CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP033687	Bacillus coagulans strain DSM 2314 chromosome, complete genome	14 crisprs	csf3gr5,csf2gr7,csf1gr8,RT,cas2,cas1,cas4,cas7,cas8c,cas5,cas3,csa3,DinG,casR,DEDDh	13	30	10	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP033687_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_1

237638-237709

Orphan

Consensus_repeat	Method
CCTATTTCAATTCCTTCTTCCTTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_1

>merge|NZ_CP033687|1|237638-237709|CRISPRCasFinder
CCTTTTTCAATCCCTATTTCAATTCCTTCTTCCTTCCCCTTTTCAATCCCTTTTTCAATCCCTTTTTCTATT

>NZ_CP033687|1|1|237638-237709|CRISPRCasFinder
CCTTTTTCAATCCCTATTTCAATT	CCTTCTTCCTTCCCCTTTTCAATC
CCTTTTTCAATCCCTTTTTCTATT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_017551796.1\|232146_233127_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224196
NZ_CP033687.1\|WP_080952280.1\|239078_239777_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP033687.1\|WP_110134135.1\|231494_232028_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|180687
NZ_CP033687.1\|WP_026684938.1\|242239_242767_+\|folate-family-ECF-transporter-S-component	unknown	unknown	gnl\|CDD\|275311
NZ_CP033687.1\|WP_017551799.1\|229920_230658_+\|pyruvate-formate-lyase-activating-protein	unknown	unknown	gnl\|CDD\|131546
NZ_CP033687.1\|WP_014097414.1\|233123_234035_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP033687.1\|WP_061086854.1\|239776_241135_+\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|274368
NZ_CP033687.1\|WP_014097407.1\|241314_241947_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014097412.1\|235255_235486_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_110134137.1\|243044_244355_+\|transposase	unknown	unknown	gnl\|CDD\|379382
NZ_CP033687.1\|WP_035200606.1\|247091_247967_-\|YitT-family-protein	unknown	unknown	gnl\|CDD\|224203
NZ_CP033687.1\|WP_061577681.1\|245616_246273_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_017551801.1\|226027_227188_-\|iron-containing-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|341467
NZ_CP033687.1\|WP_014097411.1\|236122_237103_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_081092962.1\|227566_229831_+\|formate-C-acetyltransferase	unknown	unknown	gnl\|CDD\|153087
NZ_CP033687.1\|WP_110134138.1\|244877_245660_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP033687.1\|WP_110134136.1\|234031_234835_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|239947
NZ_CP033687.1\|WP_035183918.1\|248080_248545_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224759
NZ_CP033687.1\|WP_017551798.1\|230918_231476_-\|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|377026
NZ_CP033687.1\|WP_052042183.1\|244696_244888_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213197

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_017551796.1\|232146_233127_-\|ABC-transporter-permease	gnl\|CDD\|224196	COG1277, NosY, ABC-type transport system involved in multi-copper enzyme maturation, permease component [General function prediction only].	3.33947e-19
NZ_CP033687.1\|WP_080952280.1\|239078_239777_+\|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].	9.74738e-85
NZ_CP033687.1\|WP_110134135.1\|231494_232028_-\|hypothetical-protein	gnl\|CDD\|180687	PRK06770, PRK06770, hypothetical protein; Provisional.	1.29648e-27
NZ_CP033687.1\|WP_026684938.1\|242239_242767_+\|folate-family-ECF-transporter-S-component	gnl\|CDD\|275311	TIGR04518, conserved_hypothetical_protein, ECF transporter S component, folate family. Members of this model are the multiple membrane-spanning S (specificity) component of ECF (energy coupling factor) type uptake transporters. All seed members were found in the vicinity of the bifunctional enzyme folC, involved in making active cofactor from imported folate. However, some species have multiple members of this family, suggesting some diversity of function. [Transport and binding proteins, Unknown substrate].	1.69599e-34
NZ_CP033687.1\|WP_017551799.1\|229920_230658_+\|pyruvate-formate-lyase-activating-protein	gnl\|CDD\|131546	TIGR02493, PFLA, pyruvate formate-lyase 1-activating enzyme. An iron-sulfur protein with a radical-SAM domain (pfam04055). A single glycine residue in EC 2.3.1.54, formate C-acetyltransferase (formate-pyruvate lyase), is oxidized to the corresponding radical by transfer of H from its CH2 to AdoMet with concomitant cleavage of the latter. The reaction requires Fe2+. The first stage is reduction of the AdoMet to give methionine and the 5'-deoxyadenosin-5-yl radical, which then abstracts a hydrogen radical from the glycine residue. [Energy metabolism, Anaerobic, Protein fate, Protein modification and repair].	9.76004e-127
NZ_CP033687.1\|WP_014097414.1\|233123_234035_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.33179e-105
NZ_CP033687.1\|WP_061086854.1\|239776_241135_+\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	1.08654e-57
NZ_CP033687.1\|WP_110134138.1\|244877_245660_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.53597e-44
NZ_CP033687.1\|WP_110134137.1\|243044_244355_+\|transposase	gnl\|CDD\|379382	pfam13808, DDE_Tnp_1_assoc, DDE_Tnp_1-associated. This domain is frequently found N-terminal to the transposase, IS family DDE_Tnp_1, pfam01609 and its relatives.	2.0389e-09
NZ_CP033687.1\|WP_035200606.1\|247091_247967_-\|YitT-family-protein	gnl\|CDD\|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	1.18921e-70
NZ_CP033687.1\|WP_017551801.1\|226027_227188_-\|iron-containing-alcohol-dehydrogenase	gnl\|CDD\|341467	cd08188, PDDH, 1,3-Propanediol (1,3-PD) dehydrogenase. This family includes 1,3-propanediol (1,3-PD) dehydrogenase, a key enzyme in the microbial production of 1,3-PD that has been previously characterized as the product of dhaT gene in Klebsiella pneumoniae. 1,3-PD dehydrogenase is a member of the family III metal-dependent polyol dehydrogenases, which are shown to require a divalent metal ion for catalysis. However, some members of this family showed a dependence on Fe(2+) or Zn(2+) for activity.	0
NZ_CP033687.1\|WP_081092962.1\|227566_229831_+\|formate-C-acetyltransferase	gnl\|CDD\|153087	cd01678, PFL1, Pyruvate formate lyase 1. Pyruvate formate lyase catalyzes a key step in anaerobic glycolysis, the conversion of pyruvate and CoenzymeA to formate and acetylCoA. The PFL mechanism involves an unusual radical cleavage of pyruvate in which two cysteines and one glycine form radicals that are required for catalysis. PFL has a ten-stranded alpha/beta barrel domain that is structurally similar to those of all three ribonucleotide reductase (RNR) classes as well as benzylsuccinate synthase and B12-independent glycerol dehydratase.	0
NZ_CP033687.1\|WP_110134136.1\|234031_234835_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|239947	cd04506, SGNH_hydrolase_YpmR_like, Members of the SGNH-hydrolase superfamily, a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid. This subfamily contains sequences similar to Bacillus YpmR.	1.2089e-70
NZ_CP033687.1\|WP_035183918.1\|248080_248545_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.88226e-15
NZ_CP033687.1\|WP_017551798.1\|230918_231476_-\|NAD(P)H-dependent-oxidoreductase	gnl\|CDD\|377026	pfam03358, FMN_red, NADPH-dependent FMN reductase.	5.36242e-30
NZ_CP033687.1\|WP_052042183.1\|244696_244888_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213197	cd03230, ABC_DR_subfamily_A, ATP-binding cassette domain of the drug resistance transporter and related proteins, subfamily A. This family of ATP-binding proteins belongs to a multi-subunit transporter involved in drug resistance (BcrA and DrrA), nodulation, lipid transport, and lantibiotic immunity. In bacteria and archaea, these transporters usually include an ATP-binding protein and one or two integral membrane proteins. Eukaryotic systems of the ABCA subfamily display ABC domains that are quite similar to this family. The ATP-binding domain shows the highest similarity between all members of the ABC transporter family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	1.39804e-19

>NZ_CP033687.1|WP_014097411.1|236122_237103_+|hypothetical-protein
MLNTHNDIKQTYYAEIKEKKISSYGAYAKKGKGVKHEIGKIYFASDLLRGKEKKLYKKSGKVKVYNMFTSLMTYEDLKSHPKERQTEILTKWRETYSENEIIEALGVEEEVYYQLLTDLGLEMKKKRTIPHSKPDADPNQVIPFNDLKKLPKKDQWLLISEYTEKWNAQSIAKIWGKRDSSVHNYKHNLKKLALKNGWIDEYKKDKAQENIKDFTPAAVESGQEPAGNAGDERVDQLMSEFKEMKMLINNLLSSNNQVAVEETEKIAERDATENEENNEKPESFTMNYENETEGFIIFQDLKRFIAVLEKNPDRFKVEVKLTRIEE
>NZ_CP033687.1|WP_014097412.1|235255_235486_-|hypothetical-protein
MLLFFGKFILLYLFLSIAFALFKVLYYNIGKKFVSKTADGTILHWALSVFVKNGTKMDSNDYFVMAVLAALFAIYL
>NZ_CP033687.1|WP_110134136.1|234031_234835_-|SGNH/GDSL-hydrolase-family-protein
MKKHLISAISIVSAVSALLFLAGLWMVFEDQQTKATGVKTETARTGNNTSKAGGTKQITITAIGDSLTRGTGDTAGKGYAGYVADRLKKKTKKAVLLQNNGIKGLTSSGLLEQLKQPQIKRELKSADIILLTIGGNDLFAGGEALDHLNTAYIEKLEKPYLANLKQIYAGIRAVNKTAIVYHVGLYNPFIDLSEAKTTSAIVRKWNFDSASVASDFPKVIYVPTFDLFEQNVNDYLYSDKFHPNTAGYQLIGERVASLIHYREEKAK
>NZ_CP033687.1|WP_014097414.1|233123_234035_-|ABC-transporter-ATP-binding-protein
MTTIPALKVIDVHKKIGRKEIIKGISFEVMPGEVFGFLGPNGAGKTTTIRMLTGLIRPTSGKILIGGKNVRTEFTEAMKNLGCIVENPEMYPFLTGYENLAYFARMDPSIPRNRLDEVAALVGLTGRIHDKVKTYSLGMRQRLGIAQALLGNPKLLILDEPTNGLDPAGIREMREFIRSLAEKAHLSVLVSSHLLSEVQLMCDKVAIIHNGQVIRTGNVHELLSEKARTFWKVAPIEKARTLLQAETQVAEGEDGLLVTPYDEEKNALWNEMLVQNGVRVKEMKAVLPALEDLFLELTGGRKK
>NZ_CP033687.1|WP_017551796.1|232146_233127_-|ABC-transporter-permease
MIQLIYNEQLKLWKKKRILVIMLIIACLVPIFTYAQYKESKALQEKIGTTDWRVKLQKQIVDTQNRLGSASLSDDFKKYLRITLSQEQYYLNHNINPNAPGAPTFMRVFIENAIGMLLPLFVMVAASDIVSAEAGSGTIKLLLTRPVKRWRILLSKYIAMLLSVSFILLCTAVFTYGISGLVFGYHGWNMPILTGFTIKGDELLTSHVHAVSQWKYLLMAFGLAWFVGVVSGSLTFMLSVLLRSTAAVMGIMLSSLIAGAILTNMVSAWPSAKYLFMVNLQLTNYLNGTSPPVAGMTLGFSVAVLLVWLFLSLVVSFVVFTKRDVY
>NZ_CP033687.1|WP_110134135.1|231494_232028_-|hypothetical-protein
MFQRFVVGMGIAVFMFIAGVTYFYFNKGEAIATEAAPSKKPAAEEETAAKAVIQESFYQKTPERKLSAYKSMSEEALVQEVHNMTHQKVAANEKWGASEITKEKVDALYSAISNQTFADTELQDMLLGILKPWKKGDFSNAVKAHNEIWAYQKGNIGKAERRLTPSEEAAYIKENFK
>NZ_CP033687.1|WP_017551798.1|230918_231476_-|NAD(P)H-dependent-oxidoreductase
MKILGISGSLTGEKTSIGVYEVLMAIKAEDPEAETELLDLKDYEVEFARGFPLSYYNDDTIAAVNKMLEADILVFGSPIYQASITGALKNLLDHLHRDAFQSKVCGIVMNGGSDKHFLVAEYQLKPVLTFLKATCAVRNVFIHNDDFNEDNEIINADIQARIRKLAHELLQLRKAFSGGNPGNLG
>NZ_CP033687.1|WP_017551799.1|229920_230658_+|pyruvate-formate-lyase-activating-protein
MNMTTRIHSTESFGTVDGPGIRYVVFTQGCPLRCKFCHNPDTWKINEGNEMSVEEIMSDVRDYLPFIEASGGGITVSGGEPLLHLDFLIELFKACKEIGVHTAIDTAGGCFSRSSRFMEKLDELMKYTNLVLLDIKHIDPEKHKWLTGMSNEHILDFARYLADKHIPVWIRHVLVPGVDSEEDLQKTSDFIHSLPNVEKIEILPYHKLGVYKYEALGIDYPLKGVEPPTKEQVAHAEQILKRELQ
>NZ_CP033687.1|WP_081092962.1|227566_229831_+|formate-C-acetyltransferase
MTEQLLTKATLSKKQWEGFKGGNWQKEIDVRDFILKNVTPYEGDESFLAGPTEATLKLWDQVMELSKQEREKGGVLDMDTKIVSTITSHGPGYLNKELEKIVGFQTDKPFKRSMMPFGGIRMAESALKSYGYEIDPEIKHIFTEWRKTHNQGVFDAYTPEIKAARHAGIVTGLPDAYGRGRIIGDYRRVALYGVDYLIEQKKKDLDLIGCGLMTEEVIREREEHSEQIRALQELKQMAQSYGFDISEPASNAHEAFQWLYFAYLAAIKEQNGAAMSLGRTSTFLDIYIERDLKNGVLTEREAQELVDHFVMKLRLVKFARTEDYNELFSGDPTWVTESIGGMALDGRTLVTKNSFRFLNTLDNLGPAPEPNLTVLWSTKLPDKWKQYCAKMSIKTSAIQYENDDLMREEYGDDYGIACCVSAMRIGKQMQFFGARANLAKALLYAINGGVDERYKMQVAPPFQPITSEYLNYDEVMEKYDRMLDWLAGVYINALNIIHYMHDKYSYERLEMALHDRNVLRTMACGVAGLSVAADSLSAIKYAKVKVIRDEDGLAVDYEVEGDYPKYGNNDDRVDQIAVNLVKSFMQKLQKYPTYRNAVHTSSILTITSNVVYGKKTGSTPDGRKAGEPFAPGANPMHGRDSHGAVASLTSVAKLPYKYSLDGISNTFSIVPEALGHEEETQVSNLDGMLDGYMAKKAHHLNVNVLHRETLLDAMDHPEKYPQLTIRVSGYAVNFIKLTREQQLEVINRTFHEMM
>NZ_CP033687.1|WP_017551801.1|226027_227188_-|iron-containing-alcohol-dehydrogenase
MLTGLRTDFQMPSVNLFGQGTAEEIGNRLKNLGCRRPLIVTDEGLHQLGYSEKIAAYIKEAGLEVAIYPKAEPNPTDKNVEDGLKTYHEENCDSIVSLGGGSAHDCAKGIGLVAANGGKIHDYEGLDRSEKPMVPLVAINTTAGTASEMTKFTIITDTSRKVKMAIVDKHVTPVLSINDPLLMVGMPPSLTAATGLDALTHAVEAYVSTAATPVTDACAIKAIQIIPQYLPKAVANGNDMEAREQMVYAQYLAGMAFNNASLGYVHAIAHQFGGFYNLPHGVCNAILLPHVCRFNLIARKERFAEIAVALGEKTDGLSVDEAAEKAITAIERLAAQLNIPKGFKELGAKEEDIEILAQHAMQDACAATNPRKPTQKEVEAIIKAAM
>NZ_CP033687.1|WP_080952280.1|239078_239777_+|response-regulator-transcription-factor
MSKIMIVEDDVKIARVLELELQHEHYDTVWVENGSQALNLLESEDWDLVLLDVMIPGLSGLEVLRRYRMRNSRTPVILLTARNSVLDKVNGLDHGANDYITKPFNIEELLARIRAALRTGALHTGKSENSKKHEYALADLLVNTATRQVTRGGKPIELTKREFDLLCYLLKNKRIVLNREQLLNEVWGFEYAGDTNVVDVYIGYLRKKIDHGHETALIHTVRGVGYTMKETG
>NZ_CP033687.1|WP_061086854.1|239776_241135_+|HAMP-domain-containing-histidine-kinase
MSIKKKLSALLILWSFIVLFAGNTIVFLAFLYFSKDRLETSLENSAEQLAESVGSGDALFSDPEPILQTHVPDEGMIRLFNAQHQKIYVKADEEDLLSIKPVFPKDDQTRTVKGEDFTAIVASYPIMENGKYLGMLELSVVPEDIFEDSRLLLTILLASSAVLIVLAAFVGVKTSGLFLKPVSTMMKTMADIEENGRFEKIPLALNHHDELYQMALTFNAMIDRLEAMFKKQEQFIYDASHELKTPLTVIESYAAMLRRWGKDDPEILAEGIAAISDESRRLNSIAEQLLALARSEDVSYELQPVDAANLCRQTAKRLSQSSNRSISVKAETPGLYAWTNEEKFVQVLVILLDNALKYSRFPVQIEVGSDNDFVTVTVIDHGTGIPKEDLPHLFERFYRVDKARTRGTGGTGLGLSIAHSIMTQHGGGIKIESEEGKGTRVCLQFKKVVDAS
>NZ_CP033687.1|WP_014097407.1|241314_241947_-|hypothetical-protein
MKWIKVLIGVIVLSVAGGAGIAVGMNMKEERPVVYSDPAETISAPEAKKEEPVASYTVNKEGGQSKTANPVIRETEGKVTALDKQSITVSFPFGGSETFKLTNQTVVEDFSLPLKKGVLVELKASGEEAVKIETERTMDVKAVIVSDEKESMKVEANGTTKSFTKGHFYRLDRDGYRGSLKGVPVELDLDEHDKILSAELDDEFLDGYDD
>NZ_CP033687.1|WP_026684938.1|242239_242767_+|folate-family-ECF-transporter-S-component
MNVKKIVFAGLFIALEVIFTRFLSIQTPIIRIGFTFIPTALSAVLLGPLFAGITAGLADIIGMVLFSGGAAYFPGFTLSAFLSGAIYGLFLYRKSVRFWRVCMAVLIITVVVNLGLDTLWLWMLTGKGILGLLPARFIKSVIMFPIQVILIQVVWKSLAVSLRLEPSHHFPNGFR
>NZ_CP033687.1|WP_110134137.1|243044_244355_+|transposase
MVTRKEKRNREKEANYFFEFLKIQKHFFRDLMNNLKKVADHRHQSYITYGPEVLLFTMMLKNMTGLKSMRNMSESFNKEECIKNVGKVLGLDSLEELPHYDTINDFLSGLDVNELEKIRTYMIKELLKKRSLESYRIEGKYWGVIIDGTGLHTFHEKHCKHCLRRAYTNKETGETNVLYMHHVLEAKLVVGDMVFSIASEFIENESENVSKQDCELKAFDRLAKKIKKIFKRLPICILGDSLYACETVFNLCRAHKWKYICRFKEGRIKSISTEFKAIKELEQSKDQNSLVWVNDIAYKDRTVNLMEATMKTEDGKSKEYVFITDIKITKKNVERLIAAGRSRWKIENQGFNEQKNNRYNIEHANSQNYTAMKNHYLLVQITDIIRQLFEKGSSILKALKKTAKEKSSNLLESFRTRILTDEDFTHLSKPIQVRFT
>NZ_CP033687.1|WP_052042183.1|244696_244888_+|ATP-binding-cassette-domain-containing-protein
MGEIIKFNHVTKMYKKTTALHNLSFSIDSNEIVGLLGPNGAGKTTIIKLIAYLNLSYKGRNIN
>NZ_CP033687.1|WP_110134138.1|244877_245660_+|ABC-transporter-ATP-binding-protein
MLINEKVNKKKNPIISCIMEGNRNLYWKLTVKENIEFFLALKGINYKTKKEQIETLIDEFELGSKRNELVQNLSRGMQQKLSILIALLEDSQIILLDEPTLGLDVSTLRDLEELIPKIPSQMNKSLVITSHNMRFVEKVCNKILIIRKGQLIAEKTIDEFKNMVDTKLGTVRVKDLNGLEAELKEHSIPFTEEKIKYIISFKNVSQFIEILDLCKENGEIIDFHYGQLEFEDLFLKIINDSEGGQIVADESIHKERSHSS
>NZ_CP033687.1|WP_061577681.1|245616_246273_+|hypothetical-protein
MLMKAYIKKEAILAKRYLANSIGGGITIFLVFLLIFYGYSGIVGFNLGSDTKESLILSFTIWILALSIYQNITDSIEEETQIGTIEQLYLSRYSFLFVITVKSIAMLVIDFVQIIVLLLLMMIVTQTFLNFQNILSIIFVTFFVSLNYWGLGYALAGGVLLYKKMSTYLQIMQFVLLGLMFIPAESHTLFKLIPSVWGLKLLKDIMVSNTSIITFSMI
>NZ_CP033687.1|WP_035200606.1|247091_247967_-|YitT-family-protein
MNTTTKKKRTIRLKKVSRALAVMIGAFIAAYGLETVLIPNNVSDGGVTGLSIVGSQLSGLPLGLLIVVINIPFVFLGYKQIGKSFAIYSMIGIASLAIGTRLMRPLPAIIQGDTMIITVVGGIIIGFGMGLALRNGGALDGIDMLAVLLSRKLPFGSSDLILFLNMFVFIIVAIVFGLQGAILSAIVYFIASKVIHIVEEGLSGSKTFKIITDQPELMVETIRDRLGRSATYNLVEGGYSNEQFKEITCVINRLEDSKIKEIIYEIDKHAFVTVYDVSEVRGGNFKKRNIH
>NZ_CP033687.1|WP_035183918.1|248080_248545_-|MarR-family-transcriptional-regulator
MDLNYDDPKVKQAMEIYQLLTAIGKFTAKLAKKNAENFGLSLQQLSILNTLLAFPESTQQELAERLVLSKSTISVGIDKLVNMGLIERKLSTEDRREVKLQLTLKGEELAKKSSKNAIPYQAMIYAIEKMPEEDIQSLLRIQQELLNHLNEYGY

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Crispr_ID: NZ_CP033687_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_2

313529-313620

Orphan

Consensus_repeat	Method
CAAATAATTACCTGTTTAAGAAGAAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_2

>merge|NZ_CP033687|2|313529-313620|CRISPRCasFinder
CAAATAATTACCTGTTTAAGAAGAACTTACGCTAGTGGGAATGGCAATATCTGCATACTTTTGGCACAAATAATTACCTGTTTAAGAAAAAC

>NZ_CP033687|2|2|313529-313620|CRISPRCasFinder
CAAATAATTACCTGTTTAAGAAGAAC	TTACGCTAGTGGGAATGGCAATATCTGCATACTTTTGGCA
CAAATAATTACCTGTTTAAGAAAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_035183866.1\|312212_312530_-\|YfhH-family-protein	unknown	unknown	gnl\|CDD\|378063
NZ_CP033687.1\|WP_014097366.1\|304053_305511_+\|glutamate-synthase-subunit-beta	unknown	unknown	gnl\|CDD\|237213
NZ_CP033687.1\|WP_014097362.1\|307805_307964_-\|small,-acid-soluble-spore-protein-K	unknown	unknown	gnl\|CDD\|285399
NZ_CP033687.1\|WP_110134147.1\|306010_306622_-\|ABC-2-transporter-permease	unknown	unknown	gnl\|CDD\|379133
NZ_CP033687.1\|WP_110134151.1\|319500_320883_-\|anthranilate-synthase-component-I	unknown	unknown	gnl\|CDD\|237431
NZ_CP033687.1\|WP_061086973.1\|305641_305950_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|290824
NZ_CP033687.1\|WP_017551428.1\|321864_323046_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|182528
NZ_CP033687.1\|WP_035190007.1\|306599_307475_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP033687.1\|WP_110134149.1\|315303_316509_-\|tryptophan-synthase-subunit-beta	unknown	unknown	gnl\|CDD\|235288
NZ_CP033687.1\|WP_014097361.1\|308050_309031_-\|metal-dependent-hydrolase	unknown	unknown	gnl\|CDD\|224899
NZ_CP033687.1\|WP_017551423.1\|317911_318937_-\|anthranilate-phosphoribosyltransferase	unknown	unknown	gnl\|CDD\|234682
NZ_CP033687.1\|WP_014097348.1\|323042_323726_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224059
NZ_CP033687.1\|WP_026684724.1\|309209_310328_+\|A/G-specific-adenine-glycosylase	unknown	unknown	gnl\|CDD\|224115
NZ_CP033687.1\|WP_017551419.1\|313681_313864_+\|YfhD-family-protein	unknown	unknown	gnl\|CDD\|372930
NZ_CP033687.1\|WP_014097355.1\|314122_314914_-\|tryptophan-synthase-subunit-alpha	unknown	unknown	gnl\|CDD\|237285
NZ_CP033687.1\|WP_017551424.1\|318920_319520_-\|aminodeoxychorismate/anthranilate-synthase-component-II	unknown	unknown	gnl\|CDD\|235552
NZ_CP033687.1\|WP_110134146.1\|299204_303770_+\|glutamate-synthase-large-subunit	unknown	unknown	gnl\|CDD\|236968
NZ_CP033687.1\|WP_110134148.1\|314906_315311_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|183851
NZ_CP033687.1\|WP_110134150.1\|316486_317911_-\|bifunctional-indole-3-glycerol-phosphate-synthase-TrpC/phosphoribosylanthranilate-isomerase-TrpF	unknown	unknown	gnl\|CDD\|236509
NZ_CP033687.1\|WP_014097358.1\|312510_313326_-\|recombination-regulator-RecX	unknown	unknown	gnl\|CDD\|237619

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_035183866.1\|312212_312530_-\|YfhH-family-protein	gnl\|CDD\|378063	pfam08838, DUF1811, Protein of unknown function (DUF1811). This is a bacterial family of uncharacterized proteins. Some of the proteins are annotated as being transcriptional regulators. The structure of one of the proteins in this family has revealed a beta-barrel like structure with helix-turn-helix like motif.	4.50683e-59
NZ_CP033687.1\|WP_014097366.1\|304053_305511_+\|glutamate-synthase-subunit-beta	gnl\|CDD\|237213	PRK12810, gltD, glutamate synthase subunit beta; Reviewed.	0
NZ_CP033687.1\|WP_014097362.1\|307805_307964_-\|small,-acid-soluble-spore-protein-K	gnl\|CDD\|285399	pfam08176, SspK, Small acid-soluble spore protein K family. This family consists of the small acid-soluble spore proteins (SASP) belonging to the K type (sspK). The sspK are unique to the spores of Bacillus subtilis and are expressed only in the forespore compartment of sporulating cells of this organism. The sspK gene is monocistronic and transcription is primarily by the RNA polymerase with the forespore-specific sigma factor, sigma-G. Mutation deleting sspK results in loss of SspK from the spore but had no discernible effect on sporulation, spore properties or spore germination.	6.9293e-19
NZ_CP033687.1\|WP_110134147.1\|306010_306622_-\|ABC-2-transporter-permease	gnl\|CDD\|379133	pfam13346, ABC2_membrane_5, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family pfam01061.	6.4582e-12
NZ_CP033687.1\|WP_110134151.1\|319500_320883_-\|anthranilate-synthase-component-I	gnl\|CDD\|237431	PRK13570, PRK13570, anthranilate synthase component I; Provisional.	0
NZ_CP033687.1\|WP_061086973.1\|305641_305950_-\|hypothetical-protein	gnl\|CDD\|290824	pfam14118, YfzA, YfzA-like protein. The YfzA-like protein family includes the B. subtilis YfzA protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 100 amino acids in length.	0.000424361
NZ_CP033687.1\|WP_017551428.1\|321864_323046_-\|FtsX-like-permease-family-protein	gnl\|CDD\|182528	PRK10535, PRK10535, macrolide ABC transporter ATP-binding protein/permease MacB.	3.00621e-44
NZ_CP033687.1\|WP_035190007.1\|306599_307475_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.14905e-68
NZ_CP033687.1\|WP_110134149.1\|315303_316509_-\|tryptophan-synthase-subunit-beta	gnl\|CDD\|235288	PRK04346, PRK04346, tryptophan synthase subunit beta; Validated.	0
NZ_CP033687.1\|WP_014097361.1\|308050_309031_-\|metal-dependent-hydrolase	gnl\|CDD\|224899	COG1988, COG1988, Predicted membrane-bound metal-dependent hydrolases [General function prediction only].	2.963e-38
NZ_CP033687.1\|WP_017551423.1\|317911_318937_-\|anthranilate-phosphoribosyltransferase	gnl\|CDD\|234682	PRK00188, trpD, anthranilate phosphoribosyltransferase; Provisional.	1.74848e-172
NZ_CP033687.1\|WP_014097348.1\|323042_323726_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224059	COG1136, SalX, ABC-type antimicrobial peptide transport system, ATPase component [Defense mechanisms].	1.00169e-102
NZ_CP033687.1\|WP_026684724.1\|309209_310328_+\|A/G-specific-adenine-glycosylase	gnl\|CDD\|224115	COG1194, MutY, A/G-specific DNA glycosylase [DNA replication, recombination, and repair].	9.39498e-155
NZ_CP033687.1\|WP_017551419.1\|313681_313864_+\|YfhD-family-protein	gnl\|CDD\|372930	pfam14151, YfhD, YfhD-like protein. The YfhD-like protein family includes the B. subtilis YfhD protein, which is functionally uncharacterized. Its expression is regulated by the sporulation-specific sigma factor sigma-F. This family of proteins is found in bacteria. Proteins in this family are approximately 50 amino acids in length. There is a single completely conserved residue E that may be functionally important.	3.32724e-18
NZ_CP033687.1\|WP_014097355.1\|314122_314914_-\|tryptophan-synthase-subunit-alpha	gnl\|CDD\|237285	PRK13111, trpA, tryptophan synthase subunit alpha; Provisional.	2.89155e-111
NZ_CP033687.1\|WP_017551424.1\|318920_319520_-\|aminodeoxychorismate/anthranilate-synthase-component-II	gnl\|CDD\|235552	PRK05670, PRK05670, anthranilate synthase component II; Provisional.	7.6178e-120
NZ_CP033687.1\|WP_110134146.1\|299204_303770_+\|glutamate-synthase-large-subunit	gnl\|CDD\|236968	PRK11750, gltB, glutamate synthase subunit alpha; Provisional.	0
NZ_CP033687.1\|WP_110134148.1\|314906_315311_-\|hypothetical-protein	gnl\|CDD\|183851	PRK13028, PRK13028, tryptophan synthase subunit beta; Provisional.	0.00315582
NZ_CP033687.1\|WP_110134150.1\|316486_317911_-\|bifunctional-indole-3-glycerol-phosphate-synthase-TrpC/phosphoribosylanthranilate-isomerase-TrpF	gnl\|CDD\|236509	PRK09427, PRK09427, bifunctional indole-3-glycerol-phosphate synthase TrpC/phosphoribosylanthranilate isomerase TrpF.	3.06789e-132
NZ_CP033687.1\|WP_014097358.1\|312510_313326_-\|recombination-regulator-RecX	gnl\|CDD\|237619	PRK14135, recX, recombination regulator RecX; Provisional.	3.50701e-115

>NZ_CP033687.1|WP_014097358.1|312510_313326_-|recombination-regulator-RecX
MPVITKISVQKNNKERYNIFLDGQYRFSVDEEVLARYQLLKGKELDELDIEAILAEDDIRKGVNTAIHFLSYRMRSEKEVRDDLIKKEFAPEVIRSVISKLYELQYLDDAEFAASFVRTQMNTTHKGPVVIRRELQQKGIAPELVKKALEIFDADQQVEHALALAEKLSRQHARLSEKLLKQKVEQGLVVKGYPPEVISAAMAALHIEKDEEAEWEALLQHAEKAKRKYGRLSGYAYRQKMKQFLYRKGFPVDLIDRYLREEEDGDGKKIQ
>NZ_CP033687.1|WP_035183866.1|312212_312530_-|YfhH-family-protein
MEKRYSEMSEYELKQEIAQLTEKARKAEQLGIVNEFAVLERKIAMAKSYLLDPASFQKGEIYEIEGDPGVYFKIDYIDGVFAWGYRVSGGKPIEALPISMLKQVD
>NZ_CP033687.1|WP_026684724.1|309209_310328_+|A/G-specific-adenine-glycosylase
MKNLPIDDFDIKSFQDDLISWFEREQRKLPWREDRDPYKIWVSEIMLQQTRVDTVIPYFRRFMEKFPTIEALADASEDEVLKAWEGLGYYSRVRNLHAAVKEVEEHYGGTVPDTPEEVSKLKGVGPYTAGAILSIAYGLPEPAVDGNVMRVLARILSIWEDIAKPSARKVFEEVVRKLISRENPSFFNQALMELGALVCTPKSPSCLLCPVREHCRAFREGTIDELPVKSKGKKQKQIRLQAAVLEDEDGRILIHKRPDKGLLANMWEFVQVEESTVLPARQVLKDYLGDVFKIEAALETEHFTEIRHVFTHLIWDIRVYHGKILNQVQETNELKCVPPDEIETFAFPVPHQKIWKAFREQAKSEKVKDIKG
>NZ_CP033687.1|WP_014097361.1|308050_309031_-|metal-dependent-hydrolase
MDTGTHVVMGFALGGLATLDPVVAQDAVHFHSVLIATVLGSQAPDIDTLLKFKNNAVYIRNHRGITHSVPAVLLWPLAITAVLSIFFPGTDALHLWLWSFLAVFLHVFVDIFNAYGTQALRPFSYKWVALGVINTFDPFIFTIHVIGIAAWLFGAQPGPTFLAMYIFIFLYYIARFAARHDVKKAVLARIPDAENIIISPTVRFHQWKIAVRTKDAYYVASAFKSAVTILDKFKRLPVPENEIIEAAKQDKNLSAFLSFSPVYNWQVKELDNGWEVRFTDLRYRKNGHYPFVAVVKLNEDLEITGSYTGWIFNKKKLKKKLDVVPR
>NZ_CP033687.1|WP_014097362.1|307805_307964_-|small,-acid-soluble-spore-protein-K
MRNKEKGFPYHHDNVYEGKPRAKAEYASKRADGTTNTHPQERMHASGRRGES
>NZ_CP033687.1|WP_035190007.1|306599_307475_-|ABC-transporter-ATP-binding-protein
MEYALEIEGLCKSFSKSRFALKNISFSVPYGSITGFIGENGAGKTSTMGAILQTLHIDSGSIKIFGERIAEAKKEINNHIGVVYDAMNFSGNLDAIKLSKVFRYLYHNWDNQEYFNYIELFSLPKKQKINSFSRGMAMKLSIAVALSHGARLLILDEATSGLDPVGREDVLEALLKFVRDQKGAILLSSHITSDIEKVADTLVFIKKGEIVLKTSKNDLLNNYAIIQCKEHELNDLRLNGIIAYKNQTDYVDVLVSNKNELPAKFHKKNFSIDDITLLLMKGENYERTHFK
>NZ_CP033687.1|WP_110134147.1|306010_306622_-|ABC-2-transporter-permease
MKGLILNNLYSIDKSVKFSLLISTAAIIPLIISGNPTALKIAVLLPFLIIPMNAFEVLKQDSMSSWNKFEITLPLKKSKIIQSKFITFLLLLFTSLLLTFALFYCASIFISPTVMDDFFNIGLRGMGLMFCAASLVYPLTYIFGIEKSDMITMGSMGFSFVMFFFISFLMKVFIGEMKGVEEIFSLSFLLVSIFYSFSHTLPR
>NZ_CP033687.1|WP_061086973.1|305641_305950_-|hypothetical-protein
MAKAVKNGHAKAAKKRYGWYIHLLIFVVAQLVFFIFDNVSASKNIFNLNDYGKWAVSALSPIYDWLQIYKSPQFNLIFVIWGAIFIIDGLIRMLPKRHSYSQ
>NZ_CP033687.1|WP_014097366.1|304053_305511_+|glutamate-synthase-subunit-beta
MRGTTDFIEQKREKPKELDAAKRVATWKEYVQAFPEAKLRTQASRCMECGTPFCQMGELIGRQTSGCPLYNLIPEWNTLAAQGKWEEAYQRLLLTNNFPEFTSRACPAPCEGSCTAGLVSEPVTIKSIERAIIDRAWEEGWIKPRIPLKRNGLKAAVVGSGPAGLTAADDLNQAGYDVTVFEKEDRFGGLLMYGIPNMKIEKQYVERRVDLLQAEGITFKANTEIGKDITLDELESAFDAVLLCIGAEKQRDMDIPGRDLKGIYPAMEYLKANTKHLLDHGENGEPQISAKGKKVIVIGGGDTGADCVATAIRQGCKSVVQFGKHGELPKERPEHEPWPVNPSLFTLDYAYEESFKVFGEDPRQYYIQTTAFHGNENGEVTGLVTVPFSDPRGAEQQVWEADLVLIAIGFQGVDDSKSAGIELQNGLIQTLPGSFQTNREGIFAAGDAKRGASLIVWAMQEGKKAAKEIDLYLSQKDKATCQPSA
>NZ_CP033687.1|WP_110134146.1|299204_303770_+|glutamate-synthase-large-subunit
MNNQHYGLYRPEFEHDACGIGFYADIKGRASHKIITTALEMLRRLDHRAGKNADGTTSDGAGISMQIPHAFFEAVCSFTLPKKGEYAVGMLFLPHDPHAAEDILNEFRIQAASLGLSVNGVREVPVNPEVLGRQAEESRPHIVQIFVSSSSNDNTEEAVFQRKIYILRKLVENKFGSSFYAASFSNRTIVYKGMLSAEQLPLFYIDLQDERFQSALALIHSRFSTNTFPSWERAHPNRMIAHNGEINTIKGNVNWFNAKIELFANELGLDTLKKIQPVINANGSDSAIFDNVLEFLTTNGISLPHAIMMMVPEPWEDNEDLPPYLKSFYEYHSQIMEPWDGPMALEFTNGKQIGAVLDRNGLRPARYYITHDDKIIFASEVGVVDVEPENVKERRHLKPGQLLFVDLEKGALIPSDELKAQVSLEKPYAEHLEDSVIDLEESHFIPAASSLEKNELAYRQTLFGYTYEECTKSIVPMAQEKNEPIGAMGVDTPIAVLSERPQLLFHYFKQSFSQVTNPPIDSIRESYVISTVTWLGPQVSLDGHDDTAHKKIRLEHPFLSTAKFNAILNQGMKTAFLPAYHSPDVTLEEALEQLLKEADEKIREGAEILILSDRAQGHRAVPIPSLLAVSALHQHMIRLGTRPKASIVLDSGEPRDSHHMAALLGYGADAVHPYLALETIQNLIDEGHIDLPYKKASENYLSTLKKSVVKIMSKVGITTMQSYRGAQTFEALGIAESVCDRYFTGTVSQLGGIGLAEIGQESLKRYEKAQELLFQHNKALDPGSELQWRKDGEYHLFNPQMMYTLQQAARTNNKELYRKFSETYHHGPYATIRSLLAIESNRKPVPLDEVEPVESIWKRFKTGAMSYGALSKEAHEALAIAMNRIGGKSNSGEGGEEKERYTPDANGDSRRSAIKQVASGRFGVTSLYLTDADEIQIKMAQGAKPGEGGQLPGSKVYPWIAEVRGSTPGVGLISPPPHHDIYSIEDLAQLIYDLKSANPRARISVKLVAKSGVGTIAAGVAKGLADTILISGHDGGTGASPQTSIKHAGMPWELGLAETHQTLTLNGLRNRVVLETDGKLMTGRDVVIAACLGAEEFGFSTAPLVVLGCIMMRACHLDTCPVGVATQNPKLRAKFMGKPEYVVNYMRFIAEEVREILAECGYRSLDELVGETGLLKVKDEVKNHWKAKQLHFDKLLFKADETPFAVQGKTVQNHKLEERFDSRELNHLSVSVRNRQQTAVTLSVRNTDRAIGTTLGHIITKTYGDEGLPEDFIHIHLHGSAGQSLGAFIPKGLTLNLEGDANDYVGKGLSGGKIVVKPGAGWIRDEEQAIIGNIAFFGATSGEAYIRGTAGQRFCVRNSGVHAVVEGIGDHGCEYMTGGRVAVLGSIGKNFAAGMSGGIAYIYTGAMGEDEVLARINQELVSIEGVDADEDMRELYHMIQKHYQYTGSPVAKRILKNWELSLHQFVKIVPREYKAMMELIQYFLDQQMPLDEARLAAFEYKKSGKHLPEIEKEKAFPTEVK
>NZ_CP033687.1|WP_017551419.1|313681_313864_+|YfhD-family-protein
MGRGHQHKTRDKNKATLPQVPKNMKIDGKDIEYSRELADGEDLEAQARSDAAAKRAKNSR
>NZ_CP033687.1|WP_014097355.1|314122_314914_-|tryptophan-synthase-subunit-alpha
MGKQKLEAQFETVLARGDQAFVPYIMAGDGGMEETEKRLAFLEACGATAIELGIPFSDPVADGPVIQAAGLRAFKAGTTMKKVLDHLKAHPRQVPIILMTYFNPVFAYGLEKFAADCANAGVDGLIIPDLPIEEEEEIAGELAKCGLALIRLAAITSPKDRLEEIASRSDGFLYAVTVTGTTGTRTNFHDNIEDYLDFLSSISRVPVLAGFGVSSPEQVRRLTRYCSGVVAGSKIIELFQHGETEKIRALVESAKQQAAPNQL
>NZ_CP033687.1|WP_110134148.1|314906_315311_-|hypothetical-protein
MGEIPALESTHGNSFALQSAKTIAASLLERRDKDGGAVSRLFGIGNIPALESIHGSSFALKPAKMVAASLLERRDKNEGAVSRLFGIGNIPALESIHGSSFALKPAKMVAASLLERRDKDEGAVSRLFGGENNG
>NZ_CP033687.1|WP_110134149.1|315303_316509_-|tryptophan-synthase-subunit-beta
MQTYKLPDTNGRFGTFGGRFVPETLMPAVNELEQAYHEAMNDPAFHAELEKLLKQYVGRETPLYFAENLTKLGGGPKIFLKREDLNHTGAHKINNTVGQALLTLRMGKKKVVAETGAGQHGVATATVCALLGLECMIFMGKEDIRRQKLNVFRMELLGAKVKSVAQGSGTLKDAVNEALRYWVAHVEDTHYIMGSAVGPHPFPQIVRDFQSVIGKETKKQIVEQTGKLPDAVVACVGGGSNSIGMFYPFVEDKSVKLFGVEAGGAGLGTGKHAASLSDGKLGVLHGMKTYLLQNDDGQIQEAYSVSAGLDYPGVGPEHSYLKETGRVTYTSVNDDEALDAFRLLSRTEGIIPALESAHAISFALKLAKTMGKDETIAVCLSGRGDKDVEAVSHLLGGENNG
>NZ_CP033687.1|WP_110134150.1|316486_317911_-|bifunctional-indole-3-glycerol-phosphate-synthase-TrpC/phosphoribosylanthranilate-isomerase-TrpF
MAFLEKILAEKEKEVARIKAAGKAFAPNARKAPSLYETFMHAEKTSIIAEIKRASPSKGDIRTGVDPIRQALAYEKAGAGAISVLTDEIFFKGSVEDLKAVSDAVRLPVLCKDFIIDEIQIDRAKAYGASVILLIAAALSPERLHQLYDYARGAGLEVLLEVHNEAELETAVEKGARIIGINNRNLKTFDVDLGVAEKLAPKISNPDVLVISESGIRTRKDVVRAEHAGAKGILVGETLMRANDPETAIKRLTGLPEKRKVKVCGIRTLEAARAAVSAGADMIGFVFAESKRKITPEKAVQIAEALPDHVEKVGVFVNESPEKMAEIAERAGLDYLQLHGDETAEDVAQIPYPVIKAFPVRTDADLEAIHVYRCDLVLLDSAGGKYRGGNGKAFDWELAKALSDERAVVLAGGLTPENVEAAILSARPHIVDVSSGVETNGEKDPDKIKAFVQATRKAFQKLEERDDNANIQTA
>NZ_CP033687.1|WP_017551423.1|317911_318937_-|anthranilate-phosphoribosyltransferase
MKPYLEKILAQEGLTFEEMREASRALFSDEVTEGEMGAFLAVLKSKGETAEEIAGLVEVIREKAVPVPCSVPGLMDNCGTGGDGSHSFNISSTSAFVLAASGVKVAKHGNRSVSSQTGSADVLEKLGISLSFPAEEIEGLLREIGIVFLFAPNVHPALGKMMKIRKDLRIPTIFNLIGPLTNPMNLETQLLGLYRRDMLRTMAEVLGRLGRKRALVVNGAGYLDEASLSGENHFALLDGGKITTFTLTPEQVGLPYYPLEAIHGGDAQKNSDILLSVLKGEKGAYRDTVLFNAGLALFAAGRAETVKEGIQIAEQAIESGAALEKLHALIEASRKLTQEAI
>NZ_CP033687.1|WP_017551424.1|318920_319520_-|aminodeoxychorismate/anthranilate-synthase-component-II
MILLLDNYDSFTYNLYQYFCELGEEVKVFRNDRITVDEIRRLKPEAIVLSPGPGVPENAGISIETVKTFYRQIPLLGVCLGHQAIAAAFGAGITKAKEIKHGKTSLVRHDGKGIFSGLPDPVEVMRYHSLVMDRTKIPEVLEVVAESLDDGEIMAIQHQSAPCFGVQFHPESIGTETGKQMLENFLREIRKDEKVETVS
>NZ_CP033687.1|WP_110134151.1|319500_320883_-|anthranilate-synthase-component-I
MQYKMVKLNGDVLTPIMIFKRLKGKCKFLFESSLPNDSNGRFSFIGADPVKAFIGRDDELEVIDRMTGRREIKKGKPLDIVKDLLPRLGIQLPFPFYGGAVGYIGYDAIRQYEEIGRVPEDETGIPDLHLMLYQNIAVYDHKSQTVYLVSTGEDGEAIEKNLAAMEKAIRQQTSAEPFVDYGPVDFVPAIQKQAFMKMVETAKQHIENGDIFQVVLSQRMKGTLSHDPFYFYRKLRKTNPSPYMFYLDFGGYVILGASPESLIKTKERVVYTNPIAGTRPRAKVPEEDERLENELLHDEKELAEHKMLVDLSRNDLGRVCEPGSIRVQKYMEVERFQHVMHIVSEVRGKLRDGFSGIDALISCLPAGTVSGAPKIRAMQIINSLETLKRGMYAGAVGYINLNGDIDFALAIRSLLIKDNTAYLQSGAGIVYDSDPEKEYEETLNKARSILEVQTHDFIAR
>NZ_CP033687.1|WP_017551428.1|321864_323046_-|FtsX-like-permease-family-protein
MRAAELFFTAIRSLLANRRRSILTMLGIVIGIASVITIISLGKGVEKATLKNLQASNSGKQSTVVEYYADDLNAAESGFNESDLSLLNSAGASFGLAEAHIINDDNGTVDVQASLNGSEQNVTVKLLKRSSSEQEISAGHNISQNNITFADPVALISKKLAASIYIQPNRALDTAVIVNGISYHVIGVFENADDFHDIMIPKKVYKKSNISNVGNKLKLVFNRGENVSKQTKKIVSLLNKQGSHHLQGSYEHIEMGQILKGIGSVINSLTYFISAIAGISLFIAGIGVMNMMYISVSERTREIGIRLAIGATPKNILFQFLLEAVLLTGIGGLIGFGIGGGLAWLISLFLPFRAVIGVGSFLLAFCVSTFVGILFGILPAKNAANKNLIDILR
>NZ_CP033687.1|WP_014097348.1|323042_323726_-|ABC-transporter-ATP-binding-protein
MIRLERLNKYYQQGDEKIHVLKDISLEINQGEFVAIMGPSGSGKSTLINIIGFLDNQFEGEYLFKRNSVIGKSSKDYAKLRNQNVGFVFQNFKLIANLTVAENVGLPLLYAGYRRKDIGERVNNVLQSVHLKGIAKKLPSQLSGGQQQRVAIARALISKPSFLLADEPTGALDRHTSQEILKLFLDLNQKLRSTIIMVTHDYQVASQSQRMIQIMDGRIESDRSVSK

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Crispr_ID: NZ_CP033687_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_3

458563-466896

TypeI

I-C

Consensus_repeat	Method
NATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CRT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	PILER-CR
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CRISPRCasFinder
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	PILER-CR

126 spacers

cas2,cas1,cas4,cas7,cas8c,cas5,cas3

The CRISPR arrays of NZ_CP033687_3

>merge|NZ_CP033687|3|458563-466896|CRT,PILER-CR,CRISPRCasFinder,PILER-CR
GTTTGCTCAGCAAGTATTCATTAGGGAGCGACTTGATGATCCTAGGGATCGCAAATACAGCAAACGATTTCAATCCACGCCCCCATGTAGGGAGCGACCTTGACTGCTTATACAAGATCATTCTATCTCCGCATTTCAATCCACGCCCCCATGTAGGGAGCGACTGGGTTTCTGGTTAACACAAAGGGCCCACGCCTAATTTCAATCCACGCCCCCATGTAGGGAGCGACTTGACCGGGGCTGACGGCGGAGCTGGATTACACGATTTCAATCCACGCCCCCATGTAGGGAGCGACTCATATAGCGTTTTATCACGGAAAATCAATTTCGATTTCAATCCACGCCCCCATGTAGGGAGCGACCCCTTCCAACGGTTTTAACTTTTGCTTTGGGCGTATTTCAATCCACGCCCCCATGTAGGGAGCGACGTTTGATGCTAGAAATATTTCATCTGATTTTGTTATTTCAATCCACGCCCCCATGTAGGGAGCGACCGGCGTCGGGCACATCGAGTTCGTTAGCAGTTCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACATTCGTCTACGATCAGATACACTTTTTTGGCCTATTTCAATCCACGCCCCCATGTAGGGAGCGACTTATGGCATATGCCCGGGAGGAGGTATTGCGATATTTCAATCCACGCCCCCATGTAGGGAGCGACATGGCAGGGATTCCGGCGGTGCTCGGTTATGCCGATTTCAATCCACGCCCCCATGTAGGGAGCGACGGCCAACACTCTCCGCATATGCAGAGTCGCTTATATTTCAATCCACGCCCCCATGTAGGGAGCGACTGATTACCAGTTTAAAAGGGGTATGGGCCTACAAATTTCAATCCACGCCCCCATGTAGGGAGCGACATGGGAGATCTGGTACAGTCGCTTGTCGGACAGGATTTCAATCCACGCCCCCATGTAGGGAGCGACATATGAACATTGAACAATTAAGAAATGCTTGGATTATTTCAATCCACGCCCCCATGTAGGGAGCGACATCGCTCTTTCATTAGGGCGAACAGTGCTTTGTTATTTCAATCCACGCCCCCATGTAGGGAGCGACTGCCGGATATTCCTGGTGCTTTCGGATCCATAATATTTCAATCCACGCCCCCATGTAGGGAGCGACCCCGACGTTCCGGGCTTTTAAATTTAAAGGTTTTGATTTCAATCCACGCCCCCATGTAGGGAGCGACGACAAAATCGTCAGCTACGTTTTCGGGCATAGAATTTCAATCCACGCCCCCATGTAGGGAGCGACGCAAGCTAACTAAGAAAACTAAATATGGCTCCAAATTTCAATCCACGCCCCCATGTAGGGAGCGACAATTAAAGCCGGCGCCTGGACGCGCTTAACAGCGATTTCAATCCACGCCCCCATGTAGGGAGCGACGCGATATGTTTTCAAAAGTAAAATCTTTTAGCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACTGCACAGCAGGAGCGGGACCGGATCGATGCCTGGATTTCAATCCACGCCCCCATGTAGGGAGCGACCAAAACGAACGGTATCCGAGGATGCGCCAATCCAATTTCAATCCACGCCCCCATGTAGGGAGCGACGCTTTGTCCCATCAACGTTGCCAATATATTCCTATTTCAATCCACGCCCCCATGTAGGGAGCGACAATGCTATAAAATTGCAAGCAACATTGGCGTGGGATTTCAATCCACGCCCCCATGTAGGGAGCGACTGGGGATTTATACACCATAGATACACCAGCAACTATTTCAATCCACGCCCCCATGTAGGGAGCGACGATGAATTTACAAAAATTATTTGCTGCACAAGCTATTTCAATCCACGCCCCCATGTAGGGAGCGACTACTAATCTTGTCATTTTTTCGCTCCCCTATTCTATTTCAATCCACGCCCCCATGTAGGGAGCGACGTAAATGTGTCTGTTACTTTTTCATTGTCATCAAATTTCAATCCACGCCCCCATGTAGGGAGCGACAATGATTGTCGGAGATGGTAGCGGAGCGAATCGATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTTTTCGTTGTGCTTCAGTCAATAATTTTTTGTTATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTCACTGGATAGCAGCGGGCGTCCCTATTTTGGCATTTCAATCCACGCCCCCATGTAGGGAGCGACAACGGGGCAGCTGAATGACCGCATTACATTTGTATTTCAATCCACGCCCCCATGTAGGGAGCGACTAAATCAAAGGAGGAACCCTAAAATGATCACAATATTTCAATCCACGCCCCCATGTAGGGAGCGACGCCCGACTCGTCATAGTCGAGGCGGGTTCCCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACAAAATTCTGCGGATAGATTGATAATCGTTTAATATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTGCGGTCATTTTTTTATTGTCCGGTTTGTAAAAATTTCAATCCACGCCCCCATGTAGGGAGCGACATTGCAAAATATAGATATTACTCACTGCAAACGATTTCAATCCACGCCCCCATGTAGGGAGCGACAACAACCATTGGCTGTAACAAATAGCGGCCATCAATTTCAATCCACGCCCCCATGTAGGGAGCGACTACTCGCGGTTGTAATTAGTCGACATCTCGATTTATTTCAATCCACGCCCCCATGTAGGGAGCGACCCCTACAAATTTATTTGTATCTAGGTACAAATTAATTTCAATCCACGCCCCCATGTAGGGAGCGACCTTTCAAGTCCTTTCTTTCGATGTAGCCTTTATATTTCAATCCACGCCCCCATGTAGGGAGCGACTGGTGGAAACGGTTCTTCCGGGCCTTCCACAGGTATTTCAATCCACGCCCCCATGTAGGGAGCGACACAGAAATTTAAAATCCTTGCTGTCGCAGCAGCTATTTCAATCCACGCCCCCATGTAGGGAGCGACCCGGCGCAAACTACCTTTAATGTCGAGGTGACGATTTCAATCCACGCCCCCATGTAGGGAGCGACTCATGATAGAGGCCCATATGAAACGGCGTGTCTATTTCAATCCACGCCCCCATGTAGGGAGCGACGCGGATCGACAAAAATCATATCCGCCAACCGCAATTTCAATCCACGCCCCCATGTAGGGAGCGACGTGGGTTATGGTGGATAAGAGATTATATTGGGAATTTCAATCCACGCCCCCATGTAGGGAGCGACAAGGTCTTGTTAAAGGTATGACAGGCAGCGCAAAATTTCAATCCACGCCCCCATGTAGGGAGCGACCAATGCCATTTTTAAAATAGATGTCAATGGTCGATTTCAATCCACGCCCCCATGTAGGGAGCGACGCGTATTAAGCCTCGTCACCTTTTTAATATGCTATTTCAATCCACGCCCCCATGTAGGGAGCGACAAAGCGTATTAAGCCTCGTCACCTTTTTAATATGCTATTTCAATCCACGCCCCCATGTAGGGAGCGACGTCCTGCGTAAGGGAAAGCCATGTTGCCATTGTTATTTCAATCCACGCCCCCATGTAGGGAGCGACCTTCATGTGCACCAATTGTGTCGTACACTTCCAGATTTCAATCCACGCCCCCATGTAGGGAGCGACGGACGGTCTGCGCGACGGCTGTGTAATTTATGATATTTCAATCCACGCCCCCATGTAGGGAGCGACCCCCGCCGCGTATATGAGGAGGAAACGGAGATTGATTTCAATCCACGCCCCCATGTAGGGAGCGACAACAACCATCGGCTGTAACAAATAGCGGCCATCAATTTCAATCCACGCCCCCATGTAGGGAGCGACGGTTAACTTAAGCGCTGATAATATTGTATCAGATTTCAATCCACGCCCCCATGTAGGGAGCGACCCAGCAAGCAACGGGGCGATATATACACCTTTTGGATTTCAATCCACGCCCCCATGTAGGGAGCGACTCGGTTGCTTTGGTTCCTCTTTCAATTTTAATAATTTCAATCCACGCCCCCATGTAGGGAGCGACCAGCGCTTATGCCAGCCCTACGGAGACGACCAGAATTTCAATCCACGCCCCCATGTAGGGAGCGACTATACCGACAAAGATGTGCTTTCCGCATCGCTTATTTCAATCCACGCCCCCATGTAGGGAGCGACTGCAGACCCGGTAGAATGTGCGCGAGAGGCTATATTTCAATCCACGCCCCCATGTAGGGAGCGACCATTTTGTTTTGTATGCGGAACGACCGAAAACCTAATTTCAATCCACGCCCCCATGTAGGGAGCGACCATTGACCGAATTGGTACATTAAAAAATCCAATAATTTCAATCCACGCCCCCATGTAGGGAGCGACACAGAGGACTCAGCAGTACGTATGGCGGACTTTATTTCAATCCACGCCCCCATGTAGGGAGCGACGTCCAGACCCTAGCACCAGCTCTATGTCGGAATCATTTCAATCCACGCCCCCATGTAGGGAGCGACCCATCCCATGCCTGCTGGCGCAAACTTTATACAGGATTTCAATCCACGCCCCCATGTAGGGAGCGACGTATTAAACCAGGATTCCCATTCTTGTTGATATTATTTCAATCCACGCCCCCATGTAGGGAGCGACCTGAATCCTAACCCATCCGCCATATACTGAAGTATTTCAATCCACGCCCCCATGTAGGGAGCGACGTAGATCAAGTTCTAGCACAACGAGGCATTCAACATTTCAATCCACGCCCCCATGTAGGGAGCGACCTATCAGTGGTGCGAGTGGCGCAAGATGAGATTGATTTCAATCCACGCCCCCATGTAGGGAGCGACGGATATCTGGCGGGAGACACTGCAAAAAGACCTAATTTCAATCCACGCCCCCATGTAGGGAGCGACGGGACTTTTGACGGATTATGACACTACTGTCGATATTTCAATCCACGCCCCCATGTAGGGAGCGACTGAGCACCCTTTATTAATCGTTTATCCCATGAAATTTCAATCCACGCCCCCATGTAGGGAGCGACTCCGCAGGTGACAGATCGATATGAGTACCTTGCGATTTCAATCCACGCCCCCATGTAGGGAGCGACCGGGTGGCTTCGTAAAGCTGCTGTCGTTTCTCCGATTTCAATCCACGCCCCCATGTAGGGAGCGACGCGGTGGCAATAGGTGGCGTAGCATTTACGGCAATTTCAATCCACGCCCCCATGTAGGGAGCGACCTATTACACAAGCACAGAAAGCTATTAGAATAGCATTTCAATCCACGCCCCCATGTAGGGAGCGACTTGATCGGTCATATGAATGTCATTCGTTCCATGTATTTCAATCCACGCCCCCATGTAGGGAGCGACGCCACTATAAGTCAAAAAATACGACATACAATGGATTTCAATCCACGCCCCCATGTAGGGAGCGACGAAATCCTGTAGGCATCAGCACGAAATGTCGCAATTTCAATCCACGCCCCCATGTAGGGAGCGACATGATCATTAAGTCGGCGCCCTGGCCGGTGATAATTTCAATCCACGCCCCCATGTAGGGAGCGACCGCTCTTTCATATGTTGCAAATCCACCGCGTTTATTTCAATCCACGCCCCCATGTAGGGAGCGACGAGAGAGGCATTTATTTTAAAGTACATGGGAGAGATTTCAATCCACGCCCCCATGTAGGGAGCGACCTGTATCAAGTGTCACAACGAGATCCACGGAAAAATTTCAATCCACGCCCCCATGTAGGGAGCGACAATGATAACATTAGTCCTTTGCCTTACAATCGTTATTTCAATCCACGCCCCCATGTAGGGAGCGACAATCAACATCATATCTCATTGCAATTTTCCTAGTATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTGGCTGGGGATGATGTTGTAGAGATTGATGGTATTTCAATCCACGCCCCCATGTAGGGAGCGACTCGGGTAACGATCGACAACCTGCTCATGATATTGATTTCAATCCACGCCCCCATGTAGGGAGCGACCGTTCCAAAGCAGGATCCGGTCGTCGGTTAGCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACCTGGTTCGGAGATTGTATCTGTCCTCAGGATCATATTTCAATCCACGCCCCCATGTAGGGAGCGACCATGCCCCCGGTTCGCATTGTTCCCGTTTCGACATTTCAATCCACGCCCCCATGTAGGGAGCGACGCTTTCTATTTCATTTAGATACGACACGCCACCATTTCAATCCACGCCCCCATGTAGGGAGCGACGTCCAGACCCTAGCACCAGCTCTATGTCGGAATCATTTCAATCCACGCCCCCATGTAGGGAGCGACGCCAGACAATCGCAGAGATGCGGGCAAAAATCAGATTTCAATCCACGCCCCCATGTAGGGAGCGACAATCCTTGCTTGCCTTTTAGACAAAAAAAGGAGGTATTTCAATCCACGCCCCCATGTAGGGAGCGACACGAACAGGCGGACATTTTGCGCCGCAGTCCGCTGATTTCAATCCACGCCCCCATGTAGGGAGCGACGTAATCACGGAGGGCGATACGTTCATTAACGAGATGATTTCAATCCACGCCCCCATGTAGGGAGCGACCTGGCTCGATCAGCTTACAAATCAATTTAGCGCAATTTCAATCCACGCCCCCATGTAGGGAGCGACTTGGCTAGGTGGCGATAACGATAAGGCTGGTCGATTTCAATCCACGCCCCCATGTAGGGAGCGACAGAATACGAACAGCTTGTCATAGAGGCATGGAAATTTCAATCCACGCCCCCATGTAGGGAGCGACAAGTAAATTTGATGATATTGTGACAAATATCATGATTTCAATCCACGCCCCCATGTAGGGAGCGACTTACGGAAAGCACCTAGACGATATGGATTTAACGATTTCAATCCACGCCCCCATGTAGGGAGCGACGATGTAGATTGACGATACCATACGTAACTTTTATATTTCAATCCACGCCCCCATGTAGGGAGCGACGCGCAAAGCGGTTTTATCTTTCATGGCTGCGATGATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTGTTCTCCCATATTCGTTCCTCAGGATGATCAATTTCAATCCACGCCCCCATGTAGGGAGCGACGCAAGCTGAAGGTTGTGGAGAGGGCTGGAATATCATTTCAATCCACGCCCCCATGTAGGGAGCGACACGGCAGGCGGTCGTCGAAGTCGAGCCCTGGACGATTTCAATCCACGCCCCCATGTAGGGAGCGACCTGATTGTTTCGATTGTCGTAATGATTCAGTACAGATTTCAATCCACGCCCCCATGTAGGGAGCGACATTTTCAATGATAATCCTTCTATTTTCAAGTATGATTTCAATCCACGCCCCCATGTAGGGAGCGACGTCTGCGTCCCAGATGCCGTTAATCCCGTACTTTGCATTTCAATCCACGCCCCCATGTAGGGAGCGACCTTCGTAATGGCTTCGTAAGGCGCAAGCGTATATATTTCAATCCACGCCCCCATGTAGGGAGCGACACTTCGACCACGGGCCGGTTAATCCGATCGTAATATTTCAATCCACGCCCCCATGTAGGGAGCGACAGAACAGCACGCCTTTGCTATCGCTTTGCTCAATATTTCAATCCACGCCCCCATGTAGGGAGCGACTCGAGTTCATTCCGCAGCACTTTCGTGATGCCTTCATTTCAATCCACGCCCCCATGTAGGGAGCGACGGCGAGGTCGGCGTGATTGTCGATAACACCGCGATTTCAATCCACGCCCCCATGTAGGGAGCGACGCAGATGGGGATCAGCAAGGCGATAGGATTTATATTTCAATCCACGCCCCCATGTAGGGAGCGACGGTTGCTAGTTGCTCCATATGGGATGGCAAGACCGATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTTTTGCTCAAGCTCATCAATTCTTTTCTCAAGAATTTCAATCCACGCCCCCATGTAGGGAGCGACAGTAATGCTTCCAATCGCCAGGTCGTGTCGGTCATTTCAATCCACGCCCCCATGTAGGGAGCGACGTTAAAAGCATATCTGAAATTCTTAAAATACACTATTTCAATCCACGCCCCCATGTAGGGAGCGACGGTTTGCGCTCAAAGGCGAATTTTTGAGGTCACAATTTCAATCCACGCCCCCATGTAGGGAGCGACTATCGCGTGCAAGCCCATTGAGATTGAGGATTTGATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTCTTCCTTAAGATTTGTAAGCAGTCCGATTAAATTTCAATCCACGCCCCCATGTAGTATGTGTC

