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_CP009285	Paenibacillus borealis strain DSM 13188 chromosome, complete genome	22 crisprs	PrimPol,WYL,csa3,DEDDh,cas3,cas5,cas8c,cas7,cas4,cas1,cas2,cas14j,DinG	1	14	8	0

1. NZ_CP009285

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP009285_1

• CRISPR_ID: NZ_CP009285_1
• CRISPR_location: 514249-514383
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_1

Consensus_repeat	Method
GTTAGTTTTGTACGAAGCAGATTCAGGATGCCTAAGCTAACAAAACTT	CRISPRCasFinder

spacers of NZ_CP009285_1

>1.1|514297|39|NZ_CP009285|CRISPRCasFinder
AAGCGAATGCTCCATAAAACTTAAGCGAATGCTTCCGTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_1

CRISPR arrays

The CRISPR arrays of NZ_CP009285_1

>merge|NZ_CP009285|1|514249-514383|CRISPRCasFinder
GTTAGTTTTGTACGAAGCAGATTCAGGATGCCTAAGCTAACAAAACTTAAGCGAATGCTCCATAAAACTTAAGCGAATGCTTCCGTTGTTAGTTTTGTACGAAGCAGATTCAGGATGCCTAAGCTAACAAAACTT

>NZ_CP009285|1|1|514249-514383|CRISPRCasFinder
GTTAGTTTTGTACGAAGCAGATTCAGGATGCCTAAGCTAACAAAACTT	AAGCGAATGCTCCATAAAACTTAAGCGAATGCTTCCGTT
GTTAGTTTTGTACGAAGCAGATTCAGGATGCCTAAGCTAACAAAACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_039299580.1|515364_515586_+|YezD-family-protein	unknown	unknown	gnl|CDD|378371
NZ_CP009285.1|WP_042210229.1|505320_506283_-|L-lactate-dehydrogenase	unknown	unknown	gnl|CDD|133427
NZ_CP009285.1|WP_042210233.1|513320_514172_+|sulfate-ABC-transporter-permease-subunit-CysT	unknown	unknown	gnl|CDD|131194
NZ_CP009285.1|WP_036732764.1|507344_507605_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl|CDD|225170
NZ_CP009285.1|WP_081971881.1|498883_499978_-|cation-transporter	unknown	unknown	gnl|CDD|224151
NZ_CP009285.1|WP_052429294.1|509288_511622_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|372282
NZ_CP009285.1|WP_042210232.1|512083_513205_+|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224529
NZ_CP009285.1|WP_042210241.1|521049_521466_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|235142
NZ_CP009285.1|WP_042210231.1|507857_508907_+|lactonase-family-protein	unknown	unknown	gnl|CDD|378416
NZ_CP009285.1|WP_042210238.1|517577_519452_+|bifunctional-ADP-dependent-NAD(P)H-hydrate-dehydratase/NAD(P)H-hydrate-epimerase	unknown	unknown	gnl|CDD|182554
NZ_CP009285.1|WP_042210228.1|503212_505213_+|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_CP009285.1|WP_042210240.1|520009_520906_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235853
NZ_CP009285.1|WP_042210227.1|500636_502961_+|cadmium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319847
NZ_CP009285.1|WP_042210230.1|506640_507147_-|cytochrome-c-biogenesis-protein-CcdC	unknown	unknown	gnl|CDD|377808
NZ_CP009285.1|WP_042210237.1|516766_517399_+|NAD(P)H-binding-protein	unknown	unknown	gnl|CDD|225462
NZ_CP009285.1|WP_042210239.1|519485_519941_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210234.1|514398_515262_+|sulfate-ABC-transporter-permease-subunit-CysW	unknown	unknown	gnl|CDD|226665
NZ_CP009285.1|WP_042210242.1|521587_522298_+|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta	unknown	unknown	gnl|CDD|129802
NZ_CP009285.1|WP_042210235.1|515715_516024_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210236.1|516298_516715_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_039299580.1|515364_515586_+|YezD-family-protein	gnl|CDD|378371	pfam10055, DUF2292, Uncharacterized small protein (DUF2292). Members of this family of hypothetical bacterial proteins have no known function.	1.77032e-14
NZ_CP009285.1|WP_042210229.1|505320_506283_-|L-lactate-dehydrogenase	gnl|CDD|133427	cd05291, HicDH_like, L-2-hydroxyisocapronate dehydrogenases and some bacterial L-lactate dehydrogenases. L-2-hydroxyisocapronate dehydrogenase (HicDH) catalyzes the conversion of a variety of 2-oxo carboxylic acids with medium-sized aliphatic or aromatic side chains. This subfamily is composed of HicDHs and some bacterial L-lactate dehydrogenases (LDH). LDHs catalyze the last step of glycolysis in which pyruvate is converted to L-lactate. Bacterial LDHs can be non-allosteric or may be activated by an allosteric effector such as fructose-1,6-bisphosphate. Members of this subfamily with known structures such as the HicDH of Lactobacillus confusus, the non-allosteric LDH of Lactobacillus pentosus, and the allosteric LDH of Bacillus stearothermophilus, show that they exist as homotetramers. The HicDH-like subfamily is part of the NAD(P)-binding Rossmann fold superfamily, which includes a wide variety of protein families including the NAD(P)-binding domains of alcohol dehydrogenases, tyrosine-dependent oxidoreductases, glyceraldehyde-3-phosphate dehydrogenases, formate/glycerate dehydrogenases, siroheme synthases, 6-phosphogluconate dehydrogenases, aminoacid dehydrogenases, repressor rex, and NAD-binding potassium channel domains, among others.	1.17729e-166
NZ_CP009285.1|WP_042210233.1|513320_514172_+|sulfate-ABC-transporter-permease-subunit-CysT	gnl|CDD|131194	TIGR02139, permease_CysT, sulfate ABC transporter, permease protein CysT. This model represents CysT, one of two homologous, tandem permeases in the sulfate ABC transporter system; the other is CysW (TIGR02140). The sulfate transporter has been described in E. coli as transporting sulfate, thiosulfate, selenate, and selenite. Sulfate transporters may also transport molybdate ion if a specific molybdate transporter is not present. [Transport and binding proteins, Anions].	2.90851e-137
NZ_CP009285.1|WP_036732764.1|507344_507605_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl|CDD|225170	COG2261, COG2261, Predicted membrane protein [Function unknown].	2.59603e-11
NZ_CP009285.1|WP_081971881.1|498883_499978_-|cation-transporter	gnl|CDD|224151	COG1230, CzcD, Co/Zn/Cd efflux system component [Inorganic ion transport and metabolism].	1.47591e-103
NZ_CP009285.1|WP_052429294.1|509288_511622_-|alpha/beta-hydrolase	gnl|CDD|372282	pfam12740, Chlorophyllase2, Chlorophyllase enzyme. This family consists of several chlorophyllase and chlorophyllase-2 (EC:3.1.1.14) enzymes. Chlorophyllase (Chlase) is the first enzyme involved in chlorophyll (Chl) degradation and catalyzes the hydrolysis of an ester bond to yield chlorophyllide and phytol. The family includes both plant and Amphioxus members.	1.1472e-05
NZ_CP009285.1|WP_042210232.1|512083_513205_+|sulfate-ABC-transporter-substrate-binding-protein	gnl|CDD|224529	COG1613, Sbp, ABC-type sulfate transport system, periplasmic component [Inorganic ion transport and metabolism].	0
NZ_CP009285.1|WP_042210241.1|521049_521466_+|GNAT-family-N-acetyltransferase	gnl|CDD|235142	PRK03624, PRK03624, putative acetyltransferase; Provisional.	1.3471e-19
NZ_CP009285.1|WP_042210231.1|507857_508907_+|lactonase-family-protein	gnl|CDD|378416	pfam10282, Lactonase, Lactonase, 7-bladed beta-propeller. This entry contains bacterial 6-phosphogluconolactonases (6PGL)YbhE-type (EC:3.1.1.31) which hydrolyze 6-phosphogluconolactone to 6-phosphogluconate. The entry also contains the fungal muconate lactonising enzyme carboxy-cis,cis-muconate cyclase (EC:5.5.1.5) and muconate cycloisomerase (EC:5.5.1.1), which convert cis,cis-muconates to muconolactones and vice versa as part of the microbial beta-ketoadipate pathway. Structures of proteins in this family have revealed a 7-bladed beta-propeller fold.	1.94469e-139
NZ_CP009285.1|WP_042210238.1|517577_519452_+|bifunctional-ADP-dependent-NAD(P)H-hydrate-dehydratase/NAD(P)H-hydrate-epimerase	gnl|CDD|182554	PRK10565, PRK10565, putative carbohydrate kinase; Provisional.	1.68315e-78
NZ_CP009285.1|WP_042210228.1|503212_505213_+|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.13523e-58
NZ_CP009285.1|WP_042210240.1|520009_520906_-|SDR-family-oxidoreductase	gnl|CDD|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	2.45595e-158
NZ_CP009285.1|WP_042210227.1|500636_502961_+|cadmium-translocating-P-type-ATPase	gnl|CDD|319847	cd07548, P-type_ATPase-Cd_Zn_Co_like, P-type heavy metal-transporting ATPase, similar to Bacillus subtilis CadA which appears to transport cadmium, zinc and cobalt but not copper out of the cell. Bacillus subtilis CadA/YvgW appears to transport cadmium, zinc and cobalt but not copper, out of the cell. Functions in metal ion resistance and cellular metal ion homeostasis. CadA/YvgW is also important for sporulation in B. subtilis, the significant specific expression of the cadA/yvgW gene during the late stage of sporulation, is controlled by forespore-specific sigma factor, sigma G, and mother cell-specific sigma factor, sigma E. This subfamily also includes Helicobacter pylori CadA an essential resistance pump with ion specificity towards Cd(2+), Zn(2+) and Co(2+), and Zn-transporting ATPase, ZiaA(N) in Synechocystis PCC 6803. Transcription of ziaA is induced by Zn under the control of the Zn responsive repressor ZiaR. This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP009285.1|WP_042210230.1|506640_507147_-|cytochrome-c-biogenesis-protein-CcdC	gnl|CDD|377808	pfam07301, DUF1453, Protein of unknown function (DUF1453). This family consists of several hypothetical bacterial proteins of around 150 residues in length. The function of this family is unknown. Members of this family seem to be found exclusively in the Order Bacillales.	6.76218e-59
NZ_CP009285.1|WP_042210237.1|516766_517399_+|NAD(P)H-binding-protein	gnl|CDD|225462	COG2910, COG2910, Putative NADH-flavin reductase [General function prediction only].	1.12849e-70
NZ_CP009285.1|WP_042210234.1|514398_515262_+|sulfate-ABC-transporter-permease-subunit-CysW	gnl|CDD|226665	COG4208, CysW, ABC-type sulfate transport system, permease component [Inorganic ion transport and metabolism].	3.3394e-150
NZ_CP009285.1|WP_042210242.1|521587_522298_+|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta	gnl|CDD|129802	TIGR00719, Probable_L-serine_dehydratase_beta_chain, L-serine dehydratase, iron-sulfur-dependent, beta subunit. This enzyme is also called serine deaminase. This model describes the beta chain of an iron-sulfur-dependent L-serine dehydratase, as in Bacillus subtilis. A fairly deep split in a UPGMA tree separates members of this family of beta chains from the homologous region of single chain forms such as found in E. coli. This family of enzymes is not homologous to the pyridoxal phosphate-dependent threonine deaminases and eukaryotic serine deaminases. [Energy metabolism, Amino acids and amines, Energy metabolism, Glycolysis/gluconeogenesis].	6.43445e-64
NZ_CP009285.1|WP_042210236.1|516298_516715_+|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.02583e-09

Protein sequences

>NZ_CP009285.1|WP_042210233.1|513320_514172_+|sulfate-ABC-transporter-permease-subunit-CysT
MNVTTNAAAAAVSRRRLLPGFGITMGFSVLYLSLVVLLPLSALLFNSTGLSWAKFWDVATDARVLASYRVSLSTAAAAALIDAVLGLLLAWVLVRYEFPGKRLFDALIDLPFALPTAVAGVSLTALYSQNGWIGSLLEPLGLRVAFTPLGITLALMFIGIPFVVRTVQPVLEDLDRDMEEASATLGAGRWRTFVRIVMPELFPPLLTGFALAFARGIGEYGSVVFISGNMPMRTEIAPLLIMSKLEQFDYAGATAVALLLLLISFLMLLVINSLQHWARKSSR
>NZ_CP009285.1|WP_042210232.1|512083_513205_+|sulfate-ABC-transporter-substrate-binding-protein
MKKGIKKGLIAGFTLLLTAGLTACGNNNAGNSAGAATEAPAATEAAANTAATPEATKAPAKDPVELLNVSYDPTRELYENYNKAFAAYWEQETGQKVTIKQSHGGSGKQSRAVLDGLEADVVTLALGYDIDALQETGLIGADWQSKYEHNSSPYTSTIVFLVRKGNPKGIKDWPDLLKDDVEVITPNPKTSGGARWNYLAAWGYALDQNNNDEAKAQEFVQKLFKNVPVLDTGARGSTTTFVERGIGDVLIAWENEAYLSIKELGPDKFEIVNPSESILAEPPVAVVDKIVDKRGTREVADAYLKYLYTEEGQKIAAENYYRPTLESVKEQFKDQFPEIKLFTLADKFGTWKETQEKHFNDGGIFDKIYVPGS
>NZ_CP009285.1|WP_052429294.1|509288_511622_-|alpha/beta-hydrolase
MGMDLEYAPAPQGPRLHRRILRELGRRILETYRYDTTLWRIALCGPWILCILAFTIAVMGIPTGLGSAADIILAAGAGTLVMALAGNLLAVLLSLTGLRIPHLFTGSLLSALSAVLLILYYADLELEAAAVIAGIAALASGLGGLAAGMLRTRRSLTGGLLAAVLVLTPLALAYGTGSSSPAPYPSLQTLAADGEVLPAAAADPSQPGDYTFHSFTYGSGQDLQRKEYGADAALLSASVDATEYITSWPTLRTLFWGFDPGALPLNARVWMPDGDGPYPLVLMVHGNHMMEDYSEGGYAYLGELLASRGFIAVSLDENFLNYSAWSGIPDNDFKVRTWMILKHLQQIAGFAEQSGTPFYQKVDYDRTALLGHSRGGQAVAMAADASRWFTGDPALAAVKQFNITSVIALAPTDKVIDSKQASLVDVNYLTLQGARDGDVHDFYGDRQYMRSSYSGSTSAFKSSLYIAGANHSQFNTDWGLFDQTMPTGLFLKRTDIMDGDEQRQIAKVYVSAFLETTLHGKPEYQQLFRDYRSGAQWLPDTAYYNRFQSGTYITVANYEEDRKRNTVKGGTATAEGLTWSEEAAKDRESKNKPSYGILLERSSTPQNQDEDAAADSVEASYSIKLNEALTRKLANSAAEGLAFSLANRNSDADDDEDAAAPSEAALSPDVEVELTDSNEVTARLPLDEVMEILPLPQTEFTISPWLEERISDGKFGDLSEAVFQTYELPFELFLEEEPALDPDKLTEITFYLQGEDDKIMLDDIGFYERDDQLQGLQ
>NZ_CP009285.1|WP_042210231.1|507857_508907_+|lactonase-family-protein
MHQPNEVLFYIGTYSSEKEEAILLGALNKETGEMRVMGGTRGIENPSYLAVNAAGTVLYAVSEQDEGRVYAYAIEPGSKALRLLGSRPTGGGAPCYVSVAPQEDYIFVSNYTGGNVNVFPLNPDGSLQDMSSQVKHEGSGIRADRQDAPHPHSVIPDKTGEHVLVCDLGLDQIVFYRVEEGKLVTHREVDLPPGSGPRHLAIHPSRQWIYLVNELNNTVTVFADDEQQGNLKILQNVSSLPEHYTAGSDDTAADIHVSPCGRYLYVSNRGHDSIALFHIDNATGLLEAEDWVISGGRTPRNFAIISGMLLAANQNSGNIVSFRIDSESGRLIPTGNELEIPSPVCIVSV
>NZ_CP009285.1|WP_036732764.1|507344_507605_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MSLLWMLIVGGVIGWLAGLIMGRDIPGGIIGNIIAGILGSWLGGMLLGSWGPKISDYYVFPSLIGAVVLIFIVSLILRSVGGRSRS
>NZ_CP009285.1|WP_042210230.1|506640_507147_-|cytochrome-c-biogenesis-protein-CcdC
MGNINPSLLHVGSTLGAVFMALMVIFIRLKASARPVTIRKIWIPPLGMSTGFAMFVVPEVRFPWWWAVAAFLVGWFIFAYPLMRSTRFEEREGQIYAQRSKSFAFILLGLLLIRTLLHEFINQYVSVPQSGGLFFILAFGMILHWRVFMYKHYTQMLPAEAQIPQPRG
>NZ_CP009285.1|WP_042210229.1|505320_506283_-|L-lactate-dehydrogenase
MKSKSRKVAIVGSGMVGSSCAYSMVNQAICDEIMMIDRTYDRAMAQALDLSHCMDFTGTRTKVYAGTSSDCAGMDVVILTAGANPKPGQTRLDVLDAAAVITKEIVTEIMAGGFDGIFVVAANPVDIVTYMVWKISGLPRHRIIGTGTSIDSSRLKTLLSEVFTIDPRSVNGYALGEHGESQFVAWSHVTIGGKPILQIMEQHRERFSTLDLEDIARKTKDAGWEIFTRKGSTHFGIGSALAYITRSILNDEHKIIAVSAILDGEYGQSGVCAGAPAIISSSGIQELLELNLSDAEMAKFEASCSIIRGGIDSLQLEQKL
>NZ_CP009285.1|WP_042210228.1|503212_505213_+|methyl-accepting-chemotaxis-protein
MKMNANNGKSGSLQKKWSLVILAVAIVPLLGATLFFMQYFGGVTRADSEELAESILEMNTTRIDEWINAKTSAVQELMAMHPEFDTSKPGTIFPVIKVLEDSDRQSEGYSVINKEGILSNSLNLTADVSGEAYFQEAKTSHAPAVADMSFLEQLNKNIIPVFVPAVDKDNQFAGGIAFSVTPDILTEMSKNIHVAETGYGYVISAQGNYYTSSDMDRIGKNIADYAGTPGMKEAIKNILANEQGSETYKDEDGKQVITYFRTIPSTDWKLLISVPKSEITAKVTSAQTISLLFIIVVILVVIAISLYLTRLIVKPIVAISGVMRRVAEGHLSERVAVRSGDEIGQMSQSINDMIGGLAGIVGKIDATVAQVAVSGEGVLNYANQTSNTSAEIETVVQEVARGMEEQFRGSEQAARATEEMAIGLQRIAESSVSVSDQAETVSSEVESGYLEIQATLEQMTVISTTAGQTAELISNLTGQSEQIGQIIDVISEISNQTGLLSLNASIEAARAGEHGRGFGVVANEVKKLAERTNGAIVNIVELIRQIQDSTRDAAVSMEKSIVEIGDGMGKMKNVGESFNHIRSSIREVSLQIQDVSAINEQMSAGTEEITASISDMLIIARESAESAEMVAEASTEQRSLMGRVVTSAESLNGLMSELRSEIEKFH
>NZ_CP009285.1|WP_042210227.1|500636_502961_+|cadmium-translocating-P-type-ATPase
MNTVQGNVKRKWVLEGLDCANCAMKIENKVKKIEGVSSCSVNFATKTMTLETAASAAEEVAEQAQHTVTKLEPHVQLREVTASRAVKKPLAAGSPGQVRRVAVQGQEHNHTDGEPHSHEHDQDDAHGHTHAAAEHTHSHTSAAEHGHDHSHGHSHEHGEGNTRRIVLRLAGGAILAAAGMFLPVSGIAELLIFLAAYLIVGGEVVLSAVRNIIRGQVFDENFLMALATIGAFAIGEYPEGVAVMLFYQVGELFQGMAVNRSRRSITALMDIRPEFAYLKEGSNLRKVSPEEVAVGDSIVVKPGEKVPLDGIILEGSAMMDTSALTGESVPRSTQPGSQVLSGFINRNGVVTIEVTKDFGESAVSQILELVQNATNNKAKTENFITKFARAYTPVVVITALLLAVVPPLVLSGATFSDWIYRALVFLVISCPCALVVSIPLGFFGGIGAASRNGILVKGSNFLEALNDVKVVVFDKTGTLTKGQFSVTGNYPAEGFTQQELLRIAAYAESHSSHPIAESIRSAYGEAIPGEAITGYNEISGHGIAVTVEGKAVLAGNARLMEREGIASRTPQQSGTVVHIAVDKQYAGYIVIADEVKEDAQRAIQELNALGIRKTVMLTGDASSVAESVGRQLGIQEIHAELLPGDKVEAIERLEREKGPKEKIIFVGDGINDTPVLARADVGIAMGGLGSDAAIEAADIVIMTDEPSKIAAAIGIAKRTRTIVWQNIIFALGVKAVFLLLGAFGIATMWEAVFSDVGVTVLAVLNSMRALQPPK
>NZ_CP009285.1|WP_081971881.1|498883_499978_-|cation-transporter
MNNPKYPGSVTHDESQEHNHSEYSSHSDHSDHSEQHKHDTDRTVSSAGGHGHSGHQHSGHGAADHSHSHSHSHSHAPDNKKGLLIALIITGGIMFLEFFGGLVTGSLALLSDSGHMLSDTASLALSLVAMIIAVKPPSAKNSYGFYRFEIMAALFNGVTLFVIAGFIMWEAYQRFFSPPAVASGTMMLIAAVGLLANLISAWSLMRKSEAKDNINIRSAYLHIMGDALGSVGALLAGLIMNLFSWYVADPIISVLVALLILRSAWGVIKQAFHILMEGTPLTVNTRHVQEALLEIEGVLDVHDLHIWTITSGLDALSGHLLIGDHTDHQLVLQQAIKVVEEKFGIHHTTLQIENSSLKHGKLPV
>NZ_CP009285.1|WP_042210234.1|514398_515262_+|sulfate-ABC-transporter-permease-subunit-CysW
MAGTVPLHVPAPRKSVSSPRTTESKAVKWVLISLAGLVLLWLIALPLIIVLVESLKRGLDVYWAALTDPDAASALKLTLLVAAITVPLNTIFGVTAAWAVTKFRFRGKGFLITLIDLPFAVSPVIGGLIFILVFGSHGWFGPWLSNHDIKIVFALPGIVLATLFITFPFVARELIPLMDEQGTQEEEAAITLGAHGWQIFWRVTLPNIKWGLLYGIILCNARAMGEFGAVSVVSGHIRGETNTLPLHVEILYNEYQFSASFAVASLLLLLALVTMIVKSLLLRKNAH
>NZ_CP009285.1|WP_039299580.1|515364_515586_+|YezD-family-protein
MAKPLKVDEVWLARITELLDDMEFGSLHIVVHEGQIVQMERTERKRFENSTANARYSGETGSRRTDSRSAGRG
>NZ_CP009285.1|WP_042210235.1|515715_516024_-|hypothetical-protein
MSPIGKLFKWGTFAYEAFLALPFIGGAFVVANAWVPLGVAFLLHAVAVIILLRERGPIIGNAVGIVTSVVGLIPFVGWIMHAITAVILLVEGITGSRRNTRY
>NZ_CP009285.1|WP_042210236.1|516298_516715_+|GNAT-family-N-acetyltransferase
MDKTLQPDIRHELPSVEQYLALRLESGLSPMSVEGAGIGLPRSVFAVTLYEGDLLIGMGRVIGDGGCFFQVTDIAVKPAFQGRGLGKIIMREIRRFLETVPDKAYISLIADGEASRLYAQYGFAPVMPDSQGMFLRRS
>NZ_CP009285.1|WP_042210237.1|516766_517399_+|NAD(P)H-binding-protein
MDIVVFGASGKIGSAIVEEALKRKHEVTAAVRKPEAFSIQHDRLKAVAADLLDPASVADAVRGHEEVISAFGPAPGHENDLLQVADSLLTGMRAAGLQRLIVIGGAGSLKTESGEWLMDTADFPEDYRPLATAHANAYEIYRGSELDYTYLSPPAAIIAGRRTGQFRIGLDRLIVDENGRSSISIQDFAVAVIDELEEGNFSKARFTVGY
>NZ_CP009285.1|WP_042210238.1|517577_519452_+|bifunctional-ADP-dependent-NAD(P)H-hydrate-dehydratase/NAD(P)H-hydrate-epimerase
MDVVTAEEMRALDRETIERLGIPAIALMENAGRAIAEEVIALCRRRGAGDAGYGAGGGSADGGTRSYGAGAAGSADGGTRSYGVGAAGGAGGGLRSYKAGAAGGVAGGSGDGGTSSYGAGVAGGLESADAEGRGLGAWAAGGGPAIQPRGFSVSADSALTLAAAGAEHWLVLAGKGNNGGDGLAAARHLREAGIAVTLVYAAAPESLAGEAALQRDAAAAMGIPAVVYGRDAVDLAACSGIIDALLGTGSAGAPRGAYAELIAAANASGNPIVSADIPSGLDADTGETHEPCIHAAVTVCLAFLKRGLLQYPGAGAAGHVVVRSIGIPAALARESGVRVSLLTPEVLRTRLQVDVSRRRSPEGHKGTYGHVLLAAGSLRMSGAGLLSARAALRAGCGLVTWALPDKLLPYVIGCAPELMLAPVAGSDGEWHAGTAAEVLRLSGSRDCVAIGPGLGRFEGDTEWLRRLWEETDSPLVIDADALNILADADYSAWSRRHPVILTPHPGEMARLAGISTAGVQRDRIGLALSYAAAHGVILVLKGAHTVIATPEGQAYVNITGHPGMGTGGAGDVLTGIISGLLAQGLDAAQAAAFGVYLHGLAGEHAARKRDNPAALIAGDIIEAL
>NZ_CP009285.1|WP_042210239.1|519485_519941_-|hypothetical-protein
MTTHKDYDLPSVRLTAGMYALTKLSAAGLTFILVSLFMLGHGYEGGIPDGWPVSVPYAIYAYGLPAAILADALLRMFRSTTLSPALVLYAVAGYGAGLWLASEQGGDALTCGLTGLVVLLLFRLAQIAGERYPLLLPVFALFIPLLCLVLF
>NZ_CP009285.1|WP_042210240.1|520009_520906_-|SDR-family-oxidoreductase
MNPVYPYYGEKTVCRVQPIAFPPQHQDRQPGLESLMNPRPISENPDSSGGRLKGKVALITGGDSGIGRATAIAFAKEGADIAIVYLDEASDAAATQHRIEELGRRCLRIETDLRHKECCFEAVEHTVHTLGKLDILVNNHGVQYPQKSILDISEEQLYQTYRTNIFPFFFLTQAALPHLHKGSCIINTASITAYQGNKELIDYSSTKGAVVSFTRSLALSLADSGIRVNSVAPGPVWTPLIPSSYSAEKVSVFGTDTPFKRAAQPYELAGAYVYLASPDASYVTGTCIHVNGGDMVTS
>NZ_CP009285.1|WP_042210241.1|521049_521466_+|GNAT-family-N-acetyltransferase
MLYRPMTADDYEAAYHLWENTDGMGLSEADSRGEIVRYLERNPGISQVCVNEDGTLAGTAMCGHDGRRGYMYHVAVSSDSRGSGAGREMVTRCLERLREEGIMKCHLMVIGHNSLGRSFWTGTGWQERDGLVLFSRNS
>NZ_CP009285.1|WP_042210242.1|521587_522298_+|L-serine-ammonia-lyase,-iron-sulfur-dependent,-subunit-beta
MRFKDVFSIIGPAMVGPSSSHTAGAARIGRAARQVLGELPREAEITFFGSFAATYQGHGTDRAIAGGLLDFTTDDHRLPDSIELAAEAGMKISFGQGTGLFPHPNTVRLRLTGSESGIELTLTGISIGGGNIEIVDIDGFGVKLTGMYPTVLINHMDYLGVLASVTDVMRQGQCNIGHMSLDRKNRSGAALTVLELDEAATPELLLNLRALPAVKSVKVVDLNEQVQEQKGKDTTS

Crispr_ID: NZ_CP009285_2

• CRISPR_ID: NZ_CP009285_2
• CRISPR_location: 1503533-1504173
• CRISPR_type: TypeI
• Repeat_type: NA
• Spacer_info: 9 spacers
• Cas_protein_info: cas3,cas5,cas8c,cas7,cas4,cas1,cas2

Consensus repeat of NZ_CP009285_2

Consensus_repeat	Method
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	PILER-CR
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	CRT
CACTCCGTGTGGAGTGTGTGGATTG	CRISPRCasFinder

spacers of NZ_CP009285_2

>2.1|1503566|34|NZ_CP009285|PILER-CR,CRT
GTTTCAGCAGGTATATCCAATGACGATTCAGCAG
>2.2|1503633|36|NZ_CP009285|PILER-CR,CRT
GACACCACGGAGTAAGAGCCACTACATGTCTGGGAA
>2.3|1503702|34|NZ_CP009285|PILER-CR,CRT
ACACAGAAGCAGATTGATGCGGGTTGGGCGGATC
>2.4|1503769|34|NZ_CP009285|PILER-CR,CRT
ACTGATGAAATAACCAAGAAATATGAATTCCTGC
>2.5|1503836|35|NZ_CP009285|PILER-CR,CRT
TGCATAACGCTGAGATTCTTCGTTACGCCGACGGC
>2.6|1503904|33|NZ_CP009285|PILER-CR,CRT
TGCGTATGTACCACGACCCGTGCGTCCAGTTCG
>2.7|1503970|35|NZ_CP009285|PILER-CR,CRT
AGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCG
>2.8|1504038|35|NZ_CP009285|PILER-CR,CRT
GATTCAAATGGCAGGAATTTGCATGGCAGGCTTTG
>2.9|1504106|35|NZ_CP009285|CRT
TTGGATGCTTCGAGCTCAGTAAGAGCCTTGCGCTT
>2.10|1503562|42|NZ_CP009285|CRISPRCasFinder
AAATGTTTCAGCAGGTATATCCAATGACGATTCAGCAGGTCG
>2.11|1503629|44|NZ_CP009285|CRISPRCasFinder
AAATGACACCACGGAGTAAGAGCCACTACATGTCTGGGAAGTCG
>2.12|1503698|42|NZ_CP009285|CRISPRCasFinder
AAATACACAGAAGCAGATTGATGCGGGTTGGGCGGATCGTCG
>2.13|1503765|42|NZ_CP009285|CRISPRCasFinder
AAATACTGATGAAATAACCAAGAAATATGAATTCCTGCGTCG
>2.14|1503832|43|NZ_CP009285|CRISPRCasFinder
AAATTGCATAACGCTGAGATTCTTCGTTACGCCGACGGCGTCG
>2.15|1503900|41|NZ_CP009285|CRISPRCasFinder
AAATTGCGTATGTACCACGACCCGTGCGTCCAGTTCGGTCG
>2.16|1503966|43|NZ_CP009285|CRISPRCasFinder
AAATAGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCGGTCG
>2.17|1504034|43|NZ_CP009285|CRISPRCasFinder
AAATGATTCAAATGGCAGGAATTTGCATGGCAGGCTTTGGTCT
>2.18|1504102|43|NZ_CP009285|CRISPRCasFinder
AAATTTGGATGCTTCGAGCTCAGTAAGAGCCTTGCGCTTGTCG

CRISPR arrays and Neighbor proteins around NZ_CP009285_2

CRISPR arrays

The CRISPR arrays of NZ_CP009285_2

>merge|NZ_CP009285|2|1503533-1504173|PILER-CR,CRT,CRISPRCasFinder
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGTTTCAGCAGGTATATCCAATGACGATTCAGCAGGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATGACACCACGGAGTAAGAGCCACTACATGTCTGGGAAGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATACACAGAAGCAGATTGATGCGGGTTGGGCGGATCGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATACTGATGAAATAACCAAGAAATATGAATTCCTGCGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATTGCATAACGCTGAGATTCTTCGTTACGCCGACGGCGTCGCACTCCGTGTGGAATGTGTGGATTGAAATTGCGTATGTACCACGACCCGTGCGTCCAGTTCGGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATAGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCGGTCGCACTCCGTGTGGAGTGTGTGGATTGAAATGATTCAAATGGCAGGAATTTGCATGGCAGGCTTTGGTCTCACTCCGTGTGGAGTGTGTGGATTGAAATTTGGATGCTTCGAGCTCAGTAAGAGCCTTGCGCTTGTCGCACTCCGTGTGGAGTGCGTGGATTGGAAT

>NZ_CP009285|2|1|1503533-1504105|PILER-CR
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GTTTCAGCAGGTATATCCAATGACGATTCAGCAG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	GACACCACGGAGTAAGAGCCACTACATGTCTGGGAA
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	ACACAGAAGCAGATTGATGCGGGTTGGGCGGATC
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	ACTGATGAAATAACCAAGAAATATGAATTCCTGC
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	TGCATAACGCTGAGATTCTTCGTTACGCCGACGGC
GTCGCACTCCGTGTGGAATGTGTGGATTGAAAT	TGCGTATGTACCACGACCCGTGCGTCCAGTTCG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	AGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	GATTCAAATGGCAGGAATTTGCATGGCAGGCTTTG
GTCTCACTCCGTGTGGAGTGTGTGGATTGAAAT

>NZ_CP009285|2|1|1503533-1504173|CRT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GTTTCAGCAGGTATATCCAATGACGATTCAGCAG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	GACACCACGGAGTAAGAGCCACTACATGTCTGGGAA
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	ACACAGAAGCAGATTGATGCGGGTTGGGCGGATC
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	ACTGATGAAATAACCAAGAAATATGAATTCCTGC
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	TGCATAACGCTGAGATTCTTCGTTACGCCGACGGC
GTCGCACTCCGTGTGGAATGTGTGGATTGAAAT	TGCGTATGTACCACGACCCGTGCGTCCAGTTCG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	AGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCG
GTCGCACTCCGTGTGGAGTGTGTGGATTGAAAT	GATTCAAATGGCAGGAATTTGCATGGCAGGCTTTG
GTCTCACTCCGTGTGGAGTGTGTGGATTGAAAT	TTGGATGCTTCGAGCTCAGTAAGAGCCTTGCGCTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGGAAT

>NZ_CP009285|2|2|1503537-1504169|CRISPRCasFinder
CACTCCGTGTGGAGTGCGTGGATTG	AAATGTTTCAGCAGGTATATCCAATGACGATTCAGCAGGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATGACACCACGGAGTAAGAGCCACTACATGTCTGGGAAGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATACACAGAAGCAGATTGATGCGGGTTGGGCGGATCGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATACTGATGAAATAACCAAGAAATATGAATTCCTGCGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATTGCATAACGCTGAGATTCTTCGTTACGCCGACGGCGTCG
CACTCCGTGTGGAATGTGTGGATTG	AAATTGCGTATGTACCACGACCCGTGCGTCCAGTTCGGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATAGCCGTAGATCGGTGCCCGCGCCGTCTCACACCCGGTCG
CACTCCGTGTGGAGTGTGTGGATTG	AAATGATTCAAATGGCAGGAATTTGCATGGCAGGCTTTGGTCT
CACTCCGTGTGGAGTGTGTGGATTG	AAATTTGGATGCTTCGAGCTCAGTAAGAGCCTTGCGCTTGTCG
CACTCCGTGTGGAGTGCGTGGATTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW	unknown	unknown	gnl|CDD|223708
NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein	unknown	unknown	gnl|CDD|223728
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_CP009285.1|WP_042210960.1|1491997_1493353_+|radical-SAM-family-heme-chaperone-HemW	unknown	unknown	gnl|CDD|223708
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|379188
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase	unknown	unknown	gnl|CDD|223896
NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl|CDD|275178
NZ_CP009285.1|WP_042210967.1|1502345_1503152_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW	unknown	unknown	gnl|CDD|223708
NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_052429355.1|1493370_1493688_+|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl|CDD|223672
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|226175
NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl|CDD|275178
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|273040
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	1.4e-147	485.9	0.3
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	1.5e-127	419.4	0.3
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1.4e-59	196.0	0.0
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	2.4e-85	282.0	9.7
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	2.4e-33	110.5	1.3
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	2.8e-31	102.3	0.7
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	6.6e-159	524.6	1.8

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein	gnl|CDD|223728	COG0655, WrbA, Multimeric flavodoxin WrbA [General function prediction only].	8.83089e-34
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.50482e-92
NZ_CP009285.1|WP_042210960.1|1491997_1493353_+|radical-SAM-family-heme-chaperone-HemW	gnl|CDD|223708	COG0635, HemN, Coproporphyrinogen III oxidase and related Fe-S oxidoreductases [Coenzyme metabolism].	4.31609e-97
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	8.725e-08
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	2.84039e-75
NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase	gnl|CDD|223896	COG0826, COG0826, Collagenase and related proteases [Posttranslational modification, protein turnover, chaperones].	9.24047e-24
NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein	gnl|CDD|275178	TIGR04385, radical_SAM_superfamily_protein, putative variant cofactor biosynthesis B12-binding domain/radical SAM domain protein 1. Members of this protein family are one of two tandem B12-binding domain/radical SAM domain proteins that occur in a genome context with a pair of homologs to ThiC (phosphomethylpyrimidine synthase, EC 4.1.99.17), an enzyme that performs a complex rearrangement involved in thiamin biosynthesis, and a putative CobT (nicotinate-nucleotide--dimethylbenzimidazole phosphoribosyltransferase), an enzyme of cobalamin biosynthesis.	1.0736e-51
NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW	gnl|CDD|223708	COG0635, HemN, Coproporphyrinogen III oxidase and related Fe-S oxidoreductases [Coenzyme metabolism].	1.9317e-98
NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW	gnl|CDD|223708	COG0635, HemN, Coproporphyrinogen III oxidase and related Fe-S oxidoreductases [Coenzyme metabolism].	1.72291e-101
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|226175	COG3649, COG3649, CRISPR system related protein [Defense mechanisms].	1.02785e-134
NZ_CP009285.1|WP_052429355.1|1493370_1493688_+|carboxymuconolactone-decarboxylase-family-protein	gnl|CDD|223672	COG0599, COG0599, Uncharacterized homolog of gamma-carboxymuconolactone decarboxylase subunit [Function unknown].	4.94147e-11
NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	5.67281e-35
NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein	gnl|CDD|275178	TIGR04385, radical_SAM_superfamily_protein, putative variant cofactor biosynthesis B12-binding domain/radical SAM domain protein 1. Members of this protein family are one of two tandem B12-binding domain/radical SAM domain proteins that occur in a genome context with a pair of homologs to ThiC (phosphomethylpyrimidine synthase, EC 4.1.99.17), an enzyme that performs a complex rearrangement involved in thiamin biosynthesis, and a putative CobT (nicotinate-nucleotide--dimethylbenzimidazole phosphoribosyltransferase), an enzyme of cobalamin biosynthesis.	2.3056e-40
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	gnl|CDD|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	2.76046e-30
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.79564e-34
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	7.7654e-167

Protein sequences

>NZ_CP009285.1|WP_042210967.1|1502345_1503152_+|hypothetical-protein
MNSKVTKNIFYEDLQDAGKFKQLEKRLLGESNLPGPRANLGAASTFADAFGSDWVTGDAWELLVEWSSRAEADAPTDDPREFLPFCALQAMGTYYRYADSSRQQIILERCQAAMNDSRWRMREAAAMALQRIGEQDFGALRSLFDAMMGKASALEKRAFVATLAHPPMLKDAAHVLYALELSEHILDEIAEGKTRYGTEDFRVLSKGLEYALSVFVERAPEAGFRMLAKFAVTEDKRMQKIVKSNLGKARLAKKYSQDVERIQLLMNA
>NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW
MNKPVYPFREIGIGHYPMGNSPVTPEDSKHLPSMMNLNHAAPSSKLVYVHIPFCDSICPFCPYPKAFNEQTARQEYLTALFSELEIYGSAPQIRNCSVEALYIGGGTPSVLDEEEITALFEQLQATLPMQNIEEITFEGNPASFTAAKLKLLYALGVNRISLGVQTFNDELGRRLGLLQTSEDSLRTIQQSREAGISNVSLDLMYNLPGQSMEEWLEDLEKVVELGIGHVTLFPLKIIPGFGLAKRIASGELPPCGDLALEQQMYVEACRYLESHGYAVESTYDFVQPGGHHIYSRKHFDDHLDLLSVGLGAFGEVGGYAYQNVKLLPEYVKKITSGELPVSLGYQVTPEDLPNQFLAMGLRRTAIDRQLFRRKFGSFPEEHFPELFDKFVKAGLVDIREETIALTRFEGLFWGNNVCKEFCEEHIKIAFPK
>NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein
MRILVVSTNTLKKPMPVLPVGAGMVYSALTAAGFETRFLDLAFMAEPFAALRDELRVFEPELICLSVRNIDNQVIQQPESYLPFIREVMKVCRTCSSAKVLLGGAAMLVMPEELVEELGADYGIKGSGETEAVRLAHELERGQAAGRDKVVTAVPAYHPVYSRIPAKTLFSPQYFIPNPRIKKASMGYQASRGCSRHCIYCSEGYKNSGGCRIPAEQFMEDMKILQADYQVNSITFVDGVFNHDVEETMEFCGLIGRTSASLDWSCALTPANITEELVCLLKRSGCRFVDIGADSGSEQMLRRMGKQFHPEQLLELGRLLEQYQIPYSVSLLFGGPGEHEETMAETVQLVNQLNPVYILASQGIRIYPHTALYHTALQEQVIQKNDNLLVPAFYQSKDYSDALLNKVLAASRHIYKDMLMNSIGGRT
>NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein
MGRVLLISANTEKRPPVFPLGLSYIHASLVASGYEAGMLDMTQLDYTREAVTSYLDSYAPDYIGVSIRNLDNCCMQYPRSFVEQVCLLVDWVRQWSHAAIVILGGAGFSLLPRQWLQETGADYGIVGDGCDSMVELLSHLEKGEEPSAVSGLMFCTKNGEWKYSAPEAPEQLDHPYFPSRSGFLHSYDVERKVRHNVLTKRGCALSCTYCAYPSLEGRAVRLRSPQGIADEIEQMVLQHDIGSFDFVDSVFNYPLEHAEDICRELIGRAVPVSWGCFLNPRFFTAEFAGLLKQAGCTEVEFGIDSGSDICLRSFKKNFRQTEIRAVVQLCQEQDLAFSFCLLIGGPEETPETLRETLDLMEELKVQHIFGLFGIRILPSTDMYRYVGSPEPDDLLHPKFFMSPQLNLEQASSICRPYRERNPDWMFI
>NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase
MLKTKGIPLFYRCQGTGEAVLCLHGNRDSSLVFRELAQAMQPHYQVLCADLRGHGQSEYSGPPFTLEDMVDDIVRLLDEQGLKQVSIVGHSLGSTLALLLSARDPGRVKKLVLMGAAATFRVPFKRPGHGEEITPDTVKQTNAAAVPYFFTADHEEVQHLILEGWSRLPAATHRLMIQIKHPDLRPILQDIRQRTLIITGQEDRITPLPKALELNRYMPDSRMLAVPGTGHFMFLEESETVASAILTFLKEE
>NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein
MKKMIGLAGSMKKHHSSSEYLLSVALEAAEEQGVQTELLRLNDYNILPCEGCGNCMNGKPCHLLKKPEDQLTELYDKLKEADGFIFSSPVYALSLPAVWKNWIDRCEPCSAEDLDFEHYNYDRVAGVKGKAFKGKVAGQIVVAAGPGHEWALASLMPCFTAIKLSMIASAGISLIEYDGQPGIRKRSWSKPIEEAESAKMMARAVGLRVASALGFSYFDSPAEQGQVRWEQQQERAELAGAWSAFTVQNIRDEEVRLGELAEKQPHIFVIGDQQASSRCGPLLEQLEQQFGGRAACALIARVGQLPHFITHEFVKEKTGQAVPGFELYYDWEDALASRCSVAPGQPAILVGRTREEWQLFAVDGTQGREIGRVVDYLEEAIV
>NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase
MMKLSVGTNFDDRLPLLLKDSHVDVFYGKLSSDLVGGGRPTFALPTIDRTRVEEHVKLLHAYGFKFNYLLNATCLDNLETTKEFHYRLRELLEWIGTLQPEYVTVSLPMLVDMVRTALPDVKISLSTFANVNTLRQAHYFEERGVSEITLPESRNRDFSFLESLRKSTSCDYQLIATNDCLLDCPMRQNHANFQSHASQCNHVTDGFALDYYMLRCTERKLQHPEELLKSQWIRPEDMHIYEELGYHKFKLTERMKTTEKIADTALAYSGRSYQGNLLSLLNSRMAEADFEMPNFSKNIKEDFAPSEKMRQVYSLLFSFQANIDNESLEGFLEGFRAKRCDRMDCDKCGYCAEWASRTVQVAKPGGAVLREFEELFAALASGTFFESAAGAPVTWTAEGQSLYEGVVGRKPEFIRDMASTEIRKKAEELAAANGTGQVSRYDVAKANVLCTPADFRMFALMDLRSLGFDTAELDAEEAVG
>NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW
MAVKTSYEPFYNVYPHRDPICVSHYPNPVTEIAPADIYGVMDLNSQPPADNVGAVYVHVPFCASVCIFCPFNKMAYQEKQVEQYMEAVKAEIGIYASSPYASQSTISAVTFGGGTPSALSAERMVEMLKSVQEHYRVLPDAQISFEGSPATLTLEKMQAIRAQGANRISIGVQTFNDKMGRHLRMSHDSHRAFEVLNEAKEAGFDNIGIDLMYNLPEQTMEEWLEDVRTAVRLGIDHITVFSLCVVPFTALFKMIKEGTIPPTGDVNLEVDMYLEAKRLLQEEGYVQYSVWDFAKPGFEDRHVLLYYTQQKDLFAHGPAAFGYVNKLMYINQGDIQEYSSRLQQQFLSVFIASKADDLEAMHGMMAKGLRMLSVKRKDFAGMFGYQPEEVFGPTIDDLVSKGLLETDEHEIRLSAKGIVWGNNVCKEFFSEANQQTFESRVKLARGQKPAEVTGEVLK
>NZ_CP009285.1|WP_052429355.1|1493370_1493688_+|carboxymuconolactone-decarboxylase-family-protein
MSDMLMRVNPQVGTAFEGMCKAIEDTGTLEPKVRELVRLACVVTDRSTYGIRLHALKAYELGATPEEVTETVMNCLPVAGIEAVSSGLAAAMTALESKRGVHHGS
>NZ_CP009285.1|WP_042210960.1|1491997_1493353_+|radical-SAM-family-heme-chaperone-HemW
MSRAKQYVELFKERDSICVSHYPVPISQHTESEVWSLMELEQVNTKDTPTALYLHIPFCDATCSFCPFNRYLKKQEQVDDYLAAVRKEIDRYAGTPFGSSITVSSINLGGGTPSCLSSEELTGILQHMKQAFHVAEDAMIFIEGNPRNFTADKLEDLALQGLNRISVGVQTFQEELAGLLGLYHSVDDSFELVKNARSCGIDNIGIDLMYNLPGQTLDQWRADILTSIEQEIDHICVISFCVVPHTQIASRIAEGKIPGIGDVYREIELYTIAKEMLLEAGYLQYSVIDFAKPGKTDRHATLYFSEQSHMIGIGAAAFGIINGYMYVNSGNLNEYMSRVQDGLLPVNCGEKADELELAHGAMAKGLRMLSVSRADFVRMFRQEPEELFPDTIERLVQDGLLIQDAEGIRLTDDGIIWGNNVSKQFFSSKYADYGLQHRMKLAKGRPVQSVK
>NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator
MEFKDYTLYCKLDTILKAHDISVLKLSKEIGHRRTTIMELMHNTNMEKKKISAELIMKLCLYFEVTPNDLFEIRRKE
>NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein
MSKRRPRKLNVQAILDIIKKNLVWPELKGLPDAIHYYHLTDALGRKWQTIGCHVTDAIKVFKMGEYPPWTLIIESAPYDPHITVRELIAMLNCEDNALVNDMQIILNTTVRCNQFINVIVNVNYYSIFTVLYDLKNDYLLNDPIPISDFEAMYNINPIEALSRFYLENVDTLDYWVWVQAGGSAELAVNFRKANPTLTLIEAIEKLERMRDIT
>NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3
MDYIAHIRESDGRIQTVTEHLLEVRALAEAFGEKLGVRHIAGLAGVLHDLGKYTEEFREYILAAVNNPDAPPRRGSVDHSTAGGKLLFDWFHPSSPEYANERVSQTKAILAEIVGNAIISHHSYLQDFLNPDLESSYLKRVRDKHLEEFSSLTLKMFFEQVINEQEFRLYVDQAELELIAFLKKEPKVTLEHRAMLLSKFIFSALIDADRTNTRSFEANKNDDEVDHKVLFEQYYDRLITRINSFQTHKNADSEINRLRREMSEQCDAFANNGSGIYTLSIPTGGGKTLASVRYALKHARIFNKQRVIYVIPFTTIIEQNAAEVRKILMDDEHILEHHSNVVEAETEDDEQEDGKAVIGQKLKLAKDNWDAPVIFTTMVQFLNVFYADGSRNIRRLHNLSNAVIIFDEVQKVPVSCISLFNYAVNFLKTYANSSIVLCTATQPELDYVRYKLQLSPEAEMISSLDDVVKAFKRVDIIDRATGEQFNTDKLADFVLDKIQDVLSVLVILNTRSVVKALYNKLQEQDLSIPIYHLSTSMCAAHRKEILVEVKRLLEAKLPVICISTQLIEAGVDVSFKCVIRSLAGLDSIAQAAGRCNRHGEDEIQQVYVIDHSEEDLKKLKEIRVGKDKTRKILVDFCRDPVRLGGHLLSVQAMKQYFQEFYTELASSLNYNIPKLEKEMTGLLSADRVSNSFHSEYRSEHNASVPLYLHNSYKTAAEHFHVIDNHTTSVIVPYERGKEIIADLNGQHSIQDLSKLLREAQQFTINLFNFEKDTLGKINGIVPYLDGKVFALKEGTYSSEYGLDLKGESVMEVSLY
>NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein
MNNSTFSLVEDYPDYYKKKPVSKLQGFFSRSPELPSKQELSVESLLKKQRLRIGELQQENEILRKAMHLLTK
>NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGVVESIYWKPTLIIVVDEVRVMNAIRMESKGIRPMEYGGGNTLANYTYLKEPHYEVRAHFVFNENRPDLAHDRNEHKHHNILKRSLEAGGRRDIFLGARECQAYVEPCVFGEAPGYYDTYDGEIHFGNMVHGINYPDETGRDQMEVRLWNPVMKNGYIKFDKPEDCTKVRRIADMQPKLFDHHNVQSVDELFEEIEAGGQS
>NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYKANVDRVGEIETKHNDREYTLLPVSHTTQNAHITVEITEAGEFHSAIVNDKSDISTLIPCTEESSSRAGSKIAPYPLHDKLSYVAGDFVAYGGQIKKEEPFAAYIKQLEEWANSPYASPKVKSIYTYLSKRRLIQDLVAWRVIFLDANDKLIDKWDKKYEALHGEKPPIFTLVAGEQESAFVRFNVRKQNDHTMVWKDSEMFNSFVQHYSSLLGKEDFCYVTGEILPSTDRHANKIRNAGDKAKLISANDTSGFTFRGRFAQSSDAASISYEVSQKAHNALKWLINRQGKIIDQRVFLVWGNDDLDIPDPNADTFTLKLELEPEMEPELKPVAADVKISHTYKEYAREVAKALDGYRNRLASRSKSNVNILILDSATTGRLAVLYYRNMEKNLYVDQLIKWHSTCAWLHKYRKNEQGETATFYGAPSTKDVAFAAYGPKANEKVVKGMMERVLPCIVDGHKIPQDIVRSAFQRASNPVALESWEWEKTLSITCALINTREVYNVALDTENDDRSYLFGRLLAIADVLERRALDSDERRSTNAIRYMNSFSRYPARTWSTIQSCLLPHQARLGTRVRYYSNLIDEVASKIKIEEFDNKALTGKYLLGFYSQRHELNYGKAKSGDSNPTIPTSNHEER
>NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTTLDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDAGESIFVQSNDRKNDSFGSLRERADANPELDKILKAKTSSNEEFARIACQEWIDVRSFGQVFAFKADSKGSGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDYGLYVFYGSINTQLAEKTGFTNEDADKIKEALITLFANDVSSARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLDVRALKDEPKSIEDYSIEVYQLEGLQPEVMNGL
>NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4
MAYSDDDDALMLSGIQHFHFCKRQWALIHIEQQWAEDFRTIEGQHLHRNADQPFTREKRGDKLVVRAMPVKSRQLGITGICDVVEFIRDNSGVEINGAEGKYVAYPVEYKRGKPKLEDIDVLQLTAQAMCLEEMLLCDVRTGYIFYNEIKHRIEVPLTDELKLKVGSILEEMQDYYRRGYTPKVRTGAFCESCSLQHICLPKLMNKQTVKSYVEGKIRE
>NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLQNTLYITQPDVYLSLDGDNVVLLKEQEKLGRVPLHNLESIVAFGYTGASPALMGYCADNNVSLLFLTMNGRFLARVTGESRGNVILRKKQYALSEDETKSARIARNFIIGKIYNHKWILERTTRDYPLRVNVEQFKEASQQLSALILEVRNCEQLDRLRGFEGQAAITYNKLFDSMILQQKEDFQFHLRSRRPPLDNVNAMLSFSYTLLAHDTASALEAVGLDSYVGFLHRDRPGRVSLALDLMEELRGVMADKFVLTQINKKLVSKEDFVKKENGAVIMTDEARKRFLTAWQNRKQEKITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2
MLVLITYDVSTTSSAGQSRLRRVAKICQNYGQRVQNSVFECIVDAAQFTELKLKLKDIINLKEDSLRFYQLGNNYKNKVEHVGIKESLDLEGPLIL

Crispr_ID: NZ_CP009285_3

• CRISPR_ID: NZ_CP009285_3
• CRISPR_location: 1505623-1508086
• CRISPR_type: TypeI
• Repeat_type: NA
• Spacer_info: 36 spacers
• Cas_protein_info: cas3,cas5,cas8c,cas7,cas4,cas1,cas2

Consensus repeat of NZ_CP009285_3

Consensus_repeat	Method
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	PILER-CR
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CRT

spacers of NZ_CP009285_3

>3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGGATCTCCTGCAGGAACTTCCTGCAGAAAAATT
>3.2|1505723|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACCTTTGAAGAGACCACAAAGCATTTGGATATCC
>3.3|1505790|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GTCATATCTTGGACGGCATCCCATCCGGTCAGATT
>3.4|1505858|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTCAGGAGTTGTACCGTACCACGTAGTACCCAAATT
>3.5|1505927|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AATGAGGTCTTATACCTTTTATACGATGAGAT
>3.6|1505992|37|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACCTGTAGAAGTTACAAGAACAGCTTGATCTGGATAG
>3.7|1506062|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTGGATGGCAAGCAGATCGAAACCAATGTATCCCGC
>3.8|1506131|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CACCCGGACGTACCGGACGACTACATTGACGA
>3.9|1506196|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATTATTAAGCCTCCTTTAGGCAAGTCTGATAATGC
>3.10|1506264|37|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TCCGCATGATGGCAACCATTGCGCCATGGTCAGCAGC
>3.11|1506334|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CCTATTTAGAATCATGTCAATAGTGCGATAGTGTAC
>3.12|1506403|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GGATTACTCAAGAACTATGTAAACTATGTGGATCG
>3.13|1506471|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTGACCCGGCTATTTTTAATCGTGGTAGCCGTGAT
>3.14|1506539|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AATTGGACAAGGAGTGTGATTTTATGGCTGGGAG
>3.15|1506606|37|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGCCACCACATCTTATATGTGATACGTCCCTGTGTAC
>3.16|1506676|37|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACGGATGGTACGACAAGCAGTTTTGATACGCATTATC
>3.17|1506746|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTCCGCGTGTTGACAAATACGAAGTGAAGGACG
>3.18|1506812|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AAGGATGAACTGGACGCGCTTGGGGATATCTCCGT
>3.19|1506880|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AACGAGGCCGGTGCAGAATTACCTAAGTGGTATGA
>3.20|1506948|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATCCAGAAGACAACAAAGTCATCATTCAGCGGCC
>3.21|1507015|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATGGACACCGGCAATCATTGCAAGCTCGGCATCCCC
>3.22|1507084|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGCTCTGACGAGTCCTGCAGCGATAAGGGGCAGCAG
>3.23|1507153|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GGTGCTGTGCAATTGGGAGGCCAGGCACTTGGA
>3.24|1507219|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATCATCATAGTAGATAAGCACATGCTCATTTTT
>3.25|1507285|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTGACATACGAACTTGAACGGGATGCTAACGGAAA
>3.26|1507353|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GGAAGATACTGCATGAGGAAAAATTGGGCTTCAA
>3.27|1507420|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGCTCGTCATACAGAGTGCCGTCCGGTGCAAGGCT
>3.28|1507488|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AAGTAGCAGAGAGGCCCTGAAAAGTACCTGCGAT
>3.29|1507555|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GCAAAGCTCGTCCAGATCAAATGTACGCATAGTG
>3.30|1507622|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CCGCTTGAAGCAGTGCCGATATAGAGCTTGCTTG
>3.31|1507689|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TACCAGTGGGATGTACACTGACTCCTATCATA
>3.32|1507754|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TGCGTAGAGCGTGGGATTCCGATGCAGCAGCTGCT
>3.33|1507822|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AACGAGTGCGCCGGCGGGTACCTGCCATTGCTT
>3.34|1507888|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TCTATGCGTATGCAAATTTTGGAGTAACAGCGG
>3.35|1507954|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGACAAACCCCTTGGCAATATGCTTACTGACCT
>3.36|1508020|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GCTCCATCTACTGCCGCTTGAGTTTTCAGCGTTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_3

CRISPR arrays

The CRISPR arrays of NZ_CP009285_3

>merge|NZ_CP009285|3|1505623-1508086|PILER-CR,CRISPRCasFinder,CRT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCGGATCTCCTGCAGGAACTTCCTGCAGAAAAATTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATACCTTTGAAGAGACCACAAAGCATTTGGATATCCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGTCATATCTTGGACGGCATCCCATCCGGTCAGATTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTTCAGGAGTTGTACCGTACCACGTAGTACCCAAATTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAATGAGGTCTTATACCTTTTATACGATGAGATGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATACCTGTAGAAGTTACAAGAACAGCTTGATCTGGATAGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCTGGATGGCAAGCAGATCGAAACCAATGTATCCCGCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCACCCGGACGTACCGGACGACTACATTGACGAGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATATTATTAAGCCTCCTTTAGGCAAGTCTGATAATGCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTCCGCATGATGGCAACCATTGCGCCATGGTCAGCAGCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCCTATTTAGAATCATGTCAATAGTGCGATAGTGTACGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGGATTACTCAAGAACTATGTAAACTATGTGGATCGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCTGACCCGGCTATTTTTAATCGTGGTAGCCGTGATGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAATTGGACAAGGAGTGTGATTTTATGGCTGGGAGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCGCCACCACATCTTATATGTGATACGTCCCTGTGTACGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATACGGATGGTACGACAAGCAGTTTTGATACGCATTATCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTTCCGCGTGTTGACAAATACGAAGTGAAGGACGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAAGGATGAACTGGACGCGCTTGGGGATATCTCCGTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAACGAGGCCGGTGCAGAATTACCTAAGTGGTATGAGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATATCCAGAAGACAACAAAGTCATCATTCAGCGGCCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATATGGACACCGGCAATCATTGCAAGCTCGGCATCCCCGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAGCTCTGACGAGTCCTGCAGCGATAAGGGGCAGCAGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGGTGCTGTGCAATTGGGAGGCCAGGCACTTGGAGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATATCATCATAGTAGATAAGCACATGCTCATTTTTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCTGACATACGAACTTGAACGGGATGCTAACGGAAAGTCGCACTTCGTGTGGAGTGCGTGGATTGAAATGGAAGATACTGCATGAGGAAAAATTGGGCTTCAAGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAGCTCGTCATACAGAGTGCCGTCCGGTGCAAGGCTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAAGTAGCAGAGAGGCCCTGAAAAGTACCTGCGATGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGCAAAGCTCGTCCAGATCAAATGTACGCATAGTGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATCCGCTTGAAGCAGTGCCGATATAGAGCTTGCTTGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTACCAGTGGGATGTACACTGACTCCTATCATAGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTGCGTAGAGCGTGGGATTCCGATGCAGCAGCTGCTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAACGAGTGCGCCGGCGGGTACCTGCCATTGCTTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATTCTATGCGTATGCAAATTTTGGAGTAACAGCGGGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATAGACAAACCCCTTGGCAATATGCTTACTGACCTGTCGCACTCCGTGTGGAGTGCGTGGATTGAAATGCTCCATCTACTGCCGCTTGAGTTTTCAGCGTTTGTCGCACTCCGTGTGGAGTACGTGTATTGAAAT

>NZ_CP009285|3|2|1505623-1508086|PILER-CR
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGGATCTCCTGCAGGAACTTCCTGCAGAAAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTTTGAAGAGACCACAAAGCATTTGGATATCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GTCATATCTTGGACGGCATCCCATCCGGTCAGATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCAGGAGTTGTACCGTACCACGTAGTACCCAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATGAGGTCTTATACCTTTTATACGATGAGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTGTAGAAGTTACAAGAACAGCTTGATCTGGATAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGGATGGCAAGCAGATCGAAACCAATGTATCCCGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CACCCGGACGTACCGGACGACTACATTGACGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATTATTAAGCCTCCTTTAGGCAAGTCTGATAATGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCCGCATGATGGCAACCATTGCGCCATGGTCAGCAGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCTATTTAGAATCATGTCAATAGTGCGATAGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGATTACTCAAGAACTATGTAAACTATGTGGATCG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACCCGGCTATTTTTAATCGTGGTAGCCGTGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATTGGACAAGGAGTGTGATTTTATGGCTGGGAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGCCACCACATCTTATATGTGATACGTCCCTGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACGGATGGTACGACAAGCAGTTTTGATACGCATTATC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCCGCGTGTTGACAAATACGAAGTGAAGGACG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGGATGAACTGGACGCGCTTGGGGATATCTCCGT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGGCCGGTGCAGAATTACCTAAGTGGTATGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCCAGAAGACAACAAAGTCATCATTCAGCGGCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATGGACACCGGCAATCATTGCAAGCTCGGCATCCCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCTGACGAGTCCTGCAGCGATAAGGGGCAGCAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGTGCTGTGCAATTGGGAGGCCAGGCACTTGGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCATCATAGTAGATAAGCACATGCTCATTTTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACATACGAACTTGAACGGGATGCTAACGGAAA
GTCGCACTTCGTGTGGAGTGCGTGGATTGAAAT	GGAAGATACTGCATGAGGAAAAATTGGGCTTCAA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCGTCATACAGAGTGCCGTCCGGTGCAAGGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGTAGCAGAGAGGCCCTGAAAAGTACCTGCGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCAAAGCTCGTCCAGATCAAATGTACGCATAGTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCGCTTGAAGCAGTGCCGATATAGAGCTTGCTTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TACCAGTGGGATGTACACTGACTCCTATCATA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TGCGTAGAGCGTGGGATTCCGATGCAGCAGCTGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGTGCGCCGGCGGGTACCTGCCATTGCTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCTATGCGTATGCAAATTTTGGAGTAACAGCGG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGACAAACCCCTTGGCAATATGCTTACTGACCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCTCCATCTACTGCCGCTTGAGTTTTCAGCGTTT
GTCGCACTCCGTGTGGAGTACGTGTATTGAAAT

>NZ_CP009285|3|3|1505623-1508086|CRISPRCasFinder
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGGATCTCCTGCAGGAACTTCCTGCAGAAAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTTTGAAGAGACCACAAAGCATTTGGATATCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GTCATATCTTGGACGGCATCCCATCCGGTCAGATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCAGGAGTTGTACCGTACCACGTAGTACCCAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATGAGGTCTTATACCTTTTATACGATGAGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTGTAGAAGTTACAAGAACAGCTTGATCTGGATAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGGATGGCAAGCAGATCGAAACCAATGTATCCCGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CACCCGGACGTACCGGACGACTACATTGACGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATTATTAAGCCTCCTTTAGGCAAGTCTGATAATGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCCGCATGATGGCAACCATTGCGCCATGGTCAGCAGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCTATTTAGAATCATGTCAATAGTGCGATAGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGATTACTCAAGAACTATGTAAACTATGTGGATCG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACCCGGCTATTTTTAATCGTGGTAGCCGTGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATTGGACAAGGAGTGTGATTTTATGGCTGGGAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGCCACCACATCTTATATGTGATACGTCCCTGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACGGATGGTACGACAAGCAGTTTTGATACGCATTATC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCCGCGTGTTGACAAATACGAAGTGAAGGACG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGGATGAACTGGACGCGCTTGGGGATATCTCCGT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGGCCGGTGCAGAATTACCTAAGTGGTATGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCCAGAAGACAACAAAGTCATCATTCAGCGGCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATGGACACCGGCAATCATTGCAAGCTCGGCATCCCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCTGACGAGTCCTGCAGCGATAAGGGGCAGCAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGTGCTGTGCAATTGGGAGGCCAGGCACTTGGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCATCATAGTAGATAAGCACATGCTCATTTTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACATACGAACTTGAACGGGATGCTAACGGAAA
GTCGCACTTCGTGTGGAGTGCGTGGATTGAAAT	GGAAGATACTGCATGAGGAAAAATTGGGCTTCAA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCGTCATACAGAGTGCCGTCCGGTGCAAGGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGTAGCAGAGAGGCCCTGAAAAGTACCTGCGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCAAAGCTCGTCCAGATCAAATGTACGCATAGTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCGCTTGAAGCAGTGCCGATATAGAGCTTGCTTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TACCAGTGGGATGTACACTGACTCCTATCATA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TGCGTAGAGCGTGGGATTCCGATGCAGCAGCTGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGTGCGCCGGCGGGTACCTGCCATTGCTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCTATGCGTATGCAAATTTTGGAGTAACAGCGG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGACAAACCCCTTGGCAATATGCTTACTGACCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCTCCATCTACTGCCGCTTGAGTTTTCAGCGTTT
GTCGCACTCCGTGTGGAGTACGTGTATTGAAAT

>NZ_CP009285|3|2|1505623-1508086|CRT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGGATCTCCTGCAGGAACTTCCTGCAGAAAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTTTGAAGAGACCACAAAGCATTTGGATATCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GTCATATCTTGGACGGCATCCCATCCGGTCAGATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCAGGAGTTGTACCGTACCACGTAGTACCCAAATT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATGAGGTCTTATACCTTTTATACGATGAGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACCTGTAGAAGTTACAAGAACAGCTTGATCTGGATAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGGATGGCAAGCAGATCGAAACCAATGTATCCCGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CACCCGGACGTACCGGACGACTACATTGACGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATTATTAAGCCTCCTTTAGGCAAGTCTGATAATGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCCGCATGATGGCAACCATTGCGCCATGGTCAGCAGC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCTATTTAGAATCATGTCAATAGTGCGATAGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGATTACTCAAGAACTATGTAAACTATGTGGATCG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACCCGGCTATTTTTAATCGTGGTAGCCGTGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AATTGGACAAGGAGTGTGATTTTATGGCTGGGAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CGCCACCACATCTTATATGTGATACGTCCCTGTGTAC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ACGGATGGTACGACAAGCAGTTTTGATACGCATTATC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TTCCGCGTGTTGACAAATACGAAGTGAAGGACG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGGATGAACTGGACGCGCTTGGGGATATCTCCGT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGGCCGGTGCAGAATTACCTAAGTGGTATGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCCAGAAGACAACAAAGTCATCATTCAGCGGCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATGGACACCGGCAATCATTGCAAGCTCGGCATCCCC
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCTGACGAGTCCTGCAGCGATAAGGGGCAGCAG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GGTGCTGTGCAATTGGGAGGCCAGGCACTTGGA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	ATCATCATAGTAGATAAGCACATGCTCATTTTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CTGACATACGAACTTGAACGGGATGCTAACGGAAA
GTCGCACTTCGTGTGGAGTGCGTGGATTGAAAT	GGAAGATACTGCATGAGGAAAAATTGGGCTTCAA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGCTCGTCATACAGAGTGCCGTCCGGTGCAAGGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AAGTAGCAGAGAGGCCCTGAAAAGTACCTGCGAT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCAAAGCTCGTCCAGATCAAATGTACGCATAGTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	CCGCTTGAAGCAGTGCCGATATAGAGCTTGCTTG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TACCAGTGGGATGTACACTGACTCCTATCATA
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TGCGTAGAGCGTGGGATTCCGATGCAGCAGCTGCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AACGAGTGCGCCGGCGGGTACCTGCCATTGCTT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	TCTATGCGTATGCAAATTTTGGAGTAACAGCGG
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	AGACAAACCCCTTGGCAATATGCTTACTGACCT
GTCGCACTCCGTGTGGAGTGCGTGGATTGAAAT	GCTCCATCTACTGCCGCTTGAGTTTTCAGCGTTT
GTCGCACTCCGTGTGGAGTACGTGTATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW	unknown	unknown	gnl|CDD|223708
NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein	unknown	unknown	gnl|CDD|223728
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|379188
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase	unknown	unknown	gnl|CDD|223896
NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl|CDD|275178
NZ_CP009285.1|WP_042210967.1|1502345_1503152_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW	unknown	unknown	gnl|CDD|223708
NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|226175
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl|CDD|275178
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|273040
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	1.4e-147	485.9	0.3
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	1.5e-127	419.4	0.3
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1.4e-59	196.0	0.0
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	2.4e-85	282.0	9.7
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	2.4e-33	110.5	1.3
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	2.8e-31	102.3	0.7
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	6.6e-159	524.6	1.8

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein	gnl|CDD|223728	COG0655, WrbA, Multimeric flavodoxin WrbA [General function prediction only].	8.83089e-34
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.50482e-92
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	8.725e-08
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	5.27896e-19
NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase	gnl|CDD|223896	COG0826, COG0826, Collagenase and related proteases [Posttranslational modification, protein turnover, chaperones].	9.24047e-24
NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein	gnl|CDD|275178	TIGR04385, radical_SAM_superfamily_protein, putative variant cofactor biosynthesis B12-binding domain/radical SAM domain protein 1. Members of this protein family are one of two tandem B12-binding domain/radical SAM domain proteins that occur in a genome context with a pair of homologs to ThiC (phosphomethylpyrimidine synthase, EC 4.1.99.17), an enzyme that performs a complex rearrangement involved in thiamin biosynthesis, and a putative CobT (nicotinate-nucleotide--dimethylbenzimidazole phosphoribosyltransferase), an enzyme of cobalamin biosynthesis.	1.0736e-51
NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW	gnl|CDD|223708	COG0635, HemN, Coproporphyrinogen III oxidase and related Fe-S oxidoreductases [Coenzyme metabolism].	1.9317e-98
NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW	gnl|CDD|223708	COG0635, HemN, Coproporphyrinogen III oxidase and related Fe-S oxidoreductases [Coenzyme metabolism].	1.72291e-101
NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	5.67281e-35
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	3.08255e-54
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|226175	COG3649, COG3649, CRISPR system related protein [Defense mechanisms].	1.02785e-134
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	2.84039e-75
NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein	gnl|CDD|275178	TIGR04385, radical_SAM_superfamily_protein, putative variant cofactor biosynthesis B12-binding domain/radical SAM domain protein 1. Members of this protein family are one of two tandem B12-binding domain/radical SAM domain proteins that occur in a genome context with a pair of homologs to ThiC (phosphomethylpyrimidine synthase, EC 4.1.99.17), an enzyme that performs a complex rearrangement involved in thiamin biosynthesis, and a putative CobT (nicotinate-nucleotide--dimethylbenzimidazole phosphoribosyltransferase), an enzyme of cobalamin biosynthesis.	2.3056e-40
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	gnl|CDD|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	2.76046e-30
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.79564e-34
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	7.7654e-167

Protein sequences

>NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein
MSKRRPRKLNVQAILDIIKKNLVWPELKGLPDAIHYYHLTDALGRKWQTIGCHVTDAIKVFKMGEYPPWTLIIESAPYDPHITVRELIAMLNCEDNALVNDMQIILNTTVRCNQFINVIVNVNYYSIFTVLYDLKNDYLLNDPIPISDFEAMYNINPIEALSRFYLENVDTLDYWVWVQAGGSAELAVNFRKANPTLTLIEAIEKLERMRDIT
>NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator
MEFKDYTLYCKLDTILKAHDISVLKLSKEIGHRRTTIMELMHNTNMEKKKISAELIMKLCLYFEVTPNDLFEIRRKE
>NZ_CP009285.1|WP_042210967.1|1502345_1503152_+|hypothetical-protein
MNSKVTKNIFYEDLQDAGKFKQLEKRLLGESNLPGPRANLGAASTFADAFGSDWVTGDAWELLVEWSSRAEADAPTDDPREFLPFCALQAMGTYYRYADSSRQQIILERCQAAMNDSRWRMREAAAMALQRIGEQDFGALRSLFDAMMGKASALEKRAFVATLAHPPMLKDAAHVLYALELSEHILDEIAEGKTRYGTEDFRVLSKGLEYALSVFVERAPEAGFRMLAKFAVTEDKRMQKIVKSNLGKARLAKKYSQDVERIQLLMNA
>NZ_CP009285.1|WP_042210966.1|1501034_1502333_+|radical-SAM-family-heme-chaperone-HemW
MNKPVYPFREIGIGHYPMGNSPVTPEDSKHLPSMMNLNHAAPSSKLVYVHIPFCDSICPFCPYPKAFNEQTARQEYLTALFSELEIYGSAPQIRNCSVEALYIGGGTPSVLDEEEITALFEQLQATLPMQNIEEITFEGNPASFTAAKLKLLYALGVNRISLGVQTFNDELGRRLGLLQTSEDSLRTIQQSREAGISNVSLDLMYNLPGQSMEEWLEDLEKVVELGIGHVTLFPLKIIPGFGLAKRIASGELPPCGDLALEQQMYVEACRYLESHGYAVESTYDFVQPGGHHIYSRKHFDDHLDLLSVGLGAFGEVGGYAYQNVKLLPEYVKKITSGELPVSLGYQVTPEDLPNQFLAMGLRRTAIDRQLFRRKFGSFPEEHFPELFDKFVKAGLVDIREETIALTRFEGLFWGNNVCKEFCEEHIKIAFPK
>NZ_CP009285.1|WP_042210965.1|1499746_1501030_+|B12-binding-domain-containing-radical-SAM-protein
MRILVVSTNTLKKPMPVLPVGAGMVYSALTAAGFETRFLDLAFMAEPFAALRDELRVFEPELICLSVRNIDNQVIQQPESYLPFIREVMKVCRTCSSAKVLLGGAAMLVMPEELVEELGADYGIKGSGETEAVRLAHELERGQAAGRDKVVTAVPAYHPVYSRIPAKTLFSPQYFIPNPRIKKASMGYQASRGCSRHCIYCSEGYKNSGGCRIPAEQFMEDMKILQADYQVNSITFVDGVFNHDVEETMEFCGLIGRTSASLDWSCALTPANITEELVCLLKRSGCRFVDIGADSGSEQMLRRMGKQFHPEQLLELGRLLEQYQIPYSVSLLFGGPGEHEETMAETVQLVNQLNPVYILASQGIRIYPHTALYHTALQEQVIQKNDNLLVPAFYQSKDYSDALLNKVLAASRHIYKDMLMNSIGGRT
>NZ_CP009285.1|WP_042210964.1|1498436_1499720_+|B12-binding-domain-containing-radical-SAM-protein
MGRVLLISANTEKRPPVFPLGLSYIHASLVASGYEAGMLDMTQLDYTREAVTSYLDSYAPDYIGVSIRNLDNCCMQYPRSFVEQVCLLVDWVRQWSHAAIVILGGAGFSLLPRQWLQETGADYGIVGDGCDSMVELLSHLEKGEEPSAVSGLMFCTKNGEWKYSAPEAPEQLDHPYFPSRSGFLHSYDVERKVRHNVLTKRGCALSCTYCAYPSLEGRAVRLRSPQGIADEIEQMVLQHDIGSFDFVDSVFNYPLEHAEDICRELIGRAVPVSWGCFLNPRFFTAEFAGLLKQAGCTEVEFGIDSGSDICLRSFKKNFRQTEIRAVVQLCQEQDLAFSFCLLIGGPEETPETLRETLDLMEELKVQHIFGLFGIRILPSTDMYRYVGSPEPDDLLHPKFFMSPQLNLEQASSICRPYRERNPDWMFI
>NZ_CP009285.1|WP_081971929.1|1497676_1498435_+|alpha/beta-hydrolase
MLKTKGIPLFYRCQGTGEAVLCLHGNRDSSLVFRELAQAMQPHYQVLCADLRGHGQSEYSGPPFTLEDMVDDIVRLLDEQGLKQVSIVGHSLGSTLALLLSARDPGRVKKLVLMGAAATFRVPFKRPGHGEEITPDTVKQTNAAAVPYFFTADHEEVQHLILEGWSRLPAATHRLMIQIKHPDLRPILQDIRQRTLIITGQEDRITPLPKALELNRYMPDSRMLAVPGTGHFMFLEESETVASAILTFLKEE
>NZ_CP009285.1|WP_052429356.1|1496489_1497638_+|flavodoxin-family-protein
MKKMIGLAGSMKKHHSSSEYLLSVALEAAEEQGVQTELLRLNDYNILPCEGCGNCMNGKPCHLLKKPEDQLTELYDKLKEADGFIFSSPVYALSLPAVWKNWIDRCEPCSAEDLDFEHYNYDRVAGVKGKAFKGKVAGQIVVAAGPGHEWALASLMPCFTAIKLSMIASAGISLIEYDGQPGIRKRSWSKPIEEAESAKMMARAVGLRVASALGFSYFDSPAEQGQVRWEQQQERAELAGAWSAFTVQNIRDEEVRLGELAEKQPHIFVIGDQQASSRCGPLLEQLEQQFGGRAACALIARVGQLPHFITHEFVKEKTGQAVPGFELYYDWEDALASRCSVAPGQPAILVGRTREEWQLFAVDGTQGREIGRVVDYLEEAIV
>NZ_CP009285.1|WP_157763984.1|1495050_1496493_+|U32-family-peptidase
MMKLSVGTNFDDRLPLLLKDSHVDVFYGKLSSDLVGGGRPTFALPTIDRTRVEEHVKLLHAYGFKFNYLLNATCLDNLETTKEFHYRLRELLEWIGTLQPEYVTVSLPMLVDMVRTALPDVKISLSTFANVNTLRQAHYFEERGVSEITLPESRNRDFSFLESLRKSTSCDYQLIATNDCLLDCPMRQNHANFQSHASQCNHVTDGFALDYYMLRCTERKLQHPEELLKSQWIRPEDMHIYEELGYHKFKLTERMKTTEKIADTALAYSGRSYQGNLLSLLNSRMAEADFEMPNFSKNIKEDFAPSEKMRQVYSLLFSFQANIDNESLEGFLEGFRAKRCDRMDCDKCGYCAEWASRTVQVAKPGGAVLREFEELFAALASGTFFESAAGAPVTWTAEGQSLYEGVVGRKPEFIRDMASTEIRKKAEELAAANGTGQVSRYDVAKANVLCTPADFRMFALMDLRSLGFDTAELDAEEAVG
>NZ_CP009285.1|WP_042210961.1|1493677_1495054_+|radical-SAM-family-heme-chaperone-HemW
MAVKTSYEPFYNVYPHRDPICVSHYPNPVTEIAPADIYGVMDLNSQPPADNVGAVYVHVPFCASVCIFCPFNKMAYQEKQVEQYMEAVKAEIGIYASSPYASQSTISAVTFGGGTPSALSAERMVEMLKSVQEHYRVLPDAQISFEGSPATLTLEKMQAIRAQGANRISIGVQTFNDKMGRHLRMSHDSHRAFEVLNEAKEAGFDNIGIDLMYNLPEQTMEEWLEDVRTAVRLGIDHITVFSLCVVPFTALFKMIKEGTIPPTGDVNLEVDMYLEAKRLLQEEGYVQYSVWDFAKPGFEDRHVLLYYTQQKDLFAHGPAAFGYVNKLMYINQGDIQEYSSRLQQQFLSVFIASKADDLEAMHGMMAKGLRMLSVKRKDFAGMFGYQPEEVFGPTIDDLVSKGLLETDEHEIRLSAKGIVWGNNVCKEFFSEANQQTFESRVKLARGQKPAEVTGEVLK
>NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3
MDYIAHIRESDGRIQTVTEHLLEVRALAEAFGEKLGVRHIAGLAGVLHDLGKYTEEFREYILAAVNNPDAPPRRGSVDHSTAGGKLLFDWFHPSSPEYANERVSQTKAILAEIVGNAIISHHSYLQDFLNPDLESSYLKRVRDKHLEEFSSLTLKMFFEQVINEQEFRLYVDQAELELIAFLKKEPKVTLEHRAMLLSKFIFSALIDADRTNTRSFEANKNDDEVDHKVLFEQYYDRLITRINSFQTHKNADSEINRLRREMSEQCDAFANNGSGIYTLSIPTGGGKTLASVRYALKHARIFNKQRVIYVIPFTTIIEQNAAEVRKILMDDEHILEHHSNVVEAETEDDEQEDGKAVIGQKLKLAKDNWDAPVIFTTMVQFLNVFYADGSRNIRRLHNLSNAVIIFDEVQKVPVSCISLFNYAVNFLKTYANSSIVLCTATQPELDYVRYKLQLSPEAEMISSLDDVVKAFKRVDIIDRATGEQFNTDKLADFVLDKIQDVLSVLVILNTRSVVKALYNKLQEQDLSIPIYHLSTSMCAAHRKEILVEVKRLLEAKLPVICISTQLIEAGVDVSFKCVIRSLAGLDSIAQAAGRCNRHGEDEIQQVYVIDHSEEDLKKLKEIRVGKDKTRKILVDFCRDPVRLGGHLLSVQAMKQYFQEFYTELASSLNYNIPKLEKEMTGLLSADRVSNSFHSEYRSEHNASVPLYLHNSYKTAAEHFHVIDNHTTSVIVPYERGKEIIADLNGQHSIQDLSKLLREAQQFTINLFNFEKDTLGKINGIVPYLDGKVFALKEGTYSSEYGLDLKGESVMEVSLY
>NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein
MNNSTFSLVEDYPDYYKKKPVSKLQGFFSRSPELPSKQELSVESLLKKQRLRIGELQQENEILRKAMHLLTK
>NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGVVESIYWKPTLIIVVDEVRVMNAIRMESKGIRPMEYGGGNTLANYTYLKEPHYEVRAHFVFNENRPDLAHDRNEHKHHNILKRSLEAGGRRDIFLGARECQAYVEPCVFGEAPGYYDTYDGEIHFGNMVHGINYPDETGRDQMEVRLWNPVMKNGYIKFDKPEDCTKVRRIADMQPKLFDHHNVQSVDELFEEIEAGGQS
>NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYKANVDRVGEIETKHNDREYTLLPVSHTTQNAHITVEITEAGEFHSAIVNDKSDISTLIPCTEESSSRAGSKIAPYPLHDKLSYVAGDFVAYGGQIKKEEPFAAYIKQLEEWANSPYASPKVKSIYTYLSKRRLIQDLVAWRVIFLDANDKLIDKWDKKYEALHGEKPPIFTLVAGEQESAFVRFNVRKQNDHTMVWKDSEMFNSFVQHYSSLLGKEDFCYVTGEILPSTDRHANKIRNAGDKAKLISANDTSGFTFRGRFAQSSDAASISYEVSQKAHNALKWLINRQGKIIDQRVFLVWGNDDLDIPDPNADTFTLKLELEPEMEPELKPVAADVKISHTYKEYAREVAKALDGYRNRLASRSKSNVNILILDSATTGRLAVLYYRNMEKNLYVDQLIKWHSTCAWLHKYRKNEQGETATFYGAPSTKDVAFAAYGPKANEKVVKGMMERVLPCIVDGHKIPQDIVRSAFQRASNPVALESWEWEKTLSITCALINTREVYNVALDTENDDRSYLFGRLLAIADVLERRALDSDERRSTNAIRYMNSFSRYPARTWSTIQSCLLPHQARLGTRVRYYSNLIDEVASKIKIEEFDNKALTGKYLLGFYSQRHELNYGKAKSGDSNPTIPTSNHEER
>NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTTLDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDAGESIFVQSNDRKNDSFGSLRERADANPELDKILKAKTSSNEEFARIACQEWIDVRSFGQVFAFKADSKGSGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDYGLYVFYGSINTQLAEKTGFTNEDADKIKEALITLFANDVSSARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLDVRALKDEPKSIEDYSIEVYQLEGLQPEVMNGL
>NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4
MAYSDDDDALMLSGIQHFHFCKRQWALIHIEQQWAEDFRTIEGQHLHRNADQPFTREKRGDKLVVRAMPVKSRQLGITGICDVVEFIRDNSGVEINGAEGKYVAYPVEYKRGKPKLEDIDVLQLTAQAMCLEEMLLCDVRTGYIFYNEIKHRIEVPLTDELKLKVGSILEEMQDYYRRGYTPKVRTGAFCESCSLQHICLPKLMNKQTVKSYVEGKIRE
>NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLQNTLYITQPDVYLSLDGDNVVLLKEQEKLGRVPLHNLESIVAFGYTGASPALMGYCADNNVSLLFLTMNGRFLARVTGESRGNVILRKKQYALSEDETKSARIARNFIIGKIYNHKWILERTTRDYPLRVNVEQFKEASQQLSALILEVRNCEQLDRLRGFEGQAAITYNKLFDSMILQQKEDFQFHLRSRRPPLDNVNAMLSFSYTLLAHDTASALEAVGLDSYVGFLHRDRPGRVSLALDLMEELRGVMADKFVLTQINKKLVSKEDFVKKENGAVIMTDEARKRFLTAWQNRKQEKITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2
MLVLITYDVSTTSSAGQSRLRRVAKICQNYGQRVQNSVFECIVDAAQFTELKLKLKDIINLKEDSLRFYQLGNNYKNKVEHVGIKESLDLEGPLIL
>NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein
MGPSDTSAQRQAKWIKRFLRTYWLVIALHFAAQLWAFLFLSYPMGPHEFYYDVLLYPTLLMSAVVGLTQFVDAIAPKYSFVLLFVSGTIIAMMIIHLNMDIRIIGALMLLPIFASAIFFRLDLTLFTSALQAAAFFILYRWDYWFKYYLNDFDLIAVPLFLLVGTLVAGIIIINGRELASDLEATLTAKQNLMIENAVIRKLSTTDALTGLYNHISFHEFYEKALEYGNQGAPFHLALIDIDNFKRINDKYGHRTGDAVLARVAKVIKENISPADIASRYGGEEFAILFFEKSYEEAYELADRVRQQLSETLHEELENTAVTVSIGLKSYSEGATKEQLFEEVDELLYTAKKSGKNTTLTPLQQTRHLQSV
>NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein
MLWEDFINSYWRNWRTGDRSTDRDRLDEPEWLTRWLEQQKLPAAGPILPVELERLKQLRGLLWDEVQRLVQGQPTESALLEQLNEYMSNGPVMRQVVWSPGGEAGISLLPQRADWEQIMAEIAASFAEALLEKESSRFRICGNPDCLWVYYDDTRNRSKRYCDDKLCGNLMKVRRFRARRKAAEDEGNLPD

Crispr_ID: NZ_CP009285_4

• CRISPR_ID: NZ_CP009285_4
• CRISPR_location: 1517067-1520281
• CRISPR_type: TypeI
• Repeat_type: NA:I-C
• Spacer_info: 48 spacers
• Cas_protein_info: cas2,cas1,cas4,cas7,cas8c,cas5,cas3

Consensus repeat of NZ_CP009285_4

Consensus_repeat	Method
GTCGCTCCTCGTGCAG-GAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CRT

spacers of NZ_CP009285_4

>4.1|1517099|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TCGGTAGTCAGTTTTTAAACAATAATGGCGGGGTT
>4.2|1517166|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TCCAGGAGACCGCGACCTAGATCGGCTGCCCGCGCC
>4.3|1517234|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGGTCATGAATCACGGGAACCGGCAGTACTACTA
>4.4|1517300|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATTGCCGCTTGTTGAATGGCTATGGTCTGCTTTGC
>4.5|1517367|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGATCCCACCGGAGTTAGTAGATGCTTTTCCAG
>4.6|1517432|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACATTATTTTGATAACATTGATACCGAAGAAA
>4.7|1517496|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATTGATAATTTAAAACGCCATGCGAAAGCATGTTG
>4.8|1517563|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTACACACAGGGTGGGGATTTGTCTCAGACACATG
>4.9|1517630|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TGAAGAGGCGCATTCCGCTAATCCGGCCGATTTG
>4.10|1517696|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGAAAGTCGTCGGAATACGAGGAACTACCGCCAGA
>4.11|1517763|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATAGAATCACTTTTGACTCAGGAATCACTAATT
>4.12|1517828|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TCCAGGTGAATGGTGCACAGCGGATGATGCTATTC
>4.13|1517895|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CATCCAGCGCTCTTAAATTGCTTTGCGGCGCTAG
>4.14|1517961|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GTTAAAACGATGACCGCCTCTGACCGGATGTTTC
>4.15|1518027|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TGAGCTGCGAACCGTTACTTGGTCAGGTTGATCTA
>4.16|1518094|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GTTCAGGGGGATATATGTTGGCTGTTGGAGATGAA
>4.17|1518161|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AAACACCGGCGTCCGGAGCATCCCAGATTTGGTCC
>4.18|1518228|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTACGGTTGGAGGTTTGCATTAAATGTTGGTTTTT
>4.19|1518295|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CCGTCAACAGTGTTACCAGCACTGTATCGGGGTTGG
>4.20|1518363|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AACTTTTGCGCAGTGAATCAGCACCGCTTTCGGGT
>4.21|1518430|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTTTTACCCTTGAACATTCCAGCAACCGAGTCC
>4.22|1518495|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGTTTCACCGCGGACTTTGCGCATTACAACGCG
>4.23|1518560|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATTCCGGTAGGCGTGTGCTTGGGCATCATGACCAC
>4.24|1518627|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GATCTGCAGTTGCAGCGCGTCACCTGCGGTACCAC
>4.25|1518694|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGAAACTTGCTCTCATGGATCCAGCACTAAGCCT
>4.26|1518760|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACCAAGAGTCAAACTATGAAATATCTGGAGAGAGC
>4.27|1518827|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATGAGGGTACACAAGAATGCGAAATGGTTCAGGT
>4.28|1518893|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTCGCTGTCTCGGCTGTATGTGGCTTTGATCTC
>4.29|1518958|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTATAGGGAATGAGGTAAGCATGACCGAGGATA
>4.30|1519023|37|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GTACCTGCCGACGCTGTGGGCGCTGTAGGTGTTCCAG
>4.31|1519092|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ATCCAAGGAGATGCAACCCGCGGAATTCCTTCGAC
>4.32|1519159|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGAACGCTGAAGGAAGTATTACACTGCATCCAGG
>4.33|1519225|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
ACCTTCTGCTGCTGACGACAAACTGAAGAAGGTCGA
>4.34|1519293|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CGCGTGCGTGCGACCCTGCGCGGGCCGCGGATCA
>4.35|1519359|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GATACGAGATGCATATTTGGTTGTCGGCGTGCTG
>4.36|1519425|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CACTCATGTTCCCCGTGAAGTGCTCCGCATGTAC
>4.37|1519491|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TGAGAATGTGCCTCCAATCCAACCAGGACAACATC
>4.38|1519558|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CTCTTCAATGGTTACGAATTGATCATCATCTCC
>4.39|1519623|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
CCGATCACCGGCACTTCTTCCGCACCTAACGGGAC
>4.40|1519690|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
GGACTGTCCACGGTAACCTTTGGAGCCTCTGGCTG
>4.41|1519757|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
TTACCCACATCCAAATCAAAGCTCTTTTCAACT
>4.42|1519822|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AATCTATCCATGGTTCTGAAGGTCAACGAGCTGCT
>4.43|1519889|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT
AGATCTTCGCGACGCCGTCTGTAGCCCGTCTG
>4.44|1519953|36|NZ_CP009285|CRISPRCasFinder,CRT
CTAGATTGGCCTAAACTAGCTGATCTCACAAGAAAA
>4.45|1520021|33|NZ_CP009285|CRISPRCasFinder,CRT
ACATCGTTTATCACTGCCTACCAGTTGTCCAAT
>4.46|1520086|33|NZ_CP009285|CRISPRCasFinder,CRT
ATCAATCGCCTGTCCTCGGAATTGATCTCCGTG
>4.47|1520151|32|NZ_CP009285|CRISPRCasFinder,CRT
CATTTGGTCTGTGGTCTGCCGGTCGTAAATTG
>4.48|1520215|35|NZ_CP009285|CRISPRCasFinder
CCCATAAAGAAAGGAACAACCCAATGAATACCTTG

CRISPR arrays and Neighbor proteins around NZ_CP009285_4

CRISPR arrays

The CRISPR arrays of NZ_CP009285_4

>merge|NZ_CP009285|4|1517067-1520281|PILER-CR,CRISPRCasFinder,CRT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTCGGTAGTCAGTTTTTAAACAATAATGGCGGGGTTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTCCAGGAGACCGCGACCTAGATCGGCTGCCCGCGCCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATAGGTCATGAATCACGGGAACCGGCAGTACTACTAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATTGCCGCTTGTTGAATGGCTATGGTCTGCTTTGCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCGATCCCACCGGAGTTAGTAGATGCTTTTCCAGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATACATTATTTTGATAACATTGATACCGAAGAAAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATTGATAATTTAAAACGCCATGCGAAAGCATGTTGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCTACACACAGGGTGGGGATTTGTCTCAGACACATGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTGAAGAGGCGCATTCCGCTAATCCGGCCGATTTGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCGAAAGTCGTCGGAATACGAGGAACTACCGCCAGAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATAGAATCACTTTTGACTCAGGAATCACTAATTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTCCAGGTGAATGGTGCACAGCGGATGATGCTATTCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCATCCAGCGCTCTTAAATTGCTTTGCGGCGCTAGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATGTTAAAACGATGACCGCCTCTGACCGGATGTTTCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTGAGCTGCGAACCGTTACTTGGTCAGGTTGATCTAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATGTTCAGGGGGATATATGTTGGCTGTTGGAGATGAAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATAAACACCGGCGTCCGGAGCATCCCAGATTTGGTCCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCTACGGTTGGAGGTTTGCATTAAATGTTGGTTTTTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCCGTCAACAGTGTTACCAGCACTGTATCGGGGTTGGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATAACTTTTGCGCAGTGAATCAGCACCGCTTTCGGGTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTTTTTACCCTTGAACATTCCAGCAACCGAGTCCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATAGTTTCACCGCGGACTTTGCGCATTACAACGCGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATTCCGGTAGGCGTGTGCTTGGGCATCATGACCACGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATGATCTGCAGTTGCAGCGCGTCACCTGCGGTACCACGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATAGAAACTTGCTCTCATGGATCCAGCACTAAGCCTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATACCAAGAGTCAAACTATGAAATATCTGGAGAGAGCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATGAGGGTACACAAGAATGCGAAATGGTTCAGGTGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTTCGCTGTCTCGGCTGTATGTGGCTTTGATCTCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTTATAGGGAATGAGGTAAGCATGACCGAGGATAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATGTACCTGCCGACGCTGTGGGCGCTGTAGGTGTTCCAGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATATCCAAGGAGATGCAACCCGCGGAATTCCTTCGACGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCGAACGCTGAAGGAAGTATTACACTGCATCCAGGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATACCTTCTGCTGCTGACGACAAACTGAAGAAGGTCGAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCGCGTGCGTGCGACCCTGCGCGGGCCGCGGATCAGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATGATACGAGATGCATATTTGGTTGTCGGCGTGCTGGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCACTCATGTTCCCCGTGAAGTGCTCCGCATGTACGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATTGAGAATGTGCCTCCAATCCAACCAGGACAACATCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCTCTTCAATGGTTACGAATTGATCATCATCTCCGTCGCTCCTCGTGCAGGAGCGTGGATTGAAATCCGATCACCGGCACTTCTTCCGCACCTAACGGGACGTCGCTCCTCGTGTAGGAGCGTGGATTGAAATGGACTGTCCACGGTAACCTTTGGAGCCTCTGGCTGGTCGCTCCTCGTGTAGGAGCGTGGATTGAAATTTACCCACATCCAAATCAAAGCTCTTTTCAACTGTCGCTCCTCGTGTAGGAGCGTGGATTGAAATAATCTATCCATGGTTCTGAAGGTCAACGAGCTGCTGTCGCTCCTCGTGTAGGAGCGTGGATTGAAATAGATCTTCGCGACGCCGTCTGTAGCCCGTCTGGTTGCTCCTCGTGCAGGAGCGTGGATTGAAATCTAGATTGGCCTAAACTAGCTGATCTCACAAGAAAAGTCGCTCCTCGTGCAGGAGCATGGATTGAAATACATCGTTTATCACTGCCTACCAGTTGTCCAATGTCGCTCCCCGTGCAGAAGCGTGGATTGAAATATCAATCGCCTGTCCTCGGAATTGATCTCCGTGGTCGCTCCACGTGCAGGAGCGCGGATTGAAATCATTTGGTCTGTGGTCTGCCGGTCGTAAATTGGTCGCTCCTCATGTAGGAGCGTGGATTGAAATCCCATAAAGAAAGGAACAACCCAATGAATACCTTGGTCACTCCACGTGCAGGGGTGTTTGTTGAAAC

>NZ_CP009285|4|3|1517067-1519952|PILER-CR
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCGGTAGTCAGTTTTTAAACAATAATGGCGGGGTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGAGACCGCGACCTAGATCGGCTGCCCGCGCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGGTCATGAATCACGGGAACCGGCAGTACTACTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGCCGCTTGTTGAATGGCTATGGTCTGCTTTGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGATCCCACCGGAGTTAGTAGATGCTTTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACATTATTTTGATAACATTGATACCGAAGAAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGATAATTTAAAACGCCATGCGAAAGCATGTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACACACAGGGTGGGGATTTGTCTCAGACACATG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAAGAGGCGCATTCCGCTAATCCGGCCGATTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAAAGTCGTCGGAATACGAGGAACTACCGCCAGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATAGAATCACTTTTGACTCAGGAATCACTAATT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGTGAATGGTGCACAGCGGATGATGCTATTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CATCCAGCGCTCTTAAATTGCTTTGCGGCGCTAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTAAAACGATGACCGCCTCTGACCGGATGTTTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGCTGCGAACCGTTACTTGGTCAGGTTGATCTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTCAGGGGGATATATGTTGGCTGTTGGAGATGAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AAACACCGGCGTCCGGAGCATCCCAGATTTGGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACGGTTGGAGGTTTGCATTAAATGTTGGTTTTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGTCAACAGTGTTACCAGCACTGTATCGGGGTTGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AACTTTTGCGCAGTGAATCAGCACCGCTTTCGGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTTTTACCCTTGAACATTCCAGCAACCGAGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGTTTCACCGCGGACTTTGCGCATTACAACGCG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTCCGGTAGGCGTGTGCTTGGGCATCATGACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATCTGCAGTTGCAGCGCGTCACCTGCGGTACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGAAACTTGCTCTCATGGATCCAGCACTAAGCCT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCAAGAGTCAAACTATGAAATATCTGGAGAGAGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATGAGGGTACACAAGAATGCGAAATGGTTCAGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTCGCTGTCTCGGCTGTATGTGGCTTTGATCTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTATAGGGAATGAGGTAAGCATGACCGAGGATA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTACCTGCCGACGCTGTGGGCGCTGTAGGTGTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATCCAAGGAGATGCAACCCGCGGAATTCCTTCGAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAACGCTGAAGGAAGTATTACACTGCATCCAGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCTTCTGCTGCTGACGACAAACTGAAGAAGGTCGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGCGTGCGTGCGACCCTGCGCGGGCCGCGGATCA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATACGAGATGCATATTTGGTTGTCGGCGTGCTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CACTCATGTTCCCCGTGAAGTGCTCCGCATGTAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGAATGTGCCTCCAATCCAACCAGGACAACATC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTCTTCAATGGTTACGAATTGATCATCATCTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGATCACCGGCACTTCTTCCGCACCTAACGGGAC
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	GGACTGTCCACGGTAACCTTTGGAGCCTCTGGCTG
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	TTACCCACATCCAAATCAAAGCTCTTTTCAACT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AATCTATCCATGGTTCTGAAGGTCAACGAGCTGCT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AGATCTTCGCGACGCCGTCTGTAGCCCGTCTG
GTTGCTCCTCGTGCAGGAGCGTGGATTGAAAT

>NZ_CP009285|4|4|1517067-1520281|CRISPRCasFinder
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCGGTAGTCAGTTTTTAAACAATAATGGCGGGGTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGAGACCGCGACCTAGATCGGCTGCCCGCGCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGGTCATGAATCACGGGAACCGGCAGTACTACTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGCCGCTTGTTGAATGGCTATGGTCTGCTTTGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGATCCCACCGGAGTTAGTAGATGCTTTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACATTATTTTGATAACATTGATACCGAAGAAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGATAATTTAAAACGCCATGCGAAAGCATGTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACACACAGGGTGGGGATTTGTCTCAGACACATG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAAGAGGCGCATTCCGCTAATCCGGCCGATTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAAAGTCGTCGGAATACGAGGAACTACCGCCAGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATAGAATCACTTTTGACTCAGGAATCACTAATT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGTGAATGGTGCACAGCGGATGATGCTATTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CATCCAGCGCTCTTAAATTGCTTTGCGGCGCTAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTAAAACGATGACCGCCTCTGACCGGATGTTTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGCTGCGAACCGTTACTTGGTCAGGTTGATCTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTCAGGGGGATATATGTTGGCTGTTGGAGATGAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AAACACCGGCGTCCGGAGCATCCCAGATTTGGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACGGTTGGAGGTTTGCATTAAATGTTGGTTTTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGTCAACAGTGTTACCAGCACTGTATCGGGGTTGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AACTTTTGCGCAGTGAATCAGCACCGCTTTCGGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTTTTACCCTTGAACATTCCAGCAACCGAGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGTTTCACCGCGGACTTTGCGCATTACAACGCG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTCCGGTAGGCGTGTGCTTGGGCATCATGACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATCTGCAGTTGCAGCGCGTCACCTGCGGTACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGAAACTTGCTCTCATGGATCCAGCACTAAGCCT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCAAGAGTCAAACTATGAAATATCTGGAGAGAGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATGAGGGTACACAAGAATGCGAAATGGTTCAGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTCGCTGTCTCGGCTGTATGTGGCTTTGATCTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTATAGGGAATGAGGTAAGCATGACCGAGGATA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTACCTGCCGACGCTGTGGGCGCTGTAGGTGTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATCCAAGGAGATGCAACCCGCGGAATTCCTTCGAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAACGCTGAAGGAAGTATTACACTGCATCCAGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCTTCTGCTGCTGACGACAAACTGAAGAAGGTCGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGCGTGCGTGCGACCCTGCGCGGGCCGCGGATCA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATACGAGATGCATATTTGGTTGTCGGCGTGCTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CACTCATGTTCCCCGTGAAGTGCTCCGCATGTAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGAATGTGCCTCCAATCCAACCAGGACAACATC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTCTTCAATGGTTACGAATTGATCATCATCTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGATCACCGGCACTTCTTCCGCACCTAACGGGAC
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	GGACTGTCCACGGTAACCTTTGGAGCCTCTGGCTG
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	TTACCCACATCCAAATCAAAGCTCTTTTCAACT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AATCTATCCATGGTTCTGAAGGTCAACGAGCTGCT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AGATCTTCGCGACGCCGTCTGTAGCCCGTCTG
GTTGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTAGATTGGCCTAAACTAGCTGATCTCACAAGAAAA
GTCGCTCCTCGTGCAGGAGCATGGATTGAAAT	ACATCGTTTATCACTGCCTACCAGTTGTCCAAT
GTCGCTCCCCGTGCAGAAGCGTGGATTGAAAT	ATCAATCGCCTGTCCTCGGAATTGATCTCCGTG
GTCGCTCCACGTGCAGGAGCGCGGATTGAAAT	CATTTGGTCTGTGGTCTGCCGGTCGTAAATTG
GTCGCTCCTCATGTAGGAGCGTGGATTGAAAT	CCCATAAAGAAAGGAACAACCCAATGAATACCTTG
GTCACTCCACGTGCAGGGGTGTTTGTTGAAAC

>NZ_CP009285|4|3|1517067-1520214|CRT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCGGTAGTCAGTTTTTAAACAATAATGGCGGGGTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGAGACCGCGACCTAGATCGGCTGCCCGCGCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGGTCATGAATCACGGGAACCGGCAGTACTACTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGCCGCTTGTTGAATGGCTATGGTCTGCTTTGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGATCCCACCGGAGTTAGTAGATGCTTTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACATTATTTTGATAACATTGATACCGAAGAAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTGATAATTTAAAACGCCATGCGAAAGCATGTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACACACAGGGTGGGGATTTGTCTCAGACACATG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAAGAGGCGCATTCCGCTAATCCGGCCGATTTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAAAGTCGTCGGAATACGAGGAACTACCGCCAGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATAGAATCACTTTTGACTCAGGAATCACTAATT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TCCAGGTGAATGGTGCACAGCGGATGATGCTATTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CATCCAGCGCTCTTAAATTGCTTTGCGGCGCTAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTAAAACGATGACCGCCTCTGACCGGATGTTTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGCTGCGAACCGTTACTTGGTCAGGTTGATCTA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTTCAGGGGGATATATGTTGGCTGTTGGAGATGAA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AAACACCGGCGTCCGGAGCATCCCAGATTTGGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTACGGTTGGAGGTTTGCATTAAATGTTGGTTTTT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGTCAACAGTGTTACCAGCACTGTATCGGGGTTGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AACTTTTGCGCAGTGAATCAGCACCGCTTTCGGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTTTTACCCTTGAACATTCCAGCAACCGAGTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGTTTCACCGCGGACTTTGCGCATTACAACGCG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATTCCGGTAGGCGTGTGCTTGGGCATCATGACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATCTGCAGTTGCAGCGCGTCACCTGCGGTACCAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	AGAAACTTGCTCTCATGGATCCAGCACTAAGCCT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCAAGAGTCAAACTATGAAATATCTGGAGAGAGC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATGAGGGTACACAAGAATGCGAAATGGTTCAGGT
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTCGCTGTCTCGGCTGTATGTGGCTTTGATCTC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TTATAGGGAATGAGGTAAGCATGACCGAGGATA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GTACCTGCCGACGCTGTGGGCGCTGTAGGTGTTCCAG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ATCCAAGGAGATGCAACCCGCGGAATTCCTTCGAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGAACGCTGAAGGAAGTATTACACTGCATCCAGG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	ACCTTCTGCTGCTGACGACAAACTGAAGAAGGTCGA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CGCGTGCGTGCGACCCTGCGCGGGCCGCGGATCA
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	GATACGAGATGCATATTTGGTTGTCGGCGTGCTG
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CACTCATGTTCCCCGTGAAGTGCTCCGCATGTAC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	TGAGAATGTGCCTCCAATCCAACCAGGACAACATC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTCTTCAATGGTTACGAATTGATCATCATCTCC
GTCGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CCGATCACCGGCACTTCTTCCGCACCTAACGGGAC
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	GGACTGTCCACGGTAACCTTTGGAGCCTCTGGCTG
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	TTACCCACATCCAAATCAAAGCTCTTTTCAACT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AATCTATCCATGGTTCTGAAGGTCAACGAGCTGCT
GTCGCTCCTCGTGTAGGAGCGTGGATTGAAAT	AGATCTTCGCGACGCCGTCTGTAGCCCGTCTG
GTTGCTCCTCGTGCAGGAGCGTGGATTGAAAT	CTAGATTGGCCTAAACTAGCTGATCTCACAAGAAAA
GTCGCTCCTCGTGCAGGAGCATGGATTGAAAT	ACATCGTTTATCACTGCCTACCAGTTGTCCAAT
GTCGCTCCCCGTGCAGAAGCGTGGATTGAAAT	ATCAATCGCCTGTCCTCGGAATTGATCTCCGTG
GTCGCTCCACGTGCAGGAGCGCGGATTGAAAT	CATTTGGTCTGTGGTCTGCCGGTCGTAAATTG
GTCGCTCCTCATGTAGGAGCGTGGATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210978.1|1523556_1523916_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|379188
NZ_CP009285.1|WP_167549522.1|1523019_1523187_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|226175
NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|271156
NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein	unknown	unknown	gnl|CDD|235290
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA	unknown	unknown	gnl|CDD|380221
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|273040
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	1.4e-147	485.9	0.3
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	1.5e-127	419.4	0.3
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1.4e-59	196.0	0.0
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	2.4e-85	282.0	9.7
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	2.4e-33	110.5	1.3
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	2.8e-31	102.3	0.7
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	6.6e-159	524.6	1.8

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein	gnl|CDD|271156	cd14490, CBM6-CBM35-CBM36_like_1, uncharacterized members of the carbohydrate binding module 6 (CBM6) and CBM35_like superfamily. Carbohydrate binding module family 6 (CBM6, family 6 CBM), also known as cellulose binding domain family VI (CBD VI), and related CBMs (CBM35 and CBM36). These are non-catalytic carbohydrate binding domains found in a range of enzymes that display activities against a diverse range of carbohydrate targets, including mannan, xylan, beta-glucans, cellulose, agarose, and arabinans. These domains facilitate the strong binding of the appended catalytic modules to their dedicated, insoluble substrates. Many of these CBMs are associated with glycoside hydrolase (GH) domains. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold. CBM36s are calcium-dependent xylan binding domains. CBM35s display conserved specificity through extensive sequence similarity, but divergent function through their appended catalytic modules.	1.36045e-66
NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.50482e-92
NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	8.725e-08
NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	2.74607e-25
NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	1.81468e-15
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	5.27896e-19
NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA	gnl|CDD|380221	NF033225, spore_CmpA, cortex morphogenetic protein CmpA. Members of this family are CmpA (cortex morphogenetic protein A), a small protein (37 amino acids) involved in endospore formation and frequently missed during genome annotation.	4.44095e-17
NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein	gnl|CDD|235290	PRK04351, PRK04351, SprT family protein.	1.54725e-76
NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|226175	COG3649, COG3649, CRISPR system related protein [Defense mechanisms].	1.02785e-134
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	3.08255e-54
NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	2.84039e-75
NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	3.26425e-07
NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4	gnl|CDD|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	2.76046e-30
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.79564e-34
NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	7.7654e-167

Protein sequences

>NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2
MLVLITYDVSTTSSAGQSRLRRVAKICQNYGQRVQNSVFECIVDAAQFTELKLKLKDIINLKEDSLRFYQLGNNYKNKVEHVGIKESLDLEGPLIL
>NZ_CP009285.1|WP_042210973.1|1515567_1516599_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLQNTLYITQPDVYLSLDGDNVVLLKEQEKLGRVPLHNLESIVAFGYTGASPALMGYCADNNVSLLFLTMNGRFLARVTGESRGNVILRKKQYALSEDETKSARIARNFIIGKIYNHKWILERTTRDYPLRVNVEQFKEASQQLSALILEVRNCEQLDRLRGFEGQAAITYNKLFDSMILQQKEDFQFHLRSRRPPLDNVNAMLSFSYTLLAHDTASALEAVGLDSYVGFLHRDRPGRVSLALDLMEELRGVMADKFVLTQINKKLVSKEDFVKKENGAVIMTDEARKRFLTAWQNRKQEKITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_CP009285.1|WP_042210972.1|1514911_1515571_+|CRISPR-associated-protein-Cas4
MAYSDDDDALMLSGIQHFHFCKRQWALIHIEQQWAEDFRTIEGQHLHRNADQPFTREKRGDKLVVRAMPVKSRQLGITGICDVVEFIRDNSGVEINGAEGKYVAYPVEYKRGKPKLEDIDVLQLTAQAMCLEEMLLCDVRTGYIFYNEIKHRIEVPLTDELKLKVGSILEEMQDYYRRGYTPKVRTGAFCESCSLQHICLPKLMNKQTVKSYVEGKIRE
>NZ_CP009285.1|WP_042210971.1|1514058_1514922_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTTLDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDAGESIFVQSNDRKNDSFGSLRERADANPELDKILKAKTSSNEEFARIACQEWIDVRSFGQVFAFKADSKGSGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDYGLYVFYGSINTQLAEKTGFTNEDADKIKEALITLFANDVSSARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLDVRALKDEPKSIEDYSIEVYQLEGLQPEVMNGL
>NZ_CP009285.1|WP_042210970.1|1512111_1514055_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYKANVDRVGEIETKHNDREYTLLPVSHTTQNAHITVEITEAGEFHSAIVNDKSDISTLIPCTEESSSRAGSKIAPYPLHDKLSYVAGDFVAYGGQIKKEEPFAAYIKQLEEWANSPYASPKVKSIYTYLSKRRLIQDLVAWRVIFLDANDKLIDKWDKKYEALHGEKPPIFTLVAGEQESAFVRFNVRKQNDHTMVWKDSEMFNSFVQHYSSLLGKEDFCYVTGEILPSTDRHANKIRNAGDKAKLISANDTSGFTFRGRFAQSSDAASISYEVSQKAHNALKWLINRQGKIIDQRVFLVWGNDDLDIPDPNADTFTLKLELEPEMEPELKPVAADVKISHTYKEYAREVAKALDGYRNRLASRSKSNVNILILDSATTGRLAVLYYRNMEKNLYVDQLIKWHSTCAWLHKYRKNEQGETATFYGAPSTKDVAFAAYGPKANEKVVKGMMERVLPCIVDGHKIPQDIVRSAFQRASNPVALESWEWEKTLSITCALINTREVYNVALDTENDDRSYLFGRLLAIADVLERRALDSDERRSTNAIRYMNSFSRYPARTWSTIQSCLLPHQARLGTRVRYYSNLIDEVASKIKIEEFDNKALTGKYLLGFYSQRHELNYGKAKSGDSNPTIPTSNHEER
>NZ_CP009285.1|WP_042210969.1|1511392_1512115_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGVVESIYWKPTLIIVVDEVRVMNAIRMESKGIRPMEYGGGNTLANYTYLKEPHYEVRAHFVFNENRPDLAHDRNEHKHHNILKRSLEAGGRRDIFLGARECQAYVEPCVFGEAPGYYDTYDGEIHFGNMVHGINYPDETGRDQMEVRLWNPVMKNGYIKFDKPEDCTKVRRIADMQPKLFDHHNVQSVDELFEEIEAGGQS
>NZ_CP009285.1|WP_042210968.1|1511058_1511277_+|hypothetical-protein
MNNSTFSLVEDYPDYYKKKPVSKLQGFFSRSPELPSKQELSVESLLKKQRLRIGELQQENEILRKAMHLLTK
>NZ_CP009285.1|WP_042219011.1|1508341_1510789_+|CRISPR-associated-helicase/endonuclease-Cas3
MDYIAHIRESDGRIQTVTEHLLEVRALAEAFGEKLGVRHIAGLAGVLHDLGKYTEEFREYILAAVNNPDAPPRRGSVDHSTAGGKLLFDWFHPSSPEYANERVSQTKAILAEIVGNAIISHHSYLQDFLNPDLESSYLKRVRDKHLEEFSSLTLKMFFEQVINEQEFRLYVDQAELELIAFLKKEPKVTLEHRAMLLSKFIFSALIDADRTNTRSFEANKNDDEVDHKVLFEQYYDRLITRINSFQTHKNADSEINRLRREMSEQCDAFANNGSGIYTLSIPTGGGKTLASVRYALKHARIFNKQRVIYVIPFTTIIEQNAAEVRKILMDDEHILEHHSNVVEAETEDDEQEDGKAVIGQKLKLAKDNWDAPVIFTTMVQFLNVFYADGSRNIRRLHNLSNAVIIFDEVQKVPVSCISLFNYAVNFLKTYANSSIVLCTATQPELDYVRYKLQLSPEAEMISSLDDVVKAFKRVDIIDRATGEQFNTDKLADFVLDKIQDVLSVLVILNTRSVVKALYNKLQEQDLSIPIYHLSTSMCAAHRKEILVEVKRLLEAKLPVICISTQLIEAGVDVSFKCVIRSLAGLDSIAQAAGRCNRHGEDEIQQVYVIDHSEEDLKKLKEIRVGKDKTRKILVDFCRDPVRLGGHLLSVQAMKQYFQEFYTELASSLNYNIPKLEKEMTGLLSADRVSNSFHSEYRSEHNASVPLYLHNSYKTAAEHFHVIDNHTTSVIVPYERGKEIIADLNGQHSIQDLSKLLREAQQFTINLFNFEKDTLGKINGIVPYLDGKVFALKEGTYSSEYGLDLKGESVMEVSLY
>NZ_CP009285.1|WP_052429357.1|1504689_1505331_+|hypothetical-protein
MSKRRPRKLNVQAILDIIKKNLVWPELKGLPDAIHYYHLTDALGRKWQTIGCHVTDAIKVFKMGEYPPWTLIIESAPYDPHITVRELIAMLNCEDNALVNDMQIILNTTVRCNQFINVIVNVNYYSIFTVLYDLKNDYLLNDPIPISDFEAMYNINPIEALSRFYLENVDTLDYWVWVQAGGSAELAVNFRKANPTLTLIEAIEKLERMRDIT
>NZ_CP009285.1|WP_039301959.1|1504301_1504535_-|helix-turn-helix-transcriptional-regulator
MEFKDYTLYCKLDTILKAHDISVLKLSKEIGHRRTTIMELMHNTNMEKKKISAELIMKLCLYFEVTPNDLFEIRRKE
>NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein
MGPSDTSAQRQAKWIKRFLRTYWLVIALHFAAQLWAFLFLSYPMGPHEFYYDVLLYPTLLMSAVVGLTQFVDAIAPKYSFVLLFVSGTIIAMMIIHLNMDIRIIGALMLLPIFASAIFFRLDLTLFTSALQAAAFFILYRWDYWFKYYLNDFDLIAVPLFLLVGTLVAGIIIINGRELASDLEATLTAKQNLMIENAVIRKLSTTDALTGLYNHISFHEFYEKALEYGNQGAPFHLALIDIDNFKRINDKYGHRTGDAVLARVAKVIKENISPADIASRYGGEEFAILFFEKSYEEAYELADRVRQQLSETLHEELENTAVTVSIGLKSYSEGATKEQLFEEVDELLYTAKKSGKNTTLTPLQQTRHLQSV
>NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein
MLWEDFINSYWRNWRTGDRSTDRDRLDEPEWLTRWLEQQKLPAAGPILPVELERLKQLRGLLWDEVQRLVQGQPTESALLEQLNEYMSNGPVMRQVVWSPGGEAGISLLPQRADWEQIMAEIAASFAEALLEKESSRFRICGNPDCLWVYYDDTRNRSKRYCDDKLCGNLMKVRRFRARRKAAEDEGNLPD
>NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein
MQNKISDVLVENWDYVMDVEDWQPPLKDALEGVTSEQASWKPEGAAGNSIWETVNHLTYYKERLLRKLKGLEKLPDLESNDATFTVTESGEEAWSQAVAKLKSVHASLREIIVALEEGAYEWGGSGHAPGEEVMSLILHDSYHTGQIVLVRKLQGSWPGQRSFD
>NZ_CP009285.1|WP_167549522.1|1523019_1523187_+|hypothetical-protein
MEPNTKDRSIEVERTEVHKKSDSSLVASTFIKYAAYIIIIFGLLFFLVKYVFPMF
>NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA
MPQWLCQQLMKAYFKKDRRQIKLLNECWFFYRNSAETREFITKDV
>NZ_CP009285.1|WP_042210978.1|1523556_1523916_-|hypothetical-protein
MPKMRYVILQQDQELQFVEMPEEYAYQLSALNLRLNKEIDKLTAENVPGLPRAIAECDSLELLREEHHLESGLAYINRLESAFASIQETEYPLISLLTEIRALQAQLEQWYEEEEESVH
>NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein
MSNEELQLWIEQVSMNSFGVPFRHTASFNSRLTTTGGRYFTKSHNIEINPQQLAIHGREETEKIIKHELCHYHLHLAKRGYMHRDDDFKTLLARVGGSRYCQTLPGAKARKPQPYRYKLVCVACATEYLRKRKADPKRYRCGKCSGKLKLVTLEAGAGPAT
>NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein
MNNKIEQPRIPEPELLLPQQIHSLASKDEFSRCLISGALIEYQDAARVSFDKVIFKNVTITESSLHGIELTDVIFDHCDLSNVDFSEAFMHRTEFRDCRLIGTDFTRARFQNVSVTGCIGEFAVFRFANFKAASFERSSLISADYYQSALNGLYFSECNLDQATLAGCKLKDIDLSDCEFTGLVVDLQDLDGCVISAEQAASFAGLLGLVIKY
>NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein
MKRFRSVIAGLLALLLIFPNLGLPGAGNSVYADGLGGTGAAQIPAGTVLIKNKWKNNFLYETSEGVVRYGMTNPADTSSHWNVVTEGGLSRIQNVKTGHFITLEGNTGKEDSLKAAAAPGGGSTADQWLIDTSNRAGYMVIRSATAPEGKLVIHEENQLGYAQVSADINITFESPQWAFVSLNAAPVRIESVMRPGNVMFENEGKVQHGAEPLSNEAAQWFLEPGTDSGTLLIRNRATGHYIKQNEDPNYGVFSAEIDPAKANLSEWIQESAPGTPEAGLVTFRNQGLTDGGNALWLSPQYDGDSDVRSNNWPGWGGNPSAQWRIVTVSELQPVRITTYTDAQVATDFLYEAAGGELQHGVIAPDAADESKYLWFVEDYDGHKRIRNAATGHYLNYADGTAAAVTMNMSLPSDQWNFNESDDYDDYQTIENVGATGNYLSLLGGGHAGAGSDASSLSAQWQLLDPNLHADGSLHYYRIQNTWQSFYWYESSDGVLKYGNMQEDGSDQWLIEKYNGRKLFQNKKTGHYMNVAQMPDGHISVTPLDGKDNVDPAYIWTGRNTGDSTYVIASVLDKEPNKRPLKYISLQNLTKYAEYGVINPDWGSPKWKFVPVTEKKHDLFRFKLDGVNGADQYLKDDAVPAPVLKVTLPVNDGTVTADVYDPQDQAGGDLEDIAKKAAKEEEALLALDAGDTATAGAGGGAAADPTVGQATYGELIPGDDSFVWQLIDIPGSNGAVKLKNRGTGRYISLESLAAVIEQEEPPGPVRTEQTVYDVWASIRWIVDIQESGRTTFKSAWAGHYLYGAADDNGYPVIRISKAADAAVRDSAQFTAEPVYEPVPPLPAAPVRFKNAGTGDYLYENEHGVVLYGQPASDNGYSHWNIVTDAGQQFIVNRATGHYITLNSDYSFLESTGGDPADTGASAWAVSLAADAKHYTIRSLYGEYNDEYINLQNKTGYAERALLLDTESSLQWTLEAAPQEFNLPEGEAGNTDTATPVQNDTNIITIAPQGMDGTLVAEKDGKLVYADASGGPAQAQWLVQDFNGRNRVMNVQTGHYLARDQEGAIVLTDSGDKVDSQWSIQDKLGYRLLLSADKQSALAHGEAGVQLGAAGAQAALWSFVPVAQDAVYAGQEAFRGDGVLRFAVNADVAGEYDVVLRYRNTAAAAAKLETRVNGLKQGEVSLPASASVWQTAELTLELRTGINTISFSGAEASWSGITIDSLTVKDSVNKSYRGATLPYISYEAEDAVTNGTLVTPSRKYRSLASEASGREAVILKNTGEYVEFTLAKPANSIVLRYSIPDSPDGAGAEETLSLFVNGELQELNLTSKYAWEYGSYPWSNDPRQGSGHRFYDEIHALIGDAPAGAVIRLEKGAEDTAASYVIDLADMEQVAPALAQPEGFLSVTDFGAVAGDDGDDTAAFKAALAAAAAQDAGVWFPAGSFNVGNGLLDLDDAEIRGAGMWYTTLNGAKFYGHGGEIGVYDLLIEGGINVRDDEAVTNAFHGAFGQGSVIQNVWIEHTKAGLWLTQPKGEKARTNGLYMAGLRIRNLMADGINFAVGTGNSMMEQSDIRYPGDDGIAMWSFTDAGLNDVNGSERTPSFNNTARFNNVSLPWLADNIVVFGGKDNKIQDNIVKDTVTNGAGIAVSTRFSAEPFQGTTVVERNTLLRTGSYDSGYSVNLGAIWLYAGENNINSNVLIRNNIALDSTYSGLIVHGNLNMEGVTLTDNVIDGAGTNGVEITKEMRGGLLADNLIIRGERMNQVANSSSAFTVLEKNQGIASSIKPFSIKLGDGQTGPVVLKEGTSSKLQVLDQKGTDITAQADIRIANGSLATMEDGKLQAIAKGNTTFSVSALGSTRVYDLVIWAADPVDPVDPVDPVDPVDPVDPVDPGTPTPTPSLEPTPSPTAAPTPTSTPAPDPNPQPTSASTPAPVIVPAANNDAQLKSVAAGQKVIEVAANADGTARFSGAALRAAAAASPDAVLVVRSGDASYRLPLSLADSVLKGAKLPDGTLEFKLAPQTGAELAGLLAAAGKQNYKVKGTPAGFTLNVTDGKTSVPAGSFGTVYVERTFTINEVMDAKTAVALVYNAKDGTFRYVPALFESGAGVTRVTVKSSLAGGVIAVAANPVSFGDISAHWAKDEISLLASRLIVNGQSAGVFAPQRTVSRAEFASMLVRSLGLQPDTLPAAAATFSDVPASSWYAADAEAAVLLGLVQGYADGSFRPDAPITREQMAVMAARAWKLLHANAAINEAGSPAAPSAPGSFNDAASISGWAKEAVDTLTARSIMNGRSGGSFAPGSNTSRAEAAVILTRLLRAGKLLNE
>NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator
MSPYLIDDTDYRILQLLIEDSTLSHKDIGAEVHLTGQAVGARIRRMRELEIIEGYTIRWNPLRIGQNMHAFITVFLSTNAAHLPFQNFAKNHSSVAELYRISGEGCYWMRVRTVNQEALAAFLDELLGYGNYRVNLDMGQIK

Crispr_ID: NZ_CP009285_5

• CRISPR_ID: NZ_CP009285_5
• CRISPR_location: 1532884-1533062
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 3 spacers
• Cas_protein_info: cas2

Consensus repeat of NZ_CP009285_5

Consensus_repeat	Method
AAATCTTGCAGAAAATACAACAAT	CRISPRCasFinder

spacers of NZ_CP009285_5

>5.1|1532908|28|NZ_CP009285|CRISPRCasFinder
GTGGGGCTCAAAACTCCCCATTTGCTAG
>5.2|1532960|28|NZ_CP009285|CRISPRCasFinder
TTGAGGCTCGAAGCTGCTAACCCGCCAG
>5.3|1533012|27|NZ_CP009285|CRISPRCasFinder
GTGGGTTCACAAGCGCCAAACCGCCCA

CRISPR arrays and Neighbor proteins around NZ_CP009285_5

CRISPR arrays

The CRISPR arrays of NZ_CP009285_5

>merge|NZ_CP009285|5|1532884-1533062|CRISPRCasFinder
AAATCTTGCAGAAAATACAACAATGTGGGGCTCAAAACTCCCCATTTGCTAGAAATCCTGCAGAAAATACAACAATTTGAGGCTCGAAGCTGCTAACCCGCCAGAATTCTTGCAAAAAGTACAACAATGTGGGTTCACAAGCGCCAAACCGCCCAAAATCTTGCAAAAAATACAACAAT

>NZ_CP009285|5|5|1532884-1533062|CRISPRCasFinder
AAATCTTGCAGAAAATACAACAAT	GTGGGGCTCAAAACTCCCCATTTGCTAG
AAATCCTGCAGAAAATACAACAAT	TTGAGGCTCGAAGCTGCTAACCCGCCAG
AATTCTTGCAAAAAGTACAACAAT	GTGGGTTCACAAGCGCCAAACCGCCCA
AAATCTTGCAAAAAATACAACAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|271156
NZ_CP009285.1|WP_042219017.1|1538659_1539565_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|223633
NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA	unknown	unknown	gnl|CDD|380221
NZ_CP009285.1|WP_042210986.1|1541301_1542003_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213191
NZ_CP009285.1|WP_042210978.1|1523556_1523916_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_CP009285.1|WP_042210983.1|1536189_1537107_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP009285.1|WP_042210985.1|1540514_1541297_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223488
NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein	unknown	unknown	gnl|CDD|235290
NZ_CP009285.1|WP_167549522.1|1523019_1523187_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_CP009285.1|WP_174479807.1|1539577_1540546_+|branched-chain-amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|119323
NZ_CP009285.1|WP_042210982.1|1535148_1536153_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP009285.1|WP_042210984.1|1537125_1538208_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_CP009285.1|WP_042210987.1|1542081_1543278_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|380570
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP009285.1|WP_042210981.1|1533790_1534543_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|225130

