCGCACGCCTTGGCCGTCGGCGGCCTTGATGTAGCCGTAGCCGGTTTCTGGGCCGGTCGGCACGATACCGAAAGTGACCAGCTTGCCGGCTTCAGCGGCGCCGGCAGCAGCCTGCACCGCAGCGCGGAACGCGGCTTCGTCGGTAATCACGTGGTCGGAGGGCAGTACCAGCAGCAGTGCATCGTTGCCATCGCGGGTCGCCTCAAGCGCGGCCACGGCAATGGCCGGGGCGGTGTTGCGGCCGACCGGCTCAAGGATGATCGCGGCCGGCTCGGCGCCGACCTGCTGCAGTTGTTCGGCCGCAACGAAGCGATGTTCCTCATTGGCAATGACCAGCGGGCCACGGCTGGCAATGGGCGCCACGCGCCGCCAGGTCGCCTGCAGCATCGTCAGCTCACCGGCCAAGGGCAGGAACTGCTTGGGATACGCTTCGCGCGAGAGCGGCCACAGACGGGTGCCGGAACCACCGGAGAGGATCACGGGCTGGACGGTGTTCATCGGAACATCTCCGCTCAGGCCTTCAACAGCGTGGCGATTTCGTCGGTGCGTGCCTGCATCAGCGCCGCATCCCCACGCGATTCCACGTTCAAGCGCAGCAGCGGCTCGGTGTTGGAACTGCGCAGGTTGAAGCGCCAGTCGCCGAAGTCGGCACTGATGCCATCGGTATGGTCCAGCGCCGGCGACTGCGCGGCGAAGTATTCCATCACGCGGGCCACGGACGCCTTCGCATCGCTGACCTTGAAGTTGATTTCGCCGCTGCACGGATAGGCGGCCATGCGGTCTTCAACCCAGTCGGCCAGCGAACGGCCGCTTTCGGAAATGAGCTGGGCGATCAGCAGCCAGGGGATCATGCCCGAGTCGGCATAGGCGAATTCGCGGAAGTAGTGATGGGCACTCATTTCGCCGCCATACACCGCGTCCTCTGCGCGCATCTTCTCCTTGATGAAGGCATGGCCGCTCTTGCACAGCACCGGCACACCACCCGCCTGTTCGACCATCTCCACGGTGTTCCAGACCAGGCGTGGGTCATGCACGATCTTGCCACCCGGGTTACGGTCCAGCGCCGCCTTGGCCAGCAGGCCGACGAGGTAATAGCCCTCGATGAAGCGCCCGTTGTGGTCGAAAAAGAAGCAGCGATCGAAATCGCCGTCCCAGGCAATGCCGAAGTCGGCGCCGTGCTCGCGGACCGCCTCGGCCGTGGCAGCGCGGTTCTCCTGCAGCAGCGGATTGGGAATGCCGTTGGGGAAGCTGCCATCGGGTTCGTGGCAGATGCGGATGAACTCGAACGGCAGGTGCGGTGAGAGCAGGTCGACGATGACGCCGGCGCCCCCATTGCCTGCGTTGACCACCAGCTTGAGGGGCTTGAGCTTGGTGCTGTCCACATAGGACAGCAGATGCTGGATGTAGGCGCTCTTGTCGTGCTCGCTGCGTTGGCCTGCGGTCGGCGGCTGCGGTGTTGCGCTGTCGGCCGCCACGGCATCGGAGATCGCGAACAGGCCGGTATCGGAACTGATCGGCCGGGCGTTCTCCTTGACCAGCTTCATGCCGTTGTAGTCCATCGGGTTGTGGCTGGCGGTAACCATCACACCGCCCGCTGCACCGCGATGGTCGGTCTGGAAATAGACTTCCTCGGTGCCGCACAGGCCGATGTCGATCACTTCCCGGCCCGCGCCGCGCAGGCCGGCTGCCAGGGCATCCTGCAGCGCCGGACTGGTCAGGCGGACGTCGTGCCCCACCACCACTGGCCCGGGTGACAACTGATTGGCCAAGGCCACGCCGATCCGCCGGGCGAGGTCTTCGTTCAGTTCTTCCGGCACGCGGCCGCGGATGTCATAAGCCTTGAAGGCGGGCAGGGGCATCGCTGGAATCCTTTGTCAGATCAGTTGGCTAGTGTAATCCCAGCCTTGTATGGGAATCGTTTCCATAGACCCAACGCTGCCTGACCGCCGAGTGGTCACGTGTGGGTGGCCCTGCGTCTGCCTGCCGCGCGTTTGGCCGGCGCGCCGGGCAGGGGAGACAGCAGGGCCTCAAGGTCGGCTGCGTCGAAACGTGGGCCTGTGCCGCCATTGCCCTCCAGGATCGCGTCGGCCAGGTCGGCCTTGCGCTGCTGCAGCTCGGCGATCCGTTCCTCGACGCTGCCGGCGGTGATCAGCTTGTAGACGAACACCGGCTGGTCCTGGCCGATGCGATGGGCACGGTCGGTGGCCTGGTTCTCGGCGGCCGGATTCCACCAGGGATCGAAGTGGATGACGGTGTCGGCAGCGGTCAGGTTCAGGCCCACGCCACCGGCCTTCAGGCTGATCAGGAACACGGGAACCTCGCCCTGCATGAAGCGCTGCACGGGCGTGACCCGGTCCTGGGTATCGCCGGTGAGCTGCACGTAGGGCAGGCTGAGTTCCCGCAGGGCCTGGCCGATCAACGCCAGCATGCCGGTGAACTGCGAGAACAGCAGGATGCGCCGCCCTTCCTCGACCATGGCAGGCAACATCTCGCGCAGCAGGTCCAGCTTGGCCGAACCGGCAGCGCGCGCGGGTGTCTCGCCTGGCAGCAGGCGCGGATCGCAGCAGACCTGGCGCAGCTTCAGCAACGCGTCCAGTACCACGATGTGATTGCGCGCCAGCCCGCTGCCGTTGATCGCATCGCGGACCTGCTTTTCCATCGCCACGCGCACGGCTTCGTACAGATCGCGCTGGGCGCCTTCCATTGCCACGGTGCGGGTGATGACCGTCTTCGGTGGAAGCTCGGAAGCGACCTGGTCCTTGCGCCGGCGCAGGATGAAAGGTCGCAGCCGCTGGGCCAGCAGCTGAGCATGCCGCTGGTCGCTGCCGCGTTCGATGGGATGGCGCCAGTGCTGGTTGAACTGTTTTTCGCTGCCGAGCAGGCCGGGCAGCAGGAAGTCGAACTGCGTCCACAGCTCGCCCAGATGGTTCTCCAGCGGGGTACCGGTCAGGCACAGCCGATGCCGCGCCTGCAGCGTGCGCAGCGTGGCCGCCGCGCGCGATCTGGGATTCTTCACCTGCTGTGCCTCGTCCAGGATCAGCAGGTGATAGGAATGGGCCTGCAGCGCCGGTTCGTCGCGCCAGAGCAGGGGATAGGTGGTGAGTATCAGATCATGGGCGGCAATGGCGTCGAACTGCGTGTCACGTGCGGGGCCGTGCAGGGTCAGTACACGCAGATCCGGGGTGAAGCGCGCCGCCTCGCTCTGCCAGTTGTGCAGCAATGAGGTTGGCACGACCACCAGCGCCGGTTTGTCCAGGCGGCCACTCTGCTTTTCAAGCAGCAGATGGGCCAGGGTCTGCAGTGTCTTGCCCAGGCCCATGTCATCGGCCAGCACGCCGCCCAGGCCCTGCTGGCGCAGGTACTGCAGCCAGGACAGGCCTTCAAGCTGGTAGCTGCGCAGCGTCGCGCGCAACCCCTGGGGCGCTGGGACAGCGCTCATCGCCGGGGCGTCCAGCAGGCGCTGCACGCGTGCACGGGTATCGTTGCTGCTGTGCAGCCGTAACTGCGCAGCGTCCTGCAGGGCCTGCAGGCGGCCGCGATCATGCGCCTGCAGGCGCAGCGGTTGCCCACGGTCGCCGAACAGATCCGCAAGCAGCGCGATCACCGGCTTCAGCCGCGCTGCCCGCAGCGCAAGACGTTCATTGTCTGCCGTCGTCAGCAATACGTTCTCGTCATCGCCAATCGCGTCCAGCTGGCCGCGCAGCCAGCGCGGATCGGACTGCAGTACGCCCTGCAGCAGCGGAACCAGCGCAATGCTGCGGCCATCGACGTCGATGGTCAGGGCCAGGTCGAGCTCGTTGCTGTCGGCGGACACCGACCGGACATCCAGGTCGATGTCCTCCACCCGGGTGATGCGGTGGCGGAAGGCGTCGTCAGTCTCGATCTTCCAGCCCAGTGCTTCCAGCCGCAGCACATCCTCCAGCAGGAAGCGGGTCCAGTCGAAACTGCGCAGCTCGAACAACGGGCCGCCGCCGTCCAGCACGATGCGCGGTTGCCGCTCGCGGTGCAGGTGGACGTTGTGCAGTTCAGCCTCGCGCCGTGCCTCCCCGGCCAGGTCACGCGGCAGCAGGTAGAGCTGGCCCTCGGCGTCATGCACGAACAGCGAGGGGTCGTCGAGAAAACGCACGTGTTCGTCGTACTCGAACGCGACGGTGGCGACGTCGAGCCATTGCGAGGGGTCACGTTCGGTGAGCCAGGCAGGTCGGTATTCCATGCTGTGCAGATGCAGGATCGGTGTCATCGCCTGGATCTGCAGGGTAGGCAGTATCGGATCGGCGGCCGCACGCAGCGAACCCGGTTCACCCTCCAGTGAGTTCTGCAGTGCGGCCAGCAACACCGCGGCGACATGCTCGCAGTGCGTGCCAGCCGGGCAGGTGCAGCGACTCTGCAGGGGGCTGTGCGGGGTGCGGGCGCTGGCATCCAGGTCGATCGCCACCTGCCAGCCCTCGACCTGGGCGGTCAGCAGCGGTGACCGGTAGCGCAGCTCGCGCACTGCCGACACCTGGTGGTTGCCCTTTTCCAGCGTCCCGGCATCCAGCCAGCGGGACAGTTCCCCTCCGGTGAATACTTCGGCCAT

Protein sequences of DBSCAN-SWA_2

>NZ_CP040429|622625:631603|625133_626030_+|WP_154879289.1|DBSCAN-SWA
MTVLVFGGNGQVGQELLRALAPLGKVVATTRSGVLPDGSACETADFGQPDSLPALLDRLQPSIVVNAAAYTAVDRAEQEVDAAFAANAQAPGVIARWCAAHGVPFVHYSTDYVFDGQGTAPYREDEPTAPLGVYGTSKRDGEDAVRAAGGRHLIFRTAWVYASHGANFLRTMLRVGAERDQLRVVADQIGTPTPAALIADVTVQALQHPGALSGTWHLTASGQTSWHGFAEAIFAEALATGVLAKVPSVEAIPSSEYPTPAKRPAWSVLDNRKLQQDFGIALPTWQDGLKRVMAELAR
>NZ_CP040429|622625:631603|626121_627525_-|WP_134831974.1|DBSCAN-SWA
MNTVQPVILSGGSGTRLWPLSREAYPKQFLPLAGELTMLQATWRRVAPIASRGPLVIANEEHRFVAAEQLQQVGAEPAAIILEPVGRNTAPAIAVAALEATRDGNDALLLVLPSDHVITDEAAFRAAVQAAAGAAEAGKLVTFGIVPTGPETGYGYIKAADGQGVRAVERFVEKPDLDTATGYVASGQYYWNSGMFLFKASRYLQELERLQPAMLSACRDAWQSARRDADFTRLDRDAFTAVPSDSIDYAVMEKTADAVVVPLDAGWNDVGSWTALRDVSQQDGDGNAHQGDVIAIDCRNTYAYGQRLVAMVGLDDVIVVETDDAVLVGKADRMQEVKTVVAKLKADGRSEATWHRKVYRPWGAYDSIDNGERFQVKRITVKPGGTLSLQMHHHRAEHWIVVSGTAEVTRGDEVILLSENQSTYIPLGVTHRLRNPGKLPLELIEVQSGSYLGEDDIVRFEDTYGRS
>NZ_CP040429|622625:631603|622625_623681_+|WP_140228336.1|DBSCAN-SWA
MPTWLVTGGAGFIGGNFVLEAVARGVKVINLDVLTYAGNLKTLSSLDGNPNHVFVQGDIGDSALVSRLLAEHQPDAVLNFAAESHVDRSIDGPGAFIQTNVVGTLGLLEAVRDYWKALPADQGAAFRFLHVSTDEVYGTLGETGKFSETTPYAPNSPYSASKAASDHLVRAFHHTYGLPVLTTNCSNNYGPYHFPEKLIPLVIAKALAGEPLPVYGDGKQVRDWLFVSDHCEAIRTVLTKGQVGETYNVGGNSEKQNIEVVQAICALLDQRRPRADGQPRSSQITYVADRPGHDRRYAIDASKLKNDLGWEPAYTFEQGIGFTVDWYLDNQEWVNGVLDGSYRLQRIGTAA
>NZ_CP040429|622625:631603|623695_624583_+|WP_025878478.1|DBSCAN-SWA
MTQRKGIILAGGSGTRLYPITKGVSKQLLPVYDKPMIYYPLSVLMLAGIREVLIINTPHEQALFQQLLGDGSQWGMDIQYAVQPSPDGLAQAYLIGRDFVAGKPSCLVLGDNIFHGHGLREVLRNADQRDHGATVFGYWVNDPERYGVAEFDKSGKVVDLVEKPENPRSNYAVTGLYFYDGNASHHAAELKPSPRGELEITDLNQRYLREGNLHLEALGRGYAWLDTGTHQSLLEASNFIETIQTRQGLQVCCPEEIAFGQGWISAEQLEALAAPLIKNGYGQYLHKLALRGVVP
>NZ_CP040429|622625:631603|624579_625137_+|WP_025878479.1|DBSCAN-SWA
MKVIETKLPGCVVIEPAVFGDARGYFFETWNAERFAALGLPDRFVQSNVSTSAQGVLRGLHYQWPRPQGKLVSVLEGEVYDVAVDIRRGSPTFGQWEAVVLSAENKKQFWIPEGFAHGFAVLSERAVFSYLCTEVYLKDFDAGVRWNDADIGVDWPVSAPTLSAKDENAPFLKDIAEDRLPVYVP
>NZ_CP040429|622625:631603|628981_631603_-|WP_154879291.1|DBSCAN-SWA
MAEVFTGGELSRWLDAGTLEKGNHQVSAVRELRYRSPLLTAQVEGWQVAIDLDASARTPHSPLQSRCTCPAGTHCEHVAAVLLAALQNSLEGEPGSLRAAADPILPTLQIQAMTPILHLHSMEYRPAWLTERDPSQWLDVATVAFEYDEHVRFLDDPSLFVHDAEGQLYLLPRDLAGEARREAELHNVHLHRERQPRIVLDGGGPLFELRSFDWTRFLLEDVLRLEALGWKIETDDAFRHRITRVEDIDLDVRSVSADSNELDLALTIDVDGRSIALVPLLQGVLQSDPRWLRGQLDAIGDDENVLLTTADNERLALRAARLKPVIALLADLFGDRGQPLRLQAHDRGRLQALQDAAQLRLHSSNDTRARVQRLLDAPAMSAVPAPQGLRATLRSYQLEGLSWLQYLRQQGLGGVLADDMGLGKTLQTLAHLLLEKQSGRLDKPALVVVPTSLLHNWQSEAARFTPDLRVLTLHGPARDTQFDAIAAHDLILTTYPLLWRDEPALQAHSYHLLILDEAQQVKNPRSRAAATLRTLQARHRLCLTGTPLENHLGELWTQFDFLLPGLLGSEKQFNQHWRHPIERGSDQRHAQLLAQRLRPFILRRRKDQVASELPPKTVITRTVAMEGAQRDLYEAVRVAMEKQVRDAINGSGLARNHIVVLDALLKLRQVCCDPRLLPGETPARAAGSAKLDLLREMLPAMVEEGRRILLFSQFTGMLALIGQALRELSLPYVQLTGDTQDRVTPVQRFMQGEVPVFLISLKAGGVGLNLTAADTVIHFDPWWNPAAENQATDRAHRIGQDQPVFVYKLITAGSVEERIAELQQRKADLADAILEGNGGTGPRFDAADLEALLSPLPGAPAKRAAGRRRATHT
>NZ_CP040429|622625:631603|627539_628886_-|WP_154879290.1|DBSCAN-SWA
MPLPAFKAYDIRGRVPEELNEDLARRIGVALANQLSPGPVVVGHDVRLTSPALQDALAAGLRGAGREVIDIGLCGTEEVYFQTDHRGAAGGVMVTASHNPMDYNGMKLVKENARPISSDTGLFAISDAVAADSATPQPPTAGQRSEHDKSAYIQHLLSYVDSTKLKPLKLVVNAGNGGAGVIVDLLSPHLPFEFIRICHEPDGSFPNGIPNPLLQENRAATAEAVREHGADFGIAWDGDFDRCFFFDHNGRFIEGYYLVGLLAKAALDRNPGGKIVHDPRLVWNTVEMVEQAGGVPVLCKSGHAFIKEKMRAEDAVYGGEMSAHHYFREFAYADSGMIPWLLIAQLISESGRSLADWVEDRMAAYPCSGEINFKVSDAKASVARVMEYFAAQSPALDHTDGISADFGDWRFNLRSSNTEPLLRLNVESRGDAALMQARTDEIATLLKA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140228336.1|622625_623681_+	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	8.3e-80	46.5
WP_025878478.1|623695_624583_+	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	8.2e-97	58.5
WP_025878479.1|624579_625137_+	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	5.4e-46	51.1
WP_154879289.1|625133_626030_+	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	5.7e-29	37.8
WP_134831974.1|626121_627525_-	mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase	A0A1V0SH58	Hokovirus	8.0e-46	28.5
WP_154879290.1|627539_628886_-	phosphomannomutase	A0A127AWJ1	Bacillus_phage	3.0e-34	27.4
WP_154879291.1|628981_631603_-	helicase	A8C6A2	Antheraea_pernyi_nuclear_polyhedrosis_virus	1.4e-48	30.4

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP040429|1645080:1705758|DBSCAN-SWA
GATGATCCGTCACGACGAGGACGCTCAGACGTTCAACCTCGATGCCGAGATGGCGGTGCTAGCCGGCCTGCTGCTGGACAACGACGAGCTGGCCAACGTGCAGGACTGGCTGGCGCCCACTGACTTCTACAGCCCCGATCACGCCCGGATCTACGAATGCGTGCTGGAGCTGTGCGGCGAAAACAAGCGAGCCGATGCGATCACCGCGGGTGAGTGGCTGCTGGACAAGGGCGGGGAAGATGGCCGGCACCTTCAGGCATTGGCATACGAGATCTCCGGCAGTGCCTATACCCGTTCCAACGTGGTGCCCTACGCGGAGGTGGTGGTTGAGCATTCACGGATGCGAAGCTTCATCGCCACCTGCGAGCGCGCGCTGCAGGCGGCGAAGAGCCGTCGCGGTTACTCCGCCGAGCAGCTGGCCTCACATCTGTCGACGCAGATGGCTGACATTGCTCCCGTGCGGGCGGTAGGGCCGCGGCCGTACCGTGAAGTCGTCAAGAAGTTCGCAGCCCAGCTGCGCGACCGGCATTTGAACGGCACACCAATCGGCTTGCCGACGCCATGGGCTGACATCAACAAGGCCATCGGAGGATTGCGGGACGGTCAGGTGATCGTGATTGCTGCCCGGTCCAACATGGGCAAGTCCCTGATGGGTTTCCAGCTGGCCAGGTTCACCGGCCTCCGCGGGGATCATGTGGTCGAGTTCTCTATGGAGATGGTTGACACGGACGTGGTGGCGCGAGACGTGGCCGCCATCGGCGAAATCCCCTTGCAGTGGCTGGTCGGCAACGGCGACGAGGTGTCAGCGGATGATTCCGACCTGTACTGGGGTAAGGCTGTACCGACGATGCAAAGCCTTATGGAGGCGACGGTCCTGGTCGATGACGACCCGCAGCTGAGCGCGCCCCAGATCGTTGCCCGCGCCAAACGCGCGCATCGCCGCAAGCCTCTCCGGCTGGTGGTGGTGGACCACCTCCATGAGATGGCATTGCCGGGCAAGCAGGACGAAGCGCTCGAGCGAGGACAAGCCCTGCGCGACCTCAAGGGGCTGGCGAAGTTCTTGAACTGCCCGGTGGTGGTGCTGGCCCAGCTCAACCGAGCGGGTGCCAAAGGCGACCGTCCGAAGGTGACCGACATTCGCGGTTCCGGTGGCATCGAGGAAGTGGCCGACGTGATCCTGTTCGTTCACCGACCGGACGCGTACAAGCCGGAAGACAGGCCGGGCCTGGTCGAAGTGATCGTTGGCAAGGGGCGCAACATCCAGACCGGGACTGTCGTGGCCCTGAGAAACGAGTTCCAGTATCAGCGCGCAGTTGACTGGGACGGTCCGGCCTACGAATTCGCTGCCGAGCCAGAGCAAACGAAAAAGCGCAAAGCGCAACTCGCTCCCAGACTGGGGATCCGCGGACGCAACTCACAGGGGGCAGACAATGAGTAATTTCATCCCGACTGGGTCCCAAGCGCTCCGCCACCTCGCCGACACCCTTGACCAGCAGGCGGACCGCCTCGACCGCCTGTTGTGGCGGGATCGGGGACAGCGGTCTACGACCGCACAGGCGTACCGCACCTCGGCATCGCTGGCGCGGCAGCAGGCGGTGAAGTTGGAGCAGATGGAGAGGATGGCCGCTGCGCGCGCTGGGGGCGGGAAATGAGCCTGTCGCTGAAGGAGCAGCTGAAACACTGGGGCCATTACCAGGAACATCGGTTCTGCGCACCGCTCGCCCCGGAGGAGGCGCCGAGCAGGGGCGAACACCCGCTGGCCAGGGCTCAACAGTTTGCCCAGGGCACGAAGCGTGAGCGCCCGCCATTGCTCCGCGACGGACACGACCGGCGCATGCTGCTGGGGGCCGGCGCCGGCCGGGTGAATCGCAACGGGGCAGTGCTGCCCGTCGCACCTTGGGCGGTTGATCCGATCCCATGCACTGAGACCCGCACGTTGGTCTCCCGATCAGCCACCGCCGCCGTGATGGTTGGTTCGCCAGAAGAGTATCGATGGATCGACCGCGCGCTGTCCGACCTCTACCGGCAGAACATGGTGCGCGCGCTGGTGGTGCTGGAGGAGTTCACCGGGCGGGGTAGCCAGGCGCAGCGGGCCGCAGCCGTCGCCAAGAAGCTCGGGGCAGAGTTCACGAAGTGGCAGTACCGAAAGGAGCTGGACAAGGGCATGGCGTTCATGGAGGCGGCACGGAGATGAGGCTGGCAAGCACTGTCAATTCTCACGTAATCCAGGCGGCGGTTGACGCGGTATTCCTGCGGGTCGTCTGTTCGGCGAATGGGCGGGTCCGCGTTGGGATCAGTCGGGAGCCGCTTGAGGGGCTGCGTAAGCTAGCAGGGCAGGAAGCGATAGCAGCGCAGTGGGCTTGGATCGGGAGCGCGGCGAAAGGGAAGGCCGTCGAAAGGTCCCTGCGCAAACGCTGGGCCAGTCGATACCGGGTTGGCGAGGGCTTCGGCTTTGACTACGGTACTGAGGGGAGACTGTTCCGCGATGAGCTGGACGCCACCTTCGGGGAAGTCGTCGGCGTCCTTCCCCAGTGGCGCAAGGTGGGGCCGGAAGAAATGGCGGAAATCATCGGCGGTATGCGGAAGGAACGACGCCGGCCCGCACTCCCAGTCAAAAGGAATTGAACGTTGCCAACGCTGGTGGTATTGTCCCGCTAGATTTGGGAAATCTGCACCTACGGCTCGCCACTCGGCGGGCCGTTTGCGTGACCGGTTGCTGGCCTGGTCATCGATGCAAGCCATGGCCGACTGAATTTTATGCAATCCTTGTCCGTTCACGGAAGATCACAGGGGTAGCCAATGAAGTCGAGTAGCAGTCGCGTAATGCGTTTCCTTGAGATTAAGATCTCGCACGGAACCGGTGCAAAGACACGGGAAGCGTGGGATTTGCCCGCAATGCTGAGGACGGCCGCGGGTAACGGCTTTTATCAGCGAGCTGTCAGGGATGGCGCAAAGAAGGTTGTGCGCATCAAGCACTGTGAGTTCTTTGAGGAGAATGGCCGGCCCTACGCGGCTGTTCTCTTTGTCATGGCTGACGCTGGATATATCGATGCCAGCTACGAGAACATGCAGACGGGGGCGGCGCGTACGTTTGCCAAGGACGATGGGGAGGGATACCGCACCGAAGCGCATCTCGTCATCGACCTTTCCTACACTCTCCAGGGTACTACCCAAGTGTATCCCTGCGCGCTCGAGGAATCGCCGGGACTTGGTCCGTCAGTCGTTCTCAGTCGACTTAACCATCCATTGCACAAGGCTGGCGAGCGGGAACTTAAGGAAGGCAATGACACGCATAACTGGTTCCCTGTTGTTTCGCTCGACGGCCTTCTGAGCAGGAGCTTGATCGAGGAGATTGAGAAGGGCGAGCTGATGTCTTTCGACCTCGTGAAGGAAGAGTTGCAAGACCAAGGCTTGGACGAGCCAGAGGAGTTGGTTCGTCGTAGGCAGATCCTATGCCTCGACGTCCGGCAAGATCCCGAAGAGGGGCGAGTCTCCGCCGTCATTGCCCGGGCGCGCCAGATCGCGTTCGGCGAGAACTATGAGCAAGTGCGAATTCACTATAAGGAAGAGGGGACTGGTAAGCATAAGCAAGCTGTGCTTGACGTTCCCGAGGATGCGGTAGATCCGGGCGAAGAGCTCGAGAAGCTTGTATCCAGGTCCTGCAAGATTGAGCTGCCCGAAGCGATGAACTGGGATCACACTGAGGTTGTGTTGACTTTCGCAAAGCAGATGGCAACTAAACTCGCTGAGGAAAAAGGCGACTAGACATGTGGAAAGCGCTACGTCAGTTGATCACACCGCTTGCCTATCTGCGCATTAGCGCCGAAGGCTGGGGCAAAGTCATGATCGATTGGCTTCTGCCCGGCTTGCTGGCTGCGGGCGTAACCACCATTTGGTGGAACTGGCCCTCGCTCGTACCGCTGGGCGGAGGTAGTGGCCTTCTTGTTGGTGTTGGTGCTGTGATGCAGATCTTGGTTGGCTTCTATGTGGCCGCGTTAGCAGCAATTGCCACTTTCCCCACTCTGTCGCTTGAGAATGACGTTCACCGCATGACGTTGGACGGGGGGAAGATAAAAAGACGAAAGCTCCTCGGCTATCTTTTTGGGTACTTGGCCGTGTTGAGCATGGCGATGCTTGTCGCGATGCTCTTCCGCAATCTCCCCCAGGAAGCAGTGAAGTTGGCCAGCCCTGAGGTGGCTCGCTGGCTAAAGGCGCTTGGATACTTCGTTTACCAGTTTGTCCTCTGGCAGATGATCTCCATCACGCTATTTGGCATTCATTACCTCGCGGATCGGATACATCGATCATAGAGGTGCACTAAACCCAAGTTTCGAGAAAGCCCCGGTCTCCCGGGGCTTCTTTATTTCCGGAGACGCCATGACGCAGATCACTCCCCAACAGGCTGGCGGCGTGAACGTCGTGGCCTTCCTCGACATGCTGGCTTGGTCCGAAGGTACGGACAACGGCAAGCAGCCGACCAAAGACCGTGGCTACGACGTGATCGTTGGCGGGCAGTTGTTCAAGAGCTACGCGGACCATCCGCGCGTGCTGGTGGACCTTCCGAAGCTCAAGATCCAGTCCACTGCGGCAGGACGATACCAGCTGCTGCGCCGCTACTACGACGCCTACAAGAAGACGCTCGGTCTGAAGGATTTCTCGCCGCTGAGCCAGGACCTGATCGCGCTGCAGCAGATCCGGGAGCGTCGCGCGCTGCCGTTGATCCAAGCGGGCAAGGTTGAGGAAGCCATCAAGGCCGTCCGCAAAACCTGGGCGAGCCTGCCTGGCGCTGGCTACGGCCAGCACGAACACAAGCTTGCCGACCTGTTGGCCGTGTACCGCAAGGCCGGCGGGACGGTGGCGCCGTGACTGAGCCCGTGAGCACTCTCAAAACCATTGTCGGGACGTTCACCGCGGCCGTTGTGGCACCGGCGACGGCTGATGCATTGCGGGAGGCCGAACGGGTGATCCTCGGCGTACCGCAGTCCGTGCTGCTGGTTGCCATGGCGGGAGCGCTGATCGGCGTCCTGCTGCTGCCTGAGAAGGACGCGGAGCGGGTAGCCGCTGACGCCAGCCGCCGGCGCGGGCACCGCCTCCTGCAGACCGCCGCGCGCTGGGCCGCCCTAGCTGTGGCAGTCGTGGCCTACGCCATCGTGGCCGCATGGGTCATCGCCGTTGCCGCGTCCATCTGGCCGGCGCTGGCGGGCGCCCCCCAGCTGCCCCTGGCCGGCCTGTCCGGCGTCCTGATCCGCCGGCTGTTGCCCGGCTACGTGCGCATGGTGGAGCGAGCCACCGGCGCCATCGGAGGCGATAAGCCATGAGCGTACTGATTCGATTCCTTCGTGCCGTGTGGAGCCTAGTCATTGGCGCCGCCGCCGACGCATTGCAGTGGCTGAGCAAGCCCGGCAGCAAGATCAAGGTGGTGTGCGCGGTGCTGGCCTTCGGTTGCGCGGTGTCCGGGCTGACTGCCTACGAGAAAGAGCAGAAGATCCGCGACCTGAGTGCCCAGGTGGTTAAGGTCCGCGCCGACTGGGAGGCCGATGCGGCCCGACTGCAGGCCGACGTGGACACCCGCGATCAACGCCTGGCCGAGGTAGCCACCGCACTGAGGGCGGAGGCCGAGAAGCTGGAAGCCCTCAAGGCAGAAAGCGCGGTGGCACTACAGGCACTCGCCGGCAAGATCGAGGCGTCCGAGAAGGAGGCATCAACCTGGCGCGGCCGCTACGAGCAGCGGCCCGACACCTGCAAGGCAGCGCTGGAGCTGCTTGATTCCGCCTGCCCAGCATTGAAGGGGTACTGACATGCGCGTCATCGTGGTTGTCACCGCTGCGCTACTGGCTGCATGCCAAGCCGCACCTACCAAGCCGAATCCGCCTGCGCCTGCCTTGATCAAGGTTCCGGTGGCCACCTATGTCCCCATCGATGCCGCCCTGACCAAGCGCTGCAGCTGGGTCCGAGACGGGAAGCCTTCGGCGGTGTTCGACGTGAGCAATGGTCGGAAGCGCTGCCTGATGCAGTACGAGGCCCAGTTCGAGGCCATTGGCCAGGTGCAGGGCAAGCCTGTGCCCGAGCACGAATGATGGCGCAACAGACGGAGCGCCAGAATCGCGTGCTGGCGCTGGGACGGCTCAAGACCGGCGAGATGAACAGGACCGAGGCCGCGTATGCCGAACGGCTGCGCGCGTTGCAGGCCGCCGGCGAGATCCAGTGGCACCGGTTCGAGGGCCTGAAGCTACGTCTGGCGGATAACACGTTCTACACCCCGGACTTTGCGGTCATGGCAGCCGACGGCGTCATGGAGTGCCACGAGGTGAAGGGCCATTGGCAGGACGATGCAAGGGCCAAGATCAAGATCGCCGCGTCCATGTATCCGTTCCGCTTCATCGCGGTGAAGGTCAAGGCCAAGCGGGACGGCGGCGGCTGGGCAGTGGAGGAGTTCTGATGGCTGGAGCAGTGACGGCTAACGTCCGCATGCGCTGGTGGCTGCGGTGCTACTTGGCCGCGGTGGTGTGGTTTGCCAGGAAGACGGGCATGGAACCGGACTGGGATCGGGTCGAGCGGTGGATACGCCGCGGCTTGGTGGTTCGAGGCGCAGGGGCAGACCAGTGAGTGTGGCTCGCGGCCGCCGGACCCGACAGACCGGCGGTAGTGCCTTCGCCCAACTGTACGGCACCGCGCGCTGGCAGCGCACACGCAAGGCGCAGCTGGATCGCGAGCCATTGTGCTGTCGGTGCAAGGCACGCGGCCATGTGACTGTGGCGACGGTATGCAACCACACGAACGGACACCCGCCTGGAGAGACCGAGGAGATGTTCTGGTCTGGACCCTTCGACAGCCAGTGCGCCGACTGCCACAACGTCGATCAGGCCCGTTTGGAACGTGGTGCGGTGCAGGTCCGAGGGTGCGATGAGGACGGATGGCCGGTCAACGGCTGACCTGTTCCACGGCGAAGCGTTCCACGCCGAGGGTAGGGGGGGGGAATTTATGCCATTTCCCGACGCCTAGACCGACCGTTCCCGGAAACACGCATATCCACAATTCGTCGGACGACCCCTTTTCGAGCGTCTGAGACCACAAATCCCCGCATTTTTCAGAGGAATCCATGGCAAGGCCTCGACTGCCCGTCGCAAAAGCTGCGACAAGCGGCGCCGCCATCAAGAACCCTGGCCGGCACGCCGGCAGGAAGCGCCCGACCGGCGTTCGCGCCTTGGGCGAGCCCTACAAAACGATGACGGCCGGCGAGAAGCGGGCGTGGAAGGAGTTCGCCGCAGAGATGCCCTGGCTCAACGCAAGCCACCGCGTGCTGCTGCGCCTGGCTTGCCTCTGGACAGCTCGCATGGAAGACCCGAAAGCCGAATTCGGCGTGTCAGCAACCCAGGCGCTCAGCTCGATCTTGTCGAAGCTGGGTGCCACTCCTGTGGATGAATCGAAGGTTTCGCATGGCGGTGACGACGAAGACGCGGGCGAAGAATTCTTCGCCGGCGCAGGCTCCGGCCGATCGCACTAAGGCATATGCGCTGGACGTGGTAGCTGGCCGCATTGTTGCCGGGCCACATGTACGCAATGCCTGCCGTCGCCACCTCCAGGATCTAATCCAAGGCCCCGAACGGGGCCTTTTCTTTGACCACGAAGCCGCCGACTACGCGTTCCGGTACTTCGAGAACGTGTTGATGCTGTCGGAGGGCCAGTTCGAGGGTCGGAAGTTCGAGCTGCACCCGTCGCAGGCGTTCATCATCGGCTCGCTGTTCGGCTGGAAAGGGCCGGATGGTCTTCGCCGCTTCCGCCGTGCGTACATCGAACAGGGCAAGGGCAACGGGAAAAGCCCGCTTGCCGGTGGGCTGGGCCTGTTGGGGATGACGGCAGCGGGTGAGGCCGGCGCGCAAATCTACGCGGCGGCGGCCAAGAAGGACCAGGCGGGCATTCTGTTCGCCGACGCCGTGAAGATGGTCAAGAAGTCGCCGCTGCTGGCCAAGCGAGTGGAGTTCGCTGGCGGCGAGGGCCGGGAATTCAGCATGGCGCACCACGCCAGCGCGAGTTTTTTTCGGCCCGTATCCCGCGACACCGGGCGTACCGGTTCCGGTCCCCGGCCATACTTCGTGCTGGTCGATGAGGTGCATGAGCTTCCCGACCGGCGAATCATCGAAATGTTGGAGCGCGGGTTCAAGTTCCGCCGCGAGCCGCTGCTTTTCATGATCACCAACTCCGGCAGCGACCGAACCTCGGTCTGCTGGGAAGAGCACGAACATGCGGTGAAGGTTGCAGCCGGCCACACCGAAGCGGTCAACGATCCGACCTTCATTGGCGATGTGATTGATGACCGCACCTTCAGCTACGTGTGCAGCTTGGACGACGGCGACGACCCGCTCGAGGACCCCAGCTGCTGGGCGAAGGCCAATCCCCTGTTGGGGGTAACGATCACCGAGCAGTACCTGGCGGATGTGGTGGCGCAAGCCAAGGCCATTCCCGGGTCGCTGAACGGCATTCTTCGGCTGCACTTCTGCGTGTGGACCGATGCGGAGACCGCTTGGATGACACGCCCGACGCTTGAACCGGCCCTGGCCGACTTCGATCCGCACGTGCATGCCGGCCGCAAGGTTTACCTCGGCCTCGATCTGTCCCAGGTGCGGGATATCACCGCGATGGCAGCGGTGGTCGAGACCGGCACGGTGCCGGTGGAGGTCGAGGTTGAGGGCGAGAAGCTCATCATCGAGAAGCCGACATTCGACGCCTGGATCGAGGCGTGGACACCCGGCGACACGCTGGACGCGCGGCAGCTGCAGGACAAGCTTCCGTACCGCGCGTGGGTCAACGGTGGGTTCCTGCACGCACCGCAGGGTCAGGCGATCAACTTCCGGCACGTGGCCCAAGTCATGGCCGAGTACGACAACCGGTACGTCGTGCAGCTGGTCGCATACGACCGGTATGCGTTTCGGCGCTTCGAAGAAGAGGTCAACGACATTGGCTTGTCGGTGACCTTCGCCGAGCACCCGCAGGGCGGCTGCAAGAAGGGCAAGCCATTGGACGCAGCGGTCGAGGCGGCCGAGCAGTCGGGCCAGCCAGCTCCGGAGGGTATGTGGATGCCCGGATCACTACGGTTGCTGGAGGAAGCGCTGCTGGAAGGGCGCCTGCGCCTGCGTCGGAACCCAGTGTTGGTGTCCGCAATCATGTCCGCCGTCATCGAATCGGACCGCTGGGGTAACAGCTGGCTGTCGAAGGCGAGGTCGGCAAACAAGATCGACGCCGCGGTGGCCCTTTGCATGGCCATCGGCGCGGCACACGCCATGCCGCAGGACTCCGGCGGCATTGATGACTACCTGGAAAACGGCTTCTTTGGATTGATCGGATGACAACTTTTCGCTGGTACAACCCGATGAGCTGGCGGTTCTTCGGCTATGACGACCCCGCGACGGGGAACTACGTCGAGGTCGACCTCTCGGTCGGTGGAAAGGGCACGAAGGCCGGTGTTCGCGTAACCCAGAAGAGCGCCCTTACGGTCAGCATCGTCTGGTCGTGTGTGAAGGTGCTTTCTGAGTCCGCTGCCGGACTGCCCTGGAAGCTCTACGAGGACACCGGCGGCCTGCGAGCGCTCGTGAAGGGTAACAGCGCTCAACGGCGGCGCTTGCTCAGGCTGATGGCCAAGCCCAACCCGTACATCAAGTGGTTGGACCTGATCAAAGCCGTGGTGGTGAACATGGCGCTGCGTGGCAACGCCTTCGCCATCATCCAACGCGACGACAGCGGCGCATGGATCGGCCTGATTCCGGTCGGAGTGGACAGCGTCCGCATCGACACCGACGACGGCCTGATCTACTGGGCAACAATCAACGGCAAGGAGACACCTGTCTCGCCGGAGAACATGCTGCACTTCAAGCTGTTCAGCCCGGACGGCATCGTCGGCCTTTCACCGGTGGAGTACCAGGCCGAAACGATCGGCTTGGCGCGCGCGGCGCAGGACTGGTCAGCCCGGTTCATGCGAAAGGGCGGCTTCACCGGTGGCTACATCATCTATCCCGGGTTCCTGACCAAGGAGCAGCAGGCGCAGATCAAGGCGAAGCTGCCGGACATTCGTCAGGGTGATGTGGACGACCTGGGCAAAATGGCCATCCTTCAGGGTGGGCCAACCATCACGCCCGCCGGCTTGACGCAGAAAGACAGTCAGTTCATCGAGTCGCAGCAGTTCCAAGAGGAAGCGCTTGCAGGCATCTGGGGCGTTCCGCTCTACCTGACCAATCGCGCGCGCTCGACCTCGGTCCTTGGGTCGAACCTTGAACAGCAGACCAGCGGCTTTGTGACCTTCGGCCTGAAGCCCTACCTGGACGCGATCGAAAGCGAGATCAACGACAAGCTCTTCGCTGAGACGGAGATCTTCGTTGAGGCCGTCGTGGAGGGCTTGCTGCGCGCGGATAGCGGCGCCCGCTCCACCTACTACAAGACCGCCCTTGGCGGCTCCGGTGGCTCGGGCTGGATGACCATCAACGAGGTGCGGGTGAAGGAGAACCTCCCCGCGCTCGACGGTGATCAATACAACCAGGTCACCCGGTGGACCAGCAACCAACCCGATTCCAGCAACGACGACCCAACGGGGGATCCCGCCAATGCTTAGCAAGTACTCCTGCCCGTTCGAGGTCAAGGCGGCGGACGACGCCGGCAACTTCGAAGGCTACGCCTCGGTGTTCAACAACGTTGACCTCGGTGAGGACCTGATCCTGCCGGGCGCCTTCGTCAAGGTGAAGACGACCAGGACTGGCCGGCTACGTCTGGCGCTGTACCACAACCTGACCCGTTTGATAGGCGATGCCGAGTTCAAGCAGGACGACAACGGCCTGCACCTGAAAGGGAAGGTCAACCTCAACGTCAGCTACGCCAAGGACGCCTACGAGCTGATGAAGGCCGGCACGTTGGACGAAATGTCGGTCGGCTTCAACACGCTAGAGGACGCGATTGAAAACCGCGAGGGACGGCGGGTGCGCGTCATCAAGAAGGCCGAACTGTGGGAGGCCTCGGTCGTCCCCTTCGGCATGAACCCGGAAGCACAGGTGATGAGCGTCAAGTCCGACGTTCGCGCCTTCGAATCAGCCCTGCGCGAACGCATGGGGCTGTCCCAGAAAGAGGCGGCGGCCGTCGCCTCGCTCGGCTTTCCCGCGATCCACCGAGACGGTGGCATTGGGGACACGGAGACCGTGAAACAGCTGCAGAAACTCGGCAACTCCATCCAATCCATCTTTGAAGGAACGAACTAATGCCGGACAACATCATTGAGATCCGCGAAGGCCTGGAAAAGCAGCTGAAGGACGGCTTCGCCGGCCTGCAGAAGAAGTACGACAGCGCCTCGGCCGAGATCGAAAAAGGAAACCAGGTCACCACCGACCTGAAGAAGCAGATCCAGACCGCCACCGATGAGATCCAGAAGGTGGTGGACAAGGTCCTGAAGCTGGAAGAAAAGGGCATCGGCCTGGGCAATCAGCCCGGCACGAAGAAGGGCTTCATCGACTTCATCAAGGGCAACGACGAGTACAAGGCGCTGCAGGGCCGTGAGAAGGCAGCGGCTGAGATCGAGGTCAAGAAGGACGAACTGGCGTCCATGCAGGAAACCAAGGCTGTCACCAGCGCCGGCATCGTGGTCCCCAACTTCGACCCGACCATCCAGCCGGGCATCCGCCAGGAACTGCGCATCCGCGACCTGATCCCGTCGATCTCCGTCACCGGCCAGAGCTATACCTACTTCCGCGAGAAGCTGCACACCCGCGGGGCCGGTGCGGTCGGCGAGGGCACCGCCAAGCCGCAGAGCAACGTCACCTTCGAGCAGAAGACCGATCTGGTGAAGAAGCTGGCGGTCTGGATCCCGGTCACCGATGAAGCTCTGGACGACGTGCCGCAGATGTACGGCTACCTGCAGCAGCTGCTGCGCTACGACCTGAAGCTGGAAGAAGAAGCCCAGATCCTGAAGGGCGACGGCCTGGGCAACAACCTGCCGGGCCTGATGACTGACGCCACGCTGTTCGATGACGACCTGTCCAAGGCCGGCGACACCTCGATCGACACGGTTCGCCGCGCGATCTATCAGGTGCGCAAGCAGTCGAAGCTGTCGGCCGATGCCACGGTGATGACCGAGCTGGACTGGATGAACATCGAGCTGGAGAAGGACAGCCAGAACCGCTACCTGTTCGCCAACCTGCAGGGCTTCGTGACCCCGATCCTGTGGGGCCGCCCGGTGGTGGCTTCGGACAGCATGGACGAGGGCGACGGCACCACCACCGGTGGCGAGTTCCTGGTCGCCAACTTCCAGCGCGGCGCCACGATCTACGACCGCATGAGCTTCCTGTTCAAGGTCGGCCTGATCAACGACGACTTCGTTAAGAACCAGCGCGTGCTGCTGGTGGAAGAGCGCCTGGGCCTGGCAAAGCGCCGCGTCGAAGCGTTCGTGAAGGGCCGCTTCAAGCCGCAGGTCTAATCGCCTCCAACCACGAGAGAGGCCGGCCATGCGCCGGTCTCTCTCCCGATACCGAGTGACGAAGATGAAAATCAAAGCACTGTGGGGCTTCCGTGGCGATGCCCCGAAGCTCAAAGCCTCGTCTGCCGATGTGAAGGCGGGCGATGTATTCCCGGACGTGGAGCCCGAATACGGGCACGCGCTCGTCGGCAAGGGCTTGGTGGTGCAGTTGCATGAAGGCGCAGCGCCCACGGAGACGAAGCCGGCCCAGCCGAGTGAATTCAAGTCCGGCGATGGCGACACATCCGCGGCGGCAGCTCCGGACGCCCAGGCGAATGCGGTGACCGACGCCGGTGGCGCGCAGACGGCCAGTGTCGATGCCACCGCCGCTACGCAGCCGACAGCTGCTGTCGACGCGGGCACCGATGGTGTCGCACATGCAGGCGGCGCAGATGATAAGCAGCAGCTGATCCAGCAGCTGGAGGCGGCAAGCGCCACCTTTGACCGTCGCTGGGGCGTGCAGCGTCTGGCAGAGGTGCTGGCGGACGCCCAGAAGAACAAGGACCCCGTGTAATGGCCGTCACCCTCGATCTTGAGCTTGTTCGAAAGCAGTGCAACGTCGTCGCCGACGTAGACGATGCATTGCTCCAGCAGTACGTAGCGGCCGCTTTGGCGCACATCGAACAGCACTGCGACCGAAAGTTGGTCGAGGGTGATCCTTCCGGCCCGGATCAGTTGAAGTTGGAGGCCGACGTCGTGCAGGCAGCGCTTTTGCTGGTAGGGCACTGGGTTGCCAACCGCGAGGCGGTCGTCATCGGTGAGGTATCGACCGCTGTCCAGTTCGGCGTTGAGCGGCTCCTCTGGTACAGGAAGGCATTCTGATGCGCGCCGGATTGCTCAATCGAAAGGCCCGTGTCGAGCGGCCAGTGTCTGGCACCGATAGCTGGGGCCAACCCTTACAAGGTTGGGAGCTTGTAGACGAGATCATGGTGGGCGTTGCCGGCGAGACCGGGCTCGGCGCAATCCGGGCTGGGCTACTGGGAGGCGTGCCTGCATCGATTTCCCGCTACAGCTTCATGGCCAGGTATCAGACCGTGAAAGCGCTTGGCATCGACGCAACGATGCGGATCCTTTACGAAGGGCTTGTGTTCGAGGTGAAAGGAATTGCCCGCGATCTGAAGCACAAGGATCGGGCCTTCATCATTACCGAGGAGGGGGGCAACAGCGGATGAGTATCAAGGCCAACATTGACTTCTCCGACGCCGTGAAGGGGCTGGACTCGCTGTTGGAAGCCCGCATCAGCTTGGCGCGTTCCATGGGCGTCGCTGGCGGACAGGTAATCCGCGATGAGGTAAAGCTGCGGGCACCGGTTGGAACAGAGGAGGGCGGAAGCCTGCGACCAGGCAGCCTTCGCGATGCGATCTACTTGGCGTACCGGGACGGTCGTTCCACCGACAGTCTGCAGGTCTACTCGGTGTCATGGAACGCCAAGAAGGCGCCCCACGGGCATCTAGTCGAGTTCGGGCACTGGCAGACGCACGCGGTCTACAAGGACAAGGACGGCTCCTGGACGCTGGGTGCGCCCCTGGCGCAGCCAAAGTGGGTGCCTGCCAAGCCGTTCGTGCGGCCCGGCTACGAGGCGTCTCTGGCACGTGCGCAAGCGGCGATGTTGGAAAGGGGCAGGGAGCGGCTTCCTGAGCTGCTGCGTAAGGAGCGAGGAGGTGCCGGATGAGCTACGAACCGTCCCTACATGCCCTGATCGCACCCTTGGTGCAGGGGCGCTTCTACCCCGACGCGCCGCCGGACCAGCAGGTCTTCCCATTCGCGCTCTACCAGCAGGTCGGCGGCCAGGCTCTCTGGTTCCTTGAAGGATCGATGCCGGACCACAAGCATGCGCGGGTGCAGATCACGGTATGGGCTAAATCCAGGCCCGAGGCCAACACGCTGATCCGCCGTATGGAGGACGCGATCTGTTCCGGCGTTCCGCATTCCGAGCCCTATGGTGCCGCAGTCGCCATGTACGAGTCGCCCATCAAGGCATACGGCGCCCGTCTCGACTTCGGGCTCTGGTTCCCTGACCCGTAAGCCACCCACCAACCCCGCATCAGCCCGGCCAAGTGCCGGGCTTTCAATTTCAACCAGAGGAACACAACACATGGCACTCAAGCTCCCGAAGGGCACACAGTTCGGCTTCGCTCAGGTGGTGTCCACCGCGATCGCAACCACAGGTATCTCCAAGGCCGCGCCAGCGCTCGTCAGCGTCGCCGACGGCGCCGTGGACACCGATGACGTGGTGGTGCTGGAGATCCCCGGCTGGCCGGCCTTGAACAACCGCACGACCCGCGCTGGCGCCGAGTCCACCGGCGCAATCGAACTGCTGGGCACGGACACGACCGATACTGTCCTCTACCCGGGCACCAGTGGCGCCGGTACGCTGCGCAAGGCCGGTACATTCATCGATCTTGACCAGCAGGGCGACCCGACCACCGCCGGCGGCGAGCAGCAGTACTGGAGTGGGACGCTGCTGGAAGACCCGACCGGCCGTCAGATCCAGATCCCCACGTTCAAGAACGCCAAGACCATCACCATTCCGCTGTACTACGACCCCTCAAAGCCCTGGTATCCGGCGCTGAAGACGGTCGACGCCAAGGGCGAGCCGGTGGTGATGCGTGCCAAGCTGGCAGGCGGCGATGTTCTGTACTGGTATGGCTACCTGAGCTACGACGGTGATCCGACCATGACCGCCAACACTCCGATGGGCACTACCGCGACTTTCACGGCTCTGGCCGATTCGATTCTCGTGGAGGCTGCCTGATGTTCAAGGTAAAAGCGCCGGAGACCATCAAGGCATCGCTGACCATCGTCGGCCATGGCCGTGAGCAGAAGCTCAACCTGACCTATCGCCACATGACCCAGGAAGCATACTCCGCAGTCCTGGGGCGCTTGGCCGGTCAGGAAATCACTTCGACCCAGGCGATTCTCGACATGGTGGTCGAGTGGGATGCGGATGTTGATCTGGACACCGCCGGCGTCGATGAGGCGTTGCAGCAGCAGATCGGGTTGGACGCGGTGATCATCACCGGCTACGCCCAGGCCATCCAGGTGGCACGCAAGGGAAACTGATCGAGGCGGTGGGGGCGCTGTACTGGCGCGCCCCCACCGAGGCCGAGCTTGCGCAGGTTGGCCTCAAAGCGAAGCACTACCAGCCGCCGGAGGTGCAGCTGTGGCCCGAGTGCTCGCTGCCTATCGAAATCTTCTCCCGGGTCTCCACCCAGTGGCGCGCAAGCGCCGGAGGACCGTTTGGGCTGGACTACAACGTAGTGTTTCAGGAACTGGACCGCGAGGGTCTGGAGGGTGATCGCCGGGCTGAAGTGATGGCGGCACTACGCATCATCGAAGGTGAAGCTATCCTGCAGATCAACAGGGGCTGACCGACGCCCCGCCCCGGGATACCATTCGATCATTCAGAAATGGAGGCCCGAGGATGGCACTGATCAAATGCTTGGAGTGCGGCAGGGAGGTAAGCGACCTTGCGTCCATTTGTCCTGGGTGCGGTGCCCCCATCGCAGCATTGGGCTCAACCCCTTCATCCGTTCATCCGCAGAAGCGACGGTCATTCAAGGTCGAATGGTTGGTTCTTGCCGGTGTACTCGTTCTTGGAGTTGTCGTCCTATTGATTACAGGCTTGCGGCCGTGGCCGGGTGAGACTGTGCAACAGGCGACAACACGCAGGGCGGAGATGAGGAGCGCGCGAGATGCCATCTCATATTGCGACAAGCGATATGCCGAAATGAACCAAGATCGCCAGTATGGTCCGTCGGAGCTGAGGCTCCACGCGGACACCTGCAAGCTGCTCAGGAAGCAGTACCGAGAGCATTGGGGCCGGGATCCGTAGCGATCCGATCCGTCGTCGAAAACATGCCCGCCCATGTGGCGGGTTTTTTATGTCCGAGGAAATGTATGTATGACTGACCAGTCCCTTGGCGCCGCGCGCATTGACTTGGTAGTCGATACGCAGCAATTCGATAGTGCAATCAGTGCAGCCAAGCGCGGCGTGGCCGACATGTCGGGGAGCGCCCAGCAGCAGTATCATCAGCTGTCGCGCGCGGAACGTTCTCGGGTCGATTCTCTGGTGCGCCAGGCCGACACCTTGGGCATGACTCGTTCGCAGCAGTTGGCCTACAACGCCGCGCTGCGCACCAGTGGGCCGGTGCTGGACGAGATCGTGCAGAAGCTTGCACGGGCCGAGGCTGCAGCTAAGCGCTCAGGCAAGGAGCTGAACGCTTACGGCGTCAGCGCCGCCCAGCAGGCCAACGCCATGCGCGGAGTGCCGGCGCAGATCACCGATATTGCGGTGAGCCTTCAGGGAGGCCAGAACCCGCTGACAGTATTTCTGCAGCAGGGTGGGCAGCTCAAGGACATGTTTGGTGGGATTCGTCCTGCGGCCGCAGCGCTGGCTTCCCAGTTGCTGGCGTTGATCAATCCCCTGACCATCGCCGCAGCGGTGACCGGTGGCCTGGCGTTCGCCTGGTATCAGGCCAGTGAGGAGCAAGGGCGCTTCCAGCGTGCGTTGGTGCTTACCGGTGGCCACGCGGGGTTCACTGCCGAGCAACTTGGGGAAATGTCGCGCGCGCTGGATAGTTTGGAAGGCATCACGCGCGGGAAGGCGGCTGCGGCTCTGGCAGAGGTGGCACAGTCGGGGCGCTTTGCGGGCGAACAGTTCGAACTGGTTACCCGCGCAGCTTTGCAGATGAACATTGCCACCGGGGCATCCATCGAGGAGACCATCGGCAAGTTTGCAGAGTTCCGGAAAGATCCCGTGAAAGCCCTGCTTGATCTCAACAGGGCCGAGAATTTCCTGTACCAATCTCAACTAGACCGCATCGTGGCATTGAGGGACGAGGGGCGCGAGCAGGATGCTGCAGCTGAGGCAATGCGCTTATACGCCGATGTAGTGGAGGACCGTACGGGAAAGGTCCTCAACTCTCTCGGGCTGGTAGCAACGGCCTGGAAGGAGATCAAGGGCGCAAGCGGTGAAGCATGGGATGCCATCACCGAAGGCGCGGCTAACGCTGATCGCGGTCTCAAGCAATTTGCGGATCGCGTAGCCAACATGCCACGGGTCGCGCAAGACCTGACCACGTACGGCCTGGCGATGGTCAACCTGCCGCTGGCGGCGGTAGTGCGGCTTGGCGGTGATAGGTTCGGTGGCGTAAAGGGTACGGTTGACTCGACCGCCCCGCTTGCGGGGACCATCGATTCCGATCAGGCCGAGAAAGCGCTCAAAGAACGAAGGAAGGCCCAAGAAGAGTGGGAGCGCTTATCTGGCCAGAACCTCAGCAAGCGGCAGAAGCAGCTTGCTGAGGAGGCGAACATCGTTGCCCTTGGCAAGAAGCTCGGCAAGGATCAGGCAGATATCGACCGCGAGGTGGCTGCCTCTCGCAAGCAGTTCGAGGAAGCCGAATCCCGGCGCAGCGGCGGGTCCAAGTCGAACCCGGCCACGGCAATTGTTGCGCAGATCCAGCAGCAGGTTGCGCTGAATAAGGAGCAGGTTCGCAGCGAGGAGAAATTGAGCGTAAGCCAGCGCCTTCGAGTGCAGGTGATGGAAGAGCTGGATCGCATGGGGGGCAAGATCCCCGAAGCCGATCGCAAGCGCATCAGGACGATGCTGGAGGAGCTGCGGGCTACAGGTGCATTGGTGGAAGCCAAGGACAAGCAGAAGAAGACGTTGGAGGCGCTCACGCGACAACAGGCGATCTTCGACCAGCAAACCGAGTCGCGCCAGCGCGCCAATGAGCTGGACCTGATGGGCTACGGCCGCGGGCAGGACACCGTCGCCCAGCTGCGCAGGCAGATGGACGTACAGCGGGAATACGAGGACGAGCTGAAGCGCTTGGGTGATCGCCAAGTGGCCACCGATCAGGACCAGTGGGATCAGCTTGCGGCCAATGCAGCCAAGCATAGGGATGAGCAGCTGCAGCTTGAGACGGATTACCAGGCTCGCCGGCTTGCCGCGATGGGGGACTGGCGAAATGGCACGCGCGCAGCCTTCGAGGACTACGCCACCGAGGCCAACAATGCGGCAGGCCAGGCGCACTCGGCGCTGACGAACGCGTTCCAAGGCGCGGAGGACGCACTGGTTCAGTTTGCAATGACCGGGAAGCTGTCTTTCCGCGACCTGGCCAACTCGATCATCGCCGACCTGGCGCGGATCGCGGCAAAGCAGGCAATTGTCGGAATCGCCGGAATGATCGCTGGTGCATGGGGCGGAGCCGCGTCAGCAGGTGCGTCCTCGGGGACGTTGCAGGGATTCGGCAATAACACCAGCTGGCTCACTGCGAACGCCAATGGCGGCGTCTACAACACGCCGAGCCTGTCGACGTATTCCGGCGGTGTCTACAGCTCCCCCCAGCTGTTCGCCTTTGCGAAGGGAGCGGGTGTGTTTGGCGAGGCAGGGCCGGAGGCAATCATGCCCCTGCAACGCGGGCCTGATGGGCGCTTGGGTGTCGCGGCTCATGGCGGTGGTTCGGGAGCGTCCCAGGTGAACGTGAGCGTGGTGGTCAACAGCGACGGATCGACCGACGTCTCCGCTGACACACCTGTGTGGCAGCGATTCGGCAAGGAAATTGGCCAGCTCATCGACATGAAGATCAACGATGCGCAGATCCGATCAATGAAGGACGGCGGAGCAATGAGGGTGATGGGGGGCGGCCGATGACCGACACATTCCACTGGCAAGCCACCAGTCAGAGCAGCGGCACGGCGACTGCATCGGTCAGGCGCGCAAAGTTCGGTGACGGCTACTCGCAGCAGGTGGCGGAGGGCATCAACTCCGTTTCCAGGAAGTACCAGCTGAGCTTTGTCGCGTCGAAGGCAGTGATTGCCGAGATCGTCGCCTTCCTCGATACCCACGTGGGCGCTTCCTTCCTGTGGGCCAGCCCGTGGGGAACGGGCCTGTACTACTGCGATACCTACACCGATTCCCACCTTGGTGGCCTGACCTACAGCGTCACGGCCACCTTCGAACAGACGTTCCAGCCGTAAGGAAAGGCCATGGCACGACAGATCATTGATACTGACACCCAAAACCCTGGTTGGGTCGGCGACATTGCCAAGATTGCCTTCACCAAGGCCAATGAGAACTTCGGAGAGTTGTACGCCGTCCTGGGGAGTGGCGGTGTCATCGACGCTCGCATTCCGGCAAAGAACCTGCTGATTAACGGCAACATGCGCGTTCTGCAGCGGGGCAGCTCCGGCACACTCAACAACACGGAAGTGTTTGGGCCGGACAGGTGGAAGATCGGATGCCTTGGTGGAGTGACCTGCAACTGGGGTGTTGGTCAGGCCCCTGCAGGTACGCTCCGCAATAGTCGATTCTTCCTCGGCTACAACGTTGTAGCGGGCGCTTCAGCTTGGATTGGCCAGAAGGTGGAAGGTGTTCTCACGATCCATGGCGACAAGGCCACCTTCTCCTTCCTGATGCGTTCCACACCTGCGGGGCGCAAAGTGGGCATCCGGATCATCCAGGACTTCGGCACCGGTGGCTCACCGTCGGGGCAGGTAGTCACCGAGGTCGGGGTGGTGACTCTCGGGGGCGCTTTCGAACCGCATAGCGTGACGTTCGACGTACCCAGCGCTGCAGGCAAGACATTCGGTTCAAGCGGGACCGACCATCTGTATCTGTTGATCGACTTCAGCGGGAGCGGTCACGGCGGCCAGATCTCCGGCCAGACGGGGTTGTTCGAGTTCAGCGAAGCGCAGCTGGAGCGAGGCTCTAAAGCCACTGCGTTTGAACACGTTGCCATGGCCGATGAAGTGGAGCGGTGCCAGAGGTATTTCCAGAAGAGCTATGACCTGAATATCGTGCCTGGCACAGCCAATGCCACAGCCGGACAGGACACGTTCTTCTTCTACGGCGACCCGAACAGTGGTCGAGCGGTGGGCATGACATCGCGCTTCGCCACTCGTATGCGCGGCATACCCGCCGTTACGATCTATAGCCCCGCGACTGGTGCCGCGGGACAAGTAAGAAGTGAGGCGCCGGCTGGCGACTATGTGGGTGGGGTAAACACTCCTGGGCAATCCGGGTTCTTTCTTACTACCGTCGCCATCACCACCAACAATACCAATGTTCGTTGGCAGTGGGCAGCGGACGCGGAGCTCTGACCATGTACCGATACACGCACGATCCGGACCTTCTTGTTTGCCTGGAAACAGGAGCGACGATCCCGCGAGGAAACTACCTGTGGCCGGGTGACTGGCTTGCCTCCGGCGGTGTGCCTGAACCCATCGCGCCGCCGTACGTGCTCTATTCCCCAGAGCACTTCCGGGCAATCCGAGACGCAGCCTTTGCATGGATGGAGGCTGAGGTCAAAGGCCGCGGCTACGACAGCATTGCCAACTGCACCTCCTACTTCAACAGCGGCGTGGAACGCTATCGCCTCGAAGCGAGAGCGATGGTGGCATGGCGCGATGACGTGAATCAGGCGCTGGAACGCCTGGTGGTGAGCCCGCCCGAAGGTATCGAGACGTGGGATCAGGTCCGGACGCTGCTGCCGCAGCCCATCGCATACGAATGGCCGGCGACAGTCGAGCTGCCGCTGGATGCTGGTGAGTCCGCCCCACCGGTGGTGATGTCGTGATCACCGCCGATGCCCAGCAACTCGAGCCAGGTGCCCGTGTCACGGTCTATGAGCTGGACTGCACCAGCTTCGGTGCCGATCAACTCTTCTTCCACGCGCACCTGCAGTCCGGGTCGATTTGGTGGCAGGGACAGGAGTATGGCCCTTGGCCGATCAGCGCTACGGGCTTCGAGCGGACCAGCGAGCAGCAGCCAAATCCGCGGTTGAAGGTCAGCAACATCAACGGCACGATCGCCGCCCTGTGCCGCATGTTCCAGGATCTGGCCGGTGCGAAGCTAATTCGTCGGCAGACGCTGGTGAAGTACCTGGACGCGGCCAACTTCCCCGAGGGCAACCCGCTAGCCGACCCGGGCGAGCACTTCCCGGATGAGATCTGGTACATCGAGCGCAAGGTCGGCGAGGACGACGAGACGGTCGAGTTCGAGCTGACGACGGTGGCCGACTTCAACGGCAGGCTGCTGCCCGCGCGGCAGTGCACGAGGATCTGCAGTGCCCTGCTGCACGGCGGATATCGCGGCCCGTACTGCGGCTATACCGGCTCGGCCTACTTCGATATCAACGACCAGCCGGTGAGCGATCCGGCCAGGGACGTGTGCGCTGGCCTAGTCCGAAGCTGCCAACTGCGGTTCGGCCAGGACAAGCCGATCCCCCACGGTGGGTTCCCAGCCGCCGGCCTGCTGCGAACCTGAAGACCCGCCGAACCACACCAACAAGACGTTCGCGCTGCACCAGCAGCACCACAAGGCCCGCCCAGCGCGGGCTTTCTTTATGGGCGAGATTCATGCAACAGACCACCCTGCAGGCCATTCAGGCGCATGCCGTGGCCGAGTATCCCCGCGAATGCTGCGGCCTGATCGTGGCCGGCGCCGATGGCGAGGCCTACATTCCATGCCGAAACGTGGCCACCACGCCCAGCGAGCACTTCCGGCTGCCGGCGGAGGACTTTGCCGACGCCGAGGACGTGGGAGAGGTGCTGGCTGTCGTGCACAGCCACCCGAACGCCTCTGCGGCTGCCTCCGACGCCGACCGCGTCATGTGCGAGGCCAGCAGGCTGCCGTGGCACATCGTGAGCGTAGGGCAGTGCGTCGGGGCCGATCCCGAATGTGGCGACTTGCAGACCATCGATCCCTGCGGGTACGAGGCGCCTCTGGTTGGCCGGCAGTTCGCCCACGGCGTGCTGGACTGCTACAGCCTGGTGCGGGACTTCTACGCCCGCGAGCTGGGCATCCGGCTCAGCCAGTACGAGCGGGAGGACGACTGGTGGGAAAAGGGCCAGGACCTCTATGGCCTGGACCGCTTGCGTGCCGAGGGCTTCGAGCTGATTGAAGGCGAGCCACAACGCGGCGACATGGTCCTGATGCAGATCCGGTCACCCGTGCCGAACCATGCCGGCGTCTACCTTGGCGACGGAAAGATGCTGCACCACATGCACGGCCGCCTTTCCGAGACTGTCGTGTACGGGGGCATGTGGGCCGAGCGGACCCGCCACATCGTCCGCCACAAGGAGACCGGCCATGACTGAGCGCCTGCGCACTGTTCGGCTGTACGGCCGCCTCGGCGCCCGCTTCGGGCGCAAGTTCCAGCTGGCGGTGAACAGCCCGGCTGAGGCCATTTTCGCACTCGGCGTACTGCTGCCTGGCTTTCGCCAGTTCCTGACCGGGTGCAGGGACCAAGGCATCGAGTTCGCCGTGTTCATCGGCCGCGAGAACCTGAGCAAGGCGCAGCTGCACGATCCGCCGGGTGCCGACGATATCCGCATCGCTCCGGTGCTGGTCGGCTCCAAGCGCGGTGGTGCGCTGCAGACCATCGTCGGTGTGGCACTGATCGTCGTGGCCACCATCTACGGCGGTCCGCAGGCTGGTGCTGGCGTTGCCAAGTTCTGGGGCGCTATCGGCGCGGCCGGCTGGAGCCTAGCCATCGGCGGCGTGGTGCAGATGCTGTCGCCCCAGCCGCGTGGGCTAGGGACGAAGGAGAGCGCCGAGAACACGCCGAGCTACAGCATGAATGGGCCTGTGAACGTGCAGGCACAAGGCAACCCGGTGCCCGTCGCTTACGGCGGCCACGACACGAAGGGAATGGTCGTCGGATCGGTGGTGATCAGCGGCGGCATTTACGCGGAGGATCAGCAATGAGTGCATTTCTGCTCCCAGGCACACATGCGGCAGTGGCGCTGGTGAGTTCTGGAATTCTCGGCGCCGGTGGAAAGAGCAGCACCAACGCCCGCACGCCGGTTGAGACCCCGGATAGCCTGCACTCGATTTCCTACGCCAAGGTCCTGGACCTGATCAGCGAGGGGGAGATCCGGGGGCTGGTGGCCGGTAACCAGTCCATCTACCTCAACGAGGTGCCGATCCAGAACAGCGACGGCACCTTCAACTTCAACGGCGTGCGGGTCGAGACCCGCTCGGGCACGCAGGACCAGGAGTACATCCCGGGCTTCCCGTCTGTTGAGAACGAGATAGGGGTCGGCGTTGAGCTGCGCGACACGCCGGTGGTACGCGCGGCGTCCGGGCAGGATCTGTCGGCGGTGCGGATCCGGTTCGGTGTACCCGCGCTGCAGCGGCAGAACACAGAGAATGGCGACACCGAGGGCTATGCGGTCGAGTACGCCATTGACCTGTCCACGGACGGTGGCGCCTTCAGTACCGTGCTGAGCAACGCCTTTCGAGGCAAGACGACTACCGAATACCAGCGTAGCCACCGCATCGATCTGCCGCCGGGCAATCAGTGGCAGGCGCGGATCCGCCGCCTAACGCCGAACGCGAACAGCGCCACCGTCGCCGACACCGTGAACGTGATCTCGATGACCGAGATCATCGACGTGAAGCTGCGCTACCCCAACTGCGCGATCGTTGCGGTTCAGACCGACGGCAGTCAGTTTCAGGGCAAGCCGACCACGGCCTACCGTATCTGGGGCCGGATCATCCGGGTGCCCAGCAACTACGACCCGATCGCGCGCAGCTACACAGGCGTGTGGGATGGGACGTTCAAGTCTGCCTGGACGAACAACCCGGCTTGGGTCTACTTCGACATGGTCACCAACGACCGTTTCGGCCTGGGTGATCGCGTCCCGCTGGACTGGGTCAACAAGTGGCGCCTGTACGAGATCGCGCAGTACTGCGATCAGCTGGTCAGCGACGGCATGGGCGGCATGGAGCCGCGCTTCACCTGCAGCCTGTACCTGCAGACCCGGGAGTCTGCCCATAAAGTGCTGCAGGACATGGCCAGTATGTTCCGCGGCATCAGCTTCTACGCGGCAGGCCAGATCATGGCCTCGGCGGACATGCCGAAGGACCCGATCTACACCTACAGCCAGGCGAACGTTGTCGATGGGAAGTTCACCTACATCGGTAGCGGCGGCAAGGCGCGTCATACGGTGGCACTGGTGTCGTGGTCCGATCCCGACGACTTCGGCAGGCAGAAGGTCGAGCCGGTCCAGCTTCAGGAAGGCATTGCGCGCTACGGCGTCAACCAGATCGAGGTCACGGCCTTCGGCTGCCACTCCAAGTCGCAGGCTCAGCGCGTGGGGCTGCACATCCTCTACAGCGAGAACCTGGAAACGGAGACCGTCAACTTCGCCGTGGGCCTGGATGCTCTGAACTGCATGCCTGGGGATGTGATCCAGGTGGCGAATGCAAAGCGTGCCGGCCGGCGCAATTCTGGTCGAATCAGCGCGGCATCGGCGAGCAGCCTGACCTTGGATGTGGTGCCGACCTCGATGCAGGTCGGTGACCTCCTGCGCGCGACGCTGCCGAGCGGGAAGACCGAAGCCCGCACCATCAACGGGATCAACCCGGGAACGTGCGTGGTAACCGTCTCTGCGCCCTGGAGCGCGGTGCCGGTGGCGCAGTCGATCTGGGCGACCGAATCGACCGACTTGGTGATGGAGCAGTTCCGAGTCATCAGCGTCACGGAGGAGGATGGGCTTACCTACCGCATCACGGGCCTGACTCACCGCCCGGACAAGTTTGCTGCCATCGATGACGGCACCCGGCTGGAGCCGCCGCCGATCAGCATCGTCCCGCCCAGCGTGCAGCCGCCGCCGGCCAACGTGCGCATGTCCTCGCATGTGGTGATCGATCAGGGCATCGCCACGCCGGTGCTGACCATCGAATGGGATGCGGCTGACAAGGCGATCGCCTACGACGTGGAATGGCGACGGGACGACCTCAACTGGGTGCGTGCCGGGCGGGTGGCAACGGCCAGCACCGAGGTGCGCGGCATCTACGCAGGCAAGTACTTGGCCCGGGTGCGGGCGGTGAACGCGCTCAATGCCGTTTCGCAGCCAACCCTCAGCGCGCTGACGGACATTCAGGGCAAGACGGAGCCGCCGCCGGCGCTGACCTCCCTCACGGCCACCTCGGTGGTGTTCGGTATCCAGCTGGCCTGGGCGTTCCCGCCTGGAGCAACCGATACCGAGCGCACCGAGATCTGGCGCAGTGCAGGCCCGAACCTGGAGAACGCGACGAAGATGGGCGACTTCGCCTATCCGCAGAACCGGTTCCAGCTCGATGGTCTGGCAGCGGGCGCCAAGTTCTACTTCTGGGGCCGGTTGGTGGACCGCAGCGGCAACATTGGGCCGTGGTATCCGGCAGGTGCGGGCGTGGTGGGCGAGTCGAGCACGGACGCGACGCTCTATGACACGTACTTCTCCGGGCTGATCAACAAGAGCGCGCTGGGCCAGGAGCTGCTGTCGGAGATCGAGAGTATCAGCGGGATCGTGCCGCTGATCTGGGCTGCTGATGCCACCTACGAGCCGGGTCAGACCGTGATTCACAACGGGAAGATCTGGAGCTGGAAGGGGGCCGGGCCGGGCAACGAGGAGCCGCCCAGCGCCAACTGGCTTAACGTGGGTGATGCCGTCGCACAGGCCGGTGCGGTTGTCGGCAGGGTCAACTCGCTGGAGCTGGCGGTCAACGACCCAGATACGGGCCTGCAGGCCGTCGGGCGCAAGACGGATGGCCTGTTCGCTCAGCTCGATGCGCAGGGCGCCGGCGATGCCGACTGGGGCGCCGGCAACGAGAACGTGTTTGCCGGCACGACGACCCTCCAGACGGTCATGGTTGAGGCGGACCGCGCGCTGGCCAAGCGCGTGGATACCGTCGAGGCATCGGTGGGCGATATCGACCTCGGTGGCGTCCAGGCATCGGTGCAGCAGACCAGCCAGGCCATCGTCGATCTCAACGGCAGGATCAGCGCCACCTACACGGTCAAGGCGCAGATCACCAGCGCTGGTCAGATCTACATGGCCGGCATGGGCTTGGGTGTCGAGCAGCAGCCCGATGGCAGCTACCAGAGCCAGATCCTGATGCAGGCCGACCGGTTTGGCGTCATCAACGTGGTCAATGGGAACGTGACCGCGCCGTTCGTGATCCAGGGCGGGCAGACGTTCATCAACCAGGCGCTGATCGGCACTGCGTGGATCACCAGCGCCAAGATCGCCGATGCCGCGATCACCAACGCGAAGATCAGCGGCACCATCCAGTCCGACGATTACGTGTCAGGACAAACTGGATGGCGGATCAACAAGGCGGCGGGCGGGGGCTTCGAGTTCAACGGCACTGTCGCTGGCGGGTATAGGCTGAACATCACCAACCAGGGCATCTACATCCGATACCCGAACGGCAATCTCGCCGTCGAACTTGGAGTGCTGCAGTAATGGCTGACGTAGGTCTGCGGGTTCGGAGCGAGAGCGGGTACGTGGAGACCACCGTCACCACGCGGCTGACCAAGATCATCGGGTCCTACACGTTCCCGCTTTACAACCCGGTCAACTCGAACAACAAGTGGATCGCGCCGCCCGCGGCAAACGGTGGGCTCATCGTCAATGACTTTTCAGGCGGTGAGCCCTTCTACTACTTCACCTGCGAGGGCCAACGATCTGTGTACGGAATGCTGGTCCCTTCGGTGACCATCTCGGGGAACAGCATCAACTGGAGCTGGGACCCTGACGTGGTGAACTTCCACGTCAGGATGGAGATGTTTCCGAGCAAGCCCACGACGGACACCGTCGGCGGCATCACCCTTCATTACGGGATCTACAGCTGATGGCCGTCGGATTACGCGTGCGAAACCAGGGAACCGGGCAGATCCAGATCGGTCTCGGCTATCGAAACCTGCAGCTGGCCAAGTCCGGGACCTTGAACACTGGGTCCTTCTCCGGTGGCGGGACCGGCGGCTCGCCGCCGTTTGCCTCGTGGTCGCCGAGCGGGGTCCTGGCTTCAACGAACGGGACAACGAACCTCCATGTCTGCCGCTACATCAACGACAGCGTGGCAACTACGACGGGATTCACTCTGGTTCAGACCGGTGTGACGTGCTTCGTCTACGCTTCCAGCCAAGCGCCGAACAAGACGCTGGAGTACTACACGTTCAATGCCACTGAGCGTGCGGCCAGTGGACCGGTTGGTCTGCGCATGCGTGGTGAAGACGGCACGGTCTTCTACGATTCAAGGCGCAAGGGCCTGCGGGTACTCCAAGTGGTGGCGTTGCCAACAGTCCCTGGGCCTCCCGTAGAGATCGGCCAGTTCTTCCCAGGGACGAAGATCGGCATTGCCATTCCGTCCCCGCGCTTCTACTACTTCGCGCAATCGCAGGATCGGTGCACCATGAATGCCGATTACTTCCACATGACCAGTGATAATCGAATCTTCCTATCCCGGCTGCAGGTGACTCAACAGACGCTGATCACCAACACCTTCCCGGTTGGCGGCGTAACGATGGGACCTCAGAACGCGTCGATCTTCATCGTGGACCTGACCGAGGTGCCGCTGGGGTTCGGCTGAGAGCAGGCCCATCACACCGTCGCAACGCGTGCTGCGGCCAGATTGTGGCCATGTGCTATTCCGCCCAAATCGAAGCCGCCTACCAGAAGCTGGTCCGCATGACCGGTGCCACCGTGTCGCTGCAGGAATTTGCCGCGCTCTACGCCCATGACCCGGGCAAGAAGCGCCCGAAGACCCCGAAGGCGATGGATGACGCGTTCCGAGCCGGCACCAGCCCGGCAGAGCGGGCCGTGTGGGCGGAGATCCAGCAGTGGAACCAGGCAGAGGCCACGATTCTGGAGCAGGAGCTTTTCGCCAACCGGAAGCGCTTGGCGGATGCGGAGCGATCGCTGCAGGCCAAGGAGACGAAGAAGGCCCGGGAGGACGTGCGGATCGCCGGCAAAAAGATCGAGCGCGCCATGGGCAAGCTGGCCGACCTCAAGCGCACCGAAGGCAAGGACCGGGACAGCCGGATCTTCCCCGGGGTCTACGCACCGGTGCTTGTCTCCGACGGCGGCAAGCTGACGATCAAGCCGATGCGCTATCAGTGCCGACTGGCCGGCAAGCCGGCCAACTACGACCAGCGTTTCCCCGGCACCTACAACGCCCGCCGCGACAGCCTGGAGAAGTTCTGGGCGCCGGCCTTCGGCCACACCCACGGCTTGATGGTGGTCGATACCTTCTACGAGAACGTGGAGGGTCCGGACGGCAAGAACCAGGTGGTGCAGTTCACCCCGCGCACGCGCGAGCCGATGCTGGTGGCCTGCCTGTGGTCGCATTGGGTGGACCCGGCCGGCAAGGAGCCGGATCTACTCTCGTTTGCCGCGATCACGGACGACCCGGAACCCGAGGTGGCCGCCGCTGGCCACGACCGAACGATCATCAACATCAAGCCCGAGCACGTCGACGCCTGGCTGAATCCTGATCCTGCCGACCTGGCCGCGCTGTACCGGATCTTTGACGACAAGCGGCACCCGTTCTACGAGCACCGGCTGGCAGCCTAGGGGGCATCCCTATCAAGCCCAATCTGCTCGGTTAAAATTGTCAAAGATTGCTGGAATGCTGCGACAAACAGCGGGCCTTCGTCATTGGCGTGGGTGCTTGCGATCGACGGGAGCAGCCTTGTCCATGTGTCGAGCAGGGCGCTTGGATCTTGATGAGTCAGAAATGAAACGCGAAGAGCGTATTCCATCGCCTTGAGGTAGCCCCGATGCACCTCAAGTCCGGCCTCGCAGGCATGAAGGCGGTCCAGGATTTCGGTGATCTCGGTGCTCATGACGGGCTCGACAGGTGTTGGTGGGAAGGCGATAGTTGGCGGACGCCCAAGCGAGCCCGCTATGAGTATCCTCAACGTTCTTCTCAGCCCTGACCAGCTACTGGTGGCGGTGGACACTCTGGCGGAAGACGCTTTTACCGGTGAAGCATCGACCGGGGCGAAGTTGCTGTTGATCCCACAGCACAACTTGGTTCTTGCCGCTCGCGGCTCTACGCAGTTCTTCCTCAGGATGTACGAGTTGTCCCTACAGGCCAGCTTCCGGGCCGACTTCACCATGGAGCAGCTGATGAGGGAGCTGGGCCTGGTGATCGACAAGCTTTGGCCCGCCTACGAAAGGGCAGCGATCGATGCCGGCCTACCTCGATCCGTGCTTGGCACCGAGCTCGTCCTCGGTGGTTGGTCGTCGAAGAGCGGGCGAATGGTGGCAACCGCCTATGCCAAACACGACAGCGCTGCCTCGGCGATAGTCCAGCCTCTGGACGGCGGGCTCGCATCTCCAGGCGAGCCTCTGGAAGGGCGGCCCGACAGTTTTGAGCTCGTAGACGTGCTGCATGCGGGCCGCCTACAGTCGGCGTGGCTCAATCAGGCTGTCGGCCGCCAAGTGGCAGGCGGTAGGCTTCTGGTTGCCTCGCTAGGTGAACGCCAAGCGGTTGTCCAAGACCTAGGAGCGCTTTAGGTCGTCGGGCACGATGCCCGCAAGTGCCAGCGCACGATCGCGCCGCATCTGTTCTTGCCAGTGGATTCGGGCATCCTCAAACGTCAGCACTTCGCTTGCCTTGCAGACTAGGCAGGTGAGCTTCACGCCACCCTCTGTGTCTTCAAGGCCGCAGCCTTTGGACATTCTCGATTCGTCCCCGCACGCCGTGCATTTGGACTGAAGCGAAGCGATCCCTTCCATCGTTCCGTTGAGTTGGAGAGTGGGCCTGATCCGCAGGATCCGGAAGACTTGTGTATTCGTCATGCGTGTAGATCACAAGGCGTCTGGTGCCTTGATCGTACATATAAATTGTTAAGAATGGTTCTCTTGACAGAGTGTGAAATGTAGAGGTGGGGGCTTAGGCATGGAGCTTGCGAGACAGTCGAGTGGTTCGCACGAGTGGTTCGCAGCATCTGCGACGGGTCTCCGTATCCTTCGCCCATGCTTCCTTCTCACGGCTACCAAGGCTTCCGCTCAGCACCGCCACCCTCTGGCTGGGTCCAGCTGAGGGATACCTGGGTGCTGTGGTGGGGCGGCCGGCAGATCGCCCAGATCTCGCCGGCGAAGGAGCGCGGGGTGCGAGTGCACCTCGATGCCCGGAAGATGTGGCAGACCAAGGATGTATGGGCGGCGAGCGTCGACCAGGGCAAGCGCTACGCCGAGCGGTGGTGCGCGGCCAGGCTCTACCCAGAGATGCGGCTGCGAGCCGCTGTGGCTCGGATGGTGGACGACTCCCTGAGGGAACCCCTACCGCCGCTGCCTGGCCTGCCGCCGACACCCGAACAGTTGCAGCAGGCCCGGCGTCTGGCCGAGGCGGGGGCGAAGGAGCTGGAGCGGGTCAAGGAAGCGCTGGAGCCGCGCCGGCCGCTGGCGGTGACCAAGCCCATGGCGAAGGATCCCATGAAGGCGGGGGTGAGGACGGCAAGGACAGAATAGCGGGGCATCGCCTAAACAGCCTGGTCATCCTTGATCAACCGCTTAGACCGTGGAATCGCCGAGTGCGCGCGCTACCAGGTGTGGTCTCAGTCGGAACTTCTACATAGATTTACTCTGTTCTGTGGCGCCGGCGGTACATGCCCTTCGATTTATGGCTTACCCGTGCCAACCTCGAGATTTGGCAACTCGGTGAAGGCAGCTGTCAGATGTATTACGCTGGCCAAGTAGTCGTTTGCGTTGAATCGGAGGCGTAGATTCACGCCTCGTGTACTCGCCTCGACGCAGCGAACGCTGAGTGAGCAATGGGCCAAGAAGTCAATGTCCTTCAGCTGCCTATTGTTATTGTAGGCTGCATGCATCGATCGGAGTACGGCATTTCGGAAATCTTGCGCTTCCGATTCCTTCTTGGCATTTAGGAAATGATTGATTGCAACCACCGTGGCCAGCATCCTCTTGCTGAGTGCTCGTACGGCGTCCGCTAGGTCTTCCGTACTTGTTTCTACCAGTTTTGCGTACTCTTGCGGTGCCGCGAATCGCAAGCACGAAATGAGGCAGTCGATCGCCGGAAATCGGAATTGTCCCGCGGGGTGGCTTCTTACGAACGCCATCAGCAGGGTGTGCGCTTGGACGGAGTCGCGAAGTTGCATCCCAAAGGATGAAGCAACATATGCGAAGAATATGCTGTATTCAGCTCTGTCGAGATTGGCTGGCGAAAGATCTCTTAGGGCATCATACGCCTCAATTTCGCTTATTTTAAGAAGTCTGCGCCTAAGTTGTTCCGCGTCTTCAGCAGGGTCTGTTCCTGGGAAATTCTGGAAGATCTGATTCGCGTGATGCGCTAAGCTGGGGTGAGGGAGGTTGAACTCGAAATCGAAGAACTTTCGAAGGTATAGTTCGCCATCAACCTCTTGGCCGTAGAGCGTCTTGACCGCTTGCGGTAGGTTTTTGTGATCCGTTGCGATTAGAAAACAAATTCCTTTGACGTTAAAAAAGTGCTTAACTCGCTCCAAGAATTTTATTGCGAAATCAGGGCGACACCGATCAAGCTCATCCACAATGATTACTATGGGCGATGCGTCATTTGACTTGAGGTGCTTCGTCAGGCGCTCTCTGGCTTTCGATAGGTTTTCCCTGAAGCTTTCCTCGGCCGATCTCCTTGATCTGTCCCAGTCAAGGAAGTTTTGCGCTATATCTGGCAATTTATCAGCAACATCGACTGCGATAGATCCTCCTGGGACTAGGCCTGCGAGGATGGAAAGCGCCGGCAGAGCAATTTTGGCGGCAGATTCGGCTAGGCCTCCGATAATGACGTCGGCTGCCTTTGATGTCTTGCTTTGAGTGTCTTTTAGACGATCCGCAAGCGCGCTGGTCATGGCGAGGAGCGGGTCATCCAAATAGTCGGAATGCCAAGCATCGATCCTGATCACTGGGATTTTATGGGAGCCTTCTAGGTGGTATCCGAATCTCTTGAGAAATATGGACTTTCCGGTCCCCCAGCCGCCCTTCAAGGAAATTACGAATGGGGCGTCATTTAGCCCGGATATAAGGCTCGCAAGAATTTTCCCTTGTTCAATTCGAGATAGTGGGTCATTTGACCAAGGGTCTGTAGAGTTGATTTTAGGTTCTAGCGCCTTTCCAAGCGACATGAATTCCTCCTTGTTGTAGGTGATCTTTTCAGCATCTTTGATGCTTTGTTGCCGGCCTCGATACATTCATCTAATTTTTTGGGGGCAGCATAAGCCATGCGCATCGTAACCTTCAGCCATCATCCCAAATGGCGCGCGATCTCCGAAGCAGGCTCGTGGTAGTAGATCATCAAAGACTTGAGGTCCCGATGTCCGATGATTCGAGCCAACTGCAGGATGTCCAACTTTTTCGAAAGCCTCCAGATGGCCTCGGCTCGGCTGTCGTGGAAGTGCACTTCGCGATGACCCGTCGAGTCCCGGACCTTTCGCCAGAGCGCATCACGCACGGCAGATTTAAGCTGGAAGACAGGCCCGAAGCCAAGAGGAAGTGCCTTCAGGATCTCGCAGGCCCGCCGGCTAAGCGGCACATCTCTCGCGTCGCCGTTCTTGGTCTTGGGTAGGTGAACGTACTGCTCGGATAGATGCACGTTTGGCCAAGTCAGTGACAGGATCTCACCTGACCGCATTGCGGTCTCAAGCGCTAGAAGGAACGCCAGGCCCGTCCGCTGGGTGGCCGTCTCCGCCGACAGACCCTTGTCAAGCCCGAATGCTGCGATCAGGTCAGCCTCCTCGGTGGGCGACACGCGCCGTGCCCGGCCCTTGGGCTGCTGGGGCCAGCGCACATCTGACATCGGGTTCTGCTTGATCCACTTCCATTCTCGGCGCGCAGTCTCAAACACGGACCGCATCAAATTCATTTCGCGAGCAACCGTCCCAGGCTTGACCTGCTTAAGCCTTCCATCTCGCCAAGCGATGATGTCTGAACTGTCGATTGCCGCGATACGTCGGTCCAAGAGCGGCAGAGACCTTTCCCAGGCGGCGATGCGGACCGACTCCCACCGTTCGCCAGCTCGCTTAGGCGCCTCTTCCTTCACGTAGCGGTGCATGGCCTCGCGTAGCGATTTGTCGGGGAGCTTCCCGCCACGCAACTCGGCCTCGCGCTCGAGCGCCCACTTCGCAGCTTCCTGCTTTGTGTGTTTGGTGGTGGAGTCGCGAACGCCCGCCACGAACACCTGTACGCGCCACTTGTTCCCTGATCGTTGGATGCTGGCCATGGCCGCATCATATGGGGAATTTTTGGGGAGAGTAGTCGGGCAAGTCCGGGCAAATCGTGGTGATCGGGGAAATTTCGATCACCCTAAGTGACTGATTTCGTGCCGAATCCGGGTGAATCGTGGCGGACGCGTTGGCTCCCCGAAACATGCGATGGTGCCCGGAGCCGGAATCGAACCGGCATGACCTTGCGGTCGGCGGATTTTAAGTCCGATGCGTCTACCAGTTTCGCCATCCGGGCCTGCAGCGCGCGCCGATTGTAACGGAATCGCCGCCGCTGCCGCCGCTGCCGCCGGCTAACGCGGCTTTTACGCAACCGGGCGCGGCGCTGGGTACAGTCCGCCAACGTTCCCGGGAATGGCGATATGCGTGCACGTGGCAGGCGATGGATCGGATGCAGTGCCGTGCTGGGGCTGATGCTGGCGATCGGCCCGGTCGCCGCGCAGCAGGGGCCTGCGCCCACCGGGGCGGTGGTGGACATGGCGACGGTGCAGGTGACCGGCGAACAACCCGGCCCCGGCCTCTGGAAGGTCACCGCTCCACAGGGGAATGTGTTGTGGATCCTGGGCACGGTCTCGCCGTTGCCGAGCGGTGTGCAATGGCGCTCCGACGAAGTCGAGCGGACCATTGCCAGCGTCGACCATGTGCTGGGCGATCCGGGTTTCGCCCTCGATGCGAAGATCGGTGTGTTCAAGGGTCTGACCCTGCTGCCACTGGCATTGAAGACCGCGCGCGATCCGCAGGGGCGCACGCTTGACCAGATCCTGCCGCCGGCAACGCACGCGCGCTGGCTCGGCCTGAAACAGACCTACCTGGGCAATGACCGTGGCGTGGAAAAGGACCGTCCGCTGGTGGCCTCCGGCCGCTTGTACCAGGCTTTCCTCAAGCGCAACGGCCTGCGCGATGGCAAGCAGGTCAAGGAAGCACTCGGGCGCGCGTACAAGGCGCACGATCTGAAGCCGGAAGACGTGCAGGTCAAGCTGAAGGTCGACGACATCCGTGGCACGTTGAAGGAGCTGCAGGCCACCGAAGTCGATGACCGCGCGTGTTTCGAACGCACGCTCGACACGGTGGAATTCCAGGCACCGGTGCTGCGCGAGCGCGCCAACGCCTGGGCGCTGGGGGATGTCGCGGCACTGCGTCGGCTGTCGGGTTCGGCGATGGCCCAGACCTGCCGCGAACTGCTGCAGGATTCGGCCTTCGTGCGCCGGCGCGGCTGGAGCGATATGCCGCAGCAGGTACGCACGCGCTGGCTGCAGGGCGTGGATGCGGCGCTGAGCCGTCATCCAGGCACCTTCGCGACGGTGCCGGTCAGCCTGCTGCTGGGCGAGGGCTATCTGGATGCGCTGGTGCAACGCGGTTATCAGGTCGAGTCGCCACCGGAATAGCCAACGCTTGAAGTCCTCGTGCTTCCTGTCATATTCCTCTGCACTCAGGAGGGGAGTGATGGACATGCCGTTGCATGCGTACGCTTATGTCAGCACGGCCAGGGAGGGACTGGACGTGCCCGAGCTCGATGCATTGCTGGCCGATGCGACCGCGTTCAACCGCATGGCCGGGGTGACCGGGGCGTTGATGTTCGATGGCAGCCGTTTCCTGCAGTACATCGAAGGCCCACGGGATGGGCTGGCTTCGGTGCACGCGCGGATCGGCAACGCGCGTCGCCACGGCAGCATCATCCAGCTTGCCGCAGGCCCGATCCCGAGCCGCTGGTTCCCGCGCTGGACGATGGCCAACCGGCACGTGGATGCGGCGACGCTGGGCAGCATCGTGGCGGCCCCGTGGCATGGTTTCAGCCTGGGGCAGGAGCCCCCGGAGCATGGCTTCTGCCTGTTGTTGCGGGCCTGGACGGGGCGGCACGGCGAACTCGAGCCGGCTGCCGTCAGCCTCGGATCCTGATCCGGGCGTGGTCTGGCGCGGCTGCCGCGGTTAACCTTGTCGGCACGTTTGCCTGCTCCCGGATCCTCGCATGACCCAGTGGACACCATCGCCGCCTGTTGGACGCCGCGCATGAGTGCGCCGATCGGCGCAGCACAGAGCCCGTCCCCGGCCATCATCGGCCTGGGATATGTCGGGCTGCCGTTGGCAGTGGCGTTCGGCCGCCAGCTGCCCACCCTGGGGTACGACATCGATGCTGCGCGCATCGCCGAACTGGCCGGCGGGCAGGACCACACGCTGGAAATGGAGCCGGACGAACTGGTCAGCGCGTCGCTGCTGCGTTACAGCAGCGATCCGGCGCAGCTCGACGCCTGCAACGTCTACATCGTCACCGTGCCCACGCCGATCGACGCCTACGAGCAGCCTGATCTTGAGCCTTTGCGCTCGGCGACGCGACTGATCGCCAGCCATCTGCGCGTCGGTGATCTGGTGATCTACGAATCCACCGTCTACCCGGGTACCACCGAAGAAGTCTGCGTGCCGCTGCTGGAACAGGGCTCGGGCCTGCGCTTCAACGAGGATTTCTACTGCGGCTACAGTCCCGAGCGGGTCAGCCCAGGTGACCGCCAGCGGCGCCTGGCCGACATCCGCAAGATCACCTCCGGTTCAACGCCGGACGTGGCTGCGGTGGTCGATGGCCTGTACCAGCGGATCATCACCGCCGGTACGTTCCCGGTGCCGTCGATGCGGGTCGCCGAAGCGGCCAAGGTGGTGGAGAACATCCAGCGCGACGTCAACATCGCGCTGGTGAACGAGTTGGCCCTGATCTTCGATCGCCTCGGCATCGACACCCAGGATGTGCTCGACGCCGCAGGCAGCAAATGGAACTTCCTGCCGTTCCGGCCGGGGCTGGTGGGAGGCCACTGCATCGGCGTGGACCCGTACTACCTGCTGCACAAGTCCGAAAGCATGGGCTACCACCCCGACCTCATCCACACCGCCCGGCAGGTCAACAACCGGGTGGGCGAGCATGTGGCCAAGCGCGTGCTGGCGATGCTCGCCGAGCGTGGCCGCATGCCAGCGCACTCGCGCATCCTGGTGCTGGGCGTGACCTTCAAGGAGGACTGCCCGGACCTGCGCAACAGCCGCGCGCTGGAACTGGCCCAGCGGCTGGCCGGCAGCGGCGCGCAGTTGGACGTCAGCGATCCGTGGGTGGGGCCAGCTGCCATGGCGGACGAGGGCGTGAACTGGCTGGCCGAGCCGGTGCCCGGCAGCTACGACGCGGTGGTGCTGGCGGTGGCGCATGAGAGCTTCAAGGCGATGGACGATGCCCATATCCGCAGCCTGTTGGCGCCCGGTGGGCTGGTCTATGACGTGAAGTCCGCCTGGCCGCGCAGCGTGGTCGACGATCGCCTGTAGGTGCATGCGCGGTAGACTCGGGGCAGTTGCAACCGAGGAACGCCATGCACCGGTATATCGTCTACCTGCTCGCCATCCTGATGTTTCCGATCTGCCTGTGGCTGGCCACGATCTGGCCGGCCTGGTACTGGGGCGTCGGCATTACAGCTGCGATGGTGGCGCTGGGGACCTGGGACCTGCTGCAGAAGCGCAGCACCCTGCGCCGCAACTATCCGGTGATGGCGCACTTCCGTTATGGCCTGGAATCGATCGGCCCGGAGATCCGCCAGTACTTCGTGCAGAGCGATCTGGAGGATGTGCCGTTCTCGCGGCAGCAGCGTGCGCTGATCTACCAGCGCGCCAAGAACCAGATGGACACGGTGCCCTTCGGCACCCTGCGCAGCACATATGCGGTGGACTACGAATGGATCAACCATTCGCTGGCGCCGACCACCATCGCCAAGCATGATTTCCGCGTGCTGATCGGTCCGAACTGTGCCAAGCCCTATTCGGCGAGCGTGTTCAACATCTCGGCGATGAGTTTCGGTTCGCTGTCGGCCAATGCGATCCGCGCATTGAACGAAGGCGCACGCCTGGGGGGTTTCTACCACGATACCGGCGAAGGCTCGATTTCGCCGTATCACCGGGAGATGGGCGGTGACCTGGTCTGGGAGATCGGCTCGGGCTACTTCGGGTGCCGTGACGAAAAGGGCGGCTTCAGCGAGGAACGCTTCGTTGCCAATGCCAACCACGATCAGGTGAAGATGATCGAGATCAAGCTGTCGCAGGGCGCCAAGCCCGGCCATGGCGGGGTGCTGCCGGCGCCGAAGGTCACCGCCGAGATCTCGGTGACGCGTGGCGTGCCGATGGGCGTGGACTGCGTGTCGCCATCGCGCCATTCGGCCTTCTCCACGCCGGTTGAACTGCTGCAGTTCGTGGCCCGCCTGCGTGAACTGTCCGGTGGCAAGCCGGTTGGTTTCAAGCTGGCCATCGGCCACCCGTGGGAATGGTTCGGCATTGCCAAGGCGATGCACGAGACCGGTCTGCTGCCTGATTTCATCGTCGTCGATGGCGCCGAAGGCGGTACCGGCGCGGCACCGGCCGAATTCGTCGATCACGTGGGGGTGCCGATGCACGAAGCGTTGCTGCTGGTGCACAACACCCTGGTCGGCCTGGACCTGCGCGAGCACATCCGTATCGGCGCTGCCGGCAAGATCACCAGCGCGTTCGATATCGCCCGCACCATTGCGATGGGCGCCGACTGGTGCAATGCCGGGCGCGGTTTCATGTTCGCGCTGGGCTGCATCCAGTCGCTCAGCTGCCATACCGACAAGTGCCCGACCGGCATCGCGACCCAGGATCCGGCACGCTGGAAGCATCTGGATGCACCGGACAAGGCCACGCGCGTGTACAGCTTCCACGAGCACACCCTGCACGCGCTGAAGGAGTTGCTGTGCGCGGCGGGCTTGAACGATCCGGCCGAGCTCGGGCCGGAACACATTCTGCGGCGGGTGTCGCCGGTCGAGATCCGTTCGCTGGCCTCGCTGTATCGCTACCTGGAACCGGGCGAGCTGCTGCACAAGGTGCCCGACCACGCGGTGTTCCATTCGTTCTGGGCGGACGCACGCAGCGATTCGTTCCAGCCGCCACCGAAGATCCAGGCGCTGCGTGCCAGCAAGTCGCGATGACCCGCGTTGCAGGACCGAGCCCATGCTCGACTGCACGAAAACCATCCATGCAAGGAGGCTGCATGCAGTTCAGGACGGGTACCGACGATGATGTGGGCACGCTGTGGGCCCTGCGAACGCGCTGCGTACGTGAGCTGTGCAGCAGCCACTATCCGCCGGAGGTGATTGCACCCTGGTCGGCATCGCCGCCGCCGGTGCAGTATTCGCGGCTGCTGGGGCAGGGCGGCTGCGTCGTAGCCGAGGATGACCGGGGCAATGTGCTGGGGTTCGGTGTGTTCGATACCGAGGGCAACGAGATCGATGCGCTGTTCGTCGATCCGGATCGGGGCGGGCAGGGTATCGGCCAGGCGCTGATGCAGCGGTTGCTGGCCCTGGCCGACCCGACGCGGGAGGTTGTGCTGTCGGCCTCGCTCAACGCCGTGCCGTTCTACCAGCGGCAGGGCTTCGTCGCCGAGCGCGAGGAACTGTATCCGCATCCCAGTGGCGTGGCATTGGCGTCGGTGAAGATGCGCCGGCCGGGGTGAAATTTCCGGCGCTATCGCGCGTTGATCAACGCGTGGCCAACCACGCGGTCACGCCCTCTGCCGCACGCAGTCCGCTGGCATAGCACGCCGTCAACAGGTAGCCGCCGGTCGGTGCTTCCCAGTCCAGCATCTCTCCGGCGCAGAACACGCCGGGCAAGGCACGCAGCATCAGGCCCTCGTCCAGCGCGTCCAGGCGCACGCCGCCGGCCGTGCTGATCACCTCGGCCATCGGCCGCGGGCGCAGCAGGCGCAGTGGCAGGCGCTTCAACGTGGCGATCACCGCGGCCAGATCGTTGCCGGCATCCTTGCCCAGTGTTTCGAACACCAGTGCGGTCTTCACTGCGTCCAGTCCAGCCTGGCGACGCAGGTGCTCGCCGAAGCTTCGCCCCTTGCGCGGCTGCGAAAGGTCGGCCAGCAGCCGTGCCTCGTCGCGGCCCGGAACCAGGTCCAGCCACAGCGTGGCGTGGCCGTCGCGGTTGAGGGTTTCGCGCAGGTCGGCCGACAGGGCGTAGATCAAGCTGCCTTCGATACCGTACTCGCTGGCCACGCACTCCCCTTGCAGGGTGTGCGGCTCACCGTCGAGGCCATGCCAATGTGCGACGACCGGCTTCAGTGGTGCGCCAGCATGGCGTTGCGCGAAGAACGGCGTCCATGCAACGTCGAATCCGCAGTTGGCCGATTGCAGCGGCGCGATGTCCACGGCGCGGGCCTGCAACGCCGGAACCCAGGCACCGTCACTGCCCAGCTGCGGCCAGCTTCCGCCGCCCAGTGCCAGTACGGTCGCATCGGCGCGCACCTCCAGTTCGCCGTTGTCGGTGGCAAAACGCAGTGCGCCGACGTCGCTCCAGCCCAGCCAGCGATGGTTGACGTGCAGGCGCACGCCCTGTTCCTTCAGCCGGCGGACCCAGCCGCGCAGCAACGGTGCCGCCTTGCGGTCGACCGGGAACACCCGGCCGGAACTGCCGACGTAGGTCTCCACGCCGAAGCCAGCGGCCCAGTCGCGCAGCGCCTGCGCGTCGAAACCATCCAGCCAGCGGCCGACGCGGGTTGCCTGCTCGCGGTAGCGGCTGTCGAACAGTGGACGTGGGTCGGAATGGGTGAGGTTGAGCCCACCTTTGCCGGCGATCAGGAATTTGCGGCCCGGCGAGCCCTTGGCCTCGTACAGATCGACATCCAGGCCTGCCGCGCGCAGCCGCTCGGCGGCAAACAACCCGGCCGGGCCGCCGCCGATGACGGCGATGCGGCGCGGCGGGCGGACGTCACTGTTGGACATTGAGCAGCTCGACGTCGAACACCAGCGACGAACCTGCCGGAATCGGGCCGACCTGGCGGTCGCCATAGCCGAATTCCGGCGGAATCATCAGCGTGCGCTTGCCGCCGACCTTCATGCCGGCGACGCCTTCATCCCAGCCACGGATGACCTGGCCCGCACCCAGCGTGAAGGTGAACGGCTCGCCGCGCTCGACCGAACTGTCGAAGGTCTTGCCGTGCTTGTTGTCGGCGCGCTCGTCGTAGATCCAGCCGGTGTAATGCACGCTGACCTTCTGGCCCGGCACGGCCTCGGCACCGCTGCCCGGCTGGGTGTCGATGCGCTCGAACGTGGCAATGGTGCCTCCCGGCGGCGGGCCGGACGGCTCCGACGAGCAACCAACGGCGGCGAGGGACAGCAGCAGGGGAAGCAGCAGGCGGCGCATCAGGCGTCTCCAGGGGCGATGAGTCGAGGGCGGCAAGGTTAGCGCATCGGCGCCGGGTATCATGGTGGCATGGCAAAACTCCTGCTCAATCTGCGCAATGTCGGCAACGACGAATATGCCGATGTCTGCACGCTGCTGGACCAGCACGGCATCGCCTGGTACCGCACCGAACCCAGTCCGTGGGGCATCTCCAATGGTGGCCTGTGGCTGCGCGAGGATGCCGACCAGCCGCGTGCCAAGGCGCTGATGGCCGACTACCAGGCGGCCCGTGGCGTGCGGGTCCGTGCCGAGCGCGAACAGGCCCTGCGCGACGGCACTGCCGAGACCTTTGGCAGCCTGTTGCGCCGCCGCCCTGTGTTCGTGGTGCTGGTGCTGCTGGGCATGGCGGTGGCGGCGGCACTGGTGCTGCTGCCGTTCATGCTGCTGCGGGGGTAGAGGGTTCGGCCGGGTTGCACCCGGCACCCGCAGAGGCAACGGCAACAGCAACAGCGGGCGTTCCGTGGTGGGCGGGGCGGTATAGGCAGGCGGGACACGCCGTAGACCCATCCTTGGGGGCTCGATGGCGCCATCCATGGCGCCAACGGTCCCGCCTGCCCACACCGCCCCGCCCCGGACGCGTTCCGGGTGCTGTCGGTAGATGTCGACCTTGGTCGACACTGTGGTAGATCCACGCCATGCGTGGATGAACGGTGGAGGCTGATGCGGGGGCGGTCAGGCGCTAAAATGGCGGGATGATCGCCAATACCGCTGCCTATCATTTCGCCGTCATCGACGCCCCCCAGGCCCTGTGCGACCAGCTGCAGGCGCGTGCCGAGGCGTCCGGCCTGCAGGGGACGATCCTGGTGGCGGGCGAGGGGCTGAACCTGTTCCTGGCGGGTGCGCCGTCCGCGATCGATGGCTTCTACGCGGAACTGCGTGCTGATGCGCGCTTCGCCGATATGCGGGTCAAGACCAGCTTCAGCGAGCACCAGCCGTTCGCGCGGCTGAAGGCCAAGGTCAAGGACGAGATCATCAGCTTCCGTCGTGACGATGGCCAGCCGCTGGACTACCCGCGCGCGCCGGCCATCGATCCTGCCACCGTGCAGCGTTGGCTGCGGCAGGGGCATGATGATGCTGGCAAGCGCGTGGTGATGCTCGATACGCGCAACCTGCAGGAGATCGAGTACGGCACCTTCAAGGATGCGCTGGTACTGCCCATCCACAAGTTCACCGATCTGCCCGAGGCGCTGGCGCCCCATCGTGAAGCGCTGAAGGACAGCACCGTGGTCAGTTTCTGCACCGGTGGCATCCGCTGCGAGAAGGCAGCGCTGTGGATGCTCAACGACGGCATGGACAACGTGCTGCAGCTCGATGGCGGCATCCTCGGTTACTTCGAGGAAGTGGGCGGTGAGGGCTACGAAGGTCGTTGTTTTGTGTTCGACGAACGGGTGGCGCTGGATGCCGAACTGAAGCCGTTGGTGGACGAGCCGTTGCCCGAGCCACGCCCCAGCGCGTTCTGACCCTTCCACATTGGCCTGCGGGCCTGAACCGGCCAGGCAGGAATCAGCGTCCCGCCACCGGCACTGGCCGTGGGGGCAGGGCGACCCCATCAAACGGGGATCTTGTGACGGAAAACCGCCTGATGATCCCGTTGTCGATTCTCGACCTGGCCCCGGTCTGCGAGGGCAGCGATACCACTGCCGCCTTTGCCAACATGCTTGAGTTCGCCCAGCATGCCGATGCGCTGGGCTACCGCCGCTACTGGCTTGCCGAACACCACAACATGCCTGGCATCGCCAGTGCCGCCACGGCGGTGCTGATCGGCCATGTGGCCGGTGGCACCCAACGCATCCGCGTCGGCGCCGGCGGCATCATGCTGCCCAACCATGCGCCGCTGCAGGTGGCCGAGCAGTTCGGCACCCTGGCCTCGCTGTACCCGGATCGCATCGACCTCGGCCTGGGCCGCGCACCGGGTACCGACCAGCCGACCGCGCGCGCCCTGCGCCGCTATTTCGACAGCGCCGACCAGTTTCCGCAGGACGTACGCGAGCTGCTGCACTACTTCGAACCGGTGCAGCCTGGGCAGGCGGTGCAGGCCGTACCGGGTGGCGGCCTGCGGGTGCCGACCTGGATCCTCGGTTCCAGCCTGTTCGGCGCACGCATGGCCGCCTCGATGGGCCTGCCGTATGCATTCGCCTCGCACTTCGCCCCCGATTCCATGGATGAAGCGCTTGCGGTGTATCGCCGCGAATTCCGCCCTTCGGCCACGCTCAAGCAGCCGCACGCAATGCTGGCGTTGAACGTGGTGGCCAGTGACAGCGAGGCCGAATCGCGGCGGTTGTTCACCAGCCAGCAGCAGAGCTTCGTCAACCTGCGTCGCGGCCGTCCGGGCAAGATTCCGGCGCCGATCGATGACATCGAAGCGTTCTGGGAACCCCACGAGAAGCTCGGCGTGGAGCGGGCGCTGGCGTGCACCGTGCTGGGTGATCCGCAGCAGGTCGCCGATGGCATTGCGGCGTTCGTCGAACGCCATCAGCCCGACGAACTGATGCTTACCGCCAACCTGTACGACCACCGCGCGCGCCTTCGCTCGTTCGAGCTGGCAATGCACGCCTGGCATGCCCGCCACGCGGGCTGAACAATTGCGTCACGGCAATTTGCGGTGCGGACGCGTCTGATGGGGACTCCCACTTCCGGAGTCCCCCATGGACGAATCGCGTACCGAGCACATTGCCCAGCTGGCTGAACTGATCAAGGACGTGGAGGTGGCGATGTTCACCACCCGTGGTGTCGATGGGCGCCTCTACAGCCGTCCGCTCGGCACCCAGCAGGTCGCCTTCGATGGCGACCTGTGGTTCGCCACTGCGGCCGACAGCCCGAAGGTGGCCGAGATCGCGCTCGACCCGCGGGTCAACGTGGCCTATGCCTCGCCATCGAAGAATACGTATGTGTCGGTAGCCGGCGTGGCACGGATCATCGATGACCGCGCGAAGGTCGAAGAGCTGTGGTCGTCGGCGATGAAGCTGTTCTTCCCCGGCGGCCCGGATGACCCGAGCCTGCGCTTGATCCACGTGCGTGCAGAGACCGCCGAGTACTGGGACGGACCGGGCACGCTGCTCGGCTCGGCGTTGAGTTTCGTGTTGTCGGCGGTGCAGGATGAGCCGGCACGGTTGGGCGACAACGGATTCATCGATCTGCGTTGATTGCAGCAACCCGCCGGGCATGGCCCGGCGCTACCGGGCGGGGCTCAGGGTAGCGCCGGGCCATGCCCGGCGAGCGCAGCGGCAGGCGCTCAGAACCAGCGCTGGAACAGGTCGACGGTGTAGCCCACCAGCTGCCCGGAACTGAAGCCGAAGAAAGCGATCGCCACCAGCGCAGCCACCCAGTTGAACAACATCAGCGCGCCGTCGCGTTCAAGCAGGGCCAGCGCGAACAGCAGCAACTGGAAGCCGAACAGATAGTTGGTGAACGGAATCGGCAGCGACAGCAGCAGGCCCAGCAGCACCAGCAGCAGGCCGCTGAAGGCGTGGGCGGGAGCCGGGGTCAGCAGTTGCGGCATGCGCGGCTTGAGCATGCGGTCGAGGCGGCGCAGGGCACCATCGATGCGATCCAGGAACCGGTGCATGGTGCCGCGCTTCGGCCCGCGACGGGCAATGAAGCCGGGCAGCCAGGGCCGGCGCATGCAGAACAGCATCTGCAGGCCGATCAGGATCACCAACGGACCGCTGACTGCGCCGCCCAGCCCCGGGATGGGGATGAAGGCCGGCAGGATGGCGACGAACAGGAATACACCAAAGGCACTCTGCTGCAGATCCTGCAGGATCTGCCCCAGCTTCATGTGCTGGGCCGGGTCACCGAAGGCGAACATCGCCAGCAGGGTCCGGATGCCCTCGTTGCGGTACTCCGGCGATGCAGCGCCGGGGCCGGCGTCAGGCGGTGAGCTCATCGGCCTGCTCGTCGGACAGGGTGCGAAGCAGCAGTTTGTCCACGCGCGCACCGTCCAGATCGACCACCTCGAAGCGCCAGCCGGCCCAGTCGAAGTACTCGCCCGCGTGCGGGATGCGGCCGAAGAAGTGGATGCACATGCCGGCCAGGGTGTAGTAATCGCCATCCTCGGCGTCGGGCAGGTCGTTGCTGCCGATCAGCTCGCGCAGGTCCTCGATCGGCAGCGAGCCGTCCACCAGCAGCGAGCCGTCCTCACGGGTCACCACCAGCGCGTCCTCGTCGGCATTTTCCGTTGCCTGCAGGCGGCCGACCACCGCGCCCATCAAATCGCTGATGGTTACCAGGCCCTGGATCTCGCCGTACTCGTCCACCACCAGCGCCATCGACTGCTGTTCTTCGCGGAAGATCTCCAGCAGCTTCATCGCATGGGTGGATTCGGAGACGTACAGCGGTTCGCGCAACGTCTGGAACAGCGCGTTGTCGCCGCGTGCCATCCGCGTGGCCAGCGATTTCAGCTCAAGCACGCCGACCACGTCCATGTCGTTGTCGCGGTACACCGGGTACCGCGAGAACTCGTGCTCGGCCATGATCTCCAGGTTCTTGTCCAGGCCACCCAGCGTATCCAGCCAGGCGATCCGGTTGCGCGGGGTCATCAGGCTGTCGGCGGTACGGTCGCCCAGGCGCATCACGCGGTTCATCATGTCGCGCTCGTGGCTGTCGATCACGCCGGCCTCGTGGCTCTCGGCCACCAGCATGCGGATCTCCTCTTCGGTCACCGACGCGACCTCGTCCTTGCCCAGGCCGAACAGGCGCAGCACCAGCTGGGTGGTCTTGGACAGCAGCCAGACGAAGGGGAAGGCCAGCTTGGCCAGCCAGCTCATCGGCAGCGCCACCAGGCCGGCGATGTCCTCCGAGCGGGTCAAGGCCAGTCGCTTGGGCACCAGTTCGCCGAAGATCAGCGTGATGAAGGTGATGAAGGTGACTGCAAGGGCCTTGCCGATGCCGCCGGCGTAGGCGAAGCCCGGCATCAGCCCCTGGATCCAGCCGCCGATGGCTTCACCCAGTGCCTCGCCGCCGAGGAAGCCGGTCAGCACGCCGATCACGGTGATGCCGATCTGGACGGTGGACAGGAAGGCTTCCGGCTTCTCCGACAGCTCCAAGGCCTTGGCCGCGCGCTTGGAGGTGCCGGCCAGCTGCTTCAGCCGGCTCTTGCGCGAGGTCATGACCGACATCTCGGACATGGCAAAGAAGCCGTTCAGCAGAACAAGCGCGAAAACAATCAGGATCATTTCAAACACGGGCATCGTCCCCGGTTGGTGACAGGGAGGGCGGGTGCTTGCGATGGCGGCAGGCGCTCAGGAACGGGGTCCGGCGCGGCGCTGGGGGATAAGGGTCGTCGTCCATAAGGTGCGCCCGAAGGCGCGCTGGCATCTTAGCAAAGGGCCGTGGCTGGGTGGCAAATGCCTGTTCAGTTTTGGGCGTCCCGACCCCCGGGAAGGGGCAGGGATACCCGTGATGGTCATCTAGCCGTCATAATTCGCACTGGTGCCGTCCTTCCCGCGACGGCTGACAGGTTTCTCAATGTTCTCTCTGCAGACCATTTTCGGTTCCGGCAAACAGTTCTACACCCTGCTCGATGAGGCTGCCGTCGCGGCTTCCGATGCCGCCAAGGCACTGCATTCGATGCTGCGCGACGCCGATCGCCAGCCCGCCCTGGATGCCTTCAAGCTGGCGCGTCTGCGCGAACGCGCGGCCTCGGACAAGATCAGCCAGGCGCTGGTGGACAGCTTCATGACCCCGATCGAGCGCGAAGACATCGAAGCGCTGGGCTCGGCCCTGTACAAGATTCCCAAGCAGATCGAGAAGTTCGCCGATCGCTATTCGCTGGCCACCACCCACCTGGAACACATCGACTTCGCGCCGCGCGCGGCGATGCTGGAGCAGGCCGCTGGCGTAGTGGTGGAGATGGTCGCCGACCTGCGCCACATGAACCTGGACCGGATGACCGCGCTCAACGAGCGCCTGCGCTCGCTGGAAAACGAGGCCGACCGTCTGATGCTCGAGCTGTACCGCGACATCTACTCCGGTCGCCTGGACAACCTGCAGATGTTCCTGCTCAAGGAATTCTTCGAGATCCTGGAAAAGGCCATCGACCGCTGCCGCGAGGCCGGTGTGGTGGCGTACCAGATCGTGTTGAAGAACAGCTGACGGGCCGGTACCGATGCTCACCCTAGTCCTGGTGGTGATCCTGGCCGCGCTCGTCTTCGAGTTCATCAACGGCTTCCACGATACCGCCAACTCCATCGCTACCGTGGTGGCAACCAAAGTACTGTCGCCCGGTTGGGCGGTGATGCTTGCCGCCTTCATGAACCTCATCGGTGCCCTGACCGGCACCGCGGTTGCACTGACCATCGCGTCGGGCCTGCTCAACACCAACGTGGTCGACGTGACCCCGCAGGTGATCCTGTGCGCGCTGCTCGGCGGCATCATCTGGAACCTGATCACCTGGTGGAAGGGCCTGCCGTCCTCGTCCTCGCACGCGTTGATCGGTGGCCTGTGCGGCGCCGGCCTGGCTGCGGCCCACAACAACTGGGACGCGCTGATCTGGTCCGAACGGCTCGGCAGCTGGGCGCAGAACAAGGGCCTGCTGTGGAAGGTGTTCGTGCCGATGATCACCTCGCCGATCGCCGGCTTCCTGCTCGGCATCGCAGTGATGGTGCTGTTGTGGGCACTGATCGCAGGCCTGGCCAAGATCGGCGGCGCGATCGGCCGGCTGGCACGTCCGCGCATCGTCAATGCGTTCTTCGGCAAGGCACAGATCGCTTCGGCGGCCTACATGGGCTTTGCCCACGGCCACAACGATGCGCAGAAGACCATGGGCATCATCGCGATGACCCTGATCGGTGCCGAGGCGACCGGCGCGTTGAACGACCTGCCGTCGTGGCTGGCCTTCATGCATCCGGACGCGCACGCCGGCGACGGCATCGCCATGTGGATCGTGCTGACCTGTGCGGTGGTGATGGCCGCCGGTACCGCCTCGGGCGGCTGGAAGATCATCAAGACCCTGGGCCACAAGATGGTCAAGCTGCACCCGATCCACGGCTTCGCTGCGGAAACCAGCTCGGCCACCGTGCTGACCCTGGCGGCGCACTTCGGCATGCCGGTATCGACCACCCACAGCATCTCCACCGCGATCATGGGCGTAGGCTTCGCCAAGAACCCGCGTTCGCTGCGCCTGGGCGTGATCGAACGCATCGTCTGGGCCTGGATCCTGACCATCCCGGCGGCAGGCGGCTGCGCTTACCTGATCCTGAAGCTGTTCGAGCTGCTCGGCTGGACCTGATGCCAGGAGCCTTGGGATCAGAGCCCTTTCCCTGCAGGAAAAGGATCTGACCCCGGAAAACAAAAAGCCCGCCGGATTCCGGCGGGCTTTTTCATTTCATGAAGCATCCGTTATCCACGCATGGCGTGGATCTACCGTGTCGACCAAGGTCGACACCTACCAACAGCAGCAGGAAGTCGACACCCACCAACAGCAGCCGGAACCTGTCGAAGGCGGGGTGGGTCCGGTTGCGGGGGTGTCCGCGGCATGGATGCCGCGGCCAAGCCCCCAAGGGTGAGGGCGCTTTGCTTGCGAGGCACTGCTTCGCAAGCGCCCGAACGCACAGCCGCCAGCGGCTGGGCCGGTCTGGGGGTTTACGGCGTCCCCCGCAACCGGGCCCACCCCGCCAACCCACGGAAAGCCCGCTTTTGACGTTGCCGTTGCCGTTGCCATTGCTGTCCGCGGGTGCCGGGCCGCAGGCCCGGCCGACAATCCCTCAATTGCGCTGGAACAACGCCTGCACATCCCTGCGGAACGCCGCCTGGCTGTCAGCCCGGCTGTAGAACATGTGCCCGCCCGGATAGCTGCGCACCTGCACGCGGTCCGGGTTGCTGCCCATCGTCGGCATCTGGTCCACCGTCAGGATCGAGCCCATGAACGGGCAGGACAGGTCATTCCAGCCGTGCACGATCAGCACCTGCAGATGCGGGTCGATCGCCACGGCCTGGCGCAGCTGGGTCACCGCGCCCTCGCGCAGGTCACCATTGCGATCCCACAGACGGTTCACGTCGTAGTTCAGTGCCTGGTAGCGCGCATCCACCTTCCAGCCGACCTCGCGGGTAACGAAGTCGACCATCGCGGTGGTGGTCGGGGCGATGATGCTGTCCAGCAGCGGATCGTTGGCGCGCTGCTCCGGATCGTTCGGGAACGGATCGAACGCAGTGACGTTGGAATCGTAGCGGCTGCCCAGCGTGCCCTTGTCGCGGAACACCTCACGCAGGTAGGCCTGGGTTTCCAGGCGACCGCCGGCGCGGCGCACGAACTGCGGGTCCAGGCCGGTCAACTCGGCCACCCGGCGCAGCATCGCTTCGGTCGCCTGCGGATCGCTGCGGCCCTTCATCAGCGCGGTGGCGTAGTCGCCGCGGGTGTACTCGACCACCTCGCGCATCGCCGCTTCGGTCAGCTTGCCCTGGCGTTCCAGGTGCGCGGCAGCGATCGACGGCAGGGTCTGCATCCACGCCATCGGCGAGACATCGGCGTTGTCTTCCAGGGTCGGGCTCAGGTAAGGCGACACCAGCACCAGGCCGTTCATCGCCACGCCCAGGCGCGTCTGCAGGAAGTGGGTGATGCGCGGGCCGCGATAGCCGCCATAGCTCTCGCCGGTCAGGTACTTGCGCGAGGCCATGCGCTGGTTGCGCAGCAGCCAGTCGTAGATCGTGCGCGAGAGGTACTCGACATCGGCACTGGGCGTATACAGCTGTTTCTTCGCTTCCTCATCGCCGATGCGGGCGCGGCTGAAGCCGGTACCGACCGGATCGATGAACACCAGGTCGGTGAAGTCCAGCCAGGTGCCGGGATTGTCGTGCAGCTTCGCCGGCGCCGATGCGCTGTCGCCTTCCGAACCGAAGGTCACCACCTTCGGGCCGATGGCGCCCAGGTTGAGGTACACAGAAGATGCGCCGGGGCCGCCATTGAGCGCGAAGGTCACCGGCCGGTCCTTGCCCGGCATCGTGTAGGCGGTGAACACCACATCGGCGATCACCTTGCCCTTCGCATCGCGTACCGGCAGGGTGCCGACGGTGGCGGTGTAGTCGAGGGTGCGCCCAGCCAGGCGCATGCTCTGGCGAGCCGACGCATCGGCCGGCAGGGGAGTGGCTTCGGTCTTTTCTTCTTTCGTTTCGGAGGCGCCGTCAGCAGCAGGCGCGGCCAGCACGCAGGCGGGGGCGATCAGCAGGCCGACGCAGAGCGCGGCAGAGTGCAGCAGAAACTTCATGGCACCGGAACGGCAGCGGAAGGGACCCCGATGCTAGGGCGGGGTGCCGCGCACCGTATGTGTCCAAAGGCATGGGCCGGCTTTGTGGCCTGATCCGGTCAAGCGACGGTGGCTGAGCGCACCGCGTCGTCGGCCAGCAGTCCGTACACGGCCGAGTCGGCCAGTTCACCCTGGATACGCCAACGCTGCCGCAGCAGGCCTTCGCGGTGGAAGCCCAGGCGTTCGAGCACGTGTGCCGAGGCGTGGTTGCGTGGATCGATCTCCGCTTCCACCCGGTGCAGTTGCAGGGTGTTGAACAGATAGGCCAGCACCTGCTGCAGCGCTTCATGCATGTAGCCGTGGCCCTGCCTGCCAGGTGCCAGCAGATAGCCGATTTCCGCGCGCGCCGCATCCCGATCCAGGGCAAACACCACGCATATGCCCAGCAGGGGGCCGTCCACCGATTCGCGCAGGGCCAGCTTCAACTGCGTACCGGTGGCCTGTGCAGCCAGGTCGTCGTCGATCTGCGCGCGTGCTTCGGCCGGACGCGTCCACGCCGGGTGGTTCCACCAGTGCATCACGTCCGGGTCGGACTGCAGGGCGAACAGGGCCGCGGCGTCATCGCGGCGAATGGGGCTCAGCACCAGGCGCGCGCTGTGCAGCGGCAGCCCGGGGAACAGCAGTGAGTTGGCGGGCAATGGGGTCGTCCACGCGGATGAACGCGCATTATGGACCCGCAGGGTTTGCCGATGGCGGCCGATCCAACGGCCCGGTAGTGCCGGCCGCTGGCCGGCAACCCAGGTATCCCGCTGGTTCACGAAAAGCAGCCGGTCAGCGGCCGGCACTACCGGGAATCAGACTTCCAGCGAAGCCAGATCGCCCTTGCTCTCCAGCCAGCCCTTGCGGTCAGACGCGCGCTTCTTGGCCAGCAGCATGTCCATCAGTGAATGGGTCTGCTCGCCATCGTCGATGGTCAACTGCACCAGGCGACGGGTGTCTGGATGGATGGTGGATTCACGCAGCTGCGGCGGATTCATCTCGCCCAGGCCCTTGAAGCGGGTCACGTTGATGGCGCCCTTGATCTTCTCGCGTTCGATCTTGTCCAGCATCGAGCGCTTTTCTTCCTCATCCAGGGCGTAGAACACCTGCTTGCCCACGTCGATGCGGAACAGCGGCGGCATCGCCACGAACACGTGGCCGGCATCGACCAGCGCCGGGAAGTGCTTCAGGAACAGTGCGGTCAGCAGCGTTGCGATATGCAGGCCGTCGGAGTCGGCGTCGGCCAGGATGATCACCTTGCCGTAGCGCAGGCCGCTGATGTCTTCCTTGCCCGGGTCACAGCCGATGGCCACCGCCAGGTTGTGCACTTCCTCCGAGGCCAGCACGCTGTTGGAGGACACTTCCCAGGTGTTGAGGATCTTGCCGCGCAGCGGCAGGATCGCCTGGAAATCCTTGTCGCGGGCCTGCTTGGCGCTGCCGCCTGCCGAGTCGCCCTCGACCAGGAACAGTTCGGTGCGCGACAGGTCCTGGCTGATGCAGTCGGCCAGCTTGCCGGGCAGGGCAGGACCCTGGGTGACCTTCTTGCGGACGACCAGCTTCTCGGTCTTCAGGCGCGCACTGGCGCGCTCGATGGCGATCTGCGCGATCTTCTCGCCCAGCTCTACGTTCTGGTTCAGCAGCAGGCTGAACGCATCGTGCGCGGCGCCTTCGACAAAACCGGCGGCCTGGCGCGAGGACAGGCGTTCCTTGGTCTGGCCGCTGAACTGCGGGTCGGTCATCTTCAGCGACAGCACGAACGACACGCGGTCCCACACGTCTTCCGGGGCCAGCTTGACGCCGCGCGGCAGCAGGTTGCGGAAGTCGCAGAACTCGCGCAGCGCTTCGGTCAGGCCGGTGCGCAGGCCGTTGGCGTGGGTGCCGTGCTGTGCGGTGGGAATCAGGTTGACGTAGCTTTCCTGCACCAGCTCGCCTTCCGGCAGCCAGGCCACAGCCCAGTCCACGATCTCGGTGTCTTTCTTCAGGTTGCCCACGAACAGGTCGGCCGGCAGCGACTCGCGATCGCCCAGCTCCAGCTTCAGGTAATCGCGCAGACCGTCTTCGTAGTACCAGGTGTCGACCTCGCCGGTGGCTTCGTCGGTCAGCTTGACGGTCAGGCCCGGGCACAGCACGGCCTTGGCGCGCAGCAGGTGCTTGAGCGCGCGCACGGCGAACTTGGGCGTATCGAAGTACTTCGGGTCCGGCCAGAAGCGCAGGCGGGTACCGGTGTTCTTCTTGCCGACGGTGCCGACCACTTCCAGCGGCGAGGCGCGGTCGCCGTTGCGGAAGGTGATGCGGTGTTCGGCACCGTCGCGCTTGATGTGGATTTCCACCAGGGTCGACAGCGCATTGACCACGCTGACGCCGACGCCATGCAGGCCGCCGGAGAAGGTGTAGTTGTTGTTGTTGAACTTGCCGCCGGCATGCAGGCGGGTAAGGATCAGCTCGACGCCCGGGATCTTCTCTTCCGGATGGATGTCCACCGGCATGCCGCGGCCGTCATCGCTGACCTCCACGCTGCCGTCCTTGAACAGGGTGATCTCGATCGAGCGGGCATGGCCGGCGAGGGCCTCGTCCACCGAGTTGTCGATCACTTCCTGCGCCAGGTGGTTCGGGCGCGCGGTGTCGGTATACATGCCGGGGCGGCGCTTGACCGGGTCAAGGCCGGACAGGACTTCAATATCGGCGGCGTTATAGCGGGCGTTCATCTGTCTTCGAAAGCGTGGAGCGACGGGCAAGTGTGCGGTCTGGACCGGGAATTTGCACGCCTGCGGTTCAGCCTCGTTGGCGGGGAGGGGGTAAAATGGCAACCGCTGGAACCGAACACCGGCGCCCCCCACATCCGAGCCATACCGCGAGGAGGACTCCATGAAGAAGTTGCTGACCATTGCGATCCTGGCTGCCGCCGCTGTTGCAGTGCCGATGGTGCTGGCGCAGAACGCCGGCCAGCCTGCTCCGCAGCAGGGTGAACAGGCCGACAAGGCGCAGTCCGAAGCCGAGGCCAAGGCCAAGCGCCGCGCGCAGGCCAATGCCGAGATGAAGGCCAAGGGCCAGCCGGTGCCGCAGCAGGAAGAAGAGGAAGAGGCACGCAAGAAGAAGTAATTCTTCTGCCCCTCCGAGGCCCTTGCCACAAGGGTTTCCCCCTCGAACGCCCCGCCCAGCGGGGCGTTTCTTTTTGCCGATGGCGCCATCTGCCCCTTGGGTTGGCGGCCATCTATCTGTAAACTATGGCTTTCCGGGAGTAAGTGCGTGTCCACCATTTGCGAATGGGCTGGCACGGCCAAGCGTGGCCTCCAGCAAAGCGGGTCGCAGGTGACGGTCGAAGTGACCGGCACGGCCGCCCCGACCTCGCAGGGTGGTTCCCCGCTGGCGCATTGCGCTGGCCGGGCCCGCACCTCCCTCGCTGCTCCAGCGAACCGGAAAACCCCCTTTCTGCTCCACGCCCGCCCCCCGGGCAGGCGTGGCGCTGCCGTTTTCCATTTCCAGACAGGATGCTTGCAGCCATGACTCCCTTGATTTTCGTAACCGGCGGCGTGGTGTCCTCGCTCGGCAAAGGTATTGCCGCCGCGTCACTGGCCGCCATTCTCGAAGCGCGTGGCCTGAAGGTCACGATGATGAAGCTCGATCCGTACATCAACGTCGACCCGGGCACCATGAGCCCGTTCCAGCACGGTGAGGTGTATGTCACCGACGACGGCGCCGAAACCGATCTCGACCTGGGACACTACGAGCGCTTCGTGCGCACCCGCCTGAGCCGCAAGAACTCGGTCACCACCGGTCGCATCTATGAGGAAGTGATCCGCAAGGAGCGCCGTGGCGACTACCTGGGCGCGACCGTGCAGGTCATTCCGCACATCACCGACGAGATCCGTCGCTGCATGGACGAAGCCACCGAGGGCTTCGACGTGGCCCTGGTGGAGATCGGCGGCACCGTCGGCGACATCGAATCGCTGCCGTTCCTGGAGGCGATCCGCCAGGTGCGCACCGAGCGTGGCCCGGAAAAGGCACTGTTCATGCACCTCACCCTGGTGCCGTACATCGCTGCGGCGGGTGAGCTGAAGACCAAGCCGACCCAGCACTCGGTGAAGGAACTGCGCTCGATCGGCATCCAGCCGGACGTGCTGCTGTGCCGTTCGGAACAGCCGGTACCGGATTCGGAGCGTCGCAAGATCGCCCAGTTCACCAACGTCTCCGAGCGCGCGGTGATCAGCGTGCCCGACGTCGATGTGCTGTACCGCATTCCGATGGGCCTGCACGCACAGGGCCTGGACGAGATCGTCATCAACCAGCTGAAGCTGGCCGACAAGGCCGGCCCGGCCGACCTGTCGATGTGGGAAGACGCCGTCGATGCCACCTTGCATCCGCTGGATGCGGTGACCATCGCGGTGGTCGGCAAGTACATCGACCACCAGGACGCCTACAAGTCGGTCGGCGAAGCGCTCAAGCACGGTGGCCTGCGCCAGCGCACCAAGGTCACCCTGAAGTGGCTGGAAGCGCAGGACCTGGAAGGCAGCGACATGTCCGCGCTGGCCGATGTCGACGGCATCCTGGTGCCGGGTGGTTTCGGCGACCGTGGCTTCGAAGGCAAGGTGCTCACCTCGCAGTACGCCCGTGAGCACAAGGTGCCGTACTTCGGCATCTGCTACGGCATGCAGGCTGCGGTGGTCGACTACGCGCGCCACGTGGTGGGCCTGGAAGACGCCAACAGCACCGAGAACGATCGCCAGTCGCCGAACCCGGTGATCGGCCTGATCACCGAATGGCGCACTGCCACCGGCGACGTGGAAAAGCGTGACGACAAGAGTGACCTGGGCGGCACCATGCGCCTGGGCCTGCAGGAGCAGCGCCTGAAGCCGGGCACGCTGGCCCGCGAACTGTATGGCAAGGACGTGGTCGCCGAGCGCCACCGCCACCGTTACGAGTTCAACAACCGCTACCGCACCCAGCTGGAAGACGCCGGCCTGGTGATCGCCGGCAAGTCGATGGACGACACCCTGGTGGAAGTGGTTGAACTGCCGCGCGACCAGCATCCGTGGTTCCTGGCCTGCCAGGCGCACCCGGAATTCCTGTCCACCCCGCGTGACGGCCACCCGCTGTTCATTGGCTTCATCCGTGCCGCGCGCGAGCGCAAGGCCGGTGGCAAGCTGCTGCAGGAAGTGCGCGCCTGACTTGTCATGGGGGCCGCCGGCCCCCATCTTGCTCGCTTCAACCCCAGCGCACCGGCACTGCCGGTGTAGCGGACAACAAGGAAACGCCATGAAACTGTGTGGATTCGAGGTCGGGCTGGACCAGCCCCTGTTCCTGATCGCCGGCCCCTGCGTGATCGAGTCGATGCAGCTGCAGCTGGATACCGCCGGCAAGCTGAAGGAAGTGACCGACAGGCTCGGTGTGAACTTCATCTTCAAGTCCAGCTTCGACAAGGCCAACCGCACCTCCGGCACGGCCTTCCGTGGCCCGGGCATGGAAGAGGGCCTGAAGGTGCTGGCCGAGGTCAAGAAGCAGATCGGCGTGCCGGTGCTGACCGATGTGCACGAATACACCCCGATGGATGAAGTAGCCTCGGTGGTGGACGTGCTGCAGACCCCGGCGTTCCTGGTCCGCCAGACCGACTTCATCCGCAAGGTGTGCTCGGCCGGCAAGCCGGTCAACATCAAGAAGGGCCAGTTCCTGGCGCCGTGGGACATGAAGCCTGTCGTCGAGAAGGCCAAGGCCACCGGCAACGAGCAGATCATGGTCTGCGAGCGTGGCGCCAGTTTCGGCTACAACAACCTGGTCAGCGACATGCGTTCGCTCGCGGTGATGCGCGATACCGGCTGCCCGGTGGTGTTCGACGCCACCCATTCGGTGCAGTTGCCGGGCGGGCAGGGCACCAGTTCCGGCGGCCAGCGCGAGCATGTGCCGGTGCTGGCGCGTGCCGCTGTTGCCGTGGGCATTTCCGGCCTGTTCGCCGAAACCCATCCGGACCCGTCCAAGGCGCTGTCCGACGGCCCCAACGCGTGGCCGCTGGACCAGATGGAAGCCCTGCTCGAGACCCTGATGGAGCTCGACGCGGTGACCAAGAAGCACGGCTTCTCGCGCTTCGCGTGAGCCAGCACCCGCAGGCGGCGCTGGAGATCCAGCGTCGTCGCCGGCGCTGGCGGCAGTGGCCGTGGGGCCCGATTGCACTCGGCCTGGCATTGCTGTCGGTGTCCGGTGTATTCGCCATCGGCATGCTGTTCGGTGCCGGCATGCGCCCGTCGAGTGCCGGCGGTCCGGTAGTGAACCTGATGCCCTTCGTCATCGCCCTGGCGGTGGCCGAAGTGCTGACCATATCCGCAGGGTTTTTCGCCGCGGTGCTCGGCTGGCGCCTGAACCGGGGCAGGGTTACCGCTGCGCTGGCGATGGTCGTGCTGTCGCTGTGGGTGGGCATCCTGCTGCACGATCTTCTTTGATGAATACGATGCCTGAACCCTCGCGCAGCTGGCCGTGGGGCCTGATCGCCCTGTTGATGTCGGTGCTCGCCTGGGGCGGCTTGCTCGTGGGCGTGCTGGCCTTCGCCGCCAGCTTCCGTCCGCCGGGGGATGGCAGCAACGGCGTGCAGGCCACGCAGTACTGGATGCTGGGCGCGCTGGTCACGCTGGTGCTGTCCTTCGTGGGCAGCCTGGTGGCGATGGTGATGGCCTGGCGACGTCGGCGCGGGCCGGTGTGCGCGGCCATTGCCGGTGCCCTGCTGGTGATGCTGGTGTCGCTGCTGCTGATCGTGATCGGGTCCAGCTGGGGCTGATGCCCATCACGCCATTTGGCAAGTGAGGGGTAGCCGGGGATAATCACGCGGCATTCGCTTTTGTCGCCCCCTCTCCAAACAGGTAACCGGCCCGACCATGAGTACGATCCGCAGCATCCATGCCCGTGAAATCCTCGACAGCCGTGGCAACCCCACGCTGGAAGCCGAAGTCACCCTGGAGGACGGTTCGTTCGGTCGCGCCGCGGTTCCCTCCGGCGCATCGACCGGCACCAAGGAAGCGGTGGAGCTGCGTGACGGCGACAAGACCCGTTACCTCGGCAAGGGCGTGCGCAAGGCCGTCGACAACGTCAACGGCGCCATCGCCAACGCACTGAAGGGCTTCGAGGCTACCGACCAGGCCGGCCTGGACCGTCGCCTGATCGATCTGGATGGCACCGAGAACAAGGGCCGCCTGGGTGCCAACGCACTGCTGGGTGTTTCCATGGCCGCCGCGCACGCCGCCGCTGCCTCCAGCAAGCAGGCACTGTGGCAGTACCTGGCCGGCAAGACCGGCGCGACCCCGTCGCTGCCGGTGCCGATGATGAACATCATCAACGGCGGCGCGCACGCCGACAACAACGTCGATTTCCAGGAGTTCATGGTGCTGCCGGTCGGCTTCACCTCGTTCTCCGAAGCGCTGCGTGCCGGTACCGAAATCTTCCATTCGCTGAAGTCGGTGCTGAAGGGCCACGGCCTGAGCACGGCGGTGGGCGACGAAGGCGGCTTCGCGCCGGACTTCCGCAGCAACGTCGAAGCGCTGGACACCATCCTCGAAGCCATCGGCAAGGCCGGCTACACCGCCGGTGAAGACGTGCTGCTGGGCCTGGACGTGGCCTCCAGCGAATTCTTCGAGAACGGCAAGTACAACCTGGTCGGCGAGAACAAGCGACTGACCTCCGAGCAGTTCGTCGACTTCCTGGCTGACTGGGCCGCGCAGTACCCGATCATCACCATCGAAGACGGCCTGGCCGAGAACGACTGGGCGGGCTGGAAGCTGCTGACCGATCGCATCGGCAAGAAGGTGCAGCTGGTCGGCGACGATCTGTTCGTCACCAATCCGAAGATCTTCCAGGAAGGCATTGATTCGGGCACCGCCAACGCGATCCTGATCAAGGTCAACCAGATCGGTACCCTCAGCGAAACGCTGGAAGCGATCGCCATGGCCGACCGTGCCGGTTACGCCGCCGTGGTCTCGCACCGTTCGGGTGAAACCGAGGACACCACCATCGCCGACATTGCGGTGGCGACCACCGCCACCCAGATCAAGACCGGCTCGCTGTGCCGCAGCGATCGCGTGGCCAAGTACAACCAGCTGCTGCGCATCGAGGAAGCCCTCGGCGCCGGCGCGCGTTACGCTGGTCGTGACGCGTTCGTGTCGCTGAAGCGCTGAGCCGATGCGCGACTGGCGCTGGCTGCTGTTGTTGCTGGCCCTGCTGCTGGCATGGCTGCAGTACCGTTTCTGGTTCGGCCCGGGCAATTCGGGTGAAGTGATGATGCTCGAAGCCCAGGTCGCCAACCAGGAGCGGGACAATGACGGTCTGCAGCAGCGCAACGATGCGCTTGCTGCCGAAGTGAAGGACCTCAAGGAAGGCCAGTCCGCCATCGAAGAGCGCGCGCGCAGCGAGCTGGGCATGATCAAGCCCGGCGAGAAGTTCTATCGCGTCGTGGAAGATGCACCGACGCGCCCGGCGCAGCCTGCGCCGGTTGCGGCCCCGGCCGGTGACCATCCGGCGGACGTGCCATGAGCGCGGCGATCTGGGTGGTTGTTCCGGCCGCAGGGCGCGGCACGCGTTTTGGTGCGCCGTTGCCCAAGCAGTACCTGCAGGCGGGCGGGCAGACCCTGCTCGCCCACACCCTGGACGCACTGCTGGCGCACCCGGCCGTGGCCGGGGCGATGGTGGTGATCGGTGCGGACGATGCCGACTGGCCGGGCTGGAGCGAATGGGCCGGAAAGCCGGTGCTGACCTGCACCGGTGGCGCCACCCGCGCCGCCTCGGTGCTGGCGGGGCTGCAGGCCCTGCCGGACAGCGTGCGTGCCGATGAATTCGTGCTGGTGCATGACGCGGCGCGTCCGAACCTGTCGCAGGCCGATCTTGGCCGCCTGCTGGAAGTGGGCCGCACCGATCCGGTCGGCGCCATCCTGGCTGCGCCGGTACGCGACACGCTCAAGCGTGCTGGTGATGATGGTGGCATCGACGGCACCGAGCCACGTGAGCGCCTGTGGCGTGCACTGACGCCGCAGCTGTTCCGCCGCCACCAGTTGATCCGCGCACTGTCCGAGGCCGCTGCCGCCGGTGTCGATGTGACCGACGATGCCATGGCCATGGAGCGCCAGGGCCAGCGCCCGCTGCTGGTGGAAGGCAGCGAGGACAACTTCAAGGTCACCACGCCGGCCGATCTCGATCGTTTCGAATTCGTACTCTCCCGCCGCGCCGGCTGACCGCCCGCGCGGCCCTGCTGCAAGGGCTGCATCCATGAGCACCTCCCCGTTCCCGCCCGTCCGTATCGGCCAGGGCTACGACGTCCATGCCTTCGGTGAAGGCGACCACATCATGCTCGGTGGCATCGCGGTGCCGCACAGCTGCGGCGTGCTTGCGCACAGCGACGGCGACGTCATCCTGCACGCGTTGTGCGACGCCATGCTCGGTGCGATCGCGCTGGGCGACATCGGCCAGCACTTCCCGCCCACTGACGACCGCTGGAAGGGCGCGGACAGCAGCGAATTCGTGCGCCATTGCGATGGCCTGCTGCGCGAGCGCGGCTGGCGTGTCGGCAACACCGACATCACCGTGATCTGCGAACGGCCCAAGGTCGGCCCGCATGCGCTGGCCATGCGCGAGCGCATCGGTGAACTGTTGCAGCTGCCGTTGGATGCGGTGAGCGTCAAGGCCACCACGTCCGAGAAGCTGGGCTTCACCGGCCGTGGCGAAGGCATCGCTGCGCAGGCGGTCGTGCTGCTGGTGGCCGCATGATCCCGTTGCCGCTCGCGTTCGGTGCACCGCTGCTGCAGGCGCGCATCCGCACCACGCCGGAAGATTTCCAGGTCGATGAGCTGCCCGCTTTCGAAGCGACCGGTGAAGGCGAGCATCTGCTGCTGCATATCCGCAAGCGTGGCGCCAATACGGTGCACGTGGCCAAGGTACTGGCCAAGTGGGCAGGCCTGCCGGAAATGGCGGTCAGTTATGCCGGCATGAAGGATCGCAACGCGGTCACCACCCAGCGTTTCAGCGTACATCTGCCCAAGCGCGTCGCGCCCGATCTGGCCGAGCTGGCCAGTGACGAGATCGAGGTGATCGACTCCACCTGGCACAACCGCAAGCTGCAGCGCGGTGCGTTGGCGGGCAACCGCTTCAGGCTGGTGCTGCGCGATGTGCAGGGTGACGCGGCGGCAATCGACGAGCGCCTGCAGCAGATCGCCGCGCGTGGCCTGCCGAACTGGTTCGGCGAGCAGCGCTTCGGTCGCGATGGCGGCAACGTTCCCGCTGCGTTGGCGATGTTCGGTGGCCGGCGCATGCGCAAGGACCAGCGTTCGCTGCTGTTGTCGGCGGCGCGTTCGGCCTTGTTCAACCGCGTGCTCGCTGCACGCGTGGAGCAGGGCAGCTGGGACCAGCCGCTGCAGGGCGAAGTGTGGATGCTTGATGGCAGCCGCAGCGTGTTCGGCCCCGAGCCCTACAGCGACGTGCTGGCCGAGCGCCTGGCACGTTTCGACATCCACCCCAGTGCTCCGTTGTGGGGCGAGGGTGAGCTGCGCAGCAGCGACGCCGCCCGTGAGCTGGAACTGGCAGCGCTGGATGATGACGAATCAAAGGCGCTGCGCACCGGCCTCGAAGAGGCGCGGCTGAAGCAGGAGCGGCGCGCGCTGCGGCTGCGTCCGGCGCTGCTGCAGCACCAGTGGCTGGCCGCTGACGTACTGGAGTTGTCCTTCGCGCTGCCGCCAGGCTGCTATGCCACTGCGGTCCTGCACGAGCTCGGCCCGGTCGGAGACGCGTCGCAGGCCTGA

Protein sequences of DBSCAN-SWA_3

>NZ_CP040429|1645080:1705758|1678924_1679947_+|WP_080278357.1|DBSCAN-SWA
MRARGRRWIGCSAVLGLMLAIGPVAAQQGPAPTGAVVDMATVQVTGEQPGPGLWKVTAPQGNVLWILGTVSPLPSGVQWRSDEVERTIASVDHVLGDPGFALDAKIGVFKGLTLLPLALKTARDPQGRTLDQILPPATHARWLGLKQTYLGNDRGVEKDRPLVASGRLYQAFLKRNGLRDGKQVKEALGRAYKAHDLKPEDVQVKLKVDDIRGTLKELQATEVDDRACFERTLDTVEFQAPVLRERANAWALGDVAALRRLSGSAMAQTCRELLQDSAFVRRRGWSDMPQQVRTRWLQGVDAALSRHPGTFATVPVSLLLGEGYLDALVQRGYQVESPPE
>NZ_CP040429|1645080:1705758|1674249_1674864_+|WP_154879922.1|DBSCAN-SWA
MSILNVLLSPDQLLVAVDTLAEDAFTGEASTGAKLLLIPQHNLVLAARGSTQFFLRMYELSLQASFRADFTMEQLMRELGLVIDKLWPAYERAAIDAGLPRSVLGTELVLGGWSSKSGRMVATAYAKHDSAASAIVQPLDGGLASPGEPLEGRPDSFELVDVLHAGRLQSAWLNQAVGRQVAGGRLLVASLGERQAVVQDLGAL
>NZ_CP040429|1645080:1705758|1645080_1646517_+|WP_154879863.1|DBSCAN-SWA
MIRHDEDAQTFNLDAEMAVLAGLLLDNDELANVQDWLAPTDFYSPDHARIYECVLELCGENKRADAITAGEWLLDKGGEDGRHLQALAYEISGSAYTRSNVVPYAEVVVEHSRMRSFIATCERALQAAKSRRGYSAEQLASHLSTQMADIAPVRAVGPRPYREVVKKFAAQLRDRHLNGTPIGLPTPWADINKAIGGLRDGQVIVIAARSNMGKSLMGFQLARFTGLRGDHVVEFSMEMVDTDVVARDVAAIGEIPLQWLVGNGDEVSADDSDLYWGKAVPTMQSLMEATVLVDDDPQLSAPQIVARAKRAHRRKPLRLVVVDHLHEMALPGKQDEALERGQALRDLKGLAKFLNCPVVVLAQLNRAGAKGDRPKVTDIRGSGGIEEVADVILFVHRPDAYKPEDRPGLVEVIVGKGRNIQTGTVVALRNEFQYQRAVDWDGPAYEFAAEPEQTKKRKAQLAPRLGIRGRNSQGADNE
>NZ_CP040429|1645080:1705758|1673912_1674188_-|WP_154879920.1|DBSCAN-SWA
MSTEITEILDRLHACEAGLEVHRGYLKAMEYALRVSFLTHQDPSALLDTWTRLLPSIASTHANDEGPLFVAAFQQSLTILTEQIGLDRDAP
>NZ_CP040429|1645080:1705758|1675970_1677533_-|WP_154879927.1|DBSCAN-SWA
MYRGRQQSIKDAEKITYNKEEFMSLGKALEPKINSTDPWSNDPLSRIEQGKILASLISGLNDAPFVISLKGGWGTGKSIFLKRFGYHLEGSHKIPVIRIDAWHSDYLDDPLLAMTSALADRLKDTQSKTSKAADVIIGGLAESAAKIALPALSILAGLVPGGSIAVDVADKLPDIAQNFLDWDRSRRSAEESFRENLSKARERLTKHLKSNDASPIVIIVDELDRCRPDFAIKFLERVKHFFNVKGICFLIATDHKNLPQAVKTLYGQEVDGELYLRKFFDFEFNLPHPSLAHHANQIFQNFPGTDPAEDAEQLRRRLLKISEIEAYDALRDLSPANLDRAEYSIFFAYVASSFGMQLRDSVQAHTLLMAFVRSHPAGQFRFPAIDCLISCLRFAAPQEYAKLVETSTEDLADAVRALSKRMLATVVAINHFLNAKKESEAQDFRNAVLRSMHAAYNNNRQLKDIDFLAHCSLSVRCVEASTRGVNLRLRFNANDYLASVIHLTAAFTELPNLEVGTGKP
>NZ_CP040429|1645080:1705758|1649456_1649945_+|WP_154879871.1|DBSCAN-SWA
MTQITPQQAGGVNVVAFLDMLAWSEGTDNGKQPTKDRGYDVIVGGQLFKSYADHPRVLVDLPKLKIQSTAAGRYQLLRRYYDAYKKTLGLKDFSPLSQDLIALQQIRERRALPLIQAGKVEEAIKAVRKTWASLPGAGYGQHEHKLADLLAVYRKAGGTVAP
>NZ_CP040429|1645080:1705758|1689012_1689666_-|WP_025878888.1|DBSCAN-SWA
MSSPPDAGPGAASPEYRNEGIRTLLAMFAFGDPAQHMKLGQILQDLQQSAFGVFLFVAILPAFIPIPGLGGAVSGPLVILIGLQMLFCMRRPWLPGFIARRGPKRGTMHRFLDRIDGALRRLDRMLKPRMPQLLTPAPAHAFSGLLLVLLGLLLSLPIPFTNYLFGFQLLLFALALLERDGALMLFNWVAALVAIAFFGFSSGQLVGYTVDLFQRWF
>NZ_CP040429|1645080:1705758|1686472_1687240_+|WP_032976500.1|DBSCAN-SWA
MIANTAAYHFAVIDAPQALCDQLQARAEASGLQGTILVAGEGLNLFLAGAPSAIDGFYAELRADARFADMRVKTSFSEHQPFARLKAKVKDEIISFRRDDGQPLDYPRAPAIDPATVQRWLRQGHDDAGKRVVMLDTRNLQEIEYGTFKDALVLPIHKFTDLPEALAPHREALKDSTVVSFCTGGIRCEKAALWMLNDGMDNVLQLDGGILGYFEEVGGEGYEGRCFVFDERVALDAELKPLVDEPLPEPRPSAF
>NZ_CP040429|1645080:1705758|1658734_1659238_+|WP_154879890.1|DBSCAN-SWA
MSIKANIDFSDAVKGLDSLLEARISLARSMGVAGGQVIRDEVKLRAPVGTEEGGSLRPGSLRDAIYLAYRDGRSTDSLQVYSVSWNAKKAPHGHLVEFGHWQTHAVYKDKDGSWTLGAPLAQPKWVPAKPFVRPGYEASLARAQAAMLERGRERLPELLRKERGGAG
>NZ_CP040429|1645080:1705758|1650393_1650876_+|WP_154879874.1|DBSCAN-SWA
MSVLIRFLRAVWSLVIGAAADALQWLSKPGSKIKVVCAVLAFGCAVSGLTAYEKEQKIRDLSAQVVKVRADWEADAARLQADVDTRDQRLAEVATALRAEAEKLEALKAESAVALQALAGKIEASEKEASTWRGRYEQRPDTCKAALELLDSACPALKGY
>NZ_CP040429|1645080:1705758|1687362_1688358_+|WP_154879939.1|DBSCAN-SWA
MIPLSILDLAPVCEGSDTTAAFANMLEFAQHADALGYRRYWLAEHHNMPGIASAATAVLIGHVAGGTQRIRVGAGGIMLPNHAPLQVAEQFGTLASLYPDRIDLGLGRAPGTDQPTARALRRYFDSADQFPQDVRELLHYFEPVQPGQAVQAVPGGGLRVPTWILGSSLFGARMAASMGLPYAFASHFAPDSMDEALAVYRREFRPSATLKQPHAMLALNVVASDSEAESRRLFTSQQQSFVNLRRGRPGKIPAPIDDIEAFWEPHEKLGVERALACTVLGDPQQVADGIAAFVERHQPDELMLTANLYDHRARLRSFELAMHAWHARHAG
>NZ_CP040429|1645080:1705758|1689649_1690969_-|WP_049464874.1|DBSCAN-SWA
MPVFEMILIVFALVLLNGFFAMSEMSVMTSRKSRLKQLAGTSKRAAKALELSEKPEAFLSTVQIGITVIGVLTGFLGGEALGEAIGGWIQGLMPGFAYAGGIGKALAVTFITFITLIFGELVPKRLALTRSEDIAGLVALPMSWLAKLAFPFVWLLSKTTQLVLRLFGLGKDEVASVTEEEIRMLVAESHEAGVIDSHERDMMNRVMRLGDRTADSLMTPRNRIAWLDTLGGLDKNLEIMAEHEFSRYPVYRDNDMDVVGVLELKSLATRMARGDNALFQTLREPLYVSESTHAMKLLEIFREEQQSMALVVDEYGEIQGLVTISDLMGAVVGRLQATENADEDALVVTREDGSLLVDGSLPIEDLRELIGSNDLPDAEDGDYYTLAGMCIHFFGRIPHAGEYFDWAGWRFEVVDLDGARVDKLLLRTLSDEQADELTA
>NZ_CP040429|1645080:1705758|1680011_1680458_+|WP_080149520.1|DBSCAN-SWA
MPLHAYAYVSTAREGLDVPELDALLADATAFNRMAGVTGALMFDGSRFLQYIEGPRDGLASVHARIGNARRHGSIIQLAAGPIPSRWFPRWTMANRHVDAATLGSIVAAPWHGFSLGQEPPEHGFCLLLRAWTGRHGELEPAAVSLGS
>NZ_CP040429|1645080:1705758|1660320_1660629_+|WP_154879896.1|DBSCAN-SWA
MFKVKAPETIKASLTIVGHGREQKLNLTYRHMTQEAYSAVLGRLAGQEITSTQAILDMVVEWDADVDLDTAGVDEALQQQIGLDAVIITGYAQAIQVARKGN
>NZ_CP040429|1645080:1705758|1677586_1678561_-|WP_154879929.1|integrase|DBSCAN-SWA
MASIQRSGNKWRVQVFVAGVRDSTTKHTKQEAAKWALEREAELRGGKLPDKSLREAMHRYVKEEAPKRAGERWESVRIAAWERSLPLLDRRIAAIDSSDIIAWRDGRLKQVKPGTVAREMNLMRSVFETARREWKWIKQNPMSDVRWPQQPKGRARRVSPTEEADLIAAFGLDKGLSAETATQRTGLAFLLALETAMRSGEILSLTWPNVHLSEQYVHLPKTKNGDARDVPLSRRACEILKALPLGFGPVFQLKSAVRDALWRKVRDSTGHREVHFHDSRAEAIWRLSKKLDILQLARIIGHRDLKSLMIYYHEPASEIARHLG
>NZ_CP040429|1645080:1705758|1685810_1686176_+|WP_032976499.1|DBSCAN-SWA
MAKLLLNLRNVGNDEYADVCTLLDQHGIAWYRTEPSPWGISNGGLWLREDADQPRAKALMADYQAARGVRVRAEREQALRDGTAETFGSLLRRRPVFVVLVLLGMAVAAALVLLPFMLLRG
>NZ_CP040429|1645080:1705758|1693483_1694980_-|WP_154879944.1|DBSCAN-SWA
MKFLLHSAALCVGLLIAPACVLAAPAADGASETKEEKTEATPLPADASARQSMRLAGRTLDYTATVGTLPVRDAKGKVIADVVFTAYTMPGKDRPVTFALNGGPGASSVYLNLGAIGPKVVTFGSEGDSASAPAKLHDNPGTWLDFTDLVFIDPVGTGFSRARIGDEEAKKQLYTPSADVEYLSRTIYDWLLRNQRMASRKYLTGESYGGYRGPRITHFLQTRLGVAMNGLVLVSPYLSPTLEDNADVSPMAWMQTLPSIAAAHLERQGKLTEAAMREVVEYTRGDYATALMKGRSDPQATEAMLRRVAELTGLDPQFVRRAGGRLETQAYLREVFRDKGTLGSRYDSNVTAFDPFPNDPEQRANDPLLDSIIAPTTTAMVDFVTREVGWKVDARYQALNYDVNRLWDRNGDLREGAVTQLRQAVAIDPHLQVLIVHGWNDLSCPFMGSILTVDQMPTMGSNPDRVQVRSYPGGHMFYSRADSQAAFRRDVQALFQRN
>NZ_CP040429|1645080:1705758|1698498_1700163_+|WP_025878896.1|DBSCAN-SWA
MTPLIFVTGGVVSSLGKGIAAASLAAILEARGLKVTMMKLDPYINVDPGTMSPFQHGEVYVTDDGAETDLDLGHYERFVRTRLSRKNSVTTGRIYEEVIRKERRGDYLGATVQVIPHITDEIRRCMDEATEGFDVALVEIGGTVGDIESLPFLEAIRQVRTERGPEKALFMHLTLVPYIAAAGELKTKPTQHSVKELRSIGIQPDVLLCRSEQPVPDSERRKIAQFTNVSERAVISVPDVDVLYRIPMGLHAQGLDEIVINQLKLADKAGPADLSMWEDAVDATLHPLDAVTIAVVGKYIDHQDAYKSVGEALKHGGLRQRTKVTLKWLEAQDLEGSDMSALADVDGILVPGGFGDRGFEGKVLTSQYAREHKVPYFGICYGMQAAVVDYARHVVGLEDANSTENDRQSPNPVIGLITEWRTATGDVEKRDDKSDLGGTMRLGLQEQRLKPGTLARELYGKDVVAERHRHRYEFNNRYRTQLEDAGLVIAGKSMDDTLVEVVELPRDQHPWFLACQAHPEFLSTPRDGHPLFIGFIRAARERKAGGKLLQEVRA
>NZ_CP040429|1645080:1705758|1684072_1685320_-|WP_154879936.1|DBSCAN-SWA
MSNSDVRPPRRIAVIGGGPAGLFAAERLRAAGLDVDLYEAKGSPGRKFLIAGKGGLNLTHSDPRPLFDSRYREQATRVGRWLDGFDAQALRDWAAGFGVETYVGSSGRVFPVDRKAAPLLRGWVRRLKEQGVRLHVNHRWLGWSDVGALRFATDNGELEVRADATVLALGGGSWPQLGSDGAWVPALQARAVDIAPLQSANCGFDVAWTPFFAQRHAGAPLKPVVAHWHGLDGEPHTLQGECVASEYGIEGSLIYALSADLRETLNRDGHATLWLDLVPGRDEARLLADLSQPRKGRSFGEHLRRQAGLDAVKTALVFETLGKDAGNDLAAVIATLKRLPLRLLRPRPMAEVISTAGGVRLDALDEGLMLRALPGVFCAGEMLDWEAPTGGYLLTACYASGLRAAEGVTAWLATR
>NZ_CP040429|1645080:1705758|1666929_1667670_+|WP_154879910.1|DBSCAN-SWA
MQQTTLQAIQAHAVAEYPRECCGLIVAGADGEAYIPCRNVATTPSEHFRLPAEDFADAEDVGEVLAVVHSHPNASAAASDADRVMCEASRLPWHIVSVGQCVGADPECGDLQTIDPCGYEAPLVGRQFAHGVLDCYSLVRDFYARELGIRLSQYEREDDWWEKGQDLYGLDRLRAEGFELIEGEPQRGDMVLMQIRSPVPNHAGVYLGDGKMLHHMHGRLSETVVYGGMWAERTRHIVRHKETGHD
>NZ_CP040429|1645080:1705758|1671806_1672196_+|WP_154879916.1|DBSCAN-SWA
MADVGLRVRSESGYVETTVTTRLTKIIGSYTFPLYNPVNSNNKWIAPPAANGGLIVNDFSGGEPFYYFTCEGQRSVYGMLVPSVTISGNSINWSWDPDVVNFHVRMEMFPSKPTTDTVGGITLHYGIYS
>NZ_CP040429|1645080:1705758|1675326_1675821_+|WP_154879924.1|DBSCAN-SWA
MLPSHGYQGFRSAPPPSGWVQLRDTWVLWWGGRQIAQISPAKERGVRVHLDARKMWQTKDVWAASVDQGKRYAERWCAARLYPEMRLRAAVARMVDDSLREPLPPLPGLPPTPEQLQQARRLAEAGAKELERVKEALEPRRPLAVTKPMAKDPMKAGVRTARTE
>NZ_CP040429|1645080:1705758|1654419_1655679_+|WP_154879880.1|portal|DBSCAN-SWA
MTTFRWYNPMSWRFFGYDDPATGNYVEVDLSVGGKGTKAGVRVTQKSALTVSIVWSCVKVLSESAAGLPWKLYEDTGGLRALVKGNSAQRRRLLRLMAKPNPYIKWLDLIKAVVVNMALRGNAFAIIQRDDSGAWIGLIPVGVDSVRIDTDDGLIYWATINGKETPVSPENMLHFKLFSPDGIVGLSPVEYQAETIGLARAAQDWSARFMRKGGFTGGYIIYPGFLTKEQQAQIKAKLPDIRQGDVDDLGKMAILQGGPTITPAGLTQKDSQFIESQQFQEEALAGIWGVPLYLTNRARSTSVLGSNLEQQTSGFVTFGLKPYLDAIESEINDKLFAETEIFVEAVVEGLLRADSGARSTYYKTALGGSGGSGWMTINEVRVKENLPALDGDQYNQVTRWTSNQPDSSNDDPTGDPANA
>NZ_CP040429|1645080:1705758|1697863_1698097_+|WP_154879947.1|DBSCAN-SWA
MKKLLTIAILAAAAVAVPMVLAQNAGQPAPQQGEQADKAQSEAEAKAKRRAQANAEMKAKGQPVPQQEEEEEARKKK
>NZ_CP040429|1645080:1705758|1703152_1703503_+|WP_025878900.1|DBSCAN-SWA
MRDWRWLLLLLALLLAWLQYRFWFGPGNSGEVMMLEAQVANQERDNDGLQQRNDALAAEVKDLKEGQSAIEERARSELGMIKPGEKFYRVVEDAPTRPAQPAPVAAPAGDHPADVP
>NZ_CP040429|1645080:1705758|1658079_1658388_+|WP_154879887.1|head,tail|DBSCAN-SWA
MAVTLDLELVRKQCNVVADVDDALLQQYVAAALAHIEQHCDRKLVEGDPSGPDQLKLEADVVQAALLLVGHWVANREAVVIGEVSTAVQFGVERLLWYRKAF
>NZ_CP040429|1645080:1705758|1680569_1681856_+|WP_154879932.1|DBSCAN-SWA
MSAPIGAAQSPSPAIIGLGYVGLPLAVAFGRQLPTLGYDIDAARIAELAGGQDHTLEMEPDELVSASLLRYSSDPAQLDACNVYIVTVPTPIDAYEQPDLEPLRSATRLIASHLRVGDLVIYESTVYPGTTEEVCVPLLEQGSGLRFNEDFYCGYSPERVSPGDRQRRLADIRKITSGSTPDVAAVVDGLYQRIITAGTFPVPSMRVAEAAKVVENIQRDVNIALVNELALIFDRLGIDTQDVLDAAGSKWNFLPFRPGLVGGHCIGVDPYYLLHKSESMGYHPDLIHTARQVNNRVGEHVAKRVLAMLAERGRMPAHSRILVLGVTFKEDCPDLRNSRALELAQRLAGSGAQLDVSDPWVGPAAMADEGVNWLAEPVPGSYDAVVLAVAHESFKAMDDAHIRSLLAPGGLVYDVKSAWPRSVVDDRL
>NZ_CP040429|1645080:1705758|1664559_1665672_+|WP_154879904.1|DBSCAN-SWA
MARQIIDTDTQNPGWVGDIAKIAFTKANENFGELYAVLGSGGVIDARIPAKNLLINGNMRVLQRGSSGTLNNTEVFGPDRWKIGCLGGVTCNWGVGQAPAGTLRNSRFFLGYNVVAGASAWIGQKVEGVLTIHGDKATFSFLMRSTPAGRKVGIRIIQDFGTGGSPSGQVVTEVGVVTLGGAFEPHSVTFDVPSAAGKTFGSSGTDHLYLLIDFSGSGHGGQISGQTGLFEFSEAQLERGSKATAFEHVAMADEVERCQRYFQKSYDLNIVPGTANATAGQDTFFFYGDPNSGRAVGMTSRFATRMRGIPAVTIYSPATGAAGQVRSEAPAGDYVGGVNTPGQSGFFLTTVAITTNNTNVRWQWAADAEL
>NZ_CP040429|1645080:1705758|1701855_1703148_+|WP_032976506.1|DBSCAN-SWA
MSTIRSIHAREILDSRGNPTLEAEVTLEDGSFGRAAVPSGASTGTKEAVELRDGDKTRYLGKGVRKAVDNVNGAIANALKGFEATDQAGLDRRLIDLDGTENKGRLGANALLGVSMAAAHAAAASSKQALWQYLAGKTGATPSLPVPMMNIINGGAHADNNVDFQEFMVLPVGFTSFSEALRAGTEIFHSLKSVLKGHGLSTAVGDEGGFAPDFRSNVEALDTILEAIGKAGYTAGEDVLLGLDVASSEFFENGKYNLVGENKRLTSEQFVDFLADWAAQYPIITIEDGLAENDWAGWKLLTDRIGKKVQLVGDDLFVTNPKIFQEGIDSGTANAILIKVNQIGTLSETLEAIAMADRAGYAAVVSHRSGETEDTTIADIAVATTATQIKTGSLCRSDRVAKYNQLLRIEEALGAGARYAGRDAFVSLKR
>NZ_CP040429|1645080:1705758|1672983_1673916_+|WP_154881324.1|DBSCAN-SWA
MCYSAQIEAAYQKLVRMTGATVSLQEFAALYAHDPGKKRPKTPKAMDDAFRAGTSPAERAVWAEIQQWNQAEATILEQELFANRKRLADAERSLQAKETKKAREDVRIAGKKIERAMGKLADLKRTEGKDRDSRIFPGVYAPVLVSDGGKLTIKPMRYQCRLAGKPANYDQRFPGTYNARRDSLEKFWAPAFGHTHGLMVVDTFYENVEGPDGKNQVVQFTPRTREPMLVACLWSHWVDPAGKEPDLLSFAAITDDPEPEVAAAGHDRTIINIKPEHVDAWLNPDPADLAALYRIFDDKRHPFYEHRLAA
>NZ_CP040429|1645080:1705758|1672195_1672933_+|WP_154879918.1|DBSCAN-SWA
MAVGLRVRNQGTGQIQIGLGYRNLQLAKSGTLNTGSFSGGGTGGSPPFASWSPSGVLASTNGTTNLHVCRYINDSVATTTGFTLVQTGVTCFVYASSQAPNKTLEYYTFNATERAASGPVGLRMRGEDGTVFYDSRRKGLRVLQVVALPTVPGPPVEIGQFFPGTKIGIAIPSPRFYYFAQSQDRCTMNADYFHMTSDNRIFLSRLQVTQQTLITNTFPVGGVTMGPQNASIFIVDLTEVPLGFG
>NZ_CP040429|1645080:1705758|1665674_1666148_+|WP_154879906.1|DBSCAN-SWA
MYRYTHDPDLLVCLETGATIPRGNYLWPGDWLASGGVPEPIAPPYVLYSPEHFRAIRDAAFAWMEAEVKGRGYDSIANCTSYFNSGVERYRLEARAMVAWRDDVNQALERLVVSPPEGIETWDQVRTLLPQPIAYEWPATVELPLDAGESAPPVVMS
>NZ_CP040429|1645080:1705758|1703499_1704198_+|WP_032976507.1|DBSCAN-SWA
MSAAIWVVVPAAGRGTRFGAPLPKQYLQAGGQTLLAHTLDALLAHPAVAGAMVVIGADDADWPGWSEWAGKPVLTCTGGATRAASVLAGLQALPDSVRADEFVLVHDAARPNLSQADLGRLLEVGRTDPVGAILAAPVRDTLKRAGDDGGIDGTEPRERLWRALTPQLFRRHQLIRALSEAAAAGVDVTDDAMAMERQGQRPLLVEGSEDNFKVTTPADLDRFEFVLSRRAG
>NZ_CP040429|1645080:1705758|1700251_1701082_+|WP_012510652.1|DBSCAN-SWA
MKLCGFEVGLDQPLFLIAGPCVIESMQLQLDTAGKLKEVTDRLGVNFIFKSSFDKANRTSGTAFRGPGMEEGLKVLAEVKKQIGVPVLTDVHEYTPMDEVASVVDVLQTPAFLVRQTDFIRKVCSAGKPVNIKKGQFLAPWDMKPVVEKAKATGNEQIMVCERGASFGYNNLVSDMRSLAVMRDTGCPVVFDATHSVQLPGGQGTSSGGQREHVPVLARAAVAVGISGLFAETHPDPSKALSDGPNAWPLDQMEALLETLMELDAVTKKHGFSRFA
>NZ_CP040429|1645080:1705758|1646727_1647273_+|WP_154879865.1|DBSCAN-SWA
MSLSLKEQLKHWGHYQEHRFCAPLAPEEAPSRGEHPLARAQQFAQGTKRERPPLLRDGHDRRMLLGAGAGRVNRNGAVLPVAPWAVDPIPCTETRTLVSRSATAAVMVGSPEEYRWIDRALSDLYRQNMVRALVVLEEFTGRGSQAQRAAAVAKKLGAEFTKWQYRKELDKGMAFMEAARR
>NZ_CP040429|1645080:1705758|1664220_1664550_+|WP_154879902.1|tail|DBSCAN-SWA
MTDTFHWQATSQSSGTATASVRRAKFGDGYSQQVAEGINSVSRKYQLSFVASKAVIAEIVAFLDTHVGASFLWASPWGTGLYYCDTYTDSHLGGLTYSVTATFEQTFQP
>NZ_CP040429|1645080:1705758|1695078_1695657_-|WP_059063745.1|DBSCAN-SWA
MPANSLLFPGLPLHSARLVLSPIRRDDAAALFALQSDPDVMHWWNHPAWTRPAEARAQIDDDLAAQATGTQLKLALRESVDGPLLGICVVFALDRDAARAEIGYLLAPGRQGHGYMHEALQQVLAYLFNTLQLHRVEAEIDPRNHASAHVLERLGFHREGLLRQRWRIQGELADSAVYGLLADDAVRSATVA
>NZ_CP040429|1645080:1705758|1667662_1668280_+|WP_154879912.1|tail|DBSCAN-SWA
MTERLRTVRLYGRLGARFGRKFQLAVNSPAEAIFALGVLLPGFRQFLTGCRDQGIEFAVFIGRENLSKAQLHDPPGADDIRIAPVLVGSKRGGALQTIVGVALIVVATIYGGPQAGAGVAKFWGAIGAAGWSLAIGGVVQMLSPQPRGLGTKESAENTPSYSMNGPVNVQAQGNPVPVAYGGHDTKGMVVGSVVISGGIYAEDQQ
>NZ_CP040429|1645080:1705758|1661434_1664224_+|WP_154879900.1|tail|DBSCAN-SWA
MWRVFYVRGNVCMTDQSLGAARIDLVVDTQQFDSAISAAKRGVADMSGSAQQQYHQLSRAERSRVDSLVRQADTLGMTRSQQLAYNAALRTSGPVLDEIVQKLARAEAAAKRSGKELNAYGVSAAQQANAMRGVPAQITDIAVSLQGGQNPLTVFLQQGGQLKDMFGGIRPAAAALASQLLALINPLTIAAAVTGGLAFAWYQASEEQGRFQRALVLTGGHAGFTAEQLGEMSRALDSLEGITRGKAAAALAEVAQSGRFAGEQFELVTRAALQMNIATGASIEETIGKFAEFRKDPVKALLDLNRAENFLYQSQLDRIVALRDEGREQDAAAEAMRLYADVVEDRTGKVLNSLGLVATAWKEIKGASGEAWDAITEGAANADRGLKQFADRVANMPRVAQDLTTYGLAMVNLPLAAVVRLGGDRFGGVKGTVDSTAPLAGTIDSDQAEKALKERRKAQEEWERLSGQNLSKRQKQLAEEANIVALGKKLGKDQADIDREVAASRKQFEEAESRRSGGSKSNPATAIVAQIQQQVALNKEQVRSEEKLSVSQRLRVQVMEELDRMGGKIPEADRKRIRTMLEELRATGALVEAKDKQKKTLEALTRQQAIFDQQTESRQRANELDLMGYGRGQDTVAQLRRQMDVQREYEDELKRLGDRQVATDQDQWDQLAANAAKHRDEQLQLETDYQARRLAAMGDWRNGTRAAFEDYATEANNAAGQAHSALTNAFQGAEDALVQFAMTGKLSFRDLANSIIADLARIAAKQAIVGIAGMIAGAWGGAASAGASSGTLQGFGNNTSWLTANANGGVYNTPSLSTYSGGVYSSPQLFAFAKGAGVFGEAGPEAIMPLQRGPDGRLGVAAHGGGSGASQVNVSVVVNSDGSTDVSADTPVWQRFGKEIGQLIDMKINDAQIRSMKDGGAMRVMGGGR
>NZ_CP040429|1645080:1705758|1647269_1647704_+|WP_154879867.1|DBSCAN-SWA
MRLASTVNSHVIQAAVDAVFLRVVCSANGRVRVGISREPLEGLRKLAGQEAIAAQWAWIGSAAKGKAVERSLRKRWASRYRVGEGFGFDYGTEGRLFRDELDATFGEVVGVLPQWRKVGPEEMAEIIGGMRKERRRPALPVKRN
>NZ_CP040429|1645080:1705758|1652304_1652583_+|WP_154881323.1|DBSCAN-SWA
MTAGEKRAWKEFAAEMPWLNASHRVLLRLACLWTARMEDPKAEFGVSATQALSSILSKLGATPVDESKVSHGGDDEDAGEEFFAGAGSGRSH
>NZ_CP040429|1645080:1705758|1668276_1671807_+|WP_154879914.1|DBSCAN-SWA
MSAFLLPGTHAAVALVSSGILGAGGKSSTNARTPVETPDSLHSISYAKVLDLISEGEIRGLVAGNQSIYLNEVPIQNSDGTFNFNGVRVETRSGTQDQEYIPGFPSVENEIGVGVELRDTPVVRAASGQDLSAVRIRFGVPALQRQNTENGDTEGYAVEYAIDLSTDGGAFSTVLSNAFRGKTTTEYQRSHRIDLPPGNQWQARIRRLTPNANSATVADTVNVISMTEIIDVKLRYPNCAIVAVQTDGSQFQGKPTTAYRIWGRIIRVPSNYDPIARSYTGVWDGTFKSAWTNNPAWVYFDMVTNDRFGLGDRVPLDWVNKWRLYEIAQYCDQLVSDGMGGMEPRFTCSLYLQTRESAHKVLQDMASMFRGISFYAAGQIMASADMPKDPIYTYSQANVVDGKFTYIGSGGKARHTVALVSWSDPDDFGRQKVEPVQLQEGIARYGVNQIEVTAFGCHSKSQAQRVGLHILYSENLETETVNFAVGLDALNCMPGDVIQVANAKRAGRRNSGRISAASASSLTLDVVPTSMQVGDLLRATLPSGKTEARTINGINPGTCVVTVSAPWSAVPVAQSIWATESTDLVMEQFRVISVTEEDGLTYRITGLTHRPDKFAAIDDGTRLEPPPISIVPPSVQPPPANVRMSSHVVIDQGIATPVLTIEWDAADKAIAYDVEWRRDDLNWVRAGRVATASTEVRGIYAGKYLARVRAVNALNAVSQPTLSALTDIQGKTEPPPALTSLTATSVVFGIQLAWAFPPGATDTERTEIWRSAGPNLENATKMGDFAYPQNRFQLDGLAAGAKFYFWGRLVDRSGNIGPWYPAGAGVVGESSTDATLYDTYFSGLINKSALGQELLSEIESISGIVPLIWAADATYEPGQTVIHNGKIWSWKGAGPGNEEPPSANWLNVGDAVAQAGAVVGRVNSLELAVNDPDTGLQAVGRKTDGLFAQLDAQGAGDADWGAGNENVFAGTTTLQTVMVEADRALAKRVDTVEASVGDIDLGGVQASVQQTSQAIVDLNGRISATYTVKAQITSAGQIYMAGMGLGVEQQPDGSYQSQILMQADRFGVINVVNGNVTAPFVIQGGQTFINQALIGTAWITSAKIADAAITNAKISGTIQSDDYVSGQTGWRINKAAGGGFEFNGTVAGGYRLNITNQGIYIRYPNGNLAVELGVLQ
>NZ_CP040429|1645080:1705758|1651155_1651518_+|WP_154879878.1|DBSCAN-SWA
MAQQTERQNRVLALGRLKTGEMNRTEAAYAERLRALQAAGEIQWHRFEGLKLRLADNTFYTPDFAVMAADGVMECHEVKGHWQDDARAKIKIAASMYPFRFIAVKVKAKRDGGGWAVEEF
>NZ_CP040429|1645080:1705758|1659661_1660321_+|WP_154879894.1|tail|DBSCAN-SWA
MALKLPKGTQFGFAQVVSTAIATTGISKAAPALVSVADGAVDTDDVVVLEIPGWPALNNRTTRAGAESTGAIELLGTDTTDTVLYPGTSGAGTLRKAGTFIDLDQQGDPTTAGGEQQYWSGTLLEDPTGRQIQIPTFKNAKTITIPLYYDPSKPWYPALKTVDAKGEPVVMRAKLAGGDVLYWYGYLSYDGDPTMTANTPMGTTATFTALADSILVEAA
>NZ_CP040429|1645080:1705758|1701078_1701426_+|WP_154879949.1|DBSCAN-SWA
MSQHPQAALEIQRRRRRWRQWPWGPIALGLALLSVSGVFAIGMLFGAGMRPSSAGGPVVNLMPFVIALAVAEVLTISAGFFAAVLGWRLNRGRVTAALAMVVLSLWVGILLHDLL
>NZ_CP040429|1645080:1705758|1691246_1691873_+|WP_025878890.1|DBSCAN-SWA