>NZ_CP033687|3|1|458563-466896|CRT
GTTTGCTCAGCAAGTATTCATTAGGGAGCGAC	TTGATGATCCTAGGGATCGCAAATACAGCAAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTGACTGCTTATACAAGATCATTCTATCTCCGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGTTTCTGGTTAACACAAAGGGCCCACGCCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGACCGGGGCTGACGGCGGAGCTGGATTACACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATATAGCGTTTTATCACGGAAAATCAATTTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTTCCAACGGTTTTAACTTTTGCTTTGGGCGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTTGATGCTAGAAATATTTCATCTGATTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGCGTCGGGCACATCGAGTTCGTTAGCAGTTCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTCGTCTACGATCAGATACACTTTTTTGGCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTATGGCATATGCCCGGGAGGAGGTATTGCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGCAGGGATTCCGGCGGTGCTCGGTTATGCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCAACACTCTCCGCATATGCAGAGTCGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGATTACCAGTTTAAAAGGGGTATGGGCCTACAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGGAGATCTGGTACAGTCGCTTGTCGGACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATATGAACATTGAACAATTAAGAAATGCTTGGATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATCGCTCTTTCATTAGGGCGAACAGTGCTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCCGGATATTCCTGGTGCTTTCGGATCCATAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCGACGTTCCGGGCTTTTAAATTTAAAGGTTTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GACAAAATCGTCAGCTACGTTTTCGGGCATAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTAACTAAGAAAACTAAATATGGCTCCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATTAAAGCCGGCGCCTGGACGCGCTTAACAGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGATATGTTTTCAAAAGTAAAATCTTTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCACAGCAGGAGCGGGACCGGATCGATGCCTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAAAACGAACGGTATCCGAGGATGCGCCAATCCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTGTCCCATCAACGTTGCCAATATATTCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGCTATAAAATTGCAAGCAACATTGGCGTGGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGGATTTATACACCATAGATACACCAGCAACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGAATTTACAAAAATTATTTGCTGCACAAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTAATCTTGTCATTTTTTCGCTCCCCTATTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAAATGTGTCTGTTACTTTTTCATTGTCATCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATTGTCGGAGATGGTAGCGGAGCGAATCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTCGTTGTGCTTCAGTCAATAATTTTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCACTGGATAGCAGCGGGCGTCCCTATTTTGGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACGGGGCAGCTGAATGACCGCATTACATTTGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAAATCAAAGGAGGAACCCTAAAATGATCACAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCCGACTCGTCATAGTCGAGGCGGGTTCCCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAATTCTGCGGATAGATTGATAATCGTTTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGCGGTCATTTTTTTATTGTCCGGTTTGTAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTGCAAAATATAGATATTACTCACTGCAAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATTGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTCGCGGTTGTAATTAGTCGACATCTCGATTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTACAAATTTATTTGTATCTAGGTACAAATTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTTCAAGTCCTTTCTTTCGATGTAGCCTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGTGGAAACGGTTCTTCCGGGCCTTCCACAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAAATTTAAAATCCTTGCTGTCGCAGCAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGGCGCAAACTACCTTTAATGTCGAGGTGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATGATAGAGGCCCATATGAAACGGCGTGTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGATCGACAAAAATCATATCCGCCAACCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTGGGTTATGGTGGATAAGAGATTATATTGGGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGGTCTTGTTAAAGGTATGACAGGCAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAATGCCATTTTTAAAATAGATGTCAATGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAGCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCTGCGTAAGGGAAAGCCATGTTGCCATTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCATGTGCACCAATTGTGTCGTACACTTCCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGACGGTCTGCGCGACGGCTGTGTAATTTATGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCCGCCGCGTATATGAGGAGGAAACGGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATCGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTAACTTAAGCGCTGATAATATTGTATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCAGCAAGCAACGGGGCGATATATACACCTTTTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGTTGCTTTGGTTCCTCTTTCAATTTTAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAGCGCTTATGCCAGCCCTACGGAGACGACCAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATACCGACAAAGATGTGCTTTCCGCATCGCTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCAGACCCGGTAGAATGTGCGCGAGAGGCTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTTTGTTTTGTATGCGGAACGACCGAAAACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGACCGAATTGGTACATTAAAAAATCCAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAGGACTCAGCAGTACGTATGGCGGACTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATCCCATGCCTGCTGGCGCAAACTTTATACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTATTAAACCAGGATTCCCATTCTTGTTGATATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGAATCCTAACCCATCCGCCATATACTGAAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAGATCAAGTTCTAGCACAACGAGGCATTCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATCAGTGGTGCGAGTGGCGCAAGATGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGATATCTGGCGGGAGACACTGCAAAAAGACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGGACTTTTGACGGATTATGACACTACTGTCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGAGCACCCTTTATTAATCGTTTATCCCATGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCGCAGGTGACAGATCGATATGAGTACCTTGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGGTGGCTTCGTAAAGCTGCTGTCGTTTCTCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGTGGCAATAGGTGGCGTAGCATTTACGGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATTACACAAGCACAGAAAGCTATTAGAATAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGATCGGTCATATGAATGTCATTCGTTCCATGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCACTATAAGTCAAAAAATACGACATACAATGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAAATCCTGTAGGCATCAGCACGAAATGTCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGATCATTAAGTCGGCGCCCTGGCCGGTGATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGCTCTTTCATATGTTGCAAATCCACCGCGTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAGAGAGGCATTTATTTTAAAGTACATGGGAGAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGTATCAAGTGTCACAACGAGATCCACGGAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATAACATTAGTCCTTTGCCTTACAATCGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCAACATCATATCTCATTGCAATTTTCCTAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGGCTGGGGATGATGTTGTAGAGATTGATGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGGTAACGATCGACAACCTGCTCATGATATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGTTCCAAAGCAGGATCCGGTCGTCGGTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGTTCGGAGATTGTATCTGTCCTCAGGATCAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATGCCCCCGGTTCGCATTGTTCCCGTTTCGAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTCTATTTCATTTAGATACGACACGCCACC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCAGACAATCGCAGAGATGCGGGCAAAAATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCCTTGCTTGCCTTTTAGACAAAAAAAGGAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGAACAGGCGGACATTTTGCGCCGCAGTCCGCTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAATCACGGAGGGCGATACGTTCATTAACGAGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGCTCGATCAGCTTACAAATCAATTTAGCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGGCTAGGTGGCGATAACGATAAGGCTGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATACGAACAGCTTGTCATAGAGGCATGGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGTAAATTTGATGATATTGTGACAAATATCATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTACGGAAAGCACCTAGACGATATGGATTTAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTAGATTGACGATACCATACGTAACTTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGCAAAGCGGTTTTATCTTTCATGGCTGCGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGTTCTCCCATATTCGTTCCTCAGGATGATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTGAAGGTTGTGGAGAGGGCTGGAATATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGGCAGGCGGTCGTCGAAGTCGAGCCCTGGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGATTGTTTCGATTGTCGTAATGATTCAGTACAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTTTCAATGATAATCCTTCTATTTTCAAGTATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCTGCGTCCCAGATGCCGTTAATCCCGTACTTTGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCGTAATGGCTTCGTAAGGCGCAAGCGTATAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTTCGACCACGGGCCGGTTAATCCGATCGTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAACAGCACGCCTTTGCTATCGCTTTGCTCAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGAGTTCATTCCGCAGCACTTTCGTGATGCCTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCGAGGTCGGCGTGATTGTCGATAACACCGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAGATGGGGATCAGCAAGGCGATAGGATTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTGCTAGTTGCTCCATATGGGATGGCAAGACCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTGCTCAAGCTCATCAATTCTTTTCTCAAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGTAATGCTTCCAATCGCCAGGTCGTGTCGGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTAAAAGCATATCTGAAATTCTTAAAATACACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTTGCGCTCAAAGGCGAATTTTTGAGGTCACA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATCGCGTGCAAGCCCATTGAGATTGAGGATTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCTTCCTTAAGATTTGTAAGCAGTCCGATTAA
ATTTCAATCCACGCCCCCATGTAGTATGTGTC

>NZ_CP033687|3|1|458629-459517|PILER-CR
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTGACTGCTTATACAAGATCATTCTATCTCCGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGTTTCTGGTTAACACAAAGGGCCCACGCCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGACCGGGGCTGACGGCGGAGCTGGATTACACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATATAGCGTTTTATCACGGAAAATCAATTTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTTCCAACGGTTTTAACTTTTGCTTTGGGCGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTTGATGCTAGAAATATTTCATCTGATTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGCGTCGGGCACATCGAGTTCGTTAGCAGTTCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTCGTCTACGATCAGATACACTTTTTTGGCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTATGGCATATGCCCGGGAGGAGGTATTGCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGCAGGGATTCCGGCGGTGCTCGGTTATGCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCAACACTCTCCGCATATGCAGAGTCGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGATTACCAGTTTAAAAGGGGTATGGGCCTACAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGGAGATCTGGTACAGTCGCTTGTCGGACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGACATATGAACATTGAACAATTAAGAAATGCTTGGATTATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATCGCTCTTTCATTAGGGCGAACAGTGCTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCCGGATATTCCTGGTGCTTTCGGATCCATAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCGACGTTCCGGGCTTTTAAATTTAAAGGTTTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GACAAAATCGTCAGCTACGTTTTCGGGCATAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTAACTAAGAAAACTAAATATGGCTCCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATTAAAGCCGGCGCCTGGACGCGCTTAACAGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGATATGTTTTCAAAAGTAAAATCTTTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCACAGCAGGAGCGGGACCGGATCGATGCCTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAAAACGAACGGTATCCGAGGATGCGCCAATCCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTGTCCCATCAACGTTGCCAATATATTCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGCTATAAAATTGCAAGCAACATTGGCGTGGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGGATTTATACACCATAGATACACCAGCAACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGAATTTACAAAAATTATTTGCTGCACAAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTAATCTTGTCATTTTTTCGCTCCCCTATTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAAATGTGTCTGTTACTTTTTCATTGTCATCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATTGTCGGAGATGGTAGCGGAGCGAATCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTCGTTGTGCTTCAGTCAATAATTTTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCACTGGATAGCAGCGGGCGTCCCTATTTTGGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACGGGGCAGCTGAATGACCGCATTACATTTGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAAATCAAAGGAGGAACCCTAAAATGATCACAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCCGACTCGTCATAGTCGAGGCGGGTTCCCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAATTCTGCGGATAGATTGATAATCGTTTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGCGGTCATTTTTTTATTGTCCGGTTTGTAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTGCAAAATATAGATATTACTCACTGCAAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATTGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTCGCGGTTGTAATTAGTCGACATCTCGATTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTACAAATTTATTTGTATCTAGGTACAAATTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTTCAAGTCCTTTCTTTCGATGTAGCCTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGTGGAAACGGTTCTTCCGGGCCTTCCACAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAAATTTAAAATCCTTGCTGTCGCAGCAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGGCGCAAACTACCTTTAATGTCGAGGTGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATGATAGAGGCCCATATGAAACGGCGTGTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGATCGACAAAAATCATATCCGCCAACCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTGGGTTATGGTGGATAAGAGATTATATTGGGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGGTCTTGTTAAAGGTATGACAGGCAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAATGCCATTTTTAAAATAGATGTCAATGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAGCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCTGCGTAAGGGAAAGCCATGTTGCCATTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCATGTGCACCAATTGTGTCGTACACTTCCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGACGGTCTGCGCGACGGCTGTGTAATTTATGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCCGCCGCGTATATGAGGAGGAAACGGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATCGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTAACTTAAGCGCTGATAATATTGTATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCAGCAAGCAACGGGGCGATATATACACCTTTTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGTTGCTTTGGTTCCTCTTTCAATTTTAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAGCGCTTATGCCAGCCCTACGGAGACGACCAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATACCGACAAAGATGTGCTTTCCGCATCGCTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCAGACCCGGTAGAATGTGCGCGAGAGGCTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTTTGTTTTGTATGCGGAACGACCGAAAACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGACCGAATTGGTACATTAAAAAATCCAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAGGACTCAGCAGTACGTATGGCGGACTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATCCCATGCCTGCTGGCGCAAACTTTATACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTATTAAACCAGGATTCCCATTCTTGTTGATATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGAATCCTAACCCATCCGCCATATACTGAAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAGATCAAGTTCTAGCACAACGAGGCATTCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATCAGTGGTGCGAGTGGCGCAAGATGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGATATCTGGCGGGAGACACTGCAAAAAGACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGGACTTTTGACGGATTATGACACTACTGTCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGAGCACCCTTTATTAATCGTTTATCCCATGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCGCAGGTGACAGATCGATATGAGTACCTTGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGGTGGCTTCGTAAAGCTGCTGTCGTTTCTCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGTGGCAATAGGTGGCGTAGCATTTACGGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATTACACAAGCACAGAAAGCTATTAGAATAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGATCGGTCATATGAATGTCATTCGTTCCATGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCACTATAAGTCAAAAAATACGACATACAATGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAAATCCTGTAGGCATCAGCACGAAATGTCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGATCATTAAGTCGGCGCCCTGGCCGGTGATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGCTCTTTCATATGTTGCAAATCCACCGCGTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAGAGAGGCATTTATTTTAAAGTACATGGGAGAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGTATCAAGTGTCACAACGAGATCCACGGAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATAACATTAGTCCTTTGCCTTACAATCGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCAACATCATATCTCATTGCAATTTTCCTAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGGCTGGGGATGATGTTGTAGAGATTGATGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGGTAACGATCGACAACCTGCTCATGATATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGTTCCAAAGCAGGATCCGGTCGTCGGTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGTTCGGAGATTGTATCTGTCCTCAGGATCAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATGCCCCCGGTTCGCATTGTTCCCGTTTCGAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTCTATTTCATTTAGATACGACACGCCACC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCAGACAATCGCAGAGATGCGGGCAAAAATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCCTTGCTTGCCTTTTAGACAAAAAAAGGAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGAACAGGCGGACATTTTGCGCCGCAGTCCGCTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAATCACGGAGGGCGATACGTTCATTAACGAGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGCTCGATCAGCTTACAAATCAATTTAGCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGGCTAGGTGGCGATAACGATAAGGCTGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATACGAACAGCTTGTCATAGAGGCATGGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGTAAATTTGATGATATTGTGACAAATATCATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTACGGAAAGCACCTAGACGATATGGATTTAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTAGATTGACGATACCATACGTAACTTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGCAAAGCGGTTTTATCTTTCATGGCTGCGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGTTCTCCCATATTCGTTCCTCAGGATGATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTGAAGGTTGTGGAGAGGGCTGGAATATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGGCAGGCGGTCGTCGAAGTCGAGCCCTGGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGATTGTTTCGATTGTCGTAATGATTCAGTACAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTTTCAATGATAATCCTTCTATTTTCAAGTATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCTGCGTCCCAGATGCCGTTAATCCCGTACTTTGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCGTAATGGCTTCGTAAGGCGCAAGCGTATAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTTCGACCACGGGCCGGTTAATCCGATCGTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAACAGCACGCCTTTGCTATCGCTTTGCTCAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGAGTTCATTCCGCAGCACTTTCGTGATGCCTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCGAGGTCGGCGTGATTGTCGATAACACCGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAGATGGGGATCAGCAAGGCGATAGGATTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTGCTAGTTGCTCCATATGGGATGGCAAGACCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTGCTCAAGCTCATCAATTCTTTTCTCAAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGTAATGCTTCCAATCGCCAGGTCGTGTCGGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTAAAAGCATATCTGAAATTCTTAAAATACACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTTGCGCTCAAAGGCGAATTTTTGAGGTCACA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATCGCGTGCAAGCCCATTGAGATTGAGGATTTG


>NZ_CP033687|3|3|458629-466896|CRISPRCasFinder
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTGACTGCTTATACAAGATCATTCTATCTCCGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGTTTCTGGTTAACACAAAGGGCCCACGCCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGACCGGGGCTGACGGCGGAGCTGGATTACACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATATAGCGTTTTATCACGGAAAATCAATTTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTTCCAACGGTTTTAACTTTTGCTTTGGGCGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTTGATGCTAGAAATATTTCATCTGATTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGCGTCGGGCACATCGAGTTCGTTAGCAGTTCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTCGTCTACGATCAGATACACTTTTTTGGCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTATGGCATATGCCCGGGAGGAGGTATTGCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGCAGGGATTCCGGCGGTGCTCGGTTATGCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCAACACTCTCCGCATATGCAGAGTCGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGATTACCAGTTTAAAAGGGGTATGGGCCTACAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGGAGATCTGGTACAGTCGCTTGTCGGACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATATGAACATTGAACAATTAAGAAATGCTTGGATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATCGCTCTTTCATTAGGGCGAACAGTGCTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCCGGATATTCCTGGTGCTTTCGGATCCATAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCGACGTTCCGGGCTTTTAAATTTAAAGGTTTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GACAAAATCGTCAGCTACGTTTTCGGGCATAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTAACTAAGAAAACTAAATATGGCTCCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATTAAAGCCGGCGCCTGGACGCGCTTAACAGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGATATGTTTTCAAAAGTAAAATCTTTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCACAGCAGGAGCGGGACCGGATCGATGCCTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAAAACGAACGGTATCCGAGGATGCGCCAATCCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTGTCCCATCAACGTTGCCAATATATTCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGCTATAAAATTGCAAGCAACATTGGCGTGGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGGATTTATACACCATAGATACACCAGCAACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGAATTTACAAAAATTATTTGCTGCACAAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTAATCTTGTCATTTTTTCGCTCCCCTATTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAAATGTGTCTGTTACTTTTTCATTGTCATCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATTGTCGGAGATGGTAGCGGAGCGAATCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTCGTTGTGCTTCAGTCAATAATTTTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCACTGGATAGCAGCGGGCGTCCCTATTTTGGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACGGGGCAGCTGAATGACCGCATTACATTTGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAAATCAAAGGAGGAACCCTAAAATGATCACAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCCGACTCGTCATAGTCGAGGCGGGTTCCCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAATTCTGCGGATAGATTGATAATCGTTTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGCGGTCATTTTTTTATTGTCCGGTTTGTAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTGCAAAATATAGATATTACTCACTGCAAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATTGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTCGCGGTTGTAATTAGTCGACATCTCGATTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTACAAATTTATTTGTATCTAGGTACAAATTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTTCAAGTCCTTTCTTTCGATGTAGCCTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGTGGAAACGGTTCTTCCGGGCCTTCCACAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAAATTTAAAATCCTTGCTGTCGCAGCAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGGCGCAAACTACCTTTAATGTCGAGGTGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATGATAGAGGCCCATATGAAACGGCGTGTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGATCGACAAAAATCATATCCGCCAACCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTGGGTTATGGTGGATAAGAGATTATATTGGGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGGTCTTGTTAAAGGTATGACAGGCAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAATGCCATTTTTAAAATAGATGTCAATGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAGCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCTGCGTAAGGGAAAGCCATGTTGCCATTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCATGTGCACCAATTGTGTCGTACACTTCCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGACGGTCTGCGCGACGGCTGTGTAATTTATGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCCGCCGCGTATATGAGGAGGAAACGGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATCGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTAACTTAAGCGCTGATAATATTGTATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCAGCAAGCAACGGGGCGATATATACACCTTTTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGTTGCTTTGGTTCCTCTTTCAATTTTAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAGCGCTTATGCCAGCCCTACGGAGACGACCAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATACCGACAAAGATGTGCTTTCCGCATCGCTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCAGACCCGGTAGAATGTGCGCGAGAGGCTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTTTGTTTTGTATGCGGAACGACCGAAAACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGACCGAATTGGTACATTAAAAAATCCAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAGGACTCAGCAGTACGTATGGCGGACTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATCCCATGCCTGCTGGCGCAAACTTTATACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTATTAAACCAGGATTCCCATTCTTGTTGATATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGAATCCTAACCCATCCGCCATATACTGAAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAGATCAAGTTCTAGCACAACGAGGCATTCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATCAGTGGTGCGAGTGGCGCAAGATGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGATATCTGGCGGGAGACACTGCAAAAAGACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGGACTTTTGACGGATTATGACACTACTGTCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGAGCACCCTTTATTAATCGTTTATCCCATGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCGCAGGTGACAGATCGATATGAGTACCTTGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGGTGGCTTCGTAAAGCTGCTGTCGTTTCTCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGTGGCAATAGGTGGCGTAGCATTTACGGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATTACACAAGCACAGAAAGCTATTAGAATAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGATCGGTCATATGAATGTCATTCGTTCCATGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCACTATAAGTCAAAAAATACGACATACAATGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAAATCCTGTAGGCATCAGCACGAAATGTCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGATCATTAAGTCGGCGCCCTGGCCGGTGATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGCTCTTTCATATGTTGCAAATCCACCGCGTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAGAGAGGCATTTATTTTAAAGTACATGGGAGAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGTATCAAGTGTCACAACGAGATCCACGGAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATAACATTAGTCCTTTGCCTTACAATCGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCAACATCATATCTCATTGCAATTTTCCTAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGGCTGGGGATGATGTTGTAGAGATTGATGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGGTAACGATCGACAACCTGCTCATGATATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGTTCCAAAGCAGGATCCGGTCGTCGGTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGTTCGGAGATTGTATCTGTCCTCAGGATCAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATGCCCCCGGTTCGCATTGTTCCCGTTTCGAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTCTATTTCATTTAGATACGACACGCCACC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCAGACAATCGCAGAGATGCGGGCAAAAATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCCTTGCTTGCCTTTTAGACAAAAAAAGGAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGAACAGGCGGACATTTTGCGCCGCAGTCCGCTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAATCACGGAGGGCGATACGTTCATTAACGAGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGCTCGATCAGCTTACAAATCAATTTAGCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGGCTAGGTGGCGATAACGATAAGGCTGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATACGAACAGCTTGTCATAGAGGCATGGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGTAAATTTGATGATATTGTGACAAATATCATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTACGGAAAGCACCTAGACGATATGGATTTAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTAGATTGACGATACCATACGTAACTTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGCAAAGCGGTTTTATCTTTCATGGCTGCGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGTTCTCCCATATTCGTTCCTCAGGATGATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTGAAGGTTGTGGAGAGGGCTGGAATATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGGCAGGCGGTCGTCGAAGTCGAGCCCTGGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGATTGTTTCGATTGTCGTAATGATTCAGTACAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTTTCAATGATAATCCTTCTATTTTCAAGTATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCTGCGTCCCAGATGCCGTTAATCCCGTACTTTGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCGTAATGGCTTCGTAAGGCGCAAGCGTATAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTTCGACCACGGGCCGGTTAATCCGATCGTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAACAGCACGCCTTTGCTATCGCTTTGCTCAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGAGTTCATTCCGCAGCACTTTCGTGATGCCTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCGAGGTCGGCGTGATTGTCGATAACACCGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAGATGGGGATCAGCAAGGCGATAGGATTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTGCTAGTTGCTCCATATGGGATGGCAAGACCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTGCTCAAGCTCATCAATTCTTTTCTCAAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGTAATGCTTCCAATCGCCAGGTCGTGTCGGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTAAAAGCATATCTGAAATTCTTAAAATACACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTTGCGCTCAAAGGCGAATTTTTGAGGTCACA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATCGCGTGCAAGCCCATTGAGATTGAGGATTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCTTCCTTAAGATTTGTAAGCAGTCCGATTAA
ATTTCAATCCACGCCCCCATGTAGTATGTGTC

>NZ_CP033687|3|2|459553-466830|PILER-CR
	CTTGACTGCTTATACAAGATCATTCTATCTCCGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGTTTCTGGTTAACACAAAGGGCCCACGCCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGACCGGGGCTGACGGCGGAGCTGGATTACACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATATAGCGTTTTATCACGGAAAATCAATTTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTTCCAACGGTTTTAACTTTTGCTTTGGGCGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTTGATGCTAGAAATATTTCATCTGATTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGCGTCGGGCACATCGAGTTCGTTAGCAGTTCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTCGTCTACGATCAGATACACTTTTTTGGCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTATGGCATATGCCCGGGAGGAGGTATTGCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGCAGGGATTCCGGCGGTGCTCGGTTATGCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCAACACTCTCCGCATATGCAGAGTCGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGATTACCAGTTTAAAAGGGGTATGGGCCTACAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGGGAGATCTGGTACAGTCGCTTGTCGGACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGACATATGAACATTGAACAATTAAGAAATGCTTGGATTATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATCGCTCTTTCATTAGGGCGAACAGTGCTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCCGGATATTCCTGGTGCTTTCGGATCCATAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCGACGTTCCGGGCTTTTAAATTTAAAGGTTTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GACAAAATCGTCAGCTACGTTTTCGGGCATAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTAACTAAGAAAACTAAATATGGCTCCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATTAAAGCCGGCGCCTGGACGCGCTTAACAGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGATATGTTTTCAAAAGTAAAATCTTTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCACAGCAGGAGCGGGACCGGATCGATGCCTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAAAACGAACGGTATCCGAGGATGCGCCAATCCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTGTCCCATCAACGTTGCCAATATATTCCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGCTATAAAATTGCAAGCAACATTGGCGTGGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGGGATTTATACACCATAGATACACCAGCAACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGAATTTACAAAAATTATTTGCTGCACAAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTAATCTTGTCATTTTTTCGCTCCCCTATTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAAATGTGTCTGTTACTTTTTCATTGTCATCAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATTGTCGGAGATGGTAGCGGAGCGAATCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTCGTTGTGCTTCAGTCAATAATTTTTTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTCACTGGATAGCAGCGGGCGTCCCTATTTTGGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACGGGGCAGCTGAATGACCGCATTACATTTGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAAATCAAAGGAGGAACCCTAAAATGATCACAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCCGACTCGTCATAGTCGAGGCGGGTTCCCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAATTCTGCGGATAGATTGATAATCGTTTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGCGGTCATTTTTTTATTGTCCGGTTTGTAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTGCAAAATATAGATATTACTCACTGCAAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATTGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TACTCGCGGTTGTAATTAGTCGACATCTCGATTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCTACAAATTTATTTGTATCTAGGTACAAATTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTTCAAGTCCTTTCTTTCGATGTAGCCTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGGTGGAAACGGTTCTTCCGGGCCTTCCACAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAAATTTAAAATCCTTGCTGTCGCAGCAGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGGCGCAAACTACCTTTAATGTCGAGGTGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCATGATAGAGGCCCATATGAAACGGCGTGTCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGATCGACAAAAATCATATCCGCCAACCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTGGGTTATGGTGGATAAGAGATTATATTGGGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGGTCTTGTTAAAGGTATGACAGGCAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAATGCCATTTTTAAAATAGATGTCAATGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAAGCGTATTAAGCCTCGTCACCTTTTTAATATGCT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCTGCGTAAGGGAAAGCCATGTTGCCATTGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCATGTGCACCAATTGTGTCGTACACTTCCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGACGGTCTGCGCGACGGCTGTGTAATTTATGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCCCGCCGCGTATATGAGGAGGAAACGGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AACAACCATCGGCTGTAACAAATAGCGGCCATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTAACTTAAGCGCTGATAATATTGTATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCAGCAAGCAACGGGGCGATATATACACCTTTTGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGTTGCTTTGGTTCCTCTTTCAATTTTAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CAGCGCTTATGCCAGCCCTACGGAGACGACCAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATACCGACAAAGATGTGCTTTCCGCATCGCTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGCAGACCCGGTAGAATGTGCGCGAGAGGCTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTTTGTTTTGTATGCGGAACGACCGAAAACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGACCGAATTGGTACATTAAAAAATCCAATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACAGAGGACTCAGCAGTACGTATGGCGGACTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATCCCATGCCTGCTGGCGCAAACTTTATACAGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTATTAAACCAGGATTCCCATTCTTGTTGATATT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGAATCCTAACCCATCCGCCATATACTGAAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAGATCAAGTTCTAGCACAACGAGGCATTCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATCAGTGGTGCGAGTGGCGCAAGATGAGATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGATATCTGGCGGGAGACACTGCAAAAAGACCTA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGGACTTTTGACGGATTATGACACTACTGTCGAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TGAGCACCCTTTATTAATCGTTTATCCCATGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCGCAGGTGACAGATCGATATGAGTACCTTGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGGGTGGCTTCGTAAAGCTGCTGTCGTTTCTCCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGGTGGCAATAGGTGGCGTAGCATTTACGGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTATTACACAAGCACAGAAAGCTATTAGAATAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGATCGGTCATATGAATGTCATTCGTTCCATGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCACTATAAGTCAAAAAATACGACATACAATGG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAAATCCTGTAGGCATCAGCACGAAATGTCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATGATCATTAAGTCGGCGCCCTGGCCGGTGATA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGCTCTTTCATATGTTGCAAATCCACCGCGTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GAGAGAGGCATTTATTTTAAAGTACATGGGAGAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGTATCAAGTGTCACAACGAGATCCACGGAAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATGATAACATTAGTCCTTTGCCTTACAATCGTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCAACATCATATCTCATTGCAATTTTCCTAGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGGCTGGGGATGATGTTGTAGAGATTGATGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGGGTAACGATCGACAACCTGCTCATGATATTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGTTCCAAAGCAGGATCCGGTCGTCGGTTAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGTTCGGAGATTGTATCTGTCCTCAGGATCAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATGCCCCCGGTTCGCATTGTTCCCGTTTCGAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCTTTCTATTTCATTTAGATACGACACGCCACC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCCAGACCCTAGCACCAGCTCTATGTCGGAATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCCAGACAATCGCAGAGATGCGGGCAAAAATCAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AATCCTTGCTTGCCTTTTAGACAAAAAAAGGAGGT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGAACAGGCGGACATTTTGCGCCGCAGTCCGCTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTAATCACGGAGGGCGATACGTTCATTAACGAGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGGCTCGATCAGCTTACAAATCAATTTAGCGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTGGCTAGGTGGCGATAACGATAAGGCTGGTCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATACGAACAGCTTGTCATAGAGGCATGGAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AAGTAAATTTGATGATATTGTGACAAATATCATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTACGGAAAGCACCTAGACGATATGGATTTAACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTAGATTGACGATACCATACGTAACTTTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCGCAAAGCGGTTTTATCTTTCATGGCTGCGATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTGTTCTCCCATATTCGTTCCTCAGGATGATCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAAGCTGAAGGTTGTGGAGAGGGCTGGAATATC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACGGCAGGCGGTCGTCGAAGTCGAGCCCTGGACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTGATTGTTTCGATTGTCGTAATGATTCAGTACAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ATTTTCAATGATAATCCTTCTATTTTCAAGTATG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTCTGCGTCCCAGATGCCGTTAATCCCGTACTTTGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CTTCGTAATGGCTTCGTAAGGCGCAAGCGTATAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTTCGACCACGGGCCGGTTAATCCGATCGTAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAACAGCACGCCTTTGCTATCGCTTTGCTCAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCGAGTTCATTCCGCAGCACTTTCGTGATGCCTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCGAGGTCGGCGTGATTGTCGATAACACCGCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GCAGATGGGGATCAGCAAGGCGATAGGATTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTGCTAGTTGCTCCATATGGGATGGCAAGACCG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTTTGCTCAAGCTCATCAATTCTTTTCTCAAGA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGTAATGCTTCCAATCGCCAGGTCGTGTCGGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GTTAAAAGCATATCTGAAATTCTTAAAATACACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGTTTGCGCTCAAAGGCGAATTTTTGAGGTCACA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TATCGCGTGCAAGCCCATTGAGATTGAGGATTTG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_026684592.1\|471796_472657_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl\|CDD\|187820
NZ_CP033687.1\|WP_035183676.1\|457945_458365_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP033687.1\|WP_026684954.1\|453059_454205_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|236506
NZ_CP033687.1\|WP_110134131.1\|467184_468600_-\|ISLre2-like-element-ISBco6-family-transposase	unknown	unknown	gnl\|CDD\|284250
NZ_CP033687.1\|WP_110134173.1\|478351_481591_-\|DEAD/DEAH-box-helicase-family-protein	unknown	unknown	gnl\|CDD\|377999
NZ_CP033687.1\|WP_061565731.1\|470122_471154_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP033687.1\|WP_046720946.1\|456550_457174_+\|histidine-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|366010
NZ_CP033687.1\|WP_061577465.1\|472680_474561_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl\|CDD\|187887
NZ_CP033687.1\|WP_017551460.1\|450416_450839_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_026684593.1\|471150_471807_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|273040
NZ_CP033687.1\|WP_142010191.1\|478039_478234_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014097218.1\|445721_446411_-\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|119407
NZ_CP033687.1\|WP_014097216.1\|449783_450392_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_110134172.1\|475478_477905_-\|CRISPR-associated-helicase-Cas3'	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
NZ_CP033687.1\|WP_017551458.1\|451758_452673_-\|DUF1002-domain-containing-protein	unknown	unknown	gnl\|CDD\|377628
NZ_CP033687.1\|WP_026684595.1\|469821_470112_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP033687.1\|WP_035183662.1\|474561_475281_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|273847
NZ_CP033687.1\|WP_110134171.1\|454583_455891_-\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|183075
NZ_CP033687.1\|WP_046720947.1\|450854_451736_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227596
NZ_CP033687.1\|WP_110134170.1\|447961_449497_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225107

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_026684592.1\|471796_472657_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl\|CDD\|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. 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; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	2.89273e-134
NZ_CP033687.1\|WP_026684595.1\|469821_470112_-\|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.	1.60661e-36
NZ_CP033687.1\|WP_026684954.1\|453059_454205_-\|metallophosphoesterase	gnl\|CDD\|236506	PRK09420, cpdB, bifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase.	4.23414e-155
NZ_CP033687.1\|WP_110134131.1\|467184_468600_-\|ISLre2-like-element-ISBco6-family-transposase	gnl\|CDD\|284250	pfam06782, UPF0236, Uncharacterized protein family (UPF0236).	7.48116e-48
NZ_CP033687.1\|WP_110134173.1\|478351_481591_-\|DEAD/DEAH-box-helicase-family-protein	gnl\|CDD\|377999	pfam08455, SNF2_assoc, Bacterial SNF2 helicase associated. This domain is found in bacterial proteins of the SWF/SNF/SWI helicase family to the N-terminus of the SNF2 family N-terminal domain (pfam00176) and together with the Helicase conserved C-terminal domain (pfam00271). The function of the domain is not clear.	3.22154e-102
NZ_CP033687.1\|WP_061565731.1\|470122_471154_-\|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_CP033687.1\|WP_046720946.1\|456550_457174_+\|histidine-phosphatase-family-protein	gnl\|CDD\|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.01398e-69
NZ_CP033687.1\|WP_061577465.1\|472680_474561_-\|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.	5.54126e-178
NZ_CP033687.1\|WP_035183676.1\|457945_458365_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	1.4066e-15
NZ_CP033687.1\|WP_110134172.1\|475478_477905_-\|CRISPR-associated-helicase-Cas3'	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	6.20739e-82
NZ_CP033687.1\|WP_026684593.1\|471150_471807_-\|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.	4.39067e-31
NZ_CP033687.1\|WP_014097218.1\|445721_446411_-\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	5.54843e-67
NZ_CP033687.1\|WP_017551458.1\|451758_452673_-\|DUF1002-domain-containing-protein	gnl\|CDD\|377628	pfam06207, DUF1002, Protein of unknown function (DUF1002). This protein family has no known function. Its members are about 300 amino acids in length. It has so far been detected in Firmicute bacteria and some archaebacteria.	4.74261e-82
NZ_CP033687.1\|WP_035183662.1\|474561_475281_-\|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.	6.65501e-99
NZ_CP033687.1\|WP_110134171.1\|454583_455891_-\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|183075	PRK11283, gltP, glutamate/aspartate:proton symporter; Provisional.	0
NZ_CP033687.1\|WP_046720947.1\|450854_451736_+\|hypothetical-protein	gnl\|CDD\|227596	COG5271, MDN1, AAA ATPase containing von Willebrand factor type A (vWA) domain [General function prediction only].	0.00244629
NZ_CP033687.1\|WP_110134170.1\|447961_449497_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.01506e-19

>NZ_CP033687.1|WP_035183676.1|457945_458365_+|helix-turn-helix-transcriptional-regulator
MADHGNENMENVKEIFAARLKKVRTAQGYSQPELAKKVGVSDRNISNYETGYSFPSIKVLYRISQVLKVSIDYLLGLTNHAGLKTNEAVSNPEKKLLETLSHEPDLYQMMLKDPEKMANRIYQTWNLIRELDDEDDRNT
>NZ_CP033687.1|WP_046720946.1|456550_457174_+|histidine-phosphatase-family-protein
MTLFYFVRHGQTEWNADRNRYCGRSDIGLSQTGVRQAELAAGFLKDIPFNAVYASTLGRAARTAEILVEGRNLKIYQDPRLVETDFGAWEGERQEDFSVKYADNWEAWLKDPGATHAGYTGETAVQVYQRVRACIDELVEKHPEETVLVVAHSMAIRFFVAGTLEVPFKNYRMIPQDNTGITIYKETPENAGFLAINLNTHLSSIKS
>NZ_CP033687.1|WP_110134171.1|454583_455891_-|cation:dicarboxylase-symporter-family-transporter
MKRVSLAWQIFIGLILGIAIGGIFHGNDTVAHILQPFGDFFLRLIKMIVIPIVVSSLIVGVAGAGDMKQVGKLGLKALIYFEIVTTIAIVVGLLAGNLFHPGTGVDMGSLAKTSISSYVETTKETQHNGIVDTILSIVPTNLFESLSQGNMLPIIFFSVMFGIGVAAIGEKGKPVLRFFQGVSEAMFYVTNLVMKVAPIGVFGLIGVTVTQFGLKSLIPLSKLVFTVYGTIIFFVVVVLGLIAWLFRVNIFNLFKILKDELILAYSTASSEAVLPRLMEKMEKFGCPKSITTLVIPTGYSFNLDGSTLYQSLAALFIAQMYGIHMSIGAQISLVLVLMVTSKGIAGVPGVSFVVLLATLGTVGIPLEGLAFIAGIDRILDMARTACNVVGNTLATIIVSKWEGKYDKEKAEAYLAEISGGGHDTDAKDHKYVTES
>NZ_CP033687.1|WP_026684954.1|453059_454205_-|metallophosphoesterase
MDKKMLLWVAVLSLALFPRTEHADAAFWFQSKRATVDLRLLETSDLHGYMLNYDYAARTEAETYGLALTASLIAAERKTAKNTMLFDDGDLLEGNEMAAYVARRPLKKGEIHPFIRVMNHLNYDAATVGNHDFHYGLDFLKQTINGAKFPFVNANIYYNFEKNDTDDQNFFKPYVILDKKVEDRSGHHHHLKIGVIGFVTPSVIEWEKPSLGGKVKAKDILHTAAWFVPRMKAEGADLIIALAHCGVDPAAKQPFYTGDAVYLLSEVKGIDAILFGHQHRVFPSEFFAGVPGVDIRKGTINGVPAVMPGKWGSHLGVISLTLEKKGEKWEMTQAQSEAKPVYAIHNQQAKSIVRPDPDIVRMTAELQKNVLGSKFTLYSRN
>NZ_CP033687.1|WP_017551458.1|451758_452673_-|DUF1002-domain-containing-protein
MLKRLGWIWFIAMIALGFTMNGVAKASGDNSTVIDEKYGKPIVATGAALSASQKAEVEKELGVDDANNVEEITVTGDDLVHYIPDGNRNSNMYSSAKITRTDSGGIQVNIVTPENITEVTADMYKNALLTAGIKNAEVEVASPLKVTGHSALVGIYKAYDNSDKSGDKLNSDRTEVASQELSVATDLAKKEGLSNDQVTQLLTEIKQEIANQHPATKEDIEKIVDDKLKDLNINLSDSDRQLLYDLFDQMRKLNINFGSVKSELSSLSDKLSDKINKAAGDKDFWQSVKDFFQNIFDAIRGLFQ
>NZ_CP033687.1|WP_046720947.1|450854_451736_+|hypothetical-protein
MVRQVKKTKSFLLTAAFIAFNFCFFTNISVAESPVTDGFIIEADRVEGAMLPPGITAGDTATKQNQVMLRLQYADVTIYGLKITKVLQTPEGPVTIHMNAPGPIQLKNMRVDATKVNFGGIYVPEKARQIGMKNVRLVAHQQLADNADLPGLNLSMETGAADIDTSGSDEETLRKQADQLTQLLQGGTPEKNKEEKNDKSDTADKAKDGTQDKAKTEKQDTEKHNDAKTDGKVTDQNKNKESENTDDTKLDNTGTEPASGQETEKNRTTTKTAQDQSSTDQNVQQKEGSSAEN
>NZ_CP033687.1|WP_017551460.1|450416_450839_+|hypothetical-protein
MGKFHMFRMKFRNWRRSRPFWGATFTLLSGMIILYVPVQLLEIAAAPGSMVSIGLIFGGLIFLIGGMGYFFPKFNMVFGILAIFLSVLSIMGAMGGFFIGTLLGIIGGSLSVSWRVIRQEEVPAGVGPMEEIAAGSAEER
>NZ_CP033687.1|WP_014097216.1|449783_450392_+|hypothetical-protein
MNEGALVLQGQGRTSKKWFFTALLSGLIFLGGLLAVLGINGVAVAATVGGIGKFNVSFKQMQGTGFKLYGSLYGDPSKGEDHVKPVFVNEIDKVTIQDLVISKDVKIPVLGDYQVKITAGDGNTPVHLNGLIQKAALVQGDAVFTNMNISENYVTADDPQAASKAFTQGADTLTIKNGSLDTHYLFQKVANLPNLKVQFVKK
>NZ_CP033687.1|WP_110134170.1|447961_449497_-|helix-turn-helix-transcriptional-regulator
MSLSLNAHMDMVMKHGVDLLRSHQQQIIAECTGILQYLGETHKGSADAFEFAFNCFVAFFRSGQQSVETLIDDIRSQWVKEFHRPPEPHVLIFILTLIENSVHKAIKESTTRSFHLHPSVQYLFSKICEEMLLISKQETFQMDSFCEQLTKSEQLRIEWIARVSHVDGGYRLKKVIGMEENAIDSGLFERTDPSWFWLSEALLKRTPRRKPDERRDVFPVPWKNETLIFCMSDQDVSATIPFLTYAMHLLQMEEERNGKVYAGDQWKDAVILFNEWIMRSQDLNEAIQNIAFGYAQYLPFERCALFRYSQSDAAGFGLFGYHFNNTAIRNIKETIDRFPSISKILLGKGQQVNMVQHFQPLYIPKASEEFPMQYVKEFELESVVVAPIYVPSEGVLIGGAILDQGPGKFFEVDSSTFTALLKFGQSAGELLAKFLKANQWDEKQPELVQLSAREIHILQLLADGASTTEAAEMLHLSEYTVRDYVSSLMKRLHARNRTEAAVKAMRLGLIH
>NZ_CP033687.1|WP_014097218.1|445721_446411_-|LysM-peptidoglycan-binding-domain-containing-protein
MFKLFLDPGHGGKDPGAEGNGLEEKDITLEIAKQIQDILTNHYQNVSVKMSRTTDKFVSLEERTDAANSWGATFFLSIHINSGNGTGFESYIYPESGSATATYQKTIHQEVVKLNDLKDRGRKTADFHVLRESIMPALLTENGFIDTASDAKKMKKNSWIEEVAQGHVNGLAKAFELKKKSGATYHKVVKGDTVYALSKEYGSTIKEIKKWNNLDDDYTIRVGERLRVK
>NZ_CP033687.1|WP_110134131.1|467184_468600_-|ISLre2-like-element-ISBco6-family-transposase
MDIISIIAGLLKDTKSLIEFEEQLKLLMQKAFTQWVGEIFEELDKIIKQEKLEEGWVYCRSDNRNIQFLFGSVTFKRSLMHDKRGNSHYPLDEWLGLVPHQRYSPLVELKVAELASENTYREVADILKEWTAVSLSHTTVGNMVKHVGKTQAEADKALVEELEIAVSLPEGKKVDYLFSEADGVFVRGLKKKQSMEVHHAILYEGWQTNGKRVSLRQPTVIMTTEAIQTFWDEVQATAANTYSLEKTHVITNSDGGAGYTAERFQTAFSQSEFPVLNQLDTYHVAQAIIRTFGGGKSEIKEQIRKAIRTHDLDQFTLYLDTHESTLTDKKALKKIKEFRSYILKNWDRIFDWRDRVKNVPEGARGLGAMESNQRHISFRMKKRGMHWSELGAEAMVKIKQGILNGTLREAYLKHRSRSERKQRNLKQFIRMSQLLKQPVRPSVGVKHGSVALHSSSSSAMGHLSKILELSF
>NZ_CP033687.1|WP_026684595.1|469821_470112_-|CRISPR-associated-endonuclease-Cas2
MLVVITYDVSTLTGAGQKRLRKVAKVCQNYGQRVQNSVFECFVDATQFASLKIELSNIIDPDEDSLRFYQLGNNYKNKVMHIGAKPSLDLEDPLIF
>NZ_CP033687.1|WP_061565731.1|470122_471154_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLLNTLFITQPEVYLSLDGDNIVLLKEKEQLGRLPLHNLESVVAFGYTGVSPALMGYCAERNISLIFFTMNGRFLARVIGKSRGNVVLRKKQYRISDDEIASVQIARNFIIGKIYNQKWILERMTRDYPLRIDVTQFKDVSRFLSAIIKQVRLCDSLETLRGLEGQAAINYNKLFDQMILQQKDDFFFHHRSRRPPLDNVNAMLSFAYTLLANDTASALEGVGLDAYVGFMHQDRPGRVSLALDLMEELRGVYADRFVLSLINTKVINKDDFLKKENGTVIMTDEARKKFLKAWQNKKQEKITHPFLGEKISWGLVPHAQALLLARFLRGDLDEYPPFLWK
>NZ_CP033687.1|WP_026684593.1|471150_471807_-|CRISPR-associated-protein-Cas4
MAFDEDEYLMLSGIQHFQFCKRQWALIHIEQAWEENVRTVEGQNIHQKTDSPFIREKRGSKLIVRAMPIKSNELKLTGICDVVEFVKDKNGVEIYGNEGKYIPYPVEYKRGKPKKNDSDILQLVAQAMCLEEMLLCEVNKGYIFYNEIKRRIEIPITLDEKNKVRKIAAEMQDYYQRRYTPKVKTGPFCNQCSLQNICLPNIIRKRAVSSYIEGKINE
>NZ_CP033687.1|WP_026684592.1|471796_472657_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MSALDHKIDFAVVLSVTKANPNGDPLNGNRPRQNYDGYGEISDVAIKRKIRNRLQDMGESIFVQSNDRKNDSYNSLKERADANPELNKIFKSKDGSGETFAAIACQEWIDVRSFGQVFAFKGSGNKGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDFGVYVLYGSINPQLAEKTGFSNEDAEKIKQALVTLFENDASSARPEGSMEVKKVYWWEHQSKLGQYSSAKVHRSLAVTPLVDNPKTFEDYEITLNELSGLKVDVIDGI
>NZ_CP033687.1|WP_061577465.1|472680_474561_-|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQANEEQVGKIEKKRNDQEYTLLPVSHTTQTAHLEVQVTEDGNFYYAEVINDKKDAVTLIPCTEESSSRAGKKIAPYPLHDKLIYVAGDFVAYGGKIEEPFSYYIQQLGEWANSPFSNAKVQSIYAYLKKKQLIHDLVEAGILFLDNNGQLIDKWDSKYGDKPPLYSTVTGSVESAFVRFTVYSPEKILTKVWKDPEMYESFIKFYNQHLSDRDLCYVTGEFLPSTERHANKIRNSGDKAKLISANDSSGFTYRGRFTESKQVASISYKASQKAHNALKWLINKQGKIIDNRVFLVWENGGNEVPSVTEDSYDITSLDPFANGNNPKIAFTNQEFAREFSKAMDGYKSNLSTEASINILVLDSATTGRMAVLYYRNLNKEIYFENLVKWHTTCAWLHRYRKNEDNQPILFFGAPATKDIAFAAYGPNASDKVVKGLMERMLPCIVEGRRIPTDIVRSALRRASNPVALEKWEWEKILSIACALINKEEGYNLALDKENNNRDYLFGRLLAIADVFERNALDSGENRATNAIRYMNAFSQHPARTWGTIQASLQPYQVRLGKKGTYYAMLIDEVASKLKYEDFNDRPLSGKFLLGFYSQRYDLYQKKETNTVGQTKE
>NZ_CP033687.1|WP_035183662.1|474561_475281_-|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFEVYGKYALFTDPLTKMGGEKLSYQIPTYQALKGIVESIYWKPTILMIIDDLRVMNPIKMESKGVRPIEYNGGNTLANYTYLRDVRYKVRAHFIFNPHRPDLAFDRNEHKHHNILKRSLKAGGRRDIFLGARECQGYVEPCVFEEGEGYYDQTEEVYFGTMVHGINYPDETGRNEMEVRLWNPVMKNGVIHFIRPDECKLVRRVAEMEMKAFTKDNVESADVLLKELERGGEL
>NZ_CP033687.1|WP_110134172.1|475478_477905_-|CRISPR-associated-helicase-Cas3'
MEYIAHIRESDKKVQTVEEHLLAAKELAETYGEKIGVKHITGLAALLHDLGKYTSAFRNYILEAVNNPDHPPKRGSVDHSTAGGKLLFKMFHSGKASPHKALLTEIVGNAIISHHSYLQDFISPEMDLKYLNRVDSKEIDEFETAKENFFEKVMSPTRFSSYVNQAEIELKNFIMKDASKTLTHKMMFLTKYIFSALIDADRTNTRLFEENKPKKEQFPVSKLFNQYYEKLLLTLDSYKENSSANARINRLRSEMSEQCDAFAEKPSGIYTLSIPTGGGKTFASLRYALKHAQLYNKKRIIYIVPFTTIIEQNAEEVRKVLQDDVNILEHHSNVVEDADENDEQQDGIMSVQQRLKLAKDNWDVPIIFTTMVQFLNVFYAKGSRNIRRLHNMSEAVLIFDEVQKVPVPCISLFNEALNFLKTYCHSSILLCTATQPALNYVEHQLQVSPNPEIIRGLDNVIDAFKRVEIVDRATDETFNTEKLANFIEKRMTEVSSVLVILNTKGVVKKLYEHLNSNDNNINIFHLSTSMCAAHRNQILEEVRHCLDAGKKVICVSTQLIEAGVDVSFECVIRSLAGLDSIAQAAGRCNRHGEKETGFVYVINHEEENLSRLPEIKKGKETSKRIFIDLKNTPSIYNGNVLSIQAMEKYFKEFYTAFDANLDYNVPSLQKNMVEMLTTDPNNYSYVRAYCSNTKKKYPLFLSSSFYTAAEKFRVIDDKTTSVIVPFGKGNDVIAELSSNATIEDLSKLMKKAQQYTINLYSQELGKLERNGGIISLFDGKILALKEGAYDHEFGLNVENDSELDFLSI
>NZ_CP033687.1|WP_142010191.1|478039_478234_-|hypothetical-protein
MGLSARIARMLQVSRLREAFADALNKVFAAFSKDASGLPIARLSLPREMAGYIKENYLVGTFPA
>NZ_CP033687.1|WP_110134173.1|478351_481591_-|DEAD/DEAH-box-helicase-family-protein
MVDYLLFEEDVEMMYSPAIFHRGMSYYMQGRVKKLIFNKDSTWTAIVKGSKTYYVTIYYDEEFGEFSNVCTCPAHEQYGECKHEVAAMLAIANGEEEAAEPNIGDVSETHQHMKTLQLMNIFSGLQQSMMETKHNAARKPLRLEYFLKATNVSGFGSDHFLTIEIKIGPGRTYVVRDIKDFLGNVSRGNPHAFTKNFIYDPDEHAFEEEDKEIVEMLLYMLSTQQLYEASMDRWYRFALERELVIPPFIARPLIKKLANRKCKFKYERYAADSIVLHQEEELPLSFRLDGNSQGGPGFLLQLKSLRDLLLFEQYGLAFYKGGFYELSTDQLALLTALEDFYKKSGDEVEIQQEQMSPFLSNVLPGLKRIGKVKLTKDIKGKIVQPKLQTKIFMDNEDEKITLRIEHHYGSRVIDPFMDEETPDDDKILLRDVEKEQKIMTMIEQSPLKYNGKQLYLENDEEALYEFIFTILPQLEEEAEVYIAGAIKSYFQTSHYTPLTSVDMDTSGNFLEVNFDMDGIDEEEIRNVLRSVIEKKRYYRLPDGAFVSLESDEFEHIGQLLGELHVSKKELEDTRLKVPLYRGLQVEELMKTRDKYAVKFGKAFRKLVQQLKNPEDTDFELPKGLEAKMRDYQVTGFQWFKSLAFYRLGGILADDMGLGKTLQSISYMLSEKEANPDIKPFLVVAPASLIYNWKSEIEKFAPGLSSMVIAGTPSERKAFFEAGELPDVLITSYPTLRQDIEEYEKIEFDTLILDEAQAIKNYATKTAAAVRNVQAGRRFALSGTPIENSIDELWSIFQAVLPGFFPPLPEFRKMEQEKISRMVRPFILRRVKKDVLKELPDKIETNHLSELTKPQKELYLAYLDRIRHETAQTLAEGDFNRNRIKILAGLTRLRQLCCHPSLFVENYRGDSGKLEQLVELAHTAIENGKRLLIFSQFSSMLQMIRTRLSDEGIDSFYLDGQTPSRERVEMADRFNSGEKNVFLISLKAGGTGLNLTGADTVVLYDLWWNPAVEEQAAGRAHRIGQKNVVQVIRLIARGTIEEKIYELQQKKKELIEQVIQPGETMLNSLNEEEIKELLGM

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Crispr_ID: NZ_CP033687_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_4

468697-469653

TypeI

I-C

Consensus_repeat	Method
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CRISPRCasFinder
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CRT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	PILER-CR

14 spacers

cas2,cas1,cas4,cas7,cas8c,cas5,cas3

The CRISPR arrays of NZ_CP033687_4

>merge|NZ_CP033687|4|468697-469653|CRISPRCasFinder,CRT,PILER-CR
AATTTTACACATACCCCCATGTAGGGAGCGACTCGTATAATTTTTTGTTTTAAATACACCATTTTTATTTCAATCCACGCCCCCATGTAGGGAGCGACGATGTATTCAGCCCCAATCGGCAAATCCATTTTCATTTCAATCCACGCCCCCATGTAGGGAGCGACGATTACAAAAGCTGAATTCCAGGATAAGCGCAAAATTTCAATCCACGCCCCCATGTAGGGAGCGACGGCCTTTCCTGGCAATCTTGGAAACATGTATACGATTTCAATCCACGCCCCCATGTAGGGAGCGACCCGAGCTAAAGCGGAGCCACCTACTCCGCCAGCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACCGACACCAATTAAATCTGCAACATATCCTTGAGTCATTTCAATCCACGCCCCCATGTAGGGAGCGACACTCCACAACTTTGAGGAGTCAACTTACACCAACATTTCAATCCACGCCCCCATGTAGGGAGCGACCATCAGGCTCATTAATGCATTCTATGATCGGCTCATTTCAATCCACGCCCCCATGTAGGGAGCGACTTTTCCATCTATAAAAAACGTTCCATTTCATAAGATTTCAATCCACGCCCCCATGTAGGGAGCGACCCATATTGCTTGGCCAACTTAGCACGTGCACTATTTCAATCCACGCCCCCATGTAGGGAGCGACAGAATTGCTTCTCGGTTTCGACATATGGTAAAATATTTCAATCCACGCCCCCATGTAGGGAGCGACTCCACGTGCCGGCGTATGGTCCGTCGAGATTGCAATTTCAATCCACGCCCCCATGTAGGGAGCGACTAACCCAATACGGAATCGCTGACTTATACGCTTATATTTCAATCCACGCCCCCATGTAGGGAGCGACCATTGAAGCGCGCGTAATTGCCTGGCTTGCGAGCATTTCAATCCACGCCCCCATGTAGGGAGCGAC

>NZ_CP033687|4|4|468697-469653|CRISPRCasFinder
AATTTTACACATACCCCCATGTAGGGAGCGAC	TCGTATAATTTTTTGTTTTAAATACACCATTTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTATTCAGCCCCAATCGGCAAATCCATTTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATTACAAAAGCTGAATTCCAGGATAAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCTTTCCTGGCAATCTTGGAAACATGTATACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGAGCTAAAGCGGAGCCACCTACTCCGCCAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGACACCAATTAAATCTGCAACATATCCTTGAGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTCCACAACTTTGAGGAGTCAACTTACACCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATCAGGCTCATTAATGCATTCTATGATCGGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTCCATCTATAAAAAACGTTCCATTTCATAAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATATTGCTTGGCCAACTTAGCACGTGCACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATTGCTTCTCGGTTTCGACATATGGTAAAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCACGTGCCGGCGTATGGTCCGTCGAGATTGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAACCCAATACGGAATCGCTGACTTATACGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGAAGCGCGCGTAATTGCCTGGCTTGCGAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC

>NZ_CP033687|4|2|468697-469653|CRT
AATTTTACACATACCCCCATGTAGGGAGCGAC	TCGTATAATTTTTTGTTTTAAATACACCATTTTT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTATTCAGCCCCAATCGGCAAATCCATTTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATTACAAAAGCTGAATTCCAGGATAAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCTTTCCTGGCAATCTTGGAAACATGTATACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGAGCTAAAGCGGAGCCACCTACTCCGCCAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGACACCAATTAAATCTGCAACATATCCTTGAGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTCCACAACTTTGAGGAGTCAACTTACACCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATCAGGCTCATTAATGCATTCTATGATCGGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTCCATCTATAAAAAACGTTCCATTTCATAAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATATTGCTTGGCCAACTTAGCACGTGCACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATTGCTTCTCGGTTTCGACATATGGTAAAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCACGTGCCGGCGTATGGTCCGTCGAGATTGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAACCCAATACGGAATCGCTGACTTATACGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGAAGCGCGCGTAATTGCCTGGCTTGCGAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC