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	2.8e-31	102.3	0.7

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein	gnl|CDD|271156	cd14490, CBM6-CBM35-CBM36_like_1, uncharacterized members of the carbohydrate binding module 6 (CBM6) and CBM35_like superfamily. Carbohydrate binding module family 6 (CBM6, family 6 CBM), also known as cellulose binding domain family VI (CBD VI), and related CBMs (CBM35 and CBM36). These are non-catalytic carbohydrate binding domains found in a range of enzymes that display activities against a diverse range of carbohydrate targets, including mannan, xylan, beta-glucans, cellulose, agarose, and arabinans. These domains facilitate the strong binding of the appended catalytic modules to their dedicated, insoluble substrates. Many of these CBMs are associated with glycoside hydrolase (GH) domains. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold. CBM36s are calcium-dependent xylan binding domains. CBM35s display conserved specificity through extensive sequence similarity, but divergent function through their appended catalytic modules.	1.36045e-66
NZ_CP009285.1|WP_042219017.1|1538659_1539565_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|223633	COG0559, LivH, Branched-chain amino acid ABC-type transport system, permease components [Amino acid transport and metabolism].	1.5654e-82
NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA	gnl|CDD|380221	NF033225, spore_CmpA, cortex morphogenetic protein CmpA. Members of this family are CmpA (cortex morphogenetic protein A), a small protein (37 amino acids) involved in endospore formation and frequently missed during genome annotation.	4.44095e-17
NZ_CP009285.1|WP_042210986.1|1541301_1542003_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213191	cd03224, ABC_TM1139_LivF_branched, ATP-binding cassette domain of branched-chain amino acid transporter. LivF (TM1139) is part of the LIV-I bacterial ABC-type two-component transport system that imports neutral, branched-chain amino acids. The E. coli branched-chain amino acid transporter comprises a heterodimer of ABC transporters (LivF and LivG), a heterodimer of six-helix TM domains (LivM and LivH), and one of two alternative soluble periplasmic substrate binding proteins (LivK or LivJ). ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules.	6.69511e-125
NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	2.74607e-25
NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	1.81468e-15
NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	5.27896e-19
NZ_CP009285.1|WP_042210983.1|1536189_1537107_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.40952e-19
NZ_CP009285.1|WP_042210985.1|1540514_1541297_+|ABC-transporter-ATP-binding-protein	gnl|CDD|223488	COG0411, LivG, ABC-type branched-chain amino acid transport systems, ATPase component [Amino acid transport and metabolism].	9.99852e-131
NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein	gnl|CDD|235290	PRK04351, PRK04351, SprT family protein.	1.54725e-76
NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	3.08255e-54
NZ_CP009285.1|WP_174479807.1|1539577_1540546_+|branched-chain-amino-acid-ABC-transporter-permease	gnl|CDD|119323	cd06581, TM_PBP1_LivM_like, Transmembrane subunit (TM) of Escherichia coli LivM and related proteins. LivM is one of two TMs of the E. coli LIV-1/LS transporter, a Periplasmic Binding Protein (PBP)-dependent ATP-Binding Cassette (ABC) transporter involved in the uptake of branched-chain amino acids (AAs). These types of transporters generally bind type 1 PBPs. PBP-dependent ABC transporters consist of a PBP, two TMs, and two cytoplasmic ABCs, and are mainly involved in importing solutes from the environment. The solute is captured by the PBP, which delivers it to a gated translocation pathway formed by the two TMs. The two ABCs bind and hydrolyze ATP and drive the transport reaction. E. coli LivM forms a heterodimer with another TM, LivH, to generate the transmembrane pore. LivH is not included in this subgroup. The LIV-1/LS transporter is comprised of two TMs (LivM and LivH), two ABCs (LivG and LivF), and one of two alternative PBPs, LivJ (LIV-BP) or LivK (LS-BP). In addition to transporting branched-chain AAs including leucine, isoleucine and valine, the E. coli LIV-1/LS transporter is involved in the uptake of the aromatic AA, phenylalanine.	1.0522e-84
NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.79564e-34
NZ_CP009285.1|WP_042210984.1|1537125_1538208_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	9.53673e-83
NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	3.26425e-07
NZ_CP009285.1|WP_042210987.1|1542081_1543278_+|ABC-transporter-substrate-binding-protein	gnl|CDD|380570	cd06347, PBP1_ABC_LivK_ligand_binding-like, type 1 periplasmic ligand-binding domain of uncharacterized ABC (Atpase Binding Cassette)-type active transport systems predicted to be involved in uptake of amino acids, peptides, or inorganic ions. This subgroup includes the type 1 periplasmic ligand-binding domain of uncharacterized ABC (Atpase Binding Cassette)-type active transport systems that are predicted to be involved in uptake of amino acids, peptides, or inorganic ions. This subgroup has high sequence similarity to members of the family of hydrophobic amino acid transporters (HAAT), such as leucine-isoleucine-valine binding protein (LIVBP); however, its ligand specificity has not been determined experimentally.	7.78434e-160
NZ_CP009285.1|WP_042210982.1|1535148_1536153_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	2.73563e-55
NZ_CP009285.1|WP_042210981.1|1533790_1534543_+|MBL-fold-metallo-hydrolase	gnl|CDD|225130	COG2220, COG2220, Predicted Zn-dependent hydrolases of the beta-lactamase fold [General function prediction only].	1.9486e-17

Protein sequences

>NZ_CP009285.1|WP_052429358.1|1525389_1532340_+|S-layer-homology-domain-containing-protein
MKRFRSVIAGLLALLLIFPNLGLPGAGNSVYADGLGGTGAAQIPAGTVLIKNKWKNNFLYETSEGVVRYGMTNPADTSSHWNVVTEGGLSRIQNVKTGHFITLEGNTGKEDSLKAAAAPGGGSTADQWLIDTSNRAGYMVIRSATAPEGKLVIHEENQLGYAQVSADINITFESPQWAFVSLNAAPVRIESVMRPGNVMFENEGKVQHGAEPLSNEAAQWFLEPGTDSGTLLIRNRATGHYIKQNEDPNYGVFSAEIDPAKANLSEWIQESAPGTPEAGLVTFRNQGLTDGGNALWLSPQYDGDSDVRSNNWPGWGGNPSAQWRIVTVSELQPVRITTYTDAQVATDFLYEAAGGELQHGVIAPDAADESKYLWFVEDYDGHKRIRNAATGHYLNYADGTAAAVTMNMSLPSDQWNFNESDDYDDYQTIENVGATGNYLSLLGGGHAGAGSDASSLSAQWQLLDPNLHADGSLHYYRIQNTWQSFYWYESSDGVLKYGNMQEDGSDQWLIEKYNGRKLFQNKKTGHYMNVAQMPDGHISVTPLDGKDNVDPAYIWTGRNTGDSTYVIASVLDKEPNKRPLKYISLQNLTKYAEYGVINPDWGSPKWKFVPVTEKKHDLFRFKLDGVNGADQYLKDDAVPAPVLKVTLPVNDGTVTADVYDPQDQAGGDLEDIAKKAAKEEEALLALDAGDTATAGAGGGAAADPTVGQATYGELIPGDDSFVWQLIDIPGSNGAVKLKNRGTGRYISLESLAAVIEQEEPPGPVRTEQTVYDVWASIRWIVDIQESGRTTFKSAWAGHYLYGAADDNGYPVIRISKAADAAVRDSAQFTAEPVYEPVPPLPAAPVRFKNAGTGDYLYENEHGVVLYGQPASDNGYSHWNIVTDAGQQFIVNRATGHYITLNSDYSFLESTGGDPADTGASAWAVSLAADAKHYTIRSLYGEYNDEYINLQNKTGYAERALLLDTESSLQWTLEAAPQEFNLPEGEAGNTDTATPVQNDTNIITIAPQGMDGTLVAEKDGKLVYADASGGPAQAQWLVQDFNGRNRVMNVQTGHYLARDQEGAIVLTDSGDKVDSQWSIQDKLGYRLLLSADKQSALAHGEAGVQLGAAGAQAALWSFVPVAQDAVYAGQEAFRGDGVLRFAVNADVAGEYDVVLRYRNTAAAAAKLETRVNGLKQGEVSLPASASVWQTAELTLELRTGINTISFSGAEASWSGITIDSLTVKDSVNKSYRGATLPYISYEAEDAVTNGTLVTPSRKYRSLASEASGREAVILKNTGEYVEFTLAKPANSIVLRYSIPDSPDGAGAEETLSLFVNGELQELNLTSKYAWEYGSYPWSNDPRQGSGHRFYDEIHALIGDAPAGAVIRLEKGAEDTAASYVIDLADMEQVAPALAQPEGFLSVTDFGAVAGDDGDDTAAFKAALAAAAAQDAGVWFPAGSFNVGNGLLDLDDAEIRGAGMWYTTLNGAKFYGHGGEIGVYDLLIEGGINVRDDEAVTNAFHGAFGQGSVIQNVWIEHTKAGLWLTQPKGEKARTNGLYMAGLRIRNLMADGINFAVGTGNSMMEQSDIRYPGDDGIAMWSFTDAGLNDVNGSERTPSFNNTARFNNVSLPWLADNIVVFGGKDNKIQDNIVKDTVTNGAGIAVSTRFSAEPFQGTTVVERNTLLRTGSYDSGYSVNLGAIWLYAGENNINSNVLIRNNIALDSTYSGLIVHGNLNMEGVTLTDNVIDGAGTNGVEITKEMRGGLLADNLIIRGERMNQVANSSSAFTVLEKNQGIASSIKPFSIKLGDGQTGPVVLKEGTSSKLQVLDQKGTDITAQADIRIANGSLATMEDGKLQAIAKGNTTFSVSALGSTRVYDLVIWAADPVDPVDPVDPVDPVDPVDPVDPGTPTPTPSLEPTPSPTAAPTPTSTPAPDPNPQPTSASTPAPVIVPAANNDAQLKSVAAGQKVIEVAANADGTARFSGAALRAAAAASPDAVLVVRSGDASYRLPLSLADSVLKGAKLPDGTLEFKLAPQTGAELAGLLAAAGKQNYKVKGTPAGFTLNVTDGKTSVPAGSFGTVYVERTFTINEVMDAKTAVALVYNAKDGTFRYVPALFESGAGVTRVTVKSSLAGGVIAVAANPVSFGDISAHWAKDEISLLASRLIVNGQSAGVFAPQRTVSRAEFASMLVRSLGLQPDTLPAAAATFSDVPASSWYAADAEAAVLLGLVQGYADGSFRPDAPITREQMAVMAARAWKLLHANAAINEAGSPAAPSAPGSFNDAASISGWAKEAVDTLTARSIMNGRSGGSFAPGSNTSRAEAAVILTRLLRAGKLLNE
>NZ_CP009285.1|WP_042210979.1|1524520_1525162_-|pentapeptide-repeat-containing-protein
MNNKIEQPRIPEPELLLPQQIHSLASKDEFSRCLISGALIEYQDAARVSFDKVIFKNVTITESSLHGIELTDVIFDHCDLSNVDFSEAFMHRTEFRDCRLIGTDFTRARFQNVSVTGCIGEFAVFRFANFKAASFERSSLISADYYQSALNGLYFSECNLDQATLAGCKLKDIDLSDCEFTGLVVDLQDLDGCVISAEQAASFAGLLGLVIKY
>NZ_CP009285.1|WP_042219013.1|1524038_1524524_+|SprT-family-protein
MSNEELQLWIEQVSMNSFGVPFRHTASFNSRLTTTGGRYFTKSHNIEINPQQLAIHGREETEKIIKHELCHYHLHLAKRGYMHRDDDFKTLLARVGGSRYCQTLPGAKARKPQPYRYKLVCVACATEYLRKRKADPKRYRCGKCSGKLKLVTLEAGAGPAT
>NZ_CP009285.1|WP_042210978.1|1523556_1523916_-|hypothetical-protein
MPKMRYVILQQDQELQFVEMPEEYAYQLSALNLRLNKEIDKLTAENVPGLPRAIAECDSLELLREEHHLESGLAYINRLESAFASIQETEYPLISLLTEIRALQAQLEQWYEEEEESVH
>NZ_CP009285.1|WP_099052445.1|1523297_1523435_-|cortex-morphogenetic-protein-CmpA
MPQWLCQQLMKAYFKKDRRQIKLLNECWFFYRNSAETREFITKDV
>NZ_CP009285.1|WP_167549522.1|1523019_1523187_+|hypothetical-protein
MEPNTKDRSIEVERTEVHKKSDSSLVASTFIKYAAYIIIIFGLLFFLVKYVFPMF
>NZ_CP009285.1|WP_042210977.1|1522400_1522895_+|DinB-family-protein
MQNKISDVLVENWDYVMDVEDWQPPLKDALEGVTSEQASWKPEGAAGNSIWETVNHLTYYKERLLRKLKGLEKLPDLESNDATFTVTESGEEAWSQAVAKLKSVHASLREIIVALEEGAYEWGGSGHAPGEEVMSLILHDSYHTGQIVLVRKLQGSWPGQRSFD
>NZ_CP009285.1|WP_042210976.1|1521641_1522217_-|ABATE-domain-containing-protein
MLWEDFINSYWRNWRTGDRSTDRDRLDEPEWLTRWLEQQKLPAAGPILPVELERLKQLRGLLWDEVQRLVQGQPTESALLEQLNEYMSNGPVMRQVVWSPGGEAGISLLPQRADWEQIMAEIAASFAEALLEKESSRFRICGNPDCLWVYYDDTRNRSKRYCDDKLCGNLMKVRRFRARRKAAEDEGNLPD
>NZ_CP009285.1|WP_042210975.1|1520522_1521638_+|GGDEF-domain-containing-protein
MGPSDTSAQRQAKWIKRFLRTYWLVIALHFAAQLWAFLFLSYPMGPHEFYYDVLLYPTLLMSAVVGLTQFVDAIAPKYSFVLLFVSGTIIAMMIIHLNMDIRIIGALMLLPIFASAIFFRLDLTLFTSALQAAAFFILYRWDYWFKYYLNDFDLIAVPLFLLVGTLVAGIIIINGRELASDLEATLTAKQNLMIENAVIRKLSTTDALTGLYNHISFHEFYEKALEYGNQGAPFHLALIDIDNFKRINDKYGHRTGDAVLARVAKVIKENISPADIASRYGGEEFAILFFEKSYEEAYELADRVRQQLSETLHEELENTAVTVSIGLKSYSEGATKEQLFEEVDELLYTAKKSGKNTTLTPLQQTRHLQSV
>NZ_CP009285.1|WP_042210974.1|1516608_1516899_+|CRISPR-associated-endonuclease-Cas2
MLVLITYDVSTTSSAGQSRLRRVAKICQNYGQRVQNSVFECIVDAAQFTELKLKLKDIINLKEDSLRFYQLGNNYKNKVEHVGIKESLDLEGPLIL
>NZ_CP009285.1|WP_042210980.1|1533234_1533663_-|Lrp/AsnC-family-transcriptional-regulator
MSPYLIDDTDYRILQLLIEDSTLSHKDIGAEVHLTGQAVGARIRRMRELEIIEGYTIRWNPLRIGQNMHAFITVFLSTNAAHLPFQNFAKNHSSVAELYRISGEGCYWMRVRTVNQEALAAFLDELLGYGNYRVNLDMGQIK
>NZ_CP009285.1|WP_042210981.1|1533790_1534543_+|MBL-fold-metallo-hydrolase
MKIQLIRHAALWLEYGGVTFLVDPMLSAQGVNPPIINTANEHRNPLVSLPGPAAQWLEPDAVLVTHLHQDHWDAAAAELLSHELPVLCQEGDGERITAQGFARVTEIKDSVPASFGAVTLTRTGGQHGTGEIGERMGKVSGFVFRAEGEPVLYLAGDTIWCSEVEPVLAGHQPEVIVVNAGGASFVSGGHITMNEQDVVELCRAAPAASVIAVHMDAINHCYVTREQLSQRLESEGLLGRVAIPLDGEWV
>NZ_CP009285.1|WP_042210982.1|1535148_1536153_+|Gfo/Idh/MocA-family-oxidoreductase
MSIRIGKISFWHVHAWDYTKQAQEHGDTVIAAVWDEDAERGKKAADSLSVPFFDSLEDMLAQKDIDAVIVDAPTNMHRDIIIAAAKAGKHIFTEKVIASTLSEVNEILSEVSENGVKLTVSLPRLNDGYTLSVQDVLNQRMLGEITYVRVRLSHNGATANWLPEHFFSLEQCQGGALIDLGCHPMYLARLFLDQEVTGVSASFGYVTGKEVEDNAVATLYTSSGAIGVVEAGFVNSYSPFTIEVHGTEGTLLYGTPEEKLLVRSAKAADKGDSWNDIPLMARRESAFEQWVTHIQNNTLAAENIQIATELTRLMEAANLSAKEGRVIRLAELNP
>NZ_CP009285.1|WP_042210983.1|1536189_1537107_+|AraC-family-transcriptional-regulator
MSHFPFGIMFEKQDMLERLDISILWGHYEISVLRFHLTSFPPGKVIDFHNHAEFEFHFIPRGKGTVILGDQLYPLSEGMLYLTGPGVMHRQEADPEESMEELCLHVKITEKLREDADPWEVAEAEECVEKLRKLPPIPAQDYHRAMKCFLEAYEACDGKLTGYYTSIKHLVISILLKVTRTYDTGGMGTSAPVRDMLAYRYQYAIQYMEANSSATVTLENVAEKLNISSRQLQRIFKHIHPDKTFSRVLEDIRLQAVCSKLESGTLPIEHIAQSEGFTNATYLHSVFRKRLGMTPAAYRKSKKLN
>NZ_CP009285.1|WP_042210984.1|1537125_1538208_+|Gfo/Idh/MocA-family-oxidoreductase
MSKVYRVGIIGCGGIANGKHLPALSRQDKVQIVAFCDIIKERAEAAAEQYGGADAAVYTDYQELLRDASIDIVHVLTPNDAHAEISIAALEAGKHVMCEKPMAKTAADALRMVEAAKRTGKKLTIGYDNRFRQDSQYLKKVCESGELGHIYYGKAHAIRRRAVPTWGVFLDEEKQGGGPLIDIGTHALDLTLWMMDNYKPKVVLGTKYHELSRKEEAANAWGPWDPEKFTVEDSAFGMIVMENGATITLEASWALNSLDVDEAKCSLSGTEAGADMKDGLRINGEKHSKLYMKEIELGAGGVAFYEGKAEKATDIELRKWIEAIEQDKDPVVTPEQAYVVSRILEAIYESAQTGKAVYLN
>NZ_CP009285.1|WP_042219017.1|1538659_1539565_+|branched-chain-amino-acid-ABC-transporter-permease
MEYFIQQLINGISVGSIYALIALGYTMVYGIIKLINFAHGDVFMVGSFIGLYSAKYLANAGLPPIVVLLLSLIISMTISALLGITIERLAYKPLRKSTRIAALITAIGVSFLLEYTGVLILGPQAQGFPDIMDKKQYHLFGTSIQVESNQIMILLTTIILMLVLQYIVRYTRTGKAMRAVSFDVEAARLMGINVDRTISATFAIGSALAAAAGVIFGMTYNSVDPLMGVMPGLKAFVAAVLGGIGSIPGALVGGLLLGTVETEISSLGFSSWRDGVAFAVLILILIFKPSGLFGKNVREKV
>NZ_CP009285.1|WP_174479807.1|1539577_1540546_+|branched-chain-amino-acid-ABC-transporter-permease
MKNLNKKFWMGIIVALAFYGVIKVLLTTGVLSDVNQSMLLLIGVNIMLAVSLNLITGITGQFSIGHAGFMSVGAYTSAILTLDYNVPFVPAIIAGGLLAAVFGVLIGMPTLRLNGDYLAIATLGFGEIIRIIMLNTEYVGGASGLSGIPAKTTWTMLFFFTLISVVLINNFIRSTHGRACIAIRENEIAAEAMGINTTRYKIIAFTIGALFAGIAGGLSAHTFYVITPGSFNFLKSFEIIVMVVLGGLGSTAGSIVGAVFVTLLYTYLREFPEWRMIIYSIVLILMMIFRPSGLLGTTKFSFGKFGKKEAKANDTIEGSSAP
>NZ_CP009285.1|WP_042210985.1|1540514_1541297_+|ABC-transporter-ATP-binding-protein
MTQSKAAVLLDVKEASRSFGGLKAVSDVSLHINKGELIGLIGPNGAGKTTLFNLLTGVYPPSSGSILLNNESIGGMKPYKINHKGAARTFQNIRLFTAMTVLENVKIAFHQHAKHSLFSSMLRLPKHFKGEDEITQKAMDILKIFNLADQSHEVASNLSYGNQRRLEIARALAAGPKLLLLDEPAAGMNPNETRDLMNLIAWIREEFDLTILLIEHDMSLVMGVCNRIYVLDRGILIADGTPVEIRNNPKVIEAYLGQEA
>NZ_CP009285.1|WP_042210986.1|1541301_1542003_+|ABC-transporter-ATP-binding-protein
MLTVQGINVYYGAIHALKDLSINVKQGEIVTLIGANGAGKSTLLKTLSGLLKPKTGSIEFLDKSIVNQSVQAIVKEGLIHCPEGRRVFANMSVEENLELGAYLQDSGSLAADFQKVYNTFPRLLERKKQQAGTLSGGEQQMLAMGRAIMGHPKLLLLDEPSMGLAPLLVQDIFKIIKEVNDAGTTVLLVEQNAHQALKIADRAYVLETGRVVLEGDAKELADSDEIKMAYLGH
>NZ_CP009285.1|WP_042210987.1|1542081_1543278_+|ABC-transporter-substrate-binding-protein
MKKIGAIILSTVLTAVLASGCGNNTENSGNSASGGNAAAGTIKIGADLELTGGQASFGDSASKGAKLAVDEINAAGGILGKQLELVIADNASKSEEATQAAQKLITNDKVVTIIGASTSTNTLGIVPVATEKKIPLVAVGATNPKVTVDERSGNVNEYVFRAAFIDPFQGEVMANFALDSLKAKTAVIYTDTSSDYSKGLQKFFEETFKAKGGEVLSQESYQQKDSDFKAVLTRIKAANPDVIYLPGYYEEVGKIVKQAREMGITVPFLGGDGWDSPQLAEIAGAAALENTFMSNHYSPEDTATEVTSFVEAYKAANGGAVPDGMAALGYDALKLVADAITRAGEADPAKITEALAATKDLQLATGKITLNETHDPVKAAVVLKFVDGKQTFETKVNP

Crispr_ID: NZ_CP009285_6

• CRISPR_ID: NZ_CP009285_6
• CRISPR_location: 1656042-1656191
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP009285_6

Consensus_repeat	Method
AGTTGGAGCAGGAGCTGG	CRT

spacers of NZ_CP009285_6

>6.1|1656060|24|NZ_CP009285|CRT
GGCTGGGGCTGGGGCTGGGGCGGG
>6.2|1656102|18|NZ_CP009285|CRT
AGCTGGGGCTAGGGCAGA
>6.3|1656138|36|NZ_CP009285|CRT
CGCGGGAGCCTCAACTGGAGCAGGAGTTAGAACTGG

CRISPR arrays and Neighbor proteins around NZ_CP009285_6

CRISPR arrays

The CRISPR arrays of NZ_CP009285_6

>merge|NZ_CP009285|6|1656042-1656191|CRT
AGTTGGAGCTGGAGCTGGGGCTGGGGCTGGGGCTGGGGCGGGAGTTGGAGCAGGAGTTGGAGCTGGGGCTAGGGCAGAAGTTGGAGCAGGAGCTGGCGCGGGAGCCTCAACTGGAGCAGGAGTTAGAACTGGAGTTGGAGCAGGAGCAGG

>NZ_CP009285|6|4|1656042-1656191|CRT
AGTTGGAGCTGGAGCTGG	GGCTGGGGCTGGGGCTGGGGCGGG
AGTTGGAGCAGGAGTTGG	AGCTGGGGCTAGGGCAGA
AGTTGGAGCAGGAGCTGG	CGCGGGAGCCTCAACTGGAGCAGGAGTTAGAACTGG
AGTTGGAGCAGGAGCAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042219045.1|1658774_1659734_+|D-alanine--D-alanine-ligase	unknown	unknown	gnl|CDD|234948
NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter	unknown	unknown	gnl|CDD|224652
NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein	unknown	unknown	gnl|CDD|235016
NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	unknown	unknown	gnl|CDD|376752
NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase	unknown	unknown	gnl|CDD|234697
NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase	unknown	unknown	gnl|CDD|376754
NZ_CP009285.1|WP_042211072.1|1646957_1648049_+|threonine-phosphate-decarboxylase	unknown	unknown	gnl|CDD|273466
NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase	unknown	unknown	gnl|CDD|234838
NZ_CP009285.1|WP_081971939.1|1659730_1660945_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|181082
NZ_CP009285.1|WP_042211070.1|1644555_1645278_+|metal-dependent-hydrolase	unknown	unknown	gnl|CDD|183256
NZ_CP009285.1|WP_052429364.1|1648909_1653886_+|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_CP009285.1|WP_042211071.1|1645444_1646449_-|lipoate--protein-ligase	unknown	unknown	gnl|CDD|161920
NZ_CP009285.1|WP_081971937.1|1653997_1654846_+|adenosylcobinamide-amidohydrolase	unknown	unknown	gnl|CDD|376682
NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_CP009285.1|WP_167549525.1|1648222_1648360_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211074.1|1657298_1658759_+|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089
NZ_CP009285.1|WP_042211069.1|1643414_1644326_-|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP009285.1|WP_042211067.1|1642011_1642377_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211068.1|1642493_1643297_-|Cof-type-HAD-IIB-family-hydrolase	unknown	unknown	gnl|CDD|319818
NZ_CP009285.1|WP_042211073.1|1654898_1655864_+|cobalamin-biosynthesis-protein-CobD	unknown	unknown	gnl|CDD|234919

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042219045.1|1658774_1659734_+|D-alanine--D-alanine-ligase	gnl|CDD|234948	PRK01372, ddl, D-alanine--D-alanine ligase; Reviewed.	2.12226e-139
NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter	gnl|CDD|224652	COG1738, yhhQ, Uncharacterized member of the PurR regulon [General function prediction only].	2.57975e-54
NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein	gnl|CDD|235016	PRK02237, PRK02237, YnfA family protein.	6.51816e-44
NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	gnl|CDD|376752	pfam02277, DBI_PRT, Phosphoribosyltransferase. This family of proteins represent the nicotinate-nucleotide- dimethylbenzimidazole phosphoribosyltransferase (NN:DBI PRT) enzymes involved in dimethylbenzimidazole synthesis. This function is essential to de novo cobalamin (vitamin B12) production in bacteria. Nicotinate mononucleotide (NaMN):5,6-dimethylbenzimidazole (DMB) phosphoribosyltransferase (CobT) from Salmonella enterica plays a central role in the synthesis of alpha-ribazole-5'-phosphate, an intermediate for the lower ligand of cobalamin.	1.50433e-176
NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase	gnl|CDD|234697	PRK00235, cobS, cobalamin synthase; Reviewed.	9.58674e-53
NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase	gnl|CDD|376754	pfam02283, CobU, Cobinamide kinase / cobinamide phosphate guanyltransferase. This family is composed of a group of bifunctional cobalamin biosynthesis enzymes which display cobinamide kinase and cobinamide phosphate guanyltransferase activity. The crystal structure of the enzyme reveals the molecule to be a trimer with a propeller-like shape.	1.2539e-79
NZ_CP009285.1|WP_042211072.1|1646957_1648049_+|threonine-phosphate-decarboxylase	gnl|CDD|273466	TIGR01140, L_thr_O3P_dcar, L-threonine-O-3-phosphate decarboxylase. This family contains pyridoxal phosphate-binding class II aminotransferases (see pfamAM:pfam00222) closely related to, yet distinct from, histidinol-phosphate aminotransferase (HisC). It is found in cobalamin biosynthesis operons in Salmonella typhimurium and Bacillus halodurans (each of which also has HisC) and has been shown to have L-threonine-O-3-phosphate decarboxylase activity in Salmonella. Although the gene symbol cobD was assigned in Salmonella, cobD in other contexts refers to a different cobalamin biosynthesis enzyme, modeled by pfam03186 and called cbiB in Salmonella. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	6.34226e-97
NZ_CP009285.1|WP_042211073.1|1654898_1655864_+|cobalamin-biosynthesis-protein-CobD	gnl|CDD|234919	PRK01209, cobD, cobalamin biosynthesis protein.	1.97262e-134
NZ_CP009285.1|WP_042211068.1|1642493_1643297_-|Cof-type-HAD-IIB-family-hydrolase	gnl|CDD|319818	cd07516, HAD_Pase, phosphatase, similar to Escherichia coli Cof and Thermotoga maritima TM0651; belongs to the haloacid dehalogenase-like superfamily. Escherichia coli Cof is involved in the hydrolysis of HMP-PP (4-amino-2-methyl-5-hydroxymethylpyrimidine pyrophosphate, an intermediate in thiamin biosynthesis), Cof also has phosphatase activity against the coenzymes pyridoxal phosphate (PLP) and FMN. Thermotoga maritima TM0651 acts as a phosphatase with a phosphorylated carbohydrate molecule as a possible substrate. Escherichia coli YbhA is also a member of this family and catalyzes the dephosphorylation of PLP, YbhA can also hydrolyze erythrose-4-phosphate and fructose-1,6-bis-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, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	7.51828e-83
NZ_CP009285.1|WP_042211070.1|1644555_1645278_+|metal-dependent-hydrolase	gnl|CDD|183256	PRK11648, PRK11648, metal-dependent hydrolase.	1.04078e-05
NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase	gnl|CDD|234838	PRK00784, PRK00784, cobyric acid synthase.	0
NZ_CP009285.1|WP_052429364.1|1648909_1653886_+|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	1.37972e-12
NZ_CP009285.1|WP_081971937.1|1653997_1654846_+|adenosylcobinamide-amidohydrolase	gnl|CDD|376682	pfam01955, CbiZ, Adenosylcobinamide amidohydrolase. This prokaryotic protein family includes CbiZ which converts adenosylcobinamide (AdoCbi) to adenosylcobyric acid (AdoCby), an intermediate of the de novo coenzyme B12 biosynthetic route.	2.52612e-71
NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.74815e-50
NZ_CP009285.1|WP_042211074.1|1657298_1658759_+|PLP-dependent-aminotransferase-family-protein	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	1.58955e-115
NZ_CP009285.1|WP_042211069.1|1643414_1644326_-|DMT-family-transporter	gnl|CDD|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	5.39021e-10
NZ_CP009285.1|WP_081971939.1|1659730_1660945_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|181082	PRK07682, PRK07682, aminotransferase.	0
NZ_CP009285.1|WP_042211071.1|1645444_1646449_-|lipoate--protein-ligase	gnl|CDD|161920	TIGR00545, Probable_lipoate-protein_ligase_A, lipoyltransferase and lipoate-protein ligase. One member of this group of proteins is bovine lipoyltransferase, which transfers the lipoyl group from lipoyl-AMP to the specific Lys of lipoate-dependent enzymes. However, it does not first activate lipoic acid with ATP to create lipoyl-AMP and pyrophosphate. Another member of this group, lipoate-protein ligase A from E. coli, catalyzes both the activation and the transfer of lipoate. Homology between the two is full-length, except for the bovine mitochondrial targeting signal, but is strongest toward the N-terminus. [Protein fate, Protein modification and repair].	5.6807e-120

Protein sequences

>NZ_CP009285.1|WP_042211073.1|1654898_1655864_+|cobalamin-biosynthesis-protein-CobD
MKLAIILLAAYVVDRIVGDPRNLPHPVIYMGKAISAIERLIRRFAARPRALKRAGLLLPLLVAGGAWALTALLVMLLYRISPWLAGAAEVWLISTTIASKGLKDAGMAVFAELRQGDIPAARRALGMIVGRDTARLESPEIVRGTVETVAENIVDAIISPLFFALLGGAPLAMAYRAVNTLDSMVGYKNDKYRDLGWASARLDDVANYIPARITALLLTLCAALLRLDWRRCWRTVRRDARLHPSPNSGYPESAVAGALGIRLGGENVYHGVTSFRAYMGDPLRTMEPEDIIVTSRMMMLSSAIFVCLCAAVALLWNGIGG
>NZ_CP009285.1|WP_081971937.1|1653997_1654846_+|adenosylcobinamide-amidohydrolase
MNSLLCERSGWNVKEVQVKLPFNLDGGLTVYRSRVWQGLTLEWREGHLLLEFPAEADSISSAVYGGGTGRLKRAVNQYVTRDYECSNPVRDMENKLQEWGYPLEGCAGLMTAVPLEHAAVAEEDTGSAGIMCCVTAAAGNAARAGSQRSVLAAYRPGTINIMLGIDGWLSPSAMVNAVMTATEAKAAALADLGITDSENGLTATGTTTDAIVLAVSGSHRYAAEHVYAGTATDLGGAIGRLVYSAVTESLRSVKAAEAVLRAQAAQPELQGQPGQQSKGGRG
>NZ_CP009285.1|WP_052429364.1|1648909_1653886_+|S-layer-homology-domain-containing-protein
MLRIPLRKIPVLILLASLVLSSAPFGEPPAAYGAGGTAAAVSSAVLDITQSKVEGEYALDLSEVGNVDWLHLKGNGPDDIIQIKKAVPSSVTFSVYGNDTTGTEGKPDRGSDGNYLSYSWNDGMAGYERAVKDTGFGVFFPKNRDSGIYGNVGWTFKIAPQPQESTVVFGIGLWQAKAAVKIYADMNLMETKEISAGGTSEVYKYQIKVPANVQLRVEGLQAETLSRYGNMSFSGLAISSKEVADKSLLQLAYNQVKDKLQGVYTDASWQDFAKARIQAKEVLDKPDALQAEIDTALSLLEQKQAALVRRETNLMIDYTGAAENEYEFGSNGDQQDRYQTFTAQESFEMQYAQVNVRKMSNNVSDLTVKLYGTDPSGFPAGAPLAETVVGRDRVADGEMTTIPLRYSLTGNTRYALVVSQKNLSAGKYRWMVMKKNGETASEFFGKNVSGAFQSEAHLGTGILRIIKNTDVDRTALQALIDDIAKSNYNSRLYTIPSWSALEAALANAGLVLNDFDADQEEIDAALSHLQEASDQLEINMDMAAIAGQIDLISRAVIKGYTLSSLNTLNEAVQAAKALDANAPDNEKLTAFSAVLEAIHNLKTAGKYQYDTHAQMTAAFGFEGDKNASLAFLDGSYQIGGSRPEQHGPVAPKQMVTFGVADTSNIKWTKGEGYLPVMISEYTKNKVDYKIETFANKHTVDQKDYVVNYSRVTAANHSGELMLLPVVSGNLVPINADAVNTYTVQPGGSVVREYAIEADKYEYFDKNLTRFTSLTKEQVAGLGTFEANYIEMKAYWLTRLSTIVDIGLPNQELENAFKSGYIDTLIIKDDTYLHVGENGYARLFSHDTLGILVNLIQSGDFAHAQDYLKSIPLTGGINIETGQVDSNLYWDTNWKIPWAYAVYLSKTGDASIFDEQMTADDGSTGTVFEKRVKFGARTIESDRNADGIMKKTYAIDSEGNWTIDNYSALTGLTAYEYVTRELYRLKNDETYLQEAEWAKARYDDLLAKFTAKLQQTITEEGLDYIPASVVETNDENRMSDSRDANWASMFLFGRWHWDGYLYGAEQPEDNINLKLLDDTYSYGINRRIQEDTTDSPYNFGGYPHGFYSSAYNAGYGSAALRGEEYRDMGIKAYEFMIENSMSGPFSWWEGINYPVAGSPWAQTNDQLNLQNTPGGGGSAQHMWGQSVNSKVLIDSLIAERIYDQNQKAEIIVGRGIPKEWVKDAARNNNVVASVQNYPALQGGRVGYSIVRQDNQLVVTFSSDLNQSKVEAGGASFSVQLPSMVNNITDVSAGILDNGKGIVTVPLNTASVTITLGDLPKPLAVNLDKDKLEIVYAEGDLQTSVTKDVILPAAGEHGSEITWTSSSPDIISSKGEVKRPVSTTVVTLTAILKKDGAEAQKSFVLTVLKADTKPDGGTDTGNNGNNGNNGNNSNNSNNSNNGNAGNNTGNAGTIGTIVTTDNKGSTGSTGNTGDGGITTQPAFKDVEKHWAKENIITAAQRKLINGYEDGTFRPDGAVTRSEFAVILGRALQADFAQSGLTFTDAGSIPSWAKPYVAAAVNSGWITGYTDQSFRPGGNITRLEMIAMIVRALGWKTDPQAKAAFADAELIPSWGQPYAAAAYEAGLVEGQENNRLAPNDQATRAEAVTLILRLLDKTEQQ
>NZ_CP009285.1|WP_167549525.1|1648222_1648360_-|hypothetical-protein
MHTCSEVSRRTVGGWNVTAGGWNVTAGGCHADAGGGTLTLAAGTL
>NZ_CP009285.1|WP_042211072.1|1646957_1648049_+|threonine-phosphate-decarboxylase
MLEKYGHGGDLLTAAELYGENSGGFLDFSANINPLGPPPGVLALLRDAVSAITAYPDPGHRRLKALLAESLGVGTDWITVANGAAESMALLLLATAPRRVGIVEPCFSEYRQLAEQFGAEVLSVQGTLASDYRASVDEISGLLEQTDLLFLGQPNNPNGVQYPLDELRLLAQRAEDSGTVLAVDEAFTDFIPEADRQSLLPELGAYRHTVLVRSMTKFFAIPGLRLGFTAAHPELAAAMTGKQVTWSVNGLALLAGEACLQSGDGYGQETRALIAAERQLLRQGLLELGCEVPPGEANFLLLRLPAPWSAQEIQQRLGAGGILVRSCAMYPGLEPGHIRVAVKGRADNARLLREMGTLLRAGI
>NZ_CP009285.1|WP_042211071.1|1645444_1646449_-|lipoate--protein-ligase
MLFIDNTGITDASINLAIEEFALKNLPMDESYLLFYINSPSIIIGKHQNTIEEINQEYVKDNNIQVVRRLSGGGAVYHDLGNLNFSFITKDDGQSFHNFLKFTQPVIDYLQAMGVNAELSGRNDLQVGEQKISGNAQFSTRGRMFSHGTLMFDLNLDDVQASLNVNPEKFKSKSTKSVRSRVANIKELLGNPEMTIEQFREGLLRSIFGMEASEVPQYKLTMDDWVRINEISKEHYQNWDWNYGLSPKSNVKHTRKFPAGLVDIRMDIEDSIIREIKIYGDFFGVGDVADVENALRGKRYAEAEVREALADLDLKHYFGRIEPEDFIGLVFLEE
>NZ_CP009285.1|WP_042211070.1|1644555_1645278_+|metal-dependent-hydrolase
MMGKSHLVISTGVTLSAMSLLGLEITLPAVAVAVVSSLLPDIDEPNSLLVRKAVPEFLLRILQVSLIGAAIYLYFAGIAAPPWNIALALLVGSVSFLPGRRLRHLVMLLIALALFAFADAYDPWNYIAACVLVVASVVPHRGITHTLYAVAGWGALLYFVSPGMNDGGSLWIAGSMSYGLHLLADSLTQRGITPLPPLPVKLRLKLMSTGTKKGNAVEKVCVMLTLALVVYVFVLTPSLV
>NZ_CP009285.1|WP_042211069.1|1643414_1644326_-|DMT-family-transporter
MNRSRIADLSLLLVAMMWGCTFLIVQSAVRMLPPLAFNSIRFTGAAMLLALITAVFYRQEWKKLSLRMVLHALLLGLLLFLGYGFQTMGLLYTTTSNTGFITGLSVVLVPFLSLALLKHAISRYTWFSAGLAAVGLYLLTFTGSAFSLNKGDGLILLCAAFFALQIAYTGIYAPRYPALPLAALQLAFVGLFSILASLLVDGPAPLMHSGELLAKPEVLWAMLISIGPTSAFAFWIQTACQKYTTPSRVAIIYATEPVFAAVTGLLFGGETLGLSAALGCGCILAAMLLAELSPEPARTQAEG
>NZ_CP009285.1|WP_042211068.1|1642493_1643297_-|Cof-type-HAD-IIB-family-hydrolase
MYKLIAIDIDDTLINDDKEVTPATQTALEQAVAAGVVVTLATGRAYASAQAIARQTGLNVPIITYQGALVKNLLDEEVLYERYVPQDAVRKLFQYCVEHDLHLQTYIDDKLYAREENQKLIDYAALNKTQYYIEPNWEEKLVPQKTPKMLIIDDPAFLDELSPILRNLLGDSVHITKSKPHFLEIMHHEGTKGLALEFLAKHFGCDLSETIAVGDSWNDHEMLEAAGLGVAMANAIPALKEIADFVTLSNNEDGVKFAIDKFILGAE
>NZ_CP009285.1|WP_042211067.1|1642011_1642377_-|hypothetical-protein
MEEVSAADQLESIKSWQSTIKKLENAFAQMTQKGTNITLVKKRLNASHIGLAVLENAWSQKPHLYSHEDITEAGKILSGLVSSVEHSYAKSKAGSPQQTLLERRLKALNLAVQAIDGLSAK
>NZ_CP009285.1|WP_042211074.1|1657298_1658759_+|PLP-dependent-aminotransferase-family-protein
MFKDFKLIAGRPVYIQVKDYMKHLIIKSALQGGQKLPSTRELSTLLKVSRNSIISAYESLEDDGFAYTVQGQGSYVSPGAGAGHGGPEAASWSMDWKERISGHALLAEELDIMKRGIRAEKGTISFTSIAPDESLFDLEHVRRAFLERMSVEGNVLLNYGYAKGYKPLIDYLRQYMEHKGVDMRGKDLLITNGFTEGFDIVLTALGKRHGAVICENPTHHTAVKNLKLHGFGIHGVTMERDGIHLGELKRALDEREYDCAYLVPSYHNPTGIVMSPEKRQGLMKLMQDYKVPVIEDGFNEELRYSGAHVAPLIAAAGGGNSVVYLGSFSKVLFPGLRVGWVLADQELIYYLESVKRARSIHTSTLDQSILYQYLLGGNLEKYLKKARLEYKRKYELTLACCKEHIPYASLSGDGGLHLFVTFAEGFNTRELLAACHGQGVIFTAGDIFFTDGTGQNTLRLGFSRVADEDIRRGIEIIGRTARQLMR
>NZ_CP009285.1|WP_042219045.1|1658774_1659734_+|D-alanine--D-alanine-ligase
MRVGVIMGGVSSEYEVSMNTGREMLKALDPAKYIGIPVPITSRKELLEGVAGLDFALLALHGTYGEDGTVQGALETLGIPYSGSGVLSSSLCMDKGLAKTVIRSKSIPTPDWLCWDSINEYDPEAVDRLGYPVMVKPNSGGSSIGMTKVNHPQELRGAVEKAFAADCSVLIERYTTGQEITCSILGGEMLPVIGIQSLGADWFDYSAKYEQGGAKEQIIQLPAEVEERVRTAALACYRALKCAVYARVDMLLVDGIPYVLEVNTLPGMTATSLLPQSAKAAGISFTRLLDEIITGSMRERGELDGAAAAQQVQQGGVRL
>NZ_CP009285.1|WP_081971939.1|1659730_1660945_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MKRVQSALPLNRLPRISVHNDPVTPRLREIPPSGIRAFFDLAAGNNDIISLGVGEPDFTTPEQVRAACVRALNEGETAYTPNAGRMELREEISGYLRNGFALTYDHADEILVTVGSSEAVDLALRAFIAPGDEILIPSPGYVAYAPIAYLNGGTLATVETTAEQGFKLTAEALRQAITPRSKLLMVNFPSNPTGAVMTYEDWLPVAEVVKEHGLIVISDEIYAELTYDSTHVSIASLPGMKERTVVISGFSKAFAMTGWRVGYACGNRELLAAMLKIHQYTAMCAPVLGQIAAAESLRSALPDKDRMKACFKDRRTLFVDGLRSAGLPCHMPQGAFYAFASIARTGMSSEEFALRLLKEAGVAVVPGHVFGAGGEGYIRCSYAASTAKLTEALERLEGFMKVKI
>NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase
MITAIQEVTGRIAPPDEKATLRAVLRLNSLTKPPGSLGRLEALAVRLAGISKVEQPCYSKRTVVVMAADHGVCCEGVSAFPQEVTMQMAYNFLSGGAAVNVLARQGGAEVQFVDIGINGDITHPQLIDRKVRRGTDNMAAGPAMSRDDALRAILAGVQVAQEAVKNGTEIFITGEMGIGNTTASAAVLCALEGIPPETAAGRGTGIDDERLRHKISVIERALQVNTPNPADPIDVLSKVGGLEIAGLAGLILGAAALRIPVILDGFISGAAALVAKALAPESTAYMIASHVSGEQGHKLMLDRLGLEALLDLGLRLGEGTGGALCLHFIEAVCRIMREMATFESAGVSGSESV
>NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase
MSILVTGGARSGKSGFAERLTRKLADPQQAVYVATGQAFDEEMKARIALHRQQREEGGFRWETLEEPLELSVLLERQSGSGQAVLVDCLTLWLSNQLLAVEERSDRQQLVEEAIAGLEQSVSSFQGTLILVTNEVGDGIVPEYSLGRLYRDLAGRMNARLARQCEQVFLVTAGIPLELKSREYLL
>NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase
MSARGDAAAAFQFLSRFPVKYSPDFSPELLRRSVVYYPLVGAAIGLSAALGAAAAAWLLPVWPAAVITLILWVGLTGGLHLDGWMDCADALLSYRSRERMLEIMKDSRVGAMGVLACVLLLLLKASLLAALIEGGSYSMLPLLLLPPVWSRWYMVRAMARYPLARGNEGLAASFGGLPARLERRARLSAALLTLAAAAAPLALGAGSGAWPQLAAAAILAPAAAAACGMLAARRIGSRLGGLTGDVYGALGELLETVVLLVLVLLQHNL
>NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase
MLQGTASDVGKSLVTAAIGRIMTRDGYRTAPFKSQNMALNSYVTADGKEIGRAQGMQAEAFGITATSDMNPILLKPSGEMSAQIVVHGVPHAALSAREYREKFLPEAKGTVMDALGRLREAYDIVLMEGAGSPAEINLKARDIVNMNLAGWADAPVLLVADIDRGGVFAFIVGTLELLEPHERARVKGFIINKFRGDVSLLQPGLDWLEERTGIPVLGVLPFLPQLRIEAEDSVVLEGTSGRLREESARELDIAVIRYPRISNFTDFDPLADEPDTAVRYVMSADELGTPDVIILPGTKNTAADLQYLREQGFPEAIERALEQGTQQLAGICGGYQMLGLKLLDPHAVESTEPGESEGLGYLPLSTAFLQQKTTVRVSGTLAADHPLQLGTEALASIGGMPITGYEIHMGTTTNHDAASVRSLFMLAGPEGQAVPEGWGTPDGRIWGSYLHGLFHNDKLRRSWLDGLRTAKGLAPLTVTFSAAALREQEFDRLADAVRAHLDMNAVYNIMGLRGRGE
>NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein
MAAAVLLFIVAGLAEIGGGYLVWLWLRESRPLWYGLVGSVILIAYGIIPTLQKFPSFGRVYAAYGGVFIVLAVLWGWLVDRKTPDLYDWIGAGICVIGVSVILWAPRH
>NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein
MFRFKKSISRKFTLLLFVVLLLTSLLLSISFYFISTNIINSYVLPQINKSLTASAQDVYKNLNATSAQQALNKNEQAGTNVEFYFEEKRKQHDVETIFLIDLKEGKATVLVADHSAKLKREESIEVLPAMEQASKGKAGLSEIYSDSHGIHKSAFVGVPGTTMLVGVSSDVGFIQEKMSNILWTSAGITLLALIVGLSGATLMSRRIIRPIKLLAAYSNKLAGGDFTEALTIKGTDEVGQLSESFRIMSERLKEMIGHVLDTSGTVVADSNDLKERVQILNNMAEQSAISVEEIGKGSTTIASSALDNSRAMDEINIGIQHIASAAGEVTEQISEASAEAMGGNDIAQSAVQQMRQVEQASVQSLEQFRIMNERSLMIGEVVQGITEITKQIQMLSLNASIEAARAGEHGRGFAVVAGEVRKLSEQSKESNEQIREFLLGLQEDMNHSVSEMNHVNAEVASGVNKVVEAGNAFNHLLILIQSINHSIQSVSAATQQISAGTEEVSASVEETAQITAKSQQSADTLGENSARQHQELEGHALTVEHLHEQAVKLQKAAQQFKI
>NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter
MFNLLWGILFVVVNFVFFLLCYRLFGKKGLYAWVGMATVVANIQVAKTIAMPFDIVMTLGNTMYVTLYMTSDLLNERYGRAEARNAVWFGFFTLLMTTVIMQMVLIFEPQETDIAQSSLQTIFGLMPRLALGSLTAYFISQFLDVRLYAWIRKYYGSSRQLWIRSNGSTMISSFVDTLIFCTIAFAGTYDLKVWTEILLTTYLAKFLLTGAGTPVLYLARSFKFAEEEQTVRPQETKRNIS

Crispr_ID: NZ_CP009285_7

• CRISPR_ID: NZ_CP009285_7
• CRISPR_location: 1672981-1673070
• CRISPR_type: TypeV
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: cas14j

Consensus repeat of NZ_CP009285_7

Consensus_repeat	Method
AAGTTTTGTGAGCATCCGCTTCCTG	CRISPRCasFinder

spacers of NZ_CP009285_7

>7.1|1673006|40|NZ_CP009285|CRISPRCasFinder
AATCATCATCATACAAAACTCGCATCGGAAGCATAATCTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_7

CRISPR arrays

The CRISPR arrays of NZ_CP009285_7

>merge|NZ_CP009285|7|1672981-1673070|CRISPRCasFinder
AAGTTTTGTGAGCATCCGCTTCCTGAATCATCATCATACAAAACTCGCATCGGAAGCATAATCTTAAGTTTTGCGAGCATCCGCTTCCTG

>NZ_CP009285|7|6|1672981-1673070|CRISPRCasFinder
AAGTTTTGTGAGCATCCGCTTCCTG	AATCATCATCATACAAAACTCGCATCGGAAGCATAATCTT
AAGTTTTGCGAGCATCCGCTTCCTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter	unknown	unknown	gnl|CDD|224652
NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein	unknown	unknown	gnl|CDD|235016
NZ_CP009285.1|WP_042211081.1|1669025_1670120_-|aminopeptidase-P-family-protein	unknown	unknown	gnl|CDD|223085
NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase	unknown	unknown	gnl|CDD|234697
NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase	unknown	unknown	gnl|CDD|376754
NZ_CP009285.1|WP_042211084.1|1674872_1675376_+|N-acetyltransferase	unknown	unknown	gnl|CDD|224168
NZ_CP009285.1|WP_042211083.1|1674717_1674897_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042219052.1|1672216_1672945_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293807
NZ_CP009285.1|WP_042211082.1|1673077_1673407_-|chaperone-CsaA	unknown	unknown	gnl|CDD|182232
NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase	unknown	unknown	gnl|CDD|234838
NZ_CP009285.1|WP_042211086.1|1675852_1676113_+|YqkE-family-protein	unknown	unknown	gnl|CDD|315655
NZ_CP009285.1|WP_042211089.1|1680783_1681287_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|170033
NZ_CP009285.1|WP_174479850.1|1670552_1671704_+|PQQ-dependent-sugar-dehydrogenase	unknown	unknown	gnl|CDD|369642
NZ_CP009285.1|WP_042211088.1|1679247_1680534_+|ATP-binding-protein	unknown	unknown	gnl|CDD|365803
NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_CP009285.1|WP_042219056.1|1676255_1677329_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14j	-	gnl|CDD|223747
NZ_CP009285.1|WP_042219055.1|1673589_1674432_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|212492
NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	unknown	unknown	gnl|CDD|376752
NZ_CP009285.1|WP_174479851.1|1677827_1679246_+|RtcB-family-protein	unknown	unknown	gnl|CDD|376465
NZ_CP009285.1|WP_042211085.1|1675413_1675761_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042219056.1|1676255_1677329_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14j	-	6.6e-99	326.7	6.7

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter	gnl|CDD|224652	COG1738, yhhQ, Uncharacterized member of the PurR regulon [General function prediction only].	2.57975e-54
NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein	gnl|CDD|235016	PRK02237, PRK02237, YnfA family protein.	6.51816e-44
NZ_CP009285.1|WP_042211081.1|1669025_1670120_-|aminopeptidase-P-family-protein	gnl|CDD|223085	COG0006, PepP, Xaa-Pro aminopeptidase [Amino acid transport and metabolism].	1.75633e-116
NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase	gnl|CDD|234697	PRK00235, cobS, cobalamin synthase; Reviewed.	9.58674e-53
NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase	gnl|CDD|376754	pfam02283, CobU, Cobinamide kinase / cobinamide phosphate guanyltransferase. This family is composed of a group of bifunctional cobalamin biosynthesis enzymes which display cobinamide kinase and cobinamide phosphate guanyltransferase activity. The crystal structure of the enzyme reveals the molecule to be a trimer with a propeller-like shape.	1.2539e-79
NZ_CP009285.1|WP_042211084.1|1674872_1675376_+|N-acetyltransferase	gnl|CDD|224168	COG1247, COG1247, Sortase and related acyltransferases [Cell envelope biogenesis, outer membrane].	1.05051e-44
NZ_CP009285.1|WP_042219052.1|1672216_1672945_-|MBL-fold-metallo-hydrolase	gnl|CDD|293807	cd07721, yflN-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis yflN; MBL-fold metallo hydrolase domain. This subgroup includes the uncharacterized Bacillus subtilis yflN protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of 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.	8.18109e-67
NZ_CP009285.1|WP_042211082.1|1673077_1673407_-|chaperone-CsaA	gnl|CDD|182232	PRK10089, PRK10089, chaperone CsaA.	7.48274e-63
NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase	gnl|CDD|234838	PRK00784, PRK00784, cobyric acid synthase.	0
NZ_CP009285.1|WP_042211086.1|1675852_1676113_+|YqkE-family-protein	gnl|CDD|315655	pfam13025, DUF3886, Protein of unknown function (DUF3886). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 90 amino acids in length. There are two completely conserved L residues that may be functionally important.	1.43303e-07
NZ_CP009285.1|WP_042211089.1|1680783_1681287_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|170033	PRK09644, PRK09644, RNA polymerase sigma factor SigM; Provisional.	2.57944e-47
NZ_CP009285.1|WP_174479850.1|1670552_1671704_+|PQQ-dependent-sugar-dehydrogenase	gnl|CDD|369642	pfam07995, GSDH, Glucose / Sorbosone dehydrogenase. Members of this family are glucose/sorbosone dehydrogenases that possess a beta-propeller fold.	8.61554e-114
NZ_CP009285.1|WP_042211088.1|1679247_1680534_+|ATP-binding-protein	gnl|CDD|365803	pfam00004, AAA, ATPase family associated with various cellular activities (AAA). AAA family proteins often perform chaperone-like functions that assist in the assembly, operation, or disassembly of protein complexes.	6.88433e-23
NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.74815e-50
NZ_CP009285.1|WP_042219056.1|1676255_1677329_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl|CDD|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.90145e-56
NZ_CP009285.1|WP_042219055.1|1673589_1674432_+|SDR-family-oxidoreductase	gnl|CDD|212492	cd05327, retinol-DH_like_SDR_c_like, retinol dehydrogenase (retinol-DH), Light dependent Protochlorophyllide (Pchlide) OxidoReductase (LPOR) and related proteins, classical (c) SDRs. Classical SDR subgroup containing retinol-DHs, LPORs, and related proteins. Retinol is processed by a medium chain alcohol dehydrogenase followed by retinol-DHs. Pchlide reductases act in chlorophyll biosynthesis. There are distinct enzymes that catalyze Pchlide reduction in light or dark conditions. Light-dependent reduction is via an NADP-dependent SDR, LPOR. Proteins in this subfamily share the glycine-rich NAD-binding motif of the classical SDRs, have a partial match to the canonical active site tetrad, but lack the typical active site Ser. This subgroup includes the human proteins: retinol dehydrogenase -12, -13 ,and -14, dehydrogenase/reductase SDR family member (DHRS)-12 , -13 and -X (a DHRS on chromosome X), and WWOX (WW domain-containing oxidoreductase), as well as a Neurospora crassa SDR encoded by the blue light inducible bli-4 gene. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	4.86015e-112
NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	gnl|CDD|376752	pfam02277, DBI_PRT, Phosphoribosyltransferase. This family of proteins represent the nicotinate-nucleotide- dimethylbenzimidazole phosphoribosyltransferase (NN:DBI PRT) enzymes involved in dimethylbenzimidazole synthesis. This function is essential to de novo cobalamin (vitamin B12) production in bacteria. Nicotinate mononucleotide (NaMN):5,6-dimethylbenzimidazole (DMB) phosphoribosyltransferase (CobT) from Salmonella enterica plays a central role in the synthesis of alpha-ribazole-5'-phosphate, an intermediate for the lower ligand of cobalamin.	1.50433e-176
NZ_CP009285.1|WP_174479851.1|1677827_1679246_+|RtcB-family-protein	gnl|CDD|376465	pfam01139, RtcB, tRNA-splicing ligase RtcB. This family of RNA ligases (EC:6.5.1.3) join 2',3'-cyclic phosphate and 5'-OH ends. They catalyze the splicing of tRNA and may also participate in tRNA repair and recovery from stress-induced RNA damage.	3.79148e-128
NZ_CP009285.1|WP_042211085.1|1675413_1675761_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	5.18324e-33

Protein sequences

>NZ_CP009285.1|WP_042219052.1|1672216_1672945_-|MBL-fold-metallo-hydrolase
MNFGPNVTVLTVPMLSPVMGPTVIYPVLLKDGDGLTLIDTGMFGQYDSLVQAILQAGEQLSSIKRIILTHQDIDHIGNLPVLVREIPGVQLFAHPGDIPVISGSESMLKMTPERITGMPQAFQEQINAFLEQLTQLGEITELHDGDQLPWGGGAEVIHTPGHTPGHICLYLPQEKLLLAADELRVADGRLAGPAESATPDMPLALRSLRKLDGLPVQSIVCYHGGRYDGSPQVLIDSLAGGL
>NZ_CP009285.1|WP_174479850.1|1670552_1671704_+|PQQ-dependent-sugar-dehydrogenase
MTTMTETPVTRTPGASASVGKGASGSTQAPEVTAAATKPPASSAFPYTAQPLAHGLNVPWEMAFAPDGRIFFTERPGSLRVIENGKLREAPLLELLAPFVSKGEGGLLGLALDPEFESNGFAYVYHSYRNAEGGVANRVLRIKIGSSKAEIKEVLLDNIPGDTNHNGGRIKIGPDGYLYITTGERYEPELAQDKTSLGGKILRITTSGGIPEDNPWPGSPVYSMGHRNPQGLAWQPESGVLYSSEHGQSRHDELNIIQAGANYGWPLIEGDETGAAKLKLKTPLAHSGEETWAPSGMTFITQGPWSGELLVAGLAGQELLRVSLSPSDGEPAITALFKEKYGRIRNVAEGPDGTLYLMTNNRDGRGSPRAQDDKLIALRPDWK
>NZ_CP009285.1|WP_042211081.1|1669025_1670120_-|aminopeptidase-P-family-protein
MNEALLKLERGLTGGGLDALLVTDPKHVYYLTGFASNPHERFLGLLLIRGEEPVLIVPALDAEAAHAASSVKTILTHSDTDNPYELLKSRFGGANPGSFGIEKEHFSVSRYELLADAIPAGSFSDIGHLLRAMRAVKTPEEIRIMKHAAELVEEVLRRGLSHVKAGVSENELVAELEYLMKKVGASGPSFDTMVLSGPNTALPHGVPGERIIQPGDLLMFDLGVYAGGYASDITRTFAVGEVNSKLTDIYNTVLAANEAGIAASVAGATFGSVDKAARDVIEAAGYGEYFMHRVGHGLGMDTHEYPSLHGLNTDIIANGNVFTVEPGIYVPNLGGVRIEDDVLVTAEGPQTLTSFPKELTVLSL
>NZ_CP009285.1|WP_042211080.1|1668232_1668958_+|queuosine-precursor-transporter
MFNLLWGILFVVVNFVFFLLCYRLFGKKGLYAWVGMATVVANIQVAKTIAMPFDIVMTLGNTMYVTLYMTSDLLNERYGRAEARNAVWFGFFTLLMTTVIMQMVLIFEPQETDIAQSSLQTIFGLMPRLALGSLTAYFISQFLDVRLYAWIRKYYGSSRQLWIRSNGSTMISSFVDTLIFCTIAFAGTYDLKVWTEILLTTYLAKFLLTGAGTPVLYLARSFKFAEEEQTVRPQETKRNIS
>NZ_CP009285.1|WP_042211079.1|1666120_1667809_-|methyl-accepting-chemotaxis-protein
MFRFKKSISRKFTLLLFVVLLLTSLLLSISFYFISTNIINSYVLPQINKSLTASAQDVYKNLNATSAQQALNKNEQAGTNVEFYFEEKRKQHDVETIFLIDLKEGKATVLVADHSAKLKREESIEVLPAMEQASKGKAGLSEIYSDSHGIHKSAFVGVPGTTMLVGVSSDVGFIQEKMSNILWTSAGITLLALIVGLSGATLMSRRIIRPIKLLAAYSNKLAGGDFTEALTIKGTDEVGQLSESFRIMSERLKEMIGHVLDTSGTVVADSNDLKERVQILNNMAEQSAISVEEIGKGSTTIASSALDNSRAMDEINIGIQHIASAAGEVTEQISEASAEAMGGNDIAQSAVQQMRQVEQASVQSLEQFRIMNERSLMIGEVVQGITEITKQIQMLSLNASIEAARAGEHGRGFAVVAGEVRKLSEQSKESNEQIREFLLGLQEDMNHSVSEMNHVNAEVASGVNKVVEAGNAFNHLLILIQSINHSIQSVSAATQQISAGTEEVSASVEETAQITAKSQQSADTLGENSARQHQELEGHALTVEHLHEQAVKLQKAAQQFKI
>NZ_CP009285.1|WP_042211078.1|1665408_1665735_+|YnfA-family-protein
MAAAVLLFIVAGLAEIGGGYLVWLWLRESRPLWYGLVGSVILIAYGIIPTLQKFPSFGRVYAAYGGVFIVLAVLWGWLVDRKTPDLYDWIGAGICVIGVSVILWAPRH
>NZ_CP009285.1|WP_042219049.1|1663852_1665406_+|cobyric-acid-synthase
MLQGTASDVGKSLVTAAIGRIMTRDGYRTAPFKSQNMALNSYVTADGKEIGRAQGMQAEAFGITATSDMNPILLKPSGEMSAQIVVHGVPHAALSAREYREKFLPEAKGTVMDALGRLREAYDIVLMEGAGSPAEINLKARDIVNMNLAGWADAPVLLVADIDRGGVFAFIVGTLELLEPHERARVKGFIINKFRGDVSLLQPGLDWLEERTGIPVLGVLPFLPQLRIEAEDSVVLEGTSGRLREESARELDIAVIRYPRISNFTDFDPLADEPDTAVRYVMSADELGTPDVIILPGTKNTAADLQYLREQGFPEAIERALEQGTQQLAGICGGYQMLGLKLLDPHAVESTEPGESEGLGYLPLSTAFLQQKTTVRVSGTLAADHPLQLGTEALASIGGMPITGYEIHMGTTTNHDAASVRSLFMLAGPEGQAVPEGWGTPDGRIWGSYLHGLFHNDKLRRSWLDGLRTAKGLAPLTVTFSAAALREQEFDRLADAVRAHLDMNAVYNIMGLRGRGE
>NZ_CP009285.1|WP_042211077.1|1662760_1663570_+|adenosylcobinamide-GDP-ribazoletransferase
MSARGDAAAAFQFLSRFPVKYSPDFSPELLRRSVVYYPLVGAAIGLSAALGAAAAAWLLPVWPAAVITLILWVGLTGGLHLDGWMDCADALLSYRSRERMLEIMKDSRVGAMGVLACVLLLLLKASLLAALIEGGSYSMLPLLLLPPVWSRWYMVRAMARYPLARGNEGLAASFGGLPARLERRARLSAALLTLAAAAAPLALGAGSGAWPQLAAAAILAPAAAAACGMLAARRIGSRLGGLTGDVYGALGELLETVVLLVLVLLQHNL
>NZ_CP009285.1|WP_042211076.1|1662206_1662764_+|bifunctional-adenosylcobinamide-kinase/adenosylcobinamide-phosphate-guanylyltransferase
MSILVTGGARSGKSGFAERLTRKLADPQQAVYVATGQAFDEEMKARIALHRQQREEGGFRWETLEEPLELSVLLERQSGSGQAVLVDCLTLWLSNQLLAVEERSDRQQLVEEAIAGLEQSVSSFQGTLILVTNEVGDGIVPEYSLGRLYRDLAGRMNARLARQCEQVFLVTAGIPLELKSREYLL
>NZ_CP009285.1|WP_042211075.1|1661148_1662210_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase
MITAIQEVTGRIAPPDEKATLRAVLRLNSLTKPPGSLGRLEALAVRLAGISKVEQPCYSKRTVVVMAADHGVCCEGVSAFPQEVTMQMAYNFLSGGAAVNVLARQGGAEVQFVDIGINGDITHPQLIDRKVRRGTDNMAAGPAMSRDDALRAILAGVQVAQEAVKNGTEIFITGEMGIGNTTASAAVLCALEGIPPETAAGRGTGIDDERLRHKISVIERALQVNTPNPADPIDVLSKVGGLEIAGLAGLILGAAALRIPVILDGFISGAAALVAKALAPESTAYMIASHVSGEQGHKLMLDRLGLEALLDLGLRLGEGTGGALCLHFIEAVCRIMREMATFESAGVSGSESV
>NZ_CP009285.1|WP_042211082.1|1673077_1673407_-|chaperone-CsaA
MATIEDFLKLDMRIGTILTAEPFPEARKPAIKLQIDFGEIGIKASSAQITKRYTPEELIGRQIAAVVNFPPRRIAGFLSEVLVLGGVPEEGDVILLAPGHRVPDGTPVA
>NZ_CP009285.1|WP_042219055.1|1673589_1674432_+|SDR-family-oxidoreductase
MKGKTVLITGANSGMGLAAAVEMARRGASVIMACRSRKRGEEALAEAVRQSGSDQIRLMLCDLSSFASIRAFAAEFTASYPVLDVLINNAGVVAIRRELTADGYEQDLGVNHLGHFLLTNLLLGTLKAAEQGRIVVVASGAYKIGKLHLEDHTLLRGFNPAKAYARSKLANILFTRELAARLKDTRVTVNCVHPGAVGTSIGVNRETGFGRSLLKLLSYFFLTPEKGADTAIYLATAPELSEVSGQYYYRREIKELSPRAKNTEDAARLWKWSLEQTGLK
>NZ_CP009285.1|WP_042211083.1|1674717_1674897_+|hypothetical-protein
MKYKNCPAKPLEQAEILPFVQQFWSWADRMREIGNNPDLFHIPDITFRRNNRWIGKVTA
>NZ_CP009285.1|WP_042211084.1|1674872_1675376_+|N-acetyltransferase
MDWQGYSIEDAAIEDLGAIVEIYNTTVAGRMVTADLEPVAVEDRVKWFHEHNSHHRPLWVLRQGGEIAAWFSFQSFYGRPAYNGTAEISVYVNEKFRGSGAGSILLTKAVEECPRLGLQNLVGFVFGHNEPSLALLRKFGFEQWGLLPGVAVLDGIARDLVIIGRKL
>NZ_CP009285.1|WP_042211085.1|1675413_1675761_-|helix-turn-helix-transcriptional-regulator
MKSTELCPRLQKSMDIIGRRWTGLIIYQLLQGPQRFGAIEASLPVSGRLLSERLKELEQEGIVLREVFPETPVRIQYSLTDKGRALESVIRDLQVWSEDWITEEECRSESSASPQ
>NZ_CP009285.1|WP_042211086.1|1675852_1676113_+|YqkE-family-protein
MAKKKKITPAPRPAAADAPATLKDLLSRDVLDKLKAQSDALKAEEQGKKDAAIKEAEDKRKAEQKRLENDFGHLLENSSQDWSKFK
>NZ_CP009285.1|WP_042219056.1|1676255_1677329_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MYKAYTYRIYPNREQQHYLANVFGAVRFIYNKMLSDKIKHYHITATMLHTTPAGYKKEFPWLREIDSLALANVQLHLDQAYKQFFQKKTMGFPRFKSKKTHTDRFTTNNQKGTIGIEGGMLKIPKLKSRIRIRMHRPFSGRVKSCTISKTPSGKYFASIRVETESTPLPIAAQKIGVDLGLKSFAVTSEGEVIANPKHLRKSEQRLIMLQKSVSRKKKGSHNRTKAKLRMAKLHEKIANQRKDFLHKTSTRMIHENQVIVMEDLRVKNMLQNHKLAKAISEVSWRLFRELLTYKAEWYDRQLIIAPPNYASSQLCSYCGYKNAEVKNLAVREWSCPECHTEHDRDRNAAANLLKLAM
>NZ_CP009285.1|WP_174479851.1|1677827_1679246_+|RtcB-family-protein
MPRYKHEVALPGGDLKVYASEQLFGSLDYKVLEMANNNLQIPNIEYMSYTPDVHVGVGTCIGTTAVWDAASGYVSPSIVGSDIGCGMRVHLTNLHADDLRDVKLRRKLVRAIEKYLPMEAQQRGHYSDIRLENIVRKGLHGLPGKYVPDSYTPKKSSALSHVEISKLAFDEEILNELPDMAWHRGHRQLGTLGGGNHFVEIQAVEIAEEQREVAEAWGLKDGQIAVMIHSGSRAWGGMVNQFCTPAFAKVMGQLGLGSADPRLIYAPLAHPQARRYVNLMYSALNYAVVNRHLIAYGVREGFRDVFGTKCELRTLYDLMHNYAWEEETSSGTKFVHRKGATRALPAGHPDNPSAYAATGHPALIPGSMGTASYIMAGQPGGEENYYSICHGAGRIRSRTATKRLVSVHEFSQSLKVGTPDEIVVNQHSLESIIDESPQAYKNVDEIIESVTGAGLAAVVAKCKPLAAIKGTK
>NZ_CP009285.1|WP_042211088.1|1679247_1680534_+|ATP-binding-protein
MEQEIKKPTVIYEYDEDKAGIIKGYDVYARLVDGILEALYNRYGVRYELYASDDPNSEYWKLLENDVQSGNAGVEHVARIFDRLEDRTFVFDDEKEQPEYNIHLSVRNNVLAYPAMGIALARVPVFQENGINFQDYVFAASDAQLQFFLGNVRTRQREQNINKVTVFTDRRNGILREDEPITRSVGREEVVLDAGIKKEIYRSLDQFFDSDRSFYVTYDIPYKRGILLYGHPGNGKTTLVKSIAGSVPGPVLYWQITEYTSSESVNEVFEAAARLAPMVLVIEDIDSMPQEVRSFFLNTLDGATSKEGIFLIGTTNYPEKIDPGLMNRAGRFDRAYEIKMPNEALRLEYLQLRGFSAFAGEEGTATAARLTGDFSLTQLGELYVSAALEWHENGTADVESLVRGMRGELDKGRKREWMKDASSSIGFY
>NZ_CP009285.1|WP_042211089.1|1680783_1681287_+|sigma-70-family-RNA-polymerase-sigma-factor
MEPNSLDDLYENYVADIYRYLRSLCHDHHAAEDLMQETFYRAYLYLEDCREERIKPWLFRVAYNAFVDYKRKEKRSVSKEDGFFSGLPHPETTEGTLLRQERWEETALAFSRLPEVQRHALLLHDYHGLTYKEAAGIMNVGLSQYKILVFRARQKLREADRRRNEHE

Crispr_ID: NZ_CP009285_8

• CRISPR_ID: NZ_CP009285_8
• CRISPR_location: 1748933-1749021
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_8

Consensus_repeat	Method
AGAAGCGGATGTTCCGCAAAACT	CRISPRCasFinder

spacers of NZ_CP009285_8

>8.1|1748956|43|NZ_CP009285|CRISPRCasFinder
CAGCGTATGCTTTCGAAGCAGTTTTGCTGTAAAGAGAATTCTG

CRISPR arrays and Neighbor proteins around NZ_CP009285_8

CRISPR arrays

The CRISPR arrays of NZ_CP009285_8

>merge|NZ_CP009285|8|1748933-1749021|CRISPRCasFinder
AGAAGCGGATGTTCCGCAAAACTCAGCGTATGCTTTCGAAGCAGTTTTGCTGTAAAGAGAATTCTGGGAAGCGGATGTTCCGCAAAACT

>NZ_CP009285|8|7|1748933-1749021|CRISPRCasFinder
AGAAGCGGATGTTCCGCAAAACT	CAGCGTATGCTTTCGAAGCAGTTTTGCTGTAAAGAGAATTCTG
GGAAGCGGATGTTCCGCAAAACT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_099052447.1|1756136_1757681_+|leucyl-aminopeptidase	unknown	unknown	gnl|CDD|234863
NZ_CP009285.1|WP_042211133.1|1739690_1746311_+|cadherin-like-domain-containing-protein	unknown	unknown	gnl|CDD|227268
NZ_CP009285.1|WP_042211130.1|1733204_1733651_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP009285.1|WP_042134488.1|1747840_1748383_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP009285.1|WP_042211132.1|1737792_1739334_+|2-isopropylmalate-synthase	unknown	unknown	gnl|CDD|234864
NZ_CP009285.1|WP_042211129.1|1732828_1733182_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211134.1|1748379_1748844_+|zf-HC2-domain-containing-protein	unknown	unknown	gnl|CDD|379219
NZ_CP009285.1|WP_042211131.1|1734272_1736024_+|biosynthetic-type-acetolactate-synthase-large-subunit	unknown	unknown	gnl|CDD|272915
NZ_CP009285.1|WP_042211141.1|1758035_1758218_-|FeoB-associated-Cys-rich-membrane-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211137.1|1750741_1751722_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381313
NZ_CP009285.1|WP_039301477.1|1754147_1754555_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211138.1|1752057_1753140_+|3-isopropylmalate-dehydrogenase	unknown	unknown	gnl|CDD|234832
NZ_CP009285.1|WP_039301500.1|1736693_1737686_+|ketol-acid-reductoisomerase	unknown	unknown	gnl|CDD|235491
NZ_CP009285.1|WP_042211136.1|1749554_1750643_+|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|372574
NZ_CP009285.1|WP_042211135.1|1749037_1749535_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211142.1|1758261_1760274_-|ferrous-iron-transport-protein-B	unknown	unknown	gnl|CDD|223447
NZ_CP009285.1|WP_042211139.1|1753378_1753918_+|peroxiredoxin	unknown	unknown	gnl|CDD|239313
NZ_CP009285.1|WP_081971946.1|1746419_1747565_-|response-regulator	unknown	unknown	gnl|CDD|226456
NZ_CP009285.1|WP_039301592.1|1736029_1736509_+|acetolactate-synthase-small-subunit	unknown	unknown	gnl|CDD|183365
NZ_CP009285.1|WP_042211140.1|1754888_1755992_+|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|236901

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042211133.1|1739690_1746311_+|cadherin-like-domain-containing-protein	gnl|CDD|227268	COG4932, COG4932, Predicted outer membrane protein [Cell envelope biogenesis, outer membrane].	2.89728e-180
NZ_CP009285.1|WP_042211130.1|1733204_1733651_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	9.64941e-13
NZ_CP009285.1|WP_042134488.1|1747840_1748383_+|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	4.82644e-41
NZ_CP009285.1|WP_042211132.1|1737792_1739334_+|2-isopropylmalate-synthase	gnl|CDD|234864	PRK00915, PRK00915, 2-isopropylmalate synthase; Validated.	0
NZ_CP009285.1|WP_042211142.1|1758261_1760274_-|ferrous-iron-transport-protein-B	gnl|CDD|223447	COG0370, FeoB, Fe2+ transport system protein B [Inorganic ion transport and metabolism].	0
NZ_CP009285.1|WP_042211134.1|1748379_1748844_+|zf-HC2-domain-containing-protein	gnl|CDD|379219	pfam13490, zf-HC2, Putative zinc-finger. This is a putative zinc-finger found in some anti-sigma factor proteins.	7.39678e-08
NZ_CP009285.1|WP_042211131.1|1734272_1736024_+|biosynthetic-type-acetolactate-synthase-large-subunit	gnl|CDD|272915	TIGR00118, Probable_acetolactate_synthase_large_subunit, acetolactate synthase, large subunit, biosynthetic type. Two groups of proteins form acetolactate from two molecules of pyruvate. The type of acetolactate synthase described in this model also catalyzes the formation of acetohydroxybutyrate from pyruvate and 2-oxobutyrate, an early step in the branched chain amino acid biosynthesis; it is therefore also termed acetohydroxyacid synthase. In bacteria, this catalytic chain is associated with a smaller regulatory chain in an alpha2/beta2 heterotetramer. Acetolactate synthase is a thiamine pyrophosphate enzyme. In this type, FAD and Mg++ are also found. Several isozymes of this enzyme are found in E. coli K12, one of which contains a frameshift in the large subunit gene and is not expressed. [Amino acid biosynthesis, Pyruvate family].	0
NZ_CP009285.1|WP_042211137.1|1750741_1751722_-|aldo/keto-reductase	gnl|CDD|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	3.61617e-158
NZ_CP009285.1|WP_099052447.1|1756136_1757681_+|leucyl-aminopeptidase	gnl|CDD|234863	PRK00913, PRK00913, multifunctional aminopeptidase A; Provisional.	0
NZ_CP009285.1|WP_042211138.1|1752057_1753140_+|3-isopropylmalate-dehydrogenase	gnl|CDD|234832	PRK00772, PRK00772, 3-isopropylmalate dehydrogenase; Provisional.	0
NZ_CP009285.1|WP_039301500.1|1736693_1737686_+|ketol-acid-reductoisomerase	gnl|CDD|235491	PRK05479, PRK05479, ketol-acid reductoisomerase; Provisional.	0
NZ_CP009285.1|WP_042211136.1|1749554_1750643_+|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	6.89295e-11
NZ_CP009285.1|WP_042211139.1|1753378_1753918_+|peroxiredoxin	gnl|CDD|239313	cd03015, PRX_Typ2cys, Peroxiredoxin (PRX) family, Typical 2-Cys PRX subfamily; PRXs are thiol-specific antioxidant (TSA) proteins, which confer a protective role in cells through its peroxidase activity by reducing hydrogen peroxide, peroxynitrite, and organic hydroperoxides. The functional unit of typical 2-cys PRX is a homodimer. A unique intermolecular redox-active disulfide center is utilized for its activity. Upon reaction with peroxides, its peroxidatic cysteine is oxidized into a sulfenic acid intermediate which is resolved by bonding with the resolving cysteine from the other subunit of the homodimer. This intermolecular disulfide bond is then reduced by thioredoxin, tryparedoxin or AhpF. Typical 2-cys PRXs, like 1-cys PRXs, form decamers which are stabilized by reduction of the active site cysteine. Typical 2-cys PRX interacts through beta strands at one edge of the monomer (B-type interface) to form the functional homodimer, and uses an A-type interface (similar to the dimeric interface in atypical 2-cys PRX and PRX5) at the opposite end of the monomer to form the stable decameric (pentamer of dimers) structure.	2.085e-99
NZ_CP009285.1|WP_081971946.1|1746419_1747565_-|response-regulator	gnl|CDD|226456	COG3947, COG3947, Response regulator containing CheY-like receiver and SARP domains [Signal transduction mechanisms].	1.05411e-77
NZ_CP009285.1|WP_039301592.1|1736029_1736509_+|acetolactate-synthase-small-subunit	gnl|CDD|183365	PRK11895, ilvH, acetolactate synthase 3 regulatory subunit; Reviewed.	1.54966e-83
NZ_CP009285.1|WP_042211140.1|1754888_1755992_+|GHKL-domain-containing-protein	gnl|CDD|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	7.36374e-61

Protein sequences

>NZ_CP009285.1|WP_042211134.1|1748379_1748844_+|zf-HC2-domain-containing-protein
MNCATVKEWMPHYIDGQLPPEAQQTIRLHIESCPGCAEWLEEARGLAALWSEMEAGLDGLGQEAMQPMDFPDLTADVMAQIDRMENGRRERVIKATMSRRRTAPGTSWMHYGVAVGLTFLLLQFGVFEHLAYGITEINGQMSTSVSAWFGPQGK
>NZ_CP009285.1|WP_042134488.1|1747840_1748383_+|RNA-polymerase-sigma-factor
MEETEWITAVLSGEHQAFGHLVTRYQGMVYSVCIKITGEAESAKDMAQEVFIKAYKALPSFRGQSSFSTWLYRIAYRTCLDWKRANDREWRHRSTADYTENDWVTSQTPEQAALRKEASQELGENLNSLTEPYRSVVQLYYFQRHSYQEIADQKGISVKTVESQLYRARQMMRKSGEEWR
>NZ_CP009285.1|WP_081971946.1|1746419_1747565_-|response-regulator
MIRAMLVDDERLALIKLQLMLEELTPVQIIAAYTDPYEALKAAPELDPEVIFLDIDMPEMNGVQAGEMLQNLCPRAKIVFVTAYNNYAVDAFELNALDYVLKPVSRARLLKTFQRLEERIELEPDKNITDHQIMIRSLQSLRFERGGQPLSNIRWRTSKAQELFAYLFHNRNRFVSKDSLIDLLWPDFNLKKASTHLYTTIYQVRQCLKQGEIDLLINNVSGGEGYTLETGSALIDSYEWEKGILTLEPASTDNVQEHQRLLDFYTGDYLGDYDYLWAESERQRLRTIWLHHALSLAAYYIETSKIPEAVTIYQRVVRLQPYSEQGYFGLMKTYDMIGERSGVEEQYNTLTALWNGELGIGLSANITRWYEEWKQHNFRSL
>NZ_CP009285.1|WP_042211133.1|1739690_1746311_+|cadherin-like-domain-containing-protein
MKKKKWALGLGILLFVTLFAHAMGFFTNVNADANDTQITEDIVKTVTLSVYENGTQVTDNVYKLDSTVKLNLTYELPDAKYDKGATYTYTLPSQLKINQTYSGTLVNSEFADGIGTYTVGADNKVVFVFNENIEGLLDIKGTFWVESTLSSTTVTGSTTQVLYFPIAGNANNSITLQVQPSNGKAITKTGTPMPQKYNASSIDWTVDVNTLLNKLDNAVITDPMQTGLELDPASIAVYALTVDVKGNLTLGGQVSPALYDTTASDLTKLDLKFKNSINEAYRVKFTTKNISTGEQTKFNNTATLTANGSPESASAEVNINLGKTLEKFTSGYNSSDETITWEIRFNYNEKPITSNNAVLTDYFNITQDYVAGSMIIYKVKLDQNGSGTDDGTLIADTDYTLTQLPDVSGTAGFKLQFNHDIQSAYRIVYKTKVAERVYTGESIVNKATYNGQTVQASTSTTQRILNKQAVNNGTDVDYLNKTVKWTIKVNEDSRTMTNLVLTDKFTNAGLQLIGKPAISPALVEGTDYEITNLGSGEFKVNEGFVIKFLKPITKAYTITYSTKFDYYSLITASKYFINTASILWDEKTSSSAQTSSSTFTPDAKVIKNGFKTGKYDIASKKITWTVGANYNKRVLAAGAELVDTLPAGQQVVAGTVIVNKLNYGADGAHYSVNPPLVEGTDYTVTVTDKLLKVKFKDSVDYAFYVVFKTEFIDGDINLSSVTNNAILNNSEDKPVSEVLSGSASVTNGGQYVTKTGSRDSSDQTIINWTVTINANQSNVSNVQIVDTPSSNQVLLPESFQLVETTVNPANGTVNVTANKLERDKDYTLDFITDSTGKDTFKLAFTDTIDKPYILTYKSVITAVGTVPITNAVSFSGVGSQLVSKPFSFTQSFTIVDTGGTGSGVKGSLKVLKTNADQTKNLQGAEFSLGRIVGTELKDTVKATSDSAGNLEFTNLRAGKYVLKETKAPTGYALDTTARTVTINSSTPVLLTVTNDFNGSLKLTKVAQDDSSRKLAGAEFELYDATNTLVGTGTADANGVVLFTKLMGGSYTYKETKAPAGYKLNGNSVSVTIDPAQQKAVTVTNEALQGSLKLIKVDKDDAAKKLAGAKFELYNSSNTLVATSTTNASGEIVFSNLKFGTYSYQETAAPAGYELDSTKQTITIDSDVQKVLEPIKNTATLGSLKLVKVDAADSTKKLAGAKFELYNSSNAMVAAATTNASGEIIFDNLKVGAYTLEETKAPAGYDLDSTVRNITISSKVQQVLAPITNKETLGSLKLVKVDAADGTKKLAGAKFELYDSSDAVVAAATTNANGEIVFNNLKLGDYTLKETEAPTGYELDGTVRNIKIDSMVQQVLQSIPNKATTGSLKLIKVDAADGTKKLAGAKFELYNSSNTVVAAGTTNANGEIVFDDLKLGTYTLEEVKAPAGYDLDGAVRNITINSKVQQVLDPIKNKETLGSLKLVKVDYNNANKKLAGAEFKLYNSGNVLAATGVTDTNGEIVFDDLKLGDYTLEETKAPTGYDLDGAVRNVKIISDIQKVLNPIPNKETIGSIKFVKVDATDGTKKLEGAVFKLTNSSKVVVGTKTTNANGEIVFDNLKVGVYTLEETAAPAGYDLDGTPQNITINSNVQKVLDPIKNQETLGSLKLVKVDAADTAKKLAGAEFKLTNSSSGAIVTGTTNVNGELVFNDLKLGKYTLEETKAPAGYDLDESVRNITISEKAQQVLAPIKNVETLGSLKLVKVDAADTTKKLAGAEFKLTNSSNVEITKTTNASGEIVFDDLKLGSYTLEETKAPAGYELDSTPKDVTITVKAQQVLPLIKNVETLGSLKLVKVDAADATKKLKGAEFKLTNSSTNVVVTKTTNVNGEIVFEDLKLGTYTLEETKAPTGYDLDSTERTITINSKAQQILAPITNKETLGSIKLVKIAEGNAARKLAGAEFKLYDSSKNVVATAITNVNGEIEFKDLKLGVYTLQETVAPTGYYLDSTERSITIDSGVQKVLEPITNKDIPAPTGAPGTNPVVTPTPTPVSTVTPGVTSTPGPSATGVPGVTFTPGPTPIATLSPTTPAVSSAPTPQATSATTVEDIPIDGEIPLGGIPSISVEPSHGTVVVTPDGKWTYTPDPGYTGKDKFTITVTDEDGNDQDIIIEVGVDEVPTGTVTDTNSDDDGLPGDLPKTGEESPLPLYLMGGGLVVLGILLARRFKGGKKPE
>NZ_CP009285.1|WP_042211132.1|1737792_1739334_+|2-isopropylmalate-synthase
MRKIYVFDTTLRDGEQSPGVNLNTREKVEIAYQLEKLGIDRMEAGFPAASPGDLAAVNAVARAVKNVTLIGLSRSRESDIDAVKEALQGAQDPCIHIFLATSPIHRQHKLRMDKAQVLETAQSAIRYAKKYFSKLEFSLEDAGRTERDFMAEMVSMAIREGANVVNIPDTVGYLNPSEYGAIFKFLKDTVPDIERVQLSAHCHNDLGMATANTLAAIQNGADQIEGTINGIGERAGNTAIEEVALALETRSEFFDAKTSLVLSEISRTSRLVSKLTGMVVPGNKAIVGANAFAHESGIHQDGMLKEKTTYEIMTPETIGLKESKLVLGKHSGRHAFRDKLSDLGYDVSEEELNAAFVKFKDLADKKKEVSDEDILALLEEKLIDTPETFSLQTIYVTYGNEATPTAKVIINGQEPQPIVAVAEGNGSVDAIYNAIDQATGEEVTLGDYSIKAVSRGKDAQGEVHVVLSQGEIAAQGRGLSTDILEASARAYLDALNKLIEKRKTLLPADHASL
>NZ_CP009285.1|WP_039301500.1|1736693_1737686_+|ketol-acid-reductoisomerase
MAVTTYYEQDAELSVLKGKTIAVIGYGSQGHAQAQNLRDSGLQVVIGLREGKSFETAKNDGFEVLSVAEAVSRADVVQILMPDETQASVYKNEIEPNLKNGAALMFSHGFNVHFGQIVAPKDADVLLVAPKSPGHMVRRTYVEGFGVPGLIAIEQDATGNAKAIGLAYAKGIGCTRAGVIETSFREETETDLFGEQAVLCGGVSALIKAGFETLTEAGYAPEMAYFECLHEMKLIVDLVYEGGLATMRDSISNTAEYGDYVTGPRIITDETKKAMKEVLSDIQQGKFARDFILENQSGRAFLTATRRNEAAHPVEVVGSQLREMMHWIKK
>NZ_CP009285.1|WP_039301592.1|1736029_1736509_+|acetolactate-synthase-small-subunit
MRHTISVLVNDQPGVLQRVSGLFGRRGFNIESITVGQSEEIGLSRMVIVTLGDQHTLEQIEKQLYKLIDVIKVIDLGSKPMVARELALIKVKADPAERPEIMGVVETFRASVVDIGTTSLLVQVVGETQKIDAMIELLKPYGIKELSRTGVTAMIRGNA
>NZ_CP009285.1|WP_042211131.1|1734272_1736024_+|biosynthetic-type-acetolactate-synthase-large-subunit
MSAQLPEEVRSIEQLREKWKNPEVITGSEVLLRSLVLEGVDTVFGYPGGAVLYIYDALYGFDDFKHILTRHEQGAIHAADGYARASGKAGVCIATSGPGATNLVTGIATAFMDSVPLVVITGNVFSSLIGTDAFQEADITGITMPITKHSYLVRDVEDLPRIIHEAFHIANTGRKGPVLIDIPKDVSAAKTLFNPVQQQGVNLRGYNPRTVPNKLQLDKLVKAIAAAERPIIIAGGGVIYSGAHEAMYEFVKRTEIPITTTLLGLGCYPSAEDLWMGMPGMHGTYTANNAIQQCDLLINIGARFDDRVTGKLDGFAPKAKIVHIDIDPAEIGKNVSPDIPIVGDVKTVLEMLIPDVKRASNADAWRTQIAQWKLDQPLRYKDSETELKPQWVIQMINDTTKGEAIVTTDVGQHQMWAAQYYKFNHPRAWITSGGLGTMGFGFPAAIGAQMAHPERLVVSINGDGGMQMCSQELAICAINKIPVKIVVINNQVLGMVRQWQNLIYEKRYSYTDLAGSPDFVKLAEAYGVKGLRATNKEEAGAVWKEALETPGPVLVEFVVPKDENVYPMVTQGSTIDQMLMGDE
>NZ_CP009285.1|WP_042211130.1|1733204_1733651_-|GNAT-family-N-acetyltransferase
MIRYRRPKQDDTVIFDLIEKQLVPLSHLPQTIINQVRKDLPRRLGQGVTLVACPDYESDPLGFVHFMLHGDLLYIDMLAIAPGARRKRYGNMLMDRAERFALSRACRRAKVSVDTGNTAGLAFYEKLGYSVARYQPQNYCYELEKQFI
>NZ_CP009285.1|WP_042211129.1|1732828_1733182_+|hypothetical-protein
MAQPVTKKQVLKLVGKNIVAVKKDGSRVMGKLLRVSGNRLVLQRIGGKKVQTKALIPLVLFDLLAVGTAPYAYGGGGYGYGGAPYGGGYGYGPGPVPGPYGGYGPGPGYGVPPIGFF
>NZ_CP009285.1|WP_042211135.1|1749037_1749535_+|hypothetical-protein
MIKKRRWLTFLLAMVPGLGHMYLGFKKLGLEYMLGASLCIMFIPSMPTVFPFALAALWFYQLFDALQKAAWMKLSAAEHERMMFHPDSFGAPWTMGMPAPPVYPHDDVNPVWVGIGCVIAGIMLMLITVFPTLWRILNDMNIGAILLSLALIGYGLRMLKNNSKV
>NZ_CP009285.1|WP_042211136.1|1749554_1750643_+|DUF4097-family-beta-strand-repeat-protein
MGRWKIGSFTAAIGCIVLGGIVVLAQYDVITYEALGYIWPALLILFGLEMLLRLFIKSDAKSRVSGWAIVLIIVLVAASGAQTVLAGGSLSSILGNTTLVPVSGTLEVQQEIKNVKIELPDGKVKIEGVQGNTLEYEGKLELPGNTDSEAASALERKWKVTTEGDTIVMELEGDSGWLSNIQFGINVKAPYLNVSIPQNLAIEVETSDGSIEAAGLTAGIDVDTSNGTMDIHDITGGVEAHTSNGTVTVQNVQGEVELVSSNGAITLGNIDGALSAKSSNGKITVNSAVTGDWELKSSNGKIVVGLPAVTDATINADTSNGSLKGNVTWDGDDSNGTAVLGSGTHEVTLSTSNGSVTVDTAQ
>NZ_CP009285.1|WP_042211137.1|1750741_1751722_-|aldo/keto-reductase
MQYTKLGKSGMKVSRLCLGTMNFGPITDEKEAFRIMDAALDAGVNFFDTANVYGWGENSGLTETIIGRWFKQGGGRREKVVLATKVYGAMSDRLDGPNDEAGLSSYIIRRHLEASLQRLQTDHVELYQMHHIDRNVSWDELWGAFELAVSQGKIGYVGSSNFAGWDIAIAQQEAKARGFLGLVSEQHKYSLTCRLPELEVLPAAQHLGLGIIPWSPLDGGLLGRNALKKIEGSRSGGNSERVEQHKSQLEAFAELSLELGEPQDNIALAWLLANPAVTAPIIGPRTLEQFESALRSLEIVLEESVLKRLDEIFPGPGGAAPKAYAW
>NZ_CP009285.1|WP_042211138.1|1752057_1753140_+|3-isopropylmalate-dehydrogenase
MSEVKKIAVIAGDGIGPEVVAEAEKVLKRTEEVFGLAFETEHALFGGIAIDERGTPLPEDTLEICRSADAVLLGAVGGPQWDNNPKELRPETGLLGIRKALGLFSNLRPAVVFDCLKDASTLKPEVLEGTDLMVVRELTGGIYFGEKLRRQGEHGEEAVDTCVYNVTEVERIVRQAFEIAGKRRNKLASVDKANVLETSRLWREVVNRLAPEYPQVELEHVLVDNCAMQLLRRPSSFDVIVTENMFGDILSDEAAMLTGSIGMLASASLGEGSYGLYEPVHGSAPDIAGQGLANPIATILSLALMFRMTFGYEEAAAAIEAAVAEVLDAGHRTSDIAVDKSKAISTTEMGDLIVAAIRKA
>NZ_CP009285.1|WP_042211139.1|1753378_1753918_+|peroxiredoxin
MAERLVGKPAPDFFMETVTGDGKDFGKVSLSDYRGKWLVFFFYPLDFTFVCPTEITALSDAAADFAELDTEILGVSIDSIHSHKAWLTTPKDMNGLGPVNFPLASDITKKVASDYGVLIEEEGVALRGLFIIDPDGELKYQVVNHNDVGRSVEETLRVLQALQSGGLCAMNWKPGDKNL
>NZ_CP009285.1|WP_039301477.1|1754147_1754555_+|hypothetical-protein
MSFCCGASMVGTKGTLKHYRTQVHNVPLLFCPVCHRVEVHYKVENEYEILAEYAHGDGVTDVDFQDYVMEDEEAIFENVINMESEDPLAIVRSQIDMSLDLLAVAKQIGDTKWERELKKRLAVMSQRRHRLQQKA
>NZ_CP009285.1|WP_042211140.1|1754888_1755992_+|GHKL-domain-containing-protein
MISQYQESLLLPARTFQSGPMDTTYEDVLEHIDSGILLFDEEGVLTFVNKQMYGILELNRHSLLGCTLSHLLTHIQLSRFKKKLVLRSYREMVVKGKPSYEFVDEYGRYWRASLCSGEQMKGCYLFTLKEISDFKLIEQTAYQNDSLAMLGRLSASIAHEIRNPLTAIRGFIQLLHPHLHLLGKEEYAKIILAEIDRANDIIHEFLTSSKPSVPQVSMIPVSALLKEVVLLTESEALMKGCQINLQVLQEDLFISGDTKQMKQVVLNMIRNAMEAISERADDSMGRIEVGARKEGTEVRIFISDNGKGMDICTLDRLFNPFFTTKENGTGLGLSVSDRIIKNHGGCISVSSRLNEGTRFVISLPLIH
>NZ_CP009285.1|WP_099052447.1|1756136_1757681_+|leucyl-aminopeptidase
MIIEWSSGSEAASLQGDALCFIVSEAQAQGEGLPAEWAERISLLSKAGLFSGKLGQVYLLPVTGRPERPVVILAGSGNGSAGVHDLRLLMAQTARAAHRLKAAALIVQIPDEWNQLPGAVEAETAGQALAEGLVLGAYRRRHYKLEQPAYAGLNTVRLHIERQSGPSEDERWKTGILRGQAFGEATNLARDLTNLPGNLLTPSELAAAAIEVAERHSLPAEVLDEREIALKGMGGLLAVGKGSVNSPRMIAIRYQGTNHWENVVGIVGKGITFDTGGISLKRAPGMEDMISDMGGAAAVLGVMEALGRLRPRINVVMLIPSAENMPSAGAFKPGDIITSLSGRTIEVLNTDAEGRVVLGDAITYAREWGAERIIDVATLTGAVLSILGDVATGAVTNDEGFLAELMEASRLSGEQIWALPVYPEFREMLKSEVADIRNAAGRYGGASTAGLFIGEFAEGLPWIHLDIAGTAFLSKERGVNPKGATGVMVRTLLEYLFRLASDPGSQADTAGSSS
>NZ_CP009285.1|WP_042211141.1|1758035_1758218_-|FeoB-associated-Cys-rich-membrane-protein
MIVNILIVTLIFGYSGWMLYRHVQKGKEGACAGCDKGKTCSAASMDSPLSCCGSTADSKH
>NZ_CP009285.1|WP_042211142.1|1758261_1760274_-|ferrous-iron-transport-protein-B
MSSIALVGNPNTGKTSLFNTLTSSYEYVGNWAGVTVEKKVGSLKNGAGKLIDLPGIYSLHPLSRDEGVAAQYLIEETPEALINIVDASQLERNLLLTLQLLEYGKPIVLGLNMIDVANARGIQVNPEVLQAQLGITVLPLIARTGKGSSQVLSALEKPANIRPVSFQLDYGELVEEAILSITNKLQQIAGLPNLRWVSLQLMEQNPVVLELLKKRMDTSELMLICDACQTKLQQQKLALTLPQWIRSIRMDHIRSVCAAAIDATKQKPHNLTERLDSILTHRFLGLPLFIVFMYAMFKTTFDWVGGPLSDLVDGFIGGPLSDGANSLLQTIGASGFTHALIVDGIIGGVGGVLVFVPQIFILFLMISFLEDSGYMARVCLLMDSTMERMGLNGKAFIPFIIGFGCNVPAIMAARSIEQPKDRMLTTLLLPLMSCSARLPVYLLFAAVFFPAQQATAVLAMYVMGVVFALILCKLFSKHLFKNESSIFIIELPPYRMPQFKTLGRSTWEKGKGFLRKAGTIILAGSVIIWLMSYAGPSGFNVEMDNSFLAKFGGLIAPLLQPLGFGTWQAGSTLVPGFLAKEVVVSTMNIIYHAPDSAGLEGQIASVFTPLSSVSFMAFILLYIPCLATVGVIKKETASWKWTFFSMGYSLVLAYAVSLVIFQGGRLLGWS

Crispr_ID: NZ_CP009285_9

• CRISPR_ID: NZ_CP009285_9
• CRISPR_location: 2944275-2944351
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: cas3

Consensus repeat of NZ_CP009285_9

Consensus_repeat	Method
ATGTATGCGAAAAACCGAATAGAAT	CRISPRCasFinder

spacers of NZ_CP009285_9

>9.1|2944300|27|NZ_CP009285|CRISPRCasFinder
TTGCCACCAATGCAGTAAACGAGCCAG

CRISPR arrays and Neighbor proteins around NZ_CP009285_9

CRISPR arrays

The CRISPR arrays of NZ_CP009285_9

>merge|NZ_CP009285|9|2944275-2944351|CRISPRCasFinder
ATGTATGCGAAAAACCGAATAGAATTTGCCACCAATGCAGTAAACGAGCCAGATGTATGCGAAAAACCGAATACAAT

>NZ_CP009285|9|8|2944275-2944351|CRISPRCasFinder
ATGTATGCGAAAAACCGAATAGAAT	TTGCCACCAATGCAGTAAACGAGCCAG
ATGTATGCGAAAAACCGAATACAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_099052537.1|2933243_2934488_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP009285.1|WP_042211884.1|2955260_2955728_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP009285.1|WP_042219300.1|2929584_2930493_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_042211876.1|2941907_2942561_+|HD-domain-containing-protein	unknown	unknown	gnl|CDD|224336
NZ_CP009285.1|WP_042211879.1|2945894_2946599_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211888.1|2957063_2958518_-|multidrug-efflux-MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP009285.1|WP_042211877.1|2942651_2944103_+|DEAD/DEAH-box-helicase	cas3	cd09639_cas3_CAS-I	gnl|CDD|223587
NZ_CP009285.1|WP_042211880.1|2946773_2948489_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_CP009285.1|WP_042211872.1|2934511_2936329_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009285.1|WP_042211874.1|2938057_2939836_+|glycoside-hydrolase-family-2	unknown	unknown	gnl|CDD|236657
NZ_CP009285.1|WP_042211869.1|2930493_2931327_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042211878.1|2944614_2945844_+|M20-family-metallopeptidase	unknown	unknown	gnl|CDD|349944
NZ_CP009285.1|WP_042211881.1|2949051_2950284_+|MFS-transporter	unknown	unknown	gnl|CDD|340897
NZ_CP009285.1|WP_042211870.1|2931347_2933126_+|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350141
NZ_CP009285.1|WP_042211873.1|2936321_2937962_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_081972361.1|2950639_2951611_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|223687
NZ_CP009285.1|WP_052429449.1|2953351_2954638_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP009285.1|WP_042211883.1|2954634_2955264_-|LysE-family-transporter	unknown	unknown	gnl|CDD|224199
NZ_CP009285.1|WP_052429448.1|2951742_2953344_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238566
NZ_CP009285.1|WP_042211875.1|2940333_2941611_-|histidine--tRNA-ligase	unknown	unknown	gnl|CDD|237097

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_042211877.1|2942651_2944103_+|DEAD/DEAH-box-helicase	cas3	cd09639_cas3_CAS-I	5.3e-14	46.7	0.2

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_099052537.1|2933243_2934488_+|ABC-transporter-substrate-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	6.05108e-81
NZ_CP009285.1|WP_042211884.1|2955260_2955728_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	1.30433e-43
NZ_CP009285.1|WP_042219300.1|2929584_2930493_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	4.36976e-77
NZ_CP009285.1|WP_042211876.1|2941907_2942561_+|HD-domain-containing-protein	gnl|CDD|224336	COG1418, COG1418, Predicted HD superfamily hydrolase [General function prediction only].	4.06111e-33
NZ_CP009285.1|WP_042211888.1|2957063_2958518_-|multidrug-efflux-MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	7.41545e-96
NZ_CP009285.1|WP_042211877.1|2942651_2944103_+|DEAD/DEAH-box-helicase	gnl|CDD|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	5.33825e-148
NZ_CP009285.1|WP_042211880.1|2946773_2948489_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP009285.1|WP_042211872.1|2934511_2936329_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.43895e-62
NZ_CP009285.1|WP_042211874.1|2938057_2939836_+|glycoside-hydrolase-family-2	gnl|CDD|236657	PRK10150, PRK10150, beta-D-glucuronidase; Provisional.	4.44961e-47
NZ_CP009285.1|WP_042211869.1|2930493_2931327_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	9.41348e-74
NZ_CP009285.1|WP_042211878.1|2944614_2945844_+|M20-family-metallopeptidase	gnl|CDD|349944	cd08659, M20_ArgE_DapE-like, Peptidase M20 acetylornithine deacetylase/succinyl-diaminopimelate desuccinylase (ArgE/DapE)-like. Peptidase M20 acetylornithine deacetylase/succinyl-diaminopimelate desuccinylase (ArgE/DapE) like family of enzymes catalyze analogous reactions and share a common activator, the metal ion (usually Co2+ or Zn2+). ArgE catalyzes a broad range of substrates, including N-acetylornithine, alpha-N-acetylmethionine and alpha-N-formylmethionine, while DapE catalyzes the hydrolysis of N-succinyl-L,L-diaminopimelate (L,L-SDAP) to L,L-diaminopimelate and succinate. Proteins in this family are mostly bacterial and have been inferred by homology as being related to both ArgE and DapE. This family also includes N-acetyl-L-citrulline deacetylase (ACDase; acetylcitrulline deacetylase), a unique, novel enzyme found in Xanthomonas campestris, a plant pathogen, in which N-acetyl-L-ornithine is the substrate for transcarbamoylation reaction, and the product is N-acetyl-L-citrulline. Thus, in the arginine biosynthesis pathway, ACDase subsequently catalyzes the hydrolysis of N-acetyl-L-citrulline to acetate and L-citrulline.	1.17193e-109
NZ_CP009285.1|WP_042211881.1|2949051_2950284_+|MFS-transporter	gnl|CDD|340897	cd17339, MFS_NIMT_CynX_like, 2-nitroimidazole and cyanate transporters and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Escherichia coli 2-nitroimidazole transporter (NIMT) and cyanate transport protein CynX, and similar proteins. NIMT, also called YeaN, confers resistance to 2-nitroimidazole, the antibacterial and antifungal antibiotic, by mediating the active efflux of this compound. CynX is part of an active transport system that transports exogenous cyanate into E. coli cells. The NIMT/CynX-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.14605e-144
NZ_CP009285.1|WP_042211870.1|2931347_2933126_+|family-43-glycosylhydrolase	gnl|CDD|350141	cd18820, GH43_LbAraf43-like, Glycosyl hydrolase family 43 proteins similar to Lactobacillus brevis alpha-L-arabinofuranosidase LbAraf43 and Geobacillus thermoleovorans GbtXyl43B. This uncharacterized glycosyl hydrolase family 43 (GH43) subgroup belongs to a subgroup which includes enzymes with beta-xylosidase (EC 3.2.1.37), alpha-L-arabinofuranosidase (EC 3.2.1.55) and possibly bifunctional xylosidase/arabinofuranosidase activities, similar to Lactobacillus brevis alpha-L-arabinofuranosidase LbAraf43 and Geobacillus thermoleovorans IT-08 beta-xylosidase / exo-xylanase (GbtXyl43B). It belongs to the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. GH43 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. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. 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.	1.39164e-141
NZ_CP009285.1|WP_042211873.1|2936321_2937962_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.78631e-47
NZ_CP009285.1|WP_081972361.1|2950639_2951611_+|ABC-transporter-substrate-binding-protein	gnl|CDD|223687	COG0614, FepB, ABC-type Fe3+-hydroxamate transport system, periplasmic component [Inorganic ion transport and metabolism].	1.67819e-39
NZ_CP009285.1|WP_052429449.1|2953351_2954638_-|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.90042e-62
NZ_CP009285.1|WP_042211883.1|2954634_2955264_-|LysE-family-transporter	gnl|CDD|224199	COG1280, RhtB, Putative threonine efflux protein [Amino acid transport and metabolism].	5.0448e-10
NZ_CP009285.1|WP_052429448.1|2951742_2953344_+|helix-turn-helix-domain-containing-protein	gnl|CDD|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	2.4896e-31
NZ_CP009285.1|WP_042211875.1|2940333_2941611_-|histidine--tRNA-ligase	gnl|CDD|237097	PRK12420, PRK12420, histidyl-tRNA synthetase; Provisional.	0

Protein sequences

>NZ_CP009285.1|WP_042211877.1|2942651_2944103_+|DEAD/DEAH-box-helicase
MSEAQVQFSDYGLNEEIIRALEVLKYVDPTEVQRKVIPVALNAQDLIVKSQTGSGKTAAFAIPLCELVDWNENKPQALVLTPTRELAQQVREDITNIGRFKRIKAVALFGKQPFAPQKIELTQKTHVVVGTPGRVFDHIDRGTLNLSRIKYLVIDEADEMLSMGFIEQIEKIIKQLPKERVTMLFSATLPEVIKNLCRKYMTEPVDIEIEASGITTASIEHALIEVRQAAKFGLLSDLLTVENPDSCIIFCRTQEQVNALFRGMADLEYPVDKIHGGMEQDERFEVMNAFKRGQFRYLIATDVAARGIDIENITHVINYDIPLEKESYVHRTGRTARAGKSGKAITFVTPNEHKWVKEIEGYIGFTLPEMKAPSDDAVAYAKPAFDLKLGKKQVRKAGKTEVMNQDIMKLYFNGGKKKKLRAVDFVGTIAKLEGITAADIGIITIQDNVTYVDILNGKGSLVLQAMKETTVKGKLLKCHIAKK
>NZ_CP009285.1|WP_042211876.1|2941907_2942561_+|HD-domain-containing-protein
MNHTELITAAENFAKEQLGQDTTGHDWFHTNRVRNTAALIAGMEGANVVICTIAALLHDVADEKLNPSKEAGLLKVQTWLAAHLPDEAANEQIIEIIETMSFSGGGGAPMSTLEGQAVQDADRLDALGAIGITRTMVFSGAKGRPVYDPEIAPRDESLKEEYRNYSKGTAVNHFYEKLLKLKDLMNTSYGKQLAEERHQFMLIFLEQFYKEWNQGAE
>NZ_CP009285.1|WP_042211875.1|2940333_2941611_-|histidine--tRNA-ligase
MQNIKGTYDYFGREQAIRQNVRTTLQELFELYGFESMDTTLLNELELLTSKYAGGDEILREMYQLADQGGRRLGLRYDLTILFAKVIAMNPGIEFPYRRYEIGKVFRDGPVKKGRLREFLQCDADVVGIAGPQAEAELMQLAAEVFRRLEIPVVLKWNNRRFLGEILGAVGVPPEEQLSVMLTLDKLAKIGSGGVLAELTDKQLTAETVRLISELLELDNPGFGQLVERYQLDGQPGALEVLALQQLIDAIGLGAVCVFDPFLSRGLSFYTGTVYEIFDASGSYTSSLGGGGRYDAIIGKLVRRDDIEYPTVGISFGMESIMALLGERPADTADRSGVLIIPIGGYLPEALVAAAALRSAGIRTGVDTGSRKLKKTLAAASAKGIRYVIMVGECEAAEGKLRLKDMTLGSESLVTVEEAVRLTAG
>NZ_CP009285.1|WP_042211874.1|2938057_2939836_+|glycoside-hydrolase-family-2
MTNQQRTEYPRPQFMRDNWVNLNGEWEFAFDDDNVGSREQWHLGNKPLARRIQVPFAFQSSLSGIADPGFHDIVWYRRELEIPEAFEGQEILLHFGAVDYEASVWLNGILVAKHEGGHTPFHAGISAALAPAGQPNILVVKAVDYSKDVTLPRGKQYWKSDSASIFYTRTTGIWQTVWMEAVSSVYLGKVKLTPDIDRKSIEIRSFIKGALTSNGELNSDSLKLQVEITFEGQPISSDVYSVRNLEESRSITLSDFNDHGHGHWWSPEQPNLYDVTFTLLDGGKVLDQVTSYFGMRKISIESGKLCLNNRPYFMKLVLDQGYFPDGNLTPPSDEAIRRDVELTKEMGFNGARKHQKLEDPRYLYWCDKLGLLVWGEAANAYEYSEEYVRRFTQEWQESIERDYNHPSIVVWVPLNESWGVPNIAADKRQQQHAQTMYHLTKSLDATRPVVSNDGWELVTTDLFNIHDYEWRREVLEQRYSSVEQAVSRLPGNRKLAVEGFPYADQPILITEFGGVAYKKSDWDGWGYSGAENDEDFATRLRAVIQPLLLSGVVQGYCYTQLTDVEQEINGLLTYDRVPKLPLELIRAINEGK
>NZ_CP009285.1|WP_042211873.1|2936321_2937962_+|response-regulator
MPKILIVDDESVFRKGLRKMITSLEGNWEVVGEATDGYDALDKLAELSPEVLLTDIRMPRMDGIQLQQMAGGRFKDLMTVVVSGYDEFAYVQQSMRQGAKDYLMKPVERQELGRVLERLGRELAERKALPARRDEPWQVQPVLKRHVAGHLIESLLKGKTEDSDLQLLREMGFAFGHPYFICMVIKLDKHSVEKERYQRGDASLFLLYIQQVVQEMIDRHATGISFVLSDTEVVALLNIAEPQHSLSAPGTLGDLIRRQIRSLSNLTVTIGVSNPAEGLPGIPKAYNEAGIALLYRLIEGGDKLLDYAKMTERPHSGSGPLKWSWEMLEKSITGGRVASIGPIVEHMIEELCSMAESPESIHQQICKLLLYYYELSEELNVTESWLGSKDIRKVLFDVCSLSSRQELAEKCRGLLLTLTGCIAKSREVKDIDPVTAAQRYITQHYDHPLSLKEVADEVYLNPAYFSNLFKQRTGVTFIEFLTHIRIEEARKKLAFTGEKISRIAEETGFGNVRHFNRVFKNCCGLSPKEYRDSTRNVQAALIDRKD
>NZ_CP009285.1|WP_042211872.1|2934511_2936329_+|sensor-histidine-kinase
MRLKSFRGWFRNLALARKLILINVVFIVLPLGLMGYFAFARFTETTERKVGDYQLQTLKQLTLNIDTYMNELNRLTVMPYQYPKVTDYLATKRAPGEPLTLDEISGLNSFVTQVFLNGRVDILGVSLYGTGGASYVVMPESQYVTTYKLEENVSWLNKFKGHYGQPVYVATHDLSASGGNVYRAFSIVRELRSFDDGVTLGYIVIDVDPKFISEILSKVKLDAKELLYITDDSGNLVIGKDHGLPKAAPSLSPGISGEGVSHVKSEGEGLLMAHVTSEVTGWTTVGVVPVSSLMKDTEVLRTYIILIGIICVGLALLLYVFIAYRITQPLRKLSRLMRSVERGDLSMAFPVSGTDEVGMLGHSFNGMLAKLSELGYLLYETEIREKDAQIAALQSKINPHFLYNTLGSISMYAELEGSPEIITMSNNLSKLLRYSLSGRKEHVTLQDELDHVSGYMTIQQMRYEERIHFTMTIEPSLLGCEVIPLMIQPLVENAINHALDQGIGRGRISLTADCSGQVLRITVEDDGIGMNAEALEALRLHLRNTKDLGGRSGNGLLNVHRRIVLHYGDEYGLSLESMPYQGFKAVLKLPVIIHQGRAREDDGVA
>NZ_CP009285.1|WP_099052537.1|2933243_2934488_+|ABC-transporter-substrate-binding-protein
MLLVMGGCGTDEAEESPQAAAEPVTLEYWTPFSGGDNIFMTELVQQFNREHGDIRIDQINSRLDDYYSRLRTAILSGNAPDLAIIHATNLPQFVQNGYIEPLDGLAADSGLDWSQFNTKIAESTVYGGAHYAVPLDTHTLVLYYNKKYLKEAGLLDAGDKPLIGKGEQGFTEFLQQLKAELPPGVAPLALPSTRIDSVWLWWSLYNQMQGGGVFYNPEGTQAVFNNKESLQALEFVNSLYEQELIPPDINDAFKLFYDGEAAMLITGVWGTGAFEQDEQLELGVVPVPVIYDHPAVWGDSHTLAIPAKSEMSAEKRNAAMIFARWAVEHGVMWAEAGHVPSSRKVVESGAYAALKFRSDYANTANSVAYWPRNVKQWSINEEIIRQFEKMIYKEQSPEQALQKAVDSINLQLKK
>NZ_CP009285.1|WP_042211870.1|2931347_2933126_+|family-43-glycosylhydrolase
MGKISAKPRKAWTGKNSRRIIYSLAAVLLLILAGGAYLVLQYNNSGTDEVYNGHGGTFKNTLAEIDTPDPSMIYKDGYYYMTFTHNGTDIMVMKSRTMDFRQAERKVVWYPPAETAYSANLWAPELQYIRGSWYIYFAADDGNNENHRMYVLQGDSGDPLGDYTFKGQVTDDTNKWAIDGLAMEVDDELYFVWSGWEGDVNTAQNTYIAPMSDPLTISGPRVLLSEPLLPWEQAGGPPYINEGQSVLHHDGRVFIVYSGAGSWTPYYSLGLLALKPGGNPLEAADWTKAEQPLLAMDEAAGVYGPGHNSFTVSPDGSEQWIVYHATTGAADGWNNRKARAQPVSWDDGGLPVFGKPLALSTALEVPAGMGVFQAENAIRSGNRLEFPSLPSTVDSDTPLLAHYVNPGGEPAAAAVSVNAGPPSTLQLLPAGEGLTGYAYLSLPFTAGMNTVAIELPEGGAAELKAIEIPRYEGEAQTLEGNADVQDNPYASGGAAANLSGSDAALRLSNIHVPRSGTYTVSLAVLNASPDAKLEVAVNGDSTIVSTLESQERNQLSFIELELKLQSGRNEIILFDRQGSFGIDYMDIWQKSE
>NZ_CP009285.1|WP_042211869.1|2930493_2931327_+|carbohydrate-ABC-transporter-permease
MGKAKKIGLLVLAILIALFVLLPLVWMLSTAFKNDFEALSGRMNFFPQKPTLDNFVQGLSGELMNTPILRWIINSLSVGIVGTAIVLLIDSMAAFALARLPDLPLRRTLLSMFIASLMIPSVLTFLPMYIEFNTLGLINTYQALILPATAGAFGVFLLYQFFVSFPKEIEEAARIDGVNKWNLYARILLPSAVSIMMTLGIFTFMGIYNDFVWPLYATTSPEMRTITAGIAMMATGSYTQSYGKLMAMTTIAALPVLIIFIVGQKSFVKAITSSGVK
>NZ_CP009285.1|WP_042219300.1|2929584_2930493_+|sugar-ABC-transporter-permease
MEESLLKSTWTSRFTSFLFILPYLAAFGLFLLFPILYGFVISLQDFELLSAAHPFVGLRNYITIFTPGTYENSIFFRGLWTTFQFVLYSVPLLIVVGLGMAMLVNALPAKLRGLFRTFYFLPYALSASVMAVIWLMMFDTNAGFINSLLQKLGLTGIPWLTATPWVWIALVLTTLWWTIGFNMIIFVNALNEVPEDYYEAAAIDGAGAWSRFVSITLPSIRPVMLFVMITSTIASFNIYAQPFLLTRGGPGDTTKVLLINVLDQAFVRKDIGSASAMAILMALLIMMVSIVQFRLTNRKEKV
>NZ_CP009285.1|WP_042211878.1|2944614_2945844_+|M20-family-metallopeptidase
MINVRNRGFAVPFLQRLIQVNTCNPPGNEHKLSLLLQDELRELGITSSISNVEQGRSNLEAVIAGSGTRKLMFCGHLDTVSPWSAAAGSYPPHGAVIEGGRMYGRGTSDMKSGLAAMLLAAASLHQDGIRLAGDLVFLATAGEEVDSCGARLYAEQHRHDLPELDGLVIGEPTGSRVAVGHKGALWLRISLFGRSAHGSMPQLGLNAVEGMMEVIALLHRHALEWQATDPVLGSSSLSVNKITGGVQTNVVPDQCTIDVDIRTVPPLAHGPLLREIEDKLQEIQRLHPDYRYQVDQLLDRSVVYTDPGQRLITTALEIAAQQRRQGQAGGPDEEAEGDAAIDVTPVQGVPYYTDGSVLHDNGRLPVLIYGPGDHRLAHQPDEWVDIEAFLESIDFYRELAIRFLGKAEE
>NZ_CP009285.1|WP_042211879.1|2945894_2946599_-|hypothetical-protein
MKIKILIALTALIVLCSCSKGDRIKGGSEIDWVDFVKLNGHSYTGSWENVIKNPAQVSTETVGKVKFKVADVVTNPDYRTKDGDAAFLDKGTDLYRVEGFKTDEVIAAKDEQRIGGYRLYVENDYSKNLQQRYNDVIKDNIERVELYHQDDVKPYKTLDDSETKRFIHLLESGRNTQNYSPQNKEGDPVYYQVVLYTGEPFAFAFSLVDDGVNVYFSPWYTRIVGDEIRSLIEP
>NZ_CP009285.1|WP_042211880.1|2946773_2948489_-|ABC-transporter-ATP-binding-protein
MLRRFFSYYRPYKKLFILDFTCAVGAGLLELAFPVAVNKFIDDLLPGQDWPLILIACVVLLAIYALNTAMNYVVTYWGHMLGINIETNMRKKMFDHIQKLSFRFFDNNKTGHLLGRITNDLNDIGEVAHHGPEDVFIAVMTLIGAFILMADINLQLAVITFIIVPIMAWVIIHFGRNMTDTYHRLFGNVGNFNARIEDNVGGIRVVQSFANEEYEKELFAVDNQKFRQTKLMAYKLMAKSSSVSYMMTRLITIVVMVCGAWFFIQGELEIGEFVAFILLANVFFRPIEKINSVIESYPKGIAGFKRYLEVIDTEPDIADKPDAVEVGSLRGDISFSNVSFGYEADRTVLADISLKVNAGETIAFVGPSGAGKTTICSLLPRFYDVTGGAISIDGIDIRDMKLSSLRKQIGIVQQDVFLFSGTIRENIAYGKLDAELPEIWQAARQAHLEELINSLPNGMDTVIGERGVKLSGGQKQRLAIARMFLKNPPILILDEATSALDTETEAAIQQSLADLSVGRTTLVIAHRLTTIKNADRIIVVSEDGISEEGRHEELVNAGGTYSRLYQAQYNA
>NZ_CP009285.1|WP_042211881.1|2949051_2950284_+|MFS-transporter
MKFSRQKSNLAEPGLSAHNSNTASRWMLVTGIICVAAALRAPFTSVGPLLEMIRDDLGLSNTMAGAITTLPLLAFALLSPFAPQLARKVGLANILMLAMLTLSMGILVRSASGTVTLFAGTAMIGLSIAVCNVLLPGLIKGKFPHRIGLMTGIYTVSMNICAAAASGISVPLATHSGLGWRGTLALWFIVSALATLLWIPQMKSLSPSSTGAVRSSAVRVWRSPLAWQVTLFMGLQSLLYYVLIAWFSVILGERGMSSSRAGWILSLMQLAQLPFTFFVPLWAGRMKNQRLLVVITSILFIIGILGVWLGSTELMAVWAVCIGTGGGFAFGLAMMFFSLRTRTTQEASELSGMAQSAGYLLAAMGPALFGLLHDATNSWNTPLALLAAASVLLFAAGMGAGRDRYVGDRK
>NZ_CP009285.1|WP_081972361.1|2950639_2951611_+|ABC-transporter-substrate-binding-protein
MSALAACGTNNKAADGNAVQAENAGEQAAAASATPAASSNNTSEEGATRTITGEFGDVEIPVHPKRVAGIYVEDYLKALGVTPVVQWYHPSWGKQDYLNLDVPEFDISGSMEALLDKNPDLIITDGGADAAKYEQYSMIAPTYRLPESVLQDSRLMLTAIADALGIPEKGEAVLAEYDQKVADGKAKLQQALGQEKVAVIRLNVADKTFALFGVKNRFTGVLYDQFGLTPVPMAAEMTEYQSIISEEVIPALEADHIIVFPDNGDWDTAANQEAIGILDGPLWKNLPAVKNGNIYRMERSHWQSGAITANTMKLDDLLKVMVK
>NZ_CP009285.1|WP_052429448.1|2951742_2953344_+|helix-turn-helix-domain-containing-protein
MAELLQEITGRRLFYSLTNIETVSQSPSGHDPVDVYKEHTLIIVSEGQGWLKADDRQYPLEKGTGFLIEAGSLNRIRAGERGLSFYRIAFEVIHTGDSTHSGVESTCGDGLLRPGFLNCRPYSQCVLLLDSIHHSRRIAEGIEWFAAQTRFQELLLLIMQANSPAMKTMDDHEAVERSIRYMEEHFNESLSVDQLAEIAGIGRARYTQIFKEITGQIPLEHLNGLRIERAQQQLLLTKDRLHDVALAVGYSNEYYFNRRFKGTVGVTPGQYRSLHQEGVRVFAPFLEDYLLALGITPVVQYCHAQWGKQEYLGLDQVPAFDISSGDWEGLSRYMPELIMLDDGFQRWQLGECRQVAPLLRLPFHQEDWRATLRSAAAVFGRTERVQEVIAHYEQQARQAKRMLSRSIRGQTVAVVRISSYGVALYGCEELGYSASVLHEDLGLQRHGYASRLTRGQKRVNLSREELSQLTTDHLFITFDKQEGESRELLDTRLWRSLPAVRNRCVYEVDFMAWMNYGVLSHQRKIEDVLKVLA
>NZ_CP009285.1|WP_052429449.1|2953351_2954638_-|MFS-transporter
MKTDRWSASDSSQPFNCPPHTLPQSENLREVLPASRPQSPLQLAHFLTGYFISRIGDALYTFCLPLLSFRLTGSVLVMSSMFAVSVLPVILFTPFAGVILDRFSRKRLMLCADLIRMGLIALIPVMAHYGLLAIWHLYVISLLLSIVSTGYDIAVVTLIPALSGKNLTRGNAGVQTAGQLADMLGPAIAGGLASLMSITSILWLDVASFAVILYVLYRLPQEAERTRSAKPAIFAEMSQGFLWLIRSPVQLALSVQAAIGNFGYSAAYATLTYYLITKLHLTTGQMGMTYTLLAAGGVTGSLAVIYLDRHFRRGRLIPLLLLAGTCGFVLAGFNSSWLAPGIGFGLVAACNTSWSVLSASIRQEKVPPELLGRVLSFSRVVTRTAMPAGALLGGWMSGALAPGAVFLLAAGAKLIEVIIAVASPIRRL
>NZ_CP009285.1|WP_042211883.1|2954634_2955264_-|LysE-family-transporter
MIWVALLSGLSFGFIIAAPVGPMSLLCMNRTLKSGFTAGLATGAGIALADAFYALVTVASFRVVNDFTSTYAVPLRLLGSLFLGYLGLKALGPGPAKVEPVTAAVRSGNIYSLSSACLLTLANPATLLSFMALAASLGHEVSASLFLPAGIALGSFAWWLLLSGLISLISGRLSGSFSRFLSLGTAVILVLFSLYGIFSVLSAYWREQL
>NZ_CP009285.1|WP_042211884.1|2955260_2955728_-|Lrp/AsnC-family-transcriptional-regulator
MDSLDYKIISAIMNNGRITWSELAGLLGLSSPATADRVRRLEEQGVITGYTALIDAESAGYGLAALIAVSLERPEHRQGFIELVRKLPEVQECHHTAGDDDYILKLRCRGTRDLDRIISEEIKGLPGIVRTRTTIILGTVKETPHVPLPPAERTP
>NZ_CP009285.1|WP_042211888.1|2957063_2958518_-|multidrug-efflux-MFS-transporter
MKPSTTETALQGGKPFSIKPLIPVLFALIAGMLLVMLDNTIMNVAIPELENVFHTSLKTIQWAITGYTLATSMIIPLAGWFSDRFTAKRVFLVSILLFSFGSLLCALAQSPAQLIVFRIMQGLGGGMVAPIGMALSFKIAPPERRGELMGFLAMPMLIAPLLGPVLSGWLLEYVSWHWIFLINLPIGLIAIYLGMKYLPVSGKGTSAKLDIWGMALSPLAFSSLVFGVHRGGAEGWTDSYTLLPLAFGLVALSLFIIVELRQKEPLLELRSFRSFEFTKGIILAWINQIALFGSILLIPLYLQQVRGFSSLESGMMIIPQALVSFAGVMAGGRLLDKYGARIPVFSGLVLLSAALVLLSRLDSDTTIYAMTGSFALLGLGQGLTTMQLGTHVLKSAPKDLISRVTPLTTSAQQIVGSFAVAIISGLLSSNIAEHMSQAGSAAASAHTAAMIAGFHDTFLLPLSLAICGVVLSLFLRKQERGRGQ

Crispr_ID: NZ_CP009285_10

• CRISPR_ID: NZ_CP009285_10
• CRISPR_location: 2997404-2997582
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP009285_10

Consensus_repeat	Method
AATTCTTGCACAAAATACAACAATC	CRISPRCasFinder

spacers of NZ_CP009285_10

>10.1|2997429|26|NZ_CP009285|CRISPRCasFinder
GCAATGGGCAAACGTCCGAAATTCGA
>10.2|2997480|27|NZ_CP009285|CRISPRCasFinder
TGAGCTGCAGAGGGCTCGAAATGGCCA
>10.3|2997532|26|NZ_CP009285|CRISPRCasFinder
GGAGTTATGAGGTCGCTATCTGGCAG

CRISPR arrays and Neighbor proteins around NZ_CP009285_10

CRISPR arrays

The CRISPR arrays of NZ_CP009285_10

>merge|NZ_CP009285|10|2997404-2997582|CRISPRCasFinder
AATTCTTGCACAAAATACAACAATCGCAATGGGCAAACGTCCGAAATTCGAAAATCTTGCACAAAATACAACAATCTGAGCTGCAGAGGGCTCGAAATGGCCAAAATCCTGCTTTTTGTACAACAATCGGAGTTATGAGGTCGCTATCTGGCAGAAATCCTGCATTCTGTACAACAATT

>NZ_CP009285|10|9|2997404-2997582|CRISPRCasFinder
AATTCTTGCACAAAATACAACAATC	GCAATGGGCAAACGTCCGAAATTCGA
AAATCTTGCACAAAATACAACAATC	TGAGCTGCAGAGGGCTCGAAATGGCCA
AAATCCTGCTTTTTGTACAACAATC	GGAGTTATGAGGTCGCTATCTGGCAG
AAATCCTGCATTCTGTACAACAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042211974.1|3001409_3002471_+|uroporphyrinogen-decarboxylase	unknown	unknown	gnl|CDD|234644
NZ_CP009285.1|WP_042211962.1|2996157_2996409_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042211946.1|2986472_2987309_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042211972.1|2999951_3001172_-|MFS-transporter	unknown	unknown	gnl|CDD|340949
NZ_CP009285.1|WP_042211986.1|3008015_3008837_+|DUF92-domain-containing-protein	unknown	unknown	gnl|CDD|376674
NZ_CP009285.1|WP_157764020.1|2990809_2992414_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_042211944.1|2985503_2986448_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_042219314.1|3006578_3007310_+|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176506
NZ_CP009285.1|WP_042211965.1|2996880_2997120_+|DUF1450-domain-containing-protein	unknown	unknown	gnl|CDD|377806
NZ_CP009285.1|WP_042211957.1|2992521_2993874_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|378963
NZ_CP009285.1|WP_042211970.1|2999272_2999902_+|O-methyltransferase	unknown	unknown	gnl|CDD|226607
NZ_CP009285.1|WP_042211959.1|2993897_2995994_+|DUF1080-domain-containing-protein	unknown	unknown	gnl|CDD|368908
NZ_CP009285.1|WP_042211978.1|3003528_3005001_+|protoporphyrinogen-oxidase	unknown	unknown	gnl|CDD|237009
NZ_CP009285.1|WP_081972016.1|3002587_3003532_+|ferrochelatase	unknown	unknown	gnl|CDD|183526
NZ_CP009285.1|WP_039308768.1|2996535_2996838_+|heme-biosynthesis-protein-HemY	unknown	unknown	gnl|CDD|223393
NZ_CP009285.1|WP_042211948.1|2987638_2989006_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP009285.1|WP_042211980.1|3005165_3006548_+|CapA-family-protein	unknown	unknown	gnl|CDD|214858
NZ_CP009285.1|WP_042211967.1|2997962_2999096_-|class-I-SAM-dependent-RNA-methyltransferase	unknown	unknown	gnl|CDD|223194
NZ_CP009285.1|WP_042211983.1|3007387_3008011_+|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_CP009285.1|WP_042211951.1|2989086_2990832_+|histidine-kinase	unknown	unknown	gnl|CDD|225519