MFSLQTIFGSGKQFYTLLDEAAVAASDAAKALHSMLRDADRQPALDAFKLARLRERAASDKISQALVDSFMTPIEREDIEALGSALYKIPKQIEKFADRYSLATTHLEHIDFAPRAAMLEQAAGVVVEMVADLRHMNLDRMTALNERLRSLENEADRLMLELYRDIYSGRLDNLQMFLLKEFFEILEKAIDRCREAGVVAYQIVLKNS
>NZ_CP040429|1645080:1705758|1683585_1684047_+|WP_025878881.1|DBSCAN-SWA
MQFRTGTDDDVGTLWALRTRCVRELCSSHYPPEVIAPWSASPPPVQYSRLLGQGGCVVAEDDRGNVLGFGVFDTEGNEIDALFVDPDRGGQGIGQALMQRLLALADPTREVVLSASLNAVPFYQRQGFVAEREELYPHPSGVALASVKMRRPG
>NZ_CP040429|1645080:1705758|1701425_1701758_+|WP_105163832.1|DBSCAN-SWA
MNTMPEPSRSWPWGLIALLMSVLAWGGLLVGVLAFAASFRPPGDGSNGVQATQYWMLGALVTLVLSFVGSLVAMVMAWRRRRGPVCAAIAGALLVMLVSLLLIVIGSSWG
>NZ_CP040429|1645080:1705758|1660637_1660937_+|WP_154879898.1|DBSCAN-SWA
MGALYWRAPTEAELAQVGLKAKHYQPPEVQLWPECSLPIEIFSRVSTQWRASAGGPFGLDYNVVFQELDREGLEGDRRAEVMAALRIIEGEAILQINRG
>NZ_CP040429|1645080:1705758|1656315_1657527_+|WP_154879885.1|capsid|DBSCAN-SWA
MPDNIIEIREGLEKQLKDGFAGLQKKYDSASAEIEKGNQVTTDLKKQIQTATDEIQKVVDKVLKLEEKGIGLGNQPGTKKGFIDFIKGNDEYKALQGREKAAAEIEVKKDELASMQETKAVTSAGIVVPNFDPTIQPGIRQELRIRDLIPSISVTGQSYTYFREKLHTRGAGAVGEGTAKPQSNVTFEQKTDLVKKLAVWIPVTDEALDDVPQMYGYLQQLLRYDLKLEEEAQILKGDGLGNNLPGLMTDATLFDDDLSKAGDTSIDTVRRAIYQVRKQSKLSADATVMTELDWMNIELEKDSQNRYLFANLQGFVTPILWGRPVVASDSMDEGDGTTTGGEFLVANFQRGATIYDRMSFLFKVGLINDDFVKNQRVLLVEERLGLAKRRVEAFVKGRFKPQV
>NZ_CP040429|1645080:1705758|1688425_1688923_+|WP_154879941.1|DBSCAN-SWA
MDESRTEHIAQLAELIKDVEVAMFTTRGVDGRLYSRPLGTQQVAFDGDLWFATAADSPKVAEIALDPRVNVAYASPSKNTYVSVAGVARIIDDRAKVEELWSSAMKLFFPGGPDDPSLRLIHVRAETAEYWDGPGTLLGSALSFVLSAVQDEPARLGDNGFIDLR
>NZ_CP040429|1645080:1705758|1666144_1666837_+|WP_154879908.1|tail|DBSCAN-SWA
MITADAQQLEPGARVTVYELDCTSFGADQLFFHAHLQSGSIWWQGQEYGPWPISATGFERTSEQQPNPRLKVSNINGTIAALCRMFQDLAGAKLIRRQTLVKYLDAANFPEGNPLADPGEHFPDEIWYIERKVGEDDETVEFELTTVADFNGRLLPARQCTRICSALLHGGYRGPYCGYTGSAYFDINDQPVSDPARDVCAGLVRSCQLRFGQDKPIPHGGFPAAGLLRT
>NZ_CP040429|1645080:1705758|1704232_1704730_+|WP_025878902.1|DBSCAN-SWA
MSTSPFPPVRIGQGYDVHAFGEGDHIMLGGIAVPHSCGVLAHSDGDVILHALCDAMLGAIALGDIGQHFPPTDDRWKGADSSEFVRHCDGLLRERGWRVGNTDITVICERPKVGPHALAMRERIGELLQLPLDAVSVKATTSEKLGFTGRGEGIAAQAVVLLVAA
>NZ_CP040429|1645080:1705758|1652599_1654423_+|WP_154881322.1|terminase|DBSCAN-SWA
MVAGRIVAGPHVRNACRRHLQDLIQGPERGLFFDHEAADYAFRYFENVLMLSEGQFEGRKFELHPSQAFIIGSLFGWKGPDGLRRFRRAYIEQGKGNGKSPLAGGLGLLGMTAAGEAGAQIYAAAAKKDQAGILFADAVKMVKKSPLLAKRVEFAGGEGREFSMAHHASASFFRPVSRDTGRTGSGPRPYFVLVDEVHELPDRRIIEMLERGFKFRREPLLFMITNSGSDRTSVCWEEHEHAVKVAAGHTEAVNDPTFIGDVIDDRTFSYVCSLDDGDDPLEDPSCWAKANPLLGVTITEQYLADVVAQAKAIPGSLNGILRLHFCVWTDAETAWMTRPTLEPALADFDPHVHAGRKVYLGLDLSQVRDITAMAAVVETGTVPVEVEVEGEKLIIEKPTFDAWIEAWTPGDTLDARQLQDKLPYRAWVNGGFLHAPQGQAINFRHVAQVMAEYDNRYVVQLVAYDRYAFRRFEEEVNDIGLSVTFAEHPQGGCKKGKPLDAAVEAAEQSGQPAPEGMWMPGSLRLLEEALLEGRLRLRRNPVLVSAIMSAVIESDRWGNSWLSKARSANKIDAAVALCMAIGAAHAMPQDSGGIDDYLENGFFGLIG
>NZ_CP040429|1645080:1705758|1650877_1651156_+|WP_154879876.1|DBSCAN-SWA
MRVIVVVTAALLAACQAAPTKPNPPAPALIKVPVATYVPIDAALTKRCSWVRDGKPSAVFDVSNGRKRCLMQYEAQFEAIGQVQGKPVPEHE
>NZ_CP040429|1645080:1705758|1659234_1659591_+|WP_154879892.1|DBSCAN-SWA
MSYEPSLHALIAPLVQGRFYPDAPPDQQVFPFALYQQVGGQALWFLEGSMPDHKHARVQITVWAKSRPEANTLIRRMEDAICSGVPHSEPYGAAVAMYESPIKAYGARLDFGLWFPDP
>NZ_CP040429|1645080:1705758|1685306_1685741_-|WP_025878883.1|DBSCAN-SWA
MRRLLLPLLLSLAAVGCSSEPSGPPPGGTIATFERIDTQPGSGAEAVPGQKVSVHYTGWIYDERADNKHGKTFDSSVERGEPFTFTLGAGQVIRGWDEGVAGMKVGGKRTLMIPPEFGYGDRQVGPIPAGSSLVFDVELLNVQQ
>NZ_CP040429|1645080:1705758|1648846_1649389_+|WP_154879869.1|DBSCAN-SWA
MWKALRQLITPLAYLRISAEGWGKVMIDWLLPGLLAAGVTTIWWNWPSLVPLGGGSGLLVGVGAVMQILVGFYVAALAAIATFPTLSLENDVHRMTLDGGKIKRRKLLGYLFGYLAVLSMAMLVAMLFRNLPQEAVKLASPEVARWLKALGYFVYQFVLWQMISITLFGIHYLADRIHRS
>NZ_CP040429|1645080:1705758|1691886_1693008_+|WP_025878891.1|DBSCAN-SWA
MLTLVLVVILAALVFEFINGFHDTANSIATVVATKVLSPGWAVMLAAFMNLIGALTGTAVALTIASGLLNTNVVDVTPQVILCALLGGIIWNLITWWKGLPSSSSHALIGGLCGAGLAAAHNNWDALIWSERLGSWAQNKGLLWKVFVPMITSPIAGFLLGIAVMVLLWALIAGLAKIGGAIGRLARPRIVNAFFGKAQIASAAYMGFAHGHNDAQKTMGIIAMTLIGAEATGALNDLPSWLAFMHPDAHAGDGIAMWIVLTCAVVMAAGTASGGWKIIKTLGHKMVKLHPIHGFAAETSSATVLTLAAHFGMPVSTTHSISTAIMGVGFAKNPRSLRLGVIERIVWAWILTIPAAGGCAYLILKLFELLGWT
>NZ_CP040429|1645080:1705758|1695813_1697703_-|WP_025878894.1|DBSCAN-SWA
MNARYNAADIEVLSGLDPVKRRPGMYTDTARPNHLAQEVIDNSVDEALAGHARSIEITLFKDGSVEVSDDGRGMPVDIHPEEKIPGVELILTRLHAGGKFNNNNYTFSGGLHGVGVSVVNALSTLVEIHIKRDGAEHRITFRNGDRASPLEVVGTVGKKNTGTRLRFWPDPKYFDTPKFAVRALKHLLRAKAVLCPGLTVKLTDEATGEVDTWYYEDGLRDYLKLELGDRESLPADLFVGNLKKDTEIVDWAVAWLPEGELVQESYVNLIPTAQHGTHANGLRTGLTEALREFCDFRNLLPRGVKLAPEDVWDRVSFVLSLKMTDPQFSGQTKERLSSRQAAGFVEGAAHDAFSLLLNQNVELGEKIAQIAIERASARLKTEKLVVRKKVTQGPALPGKLADCISQDLSRTELFLVEGDSAGGSAKQARDKDFQAILPLRGKILNTWEVSSNSVLASEEVHNLAVAIGCDPGKEDISGLRYGKVIILADADSDGLHIATLLTALFLKHFPALVDAGHVFVAMPPLFRIDVGKQVFYALDEEEKRSMLDKIEREKIKGAINVTRFKGLGEMNPPQLRESTIHPDTRRLVQLTIDDGEQTHSLMDMLLAKKRASDRKGWLESKGDLASLEV
>NZ_CP040429|1645080:1705758|1681900_1683523_+|WP_025878880.1|DBSCAN-SWA
MHRYIVYLLAILMFPICLWLATIWPAWYWGVGITAAMVALGTWDLLQKRSTLRRNYPVMAHFRYGLESIGPEIRQYFVQSDLEDVPFSRQQRALIYQRAKNQMDTVPFGTLRSTYAVDYEWINHSLAPTTIAKHDFRVLIGPNCAKPYSASVFNISAMSFGSLSANAIRALNEGARLGGFYHDTGEGSISPYHREMGGDLVWEIGSGYFGCRDEKGGFSEERFVANANHDQVKMIEIKLSQGAKPGHGGVLPAPKVTAEISVTRGVPMGVDCVSPSRHSAFSTPVELLQFVARLRELSGGKPVGFKLAIGHPWEWFGIAKAMHETGLLPDFIVVDGAEGGTGAAPAEFVDHVGVPMHEALLLVHNTLVGLDLREHIRIGAAGKITSAFDIARTIAMGADWCNAGRGFMFALGCIQSLSCHTDKCPTGIATQDPARWKHLDAPDKATRVYSFHEHTLHALKELLCAAGLNDPAELGPEHILRRVSPVEIRSLASLYRYLEPGELLHKVPDHAVFHSFWADARSDSFQPPPKIQALRASKSR
>NZ_CP040429|1645080:1705758|1649941_1650397_+|WP_031270409.1|DBSCAN-SWA
MTEPVSTLKTIVGTFTAAVVAPATADALREAERVILGVPQSVLLVAMAGALIGVLLLPEKDAERVAADASRRRGHRLLQTAARWAALAVAVVAYAIVAAWVIAVAASIWPALAGAPQLPLAGLSGVLIRRLLPGYVRMVERATGAIGGDKP
>NZ_CP040429|1645080:1705758|1655671_1656316_+|WP_154879882.1|head,protease|DBSCAN-SWA
MLSKYSCPFEVKAADDAGNFEGYASVFNNVDLGEDLILPGAFVKVKTTRTGRLRLALYHNLTRLIGDAEFKQDDNGLHLKGKVNLNVSYAKDAYELMKAGTLDEMSVGFNTLEDAIENREGRRVRVIKKAELWEASVVPFGMNPEAQVMSVKSDVRAFESALRERMGLSQKEAAAVASLGFPAIHRDGGIGDTETVKQLQKLGNSIQSIFEGTN
>NZ_CP040429|1645080:1705758|1704726_1705758_+|WP_154879952.1|tRNA|DBSCAN-SWA
MIPLPLAFGAPLLQARIRTTPEDFQVDELPAFEATGEGEHLLLHIRKRGANTVHVAKVLAKWAGLPEMAVSYAGMKDRNAVTTQRFSVHLPKRVAPDLAELASDEIEVIDSTWHNRKLQRGALAGNRFRLVLRDVQGDAAAIDERLQQIAARGLPNWFGEQRFGRDGGNVPAALAMFGGRRMRKDQRSLLLSAARSALFNRVLAARVEQGSWDQPLQGEVWMLDGSRSVFGPEPYSDVLAERLARFDIHPSAPLWGEGELRSSDAARELELAALDDDESKALRTGLEEARLKQERRALRLRPALLQHQWLAADVLELSFALPPGCYATAVLHELGPVGDASQA
>NZ_CP040429|1645080:1705758|1658387_1658738_+|WP_154879888.1|head,tail|DBSCAN-SWA
MRAGLLNRKARVERPVSGTDSWGQPLQGWELVDEIMVGVAGETGLGAIRAGLLGGVPASISRYSFMARYQTVKALGIDATMRILYEGLVFEVKGIARDLKHKDRAFIITEEGGNSG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_154879863.1|1645080_1646517_+	AAA family ATPase	A0A2H4PAV8	Aphanizomenon_phage	2.2e-30	28.8
WP_154879865.1|1646727_1647273_+	hypothetical protein	NA	NA	NA	NA
WP_154879867.1|1647269_1647704_+	hypothetical protein	NA	NA	NA	NA
WP_154879869.1|1648846_1649389_+	hypothetical protein	A0A0R6PJ56	Moraxella_phage	9.7e-08	28.4
WP_154879871.1|1649456_1649945_+	glycoside hydrolase family protein	D5LH07	Escherichia_phage	5.8e-68	78.9
WP_031270409.1|1649941_1650397_+	hypothetical protein	K7ZPX3	Xanthomonas_citri_phage	1.7e-13	38.3
WP_154879874.1|1650393_1650876_+	hypothetical protein	NA	NA	NA	NA
WP_154879876.1|1650877_1651156_+	hypothetical protein	NA	NA	NA	NA
WP_154879878.1|1651155_1651518_+	DUF1064 domain-containing protein	Q3HQZ9	Burkholderia_phage	2.2e-40	65.3
WP_154881323.1|1652304_1652583_+	hypothetical protein	NA	NA	NA	NA
WP_154881322.1|1652599_1654423_+|terminase	terminase large subunit	A0A0U2C138	Paracoccus_phage	2.8e-160	50.1
WP_154879880.1|1654419_1655679_+|portal	phage portal protein	A0A2H4JFN7	uncultured_Caudovirales_phage	1.1e-163	71.6
WP_154879882.1|1655671_1656316_+|head,protease	HK97 family phage prohead protease	A0A2H4JA51	uncultured_Caudovirales_phage	9.2e-82	73.5
WP_154879885.1|1656315_1657527_+|capsid	phage major capsid protein	A0A2H4J8D1	uncultured_Caudovirales_phage	1.3e-140	64.3
WP_154879887.1|1658079_1658388_+|head,tail	phage gp6-like head-tail connector protein	A0A2H4J8C5	uncultured_Caudovirales_phage	3.2e-24	57.1
WP_154879888.1|1658387_1658738_+|head,tail	head-tail adaptor protein	NA	NA	NA	NA
WP_154879890.1|1658734_1659238_+	HK97 gp10 family phage protein	Q2NPI1	Xanthomonas_virus	8.7e-27	39.7
WP_154879892.1|1659234_1659591_+	DUF3168 domain-containing protein	NA	NA	NA	NA
WP_154879894.1|1659661_1660321_+|tail	phage tail protein	C4ML12	Xanthomonas_virus	4.4e-63	57.7
WP_154879896.1|1660320_1660629_+	hypothetical protein	NA	NA	NA	NA
WP_154879898.1|1660637_1660937_+	hypothetical protein	NA	NA	NA	NA
WP_154879900.1|1661434_1664224_+|tail	phage tail tape measure protein	A0A1V0E821	Vibrio_phage	1.6e-85	29.9
WP_154879902.1|1664220_1664550_+|tail	phage tail protein	A0A2R3UA73	Siphoviridae_environmental_samples	1.2e-24	52.7
WP_154879904.1|1664559_1665672_+	hypothetical protein	Q2PGC3	Xanthomonas_phage	5.8e-39	39.1
WP_154879906.1|1665674_1666148_+	hypothetical protein	NA	NA	NA	NA
WP_154879908.1|1666144_1666837_+|tail	phage minor tail protein L	A0A2R3UA90	Siphoviridae_environmental_samples	7.4e-85	61.5
WP_154879910.1|1666929_1667670_+	peptidase P60	A0A2R3UAR4	Siphoviridae_environmental_samples	1.5e-83	60.3
WP_154879912.1|1667662_1668280_+|tail	tail assembly protein	Q6JIL3	Burkholderia_virus	2.9e-48	56.1
WP_154879914.1|1668276_1671807_+	DUF1983 domain-containing protein	A0A2R3UA88	Siphoviridae_environmental_samples	0.0e+00	61.7
WP_154879916.1|1671806_1672196_+	hypothetical protein	NA	NA	NA	NA
WP_154879918.1|1672195_1672933_+	hypothetical protein	NA	NA	NA	NA
WP_154881324.1|1672983_1673916_+	hypothetical protein	NA	NA	NA	NA
WP_154879920.1|1673912_1674188_-	hypothetical protein	NA	NA	NA	NA
WP_154879922.1|1674249_1674864_+	hypothetical protein	NA	NA	NA	NA
1674636:1674651	attL	NA	NA	NA	NA
WP_154879924.1|1675326_1675821_+	hypothetical protein	B7SYF7	Stenotrophomonas_phage	3.6e-41	54.4
WP_154879927.1|1675970_1677533_-	hypothetical protein	R9TRQ8	Vibrio_phage	7.6e-29	28.9
WP_154879929.1|1677586_1678561_-|integrase	tyrosine-type recombinase/integrase	A0A1B1P9F9	Acinetobacter_phage	1.3e-71	44.8
WP_080278357.1|1678924_1679947_+	TraB/GumN family protein	NA	NA	NA	NA
WP_080149520.1|1680011_1680458_+	BLUF domain-containing protein	NA	NA	NA	NA
WP_154879932.1|1680569_1681856_+	nucleotide sugar dehydrogenase	NA	NA	NA	NA
WP_025878880.1|1681900_1683523_+	FMN-binding glutamate synthase family protein	NA	NA	NA	NA
WP_025878881.1|1683585_1684047_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_154879936.1|1684072_1685320_-	TIGR03862 family flavoprotein	NA	NA	NA	NA
WP_025878883.1|1685306_1685741_-	peptidylprolyl isomerase	NA	NA	NA	NA
WP_032976499.1|1685810_1686176_+	membrane protein	NA	NA	NA	NA
WP_032976500.1|1686472_1687240_+	sulfurtransferase	NA	NA	NA	NA
WP_154879939.1|1687362_1688358_+	MsnO8 family LLM class oxidoreductase	NA	NA	NA	NA
WP_154879941.1|1688425_1688923_+	general stress protein	NA	NA	NA	NA
WP_025878888.1|1689012_1689666_-	exopolysaccharide biosynthesis protein	NA	NA	NA	NA
WP_049464874.1|1689649_1690969_-	HlyC/CorC family transporter	NA	NA	NA	NA
WP_025878890.1|1691246_1691873_+	DUF47 family protein	NA	NA	NA	NA
WP_025878891.1|1691886_1693008_+	inorganic phosphate transporter	NA	NA	NA	NA
WP_154879944.1|1693483_1694980_-	peptidase S10	NA	NA	NA	NA
WP_059063745.1|1695078_1695657_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_025878894.1|1695813_1697703_-	DNA topoisomerase IV subunit B	G3M9Z3	Bacillus_virus	8.1e-94	34.7
WP_154879947.1|1697863_1698097_+	hypothetical protein	NA	NA	NA	NA
WP_025878896.1|1698498_1700163_+	CTP synthase	A0A1J0FA14	Only_Syngen_Nebraska_virus	4.6e-141	50.9
WP_012510652.1|1700251_1701082_+	3-deoxy-8-phosphooctulonate synthase	E3T537	Cafeteria_roenbergensis_virus	7.5e-52	42.3
WP_154879949.1|1701078_1701426_+	hypothetical protein	NA	NA	NA	NA
WP_105163832.1|1701425_1701758_+	hypothetical protein	NA	NA	NA	NA
WP_032976506.1|1701855_1703148_+	phosphopyruvate hydratase	A0A1X9I5Z8	Streptococcus_phage	1.4e-142	61.9
WP_025878900.1|1703152_1703503_+	cell division protein FtsB	NA	NA	NA	NA
WP_032976507.1|1703499_1704198_+	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase	NA	NA	NA	NA
WP_025878902.1|1704232_1704730_+	2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase	NA	NA	NA	NA
WP_154879952.1|1704726_1705758_+|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
1708695:1708710	attR	NA	NA	NA	NA