>NZ_CP033687|4|3|468763-469653|PILER-CR
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATGTATTCAGCCCCAATCGGCAAATCCATTTTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GATTACAAAAGCTGAATTCCAGGATAAGCGCAAA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	GGCCTTTCCTGGCAATCTTGGAAACATGTATACG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCGAGCTAAAGCGGAGCCACCTACTCCGCCAGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CGACACCAATTAAATCTGCAACATATCCTTGAGTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	ACTCCACAACTTTGAGGAGTCAACTTACACCAAC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATCAGGCTCATTAATGCATTCTATGATCGGCTC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TTTTCCATCTATAAAAAACGTTCCATTTCATAAG
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CCATATTGCTTGGCCAACTTAGCACGTGCACT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	AGAATTGCTTCTCGGTTTCGACATATGGTAAAAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TCCACGTGCCGGCGTATGGTCCGTCGAGATTGCA
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	TAACCCAATACGGAATCGCTGACTTATACGCTTAT
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC	CATTGAAGCGCGCGTAATTGCCTGGCTTGCGAGC
ATTTCAATCCACGCCCCCATGTAGGGAGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_110134172.1\|475478_477905_-\|CRISPR-associated-helicase-Cas3'	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
NZ_CP033687.1\|WP_110134171.1\|454583_455891_-\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|183075
NZ_CP033687.1\|WP_026684954.1\|453059_454205_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|236506
NZ_CP033687.1\|WP_110134131.1\|467184_468600_-\|ISLre2-like-element-ISBco6-family-transposase	unknown	unknown	gnl\|CDD\|284250
NZ_CP033687.1\|WP_110134173.1\|478351_481591_-\|DEAD/DEAH-box-helicase-family-protein	unknown	unknown	gnl\|CDD\|377999
NZ_CP033687.1\|WP_061565731.1\|470122_471154_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP033687.1\|WP_046720946.1\|456550_457174_+\|histidine-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|366010
NZ_CP033687.1\|WP_061577465.1\|472680_474561_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl\|CDD\|187887
NZ_CP033687.1\|WP_035183676.1\|457945_458365_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP033687.1\|WP_017551460.1\|450416_450839_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_026684593.1\|471150_471807_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|273040
NZ_CP033687.1\|WP_142010191.1\|478039_478234_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_026684592.1\|471796_472657_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl\|CDD\|187820
NZ_CP033687.1\|WP_014097216.1\|449783_450392_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_017551458.1\|451758_452673_-\|DUF1002-domain-containing-protein	unknown	unknown	gnl\|CDD\|377628
NZ_CP033687.1\|WP_017552101.1\|481740_482328_+\|nitroreductase-family-protein	unknown	unknown	gnl\|CDD\|380315
NZ_CP033687.1\|WP_035183662.1\|474561_475281_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|273847
NZ_CP033687.1\|WP_026684595.1\|469821_470112_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP033687.1\|WP_046720947.1\|450854_451736_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227596
NZ_CP033687.1\|WP_110134170.1\|447961_449497_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225107

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_110134172.1\|475478_477905_-\|CRISPR-associated-helicase-Cas3'	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	6.20739e-82
NZ_CP033687.1\|WP_110134171.1\|454583_455891_-\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|183075	PRK11283, gltP, glutamate/aspartate:proton symporter; Provisional.	0
NZ_CP033687.1\|WP_026684954.1\|453059_454205_-\|metallophosphoesterase	gnl\|CDD\|236506	PRK09420, cpdB, bifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase.	4.23414e-155
NZ_CP033687.1\|WP_110134131.1\|467184_468600_-\|ISLre2-like-element-ISBco6-family-transposase	gnl\|CDD\|284250	pfam06782, UPF0236, Uncharacterized protein family (UPF0236).	7.48116e-48
NZ_CP033687.1\|WP_110134173.1\|478351_481591_-\|DEAD/DEAH-box-helicase-family-protein	gnl\|CDD\|377999	pfam08455, SNF2_assoc, Bacterial SNF2 helicase associated. This domain is found in bacterial proteins of the SWF/SNF/SWI helicase family to the N-terminus of the SNF2 family N-terminal domain (pfam00176) and together with the Helicase conserved C-terminal domain (pfam00271). The function of the domain is not clear.	3.22154e-102
NZ_CP033687.1\|WP_061565731.1\|470122_471154_-\|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_CP033687.1\|WP_046720946.1\|456550_457174_+\|histidine-phosphatase-family-protein	gnl\|CDD\|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.01398e-69
NZ_CP033687.1\|WP_061577465.1\|472680_474561_-\|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.	5.54126e-178
NZ_CP033687.1\|WP_035183676.1\|457945_458365_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	1.4066e-15
NZ_CP033687.1\|WP_026684593.1\|471150_471807_-\|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.	4.39067e-31
NZ_CP033687.1\|WP_017552101.1\|481740_482328_+\|nitroreductase-family-protein	gnl\|CDD\|380315	cd02138, TdsD-like, nitroreductase similar to Burkholderia pseudomallei TdsD. A subfamily of the nitroreductase family containing uncharacterized proteins that are similar to Burkholderia pseudomallei TdsD, may be involved in the processing of organosulfur compounds. Nitroreductase catalyzes the reduction of nitroaromatic compounds such as nitrotoluenes, nitrofurans and nitroimidazoles. This process requires NAD(P)H as electron donor in an obligatory two-electron transfer and uses FMN as cofactor. The enzyme is typically a homodimer.	2.92291e-75
NZ_CP033687.1\|WP_026684592.1\|471796_472657_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl\|CDD\|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. 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; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	2.89273e-134
NZ_CP033687.1\|WP_017551458.1\|451758_452673_-\|DUF1002-domain-containing-protein	gnl\|CDD\|377628	pfam06207, DUF1002, Protein of unknown function (DUF1002). This protein family has no known function. Its members are about 300 amino acids in length. It has so far been detected in Firmicute bacteria and some archaebacteria.	4.74261e-82
NZ_CP033687.1\|WP_035183662.1\|474561_475281_-\|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.	6.65501e-99
NZ_CP033687.1\|WP_026684595.1\|469821_470112_-\|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.	1.60661e-36
NZ_CP033687.1\|WP_046720947.1\|450854_451736_+\|hypothetical-protein	gnl\|CDD\|227596	COG5271, MDN1, AAA ATPase containing von Willebrand factor type A (vWA) domain [General function prediction only].	0.00244629
NZ_CP033687.1\|WP_110134170.1\|447961_449497_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.01506e-19

>NZ_CP033687.1|WP_110134131.1|467184_468600_-|ISLre2-like-element-ISBco6-family-transposase
MDIISIIAGLLKDTKSLIEFEEQLKLLMQKAFTQWVGEIFEELDKIIKQEKLEEGWVYCRSDNRNIQFLFGSVTFKRSLMHDKRGNSHYPLDEWLGLVPHQRYSPLVELKVAELASENTYREVADILKEWTAVSLSHTTVGNMVKHVGKTQAEADKALVEELEIAVSLPEGKKVDYLFSEADGVFVRGLKKKQSMEVHHAILYEGWQTNGKRVSLRQPTVIMTTEAIQTFWDEVQATAANTYSLEKTHVITNSDGGAGYTAERFQTAFSQSEFPVLNQLDTYHVAQAIIRTFGGGKSEIKEQIRKAIRTHDLDQFTLYLDTHESTLTDKKALKKIKEFRSYILKNWDRIFDWRDRVKNVPEGARGLGAMESNQRHISFRMKKRGMHWSELGAEAMVKIKQGILNGTLREAYLKHRSRSERKQRNLKQFIRMSQLLKQPVRPSVGVKHGSVALHSSSSSAMGHLSKILELSF
>NZ_CP033687.1|WP_035183676.1|457945_458365_+|helix-turn-helix-transcriptional-regulator
MADHGNENMENVKEIFAARLKKVRTAQGYSQPELAKKVGVSDRNISNYETGYSFPSIKVLYRISQVLKVSIDYLLGLTNHAGLKTNEAVSNPEKKLLETLSHEPDLYQMMLKDPEKMANRIYQTWNLIRELDDEDDRNT
>NZ_CP033687.1|WP_046720946.1|456550_457174_+|histidine-phosphatase-family-protein
MTLFYFVRHGQTEWNADRNRYCGRSDIGLSQTGVRQAELAAGFLKDIPFNAVYASTLGRAARTAEILVEGRNLKIYQDPRLVETDFGAWEGERQEDFSVKYADNWEAWLKDPGATHAGYTGETAVQVYQRVRACIDELVEKHPEETVLVVAHSMAIRFFVAGTLEVPFKNYRMIPQDNTGITIYKETPENAGFLAINLNTHLSSIKS
>NZ_CP033687.1|WP_110134171.1|454583_455891_-|cation:dicarboxylase-symporter-family-transporter
MKRVSLAWQIFIGLILGIAIGGIFHGNDTVAHILQPFGDFFLRLIKMIVIPIVVSSLIVGVAGAGDMKQVGKLGLKALIYFEIVTTIAIVVGLLAGNLFHPGTGVDMGSLAKTSISSYVETTKETQHNGIVDTILSIVPTNLFESLSQGNMLPIIFFSVMFGIGVAAIGEKGKPVLRFFQGVSEAMFYVTNLVMKVAPIGVFGLIGVTVTQFGLKSLIPLSKLVFTVYGTIIFFVVVVLGLIAWLFRVNIFNLFKILKDELILAYSTASSEAVLPRLMEKMEKFGCPKSITTLVIPTGYSFNLDGSTLYQSLAALFIAQMYGIHMSIGAQISLVLVLMVTSKGIAGVPGVSFVVLLATLGTVGIPLEGLAFIAGIDRILDMARTACNVVGNTLATIIVSKWEGKYDKEKAEAYLAEISGGGHDTDAKDHKYVTES
>NZ_CP033687.1|WP_026684954.1|453059_454205_-|metallophosphoesterase
MDKKMLLWVAVLSLALFPRTEHADAAFWFQSKRATVDLRLLETSDLHGYMLNYDYAARTEAETYGLALTASLIAAERKTAKNTMLFDDGDLLEGNEMAAYVARRPLKKGEIHPFIRVMNHLNYDAATVGNHDFHYGLDFLKQTINGAKFPFVNANIYYNFEKNDTDDQNFFKPYVILDKKVEDRSGHHHHLKIGVIGFVTPSVIEWEKPSLGGKVKAKDILHTAAWFVPRMKAEGADLIIALAHCGVDPAAKQPFYTGDAVYLLSEVKGIDAILFGHQHRVFPSEFFAGVPGVDIRKGTINGVPAVMPGKWGSHLGVISLTLEKKGEKWEMTQAQSEAKPVYAIHNQQAKSIVRPDPDIVRMTAELQKNVLGSKFTLYSRN
>NZ_CP033687.1|WP_017551458.1|451758_452673_-|DUF1002-domain-containing-protein
MLKRLGWIWFIAMIALGFTMNGVAKASGDNSTVIDEKYGKPIVATGAALSASQKAEVEKELGVDDANNVEEITVTGDDLVHYIPDGNRNSNMYSSAKITRTDSGGIQVNIVTPENITEVTADMYKNALLTAGIKNAEVEVASPLKVTGHSALVGIYKAYDNSDKSGDKLNSDRTEVASQELSVATDLAKKEGLSNDQVTQLLTEIKQEIANQHPATKEDIEKIVDDKLKDLNINLSDSDRQLLYDLFDQMRKLNINFGSVKSELSSLSDKLSDKINKAAGDKDFWQSVKDFFQNIFDAIRGLFQ
>NZ_CP033687.1|WP_046720947.1|450854_451736_+|hypothetical-protein
MVRQVKKTKSFLLTAAFIAFNFCFFTNISVAESPVTDGFIIEADRVEGAMLPPGITAGDTATKQNQVMLRLQYADVTIYGLKITKVLQTPEGPVTIHMNAPGPIQLKNMRVDATKVNFGGIYVPEKARQIGMKNVRLVAHQQLADNADLPGLNLSMETGAADIDTSGSDEETLRKQADQLTQLLQGGTPEKNKEEKNDKSDTADKAKDGTQDKAKTEKQDTEKHNDAKTDGKVTDQNKNKESENTDDTKLDNTGTEPASGQETEKNRTTTKTAQDQSSTDQNVQQKEGSSAEN
>NZ_CP033687.1|WP_017551460.1|450416_450839_+|hypothetical-protein
MGKFHMFRMKFRNWRRSRPFWGATFTLLSGMIILYVPVQLLEIAAAPGSMVSIGLIFGGLIFLIGGMGYFFPKFNMVFGILAIFLSVLSIMGAMGGFFIGTLLGIIGGSLSVSWRVIRQEEVPAGVGPMEEIAAGSAEER
>NZ_CP033687.1|WP_014097216.1|449783_450392_+|hypothetical-protein
MNEGALVLQGQGRTSKKWFFTALLSGLIFLGGLLAVLGINGVAVAATVGGIGKFNVSFKQMQGTGFKLYGSLYGDPSKGEDHVKPVFVNEIDKVTIQDLVISKDVKIPVLGDYQVKITAGDGNTPVHLNGLIQKAALVQGDAVFTNMNISENYVTADDPQAASKAFTQGADTLTIKNGSLDTHYLFQKVANLPNLKVQFVKK
>NZ_CP033687.1|WP_110134170.1|447961_449497_-|helix-turn-helix-transcriptional-regulator
MSLSLNAHMDMVMKHGVDLLRSHQQQIIAECTGILQYLGETHKGSADAFEFAFNCFVAFFRSGQQSVETLIDDIRSQWVKEFHRPPEPHVLIFILTLIENSVHKAIKESTTRSFHLHPSVQYLFSKICEEMLLISKQETFQMDSFCEQLTKSEQLRIEWIARVSHVDGGYRLKKVIGMEENAIDSGLFERTDPSWFWLSEALLKRTPRRKPDERRDVFPVPWKNETLIFCMSDQDVSATIPFLTYAMHLLQMEEERNGKVYAGDQWKDAVILFNEWIMRSQDLNEAIQNIAFGYAQYLPFERCALFRYSQSDAAGFGLFGYHFNNTAIRNIKETIDRFPSISKILLGKGQQVNMVQHFQPLYIPKASEEFPMQYVKEFELESVVVAPIYVPSEGVLIGGAILDQGPGKFFEVDSSTFTALLKFGQSAGELLAKFLKANQWDEKQPELVQLSAREIHILQLLADGASTTEAAEMLHLSEYTVRDYVSSLMKRLHARNRTEAAVKAMRLGLIH
>NZ_CP033687.1|WP_026684595.1|469821_470112_-|CRISPR-associated-endonuclease-Cas2
MLVVITYDVSTLTGAGQKRLRKVAKVCQNYGQRVQNSVFECFVDATQFASLKIELSNIIDPDEDSLRFYQLGNNYKNKVMHIGAKPSLDLEDPLIF
>NZ_CP033687.1|WP_061565731.1|470122_471154_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLLNTLFITQPEVYLSLDGDNIVLLKEKEQLGRLPLHNLESVVAFGYTGVSPALMGYCAERNISLIFFTMNGRFLARVIGKSRGNVVLRKKQYRISDDEIASVQIARNFIIGKIYNQKWILERMTRDYPLRIDVTQFKDVSRFLSAIIKQVRLCDSLETLRGLEGQAAINYNKLFDQMILQQKDDFFFHHRSRRPPLDNVNAMLSFAYTLLANDTASALEGVGLDAYVGFMHQDRPGRVSLALDLMEELRGVYADRFVLSLINTKVINKDDFLKKENGTVIMTDEARKKFLKAWQNKKQEKITHPFLGEKISWGLVPHAQALLLARFLRGDLDEYPPFLWK
>NZ_CP033687.1|WP_026684593.1|471150_471807_-|CRISPR-associated-protein-Cas4
MAFDEDEYLMLSGIQHFQFCKRQWALIHIEQAWEENVRTVEGQNIHQKTDSPFIREKRGSKLIVRAMPIKSNELKLTGICDVVEFVKDKNGVEIYGNEGKYIPYPVEYKRGKPKKNDSDILQLVAQAMCLEEMLLCEVNKGYIFYNEIKRRIEIPITLDEKNKVRKIAAEMQDYYQRRYTPKVKTGPFCNQCSLQNICLPNIIRKRAVSSYIEGKINE
>NZ_CP033687.1|WP_026684592.1|471796_472657_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MSALDHKIDFAVVLSVTKANPNGDPLNGNRPRQNYDGYGEISDVAIKRKIRNRLQDMGESIFVQSNDRKNDSYNSLKERADANPELNKIFKSKDGSGETFAAIACQEWIDVRSFGQVFAFKGSGNKGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDFGVYVLYGSINPQLAEKTGFSNEDAEKIKQALVTLFENDASSARPEGSMEVKKVYWWEHQSKLGQYSSAKVHRSLAVTPLVDNPKTFEDYEITLNELSGLKVDVIDGI
>NZ_CP033687.1|WP_061577465.1|472680_474561_-|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQANEEQVGKIEKKRNDQEYTLLPVSHTTQTAHLEVQVTEDGNFYYAEVINDKKDAVTLIPCTEESSSRAGKKIAPYPLHDKLIYVAGDFVAYGGKIEEPFSYYIQQLGEWANSPFSNAKVQSIYAYLKKKQLIHDLVEAGILFLDNNGQLIDKWDSKYGDKPPLYSTVTGSVESAFVRFTVYSPEKILTKVWKDPEMYESFIKFYNQHLSDRDLCYVTGEFLPSTERHANKIRNSGDKAKLISANDSSGFTYRGRFTESKQVASISYKASQKAHNALKWLINKQGKIIDNRVFLVWENGGNEVPSVTEDSYDITSLDPFANGNNPKIAFTNQEFAREFSKAMDGYKSNLSTEASINILVLDSATTGRMAVLYYRNLNKEIYFENLVKWHTTCAWLHRYRKNEDNQPILFFGAPATKDIAFAAYGPNASDKVVKGLMERMLPCIVEGRRIPTDIVRSALRRASNPVALEKWEWEKILSIACALINKEEGYNLALDKENNNRDYLFGRLLAIADVFERNALDSGENRATNAIRYMNAFSQHPARTWGTIQASLQPYQVRLGKKGTYYAMLIDEVASKLKYEDFNDRPLSGKFLLGFYSQRYDLYQKKETNTVGQTKE
>NZ_CP033687.1|WP_035183662.1|474561_475281_-|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFEVYGKYALFTDPLTKMGGEKLSYQIPTYQALKGIVESIYWKPTILMIIDDLRVMNPIKMESKGVRPIEYNGGNTLANYTYLRDVRYKVRAHFIFNPHRPDLAFDRNEHKHHNILKRSLKAGGRRDIFLGARECQGYVEPCVFEEGEGYYDQTEEVYFGTMVHGINYPDETGRNEMEVRLWNPVMKNGVIHFIRPDECKLVRRVAEMEMKAFTKDNVESADVLLKELERGGEL
>NZ_CP033687.1|WP_110134172.1|475478_477905_-|CRISPR-associated-helicase-Cas3'
MEYIAHIRESDKKVQTVEEHLLAAKELAETYGEKIGVKHITGLAALLHDLGKYTSAFRNYILEAVNNPDHPPKRGSVDHSTAGGKLLFKMFHSGKASPHKALLTEIVGNAIISHHSYLQDFISPEMDLKYLNRVDSKEIDEFETAKENFFEKVMSPTRFSSYVNQAEIELKNFIMKDASKTLTHKMMFLTKYIFSALIDADRTNTRLFEENKPKKEQFPVSKLFNQYYEKLLLTLDSYKENSSANARINRLRSEMSEQCDAFAEKPSGIYTLSIPTGGGKTFASLRYALKHAQLYNKKRIIYIVPFTTIIEQNAEEVRKVLQDDVNILEHHSNVVEDADENDEQQDGIMSVQQRLKLAKDNWDVPIIFTTMVQFLNVFYAKGSRNIRRLHNMSEAVLIFDEVQKVPVPCISLFNEALNFLKTYCHSSILLCTATQPALNYVEHQLQVSPNPEIIRGLDNVIDAFKRVEIVDRATDETFNTEKLANFIEKRMTEVSSVLVILNTKGVVKKLYEHLNSNDNNINIFHLSTSMCAAHRNQILEEVRHCLDAGKKVICVSTQLIEAGVDVSFECVIRSLAGLDSIAQAAGRCNRHGEKETGFVYVINHEEENLSRLPEIKKGKETSKRIFIDLKNTPSIYNGNVLSIQAMEKYFKEFYTAFDANLDYNVPSLQKNMVEMLTTDPNNYSYVRAYCSNTKKKYPLFLSSSFYTAAEKFRVIDDKTTSVIVPFGKGNDVIAELSSNATIEDLSKLMKKAQQYTINLYSQELGKLERNGGIISLFDGKILALKEGAYDHEFGLNVENDSELDFLSI
>NZ_CP033687.1|WP_142010191.1|478039_478234_-|hypothetical-protein
MGLSARIARMLQVSRLREAFADALNKVFAAFSKDASGLPIARLSLPREMAGYIKENYLVGTFPA
>NZ_CP033687.1|WP_110134173.1|478351_481591_-|DEAD/DEAH-box-helicase-family-protein
MVDYLLFEEDVEMMYSPAIFHRGMSYYMQGRVKKLIFNKDSTWTAIVKGSKTYYVTIYYDEEFGEFSNVCTCPAHEQYGECKHEVAAMLAIANGEEEAAEPNIGDVSETHQHMKTLQLMNIFSGLQQSMMETKHNAARKPLRLEYFLKATNVSGFGSDHFLTIEIKIGPGRTYVVRDIKDFLGNVSRGNPHAFTKNFIYDPDEHAFEEEDKEIVEMLLYMLSTQQLYEASMDRWYRFALERELVIPPFIARPLIKKLANRKCKFKYERYAADSIVLHQEEELPLSFRLDGNSQGGPGFLLQLKSLRDLLLFEQYGLAFYKGGFYELSTDQLALLTALEDFYKKSGDEVEIQQEQMSPFLSNVLPGLKRIGKVKLTKDIKGKIVQPKLQTKIFMDNEDEKITLRIEHHYGSRVIDPFMDEETPDDDKILLRDVEKEQKIMTMIEQSPLKYNGKQLYLENDEEALYEFIFTILPQLEEEAEVYIAGAIKSYFQTSHYTPLTSVDMDTSGNFLEVNFDMDGIDEEEIRNVLRSVIEKKRYYRLPDGAFVSLESDEFEHIGQLLGELHVSKKELEDTRLKVPLYRGLQVEELMKTRDKYAVKFGKAFRKLVQQLKNPEDTDFELPKGLEAKMRDYQVTGFQWFKSLAFYRLGGILADDMGLGKTLQSISYMLSEKEANPDIKPFLVVAPASLIYNWKSEIEKFAPGLSSMVIAGTPSERKAFFEAGELPDVLITSYPTLRQDIEEYEKIEFDTLILDEAQAIKNYATKTAAAVRNVQAGRRFALSGTPIENSIDELWSIFQAVLPGFFPPLPEFRKMEQEKISRMVRPFILRRVKKDVLKELPDKIETNHLSELTKPQKELYLAYLDRIRHETAQTLAEGDFNRNRIKILAGLTRLRQLCCHPSLFVENYRGDSGKLEQLVELAHTAIENGKRLLIFSQFSSMLQMIRTRLSDEGIDSFYLDGQTPSRERVEMADRFNSGEKNVFLISLKAGGTGLNLTGADTVVLYDLWWNPAVEEQAAGRAHRIGQKNVVQVIRLIARGTIEEKIYELQQKKKELIEQVIQPGETMLNSLNEEEIKELLGM
>NZ_CP033687.1|WP_017552101.1|481740_482328_+|nitroreductase-family-protein
MVKTLSPREAQYDIDPVYLERWSPRSFLEKEVPEEVLLSLFEAARWAPSAYNHQPWRFILARTKEDREKVLSFLGEYNRMWCKNVPAFALILSKTENETGPIRSHAFDAGAAWGYLSLEAVRKGLATHPMTGFDFEKAREVLNIPSDYAIDALIAIGYRGEKEALPPSLQERETPSARRPVKESVFEGSFGNPVK

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Crispr_ID: NZ_CP033687_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_5

1116263-1116353

Orphan

Consensus_repeat	Method
CCATATAATAAAAAAGCACTCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_5

>merge|NZ_CP033687|5|1116263-1116353|CRISPRCasFinder
CCATATAATAAAAAAGCACTCGATGGGCTACATAGCTTGAACAGGCACGAAATCGGGGGTTAGGTGAACCATATAATAAAAAAGCACTACG

>NZ_CP033687|5|5|1116263-1116353|CRISPRCasFinder
CCATATAATAAAAAAGCACTCGA	TGGGCTACATAGCTTGAACAGGCACGAAATCGGGGGTTAGGTGAA
CCATATAATAAAAAAGCACTACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_013860883.1\|1123501_1123741_-\|30S-ribosomal-protein-S18	unknown	unknown	gnl\|CDD\|178997
NZ_CP033687.1\|WP_026683519.1\|1110541_1111336_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|224156
NZ_CP033687.1\|WP_014096624.1\|1120394_1122368_-\|DHH-family-phosphoesterase	unknown	unknown	gnl\|CDD\|226404
NZ_CP033687.1\|WP_014096622.1\|1123785_1124280_-\|single-stranded-DNA-binding-protein	unknown	unknown	gnl\|CDD\|168659
NZ_CP033687.1\|WP_026683518.1\|1111352_1112135_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378229
NZ_CP033687.1\|WP_014096628.1\|1115226_1115937_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP033687.1\|WP_014096621.1\|1124341_1124629_-\|30S-ribosomal-protein-S6	unknown	unknown	gnl\|CDD\|179034
NZ_CP033687.1\|WP_014096619.1\|1125365_1126559_-\|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|181774
NZ_CP033687.1\|WP_035183097.1\|1108284_1108764_-\|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH	unknown	unknown	gnl\|CDD\|376840
NZ_CP033687.1\|WP_026683520.1\|1109062_1110325_-\|PDZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|273938
NZ_CP033687.1\|WP_026683523.1\|1104922_1106443_-\|SAM-dependent-DNA-methyltransferase	unknown	unknown	gnl\|CDD\|223363
NZ_CP033687.1\|WP_017550648.1\|1106459_1107053_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|376540
NZ_CP033687.1\|WP_014096629.1\|1113401_1115222_-\|cell-wall-metabolism-sensor-histidine-kinase-WalK	unknown	unknown	gnl\|CDD\|380161
NZ_CP033687.1\|WP_026683517.1\|1112121_1113405_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369363
NZ_CP033687.1\|WP_142010210.1\|1122403_1123345_-\|YybS-family-protein	unknown	unknown	gnl\|CDD\|370773
NZ_CP033687.1\|WP_014096626.1\|1118379_1119735_-\|replicative-DNA-helicase	unknown	unknown	gnl\|CDD\|180232
NZ_CP033687.1\|WP_014096627.1\|1116915_1118205_-\|adenylosuccinate-synthase	unknown	unknown	gnl\|CDD\|234904
NZ_CP033687.1\|WP_104851698.1\|1108705_1108903_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014096625.1\|1119954_1120398_-\|50S-ribosomal-protein-L9	unknown	unknown	gnl\|CDD\|234659
NZ_CP033687.1\|WP_014096620.1\|1124882_1125353_-\|6,7-dimethyl-8-ribityllumazine-synthase	unknown	unknown	gnl\|CDD\|234606

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_013860883.1\|1123501_1123741_-\|30S-ribosomal-protein-S18	gnl\|CDD\|178997	PRK00391, rpsR, 30S ribosomal protein S18; Reviewed.	6.9465e-42
NZ_CP033687.1\|WP_026683519.1\|1110541_1111336_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|224156	COG1235, PhnP, Metal-dependent hydrolases of the beta-lactamase superfamily I [General function prediction only].	1.30136e-70
NZ_CP033687.1\|WP_014096624.1\|1120394_1122368_-\|DHH-family-phosphoesterase	gnl\|CDD\|226404	COG3887, COG3887, Predicted signaling protein consisting of a modified GGDEF domain and a DHH domain [Signal transduction mechanisms].	0
NZ_CP033687.1\|WP_014096622.1\|1123785_1124280_-\|single-stranded-DNA-binding-protein	gnl\|CDD\|168659	PRK06751, PRK06751, single-stranded DNA-binding protein; Provisional.	9.81725e-74
NZ_CP033687.1\|WP_026683518.1\|1111352_1112135_-\|hypothetical-protein	gnl\|CDD\|378229	pfam09648, YycI, YycH protein. This domain is exclusively found in YycI proteins in the low GC content Gram positive species. These two domains share the same structural fold with domains two and three of YycH pfam07435. Both, YycH and YycI are always found in pair on the chromosome, downstream of the essential histidine kinase YycG. Additionally, both proteins share a function in regulating the YycG kinase with which they appear to form a ternary complex. Lastly, the two proteins always contain an N-terminal transmembrane helix and are localized to the periplasmic space as shown by PhoA fusion studies.	4.02054e-56
NZ_CP033687.1\|WP_014096628.1\|1115226_1115937_-\|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].	4.68549e-100
NZ_CP033687.1\|WP_014096619.1\|1125365_1126559_-\|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II	gnl\|CDD\|181774	PRK09311, PRK09311, bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II.	0
NZ_CP033687.1\|WP_035183097.1\|1108284_1108764_-\|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH	gnl\|CDD\|376840	pfam02590, SPOUT_MTase, Predicted SPOUT methyltransferase. This family of proteins are predicted to be SPOUT methyltransferases.	3.9983e-88
NZ_CP033687.1\|WP_026683520.1\|1109062_1110325_-\|PDZ-domain-containing-protein	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	6.69913e-92
NZ_CP033687.1\|WP_026683523.1\|1104922_1106443_-\|SAM-dependent-DNA-methyltransferase	gnl\|CDD\|223363	COG0286, HsdM, Type I restriction-modification system methyltransferase subunit [Defense mechanisms].	7.12427e-155
NZ_CP033687.1\|WP_017550648.1\|1106459_1107053_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|376540	pfam01381, HTH_3, Helix-turn-helix. This large family of DNA binding helix-turn helix proteins includes Cro and CI. Within Neisseria gonorrhoeae NGO_0477, the full protein fold incorporates a helix-turn-helix motif, but the function of this member is unlikely to be that of a DNA-binding regulator, the function of most other members, so is not necessarily characteristic of the whole family.	1.435e-05
NZ_CP033687.1\|WP_014096629.1\|1113401_1115222_-\|cell-wall-metabolism-sensor-histidine-kinase-WalK	gnl\|CDD\|380161	NF033092, HK_WalK, cell wall metabolism sensor histidine kinase WalK. This model describes WalK as found in Staphylococcus aureus (sp\|Q2G2U4.1\|WALK_STAA8). A shorter version, as found in Streptococcus pneumoniae, called WalK(Spn) or VicK, is not included. WalK is part of a two-component system and works with partner protein WalR.	0
NZ_CP033687.1\|WP_026683517.1\|1112121_1113405_-\|hypothetical-protein	gnl\|CDD\|369363	pfam07435, YycH, YycH protein. This family contains the bacterial protein YycH which is approximately 450 residues long. YycH plays a role in signal transduction and is found immediately downstream of the essential histidine kinase YycG. YycG forms a two component system together with its cognate response regulator YycF. PhoA fusion studies have shown that YycH is transported across the cytoplasmic protein. It is postulated that YycH functions as an antagonist to YycG. The molecule is made up of three domains, and has a novel three-dimensional structure. The N-terminal domain features a calcium binding site and the central domain contains two conserved loop regions.	3.5023e-79
NZ_CP033687.1\|WP_142010210.1\|1122403_1123345_-\|YybS-family-protein	gnl\|CDD\|370773	pfam09991, DUF2232, Predicted membrane protein (DUF2232). This family of bacterial proteins are multi-pass membrane proteins with up to 10 (2 x 4/5) transmembrane regions. The exact function of this potential pore molecule is not known, but in many instances it is associated with ABC-transporter-like domains, implying that it is part of a secretion system that uses energy.	1.59343e-42
NZ_CP033687.1\|WP_014096626.1\|1118379_1119735_-\|replicative-DNA-helicase	gnl\|CDD\|180232	PRK05748, PRK05748, replicative DNA helicase; Provisional.	0
NZ_CP033687.1\|WP_014096627.1\|1116915_1118205_-\|adenylosuccinate-synthase	gnl\|CDD\|234904	PRK01117, PRK01117, adenylosuccinate synthetase; Provisional.	0
NZ_CP033687.1\|WP_014096621.1\|1124341_1124629_-\|30S-ribosomal-protein-S6	gnl\|CDD\|179034	PRK00453, rpsF, 30S ribosomal protein S6; Reviewed.	1.01619e-40
NZ_CP033687.1\|WP_014096625.1\|1119954_1120398_-\|50S-ribosomal-protein-L9	gnl\|CDD\|234659	PRK00137, rplI, 50S ribosomal protein L9; Reviewed.	9.80627e-66
NZ_CP033687.1\|WP_014096620.1\|1124882_1125353_-\|6,7-dimethyl-8-ribityllumazine-synthase	gnl\|CDD\|234606	PRK00061, ribH, 6,7-dimethyl-8-ribityllumazine synthase; Provisional.	6.10782e-87

>NZ_CP033687.1|WP_014096628.1|1115226_1115937_-|response-regulator-transcription-factor
MDKKILVVDDEKPIADILQFNLTKEGYTVYCAYDGEEALEKVEEVQPDLIVLDIMLPKRDGMEVCREVRKKYNMPIIMVTAKDSEIDKVLGLELGADDYVTKPFSTRELIARVKANLRRHQQTPAAPGEEEESNEIAIGSLVIHPDAYVVSKRGETIELTHREFELLHYLAKHIGQVMTREHLLETVWGYDYYGDVRTVDVTVRRLREKVEDNPSHPEWIVTRRGVGYYLRNPEQE
>NZ_CP033687.1|WP_014096629.1|1113401_1115222_-|cell-wall-metabolism-sensor-histidine-kinase-WalK
MNKVKFFQSIHFKFVLIYILLIVVAMEIIGVYFINKLENQLETNFKKSIYDQVNVLEYSIEDLLTKKQNQAADITLKVRKVLGDFKSTDVSEIRLIDAHSGVILGTSSNDQSIVGQKTTEDIVKSVRVTGQPEDQIYLDKQTGDRMWVLASPIKANGELIGIIYLVSKIETVYRQVQAINQIFMTGTVIAVLVTALLGIITARTISKPLSEIRKQAMAMARGNFARKVKVIGNDEIGQLAYSFNHMTKKLQEAQASTEGERRKLDSILTHMTDGVIATDRRGRIILINEPAAEMLDVSRETVLSQPLISVLKIENEHKFDDLLTEQDSVILDFSTEEEPYILRANFSVIQNEAGFVSGLITVLHDVTEQEKIDMERREFVANVSHELRTPLTTMRSYLEALTDGAWKDEKIAPQFLGVTQNETERMIRLVNDLLKLSKMDSKDEHLNKEWVNFVEFFHHVIDRFEMAKQQNVTFKRKLPNTEIFVEIDEDKMTQVLYNIISNALKYSPEGGQITFKLRELNEKIEVSISDQGVGIPKENVKKIFERFYRVDKARSRKLGGTGLGLAIAKEMVEMHGGSIWASSKEGKGTTIYFTLPYEPAQEDEWL
>NZ_CP033687.1|WP_026683517.1|1112121_1113405_-|hypothetical-protein
MSLEKAKTIILTLLVLLSLLLTWLIWNNQPNYDLLNLKDLDNIAIAKEKKVPGIILPDKILYHENDGTTGTVHDGEISRVMNLLRTWTFDMSSSRLLQKKDLYNLMYGKNRIELDFPAPVPFSVYQSVLNFANKKVPDADFDHIVIELNKGTKNLNHVYFISTASNKVYEASTDQKSIQVFISKLNDNKSLYKPYTAFALSGPRRIYLPAGNPVVNQYKYATTDIEIDKFKKALFADPNFVKKVAGEYTNGISLLRTDESNKVLTFVNPGEDIGYSSDPNHLLTRAIDFINQHSGWTDQYQYFEINERENEVTFRLFKDGYPVFNDDGMAEIREYLGKSEIYKYVRPYFNLSLNLTLKPAAVKLPPAQDVIAGLQTNPSVQMNKVRDIAVGYRLQKDSDDILSLQPAWYYCEDGIWKMAGGDEDGLE
>NZ_CP033687.1|WP_026683518.1|1111352_1112135_-|hypothetical-protein
MDWSKTKTIFILVFLVLDIYLSCQLYFKHVKNQYEVIGSPTAEQSLKAANITFVNLPKGKAKRPYISAEEKVFTAKDLKKLKNQQAEIVNGYQLSSAFDKPVKLGTKIKTDQLEAVIQENMLYGSRYKLWNYDKDLNQAVFYETYNGKMIFNNKNAKLTVYLNDQNEIISYDQTYLTNIKIYREEEETLSAVKAVEALYKKGTLKPNSKVTKAELGYYTRVPELQVLVPTWHFTVKHGNETEQLFINAFEGQVNEMENAQ
>NZ_CP033687.1|WP_026683519.1|1110541_1111336_-|MBL-fold-metallo-hydrolase
MGMQFSVLASGSTGNAIYVETEQHAFLVDAGLSGRQMEQLFGQIGRNIADLSGILVTHEHSDHIKGIGVLARKYKLPIYANDKTWSAMEGMIGEIPTDLKFSFGMESVQSFGSLEIESFGVSHDAVQPMFYIFHEGSKKLVIITDTGYVSDRMKGTISNADIFVFESNHDVEMLRMGRYPWSVKQRILSDVGHVSNEDAALAMSEVIGDRTKRIYLAHLSKDNNMKDLARMAVSQTLQEQGLAVGETFSLYDTDPKIPTALTAV
>NZ_CP033687.1|WP_026683520.1|1109062_1110325_-|PDZ-domain-containing-protein
MGYYDDQDGQRRGKENRRSGGKFGYFLSGLIGVIVGALVVALLFPNIFGKTNSDSSAVDSNSVANTSTSTAKTTKTVSLKVTTDITKAVEKTEKAVVGVSNIQKQSIWSDDMFGQDSKSSSSSSQEAGSGSGIIYKKAGDKAYVVTNYHVIEGANALEVTLSNGKKLSAKLVGGDKYTDLAVLQIDGSNVTTVAQFGDSDALKLGESVIAIGNPLGEEFAGSVTEGIVSGLNRTVPVDIDEDGTEDWQEEVIQTDAAINPGNSGGALINISGQVVGINSMKISNESVEGIGFSIPINSAKPVIHQLETKGKITRPAMGVGIVNVSDISAYQQQETLKLPTNVTTGVVIGSIENGSPAGKAGLKEFDVIYKLDDQKINNTVELRKYLYEHKQPGDKVKVSVYRNGQPKTFTLTLGTASGSN
>NZ_CP033687.1|WP_104851698.1|1108705_1108903_+|hypothetical-protein
MPCFKYFSFNFPTVTIEIFTTYTHLTHKLLTRVIHISTETIHILCGNNRSIQDIFHHFSLFTACL
>NZ_CP033687.1|WP_035183097.1|1108284_1108764_-|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH
MNISIVTVGKLKEKYLKQGIQEYLKRLSAYAKVEIIEVADEKASEMLSAAEMELVKQKEGERILAKISPDTYVITLAIDGKMKSSEELADSLDRLATYGKSKIAFVIGGSLGLSQAVLQRGNESLSFSKMTFPHQLMRLILVEQIYRAFRIIRGEPYHK
>NZ_CP033687.1|WP_017550648.1|1106459_1107053_-|helix-turn-helix-domain-containing-protein
MIGLEYILELYGMQQIELAEKLGIKKQNINLWIKRKQKISKKHLPTLEQIFGIDAKYFSKELTDLDKLEIQKEKLKRDLQPIITKYEEQFLIGEENDLVEVPVYDKEELNQIEHDIEKAKLIEKFRNMLNRAEHQPYLDTFKLVLELLDKAQHEPVFHKTIEALAHYLEVLPDWVSTGPEQDEFESELFEVLDDFNY
>NZ_CP033687.1|WP_026683523.1|1104922_1106443_-|SAM-dependent-DNA-methyltransferase
MMETAKIGFEETLWKSADKLRGSMDASEYKHVVLGLIFLKYISDKFEMKYNELVEEGEGFEEDRDEYTAENIFWVPKQSRWSFIKDRAKDPKIGQYIDEAMIEIEKENPSLRGVLDKRYARPEIDKRRLGELIDLISTIKLHSKQEKDLLGRVYEYFLGKFASAEGKGGGEFYTPQSVVKTLVEMIEPYEGRIYDPCCGSGGMFVQSEKFVERHQGKIDNLSIYGQELNSTTWKLCKMNLAIRGIEGNIGEHHADTFHNDLHKTLKADFILANPPFNVSDWGGNELVDDVRWKFGTPPASNANYAWLQHMIYHLSPNGAAGIVLANGSLSSNTSNEGEIRKNILEADLVDAIVALPDKLFYSTGIPVSLWILNRNKKNHPKYRSREHEILFIDARNMGQMVDRRLRELTEEDIQKIAGTYRNWRKPDGKYEDIKGFCKSATLEDVRQNDYVLTPGRYVGISDVEDDGIPFEEKMETLTSELRELFEKSHRLEEEIRKNLGGIGYEI
>NZ_CP033687.1|WP_014096627.1|1116915_1118205_-|adenylosuccinate-synthase
MSSVVVVGTQWGDEGKGKITDFLSENAEVVSRYQGGNNAGHTIRFNGETYKLHLIPSGIFYKDKICVIGNGVVVDPKALVEELDYLNGRGISTENLRISNRAHVILPYHIKLDGAEEERKGSNKIGTTKKGIGPAYMDKAARTGIRIADLLDYEEFKEKLTRNLEEKNRLFEKIYETEGFTLEEILEPYYEYGQRFKQYVCDTSVVLNDALDAGKRVLFEGAQGVMLDIDQGTYPFVTSSNPIAGGVTIGSGVGPSKINHVVGIAKAYTTRVGDGPFPTELLDETGDRIRETGHEYGTTTGRARRVGWFDSVVVRHARRVSGLTDLSVNLLDVLTGIETLKICVAYRYKGKVLEAFPASLKVLAECEPVYEELPGWTEDITGCRSLDELPDNARHYLERISQLTGVPLSMFSVGPDRLQTIVVQSVWRV
>NZ_CP033687.1|WP_014096626.1|1118379_1119735_-|replicative-DNA-helicase
MNELQDRIPPQNIEAEQAVLGAIFLEPSAFITASEILTAEDFYRNAHQKIFQVFAKLNDAGKAVDLVTVAEELSATRQLEDAGGLSYLSELAASVPTAANIAYYAGIVAEKALLRRLIRTATHIAQEGYTREDDVDELLDEAERSIMEVAQRKNAGDFKHIKDVLVSTYDNIEMLHNRKGDVTGIPTGFYELDRMTAGFQRNDLIIVAARPSVGKTAFALNIAQNVGTKTEENVAIFSLEMGAEQLVMRMLCAEGNIDAQRLRTGALTDEDWRKLTMAMGSLSNSGIYIDDTPGVRVTEIRSKCRRLKQEHGLGMVVIDYLQLIQGSARSRENRQQEVSEISRSLKALARELEVPVIALSQLSRGVEQRQDKRPMMSDIRESGSIEQDADIVAFLYREDYYEQDTENKNIIEIIIAKQRNGPVGTVQLAFIKEYNKFVNLERRFDDAPVPA
>NZ_CP033687.1|WP_014096625.1|1119954_1120398_-|50S-ribosomal-protein-L9
MKVIFLKDVKGKGKKGDIKNVADGYAHNYLFKNGAAIEATPANLKSMEAQKRKEEKLAQEELEEAKKLKEKLENITVEIKAKSGQDGRLFGSVTSKQISEQLKKSFQIQVDKRKIELPDAIRTLGYTKVPVRLHHNVTAVLNVHVSE
>NZ_CP033687.1|WP_014096624.1|1120394_1122368_-|DHH-family-phosphoesterase
MPSYYNKRFMRYPLYGLIAVSLILLGIIFFYHWWITAAGIVVLGALSYCAFYVEQRSSEEIERYISNLSYRVKRVGEEALMEMPIGIMLYNEDYIIEWTNPFMASCFNEDTLVGRSLYDVAEVLVPLIKQEMHSETISLNERKYRVVLKLEERLLYFFDITEQAEVEQLYEDERTVIAIIYLDNYDEVTQGMDDQSVSSLNSLVTSILNKWTMEFGLFFKRISSDKFIAVFNERILHELEDNKFSILDEVREATAKQNVALTLSIGVGAGVPSLPELGELAQSSLDIALGRGGDQVAIRQANGKVKFYGGKTNPVEKRTRVRARVISHALRELMMERDKVMIMGHKFPDMDAIGAAVGIRKVAEINQKDGYIILNPSETDTSVKRLLGEIKQYPDLYARFITPDEALEMATDDTLLVVVDTHKPSLVIDERIVRRIENVVVIDHHRRGEDFIKNPLLVYMEPYASSTSELVTELMEYQPKNGKINMLEATALLAGIIVDTKSFTLRTGSRTFDAASYLRAQGADTVLVQKFLKEDLRSYIQRAKLVETVKFPLNGIAVAKGKNDTIYSPVLMAQAADTILMMNGVDASFVIGRRSENEVGISARSLGSVNVQIIMETLDGGGHLSNAATQMKNITVDEAEEKLIQVIEEYMEGSQQS
>NZ_CP033687.1|WP_142010210.1|1122403_1123345_-|YybS-family-protein
MKKTRMLTEGAMLAAVFGVMLLVALHVPVIRIIVLVFLPLPFILFCAKYSLRSILVFCLVCLLVSAIMGTVMAIPMAVFFVCIGFVMGYAIQRKKSKLFIYIATSLTFLAITIIGLFATLKFFHLNIIAENLKIMQQSIEQSKALVNSLGESQAYEDRFAQMADVASQMYSVYLPSLLLLSAFIAVFVLISVNFPIAKRFGVPVPSFQPFREMRLPGNILWYFILAMVANLLMHGDTGSFFAKAVLNLMLIFQILILLQGYAFISFVSHEKKWPKGLLAFAVILSIIFSPLLYLVMIFGIMDLGFDFRRMIQK
>NZ_CP033687.1|WP_013860883.1|1123501_1123741_-|30S-ribosomal-protein-S18
MAGGRRGGRKRRKVCYFTANHITHIDYKDVDLLKKFISERGKILPRRVTGTSAKYQRKLTTAIKRARQMALLPYVAEDK
>NZ_CP033687.1|WP_014096622.1|1123785_1124280_-|single-stranded-DNA-binding-protein
MLNRVVLVGRLTKDPDLRYTPSGVAVATFTLAVNRTFTNQQGEREADFINCVVWRKQAENVANYLKKGSLAGVDGRIQTRNYEAQDGRRVYVTEVVADSVQFLEPRSANQERGSSQNYGNNQGSAFPGYNQNQNQYQRNDSKPDEDPFSNDGQPIDISDDDLPF
>NZ_CP033687.1|WP_014096621.1|1124341_1124629_-|30S-ribosomal-protein-S6
MRKYEIMYIIRPNIEDEAKKALVERFDNVLNNQGAEIIESKEWGKRRLAYEIQDFRDGYYHIINVNAEPVAVQEFDRLAKINGDIIRHIVVREEE
>NZ_CP033687.1|WP_014096620.1|1124882_1125353_-|6,7-dimethyl-8-ribityllumazine-synthase
MGQIFEGNLVGTGLKIGMVAARFNEFITTRLVSGAKDALLRHGVKEEAIDLAWVPGAFEIPLAAKKMAETDKYDAVLALGAVIRGATPHFEYVSAEAAKGVAHASLSTETPVIFGILTTDTIEQAIERAGTKAGNKGWDAAVSAIEMANVIRKIEA
>NZ_CP033687.1|WP_014096619.1|1125365_1126559_-|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II
MFHTIEEAVEDLKAGKVVIAVDDENRENEGDFIGLAEKATPEMINLMAKAGRGLICAPITAEKAQQLDLYPMARQNTDSHETAFTVSIDHAATRTGISAFERAKTVRHLAEDAVKAEDFHRPGHIFPLVAKAGGVLERSGHTEAAVDLAKLAGANPAGVICEIMNEDGTMARLPQLEEIAKNSGIKLVTIQSLIEYRKKHEKLIQKEAEITLPTRYGTFRAAGYKDLLSGGEHVALIKGEVSSEEPVLARIHSECLTGDCFGSLRCDCGPQLARSLARIEKEGRGVLVYMRQEGRGIGLLNKLKAYRLQEKGLDTVEANRRLGFPADMRDYCIAAQILKDLGATQVRLLTNNPDKVEALTRYGIRIAERVPVEIAPVRENEGYLRTKAEKMGHLLHI

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Crispr_ID: NZ_CP033687_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_6

1262698-1262788

Orphan

Consensus_repeat	Method
CCCGTCTTTTGCTGGAACAAGCATA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_6

>merge|NZ_CP033687|6|1262698-1262788|CRISPRCasFinder
CCCGTCTTTTGCTGGAACAAGCATAGCCTGGCGGGGGCACTCGTGGTACAGTGGCAATTCCATTATCCCGTCTTTTGCTGGAACAAGCATA

>NZ_CP033687|6|6|1262698-1262788|CRISPRCasFinder
CCCGTCTTTTGCTGGAACAAGCATA	GCCTGGCGGGGGCACTCGTGGTACAGTGGCAATTCCATTAT
CCCGTCTTTTGCTGGAACAAGCATA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_014096529.1\|1254602_1255670_+\|protein-arginine-kinase	unknown	unknown	gnl\|CDD\|234894
NZ_CP033687.1\|WP_142010216.1\|1251654_1252179_+\|CPBP-family-intramembrane-metalloprotease	unknown	unknown	gnl\|CDD\|376806
NZ_CP033687.1\|WP_013858048.1\|1253576_1254038_+\|CtsR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|226869
NZ_CP033687.1\|WP_014096519.1\|1266856_1267270_+\|Mini-ribonuclease-3	unknown	unknown	gnl\|CDD\|224850
NZ_CP033687.1\|WP_014096525.1\|1260086_1261172_+\|PIN/TRAM-domain-containing-protein	unknown	unknown	gnl\|CDD\|227292
NZ_CP033687.1\|WP_017551231.1\|1269550_1269697_+\|50S-ribosomal-protein-L33	unknown	unknown	gnl\|CDD\|234783
NZ_CP033687.1\|WP_014096530.1\|1254057_1254603_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226397
NZ_CP033687.1\|WP_026684125.1\|1262950_1264411_+\|glutamate--tRNA-ligase	unknown	unknown	gnl\|CDD\|234953
NZ_CP033687.1\|WP_014096524.1\|1261238_1261919_+\|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase	unknown	unknown	gnl\|CDD\|234670
NZ_CP033687.1\|WP_110133723.1\|1250273_1251590_+\|streptolysin-associated-protein-SagD	unknown	unknown	gnl\|CDD\|274674
NZ_CP033687.1\|WP_035182978.1\|1258369_1259740_+\|DNA-repair-protein-RadA	unknown	unknown	gnl\|CDD\|236994
NZ_CP033687.1\|WP_014096528.1\|1255686_1258137_+\|ATP-dependent-Clp-protease-ATP-binding-subunit	unknown	unknown	gnl\|CDD\|214361
NZ_CP033687.1\|WP_014096515.1\|1269732_1269918_+\|preprotein-translocase-subunit-SecE	unknown	unknown	gnl\|CDD\|236066
NZ_CP033687.1\|WP_026684122.1\|1268014_1268524_+\|NYN-domain-containing-protein	unknown	unknown	gnl\|CDD\|226213
NZ_CP033687.1\|WP_014096514.1\|1270067_1270601_+\|transcription-termination/antitermination-protein-NusG	unknown	unknown	gnl\|CDD\|180161
NZ_CP033687.1\|WP_014096521.1\|1264813_1265482_+\|serine-O-acetyltransferase	unknown	unknown	gnl\|CDD\|223975
NZ_CP033687.1\|WP_014096520.1\|1265462_1266860_+\|cysteine--tRNA-ligase	unknown	unknown	gnl\|CDD\|234705
NZ_CP033687.1\|WP_014096523.1\|1261921_1262398_+\|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase	unknown	unknown	gnl\|CDD\|376811
NZ_CP033687.1\|WP_014096518.1\|1267269_1268013_+\|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB	unknown	unknown	gnl\|CDD\|129290
NZ_CP033687.1\|WP_081092958.1\|1268590_1269241_+\|RNA-polymerase-sporulation-sigma-factor-SigH	unknown	unknown	gnl\|CDD\|181361

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_014096529.1\|1254602_1255670_+\|protein-arginine-kinase	gnl\|CDD\|234894	PRK01059, PRK01059, ATP:guanido phosphotransferase; Provisional.	0
NZ_CP033687.1\|WP_142010216.1\|1251654_1252179_+\|CPBP-family-intramembrane-metalloprotease	gnl\|CDD\|376806	pfam02517, Abi, CAAX protease self-immunity. Members of this family are probably proteases (after a isoprenyl group is attached to the Cys residue in the C-terminal CAAX motif of a protein to attach it to the membrane, the AAX tripeptide being removed by one of the CAAX prenyl proteases). The family contains the CAAX prenyl protease. The proteins contain a highly conserved Glu-Glu motif at the amino end of the alignment. The alignment also contains two histidine residues that may be involved in zinc binding. While they are involved in membrane anchoring of proteins in eukaryotes, little is known about their function in prokaryotes. In some known bacteriocin loci, Abi genes have been found downstream of bacteriocin structural genes where they are probably involved in self-immunity. Investigation of the bacteriocin-like loci in the Gram positive bacteria locus from Lactobacillus sakei 23K confirmed that the bacteriocin-like genes (sak23Kalphabeta) exhibited antimicrobial activity when expressed in a heterologous host and that the associated Abi gene (sak23Ki) conferred immunity against the cognate bacteriocin. Interestingly, the immunity genes from three similar systems conferred a high degree of cross-immunity against each other's bacteriocins, suggesting the recognition of a common receptor. Site-directed mutagenesis demonstrated that the conserved motifs constituting the putative proteolytic active site of the Abi proteins are essential for the immunity function of Sak23Ki - thus a new concept in self-immunity.	0.000722886
NZ_CP033687.1\|WP_013858048.1\|1253576_1254038_+\|CtsR-family-transcriptional-regulator	gnl\|CDD\|226869	COG4463, CtsR, Transcriptional repressor of class III stress genes [Transcription].	7.71878e-73
NZ_CP033687.1\|WP_014096519.1\|1266856_1267270_+\|Mini-ribonuclease-3	gnl\|CDD\|224850	COG1939, COG1939, Ribonuclease III family protein [Replication, recombination, and repair].	5.97073e-61
NZ_CP033687.1\|WP_014096525.1\|1260086_1261172_+\|PIN/TRAM-domain-containing-protein	gnl\|CDD\|227292	COG4956, COG4956, Integral membrane protein (PIN domain superfamily) [General function prediction only].	3.9088e-178
NZ_CP033687.1\|WP_017551231.1\|1269550_1269697_+\|50S-ribosomal-protein-L33	gnl\|CDD\|234783	PRK00504, rpmG, 50S ribosomal protein L33; Validated.	3.43221e-14
NZ_CP033687.1\|WP_014096530.1\|1254057_1254603_+\|hypothetical-protein	gnl\|CDD\|226397	COG3880, COG3880, Modulator of heat shock repressor CtsR, McsA [Signal transduction mechanisms].	3.16274e-59
NZ_CP033687.1\|WP_026684125.1\|1262950_1264411_+\|glutamate--tRNA-ligase	gnl\|CDD\|234953	PRK01406, gltX, glutamyl-tRNA synthetase; Reviewed.	0
NZ_CP033687.1\|WP_014096524.1\|1261238_1261919_+\|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase	gnl\|CDD\|234670	PRK00155, ispD, D-ribitol-5-phosphate cytidylyltransferase.	4.8734e-112
NZ_CP033687.1\|WP_110133723.1\|1250273_1251590_+\|streptolysin-associated-protein-SagD	gnl\|CDD\|274674	TIGR03604, hypothetical_protein, thiazole/oxazole-forming peptide maturase, SagD family component. Members of this protein family include enzymes related to SagD, previously referred to as a scaffold or docking protein involved in the biosynthesis of streptolysin S in Streptococcus pyogenes from the protoxin polypeptide (product of the sagA gene). Newer evidence describes an enzymatic activity, an ATP-dependent cyclodehydration reaction, previously ascribed to the SagC component. This protein family serves as a marker for widely distributed prokaryotic systems for making a general class of heterocycle-containing bacteriocins.	5.30027e-85
NZ_CP033687.1\|WP_035182978.1\|1258369_1259740_+\|DNA-repair-protein-RadA	gnl\|CDD\|236994	PRK11823, PRK11823, DNA repair protein RadA; Provisional.	0
NZ_CP033687.1\|WP_014096528.1\|1255686_1258137_+\|ATP-dependent-Clp-protease-ATP-binding-subunit	gnl\|CDD\|214361	CHL00095, clpC, Clp protease ATP binding subunit.	0
NZ_CP033687.1\|WP_014096515.1\|1269732_1269918_+\|preprotein-translocase-subunit-SecE	gnl\|CDD\|236066	PRK07597, secE, preprotein translocase subunit SecE; Reviewed.	2.34704e-14
NZ_CP033687.1\|WP_026684122.1\|1268014_1268524_+\|NYN-domain-containing-protein	gnl\|CDD\|226213	COG3688, COG3688, Predicted RNA-binding protein containing a PIN domain [General function prediction only].	3.74279e-75
NZ_CP033687.1\|WP_014096514.1\|1270067_1270601_+\|transcription-termination/antitermination-protein-NusG	gnl\|CDD\|180161	PRK05609, nusG, transcription antitermination protein NusG; Validated.	6.48023e-95
NZ_CP033687.1\|WP_014096521.1\|1264813_1265482_+\|serine-O-acetyltransferase	gnl\|CDD\|223975	COG1045, CysE, Serine acetyltransferase [Amino acid transport and metabolism].	5.02969e-103
NZ_CP033687.1\|WP_014096520.1\|1265462_1266860_+\|cysteine--tRNA-ligase	gnl\|CDD\|234705	PRK00260, cysS, cysteinyl-tRNA synthetase; Validated.	0
NZ_CP033687.1\|WP_014096523.1\|1261921_1262398_+\|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase	gnl\|CDD\|376811	pfam02542, YgbB, YgbB family. The ygbB protein is a putative enzyme of deoxy-xylulose pathway (terpenoid biosynthesis).	8.76229e-103
NZ_CP033687.1\|WP_014096518.1\|1267269_1268013_+\|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB	gnl\|CDD\|129290	TIGR00186, Uncharacterized_tRNA/rRNA_methyltransferase_MG252, rRNA methylase, putative, group 3. this is part of the trmH (spoU) family of rRNA methylases [Protein synthesis, tRNA and rRNA base modification].	5.28043e-99
NZ_CP033687.1\|WP_081092958.1\|1268590_1269241_+\|RNA-polymerase-sporulation-sigma-factor-SigH	gnl\|CDD\|181361	PRK08295, PRK08295, RNA polymerase sporulation sigma factor SigH.	1.24151e-119