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042211974.1|3001409_3002471_+|uroporphyrinogen-decarboxylase	gnl|CDD|234644	PRK00115, hemE, uroporphyrinogen decarboxylase; Validated.	1.42734e-173
NZ_CP009285.1|WP_042211946.1|2986472_2987309_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.8935e-76
NZ_CP009285.1|WP_042211972.1|2999951_3001172_-|MFS-transporter	gnl|CDD|340949	cd17391, MFS_MdtG_MDR_like, Multidrug resistance protein MdtG and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli multidrug resistance protein MdtG, Streptococcus pneumoniae multidrug resistance efflux pump PmrA, and similar multidrug resistance (MDR) transporters from bacteria. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. MdtG confers resistance to fosfomycin and deoxycholate. PmrA serves as an efflux pump for various substrates and is associated with fluoroquinolone resistance. MdtG-like MDR transporters belong to the bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) 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.	3.56959e-130
NZ_CP009285.1|WP_042211986.1|3008015_3008837_+|DUF92-domain-containing-protein	gnl|CDD|376674	pfam01940, DUF92, Integral membrane protein DUF92. Members of this family have several predicted transmembrane helices. The function of these prokaryotic proteins is unknown.	1.38127e-71
NZ_CP009285.1|WP_157764020.1|2990809_2992414_+|helix-turn-helix-domain-containing-protein	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	6.78326e-29
NZ_CP009285.1|WP_042211944.1|2985503_2986448_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	9.52049e-91
NZ_CP009285.1|WP_042219314.1|3006578_3007310_+|glycerophosphodiester-phosphodiesterase	gnl|CDD|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	4.14966e-76
NZ_CP009285.1|WP_042211965.1|2996880_2997120_+|DUF1450-domain-containing-protein	gnl|CDD|377806	pfam07293, DUF1450, Protein of unknown function (DUF1450). This family consists of several hypothetical bacterial proteins of around 80 residues in length. Members of this family contain four highly conserved cysteine residues. The function of this family is unknown.	1.23832e-07
NZ_CP009285.1|WP_042211957.1|2992521_2993874_+|FAD-dependent-oxidoreductase	gnl|CDD|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	1.16758e-136
NZ_CP009285.1|WP_042211970.1|2999272_2999902_+|O-methyltransferase	gnl|CDD|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	1.85644e-46
NZ_CP009285.1|WP_042211959.1|2993897_2995994_+|DUF1080-domain-containing-protein	gnl|CDD|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	2.37132e-11
NZ_CP009285.1|WP_042211978.1|3003528_3005001_+|protoporphyrinogen-oxidase	gnl|CDD|237009	PRK11883, PRK11883, protoporphyrinogen oxidase; Reviewed.	1.35545e-171
NZ_CP009285.1|WP_081972016.1|3002587_3003532_+|ferrochelatase	gnl|CDD|183526	PRK12435, PRK12435, ferrochelatase; Provisional.	8.53953e-123
NZ_CP009285.1|WP_039308768.1|2996535_2996838_+|heme-biosynthesis-protein-HemY	gnl|CDD|223393	COG0316, sufA, Fe-S cluster assembly scaffold protein [Posttranslational modification, protein turnover, chaperones].	5.57563e-13
NZ_CP009285.1|WP_042211948.1|2987638_2989006_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	7.49969e-31
NZ_CP009285.1|WP_042211980.1|3005165_3006548_+|CapA-family-protein	gnl|CDD|214858	smart00854, PGA_cap, Bacterial capsule synthesis protein PGA_cap. This protein is a putative poly-gamma-glutamate capsule biosynthesis protein found in bacteria. Poly-gamma-glutamate is a natural polymer that may be involved in virulence and may help bacteria survive in high salt concentrations. It is a surface-associated protein.	8.76925e-94
NZ_CP009285.1|WP_042211967.1|2997962_2999096_-|class-I-SAM-dependent-RNA-methyltransferase	gnl|CDD|223194	COG0116, COG0116, Predicted N6-adenine-specific DNA methylase [DNA replication, recombination, and repair].	1.89268e-157
NZ_CP009285.1|WP_042211983.1|3007387_3008011_+|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	2.27122e-56
NZ_CP009285.1|WP_042211951.1|2989086_2990832_+|histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.87747e-39

Protein sequences

>NZ_CP009285.1|WP_042211965.1|2996880_2997120_+|DUF1450-domain-containing-protein
MANDIRLCDECNHIKMKSIVPKLLKMAPDAEIKTGCISYCGPCGKRPFVYINGRYISGPTEDEVLAKAEAFVKQPAVKK
>NZ_CP009285.1|WP_039308768.1|2996535_2996838_+|heme-biosynthesis-protein-HemY
MNVKITRNAAKVIKKTMELEGNSELKLRVAITHSHGDHAHYGLDLDTPKENDVVISTDKEIDVILDPNQPLLDGVKIDYLYFPEEGFVITNPSKGNHGDH
>NZ_CP009285.1|WP_042211962.1|2996157_2996409_+|hypothetical-protein
MKFRKLLSLKQWSHIFRSSWQYIISPNVAMGDKLLFTIPALLYWVLPDFMPFIPIDDIGVTMLLMGWFVSRMDRKYPALKSLR
>NZ_CP009285.1|WP_042211959.1|2993897_2995994_+|DUF1080-domain-containing-protein
MTRTSKRGRLPILGIVAFLLFSLISGASGPVASAAGTTYYVDSAQGSDSSSGTSEAAAWKTLGKVNSVTFSPGDRILLKAGSVWTNQYLDLQGSGFEGNPITVDRYGSGAKPLIDFGNTAVGGEGFGVRLRNVSYWEISNLEITSGPQPTDMRRNGVLVVGEGAGAGNFRHIYIRNLDIHDIFGTDRRTGGINIHARGANTATESTWDDVLIENNTVINVADTGIQTMTDAFFNSAWTHKFDAFSNVVIRGNVVEKIHRDGILVRAGAAPLIEYNKTESIGEACDVNTSIVNYLEDITVVAAQWAYYTKGAIFQYNEASDTRMLGGDGQPWDFDIEVHDSIYQYNYSYNNEGGTLLVMNNTNNNIFRYNISQNDKDANGVFHLVNGGGNLYVYNNIIYRSGTQNKALTHASNTGMVYYTNNIFYNAASGQYTNSPRMTYDHNSFYGLNSGVPSDPNKITGNPGFFSPGTATGLASADGYKLAQTSPLINAGAVVAGNGGLDYFGNPLYNGVPDIGVFEFQGTITPPVTLFQDDFEDNNYSGWTTSGGAWSVEDDGTKALTQTSMSGEALAYTGDASWTNYTYSAKVKLLNAFGNAGLLFRYADASNYYMFRLNDSGDKAELYKKTAGTLTMVSSANVAVTPGQWTELKVTVSGSTVTAFAGGTQLIQWADTAVQPAGGKIGIRMHSSTARIDDVKVTE
>NZ_CP009285.1|WP_042211957.1|2992521_2993874_+|FAD-dependent-oxidoreductase
MNRTVFTLPAEEIAISREVDVLVAGGGPAGVAAAISAARSGARTLLIEQRGFLGGMGTVALVPAFCPYSDGEKAVVRGIGLELLEQMKAECEPEFRERFGAELDWVPIDPEVLKRVYDDAVAESGAGVLLHTIASQTVMDETGRNVKGVVIVNKSGRSLIKAKTVIDTTGDADLAALAGAPFHKGGEAGELQAATMCYLLANVDRKRFLDYLNESGDTEQIHRAVQQAQADGKLPQGRDSVSGLSWVADYLVGVNFGHVFGIDGSRAEDLTRGAIEGRKLVLRQLEFFRAYVPGFEHAHLVSSGEQIGIRETRRIVGDYVLTQDDFMNMASFPDDIARNSYFIDIHMARSSGAMHIHHLPPGKSHGVPYRCMLPVGLDNVWVAGRAASSDRVVQGSLRVMPNCFAMGQAAGMAAAIAAGSDSQSRKVDITELQRGLVQQGAWLGEALAAL
>NZ_CP009285.1|WP_157764020.1|2990809_2992414_+|helix-turn-helix-domain-containing-protein
MMTLMLIDDDVPMLEYVEYLLGSLGLELQLVASAFSSEDALEQFHSVLPDVVIIDIGLPGMDGLELADAFRITKPEVRLIFLTCYEDFHYSKRAIQLEADDYLIKDELSPEQLKSSLSKAMSRFKSREELLERYSFRQAIERNKEVLKQSFLKQLLSGAADQENTLEFGQRLGISWKHPYLRHGFIHMDAASVTERYRYKDIPLIHFAVNNIALELSAGEASITPIMSRDADIYLVWNVADPDCPGTGLTDFMQSVLDKVAQYLKITLRGFYSGASAPLRNFDALHKTLMESRDHNFYQAVTPIAALEEQANFGQTAEWRGDKERGMLSLALEEGQAAWIDLAVNQWTQQVTADRLLPRLVKEACGNFVRQMAFEAGGLAEEDFFTQLEQTVHIREAAGLTKRELRNLWRQHTLAPVAAEEKDIRLQEVDRFLEEHVDQMVTSTDMAEHLHLNASYFSRYFKKLSGINFTDYVNQYKMNMAITMLARPHETVENVAYTLGFSDRAYFSKVFKKYSGRNPSEYKAGPVEESGAEE
>NZ_CP009285.1|WP_042211951.1|2989086_2990832_+|histidine-kinase
MKWLSRFSFHRRLQFTFLILILLPFIVVTFWSYTSVRENVSDKITRAGEETLKVIGSQIEKTVDSISFVSVYFSEAYDPAVLESLRYLKNTGNFGNYGVYTHYNKLKTTANILSVQSLDADLQIMLVNRENRILIGNQNIPVFSGLPEQLLLESSKLNEQEKISLQWFPYGGDPSAPDYYYAVRFITDPLNQEKLATLYVGIPSHYFHNLLDTGNSANILSLADGMGRSIAVTGGADIPKESQMLVSEVRIPKVGWLLTSKTPRSSIDSHINREFLVSISIVGLFFLAFLILSMLWAGYINKPISLLRASVKQYVGGNRAVRIPVRGKDEVAVLSSAFNQMLDDMNQLLQQVESEQEEKRLLELQALAAQIRPHFLLNTLNSIKVDLLLSGDQPHGAMIDALMKLLRVYVHVDKPLELAEECKVLGSYVQVMQIRNRLDIAFECVLDEKVGEVMLPRLLLQPIVENAISHGFSARPAKPAIRLEAAFEDDMLKISISDNGRGMPEDKLQRLNRRLQGNEDTALWPEKGVGLVNTARRLQVLYGYRARLMAQAGTEEGMIFTLFIPVTSEKEAVPLDDPDAD
>NZ_CP009285.1|WP_042211948.1|2987638_2989006_+|extracellular-solute-binding-protein
MKKLSLVLASMILMLTVTACGGNGNSNNSAATDAPASADPAAGSSSTDQPAGKAKIKFYTFKADKPEEPIYQAVQAYNESQDKVEVEYESLVQNSDSTDFMKKLDILVAGGEVVDVFMTGNEDELLERASRGVVEPLNSFFEQESITPEDEYSKLLKLDDKVYGILPSSTQWLTVFNKDHLEAAGLSLPEMGWTWDDFRDYAKKLTTPEHFGTYFHTWGEYPNIIAYTEKPHPQLSADLKPIFDDPSFEYFFNLRRTMEKEDKSVEPYADVLASNYHVLQQFFAGNASMLAVPSYAVRAALNLEKFPHEFQTMYAPLPRSVDTEELGMTNISGGGLAMGAKSENKEASYDFIRWMSKESYKFTKEIPAFKGVDGAELINGFFGENTDLIDTASLSKTLFDPNIQMPDTFSVPYGSELKAIVENGFASFILDNRSFDEVKVEMTAEVEKVVQANQK
>NZ_CP009285.1|WP_042211946.1|2986472_2987309_+|carbohydrate-ABC-transporter-permease
MTMRKFKTGNLIFTALFALLSVFFLMPLVWMLSAASKTEKEVWTFPIQWIPTDWNLVANFKAVWMGDVAFGLFYMNSIKIALISTIATIVISAMAGYALGKLDFKGRTLIFTLMLAFMMIPEQATLVPRYIMIKELGLYDSHAALILMGMFSSYFTFLLRQFMIGIHNDMLEAAELDGAGFFRIFWSVVLPLSRPILATVGIIKFIWTWNDYQGPLIMLNSTKLYTIPLGMQFFKEEFGTQISVMMMASVAAILPLLALFLALQKQVIDGIAIGGVKG
>NZ_CP009285.1|WP_042211944.1|2985503_2986448_+|sugar-ABC-transporter-permease
MSESAVTRKTTTAGAPSKTYWTRKRREQLAGWIFIAPEVIGMLVIAVFPLLFSLFLSLTEWNLVGGLSAIHFVGLDNFIELFRDNRFLLALKNNVLFTVGTVPVTMLLGVVLSALIHKKLYAKSFFKVAFFVPYICSTVAIAAVWQALYHPSKGPINQILMQIGLSEPPRWLVDTSFSLIAIMIIYIWQLLGYQIIIFLAGMTNIPEELYEAATIDGASGIGQFRRITLPLLGPTTFFLAITSTISSFKIFDMIKFLTDGGPNYSSTVIVYQIYEEGFERFKMGYASAMSWVLFLIIMLVTSITWMTQNRKVHY
>NZ_CP009285.1|WP_042211967.1|2997962_2999096_-|class-I-SAM-dependent-RNA-methyltransferase
MGKLQLIATAPMGLEAVVARELNELGYETTVENGRVLFSGDYIDICRCNLWLRTSDRVLVKMGQFPAKTFDELFEGVKAINWEDWIPENGEFPVEGRSHKSQLTSVPACQGIVKKAIVEKLKLSYHTEWFPENGPRYVVEVILLNDIALITLDTTGPALHKRGYRRQATEAPLKETMAAALIQLSRWNGHRPLYDPCCGSGTILIEAAMIAWNIAPGLRRSFPSEHWPEIPQRLWEEAREEAFDAVRDDYPLQLTGTDIDPVAIEIAEAAAKSAGLSGEITFKHMAAAKARPEGEYGCIITNPPYGERISNDKEVEKLTRQFGEMMLYLPTWSFFAISPYKEFEQYYGRKADKRRKLYNGRIECQYYQYLGPLPPRN
>NZ_CP009285.1|WP_042211970.1|2999272_2999902_+|O-methyltransferase
MQNQEEYSEQLYTEDELLLKVKQAIVANGMPEVSIAPGYGRLLTMLVTLSRSTRILEIGALGGYSGICLCRGLTQSGSLTSLELKADYAKLAHSHLEQAGFGDAVEYKIGPALDSLKLLEAQGQKFDFFFIDADKENYPNYLEYAIRLASPGAIIAGDNIFLRGRTLNTEKNGPAVQAMRRFNEMIASDPRLTSTLLPAYDGLALAMVK
>NZ_CP009285.1|WP_042211972.1|2999951_3001172_-|MFS-transporter
MKNWETWKVNLMVLWFGQFLVNAGMTMITPFLSLYLAKDLGVTGDHAIGMWAGLIFAANFLTSFIFQPLWGKLADKYGRKIMLLRSSFGMAIVIVLMGFAQSPMQLLLLRLLNGTISGFNPASIALVSGTTPKPRMGFAMGLMQSGAVAGTILGPLIGGLLADWIGFRPIFYVVGALLFVASLLALFLVKEKFDRVEAAQVPQVSVLEGFKELAKVPQLPALFGVTFLLQFAMISPMSLLPIYVEKLHGSAVNIAFWAGMVSAVTGISNMLASPLLGKLSDKVGAHRILTYALIGAALFLIPQAFVTSVWQLILVRFLMGVFMGGLLPSVNALIRSYTPDGKESRAFGFNSSTLALGNMLGAVIGGFLSGYIGIEGLFIISGAFLLINTVWVRLKLYKKTEPRLFR
>NZ_CP009285.1|WP_042211974.1|3001409_3002471_+|uroporphyrinogen-decarboxylase
MTYNDTFIRACRQQSTEHVPVWYMRQAGRYDPEYRKIKEKYSLLEICRQPELAAEVTLMPVRKLGVDAAILYSDIMNPVASLGVNFDIVKNIGPVIENPIRSAADVDRLKPIDVEGDLGHILETIALLDKELDVPLITFAGAPFTIASYLIEGRPSKSYHRTKEMMFSQPRVWEKLMEKLGDMVIAYLRAHVASGGKAFQLFDSWVGALAPRDFEAYVLPTITRIFAGLSDLDVPKIYFPGVSSGELLPSLAKLQADVIGLDWRVSLTEGRRRTGGRFAIQGNLDPYLLTAPMDVLKERAKELIDEGITQPGYIFNLGHGLFPEASLDTLKELTDYVHEYSAAALKQAAGPLA
>NZ_CP009285.1|WP_081972016.1|3002587_3003532_+|ferrochelatase
MTTKIGVLVMSYGTPESLEDVEAYYTHIRRGNAPSAEQLKELKDRYEAIVGGVFPLRENTDRQVEALQAKLNSGQIQYVCYQGLKHARPFIEDGVEAMARDGITQAIGIVLAPHYSVMSVGTYIKRAKEKADACGIHMEFVESYHMHPELIDVLSRRVTAKLDEFEETGAARDEVRVLFSAHSLPERILAMGDPYRDQLLETSKAIADQAGVESWQFTWQSAGRTAEPWLGPDILDTLRELAETQVKYVLSAPIGFVSDHLEVLYDLDIEAQALASELDLRLLRIDSLNSDPAYMSVLSDVVRTKAGQLKVKQS
>NZ_CP009285.1|WP_042211978.1|3003528_3005001_+|protoporphyrinogen-oxidase
MSGTPRKIVIIGGGLSGLSAAYYVRKFYREAGVLPEIILIEKDKCLGGKIETLHRDGFVIEKGPDSFLARKTAMVDLARELELDHELVTTNPNAKKTYILQRGKLHPMPAGLVLGIPTELKPFLKSGLVSFGGKMRAMMDFVLPPRRSSEDESLGDLIERRLGTEVLENMTEPLLAGIYAGDMRKISLQATFPQFGEVERQYGSLIRGMTTGRKPAETHTGTKKSAFLTFRQGLQSLVHALIHDLHDVEQRTGTGAVVIKIRSSAGISAEASAAPRYEVELDNGELLQADDVYVTVQNFAAAELLRPHVDVSALDAVNYVSVANVVMAFTKKDIVTEYDGSGFLVPRKEGRNITACTWTSTKWLHTSPDDKVLLRCYVGRSGDEQNVDLPDEALAELVRKDLKEIMGITATPLFTEITRLRSSMPQYPVGHPGRIAGLRSELAQKLPGVYAFGAGYDGIGMPDCIKQAKFTAETAAAHLEKRPERAAVTV
>NZ_CP009285.1|WP_042211980.1|3005165_3006548_+|CapA-family-protein
MYPPRSRNRQSKKRSSKKKRRTVWAWFNVVLLLMITGLLAYSFMDDKDKESSAPPAVVAEPSPSPEASATAAAPTEEAPAAEATASPEPTPEATPEATPVPVETAEPVSTPARADDVAATDEPQGPTAGNAGGQLSGLPENFSGGTVKLNFAGDIIFSGKVGELLQKKGYDYSYSALDGMFKKDDLTVVNLETPITTGGVGAANKQFVFKGAPEALDALKSAGVDAVNLANNHTLDQGEEGLLDTLKHLSKRGIPYVGAGSNSKEAYSAQYFERQGIKIALLGFTRVMPVIEWKAEAGKPGLASVYDSAEALKAIAAAKKQADLVVVVVHWGKERMEQYDQTQQTLGHSFIDAGADLVMGGHPHVLQGIEPYKGKWIAYSTGNFIFTRSTLPATWETAVFQAECSKKGQCSLKLSPMDAELGQPVPMNEADGQLLLHKVESLSSGLVKIGNDGTVVQSAR
>NZ_CP009285.1|WP_042219314.1|3006578_3007310_+|glycerophosphodiester-phosphodiesterase
MNNMCVAHRGFSGKAPENTLAAVRMAIALPFVRWMEIDVQLTKDGVPVVIHDYSLDRTTNGHGKVKNMDYEHMRRLDAGSWKGRAFRGERVPSLEEVLSLASGRLRLNIELKTSGDMYPGLEKAVIDLVNTMGMREDVVLTSFDAGALQRIKELDPRFRTGLIYDSRSGDPAKKLNELGCSFLSISSDRLSPVLAKSLAERGVKIMAWTVNKGKEMRRVSAMHSDIMICTNRPDIWGDIFLQA
>NZ_CP009285.1|WP_042211983.1|3007387_3008011_+|fumarylacetoacetate-hydrolase-family-protein
MSAMVNNVYCVGRNYKLHAEELGNQVPAEPLIFLKPSHAAVALDKAIIHLPKDAGLIHYEGELVLRIARDYVPGMSVEELVDVMALGLDFTLRDVHNDLQKKGLPWTPAKGFKNAAPLTPYIAFPEQEELEATDFTVRKNGIEVQRGNVQNMIFSLQKIIEFIASRYGLGKDDIIFTGTPAGVGPVVSGDSFELFWGDTLMGTCLIG
>NZ_CP009285.1|WP_042211986.1|3008015_3008837_+|DUF92-domain-containing-protein
MLSGLEVLQWLIGASGALLVAGAAYWKQSLSFSGMLAAIVMGTIYFGAGNAFWFGILLLFFISSSLLSKLHHENKAELEATYDKTGRRDAGQVFANGGLGMLLVLLNAIYPLEIWGFLFIGVMATVTSDTWATEIGTLAKRPPRSVLTGKVLQAGTSGGVSLPGTLAAAAGGVLIGVASWLLRAASGMPQHSLLTLALAGLLGGLAGAFADSVLGATVQRMNRCAVCGREVEASMHCGKPTVYARGWRWMDNDTVNAVSSIIGGVVALLASYI

Crispr_ID: NZ_CP009285_11

• CRISPR_ID: NZ_CP009285_11
• CRISPR_location: 4621111-4621199
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_11

Consensus_repeat	Method
AAGGTGAATAGGCTCACAAAACTT	CRISPRCasFinder

spacers of NZ_CP009285_11

>11.1|4621135|41|NZ_CP009285|CRISPRCasFinder
AAGCGTATGCTTTCGAAGCGAGTTATGTACGATGTATTTTC

CRISPR arrays and Neighbor proteins around NZ_CP009285_11

CRISPR arrays

The CRISPR arrays of NZ_CP009285_11

>merge|NZ_CP009285|11|4621111-4621199|CRISPRCasFinder
AAGGTGAATAGGCTCACAAAACTTAAGCGTATGCTTTCGAAGCGAGTTATGTACGATGTATTTTCAAGGTGAATAGGCTCACAAAACTT

>NZ_CP009285|11|10|4621111-4621199|CRISPRCasFinder
AAGGTGAATAGGCTCACAAAACTT	AAGCGTATGCTTTCGAAGCGAGTTATGTACGATGTATTTTC
AAGGTGAATAGGCTCACAAAACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042214421.1|4627091_4628315_+|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl|CDD|179997
NZ_CP009285.1|WP_081972122.1|4613731_4614409_-|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl|CDD|270620
NZ_CP009285.1|WP_052429563.1|4628407_4629493_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP009285.1|WP_042214419.1|4624954_4626874_-|1,4-alpha-glucan-branching-protein-GlgB	unknown	unknown	gnl|CDD|235445
NZ_CP009285.1|WP_039299112.1|4630892_4631591_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP009285.1|WP_099052548.1|4612817_4613627_+|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl|CDD|213022
NZ_CP009285.1|WP_042214405.1|4614798_4616919_+|polyphosphate-kinase-1	unknown	unknown	gnl|CDD|235469
NZ_CP009285.1|WP_042214407.1|4616866_4618393_-|Ppx/GppA-family-phosphatase	unknown	unknown	gnl|CDD|223326
NZ_CP009285.1|WP_042214415.1|4621214_4622960_+|alpha-glycosidase	unknown	unknown	gnl|CDD|200477
NZ_CP009285.1|WP_042214399.1|4611534_4612575_-|NADH:flavin-oxidoreductase/NADH-oxidase	unknown	unknown	gnl|CDD|239242
NZ_CP009285.1|WP_039299118.1|4632906_4633632_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|226164
NZ_CP009285.1|WP_042214411.1|4619229_4619889_-|amino-acid-ABC-transporter-permease	unknown	unknown	gnl|CDD|223836
NZ_CP009285.1|WP_042214424.1|4629489_4630896_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP009285.1|WP_052429562.1|4623049_4623421_+|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl|CDD|378915
NZ_CP009285.1|WP_042214397.1|4609818_4610751_-|dihydroorotate-dehydrogenase	unknown	unknown	gnl|CDD|235982
NZ_CP009285.1|WP_042214410.1|4618520_4619243_-|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224051
NZ_CP009285.1|WP_174479822.1|4631583_4632870_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042214417.1|4623483_4624929_-|glycogen-synthase-GlgA	unknown	unknown	gnl|CDD|234809
NZ_CP009285.1|WP_042214413.1|4620024_4620840_-|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|270338
NZ_CP009285.1|WP_042137793.1|4610743_4611448_-|dihydroorotate-dehydrogenase-electron-transfer-subunit	unknown	unknown	gnl|CDD|99814

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042214421.1|4627091_4628315_+|glucose-1-phosphate-adenylyltransferase	gnl|CDD|179997	PRK05293, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_CP009285.1|WP_081972122.1|4613731_4614409_-|LysM-peptidoglycan-binding-domain-containing-protein	gnl|CDD|270620	cd14667, 3D_containing_proteins, Non-mltA associated 3D domain containing proteins, named for 3 conserved aspartate residues. This family contains the 3D domain, named for its 3 conserved aspartates, including similar uncharacterized proteins. These proteins contain the critical active site aspartate of mltA-like lytic transglycosylases where the 3D domain forms a larger domain with the N-terminal region. This domain is also found in conjunction with numerous other domains such as the Escherichia coli MltA, a membrane-bound lytic transglycosylase comprised of 2 domains separated by a large groove, where the peptidoglycan strand binds. Domain A is made up of an N-terminal and a C-terminal portion, corresponding to the 3D domain and Domain B is inserted within the linear sequence of domain A. MltA is distinct from other bacterial LTs, which are similar to each other. Escherichia coli peptidoglycan lytic transglycosylase (LT) initiates cell wall recycling in response to damage, during bacterial fission, and cleaves peptidoglycan (PG) to create functional spaces in its wall. PG chains (also known as murein), the major components of the bacterial cell wall, are comprised of alternating beta-1-4-linked N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), and lytic transglycosylases cleave this beta-1-4 bond.	5.02305e-26
NZ_CP009285.1|WP_052429563.1|4628407_4629493_-|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	2.51163e-26
NZ_CP009285.1|WP_042214419.1|4624954_4626874_-|1,4-alpha-glucan-branching-protein-GlgB	gnl|CDD|235445	PRK05402, PRK05402, 1,4-alpha-glucan branching protein GlgB.	0
NZ_CP009285.1|WP_039299112.1|4630892_4631591_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	6.32746e-82
NZ_CP009285.1|WP_099052548.1|4612817_4613627_+|polysaccharide-deacetylase-family-protein	gnl|CDD|213022	cd10917, CE4_NodB_like_6s_7s, Catalytic NodB homology domain of rhizobial NodB-like proteins. This family belongs to the large and functionally diverse carbohydrate esterase 4 (CE4) superfamily, whose members show strong sequence similarity with some variability due to their distinct carbohydrate substrates. It includes many rhizobial NodB chitooligosaccharide N-deacetylase (EC 3.5.1.-)-like proteins, mainly from bacteria and eukaryotes, such as chitin deacetylases (EC 3.5.1.41), bacterial peptidoglycan N-acetylglucosamine deacetylases (EC 3.5.1.-), and acetylxylan esterases (EC 3.1.1.72), which catalyze the N- or O-deacetylation of substrates such as acetylated chitin, peptidoglycan, and acetylated xylan. All members of this family contain a catalytic NodB homology domain with the same overall topology and a deformed (beta/alpha)8 barrel fold with 6- or 7 strands. Their catalytic activity is dependent on the presence of a divalent cation, preferably cobalt or zinc, and they employ a conserved His-His-Asp zinc-binding triad closely associated with the conserved catalytic base (aspartic acid) and acid (histidine) to carry out acid/base catalysis. Several family members show diversity both in metal ion specificities and in the residues that coordinate the metal.	1.86563e-80
NZ_CP009285.1|WP_042214405.1|4614798_4616919_+|polyphosphate-kinase-1	gnl|CDD|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP009285.1|WP_042214407.1|4616866_4618393_-|Ppx/GppA-family-phosphatase	gnl|CDD|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	8.38522e-92
NZ_CP009285.1|WP_042214415.1|4621214_4622960_+|alpha-glycosidase	gnl|CDD|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_CP009285.1|WP_042214399.1|4611534_4612575_-|NADH:flavin-oxidoreductase/NADH-oxidase	gnl|CDD|239242	cd02932, OYE_YqiM_FMN, Old yellow enzyme (OYE) YqjM-like FMN binding domain. YqjM is involved in the oxidative stress response of Bacillus subtilis. Like the other OYE members, each monomer of YqjM contains FMN as a non-covalently bound cofactor and uses NADPH as a reducing agent. The YqjM enzyme exists as a homotetramer that is assembled as a dimer of catalytically dependent dimers, while other OYE members exist only as monomers or dimers. Moreover, the protein displays a shared active site architecture where an arginine finger at the COOH terminus of one monomer extends into the active site of the adjacent monomer and is directly involved in substrate recognition. Another remarkable difference in the binding of the ligand in YqjM is represented by the contribution of the NH2-terminal tyrosine instead of a COOH-terminal tyrosine in OYE and its homologs.	4.16941e-163
NZ_CP009285.1|WP_039299118.1|4632906_4633632_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|226164	COG3638, COG3638, ABC-type phosphate/phosphonate transport system, ATPase component [Inorganic ion transport and metabolism].	2.70602e-71
NZ_CP009285.1|WP_042214411.1|4619229_4619889_-|amino-acid-ABC-transporter-permease	gnl|CDD|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	8.95367e-84
NZ_CP009285.1|WP_042214424.1|4629489_4630896_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.10321e-61
NZ_CP009285.1|WP_052429562.1|4623049_4623421_+|nuclear-transport-factor-2-family-protein	gnl|CDD|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	1.50391e-06
NZ_CP009285.1|WP_042214397.1|4609818_4610751_-|dihydroorotate-dehydrogenase	gnl|CDD|235982	PRK07259, PRK07259, dihydroorotate dehydrogenase.	3.90699e-150
NZ_CP009285.1|WP_042214410.1|4618520_4619243_-|amino-acid-ABC-transporter-ATP-binding-protein	gnl|CDD|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	1.74895e-162
NZ_CP009285.1|WP_042214417.1|4623483_4624929_-|glycogen-synthase-GlgA	gnl|CDD|234809	PRK00654, glgA, glycogen synthase GlgA.	0
NZ_CP009285.1|WP_042214413.1|4620024_4620840_-|transporter-substrate-binding-domain-containing-protein	gnl|CDD|270338	cd13620, PBP2_GltS, Substrate binding domain of glutamate or arginine ABC transporter, a member of the type 2 periplasmic binding fold protein superfamily. This family comprises of the periplasmic-binding protein component (GltS) of an ABC transporter specific for glutamate or arginine from Lactococcus lactis, as well as its closely related proteins. The GltS domain belongs to the type 2 periplasmic binding protein fold superfamily (PBP2), whose many members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.64684e-87
NZ_CP009285.1|WP_042137793.1|4610743_4611448_-|dihydroorotate-dehydrogenase-electron-transfer-subunit	gnl|CDD|99814	cd06218, DHOD_e_trans, FAD/NAD binding domain in the electron transfer subunit of dihydroorotate dehydrogenase. Dihydroorotate dehydrogenases (DHODs) catalyze the only redox reaction in pyrimidine de novo biosynthesis. They catalyze the oxidation of (S)-dihydroorotate to orotate coupled with the reduction of NAD+. In L. lactis, DHOD B (encoded by pyrDa) is co-expressed with pyrK and both gene products are required for full activity, as well as 3 cofactors: FMN, FAD, and an [2Fe-2S] cluster.	7.42783e-79

Protein sequences

>NZ_CP009285.1|WP_042214413.1|4620024_4620840_-|transporter-substrate-binding-domain-containing-protein
MNKWGKLSMGLLLAAGLLAGCGSNNNDNNTAASGNANTGTEAKTLIMGTSADFPPYEFHKMVDGKDTIVGFDIEIAKEIAADMGAKLEVKDLPFDSLLNELSSGRIDMVISGLSPTPERAEAVGLSEIYYKAEQAVVVREADKDKFATMDSLKGAKLGIQTGSIQEDIAKGIEGAQLTSLGKISEIVLQLQSNRVDASIMEGPVAKSFVKNVKGLVITDAKPEVEDDGYVIGVKKDNTELLEQVNTTLKRLDSEGKIDEFVAAASELAESN
>NZ_CP009285.1|WP_042214411.1|4619229_4619889_-|amino-acid-ABC-transporter-permease
MSVFELAYDYRNFFLSGLKYTLLLAVMGVFFGFVLGIAVSLLRMSKWRILRFIATAWVEFLRGTPMLVQLFLIHYGLPEFGISLSPIQSGAITLTINSSAYLAEIFRAGIQGVDRGQMEAARSLGMKQGMTMRYIILPQALKNVLPAIGNEFITIIKESSIVSMIGVADLLFEARTITTITYEGLSPLVVIAVMYFVLTFTLSKLLGILERRLNTDDRG
>NZ_CP009285.1|WP_042214410.1|4618520_4619243_-|amino-acid-ABC-transporter-ATP-binding-protein
MIEVKNLQKSFGKLEILKGIDLNIHKGEVVVVIGPSGSGKSTFLRCLNLLEQPTGGEITFEGQSITAKKHDINVTREKMGMVFQQFNLFPHKSVLQNIMLAPLKVRKQQASEAEKIAMELLRTVGLEDKRDAYPAQLSGGQKQRIAIARALAMQPHVMLFDEPTSALDPEMVGEVLEVMKQLAVNGMTMVIVTHEMGFAREVGDRILFMDGGVIVEQGTPDQVFGNPKHARTRDFLSKVL
>NZ_CP009285.1|WP_042214407.1|4616866_4618393_-|Ppx/GppA-family-phosphatase
MRDDLCRIGIIDIGSNSIRLVIYDTTQAGGYKIIKECKYSARLSEKITKEGRLEKKDMDTIIPVLHQFKEICDDFEVDQIRAGATAAIRNAANSAEIIDYLSEASSIRIEVISGHQEAYFGFLGVINAFDIQDGFVIDIGGGSTEVTLFRGRRYQHSISFPFGAVNTNLMFSHGGNWNADQIRKLQLYVTGRLVEHDWLTTGTGLPLYGLGGTLRSLGKLDQKNRDYSLPNSHGYVLEGDTIGRFMETLPATPYEKRKDLDGLSKSRGDIIVSGLIIFHTVYHYIGASRAVISGEGLREGMLHDLLKPEQPVRDSALEYSLDTIIRFDIRTSKRHLDHIYKLALSLLGAFEREGDREEHEMLIYVAIMLHRTGSNINYYQSKRHTRYWLMNSPIRGLTHRQLILSAYIASYSTKSRKQKLSQMHKDILLASDEEWIHKLGTLVQLSIALDSTEIGIVSGVNARLHNNTLDLELQGGQVLIGLEDIENALKAFRNAWSVKVKLGLPSSG
>NZ_CP009285.1|WP_042214405.1|4614798_4616919_+|polyphosphate-kinase-1
MNVNAEEKKNNHTSPATAYLNRDLSWIEFNRRVLAEAQDPENPLMERAKFLAIVSSNLDEFISVRVAGIQDQIRAGYTKKDFTGYTPSGLYKRLIKRVTKIIADQYRTFKDISRSLHKEGIVFVDYKDLTHAQEQSIEQYYRDIIYPVLTPMAVDQSRPFPLVHSQFIYLAVVLTRKNSQEEEPYFAILQIPSNLPRCIPLPHRSNSKKRQFVFIEDVIRQHIQTLFSGYDPVAVSEFRLTRNSDLTIDEEGAEDLLEEIEKELRKRRRGVPARLEVQKGIHPYALEQLQAEFELEDFVFEIEGPLDLSFLRGFAGSVKGFSYLHHAPIEPLYPAEFEENEDFFEVLGERDVLVYHPYESFDAMTDFIIQASEDEQVMAIKMTLYRVSGKSPLITALANAAESGKQVTVVVELKARFDEERNIAWARKLEQSGCHVVYGLVGLKTHAKVTLIVRQEGPELRRYVHVGTGNYNDSTAKAYTDLSLFTANHEIGLDASELFNQMTGYSANYNWNSFIVAPTNMSLSLQKLILREAEHAAAGRPARIIAKMNSLSNQEVIDNLYSAAQAGVSIDLIVRGVCCLRPGIEGLSERITVRSIVDRFLEHSRIYYFENGGKPEVYLSSADWMTRNLTRRIELMCPVKDSNIRKQIVKILDLSLMDNVKSSFLQPNGYYERADDKKAPFRSQFAAMNVTRWKGGRALPSPTKHS
>NZ_CP009285.1|WP_081972122.1|4613731_4614409_-|LysM-peptidoglycan-binding-domain-containing-protein
MKIKFGAITALAAVLGLGTLLQAAPVQADSVHIAGEATTYYTLSNHYGISMEELMNANPQISASNIYPGLKLAIPGTVQAKTVAVTETAADSVVTNGDLSVLSVEPASNTVQAWGKAFTYAKSIQVKASAYSSAASENGKWGAVDYFGNALKLGTIAVDPSVIPLGTKVLVTGYSHPGLPKQAFLATATDMGSAIKGNRIDIFIPGSQSFVADFGYQYVQLYIIQ
>NZ_CP009285.1|WP_099052548.1|4612817_4613627_+|polysaccharide-deacetylase-family-protein
MILPCIFPSAELASVAAHTSAQPEVSVEEDDAVPAGSTASQSTARRHKKNKGLSLSQLLRKYPDTIKTQGPRRKIIALTFDDVPDPRFTPQLLDVLHKYNVKATFFVVGSRAEKHPGLVARILREGHAIGNHSYNHPEFSKLSMNEFRTQIVRTENIIQVLAGYKPRLIRPPYGDISEQQLKWAKSHGYKLVNWNVDSLDWRGLSKTQVRNNILSRAGKGAIILQHGGGGRGSDLKGTVQALPEVISIMRKRGYSFVTVPQMFEVSKSK
>NZ_CP009285.1|WP_042214399.1|4611534_4612575_-|NADH:flavin-oxidoreductase/NADH-oxidase
MADLFAPYELKALTLKNRVVMPPMCQYAVEKQDGIPTDWHFVHYVSRAVGGTGFIIVEMSGIHPDGRITNQDTGIWDDGQIAAHKRISEAVHTHGARIAIQLGHAGRKAVDANPPVAPSAIPFDAHSKTPHALTRDEIAEMVNAYREAARRAVEAGYDTVELHGAHGYLIHQFHSPLSNVREDEYGKDPILFGEQVTEAVREVLPAEMPLIMRVSAKEYVEGGYNEAYALEFCRRYKAAGVDMFHVSSGGEGPIGSNGGPNAGPGYQVDLAEYIRSGLQVPVIAVGRLESYEEAQAVIAEARAELVAVGRGMLSDPYWVLHAEEALGGIDQASLPKPYVRGFWNKK
>NZ_CP009285.1|WP_042137793.1|4610743_4611448_-|dihydroorotate-dehydrogenase-electron-transfer-subunit
MATVISNERLGDGVYHLVVEGGNGGAMGQFYMLRAWGAYPLLSRPLSIHQVNDSGVDFLYHVVGEGTEILAGLKPGDKLELEGPFGTGFPHVEGKVALVGGGIGIAPLYYCAQELPESDIYLGFSREPFRTEAFRPLAAELTVDVGGHILDSVDFTAYDHIFVCGPHPMLKAAQLKGIAAETAGKRPDVYLSLENRMACGIGACLVCSVSCKDGQRKACADGPVFLAGEVLFHD
>NZ_CP009285.1|WP_042214397.1|4609818_4610751_-|dihydroorotate-dehydrogenase
MINTTATIAGVHFKNPIVMASGTFGFGREYGKLYNVSLLGGISGKGLTLHAKAGNPGVRVYETASGMLNSVGLENPGVEAFLAKELPYWETLDTARIVNLGGNTLADYVLGAELIQRDADARLLRGKPAVDMIELNISCPNVKEGGIAFGVKTPAALEVVRAVRAATRLPLAVKLSPNAEDIAEMAEMCEAEGADAVSLINTISGMKIDVRRRRSVFNNLYAGLSGPAIKPVALRMVHQVSKRVSIPVIGMGGITSATDIIEFIMAGATVIQVGTYNFMNLRAGSTLVEELQQFMAEENISSLDEIRGIV
>NZ_CP009285.1|WP_042214415.1|4621214_4622960_+|alpha-glycosidase
MLLEAMYHVPRDKWAYAYDATTIHLRVRTKRDDVDYVVALTGDKYDWQHTSYDIIMEKAASDDKFDYWEAAVRPKYKRLSYTFRVSKGSETVYLLDNGIRSECPQPPNHFYEFPYIHGIDLFKVPTWAKDAVFYQIMTERFANGNPLNDPEGTEPWGGRPKLDNFFGGDLQGVLDHLDDLQELGINAVYFTPLFVSPSNHKYDIVDYKKVDPHFGDNELLKNVVEECHKRGIRVMLDAVFNHCSDKFPPFQDVLEKGEFSVYRDWFHMNSFPAEIVDGIPTYDTFGFYGNMPKFNTANHEVKSYLLEVAEYWIKEIRVDGWRLDVANEVDHHFWRDFRKVVKAANPDAYIVGEVWSDSLTWLLGDQFDSVMNYPFSGTVLEFFNGGMDGITFGHRIGGLLMRYPQQTNEVVFNLLGSHDTPRLLTVLGEDKRKLKLTVVFLFTFMGTPCIYYGDEIGLTGGEDPDCRKCMEWDQSKQDRELYDFYRMMIALRKEHKALREGRFRILQACENDPCIVYERADERIHFTVWMNNSPQSRTLSHPMETDDWLDALTGEAVVPEAGIMHVALDPYGYRILYRNLD
>NZ_CP009285.1|WP_052429562.1|4623049_4623421_+|nuclear-transport-factor-2-family-protein
MIEREQIIRNYFRSWIDKDNTVLGKIFGPNIIYTECYGPEYHGLDTITKWFDDWNTRGTVLVWTIKQFIHQGSMTAVEWYFKCEYESETEAFDGVSLIEFNPDNLIVNVKEFQSKTPHYYPYT
>NZ_CP009285.1|WP_042214417.1|4623483_4624929_-|glycogen-synthase-GlgA
MKVLFAAAEAHPFIKTGGLADVIGALPKALKAAGVDVRVILPKYKGIAEKYSSQMEHIAVVDVPIGWRNQYCGIQRIIFEGVPVYFIDNEYYFGRDGIYGYMDDGERFAFYNRAVLECLPAINFQPDVLHCHDWHAAVIPLLLQAHYRHNPFYSEMRTVFTIHNLLYQGVFPYSVLGELLGLDNSYFPGVEYYGNVNYMKGGIVYSDHVTTVSPTYADEIRTPYYGYGLDGLLTSRSDALSGIVNGIDTKSYNPASDPSIFTRYRSNLIKKAENKLGLQQELGLPVAPYIPMVAMVTRLVDSKGLDLLTRVLDELLYYDDIQFVMLGTGDEVYERWFREAQWRYPTKLSSQITFSDALSRKIYAASDIFLMPSKFEPCGISQLLALRYGSIPVVRETGGLNDTVHAYNEVTGEGNGFTFKDYNAHDMMHTLRRAVSFYHKPEHWKKVAKNAFTGDYSWNVSAQQYIDIYNKISDKAAVAEQ
>NZ_CP009285.1|WP_042214419.1|4624954_4626874_-|1,4-alpha-glucan-branching-protein-GlgB
MAEIPKTVNLPSSEDIYLFHEGTNYRSYTMLGAHIAVEEGQAGVRFTVWAPHAAYVGLAGDHNSWDGTLDSDSLYKIPDSGFWSRFFPGIEPGTFYKYRITGADGTSFLKADPYAFKAEVRPATASVVANLDGYKWGDAAWRRKSKAPYNAPMNIYEMHFGTWRQKEDGELYTYREMSSLLIPYLTEMSYTHVEFMPLAEHPYDLSWGYQGTGYFAATSRFGEPQDLMYLIDQLHQAGIGVILDWVPAHFAKDAHGLRMFDGSPLYEYEDPMLAEKPGWGTLSFDFSKPEISSFLISNALFWFEKYHIDGMRVDAVTSMLRLDFEKQHHQYRKNKNGGLENLEAIAFIQRLNMTIFQYYPKALMMAEESSAWPGVTSPVHEGGLGFNYKWNMGWMNDTLGYIEHDFGARPYHHNLLTFPIVYAYAENYTLPLSHDEVVHGKKSLLNKMPGSYEQKFAGLRVLLGYQISHPGKKLLFMGGEFGQFIEWKDQDQLDWLLLDYEAHRRMLAYTAALNKLYLTEKALWELDHDMEGYQWIDADDSGQSIASYIRRGKRPVDTLLVIINFQPVERRNYRIGVPRPGTYEEIFSSETREYGGSGIHNEPVKSVKKEWHNQLNSLELTIPPLGFLVLKKSGRKTVN
>NZ_CP009285.1|WP_042214421.1|4627091_4628315_+|glucose-1-phosphate-adenylyltransferase
MSKKDCIAMLLAGGEGRRLAPLTSSMAKPAVPFGGQYRIIDFPLSNCVNSKIDTIGVLTQYEADSLHKHIGEGEPWGLHSRSDKGVKLLPSGIEGRDSYSGTADAIYKNIEYIDSQNPEHVLILSADHIYHMDYRKMLNYHVGKAAKATISVMEVPWDEASRFGVMNVNDDLQISEFAEKPKVPKSNLASMGIYMFEWAYLKAYLLRDAANPESGHDFGKDVIPSMLDANDELFAYRFEGYWRDVGTVDSLWEAHMDLLQSEDGFKLDNSRWPMYSRAYRTKLAAYKPRVQAPPADCLMHESCTMEGSLHRSVIFGGVEIGKLSKIKQSVIMPGVRIGRGVLIENAIIGEGAVIKDGAVIKGSADNIVVVGPHEIVAAKPIIRTQPSRLLQEVYEKTGRLRAEGMPS
>NZ_CP009285.1|WP_052429563.1|4628407_4629493_-|GNAT-family-N-acetyltransferase
MNTQVSGNSFSNQRFEMIRGEREHAADVLKLLREAAGWMESKGINQWTPGQFSIRDVEDYFSSREVYLAMEGAALAGMFTLQFSDVQYWGDRNDESYAYLHRLAVAKSYRGLGLGGQMIRYALRIAEERGCTGLRLDTVAHNIKLNRYYQSMGFRYMGTRDVGAGRLVNLYEYEAETGDSGSVILRYMGEADYTLMREWSVSPEYLKTWAGPSLSYPLDDRQLERYLDVANHPGESSLLVYCAVLRATGQAVGHISLSMIDRENGSARISRVIVDPGSQGRGIGLQMVREVLRIGFDGLRLHRISLGVFDFNTAAQKTYETAGFTREGVSREAALFGGRYADCIEMGILDRDWRANRNPGR
>NZ_CP009285.1|WP_042214424.1|4629489_4630896_-|HAMP-domain-containing-histidine-kinase
MIKKGMRRQIVLHYILVVFVALLLVETIFLLAIRTYYYDSIYSKITTHISAGETFVKYEFSAERSPNQLLNLLDFFNLEYTELEVLTLNGDIITSSTGFQPDRTITTSDVPEAVGGSVGRWVGRQAGTNESVMAVSKMVQINSHETYILRYLTSMEGVNNDLLNLTLLSIGIGAAVMMIVVLFSIGLANSIVRPLNNITAVSAQMAKGKFTTRIKGDYRYEIGELASTLNYMAEEIVRSNQIKDDFISSISHELRTPLTSIKGWSETLISGGYDPEETKLGMGIISKESDRLIGLVEEILDFSKLQQNEMKLSIAQVDIKVLLQETLLNIWAKAEKKRIHLLLECEDTIFIRGDANRLKQVFLNLVDNAVKFSPEDSSIVLSAERLTNTEMAVIVRDSGIGISEAHLSRVRDRFFQVDALNGGTGLGLAISQQIVELHNGKLEMDSELGKGTQVTVILPLDDVQEEKA
>NZ_CP009285.1|WP_039299112.1|4630892_4631591_-|response-regulator-transcription-factor
MSKVLILEDEESIRSFIVINLKRNGFEVLEAADGNEALHKLTTVPDIDIALLDVMVPGIDGFEVCRRIRETNERLGIIFLTAKVQEQDKVYALSVGADDHVSKPFSPTELIARIQSLLRRVNVHREQSAKVSFHSGPFTLDLISKQFKKSGEAIELTPTEFSLVQFFLEKENTPLSRDSLLDHVWGKEYMGDPKIVDVNIRRLRQKIENNPSEPEFLQTVWGHGYKWKGQVQ
>NZ_CP009285.1|WP_174479822.1|4631583_4632870_-|hypothetical-protein
MNKRLLGRLTAASLSLFVISGCTFISDPVSQMRVPQLSADKASLMTAINSSLKPLDATLIRPANDDDSSIFTEDLDKDGIMETLVFYQTKNEAVVIHGMILEKHEDTWVKKLVFDGDGTMLDSVDLRDVTGDGKLDIVTGYSRGEEKGMVVYSYSGGELEEILTKPYTKYILDDLNEDGIADITVVYFKRNEFATITTYQYNDSFKVLDELDDLDPYFDNYYNIVSGKVAENKEGIVLDSAVDSRSAYTTIVVMENNKLRVAIPGDVRTFKDRKIVSEDIDLDGIIEIGMLEPPSGWEYFDPETIPYFNSYYKWDGKDGLTFSTQLYNDPSDRFTINFSPEWHENVTVDTKSVQDKSLKFITLDTGETVAEVSFFSPAEWDRVKNSGWKLLGRDLDKMIGYRGELEQNTIGGEDGRVKSSIERKGIDE
>NZ_CP009285.1|WP_039299118.1|4632906_4633632_-|ATP-binding-cassette-domain-containing-protein
MITVEHLAKAVGEDKAPVLQDIGFQLEPGEFVVILGASGSGKSTLLKCLALREKWDRGNFRVDGRDIMKSPFAGKRKIRREWAYLEQNAELNPNRTALKNVLIGQASQTPLWRMATGMVRSDDYMGAMDQLDLLGLLDKAKMKTSHLSGGERQRVAIARALVHGAKVILADEPVTGLDPKTAENVLETLRKLCKETGLTVITVLPIELAERFASRLWVLEDGRIKHDVKGRRLTSQERLHL

Crispr_ID: NZ_CP009285_12

• CRISPR_ID: NZ_CP009285_12
• CRISPR_location: 4740138-4740211
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: csa3

Consensus repeat of NZ_CP009285_12

Consensus_repeat	Method
ATAAAGGATTCTCAGTCCGCTTCA	CRISPRCasFinder

spacers of NZ_CP009285_12

>12.1|4740162|26|NZ_CP009285|CRISPRCasFinder
CCCCGGTTACGGGGCTTTTTGACGAA

CRISPR arrays and Neighbor proteins around NZ_CP009285_12

CRISPR arrays

The CRISPR arrays of NZ_CP009285_12

>merge|NZ_CP009285|12|4740138-4740211|CRISPRCasFinder
ATAAAGGATTCTCAGTCCGCTTCACCCCGGTTACGGGGCTTTTTGACGAAATAACGGATTCTCAGTCCGCTTCA

>NZ_CP009285|12|11|4740138-4740211|CRISPRCasFinder
ATAAAGGATTCTCAGTCCGCTTCA	CCCCGGTTACGGGGCTTTTTGACGAA
ATAACGGATTCTCAGTCCGCTTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042214625.1|4748975_4749854_-|nitrogenase-iron-protein	unknown	unknown	gnl|CDD|273538
NZ_CP009285.1|WP_042214611.1|4735080_4735596_+|MogA/MoaB-family-molybdenum-cofactor-biosynthesis-protein	unknown	unknown	gnl|CDD|238451
NZ_CP009285.1|WP_042214606.1|4733448_4733796_-|four-helix-bundle-copper-binding-protein	unknown	unknown	gnl|CDD|153434
NZ_CP009285.1|WP_052429569.1|4736152_4737181_+|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl|CDD|238042
NZ_CP009285.1|WP_042214626.1|4750596_4751118_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_052429571.1|4744122_4745121_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223673
NZ_CP009285.1|WP_052429573.1|4749887_4750244_-|hypothetical-protein	unknown	unknown	gnl|CDD|238315
NZ_CP009285.1|WP_042214608.1|4733887_4734898_-|GTP-binding-protein	unknown	unknown	gnl|CDD|223597
NZ_CP009285.1|WP_042214600.1|4731565_4732276_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042214622.1|4745136_4746231_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|223787
NZ_CP009285.1|WP_052429570.1|4739048_4739867_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|223912
NZ_CP009285.1|WP_042214620.1|4741754_4743236_-|nitrogenase	unknown	unknown	gnl|CDD|238932
NZ_CP009285.1|WP_081972128.1|4743232_4744126_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224041
NZ_CP009285.1|WP_052429568.1|4732272_4733238_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP009285.1|WP_052429572.1|4747615_4748950_-|nitrogenase-cofactor-biosynthesis-protein-NifB	unknown	unknown	gnl|CDD|273539
NZ_CP009285.1|WP_042214617.1|4740448_4741771_-|hydrogenase	unknown	unknown	gnl|CDD|238931
NZ_CP009285.1|WP_081972125.1|4735711_4735927_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042214597.1|4731069_4731534_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042214615.1|4737212_4738010_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|223912
NZ_CP009285.1|WP_042214623.1|4746261_4747581_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase	unknown	unknown	gnl|CDD|225428

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009285.1|WP_052429569.1|4736152_4737181_+|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	6.3e-13	43.9	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042214625.1|4748975_4749854_-|nitrogenase-iron-protein	gnl|CDD|273538	TIGR01287, Nitrogenase_iron_protein_2, nitrogenase iron protein. This model describes nitrogenase (EC 1.18.6.1) iron protein, also called nitrogenase reductase or nitrogenase component II. This model includes molybdenum-iron nitrogenase reductase (nifH), vanadium-iron nitrogenase reductase (vnfH), and iron-iron nitrogenase reductase (anfH). The model excludes the homologous protein from the light-independent protochlorophyllide reductase. [Central intermediary metabolism, Nitrogen fixation].	3.00261e-156
NZ_CP009285.1|WP_042214611.1|4735080_4735596_+|MogA/MoaB-family-molybdenum-cofactor-biosynthesis-protein	gnl|CDD|238451	cd00886, MogA_MoaB, MogA_MoaB family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF) an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea, and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MogA, together with MoeA, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes. In contrast, MoaB shows high similarity to MogA, but little is known about its physiological role. All well studied members of this family form highly stable trimers.	3.53455e-62
NZ_CP009285.1|WP_042214606.1|4733448_4733796_-|four-helix-bundle-copper-binding-protein	gnl|CDD|153434	cd08026, DUF326, Cysteine-rich 4 helical bundle widely conserved in bacteria. This functionally uncharacterized protein forms a 4-helical bundle with a bromodomain-like topology. It is present in major bacterial lineages and contains highly conserved cysteines in a repeated pattern, whose sidechains appear buried. Some family members have been (mis)annotated as putative ferredoxins.	5.41201e-26
NZ_CP009285.1|WP_052429571.1|4744122_4745121_-|ABC-transporter-permease-subunit	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	1.06904e-40
NZ_CP009285.1|WP_052429573.1|4749887_4750244_-|hypothetical-protein	gnl|CDD|238315	cd00562, NifX_NifB, This CD represents a family of iron-molybdenum cluster-binding proteins that includes NifB, NifX, and NifY, all of which are involved in the synthesis of an iron-molybdenum cofactor (FeMo-co) that binds the active site of the dinitrogenase enzyme. This domain is a predicted small-molecule-binding domain (SMBD) with an alpha/beta fold that is present either as a stand-alone domain (e.g. NifX and NifY) or fused to another conserved domain (e.g. NifB) however, its function is still undetermined.The SCOP database suggests that this domain is most similar to structures within the ribonuclease H superfamily. This conserved domain is represented in two of the three major divisions of life (bacteria and archaea).	2.73004e-22
NZ_CP009285.1|WP_042214608.1|4733887_4734898_-|GTP-binding-protein	gnl|CDD|223597	COG0523, COG0523, Putative GTPases (G3E family) [General function prediction only].	2.8631e-77
NZ_CP009285.1|WP_052429568.1|4732272_4733238_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.04782e-56
NZ_CP009285.1|WP_042214622.1|4745136_4746231_-|ABC-transporter-substrate-binding-protein	gnl|CDD|223787	COG0715, TauA, ABC-type nitrate/sulfonate/bicarbonate transport systems, periplasmic components [Inorganic ion transport and metabolism].	1.36299e-35
NZ_CP009285.1|WP_052429570.1|4739048_4739867_+|ABC-transporter-permease	gnl|CDD|223912	COG0842, COG0842, ABC-type multidrug transport system, permease component [Defense mechanisms].	2.63266e-08
NZ_CP009285.1|WP_042214620.1|4741754_4743236_-|nitrogenase	gnl|CDD|238932	cd01972, Nitrogenase_VnfE_like, Nitrogenase_VnfE_like: VnfE subunit of the VnfEN complex_like. This group in addition to VnfE contains a subset of the alpha subunit of the nitrogenase MoFe protein and NifE-like proteins. The nitrogenase enzyme system catalyzes the ATP-dependent reduction of dinitrogen to ammonia. NifEN participates in the synthesis of the iron-molybdenum cofactor (FeMoco) of MoFe protein of the molybdenum(Mo)-nitrogenase. NifB-co (an iron and sulfur containing precursor of the FeMoco) from NifB is transferred to NifEN where it is further processed to FeMoco. VnfEN may similarly be a scaffolding protein for the iron-vanadium cofactor (FeVco) of the vanadium-dependent (V)-nitrogenase. NifE and NifN are essential for the Mo-nitrogenase, VnfE and VnfN are not essential for the V-nitrogenase. NifE and NifN can substitute when the vnfEN genes are inactivated.	0
NZ_CP009285.1|WP_081972128.1|4743232_4744126_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224041	COG1116, TauB, ABC-type nitrate/sulfonate/bicarbonate transport system, ATPase component [Inorganic ion transport and metabolism].	1.296e-120
NZ_CP009285.1|WP_052429572.1|4747615_4748950_-|nitrogenase-cofactor-biosynthesis-protein-NifB	gnl|CDD|273539	TIGR01290, FeMo_cofactor_biosynthesis_protein_NifB, nitrogenase cofactor biosynthesis protein NifB. This model describes NifB, a protein required for the biosynthesis of the iron-molybdenum (or iron-vanadium) cofactor used by the nitrogen-fixing enzyme nitrogenase. NifB belongs to the radical SAM family, and the FeMo cluster biosynthesis process requires S-adenosylmethionine. Archaeal homologs lack the most C-terminal region and score between the trusted and noise cutoffs of this model. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other, Central intermediary metabolism, Nitrogen fixation].	8.99503e-179
NZ_CP009285.1|WP_042214617.1|4740448_4741771_-|hydrogenase	gnl|CDD|238931	cd01971, Nitrogenase_VnfN_like, Nitrogenase_vnfN_like: VnfN subunit of the VnfEN complex-like. This group in addition to VnfN contains a subset of the beta subunit of the nitrogenase MoFe protein and NifN-like proteins. The nitrogenase enzyme system catalyzes the ATP-dependent reduction of dinitrogen to ammonia. NifEN participates in the synthesis of the iron-molybdenum cofactor (FeMoco) of MoFe protein of the molybdenum(Mo)-nitrogenase. NifB-co (an iron and sulfur containing precursor of the FeMoco) from NifB is transferred to NifEN where it is further processed to FeMoco. VnfEN may similarly be a scaffolding protien for the iron-vanadium cofactor (FeVco) of the vanadium-dependent (V)-nitrogenase. NifE and NifN are essential for the Mo-nitrogenase, VnfE and VnfN are not essential for the V-nitrogenase. NifE and NifN can substitute when the vnfEN genes are inactivated.	0
NZ_CP009285.1|WP_052429569.1|4736152_4737181_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	6.68031e-14
NZ_CP009285.1|WP_042214615.1|4737212_4738010_+|ABC-transporter-permease	gnl|CDD|223912	COG0842, COG0842, ABC-type multidrug transport system, permease component [Defense mechanisms].	7.25714e-10
NZ_CP009285.1|WP_042214623.1|4746261_4747581_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase	gnl|CDD|225428	COG2873, MET17, O-acetylhomoserine sulfhydrylase [Amino acid transport and metabolism].	0

Protein sequences

>NZ_CP009285.1|WP_052429570.1|4739048_4739867_+|ABC-transporter-permease
MRPGGLWMTIAAELTKQHRNRRKGRATFFSLLFWPIISFLTSYYTMKPYRTGEGSVLSRIIPDERIPLFLLSGYLVFQLFWTVVETAWIFEQERRDGTVETVFLTPASKIAFLYGRSLYSLLHGIWMFAAFSILTFVFVSDTASVNWAALTLALLLITIAAIIWGAMLSAVSLFSRESSFLYYIFQTPMELFGGVRIPPAVFPAWATGLSALFPVTYSLILVRGALYGTTGRVWWLALTVLMAGSLLLAGCTRYILYRAERHARLKGNWSLF
>NZ_CP009285.1|WP_042214615.1|4737212_4738010_+|ABC-transporter-permease
MWQTAIATAVRNQRSNLRAFPWNFTLGHIIEGAYLVLVAYFSYVYLIQGDLDDKFALYTGTHNYLAFAIIGGTLNIFCVSMMMNVSRSLITEWREGTLEALLLSPSSRNGYFLGTAVQQFYRSGLILAAVLAFGILAGLRLPVPHLLSVLAGAFLFILSTYAMALVMGSVMLLTRDTYIVQNTLFTVMTLLCGFQFPRQYLPRFLQIAAEIFPLTTSLQLLRGALLTGETVSLTDLLPALLLSLVYIAVGLWCISRVERRLFEKF
>NZ_CP009285.1|WP_052429569.1|4736152_4737181_+|winged-helix-turn-helix-transcriptional-regulator
MQRKIRTVVCPYHEMLCSLHVLHQPEHHPKRLHWAKELLSRMSPSLAEGIQTIGRLSDSWTGLTLMDRLGSFSSSQEGIRVLKALPDTELIHVMLNGRISLGTILEWQHGLLPGHGKPVTPPDEPARYLLKHLESVRNLLITTLEDYEQEYFRKEWEYIQPWIHTAAAQFQEAAARSAEKALNSLHPRLHAAEGTITAQKAVTYHFEYEQLQQIFVLSSTFIFPHLLIDWTGDKGRLMLPLAVDIPGLAFNEAPPEDLLRQFRGLGDATRLRMLKLLWQAPHCTKQLAPVLGISEAAVSKQLKLLSEAGLVTSERKGNYLFYSSSKEAFDSLIVLQRQYFEQ
>NZ_CP009285.1|WP_081972125.1|4735711_4735927_+|hypothetical-protein
MRNCPKCPVQTVTDPTEVVYEDYYHPQVVQVIHHVEVVRRHHCVPVPQHIYTYSVRDEMCGISAATRGRRR
>NZ_CP009285.1|WP_042214611.1|4735080_4735596_+|MogA/MoaB-family-molybdenum-cofactor-biosynthesis-protein
MTSVEEHRREAPDSVACYIITVSDTRTMETDTGGPLIQNMLEEAGYTVIGRTIVKDDYEDIRELVYKNSVHSGIEAVLLTGGTGISPRDTTYEAVASLLDKSLPGFGEIFRLLSFTEDIGSAAMLSRAIAGTIGSTAVFSMPGSTGAIKLAMERLILPELRHVMREIYKRS
>NZ_CP009285.1|WP_042214608.1|4733887_4734898_-|GTP-binding-protein
MEQSLPVYILSGFLGSGKTTLLQRLLEHWKTQGLRPAVIMNELGEVNLDGLLVEQSVPMAEMLGGCICCTSRGDLSTELTTLVKKESPDVVVIEATGAANPLEIVDAVTETSLYQQVELKGLITVVDAAHLLELYRSQQGATYRLMQEQIRCASVLILNKTDRINAEEAEEITAVLRKWNAYAGILPAVRCELEPEALLGNIGGVYTEDRDSAEEHVHNAQDGQAGQVHASHDHVMAYTHYFKNPVNSEEFERFVKELPRDVYRAKGIVSFNDTSSRFLFQYAYREADFMKITPQGEVPDVAVFIGEHFSSSGLRTELLRLEKRLPARPAAVKRSL
>NZ_CP009285.1|WP_042214606.1|4733448_4733796_-|four-helix-bundle-copper-binding-protein
MTRIQYQECIDACIKCMDACNYSYVSSLKEYDLAALRESIQLDRECADMCSFAIQAMTRQSPFVVEILRLCADICERCADASSRHEHNHCQSCIDACRSAAMACRLVSGAVEVYA
>NZ_CP009285.1|WP_052429568.1|4732272_4733238_-|ABC-transporter-ATP-binding-protein
MILQSTDRIILPEDTEVPPLITLTRGSKLYGSRPVLNEISMIIRPGTATALIGRNGSGKSTLLSILAGLLRLSSGELTYGRHGLTTGYAPEAFPGLKLTAEDYLHHMGRLAGLSRAVTESRVSGLLDTFKLEAFRSRPMAGFSKGMLQKVNLIQSLLIRPQLLLLDEPMSGLDIPAQHILMELLQELKSEGTALVFSVHEVQTVEALADTVYVLQEGQVIRMIHGAENLRPAPAVHIIYTDLPPVEQESVKAWPGVLSMLPAPETAGTACTSLTVEQSVSDACLKQILAAGGSIVSVERLGESSGIAAWMDPKDQKGSGRG
>NZ_CP009285.1|WP_042214600.1|4731565_4732276_-|hypothetical-protein
MKALIGYFLHSYSVSQRYFGPVAGIIIAVLILYSYKPNPVMNSYSATAVFLFVACAWLGLSFLNHEHAVQKQVAIVQLRSARRYSIGGILTLVLLTLLLDLFIVIYPVVTGSFNEPAGLGRILLAFTGHALLGVLGIAISLYLQSSWVSRTSYAAGLMLITIILSVSAGKVAELVPGPIVPVLLPPVYPVMDAMMNADALPLSSLLGAYAHVLVYIILLTGFYIYRSGRMDYNKTI
>NZ_CP009285.1|WP_042214597.1|4731069_4731534_-|hypothetical-protein
MKDTQVPESEQSKELFAYFGLAVYYCQALEQQLTNLLLLTKLSQGKTPTDAEIAELYQRKLSNSLGQLIKEIQHHFPFSEEETSQLQAVWKERNHIVHDYFKERIQETFTPAGRAHMIRELKRFKNKASRLEIKLQGYCTEMYSKLGLEEEHIK
>NZ_CP009285.1|WP_042214617.1|4740448_4741771_-|hydrogenase
MSKLIEQPRYSCALGVQQSVIAIHRAVPVVHAGPGCSTKIHGFLGQGEGYAGGSTIPCTNSSEAEIVFGGENKLRGVIHGAFKVIDADLFVVLTGCTSDIVGDDVGQVTREFQAAGKPVVYAETGGFKSNNYVSHDLIIKAIVEQYVDKFAADKTSVIPGLVNVFASVPYQDPYWIGNLQELKRILTGIGLTVSVLFGPESGGVEEWLSIPRAEFNIVVSAWPGLKSAQLLEAKYGTPFYHFPYLPVGGIETGRFLREVADFSSVDRAAAKAFIAEEERKFYTHIERTADFMLEFRYGLPRVFYTMLDASYAVGLAKYLLNELGILPAQTQYVVDNTPEEYRAAIVERFRTISSRRSANVEFVEDGGAIQEAIRLDKPAQRALILGSGWERDLAAELGADLLPVSVPITYRLILNCGYAGYNGGLRLIEDIYDRVLGTYR
>NZ_CP009285.1|WP_042214620.1|4741754_4743236_-|nitrogenase
MSKVNLNTPEVPVRELRLGSITGFSGTAAGLVSCSNAGGLKDGSRSFSQCMGCSSGNAFCQLSMITDAAMVNHAPVGCAGDFFGYNFVYRVGQMERDLPPVIGRYFNTNIEEMDTVFGGARKLEATIRLAFERAKPKAIFVTTSCASGIIGDDVESVTNKMTRELGIPVVTCFCEGFKSKIWTSGFDSAYHSIVRKIVKPPEKKTNKVNIINFWGSDVFSGLLNKLGYEADYIVPFSTVAQLERISEAAATIQICPTLGTYLGAALEQVYGVPEIKAPVAYGLAGTDAWMRELGRVLDREQEIEEIIAVEKAAVLPKLEEYRARLTGTTCYITAGSAHGHALIALLRELGIDVQGAAIFHHDPVYDNGDPAADMLDHTVKTYGDVPNYNVCNKQAYELANILNRVRPDLMIARHGGMTHWGAKLGIPTLLIGDEHFSWGYQGLLNYAERILETLDNKEFVTNLAKHSTMPYTKWWMEQPPYTFLGGNVHVQAY
>NZ_CP009285.1|WP_081972128.1|4743232_4744126_-|ABC-transporter-ATP-binding-protein
MSRRETAGGIAREADQAGEPGTFGTVRGAVSIRKVSRSYEEDTGRRVEALKEVELEIESGSFVSFIGPSGCGKTTLMRLIAGLDECASGEITLDGERIHGPHYERGYVFQQANLFPWMTIRQNISAGLKARKVYQENRRKPDEFIRMVGLEGFGNAYPHQVSGGMAQRASLARALINQPKVLMLDEPLGALDAFTRMNLQDELLRLWRLHGTTMILVTHDVDEAVYLSDRIVIMSARPGQIKEIIEVEMEHPRDRGSSEFVFLRSRILETLHFAGSSASLEYYPVGHPAATRKGRRT
>NZ_CP009285.1|WP_052429571.1|4744122_4745121_-|ABC-transporter-permease-subunit
MSLVNRNLVLGGRTREAFRIPDPLRAGLPLVSFGTALMLSLVLQSRQDVEQLPYRITLLAFIVYFALHFLLRGRISGRRWQQVLYKSPFYLVLGFVLAGWDVLTTKLEVLPLPFVPGLAQILSVMVNDAQMLLISTAYSLRLLVIGFVIGSLIGIVLGVLIGWYRKWNYWLFPVLKVMGVVPATALIPIVMILVPSSFYAAVLLIVIAVCFPVAFMTSVGIANVQNTYFEAARTLGADERFLIFRVAIPGAMPSIFSGIYTATGISFATLVVSEMIGARAGLGWYINWAKGWSDYAKVYASIIIMAVTFSIVMAIIFRVRDKVLKWQKGLVK
>NZ_CP009285.1|WP_042214622.1|4745136_4746231_-|ABC-transporter-substrate-binding-protein
MNTSKKLPAVLLVTSALLVVTACGNNAANQKTSANNHNHSTSAPAVAAVAPSSNAAASNSSKAAPASYKYGKLKIQALSGAVCGAPSYVAYEKGFFAEEGLDVELVSGSMDAMKTGLTTGEFTVTNGDFVWFTSIQQGLDLKVIGGLHHGCIKLVVPPGSDIKTAADLKGKRIGVDEIGGVPMAVASVVVTNAGLDPQKDVQWLAYPLDQLQEGVKKGEIDVYAAWDPFGKLAEVNNGYTVLADISTDSNFAGKSCCFLYASGKQIEEDPERVAAIARAYQKATAWIAEHPEETAKLEIEKKYVATDDVKLVTDLIESYHFNYTTDAAQEDIRYFVKQFSKTGFLKKDTDPDEFLKKAYYDVFK
>NZ_CP009285.1|WP_042214623.1|4746261_4747581_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase
MADHNLGFDTLKVRAGYDSREHNYAVAVPIYQTASYDLGSVGRAEKLFGMEEAGYLYTRIANPTVAVLEQRLTALDKGTGAVAVASGMAAVTYALLNLAEGGGRIVTTPRLYGGSFDALKHLYPKFGVHVDFVEDSDDPEAFRRAVRPDTKAILIESISNPNSTILDIEAIAAVAHENGLPLVIDNTFGTPYLFDSFAHGADIIVYSATKAIGGHGTTLGGVIVENGKFDWAGGRFPHFAEPQYLLREQETGRERSILEVFPEAPFTARVRLSYLAYFGAALSPFDAFLLLQGTETLSERISKQVANALRIVDYLQKNDRVSWVSHPAADGNPYQALAARYFPKGAGSIFTFGFGGNEEQLRTFLNAVKLFSYHANVGDARSLIINSPKTTHGELNAEDQAAAGITPDTIRLSIGLEDADDLIRDLEQAFAAAFVESLV
>NZ_CP009285.1|WP_052429572.1|4747615_4748950_-|nitrogenase-cofactor-biosynthesis-protein-NifB
MHVTEYWGGSGLQNVQRHPCYDELAHEVFARMHLAVAPKCNINCNYCNIKYDCVSESRPGVVSQVLTPEEARRSVQQTLKVLPQLTVVGIAGPGDPLANPVQTFETFRLLSREMPDLQLCLSTNGLKLPDYVEEITGCGINHVTVTMNALDPAIGGRIYHSIYYRGKAYRGEAAAAILISRQLEGISAMAARGIKVKVNSVLIPGVNDDHLIEVTRAAREAGAFSHNIMPLIISPGSRFERDGRLAPDPGLTLKVQERSAELMPIMRHCRQCRADAVGLLGEDRGGELLAGLPEYSPEERELRLMQLDGELEVRRNRQASGRSPGASATRIAVATRGGGRVNLHFGHASEFLVYEVEEDSYRLLGVRKIQAYCNGTASCGEADAAAILKESAELLRDCQLLLCSGIGSFPQEVLRQADIMAVVTKDDIGVSLLKYGRLLSYFKI
>NZ_CP009285.1|WP_042214625.1|4748975_4749854_-|nitrogenase-iron-protein
MVKKLKQIAIYGKGGIGKSTTTSNISAALSVAGYKVMQFGCDPKSDSTNTLRGGEYIPTVLDSLRDNHAVKAQDVIFQGFNGIYCVEAGGPAPGVGCAGRGIITSVSLMKQQRVFEELDLDFVIYDVLGDVVCGGFAVPVREGIAEHVYTVTSADFMAIYAANNLFKGIHKYSQDGGALLGGVIANSINAPYAKEIVDDFVSRTDTRVVEYVPRSLTVTQSELQGKTTIEAAPDSEQARVYRSLAQNIAEHTVSKVPAPLETNELRQWAADWGKRLVQQDSGLAAPAAAGSL
>NZ_CP009285.1|WP_052429573.1|4749887_4750244_-|hypothetical-protein
MTWKIAIGSVDGININQHFGRCDRFLIYRMEPEGSYSIIEDRSYDRQAEAAGHDTHSLQNTAALLADCSIVLVSHIGPGARALLYEQGIQAMAVEAPIEQAMERLVHFLRSGRGAILQ
>NZ_CP009285.1|WP_042214626.1|4750596_4751118_-|hypothetical-protein
MKRRLAGVLAAALTAGTLLAGCSGEQDQKEAGSYTMQAYQDGTMLAYSQGKGLDGRFRKEMRQAFATEQLALTDEKFTEDNRGNTSYQYLINSQPAQNITLHVFTSRPERVSRITDWYGGMPLAETSGARTEVFNKDNTSLVYTSMGKEKGKYSKKVKDLFAGLLEHLGTHAH

Crispr_ID: NZ_CP009285_13

• CRISPR_ID: NZ_CP009285_13
• CRISPR_location: 4932781-4932867
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_13

Consensus_repeat	Method
AAGTTTTGTGAGCGTTAGCATCC	CRISPRCasFinder

spacers of NZ_CP009285_13

>13.1|4932804|41|NZ_CP009285|CRISPRCasFinder
TGAAACAGCTTCAAACAAAACTGTTCCGGAAGCATAGGCTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_13

CRISPR arrays

The CRISPR arrays of NZ_CP009285_13

>merge|NZ_CP009285|13|4932781-4932867|CRISPRCasFinder
AAGTTTTGTGAGCGTTAGCATCCTGAAACAGCTTCAAACAAAACTGTTCCGGAAGCATAGGCTTAAGTTTTGTGAGCATTAGCATCC

>NZ_CP009285|13|12|4932781-4932867|CRISPRCasFinder
AAGTTTTGTGAGCGTTAGCATCC	TGAAACAGCTTCAAACAAAACTGTTCCGGAAGCATAGGCTT
AAGTTTTGTGAGCATTAGCATCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042214893.1|4924422_4925736_-|flagellar-protein-export-ATPase-FliI	unknown	unknown	gnl|CDD|181092
NZ_CP009285.1|WP_042214902.1|4929214_4929523_-|flagellar-hook-basal-body-complex-protein-FliE	unknown	unknown	gnl|CDD|376721
NZ_CP009285.1|WP_042214918.1|4938777_4939935_-|ADP-forming-succinate--CoA-ligase-subunit-beta	unknown	unknown	gnl|CDD|234813
NZ_CP009285.1|WP_042214925.1|4941505_4943233_-|YifB-family-Mg-chelatase-like-AAA-ATPase	unknown	unknown	gnl|CDD|129465
NZ_CP009285.1|WP_174479825.1|4936510_4937629_-|DNA-protecting-protein-DprA	unknown	unknown	gnl|CDD|223829
NZ_CP009285.1|WP_042214899.1|4927590_4929180_-|flagellar-M-ring-protein-FliF	unknown	unknown	gnl|CDD|235668
NZ_CP009285.1|WP_042214906.1|4930004_4930412_-|flagellar-basal-body-rod-protein-FlgB	unknown	unknown	gnl|CDD|180196
NZ_CP009285.1|WP_042214922.1|4940909_4941338_+|organic-hydroperoxide-resistance-protein	unknown	unknown	gnl|CDD|274649
NZ_CP009285.1|WP_042214927.1|4943445_4943955_-|metallophosphoesterase	unknown	unknown	gnl|CDD|277336
NZ_CP009285.1|WP_039295147.1|4932221_4932764_-|ATP-dependent-protease-subunit-HslV	unknown	unknown	gnl|CDD|235477
NZ_CP009285.1|WP_042214920.1|4940293_4940761_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP009285.1|WP_042214909.1|4930787_4932188_-|ATP-dependent-protease-ATPase-subunit-HslU	unknown	unknown	gnl|CDD|235364
NZ_CP009285.1|WP_042214912.1|4932912_4934292_-|FADH(2)-oxidizing-methylenetetrahydrofolate--tRNA-(uracil(54)-C(5))--methyltransferase-TrmFO	unknown	unknown	gnl|CDD|235416
NZ_CP009285.1|WP_042214904.1|4929551_4929998_-|flagellar-basal-body-rod-protein-FlgC	unknown	unknown	gnl|CDD|235556
NZ_CP009285.1|WP_042214914.1|4934315_4936412_-|type-I-DNA-topoisomerase	unknown	unknown	gnl|CDD|235516
NZ_CP009285.1|WP_042138160.1|4926569_4927586_-|flagellar-motor-switch-protein-FliG	unknown	unknown	gnl|CDD|235561
NZ_CP009285.1|WP_052429577.1|4943989_4944403_-|hypothetical-protein	unknown	unknown	gnl|CDD|223244
NZ_CP009285.1|WP_039295139.1|4937812_4938742_-|succinate--CoA-ligase-subunit-alpha	unknown	unknown	gnl|CDD|180194
NZ_CP009285.1|WP_042214896.1|4925728_4926577_-|flagellar-biosynthesis-protein	unknown	unknown	gnl|CDD|235850
NZ_CP009285.1|WP_042214890.1|4923972_4924416_-|flagellar-export-protein-FliJ	unknown	unknown	gnl|CDD|225437

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042214893.1|4924422_4925736_-|flagellar-protein-export-ATPase-FliI	gnl|CDD|181092	PRK07721, fliI, flagellar protein export ATPase FliI.	0
NZ_CP009285.1|WP_042214902.1|4929214_4929523_-|flagellar-hook-basal-body-complex-protein-FliE	gnl|CDD|376721	pfam02049, FliE, Flagellar hook-basal body complex protein FliE.	1.77033e-23
NZ_CP009285.1|WP_042214918.1|4938777_4939935_-|ADP-forming-succinate--CoA-ligase-subunit-beta	gnl|CDD|234813	PRK00696, sucC, ADP-forming succinate--CoA ligase subunit beta.	0
NZ_CP009285.1|WP_042214925.1|4941505_4943233_-|YifB-family-Mg-chelatase-like-AAA-ATPase	gnl|CDD|129465	TIGR00368, Uncharacterized_protein_YifB, Mg chelatase-related protein. The N-terminal end matches very strongly a pfam Mg_chelatase domain. [Unknown function, General].	1.36905e-175
NZ_CP009285.1|WP_174479825.1|4936510_4937629_-|DNA-protecting-protein-DprA	gnl|CDD|223829	COG0758, Smf, Predicted Rossmann fold nucleotide-binding protein involved in DNA uptake [DNA replication, recombination, and repair / Intracellular trafficking and secretion].	9.11819e-103
NZ_CP009285.1|WP_042214899.1|4927590_4929180_-|flagellar-M-ring-protein-FliF	gnl|CDD|235668	PRK06007, fliF, flagellar basal body M-ring protein FliF.	9.35236e-128
NZ_CP009285.1|WP_042214906.1|4930004_4930412_-|flagellar-basal-body-rod-protein-FlgB	gnl|CDD|180196	PRK05680, flgB, flagellar basal body rod protein FlgB; Reviewed.	1.43488e-36
NZ_CP009285.1|WP_042214922.1|4940909_4941338_+|organic-hydroperoxide-resistance-protein	gnl|CDD|274649	TIGR03561, organ_hyd_perox, peroxiredoxin, Ohr subfamily. pfam02566, OsmC-like protein, contains several deeply split clades of homologous proteins. The clade modeled here includes the protein Ohr, or organic hydroperoxide resistance protein. [Cellular processes, Detoxification].	1.80226e-66
NZ_CP009285.1|WP_042214927.1|4943445_4943955_-|metallophosphoesterase	gnl|CDD|277336	cd07390, MPP_AQ1575, Aquifex aeolicus AQ1575 and related proteins, metallophosphatase domain. This family includes bacterial and archeal proteins homologous to AQ1575, an uncharacterized Aquifex aeolicus protein. AQ1575 may play an accessory role in DNA repair, based on the close proximity of its gene to Holliday junction resolvasome genes. The domain present in members of this family belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	4.3366e-36
NZ_CP009285.1|WP_039295147.1|4932221_4932764_-|ATP-dependent-protease-subunit-HslV	gnl|CDD|235477	PRK05456, PRK05456, ATP-dependent protease subunit HslV.	1.3605e-118
NZ_CP009285.1|WP_042214920.1|4940293_4940761_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	4.76304e-20
NZ_CP009285.1|WP_042214909.1|4930787_4932188_-|ATP-dependent-protease-ATPase-subunit-HslU	gnl|CDD|235364	PRK05201, hslU, ATP-dependent protease ATPase subunit HslU.	0
NZ_CP009285.1|WP_042214912.1|4932912_4934292_-|FADH(2)-oxidizing-methylenetetrahydrofolate--tRNA-(uracil(54)-C(5))--methyltransferase-TrmFO	gnl|CDD|235416	PRK05335, PRK05335, tRNA (uracil-5-)-methyltransferase Gid; Reviewed.	0
NZ_CP009285.1|WP_042214904.1|4929551_4929998_-|flagellar-basal-body-rod-protein-FlgC	gnl|CDD|235556	PRK05681, flgC, flagellar basal body rod protein FlgC; Reviewed.	8.35083e-66
NZ_CP009285.1|WP_042214914.1|4934315_4936412_-|type-I-DNA-topoisomerase	gnl|CDD|235516	PRK05582, PRK05582, type I DNA topoisomerase.	0
NZ_CP009285.1|WP_042138160.1|4926569_4927586_-|flagellar-motor-switch-protein-FliG	gnl|CDD|235561	PRK05686, fliG, flagellar motor switch protein G; Validated.	5.33771e-164
NZ_CP009285.1|WP_052429577.1|4943989_4944403_-|hypothetical-protein	gnl|CDD|223244	COG0166, Pgi, Glucose-6-phosphate isomerase [Carbohydrate transport and metabolism].	0.00141636
NZ_CP009285.1|WP_039295139.1|4937812_4938742_-|succinate--CoA-ligase-subunit-alpha	gnl|CDD|180194	PRK05678, PRK05678, succinyl-CoA synthetase subunit alpha; Validated.	0
NZ_CP009285.1|WP_042214896.1|4925728_4926577_-|flagellar-biosynthesis-protein	gnl|CDD|235850	PRK06669, fliH, flagellar assembly protein H; Validated.	4.58673e-31
NZ_CP009285.1|WP_042214890.1|4923972_4924416_-|flagellar-export-protein-FliJ	gnl|CDD|225437	COG2882, FliJ, Flagellar biosynthesis chaperone [Cell motility and secretion / Intracellular trafficking and secretion / Posttranslational modification, protein turnover, chaperones].	1.38371e-15

Protein sequences

>NZ_CP009285.1|WP_039295147.1|4932221_4932764_-|ATP-dependent-protease-subunit-HslV
MLPSFHATTICAVRHDGHAAIAGDGQVTFGESVIMKTTAKKVRRLYRGQVIAGFAGSVADAITLFEKFEGKLEEHHGNLQRAAVELAKDWRQDRILRKLEALMIVMDKEGMLLISGNGEIIEPDDDVLAIGSGGNFALASGRALKRHASHLGAADIAREALQIASEICVYTNSNIIVEQL
>NZ_CP009285.1|WP_042214909.1|4930787_4932188_-|ATP-dependent-protease-ATPase-subunit-HslU
MVNQSLTPRQIVAELDKYIVGQKQAKKSVAVALRNRYRRSLLSEELRDEVVPKNILMIGPTGVGKTEIARRLAKLVNAPFIKVEATKFTEVGYVGRDVESMVRDLVETSIRMVKLERTEKVKDRAEELANDRIVAILVPSTSKGKSQRNPFEMIFGGNNGGAEETKEEAEDGSLSERRRGIKFKLLAGQLEDDIIEIDVEDTTPSMMDMFAGQGNDQMGMNMQEMFGSLLPKRTKKRKLPIREARKVLIQDEAAKLIDTDDMIQESVARAEQSGIIFIDEIDKVASQGKGSGPDVSREGVQRDILPIVEGSTVMTKYGPVKTDYVLFIAAGAFHIAKPSDLIPELQGRFPIRVELSSLTLEDFVSILTEPENALTKQYVHLLQTENIEIQFQKEAIQEIAKIAASVNQNMENIGARRLHTILEKLLEDLSFEAPELTLETMVITPEYVREKLAGIAQDRDLSQYIL
>NZ_CP009285.1|WP_042214906.1|4930004_4930412_-|flagellar-basal-body-rod-protein-FlgB
MGLLNSVSFQRLQGGLDAATKRQSVLANNVANVDTPNFKRSDVSFESFLRQQENGLKPTLSAKVSDSRHFQFGTVTGVPAAVVSTDETTSMNNNGNNVDMDREQALSAENQLRYNSYVEQLNSQITMMRTVVQGG
>NZ_CP009285.1|WP_042214904.1|4929551_4929998_-|flagellar-basal-body-rod-protein-FlgC
MNFGSSFGISASALTAQRLRMDVISSNIANAETTRASVVDGKAVPYRRKLVVLETAQADSFSNILDSKMSGGSEGVKVKSIIEDSSPLKPVYNPSHPDADVDGYVYMPNVDLTKEMVDMLSASRSYEANVTMLNASKAMVGKALEIGR
>NZ_CP009285.1|WP_042214902.1|4929214_4929523_-|flagellar-hook-basal-body-complex-protein-FliE
MIQNLLIGTQAVQPLAMKTPAAETSAVSGTGQSFGSYLENALNQVADQEQQAKDMSNKFVLGEVNIDEAMISSQQALLSLQLTTQVRNKVIEAYQEIMRTQI
>NZ_CP009285.1|WP_042214899.1|4927590_4929180_-|flagellar-M-ring-protein-FliF
MNERLAQYREKISQYWNRFSGKQKILFFSTLFIIIIIIVVLTMQLSKTEYEVAFQDLDSTDSAGVMSYLDTAGIAYRLSPDGKSISVPSTDAARIKVDIGSQGIVQGGSIGYKVFDESSSMIGTTDSEFNVKYNNALNGEVEQLMRRMQGIKDVKVLITLPKETVFASQEDQEKAQASVVLSFDPGFRPSQENIDGYFNLVKTAVPNLPVENITITNNEVELMPTAKGGQAGVSSQVEENFALQKKFEDDVKKDVKQFLSTLTGPDKVDVLVFSKLNFDKENRQEEIVLPVDAENMKGIEISSQIISNTYSGQGNTSGGVAGTGSEDVSGYPSGTDSGTSSSEESSETRNYEVNRISKDIIASPYTVKDLTINVAVEPPDGQTTLDDTTSAAIQNILVNIVRASLADSGLTYTDADLTKKVSVFSQQFGSTAANAASGGLATWMIWAIGGAALLVGAGGGYLIYRSRKNKQEEEAEDDIPLQVPTEFPSINMDSVTNESQVRKQLESLAKKKPDEFVNLLRTWLAEEQR
>NZ_CP009285.1|WP_042138160.1|4926569_4927586_-|flagellar-motor-switch-protein-FliG
MAKASQQGLSGRQKAAILLITLGPEVSAQIFKHLRDEEIEQLTLEIANVRKVDSVEKESIMSEFHQICLAQEYISQGGINYAKEILEKALGSAKALEVINRLTATLQVRPFDFARKADPNQILNFIQNENVQTIALVLSYLQFEQAASILSSLPQEKQAEVARRIAIMDSTSPEVVTQIERVLEQKLSATVTQDYTNAGGIESIVQILNGVDRGTERTILDSLEIQDPELAEEIKKRMFVFEDIVNVDNRSIQRIIKDIDNADLQLALKVASEEVRDVIFRNMSKRMAETFREEMEYMGPVRLRDVEEAQTRIVGTIRRLEESGEIIIARGGGDDIIV
>NZ_CP009285.1|WP_042214896.1|4925728_4926577_-|flagellar-biosynthesis-protein
MSKLIKHSQYVPVDVLKRLEQARHHAGLTEDPVVEEAPGEVHYQDPAREAAEQARKQMLKDAQEFAEGQVRSASQEAENIMESARNEAEEWWRQRREQDEHLVEAVKSEGFQQGYQEGLAHAEQEMSQRLAEMMEEARTVLQEAYRARDVIIQEAEPFLVELSCDIAEKIVDKQLTVEPQFAMDLIRKNLARKREQGLISLCVSPAQFAFVNAAREELSLAVDSQAELQILPDSTVKDQGCVIRSSFGSIDARVDTQLAEIKKELLRIALDAGEHGSGEDDA
>NZ_CP009285.1|WP_042214893.1|4924422_4925736_-|flagellar-protein-export-ATPase-FliI
MLDSGRYKEQLRNFDPVRINGKVTQVIGLMVESEGPDASIGDVCFIYPAKGTKPLQAEVVGFRDNKVLLMPLGELQAIGPGCDVVGTGKPLSVQVGSELLGKVLDGLGQPLDGSLIPARMPHSSTFNIPSNPLNRPRVAEPISIGVRAIDGLLTIGKGQRVGIFAGSGVGKSTLMGMIARNTSADVNVIALIGERGREVLDFIERDLGPEGLQRSVVIVATSDQPALIRIKGALIATTIAEYFRDRGLNVMLMMDSVTRYAMAQREVGLAVGEPPAMRGYTPSVFASLPKLLERAGTGPTGSITAFYTVLVDGDDMNEPIADAVRGILDGHIVLNRNIANKGHFPAIDVLSSISRVMKDIAPEEQIAAAENVKRLMAVYKDSEDLINIGAYQRGSNAQIDESIHYIDSIWDFTKQKVNEKVTLSEVQQSLISQFSRS
>NZ_CP009285.1|WP_042214890.1|4923972_4924416_-|flagellar-export-protein-FliJ
MRFHYTFQKVVDLKGNEKTQAEWMLSSALGELQAQEKSLDELITQRSALMSSLQSAAEQRTPLAKLREMQDYVDYLDKCIARKHSDISRAHIEVQSKQDHLSTKVLDEKVWLKAKDKAQTAFLQNMSLREQNELDEMATVRFAMKSL
>NZ_CP009285.1|WP_042214912.1|4932912_4934292_-|FADH(2)-oxidizing-methylenetetrahydrofolate--tRNA-(uracil(54)-C(5))--methyltransferase-TrmFO
MTDIAKVTVIGAGLAGSEAAWQIASRGVPVRLYEMRPVVKTPAHHTDQFAELVCSNSLRANGLGNAVGVLKEEMRRLDSLVLGAADRHAVPAGGALAVDRDGFSGEITSMLHNHPLVEVINEELTHIPEEGIVVIATGPLTSPALSAEIKGLLGEEYFYFYDAAAPIVEKDTIDMSKVYLASRYDKGEAAYLNCPMTEEEFDVFYDALISAETAALKDFEKEIYFEGCMPIEIMMKRGKQTALFGPMKPVGLMNPHTGKLPYAVVQLRQDNAAGTLYNLVGFQTHLKWGEQKRVFSLIPGLENAEYVRYGVMHRNTFINSPKLLHPTYQMKGRERLFFAGQMTGVEGYVESAASGMIAGMNAARAALGEDGLIFPQDTVLGSMPAYITSADSEHFQPMNANFGLLPKLETRFRSKKEKNERLAYRALDSLAAYAAAKGLAYTEPEVVEPGLTEAESPAQ
>NZ_CP009285.1|WP_042214914.1|4934315_4936412_-|type-I-DNA-topoisomerase
MADALVIVESPAKAKTIGKYLGSKYIVKASMGHIRDLPKSQIGVEVENDFNPKYITIRGKGSILKELKDASKKVKKVYLAADPDREGEAIAWHLAHALDLDNTQECRVVFNEITKQAVKDAFKTPRKINMDLVNAQQARRILDRLVGYKISPLLWKKVKKGLSAGRVQSVAVKIIMDRENEISAFVPTEYWSITAKLGIRDSLFEAKFHKLNGDKKELGQESDVQEVLEAIKNAAFQVKEVKEKERQRHPSAPFTTSSLQQEAARKLGFRASKTMSVAQQLYEGVELGKEGTVGLITYMRTDSTRLSVTAQEEAKELILSKYGEKFVPETPRQYSKKAAGAQDAHEAIRPTSALREPDMVKEFLSRDQFRLYKLVWERFVSSQMSSALLDTLSVDITAGTAIFRAVGSKVSFPGFMKVYVEGNDDGTTDEEKYLPPLKAGDDLIKHDIEPKQHFTQPPPRYTEARLVKTLEELGIGRPSTYAPTLETIQKRGYVAIEEKKFMPTELGELIIEQMEEFFPEILDVEFTAHMEGDLDHVEEGAEDWVKVLAQFYESFEKRLLYAEEEMKEIEIEDEVSDELCEKCGKPMVYKLGRFGKFLACSGFPDCRNTKPIIKDIGVSCPKCHEGKVVERRSKKGRVFYGCDQYPGCDFVSWDRPSVKPCPVCGSWMVEKRNKQGTKLQCTSCDHTEAVLDNEELAE
>NZ_CP009285.1|WP_174479825.1|4936510_4937629_-|DNA-protecting-protein-DprA
METRDLLFGLNEVEGIGWKSIDRIRQAGLLTNEALSCSASDWERAGISGKMSARLSAVFNEEWILGRRSLMEESGALMVTFLDESYPVQLKETPQPPWVLYYRGRLELASRPSVAMVGTRVPTAYGRKIGEMLAGQLSAAGLTVVSGLARGIDSVCHEAALTGTGSTIAVVATGLDKVYPPENRELERQISRVGLVLSEYPIGTPSHPGLFPQRNRIIAGLSLGTVVVEADSRSGSLITADAALEAGRDVFAVPGPLTSPKSRGALELIKQGAKLVTSSTDIVEEYIAYLPAKGSAGPPASGSGPSGGDGLIEKKLTSEELHLYHILHQGPFTLDELLASTRWDFGHLHSVLLSLIIKKAVTQLPGAIYKVI
>NZ_CP009285.1|WP_039295139.1|4937812_4938742_-|succinate--CoA-ligase-subunit-alpha
MSILVDKHTKVITQGITGATGLFHTKGALDYGTQMVGGVTPGKGGTFVQITLENGTEASLPVFDTVVAAKAATGATASVIYVPPAFAADSIMEAVDAEMELVICITEGIPVLDMVKVSRYMEGRSTVLIGPNCPGVITPGECKIGIMPGYIHMPGYVGVVSRSGTLTYEAVHQLTERGIGQSSAVGIGGDPVKGSEFIDILKLFNDDPGTKAVIMIGEIGGTAEEEAALWIKENMTKPVVGFIGGVTAPPGKRMGHAGAIISGGKGTASEKIAVLESCGIKVAPTPAEMGSTLVSVLEERGILNAFTTH
>NZ_CP009285.1|WP_042214918.1|4938777_4939935_-|ADP-forming-succinate--CoA-ligase-subunit-beta
MNIHEYQGKEVLKKYGVAVPNGKVAYTVEEAVEAAAALSTPVVVVKAQIHAGGRGKAGGVKVAKNSDEVRAYAAEILGKTLITHQTGPEGKVVKRLLIEEGCQIVKEYYIGLVVDRGSGRVVMMASEEGGTEIEEVAATHPEKIFKEIIDPAVGLQTFQARKLAYSIAIPSELVNKAVKFMQALYLAFVDKDCSIAEINPLVVTADGNVMALDAKLNFDSNALFRHKDILELRDLDEEDAKEIEASKYDLSYIALDGNIGCMVNGAGLAMATMDIIKYYGGEPANFLDVGGGATTEKVTEAFKIILSDDKVSGIFVNIFGGIMRCDVIATGVVEAARQLGLTKPLVVRLEGTNVALGKEILAGSGLNIVAADSMADGARKIVALV
>NZ_CP009285.1|WP_042214920.1|4940293_4940761_-|MarR-family-transcriptional-regulator
MQEETMTPPELMLENQLCFTIYACSREFTKLYQPHLDKIGLTYSQYLVMLVLWERRQCTVKELGEALFLDSGTLTPLLKRLQAAGLILRERSLQDERKVLISLTAQGLALQQDAMCIPGKMAEGTMLSPEEFIGLLGQFKDLLARVHESNISNSK
>NZ_CP009285.1|WP_042214922.1|4940909_4941338_+|organic-hydroperoxide-resistance-protein
MMTIQQKMYETTVKAVGGRQGYIESESPKLNLTISTPREMGGAGGEGTNPEQLFAAGYSACFDSALNMVARMGKIKIEGSEVTATVSFGKVEDGGFGIAVKMDVLVKGVDHETAVQLVEAAHGACPYSRATRGNIEVELNVL
>NZ_CP009285.1|WP_042214925.1|4941505_4943233_-|YifB-family-Mg-chelatase-like-AAA-ATPase
MYGKMHSACLYGIEGVMIGVEIDLANGLPQTIIIGLPDSAVREAVERVRAAVKNCGYSYPQQRVTINLAPADLRKEGSAFDLAIALGILTTSGQLVMPDAEKMLLIGELALDGSLRPVNGVLSMVEAARRAGFQAVLVPPGNAAEAALITGIRVYTAGHLRELSPSAASVPASPVTVEPVPVLELPIATEVPDSAIPKLSMLQTELPFPVSVSKEPSPRNRPPVQVLTLDHLRYQPEGDKILAPSREDHLMKEDYSDVIGQNHVKRALTIAAAGMHNIILIGPPGTGKTMLIKRLPGILPDLSDDESLEVMKIFSAAGKLRDSNGGLMRLRPFRSPHHTISAAGLIGGGGIPKPGEVSLAHRGILFLDELPEFSRTVLEVLRQPLEDGVVTISRARASFTFPAQFLLACSMNPCMCGFLGNGSSQQRCTCSPARIAQYRAKISGPLLDRMDMQVDVPRPKEWDRNVPALSTAQMREDVLRAQAIQAKRYQRLPISWNSELSGAALRRYAALRHEENLLLNSILESLGLSMRAHDRIIKLARTIADLEGAEEINSAHLAEAVQYRNLDRQVLTEEE
>NZ_CP009285.1|WP_042214927.1|4943445_4943955_-|metallophosphoesterase
MSSVFFTSDHHFGHKLIIDFESRPFDSAEEMDRSMIASWNAVVGNGDTVFHLGDFSFLNQEATRTIISALNGYKILILGNHDRGRGRDWWLKAGFDEVSEYPLIYKEFFMLSHEPLYMNKHMPYVNVHGHIHGQKYEGKSHFNICVEHWNYMPLSFEQIRDAVVASEEG
>NZ_CP009285.1|WP_052429577.1|4943989_4944403_-|hypothetical-protein
MRNQPIDIQVSFTCQHCEHRVVAELGGEPLSVVCCSNCNKTFTVMRPAIAEEILIDWEHEALFHKMRAEKTESSNSSLLSLVINVIELLTWKDKGNGQVEAIKEMRQWLIDHEEAPPLAELIQVDVNRRSSKRNWNK

Crispr_ID: NZ_CP009285_14

• CRISPR_ID: NZ_CP009285_14
• CRISPR_location: 5378112-5378185
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_14

Consensus_repeat	Method
ATAAGGGAATCTCAGTCCGTTTCA	CRISPRCasFinder

spacers of NZ_CP009285_14

>14.1|5378136|26|NZ_CP009285|CRISPRCasFinder
GCTGCAAAAGGAGGCTTTTGGGCGAA

CRISPR arrays and Neighbor proteins around NZ_CP009285_14

CRISPR arrays

The CRISPR arrays of NZ_CP009285_14

>merge|NZ_CP009285|14|5378112-5378185|CRISPRCasFinder
ATAAGGGAATCTCAGTCCGTTTCAGCTGCAAAAGGAGGCTTTTGGGCGAAATAAGGGAATCTCAGTCCGATTCA

>NZ_CP009285|14|13|5378112-5378185|CRISPRCasFinder
ATAAGGGAATCTCAGTCCGTTTCA	GCTGCAAAAGGAGGCTTTTGGGCGAA
ATAAGGGAATCTCAGTCCGATTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042215667.1|5368561_5369620_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|376439
NZ_CP009285.1|WP_042215675.1|5373271_5374207_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381312
NZ_CP009285.1|WP_042215683.1|5379373_5379829_-|anti-sigma-F-factor	unknown	unknown	gnl|CDD|179626
NZ_CP009285.1|WP_099052486.1|5380365_5381598_-|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl|CDD|224600
NZ_CP009285.1|WP_042215671.1|5370673_5372368_-|oleate-hydratase	unknown	unknown	gnl|CDD|237575
NZ_CP009285.1|WP_042215688.1|5383563_5384526_-|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|236898
NZ_CP009285.1|WP_052429607.1|5381739_5382165_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215680.1|5375138_5376734_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_CP009285.1|WP_042215690.1|5384522_5385500_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_CP009285.1|WP_042215691.1|5385537_5386821_-|ArgE/DapE-family-deacylase	unknown	unknown	gnl|CDD|349933
NZ_CP009285.1|WP_042215686.1|5382263_5383292_-|acyltransferase-family-protein	unknown	unknown	gnl|CDD|226122
NZ_CP009285.1|WP_036727462.1|5379825_5380179_-|anti-sigma-F-factor-antagonist	unknown	unknown	gnl|CDD|131932
NZ_CP009285.1|WP_042215681.1|5377316_5377871_-|RNA-2'-phosphotransferase	unknown	unknown	gnl|CDD|179136
NZ_CP009285.1|WP_039300284.1|5378606_5379362_-|RNA-polymerase-sporulation-sigma-factor-SigF	unknown	unknown	gnl|CDD|180137
NZ_CP009285.1|WP_174479828.1|5387038_5388643_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173877
NZ_CP009285.1|WP_042215673.1|5372503_5373118_-|TetR-family-transcriptional-regulator-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|379534
NZ_CP009285.1|WP_042215668.1|5369871_5370183_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215664.1|5367524_5368559_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|376439
NZ_CP009285.1|WP_039300264.1|5370306_5370528_-|hypothetical-protein	unknown	unknown	gnl|CDD|319771
NZ_CP009285.1|WP_042215677.1|5374220_5374961_-|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|277316

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042215667.1|5368561_5369620_-|iron-ABC-transporter-permease	gnl|CDD|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	2.48892e-85
NZ_CP009285.1|WP_042215675.1|5373271_5374207_+|aldo/keto-reductase	gnl|CDD|381312	cd19086, AKR_AKR11C1, AKR11C family of aldo-keto reductase (AKR). Bacillus subtilis uncharacterized oxidoreductase YqkF is a founding member of aldo-keto reductase family 11 member C1 (AKR11C1). It may function as oxidoreductase. This family also includes Bacillus halodurans AKR11C1, an NADPH-dependent 4-hydroxy-2,3-trans-nonenal reductase.	6.9233e-101
NZ_CP009285.1|WP_042215683.1|5379373_5379829_-|anti-sigma-F-factor	gnl|CDD|179626	PRK03660, PRK03660, anti-sigma F factor; Provisional.	1.10443e-82
NZ_CP009285.1|WP_099052486.1|5380365_5381598_-|D-alanyl-D-alanine-carboxypeptidase	gnl|CDD|224600	COG1686, DacC, D-alanyl-D-alanine carboxypeptidase [Cell envelope biogenesis, outer membrane].	7.44598e-117
NZ_CP009285.1|WP_042215671.1|5370673_5372368_-|oleate-hydratase	gnl|CDD|237575	PRK13977, PRK13977, myosin-cross-reactive antigen; Provisional.	0
NZ_CP009285.1|WP_042215688.1|5383563_5384526_-|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	8.58472e-168
NZ_CP009285.1|WP_042215680.1|5375138_5376734_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	1.2726e-30
NZ_CP009285.1|WP_042215691.1|5385537_5386821_-|ArgE/DapE-family-deacylase	gnl|CDD|349933	cd08011, M20_ArgE_DapE-like, M20 Peptidases with similarity to acetylornithine deacetylases and succinyl-diaminopimelate desuccinylases. Peptidase M20 family, uncharacterized protein subfamily with similarity to acetylornithine deacetylase/succinyl-diaminopimelate desuccinylase (ArgE/DapE) subfamily. This group includes the hypothetical protein ygeY from Escherichia coli, a putative deacetylase, but many in this subfamily are classified as unassigned peptidases. ArgE/DapE enzymes catalyze analogous reactions and share a common activator, the metal ion (usually Co2+ or Zn2+). ArgE catalyzes a broad range of substrates, including N-acetylornithine, alpha-N-acetylmethionine and alpha-N-formylmethionine, while DapE catalyzes the hydrolysis of N-succinyl-L,L-diaminopimelate (L,L-SDAP) to L,L-diaminopimelate and succinate. Proteins in this subfamily are mostly archaeal, and have been inferred by homology as being related to both ArgE and DapE.	6.43841e-97
NZ_CP009285.1|WP_042215686.1|5382263_5383292_-|acyltransferase-family-protein	gnl|CDD|226122	COG3594, NolL, Fucose 4-O-acetylase and related acetyltransferases [Carbohydrate transport and metabolism].	3.31846e-17
NZ_CP009285.1|WP_036727462.1|5379825_5380179_-|anti-sigma-F-factor-antagonist	gnl|CDD|131932	TIGR02886, Anti-sigma_F_factor_antagonist, anti-sigma F factor antagonist. The anti-sigma F factor antagonist, also called stage II sporulation protein AA, is a protein universal among endospore-forming bacteria, all of which belong to the Firmcutes [Regulatory functions, Protein interactions, Cellular processes, Sporulation and germination].	1.69385e-50
NZ_CP009285.1|WP_042215681.1|5377316_5377871_-|RNA-2'-phosphotransferase	gnl|CDD|179136	PRK00819, PRK00819, RNA 2'-phosphotransferase; Reviewed.	1.38978e-66
NZ_CP009285.1|WP_039300284.1|5378606_5379362_-|RNA-polymerase-sporulation-sigma-factor-SigF	gnl|CDD|180137	PRK05572, PRK05572, RNA polymerase sporulation sigma factor, SigF/SigG family.	4.49686e-167
NZ_CP009285.1|WP_174479828.1|5387038_5388643_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173877	cd08512, PBP2_NikA_DppA_OppA_like_7, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	2.12791e-166
NZ_CP009285.1|WP_042215673.1|5372503_5373118_-|TetR-family-transcriptional-regulator-C-terminal-domain-containing-protein	gnl|CDD|379534	pfam14278, TetR_C_8, Transcriptional regulator C-terminal region. This domain is a tetracycline repressor, domain 2, or C-terminus.	1.69333e-23
NZ_CP009285.1|WP_042215690.1|5384522_5385500_-|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0
NZ_CP009285.1|WP_042215664.1|5367524_5368559_-|iron-ABC-transporter-permease	gnl|CDD|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	5.69122e-92
NZ_CP009285.1|WP_039300264.1|5370306_5370528_-|hypothetical-protein	gnl|CDD|319771	cd02076, P-type_ATPase_H, plant and fungal plasma membrane H(+)-ATPases, and related bacterial and archaeal putative H(+)-ATPases. This subfamily includes eukaryotic plasma membrane H(+)-ATPase which transports H(+) from the cytosol to the extracellular space, thus energizing the plasma membrane for the uptake of ions and nutrients, and is expressed in plants and fungi. This H(+)-ATPase consists of four domains: a transmembrane domain and three cytosolic domains: nucleotide-binding domain, phosphorylation domain and actuator domain, and belongs to the P-type ATPase type III subfamily. This subfamily also includes the putative P-type H(+)-ATPase, MJ1226p of the anaerobic hyperthermophilic archaea Methanococcus jannaschii. The P-type ATPases, are a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0.00484144
NZ_CP009285.1|WP_042215677.1|5374220_5374961_-|serine/threonine-protein-phosphatase	gnl|CDD|277316	cd00144, MPP_PPP_family, phosphoprotein phosphatases of the metallophosphatase superfamily, metallophosphatase domain. The PPP (phosphoprotein phosphatase) family is one of two known protein phosphatase families specific for serine and threonine. This family includes: PP1, PP2A, PP2B (calcineurin), PP4, PP5, PP6, PP7, Bsu1, RdgC, PrpE, PrpA/PrpB, and ApA4 hydrolase. The PPP catalytic domain is defined by three conserved motifs (-GDXHG-, -GDXVDRG- and -GNHE-). The PPP enzyme family is ancient with members found in all eukaryotes, and in most bacterial and archeal genomes. Dephosphorylation of phosphoserines and phosphothreonines on target proteins plays a central role in the regulation of many cellular processes. PPPs belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	4.23388e-30

Protein sequences

>NZ_CP009285.1|WP_042215681.1|5377316_5377871_-|RNA-2'-phosphotransferase
MDYSKLSKEVSYALRHAPWEYELELDEEGFVEIEQLLNALHLEHQWNSVTAADLAKMIEASAKQRHEIVEGKIRALYGHSVPQKIIKKDEIPPPILYHGTARQWVETILTDGLKPMKRQYVHFSVDTETAKLVGGRKDINPVILTIDAGRAAHEGIKFYHGNHNIWLADYIPPEFIAKDIFSSE
>NZ_CP009285.1|WP_042215680.1|5375138_5376734_-|sigma-70-family-RNA-polymerase-sigma-factor
MLQWIEEAQKGDAEAFRQLTEHVRGMAYVVSYDMLGDVQLAEDAVQEAFIDAYMNLGSLQEPAAFPGWFRTIVVRQCHRLLRRRRQTLLPLEAAEHVAGSTPGVEEIAEHRERARVLHSSVAKLSAKLRVPVQLFYFYGYSLQEISVYMGIPAGTLKKRLYDGRRKLQGAYPVADLAAAMNLLHEGGQRMLHIVNGDSVGDKLKQGIVQGDVLVWREIYTAGPIFIDPAAPKERQLRAEVLQATLGIPATEFIAGCEEQERILSGFHRYDEVVLWFEHDLFDQSMLAYLLHWFSMQKPDSTKLSLLCIGEFPGIELFHGLGQLTAAQLQTLSGTWQNIGTEELELGSRLWQAYASPDPRQLAALLEESKPQLAGSALSFAYDAFKAHLSRLPSVDNGLGIVEQTTLKAAAGGADTPLKLFRQVTDSLHRLGMGDVEYWKYLRTLTAGEHPLLTIEGTAETTDYRQVPEFLNRTVILTELGEQVLAGTADRVTLQGIDEWYGGLHQQGHDVPWRWDNAAELPVRVHNVTQSE
>NZ_CP009285.1|WP_042215677.1|5374220_5374961_-|serine/threonine-protein-phosphatase
MRTLVISDIHGCVEEFNLLLRRASYIPSEDQLILLGDYVDRGPDSRAVVEQVKRLAEESGAVVLRGNHDQMACDALTGEDDKRDTHWITNGGFHTLLSYCGGCDSVLLRPDSGWKDYAEMKEYMRQEYKEHLDFLGTLPFYYETDTHLFVHAGIDPSLANWTSQREYDFIWIREPFYNYPVTSTAKTVVFGHTSTVDLQDGAGIWFSPHGDKIGIDGGCVYGGQLNCLEINDDGYKTYSVRLGEKE
>NZ_CP009285.1|WP_042215675.1|5373271_5374207_+|aldo/keto-reductase
MNRRRYGSTGKTVSEIGFGAWQLGNKQDWEAMEDRAAVSLVHEALERGMNFFDTAPGYGGGASETLLGAALSGRRAGAVINTKFGHGADGSTSFDTDHIRASIEGSLQRLQTDYVDSVLIHNPPFELLDGKFGHYHELDKLKSEGKILSYGVSVDSVPEMLEVIRHTDIGVMEVMFNIFYQETAEAFKLAHEKDIALIVKVPLDSGWLSGKYDSSSTFEGVRSRWSPEVIAKRAALVDRIRFITDEETTMTMAALRFILAHPEVTTVIPGVRSSAQLAENISASHEVMPPEHVVRLKELWDKEIRDQQLGW
>NZ_CP009285.1|WP_042215673.1|5372503_5373118_-|TetR-family-transcriptional-regulator-C-terminal-domain-containing-protein
MSNSLLTKNALARSLKKLMLARPLNKITIQQLTADCGVTRHTFYNHFQDIYELLGWVYRSEVIEGLEPYRCCAGWKQGFLSVLRYTVSNKTICLNTFHSLGREHLEDFLYGVIYGVIIRVVEELDGQELDREGQRQIPEPVKKQARHEIADFYTLAILEQVIHWLKAGANTDPAEIVEKVARIMDGSIARSLEHYQSAAAHPVK
>NZ_CP009285.1|WP_042215671.1|5370673_5372368_-|oleate-hydratase
MGTYQRIHPLVQEGIASRKAYLIGGGIGSLSAAAFLIRDGHMPGRNIHILEQSAIYGGSMDGAGNAKDGYSARGGREIEEHFECFMELFGFIPSLTNPDRTVLDEFRELNLAEPIESHCRLVEKEGQPADFSTLGLSTAHALQLGKLTLATEERLGAVTIEQFFDPTFLETNFWYFWRSMFAFENWHSVVEVKRYMERFMHLISGMNQLKGILHTEYNQFDSLILPLMKWLESQGVNFDKGHQVTDLELDFTGGEKTVTAIQLLVNGSPKTISTARGDLVMVTNGSMTENSTLGDLDHPAILNRSVTERGCWSLWEKLAAKSPDFGHPEVFCGDIDKSKWLSFTMTFTDDDIVFPYLLELTGDAPGMGGVVTIKDSNWMMSWTAPKQPHFINQPDNVKVLWAYGLFPDAEGNYIKKKMSDCTGRELLEELMYHIGLKNRIPEILEHTTNVIPCMMPYITSQFMPRVAGDRPQVVPQGSTNLAFLGQFAEVPDDCVFTVEYSVRSAMMAVYNLLALEKEVIPIHPSKYDVRVLLTALRTCLGNKPLPLDKTLGQLLAGTVISKLL
>NZ_CP009285.1|WP_039300264.1|5370306_5370528_-|hypothetical-protein
MRKILSRIGLGLLLLIIAAVVLCFYFNQFTYAYTLLVVLLFIFGGMGQMYKLKNDEYMYSRHNQKDEYEEYTR
>NZ_CP009285.1|WP_042215668.1|5369871_5370183_-|hypothetical-protein
MNERLAALILRIDAIATDIIVPLRRKSINEAALLQLYEALDETYLLIEHEKQIDRELAAILFLIYSQLVSQSNYVYDKSNFVPHIGKLQGYIRRLFGGTLQNV
>NZ_CP009285.1|WP_042215667.1|5368561_5369620_-|iron-ABC-transporter-permease
MNQQAVSRNGLDQRAEPLKLRSRPWAATLILIGGLIALALGIAVSVSFGAADIKLSVVWTAVFHFNPDITEHQIIRELRLPRVLGGVMVGASFAVAGAIMQGMTRNPLADSGLMGINSGAGFALAVCFAFFPNLSFMYLILYSFIGAGAGAGIVYGIGSLAKGGLTPARLVLAGAAFSALLSALSEGVALYFKIGQDLAFWYAGGLAGTKWFQLQVMSPWVIAAIIGAIVLSRSITMLSLGEDIARGLGQRTGLVKLAGALIVLILAGASVAVVGAVGFVGLIIPHLTRYLVGVDYRWIIPCSAVLGALLVVGADLTARMINPPHETPVGAIISLIGVPFFLYLARKERREL
>NZ_CP009285.1|WP_042215664.1|5367524_5368559_-|iron-ABC-transporter-permease
MQRTKVISFEEARRKHGLNVLGVLAALIVIMFIISVNTGYIRLTPLELLNTLFGKGTDKQELILFQFRLPRIVISILIGAALAVSGAVMQGVFRNDLADPGILGINAGAGLMVMLMVSFYPTTSAAPVYLLPVVAFVGAAFTAALIYSLAYKRHQGIAPIRLLLTGVAVAAGMSAAMIVLTLRLDPDKYQFVATWLAGSIWGTSWKFVLSLLPWIVILLPYVIYKARVMNVLNLGEQTATGLGAHVTREQFRLLAAAVGLAASSVAVSGGIGFVGLVGPHLARRLVGPKHQLMLPASALLGALLVITADTIGRRILQPSEIPTGIVVAVIGAPYFLYLLARTKS
>NZ_CP009285.1|WP_039300284.1|5378606_5379362_-|RNA-polymerase-sporulation-sigma-factor-SigF
MDAESKKAPPTYLDDAEVKRLIALSQAGDNTARDTLVNCNIRLVWSVVQRFMNRGYEPDDLFQIGCIGLLKSVDKFDLSYEVKFSTYAVPMIIGEIQRFLRDDGTLKVSRSLKEMANKVRKMKDEMSKTLDRLPTIGEVAEALGVTPEEIVFAQEANKPPTSIHETVFENDGDPITLIDQIADESQERWFDKLALNEAIGALTERERLIVYLRYYRDQTQSEVASRLGISQVQVSRLEKKILANIREQIAQ
>NZ_CP009285.1|WP_042215683.1|5379373_5379829_-|anti-sigma-F-factor
MTNSEARNFMSVQFAALSENESFARVVVAAFVSRLDPTMEELNDLKTVVSEAVTNCIIHGYDSDPAGVVSISASIDFETVHLTIEDQGRGIEDLELAQQPLYTSKPELERSGMGFTIMENFMDEFEVTSEPGRGTSISMKKTIVSKKALYN
>NZ_CP009285.1|WP_036727462.1|5379825_5380179_-|anti-sigma-F-factor-antagonist
MNSHVEMEHHRGVLIVRLSGELDHHAADYVRMDMDEAIMRGQVEHLILSLKELQFMDSSGLGVILGRYKLIRSKGGKMAVCDATAPVKRLLEMSGLFKIMPLYDDESAALSDLEVAL
>NZ_CP009285.1|WP_099052486.1|5380365_5381598_-|D-alanyl-D-alanine-carboxypeptidase
MFRRGTIVRKIRYVTLALCIAVSVLGGASGAFAEEKAKGTANTGNTGSIAAADLAPGARSAILMDASTGTIIYEKNSHDKLPPASITKIMTMLLTVEALDEGRLQLTDKVRTSEYAASMGGSQIFLEPGEEMTVDEMLKGIAMASGNDASVAMAEKIAGSESAFVDLMNQKAEALGLKDTHFANCNGLPAANHYSSAHDIAVISQELLKHERIIKYTGSYQDYLRKDSAKPFWLVNTNKLVRFYTGADGLKTGYTAEAKFCLSATAARDGLRAVAVVLGEPNTKTRNSEVSAMFDYLFSQYKLHTIHKAGDTIGTVKIEKGVKTELPLTAKETYSVLLKKGITQEGIRHELVLEENLKAPVAADQTVGKLVVYQGTDVLKEYELKAGEDVAKAGWWKLFKRTTGSLFTID
>NZ_CP009285.1|WP_052429607.1|5381739_5382165_-|hypothetical-protein
MVKTLLDYNASVVTPITNGVAIPVPISPAGVQIAGTSVYIDPAVPAHFPNKVELKATIGVNVTLDTPNILVRIWRAGFEIFYARAEYEDFFNDDGIISLHMVDINVPAGVQNYQLIVENQDTNSTAVVVGPVIFSAMAIGG
>NZ_CP009285.1|WP_042215686.1|5382263_5383292_-|acyltransferase-family-protein
MEKRRELWIDAAKGFSIIFVVMGHSGDAAANHYLSWFRMPLFFQLSGLVFKPVDPGRYLGWAARRTKGLMTPYFAYGLLIAVVLLLFSFNIRGFAENMARLLYGGLSLTGPYGVFWFITCLLFTQLLFGYIVRYSRRIQLLLLTSAYLVSHLISLTALKNFNLPWNIDVALLAVTYYAIGFYGKQAIPALISRYSALLVLLPLSALVLLLERTGIIHYSLNMKYKEYESLLLDLAVPLLISLTICAAVYQLARLIPLGWMGSLGRNTITIMYLHLPLNYSLKYLLGADYGLVPFTLIGVIVPLLAAKWAVRYPVLSRFYLGKAGGVPPAKRTGKAASVSSNG
>NZ_CP009285.1|WP_042215688.1|5383563_5384526_-|dipeptide-ABC-transporter-ATP-binding-protein
MSTILEVRNLKKHYPIRKGFFSKQVGAVKAVDGITLSVQQGETLAVVGESGCGKSTTGRAILRLIEPTEGEIMFNGTDVRALSTEQLRRFRTDMQMVFQDPYASLDPRWTVQRILEEPLRTHESAPASELKSRVEQLMEVVGLSPYQAHRFPHEFSGGQRQRIGIARALALNPKFIVCDEPVSALDVSIQAQVLNLMQDLQEQYGLTYMFISHDLSVVKFISDRVAVMYLGRIVELAPTRSLFAKPLHPYTQALMSAVPVPNPGVKKQRIVLTGDVPNPETPPSGCAFHPRCPYAMDRCKSEAPVLRELDSGHQVSCHLY
>NZ_CP009285.1|WP_042215690.1|5384522_5385500_-|ABC-transporter-ATP-binding-protein
MTELLEVSGLCTEFQTAAGTIRAVDGISLSVRKGETLGIVGESGCGKSITSLSIMQLLPKRISRIASGHIRFEGKDMLEMSMKEVRGIRGNRIAMIFQEPMTSLNPVFKIGRQISESARYHLKLSKKEAAERAVEMLRKVGIPRPEKIAQQYAHQLSGGMRQRVMIAMAMVCNPQLLIADEPTTALDVTIQAQILDLMRELQEKEGMSILMITHDLGVVAEMCDRVVIMYAGQIVEETDVATLYSNPLHPYTRGLLASLPQLAGDEDRLSSIPGQVPNPANLPSGCRFAPRCPVAVERCSEKLPELLEVQPGHTCRCILQQEGVI
>NZ_CP009285.1|WP_042215691.1|5385537_5386821_-|ArgE/DapE-family-deacylase
MTDWKSKVLEAIDAEQDKLLELCSQLIRFPSENPPGDSREISAFIIDYLKEAGIDTRVHPATDTMLNLVSTLGTGSELPSGKNLIFCGHTDVVPAGDRSRWDFDPFSGDIVDGYLLGRGASDMKAGLAGLIYVTALLSKLGVPLKGDLSLLIVPDEETGGHLGVPWVLERGLITGTAAVIAEPSGPLNPTIGQKGSCWFEFTVEGTPGHGSLSPVVGDSAIVKAAKGIEALQRLWDIKVDIPDEVKEIIRISQDYVKEREQDGSIAYQVFDHVTVNIGTIQGGTKVNVVADRCTIQVDSRVPFGVDYRDVLDRARSLLLEAGIESEVKGFGFQGNANWTSNEEPVVSDLVESICEVSGEEAYGVLQWASSDARHFRTHNIPVLQYGPAELSTIHNFNEKAPVWQIIQCAKVYALTALKYLGVEDTEN
>NZ_CP009285.1|WP_174479828.1|5387038_5388643_-|ABC-transporter-substrate-binding-protein
MKRVKLLSTLVAFSVMLAGCASSANPQTPAATTAASGTTGTAAPAAKSNLTVAYSEGGTTLDPAEANDLTSDTLVLAAYDQLVTYGIKTENGTSIANTEDIQPMLAESWEVNADNTVYTFKLKSGVSFQSGNPVDAEAVAYSFDRVAKSSSGSFLYGMAAIKSVAVKDASTVEVTLTNANHNFLQILAMYTFSIVDQKTVEAQGADYLKTNAAGSGPFTLEKWDPATEAVFTANESYWQGAPNLSKVTLKFTKEASNRVLLLDKGDVDMAIEIPPKDVASLQSNTDLTVASNASNRILFFAMNNKVKPFDNVKVRQAINYAIPYDELLSGVMYGQAKQMKSSVASNTPGFTDAGYVYEHNLDKAKELLTEAGYPDGFTFDFTLGSGFDDWEDDAVLIQAELAKIGVTMNINKLARAQFLEQQKTNNLTSYISKWTSFVNDPGYHLGFLLYGKGSSNYINYSNAEVDKLWDEANLETDAAKRTALYEQAQEIITTEAPWAYLYEYNRIVGMSNKISGYAFYPDEVIRFYPLSITE

Crispr_ID: NZ_CP009285_15

• CRISPR_ID: NZ_CP009285_15
• CRISPR_location: 5450851-5450921
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_15

Consensus_repeat	Method
AGCTGCTGCGGAAGGGGCTACAC	CRISPRCasFinder

spacers of NZ_CP009285_15

>15.1|5450874|25|NZ_CP009285|CRISPRCasFinder
CCTGGGACTGCATCCACTCATGCCA

CRISPR arrays and Neighbor proteins around NZ_CP009285_15

CRISPR arrays

The CRISPR arrays of NZ_CP009285_15

>merge|NZ_CP009285|15|5450851-5450921|CRISPRCasFinder
AGCTGCTGCGGAAGGGGCTACACCCTGGGACTGCATCCACTCATGCCAAGCTGCTGCGGAAGGGGCTACAC

>NZ_CP009285|15|14|5450851-5450921|CRISPRCasFinder
AGCTGCTGCGGAAGGGGCTACAC	CCTGGGACTGCATCCACTCATGCCA
AGCTGCTGCGGAAGGGGCTACAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042215839.1|5452366_5453776_-|replicative-DNA-helicase	unknown	unknown	gnl|CDD|273206
NZ_CP009285.1|WP_157764106.1|5449130_5449292_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215821.1|5445668_5445953_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215827.1|5449293_5449725_-|DUF5348-domain-containing-protein	unknown	unknown	gnl|CDD|379963
NZ_CP009285.1|WP_052429615.1|5453762_5454113_-|hypothetical-protein	unknown	unknown	gnl|CDD|288299
NZ_CP009285.1|WP_042215835.1|5451458_5451872_-|RusA-family-crossover-junction-endodeoxyribonuclease	unknown	unknown	gnl|CDD|377564
NZ_CP009285.1|WP_042215815.1|5444449_5444740_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215829.1|5449741_5450170_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215847.1|5458817_5459078_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215842.1|5455216_5455924_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293819
NZ_CP009285.1|WP_042215840.1|5454072_5454996_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215845.1|5456832_5458821_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|379210
NZ_CP009285.1|WP_042215819.1|5445209_5445449_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_081972151.1|5448783_5448978_-|zinc-finger-domain-containing-protein	unknown	unknown	gnl|CDD|378493
NZ_CP009285.1|WP_042215849.1|5459182_5459413_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215844.1|5455923_5456829_-|recombinase-RecT	unknown	unknown	gnl|CDD|367688
NZ_CP009285.1|WP_157764105.1|5446896_5447007_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215831.1|5450138_5450375_-|IDEAL-domain-containing-protein	unknown	unknown	gnl|CDD|378069
NZ_CP009285.1|WP_042215837.1|5452010_5452193_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_081972402.1|5447099_5448701_-|DNA-cytosine-methyltransferase	unknown	unknown	gnl|CDD|223348

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042215839.1|5452366_5453776_-|replicative-DNA-helicase	gnl|CDD|273206	TIGR00665, DnaB, replicative DNA helicase. This model describes the helicase DnaB, a homohexameric protein required for DNA replication. The homohexamer can form a ring around a single strand of DNA near a replication fork. An intein of > 400 residues is found at a conserved location in DnaB of Synechocystis PCC6803, Rhodothermus marinus (both experimentally confirmed), and Mycobacterium tuberculosis. The intein removes itself by a self-splicing reaction. The seed alignment contains inteins so that the model built from the seed alignment will model a low cost at common intein insertion sites. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP009285.1|WP_042215845.1|5456832_5458821_-|AAA-family-ATPase	gnl|CDD|379210	pfam13476, AAA_23, AAA domain.	1.92656e-07
NZ_CP009285.1|WP_042215842.1|5455216_5455924_-|MBL-fold-metallo-hydrolase	gnl|CDD|293819	cd07733, YycJ-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis YycJ and related proteins; MBL-fold metallo hydrolase domain. Includes the uncharacterized Bacillus subtilis YycJ protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of 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.	3.71298e-24
NZ_CP009285.1|WP_042215827.1|5449293_5449725_-|DUF5348-domain-containing-protein	gnl|CDD|379963	pfam17295, DUF5348, Domain of unknown function (DUF5348).	2.94872e-07
NZ_CP009285.1|WP_052429615.1|5453762_5454113_-|hypothetical-protein	gnl|CDD|288299	pfam11417, Inhibitor_G39P, Loader and inhibitor of phage G40P. G39P inhibits the initiation of DNA replication by blocking G40P replicative helicase. G39P has a bipartite stricture consisting of a folded N-terminal domain and an unfolded C-terminal domain. The C terminal is essential for helicase interaction.	4.19221e-05
NZ_CP009285.1|WP_081972151.1|5448783_5448978_-|zinc-finger-domain-containing-protein	gnl|CDD|378493	pfam10782, zf-C2HCIx2C, Zinc-finger. This bacterial family of proteins is a zinc-finger domain of the C2HC type with an additional cysteine.	0.00301982
NZ_CP009285.1|WP_042215844.1|5455923_5456829_-|recombinase-RecT	gnl|CDD|367688	pfam03837, RecT, RecT family. The DNA single-strand annealing proteins (SSAPs), such as RecT, Red-beta, ERF and Rad52, function in RecA-dependent and RecA-independent DNA recombination pathways. This family includes proteins related to RecT.	3.53354e-39
NZ_CP009285.1|WP_042215831.1|5450138_5450375_-|IDEAL-domain-containing-protein	gnl|CDD|378069	pfam08858, IDEAL, IDEAL domain. This short domain is found at the C-terminus of proteins in the UPF0302 family. The domain is named after the sequence of the most conserved region in some members. The function of this domain is unknown.	8.66712e-10
NZ_CP009285.1|WP_081972402.1|5447099_5448701_-|DNA-cytosine-methyltransferase	gnl|CDD|223348	COG0270, Dcm, Site-specific DNA methylase [DNA replication, recombination, and repair].	2.42284e-06
NZ_CP009285.1|WP_042215835.1|5451458_5451872_-|RusA-family-crossover-junction-endodeoxyribonuclease	gnl|CDD|377564	pfam05866, RusA, Endodeoxyribonuclease RusA. This family consists of several bacterial and phage Holliday junction resolvase (RusA) like proteins. The RusA protein of Escherichia coli is an endonuclease that can resolve Holliday intermediates and correct the defects in genetic recombination and DNA repair associated with inactivation of RuvAB or RuvC.	1.97876e-38