>NZ_CP033687.1|WP_014096523.1|1261921_1262398_+|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase
MFRIGQGFDVHRFGEGRPLMIGGVEIPYEKGLLGHSDADVLLHAVADACLGAIGEGDIGRHFPDTDAAFKDADSAALLAHVFQLVKQKGYKLGNLDCTIIAQKPKMAPYIGKMRETIARILEAEIGQVNVKATTTEKLGFAGREEGIAAQAAVLLEQA
>NZ_CP033687.1|WP_014096524.1|1261238_1261919_+|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase
MTDYEVIIPAAGSGKRMGAGFNKLFLELNKRPVIAVTAEVFLADPSCKKLILPVQPHDREEMKRILPRSEKIVFARGGSERQYSVRNGLELAGSCSVILVHDGARPFISAGSIAALAAMAGEKGAAIAAVPVKDTIKRAKDQIVTETIERSSLWQIQTPQAFRTSVLKKAHEAAERDGFLGTDEASLVERIGHPVHIVPGSYDNIKITTPEDLYFAEAILKKQGGG
>NZ_CP033687.1|WP_014096525.1|1260086_1261172_+|PIN/TRAM-domain-containing-protein
MLLRRLIQICLVLIGGTLGVFLLPDFYKLVKVDYVLINNPYVSALLGAIIFYLITFWSIHYIVDFVDWFEDSLVKVPMTEIFSGTFGLVLGLIIAYLASIPVRGIPIVNTIVSITLTVLLGYIGFQVGFKKREEIFNLFFNRQHRRKGGTEQEGHPQPGKQVKILDTSVVIDGRIADICQTGFLDGPIVIPLFVLEELQHIADSSDALKRNRGRRGLDILNRIQNELPIEVQMYEGDFEDIQEVDSKLIKLAKLMNGIVVTNDYNLNKVCEFQKVKVLNINDLANAVKPVVLPGEELNVQLIKDGKEHHQGIAYLDDGTMIVVEEGKNYIGKRIDVLVTSVLQTSAGRMIFAKPKLLEKAL
>NZ_CP033687.1|WP_035182978.1|1258369_1259740_+|DNA-repair-protein-RadA
MAKKTVKFVCQNCGYESPKWMGKCPQCSQWNQMVEEAETPKRRGFFLHPEPGNETKAAPITSIESKEEKRTKVDFGELNRVLGGGIVAGSLVLIGGDPGIGKSTLLLQVSSQLAKHGLNVLYISGEESAKQTKLRADRLNIHTDHLYVLPETDLSVIQQAIDELNPGFVVIDSIQTIYHPEIQSAPGSVSQVRETTAQLMRTAKTKNVAIFIVGHVTKEGSIAGPRVLEHMVDTVLYFEGERHNAYRILRAVKNRFGSTNEIAILEMKESGLEEVQNPSEIFLEERTKGAAGSTVVASIEGTRPVLVEIQALLAPTFFNMPRRMASGIDYNRVTLIMAVLEKRAGLLIQNQDAYLKVAGGLKVDEPAVDLAVAVSVASSFRDKPTNADDCIIGEVGLTGEVRRVSRIEQRVQEAAKLGFRRAIIPKNNMGGWTPPKEIQVIGVSTIQEALQAALGG
>NZ_CP033687.1|WP_014096528.1|1255686_1258137_+|ATP-dependent-Clp-protease-ATP-binding-subunit
MMFGRFTERAQKVLALSQEEAIRLKHNNIGTEHILLGLVREGEGIAAKALYGLGLSAEKIQEEVETLIGNGQEISQTIHYTPRAKKVIELSMDEARKLGHSYVGTEHILLGLIREGEGVAARVLTNLGVSLNKARQQVLQLLGNSEASVQGGSAASVSTPTLDSLARDLTAIAREDSLDPVIGRSKEIQRVIEVLSRRTKNNPVLIGEPGVGKTAIAEGLAQQIVHNEVPETLRDKRVMTLDMGTVVAGTKYRGEFEDRLKKVMDEIRQAGNIILFIDELHTLIGAGGAEGAIDASNILKPSLARGELQCIGATTLDEYRKYIEKDAALERRFQPIQVDEPTIDESIQILKGLRDRYEAHHRVSITDEAIEAAVKLSDRYIADRFLPDKAIDLIDEAGSKVRLRSFTTPPNLKELELKLEEVRKEKDAAVQSQEFEKAAALRDTEQKLREQLEETKKNWKAKQGQENSEVTVDDIALVVSSWTGVPVTKLAQTETERLLHLEEILHSRVIGQEEAVLAVAKAVRRARAGLKDPKRPIGSFIFLGPTGVGKTELARALAEAMFGDEDAMIRIDMSEYMEKHSTSRLVGSPPGYVGFEEGGQLTEKVRRKPYSVVLLDEIEKAHPDVFNILLQVLDDGRLTDSKGRTVDFSNTIVIMTSNVGADALKRNKSVGFTIQDTVEADYKDMKDKVLEELKKAFRPEFLNRVDETIVFHSLEKKQLNEIVTLMAKELSDRLKEHHIELVLTDAAKEKVAEKGYDPEYGARPLRRSIQKNIEDRLSEEMLKGNIKEGQKVLVDVKDGEFTFASVAESEAVSSNS
>NZ_CP033687.1|WP_014096529.1|1254602_1255670_+|protein-arginine-kinase
MSLEHFLHKASSSWMNEQGPESEIVLTTRVRLARNLKNYRFPSLFTSEEAREIMKTIQDIARNHFPAEMQAEFLKMDELKPLEKRVLVEKHLISPQLAEEAGDGAVILSSGEDISIMINEEDHLRIQCLSPGLQLHETLQKANQLDDLLENWVDYAFDETLGYLTSCPTNVGTGIRASAMMHLPGLVLTQQIKQIIPAIHQLGLVVRGIYGEGSEAIGNIFQISNQVTLGTSEDNIVSDLTSVIRQIITQERSAREALVQTSNIQLEDRVYRSLGVLQNSRIIETKEAARCLSDVRLGIDLGYIQNISKQILNELMILMQPGFLQLYAGRALSPYERDIRRATLIRERLRLEETK
>NZ_CP033687.1|WP_014096530.1|1254057_1254603_+|hypothetical-protein
MICQECNERPATMHFTKIINGVKTEFHLCEKCAQEKGEKFSSDWGKTFSFDNLLAGLFNFDPAIQLFKQETAPDPDVLRCNHCGMTLNQFLNTSRLGCPHCYETFQHQLVPILQRLHGGNVAHEGKIPARIGGAIYTKKKLQELKAALQEAISQEEFEKAAELRDQIRALEGSSQAKGGEQ
>NZ_CP033687.1|WP_013858048.1|1253576_1254038_+|CtsR-family-transcriptional-regulator
MKNISDIIEEYLKRILELNEKEILEIKRNEIADKFQCVPSQINYVINTRFTIERGYIVESKRGGGGYIRIMKVRPESDAELIDQLLVHIGNVISQSNAEAIILRLVEEEVISRREAKIMLSVMDRSVLYIQLPERDELRARMLKSMLTTLKYK
>NZ_CP033687.1|WP_142010216.1|1251654_1252179_+|CPBP-family-intramembrane-metalloprotease
MRYQSSFEQYSLTLIFVIIINFFALRLPSLMLIELMTLAIIPAFLFIIESLLKNQQFGLFFFYKKYNLTAFIAIVIYPVLEEMNFRYFVYQYGQSFGYSTLQYIILSSLVFTMSHVIAQGASSNYKLLFAFVQALIYVIFMNIYINIIIHIIFNVFVYFNKLEFNSGLQNKQKF
>NZ_CP033687.1|WP_110133723.1|1250273_1251590_+|streptolysin-associated-protein-SagD
MIKIENTPGYNHMRKDILGGNVTGIWANNSFFIGANSFPVMNYHYLTAKYNNFEKNLFENDQKINYHLSGYGTLYNETLTSFLGESSERYSYTALYTNIKKFIVKSSYEQLKQRFPDDLVCDLEIINSYFSPQDKENYIDEKDEITWMPMNSLIETGKRTFIPLQLLVMFDQEIFKNEKRYITSSVSTGTASQETFEESVESAIIEYLQIDSFNIWWYSGFEGLKLDLDIKQKLRKWFNNQFLINEFIRNFQITFSDISLDKDIFVILCEVTAKKEGLPKYVIGVQGGYNLEKCIYRSFMECVTVLEYAFNIVWIDPSKFKNIGTDVQKLEIDNLDDNIIFYAKTGKPNRKTRKFPYNQTDREKINNLPMLIKSLKRFSKYAGVLCITPPEFKKMNLFISRVVIPELLPIALPFYPPYYHKRYRMLGGIINHLPHPLA
>NZ_CP033687.1|WP_026684125.1|1262950_1264411_+|glutamate--tRNA-ligase
MANEIRVRYAPSPTGFLHIGNARTALFNYLFARSKGGKFIIRIEDTDQKRNVEGGVESQLKYLKWLGIDWDESIDVGGEYGPYRQSERLDIYKKYYEDLLDRGLAYKCYCTEEELEAEREAQLARGEMPRYSGKCRHLTEEDRKRLEAEGRKPSIRFHVPEGKVYTFNDIVKGEVSFESDGIGDFVIVKKDGMPTYNFAVTIDDHLMKMSHVLRGDDHISNTPKQLMIYEAFGFEPPVFGHMTLIVNEHRKKLSKRDGSIIQFIEQYAELGYLPEALFNFIAMLGWSPKGEEEIFSREEFIQIFDPERLSKSPALFDRQKLAWMNNQYMKKLDLDKVVELALPHLVKAGLVPENRTPEEEQWVRKLISLYQEQMSYGAEIVELSKPLFFTDEITYDDEAKAILSGEHVPEVLRAFLEELDRIEPFEAGEIKKAIKAVQKATGQKGKKLFMPIRVAVSGQTHGPELQSLIELLGREKVKKRLERITG
>NZ_CP033687.1|WP_014096521.1|1264813_1265482_+|serine-O-acetyltransferase
MFKRLKEDIEVVFDQDPAARTYFEVILTYSGLHAIWAHRIAHFFYKKKMFFIARVISQLSRFFTGIEIHPGAQIGRRFFIDHGMGVVIGETCEIGDNVTVYQGVTLGGTGKEKGKRHPTIKDNALIASGAKVLGSITIGENAKIGAGSVVLKDVPPNSTVVGIPGRVVVQDGVKIKKDLKHNELPDPVADRLNSMQQEIEALRSELEQLRKEGARMYEHSDI
>NZ_CP033687.1|WP_014096520.1|1265462_1266860_+|cysteine--tRNA-ligase
MSIQIYNTLTRKKEPFIPLEEGKVKMYVCGPTVYNYIHIGNARPAIVFDTVRRYLAFRGYDVNYVSNFTDVDDKLIKAAKERGEEVPALSERFIKSYFEDIDALGCCHADAHPRVTENMDAIIAFIEKLIEKGHAYESGGDVYYHTRSFPDYGKLSHQSIDELKSGARIEVGEKKEDALDFALWKAAKEGEISWDSPWGKGRPGWHIECSAMAKKYLGDTIDIHAGGQDLTFPHHENEIAQSEALTDKPFARYWMHNGYINIDNEKMSKSLGNIVLVHDIIERHDPQVLRFFMLSVHYRHPINYSEELLANAKAGLERIKTSYQNVKHRLESSANLAEDDEKWLEQVRSLHRQFIEAMDDDFNTANGISVLFELSKQANYYLRGKNTTETVLRAFMKEFETISGVLGLKLEEEVLLDEEIEALIEKRNEARKARNFQLADEIRDKLKSMNIILEDTPQGVRWRRL
>NZ_CP033687.1|WP_014096519.1|1266856_1267270_+|Mini-ribonuclease-3
MTVTLDPKQLNSLALAYMGDAVYEEYIRHHVLLQGKTKPNRLHREAIRFVSAKAQAQILKQMMNENLLTEEETAVVRRGRNAKSGTVPKNTDVQTYRHSTAFEALIGYHYLSGSRERMEALIKKAIDIVEDQKGGAH
>NZ_CP033687.1|WP_014096518.1|1267269_1268013_+|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB
MDQEYIAGKNPVLEALRAGREINKIWIAEGSQKGAMKQVIELARERKVTVQFVPKKKIDQVADGAHQGVLALVAAYRYAETGDMFKLAKERNEHPFILILDELEDPHNLGSILRTADAVGAHGVIIPKRRSVALTATVAKASTGAIEHIPVARVTNLSQTIAGLKQQGLWIAGTDASGTTDYRQMDADLPLCLVIGSEGKGMSRIVKEACDFLIRLPMAGHVTSLNASVAAGLLMYEVYRKRHPLGE
>NZ_CP033687.1|WP_026684122.1|1268014_1268524_+|NYN-domain-containing-protein
MNILLVDGYNIIGAWPELQKLKQKDLGAARDRLVEIMAEYQGYTDDKVIVVFDAYGVKGLEKKYRYHKVEVIFTKENETADERIEKMAIKLNNIRTQIYVATSDFTEQWQIFGQGALRISARELLTKVEMIEQKIKKNVKSIQEEKPATRIPLSQEVMEIFEKLRRGKR
>NZ_CP033687.1|WP_081092958.1|1268590_1269241_+|RNA-polymerase-sporulation-sigma-factor-SigH
MNLNIEAAYEERYGTMQDEELVGRIHNGESEALDYLIQKYRNFVRAKARSYFIIGADREDIIQEGMIGLYKAIRDYREDKLTSFKAFAELCINRQMITAIKTATRQKHIPLNSYISLDKPIYDEESDRTLMDVITGAKISNPEELILIREKYVHIEVKISELLSDLERKVLALYLDGQSYQEISEELNRHVKSIDNALQRVKKKLERLLEMRELTY
>NZ_CP033687.1|WP_017551231.1|1269550_1269697_+|50S-ribosomal-protein-L33
MQKKMVLACSVCGSRNYTTTTGNGKAERMELKKFCKHCNEHTIHRGTK
>NZ_CP033687.1|WP_014096515.1|1269732_1269918_+|preprotein-translocase-subunit-SecE
MSITNFFRNVASEMRKVSWPGRKELVKYTITVLVTVAFLTLFFIVIDLGISAVIRWAENSL
>NZ_CP033687.1|WP_014096514.1|1270067_1270601_+|transcription-termination/antitermination-protein-NusG
MEKNWYVVHTYSGYENKVKTNLEKRVESMGMQDKIFRVVVPEEEELEVKNEKKKVVKRKVFPGYVLVEMVMTDDSWYVVRNTPGVTGFVGSSGGGSKPTPLLPEEINTILKRMGMEEKRADVDFEIGETVTVKEGPFANFAGKIVEMDRDKGRAKVMVNMFGRDTPVELVFEQIDKI

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Crispr_ID: NZ_CP033687_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_7

1603124-1603468

Orphan

Consensus_repeat	Method
TTTGTCCTTTTGACAGGTTCAAAAGGACATTTC	CRT

6 spacers

The CRISPR arrays of NZ_CP033687_7

>merge|NZ_CP033687|7|1603124-1603468|CRT
TTTGTCCTTTTGACAGGTTCAAAGGGACATTTCATTCCCGGATGCGGCATGTTTTGTCCTTTTGACAGGTTCAAAAGGACATTTCGGGCCCGGATGCAGCTCGTTTTGTCTTTTTGACGGCTTCAAAAGGACATTTCGGGCCCGGATGCAACTCCTTTTGTCCTTTTGACAGGTTCAAAAGGACATTTCGTTACCTGATGCAGCTCGTTTTGTCTTTTTGACGGCTTCAAAAGGACATTTTGGGCCCGGATGCAATTCCTTTTGTCCTTTTGACAGGTTCAAAAGGACATTTCATTCCCGGATGCGGCACGTTTTGTCCTTTTGACAGGTTCAAAAGGACATTTC

>NZ_CP033687|7|3|1603124-1603468|CRT
TTTGTCCTTTTGACAGGTTCAAAGGGACATTTC	ATTCCCGGATGCGGCATGT
TTTGTCCTTTTGACAGGTTCAAAAGGACATTTC	GGGCCCGGATGCAGCTCGT
TTTGTCTTTTTGACGGCTTCAAAAGGACATTTC	GGGCCCGGATGCAACTCCT
TTTGTCCTTTTGACAGGTTCAAAAGGACATTTC	GTTACCTGATGCAGCTCGT
TTTGTCTTTTTGACGGCTTCAAAAGGACATTTT	GGGCCCGGATGCAATTCCT
TTTGTCCTTTTGACAGGTTCAAAAGGACATTTC	ATTCCCGGATGCGGCACGT
TTTGTCCTTTTGACAGGTTCAAAAGGACATTTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_014097040.1\|1607910_1609326_+\|ISLre2-like-element-ISBco6-family-transposase	unknown	unknown	gnl\|CDD\|284250
NZ_CP033687.1\|WP_014096261.1\|1612381_1613197_+\|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270407
NZ_CP033687.1\|WP_026684940.1\|1611088_1611817_+\|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224051
NZ_CP033687.1\|WP_017551739.1\|1607083_1607269_+\|twin-arginine-translocase-TatA/TatE-family-subunit	unknown	unknown	gnl\|CDD\|237837
NZ_CP033687.1\|WP_142010224.1\|1598739_1599444_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_035182624.1\|1598317_1598791_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_061087274.1\|1589502_1591131_+\|glycerol-3-phosphate-dehydrogenase/oxidase	unknown	unknown	gnl\|CDD\|223651
NZ_CP033687.1\|WP_013858270.1\|1606072_1606909_-\|undecaprenyl-diphosphate-phosphatase	unknown	unknown	gnl\|CDD\|234712
NZ_CP033687.1\|WP_110133769.1\|1591401_1592670_+\|C4-dicarboxylate-transporter-DctA	unknown	unknown	gnl\|CDD\|234968
NZ_CP033687.1\|WP_014096259.1\|1613941_1614649_+\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP033687.1\|WP_014096260.1\|1613262_1613916_+\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP033687.1\|WP_017551743.1\|1614823_1615225_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224639
NZ_CP033687.1\|WP_013858263.1\|1595639_1596176_-\|YceI-family-protein	unknown	unknown	gnl\|CDD\|225228
NZ_CP033687.1\|WP_061087273.1\|1597055_1598174_-\|NADH-dependent-flavin-oxidoreductase	unknown	unknown	gnl\|CDD\|240086
NZ_CP033687.1\|WP_014096278.1\|1592975_1593656_+\|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223736
NZ_CP033687.1\|WP_035182628.1\|1594582_1595287_-\|iron-sulfur-cluster-repair-di-iron-protein	unknown	unknown	gnl\|CDD\|274701
NZ_CP033687.1\|WP_110133772.1\|1609722_1610748_+\|AI-2E-family-transporter	unknown	unknown	gnl\|CDD\|223701
NZ_CP033687.1\|WP_026684984.1\|1601522_1602905_+\|glycine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235240
NZ_CP033687.1\|WP_061565278.1\|1599992_1601015_+\|HD-GYP-domain-containing-protein	unknown	unknown	gnl\|CDD\|225116
NZ_CP033687.1\|WP_110133771.1\|1604087_1605908_+\|APC-family-permease	unknown	unknown	gnl\|CDD\|372624

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_014097040.1\|1607910_1609326_+\|ISLre2-like-element-ISBco6-family-transposase	gnl\|CDD\|284250	pfam06782, UPF0236, Uncharacterized protein family (UPF0236).	3.22884e-48
NZ_CP033687.1\|WP_014096261.1\|1612381_1613197_+\|transporter-substrate-binding-domain-containing-protein	gnl\|CDD\|270407	cd13689, PBP2_BsGlnH, Substrate binding domain of ABC glutamine transporter from Bacillus subtilis; the type 2 periplasmic-bindig protein fold. This group includes periplasmic glutamine-binding domain GlnP from Bacillus subtilis and its related proteins. The GlnP 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.	3.70304e-93
NZ_CP033687.1\|WP_026684940.1\|1611088_1611817_+\|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].	5.70829e-167
NZ_CP033687.1\|WP_017551739.1\|1607083_1607269_+\|twin-arginine-translocase-TatA/TatE-family-subunit	gnl\|CDD\|237837	PRK14861, tatA, twin arginine translocase protein A; Provisional.	4.34295e-21
NZ_CP033687.1\|WP_017551743.1\|1614823_1615225_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|224639	COG1725, COG1725, Predicted transcriptional regulators [Transcription].	7.17288e-40
NZ_CP033687.1\|WP_061087274.1\|1589502_1591131_+\|glycerol-3-phosphate-dehydrogenase/oxidase	gnl\|CDD\|223651	COG0578, GlpA, Glycerol-3-phosphate dehydrogenase [Energy production and conversion].	0
NZ_CP033687.1\|WP_110133769.1\|1591401_1592670_+\|C4-dicarboxylate-transporter-DctA	gnl\|CDD\|234968	PRK01663, PRK01663, C4-dicarboxylate transporter DctA; Reviewed.	0
NZ_CP033687.1\|WP_014096259.1\|1613941_1614649_+\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	4.22326e-69
NZ_CP033687.1\|WP_014096260.1\|1613262_1613916_+\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	1.17854e-68
NZ_CP033687.1\|WP_013858263.1\|1595639_1596176_-\|YceI-family-protein	gnl\|CDD\|225228	COG2353, COG2353, Uncharacterized conserved protein [Function unknown].	6.33719e-62
NZ_CP033687.1\|WP_061087273.1\|1597055_1598174_-\|NADH-dependent-flavin-oxidoreductase	gnl\|CDD\|240086	cd04735, OYE_like_4_FMN, Old yellow enzyme (OYE)-related FMN binding domain, group 4. Each monomer of OYE contains FMN as a non-covalently bound cofactor, uses NADPH as a reducing agent with oxygens, quinones, and alpha,beta-unsaturated aldehydes and ketones, and can act as electron acceptors in the catalytic reaction. Other members of OYE family include trimethylamine dehydrogenase, 2,4-dienoyl-CoA reductase, enoate reductase, pentaerythriol tetranitrate reductase, xenobiotic reductase, and morphinone reductase.	0
NZ_CP033687.1\|WP_014096278.1\|1592975_1593656_+\|Crp/Fnr-family-transcriptional-regulator	gnl\|CDD\|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	4.65303e-44
NZ_CP033687.1\|WP_035182628.1\|1594582_1595287_-\|iron-sulfur-cluster-repair-di-iron-protein	gnl\|CDD\|274701	TIGR03652, FeS_repair_RIC, iron-sulfur cluster repair di-iron protein. Members of this protein family, designated variously as YftE, NorA, DrnN, and NipC, are di-iron proteins involved in the repair of iron-sulfur clusters. Previously assigned names reflect pleiotropic effects of damage from NO or other oxidative stress when this protein is mutated. The suggested name now is RIC, for Repair of Iron Centers. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	4.44798e-94
NZ_CP033687.1\|WP_110133772.1\|1609722_1610748_+\|AI-2E-family-transporter	gnl\|CDD\|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	2.87926e-41
NZ_CP033687.1\|WP_110133771.1\|1604087_1605908_+\|APC-family-permease	gnl\|CDD\|372624	pfam13520, AA_permease_2, Amino acid permease.	1.89373e-32
NZ_CP033687.1\|WP_026684984.1\|1601522_1602905_+\|glycine--tRNA-ligase	gnl\|CDD\|235240	PRK04173, PRK04173, glycyl-tRNA synthetase; Provisional.	0
NZ_CP033687.1\|WP_061565278.1\|1599992_1601015_+\|HD-GYP-domain-containing-protein	gnl\|CDD\|225116	COG2206, COG2206, c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms].	8.57971e-55
NZ_CP033687.1\|WP_013858270.1\|1606072_1606909_-\|undecaprenyl-diphosphate-phosphatase	gnl\|CDD\|234712	PRK00281, PRK00281, undecaprenyl-diphosphate phosphatase.	6.44932e-106

>NZ_CP033687.1|WP_026684984.1|1601522_1602905_+|glycine--tRNA-ligase
MSVTMDQIVSHAKHRGFIFPGSEIYGGLANTWDYGPLGVEFKNNVKKAWWKKFIQESPYNVGLDAAILMNPRTWEASGHLGNFNDPMIDCKHCKARHRADKLIENALHEKGIDMIVDGLPFEKMEALIKEHDIACPDCGSKDWTGIRQFNLMFKTYQGVTEDSTNELYLRPETAQGIFVNFKNVQRTMRKKLPFGIAQIGKSFRNEITPGNFIFRTREFEQMELEFFCRPGEELKWFDYWKQYAREFLLNLGMREENLRLRDHEKEELSHYSNATTDFEYNFPFGWGELWGIASRTDYDLKRHMEYSGEDFTYLDQETNERFVPYCIEPSLGADRVALAFLIDSYAEEELEDGTSRTVMHLHPALAPYKAAVLPLSKKLSAEARDIFSDLSKTFMVDFDETGSIGKRYRRQDEIGTPFCITYDFDSRDDHMVTVRDRDTMEQTRVPITELKAFLEEKIKF
>NZ_CP033687.1|WP_061565278.1|1599992_1601015_+|HD-GYP-domain-containing-protein
MVFQKGEKLEEDLYSNSGVLLLRKGTFLTERLAAILNKYEVLRDPELDGRRIATEVPGIFHDLLYESIYHEMEELQRIIQVKTTLCDAEVESMEKNFRKLYKEVFTTRTSILELMEHFSADEYLFKHCIHVGLIAANIGKILKLDPEKQSLLAQMGLFHDIGKFTIDPQILNKPGRLTDEEFALIKKHPEAGYRLLEKTSLDPMILKGTLMHHERLDGSGYPDGRKTIPFLVRILSVADTFDAICSNRAYRRRQPVFFAIDELMADADAGRLDREIVLPFANFLMENYRKQPITLRNGVKGSIIRIHPLHPNQPVLKVEGYPVLNLMEQKLTLFQIANPY
>NZ_CP033687.1|WP_142010224.1|1598739_1599444_-|hypothetical-protein
MSISVFRRTSEYRLLFWCGFPVLESILSGQTSGFAWLLDIQFFQLPTALSVSENRPLPRNFRDKRASALLYLDSRIYFSFPVTLPVSEKDCSHAFSATNEYHLCFAWISVSISVFRRTSEYRLLFWCGFPVLESILSGQTSGFAWLLDIQFFQLPAALSVSENRPLPRNFRDKWASALLGFPYLFQLSSRTSCFGKRLLPSNFTQQMGIGFVWIPFLFQLSAALSCFRKWMTSA
>NZ_CP033687.1|WP_035182624.1|1598317_1598791_+|hypothetical-protein
MSDVLLLLQMVAKRLSILSLITAVLLLLSHLWLYAVFAFIIMGGLICVDRIISEKGNSRAAENRRYYTLIVVTDEDWYEEEHVPFLEMDHVSLELHYQYEDIRRINPLIQLQAFPGFVLVETDDTKRIEESLQNPALVTGNYAEVIHFLKQESAAES
>NZ_CP033687.1|WP_061087273.1|1597055_1598174_-|NADH-dependent-flavin-oxidoreductase
MSKYDKLFEPITFKSGVRAENRIVMAPMTHYSSNDDGTISDAELRYYAERAKGPGMVVTACANVTENGKAFTGQPGAHTDEMVESMKKLAQTIQQNGAKAVVQIHHGGRECPAELVPGGDVVSASETDSSDGSVHARALTGEETAEIVKAFGEATRRVIEAGFDGVEIHGANGYLIQQFFSPYTNWREDEWGGSLEKRLAFPLAVVDAVKKTVAEYADRPFLVGYRLSPEEPYEPGITMDDTFALLDALMEKELDYVHISLQHFWSKARRGGEPGRPRMEQIVEHVAGRVPLIGVGSLHTGDEVLKAMETDVPLIALGRELVMEPHWVEKIKAGQEDAIQTALRKDDRERLVIPEPLWKMIISTPGWFPFAE
>NZ_CP033687.1|WP_013858263.1|1595639_1596176_-|YceI-family-protein
MTKTKWAVDYAHSTIDFTVKHMMISKVKGSFQNFEAEIEADPQDLTDAKVSFIVDARSIHTKNDDRDNHLRSADFLDVEQYPNITFVSKSVTKAGDNDYNVTGDLTIHGVTKEETFKVTFEGISKNPMSGAETAGFSAEGTVKRSNYGLTWNAALETGGVLVGDEIKFTVELEASKAE
>NZ_CP033687.1|WP_035182628.1|1594582_1595287_-|iron-sulfur-cluster-repair-di-iron-protein
MERFTTSQTVGEIVTLFPKAADLFKANRIDFCCGGNVSVKEAAEKRNLSADELLDAICNLYGQYAGKGTEQNWNEAGYTEIVNYIQATHHAFLREELPNLSPYVTKVMRVHGGNHPHLIEVHELFNQLKAELLEHTEKEDTEQFPAIRAYENLPTAANLKAATAGLTDLETEHAAVGEILHRLREITNDYTLPEGACRTFQLVYHRLENFENDTFQHIHLENNILFKRLLEEAV
>NZ_CP033687.1|WP_014096278.1|1592975_1593656_+|Crp/Fnr-family-transcriptional-regulator
MENLRKMPLFKGLGDADLAVIADISVKKHAEKDAHIFFQGDPQEAVYFIESGEVKIYRTDANGKEQVVTLLRDGDMFPHVGFFRKISYPANAMAVVDTNLVAIRITDFENVLLNNPQLTMTLYGVMSDEILDLQDRLEAQILNNAYEQVVKLFLRLTRTHGVQEKDGFVLVKTPLNNSDLANMIGVTRETVSRTIRQLKEKNLILPQEKGTYLIHQEKLTEELLGV
>NZ_CP033687.1|WP_110133769.1|1591401_1592670_+|C4-dicarboxylate-transporter-DctA
MRINFRNLTVQVIIGIILGIIVGLVSPKFGAELNILAQWFIKLIKMLVPPIIFFTVIIGIGGMGDLKKVGRIGGKALIYFEVVSTVALAIGLIIVNLIQPGHGIDTSHAKTSQVSQFVTQAKDSEHGFIGFISGIIPESIAGAFVKGDLLPILFFAVLFGVAAASLGERAKPVIRFFEDMTEVFFEIVGIVMKVSPIAAFGAMAYTVGQFGASSLINLGELMGSVYLTMIIFILLVLGGIAKAFGFNIFKFIAYIKEELLLVLGTSSSESAMPSLMRKLEKFGCSKSVVGLVVPTGYSFNLDGTAIYLSMASIFIAQAYNVHLTIGHQIMLLLILMLTSKGAAGVTGSGFITLAATLSAFPVIPVAGIALLIGVDRFMSESRALTNIIGNAVATVVISKTEKEFDKNEALETAAHPTESIPS
>NZ_CP033687.1|WP_061087274.1|1589502_1591131_+|glycerol-3-phosphate-dehydrogenase/oxidase
MEFSGKERGAVLQNMKDKTFDLLVIGGGITGAGIALDAVSRGMSVALVEMQDFAAGTSSRSTKLVHGGLRYLKQFEVKMVAEVGKERAIVYENGPHVTTPEWMLLPFHKGGTFGAFTTNIGLRLYDFLAGVKKTERRKMLSASETLNKEPLIKKDGLKGGGYYVEYRTDDARLTIEVMKAAVAHGALAVNYTKAEEYLYENGRISGATVRDQISGETVNVRAKMVVNATGPWSDKMRNKDGKGSKSLRLTKGVHIVFDQSIFPLRQAVYFDTPDGRMVFAIPRGDKTYVGTTDTFYDKDPIHPKPLPKDIDYLLKAIHFMFPKVKVTARDVESSWAGVRPLIYEEGKDASEISRKDEIWESDSGLVTIAGGKLTGYRKMAETVVDLVARRLGGNFQPCQTKHLPISGGDVGGSENLPAFVKAKTKEGEASGLSAEASRAIAEKYGTNADHVYAYAKSWKDDYPLPREVYAVLKYAVEQEMVVKPVDFFIRRTGALFFDINWVRKWKEPVIAWMAAEFSWDEETEQAYRKELEEALREAVPEV
>NZ_CP033687.1|WP_110133771.1|1604087_1605908_+|APC-family-permease
MFTMIKRLLIGRPLRSNELEGQKLTKLKALAILSSDALSSVAYGPEQVLIVLATVGALAFWYSIPITVGILILLAALILSYRQVIYSYPQGGGAYLVSKENLGVTPGLLAGGSLLVDYILTVAVSVSAGTDAITSAFQSLHPYSVQIAVFLVLIITILNLRGLTESANVLAYPVYLFVFALIVIIVVGLFKTVTGQVPQNLHPHIGTPVAGISLFLLLKAFSSGCSALTGVEAISNAIPNFRDPAPRNAARTLAMMGIILASLLAGISFLAYWLGIAPKETETVVSQMAHRTLGNGVLYYFVQATTALILVLAANTGFSAFPQLAFNLARDKFMPRMFTIRGDRLGYSNGIIFLGVASMILIVAFQGNTERLIPLYAVGVFIPFTLAQCGMIVKWVTQRPRGWAGKMSVNFVGAIITFSVLAILFITKFTQVWPVLIFLPIVMFIFRKVNRHYEAVGEQLRIKGVFQEEIHSNVIIVPVAGITTVVERTINYAKSLSDQVIAVYVAFDHEDEKRMEEKWKEWDCGVRLVTLHSSYRSIVQPLAKFLEIIQRKAKENKYQVMVLIPQFIPKKRWQNILHNQSALLIRMRLLWEKDVVVATMPYHFKK
>NZ_CP033687.1|WP_013858270.1|1606072_1606909_-|undecaprenyl-diphosphate-phosphatase
MHLWNLFVAAILGLVEGLTEFAPVSSTGHMIIVDDLILKSNHLYGTEAANVFKVVIQLGSIMAMVVVFWDRFLNLLGLKKNITREQMYGERLRLTHVITGLVPAAVLGFLFEDYIDAHLFSVNTVLVALVVGAILMIVADLTRPRRPKTETVDQITYRQAFVVGLFQCLALWPGFSRSGSTISGGVLLGMSHRAAADFTFIMAVPIMFGASFLSLVKHWGAVTPETIPFFITGFISAFIFALIAIKFFLALINKVKLVPFAIYRILLAIVLLLLIWNR
>NZ_CP033687.1|WP_017551739.1|1607083_1607269_+|twin-arginine-translocase-TatA/TatE-family-subunit
MPGNLSFGEVLIILVVALLIFGPSKLPQLGRAAGQTLREFKKGVRDAIDEEEKPQVKKSKS
>NZ_CP033687.1|WP_014097040.1|1607910_1609326_+|ISLre2-like-element-ISBco6-family-transposase
MDIISIIAGLLKDTKSLIEFEEQLKLLMQKAFTQWVGEIFEELDKIIKQEKLEEGWVYCRSDNRNIQFLFGSVTFKRSLMHDKRGNSHYPLDEWLGLVPHQRYSPLVELKVAELASENTYREVADILKEWTAVSLSHTTVGNMVKHVGKTQAEADKALVEELEIAVSLPEGKKVDYLFSEADGVFVRGLKKKQSMEVHHAILYEGWQTNGKRVSLRQPTVIMTTEAIQTFWDEVQATAANTYSLEKTHVITNSDGGAGYTAERFQTAFSQSEFPVLNQLDTYHVAQAIIRTFGGGKSEIKEQIRKAIRTHDLDQLTLYLDTHESTLTDKKALKKIKEFRSYILKNWDRIFDWRDRVKNVPEGARGLGAMESNQRHISFRMKKRGMHWSELGAEAMVKIKQGILNGTLREVYLKHRSRSERKQRNLKQFIRMSQLLKQPVRPSVGVKHGSVALHSSSSSAMGHLSKILELSF
>NZ_CP033687.1|WP_110133772.1|1609722_1610748_+|AI-2E-family-transporter
MEDRLFSLFQKRGVRRVLIFVLLTLILYFLRSMMDLMLLTFIFSYLVNRLQKIVTRWFPIKRRLAVLIVYILILGGLTFGVIKYFPILVNEITQLVVQISDFYTKPQHNEVLNYIVKNIQEKKIVDYAQKGVSILLDYFTSISKVSIQVFMAIILSLFFLLEKERIIRFTKQFKTSKLAAFYDEIEYFGVKFVGTFGKVIEAQFIIAVVNSVLTTIGLWILGFPQLFGLAILIFALGLIPVAGVFISLIPLCIIAYSIGGGMKVLYVLILIVIVHAVEAYVLNPQLMSSKTNMPVFYTFLILIFCEHFFGLWGLILGIPIVMFFLDVLEVTGRSTEPKKKT
>NZ_CP033687.1|WP_026684940.1|1611088_1611817_+|amino-acid-ABC-transporter-ATP-binding-protein
MISFRHVNKYYGDFHVLKDINLEVKEGEVVVVIGPSGSGKSTMLRCINRLEDITDGELFVRNMKVNDKKTDINDLRKNIGMVFQHFNLYPHRTVLQNITLAPIKVLGQSKEEAEKKAMHYLERVGIPDKANAYPSQLSGGQQQRVAIARGLAMEPDIMLFDEPTSALDPEMIGEVLDVMKALAKDGMTMVVVTHEMGFAREVADRVLFMDQGRIIEDNTPEDFFKNPREERARTFLNRVLNH
>NZ_CP033687.1|WP_014096261.1|1612381_1613197_+|transporter-substrate-binding-domain-containing-protein
MGKVKKWLAAGLVFILAAALVAGCGKSKSTGGSGSASDDPIKKIEDRGKLVVGVKYDTYLFGYKDPKTGNVEGFDVDIAKAISKKIFGDKVKVELKEVTSKTRIPMLQNGDVDMVVATMTISPDRKKVVDFSDVYFDAGQSLLVKKGSKIKSVKDLTKGTKVLTVKGATSGDNVRKAAPDTTVLEYENYQEAFTALKSGKGDALTTDNSILYGMAAQDSNYQVVGGTFTKEPYGIAMKKGNTKLVKAVNKALKELKDSGEYDKIKNKWIKE
>NZ_CP033687.1|WP_014096260.1|1613262_1613916_+|amino-acid-ABC-transporter-permease
MLDFSILTDNIDLYMKGFVNTIKISIIGLVASFILGNLIAVFRLAPVKLLNFIGAVYVEVIRNIPLILTGFFFYNGLSYFHINLSGFIAGTIALSIYTAAFIAEAVRAGIQSVDKGQLEAARSTGLTYTQAMRYVVLPQAIKIVIPPIGNQFLNLVKNSSILGVFAGLDLMYYADLIHEKTWITFDTYIFVGMFYLILTIPLSLLVNYLERRLARSS
>NZ_CP033687.1|WP_014096259.1|1613941_1614649_+|amino-acid-ABC-transporter-permease
MDFAGAYSSGNLAYLLKGFAVTLEVAFVAIVLSFLIGCILGILRYAKIPILSPIVALVVEITRNLPLILIIFFTYFALPEVGMKMSVTAAAISALTVFESAMIAEIVRGGLNAIPKGQIEAARSSGLKYIQTLWYIILPQALKKMIPPLVSQFISLLKDTSLAIIIALPELLHNAKGIYNGEGGSKYIIPILLMAAFMYFVVNYLLSILARRLEKRLDPDRSAAKQLVNTTENLL
>NZ_CP033687.1|WP_017551743.1|1614823_1615225_+|GntR-family-transcriptional-regulator
MLMKIDLESNVPIYQQLHNSIIEGIASKELAPGDSLPSVRAMASDLGVNMHTVNKAYQILKQEGFIQIHRQKGVVIQPEQMPPADEPYLESLTGKLRPLISEAICRGLDEKQFLKICEKLYNDIQKVGEQWKP

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Crispr_ID: NZ_CP033687_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_8

1775201-1775292

Orphan

Consensus_repeat	Method
TTCCTTTTCTGGTGTGGGCCGTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_8

>merge|NZ_CP033687|8|1775201-1775292|CRISPRCasFinder
TTCCTTTTCTGGTGTGGGCCGTTTTTTGTCGTTTTTGAGTCATATAGCGGCCGACCTTGCCCCGCAGCCTTCCTTTTCTGGTGTGGGCCGTA

>NZ_CP033687|8|7|1775201-1775292|CRISPRCasFinder
TTCCTTTTCTGGTGTGGGCCGTT	TTTTGTCGTTTTTGAGTCATATAGCGGCCGACCTTGCCCCGCAGCC
TTCCTTTTCTGGTGTGGGCCGTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_110133821.1\|1773640_1775050_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP033687.1\|WP_035191172.1\|1771044_1771860_+\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|379207
NZ_CP033687.1\|WP_110133822.1\|1781432_1782812_-\|sugar-porter-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340917
NZ_CP033687.1\|WP_014096119.1\|1780062_1781145_-\|iron-containing-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|341451
NZ_CP033687.1\|WP_110133820.1\|1770168_1770741_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380348
NZ_CP033687.1\|WP_110133823.1\|1782801_1784337_-\|xylulokinase	unknown	unknown	gnl\|CDD\|198374
NZ_CP033687.1\|WP_014096115.1\|1785939_1787112_+\|ROK-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366120
NZ_CP033687.1\|WP_110133825.1\|1788353_1789205_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	unknown	unknown	gnl\|CDD\|181221
NZ_CP033687.1\|WP_014096121.1\|1777070_1778648_+\|YifB-family-Mg-chelatase-like-AAA-ATPase	unknown	unknown	gnl\|CDD\|223679
NZ_CP033687.1\|WP_110133743.1\|1766003_1767398_-\|transposase	unknown	unknown	gnl\|CDD\|379252
NZ_CP033687.1\|WP_061566168.1\|1784396_1785731_-\|xylose-isomerase	unknown	unknown	gnl\|CDD\|235487
NZ_CP033687.1\|WP_110134284.1\|1764819_1765857_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|235935
NZ_CP033687.1\|WP_014096120.1\|1778592_1779567_+\|transposase	unknown	unknown	gnl\|CDD\|227751
NZ_CP033687.1\|WP_061577833.1\|1767569_1768598_+\|IS1595-family-transposase	unknown	unknown	gnl\|CDD\|226202
NZ_CP033687.1\|WP_035182475.1\|1772483_1773200_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293807
NZ_CP033687.1\|WP_013858390.1\|1769724_1770018_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_110133824.1\|1787259_1788357_-\|quinolinate-synthase-NadA	unknown	unknown	gnl\|CDD\|236489
NZ_CP033687.1\|WP_017551900.1\|1763985_1764546_+\|maltose-O-acetyltransferase	unknown	unknown	gnl\|CDD\|100047
NZ_CP033687.1\|WP_110133826.1\|1789173_1790766_-\|L-aspartate-oxidase	unknown	unknown	gnl\|CDD\|236147
NZ_CP033687.1\|WP_061577834.1\|1768654_1769224_+\|dihydrofolate-reductase	unknown	unknown	gnl\|CDD\|223340

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_110133821.1\|1773640_1775050_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	6.10677e-167
NZ_CP033687.1\|WP_035191172.1\|1771044_1771860_+\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|379207	pfam13472, Lipase_GDSL_2, GDSL-like Lipase/Acylhydrolase family. This family of presumed lipases and related enzymes are similar to pfam00657.	4.28273e-19
NZ_CP033687.1\|WP_110133822.1\|1781432_1782812_-\|sugar-porter-family-MFS-transporter	gnl\|CDD\|340917	cd17359, MFS_XylE_like, D-xylose-proton symporter and similar transporters of the Major Facilitator Superfamily. This subfamily includes bacterial transporters such as D-xylose-proton symporter (XylE or XylT), arabinose-proton symporter (AraE), galactose-proton symporter (GalP), major myo-inositol transporter IolT, glucose transport protein, putative metabolite transport proteins YfiG, YncC, and YwtG, and similar proteins. The symporters XylE, AraE, and GalP facilitate the uptake of D-xylose, arabinose, and galactose, respectively, across the boundary membrane with the concomitant transport of protons into the cell. IolT is involved in polyol metabolism and myo-inositol degradation into acetyl-CoA. The XylE-like subfamily belongs to the Glucose transporter -like (GLUT-like) family of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.72089e-167
NZ_CP033687.1\|WP_014096119.1\|1780062_1781145_-\|iron-containing-alcohol-dehydrogenase-family-protein	gnl\|CDD\|341451	cd08172, GlyDH-like, Glycerol_dehydrogenase-like. This family contains glycerol dehydrogenase (GlyDH)-like proteins that have yet to be characterized, but show sequence homology with glycerol dehydrogenase. Glycerol dehydrogenases (GlyDH) is a key enzyme in the glycerol dissimilation pathway. In anaerobic conditions, many microorganisms utilize glycerol as a source of carbon through coupled oxidative and reductive pathways. One of the pathways involves the oxidation of glycerol to dihydroxyacetone with the reduction of NAD+ to NADH catalyzed by glycerol dehydrogenases. Dihydroxyacetone is then phosphorylated by dihydroxyacetone kinase and enters the glycolytic pathway for further degradation. The activity of GlyDH is zinc-dependent; the zinc ion plays a role in stabilizing an alkoxide intermediate at the active site.	0
NZ_CP033687.1\|WP_014096120.1\|1778592_1779567_+\|transposase	gnl\|CDD\|227751	COG5464, COG5464, Uncharacterized conserved protein [Function unknown].	5.53097e-09
NZ_CP033687.1\|WP_110133823.1\|1782801_1784337_-\|xylulokinase	gnl\|CDD\|198374	cd07808, FGGY_D-XK_EcXK-like, Escherichia coli xylulokinase-like D-xylulose kinases; a subgroup of the FGGY family of carbohydrate kinases. This subgroup is predominantly composed of bacterial D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17), which catalyze the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. D-xylulose has been used as a source of carbon and energy by a variety of microorganisms. Some uncharacterized sequences are also included in this subgroup. The prototypical member of this CD is Escherichia coli xylulokinase (EcXK), which exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of Mg2+ or Mn2+ is required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	0
NZ_CP033687.1\|WP_014096115.1\|1785939_1787112_+\|ROK-family-transcriptional-regulator	gnl\|CDD\|366120	pfam00480, ROK, ROK family.	3.349e-71
NZ_CP033687.1\|WP_110133825.1\|1788353_1789205_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	gnl\|CDD\|181221	PRK08072, PRK08072, carboxylating nicotinate-nucleotide diphosphorylase.	2.09329e-158
NZ_CP033687.1\|WP_014096121.1\|1777070_1778648_+\|YifB-family-Mg-chelatase-like-AAA-ATPase	gnl\|CDD\|223679	COG0606, COG0606, Predicted ATPase with chaperone activity [Posttranslational modification, protein turnover, chaperones].	1.16274e-166
NZ_CP033687.1\|WP_110133743.1\|1766003_1767398_-\|transposase	gnl\|CDD\|379252	pfam13546, DDE_5, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	5.51168e-05
NZ_CP033687.1\|WP_061566168.1\|1784396_1785731_-\|xylose-isomerase	gnl\|CDD\|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_CP033687.1\|WP_110134284.1\|1764819_1765857_-\|SDR-family-oxidoreductase	gnl\|CDD\|235935	PRK07109, PRK07109, short chain dehydrogenase; Provisional.	4.73891e-145
NZ_CP033687.1\|WP_061577833.1\|1767569_1768598_+\|IS1595-family-transposase	gnl\|CDD\|226202	COG3677, COG3677, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	9.30653e-16
NZ_CP033687.1\|WP_035182475.1\|1772483_1773200_+\|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.	1.34643e-74
NZ_CP033687.1\|WP_110133824.1\|1787259_1788357_-\|quinolinate-synthase-NadA	gnl\|CDD\|236489	PRK09375, PRK09375, quinolinate synthase NadA.	2.70387e-154
NZ_CP033687.1\|WP_017551900.1\|1763985_1764546_+\|maltose-O-acetyltransferase	gnl\|CDD\|100047	cd03357, LbH_MAT_GAT, Maltose O-acetyltransferase (MAT) and Galactoside O-acetyltransferase (GAT): MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively at the C6 position of the nonreducing end glucosyl moiety. GAT specifically acetylates galactopyranosides. Furthermore, MAT shows higher affinity toward artificial substrates containing an alkyl or hydrophobic chain as well as a glucosyl unit. Active MAT and GAT are homotrimers, with each subunit consisting of an N-terminal alpha-helical region and a C-terminal left-handed parallel alpha-helix (LbH) subdomain with 6 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X).	4.19244e-105
NZ_CP033687.1\|WP_110133820.1\|1770168_1770741_-\|cupin-domain-containing-protein	gnl\|CDD\|380348	cd02219, cupin_YjlB-like, Bacillus subtilis YjlB and related proteins, cupin domain. This family includes bacterial and fungal proteins homologous to YjlB, a Bacillus subtilis protein of unknown function with a cupin beta barrel fold. The active site of members of the cupin superfamily is generally located at the center of a conserved barrel and usually includes a metal ion. The different functional classes in this superfamily include single domain bacterial isomerases and epimerases involved in the modification of cell wall carbohydrates, two-domain bicupins such as the desiccation-tolerant seed storage globulins, and multidomain nuclear transcription factors involved in legume root nodulation.	4.68884e-74
NZ_CP033687.1\|WP_110133826.1\|1789173_1790766_-\|L-aspartate-oxidase	gnl\|CDD\|236147	PRK08071, PRK08071, L-aspartate oxidase; Provisional.	0
NZ_CP033687.1\|WP_061577834.1\|1768654_1769224_+\|dihydrofolate-reductase	gnl\|CDD\|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	9.26775e-38

>NZ_CP033687.1|WP_110133821.1|1773640_1775050_+|group-II-intron-reverse-transcriptase/maturase
MKVTEETNKCRKQEETCCQKDTAEQEGYDRGHSFKRITENNTTNTNRQNEWMLERILSSNNLHRAYKKVKKNKGAGGVDGMKTGELLAYLTEHQRELVLSIRNGTYKPQPVRRVEIPKDNGKTRKLGIPTVVDRVIQQAISQVLVPIYERKFSDNSYGFRPHRSTNQALLKCQKNVNEGYQYVVDLDLEQYFDTVNHSKLIQILSETIHDGRVISLIHKFLNAGVMIKGIRTTNDFGVPQGGPLSPLLANVMLNELDKEMEARNHRFVRYADDVIIFCKSRRSCERTYHNILPFIERKLRLKVNREKTMITHIRNIKFLSYGFYLYEGKCKFRVHPKGVQKLKEKIRRITGRSNGLSVEERKKGLNDTVRGWVNYYKLADMKSLVTRLDQWTRRRMRMVTWKRWKRVRTRFYWLKKLGINKRKAWEWANTRKGYWRISGSHILARTLTNELFRRARYISFLDYYLSVRS
>NZ_CP033687.1|WP_035182475.1|1772483_1773200_+|MBL-fold-metallo-hydrolase
MKKIAEGVAMLEINLNHFIIHPTLIWDEQKAVLVDAGMPGSLDLIHAEMEKAGVPFEKLDAVILTHQDMDHIGSVPEILAESGHSITVYAHGLDKPYIEGERLLIKADPEKIDPARWESMPEEMKQMYLNPPKAKVDKVIGDGEVLPFGGGIEVIFTPGHTPGHCCLYLKKSKTLIAADAMVADNGKLHGPRQQVTPDMGTAMASLKKLLDFDIESVICYHGGLCHENVNEQIRKLAE
>NZ_CP033687.1|WP_035191172.1|1771044_1771860_+|SGNH/GDSL-hydrolase-family-protein
MGKKGWLVVLLFFITAGVLGTGNWYYQANTGKTIEKAQQQYKKDLAKEKKRSLEAKAAKESAAKQIYEKHKGKELVYLPVGSSLTAGDFATKKSKTYAALLAARIHQGLGYKVKTINGYGKSGAGLKEHGADSLPHIIFNHPDLVTIEFGTFDLNRNAKNTYVSAGQFKKDLEHFVDEIRKSTGKKTKIILLTTWNSGQLSFTYDRAIEEVGKAKGVPVANIESVWLNRSDTHGQKGEKAATGKSDGWLANDKGHKEIANTVYKKAYGLLK
>NZ_CP033687.1|WP_110133820.1|1770168_1770741_-|cupin-domain-containing-protein
MKRLLPFMSASDGKDAGGTAANDNVSAFYFEENGGIPNNPFLPVLIYHGVFKGRTDEIEKVFQKNNWGNNWVWTIFPYHHFHSNSHEVNAVRSGHAKVQLGGPQGKIFTISEGDCVLLPAGTGHKRIESGGGFAVTGGYPGGQDYDTQMRADETLRENIRKTGMPETDPVFGKNGPLFSYWTPEPGGKAG
>NZ_CP033687.1|WP_013858390.1|1769724_1770018_-|hypothetical-protein
MKEILEQVKEKLENAYNHPDSADLDACIRQLQDARQQYGDKGTMIEDAITAIEQAKHSIPEHRHAGTDSAAGAFGQAYNALEHAIESFSGTENNDPF
>NZ_CP033687.1|WP_061577834.1|1768654_1769224_+|dihydrofolate-reductase
MTNNVKQRKIILDLAVTLDGFIEGKNGEVDWCIMDPDMGFTDFLNQIDTILYGRKSYDLWGQYIPKNEDPDIEKEIWKLVHSKKKYVFSRTQNKIDNQAIFINDNILEEVNKLKKKSGKDIWLYGGASLITTFINLGLVDEFRLSIHPVVLGEGKPLFIDLKQRINLKMVNTRTFSSGVVQIIYHWNGN
>NZ_CP033687.1|WP_061577833.1|1767569_1768598_+|IS1595-family-transposase
MSKAFSNLLKYIDKLPHTQKEQVYQWVKRYVEPSSSAGGRLINEMRETRFKDGFECPHCSSEHVVRFGKYNGRQRYHCKCCGKTFTDTTNTVLYRTRKGNEWITFVDCMFKGYSLRKSAEIVGVTWVTLFYWRHKLLNALKQMDFEHFDGIVEIDETYFLYSQKGQRGITERKPRKRGGKSKHRGISHEQVCVLVARDRTKATVSKVACMGRIVKSKVDTLIGSKLSNENVLVTDAWRAYKTYAKEKGLEHFRIKSDSGKHVIKGLYHIQNVNGLHSRLKQWIDRFKGVATKYLDNYLAWFLFVDSRSNESTKQHIKEFLLTSYVFEMKDTYNSLRLSKFVV
>NZ_CP033687.1|WP_110133743.1|1766003_1767398_-|transposase
MATILPDLNQKENIYSETTRFFKQAKLGVFLHRSNIHKVKGVSALSIIRFVFSLVLHGMSFSRALKSDHIPKDFRKDVVYDLLKNPTYNWRKLLVLVSTYLIEKFIRPLTSERRDCVLIFDDSAFYRNRSKCVELLARAKDHAHHVYFKGFRMLTLGWSDGATFLPLAFSHLSSPKAKNRFQEMDSSIDKRTVGYKPRKEAIQKTTETMFNLLNAVDPEKLGAKAVLFDSWFAFPSTIAKIVRNYSLDVVCMLKDLPRVSYHYEGQSYRLSQLYKMVRKKRGRAKILASIVVGLGHNDEYGQEIQARIVFVRDRNRSKKWLALLTTNMNHTDEDVVRIYGKRWDIECFFKVTKSYLKLGKEFQCQSYDSMFAHTTIVFLRYLMLSLRAREEEDPRTLGQLFYMYCEEIDDIQFAEALLTIIEALGQTLAESFLLTDEKIQDFLDCFINKLPSFLQKPLLKSEAA
>NZ_CP033687.1|WP_110134284.1|1764819_1765857_-|SDR-family-oxidoreductase
MDASMEKPLSLKKLADQVIVITGASSGIGLATARMAAARGARLVLAARNEHALKILVNELKDNGGSAVWVQADVGREEDVKHIAATAIKTFGGFDTWVNNAGVSIFGEAMDVSIEDMKRMYDTNFWGAVYGTRLAVHHYKSRGVPGAVINIGSLFGDRGTVIQSTYASSKFALHGFTESIRMELEKEHAPVSITLVHPGRIDTPYNEHARSYLKKQPAHYMSMIYPPQAVAEAILFAAEHPKRDMYVGSQAKMVAVLGRFLPRFMDKLMELTMYRTQHSDRPSKSKADSALYHPGYGLHERGTNKGWMRRNSYYVKMSKYPLASAAIAAFVGAALWAAVSPRQKD
>NZ_CP033687.1|WP_017551900.1|1763985_1764546_+|maltose-O-acetyltransferase
MSTEKEKMIAGKLYNAGDPELAQARLKARRLVRTFNETDETDLETRTALLKKLFGSTGERLFIESDFRCDYGFNIHVGENFYANFDCVILDGGPVEIGKNCMLAPGVHIYTATHPLDAKTRVSGLELTKPVKIGDNVWIGGRAVINPGVTIGNNAVIASGAVVVKDVPDNAVVGGNPARIIKMAES
>NZ_CP033687.1|WP_014096121.1|1777070_1778648_+|YifB-family-Mg-chelatase-like-AAA-ATPase
MATIISSIGLKGIEGYCVHAEVQMMLGCGSGITIVGLPDASVKESKERIRGACSSIGCMLFQSKTIVNLSPADERKNSPALDLPIAIGLMAENHFFHARIPDHTAFLGALSLDGSVQAVAGMLPYVMAARGLGMKRLYLPASAELPFSQMDGMDIIFVQHLKDVLDSLSGKKLPPVRKKRQLQPDEYSFEADFSMILGHRHAKKVLEIAAAGSHNVLMYGPPGSGKSMLAEAFPSILPPLSETSSFEVAGLYQLANVKRGFHRKPPFRAPHHASSAVSLVGGGSRPHPGEISLAHHGVLFLDEMAEFPKRTLDMLRQPLENGKVTISRAASTVTYPARFIMLAAMNLCPCGYLGSPHAYCTCTPKQIQAYQNRISGPLLDRFDIFLPVGTVPLLEESGKINETSEQIRTRVTEARKRQYERYGAEVCNGTVPNEIFLQKNPLANSSSLMLRQWASKENFSSRAQMKILRLARTISDLQGSRELSEDALWQALQMKRNHLFGKRKVDAYATYNGRKSGVFAARPLV
>NZ_CP033687.1|WP_014096120.1|1778592_1779567_+|transposase
MQLIMEEKAEYLPHDRLFKELIQTFFADFMEAFFPEVARWMDFSDVEFLQQDLFTDITAGEQRRIDILAKLKLKGEDTVVLIHVEPQSYYQMEFPERMFIYYSRIYEKYRLPVLPIAVFSYNKRRETPSLFTVRIRNFESIRFRYMSIHLIRKNWKEYIRSNNPVAAALLSKMGYTKKEKVQVKVEFLRMMARMELDPARMALIYGFFDSYFKLTDKEDELVMSSIKNLDPQEADQILRLPNSFYDKGYKKGKEEGKEEGKEEGKEEGLKEGLKEGERRAALRIAKRMLEENQDLASIAKYTGLAEEELKKLKQSGATRLRCDQ
>NZ_CP033687.1|WP_014096119.1|1780062_1781145_-|iron-containing-alcohol-dehydrogenase-family-protein
MRLSQVIRSGPNQYICEEEAAKYLEEKLEEFRHPVVITGVKSFEAFQEFASVPQNWPVLQYDHTASEKNMAELAEQAGRADVIVGIGGGKVLDTAKGTAELLNCEVVLVPTLAGTCAGYTPLSAVYHEDGSFSHVAYYKRSAFLTLIDLRILLNAPAEYLLGGIGDSLAKWYEAEGITRSMKHLPVMVELGLRSAKAIYEGILRDSEQALHDRNEGKITDAFRNIVEIIIGAAGTVGGFAGEYGRMAGAHAIHNGLSFLPETHSILHGSKVAYGILVQLAATGDINEVKKLLPLYQKLGFPYNLDTLHVTENHGAAIEKVAAYAAKPEESFRLLGSFTKAQIAKAMETIEQLTAEKADIK
>NZ_CP033687.1|WP_110133822.1|1781432_1782812_-|sugar-porter-family-MFS-transporter
MKFKINNGLIYFFGALGGLLFGYDTGVISGALLFIKNDLHLTSWTEGIVVSSILFGCMIGAAISGAMSDRWGRKKVVLIAASVFCIGALGTALAPNTGVLILFRVILGLAVGSASTLVPMYLSEMAPTSIRGALSSLNQLMIMTGILLAYIINYVFAATGSWRWMLGFALIPGLLMLIGMLFLPESPRWLLKQGKEPEARTILNYMRKGHGVEEEIREIKQANELEKNQGGFSEVKQAWVRPALIAGIGLAIFQQIIGCNTVLYYAPTTFTNVGLGASAAILGTVGIGIVNVIITAIAVLIIDKVGRKPLLLIGNAGMSLALFVLGIVNALLGPSTAASWTTVICLAVYIAFFSLSWGPVVWVMLSEIFPLKIRGIGMGIGSVTNWLANLIVSLTFPKLIEQFGISTMFIIYGIMGVLAFIFVTRKVSETKGKSLEQIEIDLRQQAEHKKFNFSQSIQK
>NZ_CP033687.1|WP_110133823.1|1782801_1784337_-|xylulokinase
MKYAIGVDLGTSSVKVLLVDQNGQVVSSVSKSYPLMQPHPGYSEQDPEQWVEKTVQALKELTEKSEVSRDEIEGLSFSGQMHGLVLLDENLQVIRNAILWNDTRTTEQCKKIDQVLGGKLLEITKNPALEGFTLPKMLWIQQYEPENFRKTRVFLLPKDYLRYRLTGTIGMDYSDAAGTLLLDIVNQSWSTDILRTFDIPAGICPPLVETEAEVGTLLPDIAATCGLSHATKVFAGGADNACGAIGAGILEEGKALCSIGTSGVFLSYESDSNKNFGGKVHLFNHGQKDAYYTMGVTLAAGYSLSWFKDTFAKGEDFATLLEEAAHSSIGANGLLFTPFIAGERTPYADAKIRGTFTGIDSSHTRRDFTRAVMEGIAFSINESVEIFRNYGKNIDTVVSIGGGAKSDLWLQIQADIFQAKVIKLQNEQGPGMGAAMIAASGLGWFSSLKDCAAAFIRTDRTFEPVPKNVKRYRDFYQVYKDVYPHTVAINHQLFDLRRVNESRFGGKTDEI
>NZ_CP033687.1|WP_061566168.1|1784396_1785731_-|xylose-isomerase
MAYFPNVSKITYSGKQLKSGLSFNHYNPKELVGGKTMEEQLRFSVAFWHTFTESGTDPFGAGSKIRPWDRFTGMDLAKARVEAAFEFFEKLGNPYFCFHDRDIAPEGDTLRETNKNLDVIVAMIKDYMKTSKVKLLWNTANMFTNPRFVHGAASSCNADVFAYAAAQVKKGLEVGKELGAENYVFWGGREGYETLLNTDLKLEQDNLARFFHMAVDYAKEIGFDAQFLLEPKPKEPTKHQYDFDAATTIAFLKTYDLDQHFKLNLEANHATLAGHTFEHEIRVARTHGLLGSLDANQGDPLLGWDTDEFPTDLYSTTLAMYEVLKNGGLGRGGLNFDAKTRRASFTDEDLFYAHIAGMDSFALGLKVANRLIEDRVFDAFIEERYSSYKEGIGADIISGKANFKSLENYIIDKKEITNQSGRLEQLKNTLNHYIVQEAYQSVNA
>NZ_CP033687.1|WP_014096115.1|1785939_1787112_+|ROK-family-transcriptional-regulator
MHIADQSFIKNQNQRVILNELMKHEQISRAKLAKITKLNKATISSQVSFLIEKKLVKEVGTGLSSGGRKPVMLVFNEKAGYAIGVDIGVTYILTVLTDLDGNMIYSDYCEIEDPSFEMIKPVIIERIRLVASKVSSSPYGIIGIGAGVHGFVDMQQNVLFTPNSGWRDVDLKGLLQTHFDCPVLVDNEANAGAYGEKLFGILKGCKNGIYVSIGIGIGLGIIVNDELYRGKEGFSGEMGHMSIDFNGRQCGCGNKGCWELYASEKAFYDQLCLVKNKRRITLEEVTNWVKENDGETLRELDKLGYFLGIGLTNIINTFNPEAIVLRSNLIQENPTILNSIQSTIASRVSKYVRQNHRIYLSQLHRNATAVGAAAFIVHHFLMESEELYGN
>NZ_CP033687.1|WP_110133824.1|1787259_1788357_-|quinolinate-synthase-NadA
MSLLKTLQLTALPEKYQSLAQEEMENRVWDIKKEMGAKLFLPCHHYQREEVYQFADAAGDSLQLAQISAKNRNAKYIVFCGVHFMAETADILTSAEQTVILPDMRAGCSMADMADIHQTERAWDMLQSLFGDTMLPLTYVNSTAAIKAFVGRNGGATVTSSNAKKMVKWAFTQKKRVFFLPDQHLGRNTAFDLGVELADMAVWDPIRNELIYEGALENVKVILWKGHCSVHAHFTIKNIEFVRAKYPDMQIIVHPECAHEVVALSDFSGSTKYIIDTIENAPAGSAWAIGTEMNLVQRLIKNHPDKKIISLNPVMCPCLTMNRIDLPHLLWSLENIIEGKETNVIKVEENTARDAVLALERMLKL
>NZ_CP033687.1|WP_110133825.1|1788353_1789205_-|carboxylating-nicotinate-nucleotide-diphosphorylase
MNKLKLQSMLKDFFMEDIGEGDINTEYIFSPDQPGKLTFIAKQNGIFCGKDVIEEGFRILDSTVRPRIFPRDGAWIEKGTVIAEIHGPIVSLLSGERVILNLVQRMSGIATTTNAAVRETKGTHAKICDTRKTTPGLRMLEKYAVKAGGGFNHRRGLYDCVMLKDNHIAFAGSITKAVETVKASIGHTVKIEVEIETKDHLLEAVRAGADIIMFDNRTPEEVCEWLPLVPPHIATEASGGITMENIRSYAETGVDWISLGFLTHSYQILDISAIVENTKEVAL
>NZ_CP033687.1|WP_110133826.1|1789173_1790766_-|L-aspartate-oxidase
MKEKICILGSGIAALQLAVHLDSRYDVTIITKSQTKTSNSYKAQGGIAAVLSPEDRFEFHVKDTIRAGCRHHNEKEVEKLVKEGAAVVEELVKSGLPADRRPDGGLDLGLEGAHTVHRILHCGGDATGKFVIQHLLGQLGKSVRIIEHELAFELMVSAETGRVTGVKTKTANGNIRHYFSDHTVIATGGLGSLYPFTSNHPEIIGDGIAMAYRAGAELADMEFVQFHPTLLYAEGRAKGLVSEAVRGEGAVLVDENGSPVMAGVHPLKDLAPRHVVAHQIHQTIHSGKKVFLDIRKIKHFEKRFPTISRICRESGIDIHSGLLPVVPGSHFFMGGIVVDTYGRTTVNGLYAIGEAAASGVHGANRLASNSLLEGLVFGKRLAAFLNALEPEASGGETAEIARPPLNPEIARRLDTAALKEKMMENAGVIRTETGLRHLLRWLEARGADTFSAFSLDHLTKEEIEKVFMFTNSFFITQSALFRKESRGAHIRADYPDESSDWQGIHLIHAKNKGLIARRGLYEQAQTSIHA

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Crispr_ID: NZ_CP033687_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_9

1949900-1949991

Orphan

Consensus_repeat	Method
GTTCTAGCCCTTGCAAAACCTTTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_9

>merge|NZ_CP033687|9|1949900-1949991|CRISPRCasFinder
GTTCTAGCCCTTGCAAAACCTTTGGACAAAGTTGTAAATAGTTCTACGCTGCCAATCTCATTTCTAAGTTCTAGCCCTTGCAAAGCCTTTGG

>NZ_CP033687|9|8|1949900-1949991|CRISPRCasFinder
GTTCTAGCCCTTGCAAAACCTTTGG	ACAAAGTTGTAAATAGTTCTACGCTGCCAATCTCATTTCTAA
GTTCTAGCCCTTGCAAAGCCTTTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_104851256.1\|1962108_1964211_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|180751
NZ_CP033687.1\|WP_014095967.1\|1958179_1959139_+\|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380509
NZ_CP033687.1\|WP_110133850.1\|1950893_1952045_-\|radical-SAM/CxCxxxxC-motif-protein-YfkAB	unknown	unknown	gnl\|CDD\|275271
NZ_CP033687.1\|WP_035182334.1\|1944781_1945702_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|235853
NZ_CP033687.1\|WP_014095964.1\|1960930_1961116_-\|Fur-regulated-basic-protein-FbpA	unknown	unknown	gnl\|CDD\|315692
NZ_CP033687.1\|WP_110133851.1\|1952345_1954865_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP033687.1\|WP_035182336.1\|1943056_1944715_+\|isovaleryl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173843
NZ_CP033687.1\|WP_035182338.1\|1941549_1943073_+\|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl\|CDD\|235730
NZ_CP033687.1\|WP_035182332.1\|1946148_1946976_-\|AAC(3)-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|376807
NZ_CP033687.1\|WP_110133849.1\|1950146_1950743_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014095973.1\|1949543_1949750_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_110133848.1\|1938554_1939298_+\|type-I-methionyl-aminopeptidase	unknown	unknown	gnl\|CDD\|237252
NZ_CP033687.1\|WP_014095974.1\|1948917_1949343_-\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP033687.1\|WP_014095963.1\|1961158_1961923_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|224561
NZ_CP033687.1\|WP_035182331.1\|1947082_1948411_+\|polysaccharide-biosynthesis-protein	unknown	unknown	gnl\|CDD\|240529
NZ_CP033687.1\|WP_014095965.1\|1959842_1960622_+\|Cof-type-HAD-IIB-family-hydrolase	unknown	unknown	gnl\|CDD\|319819
NZ_CP033687.1\|WP_035182340.1\|1941166_1941553_+\|MerR-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133403
NZ_CP033687.1\|WP_061087166.1\|1939519_1940101_-\|biotin-transporter-BioY	unknown	unknown	gnl\|CDD\|376871
NZ_CP033687.1\|WP_035182323.1\|1955089_1956151_+\|NAD(P)-dependent-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|176188
NZ_CP033687.1\|WP_014095966.1\|1959271_1959814_+\|SIS-domain-containing-protein	unknown	unknown	gnl\|CDD\|240138

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_104851256.1\|1962108_1964211_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|180751	PRK06922, PRK06922, class I SAM-dependent methyltransferase.	0
NZ_CP033687.1\|WP_014095967.1\|1958179_1959139_+\|LacI-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|380509	cd06286, PBP1_CcpB-like, ligand-binding domain of a novel transcription factor implicated in catabolite repression in Bacillus and Clostridium species. This group includes the ligand-binding domain of a novel transcription factor implicated in catabolite repression in Bacillus and Clostridium species. Catabolite control protein B (CcpB) is 30% identical in sequence to CcpA which functions as the major transcriptional regulator of carbon catabolite repression/regulation (CCR), a process in which enzymes necessary for the metabolism of alternative sugars are inhibited in the presence of glucose. Like CcpA, the DNA-binding protein CcpB exerts its catabolite-repressing effect by a mechanism dependent on the presence of HPr(Ser-P), the small phosphocarrier proteins of the phosphoenolpyruvate-sugar phosphotransferase system, but with a less significant degree.	2.26256e-117
NZ_CP033687.1\|WP_110133850.1\|1950893_1952045_-\|radical-SAM/CxCxxxxC-motif-protein-YfkAB	gnl\|CDD\|275271	TIGR04478, radical_SAM_superfamily_domain_protein, radical SAM/CxCxxxxC motif protein YfkAB. Members of this highly conserved family in some Firmicutes have an N-terminal radical SAM domain (pfam04055) and a C-terminal pfam08756 domain with a CxCxxxxC motif that suggests binding to an additional metallocluster. It appears all correct sequences in this family are about 370 amino acids in length, containing the YfkA and YfkB regions originally reported as separate ORFs in Bacillus subtilis. Partial Phylogenetic Profiling shows occurrences almost exclusively in the Bacilli, with very few examples of either lateral transfer or gene loss. The essentially monophyletic distribution suggests a housekeeping function. Members have no well-conserved gene neighborhood. The function is unknown. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP033687.1\|WP_035182334.1\|1944781_1945702_+\|SDR-family-oxidoreductase	gnl\|CDD\|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	3.29595e-162
NZ_CP033687.1\|WP_014095964.1\|1960930_1961116_-\|Fur-regulated-basic-protein-FbpA	gnl\|CDD\|315692	pfam13076, Fur_reg_FbpA, Fur-regulated basic protein A. This family of proteins is regulated by the ferric uptake regulator protein Fur. This family does not regulate the lutABC operon encoding iron sulfur-containing enzymes necessary for growth on lactate.	5.7044e-08
NZ_CP033687.1\|WP_110133851.1\|1952345_1954865_-\|ATP-binding-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	2.23882e-10
NZ_CP033687.1\|WP_035182336.1\|1943056_1944715_+\|isovaleryl-CoA-dehydrogenase	gnl\|CDD\|173843	cd01154, AidB, Proteins involved in DNA damage response, similar to the AidB gene product. AidB is one of several genes involved in the SOS adaptive response to DNA alkylation damage, whose expression is activated by the Ada protein. Its function has not been entirely elucidated; however, it is similar in sequence and function to acyl-CoA dehydrogenases. It has been proposed that aidB directly destroys DNA alkylating agents such as nitrosoguanidines (nitrosated amides) or their reaction intermediates.	1.88429e-143
NZ_CP033687.1\|WP_035182338.1\|1941549_1943073_+\|long-chain-fatty-acid--CoA-ligase	gnl\|CDD\|235730	PRK06187, PRK06187, long-chain-fatty-acid--CoA ligase; Validated.	2.56691e-166
NZ_CP033687.1\|WP_035182332.1\|1946148_1946976_-\|AAC(3)-family-N-acetyltransferase	gnl\|CDD\|376807	pfam02522, Antibiotic_NAT, Aminoglycoside 3-N-acetyltransferase. This family consists of bacterial aminoglycoside 3-N-acetyltransferases EC:2.3.1.81, these catalyze the reaction: Acetyl-Co + a 2-deoxystreptamine antibiotic <=> CoA + N3'-acetyl-2-deoxystreptamine antibiotic. The enzyme can use a range of antibiotics with 2-deoxystreptamine rings as acceptor for its acetyltransferase activity, this inactivates and confers resistance to gentamicin, kanamycin, tobramycin, neomycin and apramycin amongst others.	2.07927e-114
NZ_CP033687.1\|WP_035182340.1\|1941166_1941553_+\|MerR-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|133403	cd04776, HTH_GnyR, Helix-Turn-Helix DNA binding domain of the regulatory protein GnyR. Putative helix-turn-helix (HTH) regulatory protein, GnyR, and other related proteins. GnyR belongs to the gnyRDBHAL cluster, which is involved in acyclic isoprenoid degradation in Pseudomonas aeruginosa. These proteins share the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their conserved N-terminal domains contain predicted winged HTH motifs that mediate DNA binding, while the dissimilar C-terminal domains bind specific coactivator molecules.	2.10382e-36
NZ_CP033687.1\|WP_110133848.1\|1938554_1939298_+\|type-I-methionyl-aminopeptidase	gnl\|CDD\|237252	PRK12896, PRK12896, methionine aminopeptidase; Reviewed.	1.49157e-123
NZ_CP033687.1\|WP_014095974.1\|1948917_1949343_-\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	3.50502e-34
NZ_CP033687.1\|WP_014095963.1\|1961158_1961923_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|224561	COG1647, COG1647, Esterase/lipase [General function prediction only].	2.46148e-41
NZ_CP033687.1\|WP_035182331.1\|1947082_1948411_+\|polysaccharide-biosynthesis-protein	gnl\|CDD\|240529	cd13124, MATE_SpoVB_like, Stage V sporulation protein B, also known as Stage III sporulation protein F, and related proteins. The integral membrane protein SpoVB has been implicated in the biosynthesis of the peptidoglycan component of the spore cortex in Bacillus subtilis. This model represents a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	7.07445e-90
NZ_CP033687.1\|WP_014095965.1\|1959842_1960622_+\|Cof-type-HAD-IIB-family-hydrolase	gnl\|CDD\|319819	cd07517, HAD_HPP, phosphatase, similar to Bacteroides thetaiotaomicron VPI-5482 BT4131 hexose phosphate phosphatase; belongs to the haloacid dehalogenase-like superfamily. Bacteroides thetaiotaomicron VPI-5482 BT4131 is a phosphatase with preference for hexose phosphates. In addition this family includes uncharacterized Bacillus subtilis YkrA, a putative phosphatase and uncharacterized Streptococcus pyogenes MGAS10394 a putative bifunctional phosphatase/peptidyl-prolyl cis-trans isomerase. 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.	4.7271e-91
NZ_CP033687.1\|WP_061087166.1\|1939519_1940101_-\|biotin-transporter-BioY	gnl\|CDD\|376871	pfam02632, BioY, BioY family. A number of bacterial genes are involved in bioconversion of pimelate into dethiobiotin. BioY is a component of the BioMNY transport system involved in biotin uptake in prokaryotes.	4.4814e-35
NZ_CP033687.1\|WP_035182323.1\|1955089_1956151_+\|NAD(P)-dependent-alcohol-dehydrogenase	gnl\|CDD\|176188	cd05285, sorbitol_DH, Sorbitol dehydrogenase. Sorbitol and aldose reductase are NAD(+) binding proteins of the polyol pathway, which interconverts glucose and fructose. Sorbitol dehydrogenase is tetrameric and has a single catalytic zinc per subunit. Aldose reductase catalyzes the NADP(H)-dependent conversion of glucose to sorbital, and SDH uses NAD(H) in the conversion of sorbitol to fructose. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. The medium chain alcohol dehydrogenase family (MDR) have a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The N-terminal region typically has an all-beta catalytic domain. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit.	1.02091e-179
NZ_CP033687.1\|WP_014095966.1\|1959271_1959814_+\|SIS-domain-containing-protein	gnl\|CDD\|240138	cd05005, SIS_PHI, Hexulose-6-phosphate isomerase (PHI). PHI is a member of the SIS (Sugar ISomerase domain) superfamily. In the ribulose monophosphate pathway of formaldehyde fixation, hexulose-6-phosphate synthase catalyzes the condensation of ribulose-5-phosphate with formadelhyde to become hexulose-6-phosphate, which is then isomerized to fructose-6-phosphate by PHI.	3.66029e-41

>NZ_CP033687.1|WP_014095973.1|1949543_1949750_+|hypothetical-protein
MNENKKKSQRKMDNPEQFATENEDMHDKFMSEQTVDPIPMEDLREEKLEEKTDHDKKTTSSSEKKYKP
>NZ_CP033687.1|WP_014095974.1|1948917_1949343_-|universal-stress-protein
MFNRILVAIDGSKMSEKALKSALNFAKERFTKIGVIHVEKNPVIPEGMPNASIDTLYSEQQRDGDDLLDQAAALAEEEEIEIEKFYETGDPAAQIVRKAEEGNYQLIIMGSRGLGNLKGLMLGSVSQKVTQLAKCPVLIIK
>NZ_CP033687.1|WP_035182331.1|1947082_1948411_+|polysaccharide-biosynthesis-protein
MAVFFKGAFMLIGVAFIGECIEFLTNMVLANELGAHGMGLYMSILPAIFLIVTIASMELPISISKFVAEQEEKYHRDMLRFTIRLASLFVLLLMAAVALLLPVLPIFHHYHPYLRWLIIALIPMIAFSSIARGYFMGVQQMGKIAAANFLRKMMQLILLVLLFHWMEFDVQMSIFIAICTLVGSDLIVLLYLFHMFVLQMRTLKKKEQAPMGGKEIRRSLLSVSLPTTGMRVFHAVTNAIEPFFIKWVLLKSGMTEGMANEHFGLVAGVAFTIGFFPAFIAHSLSTVLIPTVSEAYAKRDGIKLQKLLQQVMMMTFLYGLPAVIVIQVFSVPLTTLFSHSAAAAVYVRLLWPYFLFHYFVIPMQAFLIGLGLVRDALAHFIWSTMVTYCLIYYLGSNPQYQMAGVIIAMNTGTLLIMMMHYLTICKKIEISLILRKSMKHTF
>NZ_CP033687.1|WP_035182332.1|1946148_1946976_-|AAC(3)-family-N-acetyltransferase
MTEENVIRQKQMLVTKERLVTDFRKLGLKEGMVVIVHSSLSALGWVCGGEVAVILALMEVVTERGTIVMPAQTANNTDPAFWENPPVPEAWWEEIRRSMPAFDPAVTPTYGMGRVAELFRTFPEVLRSHHPTCSFTAWGRDAKSILSGHSLDFPFGEKSPLARIYDRDGCILLLGVDYQVNTSMHLGESRSKHTKRCTQSCAMTINGKRVWQSYEDYEENSDLFNKIGRAFERSHQVKTGFIGAAPSRLIQQRALVDFTAQYLDELYTDTEKAHH
>NZ_CP033687.1|WP_035182334.1|1944781_1945702_+|SDR-family-oxidoreductase
MYWQKPDMYFSRTEPGYRNHPQKYAFPPQHQPEQPGIEKLMHPRPLIEDPSYKGSGKLENKVAIVTGGDSGIGAATAIAFAKEGADVVIPYYSNYEIEDAVRTKRRIEALGQRCLLIPGDLKDPEHCQNVVKQTVDTFGHLDVLVNNHAMQFVQKDLLNITNEQWDFTFKNNIHSFFYLVKAALPYLKAGSSIIFTSSVTAYEGNQNLIDYSATKGAIVAFTRALSQNLVRKGIRVNAVAPGPIWTPLIPASFYPEQVAKFGRDVPMKRAGQPYELAPTYVYLASRDSSYVTGQVLHVNGGTITGS
>NZ_CP033687.1|WP_035182336.1|1943056_1944715_+|isovaleryl-CoA-dehydrogenase
MNFYHDDPNLARLLKQYLDPLFFDWAEKELAEFGEMCAGEIDERATHTDREGQPKLIKYNRYGEDVSRVCVNEGYLKTVEQVYNKGIVGYVHKSIPALGQKGNYVYAFAQGYLLSQSEPGFYCPVTLTAAAAYLLDHYGSHELKQAYLPQLISTGEAERYEGATFLTERQGGSDVGANETKAVSEGGCYRLYGEKYFASNVGMCGVAMVLARREGAPSGTKGLSLFLVPWEKENGEKNGIYIRRLKDKLGVCAVPSGEVVFDGAKAYLVGDPRKGFYYMMEALNLSRICNAIASIGIMRRAYREARAYALRRTAFGSRLADYPMVKETLVKMAAKQEVETSAVFRLATLFDRTASGKADEQENIMTRLLIAILKMETAEQAIHFAHEAIEMHGGNGYIEDFVTPRLLRDAQVLTVWEGTANILGLEVLRLMRKFKVHDIFIGMMREKIDQLQAGTWLSAGLDQLEETCRFVMETKEEAAQTYHCKKVARQMVKIYESVTALEDALAGQRQKWIAEAYLRLAWHDPLAIDPELALVKHFEEIVMEKVPANEGN
>NZ_CP033687.1|WP_035182338.1|1941549_1943073_+|long-chain-fatty-acid--CoA-ligase
MNISELLARNARKYPQQEALVSPRERLNYQELNVRVNRLAHALQNCNFKQGDRAVIVMPNTNAFVIAYFAVMRLGGIVVPVNAKSSRAELEYMLDDSGANVLFVHELLFEELKEATFPPHLVKIKTGERVTGCQIFEEMINHSPETEIRCRLKEDDDASILYTSGTTGKPKGVLFTNRNILSAAWMMCVEMAMKPESRILHMMPLSHSAPLHLFLVAGTVVGATHVLSPVFTPEALVETVEKERITHFFGAPVAYLFTAKLPNLQDYDLSTMKYWVYGGAPLSRPEVGLIQNAFRSDRLVCVYGLTEAGPNGTLLLPEEHAEKAGSIGKRAALGMEIRLVNEKGEDVAAGEVGEIALYGESVMKGYFRKPEETNRVFQNGWLLTGDMARKDEEGYYWVVDRKKDMILSGGVNVYPKEIEDVLVTHPKIREVSVIGVPHPEWGETVKAFLVLAEPMDNIEEECKRFLKGKLASYKIPKLYERIEELPRNATGKIQKQVLRGKANELLP
>NZ_CP033687.1|WP_035182340.1|1941166_1941553_+|MerR-family-DNA-binding-transcriptional-regulator
MTCKISELAAEFGVSTRTIRYYEELGLFKPKRSQNGRRCYSKKDYTRLKLIFRGKQLDFSLDEIKEMIELFDCDRSGIKQLKKTIEYGKQKRREVAQQIQNLQELQSELEKYLAEFETRLKRLKEEQG
>NZ_CP033687.1|WP_061087166.1|1939519_1940101_-|biotin-transporter-BioY
MAAKKFRAIDLCYAGMFAALMAIGANITSIAPFLVIGGVPITLQTFFAVLAGLVLGSRLGAISMVAYMLIGLLGAPVFAQFSGGFQTVLSPTFGFILSFIPAAWATGKIVEKRQNLTTYFIAAIIGLILNYLIGTNWMYAAYKIWAQAPQAFSYKIAWVWMAVPLPKDIVLSLVAGWLAHRIKAVSPLIALKR
>NZ_CP033687.1|WP_110133848.1|1938554_1939298_+|type-I-methionyl-aminopeptidase
MIVKSEADLEGLKKIGRLVASIRDELKEKARPGITTKELDEWAGKRFAENGAVSGPMGEYDFPGYTCISVNEEVAHGIPGDRVLKEGDLVNVDVSGSLDGYYADTGISFVVGKGDPELFALCECAQLAFDSGLKKIRAGNRQNQIGRAVEKAVYDNGFEVLLNLTGHGVGKALHEDPEYILNYYDPDDTGLLQDGMVIAFEPFVSTGADEVVESGDGWTYVTPDGSFVAQVEHTVIVTKGTPIVLTQ
>NZ_CP033687.1|WP_110133849.1|1950146_1950743_-|hypothetical-protein
MGWFIGIIIIILLVYFLIIRPLIERNRPQIIEPRRSIYNGDAYDPHPEQTGWNDGGNAGIGRFGMFAGGMATGALLTYLLEQGRIGLDQFEHFQNLDGNDLLQELEEQNILQQDEIDHLQDTLSNFEDNGHDGHEDGDHGDHDQQDTGFDLAHFSSHEDHDTHDNDQQDTGFDLADFSSNDDNDFGGWDSGSDDNNWL
>NZ_CP033687.1|WP_110133850.1|1950893_1952045_-|radical-SAM/CxCxxxxC-motif-protein-YfkAB
MLKEETQRSITPEYDPWEAYMDITTHGKLTLSNIEFTTTTLCNMRCEHCAVGYTLQPKDPDALPLDLLLRRLDEISTLRCISITGGEPMLSTKSVENYVLPLLQYAHERGIRTQINSNLTMKLEKYVQIAPYLDVLHISHNWGTVRDYIDGGFANMRIKPSDQHGEKLFRRIVENSRALSEMGVMVSAETMLNKRTLPYMEQIHHQIVEEMKCARHEIHPMYPSDFAADLEVLSLDEIRKAIHHLLDIRDESVWMLFGTLPFYPCSPNPEDQALLKRLYESKNVTLRNDPDGRSRLNVNIFTGDVIVTDFGDTPPLGNIQHDRLPDVFEKWLETPIAKSLNCHCPQVKCLGPNILVKNAYYKNIDFTQRKAVIDMQGASSRMG
>NZ_CP033687.1|WP_110133851.1|1952345_1954865_-|ATP-binding-protein
MAELENQKKFSSLLSSGVKALKQHPDYKTNREAGNKTGQSYMEKIAYKLGVSPNTVKSWIGQMGSKYIPGRIEDAKLFGIIWLILEKGCMNVTWFMELLETTSIPVIEPALPAWVASCLKKAKTMNDNGTIGTPPPEEINMVITRLFGNAAVLESEEKNKFSAHNLPARWSGRFIGRKSDLQAIYHWLLSPSPVCSITGWAGVGKTTLALEAAYACAGEPGEEAANVSDKWPAFHCIIWFSTHLTGLSFNDFLNTIAYQLGLTEQIDKPVMEKRFAVRHALQLFSREQPILLIVDSMDAAEKEVLEFIINLPQGVKAMLTSRENYNQDYKDAFQNFTIVKLKGLNEKEALSYLSFVIREHLQTGSAPNQEELRHLTPEMQAKLIKAAAGNPKALSLCIAYISDGGIPAEQLIQEIESAGYSLLELFEFLFGRTWKRIDEAARRLWQVLCFFEKPPVEAAWAAAAGLDARGFYAAVEQMRNYALIHPDRTDGKLRYPAHQTVIAYGEQHLSENRQLEKEARKRWARYYIHFLDTHLKREQPNIFYWRYLLGRDLDDLKQEWTNIRKVMEWASQSDEKEILIEFVVRTSHFLSRVNLPLRVEYGRKAADFAAALDKSMLEAFFRIDTVGWALMEMNELEEALIQIDAGLKRLSGLDAGNEDTRDLMVWGHALKSRVLLKAGDPDQAEAILSKVIPVPSTPMIRHRVLLVQGDLYLERKKYKEAIRAYEAANQISHAYGGEKTIEAYFNLGIAYVENQQFEKAAAAFEKMLYQKNKANPIELMYYHYGMARLFAKKGDLAYALYSSQEALHLAASWEQNISIRDETEKFNQFIKKKIQYQNR
>NZ_CP033687.1|WP_035182323.1|1955089_1956151_+|NAD(P)-dependent-alcohol-dehydrogenase
MTNHIPETMKAAVMHGTRNISIETLPVPQIEENEVLIKVMAVGICGSDLHYYETGRIGKYVVDKPFILGHECAGEIAAVGSKVRHFKVGDRVAVEPGVTCGHCEACKEGRYNLCPHVQFLATPPVDGAFCQYIKMREDFVFAIPDALSYEEASLVEPFSVGIHAATRTKLQPGSTVAIMGMGPVGLMAVVAARAFGASNIIVTDLEPLRLEAAKEMGATYAINIREQDPYEAIQDITNGKGVDVAWETAGNPAALQSALASVRRGGKLAIVGLPAQNEIPLNVPFIADNEIDIYGVFRYANTYPKGIKFLASGIADVKKLVTDQYALEDTYQAMERALNFKNECLKVMVYPNN
>NZ_CP033687.1|WP_014095967.1|1958179_1959139_+|LacI-family-DNA-binding-transcriptional-regulator
MTNIRDLAKMAGVSVTTVSRVLNNHPYVSEEKKNAVLKAVKATRYHKNINAVHLSKGKTKLIGVVLPFTDHPYFALLLKGIAKQALEYNHKLLLFQTDYMESRETEALQMLQQKQIDGLIICSRACSMRKIEEYLPFGPIALCECVKGGEISSTYIDHYKIFMDALEFLYRKGHTKIGYCIGRKSGTNSRNRDKAYWDFHEKYHLPHHPEYIFDQCYDYEDGERVLSRVKEMDPPPSALLVTSDQVAAGIVISCNKQQISIPDELAIIGFDNEPIAGMLNITTIDIPLVEMGRNLVHQVLTKEIKNKEISATLIERGTV
>NZ_CP033687.1|WP_014095966.1|1959271_1959814_+|SIS-domain-containing-protein
MNILEDAKAMVLELYASLCSKVDDQPLEQVVEVIGRSNRLFLAGTGCSEMILRVFANRLVHLGFRVGMIGDLISPVPKKGDTILFSSKSGENPVLLNAARKAKLHGINIVAITASPASTLAKMADVTVLLPDESSEFESIKQAGLTPDRIGTLFELLSFLIYDVITASLMKKRHPENEYA
>NZ_CP033687.1|WP_014095965.1|1959842_1960622_+|Cof-type-HAD-IIB-family-hydrolase
MKQQSVIFFDIDGTLLTHEKKLPVTTKKAIDKLKSDGHVTAIATGRAPFMFEDLRKELGMDTFVSYNGQYVVMNGEVLFKNPLNRQSLEELTAYALSHQHPLVYMDHEDMKANVPNHEDIEKSITSLKIGRLPAYDPHYYKGRELYQALLFCSEGEEKQYEQAFPDFEFIRWHPLSVDVLPKGGSKARGIEKIVEKLGFPPERQYAFGDGLNDIKMLSMIKNSVAMGNAEEKVKAAAKYITKSVEDMGIPHGLQIVGLL
>NZ_CP033687.1|WP_014095964.1|1960930_1961116_-|Fur-regulated-basic-protein-FbpA
MKNFLRHAIEKKRQYLIEQLIALGAYQEDDKQLFTLTLTELETEYAYFSKISQEKEASGRE
>NZ_CP033687.1|WP_014095963.1|1961158_1961923_-|alpha/beta-fold-hydrolase
MHEYYPVLSGAESFFIKGNEIGILISHGFNGTPQSVRFLGEALASDGFTVCAPRLKGHGTHILDMERCTYKDWIASLEEGYQLLKRHCHDIFVIGQSMGGTLALHLAEKHPDIRGIVCINAAIQSIPELEKCLAKGRFIQEGPPDIKAAGVHEISYEKVPVASIRELLSVMWETRENLSAIHCPALLFQSTEDHVVPPENTEYIAAHIHASRKKIVPLRNSYHVATMDHEKEWIAAQCSLFVQEIAHIETRTEI
>NZ_CP033687.1|WP_104851256.1|1962108_1964211_-|class-I-SAM-dependent-methyltransferase
MADLLSSLKLIAKAKAGNTDILHEHKWLSYLYRTDEKNVNLEQVESLENLEPNPVLHYVEKTLAILDRCYADLPASEKEIIEEVLRWSEVAKCGSAQKREEWRRRGFQLRIHNIGSARIYAHEQMAVPFGQRHLQKEDLIYTLILTHGLVGQFIRGEVRYRQLYPLIDWIQSHRSSLKWDIKRILLALNHCIIEGVSPAIWEKVRAETSQITSWIAAGEKSREHSLKERLRRLRESSIQKGEDFEALYTKWFSNRELASMFHLLFQKTDIWYVESALQDFSFEEFLKIFLLVYQKTNPLTVEQISFEPLMKDIYYDYKGKKSVNLYKKRIIEAYLKACPLAGLISGDTQPNEHVTLELIPFDSLGSATGVNFTFSKPGEKLIAFCQEAEKSPLYERSILLLYDFFGFRKDAFDRLQNEQHYLADMNNAEDHKKIIADFAKGTVMIDVGAGGGIMLDLLSEKHPDADITGIDISTNVIQELERKKVRERKSWKVKQADALKLSSYFELESADTIIFSSILHEMYSYIPFHGRTYNPDVVKAALKSAFAVLKPGGRMIIRDGIMTEPKDLIRLLAFRDPDGFRFFTRYVEDFKGRKIDYEITEDNKIKLPVNDLMEFLYTYTWGEEAYPHEVQEQFGYFTPSEYRKVIEETLGSRANIICFRHYLQEGYSTHLLPKVKVMDESGKETALPDSTCFIVIEKAE

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Crispr_ID: NZ_CP033687_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_10

2131656-2131734

Orphan

Consensus_repeat	Method
TGAAAGACATTTTATAGGGTGGCTGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_10

>merge|NZ_CP033687|10|2131656-2131734|CRISPRCasFinder
TGAAAGACATTTTATAGGGTGGCTGCCAGTATTTTGTCCTTCATCCCCTTGGTGAAAGACATTTTATAGGATGGCTGCC

>NZ_CP033687|10|9|2131656-2131734|CRISPRCasFinder
TGAAAGACATTTTATAGGGTGGCTGCC	AGTATTTTGTCCTTCATCCCCTTGG
TGAAAGACATTTTATAGGATGGCTGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_014095829.1\|2126381_2127197_+\|prolipoprotein-diacylglyceryl-transferase	unknown	unknown	gnl\|CDD\|183527
NZ_CP033687.1\|WP_035182145.1\|2121630_2122776_+\|DUF4097-domain-containing-protein	unknown	unknown	gnl\|CDD\|226123
NZ_CP033687.1\|WP_014095815.1\|2140279_2140486_-\|alpha/beta-type-small-acid-soluble-spore-protein	unknown	unknown	gnl\|CDD\|365990
NZ_CP033687.1\|WP_014095819.1\|2135544_2135814_+\|HPr-family-phosphocarrier-protein	unknown	unknown	gnl\|CDD\|172320
NZ_CP033687.1\|WP_110133865.1\|2128557_2130069_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP033687.1\|WP_110133866.1\|2130251_2131199_+\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP033687.1\|WP_013858128.1\|2123739_2125050_+\|transposase	unknown	unknown	gnl\|CDD\|379382
NZ_CP033687.1\|WP_017551706.1\|2127942_2128458_+\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP033687.1\|WP_014095823.1\|2132037_2132496_+\|8-oxo-dGTP-diphosphatase	unknown	unknown	gnl\|CDD\|239519
NZ_CP033687.1\|WP_035182139.1\|2135900_2136485_-\|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	unknown	unknown	gnl\|CDD\|178955
NZ_CP033687.1\|WP_104851288.1\|2122894_2123245_+\|phage-holin-family-protein	unknown	unknown	gnl\|CDD\|224861
NZ_CP033687.1\|WP_110133870.1\|2138835_2140224_+\|class-II-fumarate-hydratase	unknown	unknown	gnl\|CDD\|234779
NZ_CP033687.1\|WP_014095822.1\|2132532_2133423_+\|RNase-adapter-RapZ	unknown	unknown	gnl\|CDD\|235450
NZ_CP033687.1\|WP_110133868.1\|2137142_2138069_+\|transposase	unknown	unknown	gnl\|CDD\|273806
NZ_CP033687.1\|WP_013858691.1\|2134480_2135434_+\|DNA-binding-protein-WhiA	unknown	unknown	gnl\|CDD\|273194
NZ_CP033687.1\|WP_110133869.1\|2138065_2138365_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273806
NZ_CP033687.1\|WP_061086719.1\|2133419_2134400_+\|YvcK-family-protein	unknown	unknown	gnl\|CDD\|211689
NZ_CP033687.1\|WP_110133864.1\|2127292_2127946_+\|pyrophosphatase-PpaX	unknown	unknown	gnl\|CDD\|237336
NZ_CP033687.1\|WP_110133863.1\|2117734_2121331_-\|GW-domain-containing-glycosaminoglycan-binding-protein	unknown	unknown	gnl\|CDD\|367953
NZ_CP033687.1\|WP_014095830.1\|2125364_2126318_+\|HPr-kinase/phosphorylase	unknown	unknown	gnl\|CDD\|235459

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_014095829.1\|2126381_2127197_+\|prolipoprotein-diacylglyceryl-transferase	gnl\|CDD\|183527	PRK12437, PRK12437, prolipoprotein diacylglyceryl transferase; Reviewed.	2.86191e-137
NZ_CP033687.1\|WP_035182145.1\|2121630_2122776_+\|DUF4097-domain-containing-protein	gnl\|CDD\|226123	COG3595, COG3595, Uncharacterized conserved protein [Function unknown].	1.5029e-25
NZ_CP033687.1\|WP_014095815.1\|2140279_2140486_-\|alpha/beta-type-small-acid-soluble-spore-protein	gnl\|CDD\|365990	pfam00269, SASP, Small, acid-soluble spore proteins, alpha/beta type.	7.24679e-25
NZ_CP033687.1\|WP_014095819.1\|2135544_2135814_+\|HPr-family-phosphocarrier-protein	gnl\|CDD\|172320	PRK13782, PRK13782, HPr family phosphocarrier protein.	9.16542e-41
NZ_CP033687.1\|WP_110133865.1\|2128557_2130069_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	2.3462e-12
NZ_CP033687.1\|WP_110133866.1\|2130251_2131199_+\|thioredoxin-disulfide-reductase	gnl\|CDD\|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	1.09997e-153
NZ_CP033687.1\|WP_013858128.1\|2123739_2125050_+\|transposase	gnl\|CDD\|379382	pfam13808, DDE_Tnp_1_assoc, DDE_Tnp_1-associated. This domain is frequently found N-terminal to the transposase, IS family DDE_Tnp_1, pfam01609 and its relatives.	1.83346e-09
NZ_CP033687.1\|WP_017551706.1\|2127942_2128458_+\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	5.96808e-31
NZ_CP033687.1\|WP_014095823.1\|2132037_2132496_+\|8-oxo-dGTP-diphosphatase	gnl\|CDD\|239519	cd03427, MTH1, MutT homolog-1 (MTH1) is a member of the Nudix hydrolase superfamily. MTH1, the mammalian counterpart of MutT, hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP and 2-hydroxy-ATP, to monophosphates, thereby preventing the incorporation of such oxygen radicals during replication. This is an important step in the repair mechanism in genomic and mitochondrial DNA. Like other members of the Nudix family, it requires a divalent cation, such as Mg2+ or Mn2+, for activity, and contain the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as a metal binding and catalytic site. MTH1 is predominantly localized in the cytoplasm and mitochondria. Structurally, this enzyme adopts a similar fold to MutT despite low sequence similarity outside the conserved nudix motif. The most distinctive structural difference between MutT and MTH1 is the presence of a beta-hairpin, which is absent in MutT. This results in a much deeper and narrower substrate binding pocket. Mechanistically, MTH1 contains dual specificity for nucleotides that contain 2-OH-adenine bases and those that contain 8-oxo-guanine bases.	8.94661e-41
NZ_CP033687.1\|WP_035182139.1\|2135900_2136485_-\|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	gnl\|CDD\|178955	PRK00277, clpP, ATP-dependent Clp protease proteolytic subunit; Reviewed.	8.2757e-150
NZ_CP033687.1\|WP_104851288.1\|2122894_2123245_+\|phage-holin-family-protein	gnl\|CDD\|224861	COG1950, COG1950, Predicted membrane protein [Function unknown].	6.83396e-21
NZ_CP033687.1\|WP_110133870.1\|2138835_2140224_+\|class-II-fumarate-hydratase	gnl\|CDD\|234779	PRK00485, fumC, fumarate hydratase; Reviewed.	0
NZ_CP033687.1\|WP_014095822.1\|2132532_2133423_+\|RNase-adapter-RapZ	gnl\|CDD\|235450	PRK05416, PRK05416, RNase adapter RapZ.	1.79928e-176
NZ_CP033687.1\|WP_110133868.1\|2137142_2138069_+\|transposase	gnl\|CDD\|273806	TIGR01784, Uncharacterized_protein_pSLT051, conserved hypothetical protein (putative transposase or invertase). Several lines of evidence suggest that members of this family (loaded as a fragment mode model to find part-length matches) are associated with transposition, inversion, or recombination. Members are found in small numbers of genomes, but in large copy numbers in many of those species, including over 30 full length and fragmentary members in Treponema denticola. The strongest similarities are usually within rather than between species. PSI-BLAST shows similarity to proteins designated as possible transposases, DNA invertases (resolvases), and recombinases. In the oral pathogenic spirochete Treponema denticola, full-length members are often found near transporters or other membrane proteins. This family includes members of the putative transposase family pfam04754.	5.23353e-12
NZ_CP033687.1\|WP_013858691.1\|2134480_2135434_+\|DNA-binding-protein-WhiA	gnl\|CDD\|273194	TIGR00647, DNA_bind_WhiA, DNA-binding protein WhiA. This family describes a DNA-binding protein widely conserved in Gram-positive bacteria, and occasionally occurring elsewhere, such as in Thermotoga. It is associated with cell division, and in sporulating organisms with sporulation. [Cellular processes, Cell division].	8.58946e-147
NZ_CP033687.1\|WP_110133869.1\|2138065_2138365_+\|hypothetical-protein	gnl\|CDD\|273806	TIGR01784, Uncharacterized_protein_pSLT051, conserved hypothetical protein (putative transposase or invertase). Several lines of evidence suggest that members of this family (loaded as a fragment mode model to find part-length matches) are associated with transposition, inversion, or recombination. Members are found in small numbers of genomes, but in large copy numbers in many of those species, including over 30 full length and fragmentary members in Treponema denticola. The strongest similarities are usually within rather than between species. PSI-BLAST shows similarity to proteins designated as possible transposases, DNA invertases (resolvases), and recombinases. In the oral pathogenic spirochete Treponema denticola, full-length members are often found near transporters or other membrane proteins. This family includes members of the putative transposase family pfam04754.	5.96615e-05
NZ_CP033687.1\|WP_061086719.1\|2133419_2134400_+\|YvcK-family-protein	gnl\|CDD\|211689	TIGR01826, Putative_gluconeogenesis_factor, conserved hypothetical protein, cofD-related. This model represents a subfamily of conserved hypothetical proteins that forms a sister group to the family of CofD, (TIGR01819), LPPG:Fo 2-phospho-L-lactate transferase, an enzyme of cytochrome F420 biosynthesis. Both this family and TIGR01819 are within the scope of the pfam01933. [Hypothetical proteins, Conserved].	2.26937e-159
NZ_CP033687.1\|WP_110133864.1\|2127292_2127946_+\|pyrophosphatase-PpaX	gnl\|CDD\|237336	PRK13288, PRK13288, pyrophosphatase PpaX; Provisional.	7.42072e-127
NZ_CP033687.1\|WP_110133863.1\|2117734_2121331_-\|GW-domain-containing-glycosaminoglycan-binding-protein	gnl\|CDD\|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	2.20836e-92
NZ_CP033687.1\|WP_014095830.1\|2125364_2126318_+\|HPr-kinase/phosphorylase	gnl\|CDD\|235459	PRK05428, PRK05428, HPr kinase/phosphorylase; Provisional.	4.80834e-174

>NZ_CP033687.1|WP_110133866.1|2130251_2131199_+|thioredoxin-disulfide-reductase
MSEEQIYDVIIIGAGPAGMTAAVYASRSDLKTLMIERGVPGGQMVNTEEVENYPGYESILGPELSNKMFEHAKKFGAEYAYGDIKGIEIDGDYKIVKAGAKAYKALAVIIATGAQYKKLGVKGENELGGRGVSYCAVCDGAFFKGKDLVVVGGGDSAVEEGNYLTRFANKVTIVHRRDQLRAQKILQDRAFKNEKIDFIWNHTVKEIHEENGKVGSVTLVSTVDGLEKPFKTDGVFIYIGMVPLTKPFENLGITNEAGYILTNEEMETKIPGIFAAGDVREKTLRQIVTATGDGSIAAQNAQHYVEEVKEAMKAG
>NZ_CP033687.1|WP_110133865.1|2128557_2130069_+|tetratricopeptide-repeat-protein
MSKDSKLRQEHDNVLSFVPTGEYYFNKGVQAYDRHDIKKALKYMQRAAQLDPYDPVIACQLAIIYTHCEAFRKAIDIFRHILAKLDPGMVECHYFIANNYADLGFFNEALYHARKYLELDPFGEYREEAEELIYVLDLEEEDETGAISYEQDELMARQEEARRYLEAGHFDTALSELHKLIKKYPDFWSAYNNMALACFYLGQTEKAVEVLMDLLEKNPGNLHALCNLAVFYYHKRDDEKLEQILRGLEKVRPVLLDHQYKLGATFAIVGCYEEAYLWLNRLKKVGFDGDASFYYWLSRAAYHTNRQQAAEAAWEQLVELNPEKKGCEPWNREMKKKMNEKNVQFILDRLNSTELSERFFGIFMIGLSSNRSDIVSHPDFKPLDDFTLTEKIYLAHVLESDIRESFDPDEVFVRGHNIACILHSHYGPMFPGYTNLMLAWFSIFLTGLKRGERFQNESGFAAAIDYLWHHQKGDKVSQQAIAREYRISVSTLRKYANRIKSLL
>NZ_CP033687.1|WP_017551706.1|2127942_2128458_+|acyltransferase
MRNTKRYPVKGSNALWQIYKTVSFWKVFKNVLVIEIARFLPFLRFKNQMYRTFLHMQVGDRTAFAYKALVDILFPEMITVGKNCVIGYHTTILAHEYLIDEYRIGEVVIGDDVMIGANTTILPGVTIGDRAVVAAGSVVHKDVPAGAFACGNPLQIRQKSSEKKDPEQTKR
>NZ_CP033687.1|WP_110133864.1|2127292_2127946_+|pyrophosphatase-PpaX
MKNRITTLLFDFDGTLIDTNELIIQSFLYTLNDYYPGRYSREDVLIFNGPPLIDTFLSIDPERAEEMTAKYRAYNIQQHDALVKEFPGVYDTIKMLKEHRFKLGIVSTKMKDTIKKGLKLAKLDPFFDVIVALDDVKKAKPDPEPVQKALRLLDSKPEEAMMIGDNYHDIEAGKNAGTFSAGVAWSAKGRAFLEQYNPDFMLETMTDLAEIVGVHVK
>NZ_CP033687.1|WP_014095829.1|2126381_2127197_+|prolipoprotein-diacylglyceryl-transferase
MDSNITPLNPIAFHLGGFSVHWYGIIIGCGILLGLALAMREADRLSVDQNIIADLCIWAIPVSIICARIYYVLFEWEYYAQHTSEIIKIWNGGIAIHGALIGAVVTAILFTRAKGVSFWKIADIVAPSLILGQAIGRWGNFMNQEAHGRAVSRAFLENLHLPDWIINQMYINGTYYQPTFLYESLWDLAGFIFLLLLRRRAAMHRGEIFLTYLIWYSIGRFFIEGLRTDSLMLTAHIRMAQVVSFILIVCALLLWFYRRKTGLSAKRYDEE
>NZ_CP033687.1|WP_014095830.1|2125364_2126318_+|HPr-kinase/phosphorylase
MAKVRVADMIKHFNLELISGEEGIHRPITTSDISRPGLEMTGFFDYYPADRIQLLGMTEITFSKRLSPEERKSRMDNLCSDITPGIVISRNLEVPDELIEASEEKSIPVMRTPMKTTRFSSRLTNYLEYKLAPATAIHGVLVDVYGVGVLITGKSGVGKSETALELVKRGHRLVADDCVEIVQEEEGSLIGHAPELIEHLLEIRGLGIINVMTLFGAGAVRSHKKITMIANLELWDEHKQYDRLGLDEEKVKILDTEITKMTVPVRPGRNLAIIIEVAAMNYRLKNMGVNAARQFTAKLANVIEEHEQGTEEEKNEP
>NZ_CP033687.1|WP_013858128.1|2123739_2125050_+|transposase
MVTRKEKRNREKEANYFFEFLKIQKHFFKDLMNNLKKVADHRHQSYITYGPEVLLFTMMLKNMTGLKSMRNMSESFNKEECIKNVGKVLGLDSLEELPHYDTINDFLSGLDVNELEKIRTYMIKELLKKRSLESYRIEGKYWGVIIDGTGLHTFHEKHCKHCLRRAYTNKETGETNVLYMHHVLEAKLVVGDMVFSIASEFIENESENVSKQDCELKAFDRLAKKIKKIFKRLPICILGDSLYACETVFNLCRAHKWKYICRFKEGRIKSISTEFKAIKELEQSKDQNSLVWVNDIAYKDRTVNLMEATMKTEDGKSKEYVFITDIKITKKNVERLIAAGRSRWKIENQGFNEQKNNRYNIEHANSQNYTAMKNHYLLVQITDIIRQLFEKGSSILKALKKTAKEKSSNLLESFRTRILTDEDFTHLSKPIQVRFT
>NZ_CP033687.1|WP_104851288.1|2122894_2123245_+|phage-holin-family-protein
MIMRWLLGILINAALFIALSGYFHGFYVENIGAAVMSSLVLSILNILVRPILILLTLPITILTLGIFLLVINAITLVLTDELMGASFEIDSFGMAFFVAIIMAIVNLILQETVFRK
>NZ_CP033687.1|WP_035182145.1|2121630_2122776_+|DUF4097-domain-containing-protein
MENKRKRILDMVKDGKLSTDEALTLLEALDREEAGQIAAKEDPAENGEQATNGGSGEAGSTTGQKKFRDADRNFNETKEKLFDLVGGALKKIKDFDLQLGQSAEVSHVFQQSLPETDTIELDIANGHLTFKQWDQEDVRIECQAKVYRTNDREDARSFLLNNSTFSVEGGRLVFSTQSKWMKVDTAVYVPASRYRKITLSTFNGNVQVKDIQADQLKVKTLHGKVLVEHADLETAEVETGNGTVDFDGNTIGQVEVQTMNGDIRWNGACRRSDFEAFNGNITVKMAPGADSLHSKTVSGNIEMTIPENISVHGEGKSNFGNFAIDLQGMEKYEERKEMIQKVARFSRKGTTEPALYIFADAKTGSITINEQTPDEEESPEA
>NZ_CP033687.1|WP_110133863.1|2117734_2121331_-|GW-domain-containing-glycosaminoglycan-binding-protein
MNKKVLKRRLKFIGAPIIQYLIKDNHQRANQYAKFYDQLRIKPNTILYESRDGKSMTDSPYAIFKYMVDNPAYQHYNHIWSIQDFQSLQPVIDKYKKYPNVKFVQRNSREYLKELASCAYLINNSTFQSFYAPKKGQVYINTWHGTPLKSMGFDIPGNPAQSQNVLRNFLSADYLLSPNEHTTKMYLDSYKLEGLYDGKIIEEGYPRIDLTFHTNPNTVKKALKDAGLTVDFNKKNLLYAPTWKGKSVSKANNDVMQIISDMDRVEKEAGNEYNVFVKVHPFLYPQAAKYPELQSRLVPDYMDTNELLAATDLLITDYSSIFFDYLVTGKPILFYTWDYDVYSEERGQYLKNEDLPGPLLFSVEQLIEAIHNIETVSQKYASNYQNLRSRFTNHEDGKVTERIVQYIFDQASLPLHIVNAVPVKKERILIYPGGMRNNGITSSFLNLMNNIDFEKYDVSCFTGAPRSKEVLNNIYKINKNVRMIFKPGVPLYRVFEVYRDKFTHNRGIQGNLGKKIFPERAYVREHTRLFGNSHFDYIIDFSGYSYYWAKYLVVADAKRKICFMHNDLLSDSEREINGKHPHRINLRGLFTLYYRFDKLVSVSKGTMEVNRKNLSRYANDDQFDYVLNSINPDRILYAEEEKSDEPKITKFKARALLSNVNDYPVWRVLPSIEGATQVSLSNEMANAEVLITAKSTVKHALYYRFHYEGKEIGWIHEKAVALLPDSVVTSEKVDKLAKIVKTRGNAIWSKPFKLPGTRKISLSSDFKNCIVAVDQAVQTQHSTYYRFSVKKEAIGWIDKRALGFYSSCTIEPNTGIFSKLEIFVLRKLIQTLNYSKREFLNHLDGRTRRLVDLRKPKYYKVAGSVNEPIWNKPYPNHKAKMVEEALNYKDAIVTVKKLAKTKQGVYALIYLKNNKIGWIHTSALSPLKRSTVVSDIEVLKIARILPDEKNAVIWSKPYGMEGAEKAGLPDMLKGDATFTIDREVTTPSGTYGRILQADGPEIGWINMRNVFVERAYGYEVNGQYVPEPDSSHYNFVNMGRLSPEKAQANLISAFADFHKNHPKSKLYILGQGPLKAELQALILELGVSDSVFLMGQLDNPFPFMKKCDCFVLSSHYEGQPMVLLEALTLGMKIVATDIVANRTVLEDGKYGLLVEDSINGLKSGLEAMITHQHPEFEKFHYQAYNKAAMETFYRCLHE
>NZ_CP033687.1|WP_014095823.1|2132037_2132496_+|8-oxo-dGTP-diphosphatase
MQRITNCVFIKDGQVLLLQKPRRNWWVAPGGKMEQGETVREAVIREYREETGIYLKHPDLKGVFTIVIKDGDKPVSEWMMFTFVATDGDGKNFEQSAEGILQWHAIDEMKNLPMAAGDTHILEYMVHGSGIIYGQFTYTPDFELLSYRLDPS
>NZ_CP033687.1|WP_014095822.1|2132532_2133423_+|RNase-adapter-RapZ
MGLEGNQMQFVIITGMSGAGKTVAIQSLEDLGFFCVDNLPPTLLPKFLELMKDASNKMNKVALVMDLRGREFFDDLFRALDELDKSSWVTPTILFLDADDSVLVRRYKETRRSHPLSPDGTPLEGIQQERKILEELKGRAQLILNTSNLKPRELREKIVMEFSANKQSFFTVNVLSFGFKNGIPIDCDLVFDVRFLPNPFYIEHMRPKTGLDEEVYTYVLKWNETQKFLEKLTDLLAFMLPHYKREGKSQLVIGIGCTGGQHRSVALAEYIGHFFEKDYHTTISHRDIKRKEERKP
>NZ_CP033687.1|WP_061086719.1|2133419_2134400_+|YvcK-family-protein
MRHPKIVLIGGGTGLPVLLRGLKKYPVEISAIVTVADDGGSSGRIRNEMDIPSPGDIRNVLAALSDVEPLLEKMFQHRFETGDELSGHSLGNLIIAALTSITGDFVHAVKELSKVLNVRGQVLPSANQSVVLHAEMEDGSIVSGESKIPCAGKKIKRVFLTPEVIQPLPETLTAIQEADLIVIGPGSLYTSILPNLMVPGLGEAVCQAHAKKVYVCNLMTQAGETNHYTAADHVQAILNHMGSACIDTILVNDEDVPEPVMSRYREELAQPVVYDVKRLMGLGLEVVSGNILTYKGGVIRHDTEKVAEILYDILKKQQWLSRSSAR
>NZ_CP033687.1|WP_013858691.1|2134480_2135434_+|DNA-binding-protein-WhiA
MSFASEIKKELTNLAVKDCCVRSELSALIRMNGSLSFSNKVLVVNVQTENAAIARRIYVLVKRLYDVPVELLVRKKMRLKKNNVYIVRLKARAKEILEDLHILGEHFTFTRNISPELLKKKCCKRSYLRGAFLAGGSVNNPETSSYHLEISSQYKEHNDALCRLMNGFHLNSKTLERKKGYITYLKEAEKITEFLNIIGAHHALLRFEDVRIVRDMRNSVNRLVNCETANLNKTIGAALRQVENIRYIEETVGLDALPEKLREIAVLRVNHQDVTLKELGEMVSGGHISKSGINHRLRKIDEIAEKLRANGPANKNS
>NZ_CP033687.1|WP_014095819.1|2135544_2135814_+|HPr-family-phosphocarrier-protein
MIEKQLEVKLKSGLQARPAAQFVQEATRFSSEIFLEKEGRKVNAKSIMGLMTLAAGHGETVTLSVDGSDEEEAFEHLANYIEGKEKLPS
>NZ_CP033687.1|WP_035182139.1|2135900_2136485_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP
MNLIPTVIEQTNRGERAYDIYSRLLKDRIIMLGSAIDDNVSNSIVSQLLFLEAENPEKDIYLYINSPGGSVTAGLAIYDTMQIIKPDVQTICVGMAASMGSVLLTAGTKGKRYALPNSEVMIHQPLGGAQGQATEIEIAAKHILYTRAKLNKILSDHTGQPIEVIERDTDRDNFMSAEKAKEYGLIDHIMTKKN
>NZ_CP033687.1|WP_110133868.1|2137142_2138069_+|transposase
MELVMEKHAGYHVHDRFFKELIQNFFQEFMEAFFPDVAADLDYRRVRFLSQEQFTDFPGGEQKRVDILAETKVKGKDTVILIHVEPQSYYEKPFPERMFRYYMMISLRHRKPVLPIAVFSYEEKTETPDTYTFAFHTIEILRFHYLSIHLMKQNWRNYIRSDNPVAAALLSKMGYTEKERVQVKLEFLRMLARMELDPAKMRLLHGFFDYYLKLNEKEEAEVMENIKMLDPDEAEQVLKLPNSYFDRGYKKGKEEGREEGREEGEERLRRFIVNLLKNQVDVKVIAQASGLSEDEIMKIKRQIEGEKP
>NZ_CP033687.1|WP_110133869.1|2138065_2138365_+|hypothetical-protein
MNPSYDEAEQVLKLPNSYFDRGFKRGKEEGREEGIEIGVEKGREEGREEERKELLQTIPIAIKMLLAGMELQLIVEKTGLSQTEVEKIKQQLETKQDKY
>NZ_CP033687.1|WP_110133870.1|2138835_2140224_+|class-II-fumarate-hydratase
MEYRIEKDTLGEMKVPRDKYWGAQTQRSKENFPIGGEKMPMEVIRAFAHLKKAAAVSNNRLGKLSDAKMKAIVQACEEVMDGKFDEHFPLVVWQTGSGTQSNMNVNEVVARRANEILSGENSAEHVHPNDDVNMSQSSNDTFPTAMHIAAYHELQTRLLPPLEQLKETLLEKEKSYMKIIKIGRTHLQDATPLTLGQEISGWRAMLEKSEHMIKESAKHILNLAIGGTAVGTGINADPTFGDKVAEELEKQTGYPFVSSDNKFHALTSHDEIVHVHGALKGIAADLMKMANDVRWLASGPRSGIGEITIPANEPGSSIMPGKVNPTQCEALTMVAVQVFGNDAAIGFAASQGNFELNVFKPVIIYNFLQSVHLLGDAMKSFDERCVRGIEPNVETIQENVNRSLMLVTALNPHIGYEKAAQIAKLAFKEGTTLKEAAIKTGYVTEEQYEEWIVPEKMVNLNH
>NZ_CP033687.1|WP_014095815.1|2140279_2140486_-|alpha/beta-type-small-acid-soluble-spore-protein
MANNSNSNQLLVSGAEQALDQMKYEIAQEFGVNLGADTTSRANGSVGGEITKRLVQMAEQQLGGTFHS

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Crispr_ID: NZ_CP033687_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_11

2319001-2319139

Orphan

Consensus_repeat	Method
GGAACGGCACAGCAAACGACAATCCGGGGAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_11

>merge|NZ_CP033687|11|2319001-2319139|CRISPRCasFinder
GGACTAGCACAACAAATGAGAATCCGGGGAACGGCACAGCAAACGACAATCCGGGGAACGGCTCCGGTACCGGAAATGGGGCTGGCAACGCGCCGGGGAATGGCTCCGGAACCGGCACAGCAAACGACAATCCGGGGAA

>NZ_CP033687|11|10|2319001-2319139|CRISPRCasFinder
GGACTAGCACAACAAATGAGAATCCGGGGAA	CGGCACAGCAAACGACAATCCGGGGAACGGCTCCGGTACCGGAAATGGGGCTGGCAACGCGCCGGGGAATGGCTCCG
GAACCGGCACAGCAAACGACAATCCGGGGAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_035189578.1\|2331445_2331739_+\|TIGR04197-family-type-VII-secretion-effector	unknown	unknown	gnl\|CDD\|275045
NZ_CP033687.1\|WP_104851333.1\|2314943_2316053_-\|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	unknown	unknown	gnl\|CDD\|180601
NZ_CP033687.1\|WP_013858849.1\|2313633_2314857_+\|acetate-kinase	unknown	unknown	gnl\|CDD\|234680
NZ_CP033687.1\|WP_035181978.1\|2332402_2333392_+\|lactate-dehydrogenase	unknown	unknown	gnl\|CDD\|240661
NZ_CP033687.1\|WP_046721186.1\|2327178_2327868_+\|beta-phosphoglucomutase	unknown	unknown	gnl\|CDD\|213672
NZ_CP033687.1\|WP_110134289.1\|2316280_2316577_+\|WXG100-family-type-VII-secretion-target	unknown	unknown	gnl\|CDD\|227179
NZ_CP033687.1\|WP_110133897.1\|2324673_2326950_+\|glycoside-hydrolase-family-65-protein	unknown	unknown	gnl\|CDD\|237517
NZ_CP033687.1\|WP_017551747.1\|2307287_2308874_+\|gamma-glutamyltransferase	unknown	unknown	gnl\|CDD\|223482
NZ_CP033687.1\|WP_128890942.1\|2320417_2320789_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_061086653.1\|2310522_2310963_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|340863
NZ_CP033687.1\|WP_035181980.1\|2331011_2331194_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_061086652.1\|2308937_2310122_+\|amidase	unknown	unknown	gnl\|CDD\|181375
NZ_CP033687.1\|WP_110133889.1\|2310963_2311353_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|340863
NZ_CP033687.1\|WP_026104646.1\|2305935_2307291_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340877
NZ_CP033687.1\|WP_110133898.1\|2335600_2336782_-\|AGE-family-epimerase/isomerase	unknown	unknown	gnl\|CDD\|225493
NZ_CP033687.1\|WP_110133891.1\|2321233_2322643_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP033687.1\|WP_110133896.1\|2323241_2324648_+\|SLC45-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340871
NZ_CP033687.1\|WP_110133888.1\|2305170_2305647_-\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224439
NZ_CP033687.1\|WP_110133890.1\|2312430_2313309_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378400
NZ_CP033687.1\|WP_014095657.1\|2334050_2335469_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340924