Protein sequences

>NZ_CP009285.1|WP_042215831.1|5450138_5450375_-|IDEAL-domain-containing-protein
MFIDFGMLMQLRYEAMLSVHADAIWQASIQRFNEERLLKLIDQALDDQNPEAFYQYSAELAGVRAVQAYGQVTSASKG
>NZ_CP009285.1|WP_042215829.1|5449741_5450170_-|hypothetical-protein
MGKSHRRPKDESIRKLADRITRAVKAHGITVQRYDAFTTNSVYLKFDYGVANSVRISDHMGKLSRSNRFNLLKNIDHSYVELDRYLKYFYCTNDLEKLVADIIQNRKDQVEKYGPRYYDFLMKRNKAANTDTKGFWSKARIV
>NZ_CP009285.1|WP_042215827.1|5449293_5449725_-|DUF5348-domain-containing-protein
MKDKIKAALIKLEPELKRVAKLIEEGENDGIYDREDPDAQYLRSMFNVISEDLSKTRRYIRQLSAPLVAEETIYKRPDGRYGSRTSYYTSGAAIEYLFTDSWGDQVWVYSHIEHNGEDYYIVNNPKLSLEGLRVRVKRLPMWD
>NZ_CP009285.1|WP_157764106.1|5449130_5449292_-|hypothetical-protein
MNWRAATPQQLRMVMWDPGAHPVHRQEAAAELFRRRRQKWGKTNYKMKRVYPK
>NZ_CP009285.1|WP_081972151.1|5448783_5448978_-|zinc-finger-domain-containing-protein
MMSRLQVVYAISDILQHCGVCPQRVKLSQKYGSTYSKIDGYCNRECPVGGLLQLQGKELIRERA
>NZ_CP009285.1|WP_081972402.1|5447099_5448701_-|DNA-cytosine-methyltransferase
MRSTVEYGGKVYKFKVLCSIDNDPVACRNHDQICGEKTSVVMDLFKRWQYKAWHGHEPPETWRETTPWDIWQAFKEQVPFFLFLSPPCKGLSGLLPSDKAASAQYQALNFLTVHGLEMALQACLEYGGAIPAVIQLENVPRITSRGEPLLKQILKMLKKYGYEVSVRSDHNLGTIGGLGQNRVRFLLKARDPKQIPNVIYYPEAKPMKSIGEVLVPLPAPGDTVAGGPMNKLQQLQWKTWMRLALILAGGDWRDLNKVNWQNLRIAHEPRRGAYEVADWNEPSRAVTSTAGPGRSNGVAAVSDPRLHINSEGKTNILRIQSVDEQSSCITGAAGPYQGGASIADPALKERPSRHPAAYRVVRVDEVAPCVTGTRFGSGAIAIADPLLKCTPRADSYGVQDWDQPAKTVIGSADIHASAAAVTDPRIPKDNEQGVWVIIAQDGTWHRPLTTYELAMLQNFPTHLPDGRPFQLEGCNDAKAREYIGNAVPPGAEEAMGNVILMAAAEAEAGISFQLSWNPVWVAPGEEQRPTVLH
>NZ_CP009285.1|WP_157764105.1|5446896_5447007_+|hypothetical-protein
MEHESFEDKAAALTVQAPAVQAVTASDAVVRMSYVP
>NZ_CP009285.1|WP_042215821.1|5445668_5445953_+|hypothetical-protein
METNYQQVAWNCMNKYVGMTTTDGQSHDGFIAHIDQDYVTLAVPTNEMMNGMPANASTYRQFGYYPGFYPRRRFYPRHIPFGAITALYLLPFFI
>NZ_CP009285.1|WP_042215819.1|5445209_5445449_+|hypothetical-protein
MKKLDLVANKLMGQIVLMADEEKFYPDPNNRMEKYTRPQLLFIRRGILSYENEPYGNKGGWDSTIRELFPALAQWAGIK
>NZ_CP009285.1|WP_042215815.1|5444449_5444740_-|hypothetical-protein
MMKPRYLILKGGSPAIHKLGDIGRDEDDLIFVKSETEDHFIGNFVEGFGFADVEYRKSDCRPLTPGEIEKLNNSAFQLGGVRYKMRVDSEGYPQKN
>NZ_CP009285.1|WP_042215835.1|5451458_5451872_-|RusA-family-crossover-junction-endodeoxyribonuclease
MIQFVVYGEPVAQGRPKFSTAGGFTRAYDPAKSRDYKDYVRLAAREYAPAALLEGALGIAITAYRSTPKSFSKKKAAEAERGEILPVTKPDADNYLKGVKDALKGIIWKDDSQVVDAFVRKRYSNRPRIEVKIKELT
>NZ_CP009285.1|WP_042215837.1|5452010_5452193_-|hypothetical-protein
MSGAWNYWHVYHFMVTYYQNTGLVPERSVLLAEFPSLDPEQVDEGIAEFNLVMGKRGEAG
>NZ_CP009285.1|WP_042215839.1|5452366_5453776_-|replicative-DNA-helicase
MLNREEMLEQMGIQPPIDLEAEQAVLGAALLDQTAYDAAADILQGGEFSDKGHARIFRAMRKLNDAELPIDMVSLTSQLKDSEELEKVGGVSYLARMAGAVPTVANAGYYAERVQEMFLRRQAIDTAMDLLRNAGEEQDVKGFIAMAEHAVSKLSDQSVPIREFATMKDVLMQVWEDAEQRYSVRETSRGITGIRSGFDDLDKMTSGFQRNDLIIVAARPSVGKTAFALNIAQNVAVRAKETVAVFSLEMSNAQLVQRMVCAEGNIDASRMRTGHFEEDDWQKMSMAMGSLSEADIYIDDTPGITVNEIRSKCRRLKKEKDLGMIVIDYLQLIQGRGQRGVNRQEEVSQISRTLKQLARELEVPVIALSQLSRGVEQRQDKRPMMSDLRESGSIEQDADIVAFLYRDDYYDKESEKKNIIEIIISKQRNGPVGTVELVFLKEFNKFVNYERAHSDIPAPPDDIDKRKWA
>NZ_CP009285.1|WP_052429615.1|5453762_5454113_-|hypothetical-protein
MEKLEVILLVRTIKANYPGFDKSPENIERLYKYLKDFPFEAAKENVDAHIKTKEFPPNVAEIRGRLGEQIEREQMKILTDQHFANLDTWSASSKPPPEGYWDEVKRKIRGEANVES
>NZ_CP009285.1|WP_042215840.1|5454072_5454996_-|hypothetical-protein
MTESAREPTMAGLLNQYEAIGGPEEYGPEGIAIMVALWRKSCKLGWKRAFQMTNTELTLQTGIKSRDTINTHRSKLVNAGLIGYTSPPRGSAKGSYTIRFDLIVVGEPVQNSDHFNIVGEEVVQKPDHFSKADGEAVRKLDHFPDTVLKDLSTTITSTTDNEFADEIDQGKPGDMFELLNAFCKMNHRLDIHISPREREAMGRMVAGGTPNPFTIRTMESLLQAKREREGDDFKYPTSFLYYVDGIKKAWLNSQTTAAQTDGVAPRETTDKPQRQTKQQRELAELDMMIEEERRRGEAGGHSSGPHH
>NZ_CP009285.1|WP_042215842.1|5455216_5455924_-|MBL-fold-metallo-hydrolase
MIDIQCLGSSSAGNAYRISDGHTAILLEAGFPYKSIQRALNFRMSDISGCLITHEHLDHSKAAPDIMRAGINIYTSAGTAAARGLSGHRLKVIKALEKFTIGTWTILPFDIQHDVEEPLGFLLANTAGDKLVFLTDTYYCRHRFSGLTHIMCECNYSLDIVNERVAAGHLHPAQKKRLLRSHFSLENVKEMLKVNDTRNVEEIWLLHLSDGNSDAERFKQEIQETTGALVRVADR
>NZ_CP009285.1|WP_042215844.1|5455923_5456829_-|recombinase-RecT
MSTGNQVAIIQKDITDDVNRSLTRLQDDGLILPMNYNASNALKSAFFKLQEVQDKNGKPALEVCSRESVANALLDMVVQGLSPAKTQCYFIVYGSKLQLNRSYFGTQAVLKRLSNVKDIWANVIYKGDVFEYEVAGGREKLVKHETSFENRDNEILGVYAVVKSVDDEEILTVMTKKEVDASWSQSKTSQSVHKKFPQEMAKRTVINRAAKAYINTSDDSDLLVDAINRSTDNEYEERIDVTPEEVKAEIAEHANREVIDIVPEVTPPSSKQQTAPRTKQLVDDPYDFADDVPPLEQEMDF
>NZ_CP009285.1|WP_042215845.1|5456832_5458821_-|AAA-family-ATPase
MSRIELERLGLRNFKGIKEFTLTVNGGYAAVYGDNATGKTTIFDGFTWLFFGKDSQNKADFEIKGLDGAGKVLQHKLEHEVEGVFLIDGRRRTFRRVFSEKWTKKRGSATDAFEGHETNYFLDGVPVKKGEYTAEVDSLIKEELFKLLTSPSYFNEQMKKEDRRKTLLEVCGDLTDAEVIHGNKELAPLPGILSGRDLDSHKKVISSRCAVINKEIKELPVRISEVQRQMPDVTELDEDSLKEDMAVLRNRVVSGEAELSRILSGGEVAVKEKRLREIEGELIAIKSRMQSDVLDKVALKRDAVNQMHMEVNRYRRDIEDKQQRIQINERKAKDRQQEADRLRTEFSELKGLTFEPAGDHDAHCSACGQSLPEDQVKAAHDKAEADFNRRLAERKERINASGKAAVADTQKFEQEIVRFQGEIESLKSALQLLQAELTDADAELTDLRAGVKDPAADPDYASKQAEAATVQQQISDLKASSNDAAAAVRQSILLQRSEIAGMESDLAKFDGVRRAQLRVTELENQERELAAEYERLQHELFLCEEFTKTKVSMLDAKINSKFKLARFRLFEDQINGGIKEVCDTLYKGVPYDGGLNNAARINVGLDIINTLGEHYGFSAPIFVDNAEAVTKLIGTDAQVIRLVVSEADKKLRIETAAIQEAI
>NZ_CP009285.1|WP_042215847.1|5458817_5459078_-|hypothetical-protein
MSTAYSADISGQRIEVEIVPPTNYSPPVLSIRQQFGSFQLHADPEQLAEVEYAIRTYLEGIRYPETPDQQMILHAECESAIEEGIA
>NZ_CP009285.1|WP_042215849.1|5459182_5459413_-|hypothetical-protein
MNIDTGELIRLKQSQPVSGGFVPIPRELQREANKHLSEKDSVIVDLSSNGPLSKWAKAQRKKRRKAVRKSRKQNRK

Crispr_ID: NZ_CP009285_16

• CRISPR_ID: NZ_CP009285_16
• CRISPR_location: 5514189-5514267
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_16

Consensus_repeat	Method
CAATGTATTCGGTTTTTCTCATACATT	CRISPRCasFinder

spacers of NZ_CP009285_16

>16.1|5514216|25|NZ_CP009285|CRISPRCasFinder
TGGCCCATCTATCCTATCGTCGGGG

CRISPR arrays and Neighbor proteins around NZ_CP009285_16

CRISPR arrays

The CRISPR arrays of NZ_CP009285_16

>merge|NZ_CP009285|16|5514189-5514267|CRISPRCasFinder
CAATGTATTCGGTTTTTCTCATACATTTGGCCCATCTATCCTATCGTCGGGGCAATGTATTCGGTTTTTCGCATACATT

>NZ_CP009285|16|15|5514189-5514267|CRISPRCasFinder
CAATGTATTCGGTTTTTCTCATACATT	TGGCCCATCTATCCTATCGTCGGGG
CAATGTATTCGGTTTTTCGCATACATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_020426549.1|5510551_5510755_-|stage-III-sporulation-protein-AC	unknown	unknown	gnl|CDD|131895
NZ_CP009285.1|WP_042138739.1|5512967_5513834_+|YitT-family-protein	unknown	unknown	gnl|CDD|224203
NZ_CP009285.1|WP_042215962.1|5515915_5516473_-|elongation-factor-P	unknown	unknown	gnl|CDD|234788
NZ_CP009285.1|WP_042215957.1|5511279_5512281_-|stage-III-sporulation-protein-AA	unknown	unknown	gnl|CDD|274324
NZ_CP009285.1|WP_042215950.1|5507289_5507928_-|stage-III-sporulation-protein-AG	unknown	unknown	gnl|CDD|274319
NZ_CP009285.1|WP_042215964.1|5516518_5517589_-|aminopeptidase-P-family-protein	unknown	unknown	gnl|CDD|223085
NZ_CP009285.1|WP_042215975.1|5522646_5523072_-|transcriptional-regulator-MntR	unknown	unknown	gnl|CDD|179669
NZ_CP009285.1|WP_042219837.1|5508845_5510105_-|stage-III-sporulation-protein-AE	unknown	unknown	gnl|CDD|213743
NZ_CP009285.1|WP_042215968.1|5518312_5519317_+|DUF1385-domain-containing-protein	unknown	unknown	gnl|CDD|226390
NZ_CP009285.1|WP_042215977.1|5523264_5524341_+|spore-photoproduct-lyase	unknown	unknown	gnl|CDD|213890
NZ_CP009285.1|WP_042215970.1|5519324_5519663_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042215960.1|5514411_5515665_-|aspartate-kinase	unknown	unknown	gnl|CDD|235843
NZ_CP009285.1|WP_042215952.1|5510152_5510542_-|stage-III-sporulation-protein-AD	unknown	unknown	gnl|CDD|131896
NZ_CP009285.1|WP_039295545.1|5512363_5512606_-|YqhV-family-protein	unknown	unknown	gnl|CDD|378514
NZ_CP009285.1|WP_042215973.1|5520795_5522472_-|family-10-glycosylhydrolase	unknown	unknown	gnl|CDD|224563
NZ_CP009285.1|WP_042215955.1|5510768_5511287_-|stage-III-sporulation-protein-AB	unknown	unknown	gnl|CDD|181372
NZ_CP009285.1|WP_042215948.1|5506143_5507043_-|SpoIIIAH-like-family-protein	unknown	unknown	gnl|CDD|378918
NZ_CP009285.1|WP_042215971.1|5519746_5520727_-|patatin-like-phospholipase-family-protein	unknown	unknown	gnl|CDD|132846
NZ_CP009285.1|WP_052429617.1|5507981_5508779_-|stage-III-sporulation-protein-AF	unknown	unknown	gnl|CDD|378212
NZ_CP009285.1|WP_042215966.1|5517664_5518156_-|hypothetical-protein	unknown	unknown	gnl|CDD|314111

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_020426549.1|5510551_5510755_-|stage-III-sporulation-protein-AC	gnl|CDD|131895	TIGR02848, Stage_III_sporulation_protein_AC, stage III sporulation protein AC. Members of this protein family are designated SpoIIIAC, part of the spoIIIA operon of sporulation genes whose mutant phenotype is linked to sporulation stage III. Members of this family are encoded by the genome of a species if and only if that species is capable of endospore formation, as in Bacillus subtilis. The molecular function of this small, probable integral membrane protein is unknown. [Cellular processes, Sporulation and germination].	2.33834e-15
NZ_CP009285.1|WP_042138739.1|5512967_5513834_+|YitT-family-protein	gnl|CDD|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	5.2947e-64
NZ_CP009285.1|WP_042215962.1|5515915_5516473_-|elongation-factor-P	gnl|CDD|234788	PRK00529, PRK00529, elongation factor P; Validated.	2.60443e-108
NZ_CP009285.1|WP_042215957.1|5511279_5512281_-|stage-III-sporulation-protein-AA	gnl|CDD|274324	TIGR02858, Stage_III_sporulation_protein_AA, stage III sporulation protein AA. Members of this protein are the stage III sporulation protein AA, encoded by one of several genes in the spoIIIA locus. It seems that this protein is found in a species if and only if that species is capable of endospore formation. [Cellular processes, Sporulation and germination].	2.67037e-122
NZ_CP009285.1|WP_042215950.1|5507289_5507928_-|stage-III-sporulation-protein-AG	gnl|CDD|274319	TIGR02830, Stage_III_sporulation_protein_AG, stage III sporulation protein AG. CC A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, a member of this panel, is found in a spore formation operon and is designated stage III sporulation protein AG. [Cellular processes, Sporulation and germination].	5.7836e-49
NZ_CP009285.1|WP_042215964.1|5516518_5517589_-|aminopeptidase-P-family-protein	gnl|CDD|223085	COG0006, PepP, Xaa-Pro aminopeptidase [Amino acid transport and metabolism].	1.51134e-121
NZ_CP009285.1|WP_042215975.1|5522646_5523072_-|transcriptional-regulator-MntR	gnl|CDD|179669	PRK03902, PRK03902, transcriptional regulator MntR.	1.6734e-81
NZ_CP009285.1|WP_042219837.1|5508845_5510105_-|stage-III-sporulation-protein-AE	gnl|CDD|213743	TIGR02829, Stage_III_sporulation_protein_AE, stage III sporulation protein AE. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, a member of this panel, is found in a spore formation operon and is designated stage III sporulation protein AE. [Cellular processes, Sporulation and germination].	7.71792e-123
NZ_CP009285.1|WP_042215968.1|5518312_5519317_+|DUF1385-domain-containing-protein	gnl|CDD|226390	COG3872, COG3872, Predicted metal-dependent enzyme [General function prediction only].	1.78074e-133
NZ_CP009285.1|WP_042215977.1|5523264_5524341_+|spore-photoproduct-lyase	gnl|CDD|213890	TIGR04070, photo_TT_lyase, spore photoproduct lyase. DNA damage to bacterial spores from ultraviolet light accumulates in the form of 5-thyminyl-5,6-dihydrothymine, spore photoproduct. The damage is repaired by spore photoproduct lyase, a member of the radical SAM family of enzymes. The score of this model is set to restrict itself to spore-forming members of the Firmicutes, but additional homologs scoring below the trusted cutoff tend to occur in radioresistant organisms (e.g. Kineococcus radiotolerans) and may be functionally equivalent. A related family in the Mycobacterium lineage is described by family TIGR03886, and may or may not be equivalent in function. [DNA metabolism, DNA replication, recombination, and repair, Cellular processes, Sporulation and germination].	0
NZ_CP009285.1|WP_042215960.1|5514411_5515665_-|aspartate-kinase	gnl|CDD|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	0
NZ_CP009285.1|WP_042215952.1|5510152_5510542_-|stage-III-sporulation-protein-AD	gnl|CDD|131896	TIGR02849, Stage_III_sporulation_protein_AD, stage III sporulation protein AD. Members of this family are the uncharacterized protein SpoIIIAD, part of the spoIIIA operon that acts at sporulation stage III as part of a cascade of events leading to endospore formation. Note that the start sites of members of this family as annotated tend to be variable; quite a few members have apparent homologous protein-coding regions continuing upstream of the first available start codon. The length of the alignment and the scoring cutoff thresholds for the model have been set to try to detect all valid members of the family, even if annotation of the start site begins too far downstream. [Cellular processes, Sporulation and germination].	1.15303e-24
NZ_CP009285.1|WP_039295545.1|5512363_5512606_-|YqhV-family-protein	gnl|CDD|378514	pfam10942, DUF2619, Protein of unknown function (DUF2619). This bacterial family of proteins has no known function.	2.69491e-23
NZ_CP009285.1|WP_042215973.1|5520795_5522472_-|family-10-glycosylhydrolase	gnl|CDD|224563	COG1649, COG1649, Uncharacterized protein conserved in bacteria [Function unknown].	1.44582e-89
NZ_CP009285.1|WP_042215955.1|5510768_5511287_-|stage-III-sporulation-protein-AB	gnl|CDD|181372	PRK08307, PRK08307, stage III sporulation protein SpoAB; Provisional.	6.28005e-59
NZ_CP009285.1|WP_042215948.1|5506143_5507043_-|SpoIIIAH-like-family-protein	gnl|CDD|378918	pfam12685, SpoIIIAH, SpoIIIAH-like protein. Stage III sporulation protein AH (SpoIIIAH) is a protein that is involved in forespore engulfment. It forms a channel with SpoIIIAH that is open on the forespore end and closed (or gated) on the mother cell end. This allows sigma-E-directed gene expression in the mother-cell compartment of the sporangium to trigger the activation of sigma-G forespore-specific gene expression by a pathway of intercellular signaling. This family of proteins is found in bacteria, archaea and eukaryotes and so must have a wider function that in sporulation. Proteins in this family are typically between 174 and 223 amino acids in length.	5.71814e-19
NZ_CP009285.1|WP_042215971.1|5519746_5520727_-|patatin-like-phospholipase-family-protein	gnl|CDD|132846	cd07207, Pat_ExoU_VipD_like, ExoU and VipD-like proteins; homologus to patatin, cPLA2, and iPLA2. ExoU, a 74-kDa enzyme, is a potent virulence factor of Pseudomonas aeruginosa. One of the pathogenic mechanisms of P. aeruginosa is to induce cytotoxicity by the injection of effector proteins (e.g. ExoU) using the type III secretion (T3S) system. ExoU is homologus to patatin and also has the conserved catalytic residues of mammalian calcium-independent (iPLA2) and cytosolic (cPLA2) PLA2. In vitro, ExoU cytotoxity is blocked by the inhibitor of cytosolic and Ca2-independent phospholipase A2 (cPLA2 and iPLA2) enzymes, suggesting that phospholipase A2 inhibitors may represent a novel mode of treatment for acute P. aeruginosa infections. ExoU requires eukaryotic superoxide dismutase as a cofactor and cleaves phosphatidylcholine and phosphatidylethanolamine in vitro. VipD, a 69-kDa cytosolic protein, belongs to the members of Legionella pneumophila family and is homologus to ExoU from Pseudomonas. Even though VipD shows high sequence similarity with several functional regions of ExoU (e.g. oxyanion hole, active site serine, active site aspartate), it has been shown to have no phospholipase activity. This family includes ExoU from Pseudomonas aeruginosa and VipD of Legionella pneumophila.	1.81403e-58
NZ_CP009285.1|WP_052429617.1|5507981_5508779_-|stage-III-sporulation-protein-AF	gnl|CDD|378212	pfam09581, Spore_III_AF, Stage III sporulation protein AF (Spore_III_AF). This family represents the stage III sporulation protein AF (Spore_III_AF) of the bacterial endospore formation program, which exists in some but not all members of the Firmicutes (formerly called low-GC Gram-positives). The C-terminal region of these proteins is poorly conserved.	9.34385e-31
NZ_CP009285.1|WP_042215966.1|5517664_5518156_-|hypothetical-protein	gnl|CDD|314111	pfam11085, YqhR, Conserved membrane protein YqhR. This family is conserved in the Bacillaceae family of the Firmicutes. The function is not known.	2.21227e-25

Protein sequences

>NZ_CP009285.1|WP_042138739.1|5512967_5513834_+|YitT-family-protein
MQVRNFVVPLVSGTVARQVKEVAIIIFSAFLVAGGLRLFLIPHQLLSGGVAGTASIIGYLTNPKYISLYYFAINLPILIWGFVAVGKKYICYSMLSVISTTWFLNIIPVVKLTKDPILASIFGGVIIAGGVGFSLRAGGSSGGFDILGSIITRKRDIPMGTVLFVMDGLVILSLGFFKSWDSALYAMLCIFVKSRVVDMIHIRHVKLTCFIVTKEREKMLNRLTCLPHGVTVVNAEGGYSHEGNTMLMTVTTRYELADLRKTILETDPKSFVNVLETVEIMGRFRRLS
>NZ_CP009285.1|WP_039295545.1|5512363_5512606_-|YqhV-family-protein
MAGLRLLSGSVEIAAALIMLRLNQVDKALAVNSGLALVGPTILILTTAVGLTGMAQQLSWGKLGWIGCGVAFLLIGILKK
>NZ_CP009285.1|WP_042215957.1|5511279_5512281_-|stage-III-sporulation-protein-AA
MANDWLLLFPEKVRALLGGLPAALLDKVEEVRVREGRPLEINYSGKYHFVGVNCSLTQLPGEAYKPDREDTHRLLDLISNHSLYTMEEELRKGFITIPGGHRIGLSGRTVLSGGGVEHLRDITGFNVRIAREVHGLADGVLPYLLDRGRQRIMHTLILSPPQHGKTTLLRDLARQISAGGQGGREGSRPGLKVGIVDERSEIAGSRRGIPAFDVGPRTDILDGCPKAEGMMMMIRSLSPDVLIADEIGRLEDADAVTEALHAGISVVASAHGKEVSELARRPGLGGLLEHRMFERYVILHRSESGLSFRILDAQKRGLLLISPEERIGGDRHA
>NZ_CP009285.1|WP_042215955.1|5510768_5511287_-|stage-III-sporulation-protein-AB
MLKLLGAVLIVLAGTLAGFKRAAQYADRPRHIRGLIAALQRLETEIQYGYTPLPEALRRIGMQSKDPLRAFFLTAAEEMSPPHNCSAEEAVRRSMEIHWNSASLKGTEKEIFRQLSCTLGTSDRSNQSTHIALALQQLKQEETAAREDQGKYEKVSKSLGLLLGALIVILIF
>NZ_CP009285.1|WP_020426549.1|5510551_5510755_-|stage-III-sporulation-protein-AC
MNIEVNAIFQIAGIGIIIAMIHTVLKQMGKEDIAHWVTIVGFIIVLFMVIRMLDGLLQEIKTIFLFQ
>NZ_CP009285.1|WP_042215952.1|5510152_5510542_-|stage-III-sporulation-protein-AD
MEIIQVVGIGILSTVLILVLKEQKPMFAFLLATATGILIFLFLIGKIGTILGTLERVAESSGMEMIYIKTVFKIIGISYIAEFGAQIVRDAGQESIASKIELAGKVLIMVLAVPIISIIIETVMKLLPA
>NZ_CP009285.1|WP_042219837.1|5508845_5510105_-|stage-III-sporulation-protein-AE
MQERSVFRPPKLYKLLVLLPCLLLLLCAGTTYAAPAPPTQAQAQSGGSTGGGSPSAVDQWVKGQVENLPTDGVQTYWDQLMKDYGGFFPDGKTPSLMDMLLPGDNGLSFKSVLSGLTRFMWHEVLYNGKLLVTIVMISVLSMILETLQTAFERKSVSKIAYMLCYMVVLVIAVNSFNIAIGYAKDAIDRMIDFMMAMIPLLFALLASMGNIVTVSVTHPLIVFMIHTVGTMIHTIVFPLLFFSAVLHLVSAMSEKYKLTQLANLLRNIGAGLLGVLLTVFLGVISVRGITSSVTDGVTIRAAKYITGNFVPVIGKMFADATDTVISASLLVKNAIGLSGVIIILFLCAFPAIKILVLALIYNVAAAVMQPLGETPIVVCLQTIGKSMIYVFAALAAVSLMFFLAVTIMLTAGNVTVMMR
>NZ_CP009285.1|WP_052429617.1|5507981_5508779_-|stage-III-sporulation-protein-AF
MSWLSGWLHELILVVLMAAFVEMLLPSKSMERYARLVLSLLVLLTMLNPIVSMLKGDASKELSLAMEQQERNGGLLSGAGDGADSLEKILADGRMLAEGARDQSLKLAAEEIAGQMRDQIAGSTGIRGVNVTVKLGMGPNPSAPLGEDVPLISSVTVDLPAAGAVAASGSPGSGTGSPPAANPASGPIRITPVEPVQVSLDNDGAASEGSDASAGVSPSSAAGNGAQEAPADAEAESIIKLLEQNWNLDPDLINVLSGGANAVKS
>NZ_CP009285.1|WP_042215950.1|5507289_5507928_-|stage-III-sporulation-protein-AG
MGKWLKKLEQWAGGGSGSPKRSHTFRWLIIIGLLGVAIMLFNSFVNVKKLDNENTGREPPASETSQAVLQQEAVTTNSFDSIELAMENRTKEILEKIVGVGTVDIMVTVDSTEEIVVQRNMNDSQQQSEETDASGGKRHTTQYTRDGEIVTYSQSGDETPIITKRIKPQVRGVLVVAKGAENKVVRSLIEQAVEKGLNVPSYRISVVPRKQE
>NZ_CP009285.1|WP_042215948.1|5506143_5507043_-|SpoIIIAH-like-family-protein
MKGKRQTIWLVSMLSLMVVLSAYYLFTEDTGASIPKETAGSIQVDTVKDGTGGGTATTLDSGLVINEVSTDGSVVADAGTLTDDSNTAAVTEDSSKAAADEAAAAAVTDDSTAAVADNGSADTGDAAKDTAAADTAGKTDKAATAAADQGKDTKDTVAASDKTPAKDDAAILDEVASQSVSASSLFTNYLYEREQQNLKDHNDLLALINDMDKTPAENAVAQEQLSKLEEKESKITGIEEQLQQKYGEAIVKEEAGDAYTIVVLSDKLDVKQAVGIVDLVMKELSVSQDKIKVQYVSEQ
>NZ_CP009285.1|WP_042215960.1|5514411_5515665_-|aspartate-kinase
MSLYVMKFGGSSVGDIERMKRVAKRIADKQDEGHRCVVVVSAMGDTTDELIDQAKQLNGQPPAREMDMLMTTGEQISVALLSIALHGIGRNAVSYTGWQAGFRTDETHGRARISEIVPRRVLESLEREQIVIVAGFQGMTLDGEITTLGRGGSDTTAVALAAAIKADVCEIYTDVDGIYSTDPRIVKTARKLKEISYDEMLELANLGAAVLHPRAVEYAKRYQVKLVVRSSFNHNEGTVVKEEASMEQGVVVSGIAYDKNVARISILGVPDVPGVLAQVFGKLAEEGVDVDIIVQSGVQNQTADFSFTVALSDLEKAKQVIEGLHSVLPYREVTSEDNLVKVSIVGAGMVSHPGVAAQMFEVISNEGVSIKMVSTSEIKVSCVIESGNLQQIIQALHTAYNLDTTEQAFVGGPQDRR
>NZ_CP009285.1|WP_042215962.1|5515915_5516473_-|elongation-factor-P
MISVNDFKTGLTVEVEGDIFTVLDFQHVKPGKGAAFVRSKLKNLRNGNTVERTFRAGETIGRAIIENRGVQYLYASGSEHVFMDNETYDQFELTAKQLEWELNFLRENMTVNIVSYQGEILGINLPTSVELKVTETEPGVKGNTAQGATKAATLETGHTVQVPLFINEGDVLLIDTREGKYISRA
>NZ_CP009285.1|WP_042215964.1|5516518_5517589_-|aminopeptidase-P-family-protein
MGNKRVSKLRKVLQEQGLDAMLITSGYNRRYLSGFTGSSGYVLVTGDDSYLLTDFRYMTQASEQVTGLKIVQHAAKFIDTVRELLPQGGQVRIGFEQDDVTFSAYTAYAAALQPAVMVPVSKAVENLRMFKDEEELAIMQRACDLADATYSHILNVIKPGMTERDVDLEMEFYMRTHGATSSSFDTIVASGERSAMPHGVASSKIIQNNEFVTFDFGALLDGYCSDVTRTIALGSPDPKLKEIYDIVLEAQLHTLAHIKPGMTGRECDALARDIITRYGYGEYFGHSTGHGLGMEVHEFPRLSKLADEIMEPGMVVTVEPGIYLSGLGGVRIEDDIVITESGITLLTHSSKDYTVL
>NZ_CP009285.1|WP_042215966.1|5517664_5518156_-|hypothetical-protein
MSSSNKQKSVHTNPFYFAIELGFFAGLIWGGARWLMYVLHFTKVIPGFLAEPFFKHEFLMTPAGHLLGYLSFIVFSVIVSLIYVLIFRRLKGPWPGMIYGVLWWSAVFLAGSWQFLMQPPFRLPWNSVISEFCLFLLWGLFIGYTAAIEYTDERKREQQTKLA
>NZ_CP009285.1|WP_042215968.1|5518312_5519317_+|DUF1385-domain-containing-protein
MSQETPSYGGQAVIEGVMFGGKHINVTAVRRKNQEITFLEVPKSDKSWVLKLRKIPLLRGIVSIIDSSAKGSKHLNYSAESYAEDETEPEELAKQKEKDKDKKKDEGWSLGMIFGVAVMGILSFLFGKIIFTLVPVFVEDFLFKNAFDNYILHNLVEGAIKLTLLLVYLFAISQTPVIKRLFQYHGAEHKVISAFEAGEELTVANVQKYSRLHYRCGSSFMMLTIILGVIIYSVVPWDNLMERVLQRIILLPVVIGISFEVLKGTNAVRDIPGLKYLGYPGLWLQLLTTKEPKDDMVEVSIASFNRMRELDAAIEARGYSEASVSGGILDPAKG
>NZ_CP009285.1|WP_042215970.1|5519324_5519663_+|hypothetical-protein
MIRHALIFWISIALAALGLVTQFMARGLSALSIFILPALLLALLYYAYKVLPGRVAGGSGRSRTKVKPSAKTMSKVAGIRKTQASPGKRKTYPFQVIEGSKGKNDDQLPKYH
>NZ_CP009285.1|WP_042215971.1|5519746_5520727_-|patatin-like-phospholipase-family-protein
MEINAVFEGGGVKGIALAGAVEATERAGRTFRRVAGTSSGSIIASLLAAGYNGEAMSRIIRETPFTSFLKRGALYNTAVVGPAIRVLIKKGLYSGQALESWIRGILLEKGVVTFSDLPRGRLTVIASDITNGRIVVLPDDLELYGISPDSFEVAKAVRMSCSIPYFFDPVMLRLNGEAARRKSFAEQFVYMVDGGMLSNFPLWLFDEKKDGFQSPERRTPTVGYQLIGKTQPQPHRITGPFSMLQAMVGTMLSAHDERYIETDKFVRTVKIPTLGISTTQFHISPEQSDAIYAAGLAAGADFFKNWRPPHSTRPYIHPNQLTGPKL
>NZ_CP009285.1|WP_042215973.1|5520795_5522472_-|family-10-glycosylhydrolase
MNYRKWIVGLLVVMLCLPVWTTAARAASVQISIELDGESLSTDVPPYITRTNVTMVPVGVVSKGLGAGVVWDQASKTATISKGNTVLKLTSGSKSAIVNDASVSLDTSVQITQGRVMVPLRFVSEQLGLQVVWNQATKHIALYSNIEIGGPSTPSTPSVPAVSTPSVPTPVVPTPTVPTPTVPSIPGAKTGKAMKGAWVSTVFNLDWPSTASAGNADKQKKEFDSMLDKLQAAGFNSVFVQVRPSGDALYPSQIVPWSKVLSGTQGKEPGYDPLQYMVSSAHSRGMQFHAWFNPFRATTDDKTTGLAANHVAKLHPEWIVKADSKLYINPGIPEARQHIIDTVMEVVRGYDIDGVHLDDYFYPSNVTFADDTAFKTYNSQAIATKGDWRRDNINQFIRQLGAEIHAVKPAVSFGVSPFGVWRNKKADSTGSDTTAGVSAYDDMYADVRTWIKSGWVDYVAPQVYWSLSFSAARYDKLVDWWVNEVAGTGVKLYIGLASYKVGDTKQTAEWQSGDQIINQLKYNEKYDEVSGSILFRANDIVVRDPFGLASLLSFYFKS
>NZ_CP009285.1|WP_042215975.1|5522646_5523072_-|transcriptional-regulator-MntR
MPTPSMEDYLERIYKLIDEKGYARVSDIAEGLEVHPSSVTKMIQKLDKDEYLIYEKYRGLVLTSKGKKVGKRLVDRHQLLEEFLGIIGVQQEHIYKDVEGIEHHLSWDSITRIETLVEYFRRDEARLQTLYDIHHEMASDS
>NZ_CP009285.1|WP_042215977.1|5523264_5524341_+|spore-photoproduct-lyase
MNVVTPERPPAKRTRKPTGLFIPELVFFEPDALNYPKGERIMEWVKARNIPFRMTTSHNRITNLPGETEVEQYKIAKRTLVVGLRKTLTFDQSKPSADYAIPIATGCMGHCHYCYLQTTLGSKPYIRVYVNTGDIIDAAKKYISERAPEITTFEAACTSDPLGLEHITGSLTELIEFMAEEPLGRLRFVTKYQHVEPLLGLKHNGHTRVRFSVNADYVIKNFEPATSRFEERIEAAGQIARAGYPLGFIIAPIIWHDGWEEGYAELLEKLARTLPPGIGKGLTFEMIQHRFTKTAKTVIEKRYPKSKLEMDIEKRKKKWGKWGQNKYVYPDEQQTALREFITERIFEHFPEAAIDYFT

Crispr_ID: NZ_CP009285_17

• CRISPR_ID: NZ_CP009285_17
• CRISPR_location: 5780240-5780420
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP009285_17

Consensus_repeat	Method
GTTGTATTTCATACAACAATTCTCC	CRISPRCasFinder

spacers of NZ_CP009285_17

>17.1|5780265|27|NZ_CP009285|CRISPRCasFinder
TCATTCAAGCCGTTTAATGGAACAATT
>17.2|5780317|27|NZ_CP009285|CRISPRCasFinder
TGCACATCCCGATATAACAGTACCTAA
>17.3|5780369|27|NZ_CP009285|CRISPRCasFinder
CGCACATCCCGATATATCTGCATCCGA

CRISPR arrays and Neighbor proteins around NZ_CP009285_17

CRISPR arrays

The CRISPR arrays of NZ_CP009285_17

>merge|NZ_CP009285|17|5780240-5780420|CRISPRCasFinder
GTTGTACAAAAGGCAACATTTCTCCTCATTCAAGCCGTTTAATGGAACAATTGTTGTATTTCATACAACAATTCTCCTGCACATCCCGATATAACAGTACCTAAGTTGTATTTCATACAACAATCCTCCCGCACATCCCGATATATCTGCATCCGAATTGTATTTCATACAACACTTTACC

>NZ_CP009285|17|16|5780240-5780420|CRISPRCasFinder
GTTGTACAAAAGGCAACATTTCTCC	TCATTCAAGCCGTTTAATGGAACAATT
GTTGTATTTCATACAACAATTCTCC	TGCACATCCCGATATAACAGTACCTAA
GTTGTATTTCATACAACAATCCTCC	CGCACATCCCGATATATCTGCATCCGA
ATTGTATTTCATACAACACTTTACC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042216281.1|5769093_5770692_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_042216309.1|5799089_5799935_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042216305.1|5795364_5797155_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009285.1|WP_042216287.1|5774424_5775300_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|212492
NZ_CP009285.1|WP_081970085.1|5791809_5792649_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042216293.1|5778762_5779899_-|glycoside-hydrolase-family-88-protein	unknown	unknown	gnl|CDD|369381
NZ_CP009285.1|WP_042216285.1|5773805_5774258_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP009285.1|WP_167549569.1|5779976_5780207_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042216307.1|5797267_5798899_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_052429629.1|5765608_5766955_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_CP009285.1|WP_042216289.1|5775329_5776796_+|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_CP009285.1|WP_042216291.1|5776857_5778753_-|DUF2264-domain-containing-protein	unknown	unknown	gnl|CDD|378358
NZ_CP009285.1|WP_042216303.1|5793758_5795102_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP009285.1|WP_052429630.1|5783814_5784651_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_CP009285.1|WP_042216301.1|5792664_5793603_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_081972169.1|5784977_5791652_-|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|366896
NZ_CP009285.1|WP_042216297.1|5780562_5782374_-|heparinase-II/III-family-protein	unknown	unknown	gnl|CDD|377945
NZ_CP009285.1|WP_167549568.1|5767143_5768946_+|histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009285.1|WP_042216299.1|5782450_5783593_-|DUF2264-domain-containing-protein	unknown	unknown	gnl|CDD|378358
NZ_CP009285.1|WP_042216282.1|5770837_5773681_-|glycosyl-hydrolase-115-family-protein	unknown	unknown	gnl|CDD|379757

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042216281.1|5769093_5770692_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.46446e-56
NZ_CP009285.1|WP_042216309.1|5799089_5799935_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.30937e-75
NZ_CP009285.1|WP_042216305.1|5795364_5797155_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	5.91681e-47
NZ_CP009285.1|WP_042216287.1|5774424_5775300_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|212492	cd05327, retinol-DH_like_SDR_c_like, retinol dehydrogenase (retinol-DH), Light dependent Protochlorophyllide (Pchlide) OxidoReductase (LPOR) and related proteins, classical (c) SDRs. Classical SDR subgroup containing retinol-DHs, LPORs, and related proteins. Retinol is processed by a medium chain alcohol dehydrogenase followed by retinol-DHs. Pchlide reductases act in chlorophyll biosynthesis. There are distinct enzymes that catalyze Pchlide reduction in light or dark conditions. Light-dependent reduction is via an NADP-dependent SDR, LPOR. Proteins in this subfamily share the glycine-rich NAD-binding motif of the classical SDRs, have a partial match to the canonical active site tetrad, but lack the typical active site Ser. This subgroup includes the human proteins: retinol dehydrogenase -12, -13 ,and -14, dehydrogenase/reductase SDR family member (DHRS)-12 , -13 and -X (a DHRS on chromosome X), and WWOX (WW domain-containing oxidoreductase), as well as a Neurospora crassa SDR encoded by the blue light inducible bli-4 gene. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.32133e-55
NZ_CP009285.1|WP_042216293.1|5778762_5779899_-|glycoside-hydrolase-family-88-protein	gnl|CDD|369381	pfam07470, Glyco_hydro_88, Glycosyl Hydrolase Family 88. Unsaturated glucuronyl hydrolase catalyzes the hydrolytic release of unsaturated glucuronic acids from oligosaccharides (EC:3.2.1.-) produced by the reactions of polysaccharide lyases.	8.02811e-12
NZ_CP009285.1|WP_042216285.1|5773805_5774258_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	4.96574e-18
NZ_CP009285.1|WP_081970085.1|5791809_5792649_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.60757e-86
NZ_CP009285.1|WP_042216307.1|5797267_5798899_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	8.52539e-38
NZ_CP009285.1|WP_052429629.1|5765608_5766955_-|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.69633e-55
NZ_CP009285.1|WP_042216289.1|5775329_5776796_+|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.02044e-110
NZ_CP009285.1|WP_042216291.1|5776857_5778753_-|DUF2264-domain-containing-protein	gnl|CDD|378358	pfam10022, DUF2264, Uncharacterized protein conserved in bacteria (DUF2264). Members of this family of hypothetical bacterial proteins have no known function.	3.07319e-168
NZ_CP009285.1|WP_042216303.1|5793758_5795102_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.95719e-57
NZ_CP009285.1|WP_052429630.1|5783814_5784651_+|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.56892e-20
NZ_CP009285.1|WP_042216301.1|5792664_5793603_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.84218e-94
NZ_CP009285.1|WP_081972169.1|5784977_5791652_-|S-layer-homology-domain-containing-protein	gnl|CDD|366896	pfam02057, Glyco_hydro_59, Glycosyl hydrolase family 59.	1.89551e-98
NZ_CP009285.1|WP_042216297.1|5780562_5782374_-|heparinase-II/III-family-protein	gnl|CDD|377945	pfam07940, Hepar_II_III, Heparinase II/III-like protein. This family features sequences that are similar to a region of the Flavobacterium heparinum proteins heparinase II and heparinase III. The former is known to degrade heparin and heparin sulphate, whereas the latter predominantly degrades heparin sulphate. Both are secreted into the periplasmic space upon induction with heparin.	5.41824e-06
NZ_CP009285.1|WP_167549568.1|5767143_5768946_+|histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.20819e-60
NZ_CP009285.1|WP_042216299.1|5782450_5783593_-|DUF2264-domain-containing-protein	gnl|CDD|378358	pfam10022, DUF2264, Uncharacterized protein conserved in bacteria (DUF2264). Members of this family of hypothetical bacterial proteins have no known function.	9.9593e-138
NZ_CP009285.1|WP_042216282.1|5770837_5773681_-|glycosyl-hydrolase-115-family-protein	gnl|CDD|379757	pfam15979, Glyco_hydro_115, Glycosyl hydrolase family 115. Glyco_hydro_115 is a family of glycoside hydrolases likely to have the activity of xylan a-1,2-glucuronidase, EC:3.2.1.131, or a-(4-O-methyl)-glucuronidase EC:3.2.1.-.	1.41456e-169

Protein sequences

>NZ_CP009285.1|WP_167549569.1|5779976_5780207_-|hypothetical-protein
MLYFMQDFTMVGEPGTSAAIAAPGKPLGSCCARRPEAAAHAARKAATHAARKLRRPPPGSSGARRRKPPELPDLAW
>NZ_CP009285.1|WP_042216293.1|5778762_5779899_-|glycoside-hydrolase-family-88-protein
MSGTIQQAWVDEAWSKALEKTLANSLRIGAEFPHASQGGKYVLETPSWWTAGFWPGMLWQLYAVSGDESLKDIAERCEQRLDEVLDGYVKLDHDLGFMWLLTSVANYKLTGTEESRVRALKAANYLAARFNLKGRYIRAWNPWREGEDNSGVAIIDCSMNTSLLFWASEVTGDPRYRHIAEAHMDTVLEHFIRPDGSVYHIVNFNPETGEVVEKRGGQGYAPESAWSRGAAWALYGLSLAYHHTGKQSYLNASKQVAHFFLTRLPEDQVPHWDFRAPGEIGEIRDSSAGSCAASGLLLLASQVDEAEAHVYRNGALRITESLYRNYGTWDNAEEEGLLLHGTSNYPENRNIDVPLIYGDFFYVEALARIKEAGPFYWE
>NZ_CP009285.1|WP_042216291.1|5776857_5778753_-|DUF2264-domain-containing-protein
MTNGKAASEILSSRIADNPLRTREDLVTALEQLTGPLRPLYSKGGARLEIGRSGASYPAATAGMEGFSRVLWGLIPLLIGGGNSGILDIVLNGIRHGTDPAHDEYWGDVRDYDQRLVEMAAFGFALAAVPEQIWSPLAPQEQDHLYNWLNQINSHPCYDCNWLFFNVLVNVGFRTIGRPYDAVQLENNLQRMDAFYLGEGWYSDGVDGHSDYYGPFAIHYYSLLYAKLMEQEDPERSRLFKERARLFAAEFLGWFAPDGSALPYGRSLAYRFAQSAFWSALAYADVEGFPAGVVKGIVLRNLRWWFSQPIFDAAGVLTIGYTYPNLVMAENYNAPGSPYWALKTFLPLALGAEHPFWSEEELPLPEIPAVMVQKPAHLVLVRTPASGHVAAFNSGHLYTNEHTHTSAKYEKFVYSTGFGFSVPRSEWGLSQGAFDSMLALSEGGDNLYRVRRRNLESEITDNVLRSVWKPWANVEVRTWVVAGLPWHIRIHRIETGRALDAAEGGFALGQETELAQQTDNSGIAVSTAWGTSGIKGLMGYGKAELIWPNANTNVLRPRTVLPTLTATLEPGIHWLASAVYGDPSADSSARQVNGVGNILEQSPESLLQVTFAEDGIMVQTTGGTEIMISLL
>NZ_CP009285.1|WP_042216289.1|5775329_5776796_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MSQDIQLNSIKKGPLLFIMILGAFIAVLNQTIMSVAIPELITDFNIAATTAQWLTTGYMLVNGVFIPVTAYLMQRFTTRELFLSAMAAFLAGSTISGIAPGFEVLLAGRLIQAAGAGIIMPLLMNVVLAVFPEEKRGGAMGLIGVAIIFAPAIGPAYAGYMLDHYEWRSLFYVIIPFAVIVIIMASLYLKNVTERTHPKLDISGIILSTLGFGSLLYGFSRAGAIGWTSREVLLTIITGVISLVLFSISQLSKSSPLLELRTFKYNMFTLTTIINIVVTVVMYADMMLLPIYLQNMRHYSAFDAGILMLPGALIMGLMMPVAGRLFDRYGAKWLSVAGIAITVVTTISFTSLTDTTSYTYLVLMSTGRRFGMALFLMPITTAGLNQLPSALHAHGTAISNTVKQVAGAIGTALLVSVLTHQAQTHAIKLAAAGTISDPAQLLQKASIAGMNDAYFIVIIFGLAGLALSFFIRKTTQADSLQIPSRSNE
>NZ_CP009285.1|WP_042216287.1|5774424_5775300_+|SDR-family-NAD(P)-dependent-oxidoreductase
MPKHPTVVITGATSGLGQLVAIQLAKRGYHLVLTARSKERAEQTRQIIQAHNAKVNIRFFFGDLSLMQDVNRVGAEIAAACPVIDVLLNNAGLHAFEPRTTSEGLPEMIAVNYLAPWLLTHRLELPLRNAGKARVVNVASEASRRHGVLSLPGDLTDTTTFTARGSSPIYGKTKLLNIMFTAELARQWAGSGISVNALNPGFNVTGLGRELRFASVLERILKLLRLGDPQRGTDIITRLIVDQHYQEVTGGYFNVGTGKPIVPVSPGGDQAVQRKLWKDTQDLLDQRGYLR
>NZ_CP009285.1|WP_042216285.1|5773805_5774258_-|MarR-family-transcriptional-regulator
MKQSQHHNPPREELELALGAQLNALISASHALNVKAAARFDSSLQPAAFHIIRWLYSYGPASAAAIAEATAMDRSSVSRLIKQLESMGYVRREASPDDGRAILLSLTELGHQQTLGALNEKGSVFYERIAGWNDYELHQFINMLKQFNGL
>NZ_CP009285.1|WP_042216282.1|5770837_5773681_-|glycosyl-hydrolase-115-family-protein
MKSNEDFILAAPDQAVQIYLDPKGTDYNGLRRVADSFGADIKLVSGITPVMITQLEQLAGTVVIAGPIGGNELIDRLIAEGVLDVTAIQGKRECFRLQLVEAPMPGVDRALVIAGSDKRGTIYGIYSISETIGVSPWVYFADVVPYRNTTLSIPVSRLNRSSREPSVKYRGFFLNDDWPSLGSWVTHAFGDFNEDFYDKVFELILRLKGNFLWPAMWSAEFSLNGKSSPIANAVHADEYGIVMGTSHHEPLFRAGSEWQKVYAQYGTSNRWDFARNPQAITAFWEDGIKRNRHYDNLITLGMRGESDSALEGSDQENIELLKQIILTQKALLKKYNLEHMPQVLAVYKEVEKYWYGTAEVQGLKDWEVLQDVTILLSDDNFGNLRKIPEKHEQQREAGWGIYYHFDYHGGPHSYEWVNVTPLEKVWEQMTMAYDYGIRDIWVVNVGDLKPMELPLSYFMDLAYDFAGWGTGAINQTEEYTRRWVEQQFGSDLTTGTVDGIAQVLADYTRMNGRRKPEIIRADTFSVLHHQEAKRVLEQALSLEQAAAKYELKLPSPLKDAYYQLVYYPAVASANVIAMQIYAGLNNLYAERGSILANTYADLAERAIERDKQLEQHYNTGISGGKWQGMMSSPHVGYVNWNADGWSYPEVTRVIPAQEAIMIVGVEGTEQGYTAGTAGLPAFTNLQQESYEITVSSGGAGFEYEAASSADWIRLDRTQGWIDSGVTIRVSVDWEKVQGAASGHITLSGAGNTVTVQVTLEWTSLTNMPPVTFIETHHTVSIEAEHTASRVAKSGVEWKTISNYGRTLSSVKMLPAGISFDQPEEAPYLEYRLLVHQDGEYSLTAYIAPTNQLSPVSGLRYAAGFDGETPVTADALPPNYEGGNHDNEPWCRAVMDNIHTQVTRHRLDKGQHTLRVYGLDAGLVLQKLVLSSGPLPYSYLRPVESFHT
>NZ_CP009285.1|WP_042216281.1|5769093_5770692_+|response-regulator
MFNMIIVDDEERARVGIRTLIDWQAHGITIVAEARDGQEALDILGTHQVDIMLTDIRMPQMDGLELISIVSGKYPHIKSVIMSGYDDFAYAQQAIRVGASNYLLKPSRRQEILSTVLDITEQIQSEKLEIKSLEHLRQGFRESLPLLKEKTLSQLVLTESPAYPRLLANLKMNNLVFPYLLYGVILLRIDNFRQLHQKYLHEDTELLKYGLKNICEESLPETIVCIAFEHQDDIVLILNTDELLDHEELSGYIRIIQDNILSYLRFTVSAGIGSIDKNLQHLRRSFLEASQALNTRNYTGTGKIVEFSGEFDDEASQSSYPLHEEQEVLKAVRNGSPEEIAGKLTLFNVALQPETVSRDQVIKSSLALFFALYKLCIENNVNVNKVFGQNLTELIQVLSRSSLDHIFQSLLETALLVSEHLTSKKNSNKLLEAAKLYIGQNYMKDINREIVAREIYITPGYLSLLFKQQLKTSFTDYLHKVRIEHACLLFKDPGMRIEDIALQSGYNDTKYFYQVFKKYKGITPNQFRSNAE
>NZ_CP009285.1|WP_167549568.1|5767143_5768946_+|histidine-kinase
MLRFYLNMNLRYKITILIFLLITAVTFAIGGYSYSISKKQIINKVSNSNQSVLKQIDSNLSRMQKTIADWVTVFSLASVVQETLRSNTPDSVEIEDQFYNGPTASMMNQMLVTGNFDYLALYGSLSAPMFQVATDDSSGAYGLDKITPHNIYKESVALNGASYWFPLTEENNVFIQSNRNDKLGMTRIIRDIVNGNRIGFVFVGINLETIRRTYLTDLYDQDHGILILNESGEQLLAAGKETNDKKAVDFVMKQAEAGIMSGYTIVNLQGADTLLNYNINANGWITLYSVPLSSLTEELNSIKSAVLIMILASLVLSIPLLMFFSSFLTAPIKTLLLSMRRFQNGQFEEKVNIKYWDEIGQLSRGYNNMVANIKALVDDAYLLKLKEQEAELKALQSQINPHFLYNMLDTIFWEAEAAGQDKISEMVINLSRLFRLSLNQGKSFTSVAKEKELIELYLSLQKMRFKDSLDFVIDIPEELHPYVILKLSLQPFIENALIHGIERKRGGGCVSISGQLTGDQLKFVIEDNGGGMSSETLQKILTLPDESDIYTARDTGGYAVQNVQARLKHFYKGDFTLNYTSVPGEGTRVEIVIPAILNDI
>NZ_CP009285.1|WP_052429629.1|5765608_5766955_-|extracellular-solute-binding-protein
MVMNTKSTRNLLLITALAAVSVLSACGGNDQNDSAGSTNGNAADPAAEQVTLRVFSNLPDRKSGQGLAEQMVIDNYTKENPNVKIELETLAEEPFKNKLKAYMASNEALDITMVHGGAELNTLVQAGYVKELDPAGYEGETYNFLPGVYKSFTFNDKLYGLPRNSDYEVIYYNQKMFADNGVNVPTTYAELLDAAKQFRDKGIEPMSVNGKDLWSFAAFFQDLVIRVSGDQSLMLDAVEQKKNFTTDESFITAAKLLGEARDAKLFQESFMTADYGASQNLFTQGKAAMWYMGSWEAGMATNESLSEDFRNNVAVLKFPVVDGGKGKDTDLLAWNGGGYSLVSSSKHPEEAKKFFDYLMRADQWAKTVWDTGAAVPAQKYELTGTESGLQKQLTDVLTGATTTAGSLGLDYGTPKFKDDGQNAFGKFFAGGSTPEELLADLQKAAESQ
>NZ_CP009285.1|WP_042216297.1|5780562_5782374_-|heparinase-II/III-family-protein
MNRQELAGIVEDMKPADWSLYYPQGDSAAFWTRALSSGVLKADISEIRAEAQRLEGQPISALTYTLFSIFARTGSRLEYERVYFERRRRLNTYAFLSLLEPDRAEFLEKLEDILWVICDEYTWCLPAHLPAEHDAAEISRHIDLFSSETGFTLSEVSLLLGDRLPLLLQSRIRYEVERRIFRPFLEQGPYFWETSRHNWAAVCAGSIGGAALLLVKDAAMLTDILMKTESSMNYYLEGFGEDGACLEGLGYWNYGFGYFTYYSDLLRTSTGGRLDWFKQEKVSQIARFQQQCFIDESHVANFSDSVPQVRVHMGLSHYLADAYADVLRPPSALRAPFTDDHCSRFAPALRNLIWTRAGRENEAWEAASCYLPDAAWLLSRHVPAAGAFGFAAKAGHNDEPHNHNDLGHFILSGRGEIYASDLGSGEYTADYFGAGRYSYDCNGSQGHSVPVINGQYQGAGREFSAAVLHASAAAEKDELTLEMAQAYPVPGLQSLVRSLVWHKEELPRLELTDRYRYEEAPASWTERFVTWRRPKLLHPGSVLLPGTTGLGVEVTYDPEAVQPEITAHVYRDHYGQETLWHSLDFHVLQPGAEGTLAFTFQFL
>NZ_CP009285.1|WP_042216299.1|5782450_5783593_-|DUF2264-domain-containing-protein
MNGKEQRKYWLDTMLLIGGPVLEALAKRKLKEQLPTEFHSDRSQFAHLEAFARLACGMAPWLELEGLEGEEEQLRVRYAGLMLEAIDAAADPQSPDYMEFKTEGQPLVDAAFLAHALVRAPKAITGQLTERVKGNLITALKQTRRTAPSGSNWLLFSAMVEAALYILGDPDYDRMRVGYAVHMFMDWYKGDGVYGDGKDFHWDYYNSFVIQPMLVDVVALFEQESVQYAALKPLIMERAQRYASVLERSIAPDGTYPFLGRSIVYRFGAFQLLSQAALQHFLEEALPPAQVRCALTAVISRIMSYPGTLDENGWLRPGIYGYQPELAESYINTGSLYLCAAVFLPLGLLPSDPFWAGEELKWTALRIADGENVMRDHALE
>NZ_CP009285.1|WP_052429630.1|5783814_5784651_+|helix-turn-helix-domain-containing-protein
MKHAQYYEPFAGDILAGIGNSPISPTRDFHIHDHYEIFLFLGGNVNGFVDQFSYPLQRGNVLLFNNHEIHKIINLSSEPYERLTIHFKAPLVYPFCTATTNLLACFQNRQPGEHNLAHMEEPLLAEYLALASLLMAALKSGQYGSEVLALTYLIQILVIVNELYSRTRSAVPSIISSHIQSAMSYIDNHLHLNLSLEHIAGELNVDKYYLSHLFKQQTGGTIYRYVLLKKIALSKQLLSAGNSVSDTCYLSGFNDYANFIRTFKNITGIPPGKYGKKS
>NZ_CP009285.1|WP_081972169.1|5784977_5791652_-|S-layer-homology-domain-containing-protein
MTSKTRVKKRLFSVLMSGALVAGMFPALGIPAASAATVNTVYAAAYMGAKTTAGTTLPASVDVGGQSAAVNWSIGEDTFDVPYDTVTVNGTANGGPVTANVEVIPPAGSPLVYFVDSGRGGDSLNNPSGPSPLYEAVKTLSGGSLLNGLPDQKYINGQTDWGFDDNGNKVKNSKDGNLADPATEPSIWKVGLRADPSGNHIVYKLKALNAGTYTLSSGFYDWYGSRDRVIQPRLEYMNVSGETRSIPFTQFNSKTTQLISAEFTIPGDIDVSSPMTLTYAYVSGEKPILSWFAVAKGAIKQELDDARQTAASTVKVLLDGNDIQADNVNGLTFKGFGVLSGNSTSALLMDYKSAQPEAYAQLLQVLFGGDRPLIDHVKIEMGNDRNNSTGPDPSTMRTEDEAANVTRHPGFQLAADAKAINPAVKVSFLRWNAPAWANNNDKIYTWYKNTILAAYREYGYMVDYVNPDVNEHAADLAWIKQYSAKVKADSTGFKNTEEEELYHNIKLIISDEVGIGTFGDAMVSDLSLREAVTAAGYHYNTDDDSKGNFKRLAEEFDKEIWNSEAQATFSNSAFRPNNNMKDPSAAGTGIGGTGGPLEMGNTIIKGFVNSRRTHFIYQPAIGSFYEGGQYSFKELLSARDPWSGWIHYDAGLVILQHFNGFAKTGWENEENTAGIWRAVPKASYTGATGTNPVSGRNGTPSYMTLAAPDKQDFSTVFINDSEYEKIYKLQTVNMGYTGNPSLEVWETRAADQGQAFNSNYMKYLGDVTADGSGVYTVRVKPFSIVTVSTLDNHATEGQPAALPVEGERTVLDTDATGSVQNTEDGILYADDFNYGDKTVAVIGEGGEITGEQSYVSSRGGEQSVIPRYTQDLNGAFEGYRIGDTDNYVLRQQLDQNTTGVGGAWNGGDPVTAIGDNRWTNYKVSADVSFEQNSTYSGNNYAAVGARYQGGPQTLSGTPYALKFWFDGGWQLLSSGTVVASGNAATGAGGVKIAGFDTAHDAWHNIALQVAGDRITAYLDNVELKTYTDPNPKLSGRVQLASGFYHVRFDNLKVEKVDGYTPYYSELLDNLEMYDLAAVPGAKLVYEGAWAHENGKGMYVYQRSLSTSQAAGAVLKYTFTGTGLDILGQNDGSAKLEVSVDGRTVVLSGAAAASKELYQTFMLRGLEYGEHTVQIKVLSGTLAVDSVGVIDGGAAGNVNTAALELAVKAAQEITRQDEFPESDWNLFSGALGAAEAALNNPAGYRLDQEGAAQLEARLTSAYIGLVVGDVRELAAPQDTATYAGKKPDLPARLEATRADGSKVQVTVKWNVDAVSFDTPYERVAVTGTFGNLKTTAYVEVVPEGLLYFLDPGVSADGDTPPYTTIKNFVGNSLLNNKADQLSTDDTVWGHTNITANYSPKGIGGAVVATDKAQTGVYSSNTKNTPLVYKLPLNAGKYTITSYHLDWWNNSSRTMDITLSYADAEGKAVSEKVRTGLVAGPAGTAVNHDFTLPVNGTVTYSVYNTFSQAAVISYVAVARDKVSVANEQAVNEAKSIIEGAAYDVGKETANSEEAVQAWLVQTINGLPGFSATGVTMSDITLSPFQEATDDMDGSFTFSVTLSKGEAKADSSASGAITLPVPDTVLPVINLNGEAIVNLPVGAEYTDAGATAVDDQDGDITGRIVTTVTSEVYGLAELDTAVEDIYTFHYNVSDNAGNSAEEVTRTVVVALDPDVTKPVITLLGEESIQLENGVSYTDAGATAADDRDGDITERIVATITKDGESVLTLDTSAAGTYLYHYNVTDTAGNAAAQVTRTVTVGEAEQPPVTPTPTPEPEPTTAPTATPAPTDSPVSTVAPTPAATPSPAPQPQTEKVLGTGDFAAPAGGVITVQLTDATESVLLPAGLSGITGENTLRLAWSTVAVDLTPEVLKSIQEKVTVAGEQPEGARIKLSAVKTAKAAAEQLMNNPAVNGSVQLSAASDVISFSLEVVAADGTAVPVTAFDQPLTLTFTVDPNANRSLLGVYYIAASGALEYMGGTLADGKFTADVQHFSQYAVLEYNKSFVDVSSSNWANSVIKSMAAKHIIEGISATEFNPQGEVTRAQFAAMITRALGLKAGSTPAFADVDSESWYAGAVAAVNEAGIVLGRSKDSFAPNEHITREEMAVMIVRAYEYLQGSQVSQVSQVSDTAAGAFSDYSLIHDWAKNAAGTAEQAGLIKGRGNQQFAPQESMTRAESAQVIANLLGHL
>NZ_CP009285.1|WP_081970085.1|5791809_5792649_-|carbohydrate-ABC-transporter-permease
MVGKSKGLRISLMVLVYILLFATVLAMLVPYIWMLSSSLKLNKDVFSFPMQWIPANPRWENFTDIWTRIPLGRFIFNTAKLSIIVTILQLLTSSFAAYAFSKLHFRGKNFIFLGYIATIAIPWQAYMVPQFILMRYMGLNNTHLAIILLQAFSAFGVFMMRQFYQGVPDELCEAARIDGLSEYGIWARIMLPLSKPALSTLTIFTFVATWNDFLGPMIYLTDTKLKTIQIGLRMFISQYSAEYGLIMAASVVSIIPVVIVFLALQKYFVQGVAASGIKG
>NZ_CP009285.1|WP_042216301.1|5792664_5793603_-|sugar-ABC-transporter-permease
MQNETILHTNKSPKRRMSRGVKDNLIAYSFIAPNFIGFALFTLVPMIFAFILAFVKWDGANPMKFIGLDNFTRLIKDSTFHKALWNTVVYTIGVVPLTMIVALALAILLNQKIMGRNFMRTVFFFPYVASLVAVAAVWNFIFSPTMGPINNILHTITGIPLEDLPRWAADKQWAMFTVVLFTVWKNMGYYMVIYLAGLQGINPELYEAAELDGAGPWRRFRNVTVPQLAPTTFFVLMILVINSFKVYDIFINLFAGADNQLNDSTRVMVYQIYNTAFRSLDYGYASAMAIVLFLLVLGITIVQFRGEKKYGQ
>NZ_CP009285.1|WP_042216303.1|5793758_5795102_-|sugar-ABC-transporter-substrate-binding-protein
MNLKRFYGMTLATALSVSMLAGCSGNNANNEAAATTAPAAGNAANASAEPSQEPVTLKWALWDWEATAYYKPLIDAYKAAHPNVTIEYVDLGSTDYMTMLSTQLSGGADLDVLTIKDIPGYSNLVKQNHLEPLKSYMSANSIDPSVYGGTVEQIEVNDEVYALPFRSDFWVVYYNKALFDKAGVEYPSNDMTFDQYDELARKMTSGSGSEKVYGAHYHTWRSAVQLFGILDGKNTVVGGNYDFLKPTYERILKEQEDGIVMDYATLKTSSTHYSGVFYNNSVAMMNMGSWFIATQIEKVKSGESQSTEWGIVKYPHPDGVEAGTTLGTITSLAVNQKSKHKEAALDFMNFVTGEEGAKVIASTGTIPAIKNDEVINSITSIDGFPTDENSKAALNTVQTYLEMPMHEKSADIEVILNEAHDNIMTKNATIDEGLKDMNKRVGELLNN
>NZ_CP009285.1|WP_042216305.1|5795364_5797155_+|sensor-histidine-kinase
MDKGVFTTVRKSTIKSRIILLMAVFALLIASLLSFFSYELITYYQRKTTIQATEFNLQLVSHIIEQDLINLSALAMTCSTNSSTNILITNYFASKNPSSKEAVNVFNSMQQEFLNNRSNSYARRLIVTDNNGKFLQVDNTGTSVPLTIHNIGHIAGLNAVAEEQWDQVIKDPLSNTNGIPFVFPIYGKGAVRVGTVYMLANTSVITDKLKGYSLPKNSRLLLTLGNHHYQLTGDQVTAITEPYEPVAYTNDKPVGPQTELSMVKLTDDKESHIVVSYPVRSGVILSQTLSNDQFAPKANIWILVMIGVVLLVIVLSAIITLYLTRTISLPVEKLKKRIDKIAQGNFLIDRNIEWKSELGDVGRGINRLSQDIVALMDSRLADEKQKQELEYRMLQSQINPHFLYNTLNSIKWMATIQNATGIAEMTTSLSRLLRSIAKDNRRLMPLKDELSLLDDYFLIQKYRYGSTVTMVKEIENEELLTGLIPRFTLQPLVENAIFHGIEPKGRGDIVITVSKSGFADILVTIEDNGVGMKEEQISTILSVPEDESKGMLENVGLRSVNERLQLAFGGNYGLSIESELGQYTIMKLLLPFLQRE
>NZ_CP009285.1|WP_042216307.1|5797267_5798899_+|response-regulator
MIKLLIADDEALVCIGLQSMLKWEQFNIEIVGIAHNGAQEEEMIDTLRPDIVISDIKMPIKSGLEVAGSVRKKYGRLPLFIMLTSYEEFQYARGAIEVQATDYLVKLELTPEALSESIRRAIGILETYQAMESYPKLVHRGNIQAQRDKFFIRLFNNLFENKNQYLLQKEDLDLDLPGAAYLVCTCRILGPDTVPPRGDKLVALCSSTVQMAKDTLSSVSPCYVTSLDLRNFAVALPVPETDPRLWMPDIQKLLGDMASVLHNYFNVTIIGAIGFAVEDPYLLRESYLAARKALPAAVKERSFVFFTEGEALAQEHLLFDFSESRSEIRRAFEEMDTRALYTIISRMIEIFDGRSDLLVPATDAACNILYMATSLLADGENIVEQIFENEPEGYRAIYQMHTIEEIAGWLIQFRDGCSDILSTRRQSYKEQVVKNVQEYIKRNLGSKLSLNQVADVFNFSPNYLSHLFSKVAKVNYVEYITEIKITAAKEMMVRGEGRIYEISQKLGYESAFYFSKVFKKVTGLSPRDYMQQIESGTEDVRSQ
>NZ_CP009285.1|WP_042216309.1|5799089_5799935_-|carbohydrate-ABC-transporter-permease
MNSKTAFRSIGQILLQIPLWLYFIVSIYPLFWMISYSLKNNDEIFVTNPFGFPTHFRFENYVNAWTQFNIPRYFMNSFVVSTISTLCILLLALMFAFAVARMQWKFRSAVRTYMIVGMFMPLQVIMIPLAILVRDFHLTNTFGALIIPYIAIGLPFSTMVFYGFLVSIPREIEEAACIDGASIYRLFGRVILPLALPAIATIAIFQFLNNWNEFTLAYILISDENMKTLPLGLLFFQGSYSTDWGAMGAVMTIASIPMVLVYLLLSEQVERAMTVGSAVKG

Crispr_ID: NZ_CP009285_18

• CRISPR_ID: NZ_CP009285_18
• CRISPR_location: 6904380-6904465
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_18

Consensus_repeat	Method
GGCGCTACGATTACTGCCGGTAC	CRISPRCasFinder

spacers of NZ_CP009285_18

>18.1|6904403|40|NZ_CP009285|CRISPRCasFinder
GTTAACTAATCTGCTAGATGGTACGATCACCAGCGTGCTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_18

CRISPR arrays

The CRISPR arrays of NZ_CP009285_18

>merge|NZ_CP009285|18|6904380-6904465|CRISPRCasFinder
GGCGCTACGATTACTGCTGGTACGTTAACTAATCTGCTAGATGGTACGATCACCAGCGTGCTTGGCGCTACGATTACTGCCGGTAC

>NZ_CP009285|18|17|6904380-6904465|CRISPRCasFinder
GGCGCTACGATTACTGCTGGTAC	GTTAACTAATCTGCTAGATGGTACGATCACCAGCGTGCTT
GGCGCTACGATTACTGCCGGTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_081972235.1|6894661_6895393_-|YutD-family-protein	unknown	unknown	gnl|CDD|368821
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350148
NZ_CP009285.1|WP_157764162.1|6891654_6892830_+|hypothetical-protein	unknown	unknown	gnl|CDD|377924
NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP009285.1|WP_042217350.1|6901837_6902416_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217343.1|6892870_6894322_+|S41-family-peptidase	unknown	unknown	gnl|CDD|223864
NZ_CP009285.1|WP_099052568.1|6904466_6905384_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|224561
NZ_CP009285.1|WP_042217351.1|6902440_6902977_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl|CDD|226063
NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein	unknown	unknown	gnl|CDD|200477
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	unknown	unknown	gnl|CDD|133029
NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042217345.1|6895714_6896620_-|lipoyl-synthase	unknown	unknown	gnl|CDD|235493

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042217343.1|6892870_6894322_+|S41-family-peptidase	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	1.11258e-90
NZ_CP009285.1|WP_081972235.1|6894661_6895393_-|YutD-family-protein	gnl|CDD|368821	pfam06265, DUF1027, Protein of unknown function (DUF1027). This family consists of several hypothetical bacterial proteins of unknown function.	3.80635e-48
NZ_CP009285.1|WP_157764162.1|6891654_6892830_+|hypothetical-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	5.75436e-29
NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	1.75741e-45
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	gnl|CDD|350148	cd18827, GH43_XlnD-like, Glycosyl hydrolase family 43 protein such as Aspergillus niger DMS1957 xylanase D (XlnD); includes mostly xylanases. This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have mostly been annotated as xylanases (endo-alpha-L-arabinanase, EC 3.2.1.8). It belongs to the GH43_bXyl-like subgroup of the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. The GH43_bXyl-like subgroup includes enzymes that have been annotated as xylan-digesting beta-xylosidases (EC 3.2.1.37) and xylanases, as well the Bacteroides thetaiotaomicron VPI-5482 alpha-L-arabinofuranosidases (EC 3.2.1.55) (BT3675;BT_3675) and (BT3662;BT_3662). GH43 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. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. 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.	3.63353e-163
NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.05153e-96
NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	4.40135e-16
NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	7.04425e-21
NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase	gnl|CDD|224561	COG1647, COG1647, Esterase/lipase [General function prediction only].	2.24581e-28
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	gnl|CDD|226063	COG3533, COG3533, Uncharacterized protein conserved in bacteria [Function unknown].	3.84504e-167
NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein	gnl|CDD|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	3.4844e-178
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.748e-12
NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	7.10427e-52
NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	7.39305e-46
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.05383e-71
NZ_CP009285.1|WP_042217345.1|6895714_6896620_-|lipoyl-synthase	gnl|CDD|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	0

Protein sequences

>NZ_CP009285.1|WP_042217351.1|6902440_6902977_-|hypothetical-protein
MPNDAVFNQNSQPLYTEQVNTYIAPGIDTLPEAGAAMSGLLFGYSFASTVTTAAPLVMQVSNPGGSGRTVYISRVIASTGTAAVTLTLLRNATVGGSIVTPVNYNFGSAVTSVTTARTATAAPTGSPATIMSLLLATGPVILDLDGRIILPPGNSLTINITIASGSTAATGNISWWEN
>NZ_CP009285.1|WP_042217350.1|6901837_6902416_-|hypothetical-protein
MPNNYVINDNDQPVYVEMTNTFRAPDISAPPEISASQSAVLFSANASNSATIVLGLASAIITVRINNPAGSGRTLYLSRVSGSIGGTSLLTSISGTFTIVRGGTITSPATVTPVNNNLASSAASAMTVQSSTAAITGGSVLATYQLAPGVFTPAFTGSIIVPPNNALSINVTSSSAAVGTIISALSLTWWER
>NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase
MMDSCLFIHGFTGGEYEIAPLSQILGAHDCLSRTFTLQGHGGSRSDLLQSDRQGWRQSAEDELNTLLTRSEGVHLIGFSTGALIASHLSVQYRARIKSLTLLSTPVFPLNPVQILRTLGQPAMIRNYIRKWGSTPAKATREFQRLVRESFEIYPQMDLPTLIVQGKRDHLVKFKSAGYLEQTIPSGRKQVLIMEKSGHMVCHSEESPAMMNEVLQFIRSSGN
>NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator
MKVTIKDIAQAAGVAKSTVSKVMNDSPKISEETKTRVRDIIKQMNYTPSSIATGLARQSSNTVAILIDMSKESEFLNQFFYNIIGGVESIIGPLKYELTIANIQHDHAEGHFLHRLVLNKRVDGIIANTSVLTPELCAELNRLEFPYISIGEINPPGTWVDCDNELGGTVLTKHLLEQGYSSVAFIGGEQNEPLFLRRIAGYTATLRQAGLPVRSDRIINGRAAEEDGYAAAMQLLQNPEPPDAIVCMSNFSAFGVLQAARELKIQIPEQLGIATFDEYPLSPYTTPPLTSLNMDTFQLGASAGRLLMDKLGTTATPVSGQLLEPVLIPRLSSLRSRK
>NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein
MPKRLFLYHTAEDPFAYPVGSGTLKLRLFVQSGQSLSCTVVHSDRYDSPGSELPQEMERIGSAGAYDIHEAVLRTGTGKCRYQFHIKNPAGEYVWYGERGMSENREQAGAFQYAYIHRPQATLLPSWSTEAVVYQIYPSSYNKGTLQGIADKISYLHNLGVTAIYMTPIFESPSEHKYNTSDYYRVDPGFGTLEDLKMLVDTAHRHGMKVLLDAVFNHAGDTFFAFKDVLERGEASPYKDWFYIHSYPVSKAPVPGYETFAKAEASMPKLNMDHPEVADYMMEVAKYWVREAGIDGWRLDVANEVTPAFWPRFRRELKAEFPELLLIGEIMHASGPWLRGDQFDGGMNYVLRDAVLEFFAAQSAGPVRFMEQLLHQEALYNDQANSAMFQLLGSHDTLRFLTACKLGGRGWDREATSLSRMKLAVFFQMTYIGLPMIYYGDEVGMEGATDPHCRQPMVWEAQEQNISLQEWYKQLISLRKEHEVLRTGGFRPWFTDEPRNVLGYVRRSEQDRMGLIINNSPNAYQLELCNYRSDKNVLTDLLSGLTIRADKRVLVEIEPFGCLMLH
>NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase
MPALFRSCNTRRTLLCMSAAALLWGSSPAVSVQAARYYKLPELTTTTNSPTAKDSKETAAAARKGLYEQMSAATGIPWFRFAAIDQYERSVAKKKKSPAPSEADSAEAPARLTGISIPAPVWSGPLNPDQEDKFPESITLFGGFGRDGTGDGIADPGNDVDVLYSMAEHLLKYGRSASDFSIGVWEYYHNGRAAQRVAQFAKLYEHFGRLDLSGSAFPLPIGTNYAYRSTWGTGRSWGGARIHEGTDLFAPHGLTVRSTCFGVVETKGWNRYGGWRIGIRDIENRYHYYAHLMGYEKSLSRGDIVIPGQTIGWVGSSGYGSPGTQGKFPPHLHYGIYRDRGITEWAFDPYPLLKQWENQEYRQLKKNKNKK
>NZ_CP009285.1|WP_042217345.1|6895714_6896620_-|lipoyl-synthase
MTNRTAKQPKPDWIKIKLTTGEDYQEIKGMMRSKTLHTVCEEARCPNIYECWANRTATFMILGDICTRACRFCAVNTGLPTELDLLEPERVAEAAEGMMLKHCVVTSVARDDLKDGGAQIFAETVAAIRKRLPLCSVEVLIPDFLGDRGSLEIVMNSNPDILNHNIETVERMSDRVRARAKYRRSLELLRRAKEIKPDIPTKSSIMLGVGEEWDEILQAMDDLRAVDCDILTLGQYLQPSPKHLNVEKYYPPEEFAMLKEEGMKRGFSHVEAGPLVRSSYHAHDQVKSAAVAREARSVSQA
>NZ_CP009285.1|WP_081972235.1|6894661_6895393_-|YutD-family-protein
MIVIGGKGYELMLDHKDGWNPEAFRGRYSEVLDRYDYIIGDWGYSQLRLKGFYRDNHPKVNRDTAISGMVDYINEYCNFGCAYFVLHKLKEAPQEGTFKDILIKEVPEPGTEEELEQEAAEPAVNVKDHRESPSKGGNQAASNRDKDHAGGSSREHAAKDRPVREHQSRNHRNKDGQGKKNHKEFQGRGQQGNQGNQGSNQGNPNNHKQNKENREHRENNPNRQNNQNKQDNPNSQNQNNSQA
>NZ_CP009285.1|WP_042217343.1|6892870_6894322_+|S41-family-peptidase
MKPAKILTAALSGCLALSIAWAPAASAADAAASTEAAQSSKTDIINEIMEYLEYYNVEGIDQDTLIRGAIDGMVSTLEDPYSQYFDQAEAADFGHAVDLEYVGIGVRLVYTPKELYIEEVMSGSPAEKAGLKRGDTILKINGVRVDDTAGDELAGASGTKVTLLIQRNGVSKSYSVTRSEITTSSVTSTIIGSKIAYIAINGFTQTADEEFSTALDKMRAAGMKSLVLDLRDNTGGYMDSAQNIAAKFMDAGIMMYTSDQSGVLTPVTITNGSKIGVPVVVLTNEYTASASEALTGALRDNKLATIVGTRSYGKARIQSLIPVSDGGELKLTTMKYLTPSKEDFNHIGLAPDLEVKGKTAQLITALQIAGLTGITASGDNHILDINGAAFAGNVGLVKQGDKVYASSRALSALVESEVSWDAKNKKVLITTGAGTSYGFTLASKEALYQDGETFIELGAFKKKFPLLTWSYNAAQNQLKLSVK
>NZ_CP009285.1|WP_157764162.1|6891654_6892830_+|hypothetical-protein
MKKLLSMIGVSLLALVLAVPAFAAEKPIKVYINNSNLTFTAGTPYLKDNTVLVPFRVIFEKLGLQVLWDAKTGTVTGTGTGLNISLKVGSKRATVNGTVKQLTVAPVSTAGTTYIPLRFIAEATGGTAAWDAASRSVKITVPQSSSSDEKDITALIQLSNKYYNEEKAISFYSLVDSESDNMESVTDMNSLFELYDLKNTIQSLKILSIAGNEATVYTVEKSVRTGGYYIPDEQFEYLYTLVRKDGSWKISGMEVQESTVLLTREQGMKQAVVPQSDATVIKDNLSKYYQNMTTQNVDGTMALMTSYGEDYDAASAADLQDLFDSYDLSYSLTNANIYYYAADEAAVYTEVSIKDGESGESYTQSLIFILTKSESGAWTIDDTYHISFDSL
>NZ_CP009285.1|WP_099052568.1|6904466_6905384_+|hypothetical-protein
MSSAGTVTNILAGTITSVLGATITAGTLSSAGTITNILEGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSVTSISQRSFIELATTGIATSDTYTPLPANTTSVLGTYSYFIVNTGANPINTRVEISADGTNYFVDTTGDNPLPAGSVDVIVPARFLKYTRLSYQSSTPGAASTLNVIFDAQGT
>NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase
MNKPAKPTLGVQLIVKNEAELLPRCLASLDGADEIIVTDTGSSDQSVEIARAYGAAVYEVQWSNNFSAARNTGLSNANTDWILVLDADEILQTSIESIKDILQDSTAEAYTVRIENWLGSNPEDRLYHSNVRLFRNGQGYLFSGRIHESVDSSILKSHGAAAIGTSSIEIIHLGYLPSIMSAKNKTSRNEQLLRLALEEEPDDAFYSYNLAVTCCQDGRLMEAEELLLHTLGHAPLQVSYRPSMIRDLCKIYLATGKVKALDSLLTRELMRYGDYPDLHYIQGQSWESQGLPDRAYQSYQHAVDTSSAPAPRRAYVSEQGMDSFRPLHRMGVISQQLGKQEEAARLFHRSLQHHSLYLPALQGIASAFQQLKVPDEDIAGLLIQLAGTGQSAARAAIISTLYELGAYKAIAEQPPELFPLEADTVLLILSSWISTGKYHAFSKTAAKLRAQSLQLSPGGLNTETMRQLWLLEAVCTWELGEALQQEKWLQSPAELRSGLLFIDTQLSSEAVLPQAAVADSVHSPLIHEVIRLAVKLELVTLGKQLVDRFPAHTGDLAEVLYEEGWRAEAGELFIRLVSSKEARGSTLRYLGEMLADKGHYAEAAGWYRLSLEDSPGNEAVLAGLSLCYLHLAEQGLGEVANSFKGEHAHGPLQEDRAAIAHSITVLNRTPWHTVWNYKQRQRGADLSL
>NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase
MKKTPRKPLISLCMIVKNEADTLARCLQSVRGVADEIIVVDTGSTDSTVSIARSFGARIIPFTWNGDFASARNAGLAVAQGTWILVLDADEELEPGSKKELLVCAEHTEYEAFFVRIHNHKGTDRASQTITVNPILRMFKRRVNYRFSGIIHEQIAAVIVQETPAAAMHMSTVVVHHYGYADGVVEKKDKISRNIGLLKEQLKLNPGDAFHHFNMAVEYMRLGDYGHALEHIQTSLDLVEPDTSYIHLLYKYEIRCRAVTGDLPGALEACERGLALFPDYPDLHHIKGALLLQVSAFAEAKAALGRALDIGVSPPAYHTESGLGTYLTRTLLGQVCQQIGEDNEAIACFTRAAQLHPEPLPLVTRLVRLFKCAGRELELKGWLAEHLPAILAEQRQELVRLLVTDGCYAAAADVLGGGVGEGVAGERSAGERVMREFGVGELGEEEQVVREFRAGELAAEEQVVREFGERKLAAGETVARERGEGELAAGETVARERGEGELAAGETVARERGEGELAAGETVARERGEGELAAGETVARERAANKRSSGAHAENGHDYAGEPEAASSDSLFLLLQRAEAIPAAELKHGDIAALLQHPAIARTTPATESAASAVQPWISLADKLLATLEASSVFSPAAARARLALPLPRPAD
>NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase
MLIPGLSLCMIVKNEAQHLEKCLLSVQGLVSEIIIADTGSSDESIDIARRFGARIIELPWEHDFSKARNLTLRLASCTWILVLDADEALTDWRPEEVERLLETQSADGYFLPFIHYVGEFSEGDYVTDNVCRLFRNDERILFRGSIHEEVASSIWSLPGGNIAYTALPVHHYGYLDGELQRKHKTSRNLELIHSALKLEPHSIHLRYALGTEHYQQGNYNAAAEVFLPLLEEVPADSGYTADLYLKTAFALEAGGRPEEAQSVYEAGSILYPDFTDLLESYAGLLLEQGELWLAYDLLQRALDSGDTAYKYPSSSGSGTSRTRLFTGQVCERLFLYEEALDHYRQALGYTPDYSAAWEQLAPLCLLSGQEEQLTAITRQLLPALPQRVLGRLVPAALNARAAEWLAALSAAPHLPEAIRQVLQVLLGTLFRDPEQPSTASVRLERMLRDEPDQPWISGYLWALSCRSGGPAAAGQWLERLARNRPGIAAMHRWLAQQNGGAPAHLAEREPDAERPADQPADGAGTDRRFKGTVRHPDSSNSALPQRTAEDYTDSSVPPPGSSSHPELSADTPLRFPDISYTAQLLVQAGAWDTLLLLFSPMAASRFQWSRLPQPLLHGLLQAPVPVKEQWCAMYTGQAHFYSSPGDAAEWLLYAAIADSCGLIPRLDPADEQALRQSGGTAAAVGLSYCQLLLAAGVHPQGMPVVSGSIPWLLLARSALQAE
>NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase
MHEPLRKASGNRLTAMMQVRNETGRYLEQVLEELSGFVDDIVIVDDGSTDGTVRLCNSFAKVSKLVTLEHSIFGREWELRKTLWDLAVSTGPDWLLSVDADEFYEDRAKQEMRRLIDQDAYDWVAFRLYDFWGGTTHYREDEHWNIHTKHTRTLVRYLPSFYYFTPRMDHHVPRLPLSYAVLPGFLAELRVKHYGWALEPEELRRKYDRYMELDPEGKWGSLEQYRSILDVDPRLVEWRE
>NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein
MNYIVLSRVSWEDYEYKRLLELLPDRGEVCFAGRMTPVQQRSSGIRSVTLAEIYSLNAGDYTLLVSSPYWLPDVLALQPAYTVALLELCPEGEDSVLWDKYSALLAAKADLAGTTSERIYLEQNLRRKGIVYLSGDQPLSYGLLRREEQLFFLSDYEAIWNRALTELWQPPVDPDGESGWLDIQRRHRTAFYISMCAKMPHQPSVHYLAASYLYLRGDEAASLYLAQSFELMLLHDYTDCLHSHYRFFSAIEAKKGNLELAVRQYEITAFTAEERAKAAQMKQWLSGGEVEHELLRAEILTVNEDGAAANEILSRLTGPEARQRLLLNYIGTFQWLKALQLYHEMEADGTVAAENTGLGGFAGIAGIAGAPEIPGLAGSISPAFEGAVQLPVIEGTLHLLYGRRHDAIRSFLRSAGADQGARQLFAEMADMEEAVQGLRGRAMDGEEHA
>NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein
MSYEAMDAINTIKVMNTVKAVSTERLAGRYSYLEREGLLPLPVQGGVTLVVELRHAQWSAECLRLLLQHSGSSVRLIAVPMTAEFPLQPLSEQFSGEPSLVFLPFAAGNYRVNEALAYAETSFVVLLEDTVMVSPGWLGNLLWPPIDDPVVGVVAPRSSSEWGEGLERLHFAGYSELSAYVAHTLDKRQGEWSYADVLGGACLLMARDVLLRVGGFDSSLVDRRLIIADWCLRARMQGASLALSDPVYVHVLHPLEEGAAENNASNAAASEGEQAYRRKWNLQGSPAAAGPLQIPVDLSGCLPQPSIPLGRHTADTPLVTTVVYFEENWTAADSRERQQTLQEGQSYSNIRWVWVRDSWSQSFPEFPVHERDAVITVHGEKPWLHALENISALYGSEVVVYLSASAAYDSRYIEKLVEILQHSRADIVVSSDFAADEPGQRPETGGITQLLPLERIAHRSGITPGKLMKREGFLRSLALIPDPDLSVGYAGELAGGRDKIQPSAHGGEGHL
>NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase
MTNPIVPGWYADPEARTYHGRHYIYATRSFTEYTRQMNLDAFSSEDLIHWKVHESIIEMDDFPWIWRAVWAPTQIEHNGRYYLVFASNDIQKDGEAGGLEIAVADAPEGPYRGYLHRPLIGEFIHGAQPIDAHLFKDDDGAIYLYYGGWGHCNVCRMNEEMTGFVPFPDGQLIRSVTPPGYVEGPCMIRKDGLYYLMWSMGGWTNGTYRVAYGVSGNPLGPFDNQGTILERQEPVAEGPGHHGYLYLPDRDEWLIVYHRRIIGDPEPGNRMLCIDRMEFAAGGIKPVIMTDRW
>NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein
MAEQQPKLHAWQGVSFTSITINDHFWRPRLEVLRQTTLPDCLSKCEETGRIDNFAKAGGLMEGHYEGKYYNDSDVYKVLEGIAYALMPRRDAALEAEADRIIGLISAAQEADGYLSAYFTLENPQGKWTDMEKHEMYNGGHLIEAAVAYYEATGKRGLLEVACRLADHYDEVFGPGKRHWVEGHQEIELALVKLYRVTQSERYWKLALWLLEERGHGHGAGAIWDNPEWGPAYCQDDVPVREIRQVTGHAVRAMYLYTAMADIVHASGDSAYAEALHRVWAHTVERNMYVTGGIGPSRHNEGFTSDYDLPNETAYCETCAAIAMVFWNHRMNLTFGDGKYADVVEREMYNGALSGISLSGDKYFYVNPLASQGGHHRVPWFETSCCPTNLARFLPSLGQYVYAATEEGLAVNQYLNSEAELVLGSGLGVRLKQSTEYPWDGRIELEVNPASSAGFSIRLRVPEWCRSYRLAAGGVSISGAGALTDQGYLVLNRHWSPGDKVVLELDMPVNLVRANPEVEADRGRVAVQRGPVVYCLEQTDHPGLSYDACSIPAGAKFRVEHLPELLGGVTVLQSRDEAGRPLRFIPYYAWDNRESGFMQVWIREQEERGLYSC
>NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease
MFVIPFVWLIRSSLMNLSQIFTMPPEWIPKPFQWSNFHKALTVLPFDVFFKNTLIIVVTVLVGTVITSSIGAFGFSRIQWKGRDTVFAILMTSMMLPAAVTIIPSFLGWQLMGLYDTLYPLIVPAYFGGGIFNIFLLRQFYLTIPRDFDEAAFVDGANYWQIYTRLIFPLSRSAIIVVALFSFLASWNDFMGPLIYLKSDSLFTLALGLQMFQGTYTAQWDLLMAASATVVLPCVIVFLAGQRYFLEGITLTGLKG

Crispr_ID: NZ_CP009285_19

• CRISPR_ID: NZ_CP009285_19
• CRISPR_location: 6912843-6913136
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP009285_19

Consensus_repeat	Method
TTCAGTCAGTTGTTCAGTCNGNTGTTCAGT	CRT

spacers of NZ_CP009285_19

>19.1|6912873|30|NZ_CP009285|CRT
CAGATGTTCAGTTAGTTGTTCAGTTAGTTG
>19.2|6912933|18|NZ_CP009285|CRT
TAGTTGTTCAGTTAGTCG
>19.3|6912981|30|NZ_CP009285|CRT
TAGTTGTTCAGTTAGTTGTTCAGTTAGTTG
>19.4|6913041|18|NZ_CP009285|CRT
TAGTTGTTCAGTTAGTCG
>19.5|6913089|18|NZ_CP009285|CRT
CCGTTGTTCAGTCCGTTG

CRISPR arrays and Neighbor proteins around NZ_CP009285_19

CRISPR arrays

The CRISPR arrays of NZ_CP009285_19

>merge|NZ_CP009285|19|6912843-6913136|CRT
TTCAGTCAGTTGTTCAGTCAGATGTTCAGTCAGATGTTCAGTTAGTTGTTCAGTTAGTTGTTCAGTCAGTTGTTCAGTCCGTTGTTCAGTTAGTTGTTCAGTTAGTCGTTCAGTCAGTTGTTCAGTCAGATGTTCAGTTAGTTGTTCAGTTAGTTGTTCAGTTAGTTGTTCAGTCAGTTGTTCAGTCCGTTGTTCAGTTAGTTGTTCAGTTAGTCGTTCAGTCAGTTGTTCAGTCCGTTGTTCAGTCCGTTGTTCAGTCCGTTGTTCAGTCCGTTGTTCAGTCCGTTGTTCAGT

>NZ_CP009285|19|5|6912843-6913136|CRT
TTCAGTCAGTTGTTCAGTCAGATGTTCAGT	CAGATGTTCAGTTAGTTGTTCAGTTAGTTG
TTCAGTCAGTTGTTCAGTCCGTTGTTCAGT	TAGTTGTTCAGTTAGTCG
TTCAGTCAGTTGTTCAGTCAGATGTTCAGT	TAGTTGTTCAGTTAGTTGTTCAGTTAGTTG
TTCAGTCAGTTGTTCAGTCCGTTGTTCAGT	TAGTTGTTCAGTTAGTCG
TTCAGTCAGTTGTTCAGTCCGTTGTTCAGT	CCGTTGTTCAGTCCGTTG
TTCAGTCCGTTGTTCAGTCCGTTGTTCAGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|224561
NZ_CP009285.1|WP_099052568.1|6904466_6905384_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_CP009285.1|WP_042217351.1|6902440_6902977_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl|CDD|226063
NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein	unknown	unknown	gnl|CDD|200477
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	unknown	unknown	gnl|CDD|133029
NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_042217350.1|6901837_6902416_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350148

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.13425e-76
NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	7.04425e-21
NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	1.75741e-45
NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.05153e-96
NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	4.40135e-16
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	gnl|CDD|350148	cd18827, GH43_XlnD-like, Glycosyl hydrolase family 43 protein such as Aspergillus niger DMS1957 xylanase D (XlnD); includes mostly xylanases. This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have mostly been annotated as xylanases (endo-alpha-L-arabinanase, EC 3.2.1.8). It belongs to the GH43_bXyl-like subgroup of the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. The GH43_bXyl-like subgroup includes enzymes that have been annotated as xylan-digesting beta-xylosidases (EC 3.2.1.37) and xylanases, as well the Bacteroides thetaiotaomicron VPI-5482 alpha-L-arabinofuranosidases (EC 3.2.1.55) (BT3675;BT_3675) and (BT3662;BT_3662). GH43 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. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. 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.	3.63353e-163
NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase	gnl|CDD|224561	COG1647, COG1647, Esterase/lipase [General function prediction only].	2.24581e-28
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	gnl|CDD|226063	COG3533, COG3533, Uncharacterized protein conserved in bacteria [Function unknown].	3.84504e-167
NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein	gnl|CDD|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	3.4844e-178
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.748e-12
NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.83169e-50
NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	7.10427e-52
NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	7.39305e-46
NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.39726e-45
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.05383e-71
NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	8.79265e-81

Protein sequences

>NZ_CP009285.1|WP_052429689.1|6909588_6911757_+|glycosyltransferase
MLIPGLSLCMIVKNEAQHLEKCLLSVQGLVSEIIIADTGSSDESIDIARRFGARIIELPWEHDFSKARNLTLRLASCTWILVLDADEALTDWRPEEVERLLETQSADGYFLPFIHYVGEFSEGDYVTDNVCRLFRNDERILFRGSIHEEVASSIWSLPGGNIAYTALPVHHYGYLDGELQRKHKTSRNLELIHSALKLEPHSIHLRYALGTEHYQQGNYNAAAEVFLPLLEEVPADSGYTADLYLKTAFALEAGGRPEEAQSVYEAGSILYPDFTDLLESYAGLLLEQGELWLAYDLLQRALDSGDTAYKYPSSSGSGTSRTRLFTGQVCERLFLYEEALDHYRQALGYTPDYSAAWEQLAPLCLLSGQEEQLTAITRQLLPALPQRVLGRLVPAALNARAAEWLAALSAAPHLPEAIRQVLQVLLGTLFRDPEQPSTASVRLERMLRDEPDQPWISGYLWALSCRSGGPAAAGQWLERLARNRPGIAAMHRWLAQQNGGAPAHLAEREPDAERPADQPADGAGTDRRFKGTVRHPDSSNSALPQRTAEDYTDSSVPPPGSSSHPELSADTPLRFPDISYTAQLLVQAGAWDTLLLLFSPMAASRFQWSRLPQPLLHGLLQAPVPVKEQWCAMYTGQAHFYSSPGDAAEWLLYAAIADSCGLIPRLDPADEQALRQSGGTAAAVGLSYCQLLLAAGVHPQGMPVVSGSIPWLLLARSALQAE
>NZ_CP009285.1|WP_052429688.1|6907613_6909572_+|glycosyltransferase
MKKTPRKPLISLCMIVKNEADTLARCLQSVRGVADEIIVVDTGSTDSTVSIARSFGARIIPFTWNGDFASARNAGLAVAQGTWILVLDADEELEPGSKKELLVCAEHTEYEAFFVRIHNHKGTDRASQTITVNPILRMFKRRVNYRFSGIIHEQIAAVIVQETPAAAMHMSTVVVHHYGYADGVVEKKDKISRNIGLLKEQLKLNPGDAFHHFNMAVEYMRLGDYGHALEHIQTSLDLVEPDTSYIHLLYKYEIRCRAVTGDLPGALEACERGLALFPDYPDLHHIKGALLLQVSAFAEAKAALGRALDIGVSPPAYHTESGLGTYLTRTLLGQVCQQIGEDNEAIACFTRAAQLHPEPLPLVTRLVRLFKCAGRELELKGWLAEHLPAILAEQRQELVRLLVTDGCYAAAADVLGGGVGEGVAGERSAGERVMREFGVGELGEEEQVVREFRAGELAAEEQVVREFGERKLAAGETVARERGEGELAAGETVARERGEGELAAGETVARERGEGELAAGETVARERGEGELAAGETVARERAANKRSSGAHAENGHDYAGEPEAASSDSLFLLLQRAEAIPAAELKHGDIAALLQHPAIARTTPATESAASAVQPWISLADKLLATLEASSVFSPAAARARLALPLPRPAD
>NZ_CP009285.1|WP_052429687.1|6905550_6907617_+|glycosyltransferase
MNKPAKPTLGVQLIVKNEAELLPRCLASLDGADEIIVTDTGSSDQSVEIARAYGAAVYEVQWSNNFSAARNTGLSNANTDWILVLDADEILQTSIESIKDILQDSTAEAYTVRIENWLGSNPEDRLYHSNVRLFRNGQGYLFSGRIHESVDSSILKSHGAAAIGTSSIEIIHLGYLPSIMSAKNKTSRNEQLLRLALEEEPDDAFYSYNLAVTCCQDGRLMEAEELLLHTLGHAPLQVSYRPSMIRDLCKIYLATGKVKALDSLLTRELMRYGDYPDLHYIQGQSWESQGLPDRAYQSYQHAVDTSSAPAPRRAYVSEQGMDSFRPLHRMGVISQQLGKQEEAARLFHRSLQHHSLYLPALQGIASAFQQLKVPDEDIAGLLIQLAGTGQSAARAAIISTLYELGAYKAIAEQPPELFPLEADTVLLILSSWISTGKYHAFSKTAAKLRAQSLQLSPGGLNTETMRQLWLLEAVCTWELGEALQQEKWLQSPAELRSGLLFIDTQLSSEAVLPQAAVADSVHSPLIHEVIRLAVKLELVTLGKQLVDRFPAHTGDLAEVLYEEGWRAEAGELFIRLVSSKEARGSTLRYLGEMLADKGHYAEAAGWYRLSLEDSPGNEAVLAGLSLCYLHLAEQGLGEVANSFKGEHAHGPLQEDRAAIAHSITVLNRTPWHTVWNYKQRQRGADLSL
>NZ_CP009285.1|WP_099052568.1|6904466_6905384_+|hypothetical-protein
MSSAGTVTNILAGTITSVLGATITAGTLSSAGTITNILEGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSAGTVTNILAGTITSVLGATITAGTLSSVTSISQRSFIELATTGIATSDTYTPLPANTTSVLGTYSYFIVNTGANPINTRVEISADGTNYFVDTTGDNPLPAGSVDVIVPARFLKYTRLSYQSSTPGAASTLNVIFDAQGT
>NZ_CP009285.1|WP_042217351.1|6902440_6902977_-|hypothetical-protein
MPNDAVFNQNSQPLYTEQVNTYIAPGIDTLPEAGAAMSGLLFGYSFASTVTTAAPLVMQVSNPGGSGRTVYISRVIASTGTAAVTLTLLRNATVGGSIVTPVNYNFGSAVTSVTTARTATAAPTGSPATIMSLLLATGPVILDLDGRIILPPGNSLTINITIASGSTAATGNISWWEN
>NZ_CP009285.1|WP_042217350.1|6901837_6902416_-|hypothetical-protein
MPNNYVINDNDQPVYVEMTNTFRAPDISAPPEISASQSAVLFSANASNSATIVLGLASAIITVRINNPAGSGRTLYLSRVSGSIGGTSLLTSISGTFTIVRGGTITSPATVTPVNNNLASSAASAMTVQSSTAAITGGSVLATYQLAPGVFTPAFTGSIIVPPNNALSINVTSSSAAVGTIISALSLTWWER
>NZ_CP009285.1|WP_081972236.1|6901056_6901725_-|alpha/beta-fold-hydrolase
MMDSCLFIHGFTGGEYEIAPLSQILGAHDCLSRTFTLQGHGGSRSDLLQSDRQGWRQSAEDELNTLLTRSEGVHLIGFSTGALIASHLSVQYRARIKSLTLLSTPVFPLNPVQILRTLGQPAMIRNYIRKWGSTPAKATREFQRLVRESFEIYPQMDLPTLIVQGKRDHLVKFKSAGYLEQTIPSGRKQVLIMEKSGHMVCHSEESPAMMNEVLQFIRSSGN
>NZ_CP009285.1|WP_042217348.1|6899806_6900823_+|LacI-family-DNA-binding-transcriptional-regulator
MKVTIKDIAQAAGVAKSTVSKVMNDSPKISEETKTRVRDIIKQMNYTPSSIATGLARQSSNTVAILIDMSKESEFLNQFFYNIIGGVESIIGPLKYELTIANIQHDHAEGHFLHRLVLNKRVDGIIANTSVLTPELCAELNRLEFPYISIGEINPPGTWVDCDNELGGTVLTKHLLEQGYSSVAFIGGEQNEPLFLRRIAGYTATLRQAGLPVRSDRIINGRAAEEDGYAAAMQLLQNPEPPDAIVCMSNFSAFGVLQAARELKIQIPEQLGIATFDEYPLSPYTTPPLTSLNMDTFQLGASAGRLLMDKLGTTATPVSGQLLEPVLIPRLSSLRSRK
>NZ_CP009285.1|WP_042217347.1|6897985_6899686_-|alpha-amylase-N-terminal-ig-like-domain-containing-protein
MPKRLFLYHTAEDPFAYPVGSGTLKLRLFVQSGQSLSCTVVHSDRYDSPGSELPQEMERIGSAGAYDIHEAVLRTGTGKCRYQFHIKNPAGEYVWYGERGMSENREQAGAFQYAYIHRPQATLLPSWSTEAVVYQIYPSSYNKGTLQGIADKISYLHNLGVTAIYMTPIFESPSEHKYNTSDYYRVDPGFGTLEDLKMLVDTAHRHGMKVLLDAVFNHAGDTFFAFKDVLERGEASPYKDWFYIHSYPVSKAPVPGYETFAKAEASMPKLNMDHPEVADYMMEVAKYWVREAGIDGWRLDVANEVTPAFWPRFRRELKAEFPELLLIGEIMHASGPWLRGDQFDGGMNYVLRDAVLEFFAAQSAGPVRFMEQLLHQEALYNDQANSAMFQLLGSHDTLRFLTACKLGGRGWDREATSLSRMKLAVFFQMTYIGLPMIYYGDEVGMEGATDPHCRQPMVWEAQEQNISLQEWYKQLISLRKEHEVLRTGGFRPWFTDEPRNVLGYVRRSEQDRMGLIINNSPNAYQLELCNYRSDKNVLTDLLSGLTIRADKRVLVEIEPFGCLMLH
>NZ_CP009285.1|WP_042217346.1|6896843_6897959_+|M23-family-metallopeptidase
MPALFRSCNTRRTLLCMSAAALLWGSSPAVSVQAARYYKLPELTTTTNSPTAKDSKETAAAARKGLYEQMSAATGIPWFRFAAIDQYERSVAKKKKSPAPSEADSAEAPARLTGISIPAPVWSGPLNPDQEDKFPESITLFGGFGRDGTGDGIADPGNDVDVLYSMAEHLLKYGRSASDFSIGVWEYYHNGRAAQRVAQFAKLYEHFGRLDLSGSAFPLPIGTNYAYRSTWGTGRSWGGARIHEGTDLFAPHGLTVRSTCFGVVETKGWNRYGGWRIGIRDIENRYHYYAHLMGYEKSLSRGDIVIPGQTIGWVGSSGYGSPGTQGKFPPHLHYGIYRDRGITEWAFDPYPLLKQWENQEYRQLKKNKNKK
>NZ_CP009285.1|WP_042220049.1|6913165_6913888_-|glycosyltransferase
MHEPLRKASGNRLTAMMQVRNETGRYLEQVLEELSGFVDDIVIVDDGSTDGTVRLCNSFAKVSKLVTLEHSIFGREWELRKTLWDLAVSTGPDWLLSVDADEFYEDRAKQEMRRLIDQDAYDWVAFRLYDFWGGTTHYREDEHWNIHTKHTRTLVRYLPSFYYFTPRMDHHVPRLPLSYAVLPGFLAELRVKHYGWALEPEELRRKYDRYMELDPEGKWGSLEQYRSILDVDPRLVEWRE
>NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein
MNYIVLSRVSWEDYEYKRLLELLPDRGEVCFAGRMTPVQQRSSGIRSVTLAEIYSLNAGDYTLLVSSPYWLPDVLALQPAYTVALLELCPEGEDSVLWDKYSALLAAKADLAGTTSERIYLEQNLRRKGIVYLSGDQPLSYGLLRREEQLFFLSDYEAIWNRALTELWQPPVDPDGESGWLDIQRRHRTAFYISMCAKMPHQPSVHYLAASYLYLRGDEAASLYLAQSFELMLLHDYTDCLHSHYRFFSAIEAKKGNLELAVRQYEITAFTAEERAKAAQMKQWLSGGEVEHELLRAEILTVNEDGAAANEILSRLTGPEARQRLLLNYIGTFQWLKALQLYHEMEADGTVAAENTGLGGFAGIAGIAGAPEIPGLAGSISPAFEGAVQLPVIEGTLHLLYGRRHDAIRSFLRSAGADQGARQLFAEMADMEEAVQGLRGRAMDGEEHA
>NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein
MSYEAMDAINTIKVMNTVKAVSTERLAGRYSYLEREGLLPLPVQGGVTLVVELRHAQWSAECLRLLLQHSGSSVRLIAVPMTAEFPLQPLSEQFSGEPSLVFLPFAAGNYRVNEALAYAETSFVVLLEDTVMVSPGWLGNLLWPPIDDPVVGVVAPRSSSEWGEGLERLHFAGYSELSAYVAHTLDKRQGEWSYADVLGGACLLMARDVLLRVGGFDSSLVDRRLIIADWCLRARMQGASLALSDPVYVHVLHPLEEGAAENNASNAAASEGEQAYRRKWNLQGSPAAAGPLQIPVDLSGCLPQPSIPLGRHTADTPLVTTVVYFEENWTAADSRERQQTLQEGQSYSNIRWVWVRDSWSQSFPEFPVHERDAVITVHGEKPWLHALENISALYGSEVVVYLSASAAYDSRYIEKLVEILQHSRADIVVSSDFAADEPGQRPETGGITQLLPLERIAHRSGITPGKLMKREGFLRSLALIPDPDLSVGYAGELAGGRDKIQPSAHGGEGHL
>NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase
MTNPIVPGWYADPEARTYHGRHYIYATRSFTEYTRQMNLDAFSSEDLIHWKVHESIIEMDDFPWIWRAVWAPTQIEHNGRYYLVFASNDIQKDGEAGGLEIAVADAPEGPYRGYLHRPLIGEFIHGAQPIDAHLFKDDDGAIYLYYGGWGHCNVCRMNEEMTGFVPFPDGQLIRSVTPPGYVEGPCMIRKDGLYYLMWSMGGWTNGTYRVAYGVSGNPLGPFDNQGTILERQEPVAEGPGHHGYLYLPDRDEWLIVYHRRIIGDPEPGNRMLCIDRMEFAAGGIKPVIMTDRW
>NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein
MAEQQPKLHAWQGVSFTSITINDHFWRPRLEVLRQTTLPDCLSKCEETGRIDNFAKAGGLMEGHYEGKYYNDSDVYKVLEGIAYALMPRRDAALEAEADRIIGLISAAQEADGYLSAYFTLENPQGKWTDMEKHEMYNGGHLIEAAVAYYEATGKRGLLEVACRLADHYDEVFGPGKRHWVEGHQEIELALVKLYRVTQSERYWKLALWLLEERGHGHGAGAIWDNPEWGPAYCQDDVPVREIRQVTGHAVRAMYLYTAMADIVHASGDSAYAEALHRVWAHTVERNMYVTGGIGPSRHNEGFTSDYDLPNETAYCETCAAIAMVFWNHRMNLTFGDGKYADVVEREMYNGALSGISLSGDKYFYVNPLASQGGHHRVPWFETSCCPTNLARFLPSLGQYVYAATEEGLAVNQYLNSEAELVLGSGLGVRLKQSTEYPWDGRIELEVNPASSAGFSIRLRVPEWCRSYRLAAGGVSISGAGALTDQGYLVLNRHWSPGDKVVLELDMPVNLVRANPEVEADRGRVAVQRGPVVYCLEQTDHPGLSYDACSIPAGAKFRVEHLPELLGGVTVLQSRDEAGRPLRFIPYYAWDNRESGFMQVWIREQEERGLYSC
>NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease
MFVIPFVWLIRSSLMNLSQIFTMPPEWIPKPFQWSNFHKALTVLPFDVFFKNTLIIVVTVLVGTVITSSIGAFGFSRIQWKGRDTVFAILMTSMMLPAAVTIIPSFLGWQLMGLYDTLYPLIVPAYFGGGIFNIFLLRQFYLTIPRDFDEAAFVDGANYWQIYTRLIFPLSRSAIIVVALFSFLASWNDFMGPLIYLKSDSLFTLALGLQMFQGTYTAQWDLLMAASATVVLPCVIVFLAGQRYFLEGITLTGLKG
>NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease
MRKGMFYGLLFTAPAILGFAIFTLGPMIASLVLSLTNYNVFKEQTSFAGLDNFVRLFSGEDELFYKSLGITFYFVLLRVPAVILISFGIALLLNLNVKGRAIFRTIIYLPSIVPAVASAMIWMWLLNPDLGLINSLLSRLHLPTSDWLYGEGSVIPSVVLTTLWGIGSTVIIFLAGLSGIPRQYYEAIEVDGGGWFRKLSHVTVPMVTPTIFFNTIMTIIGSFQVFNEAYILTQGGPNNRSLFYVFYLWRTGFRDAEMGYASALAWILFIIILFFTFIVFRTSKSWVYYEGGDRA
>NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein
MLQQKRSVFLTLALVLMLAAVLSACSKSNTASPEASAPSGNAGSKEKITLRMTVWGSPEEVAPYKKAIQNFEAKYTNVKVELQHIAADYDTKLTTMVAGNDVPDIAMMESGTIAFPMAEQGKFYNLQEFLDTDADISPDTLVPNITYSLEPGNVIGIGPGPESFGLFYNEDIFKEAGIEPPPSNVADAWTWDEFVEVAKKLTVDTNDKTAADPDFDPKKIKQYGVNLSTWWGVYSNFIYSNGGDFISADGKTFALNQPEAVEALQKIADLMNVHHVSPSPVQSKNIPATNVALQTKKVAMTVDGQWASAGLAQSKFNFNVGVMPVMKEPVTTVVCGMFSIFKSTKHPQETWELLKALLDPEASIDMLTAGTWMPSPKDWYTDPALLAKWTENLEARPSGYKEAIVDVILTKGHQTPTGYVKNFNNIMDLVNPALDKVWLGQQTAQEAMDSIAVKAQAQIKGRRDIKE
>NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase
MKITFRYRLLASYILLIAVPLLVLGALFYRTSLKIITEQAQKNVYEIVKKNNEVMDTKLRIVDQNSMSLFLDKDLFRIFSQLDPANQVELFAADRQVTAVLGKTFSQNQDIYAYQLWTSYFTFGQTLPQGDPVQSDIYDLARQAGGKLVWIPTYDFVSMFNQPYLQDGNLEFRYLFSATRVLDFTYLSNTKLEKMAAGVERPVLAISFKSEVLKSLYEDSIPGSSRYMVLDPQDKVVASSEPGAVAQTYKEAWLDELQQEKSGARRMTLDGKAVIVCFDRSEVTGWMSVVWIPEAGLVSSFVPVIRASITVMAVVMGIVALILAFFIAGKITKPIKRLLSAMRSVGEGDFQTRVDVVSNDEFGILTQRFNRMNDRIHLLVTENYETKLKEKEAEIQALNMQMHPHFLYNTLNVMNWTAIENDQQELSKMLVCLSNMLHYTSRKTWGAVPLSEEMNWMNNYFYIMSIRFEDKFTVEYDMDPRLFEYDVPRLLFQPFVENAILHGFDQTDSGGIIGIRGWINGRTRHYEVADNGSGMSQATVNAILHQKASSVGIKNTIDRIQMTYGGEYGISIFSSPGKGTKVAITLPL
>NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator
MRILIVDDEPRHLRGMVNLIGRLRPEDQVVAAKDGLSAMELVKAHGPEAILTDIRMPGMDGLEFLERLKVEGIKTRVVMVSAYNLFEYAQKAVRHGAFDYLLKPVEIEKIAEVLSRIDLQLTAEQQQCREEEELQHRLKLASSAYLSRLILSWLNGSAAPEELEELNCYEWLRESGVAVYSELRHRRDSGEQQDSGSFARSLEQAWSEWGEAITVPLSGMMEDGVQAAVTLITLEALTQGKREEARYIAQSLAAEWAHAGQLAHGIGPQCHSLLAGAPQSYLAARTANSYNFYDFRQGLLFADELISTPGAGAPDWGRLYEVLKMDDAALVQEVCAETVYQLADAGQASPMLLKEQASLMLLQIRSDHQDILDKKTGQMLTDTATMLIRSCSSYQELMTKLNHALREAHLALALSRQDKSEVVIAECLGWIQGHTKENLTLERAAEHFHFNPSYFSTLIKSRTGKTFSEHVTAVRMKRAKELLAAEQFRVYEISLECGFQDTKYFCRVFKKYHGMSPKAYKHALSQRKREA

Crispr_ID: NZ_CP009285_20

• CRISPR_ID: NZ_CP009285_20
• CRISPR_location: 6928729-6928804
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_20

Consensus_repeat	Method
AGAGGGATTTATCCCTTTGTTTTCC	CRISPRCasFinder

spacers of NZ_CP009285_20

>20.1|6928754|26|NZ_CP009285|CRISPRCasFinder
TCATGCCGCCCACTTTCGGCGGATTT

CRISPR arrays and Neighbor proteins around NZ_CP009285_20

CRISPR arrays

The CRISPR arrays of NZ_CP009285_20

>merge|NZ_CP009285|20|6928729-6928804|CRISPRCasFinder
AGAGGGATTTATCCCTTTGTTTTCCTCATGCCGCCCACTTTCGGCGGATTTAGAGGGATTTATCCCTTTGATTTCC

>NZ_CP009285|20|18|6928729-6928804|CRISPRCasFinder
AGAGGGATTTATCCCTTTGTTTTCC	TCATGCCGCCCACTTTCGGCGGATTT
AGAGGGATTTATCCCTTTGATTTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_039305346.1|6931585_6932785_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226643
NZ_CP009285.1|WP_042217368.1|6933041_6933596_+|transcriptional-regulator	unknown	unknown	gnl|CDD|224427
NZ_CP009285.1|WP_042217370.1|6942353_6942923_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP009285.1|WP_042220054.1|6929850_6930717_-|glycine-betaine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270357
NZ_CP009285.1|WP_052429690.1|6933696_6938745_-|carbohydrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|185693
NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350148
NZ_CP009285.1|WP_042217369.1|6941147_6942158_-|ketoacyl-ACP-synthase-III	unknown	unknown	gnl|CDD|237245
NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl|CDD|226063
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	unknown	unknown	gnl|CDD|133029
NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009285.1|WP_081972238.1|6927096_6928359_-|sporulation-protein-YunB	unknown	unknown	gnl|CDD|131879
NZ_CP009285.1|WP_081972241.1|6940429_6940945_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP009285.1|WP_042220057.1|6939027_6940044_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP009285.1|WP_039305343.1|6930752_6931589_-|proline/glycine-betaine-ABC-transporter-permease	unknown	unknown	gnl|CDD|226644
NZ_CP009285.1|WP_042220053.1|6928974_6929589_-|VTT-domain-containing-protein	unknown	unknown	gnl|CDD|378149
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042217370.1|6942353_6942923_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.46612e-12
NZ_CP009285.1|WP_042217368.1|6933041_6933596_+|transcriptional-regulator	gnl|CDD|224427	COG1510, COG1510, Predicted transcriptional regulators [Transcription].	2.0978e-39
NZ_CP009285.1|WP_042220054.1|6929850_6930717_-|glycine-betaine-ABC-transporter-substrate-binding-protein	gnl|CDD|270357	cd13639, PBP2_OpuAC_like, Substrate binding domain of Lactococcus lactis ABC-type transporter OpuA and related proteins; the type 2 periplasmic binding protein fold. This subfamily is part of a high affinity multicomponent binding-protein-dependent transport system specific to betaine compounds for osmoregulation. The periplasmic substrate-binding domain, which is often fused to the permease component of the ATP-binding cassette transporter complex, is involved in uptake of osmoprotectants (also termed compatible solutes) such as glycine betaine and proline betaine. Many microorganisms accumulate these compatible solutes in response to high osmolarity to offset the loss of cell water. This 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.	1.12882e-135
NZ_CP009285.1|WP_052429690.1|6933696_6938745_-|carbohydrate-binding-domain-containing-protein	gnl|CDD|185693	cd08023, GH16_laminarinase_like, Laminarinase, member of the glycosyl hydrolase family 16. Laminarinase, also known as glucan endo-1,3-beta-D-glucosidase, is a glycosyl hydrolase family 16 member that hydrolyzes 1,3-beta-D-glucosidic linkages in 1,3-beta-D-glucans such as laminarins, curdlans, paramylons, and pachymans, with very limited action on mixed-link (1,3-1,4-)-beta-D-glucans.	1.62323e-100
NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.13425e-76
NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.39726e-45
NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase	gnl|CDD|350148	cd18827, GH43_XlnD-like, Glycosyl hydrolase family 43 protein such as Aspergillus niger DMS1957 xylanase D (XlnD); includes mostly xylanases. This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have mostly been annotated as xylanases (endo-alpha-L-arabinanase, EC 3.2.1.8). It belongs to the GH43_bXyl-like subgroup of the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. The GH43_bXyl-like subgroup includes enzymes that have been annotated as xylan-digesting beta-xylosidases (EC 3.2.1.37) and xylanases, as well the Bacteroides thetaiotaomicron VPI-5482 alpha-L-arabinofuranosidases (EC 3.2.1.55) (BT3675;BT_3675) and (BT3662;BT_3662). GH43 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. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. 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.	3.63353e-163
NZ_CP009285.1|WP_042217369.1|6941147_6942158_-|ketoacyl-ACP-synthase-III	gnl|CDD|237245	PRK12879, PRK12879, 3-oxoacyl-(acyl carrier protein) synthase III; Reviewed.	0
NZ_CP009285.1|WP_039305346.1|6931585_6932785_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	gnl|CDD|226643	COG4175, ProV, ABC-type proline/glycine betaine transport system, ATPase component [Amino acid transport and metabolism].	0
NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein	gnl|CDD|226063	COG3533, COG3533, Uncharacterized protein conserved in bacteria [Function unknown].	3.84504e-167
NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.748e-12
NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.83169e-50
NZ_CP009285.1|WP_081972238.1|6927096_6928359_-|sporulation-protein-YunB	gnl|CDD|131879	TIGR02832, conserved_hypothetical_protein, sporulation protein YunB. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. Mutation of this sigma E-regulated gene, designated yunB, has been shown to cause a sporulation defect. [Cellular processes, Sporulation and germination].	3.4451e-46
NZ_CP009285.1|WP_081972241.1|6940429_6940945_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	3.71908e-38
NZ_CP009285.1|WP_042220057.1|6939027_6940044_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.40685e-102
NZ_CP009285.1|WP_039305343.1|6930752_6931589_-|proline/glycine-betaine-ABC-transporter-permease	gnl|CDD|226644	COG4176, ProW, ABC-type proline/glycine betaine transport system, permease component [Amino acid transport and metabolism].	1.05838e-125
NZ_CP009285.1|WP_042220053.1|6928974_6929589_-|VTT-domain-containing-protein	gnl|CDD|378149	pfam09335, VTT, VMP1, TMEM41, and TVP38 (VTT) domain. The VTT domain was previously called the SNARE-associated domain, but was renamed as there seems to be no evidence for association with SNARE proteins.	7.0224e-17
NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.05383e-71
NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	8.79265e-81

Protein sequences

>NZ_CP009285.1|WP_081972238.1|6927096_6928359_-|sporulation-protein-YunB
MGRIRKWGNRRAGVPFFGRLRLPRFSWSGLPRPAGRSPAFKAKPSKTVFRPPGSGARFEAKPSRSGSRPTSRGGVFVAKPSRAETRPYRKGAGYETASPGAGAGAPGYRVWRKASRGGGFSLFHGRERKKQEAGAGKGRKPRRRGRFWIILSLLLILAVLQGLRYVEQHLKPPILHLAQIRVKQIATESINKAITSQVADGGNAEALIDWKTDKNGKISGFMLNYKEHMRITSQAAEVIQSTLQELHNQTEHIPLGQALGSPLIASFGPDIPIKIEPQGAVKVELNTRQKNAGINMILVEVFIHIVTEVAVVIPFDMEPQIVDTEIPVSYLMVVGDVPMYYYDNQGQPVGENGSSAPGIAIPAPSLNTEKSGTNADGTLPDGSGSGGNSNSGENNMPAGSGNSAPGANAGNAGANAGSGE
>NZ_CP009285.1|WP_042217364.1|6924872_6926468_-|response-regulator
MRILIVDDEPRHLRGMVNLIGRLRPEDQVVAAKDGLSAMELVKAHGPEAILTDIRMPGMDGLEFLERLKVEGIKTRVVMVSAYNLFEYAQKAVRHGAFDYLLKPVEIEKIAEVLSRIDLQLTAEQQQCREEEELQHRLKLASSAYLSRLILSWLNGSAAPEELEELNCYEWLRESGVAVYSELRHRRDSGEQQDSGSFARSLEQAWSEWGEAITVPLSGMMEDGVQAAVTLITLEALTQGKREEARYIAQSLAAEWAHAGQLAHGIGPQCHSLLAGAPQSYLAARTANSYNFYDFRQGLLFADELISTPGAGAPDWGRLYEVLKMDDAALVQEVCAETVYQLADAGQASPMLLKEQASLMLLQIRSDHQDILDKKTGQMLTDTATMLIRSCSSYQELMTKLNHALREAHLALALSRQDKSEVVIAECLGWIQGHTKENLTLERAAEHFHFNPSYFSTLIKSRTGKTFSEHVTAVRMKRAKELLAAEQFRVYEISLECGFQDTKYFCRVFKKYHGMSPKAYKHALSQRKREA
>NZ_CP009285.1|WP_042217362.1|6923109_6924876_-|sensor-histidine-kinase
MKITFRYRLLASYILLIAVPLLVLGALFYRTSLKIITEQAQKNVYEIVKKNNEVMDTKLRIVDQNSMSLFLDKDLFRIFSQLDPANQVELFAADRQVTAVLGKTFSQNQDIYAYQLWTSYFTFGQTLPQGDPVQSDIYDLARQAGGKLVWIPTYDFVSMFNQPYLQDGNLEFRYLFSATRVLDFTYLSNTKLEKMAAGVERPVLAISFKSEVLKSLYEDSIPGSSRYMVLDPQDKVVASSEPGAVAQTYKEAWLDELQQEKSGARRMTLDGKAVIVCFDRSEVTGWMSVVWIPEAGLVSSFVPVIRASITVMAVVMGIVALILAFFIAGKITKPIKRLLSAMRSVGEGDFQTRVDVVSNDEFGILTQRFNRMNDRIHLLVTENYETKLKEKEAEIQALNMQMHPHFLYNTLNVMNWTAIENDQQELSKMLVCLSNMLHYTSRKTWGAVPLSEEMNWMNNYFYIMSIRFEDKFTVEYDMDPRLFEYDVPRLLFQPFVENAILHGFDQTDSGGIIGIRGWINGRTRHYEVADNGSGMSQATVNAILHQKASSVGIKNTIDRIQMTYGGEYGISIFSSPGKGTKVAITLPL
>NZ_CP009285.1|WP_042217361.1|6921577_6922981_-|sugar-ABC-transporter-substrate-binding-protein
MLQQKRSVFLTLALVLMLAAVLSACSKSNTASPEASAPSGNAGSKEKITLRMTVWGSPEEVAPYKKAIQNFEAKYTNVKVELQHIAADYDTKLTTMVAGNDVPDIAMMESGTIAFPMAEQGKFYNLQEFLDTDADISPDTLVPNITYSLEPGNVIGIGPGPESFGLFYNEDIFKEAGIEPPPSNVADAWTWDEFVEVAKKLTVDTNDKTAADPDFDPKKIKQYGVNLSTWWGVYSNFIYSNGGDFISADGKTFALNQPEAVEALQKIADLMNVHHVSPSPVQSKNIPATNVALQTKKVAMTVDGQWASAGLAQSKFNFNVGVMPVMKEPVTTVVCGMFSIFKSTKHPQETWELLKALLDPEASIDMLTAGTWMPSPKDWYTDPALLAKWTENLEARPSGYKEAIVDVILTKGHQTPTGYVKNFNNIMDLVNPALDKVWLGQQTAQEAMDSIAVKAQAQIKGRRDIKE
>NZ_CP009285.1|WP_042217359.1|6920507_6921395_-|sugar-ABC-transporter-permease
MRKGMFYGLLFTAPAILGFAIFTLGPMIASLVLSLTNYNVFKEQTSFAGLDNFVRLFSGEDELFYKSLGITFYFVLLRVPAVILISFGIALLLNLNVKGRAIFRTIIYLPSIVPAVASAMIWMWLLNPDLGLINSLLSRLHLPTSDWLYGEGSVIPSVVLTTLWGIGSTVIIFLAGLSGIPRQYYEAIEVDGGGWFRKLSHVTVPMVTPTIFFNTIMTIIGSFQVFNEAYILTQGGPNNRSLFYVFYLWRTGFRDAEMGYASALAWILFIIILFFTFIVFRTSKSWVYYEGGDRA
>NZ_CP009285.1|WP_052770361.1|6919680_6920451_-|carbohydrate-ABC-transporter-permease
MFVIPFVWLIRSSLMNLSQIFTMPPEWIPKPFQWSNFHKALTVLPFDVFFKNTLIIVVTVLVGTVITSSIGAFGFSRIQWKGRDTVFAILMTSMMLPAAVTIIPSFLGWQLMGLYDTLYPLIVPAYFGGGIFNIFLLRQFYLTIPRDFDEAAFVDGANYWQIYTRLIFPLSRSAIIVVALFSFLASWNDFMGPLIYLKSDSLFTLALGLQMFQGTYTAQWDLLMAASATVVLPCVIVFLAGQRYFLEGITLTGLKG
>NZ_CP009285.1|WP_042217355.1|6917820_6919662_-|glycoside-hydrolase-family-127-protein
MAEQQPKLHAWQGVSFTSITINDHFWRPRLEVLRQTTLPDCLSKCEETGRIDNFAKAGGLMEGHYEGKYYNDSDVYKVLEGIAYALMPRRDAALEAEADRIIGLISAAQEADGYLSAYFTLENPQGKWTDMEKHEMYNGGHLIEAAVAYYEATGKRGLLEVACRLADHYDEVFGPGKRHWVEGHQEIELALVKLYRVTQSERYWKLALWLLEERGHGHGAGAIWDNPEWGPAYCQDDVPVREIRQVTGHAVRAMYLYTAMADIVHASGDSAYAEALHRVWAHTVERNMYVTGGIGPSRHNEGFTSDYDLPNETAYCETCAAIAMVFWNHRMNLTFGDGKYADVVEREMYNGALSGISLSGDKYFYVNPLASQGGHHRVPWFETSCCPTNLARFLPSLGQYVYAATEEGLAVNQYLNSEAELVLGSGLGVRLKQSTEYPWDGRIELEVNPASSAGFSIRLRVPEWCRSYRLAAGGVSISGAGALTDQGYLVLNRHWSPGDKVVLELDMPVNLVRANPEVEADRGRVAVQRGPVVYCLEQTDHPGLSYDACSIPAGAKFRVEHLPELLGGVTVLQSRDEAGRPLRFIPYYAWDNRESGFMQVWIREQEERGLYSC
>NZ_CP009285.1|WP_042220051.1|6916898_6917780_-|family-43-glycosylhydrolase
MTNPIVPGWYADPEARTYHGRHYIYATRSFTEYTRQMNLDAFSSEDLIHWKVHESIIEMDDFPWIWRAVWAPTQIEHNGRYYLVFASNDIQKDGEAGGLEIAVADAPEGPYRGYLHRPLIGEFIHGAQPIDAHLFKDDDGAIYLYYGGWGHCNVCRMNEEMTGFVPFPDGQLIRSVTPPGYVEGPCMIRKDGLYYLMWSMGGWTNGTYRVAYGVSGNPLGPFDNQGTILERQEPVAEGPGHHGYLYLPDRDEWLIVYHRRIIGDPEPGNRMLCIDRMEFAAGGIKPVIMTDRW
>NZ_CP009285.1|WP_042217354.1|6915226_6916762_-|hypothetical-protein
MSYEAMDAINTIKVMNTVKAVSTERLAGRYSYLEREGLLPLPVQGGVTLVVELRHAQWSAECLRLLLQHSGSSVRLIAVPMTAEFPLQPLSEQFSGEPSLVFLPFAAGNYRVNEALAYAETSFVVLLEDTVMVSPGWLGNLLWPPIDDPVVGVVAPRSSSEWGEGLERLHFAGYSELSAYVAHTLDKRQGEWSYADVLGGACLLMARDVLLRVGGFDSSLVDRRLIIADWCLRARMQGASLALSDPVYVHVLHPLEEGAAENNASNAAASEGEQAYRRKWNLQGSPAAAGPLQIPVDLSGCLPQPSIPLGRHTADTPLVTTVVYFEENWTAADSRERQQTLQEGQSYSNIRWVWVRDSWSQSFPEFPVHERDAVITVHGEKPWLHALENISALYGSEVVVYLSASAAYDSRYIEKLVEILQHSRADIVVSSDFAADEPGQRPETGGITQLLPLERIAHRSGITPGKLMKREGFLRSLALIPDPDLSVGYAGELAGGRDKIQPSAHGGEGHL
>NZ_CP009285.1|WP_042217353.1|6913880_6915230_-|hypothetical-protein
MNYIVLSRVSWEDYEYKRLLELLPDRGEVCFAGRMTPVQQRSSGIRSVTLAEIYSLNAGDYTLLVSSPYWLPDVLALQPAYTVALLELCPEGEDSVLWDKYSALLAAKADLAGTTSERIYLEQNLRRKGIVYLSGDQPLSYGLLRREEQLFFLSDYEAIWNRALTELWQPPVDPDGESGWLDIQRRHRTAFYISMCAKMPHQPSVHYLAASYLYLRGDEAASLYLAQSFELMLLHDYTDCLHSHYRFFSAIEAKKGNLELAVRQYEITAFTAEERAKAAQMKQWLSGGEVEHELLRAEILTVNEDGAAANEILSRLTGPEARQRLLLNYIGTFQWLKALQLYHEMEADGTVAAENTGLGGFAGIAGIAGAPEIPGLAGSISPAFEGAVQLPVIEGTLHLLYGRRHDAIRSFLRSAGADQGARQLFAEMADMEEAVQGLRGRAMDGEEHA
>NZ_CP009285.1|WP_042220053.1|6928974_6929589_-|VTT-domain-containing-protein
MTETINAWIDWLLQSLGLSGPSILFATVPLAVLQSLFGFFPLAILIVLHVSVFNVIGGMIVSWLACNIGAVLVYFLFRRYLFEWFDRKWGYKLKRYDKWQMYLDRYGIWTLVLLRTIPIVPSNIINLMSAVSPIKPAAFIWGTVLGNLSYIWLFGTISSSLIVPREEWNGFLTWYAVFMVILIAIFVRRHWGHLQEDKRKRMGH
>NZ_CP009285.1|WP_042220054.1|6929850_6930717_-|glycine-betaine-ABC-transporter-substrate-binding-protein
MKLSQLGLIMLLMMVVVISGCSSKDNSSVKLAYVAWDSEIASTNVVKEVLESKLGVTVEMLQVDAGPMWAGIADGSADAMVAAWLPGTHASYLEKYGNDVVDAGVNLDGTKTGLAVPAYMDINSIEDLNNPEVAASLDNMIIGIEPGAGIMTSTETAVEAYGLSDYTLLESSSAAMAQELQKAFDNNEPIVVTGWTPHWMFANMDLKYLDDPKNVYGGAEQIHTMVRKGLKDDMPDVYLFLSQFKWTADDMAQVMVKIQGGQSPEEAAKDWVDNNEAKVNEWITGVNL
>NZ_CP009285.1|WP_039305343.1|6930752_6931589_-|proline/glycine-betaine-ABC-transporter-permease
MNLPKIPLGKGVEWLEDWLTTYFGPFFDLIHAVIGGMVSGIDAALTFLPAIVLTILIAALAYWIGKWRMALFAVIGLLLIDNLGLWDPSMQSLALVLTASLLAVIIGVPLGVLCAQSKTFQNIATPILDFMQTMPAFVYLLPAVSFFSLGVVPGVIASIIFAIPPTIRLTNLGIRQVSPELVEAADAFGSTAGQKLFKLQLPIALPTIMAGINQTIMLSLSMVVISSMIGAQGVGAYVYRAVSQAKTGAGFEAGIAIVIIAILLDRLTQKLFKPKQQG
>NZ_CP009285.1|WP_039305346.1|6931585_6932785_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein
MAIIEVKQLTKVFGHDAVRALPLLEQGWSKEKIAREAKLTVGVNKAEFSIEEGEIFVVMGLSGSGKSTLVRLLNRLIEPTGGQVLFKGKDVVQMNPEQLREFRRKNIGMVFQKFALFPHRSVLANAEYGLEVQGVEKSKRTRLAMEALELVGLKGWEHHRPDQLSGGMQQRVGLARGLANDPDILLMDEAFSALDPLIRKDMQQELLELQARVKKTIVFITHDLDEALRIGDRIALMKDGVIVQIGSPEEILIQPANKYVERFVEDVDLSKVLTAAHVMRQPEMIRPERGPRVALQLMRDSGVSSLYVADNEMKLQGVITAENAAQALKENRSILEVMQREIPRVRPDTLLNDLFEMMSETHLPVAVVDEGDKLKGIVIKGAVLSALAGNAVPEGGLGS
>NZ_CP009285.1|WP_042217368.1|6933041_6933596_+|transcriptional-regulator
MNDLEGLLPEQIERISKVRERVIDSIGKNMDLYGITLSIGHLYGYMYFNQGPVTLDELSSTMGMSKTSMSTGVRTLLDLKMIDKVWGKGTRKDLFEVVPDWHQNFSDYFSIKWRKAVEGNMTALNKSLSEIQQMKQDYADEPDIERLLLTDETKIEEAIKYYRWLLKLIEALETGKIFELIPKE
>NZ_CP009285.1|WP_052429690.1|6933696_6938745_-|carbohydrate-binding-domain-containing-protein
MKRNVSAVLAAAVIINGLLSPLGSGAAGAVPAKSKLAAVADATAAVQNGDLAASEMKAFTDVSADNWAAPAVQRWSRSGVISGYGDGSFRPDSQVTRAEFAAIINRIFGYKEAAASLPADIPAGAWYRNDIAKAVAAGYLSAGADNHIQPAAKLKRGEAVVALQKIFRLDTVNHAKGEYSDLAGAGSEVISAADALTAAGYIQGYPGGLFKPDGNITRAELAKMADMLVQELQSSGGEMKLGTVQGNVVLNHEGATLKDSIIEGNLYLTEGIGEGDIRIEGVQVKGTTYIRGGGEHSVTLADSSFGTIQVAKPRGTVRIVASGTTTAGNVQLNSGASLEESNLTGEGFTNVELSAGEKTVTLKGNYGVVSTADPAGSRIALNISGKLAKLVWGAPGTIVLMDKAQVAELLIKPGAKGLAIQGSGSFGTVLNQADDVTVGGSALKQGSRTNLNPAAPQASQLPAAGSGGETAATATPAATPAPEVTPEPTPVITPSPLPTSTPLPEVTPTPAPTSDPWTLVWNDEFDDGSIDPAKWTYDLGDGTIVGNPGWGNNELEYYTSDGKNVKEEDGKLVITARKEAVGGKPYTSSRIKTKGLYSKLYGKFEIRAKAPTGKGLWPAIWMLPEDYTYGNWAASGELDIMEGWGSRPNVVAGTIHYGSQWPDNVYSGKEYVLPGNSTIEDYHTYSIEWEPGEIRWYVDGVLFSTKNDWYSKSSGQPAMNAYPAPFNQRFHLLMNLAVGGNFDGNPTEETVFPSSMEIDYVRIYELTGREYREPVPVEFEKEPYLEGAKLPLEDGNFIHNNGFTEQVEGDAGMGIPNTAHWVLYKDEGADAALSVEPIGGQNFLKVNISSAGGNSYSIQPQAIVSVAKGRYYKLSFDAKTDTARDISVRLTGGAPLGFPSYSPAFKADLTPEIQHFETMFQMKESSDNAARIEFNMGTNASPVWLGNARLEEIDHIPFDHDSAKTPLGSGNHLYNGSFDLGEPDRLSYWHTGATGGAAVLPVVVDPGVLKLEISGGDGGSADVALLQKGIFLVQGHDYKLTFEAESSSPRTAFVELRGNDGTVYASQPVQLTADKQQVEAVFTNLAGATDHLGQFVLRLGGTAGTVYVDNFVLLRTSFYYDPTLTYYPLLNGDFSFGLNNWERLVTEDGGQSTAAAVDGAAKFSITNTGNKAYSVMLFQNGLKAAAGSDYVVEFDASSSVARQISVKAENAKYFSSMDKTIDISPATDHYRFEFRQTTNDTLSLKFLLGKVGDVSVPQSHDIIIDNVKFEIKDAPAKPQELLADSTGNRVSQPIELTFIEKGDWSGKINAVKVDGVTLADELYSLKSGAIIIDAAAFPAEGSYKITVEAEGYVGSSIVQVILANDNNLVVNGSFTSGDSGWSTWSGGGGVSNFKVNEGVAEIEIAAAGGDTWSTQFYQEHIKLEAGKTYELSFKAKSTVARQIIVEYSGTSAQSAQAKFDVTATWATYSAQFSVTNDSPLKLNYLIGKTVGEDGTANGTAHTISLDDIVVREVTGGPVIEPASGTLDNGTFNADQGIKGWTQYFEEPGKGSAAVKDEELDISLNFTGLYNYTAQVDYRDLKLVKGKTYTLTFKARSDVNRLIEVAVEHFGPDYNKYLPVTALALTSEMEVYSYTFTMNDSTDAGAHLVFLMGLIDGNSAQTNTAIQAGNHIYIDDVSLVEAP
>NZ_CP009285.1|WP_042220057.1|6939027_6940044_+|LacI-family-DNA-binding-transcriptional-regulator
MNIKKIAEMAGVSVSTVSKIMNNYSDVSEKTKQRVLEIIEQTGYTPSSSAKTLATKKSNLIGVIFAGELNVEFTHPFFVEVLNSFKKQMGVLGYDLIFFSNEKFISSGDYFSRCLHFHVDGCVIISGQQMEPAIQDLDRSNIPCIGVDLELTGKKSGYVMSDNYQIASKVVEHFYLLGHRELGFIGSTADSDISNRREAGYVKAIAGFGLTMNPKWFVHGDDFFEPSGYAAMKQLIHAGSLPQAIFAASDLLALGAVRALKEHGLRVPEDVAIIGCDDIEACQYTSPTLTTIRQNKERLGVLAAHMLFDLINNQSEGGSFVVEPALIIRESCGSGLNR
>NZ_CP009285.1|WP_081972241.1|6940429_6940945_+|GNAT-family-N-acetyltransferase
MIETKRLIIREMVQSDYDALCGILCDEEVMRAAYESAFNLEEAQNWLNRHLKRYEEYGFGLWAVVLKESNEMIGQCGLTMQGWGEKEILEIGFLFQKAHWHKGYATEAAIACKEYAFSVLNANRVYSIIRDTNIASQKVAVRNGMNIIDKDTKNFRNIDMEFFLYCVERTK
>NZ_CP009285.1|WP_042217369.1|6941147_6942158_-|ketoacyl-ACP-synthase-III
MKGARITAIGSYVPSRRLTNTDLEQMVDTNDEWIVQRTGIRERRISRADEYTSDLCAAAVQDLMKRYGKSVQDVDMVLVATSTPDFSFPSVAAIVQNRLGIPLTSGAIDMSAACAGFVYALHTAHALVSSGLHHKVLVIGADALSKITDYTDRSTSILFGDGAGAVLVESGGDKDHFLGGNLGSDGSGAQHVYRTGLADKVNGVELAATGMLVQNGREVFKWAVRTVPQGVQQVLQNAGAELAEVDWFIPHSANLRMIEPICERLNYPFEQALYSLEYFGNTSAASIPLALDLGIREGKVQNGQRILLYGFGAGLTHAGQLVSLSLDPQVGAPTPY
>NZ_CP009285.1|WP_042217370.1|6942353_6942923_+|TetR/AcrR-family-transcriptional-regulator
MTDKPYHHGNLRNELIEAGIKLINTDGINSFSLRKVAAECKVSHTAPYSHFKNIDELVSAMGEHVTEQFMESLCASVQGQEDSSDAISLLGQAYIDFFMEHPQYFQFLYYHSGIVIDLDNYNSDSYPPFVLFRTTAYQMFQSAGLPEAEFSHQLIALWAMVHGIAALLTNNGVKYSGNWRELLAVQSIL

Crispr_ID: NZ_CP009285_21

• CRISPR_ID: NZ_CP009285_21
• CRISPR_location: 6992742-6992814
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_21

Consensus_repeat	Method
CGGACACCACAGCCCTTAACCAC	CRISPRCasFinder

spacers of NZ_CP009285_21

>21.1|6992765|27|NZ_CP009285|CRISPRCasFinder
TCATAATAAGCCCTTTTGACGGGTTTG

CRISPR arrays and Neighbor proteins around NZ_CP009285_21

CRISPR arrays

The CRISPR arrays of NZ_CP009285_21

>merge|NZ_CP009285|21|6992742-6992814|CRISPRCasFinder
CGGACACCACAGCCCTTAACCACTCATAATAAGCCCTTTTGACGGGTTTGCGGACACCACAGCCCTTATCCAC

>NZ_CP009285|21|19|6992742-6992814|CRISPRCasFinder
CGGACACCACAGCCCTTAACCAC	TCATAATAAGCCCTTTTGACGGGTTTG
CGGACACCACAGCCCTTATCCAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_042217417.1|6997933_6998659_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235914
NZ_CP009285.1|WP_052429693.1|6991714_6992413_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217419.1|6998879_6999224_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_CP009285.1|WP_042217425.1|7002645_7005117_-|alpha-mannosidase	unknown	unknown	gnl|CDD|212101
NZ_CP009285.1|WP_042217424.1|7000460_7001876_+|6-phospho-beta-glucosidase	unknown	unknown	gnl|CDD|182112
NZ_CP009285.1|WP_042217402.1|6983112_6983586_+|DUF2798-domain-containing-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217406.1|6987140_6988022_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_042217401.1|6982114_6982531_-|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP009285.1|WP_042217405.1|6985506_6987126_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270299
NZ_CP009285.1|WP_042217416.1|6994371_6995286_-|phosphotransferase	unknown	unknown	gnl|CDD|270704
NZ_CP009285.1|WP_042220065.1|6984005_6985442_-|glycoside-hydrolase-family-32-protein	unknown	unknown	gnl|CDD|350134
NZ_CP009285.1|WP_042217404.1|6983672_6983936_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042220066.1|6988035_6988974_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP009285.1|WP_167549582.1|6993405_6993984_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217427.1|7005272_7006178_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_CP009285.1|WP_052429694.1|6996530_6997487_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_042217412.1|6992958_6993303_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217408.1|6989427_6990468_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380629
NZ_CP009285.1|WP_042217410.1|6990491_6991472_+|carbohydrate-kinase	unknown	unknown	gnl|CDD|238572
NZ_CP009285.1|WP_042217422.1|6999349_7000321_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_042217417.1|6997933_6998659_-|SDR-family-oxidoreductase	gnl|CDD|235914	PRK07041, PRK07041, SDR family oxidoreductase.	1.28703e-64
NZ_CP009285.1|WP_042217419.1|6998879_6999224_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	1.08107e-35
NZ_CP009285.1|WP_042217427.1|7005272_7006178_+|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	2.29895e-24
NZ_CP009285.1|WP_042217406.1|6987140_6988022_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.44483e-57
NZ_CP009285.1|WP_042217405.1|6985506_6987126_-|extracellular-solute-binding-protein	gnl|CDD|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.56172e-170
NZ_CP009285.1|WP_042217416.1|6994371_6995286_-|phosphotransferase	gnl|CDD|270704	cd05155, APH_ChoK_like_1, Uncharacterized bacterial proteins with similarity to Aminoglycoside 3'-phosphotransferase and Choline kinase. This subfamily is composed of uncharacterized bacterial proteins with similarity to APH and ChoK. Other APH/ChoK-like proteins include ethanolamine kinase (ETNK), macrolide 2'-phosphotransferase (MPH2'), an unusual homoserine kinase, and uncharacterized proteins with similarity to the N-terminal domain of acyl-CoA dehydrogenase 10 (ACAD10). These proteins catalyze the transfer of the gamma-phosphoryl group from ATP (or CTP) to small molecule substrates, such as aminoglycosides, macrolides, choline, ethanolamine, and homoserine. Phosphorylation of the antibiotics, aminoglycosides, and macrolides leads to their inactivation and to bacterial antibiotic resistance. Phosphorylation of choline, ethanolamine, and homoserine serves as precursors to the synthesis of important biological compounds, such as the major phospholipids, phosphatidylcholine and phosphatidylethanolamine and the amino acids, threonine, methionine, and isoleucine. The APH/ChoK-like subfamily is part of a larger superfamily that includes the catalytic domains of other kinases, such as the typical serine/threonine/tyrosine protein kinases (PKs), RIO kinases, actin-fragmin kinase (AFK), and phosphoinositide 3-kinase (PI3K).	7.12657e-56
NZ_CP009285.1|WP_042220065.1|6984005_6985442_-|glycoside-hydrolase-family-32-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, 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.	2.79206e-163
NZ_CP009285.1|WP_052429694.1|6996530_6997487_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.18846e-65
NZ_CP009285.1|WP_042220066.1|6988035_6988974_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	4.48474e-126
NZ_CP009285.1|WP_042217424.1|7000460_7001876_+|6-phospho-beta-glucosidase	gnl|CDD|182112	PRK09852, PRK09852, cryptic 6-phospho-beta-glucosidase; Provisional.	0
NZ_CP009285.1|WP_042217425.1|7002645_7005117_-|alpha-mannosidase	gnl|CDD|212101	cd10789, GH38N_AMII_ER_cytosolic, N-terminal catalytic domain of endoplasmic reticulum(ER)/cytosolic class II alpha-mannosidases; glycoside hydrolase family 38 (GH38). The subfamily is represented by Saccharomyces cerevisiae vacuolar alpha-mannosidase Ams1, rat ER/cytosolic alpha-mannosidase Man2C1, and similar proteins. Members in this family share high sequence similarity. None of them have any classical signal sequence or membrane spanning domains, which are typical of sorting or targeting signals. Ams1 functions as a second resident vacuolar hydrolase in S. cerevisiae. It aids in recycling macromolecular components of the cell through hydrolysis of terminal, non-reducing alpha-d-mannose residues. Ams1 utilizes both the cytoplasm to vacuole targeting (Cvt, nutrient-rich conditions) and autophagic (starvation conditions) pathways for biosynthetic delivery to the vacuole. Man2C1is involved in oligosaccharide catabolism in both the ER and cytosol. It can catalyze the cobalt-dependent cleavage of alpha 1,2-, alpha 1,3-, and alpha 1,6-linked mannose residues. Members in this family are retaining glycosyl hydrolases of family GH38 that employs a two-step mechanism involving the formation of a covalent glycosyl-enzyme complex. Two carboxylic acids positioned within the active site act in concert: one as a catalytic nucleophile and the other as a general acid/base catalyst.	1.50478e-94
NZ_CP009285.1|WP_042217401.1|6982114_6982531_-|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	2.06365e-08
NZ_CP009285.1|WP_042217408.1|6989427_6990468_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380629	cd19974, PBP1_LacI-like, ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. This group includes the ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. 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 sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. 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.	7.11631e-95
NZ_CP009285.1|WP_042217410.1|6990491_6991472_+|carbohydrate-kinase	gnl|CDD|238572	cd01167, bac_FRK, Fructokinases (FRKs) mainly from bacteria and plants are enzymes with high specificity for fructose, as are all FRKs, but they catalyzes the conversion of fructose to fructose-6-phosphate, which is an entry point into glycolysis via conversion into glucose-6-phosphate. This is in contrast to FRKs [or ketohexokinases (KHKs)] from mammalia and halophilic archaebacteria, which phosphorylate fructose to fructose-1-phosphate.	2.13984e-101
NZ_CP009285.1|WP_042217422.1|6999349_7000321_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.34143e-88

Protein sequences

>NZ_CP009285.1|WP_052429693.1|6991714_6992413_+|hypothetical-protein
MNTKQEFDNLMAFANDLINENLGFYYDINYGYFQPETHPIVDFIRLIGRRIQSQLMLMPALYGEMDQMERIFSDNLFFDEWAEVTLDGKSFHFLMRQIDNSSRIIHLARDLVFPSPWIPRKLRDSLIRIGEGTLNGSWRQDIGHEVTLWLPLGISFVEGSGHHSVTAGIIKGEGELYPTSVYDISPIYDHVYTDGKYYYRTHDHSVISEVHFAECAAIFEIGRIMAAQKIIF
>NZ_CP009285.1|WP_042217410.1|6990491_6991472_+|carbohydrate-kinase
MKPYGTVLCVGELLIDFFCTDVDVSLTEGRHFSKQAGGAPANVSAAIARLGGQSAFLGKVGADPFGLFLKQTLEEQKVDTSMLLLDAAAPTTLAFVSLAASGERDFVFNRGADRLLSLEELDRSAIRKAAMLHFGSATALLADPFREVYLTLMDEAKANGQFISFDPNYRGDLWNGRQEEFIALSRAGISKADLVKVSDEELQIISGEADRDAALDLLHAWGAGAVAVTLGKDGTLVSSPASRVLIPSITVKSIDSTGAGDAFVGALLCEISQLAQPAEFMQSAELQQAFVAFANQVGAIVCTKVGAIAALPTQGEVQEFVRQAAL
>NZ_CP009285.1|WP_042217408.1|6989427_6990468_+|LacI-family-DNA-binding-transcriptional-regulator
MKKAKVTIQDIADALGISRNTASKALNGAESIPPETREKVINKAVELKYKQFSYMEAAGSASENQGNIALLTSNLPNSSHFGSQLLSGLEKSISTEGYTLSIYFVRENDINGMTLPGNFEPASVDGIICIEMFSKEYSQLITGLGIPTIFIDCAADIVYPELKADLLLMENEHSVYSMTRKLMDQGLQSFGFVGDYNHCRSFNERWTGFNRALSAAGIPLNPESCIVGRDRDYLLEADWMDRQLDALGEWPSAFICANDFIAIRVMKSLKNRGVMVPEQIAVCGFDDASESRIIEPHLTTVHIYSSHMGNVSAEMLLSRIKEPAKPYQVTHVATDVVFRDSTPVPN
>NZ_CP009285.1|WP_042220066.1|6988035_6988974_-|sugar-ABC-transporter-permease
MIQQRGTEIKKRSQWLGYMRRNYILYLFLAPAVILTIIFKYVPMYGAIIAFKNFSPRKGIMGSEWVGFEHFQRFLSSPNFYDILMNTLKLSAYGLILGFPVPILLALMLNLIRGAKIKKNIQLIVYAPNFISVVVVTGMLFVFLSPAGVVNALITSFTGKPVSFMSDPAYFRTVYILSGIWQTAGWSSIIYVATLANVDPQLHDAATIDGASLLKRIRHIDLPALKPVMAVLFILAAGGIMSIGYEKAFLMQTALNTPTSEIIATYVYKVGLQAGDYAYSTAIGLFNSVINVILLVFVNTVVKRLNEGEGLY
>NZ_CP009285.1|WP_042217406.1|6987140_6988022_-|carbohydrate-ABC-transporter-permease
MDIQYSGKDRMLLVVTYILLGLFILVILFPLVYVVLASFLTPNVLITKGLAIAPSDWTVTGYVKILSNNAMIRGFFNAVLYSAAFALATVFFSVFAAYPLSIEGLAGKRPVMIFFLITMFFGGGLIPTYLVVKDLGMLNTVWAVILPGAISVFNIILAKTYFQGLPKELFQAASIDGASELGIFFRIVLPLSKPIIFVLALYAFVGQWNSYFDAMIYLEDSRLFPLQLVLRSILIQNQVQPGMIADALAQAELKKLSEMIKYSSIVISSLPLIVMYPFFQKYFEKGAMVGSIK
>NZ_CP009285.1|WP_042217405.1|6985506_6987126_-|extracellular-solute-binding-protein
MKKTLQTLSVLALSASVLAGCGGGGGNSAASEDYKLENVTLPLQEKVTLHFMSQSSALAPADPNEKLIYKRLEEKSGVHIDFTNYTNDSFVEKRNLAVASGDLPDAIIDAAYSDYDLLTLGKDGTIVALEELIEKYMPNLQKVLAAAPEYKSMMTAQDGHIYAFPWIEELGSGKESIHSVNGMPWINVEWLNKLGLAMPTTTEELKNVLVAFKNDDPNGNGQKDEIPLSFVLNNGNEDLNFLFGSFGLGDNGDHTVVTNDGKVVFTANQDGYKEGIKYLNELYQLDLIDEEAFEQDYNTYLAKGQSERYGLYFQWDKANITGFNDKYDLMNPLAGPTGEVNVARTNNFGFDRGRMVITGSNKNLELTAKWIDQLYDPQQSVEDNWGTYGDDTQQNIFEYDETAKMLKHLPLEGAAPVELRQKTSIGGPLAILDEYYGKVTTKPDDAAWRLDLMKEKLVPYMKADNNFPRVFYSLEDQKELTAIETDLFAYVSRKRAEWTKTGKVEEEWKEYQAELSRLGLDKWLEIKQAGYDSYLKNKG
>NZ_CP009285.1|WP_042220065.1|6984005_6985442_-|glycoside-hydrolase-family-32-protein
MERAKYRPILHFTPKQHWLNDPNGLIYFEGEYHLFYQYHPHSSIWGPMHWGHAVSKDLITWEELDIALYPDEHGYAFSGSAVVDWNNTSGLFPEKPGIVAVYTSHLEPTEASPSVQRQSLAYSQDNGRTWIKYAGNPVLTHPSKADFRDPKVFWSEAHGKWVMVLATDQTITFYSSPNLRDWRLESEFGEGAGSHDAVWECPDLFQLPVEGTGDSKWVLLVSIGDNSGQRYGSRTQYFVGEFDGSVFTPEHSDIRWLDYGKDNYAGVSFSGIPAADGRRIFIGWMNNWRYANHIPSQGWRGAMTVPRVLTLHAAEGRTLIRQQPVAELDRYFAETAALPDMLLTPGEHRYLSSKASAMELRLELENNEAEQFGLIIHHTDTEHTELIYSAAEGILALRRDQSGETGFSEIFPDLQSTGRMGSLKNLRILLDACSVEVFANDGLSAITSLVFPGDACTGLTFYSTGGSVQLRGNQSFIR
>NZ_CP009285.1|WP_042217404.1|6983672_6983936_+|hypothetical-protein
MLSRKDGISLLLLVVALVLINWFGRSLDARFWTYFTLFANCILVQGVFITLTNVFKARLNRKASKGLILLSLLTGGRSKPAFRLPVA
>NZ_CP009285.1|WP_042217402.1|6983112_6983586_+|DUF2798-domain-containing-protein
MGSNKKEALIFTSLMCFFMVVFMSFYNVILSNGFNNRLFADVAIGLLPALAVALFFDIVVVSKIAKGLAFKIVKPSAPMIKKVLTISCFMVCGMVILMSLYGTLAHFGFRDNFFRHYFSILGLNFICALPLQLIVVGPLTRFLFTRMFPAPAAAHSA
>NZ_CP009285.1|WP_042217401.1|6982114_6982531_-|winged-helix-turn-helix-transcriptional-regulator
MKEYILGLNLVDLISEKHKVLRDRVNTASGEKLNKTETHILAMLELHAMLSISEISRLISISRQGTQKTINNLLAGGYVDTAIVEGNSRDKHIVLTPRGAEVCRSMLEIKQNIEAEIAARIGKDQVEVLRKLLTEDWL
>NZ_CP009285.1|WP_042217412.1|6992958_6993303_-|hypothetical-protein
MLMDKFVKVSLKIGWDEEMRSRSALEYAESGREEEMRSRSALESAESGREEEMRSRSALESAESGREEEMRSRSALESAGSGREEEMRSRSALESAGSGREEKMRGINGPLLRK
>NZ_CP009285.1|WP_167549582.1|6993405_6993984_-|hypothetical-protein
MAVWTPAAGESRIWEMVGTAEGTLQESAYSLQLKLTRLHNGAEWTVLRVPFSLVRAHGWLVSGLDRTAEQPVWISGNRVRLDEAAGSQTVGWYTGRTALHNPLDREVCLAVSAPGAVRLKLDGRTELDRPGAEDALPVYHRGADGQRIELQLSAGIHELEVEALRGQEPLELYVLTVAPAETEQPGILLQPE
>NZ_CP009285.1|WP_042217416.1|6994371_6995286_-|phosphotransferase
MGGTNVWDAEWEVNEEQARTLIGRQFPQLSSKQVKRLGWGWDNTVFLIGDEYVFRFPRRTFAVGAIRMEGKLLPKLEAYLTIPYPKPLFYGEASDEYPAPFLGYAHVPGDFPIGLTEERRALSAETLAKFLRRLHEFPVQAALKCGVQQDHRNLTDIASRKVKLMGFLSKVVEHLSPEESGVIGAYISSLQKDRVEAVNALLHGDLHFKNMLVNENGIVSGIIDWGDLSVGHPACDLSVAYSFLPPYARGVFFETYGGADEETKLLARLIAVYIPMLILMQAVDDGNEAIAAEAKSNIIRALSD
>NZ_CP009285.1|WP_052429694.1|6996530_6997487_-|sugar-ABC-transporter-permease
MSKLTAESNLAGASLHPVSRRAFSRLVRKFGPAYLMLLVPVCFFAVFSLYPIGWALKYVFYYYDGVMPERFTGMANLHRLMEDQIYWSSLWKQALFSLKILIELPLAFVLALFLYTRLRGRNIFRAMFVMPYILPGSTMALVMYILLNPYNGGLNQLLLLKLHLIDQPIQFLSGGWTAFASGMVMDAWQNFGINMLFFLVGLTSIPKDVYESADMDGATWWKRMRYISIPMMYRILQMILFLSILGTLKSMGPFLVLTNGGPNHATEQTFLYIFHQFFGGEAGSNYGYGATVAVVTALMLVVVSVGYFKLTKRMDYHE
>NZ_CP009285.1|WP_042217417.1|6997933_6998659_-|SDR-family-oxidoreductase
MDYWNLKHKKVVIIGGSTGIGLATAAAAAALGAQVVIAGRSKDKLELAADHIRQSSGGAVETYELDNRDERQLELFFAAVSPFDHLFTPGAAYVRGPLTAERDVAISCFDGKFWPQYFAAKYAAPYLAESGSIVLMSGAFSQRPLDGGASYAACNGAIESLGKALAVELAPVRVNVVSPGTIWREGQEGTPRGDHFKEYETMSLVRRTGYDEEIAHTVLYLMTNPFTTGSTLFPDGGYLLR
>NZ_CP009285.1|WP_042217419.1|6998879_6999224_+|helix-turn-helix-transcriptional-regulator
MNLQEPRLRGVIATLDAIDGKWKPLILFILLKDGTRRFGELRRLIPDVSQGTLTKQLRELEQAKLVERRTFPEVPPKVEYSLTAHGKTLSTILDNMCGWGREHLKVLDGSGERL
>NZ_CP009285.1|WP_042217422.1|6999349_7000321_-|LacI-family-DNA-binding-transcriptional-regulator
MSNLDQIAKLSGFSKATVSRVLNHSPHVSQATRDTIMKIMEELDYVPNGNAISLSKGQTEQIGMVTEGINEVMLPFLNSFVETASQHGYQTIIYTSGGDPAKELQAFEDMRRKRVDALVISTCVNDQALLGTFCKYGPIVSWQRMERPEIQSVAMNQYDGYMLGLEHVIKQGYTRIANAFGRPTSMNTSGRIQAYQDIARKYALPVNPDWSPTGIYSIRQGEQLVRELLLNPGERPNAILCANDLVAAGVLNEARRMGVKVPEELAVVGFDNTELAHTLGITSIYNPIAAQAQNAFLLILSRLKGTEPEQQELEFQLVKRATT
>NZ_CP009285.1|WP_042217424.1|7000460_7001876_+|6-phospho-beta-glucosidase
MSIKFPEGFLWGGAVAANQLEGAYNEDGKGWSTQDVAPQGIKGPITEVPTEDNMKLVGIDFYHRYKEDVKLFAEMGFKVFRTSIAWSRIFPNGDELEPNEQGLQFYDDLFDELHKYGIEPLVTLSHYETPLHLSKQYNGWVNRDLVGFYERYARTVFTRYKNKVKYWLTFNEINSILHEPFMSGGIYTPKEQLSKQDLYQAIHHELVASALAVKIGHEINPQSQIGCMILSMPTYPLTPNPDDVIAAMKSEHMNYFFGDVHARGVYPGYMKRYFRENGIEIHMEPGDAEILKHTVDFISFSYYVSICETGDDNKRNQTEGNLFSGAANPYLKASEWGWQIDPQGLRYVLNMFHDRYQKPLFIVENGLGAKDELITGEDGVPTVNDDYRIGYLNDHLVQVGEAIEDGVDVMGYTSWGCIDLVSASTAQLSKRYGFIYVDRHDDNTGTLERYRKKSFHWYKDVIASNGESLQR
>NZ_CP009285.1|WP_042217425.1|7002645_7005117_-|alpha-mannosidase
MKKKLHLLSNAHLDPVWQWEWEEGAAAAVSTFRAAAEFCEENEGYIFNHNEVILYQWVEEYEPALFKRIERLVQAGKWHIMGGWYLQPDCNMISGESFVRQILLGKAYFRAKFGAEPTTAINFDSFGHTRGLVQILVQAGYDSYIFMRPDEMEGLPAGDFSWEGYNGSRVMAHKIEGGYNSLMGKTRGKIEQWLADHPQQRTGLVLWGVGNHGGGPSRMDLAQIAQLMQEREDVEVVHSTPERYFAELAQQGELPVYAGDLNPRFVGCYTSMIRMKQQHRLLENELYMTEKMLSAAALQGLLAYPAAGLQGAMQDLLTAQFHDILPGTAVQNAEEASLRQISHGLETVARLKARAFFALAAGQPKAALKEYPVLIYNPHPYAVTGVFECEFMLEDQNWNEEFSMPVVYQGENRLPCQPEKEHSNIPLDWRKRVAFTAELAPSSMNRFDCRMEMLPAKLLPQLAEQDGCYRFETAELRVVINARTGLMDEYAAGGRSLLRKGAFAPLVMNDNEDPWRMDTDRFNQLEGAFTLMNAEASALFSGVKQPLPAVRVIEDGEVRTVIEAVLSYGSSSICQTYKLPKQGTEVEIELRVYWNEKDKMLKLSIPTVLAQGDFFGQTAFGVQPLDREGRETAAQKWVSVEDATQNLAVTCINNGIHGGDFRQGELRLSLLRSAGYCAHPIGDRPIMAQDRFLPRMDQGERSYTFWLNGGAQRERRKPVDREALVHNERPYALSFFPSGEGETPAPLLMLEDDSIQLSAFKQEEQGENYILRLFEPTGLGGVTTISLPSLGIRREVSLNGFEIKTFRLRPASGVLEEAPLCES
>NZ_CP009285.1|WP_042217427.1|7005272_7006178_+|helix-turn-helix-domain-containing-protein
MDISRYKSELPPVLNMLCQEIRVQDAVIEWVDIIFEQIGTASKCPPHAHTWFEFNYVLSGQLGTRFDGDEITVREGEFFLIPPGRVHSHTYTRGNPHEGLCFRWRLRHADSGHTGDDTRSLYSHLKSLQEWKPGAFRDTEGFSAMLTHFLKEAAAAEPSELGLQLLLIRLLERLCLLQQTLKGHTGTPAIASEPLVRKVEVYLEDFQGDRLNVGELAASLHMSYGHLSREYKKLTGHTLVGRMNKIRLEKARELLLLPGSNISEVAEQAGFADLSYFSKAFKKSYGQAPQTYRKAHSTSSG

Crispr_ID: NZ_CP009285_22

• CRISPR_ID: NZ_CP009285_22
• CRISPR_location: 7095959-7096181
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009285_22

Consensus_repeat	Method
CTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCGTAAAGACCG	CRISPRCasFinder

spacers of NZ_CP009285_22

>22.1|7096014|113|NZ_CP009285|CRISPRCasFinder
CCTCTGCTAATTCGTCCAGCGTCTCCTCACTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCGTAAAGACCGCCTTTGCCAGTTCGTCAAGTGCCTCTTCG

CRISPR arrays and Neighbor proteins around NZ_CP009285_22

CRISPR arrays

The CRISPR arrays of NZ_CP009285_22

>merge|NZ_CP009285|22|7095959-7096181|CRISPRCasFinder
CTGAGGAACGGGGCCAGGGGCAGCAGCGCTTTCGAGCCTTCTTTTTTAAATATAGCCTCTGCTAATTCGTCCAGCGTCTCCTCACTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCGTAAAGACCGCCTTTGCCAGTTCGTCAAGTGCCTCTTCGCTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCATAAAGACCG

>NZ_CP009285|22|20|7095959-7096181|CRISPRCasFinder
CTGAGGAACGGGGCCAGGGGCAGCAGCGCTTTCGAGCCTTCTTTTTTAAATATAG	CCTCTGCTAATTCGTCCAGCGTCTCCTCACTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCGTAAAGACCGCCTTTGCCAGTTCGTCAAGTGCCTCTTCG
CTTACAAACGGGGCCAGCGGCGGCAGCGCTCTTGAGCCTTCTTTCATAAAGACCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009285.1|WP_052429704.1|7102784_7103693_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|372595
NZ_CP009285.1|WP_042217546.1|7104072_7105104_+|metallophosphoesterase	unknown	unknown	gnl|CDD|277347
NZ_CP009285.1|WP_099052504.1|7086325_7086985_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP009285.1|WP_042217536.1|7096725_7097697_-|EamA-family-transporter	unknown	unknown	gnl|CDD|183067
NZ_CP009285.1|WP_042217531.1|7090116_7090794_-|PspA/IM30-family-protein	unknown	unknown	gnl|CDD|281941
NZ_CP009285.1|WP_081972249.1|7091431_7093285_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_CP009285.1|WP_039307347.1|7088081_7088729_-|cell-wall-active-antibiotics-response-protein	unknown	unknown	gnl|CDD|378309
NZ_CP009285.1|WP_042217526.1|7088924_7089632_-|PspA/IM30-family-protein	unknown	unknown	gnl|CDD|224755
NZ_CP009285.1|WP_042217528.1|7089635_7090112_-|PspC-domain-containing-protein	unknown	unknown	gnl|CDD|377200
NZ_CP009285.1|WP_042217543.1|7101376_7102723_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP009285.1|WP_042217540.1|7098798_7099362_-|transcriptional-regulator	unknown	unknown	gnl|CDD|224427
NZ_CP009285.1|WP_167549607.1|7103707_7104031_+|multidrug-efflux-SMR-transporter	unknown	unknown	gnl|CDD|224987
NZ_CP009285.1|WP_042217538.1|7097701_7098154_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP009285.1|WP_174479835.1|7099560_7100466_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096
NZ_CP009285.1|WP_042217534.1|7090841_7091141_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009285.1|WP_042217523.1|7087000_7088035_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_CP009285.1|WP_042217522.1|7084922_7086257_+|hypothetical-protein	unknown	unknown	gnl|CDD|240540
NZ_CP009285.1|WP_042220086.1|7105207_7106032_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270318
NZ_CP009285.1|WP_042220084.1|7100505_7101342_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009285.1|WP_052429702.1|7093281_7095606_+|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|274746

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009285.1|WP_052429704.1|7102784_7103693_+|HAD-family-hydrolase	gnl|CDD|372595	pfam13419, HAD_2, Haloacid dehalogenase-like hydrolase.	1.17638e-27
NZ_CP009285.1|WP_042217546.1|7104072_7105104_+|metallophosphoesterase	gnl|CDD|277347	cd07402, MPP_GpdQ, Enterobacter aerogenes GpdQ and related proteins, metallophosphatase domain. GpdQ (glycerophosphodiesterase Q, also known as Rv0805 in Mycobacterium tuberculosis) is a binuclear metallophosphoesterase from Enterobacter aerogenes that catalyzes the hydrolysis of mono-, di-, and triester substrates, including some organophosphate pesticides and products of the degradation of nerve agents. The GpdQ homolog, Rv0805, has 2',3'-cyclic nucleotide phosphodiesterase activity. GpdQ and Rv0805 belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	8.23308e-13
NZ_CP009285.1|WP_099052504.1|7086325_7086985_-|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	2.21756e-81
NZ_CP009285.1|WP_042217536.1|7096725_7097697_-|EamA-family-transporter	gnl|CDD|183067	PRK11272, PRK11272, putative DMT superfamily transporter inner membrane protein; Provisional.	7.10273e-75
NZ_CP009285.1|WP_042217531.1|7090116_7090794_-|PspA/IM30-family-protein	gnl|CDD|281941	pfam04012, PspA_IM30, PspA/IM30 family. This family includes PspA a protein that suppresses sigma54-dependent transcription. The PspA protein, a negative regulator of the Escherichia coli phage shock psp operon, is produced when virulence factors are exported through secretins in many Gram-negative pathogenic bacteria and its homolog in plants, VIPP1, plays a critical role in thylakoid biogenesis, essential for photosynthesis. Activation of transcription by the enhancer-dependent bacterial sigma(54) containing RNA polymerase occurs through ATP hydrolysis-driven protein conformational changes enabled by activator proteins that belong to the large AAA(+) mechanochemical protein family. It has been shown that PspA directly and specifically acts upon and binds to the AAA(+) domain of the PspF transcription activator.	3.94005e-18
NZ_CP009285.1|WP_081972249.1|7091431_7093285_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	2.26713e-49
NZ_CP009285.1|WP_039307347.1|7088081_7088729_-|cell-wall-active-antibiotics-response-protein	gnl|CDD|378309	pfam09922, DUF2154, Cell wall-active antibiotics response 4TMS YvqF.	3.81811e-34
NZ_CP009285.1|WP_042217526.1|7088924_7089632_-|PspA/IM30-family-protein	gnl|CDD|224755	COG1842, PspA, Phage shock protein A (IM30), suppresses sigma54-dependent transcription [Transcription / Signal transduction mechanisms].	3.62376e-28
NZ_CP009285.1|WP_042217528.1|7089635_7090112_-|PspC-domain-containing-protein	gnl|CDD|377200	pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.	9.44321e-20
NZ_CP009285.1|WP_042217543.1|7101376_7102723_+|ABC-transporter-substrate-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.22182e-75
NZ_CP009285.1|WP_042217540.1|7098798_7099362_-|transcriptional-regulator	gnl|CDD|224427	COG1510, COG1510, Predicted transcriptional regulators [Transcription].	1.03928e-34
NZ_CP009285.1|WP_167549607.1|7103707_7104031_+|multidrug-efflux-SMR-transporter	gnl|CDD|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	1.87583e-28
NZ_CP009285.1|WP_042217538.1|7097701_7098154_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	4.9812e-31
NZ_CP009285.1|WP_174479835.1|7099560_7100466_+|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	9.5521e-92
NZ_CP009285.1|WP_042220084.1|7100505_7101342_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	9.908e-68
NZ_CP009285.1|WP_042217523.1|7087000_7088035_-|sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.62442e-62
NZ_CP009285.1|WP_042217522.1|7084922_7086257_+|hypothetical-protein	gnl|CDD|240540	cd13135, MATE_like_9, Uncharacterized subfamily of the multidrug and toxic compound extrusion (MATE) proteins. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. A number of family members are involved in the synthesis of peptidoglycan components in bacteria.	2.24907e-54
NZ_CP009285.1|WP_042220086.1|7105207_7106032_-|ABC-transporter-substrate-binding-protein	gnl|CDD|270318	cd13600, PBP2_lipoprotein_like_1, Putative periplasmic-binding component of ABC-type methionine uptake transporter system-like; the type 2 periplasmic binding protein fold. This subgroup shares significant sequence homology with the periplasmic substrate-binding domain of ATP-binding cassette (ABC) transporter involved in uptake of methionine (MetQ). The members of the MetQ-like family include the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum, the membrane-associated lipoprotein-9 GmpC from Staphylococcus aureus, and Toll-like receptor 2-activating lipoprotein IlpA from Vibrio vulnificus. They all function as a receptor for methionine. 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. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	5.42861e-93
NZ_CP009285.1|WP_052429702.1|7093281_7095606_+|S-layer-homology-domain-containing-protein	gnl|CDD|274746	TIGR03721, exospore_TM, BclB C-terminal domain. This domain occurs as the C-terminal region in a number of proteins that have extensive collagen-like triple helix repeat regions. Member domains are predicted by TmHMM to have four or five transmembrane helices. Members are found mostly in the Firmicutes, but also in Acanthamoeba polyphaga mimivirus. Members include spore surface glycoprotein BclB from Bacillus anthracis, a protein of the exosporium. The exosporium is an additional outermost spore layer, lacking in B. subtilis and most other spore formers, consisting of a basal layer and, above it, a nap of fine filaments.	6.96291e-37

Protein sequences

>NZ_CP009285.1|WP_052429702.1|7093281_7095606_+|S-layer-homology-domain-containing-protein
MKKAKTRYIEIAHGSENSKKDIKPALVKTSMAVMVLSQVAAVLPSAGFGGTGIASAAEKKGFNDVSSSSWMYKYVMKIAALGFAEGDTTGNFNPKAPLTHQEAAIMAVRFLGIEDPAAAAASSPLEVSDWASAWVQTAINEGLIKAEEETASGWGTQNASREWLTKLVIRLLDKENEALALASEPLPFNDENQISAWATGYINAASQLKVVQGFEDKTFRPTADVTRAQAAAIFSLAERYAPAQSGTVARGTIVSLTGSQIGVLTEAGQVVNLKIDSTTLIFGTSGASTSDIAVGQPITAIYSNGAASYIEIADITKAEITLPAPKGDTGATGAAGLVGATGATGATGATGTTGATGSAGSSGNQGAIGATGATGSAGPVGDIGATGATGPAGEVGATGATGATGPAGEVGVTGATGATGPAGEDGVTGATGATGPAGEDGVTGATGATGPAGEDGVTGATGATGATGEDGATGATGATGPAGEDGVTGATGATGPAGPVGETGETGSTGATGVTGATGATGPTGATGVTGATGESGVTGATGATGEIGVTGATGATGATGATGATGATGATGVTGVTGATGATGATGAPGASTNAYIPFSSGNPATVTTIVGGLPGTGALIGFGNSVSGVSVSSGTIDLTGASGTNLNYAFSVPSAGTITSLSGYFSTTQALTLVGSTVTITAQLYASTTPNNTFVPVPGTAMTLSPPLTGILAIGSISSGVITGLSIPVTAQTRLLMVYTASAAGLSLMNTVEGYMSGGLNISMPATVPTPP
>NZ_CP009285.1|WP_081972249.1|7091431_7093285_+|glycosyltransferase
MQVSIIILAQHLRLLKSCLASIELFTEAPYELIVINDGGGEEISSYLSLHKKARSFTSKERIGVSAGYNLGASFAAGEYLVFMRDHMIVSEEWLSSLTGCARQHPQAAMIGPVSNDVSGPQRLPVICTEMEQLDHIARSFALSKAGQAKSTTRLLSHLLLMRHDAFDLLGGFDEQFGLECYEDDDLCYRALQAGYSLHIALDCFVRYIQPPPLFPEHPGWYNAQLIANKEKARKKWGIDITNALYEMKRSVTVSLCMIVKNEEATLERCLDSVSGLVDEIIIVDTGSTDRTREIALRYTDKVADFTWVNDFAKARNYAFSLATQEYLLWMDADDILLPADAEKFSTLKSALEWNTDAVSMNYNLAFDEHGNVTSSLTRNRLVKRENGFRWIGIVHEYLEVSGKVHRSDISITHGRVHGNSDRNLNIYESRHASGEIFSSRDLFYFANELREHKQWGKAISFYEMFLQQVDSWIEDRINTCGSLSDCYRELGNEQQAKAKALQSFSYDLPRAENCCRLGSLYMLENDFSKAIFWYKMASELTKPLDNYAILQHACWSWLPHLQLCVCYDRIGQYERASAHNEMAAEHIPFDSKVLANRAYFTGLGVARQTYTLGGTTR
>NZ_CP009285.1|WP_042217534.1|7090841_7091141_-|hypothetical-protein
MQRKGNGLAIVLIAIGAVMLLGILPQLIHGIFGILFPVLLVVLGYYGIKSGHKIIGWVVMFIGIMSLLSKLSWIIGPLLGVALVVWGISVLRGKRSRTY
>NZ_CP009285.1|WP_042217531.1|7090116_7090794_-|PspA/IM30-family-protein
MSVFRRMRDITVANLNERLEQSQDPVKLIDQFLHSTREEIGEAERLYQQYASHTKQLQQQVNQATAMRNKREEQALLALKAGEDHLAKLALQEKIIHEEKLEQYSGLLETSRQSLFELESQLNELKIEYQTVYSKRQFYAARMESLRLQQRMNQRASAYGGGDVPKMFGRLEDKMTDWELEAKSLSDLRRMGQEYAVQAGETVATVLEREMARLKEKLNNDGRKE
>NZ_CP009285.1|WP_042217528.1|7089635_7090112_-|PspC-domain-containing-protein
MTRLYRSTRDRVMTGLAGGLSETLGIDSTLFRILLVVSIPFSGGATILVYLIAAMVIPKEPTQYNPFGPGPGAPGGPYGGPYSGRPEHGHGPQGPQGQQGYGPYGGQPGYNPGYDKAGAYTAPDSGLDAMMKDIEKKALQKEVEELKQKLSKYEKGEV
>NZ_CP009285.1|WP_042217526.1|7088924_7089632_-|PspA/IM30-family-protein
MGVFKRIKDMTKASVNDMLDKVEDPIVMLNQYLRDMEAEIHEAEVTVAKQMANERRMKQRVDEAAKVSGQRAAQAELALKNGQEEVTRKLLEEKIYFDQKYAEYSELHAQAEVQAKELVQQLHDMKDEFYKLRNKRNELVSRAQMAKAKKQMSQISSVHSIESGSASLGFHRMEEKIMQLEAEADVLRAPYSPSATAYAKPVDPEKQLKVEEQLAALKSKLNSAPAAPSLDKKEE
>NZ_CP009285.1|WP_039307347.1|7088081_7088729_-|cell-wall-active-antibiotics-response-protein
MDKRNRLIAIGLIGVGCLMIFGKWIGFFSIVALLFLLLGIYRTTSGKVKQGYKLLGIGAVLLLLDHLLLVLGICLISLGMFFVKSKRMQRKAGFMQKQSFSSRFDWDLSPWVMRSLSAWHVLGEADVDLSLAMAEEQETIMLFQGIFGDVDILMSEDYGVEIEAFVLFGSIESGSHRDTGMLNRLNWKSPNYDSSEHKVKFNISYLMGDLDIRFP
>NZ_CP009285.1|WP_042217523.1|7087000_7088035_-|sensor-histidine-kinase
MGKKSSNMVTRSMGEGALFSLIMLLVITYIMYTYGLLQPFEDWKVGVRTAMTLILLPMAFGIGYGFYQGFRSKRKLELLRATLVAWEKGNLTPVMPDLGHDELGRLGEQLGRIGGKWENQVNTLQRLSTNNAKLAEQARVTAIIEERQRLARELHDAVSQQLFAISMTATAVGRTLEKDFDKAQRQIALIEEMSAVAQSEMRALLLHLRPVYLEGKGLEQGLQELIKELKIKVPIDIVFEMDQGVQLLKGVENHLFRIVQEAISNTLRHAKAEKLEIRLHRRGDTVRLTLRDDGIGFEMDESKQTSYGLSNMQERITEIGGSIQFITAPGKGMRIDITVPVVNE
>NZ_CP009285.1|WP_099052504.1|7086325_7086985_-|response-regulator-transcription-factor
MEMEEAEAIKVLLVDDHEMVRIGLAAVLGTEDGIEVVGEAGSGEEGIRLAQEYNPDVVLMDLVMDGMDGIETTRQLLKLYPDCKVIVLTSYLDDEKMYPVIEAGAFSYLLKTSRASEVADAIRAAARGQSVLESQVASKMMNRFRSNARGESPAYKELTEREMEVLKLLAKGKSNQDIADQLIIGIKTVKFHVTNILAKLGVEDRTQAAIYAYKNGLAE
>NZ_CP009285.1|WP_042217522.1|7084922_7086257_+|hypothetical-protein
MLKKWFHRNSADFRLINDLVVPMLFLQILQLLFQLGDQAIIGRLGVEEFAAVGIASSFIFLITGTIGILCAAFNIIGGRFFGNNEIPKFGQAFNTSMTMSIIIGILFELLLLGTGKWILGTVYDLNFAPATHYLYISGMTMGMNMVLFNFSAYFKNINQAKLLTFSFVAAGIVNIFFDYVLVFGKWGFPALGMSGAAVGSVAGYGASIIVCIYFFRKSSLFSFSLRISRPIAKQLLKLYFPMALQDLIEYTLFAMGIMAIISRMESEFIASYTVVTTLLEIIMIPMYCFASSCMTITAKAYGKQQAGYTKYSYLSLQLMLIFSIPLTLIVISFSYPLIAIITDKAVVISLVEHVLPLALALNLMNGLQMIMRSTLQAIDLEKWVLVYSGVVYAVSLVIIYVCIRKLELTGVYLGFGLSYLLLSLGYVYKLQGREPYAHAKTLSR
>NZ_CP009285.1|WP_042217536.1|7096725_7097697_-|EamA-family-transporter
MREKKKVNPVYVVGIALLCVYLFWGGTYVGMKIAIETMPPFLMAGVRFFAAGAVLYIIARLSGAKRPAGREWRSSAIVGALLLLGGNGVVAWSEQRVSSSIASLIVAAVPVWMMLMGWFGRGGKRPNTGVIAGIVLGLVGIAVLVFQPGKGDTGTATDLIGIITLLAASISWAIGSMYSRSAAMPDSPLMSTAAQMLTGGALLMVFSYFTGDWSRLDISGISMRSYLALGYLIIFGSIIGYTAYIWLLKNADASLVSTYAFVNPVVAVLLGWLLVGEQLTLNTLTAAVIIIAAVVLVTIFRGKPQRAATQAALDIQKQQRSVH
>NZ_CP009285.1|WP_042217538.1|7097701_7098154_-|Lrp/AsnC-family-transcriptional-regulator
MDELDIRILKLLEENGRLSHEEIGKLLHISRPSVHQRVGKLEKSGVIKGYRGIVDWSKLDQKIKVMISVKVVSQGFKEAADQIIRIQIPGVSIIECQRLAGEWCMLLKVRVTSPEELTLLLDEILRIPDIKETSTTFILSTIYEDGLKGV
>NZ_CP009285.1|WP_042217540.1|7098798_7099362_-|transcriptional-regulator
MKQAAFGEDNPHRSPREQLLGPMIDAIAQTMDLYGANYSFGQLYGIMFFEDKPMTLEEMKQVMNMSKSNMSYGVRSLIASRMVTKLEEKRERKELYAAETDFFQAFRNFFTLKLQREIDVMQEAMGTAVPELQALIDAADTPEEERQACLRDLDKLKHAAEYYVWLQQFVSGLAEGTVFGGGLPGRE
>NZ_CP009285.1|WP_174479835.1|7099560_7100466_+|ABC-transporter-permease-subunit
MEWGIGTKMTRSKLISGLKPVLFTLPAMVPFALFWLAPLLYVLYLSFTEWDFMSPEKTFVGLQNYTDLLSNPAFYKALRVTVLFCAGSVLPIILLGLGLALLMNRKLKGSALYQVLLFSPWVTPTVAVSIVWSWIYEPDVGLANTVLGFFGLEPIGWLQDPKWALIGVLLVTIWKSVGWAMIFYLVALRNVPSDLLEAGELDGASAVQKFFRITLPLISPTTLFLFVVQLISALQSYDQINVLTQGGPSGSTRTLLYLYYQSAFESFQIGEASTVAVVLVFLCMLLSVFSFSISKRTTHYQ
>NZ_CP009285.1|WP_042220084.1|7100505_7101342_+|carbohydrate-ABC-transporter-permease
MLTRLSGPARQIFFAVLALLMAFPFYWMVTSALKTNDEIWRSPPTLWPEVPLWGNFAAAWNEAPFARYMGNSIFVAVSIVILQTINSGMMAYALTHMKFRLKGVFAGVILFGYMVPATAVYLPGYLVLSELHLLNSYAGLILSNCVSIFSIFLIRQAFLQVSHELVEAGEVDGASHMRILWTVLVPVTRSSFAVLALITFIDQYNNYFWPMLITKDPSLQLVSAGLRSFFVEGGAYGLKWPLIMAASAFTIAPLLLVFLLAQKTIMQSVNMTAGSSKG
>NZ_CP009285.1|WP_042217543.1|7101376_7102723_+|ABC-transporter-substrate-binding-protein
MNVFKRLSAVSMIAGLSVLTACGGNSASGNVTAADGAATVPAADAAPASSAPVTIEFWYGLGGKLGENMESLIQKFNASQQEVIVKGIVQADYTETEQKLQAAIATGQVPAAVLSSNIDWARKGYFAAMDELIAGQPDFNQADFVQTFLSQGQVDGKQYFLPMYGTTQVMYYRKDAFEKSGIDASQIKTWEDLAAAAKKMTVTEGGKTSFYGWEPMWGSGNMIDAVLSKGGNILSEDGKTVTIDSPEWIETWDFFRQAIHEEKTMRIHSGGQGWEYWYKTIDDVMKGQAAGYTGSSGDQGDLDFSIVSAMEQPGWAGVGEGKPVAQAIMAGIPAKAGDAEQQAAMKWLTYFTNSENTAFWSINTGYISVRQSALEDPAFVTFSETNPQIKIPLQQASHASAPFQDPTGGKINDALTIAADKVQIENIPAAEALKEAQQTAQAALDKLK
>NZ_CP009285.1|WP_052429704.1|7102784_7103693_+|HAD-family-hydrolase
MPTLITPHGEHSISAILFDKDGTLLEFVSLWGSWGECFLAQFTRQLQQHGLEFPVQHLASLLGTVHDASGRIVDYDRNGPLAMGTMNDLYAILSWQGYLLGLSWAESMELVDLCRQEADALMEQSKPVLPLPGLLNFLDECAAEGIPLAVVTADETAAAENHLRWIGIRGYFNAVIGTDQVERGKPFPDMALLACERLGVQPAKAAVIGDTNGDMRMAKAAGTAVAIGITGTAAAGPAAAAATRAVAAAASSATDVNAANAHADTAAGSSRTAATRTVRSLLPDADCLVQSYAELGIGRMVR
>NZ_CP009285.1|WP_167549607.1|7103707_7104031_+|multidrug-efflux-SMR-transporter
MAWVFLTLAIVFELSGTISMKISHGFTRPWPSVLMFLFYGISFTSLNVALTSIRVGVAYAVWSGAGIILISIVGAMFFEERLTFSSLLWVTVIVAGIVGLNISAKGH
>NZ_CP009285.1|WP_042217546.1|7104072_7105104_+|metallophosphoesterase
MNTSGHGGQPPLLTFQIITDTHVTADPAHEYNLNFGRALQDLAVHAQGSSGIMHIGDITDHGFAEEYAEVHRILQLHQASLPEILYTLGNHDVGLGHWESRLAMYTSRMGMPGPYHDHWIGGYHFIFLGTEEGLPTFCNLSDEQLKWLDRKLGEKAAVGPFPGTRVVDDLEIYMQPPVAHELDGQLELELESGAAALTERPIFLFLHQPLKDTVAGSLESQEWYGVTQDKELRSILAKYPQTLLFTGHTHWELEVDNTMHPGNGETATMFNAASVAYLWTNADEHKTGSQGFYVEVYADKVLIRGRDFTTGSWIEAAQYEVVNTVSVPGQSSEKSILNNQASL
>NZ_CP009285.1|WP_042220086.1|7105207_7106032_-|ABC-transporter-substrate-binding-protein
MKATFGLTLLALALALAGCGNNKEAEETPAAASTEPVKIKVASLIPPMTDILDIVKPILKEEGVDMEVVVLSDNVQPNEALANKEVDANFFQHVPYMEQFNASKDAKLVAVQPVYDAIYGGYSKRYKSIDELPEGATLVMANDPSNIGRSLQMFADAGLITLKDGVGIQATQADITANTKNFKFEEVDLLMLARMLDDADLVAMTPAYASPLGLTPKKDALITEGEDSAFTITLVAREDNKDSEAIQKLAKAISGPEVKKFLEDNYADIALPAF

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP009285_21	21.1|6992765|27|NZ_CP009285|CRISPRCasFinder	6992765-6992791	27	NZ_CP009285.1	7276088-7276114	1	0.963

1. spacer 21.1|6992765|27|NZ_CP009285|CRISPRCasFinder matches to position: 7276088-7276114, mismatch: 1, identity: 0.963

tcataataagcccttttgacgggtttg	CRISPR spacer
tcataataggcccttttgacgggtttg	Protospacer
********.******************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	63148-63171	0	1.0
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	63136-63159	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	63142-63165	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	5710-5733	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	648039-648062	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	161473-161496	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	161479-161502	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN582103	Podoviridae sp. cty5g4, complete genome	13343-13366	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1335994-1336017	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1336000-1336023	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	390025-390048	1	0.958
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	63154-63177	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	5704-5727	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	648033-648056	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	161467-161490	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN582103	Podoviridae sp. cty5g4, complete genome	13349-13372	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693660	Marine virus AFVG_250M778, complete genome	33354-33377	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693660	Marine virus AFVG_250M778, complete genome	33360-33383	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693660	Marine virus AFVG_250M778, complete genome	33366-33389	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP029249	Salmonella enterica subsp. enterica serovar Thompson strain HFCDC-SM-846 plasmid p846, complete sequence	66413-66436	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP041172	Salmonella enterica subsp. enterica serovar Thompson strain SH11G0791 plasmid pSH11G0791, complete sequence	144895-144918	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP047139	Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence	532990-533013	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP047139	Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence	532996-533019	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP031079	Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence	102854-102877	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP045549	Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence	60539-60562	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_LC492469	Escherichia coli strain M216 plasmid pM216_mF, complete sequence	77328-77351	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	107007-107030	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP012186	Pseudonocardia sp. EC080619-01 plasmid pBCI1-1, complete sequence	35746-35769	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004934	Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence	92724-92747	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	AX955019	Sequence 1 from Patent WO03093461	16508-16531	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN694123	Marine virus AFVG_250M986, complete genome	33630-33653	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693659	Marine virus AFVG_250M987, complete genome	33635-33658	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693659	Marine virus AFVG_250M987, complete genome	33641-33664	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1263122-1263145	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010990	Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence	148823-148846	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_017791	Deinococcus gobiensis I-0 plasmid P2, complete sequence	197488-197511	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004462	Thermus thermophilus phage IN93, complete genome	6678-6701	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	AB063393	Thermus thermophilus phage IN93 DNA, complete genome	6678-6701	2	0.917
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	63130-63153	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	571901-571924	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	161485-161508	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	390019-390042	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693660	Marine virus AFVG_250M778, complete genome	33348-33371	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP031079	Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence	102848-102871	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010614	Phaeobacter inhibens strain P92 plasmid pP92_d, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010626	Phaeobacter inhibens strain P51 plasmid pP51_c, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010671	Phaeobacter inhibens strain P57 plasmid pP57_c, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010685	Phaeobacter piscinae strain P14 plasmid pP14_d, complete sequence	3742-3765	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010633	Phaeobacter inhibens strain P78 plasmid pP78_d, complete sequence	3754-3777	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010660	Phaeobacter piscinae strain P71 plasmid pP71_d, complete sequence	3740-3763	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP019877	Komagataeibacter nataicola strain RZS01 plasmid pKNA02, complete sequence	5032-5055	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP019877	Komagataeibacter nataicola strain RZS01 plasmid pKNA02, complete sequence	32671-32694	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010605	Phaeobacter inhibens strain P83 plasmid pP83_f, complete sequence	3754-3777	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010744	Phaeobacter inhibens strain P59 plasmid pP59_c, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010622	Phaeobacter inhibens strain P30 isolate M4-3.1A plasmid pP30_e, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010732	Phaeobacter inhibens strain P88 plasmid pP88_g, complete sequence	3754-3777	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010655	Phaeobacter inhibens strain P54 plasmid pP54_e, complete sequence	3741-3764	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010648	Phaeobacter piscinae strain P36 plasmid pP36_e, complete sequence	3741-3764	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010711	Phaeobacter inhibens strain P66 plasmid pP66_f, complete sequence	3754-3777	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010702	Phaeobacter inhibens strain P24 plasmid pP24_f, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010748	Phaeobacter inhibens strain P48 isolate M21-2.3 plasmid pP48_c, complete sequence	3753-3776	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP019311	Phaeobacter inhibens strain DOK1-1 plasmid pDOK1-1-4, complete sequence	39750-39773	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010739	Phaeobacter inhibens strain P72 plasmid pP72_d, complete sequence	3742-3765	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN694123	Marine virus AFVG_250M986, complete genome	33624-33647	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693659	Marine virus AFVG_250M987, complete genome	33623-33646	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN693659	Marine virus AFVG_250M987, complete genome	33629-33652	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP031958	Phaeobacter sp. LSS9 plasmid unnamed2, complete sequence	8734-8757	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_001755	Rhodothermus marinus R-21 plasmid pRM21, complete sequence	2458-2481	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP020372	Candidatus Thiodictyon syntrophicum strain Cad16T plasmid pTs485, complete sequence	304791-304814	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP031955	Phaeobacter inhibens strain 2.10 plasmid unnamed3, complete sequence	68067-68090	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_018422	Phaeobacter inhibens 2.10 plasmid pPGA2_71, complete sequence	67831-67854	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_024970	Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence	35502-35525	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_KJ396772	Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence	35502-35525	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	ASHF01000034	Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence	196043-196066	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP010991	Pseudonocardia sp. EC080625-04 plasmid pFRP1-2, complete sequence	54792-54815	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP017565	Paraburkholderia sprentiae WSM5005 plasmid pl2WSM5005, complete sequence	283116-283139	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	561513-561536	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_013858	Azospirillum sp. B510 plasmid pAB510d, complete sequence	27355-27378	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_013858	Azospirillum sp. B510 plasmid pAB510d, complete sequence	6489-6512	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP000663	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence	289031-289054	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP023550	Rhodobacter sp. CZR27 plasmid unnamed2, complete sequence	70489-70512	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	13576-13599	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP034813	Paracoccus sp. Arc7-R13 plasmid unnamed2, complete sequence	150287-150310	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP054618	Azospirillum oryzae strain KACC 14407 plasmid unnamed4, complete sequence	236062-236085	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP026489	Streptomyces sp. 604F plasmid unnamed, complete sequence	185537-185560	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	297912-297935	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP033873	Caulobacter sp. FWC26 plasmid p1, complete sequence	8159-8182	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP024986	Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence	205557-205580	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP000662	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence	458865-458888	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	376527-376550	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP047137	Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence	509154-509177	3	0.875
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1335988-1336011	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP045549	Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence	60533-60556	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	KU884564	Pseudomonas phage PaMx43, complete genome	35503-35526	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	DQ372923	Bacteriophage mu1/6, complete genome	2645-2668	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NC_007967	Streptomyces phage mu1/6, complete genome	2645-2668	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	274879-274902	4	0.833
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	MN657051	Psychrobacter sp. strain ANT_P19 plasmid pA19P2, complete sequence	2012-2035	4	0.833
NZ_CP009285_14	14.1|5378136|26|NZ_CP009285|CRISPRCasFinder	5378136-5378161	26	NZ_CP012886	Mycobacterium chimaera strain AH16 plasmid unnamed1, complete sequence	317502-317527	4	0.846
NZ_CP009285_19	19.3|6912981|30|NZ_CP009285|CRT	6912981-6913010	30	MK936476	Staphylococcus phage SA46-CL1, complete genome	17110-17139	4	0.867
NZ_CP009285_19	19.3|6912981|30|NZ_CP009285|CRT	6912981-6913010	30	MK764384	Staphylococcus phage SA46-CTH2, complete genome	17111-17140	4	0.867
NZ_CP009285_19	19.3|6912981|30|NZ_CP009285|CRT	6912981-6913010	30	MK903033	Staphylococcus phage SA44-CTH7, complete genome	17112-17141	4	0.867
NZ_CP009285_6	6.1|1656060|24|NZ_CP009285|CRT	1656060-1656083	24	CP006582	Mesorhizobium huakuii 7653R plasmid pMHa, complete sequence	42840-42863	5	0.792
NZ_CP009285_14	14.1|5378136|26|NZ_CP009285|CRISPRCasFinder	5378136-5378161	26	NZ_CP009453	Sphingopyxis sp. 113P3 plasmid unnamed, complete sequence	142792-142817	5	0.808
NZ_CP009285_4	4.34|1519293|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1519293-1519326	34	NZ_CP015026	Klebsiella pneumoniae strain Kpn223 plasmid pKPN-065, complete sequence	160201-160234	6	0.824
NZ_CP009285_5	5.3|1533012|27|NZ_CP009285|CRISPRCasFinder	1533012-1533038	27	NZ_CP021407	Celeribacter manganoxidans strain DY25 plasmid pDY25-C, complete sequence	23752-23778	6	0.778
NZ_CP009285_10	10.1|2997429|26|NZ_CP009285|CRISPRCasFinder	2997429-2997454	26	NZ_CP025805	Sulfitobacter sp. SK012 plasmid unnamed1, complete sequence	164463-164488	6	0.769
NZ_CP009285_19	19.1|6912873|30|NZ_CP009285|CRT	6912873-6912902	30	MK936476	Staphylococcus phage SA46-CL1, complete genome	17110-17139	6	0.8
NZ_CP009285_19	19.1|6912873|30|NZ_CP009285|CRT	6912873-6912902	30	MK764384	Staphylococcus phage SA46-CTH2, complete genome	17111-17140	6	0.8
NZ_CP009285_19	19.1|6912873|30|NZ_CP009285|CRT	6912873-6912902	30	MK903033	Staphylococcus phage SA44-CTH7, complete genome	17112-17141	6	0.8
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MG944220	Mycobacterium phage Ruotula, complete genome	38766-38799	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MK494116	Mycobacterium phage Dulcie, complete genome	37428-37461	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN369760	Mycobacterium phage KyMonks1A, complete genome	37422-37455	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MK359354	Mycobacterium phage PinkPlastic, complete genome	37270-37303	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MH576959	Mycobacterium phage Pita2, complete genome	37993-38026	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN585999	Mycobacterium phage Briton15, complete genome	37878-37911	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MK112540	Mycobacterium phage Froghopper, complete genome	36549-36582	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	NC_042326	Mycobacterium virus KSSJEB, complete genome	37215-37248	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MH576974	Mycobacterium phage Sibs6, complete genome	36334-36367	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MK359299	Mycobacterium phage Petp2012, complete genome	37493-37526	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MG962372	Mycobacterium phage McGuire, complete genome	37319-37352	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN428054	Mycobacterium phage JackSparrow, complete genome	37781-37814	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN813700	Mycobacterium phage Atkinbua, complete genome	37747-37780	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	NC_024136	Mycobacterium phage Seabiscuit, complete genome	37406-37439	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MG812486	Mycobacterium phage Acme, complete genome	37321-37354	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN444869	Mycobacterium phage DreamCatcher, complete genome	38630-38663	7	0.794
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	NC_031041	Mycobacterium phage Papez, complete genome	39626-39659	7	0.794
NZ_CP009285_4	4.6|1517432|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1517432-1517463	32	NZ_LR214986	Mycoplasma cynos strain NCTC10142 plasmid 13	470521-470552	7	0.781
NZ_CP009285_19	19.3|6912981|30|NZ_CP009285|CRT	6912981-6913010	30	NZ_CP031578	Klebsiella pneumoniae strain N4b plasmid p1502320-1	1090-1119	7	0.767
NZ_CP009285_19	19.1|6912873|30|NZ_CP009285|CRT	6912873-6912902	30	NZ_CP031578	Klebsiella pneumoniae strain N4b plasmid p1502320-1	1090-1119	8	0.733
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MN234212	Mycobacterium phage Paphu, complete genome	36755-36788	9	0.735
NZ_CP009285_3	3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1505656-1505689	34	MG962370	Mycobacterium phage Kykar, complete genome	37194-37227	9	0.735
NZ_CP009285_3	3.23|1507153|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1507153-1507185	33	NZ_CP039899	Agrobacterium tumefaciens strain CFBP5877 plasmid pAtCFBP5877a, complete sequence	427088-427120	9	0.727
NZ_CP009285_3	3.23|1507153|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1507153-1507185	33	NZ_CP039890	Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499a, complete sequence	427088-427120	9	0.727
NZ_CP009285_3	3.35|1507954|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1507954-1507986	33	CP011075	Brevibacillus laterosporus strain B9 plasmid unnamed1, complete sequence	335131-335163	9	0.727
NZ_CP009285_4	4.6|1517432|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1517432-1517463	32	NZ_CP023312	Vibrio anguillarum strain VIB12 isolate Sea bass plasmid p292, complete sequence	250608-250639	9	0.719
NZ_CP009285_3	3.7|1506062|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1506062-1506097	36	MN850628	Escherichia phage bob, complete genome	17924-17959	10	0.722
NZ_CP009285_3	3.7|1506062|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1506062-1506097	36	MN850629	Escherichia phage mckay, complete genome	22682-22717	10	0.722
NZ_CP009285_3	3.27|1507420|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1507420-1507454	35	JQ807249	Environmental Halophage eHP-30, partial genome	7786-7820	11	0.686
NZ_CP009285_4	4.2|1517166|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT	1517166-1517201	36	NC_009717	Xanthobacter autotrophicus Py2 plasmid pXAUT01, complete sequence	167019-167054	11	0.694

1. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 0, identity: 1.0

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggcggg	Protospacer
************************

2. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

3. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

4. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggcgcg	Protospacer
********************** *

5. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggcgcg	Protospacer
********************** *

6. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

7. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

8. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN582103 (Podoviridae sp. cty5g4, complete genome) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

9. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

10. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgg	Protospacer
********************* **

11. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 1, identity: 0.958

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggccgg	Protospacer
********************* **

12. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggcgggagcggg	Protospacer
*************** **.*****

13. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
agctggggctggggctggggctgg	Protospacer
.******************** **

14. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
agctggggctggggctggggctgg	Protospacer
.******************** **

15. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggctgg	Protospacer
 ******************** **

16. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN582103 (Podoviridae sp. cty5g4, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctga	Protospacer
********************* *.

17. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693660 (Marine virus AFVG_250M778, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggctgg	Protospacer
 ******************** **

18. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693660 (Marine virus AFVG_250M778, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggtgctgg	Protospacer
****************** ** **

19. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693660 (Marine virus AFVG_250M778, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggtgctggggcagg	Protospacer
************ ********.**

20. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP029249 (Salmonella enterica subsp. enterica serovar Thompson strain HFCDC-SM-846 plasmid p846, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggcagg	Protospacer
 ********************.**

21. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP041172 (Salmonella enterica subsp. enterica serovar Thompson strain SH11G0791 plasmid pSH11G0791, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggcagg	Protospacer
 ********************.**

22. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP047139 (Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggctgt	Protospacer
********************* * 

23. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP047139 (Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctgtggctggggctggggctgg	Protospacer
***** *************** **

24. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP031079 (Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
cgctggggctggggctggggctgg	Protospacer
 ******************** **

25. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP045549 (Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
agctggggctggggctggggctgg	Protospacer
.******************** **

26. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_LC492469 (Escherichia coli strain M216 plasmid pM216_mF, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggcagg	Protospacer
 ********************.**

27. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggccgaggctggggcggg	Protospacer
*********.*.************

28. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP012186 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-1, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctgcggctgcggctggggcggg	Protospacer
***** ***** ************

29. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004934 (Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctgctgctggggctggggcggg	Protospacer
*****  *****************

30. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to AX955019 (Sequence 1 from Patent WO03093461) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
gcctggggctggggctggggctgg	Protospacer
* ******************* **

31. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN694123 (Marine virus AFVG_250M986, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggtgctggggctggggcagg	Protospacer
****** **************.**

32. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693659 (Marine virus AFVG_250M987, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggtgctggggctgg	Protospacer
************ ******** **

33. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693659 (Marine virus AFVG_250M987, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggtgctggggctggggctgg	Protospacer
****** ************** **

34. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggtagg	Protospacer
********************..**

35. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010990 (Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctgcggctgcggctggggcggg	Protospacer
***** ***** ************

36. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_017791 (Deinococcus gobiensis I-0 plasmid P2, complete sequence) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggggtcgg	Protospacer
********************. **

37. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004462 (Thermus thermophilus phage IN93, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgaggcgcg	Protospacer
*****************.**** *

38. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to AB063393 (Thermus thermophilus phage IN93 DNA, complete genome) position: , mismatch: 2, identity: 0.917

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgaggcgcg	Protospacer
*****************.**** *

39. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
cgcaggggctggggctggggctgg	Protospacer
 ** ***************** **

40. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctgcggctggggctggggctgc	Protospacer
***** *************** * 

41. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctggaacgga	Protospacer
******************..***.

42. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggccggggggga	Protospacer
***************.**** **.

43. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693660 (Marine virus AFVG_250M778, complete genome) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggtgctggggctggggctgg	Protospacer
 ***** ************** **

44. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP031079 (Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgggtgcgg	Protospacer
*******************   **

45. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010614 (Phaeobacter inhibens strain P92 plasmid pP92_d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

46. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010626 (Phaeobacter inhibens strain P51 plasmid pP51_c, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

47. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010671 (Phaeobacter inhibens strain P57 plasmid pP57_c, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

48. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010685 (Phaeobacter piscinae strain P14 plasmid pP14_d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

49. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010633 (Phaeobacter inhibens strain P78 plasmid pP78_d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

50. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010660 (Phaeobacter piscinae strain P71 plasmid pP71_d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

51. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP019877 (Komagataeibacter nataicola strain RZS01 plasmid pKNA02, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggctga	Protospacer
 ******************** *.

52. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP019877 (Komagataeibacter nataicola strain RZS01 plasmid pKNA02, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctggggctga	Protospacer
 ******************** *.

53. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010605 (Phaeobacter inhibens strain P83 plasmid pP83_f, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

54. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010744 (Phaeobacter inhibens strain P59 plasmid pP59_c, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

55. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010622 (Phaeobacter inhibens strain P30 isolate M4-3.1A plasmid pP30_e, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

56. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010732 (Phaeobacter inhibens strain P88 plasmid pP88_g, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

57. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010655 (Phaeobacter inhibens strain P54 plasmid pP54_e, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

58. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010648 (Phaeobacter piscinae strain P36 plasmid pP36_e, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

59. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010711 (Phaeobacter inhibens strain P66 plasmid pP66_f, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

60. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010702 (Phaeobacter inhibens strain P24 plasmid pP24_f, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

61. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010748 (Phaeobacter inhibens strain P48 isolate M21-2.3 plasmid pP48_c, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

62. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP019311 (Phaeobacter inhibens strain DOK1-1 plasmid pDOK1-1-4, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

63. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010739 (Phaeobacter inhibens strain P72 plasmid pP72_d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

64. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN694123 (Marine virus AFVG_250M986, complete genome) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggtgctggggctgg	Protospacer
 *********** ******** **

65. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693659 (Marine virus AFVG_250M987, complete genome) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggagctggggctggggctgg	Protospacer
 *****.************** **

66. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN693659 (Marine virus AFVG_250M987, complete genome) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
agctggggctggggctggtgctgg	Protospacer
.***************** ** **

67. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP031958 (Phaeobacter sp. LSS9 plasmid unnamed2, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

68. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_001755 (Rhodothermus marinus R-21 plasmid pRM21, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ttctggggctggggctggggcgag	Protospacer
  ********************.*

69. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP020372 (Candidatus Thiodictyon syntrophicum strain Cad16T plasmid pTs485, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
gcctggggctggggctggggcgcc	Protospacer
* ********************  

70. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP031955 (Phaeobacter inhibens strain 2.10 plasmid unnamed3, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

71. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_018422 (Phaeobacter inhibens 2.10 plasmid pPGA2_71, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
aactggggctggggctggcgcggg	Protospacer
..**************** *****

72. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_024970 (Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgcggctgc	Protospacer
***************** *** * 

73. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_KJ396772 (Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgcggctgc	Protospacer
***************** *** * 

74. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to ASHF01000034 (Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggcgcttgggcggt	Protospacer
************ *** ****** 

75. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP010991 (Pseudonocardia sp. EC080625-04 plasmid pFRP1-2, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggtgctggggctggggctgc	Protospacer
****** ************** * 

76. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP017565 (Paraburkholderia sprentiae WSM5005 plasmid pl2WSM5005, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctgaggcttgggcggg	Protospacer
 **********.**** *******

77. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgatggggctggggcaggggcggg	Protospacer
 * ************ ********

78. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_013858 (Azospirillum sp. B510 plasmid pAB510d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
tgcaggggctggggctggggctgg	Protospacer
 ** ***************** **

79. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_013858 (Azospirillum sp. B510 plasmid pAB510d, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggatggagctggggctggggcgga	Protospacer
** ***.****************.

80. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP000663 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggcgctggcgcggc	Protospacer
************ ***** **** 

81. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP023550 (Rhodobacter sp. CZR27 plasmid unnamed2, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggcgctggcgcggc	Protospacer
************ ***** **** 

82. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
agctggggctggggccggggcgcg	Protospacer
.**************.****** *

83. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP034813 (Paracoccus sp. Arc7-R13 plasmid unnamed2, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
cgcaggggctggggctggggctgg	Protospacer
 ** ***************** **

84. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP054618 (Azospirillum oryzae strain KACC 14407 plasmid unnamed4, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggcaggggctggggctggggcttg	Protospacer
*** *****************  *

85. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP026489 (Streptomyces sp. 604F plasmid unnamed, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggcgcttgggcggt	Protospacer
************ *** ****** 

86. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggcgctggcgcggc	Protospacer
************ ***** **** 

87. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP033873 (Caulobacter sp. FWC26 plasmid p1, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
cgcttgggctggggctgtggcggg	Protospacer
 *** ************ ******

88. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP024986 (Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgcggctgc	Protospacer
***************** *** * 

89. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP000662 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
cgctggggctggcgctggggctgg	Protospacer
 *********** ******** **

90. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
cgctggggccggcgctggggcggg	Protospacer
 ********.** ***********

91. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP047137 (Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence) position: , mismatch: 3, identity: 0.875

ggctggggctggggctggggcggg	CRISPR spacer
ggctgtggctggggctggggctgt	Protospacer
***** *************** * 

92. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgggaaaag	Protospacer
*******************. ..*

93. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP045549 (Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgggtgatg	Protospacer
*******************  . *

94. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to KU884564 (Pseudomonas phage PaMx43, complete genome) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
cgctggggctggggctggggcttt	Protospacer
 ********************   

95. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to DQ372923 (Bacteriophage mu1/6, complete genome) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctgggggccg	Protospacer
 *******************   *

96. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NC_007967 (Streptomyces phage mu1/6, complete genome) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
tgctggggctggggctgggggccg	Protospacer
 *******************   *

97. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
tgatggggctggggctggggcgca	Protospacer
 * ******************* .

98. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to MN657051 (Psychrobacter sp. strain ANT_P19 plasmid pA19P2, complete sequence) position: , mismatch: 4, identity: 0.833

ggctggggctggggctggggcggg	CRISPR spacer
ggctggggctggggctgggcagac	Protospacer
*******************  *. 

99. spacer 14.1|5378136|26|NZ_CP009285|CRISPRCasFinder matches to NZ_CP012886 (Mycobacterium chimaera strain AH16 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.846

gctgcaaaaggaggcttttgggcgaa	CRISPR spacer
tgggcaaatggaggcttttgggcgaa	Protospacer
   ***** *****************

100. spacer 19.3|6912981|30|NZ_CP009285|CRT matches to MK936476 (Staphylococcus phage SA46-CL1, complete genome) position: , mismatch: 4, identity: 0.867

tagttgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
*.*** *********** *********** 

101. spacer 19.3|6912981|30|NZ_CP009285|CRT matches to MK764384 (Staphylococcus phage SA46-CTH2, complete genome) position: , mismatch: 4, identity: 0.867

tagttgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
*.*** *********** *********** 

102. spacer 19.3|6912981|30|NZ_CP009285|CRT matches to MK903033 (Staphylococcus phage SA44-CTH7, complete genome) position: , mismatch: 4, identity: 0.867

tagttgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
*.*** *********** *********** 

103. spacer 6.1|1656060|24|NZ_CP009285|CRT matches to CP006582 (Mesorhizobium huakuii 7653R plasmid pMHa, complete sequence) position: , mismatch: 5, identity: 0.792

ggctggggctggggctggggcggg	CRISPR spacer
ccaaggggctggggctggggcggt	Protospacer
    ******************* 

104. spacer 14.1|5378136|26|NZ_CP009285|CRISPRCasFinder matches to NZ_CP009453 (Sphingopyxis sp. 113P3 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gctgcaaaaggaggcttttgggcgaa	CRISPR spacer
gctgaaagaggaggcttttgggccgc	Protospacer
**** **.*************** . 

105. spacer 4.34|1519293|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015026 (Klebsiella pneumoniae strain Kpn223 plasmid pKPN-065, complete sequence) position: , mismatch: 6, identity: 0.824

cgcgtgcgtgcgaccctgcgcgggc----cgcggatca	CRISPR spacer
cgcgtgcgtgcaaccttgcgcgggcgtagcgcgg----	Protospacer
***********.***.*********    *****    

106. spacer 5.3|1533012|27|NZ_CP009285|CRISPRCasFinder matches to NZ_CP021407 (Celeribacter manganoxidans strain DY25 plasmid pDY25-C, complete sequence) position: , mismatch: 6, identity: 0.778

gtgggttcacaagcgccaaaccgccca	CRISPR spacer
tcatgttcagaagcgccagaccgccca	Protospacer
 .. ***** ********.********

107. spacer 10.1|2997429|26|NZ_CP009285|CRISPRCasFinder matches to NZ_CP025805 (Sulfitobacter sp. SK012 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.769

gcaatgggcaaacgtccgaaattcga	CRISPR spacer
ccaatgggcaaacgtccgaacagata	Protospacer
 *******************     *

108. spacer 19.1|6912873|30|NZ_CP009285|CRT matches to MK936476 (Staphylococcus phage SA46-CL1, complete genome) position: , mismatch: 6, identity: 0.8

cagatgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
..* * *********** *********** 

109. spacer 19.1|6912873|30|NZ_CP009285|CRT matches to MK764384 (Staphylococcus phage SA46-CTH2, complete genome) position: , mismatch: 6, identity: 0.8

cagatgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
..* * *********** *********** 

110. spacer 19.1|6912873|30|NZ_CP009285|CRT matches to MK903033 (Staphylococcus phage SA44-CTH7, complete genome) position: , mismatch: 6, identity: 0.8

cagatgttcagttagttgttcagttagttg	CRISPR spacer
tggttcttcagttagttcttcagttagttc	Protospacer
..* * *********** *********** 

111. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MG944220 (Mycobacterium phage Ruotula, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

112. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MK494116 (Mycobacterium phage Dulcie, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

113. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN369760 (Mycobacterium phage KyMonks1A, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

114. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MK359354 (Mycobacterium phage PinkPlastic, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

115. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MH576959 (Mycobacterium phage Pita2, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

116. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN585999 (Mycobacterium phage Briton15, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

117. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MK112540 (Mycobacterium phage Froghopper, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

118. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NC_042326 (Mycobacterium virus KSSJEB, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

119. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MH576974 (Mycobacterium phage Sibs6, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

120. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MK359299 (Mycobacterium phage Petp2012, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

121. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MG962372 (Mycobacterium phage McGuire, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

122. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN428054 (Mycobacterium phage JackSparrow, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

123. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN813700 (Mycobacterium phage Atkinbua, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

124. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NC_024136 (Mycobacterium phage Seabiscuit, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

125. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MG812486 (Mycobacterium phage Acme, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

126. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN444869 (Mycobacterium phage DreamCatcher, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

127. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NC_031041 (Mycobacterium phage Papez, complete genome) position: , mismatch: 7, identity: 0.794

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatctcctgcaggaacttcttgccgatctcgt	Protospacer
*********************.*** **     *

128. spacer 4.6|1517432|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR214986 (Mycoplasma cynos strain NCTC10142 plasmid 13) position: , mismatch: 7, identity: 0.781

acattattttgataacattgataccgaagaaa	CRISPR spacer
aattctttttgataattttgataccgaagaag	Protospacer
*  *. *********. **************.

129. spacer 19.3|6912981|30|NZ_CP009285|CRT matches to NZ_CP031578 (Klebsiella pneumoniae strain N4b plasmid p1502320-1) position: , mismatch: 7, identity: 0.767

tagttgttcagttagttgttcagttagttg	CRISPR spacer
gcgttgttcagtgagttgttcagttgaacg	Protospacer
  ********** ************.. .*

130. spacer 19.1|6912873|30|NZ_CP009285|CRT matches to NZ_CP031578 (Klebsiella pneumoniae strain N4b plasmid p1502320-1) position: , mismatch: 8, identity: 0.733

cagatgttcagttagttgttcagttagttg	CRISPR spacer
gcgttgttcagtgagttgttcagttgaacg	Protospacer
  * ******** ************.. .*

131. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN234212 (Mycobacterium phage Paphu, complete genome) position: , mismatch: 9, identity: 0.735

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatttcctgcaggaacttcttgcctatctcgt	Protospacer
*****.***************.***  *     *

132. spacer 3.1|1505656|34|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MG962370 (Mycobacterium phage Kykar, complete genome) position: , mismatch: 9, identity: 0.735

cggatctcctgcaggaacttcctgcagaaaaatt	CRISPR spacer
cggatttcctgcaggaacttcttgcctatctcgt	Protospacer
*****.***************.***  *     *

133. spacer 3.23|1507153|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039899 (Agrobacterium tumefaciens strain CFBP5877 plasmid pAtCFBP5877a, complete sequence) position: , mismatch: 9, identity: 0.727

ggtgctgtgcaattgggaggccaggcacttgga	CRISPR spacer
catgctgtgcaattgcgaggcgaggctggtgcc	Protospacer
 .************* ***** ****   **  

134. spacer 3.23|1507153|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039890 (Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499a, complete sequence) position: , mismatch: 9, identity: 0.727

ggtgctgtgcaattgggaggccaggcacttgga	CRISPR spacer
catgctgtgcaattgcgaggcgaggctggtgcc	Protospacer
 .************* ***** ****   **  

135. spacer 3.35|1507954|33|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to CP011075 (Brevibacillus laterosporus strain B9 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

agacaaaccccttggcaatatgcttactgacct	CRISPR spacer
agacaaaccccttggctatatgattgtcaccga	Protospacer
**************** ***** **.... *  

136. spacer 4.6|1517432|32|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023312 (Vibrio anguillarum strain VIB12 isolate Sea bass plasmid p292, complete sequence) position: , mismatch: 9, identity: 0.719

acattattttgataacattgataccgaagaaa	CRISPR spacer
caaaggctttgattacattgatacagaagaag	Protospacer
  *  ..****** ********** ******.

137. spacer 3.7|1506062|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN850628 (Escherichia phage bob, complete genome) position: , mismatch: 10, identity: 0.722

ctggatggcaagcagatcgaaaccaatgtatcccgc	CRISPR spacer
gagtctggcaagcagatcgaagccaatgcatcgacg	Protospacer
  *  ****************.******.***    

138. spacer 3.7|1506062|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to MN850629 (Escherichia phage mckay, complete genome) position: , mismatch: 10, identity: 0.722

ctggatggcaagcagatcgaaaccaatgtatcccgc	CRISPR spacer
gagtctggcaagcagatcgaagccaatgcatcgacg	Protospacer
  *  ****************.******.***    

139. spacer 3.27|1507420|35|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to JQ807249 (Environmental Halophage eHP-30, partial genome) position: , mismatch: 11, identity: 0.686

agctcgtcatacagagtgccgtccggtgcaaggct	CRISPR spacer
tcagcgtcatactgagtgccatccggtgcatccac	Protospacer
    ******** *******.*********    .

140. spacer 4.2|1517166|36|NZ_CP009285|PILER-CR,CRISPRCasFinder,CRT matches to NC_009717 (Xanthobacter autotrophicus Py2 plasmid pXAUT01, complete sequence) position: , mismatch: 11, identity: 0.694

tccaggagaccgcgacctagatcggctgcccgcgcc	CRISPR spacer
cgagccatcccgccaccttgatcggctgcccgcgca	Protospacer
.  .  *  **** **** **************** 

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	399667 : 406835	9	Caulobacter_phage(33.33%)	NA	NA
DBSCAN-SWA_2	761813 : 773776	9	Mollivirus(25.0%)	NA	NA
DBSCAN-SWA_3	2716326 : 2726578	9	Bacillus_phage(83.33%)	NA	NA
DBSCAN-SWA_4	4662117 : 4669634	8	Bacillus_phage(33.33%)	NA	NA
DBSCAN-SWA_5	5329911 : 5337936	9	Staphylococcus_phage(57.14%)	NA	NA
DBSCAN-SWA_6	5399383 : 5440013	50	Paenibacillus_phage(17.65%)	transposase,capsid,tail,terminase	NA
DBSCAN-SWA_7	6566809 : 6571669	6	Enterobacteria_phage(50.0%)	NA	NA
DBSCAN-SWA_8	7334467 : 7387354	59	Bacteriophage(23.53%)	tRNA,plate,holin,tail,portal	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP009285|399667:406835|DBSCAN-SWA
AATGACGTATCCCAAAGATTTAAACTATACAATGCCGGCGGAATGGGCCCGGCATGAACGGACCTTCATCTCCTGGCCGGTGCAGGACTCTATGGTCTATCCAGATAACCATGCGGCGGTAAGTGCAGGTTATGCCGAGATTATTAAGGCGATTGCCGAATTCGAGCCGGTGACCGTGGTGGTTAATCCGGGTGATATGGAGACAGTAGAACAGCTCGGACTTGGAGCTAATGTGACGCTGCTGCCTATCAAGCACAACGATGCCTGGCTGCGCGATAACGGACCGACCTTTGTGGTGAATAATGAAGGCAAGCTGGCCGGTGTGAACTGGAAGTTCAATGCCTGGGGCGGCAAATATTCGCCATGGGACCTTGACGATAAGGTAGCTCCGCAAATTCTGGAGCAGCTGGAGATCAGCAGCTTCGATGCACCGCTTGTCATGGAAGGCGGCTCGATTCATACCGATGGCGAAGGAACACTGCTGACCACCGAAGAATGCCTGCTGAACACGAACCGCAATCCGGAGCTGGACCGGGAAGAGATTGCCGGCTTAGTGAAGCGATATACCGGGACTGAGTCGATCATCTGGCTGAAGCGCGGCCTCAGCGGAGACGAGACGGACGGTCATGTCGATAACATCGCGTGCTTCGCTGCGCCGGGCAAGGTGGTCATCCAGGTCTGCGGGGACCCGGAGGATGAGAATTATGCCATTTCGGAGGAGAACCTGCGTATTCTGGAGCAGGCTGTTGATGCCAAGGGCCGGAAGCTGGAGATTATCCGCATTCAGCAGCCGCCCCGTGTGGATTATGAAGACAGCCGGTTGACCCTGAGCTATCTGAATTTCTATTTCGTGAACGGCGGGATTATCCTGCCGGTATTCGGCGGTACGGCGGCAGAGACAGACAAGCTTGCCGAAGAGACGCTTGCCGGGCTGTTCCAAGGCCGCAGAATCCGCACAGTGAACGGAATGGCTGTAATCGGTGAAGGCGGGAACGTACACTGCACCACCCAGCAGATGCCTGCGGTGAAATCGTAGCTTCAAATAAGGAGGAATAACCGTGAGAAAAGTAAAAGTAGCCGCAACACAAATGAGCTGTTCCGGCGACATTGATGAGAATATCCGCAAGGCCGAGACACTGGTCAGAGAAGCGGCAGCCCAGGGCGCACAGATTATTCTGCTGCAGGAGCTGTTTGAGACACCGTATTTCTGCCAGAAGGAGAAATCCGATTACTACGCCTATGCCACCGAGCTTGAGCACAACAAGGCTGTGAACCATTTCAAGGCGATAGCCAAAGAACTCGAAGTGGTGCTGCCGATCAGCTTTTATGAGAAAAAGAACTACGCGCGTTATAACTCGCTGGCCGTGATTGATGCTGATGGAACGGTGATGGGCAAGTACCGCAAGAGTCATATTCCTGACGGCCCCGGCTATGAAGAGAAGTTCTACTTCAACCCGGGCGATACCGGCTTTAAGGTGTGGAATACCCGGTATGCCAAAATCGGCGTCGGCGTCTGCTGGGATCAGTGGTATCCGGAAGCAGCGCGGGTAATGAGTCTGATGGGTGCGGAGATTCTGTTCTATCCTACAGCTATCGGCTCGGAGCCGCAGGACGGATCGATCGATTCCAAGGATCACTGGCAGACCTGCATGCTGGGCCATGCGGCCGCTAACCTGATTCCTGTCGTGGCCTCCAACCGGATCGGTGAGGAGATTGACGAGGATTCCAGCATTAACTTCTACGGCTCATCGTTCATTGCCGGCCCGCAGGGCAACAAGATTGCCGAAGCCGGACGTGATGAGCAGACGGTACTGGTCAGTGAGTTTGATCTCGATGCGCTTGAAGTTGGCAGGATCGAGTGGGGGATCTTCCGCGACCGCCGTCCGGAGCTGTACCGGCTGATTGCTTCGTATGACGGGGATTTGACATTCTGATTGTAAATGAATGAATTAAATAACAGATTACAATAGTGAGCAGCCAGGACGCTGCCGGGGATATGACTCTCCGGACAGCCTCCTGGCTGCTTTTTATATGAAGATAGACCTGAATTCTAAGATTAGCGGCTGAAAATGTTACAATACTACGATATTATGTCATGTTATATAACATATCGAGGAAAAGTTAATTGTCACCACTGCTTTAATCTGATAAAATCTTTTTAAGTTATTTTATAAATAAGTAGGGGGATTGGAGCATGGGAATCAGAAAAAAATGGGCTATGTCAGGTATGGTGGCATTACTGGTTTTGGCAATGGTCGGCTGTGGTTCGAACAATAACGCAGGCAGCGGCGATGCGGCAGGAGAGAGCATCAAGTTCGCCAGCGATGCCAGTTATGCACCTATGGAGTATATGGATACAGATACTATCAAGGGTTTTGACATTGATTTCATTAAGGCGGTTATGGAAGAAGCGGGTATTGATTACACCGTGACAAATACAGGCTGGGATACGATGCTGACCAGTGTTCAGCAAGGCACTGAATATCAGGCGGGCCTGTCGTCGGTATCCATTACTGATGAGCGTAAAGAAACCTATGACTATTCCATTCCTTACTTCGAATCAACGAACATGATCATGGTCAAGGAAGGCAGCGATATCAAGTCTGCCCTTGATTTGAAGGATAAGAAAGTTGCCGTTCAGGCAGCAACAACTGCGGATGATCTGATGAGCGGCATTATGGGGATCGACAACGGCAATCTGAAGCGCTTTGACAGCAATGCGGTAGCCCTGATGGAGCTGAACGGCGGCGGAGCGGATGCAGTGGTTGCGGATATCGCCATCGTGAACGAATACATTAAGAACAATCCGAATGAGAAGCTGGTCGGTATTATCGACAAGGAGAACTTCGGTTCCGAATATTACGGCATCCTGTATCCTAAGGGCAGCGAATGGAAAGCCAAGCTGGACCCGGCGATCAAGACGATTATCGAGAACGGCAAATATGCGGAGATCTACAAAGAGTGGTTCGGTGAAGAGCCGGACACTAAGACGCTTTTGAGCGCAGAGTAAGCGGAGTAACAATTAAGCATGCGTAATGATTGCTATTGCGCATGCTTCTTTTTTTGAAACACAAGAGAAACATAGAGAAAGCTATAAGCAGAAGAGAAGGGAAGAGTTCTATGGATTTCAGATTTGACATCATCGTACATTATTTACCGGTTTTACTTAAAGGGACTTTGTTCACCATAGGCGTATCGCTGGTATCGATCCTGTGCGGCTCCATTCTGGGACTGGTTATCGGATTCGGCAAAATGGCGCCCAAGTGGTATTTCCGCTGGCCGTTTCATGCCTATATCAACATCTTCCGCGGAACACCGCTGTATGTGCAGATCCTGATCGTCCATTTCGGGCTGATTCCGTTATTCTATGGTAAAACCTATGCGCTGATGAGCGCATTTGTGGCGCTTTCGCTCAATTCCGCGGCGTATTCCGCCGAAATCTTCCGCGCGGGTATCCAGTCGATTGATCCCGGACAACGGGAAGCTGCCCTGTCACTCGGGATGACCAAATTACAGGCGATGCGTTTCATTATTCTGCCTCAGGCGATCAAACGGATGGTTCCGGCGTTCGGGAATGAATTCATCGTCCTCGTTAAGGATTCCTCGCTGCTGGCACTTATTGCCGCACCTGAGATTATGTATTGGAGCAACACCATGAAGGGCCAGTATCTGCGGATCTGGGAGCCTTATTTGACCGCAGCACTGATCTATTTCATCCTGACCTATTCCCTCAGCAAGCTGCTTAATTATATCGAACGGAAGGTGTAACCCTATATGGAGCCTATTATCTCAGTCAAGCATCTGCATAAATCCTTCGGTGCCCATAAGGTACTGTCCGACATCAGCGTCGATATTCACAGCCGGGAGGTTGTGGTGGTGATCGGGCCTTCGGGTTCGGGCAAATCGACCTTTCTGCGCTGCCTCAATCTGCTGGAGCAGCCGCAGGAGGGCGATATTATTATTGAAGGCACTTCCTTGATGGCCAAAAGCACAAGGATTAACGATATCCGTACAGAAGTTGGCATGGTGTTTCAGCAGTTCAATCTGTTTCCGCACAAAAAGGTGATCGAGAACATTATGCTGGCCCCGATGCAGGTCCGCAAATGGCCGGCTGACAAAGCCCGTCAAAAAGCGCTGGAGCTGCTGCAAAAGGTGGGACTGAGCGAGAAGGCGGAGATGTATCCTTCCTCGCTTTCAGGCGGTCAAGCCCAGCGTGTAGCGATTGCGCGCGCTTTGGCGATGGAGCCGAAGATCATGCTGTTTGATGAACCGACTTCTGCACTTGACCCCGAAATGGTGGGCGAGGTGCTGGCAGTGATGAAGGATCTGGCCCGCGAAGGAATGACCATGGTCGTAGTCACGCATGAGATGGGCTTTGCGCGTGAAGTGGGAGACCGCGTCCTCTTTATGGAGCAGGGGATTATTGTGGAGCAGGGTGCGCCCGAACAGTTATTCGGGAATCCGTCACATGAACGTACCCAGGAATTCCTGTCCAAGGTACTGTGAGATTTTGTCAAAGTAGAATATTGTCATTTAATCGGTTATATTAGAAGAGCAAGAATTAGGCATGGAACCATCAGTGAATATCTGCCCGGAACGGCGGGGAGGAGGCTCGGGGATATCTTTTTTTAAAGTATAAGGATTTATGGGCTACGCATAATAATTTATCCTTATATTTCCTGCAGAAGCGGATATGGTGCTTATAGTACGGCACAGCCTTTTCTACTGGTCATAATTCAGAATGATAGAAGGAGAATACGATGAGCACATTTAAAAATTGGCTGAACACTACCAAAACCGGACTGACAGAACAAGTGAAGAAGTTTAAAAATAAAGACTTTATGAACGCGGTAGTTGCGGGCTGCGCACTGGTGGCTGCGGCTGACGGCAAAATTGAGGAATCCGAGAAGAACAAAATGGCCGGATATATGAACCTCAGCAATGAATTGAAGGTATTTGACATGAGAGATGTCATCAACCAGTTCAATTTCTATGTGAGTAACTTCGAATTCTCACCGGAAATCGGCAAGCAGGAAGCACTGAAATCGATCGCGAAATTCAGCAGCAAACCGGAAATCGGACGTGTCATTGTTGGCGTATGCTCTGCGATCGGTGCGGCTGACGGCGACTTCGATGAGCATGAGAAAGCGGTTGTACGGAATATCTGCAGTGTGCTCGGACTTAGCCCAAGCGAATTCAGCCTGTAACAGCGGGCCGGAAGGCATCCGCTAAATTGGATGAAACTTAGGCGTTTTTCCATCGTATCACTGATATAACACTCGCAAGAAGAACTTACAGGCAGTGATTTCTACTGGAAACGGAGGTACGTAAAGTTGGCTGGAATCAATCTCGTAAAAGGTCAGAAGATCGATTTAACCAAAGGGAATGCCGGACTGTCTAACGTTATCGTAGGACTGGGCTGGGACCCTGCCGAACCGGCAAGAGGCTTCTTTGGTGTCAAGAAACAGGCGAATGTAGACTGCGATGCTTCAGCCTTGCTGCTGAATGAGAATGGCAAGCTGACCAATAAGCTGAACCTCGTCTGCTTTCACAACAAACAGAATGCGAACAATTCCGTGGTTCACTCGGGAGATAACCTGACGGGTGAAGGAGACGGGGACGACGAGCAGATTATGGTGAATCTGAAGGCGATTCCTGCCGATGTCCATAAGGTTCTGGTTGTGGTCAACATCTACGACGCCGTGAACCGCAAGCAGGATTTCGGGATGATCAAATCGGCGTACATCCGGATTATTAATGCAGCAGGGAATGGCGAGCTGATCAAGTTTAATCTGACGGACAATTACACAGGCTTCACGGCACTGATCTGCGGCGAGCTCTACCGTCATGGTGAAGAGTGGAAATTCGCAGCTATCGGTGAAGGCGCGCACGCAGCACATATCAATCAACTGGCTGAACGTTATATCTAATTCCAATTTGAGAAAAGAGGGTTCTATTCATGGCTATTAACTTATCCAAGGGACAAAAAATCGATTTGACCAAAACTAATCCGGGCTTGTCCAAAATTACAGTCGGCCTCGGATGGGATACGAATAAATACGATGGCGGTAAGGATTTTGACCTTGACGTGTCTGTATTCCTGACGAATGCTAACGGCAAAGTGGATAAAGAAACGAACTTCATCTTCTTCAACAATAAGCAGAACGAGAACGCTTCCGTTGTTCACACCGGCGACAACCGCACAGGTGAAGGCGACGGAGACGATGAGCAGGTTCAGGTAGATTTGCTCAATGTTCCTGCGGATGTTGATAAAATTGCGTTCACCATTACAATCTATGAAGCAGAATCCAGAAGCCAGAACTTTGGACAAGTCTCCCGTTCTTATGTACGTATCGTGAATGATGCGAACAGTGAAGAATTGATCCGTTTTGACCTGGGGGAAGATTTCTCCGTTGAAACCGGTGTGGTAGTCGGCGAGCTGTACCGCAATGGCGCAGAATGGAAATTCAATGCGATCGGCAGCGGCTACAAAGACGGACTCGCCGGACTGACCCGTGATTACGGTCTGCAATAAGACCCGGCTGACTCCGGGGAATTAAATCTTTGAGGAAAGAAGGTTTTTGCCAGTGACGATCAGTCTTTCCAAAGGACAGCGGATCGATCTTACCAAGACCAATCCGGGCCTGACGAAGGTAGTTGTAGGACTTGGCTGGGATACAAACAAGTATAGCGGCGGCAAGGATTTCGATCTGGATGCATCAGCATTTCTGCTGCATGAGGACGGCAAAGCCAAAGGCGAAGACGACTTTGTATTCTATAACAACCCAAGCGGCGGGACAGGCTCCGTAACCCATACAGGCGATAACCGTACAGGTGAAGGCGACGGGGACGATGAGCAGATTCTCGTAGACTTCAGCCTGGTGCCGGCGAATATTCAGCGCATTGGGATTACAGTGACAATCTACGATTATGAAACTCGTGTGCAGAACTTCGGACAAGTCTCCAACGCGTTTGTACGCGTTGTGGATGCCTCCAGTGACCGTGAGATTCTGCGGTTTGATCTGGGTGAGGATTTCTCCACTGAGACTGCCGTTGTCTTCTGTGAATTCTACCGCCATGGCACGGATTGGAAATTCCAGGCGGTCGGCAGCGGCTTTGCCGGCGGGCTAAGCGCTTTATGTAAGAATTATGGACTGGATGCACAATAA

Protein sequences of DBSCAN-SWA_1

>NZ_CP009285|399667:406835|404999_405596_+|WP_042210162.1|DBSCAN-SWA
MAGINLVKGQKIDLTKGNAGLSNVIVGLGWDPAEPARGFFGVKKQANVDCDASALLLNENGKLTNKLNLVCFHNKQNANNSVVHSGDNLTGEGDGDDEQIMVNLKAIPADVHKVLVVVNIYDAVNRKQDFGMIKSAYIRIINAAGNGELIKFNLTDNYTGFTALICGELYRHGEEWKFAAIGEGAHAAHINQLAERYI
>NZ_CP009285|399667:406835|405625_406201_+|WP_042210163.1|DBSCAN-SWA
MAINLSKGQKIDLTKTNPGLSKITVGLGWDTNKYDGGKDFDLDVSVFLTNANGKVDKETNFIFFNNKQNENASVVHTGDNRTGEGDGDDEQVQVDLLNVPADVDKIAFTITIYEAESRSQNFGQVSRSYVRIVNDANSEELIRFDLGEDFSVETGVVVGELYRNGAEWKFNAIGSGYKDGLAGLTRDYGLQ
>NZ_CP009285|399667:406835|404426_404873_+|WP_042210161.1|DBSCAN-SWA
MSTFKNWLNTTKTGLTEQVKKFKNKDFMNAVVAGCALVAAADGKIEESEKNKMAGYMNLSNELKVFDMRDVINQFNFYVSNFEFSPEIGKQEALKSIAKFSSKPEIGRVIVGVCSAIGAADGDFDEHEKAVVRNICSVLGLSPSEFSL
>NZ_CP009285|399667:406835|403449_404172_+|WP_042218807.1|DBSCAN-SWA
MISVKHLHKSFGAHKVLSDISVDIHSREVVVVIGPSGSGKSTFLRCLNLLEQPQEGDIIIEGTSLMAKSTRINDIRTEVGMVFQQFNLFPHKKVIENIMLAPMQVRKWPADKARQKALELLQKVGLSEKAEMYPSSLSGGQAQRVAIARALAMEPKIMLFDEPTSALDPEMVGEVLAVMKDLAREGMTMVVVTHEMGFAREVGDRVLFMEQGIIVEQGAPEQLFGNPSHERTQEFLSKVL
>NZ_CP009285|399667:406835|401860_402676_+|WP_081971875.1|DBSCAN-SWA
MGIRKKWAMSGMVALLVLAMVGCGSNNNAGSGDAAGESIKFASDASYAPMEYMDTDTIKGFDIDFIKAVMEEAGIDYTVTNTGWDTMLTSVQQGTEYQAGLSSVSITDERKETYDYSIPYFESTNMIMVKEGSDIKSALDLKDKKVAVQAATTADDLMSGIMGIDNGNLKRFDSNAVALMELNGGGADAVVADIAIVNEYIKNNPNEKLVGIIDKENFGSEYYGILYPKGSEWKAKLDPAIKTIIENGKYAEIYKEWFGEEPDTKTLLSAE
>NZ_CP009285|399667:406835|400724_401600_+|WP_042210159.1|DBSCAN-SWA
MRKVKVAATQMSCSGDIDENIRKAETLVREAAAQGAQIILLQELFETPYFCQKEKSDYYAYATELEHNKAVNHFKAIAKELEVVLPISFYEKKNYARYNSLAVIDADGTVMGKYRKSHIPDGPGYEEKFYFNPGDTGFKVWNTRYAKIGVGVCWDQWYPEAARVMSLMGAEILFYPTAIGSEPQDGSIDSKDHWQTCMLGHAAANLIPVVASNRIGEEIDEDSSINFYGSSFIAGPQGNKIAEAGRDEQTVLVSEFDLDALEVGRIEWGIFRDRRPELYRLIASYDGDLTF
>NZ_CP009285|399667:406835|399667_400702_+|WP_042210158.1|DBSCAN-SWA
MTYPKDLNYTMPAEWARHERTFISWPVQDSMVYPDNHAAVSAGYAEIIKAIAEFEPVTVVVNPGDMETVEQLGLGANVTLLPIKHNDAWLRDNGPTFVVNNEGKLAGVNWKFNAWGGKYSPWDLDDKVAPQILEQLEISSFDAPLVMEGGSIHTDGEGTLLTTEECLLNTNRNPELDREEIAGLVKRYTGTESIIWLKRGLSGDETDGHVDNIACFAAPGKVVIQVCGDPEDENYAISEENLRILEQAVDAKGRKLEIIRIQQPPRVDYEDSRLTLSYLNFYFVNGGIILPVFGGTAAETDKLAEETLAGLFQGRRIRTVNGMAVIGEGGNVHCTTQQMPAVKS
>NZ_CP009285|399667:406835|402786_403434_+|WP_042210160.1|DBSCAN-SWA
MDFRFDIIVHYLPVLLKGTLFTIGVSLVSILCGSILGLVIGFGKMAPKWYFRWPFHAYINIFRGTPLYVQILIVHFGLIPLFYGKTYALMSAFVALSLNSAAYSAEIFRAGIQSIDPGQREAALSLGMTKLQAMRFIILPQAIKRMVPAFGNEFIVLVKDSSLLALIAAPEIMYWSNTMKGQYLRIWEPYLTAALIYFILTYSLSKLLNYIERKV
>NZ_CP009285|399667:406835|406253_406835_+|WP_042210164.1|DBSCAN-SWA
MTISLSKGQRIDLTKTNPGLTKVVVGLGWDTNKYSGGKDFDLDASAFLLHEDGKAKGEDDFVFYNNPSGGTGSVTHTGDNRTGEGDGDDEQILVDFSLVPANIQRIGITVTIYDYETRVQNFGQVSNAFVRVVDASSDREILRFDLGEDFSTETAVVFCEFYRHGTDWKFQAVGSGFAGGLSALCKNYGLDAQ

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042210158.1|399667_400702_+	agmatine deiminase family protein	M1I5R4	Acanthocystis_turfacea_Chlorella_virus	1.8e-63	37.5
WP_042210159.1|400724_401600_+	N-carbamoylputrescine amidase	M1GUG4	Paramecium_bursaria_Chlorella_virus	2.5e-74	48.5
WP_081971875.1|401860_402676_+	transporter substrate-binding domain-containing protein	NA	NA	NA	NA
WP_042210160.1|402786_403434_+	amino acid ABC transporter permease	NA	NA	NA	NA
WP_042218807.1|403449_404172_+	amino acid ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	1.7e-23	31.3
WP_042210161.1|404426_404873_+	tellurite resistance TerB family protein	A0A1Y0T181	Sinorhizobium_phage	4.0e-07	29.3
WP_042210162.1|404999_405596_+	TerD family protein	K4JRX3	Caulobacter_phage	5.8e-22	33.2
WP_042210163.1|405625_406201_+	TerD family protein	NA	NA	NA	NA
WP_042210164.1|406253_406835_+	TerD family protein	K4JRX3	Caulobacter_phage	1.5e-27	37.0

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP009285|761813:773776|DBSCAN-SWA
TATGATCGAACGTTACAGCAGACCTGAGATGCGGGCCATTTGGACCGAAGAAAATAAATTCAACGCGTGGCTGGAAGTTGAAATTTGCGCCTGCGAGGCTTGGGCCGAGCTGGGAGTCATCCCGCATGAGGATGCCGCGAAGCTGCGCAAGGATGCCAAATTCGACATCGCGCGGATTGATGAAATCGAGCAGGAAACACGTCATGATGTTATTGCTTTTACCCGTGCAGTATCGGAGAGCCTGGGCGCAGAACGCAAATGGGTGCATTACGGACTGACCTCCACAGACGTTGTCGACACGGCGCTCGGCTATCTGCTGCGTCAGGCCAACGAAATTCTGGAGCAAGACATTATCCGGTTCATTGAGATTCTAAAAGATAAAGCAGTAGCCTACAAAGATACTCCGATGATGGGGCGCACCCATGGCGTACACGCCGAGCCGACGACTTTCGGCCTCAAGATGGCGCTGTGGTATGAGGAAATGAAGCGCAATCTGGAGCGTTTCCGTCATGCCGCTAACGGCGTACAATTCGGCAAAATCTCCGGGGCAGTCGGCACCTATGCCAACATCGACCCGTTCGTCGAAGAATTTGTCTGCCGCAAGCTGGGCACCAGCCCGGCACCGATCTCCACGCAGACACTGCAGCGTGACCGTCACGCTGAATACATGGCGGCGCTGGCACTGGTTGCCACTTCGCTGGACAAGTTCGCTACCGAGATCCGCGCGTTGCAGAAGAGTGAGATCCGCGAGGTGGAAGAAGCTTTTGCCAAAGGTCAAAAAGGTTCGTCCGCGATGCCGCATAAGCGCAACCCGATTGGCTGCGAGAACATCTCCGGCCTGTCCCGCGTGATCCGCGGGCATATGGTTACAGCTTACGAGAACGTGCCGCTGTGGCATGAACGTGATATCTCGCATTCCTCGGTAGAACGGATCATCCTGCCGGACGCGACTATGCTGCTGAACTATATGCTGAACCGCTTCGGCAACATCGTGAAGAACCTGACTGTGTTCCCGGACAATATGAAGCGCAACATGAACCGCACCTTCGGCGTACCGTTCTCCGGCCGCATCCTGACGAAGCTGATCGACAAAGGCTTCAGCCGCGAGCAGGCTTACGACACCGTGCAGCCGCGGGCGATGCAGGCCTGGGAGGAACAAACCCAGTTCCGTGACATCGTTGAAGCTACACCGGAAATCACAGCCGTGCTAAGTCCGGAAGAGATCGAGGATGCGTTCAATCCTTCCTGGCACCTCAAGCATGTGGACACCATCTTCCGCAAACTTGAGCTTATCTAATTAAAAAAGGTGAGTCAGTGGTGAACTGATGAGCTGGAGAAGAGATGGGCGGAGCGATGGGGAGTTTTGTTCCCGGGAAGCGTAGCAACAGGGGAATAAGATTAGGTATTAGGGTTAAAGGAGGAACGGAGAGGAATTTTGGAACTGTAGAAGCTTTAGCGTTCGCCTTTATGTTTGGATTTCTACCGCAGCCGGCGGTTCAAATCAGGAAATTCAAACATAACAGCGATCGGAAGTCCAAAATTCCCCGCAGTGACACTATTAACCCGAAGGAGCTTTCAATTCCTTTGGTGCGAAGCGAAGGAAACAAAGCGTCCCTGCGCTTTTAGCCCAAATATAAGCAAGATCATTTGTTCAAGGGAGGAAAGGTCATGACATCAACGGCCGTATCCACTGCCGTGGAACTCGTAAATGCACCGCTGCTCTACAAAGGTAAGGTTCGTGAGCTGTACGATTTGGGGGATGAGGTACTGATTGTCGTTACGGACCGCATTTCCGCATTTGATTATGTGCTGGACCCGGCGGTGCCGGACAAAGGCAATGTGCTGAACCGGCTCAGCGCCTTCTGGTTTGGCCAGACCAAGGAGCTCATTGAGAACCATGTAGTTCACATCGATGTGGACCGGCTCGGAGATATTGTACGGGACCGCGAAGCGCTGAAGAACCGCATCATGGTGGTCCGCAAAGCACAGCGGATTGATATCGAATGTGTCGTGCGCGGCTGCATTACCGGCGGCGGCTGGCGGCAGTATCAGGAGACCGGCAAAGTGAACGGCATCGAGCTTCCCAAAGGGCTGCGCAAGAATGCGGTGCTGACCGAGCCGATCTTTACGCCGGCGGCCAAGAATGATGTCGGCCATGATGAGGATATCCCTTTTGAGCAGATGCAGGAGTTAATTGGCGCAGAGCTTGCGCTGGAGCTGAAGGAGAAGAGCCTGAAGCTGTTCGCTTTTGCCAGAGAATATTGTAAAGACCGCGGCATCATCCTCGCCGATTGCAAATTCGAGTTCGGGCTGCTGGACGGTAAGGTCATTCTGATCGACGAGATTTTCACACCGGATGCTTCCCGTTTCTGGGCTAAGGACAAATACGCGCTGGATATCGAGATCGATAGCATGGATAAGGAGCCTGTACGGACTTACCTTTCGGCATCCTCGTGGGACAAGAACAGTACACCGGACCCGCTGCCGGTTGAAGTGGTGGAAGAGACCTCACGCCGGTACCTGGATATTTATCACCGCCTTACCGGAAAGTCCTTATAGATTATCTGATGCTCCTGTTCCGACCAGCTGCAGCTAACTTTTAATTGTATTCTCTGCAGTTATTTTGCCCGAAAAAGATGCCATTTGCTCTTTAACTGTATCTGGTACAACTAAAAATAAGCGAGACGGCCTGAAACGCAGATTTCCTTAGAAATAGCTGTATGAAATGCAACTAAAGCTGATTTTGCAGGAGTCATTGAGAGAATAGCTGTACATTATGCAGTTAAGTTAGCTGTCAGCAGTGAAGTGAGTTGTTGCAGCTCACCGTTAGAGGTTAGCACATTGTTGTAATGTTGAATTACGGTAAGTTTTCATTCCAGGTACCCAGTCCAGCTCATTAAATTTTAGGAGGAACTACAAGCGTATGTTAAAAGCGACAGTCTACGTCACCATCAAGAAAAGCGTGCTCGATCCCCAAGGTGTAGCCGTGCAAGGGGCGCTGCATTCCGTAGGTTTTCAGGAAGTTGAAAGTCTGCGTATCGGCAAATATATGGAGCTGACCCTCGATACCGATAACCGCGCTGAAGCGGAAGGACGCCTCAAGGATATGTGCGAGAAGCTGCTGGCCAACACGGTGATCGAGGATTACCGCTACGAATTGGAGGACTAAAAGTCATGAAATTTGCGGTACTTGTCTTTCCAGGCTCCAATTGTGACATTGACTGCTACAAGGCAGTAGAAGACAGCCTCGGTGAACCAGTGGATTATGTGTGGCATACGGCGACGGATCTGTCGGCTTATGACTGCATTCTCGTGCCGGGCGGCTTCTCTTATGGTGACTATCTGCGCTGTGGCGCGATTTCCCGGTTTGCTCCGGTTATGGCGGAAGTAGCCAAAGCTGCGGAGCAGGGCAAATTCGTGCTCGGCATCTGCAACGGGTTCCAAATCCTGACCGAAGCGGGCCTCTTGCCGGGCGCGCTGCGCCGCAACATGTCGATGAAGTTCCGCTGTCATGACACGGTGCTTAAGGTCGTGAATAACACAACCCCGTTTACTATTGACTATGCGAAGGATGAAGAGATCGTCATTCCAATCGCGCATGGGGAAGGCAATTACTACTGTGATGAAGAGACTTTAGCTGAATTAAAAGCAAATAATCAGATCGTATTCACATACAGCGACAACCCGAACGGTTCAGTCGCCGATATCGCCGGAGTCAGCAATGTAGCAGGCAATGTGGTTGGTATGATGCCTCACCCGGAACGTGCAGCGAACAGCCTGCTTGGTTCGGAAGACGGCAAACGGATGTTCACATCCATTCTTACATCGTGGAGGGATCGTTATGACGCAGCAAGTATCCGCTAAGGAGCCGACCGCAGAGCAGATCGCGGAGCAGAAAATCTACAGTCAGTTCGGTGTATCGGACAGCGAATATGAGCTCATTACTTCCTTCATGGGACGTAAGCCTAACTATACAGAAATCGGTGTGTTCAGCGTAATGTGGTCCGAGCACTGTGCCTATAAGAACTCGAAGCCGCTGCTCAGCCGTTTCCCGACTAGCGGGCCGAAGGTGCTGATGGGACCGGGCGAAGGCGCAGGTATCGTTGATATCGGAGACAACCAGGCGGTAGTCTTCAAGATCGAGAGCCACAACCACCCGTCGGCAGTTGAGCCTTATCAGGGCGCGGCGACCGGGGTGGGCGGGATTATCCGCGATATTTTCTCCATGGGGGCAAGACCGGTGGCGCTGCTGAACTCCCTGCGTTTCGGGAAGCTGGAGAGCGACCGGGTAAAATATTTGTTCGAGCATGTTGTGTCCGGTATCGCAGGCTACGGCAACTGTATCGGCATCCCTACCGTCGGCGGGGAAATTATGTTCGACGACAGCTATGACGGCAATCCGCTTGTTAATGCAATGTGTGTGGGGCTGATTGATCATGATAAAATCCAGCGCGGTGTCGCCAAAGGGGTTGGCAATCCCGTGTTCTACGTGGGTCCTCCTACAGGCCGTGACGGCATTCATGGTGCGACGTTCGCCTCGGTTGAGCTTAGCGAAGAGTCTGAAGCGAAGCGGACGGCAGTCCAGGTTGGCGATCCATTCATGGAGAAGCTGGTTATGGAATCTTGTCTGGAGCTGATCGACAGCGGCATCGTCCTCGGTATTCAGGATATGGGCGCAGCCGGACTTACCTGCTCCAGTGCTGAAATGGCGAGCAAAGCGGGCAACGGTCTGGAGCTGTATCTGGATCAGGTGCCGCAGCGCGAAGACGGCATGACTCCATATGAAATGATGCTCTCGGAATCCCAGGAGCGGATGTTGTTCGTAGTTGAGCCTAAGGATGAAGCGCAGGCACAGGAAATCTTCGACCGCTGGGGCGTCATCTGCCGCAAAGTGGGTAAGGTAACGGATGACGGCCGGCTGAAGCTGTTCCATCACGGTGTAGTTGTCGGCGACATGCCGGTAACGGCTCTGGTTGATGAATGTCCGATCTACAACAAACCATCAGCAGTTCCTGCGTACTATGAAGAAAATGCATCGGTTGATACGCTCCGCTATGAAGAAGTAACCGATCTGGGCGGCGCTCTGCGCACCGTACTAGGATCACCTACAGTAGCCAGCAAAGCATGGGTATACAACCAATATGATTATATGGTTCGGACCAGCACGGCCGTTCGTCCGGGTTCCGATGCGGCAGTGGTAACCATCCACGGTACTCGCAAAGGTCTAGCTATGACTACGGACTGTAACGGACGTTATGTGTATCTCGATCCTGAAGTGGGCGGACGGATTGCCGTCAGCGAAGCCGCACGTAACATTGTCTGTTCCGGTGCTCTGCCGCTGGCAATTACGGACAACCTGAATTTCGGCAGTCCGGAGAAGCCGGAAATCTTCTGGCAGATGGAACGTGCGGTAGACGGCATGGCTGAAGCCTGCCGTGTGCTTGATACCCCTGTAATTGGCGGTAACGTCAGCCTATACAATGAAAATGCTTCAGGAGCCATCTACCCGACACCGGTTGTCGGCATGGTAGGTCTCGTGGAGGATACCGATCATATTACAACTCAGGCCTTCAAGCAGGAAGGCGATGCGATTCTGCTGCTCGGTGTTACGAAAGCAGAGCTGGGCGGCAGCGAATTCCAGTATGCTGTTCACGGTGTGACCGAAGGACGTCCGCCGGAACTCGATCTGGCCACTGAACGCAAGCTGCTGGATTCCGTACTTGCTGCGATCCGCAGCGGGCTGGTCCGCTCGGCGCATGACCTGTCCGAAGGCGGCCTGGCCGGAGCACTGGCAGAAAGCTGCATCAGCGGCAAAACCGGAGCCAATATTGAGCTGTCTGCTGGCGGATTGCGCCCTGATGTGGCGCTGTTCAGCGAGAGCCAATCCCGGATTATCCTGACTTCGGCACCTGACCGTGCGGAAGAACTGAAAGCAGCGGTTGCCGCATATGGCGTGCCTGTAGAGATTATTGGAACCGTCGGCGGAGACCGCCTGCGTGTTGCATTGGACGGCGCGTCTGCACTTGATGAAGCAGTTACTGAACTCAAGACCATTTGGGAGGATGCTATTCCATGTCTTATGAAATAAAGACCGGGAAAGAGCAGGAAGCCCCTATCCTGTGGACCGGCGACTTTTACAACGAAGGAACGGGCTCGGGAGATATTTTTGACACATTAAAAGAAGAATGCGGCGTCTTCGGGGTCTTCGGACACCCGGAAGCCGCTTCCATGTCCTATTACGGCCTGCATGCCCTGCAGCACCGCGGGGAAGAGAGCGCGGGCATCTGCGTAGCGGATGGACGCGACTTCAACTATCACCGCGGCATGGGCCTGGTGAAGGAAGTCTTCGACAAAGACAAGATTGCTTCGCTGATCGGGGACATGTCCATTGGACATGTGCGCTATTCGACCAGCGGAGACAGCCGGCTGACCAATGCGCAGCCGCTGGTCTTCAAATACCGCGACGGTGATCTTGCGATTGCCACGAACGGCAACATTGTCAACGAACCGCTCATCCGCAAGCAGCTTGAGCAGGGCGGTTCAATCTTCCAGACCACCAGTGATACCGAAGTGCTGGCGCATTTGATCGCGCGTTCGCAGAAGGATTTTGTTGAAGCGACCAAGGATGCCCTGGCGCAGCTGGTTGGCGGGTTCGCCTTCCTGCTGATGACCAATGACAAGCTGATTGTTGCTTCTGATCCGCACGGACTCCGTCCGCTCGTAATGGGCCGGCTGGGTACGGCGTACGTCTTCGCTTCCGAGTCCTGTGCGCTCGAAGTCATTGGCGCTCAGCTTGTGCGCGATATTGAGCCTGGCGAGCTGCTGGTGCTGGATAAAGACGGCTTCCGGGAAGACCGCTTCGCAGAACCTAAACGCAAAGCGCTGTGCGCGATGGAATACATCTACTTCGCACGGCCGGACAGCGATCTGAACGGCTCCAACCTGCACTCCGCACGCAAGCGGATGGGCAGCCGGATGGCGCTCGAAGCCTTCGTGGATGCCGATATCGTAACCGGCGTGCCGGATTCCAGTATCTCCGCTGCTATCGGCTATGCCGAGCAGACAGGCATCCCGTATGAGCTTGGTCTGATCAAGAACAAGTACACCGGCCGGACCTTTATCCAGCCGAGCCAGGAGCTGCGCGAGCAAGGCGTGAAGATGAAACTCAGCGCCGTGCGCCGCGTTGTGGAAGGCCAGCGCGTAGTCATGATCGACGATTCCATCGTGCGCGGCACGACCTCACGCCGGATCGTCAACCTGCTGCGCGAGGCCGGAGCGGCCGAGGTTCATGTGCGGATTACTTCGCCGCCGTTCAAGAATCCGTGCTTCTATGGCATCGATACCCCTGACCGCCGCGAGCTGATCGCCTCTTATAAGACGATTGCCGAGATGTGTGAGGAGATCAATGCTGACTCGCTTGCGTTCCTCTCGCCGGAGGGACTCATCCAGTCCATCGGCGGCTATAATAGTGACAATTACAAAGGCGGGCTATGCCTGTCCTGCTTCGATAATGATTACCCGACGCAGGTTGATTTCGGCGGGGAAGAGAAGGACGGATGCTCGTGCTAGGTGGGACATCCCTGTCGGAATACGCCATTCTTTACACTAGATTCGTATTAGAAGTATGAAGACATTTTAATAAGCGCTGTAGAAATAAATGTTGTATGTTTTGCAACTTGAGTCCTTGGATAGGCGGGTGTTTGGGAGGATTGTTGTATCAAATACAACATTTAATCAGGAAAAGCGACTTAAAAAGGGTGAAATCCTGCATTTTGTACAACAATTTCGGATTTGGGCCGATCTAATGAGCGAAATGTTGTATTCTGTGCAGGATTTTATGAAAAGATAACCGATCAATGCCCTGCAAAGCGGAGGAATCGACGACTTCCTGTGACAAACAGCCGCCGCCGGGCTTAAAGCTCCGCTTCCGTCCTGTTTGCTGTCGCAAACTAAGGATGCGGGACGACTATCTTCGTACGCTTAGGAGGCGCTGTGCGAAGCCCAGCGCCGACCAATTGCTGCTGTGCAAGGCGCGAAATTTCGGCTTGCGGCACGGGTTTGACCTGGTGGTTTGGAAGTTATGGAGAGGGATTTTGGAACTGTAGGAGCGTCAGCGTTCGCCTTTATATTTGGATTTCTACCGCGGACAGCAGTTCAAATCAAGGAAATCCAAATATAACAGCGACCGGAAGTCCAAACATCCATCGCAATAACATCCACAAACCACACTCAATGCCCTGCCGCCCCGAACCCGCGCTCTAAACTAATTTAAATGAGGTGTCCAAAAGTGTCGGAAGCTTATAAAAACGCCGGAGTGGATATTGCGGCTGGCAATGAAGCGGTAGAACGCATGAAGAAGCATGTGAAGCGCACATACCGTCCTGAAGTGATGACGGAGCTGGGCGGATTCGGTGCACTGTTCGGCCTGAATAAGGACAAGTACGAAGAGCCGGTCCTCGTATCGGGAACGGACGGCGTAGGCACGAAGCTCAAAATCGCGTTCGCCGCGGACCGCCACGACACGATTGGCATCGATGCGGTAGCCATGTGTGTGAATGACATCGTAGTGCAGGGCGCAGAGCCGCTGTTCTTCCTCGACTATCTGGCCTGCGACAAGGTAGTGCCGGAGAAGATTGAGGCGATCGTTGCCGGTATCGCCGAAGGCTGCCACCAGGCAGGCTGCGCCTTGATTGGCGGCGAAACGGCCGAGATGCCGGGTATGTATTCGGCCGGTGAGTACGATATCGCCGGATTTACCGTAGGCGTTGCCGACAAAGCGAAGCTGGTAACGGGAGCGGACATTGCTCCGGGAGACACGGTAATTGGCCTGGCTTCCAGCGGTATCCACAGCAACGGATTCTCGCTCGTGCGCAAGCTTCTGCTGGAGGAAGACGGCTATGGCTTGAACGATGTAGTGCCTGAGCTGGGCGCTCCGCTCGTGGATGTACTGCTGGCTCCAACCAAAATCTATGTGAAGCCGCTGCTGTCCCTGCTGGAACAGCTTCCGGTTAAGGGCATGGCTCATATTACCGGAGGCGGGTTCATCGAGAACATCCCGCGCGTCCTGCCGGAGAATGTGAATGTAGAGATTAACTACGGCTCCTGGCCGATTCAGCCGGTCTTCGGCTTGATGCAGAGCAAAGGCAATGTAAGCAACCGCGATATGTTCACCACTTTTAACATGGGTGTTGGCCTGGTACTGGTAGTGGCTGAAGCGGACGGAGAACGTGCGCTGGAGCTGCTGAAAGCGAGCGGAGAAGAAGCTTACCTTATCGGTACTGTAACAGAGGGTGAGCGTAAGGTTACCTTTACGGGAGCTGAAGTCTGATGGAGTGGAGCCGGATCGCTGTATTTGCTTCGGGACAGGGCAGCAATTTCACCGCACTGGTCCAGGCGCAGCAGGAGGGGAAGCTTGGCGGGGGCAGCATTGAGCTGCTCGTCTCGGACAAGCCGGAAGCGCCTGTGGCACAGCGGGCGGAGGCAGCGGGAATTCCCGCCCTCCTGCTGCGGCCGAAGGACTTCGCGGGCCGTGAGCTGTATGAGGCGGCAATTGTTGCCGAGCTGCAGCGCCGGAACATCGGGCTGATAGTGTTGGCCGGATACATGCGGCTGATCTCATCTGTGCTGCTTGAGCCTTACGCCAGACGGATCATCAACATCCATCCGTCGCTTTTGCCGGCCTTCGCCGGTAAAGATGCGATCGGTCAGGCCCTTGAGTACGGGGTGAAGCTGACGGGAGTTACGGTGCATTTTGTCGATGGAGGCATGGATACCGGACCGGTTATTGCCCAGCGCAGCGTTGAGGTGAAACCGGGAGATACCGCCGAATCCCTGGCGGAACGGATCCACCAGGTTGAATATGGGCTGTATCCCGAAGTGGTGGCTGCTTTGGCAGCAGGCAGAGTGGAACTGAATGGAAGAATAACAACAATCGGCGAATAATAGGATGCGATACGAGCCGGATCTGACACAAATAGATATATTACAGGCAGGTGCGGCTGCTTCTGATATTTCTCGGGAAATATTGCACAAAGTCTGCAAGATGTCGGATTGGCAGGCTGAGCAGTTTGAAATTGCCGAAATTGCGGATTTGCTGACATGCTGGCTAATGTCGATATAGCAGTTGGATTCACTCCACTTAATTTGTCTGAATACCAGCGGTCGCGAAACGTAAGTGGATAAAGTACAACTAAATTTGGCGTTGTAGGCTCTAAGGCGCATATGGCATCATTTAGATGGACAATTTCCAACTAATTTCTATCCGGCGGATAACAAGCCGAAATTAAATGACGTAAATCCACTTATTTTATAAACACTATAGACTCAAGTTATAAGCACGGGCTAATCGGCGACACAGATCCTGCGATCATAAGCCACAACCTATTCTAGCGTGAATCCAGAGGAGGACTATTCAAAGTGAGTATCAAAAGAGCACTGGTCAGCGTATCGGACAAACAGGGCATCGTGGATTTTTGCCGCGAGTTGTCTGCACTAGGCGTAGAAATTATCTCCACAGGCGGCACCAGCACACTTCTGGCTAAAGAAGGCGTTCCGGTCATCGGTATATCCGATGTGACGGGCTTCCCCGAAATTATGGACGGACGCGTCAAAACACTGCATCCCGCTGTACACAGCGGCCTCCTTGCGGTTCGTGATAACGAAGAGCACACACGGCAGATGACCGAGCTTGGACTTGACTACATCGACCTCGTAGTGGTGAATCTGTATCCCTTCGCGGAAACCATTGCCAAGCCGGATGTATCGTATGAAGAAGCTATCGAGAACATCGATATCGGCGGACCTACGATGCTGCGTTCGGCGTCGAAGAACCATGCTTTTGTCAGTGTGGTTGTGGATGCGGCGGATTATGCTACAGTGCTTGAGGAAGTTCGTGCGGGTGGAGATACCACCCTTGCAACCCGCAAACGTCTTGCGGCCAAAGTCTTCCGCCATACGGCGGCTTACGATGCCCTGATTGCTGATTATCTGGCGAATGTAACCGGTGAACCGCTGCCGGAACGCTATACGGTCACTTACGAGAAAATCCAGGATCTGCGTTACGGGGAGAACCCGCACCAGAAGGCTGCGTTCTACCGCAAGCCGCTGGCTGCGCAGGATACACTCACCGCTGCTGAGCAATTGCACGGCAAGGAGCTGTCCTACAACAACATCAACGATGCCAATGCAGCACTTCAAATTGTAAAAGAGTTCGAAGAACCGGCTGTTGTAGCTGTTAAGCATATGAATCCTTGCGGCGTAGGCGTGGGTGCGAGTGTATATGAGGCTTATCAAAAAGCATACAATGCCGATCCAACCTCCATCTTCGGCGGAATTGTAGCGGCGAACCGGATCATTGATGAAGATACGGCTAATATGCTGAAGGATATTTTCCTTGAGATCGTTCTGGCTCCGGGCTTCACGGAAGAAGCACTGGAAATCCTGATGAAGAAAAAGAATATCCGCCTGCTCAAGCTGGGCAACCTCAGCACGGCGGCTTCCCGTAAAACCAGCTTTGTCGTAACCTCCATTGAAGGCGGAATGGTCGTGCAGGAAAGTGACGTGCATTCCGTGAATCCGGAAGAGCTGCAGGTCGTAACCGACCGCAAGCCGACGGAAGAAGAGCTTAAGCAGCTGCTCTTCAGCTGGAAGGTGGTTAAGCATGTGAAGTCGAACGCGATTGTGCTGGCGGCTGATAATATGACCGTAGGCGTAGGGGCAGGACAGATGAACCGTGTCGGCGCGGCTAAGATTGCGATTGAACAGGCCGGAGAGAAATCCAAAGGCTCCGTGCTGGCTTCCGATGCCTTCTTCCCGATGGGCGATACACTGGAGATGGCTGCCAAGGCTGGTATTACGGCAGTTATTCAGCCGGGCGGGTCGATTAAGGACGAGGAATCCATTAAGGTTGCTAATGAATACGGCATTGCCATGGTCTTCACCGGCGTTCGCCATTTCAAACACTAG

Protein sequences of DBSCAN-SWA_2

>NZ_CP009285|761813:773776|764735_764981_+|WP_039298247.1|DBSCAN-SWA
MLKATVYVTIKKSVLDPQGVAVQGALHSVGFQEVESLRIGKYMELTLDTDNRAEAEGRLKDMCEKLLANTVIEDYRYELED
>NZ_CP009285|761813:773776|765653_767900_+|WP_042210459.1|DBSCAN-SWA
MTQQVSAKEPTAEQIAEQKIYSQFGVSDSEYELITSFMGRKPNYTEIGVFSVMWSEHCAYKNSKPLLSRFPTSGPKVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPYQGAATGVGGIIRDIFSMGARPVALLNSLRFGKLESDRVKYLFEHVVSGIAGYGNCIGIPTVGGEIMFDDSYDGNPLVNAMCVGLIDHDKIQRGVAKGVGNPVFYVGPPTGRDGIHGATFASVELSEESEAKRTAVQVGDPFMEKLVMESCLELIDSGIVLGIQDMGAAGLTCSSAEMASKAGNGLELYLDQVPQREDGMTPYEMMLSESQERMLFVVEPKDEAQAQEIFDRWGVICRKVGKVTDDGRLKLFHHGVVVGDMPVTALVDECPIYNKPSAVPAYYEENASVDTLRYEEVTDLGGALRTVLGSPTVASKAWVYNQYDYMVRTSTAVRPGSDAAVVTIHGTRKGLAMTTDCNGRYVYLDPEVGGRIAVSEAARNIVCSGALPLAITDNLNFGSPEKPEIFWQMERAVDGMAEACRVLDTPVIGGNVSLYNENASGAIYPTPVVGMVGLVEDTDHITTQAFKQEGDAILLLGVTKAELGGSEFQYAVHGVTEGRPPELDLATERKLLDSVLAAIRSGLVRSAHDLSEGGLAGALAESCISGKTGANIELSAGGLRPDVALFSESQSRIILTSAPDRAEELKAAVAAYGVPVEIIGTVGGDRLRVALDGASALDEAVTELKTIWEDAIPCLMK
>NZ_CP009285|761813:773776|761813_763109_+|WP_042210452.1|DBSCAN-SWA
MIERYSRPEMRAIWTEENKFNAWLEVEICACEAWAELGVIPHEDAAKLRKDAKFDIARIDEIEQETRHDVIAFTRAVSESLGAERKWVHYGLTSTDVVDTALGYLLRQANEILEQDIIRFIEILKDKAVAYKDTPMMGRTHGVHAEPTTFGLKMALWYEEMKRNLERFRHAANGVQFGKISGAVGTYANIDPFVEEFVCRKLGTSPAPISTQTLQRDRHAEYMAALALVATSLDKFATEIRALQKSEIREVEEAFAKGQKGSSAMPHKRNPIGCENISGLSRVIRGHMVTAYENVPLWHERDISHSSVERIILPDATMLLNYMLNRFGNIVKNLTVFPDNMKRNMNRTFGVPFSGRILTKLIDKGFSREQAYDTVQPRAMQAWEEQTQFRDIVEATPEITAVLSPEEIEDAFNPSWHLKHVDTIFRKLELI
>NZ_CP009285|761813:773776|764986_765676_+|WP_042210457.1|DBSCAN-SWA
MKFAVLVFPGSNCDIDCYKAVEDSLGEPVDYVWHTATDLSAYDCILVPGGFSYGDYLRCGAISRFAPVMAEVAKAAEQGKFVLGICNGFQILTEAGLLPGALRRNMSMKFRCHDTVLKVVNNTTPFTIDYAKDEEIVIPIAHGEGNYYCDEETLAELKANNQIVFTYSDNPNGSVADIAGVSNVAGNVVGMMPHPERAANSLLGSEDGKRMFTSILTSWRDRYDAASIR
>NZ_CP009285|761813:773776|770099_771140_+|WP_042210462.1|DBSCAN-SWA
MSEAYKNAGVDIAAGNEAVERMKKHVKRTYRPEVMTELGGFGALFGLNKDKYEEPVLVSGTDGVGTKLKIAFAADRHDTIGIDAVAMCVNDIVVQGAEPLFFLDYLACDKVVPEKIEAIVAGIAEGCHQAGCALIGGETAEMPGMYSAGEYDIAGFTVGVADKAKLVTGADIAPGDTVIGLASSGIHSNGFSLVRKLLLEEDGYGLNDVVPELGAPLVDVLLAPTKIYVKPLLSLLEQLPVKGMAHITGGGFIENIPRVLPENVNVEINYGSWPIQPVFGLMQSKGNVSNRDMFTTFNMGVGLVLVVAEADGERALELLKASGEEAYLIGTVTEGERKVTFTGAEV
>NZ_CP009285|761813:773776|763480_764371_+|WP_042210455.1|DBSCAN-SWA
MTSTAVSTAVELVNAPLLYKGKVRELYDLGDEVLIVVTDRISAFDYVLDPAVPDKGNVLNRLSAFWFGQTKELIENHVVHIDVDRLGDIVRDREALKNRIMVVRKAQRIDIECVVRGCITGGGWRQYQETGKVNGIELPKGLRKNAVLTEPIFTPAAKNDVGHDEDIPFEQMQELIGAELALELKEKSLKLFAFAREYCKDRGIILADCKFEFGLLDGKVILIDEIFTPDASRFWAKDKYALDIEIDSMDKEPVRTYLSASSWDKNSTPDPLPVEVVEETSRRYLDIYHRLTGKSL
>NZ_CP009285|761813:773776|772228_773776_+|WP_042210465.1|DBSCAN-SWA
MSIKRALVSVSDKQGIVDFCRELSALGVEIISTGGTSTLLAKEGVPVIGISDVTGFPEIMDGRVKTLHPAVHSGLLAVRDNEEHTRQMTELGLDYIDLVVVNLYPFAETIAKPDVSYEEAIENIDIGGPTMLRSASKNHAFVSVVVDAADYATVLEEVRAGGDTTLATRKRLAAKVFRHTAAYDALIADYLANVTGEPLPERYTVTYEKIQDLRYGENPHQKAAFYRKPLAAQDTLTAAEQLHGKELSYNNINDANAALQIVKEFEEPAVVAVKHMNPCGVGVGASVYEAYQKAYNADPTSIFGGIVAANRIIDEDTANMLKDIFLEIVLAPGFTEEALEILMKKKNIRLLKLGNLSTAASRKTSFVVTSIEGGMVVQESDVHSVNPEELQVVTDRKPTEEELKQLLFSWKVVKHVKSNAIVLAADNMTVGVGAGQMNRVGAAKIAIEQAGEKSKGSVLASDAFFPMGDTLEMAAKAGITAVIQPGGSIKDEESIKVANEYGIAMVFTGVRHFKH
>NZ_CP009285|761813:773776|771139_771754_+|WP_042210463.1|DBSCAN-SWA
MEWSRIAVFASGQGSNFTALVQAQQEGKLGGGSIELLVSDKPEAPVAQRAEAAGIPALLLRPKDFAGRELYEAAIVAELQRRNIGLIVLAGYMRLISSVLLEPYARRIINIHPSLLPAFAGKDAIGQALEYGVKLTGVTVHFVDGGMDTGPVIAQRSVEVKPGDTAESLAERIHQVEYGLYPEVVAALAAGRVELNGRITTIGE
>NZ_CP009285|761813:773776|767884_769381_+|WP_042218864.1|DBSCAN-SWA
MSYEIKTGKEQEAPILWTGDFYNEGTGSGDIFDTLKEECGVFGVFGHPEAASMSYYGLHALQHRGEESAGICVADGRDFNYHRGMGLVKEVFDKDKIASLIGDMSIGHVRYSTSGDSRLTNAQPLVFKYRDGDLAIATNGNIVNEPLIRKQLEQGGSIFQTTSDTEVLAHLIARSQKDFVEATKDALAQLVGGFAFLLMTNDKLIVASDPHGLRPLVMGRLGTAYVFASESCALEVIGAQLVRDIEPGELLVLDKDGFREDRFAEPKRKALCAMEYIYFARPDSDLNGSNLHSARKRMGSRMALEAFVDADIVTGVPDSSISAAIGYAEQTGIPYELGLIKNKYTGRTFIQPSQELREQGVKMKLSAVRRVVEGQRVVMIDDSIVRGTTSRRIVNLLREAGAAEVHVRITSPPFKNPCFYGIDTPDRRELIASYKTIAEMCEEINADSLAFLSPEGLIQSIGGYNSDNYKGGLCLSCFDNDYPTQVDFGGEEKDGCSC

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042210452.1|761813_763109_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	2.0e-22	27.8
WP_042210455.1|763480_764371_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	5.4e-40	33.1
WP_039298247.1|764735_764981_+	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	2.2e-07	36.7
WP_042210457.1|764986_765676_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_042210459.1|765653_767900_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	2.3e-164	41.8
WP_042218864.1|767884_769381_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	1.8e-51	32.3
WP_042210462.1|770099_771140_+	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	1.4e-66	43.8
WP_042210463.1|771139_771754_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	6.4e-24	36.5
WP_042210465.1|772228_773776_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	5.9e-74	50.7

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP009285|2716326:2726578|DBSCAN-SWA
GATGAAACCGTTCCGCGTTCGGCTTACATTCATACTCATGGCCCTGATCGGGATATCCATGACCGGGGCTGGCATTACAATGGCCCAGCTGTTTAAGGATTCACATATTTCCGTGCTGGAAGAAAACATGTCCCGGGAAATAAATCTGCTCTCCGGCACGTTTACGTTCAAGGATATCCGCAGTCCGGATGCCATGGATTACTATACAGACCAGGCCCGGAAGATATCCACACTGACAGGTTCGCGGATCACCTTTATTACGAAGGAAGGCCGGGTTATCGGCGATTCGGAACGCAATCCGCTGGAAATGGACAATCACTCCACCCGTGAAGAAGAGCTGATCGCTGCAAAAGAAGGGATTGGCCGGGCGATCCGGTACAGTGATACGCTGGACCGCGAAATGCTGTATGTCGCTGGTGCGGTAGTCTCGGACCAGGGCTTCGACGGATATATCCGGCTGTCGATGGGACTGGATGCAGTCACGGAGGGGCTGAACCGGGCGTGGATGATCATGGCCGGCGGACTCGTGCTGCTCTTTATTGCGGCAACTTTTGTGAGCTATAAGGTGGCGTCCAGCATGACTTCACCGCTTGAGCAGATTACGAGAGTCGCGCGGCGTATCACTGATCTGGATTACGATGCCCGTGTGCCGATGAAGCGTAAGGATGAGATCGGCCAGCTGGCGACGGCGATCAATGCGATGGCGGACAGTCTGCAGGCCCAGCTGAAGACCATCCGCGACAACGAGGATCTGCTGCAAAGCGTGCTCGATAACATGACCGGCGGAATCGTGATGATTAACGCCGAAGGGGAGATTGCCCTGCTTAACCGGGCGGCGGAGCGGCTGCTTGATGTGAAGAACAGCGAGATGACCGGGCATTCCTACAAAGAGATCAAGCATCATTATGAGCTGACCCGTCTGATTGAAGAGGGCGTATCCGCAGGCGAGCCAGTCCATGAGGAGCGTATTATCTATAATCCGGTGGAGCGGATCGTACGTCTGGATGGGGTTCCGATGATTCAGGACGGCTCCACCCGGGGGATGCTGTTCCTGCTGCAGGAGGTTACGGAAATCCGCCGTCTGGAGAAAATGCGCAGCGAATTCGTCGCGAATGTCTCCCATGAGCTGAAGACCCCTGTAGCTGCGGTAAAAGGCTTCGCCGAAACCCTGCTAGGCGGAGGTGTTACGGATGAGAAGACAGCACGTTCATTCCTGCAGATTATTTATGATGAGAATGAACGGCTTAACCGCCTGATCGGAGACATTCTGGAATTGTCCAAAATCGAATCCAAACGCGTCCAGCTGGACTGCTCGCCGGTCCATCTAATCGAGTTCTTCGATTCTGTGCTGGAAACGCTCAGCAAGGTGGCAGAGAAGAAGAAGATTACACTCAGCTCAGATGTGCCGCCGGAGCTGTTCATTGAGGGGGATGAAGACAAGCTGCGGCAGATCTTCATGAATCTGCTCTCGAATGCGATTAACTACACGCAGGATGGGGGAAATGTAAGAGTCACCGTAGTGAACATTCAGAAGGCAGACGGGACGGAGAGTGTACGCTTTACCGTCAGTGATACAGGCATGGGGATTCCGCGCAAAGATCTGCCGCGTATCTTCGAACGCTTCTACCGGGTGGACAAAGCCCGTTCCAGAAGCTCCGGTGGAACCGGCCTGGGCTTGTCTATCGTGAAGCATCTGGTGGAGCTGCACCGCGGCTCGATTACGGTAGAGAGCGATCTGGGTATCGGCAGCTCCTTCATCCTTGAACTTCCGCTGCTGCAGGAGGAGAACGCGTAGCCTGCAACGGTTCAATTCTGGCAGGACATCCGTCTTAAGCCTGCGGATAGGGCGCATGTCCTGATTTGATTGTATGTCAGCAAAGGGGTAATATTAAATTCGTAATTTTACACCAAGTTAACATTGTGGTGCTATGATGTGCATGTATGCAGTTATGTAAAATTAATAACCTATGAAAAGACGGGGGAACCTATGGCACAACGATTGCTTGTCATTGAAGACGAACCGACACTGGCCCGGCTGCTGTCTTATAACCTGACGCAGGAAGGCTACGAAGTGACGGTGGAGGATCATGGAACGGCAGGATACGACCGTGCGACTAGAGAACCTTTTGACCTGATCGTACTGGATCTTATGCTGCCCGGCATGAACGGCATTGACATTCTGGATAAATTGCGTGGACAAGGCATACGCACACCGGTCATTGTGCTGACGGCCAAGAATGCTGAAGAAGATGTAGTCCGGGGGCTGAAATCGGGAGCGGATGATTACATAACCAAACCGTTTGGCGTCTCCGAATTACTGGCCCGTGTCAGTGCTGTCCTGCGCCGGATATCCGGCCTTGCCGAAGAGGCGCCACCGGAAACGGCGGTATCCGCATCGACCATTATCCTGGGACAGCTGGAAATCTACCCGGAACGTTACGAAGTCTCTCTGGGCGGACAGAGCATTAATCTGCGGCCGAAGGAATTTGAAGTTCTGCTGTATCTGGCCCGCAAGCCGGGTGTGGTTCTGACGCGCGATGATCTGATGAATGCGGTCTGGGGCTTCGATTATATCGGCGGCCAGCGTACCGTAGACGTTCATGTCAGCTCGCTGCGCAAGAAGCTTGAGCTTGATCCTGAATCCGTGCATATTGATTCCATCCGCGGCGTCGGCTATAAGCTGGTCGTGAACAAGAAGAGAACACCAGTCATTTGATATGGCGGTGTTCTTTTTCTGGTACACTTGTCCTGCTGATTTTTGATTTTACACTGCGTTAACAATTCTCTAGAGCTCTATTTACACTGAAAGCTTATCATGGGGAACGAAGATGATGAGAAGGAGACAATAGAAACTAATGAAATCCATCATTGACATAGAGAAACTTGATCTCTACTATGAGTCATTTCACGCGCTGAAGAATGTGGATCTGCAAATTCCGGAGAAACAGGTTACCGCTTTTATCGGTCCTTCCGGCTGCGGAAAGTCCACGCTGCTGCGTACCCTAAATCGAATGAACGACATGATTCCCGGAACACGCATTGAAGGAAAAGTAAACATCGGCGGTAAAAATATTTACAGCGACGAGATTGAAGTGGAAAGTCTGCGCAAGCAGGTGGGAATGGTATTCCAGCAGCCCAATCCTTTTCCAAAGTCGATTTATGACAATGTAGCTTACGGTCCGCGCCTCCATGGGGTGAAGGGCAAAGCCGAGCTTGATGTCATTGTGGAGCAAAGCCTGCGCCAATCCGCACTCTGGGAGGAAGTGAAGGATTTCCTCAAGAAATCTGCCCTCAGCCTGTCCGGCGGCCAGCAGCAGCGTCTCTGCATTGCCAGAGCCCTTGCCGTACAGCCCGATATTCTGCTTATGGACGAGGCAACCTCTGCGCTTGATCCGGTGTCCACGCTGAAGATCGAGGAACTGGTACAGGAGCTGCGCGATAAGTATACGATTGTAATGGTCACGCATAATATGCATCAGGCTGCCCGGGTATCGGGTCGTACCGTGTTTTTCCTGAACGGCGTCATCGTGGAGGCTCAGGATACGGAACTGCTGTTCTCGAATCCCAAAGACTCCCGCACAGAAGATTATATATCCGGCCGGTTCGGCTAAGCGGCAGAGGAATCCGTTCGCGGAAAGAAATCAGCGGTATAAGCTGAACTTAAGAATGCTTTACAGGTGATTCTTGAGTTCACTCTATATGACCATATGTTTTTGAGGAGGATCGTTTTCAATATGATTCGCAGAAAAGAATTCGATAAAGATCTGGAAGAACTGCGCAGTCTGCTGGAGCAGATGGGCGAGCATGTTACGGATGCGCTGGAAGGTGCAGTACTCGCTTTGCAGAATCTGGACACCGTGCGGGCACAGGAAATTGTTAAGAACGATTTGCGGCTGAATGCCATGGAGGACCGGATTATGGAGATCGGCTCACGGCTGATTATCACTCAGCAGCCGGTAGCGAAGGATCTGCGCCGCATTATTGTGGCCTTCAAAATTTCCAGTGACCTCGAGCGTATGGGCGATCTTGCACTGGATGTGGCCAAGGTAACCATGCGTATCCAGGGGCAGCAGCTGATTAAACCGCTTGTGGATATTCCGCGGATGGCCGAGATTGTTACCGTAATGATCTCAGAGGCGATTCAGTCCTATCTGGATGAGAACACCGATCTGGCCTACAAAATGGCTCAGGACGACGATCAGGTAGACGGGCTGTACAGCGCAATGATTAATGAACTGTACACTTACATGGTTCAGAAGCCTGAATCGGTTAATCAGGCTATGCTGCTCACGCTGGTCGGACGTTATATTGAGCGTATCGCCGATCATGCGACCAACATTGGCGAGAGCGTAGTGTATCTTGTAACGGGTAAACGTCCGGATTTGAATCAATAAAAGCATAGGGTACGACAGCAAGCCTTCATCCCCGGAGGCTTGCCTTTTTTGTTTTAAAGTGCTGTACGGTTGGAAATCCTGCTTAGAATGGCTCAAGCTGAAGACACGGTGTGAATCCGGCTTCATTCTGGGCGCTCAGGTTCTTTTTTATGCGGGGCATATGGTACTATATAAGAAGTAAGCAAGATTAAAGGCGAGGTGCTAGAGTGGACAAGCTGATACTGATCGATGGAAATAATATCATTTACCGGGCATTTTTCGCGATGCCTCCCCTGACGAATACAGCAGGACAGCAGACGAATGCAGTGTACGGTTTCACGACAATGCTGCTGCGTTTGATTGAAGAGCATAAGCCGAGTCATATGATTGTGGCCTTTGATGCGGGGAAGATTACCTTCCGGCATGAAGGGTATGAAGATTATAAAGGCGGTCGCCAAAAGACTCCGCCGGAGCTGTCCGAACAGTTCCCGCTGCTGAAGGAATTGCTGCAGGGATTAGGGGTGCCGCAGTTTGAGATCGGCGGCTATGAAGCCGACGATATTATCGGCACCATCTCCCGCGAGGCGGATGCCGCCGGGCGGCAGGTGATGATTGTGTCCGGGGATAAGGACATGCTGCAGCTGGCATCCGAGCATACAACCGTGGCGCTGGTCCGCAAGGGCGTTACGGAAGTAGAGCTGTACGGGCCGCAGCAGATCCGGGACAAATATGATCTTACCCCGGAGCAGATCATCGATCTGAAAGGGCTGATGGGCGATGCCAGTGACAATATTCCCGGTGTACCGGGTGTAGGAGAGAAGACGGCGCTTAAGCTGCTCCAGCAGTTCGGATCGGTGGAAGGCGTACTGGCCGGAACCGGTGAGCTGAAGGGTAAAATGAAAGAAAAGCTGGAGGAGCATGCTGACAGCGCCATTATGAGCAAGAAGCTGGCGACGATCTACCGCGAAGTGCCGCTTGCGCATGCCTGGGAGGATATGGTCTTCAGCGGAATCAATACGGATACGGCTGGCCCTGCACTGGCCAAGCTGGAATTCAAATCCCTGCTCGAACGTCTGTCGCTCAGCGCTTATTCGCATGCAGCTGACGGCAGCGGTTCAGATCCTGCAGAAGTGGAAGCAGCGGCGCTCAATATAACTATTGTTGACGAAGCAGGAATGGCGGACCTGATTGCTGCGTTGCCGAGTATCTCCGCGCTGCATGTGGAGTCGAACGGTGAGAATCCGCACCGTGCGGAGGTCATTGGCCTCGGGCTGTCTTCACCGGAGCAGCACTACTTCGTGCCGTTTGCCCTGCTGAAGAGCACCGCAGCGGCACCCCTGCGGGACTGGCTCGGCGACGACAAGGCGCCGAAGAGCGGGTATGACCTGCACCGTGCCGATCTGGCGCTGCATTGGCAGGGGATTGCTTTTGCCGGAGCCGCTAATGATGTCCAGCTTGCAGCTTATCTGCTTGACCCGACGGAAGCGAACCAGAACTTGAATGATCTCACAAGTAAATACGGGCTGCCCCGTTTATCGCCGGATGAAGATGTATTTGGCAAAGGGGCCAAATATAGAATACCGGAGCTTGAAATACTCGGAAATCATGTCGCCCGCAAGAGCGCAACTGTGCTTGGCATCGTGCAGAAGCAGCAGGAGGAACTGAAGGAGACGGCAATGACCGGACTGTTCCAGGATCTCGAAATGCCGTTGTCGAGGATTCTTGCCGATATGGAGAAGCAGGGCATTGCGGTCAACCGGGATGACCTTATTGAGCTTGGCAAGGAGTTTGAAGCGCAAATCTCCAGGCTCGTTGCGGAAATCTACTCGATTTGCGGAACAGAGTTCAATCTCAATTCACCGAAGCAGCTGGGGGAAATCCTGTTCGTGAAGCTCGGCCTGCCTGTCGTGAAGAAGACGAAGACCGGGTATTCTACCGATGCCGAGGTGCTGGAGAAGCTGGCTCCATACCATGACGCCGTGCGTCTGATCCTGCAATACCGCTCCATTGCCAAGCTGCAGTCCACCTATGTGGAAGGCCTGCTGAAGGAAATCTCGCCGGAGACCGGCAAGGTTCATACCTTCTACCGGCAGACGATTGCCGCAACGGGCCGCCTCAGCAGCCAGTTCCCGAACCTGCAGAATATTCCGATCCGGCTGGAAGAAGGCCGCAAGATCCGTAAGGTGTTCGTGCCTTCCGAACCGGGCTGGTCGATTCTGGCGGCGGATTACTCGCAGATCGAGCTGCGTGTACTGGCGCATATCTCCGGTGATGAGCGGATGAAGGAAGCTTTTGTAGAGAATATGGATATTCACACCAAGACGGCGATGGATGTATTCGGCGTTACAGCCGATATGGTAGACAGCAATATGCGCCGTTCCGCCAAGGCGGTTAACTTCGGAATTGTGTATGGCATCAGTGATTATGGTCTGTCACAGAACCTGAACATTCCGCGCAAGGAAGCAGCCCAGTTCATTGAGCAGTATTTCGAAGTGTTCAAAGGCGTCCGCCGCTATATGGATGACATTGTCGTAGAGGCCCGCAAGCAGGGGTATGTGACCACCTTGCTGGAGCGCCGGCGCTATCTGCCGGAGATTAATGCGAAGAACTTCAACCTGCGTTCCTTCGCCGAGCGTACAGCCATGAATACGCCGATCCAGGGAACAGCCGCCGATATTATCAAGCTGGCGATGGTTCACATGGATCAGGCGCTGTACGAGCGCGGACTGAAGAGCCGCATGCTGCTGCAGGTGCACGATGAGCTTGTGTTCGAGGTGCCGGAAGATGAACTGGAGCAGATGAAGCAATTGCTGCCGGAAGTGATGGCCGGGGCACTGAAGCTGTCTGTTCCACTGAAGGCCGAGGTAAGTTTTGGCAGTAACTGGTATGAAGCGAAATAGGCTCCCCGCATCTGCTGTATATCCGGTATAATGGAGTGGAGGTGAGCCATTATGCCGGAATTACCGGAAGTCGAAACAGTTAGAAGAACACTTAATGATTTAATTACAGGCAAGCAGATAGAGCATGTCACCGTCCGGCTGCCGCGGATTATTCAGCGCCCGGATGATATTCAGGCTTTTGCACATATGCTGGCAGGCCATAGCGTAGAAACGGTTGAGCGCAGAGGCAAGTTCCTGAGGTTCGTCTTCGATGGACTTGTGATGGTCTCCCATCTGAGGATGGAAGGCCGTTACGGGGTGTACCGGGAGGGCGAGCCGCTGGACAAGCATACTCATGTAATTTTCCATTTCACCGACGGTACGGAGCTGCGTTATACCGATGTGCGCCAGTTCGGAACGATGCATCTGTTCCAGCCGGGTGAGGATCTGCTGCTGAAGCCGCTGAACAAGCTGGGACAGGAACCGCTGGATGCTGATTTCACACTGGAGCGCTTCAAGCAGATTGTCTCGAAGAGAAGTACCAAAATCAAGCCGCTGCTGCTGAATCAGGAATATATCGTTGGTATCGGCAATATTTATGTGGATGAATCCCTGCACCGTGCCGGTATTCATCCGGAAGAAGCCGCAAACTCTCTCTCGGAGGACCATCTGGCCAGGCTGCATCATGCTATCGTTGCAACCTTGACAGAGGCGGTGAATGCGGGAGGCTCCTCAGTGAAATCGTATGTCAACGGCCAGGGAGAGAGCGGGAATTATCAGGATCAGCACCGCATATACGGACGCAAGGATCAGCCGTGTGCTACCTGCGGAACGTTGATTGAGAAAAGTGTTGTCGGCGGCCGGGGCACGCATTATTGTCCGAGCTGCCAGCCTGTACCGGTGCAGATAAGGTAAGTATTCAGCCGGGCTTATGTAGTGGAATTATAAGGAAATTCTAAGCGGTGTTGTCCATGCTCCATCAAAAGGCAGGCACTCACTGCCCGTCCCGCCCATATAATGTGTGAAGATTGCTGATTAAGGCGAACGGAACCCGGCTTGCAAGGCCGCCGGGTCCCGGTTCTTCACGGGAGGGATTGCGGGTGCTGAGCCCATTGTTGTCATTGCTGCTGCTTGCGTTTGCTCTTAGTTTGGACGGATTTGGTGTTGGCATTACATATGGACTGCGTAAAATGAAAATTCCTTTGCTCTCAATTATGATTATCTCGCTCTGTTCGGGGGTAGTCATTTGTGTGTCTATGCAGGTCGGCGTGCTGCTGGCCAAGGTGGTCTCACCGCATGCCGCTTCCAGTATCGGAGCGGTTATTCTGGTCTTGATGGGCTGCTGGTCGCTGTTCCAGATGCTGACGCAGAAAGAAAAGGAGCAGGGAGATTCAGGGCTGGGTGCCGGAGAAAGGGTGCCAGACCGGCAAGCTTTGCTGGAGACGGCTGCCACTGCCGCTGCATTGGAGGGGGAGGCTGAGCCGCAGAAGCCGGCTGTATTCTCTCTGGAGCTCCGGCATCTGGGAGTAGTCATTCAGATCCTCCGCACCCCGTCGTCCGCCGATATGGATGCTTCCGGAAGCATTTCTTCCATGGAAGCGATGGTTCTGGGTATTGCGTTGTCGCTGGATGCCTTCGGCGCCGGTCTGGGGGCTGCGCTGCTCGGGTTCAGCCCGGTGTCGACCTCGCTGATGATCGCATTGTTCAGCGGAACTTTTCTGCTGCTGGGGATGAAGACAGGACTGAGATTGTCAGGCAGCTACTGGATGAAGCATGCGGCTGTTCTGCCGGCGTTATTATTAATTGCAATGGGTATAATGAAGCTATTATGAGGTGAGTACATGATTATGGGCTTAACCGGAGGGATTGCTTCCGGGAAAAGCACCGTGTCCGCACTGTTTGTCGCCAAGGGAGCTGCTCTGGTGGATGCCGATGTCATCGCCAGGGAGGTTATGCTCCCCGGACATCCGGTGCTGGCCGGTGCTGTACAGGCTTTTGGAGAGTCGATTCTGCAGCCGGACGGAACACTGGACCGGAACAGGCTGGGTGAGATTGTTTTCCGGGATCCGGAGGCACTTCAAACCTTGAACAATCTGACGCATCCGGCGATCCGCACAGAAATTAAGGACCGTATGTATACGTTAGATCAGGAAGATCCGCAGCGGCTGGTCATAGTGGATATTCCGCTGCTCTACGAATCACAGCTGGACAATTTATTCGATCAGATCATTGTGGTCTATGTGCCACGCAGGGTCCAATTGGCCCGGCTCATGGCGCGCAACGGAATGAAGCTGGAACAAGCCGAGAACCGGCTGAAATCGCAGATGGACATTGAACTGAAGCGCAGGAAAGCCGACTATGTAATTGACAACAGCGGTGATCCCGGATCTACGGAGCGGCAGGTTGCCGGCCTGTGGGACAGGCTGGGCCTCTCATGATGAAGTGGCTGCGCAAAAAAAGAGTACTCCTGCTGCTATTTATCGGCTTCACAGCGATTCTGTTCCTGGGCACCAATTGGATGTCGTGGTTTTATCCGATACATTATAAAGATGAGATCCGCAAACACAGCCTTACTTATCAGATGGATCCGTTCCTTGTGGCTTCAATCATCCGGGTGGAGACCAATTTCAAGACCGGCCGCGAATCTAAAAAGGGTGCACTCGGACTGATGCAGCTGATGCCGGATACCGCCAAGTGGGCGCTGGAAAAGGCCAAGCTTCCCGATGTATCGCTCGAGCGGCTAAAAGAAGAGCCTTCTTCCAATATCGAACTGGGCACCTGGTATTTGTCTACGCTTTCGCGGCAGTTTGACGGCAACCGCACAGCGGTCATAGCCGCTTATAATGCCGGACCCGGCAAAGTACAGAGCTGGCTGGATGAAGGCAAGTGGGACGGAACAGAAGCGGCTGTGAAGGATATTCCGTTCGGAGAGACCCGCCATTATGTACAGCGTGTCATTTATTATTATGACCAATACACGGAGCTCTACAGTGAATTCTGA

Protein sequences of DBSCAN-SWA_3

>NZ_CP009285|2716326:2726578|2720925_2723598_+|WP_042211755.1|DBSCAN-SWA
MDKLILIDGNNIIYRAFFAMPPLTNTAGQQTNAVYGFTTMLLRLIEEHKPSHMIVAFDAGKITFRHEGYEDYKGGRQKTPPELSEQFPLLKELLQGLGVPQFEIGGYEADDIIGTISREADAAGRQVMIVSGDKDMLQLASEHTTVALVRKGVTEVELYGPQQIRDKYDLTPEQIIDLKGLMGDASDNIPGVPGVGEKTALKLLQQFGSVEGVLAGTGELKGKMKEKLEEHADSAIMSKKLATIYREVPLAHAWEDMVFSGINTDTAGPALAKLEFKSLLERLSLSAYSHAADGSGSDPAEVEAAALNITIVDEAGMADLIAALPSISALHVESNGENPHRAEVIGLGLSSPEQHYFVPFALLKSTAAAPLRDWLGDDKAPKSGYDLHRADLALHWQGIAFAGAANDVQLAAYLLDPTEANQNLNDLTSKYGLPRLSPDEDVFGKGAKYRIPELEILGNHVARKSATVLGIVQKQQEELKETAMTGLFQDLEMPLSRILADMEKQGIAVNRDDLIELGKEFEAQISRLVAEIYSICGTEFNLNSPKQLGEILFVKLGLPVVKKTKTGYSTDAEVLEKLAPYHDAVRLILQYRSIAKLQSTYVEGLLKEISPETGKVHTFYRQTIAATGRLSSQFPNLQNIPIRLEEGRKIRKVFVPSEPGWSILAADYSQIELRVLAHISGDERMKEAFVENMDIHTKTAMDVFGVTADMVDSNMRRSAKAVNFGIVYGISDYGLSQNLNIPRKEAAQFIEQYFEVFKGVRRYMDDIVVEARKQGYVTTLLERRRYLPEINAKNFNLRSFAERTAMNTPIQGTAADIIKLAMVHMDQALYERGLKSRMLLQVHDELVFEVPEDELEQMKQLLPEVMAGALKLSVPLKAEVSFGSNWYEAK
>NZ_CP009285|2716326:2726578|2726014_2726578_+|WP_042219247.1|DBSCAN-SWA
MKWLRKKRVLLLLFIGFTAILFLGTNWMSWFYPIHYKDEIRKHSLTYQMDPFLVASIIRVETNFKTGRESKKGALGLMQLMPDTAKWALEKAKLPDVSLERLKEEPSSNIELGTWYLSTLSRQFDGNRTAVIAAYNAGPGKVQSWLDEGKWDGTEAAVKDIPFGETRHYVQRVIYYYDQYTELYSEF
>NZ_CP009285|2716326:2726578|2724677_2725409_+|WP_042211757.1|DBSCAN-SWA
MLSPLLSLLLLAFALSLDGFGVGITYGLRKMKIPLLSIMIISLCSGVVICVSMQVGVLLAKVVSPHAASSIGAVILVLMGCWSLFQMLTQKEKEQGDSGLGAGERVPDRQALLETAATAAALEGEAEPQKPAVFSLELRHLGVVIQILRTPSSADMDASGSISSMEAMVLGIALSLDAFGAGLGAALLGFSPVSTSLMIALFSGTFLLLGMKTGLRLSGSYWMKHAAVLPALLLIAMGIMKLL
>NZ_CP009285|2716326:2726578|2716326_2718120_+|WP_042211752.1|DBSCAN-SWA
MKPFRVRLTFILMALIGISMTGAGITMAQLFKDSHISVLEENMSREINLLSGTFTFKDIRSPDAMDYYTDQARKISTLTGSRITFITKEGRVIGDSERNPLEMDNHSTREEELIAAKEGIGRAIRYSDTLDREMLYVAGAVVSDQGFDGYIRLSMGLDAVTEGLNRAWMIMAGGLVLLFIAATFVSYKVASSMTSPLEQITRVARRITDLDYDARVPMKRKDEIGQLATAINAMADSLQAQLKTIRDNEDLLQSVLDNMTGGIVMINAEGEIALLNRAAERLLDVKNSEMTGHSYKEIKHHYELTRLIEEGVSAGEPVHEERIIYNPVERIVRLDGVPMIQDGSTRGMLFLLQEVTEIRRLEKMRSEFVANVSHELKTPVAAVKGFAETLLGGGVTDEKTARSFLQIIYDENERLNRLIGDILELSKIESKRVQLDCSPVHLIEFFDSVLETLSKVAEKKKITLSSDVPPELFIEGDEDKLRQIFMNLLSNAINYTQDGGNVRVTVVNIQKADGTESVRFTVSDTGMGIPRKDLPRIFERFYRVDKARSRSSGGTGLGLSIVKHLVELHRGSITVESDLGIGSSFILELPLLQEENA
>NZ_CP009285|2716326:2726578|2718312_2719041_+|WP_039304977.1|DBSCAN-SWA
MAQRLLVIEDEPTLARLLSYNLTQEGYEVTVEDHGTAGYDRATREPFDLIVLDLMLPGMNGIDILDKLRGQGIRTPVIVLTAKNAEEDVVRGLKSGADDYITKPFGVSELLARVSAVLRRISGLAEEAPPETAVSASTIILGQLEIYPERYEVSLGGQSINLRPKEFEVLLYLARKPGVVLTRDDLMNAVWGFDYIGGQRTVDVHVSSLRKKLELDPESVHIDSIRGVGYKLVVNKKRTPVI
>NZ_CP009285|2716326:2726578|2723649_2724492_+|WP_042211756.1|DBSCAN-SWA
MPELPEVETVRRTLNDLITGKQIEHVTVRLPRIIQRPDDIQAFAHMLAGHSVETVERRGKFLRFVFDGLVMVSHLRMEGRYGVYREGEPLDKHTHVIFHFTDGTELRYTDVRQFGTMHLFQPGEDLLLKPLNKLGQEPLDADFTLERFKQIVSKRSTKIKPLLLNQEYIVGIGNIYVDESLHRAGIHPEEAANSLSEDHLARLHHAIVATLTEAVNAGGSSVKSYVNGQGESGNYQDQHRIYGRKDQPCATCGTLIEKSVVGGRGTHYCPSCQPVPVQIR
>NZ_CP009285|2716326:2726578|2725418_2726015_+|WP_042211758.1|DBSCAN-SWA
MIMGLTGGIASGKSTVSALFVAKGAALVDADVIAREVMLPGHPVLAGAVQAFGESILQPDGTLDRNRLGEIVFRDPEALQTLNNLTHPAIRTEIKDRMYTLDQEDPQRLVIVDIPLLYESQLDNLFDQIIVVYVPRRVQLARLMARNGMKLEQAENRLKSQMDIELKRRKADYVIDNSGDPGSTERQVAGLWDRLGLS
>NZ_CP009285|2716326:2726578|2720059_2720719_+|WP_042211754.1|DBSCAN-SWA
MIRRKEFDKDLEELRSLLEQMGEHVTDALEGAVLALQNLDTVRAQEIVKNDLRLNAMEDRIMEIGSRLIITQQPVAKDLRRIIVAFKISSDLERMGDLALDVAKVTMRIQGQQLIKPLVDIPRMAEIVTVMISEAIQSYLDENTDLAYKMAQDDDQVDGLYSAMINELYTYMVQKPESVNQAMLLTLVGRYIERIADHATNIGESVVYLVTGKRPDLNQ
>NZ_CP009285|2716326:2726578|2719180_2719936_+|WP_042211753.1|DBSCAN-SWA
MKSIIDIEKLDLYYESFHALKNVDLQIPEKQVTAFIGPSGCGKSTLLRTLNRMNDMIPGTRIEGKVNIGGKNIYSDEIEVESLRKQVGMVFQQPNPFPKSIYDNVAYGPRLHGVKGKAELDVIVEQSLRQSALWEEVKDFLKKSALSLSGGQQQRLCIARALAVQPDILLMDEATSALDPVSTLKIEELVQELRDKYTIVMVTHNMHQAARVSGRTVFFLNGVIVEAQDTELLFSNPKDSRTEDYISGRFG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042211752.1|2716326_2718120_+	HAMP domain-containing protein	W8CYF6	Bacillus_phage	9.3e-39	33.5
WP_039304977.1|2718312_2719041_+	response regulator transcription factor	W8CYM9	Bacillus_phage	1.0e-36	35.2
WP_042211753.1|2719180_2719936_+	phosphate ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	2.1e-16	33.5
WP_042211754.1|2720059_2720719_+	phosphate signaling complex protein PhoU	NA	NA	NA	NA
WP_042211755.1|2720925_2723598_+	DNA polymerase I	A0A068EMS7	Bacillus_phage	1.1e-46	32.3
WP_042211756.1|2723649_2724492_+	DNA-formamidopyrimidine glycosylase	A0A127AWE5	Bacillus_phage	1.6e-20	28.4
WP_042211757.1|2724677_2725409_+	manganese efflux pump	NA	NA	NA	NA
WP_042211758.1|2725418_2726015_+	dephospho-CoA kinase	NA	NA	NA	NA
WP_042219247.1|2726014_2726578_+	lytic transglycosylase domain-containing protein	A0A0H3V0Q1	Geobacillus_virus	1.3e-15	38.4

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_CP009285|4662117:4669634|DBSCAN-SWA
TCTATACAGTCTGAGCAGACCACTGCTCTACATTCCATACCTTCGTTACCCAATCCTCATAGAATTCCGGTTCATGGGAGACAAGCAGAATCGTCCCTTTGTATTCCTGCAGCGCCCGTTTGAGCTCTGCCTTGGCAACAATATCAAGGTGATTCGTAGGCTCATCGAACAGAATCCAGTTGCTCTCGCGCATCAGCAGCTTACACAGACGTACTTTGGCCTGCTCGCCCCCGCTCAGCATGCTAAGCGGACGGGTAATATGTTCATTCTTCAGCCCGCAGCGCGCCAGATGGCCACGCACTTCATTCTGGGTGAGACTGGAGAATTCATTCCACACATCTTCAATCGGGGTAATATTCTCCGCCTTCATTTCCTGCTGGAAGTACGCCGAATTCAGGTAATCCCCCAGATAGGTTTTGCCGCTGTAGGTCGGGATTACGCCCAGAATCGTTTTGAGTAGTGTGGATTTGCCGACACCATTGTACCCGACAATTGCAATCTTCTCCCCGCGTTCAATCATCATATTCAGCTTGCTTGGCAGCAGCGGACGATCATAACCGATCTCAAAGTCAACGCCTTCGAACACGGTCTTCCCGCTGGCCCGGCTCTCTTTGAACTGGAAGGTCGGCTTCATCGCCTCTTCCGGACGGTCAATCCGTTCCAGGCGTCCAAGCTGCTTCTCACGGCTCTTGGCCCGGCCCGATGTGGAAGCACGCGCTTTATTGCGCTGGATGAAGTCTTCCTGCTTTTTGATGAAATCCTGCTGCTTCTCATAGGCATCAATGTGCTGGGCCTTGTTCATACCCGCCATTTCCAGAAATTTCTCGTAGTTTGCCGTATAGCGGGTCAGCTTCGAGAACTCCAGATGATAGATCACATCCACGATTTTGTTCATAAATTCCGTATCATGGGAGATCAGCATGAAGGCATACGGATAATTCTTCAGATAATTGGTCAGCCAGTCAATATGCTCCACATCCAGATAGTTGGTAGGCTCATCGAGCAGCAGCACGTTCGGTTTCTCCAGCAGCAGCTTGGCCAGCAGAACCTTAGTCCGCTGGCCCCCGCTCAGGCTGGTTACGTCACGGTCCAGACCGATTGCCGACAGGCCGAGGCCGCCTGCCATATCCTCCACCTTCACATCAATCATATAAAAGTCGCCGATGTCCAGCTGTTCCTGAATCGTGCCCATTTGATCCAGCAGCGTTTCCAGCTCTTCAGGAGTGGCGTCACCCATTTTATCAGTGATGGCCAGCATTTCAGCCTCCAGCTCCAGCAGCGGCAGGAAGGCATCTTTAAGCACATCTCGTACTGTTTTGCCTGCCGTAAGCTGGGTGTGCTGATCAAGATATCCGTAACGGACACGCGGAGTCCACTCCAGCTTGCCGCTGTCCTTCAACAATTTACCGGTCAAAATATTCATCAGCGTCGACTTGCCCACGCCGTTAGCTCCAACAATTCCTACATGCTCTCCATCCAGCAGGCGGAAAGATACATCCTTGAACAATACCCGGTCCCCAAAGTTGTGGGAAACGTCTTCTACAGTAAGTAAACTCATAAATTCTCCGCAAGCTCCTGTCTATATTATAAATATTACGAAACGGGTTAAGCACATACATCACTCCATTCTAGCACACCTATGTCCTGCGCCGAAATAGAAAATAAGCCTAATTCCTGCAAAACACGCAGAAAAAGTTGTGATTTCAATGTTTTTTCTGAAATATTCCATTATTTTTTGCAGAAAATCGTCTGCCTGAAGCCAGCCCCAGCATCTCTCCAACCGCTTGACCCAGCTTTCCTTTGGGCTGAAACGGGTCCCGCTGTAGCGGCAGACTGCATACGCTGGCCTTCCCCAAAGCAGAAGCCAGAAGCGCTGCCGCAGAGCCGCCCGCCAGCGGCAGACAGATCCGCCAGTCCTGCTGAGGGTTTAGCCCGCTGCGACGCAGCCAGTGCAGAGTATCCTCCAGGCGCCAATCTGCCCCGGAAGCGACCAGCACCGGCCTGTCGCAGGCCGTGAAGGAGGCCAGCGCCCCTTCATAACCACCTATCCCCAGATCCAGTACTATGAAGGAATACCTCTCATCCGTCCGCTCAGGAAATCCGTCAGCAGGCGCAAGCTTCCAGAAATCCACGTTGTTCCAGGTAAAGGGTGACTCCGGCAACATCCTACCATGGATGCCGCTTAATTCAGGCACTTCCACCATTCCTTTAATACGATTAAATACTTGCGTACCTGGAGCGCATTCCACCCAGGCTGTGAGACCTGCCTGTGACAAATAATGGCTCACAGCCAGTGAAGTATGCGTCGTCCCAAGTCCCGGGCCTACACCCAGCACAGCCACTACGATAGTCTCCAGGGACTGTATTCCAGCAGAACGGACTCGTAAATCCGGCTTGTGCCTCGGCGCTGACGGCAGCTCAGCGGCTTCAAGCAGTTCAAGGGCTGACAGCACCTCCTCAGCACTGCCGTACCGCTCCTCCGGATGATGACGTAATAGACGCCGGATCACCGGAATCAGCCGGTCCGGAATGCTGCCGTGCAGCTTCCGTTCCATGCCCGGCTGCCAGCTGCTGAATTGTCCGCCGGAAGCCATGTACAGCAGCAGCGCGCCCAGGCCGTACAGATCAGACAGCGGACTGCTCTGCAAGCCGCCATATTGCTCCGGGGCAGCAAATCCGGCGGTGCCCAGCTTCTCCGTGTCCTCATCTGAACCGTTTCTCTGCTTACGCGCAATACCGAAATCAATCAGTTTCAGCTCATGTTGTCCGGTCAGCATAATATTGGATGGCTTGAGGTCACGGTAGACGATCGGCGGACGATGACTATGCAGATATTGCAGGACCTCCAGCAGCTGCCTGGCATAGCGGACGATTTGCATTCCCGGGAGGGCAGCCGGATGGTCAATCATGTATTGATGAAGTGTCACCCCTTCAATGTAATCCATTACCAGATAACTATAGCCGTCACGGTCCGGCGGGAAGAAGTCGGCAATCCGCGGCAGCTTAGGATGATTTAGTGAGATCAGCAGCTCCGCCTCCGCCTGGATGGTTCCAACGCTACGTATCCCTCCTTCCCGCATCACACTTTCCTTAACTGCCCAGTACTTCCCCGGCAGCCGCAAATCCTCTGCCAGATACACCTGACTCATCCCTCCTTTACCAATAATTCCGTTGATACAGTAACGTCCTCCAATAATTTGACCGGTTGTCAGTTTACCTGCGAAATTCATCTTTTCTCCTCCTCATTTTCACAACAAAAAAAAGGGAAAGCAACCGCCATCCGCACCTTAAACCGGCATGCAGCCGGCGGTGCAGATAACGGGATGCTTTCCCTTTATCCATGAATCCAAATTAATATTTAATCATATAAAGTGTTATTTCATCGCGGTTGTGAAACAGCTGCTTCGCGCGCTGAATCTGCATCCGCTCACCTTCGAACATGGCAATAATCTCTTTGATCATCGCCAGCGGCTTCTTATGCATCAGCTTCACCGTGACAATGGCCGTACCGCCCGGAGTCAGACTATGGAGCAGTCCGGTAACCAGCTTGGCCATCAGCTTGGGGCTCCAGCTCATGTCGCAGACCAGCAGGTCAAATTCATTCTCGCGGAATTTGACCTCTCCGGCATTTTTGCGCAGAATTTTGAGTCCCGGATGATTGCGCAGCGATTCATGCATCAGCGCCGGATCCACAGCAGTTACCTTCAGGCCCCGTTCCAGCAGGAACGAGGTCCAACCGCCCGGGGAAGCGCCGATATCTACCGCATTCCTGAAGCTGTAGAACGGAATGGCGAATTCCTTCTCCGCCTCCATAAGCTTGAACTTAGCCCGTGAGATCTGACCGTCCTCCTTGCGGAAGCGGATCATCCCGCCGTTCCAGCTGGAGAGGTTCTCTTCCGGCCGGGATACACCGGCATATAGCGCTTCTCCGTCTGCATAGACGGACACCACCCATGCAGCGTCCTGCACGGTGAATTCGGCACCCAGACTGTCAAGCCGGGCTTGCAGCCACTCGCGCAGCTCTCCCGGGCTGTCTTCCCAGAAGGAAGTGCTGCCCTTGCGGACATGCAGCGAGACCTTCTCACCTTCCAGCTCTGTCCGGCGGCTTAAGTATACGGCCAGCCTTTCCATAGCAGACATATCGCCTGTGTCCTGGAACTGTACGGGCTGGATATGCCGCAGGAAGATCGGCAAGTTCTGTGCCAGCATCCGCGATACCTCTTCGGGCTCCGCTTCCAGCGTTGCCAGGAACACTTCCCCCGGCAGCAGCAAGGTACTCTTCACCGCTCCGAACAGGCGGCGCAGCTCCTCTTGTGCATAGGGAGCAAAGCCGTGATTCGCGGTGCAGATGTATCTTGAAATTATTTTTTCGTCAGGAGCTATGTTGGGCTCGAGGGGTTCTTGCGTAAAATCATTCAATTCGATGTGCCTCCAGGTCTTATTTTAATCCAGGGACGGCCGCTATCCCATTCAACATCAACGGGTATATCGAAAGTGTCCATCAGCATTTCCCTGGTCAGCACTTCTTCCTTGGGACCGGCTCCTGCCAGCTTCCCGTCACGGATCAGCGCCACATGGGTGAAGAGCGGTACAATCTCCTCCACATGATGTGTTACATACACTACAGCAACATTGTGCTGCTTAAGCTTGTCTATCTCAGCCAGCATCTTCTCGCGTTCAAATAGATCCAGACCGGCACAAGGCTCGTCCATAATCAGCAGCTTGGGCTCGGCCATCAGGCAGCGTGCCAGCATCGCTTTCTTGCGCTCTCCCTGGGACAGGGTACCAAACGGATGATAAGCCAGTTCGCTAAGATTCATATCGTCCAGCAGCTTCAGCGCCTGATCCTGTACGCTTTGCGGAATGGCCTGATAGAAACGCAGGTAAGCATACGCACCAGTTGCAACAACTTCCCATACGGGATCGGTGAGCGACAGCTTTTCCATCAGGGAAGGACCGATATAGCCGATCTCCTTGCGCACCTCGCGTAAATCACACTGTCCGAATTTGTAACCCAGTACTTCAACGGAACCTTTACTTGGAAACAGGTATCCGGTCATCATTTCCAGCAAAGTGGTTTTACCGGAGCCGTTACGACCGAGAATTACCCAGTTCTCGCCTTGCTTCATTTCCAGAGACACATCATCAAGAATCAGGCTTTGTTCCCTGCGCAGGGAAAGATGTTGTAAAGAAATCATTATGAGGTCACTCTCCTTATGTAATCCAGTACCCGTTCTACCGAGCCCATTGAATACAAGATTTCCGGTTCAGCGCTGCGGTCCGCCGGCACTACCATCAGTGCAGGCACACTGGATATACGATACGCGTTTACAAGTCCGGGCAGCATATTTACGTTTCCTTCTGCAATCAGAAGTACTGGCGGAAGCAGATGCTGCGCAACCTCCAGCATACGCCTTGCGGCCTTGCAGGTTCCGCACAGCGGGGTATACAAGAACACTACGAGAGGTTCTCCCGGTCTTCCGAGCAGCTCCATCAGCTCGTCCTGATTCATGTCCTTCATCCGGCCGCACCTGTAGCAATTTCCTGCAGCCTCTCAAACCCAAGCGGGCCGTTATGAAGCAGTGTACTTGCAGGTACGGCCGGATACAAGGTTTCGTACATTTCCTTGCGGCCCTCAAGGCTGGAGGTATGCAGATAGATTTCCCGCGGGAATAATCCTTCGAGTACCATCCTTTTGGCCACTTCACCGCCGCTGAAATCATCCGGACCCATATCATAATCAAGCGACAGAACATCAATCGGGCCGCTGCGCAGCATCAGCAGACATTCTCCGGTGGTTCTGGCCAATGCAAAACCGGAAGGACGTCTTCTCATATCGTCCATATATATATTCATCACGATTCATCCTCCGCTTCAAACCAATGCCTGACTTCAGCAATTTCCGCCCTGTGAGTGCCGTCAGGACCTTTTTCCGTTTCCATCGCAACCGCTGCCACCTTGCGCAGGGGAACAGAGGTCAGCAGCTCCCTGAGCGCCTTCCCGCCAATATGGCCTTGCCCGATCTGGGCATGTCTGTCCCGCCTGGAGCCGCAGGGGAACAGGGAGTCGTTCAGATGTACGGCAGCAAGATGCGGCCAGTAGCCGAGTGCTTCTCCCCTCTGCAGCAGCTCATCAGTATGCTGAGGATTCCAAATCCCTGATGCGAAGGCATGACAGGTATCGAAGCAGAAGCCGATTTTGTCCGGATAGCGGCTCAGCTCACGGACTTTGACCAGCTCCTCCAGCGTCATGCCTTCATGGCCGTGATTGCCAGCCATATTCTCGATCAGCAGCTTTGTCTGGCCTTCCCATCCTGACAGGGTGTCATTTATACATTGTATAATATTTTGATAACCTTGTAATGGCTCCATTCCGGCAAAATGGCCGAAATGCACCACAATGCCCAGGGAACCGCAAGCCTCGGCGATCTCCAGATCATTGCGCAGCGAAGCAGCCATAATGGCTCTGCCTGCGGGATCTGCGGCCAGATTGGTAGGATAAGGGGTATGGGCAATCGAGACCATCCCCTGATCCCGGCAATAATCGGCACAGCTGCGCGCATCCCTGTAGTCCACCGGCTTAAGCTTCAGACTCCGCGGATTCTTCGGAAAATATTGAAAACATGACGCACCGCTCTCCCTGGCGAACCGGGCAGCCTGCCCGTATCCGCCGCGTATGCTGACATGTGCCCCTATACCGGGATTAAGCGTCATGCTGGCAATCGGGGCAATAGAATACCTTGCGTCCGGACTGCTCTGTCTTGAGTATCGTTCCCCCGCCGCGCAGGCAGGGTTCGCCGCCGCGGTCGTACACTTTACAAGCATTGTTGTAAGAGCCGGTAACCGTATCTCCGGTCATGAAAGGCATTTCCATATAACCGCCAATCTCGGTTGCCTCCGTCAATACCTTGCGCACACTGTCATACAGCCGGGTCACTGCCTCCGGTGACAGATTCTGAACGAGCGTAGAAGGCAGAAGTCTTGCTTCAAAGGCAATCTCGTCGGCATAACAATTGCCGATTCCGGCCATAACATGCTGGTTGACCAGCAGACTCTTCAGCGCACCGCGGCGTCCTTTGAGCAGTCCGGCGAAGCGTTCAGCCGTCATCCTCCGGTCCAGCAGCTCCGGTCCAAGCTTACCCATTGCCGCTTCGCTTTCCTTAACAGACAGGAGATGCAGATATCCCAGGCGCAGGCCCATGAAATAGAGGATATGCTCTCCAAAAGCCAGTTCAACCTGAGTAGTCCGGTCCGGACGCTCTTGCTCTGTACCATAGAACAAAAGTCCGCCTAACATCAGATGAAGCAGCAGTCTTCTTCCGTCATGCAGATGGAAGAGGATATGCTTGGCACGGCGCTCTACGAACACAATACGCGCGCCAACCAGACCGTTCACGAAATCCGCTGTCTCCATATTGATTGTTTTTTCTCTGTTTACGGTTACCCCCGTAATTGGAACATTTATTAGATGCTGGCTCAGCAGCTTTCTGTAATTCTCCATTTCCGGCAATTCCGGCAT

Protein sequences of DBSCAN-SWA_4

>NZ_CP009285|4662117:4669634|4666531_4667314_-|WP_042214469.1|DBSCAN-SWA
MISLQHLSLRREQSLILDDVSLEMKQGENWVILGRNGSGKTTLLEMMTGYLFPSKGSVEVLGYKFGQCDLREVRKEIGYIGPSLMEKLSLTDPVWEVVATGAYAYLRFYQAIPQSVQDQALKLLDDMNLSELAYHPFGTLSQGERKKAMLARCLMAEPKLLIMDEPCAGLDLFEREKMLAEIDKLKQHNVAVVYVTHHVEEIVPLFTHVALIRDGKLAGAGPKEEVLTREMLMDTFDIPVDVEWDSGRPWIKIRPGGTSN
>NZ_CP009285|4662117:4669634|4668818_4669634_-|WP_042214479.1|DBSCAN-SWA
MPELPEMENYRKLLSQHLINVPITGVTVNREKTINMETADFVNGLVGARIVFVERRAKHILFHLHDGRRLLLHLMLGGLLFYGTEQERPDRTTQVELAFGEHILYFMGLRLGYLHLLSVKESEAAMGKLGPELLDRRMTAERFAGLLKGRRGALKSLLVNQHVMAGIGNCYADEIAFEARLLPSTLVQNLSPEAVTRLYDSVRKVLTEATEIGGYMEMPFMTGDTVTGSYNNACKVYDRGGEPCLRGGGTILKTEQSGRKVFYCPDCQHDA
>NZ_CP009285|4662117:4669634|4667633_4667975_-|WP_042214473.1|DBSCAN-SWA
MMNIYMDDMRRRPSGFALARTTGECLLMLRSGPIDVLSLDYDMGPDDFSGGEVAKRMVLEGLFPREIYLHTSSLEGRKEMYETLYPAVPASTLLHNGPLGFERLQEIATGAAG
>NZ_CP009285|4662117:4669634|4665467_4666499_-|WP_052429811.1|DBSCAN-SWA
MAPDEKIISRYICTANHGFAPYAQEELRRLFGAVKSTLLLPGEVFLATLEAEPEEVSRMLAQNLPIFLRHIQPVQFQDTGDMSAMERLAVYLSRRTELEGEKVSLHVRKGSTSFWEDSPGELREWLQARLDSLGAEFTVQDAAWVVSVYADGEALYAGVSRPEENLSSWNGGMIRFRKEDGQISRAKFKLMEAEKEFAIPFYSFRNAVDIGASPGGWTSFLLERGLKVTAVDPALMHESLRNHPGLKILRKNAGEVKFRENEFDLLVCDMSWSPKLMAKLVTGLLHSLTPGGTAIVTVKLMHKKPLAMIKEIIAMFEGERMQIQRAKQLFHNRDEITLYMIKY
>NZ_CP009285|4662117:4669634|4667971_4668829_-|WP_042214476.1|DBSCAN-SWA
MTLNPGIGAHVSIRGGYGQAARFARESGASCFQYFPKNPRSLKLKPVDYRDARSCADYCRDQGMVSIAHTPYPTNLAADPAGRAIMAASLRNDLEIAEACGSLGIVVHFGHFAGMEPLQGYQNIIQCINDTLSGWEGQTKLLIENMAGNHGHEGMTLEELVKVRELSRYPDKIGFCFDTCHAFASGIWNPQHTDELLQRGEALGYWPHLAAVHLNDSLFPCGSRRDRHAQIGQGHIGGKALRELLTSVPLRKVAAVAMETEKGPDGTHRAEIAEVRHWFEAEDES
>NZ_CP009285|4662117:4669634|4667313_4667637_-|WP_042214472.1|DBSCAN-SWA
MKDMNQDELMELLGRPGEPLVVFLYTPLCGTCKAARRMLEVAQHLLPPVLLIAEGNVNMLPGLVNAYRISSVPALMVVPADRSAEPEILYSMGSVERVLDYIRRVTS
>NZ_CP009285|4662117:4669634|4663819_4665346_-|WP_042214465.1|DBSCAN-SWA
MNFAGKLTTGQIIGGRYCINGIIGKGGMSQVYLAEDLRLPGKYWAVKESVMREGGIRSVGTIQAEAELLISLNHPKLPRIADFFPPDRDGYSYLVMDYIEGVTLHQYMIDHPAALPGMQIVRYARQLLEVLQYLHSHRPPIVYRDLKPSNIMLTGQHELKLIDFGIARKQRNGSDEDTEKLGTAGFAAPEQYGGLQSSPLSDLYGLGALLLYMASGGQFSSWQPGMERKLHGSIPDRLIPVIRRLLRHHPEERYGSAEEVLSALELLEAAELPSAPRHKPDLRVRSAGIQSLETIVVAVLGVGPGLGTTHTSLAVSHYLSQAGLTAWVECAPGTQVFNRIKGMVEVPELSGIHGRMLPESPFTWNNVDFWKLAPADGFPERTDERYSFIVLDLGIGGYEGALASFTACDRPVLVASGADWRLEDTLHWLRRSGLNPQQDWRICLPLAGGSAAALLASALGKASVCSLPLQRDPFQPKGKLGQAVGEMLGLASGRRFSAKNNGIFQKKH
>NZ_CP009285|4662117:4669634|4662117_4663674_-|WP_042214463.1|DBSCAN-SWA
MSLLTVEDVSHNFGDRVLFKDVSFRLLDGEHVGIVGANGVGKSTLMNILTGKLLKDSGKLEWTPRVRYGYLDQHTQLTAGKTVRDVLKDAFLPLLELEAEMLAITDKMGDATPEELETLLDQMGTIQEQLDIGDFYMIDVKVEDMAGGLGLSAIGLDRDVTSLSGGQRTKVLLAKLLLEKPNVLLLDEPTNYLDVEHIDWLTNYLKNYPYAFMLISHDTEFMNKIVDVIYHLEFSKLTRYTANYEKFLEMAGMNKAQHIDAYEKQQDFIKKQEDFIQRNKARASTSGRAKSREKQLGRLERIDRPEEAMKPTFQFKESRASGKTVFEGVDFEIGYDRPLLPSKLNMMIERGEKIAIVGYNGVGKSTLLKTILGVIPTYSGKTYLGDYLNSAYFQQEMKAENITPIEDVWNEFSSLTQNEVRGHLARCGLKNEHITRPLSMLSGGEQAKVRLCKLLMRESNWILFDEPTNHLDIVAKAELKRALQEYKGTILLVSHEPEFYEDWVTKVWNVEQWSAQTV

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042214463.1|4662117_4663674_-	ABC-F family ATP-binding cassette domain-containing protein	A0A2K9L3Z8	Tupanvirus	4.6e-50	28.3
WP_042214465.1|4663819_4665346_-	serine/threonine protein kinase	A0A1V0SGY7	Hokovirus	1.6e-15	27.4
WP_052429811.1|4665467_4666499_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_042214469.1|4666531_4667314_-	ATP-binding cassette domain-containing protein	F2Y302	Organic_Lake_phycodnavirus	7.2e-12	29.3
WP_042214472.1|4667313_4667637_-	thioredoxin family protein	NA	NA	NA	NA
WP_042214473.1|4667633_4667975_-	hypothetical protein	A0A109QIR8	Bacillus_phage	7.0e-12	41.2
WP_042214476.1|4667971_4668829_-	deoxyribonuclease IV	A0A2P1EJ83	Megavirus	1.5e-15	25.2
WP_042214479.1|4668818_4669634_-	Fpg/Nei family DNA glycosylase	A0A127AWE5	Bacillus_phage	1.8e-13	25.0

Sequences of DBSCAN-SWA_5

Nucleotide sequences of DBSCAN-SWA_5

>NZ_CP009285|5329911:5337936|DBSCAN-SWA
ACTATCTCTGATCTTCGCCGCTCTGGAACAAGGCTCGCAGCGCGCTGCCGAATGCCTGCAGCCAGTTATCCGCCGGATAAGCAGTTCCTCCCGCAGGACTGTATTTCTTCTCGTAGGCGGATGTTTCCGGCGGCAGCTGGCTTGGCGTATACACGGGAACCCGGCCGATTTCCTTGCCGCCAAGCTGCATTATAATCACACCCTTCAGCCCGAAGCTGCTGGCGTTGGCGCTGCTACTGGCGCCGGTGCCGCTATTGCCACGCGCATCCGCCACCCCTGCACTCTTCTCCTCACTAAGTACCAGCTTCGTAATTAGCCTTGCCTCTTCCCCTTGTCCGAGCGGATAGGCGAAGTCCTTGCCGGTAACCAGGCTGTAGCCGCTGACAGCTTCTCCGCGTTCCACTAAGGTCTTGAGCGGATAGTGGTTGAAGCCGAAATCCAGCAGCGCCGAATGGTCATTCCAGTCATTGCCGTCATTGAGCGTAACAGCGACAAGCTGCTGGCCGTTTCTGGTGGCAGAGCTGACCAGGCAGCGGAGCGCTTTTTTGGTATAACCCGTCTTCACACCGTCCGCCCCTTCGTAGAGGCGCAGCATTTTATTTTTATTACTCCATTTGTAATCCCATTTCTCATACGGATTGTCCGCCGTCTTCTCTTTGGTGGCCACAATCTCCTTGAACACGGGGTTATGCATCGCATAAGCAGTCAATACAGCCAAATCATTTGCGCTGGAATAATGCCCTTCGGCATCAAGCCCGTGCGGGTTGGCAAAATGCGTATGGGTTAAGTTAAGCGCCTCCGCCTTGGCATTCATCAGATAGACAAAGCCCTGCTCGGAACCTCCGACATGCTCAGCAATTGCGGTTGCCGCATCGTTGCCCGAACGCAGCATTAATCCATACAGCATATCCTCCAGCGTCATTTCTTCGCCCTGCTTCAGATACAGTGAAGAACCTTCCTTGGCAAAGGCATTTTTGCCGACCTTGACCTTTGACGTCAAATTACCGTTTTCTATCGCTACTAGTGCAGTCATTATTTTGGTCAAACTGGCAATCAGCATCGGCTCATCACCGCGGCTGCTGTATAGAAGTCTTCCCGACTCCACATCAATCAGCGCCGCCGCTCTGGCATGAGTAGAAATCGAACTGTTCTCTGCCCGGATAGAAGACAATGGCACCAGTGCAAGCAGCAGTAAACACAAAATTAAGGAAATCAACGATTTACGGGTTAATGTCTTCATGTTCATCCTCCGGCTTCTTATCAGGTCTAGGGCAGCGGTTCTTCCGTCTTGCCTGGTTGTACAAGTGTATGCGGTACGGGGGACTGGTATGTCCCATCCGCTTCTGTCCGTCAAAAAAGGGATATCACCTTTGAAAGGCGATACCCCCGCTTATACATAACCGTCAGCTTCCTGGCGGTGTGTTAATGTGCCGACGAGTGAGTGGTTGGCTCAGTTTTGACTACAGTTTTGGTCACCTCGGCAACATGGGCATCATTCCCCACAGGAATGCCGCCTGGCTGGAACATATTCTGGATTTTATCGATCAGGTTAGGTGTGGCATCAATAATTTTCTCGAACAGATGGGTTTGATTGTCAAGCGGCACAATATGTACCCCATCCCTGCCCACTACCAGAAAAGCGATTGGACGTATGGATACACCGCCCCCGCTACCGCCTCCGAAGGGAAGCATTTTGACTCCGGTTCCGCTGCCGTTCACGCCCGGAGCATCGTCTTCCACCCGGAAGTCACTGCCGCCTGCGGCAAAACCGAACGCAACCTTACTGATCGGCAGAATGATACTGCCATCCGGCGTTTCTACAGGATCACCGACAATCGTATTTACATCAACCATGCCTTTGATATTTTCCATAGCCGTCTGCATGAGACCTTGAATAGGATGATCTGACATTGTTTTTCTCCTCCTCGTGTGTATATAAGTGTACCTTCAGTCTTATCTTGCCCACTATGGAATGGAGTATGTAGTTTTTTTATTACTGTGTCCGGCTAAGCAGTTTCTTCCATCTTCCAAGGCCGCCTTCCACCTTCGATACACGCCGCAGTAATAACAGTCCGGCATAAAAAGCATACCCTGCAGACAGTTTGCCTGTGCATACCGCTTCCGTAGAGAAACATGGTTCGTCCCGGAACACCGGGGCAACGAACATCCGCGGATTCCGCTGGAGTCTGACGAAACGTGACACCCAGCCGATCATCGTCCACTTCATGCCCCATAAGGCCCCCGCCGCAGTTGCCGTATCAGCCGCATCACCCAGCGAGAAATCCGTGGACCAGTCCAGCTTGGTAATCTTGACATGCGATAATGTGCCAACCAGCCATTTTTTGAGCCCACGGGTTGCCTTGAGTGCAGTACGGATGTTCTTTAACCATTCCGTCACGGATTCCCGGTCAATTTTTTCTTCCTTGTCACTGTCCATTTTCACCGGTGCGATTCCGCTTTTTTCGAGTTTAACTTTAATTCCTTGTTCGAGACTATCAAAAACCAGCGCAGGCAGCTCATAATGAAATTTGACCAGCCCGAATACAGCTTTAATATCAAACTCAATACGGTCATCCTTTCCCAGCCTGCACAGACGGAAATGAAAATGAATCGATGAAGCCAGAACCAGCACGAACAGCAGAATAACCAGCAGCAGCAGGCATAAGGGTATCGCAAGCCATAACGTCACAATCGTAACCTCCAAGAAGCCTCAGATAATGTGAATAGCGGAGCCTCTGATTTAGTATGGCAAATCCTGCTGGATAAAATTCGGCATTTCTGCAAACATCTCCAAAAAGAATCTGCAGCCAAAAAAAAATGCCGCTGTCCCGGCGGGGACAACGGCATTTATAGAACAGCGTTCATCCGCTGCGTTTATTCTGTCTCTACCTCTTCAAAGGTCATCTGGCTGTCCAGCTTGCTGAACAGCAGCTGCGTCTCTTCTTCCAGGCCCTCTGAAGTATCGAAGCTCGACGGCTCCGGAAGCTCCTTCAGGCTGGCCAGGCCAAAGCTGTCCAGGAAGGACTTGGTCGTTCCGTACAGGATCGGACGTCCGACAGCCTCCGCCCGGCCCACCTCATGAATCAGATCCTTATTCCCCAGCGTATGAATGGCCCGTTCAGACTTCACACCACGGATTTCTTCGATTTCCACTCTCGTGATAGGCTGGCGGTAAGCCACAATCGCAAGTGTCTCCAGCGCTGCCTGGGACAGGGATGATCTGGAAGGGGAATACGCCAGACGCTCGAAATACTGTGCATGCTCTGGAAGTGTCGCCAGACGGTAATTCCCGGCGATCTGCACTACCTGCAGGCCCCGGCCCTGCGAAATATAATCCTCTTTCAGATCCTCAAGCGCTCTTGTGGCCAGATCGGGCCGCTGCTCGGTAATTTCGGCAATCTGGCGGACGGATAACCCTTCATCCCCTGAGAGAAACAGCAGGCCTTCAATAATTGATTTCAGCGTGTTGTAGTCCACTGACTTCCTCTCCTCCTCTCCACTCCATCACAATATCGTCAAATAATTTCTCCTGGTAGCAGAAAATCGCCTTCATCTTCATCAGCTCCAGAATAGCTAAGAAGGTCACTACAATCTCATGCCGGGCCATCTCATCATGCAGAAGCGACGAGAAGCGCAATCTGCCGCCCATCCCTTTACGCTGCAGTGCTTCCGTCACATCACGGATCCGGTCCTTCACCGAAATCTCATCACGTGTAATCCGCTGATAAGAGGATCTCCGGGCAGCCTTGCTCAGCGCCTTACGGAACGCCGCAATCAGATCGGCGGTATGTAATCCCGTCAGCGGATTGTCAATCTGCGTAGGAACAAAGGGGCCCAGATCCTCCGGCTCCTTCGTGAAAATAAGGCTGCGCTCACTCTCCATATCCAGCAGCTGCACGGCAATGCTCTTGAATTTGCGGTATTCAATCAGCCGCTGTACCAGCTCCGCACGCGGATCATAACCGTCGTCCTCGTAATAATCGAAATCCTCAATCTCGATCACCGGCGGCTTCGGCAGCAGCAGCTTGCTCTTGATCGACAAGAGGGTAGCAGCCATGACCAGAAACTCGCTGGTGATATCCAGCTCAAGCTCCTGCATCCCCTGCAGGTATTCCATGTACTGCTCAGTGATCTCGCTGACCGGAATGTCCTGGATGTCGATTTCCGCTTTGTCAATCAGATGCAAGAGCAGATCGAGCGGACCTTCGAACGTCTCCAGCTTGTACAATACAGTCACGCGGTTTCCTCCAGCCCAAAAAAAGTAAAGTGCAGCGCCGCACGGACGCTACACAAGTAGAAAGATCTATGATCATGCTTTCTTCTCATACTTATAAATAAGCACGATTTGAACTGATTCGTCAAGAGGGGTGTTATTTAAAAAGCTTGTTAAGATTAGCCATTTCGATCGCAGCAGTTGCCGCATCCCAGCCCTTATTGCCCGCTTTGGTTCCGGAGCGCTCAATGGCCTGTTCGATATTCTCGGTCGTCACAACACCGAAGATCGTCGGAACGCCTGTCTTGAGATTAATTGCCGCAACTCCTTTGGCAACTTCATTGCACACATAATCATAGTGTGTTGTAGATCCGCGGATCACAGTACCCAGCGTGATCACCGCATCATACTTGCCGCTTTCGGCCATTTTTTGCGCGATTAGAGGAATTTCGAATACCCCCGGTACCCAGGCAACATCCACTTCATCGTCAGCTACACCATGGCGTTTGAATGCGTCGAGCGCTCCGGAGAGCAGCTTGCTTGTAATGAATTCGTTGAAACGTCCTACGACAACCCCATATTTCAAACCCTCGGATACTAAATGTCCTTCAAAATAATTCGGCATTGTGCTCATCAACCCTTCATGTATAATTTAGTGATTCTATGATTAAATTTTGGAATCCTCGTTCTGTTCGATCTTGTCAAAAGTCAGCAGATGGCCAAGCTTGGCCTGCTTCGTATGAAGATACTTGGTGTTGTCCTTGTTCTCCGGCATCTGGATCGCCACGCGCTCCACCACTTCAAGGCCGTAGCCTTCCAGCCCTTTGATCTTGCGCGGATTGTTGGTCAGCAGTCTGATCTGGCGGACGCCCAGATCCTTGAGAATCTGTGCACCGATGCCGTAATCACGCAGATCCGCCGCGAAGCCCAGCTTCAGGTTGGCATCTACCGTATCCAGTCCTTCTTCCTGCAGCTTGTAAGCACGCAGCTTGTTGATCAGGCCAATGCCCCGGCCTTCCTGGCGCATATAGAGCAGCACCCCTCTGCCTGCTTCTTCAATCTGGCGCAGCGCCGCTTCAAACTGCGGGCCGCAGTCGCAGCGGTGGGAATGGAATACATCGCCGGTCAGGCACTCGGAATGCACACGCACCAGCACCGGCTCATCACCAGAGATATCCCCTTTTACCAGAGCTACATGCTCTTTGTCATCCACTTCGTTTGTATAGGCAATCGTCTGGAAATCACCGAAATCGGTCGGCAGATTCACCGCTACCTCGCGGGTAACCAGATGCTCCTTCTCATTACGATAGTGAATGAGGTCCTTGATGCTAATCAGCTTGAGGTCATGCTTCTTGGCGATCTCGATCAGATCAGGCAGGCGGGCCATCGTGCCGTCAACCTTGACCACTTCACAAATAACGCTCGCCGGATAGGCACCGCACATGCGGGCCAGATCGACAGCGGCTTCCGTGTGGCCTGAACGCCGTAATACTCCGCCCTTCTTCGCGATCAGCGGGAACATGTGGCCCGGTCTGCGGAAGTCGGAAGGCTTCGCATTCGGATCCAGCATCGCCTTGATGGTCATGGATCTTTCCCCGGCGGAAATACCGGTAGTGGTATCCTTGTGGTCAATCGATACGGTAAAAGCGGTGCCGTGGTTATCGGTATTCTGGGCCACCATCGGCTGCAGATCCAGTTCCTCTGCACGTTCCGCGGTAATTGGGACGCAGACCAGGCCACGTCCTTCGGTGATCATGAAGTTGATAACTTCAGGGGTTGCCCGTTCGGCAAGCGCGATGAAGTCCCCTTCATTCTCGCGGTCCTCATCATCCACAACGATAATGACCTTCCCGCGCATCAAATCATAAATTGCATCCTCAATCGGGTCCAGGACGCTGTCCTTCTTGTCTTGCTGGCTCATGTTACTGTCCTCCTGATGGCTGTACGCTGCCTTGCCGGCTGCCGTATGCCTAATCTTTAATTATACAAACCCGTTAGCCGCCAGAAAATCGTGGCTGATCTTCGAGCTCTTCTTATCTTCTTCATCGCCGGAACGTGAACCATAATGCAGCAGATGATCCACATACTTGCCTAGCACATCACATTCGATATTGATACTGTCACCCGGCCGTTTGTGGGCCAGCACCGTTTCTCCAAGGGTATGGGGAATGATGGAGACAGTGAACGTGGACGACTCCGTATTCACTACGGTGAGACTGATGCCGTCAATCGTAATGGAGCCTTTGGGAATGATATACTTAAACAGCGATTTGCGGTCCGGCGCAATTTCGAACACGACCGCGTTCTGATCGCGCTTCACGCTGCGGATCTCGCCCGTTCCATCCACATGACCCTGGACAATATGTCCGCCGAAACGTCCGCCGGCTGCCATCGCGCGCTCCAGGTTCATTTTGCCCCCGGTCCGCAAGCTTTTGAGATTGCTGTTGCGGTACGTCTGAGGCATCACATCGACCGTGAAAGAATGATCGCCTATGGACGTGGCTGTAAGACAGACCCCATTGACGGAGACACTGTCGCCAATCTTCAGATCACCCATAATGAGGGAGGCGCCGATATTCAGCACCATCATCTCACCCCCGCTGGTGACGCTGCGGAGGATACCCACCTCTTCAATCAAGCCGGTGAACATTATATCCCTCCTTCAAAATTACAGTTTTCATAAATAAAACACTGTCCCTAAATACGCTTCTGTTAGCGCGCCGGGGTGCCGCTGATACAGACATTATCCCCGAGCACTTCCACTTCCAATCCTTCCAGCGTTACCGCATCCCGCATCAGCTCCACGCCCGGGAAGTCGAAGGTTCCTGCTGCTGCTGCGCCGCCCCCGACAATCTTCGGAGCGAAGAAGAGGACTACACGGTCAACCAGTCCCAACTCCAGCATGGCCCCGTTCAGCGTGCCGCCGCCTTCGAGCAGAATCGAACCGATCTCCATCCCGCCTAATGCAGCCATGGCAGCCTGCAGATCGACACGCGGTCCGCTGCCTGCGGCAACAACCTGAACACCTGCAGCGAGCAATGCTGCCTTGCGGGCCGGATCGGCCGCTTCTGTAGTAACGACTACTGTGGGAGCCAGCCCGTCCGTGACTACGGCGCTCTCCAGAGGCAGCCTCAGTGTAGAGTCGATGATAATCCGGATTGGATTCAACCCGGGCACATTTAGTCTGGTCGTCAGTGAAGGATTATCGGCAATCACCGTATTCACCCCGACCATTATTCCCTGATGGCGATGGCGCAGGGTATGTACAAGCTCCCGGGATTCCGCATTCGATATCCATTTGCTGTCCCCTGTACGGGTGGCGATTTTGCCGTCCAAGGTGCTTGCGCTCTTCAGCGTAACGAACGGCTGCTTCGTCAGAATGTATTTGATGAACTTCTCATTCAGCCTGAGTGCGCGGCTCCGAAGCAGGCCTACCTCCACCTCAATGCCCTGCTCACGCAGCATCTCAACACCGCGGCCTGCAACCTGCGGATTAGGATCTTCACAGGCAACGACAACCCTTGCCACCCCTTCATCGATCAGTCTCTGGCTGCAGGGAGGCGTGATACCATAATGGCTGCAGGGTTCGAGCGTCACGTATGCAGTGCTTCCCTGCGCCTTGCCTGCAGCCATGTTGAGCGCATGGACCTCGGCATGCCCGGTACCGCGCTGCAGATGGGTGCCAATCCCGATCATCGCGCCATCCTTCACAACGACACATCCGACCACAGGATTAATCCCGGTCTGACCTTGAGCCCTCTCCGCCATGTCCAGCGCAAGGGACATATAAAACTCATCATTCATCTTATCCAT

Protein sequences of DBSCAN-SWA_5

>NZ_CP009285|5329911:5337936|5331903_5332599_-|WP_042215614.1|DBSCAN-SWA
MTLWLAIPLCLLLLVILLFVLVLASSIHFHFRLCRLGKDDRIEFDIKAVFGLVKFHYELPALVFDSLEQGIKVKLEKSGIAPVKMDSDKEEKIDRESVTEWLKNIRTALKATRGLKKWLVGTLSHVKITKLDWSTDFSLGDAADTATAAGALWGMKWTMIGWVSRFVRLQRNPRMFVAPVFRDEPCFSTEAVCTGKLSAGYAFYAGLLLLRRVSKVEGGLGRWKKLLSRTQ
>NZ_CP009285|5329911:5337936|5332784_5333387_-|WP_042215617.1|DBSCAN-SWA
MDYNTLKSIIEGLLFLSGDEGLSVRQIAEITEQRPDLATRALEDLKEDYISQGRGLQVVQIAGNYRLATLPEHAQYFERLAYSPSRSSLSQAALETLAIVAYRQPITRVEIEEIRGVKSERAIHTLGNKDLIHEVGRAEAVGRPILYGTTKSFLDSFGLASLKELPEPSSFDTSEGLEEETQLLFSKLDSQMTFEEVETE
>NZ_CP009285|5329911:5337936|5333355_5334147_-|WP_042215619.1|DBSCAN-SWA
MTVLYKLETFEGPLDLLLHLIDKAEIDIQDIPVSEITEQYMEYLQGMQELELDITSEFLVMAATLLSIKSKLLLPKPPVIEIEDFDYYEDDGYDPRAELVQRLIEYRKFKSIAVQLLDMESERSLIFTKEPEDLGPFVPTQIDNPLTGLHTADLIAAFRKALSKAARRSSYQRITRDEISVKDRIRDVTEALQRKGMGGRLRFSSLLHDEMARHEIVVTFLAILELMKMKAIFCYQEKLFDDIVMEWRGGEEVSGLQHAEINY
>NZ_CP009285|5329911:5337936|5334280_5334748_-|WP_036727378.1|DBSCAN-SWA
MPNYFEGHLVSEGLKYGVVVGRFNEFITSKLLSGALDAFKRHGVADDEVDVAWVPGVFEIPLIAQKMAESGKYDAVITLGTVIRGSTTHYDYVCNEVAKGVAAINLKTGVPTIFGVVTTENIEQAIERSGTKAGNKGWDAATAAIEMANLNKLFK
>NZ_CP009285|5329911:5337936|5331332_5331821_-|WP_042215611.1|DBSCAN-SWA
MSDHPIQGLMQTAMENIKGMVDVNTIVGDPVETPDGSIILPISKVAFGFAAGGSDFRVEDDAPGVNGSGTGVKMLPFGGGSGGGVSIRPIAFLVVGRDGVHIVPLDNQTHLFEKIIDATPNLIDKIQNMFQPGGIPVGNDAHVAEVTKTVVKTEPTTHSSAH
>NZ_CP009285|5329911:5337936|5329911_5331156_-|WP_042215609.1|DBSCAN-SWA
MNMKTLTRKSLISLILCLLLLALVPLSSIRAENSSISTHARAAALIDVESGRLLYSSRGDEPMLIASLTKIMTALVAIENGNLTSKVKVGKNAFAKEGSSLYLKQGEEMTLEDMLYGLMLRSGNDAATAIAEHVGGSEQGFVYLMNAKAEALNLTHTHFANPHGLDAEGHYSSANDLAVLTAYAMHNPVFKEIVATKEKTADNPYEKWDYKWSNKNKMLRLYEGADGVKTGYTKKALRCLVSSATRNGQQLVAVTLNDGNDWNDHSALLDFGFNHYPLKTLVERGEAVSGYSLVTGKDFAYPLGQGEEARLITKLVLSEEKSAGVADARGNSGTGASSSANASSFGLKGVIIMQLGGKEIGRVPVYTPSQLPPETSAYEKKYSPAGGTAYPADNWLQAFGSALRALFQSGEDQR
>NZ_CP009285|5329911:5337936|5336835_5337936_-|WP_042215624.1|DBSCAN-SWA
MDKMNDEFYMSLALDMAERAQGQTGINPVVGCVVVKDGAMIGIGTHLQRGTGHAEVHALNMAAGKAQGSTAYVTLEPCSHYGITPPCSQRLIDEGVARVVVACEDPNPQVAGRGVEMLREQGIEVEVGLLRSRALRLNEKFIKYILTKQPFVTLKSASTLDGKIATRTGDSKWISNAESRELVHTLRHRHQGIMVGVNTVIADNPSLTTRLNVPGLNPIRIIIDSTLRLPLESAVVTDGLAPTVVVTTEAADPARKAALLAAGVQVVAAGSGPRVDLQAAMAALGGMEIGSILLEGGGTLNGAMLELGLVDRVVLFFAPKIVGGGAAAAGTFDFPGVELMRDAVTLEGLEVEVLGDNVCISGTPAR
>NZ_CP009285|5329911:5337936|5334790_5336044_-|WP_042215621.1|DBSCAN-SWA
MSQQDKKDSVLDPIEDAIYDLMRGKVIIVVDDEDRENEGDFIALAERATPEVINFMITEGRGLVCVPITAERAEELDLQPMVAQNTDNHGTAFTVSIDHKDTTTGISAGERSMTIKAMLDPNAKPSDFRRPGHMFPLIAKKGGVLRRSGHTEAAVDLARMCGAYPASVICEVVKVDGTMARLPDLIEIAKKHDLKLISIKDLIHYRNEKEHLVTREVAVNLPTDFGDFQTIAYTNEVDDKEHVALVKGDISGDEPVLVRVHSECLTGDVFHSHRCDCGPQFEAALRQIEEAGRGVLLYMRQEGRGIGLINKLRAYKLQEEGLDTVDANLKLGFAADLRDYGIGAQILKDLGVRQIRLLTNNPRKIKGLEGYGLEVVERVAIQMPENKDNTKYLHTKQAKLGHLLTFDKIEQNEDSKI
>NZ_CP009285|5329911:5337936|5336104_5336773_-|WP_042215623.1|DBSCAN-SWA
MFTGLIEEVGILRSVTSGGEMMVLNIGASLIMGDLKIGDSVSVNGVCLTATSIGDHSFTVDVMPQTYRNSNLKSLRTGGKMNLERAMAAGGRFGGHIVQGHVDGTGEIRSVKRDQNAVVFEIAPDRKSLFKYIIPKGSITIDGISLTVVNTESSTFTVSIIPHTLGETVLAHKRPGDSINIECDVLGKYVDHLLHYGSRSGDEEDKKSSKISHDFLAANGFV

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042215609.1|5329911_5331156_-	D-alanyl-D-alanine carboxypeptidase	A0A1P8VVG5	Erythrobacter_phage	2.2e-07	33.3
WP_042215611.1|5331332_5331821_-	GerW family sporulation protein	NA	NA	NA	NA
WP_042215614.1|5331903_5332599_-	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_042215617.1|5332784_5333387_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	2.4e-15	33.0
WP_042215619.1|5333355_5334147_-	segregation/condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	1.9e-07	36.2
WP_036727378.1|5334280_5334748_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	9.5e-44	58.3
WP_042215621.1|5334790_5336044_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	1.7e-116	53.7
WP_042215623.1|5336104_5336773_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	1.9e-37	38.9
WP_042215624.1|5336835_5337936_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	1.5e-52	36.9

Sequences of DBSCAN-SWA_6

Nucleotide sequences of DBSCAN-SWA_6

>NZ_CP009285|5399383:5440013|DBSCAN-SWA
AATGACTATTTTACCCGAAATGCAGCTGAATAATCTATTTGAAAATCTTGTCACTCAGTTTGTCAAAGACAACATGGAATCCATCATGCGTGCCGAAATGCAGGCGTTCATGGCGAGCGAGGAAGCCGGTACACGTAATAGCCGCAACGGCTACTACACCCGGAACTTGCACACGAAATACGGCAATCTGGAGGACCTGGAGGTCCCCCGCGACCGCCAGGGACTGTTCCAAACTCAGATGTTTGAGCCGTACCAGCGGCGGGATGGTTGGCTGGAGGAAGCGGTGATCCAGATGTACAAGTCGGGAATGGGAACCCGGGATGTGGCCCGTTTTATTGAAAGCATGTTCGGAAGCCATTACTCTCCAACCACCGTTAGCAACATTACCGCTACCGTCCTCGAGGATATCCACCAGTGGCAGAAACGACCGCTGAGCAAGCGCTACAGCGTGATCTATTTGGATGGGCTGTACGTGAAGCTCAAACGGGGTACGGTCCGAGGCGAGGTGGTTTATTTTGCGATGGGGATCGACGAAGAGGGACAACGTCAAATCCTCGGGTTCTACGTCGGCGGTCAAGAGAGTTCGAACGGCTGGCGCGAGGTCCTGAAAGACCTGTACAACCGTGGAGCGCAGGAAGTGTTGCTCGGTGTGTTTGACGGGCTTCCAGGACTGGATGCGGCGTTTAAAGAGACGTATCCGCAGGCAGATGTGCAGCATTGTGTGGTGCACAAAGTGCGAGCGACCTTCCCCAAAATCCGAATCGAACACAAAACCGATGTCCTGGAAGACCTGAAAACGGTGTATACCGCACCGGATGAGGTCGTGGCCCGGGCTCACTTTGATACGGTCAAAGCGAAATGGAACAAGCTGTATCCGAAGGAAATGAAGTCCTGGGAGGAACAGTTATCCACGCTACTGACGTTCTACAAGTACCCGGAGCCCATCCGCAAAGCGATCTACACGTCGAATCCCATTGAGCGCATGAACAAGGAAATCCGCAAGCGCCTCAAACCGATGAACAGTCTGACGAATATGGATGCGGCAGAGAAAATCGTGTATCTGGAGATGCTCGACTACAATGAACGTCATGCGCAGCGGGTCGTCCCAGGCTTTGGGATGGACAATGTCAAAAAGAAGCTAAACGAGCTATTTGAAGCACGCTATCCTTCCTTGCCTACACCCGAAGAAGAATAGCGGATGAATCCAGTTTCTGGGGGTCGGGGTTCCCCCTCCCCCCAGAAACACCTACACCCCAACCCGTAACCCGGGGAGGTACTTCTACTCTCTTACACAAACTTCTTGACGCTACCCGCCAAGCCGGTAAAACGGAAAATTAAATGTACTTTTTCCAACCAAAATCCAAATATCAGCGTTTCAAGGATAATTAAATGCCCTTTTTCCACTTATCTTACGGGGGCGGTCCTGAACAATCCAAAAAGCCGTACAATCAGCGAATTGCTGATGTACGGCTTTTTGGATTGTTTGAGCAACCGGAATCCGGTCTAGTACCGTGTAACCCCATCCTTAGTCACCAGCGCAAATACCAGCGGCTGCGGAGGAACCGGCTGCGCGGAGATGCGGTAAGCTTCCAGCACCTTGGCTTCGGCTTCCTGCACTTTGCTCTCGCTGGCGTCATTCACATGCAGTACGGCAAGCGTGTCGCCTGCGGCTACGGCATCACCGACCTTCAGCGACAGCTGAATGCCAACGGCCAGATCGATGACGGACTCCTTCGTTTCACGTCCGGCACCGAGCAGCATGGCGGCTACGCCGATCTCTTCAGCCTGAATGCTCTCCACATAACCTGCGGTCGCAGCTTTCACTTCGATGAACTTCCGGGCTGCCGGCAGGGTGTCAGGAGACTCGATCTGCGAGACATCTCCGCCTTGGGCAGTTACCATCTGCTTGAATTTATCCAGCGCGCTGCCATCCTCGATATGGGACAGCAGAATGGAACGAGCTTCTTCTTCATCCTTCGCCTTACCGCCAAGCACCAGCATCTGGCTGCCCAGAATCAGGCAGACCTCCTGGAGATCCTTCGGCCCGTGGCCCTTCAGGGTCTCAATGCCCTCTTTGATCTCCAGTGCATTGCCGATGCCGAAGCCAAGCGGCTGGTCCATGTCGCTGATTACAGCGACCGTGTTGCGGCCGAGATGCGTGCCGATATCCACCATTGCCTGTGCGAGCGCAATGGAATCATCCAGCGTCTTCATGAATGCGCCGCTGCCGGTCTTCACATCAAGGACGATAGCATTCGCACCTGCGGCGATCTTCTTGCTCATTACGGAGCTGGCAATCAGCGGAATGGATTCCACGGTGGCGGTCACATCACGCAGCGCATACAATTTCTTGTCCGCAGGCGTAATGTTGCCGGACTGGCCGATGACAGCCGCACCGATCTCCCCTACCTGGGTGAAAAAGCGCTCGCGGTCCATCTCCACGGAGAATCCCGTGATCGACTCCAGCTTGTCCAGGGTGCCGCCGGTGTGGCCGAGGCCGCGTCCGGACATTTTGGCTACCGGAACTCCGGCTGCAGCTACAAGCGGTGCAAGAACAACGGTTGTCTTGTCGCCCACGCCGCCAGTGGAATGCTTGTCAACCTTGATGCCGGCTATCGGACTGAGATCCACCTGGTCACCGGACATCGCCATTTCCAGGGTCAGATCGCCGGTTTCCCGTGCGTTCATTCCGCGGAAATACACAGCCATCGCCCAGGCGGAGATCTGGTAATCAGGGATTTCCCCCTTGCTGTAGCCTTGAATCAGGAAAGCTATTTCCTCACGGCTGAGCTCTCCGCCGTCTCTTTTTTTCTGGATAAGATCAACTGCACGCATTATACCTGAACCTCACGGACAAAGGAACGCACAAGGCCGATGAACTTCGGCTTAGTAAGGTTTGCTACCTTTACCACCTGCTCATGAGTCAACGGCTCCAGCTCATCCCCGATCGCCATATCGGTGATACAGGTAATGCCGAGCACACGCAGCTTGCTGTGGCTGGCTACAATAACTTCCGGCACGGTGGACATCCCAACGGCATCGCCGCCGAGGTAGGCCAGCATTTTGAGTTCAGCCGGGGTTTCATAGGTAGGTCCGCTGATGCCGGCATACACGCCTTCCTGCAGCACAAGGGCTTCACCGTCTACACCCTTAACTTCACCCGCCAGCTTCTTAGCCAGCGCAATATATTCAGGGTCATAAGCACGGGACATATCCGGGAAACGAACACCCAGCTCCGGATCATTCGGTCCGATCAGCGGGTTGTCGCCGGTCATGTTCAGGTGGTCGGTAATCAGCATGAGGTCACCGGCTTTGAACGCTCTGTTCATTCCGCCGCCTGCATTGGTAATCACGAGTGTGCCTACACCAAGCTTAGCCATTACGTATACCGGCAGCACCACTTTGCGCATTTCATATCCTTCATAGTAGTGGAAACGGCCCTGCATGATGATAACGTCCTTGCCTTCCAGCTTACCGATTACGAAACGTCCGGCATGACCCTCTACCGTCGAGCGCGGGAAATGCGGAATTTCTTCATAGGGCAGATATACGGCATCTTCGATCTGGTCGCCCAGATCCCCAAGGCCGGAGCCCAGAATAAGTCCGATGGCCGGAGTGTAAGAACCGAATTTGGATTGAATATATGCCGCAGCTTCTTTTACCTGCGTGCCGTATGGGACTGTTGATGGTGTTGTCATAGGTTGATCCTCCCGGATATGAATTGTCTTGTAAATAGCTTGAAGCAGGAACTACATCTTCGGAATAAAAGCCAGCACCAGCTTCAGGAATTGCTCGCGCACACGTTCCGCTGTCTCCATCACTTCTGCATGGTTGAGCGGCTGTTCCAGAATTCCGGCAGCCATGTTGGTGATGCAGGAAATACCCAGCACTTCGATACCGGCATGGCGGGCCACAATCGTCTCAGATACTGTGGACATCCCTACTGCATCTGCCCCTTGACGGCGCAGCATAACGATCTCAGCAGGAGTCTCGTAGTTTGGTCCGAGCAGGCCGGCGTATACGCCTTCCTTGAACTCGAAGTTCAGCGCTGCGGCAGCTTCTTTGGCGGCTGCAATCAGGCGCGGGCTGTAAGCTGAAGACATATCCGGGAAGCGTACACCCAGCGCATTATCGTTCGGTCCGGTCAGCGGGTTGCGGCCTGTGAGGTTCAGGTGGTCCGTAATCAGCATCAGGTCACCCGGTGTGAACTCAGTATTGACCCCGCCGGCAGCGTTGGTTACCAGCAGGCTGGTTACGCCCAGCTCTTTCATGACACGTACAGGGAACGCTGTAGTCTCCGGTCCATAGCCTTCGTACATGTGGAAGCGGCCCTTCATCATTACGACGCGGCGGCCTTCGATCATGCCGATCAGCAGCTCTCCTTCATGTCCTTCAACAGTGGATACGGGAAAATGAGGGATTTCATTATAAGGGATGACTACTTCATCCGTAATCAGGTCCGCCAGAACGCCGAGGCCGGAGCCGAGGATCAGCCCGATTTCGGGGGCGACAGTACATTTATCTTTGATATATACTGCTGCTTCTTGAATATTGCTTTGGGTAACTGCGGTCATGGTTGGTTCCTCCTTGAGGTGGGTAGGATGAACTTTAGTCATCGACGTAAAGCTGAGCCGTCACTACGGTGATATTTGGACTTCCGGCCGCTGTTGTCACCAGATTTCTTGATTTATCTGCTGTCCGCATTTGAAATCCGGTGACTGCTGATGCTTCCGAAGCGAGCTTTCCTGCGGAAAGCTTTCAGGCGGTCGCTATCGCTCCTACAGTTCCAAATTTCCCCTTCGATTCTTCTCGCTTTTAGTTATATCCTTCAGTTCATCTTGATTTATTATTTATATTAAATTAATTCAGACAAAAAGCTCGTCCCGTACTGCGGTGCCTTCGCTCCGAAGTTATCGGCGATGGTAGCTGCTACATCAGAGAACGTCAGGCGGATGCCCAGGCTGCCCGGATTCTTGAATTTCGGGCTGTAGATCAGGAGCGGCACATATTCACGGGTGTGATCCGTTCCGGCATGGATCGGGTCATTGCCGTGGTCAGCCGAGATGATCAGCAGATCATCTTCACTGAGGGTGGAGAGCAGCTCAGGCAGCGCCTGATCGAACACTTCCAGCGCGCGGCCGTAGCCTTCCGGATCACGGCGGTGGCCGTACAGGGAGTCGAAGTCTACGAGATTGGTGAACAGGAATCCGTTAAACGGCTTGCGCAGCTCATCAATCGTAATCTGGATGCCGTGCTCATTGCTCTTGGTCGGGTAAGAAGCTGTTACACCTTCACCAGTGAAGATATCATTGATTTTGCCGACAGCAATCACGTCTTTGCCGATATCCTCCAGAGCGTTCATAACGGTCGGCTCCGGCGGCTTCACCGCATAGTCATGACGGTTCGGCGTACGCACGAAATTCCCCGGTTCGCCGATATAAGGACGGGCGATAACACGGCCGACAGAGAATTCGGGAGCCATCGTCAGCTCACGGGCGATCCGGCAGGCGCTATAGAGTTCTTCCAGCGGAATGATATCTTCGTGCGCTGCCAGCTGGAATACGCTGTCTGCCGAAGTATACACAATCCATGCGCCGGTCTTCATCTGCTCTTCGCCATATTCTACGAGAATCTCGGTGCCGGAAGCCGGCTTGTTGCCGATCACCTTGCGTCCGGTAGCCGCTTCGAATTTCTCAATCAGCTCTGCCGGGAACCCGTCAAAATAAGTATTAAAAGGGACCTCAATCTTCAGGCCCATCAGCTCCCAGTGGCCGGTCATCGTATCCTTGCCTACAGAAACCTCCTGCATTTTGCCGTAATAGCCTGTCGGGTCAGCTACCGGTTCCAGCGGCGGCAATGGAGCAATATTAGCCAGTCCCAGCTGTTGCAGGTTCGGAAGCTTCAGTCCCGGAACCCGTTCCAGAATATGTCCCAGCGTATGGGAGCCTGTATCTCCAAAATTAGCGGCATCCGGCGCTTCACCGATACCTACACTATCCAGAACAATAAATCCGATGCGTTTAAATGAGGACATTGCCGTCTTCACTCCTTCGTAGTTTACATAGTTGTAAGGTCTGCTCAAAACAGGAAGAAACTCCGGGAGAACCTCTCCCGGGAGCTATCCATTCAGTATGATTCCATCATAACTTTCTTACTCACAAAAAGCATCTTTTCGGCCAATCCAAACCATTACCCGTTCTATCCACGGTTACACCCAGCCTTAGATGACAGACTACTTCGCCCGTGGATGGTGATTCTCATAAACTTCCTTCATGTTCTTGCGTGCAATTCCGCTGTAAATCTGCGTGGTTGAAATATCGGAATGGCCCAGCATCTGCTGCACGGAACGCAGGTCTGCCCCGCCTTCCAGCAGATGAGCGGCGAAGGAATGCCGCAGGGTATGCGGTGTGATGTCCTGTTGAATACGGGCTTCACGCGCATGTTTCTTGATAATCTTCCAAAAGCCCTGACGGGTCAGCCTCCCGCCCAGACTGTTCAGGAACAGTGCCGGCTCCTCCTGGTTTACCCGGAGCAGCTTGTCCCGCATACCGGACACATAACGGGCCACACAGTCCGCAGCAATCGTACCAATCGGCACCACTCTTTCCTTGCCGGAGGCCCCGCTGCAGCGGGCGAACTTCAGCCCGGTATTCACGTCCTCCACATTCAGCGAGATCAGCTCCGTTACACGGATACCCGTAGCATAGAGCAGCTCAAGCATCGCCTTATCGCGCATCCCCTGGGGTGCAGATTCATCAGGGACGGCCAGCAGGCGTTCAATTTCTTCAATGCTAAGAATCATCGGCGGTTTCTTGCTCGGTTTAATCGTTTCCATATCGAGTGTCGGGTCTTGCCCGATCAGCCGTTCTTTCAGCAAAAAATGAAAATAGGCGCGCAGCGATACCGTATTCCGGTTGACTGTTGCCGTTGCCTTGCCCGCTCCGCGCAGAGCGCCGAGGTAGAGCATAATATGTGATCTTCTAATCTCTTCCATCGCAGCCGTGCCGCGTTCTTCGGTAAACTCCAGAAACTGTGATATATCCCGTCCATAGGATTCCAGCGTACTAGGAGACAATCCTTTGTCCCCGGACAAATACTGCATAAACGGCTGCAAGTGTGACTCCATCTATTCACGCTCCTGTCATACTCAGGCTGCTTCATGCGGCTCTGCAGCGGGTGGGGTCCGGCAGCAGTCAGAACGCTAACGTCCCTTAACATGCTCTAGATTTATTCGACAGGCTTCTAGCTTTTTCCTGCAAACGGCAGAGCGGTCACTCCCCGTACCAATAGTATAAGCGCAGGCGCTGCCCTGCACTAAGCCCTTCATCGCCCTGCTTCACATCGTGAAATGCCCGGATGGCTGTGCCCTCAGGAATATCATAATTCTGCGCTGGACTCATCCAGGCGCTGAACCAGCTTAAGATATAATACAGCACACAGCTTATCGCAACGAGCAAGGTCATAAAATACAGCCGGCGCACGGTTTTGGGAATCGAGACAATCATCTTAGGCAACCTCCTAAAAGTAATGTAAGCTTCCGCTACAATGTTCCACTTCGCAGAACTCGTCCTTCAATTTATGCGCCGGAGGGTGAGGTTATGTATTTAAATCAGTTAAAAAGCCCCCTCCAGCCATTCAGCCGGGGAGAGCTTGTGCGGTAAATCCTCATCTATAAGCTTATTCGGGAGTATTGCCTTCTGCAGGATTCTTATCCTTGCAGCGGTAGCAAATTCCGTGAAAATCAAGTCTATGATCAAGCACCGTAAAATTATAATCCTTCTCCAGCCGCTCTTCCAGCGGGCCCAGCCAATCCTCACGAATCTCATCCATGGTTCCGCATTGTACACAAATCAGATGATGGTGATGATGTTTCGCTGTATCCGTCCGCAGATCATAACGGGCCACACCATCTCCGAAATTAATCTTCTCCACGACATGAAGTTCGCTGAGCAGTTCCAGGGTACGATATACGGTGGCGAGACCGATCTCCGGAGCCTTTTCTTTCACCAGCATGAACACATCTTCAGCGCTTAAATGATCATCCTCGTTCTCCAGGAGAACTCTTAAGGTCGCTTCCCGTTGAGGTGTAAGCTTGTATCCTTGGGATTGTAGTTGTTGCTTAATCTTGTCTATCCGGGCTTCCATTGTCTGCCTCCCCCTTGGAAAATTACCGCACCGGGCTTCAAGCCACTTCTTCCATTATAGGGGGAGTTACTTTGAGAAGTCAAACGGTTTTAGGATGTATGCAGACTTAAATAGGCTTAATTGGTATGACATTAATACCTATGTGAATCCCCTCTTTAAAAAGTAGCCCCTTAAGGCGGATTCGTAATATATCCAAAAATTATTGGGATCAAATCCGAAAAACAATAACAATCGTAAACATGCCTTTCCATCAAAACGCCTTTTTTAATAGAAAGGACGATCTATGAGAAATACGTGTGAGGATCTGCATATGCTATTGAATAAACAGAAAGGAGGTGCTTTATGACTCTTTTACTAGATTCTCGCACATCACAAAATGCAAGCTTTGCCTCTTCTCTTGGCGTTCCTTTCCCAGCTATACTATCCCCCCAATTATACGGACAAGTCGGATTGAACATTGTGAGACCCACAGGGAATATCAGGGTAGAATTTTTCACTACCGTATCTATCTTACTACCTGCCGGCACTCCTCCAACTGGAATCTTCGTGATCATCGTTAGAGGAACCACTACGAACGATCCTATCATCTATTCCGCACTCGAAGTGTCTCTGCCATCCAATACGAATGAACAAGTGCTGCCCATCACGGTTATAGGTTCTGACTTCAATGTCCCTGCTCCTGAGAATAATCAATTGATCTATTCAGCATTTGTTAGCACAACGACCCTCGGACCGGTCCGGATCGGACCCGAAAGCTTTACCGTTACAGCTTACTCTGATTAATAAGAGTATACGAATAAAACCAGCAGTATGGGATATCCTGTACTGCTGGTTTTATTGTTTCTTTTATTGCAGTGGGAGACCTTGTTTTGAAGGTTTTTTGTTGCATCCATTTGATCATTTTGAAAAACACTACTATATTCAATCAATACTTACCAGCATCGGCGTCACCCACCGCATCATTTAGTCTAATTAATACAGTGAAATGGGGTGAAATACAGGGGTGATTATTTTGCTCATGGATATGATTTGGGTCATAAGAGAAATCCAGTAAAACACATTAAAAGAGAAACGGTGATTTTCGTGTGATTTTTTTATTTGTTATGATTACAGTTCCCGATATCTTTCTTACTATAATAAGGCTACACTTTTGGCACCCTCCCCGTCAATCTCAATACCTCCAGCTTCCGCTGCAGTTCCAGCTGCCATTCGTGGTCGTGTGTCGCTCCAGCCAGCACGGACTGATTTTGAATCATCAGACAGTCCCAGCAATACCTGGCATTCTCTCGCAGGCAATATTGCAGCTCCTTAGCCTCTTCGATCGTCAAAGGTCCAGTCATGTTAATGTGAAAGATCTCTGCCAAGCGTAAATGTACCGGTAACATCATAAATCACTCTCCTGTATTATCATCCTAATACATCATATGCAAGTGTATCAGAAAGATGATACGCGTATGAGGATATTGATACATTTATTTATGTGATGTATACTTTTGGAAAAAGGAGGCTTGTCCGTGATTAAGAATAACGTCAAGGACATCATGGACCGGCAGAATAAGGGGATTCGAGGCACTGCGAGGGAGACGGGGTTAGCAATCAACACGGTATCGGGGCTATATCATAATACGTCCAAGCGCGTGGATTTTGAGACGCTGGAGAAACTCTGCAAGCACCTGAAGGTTAGCACTGGAGAACTCATTGAATACATAGAAGACAAGGAAGCCCAACCGGAGTAATCCTGCTGGGCTTTTTCATATTTACCGAATTAATAAATAGAAAAATATCCCTACTTCTGATAGACTTATTTTGTAAATTGTTATCATAAATAGGGGGAAATTTGTTGAATAAGCCAATTTATACAAAGTGGTGGTTCTGGGTCCTGGCGGTCATCATTATAGGAGCTATCGGAAATATGGGTGATGACAAGAATACAACGGATCAAGCAGTGACCTCAGCCACTATAGAGCCGGCAAAAGTTGTTGTGGCAGAGGCCACAGAAGAGGCCGTAATTGTGCCGACTCAGAAACCTAAAGAAGTATCCAAATCAGATCCTACGGTCGCTCCCACTGAAAATCCGATACCGGGAACTATCGGCATGACACCTGAAGAGTTTAGGAAGGAATTCAATGCTCGTGCTGACTCTATGGAATCCAAGCTAAAAATCAGCAAAAAGCTCACTGTTGAAGATGGACTTGCCCAAGACACATTTCAGTACATGTTCAATGATTTCCTTGGCATAACAGGTAGTGTTAATAAGGCTGATGGGTCAATTAGAGATATAATGATGATAGGACGTGGAGACGGTACCTCTGCTTCAGGTGCAAACATCATTGTAGTCATGGGATTAGTAATATTAGCTGTCAATCCTGATATTGAGTCGACAGAGGTCGGAAGTATAATCACCGACTTAAAGGTACTTGAAGATGGTGTTGACCTTGCTAAAATTGATGAGTCCACTGTCAGAAATGGCATACGGTATCATGTACAGGGGTCAAATGAATTAGGTCTTATGTTCAGCGCTGGTGATGCAAACGATAAATAGTAAAAAGCCCTGGGGATGTCCCAGGGCTTTATTTATGTAATGACCCGGATCACATCATCGATCTTGATCCAGCTAAAGTCCTCTTCCATTTGGAACTTGATTCTCCTCAGCTGCCGGTCTACTTTCACCACAACGCCCCGCACCTTCAAATCCTTGTAAGGGTCAAACAGTACGATTGTGATCTGTTCCTTCTCCAGCAATGCATACCCGAGCGCCTGGTCAATCAGCTCCCATTCATCAGGGTCGATCGCGGGCCGGCTGCGTCTTCCCTGCTCCTGCATTTCCTGCCTCAGAAGCTGCACATGCTCTGGCAGCAAAAACCGACTACCTTCCCAAACACTCTCCAGTTTCTTTCCCATGATGTATCCCCCTAGTACTCGGTCCAGTAATCTATATTTCCCGTTATTTCTGCCTGCTGTGACTTGTGTGGGCCTGCCGCAACATGATCTTTAAAAGGGACGTCCCTTTCCCATGCCTCGATCACAACGGCCGTCTCAACCGGCTGCTTGTCGTCCCACTGAATGTAATACTGCTCGACCAGCTGCAGCATGCCTGCTTTGATCGCTGCAGATCTCCGACCGCTCAGCCGTTCCAACTCTGGCAGAGAGGGCATTCTCCGAAAGTGACCATGGAACTGAAACATGACCCGAAGCAGCTTGCGCGCCGTATCATCCAGCATGACGATTCTCCGCTAATGGTCTCCAGGATAGTACGTTTGCCACTAAGAACACGCGCGGGGCATTGGTGGTCAGGCAGGTGGCCCTAATACGGCCGTCACGGATGCCGAGGATTTCAATCTTCCGCTGCGTGATCTTTCCGGCTTTGTCCAGGTATATCATTTCAATGGTTTGGCCGATGCTCATTTTCATGTGATCGCCTCCGAAATAGGAACGTTTGTTTGTATTATATGCTCCCTACCCGATTTTTAGCAATGGTTTGATTTCCCACAAAACGCAAAAAAGCCCGCCGACCAGTTAAGGTTGACGGGCTTTTTGCCGATGCTTTCGGACTGCACGCTCGGTGCTTCCGATCCGTGTAACAATACAATAACACATTTGGAACATCTTGTATGAAAAATATTCCTAAACGCAACAAATACCCTCCATAACTGGTAGAGTAATGTTCTTTCCACTACAGCAATAACCACGATCGAATTCTTATGAAGTGATTTTTTTGGCAAAAGGTGATCTATCATAGAAAAAAACCCGCTTAGGGGTTTGAAAATCTGACTAGGATCGAATAAGTTTGTTATTGGCCTCGAAAGAGAACCTACGCTTAATTTGATCATTAATCGTTCTCGTTGTATCAGCAAAACCTAAATGTTCTTTAATAAACGTGAAATCATAGACTTCCAGCAGTTCGATGAATGCTGAATTAATAAAGGATGAAGAAACACTATCCATACCTTTAAAGGAAACAATAACTGAGTCTCCAGTGTCAAAATGTTTTCTTAGTACATCCTGTACAGCTTCACCTTCTGCATTGGAGTAGCAATGATTGACATGGTCACCAAGCCTTAATAAACGTCCCATGAAAACTCCTCCTCTACATATTCAATTGTGTCAGTCTGAAAAACAATTTCCAATAATGTTCCTGGATAAAATCCTTCTGTTTTTCTTGAAGTAATTTCCATCCCATCACGACCTGACGTTGATGATAGTATACCATGATTTGAATGGATGTAAACACTCCCCTTATTATTTATAACCACATTTTGTAAGAGGAAATCCAATCCCGCACCCCTATTTTTAGGTGTAGACTTTGTGGTAAAGCCTTCTTTAATCGCTAAAAGCAGGGCCTCCGCATCGTCAACTCCAGGAAGTATGTCTTGAATTGATGATGGAATTCCAACCCCAAAATCAGAAATAGCTACCATCACTCTGCTTTCTCTTGGATAATGTTGAACAAATATACTACCAGTATGCTCCGCAGAATGATCAATTATATTGTTAAATACCTCCACAAGACACGACTTAATATCTCCTAAGGATTCCTTTGTTAGATTCAGTTTACCTGCCAACCAAGACATAGCGTAATCCAAATACTCATAACTTCTGTTATACTCTACGTGTTCAAGTGGCAAAGTAGTCATCCGAAGAGAAGATTTCTCATCTAGGGTTCGATCTATGAATTTCTTAAAAAACATCGCATCATCCAGAAACGCCATGGGGCAGCGCCTATTGCTACGGTCTGGTTCGAAATATGTAATGGATAAATGTGCCCCTTGTTTCTTTAATCGCCCAATAATATTGCTCAAAACAGTTACACCTACCGGCCTAATGAATCTTAGTGGGGTGAAGTCAAAAACATAATCCCTTGCTCTAAGATCCATATTTTCATCAAAAACCTCATTAATAAAATAATACATATTATCTTTATCGAATTCCTTAGGCAGATATACTCTCAATGCATCCACAATCTCACCTCAAAATTATAATAGGTATATATTACCACTCAATGAAGGAATGGAATAGACCTAATTGTGGAATCCTTTTTAGAATTAAAAATGAGAATAATAATAAAATAAGCCCACCAGCCGAAGCCAGTGGGCAATTATTACTGTTTGGTCAATACTGTCGCTTTATAAGCGAGATATGCCTTCTCGATGGCCGCCCGGATCTCCTCTGGTGCAGCCTTGATGCCGCGCGCCTCCAATTGGTCCGAGGCATACACCAATGCCTGCTGCAGCTTATCCTCCCCGCCCAGCTCCTTGTAGACCGTCTGAGCGTAGGCAAAACCCTCGGAAGCAATCTTGTGCAGCAGTTCCCGCTGAGACACTGACAGCCGAGCATCGAAAAATGAGTCTGCCTTTACCTGCAGCAGTGCTATCGTCCGCAGTATTACCGTGGCCAGAATGCCGACAATGGCCAGCACAACGGCCGTGATGTACGGCTGAGCCTGATCAATTACAGTTTGCATATAAACCTCTCCTATTCAGTCGGCATGCACGCAGCGCGCCGCAGGTGATTTGCCGTATTGTTGTAGAAAGCCATAGCCGTCTTATCACTCTTAACCTTCGCCGCCTGCCAGCCGGGAGAAAGCCACCTGAACACCAACTCCTGGACATTGCTCTTCGGCAGTTGGGTGAACGGTGCTGCTGATCCCGGCTGCAACGGTATGCGGGCGGCCAGGCGAAGGTTATTCGCCAGATTGTGCAGATGCAGGGTGCCTACGGAGTCACCAGCCTTCCGGGCTGCAAACCATGCTGGGGATACGTAATCCTCAATGAGTGCCTGCGCCACGCTTGCCGGAAGCTGCAAGGCAGTAGGTGCCACGATTACCGCCGGCTCCTCCTGCATATCCTTGACAATGTCATACAGCAGGTCCTTCAGTGTCTTCCCGATAGTAGCCAGCGCCTGGTCAACATCACTCTTACGCGTCGGATCCAGCTGCTTATGGCTCGGGATGTGTGTCAGCGGGTTAAGCTTCCACTTGTCGCAGCAGAAGGCCAGATACCACACGTAGCGCTTGTACGCCTCCAGGGTATTAATCTTACCGCCGTAGCACAGCTCCACGCCTAAAGCGATGTCGTTGGCGTCATCGCCGTATTTGGCGTTGTCAGTGGTCACGTTGTACAGCACATGCCAAGCCTTCTCCGCCGGGTCCGTCCCGGTGCCGGTCGGGATGATCTCTAGGATGCGCTTGTCGTCCACGAAAACCTGCGCGGAGGCCGACCGGTTAACAAGGGTCTGAAAATACTCGAAGTGCTTATCCGCTGTAGCCCCGGGGTTTCCCGTATCGTGGGCAACTAAAAAGCCCGGCGTACCCGTTACTAACCGGGTGCCGGGCCGAACATTGGAACGCTTGTTGATATAGCGCCGCTCGATTGGGTATTTATTTTTGATCATCGTCTTCCGGATCCTCCCTTCCTTTTACCACTGGGCCGTTCTAAGAACAGCCCCAAATCTCTGCCCTGCACCAGAATGGCCAGCGCGCAGAGCGTAACCGTCGTGCCGATTACACCGATGGTCCAGCCCCATTTCTGCAGCAAGTCGAAATAGTAACCTGTCCATCCTTGAACCTTTCCGAACCGGATCACAAAGCCGACCAGGCGCTCCAATGCGTAGGCCGTGAACATCAACATACCAAGAACCAGCCCGATACCGACAACGCCCTCCCGGTATTTCTTGCGGAAATAGATGTGCATAGCTGCCGTGATATAAATGATGCAGATCAGCGATAACGCATAGCAGATGAGTGTAATGGTGTCGTTAGCGCGCATAGTTCTCCCCCTCTTTCGTACTGTGATCGTAAATAAAAGCGCCGGCGAATCCATTTGACCTGACAACTTCCTTATGTCGTTCATCCAGATCCTCATATCTCCGGATCGCCCACTTCACTTCCTGTTCTTTCTCTTCTAATTCCGCCTCTTTCTTTTTGATGGCGGGTATCTTTCTGAGCAGTTCAAACAAACTTACTCGCGGCATGTTACCCACCTCCGTCCTGGTCGCCCGGATTCAAACGATCTGCAGGCTTCATTTTCTCCATAACATCACTACTCCGATTTAGAGCAGCCACGGCGGATATGGCCTTCTCGATTGCATCATCCCGCTGCTTCTCCGCCTTTTCCAGCGACTTCCCCGGCACCAACTTACCAATAACCAACCACCTACCTACAATGACCAACAGCAACGCTTCCCCGAGCGCAAACAACCAGCCAATACCATATTGGTCCGCCAACGACAGGGCGTCTTTTAAGCTAGGCAAATCCATCCTCCCGCCCCTCTCTCTACATGGAAATAGCCCGCGGATCGGCTCCGAGGGCAAAAAAATAGCACGCTCCTCTTCAGGGCGTGCCGCTAATCAACCGGTGATTCCAAATCTTCTGCCACTTTGCTGTCTGCTGCCTTCATGCGGGCTTCGTCCAGTGCCGCCAGTGCTTCACCGATCTGCATGTCGATCTGCTGAAGCAACTCATACTGCCGGCCGGGATGGGAGTTGATGAGCAGCAGCACAACTGCCACCGCTTCCTGCACGGGATTGCTCGGATTCACCGAGAGTTCTAGATTGATTACTTTGGCCAGAGGGATCACCTCCTCTCGAGGGAATAAAAAAGAGCCCTCATAAGAGGACTCATTCTGAATTATCATCTACCCATCCGTAACTGGGGACATAATGTTGCGTGTTGCCTGTAATTACATTTACTTTTATAGGGTACGTTTGACCATTCTGCTCATAATTCAGATAACGATAAGGCGTCGGGTAAATCAATATGCTGAAAGTAAACAACAGCAATAAAACACCGGCAACCCAGACTATAGGTTTGTTCATGGCGTTGAGGGTTCATCAAGTAGCGTCTTAAGCCTGACAAGTTCTTCTTCATTAAAAGTTATGATCTTTTGCTTTGCTTTGATCATTTCATCAATTTTTGCCAAAGCATCAAGCTTCTGCTGTTCGGTCGGGTAATCAGCCGGATACATTTTGACTTTTTCTTTGGAGTCTTCCAAACCTTTAATTGCTCCTTGAGCGCTCTCAATTTCACTCTCAGCAGCCCGGATTTTATATTCAATAAATTCTCTTGAATCGGATTTGTCTGTGGATGTTCCGTTTGAGATAGTGGAATCCGAAGCTATCGTTTGAATGTCACTCATGATAATCTTTTTCCCCTCCACAGTCAGATTTGTCCCTACTGCTTCAGCAACTTCACGAACTGGAGCATAAGCCGAACCATTAATGATAACAGCATCACCAATCTTCGTTCCATCTGCTTTCTGTACCGTGAACAGCCCTTGCACTTTTGCACCGATTAATGGAGAACTTGCGGCAGCAAATCCAATCGACCCACCAAGCATAAGCGCAGAAGTCATAATGACAAAAACCTTCTTTTTCAATATTTCAACCTCCTGAATATAGTAATAACCCAAGTATATCCAAGAGGCTTATAAGATGGTAGGTTTTTTAAGAAACTGTGAATGAGCCTCCCCAGTTCACTGCACCAGCAATACCATGATTATGGGTTCCAAGGTTAACCGTGTGCGAATGACTAGCGCTTGCTTTCCCCGCTAAGGCGGACCAAATAGAATCAAGCTCAGCACGTAATCCGCTAACGAAATTAATACCGAAACCGGAAACACTATAGGCAGAAGCGAAATTCATTTGCCCTTGAAAAAATATAGTGTTTGTCATAGCAGATAAGAACAGATCGTTATCTCCAGCAGATCGCACTTCAAAAAGACCATCACCACCATTAATTACGCCACTACGAGTACCATTTGATTGATCAAATGTAAGTGCACTCATATTATATCCAGCATCCTGATAGATTCCGATGCGCCTGGTACCACTTGCATCATAAGTCCTCCATCCGGTTTCATCAACCTCGAACCTTGCTCCTGCAGCAGCAGTCCTGATCAGCGCCCCCGTCACTGTGCCAGCAATAATATCCGAATAGGTCATAGTACTCTCTTCAATCAGTCCTGTCAGCGTAATAGATCTCGCCACAACATTCCCGGCCATGTCCACCCGGAACGGCGCGCTGTTAAAGTCCGCATGCCCCGCGCTGATGCCGCTAGGGTTGATCTTGGTTATGTTATTCCCGCTACCAATCTCCATGCTGACGAAGCTCCCAAGCACCCCGGCAATGACTTCAGCAGCAATGCCCCGGCCGGTGATGGCCGTTCGCGCCGTGGCCCCGCCGTCCTCCGTGATAATCAGCCCATGCGATGTCAGAACCATCTGCACATTCGGATGATCCACTTCCTGCAGCACAATGCCGCGGCTGTCGTAAATGATCTCGCTCTTCGAAGCATTGATGTCGATGACGGCCTGCTTGGCAAATTCTTCAAACGCAGCTGCCCGTACCCGGCCACCGGACAGGAGATCATTAAGAATTTGTTTGCTGCGCTCCAGGTCCGCCAGCACCTGCGTATCATCCCGCATCTGGTAGTTGGATAGCGTCGCCTGAGAGTGCTTATCCATGCTGAACGGATACTCCGTCAGCTCCATCACCCGGCAGCTGACACGCTGTAGCTCCATTTCCGGATCATAGGCGTATACCGTATCGCCCAGGCCCGGCCGCTGCTCGTCTGGATCAATCTTATAGATGTCCGCCGCGCTGACACCGATCTCGAATTCTGGCATTTCCTTCTTCCGCAAAGCCTCCCGGGTAGCGATCAGCAACTCTTCCGGATCCTCGATGTTCTGATCGATGAGCTCACCGTCATAAAATGCGTTGACGTTGTTGGTCCAGTACTGAGTATACGGCGAGATCAGATAATTCACGGCCAGTTTATTATCAACGATGGCGCCCGGAACGGACTGCAGCAGGCTGCGTTCTTCCGTGGTCAGGTAGTCGGCGGAGAGGCCGATGAATGTCCGGCCGTCCTTCATCTGGGAAAACAACCGGGTTGTCAGGTTCGATACATTGTCCTTAAAACTATCGTTGATGATATTCTTCCGGATCCGATATTCGAATCCATCGTCACTGCCGATCCGCTTGTACAAATGAATGACGAAGTTATCCGGATCAATCTCGCAACCGTACAGGTTGACGGTATCCTGCAGGGCGGCCAGGGCCGTGGTCGCTCCCCAGTCCTTGACGTCCCGGAGATCAAATGTATCATGCGTGACAAAGGTGTAGATGCCTCCGGTGGCCGTACTGATCTTGTCCAGCAGCACGCTGATGTGAACTCCGTATGCCTCATCGATGTAATCGTCATATGGCATCTTGGAGTCGATCATTTTGAACATGATGTGCGTACAGATGATCTGGGCGCTGATCACTTTGTTGCTGCGATCCCGGGCACGGGACTGCACGACATAAAATTGGCCACGCTCATCTTGAACGTGGCCTTTGGGTATGATCAACTCTTTATAGTCGGTGCTCGTCATCGGGACGGTGAAGGATATCTCGTAGTCGCTGTTTAGCCGACGGCGGCGCTGGACGTCGGTGGTTGCAACCAGCAGGCCGGTTGGGGTGCGGTTGCGGTCGAAGGATTTTAGGTGCTTCTGCAAGGTGGACTCTCCTTTCAACGTAGCTCTGAACCTCTTTATGATATTAATTTCTAAACAATAATTTACCGATATAATGTATAAACGCACTATAGGGAGTGATTAATATGAAAGAAATCTCTAAGGCTAAACGGGCAATTGAAGAAATTAAGAATCTTGAGAAATATTATAAAAGTCAATTGACTATAGAAGAAATCTCTTATTTAAAATTCCATTTCGATAAAGAAACAGAAGTGCTAAAACAACCGTTCATAAATGTTGCCGCAATATCTTTCGGTGCATTTGTAGTTGGTTTAATGATTACGCAAGCGTTTAAGGAAAATTTCCTTTCAGCTGTATTTATATTAAGTGTTATTTTTCTAGTATATCTAGGGATTATGGGTTCGATGCATTACAGTAAACTAAAATACTACACGATAAGAAAACACATTACCGAAAAAATCCTTAATGAAGTCGAACAAAAAGAGCCGCTGGAGTGATCCGGCAGGCTCTTTCTAATCACAAATCAATACTATTCGCTGGTTTTGTCAAGGTCCGAAAGCATGCGCTCTAATGTCTCACGATCATAAGCTGGTTTTATAATCTTCCAAAGTCTCTTAGCTTCTTTCAGACTATAGAGATGCCACTTCGGTTTGATATTCATCGGTTCATATTCATCGTACTCTTCAATAACCTCGAAACAATCTAAGCAGACCCAGTAAAATTCCCCATTACCTTGAGGTATTTCCCTGAATTCAATTGGTTCACCATTACTTAGACTTTCAGTGTGGTCTTTACCGCAAAATTCGCACTTCATTCGCTTCACTCCTCGAAAGTTTTGTAACTCGTAAGCAAGATATTTCTCTTCTTGCTACTCGAGAATAACACTTTCAATCCCCTATATTAATGGGAAATGAGGTGAGACGAGAGATTCGCGTGAAAGTGATGGAGATTAGGTTCCGTTGGATCGAGATTAAAAAGTGGATTCAGGACATTAACAAAATACCACTGAGTTGAACCACTTAATACTGGTGTTGAAATGTTGAGTTGAGAAAAATAATTTCCAATTTTTTGTCTAAATAATGAATCTTATATCTTTTTAAAGCTCTTTGAGGTTTTTAATCCTCATTTTCTGATATCATGCTACGCAGTTTGATCCTTTATTTCATATAGAAAACAAAAAGTTCCCTTTGCGGCTTTCAGTGTCAACTTGTTGCTCACGGTTTGGACCCGTACCGCAACATCGTATCCCCTTGGCGACCGCATTAGGAACTCCATTAGTATACAATTCCGCACACGTATTGTAAATATCCCACTAAAACCCAAACTTCCCCGTGATGATTAATAATCTTCGCTCTTCTTGACAAGTATTTCGTTATTAAAGGAACTTGACTAATCCAACTGAAGCTTTAATAGATGGAATTCCTAATTCTTTAGCAAGTACCGCTCTGTGATTTCCCATTCCTCCTACTAATAGATCACCATTTGGAAGCTCAATTAAGTAAATGCCATCAGGTCTTTCATTCGTCCACCCATTCTTTTCAACGCTCTCCTTAAGAATGCCCATCTTGTAATCATTGAGTATTGAAGGATAGTCATAAGATTCATTAATTGCGATTATTTTCTGTGGATCAACATCTTTTAGTACCGCACCAAGCGTTGTTGCTGCCTTATCTTTGTATTTCTCCTGAAACTTTTTTATTACTTTCTCTGTTGTCTTCCACTTCTTCGCCATTTATATTCTCCATTCTATTTCCATTTTCATACATTCTACTATCAGAACGGAGAAAGTGTAAATAGCAATGCTAAAATTCACCACGCGATTACCGTCTACCTGCTTCATAGCCTATTTACACTCGATCCCGTTGCTGTAAATCCGGTCGCTGACTTACTCGTAGAATATAATTCGTTTCCGGTAACGGTCAAAACGTCAAACGGCAGTCCGAACTTTTTGACCTTCCCGACCATAACTACTTCTCGGGAGTGTAGCGTGATACTGTTTGCTGCGCAGTATCGTCCGTCTATGAACTAAGACTCTACATATACAGGCATTTCTAGTGTGCTTTTTATCTTATAAAACATCTCTAATTCTGTTTGATTCAATGCATTAAGCCTATCATCATTCTTAAAATTATTAGCATTCGCATCAGCTCTCACATAGATGCATTTGACCTTTTCTTCGAGGGCATATTCCCGGAGTCTATTAAAATAATAACTAGCCACGCCTTTTCTTCTCAAAGATTCATCATGTACGTATAGCAATTCTAATACTATTCGAGACATGTGTCTTCCCGGAAGTGAGGGACTACCTTTGAAAAAATCCATCGAAAAGACAACCTTGTCTGTTCTTTCATTATAGAGACAAAACTTTACATCTCTTACGTTGCAATGATAACCTCTTTCACTTGTACCCGTAATGCCTTCATCGTCGAATTTAAATATTATATGTTCTTTATCCCTCTCGAGGCATTTTGGTAAACCCCAGTTTGTAACTAGATTTTCCATTACTTTATCATTATTCATTTCTATTCCCCTCTCACATCCAGAGTTCTATGCAAAAGGGAGAATCCCTTCTATAAGTTCATCAAAAACTAAGACTGTTTTACTGGGCTTAATTCTCTGAAATTGAAGTTAACAAATATTAATCAATAATATATACTTCATAGATAACACGCAGACTTAATTTTACAATTTTAATACTCAACAGTTGGGAGCGAGCACAGTGAGCAATATAACTAAAACTTTAAAGAGCACAAGATTATTCGTTAAAAACTTCAATTCAAGAATAAAGCTAAAAAACGACAATTTCAGTATCATCTCAAACAACTGCTGGGGCGGTCAAGTATATAAAAATTTAGGAAAACCGTATAACACGCCATTTGTTGGCTTATTTATATATGGGCCATGCTACATTAAGTTATTGGAAAACCTCGATTACTATCTTCACACACCGTTGACCTTCACTGATACGTCCCAGTATAAAGAAACTCCGAGCTACCCCGTCGGTCTACTACACGACATCGAAATCCATTTTATGCACTATACCGACGAAAATGAGGCCTACGAGAAATGGAACCGTAGGCTAGCCCGATTTAATTGGAATAATATATTTATAAAATTATCTGATAGAGATCTTACTTCGGAAGAACACGTACAGCGTTTTGATGCTCTTACATACCCTAAAGTGTTTTTCTCTTCTAAGAATACTCCTGGCATTAACTCCCTTGTCTGGTTTAGGGAATTTGAAAATTCCTCTACAGTCGACAATGAGATGCTCGTTTACAAAAAATACTTTAATGCTGTGAATTGGCTTAACACAGGTAAAATCAGCTAAGCGCGCCTATGCGTAGTCACTACCCACCCCGTTGTCGCTGCGCTTTTAATTACAAGTCTCACGGTGCCGGAGTCGTTGTATATCCCGAATTCATTCGTACCGAGTAGCACGCCATGGTCGTACGGAGAGGCGTTGTAGACACGGTTTAACTTATACACGGTCCCGCCGGACGACACTACTCTCGCCGTCAACTTTGGATAGTCCGTTATGCTGCCGAGCGCTATCACGCTAATCCCTGTTACCCCGGATGCAATGCTATCTCGCGTTTCCGTTACCGGGAATAGGCTCCAATCCGTATTGCGGTTACGGATGCTGACAACGTGCTTGATATCCTCAACCAACTCGACCAGCGCCGGTACGTAGCCCTCTTCTATTCCGATGCTTGAAGGGTGATTAACCCCGTTTCCGCCGTACGGCTGTTTAACCGAGTAGTCTCCGGCAGCATAAGCGCCGAACATCTCACGGTCAAGCAGCACCGGTAGATATTCCGGATATTCCGCGCCCCACACCTCAATTGATTTGACCAGTAATGACTCACCGGCGGTTCCGGTAGTGTACAACATATCGAGTGTTCCCGGAACATCCCAACAGTCAGCGTAATCCTTGATGATCCGCGTTTCGTTGTCGCCTAGCTTAATTTCAACAATTGGCCCTTGCTTAGTGATCGTTAGTACAACGTCAACACCTTCATAGGCCACGGTATCTGCATAACTTCCAGTAATGAAGATCGTATAATGTGCATTATCTGCTATCCTCATTGCGCTATCGATCTTCGCAAGATTGCTAGGAGATTTCGGAGAGAAGATAACGGCATTGTCATAAAATCCAGGGTTTGTCTTATTAAATTTCACGGTGAGAGAATGACCTGTGCTTGATCCCAAAACATGGAAGTTAAGCTTGAGCTTCAATTGGAAATCCTTCTGCAGATTCCCTGCGAGAGAGAGTGAAGCGCCATTAATAAAGGAATACGTTCCGTCACCATTGTCGGTAACCCCGTTGAGAATTTTATTGAAGTCTGATACGCTAATTTTTTTGAGCATCGGTCTTGTTAAATCCAAACCAATACGCTTGATATCTGTTATACGAGCAACGTCACAAACGTATGCTCCATACTCTTGCCCAATAGCTCTTGCAGCATTAGCTGCTGCATGTATAGATGAATGTGTAGTATACGTTCCCCAAGTTGTTTCACCGGGCAAATACGCACAACGAGGACTTGTAATAACTACGATATCAGGAATAACAGTAAAATTCGCTTTGACATAATCTAGCAATGTTTTTAAGTAATATGAAAATATTCTTGCCGAGTCATTACTAGCATGATTCATCCCGAAGGCTATAACAAGCAAGTCCGGCGCGGCATCCTTACACATATCAATCCAGGTTTTGGTTATCCAGACATTGTCAATTTGAATCGTTCTGCTAACTCCCCAATTGTTGATCACCTCTCCCCCAATTGAAAAGTTTGAGTATTTAAACGTGGTGTCTGGGAAAGAATTTACGAGCATTTCCATTAATTTGATCGGATACGCTGCGCTTTCTGCGGAAGCGTCTGGGCCATTAATATACCCCAGTGGATTTGAAGAACCTTTCACTGATCGAAGTTTTAAGTTCGCAGTGTCCCAACCTGCCGTCGAGATACTGTCGCCAAAGATACAAACCTTAACGGGCTGATTCTGTGAGATAGCTTCCGCAACGCGCCGGAATCCACCAGTGTCCACCGCTTCTGTCAACCCACGAACCGCGCTTGAATTGATTTTCCCGCTGAATCCACGGAACGTCTTTGAGATATGCGTAAACCAGTTAACGGGATTCTTTCTGCTAATTTCCGCATTACCGATTTTTAGCACTTTAGAAGTGCCAGAGAGTGCGCTATCCGGCACAAATGTGCCCGGCTTATCGAACATCGCATATCGAATACCTTTGTCCTCAAGGGCCTCGAAATAAGTGTTAAGCTCCGTTGTCTGGTCCGCGCCAGTCGGTTCCACTCCGTATAAAGACGCTTGGCCTCCGTACGCTACATCCCCCAACTGTTCCCCAAACTGCTTCTGCATATCCCGTACTACATCACCAGCAGCGGCAATTGTCCGGCCAGGCGTATAGCTGGGATCTGGCGTTTTGATGTCGGTCAGCTCCGGGTCTTTATCCTCACTGCCGCCGACGATGATCGTATCCAGACGCTCATCTACAAAATCGATAGCCTCTTGGATGTTGGCCGCACCAGCAACTGCACCTGAATATGTCACATGCGCAGCTGGATGAGCTGTGGTTGAAGCCTTGTGAATCGTTATATCGCTCTGTGCCCCTGTAATCCGCCCTTCGTGATCAGTCAAATCCGTCTGAATGTCGGCATAGTTATCGTTGTGCCGCTGGAGATTAATTAAATCCAGCGTCTTGGTAATCATTCTCCGCGCAAATGTCATTTTTGTAGCAGCTCCTTTCTAATAGAGATATTGATAGCGGTAGATCACTTCAACAGTGATATTGGGGCTGGTGGCCGTCACAGTGAATGTTGTCTCCCCTGGTTCAAGAACAAAAAACACACCATTGCTGCGGGACCAAGCATTCACCCCATTAAGCCGCACCGAGCATTTATCCAGGTCGCAATCGATCTCAAATACATCGTTAGTTCCAGCGCTGCCGGTGATGGTCAAGGTCTGGATGCCATCACTCATCGAAAGGTTTGTAAACGCCCCTGTGATACGGATCAATGGGTAAGCCAAGGTAGAACCTTCATTGTTAACGGTAAAGGTCTGACCGCTTGCTGTAATCGAGAACGAAGAATCGGAGATATAAAAATAGCCCTCCCCAAAGGAAAGGCCCTCTCCATATTCCCGGAGCTCGGTATCCTGTATCGACTCGATCCACGAATCATCCATCTTCATGGGCACATCAATCTTCCGATTTCCCGTCGAAGTATCGAATGCCATAGAACCGCGATATTCAGCGATGAACCTCTTTTGCGGAATATCATCAAAGATGACGATTGCTGGGCCATTCTTCACATCAAATACACGGGCCAGATTCGCCACAGTGCCGTAATAATCGTCACCCATGATAAATAGACCCAGGCCGAGAGGCCGGGCCGCATAGGTACTGCCGAAGCTCTTTACGCCGTCCCTGCCGGCAAGCTTGATGGTGTTCTCCTCGGTATCCGGCAGGGGCGGTAGGTCACGGGAGACCAGCAGGATGTTCAAGGTTGAGAGCCAGACACCGTTTACTGATACGTCGTTCATCCGGACTTCACTCCCATCGTTTGCATCCTCCGAGCCGTCTTCTCTCGTTCAGAATAAAGGATTTCCGTGTCTGCCCGGTCTTCCAAGGTTACGCCGTTTACGGACATGTCGATGTGGTTCTCGACTTTGGTTTCGGACTTCGTCACACCCGCTGCAGCTCCGATAATGCTGGGGTTATCCAGGATGCGGAACAAGCCATTGAGCTGCGCAGTGTTAAAGATTGCTTCCTGCCCGTGTGCGATAATCGGTACGGGGGCGCCGGCAGCTCCCGGGATAATACCACCAACATCGAAACTCTGCAGCTTATCGCCAGTGTCCTTGGTAATGCCGTACAGATCGCGAAGCGCTTGATTCCGAGAGGCTAACCTCACCATTTCAGTACGGTTACCTGCTGCTGCAGCTGCGGCATAGGCATCCTTGTTGGCATTGTACTCAGCAAGGTCAGCATCCTTCTGAGCTGCTTGTTTGGCAGCAGAGATTGCTGACATCTTCGATTGGTACTGAATGATGAAGGCGTCTAGATCAGTCAGAATCTGCGTATTGGCCGTACCAGCGGAAGATACCCGGAAAGCAGCGATGCCCGCTTCAATCACCTTGATGTCATCGGAATAAGTATCAAAGGCTTCTTTTAGATCATCATAATGGGCTTCGGTTTTATCCTTCTCATCCTCGAATGCCTGCAGCTGAACGTCCTTCTCATCCTGCAGCGCGTCCTTCTGGTTGTTCAGGTCCCGCTTGCGCAGGTCGCGTTCGTGGTCCTCAATGAGTTTGTCGCGCTCTTCAATGGTCTTCTGCCGTTCCTTAAGGCCATCCTTACCAACGGCAGAAGCAAGCAGATCGATGCGAGCGTTCTTCTTTGCGAGCTCCTCTTCATAATCCAGATCACTGTTCGCTTCAGCTTCCTTCGCAAGGAGATCATCAATAGCCTTGATCTTGGCGTCCTGCGCAGTAACATAAGCATCTTTACGGGATTCAATCGCAGCCAGTTCAGCCTTCTGGGCCTCATCAATTCGGTCCTTCTCGGCATCGACCAGTTCTTTGGTCAGATCCAGCGTCTTGTCGGTCAGGTCCTTCCGGGACTGGTAGAGTTCCTCATCCGCCTTCTCGTAATATGTTGTGTCGATGGCATATTGATTTCGCAGGTCCGTCCAGGCTTTCACCTTATATGCGGCGATCTCCGCTTCGGTGGCTCCGGACTCTTCTAACCGGCGGGCTTCCTTCTCAATCAGCTTGGACCGCTTCTCGTACAGTTCGCTGATCTGCGTCTCCGTCTCGGTGGCAACTTCCTTGCGGGATTGCCGGACCTGATCATCCGCTGCCTTGTACTGCTCAGAATCTTTACTGTAGCGATCCCGCAGGCGTGTCCAGGAGTCCAGTTTCATCTGAGCAATCTGCAGTTCTGTCTTCCCGCTGTCCTCCATCCGTTTGGATTCAGCATCAATCCAGGTGGCAGAAAAGTCATACCGGGACTTGACCGAATCCTCACTCAAACGTTTGAGTTGCAGGGTCAGTGTGCGGGCATCATCCACAGATTCAGCCAGAAACTTAGCATGCTTTTTCCGGAGTGCCTCGTACTTCTCCATCTGCTTTTCAGCAGTGAGGTCATAATAGTCAGCCTGGAACTGAATGGTCTTCAGGTCAGCCTCATATGCAGCCTGGCGAGCTTCGGCAGCAAGCTCAGCAGCTGTTTTTCCGGTGGCTGGTTTATCCTTCTTCGGCTTTTCCGGATCAGTCAGATCAATGCCTGGACCGTTTGGACCATCCAAGTCAAAATTACCTGATGATAGAGCGGCGGCGGCAACTTCAATTACCTTTTGTTTCTCCGCCAGTTCCCGCTGTTGATCTGTCAGTTTGGTCAGTTCTTTTTCCGTCTGCACCTTCAAAGTATTATTCACGATGTCCATGACGTTAGGAGTCGTCCTCTTCGCTCTTTCCTCGTTTTGCTTCACCGATTCAGCAAATGTGGAAGCTTGGACACCATTGACCGCATTCATAGATTTTAGGAGTTCACCGTAATTCTTGATCTGAGCCTCAACGGCCGCTTTCTGTGCCGCTGTCTCTGTCACCAGAGCCTGCATCCGTTTACTTGCTCCAGAGATAGCCTGATTGGTAAAGTATCGGTCTGACTCGATTTGGCCCTCAATAACACCGATGTTATCCGCTCGAATCCGTCCGTCTTCCTCTTGGACAGCATTAAGACCAGGATACTCCCGTTTGAGTGCGTTCGTAGCATCGACGAGCTCCTTCTTCTGTGCCTGATCCAACTTCTGAGCTGAGGAGAGTTTTTTGAAGGTAGCGAGCGACTTTTCCAAAGCCTTCAGCTTGTCGTTCTTTGCAGCTAGGTCAGAAACTTCCGCTTTCTGTTCTTCAAAGAGAGCACCCACAGAACCCTTAATCGCCGTGTTCATTTCCTTAAGCTTCTCAGTCGCCTTTTCCGCGCCATCGAAGCCCATGCTTCTGAGATTTTTATCGATCTTTTCCAGTTGCTCATTGATGTCCATTGCTTCGGACAACATCTGGGGATTCCCTTGACCGGCATCAGCCTTCTTTTGAATCTCATTTAGCCGTTGTTGCAACTTCTCGCGCTCATGAAGTGCCTTGGTAAGATCCTCCGTCTTCTTGCGGAGCTCGGTCAGATCATCAACGGAACGCTTAACAGGAGAATCATTAAGAGTATCGTTGAGCTCCGCCTGCGCTGCTTCAAAGTTCTTAGTAGCCTCCTTGCTCTCATTGTACTTCCCGACGAGAAAGGCTGCGCCGGCAGCGACCGCTCCAATGGCTACAGCTAAAAGCCCTAACATTGGGATTGTTCTTGCGGTGAGTGTCCCCGCCAATATCGCGGCTTCGTAGGCTATTTTGACAGCATCGATGGCCTTTTTGAGTTGGTAAGCAACGACTACGCCTCCAAGCAGTAACGGTGGTAAAGCCGCAAAGGTAATGAGCGCAGCCTGCGTTGACTTATCAAGCTCGGAGAATCCGGTGAGTAAGGCGGTGATACCTTCAACCGCTTCCCTGACTGCCGGCAGGAACATGTCCCCGATGATGATTCCAGCAGACTCAAAGGCGCTGCCCATGTTATCTGCGGCGCCCTTCAGGGTATCCATCTGAGTTTTTGCAACACGTTCTGCAGTTCCGCCTGCTTCGGCAAGGGAATCGGTATAAGCATTGAGCTTGCCGCTTCCAGATTCAATCAGCGTAATAAATGCAGATGCCGCTTCGCGCCCGGCCAGCGTGGCAGCTACGTCAGCCTGTTGTGCCTGGGTCAGCCGCGGCCAGATCTCTGTTAGTTGTTGGACAATTCCGGATAACGGAAGAATATTACCTGCGGCATCTTTAATCGAGAAACCCAACTTATCCATATATCCGGCAGCTTCTTTGGAAGGAGAAGCCAGCGCCAACAGGATCGCCCGTAATCCGGTACCCGCCATCTCGCCTTTAATGCCGGCATCAGACAGGGCACCAACAGCCGCAGTGGCCTCTTCGAGAGACAGCCCCATGGACTTGGCAACCGGGGCGACGTATTTCATCGCCATACCCAGGTCAGTCACATCGGCATTGGTCGAAATACTGGACGATGCCAGCACGTCCACAACTCGAGTGGTCTCAGTAGCAGCCATCCCGAAGCCGCGCAGGATGGAAGAGGCAATATCCGCGGTTGTGGCCAGATCAACATTACCTGCTGCCGCCAGCGACAGCACACCCGGCATTGCCGCGATAATCTCCTTCGTGTCAAATCCTGCTTGTCCCAGCTCAGACATTGCGTCTGCGGCCTGTGAAGCCGAGAACTTGGTCTGAGCACCGAGCTTAATCGCATTGATACGCAGAGCTTCGAAGTCAGCACCGGTTGCTTCCGTAATCGCCTTGACATTCTGCATGGCCTGTTCGAAGTCAGCTGCTGTCTGTACGGACTTGGCAATCGCAGCTCCAACAGCAATTGCCATGGCTGCATATGCAGCTCCAAGTGATTGGATCTCAAAATCAACGCTACCGGTTACTTCATTAAGCTCTTGCATCTGCTCAATGATGTCATCAATGACTGAACTGCTGACTCCGAGATTCTCAAGCTCCTCTCTTACACTGGCAAGTTGCTGTTCAAACACTTCAGGATTCGCCCGGCGGATCGCTGCATTAATGTTGTCAATGTTCTGACCGCTGGCACCGACGTCCTGCAAAGCCATATTCAGCTTCATGAAGCTCCCGGTTGCCTCGTGAGCATGATTGCCCATCTTTTTGGCAGCATCGGCTGCACCAATTGTACTTTTCTCAGCCTGACCCATGCTTTTATTGATCTTGCTGATCTGTTCTGCACTGACGCCAGACTCTGCCAGCGCCCTATTCAGCGTTTGAAGGTCCATTCCGGCCTTCTTGGCCGTCTCCCCCATACTGGCGAAATCCTTCTTCACTTCTTTGATGTCGCGCTTGATCCCATTGGCATCGGCAGTCAGCCGCGCCTTCAATTCCCCGAGGTTTCCTCCAGCCACTGATTATCCTCCTCCCTTCATGCGCGCAAGCTGCGCTTGATACTGGTCTTCTGCGGAAGCCCGCGGCTTCTCCGGCGCTTTCGGCAACACTTTGATATAGCGATTAATGATTTCCTGCCGGACTTTCTGGTCCGTGATATGTGGGTAAGACGCAATCTCAAGCTGAGCAATCACTTCCGATGCACGAGCCTGATCCTTCAGGAGCAGCAGCTGCGGCAGATCAATAAAGAAGTACTCGTTCTCGATCTGATGCTGTGTCTTATCCAGCACCGTGCAGCAGCGTAAAACAAAATCGTCATAGGTTAACCCTGGGCCTGACTCTGACGAGCCGCGATTGAGGTCACGAATTGCTGAGCCATCGGCGGAATCAGGCCGCTTAAGTTTTTTAAGGCTGTATTCATGTCGTTCTTCTGCCAAGTCAAATTCAGGTATTCAGTACATTCAGCCAGGCTAGCCTGCTCACTGAGCTCATTTATGTCGATATCGCTCATGAGCGATGTGAGTTCGTATATCTCGTCAATCATGATCTCGGCTCCGGCTACGATCATTACAGATCGGTCAGCTTCCGGAGTAAGGAATATCTTTACGAGCAGATCACCGATCGTGCCGAGGTGGTCTGTCAGCTTCTTCAGGCGGTTCCTGGTAAGCTTCGGTATGGACACCGTGCGGCTGCCGAGCTTCAGCTTATCTTTTCTGGTAAGTGGAAACACGTTCATCCCTCATTTCTCGAAATACAAAAAAAGGAGAAGGCACAATGCCCTCTCCCAGAATGGTTCTATTCAATTATGATTTACGCTGTGGCGGTGATATCGCCCCAGGTGTAGAGCAGGCCCTTTGGTGTGGCATTAACATCCGGATAAGCCATAGCAGCCACAGTCAGCCGCAGGTTGTTATCCAGGACGAACGCGGCGTTCATATCAAACTTGATGCCGACACTCTCGATGTAAATGAACCGGGAAGGATCAGTGATACCCTGCGGTTTGATAACCGCTCGTTTGCGAGGCAGCTCCTTACCAGCCAAACCTGTGACCTGATACTTTACCTTTGCAGGGGTATCGCCGTCTATAACCTTGGATGCATTCGGGTTATACGAGACAACCTTCTCGAAGTCCATATCTGGAGTCTCAAAGTTGATCGCTCCTGTGGTACCCGTGACAATGGACTTCACCGGCGCAGTACCTGTTTGGTCAACGGTTGGTTCGAAGTAAGTTGTGGTCGTTGTGAAATTGATACCGCCCTGGGTCAGGTCGATGGTAATAGCATCAGATTCTTCAGTACCATCCGCATTAATCCCCCAGGTGAAAATGCCGGGGCCAGCGTAAATATTATTGATATCACTCATGAATTAATTCAGCTCCTCTCTTATGATTGCAAGCTCAGAACACCCACAAGGATGTCTGTGCTTACGGAAAAATCGACATGGACAAAGCCGCCCTGGTTATACAGTTCGGCATCGAATGGTCCAATGAAGCTCTGATCACCTGCAGGAACAGAAACAACCTTCTGCCCGGTGCGGCCGTGTTTATCAGTGGACATCGGGATCGTCACATTCACCGCGCTGCCGGATCCATTATCGACGTACAACAGTTGAGCACCATTGTTCTGAAATTGCATGTCATCGGCGGAGTTCGCGGCCTGCGTCGCCAATTCTACTCCCGCCAAACTAGCGGTTGATCTCGCTATTGTGGCTCTAGCCATGATTATTCCTCCCTCGCGTAAAACTCAAAATTGGTTGAATAGATCGGCCTGTCTTTCTCATCCAGCCCAATGAAGCTCGGCTGCATTGTGGCCACGCTGGAAAAGACATAGGTGCTACCGACCATGTAATTTGATTCTCGGTGCAGTAGCTTGGACAATCCCTTCGCCACAGCTTCAGCAGTTGCCATGTTGACCGGGTTTGCCTTGTAGGACTTACCCTTGACGATAATCTGATAGGACGGCCGCTCCGTCGGAACATAGTCATCCGGTGGAGGACCGCCAGAGTCTTCAACGAAGAGGCAAGGAAACTTTGCCTCAGGGAGATCTGCAGGTACAAAGTTAGCATCCGGATACACGGAGTAGCCCGCGCCGGTCAGGAAATTGATCAGATCACTTGCGAGCATGGCATCACCATCCTTCCAGAATCTTGGACAGCTCACTCTTGATCAGCTTTTCGTTCAATTTGATGGCATTTGCAAGGTACTTCTTGCCCGGCATATAACCTCTGTAATTACCTTTGCTTAGGGTCTTCTCCCCAGGCTTGAGTGTGATCACCTTGCCCAACGAAGATTTGTTAAATCCCTCATGCTGGATGACGGAGTAATCATTCACATCTACAGTAGCCCCGAAGTCGATGGAGGATAATCCGATTAGCTGAATCAGCTCCCCCACTTCCAGGGATCCCTCCAAATCGCCGCTATCATTAGGAGCCAGCCGCTTTGCATCATGAATGATCTTCATAGCCAGTTTGGTCAGTGTCGCATCAAGGCGGATTTCGATGTCCTTCTCCAGATCATCGAGCCGGTCAATGATTTTGTCCAAACCGTCCAGCTCAAATGAGAACGCGCCATTATCAGCCATACAGAACCACTTCTTTCACATCGTCAGTACCGAGATACTTCCGGATCTCATAGTGCTTTACGTCGATCCGAATCTCCGTACCTATCGCATCGGTGTAAAGTAGCCAGTCATCGAAGCCAACAGCATTGATTCCCTCCAGGTAGACGGTGTAAGCGACCGTTATCTCCTCGCCCTTGGCGTTCTTAACGAGCTTTTGCTCCTCGACCACCTTGGCATCCTTCTCCACCGGAACGGCTGGCAGAGGGCGGCCCCAATCATCGACACCGGGGTGATAATGGGAAACGGTCGCAGGATATCCGAACAGACTCATATCAGACACCCGCCATACTGCAGGTCGGTTCCGCCTTCCTCAGCCTCTTCTTCTGCAATCTCGCTGGCCGTCTTCCCGAGCAGGTCCCGCACGTCCGGAGCCACAACATCACGGATTCCGCTGTACGTGACACCTTCGCCATGGTCATCGACCGACTTGACGCCATGCTTCTGGAACTTGAGCGCTGGGTCCAGCCCTTGCATTTCCCAGATGGATTGAAGGGCAGCAATCTCCACGGTCAGGATGACGGCGGGATACCACCGGGCAAGGTTACGTTCAGCTTGCTTTACAGCCAGTGGCTGCTTCAATGGCTTCTTATCCCATGCTTCGGTATCGAGGACATTCTCCGCTATCCAGAGGTTGACCTCTTCGGTAGTGGGCATGACACATCACCTACTTCTTTTCAGCTTCTGCAATGGCCGCAGTAAGTTCCTCAGCTGTCTTGGTGTCAAAGCCTTCAATGTCCAGCTTAGCAGCCTTAGTGCGGAGCTCCTGCAGTTCAGCTTCTTTCTCGGCGATGGCTTCCTTCAGTTTTGCTTCACCCAGACGGCCAGCCTGCGGCACGCCGAGCACCTTTGCCCGTTCCCGCAGTGCCTGCAACTCGGTGTCATCCTCTGGCAGTGGTTCGACTTCCTCAGCATATTCCTTAGCAATCAGATCCAAGGCGATTTCATCATCCACTTTGCGGACAATATCTCCCGGCTTCAACCACTTGCCGCCGTTCTTCACAACGCCCTTCAGTTTGATATCCACTTTATTCACCCTTTCCTCTACGTGATGTTACGTGATAAAAGAAAAGAGCCCCCGGGGGGCTCCTAGATTACAGTTGCACTCATTACAGAATCCGCATAAGGGAACGACGGGAAGGCCAGGTTAACACCCACCGTGCGAAGTCGCAGTGGATGCTTGCTGACCAGGTCGCGGAATACATAGATGCCGTTCTCTGCAGTCGTTTCCGCTTCGATGCCGGATACCATGGATTCGGTTGTCTCAGCCCACAGGTAGTCACCCAGTTTGCCGCCTGGCAGCATGACAAACCGATCTTCCGGCGTCATACGCACCGTACTGTAACTGGTCTTGCCGTTTACCAAGGCAGTGTCCTCTGTCCGGGCAACCGTATCGTAAGCAAGAATACGCGGCAGCTTCATGCGGTCTGTGATCTGGTCCAGTTGGCTCGAATCCAATTGTGGTGGCACTGCCGTCCCCGTTGGGTTGCCGAAGTAGAATTGCCGCATGGACAGGTTGTTCAGCAGGTACGAGAGAACAGTTTGGCTAGTAAAGGCGCGTTCCAGGATCACCCCGCGGGCTTTCTGGATGTTATACCATGTCTGCATGTCGAGGAGTGGAGTAGAATTCACCAAATCGCTCCATCGATCAGTACCACTTAAAACAGGTTTTTGATCATTGGTAAAACCATAGTCAACAGTAATACGGACATCGTCCTCGACATAGTTTACAGCACCAAGGCTCGCTGCCTGCATGGCGATCCACTCTTTACGGGCCCGGATACTGGATACTGCATACTTCGCATCATCCAACTGATCCCGCACAATGCTGGCAACTTCCTGTCTACGCAGGCCGGATGCCTGGCTTGCCATGAGCAGCAAACGGATCAACTTCTCATCCATCCAACGGCCGCGCTGAATCTTAGGAATCTCAATGCGCTGTCCGGATGTACCTTCACGGGAACCGTACTTAGTTTCAGTCCCAAGGTGTGCGATCTGTGCCATGACTGGCAGCGAAGATGCCGACTTGATCACATCGACTGTCAACTCATCCGTTTGCAGCGGTGGGAACAGGATATTCTGCCAGTAATCATTCTGAATCGTGAGGTTGGACGCATAGACCAGCAATTCCTCCCCGGACAACGCCTCTTCTAACAACAACAGTTCTGGATCCATATGTTATTCATTCCTTTCAAGTGAGTAGAATTGGTTTATGCAAAGGTGATGCCGGGCATCTTGGCTTTCAGGGCAGCATCAACGGTAACGGCCAGGCGTGCAGAAAGTAGCTTCGCCACTTCGACGCCGCCGATGACATGGTCGCCATCCTTGACATTTGATGTCCGGACTGTGATGAACGTCGGGTTGTCACCGCCGTCGGCATTGGTCAGCACACCGTTAGCTGTGGTATAAGCATTGGTAATCGCCGTGAAGGTGATCGTCTTAGTACCGGCATTAATCGCGGTGATGGTCTTAGGCTCGGTGTTCGTACCGTTGTAGAAGGTAATGATATCCCCGACAACCAGCCGACTGACGTCATTGAGCACAGCTGTAGTTGCGTTTGCTGCGACGTTGGCCGTAAGAGCGAGCCCGCCGGTGTATGGACGATACTTTCCGGATGCCGTGATCTTTGCCATTGGTGTACCTTTCTTGATGATGCGATCACCGTTGGCATCAGCAGGGACCTTGGTGTAATCAACGGTAGCGCCGTTCGTGATAAACCGGACGACTTCCATCGATGCGAAGATTTCATAATCGCCTTCCACTTCAAAGAGTGGACGTGGTTGTAATCTCATAACGAGTATTCCTCCTTATTTTTTTGCCCAAGGGTCATTAGCAGCTGCGGTTGCAGTGCTGTCGTTTTGGGCCAATTTCTTGATGTTCTCAAGTGCGGACTTCTTCTGGTCCGGGGAGTTCGGAACGGTTGCACCAAATCGGCCAGTGCTACCAGCCTTAGCCTTCAGCAGGTGCGGCTTCTTCTTTGCCAGCGCCTCCAGCGCTTCCTTGACGCCCTCCAGCTCGCCTTTGTCATTCTCCTTGACGGCGGTCAGATCAGACAGCGCAGCAGCATCCTCCCAATCGGCAAACCCGAGTTCGTTCGCCAGTACCTTTACCTCGGCATTTAGCAAGCGTTTGAAGGTCTTGTCGTTCTGTTCCTTCTCACGCGCCTTGATTTTGTCCTCGACCAGGCGGTCGACTTCAGCGGGATCAAGTTTCCCGTCTCCTTTTTCTTTGTCCTTCGGCTTAAGGGCTGCCTGCATGGCTTCGACTGAGTCGTAGCCCAGATCTTTAGCCAGCGTCTTCTGCGCTGCCTTCTCGGCGCGGGAAAGGCGTGACTGAACAGCAGCATCAAGCTCGGCCTGCGTAAAGGTTTTACCTTCCCCTGCCGCTCCTCCTTCACCACCAGTCCCGCCGCCCTCGCCGCCTCCAGCTCCAGCTCCACCTTCACCGCCGCCACCGTCCGGTGCGAAGAATTGATGAAACCGTGGAAACCGTCTTGAAATATATGTGTACATGTTGTTGACCTCCTGTTTAAGTCCGGGTGGACTGCCTGCCGCAGCTTTTAGTGTCGTCACGGCGTTTTGGACAAAAGAAAAAGCCGCTCGGTTAGAGTGGCTTCAGTTCACATCCGCAGAACGGACAATATTGAATTGATGTTGATTGATCGAAATCAATCCGTAAATCCCATTCCTTTTCCTGTTCATCATAAGTGATATCCACCCAGGATGAAGGAAGGTCAGTACATTTATGCACGTTCAAAAATCATCCCTCCCTCATCTGGATCATCACATCATCCTTGCCGCATTCCAGCAGGCCGAGTGCTTCAGTGTTCTGAATATGACTCCAAACCGTCTGAATGCTTCCATCGGCCAACTTCACCACAGCAACAAATGCCTCAATGCGCCCTTGTTCGGCTGCCTGTTGTAGGCTACCTGCGCATGCCAGGGGAGTGACTTTGCCTGCGCGAAGGTCTCGCCGTTCCTTGATCTCATCCAAGGCAATCAGCCCCCCTTCTTCTTAATCTCAATGTTCGCCGCCCGGTAAAGCTCCTGCAACTCCCCGTATTTCTTCGTTCCCCGCACCTTGTTACTGGCGAACTGCTTCAGGTCAGGAGTATCATCCGGCAGCGTGGCCTTGTACCTGATCCATTGTTTCCGGGTCTCATTCTTCCGTGACTTCTCACGCTGCAGCTCGTTGTATCGCTTTATGTTGGCTTCGGTGCGGCTTTCCTGTTCAAACGATCGATTGCTGTCCTTGATGGTCTGCTCGACCTCAGCAGCAGGCGTATATTCTTCCACCCATACCGACAGGGAGTGAACACAATGGCTATGATACGGCGGCCGCAGCTCCAGCTTTGGGAATCGCTTGTCTGCTCCGCTGATGGAATAGACACGGCCCTGATACTTGGCGCACATCGAACAGGTGATGCCGACAGAATTGACATACACCAGGTCCTGTCCGTTTTGCACGGCCATGTTCTCGGTACCGGTGACATGCGCCTTGCGCTGATGGTACTGCACAACGCCAGCCATGTACTTGTCAGCAGGAATCTCAGCACCGTTCTTAGCAATCATCCCGGTGATGCCCTGCTTATTAACCTCGGCAACGGCATTCTTCGTGGCTTGCCTCCGGCTGACGCCCTGGATCAGCGATTGCTCATTCGCACGGCTAACGGCAGTTTCAATCCGCCGTTTGGCATCGCGACTCATATGCTCCGATGCTTCAAGGATGGAATAGAATCCCTCGTCTGAGATCGTCTGTGCCGCCTGCTGGTGGATGATAATCTTAAGCGAACTGTTAACCGCTTCAGCCGCTATCCCCGCTGCCGTCATCTGCTCAACCGCTATAGCAGCCCCGTTACGGTATTCAGAGCCAACCAGATCAGCCAGACCTTGCCCGGCGCTACTGGTCAACTCCTCGATGATGACCTCAACCTGCCGAAGCAGCTGCTGCCTGCGGCGGTTTGATATATTGCCGACCTCCAACGATTGGACTAGGGCTCTCAGGCGTTCGTCCGTCAGGACATACTGAGCGATCAGTTCCTCCGACGTAGCCATCCTACACCGTCACCCGGGGCGGCTGCGTGTAGGTTGGGTTTAAAGTGTCGACCGCCTTCTCATCCTGAATCTTCTGGATCTCGGCAGCGATTGCTTCCTCAGACCAGTCTGGATGCATCCGGCGGACCGTGGTTTCAAGCGATTGGACGCCATCGACATACTTCTTGCTCTCTTCTTCGTCCTTCTCGCTCTCAGCCTTCGGCAGCATGGTTCCCCACTCAATGACCGGGTTAACAGGCTTCAGCCCGCCCTTGCCGATCGCATTCTCCAGCAACATGCACTTCCGGATGGCGTCCTTGATGGCCCCGTCGAACTTCGCTTGAATGGCTTCGGCCTTGATCACCGACTGAATCCATAGGTACAGCAGCGCAATGCCTGTATCTCCCTTGGCATCTTCCAGCCCGGCAGCCTGGACAGAAGTCTTCGATACGGCCAGCAAGTAACGGATCAGACGCTCTACATGCTTGAAGGATTGGTCCGTCTTCGCATCCCAGGTGATGTACTGCGGGATGGCCCCGGTCTTCTCATCGAAGGAAACAACCTCCAGATCCGCTCCGCGAACAAACCGAGCGCCGTAATCCCGCTGGTTCTGGTTGGCAACCGTGTCCCACAAGGCCCGGGGGATCGCCAGCTTCGGCTTGCCGTGCTTGTCGAAGACGATGGAATCACGGGTGATGGTCCAGTTGATTTCCTCCTGGATGGTGTCGATGTTCCGCAGAGCCGAACGGCCCCGGGGATGCAGCAGGGTTTCATCGTTGATCACGAAGCCACATAGCAGCTCGGTGACATCCTTCAGGGTTTCGTCATCCGGGATCTCGATTTCATAAGTGACAGCATACTGGTTAATATCGATCTGATCACCAACAGTCTCGCCGTCCATCTCATAGACCTGCTGCTGAATGGTAAGCCCTTCGTCGCTGAGCTCCTGCCGTTCAACCCGGAGAAACTTCAGCTTACTGCCTCTGCGGTCATCCCACTCCTCGATCCAAGCCAGATCAGCCCCGCTCCCATCCTCATGCGGAAAGAACCGATCACCCAGCACCCATTCGAACCAGACCTTGCCCTTGGCACTCCGCCGGATCCGGTAAGCGATAAGGCCATCTACTTGATGCTGCGTGATTGCCGACCATATCTTGTCATTAGGTTTGGAAGCAGTGACCACGGCGGAAACAAACTCCAGCTCCGGACCAGCCTCCACGTCCGCCGACACATTGCCGAGCGCACGGTTGATCAGGTCAGCCGGCACTTCAGCCACCAGGCTGGCAAAGTTGACCACAACATACTGATGCTCGCTTGTAATCTTGATGTCTGCGCTCATGCCGCGGCGAATTAAACCCGGCCGCGACCGCCGGAAAACTCGCTCCGTGGTCTGGATGCTGCGAGCCCGCGGGAATATCTGGTCATGATCTCCGCCATAGAGCAGCCGGTAGTAATTCATGTCCTCGACCTCGACATCATAAGGCGGCGGGGGGAAACGCTTCTTGCTGTAAATGATGGTCACGGTATTTCCTCCTTTCTTGGCAATAAAAAAAGCCGCTCATTTGAGCGACTATCTGAATAATCCTATTGGTTTTCGTGCCCAGTTCCGGTTTCTAAAAGAGAAGTGTCTATCGGAAAGTATTGAACCAAGCCTTTGCCTTTAACTAACCAGTCTTCTTTGCCGTTTTTACCGGATAATCGAAAATATAAAGGAGTCTTTTTATTATTTTCAAGCAATTGTTGATTGGCTACTACTATAAAACAGTATGCAGGTGAGAACTGACCGCCTTTGCTGTAGGTCCGAATGATAACTAAATCATTATTTTTTGTTTCTAAAAACTCAAATTTCGTTAGTAGATCACCTATTTGTTTCTTAGTTAAAGCCACATCTGTGCTCGCCCCTAGATGATCTCTCTCGTAATCATGAGCTCTGGTTTCTAAAATGAAACTGTGATCTTCTGCGCCATTAAAAAACTCTCTGGCCCACTTCTCCCCCAGTTCATATTGAAATTTGTTCTTCTTAATAGAGTTCACCATTTTAACTTCCCTCCAATTAATTCCATTGTAACAGAATCACCAGCCTGAAGGGCGTTGATTTGAATATATCGACTCTGGCCGTCTAAGTGGCTCAGCCGAATAGCGAAGCGCAGCCATTGCGTCATCAAACACATTAACTGGCTCATCCAGATAAAGCCCTGTCTTCTTGTCCTTCCGCCATGACCACTGCTGTATCTCCTTGATGGTATTGACGCAATCGGGATGAATGTGTATCTTCCGCTGCTTCAGGTAATCGATCTGAGCCTGCACGCTGCCGGGCTCCTTCATTACACCAGAAGCATTGTATCCGGCATTCTGCCACATCTGAATGCGGTCAGGCTCGGCGGAATCGCAGTACATCGCCAGGTACTTACTAAGGCCCTGCCGATCAGCCAGCTCAATGATCCCGTCTGTGGCCATTTCATGGACGTATATCTCGTTGCATACAAAAAACTCACCGTCTTTGACACCGACCGTGAGAATGGCATTTGCATGGTTAAATCCAAAGTCCTGCGCATGATGCATGCTGTCGAACATCCCGAAGGAAGTATCGAAGTCATGCACAATGAAATTCTTGAAGATCAGGCCGCCGAGCTCGCCCCATTCTCCCAGCCCGTAAACCTCGTATCCATCCGGATCCTGCTCCTTACGCATCATCATACGGCGGTGGTAGGCTTCATCGATGAACCGGTTCTGCAGATACGTGGAATGGTGCGTCAGGATATCCGGACTCGAGTAATCGAAGTATTTCCTCTTAATCCAATGGGAAGCCGACACCGGGTTGAAACTGAAGGTGATCTGATAATAGAGATAAGGATTCAGCAGAACCCCGCGCAGCCGGTCATCCAGAATATCGACATCAGATTCCTGCAGCTCAGTTGCTTCCTCCACCCAAATCCAGACCAACTTCCCCTTGGTGAAGGTGATAGATTTGACCTTTTCGCGGTCCCGCACATCATTCATGCCGCGGAATATGATCTCATTACCGGTTACCCGGCTGCGGATCATCAGCGGTGAACGAAGGACTTCCCAGTATTCATCAGCCTGATCACCGTAAATCCGGTTGATCGCGCCGACCAGCTCCGCGTAGGTGCTATTCCGGTTGGTTTCATTGACCTTCCGGACACACAGCAGGTTGGCACCCTCATACTTCGGATCGCCAAGCTTCAAAATGAAGTCCTGTGCTATATTAACGGATTTGCCAGATCCGGCGCTGCCACGCATCACCCGGTACCGATGCTTAGAACGGTTAATGATCTTGAAATGAGAATTGAACGCCACGACTACCGGAGCACTCAT

Protein sequences of DBSCAN-SWA_6

>NZ_CP009285|5399383:5440013|5430411_5430747_-|WP_042215778.1|DBSCAN-SWA
MARATIARSTASLAGVELATQAANSADDMQFQNNGAQLLYVDNGSGSAVNVTIPMSTDKHGRTGQKVVSVPAGDQSFIGPFDAELYNQGGFVHVDFSVSTDILVGVLSLQS
>NZ_CP009285|5399383:5440013|5404237_5405416_-|WP_042215720.1|DBSCAN-SWA
MSSFKRIGFIVLDSVGIGEAPDAANFGDTGSHTLGHILERVPGLKLPNLQQLGLANIAPLPPLEPVADPTGYYGKMQEVSVGKDTMTGHWELMGLKIEVPFNTYFDGFPAELIEKFEAATGRKVIGNKPASGTEILVEYGEEQMKTGAWIVYTSADSVFQLAAHEDIIPLEELYSACRIARELTMAPEFSVGRVIARPYIGEPGNFVRTPNRHDYAVKPPEPTVMNALEDIGKDVIAVGKINDIFTGEGVTASYPTKSNEHGIQITIDELRKPFNGFLFTNLVDFDSLYGHRRDPEGYGRALEVFDQALPELLSTLSEDDLLIISADHGNDPIHAGTDHTREYVPLLIYSPKFKNPGSLGIRLTFSDVAATIADNFGAKAPQYGTSFLSELI
>NZ_CP009285|5399383:5440013|5414868_5415159_-|WP_042215749.1|DBSCAN-SWA
MIIQNESSYEGSFLFPREEVIPLAKVINLELSVNPSNPVQEAVAVVLLLINSHPGRQYELLQQIDMQIGEALAALDEARMKAADSKVAEDLESPVD
>NZ_CP009285|5399383:5440013|5414280_5414496_-|WP_042215744.1|DBSCAN-SWA
MPRVSLFELLRKIPAIKKKEAELEEKEQEVKWAIRRYEDLDERHKEVVRSNGFAGAFIYDHSTKEGENYAR
>NZ_CP009285|5399383:5440013|5407869_5408310_+|WP_042215728.1|DBSCAN-SWA
MTLLLDSRTSQNASFASSLGVPFPAILSPQLYGQVGLNIVRPTGNIRVEFFTTVSILLPAGTPPTGIFVIIVRGTTTNDPIIYSALEVSLPSNTNEQVLPITVIGSDFNVPAPENNQLIYSAFVSTTTLGPVRIGPESFTVTAYSD
>NZ_CP009285|5399383:5440013|5411298_5411601_-|WP_042215739.1|DBSCAN-SWA
MGRLLRLGDHVNHCYSNAEGEAVQDVLRKHFDTGDSVIVSFKGMDSVSSSFINSAFIELLEVYDFTFIKEHLGFADTTRTINDQIKRRFSFEANNKLIRS
>NZ_CP009285|5399383:5440013|5402216_5403080_-|WP_042215716.1|DBSCAN-SWA
MTTPSTVPYGTQVKEAAAYIQSKFGSYTPAIGLILGSGLGDLGDQIEDAVYLPYEEIPHFPRSTVEGHAGRFVIGKLEGKDVIIMQGRFHYYEGYEMRKVVLPVYVMAKLGVGTLVITNAGGGMNRAFKAGDLMLITDHLNMTGDNPLIGPNDPELGVRFPDMSRAYDPEYIALAKKLAGEVKGVDGEALVLQEGVYAGISGPTYETPAELKMLAYLGGDAVGMSTVPEVIVASHSKLRVLGITCITDMAIGDELEPLTHEQVVKVANLTKPKFIGLVRSFVREVQV
>NZ_CP009285|5399383:5440013|5429839_5430391_-|WP_042215775.1|DBSCAN-SWA
MSDINNIYAGPGIFTWGINADGTEESDAITIDLTQGGINFTTTTTYFEPTVDQTGTAPVKSIVTGTTGAINFETPDMDFEKVVSYNPNASKVIDGDTPAKVKYQVTGLAGKELPRKRAVIKPQGITDPSRFIYIESVGIKFDMNAAFVLDNNLRLTVAAMAYPDVNATPKGLLYTWGDITATA
>NZ_CP009285|5399383:5440013|5438261_5438714_-|WP_042215801.1|DBSCAN-SWA
MVNSIKKNKFQYELGEKWAREFFNGAEDHSFILETRAHDYERDHLGASTDVALTKKQIGDLLTKFEFLETKNNDLVIIRTYSKGGQFSPAYCFIVVANQQLLENNKKTPLYFRLSGKNGKEDWLVKGKGLVQYFPIDTSLLETGTGHENQ
>NZ_CP009285|5399383:5440013|5431600_5431918_-|WP_042215785.1|DBSCAN-SWA
MSLFGYPATVSHYHPGVDDWGRPLPAVPVEKDAKVVEEQKLVKNAKGEEITVAYTVYLEGINAVGFDDWLLYTDAIGTEIRIDVKHYEIRKYLGTDDVKEVVLYG
>NZ_CP009285|5399383:5440013|5415336_5415900_-|WP_042215751.1|DBSCAN-SWA
MKKKVFVIMTSALMLGGSIGFAAASSPLIGAKVQGLFTVQKADGTKIGDAVIINGSAYAPVREVAEAVGTNLTVEGKKIIMSDIQTIASDSTISNGTSTDKSDSREFIEYKIRAAESEIESAQGAIKGLEDSKEKVKMYPADYPTEQQKLDALAKIDEMIKAKQKIITFNEEELVRLKTLLDEPSTP
>NZ_CP009285|5399383:5440013|5434451_5435156_-|WP_042215792.1|DBSCAN-SWA
MYTYISRRFPRFHQFFAPDGGGGEGGAGAGGGEGGGTGGEGGAAGEGKTFTQAELDAAVQSRLSRAEKAAQKTLAKDLGYDSVEAMQAALKPKDKEKGDGKLDPAEVDRLVEDKIKAREKEQNDKTFKRLLNAEVKVLANELGFADWEDAAALSDLTAVKENDKGELEGVKEALEALAKKKPHLLKAKAGSTGRFGATVPNSPDQKKSALENIKKLAQNDSTATAAANDPWAKK
>NZ_CP009285|5399383:5440013|5407059_5407527_-|WP_042215726.1|DBSCAN-SWA
MEARIDKIKQQLQSQGYKLTPQREATLRVLLENEDDHLSAEDVFMLVKEKAPEIGLATVYRTLELLSELHVVEKINFGDGVARYDLRTDTAKHHHHHLICVQCGTMDEIREDWLGPLEERLEKDYNFTVLDHRLDFHGICYRCKDKNPAEGNTPE
>NZ_CP009285|5399383:5440013|5419376_5419733_-|WP_042215760.1|DBSCAN-SWA
MAKKWKTTEKVIKKFQEKYKDKAATTLGAVLKDVDPQKIIAINESYDYPSILNDYKMGILKESVEKNGWTNERPDGIYLIELPNGDLLVGGMGNHRAVLAKELGIPSIKASVGLVKFL
>NZ_CP009285|5399383:5440013|5418530_5418815_-|WP_042215758.1|DBSCAN-SWA
MKCEFCGKDHTESLSNGEPIEFREIPQGNGEFYWVCLDCFEVIEEYDEYEPMNIKPKWHLYSLKEAKRLWKIIKPAYDRETLERMLSDLDKTSE
>NZ_CP009285|5399383:5440013|5421328_5423737_-|WP_157764101.1|DBSCAN-SWA
MITKTLDLINLQRHNDNYADIQTDLTDHEGRITGAQSDITIHKASTTAHPAAHVTYSGAVAGAANIQEAIDFVDERLDTIIVGGSEDKDPELTDIKTPDPSYTPGRTIAAAGDVVRDMQKQFGEQLGDVAYGGQASLYGVEPTGADQTTELNTYFEALEDKGIRYAMFDKPGTFVPDSALSGTSKVLKIGNAEISRKNPVNWFTHISKTFRGFSGKINSSAVRGLTEAVDTGGFRRVAEAISQNQPVKVCIFGDSISTAGWDTANLKLRSVKGSSNPLGYINGPDASAESAAYPIKLMEMLVNSFPDTTFKYSNFSIGGEVINNWGVSRTIQIDNVWITKTWIDMCKDAAPDLLVIAFGMNHASNDSARIFSYYLKTLLDYVKANFTVIPDIVVITSPRCAYLPGETTWGTYTTHSSIHAAANAARAIGQEYGAYVCDVARITDIKRIGLDLTRPMLKKISVSDFNKILNGVTDNGDGTYSFINGASLSLAGNLQKDFQLKLKLNFHVLGSSTGHSLTVKFNKTNPGFYDNAVIFSPKSPSNLAKIDSAMRIADNAHYTIFITGSYADTVAYEGVDVVLTITKQGPIVEIKLGDNETRIIKDYADCWDVPGTLDMLYTTGTAGESLLVKSIEVWGAEYPEYLPVLLDREMFGAYAAGDYSVKQPYGGNGVNHPSSIGIEEGYVPALVELVEDIKHVVSIRNRNTDWSLFPVTETRDSIASGVTGISVIALGSITDYPKLTARVVSSGGTVYKLNRVYNASPYDHGVLLGTNEFGIYNDSGTVRLVIKSAATTGWVVTTHRRA
>NZ_CP009285|5399383:5440013|5399383_5400577_+|WP_042215712.1|transposase|DBSCAN-SWA
MTILPEMQLNNLFENLVTQFVKDNMESIMRAEMQAFMASEEAGTRNSRNGYYTRNLHTKYGNLEDLEVPRDRQGLFQTQMFEPYQRRDGWLEEAVIQMYKSGMGTRDVARFIESMFGSHYSPTTVSNITATVLEDIHQWQKRPLSKRYSVIYLDGLYVKLKRGTVRGEVVYFAMGIDEEGQRQILGFYVGGQESSNGWREVLKDLYNRGAQEVLLGVFDGLPGLDAAFKETYPQADVQHCVVHKVRATFPKIRIEHKTDVLEDLKTVYTAPDEVVARAHFDTVKAKWNKLYPKEMKSWEEQLSTLLTFYKYPEPIRKAIYTSNPIERMNKEIRKRLKPMNSLTNMDAAEKIVYLEMLDYNERHAQRVVPGFGMDNVKKKLNELFEARYPSLPTPEEE
>NZ_CP009285|5399383:5440013|5432311_5432671_-|WP_157764102.1|DBSCAN-SWA
MDIKLKGVVKNGGKWLKPGDIVRKVDDEIALDLIAKEYAEEVEPLPEDDTELQALRERAKVLGVPQAGRLGEAKLKEAIAEKEAELQELRTKAAKLDIEGFDTKTAEELTAAIAEAEKK
>NZ_CP009285|5399383:5440013|5435642_5436698_-|WP_042215797.1|DBSCAN-SWA
MATSEELIAQYVLTDERLRALVQSLEVGNISNRRRQQLLRQVEVIIEELTSSAGQGLADLVGSEYRNGAAIAVEQMTAAGIAAEAVNSSLKIIIHQQAAQTISDEGFYSILEASEHMSRDAKRRIETAVSRANEQSLIQGVSRRQATKNAVAEVNKQGITGMIAKNGAEIPADKYMAGVVQYHQRKAHVTGTENMAVQNGQDLVYVNSVGITCSMCAKYQGRVYSISGADKRFPKLELRPPYHSHCVHSLSVWVEEYTPAAEVEQTIKDSNRSFEQESRTEANIKRYNELQREKSRKNETRKQWIRYKATLPDDTPDLKQFASNKVRGTKKYGELQELYRAANIEIKKKGG
>NZ_CP009285|5399383:5440013|5412999_5413917_-|WP_042215741.1|DBSCAN-SWA
MIKNKYPIERRYINKRSNVRPGTRLVTGTPGFLVAHDTGNPGATADKHFEYFQTLVNRSASAQVFVDDKRILEIIPTGTGTDPAEKAWHVLYNVTTDNAKYGDDANDIALGVELCYGGKINTLEAYKRYVWYLAFCCDKWKLNPLTHIPSHKQLDPTRKSDVDQALATIGKTLKDLLYDIVKDMQEEPAVIVAPTALQLPASVAQALIEDYVSPAWFAARKAGDSVGTLHLHNLANNLRLAARIPLQPGSAAPFTQLPKSNVQELVFRWLSPGWQAAKVKSDKTAMAFYNNTANHLRRAACMPTE
>NZ_CP009285|5399383:5440013|5431155_5431608_-|WP_042215783.1|DBSCAN-SWA
MADNGAFSFELDGLDKIIDRLDDLEKDIEIRLDATLTKLAMKIIHDAKRLAPNDSGDLEGSLEVGELIQLIGLSSIDFGATVDVNDYSVIQHEGFNKSSLGKVITLKPGEKTLSKGNYRGYMPGKKYLANAIKLNEKLIKSELSKILEGW
>NZ_CP009285|5399383:5440013|5433854_5434436_-|WP_052429614.1|DBSCAN-SWA
MRLQPRPLFEVEGDYEIFASMEVVRFITNGATVDYTKVPADANGDRIIKKGTPMAKITASGKYRPYTGGLALTANVAANATTAVLNDVSRLVVGDIITFYNGTNTEPKTITAINAGTKTITFTAITNAYTTANGVLTNADGGDNPTFITVRTSNVKDGDHVIGGVEVAKLLSARLAVTVDAALKAKMPGITFA
>NZ_CP009285|5399383:5440013|5400885_5402217_-|WP_042215714.1|DBSCAN-SWA
MRAVDLIQKKRDGGELSREEIAFLIQGYSKGEIPDYQISAWAMAVYFRGMNARETGDLTLEMAMSGDQVDLSPIAGIKVDKHSTGGVGDKTTVVLAPLVAAAGVPVAKMSGRGLGHTGGTLDKLESITGFSVEMDRERFFTQVGEIGAAVIGQSGNITPADKKLYALRDVTATVESIPLIASSVMSKKIAAGANAIVLDVKTGSGAFMKTLDDSIALAQAMVDIGTHLGRNTVAVISDMDQPLGFGIGNALEIKEGIETLKGHGPKDLQEVCLILGSQMLVLGGKAKDEEEARSILLSHIEDGSALDKFKQMVTAQGGDVSQIESPDTLPAARKFIEVKAATAGYVESIQAEEIGVAAMLLGAGRETKESVIDLAVGIQLSLKVGDAVAAGDTLAVLHVNDASESKVQEAEAKVLEAYRISAQPVPPQPLVFALVTKDGVTRY
>NZ_CP009285|5399383:5440013|5420026_5420521_-|WP_042215763.1|DBSCAN-SWA
MNNDKVMENLVTNWGLPKCLERDKEHIIFKFDDEGITGTSERGYHCNVRDVKFCLYNERTDKVVFSMDFFKGSPSLPGRHMSRIVLELLYVHDESLRRKGVASYYFNRLREYALEEKVKCIYVRADANANNFKNDDRLNALNQTELEMFYKIKSTLEMPVYVES
>NZ_CP009285|5399383:5440013|5423773_5424568_-|WP_042215770.1|tail|DBSCAN-SWA
MNDVSVNGVWLSTLNILLVSRDLPPLPDTEENTIKLAGRDGVKSFGSTYAARPLGLGLFIMGDDYYGTVANLARVFDVKNGPAIVIFDDIPQKRFIAEYRGSMAFDTSTGNRKIDVPMKMDDSWIESIQDTELREYGEGLSFGEGYFYISDSSFSITASGQTFTVNNEGSTLAYPLIRITGAFTNLSMSDGIQTLTITGSAGTNDVFEIDCDLDKCSVRLNGVNAWSRSNGVFFVLEPGETTFTVTATSPNITVEVIYRYQYLY
>NZ_CP009285|5399383:5440013|5438750_5440013_-|WP_042215803.1|terminase|DBSCAN-SWA
MSAPVVVAFNSHFKIINRSKHRYRVMRGSAGSGKSVNIAQDFILKLGDPKYEGANLLCVRKVNETNRNSTYAELVGAINRIYGDQADEYWEVLRSPLMIRSRVTGNEIIFRGMNDVRDREKVKSITFTKGKLVWIWVEEATELQESDVDILDDRLRGVLLNPYLYYQITFSFNPVSASHWIKRKYFDYSSPDILTHHSTYLQNRFIDEAYHRRMMMRKEQDPDGYEVYGLGEWGELGGLIFKNFIVHDFDTSFGMFDSMHHAQDFGFNHANAILTVGVKDGEFFVCNEIYVHEMATDGIIELADRQGLSKYLAMYCDSAEPDRIQMWQNAGYNASGVMKEPGSVQAQIDYLKQRKIHIHPDCVNTIKEIQQWSWRKDKKTGLYLDEPVNVFDDAMAALRYSAEPLRRPESIYSNQRPSGW
>NZ_CP009285|5399383:5440013|5410737_5410938_-|WP_042215738.1|DBSCAN-SWA
MKMSIGQTIEMIYLDKAGKITQRKIEILGIRDGRIRATCLTTNAPRVFLVANVLSWRPLAENRHAG
>NZ_CP009285|5399383:5440013|5408669_5408915_-|WP_052429609.1|DBSCAN-SWA
MMLPVHLRLAEIFHINMTGPLTIEEAKELQYCLRENARYCWDCLMIQNQSVLAGATHDHEWQLELQRKLEVLRLTGRVPKV
>NZ_CP009285|5399383:5440013|5424564_5429049_-|WP_052429613.1|tail|DBSCAN-SWA
MAGGNLGELKARLTADANGIKRDIKEVKKDFASMGETAKKAGMDLQTLNRALAESGVSAEQISKINKSMGQAEKSTIGAADAAKKMGNHAHEATGSFMKLNMALQDVGASGQNIDNINAAIRRANPEVFEQQLASVREELENLGVSSSVIDDIIEQMQELNEVTGSVDFEIQSLGAAYAAMAIAVGAAIAKSVQTAADFEQAMQNVKAITEATGADFEALRINAIKLGAQTKFSASQAADAMSELGQAGFDTKEIIAAMPGVLSLAAAGNVDLATTADIASSILRGFGMAATETTRVVDVLASSSISTNADVTDLGMAMKYVAPVAKSMGLSLEEATAAVGALSDAGIKGEMAGTGLRAILLALASPSKEAAGYMDKLGFSIKDAAGNILPLSGIVQQLTEIWPRLTQAQQADVAATLAGREAASAFITLIESGSGKLNAYTDSLAEAGGTAERVAKTQMDTLKGAADNMGSAFESAGIIIGDMFLPAVREAVEGITALLTGFSELDKSTQAALITFAALPPLLLGGVVVAYQLKKAIDAVKIAYEAAILAGTLTARTIPMLGLLAVAIGAVAAGAAFLVGKYNESKEATKNFEAAQAELNDTLNDSPVKRSVDDLTELRKKTEDLTKALHEREKLQQRLNEIQKKADAGQGNPQMLSEAMDINEQLEKIDKNLRSMGFDGAEKATEKLKEMNTAIKGSVGALFEEQKAEVSDLAAKNDKLKALEKSLATFKKLSSAQKLDQAQKKELVDATNALKREYPGLNAVQEEDGRIRADNIGVIEGQIESDRYFTNQAISGASKRMQALVTETAAQKAAVEAQIKNYGELLKSMNAVNGVQASTFAESVKQNEERAKRTTPNVMDIVNNTLKVQTEKELTKLTDQQRELAEKQKVIEVAAAALSSGNFDLDGPNGPGIDLTDPEKPKKDKPATGKTAAELAAEARQAAYEADLKTIQFQADYYDLTAEKQMEKYEALRKKHAKFLAESVDDARTLTLQLKRLSEDSVKSRYDFSATWIDAESKRMEDSGKTELQIAQMKLDSWTRLRDRYSKDSEQYKAADDQVRQSRKEVATETETQISELYEKRSKLIEKEARRLEESGATEAEIAAYKVKAWTDLRNQYAIDTTYYEKADEELYQSRKDLTDKTLDLTKELVDAEKDRIDEAQKAELAAIESRKDAYVTAQDAKIKAIDDLLAKEAEANSDLDYEEELAKKNARIDLLASAVGKDGLKERQKTIEERDKLIEDHERDLRKRDLNNQKDALQDEKDVQLQAFEDEKDKTEAHYDDLKEAFDTYSDDIKVIEAGIAAFRVSSAGTANTQILTDLDAFIIQYQSKMSAISAAKQAAQKDADLAEYNANKDAYAAAAAAGNRTEMVRLASRNQALRDLYGITKDTGDKLQSFDVGGIIPGAAGAPVPIIAHGQEAIFNTAQLNGLFRILDNPSIIGAAAGVTKSETKVENHIDMSVNGVTLEDRADTEILYSEREKTARRMQTMGVKSG
>NZ_CP009285|5399383:5440013|5429052_5429319_-|WP_042215772.1|DBSCAN-SWA
MLDKTQHQIENEYFFIDLPQLLLLKDQARASEVIAQLEIASYPHITDQKVRQEIINRYIKVLPKAPEKPRASAEDQYQAQLARMKGGG
>NZ_CP009285|5399383:5440013|5420720_5421332_+|WP_042215765.1|DBSCAN-SWA
MSNITKTLKSTRLFVKNFNSRIKLKNDNFSIISNNCWGGQVYKNLGKPYNTPFVGLFIYGPCYIKLLENLDYYLHTPLTFTDTSQYKETPSYPVGLLHDIEIHFMHYTDENEAYEKWNRRLARFNWNNIFIKLSDRDLTSEEHVQRFDALTYPKVFFSSKNTPGINSLVWFREFENSSTVDNEMLVYKKYFNAVNWLNTGKIS
>NZ_CP009285|5399383:5440013|5406653_5406887_-|WP_042215724.1|DBSCAN-SWA
MIVSIPKTVRRLYFMTLLVAISCVLYYILSWFSAWMSPAQNYDIPEGTAIRAFHDVKQGDEGLSAGQRLRLYYWYGE
>NZ_CP009285|5399383:5440013|5413913_5414291_-|WP_042215742.1|DBSCAN-SWA
MRANDTITLICYALSLICIIYITAAMHIYFRKKYREGVVGIGLVLGMLMFTAYALERLVGFVIRFGKVQGWTGYYFDLLQKWGWTIGVIGTTVTLCALAILVQGRDLGLFLERPSGKRKGGSGRR
>NZ_CP009285|5399383:5440013|5435403_5435637_-|WP_042215794.1|DBSCAN-SWA
MDEIKERRDLRAGKVTPLACAGSLQQAAEQGRIEAFVAVVKLADGSIQTVWSHIQNTEALGLLECGKDDVMIQMREG
>NZ_CP009285|5399383:5440013|5429351_5429759_-|WP_099052487.1|DBSCAN-SWA
MFPLTRKDKLKLGSRTVSIPKLTRNRLKKLTDHLGTIGDLLVKIFLTPEADRSVMIVAGAEIMIDEIYELTSLMSDIDINELSEQASLAECTEYLNLTWQKNDMNTALKNLSGLIPPMAQQFVTSIAARQSQAQG
>NZ_CP009285|5399383:5440013|5409041_5409263_+|WP_042215731.1|DBSCAN-SWA
MIKNNVKDIMDRQNKGIRGTARETGLAINTVSGLYHNTSKRVDFETLEKLCKHLKVSTGELIEYIEDKEAQPE
>NZ_CP009285|5399383:5440013|5403131_5403956_-|WP_042215719.1|DBSCAN-SWA
MTAVTQSNIQEAAVYIKDKCTVAPEIGLILGSGLGVLADLITDEVVIPYNEIPHFPVSTVEGHEGELLIGMIEGRRVVMMKGRFHMYEGYGPETTAFPVRVMKELGVTSLLVTNAAGGVNTEFTPGDLMLITDHLNLTGRNPLTGPNDNALGVRFPDMSSAYSPRLIAAAKEAAAALNFEFKEGVYAGLLGPNYETPAEIVMLRRQGADAVGMSTVSETIVARHAGIEVLGISCITNMAAGILEQPLNHAEVMETAERVREQFLKLVLAFIPKM
>NZ_CP009285|5399383:5440013|5432733_5433819_-|WP_042215790.1|capsid|DBSCAN-SWA
MDPELLLLEEALSGEELLVYASNLTIQNDYWQNILFPPLQTDELTVDVIKSASSLPVMAQIAHLGTETKYGSREGTSGQRIEIPKIQRGRWMDEKLIRLLLMASQASGLRRQEVASIVRDQLDDAKYAVSSIRARKEWIAMQAASLGAVNYVEDDVRITVDYGFTNDQKPVLSGTDRWSDLVNSTPLLDMQTWYNIQKARGVILERAFTSQTVLSYLLNNLSMRQFYFGNPTGTAVPPQLDSSQLDQITDRMKLPRILAYDTVARTEDTALVNGKTSYSTVRMTPEDRFVMLPGGKLGDYLWAETTESMVSGIEAETTAENGIYVFRDLVSKHPLRLRTVGVNLAFPSFPYADSVMSATVI
>NZ_CP009285|5399383:5440013|5415967_5418022_-|WP_042215754.1|tail|DBSCAN-SWA
MQKHLKSFDRNRTPTGLLVATTDVQRRRRLNSDYEISFTVPMTSTDYKELIIPKGHVQDERGQFYVVQSRARDRSNKVISAQIICTHIMFKMIDSKMPYDDYIDEAYGVHISVLLDKISTATGGIYTFVTHDTFDLRDVKDWGATTALAALQDTVNLYGCEIDPDNFVIHLYKRIGSDDGFEYRIRKNIINDSFKDNVSNLTTRLFSQMKDGRTFIGLSADYLTTEERSLLQSVPGAIVDNKLAVNYLISPYTQYWTNNVNAFYDGELIDQNIEDPEELLIATREALRKKEMPEFEIGVSAADIYKIDPDEQRPGLGDTVYAYDPEMELQRVSCRVMELTEYPFSMDKHSQATLSNYQMRDDTQVLADLERSKQILNDLLSGGRVRAAAFEEFAKQAVIDINASKSEIIYDSRGIVLQEVDHPNVQMVLTSHGLIITEDGGATARTAITGRGIAAEVIAGVLGSFVSMEIGSGNNITKINPSGISAGHADFNSAPFRVDMAGNVVARSITLTGLIEESTMTYSDIIAGTVTGALIRTAAAGARFEVDETGWRTYDASGTRRIGIYQDAGYNMSALTFDQSNGTRSGVINGGDGLFEVRSAGDNDLFLSAMTNTIFFQGQMNFASAYSVSGFGINFVSGLRAELDSIWSALAGKASASHSHTVNLGTHNHGIAGAVNWGGSFTVS
>NZ_CP009285|5399383:5440013|5436699_5438199_-|WP_042215799.1|DBSCAN-SWA
MTIIYSKKRFPPPPYDVEVEDMNYYRLLYGGDHDQIFPRARSIQTTERVFRRSRPGLIRRGMSADIKITSEHQYVVVNFASLVAEVPADLINRALGNVSADVEAGPELEFVSAVVTASKPNDKIWSAITQHQVDGLIAYRIRRSAKGKVWFEWVLGDRFFPHEDGSGADLAWIEEWDDRRGSKLKFLRVERQELSDEGLTIQQQVYEMDGETVGDQIDINQYAVTYEIEIPDDETLKDVTELLCGFVINDETLLHPRGRSALRNIDTIQEEINWTITRDSIVFDKHGKPKLAIPRALWDTVANQNQRDYGARFVRGADLEVVSFDEKTGAIPQYITWDAKTDQSFKHVERLIRYLLAVSKTSVQAAGLEDAKGDTGIALLYLWIQSVIKAEAIQAKFDGAIKDAIRKCMLLENAIGKGGLKPVNPVIEWGTMLPKAESEKDEEESKKYVDGVQSLETTVRRMHPDWSEEAIAAEIQKIQDEKAVDTLNPTYTQPPRVTV
>NZ_CP009285|5399383:5440013|5430749_5431151_-|WP_042215780.1|DBSCAN-SWA
MLASDLINFLTGAGYSVYPDANFVPADLPEAKFPCLFVEDSGGPPPDDYVPTERPSYQIIVKGKSYKANPVNMATAEAVAKGLSKLLHRESNYMVGSTYVFSSVATMQPSFIGLDEKDRPIYSTNFEFYAREE
>NZ_CP009285|5399383:5440013|5410439_5410748_-|WP_052429610.1|DBSCAN-SWA
MLDDTARKLLRVMFQFHGHFRRMPSLPELERLSGRRSAAIKAGMLQLVEQYYIQWDDKQPVETAVVIEAWERDVPFKDHVAAGPHKSQQAEITGNIDYWTEY
>NZ_CP009285|5399383:5440013|5411585_5412485_-|WP_052429611.1|DBSCAN-SWA
MDALRVYLPKEFDKDNMYYFINEVFDENMDLRARDYVFDFTPLRFIRPVGVTVLSNIIGRLKKQGAHLSITYFEPDRSNRRCPMAFLDDAMFFKKFIDRTLDEKSSLRMTTLPLEHVEYNRSYEYLDYAMSWLAGKLNLTKESLGDIKSCLVEVFNNIIDHSAEHTGSIFVQHYPRESRVMVAISDFGVGIPSSIQDILPGVDDAEALLLAIKEGFTTKSTPKNRGAGLDFLLQNVVINNKGSVYIHSNHGILSSTSGRDGMEITSRKTEGFYPGTLLEIVFQTDTIEYVEEEFSWDVY
>NZ_CP009285|5399383:5440013|5412625_5412988_-|WP_052429612.1|DBSCAN-SWA
MQTVIDQAQPYITAVVLAIVGILATVILRTIALLQVKADSFFDARLSVSQRELLHKIASEGFAYAQTVYKELGGEDKLQQALVYASDQLEARGIKAAPEEIRAAIEKAYLAYKATVLTKQ
>NZ_CP009285|5399383:5440013|5418126_5418498_+|WP_042215756.1|DBSCAN-SWA
MKEISKAKRAIEEIKNLEKYYKSQLTIEEISYLKFHFDKETEVLKQPFINVAAISFGAFVVGLMITQAFKENFLSAVFILSVIFLVYLGIMGSMHYSKLKYYTIRKHITEKILNEVEQKEPLE
>NZ_CP009285|5399383:5440013|5405614_5406508_-|WP_042215722.1|DBSCAN-SWA
MESHLQPFMQYLSGDKGLSPSTLESYGRDISQFLEFTEERGTAAMEEIRRSHIMLYLGALRGAGKATATVNRNTVSLRAYFHFLLKERLIGQDPTLDMETIKPSKKPPMILSIEEIERLLAVPDESAPQGMRDKAMLELLYATGIRVTELISLNVEDVNTGLKFARCSGASGKERVVPIGTIAADCVARYVSGMRDKLLRVNQEEPALFLNSLGGRLTRQGFWKIIKKHAREARIQQDITPHTLRHSFAAHLLEGGADLRSVQQMLGHSDISTTQIYSGIARKNMKEVYENHHPRAK
>NZ_CP009285|5399383:5440013|5410101_5410428_-|WP_042215736.1|DBSCAN-SWA
MGKKLESVWEGSRFLLPEHVQLLRQEMQEQGRRSRPAIDPDEWELIDQALGYALLEKEQITIVLFDPYKDLKVRGVVVKVDRQLRRIKFQMEEDFSWIKIDDVIRVIT
>NZ_CP009285|5399383:5440013|5431914_5432301_-|WP_042215786.1|DBSCAN-SWA
MPTTEEVNLWIAENVLDTEAWDKKPLKQPLAVKQAERNLARWYPAVILTVEIAALQSIWEMQGLDPALKFQKHGVKSVDDHGEGVTYSGIRDVVAPDVRDLLGKTASEIAEEEAEEGGTDLQYGGCLI
>NZ_CP009285|5399383:5440013|5414497_5414782_-|WP_042215747.1|DBSCAN-SWA
MDLPSLKDALSLADQYGIGWLFALGEALLLVIVGRWLVIGKLVPGKSLEKAEKQRDDAIEKAISAVAALNRSSDVMEKMKPADRLNPGDQDGGG
>NZ_CP009285|5399383:5440013|5409367_5410069_+|WP_042215733.1|DBSCAN-SWA
MNKPIYTKWWFWVLAVIIIGAIGNMGDDKNTTDQAVTSATIEPAKVVVAEATEEAVIVPTQKPKEVSKSDPTVAPTENPIPGTIGMTPEEFRKEFNARADSMESKLKISKKLTVEDGLAQDTFQYMFNDFLGITGSVNKADGSIRDIMMIGRGDGTSASGANIIVVMGLVILAVNPDIESTEVGSIITDLKVLEDGVDLAKIDESTVRNGIRYHVQGSNELGLMFSAGDANDK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042215712.1|5399383_5400577_+|transposase	IS256 family transposase	A0A0K2CZ57	Paenibacillus_phage	3.0e-33	27.4
WP_042215714.1|5400885_5402217_-	pyrimidine-nucleoside phosphorylase	A0A0H3UZD4	Geobacillus_virus	1.2e-128	55.5
WP_042215716.1|5402216_5403080_-	purine-nucleoside phosphorylase	Q5YBA4	Grouper_iridovirus	3.4e-55	38.8
WP_042215719.1|5403131_5403956_-	purine-nucleoside phosphorylase	Q5YBA4	Grouper_iridovirus	8.8e-53	40.8
WP_042215720.1|5404237_5405416_-	phosphopentomutase	NA	NA	NA	NA
WP_042215722.1|5405614_5406508_-	site-specific tyrosine recombinase XerD	A0A0K2CP59	Brevibacillus_phage	6.0e-39	32.9
WP_042215724.1|5406653_5406887_-	DUF4227 family protein	NA	NA	NA	NA
WP_042215726.1|5407059_5407527_-	transcriptional repressor	NA	NA	NA	NA
WP_042215728.1|5407869_5408310_+	hypothetical protein	NA	NA	NA	NA
WP_052429609.1|5408669_5408915_-	hypothetical protein	NA	NA	NA	NA
WP_042215731.1|5409041_5409263_+	helix-turn-helix transcriptional regulator	A0A0E3U244	Fusobacterium_phage	2.3e-08	41.1
WP_042215733.1|5409367_5410069_+	hypothetical protein	A0A2H4J8P0	uncultured_Caudovirales_phage	5.1e-09	27.8
WP_042215736.1|5410101_5410428_-	YolD-like family protein	NA	NA	NA	NA
WP_052429610.1|5410439_5410748_-	hypothetical protein	NA	NA	NA	NA
WP_042215738.1|5410737_5410938_-	hypothetical protein	A0A2I7SCV7	Paenibacillus_phage	4.6e-08	44.6
WP_042215739.1|5411298_5411601_-	STAS-like domain-containing protein	J7KJ12	Streptococcus_phage	2.5e-13	47.7
WP_052429611.1|5411585_5412485_-	sensor histidine kinase	J7KDG8	Streptococcus_phage	1.4e-27	32.0
WP_052429612.1|5412625_5412988_-	hypothetical protein	D0R7H9	Paenibacillus_phage	3.0e-21	48.0
WP_042215741.1|5412999_5413917_-	N-acetylmuramoyl-L-alanine amidase	A0A0K2CPP8	Brevibacillus_phage	2.7e-42	50.3
WP_042215742.1|5413913_5414291_-	hypothetical protein	NA	NA	NA	NA
WP_042215744.1|5414280_5414496_-	hypothetical protein	NA	NA	NA	NA
WP_042215747.1|5414497_5414782_-	hypothetical protein	NA	NA	NA	NA
WP_042215749.1|5414868_5415159_-	hypothetical protein	NA	NA	NA	NA
WP_042215751.1|5415336_5415900_-	hypothetical protein	NA	NA	NA	NA
WP_042215754.1|5415967_5418022_-|tail	phage tail protein	A0A0U4JID8	Exiguobacterium_phage	6.9e-22	23.7
WP_042215756.1|5418126_5418498_+	hypothetical protein	NA	NA	NA	NA
WP_042215758.1|5418530_5418815_-	hypothetical protein	NA	NA	NA	NA
WP_042215760.1|5419376_5419733_-	hypothetical protein	NA	NA	NA	NA
WP_042215763.1|5420026_5420521_-	hypothetical protein	NA	NA	NA	NA
WP_042215765.1|5420720_5421332_+	DUF1919 domain-containing protein	NA	NA	NA	NA
WP_157764101.1|5421328_5423737_-	hypothetical protein	NA	NA	NA	NA
WP_042215770.1|5423773_5424568_-|tail	phage tail family protein	NA	NA	NA	NA
WP_052429613.1|5424564_5429049_-|tail	phage tail tape measure protein	A0A1Q1PVX7	Staphylococcus_phage	1.4e-35	28.9
WP_042215772.1|5429052_5429319_-	hypothetical protein	NA	NA	NA	NA
WP_099052487.1|5429351_5429759_-	hypothetical protein	NA	NA	NA	NA
WP_042215775.1|5429839_5430391_-	hypothetical protein	NA	NA	NA	NA
WP_042215778.1|5430411_5430747_-	hypothetical protein	NA	NA	NA	NA
WP_042215780.1|5430749_5431151_-	hypothetical protein	NA	NA	NA	NA
WP_042215783.1|5431155_5431608_-	HK97 gp10 family phage protein	A0A1U9WQQ7	Geobacillus_phage	8.1e-08	29.2
WP_042215785.1|5431600_5431918_-	hypothetical protein	NA	NA	NA	NA
WP_042215786.1|5431914_5432301_-	hypothetical protein	NA	NA	NA	NA
WP_157764102.1|5432311_5432671_-	hypothetical protein	NA	NA	NA	NA
WP_042215790.1|5432733_5433819_-|capsid	major capsid protein	NA	NA	NA	NA
WP_052429614.1|5433854_5434436_-	hypothetical protein	NA	NA	NA	NA
WP_042215792.1|5434451_5435156_-	hypothetical protein	NA	NA	NA	NA
WP_042215794.1|5435403_5435637_-	hypothetical protein	NA	NA	NA	NA
WP_042215797.1|5435642_5436698_-	hypothetical protein	NA	NA	NA	NA
WP_042215799.1|5436699_5438199_-	hypothetical protein	M4ZRM8	Bacillus_phage	4.7e-44	27.8
WP_042215801.1|5438261_5438714_-	hypothetical protein	NA	NA	NA	NA
WP_042215803.1|5438750_5440013_-|terminase	PBSX family phage terminase large subunit	A0A0A8WJS9	Clostridium_phage	1.4e-174	70.9

Sequences of DBSCAN-SWA_7

Nucleotide sequences of DBSCAN-SWA_7

>NZ_CP009285|6566809:6571669|DBSCAN-SWA
GCTACTTCCGGTACTCGCCGCTAAGAATTTGCTCCCACCACTCAGCATTCTCCGTATACCACTGAATCGTCTGAGCAATTCCTGTCTCAAAAGTATAGGTGGGCTTCCAACCAAGCCGCTCCAGCTTAGTGGGATCAATAGCATAACGTTTATCATGCCCCAGCCGGTCTGCAACAAATTCGATCAATTCCTCAGATTTCCCTAAGGTATGAATAATAGTCTTCACTACTTCGAGATTCGTACGTTCATTATGGCCGCCTACATTGTATACTTCACCGCTTACACCTTCGTGCAATACGAGATCAATAGCAGCACAATGATCCCAGACATGCAGCCAATCCCGGATATTGGCACCATCCCCGTAGACAGGAAGCTTCTGTTCATTCAAGACCTTCGAGATCGTAAGCGGGATCAGCTTCTCAGGGAAATGATAAGGGCCGTAATTGTTAGAGCAGCGTGTAATGTTCATTGGCAGGCCAAAGGTTTCATGGTACGCGCGAACTAACAAATCAGACGACGCCTTGCTGGCGCTATAAGGACTATTAGGTTGCAGCGGTGTCTCCTCTGTGAAGAATACCGTAGGATCGAAATCCAGTTCGCCATACACTTCATCCGTGGACACATGAACAAATTTCGCCACACCAATGGTCCGTGAAGCATCCAACAGCACTTGAGTTCCCATTACATTCGTCCGGACAAATATAGCCGGATCTGTAATCGAGCGGTCCACATGACTCTCTGCTGCGAAATGTACCACATAGTCGAAGCGTTCTTGTTCAAAAAGCGACATAATCGCATCACGGTCAGCAATATCCGCCTGAATGAAATGATAGTTATCTCTATCTTCAATCTGCTTGTGCTTGGTTAAATCACCGGCATAGGTTAACAGATCCAGATTATAGACATCATAATCAGAGTATTTATCCACTATATATTGCACAAAGTTCCCGCCAATGAAACCGGCACCTCCGGTAATCAGCAATTTCTTCCGACTCATGAATTACACCTCAGAATGATTCGATTTAGTGTCTATATGCTTCAGTTATTATAGGTAAAGTTCAGAACAGCATCTTTCAACACAGGAGCCTTCTCGTCTTTGCCGGATAGAACTGGAGTAACATGTAATGGCCACTCTATTCCAATGGCAGGATCATTCCAGAGAATACCGCCATCACAATCCGGAGCATACAGCTCATCACATTTATACTGAACTTCAACGTCCTCGGTCAGCGTCATGAACCCATGGGCGAACCCTTTGGGAATCAACAGCTGCTTCTTATTCTCGGCACTCAGTTCAATTCCAAACCACTTGCTGTACGTGGGACTGCCTTGTCTGACATCCACTGCCACATCGAATATGACTCCACGCGTGCAACGGACAAGCTTCGTCTGAGCTTTAGGATTGAGCTGATAATGTAATCCCCGCAAGGTCCCTTTTGTAGCTGAATACGACTGATTATCCTGTACAAAAGCTATATCGATGCCCTGCTCTCTAAATTTCGCATCACTGAACGTCTCCATAAACCATCCCCGGTGATCACCGAACACCGCAGGTTCCACGATAAATACGCCAGGGAGCGCCGTTTCCGTTAATTTCATATCCTCCACACCTTTACTGCTTAATATTGAATCTTCCCGGTAGCTACCTTGATCAGATATTGGCCGTAGCCCGTCTTGCTTAGCTTCTGCCCGCAGCTTAACAGGTGTTCTTTCGTAATCCACCCATTAATATATGCAATCTCTTCAAGAGCGGCAATCTTAATCCCTTGATGGTCCTCAATCGTCCGGACAAAGTTCGTAGCATCCACCAGACTCTGATGAGTACCGGTATCCAGCCATGTGAAGCCTCGTCCCAGTAGTTCAACATCCAGCTCGCCCATTTTAAGATAGGCTTCATTAATGGAAGTAATCTCAAGTTCGCCTCTGGAGGAAGGCTGTACATTCTTAGCGATCTCTACAACACGGTTATCGTAGAAATAAAGACCTGTAATCGCATAATTAGACTTAGGCTGTGCCGGCTTCTCTTCCACGCTTAACACTTTGCCTTCATCGTTAAATTCAACCACACCGAAACGCTCGGGATCTTGTACGTGATAACCGAACACAGTCGCACCTTGTGCTTTGTCCGAAGCACGCTGAAGCATTTTACGGATTCCATTCCCGTAGTAAATATTATCTCCAAGAATCATAGCCACAGAGTCATCCCCAATAAACGCTTCCCCCAAAATAAAAGCCTGAGCTAGACCGTCAGGACTTGGTTGAACTATGTATTGCAGGGAAATACCGAACTGAGACCCGTCGCCAAATAGACTTTGGAATCTCGGAGTATCTTCAGGCGTGGAGATGATAAGGATCTCATTAATTCCGGCGAGCATTAGAGTAGATAACGGATAGTAGATCATTGGCTTGTCGTAAACGGGTAGAAGTTGTTTACTGGTTACCATGGTTAATGGGTAGAGGCGGGTTCCGGAGCCGCCGGCTAGGATTATGCCTTTCATATATATTCACCTCCAAATGTATTTTAGTGATAAAAAAACAACTTCTCTCCATCTTGAATTACTCGTTACAAACGAGAGTCTCAAATATTAGAGAGAAGTATATCTGACATATCGCAAATCTTATAAAAAATTCACGAAGATAAATCTTCTGCATTTCGAACAAGAATATTTTCAATAAACTCTCTAACTGCTCCGTCTCCACCATTAAACCTACTTGCGAAATTCACTAATTTTTTTATAGTATCCATCGCATCTGCTGGACACCCACTATAGCCACACAATTTCATGCATTCTAAATCATTTTCATCGTCTCCAATATAAGCTATATCATTAAATGCCAACTCGTATTTATCACTTATCATCTTCAAACCCGAAATCTTATCATGTATACCTTGGTATACATCAACTATATTTAATTCTCTAGCTCTATTGGCTACAATTTCTGAACTTCGAGCAGTTAATATAACGGGTTTAATCCCAATGGCATTTAATTTAGTAATTCCCAATCCATCTTTTACATTAAAAGCCTTCATTAATTCACCCTGTGGTCCAATGTAAATCTTCCCATCAGTTAATGTCCCATCTACATCCATTATAAGCATTTTTATCATATGATTATTCCTTTGTTCAAAATTGCTTGTATTCTAATGGTTCCTACTGCTTTGTTTTGCTTATCAACTACGGGTGCACATGATATGTTTTTTTCTTTTAGTATTTGAAGTGCTTCAACTGCCATACAATCATGCTTAACGGTGACAGGCGTTTTTGTCATGATCTCATCTACTGTTAGACCATAGACATCAACACCTTTTTCAAGTTGTCGTCTTAGATCTCCATCGGTTACAACACCAATAATATTAGCCTCATTATCGACTACGGTAACTATTCCAAGACCTTTTTTACCCATTTCAATAATTGCACTTTTTAAAGTAACATCTTGTTGTATCATTGCATTATCTTCTCCATACGCCATTACATCTTGAACTTTAATCAATAACTTTTTACCTAATGAACCTGCAGGATGAAATAATGCAAATTTCGTTTCAGTAAATCCATATACCTTTGACGCTACAACAGCTAAAGCATCTCCGTAAACTAAAGCAGCTGTCGTGCTTGAAGTTGGAGCTAAATTCAGGTAACAAGCCTCCTCAAAATTTGGAAATACCTGTGAATAGTCACTATACTTCACTAATGTAGAATCAGCATTACCTGAGATTCCTATCAAGGTTGCACCAATTGCCTTAATATTAGCCAGCACTCTAGTAATCTCTTCGCTTTCACCGCTATAGCTTAAAGCAATTACGACGTCATCATTAGTGACCATTCCCAAATCCCCATGAAGAGCTTCTCCAGGATGTAAATAGAATGCCGGTCCCCCAAGACTTGCCATTGTTGCAGCAATCTTACGTGCAATATGCCCCATCTTACCCATACCAGTGACTACCACTTTCCCTCTGCATTCTGTTACAATTCTTAAAATATTGCTAAAATCGTCATTTAAATGATCTCTTACAAGCTCAAGTGCTCTAATTTCTATATCAAAGACTCTTTTGGCTTGATCTACATAGTCCATGCTTCTAGCCCCTATTCTATTAATTCACAGCATGATATACCTTTATTAATTTTTCTAAGATTGATTTTAAGTCACTTAACTTAACCATATTAGGACCATCAGATTTTGCATTATCTGGATCAGGATGAACTTCCATAAACAGCGCATCTATTCCTACGGCCATTGCAGCTCTAGCTAGATATTGGACATGGTCTCTATTACCACCAGTTGCATCCCCTTTTCCACCTGGCTTTTGTACACTATGAGTAGCATCAAACACAACTGGATATCCAAATTTCTTCAACTCTACTAAACCGGTCATGTCAACAACTAGAGTGTTATACCCAAACGTAGTACCACGTTCGCAGAGCATAATATTTGTATTTCCACCTTCTTCTAATTTCCGAACAACATTTTTCATATCCCAAGGTGCAAGAAATTGTGCCTTTTTAACATTAATGATTTTCCCAGTTCTCGCTGCAGCAACCAGTAAATCTGTCTGTCTACACAAAAAAGCTGGAATTTGAATTATATCAGCAACTTTTGAAACAGGCCCAGCTTGGTATGGTTCATGAATATCAGTTGCAATCTTTAAATTATACGTATCCTTTACCTTTTGTAAAATCCTAAGACCTTCCTCAAGCCCTGGTCCTCTAAAAGAATCAATTGAAGTTCTATTAGCCTTATCAAATGAAGCTTTAAAATAATAATCAATTCCTAGTTCGTCTGTTATTTCTTTTACCTCTTTCGCAATCTGTAATACTAATTCCTCACTCTCAATTACACAAGGTCCAGCTATTAATTTAAACAT

Protein sequences of DBSCAN-SWA_7

>NZ_CP009285|6566809:6571669|6569913_6570879_-|WP_042217108.1|DBSCAN-SWA
MDYVDQAKRVFDIEIRALELVRDHLNDDFSNILRIVTECRGKVVVTGMGKMGHIARKIAATMASLGGPAFYLHPGEALHGDLGMVTNDDVVIALSYSGESEEITRVLANIKAIGATLIGISGNADSTLVKYSDYSQVFPNFEEACYLNLAPTSSTTAALVYGDALAVVASKVYGFTETKFALFHPAGSLGKKLLIKVQDVMAYGEDNAMIQQDVTLKSAIIEMGKKGLGIVTVVDNEANIIGVVTDGDLRRQLEKGVDVYGLTVDEIMTKTPVTVKHDCMAVEALQILKEKNISCAPVVDKQNKAVGTIRIQAILNKGIII
>NZ_CP009285|6566809:6571669|6569437_6569917_-|WP_042217107.1|DBSCAN-SWA
MIKMLIMDVDGTLTDGKIYIGPQGELMKAFNVKDGLGITKLNAIGIKPVILTARSSEIVANRARELNIVDVYQGIHDKISGLKMISDKYELAFNDIAYIGDDENDLECMKLCGYSGCPADAMDTIKKLVNFASRFNGGDGAVREFIENILVRNAEDLSS
>NZ_CP009285|6566809:6571669|6570898_6571669_-|WP_052429663.1|DBSCAN-SWA
MFKLIAGPCVIESEELVLQIAKEVKEITDELGIDYYFKASFDKANRTSIDSFRGPGLEEGLRILQKVKDTYNLKIATDIHEPYQAGPVSKVADIIQIPAFLCRQTDLLVAAARTGKIINVKKAQFLAPWDMKNVVRKLEEGGNTNIMLCERGTTFGYNTLVVDMTGLVELKKFGYPVVFDATHSVQKPGGKGDATGGNRDHVQYLARAAMAVGIDALFMEVHPDPDNAKSDGPNMVKLSDLKSILEKLIKVYHAVN
>NZ_CP009285|6566809:6571669|6568427_6569306_-|WP_042217106.1|DBSCAN-SWA
MKGIILAGGSGTRLYPLTMVTSKQLLPVYDKPMIYYPLSTLMLAGINEILIISTPEDTPRFQSLFGDGSQFGISLQYIVQPSPDGLAQAFILGEAFIGDDSVAMILGDNIYYGNGIRKMLQRASDKAQGATVFGYHVQDPERFGVVEFNDEGKVLSVEEKPAQPKSNYAITGLYFYDNRVVEIAKNVQPSSRGELEITSINEAYLKMGELDVELLGRGFTWLDTGTHQSLVDATNFVRTIEDHQGIKIAALEEIAYINGWITKEHLLSCGQKLSKTGYGQYLIKVATGKIQY
>NZ_CP009285|6566809:6571669|6567846_6568407_-|WP_042217105.1|DBSCAN-SWA
MKLTETALPGVFIVEPAVFGDHRGWFMETFSDAKFREQGIDIAFVQDNQSYSATKGTLRGLHYQLNPKAQTKLVRCTRGVIFDVAVDVRQGSPTYSKWFGIELSAENKKQLLIPKGFAHGFMTLTEDVEVQYKCDELYAPDCDGGILWNDPAIGIEWPLHVTPVLSGKDEKAPVLKDAVLNFTYNN
>NZ_CP009285|6566809:6571669|6566809_6567805_-|WP_042217104.1|DBSCAN-SWA
MSRKKLLITGGAGFIGGNFVQYIVDKYSDYDVYNLDLLTYAGDLTKHKQIEDRDNYHFIQADIADRDAIMSLFEQERFDYVVHFAAESHVDRSITDPAIFVRTNVMGTQVLLDASRTIGVAKFVHVSTDEVYGELDFDPTVFFTEETPLQPNSPYSASKASSDLLVRAYHETFGLPMNITRCSNNYGPYHFPEKLIPLTISKVLNEQKLPVYGDGANIRDWLHVWDHCAAIDLVLHEGVSGEVYNVGGHNERTNLEVVKTIIHTLGKSEELIEFVADRLGHDKRYAIDPTKLERLGWKPTYTFETGIAQTIQWYTENAEWWEQILSGEYRK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042217104.1|6566809_6567805_-	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	3.9e-79	46.1
WP_042217105.1|6567846_6568407_-	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	5.3e-41	44.2
WP_042217106.1|6568427_6569306_-	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	3.0e-107	66.3
WP_042217107.1|6569437_6569917_-	HAD-IIIA family hydrolase	E3T535	Cafeteria_roenbergensis_virus	6.8e-21	35.4
WP_042217108.1|6569913_6570879_-	KpsF/GutQ family sugar-phosphate isomerase	A0A2P0VNK5	Tetraselmis_virus	7.2e-38	35.4
WP_052429663.1|6570898_6571669_-	3-deoxy-8-phosphooctulonate synthase	E3T537	Cafeteria_roenbergensis_virus	3.8e-58	48.2

Sequences of DBSCAN-SWA_8

Nucleotide sequences of DBSCAN-SWA_8

>NZ_CP009285|7334467:7387354|DBSCAN-SWA
TTCATCGGTTGTTGAAAGCCAATTCAAATAATCCTGTAGCAGACAATCCGGCAAGTCCACCTGCCCAGAGACGTAGGGTAATATCGAGGTCAGTAAAAGGATACGCTGCAGCTCCAACCAGCAGTCCAATTCCTAGTCCTACAAACGGGATAACGTTGCGCGAAAGACGGGTGTTATTTTTGATAAGCTGCACCAACGCCAAAATTACTACGGCCAGAATTGAGGCAAAGGCTAACACATTATCAAACAGTTCACTGTTAATCATGAGCCCGCCCCCTTCAGCCCGCTGCTTATGATATCCACTGTTTTTGTTGCCGAATTATAGCCGACCTGTGCCCCCAATGCTTCGGCAATAACGCGAACGGGAGCATAAGTAATGCCATTTACCATCATTCCTTCTGCAATCTTCACACCGTTCACTTTTACCGCTGCTGTAATTTCACTTTTCACAGTTTGTTCCTCCTTAAGCTTGATACGTTCATATACCGCCTCTACTGCCGCAGCAGCAGGCTTCTTCCCTGTCCGGAGTGCAGCCAGCGTCAATCCGAAGCTCAGCTGAAAATGCGGGTAATCCTTGAAGCTGGTCCAGTCCCCGCCCCATTCGAATCCGATCGCCTTGGCCTGCTGCACCACTTCCAGCCAATCAGCGGTACAGTCACTGTCCCCATCCCTGTTCATATCCCAGGAAACACTTGAACCATTCGGAAGCAGCAGCGCAAAATCCACCGCCAGTCCATAATTGTGATAGCTGTATCCGCCGCGTGCATTAGTGACAATCGCTCCCGGCTTGGTTCGCCCCTGAGCGTAGAGTGCATCCTGTTCGGCGATCGTCCGCAGTCCTTGAGTAATCAGGATGGGAACACCGCAAGCATAACAGCGTTCAATCAGCGTTGTGGCTGCGGCGAGTACTGCGGGATGAAGCCCGGAGAGACGGGCAGCGGATTTATTTAGAACCTGAATTAGAGTCAGCATGCGGATTCCTCCCTTTCCTGATCCCGGACAGCACCACGAACAGATCCTGCCGTTTGGTATACATTAACAGGGTGAGGATGACCAGCCCTAATGTGGTACCCGTCTGGGCGATGGCCCAGGCTTCCGATTGCAGTGAGCTCAGCACAGCGTCCGAGCCGGAAGTGCTGAATCTGATCCAGAAGGCAACTGCCATCTTAACCGTGTATGCCCCCAGAAAAAAGAATGCTGCCAGCATAAACAGACTGACCACGCGCGCCCGGAGCCTTTTGCGGAAATACAAAAAAAGCGCAGCTATCAGCAGCAGCGCACAGATAAAGGATATGGAATAAGCTATTAATAACACAATATCAATGATGCTCATCTTCTGCCCCCCGATCATAGATTAAGAACTCGGCGAACCCGTTGTTCCTGATTTCCTCCTGAATTTCTTTGGAGACATTCTTGTACCTTCGGATAGAGAGCGATACTCTCATTCCCGCTTGCGTCAGCTTCCGCTCTCTGTCCCGGTGCAGGGGGGATAACCGTTTGATCCACTCACTCAGCACGTTATCCCCTCCTGTCTTCTTCATTAATACTGCCTGAATTCTTGTCGCCCGCTGAATGATCAATCTTCAATCGCTGCAGTACTTCAAGTGTCGGTGCCATGAAGTCAGACCTCTCTTTATCGAGGATGTTCTGCAGCCTGTCCCTGTCTTCCTCGGCACGCTCCAGCAGTTCACGCGGCACCAGATTCCCCTTCACAATCGACCGCAAAAGCACAAGAAAAATCATCAGCAGAATCAAGGCAACAATATAGGCTAGTCCATACTTATCCGCCAGAGGCAGCAGCTTCTCCAAATTCGCAACATCATTGCTGTCCATTGCTTCACTCCCTTCTATGTTGGTCATTGATGCCCCCGGATGGGTCCGGGGGCAAAATAAAAACGCCTTGGTCGGCGCCTCTGGTTATCTATTCTTCTAGCAGTTTAGACACATCGGCGCGGATAATCTCCGGTACCTGCTTTAACGTCTTGAGGCCCTTACGAATCAAGCTTGCATATACTTCAGCCATTGTCTTCGTCACCTCCTTTAGTGGTCTGTTCTGCCTCCAGGCCAGTTTGTCCGGCTAGCATAAGCTCGTACAGCTCTGTGAGGGCTAATTGGGAGTCAGCTGCTTCTTGCCGAGTTACCTGCAATTCTTCGAAAGTTTCAGTGAGCGCGAGCTGAGTCATCGCCAGATCCAATTCGGTATTTGTTATTCGTTGTTCCAGCTCTATGACTTTCGGTGTGTAAGGATCGGCTGTCTTCGGTTCTTCATAATCATAATAGAGACGGGCATCCGTTAGATTCACCTTCAGCACCGGATCTTTCCCGTTATCTATAGGCTCAGGCAACACATCGACTGTAACCCCATCCACACCTTCCAGGGATTCCGTATCGTGGTACGTAGCATAAACGTACCCCACTCCGTCCCTTATATCATATGCACAAAAATAAGACATGTATTTCCCTCCTTAATTAGAATAGGTGATGCTTCCGGACAAACTCATTGTTGGGCTGTAACTATACGCCCAATCCGCTCTGAAATATAGGTTCAAAGGGGCGTCAGTGTTAAAATTAGCGGGGAGGTTATAGGTTGAGGGCGCAGTGCTTATCATATTCCCGCCGTTATATGTTGACGCGCTCCATATCGTAAGCGTTCGTTTTGCAGCGTCATACATCATTCCAGTTGGGTAAAGATAAAGGTTTCCTCCCCGTTCCATGTTTATCCAACCAACTTCAGCACCCGTCCAACCATCCTGCACAAATAAGGAAAAGCGTCCATAGTCATAGTAAACTGTCGATGAACCAGACCAGGTAAACCGTTTCGTTCCCGCTGGCATCGAACATATCAAATAAGCACGGCCATCCCCCGCCACCCAGCCGGAACTAAAGCTGATATCAATACGGCCGGATAGCGCTGGAGCCACGGTTCCATATACACCGAAGATCTCAGCACCTTGTGCAATGTACCATGGCTGTAAATGTGCATTCACACTTTTAAGCTGATCAACGCTAACCTTGATCTCCCCGGCCCCGGCTCCACCTTTCCGGTATCCTTCTCGTGGGTATACAGCAAGCGCTCCGTCTCCCCACTTACCTACGGAAAGAGCTACGTCCGCGCCTGTGGAGATTACCGGCATAGATCCCTGCATACCTAGAATAGAAACATCGGATCTAACATAAGCAGGATTAAGCCCGGAATCTTCGACTGCCACTGAAGCAATACCAGCACCAAAACCACTGTTCGTTAGGTAACCACCGGTGGGGAAACCAACCGCCACGCGCCCTACTCGTTCATAATTAACTCTTGCTGCCACTTGGTCATTTGCTCTGTTCGGCATCATTCCTGCTGTACCCGCGATAGTTGTTCCAGTTAGTACAGATGCAGCTGGAACCGAAACACCGGCAACAGTAATCGCTGTATCATAAATTCCTGCAGGCTTCACAACAGCCGAAGCTCCCGGCGTCACTGTCCCTCCCGTTTGCACCGCCAGCGTACCGGTTACATCACCCGCATCCGTTGCCGCTGTTTTTCCCGCGCGAATATCCCCGGCCACTGCGTTACCGGAGCCACCCGCGCTATCTGCCAAAAAATCCGTTCCTACCTTGCGGAACATATAGGGTTTGCCTGCAAGCAGCTTCCCGGCGGCGTATGCGATACCTTTTTGATCTTTTAATGGAATAGCTCCAAGACCGTTCACATTGAGTGTCGCGCCTGCTGTATTCACTAGATTCGGCACAATTGTAATACCGAATCCTTCTGGCAAACTCGCTGGTGCAGGGGTCAAATTTACAGTATAAGCTGCACCAGTACCTGCCGTTACTGAATAAGCAGGCTGCCGCACATAGTCCACAGTAGGGGACTTCCCATTTAACTGCCCCTGAATCCCCGAGGTCACCCCATCCAAATACCCGAACTCCGCATTAGACACAATCCCCGTCCCGATCTTCGTAGCATCAATCGCTGCAGTTGCATTAACGTCCGCATTCACAATTACCCCTGGAGCAATCGCCGTTACGCCATCCCCCGTGCTGGTTACATCCCCGGTATGATTGGGATGCACATAATTATTCGCCCCGGCAGCCACGCCATCCAGCTTTGCCTTATCCGCTGCAGCCATCAGACCTGCTGCGGACGCTGTGGCGGCGGCGGTGGATGCCTTGGCATTCCAGCCGGTGCGTTCAGCAGCCGTGATATGCTTAACTGCATCTGCGGCATGATCCTGCACAGCCTTGACGGCTGTGTCCAGAATATCCATATTGCCGTTCAAATCGGTTATATCTACAATGTCTGTACCATCCGGCTTTTTCAGCCCCAAATTCCCCGTTGTTTTCATCGCTCACACTCCTATTCGTATACTCTTAATTCGTTCCAGGTTCTGGCATGCGCACTATTCCAGGTAAGCGTCTTAACAGAGTCCCACCAGGTGTAGCTGTACACGAAGCTATAATCCAGATGTGCCGGTTTAATCTCCTCCAAGATCTGGATTAGACCCGCCATATTGGCCGGAATACCCAGCGTGCCCACGAAACGCACCTCGAAGCTGTACGCTCCGGGCACCTCCACCACCTCAACATCCCCGCCGGAAAAAGCGGATGCCGTCCGCCGGATCATCTCCGGAGTGGTCGTTCCGCTTCCCCGCAGCTTGGCCTTGATCATCTCCCGGCGGGTAGCATAAGACTTGTCCGTATCCGAAGTCAGTGCCAGCATCCGCTCCCAGCGGGACAGACTCCAGGTTGCAGACTCCAGAGTCTTCTGCGCATCGCTGTCAGCCATCGCATAGGCAAGCTCACCGCACTGCGCACCGGCACTCGCCTGCAGCTGCTCCATCTCAGGCACGCCCTGGTAATACTCCGGCAGGTACTTCATCAGATCCGGGACAATAACCTCCGGCCCCTCCCCCGTCACACCATCTGTTGAATATTCCAGAAGGCCATATATACTGTCTCCATAGGCCACGGCTACACCCCCTTAAGCTGATTCCAGGTTAGCGGACCTTTGGGCATATACTCATGCGTGTGCGCCGCCGGCGGGAATACGGATGGCTTGCCGTCCACACCGGACCAAGGCACACTATCCGCAGCCTGCGCGTAATCGACCTTACCGTTGTTATTGGTATCATAGATGCTCTTCAGCATGTCGCCGGTGCTTTGGGCGGCAACCAGCAGCAAATTGCTGCTGCCATTCCCAATGTAGAGCTTGCCTGTATCGGTGCAGTAGCCCAATTCGCCTGCGGCAAGCGTACCCAGTGCACTTTCCAGGCCGCGGCGGATTTGAATCAATGTCTTCAGTGCCATGGTCACCGCCCCCTAGAATGTTCCGCCATCTATACTGCCCACCGTCAGCCGGTTGCCGTTGCCCGCATCATACACAATACTGCTGCCATCCACATTGGCCGCAACCCCTGCCGCATCTACAGTAATGCCTTTGCCGGCGGTTACGGCAATCGCATCTGCACTTACCGTAATGCCGTTGCCTGCTCCGACATTCAGCGTTACCGCATCGGCCTGTCCGCCGCCGGTGAGCCCGTTACCCGCTGTAATGGTCTGCAGTGCTCCACCCGTCCGCACCCAGGCGGTCCCGTTCCAGCTGTATATTTTCTGTTCATCATCCACATATGCCGTCCAGCCAACAACCGGAACATAATACACCCAGACAGCAGACTGGTACTCGGCAACCTGATTGGTTTTCCCTGCCCATACACCCGTAGCTCCGGCCGGGATGATGTACCTTTCACCTTCAACCGGGCTGGCCGGCGGAGCGGTCAGATTCTGATCCTTGACCGAGGCCTGAGGCTCGATATTATGCTTGGCCAGCTCAATCTCATTTTTGATTTTTTGCGCAGACCACAGATCCGTAATTGCCGTCCCCGTATCATTGATCAACCGGTGCTTAGTGGCATCGTCGATATGGGTTTTGATCTCTGCTGCGGTCTTCGTATTGGTGCCGTCCGACACCTTATTGGGATGCCCCGCCGTGATATCCGCCTTGAGCACTTTGGCATAGGTAGTGCCATCTGCGATATCATCCACGGTTCCGGTCAGATCTGTTAATTTCTGCGCATTCACCCGGCGCCAGGCCGCCCCGTCATCGAAGTACAAATAACCGCTGTTACTTCCGCTGCTCACATAATACAGCCGGCCCACAGACGCTGCCGCAGGACGGGAAGCTTCCGGACCGGACAACGCCCGCCCGACCATGGAATTGGAGGTACCGTCTCCGATGTAAATCTCCTTCGTGTCTGTACAAAAGCCCATTTCACCGGCCTTCAGCGTCCCGTAAGTGGACAGCTCCGCCCGCGTACCGCGTTTCACCTGAATTGTTTGTGCCATTTTACACCTCTCTTTTGAAAGATCCGCCGTCAATCAGCCCGGCTTTTTTGTAACGTTCAAGCTCGCTTTGTGTAGCGGTCAGCCCCGACTGCAGCTGATTCACATCATCCGCTTCTACCGTATCTCCCGGCGTTTCGTAGGTCACGTACACTTCGGGCACATCGGCATAGATCTTAATCATCCGCCGCCAAGGCGCCTCATCAGGAAAAGACACTGAGTAATTCCGCACCTCAGTCCCGCTATAGCGTGAACCTGTATAGACGGATAGGGTCTGATTATTAATGTTATCGTGGGCAAGAAGCCCGCTGTACACACCGCCTGCAAGAAGAAGCTTCTCCTCGACGACATAGCTGCTGCCGTTTGCTTTTTTGTTCAGCCTATCCTGAAAGACGTCAATCTGCTCCGGATATCCCATCGCTACACCTCCAGTACGACACTGCCGAATAGCGGCACTTCAGTTTCGGTTAGAGTCACATTTCCCGTCCCGCCGTTCAGCTTGAGTCCGCTATAATCCACAACGCCGTCGGTATCCAGCAGCAGCGATCCAACTACAGATTGACTGATATAGGTGGCGGCAAAAGCTTTCTCTTTGCGGTATTTCTCCAGAATCGCTGTAAAAGCATTAATAACCGGCTGCAGCGCATAACCCGCTGCCAGTGTAACCTTGGCTGTGACGTTAATGGTTTTGCCTGTGGCGGATTCTACCGTCACTACGGCTCCGACCGGAGCTTGTCCTTCGCCAAGACCCGGAGCAGGATCGATATACTGCTGCACTTGAGAGACCAGAAGCGCGGAAGCAGGCTTGTGCTCCGCGTTCACAATGACCACTTTTACCGTCTTCGGCCCGGCCCACAGCGGAAAAACCCGCGCTCCCCCTACGCCCTGGATGTCCTGTGCCCATTCCATATAATGATATTTATTGCCGCTCGTCGAAGGCCGTCTAGCCGAATCGAAGTACCGCTGGCGCAGCGCTCCATCTGACTCCGCATCCGTACCGGGAACGAGCAGTGCCGTAATCTCCCCCCGGGCCAGCCCCGGGATATAATCGATGGGCAGCAGCGTACCCGAGTACTGATTTCCCTCTGAGCCGGCGGTCTCACTTTCGAGACGATACATTCCGGGTGACAGCTTCTCCGCTGCGCTATAGTGGAGCAAGCCCAGGGAAAACCGGCTGCCAAGAGGAATATCCAGCAGTTCCCCTCCGCTGGTATAGAACTTGCCGCTCAGCTGCGCTTTCCCTGCGGGATGGCGGGTAATCCCCGTCCAGGCAATGCTGCGTTCCAGATACTCACCACCCGCTGTATCGGGGAAATACAGATTATTGCTGACCTCAAGCTCAATATACATCTGGGCCATTTCGGCCGCCGCCGGAGCGAGCGCATCATAAATAATGCTTCCCTCGCGCTTATCCATCCCTTCCGGAACCCGGTCCAGCATACGTTCAAGCAGGGCCTCATAGGTCTGATCTTCATACACCGGCAATCTCCTCCTTTCTCAGTTCAAAATTGCCGTAATACGTGACAGCTGTGCAGCTGAAGCTCACCGTATCACCATTAAAAAGAATATCCACATCCTCAAGCTGCTGAATCCGCTCATCCTGGAGCAGCGCCTCACTTACAATTCTGCGCAGCTCCGGCCGGGCCAGCAGCCTGTCCTGTCCCAGTACGAGACTCCATTCCGTTCCGTAGTTTGGACTATAGATCAAATGCTCGAAGCGGGCAGTCTGCAGCACTTTGACCGCTGCCTGTTTCACTGCCTCGAGCCCATCAATACGTCCGGCTATCCGCTTATGCTCAAAGTCCATCCGGTACGTTAAGCTGGGGCTGGTACCCGAAGCTGCTGTACTCCCTTCAAGAGCTGCCGTAACCGGACCCGATCTGCCAATTGCCGGGATCATAGGTCCACCAGCCGATCCAGGACAATGTAGCTCTGTCCGCCCTGCATACGCACGAGCAGCACGCGGTCTCCCGCTGCCAAGCCCCGGCGGAGCAAGATCTCTCTGCCCTCAAACAATGTCCTGCTCTCCATCATGGACTCTGGAACAACCAGCGCCGGTCCGGTCAGAATAAACCGCTGCTCTACCTGGATCTGCAACGGCTGTGCCCCGACTACCGTTCCATAAGAAAAAGCCACCGGATTCGTATTCGATACGGCTCCGAGGCTTGCTTGTTTAATAATATCAAGCATGTTTGTCTACACCACCTTAATGTCTAGGGACATCGTATGCTCCCCTCCTGAAATCTTATGGCTGCATTGGTCCACCAGAAACAGCTGGGTCTCAAACTCATCAAGTAAGACATAGATGAAATTCCCGGCCCGGACCCGCATATCACCAATCGCCTGTACAGAGAGACTAAGCTTCTCGCGGTTATGCAGCTTCAGCAGATTGCCTGCCTTCTCCTGGATTTGCGCAGCATTCGCCTTGTCGTCCGCCTTCTGGTACAGATGAAGAATTCCCCAGCGTTCCACATTTTCCTTATCCGTTGCCGGGAAAAACTCACGTTTGCCGGTTTCCTCATTGTCTTGATAGAGCAGGATCGTATTGTACGTATCATCGTCAATGCTTCTTTTAAGCGAATAATCATACAGATAATGACCGGCACCAAGGATCACATTCAGCAGCATTGCCTGAGGCGCACGCAGGGTCAGCTTTCCGAAATCATCATAAAAAGCCATCAGCTGGCCCATATACTGCAGTTCGCTGCCGACTGCGCCCATAATAATATCGAGCAATTTTTTATTGTCCTCGATCAGGGAGGGGATCGTATACTTCGCCGGGTCCAGCACTCCGAGCCGAAGGCCATAGTCTGCGGCGACTTTGCGGATCAGTTCACTTGCAGTAATATTCTGCAGCACATAGCTGCCGTTGCCCAGCAGATAACGGATCTGGTCATAAGCCGTCAGCTTAATTTCCTGATTCGCTCCCGTATCGATGCTGAAGACGAATCCGTAGAACACATCAATCCCGTCTTTCCTGAACTGCACAATATCCCCGTTACTGATGCCGAACTTCGCATGCTGATAAATCCCGCTGTCCGCCAGCGTAAGCTCGAGTGTGGCAGGCTTTCCGGTACGTGTGGTTTTCCATGAGATATCAGTGGCAATCCCGGAAACATCCCAGATCGTGCCTTCTTTATTGATTACTATTAATTCCATCGCCATGGCCTCCTACGACAGCTTAATCACTCTGCCGGGTTTGAGCTTCTTCAGTTCACTGTCCGGGATACTGTTAAGCTTTTGCAGAGTTTTGCTTTTGCTGCCGTCACCCAGGTGCTTTTGAGCAATGGACCAGAGGGTATCCCCGGCTTTGATGGTATAAGTGGAGGGGGCTGTCTTCTCGCTTGCCCGCTTCTGCTGCGTCTTCACTTCACCCTTGCTGTCGACCTTCATGGCTAAGGCCTGATAGAACACATATTTTTTCAAGCCGATCGTATACTCGATATCTCCGGAAGAGCCCGCACTAAGCTTCCATGAGAAGCTTTCAATACTAACAGCCATATTGATGCCAATGTCCCCGGTAAAAGTCTGCTGCGCCTGCGTACTTGCCTGCTTCAGCCAGTCCGGAGTCTGCGTGTCCTGTACGTTCACTGCCTTCAGCCCTGAGAAAACAAACCGGACCGGCCGGCGGCTCAGCATCCATTTGCGGATCAGCTCCACATATTCATAAGGCTTCAGCAGCTTGCCGGCATTCTCGCCGGAATACACCACGAACGGATAATACTGTGCCGGAAAAATACTCTCAATGGTGATCTCCGTCAGCTTCGGATAAGCAATAGCATTGATCTCGCCAAAATCAACGACCGTATAGCTCTTGCTGTCACCGTTCTCTTTGATCTCAAGGGTCTCAGGGTTAACCGGAAGCCGGATCACCTCTTCATAGTTGTTGAAGCTAAGATAGAACCCATACTCTTCCACGTTACGTATACACCCCCTGGGCCGTAGAGACAAATTCCTCTTTCAGCTTTTGCCCGATCTTTGTAATGATGGAGTCAATATCGCCGGAGTTATTAATATTACCGGTTGTTACCTGCACAGTTGGCGTCAGCTCGACAAAATTCTGTATCGACTGAATCTCCGCTAGCTCCCGCAGCATATCCAGATCATCGCTGGAGATATCCACCTTTTCATTAATGGAACCTACTTCGCCCACTTTGTTGACGCTGTTGATGTTCGCTGCAGCGGCTTGAGCAGGATTCTGGGATTTATCATCTTTTGGCTTGACCCGATCCAGCTTGGTATTGAATTTTGCGGGGAGAGCTGATGCCTTGTCCCCATACTCCTTTACTGTTTTGGCGGTATCCACAAATTCTTTCTTTTTGGTATTGTACACATCCTTAGTTGATGTAGGCTCTACCAGGGTACCTTGAGCATTCTTAACCATATCACTGAAGACATGCGGATTCTCTGCTTCAAGAAAGTTGGGTTTGAAATCGGCCAGAAATTCAAAACCGGGAAATTTGCTTAACCACCCTGCCATAACTTGAATTCCCTTAAGTACAAAATTGATGCCTTCTGCTATAGCCTTTACGAACCCGCCTGCAAAGCTTTCAACACCTAACGCCATTTGGTAAATGAAGCCCAGGAAGTTCGTGGCCAGGTCATAAAATAGCTTTTGCACAGCATATGTCGGATCAATGAACAAGTTACGGAAGAAGTCTGCAAATGAAACGAAGTTATTATACAGACCGATAACAAAATTTTCTATCGTTGCCCGTAGCCAGCCAAAAGCTCCCCCGATAAAAGCCACTACCTCGTTTACGGACACACCTGCTTGTTGAAGAATGTAGATAAGCAGCGCTACAGCCGCAACAATTAAAAGGATCGGCCACATGCCTACAAGCCACGCGGCAGCAAGATTATATAACTGCACAATCATTGCAGCTATGAAGACAATGGCAATGGCCGCAAGTATCGGCCCTACAACATCCCAGTTCTCCTGGAACGCTGTAAACATATACAAGATGCCATTTACAACTTCTCCAATCACAGTAGCTATTACCAAGAATGCATTCGCGATCAGATTTAGTGCAGTAGACATTCCTTCAGATTGAAATGCATTATTCAAGGTATCCAGAATCGGACGCAACGCAACGATGGCTTTTTGACCCATCATTTCAACTGCGCTATCCATGTTGCCCTGCAGCTTGTTCCATTTCCCCTTATCTTCTTCCGTTGCGTTCGCAGCTATCGCTTTCGTACCCAGTGACTTAACCTTATCGAACACACCGCCAAGGTCCAGTGAACCCAAGGAATCCTTCGTCTTGGAGAGGAATCCCGGCTCTGCTGCTTTCCGCGCCTTTTCTGCTGCTTTTTGTTCCTTTTCTGCTGCAGCTTCTTTCTTCTTGTTCTGCATATATCCTATGGCTTTTTCCCCAACGTAAGTGATTAGTTCGAATCCGCCTACGTCCAGTGCCTTCATTATTTTTTGGACCTCACCCATAAATCCGCTCTTGGCATTCCGGACATCGTTATTATCCGGATCGTCATCGTTAGAACTGCCCGCGGAGCGTTGGGATCTGGAAGAGTCCCCTTCATCCGCCAGCCGTCTGGCTGCTTCCTGAGACTGCATGAACCCTTCCATAAAAGACTTATTTTTCTCCTCGTATATCCGCTCCAGTATCTGCTGCAGATCACCCAGCGAGTGGCTGGCCCGGTTAAAATTCTGGTTCAGCCGGTCCCACTGTGAATTCACATTTTGCCAGACGGTTAATGCTGTTACGGGAACCAATGCTGTACTCGTAATTTCCATTCATTCACCCCCTTCATCTCTTCTTCCCCTTGCTCCGGGCACGCTCCCGCTTCTCCTTGTCCACGCGCACAGCAATCATGGCATAGATCGCCGCACGTTCGCGGACGGAGAGCTTCATCAGCTCATGCGGCAGAATGTGCAGCTCGTGGAGGGCGTAGTAGGCCAGATTGGCCTCACCATCACCCTCGTTGATTAGTTTTTTACGTCATCTACCAGCTCGTTCATATCTGTGGCGAAGCCGTTAAGTGCCTGTACCCGCTCACCAAGCGCCGCAAATTCACCGGGCAGCAGCATTTTGCGCAGCAGTGATTCGGCCCCCATCACCCCATAAGAACGCTGCAGCTCGGTGTTCTTAAGATCCGGATGCACTACGCTAGCCGTCATCAGCTTCGCCATATACTCATTGGGATCAATCTCTGTAGAGTAGGTACCGTTCTTTCCTTTGACCTTGCGGGTAGCAGCTTTGCGGCATTCCTGGTTCTCATCCTCATTCATGCTGCGCAGCTTCCACACGGCAGCTTTACCTTCCTTATCCTTGAAACGAAGCGAGACCACAAACTCCTCTGTTGTATCGCATGCCGCATTTTGTGCAAAAAACAAACTTAATTCACTCATGTTGTTCCTCCCGGATTCTTATTTGTATTGACAAAAGAAGAGACCCGCCGCCATATAATACGCCCGGGTCTTTCCAGCTCTTGTCTATGGATATGCCTGCTTAATCTTTATTGGCCGGAATTTGCCGGGGCACTGAAGGGCTGTACCAATTCCACATCCTCAAATGTAAAGCTGACCTCTTCCTCTAGCGCATCCGACTCCGTATCCAGCGAGGCCATAATGACACTGTCCAGATTGACATCCTTCAGCATAATGCGCTGCGCGCCAACTGTAGAAGACGGGTCTTCATTCGTAACAATAATACTGAAATACTGGTCAATCCCTGTCTTCATATATTCCAGCATCATCTGACGGAAACGGCTCGTCATGTAGAAAATCGTCATCGTACCGCTGCCTGACCATCCGGTTGCCTTATGCTGCACCCCGCGGCGACCAAGCGTTTTCACTTCCGCCTTCTGCTTCTCCACCGTGGCTTCCAGCGTTTTTACATAGAACATTTCTTCCGTCTGTCCGTTAATTGTGGCATAGGCCCGGCCCTCCTGGCCGGATAGCGTATCGCTGGCTTTCAAGAATGTCATCTTAAACCACCTTCACTTTCATATATACTTTTTCTACGGAATCCACCGGCTTCACAGCCACATCCAGCACAACACTGTCACTGTCCGCTCCGGGGGTAACTACAATATCGCTCTGTGCGTTGAAGTTCTCAATTGCCCCTAGGTTCTGCAGATCATTCATATAGGTAACGCACTGCGACCAGAACAGCGCACGCCCGTCTTCATTATTTGGCAATTTGCCAATGAAGTAATTCTCAAAAATACGCTTCAAATCCCCGGCGATTCCATCCAGCACGCGCAGCACACGGTTTTTGGAGAATGCCTTACCCTTATCTGGTGAAAATGAAGTAAAGGTGTTGATATCCTGCTCTACCACAGCACGGCCGCCATTATACGTAAAGAGCAGTTCACCGTCTGTAAGCGCGGCTACGGTCTCGGAATGGCTGAAGCGCACATCCGCATCAACAGCGTCATCGTAGGCCTGATAAGTCAGGGATTCGTTCACTGCAGCGGCGGCAGTAGCACCGGCTACCCAAGTCACGGCATGCGCTTTATCCACCACAGTCCCGTCACTCAGCACCACACCGTTTGCCACGCTGATAATGCCCTCATGATCAGCTGTAGCATAATCGGACAATACCGCCTGCACCTTCTTGCCTTCCGTATTGCGCAGACGCTTCACATAAGCACTATATAGTGCCTTGAGCGTGTTATCCTCGGATACCAGACCCACAGTCTGGAAGTCCTGAACCTCCAGCGCCGACAGGAAGTCGCTGTGTTCCGTATTGGTTACCGTACCATTCGCACCGCTTACAAGCGGCATCCCAGCCGTTACCGTCAGCGCACCAGGTCCATTCGGTTTAAATTCTACATAGTCGTTTGCAGCCAGTCCGGCAGCCGTGGCTACTGTCTGCTTGTCCACCTCTGTATTCTCAAGCAAAGTCCGCACATCGAACTGAGCGTTGTCGTCGATATTTTTTTCGATAACAATCTTGAGTGCATTACCGCGTTCTCCGCCATACAGCGCCGTAGCCTGCACCCCGTTATTAGTGACAGCAGCCTTAACTCCCTGATTCAAGCGGTAGAGCAGCAGCGTACCTGCCCGTTTCAGCACCTCTCTTACCGGCAGCAGCTGCGCATCCGTCAGATCAAACCCTAGCTTCTGCTTGAAATCTTCCTGGGCAGTAAGCTTAAGAATGACTCCAGCTTGTCCCCAAGGCAGCGTAAGCGCCAAGGCCGCCGTACCGCGTTCCCCCATTTTACCTGCGACGCTTCCGTTTGAAGCCACATTTACGTATACTCCCGGACGCACCTTGTTTTGTGTTGTCCATGTTCCTCCAGCCATTAGATAACCTCCTTAGTTAGATAAAGCTCGATTAATTGCTTAGCCTCTTCCAGGGTGTAGCTCCCGCTCTCTTGCAGAACTACTTCCAGTACATCTTTTTCCTTCGGCGTGAATACGACAGAACCCATAATCTGCTTTTTACCAAAAGCATTCCGGCCTTCTCCGCTCCGCTTCAGCTCGCTTGCCTTCATTTCATTTGAACTCATTTCAGCCATGCTCCTTCTGTGAAGTGACCCATCAGTTCTGCCTCATCCTGCGGTTGTTTCTGCTTCTGGAGATAGAGCATATAGTCCACTGTGAACAGCGGCCCATGTCCCTCTGTTCCTGCCTCCCACGACTGGCGAATCACCCGAAAAGAAGAATTCCCGCTTTCCCTGACCGCCAACGCTTCACACAAACCGTCCGCCATACTCTCTGCTTCCAGCAGGCTTCCCTGCTCATAGCGGATACCGAAACGGTACACCGCCATATATCGGCCTTCCCGCTGCCGGTCGTACGTTGCCGAGATTAGCCCCGGTTTGAAGTAGGCTGACTGCGGCTTGTCCCCTTCCACATAGACAGGAATATCCGGATAAAACTGTGCCAGCGCATCTGTGATGTTCTCCCGCAATTGTTGTACAGCCATAATTTCATTCCTCTCAAGATTAGTTGTGATAATCCCTCCCCCCTTCTGGAAATCACAAACGGATAGAATCCTGACAAGAATAATATCCGCCTTGTATTAGGCAACTGCTGAAGGAACTTTCACCACGCTTGTGCCTAGCCCTCCAAGGGGCTGTATCTTGTAGAGCATTCATGCTCCTGCGGTGTCCTTCTGCTCCATTTGCCATGTTATAAATATAGACCCTTTGAATCCTTGCGCAGACGCTATTACAGAGGAGAAAGGACTAACTTCCGGAGACCCTTGGGATGACAAAAGGATGTACCTGCGATCCCGCAAAAAAGCCGCATCACCCATTGGGCAACACGGCTTGCTGTATTTCTTATTATCTAAAATAACCGAATCTCCAGGCTATTACTGTGGAACGGTTAAGCTACAGAAGGCTGTCTGCTATTTCTCCCTGCTGGCCCCTGTTGTTTTCTCTAGCGTAGCTAATGATAACAGCTGCAGATCTGCGAGCGCGAGCGCCATCTTATAGAACGCCTTCGACCTTATTTTCACATAAGTGTCCTTACTCACCGGGGGATCGAACACATGATTATAGATCGTGTAGTCATAGCTCTCCTCTCTGCGCATATAGCGCTCCCGTACAAGCTGCTGTTCTCTAAGTGTAAGCCTCTCTACTACGGAATCTATCATTGCACAATATGCTCTTCTTGCAGCAGGCACATCCACGTTATGAGTTGCTATGGCCGCCGTCTGATCCGTAACCGAATTTGTCGCGCCATGGAATCTCTCCATATAAGAGTACGTAATCCCGGCCTCTTTAGCCTCGAAAGTTACAGTCTTAAAAATACGGTATTTCTCCAGCATATTCTCTATAGTGACCTGAGTAAGACGGCGGTCAAGCTCGGGCAGCGAAGCTAGAATCATCATGTGAACCACTCCTTTGATGTTGAACAGATTTGAGAACTTTATTGCGGACCTTTGCAGCGAAATGTGGTAGAATTTTACTTGTTCGTATATTGTTCGCCTTTTTCAATAATATACCACTTATCTGCCAATTCCGTAAAATCCCATTTAAGCCCGTTTTAGTGCATAAACAAGCTATATTCATCACTTCTCTTACCTTTTGGCAACAATGGCTGCTTTATTGTTTACCTATTGGCAAAAATAGCTTATATTAATAGCAACAGCTTATTAGGTGATAAGGAGTGGTTAATGATGGCAGAGGAATTTGGGAACTATCTGAAACAGCTTCGGGAAGACAAGGGGCTGACAATCAATCAGTTGGCATCCCTTGCCGGAATCAGCGGAGCACAAATTTCGCGGATAGAGAATGGATTACGGGGTGTCCCTAAGCCGGCCACATTGCGTAAGATTGCTGATGCGACCGATGTCTCTTATGAGGAGCTTATGGGCCATGCCGGTCATTTAACGGAATCTGAGAGCAGTACAGAAGGTGCAGTGCCCGCATGGGCTACGAGTAAGGATAAACGGGATTTCCGCCAAATGCTCGAGGATGACGGTGAGCTGATGTTTGACGGAATCCCTCTGAACAAGGAAGATAAGCAGCGGATCAAGGATGTATTAACAGGTCTATTCTGGGAGGCCAAGCAGATGAACAAAAGAACCAAGCCCAAGCACGATTCAGGTACGAAGGAATAGCCAGGCAATCATACAACTATTAACATGCTGCGGGTGAAGAATATGGATGAGCTAATTAAGCGTCTGGTCAAAAAATATAAAACCAACAGCCCCTTCGAGCTGGCTGGGGCCCTCGGCATTCACATCAGGTTCATGAATCTGGGCGAAGGCACCAAGGGCTTGTATTACCGTAAGCTAAAAAGAAGGTTTATTGTCATTCATAATGAGCTGCCTCTGGAGTGGCAGCGGTTTGTATGTGCGCATGAATTGGCTCATGACCGTCTGCATAAAGGGGTCAACCGGTTTTTTCTGGAGGAAAATTCTTATTTCTCTTCGGGGAAGCTGGAGCGTCAGGCAAACTTATTCGCAGTGAAGCTGCTATCCGCCGGCACTTCTATCGAGCAGGAGGAATCTTTACAGAGCTATTATGCAAGGATTGGCATCCCGGCAGAGGTTGTCTTTTTTTTAGATGATTAAAGGAACATACGTTCCTTTAATAACGCAACAAAAAACTCTTACCGAAGTAAGAGTTCATTGCCAGCTATAAGCTGAATTATCGGGATGACACGATTTGAACATGCGACCCCCTGGTCCCAAACCAGGTGCTCTACCAAGCTGAGCTACATCCCGAAACTATGAAATTTAATATGGAGCGGGTGATGGGAATCGAACCCACGCTATCAGCTTGGAAGGCTGAAGTTCTACCATTGAACTACACCCGCAAAGGTGAAATATCGGGATGACACGATTTGAACATGCGACCCCCTGGTCCCAAACCAGGTGCTCTACCAAGCTGAGCTACATCCCGTTAATATTAGGGCTATAATACAAAATAATAATGGCGCATCCTGAGAGGACACTTTGATGATTCAATGAAGTTATAAATGGCGCGCCCTGAGAGATACGGATGCTGCGCATCCGATTGCGAAGAAGATGCTATCGAAGCTTATGCTCCAACGAACTCGTTCGAATCTTGAGGACACTTTGATAATTCAATGAAGTTATAAATGGCGCGCCCTGAGAGATTCGAACTCCCGACCTTTTGATTCGTAGTCAAACGCTCTATCCAGCTGAGCTAAGGGCGCAAAAATTATGGAGCGGACGACGGGAATCGAACCCGCGACCCTCGCCTTGGCAAGGCGATGCTCTACCGCTGAGCCACGTCCGCAAATAAGTGGTGCGCGTGAAGGGACTTGAACCCCCACGTCTTACGACGCCAGATCCTAAGTCTGGTGCGTCTGCCATTCCGCCACACGCGCATAAAACTGATAAAAGTGAGCCATGAAGGACTCGAACCTTCGACACCCTGATTAAAAGTCAGGTGCTCTACCAACTGAGCTAATGGCTCGCAATTGGCAGGGGATATAGGATTCGAACCTATGATGACGGAGTCAGAGTCCGTTGCCTTACCGCTTGGCGAATCCCCTACAATAGATACCTATATAATGCCCACAATCTCCCACAAATATCAAGAAAATTATGGTGGAGGCTGAGGGGTTCGAACCCCCGACCCTCTGCTTGTAAGGCAGATGCTCTCCCAGCTGAGCTAAGCCTCCATATGTATGGCGCTCCAAAGGGGCATAAAAATTGGTGACCCGTATGGGATTCGAACCCATGTTACCTCCGTGAAAGGGAGGTGTCTTAACCCCTTGACCAACGGGCCTTAGTAAATCTGTGGAGCTCTCAACCGGATTCGAACCGGTGACCTCTTCCTTACCATGGAAGCACTCTACCTGCTGAGCTATGAGAGCATGGCTCCCCGAACAGGACTCGAACCTGTGACAACTCGATTAACAGTCGAGTGCTCTACCAACTGAGCTATCAGGGAATATTATCCGCTTGGCGGCGTCCTACTCTCCCAGGACCCTTCGGTCCAAGTACCATCGGCGCTGGAGGGCTTAACGGTCGTGTTCGGGATGGGTACGCGTGGAACCCCTCCGCTATCGCCACCAAACATGATTTTTCGAAGCTTCCGCTTCTCGAAATCGCTGCAAGAAAAGATCAGTCCCCAGAAAGGACATGCAGCTTAAGGTGTACCAGGCTTGATCGCCTGAAAACTGAATCCGAAACGAATCTGCGTTGTAGATTTTTGGATAAGCCCTCGACCGATTAGTATTGGTCAGCTCCATGCATTGCTGCACTTCCACCTCCAACCTATCTACCTCGTCGTCTTCAAGGGGTCTTACTAATTGGGAAATCTCATCTTGAGGGGGGCTTCACGCTTAGATGCTTTCAGCGCTTATCCCGTCCGTACGTAGCTACTCAGCCATGCTCCTGGCGGAACAACTGATGCACCAGCGGTACGTCCATCCCGGTCCTCTCGTACTAAGGACAGCTCCTCTCAAATTTCCTGCGCCCACGACAGATAGGGACCGAACTGTCTCACGACGTTCTGAACCCAGCTCGCGTACCGCTTTAATGGGCGAACAGCCCAACCCTTGGGACCTACTTCAGCCCCAGGATGCGATGAGCCGACATCGAGGTGCCAAACCTCCCCGTCGATGTGGACTCTTGGGGGAGATAAGCCTGTTATCCCCAGGGTAGCTTTTATCCGTTGAGCGATGGCCCTTCCATGCGGTACCACCGGATCACTAAGTCCGACTTTCGTCCCTGCTCGACTTGTAGGTCTCGCAGTCAAGCTCCCTTATGCCTTTGCACTCTGCGAATGATTTCCAACCATTCTGAGGGAACCTTTGAACGCCTCCGTTACTCTTTAGGAGGCGACCGCCCCAGTCAAACTGCCCGCCTGACACGGTCCCCGTACCCGATTAGGGCACTAGGTTAGAACCTAGATACGATCAGGGTGGTATCCCAACGGCGCCTCCAGCGAAGCTTGCGCTCCGCTCTCACCGGCTCCCACCTATCCTGTACAGATCGTACCCAAATTCAATATCAAGCTGCAGTAAAGCTCCATGGGGTCTTTCCGTCTTGTCGCGGGTAACCTGCATCTTCACAGGTATTAAAATTTCACCGGATCTCTCGTTGAGACAGCGCCCAAGTCGTTACGCCATTCGTGCGGGTCAGAATTTACCTGACAAGGAATTTCGCTACCTTAGGACCGTTATAGTTACGGCCGCCGTTTACTGGGGCTTCGGTTCACAGCTTCGGATTGCTCCTAACCACTCCCCTTAACCTTCCAGCACCGGGCAGGCGTCAGCCCGTATACTTCGCCTTGCGGCTTCGCACAGACCTGTGTTTTTGCTAAACAGTCGCTTGGGCCTTTTCACTGCGGCCCCCTCGGGCTATTCACCCTACCGAGGCACCTCTTCTCCCGAAGTTACGAGGTCATTTTGCCGAGTTCCTTAACGAGAGTTCTTCCGCGCGCCTTAGAATTCTCTTCTCGCCTACCTGTGTCGGTTTGCGGTACGGGCACCTTCTCCTGGCTAGAGGCTTTTCTTGGCAGTGTGAGATCATGACCTTCGCTACTACAATTTTCGCTCCCCATCACAGCCCAGCCTTAACGGTGTGCGGATTTGCCTACACACCAGCCTCACTGCTTAGACGGACATCCATCAGTCCGCGTCACTACCCTCCTGCGTCACCCCATCGCTCATAGCGGATTACGGTGGTACAGTAATTTCAAACTGTTGTCCTTCGACTACGCCTTTCGGCCTCGCCTTAGGTCCCGACTTACCCTGAGCGGACGAGCCTTCCTCAGGAAACCTTGGGCTTTCGGCGGATCAGATTCTCACTGATCTTTTCGTTACTCATACCGGCATTCTCACTTGTATGCTGTCCAGCGCTCCTTACGGTACACCTTCAACCCACATACAACGCTCCCCTACCCCAGATGCAAAGCATCTAGCCATAGCTTCGGTGGTGTGTTTAGCCCCGTTACATTTTCGGCGCAGAGTCACTCGACCAGTGAGCTATTACGCACTCTTTCAATGGTGGCTGCTTCTAAGCCAACATCCTGGTTGTCTGTGCAACTCCACATCCTTTCCCACTTAACACACACTTGGGGACCTTAGCTGATGGTCTGGGCTGTTTCCCTTTTGACAATGGATCTTAGCACTCACTGTCTGACTCCCGGCAAGAAGTTAATGGCATTCGGAGTTTGACTGAGCTTGGTAACCCTTGCGGGCCCCGCACCCAATCAGTGCTCTACCTCCACCACTCCATTCACCGAGGCTAGCCCTAAAGCTATTTCGGGGAGAACCAGCTATCTCCGAGTTCGATTGGAATTTCTCCGCTACCCCCACCTCATCCCCGCATTTTTCAACATGCGTGGGTTCGGGCCTCCAGTGCGTGTTACCGCACCTTCACCCTGGACAGGGGTAGATCACACGGTTTCGGGTCTACGTCCACATACTCAGTCGCCCTATTCAGACTCGCTTTCGCTGCGGCTCCGGCTTCTCACCTTAACCTTGCATGTTAAACGTAACTCGCCGGTTCATTCTACAAAAGGCACGCCATCACCCATAAAGAGGGCTCTGACTTTTTGTAAGCACACGGTTTCAGGTTCTATTTCACTCCCCTTCCGGGGTGCTTTTCACCTTTCCCTCACGGTACTGTTTCACTATCGGTCGCCAGGTAGTATTTAGCCTTAGCAGATGGTCCTGCTGGATTCATACGGGGTTTCACGTGCCCCGCACTACTCGGGATCCGTCTCGGAGAGAACACAGTTTAGGCTACAGGGCTTTTACCTCTATCGCGGGCCTTTCCAGACCTCTTCGCCTACCATATTCCTTTGTAACTCCATGTGAGACGTCCCACAACCCCAAGGGGCAAGCCCCTTGGTTTAGGCTGTTCCGCGTTCGCTCGCCGCTACTGACGGAATCACTATTGTTTTCTCTTCCTCAGGGTACTTAGATGTTTCAGTTCCCCTGGTCTGCCTCTGCGTATCCTATGTATTCAGATACGAGTAACTGCGAATTACCACAGCTGGGTTTCCCCATTCGGACACCCCCGGATCAAAGCTTGCTTACAGCTCCCCGAGGCAGTTTCGTTGTTCGCCACGTCCTTCGTCGGCTCCTGGCGCCTAGGCATCCTCCGTGTGCTCTTATTAGCTTAACCGTCACTCCGGTGTTTCGCTTGTTTGCTCATCTTGTTTTGAATGCTGCTCATGGATTGCTCCATTCACCAACACATTCAAAGCCAAAGGTCGCTGCACAATCGAAAACCTTCGTTCTGCACTAATAACTATTCCAACTTGCTTTCACAAGTTTCAGCTAAAAGATGTTCTAAAACGCAAATTCGTTTCGGTATCCAGTTTTCAAGGATCAAGTTCTTGCATATACTCTTGTAAAGATAATTGGTGGAGCCAAGCGGGATCGAACCGCTGACCTCCTGCTTGCAAGGCAGGCGCTCTCCCAGCTGAGCTATGGCCCCATAAAGGTGTTATTCAAATCTAAAATGTTATATGGTGGGCCTTGGTGGACTCGAACCACCGACCTCACCCTTATCAGAGGTGCGCTCTAACCAACTGAGCTAAAAGCCCATATAACAAATAACATGTTGAAGCAACCAATAAATTGATTGTTCGCTTGGCGGCGTCCTACTCTCCCAGGACCCTTCGGTCCAAGTACCATCGGCGCTGGAGGGCTTAACGGTCGTGTTCGGGATGGGTACGTGTGGAACCCCTCCGCTATCGCCACCAAACGCATACGAAAGAGACTTGCTCTTTCAAAACTGAACACGAGTGAGTGTCCGAACCCGAAGGTTCTATTGTGGAAGCTTTAGCTTCCGATTTGAATGTCACCGTTGCAGGTGACGATTCTCCATAGAAAGGAGGTGATCCAGCCGCACCTTCCGATACGGCTACCTTGTTACGACTTCACCCCAATCATCTACCCCACCTTCGGCGGCTGGCTCCCTTGCGGGTTACCCCACCGACTTCGGGTGTTGTAAACTCTCGTGGTGTGACGGGCGGTGTGTACAAGACCCGGGAACGTATTCACCGCGGCATGCTGATCCGCGATTACTAGCAATTCCGACTTCATGCAGGCGAGTTGCAGCCTGCAATCCGAACTGAGACCGGCTTTGCTGGGATTGGCTCCGCCTCGCGGCTTCGCTTCCCGTTGTACCGGCCATTGTAGTACGTGTGTAGCCCAGGTCATAAGGGGCATGATGATTTGACGTCATCCCCACCTTCCTCCGGTTTGTCACCGGCAGTCACTCTAGAGTGCCCAGCCTTACCTGCTGGCAACTAAAGTCAAGGGTTGCGCTCGTTGCGGGACTTAACCCAACATCTCACGACACGAGCTGACGACAACCATGCACCACCTGTCTCCTCTGTCCCGAAGGCCGCCGCTATCTCTAGCGGATTCAGAGGGATGTCAAGACCTGGTAAGGTTCTTCGCGTTGCTTCGAATTAAACCACATACTCCACTGCTTGTGCGGGTCCCCGTCAATTCCTTTGAGTTTCAGTCTTGCGACCGTACTCCCCAGGCGGAGTGCTTACTGTGTTAACTTCGGCACCAAGGGTATCGAAACCCCTAACACCTAGCACTCATCGTTTACGGCGTGGACTACCAGGGTATCTAATCCTGTTTGCTCCCCACGCTTTCGCGCCTCAGCGTCAGTTACAGCCCAGAAAGTCGCCTTCGCCACTGGTGTTCCTCCACATATCTACGCATTTCACCGCTACACGTGGAATTCCACTTTCCTCTTCTGTACTCAAGTCACCCAGTTTCCAGTGCGACCTCAGGTTGAGCCCAAGGTTTAAACACCAGACTTAAATGACCGCCTGCGCGCGCTTTACGCCCAATAATTCCGGACAACGCTTGCCCCCTACGTATTACCGCGGCTGCTGGCACGTAGTTAGCCGGGGCTTTCTTCTCAGGTACCGTCACTCCGGTAGCAGTTACTCTACCGGACGTTCTTCCCTGGCAACAGAGCTTTACGATCCGAAAACCTTCATCACTCACGCGGCGTTGCTCCGTCAGGCTTTCGCCCATTGCGGAAGATTCCCTACTGCTGCCTCCCGTAGGAGTCTGGGCCGTGTCTCAGTCCCAGTGTGGCCGTTCACCCTCTCAGGTCGGCTACGCATCGTCGCCTTGGTGAGCCGTTACCCCACCAACTAGCTAATGCGCCGCAGGCCCATCCCCAAGTGGCAGATTGCTCCGCCTTTCATTCTCTCTTCAGGAGAGGAAAGAAATTATCCGGTATTAGCTACCGTTTCCGGTAGTTATCCCAGTCTTGAGGGCAGGTTGCCTACGTGTTACTCACCCGTCCGCCGCTAAGCAAGAATGGAAGCAAGCTTCCATTCAAACTCCGCTCGACTTGCATGTATTAGGCACGCCGCCAGCGTTCGTCCTGAGCCAGGATCAAACTCTCCAAATTGTATTTAGAAAGAGCGATTGCTCATTTTGAAACATCTGACGAGAACTTACATTCTCTATTTTGGATCTCGCCGAAGCGATTTCCCACTCACTCGTTGTTCAGTTTTCAAAGATCAATGTCTCATTTTAGCTCTTCACCGCATCTCAGCGGCGACCTTTATAATATATCATAGTGTTTCGTTGTTTGGCAAGCTTTTTTTGAAAAAGTTATTTTTCATTATTCCCTGCCTGCAGCATCCCTTTAAACATTCAAAAGGAGCGCGAGATATAATGTATCATGCCGGCTCCCTTTTAGTCAAGCTATTAGGTTAATTTTATTTACTCTGATCTTATACCACTTTAGAATTCAATGTTTGAATTGAGAAGAACGTCCTCCCCATGCGTACTTTGACAACTCCTTCTGTGGTGCAAAACGTGCATACATACGGAATACGGTTTTATATCGATTGGCAATAGCGTGTCTGATATTCTGATCTAAACGCTGATCGCTCAAATCCAGAAGCATTTCATCCAGCTCTTTGCGCAAAACATAGTCCAGCTCTTTGCATTCCTTCTCATTGAACAACATCCCGAGCATATGCTTGGCCTCCTTCATGAAATTCATAGCTATCAACAACCATCAAATGCCATGTCCTCTACTGTAGAAAATAGACCATTCGATGTGGGAAGCTCCTATTGTACTGCTTACACTAGATTAACCGGAGCATAGGATCTATAACCATAATTATATAAAATTCCATTATGGTTTCGTTATATCCAAATTCCGACTATGGGGCCAATCTATTTGGCTTTTAATGTTATGCTCAATTCCCATAAATTTTATGATAAAAGTGAAAATGTAATTGTACTCTCAATGATTGCCGCGATGAACAGCAGAATAACAATCCATACCGAAGCGGTAAAAGTCTGCCGCATGAACGCCTGCCAATGGTCTGCTTCCCTCTCATTCCTCTTTCCCGCCCGAAGCAGGGCAGATAACGCTTTGCCTCCGAATCTCAGACCAAAGGCACAGGCAATAATGATTGCCGGAATCTCGATAATCCCGTGCGGCAGCAATCCTTTTACAATCAGGGTGAACAGGTCCTGTCCCTGTATTGCGGACAAATGAATCAGATAACCAATGACCGCACCATTAATCAGCAGGAAGAGCACCGGCAATATTCCAAACAGCGCCCCAAGAAATATAATGACCACGCTTTTGATGCTATTGTTCAAGAATATGAATACAAAAAAGCTCCACTGCGGATTGGAGGACTCTCTAAGGTCCCCGCTGATTTCGCTGATTCCTTTCAATTGCTCGTTCAGCAGCTGCTGCAGACTTCCTGTACCGATCCAGCCTATTACACCGCCGGCTATGAATAACAGGGCTGCGGTCAGCAATGCTTTGCGGATCGTCCCCAAGTCTCTGATAAAAGTATTAAAGGATAACATGTGTACCTCCTGAAATGATATCGCGCTTCAAAAGCATTTACTGCGGTTTCATATCTGCGGTCATAAGCGCCCTGTACGAGCATACATTTAGAACAAACAAGCATTTCGCATGGGAGAGGAGCGCTGACATTATGAATTCTTTTTATGTATTCAGCGGCAAAAAGATAAAACGGTTCATTTACATCTTTGCTGCTGCGCTTCTTACCGCCGGCGTCGTCTATGTCGAGAGGGGTAATATTACTGTTTTCTCGGAAGCAGCCCCTTCCGCCATTTACAGTGTGCCGACGGAAAAGAAGCTGATCGCCTTAACCTTTGATATTAGCTGGGGGGAAAAGAGACCCGAACCAATTCTGAAGGTGCTGGAAGATAAAAAGGTGGATAAGGCTACCTTCTTCCTGTCCTCCCCTTGGAGCAAGACCCATCCTGAGATCGTCACCAGCATCAAAGACGCCGGATATGAGATTGGCAGCCACGGCCACAAGCATGTGAACTACAGCACGCTGAGCAATGAAGAAATCCGTACGCAAATTACTACTGCCCATACGGTATTGACCGAACTGACGGGAACACAGCCTAATCTGATTAGAATGCCCAATGGCGATTTTGACAAAAGAGTGCTTCAGGTTGCCTCTGATCTTGGTTATAAGGTCATTCAATGGGATACGGATTCGCTGGACTGGAAGAACATCGGTGTGGATAATATCGTGAACCGTGTGACGAGCAAGGCCCATCCCGGAGATATCGTTCTGCTGCATGCCAGCGACTCCTGTAAGCAGACTCATGAGGCATTGCCGCAAATCATTGATAAGCTGCGCAGCCAGGGATATGAATTCGTTACTGTCTCTGAACTAATCAGCCAAAGCAGCGCCGACGGCAAGGAAGTCCGCGACTCCGCTTGGCTGGATAATGGGTTAGAAGACGCTGCCGGGATGTAAGCTTAGGCCAGTTCTATATCGCGCCGTTATAGTGTATGATGCAATGAATTAGTGGCGCGGAGAAATAAGCTCGGAAATATCCGGAGTAGGTGTATTTAGTTTCGGGTAACTCAGGTCAAGCCCCTCCAGCGTCTTCACCACAATGGCCAGCGCCAGATAATTGCGGTACCATCGGTGATTCGCGGGAATCCAGTACCAAGGGGCTTTCTCTATGCTGCTTTGCTCAAAAACATCTTCATAGGCCTTTTGATAATCGTCCCAGTATTCGCGCTCCTGCAGATCACTGGCATCGAACTTCCAATGCTTCGCCGGATCATGAAGCCGCTCCTGAATCTTCTCCAGCTGTTTCTCCTTGGAGATATGCAGAAAGAGCTTGATGACCGTTGTCCCCTCTTCCGCCAGCATTTCCTCAAACTGGCGGATGTAGCGGAAACGCCGCTTGGCATCCTCTTTCTTCAGACTGCCATGCACACGCGGTACCAGTACATCTTCATAATGCGAACGGTTGAATGCAGCGATATAGCCTTTGGGTGGTGTCTTCATATGGACTCTCCACAGGAAATCGTGAGCCTCCTCCTCAAGAGAGGGCTTCTTGAAGCTGGTGACGATGAACCCCTGCGGATTAATGCCGGAGAAAATATGCTTAACGGTTCCATCCTTCCCGCTCGAATCCATTCCTTGAAGAATAACCAGCAGGGAATGCTTCTTCTGTGCAAAAAGGATATCCTGAAGCTCAGCCAGCCGTTTCTTCAGCTTCTCCATTTTGGCTTCCGCTTCTTCCTTGGATTTGAATTCACCGCGTTCATTTGGATCGAGGTCCTTCAGGCGTGTTTCACTTGTGTCTTTTATCATATAACGCTTGATGTTCATATATTCCCTCCTCCACTCTGTTCTTTAAGATTAACCTCTTGAAGTTGATTTTAACCGTTCCGCTCAAGCAATGCCAAAACCCCGCCTCTCTGATTGTATTCAGAGGGACGGGGTTTTGGTTTATGGATATTTTAAATTGAGGCCGGTTTCAAAACACGGTGCAGCATCAAAATTTGGAACGCATTGCAAGCGACCAGCGGAACAAGAATAAAAATGGTGGCGCTGTCTACACCGATCCGGAGGACGCCGATAATTTCCACAATGGTGATGGCGGTCATAAAGAAAAAAGTTGGAATCCAGGCCGAAGCGTTAGTCCCCCGCATTTTGAACCCGGAAACAACAATTGCTGTAAGCAGAATTCCCACTCCCAGAATCAAATCAGATGCAACACTGCGGTCTCCGCTTACAAAGGTACGCAAGAAAACCAGTTCAAGCAGCGCGAGCACGGCCAGCACCAGTTGTATGTACCGCCAGGCCTTGCGCGGGAATACGCCAATGCCCATGTAGTTAAGAATCAGATAAGCGAAGAACCCAAGCTGGGCATATACACTGACGAGCACTCCATAGCCAAAAAGGATCAGGGCGTAAAGTAAAAGGTCGGCGGTGCTCTTGAAATCGATTCCGCCATTCACTGTCTGCAGGGCAAGACCGGCAATTACAGCCCCTCCTGCTCCGATCAAAAGCGTGGTCCAGAATAAATAAAACCATTTTCTTAAGTTCAGCGCTTTCACCTCCCCGTGTCAGATTTATTTTACCAAGGTTACCGTCAAAAAACCATTACACTCCAACATAAATGTGTGTCCCCGCGGCATACTACAGTCAGTAACTCTATAAAGGAGGGCAGCGCCAATGAAATGGAGGACTTTGTGGTCTGGAGGCTTGGCACTCGGCTTGGTTATGGCCTTAACGGCCTGCGGAGGCGAACAGAGCAGTTCTTCTTCCGGACAGGGCGGATATAAGGAAATGAAGACGATGGTTGTAGATATATTGAAAAGTGATGAGGGAAAAAAGGCGGTTGAAGAAGCCCTTTCTACCCCCAGCTCGGGTGAAAGCAGCACAAGCGGGCTGAGCATGAAAATGATGCCCATGCAAACCACCGAGCAGATCCGGATCGCGGTTAAGGATACGATCACAGCTCCGGAGTACCAGAAGGAAATCGAAAAGATCATGACGGACCCGCAATTTGCCGGGGAGTTCGCCAAAGCGATTAATACGCAGAGCAAGGAATTGCATCTTCAATTAATCAAGGATCCCACTTATCAAAAGTCCGTCGAAGAAATCATGAAGTCGCCTGAAATGATGAAGATGTTCCTCGACCTTACTAAGACTTCCGATTACCGCAAACAGTCCATGACCATTATGCAGGAGGCCATGCAGAATCCGCTCTTCCGGATGGAGGTGCTCGACCTGCTCAAATCTGTAGTCCAGGAAGAGCTGCAGCCTAAGGTACAGAAAAAGGATGCGGAGAAAAGCGGCGGAGAGGGACAGGGAAGCGGAGGCGACAGTCAGAAGCAGGAAGGCGGAGATGATTCCGGCTCTTAAAATAACATATATATTCTTTTCAAAAAAGGCCTTGCCCCATATGGGACAGGCCTTTTTGTATGAGACACGCCGGCATTACTTACTGTTCGTACTTGGCGATTAACTTGTCTGCAATTTCTGCAAACAACCCTCCGGTTGGCGTATCCGCCTTATACACCGACGGTGAGAAATCAGGCTCAGAAATATGGTTGTCCGGTGCTCCAAGCGGCACCTGGGCCAGCAGCTCCGTATGCAGCGTTTCGGCCAGACGGGCCCCTCCGCCGCGTCCGAAGATATAATCCTTCTTCCCGCAGGAGGAACATTCGTAATAGGCCATATTCTCGATAACCCCAAGAATCTCATGCTCAGTCTGCAGAGCCATAGAGCCCGCTCTTGCTGCCACAAAGGCCGCCGTAGCATGAGGGGTAGTTACAATGATCTCCTTGCTGTGCGGCAGCATCTGATGCACGTCAAGCGCCACATCGCCCGTTCCCGGAGGCAGGTCCAGCAGCAGATAATCCAGCTCACCCCAGCCTACATCGCTGAAGAACTGGCGCAGCATTTTGCCAAGCATCGGCCCTCTCCAGATCACCGGACTATTCTCCCGGATGAAGAAGCCCATCGACATGACTTTCACTCCGAATCGCTCCACCGGAATAATGACGCCTTCTTCCACAATTGGCCCTTCTTCAATGCCCATCATATCCGGGATACTGAAACCGTAGATGTCAGCATCGATCAGACCGACCTTTTTGCCCTTTCTGGCTAGTGCTACGGCCAGGTTCACCGTCACCGTTGACTTCCCCACTCCGCCCTTGCCGCTGGCGATAGCGATGAAGTTCACTCCTGAGTTCTCATTGATCAGCTCATGCCCCTCAAGGCCCGCTGCATGACCTTTCAGCTTCTCGCCTTGTTCTGGTTCCTGCTCGTCCTCTGCACTCTCTCCGCGGAGTATAGCCCGTTCATAATCGGTGGCATCACGCAGACGGATATGCACATTCCCTGCATGAGCCGCTGCAAGCAAATCACGGACCTGCTGCTCCAGCTCCATGCGCTTCTTCTCATCGGTATCGAGACATACGATGGATAGTGATATCCGGTCCTCTTTAATCATGATATCGCGGATTAACTGTAATTCGACAAGGCTTTTTCCGGATTCCGGGTCTGTGAGCGGCTGCAAAAGTTCCTGAATTTGTTCCCTAGTCAGCATGGAAAGCACCTCTGTTTCCTCTCCGGCGGGTAAGCTCCGGTATTTTCGTCTATTATAGCATTACCCTCCGGCGGAAGAGTAGTCCCACCCTATGGCTGCTCAGAGGTATACCGCAGGATCCCCCGGTAGATACTGGTAGCCACCTTCCGCTGATACACATCATCTCCGAGCAGGGCTGATTCTTCAGGATGGGATAAGAAACCTACTTCAACCAACGCCGCCGGCATTTTTAATGCTTTTAGCAAATATACGGTATTCACGGTCTTGGCCACACGGTCTGTATTCTCAAGTGTAGCCCTCAGCTCATCCTGTACCAATCCGGCCAACGCCTTGTTGCCCTCATTGCTTGGATAATAGAAGGTTTGTGCTCCGCTCCAGCGGTTCGAAGGAATACTGTTCATATGTACGCTGATAAACAGATCGGCGCCCTTCTCCTCGATGCTTCTGACCCGCTGCTTCAGATCCTCCGTCTTGCGCTTGGCATACCCTTTGGTGCTGTCCTGGGCCAGATCATAGTCGCCTTCCCGGGTCATCACTACGATCGCTCCCGCCTGCTGCAGATAGTCGCGCAAATAAAGGGACACCGAGAGGTTAATATCCTTCTCAATCAGGCCCTCACGGCTGACTGCACCGCCATCGGGCCCCCCGTGGCCCGCATCAATGGCAATAACCTTGCCTGAAAGCGGCAGACTCCAATAATTGATCGTCTTGGCAGTCGGCATATCATAAGCAATGATACCGATCATCACAGCGAGTAGTACAGCGCCCAGGATGCTTTTTTTGATGCTGTTCCAAGAGATCCAGACCGAGACTTTATGCTGCTGTCGGCCAGACATAACAAAGACCCCCTCGTCCCGATAGATTCTACTCATCTATATGGGACAAGAGGGCCAAATAGTACTGGCTGTTTAGGACTTTACAGAGACTTCCGGAGACATTCCCTCGATTAGAATCTGCGCCACTTCAGGACGCGTGAATTCAGGAGGAGGACATTGTCCGTCGCGAAGAAGTGCCCGTACCTTGGTACCGGAGAGCGTCAAATGCTGATCGCCCGGATGCGGGCAGGTTTTGCTCGAGGCCATATTGCCGCATTTCACACAGAAGAAGCTGTGCTCGAAGAATAATGGCGTAATGCCAAGCTCCTCGGCGGTAAAGTTCGCGAAGATCTCCTGCGCTTCGTAAGTGCCGTAGTAGTCACCCACACCGGCATGATCACGGCCGACAATGAAATGTGTACAGCCGTAATTCTTGCGCACCATCGCATGGAATATCGCCTCACGTGGTCCGGCATAACGCATTGCCGCCGGGAATACACCAAGGAACGTGCGGTTCTCCGGATAATAATTCTCCAGCAGCGCAAGATAACTCTTCATCCGCACATTGGCCGGCACATCGTCAGACTTGGTTTCACCCACAAGCGGATTCAGGAACAGAGCGTCTACAACCTCCATAGCGCACTTCTGGATGTACTCATGAGCACGGTGTACCGGATTGCGTGTCTGGAAGCCCACGACGGTTCTCCAGCCTTTATCCGCGAAGATCTGACGGGTCTCGGCAGGATCGAAATAGAACTCAGCGAATTTCTCAGGCTGCGGCCGGTTCAATACAGTTATAGGACCGCCTACATAAGTTGCCGGACGGCCGAGCAGTTTACTTACGCCAGGATGCTCAGGATCGGTTGTCTTAAAGACATTCTGCGCTTCAAGCTGCTGATCCACTTCGTAGATGCTTTCAATATCAAGCAGTCCGTAGACAATGCCGTCATCTTCACCAATCAGCGACACTCTATCACCTACTGCAAGGGATGCCGCCTGCTTGTCATCTACAGCAAGTGTGATAGGAATGCTCCATACGGTTCCATCTGCCAGACGCATGCTTGTGACCACAGATTGGTAGTCCGCTTCATTCAAGAAACCAGTGAGCGGCGAAAATGCCCCAACACCAATCAAATCCAAATCAGATAATGTCCATGTATTAAGAGCAATTGATTTATTGGCTGAGGCCTGCTGCAGCAGTTCTTCTCTCTGTTCTCCGGCGGCGTAGCGCTGGATCAGTGTTCCTCCATGAGGAAGTATTGAAGTCATTCCTGTTCTCTCCTCCTGTGTGCAATGCTAGTGTGTTATTTATGCAGTCCGCATTCTGTTTTGTCTGATCCAGCCCATCTTCCGGCACGCGGATCTTCACCAGGCATAACCGCCCGGGTGCATTGTTCACAGCCGATACTAGGGAAGTTACGGTCATGAAGCGGATTATATACCACATCATTCTCGCGGATATAATTCCATACATCCTCTGTCGTCCAGTTAGCAATCGGATTAAACTTCACGAGTCCGAATTTATTATCATACTCTACCTTCTTGGCGTTAGCCCGGGTAGGCGCCTGATCACGGCGGATCCCGGTAATCCAAGCGTCGTATTGTGAAAGAATACGCGTGAGCGGCTCAACCTTACGGATGGCGCAGCATTGATTCGGGTCAGTGTTCCATAGTGCCTCACCATACTGCAGTGCCTGCTCTTCCACTGTAATCTGCGGCGATACACGGACGAATTCCATTCCGTACTTGCCAGCCATAACATCTCTTGTCTCATAGGTTTCCTTGAAATGATAATCGGTGTCGAGATAGAACACATCTGTCGATGGGCTGACCTTCTGGATCATATCTACCAGTACTACATCCTCAGCACCAAAACTGCAGGCAAACGTTATATTAGGAAAAGTCTCTACCGCCCAGCGGATAATCTCTTGGGGAGTGGCATTCTCCAATTCTTCAGCTTTAACTTTGATTAAATCCTCTTTCTCGAGCAGATTCATCTAATCTTCCTCCATCCGGATATAGCCAAGATCGAATCCTCTGAGAGATTAATCCCGACTAATTCTATATGGTATAGTATATCCGTTTCAGTGGCGAAGTCAATGGGTTTTGTTCATTTTGGAATAAAGTATGCGGGGAATTAATATTTGGGTGATAAAAAACATATAAAAAGCTCCCGGCCATAAGGCTGAGAGCATGAATTCCTTTAGAACAAGGGAATAGATATTATTTAATTGTTAGTTACTGCTTGTGTAAACATTTCAAAATGTTGTTCTTCAGTGTACTCATTTGTTATGCGGCCCTCTGAGGTAAAGGAAAGTCCATCATGACGTGTATATATCAACAAGTTATCTTGAACCTTTGTATAAAATAATTCAAGGTTATATATGCTTTTTGTCTGCATCTCATTACCGTATTCAACTTCAGCTTTGCTTATAGATAAAGTTAAAACTTTCTTTCCCTCATAGGGACCATAAATTACTGAAACATTAGATTCGGTATTTACATTTTTAATAAGTTTTCCTTTCTCGTCAGTATACGTAATCACGACAGTATTCCGGAGACCTTCTTTCGTCTCTTTATCAAGATTGACAAAGATTGATTCTACTTCCAATCCAGGAATGGCTGGTACTTTTGCAGTATCTATATATTCTTTTATAGTGTCATTAGTTTTGGTGAAATTTTGTTGATCTGAAGAACACCCTATGATCGTAATCAGTAATAAAATAACCAGCATTAATTTTCCGGTTTTCATGGTTCCTCCTTCATTAATTAGATAGCAGGACCTTAGGTGAGATATCAATAACATACCACTATTTTACATTATTTACAAAGTGTAAGATGACTCTTAACATTTCGAGAACTGTGGAGCACGACGAGCGCTCTTAGGCATGTTTCTTACGTTCAGGCAGGGCATAGCTGCGCTCAATCAGTGCCACCGTAGCTGTTGCAAGTACCGGATGCAGCCCATTAAGCCGGGACAAGGATTTAAGCTGTACCTGATCAAGCGTCAGCATCGCGCTTCGCCTCCTCTTTAACGGCCGGAAAGATCATAAACAGATCCTGCCGCCGGGTATACATGAGGACAGTCAGGATTACCAGCCCCAGCGTGGTACCGGTCTGCGCAATAGCCCAGCCTTGTGATTTCAGTGCGGCATAAACAGCGGAATCCCCAGATGTGATTGAGAAACGAATCCAGAATGCCACGGCCATCTTGACCGTATATGCCCCCAGGAAGAAGAACGCAGCCAACATGAACAAGCTCACCACCCGGGCGCGGAATCTCTTCCGGAAGTACAAAAAAAGCGCGGCCATAAGCAGCAGCGCACAGATAAATGATATAAAATAAGCAATCAACAGCAAAATATCAATGCCCCCCATGATTAACACCCCGATCGTATATTAGAAATTCAGCAAAACCGTTGTTCCGGATCTCCTCTTGTATGTCCTTTGATGTATCCTTGTACCTGGCAATCGCAAATGATACCCTGCGGGATGCCCGCGCCAGCTCCTGCTCTCTCTCTTTATGCTGGGGCGATAAACGTTTTATCCATCGACTAAACACGGTTATCCTCCCCTGTCCTCATCATTGCCGGCATTATTGCTTGCGGCATGATCTATTTTGAGCCCCTGAAGTACTTGGAGTGTCGGTGCCATAAAGTCTGACCGCTCCTTGTCGAGGATACTTTGCAGCCGGTCCCGGTCCTCCTCGGCACGATCCAGCAGCTCACGCGGCACCCATTTTCCGCGCCGGATGTCTCTCACAAAGCCAAATACTACGAAGACCAATACAAGTGCCAAAATGTAAGCAAGTCCATATTTATCTGCGAGCGGCAGCAGCTTTTCCAAGTTCAATACATTGTTGTTATCCATTCCCCCGCTCCTCTCTCTGATATAAAAAGCCCCCGAAGGGGCTTCGGAGGCAAAATAAAAACGCCATTATGGGCGCTAGCGATATCTATTCAACAGGCAATGGGTTCCGATCTCATCCAGTTCAGAAGCGGCCCAGCTAAACACTAGTTAAGCATTGTCGGCCAGGAGTGCCTGAACCTCATCTCGGATCACGAGGGGGACCTGCTCAATTGTTTTGAGTCCCTTACGGATCAGGCTTGCATATACTTGCGGCATTATACGTCACCCCCGATCAGCGGTAATACTAGCTCGTACAGTTCAACCAGGGCAAGCTGTGCGCCTGTGGCCTCATCTTGAGCAGACTGTAATTGCTCATACGTCTTCGTCAATGCTATCCGAGTTTGTGCCAACTCTTCGCGTACCTGCTCAATTTCCGTTAGCTCCGGTGGCTTATTGGCTTCGGCCTCCTGGTAGGCTTCCCAGGCTGCTTGCAGCTCAGCTTTTGTAGGTTGTGGTTCGTCTAAATTCCAGAGCGCGATATATGGGCCACGCTCTACCAGGTCGTAATCTTCGCCCTCGGTCAGCAGGTTATAGTCGATGCCGTAACGGTAATGTATGCCCTCAATGGGTTCCTCGCCCTCTTCAGGCGGCTTAATCTCATAGCGGACCCGGCCTTTTTCTTCGGCACCGGGTCGCAGAACGGGTTCCGGGCCGTTATTCTGCACCCTAAAATCTCGCATTGGGTCAGCGTTCGGGTATAGATACATGATTGCCAGTGCTATGTTCATTTTTCAAACCTCCTTCTATGTTCTAGGCAATTCTCGTAATCATGACATAAGAGTAAGCACCATCCGGGTTAGTTGTTGCACCTGCAGTGCTAGTCATCCAAATAGCCAGCGTGCCACCTGCAGCCACCCCCAACATCAATGCTCCACTAGCGGCAGTATAGCCAGAACTTCCGGGCCGTGTATGAGAAATAACTGATGTAACCCCGGAGCTTGAACCTACTGCTAGTTTCAATTCAGCCCCGCCCGTGGCATTAGTGAACTGAATTGAGGCTGTAATCGCGTACACACCCGCCATTTTAGCGGTAAAGACGCCCGTTGTCGGATCATACTCTCCTAGATTGTCGTTACCTTCCGATCCATAAATAACCTTTGTCCAAACGTTCGTGGCTATGGTTTGTTGAGCATTATGAGTGCCGTAGATAAATGATCGTGCCGACCATGTATTATCTCCCCATGGGTTAATAACTCCACCATTTGCCCCATCAAGGGCACCACTCATTATAGTTCCCGAAGTGTTAACGAGCGCCCCGCCACTTGGAAGAATAGCCGTGGTGTTTCCGGTTCCTGCGCAATTTATAACGGTTACTTGCCCCTTCTCCACATGAATTGCAACACTGCGATTAGATATTGTACACCCTTCGACTAATCCACATTGATTAAAGAAGGTAATTCCTGTGTTAGCGCTAGAAGCATTCACTATACAGCTAGTAAAATCGCACTTCCCACCATCATACGCATAAAATGGCGACTGAGTGGTAGAGGTTGCTGTAAAACCATTAACTACAACACGAATACATCTCGCGGCGGTGAATGATCGAATAGACGCCGAAGTGCCATTAAACGCAACATAACCCGCACCATTAGTCCCGGATATAATCACATCTTCTGCATAAGTCCCAGCCGCAACGTTGACAGCAACCGTGTGATTAACCACCTGCGGAATCATGCTAATCGCTTTGCCGATCGTCTTGAACGCCCCACCCGCAGTATTAGCCAGCCCTGTATTCCCATCATTACCATCCGTCCGCACATAGTAAGTAATATCCGCCGTGGTCTGCTGCGGTGTAGCGGTTAGATTGGCCTTAGTATTCAGCTGCCCTTGAATCCCCGCTGTCACGCCGTCCAGGTAACCAAACTCTGCATTGGACACAACACCTGTCCCGATCTTGGTAGCATCAATAGCTGCTGCGGTATTAACGTCAGCATTAACAATCGCCCCTGCGGTGATTGTAGCCGTCCCCGCTCCTGCAGCCATCGTGATATCTCCGGAGATAGCCGGGAGACGCGCGGCGGCAAGCGTTCCGCTCGACAAGTCCGCAGCGGATCGTGTAGGCAAGTCCGCCAAGGATGCCCCTGTTTTGCTGAGCTTGCTCCAGGCAATGGCTGCAGCGGCATTTACATCCGCATCCACAATTACACCGGCTGCAATCGCAGTCACACCGTCCCCTGTACTGGTTACATCACCTGTATGATTAGGGTGGGTGTATACCGTGGCATTCGTGCCATTGATGGTGATTACTCCGTTTGAGGCCGAATTGGCTACAACAGTAGCCCCGGCTGCAATGCCGTCCAGCTTGGCTTTATCTGCGGCCGACTCCAGTCCGGCAGTTGTCGTAGTTGCTACAGCGGTTGAGGCTTTAGCATTCCAGGTTGATTTTTCAGTATCGGTGACGAATCTATTCGAAGCATCTTGCACAATGATGCCTGGTGGATGTGTGGCTGGGTGAGTATAGTTATTGGCTCCTGCTGCTACTCCATCCAGTTTCGCCTTATCGGCAGCCGATTGAAATCCGGCTACTGTTGTTGTAGCCACTGCGTGCGCCGCGCCTCCAGAACCAATATGAGAGGTTAAATTAGCCTGGACGGCATTAGCCTTAGCCGTAGCATCCGTCGCAGCCGCTGCCTGAGCAGCGGCCGCTTTTGTGGTTGCGTCAGCTGCCGCTGCGGTCTTGGCAGCATCCGCCTTGTCCTGTGCTCCCGCCGGTGTCTCCTTAGCGTTCCATGCCGTCCGCTCCGCCGCCGTAAGATGCCGCGTGGCATCATCCGCATGCGCCTTAGCCGCTTCCAGCGTTGTGGCCGGCGCAGTCCGCCAAGAAGACTTGCCTGTGATAGATTTGATCATATTGGCCAGCCAGCCCAGCAGGGTTGTAATAGTGCCAGAATCTCCTGTCGGGGCTGTGGCATCTGATATTGTCCGGTTGCCTATAACCGCGTCTGATGCAGACGCGGCTCCGCCAGCCCCCGCCGTAATTCCCGAGAGTTTGTTCTTCTCGGTCGTGGTGTAGTCATTGGCGGACAGCCCCTTGCCAGATACCTTATCTACCTTAGCAGCGTCAACAGCGTCCAACTCGGACTTTTTCGCGAATACTAGTGATTCATCAATCACCGCCTTAATATTCGCCGCCGTCCCAACGACAACAACGCAGTCAAATGCCTTCTCAATGATATCCGTTCCGCCGCCGGGCGCGATATAATCCGCTGTCACTCCGGCATTGGCATAGGCGTACAGGATCTCTCCGCCATCCGGATCTTGAGCAAATACCCCAACCTCCCGGAAATAAAAGCCTGTGGTGATATCGGCGTTGGACAGAGTCGTGCCGATAATCACTTTGTTAGGCGGTTGCATCTGAAGACGGGCAATAGGCAAACTTTTCTTGAGGGATATCAGCGCATTTAGCGCTGGTACGGATTGTCCGCTAAGCGATCCGTCGCCAATGGCGATCCTGGTATAGTTGAGCTGTGCTCCCGCCTGTGCTTTTCCTTGCAGTGCCAATCCTTTATTGGTTAATGTCATGCCTCCAAATACTGCCACATGTTTCCCTCCCTAAATCGTAATGTGTTCCCCGAAATGTAAAAAGCCGCCGAAGTAAAAGGGCAGCTGCTCAGCTTGTGAAATTGTGACGCTGTCCAGCACAGCTGATAAACGTTTGACTGCATCGACAGCGGCAATGAACTCCTGTGCCCGCTCCGCAGTCACATCGGCATTGTTGGTGACTACCCGGAAATGATGCGGATCCCCGCCATACTGCCACCATTCTTCCACTGCACCTTGGCCAAACAAGATCGCAATCAGGTCCTCTACCGCTCCGGCTGTACCTTTATGCCTGTGAAATGGGATTGCATTTTGGATCAGCAGCCGCTTTTGATCCAAAGGCAGATCGGGATCATAATAGGGCGGCTTGAACTGCCAGGCCAGTTCATCTGCTTCTGCATTAGTCCACTCTGCTGACCGCCCGAACAGCTCCAGGCCAGCAATCATTCTGCTTGTCTCTTGCAGCTGTATATCCAGTGCAACAGCAGCCGCAGCCATAGCAGGATCATTACGGATGGGAAGCGGCAGCAGATCAAACAGACTTACGGTCTGAATATTAATCATCTGCCAGCCCTCCATAAGTAATTGTCGTTGTGCCAGTCTGAGCGATCTGGGTTGCTGACAAAACCGTGTACCCGGGCGCTGCCGCGACCACCCGTAGCGCCCCGGCGGCCATGATTCGGGCTATCAACTCCGAGGGGTTAATATCCCGTCCCAGCTTGGAACGCTGCCAGAGCTGATAAGCAGCAACTGCCGCCGATACGGCTGCCTGGATACCAGGTACCTCAGCAGCCCGGCTGCGGCTGATATAATAGGTAACTGCTGTGTTAAAGCTGACTGGTTGTGGCGCACTCACGGTTACCAGGTCTGTCAGTGGCCGGATCCCCCGGTCTTCCAAGGTCTCGGCAATGGAACTCAGCACATCTTCACCGGGTATCTGCCCCTCGGCAAGTAAAGGGACGACCGTAACACGGCCTGCTGCCGGAGAGTACGCATGAACATCCAGGATCGCAGAGGATGTGGACTTGGCCCAGAATTCGTAAGCTCCCTGTGGACCAGCCGTCGAATAGGATTCCGGTGCGTTGCGGATACGTTCTTTGAAAGCTTCATCCGTTTCTGCAGCGGCTCCACCGGAGCTGGTTGTCAGATTGGTTACAGATTGGACAAAGGGCAACGGGTCCATCTGAACGTTAATCTGCCCGGGTAAGAATCCGTTCCCTATCGTTCCGGAGTCGGAGCATTGTGCCGTTGCAATACCCGCCGTCTCTCCCGCCGGAATTTCCAAATACTCCGTAGTTGTAAAATAGATTGAACCATTGCCGCCCTGCGCCCCAACGCGGGTTCCTGCAGGAATCGAAGTCACTGAAGCCAGCGGAATGGATAAAACAAACTGAAGAGTGACGATTGCCGCCGACGCCTTCAAGCGCTTCGAACCCTGAAAAACGCCCATATGATCCAGGAGCGTCCCGGAGGCGTAGCGCAGCAGATTTGCTTTTGACGTCTGATTAATAAGCACCTTCTGCTGTACAATGACCGCTGCCAGCGAGGACAAAAAAAGCCGCACCGGATCGGCGGGCTGCAAAGTGCGTCCAGCAAGGCCTTCATATATAGTGATCACATTCTGCTGTATGGCTGCTGCGTCCTCTTCGACGAAGAGAATTTCCGGTAATTCAGCATATTCCAACGTCTATTCCTCCTCTGCCAGAGTATATTTCACTACAACTGCCAAACGGCCGTTAAGCGAGTTTTCTTTATCTTTGTGAAAAGAAACATCGGCTACCGAGGCGCGCGGTTCCTGTTCTGTAATGGCTGTGATGATTTCTGCGGTCAGGCGGGTTTCGGCAATGAATGCAGGCTCATCAATAATCGTGTAATCCAGGCCAACCTCCCGGACCAACGGAGCGCTTCCCCACGGAGTAGCTAGGATCATCCGAATATTCTGAGAGACTTCTTCCTCAACCGTTAACGGACTGAAATTGATCAGGGTGGGCTGTGTCATATCCACGGTATACATCATTTCACATACTCCTCAAGTGAGATTGTGACCTGTGCGTCCAAAACATTGCCGATGCTATCCAGCCTGCTCCAATCCTGGGACAACCCGCTGATCACCCACAGTCCGACTCCCACATTCTTACGTCCTATGACAAGCGGCATCGCTTTACCGGCACGATCGAGTTCTGTGAGCCTATCGAGTTCTTTACGCGGATTAAGGCCAAGCGCAGCGGAGAAATGGACCGCAAACGAAACAGAATCTGCCCCGGGTCCCACAAATTCCTTTTTGGGCTTTTGACCGATAATGTCGTGCTGTGCCCACCGGCTGGAGCTGCTCCGCTTGAATTCATCTATAGTGCGAATTGCACCTTCCGCAACGACAAAAACGACCGGCCCTAAACTGCCAATCTTGTTCATTTTATATTCTTGTGTTTGGTCTGACTTAGCTATACTGCTCATCCTGTTCCACCACCCCACCATCATTAAATACGCTGGCCGACACCTTGCCTGTTACTGTTAAATCTCCCTCGATCCTCACCCCGCCGCTACCTTTAACATTCAGTCTTTTGGCCGTACGGTCATAATAGACATAACTGCCATCCTCAAACCATACCCCCCGCTGATCCTTGCTGCCTGAAGGCTGATCGTCTTCTGCAAAGTACGTTCCCAAGCAAAAACCTGCCGAACGCCCGTTATCCAGAAAAACGCACAGCACCCTCTCGCCCGGCAGCGGTATCGCATTGCCCCTTCCCCAACCGCCCGGCGTGAGAACCGGCAATTCGCCAGAAACCATATCATCGCGGTCTGCAAAAGAAACCCTGACACTTCCCGCTGCCACATTAACTGTGGATACCCTGCCAATAAGAATCAATTCTACCACCCCAATACTTTGCGAATTTCCAGATTTGTTGTGTACCCGTTGCTTCCAATCGAATGCCTGGCGGATTCTATGATGTATTTCCCGTCAAACCGCTGCCAGCCCTTGATATTAATGGTTAGTCCCGTAGCCATCCGCATATCACCCATTAGGGAAAGCGTCCCTCTTCCGCCTTCTTTATTGCGTTCCCGAAGCCTTTTGCGGGCTAGACGCAATGCATCAGCCTGGCTATCGACTTGCTCATTGATCTTAAGCACAGGACCACTCTTCGGCGCACCCTCAGGTGTGTAAGTAGCCTTTAGGGGCTCTTTGCCCTGGGGAGGCGTATACGTAACCGTACAGGCCCGGAAAGCCGCATATGCAGTATTTAGCGCAAAGCTGTACCCTGTCACATTAGCCTCCCCGCGCACAATCGTCGCGACCGCTGCTTTTTGTTCATATTCCCTTTCATCAAAAAGAACCACACTCCCGCCGGATACTTTAATGGCGATGCCCTCTTGAGTAGCTGTGTTCAGCAAAAAGGCCAAGTCCGACATCTCCGACTGCTCCAGACGTTCATAAGAAGGATTGTCCTGTGCCTCATAAATTAGTTTCAGTTTAGCGCGTTTGGCAACTTGAGCGGCTACCGTTTTCAGATTGGTTTTCTCCCAGCTGCGCGAACTGCGTTGCATCCGAATCTCGGAGGTGATGGGAAGTGAAACCGCCTTAATGGATATCGTGTCAGGGGGACCGTTAAAATCAATACTGTCCACCTCAAAGGTTCCCAGCGGCAGCTTCTTGATCTCACCCGGCTTCCCCCAGTTGACAGTCCGGATGGAAGCAACCAGCTGATCTCCTTCAACAGGTGCCCAAGGTCCCTGCCAATTGCGATCCCGGTCCTCCAGCGAAACTGTAAGATCGTCCAGAGAACCGGAGGCAGCATCGTTATATTGAAAGTCAGTTAGCGATTTCGCAATATCCACCGTGACATCCTTCCCGTTATACCGAAGCTCCAGTACTGCTCTGCGTGCGTCCTGCATGGATTCCATCCGGCTCACCCCCTTCTCCATGGAGGTAATGAGCTGGAGGTGTCAGCCGGCAACTCCGGTACATTCAGCACAATATTGCTGGAAAACACACTGACCGGAGCATGTGCTGGATTAGCATTCAGGAGCAGAGCCATGAATTGGGCGTCACCATATAGTTTAAAAGCTATTCCATCCCACATATCTCCCTGCACGGTTCTATAGATCATTGGAAGCTCACCCGCCTCTGCTGCTGGAGCATGGCCTTGAAGCGGCGTTCAAAACCGTCCTCCGTTTGTTTCAAGGCCTCACGCAGCTGTTCGACCACAGATTTATCCCCGCCCTGGAGGGTGATACTTGGGGCCCACGTTACATGAATATCTCCATTGTTACCGGAATTGTTATTGTAGCCCATCAAATCATTTGCCTTTTCCAATAAAGATCGGGACCGTGGCTTCTGATTTAATGGAATGGCCATTTCGGGACCGGCTTCACCAAATATAGATGGAACATATGCGATTCCGCCTTCAGCGTATTCCGCAATTTTTGGACCACCATAGAGCGGCAAATATGGCTTTCCTTTCGAATTGGCCGTTTTTCGCCCCTCATCTCCCGCAACATTGAAATTTGAAACCTCTCCGATCTGCTGCCATAGGACCTGAACATTCACTATCTTTTCAGCAGGCAGTTTATCCACCTCATTATTAAGGCTTGCCGTATCAATCAATGCTTGAGTGATCTGTTCTTTTTGAGCAATGGACAAATCCTTGTATTTCGCTACTTGCTCTTCTAAGGTGCCCCCAAGATCAAGCTCAATCAATTTTTTTTGGGCATTGTAATAAGAGAGCATGCTGCTTTCAGCTTCTTTTTTATCACTTTCGGTCTCTTTGATTTCAGTGTACTGGTCATCAAAGGAAGTCCTATACTTTTCGTAATCTTGTTTGATCGACTCAATAGCCCAACCGCCGGAAACATCGTATTCTGTACCCTGAGCTTTATTGATTTTATCTCTTAATGCATCTATTTGTACTACTTTCTCCTTTTCGCTTCCCTTTCCATTCCAAATCTCATCAAGCTGATTCACGTATTGGCGATAATCTTGAAATTTCGCCATATTAGTATCATATTTAGCGTACTGCTCGGCGAGTTTCTCAGTCGATGCTGTATATTCATCCTCCAAATCAGGTAATTTCGCCTGAGCTGAAAGTACATCATGCTCTAATTCTCGCCGGCTCATGTCCTCCTGCGCTTTGGCAAGATTCCCGACAAGTCCAAGCTGATCGCTGAATCTGCCACTTTTTAAGTCTTCCGCAGACAGAATATCCGGATTCATGTCAATAAGCTCTTGTTCCACAAGCTTCTGCTTTCGCCTGGCTTCTGCCAATTCAGCAGCAGGAGTTTTGGCGTCCTTAAGCTTCCCTGTCAACCGGTCATACTCGGTAATTAGACCCTGGGTTTTTGCAGTCGTCTCCTCAATTCCGGCATAATTGGAATAGGATTCATCCAGCGCATCCCCCATATTCAAAAGCTCCAGGCGCGCATCCTCCTGATGCTTTCTGAAGGCTATGACTCCTGCAGCGGCCAACCCTATACCCGCTACGGTGAGACCCAACGGATTCGTGAGCATACCCAGCGCCCCGGCAATTCCTCCAGCTGCTCCGCTGGCTCCTCTGGCCGCCGTGATAATCTTGGAGAATTCCTGGACAATCTTGACTGTTTTTGTAGCCAGCATCGCAGCAGGAACCGCAAGACCGATTACCATCAGCGGCTCTTTGTTGTCTGAAACCCAGCCTGTTAAGCCCTGAAGCGCGGGCATCAAGTTTTCTCCCATGGGAACTACAAGACTTGCCATCAGCTCCCGTCCCATTGCCGCAAACTGCTCTGAGAGTGTATTGTCTTTTATCGCCGCTACTTCCTCCATGGTCTGCCTGGTCATATCAAACTGATTGCGGGTTTGGCCAAGCGCCAGCACTGCCTTGTTCCCTATTTCCTCAAATTGAGAGCCGAACAGAGTACCGGCAAGCGCTGCTTGATGAACCGGATCCTTGATGGCCTTCAGTTTCACAATAACCTGATTCATTGCATCCTTACTGGTAATCGATCCGTCTGCCAACCCTTTAAAGAGGCTATCGCCGCCGCCGAGCGTCTTTTGCAGTTGAAGCATAGCCTTTTTGGCCGAATCTCCTCCCGCCTTCAAGTCTCCAACCAGTGCAAGGGCACCCTTTTGTCCGGCGGCTTTTACCAAATCGGCAAATTCCTTCGACTTCGTCCCGCCACTGACAAGCGCGGCGCTGAATTGATCCAGCTGCTTAGGAGCAAACAGCTCGTAGACGGCGGCCTTTGCAGTATCCGAGCCTGCTTTAACGTTTGATCCAAATTTTTTCACAATGTCGGCAACACCATCAAGCGAGTCCGCTCCGTTGTCCATGCCTGCACTTAATAATTCAAACATCTCGTCGGCAGAATAACCCATCTTCTGAAAATCATCGCTGTATTTCCCTATTGCACTCAAAAGTCCGCCGGATGTGTTCAGCCCCTTCTGCGCGCCTTGAGCCATCAGATTATAGGCTTGTTCCGAGGAGATGCCGAATTTGCGCATCATAGCGTCAACTGCTTGTACAGAGCCAGCTATATCTCCCTTAAAAACATCACGATACGTCATAGCCGTCTGCGTTGTCTTCTCCAGCTCTTCTCCTGTTTGCTGCAGAATTTGTTTCACTGTTCCTACGGCGTCACCGATATCTTCATAGTTCTCACCATAATTCTGGCTGTACAGGTTATTAGAGATATCTTTCATTCCACTCATTTCTTTGGCGGTCAACCCGGTTGCAGCCTGAAGCTGCGCCATCGCCCCGGAAGAATCATTTACAGCCGCCCATACCGCCTTCAGAGGTTCAACGGCTTTTTGCAGCATGGAGAAGTCCACTTCTTTGACTGCATCTTTAAGCTTGTCACCGAGTTTTCCGGCCTTGTCGCCTACCTCCTCAATGCTGTCATCCGCCTGATCAGCCTCTCTCCGCAGTACATCGAAATACCCCCTGCTGACCATTTCCTGCAGAACCCGGTCCAAATCCTGAATATGATGTTCCGCTTCCCCGACAGAACGTTGGAAAGCAGGAGTCACCAATAAATTCAGCTGAAGAATAATCTCATTAATGCTGCCGCTTGAATTGCCTGTCCCTGCCATAAGTTACCTCCTTCCCTTAATCCTGGACACCCTCTCTACCCAATCCCCCAGTTCCTCCAAAGGCAAAGCGAGAAAATAAGGGATGGGAGTATGGGTGAGCATGGCCAAAGAGACGGCGATGTCTTTAATCCCATCGCCATCTCCGCAGCCTACAGCAGCAAAAAACTTTGTGCCCGCAAGGTCAGTTTTGTAAAATCCTTAGCTGAAAGTGCTCTGATCAGCCCAACGTGGACACCTGCAGCCTTTGCTACAATATAAGCCTGATAGGCTTTATTGGTCTCCTTAATCAATTCCCCGCTGGATTGCCGCGCCGACTCTACCTGATACTGCCGGTCACAGATCAGAATGTCTTCACCTGTCAGCTTGTCGAAATCAATACTCAAGCTCTCAAAAGTATCGCCTTCAAATGTTACAGGCCGGGCGAAAGTATAGACTTCCGCGCCAGCCTCCTCTATATTCTTTGTCCCCATCGTGCACGCTCCTTATAGACTAAGATTCTCTTTGGTTGCAGCAAGGTAATCTACATCATAAACTTTGTGAATGTAGTTATATTTATCAATTTCCAGCACCTGAACGCCATCCAGTGTCACCTTCAAATAATTCACTGAAAAGTTGTTGGTGGTATCCATCACTGCGGCAGTCTCGAGATTCCCCAGCGTTAAGCCAAGCGGTCTTGCACGGACAGTAACCTTAAAAGGCACCTCACGGTATTCACTTGTTGCCGTGTCAAAGGTTTGGATCGAAGCCCGGAGATCCAGCGTATGGATCTTCGGTGCCAGAAGCGATGCCGCTGCCTTTTCAATGGTGCGCCACTTGAGGGCCAGACTCATCGCTCCCGTGTGTCCCGGAGAAGGCGCCGCCATTTCTCCGGCGATTCCGCCGCCTTTAATTGTATCCACCAGGTAGGTGATTTCCGGCAATGTGGCGGTTGCCGTACCCAAATAATCCACTGCATTCAAGTACACCGAATAATCAATAACTCTTTCTGATCTTTTAGGCATATTGCTCCTCCTTTTACGCTACCAGCGCAGCTAAGTATGTTGTGTCGTATTCAAGCAGGAATGAAATCTCCTGTGCCGGTCCCGGCGGTGTGATGTGCAGATGGAAGGTAACCTTGCCGGCCATCAGATCCGCCACTGGATTCTCGGACTCATTGAAGTCTACCCGTCCGCCCAGCAGAGCTCCGGATGCCGTCAGACCGTTCAGCCAAATATTCACTGAATCTGTGACTGCAGCCACCAGCCGCTTGTTCATCGGATCATCCACCTTTTGCATGTAGGTCAGAATCAGACTGTTGCCGATCCAGTTAAACATGCGGCGGACCGGAATAAAGCTGTCTTTGGGGTCAGTGGCACCAGGGTAGGCAGCAGTATGATTCCCCCAGCTCTTCCAGCCGCTCGTCCCAAGATTAAGTGCCGTTACAATTCCTGCGCTGTTAAGGAAGCTTGCCTGGTCTATCCCCAGGAACTGGCTTGTCCCATCGGATAGTACAGTCCCATCCGCCTGCAAAGATTTATTAGACGGCGATACAAAAGGAACACCGCCATTATTGGCATCTGTCGCAGCGATAAGTCCAGCGAGCTGTGTAGAGAAATGATATTTCTTATCCCCTAGAGTCAGCATCGGGTAAGCCGCAACTTGAAGAGGAGCAGTGTAGCTGTTATCCGCTTTCCATGTGCCAGCATCTGTATAGGACTGGGACGGATCAATGTCCGTCAGCGCCATCGCCTTGAAATTCCCGTTGATATTTCCGGCTTTTGCCTTCATCACCGCAGCGACTGCAGACAGATGTGACCAGCCGGGAGCAAGCAGCAGATCCGGAAGAATGCCAAAACGCGGGTAAGCTTGATGGACCAGTTCAAAACCGGTATATTCTCCGGACGGGGTCACGCCCCCAATGATATCCTCAGCCTCTACAGCTTCCGGATTCAGCTTGTCATAACCCACGGACAGTTGATTAACATTGGCCGCGATAGCACCAGACGGCTTTGTTGAGATCATCACATGACCGTTCTCATCAAATGCAGCCGTATAATCCTTGCCGGATACATAGGTTGATGTACCGTCTGAAGATTTGACAAGGAGTGTGGACAACAGCACCCCTTCCGCCTGCAGGATGGCATCCCGGTTAGTTACAGCAGCCGCTGTTGGAGCAACCGTTGTCTTGTGTGTGGCCGGATCAAGCACGTTGACCAGAATCATTGGAGCTTTTTCATATAACGCAAAATGTGAATAGATTAATTCGCTCAGTGTATATTTTGACCAGTCCTCGCTGTACCCGAAGGCAGCCACCGCTTCCGCGTAACTATATACAAGTACCGGAGTATTCACCGGCACAGATGCCGCAGCCAAATGAACCGGAGCCGTTCCTACCGCAAAAGGAATACCGCTTGTTGCCTTTGTTGGAGCCAGAACTGAAGTCGATTGTTCAATAATAGTTACACCATGTTTAAAAGCCATATATTAAATCCCCTTCCCTAAAAGCCTTTGATAGACTGCATATTCAGCTGTTCCTGCTTGAACAATACGTTCCTGCACAGCCGTTATTTCTTCTAACGGTATAATCAGTTCAGCCACATCCGGCTGTTCCTCCAGCAGCGGCAGTAGATAGGATGGAATGCCCTCCCGAAAAACGGTGGATTGCAGCAGCCGCCCGCCACGCAGATTTGGACCTAAATAGATTTGTGGCGGCTCCTGTGCCGGCTCCTGCTCATTTTGGAGATTATCTTTATTATTAATGAAGTTCATATTTGTACCTCCGGTCTAATTTGGGGCAATACCCAGGTTGTTGTAAGTTCGCCTCCCCAGTCTGCTGCTGGGTGCTCCTCGTTAAGTTTCATCTTCCAGCTGGCGTCCATGACGAATTTTTGTTCAAGTACTCTCTTGCGCAAAAGCAGAATGCGTACCCGCTCCATCAGATTAAGCATATCAATGAGTCCTGTGTCATCTTCTGACTGGGCTCCAAACTGTAGTTTAATTTGAATTTGCCCTTGACCAGAATCACCTTCTCCTTCGGCCGGCCTAATCTTAATTACCGGATATCCCGGGTTCCCGGCATCACTCTGCGGCAAATATCCCAGCAGTACGGATGGTACGGGCAGCATGTCATCTGCCAATTGCTCTTTCAGATACTTTTGAATCGCCATGATTAGTAAAGTAATTGTCACTGTGTCCCTCCTTGCTCCTAGAACTCTTTCTCGAAGATACGGATCGTCCCCAACCGCTTCACCATCTTTGCAGTCACCTCCCCTTGCGGCATCAGCAGGATGAGTGCCGTTATTTGTCTTTCTATTTATTAGGGGCTTTCACTAGACAAAACCAAACATTTTATTTATATCCTCTTTAAATGAGGGACCTATACTCATCTATAACGGAGCTGATCTTTTTTTGCGCCCGCTGTATATATTCACTTACACTGCCAGCCGAAATCTGGAGCATATCAGCGATAGCCACATGCGAGAACCCCTCACCGTTAGCAAGCATATAACACTCCTTCTCCCTCCTGCTCAACAGCCCCAATACATATTCCAATTGAAAACGTTGATCCTCTGTGAGTCCTTCAGAAGGGACCGCATTGAAGTGACAGGTGAAGTTTTGCATAAGAATAGGTTCCAAAAGAATTTCCCGCTCATAACCCGCACGCCGTTCGATTCCCCGCTTGTTGCCCGGCCGCCGTCCACTGCTCAGCCACTCAATAACATATTCGCAGTCACTGACCATTCCGGCGATTACCTTTTTGTCTTCCGCCTCCGCACTTCTGTAAAGTTGTTCTACACCCTTTAATGAAATTTGATATTCTGGAATCAGTTTTTGCACAAATTCAGAATATATAAATTCCAGATCCACCTGCTCTACACACTCCATGTCAATTCCCCTTTCACCCATGTTGATTGAAATATACTCAATTTCGTATTTTTAAATCATGTTATACTCAATATCGCACTTAGTCAAGCTTTAAAACCTTAAAAGTACGAAAATGCATATTTACTTTTGCCTACAAACCTTCTACAATGAATTTAATAATACGAAGTAGCGTATATACTGATGATTTTGAGGAGGACTACATGTGCAACGGGCTGAAGTCTTAAAGAGGCTAATCGAGGAAACAGGCCTGAACACGAAGGCTTTTTCAGAAAAAGCAGGAATTCCTTATACTACGCTTAGATCAATCTTGATGCGGGGGGTAGGAGGAGCTTCTGTCGATAATGTTCTTAAAGTTTGTCGGGCTTTAGGCATTACTACCGAAGAAATGGATCGTTTGGCCTTCGGATCAAGTAAAGAAGAGGCTGCTCCACTGCTTTCGGAACTGTCTGAATTTGAGGCTTTTTTAAATAATCCGGAGCATGGACTGTTTTTCAAGGATTACCTGGACGCCCCGGACGAACGTAAACGGGAAATGTTGACCTTTTGGCAATTTATTAAAGATCTCGAAAAGAAAAAATCAGACTCTTCGGACGACAACTAAAAGCAGAAATAATCGTGGTTTCAGCCAACGGGCTGATTCCTCATATCTATATATACGAACATATATTCTTATCTCGGAGGTTTTTTATGTTTATTCATTATAAAAAAACACATCTTGAGCATTTCGTGGAAAAGCTCTACATAAACCATTCTATTCTTAAGCCGGAAGACATCACGATACAGAGGCTTTCGACTGAATTGGATATCCATATTGATTATGCTCCTGTCCGGAGCCGGGCTTATGAATCCATAACGGGTATGCGCTTTGTATTATTGGACAACCGTATTACCCCAATGAAGCAACGGTTCGATTTTCTGCATGAGTTATGTCACATGCTGAGGCACGCCGGCAACCAAATGACGCTGCCCGTTCCATTTATCAAGGCACAGGAGGAGGATGCTGAGAAGTTTGTTCTTTATGCCACCATGCCCTTTTTCATGATCCAATCCTTTAGCTTATCAGGAGATTACAGTACCGCCATTCAGCAAATTTCAAATGTTTTTGGGGTATCCAGGGAAATGGCAAAAGTACGCTTCGATCAAATTTTACGCCGTGAGTACGAGGGAGAGATGTTGCCGTGGAGGAGAGGAGAATATATTTCACATTCATTTGATCAAAAGAATTCGGAACCAAGTCATGCTTTAGATGAACCTGTAATCTTCGCTTACTACGATCCCCATAGCACACTGGATGGTCCGGATCAGCTTATTGTCTGTCTTGATCATGCAACATTGTCCACTCAGCATGAATGGATTGTCCCCATGGAGGAAAGGTTTAAGGAAATAGAGATAGATGCATTGAAGAATCTTGAACTTGAGTCTGCATCAAGAGGTGACTTAATCTGTTTTGATGGACAGCTTACCTTACAAATTCATCAGCTTGTGTATCGGCATGGATTATCTAAAAGGAATTTTGTATTGCAAATGAGGGATATTGAGCAGATTCTTGAAGCAGATCAAAGCACCGTACGAAGGTTTCTATGATAAAGAATTCCGCCAGTTATAACTACAAAAGCAAGCCCATGCAATTATGCATGGGCAATTTTTATATCCACCGGCAACTAAATACGCCCGCATGCGTAAAAAAGCTCCCGGCCATAAAGGCCAGGAGCTTGAGTTCCTTGATAACAAGGAGACAGATATTAACGTTTCGAGAACTGTGGAGCACGACGAGCGGCTTTGAGGCCGTATTTCTTACGTTCCTTCATACGTGGGTCACGAGTCAGGAAGCCGGCTTTCTTCAGCGCACCGCGATATTCAGGGTCTACTTTGAGCAATGCACGGGAGATCCCGTGACGGATTGCGCCAGCTTGACCGGAAATGCCGCCACCATGTGCAAGAACGATTACATCGTAGTTGCCCAGAGTTTCAGTCAGGTTCAAAGGTTGTCTTACGATCATCTTCAGTGTTTCTACACCGAAATATTCGTCCATCTCACGTTTGTTAATGACAATGCGTCCTTCACCCGGTACAAGGCGAACACGTGCTACCGAATGTTTACGACGACCTGTCCCATAGTATTGTACTTGTGCCATGAAACTGTCCTCCTCTATTCTTATCCGCGAAGTTCGTAAACTTCAGGTTTTTGTGCTGCATGTGGATGTTCAGCGCCTGCATATACTTTGAGTCTCAGTTTCATGTGATCCCCTTGACGAGTCTTAGGAATCATGCCGTGAACTGCGAATTCAATCATACGCTCAGGTTTGGTTTTGATCAGGTCTTCAGCAACAGTGACTTTCAAACCACCTGGGTGCATCGAGTGACGGTAGTATTTCTTGTTTTGCATTTTCTTACCGGTCAGGTGAATCTTCTCAGCGTTGATAACAATTACGAAATCTCCAGTATCAACATGTGGAGTGAATTGCGGTTTGTGTTTGCCACGGATTAGAGCAGCGGCTTCGCTTGCCAAACGGCCAAGTGTTTTGCCTTCGGCATCAATGATGTGCCAATTGCGTTCAACTTCGTTCGGCTTCGCCATATAGGTGGTACGCATGAATGTTTCCTCCTTGTTCTCGTACGAAAATCATCTGTTTCGTATATCTTGTTTCTCATTGGATTACAATTATGTGAGTTAAGAAAAGCTTGTTTGTTGGCATTTCCTTGATCGGGGCTGTGGGATAGCCATCAAGAAAACACAACTTTTATATTACAGCATAAACATGACAAGTGCAAGTGATTTTTAACTTTTCAAACACTATTTTTCATAAAAAATAATGCGCTGATCGTTTAGTTCTCATTCTCATCATATTCTACACTCCAGAGTGCCAAACCCTTTGACACAGCTGTAGGTCCAGCTGCCGCGCGGTCACATGCCGCAAGAATTACAGGGATTCTATCCGCGCTGATCTTGCCTTGCCCCACTTGCATCAGCGTGCCCATAATTATGCGTACCATATGCTGCAGGAAGCCACTGCCTGTAATATACGTATGGATAACTCCCTGATCGGAGGATCCGGGACGGCACATGCTGCGGTCCACCTCAAGACGTGCTTCAAATATCGTGCGTACATGCGAAGTCTTGGTAGACTTCCTGGACGCAAATGAAGTGTAGTCATGGGTACCCAGCAGTCCTGCCAACCCCTGCTCCATCGCCGGAATATCCAGCCTCATCGGATGATGATGCTGCCAGCGCCGCTGGAACGGGTCCGGGAACCGGTTGCCATTGATCGTGTACCGGTAGGTTTTACGCTTCGCTCCTCTACGGGAGTGGAAAGAGAGCGGAACCTCCCAGGCCTCGGTAACCACGATATCCTGCGGAAGCCTGGCGTTCAGAGCCAGACACCAGCGTTCCAGTGGGATCTGGGATGAGGTTATGAAATTAAAAGGTTGGCCATAAGCGTGCACACCCGCATCTGTCCGTCCTGAGCCCGTTATCTTGAGCGTCTCACCGGTCAGATGAAGAATGGCATGCTCCAGCTTGTCCTGAATCGTATTGCCCTGAGGCTGGGTCTGAAAGCCATCATAATGGGTACCGTCATAATTGACTTTCATCAATAGATTGCGCAT

Protein sequences of DBSCAN-SWA_8

>NZ_CP009285|7334467:7387354|7340794_7341208_-|WP_042217830.1|DBSCAN-SWA
MGYPEQIDVFQDRLNKKANGSSYVVEEKLLLAGGVYSGLLAHDNINNQTLSVYTGSRYSGTEVRNYSVSFPDEAPWRRMIKIYADVPEVYVTYETPGDTVEADDVNQLQSGLTATQSELERYKKAGLIDGGSFKREV
>NZ_CP009285|7334467:7387354|7376923_7379884_-|WP_042217881.1|tail|DBSCAN-SWA
MAGTGNSSGSINEIILQLNLLVTPAFQRSVGEAEHHIQDLDRVLQEMVSRGYFDVLRREADQADDSIEEVGDKAGKLGDKLKDAVKEVDFSMLQKAVEPLKAVWAAVNDSSGAMAQLQAATGLTAKEMSGMKDISNNLYSQNYGENYEDIGDAVGTVKQILQQTGEELEKTTQTAMTYRDVFKGDIAGSVQAVDAMMRKFGISSEQAYNLMAQGAQKGLNTSGGLLSAIGKYSDDFQKMGYSADEMFELLSAGMDNGADSLDGVADIVKKFGSNVKAGSDTAKAAVYELFAPKQLDQFSAALVSGGTKSKEFADLVKAAGQKGALALVGDLKAGGDSAKKAMLQLQKTLGGGDSLFKGLADGSITSKDAMNQVIVKLKAIKDPVHQAALAGTLFGSQFEEIGNKAVLALGQTRNQFDMTRQTMEEVAAIKDNTLSEQFAAMGRELMASLVVPMGENLMPALQGLTGWVSDNKEPLMVIGLAVPAAMLATKTVKIVQEFSKIITAARGASGAAGGIAGALGMLTNPLGLTVAGIGLAAAGVIAFRKHQEDARLELLNMGDALDESYSNYAGIEETTAKTQGLITEYDRLTGKLKDAKTPAAELAEARRKQKLVEQELIDMNPDILSAEDLKSGRFSDQLGLVGNLAKAQEDMSRRELEHDVLSAQAKLPDLEDEYTASTEKLAEQYAKYDTNMAKFQDYRQYVNQLDEIWNGKGSEKEKVVQIDALRDKINKAQGTEYDVSGGWAIESIKQDYEKYRTSFDDQYTEIKETESDKKEAESSMLSYYNAQKKLIELDLGGTLEEQVAKYKDLSIAQKEQITQALIDTASLNNEVDKLPAEKIVNVQVLWQQIGEVSNFNVAGDEGRKTANSKGKPYLPLYGGPKIAEYAEGGIAYVPSIFGEAGPEMAIPLNQKPRSRSLLEKANDLMGYNNNSGNNGDIHVTWAPSITLQGGDKSVVEQLREALKQTEDGFERRFKAMLQQQRRVSFQ
>NZ_CP009285|7334467:7387354|7373377_7374505_-|WP_042217872.1|plate|DBSCAN-SWA
MEYAELPEILFVEEDAAAIQQNVITIYEGLAGRTLQPADPVRLFLSSLAAVIVQQKVLINQTSKANLLRYASGTLLDHMGVFQGSKRLKASAAIVTLQFVLSIPLASVTSIPAGTRVGAQGGNGSIYFTTTEYLEIPAGETAGIATAQCSDSGTIGNGFLPGQINVQMDPLPFVQSVTNLTTSSGGAAAETDEAFKERIRNAPESYSTAGPQGAYEFWAKSTSSAILDVHAYSPAAGRVTVVPLLAEGQIPGEDVLSSIAETLEDRGIRPLTDLVTVSAPQPVSFNTAVTYYISRSRAAEVPGIQAAVSAAVAAYQLWQRSKLGRDINPSELIARIMAAGALRVVAAAPGYTVLSATQIAQTGTTTITYGGLADD
>NZ_CP009285|7334467:7387354|7386574_7387354_-|WP_042217891.1|tRNA|DBSCAN-SWA
MRNLLMKVNYDGTHYDGFQTQPQGNTIQDKLEHAILHLTGETLKITGSGRTDAGVHAYGQPFNFITSSQIPLERWCLALNARLPQDIVVTEAWEVPLSFHSRRGAKRKTYRYTINGNRFPDPFQRRWQHHHPMRLDIPAMEQGLAGLLGTHDYTSFASRKSTKTSHVRTIFEARLEVDRSMCRPGSSDQGVIHTYITGSGFLQHMVRIIMGTLMQVGQGKISADRIPVILAACDRAAAGPTAVSKGLALWSVEYDENEN
>NZ_CP009285|7334467:7387354|7370031_7372821_-|WP_052429718.1|DBSCAN-SWA
MAVFGGMTLTNKGLALQGKAQAGAQLNYTRIAIGDGSLSGQSVPALNALISLKKSLPIARLQMQPPNKVIIGTTLSNADITTGFYFREVGVFAQDPDGGEILYAYANAGVTADYIAPGGGTDIIEKAFDCVVVVGTAANIKAVIDESLVFAKKSELDAVDAAKVDKVSGKGLSANDYTTTEKNKLSGITAGAGGAASASDAVIGNRTISDATAPTGDSGTITTLLGWLANMIKSITGKSSWRTAPATTLEAAKAHADDATRHLTAAERTAWNAKETPAGAQDKADAAKTAAAADATTKAAAAQAAAATDATAKANAVQANLTSHIGSGGAAHAVATTTVAGFQSAADKAKLDGVAAGANNYTHPATHPPGIIVQDASNRFVTDTEKSTWNAKASTAVATTTTAGLESAADKAKLDGIAAGATVVANSASNGVITINGTNATVYTHPNHTGDVTSTGDGVTAIAAGVIVDADVNAAAAIAWSKLSKTGASLADLPTRSAADLSSGTLAAARLPAISGDITMAAGAGTATITAGAIVNADVNTAAAIDATKIGTGVVSNAEFGYLDGVTAGIQGQLNTKANLTATPQQTTADITYYVRTDGNDGNTGLANTAGGAFKTIGKAISMIPQVVNHTVAVNVAAGTYAEDVIISGTNGAGYVAFNGTSASIRSFTAARCIRVVVNGFTATSTTQSPFYAYDGGKCDFTSCIVNASSANTGITFFNQCGLVEGCTISNRSVAIHVEKGQVTVINCAGTGNTTAILPSGGALVNTSGTIMSGALDGANGGVINPWGDNTWSARSFIYGTHNAQQTIATNVWTKVIYGSEGNDNLGEYDPTTGVFTAKMAGVYAITASIQFTNATGGAELKLAVGSSSGVTSVISHTRPGSSGYTAASGALMLGVAAGGTLAIWMTSTAGATTNPDGAYSYVMITRIA
>NZ_CP009285|7334467:7387354|7344709_7346542_-|WP_042217841.1|DBSCAN-SWA
MEITSTALVPVTALTVWQNVNSQWDRLNQNFNRASHSLGDLQQILERIYEEKNKSFMEGFMQSQEAARRLADEGDSSRSQRSAGSSNDDDPDNNDVRNAKSGFMGEVQKIMKALDVGGFELITYVGEKAIGYMQNKKKEAAAEKEQKAAEKARKAAEPGFLSKTKDSLGSLDLGGVFDKVKSLGTKAIAANATEEDKGKWNKLQGNMDSAVEMMGQKAIVALRPILDTLNNAFQSEGMSTALNLIANAFLVIATVIGEVVNGILYMFTAFQENWDVVGPILAAIAIVFIAAMIVQLYNLAAAWLVGMWPILLIVAAVALLIYILQQAGVSVNEVVAFIGGAFGWLRATIENFVIGLYNNFVSFADFFRNLFIDPTYAVQKLFYDLATNFLGFIYQMALGVESFAGGFVKAIAEGINFVLKGIQVMAGWLSKFPGFEFLADFKPNFLEAENPHVFSDMVKNAQGTLVEPTSTKDVYNTKKKEFVDTAKTVKEYGDKASALPAKFNTKLDRVKPKDDKSQNPAQAAAANINSVNKVGEVGSINEKVDISSDDLDMLRELAEIQSIQNFVELTPTVQVTTGNINNSGDIDSIITKIGQKLKEEFVSTAQGVYT
>NZ_CP009285|7334467:7387354|7374834_7375233_-|WP_042220130.1|tail|DBSCAN-SWA
MNKIGSLGPVVFVVAEGAIRTIDEFKRSSSSRWAQHDIIGQKPKKEFVGPGADSVSFAVHFSAALGLNPRKELDRLTELDRAGKAMPLVIGRKNVGVGLWVISGLSQDWSRLDSIGNVLDAQVTISLEEYVK
>NZ_CP009285|7334467:7387354|7361957_7362548_-|WP_042220127.1|DBSCAN-SWA
MNLRKWFYLFWTTLLIGAGGAVIAGLALQTVNGGIDFKSTADLLLYALILFGYGVLVSVYAQLGFFAYLILNYMGIGVFPRKAWRYIQLVLAVLALLELVFLRTFVSGDRSVASDLILGVGILLTAIVVSGFKMRGTNASAWIPTFFFMTAITIVEIIGVLRIGVDSATIFILVPLVACNAFQILMLHRVLKPASI
>NZ_CP009285|7334467:7387354|7334467_7334731_-|WP_042217817.1|holin|DBSCAN-SWA
MINSELFDNVLAFASILAVVILALVQLIKNNTRLSRNVIPFVGLGIGLLVGAAAYPFTDLDITLRLWAGGLAGLSATGLFELAFNNR
>NZ_CP009285|7334467:7387354|7368936_7369242_-|WP_042217866.1|DBSCAN-SWA
MDNNNVLNLEKLLPLADKYGLAYILALVLVFVVFGFVRDIRRGKWVPRELLDRAEEDRDRLQSILDKERSDFMAPTLQVLQGLKIDHAASNNAGNDEDRGG
>NZ_CP009285|7334467:7387354|7349058_7349265_-|WP_052429717.1|DBSCAN-SWA
MSSNEMKASELKRSGEGRNAFGKKQIMGSVVFTPKEKDVLEVVLQESGSYTLEEAKQLIELYLTKEVI
>NZ_CP009285|7334467:7387354|7375689_7376721_-|WP_042217877.1|DBSCAN-SWA
MESMQDARRAVLELRYNGKDVTVDIAKSLTDFQYNDAASGSLDDLTVSLEDRDRNWQGPWAPVEGDQLVASIRTVNWGKPGEIKKLPLGTFEVDSIDFNGPPDTISIKAVSLPITSEIRMQRSSRSWEKTNLKTVAAQVAKRAKLKLIYEAQDNPSYERLEQSEMSDLAFLLNTATQEGIAIKVSGGSVVLFDEREYEQKAAVATIVRGEANVTGYSFALNTAYAAFRACTVTYTPPQGKEPLKATYTPEGAPKSGPVLKINEQVDSQADALRLARKRLRERNKEGGRGTLSLMGDMRMATGLTINIKGWQRFDGKYIIESARHSIGSNGYTTNLEIRKVLGW
>NZ_CP009285|7334467:7387354|7346734_7347157_-|WP_042217843.1|portal|DBSCAN-SWA
MSELSLFFAQNAACDTTEEFVVSLRFKDKEGKAAVWKLRSMNEDENQECRKAATRKVKGKNGTYSTEIDPNEYMAKLMTASVVHPDLKNTELQRSYGVMGAESLLRKMLLPGEFAALGERVQALNGFATDMNELVDDVKN
>NZ_CP009285|7334467:7387354|7336481_7336919_-|WP_042217823.1|DBSCAN-SWA
MSYFCAYDIRDGVGYVYATYHDTESLEGVDGVTVDVLPEPIDNGKDPVLKVNLTDARLYYDYEEPKTADPYTPKVIELEQRITNTELDLAMTQLALTETFEELQVTRQEAADSQLALTELYELMLAGQTGLEAEQTTKGGDEDNG
>NZ_CP009285|7334467:7387354|7350884_7351328_+|WP_042217848.1|DBSCAN-SWA
MAEEFGNYLKQLREDKGLTINQLASLAGISGAQISRIENGLRGVPKPATLRKIADATDVSYEELMGHAGHLTESESSTEGAVPAWATSKDKRDFRQMLEDDGELMFDGIPLNKEDKQRIKDVLTGLFWEAKQMNKRTKPKHDSGTKE
>NZ_CP009285|7334467:7387354|7374508_7374838_-|WP_042217874.1|DBSCAN-SWA
MMYTVDMTQPTLINFSPLTVEEEVSQNIRMILATPWGSAPLVREVGLDYTIIDEPAFIAETRLTAEIITAITEQEPRASVADVSFHKDKENSLNGRLAVVVKYTLAEEE
>NZ_CP009285|7334467:7387354|7336931_7338797_-|WP_042217825.1|DBSCAN-SWA
MKTTGNLGLKKPDGTDIVDITDLNGNMDILDTAVKAVQDHAADAVKHITAAERTGWNAKASTAAATASAAGLMAAADKAKLDGVAAGANNYVHPNHTGDVTSTGDGVTAIAPGVIVNADVNATAAIDATKIGTGIVSNAEFGYLDGVTSGIQGQLNGKSPTVDYVRQPAYSVTAGTGAAYTVNLTPAPASLPEGFGITIVPNLVNTAGATLNVNGLGAIPLKDQKGIAYAAGKLLAGKPYMFRKVGTDFLADSAGGSGNAVAGDIRAGKTAATDAGDVTGTLAVQTGGTVTPGASAVVKPAGIYDTAITVAGVSVPAASVLTGTTIAGTAGMMPNRANDQVAARVNYERVGRVAVGFPTGGYLTNSGFGAGIASVAVEDSGLNPAYVRSDVSILGMQGSMPVISTGADVALSVGKWGDGALAVYPREGYRKGGAGAGEIKVSVDQLKSVNAHLQPWYIAQGAEIFGVYGTVAPALSGRIDISFSSGWVAGDGRAYLICSMPAGTKRFTWSGSSTVYYDYGRFSLFVQDGWTGAEVGWINMERGGNLYLYPTGMMYDAAKRTLTIWSASTYNGGNMISTAPSTYNLPANFNTDAPLNLYFRADWAYSYSPTMSLSGSITYSN
>NZ_CP009285|7334467:7387354|7342261_7342690_-|WP_042217833.1|DBSCAN-SWA
MIPAIGRSGPVTAALEGSTAASGTSPSLTYRMDFEHKRIAGRIDGLEAVKQAAVKVLQTARFEHLIYSPNYGTEWSLVLGQDRLLARPELRRIVSEALLQDERIQQLEDVDILFNGDTVSFSCTAVTYYGNFELRKEEIAGV
>NZ_CP009285|7334467:7387354|7347264_7347735_-|WP_039294168.1|tail|DBSCAN-SWA
MTFLKASDTLSGQEGRAYATINGQTEEMFYVKTLEATVEKQKAEVKTLGRRGVQHKATGWSGSGTMTIFYMTSRFRQMMLEYMKTGIDQYFSIIVTNEDPSSTVGAQRIMLKDVNLDSVIMASLDTESDALEEEVSFTFEDVELVQPFSAPANSGQ
>NZ_CP009285|7334467:7387354|7358936_7359167_-|WP_025336637.1|DBSCAN-SWA
MLGMLFNEKECKELDYVLRKELDEMLLDLSDQRLDQNIRHAIANRYKTVFRMYARFAPQKELSKYAWGGRSSQFKH
>NZ_CP009285|7334467:7387354|7380033_7380354_-|WP_042217882.1|tail|DBSCAN-SWA
MGTKNIEEAGAEVYTFARPVTFEGDTFESLSIDFDKLTGEDILICDRQYQVESARQSSGELIKETNKAYQAYIVAKAAGVHVGLIRALSAKDFTKLTLRAQSFLLL
>NZ_CP009285|7334467:7387354|7362675_7363368_+|WP_042217853.1|DBSCAN-SWA
MKWRTLWSGGLALGLVMALTACGGEQSSSSSGQGGYKEMKTMVVDILKSDEGKKAVEEALSTPSSGESSTSGLSMKMMPMQTTEQIRIAVKDTITAPEYQKEIEKIMTDPQFAGEFAKAINTQSKELHLQLIKDPTYQKSVEEIMKSPEMMKMFLDLTKTSDYRKQSMTIMQEAMQNPLFRMEVLDLLKSVVQEELQPKVQKKDAEKSGGEGQGSGGDSQKQEGGDDSGS
>NZ_CP009285|7334467:7387354|7350110_7350593_-|WP_042220124.1|DBSCAN-SWA
MILASLPELDRRLTQVTIENMLEKYRIFKTVTFEAKEAGITYSYMERFHGATNSVTDQTAAIATHNVDVPAARRAYCAMIDSVVERLTLREQQLVRERYMRREESYDYTIYNHVFDPPVSKDTYVKIRSKAFYKMALALADLQLLSLATLEKTTGASREK
>NZ_CP009285|7334467:7387354|7338808_7339420_-|WP_042217827.1|DBSCAN-SWA
MAYGDSIYGLLEYSTDGVTGEGPEVIVPDLMKYLPEYYQGVPEMEQLQASAGAQCGELAYAMADSDAQKTLESATWSLSRWERMLALTSDTDKSYATRREMIKAKLRGSGTTTPEMIRRTASAFSGGDVEVVEVPGAYSFEVRFVGTLGIPANMAGLIQILEEIKPAHLDYSFVYSYTWWDSVKTLTWNSAHARTWNELRVYE
>NZ_CP009285|7334467:7387354|7351370_7351784_+|WP_042220125.1|DBSCAN-SWA
MDELIKRLVKKYKTNSPFELAGALGIHIRFMNLGEGTKGLYYRKLKRRFIVIHNELPLEWQRFVCAHELAHDRLHKGVNRFFLEENSYFSSGKLERQANLFAVKLLSAGTSIEQEESLQSYYARIGIPAEVVFFLDD
>NZ_CP009285|7334467:7387354|7368372_7368750_-|WP_042217863.1|DBSCAN-SWA
MGGIDILLLIAYFISFICALLLMAALFLYFRKRFRARVVSLFMLAAFFFLGAYTVKMAVAFWIRFSITSGDSAVYAALKSQGWAIAQTGTTLGLVILTVLMYTRRQDLFMIFPAVKEEAKRDADA
>NZ_CP009285|7334467:7387354|7369496_7370009_-|WP_042217868.1|DBSCAN-SWA
MNIALAIMYLYPNADPMRDFRVQNNGPEPVLRPGAEEKGRVRYEIKPPEEGEEPIEGIHYRYGIDYNLLTEGEDYDLVERGPYIALWNLDEPQPTKAELQAAWEAYQEAEANKPPELTEIEQVREELAQTRIALTKTYEQLQSAQDEATGAQLALVELYELVLPLIGGDV
>NZ_CP009285|7334467:7387354|7367599_7368124_-|WP_042217861.1|DBSCAN-SWA
MKTGKLMLVILLLITIIGCSSDQQNFTKTNDTIKEYIDTAKVPAIPGLEVESIFVNLDKETKEGLRNTVVITYTDEKGKLIKNVNTESNVSVIYGPYEGKKVLTLSISKAEVEYGNEMQTKSIYNLELFYTKVQDNLLIYTRHDGLSFTSEGRITNEYTEEQHFEMFTQAVTNN
>NZ_CP009285|7334467:7387354|7335984_7336326_-|WP_157764177.1|DBSCAN-SWA
MTNIEGSEAMDSNDVANLEKLLPLADKYGLAYIVALILLMIFLVLLRSIVKGNLVPRELLERAEEDRDRLQNILDKERSDFMAPTLEVLQRLKIDHSAGDKNSGSINEEDRRG
>NZ_CP009285|7334467:7387354|7385903_7386341_-|WP_042140128.1|DBSCAN-SWA
MRTTYMAKPNEVERNWHIIDAEGKTLGRLASEAAALIRGKHKPQFTPHVDTGDFVIVINAEKIHLTGKKMQNKKYYRHSMHPGGLKVTVAEDLIKTKPERMIEFAVHGMIPKTRQGDHMKLRLKVYAGAEHPHAAQKPEVYELRG
>NZ_CP009285|7334467:7387354|7360152_7360956_+|WP_042140121.1|DBSCAN-SWA
MNSFYVFSGKKIKRFIYIFAAALLTAGVVYVERGNITVFSEAAPSAIYSVPTEKKLIALTFDISWGEKRPEPILKVLEDKKVDKATFFLSSPWSKTHPEIVTSIKDAGYEIGSHGHKHVNYSTLSNEEIRTQITTAHTVLTELTGTQPNLIRMPNGDFDKRVLQVASDLGYKVIQWDTDSLDWKNIGVDNIVNRVTSKAHPGDIVLLHASDSCKQTHEALPQIIDKLRSQGYEFVTVSELISQSSADGKEVRDSAWLDNGLEDAAGM
>NZ_CP009285|7334467:7387354|7335785_7335983_-|WP_039294209.1|DBSCAN-SWA
MLSEWIKRLSPLHRDRERKLTQAGMRVSLSIRRYKNVSKEIQEEIRNNGFAEFLIYDRGAEDEHH
>NZ_CP009285|7334467:7387354|7376726_7376927_-|WP_042217879.1|tail|DBSCAN-SWA
MIYRTVQGDMWDGIAFKLYGDAQFMALLLNANPAHAPVSVFSSNIVLNVPELPADTSSSLPPWRRG
>NZ_CP009285|7334467:7387354|7366676_7367369_-|WP_042217860.1|DBSCAN-SWA
MNLLEKEDLIKVKAEELENATPQEIIRWAVETFPNITFACSFGAEDVVLVDMIQKVSPSTDVFYLDTDYHFKETYETRDVMAGKYGMEFVRVSPQITVEEQALQYGEALWNTDPNQCCAIRKVEPLTRILSQYDAWITGIRRDQAPTRANAKKVEYDNKFGLVKFNPIANWTTEDVWNYIRENDVVYNPLHDRNFPSIGCEQCTRAVMPGEDPRAGRWAGSDKTECGLHK
>NZ_CP009285|7334467:7387354|7365465_7366641_-|WP_042217858.1|DBSCAN-SWA
MTSILPHGGTLIQRYAAGEQREELLQQASANKSIALNTWTLSDLDLIGVGAFSPLTGFLNEADYQSVVTSMRLADGTVWSIPITLAVDDKQAASLAVGDRVSLIGEDDGIVYGLLDIESIYEVDQQLEAQNVFKTTDPEHPGVSKLLGRPATYVGGPITVLNRPQPEKFAEFYFDPAETRQIFADKGWRTVVGFQTRNPVHRAHEYIQKCAMEVVDALFLNPLVGETKSDDVPANVRMKSYLALLENYYPENRTFLGVFPAAMRYAGPREAIFHAMVRKNYGCTHFIVGRDHAGVGDYYGTYEAQEIFANFTAEELGITPLFFEHSFFCVKCGNMASSKTCPHPGDQHLTLSGTKVRALLRDGQCPPPEFTRPEVAQILIEGMSPEVSVKS
>NZ_CP009285|7334467:7387354|7339422_7339758_-|WP_081970300.1|DBSCAN-SWA
MALKTLIQIRRGLESALGTLAAGELGYCTDTGKLYIGNGSSNLLLVAAQSTGDMLKSIYDTNNNGKVDYAQAADSVPWSGVDGKPSVFPPAAHTHEYMPKGPLTWNQLKGV
>NZ_CP009285|7334467:7387354|7339770_7340793_-|WP_042217828.1|DBSCAN-SWA
MAQTIQVKRGTRAELSTYGTLKAGEMGFCTDTKEIYIGDGTSNSMVGRALSGPEASRPAAASVGRLYYVSSGSNSGYLYFDDGAAWRRVNAQKLTDLTGTVDDIADGTTYAKVLKADITAGHPNKVSDGTNTKTAAEIKTHIDDATKHRLINDTGTAITDLWSAQKIKNEIELAKHNIEPQASVKDQNLTAPPASPVEGERYIIPAGATGVWAGKTNQVAEYQSAVWVYYVPVVGWTAYVDDEQKIYSWNGTAWVRTGGALQTITAGNGLTGGGQADAVTLNVGAGNGITVSADAIAVTAGKGITVDAAGVAANVDGSSIVYDAGNGNRLTVGSIDGGTF
>NZ_CP009285|7334467:7387354|7343961_7344708_-|WP_042217839.1|DBSCAN-SWA
MEEYGFYLSFNNYEEVIRLPVNPETLEIKENGDSKSYTVVDFGEINAIAYPKLTEITIESIFPAQYYPFVVYSGENAGKLLKPYEYVELIRKWMLSRRPVRFVFSGLKAVNVQDTQTPDWLKQASTQAQQTFTGDIGINMAVSIESFSWKLSAGSSGDIEYTIGLKKYVFYQALAMKVDSKGEVKTQQKRASEKTAPSTYTIKAGDTLWSIAQKHLGDGSKSKTLQKLNSIPDSELKKLKPGRVIKLS
>NZ_CP009285|7334467:7387354|7341210_7342269_-|WP_042217832.1|plate|DBSCAN-SWA
MYEDQTYEALLERMLDRVPEGMDKREGSIIYDALAPAAAEMAQMYIELEVSNNLYFPDTAGGEYLERSIAWTGITRHPAGKAQLSGKFYTSGGELLDIPLGSRFSLGLLHYSAAEKLSPGMYRLESETAGSEGNQYSGTLLPIDYIPGLARGEITALLVPGTDAESDGALRQRYFDSARRPSTSGNKYHYMEWAQDIQGVGGARVFPLWAGPKTVKVVIVNAEHKPASALLVSQVQQYIDPAPGLGEGQAPVGAVVTVESATGKTINVTAKVTLAAGYALQPVINAFTAILEKYRKEKAFAATYISQSVVGSLLLDTDGVVDYSGLKLNGGTGNVTLTETEVPLFGSVVLEV
>NZ_CP009285|7334467:7387354|7382347_7382632_-|WP_042217888.1|DBSCAN-SWA
MNFINNKDNLQNEQEPAQEPPQIYLGPNLRGGRLLQSTVFREGIPSYLLPLLEEQPDVAELIIPLEEITAVQERIVQAGTAEYAVYQRLLGKGI
>NZ_CP009285|7334467:7387354|7342986_7343949_-|WP_042217837.1|DBSCAN-SWA
MELIVINKEGTIWDVSGIATDISWKTTRTGKPATLELTLADSGIYQHAKFGISNGDIVQFRKDGIDVFYGFVFSIDTGANQEIKLTAYDQIRYLLGNGSYVLQNITASELIRKVAADYGLRLGVLDPAKYTIPSLIEDNKKLLDIIMGAVGSELQYMGQLMAFYDDFGKLTLRAPQAMLLNVILGAGHYLYDYSLKRSIDDDTYNTILLYQDNEETGKREFFPATDKENVERWGILHLYQKADDKANAAQIQEKAGNLLKLHNREKLSLSVQAIGDMRVRAGNFIYVLLDEFETQLFLVDQCSHKISGGEHTMSLDIKVV
>NZ_CP009285|7334467:7387354|7359409_7360021_-|WP_042217851.1|DBSCAN-SWA
MLSFNTFIRDLGTIRKALLTAALLFIAGGVIGWIGTGSLQQLLNEQLKGISEISGDLRESSNPQWSFFVFIFLNNSIKSVVIIFLGALFGILPVLFLLINGAVIGYLIHLSAIQGQDLFTLIVKGLLPHGIIEIPAIIIACAFGLRFGGKALSALLRAGKRNEREADHWQAFMRQTFTASVWIVILLFIAAIIESTITFSLLS
>NZ_CP009285|7334467:7387354|7334727_7335438_-|WP_042217818.1|DBSCAN-SWA
MLTLIQVLNKSAARLSGLHPAVLAAATTLIERCYACGVPILITQGLRTIAEQDALYAQGRTKPGAIVTNARGGYSYHNYGLAVDFALLLPNGSSVSWDMNRDGDSDCTADWLEVVQQAKAIGFEWGGDWTSFKDYPHFQLSFGLTLAALRTGKKPAAAAVEAVYERIKLKEEQTVKSEITAAVKVNGVKIAEGMMVNGITYAPVRVIAEALGAQVGYNSATKTVDIISSGLKGAGS
>NZ_CP009285|7334467:7387354|7383226_7383700_-|WP_042220131.1|DBSCAN-SWA
MQKLIPEYQISLKGVEQLYRSAEAEDKKVIAGMVSDCEYVIEWLSSGRRPGNKRGIERRAGYEREILLEPILMQNFTCHFNAVPSEGLTEDQRFQLEYVLGLLSRREKECYMLANGEGFSHVAIADMLQISAGSVSEYIQRAQKKISSVIDEYRSLI
>NZ_CP009285|7334467:7387354|7363447_7364557_-|WP_042217854.1|DBSCAN-SWA
MLTREQIQELLQPLTDPESGKSLVELQLIRDIMIKEDRISLSIVCLDTDEKKRMELEQQVRDLLAAAHAGNVHIRLRDATDYERAILRGESAEDEQEPEQGEKLKGHAAGLEGHELINENSGVNFIAIASGKGGVGKSTVTVNLAVALARKGKKVGLIDADIYGFSIPDMMGIEEGPIVEEGVIIPVERFGVKVMSMGFFIRENSPVIWRGPMLGKMLRQFFSDVGWGELDYLLLDLPPGTGDVALDVHQMLPHSKEIIVTTPHATAAFVAARAGSMALQTEHEILGVIENMAYYECSSCGKKDYIFGRGGGARLAETLHTELLAQVPLGAPDNHISEPDFSPSVYKADTPTGGLFAEIADKLIAKYEQ
>NZ_CP009285|7334467:7387354|7380898_7382344_-|WP_042217886.1|tail|DBSCAN-SWA
MAFKHGVTIIEQSTSVLAPTKATSGIPFAVGTAPVHLAAASVPVNTPVLVYSYAEAVAAFGYSEDWSKYTLSELIYSHFALYEKAPMILVNVLDPATHKTTVAPTAAAVTNRDAILQAEGVLLSTLLVKSSDGTSTYVSGKDYTAAFDENGHVMISTKPSGAIAANVNQLSVGYDKLNPEAVEAEDIIGGVTPSGEYTGFELVHQAYPRFGILPDLLLAPGWSHLSAVAAVMKAKAGNINGNFKAMALTDIDPSQSYTDAGTWKADNSYTAPLQVAAYPMLTLGDKKYHFSTQLAGLIAATDANNGGVPFVSPSNKSLQADGTVLSDGTSQFLGIDQASFLNSAGIVTALNLGTSGWKSWGNHTAAYPGATDPKDSFIPVRRMFNWIGNSLILTYMQKVDDPMNKRLVAAVTDSVNIWLNGLTASGALLGGRVDFNESENPVADLMAGKVTFHLHITPPGPAQEISFLLEYDTTYLAALVA
>NZ_CP009285|7334467:7387354|7375258_7375696_-|WP_052429719.1|plate|DBSCAN-SWA
MVELILIGRVSTVNVAAGSVRVSFADRDDMVSGELPVLTPGGWGRGNAIPLPGERVLCVFLDNGRSAGFCLGTYFAEDDQPSGSKDQRGVWFEDGSYVYYDRTAKRLNVKGSGGVRIEGDLTVTGKVSASVFNDGGVVEQDEQYS
>NZ_CP009285|7334467:7387354|7383950_7384349_+|WP_052429720.1|DBSCAN-SWA
MQRAEVLKRLIEETGLNTKAFSEKAGIPYTTLRSILMRGVGGASVDNVLKVCRALGITTEEMDRLAFGSSKEEAAPLLSELSEFEAFLNNPEHGLFFKDYLDAPDERKREMLTFWQFIKDLEKKKSDSSDDN
>NZ_CP009285|7334467:7387354|7342686_7342980_-|WP_042217834.1|DBSCAN-SWA
MLDIIKQASLGAVSNTNPVAFSYGTVVGAQPLQIQVEQRFILTGPALVVPESMMESRTLFEGREILLRRGLAAGDRVLLVRMQGGQSYIVLDRLVDL
>NZ_CP009285|7334467:7387354|7335409_7335799_-|WP_042217820.1|DBSCAN-SWA
MSIIDIVLLIAYSISFICALLLIAALFLYFRKRLRARVVSLFMLAAFFFLGAYTVKMAVAFWIRFSTSGSDAVLSSLQSEAWAIAQTGTTLGLVILTLLMYTKRQDLFVVLSGIRKGRNPHADSNSGSK
>NZ_CP009285|7334467:7387354|7364646_7365393_-|WP_042217856.1|DBSCAN-SWA
MSGRQQHKVSVWISWNSIKKSILGAVLLAVMIGIIAYDMPTAKTINYWSLPLSGKVIAIDAGHGGPDGGAVSREGLIEKDINLSVSLYLRDYLQQAGAIVVMTREGDYDLAQDSTKGYAKRKTEDLKQRVRSIEEKGADLFISVHMNSIPSNRWSGAQTFYYPSNEGNKALAGLVQDELRATLENTDRVAKTVNTVYLLKALKMPAALVEVGFLSHPEESALLGDDVYQRKVATSIYRGILRYTSEQP
>NZ_CP009285|7334467:7387354|7380366_7380885_-|WP_042217884.1|tail|DBSCAN-SWA
MPKRSERVIDYSVYLNAVDYLGTATATLPEITYLVDTIKGGGIAGEMAAPSPGHTGAMSLALKWRTIEKAAASLLAPKIHTLDLRASIQTFDTATSEYREVPFKVTVRARPLGLTLGNLETAAVMDTTNNFSVNYLKVTLDGVQVLEIDKYNYIHKVYDVDYLAATKENLSL
>NZ_CP009285|7334467:7387354|7347736_7349059_-|WP_042217845.1|tail|DBSCAN-SWA
MAGGTWTTQNKVRPGVYVNVASNGSVAGKMGERGTAALALTLPWGQAGVILKLTAQEDFKQKLGFDLTDAQLLPVREVLKRAGTLLLYRLNQGVKAAVTNNGVQATALYGGERGNALKIVIEKNIDDNAQFDVRTLLENTEVDKQTVATAAGLAANDYVEFKPNGPGALTVTAGMPLVSGANGTVTNTEHSDFLSALEVQDFQTVGLVSEDNTLKALYSAYVKRLRNTEGKKVQAVLSDYATADHEGIISVANGVVLSDGTVVDKAHAVTWVAGATAAAAVNESLTYQAYDDAVDADVRFSHSETVAALTDGELLFTYNGGRAVVEQDINTFTSFSPDKGKAFSKNRVLRVLDGIAGDLKRIFENYFIGKLPNNEDGRALFWSQCVTYMNDLQNLGAIENFNAQSDIVVTPGADSDSVVLDVAVKPVDSVEKVYMKVKVV
>NZ_CP009285|7334467:7387354|7349261_7349684_-|WP_042217846.1|DBSCAN-SWA
MAVQQLRENITDALAQFYPDIPVYVEGDKPQSAYFKPGLISATYDRQREGRYMAVYRFGIRYEQGSLLEAESMADGLCEALAVRESGNSSFRVIRQSWEAGTEGHGPLFTVDYMLYLQKQKQPQDEAELMGHFTEGAWLK
>NZ_CP009285|7334467:7387354|7382628_7383051_-|WP_042217889.1|DBSCAN-SWA
MTITLLIMAIQKYLKEQLADDMLPVPSVLLGYLPQSDAGNPGYPVIKIRPAEGEGDSGQGQIQIKLQFGAQSEDDTGLIDMLNLMERVRILLLRKRVLEQKFVMDASWKMKLNEEHPAADWGGELTTTWVLPQIRPEVQI
>NZ_CP009285|7334467:7387354|7384435_7385332_+|WP_052429721.1|DBSCAN-SWA
MFIHYKKTHLEHFVEKLYINHSILKPEDITIQRLSTELDIHIDYAPVRSRAYESITGMRFVLLDNRITPMKQRFDFLHELCHMLRHAGNQMTLPVPFIKAQEEDAEKFVLYATMPFFMIQSFSLSGDYSTAIQQISNVFGVSREMAKVRFDQILRREYEGEMLPWRRGEYISHSFDQKNSEPSHALDEPVIFAYYDPHSTLDGPDQLIVCLDHATLSTQHEWIVPMEERFKEIEIDALKNLELESASRGDLICFDGQLTLQIHQLVYRHGLSKRNFVLQMRDIEQILEADQSTVRRFL
>NZ_CP009285|7334467:7387354|7385490_7385883_-|WP_042140127.1|DBSCAN-SWA
MAQVQYYGTGRRKHSVARVRLVPGEGRIVINKREMDEYFGVETLKMIVRQPLNLTETLGNYDVIVLAHGGGISGQAGAIRHGISRALLKVDPEYRGALKKAGFLTRDPRMKERKKYGLKAARRAPQFSKR
>NZ_CP009285|7334467:7387354|7372833_7373385_-|WP_042217870.1|tail|DBSCAN-SWA
MINIQTVSLFDLLPLPIRNDPAMAAAAVALDIQLQETSRMIAGLELFGRSAEWTNAEADELAWQFKPPYYDPDLPLDQKRLLIQNAIPFHRHKGTAGAVEDLIAILFGQGAVEEWWQYGGDPHHFRVVTNNADVTAERAQEFIAAVDAVKRLSAVLDSVTISQAEQLPFYFGGFLHFGEHITI
>NZ_CP009285|7334467:7387354|7361004_7361826_-|WP_042217852.1|DBSCAN-SWA
MNIKRYMIKDTSETRLKDLDPNERGEFKSKEEAEAKMEKLKKRLAELQDILFAQKKHSLLVILQGMDSSGKDGTVKHIFSGINPQGFIVTSFKKPSLEEEAHDFLWRVHMKTPPKGYIAAFNRSHYEDVLVPRVHGSLKKEDAKRRFRYIRQFEEMLAEEGTTVIKLFLHISKEKQLEKIQERLHDPAKHWKFDASDLQEREYWDDYQKAYEDVFEQSSIEKAPWYWIPANHRWYRNYLALAIVVKTLEGLDLSYPKLNTPTPDISELISPRH

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042217817.1|7334467_7334731_-|holin	holin	A0A0U4JE55	Bacillus_phage	2.6e-14	49.3
WP_042217818.1|7334727_7335438_-	M15 family metallopeptidase	A0A127AWA8	Bacillus_phage	4.2e-43	56.0
WP_042217820.1|7335409_7335799_-	hypothetical protein	NA	NA	NA	NA
WP_039294209.1|7335785_7335983_-	hypothetical protein	NA	NA	NA	NA
WP_157764177.1|7335984_7336326_-	hypothetical protein	NA	NA	NA	NA
WP_042217823.1|7336481_7336919_-	hypothetical protein	NA	NA	NA	NA
WP_042217825.1|7336931_7338797_-	hypothetical protein	S6B1J7	Thermus_phage	1.9e-26	31.8
WP_042217827.1|7338808_7339420_-	YmfQ family protein	S6BFJ0	Thermus_phage	2.8e-43	52.0
WP_081970300.1|7339422_7339758_-	hypothetical protein	A0A0A7S181	Clostridium_phage	2.5e-06	68.6
WP_042217828.1|7339770_7340793_-	DUF2793 domain-containing protein	A0A0K1LM54	Rhodobacter_phage	1.2e-11	36.8
WP_042217830.1|7340794_7341208_-	hypothetical protein	A0A0A7RW10	Clostridium_phage	3.4e-29	48.4
WP_042217832.1|7341210_7342269_-|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	5.6e-92	52.6
WP_042217833.1|7342261_7342690_-	DUF2634 domain-containing protein	A0A0A7RTU4	Clostridium_phage	3.0e-20	42.0
WP_042217834.1|7342686_7342980_-	DUF2577 domain-containing protein	S5MC71	Brevibacillus_phage	7.1e-13	39.7
WP_042217837.1|7342986_7343949_-	hypothetical protein	S5MNC9	Brevibacillus_phage	9.2e-86	46.9
WP_042217839.1|7343961_7344708_-	LysM peptidoglycan-binding domain-containing protein	A0A0K2CNM3	Brevibacillus_phage	8.9e-44	43.7
WP_042217841.1|7344709_7346542_-	hypothetical protein	S5MNW9	Brevibacillus_phage	2.9e-40	33.3
WP_042217843.1|7346734_7347157_-|portal	phage portal protein	A0A0A7RTY8	Clostridium_phage	2.3e-12	38.9
WP_039294168.1|7347264_7347735_-|tail	phage tail tube protein	A0A0A7RVP1	Clostridium_phage	7.5e-49	60.9
WP_042217845.1|7347736_7349059_-|tail	phage tail sheath family protein	A0A0K2CNL4	Brevibacillus_phage	1.1e-110	47.7
WP_052429717.1|7349058_7349265_-	hypothetical protein	NA	NA	NA	NA
WP_042217846.1|7349261_7349684_-	hypothetical protein	NA	NA	NA	NA
WP_042220124.1|7350110_7350593_-	transcriptional regulator	A0A0C5AN03	Paenibacillus_phage	9.4e-39	61.2
WP_042217848.1|7350884_7351328_+	transcriptional regulator	S6C481	Thermus_phage	1.5e-19	41.9
WP_042220125.1|7351370_7351784_+	ImmA/IrrE family metallo-endopeptidase	Q9T201	Bacillus_phage	3.9e-17	37.5
WP_025336637.1|7358936_7359167_-	hypothetical protein	NA	NA	NA	NA
WP_042217851.1|7359409_7360021_-	stage II sporulation protein M	NA	NA	NA	NA
WP_042140121.1|7360152_7360956_+	polysaccharide deacetylase family sporulation protein PdaB	NA	NA	NA	NA
WP_042217852.1|7361004_7361826_-	polyphosphate kinase	NA	NA	NA	NA
WP_042220127.1|7361957_7362548_-	KinB-signaling pathway activation protein	NA	NA	NA	NA
WP_042217853.1|7362675_7363368_+	hypothetical protein	NA	NA	NA	NA
WP_042217854.1|7363447_7364557_-	P-loop NTPase	NA	NA	NA	NA
WP_042217856.1|7364646_7365393_-	N-acetylmuramoyl-L-alanine amidase CwlD	A0A0N9SGH1	Paenibacillus_phage	3.9e-15	34.8
WP_042217858.1|7365465_7366641_-	sulfate adenylyltransferase	A0A2K9L4R9	Tupanvirus	3.9e-46	34.3
WP_042217860.1|7366676_7367369_-	phosphoadenylyl-sulfate reductase	NA	NA	NA	NA
WP_042217861.1|7367599_7368124_-	hypothetical protein	NA	NA	NA	NA
WP_042217863.1|7368372_7368750_-	hypothetical protein	NA	NA	NA	NA
WP_042217866.1|7368936_7369242_-	hypothetical protein	NA	NA	NA	NA
WP_042217868.1|7369496_7370009_-	hypothetical protein	NA	NA	NA	NA
WP_052429718.1|7370031_7372821_-	hypothetical protein	A0A0C5AEQ0	Bacteriophage	1.1e-46	58.0
WP_042217870.1|7372833_7373385_-|tail	phage tail protein I	A0A0C5AJ63	Bacteriophage	8.0e-50	53.6
WP_042217872.1|7373377_7374505_-|plate	baseplate J/gp47 family protein	A0A0C5AEG2	Bacteriophage	2.7e-113	55.9
WP_042217874.1|7374508_7374838_-	GPW/gp25 family protein	NA	NA	NA	NA
WP_042220130.1|7374834_7375233_-|tail	phage tail protein	A0A0C5AN08	Bacteriophage	5.4e-32	48.0
WP_052429719.1|7375258_7375696_-|plate	phage baseplate assembly protein V	NA	NA	NA	NA
WP_042217877.1|7375689_7376721_-	phage late control protein	A0A0C5AJ59	Bacteriophage	1.5e-105	52.5
WP_042217879.1|7376726_7376927_-|tail	tail protein X	Q6QIA3	Burkholderia_phage	2.8e-05	38.1
WP_042217881.1|7376923_7379884_-|tail	phage tail tape measure protein	M4ZR40	Bacillus_phage	1.8e-18	33.3
WP_042217882.1|7380033_7380354_-|tail	phage tail assembly protein	A0A0C5AEP1	Bacteriophage	2.4e-14	47.5
WP_042217884.1|7380366_7380885_-|tail	phage major tail tube protein	A0A0C5AJ56	Bacteriophage	4.0e-35	44.8
WP_042217886.1|7380898_7382344_-|tail	phage tail sheath family protein	A0A0C5AEE8	Bacteriophage	5.0e-136	52.2
WP_042217888.1|7382347_7382632_-	hypothetical protein	NA	NA	NA	NA
WP_042217889.1|7382628_7383051_-	hypothetical protein	NA	NA	NA	NA
WP_042220131.1|7383226_7383700_-	hypothetical protein	A0A0K2CNQ1	Brevibacillus_phage	4.3e-28	46.2
WP_052429720.1|7383950_7384349_+	helix-turn-helix transcriptional regulator	R9TNF4	Paenibacillus_phage	1.7e-17	65.6
WP_052429721.1|7384435_7385332_+	ImmA/IrrE family metallo-endopeptidase	A0A2H4JA43	uncultured_Caudovirales_phage	6.7e-14	29.8
WP_042140127.1|7385490_7385883_-	30S ribosomal protein S9	NA	NA	NA	NA
WP_042140128.1|7385903_7386341_-	50S ribosomal protein L13	NA	NA	NA	NA
WP_042217891.1|7386574_7387354_-|tRNA	tRNA pseudouridine(38-40) synthase TruA	NA	NA	NA	NA