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_035189578.1\|2331445_2331739_+\|TIGR04197-family-type-VII-secretion-effector	gnl\|CDD\|275045	TIGR04197, conserved_hypothetical_protein, type VII secretion effector, SACOL2603 family. Members of this protein family are similar in length and sequence (although remotely) to the WXG100 family of type VII secretion system (T7SS) targets, described by family TIGR03930. Phylogenetic profiling shows that members of this family are similarly restricted to species with T7SS, marking this family as a related set of T7SS effectors. Members include SACOL2603 from Staphylococcus aureus subsp. aureus COL. Oddly, members of family pfam10824 (DUF2580), which appears also to be related, seem not to be tied to T7SS.	3.27538e-12
NZ_CP033687.1\|WP_104851333.1\|2314943_2316053_-\|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	gnl\|CDD\|180601	PRK06520, PRK06520, 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase.	0
NZ_CP033687.1\|WP_013858849.1\|2313633_2314857_+\|acetate-kinase	gnl\|CDD\|234680	PRK00180, PRK00180, acetate kinase A/propionate kinase 2; Reviewed.	0
NZ_CP033687.1\|WP_035181978.1\|2332402_2333392_+\|lactate-dehydrogenase	gnl\|CDD\|240661	cd12185, HGDH_LDH_like, Putative Lactate dehydrogenase and (R)-2-Hydroxyglutarate Dehydrogenase-like proteins, NAD-binding and catalytic domains. This group contains various putative dehydrogenases related to D-lactate dehydrogenase (LDH), (R)-2-hydroxyglutarate dehydrogenase (HGDH), and related enzymes, members of the 2-hydroxyacid dehydrogenases family. LDH catalyzes the interconversion of pyruvate and lactate, and HGDH catalyzes the NAD-dependent reduction of 2-oxoglutarate to (R)-2-hydroxyglutarate. Despite often low sequence identity within this 2-hydroxyacid dehydrogenase family, these proteins typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann fold NAD+ binding form. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain.	2.4888e-179
NZ_CP033687.1\|WP_046721186.1\|2327178_2327868_+\|beta-phosphoglucomutase	gnl\|CDD\|213672	TIGR01990, bPGM, beta-phosphoglucomutase. This model represents the beta-phosphoglucomutase enzyme which catalyzes the interconverison of beta-D-glucose-1-phosphate and beta-D-glucose-6-phosphate. The 6-phosphate is capable of non-enzymatic anomerization (alpha <-> beta) while the 1-phosphate is not. A separate enzyme is responsible for the isomerization of the alpha anomers. Beta-D-glucose-1-phosphate results from the phosphorylysis of maltose (2.4.1.8), trehalose (2.4.1.64) or trehalose-6-phosphate (2.4.1.216). Alternatively, these reactions can be run in the synthetic direction to create the disaccharides. All sequenced genomes which contain a member of this family also appear to contain at least one putative maltose or trehalose phosphorylase. Three species, Lactococcus, Enterococcus and Neisseria appear to contain a pair of paralogous beta-PGM's. Beta-phosphoglucomutase is a member of the haloacid dehalogenase superfamily of hydrolase enzymes. These enzymes are characterized by a series of three catalytic motifs positioned within an alpha-beta (Rossman) fold. beta-PGM contains an inserted alpha helical domain in between the first and second conserved motifs and thus is a member of subfamily IA of the superfamily. The third catalytic motif comes in three variants, the third of which, containing a conserved DD or ED, is the only one found here as well as in several other related enzymes (TIGR01509). The enzyme from L. lactis has been extensively characterized including a remarkable crystal structure which traps the pentacoordinate transition state. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	1.63904e-83
NZ_CP033687.1\|WP_110134289.1\|2316280_2316577_+\|WXG100-family-type-VII-secretion-target	gnl\|CDD\|227179	COG4842, COG4842, Uncharacterized protein conserved in bacteria [Function unknown].	6.33391e-22
NZ_CP033687.1\|WP_110133897.1\|2324673_2326950_+\|glycoside-hydrolase-family-65-protein	gnl\|CDD\|237517	PRK13807, PRK13807, maltose phosphorylase; Provisional.	0
NZ_CP033687.1\|WP_017551747.1\|2307287_2308874_+\|gamma-glutamyltransferase	gnl\|CDD\|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP033687.1\|WP_061086653.1\|2310522_2310963_+\|hypothetical-protein	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.	5.77463e-21
NZ_CP033687.1\|WP_014095657.1\|2334050_2335469_+\|MFS-transporter	gnl\|CDD\|340924	cd17366, MFS_ProP, Proline/betaine transporter of the Major Facilitator Superfamily of transporters. This subfamily is composed of Escherichia coli proline/betaine transporter, also called proline porter II (PPII), and similar proteins. ProP is a proton symporter that senses osmotic shifts and responds by importing osmolytes such as proline, glycine betaine, stachydrine, pipecolic acid, ectoine and taurine. It is both an osmosensor and an osmoregulator which is available to participate early in the bacterial osmoregulatory response. The ProP subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	6.8387e-178
NZ_CP033687.1\|WP_061086652.1\|2308937_2310122_+\|amidase	gnl\|CDD\|181375	PRK08310, PRK08310, amidase; Provisional.	5.71802e-161
NZ_CP033687.1\|WP_110133889.1\|2310963_2311353_+\|hypothetical-protein	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.	3.85652e-15
NZ_CP033687.1\|WP_026104646.1\|2305935_2307291_+\|MFS-transporter	gnl\|CDD\|340877	cd17319, MFS_ExuT_GudP_like, Hexuronate transporter, Glucarate transporter, and similar transporters of the Major Facilitator Superfamily. This family is composed of predominantly bacterial transporters for hexuronate (ExuT), glucarate (GudP), galactarate (GarP), and galactonate (DgoT). They mediate the uptake of these compounds into the cell. They belong to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.06165e-55
NZ_CP033687.1\|WP_110133898.1\|2335600_2336782_-\|AGE-family-epimerase/isomerase	gnl\|CDD\|225493	COG2942, COG2942, N-acyl-D-glucosamine 2-epimerase [Carbohydrate transport and metabolism].	1.21679e-101
NZ_CP033687.1\|WP_110133891.1\|2321233_2322643_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	3.57474e-169
NZ_CP033687.1\|WP_110133896.1\|2323241_2324648_+\|SLC45-family-MFS-transporter	gnl\|CDD\|340871	cd17313, MFS_SLC45_SUC, Solute carrier family 45 and similar sugar transporters of the Major Facilitator Superfamily of transporters. This group includes the solute carrier 45 (SLC45) family as well as plant sucrose transporters (SUCs or SUTs) and similar proteins such as Schizosaccharomyces pombe general alpha-glucoside permease. the SLC45 family is composed of four (A1-A4) vertebrate proteins as well as related insect proteins such as Drosophila sucrose transporter SCRT or Slc45-1. Members of this group transport sucrose and other sugars like maltose into the cell, with the concomitant uptake of protons (symport system). Plant sucrose transporters are crucial to carbon partitioning, playing a key role in phloem loading/unloading. They play a key role in loading and unloading of sucrose into the phloem and as a result, they control sucrose distribution throughout the whole plant and drive the osmotic flow system in the phloem. They also play a role in the exchange of sucrose between beneficial symbionts (mycorrhiza and Rhizobium) as well as pathogens such as nematodes and parasitic fungi. There are nine sucrose transporter genes in Arabidopsis and five in rice. Vertebrate SLC45 family proteins have been implicated in the regulation of glucose homoeostasis in the brain (SLC45A1), with skin and hair pigmentation (SLC45A2), and with prostate cancer and myelination (SLC45A3). Mutations in SLC45A2, also called MATP (membrane-associated transporter protein) or melanoma antigen AIM1, cause oculocutaneous albinism type 4 (OCA4), an autosomal recessive disorder of melanin biosynthesis that results in congenital hypopigmentation of ocular and cutaneous tissues. The SLC45 family and related sugar transporters belong to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	5.41368e-105
NZ_CP033687.1\|WP_110133888.1\|2305170_2305647_-\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	5.04196e-37
NZ_CP033687.1\|WP_110133890.1\|2312430_2313309_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378400	pfam10114, PocR, Sensory domain found in PocR. PocR, a ligand binding domain, has a novel variant of the PAS-like Fold. Evidence suggests that it binds small hydrocarbon derivatives such as 1,3-propanediol. In (Natural history of sensor domains in bacterial signaling systems by Aravind L, LM Iyer, Anantharaman V, from 'Sensory Mechanisms in Bacteria: Molecular Aspects of Signal Recognition.' Caister Academic Press. 2010) - see (http://de.scribd.com/doc/28576661/Bacterial-Signaling-Chapter).	1.22866e-46

>NZ_CP033687.1|WP_110134289.1|2316280_2316577_+|WXG100-family-type-VII-secretion-target
MAGQIRMTPEELKAKAQRYDNAGQLIEQLLRDLTNLQNELRGEWEGRAFQGFDDQFNQLKPKVQNFAQLMHDINTQLNKTADAVAQHDEELSRNFGLQ
>NZ_CP033687.1|WP_104851333.1|2314943_2316053_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase
MQLARKTTPPFRADHVGSMLRPEKLKQARRRQESGEIPKEALRELENEEIKRIVEKQKEIGLQSVTDGEFRRAYWHFDFLENLTGVQGYESGGGIQFKEKQTKSHSIRIIGDLDFSGHPMIDDYKFLHSIAGDHMPKMTIPSPSMLHFRGKIAYGRYQADEDLFFHDLGKAYKKAIAAFYDAGCRYLQLDDTAWAYLCSDEQKEQLKARGLNPDHLEKLYARTINEAVSGRPEDLTVTMHICRGNFRSTWIASGGYEPVAETLFNGLNIDGFFLEYDSDRAGGFEPLRHVQRKDLQIVLGLVTSKFGELENADDVKRRIDEASKYVPLEQLCLSPQCGFASTEEGNLLTEEEQWAKLSHVVKIAGEVWG
>NZ_CP033687.1|WP_013858849.1|2313633_2314857_+|acetate-kinase
MKKIMAINAGSSSLKFKVFNMPDESILIGGVFERIGFDAPEVSYKINGFRQKEKPPIHDHRDAADYLIEILLKNHIVDDLNEISAVGHRITHGGSDFSDSAVLDRIVIQKIENLCELAPLHNPAGLLGIRTFMKRLPKACAVAVFDTSFHQTLAPETYLYPVPLKLYNEYHIRKYGFHGTNHQYVANEAALLLEKPLKDLKIISCHLGNGSSICAIQGGKSVNTSMGFTPLAGLMMGTRSGTVDPSIIPFIMKKTGQTIDEVMDMFNKESGLLGISGISNDFRDVELAAKAHNEQAELAIKMFVNRVTECVGGYVALMGGVDAIVFTAGIGEHSASVRQAVVSNLAYLGAKLDFRSNEENGPYIHTPDSKVSLLVIPANEELMIARDTWRLSEGQAARLSEKQTVRV
>NZ_CP033687.1|WP_110133890.1|2312430_2313309_-|helix-turn-helix-domain-containing-protein
MENKQQIEKVMEMFSSATGLTAVYVDIDGKEISDDDQFPPVCQIIRQVPHLRKHCQTCAKFGGFETMKNGQPCMYRCHAGLADFAVPVKSRENTLYGFIIGGQVRLEDDETQVKDFLQQQPLDLSSHRDFAAAYSKLPVFSLEKLSASAEVLGTLSEYYLSSVLNEEAKPAKESTAQVKKHASSKKEIKQALQYIQKHIHQPVTLEEVAGHVYLSPYYFSKLFKKETGETFVSFVNRQKMNLAKDMLANDDLPVSYIAHSLGFREISYFSKVFKRYYQTTPTSYRAMSRKKG
>NZ_CP033687.1|WP_110133889.1|2310963_2311353_+|hypothetical-protein
MVFKIASILAPTFAGIAIIKLQFNQFIILNSITFLIAALFTLSIKYENKNQTIQKKASPFDHLKSGLKYFWGNKIVFWSVVLISFANIAVGSYNVNLVNMIQNDLNLSANVYGVVLTFYSVGSFLINLY
>NZ_CP033687.1|WP_061086653.1|2310522_2310963_+|hypothetical-protein
MVKVRSLFSKNHSVFFLWTGQGIFSIGSIVYSMALSWYVINETKSPFVMGTVLLVGLLPRIVFSIISGVFGDRISKKKFILSIDLLRFIIRFVWGVSLFYHAFNIVEVYIYTFVLSLIDAVFNPIYNAILPEVANTDDLSRLVSIN
>NZ_CP033687.1|WP_061086652.1|2308937_2310122_+|amidase
MEDKWNAFIDPDVTVWPKRNGLLDGYTFAVKDVFAVKGHRNAAGNPDWYDFHPEAGENAPVIEWLLNEGARLTGMTHTDELMYSLNGENFHYGTPVNPVLKDRIPGGSSSGSAVAAAAGCTDFAIGTDTGGSVRIPSAYCGIFGFRPSHGVIKMEGVIPLAPSFDTIGWMSKDPGILYKVGQVLFKPEKDIRPQFESIFFAEDAWELAGEETRKLLESKWHHLLKNRKQHVVRTAIADQALKSWSHTFRLLQGREVWKTHGAWIEKARPKFGPDIAERFKWASTIVEDSHWEKANQLRLNIRDKLRGLLGSSGLLVLPTTPGPAPATGRSMEEIEKTREHTMQLSCIAGLAGLPQLTIPFLTATGEPIGLSVVAGYRQDLKLLAWVEELMLSAA
>NZ_CP033687.1|WP_017551747.1|2307287_2308874_+|gamma-glutamyltransferase
MKLNDPKIGTKTMIVSPHYLASAAGARILEKGGNAFDAAVAVSACLAVVYPHMTGLGGDSFWLTWHHSDRVIRAYNGSGRSGYCVTRENYANEDKIPLRGARSAITVPGMADSWDAILKEYGKFTLKEVLEPAIEYAWNGFPLSPDQYKNTVMARAILMKTKRTSDIYLPNGKVPQIGQKFVQKELGRTLMKIAEKGRDVFYKGPIAKEIVAAMKADGGYLLVDDFADHYGNWTDPIFTHYHDYQIYQAPPNSQGFSALMALNILENFDFTLIEHGSYEYYHILIETLKKVFQDRNEVLTDPEFSPVPLEKLLSKTYAAKLAEEINWDRAMEYNAEPLGRDTAYAAVVDDEGNAVSFIQSLYFEFGSAFVAGSTGILMQNRGSFFSLDAGHVNTLEPHKRTFHTLMPAMAFLDGKPSILYGTQGGEGQPQTQTALITRVVHYGMNPQQAVSAPRWVWGRTWGEPTEELKVEERVGSEVCNALSKAGHVVRKVSAYDGVMGHAHMIQINEHGFRIGGTDPRCDGAAIGW
>NZ_CP033687.1|WP_026104646.1|2305935_2307291_+|MFS-transporter
MFNNIIRNKKKHNEIYVRKHYNTKEKGEAVHLKKRHPVVYVVLFALGWAFMYADRNILSPVMGVIQDDWGLSKSELGLMSTIFFLAYAAMQIPAGFLADRIGRVKVLVSGYILFGVGTIMSGMAPGLLAFLMIRFVTGLGEGTYYGPQYAISSVAISQKYRGISSALINSGMAVGISLGFIASSYFTFTLKKDWQFSFYVFGILTVLVAILMGLLIKDPHRRSRIKPTGTGVTEPENVRELFSKNHLITYVLIFCSLYGFFSMMTWLPYYLQTERGVPGSQTGVIASLVPWSSIPGALFFGYLSDKIKNKKIMVFTLAVLGTICQFIVPYSDSFSFMIAGLVVYGLIGKLALDPVLISFIADHTSSAMYARVFGIFNFAGMLSSIFAPYITGYLAEVTGNMEIGFYLSGILLLFGGFLFLFSDGQPFKAAVKKQRRTQRYEAKFVPGRENP
>NZ_CP033687.1|WP_110133888.1|2305170_2305647_-|Lrp/AsnC-family-transcriptional-regulator
MPRQYDGAAVQLDEIDRQIIQLLNGNGRVSFTDLAKEIKLSRVAVQSRVHSLVENGVIECFTAVVNPEKIGLHQSAFFNVEVEPKHLQEVAEILAKDPAVSSLYHMSGPSKLHMHGLFKDNEEMELFLKERLYPLPGIMSVDCQILLKRYKSRIGMKL
>NZ_CP033687.1|WP_128890942.1|2320417_2320789_+|hypothetical-protein
MPWIGLSVAISFSMVAVAVYLLRQLKMVGMFLLLMVLCLYLFLTDTLGIHFDPASAAAMWQRVSPLQYIQNLLAGFDSHNVDSVRYLIVLVSVGLLAEIGQLFVLNRFTKAGEAEDDDVHQAL
>NZ_CP033687.1|WP_110133891.1|2321233_2322643_+|group-II-intron-reverse-transcriptase/maturase
MKVTEETNKCRKQEETCCQKDTAEQEGYGRGHSFKRITENNTTNTNRQKEWMLERILSSNNLHRAYKKVKKNKGAGGVDGMKTGELLAYLTEHQRELVLSIRNGTYKPQPVRRVEIPKDNGKTRKLGIPTVVDRVIQQAISQVLVPIYERKFSDNSYGFRPHRSTHQALLKCQKNVNEGYQYVVDLDLEQYFDTVNHSKLIQILSETIHDGRVISLIHKFLNAGVMIKGIRTTNDFGVPQGGPLSPLLANVMLNELDKEMDARNHRFVRYADDVIIFCKSRRSCERTYHNILPFIEKKLRLKVNREKTTITHIRNIKFLSYGFYLYEGKCKFRVHPKGVQKLKEKIRRITGRSNGLSVEERKKRLNDTVRGWVNYYKLADMKSLVTRLDQWTRRRMRMVTWKRWKRVRTRFYWLKKLGINKRKAWEWANTRKGYWRISGSHILARTLTNELFRRARYISFLDYYLSVRS
>NZ_CP033687.1|WP_110133896.1|2323241_2324648_+|SLC45-family-MFS-transporter
MRAMVNTDEKSIGRVKSSATVKDGKKIDSHQLPALPISTIWMISFGFLGVQMAFSLQSSNMGRIFQTIGADPTKLGFFFILPPLAGLVVQPLVGYFSDRTWIPKLGRRIPYLLVGAAVAVIVMCLLPNAGSFGFGFGSITALTFGAVTILFMDLSSNVAMQPFKMMVGDMVNEEQKGFAYAVQSFLSNSGAVLACIFPFVLTALGVSNSAPKGVVPQSVVVSFYSGAVILIVCSLFTVFKVKEYSPDEYAVYHGIQNQAQKEKMGMFQLLLNAPKEFWMITVVQFFCWMGFQYLWTYGAGAVAKNAWNAVDPSSTAYQEAANWFGVLSGVYSLAAVFWSLVLTKVPKNKQKPAYAFSLVLGGVGFGSVFFIHNPGTLLVSFILIGIAWAAMMAFPFTILTNALSGENMGTYLGLFNGSICLPQIVASCLSFLIFPALGSSMPAMILLSGVLLVIGAASVSLIKKTQTK
>NZ_CP033687.1|WP_110133897.1|2324673_2326950_+|glycoside-hydrolase-family-65-protein
MKRIFEVQPWNVVSHDFNRAEKRLQESMTSLGNGYMGMRGFFEENYSGDTLKGIYLGGVWFPDRTRVGWWKIGYPEYFGKVINAINFIKINIALNGEFIDLAKDEITGFELNLDMKNARLTRSFTVEKGTVKVVVTFERFLSVAQKELSVQRVRLKNLGSDDVDVKIISAIDAEVKNEDANYGERFWEVLQTDQKEQSGSLVAITKANPFGTPRFTVGAEMHHRTALQAKVAAPAHDKEVVNGFSGKLVAGSEIDFEKRVIVVTSRDYHTQNNLVSAMNAISEKTDNLSYDELFDAHRAIWAERWEKSDVKIEGDVAAQQGIRFNLFQMFSTYYGEDARLNIGPKGFTGEKYGGATYWDTEAFALPFYLGVAEPKISKNLLKYRYQQLDGAYHNAKKQGLKGALFPMVTFDGIESHNEWEITFEEIHRNGDIAFAIYNYTRYTGDKSYVLNEGSKVLTEISRFWADRVHFSKRKQKYMLHGVTGPDEYENNVDNNWYTNYMARWTLAYTLQVLEEVSQEQAAVLNVTEEEKQLWQDIVDRMYLPEDEELGIFVQHDGFLDKDIKPVSEIPADELPINQHWSWDKILRSAYIKQADVLQGIWNFIDEFTPEQKKRNFDFYEPLTVHESSLSASIHAILASDLHDENKAVEMYERTSRLDLDNYNNDTEDGLHITSMTGSWLAIVQGFAGMRVRDGKLHFAPFLPKKWDKYQFRLLFRGRLIEVGVDTNGVSLELLEGEPLTVGLYGKDVELVAQSSVFV
>NZ_CP033687.1|WP_046721186.1|2327178_2327868_+|beta-phosphoglucomutase
MRSFHDIKGFAFDLDGVLTDTARFHAQAWKKTAEEVGTKWTDELAAGLKGISRMDSLEMILKAGNCEHSYTHEQKAQLADEKNEYYKKLIDTLTPEDILPGMAEFLMEVKHKGYKLAVASASKNAPIILERLGIADMFDAVVDPAALKSGKPDPEIFVRAAELMNLQPCEVIGLEDSIAGIKSINGAGEVSVGIGDKDELYEAAIHFASTVEVSLSTIQGDPYFSKSNL
>NZ_CP033687.1|WP_035181980.1|2331011_2331194_+|hypothetical-protein
MDEMVHTLMNQKSRLSSQKIHIQQDLADINAKIKRLKSALGELEKEISNLQDKAKPILNF
>NZ_CP033687.1|WP_035189578.1|2331445_2331739_+|TIGR04197-family-type-VII-secretion-effector
MGEIKLNVELFNSNIEQLQAAVSDMETNLIKTTSFDQTNINPFKEELKQVTKAMELLSKYKSILEADIQTLKNTGEAIKKLDEQIEKSYDNYRNLQQ
>NZ_CP033687.1|WP_035181978.1|2332402_2333392_+|lactate-dehydrogenase
MRKVVAYETRADEFPLFQKFARKFDLDIKYVDDVLTPETAVEAKGAEAVTILGNYPVGAETFMALRDAGVKYIGLRTAGYNHIDQEAAKAYGIRFSNVAYSPYCVADFATMLILMCVRKAKQILSRVEAQDFSVEGIQGREMHNLTIGIIGAGRIGSIVAKNLSGFGCNIIAHDTVERDELRGILKYVSLDELLKESDVITIHTPLFDRTYHMINQDRIAKMKDGVCIINCSRGAVVDTDALIAGIEAGKVGAAGIDVLEDEEGIFHYDRRTDILAHHQLAILRSFPNVIVTPHTAFYTDQAVSDMVEMALTSLVSFMETGKSRWEIKS
>NZ_CP033687.1|WP_014095657.1|2334050_2335469_+|MFS-transporter
MVFNKKKINIVNIRQTKKSVFATGVGNAMEWFDFGLYSYLAVIISRNFFSAVENDELKLMFTFATFAIAFLMRPLGGVIFGRIGDKYGRKVVLTITIILMAFSTLLIGLLPTYDQIGIWAPVLLLVARIIQGFSTGGEYAGAMVYIAESSPDNKRNVLGSGLEIGTLAGYILASLLASTLFITLTDQQMATWGWRIPFLLGLPLGLVGFYLRAHLEETPIFENELSVEGVQEESFLSILKNHKKDILVCFVSVAFFNVTNYMLLSYMPSYLDEVIGLSSTAGTVLITLIMVIMVPLALLFGKLSDQIGNKTVLIMGLGGLTLLSVLAFYFIHLNTIAFVFLGILILGILLSTYEGTMPGTLPTMFYTDIRYRTLAVTFNVSVSLFGGTTPLISTWLVHQTGNALAPAFYLTFFSLIGFFVILFLFTSTSGKSLKGSYPTVATKTEYKEAIENPRHSLWWLMEKQEENKRLYN
>NZ_CP033687.1|WP_110133898.1|2335600_2336782_-|AGE-family-epimerase/isomerase
MDFKDPHVLKQQIIQILEFYYPACIDTENGGYINGFLDNGSINDRETKHLVGTSRFIYNFSIGSLIGGPEWCAQAAAHGIEFLKNHHRDKKYGGYFFELKGQIVKDPAKMAYGHAFALLAAAIADQAGIRGAKELIEDLYHVTEQHFWDPDDGLYRDEWDSSWSTLSSYRGQNANMHMCEAMLTAYEATGEKKYLNRAYKLAESVCRTLKERSGGMIWENYTPDWQPDWTYHLHQTKDEFRPYGFIPGHQLEWSKLLMWLDRHLSEPWIVETAEELYGKAWEKGADETFGGIFFALSPQGEVIDTDKNYWVISEAIAASALLAAKTGKSIYSERYNQLFSYASNYLIDHQYGGWYKLLNRKNERLPGPKSASPKTDYHPVAACYQALQAFSKP

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Crispr_ID: NZ_CP033687_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_12

2469529-2469978

Orphan

Consensus_repeat	Method
AANTGTCNTTTTGNAGCNGNCAAAAGGACAAAA	CRT
TTTTGAAGCTGTCAAAAGGACAAAA	CRISPRCasFinder

8 spacers

The CRISPR arrays of NZ_CP033687_12

>merge|NZ_CP033687|12|2469529-2469978|CRT,CRISPRCasFinder
AAGTGTCTTTTTGAAGCTGTCAAAAGGACAAAACAAGCTGTATCTGGGCTCGGAATGTCCTTTTGAAGCTGCCAAAAGGACAAAACACGTTGCATCCGGTCCCGAAATGTCCTTTTGAAGCAGTCAAAAGGACAAAACGCGTTGCATCGGGGTCCAAAATGTCTTTTTGAAGCTGTCAAAAGGACAAAACAAGCTGTATCTGGGCTCGGAATGTCCTTTTGAAGCTGCCAAAAGGACAAAAGGAGCCGTGAACTGAAACAAAATGTCCTTTTGAAGCTGTCAAAAGGACAAAAGGAGCCGTGGACCGGAGCAAATTGTTCTTTTGGAGCATCCAAAAGGACAAAAGGAGCCATTGACCGGAACAAAATGTCTTTTTGGAGTGTTCAAAAGGACAAAAATAACCGGGGAACAGAGCATATTTGGTCTTTTTGAAGTGTCAAAATACCAAAT

>NZ_CP033687|12|4|2469529-2469978|CRT
AAGTGTCTTTTTGAAGCTGTCAAAAGGACAAAA	CAAGCTGTATCTGGGCTCG
GAATGTCCTTTTGAAGCTGCCAAAAGGACAAAA	CACGTTGCATCCGGTCCCG
AAATGTCCTTTTGAAGCAGTCAAAAGGACAAAA	CGCGTTGCATCGGGGTCCA
AAATGTCTTTTTGAAGCTGTCAAAAGGACAAAA	CAAGCTGTATCTGGGCTCG
GAATGTCCTTTTGAAGCTGCCAAAAGGACAAAA	GGAGCCGTGAACTGAAACA
AAATGTCCTTTTGAAGCTGTCAAAAGGACAAAA	GGAGCCGTGGACCGGAGCA
AATTGTTCTTTTGGAGCATCCAAAAGGACAAAA	GGAGCCATTGACCGGAACA
AAATGTCTTTTTGGAGTGTTCAAAAGGACAAAA	ATAACCGGGGAACAGAGCAT
ATTTGGTCTTTTTGAAGTGTCAAAATACCAAAT

>NZ_CP033687|12|11|2469537-2469978|CRISPRCasFinder
TTTTGAAGCTGTCAAAAGGACAAAA	CAAGCTGTATCTGGGCTCGGAATGTCC
TTTTGAAGCTGCCAAAAGGACAAAA	CACGTTGCATCCGGTCCCGAAATGTCC
TTTTGAAGCAGTCAAAAGGACAAAA	CGCGTTGCATCGGGGTCCAAAATGTCT
TTTTGAAGCTGTCAAAAGGACAAAA	CAAGCTGTATCTGGGCTCGGAATGTCC
TTTTGAAGCTGCCAAAAGGACAAAA	GGAGCCGTGAACTGAAACAAAATGTCC
TTTTGAAGCTGTCAAAAGGACAAAA	GGAGCCGTGGACCGGAGCAAATTGTTC
TTTTGGAGCATCCAAAAGGACAAAA	GGAGCCATTGACCGGAACAAAATGTCT
TTTTGGAGTGTTCAAAAGGACAAAA	ATAACCGGGGAACAGAGCATATTTGGTC
TTTTTGAAGTGTCAAAATACCAAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_110133921.1\|2461161_2464362_+\|carbamoyl-phosphate-synthase-large-subunit	unknown	unknown	gnl\|CDD\|235393
NZ_CP033687.1\|WP_014095526.1\|2476981_2477185_+\|iron-containing-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|182595
NZ_CP033687.1\|WP_071451855.1\|2466314_2467022_+\|orotidine-5'-phosphate-decarboxylase	unknown	unknown	gnl\|CDD\|234695
NZ_CP033687.1\|WP_110133926.1\|2479958_2481473_-\|multidrug-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP033687.1\|WP_014095525.1\|2477287_2477710_+\|methylglyoxal-synthase	unknown	unknown	gnl\|CDD\|179969
NZ_CP033687.1\|WP_046721302.1\|2460080_2461178_+\|glutamine-hydrolyzing-carbamoyl-phosphate-synthase-small-subunit	unknown	unknown	gnl\|CDD\|237139
NZ_CP033687.1\|WP_046720824.1\|2477873_2478449_+\|5-formyltetrahydrofolate-cyclo-ligase	unknown	unknown	gnl\|CDD\|274270
NZ_CP033687.1\|WP_014095536.1\|2464358_2465135_+\|dihydroorotate-dehydrogenase-electron-transfer-subunit	unknown	unknown	gnl\|CDD\|99814
NZ_CP033687.1\|WP_061565658.1\|2457838_2458738_+\|aspartate-carbamoyltransferase-catalytic-subunit	unknown	unknown	gnl\|CDD\|234849
NZ_CP033687.1\|WP_035189240.1\|2457065_2457608_+\|bifunctional-pyr-operon-transcriptional-regulator/uracil-phosphoribosyltransferase-PyrR	unknown	unknown	gnl\|CDD\|235365
NZ_CP033687.1\|WP_110134292.1\|2458797_2460084_+\|dihydroorotase	unknown	unknown	gnl\|CDD\|236479
NZ_CP033687.1\|WP_019721982.1\|2476141_2476978_+\|rhamnulose-1-phosphate-aldolase	unknown	unknown	gnl\|CDD\|131673
NZ_CP033687.1\|WP_110133925.1\|2473381_2474842_+\|rhamnulokinase	unknown	unknown	gnl\|CDD\|198349
NZ_CP033687.1\|WP_071451856.1\|2467021_2467657_+\|orotate-phosphoribosyltransferase	unknown	unknown	gnl\|CDD\|234771
NZ_CP033687.1\|WP_110133924.1\|2471018_2472128_+\|transposase	unknown	unknown	unknown
NZ_CP033687.1\|WP_110133923.1\|2470024_2470930_-\|NERD-domain-containing-protein	unknown	unknown	gnl\|CDD\|377990
NZ_CP033687.1\|WP_110134293.1\|2465332_2466322_+\|dihydroorotate-dehydrogenase	unknown	unknown	gnl\|CDD\|235982
NZ_CP033687.1\|WP_019721979.1\|2472311_2473172_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP033687.1\|WP_017551449.1\|2468231_2469407_-\|IS256-family-transposase	unknown	unknown	gnl\|CDD\|307151
NZ_CP033687.1\|WP_061564830.1\|2478445_2479786_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_110133921.1\|2461161_2464362_+\|carbamoyl-phosphate-synthase-large-subunit	gnl\|CDD\|235393	PRK05294, carB, carbamoyl-phosphate synthase large subunit.	0
NZ_CP033687.1\|WP_014095526.1\|2476981_2477185_+\|iron-containing-alcohol-dehydrogenase	gnl\|CDD\|182595	PRK10624, PRK10624, L-1,2-propanediol oxidoreductase; Provisional.	2.7739e-23
NZ_CP033687.1\|WP_071451855.1\|2466314_2467022_+\|orotidine-5'-phosphate-decarboxylase	gnl\|CDD\|234695	PRK00230, PRK00230, orotidine-5'-phosphate decarboxylase.	1.0178e-122
NZ_CP033687.1\|WP_110133926.1\|2479958_2481473_-\|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].	4.80839e-73
NZ_CP033687.1\|WP_014095525.1\|2477287_2477710_+\|methylglyoxal-synthase	gnl\|CDD\|179969	PRK05234, mgsA, methylglyoxal synthase; Validated.	1.085e-77
NZ_CP033687.1\|WP_046721302.1\|2460080_2461178_+\|glutamine-hydrolyzing-carbamoyl-phosphate-synthase-small-subunit	gnl\|CDD\|237139	PRK12564, PRK12564, carbamoyl-phosphate synthase small subunit.	0
NZ_CP033687.1\|WP_046720824.1\|2477873_2478449_+\|5-formyltetrahydrofolate-cyclo-ligase	gnl\|CDD\|274270	TIGR02727, Uncharacterized_protein_YqgN, 5,10-methenyltetrahydrofolate synthetase. This enzyme, 5,10-methenyltetrahydrofolate synthetase, is also called 5-formyltetrahydrofolate cycloligase. Function of bacterial proteins in this family was inferred originally from the known activity of eukaryotic homologs. Recently, activity was shown explicitly for the member from Mycoplasma pneumonia. Members of this family from alpha- and gamma-proteobacteria, designated ygfA, are often found in an operon with 6S structural RNA, and show a similar pattern of high expression during stationary phase. The function may be to deplete folate to slow 1-carbon biosynthetic metabolism. [Central intermediary metabolism, One-carbon metabolism].	3.82633e-60
NZ_CP033687.1\|WP_014095536.1\|2464358_2465135_+\|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.	3.12569e-117
NZ_CP033687.1\|WP_061565658.1\|2457838_2458738_+\|aspartate-carbamoyltransferase-catalytic-subunit	gnl\|CDD\|234849	PRK00856, pyrB, aspartate carbamoyltransferase catalytic subunit.	9.56467e-152
NZ_CP033687.1\|WP_035189240.1\|2457065_2457608_+\|bifunctional-pyr-operon-transcriptional-regulator/uracil-phosphoribosyltransferase-PyrR	gnl\|CDD\|235365	PRK05205, PRK05205, bifunctional pyr operon transcriptional regulator/uracil phosphoribosyltransferase PyrR.	1.6155e-101
NZ_CP033687.1\|WP_110134292.1\|2458797_2460084_+\|dihydroorotase	gnl\|CDD\|236479	PRK09357, pyrC, dihydroorotase; Validated.	0
NZ_CP033687.1\|WP_019721982.1\|2476141_2476978_+\|rhamnulose-1-phosphate-aldolase	gnl\|CDD\|131673	TIGR02624, Rhamnulose-1-phosphate_aldolase, rhamnulose-1-phosphate aldolase. Members of this family are the enzyme RhaD, rhamnulose-1-phosphate aldolase.	0
NZ_CP033687.1\|WP_110133925.1\|2473381_2474842_+\|rhamnulokinase	gnl\|CDD\|198349	cd07771, FGGY_RhuK, L-rhamnulose kinases; a subfamily of the FGGY family of carbohydrate kinases. This subfamily is predominantly composed of bacterial L-rhamnulose kinases (RhuK, also known as rhamnulokinase; EC 2.7.1.5), which are encoded by the rhaB gene and catalyze the ATP-dependent phosphorylation of L-rhamnulose to produce L-rhamnulose-1-phosphate and ADP. Some uncharacterized homologous sequences are also included in this subfamily. The prototypical member of this subfamily is Escherichia coli RhuK, which exists as a monomer composed of two large domains. The ATP binding site is located in the cleft between the two domains. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of divalent Mg2+ or Mn2+ is required for catalysis. Although an intramolecular disulfide bridge is present in Rhuk, disulfide formation is not important to the regulation of RhuK enzymatic activity. Members of this subfamily belong to the FGGY family of carbohydrate kinases.	0
NZ_CP033687.1\|WP_071451856.1\|2467021_2467657_+\|orotate-phosphoribosyltransferase	gnl\|CDD\|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	2.58651e-75
NZ_CP033687.1\|WP_110133923.1\|2470024_2470930_-\|NERD-domain-containing-protein	gnl\|CDD\|377990	pfam08378, NERD, Nuclease-related domain. The nuclease-related domain (NERD) is found in a range of bacterial as well as archaeal and plant proteins. It has distant similarity to endonucleases (hence its name) and its predicted secondary structure is helix - sheet - sheet - sheet - sheet - weak sheet/long loop - helix - sheet - sheet. The majority of NERD-containing proteins are single-domain, but in several cases proteins containing NERD have additional domains which in 75% of cases are involved in DNA processing.	5.43509e-21
NZ_CP033687.1\|WP_110134293.1\|2465332_2466322_+\|dihydroorotate-dehydrogenase	gnl\|CDD\|235982	PRK07259, PRK07259, dihydroorotate dehydrogenase.	0
NZ_CP033687.1\|WP_019721979.1\|2472311_2473172_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	3.28354e-24
NZ_CP033687.1\|WP_017551449.1\|2468231_2469407_-\|IS256-family-transposase	gnl\|CDD\|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	1.32007e-144
NZ_CP033687.1\|WP_061564830.1\|2478445_2479786_+\|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].	3.28718e-51

>NZ_CP033687.1|WP_017551449.1|2468231_2469407_-|IS256-family-transposase
MTHLQFNLNLDVLKEAIMTSDLDAVIKSAVVLVLNEFMEKERDDYLKTSPYERAVERRDYRNGYYERELLMSIGNVTLKVPRTRNGEFSTTLFEKYARCDQAFVLSMLEMVINGVSTRKVTNVVEQLCGKNVSKSFVSSLTQKLDPIVNAWAERPLNTTYYPYVFVDAMYIKVREHHKVISKAVYIATAITEKNTREILGLSVDHAESLESWSSFFKQLKSRGLQSPKLVISDAHMGLQKAIQREFIGTAWQRCNVHFKRNIIEKLPKKDTAEIRVMIKRVFEAVTIEDIRKFKDELINKFGTEARFEKALAILDEGFEDTIQYMNFPENIRMHIRSTNSLERLNQEVRRRERVIRIFPNTQSAFRLVGAVLMQYQDTEYSKRKSLMGKNS
>NZ_CP033687.1|WP_071451856.1|2467021_2467657_+|orotate-phosphoribosyltransferase
MEKYIAGQLLDIEAVFLKPGEPFTWSSGIKSPIYCDNRITLSYPNLRKEIAIGLKKLIEAHFPETEVVAGTATAGIAHAAFVSDLMNLPMVYVRSSAKAHGKGNQIEGRVSTGQKVVVVEDLISTGGSVLTVVHALREAGCEVLGVVSIFTYELPAGAANFAKEGITAYSLSNYSTLLQVGVERGLIREEDLATLEEWRREPEEWGKSKKG
>NZ_CP033687.1|WP_071451855.1|2466314_2467022_+|orotidine-5'-phosphate-decarboxylase
MHKPIIALDFSSEEETLTFLQQFGGEPLYVKVGMELFYQTGPCLIAALKEMGHDIFLDLKLHDIPNTVGRAMKGLARLGVDMVNVHAAGGSDMMKAALAGLEAGTPAGKKRPAILAVTQLTSTSETQMQKEQGILKPLRESVLDYAVLAYDAGLDGVVCSAFEAPDITARLGGAFLKVVPGIRLAGDDVSDQKRVVTPAKARELGSTAIVVGRSITKAPDPYEAYLKVKQQWGNK
>NZ_CP033687.1|WP_110134293.1|2465332_2466322_+|dihydroorotate-dehydrogenase
MECRVPPDSPKDHAERRGIKRRVSPDLRVELPGLSLKNPVMPASGCFGFGREYSHWYDLSELGAIMIKATTTEPRFGNPVPRIAETEAGMLNAIGLQNPGLESVLAEELPFLQSYDVPIIANVAGSTFEDYVYVSARLSKAPNVHALELNISCPNVKSGGIAFGTDPEMAFELTRQVKAVSEVPVYVKLSPNVTDIVAIAKAAEAGGADGLTMINTLLGMKIDLKTSRPLLANETGGLSGPAVKPVAVRMVYEVSREVDIPIIGMGGIMTAEDAVEFLYAGASAVAVGTANFIDPLACPRIIRELPTLMEQLGAESIQDLIGRSHTQHA
>NZ_CP033687.1|WP_014095536.1|2464358_2465135_+|dihydroorotate-dehydrogenase-electron-transfer-subunit
MIQEYMIVKSNRLIAQDIWEMVLAGSLVRQIARPGQFVHVKAGSGFDPLLRRPISIAAVDRKNGALTLLYRVQGKGTRLMANMAPGARLDVLGPLGNGFPVDALRPGQKALLVGGGIGVPPLYELSRQLKAGGVEVRHVLGFESAAHAFYVEKFSTLAPTSVATVDGSWGTKGFVTDVLAAENWAFDCLYACGPAAMLRALEAAYPGQRGFFSLEERMACGTGACYGCVCRPKNDPTGTASKKVCSDGPVFEMGEILI
>NZ_CP033687.1|WP_110133921.1|2461161_2464362_+|carbamoyl-phosphate-synthase-large-subunit
MPKRTDIEKILVIGSGPIVIGQAAEFDYAGTQACLALKEEGYHVVLVNSNPATIMTDTEMADKIYIEPLTPAFVARIIRKERPDALLPTLGGQTGLNIAMELAKSGILDEYGVEVLGTRLGAIEQAEDREAFRELMGKLGEPVPDSMIIHTLEEAYRFIEKAGYPVIVRPAYTLGGTGGGICRNEEELIETVSGGLRQSPVHQCLLEKSIAGFKEIEYEVMRDSEDHAIVVCNMENIDPVGVHTGDSIVVAPSQTLSDKEYQMLRNVSLKIIRALGIEGGCNVQLALDPDSFQYYVIEVNPRVSRSSALASKATGYPIAKLSAKIAVGLTLAEMKNPVTGTSYANFEPALDYVVTKIPRFPFDKFEQAYRRLGTQMKATGEVMAIGRTFEESLLKAVRSLEIGVHHLELEEASGMDVIEKRIKNAGDERLFYIAEALRRGVTIGQLHDWSKIDLFFLHKLENIIRFENTLQEEQWDKEAAWKAKEMGFTDKTIAGLWGTAEEKVYAWRKENGILPVYKMVDTCAGEFASETPYFYGTYEEENESVVTNRKSIIVLGSGPIRIGQGIEFDYATVHAVWAIQEAGYEAIIINNNPETVSTDFSISDKLYFEPLTIEDVMHIIDLEQPEGVVVQFGGQTAINLAEQLANRGVRILGTSLENLDRAEDRDKFDHLLNRLGIKRPLGKTGTSAEEAVRIAAEIGYPVLVRPSFVLGGRAMEIVYHEEDLRQYMKHAVKVSPNQPVLIDRYVTGQEFEVDVIADGRDILIPGIVEHIERAGVHSGDSIAVYPPQRLSEALKAEMVETCRKLASELEIKGLMNIQFIVSHNELFVIEVNPRSSRTVPFLSKITDVPMAKLAMKVILGESLENLGYGTGLRPEKAEVFVKVPVFSFAKLKRVEPTLGPEMKSTGEVMGCDRTFEKALYKGLVAAGMKLSPDGSILFTVADKDKPEALPLAKRFVEIGFTLKATAGTAKFLRENGLAVEEVEKIGGEGATVLDSIQRGDVQFVLNTITKGREYERDGFRIRREAVECGIPCLTSLDTAAAIVSILESISFSIMPMVQGAKQAVHA
>NZ_CP033687.1|WP_046721302.1|2460080_2461178_+|glutamine-hydrolyzing-carbamoyl-phosphate-synthase-small-subunit
MKRQLLLEDGTVFKGEGFGSEKAAYGEIVFTTGMTGYQETLTDPSFYGQIVTFTYPLIGNYGINWNDFEAVKPYVKGVVVKEAASYPSNWRSTLTLDTFLKEKGIPGISGIDTRKLTRKIRAFGTLRAALCAEDEDPEAVIKNLQAKRAIHDAVAQVSTKKRYEMEGPGKHIALVDFGAKKSILTELSKRNCRVTVLPYDTTAADILQLRPDGVMLSNGPGNPKDVACAVDMVKGILGKVPLFGICLGHQLFALACGADTFKLKFGHRGANHPVQDIETGKTVITSQNHGYAVDEHSLAGTDLIVTERALNDGTIEGLAHRKYPAFTVQYHPEASPGPHDSNPLFDKFLTMVEKQKEEQTYAKTH
>NZ_CP033687.1|WP_110134292.1|2458797_2460084_+|dihydroorotase
MDWLIKGGMVLDEKGESVKRDIRIKDGKIAETGSELKEAGEQVYDATGLTVLPGFVDLHVHLREPGFEQKETIRTGTMAAAKGGFTTVAAMPNTKPVTDRPARLLSLKEKISRDAVVRVLPYAAITLDEKGGELVDFAGLKAAGAFAFTDDGVGVQEAGQMLAAMERAKALGMAVVAHCEDNSLIRGGCVHAGSFAAAHGLKGIPSVCESVQIARDVLLAEHTGCHYHVCHISTKESVRVVRDAKRAGIPVTAEVTPHHLLLSEDDIPGPDANWKMNPPLRSKRDRDALIEGLLDGTIDFIATDHAPHTAEEKAKGIEQAPFGITGFETAFPLLYTHFVETGIFTLKQLVDWMTIKPASVFGLPYGTLKTGAPADITAVNLAEEKTIDPDRFLSKGKNTPFLGCVCKGFPQATWGSGKLVWEKELALK
>NZ_CP033687.1|WP_061565658.1|2457838_2458738_+|aspartate-carbamoyltransferase-catalytic-subunit
MQHFLTISGLGNEEILELLEEADAFSKGAVWKAPEPVFAANLFYEPSTRTKCSFEVAERRIGLELLPFEVGASSVQKGETLYDTVKTLQSIGVKVVVIRHQEDEYYRQLAGLALSIVNAGDGSGQHPSQCLLDLLTIKQEFGGFRGLKVCIIGDIVHSRVARSNAEALKKLGATVTCSGPVKWFDPTMHLPYVPVDDGVAEADVVMLLRIQHERHQETAHLTKEAYHRAYGLTVERERIMKPGSIIMHPAPVNRDVEIATSLVECSRSRIFKQMENGVFARMAILKTILQKEKAVFQTA
>NZ_CP033687.1|WP_035189240.1|2457065_2457608_+|bifunctional-pyr-operon-transcriptional-regulator/uracil-phosphoribosyltransferase-PyrR
MAQKAVVMDEIMIRRALTRIAHEIIERNKGIEDTMLIGIKTRGIYLAERLAERIAQIEGRKVEVGELDITLYRDDLSKKTANGEPEVKGANLPSSITDKEIVLVDDVLYTGRTVRAAMDALMDIGRPSRIQLAVLVDRGHRELPIRPDFIGKNIPTSQSERIVVQLTDVDGRDLVTIHDM
>NZ_CP033687.1|WP_110133923.1|2470024_2470930_-|NERD-domain-containing-protein
MLFKERKTSLECALLKSLNNRMKLHEKDIQYLRNLEKGDEGERYFDSLTAALTCDCFVLNDLRLSCNNATFQIDALMITGETIYLFEVKNYEGDFYYERDRIFTKNKSEINNPLLQVKRCESLFRQLILSLGFNMPVSASVVFVNPEFTLYQAPLSAPFIFPNQLKRYMKDLNAISAKLSGKHRRLAEKLSSLHIEESPFLHLPKYEYDQLRKGIVCDACGSFSCAVKGHAMICEDCGHAESVEAAVLRSVREFRMLFPERKITTNDIFDWCRIVESKKRVSRILAKNFNKFRGGRWSYYE
>NZ_CP033687.1|WP_110133924.1|2471018_2472128_+|transposase
MKNLRIEQTNEMILDKFGMGIVEFLISQTHLASRLNSAKSETIKRNPGYSNGDIAKAYIGLLCLGKNKFAEIEPLRSDYDFRPFLKLERVPSPAVLEHRLDEAALSEEWKQIILEESLHLLRKAGAPINPVTIQGKSFIPVDVAMPFAFIGKEGYCLSFGQETSVSGRAAEQLAEGAFLWRLEAKEGSEIAAKLLDLNIDFVMKLQTDASTWVETARKHGTCSSEREGKNVYFGSVAETNTTAGAKKPAYYVFKLIETTIDKNGQILLIPEYEADVYMTTLDIPPEAVPRLYDEHRKVCKSLRREFMSDLGFKQLPSRNQKTNELALHFGIYAYNLLRFAGQGKARLKRIRETIRDLPKMVIKEVEAEE
>NZ_CP033687.1|WP_019721979.1|2472311_2473172_-|AraC-family-transcriptional-regulator
MEQYWEKADYSWTDDSIRCFNTPSQRARQLFYYVQEIGHFKAMKPYFTERQHLKSYLLKYTFGGRGKLIYEGREYTLEKGDVFFIDCMNYQHYSTISDEPWEMDWIHFYGPNADAFYGEFMKNGSNVFHAKNGRISQIIDEIMALVETRNAKAEFRISLLIHEMLNEVLIQKYDLAFEEENIPGYIIEAKKFLEDHFKEKITLQDLERVCRLNKYQLSKEFTHYIGIPPIEYLIHFRINTAKRLLRYSNKSVKEIALDVGIEDPPYFNRLFKRKTEMTPLAYRRNG
>NZ_CP033687.1|WP_110133925.1|2473381_2474842_+|rhamnulokinase
MIRNYIAVDIGASSGRLIAGTCRHQKIEIKEIHRFKNGFTKRDGHDRWDIGRLIEEIFTGLEKAKKMGIEACMLGIDTWAVDYVLVDKNGDRLQDPVSYRDPRTVGAIEALTSKYSKEFIYKKTGIQFLELNTLYQLYAEDKNLLEKADKILLIPDYIGYVLTGKAVSEVTNSSTTQMLNLRDKLFDKDLLSHVHVSADKFAKLADAGTILGEIKPEWYQKYDLPACQVVTVATHDTASAVLGTPAEGDSWAFLSSGTWSLLGMELNVPVTSEEAFRENYTNEWGAYGTYRFLKNIMGMWIIQEIARHYDYRYTYAEMAEQAGKCKPFAQFVHVNDPRFNNPENIVKEIQDYCRETGQAVPESIGELTNCIYSSLALCYAVELEKLAAITGRPIDQLYIVGGGSNVSLLNQLTANLANVKVSAGPQEATAIGNLLVQMIAKGDIRDIREGRKIVRQSFAIKSYKPQQGNWKAVIDRYKKTLLETAK
>NZ_CP033687.1|WP_019721982.1|2476141_2476978_+|rhamnulose-1-phosphate-aldolase
MANIKTKLNIIEAPFTQEMMKTTANLYRLGWDERNGGNISYLLKEEEVAPYLDVNAVIRAIPVKFDARALAGKYFIVTGSGKYFKNVADNPAENLGLIRVAQDGQNVELLWGLEGGGMPTSELPSHFMSHIARLEVDPENRIVMHNHATHLLAMTFTHPLDEKAFTRTLWQMCTECLVVFPEGVGIIPWIVPGTNEIGEATAAKMKDYRLVIWPHHGIYGAGRTMDETFGLIETAEKAAQVYTYVQAQGGIKQTITDRQLKDLADAFGVVPREGFLGE
>NZ_CP033687.1|WP_014095526.1|2476981_2477185_+|iron-containing-alcohol-dehydrogenase
MEWRMRPLKNVDIPQSLDKLGVKEEDIPNLAKDAYADVCTGGNPRDTSVEEIEGLYKSMLHDPVVKA
>NZ_CP033687.1|WP_014095525.1|2477287_2477710_+|methylglyoxal-synthase
MKIAFIAHDKKKKEIVNFAVAYEPVFADHELYSTGTTGKRIMEKTNLNITRFNSGPLGGDQEIGAMIAKNEMDLVFFFRDPLTAQPHEPDITALLRLCDVYSIPLATNMGTAELLVQGLMRGDLNWRNLVHEKEKKNRGE
>NZ_CP033687.1|WP_046720824.1|2477873_2478449_+|5-formyltetrahydrofolate-cyclo-ligase
MDKAEMRREMIGWLKRLDLNEKQAIEEKLQQILFSSDIWKISGTVGVTVSQHFEWDTRRIIETGWAQGKTICVPKCVPKEKALVFYQLDDFTQLKKSFFNLLEPEPEETVKIEKQAIDLLIVPGLVFDKKGFRIGFGGGYYDRFLAGFPNQTVSLIHSCQLKAHVPSESYDIPVRQIVTESGMLKVNGGVS
>NZ_CP033687.1|WP_061564830.1|2478445_2479786_+|MFS-transporter
MKSRTFVMISIVLAMLVSSIDATIMNTTMPVIAKELGRFDLYAWAFASYMITSTILSPVAGRLSDLFGRKKVFGFGIVLFFAGSLLCGMSSGMIELIVFRAIQGIGAGFMVPFPAIIAGDLFSVENRGKIQALFTGMWGLSAVLAPLLGSFFVTYLSWRWIFFVNLPVCLISFLTLLPYNEHYAPKKARVDYIGAALFAVAITLLLLVTVVHRNYLLFAATGIIFLLLFYFYEKRQDSPIVPLSMFKNKTFARMNVNSFIGTVALFGASSYVPLFLQKVTGLSLLMSGVALLGSSIGWMAAAVPAGKWILRYGYRRLLLIGNGLLLVSGVCWIFLNPGHGFWYVFLVMIVHGAAFGLLSTVGIIGSQQMVSAHEKGIATSFFMFCRNMGTAIGVTVMGAFLTSGSTYMQGIHHLFLFGFCGSILALLTSFLIHNDASESGKTAANQ
>NZ_CP033687.1|WP_110133926.1|2479958_2481473_-|multidrug-efflux-MFS-transporter
MFFFLQIILTGLFKNKGEILPLQSDYKKFPIMLGLLIGGFIGMFSETALNIALTSLMKDLHITASTVQWLTTGYLLVVGVLVPVSGLMIRWFTTRQLLLSALSAFIIGTLISAVSHTFPFLLIGRLVQGIATGILIPLIFNTVMTIFPPHKRGAALGVVGLVIMFAPAIGPTAAGFILGKLTWQWIFWVVLPFLVAALIISAIFCKNVNEVTRPKIDVLSIVLSTIGFGGIVFGFSSAGDSGWGNAKVIVALAIGVAALTIFSIRQLRMEKPMLNVRVFQHKMFTIGTLMIMIDFSIIMSSMLLLPMYWQSGKLVAVALTGILLLPGGIVNGIVSAISGKLYDIHGAKWLVRIGFLICIVAGAMFICVQTTSSFLFVIAANLLLMIGAPLVMSPAQTNGLNALPREMSPDGSAIMNTAQQVSGAIATALSATLLAAGEHAYTGAGGQHAAAALTNGVQYGFMFTLILAVIGFALSFTVRTVGVFEKPQDQQRKMQLKKETDSPD

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Crispr_ID: NZ_CP033687_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_13

3543038-3543118

Orphan

Consensus_repeat	Method
CTTTGCGAGATCCAATTCGCAAATGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_13

>merge|NZ_CP033687|13|3543038-3543118|CRISPRCasFinder
CTTTGCGAGATCCAATTCGCAAATGGGGGCGTTTTTCCCAAAACCCGTTCGTTCGCTTTGCAAGATCCAATTCGCAAATGG

>NZ_CP033687|13|12|3543038-3543118|CRISPRCasFinder
CTTTGCGAGATCCAATTCGCAAATGG	GGGCGTTTTTCCCAAAACCCGTTCGTTCG
CTTTGCAAGATCCAATTCGCAAATGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_014097647.1\|3544906_3545677_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213260
NZ_CP033687.1\|WP_013860032.1\|3548521_3548758_+\|membrane-protein-insertion-efficiency-factor-YidD	unknown	unknown	gnl\|CDD\|178815
NZ_CP033687.1\|WP_014097650.1\|3540634_3541177_-\|flavodoxin-family-protein	unknown	unknown	gnl\|CDD\|223728
NZ_CP033687.1\|WP_013860030.1\|3547634_3547883_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014097641.1\|3550049_3550208_+\|DUF1540-domain-containing-protein	unknown	unknown	gnl\|CDD\|377869
NZ_CP033687.1\|WP_017551855.1\|3543859_3544867_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|223787
NZ_CP033687.1\|WP_014097657.1\|3531306_3532113_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225176
NZ_CP033687.1\|WP_017551858.1\|3547955_3548405_-\|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl\|CDD\|223854
NZ_CP033687.1\|WP_014097652.1\|3538702_3539092_-\|DNA-mismatch-repair-protein-MutT	unknown	unknown	gnl\|CDD\|240040
NZ_CP033687.1\|WP_017551857.1\|3547004_3547466_-\|nucleoside-triphosphatase-YtkD	unknown	unknown	gnl\|CDD\|131752
NZ_CP033687.1\|WP_061577839.1\|3539575_3540628_-\|DUF2584-family-protein	unknown	unknown	gnl\|CDD\|224423
NZ_CP033687.1\|WP_100183710.1\|3548849_3548978_+\|DUF4021-domain-containing-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_014097649.1\|3541394_3542930_+\|gluconokinase	unknown	unknown	gnl\|CDD\|130381
NZ_CP033687.1\|WP_014097654.1\|3535286_3536498_-\|methionine-adenosyltransferase	unknown	unknown	gnl\|CDD\|235374
NZ_CP033687.1\|WP_014097655.1\|3533157_3535056_-\|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl\|CDD\|223444
NZ_CP033687.1\|WP_017551856.1\|3545663_3546470_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223673
NZ_CP033687.1\|WP_017550244.1\|3536962_3538552_+\|phosphoenolpyruvate-carboxykinase-(ATP)	unknown	unknown	gnl\|CDD\|376517
NZ_CP033687.1\|WP_017551860.1\|3549097_3549988_+\|zinc-ABC-transporter-solute-binding-protein	unknown	unknown	gnl\|CDD\|238499
NZ_CP033687.1\|WP_014097658.1\|3530201_3531296_-\|tetraprenyl-beta-curcumene-synthase-family-protein	unknown	unknown	gnl\|CDD\|378492
NZ_CP033687.1\|WP_014097656.1\|3532271_3532787_+\|gamma-carbonic-anhydrase-family-protein	unknown	unknown	gnl\|CDD\|100051

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_014097647.1\|3544906_3545677_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213260	cd03293, ABC_NrtD_SsuB_transporters, ATP-binding cassette domain of the nitrate and sulfonate transporters. NrtD and SsuB are the ATP-binding subunits of the bacterial ABC-type nitrate and sulfonate transport systems, respectively. 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. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	5.17567e-113
NZ_CP033687.1\|WP_013860032.1\|3548521_3548758_+\|membrane-protein-insertion-efficiency-factor-YidD	gnl\|CDD\|178815	PRK00041, PRK00041, hypothetical protein; Validated.	2.01477e-41
NZ_CP033687.1\|WP_014097650.1\|3540634_3541177_-\|flavodoxin-family-protein	gnl\|CDD\|223728	COG0655, WrbA, Multimeric flavodoxin WrbA [General function prediction only].	2.28697e-28
NZ_CP033687.1\|WP_014097641.1\|3550049_3550208_+\|DUF1540-domain-containing-protein	gnl\|CDD\|377869	pfam07561, DUF1540, Domain of Unknown Function (DUF1540). This family has four conserved cysteines, which is suggestive of a metal binding function.	8.61231e-10
NZ_CP033687.1\|WP_017551855.1\|3543859_3544867_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|223787	COG0715, TauA, ABC-type nitrate/sulfonate/bicarbonate transport systems, periplasmic components [Inorganic ion transport and metabolism].	7.8183e-43
NZ_CP033687.1\|WP_014097657.1\|3531306_3532113_-\|alpha/beta-hydrolase	gnl\|CDD\|225176	COG2267, PldB, Lysophospholipase [Lipid metabolism].	3.67526e-69
NZ_CP033687.1\|WP_017551858.1\|3547955_3548405_-\|DNA-starvation/stationary-phase-protection-protein	gnl\|CDD\|223854	COG0783, Dps, DNA-binding ferritin-like protein (oxidative damage protectant) [Inorganic ion transport and metabolism].	2.37612e-59
NZ_CP033687.1\|WP_014097652.1\|3538702_3539092_-\|DNA-mismatch-repair-protein-MutT	gnl\|CDD\|240040	cd04684, Nudix_Hydrolase_25, Contains a crystal structure of the Nudix hydrolase from Enterococcus faecalis, which has an unknown function. In general, members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	1.40989e-06
NZ_CP033687.1\|WP_017551857.1\|3547004_3547466_-\|nucleoside-triphosphatase-YtkD	gnl\|CDD\|131752	TIGR02705, conserved_hypothetical_protein, nucleoside triphosphatase YtkD. The functional assignment to the proteins of this family is contentious, with papers disagreeing in both interpretation and enzyme assay results. This protein belongs to the nudix family and shares some sequence identity with E. coli MutT but appears not to be functionally interchangeable with it. [DNA metabolism, DNA replication, recombination, and repair].	1.77131e-54
NZ_CP033687.1\|WP_061577839.1\|3539575_3540628_-\|DUF2584-family-protein	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	1.53791e-50
NZ_CP033687.1\|WP_014097649.1\|3541394_3542930_+\|gluconokinase	gnl\|CDD\|130381	TIGR01314, gntK_FGGY, gluconate kinase, FGGY type. Gluconate is derived from glucose in two steps. This model describes one form of gluconate kinase, belonging to the FGGY family of carbohydrate kinases. Gluconate kinase phosphoryates gluconate for entry into the Entner-Douderoff pathway. [Energy metabolism, Sugars].	0
NZ_CP033687.1\|WP_014097654.1\|3535286_3536498_-\|methionine-adenosyltransferase	gnl\|CDD\|235374	PRK05250, PRK05250, S-adenosylmethionine synthetase; Validated.	0
NZ_CP033687.1\|WP_014097655.1\|3533157_3535056_-\|asparagine-synthase-(glutamine-hydrolyzing)	gnl\|CDD\|223444	COG0367, AsnB, Asparagine synthase (glutamine-hydrolyzing) [Amino acid transport and metabolism].	0
NZ_CP033687.1\|WP_017551856.1\|3545663_3546470_+\|ABC-transporter-permease	gnl\|CDD\|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	2.21467e-66
NZ_CP033687.1\|WP_017550244.1\|3536962_3538552_+\|phosphoenolpyruvate-carboxykinase-(ATP)	gnl\|CDD\|376517	pfam01293, PEPCK_ATP, Phosphoenolpyruvate carboxykinase.	0
NZ_CP033687.1\|WP_017551860.1\|3549097_3549988_+\|zinc-ABC-transporter-solute-binding-protein	gnl\|CDD\|238499	cd01017, AdcA, Metal binding protein AdcA. These proteins have been shown to function in the ABC uptake of Zn2+ and Mn2+ and in competence for genetic transformation and adhesion. The AdcA proteins belong to the TroA superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. They are comprised of two globular subdomains connected by a long alpha helix and they bind their ligand in the cleft between these domains. In addition, many of these proteins have a low complexity region containing metal binding histidine-rich motif (repetitive HDH sequence).	1.94198e-97
NZ_CP033687.1\|WP_014097658.1\|3530201_3531296_-\|tetraprenyl-beta-curcumene-synthase-family-protein	gnl\|CDD\|378492	pfam10776, DUF2600, Protein of unknown function (DUF2600). This is a bacterial family of proteins. Some members in the family are annotated as YtpB however currently no function is known.	0
NZ_CP033687.1\|WP_014097656.1\|3532271_3532787_+\|gamma-carbonic-anhydrase-family-protein	gnl\|CDD\|100051	cd04645, LbH_gamma_CA_like, Gamma carbonic anhydrase-like: This family is composed of gamma carbonic anhydrase (CA), Ferripyochelin Binding Protein (FBP), E. coli paaY protein, and similar proteins. CAs are zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide in a two-step mechanism, involving the nucleophilic attack of a zinc-bound hydroxide ion on carbon dioxide, followed by the regeneration of the active site by ionization of the zinc-bound water molecule and removal of a proton from the active site. They are ubiquitous enzymes involved in fundamental processes like photosynthesis, respiration, pH homeostasis and ion transport. There are three evolutionary distinct groups - alpha, beta and gamma carbonic anhydrases - which show no significant sequence identity or structural similarity. Gamma CAs are trimeric enzymes with left-handed parallel beta helix (LbH) structural domain.	2.55616e-77

>NZ_CP033687.1|WP_014097649.1|3541394_3542930_+|gluconokinase
MTYYLGVDIGTTTTKSVLFGEKGKVISMHHAGYPLYSPSPQVAEQNPDEIFRAVIDSMKTAIVKSDIDPSEIKLVSFSSAMHSLIAVDKDGKPLTNCITWADARAAKWAKKIKDEWHGQDIYRRTGTPIHPMSPLSKITWLRHEEQELFKKTFKFIGIKEYIFYRFFGQYVVDYSLASATGLFNLHDLDWDKEALHVAGITADKLSKPVPTTFSLTGLAPEYAVETGIPQDTPFVAGASDGVLSNLGVNAIDPGVVAITIGTSGAIRTVTDKPVTDPKGRIFCYALTENHWVVGGPVNNGGMTFRWVRDELAAAEVETAKRLGIDPYEVLTKIAARVAPGSDGLIFHPYLAGERAPIWNADARGSFFGLGLHHKREHMVRAVLEGVIYNLYTVMLALQEMIGIPKKIQATGGFARSDLWRQMLADIFNQEVVVPESFESSCLGAIVLGMYALDEIDDFSVVSDWIGATHTHRPIPENTAVYEEILPIYIRISRLLEGEYTNIAAFQRKWVK
>NZ_CP033687.1|WP_014097650.1|3540634_3541177_-|flavodoxin-family-protein
MTIAVIYGSSRPRGNTEMLTERAVEGMHVERFYLKDAHILPIEDKRHTDSGFSKVEDDYSILIQHIFMCDTIIFATPIYWYGMSGLMKNFIDRWSQTLRDPQFPDFKKRMAEKKIYVIAVGGDMPRVKGLPLIQQFAYIFDFLGMRFDGYILGEGNKPGDIVQDKEAIFAADQLNEALKR
>NZ_CP033687.1|WP_061577839.1|3539575_3540628_-|DUF2584-family-protein
MKTVIEKQLFPSPNPHVRMYLVTYWSDGLKVKGLLAEPDDGRVYDGFLYLRGGIKSVGMVRPARIGEFASEGFIVFAPFYRGNWGGEGDEDFGGDDMHDAYFGFDVLMEHERVSGRVHVFGFSRGGIMALGTAEARPAASIVTWGGVSDVALCYAERVDLRKMMKRVIGGTPDKYPERYRVRTPLYKLGQIGCPVLVIHGEKDQNVSVEHAIRLEHGLKQLGKSVETWYFPELGHHFPPPVNRRIVHAASVWMKRHSAHDTIEATTEVSRMGMPMELDTMLVTNGKEERIEQNLFLLKQPGYCVYPLDTPVEIRKKKEHGPSGSAVIRKLEWENNTTIVHYELVSLNTPN
>NZ_CP033687.1|WP_014097652.1|3538702_3539092_-|DNA-mismatch-repair-protein-MutT
METDYKKACGAYAVIFDAKKEKVGVVPSGSGYRLPGGEISRGESELACLMRTVGAELEIAGFLGKAAQETGARSMDEGLFYLGKWEQPRKGSHNLEWLNLHEAVEKMAGAHHQWAVQEGISAVQTSTWF
>NZ_CP033687.1|WP_017550244.1|3536962_3538552_+|phosphoenolpyruvate-carboxykinase-(ATP)
MKMDLIGASDDLKFLLSGENVRMQLSVPQLMEKIIERKEAVLTTEGAISAATGKYTGRSPKDKFIVVDSESKDRVDWGKINQPVSPGVFNRLYEKMVRHLKGKDEIFVFKGFAGADPKSRLPIQTVNEFAWHNLFAHQLFIRPDAEELYQHDAQFTILSAPLFKADPALDGTHSEAFIMISLERRIILIGGTEYAGEMKKSIFSIMNYLLPQKGILPMHCSANTGKNGDTALFFGLSGTGKTTLSADPERALIGDDEHGWSDSGVFNIEGGCYAKCIGLTEEKEPQIYQAIRFGTVLENVVVDPVSRKPQYDNNALTENTRAAYPIENIGNIARSGMAGHPSTIIFLTADASGVLPPISRLTKEQAMYHFLSGYTSKLAGTERGVTRPEAVFSTCFGAPFLPLEPAVYAEMLGEKVDRHNVQVFLVNTGWTGGPYGTGSRMKLSDTRAMVRAAINGKLKDTETRQDDIFGLHIPVHIEGVSDDVLYPADTWTDKQAYREKAFELAARFKENFRQFSVPDDIEKLGGPLI
>NZ_CP033687.1|WP_014097654.1|3535286_3536498_-|methionine-adenosyltransferase
MLKGRHLFTSESVTEGHPDKICDQISDAILDAILEKDPNARVACETSVTTGLVLVTGEISTNTYVDIPKVVRKTIKEIGYTRAKYGFDAETCAVLTSIDEQSEDIARGVNQALEAREGGMSDEEIEAIGAGDQGLMFGFACNETEELMPLPISLAHKLARRLAELRKQEVIPYLRPDAKTQVTVEYDENNQPARIDTIVISTQHDPDTSAGQIQEDMKKYVIEPVVPAHLLDADTKYLINPTGRFVIGGPQGDAGLTGRKIIVDTYGGYARHGGGAFSGKDPTKVDRSAAYAARYVAKNIVAAGLAEKCEVQLAYAIGVAKPVSISIDTFGTGKVPEKVLIEAVEAHFDLRPAGIIKMLDLRRPIYRQIAAYGHFGRDDLDVPWEKTDKAGALNEFARNHIGK
>NZ_CP033687.1|WP_014097655.1|3533157_3535056_-|asparagine-synthase-(glutamine-hydrolyzing)
MCGFIGCVHDHPVTLSDEDRQQFKQMNHMIEHRGPDDEGFYEDEHIQFGFRRLSIIDIEAGHQPLTYENERYWIIFNGEIYNYVELREELIKEGMTFETNSDTEVILAMYSRYGEKAIGRLRGMFGFAIWDKQEQTLCGARDPFGIKPFFYYEDGDKMYFGSEKKSILLAMEKPELNYDAVQYYLTYQFVPEPFTMTKGIRKLEPGHYFVKKIGKPMEIKRYWKASFHPVHKSEDEFIQEVRDVMIDSVKVHMRSDVPVGAFLSGGIDSSITASIAKQFHPGIKTFSVGFERDGYSEIDVAKETAEKLGVENISYVITPEEYMKELPKIIWHMDDPLADPACVPLYFVAREARKYVTVVLSGEGADELFGGYNIYREPQSLEVFDKIPAAGKSILKALAKVLPEGVKGKSFIERGVTPMEDRYIGNAKMYTEEEKRDLLLTYNNSLDYRDITKPLYNETKGYDPVNRMQYIDIHTWMRGDILLKADRMTMAHSLELRVPFLDKEVFRVASQIPASLKTSHNTTKYVLRKAAEGIVPEHVLNRKKLGFPVPIRHWLKDEMHDWAAEIIKTSPTDDIINKQYVLKLLEDHCAGKLDYSRKIWTVLIFMLWHAVYMEDKYDFQKGAQGRLAGASL
>NZ_CP033687.1|WP_014097656.1|3532271_3532787_+|gamma-carbonic-anhydrase-family-protein
MIYAYNGKTPLIAPTAYIADNVTVTGDVEIGDESGIWFGTVIRGDVAPVKIGQKVNVQDNCVLHESPQTPLILEDEVTVGHQVILHSCHVRTKALIGMGSIILDGAEIGEGAFIGAGSLVTPGKKIPPHTLAFGRPAKVIRELTEKDIQDMRRIVREYAEKAQYYKNSVGR
>NZ_CP033687.1|WP_014097657.1|3531306_3532113_-|alpha/beta-hydrolase
MWKWEADENPKAVIVIVHGAMEHHRRYSWLIEMWRSSGYHVVMGDLPGHGMTSRAKRGHIDSFDEYTTEIKEWVTAAYQFDLPIFLLGHSMGGLAVIRLLEQEHLKIAGVILSSPCLGLVQYPSKLLGLLSIGLNRIAPGLRFNSPLTVQMATRNKDIQMQAVNDSLMLTKVSVRWYRELLAAMRQAQMDTVRLPDVPFLVMQAGNDKIVDKGAVVNWFNQTSVSEKLYKEWPKCYHEIFNEPEREDVFLYAKNFVENRLRTLGYILE
>NZ_CP033687.1|WP_014097658.1|3530201_3531296_-|tetraprenyl-beta-curcumene-synthase-family-protein
MTIPSYPISLMAQVYRRVMPAVHRELHYWREKARQIPNDELKTQALASIQHKTFHCEGGSILGLLAMEERTAAFRFIVAYQTISDYLDNLCDRSTSLDPVDFRALHESMSDALTVGAPLKNYYRYRLDQDDGGYLHELVRTCQVVLSRIPQYKAIQPYLLELCRYYSDLQVHKHVRVEERVPRLKEWFLRYKPDFPDMEWYEFSACSGSTLGIFCLVSYALRDDFRPEYATIIRDGYFPYIQGLHILLDYFIDQDEDKKGGDLNFCFYYPSEEELFKRLKHFLQEADKHTARLPNEKFHKLINRGLLAVYLSDEKVKKQRSVQKLSRKMIKFAGSISLFFYFNGKMYRAIKNMIPASLAKTIVK
>NZ_CP033687.1|WP_017551855.1|3543859_3544867_+|ABC-transporter-substrate-binding-protein
MKKWLKSGCTLLLAALLAFSLSACGTNGSKKKALQKVRVAEVTRSVFYTPLYVALEKGYFKEEGLDIKLTTTWGGDKTMTALLSGGTDIALVGSETSIYVYKQKAADPVINFAQLTATDGTFLVSRKKIDHFSWDMLKGTTFLGQRKGGMPQMVGEFVLKKHGIDPHKDTKLIQNIDFANVANAYASGTGDFVQLFEPTASTMEKEGKGYIVASFGKESGAVPYTTFMAKQSYLKEHEKTAVEFVRALLKAGKWVQETDAETVAKTVQPYFKDTKTDMLASSIERYRSQGSFSSDMILTKSGWNTIQDIMKEAGELDHTVPYDKLVNASIVKKAK
>NZ_CP033687.1|WP_014097647.1|3544906_3545677_+|ABC-transporter-ATP-binding-protein
MHFLTVQNVNHTYFTAKQATKALENISFQMEEGEFVSLLGPSGCGKTTLLSILAGLLQPTAGIVQIDGKLPGSRQSSIGYMLQQDYLFPWKTIEENIMIGLKLEKRLNPESRKHALGLLQTIGLAGTEKQYPRQLSGGMRQRAALVRTLAVDPKILLLDEPFSALDFQTKLKLEDLVFDTLKQFHKTAVLVTHDIGEAIAMSDRILLLASKPGRLYKIFDVPTELRRLRPFEARSQKIYSELFNDIWKELESLENS
>NZ_CP033687.1|WP_017551856.1|3545663_3546470_+|ABC-transporter-permease
MKTAENTALRHEDYLAAMRKEKRRVRFFQLFILIVFFCLWEVASRLHWIDPLIFSSPSKVWALLVAKLEDGSLYVHLGITVFETVMGFILGTVLGAALAAVLWWSPFLSKILDPYLVVLNAMPKVALGPILIVSMGPGFSSIVAMGVIISVIVTTIVIYTAFRDVDPNYTKVLHSFGASRLQVFREAIFPASIPVIISTLKVNVGLAWVGVIVGEYLVSSKGLGYMIIYGFQVFNFTLVMLSMILIAIVATIMYQLVGWLEKKLVKDR
>NZ_CP033687.1|WP_017551857.1|3547004_3547466_-|nucleoside-triphosphatase-YtkD
MYRFTDLNGNPVTFIFEKNAFPIEPQHVLVLARYRGNWLLTRHPKRGLEFPGGKREAGETVREAAERELYEETGGIPENLQYIGEYCVDDQVRGPFVKAVFYADIGRLETKHDYLETDGPVLVEGDLVEKLQSSSFSFLMKDGVVETALRHVE
>NZ_CP033687.1|WP_013860030.1|3547634_3547883_+|hypothetical-protein
MRLVDELFELYRDRLTGDEEDLDAISAAVVENYNRKDLLGIVREMSTAELEHFIGLYILETLKDKFSDYAGFDAYPTTKYLQ
>NZ_CP033687.1|WP_017551858.1|3547955_3548405_-|DNA-starvation/stationary-phase-protection-protein
MAENEQLMEILNKQVANWTVLYTKLHNYHWYVKGPNFLSLHAKFEELYNLANDYLDELAERLLALNGNPVATLKGSLELSSVQEASGNESTEEMVQATANDFAMIAKELEEAIGLANRIGDDATADMFINIQETLDKNIWMLNAFLGRR
>NZ_CP033687.1|WP_013860032.1|3548521_3548758_+|membrane-protein-insertion-efficiency-factor-YidD
MLKFIFIKLIRFYQLAISPLFPPSCRFQPTCSNYGLEAVKRFGALRGGYLAIRRILKCHPFHAGGYDPVPDQWPVKKH
>NZ_CP033687.1|WP_100183710.1|3548849_3548978_+|DUF4021-domain-containing-protein
MFFMEEKKEQQKKSGDFGADPDEQAINGDYGMLETEEEDKKD
>NZ_CP033687.1|WP_017551860.1|3549097_3549988_+|zinc-ABC-transporter-solute-binding-protein
MKKLFPVLLAFTMLFVTACANKQESKQDHKISVYTTVYPLEYVTQQIGGKYVSVKTIYPPGTDEHTYEPSQKDILKLADSDFFFYIGLGLEGFANKAKQVLEGQNVKMMALGDRLPVPDKTSTKADPHVWLDPIYVKQMAGMITTQLSKKMPKQKTYFKKNYAQLAKKLDQVNAAYKQAVEKSDNKELVVSHAAYGYWVKRYGIKQIPIAGLSTSDEPSQKQLENIIQKVKQDHISYIVFEKNVPSKIAEVVQQETNTKAVYIHHLGVRTNAEIKAHKDYFTLMDDNLKALEKALQ
>NZ_CP033687.1|WP_014097641.1|3550049_3550208_+|DUF1540-domain-containing-protein
MAKDVLCEVRNCVFWEEGNLCSAEEIYIVSHTGTQAENQRETDCKTFESMFS

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Crispr_ID: NZ_CP033687_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP033687_14

3560097-3560197

Orphan

Consensus_repeat	Method
GCGGGTGATGGGAATCGAACCCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP033687_14

>merge|NZ_CP033687|14|3560097-3560197|CRISPRCasFinder
GCGGGTGATGGGAATCGAACCCACGACAACAGCTTGGAAGGCTGTGGTTTTACCACTAAACTACACCCGCAGCAAAGGGCGGATGATGGGAATCGAACCCA

>NZ_CP033687|14|13|3560097-3560197|CRISPRCasFinder
GCGGGTGATGGGAATCGAACCCA	CGACAACAGCTTGGAAGGCTGTGGTTTTACCACTAAACTACACCCGCAGCAAAGG
GCGGATGATGGGAATCGAACCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP033687.1\|WP_035183998.1\|3558674_3559598_+\|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	unknown	unknown	gnl\|CDD\|235695
NZ_CP033687.1\|WP_026684902.1\|3553668_3554487_-\|1,4-dihydroxy-2-naphthoyl-CoA-synthase	unknown	unknown	gnl\|CDD\|180958
NZ_CP033687.1\|WP_104851084.1\|3571223_3572909_-\|IS1634-family-transposase	unknown	unknown	gnl\|CDD\|227708
NZ_CP033687.1\|WP_110134053.1\|3572952_3574248_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273736
NZ_CP033687.1\|WP_017551860.1\|3549097_3549988_+\|zinc-ABC-transporter-solute-binding-protein	unknown	unknown	gnl\|CDD\|238499
NZ_CP033687.1\|WP_061565856.1\|3557074_3558409_-\|isochorismate-synthase	unknown	unknown	gnl\|CDD\|224091
NZ_CP033687.1\|WP_014097641.1\|3550049_3550208_+\|DUF1540-domain-containing-protein	unknown	unknown	gnl\|CDD\|377869
NZ_CP033687.1\|WP_035183995.1\|3555327_3557073_-\|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	unknown	unknown	gnl\|CDD\|236020
NZ_CP033687.1\|WP_061565795.1\|3578480_3578867_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|349949
NZ_CP033687.1\|WP_061577719.1\|3575025_3575931_-\|DMT-family-transporter	unknown	unknown	gnl\|CDD\|223769
NZ_CP033687.1\|WP_035188985.1\|3551636_3553091_-\|o-succinylbenzoate--CoA-ligase	unknown	unknown	gnl\|CDD\|235146
NZ_CP033687.1\|WP_081106251.1\|3576846_3577971_-\|DUF1646-family-protein	unknown	unknown	gnl\|CDD\|285138
NZ_CP033687.1\|WP_100183710.1\|3548849_3548978_+\|DUF4021-domain-containing-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_035183985.1\|3550536_3551640_-\|o-succinylbenzoate-synthase	unknown	unknown	gnl\|CDD\|239433
NZ_CP033687.1\|WP_046721937.1\|3569449_3570100_-\|putative-bacteriocin-export-ABC-transporter	unknown	unknown	gnl\|CDD\|188353
NZ_CP033687.1\|WP_035191286.1\|3567958_3569122_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP033687.1\|WP_061577841.1\|3554527_3555331_-\|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase	unknown	unknown	gnl\|CDD\|274729
NZ_CP033687.1\|WP_035191149.1\|3574545_3574725_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP033687.1\|WP_013860047.1\|3576021_3576711_+\|MgtC/SapB-family-protein	unknown	unknown	gnl\|CDD\|224204
NZ_CP033687.1\|WP_110134052.1\|3570101_3571082_-\|DUF1430-domain-containing-protein	unknown	unknown	gnl\|CDD\|273736

Protein	Function_ID	Function_description	E-value
NZ_CP033687.1\|WP_035183998.1\|3558674_3559598_+\|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	gnl\|CDD\|235695	PRK06080, PRK06080, 1,4-dihydroxy-2-naphthoate octaprenyltransferase; Validated.	4.94633e-126
NZ_CP033687.1\|WP_026684902.1\|3553668_3554487_-\|1,4-dihydroxy-2-naphthoyl-CoA-synthase	gnl\|CDD\|180958	PRK07396, PRK07396, dihydroxynaphthoic acid synthetase; Validated.	0
NZ_CP033687.1\|WP_104851084.1\|3571223_3572909_-\|IS1634-family-transposase	gnl\|CDD\|227708	COG5421, COG5421, Transposase [DNA replication, recombination, and repair].	1.77023e-40
NZ_CP033687.1\|WP_110134053.1\|3572952_3574248_-\|hypothetical-protein	gnl\|CDD\|273736	TIGR01654, unnamed_protein_product, bacteriocin-associated integral membrane (putative immunity) protein. This model represents a family of integral membrane proteins, most of which are about 650 residues in size and predicted to span the membrane seven times. Nearly half of the members of this family are found in association with a member of the lactococcin 972 family of bacteriocins (TIGR01653). Others may be associated with uncharacterized proteins that may also act as bacteriocins. Although this protein is suggested to be an immunity protein, and the bacteriocin is suggested to be exported by a Sec-dependent process, the role of this protein is unclear. [Cellular processes, Toxin production and resistance].	1.59365e-07
NZ_CP033687.1\|WP_017551860.1\|3549097_3549988_+\|zinc-ABC-transporter-solute-binding-protein	gnl\|CDD\|238499	cd01017, AdcA, Metal binding protein AdcA. These proteins have been shown to function in the ABC uptake of Zn2+ and Mn2+ and in competence for genetic transformation and adhesion. The AdcA proteins belong to the TroA superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. They are comprised of two globular subdomains connected by a long alpha helix and they bind their ligand in the cleft between these domains. In addition, many of these proteins have a low complexity region containing metal binding histidine-rich motif (repetitive HDH sequence).	1.94198e-97
NZ_CP033687.1\|WP_061565856.1\|3557074_3558409_-\|isochorismate-synthase	gnl\|CDD\|224091	COG1169, MenF, Isochorismate synthase [Coenzyme metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	9.13781e-137
NZ_CP033687.1\|WP_014097641.1\|3550049_3550208_+\|DUF1540-domain-containing-protein	gnl\|CDD\|377869	pfam07561, DUF1540, Domain of Unknown Function (DUF1540). This family has four conserved cysteines, which is suggestive of a metal binding function.	8.61231e-10
NZ_CP033687.1\|WP_035183995.1\|3555327_3557073_-\|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	gnl\|CDD\|236020	PRK07449, PRK07449, 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase; Validated.	0
NZ_CP033687.1\|WP_061565795.1\|3578480_3578867_-\|MFS-transporter	gnl\|CDD\|349949	cd06174, MFS, Major Facilitator Superfamily. The Major Facilitator Superfamily (MFS) is a large and diverse group of secondary transporters that includes uniporters, symporters, and antiporters. MFS proteins facilitate the transport across cytoplasmic or internal membranes of a variety of substrates including ions, sugar phosphates, drugs, neurotransmitters, nucleosides, amino acids, and peptides. They do so using the electrochemical potential of the transported substrates. Uniporters transport a single substrate, while symporters and antiporters transport two substrates in the same or in opposite directions, respectively, across membranes. MFS proteins are typically 400 to 600 amino acids in length, and the majority contain 12 transmembrane alpha helices (TMs) connected by hydrophilic loops. The N- and C-terminal halves of these proteins display weak similarity and may be the result of a gene duplication/fusion event. Based on kinetic studies and the structures of a few bacterial superfamily members, GlpT (glycerol-3-phosphate transporter), LacY (lactose permease), and EmrD (multidrug transporter), MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement. Bacterial members function primarily for nutrient uptake, and as drug-efflux pumps to confer antibiotic resistance. Some MFS proteins have medical significance in humans such as the glucose transporter Glut4, which is impaired in type II diabetes, and glucose-6-phosphate transporter (G6PT), which causes glycogen storage disease when mutated.	1.05771e-06
NZ_CP033687.1\|WP_061577719.1\|3575025_3575931_-\|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].	4.0558e-13
NZ_CP033687.1\|WP_035188985.1\|3551636_3553091_-\|o-succinylbenzoate--CoA-ligase	gnl\|CDD\|235146	PRK03640, PRK03640, o-succinylbenzoate--CoA ligase.	0
NZ_CP033687.1\|WP_081106251.1\|3576846_3577971_-\|DUF1646-family-protein	gnl\|CDD\|285138	pfam07854, DUF1646, Protein of unknown function (DUF1646). Some of the members of this family are hypothetical bacterial and archaeal proteins, but others are annotated as being cation transporters expressed by the archaebacterium Methanosarcina mazei.	1.567e-108
NZ_CP033687.1\|WP_035183985.1\|3550536_3551640_-\|o-succinylbenzoate-synthase	gnl\|CDD\|239433	cd03317, NAAAR, N-acylamino acid racemase (NAAAR), an octameric enzyme that catalyzes the racemization of N-acylamino acids. NAAARs act on a broad range of N-acylamino acids rather than amino acids. Enantiopure amino acids are of industrial interest as chiral building blocks for antibiotics, herbicides, and drugs. NAAAR is a member of the enolase superfamily, characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	0
NZ_CP033687.1\|WP_046721937.1\|3569449_3570100_-\|putative-bacteriocin-export-ABC-transporter	gnl\|CDD\|188353	TIGR03608, L_ocin_972_ABC, putative bacteriocin export ABC transporter, lactococcin 972 group. A gene pair with a fairly wide distribution consists of a polypeptide related to the lactococcin 972 (see TIGR01653) and multiple-membrane-spanning putative immunity protein (see TIGR01654). This model represents a small clade within the ABC transporters that regularly are found adjacent to these bacteriocin system gene pairs and are likely serve as export proteins. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Unknown substrate].	1.40778e-87
NZ_CP033687.1\|WP_035191286.1\|3567958_3569122_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.65403e-14
NZ_CP033687.1\|WP_061577841.1\|3554527_3555331_-\|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase	gnl\|CDD\|274729	TIGR03695, menH_SHCHC, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase. This protein catalyzes the formation of SHCHC, or (1 R,6 R)-2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate, by elmination of pyruvate from 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC). Note that SHCHC synthase activity previously was attributed to MenD, which in fact is SEPHCHC synthase. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	8.56654e-120
NZ_CP033687.1\|WP_013860047.1\|3576021_3576711_+\|MgtC/SapB-family-protein	gnl\|CDD\|224204	COG1285, SapB, Uncharacterized membrane protein [Function unknown].	1.46137e-50
NZ_CP033687.1\|WP_110134052.1\|3570101_3571082_-\|DUF1430-domain-containing-protein	gnl\|CDD\|273736	TIGR01654, unnamed_protein_product, bacteriocin-associated integral membrane (putative immunity) protein. This model represents a family of integral membrane proteins, most of which are about 650 residues in size and predicted to span the membrane seven times. Nearly half of the members of this family are found in association with a member of the lactococcin 972 family of bacteriocins (TIGR01653). Others may be associated with uncharacterized proteins that may also act as bacteriocins. Although this protein is suggested to be an immunity protein, and the bacteriocin is suggested to be exported by a Sec-dependent process, the role of this protein is unclear. [Cellular processes, Toxin production and resistance].	5.24748e-31

>NZ_CP033687.1|WP_035183998.1|3558674_3559598_+|1,4-dihydroxy-2-naphthoate-polyprenyltransferase
MNAQSSPAIGPDKGWRIWWQLTRPHTLTAGFVPVILGTVLALGIARINLLLFAAMLVATLLIQAATNMFNEYYDYKRGLDTEHSVGIGGAIVRNGIKPKTVLHLAFAFFGAAMLIGVYICSQSSWWIAVIGTVCMLVAYLYTAGPFPISSTPLGELISGFFMGVIIILISFFIQTKTITWPIVFISIPIMILIGAIMLSNNIRDLDGDKANGRKTIAILLGRKGAILLLAAMFALSYLWMAGLVLFGVVTPWVLLVFVSTPKPVRAIKGFIGKSEPLQMLPAMKATAQTNTIFGVLLSISFLIDHFI
>NZ_CP033687.1|WP_061565856.1|3557074_3558409_-|isochorismate-synthase
MKEKTAPALKLVSKVIKCRTAPDPLRLFTAGAAHFYGSRFFWQDADRETVFVGFGCVWSCTVTASDGFAQMEDEWRNLKGAGEVYSGTGETGTGPVLFGGFAFDGTVAKQEWKTFGQGIFRVPQILFTFKKDAVFLTVNGCGGTESVQEAEETARTLLNGSTAFLPALPLLKAVKEIGSDEWKKSVATAVEFIREGRMDKVVLARKLELAFDGVASPDAVLAALSAQQHDSYLFVLEEGSESFIGASPERLVKKTGRHILSTCLAGSIKRGRNEAEDLELGKALLSDQKNLSEHGFVVSMIRQVLEPFCNGLNVPDEPVLMRMRDIQHLYTPVTGTVKDKDTTLFQLVKALHPTPALGGIPRQPAMEAIRLLEKMDRGLYGAPIGWVDYRGSGEFCVGIRSGLLKEDRASLYAGCGVVKESEPEEEYKETSVKFTPMLRALGGK
>NZ_CP033687.1|WP_035183995.1|3555327_3557073_-|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase
MEHQEIMTTYLAAFIRQLSAMGIRYAVVSPGSRSTPIAMLLAEHPDFQIYMDIDERSAAFFALGLAKEKRKPVVLLCTSGTAAANYYPAVAEANISRVPLIVLTADRPHELRNVGAPQAIDQIRLYGTHVKWFEEMPLPEAEEEVLQFVRQTAARAVVTALQQPAGPVHLNFPLREPLVPVLKPSPFAGEVPVPAIENFSGTLRLSEETVEIVAKEIREKDRGLIICGPIDIPGFAEAVVALSEKTGYPVLADPLSQLRSGRHGKERIIENYDSLLKDPKWAGRLAPNVVIRFGAMPVSKPLTLLLKKVKTAAHYIVDGGNGWRDPVKRGTTVVYSDEIDFCKKLSNIIVMNPVSEWFTMWEKLNQQARQIVTASLEVEKTFDEGKTVTELAAALPDGSTLFVGNSMPIRDVDTFFQATDKKIRILANRGANGIDGVVSSATGVSAGCGKAFLLIGDLSFFHDLNGLLMTKMHKLNLCVILINNNGGGIFSFLPQADEPEKFEQLFGTPTDLAFEYAVKMYGGSYIQPQNWDQFRAALSEYKGGLQVIEVRTNRAKNVETHRKIWSQVSREMERYFQGEQQ
>NZ_CP033687.1|WP_061577841.1|3554527_3555331_-|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase
MRINGLEYHVETAGDGEPLLLLHGFTGNGNTWNDTVSILRDEFRCIVVDIIGHGKTEKPDDPGRYDITKAAADLRAVLLALGIRRASVLGYSMGGRLALTFAVQYPQMVDKLVLESASPGLKTEAERLARRERDEQLAERILTGGMEAFVSHWENLPLFASQKQLPAEVQRKIRKQRLENDPSGLANSLRGMGTGAQPSWWERLSELHFPVLLAAGEWDAKFCRIAGEMEERLPHAKKIIFSHAGHAIHVEDPKKFGTMVKGFLKNC
>NZ_CP033687.1|WP_026684902.1|3553668_3554487_-|1,4-dihydroxy-2-naphthoyl-CoA-synthase
MAVEWKTEHEYEDILYESYNGIAKITINRPHVRNAFRPETVTEMYDAFSRARDDANIGVIILTGMGEKAFCSGGDQKVRGNGGYVGSDNIPRLNVLDLQHLIRVIPKPVIAMVAGYAIGGGHVLHVVCDLTIAADNAIFGQTGPKVGSFDGGYGAGYLARIVGHKKAREIWYLCRQYNAQEALEMGLVNAVVPYEKLEEETIKWAEEILEKSPMAIRFLKAAFNADTDGLAGLQQFAGDATLLYYTTDEAKEGRDAFKEKRKPDFGQFPRFP
>NZ_CP033687.1|WP_035188985.1|3551636_3553091_-|o-succinylbenzoate--CoA-ligase
MLPNFLKQRAYLTPNRIALISQGTSLTFAGLYEKAKETARKLSGCGMQAEDTAAVLLNSRAETAVILHALQQLRVRTLFLNHRLTPAEMQYQLTDSGAKWLITEKSFREKAEVLNETATVIQSEALDDLPAAGYEERAEFAFEDVCSIMYTSGTTGKPKGVLQTYGNHWWSAAGSALNLGVREDDTWLCAVPLFHISGFSILMRSVFYGMTVYLMEKFDEKETAKLLKSGRITTMSVVTNMLQRLLRELGQERLHPNFRCLLLGGGPAPRPLLEACAEKNIPVFQSYGMTETASQTVTLAPEDSLRKIGSAGKPLFPAQIRIVSDGKVCGPFEHGEIAVKGPNVTIGYLNRPDANQKSFRDGWFFTGDIGYLDDEGFLYVLDRRSDLIISGGENIYPAEIEEVLLAHPDILEAGVIGVEDEKWGQVPAAFIVTKRAVQERELQAFCETRLAKFKIPKKVYAVPALPRNASNKLVRRKLLELLPS
>NZ_CP033687.1|WP_035183985.1|3550536_3551640_-|o-succinylbenzoate-synthase
MIGIEKVTLSVIKMPLKSPFENALEKVTEREAILLEVTDNDGVTGFGEAVAFSTPWYTEETVQTCFHMLKDVLVPLLREKPVAHPKEVSGRFQSVRRNHMAKAAIETAIWDLYAKKKQKPLWQLIGGARDHVDAGVAVGSHDTAEALRQIAAFVDEGYKRVKVKIKPGHDEAFIREIRHAFPDLALMADANSAYTLADAPRLKRLDRYGLLMIEQPLAADDIVEHAALQKQLETPVCLDESIVTYHDAESALRLGSFRVLNIKIGRVGGLYPAIRLHDLCASRGIPVWCGGMIEFGVSRAFNLALASLPGFTIPGDISSSSRFWEKDIIEPEITVENGQIRLPDRPGTGFEIDRAYVEKIRTYTETI
>NZ_CP033687.1|WP_014097641.1|3550049_3550208_+|DUF1540-domain-containing-protein
MAKDVLCEVRNCVFWEEGNLCSAEEIYIVSHTGTQAENQRETDCKTFESMFS
>NZ_CP033687.1|WP_017551860.1|3549097_3549988_+|zinc-ABC-transporter-solute-binding-protein
MKKLFPVLLAFTMLFVTACANKQESKQDHKISVYTTVYPLEYVTQQIGGKYVSVKTIYPPGTDEHTYEPSQKDILKLADSDFFFYIGLGLEGFANKAKQVLEGQNVKMMALGDRLPVPDKTSTKADPHVWLDPIYVKQMAGMITTQLSKKMPKQKTYFKKNYAQLAKKLDQVNAAYKQAVEKSDNKELVVSHAAYGYWVKRYGIKQIPIAGLSTSDEPSQKQLENIIQKVKQDHISYIVFEKNVPSKIAEVVQQETNTKAVYIHHLGVRTNAEIKAHKDYFTLMDDNLKALEKALQ
>NZ_CP033687.1|WP_100183710.1|3548849_3548978_+|DUF4021-domain-containing-protein
MFFMEEKKEQQKKSGDFGADPDEQAINGDYGMLETEEEDKKD
>NZ_CP033687.1|WP_035191286.1|3567958_3569122_+|glycosyltransferase-family-4-protein
MKPIATPFPPVSMGDIHVYDDIIQYFNFKQVKQALPHRPKSITFVTTGIIPYDGGQTTMLHLGTELSKLGFQVYYLSYFSQPRKAMEINAEFNYAGYQGTCLDVSALKTHQSDIWIGTLWESVYVFKDKPGYKMYFVQDYEPYFYPFGDRYYLAKKTYELGLHMVSLGPWCAEMIEKECRVQSPLDVIRFPVDMEQYPFHPRNFLDYKKKKEFRIAVYTKWDSPRRAPISIQIVLNNFLKLCQKHGYQLDIVYFGTDQSAQFINGKNLGQLTKKELHELYLKSDFGIAPSMTNFSLVPYEMMSSGLPVIDFYEGTGRSFMPENCALFCHLDEQSLFQTFQNAISHPGHIAETVKNAQAHLNTVTWKETIKDFINVINAIQSKNRIVS
>NZ_CP033687.1|WP_046721937.1|3569449_3570100_-|putative-bacteriocin-export-ABC-transporter
MVICEMQNIYKSFGDKIVFENFNILINQGDFLCIAGNSGTGKSTLLNMMGLLERPDSGTINVFGKQNVKPNSHTAQKLLRHKIGFLFQNFALIDDKSVNYNLDLACVDKKRWDKNSKTQLLEKLQLDVSLNKKVYHLSGGEQQRLALARLIMKDCDFILADEPTGSLDQTNRNTVLDILSQLNHNGKTIVIVSHDPFVMERCQRVVNLNSPSKAEA
>NZ_CP033687.1|WP_110134052.1|3570101_3571082_-|DUF1430-domain-containing-protein
MRNVGYSYLNQKFHAIYIDSDLYTEDSLKLNARLNIIKYIEVNPNYLNKYPILDTEGNKIVINEENEHTVILVPEQYKKKEDFNLDYFTSFREEMYKLHRDFYHQADKAKSTKIDFIYMKSGQKIFSMNPDVMPNNNNNIVDPIIQVMTEGNALVPDIHYTSSGNQTLFIKLINSDSERTYKQLLPKLQEFKLDDNLPYLVKSNEVILSEINDLHSEAKIIGYILLFMFLILTILLLQNIYLQFERNKFEFFLKKAFGHTFVEKYKKVLLLLLLTDILEFIGGIFLIDSNFFNIFIVKVLIELGLVILIIIYFERKNTVQVLKEGV
>NZ_CP033687.1|WP_104851084.1|3571223_3572909_-|IS1634-family-transposase
MSDQILTLHVGPSQLLSKLCDEIELEKTINDLVKWDSVRCHISPGTRIKALVLNILCSGKPLYKVHEFYQNLDSEMLFDTSISPDQLNDDALGRALDYLYKAEAWKVYSTLALKALKKLNLPIGVLHNDTTSISVYGEYKQPKEDGLQITYGYSKAHRPDLKQIVLGMGVTPERIPILAKVENGNTSDKSWNVEFIQKMRKILSHEDWKNLIYQADSALITTENLAEIQQQNLSFISRLPDTFGLSTELKKEAWLLNNWERVGSLSNKKDAAIYQIQAFERQIQNLPYRFLVVHSNNLDQRKEKTLNRAIEKEEIQLKKEIEKLSKVIFHCKEDALEAIQSFKKKQKASYFCYKLNVQMSDQPIKRKKRGRPKKDEQTKQEQIYQIQLESFEKDHDFIENKKKMLSTFVLITNKLDEETLSNQEVLRVYKGQSAAETRFRLIKDSQMIDAIYLKTPERVEALGIVYVMALLIYGILEYRVRKELKEKNLSLILKGKRKLYQPTGQALLEQLEDITVILINQNQQKIRLLPDNIDSQAKKIIELCGYDVSIYVSKNVENKGE
>NZ_CP033687.1|WP_110134053.1|3572952_3574248_-|hypothetical-protein
MKRFLTIFSFIMFITLALSNYYSYQAESYQKLVDPSGDYTYNFEIPEDVVNANPQRLTLLKKAAKKNKVNIIRTVSYYDDKKEKTYTKAYLFLSTDTRLFDKMKIVNGRGLTIKDMMNPDRFISTDKTASKDQVGVIKNFGGKNSYSIHVLDNITANYKYSGLYKLEAASEEQYNKFIHDYVSYVNKAIGKNYFRPEMYTNITRSTKTEINNAMDTKMIAIFFVAIMILTFLFYLISRTKEISVMRLNGYTIKSISLKIFIQFFTKVFLASSLIIIPWMFLIKDNNFAFVKKVYITNFIIYVILIVVLTSLCFLYAKNIRIASSIKGKKPIGIIAILNGIFKVVVSITILIMAVNLLTNLTQINQKQNSLHHWSEFHNYGVFYPVKTGNDSDVIREGKYPLDIPAYKLYSAYSARKFFHFMIFLKEFSPSL
>NZ_CP033687.1|WP_035191149.1|3574545_3574725_-|hypothetical-protein
MSKKNQVFLVILLILSMTGFIIIMILDPVPPWLKAYNFLMVIAWGVWIYRTGKEKGHYW
>NZ_CP033687.1|WP_061577719.1|3575025_3575931_-|DMT-family-transporter
MNPYIALIAGVLAVTSSAILVKYSTADAGVIAFYRLFFTTIIMLPIFLAARKKAKMRMLKKDLLFSISSGALLAFHFILWFESLNLTSVASSTVLVTLQPVFAFAGSYFIFREPLSLKAIVCAAFSIFGSILISWGDFFISGKALYGDVLALISCLFVTAYMMIGQYVRKRADVVPYTFVVYLASTVVLFFYVLFAGEAFYPYSARNWICFLLLAVLPTLAGHSVFSWVVKWISASVVSVAILFEPVGAAILAYLLFGEKISWFQAVGGIIILLSIAYFLARDHAEHRRAVRLNEKSEPAR
>NZ_CP033687.1|WP_013860047.1|3576021_3576711_+|MgtC/SapB-family-protein
MVFGDLEILYKLGITAVLGLIIGLERELKRKPLGLKTSLVISIISCLLTIVSIQSAYLFNHAHSVQITMDPLRLAAQIVSGIGFLGAGVILKKDNDTITGLTTAAMIWGASGIGIAVGAGFYMEAIAGVVLIIISVEIIPYLMGKAVQTKLRNKDLIIKVIVRNRDAIPCVLDAIEKQQITIENIRIKDLKDQTHLVDLKARASYKHTTVDVYRHISGMDEVAAAEVES
>NZ_CP033687.1|WP_081106251.1|3576846_3577971_-|DUF1646-family-protein
MSRGGRLFCFPKKMKGSGLMVMGLTVILLLVLCLPFTKIVERNLEAFLFVMGVAACIVSRSFSWHLVQEALLHPLNITIAVLAMGLLFRWFEKPIEKGIRRISHAMPFRLFIALFVIILGLLSSVITAIVAAIILVAVIRFLRFDRKTEVRLVVLACFAIGLGAVLTPIGEPLSTIVVSKLDADFFYLLRLTGTSVIPAVIVFGVLAALIVKPGQYSSAMETAAGKEPGMATTEDGGLKAETASESYKEIVIRSFKIYLFVMALTLLGAGFEPFIEAYLLDLSPRVLYWINMVSAVLDNATLAAAEISPAMNDKAIQDILMGLLISGGMLVPGNIPNIIAAGKLKISSLEYARFAFPLGLAAMVVYFVIILFLV
>NZ_CP033687.1|WP_061565795.1|3578480_3578867_-|MFS-transporter
MNRIQRIKNTYYAFNILYNMGIMVFGGTLYLYMKSIHDSYADINLFLSIFWIVGFITEIPSSVIADTFGRKKTLISSCVIRSIGLFLLFFDWGNMVFLILSAIFTLLGESLRSGTVDSWMIDSIREEE

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP033687_3	3.66\|462874\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	462874-462907	34	NZ_CP033687.1	44527-44560	0	1.0
NZ_CP033687_3	3.20\|459849\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459849-459882	34	NZ_CP033687.1	46651-46684	1	0.971
NZ_CP033687_3	3.71\|463204\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463204-463236	33	NZ_CP033687.1	54484-54516	1	0.97
NZ_CP033687_3	3.82\|463927\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463927-463960	34	NZ_CP033687.1	9299-9332	1	0.971
NZ_CP033687_3	3.119\|466369\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466369-466401	33	NZ_CP033687.1	47382-47414	1	0.97
NZ_CP033687_12	12.1\|2469562\|19\|NZ_CP033687\|CRT	2469562-2469580	19	NZ_CP033687.1	1235414-1235432	1	0.947
NZ_CP033687_12	12.1\|2469562\|19\|NZ_CP033687\|CRT	2469562-2469580	19	NZ_CP033687.1	2467941-2467959	1	0.947
NZ_CP033687_12	12.1\|2469562\|19\|NZ_CP033687\|CRT	2469562-2469580	19	NZ_CP033687.1	2467993-2468011	1	0.947
NZ_CP033687_12	12.4\|2469718\|19\|NZ_CP033687\|CRT	2469718-2469736	19	NZ_CP033687.1	1235414-1235432	1	0.947
NZ_CP033687_12	12.4\|2469718\|19\|NZ_CP033687\|CRT	2469718-2469736	19	NZ_CP033687.1	2467941-2467959	1	0.947
NZ_CP033687_12	12.4\|2469718\|19\|NZ_CP033687\|CRT	2469718-2469736	19	NZ_CP033687.1	2467993-2468011	1	0.947
NZ_CP033687_12	12.9\|2469562\|27\|NZ_CP033687\|CRISPRCasFinder	2469562-2469588	27	NZ_CP033687.1	2467993-2468019	1	0.963
NZ_CP033687_12	12.12\|2469718\|27\|NZ_CP033687\|CRISPRCasFinder	2469718-2469744	27	NZ_CP033687.1	2467993-2468019	1	0.963
NZ_CP033687_7	7.2\|1603209\|19\|NZ_CP033687\|CRT	1603209-1603227	19	NZ_CP033687.1	1235467-1235485	2	0.895
NZ_CP033687_7	7.6\|1603417\|19\|NZ_CP033687\|CRT	1603417-1603435	19	NZ_CP033687.1	3102501-3102519	2	0.895
NZ_CP033687_12	12.1\|2469562\|19\|NZ_CP033687\|CRT	2469562-2469580	19	NZ_CP033687.1	1235674-1235692	2	0.895
NZ_CP033687_12	12.2\|2469614\|19\|NZ_CP033687\|CRT	2469614-2469632	19	NZ_CP033687.1	128266-128284	2	0.895
NZ_CP033687_12	12.2\|2469614\|19\|NZ_CP033687\|CRT	2469614-2469632	19	NZ_CP033687.1	1235622-1235640	2	0.895
NZ_CP033687_12	12.2\|2469614\|19\|NZ_CP033687\|CRT	2469614-2469632	19	NZ_CP033687.1	1235934-1235952	2	0.895
NZ_CP033687_12	12.2\|2469614\|19\|NZ_CP033687\|CRT	2469614-2469632	19	NZ_CP033687.1	2260431-2260449	2	0.895
NZ_CP033687_12	12.4\|2469718\|19\|NZ_CP033687\|CRT	2469718-2469736	19	NZ_CP033687.1	1235674-1235692	2	0.895
NZ_CP033687_12	12.9\|2469562\|27\|NZ_CP033687\|CRISPRCasFinder	2469562-2469588	27	NZ_CP033687.1	1235406-1235432	2	0.926
NZ_CP033687_12	12.10\|2469614\|27\|NZ_CP033687\|CRISPRCasFinder	2469614-2469640	27	NZ_CP033687.1	128258-128284	2	0.926
NZ_CP033687_12	12.10\|2469614\|27\|NZ_CP033687\|CRISPRCasFinder	2469614-2469640	27	NZ_CP033687.1	1235614-1235640	2	0.926
NZ_CP033687_12	12.12\|2469718\|27\|NZ_CP033687\|CRISPRCasFinder	2469718-2469744	27	NZ_CP033687.1	1235406-1235432	2	0.926

1. spacer 3.66|462874|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to position: 44527-44560, mismatch: 0, identity: 1.0

cattgaccgaattggtacattaaaaaatccaata	CRISPR spacer
cattgaccgaattggtacattaaaaaatccaata	Protospacer
**********************************

2. spacer 3.20|459849|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to position: 46651-46684, mismatch: 1, identity: 0.971

gcaagctaactaagaaaactaaatatggctccaa	CRISPR spacer
gcaagcaaactaagaaaactaaatatggctccaa	Protospacer
****** ***************************

3. spacer 3.71|463204|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to position: 54484-54516, mismatch: 1, identity: 0.97

ctgaatcctaacccatccgccatatactgaagt	CRISPR spacer
ctgaatcctaatccatccgccatatactgaagt	Protospacer
***********.*********************

4. spacer 3.82|463927|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to position: 9299-9332, mismatch: 1, identity: 0.971

gccactataagtcaaaaaatacgacatacaatgg	CRISPR spacer
gccactataagtcgaaaaatacgacatacaatgg	Protospacer
*************.********************

5. spacer 3.119|466369|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to position: 47382-47414, mismatch: 1, identity: 0.97

gcagatggggatcagcaaggcgataggatttat	CRISPR spacer
gcagatggggatcagcaaggcgattggatttat	Protospacer
************************ ********

6. spacer 12.1|2469562|19|NZ_CP033687|CRT matches to position: 1235414-1235432, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatccgggctcg	Protospacer
***********.*******

7. spacer 12.1|2469562|19|NZ_CP033687|CRT matches to position: 2467941-2467959, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatctgggcccg	Protospacer
****************.**

8. spacer 12.1|2469562|19|NZ_CP033687|CRT matches to position: 2467993-2468011, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatctggtctcg	Protospacer
************** ****

9. spacer 12.4|2469718|19|NZ_CP033687|CRT matches to position: 1235414-1235432, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatccgggctcg	Protospacer
***********.*******

10. spacer 12.4|2469718|19|NZ_CP033687|CRT matches to position: 2467941-2467959, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatctgggcccg	Protospacer
****************.**

11. spacer 12.4|2469718|19|NZ_CP033687|CRT matches to position: 2467993-2468011, mismatch: 1, identity: 0.947

caagctgtatctgggctcg	CRISPR spacer
caagctgtatctggtctcg	Protospacer
************** ****

12. spacer 12.9|2469562|27|NZ_CP033687|CRISPRCasFinder matches to position: 2467993-2468019, mismatch: 1, identity: 0.963

caagctgtatctgggctcggaatgtcc	CRISPR spacer
caagctgtatctggtctcggaatgtcc	Protospacer
************** ************

13. spacer 12.12|2469718|27|NZ_CP033687|CRISPRCasFinder matches to position: 2467993-2468019, mismatch: 1, identity: 0.963

caagctgtatctgggctcggaatgtcc	CRISPR spacer
caagctgtatctggtctcggaatgtcc	Protospacer
************** ************

14. spacer 7.2|1603209|19|NZ_CP033687|CRT matches to position: 1235467-1235485, mismatch: 2, identity: 0.895

gggcccggatgcagctcgt	CRISPR spacer
ggacccggatgcagcttgt	Protospacer
**.*************.**

15. spacer 7.6|1603417|19|NZ_CP033687|CRT matches to position: 3102501-3102519, mismatch: 2, identity: 0.895

attcccggatgcggcacgt	CRISPR spacer
attcccggatgccgaacgt	Protospacer
************ * ****

16. spacer 12.1|2469562|19|NZ_CP033687|CRT matches to position: 1235674-1235692, mismatch: 2, identity: 0.895

caagctgtatctgggctcg	CRISPR spacer
catgctgtatccgggctcg	Protospacer
** ********.*******

17. spacer 12.2|2469614|19|NZ_CP033687|CRT matches to position: 128266-128284, mismatch: 2, identity: 0.895

cacgttgcatccggtcccg	CRISPR spacer
cacgttgcatccgagcccg	Protospacer
*************. ****

18. spacer 12.2|2469614|19|NZ_CP033687|CRT matches to position: 1235622-1235640, mismatch: 2, identity: 0.895

cacgttgcatccggtcccg	CRISPR spacer
cacgttgcatcctggcccg	Protospacer
************ * ****

19. spacer 12.2|2469614|19|NZ_CP033687|CRT matches to position: 1235934-1235952, mismatch: 2, identity: 0.895

cacgttgcatccggtcccg	CRISPR spacer
cacgttgcatccgggctcg	Protospacer
************** *.**

20. spacer 12.2|2469614|19|NZ_CP033687|CRT matches to position: 2260431-2260449, mismatch: 2, identity: 0.895

cacgttgcatccggtcccg	CRISPR spacer
cacgctgcatccgggcccg	Protospacer
****.********* ****

21. spacer 12.4|2469718|19|NZ_CP033687|CRT matches to position: 1235674-1235692, mismatch: 2, identity: 0.895

caagctgtatctgggctcg	CRISPR spacer
catgctgtatccgggctcg	Protospacer
** ********.*******

22. spacer 12.9|2469562|27|NZ_CP033687|CRISPRCasFinder matches to position: 1235406-1235432, mismatch: 2, identity: 0.926

caagctgtatctgggctcggaatgtcc	CRISPR spacer
caagctgtatccgggctcgaaatgtcc	Protospacer
***********.*******.*******

23. spacer 12.10|2469614|27|NZ_CP033687|CRISPRCasFinder matches to position: 128258-128284, mismatch: 2, identity: 0.926

cacgttgcatccggtcccgaaatgtcc	CRISPR spacer
cacgttgcatccgagcccgaaatgtcc	Protospacer
*************. ************

24. spacer 12.10|2469614|27|NZ_CP033687|CRISPRCasFinder matches to position: 1235614-1235640, mismatch: 2, identity: 0.926

cacgttgcatccggtcccgaaatgtcc	CRISPR spacer
cacgttgcatcctggcccgaaatgtcc	Protospacer
************ * ************

25. spacer 12.12|2469718|27|NZ_CP033687|CRISPRCasFinder matches to position: 1235406-1235432, mismatch: 2, identity: 0.926

caagctgtatctgggctcggaatgtcc	CRISPR spacer
caagctgtatccgggctcgaaatgtcc	Protospacer
***********.*******.*******

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP033687_1	1.1\|237662\|24\|NZ_CP033687\|CRISPRCasFinder	237662-237685	24	NZ_AP023206	Escherichia coli strain TUM18781 plasmid pMTY18781-1_lncX3, complete sequence	26776-26799	2	0.917
NZ_CP033687_4	4.7\|469127\|34\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469127-469160	34	MF417903	Uncultured Caudovirales phage clone 10F_3, partial genome	4159-4192	4	0.882
NZ_CP033687_10	10.1\|2131683\|25\|NZ_CP033687\|CRISPRCasFinder	2131683-2131707	25	NZ_CP020539	Sphingobium herbicidovorans strain MH plasmid pMSHV, complete sequence	338428-338452	5	0.8
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_LR134399	Listeria monocytogenes strain NCTC7974 plasmid 2, complete sequence	57355-57409	6	0.891
NZ_CP033687_3	3.28\|460376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	460376-460409	34	NZ_CP025992	Lactobacillus plantarum subsp. plantarum strain LB1-2 plasmid pLB1-2A, complete sequence	105442-105475	7	0.794
NZ_CP033687_3	3.72\|463269\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463269-463302	34	MH593832	Phage sp. isolate ctcj9, complete genome	8526-8559	7	0.794
NZ_CP033687_3	3.95\|464781\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	464781-464813	33	NZ_CP017943	Phyllobacterium zundukense strain Tri-48 plasmid unnamed2, complete sequence	423304-423336	7	0.788
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP004876	Bacillus thuringiensis serovar kurstaki str. HD-1 plasmid pBMB299, complete sequence	218445-218478	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NC_017203	Bacillus thuringiensis serovar chinensis CT-43 plasmid pCT281, complete sequence	249523-249556	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NC_020384	Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-285, complete sequence	253752-253785	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP020005	Bacillus thuringiensis strain Bacillus thuringiensis L-7601 plasmid unnamed3, complete sequence	312293-312326	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP015177	Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB267, complete sequence	211574-211607	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP004861	Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB293, complete sequence	216880-216913	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP010091	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence	231072-231105	7	0.794
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	NZ_CP011350	Bacillus thuringiensis strain YC-10 plasmid pYC1, complete sequence	628846-628879	7	0.794
NZ_CP033687_3	3.119\|466369\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466369-466401	33	MN484601	Gordonia phage Sixama, complete genome	35547-35579	7	0.788
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP015440	Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_2, complete sequence	64784-64838	7	0.873
NZ_CP033687_3	3.4\|458793\|34\|NZ_CP033687\|CRT,PILER-CR,CRISPRCasFinder	458793-458826	34	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	583270-583303	8	0.765
NZ_CP033687_3	3.17\|459651\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459651-459684	34	MG757166	Gordonia phage SuperSulley, complete genome	8454-8487	8	0.765
NZ_CP033687_3	3.17\|459651\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459651-459684	34	MH779499	Gordonia phage Buggaboo, complete genome	8454-8487	8	0.765
NZ_CP033687_3	3.19\|459784\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459784-459816	33	NZ_CP015355	Bacillus thuringiensis strain MYBT18246 plasmid p109822, complete sequence	68670-68702	8	0.758
NZ_CP033687_3	3.22\|459981\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459981-460014	34	NC_001942	Mycoplasma phage MAV1, complete genome	7926-7959	8	0.765
NZ_CP033687_3	3.22\|459981\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459981-460014	34	AF074945	Mycoplasma arthritidis bacteriophage MAV1, complete genome	7926-7959	8	0.765
NZ_CP033687_3	3.39\|461101\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	461101-461133	33	NZ_CP013043	Clostridium perfringens strain JP55 plasmid pJFP55H, complete sequence	38180-38212	8	0.758
NZ_CP033687_3	3.80\|463795\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463795-463828	34	NC_014025	Bacillus megaterium QM B1551 plasmid pBM500, complete sequence	13747-13780	8	0.765
NZ_CP033687_3	3.101\|465180\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465180-465213	34	AP014353	Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S39-C37, * SEQUENCING IN PROGRESS *	26205-26238	8	0.765
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	305102-305135	8	0.765
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	62992-63025	8	0.765
NZ_CP033687_3	3.118\|466304\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466304-466336	33	NZ_CP030354	Novosphingobium sp. P6W plasmid pP6W1, complete sequence	655270-655302	8	0.758
NZ_CP033687_3	3.118\|466304\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466304-466336	33	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	433127-433159	8	0.758
NZ_CP033687_3	3.118\|466304\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466304-466336	33	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	465468-465500	8	0.758
NZ_CP033687_4	4.1\|468729\|34\|NZ_CP033687\|CRISPRCasFinder,CRT	468729-468762	34	GQ443085	Clostridium phage CP26F, complete genome	12376-12409	8	0.765
NZ_CP033687_4	4.1\|468729\|34\|NZ_CP033687\|CRISPRCasFinder,CRT	468729-468762	34	JF767210	Clostridium phage phi9O, complete genome	12781-12814	8	0.765
NZ_CP033687_4	4.1\|468729\|34\|NZ_CP033687\|CRISPRCasFinder,CRT	468729-468762	34	NC_019496	Clostridium phage phiCP26F, complete genome	12376-12409	8	0.765
NZ_CP033687_4	4.6\|469060\|35\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469060-469094	35	AP013390	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6-MedDCM-OCT-S27-C41	26930-26964	8	0.771
NZ_CP033687_4	4.6\|469060\|35\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469060-469094	35	AP013392	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S43-C64	2074-2108	8	0.771
NZ_CP033687_4	4.6\|469060\|35\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469060-469094	35	AP013391	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S33-C54	33239-33273	8	0.771
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP015439	Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_1, complete sequence	255881-255935	8	0.855
NZ_CP033687_3	3.4\|458793\|34\|NZ_CP033687\|CRT,PILER-CR,CRISPRCasFinder	458793-458826	34	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	219732-219765	9	0.735
NZ_CP033687_3	3.7\|458991\|34\|NZ_CP033687\|CRT,PILER-CR,CRISPRCasFinder	458991-459024	34	NZ_CP032530	Bacillus megaterium NCT-2 plasmid pNCT2_2, complete sequence	64506-64539	9	0.735
NZ_CP033687_3	3.118\|466304\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466304-466336	33	NC_009427	Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence	23029-23061	9	0.727
NZ_CP033687_3	3.121\|466501\|35\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466501-466535	35	KX879602	Liberibacter phage HHCA1-2, complete genome	1474-1508	9	0.743
NZ_CP033687_4	4.1\|468729\|34\|NZ_CP033687\|CRISPRCasFinder,CRT	468729-468762	34	MK448365	Streptococcus satellite phage Javan212, complete genome	2507-2540	9	0.735
NZ_CP033687_4	4.6\|469060\|35\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469060-469094	35	MN694669	Marine virus AFVG_250M354, complete genome	6329-6363	9	0.743
NZ_CP033687_4	4.9\|469259\|34\|NZ_CP033687\|CRISPRCasFinder,CRT,PILER-CR	469259-469292	34	NZ_CP015507	Bacillus oceanisediminis 2691 plasmid pBO1, complete sequence	352644-352677	9	0.735
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP024037	Bacillus aryabhattai strain K13 plasmid unnamed2	10428-10482	9	0.836
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP026740	Bacillus megaterium strain YC4-R4 plasmid unnamed4	70775-70829	9	0.836
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP010587	Bacillus megaterium Q3 plasmid p1, complete sequence	832-886	9	0.836
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP023319	Bacillus megaterium strain A plasmid p2, complete sequence	75819-75873	9	0.836
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NC_017139	Bacillus megaterium WSH-002 plasmid WSH-002_p1, complete sequence	1329-1383	9	0.836
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NC_020451	Vibrio coralliilyticus strain ATCC BAA-450 plasmid, complete sequence	1971-2025	9	0.836
NZ_CP033687_3	3.16\|459585\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	459585-459618	34	NC_048753	Lactobacillus phage 3-521, complete genome	61770-61803	10	0.706
NZ_CP033687_3	3.70\|463138\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463138-463171	34	MK017819	Clostridium phage CPD4, complete genome	40602-40635	10	0.706
NZ_CP033687_3	3.71\|463204\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463204-463236	33	NC_007410	Trichormus variabilis ATCC 29413 plasmid A, complete sequence	154703-154735	10	0.697
NZ_CP033687_3	3.71\|463204\|33\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	463204-463236	33	NZ_CP047243	Trichormus variabilis 0441 plasmid unnamed1, complete sequence	160428-160460	10	0.697
NZ_CP033687_3	3.86\|464188\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	464188-464221	34	NC_019728	Calothrix sp. PCC 6303 plasmid pCAL6303.02, complete sequence	39358-39391	10	0.706
NZ_CP033687_3	3.90\|464452\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	464452-464485	34	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	616419-616452	10	0.706
NZ_CP033687_3	3.90\|464452\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	464452-464485	34	MN694585	Marine virus AFVG_250M655, complete genome	16674-16707	10	0.706
NZ_CP033687_3	3.99\|465045\|35\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465045-465079	35	NZ_CP040097	Pantoea sp. SO10 plasmid unnamed2, complete sequence	60481-60515	10	0.714
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	MT679222	Proteus phage 2, complete genome	92186-92219	10	0.706
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	MT679223	Proteus phage 1, complete genome	92443-92476	10	0.706
NZ_CP033687_3	3.104\|465376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465376-465409	34	MT740245	Proteus phage M4H10_20, complete genome	92566-92599	10	0.706
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	405090-405123	10	0.706
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	404358-404391	10	0.706
NZ_CP033687_3	3.121\|466501\|35\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466501-466535	35	KX879602	Liberibacter phage HHCA1-2, complete genome	37575-37609	10	0.714
NZ_CP033687_3	3.121\|466501\|35\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466501-466535	35	JF773396	Liberibacter phage FP2, complete genome	3769-3803	10	0.714
NZ_CP033687_3	3.121\|466501\|35\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	466501-466535	35	NC_019550	Liberibacter phage SC2, complete genome	37583-37617	10	0.714
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NC_048753	Lactobacillus phage 3-521, complete genome	13549-13603	10	0.818
NZ_CP033687_3	3.23\|460047\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	460047-460080	34	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	125674-125707	11	0.676
NZ_CP033687_3	3.23\|460047\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	460047-460080	34	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	122853-122886	11	0.676
NZ_CP033687_3	3.28\|460376\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	460376-460409	34	NZ_LR214986	Mycoplasma cynos strain NCTC10142 plasmid 13	252847-252880	11	0.676
NZ_CP033687_3	3.90\|464452\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	464452-464485	34	MG592553	Vibrio phage 1.187.O._10N.286.49.F1, partial genome	39294-39327	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	345896-345929	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	621279-621312	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	761343-761376	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP049158	Caballeronia sp. SBC1 plasmid pSBC1_2, complete sequence	96380-96413	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP049318	Caballeronia sp. SBC2 plasmid pSBC2-2, complete sequence	96326-96359	11	0.676
NZ_CP033687_3	3.110\|465772\|34\|NZ_CP033687\|CRT,CRISPRCasFinder,PILER-CR	465772-465805	34	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	427324-427357	11	0.676
NZ_CP033687_14	14.1\|3560120\|55\|NZ_CP033687\|CRISPRCasFinder	3560120-3560174	55	NZ_CP033045	Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence	483785-483839	11	0.8

1. spacer 1.1|237662|24|NZ_CP033687|CRISPRCasFinder matches to NZ_AP023206 (Escherichia coli strain TUM18781 plasmid pMTY18781-1_lncX3, complete sequence) position: , mismatch: 2, identity: 0.917

ccttcttccttccccttttcaatc	CRISPR spacer
ccttcttctttccccttttccatc	Protospacer
********.*********** ***

2. spacer 4.7|469127|34|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to MF417903 (Uncultured Caudovirales phage clone 10F_3, partial genome) position: , mismatch: 4, identity: 0.882

actccacaactttgaggagtcaacttacaccaac	CRISPR spacer
actccacaactttgtggagtcaacttacgaaaac	Protospacer
************** *************.  ***

3. spacer 10.1|2131683|25|NZ_CP033687|CRISPRCasFinder matches to NZ_CP020539 (Sphingobium herbicidovorans strain MH plasmid pMSHV, complete sequence) position: , mismatch: 5, identity: 0.8

agtattttgtccttcatccccttgg	CRISPR spacer
tcgatgttgtccttcatccccttgt	Protospacer
   ** ******************

4. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_LR134399 (Listeria monocytogenes strain NCTC7974 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.891

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacaacagcttggaaggctgtagttttaccactaaactacacccgcatagtaag	Protospacer
**********************.*************************  . *.*

5. spacer 3.28|460376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP025992 (Lactobacillus plantarum subsp. plantarum strain LB1-2 plasmid pLB1-2A, complete sequence) position: , mismatch: 7, identity: 0.794

-gatgaatttacaaaaattatttgctgcacaagct	CRISPR spacer
tgatg-atttacaaaaattcttagctgcacataac	Protospacer
 **** ************* ** ******** . .

6. spacer 3.72|463269|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MH593832 (Phage sp. isolate ctcj9, complete genome) position: , mismatch: 7, identity: 0.794

gtagatcaagttctagcacaacgaggcattcaac	CRISPR spacer
gtagatcaagtactagcagaacgaggcaagcgct	Protospacer
*********** ****** *********  *. .

7. spacer 3.95|464781|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP017943 (Phyllobacterium zundukense strain Tri-48 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.788

gctttctatttcatttagatacgacacgccacc----	CRISPR spacer
gctttctatttcgttttgatacgaaa----acctcag	Protospacer
************.*** ******* *    ***

8. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP004876 (Bacillus thuringiensis serovar kurstaki str. HD-1 plasmid pBMB299, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

9. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_017203 (Bacillus thuringiensis serovar chinensis CT-43 plasmid pCT281, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

10. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_020384 (Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-285, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

11. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP020005 (Bacillus thuringiensis strain Bacillus thuringiensis L-7601 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

12. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP015177 (Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB267, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

13. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP004861 (Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB293, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

14. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP010091 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

15. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP011350 (Bacillus thuringiensis strain YC-10 plasmid pYC1, complete sequence) position: , mismatch: 7, identity: 0.794

aagtaaatttgatgatattgtgacaaa-tatcatg	CRISPR spacer
gcataaatttgatgttattctgacaaattatcaa-	Protospacer
. .*********** **** ******* *****

16. spacer 3.119|466369|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MN484601 (Gordonia phage Sixama, complete genome) position: , mismatch: 7, identity: 0.788

gcagatggggatcagcaaggcgata--ggatttat	CRISPR spacer
gcagatggcgatcagcaagacgatatcgagctt--	Protospacer
******** **********.*****  *...**

17. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP015440 (Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_2, complete sequence) position: , mismatch: 7, identity: 0.873

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcataataat	Protospacer
***** *************** **************************  * *.

18. spacer 3.4|458793|34|NZ_CP033687|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 8, identity: 0.765

ttgaccggggctgacggcggagctggattacacg	CRISPR spacer
gtgggaggggctgacggcggagctggacttcaac	Protospacer
 **.  *********************.* **

19. spacer 3.17|459651|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MG757166 (Gordonia phage SuperSulley, complete genome) position: , mismatch: 8, identity: 0.765

tgccggatat-----tcctggtgctttcggatccataat	CRISPR spacer
-----gagatctcgctcctggggctttcggatccagaat	Protospacer
     ** **     ****** ************* ***

20. spacer 3.17|459651|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MH779499 (Gordonia phage Buggaboo, complete genome) position: , mismatch: 8, identity: 0.765

tgccggatat-----tcctggtgctttcggatccataat	CRISPR spacer
-----gagatctcgctcctggggctttcggatccagaat	Protospacer
     ** **     ****** ************* ***

21. spacer 3.19|459784|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP015355 (Bacillus thuringiensis strain MYBT18246 plasmid p109822, complete sequence) position: , mismatch: 8, identity: 0.758

gacaaaatcgtcagctacgttttcgggcataga	CRISPR spacer
aacaaactcgtccgctacgttttcgtgtacaag	Protospacer
.***** ***** ************ *.*.*..

22. spacer 3.22|459981|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_001942 (Mycoplasma phage MAV1, complete genome) position: , mismatch: 8, identity: 0.765

gcgatatgttttcaaaagtaaaatcttttagctc---	CRISPR spacer
gtgtgatgttttctaaaataaaatctttt---tcaag	Protospacer
*.*  ******** ***.***********   **

23. spacer 3.22|459981|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to AF074945 (Mycoplasma arthritidis bacteriophage MAV1, complete genome) position: , mismatch: 8, identity: 0.765

gcgatatgttttcaaaagtaaaatcttttagctc---	CRISPR spacer
gtgtgatgttttctaaaataaaatctttt---tcaag	Protospacer
*.*  ******** ***.***********   **

24. spacer 3.39|461101|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP013043 (Clostridium perfringens strain JP55 plasmid pJFP55H, complete sequence) position: , mismatch: 8, identity: 0.758

attgcaaaatatagatattactcactgcaaacg	CRISPR spacer
tatgcaaactatagaaattactcactctaacag	Protospacer
  ****** ****** ********** .**  *

25. spacer 3.80|463795|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_014025 (Bacillus megaterium QM B1551 plasmid pBM500, complete sequence) position: , mismatch: 8, identity: 0.765

ctattacacaagcacagaaagctattagaatagc	CRISPR spacer
ctattacacaaggacataaagctattatctctgt	Protospacer
************ *** **********   . *.

26. spacer 3.101|465180|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to AP014353 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S39-C37, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 8, identity: 0.765

ctggctcgatcagcttacaaatcaatttagcgca	CRISPR spacer
gcgactcgatcatcttgcaaatcaattttacgaa	Protospacer
 .*.******** ***.*********** .** *

27. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 8, identity: 0.765

acggcaggcggtcgtcgaagtcgag-ccctggacg	CRISPR spacer
cggtcagccggtcgtagaagtcgagccccttggc-	Protospacer
  * *** ******* ********* **** *.*

28. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.765

acggcaggcggtcgtcgaagtcgag-ccctggacg	CRISPR spacer
cggtcagccggtcgtagaagtcgagccccttggc-	Protospacer
  * *** ******* ********* **** *.*

29. spacer 3.118|466304|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP030354 (Novosphingobium sp. P6W plasmid pP6W1, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgaggtcggcgtgattgtcgataacaccgcg	CRISPR spacer
ggcgagttcggcgtgatcgtcgatgccgtgccg	Protospacer
****** **********.******. *..  **

30. spacer 3.118|466304|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgaggtcggcgtgattgtcgataacaccgcg	CRISPR spacer
ggcgagttcggcgtgatcgtcgatgccgtgccg	Protospacer
****** **********.******. *..  **

31. spacer 3.118|466304|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgaggtcggcgtgattgtcgataacaccgcg	CRISPR spacer
ggcgagttcggcgtgatcgtcgatgccgtgccg	Protospacer
****** **********.******. *..  **

32. spacer 4.1|468729|34|NZ_CP033687|CRISPRCasFinder,CRT matches to GQ443085 (Clostridium phage CP26F, complete genome) position: , mismatch: 8, identity: 0.765

tcgtataattttttgttttaaatacaccattttt	CRISPR spacer
gattagcgttttttggtttaaatactccattttt	Protospacer
   **  .******* ********* ********

33. spacer 4.1|468729|34|NZ_CP033687|CRISPRCasFinder,CRT matches to JF767210 (Clostridium phage phi9O, complete genome) position: , mismatch: 8, identity: 0.765

tcgtataattttttgttttaaatacaccattttt	CRISPR spacer
gattagcgttttttggtttaaatactccattttt	Protospacer
   **  .******* ********* ********

34. spacer 4.1|468729|34|NZ_CP033687|CRISPRCasFinder,CRT matches to NC_019496 (Clostridium phage phiCP26F, complete genome) position: , mismatch: 8, identity: 0.765

tcgtataattttttgttttaaatacaccattttt	CRISPR spacer
gattagcgttttttggtttaaatactccattttt	Protospacer
   **  .******* ********* ********

35. spacer 4.6|469060|35|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to AP013390 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6-MedDCM-OCT-S27-C41) position: , mismatch: 8, identity: 0.771

cgacaccaattaaatctgcaacatatccttgagtc---	CRISPR spacer
ctacaccaattaaatctgcaacctgtct---agttact	Protospacer
* ******************** *.**.   ***.

36. spacer 4.6|469060|35|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to AP013392 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S43-C64) position: , mismatch: 8, identity: 0.771

cgacaccaattaaatctgcaacatatccttgagtc---	CRISPR spacer
ctacaccaattaaatctgcaacctgtct---agttact	Protospacer
* ******************** *.**.   ***.

37. spacer 4.6|469060|35|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to AP013391 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S33-C54) position: , mismatch: 8, identity: 0.771

cgacaccaattaaatctgcaacatatccttgagtc---	CRISPR spacer
ctacaccaattaaatctgcaacctgtct---agttact	Protospacer
* ******************** *.**.   ***.

38. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP015439 (Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_1, complete sequence) position: , mismatch: 8, identity: 0.855

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatattata	Protospacer
***** *************** **************************    * .

39. spacer 3.4|458793|34|NZ_CP033687|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.735

ttgaccggggctgacggcggagctggattacacg-	CRISPR spacer
cagaccggggctgacggcggagc-gggcgacggac	Protospacer
. ********************* **.. **. .

40. spacer 3.7|458991|34|NZ_CP033687|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP032530 (Bacillus megaterium NCT-2 plasmid pNCT2_2, complete sequence) position: , mismatch: 9, identity: 0.735

---gtttgatgctagaaatatttcatctgattttgtt	CRISPR spacer
aaaatt---ttttaaaaatatttcatctaattttgta	Protospacer
   .**   * .**.*************.*******

41. spacer 3.118|466304|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_009427 (Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence) position: , mismatch: 9, identity: 0.727

ggcgaggtcggcgtgattgtcgataacaccgcg	CRISPR spacer
ggcgagttcggcgtgatcgtcgatgcggtgccg	Protospacer
****** **********.******.  ..  **

42. spacer 3.121|466501|35|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to KX879602 (Liberibacter phage HHCA1-2, complete genome) position: , mismatch: 9, identity: 0.743

ttttttgctcaagctcatcaattcttttctcaaga	CRISPR spacer
caatttgttcaagatcatcaattcttttctgcaat	Protospacer
.  ****.***** ****************  *.

43. spacer 4.1|468729|34|NZ_CP033687|CRISPRCasFinder,CRT matches to MK448365 (Streptococcus satellite phage Javan212, complete genome) position: , mismatch: 9, identity: 0.735

tcgtataattttttgttttaaatacaccattttt	CRISPR spacer
acttgctcctttctgtttaaaatacaccattttt	Protospacer
 * *..  .***.***** ***************

44. spacer 4.6|469060|35|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to MN694669 (Marine virus AFVG_250M354, complete genome) position: , mismatch: 9, identity: 0.743

cgacaccaattaaatctgcaacatatccttgagtc	CRISPR spacer
ctacaccaattaaatcttctacatatcttcctgca	Protospacer
* *************** * *******.*.  *.

45. spacer 4.9|469259|34|NZ_CP033687|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015507 (Bacillus oceanisediminis 2691 plasmid pBO1, complete sequence) position: , mismatch: 9, identity: 0.735

ttttccatctataaaaaacgttccatttcataag	CRISPR spacer
cctggtattgataaaaaatgatccatttcataag	Protospacer
..*  .**. ********.* *************

46. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP024037 (Bacillus aryabhattai strain K13 plasmid unnamed2) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatatttta	Protospacer
***** *************** **************************      .

47. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP026740 (Bacillus megaterium strain YC4-R4 plasmid unnamed4) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatatttta	Protospacer
***** *************** **************************      .

48. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP010587 (Bacillus megaterium Q3 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatatttta	Protospacer
***** *************** **************************      .

49. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP023319 (Bacillus megaterium strain A plasmid p2, complete sequence) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatatttta	Protospacer
***** *************** **************************      .

50. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NC_017139 (Bacillus megaterium WSH-002 plasmid WSH-002_p1, complete sequence) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
cgacatcagcttggaaggctgaggttttaccactaaactacacccgcatatttta	Protospacer
***** *************** **************************      .

51. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NC_020451 (Vibrio coralliilyticus strain ATCC BAA-450 plasmid, complete sequence) position: , mismatch: 9, identity: 0.836

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
catcatcagcttggaaggctgaggttttaccactaaactacacccgcattttagt	Protospacer
*. ** *************** ************************** .  **

52. spacer 3.16|459585|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_048753 (Lactobacillus phage 3-521, complete genome) position: , mismatch: 10, identity: 0.706

atcgctctttcattagggcgaacagtgctttgtt	CRISPR spacer
atgcagctttaattaaggcgaacagtgcttatga	Protospacer
**    **** ****.**************

53. spacer 3.70|463138|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MK017819 (Clostridium phage CPD4, complete genome) position: , mismatch: 10, identity: 0.706

gtattaaaccaggattcccattcttgttgatatt	CRISPR spacer
ttactaaaccaggattctcattcttaagtttaac	Protospacer
 **.*************.*******.    ** .

54. spacer 3.71|463204|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_007410 (Trichormus variabilis ATCC 29413 plasmid A, complete sequence) position: , mismatch: 10, identity: 0.697

ctgaatcctaacccatccgccatatactgaagt	CRISPR spacer
aaataaaataacccatccgccagatactaaagc	Protospacer
  . *   ************** *****.***.

55. spacer 3.71|463204|33|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP047243 (Trichormus variabilis 0441 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

ctgaatcctaacccatccgccatatactgaagt	CRISPR spacer
aaataaaataacccatccgccagatactaaagc	Protospacer
  . *   ************** *****.***.

56. spacer 3.86|464188|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_019728 (Calothrix sp. PCC 6303 plasmid pCAL6303.02, complete sequence) position: , mismatch: 10, identity: 0.706

gagagaggcatttattttaaagtacatgggagag	CRISPR spacer
acttgggcaatttattttaaagtacctgcgagaa	Protospacer
.   *.*  **************** ** ****.

57. spacer 3.90|464452|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 10, identity: 0.706

tttggctggggatgatgttgtagagattgatggt	CRISPR spacer
gcggaaagccgatcatgttgtagaggttgatggt	Protospacer
 . *.  *  *** ***********.********

58. spacer 3.90|464452|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MN694585 (Marine virus AFVG_250M655, complete genome) position: , mismatch: 10, identity: 0.706

tttggctggg---gatgatgttgtagagattgatggt	CRISPR spacer
---gatcagacctgatgctgtcgtagagattgatggt	Protospacer
   *....*.   **** ***.***************

59. spacer 3.99|465045|35|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP040097 (Pantoea sp. SO10 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.714

acgaacaggcggacattttgcgccgcagtccgctg	CRISPR spacer
gatcccatcgggatattttgcgccgcagtctgctg	Protospacer
.    **   ***.****************.****

60. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MT679222 (Proteus phage 2, complete genome) position: , mismatch: 10, identity: 0.706

aagtaaatttgatgatattgtgacaaatatcatg	CRISPR spacer
tttcaaatttgatgatattgtggcaagtattgaa	Protospacer
   .******************.***.***.. .

61. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MT679223 (Proteus phage 1, complete genome) position: , mismatch: 10, identity: 0.706

aagtaaatttgatgatattgtgacaaatatcatg	CRISPR spacer
tttcaaatttgatgatattgtggcaagtattgaa	Protospacer
   .******************.***.***.. .

62. spacer 3.104|465376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MT740245 (Proteus phage M4H10_20, complete genome) position: , mismatch: 10, identity: 0.706

aagtaaatttgatgatattgtgacaaatatcatg	CRISPR spacer
tttcaaatttgatgatattgtggcaagtattgaa	Protospacer
   .******************.***.***.. .

63. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 10, identity: 0.706

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagccctgcctc	Protospacer
  . *********** ****** *******  .

64. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 10, identity: 0.706

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagcccggcccc	Protospacer
  . *********** ****** ***** *  *

65. spacer 3.121|466501|35|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to KX879602 (Liberibacter phage HHCA1-2, complete genome) position: , mismatch: 10, identity: 0.714

ttttttgctcaagctcatcaattcttttctcaaga	CRISPR spacer
acctctgttcaagatcatcaattcttttctgcaat	Protospacer
 ..*.**.***** ****************  *.

66. spacer 3.121|466501|35|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to JF773396 (Liberibacter phage FP2, complete genome) position: , mismatch: 10, identity: 0.714

ttttttgctcaagctcatcaattcttttctcaaga	CRISPR spacer
acctctgttcaagatcatcaattcttttctgcaat	Protospacer
 ..*.**.***** ****************  *.

67. spacer 3.121|466501|35|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_019550 (Liberibacter phage SC2, complete genome) position: , mismatch: 10, identity: 0.714

ttttttgctcaagctcatcaattcttttctcaaga	CRISPR spacer
acctctgttcaagatcatcaattcttttctgcaat	Protospacer
 ..*.**.***** ****************  *.

68. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NC_048753 (Lactobacillus phage 3-521, complete genome) position: , mismatch: 10, identity: 0.818

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
catctacagcttggaaggctgtggttttaccactaaactatacccgcgtgaacta	Protospacer
*. * ***********************************.******.  **  .

69. spacer 3.23|460047|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 11, identity: 0.676

tgcacagcaggagcgggaccggatcgatgcctgg	CRISPR spacer
gatacagcagcagcggcaccggatcgaagatcac	Protospacer
 ..******* ***** ********** * ...

70. spacer 3.23|460047|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 11, identity: 0.676

tgcacagcaggagcgggaccggatcgatgcctgg	CRISPR spacer
cttcaggcaggagcaggaccggattgatgctcga	Protospacer
. .  .********.*********.*****..*.

71. spacer 3.28|460376|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_LR214986 (Mycoplasma cynos strain NCTC10142 plasmid 13) position: , mismatch: 11, identity: 0.676

gatgaatttacaaaaattatttgctgcacaagct	CRISPR spacer
atagaatttagaaaaattattttctgcttatttc	Protospacer
.  ******* *********** **** .*  ..

72. spacer 3.90|464452|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to MG592553 (Vibrio phage 1.187.O._10N.286.49.F1, partial genome) position: , mismatch: 11, identity: 0.676

tttggctggggatgatgttgtagagattgatggt	CRISPR spacer
aattctctacgataatgtggtagagattgatggt	Protospacer
  *  .. . ***.**** ***************

73. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagcccggcctc	Protospacer
  . *********** ****** ***** *  .

74. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagcccggcctc	Protospacer
  . *********** ****** ***** *  .

75. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagcccggcctc	Protospacer
  . *********** ****** ***** *  .

76. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP049158 (Caballeronia sp. SBC1 plasmid pSBC1_2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
taagcaggcggtcgtcgaaatcgatccggccatt	Protospacer
  .****************.**** **    *.

77. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP049318 (Caballeronia sp. SBC2 plasmid pSBC2-2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
taagcaggcggtcgtcgaaatcgatccggccatt	Protospacer
  .****************.**** **    *.

78. spacer 3.110|465772|34|NZ_CP033687|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 11, identity: 0.676

acggcaggcggtcgtcgaagtcgagccctggacg	CRISPR spacer
cgatcaggcggtcgtagaagtccagcccggcctc	Protospacer
  . *********** ****** ***** *  .

79. spacer 14.1|3560120|55|NZ_CP033687|CRISPRCasFinder matches to NZ_CP033045 (Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.8

cgacaacagcttggaaggctgtggttttaccactaaactacacccgcagcaaagg	CRISPR spacer
catcatcagcttggaaggctgaggttttaccactaaactacacccgcatggttaa	Protospacer
*. ** *************** **************************  .  ..

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

19294 : 60670

Listeria_phage(17.65%)

tail,portal,terminase,integrase,capsid

attL 10818:10833|attR 62300:62315

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
10818:10833	attL	NA	NA	NA	NA
WP_110134071.1\|19294_21778_-	hypothetical protein	A0A2P0ZLF8	Lactobacillus_phage	6.1e-49	30.0
WP_110134072.1\|21791_23474_-\|tail	phage tail protein	A0A059T682	Listeria_phage	1.9e-81	33.6
WP_110134073.1\|23470_27514_-	tape measure protein	Q8LTK2	Lactococcus_phage	6.9e-66	45.9
WP_029142825.1\|27510_28128_-	hypothetical protein	O03936	Lactobacillus_phage	4.6e-30	40.4
WP_029142824.1\|28134_28560_-	hypothetical protein	NA	NA	NA	NA
WP_110134074.1\|28612_29083_-\|capsid	capsid protein	O03972	Lactobacillus_phage	1.5e-44	61.1
WP_110134075.1\|29088_29574_-	hypothetical protein	NA	NA	NA	NA
WP_029142848.1\|29494_29848_-	hypothetical protein	A0A1B1P872	Bacillus_phage	2.9e-29	53.1
WP_035176647.1\|29852_30203_-	hypothetical protein	NA	NA	NA	NA
WP_110134076.1\|30269_30653_-	hypothetical protein	NA	NA	NA	NA
WP_029142851.1\|30655_30892_-	hypothetical protein	B5LPR5	Bacillus_virus	7.4e-13	46.8
WP_110134077.1\|30925_31855_-\|capsid	capsid protein	A0A1B1P885	Bacillus_phage	3.9e-105	62.7
WP_029142853.1\|31867_32539_-	hypothetical protein	M9Q248	Clostridium_phage	1.9e-05	34.8
WP_110134078.1\|32635_32893_-	hypothetical protein	A0A1S5SBT9	Streptococcus_phage	1.2e-19	57.6
WP_110134079.1\|32946_34056_-\|capsid	minor capsid protein	B5LPR2	Bacillus_virus	2.8e-86	43.8
WP_110134080.1\|34059_35586_-\|portal	phage portal protein	A0A1B1P863	Bacillus_phage	3.1e-136	53.7
WP_110134081.1\|35598_36891_-\|terminase	PBSX family phage terminase large subunit	A0A1B1P869	Bacillus_phage	4.6e-197	76.6
WP_110134082.1\|36859_37627_-	hypothetical protein	A0A2P1JTW4	Anoxybacillus_phage	9.4e-65	59.6
WP_046721464.1\|37700_37904_-	hypothetical protein	NA	NA	NA	NA
WP_110134306.1\|38168_38546_-	helix-turn-helix domain-containing protein	A0A290FZR5	Caldibacillus_phage	4.5e-28	50.8
WP_110134083.1\|38611_39136_-	hypothetical protein	A0A0F7ILJ3	Polaribacter_phage	1.3e-25	43.3
WP_110134084.1\|39149_39335_-	hypothetical protein	NA	NA	NA	NA
WP_110134085.1\|39419_39665_-	hypothetical protein	NA	NA	NA	NA
WP_110134086.1\|39695_40472_-	phosphoadenosine phosphosulfate reductase family protein	NA	NA	NA	NA
WP_110134087.1\|40413_41130_-	CRISPR system precrRNA processing endoribonuclease RAMP protein Cas6	NA	NA	NA	NA
WP_110134088.1\|41122_41806_-	hypothetical protein	NA	NA	NA	NA
WP_110134089.1\|41802_42759_-	hypothetical protein	A0A0N7CDP5	Skermania_phage	4.2e-22	32.1
WP_110134090.1\|42760_42991_-	hypothetical protein	NA	NA	NA	NA
WP_142010178.1\|43059_43845_-	hypothetical protein	NA	NA	NA	NA
WP_110134092.1\|43936_44407_-	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_110134307.1\|45100_45274_-	DUF3954 domain-containing protein	NA	NA	NA	NA
WP_110134093.1\|45374_45761_-	hypothetical protein	H7BVT3	unidentified_phage	1.3e-11	37.2
WP_110134094.1\|46253_46715_-	DUF1064 domain-containing protein	A0A2P1JTY5	Anoxybacillus_phage	2.5e-57	79.3
WP_110134095.1\|46724_47288_-	dUTPase	R9TQ23	Paenibacillus_phage	3.0e-36	48.9
WP_110134096.1\|47284_47482_-	hypothetical protein	NA	NA	NA	NA
WP_110134097.1\|47643_47823_-	hypothetical protein	NA	NA	NA	NA
WP_110134098.1\|47822_48689_-	ATP-binding protein	S6B1M2	Thermus_phage	3.2e-114	72.2
WP_110134099.1\|48612_49428_-	hypothetical protein	A0A1C8E9B4	Bacillus_phage	3.5e-25	58.3
WP_110134100.1\|49483_50377_-	recombinase RecT	A8ATY6	Listeria_phage	7.3e-93	67.8
WP_110134308.1\|50376_51318_-	hypothetical protein	A8ATY5	Listeria_phage	2.6e-109	62.9
WP_110134101.1\|51420_51633_-	hypothetical protein	A0A290GDU5	Caldibacillus_phage	1.4e-07	42.0
WP_029142711.1\|51625_51865_-	hypothetical protein	NA	NA	NA	NA
WP_029142709.1\|52487_52772_-	hypothetical protein	NA	NA	NA	NA
WP_029142708.1\|52771_53290_-	hypothetical protein	A0A290FZK9	Caldibacillus_phage	3.7e-25	40.5
WP_035176495.1\|53350_53536_-	helix-turn-helix domain-containing protein	U5P0W4	Brevibacillus_phage	1.0e-09	61.8
WP_029142707.1\|53537_54329_-	hypothetical protein	A8ATY0	Listeria_phage	4.8e-56	45.0
WP_029142706.1\|54329_54572_-	helix-turn-helix transcriptional regulator	A8ATX6	Listeria_phage	2.1e-15	54.2
WP_029142705.1\|54736_55141_+	helix-turn-helix transcriptional regulator	A8ATX5	Listeria_phage	9.4e-08	46.8
WP_029142704.1\|55164_55791_+	ImmA/IrrE family metallo-endopeptidase	A0A1L2JY13	Aeribacillus_phage	5.7e-20	34.7
WP_052472245.1\|55828_56764_+	outer membrane protein assembly factor BamE	NA	NA	NA	NA
WP_110134102.1\|56809_58039_+	endonuclease	A0A1P8CWK6	Bacillus_phage	2.6e-64	70.4
WP_110134103.1\|58144_59374_+\|integrase	site-specific integrase	A0A0K2CZ62	Paenibacillus_phage	1.3e-92	43.4
WP_014097579.1\|59668_60670_+	potassium channel protein	A0A1B0Y2S3	Lactobacillus_phage	2.9e-05	50.0
62300:62315	attR	NA	NA	NA	NA

DBSCAN-SWA_2

780949 : 789262

Synechococcus_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_035190016.1\|780949_781543_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	3.2e-28	39.8
WP_110134241.1\|781535_782579_-	phosphoribosylformylglycinamidine cyclo-ligase	A0A0E3F760	Synechococcus_phage	5.0e-61	42.1
WP_017550745.1\|782598_784023_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	7.9e-49	33.7
WP_110134242.1\|784007_786257_-	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	3.5e-168	44.2
WP_110134243.1\|786240_786924_-	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_013860601.1\|786920_787175_-	phosphoribosylformylglycinamidine synthase subunit PurS	NA	NA	NA	NA
WP_110134244.1\|787167_787878_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A1D7SS43	Cyanophage	1.5e-48	43.7
WP_026684439.1\|787966_789262_-	adenylosuccinate lyase	A0A1B3B081	Gordonia_phage	6.5e-18	32.8

DBSCAN-SWA_3

978862 : 1027591

Indivirus(16.67%)

tRNA,protease,bacteriocin,transposase,coat

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_013858128.1\|978862_980173_-\|transposase	transposase	NA	NA	NA	NA
WP_014096740.1\|980464_981610_-	hypothetical protein	NA	NA	NA	NA
WP_061577323.1\|981622_982456_-	hypothetical protein	NA	NA	NA	NA
WP_014096738.1\|982452_983142_-	ABC transporter ATP-binding protein	A0A1V0SE00	Indivirus	4.2e-08	24.2
WP_014096737.1\|983138_983540_-	GntR family transcriptional regulator	NA	NA	NA	NA
WP_014096736.1\|983810_985412_-	CTP synthase	A0A1J0FA14	Only_Syngen_Nebraska_virus	1.0e-150	51.4
WP_014096735.1\|985642_986227_-	DNA-directed RNA polymerase subunit delta	NA	NA	NA	NA
WP_017550321.1\|986342_986549_-	hypothetical protein	NA	NA	NA	NA
WP_014096734.1\|987238_987919_+	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	8.1e-28	33.5
WP_104851084.1\|990343_992029_+\|transposase	IS1634 family transposase	NA	NA	NA	NA
WP_110134265.1\|992592_995847_-	methylmalonyl-CoA mutase	NA	NA	NA	NA
WP_017550324.1\|995932_996568_-	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_035183210.1\|996587_997730_-	acyl-CoA dehydrogenase	NA	NA	NA	NA
WP_013860764.1\|997763_998900_-	acyl-CoA dehydrogenase	NA	NA	NA	NA
WP_035183208.1\|998941_1000120_-	acetyl-CoA C-acetyltransferase	NA	NA	NA	NA
WP_035190064.1\|1000847_1002992_-	4Fe-4S dicluster domain-containing protein	NA	NA	NA	NA
WP_035190066.1\|1003203_1004403_+	phospholipase D	NA	NA	NA	NA
WP_110134266.1\|1004681_1006352_-\|tRNA	arginine--tRNA ligase	NA	NA	NA	NA
WP_035190070.1\|1006348_1006789_-	DUF1934 domain-containing protein	NA	NA	NA	NA
WP_017550332.1\|1006944_1007817_-	agmatinase	NA	NA	NA	NA
WP_035183221.1\|1007996_1010048_+	penicillin-binding protein	NA	NA	NA	NA
WP_035183194.1\|1010154_1010667_-	hypothetical protein	NA	NA	NA	NA
WP_017550335.1\|1010697_1011360_-\|protease	site-2 protease family protein	NA	NA	NA	NA
WP_071646869.1\|1011475_1011691_+	4-oxalocrotonate tautomerase	NA	NA	NA	NA
WP_017550336.1\|1011705_1012224_-	hypothetical protein	NA	NA	NA	NA
WP_017550337.1\|1012241_1013558_-	HD domain-containing protein	E3T4P8	Cafeteria_roenbergensis_virus	6.6e-26	27.7
WP_017550339.1\|1014050_1014761_+	RsfA family transcriptional regulator	A0A1D6X8E5	Bacillus_phage	4.1e-06	50.0
WP_035183189.1\|1016150_1016984_-	lipoate--protein ligase family protein	NA	NA	NA	NA
WP_014096714.1\|1017763_1018735_-	phosphate acetyltransferase	NA	NA	NA	NA
WP_014096713.1\|1018904_1019660_+	heme-dependent peroxidase	NA	NA	NA	NA
WP_029143103.1\|1019820_1020270_+\|coat	spore coat protein GerQ	NA	NA	NA	NA
WP_110134267.1\|1020309_1020681_-	DUF423 domain-containing protein	NA	NA	NA	NA
WP_014096710.1\|1020852_1021110_-	YwdI family protein	NA	NA	NA	NA
WP_026684560.1\|1021559_1022246_-	uracil-DNA glycosylase	A0A0B5IW78	Pandoravirus	3.4e-50	45.1
WP_026684561.1\|1022395_1022743_+	general stress protein	NA	NA	NA	NA
WP_017550349.1\|1022867_1023140_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_017550351.1\|1023619_1023847_+\|bacteriocin	circular bacteriocin, circularin A/uberolysin family	NA	NA	NA	NA
WP_046722045.1\|1026070_1027591_+\|transposase	IS5-like element ISBco3 family transposase	NA	NA	NA	NA

DBSCAN-SWA_4

1123785 : 1131848

Staphylococcus_phage(66.67%)

protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_014096622.1\|1123785_1124280_-	single-stranded DNA-binding protein	A8ATZ7	Listeria_phage	2.8e-54	67.7
WP_014096621.1\|1124341_1124629_-	30S ribosomal protein S6	NA	NA	NA	NA
WP_014096620.1\|1124882_1125353_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	2.2e-40	55.9
WP_014096619.1\|1125365_1126559_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	7.1e-112	54.1
WP_014096618.1\|1126576_1127224_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	8.8e-40	44.8
WP_142010213.1\|1127204_1128326_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	2.9e-54	37.0
WP_014096616.1\|1128647_1129748_-	redox-regulated ATPase YchF	NA	NA	NA	NA
WP_013860891.1\|1129908_1130109_-	DUF951 domain-containing protein	NA	NA	NA	NA
WP_014096615.1\|1130098_1131010_-	mechanosensitive ion channel family protein	NA	NA	NA	NA
WP_017550665.1\|1131224_1131848_+\|protease	spore protease YyaC	G3M9W0	Bacillus_virus	3.6e-22	38.5

DBSCAN-SWA_5

1349622 : 1391369

uncultured_Caudovirales_phage(50.0%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_043052509.1\|1349622_1350933_+\|transposase	transposase	NA	NA	NA	NA
WP_014096450.1\|1351472_1352684_-	MFS transporter	NA	NA	NA	NA
WP_110133726.1\|1352776_1353352_-	glycine-rich domain-containing protein-like	A0A2I2L429	Orpheovirus	1.8e-07	33.3
WP_035182786.1\|1353992_1355135_-	MFS transporter	NA	NA	NA	NA
WP_110133727.1\|1355332_1356181_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_104851084.1\|1356315_1358001_-\|transposase	IS1634 family transposase	NA	NA	NA	NA
WP_110133728.1\|1358595_1359327_-	NAD-dependent protein deacylase	A0A068EPD4	Bacillus_phage	4.2e-46	41.0
WP_014096446.1\|1359678_1361412_+	chemotaxis protein	A0A2H4J162	uncultured_Caudovirales_phage	3.0e-10	44.3
WP_014096445.1\|1361490_1362348_-	DUF4097 family beta strand repeat protein	NA	NA	NA	NA
WP_014096444.1\|1362340_1362901_-	DUF1700 domain-containing protein	NA	NA	NA	NA
WP_014096443.1\|1362893_1363217_-	PadR family transcriptional regulator	NA	NA	NA	NA
WP_110133729.1\|1363557_1365312_+	methyl-accepting chemotaxis protein	A0A2H4J162	uncultured_Caudovirales_phage	1.4e-10	49.4
WP_014096441.1\|1365485_1366892_-	MFS transporter	NA	NA	NA	NA
WP_014096440.1\|1366958_1367528_-	cysteine hydrolase	NA	NA	NA	NA
WP_014096439.1\|1367639_1368242_+	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_026104499.1\|1368390_1368849_-	hypothetical protein	NA	NA	NA	NA
WP_026104498.1\|1368854_1369643_-	hypothetical protein	NA	NA	NA	NA
WP_014096438.1\|1369949_1370237_+	hypothetical protein	NA	NA	NA	NA
WP_014096437.1\|1370229_1371396_+	MFS transporter	NA	NA	NA	NA
WP_014096436.1\|1371422_1372325_+	ATP-grasp domain-containing protein	NA	NA	NA	NA
WP_046721642.1\|1372386_1372611_+	hypothetical protein	NA	NA	NA	NA
WP_014096435.1\|1372626_1373715_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_026104497.1\|1373895_1374195_+	YkvR family protein	NA	NA	NA	NA
WP_061577476.1\|1374191_1375187_+	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_014096432.1\|1376441_1377671_-	MFS transporter	NA	NA	NA	NA
WP_017550282.1\|1378026_1378566_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_014096428.1\|1378881_1379370_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_013858128.1\|1380090_1381401_+\|transposase	transposase	NA	NA	NA	NA
WP_013858307.1\|1382495_1384181_-\|transposase	IS1634 family transposase	NA	NA	NA	NA
WP_017550280.1\|1384515_1385136_+	hypothetical protein	NA	NA	NA	NA
WP_014096424.1\|1385348_1386617_+	MFS transporter	NA	NA	NA	NA
WP_014096423.1\|1386814_1387255_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_110133730.1\|1387467_1388259_+	DUF2837 family protein	NA	NA	NA	NA
WP_110133731.1\|1388454_1389195_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_110133732.1\|1390031_1391369_-\|transposase	IS1380 family transposase	NA	NA	NA	NA

DBSCAN-SWA_6

1396267 : 1470206

Streptococcus_phage(40.0%)

transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_041847046.1\|1396267_1397839_+\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	8.7e-49	30.6
WP_017550355.1\|1398516_1399830_-\|transposase	IS1380-like element ISBco1 family transposase	A0A1X9I6F6	Streptococcus_phage	7.1e-113	48.8
WP_110133733.1\|1400041_1401781_+	AAA family ATPase	NA	NA	NA	NA
WP_110133734.1\|1401773_1403582_+	ATP-dependent helicase	NA	NA	NA	NA
WP_110133735.1\|1403887_1404457_+	DNA recombinase	A0A2K5B2B4	Erysipelothrix_phage	1.6e-16	30.6
WP_014096263.1\|1404726_1406037_+\|transposase	DDE transposase family protein	NA	NA	NA	NA
WP_012102963.1\|1406613_1407840_+	macrolide efflux MFS transporter Mef(A)	A0A1B0RXG2	Streptococcus_phage	1.9e-208	95.3
WP_110133736.1\|1407953_1409417_+	Msr family ABC-F type ribosomal protection protein	A0A1B0RXA0	Streptococcus_phage	2.1e-238	89.7
WP_110133737.1\|1409973_1411083_+	FMN-binding glutamate synthase family protein	NA	NA	NA	NA
WP_026314590.1\|1411161_1412325_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_110133738.1\|1412448_1413213_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_018664281.1\|1413387_1414809_+	multidrug efflux MFS transporter	NA	NA	NA	NA
WP_018664279.1\|1414939_1415434_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_110133739.1\|1416034_1416676_+	Vat family streptogramin A O-acetyltransferase	A0A1V0SJ47	Klosneuvirus	3.9e-24	35.7
WP_039236463.1\|1416780_1417659_+	AraC family transcriptional regulator	D0R0F8	Streptococcus_phage	7.8e-31	30.9
WP_041901972.1\|1419185_1419497_-	hypothetical protein	NA	NA	NA	NA
WP_110133740.1\|1420085_1420691_+	hypothetical protein	NA	NA	NA	NA
WP_110133741.1\|1422683_1423178_+	hypothetical protein	NA	NA	NA	NA
WP_108897630.1\|1424654_1425248_+	hypothetical protein	NA	NA	NA	NA
WP_108897631.1\|1425353_1425896_+	hypothetical protein	NA	NA	NA	NA
WP_108899067.1\|1426097_1426742_+	signal peptidase I	NA	NA	NA	NA
WP_110133742.1\|1426807_1427485_+	hypothetical protein	NA	NA	NA	NA
WP_034768474.1\|1427584_1428118_+	dihydrofolate reductase	NA	NA	NA	NA
WP_110133743.1\|1428887_1430282_+\|transposase	transposase	NA	NA	NA	NA
WP_110133744.1\|1430421_1431147_-	type II toxin-antitoxin system Phd/YefM family antitoxin	NA	NA	NA	NA
WP_080564932.1\|1431665_1431851_-	hypothetical protein	NA	NA	NA	NA
WP_110133745.1\|1432002_1433412_+	group II intron reverse transcriptase/maturase	A0A0U4J920	Pseudomonas_phage	1.3e-35	30.2
WP_017552043.1\|1433479_1434664_-	hydroxymethylglutaryl-CoA synthase	NA	NA	NA	NA
WP_048339812.1\|1434807_1436223_+\|transposase	ISLre2 family transposase	NA	NA	NA	NA
WP_014096414.1\|1436670_1437849_+	acetyl-CoA C-acetyltransferase	NA	NA	NA	NA
WP_014096413.1\|1438085_1438424_-	transcriptional regulator	NA	NA	NA	NA
WP_014096412.1\|1438553_1439012_-	hypothetical protein	NA	NA	NA	NA
WP_014096411.1\|1439174_1440152_+	D-glycerate dehydrogenase	M1NSB9	Streptococcus_phage	7.6e-19	28.2
WP_017550607.1\|1441479_1442433_+	ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	2.4e-25	33.6
WP_017550606.1\|1442425_1443955_+	ABC transporter permease/substrate-binding protein	NA	NA	NA	NA
WP_014096407.1\|1444487_1444970_+	PTS glucose transporter subunit IIA	NA	NA	NA	NA
WP_104851095.1\|1445000_1446419_+	PTS system trehalose-specific EIIBC component	NA	NA	NA	NA
WP_014096405.1\|1446547_1448224_+	alpha,alpha-phosphotrehalase	NA	NA	NA	NA
WP_014096404.1\|1448264_1448984_+	trehalose operon repressor	NA	NA	NA	NA
WP_014096403.1\|1449077_1450406_-	2-keto-3-deoxygluconate permease	NA	NA	NA	NA
WP_014096401.1\|1450807_1452364_-	gluconokinase	NA	NA	NA	NA
WP_017550602.1\|1452514_1453207_-	GntR family transcriptional regulator	NA	NA	NA	NA
WP_017550601.1\|1453267_1454176_-	decarboxylating 6-phosphogluconate dehydrogenase	A0A1D7RAP9	Synechococcus_phage	6.7e-54	36.0
WP_014096398.1\|1454942_1455404_+	flavodoxin	NA	NA	NA	NA
WP_052042116.1\|1455400_1456486_+	excinuclease ABC subunit C	NA	NA	NA	NA
WP_110133746.1\|1456729_1457482_+	Crp/Fnr family transcriptional regulator	NA	NA	NA	NA
WP_110133747.1\|1457688_1459632_+	cation-translocating P-type ATPase	E4ZFI9	Streptococcus_phage	1.4e-109	38.8
WP_026683770.1\|1459653_1459875_+	heavy-metal-associated domain-containing protein	NA	NA	NA	NA
WP_014096391.1\|1461208_1463443_+	ribonucleoside-diphosphate reductase subunit alpha	A0A0Y0AS84	Bacillus_phage	1.0e-260	61.0
WP_014096390.1\|1463427_1463910_+	flavodoxin	A0A060AL80	Listeria_phage	6.2e-14	36.9
WP_014096389.1\|1463854_1464898_+	ribonucleotide-diphosphate reductase subunit beta	A0A059T7I4	Listeria_phage	7.6e-110	56.6
WP_014096388.1\|1465220_1465835_-	glycerol-3-phosphate acyltransferase	NA	NA	NA	NA
WP_110133748.1\|1465831_1466917_-	glycosyltransferase	NA	NA	NA	NA
WP_048339797.1\|1467185_1468115_+\|transposase	transposase	NA	NA	NA	NA
WP_014096385.1\|1468116_1468353_+	hypothetical protein	NA	NA	NA	NA
WP_014096384.1\|1468349_1468613_+	hypothetical protein	NA	NA	NA	NA
WP_110133749.1\|1468790_1470206_+\|transposase	ISLre2 family transposase	NA	NA	NA	NA

DBSCAN-SWA_7

1717373 : 1779567

Streptococcus_phage(14.29%)

transposase,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_110133805.1\|1717373_1718687_-\|transposase	IS1380-like element ISBco1 family transposase	A0A1X9I6F6	Streptococcus_phage	9.3e-113	48.8
WP_014096168.1\|1719202_1720534_+	MBL fold metallo-hydrolase	Q0H255	Geobacillus_phage	6.0e-75	57.7
WP_013858348.1\|1720549_1720762_+	DUF3006 domain-containing protein	NA	NA	NA	NA
WP_014096165.1\|1726368_1728024_+	APC family permease	NA	NA	NA	NA
WP_110133806.1\|1728149_1730366_-	peptidase	NA	NA	NA	NA
WP_014096162.1\|1730843_1731812_+	LCP family protein	NA	NA	NA	NA
WP_014096161.1\|1732153_1732519_+	hypothetical protein	NA	NA	NA	NA
WP_014096159.1\|1732656_1733574_-	aldo/keto reductase	A0A1V0SDE7	Indivirus	2.4e-06	29.3
WP_110134283.1\|1733755_1734667_+\|transposase	transposase	NA	NA	NA	NA
WP_110133807.1\|1734668_1734920_+	hypothetical protein	NA	NA	NA	NA
WP_017550185.1\|1735050_1735374_+	DUF3870 domain-containing protein	NA	NA	NA	NA
WP_061577482.1\|1735642_1736854_-	butyryl-CoA dehydrogenase	NA	NA	NA	NA
WP_046721832.1\|1736858_1738037_-	CoA transferase	NA	NA	NA	NA
WP_046721833.1\|1738762_1739776_+	NADP-dependent oxidoreductase	NA	NA	NA	NA
WP_110133808.1\|1740315_1741515_+	MFS transporter	NA	NA	NA	NA
WP_110133809.1\|1741673_1743536_+	transcription antiterminator	NA	NA	NA	NA
WP_014096149.1\|1743660_1743993_+	PTS sugar transporter subunit IIB	NA	NA	NA	NA
WP_110133810.1\|1744010_1744340_+	PTS lactose/cellobiose transporter subunit IIA	NA	NA	NA	NA
WP_014096147.1\|1744373_1745459_+	DUF871 domain-containing protein	NA	NA	NA	NA
WP_061087168.1\|1745471_1746755_+	PTS cellobiose transporter subunit IIC	NA	NA	NA	NA
WP_110133811.1\|1746817_1748230_-	MFS transporter	NA	NA	NA	NA
WP_110133812.1\|1748706_1750125_-	amino acid permease	NA	NA	NA	NA
WP_142010231.1\|1750504_1751608_+	hypothetical protein	NA	NA	NA	NA
WP_110133813.1\|1751795_1752986_+	glycine C-acetyltransferase	D2TEZ5	Emiliania_huxleyi_virus	3.8e-49	32.6
WP_142010234.1\|1753046_1754033_+	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_110133815.1\|1754410_1754839_+	MarR family transcriptional regulator	NA	NA	NA	NA
WP_110133816.1\|1754835_1756035_+	MFS transporter	NA	NA	NA	NA
WP_017551896.1\|1756373_1757360_+	LacI family DNA-binding transcriptional regulator	NA	NA	NA	NA
WP_110133817.1\|1757554_1759552_+	beta-galactosidase	NA	NA	NA	NA
WP_110133819.1\|1759817_1760495_-	ABC transporter permease	NA	NA	NA	NA
WP_014096132.1\|1760506_1761415_-	osmoprotectant ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_014096131.1\|1761430_1762084_-	ABC transporter permease	NA	NA	NA	NA
WP_014096130.1\|1762095_1763241_-\|holin	betaine/proline/choline family ABC transporter ATP-binding protein	F2Y1V5	Organic_Lake_phycodnavirus	1.5e-13	28.8
WP_014096129.1\|1763425_1763971_+	GbsR/MarR family transcriptional regulator	NA	NA	NA	NA
WP_017551900.1\|1763985_1764546_+	maltose O-acetyltransferase	NA	NA	NA	NA
WP_110134284.1\|1764819_1765857_-	SDR family oxidoreductase	A0A0M4JSW6	Mollivirus	5.8e-09	24.1
WP_110133743.1\|1766003_1767398_-\|transposase	transposase	NA	NA	NA	NA
WP_061577833.1\|1767569_1768598_+\|transposase	IS1595 family transposase	NA	NA	NA	NA
WP_061577834.1\|1768654_1769224_+	dihydrofolate reductase	NA	NA	NA	NA
WP_013858390.1\|1769724_1770018_-	hypothetical protein	NA	NA	NA	NA
WP_110133820.1\|1770168_1770741_-	cupin domain-containing protein	NA	NA	NA	NA
WP_035191172.1\|1771044_1771860_+	SGNH/GDSL hydrolase family protein	NA	NA	NA	NA
WP_035182475.1\|1772483_1773200_+	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_110133821.1\|1773640_1775050_+	group II intron reverse transcriptase/maturase	A0A0U4J920	Pseudomonas_phage	1.5e-36	30.5
WP_014096121.1\|1777070_1778648_+	YifB family Mg chelatase-like AAA ATPase	NA	NA	NA	NA
WP_014096120.1\|1778592_1779567_+\|transposase	transposase	NA	NA	NA	NA

DBSCAN-SWA_8

2130251 : 2136485

Streptococcus_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_110133866.1\|2130251_2131199_+	thioredoxin-disulfide reductase	G3MA85	Bacillus_virus	9.1e-86	53.1
WP_110133867.1\|2131725_2131929_+	hypothetical protein	NA	NA	NA	NA
WP_014095823.1\|2132037_2132496_+	8-oxo-dGTP diphosphatase	K4F7D9	Cronobacter_phage	6.9e-07	33.3
WP_014095822.1\|2132532_2133423_+	RNase adapter RapZ	A0A0R8VB27	Thermobifida_phage	4.3e-05	29.8
WP_061086719.1\|2133419_2134400_+	YvcK family protein	A1IMD5	Streptococcus_phage	1.2e-67	44.6
WP_013858691.1\|2134480_2135434_+	DNA-binding protein WhiA	Q7AWZ3	Streptococcus_phage	9.2e-54	39.1
WP_014095819.1\|2135544_2135814_+	HPr family phosphocarrier protein	NA	NA	NA	NA
WP_035182139.1\|2135900_2136485_-	ATP-dependent Clp endopeptidase proteolytic subunit ClpP	A0A223W000	Agrobacterium_phage	1.3e-53	56.0

DBSCAN-SWA_9

3294022 : 3353851

Moraxella_phage(28.57%)

coat,tRNA,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_014097876.1\|3294022_3295294_-\|coat	SafA/ExsA family spore coat assembly protein	S6BFI4	Thermus_phage	6.2e-05	55.6
WP_026683597.1\|3295480_3296038_+	transcription repressor NadR	NA	NA	NA	NA
WP_014097874.1\|3296165_3297011_-	prephenate dehydratase	NA	NA	NA	NA
WP_014097873.1\|3297036_3297489_-	ACT domain-containing protein	NA	NA	NA	NA
WP_017551053.1\|3297537_3298830_-	GTPase ObgE	NA	NA	NA	NA
WP_026683598.1\|3298864_3299401_-	sporulation protein	NA	NA	NA	NA
WP_013859801.1\|3299606_3299897_-	50S ribosomal protein L27	NA	NA	NA	NA
WP_014097870.1\|3299909_3300239_-\|protease	ribosomal-processing cysteine protease Prp	NA	NA	NA	NA
WP_013859803.1\|3300251_3300560_-	50S ribosomal protein L21	NA	NA	NA	NA
WP_035184501.1\|3300702_3302181_-	Rne/Rng family ribonuclease	NA	NA	NA	NA
WP_014097868.1\|3302232_3303099_-	stage IV sporulation protein FB	NA	NA	NA	NA
WP_017551058.1\|3303091_3303844_-	M23 family metallopeptidase	NA	NA	NA	NA
WP_110134027.1\|3303970_3304780_-	septum site-determining protein MinD	NA	NA	NA	NA
WP_035184496.1\|3304772_3305465_-	septum site-determining protein MinC	NA	NA	NA	NA
WP_017551061.1\|3305689_3306208_-	rod shape-determining protein MreD	NA	NA	NA	NA
WP_017551062.1\|3306207_3307074_-	rod shape-determining protein MreC	NA	NA	NA	NA
WP_017551063.1\|3307180_3308197_-	rod shape-determining protein	NA	NA	NA	NA
WP_017551064.1\|3308370_3309054_-	JAB domain-containing protein	NA	NA	NA	NA
WP_014097863.1\|3309253_3310237_-	hypothetical protein	NA	NA	NA	NA
WP_014097862.1\|3310355_3311117_-	prepilin peptidase	NA	NA	NA	NA
WP_014097861.1\|3311224_3311929_-	type 4a pilus biogenesis protein PilO	NA	NA	NA	NA
WP_014097860.1\|3311925_3312774_-	PilN domain-containing protein	NA	NA	NA	NA
WP_026683603.1\|3312774_3313773_-	pilus assembly protein PilM	NA	NA	NA	NA
WP_014097858.1\|3313865_3314288_-	prepilin-type N-terminal cleavage/methylation domain-containing protein	NA	NA	NA	NA
WP_014097857.1\|3314370_3315576_-	type II secretion system F family protein	NA	NA	NA	NA
WP_014097856.1\|3315562_3316615_-	type IV pilus twitching motility protein PilT	NA	NA	NA	NA
WP_014097855.1\|3316624_3318286_-	Flp pilus assembly complex ATPase component	NA	NA	NA	NA
WP_035184493.1\|3318331_3319786_-	hypothetical protein	NA	NA	NA	NA
WP_014097853.1\|3319802_3320531_-	photosystem reaction center subunit H	NA	NA	NA	NA
WP_110134028.1\|3320557_3322303_-	hypothetical protein	NA	NA	NA	NA
WP_110134029.1\|3322430_3324092_-	hypothetical protein	NA	NA	NA	NA
WP_035188277.1\|3324091_3324601_-	pilin	NA	NA	NA	NA
WP_035188280.1\|3324597_3325017_-	prepilin-type N-terminal cleavage/methylation domain-containing protein	NA	NA	NA	NA
WP_110134030.1\|3325135_3326458_-	bifunctional folylpolyglutamate synthase/dihydrofolate synthase	NA	NA	NA	NA
WP_026683610.1\|3326520_3329166_-\|tRNA	valine--tRNA ligase	A0A1V0S951	Catovirus	8.8e-163	43.9
WP_014097848.1\|3329592_3329784_+	hypothetical protein	NA	NA	NA	NA
WP_014097847.1\|3329800_3330985_-\|coat	spore coat protein YsxE	NA	NA	NA	NA
WP_110134031.1\|3331015_3332833_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_014097845.1\|3333218_3334508_-	glutamate-1-semialdehyde 2,1-aminomutase	A0A1V0SKB7	Klosneuvirus	4.4e-06	27.6
WP_014097844.1\|3334523_3335501_-	porphobilinogen synthase	NA	NA	NA	NA
WP_110134032.1\|3335737_3336526_-	uroporphyrinogen-III synthase	NA	NA	NA	NA
WP_014097842.1\|3336522_3337455_-	hydroxymethylbilane synthase	NA	NA	NA	NA
WP_014097841.1\|3337467_3338292_-	cytochrome c biogenesis protein CcsA	NA	NA	NA	NA
WP_014097840.1\|3338307_3339639_-\|tRNA	glutamyl-tRNA reductase	NA	NA	NA	NA
WP_014097839.1\|3339824_3340319_+	hypothetical protein	NA	NA	NA	NA
WP_014097838.1\|3340495_3341080_-	YihA family ribosome biogenesis GTP-binding protein	NA	NA	NA	NA
WP_061565532.1\|3341076_3343401_-	endopeptidase La	A0A0R6PGP8	Moraxella_phage	4.8e-181	44.5
WP_061565531.1\|3343444_3345082_-\|protease	ATP-dependent protease LonB	A0A0R6PGP8	Moraxella_phage	5.0e-15	36.4
WP_014097835.1\|3345373_3346642_-\|protease	ATP-dependent protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	5.4e-150	67.4
WP_061565530.1\|3347010_3348297_-	trigger factor	NA	NA	NA	NA
WP_014097833.1\|3348460_3349453_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_014097832.1\|3349592_3350036_-	YndM family protein	NA	NA	NA	NA
WP_061086562.1\|3350170_3350467_+	hypothetical protein	NA	NA	NA	NA
WP_014097829.1\|3350945_3351455_-	metallophosphoesterase	NA	NA	NA	NA
WP_014097828.1\|3351451_3352060_-	XTP/dITP diphosphatase	A0A2H4UUV7	Bodo_saltans_virus	8.1e-11	33.3
WP_014097827.1\|3352167_3353208_-	sporulation protein	NA	NA	NA	NA
WP_110134033.1\|3353351_3353552_+	hypothetical protein	NA	NA	NA	NA
WP_071451963.1\|3353548_3353851_+\|coat	spore coat protein	NA	NA	NA	NA

DBSCAN-SWA_10

3569449 : 3606793

Bacillus_phage(37.5%)

transposase,bacteriocin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_046721937.1\|3569449_3570100_-\|bacteriocin	putative bacteriocin export ABC transporter	G9BWD6	Planktothrix_phage	1.6e-20	30.7
WP_110134052.1\|3570101_3571082_-	DUF1430 domain-containing protein	NA	NA	NA	NA
WP_104851084.1\|3571223_3572909_-\|transposase	IS1634 family transposase	NA	NA	NA	NA
WP_110134053.1\|3572952_3574248_-	hypothetical protein	NA	NA	NA	NA
WP_035191149.1\|3574545_3574725_-	hypothetical protein	NA	NA	NA	NA
WP_061577719.1\|3575025_3575931_-	DMT family transporter	NA	NA	NA	NA
WP_013860047.1\|3576021_3576711_+	MgtC/SapB family protein	G3MA03	Bacillus_virus	3.0e-14	35.7
WP_081106251.1\|3576846_3577971_-	DUF1646 family protein	NA	NA	NA	NA
WP_061565795.1\|3578480_3578867_-	MFS transporter	NA	NA	NA	NA
WP_142010266.1\|3579174_3580860_+\|transposase	IS1634 family transposase	NA	NA	NA	NA
WP_104851503.1\|3581126_3583538_-	copper-translocating P-type ATPase	A0A218MNH6	uncultured_virus	4.8e-115	38.0
WP_104851504.1\|3583631_3583838_-	copper chaperone CopZ	NA	NA	NA	NA
WP_013860052.1\|3583852_3584197_-	metal-sensing transcriptional repressor	NA	NA	NA	NA
WP_104851505.1\|3584476_3585892_+\|transposase	ISLre2 family transposase	NA	NA	NA	NA
WP_110134054.1\|3586224_3587529_+\|transposase	IS1380-like element ISBco2 family transposase	NA	NA	NA	NA
WP_081110520.1\|3587684_3587957_+	metal-sensing transcriptional repressor	NA	NA	NA	NA
WP_061566880.1\|3588057_3588468_-	Lrp/AsnC family transcriptional regulator	NA	NA	NA	NA
WP_104851507.1\|3588574_3588994_+	carboxymuconolactone decarboxylase family protein	NA	NA	NA	NA
WP_104851508.1\|3589021_3589204_+	hypothetical protein	NA	NA	NA	NA
WP_104851509.1\|3589274_3590462_+	amidohydrolase	NA	NA	NA	NA
WP_013860056.1\|3590522_3590717_+	DUF3311 domain-containing protein	NA	NA	NA	NA
WP_046721674.1\|3590713_3592183_+	sodium:solute symporter	NA	NA	NA	NA
WP_013860060.1\|3592854_3593073_-	DUF2933 domain-containing protein	NA	NA	NA	NA
WP_013860062.1\|3593289_3593727_+	hypothetical protein	NA	NA	NA	NA
WP_046721673.1\|3593757_3595155_+	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	9.8e-36	34.8
WP_017554156.1\|3595129_3595804_+	response regulator transcription factor	W8CYM9	Bacillus_phage	3.8e-38	35.6
WP_013860065.1\|3595875_3596430_-	YdhK family protein	NA	NA	NA	NA
WP_080952267.1\|3596610_3597222_+	SDR family oxidoreductase	NA	NA	NA	NA
WP_046721671.1\|3597235_3597889_-	lipoprotein	NA	NA	NA	NA
WP_026685174.1\|3597885_3598821_-	polysaccharide deacetylase	A0A1V0SLN0	Klosneuvirus	3.7e-07	25.7
WP_110134055.1\|3600601_3601933_-	chloride channel protein	NA	NA	NA	NA
WP_014097608.1\|3602399_3602696_-	rhodanese-like domain-containing protein	A0A2H4PQR9	Staphylococcus_phage	4.2e-13	39.6
WP_014097607.1\|3602777_3603038_-	metal-sensitive transcriptional regulator	NA	NA	NA	NA
WP_035184240.1\|3603619_3604408_+	endonuclease	A0A1P8CWK6	Bacillus_phage	1.4e-60	65.2
WP_017551018.1\|3604510_3605020_-	PTS glucose transporter subunit IIA	NA	NA	NA	NA
WP_142010269.1\|3605377_3606793_-\|transposase	ISLre2 family transposase	NA	NA	NA	NA

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP033687

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection