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_CP013673	Bifidobacterium longum strain 35624, complete genome	6 crisprs	WYL,DEDDh,cas2,cas1,cas4,cas7,cas8c,cas5,cas3,casR	1	44	3	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP013673_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_1

171510-171878

Orphan

Consensus_repeat	Method
CGATGACCCGTGGAATCAACCGCA	CRISPRCasFinder

6 spacers

The CRISPR arrays of NZ_CP013673_1

>merge|NZ_CP013673|1|171510-171878|CRISPRCasFinder
CGACGATCCATGGAATCAGACGCAGTCTCAGGCCGCGGTCTCACCGGCGTCGCAACCGGCCGAAGCCGACCCGTGGAACCAGCCATATCAGCAGTCTCCTCACGATGATCCGTGGAATCAACCGCAGGGGAACCATGCTCAGGCGGCTCCGCAGCCAGGAGACGACCCGTGGAATCAGCCTCAGTCCCAGACTCCGGCTTCTTCGGTTCCTCAGACAGTGTCGGGCAATATGTCGGGCGATGACCCGTGGAACCAGCCCCAATCGGTTCCGCAGCCGGCTGCCGGCGATGACCCGTGGAATCAACCGCAGGCAGTTCCACAATCGGCTCCGCAGGCCACCCCGCACGGTGACCCGTGGAATCAACCGCA

>NZ_CP013673|1|1|171510-171878|CRISPRCasFinder
CGACGATCCATGGAATCAGACGCA	GTCTCAGGCCGCGGTCTCACCGGCGTCGCAACCGGCCGA
AGCCGACCCGTGGAACCAGCCATA	TCAGCAGTCTCCTCA
CGATGATCCGTGGAATCAACCGCA	GGGGAACCATGCTCAGGCGGCTCCGCAGCCAGG
AGACGACCCGTGGAATCAGCCTCA	GTCCCAGACTCCGGCTTCTTCGGTTCCTCAGACAGTGTCGGGCAATATGTCGGG
CGATGACCCGTGGAACCAGCCCCA	ATCGGTTCCGCAGCCGGCTGCCGG
CGATGACCCGTGGAATCAACCGCA	GGCAGTTCCACAATCGGCTCCGCAGGCCACCCCGCA
CGGTGACCCGTGGAATCAACCGCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_058101899.1\|167092_168223_+\|diacylglycerol-kinase	unknown	unknown	gnl\|CDD\|237021
NZ_CP013673.1\|WP_007051621.1\|172153_172756_+\|recombination-protein-RecR	unknown	unknown	gnl\|CDD\|234616
NZ_CP013673.1\|WP_011068517.1\|174120_174393_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007051615.1\|177237_177804_+\|ACT-domain-containing-protein	unknown	unknown	gnl\|CDD\|235843
NZ_CP013673.1\|WP_007051614.1\|177885_178980_-\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|236329
NZ_CP013673.1\|WP_011068512.1\|181473_181983_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007051625.1\|166657_167044_+\|flp-pilus-assembly-TadE/G-like-family-protein	unknown	unknown	gnl\|CDD\|274799
NZ_CP013673.1\|WP_007051630.1\|162382_163333_+\|P-loop-NTPase	unknown	unknown	gnl\|CDD\|274798
NZ_CP013673.1\|WP_007051623.1\|168420_169020_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP013673.1\|WP_080749440.1\|179054_179768_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_032742156.1\|165059_165662_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_077387087.1\|166230_166617_+\|pilus-assembly-protein	unknown	unknown	gnl\|CDD\|377921
NZ_CP013673.1\|WP_011068521.1\|165838_166234_+\|DUF4244-domain-containing-protein	unknown	unknown	gnl\|CDD\|379429
NZ_CP013673.1\|WP_007054687.1\|174773_176057_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|379306
NZ_CP013673.1\|WP_011068513.1\|179770_181342_-\|metallophosphatase	unknown	unknown	gnl\|CDD\|277329
NZ_CP013673.1\|WP_015713234.1\|164370_165063_+\|pilus-assembly-protein	unknown	unknown	gnl\|CDD\|227300
NZ_CP013673.1\|WP_007051629.1\|163339_164407_+\|pilus-biosynthesis-protein	unknown	unknown	gnl\|CDD\|200328
NZ_CP013673.1\|WP_007051616.1\|176417_177182_+\|aspartate-kinase	unknown	unknown	gnl\|CDD\|235843
NZ_CP013673.1\|WP_007051631.1\|161434_162160_+\|DedA-family-protein	unknown	unknown	gnl\|CDD\|182775
NZ_CP013673.1\|WP_007054686.1\|172752_173886_-\|class-C-sortase	unknown	unknown	gnl\|CDD\|320676

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_058101899.1\|167092_168223_+\|diacylglycerol-kinase	gnl\|CDD\|237021	PRK11914, PRK11914, diacylglycerol kinase; Reviewed.	2.01063e-31
NZ_CP013673.1\|WP_007051621.1\|172153_172756_+\|recombination-protein-RecR	gnl\|CDD\|234616	PRK00076, recR, recombination protein RecR; Reviewed.	4.73611e-118
NZ_CP013673.1\|WP_007051614.1\|177885_178980_-\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|236329	PRK08664, PRK08664, aspartate-semialdehyde dehydrogenase; Reviewed.	0
NZ_CP013673.1\|WP_007051615.1\|177237_177804_+\|ACT-domain-containing-protein	gnl\|CDD\|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	1.06061e-66
NZ_CP013673.1\|WP_007051625.1\|166657_167044_+\|flp-pilus-assembly-TadE/G-like-family-protein	gnl\|CDD\|274799	TIGR03816, tadE_like_DECH, helicase/secretion neighborhood TadE-like protein. Members of this small, highly hydrophobic protein family occur in a pilus/secretion-like region that usually is next to an uncharacterized DEAH-box helicase, in Actinobacteria. Members show sequence similarity to the TadE-like family described by pfam07811. The function is unknown. [Unknown function, General].	3.91757e-24
NZ_CP013673.1\|WP_007051623.1\|168420_169020_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.0756e-15
NZ_CP013673.1\|WP_007051630.1\|162382_163333_+\|P-loop-NTPase	gnl\|CDD\|274798	TIGR03815, CpaE_hom_Actino, helicase/secretion neighborhood CpaE-like protein. Members of this protein family belong to the MinD/ParA family of P-loop NTPases, and in particular show homology to the CpaE family of pilus assembly proteins (see ). Nearly all members are found, not only in a gene context consistent with pilus biogenesis or a pilus-like secretion apparatus, but also near a DEAD/DEAH-box helicase, suggesting an involvement in DNA transfer activity. The model describes a clade restricted to the Actinobacteria.	9.19902e-11
NZ_CP013673.1\|WP_077387087.1\|166230_166617_+\|pilus-assembly-protein	gnl\|CDD\|377921	pfam07811, TadE, TadE-like protein. The members of this family are similar to a region of the protein product of the bacterial tadE locus. In various bacterial species, the tad locus is closely linked to flp-like genes, which encode proteins required for the production of pili involved in adherence to surfaces. It is thought that the tad loci encode proteins that act to assemble or export an Flp pilus in various bacteria. All tad loci but TadA have putative transmembrane regions, and in fact the region in question is this family has a high proportion of hydrophobic amino acid residues.	1.14561e-06
NZ_CP013673.1\|WP_011068521.1\|165838_166234_+\|DUF4244-domain-containing-protein	gnl\|CDD\|379429	pfam14029, DUF4244, Protein of unknown function (DUF4244). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 66 and 95 amino acids in length. There is a conserved EYA sequence motif.	1.92287e-16
NZ_CP013673.1\|WP_007054687.1\|174773_176057_+\|ATP-binding-protein	gnl\|CDD\|379306	pfam13635, DUF4143, Domain of unknown function (DUF4143). This domain is almost always found C-terminal to an ATPase core family.	1.02552e-37
NZ_CP013673.1\|WP_011068513.1\|179770_181342_-\|metallophosphatase	gnl\|CDD\|277329	cd07383, MPP_Dcr2, Saccharomyces cerevisiae DCR2 phosphatase and related proteins, metallophosphatase domain. DCR2 phosphatase (Dosage-dependent Cell Cycle Regulator 2) functions together with DCR1 (Gid8) in a common pathway to accelerate initiation of DNA replication in Saccharomyces cerevisiae. Genetic analysis suggests that DCR1 functions upstream of DCR2. DCR2 interacts with and dephosphorylates Sic1, an inhibitor of mitotic cyclin/cyclin-dependent kinase complexes, which may serve to trigger the initiation of cell division. DCR2 belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	8.6826e-33
NZ_CP013673.1\|WP_015713234.1\|164370_165063_+\|pilus-assembly-protein	gnl\|CDD\|227300	COG4965, TadB, Flp pilus assembly protein TadB [Intracellular trafficking and secretion].	0.00108122
NZ_CP013673.1\|WP_007051629.1\|163339_164407_+\|pilus-biosynthesis-protein	gnl\|CDD\|200328	TIGR03819, heli_sec_ATPase, helicase/secretion neighborhood ATPase. Members of this protein family comprise a distinct clade of putative ATPase associated with an integral membrane complex likely to act in pilus formation, secretion, or conjugal transfer. The association of most members with a nearby gene for a DEAH-box helicase suggests a role in conjugal transfer.	3.56402e-90
NZ_CP013673.1\|WP_007051616.1\|176417_177182_+\|aspartate-kinase	gnl\|CDD\|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	3.11844e-146
NZ_CP013673.1\|WP_007051631.1\|161434_162160_+\|DedA-family-protein	gnl\|CDD\|182775	PRK10847, PRK10847, DedA family protein.	1.7339e-45
NZ_CP013673.1\|WP_007054686.1\|172752_173886_-\|class-C-sortase	gnl\|CDD\|320676	cd05827, Sortase_C, Sortase domain found in class C sortases. Class C sortases are membrane-bound cysteine transpeptidases broadly distributed in Gram-positive bacteria (mainly present in Firmicutes and Actinobacteria). They function as pilin polymerases responsible for the assembly of pili, which are multi-subunit hair-like fibres that extend from the cell surface to promote microbial adhesion and biofilm formation. First, one or more class C sortases form the long thin shaft of the pilus through linking together pilin subunits via isopeptide bonds. The base of the pilus is then anchored to the cell wall by a housekeeping sortase or, in some cases, the class C sortase itself. Depending upon the organism both the number and type of sortase enzymes involved varies, and in some cases, accessory factors appear to be needed. In three-component spaA pilus from Corynebacterium diphtheriae, the prototypical class C sortase (named Cd-SrtA) catalyzes polymerization of the SpaA-type pilus, consisting of the shaft pilin SpaA, tip pilin SpaC and minor pilin SpaB. The pilus shaft is then attached to the cell wall by a housekeeping class E sortase, Cd-SrtF. In the absence of Cd-SrtF, Cd-SrtA attaches the pilus to the cell wall, albeit at a reduced rate. Cd-SrtA can recognize two distinct sorting signals (LPLTG in SpaA and SpaC, and LAFTG in SpaB) and it can employ lysine residues that originate from different proteins (either Lys190 within the pilin motif of SpaA or Lys139 in SpaB). However, Cd-SrtA cannot be able to polymerize the major pilin subunit SpaH, even though it contains LPLTG motif. In two-component pili of prototypical Bacillus cereus, the class C sortase (named Bc-SrtD) cleaves related sorting signals within a major pilin protein BcpA (LPVTG) and a minor tip pilin BcpB (IPNTG), and catalyzes a transpeptidation that joins the threonine residues in each signal to the side-chain of Lys162 in BcpA (located within a pilin motif). Unlike the SpaA pilus in C. diphtheriae, in B. cereus Bc-SrtD is unable to covalently attach the pilus to the cell wall without the help of the housekeeping sortase.	1.19515e-84

>NZ_CP013673.1|WP_007051623.1|168420_169020_-|TetR/AcrR-family-transcriptional-regulator
MSDTLDEKRPTRGDARRDAIVQAARKVCLEKGFSKITVSDIASEVGMTRSLFYHYFEDKEAVADAVLDNVIDEILTTLKQWNQARETGNVNKALDDIVHVLRSLIADESPFSNRMIQDGNAELYIKFIDRAADRIADYIAQTTVRDFEQMHGLPITNVHETFFTLIVGLISLIRSHPNISDRTIKEVMAQTLHIESYVV
>NZ_CP013673.1|WP_058101899.1|167092_168223_+|diacylglycerol-kinase
MSESERNERRRVVAMVGNPTSDKGRGAKVDAQVLGLLEEAGRAHNFDVIDITGTSFDDSLNQAREREHEYDYLVVVGGDGMIALGANAVGCSGKPLGIVATGSGNDFARGLKLPVNRIETAVEGIVGAIVRGSHIDVDMGRVTSLDGGYAVDPSTGEEYEYQESKSAEHPIDRYYAGMLSCGLDASINDRANHSHLPTGTMRYFAAVLVELTHMKRYGYHIKATLADGTTDERDIITPLLTIANSRHIGGGIEVSPYSCFSDGLLDLVWMDHVPNFGECAVAISNAYNGKLLASKVFGWKRIREIEVTRAAEGDEPPVLMADGEYIGHLPFRVVAEDCALRVLVPPAVAAREVDSRQEVLDVIARDGRDPVTGQFA
>NZ_CP013673.1|WP_007051625.1|166657_167044_+|flp-pilus-assembly-TadE/G-like-family-protein
MQGMRYEEGSGTMAGAMLVMVVGIALAVAASVGNLMICQNRARSLADLIAFDAAYALWHADIGDPCALAANMAEANGVVLGSCSVRDEDVLVTIKVETMVLVASSVERMARAGPVSCTEGDNYHNNGP
>NZ_CP013673.1|WP_077387087.1|166230_166617_+|pilus-assembly-protein
MTAMKTMTCRWRLARLPPDLCTGSATAEFAIVLPSIIAIAGLILAIGRVVIVSMDCQSAAAAAAREFVVTGDESSARSIAADVAGGKPHVSIAHDGQSTSVTVECSVLPGPLDVTPTRVTGNATAISQ
>NZ_CP013673.1|WP_011068521.1|165838_166234_+|DUF4244-domain-containing-protein
MVCTPRQPGAGANHSHTHGEGAKPLRSFPSLPKGTPMNTPIPVIVDGQAGIFAHSKARVATLNAKAKERLCLMDARIRTLMAEPEEGAATAEYAVVLVAATGFAAVLVAILKSDAIKTLLTNIIKQALKVG
>NZ_CP013673.1|WP_032742156.1|165059_165662_+|hypothetical-protein
MSTVWVHAAAGCAAIASWLYKAPSCHDSRLPGEEPAVAHDCGSSWTILILRMSQVSLRQGSSIPRALDMVGKAVGGDCGARMSEVGSSLARGVPWADAWHAAMAVQHEGAPADSSSGKRTSRTQRDLGLLQSALESSWTHGDMPGVRLESAIEQLDRDERAAIERNAAKLSVKLLMPTGLCFLPAFVLVGVIPAIASFMM
>NZ_CP013673.1|WP_015713234.1|164370_165063_+|pilus-assembly-protein
MGHRSRAEWWWVMMWCAVLVALAVLIWPGNKSGRLYRLAYRGRAVDSAAINEPRYAGSPRVGVAQVITSAIARLRGGGTLVEAFEEQSSRRFATQRITVERLITVFEQRRLPDESPAQVLEAARGVTAAAVLSDELGCQAVPCLEAVLTAYRQMRLMQNLRSQACAVPKATVGLLSALPAVTVALGELLGARPLAFLLGSPRGVVCLVLGGCCYAAGLAWMRALLKGSGL
>NZ_CP013673.1|WP_007051629.1|163339_164407_+|pilus-biosynthesis-protein
MAAVITRADEPGAVPRTVFFGLLNDVASDPQVTDLAVTCDGRVWADRGNGMRETVLRVPFRSPQVVREYAVQLCAQLGRRLDDACPIADAASPDGIRVHAVIAPLVPQGAAISIRFPDRTMASLRHLSQLGVFPAAWLPMFVGLVRRHATVLITGGTGVGKTTLLKALLAQCDVNERIVTVEEVRELGELGRGDHVSLVTREANVEGVGAISLTDLVKATLRMRPDRVVLGECRGAEIVDLLRAFNSGHHGGMTTVHADGVNRVPSRLISLGLLAGVSPQALAMLAAGAFDAVVHLERVNGQRRITQIGELRVAHGELAGTPLAVWNGCHPPRYAAEWGHFIERWGIVPGPSGGG
>NZ_CP013673.1|WP_007051630.1|162382_163333_+|P-loop-NTPase
MNSNTTPRVARRITSPAVAPPGIPLPTDDAPIPAHRYYTPPPRPLASCERQRSGEAPALALTTDTSFHNIVTMTSGHGGVGLSVMASMLAWTLARREHSCALIDADFVAGCLDLLLGVEREPGLRFSQVDAPLGRIEGDAMNHELMMWEGVRVLPYDPWSARQPDWWEVQAAIRALAETNDVVIVDAGQGGLIETVPDLRSGMQVIAAELSVMGLARAKSHRSRLDSWGCEAPHIVGVEPRGAPRGRGHVGIGEAQDYLTATVLGPVKPSVNLCGDVLEGLGIRSVTKGSRKAVSLLADLVEQAIRPVSGASCKDR
>NZ_CP013673.1|WP_007051631.1|161434_162160_+|DedA-family-protein
MGFVNFIIELLKDPRAAIAGWIAMGVAPTLGFIFLIVFIETGVVFFPFLPGDSLLFAAGVFAAPDAATGKAALPLFWLLPVVWCAPIIGDQCNYFIGHFFGRRIIQSGKVKALTPERLAKTEGMIEKWGPLAVFLGRFFPFIRTFMPFISGISGMRWSRFTPFSVLGGLCWSTLFTLLGYFFGNIPAVQDHFELVIVLILLVSLAPTIIGLLKAKFGKKKPAKVTDAQLDVMEDGIKNLDK
>NZ_CP013673.1|WP_007051621.1|172153_172756_+|recombination-protein-RecR
MALAYDGAIQRLIDAFGRLPGIGPKGAQRIAFYMLSAPEDEARDLAEAIEEVKAKIRFCDICGNVCESSPCPVCADPRRDRSVICVVEEPKDVMSIERTREYHGLYHVLGGAINPMANVGPADLRIPGLLKRLEGDEVKEVIMALDPNIEGEATTSYLTQLLRPVGVKVTRLASGLPVGSDLEYADEITLGRALAGRREA
>NZ_CP013673.1|WP_007054686.1|172752_173886_-|class-C-sortase
MALLHRRSTSKRASQKMWENNAAMPDDASANDNVSSARPEPAAFVPTPFDEVIDISDLVAERRRLQRNLWAMRIITIVLLIAAIAVACFPLALQFESDRNLAATTATTAKEVAGWPYPQAEDKLTAARAYNKKLAESGQPILGEAVDPFAAAQGGSQASGEDSASKKDKEYQSLLNTGNGVMGTIKVPKQSINLPFYHGTSEEALASGAGHLYGTSLPVGGKSTHSVITGHRGLVEALMFTRLDEVKEGDFFYIEVMGETLGYKVDRISVILPDDTSKLKIVPGEDRVTLMTCTPYGVNTHRLLISGHRVAIPMPAPEPNDVLDARNIALGVGLGILAAGLFIIWLARRHKAARIIRHGAFWPWMRRKGESANDTLA
>NZ_CP013673.1|WP_011068517.1|174120_174393_-|hypothetical-protein
MIHFFGRKTEYAGTPLTPTKPTARRRTDIHENSNSASFIEVTYSLFMHSYPPYLKALPNIADAATYHVAILCNPLHPLASQRLVRSKPHH
>NZ_CP013673.1|WP_007054687.1|174773_176057_+|ATP-binding-protein
MAVESSEIQRGEYLPRVADGLLTQALQSSGAVQIKGPKWCGKTATAERQSASQVFMQDPDRSATLLALADTKPSLILRGEEPRLIDEWQMAPQLWDAVRFAIDRGRGRGRFILTGSATPQQEPAHSGVGRIARLTMRTMSLFESQESTGVVSLGELFDGNHDVSGFSDFDIENTAFALCRGGWPEAVVESRVNVALRMAADYVEELLDSDINRMDGIKRNKTWMRLIMRSYARNISSQASQSTIAADMQGEPPSEGTLSDYLDALSRACVTEDLPAWNPRLRSKTAVRTSPTRHFSDPSIACAVLHATPEKLLNDFETFGLLFESMCIRDLRVYADALGGDVFHYRDKTGLESDAVIGLHDGRWALIEVKLGEKQVDIAAAHLKKLADRIDQDHEGRPSFLMVLTATAAAYRRDDGVLVVPLATLAP
>NZ_CP013673.1|WP_007051616.1|176417_177182_+|aspartate-kinase
MALIVQKYGGSSVADTESIKRVAKRVVETEKKGNKVAVVVSAMGDTTDDLIDQALSIDSNPPEREMDMLMTAGERISMSLLAMAIHAEGSRAHSFTGQQAGFFTDARYGAAHIKAVRPDRVKNALSLGDIAIVAGFQGINAKGDATTLGRGGSDTSAVALAVALGADICEIYTDVDGIFTADPRIVPSARRIPSIDYESILEMASCGSKVLALRCVEYAQRFNMPLHVRSSFSRRPGTLVVPDGIDPRTLPNLD
>NZ_CP013673.1|WP_007051615.1|177237_177804_+|ACT-domain-containing-protein
MTEEEAKSMGDLFPDLGPEAPVISGIAHDRSEALATVRGVPNEPGMAAKVFTELATAGVNVDMIVQAGASVGTADISFTVPESAVKQVQNTLLDKQEVLGYHSFDVDTNVGKVAVVGVGMKTHAGLAAKFFQALSDEGINVLMISTSEIRIAALVPLDQLNDAVKALHTAYGLDADQIEAVVYGGTGR
>NZ_CP013673.1|WP_007051614.1|177885_178980_-|aspartate-semialdehyde-dehydrogenase
MSEKLKVGILGATGMVGQRFITLLENHPWFEVVTLAASAHSAGKTYAEAVGDRWKMETPMPEYVKNMVVVDGDDAESVASGVDFMFSAVNMPKDQIRAIEERYAKTETPVVSNNSAHRWTPDVPMVVPEINPEHFEVIEHQRKRLGTTRGFIAVKPNCSIQAYTPALAAWKEFEPREVVVSTYQAISGAGKTFKDWPEMVGNIIPFISGEEAKSEKEPLKVFGHVDAAKGEIVPFDGDLKITSQCIRVPVLNGHTATVFLNFGKKATKEELIDRLVNYTSKASELELPHAPKHFIQYLTEDDRPQVKLDVDYEGGMGVSIGRLREDSIFDWKFVGLAHNTLRGAAGGALECAEMLKALGYITKK
>NZ_CP013673.1|WP_080749440.1|179054_179768_+|hypothetical-protein
MQLYETRGTTAVVFPDGGCPMKRRRCSTLVAMSIASVEAQKQLDRIVALGYPDVADISAAAFRSLARPLIGALEHSDLGSNILLVPTRELVSPESLIARTSINRMAGFTTMPPRDIASFLLQDGFMPPEGPFYLVVNPHTGTCYVNREPDVARKLIDSDERLPLTLEEGLAIATQHPEWLLEKNGFNLLGSRSADGRVPSIWMSQNAPRLGAVWPNSRHTWLGNAYCTARRGVSLFK
>NZ_CP013673.1|WP_011068513.1|179770_181342_-|metallophosphatase
MRFREDGSFRVLQMADVQDGPDVLPDTIRLIREAIREADPDLVVFTGDQIRGYDPAYIDTFLRRRGEEPGARVRAVTEIEAKIRGIKRHPVIRKTSDRVADRLTEAGKPVPAALLDPDTVTNAVAAAGADSTDVITTSEVGDSVETSPTPETVSTLVYSTQSGKASPAHETPATLDELMIETREKVRRTFSGFLGPVVEAGVPFAATYGNHDFQCGILADEQDDIYREYPGCLNPDDSLEPGTFALPVESSDGSGRVAMSVMMVNSGDYAGKPEENDAQYPAYVVNPRGLDLADADGYGTPTPKAIEWLGSVQTELGERNGDGKPVPAIAFQHIPPQEFYDCLKEVPAWTPNAVEGARTHAGRCYVLNHEVCRPGSRLGEAIGCADENVGEVDALREAGGYFALFCGHDHKNSFVGHVHDIDLGYAPTCGFECYGPKSRYRGIRLFEFHESNPAGYVTRMLTWGNLVGRYSSNELRVWFEDHCVTGAVSARNELRRPQVFAVVAGAMSLGFIAIIRSLIKAAR
>NZ_CP013673.1|WP_011068512.1|181473_181983_-|hypothetical-protein
MPGRRRATRICQYARNILQAGSGKPAGNAVSWHLLMHLADMRALSVGAGPRFDSGTTPRLRYPTRWPSIRRRRAKYWYCTDSQTAQRRQRTNLWRNTDSGKAYRRQIARLWHTTDATRPTTIGNATNIGPPPTLASLSVGAGPFYESVTTPMVSERQHRDAVWISTDAA

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Crispr_ID: NZ_CP013673_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_2

289528-289613

Orphan

Consensus_repeat	Method
GACAGCTCCCGCCAGCGGGAGCACTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013673_2

>merge|NZ_CP013673|2|289528-289613|CRISPRCasFinder
GACAGCTCCCGCCAGCGGGAGCACTTATTTGTAGGGAAATTCTCCAGTTCAAATCCGTTAGACAGCTCCCGCCAGCGGGAGCCTTT

>NZ_CP013673|2|2|289528-289613|CRISPRCasFinder
GACAGCTCCCGCCAGCGGGAGCACTT	ATTTGTAGGGAAATTCTCCAGTTCAAATCCGTTA
GACAGCTCCCGCCAGCGGGAGCCTTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_007051524.1\|297558_297948_+\|chorismate-mutase	unknown	unknown	gnl\|CDD\|181719
NZ_CP013673.1\|WP_007051537.1\|282924_284328_+\|DNA-recombination-protein-RmuC	unknown	unknown	gnl\|CDD\|376878
NZ_CP013673.1\|WP_007051520.1\|304846_305533_-\|endonuclease-III	unknown	unknown	gnl\|CDD\|223255
NZ_CP013673.1\|WP_007051530.1\|287932_289432_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	unknown	unknown	gnl\|CDD\|235489
NZ_CP013673.1\|WP_003828150.1\|290802_291117_+\|DUF2469-domain-containing-protein	unknown	unknown	gnl\|CDD\|313765
NZ_CP013673.1\|WP_013582355.1\|298069_300154_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_058101885.1\|293362_294976_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235967
NZ_CP013673.1\|WP_007057703.1\|303258_304725_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173859
NZ_CP013673.1\|WP_007051540.1\|278941_279676_+\|aquaporin-family-protein	unknown	unknown	gnl\|CDD\|223653
NZ_CP013673.1\|WP_011068470.1\|291323_293144_+\|histidine-type-phosphatase	unknown	unknown	gnl\|CDD\|132717
NZ_CP013673.1\|WP_007056499.1\|284396_284954_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_058101884.1\|295181_297251_+\|transcription-termination-factor-Rho	unknown	unknown	gnl\|CDD\|237171
NZ_CP013673.1\|WP_007051535.1\|285047_285896_+\|RNA-methyltransferase	unknown	unknown	gnl\|CDD\|349969
NZ_CP013673.1\|WP_007054751.1\|286365_287907_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	unknown	unknown	gnl\|CDD\|234572
NZ_CP013673.1\|WP_007051542.1\|277028_278708_+\|phosphoenolpyruvate--protein-phosphotransferase	unknown	unknown	gnl\|CDD\|224006
NZ_CP013673.1\|WP_011068468.1\|300379_303220_-\|valine--tRNA-ligase	unknown	unknown	gnl\|CDD\|380147
NZ_CP013673.1\|WP_007051539.1\|279759_282468_-\|HAD-IC-family-P-type-ATPase	unknown	unknown	gnl\|CDD\|319774
NZ_CP013673.1\|WP_007051538.1\|282579_282861_+\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224848
NZ_CP013673.1\|WP_011068472.1\|289754_290792_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379112
NZ_CP013673.1\|WP_011068473.1\|286062_286362_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	unknown	unknown	gnl\|CDD\|178810

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_007051524.1\|297558_297948_+\|chorismate-mutase	gnl\|CDD\|181719	PRK09239, PRK09239, chorismate mutase; Provisional.	9.5939e-49
NZ_CP013673.1\|WP_007051537.1\|282924_284328_+\|DNA-recombination-protein-RmuC	gnl\|CDD\|376878	pfam02646, RmuC, RmuC family. This family contains several bacterial RmuC DNA recombination proteins. The function of the RMUC protein is unknown but it is suspected that it is either a structural protein that protects DNA against nuclease action, or is itself involved in DNA cleavage at the regions of DNA secondary structures.	1.4062e-106
NZ_CP013673.1\|WP_007051520.1\|304846_305533_-\|endonuclease-III	gnl\|CDD\|223255	COG0177, Nth, Predicted EndoIII-related endonuclease [DNA replication, recombination, and repair].	2.51632e-96
NZ_CP013673.1\|WP_007051530.1\|287932_289432_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	gnl\|CDD\|235489	PRK05477, gatB, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB.	0
NZ_CP013673.1\|WP_003828150.1\|290802_291117_+\|DUF2469-domain-containing-protein	gnl\|CDD\|313765	pfam10611, DUF2469, Protein of unknown function (DUF2469). Member proteins often found in Actinomycetes clustered with signal peptidase and/or RNAse-HII.	1.30549e-58
NZ_CP013673.1\|WP_058101885.1\|293362_294976_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|235967	PRK07208, PRK07208, hypothetical protein; Provisional.	0
NZ_CP013673.1\|WP_007057703.1\|303258_304725_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173859	cd08494, PBP2_NikA_DppA_OppA_like_6, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP013673.1\|WP_007051540.1\|278941_279676_+\|aquaporin-family-protein	gnl\|CDD\|223653	COG0580, GlpF, Glycerol uptake facilitator and related permeases (Major Intrinsic Protein Family) [Carbohydrate transport and metabolism].	2.56303e-80
NZ_CP013673.1\|WP_011068470.1\|291323_293144_+\|histidine-type-phosphatase	gnl\|CDD\|132717	cd07061, HP_HAP_like, Histidine phosphatase domain found in histidine acid phosphatases and phytases; contains a His residue which is phosphorylated during the reaction. Catalytic domain of HAP (histidine acid phosphatases) and phytases (myo-inositol hexakisphosphate phosphohydrolases). The conserved catalytic core of this domain contains a His residue which is phosphorylated in the reaction. Functions in this subgroup include roles in metabolism, signaling, or regulation, for example Escherichia coli glucose-1-phosphatase functions to scavenge glucose from glucose-1-phosphate and the signaling molecules inositol 1,3,4,5,6-pentakisphosphate (InsP5) and inositol hexakisphosphate (InsP6) are in vivo substrates for eukaryotic multiple inositol polyphosphate phosphatase 1 (Minpp1). Phytases scavenge phosphate from extracellular sources and are added to animal feed while prostatic acid phosphatase (PAP) has been used for many years as a serum marker for prostate cancer. Recently PAP has been shown in mouse models to suppress pain by functioning as an ecto-5prime-nucleotidase. In vivo it dephosphorylates extracellular adenosine monophosphate (AMP) generating adenosine,and leading to the activation of A1-adenosine receptors in dorsal spinal cord.	3.0389e-06
NZ_CP013673.1\|WP_011068473.1\|286062_286362_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	gnl\|CDD\|178810	PRK00034, gatC, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC.	3.21183e-29
NZ_CP013673.1\|WP_058101884.1\|295181_297251_+\|transcription-termination-factor-Rho	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	0
NZ_CP013673.1\|WP_007051535.1\|285047_285896_+\|RNA-methyltransferase	gnl\|CDD\|349969	cd18096, SpoU-like, SAM-dependent rRNA or tRNA methylase related to SpoU. RNA 2'-O ribose methyltransferase catalyzes the methyltransfer from S-adenosyl-L-methionine (AdoMet) to the 2'-OH group of ribose in tRNA or rRNA. It is part of the SpoU family of MTases, a subfamily of the SPOUT methyltransferase superfamily. The SPOUT methyltransferase superfamily is a large class of S-adenosyl-L-methionine (AdoMet or SAM)-dependent RNA MTases which are structurally characterized by a deep trefoil knot.	4.64827e-41
NZ_CP013673.1\|WP_007054751.1\|286365_287907_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	gnl\|CDD\|234572	PRK00012, gatA, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA.	0
NZ_CP013673.1\|WP_007051542.1\|277028_278708_+\|phosphoenolpyruvate--protein-phosphotransferase	gnl\|CDD\|224006	COG1080, PtsA, Phosphoenolpyruvate-protein kinase (PTS system EI component in bacteria) [Carbohydrate transport and metabolism].	0
NZ_CP013673.1\|WP_011068468.1\|300379_303220_-\|valine--tRNA-ligase	gnl\|CDD\|380147	NF000540, alt_ValS, valine--tRNA ligase.	0
NZ_CP013673.1\|WP_007051538.1\|282579_282861_+\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|224848	COG1937, COG1937, Uncharacterized protein conserved in bacteria [Function unknown].	2.43596e-30
NZ_CP013673.1\|WP_011068472.1\|289754_290792_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	8.65156e-13
NZ_CP013673.1\|WP_007051539.1\|279759_282468_-\|HAD-IC-family-P-type-ATPase	gnl\|CDD\|319774	cd02079, P-type_ATPase_HM, P-type heavy metal-transporting ATPase. Heavy metal-transporting ATPases (Type IB ATPases) transport heavy metal ions (Cu(+), Cu(2+), Zn(2+), Cd(2+), Co(2+), etc.) across biological membranes. These ATPases include mammalian copper-transporting ATPases, ATP7A and ATP7B, Bacillus subtilis CadA which transports cadmium, zinc and cobalt out of the cell, Bacillus subtilis ZosA/PfeT which transports copper, and perhaps also zinc and ferrous iron, Archaeoglobus fulgidus CopA and CopB, Staphylococcus aureus plasmid pI258 CadA, a cadmium-efflux ATPase, and Escherichia coli ZntA which is selective for Pb(2+), Zn(2+), and Cd(2+). The characteristic N-terminal heavy metal associated (HMA) domain of this group is essential for the binding of metal ions. This family belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	1.26045e-151

>NZ_CP013673.1|WP_007051530.1|287932_289432_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB
MAEKLMKYADATKKYDVVFGLETHVELSTNTKLFCPAHIEFGGEPNTELTPVSLGLPGSLPVINKTAVDYAIKLGLALHCEIAEWSQFARKNYFYPDMPRDYQISQYDKPTNGNGYLDVELEDGTVFRVPIERAHIEDDAGKNTHVGGADGRIEGADHSLVDYNRAGVPLIEIVTKPIEGAGDRAPEIAGAYVRAIRDIVRALNISHARMEQGNMRADVNVSLRPSPDAPYGTRSETKNVNSFRGIEKTIQYEIRRQAARLDDGKEILQETRHWDEATQTTAGGRLKSDADDYRYFPDPDLVMLHITKEHIEEMKAQMPEMPRERRNRLKSEWGLSDLQMRDILNADALDLIEETVKAGAKAAGARKWWLGELSREANAKGVSLEELPITPADVAEVEKLIASGKLNDKLAKQTVEGVLKGEGTPDEVVKKHDYKIVEDNGAIEAAVDAAFEANPDVVEKLKSGNMKPMGVIIGAVMKATRGQADAKAVTKVVMGKIKG
>NZ_CP013673.1|WP_007054751.1|286365_287907_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA
MSNETATLVKLSAAEQAAAVKKGDVTSRELVEAHLKVIEAAEPSIKAFLKVSGDVALEQADAFDAKSAEDKAALPELAGVPIAIKDMIVTKGIETTAASKILEGWVPPYDATVIEKLKAAGMPILGKTNLDEFAQGSSTEHSAYQTTHNPWDTERVPGGSGGGSASAVAAFEAPIALGTDTGGSIRQPGALTGTVGVKPTYGGVSRFGAIAMASSLDQIGPVSRTVLDSALLQEIIGGHDKRDSTSIPEGPRPMVAAAREGAKRDLKGMKVGLIKELGGDGFQPGVEARFNEAVDKLKEMGAEVVEVSVPHIGYSLGAYYIIMPSEVSSNLARYDGMRYGLRVMPPTGVPQTAANMMAYTREAGFGDEVKRRIILGTYALSAGYYDAWYGSAQKVRTLIIEDFKKAFEQVDVLVAPTSPSTAFKFGEKMDDPLAMYMNDIATIPANLAGVPAMSIPAGLSDDGLPVGFQFIAPQQRDEVMYKPAAALEAALEDSWNGPIWNDLKTPWLDGLGK
>NZ_CP013673.1|WP_011068473.1|286062_286362_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC
MPTFSREEIVHLGDLARIALTDEEITRLQGELNVIADSINKVQEVASDDVPPTANPVPLEAYLRPDVAETPLTQEEALAGGPKTEAGMFVAPRILGSEE
>NZ_CP013673.1|WP_007051535.1|285047_285896_+|RNA-methyltransferase
MHAPNQISLAAKASGEPEFREIGLGPWSETHPGEPRPDDPTSSNYDGRFDSVLLNDGDRRNVLDRYRYWTVAAIKADLDARGRHDFEVAVENWTHDFNIGSMVRTANAFQAKRVHIVGPHKWNRKGALMTELYQHVEHHPSIAELVESWHHRIAGEIAYERAKAGAAAIHAHDVAVDGDNKHLHELLAEIDACDARIKELQAARVIALDIIPGAVPMEAYAFPKRCLLLFGAEGPGLSEKALALADDVVYISQFGSVRSINAGAAAAVAMHAWIAQHAVSGV
>NZ_CP013673.1|WP_007056499.1|284396_284954_+|hypothetical-protein
MLEPREQLATLLKEHVVGRPFSELAAVTFDHRAATVMGHVLIDALEDAGYSIDDFDAVGALTAASVPMVSAMIQAAASRGEDLDGFVMDFVYPSIKGPSIEGRRVVLLDAWLSEKSYVQTSSLVTLRNGNELSLDFGIVEQLGAKVVAIASLVGGGAKDINVVNPSTGDEQTLPFIQVFDESELR
>NZ_CP013673.1|WP_007051537.1|282924_284328_+|DNA-recombination-protein-RmuC
MIIVIVVLVVGAGLGLFAGFVLGRHKGQEMARGVKSEELEEAKTSLENARFENAELSARNAAAQAQIEGVNQQLAFAKSQLAQAQQAEQIRIQQERERAAAEAERKRQADAQAAEAKRAEQEARLKEQSKVLEALAPVAKNLDTLQNKVTQIEEGRKREMGALGAQLKGLNDQQARLDKETSSLSAALRNNKVRGAWGEAQLKNIVESAGLLEHVDFDTQVVVTDADGRTLRPDMIVHLPGGKTIPIDAKVPYADYQRACEIPDTASPEDIARRDDLLRSHAKALREHVRALGEKAYWNAFDVAPDFVVAFIPNEALLQAALEADPTLMDDAFSRKVALTSPVTLWAVLKSVAYAWQQQSLTDDAKQLFDLSRELYERFSTLGDYAIKLGTQITKTVSAYNKFASSLERRVLPTARKLQKIEPTKIIEEVPIIESDKGNVSELSAPEVVPADEGDTHLTASGDSLES
>NZ_CP013673.1|WP_007051538.1|282579_282861_+|metal-sensitive-transcriptional-regulator
MHGYDEDKAKVIARLRRIEGQVRAITQMVEDDKYCIDILTQISASNSALKSVALLLLDDHLNHCVRQASIQGGEVADEKLAEASAAIARLVKS
>NZ_CP013673.1|WP_007051539.1|279759_282468_-|HAD-IC-family-P-type-ATPase
MELSIFSAATALIAAAALTWLVLRFFFGTQKATAGAMDASGERQSATITVKGGYSPAVISMRTGTPITLTFDRQETGECTSHVVFADLGLDAMLPGNATTDVELPALPAGEYPFACGMNMVHGLLRVEGEESKDGADKDGLRPRADGSAEAEGVSPSDLRVGAPVVDAAEAERREAAERANEIKALTKLVIVGAVLTLPVFAVTMLHMANPALVPHWMVNPWLQAILITPVMFYCGRPIHTVGFPALAHRSPDMNSLVSLGTSAAYLYSLVTCIAPWVFPEGSREPYFESVGVVITLVLVGRLLEAKAREGTGKAVQSLIRLRPRTAHKLNATSADNVDGIEWRNPAHFTDTDIDAIVTGDLLIVKNGERVPTDGVIVAGEARIDESMITGESKPVSKTAGDPVTGATVLLKGDCVMRATQVGADTVLSQIAAMVARAQATKAPVQQLADKIARYFVPAVMIIAIWTFAIWVSLGPAPQLAHALVTAVSVLIIACPCALGLATPLSVTVSLGLGATNGVLVTSAKALEQARRIGTVVFDKTGTITRGVVDAAADWDKPSYEQDTVKEGSREAVAALRARGIRTVMLSGDKAEVAGRIAREVGIDTVICEVKPDGKAYWIAKLQRERDEAAAKSAYGTSRTAAQSRTLIAMVGDGINDAPALAQADLGIAIGTGTDVAMQSADVTLMSGDLRGVIKTINLSNATMRNIRENLGWAFGYNVIGIPVAAGVLYPFTGWLLSPMIAGLAMALSSVCLVLNANRLHGANINVGAADGPAGSGSSTADVESAGSAESANAANITGSATSNAPHEPTVIIDDRTTLNQTNHVSDQSNNPTNKENTMDTGMHMHHTAPADGETATDPVCGMTVAVNADAITREYEGKSYYFCGEHCATNFMKAPQVFLEQ
>NZ_CP013673.1|WP_007051540.1|278941_279676_+|aquaporin-family-protein
MDYPLFTKLAAEFFGTAILMIFGNGSVANVELKNTKGHHAGWLNIAMGYGFGVMFPVLMFGSVSGAHINPAMTIAQAVNGLFPWSDVLPYIVAQLLGALLGQLIVYITYYPHYKETEDAEAILGTFCTTDADNQKVNYFLNEMFGTLVLVFGALCCLSLAWGKQDYAAASIVVGFIVWGLVTSMGGPTGPGLNPARDLMPRLLHAILPIPHKGSSRWGEAWIPVVAPIVGAIIGAWLFVFFFAS
>NZ_CP013673.1|WP_007051542.1|277028_278708_+|phosphoenolpyruvate--protein-phosphotransferase
MRTIQGVSVSAGIAIGTVRVLAAVDYAVERRLIDDPQAEMDRFRAARDTAVAQLKQLRDNVAAEFGENKAELFDAHRLMLQDPDYAECVEGLIAQDKVNAEFAVKSAAEQFAAMFAAMDSSTMQARAADVKDVSRRVMNVLQGKRDSTAQDGSVQGDAVQNGIVQNGIAQNGESHIIFAEDLAPSDTAQLDRAKVLGLVTAKGSANSHTAILARTMGLPAITGIGDAFDPADDGHVAVIDGTSGAVFVDPDEATLTEYRRRKAEAEEHLSLLRKLKGKPTETKSGQRVHLYANISRPSDAAAVLANDAEGIGLFRSEFLYLEREDWPTEEFQFDAYGQVAQEMGDRPVIIRTLDIGADKQVDYFNLSHEDNPALGYRAIRICLTRPEIFKVQLRALLRASAYGNIAIMLPMITSVQEVRDAKRILEEAKSELRGERIDFNESIQIGVMIETPASVIMADELAAEVDFFSIGTNDLTQYTLACDRQNPSLERFADPHSPAVLRMIQMTIEAAHRHGIWCGICGELGADLSLTDTFLRLGIDELSVSPTSVLPLRNVIRNH
>NZ_CP013673.1|WP_011068472.1|289754_290792_+|GNAT-family-N-acetyltransferase
MATEAQLKRDLPQSIVIPPIRGEMVHLRPATVEDLPRLDELDAFYGASKITGKDAVTERAIVHTWVRRSQAWEAGQAPAESGVGDPESRRTIAWAVLTDADHDDDGQLDAASTDNVIGMIFLIDIDGWSKSARIQIILGREYRGRGYSRDAMPRVMTYGFAPEPAGLGMHRIWVSVPEKNSRSISVYQSLGFVPSGTSRDALWDAENNKYQDLIVMDTLADEYDPIRSLDAFGMHLIEDNPGVKEALSAREHSIAIQQNKPEPEPAQRGEAAGATTSDVQSQAQTPAAAQPVEPQAEHHDDTQKNTRHSLEEESNWPYGQAERKPSKEAWWRTLGRGRKRDTESE
>NZ_CP013673.1|WP_003828150.1|290802_291117_+|DUF2469-domain-containing-protein
MSAEDLDNYETDAELALYREYRDVIKLFTYVVETERRFYLANKVDFNVRSAGQDVYFDVQLTDAWVWDVYRSSRFVKSVRIVTFKDVNVEEVQKTDIDIPDDIH
>NZ_CP013673.1|WP_011068470.1|291323_293144_+|histidine-type-phosphatase
MVAAATLLAGGILTVPHAMALEADGQYYSSKQPYVAPSEATTASYSQAPEGYETVYTESMARHGSRGLSSYKYDALLMKMAEAAEADNGFKSDAIKSEFMKNLKAITAANVENGYGMLTGQGADQHQGIGARAYERNKTLFDNAAKDGGKIAYQSSGEARATESGENFARGFNAASNNKLANSTVTPADPAGTGEAAAFDKTPNTLYFHKSENPDGTEKTGEAKQRADDYQNFVENDAIIAGAEQTIAENEDVKTASHDLLSQIFTDDFLAKLADGTYAWYNTVDGTKGGEANCAPGADPSKDADACGAAKKKIASEYDAAMDLYNLYIIAADMENENTGSHTFDFNQYFQGEQADDAKLFAWALDAEDFYEKGPSYAGQDETYTIAQPLLDDFFSSIDERVNGGSTVATFRFAHAETMMPFAALLGLPGSTQQAAASTTDVYTYANNEWRGESVTPMAANVQWDVAVKSGNDPKTGRAYTPLVRMLYNEQEIAFRSECTPIADGSTWYKLTELKSCLASDHQTLGDDAHLTDDSTTQPGTGPNTGEGTSTTPNNNGAGTHQPSNTQANGTENELSRTGVAVTGVAGIMMLLALAGISLNLWKVRR
>NZ_CP013673.1|WP_058101885.1|293362_294976_+|NAD(P)/FAD-dependent-oxidoreductase
MTDKQSVVIIGGGPAGLTAAWELIKDGGADKYDVTVLEGTREFGGISRTVKHNGNRMDIGGHRFFSKDERIMDWWKTVLPLQGAPSYDDKKLGRDHDMEPGGPDPETEDKVMLKRHRVSRIFWNRHFFDYPISLSPNTLKAMGFKLTMVAGFSYLKSMFHKLPEDNLENFYINRFGRKLYSMFFEGYTEKLWGRHPSQISADWGAQRVKGLSIMGVLKNAFQKLLPKKRSNAEVETSLIEEFWYPKYGPGQLWETVESNCEAAGVKVLTDARVVEVRQTDGAVSSVVYEDSEGNRTELSGDQFISSMPVKDLVNAIDAAGADPEAVDSKPAPADMTEVANGLPYRDFVTVGLLVKHLKLKNTTSIPTLGDPPIVPDCWIYVQDPGYKVGRLQIFNNWSPYLVKDVDDTVWIGLEYFCEEGDSFWNMSEEDVTKFAISELTRMRVINGPDEVIDSHRERVRKAYPAYFDTYEHMDELIEYLDGFGNLYCVGRNGQHRYNNMDHSMATAMEAVGNIKTGKTSKKNVWSVNTEKSYHEEK
>NZ_CP013673.1|WP_058101884.1|295181_297251_+|transcription-termination-factor-Rho
MANSQNLEDMKLPELKELAKQMGLRGTSTMRKPELLATLQAARNGGEPPAGVTVRAPKAAKTAKVVKAPQSDAAEANTTDNADVATQSPAPAPAATEPQLDLPLPVADDAKKDETEPRRTRRKAADDAASEPRAARRRRDDDQPDFARRKPRKKADEAGDLLATLDLGDAAPTERRRERHEDVEVPLIRRVRDDEDEQPHRRRRTAENSEETVRDLDDILATLPTQKHEETSEDGEQNDDHEFVRRNRRDRSDRNDRDTRNDRSDRRNRRMRGRDRDNADDDRRYDDRDNRSDRNDRDSRREEPQEDLVPVAGIVDVLDSYAFVRTSGYLPGPNDVYVSMGQVKKYGLRKGDAVHGSIRAPREGDRRNQRQKFVPLQAIDSINGQSVEEALNRPQFSKLTPLYPQERLKQETAPNKLTGRIMDIVSPIGKGQRGLIVSPPKAGKTITLQNIANSIAANNPEVHLMVVLVDERPEEVTDMERTVQGEVISSTFDRPASDHTTVAELAVERAKRLVELGQDVVVLLDSMTRLARAYNIAAPASGRILSGGVDAQALYPPKKFFGAARNIENGGSLTIISSALVETGSKMDEVIFEEFKGTGNMELRLSRELADKRLFPAIDINASGTRREELITNPQELPIIYRLRRLLGGMEPEQAYQTLVPRLKKTATNRDFLAAIVQQANTGNAVNGN
>NZ_CP013673.1|WP_007051524.1|297558_297948_+|chorismate-mutase
MSETSSDWQRTTIDSAQAAAHPETAQAVARIKALRQTIDNIDSAVIALLAERFKATSQVGVLKANAGFAPEDTKREDYQIERLHRIAIDAGLDPEIAEMYREFVVTEAKKRHQRIADAGGDPGVLDVFA
>NZ_CP013673.1|WP_013582355.1|298069_300154_+|hypothetical-protein
MRCGAALVSCALCVASILGGAWMSRPTPVDYGPVLATASDMYAVTDAEGEPVRWYVVGKGGAGNGASADSGNSGSTDTDSANSNSGTSKVSRIPASAATLPWKVSVTYSLDGPNVEANEVAGASGLIGVYIDIKPQTKEANRTIPVVAFTVPTQVADDVSADNSITVTTQGSNTVVAAAGKAATGLEFSCYMNAKDFSMSSVALAVLPSNSSSPAVGANPDAANAANAAAQPAADTDVAQLTASAATLVDSLTDAGSGEQQQLIEQLQTLRDNERALNKSVVAERETAHKRTFEDYMAAYVGSYTTHLSGSIGTSTQLPALMGTAGELSGDTPLAQAVLDLANAVNNVSAAHQHAGAVDALDEVIRRIQQQGTTGLVDDLIAEASEEATQGSKQYADGQSQLSAAMIPYSMKYTDVYTANLSALTGGTSSGATAYESQAIAETNGSDELADAQSKVDAAMSTLATASEHTGKATALRQIVLRFSDQFEGGASSASGSDGDGSSGDVSSDPVTEAQALTGLVDSQSQSFYGKTRVAQAKRKADAARKQAKAAQQQQSQHSKASLVDDTMSMSAGDVMNYAGGLTSAIGGGDKSDSSKSAGSGTNDSAKSSDTGDSGNGKASNASDSGNNLDTAPVLFGFGTGGTLFKHDMNALINETVKISDAGTLLAQAVAQLDSPNTQQKTAETRYLIVIPTV
>NZ_CP013673.1|WP_011068468.1|300379_303220_-|valine--tRNA-ligase
MAHYRSIVRTSPANSLLGCLLYSSACHATCINFGLMTEGKSIINANLTPLPDKVGVDGLEDKWRTVWDEDGTYKFRNTRDRKAVYSIDTPPPTVSGSLHVGHVFSYTHTDVIARYKRMRGYDVFYPMGWDDNGLPTERRVQNYYGVRVDVSLPYDPDFKPPFEGTDGKKIDAKDQVPISRKNFIELCERLTAQDEKLFEALWRKLGLSIDWSQTYHTIGQHPQRVAQKAFLRNLARGEAYQQDAPGLWDVTFQTAVAQAELESREYPGFYHKVAFRFEDGTPIYIETTRPELLAACTSLIANPNDERYKQYFGQYVYSPLFKVKVPILAHPAAEMDKGAGIAMCCTFGDVTDVEWWRDLKLPTRPIIQRNGRIVMDTPDWIEDPAGREVFAETAGKTTFSARKIIVDKLRESGDLDGEPTPTKRMTNFYEKGDKPLEIVTSRQWYLKNGGTDAKLNAELIERGKELEFHPDFMRVRYENWVHGLNGDWLISRQRFFGVPFPLWYPVNASGEPDYDHPITPSEDRLPIDPTIDVPEGYDESQRDVPGGFTAEKDIMDTWATSSLTPQIVTHWAEPDEASKALFASTFPMDLRPQGQDIIRTWLFSTVDRAHLENKCLPWAHATLSGWILDPDHKKMSKSKGNVVVPNEPIEKFGADAVRYWAAAARLGLDATYDIGQMKIGRRLAIKLLNATKFALAIGREDENHHVGAAAEAAWNPADVTEPLDRAAMAKLALVVRQATEALESYEHSKALEVIESYFWQFCDDYIELVKNRAYGTPDEHGNVPSEKAVKSARTALGLGLDAFARLLAPYLPYATEEVWSWMHAGSGSVHRAAWPVVDPYVEAATGASPELLTWAGKAVEQLRKIKSEAKVSMKTPILSVALSAASEGVEAIHAALGDIAQAGRVVGKFDLVAKHAEESAAEGTPETEVAVEASELGEPPAKKPKH
>NZ_CP013673.1|WP_007057703.1|303258_304725_-|ABC-transporter-substrate-binding-protein
MALGALVVVGWTFMQNRFQPGSSLDADVTIGIDDMPQSLDIRSDSSAAAERLLVDNVYETLVTVDQDNKLQPGLATSWKTSDDGLTVTLTLQSGVTFSNGHTLDASDAVWSLQQNVTNKVADVDELGDLASVANPNATTVVITLAKPNPTLLRALSGRLGIVYDSESSSADYQRKAIGSGPFTVADFQPGHSLKLARSDTYHGTKAASNVVEFMQYSDADALSKALTDGSLDMAAPVSASTATGLNGKDGLTVKEGATTDKVLLAYNNGTDSLLSDEQARKAFRYQIDAAGIASAQPDAAGALGGPISLLEPGYEDLTGLYPHDENQAGQMFSYFGAQYLTTVNLVVPEEYRSLAETIKQQIERQPRPTVNLEVLSDEDYAKRIKDGKWELTVMSMDGTDDAGIFADPDSMFHYDHTEAQQAYADARAATNDADYEARMKAYARLISEDAASDWLYTRKCFTVASTKVSGYPTSMINRRMPLAGLTVK
>NZ_CP013673.1|WP_007051520.1|304846_305533_-|endonuclease-III
MRETKSARLTRMHDEYDILRQVIPAPACALHFSNPLELLIATVLSAQTTDKRVNTVTPELFATYPTARDLAAANPAQVEDIIHPLGFYRSKTQHLIGLATALDERFGGVVPRTMDELTSLPGVGRKTANVVLGNAFDIPGFPVDTHVMRVTGRLRWRSDWRSAHPDPVKIEKEITSCFPPEEWTNLSHRLILFGRATCHARTPDCANCPLSDTCPSYAPPAGKSTSKR

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Crispr_ID: NZ_CP013673_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_3

881726-881806

Orphan

Consensus_repeat	Method
ATATGAGACGGCTTCACTGTGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013673_3

>merge|NZ_CP013673|3|881726-881806|CRISPRCasFinder
ATATGAGACGGCTTCACTGTGCGTGGCTGCAGGTAGAGACTGCCCGCGCGGCGGCGACATATGAGACGGTTTCACTGTGCG

>NZ_CP013673|3|3|881726-881806|CRISPRCasFinder
ATATGAGACGGCTTCACTGTGCG	TGGCTGCAGGTAGAGACTGCCCGCGCGGCGGCGAC
ATATGAGACGGTTTCACTGTGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_058101849.1\|888648_890202_-\|UDP-N-acetylmuramoyl-L-alanyl-D-glutamate--2,-6-diaminopimelate-ligase	unknown	unknown	gnl\|CDD\|234660
NZ_CP013673.1\|WP_007054436.1\|891715_892660_-\|aldose-1-epimerase-family-protein	unknown	unknown	gnl\|CDD\|185699
NZ_CP013673.1\|WP_058101847.1\|895063_895573_-\|Cys-tRNA(Pro)-deacylase	unknown	unknown	gnl\|CDD\|237976
NZ_CP013673.1\|WP_007054435.1\|891128_891449_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007052568.1\|875745_877455_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224048
NZ_CP013673.1\|WP_058101850.1\|883735_887413_+\|chromosome-segregation-protein-SMC	unknown	unknown	gnl\|CDD\|274008
NZ_CP013673.1\|WP_058101853.1\|870118_871396_+\|N-acetylglucosamine-6-phosphate-deacetylase	unknown	unknown	gnl\|CDD\|238434
NZ_CP013673.1\|WP_032684937.1\|871675_873310_+\|peptide-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173884
NZ_CP013673.1\|WP_058101851.1\|882079_883675_+\|dihydrofolate-synthase	unknown	unknown	gnl\|CDD\|223362
NZ_CP013673.1\|WP_010080884.1\|878074_879670_-\|aminopeptidase-P-family-protein	unknown	unknown	gnl\|CDD\|238520
NZ_CP013673.1\|WP_007052562.1\|867788_868913_-\|ROK-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224851
NZ_CP013673.1\|WP_011068010.1\|893965_895024_+\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	unknown	unknown	gnl\|CDD\|234893
NZ_CP013673.1\|WP_011068008.1\|890319_891129_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|236608
NZ_CP013673.1\|WP_007057255.1\|877504_878026_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240032
NZ_CP013673.1\|WP_058101852.1\|873479_874571_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223674
NZ_CP013673.1\|WP_007052567.1\|874572_875742_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP013673.1\|WP_058062661.1\|869250_870063_+\|glucosamine-6-phosphate-deaminase	unknown	unknown	gnl\|CDD\|179028
NZ_CP013673.1\|WP_007055266.1\|887531_888527_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379214
NZ_CP013673.1\|WP_058101848.1\|892784_893741_-\|aldose-1-epimerase-family-protein	unknown	unknown	gnl\|CDD\|185699
NZ_CP013673.1\|WP_032747016.1\|879973_880954_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_058101849.1\|888648_890202_-\|UDP-N-acetylmuramoyl-L-alanyl-D-glutamate--2,-6-diaminopimelate-ligase	gnl\|CDD\|234660	PRK00139, murE, UDP-N-acetylmuramoylalanyl-D-glutamate--2,6-diaminopimelate ligase; Provisional.	1.39677e-149
NZ_CP013673.1\|WP_007054436.1\|891715_892660_-\|aldose-1-epimerase-family-protein	gnl\|CDD\|185699	cd09022, Aldose_epim_Ec_YihR, Aldose 1-epimerase, similar to Escherichia coli YihR. Proteins similar to Escherichia coli YihR are uncharacterized members of aldose-1-epimerase superfamily. Aldose 1-epimerases or mutarotases are key enzymes of carbohydrate metabolism, catalyzing the interconversion of the alpha- and beta-anomers of hexose sugars such as glucose and galactose. This interconversion is an important step that allows anomer specific metabolic conversion of sugars. Studies of the catalytic mechanism of the best known member of the family, galactose mutarotase, have shown a glutamate and a histidine residue to be critical for catalysis; the glutamate serves as the active site base to initiate the reaction by removing the proton from the C-1 hydroxyl group of the sugar substrate, and the histidine as the active site acid to protonate the C-5 ring oxygen.	9.47287e-132
NZ_CP013673.1\|WP_007052568.1\|875745_877455_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP013673.1\|WP_058101850.1\|883735_887413_+\|chromosome-segregation-protein-SMC	gnl\|CDD\|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0
NZ_CP013673.1\|WP_058101853.1\|870118_871396_+\|N-acetylglucosamine-6-phosphate-deacetylase	gnl\|CDD\|238434	cd00854, NagA, N-acetylglucosamine-6-phosphate deacetylase, NagA, catalyzes the hydrolysis of the N-acetyl group of N-acetyl-glucosamine-6-phosphate (GlcNAc-6-P) to glucosamine 6-phosphate and acetate. This is the first committed step in the biosynthetic pathway to amino-sugar-nucleotides, which is needed for cell wall peptidoglycan and teichoic acid biosynthesis. Deacetylation of N-acetylglucosamine is also important in lipopolysaccharide synthesis and cell wall recycling.	2.2623e-145
NZ_CP013673.1\|WP_032684937.1\|871675_873310_+\|peptide-ABC-transporter-substrate-binding-protein	gnl\|CDD\|173884	cd08519, PBP2_NikA_DppA_OppA_like_20, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP013673.1\|WP_058101851.1\|882079_883675_+\|dihydrofolate-synthase	gnl\|CDD\|223362	COG0285, FolC, Folylpolyglutamate synthase [Coenzyme metabolism].	1.55329e-130
NZ_CP013673.1\|WP_010080884.1\|878074_879670_-\|aminopeptidase-P-family-protein	gnl\|CDD\|238520	cd01087, Prolidase, Prolidase. E.C. 3.4.13.9. Also known as Xaa-Pro dipeptidase, X-Pro dipeptidase, proline dipeptidase., imidodipeptidase, peptidase D, gamma-peptidase. Catalyses hydrolysis of Xaa-Pro dipeptides; also acts on aminoacyl-hydroxyproline analogs. No action on Pro-Pro.	1.95254e-108
NZ_CP013673.1\|WP_058062661.1\|869250_870063_+\|glucosamine-6-phosphate-deaminase	gnl\|CDD\|179028	PRK00443, nagB, glucosamine-6-phosphate deaminase; Provisional.	1.6011e-124
NZ_CP013673.1\|WP_058101848.1\|892784_893741_-\|aldose-1-epimerase-family-protein	gnl\|CDD\|185699	cd09022, Aldose_epim_Ec_YihR, Aldose 1-epimerase, similar to Escherichia coli YihR. Proteins similar to Escherichia coli YihR are uncharacterized members of aldose-1-epimerase superfamily. Aldose 1-epimerases or mutarotases are key enzymes of carbohydrate metabolism, catalyzing the interconversion of the alpha- and beta-anomers of hexose sugars such as glucose and galactose. This interconversion is an important step that allows anomer specific metabolic conversion of sugars. Studies of the catalytic mechanism of the best known member of the family, galactose mutarotase, have shown a glutamate and a histidine residue to be critical for catalysis; the glutamate serves as the active site base to initiate the reaction by removing the proton from the C-1 hydroxyl group of the sugar substrate, and the histidine as the active site acid to protonate the C-5 ring oxygen.	1.14538e-125
NZ_CP013673.1\|WP_011068010.1\|893965_895024_+\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	gnl\|CDD\|234893	PRK01045, ispH, 4-hydroxy-3-methylbut-2-enyl diphosphate reductase; Reviewed.	8.39528e-163
NZ_CP013673.1\|WP_011068008.1\|890319_891129_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|236608	PRK09652, PRK09652, RNA polymerase sigma factor RpoE; Provisional.	1.73669e-71
NZ_CP013673.1\|WP_007057255.1\|877504_878026_-\|NUDIX-domain-containing-protein	gnl\|CDD\|240032	cd04676, Nudix_Hydrolase_17, 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 and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which 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.	1.36956e-55
NZ_CP013673.1\|WP_058101852.1\|873479_874571_+\|ABC-transporter-permease	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	3.33394e-104
NZ_CP013673.1\|WP_007052567.1\|874572_875742_+\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.94335e-82
NZ_CP013673.1\|WP_058101847.1\|895063_895573_-\|Cys-tRNA(Pro)-deacylase	gnl\|CDD\|237976	cd00002, YbaK_deacylase, This CD includes cysteinyl-tRNA(Pro) deacylases from Haemophilus influenzae and Escherichia coli and other related bacterial proteins. These trans-acting, single-domain proteins are homologs of ProX and also the cis-acting prolyl-tRNA synthetase (ProRS) inserted (INS) editing domain. The bacterial amino acid trans-editing enzyme YbaK is a deacylase that hydrolyzes cysteinyl-tRNA(Pro)'s mischarged by prolyl-tRNA synthetase. YbaK also hydrolyzes glycyl-tRNA's, alanyl-tRNA's, seryl-tRNA's, and prolyl-tRNA's. YbaK is homologous to the INS domain of prolyl-tRNA synthetase (ProRS) as well as the trans-editing enzyme ProX of Aeropyrum pernix which hydrolyzes alanyl-tRNA's and glycyl-tRNA's.	1.29417e-74
NZ_CP013673.1\|WP_007052562.1\|867788_868913_-\|ROK-family-transcriptional-regulator	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	5.7177e-37
NZ_CP013673.1\|WP_007055266.1\|887531_888527_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379214	pfam13480, Acetyltransf_6, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions.	6.65289e-09

>NZ_CP013673.1|WP_032747016.1|879973_880954_-|hypothetical-protein
MKTHKAVASLISAAQNELRCVYSRNEAEQTALRRRAQSGELLKVYDGIPSLYANTAYWDGLTPPERTLHMARALAQEHPQWVFGGLVAVSAYGFEHQWHLHDDCITIVTSDHGSRQCHQRLRHVYMPDMNNPKTHYEASGLSLISPARTLVEAAIDLDFRFALPIFDSALAKGITKEEIAADCVQWRIDYARVFRLLRYANERSENGGESLARGTIIEDRFLTPRIQVTVTDPQTNTEYRVDFVWKLDDGRVIVAEYDGTQKYVDPAMTDNRSIQEVVAKERARDEGLKRAGATEIVHFTYADVIERTPLRVKLIKAGVPQVETSA
>NZ_CP013673.1|WP_010080884.1|878074_879670_-|aminopeptidase-P-family-protein
MGEVITAKDKEYEAEERATAPGANQSMSDRVNNRSLRPQSAAFKEFMKSGWADDDPETNPLESSKFTPARLEALGKAFPGERLVIPAGQPKVRNNDCDYMFRPDTTFAYYTGLGSDYEAGAVLVLNPVDPDSPEAAAGKTHTPELFVAPRADNSTEDFFMSAHYGEYWVGPRAGLKEMQAMTGIETHDIAQLADALSKDVGAEAGAVRVRVVSETDPQITSMVESIREANGFADPDKNSASDDKLHEFAAEARMVKDGYEINEMRKAVDATKHGFDRLLSALPAALDKPRSERILEGAFNAVSRELGNAVGYDSIVASGPHAPILHWMRNTGVVKTGDMLLVDAGVEVDSLYTADITRTFPTNGKFTDFQKRLYQAVLDSQQAGFEAAKPGATYSDIHHACMRVIAERLHDWGLLPVSVEESLSPQGQQHRRWLACGVAHHLGLDVHDCAQARFESYQGAPIRPGMIFTIEPGLYFREDDLLIPPEYRGIGIRIEDDVLMTENGPEWISAGIPKQIDDVEAWMAEQAAQAK
>NZ_CP013673.1|WP_007057255.1|877504_878026_-|NUDIX-domain-containing-protein
MSTPEFVLELRKKIGHDLLWLNGVTGCVLNEHGQLLLGRRSDTGEWAMVYGINEPGEQPADTVVREIKEETGIDAIVTDLVAVTSSNKVLTYANGDNTMYMDHSFLCALKPGGNAEPFVGDEESLSVGWFDLDDLPTPLAASTSERLELFHTYIENKKHGDAHALFQFDGQQY
>NZ_CP013673.1|WP_007052568.1|875745_877455_+|ABC-transporter-ATP-binding-protein
MSENNKNLADIKDLSVSFMTDAGSIKAVEDVNFTIPRKTVVGVVGESGSGKSVTARSIIKLLPETATTSGAVYLSKRDGSDSLDVLSLSGEQLREVRGSEAAMVFQEPNSVLNPVYTIGWQIEEGLRAHGMKDKKELRAKAINILKKVGIPDAETRVDYYPHQFSGGQKQRIVIAMALVLNPGLILADEPTTALDVTVQAEILDLLRLARDEFDASVLIITHNMGVIADIADQVVVMYRGHVVEQGDVEQIFYHPKDDYTKRLLGAVPRIGQKLVVRDREGKPIERKADWREQPIAVEAKNLTITYPGHLMQPDFKAVDGANFTIHRSEVLGLVGESGSGKSTTGRAIAGLQKVSGGSLNVLGIEMNGVKERDFKPKRADIGFVFQDPGSSFNPLMTIAENVAEPLLVHHKYGSVADAKNYVGDLLEMVQLPRAYMNRFPHELSGGQRQRASLARGLALKPSLLIADEPTSALDVSVQAKVLELFKRLQAEIGFACLFITHDLAVVDMLADRIMVMHKGQIVEHGDADQIMQHPENPYTKKLLASLPVPDPREQQQHRAHLHELLAQEA
>NZ_CP013673.1|WP_007052567.1|874572_875742_+|ABC-transporter-permease
MTTASQDKITVPGDDRLTKLNVSTKTPFWTKIPIIKELRVAVGWQKGMLITGLAITAFFLLVALFAPLIAPYGHAQIKAADGTSFPAQAAPSAEHIWGTTAAGFDVFSRVVWGARTAVIAIVVAVLLSIFAGVLLGLVSGYYGGWVDRILVMIADAVYSFPSLLLAILMAIMISHGQSGLWSGILASGISITVVYIPQYFRTIRAEVIRIKESAYVESARVVGASTWRIMTKHLFKNSTRTLPVILTLNSSEAILTLAGLGFLGFGIEPTAAAEWGYDLNRSVSDVTAGIWWTAVFPGIAIVLIVLGITLVGESLNDLADPRLRARKSAGEVVGSIEDTSVDPNEKPTARNEVIAELDANVDPPATVTDHDPTIVASEWTGEGKPEGKE
>NZ_CP013673.1|WP_058101852.1|873479_874571_+|ABC-transporter-permease
MSDSAAATSSTTPAKAKTKKNRLSGSFFRFVLTRFLLIIPTVFILVTIVFFVMRATGDPISAALGGRLTPAELQQRIHAAGYDRPLIVQYVDYLGGLLHGDLGTTLTDNQPVISILTHYGAATFELAFLALIVALIVGIGLGRLAARKRDRAADAGIRTFAILCYATPVFFLGLVLKLIFAVWLNILPASGRSDLNSEMQFTRLVSPTGFYIIDAIQLGDMNVLVDVLRHAVLPAVALGLLTAGVFIRLVRTNVISTYNSGYVEAARSRGVSEKRLLNKHAWRPALIPIITVMGMQIALMLAGAVLTETTFEWKGLGFMLSQYLKARDFVAVQGIVILIAIIVAVVNFLVDVIAALIDPRVRY
>NZ_CP013673.1|WP_032684937.1|871675_873310_+|peptide-ABC-transporter-substrate-binding-protein
MNSKKILAAAVSVAAIASLTACGGVKDDTTAGADSGNAITIGTTDKITSLDPAGSYDNGSYAVQIQVFPFLYAQDYNTSELSPDIAADDGTWNDDGTEFTVKLKDGLKFANGNDLTASDVKFSYDRIKKINDPNGPSSLLANVESVTAKDDTTVVFKDSVPFDVTLKQVMSSPAGPIVDEDTFDADKLTDADTIVSKKAFAGPYTLTAFKINESAAYAKNDSYKGLTPAKNSAVQVKYFADASNLKMAVQQGQIDVANRSLSPTDIEDLSKDSKVKVVKGPGGEERFIAFNFKIQPYGESQPDADANKAKAVRQAVANLIDREELSTKVYKGTYTPMYSFIPDGLAGHDDTLKSAYGDGNGKPSTEKAKKVLADAGVTTPVDLKLQYNNDHYGSVSADEYAALKSQLEAGGLFKVDMQSTEWTQYNKDRVVTDDSDGVYPVYQLGWFPDYSDPDNYLSPFFRDGNFVNNGYSNKEVNDLIVKQAGEKDESARGDILKQIQKLETEDLSTIPLLQGAQVAVTGTSVKGVTLDASFRFRYASVTKG
>NZ_CP013673.1|WP_058101853.1|870118_871396_+|N-acetylglucosamine-6-phosphate-deacetylase
MSDRNEIVSRVTAALEGKPAPVAIRNARKVDACGERRGYWVVSDAAGVIVAAGTGEEAFEHYCRTVGLDPADRNAVIDAEGRILTPGYVDIHAHGAWEKSFDDGSDGIDVARAGHAVHGTTRQVLSLITNPVDVICRNIRTVRAKMESGRPDILGCHLEGPFLALARKGAHDPECLKDPVPDIVDDMLEASGAANGKIGCIRQITIAPELPHGISAIRQFAAAGVVPAVGHCDADYETAKAGFDAGAGIMTHMFNAMNGLHHREPGPIPAAVEDPRVTIELINDGFHVQDPMVSLSFRFAPHRTAFVTDAMAATDCPDGAYKLGALDVNVVDGHARLVSNGAIAGSTLLLEVAVRRAVCELGFSPVDAVEAATLTPAKAFGFDRPNPVTGAPIGLIAPGFAADFNLADPADWTVEQVWCAGRKLK
>NZ_CP013673.1|WP_058062661.1|869250_870063_+|glucosamine-6-phosphate-deaminase
MPEIIIVKNEAEAGEIYGRCVADLIKAKPDAVLGLATGSSPLAAYQALAKIVKDEAIDVSGVRGFALDEYIGLPLTHPESYHATIHRTVVEPLGLDPAKVHVPGDVLNGTPLEDGDKIALAGPAYDRAIEAAGGIDVQILGIGTDGHVGFNEPGSSLASGTRVKTLAEQTRIDNARFFDNDINQVPTHCITQGIGTIMKARHLVLLAFGAGKAEAIEETVEGGLSAFCPASALQMHPHATIIVDEEAASRLRHKDYYRYAYTHKPAWQGI
>NZ_CP013673.1|WP_007052562.1|867788_868913_-|ROK-family-transcriptional-regulator
MSYLGLNTTTDDHAAKASPADVRRKNRQLIFRLLFPTNQYSRAELGRRTGLSRVAVSDVVGRMLEEGLLRETGQAPSGGKGKRGTLLSIDIDRLRIISIDLTQEHLLHGAVTNLLGQPLRHAEVTLNTGSFVSVDVIIELIEKMLGMSDGEVIGIGVASPGVVDNGVVRSSTMRGWNNLDLSTPIAEHFGLEVNVSNDATAAMLTERFFGQGGPNMLFVRIERGIGSAILLSDTPVIGELHAAGELGHISIDLDGPPCPCGKHGCLETMISGTALKKQLSAADVEQHQNILARAGRYLGQALAMPVGLLDMADVCVYGQPNIINATFIGAAQQYLDAATSSSFHKHTVIRRCECGPDITVQGEAIAVVFQHLAK
>NZ_CP013673.1|WP_058101851.1|882079_883675_+|dihydrofolate-synthase
MRDVELDIMSRPPEHNTTNLDLDRMNLMLDILGHPEQSFRVIHITGTNGKGSTARMAEAICRAYGMRTGLYTSPHLEKINERIAIDGQQLSDDDFIDIWDQTKDLVALVDAKMEEQGKPKMSFFEVLTAMAIWKFADTPVDVAIVEVGMGGLWDATNVLNADAAIIGPVDMDHMQWLGDTVEQIATEKAGIIKPNCTAIIGPQPHEEAVMPILAEAAERNHAMLVRDGYEMTVSDRMAAVGGQVATLTTPNGTYEGVPIAKFGEHQAHNALAALAASEVVIPVNGPLDGDLVAEALSSVKIPGRIEQIRTSPTIILDGGHNVNAAEALRKAIEESYDFKQLVGVVAMMRDKQVEEYLGVLEPILSSVVVTENSWRERVMPADELEKIAVDVFGRDRVIKEANLPDAIQTAVNMVDAEDELGVGYGHGVLICGSFVTAGDARLMLEEHASPTMRQAMAVHQPAVDPDDSDQPADKAEDEAADNLEDSVSPDDFDVFDVLGLGKEQASDAGNAGTGTASADTGAVTDDSADVR
>NZ_CP013673.1|WP_058101850.1|883735_887413_+|chromosome-segregation-protein-SMC
MYLKELTLRGFKSFASVTTLRFEPGITAVVGPNGSGKSNIVDALIWVMGEQGAKNLRGTSMEDVIFAGTSSRPPLGRAQVSLTIDNSDHTLDIDYTEVTISRTIFRNGGSEYAINGSQCRLLDIQELLSDTGLGQQMHVIVGQGRLDAILKADPSGHRAFIEEAAGILKHRKRKERALRKLANTETNLSRLDDLLGEIHRQLGPLGRQARISRRADAIQISVRDAQARLYAEDAQRSMSRRDTVRQELGAVRNQLAVAQRELAQVKVRIEQVEALSSESSPAIAKANQYWHEFSQTRERLNALAQLAEERSRSLAGQIVTNFGEDPGMLVKRAEELESQAAAQTKAVADARIALDKATEERADDEKKLASVRQTLTELRKTAQERDAQIARLRELIAREESAVQLATSRAKDYASQRDSLTSQRDDAQQQLDALRSEADSIADDDGAALDAARATLAECRERLNERADKQREIQSKIISLKSKADALADTLDSRNASGSLERDTDVASLGRLTDFIHVAEGWEEAVAHALDQYASAIVVPAAGNMLHALERAREDKLGKAVVLTASIAGDPATEPGTESEESSAENAGAAPQSGNALAALVTANPDAENPAQSEAVVRTVRLLLADVAAAGTADEAQQIVAFGEAMRAVTKNGETFTHGVAAVGGSSISQSDLSLAARRDKALAQVKQLTAQDGGMAEQVAEAKTKRDEAARLVDQESAKRTEARLKAQQAEKSLKSATDRVASFTRQLEQLDRKITETQENCNEHQLKLDDLNRALASAQQSTAEHADFDELDERERTLERELNLTREHEVAAKIAWTEASRKGESLSRQAGLLRDNAKETAERRARIEALNDRRREQAAHLQGVADDARAVAAMVEHTLHDVAAKRDELQAAASSHDEELKALRAQRNQIEPKVTDLTGREHALDVNRERLAAESGQLMQKVSDELGLTLEELVSDYGPEQPVPVLDDEGNPVPLDETEAEAETEEGETGGETGTNGDSDRFKTVPYNRQEQKKRLDKARRDLAALGKINPLATEEFEALEERNKYLNDQRNDVVKSRDDLMQLIKDLDSTMVQVFKSAFDDTAEAFEQMFATLFPGGTGRLRLENPEDMLTTGVLVEASPAGKRVKQLSLLSGGERSLTALALLFAIFTARPSPFYVMDEVEAALDDVNLTRLINAFNELRAHAQLIIITHQQRTMSIADALYGVTMRADGVTAVVSQKLER
>NZ_CP013673.1|WP_007055266.1|887531_888527_-|GNAT-family-N-acetyltransferase
MITLEKVDGATLEAEAEKAGITLPIEQTKVWSGFQADIDGRTPWGDYLIKRDGELVAVISFIDFETHGYHYLRSMHGPAWVAKPTEAEEREVVDAIVDTVKKADKNIAFLRIDTWFADGTEKVLSTVPYDQTVVIDVTGGDDEILARMKRRGRRDVRKSLRECPAEVADETDKALADFSEYYDVMVETGQRDGFTPAPMSDYSDMIGALGADHCRVFAARIEDRVVAWSIVTVNGTHAVRYYAGMRNEVMRLHVTDKLLYSECCILGSQGITEYDLMGIGSDFAPSLKGLNEFKCKFTEEITPVAPARDVPIKKVFYKTLQTVQGVRKALR
>NZ_CP013673.1|WP_058101849.1|888648_890202_-|UDP-N-acetylmuramoyl-L-alanyl-D-glutamate--2,-6-diaminopimelate-ligase
MALTLASAADLLKEHHLLREIIQGDVWTDDPARIASADEPFAGITYDTRKVTPGTLLCCKGRFKAEYLNGIDEAGLAAYVAETEYSAATAAPGLIVNDARKAMSLLSAAFYGYPQNELTVIGVTGTKGKTTTSYFTQALINAVSGGKAALFSSVDNCLDGHTYVESDLTTPESMDAFRMMREAADNGMEYLVMEVSSQAYKVDRVYGLTFDVAAFLNISPDHISPIEHPTFEDYLYCKRQIIANAKSLVLGADSLHADLLREDAAAAGIGATTFALHDADNAGTSADVVAWPADPEHASFHIADGDQALGDYHLSIDGDFNYLNAAAAIAIAHAAGVSLDDADALHAIESVRIAGRMEQFRDPQSNTLAIVDYAHNYASVTALLDFVYERWGEENPRITLVTGSAGNKAYDRRKEIVEAAENRIANFIFTAEDTDTEPFIDICMEMQGYITNKDVASTVISDRPTAITNAIYDARAHADRFNILLIIGKGNERWIKDHHKHVPFDGDDHVVERMFGL
>NZ_CP013673.1|WP_011068008.1|890319_891129_+|sigma-70-family-RNA-polymerase-sigma-factor
MTTSEATMQSGQSAGSGESMAAKRARFEQLAMPAVNALYRQAMRLTNDPDDAQDLVQDTFERGFKAFDSFQPGSNFEAWMTTIERNAYFNQYAKAKRRPQRANDSTGEYDDWDIYDAAEHTSDGLKSAEEEYLDAFAPEEIMAALAKLSPERRQVFIDAAIDGKSYQQVADEQGVKIGTVMSRLNRARTQLKRELASYAKERGYVTGSSAGSPSAKLGENVGRIADSGHNGSSEQTVGSNGDTQAAVRHSHATGARTPQQSSKLSGKEI
>NZ_CP013673.1|WP_007054435.1|891128_891449_+|hypothetical-protein
MNDQPVERTRHISITRTGADGMVSQTEVHITAVHHRSVDTGSASASVQADVHIVTEGDCFDPRTCCDEREQALIAALRAYLRPDVAPECLIARLKATLDHCCGEDK
>NZ_CP013673.1|WP_007054436.1|891715_892660_-|aldose-1-epimerase-family-protein
MALKPRTGNQYVISSGEWSAVVTELGASLRELKWRGEDLIVPFDPNKVIPCCNGWVLAPYPNRVTNGQYSFDGEDYQMPIDEFDRQSSLHGYAYRYMWELVDLQESHVTLSWRSPDIAGYPFDITITATYALDENGLTETFTVHNNDSVKAPWAFGIHPWLANGKHATGQAITADNEPCRLELHCDTHVTVDEHLLPTGEEPVSGIFDLRDNPTLEGRGFDDAWTDITNRGEDGSTSAVFTRPDGIKVTLTGDKTINSWQVCTGNEIGEKARQAGVAVEPMTAYADAFRTGKDLVVLEPGDDYTTVVTFHAEQI
>NZ_CP013673.1|WP_058101848.1|892784_893741_-|aldose-1-epimerase-family-protein
MTSKTPRTGNQYSIHYGDYSAVICELGAKIRRFDYQGKEIFCPFGVNDLTPTCNGYVLAPWPNRIENGEYDFNGKHYCVPVNEYHPAPRNNANHGYAYHYMWKLESLTDSAVTLSLRFPNLDGYPFDVTVTVTYELGDNGMTATVNARNDGDEPAPWALGLHPWLANGKQGATAAERDADSAACHLQIKAASHVTVNEALIPTGTEPVTGIYDLNDGPTLEGRAFDDAWVDVERAADGTTTTTFTRPDGIEVKIIGDETINAWQCYTATGAPFAEHPYGIAVEPMTAPANAFRTGDHLVTLAPNGDYTTVVRYEVVQK
>NZ_CP013673.1|WP_011068010.1|893965_895024_+|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase
MTADSCNPCLTLENTIDVQEVPMTKSVVLADPRGFCAGVDRAILTVQTILKAAEASGKRTREDGLPPVYVRRQIVHNKHVVEDLAGQGAVFVQELAEIPDAAAQAGIPVVFSAHGVSPVVKAEAERRGMHVVDATCPLVGKVHREVLRFVREGYEIVYIGHKGHDEAVGVVGESPEHVHLIEHESDVDSLDFAPDTKLVLLSQTTLSVDETADTIAALKAKFPWIQEPPSSDICYATSNRQAAVKLVAQQSDCVVIVGSANSSNSVRLMEVAQEGLGERGKAYRVDDASELDPAWFEGLESVGISSGASVPDELVSGVIDALQNLGFTGMKSVETIKENMHFVLPAELRRKK
>NZ_CP013673.1|WP_058101847.1|895063_895573_-|Cys-tRNA(Pro)-deacylase
MAKKSKHDKGAGSTPATVQLEKAGVEFHVYEYEHSNDHMDDGYGVEAATKLGFDEHQVFKTLMADTGAERVVGVVPVSGHMDLKALAAAVGAKKASMADPKAAMRESGYVVGGISPLGQKTRHKTVLDESALQFDQILVSGGKRGLSVGVNPQDLLKVLNAVAAPIGTW

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Crispr_ID: NZ_CP013673_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_4

1566345-1566476

Orphan

Consensus_repeat	Method
GCGCAACATTCCCGGGAACGCGTCGC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP013673_4

>merge|NZ_CP013673|4|1566345-1566476|CRISPRCasFinder
GCGCAACATTCCCGGAAATGCGTCGCTCTGGACCCGAATCACACCCTCAAACGCGCAACATTCCCGGGAACGCGTCGCCACAGACCTCCATACACACGCCCACTTTGCGCAACATTCCCGGGAACGCGTCGC

>NZ_CP013673|4|4|1566345-1566476|CRISPRCasFinder
GCGCAACATTCCCGGAAATGCGTCGC	TCTGGACCCGAATCACACCCTCAAAC
GCGCAACATTCCCGGGAACGCGTCGC	CACAGACCTCCATACACACGCCCACTTT
GCGCAACATTCCCGGGAACGCGTCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_049137097.1\|1570458_1572891_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213192
NZ_CP013673.1\|WP_007055595.1\|1562374_1564144_+\|aryl-sulfate-sulfotransferase	unknown	unknown	gnl\|CDD\|368677
NZ_CP013673.1\|WP_074710167.1\|1559942_1562240_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007053237.1\|1566569_1567337_-\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP013673.1\|WP_058061085.1\|1553430_1556193_-\|NAD-dependent-DNA-ligase-LigA	unknown	unknown	gnl\|CDD\|236137
NZ_CP013673.1\|WP_007054002.1\|1568409_1569432_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133028
NZ_CP013673.1\|WP_011067936.1\|1550944_1551865_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007053231.1\|1573366_1573732_-\|phage-holin-family-protein	unknown	unknown	gnl\|CDD\|377198
NZ_CP013673.1\|WP_021975473.1\|1565033_1566293_-\|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl\|CDD\|99734
NZ_CP013673.1\|WP_007055592.1\|1564200_1565025_-\|energy-coupling-factor-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213192
NZ_CP013673.1\|WP_007053236.1\|1567582_1568368_+\|nitroreductase	unknown	unknown	gnl\|CDD\|379633
NZ_CP013673.1\|WP_007054010.1\|1552138_1553254_-\|Mrp/NBP35-family-ATP-binding-protein	unknown	unknown	gnl\|CDD\|378455
NZ_CP013673.1\|WP_007053234.1\|1569674_1570328_+\|ECF-transporter-S-component	unknown	unknown	gnl\|CDD\|226129
NZ_CP013673.1\|WP_011067929.1\|1573808_1574459_+\|TM2-domain-containing-protein	unknown	unknown	gnl\|CDD\|377473
NZ_CP013673.1\|WP_007053232.1\|1572962_1573268_+\|YhbY-family-RNA-binding-protein	unknown	unknown	gnl\|CDD\|376702
NZ_CP013673.1\|WP_081040210.1\|1556257_1559812_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP013673.1\|WP_077382781.1\|1575428_1576325_-\|D-2-hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240625
NZ_CP013673.1\|WP_081040211.1\|1574809_1575325_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007054012.1\|1550554_1550767_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380513
NZ_CP013673.1\|WP_007054013.1\|1549601_1550417_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_011067929.1\|1573808_1574459_+\|TM2-domain-containing-protein	gnl\|CDD\|377473	pfam05154, TM2, TM2 domain. This family is composed of a pair of transmembrane alpha helices connected by a short linker. The function of this domain is unknown, however it occurs in a wide range or protein contexts.	8.11009e-15
NZ_CP013673.1\|WP_049137097.1\|1570458_1572891_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213192	cd03225, ABC_cobalt_CbiO_domain1, First domain of the ATP-binding cassette component of cobalt transport system. Domain I of the ABC component of a cobalt transport family found in bacteria, archaea, and eukaryota. The transition metal cobalt is an essential component of many enzymes and must be transported into cells in appropriate amounts when needed. This ABC transport system of the CbiMNQO family is involved in cobalt transport in association with the cobalamin (vitamin B12) biosynthetic pathways. Most of cobalt (Cbi) transport systems possess a separate CbiN component, the cobalt-binding periplasmic protein, and they are encoded by the conserved gene cluster cbiMNQO. Both the CbiM and CbiQ proteins are integral cytoplasmic membrane proteins, and the CbiO protein has the linker peptide and the Walker A and B motifs commonly found in the ATPase components of the ABC-type transport systems.	2.63607e-91
NZ_CP013673.1\|WP_058061085.1\|1553430_1556193_-\|NAD-dependent-DNA-ligase-LigA	gnl\|CDD\|236137	PRK07956, ligA, NAD-dependent DNA ligase LigA; Validated.	0
NZ_CP013673.1\|WP_007053237.1\|1566569_1567337_-\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.26999e-33
NZ_CP013673.1\|WP_007054002.1\|1568409_1569432_-\|glycosyltransferase	gnl\|CDD\|133028	cd04185, GT_2_like_b, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.7976e-76
NZ_CP013673.1\|WP_007055595.1\|1562374_1564144_+\|aryl-sulfate-sulfotransferase	gnl\|CDD\|368677	pfam05935, Arylsulfotrans, Arylsulfotransferase (ASST). This family consists of several bacterial Arylsulfotransferase proteins. Arylsulfotransferase (ASST) transfers a sulfate group from phenolic sulfate esters to a phenolic acceptor substrate.	2.55763e-55
NZ_CP013673.1\|WP_007053231.1\|1573366_1573732_-\|phage-holin-family-protein	gnl\|CDD\|377198	pfam04020, Phage_holin_4_2, Mycobacterial 4 TMS phage holin, superfamily IV. These proteins are predicted transmembrane proteins with probably four transmembrane spans. The 1.E.40 is represented by the mycobacterial 4 phage holin, but it also contains many cyanobacterial. proteobacterial and firmicute proteins. Holins are encoded within the genomes of Gram-positive and Gram-negative bacteria as well as in those of the bacteriophage of these organisms. The primary function of holins appears to be transport of murein hydrolases across the cytoplasmic membrane to the cell wall where these enzymes hydrolyze the cell wall polymer as a prelude to cell lysis. When chromosomally encoded the enzymes are therefore autolysins. Holins may also facilitate leakage of electrolytes and nutrients from the cell cytoplasm, thereby promoting cell death. Some may catalyze export of nucleases.	6.32694e-10
NZ_CP013673.1\|WP_021975473.1\|1565033_1566293_-\|pyridoxal-phosphate-dependent-aminotransferase	gnl\|CDD\|99734	cd00609, AAT_like, Aspartate aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). Pyridoxal phosphate combines with an alpha-amino acid to form a compound called a Schiff base or aldimine intermediate, which depending on the reaction, is the substrate in four kinds of reactions (1) transamination (movement of amino groups), (2) racemization (redistribution of enantiomers), (3) decarboxylation (removing COOH groups), and (4) various side-chain reactions depending on the enzyme involved. Pyridoxal phosphate (PLP) dependent enzymes were previously classified into alpha, beta and gamma classes, based on the chemical characteristics (carbon atom involved) of the reaction they catalyzed. The availability of several structures allowed a comprehensive analysis of the evolutionary classification of PLP dependent enzymes, and it was found that the functional classification did not always agree with the evolutionary history of these enzymes. The major groups in this CD corresponds to Aspartate aminotransferase a, b and c, Tyrosine, Alanine, Aromatic-amino-acid, Glutamine phenylpyruvate, 1-Aminocyclopropane-1-carboxylate synthase, Histidinol-phosphate, gene products of malY and cobC, Valine-pyruvate aminotransferase and Rhizopine catabolism regulatory protein.	2.80797e-50
NZ_CP013673.1\|WP_007055592.1\|1564200_1565025_-\|energy-coupling-factor-ABC-transporter-ATP-binding-protein	gnl\|CDD\|213192	cd03225, ABC_cobalt_CbiO_domain1, First domain of the ATP-binding cassette component of cobalt transport system. Domain I of the ABC component of a cobalt transport family found in bacteria, archaea, and eukaryota. The transition metal cobalt is an essential component of many enzymes and must be transported into cells in appropriate amounts when needed. This ABC transport system of the CbiMNQO family is involved in cobalt transport in association with the cobalamin (vitamin B12) biosynthetic pathways. Most of cobalt (Cbi) transport systems possess a separate CbiN component, the cobalt-binding periplasmic protein, and they are encoded by the conserved gene cluster cbiMNQO. Both the CbiM and CbiQ proteins are integral cytoplasmic membrane proteins, and the CbiO protein has the linker peptide and the Walker A and B motifs commonly found in the ATPase components of the ABC-type transport systems.	9.33527e-28
NZ_CP013673.1\|WP_007053236.1\|1567582_1568368_+\|nitroreductase	gnl\|CDD\|379633	pfam14512, TM1586_NiRdase, Putative TM nitroreductase. Compared with the more traditional NADH oxidase/flavin reductase family, this family is a duplication, consisting of two similar domains arranged as the subunits of the dimeric NADH oxidase/flavin reductase with one conserved active site.	1.08023e-56
NZ_CP013673.1\|WP_007054010.1\|1552138_1553254_-\|Mrp/NBP35-family-ATP-binding-protein	gnl\|CDD\|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	1.59874e-97
NZ_CP013673.1\|WP_007053234.1\|1569674_1570328_+\|ECF-transporter-S-component	gnl\|CDD\|226129	COG3601, COG3601, Predicted membrane protein [Function unknown].	3.41572e-18
NZ_CP013673.1\|WP_007053232.1\|1572962_1573268_+\|YhbY-family-RNA-binding-protein	gnl\|CDD\|376702	pfam01985, CRS1_YhbY, CRS1 / YhbY (CRM) domain. Escherichia coli YhbY is associated with pre-50S ribosomal subunits, which implies a function in ribosome assembly. GFP fused to a single-domain CRM protein from maize localizes to the nucleolus, suggesting that an analogous activity may have been retained in plants. A CRM domain containing protein in plant chloroplasts has been shown to function in group I and II intron splicing. In vitro experiments with an isolated maize CRM domain have shown it to have RNA binding activity. These and other results suggest that the CRM domain evolved in the context of ribosome function prior to the divergence of Archaea and Bacteria, that this function has been maintained in extant prokaryotes, and that the domain was recruited to serve as an RNA binding module during the evolution of plant genomes. YhbY has a fold similar to that of the C-terminal domain of translation initiation factor 3 (IF3C), which binds to 16S rRNA in the 30S ribosome.	1.56123e-31
NZ_CP013673.1\|WP_081040210.1\|1556257_1559812_-\|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.	2.2362e-07
NZ_CP013673.1\|WP_077382781.1\|1575428_1576325_-\|D-2-hydroxyacid-dehydrogenase	gnl\|CDD\|240625	cd05300, 2-Hacid_dh_1, Putative D-isomer specific 2-hydroxyacid dehydrogenase. 2-Hydroxyacid dehydrogenases catalyze the conversion of a wide variety of D-2-hydroxy acids to their corresponding keto acids. The general mechanism is (R)-lactate + acceptor to pyruvate + reduced acceptor. Formate/glycerate and related dehydrogenases of the D-specific 2-hydroxyacid dehydrogenase superfamily include groups such as formate dehydrogenase, glycerate dehydrogenase, L-alanine dehydrogenase, and S-adenosylhomocysteine hydrolase. Despite often low sequence identity, 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. Some related proteins have similar structural subdomains but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence. While many members of this family are dimeric, alanine DH is hexameric and phosphoglycerate DH is tetrameric. Formate dehydrogenase (FDH) catalyzes the NAD+-dependent oxidation of formate ion to carbon dioxide with the concomitant reduction of NAD+ to NADH. FDHs of this family contain no metal ions or prosthetic groups. Catalysis occurs though direct transfer of the hydride ion to NAD+ without the stages of acid-base catalysis typically found in related dehydrogenases. FDHs are found in all methylotrophic microorganisms in energy production and in the stress responses of plants.	1.26253e-119
NZ_CP013673.1\|WP_007054012.1\|1550554_1550767_+\|hypothetical-protein	gnl\|CDD\|380513	cd06290, PBP1_LacI-like, ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. This group includes the ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	1.16807e-07
NZ_CP013673.1\|WP_007054013.1\|1549601_1550417_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.0086e-69

>NZ_CP013673.1|WP_021975473.1|1565033_1566293_-|pyridoxal-phosphate-dependent-aminotransferase
MHFSSRVDISAPNPIAAAEAAAKANGIALSKLNDSNPTRHGLAPELVPSVYTADPRGPRAAREALAAFLNTAKAVDASSPQSTSPAASEGGNERHAAFNNANTAIEGVDPDALYLLSSTSEAYSWLIKLLCDAGDAVLAPKPGYPLIESIARLECVDTVEYQLQFDGSWFIDIAELERLLSEPGGERIRALVLINPNNPTGSYVKPTERARIVTLCREHGIALIADEVFFDYSLEPFPGNARLAGERGVLTFALDGFSKMLAAPHAKVGWIQVSGPAEDVAEAQRRLDVIADDYLPMSDIIAERIPALLNAAPAQTRRVGERVRNNLAKLHELLDADPNGLVSVLRAEGGWNVLLRVPSVIDENELVLRLIDEHKLTGQPGYFFDMTSNGYLAVSLLPEPDEFERGIRAVLNTVAALLR
>NZ_CP013673.1|WP_007055592.1|1564200_1565025_-|energy-coupling-factor-ABC-transporter-ATP-binding-protein
MPAPRLYSTYNSGMGFLFRPKELPRPASLTFTLDQAGHTYDDGHVGLAPTDITISELRVAVIGLNGAGKSTLLGLLDGSLKANAGTVTIAGGEERLDPAVKKDAKRIDNLVGKVRREEIPNSFYQAANISEAVSEALKKHKVPESERHARIGNLFAHFDLAQVSKAKASELDSEKRHLLAIAAALSFEPSAIVADEPSKGLDEIGAAHVAKALFSYNKQVIFATHDTDMIRRPEYAIDRVLVLDEHAVAFDGAPAEAVAFYEDLIRRKYEAAKR
>NZ_CP013673.1|WP_007055595.1|1562374_1564144_+|aryl-sulfate-sulfotransferase
MSTAVRSRVFKISAAAVTAAIAIGLCLFSQDDVSASIKERRVERLNAQIENVYTDEYQQMMDTEIADERDAKERTVDSIYTKVNPYGTNTTSMYVYFTTDQASTVSYTVSAEGYPDYTANAITSDEAAAAYREAAAGDADGSGNVGGTSTASQTTTVSSNDIASTEHEFLVLGLIPKVKNTITLTITDTDGNATTRTIEQTGPKLLGEEEVRLEQAVAPDESTVTTLGNGLYAILGNDSNEQDFMYYYDANGVIRGEIPVLYYRSHRLLFDNDGIMWFSASTKHFVGMNRLGKLVKIINLGDQYILHHDYALDSDGNIVSLATDLKHSDHAVQDQVIKVDTDSGEVSLLVDFGDLFPDYKQSTDHSGIDESDPTATNRWDWIHFNTIQLMDDGSALLSARETSTMIKINDIEGTPSLDYMIGEPSVWNGMDAQPSFLTKVGDSGDTGGQHSITVQYDSSLEDGQYYIYMFDNDFGYAMTRPDFDWTMIDGISTAQSSKDENSNSQFRKYLVDENAGTYTEVQDFDVPYSPYVSSAQELSDDLNLVDIGMQGLFGVYDDDGNLKAQYKMVLSSGYIYRVYQYGFRGFYFA
>NZ_CP013673.1|WP_074710167.1|1559942_1562240_+|hypothetical-protein
MHSIDHTRADRPMPSNHERHLPSRPDTRHRLRLVRLLIALLAAVAAIAAMECIVFNLPFWRTLGASTDTNAVHNTLGSGLTRRNDGMLTVTDPTKAYLELTADGTSDYLRIDTESSKVIDKAREQAEAESKANDDKEVFKPLATIHVRADVDGITGKAQSMNPDAIRSHYVKAPGAGIVRIWIQEERGAIVPVTDARANVRVPFVINWMRVLAMALVLLMIAVWRPGSRLWRITLDPSSTRQRLAFVGLLAIPTLLIGVSIIHELWYTSSLVFHVSGDYTYDFDQYGHVADALVAGRPWLDLPVPEQLAATEHPYDVATRAQLLANGASPLYWDYAYYDGHWYSYFGVLPAVLLFVPYRLLAGHNLPTSAAEYILVLLFIIFFSLLVLRVIHRVMPKTSVAAASLVVVSSLVSAQMGYLLYRTNFYQIPFAASLTLTSLGLWLWLGADTSRRPLRPSDRWQAGDAKPLSLPRLALGALCIAANFGCRPTFTLAALLAFPLFWPQIRALGTGLRTRRIKPLQALRAPLAVIIPAILVVTPLMAWNMVRFDSPFNFGNAYQFSISDMTRYTTPSADMPANIWYYLFLPLRFMDRFPWLAGSPAPMPQWGYYEVMVGAIFTATPLTLMALALPLLRRLETHGMRPWLMSCLAVAAVLVVFDSRVGGLGWRYSADFGWLISLASIPGLLWLVNGREPSRSLAGANDAASGDGIARVTPWRWLMRWVVMLAVLWALGIAILSCFVQSRSDSMIANNPTLWHQVQSWFTLL
>NZ_CP013673.1|WP_081040210.1|1556257_1559812_-|tetratricopeptide-repeat-protein
MNALAADLGLSKPKKHDTNPFGDALREISERKGGIIDELTRHAVALSPVIKRRTFPELENVPEGLVLGWAQLPSTRGRGFSLGIFPDRDHFAQVAFADTHGRVFVGTDPNMDVQDMQARFMFGKEKEVTLPDGERLGESDEPRSRSGFSRTGHGLGSALHHGRGLGRGLGHGADGVKAITGGVVGRDDTGRMTWLASWLKAGNRYTLEQMRANLPPVMRHDLEYRDAITIAFFATYMLPQINGLLIGFGSGNIFRRLNREAPIGAIRRSVRDTLAARAHGMRASGLEDHFANLMREAGALDTTPGLEAVHGAEPLHLYTSTYSSGYFFTWDKSLAFGQALKSLKIEGNLNRFAAVSAWLERNASLGRNPTEDTVTRAEAAQIDMKLIENPAIMALDPYDGEQERRAVLSLVDIAARTAGQIRSEFPDPRDVLTQQNVPDSGVTNAAGAESTESVEGAVERTNKSDTNTQAARPSCSPARSDEWVYRQTLSSLLRRLRLPYRFDVEFRSRLDSGEVAIGFTTAGTSMMPDSRYDTTRRTWRALSSAERASMSAAYNLRVGLMMAALSFGTSESVRQVSLHIDSIGLEEAIAEQDSAIEAMMSEALSAFEHLRSGDLGRVGSKADPKDGDFHGDPTRPITHEETFGQTASGDERGTAGGAGNGTGPSADATDQAAAESADADGAASIDSQFEDLMKGIDIDEMAFGMPDDTGAGDDLGGIGGEGVGTDGADGAAGMDDDPMSVLRRNPTVRNMVTVTFTRDAFLKRLDTAGLDNPEETYRMFGAVMDVDGEGGLKPISADFDLADSRFSPTGSQEEPELADRQFSPATAHVLGAQNSAGLAIQRVDLLQHGVNEFHDIARNTSLGSVEKAQRAMQVIESICDPELTGLASQVTSALIDGKDTPDFTFTLADDLDKERLRARDMLFSGQADQAIEAAEAAVAHLDQVYAAGHGVPRYFNSYAERVVYNRLFATLDERTVLIPDNLFYAHMELADVLSQIKGAEAAIPHLNRMVAYAPAYPLSHLKLAIQLARNEDWDSARAACLNALRVALDRDDAAFAYYRFAYAEWMLDRFDTAAAAYIMSDHIAPGAIGSLESELQELVSRADSQCIPVPESVEAAAHVLATHDLPVWPHIEVADIVRDAARVCVDEDMFVPARTLSVAVARMNDGEGDNIDIIQAQFLRSLSA
>NZ_CP013673.1|WP_058061085.1|1553430_1556193_-|NAD-dependent-DNA-ligase-LigA
MSTNEQLAWDFDDGDVAEVRPDTGIARFAPGSEQWIAALQPTDDDAIRLDRFDVNTMTAEAAARLWARVAAWVESDQIAYYIDDSPVSSDAAYDARMRCLERLEAAFPSLDNPQSPTHRVGGSFSNDFASVRHPSRMMSLDDVFSIEELKDWYDSVIRDLDWPESKPLPMSCEVKIDGLALNLIYRNGVLEQGLTRGDGVTGEDITLNVRTIGSIPANLGGPKEDVPDFVEIRGEVFMRWDDFHTLNNEQEDAGRAPFANPRNAAAGSLRQKDPRITATRRLSFYAHGLGQLTWGPDHPRGTHDVVADQSQAYDLYTKWGVPVSPHNRAVTSFQEILDMIEYYGEHRGDIEHALDGIVVKVDDLGLQRTLGATSRAPRWAIAYKYPPEEVNTELLNITVQVGRTGRVTPVAVLKPVYVAGSTVARTTLHNGFEVKRKGILIGDTVVVRKAGDVIPELVGPVLERRKGREDQLREFVMPEFCPSCGAKLSPAKEGDKDIRCPNVESCPAQLTERVISLASRKAFDIEHLGEQSAIALTNPEENRPDSVATYAPNITEVLVAPGEEPDPYEPVEGLELPVAQKPVLSNESGLFNLTAADLRDVRVWREAAIVEVHETVGANGKKKKVRKRVGGSGLWHQVPAFWTAPTPAKKLTAKQLAERAQGEAAIESAETQGGTASETTGAPTGAEAPLGTMPGFAAASYPEYDVPADAVIVRVDHKTTRTGVTDVPVIIRPGENTRKMFDEMDKARHADLWRVLVALSIRRLGPPTARLIASAMGSLAAIENATIEDLTAIDGVGPEIAESVVNWFAATREPGDWRGATLRAWQAAGVGVDEAETSSLPQTLAGKTVVVTGSLEGYSRDSAKEAIIERGGKAAGSVSKKTDYVVIGANAGSKAAKAEELGIPMLSETQFAQLLATGTI
>NZ_CP013673.1|WP_007054010.1|1552138_1553254_-|Mrp/NBP35-family-ATP-binding-protein
MSDARQIEADIYERLSKVIDPELGRSVTDLGMIAAIEAAPASSDAGTYDVTVHVELTVPGCPLSETITSQINGAVSSYPGAQLLPHIEVGSMSRDKLADLVADLKAERKQNPFSKPGVKTRIFAIASGKGGVGKSSVTANLAATFAALGFDTAAIDADIYGFSLPRLFGVHTQPTNLNGMLMPVTAWGVKLISIGMFAGADRAILWRGPRLQRSLEQFLSDVWWGEPDVLLLDLAPGTGDMAISVAQALPNAELVVVTTPQPSASDIAVRSGLVALQVPMKVRGVVENMSYYEHKGEKLEIFGAGGGQRVSEQLTQALGYDVPLMAQLPLEPEVRETGEAGRPAVLDADGALRTDGIGQTFRGLAERLLAV
>NZ_CP013673.1|WP_011067936.1|1550944_1551865_+|hypothetical-protein
MDNSISWNHIALPGLHSSPNQLYGRTMSSFMHEDIVGRRRAERERCNDAARRSKGPLLVGYINAANYYGAPIPRHCTLSVDAVHACVSSANKRRRIKGVVFHVFKGKLDIRKKDYEQFWIASPVMMWAQMAQYSTLEELAAIGASLMSRDKRRRMATRKDFDTYLEISPRFIGRNKCHEALPYMTENTDSPPENTLFGMLKDSGLGCPTANYRVNIGNSYVILDMAYPDCRVAFEYQGAYHADPAQMRIDAAKRNALQLLGWIVILVTADDLRTADTRHRFIEMAHVVVSRQRNLADWNRSWAITS
>NZ_CP013673.1|WP_007054012.1|1550554_1550767_+|hypothetical-protein
MLGRGYRRIAYIIGPSYLPTSTPTPACPQLTTVRQPMDAFGVSLATLVLDQIEDRPFQRTGLLPTEVVAR
>NZ_CP013673.1|WP_007054013.1|1549601_1550417_-|carbohydrate-ABC-transporter-permease
MKCVENPRAVSHGAAQSAPPRRRTNPGKIARRAGTTILALLFCVVWFFPVYWMIITAVKPRDEIMTTTPVFWPMHLSIVLSIIVAFFACTALTLYRFRGRKPIMVFVLAIQMTSGGIIPQIIIYNQLGLLNKYSGLILAYIAMVLPFAIWNMRGFFLNIPKDIFESAAVEGANDWQILWKITFPLAAPGIVSTSVFAFINAWNDYMIAYTFMKDQSKYTLPVWLSSFSTPTMGTDFGGQMAASVTFSLPVVVFFMLIQRNIMKGVTTGAVK
>NZ_CP013673.1|WP_007053237.1|1566569_1567337_-|ROK-family-protein
MIETAQAFGVDIGGSGIKAAPVDLTKGDFAEPRLKILTPEVSTPQAVAKIVKQQLDHFEVPESAPVGIAFPAPIKPGQKLDFMANLDQSWIGVDVTEVFSEACGRPVVVVNDADAAGLAEVQFGAAKGQDGLVIATTLGTGIGTALIYNGVLIPNTELGHIILSAKHLDAEKYASSAIRENEELGYKKWAKRLTKYYGLMEKYFNPDLFTVGGGVSRQSEKFLPYVDIKTPIVPAKLRNQAGIVGAAYYASTKQQ
>NZ_CP013673.1|WP_007053236.1|1567582_1568368_+|nitroreductase
MAEHTQLIDAINIRTAVRAYDDEPIDDDTARQLEMALQPINLLGDLNIQLVRDQPKVFAEANASGHLTNAANYLAIVGPANDEEAKERAGFYAERMVLTATLRGLGTLWVAGSWDKAEAAKHCRVTSGQELYLGVVIGHPKNHLDYQAKSYEELCEAQRTHRATKTYEQFTATMSDEGREAAPDWFKSGVEAAMKAPSAMNRQPITFSYNPADDTAAAHIDQSAEDEHHAFNDMGIAKLHFQIGAGQGQWAWGDGGLFIHK
>NZ_CP013673.1|WP_007054002.1|1568409_1569432_-|glycosyltransferase
MGAMAEVKKPNNTIDKLALIVTTYKRQQLLETLFDSILALEQAPWRIVIVDNEQSDQTADMVAAFAGKVTGQWGTTVADQSGNEERVVYAPQTENLGGAGGFSAGVAKAYELGAAWFWVMDDDVAVLPDAIAKLSKWTDKHEVIQGSRFDYDGGPFYWQYDFIVPLGIPNPIAPAAFGPAGYRVMDTLCFEGGLFNRRVVTEIGLPDPRFFIYWDDTMYGYRASKVTNPIVVPDVILRRTREIGNWDIAGVRQLNSTSDMNRYHIMRNRGYMARYFMTYGDFRPLVFGLGTVLTAAKEVIRLVMVDREHLKTGLVQIAKGWWDSRKLMHDPTWKPMPSLK
>NZ_CP013673.1|WP_007053234.1|1569674_1570328_+|ECF-transporter-S-component
MSVSSRIRMQVVRSVAPEAEGSASTSTASTSAKLGSHTTGVADSGRWSTRRIAMYALFVALAMVTSFIEFPITPVTWLKYDPSGIVCLIAGFAYGPAAAAIVSVLGFVPHMFANPWGSLMAVLVALFLSVPAAFIYRKIRTRKGAAIGILVGAVLAIVVALVSNLIVTPIYAHMTYQAVAAMILPILLPFNVAKMAIHAVITFLIYKPISNLLSKQQ
>NZ_CP013673.1|WP_049137097.1|1570458_1572891_+|ATP-binding-cassette-domain-containing-protein
MTVAPHSFDADEFHDSAEPHASAEPASPAAVLKDIRFSYDRGTSWALDGVSLTVHAGERLCLVGPNGSGKSTLARLIAGLTAPDGGEVTLLGQRVYAAGPNADAYRAARHGIGMVFQNPEDQLVTTVLEDDVAFGPENLGLERELIGERIVDSLQAVGLANLRQSDPTRMSGGQQQRASIAGMLAMNPAMLVLDEPTAMLDESARAEVMRILDDLQARGTTIVHVTHHPDETVHADRIVHMEAGRIIGITAAVDNRSPLAEAVSQSETEGSIGTEAAPSRPTNDSPRQREREDGSELPLLSDGIGDMTNPIIRVSHLTYRYPSAKRAVIDDLSFTIARGETVALMGVNGSGKSTLVRMLCALTAPTAGSIEVAGVPVASTGKRGRNVRPKSANRKQLAQLRRHVGYVMQHPEHQLFADTVAEDVAYGPRNQGLGETEVADRVRESLELLHIGHLADRSPFDLSGGQQRLAAIAGMLACNPDVLIMDEPTASLDAQAKKRIHELLRTLKSRGVTVLIITHDREEAEQIADRVVRMPIAAPASGGPVTATVTEPAVSSNGPAHSVIHRLDPRVKMVGFLAAMFTMFAVNTPTQLALGIAITLAVIAAARLNPLRVLESIHPILILLVLMGVVNLFVVRTGTPVVALGPLSITDQGVTIAVLYACRFALVIILGAVFLTTTTPTAMTDAFATLISPLNRLGIHAQEIALVMSLALRFIPTLTDETRAIVDAQSARGGSIETGSLAQRIKAMSAIIVPIFAGTLRHADNLSLALDARCYEEGIRRTHWRALTIAARDLIFAAAVIIYIAAIIAL
>NZ_CP013673.1|WP_007053232.1|1572962_1573268_+|YhbY-family-RNA-binding-protein
MALTKKQIKQLRAMANSLKPLFYVGKNDLTESAVNQADETIEKHELIKCAVQDGSGLTAKEAAAELAEQLNAEVVQSIGNRFVLFRRSRRDDVEHIRLVRE
>NZ_CP013673.1|WP_007053231.1|1573366_1573732_-|phage-holin-family-protein
MRSFLTSWLIMTIAAAVMVAVTPGMTPVGEPPILGIAAFALFMALINASIKPIVHLIALPFAILSLGLVTLIINWLFMRLASWLAVSLFGVGVFVHGFWWSVLGSLVLTIVAGIVGSILDQ
>NZ_CP013673.1|WP_011067929.1|1573808_1574459_+|TM2-domain-containing-protein
MPFPIERGLTRMTDNQQQPYGSDSVPQPAQPAQPAQPSYGQDAAQQPQGYGAPQPAAYAQPAAGSYGQQQPQYGQPAGAYAQPQYGQPQYGQPAQPAAGYGQQPGYGQAYQQPNAYAQPQYTAAPYAAAPVGQSSKSKLAAGLLGIFLGGLGVHNFYLGNTGKAVAQLLLTLVGWILLGLGPIAAAIWGFVEGIIILCSKPGSPWHKDANGYELSD
>NZ_CP013673.1|WP_081040211.1|1574809_1575325_-|hypothetical-protein
MVDSQYQSVLVRADTLELHVEATLVMQEHAGAIAVDRTVREQHTNGECGLHVLRQRQECLVGVPVRVVHHGGTGHVGVTVAILVDVSHERQIPGVVFGELCLEVLDLGQRRVAQAEALGHFIGLGCFRIRVLAEHIRVDNDDFSLRHNVFLSAWRSPSKHLGKYWHCSIHI
>NZ_CP013673.1|WP_077382781.1|1575428_1576325_-|D-2-hydroxyacid-dehydrogenase
MPQEFVGDEAHRGDMVWSAAVPEELRSRATAVIGNFPVSQASQYTRLEWLQTFSAGVDAYICPGVLPRGTMVTNASGAYGQSVSEHMFATMWALMKNLNRYASNQRDHQWQDEGPVLSPEGGIALIIGVGDIGSHFAQLAQSVGMRTFGVRRHADVPAKGIEKMYGFERLETLLPLADVVAMAVPRSPQTHHLLNADRLGRLKSTAIVINAGRGDAIDPEALADALHNGRLHGAGLDVTEPEPLPAESPLWDEPHCLITPHVAGGNHLEKTSEHIIRIALTNVSRYAKQQELLNLVRY

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Crispr_ID: NZ_CP013673_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_5

1656102-1666931

TypeI

I-C

Consensus_repeat	Method
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	PILER-CR
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CRISPRCasFinder
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CRT

163 spacers

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

The CRISPR arrays of NZ_CP013673_5

>merge|NZ_CP013673|5|1656102-1666931|PILER-CR,CRISPRCasFinder,CRT
ATTTCAATCCACGCACCCCAGTGGGGTGCGACGCCACGATTCCAAGGATCGTGTCGACCGCTTCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACATGCGTATCCTGCTCTGCCACGCAAAGTGCAGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACACGAGTGTGAGCGCATACGCCTATGATGCAAGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACCTAGATAATCGTCTAGGCTGATGTCTTGCGGCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACAGCGCGGTCATGGTTTCCTCCTTAAAGGATCGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACACCTGCAACTGTCTCACTTGACGTACCGTTTTGAGATTTCAATCCACGCACCCCAGTGGGGTGCGACCAACACGCGACTATCAGCCTTGCCATGCTTAGGGCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGTTCGTCAGATACACCGTATCCGCGTACCCGTTATTATTTCAATCCACGCACCCCAGTGGGGTGCGACCGTAACGGGTGGTGCCCCCGCAGTCCTCAACCTCATTTCAATCCACGCACCCCAGTGGGGTGCGACTCCCTTCTGATTATCAGTCTTCGTACAGGTCATCATTTCAATCCACGCACCCCAGTGGGGTGCGACGAGATTATTCACGCCGTTGGCGGGTTCGATACGATTTCAATCCACGCACCCCAGTGGGGTGCGACCGACGGCACGGCCACGTTCCGGTCGGACGCGGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACTACAGATAACCAGTTAATCAGCGACACTATGATAGGCATTTCAATCCACGCACCCCAGTGGGGTGCGACTGACCCGAACAGTGGCACGGTACAGCAGGTGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACCATGCCCAGGAGGATTCGGCCGAGCGAACGGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACCGAAACCGTCCTGCAGGCGGGTCGATTGTCCGCAATTTCAATCCACGCACCCCAGTGGGGTGCGACTTCCCCACCACGTCCGCCGTGGGGCGCGTTTTCGAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCCGCGACGCCCGATCGGCGGACTCCCACGAGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACAAACGAGGCACAGGAGCCGCAAGGGAACGAGCCCATTTCAATCCACGCACCCCAGTGGGGTGCGACATCTTCTGGTTCGCGCCGTCGCGTCCGCCAAATGAATTTCAATCCACGCACCCCAGTGGGGTGCGACACAAGCGACACGCTCTATTTTTGTTACAGAGATATTTCAATCCACGCACCCCAGTGGGGTGCGACGGCGACACCATCATGGACGCCATCATCCCGACCATATTTCAATCCACGCACCCCAGTGGGGTGCGACGGCGCGCGTGGTTTAGGTAAGACATACGGTATACATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGGCTTCACCGATTCAATGAAGGCCAACGTGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACTGACCGGTCTTGCCGTTTACCTGACCGTCCAAGGGATTTCAATCCACGCACCCCAGTAGGGTGCGACCACCACCTTGGCGGTAGACCCCGCGCCCGTCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACTTAATTACCGTGTTTGGCGTCCAAACATTGTAATCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGCCGGTTACTTTTTGTAACCGAGTGTGGTATGATATTTCAATCCACGCACCCCAGTGGGGTGCGACCGCAACGCCTCTGGGAACGAGCCCTAATAGCCTATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCGTCGGCTGCCACCTCGCGGTTGTCCACGGGGATATTTCAATCCACGCACCCCAGTGGGGTGCGACGCAACATCACCACCATCTGGGTGCCGGCGATCAAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCAAAAATCTCACAGCATTAGGCGTAACCGACACCATTTCAATCCACGCACCCCAGTGGGGTGCGACAAACCTATGGTCGATCAGATTACAGAGATGTATGAATTTCAATCCACGCACCCCAGTGGGGTGCGACCAGGAGGTCAGGGCTCAAACGCTCAAGCTACTTCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGCCTTGTGTTTCCACCCGTCCGGCGCGATGGATTTCAATCCACGCACCCCAGTGGGGTGCGACGCTGATTCCACGTGTCCGGCGTGCCGAAAATGGCATTTCAACCCACGCACCCCAGTGGGGTGCGACGGTGCTTGGGACTTCACGATTCCCGTGGGTGTCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACACGATCCCGCGTGGCGATGCCGGGACTGCTGGCGTATTTCAATCCACGCACCCCAGTGGGGTGCGACTATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAGATTTCAATCCACGCACCCCAGTGGGGTGCGACTATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAGATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGGGCGATTCTTTCTTTTTTAGTTGTTCAAGAGATTTCAATCCACGCACCCCAGTGGGGTGCGACCTTGCCTCTCCGACCACGCGCGGGTCAAACATCGAATTTCAATCCACGCACCCCAGTGGGGTGCGACTCAAGCCGCAGCGGATAGTGCGAGCAAGGCCGGGATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCTACGTTGTCCATCTGAGTTACCAACTGAGCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTGCCGCAGTATTGGCATGGTTCGGTGGTGATATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGTCTTGCTCATTTGAATACTCCTTCGCAGTGATTTCAATCCACGCACCCCAGTGGGGTGCGACGAGGCCACGTCCTTGGCGAGGTCCTTGCCCTGGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGGCGGAAGCTCAGGTTGTTGAACATGCAGTCCGAATTTCAATCCACGCACCCCAGTGGGGTGCGACGCGCTGATGATTGGGCCGATCTGCTCGCGGAAGATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGCGTTGCTGATGCCCCACAATTGGCCGTTCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACTTCACGCGCCGTGTTCATTTGCAAGACGATGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACTTCGGGCACGATCTGGCAGTCGCAGTCGTCGTGATTTCAATCCACGCACCCCAGTGGGGTGCGACGGCCATGTCACGCCAGGCACTGCAGCGCATGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGGCAGCAACCGACGCCTTGCCTACCTTGTCCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACGATGCCCTGGCCGTCGATCTTGCCGACGACGGCATTTCAATCCACGCACCCCAGTGGGGTGCGACTTGACGCGGGTGATGGCACGGGTCACGTCCTGGTCATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCATGGCTTTCCAAGATCGTTGTAGCCTTCATCAATTTCAATCCACGCACCCCAGTGGGGTGCGACACGTAGGGAAACACGTTGTCGTAGGTGTCGTGATTTCAATCCACGCACCCCAGTGGGGTGCGACCACGCAAGGGCTGTTGATGGCGTCGCCCGCCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACAAACCGTTCTGGTTCAGTTCTATGACCTTCTTGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACCATCAGGCCCAAAACCGTGGCCACGCCGCCACAGATATTTCAATCCACGCACCCCAGTGGGGTGCGACCTCAATGTCACGGCACCATGTACCGGGCAGGGATTTCAATCCACGCACCCCAGTGGGGTGCGACGATATCACCGCCACGCTGTTCGGCGTGTCCGGCAAATTTCAATCCACGCACCCCAGTGGGGTGCGACTCTGCGGCCGGTTCTCCACACGGTTCACGGTCGTATTTCAATCCACGCACCCCAGTGGGGTGCGACCGCCACTCAACCCATTACAGTCTTGTGTGCCAGAATTTCAATCCACGCACCCCAGTGGGGTGCGACCTGGAGTTAATGCTGAGCGTGGGTAGCATCGTGGCATTTCAATCCACGCACCCCAGTGGGGTGCGACGTGCTTGGGACTTTACGATTCCCGTGGGTGTCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACTCACGGTGCCGTCCAGGCCTCTCAATTTCAGCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCTGGTAGGCGCTGTAACGGGTGTTCGTGTCGATTTCAATCCACGCACCCCAGTGGGGTGCGACTCCAGCAACATCAAGGGATATGTGACCACCGAGCAATTTCAATCCACGCACCCCAGTGGGGTGCGACTTGTTGTCCTTGGCGCGTTTCTCCCATTCGCGGGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACAAGGCTGGACGTGACGACGGACGCGACCTTGCTATTTCAATCCACGCACCCCAGTGGGGTGCGACAATTACCTTGAGTGAATCGGCCGCGAACTTTGAATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCATGGCTTTCCAAGATTGTTGTGGCCTTCATCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCACTCGTCCAGCAGCCGAGGGCTTCGTGGCGTATTTCAATCCACGCACCCCAGTGGGGTGCGACCAACACACCCTTCTCAGGTGCCATCACACTATCGATTTCAATCCACGCACCCCAGTGGGGTGCGACTGGTGGGGCCGGTAAGTATCACGTCGGTATTCCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCAGCAAGAAGGAAGAGTAACCCATGACCAGCAACATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGTCTGGCTGCCGCCCTCGCTGTGCCCGTCAAGATTTCAATCCACGCACCCCAGTGGGGTGCGACGAACGCGCGCCGCCAGCCGGCCGGGTCGTCCGCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGTTCGACCGACTGTGCAACGCATTGCGAGTGGCCATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTGATGGCTATCACTATACGCGGTCCAATACTGATTTCAATCCACGCACCCCAGTGGGGTGCGACGACGCCTGTACCTCTCGACCGATTGGGGAGTAGAATTTCAATCCACGCACCCCAGTGGGGTGCGACTCGGTGGTCTTCGACGAGGAGGTCATACCAGTAGATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGTGTTGGCCTGCACGGTGCTCATCTGCTGGTCATTTCAATCCACGCACCCCAGTGGGGTGCGACGCCGCCTGAGTAGGGCGCGCCGTTCTGGATAACTATTTCAATCCACGCACCCCAGTGGGGTGCGACTTGGGCATCCCGGCGTCGTTGATGCTCGCGAAGGTGATTTCAATCCACGCACCCCAGTGGGGTGCGACTGGCCGCCCTACGCGAAGAACTTATCGGGCTTATCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGTGACATCCAGTAAACACTGCCACTGGATCGCATTTCAATCCACGCACCCCAGTGGGGTGCGACCCAGCCCGGTTATCACACCGGGCTGGTTCATCTATTTCAATCCACGCACCCCAGTGGGGTGCGACTTGTTGGCTCCATCATAGGTATTCCCAATTGGATTTCAATCCACGCACCCCAGTGGGGTGCGACTAACCCACGTCGCTTACTGGAGGCTCCAAGCGAGTCATTTCAATCCACGCACCCCAGTGGGGTGCGACGACTTCGCGGTATCACTACCGCAAGCGGACAGGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACACCGGCCTTGTTCGGGTTGCCGGGGGTGATCTGATTTCAATCCACGCACCCCAGTGGGGTGCGACCATCACGTCGGAGATGGTCTGCTGGTCGGCGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACGCACACCGCCGCTCAACCGTTCGCACTCCGCCATATTTCAATCCACGCACCCCAGTGGGGTGCGACACACCACATGCCCCGACCTCGCGCCGAACGGGCTATTTCAATCCACGCACCCCAGTGGGGTGCGACGATTCTTGGCGGCTTACTACAGCAATCAGGTATAAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCCCTCACATACGCTTCCTGCATCTGCCAAAACGTATTTCAATCCACGCACCCCAGTGGGGTGCGACAACACCTCATTAGTCACCTGCGTTTTCTGTTGGATATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTTGCGCTCCCCCGTCGCGGTCTGTTTCACGTATTTCAATCCACGCACCCCAGTGGGGTGCGACTCATAAGCCGGTCTTCTTCGCGCAGCTCACGCGAATTTCAATCCACGCACCCCAGTGGGGTGCGACAGAGTATCGAGGGCGTGGACGTGTGTTGGGTGGAGATTTCAATCCACGCACCCCAGTGGGGTGCGACGACAGGTCAACAACAACTGCCTCGTGTCCGGCGTATTTCAATCCACGCACCCCAGTGGGGTGCGACTATACCACGATGCGGCAACAGCCTACTGCCGGTTGATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTGCGCTGGTCAAAACGGTTCACCTCCTCGACGCGATTTCAATCCACGCACCCCAGTGGGGTGCGACCCAGCTTCTGGTTCCCCGTCGGCTTGGCGGACGATTTCAATCCACGCACCCCAGTGGGGTGCGACATCGCGTCTCTCAAGGAGGCCCAAAGCATCTGGATTTCAATCCACGCACCCCAGTGGGGTGCGACTTCCGGGGCTCCGGCTTCGGCGAGGTGCGTGGAATTTCAATCCACGCACCCCAGTGGGGTGCGACAACTTACTTAATTGAGCTATAATTATTATGTCAACATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGGTGTGGCTTGGGTAGGCGTTCCACGCCGTGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACAGCATGTCGGTGTGCGGCTGCATGGTCATCTGCGTATTTCAATCCACGCACCCCAGTGGGGTGCGACGCGCGCCACCCGGAACTCACGACAGTCGTTACTGATTTCAATCCACGCACCCCAGTGGGGTGCGACTGACGGCGATCAGCTTTGTCTTCTGGCTCCCTGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACGATTGTCTCGTTGACGGATGTGTTGCTGACCTGAGTATTTCAATCCACGCACCCCAGTGGGGTGCGACGCCCGCTTGACGTGCGCTCAATTGAGCGCAACAATATTTCAATCCACGCACCCCAGTGGGGTGCGACGAGGAATCACCGATGCAACCATCACCCTCATCCCATTTCAATCCACGCACCCCAGTGGGGTGCGACATGAACAAACACCATTTTTAACACCACAACATATATTTCAATCCACGCACCCCAGTGGGGTGCGACTCGGCTTGGTGCCCCATGCGGCTTCCACGGTCTATTTCAATCCACGCACCCCAGTGGGGTGCGACATACGTCTGTGGGTAGCTCTCGTAATCCTCAGCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGTTGACGGCAATCGACGCGACAATGGACGGATTATTTCAATCCACGCACCCCAGTGGGGTGCGACACCCACGGTCTTTTTCCGACACCAGTTCAAGGTCATTTCAATCCACGCACCCCAGTGGGGTGCGACAGCGTGGCATAAGCCACGCGCGTATGATGATACGAATTTCAATCCACGCACCCCAGTGGGGTGCGACGGCTCATCTCCGACGAGGTGGCGCAGGCCAACGAATTTCAATCCACGCACCCCAGTGGGGTGCGACATTCAAAGACCTTGACGCCATCAACGCCGCCAAGATATTTCAATCCACGCACCCCAGTGGGGTGCGACAGAGCTTGGCCGTGTCCACGCCGTCGAACACACACATTTCAATCCACGCACCCCAGTGGGGTGCGACACTGCGGCAAGCATGATTGACGCCGGGATGCCGAATTTCAATCCACGCACCCCAGTGGGGTGCGACTTCAACAGGACACTGCGGATACGACTCCACAGGAATTTCAATCCACGCACCCCAGTGGGGTGCGACCTCACGCCACCGCGTCATCTCGGCGGGGGAGGGATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGTTCGGCCCAGACGCGGACCTTCCCGGAAGCGATTTCAATCCACGCACCCCAGTGGGGTGCGACCGATGGCCTGTGCGGGGTCTCCGCCGGTCTCGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGCCGCAAATGCAAGGCCAGACACATCGCAGCCATTTCAATCCACGCACCCCAGTGGGGTGCGACTCGGGCATAAAAAACCACCCGTGCGGGTGGTTGGGATTTCAATCCACGCACCCCAGTGGGGTGCGACTCGGTGACCGGAACCAACCTGAACGGATCACGGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACAACGGCTATCAATGGACTTTTGACGACATGCTAATTTCAATCCACGCACCCCAGTGGGGTGCGACCGGCGCGATCTGTTCACGTCAGGTTGCAGCACGAGGGAATTTCAATCCACGCACCCCAGTGGGGTGCGACTGAGGGCTTATCATTATCCCCGAACTGCGAGAGATTATTTCAATCCACGCACCCCAGTGGGGTGCGACATTCCCTTGGCTTTTGCGGAACTTCCAACCGCCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACATTCCTGTCGTTGATATCGGGTATGCGCCCCGTGATTTCAATCCACGCACCCCAGTGGGGTGCGACTCTACGGTGAGCTTGGTACGCTGGTCGGCAGTAATATTTCAATCCACGCACCCCAGTGGGGTGCGACGGCATCGAGGCTAGCCAAAGTAAGCTGGGCGCATGATTTCAATCCACGCACCCCAGTGGGGTGCGACGCGCCCTCCTGTCGCGCCGTCAGGAAAGCGAGACGATTTCAATCCACGCACCCCAGTGGGGTGCGACTCTCGCACTGCCCGAGGGGCTGGACACCGGTAGTATTTCAATCCACGCACCCCAGTGGGGTGCGACCATGCGCTATCTCGGAGGAGAGGTCACGGCGCTTATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGTGGCGCGCCGCTCTCGCATACTGGGCGGCATATTTCAATCCACGCACCCCAGTGGGGTGCGACGTCACATAGCAGCTACCGAATGTGACGTCGTGCTGATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTGGCTTCGGCGCTTACCCTTGGCGGTGACGTATTTCAATCCACGCACCCCAGTGGGGTGCGACAGGGTCTCGCTACCGTGTTCCACCGCTCCGACGCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCATGTACTATCATCTGCTACGTGAGCTTGCGTTATTTCAATCCACGCACCCCAGTGGGGTGCGACTACGGCGGCAAAAAACTCATGATAGATGACTGGGTATTTCAATCCACGCACCCCAGTGGGGTGCGACACGCCGGCACCAACATCACCAATCACATTGAAAGATTTCAATCCACGCACCCCAGTGGGGTGCGACATGCGGCCGCGACCTACATCGGCAAGGTGTCGAAATTTCAATCCACGCACCCCAGTGGGGTGCGACAAGATGGCGACGGCACTTCATACGGCTTATACGGATTTCAATCCACGCACCCCAGTGGGGTGCGACTCGTCGATTTACCAGTTCCTGGATCACCATAGATTACATTTCAATCCACGCACCCCAGTGGGGTGCGACTAGACGTGGTGTGGAGGCAGGACAACACCAGTCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCGACCGCCATCGGAATCCCAACCTACGAATAAGATTTCAATCCACGCACCCCAGTGGGGTGCGACGTTCGCCGCATTGGCGGCGGCGTTGAAGCCGATATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGGCGGGGTCCAGGCCACTCCGGTCGGAGCCACATTTCAATCCACGCACCCCAGTGGGGTGCGACGCCATCGCGCGATATGACGGCCAGCCGGACAGGCAATTTCAATCCACGCACCCCAGTGGGGTGCGACCCGTATCGGACTGCAGGACATCATCACCGTCACGATTTCAATCCACGCACCCCAGTGGGGTGCGACTATCCGCTCGCCCAAGAACGGCGGCGACGAACTCATTTCAATCCACGCACCCCAGTGGGGTGCGACCGAGCAGTGGCGCCTGTCCCAATCGGAGGCCGATATTTCAATCCACGCACCCCAGTGGGGTGCGACCGCAACAATGCGATCAGCGACGAGTACCCGGAAGGATTTCAATCCACGCACCCCAGTGGGGTGCGAC

>NZ_CP013673|5|1|1656102-1666931|PILER-CR
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCACGATTCCAAGGATCGTGTCGACCGCTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGTATCCTGCTCTGCCACGCAAAGTGCAGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGAGTGTGAGCGCATACGCCTATGATGCAAGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTAGATAATCGTCTAGGCTGATGTCTTGCGGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGCGGTCATGGTTTCCTCCTTAAAGGATCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCTGCAACTGTCTCACTTGACGTACCGTTTTGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACGCGACTATCAGCCTTGCCATGCTTAGGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGTCAGATACACCGTATCCGCGTACCCGTTATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTAACGGGTGGTGCCCCCGCAGTCCTCAACCTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCCTTCTGATTATCAGTCTTCGTACAGGTCATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGATTATTCACGCCGTTGGCGGGTTCGATACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACGGCACGGCCACGTTCCGGTCGGACGCGGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACAGATAACCAGTTAATCAGCGACACTATGATAGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCCGAACAGTGGCACGGTACAGCAGGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCCCAGGAGGATTCGGCCGAGCGAACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAAACCGTCCTGCAGGCGGGTCGATTGTCCGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCCCACCACGTCCGCCGTGGGGCGCGTTTTCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCGCGACGCCCGATCGGCGGACTCCCACGAGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACGAGGCACAGGAGCCGCAAGGGAACGAGCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCTTCTGGTTCGCGCCGTCGCGTCCGCCAAATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACAAGCGACACGCTCTATTTTTGTTACAGAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGACACCATCATGGACGCCATCATCCCGACCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGCGCGTGGTTTAGGTAAGACATACGGTATAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCTTCACCGATTCAATGAAGGCCAACGTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCGGTCTTGCCGTTTACCTGACCGTCCAAGGG
ATTTCAATCCACGCACCCCAGTAGGGTGCGAC	CACCACCTTGGCGGTAGACCCCGCGCCCGTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTAATTACCGTGTTTGGCGTCCAAACATTGTAATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCGGTTACTTTTTGTAACCGAGTGTGGTATGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACGCCTCTGGGAACGAGCCCTAATAGCCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCGTCGGCTGCCACCTCGCGGTTGTCCACGGGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCAACATCACCACCATCTGGGTGCCGGCGATCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAAAAATCTCACAGCATTAGGCGTAACCGACACC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCTATGGTCGATCAGATTACAGAGATGTATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGGAGGTCAGGGCTCAAACGCTCAAGCTACTTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCTTGTGTTTCCACCCGTCCGGCGCGATGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCTGATTCCACGTGTCCGGCGTGCCGAAAATGGC
ATTTCAACCCACGCACCCCAGTGGGGTGCGAC	GGTGCTTGGGACTTCACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGATCCCGCGTGGCGATGCCGGGACTGCTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGGCGATTCTTTCTTTTTTAGTTGTTCAAGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTTGCCTCTCCGACCACGCGCGGGTCAAACATCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCAAGCCGCAGCGGATAGTGCGAGCAAGGCCGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTACGTTGTCCATCTGAGTTACCAACTGAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCCGCAGTATTGGCATGGTTCGGTGGTGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTTGCTCATTTGAATACTCCTTCGCAGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGCCACGTCCTTGGCGAGGTCCTTGCCCTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCGGAAGCTCAGGTTGTTGAACATGCAGTCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCTGATGATTGGGCCGATCTGCTCGCGGAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCGTTGCTGATGCCCCACAATTGGCCGTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCACGCGCCGTGTTCATTTGCAAGACGATGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCGGGCACGATCTGGCAGTCGCAGTCGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCCATGTCACGCCAGGCACTGCAGCGCATGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCAGCAACCGACGCCTTGCCTACCTTGTCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATGCCCTGGCCGTCGATCTTGCCGACGACGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGACGCGGGTGATGGCACGGGTCACGTCCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATCGTTGTAGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGTAGGGAAACACGTTGTCGTAGGTGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACGCAAGGGCTGTTGATGGCGTCGCCCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCGTTCTGGTTCAGTTCTATGACCTTCTTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCAGGCCCAAAACCGTGGCCACGCCGCCACAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCAATGTCACGGCACCATGTACCGGGCAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATATCACCGCCACGCTGTTCGGCGTGTCCGGCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTGCGGCCGGTTCTCCACACGGTTCACGGTCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCACTCAACCCATTACAGTCTTGTGTGCCAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTGGAGTTAATGCTGAGCGTGGGTAGCATCGTGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTGCTTGGGACTTTACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCACGGTGCCGTCCAGGCCTCTCAATTTCAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTGGTAGGCGCTGTAACGGGTGTTCGTGTCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCAGCAACATCAAGGGATATGTGACCACCGAGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGTCCTTGGCGCGTTTCTCCCATTCGCGGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGGCTGGACGTGACGACGGACGCGACCTTGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AATTACCTTGAGTGAATCGGCCGCGAACTTTGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATTGTTGTGGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACTCGTCCAGCAGCCGAGGGCTTCGTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACACCCTTCTCAGGTGCCATCACACTATCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGTGGGGCCGGTAAGTATCACGTCGGTATTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGCAAGAAGGAAGAGTAACCCATGACCAGCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTGGCTGCCGCCCTCGCTGTGCCCGTCAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAACGCGCGCCGCCAGCCGGCCGGGTCGTCCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGACCGACTGTGCAACGCATTGCGAGTGGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGATGGCTATCACTATACGCGGTCCAATACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACGCCTGTACCTCTCGACCGATTGGGGAGTAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGGTCTTCGACGAGGAGGTCATACCAGTAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTGTTGGCCTGCACGGTGCTCATCTGCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCGCCTGAGTAGGGCGCGCCGTTCTGGATAACT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGGGCATCCCGGCGTCGTTGATGCTCGCGAAGGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGCCGCCCTACGCGAAGAACTTATCGGGCTTATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTGACATCCAGTAAACACTGCCACTGGATCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCCCGGTTATCACACCGGGCTGGTTCATCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGGCTCCATCATAGGTATTCCCAATTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAACCCACGTCGCTTACTGGAGGCTCCAAGCGAGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACTTCGCGGTATCACTACCGCAAGCGGACAGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCGGCCTTGTTCGGGTTGCCGGGGGTGATCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCACGTCGGAGATGGTCTGCTGGTCGGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCACACCGCCGCTCAACCGTTCGCACTCCGCCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACACCACATGCCCCGACCTCGCGCCGAACGGGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTCTTGGCGGCTTACTACAGCAATCAGGTATAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCCTCACATACGCTTCCTGCATCTGCCAAAACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACACCTCATTAGTCACCTGCGTTTTCTGTTGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTTGCGCTCCCCCGTCGCGGTCTGTTTCACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCATAAGCCGGTCTTCTTCGCGCAGCTCACGCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGTATCGAGGGCGTGGACGTGTGTTGGGTGGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACAGGTCAACAACAACTGCCTCGTGTCCGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATACCACGATGCGGCAACAGCCTACTGCCGGTTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCGCTGGTCAAAACGGTTCACCTCCTCGACGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCTTCTGGTTCCCCGTCGGCTTGGCGGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCGCGTCTCTCAAGGAGGCCCAAAGCATCTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCGGGGCTCCGGCTTCGGCGAGGTGCGTGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACTTACTTAATTGAGCTATAATTATTATGTCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGTGTGGCTTGGGTAGGCGTTCCACGCCGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCATGTCGGTGTGCGGCTGCATGGTCATCTGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCGCCACCCGGAACTCACGACAGTCGTTACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACGGCGATCAGCTTTGTCTTCTGGCTCCCTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTGTCTCGTTGACGGATGTGTTGCTGACCTGAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCCGCTTGACGTGCGCTCAATTGAGCGCAACAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGAATCACCGATGCAACCATCACCCTCATCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGAACAAACACCATTTTTAACACCACAACATAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGCTTGGTGCCCCATGCGGCTTCCACGGTCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATACGTCTGTGGGTAGCTCTCGTAATCCTCAGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTGACGGCAATCGACGCGACAATGGACGGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCCACGGTCTTTTTCCGACACCAGTTCAAGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGTGGCATAAGCCACGCGCGTATGATGATACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCTCATCTCCGACGAGGTGGCGCAGGCCAACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCAAAGACCTTGACGCCATCAACGCCGCCAAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGCTTGGCCGTGTCCACGCCGTCGAACACACAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACTGCGGCAAGCATGATTGACGCCGGGATGCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCAACAGGACACTGCGGATACGACTCCACAGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCACGCCACCGCGTCATCTCGGCGGGGGAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTTCGGCCCAGACGCGGACCTTCCCGGAAGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGATGGCCTGTGCGGGGTCTCCGCCGGTCTCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCGCAAATGCAAGGCCAGACACATCGCAGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGGCATAAAAAACCACCCGTGCGGGTGGTTGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGACCGGAACCAACCTGAACGGATCACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACGGCTATCAATGGACTTTTGACGACATGCTA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGCGCGATCTGTTCACGTCAGGTTGCAGCACGAGGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGAGGGCTTATCATTATCCCCGAACTGCGAGAGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCCTTGGCTTTTGCGGAACTTCCAACCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCTGTCGTTGATATCGGGTATGCGCCCCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTACGGTGAGCTTGGTACGCTGGTCGGCAGTAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCATCGAGGCTAGCCAAAGTAAGCTGGGCGCATG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCCCTCCTGTCGCGCCGTCAGGAAAGCGAGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTCGCACTGCCCGAGGGGCTGGACACCGGTAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCGCTATCTCGGAGGAGAGGTCACGGCGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTGGCGCGCCGCTCTCGCATACTGGGCGGCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCACATAGCAGCTACCGAATGTGACGTCGTGCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGGCTTCGGCGCTTACCCTTGGCGGTGACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGGGTCTCGCTACCGTGTTCCACCGCTCCGACGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGTACTATCATCTGCTACGTGAGCTTGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACGGCGGCAAAAAACTCATGATAGATGACTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGCCGGCACCAACATCACCAATCACATTGAAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGGCCGCGACCTACATCGGCAAGGTGTCGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGATGGCGACGGCACTTCATACGGCTTATACGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGTCGATTTACCAGTTCCTGGATCACCATAGATTAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAGACGTGGTGTGGAGGCAGGACAACACCAGTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACCGCCATCGGAATCCCAACCTACGAATAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTCGCCGCATTGGCGGCGGCGTTGAAGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCGGGGTCCAGGCCACTCCGGTCGGAGCCAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCATCGCGCGATATGACGGCCAGCCGGACAGGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTATCGGACTGCAGGACATCATCACCGTCACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCCGCTCGCCCAAGAACGGCGGCGACGAACTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAGCAGTGGCGCCTGTCCCAATCGGAGGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACAATGCGATCAGCGACGAGTACCCGGAAGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC

>NZ_CP013673|5|5|1656102-1666931|CRISPRCasFinder
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCACGATTCCAAGGATCGTGTCGACCGCTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGTATCCTGCTCTGCCACGCAAAGTGCAGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGAGTGTGAGCGCATACGCCTATGATGCAAGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTAGATAATCGTCTAGGCTGATGTCTTGCGGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGCGGTCATGGTTTCCTCCTTAAAGGATCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCTGCAACTGTCTCACTTGACGTACCGTTTTGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACGCGACTATCAGCCTTGCCATGCTTAGGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGTCAGATACACCGTATCCGCGTACCCGTTATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTAACGGGTGGTGCCCCCGCAGTCCTCAACCTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCCTTCTGATTATCAGTCTTCGTACAGGTCATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGATTATTCACGCCGTTGGCGGGTTCGATACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACGGCACGGCCACGTTCCGGTCGGACGCGGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACAGATAACCAGTTAATCAGCGACACTATGATAGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCCGAACAGTGGCACGGTACAGCAGGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCCCAGGAGGATTCGGCCGAGCGAACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAAACCGTCCTGCAGGCGGGTCGATTGTCCGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCCCACCACGTCCGCCGTGGGGCGCGTTTTCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCGCGACGCCCGATCGGCGGACTCCCACGAGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACGAGGCACAGGAGCCGCAAGGGAACGAGCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCTTCTGGTTCGCGCCGTCGCGTCCGCCAAATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACAAGCGACACGCTCTATTTTTGTTACAGAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGACACCATCATGGACGCCATCATCCCGACCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGCGCGTGGTTTAGGTAAGACATACGGTATAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCTTCACCGATTCAATGAAGGCCAACGTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCGGTCTTGCCGTTTACCTGACCGTCCAAGGG
ATTTCAATCCACGCACCCCAGTAGGGTGCGAC	CACCACCTTGGCGGTAGACCCCGCGCCCGTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTAATTACCGTGTTTGGCGTCCAAACATTGTAATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCGGTTACTTTTTGTAACCGAGTGTGGTATGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACGCCTCTGGGAACGAGCCCTAATAGCCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCGTCGGCTGCCACCTCGCGGTTGTCCACGGGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCAACATCACCACCATCTGGGTGCCGGCGATCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAAAAATCTCACAGCATTAGGCGTAACCGACACC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCTATGGTCGATCAGATTACAGAGATGTATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGGAGGTCAGGGCTCAAACGCTCAAGCTACTTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCTTGTGTTTCCACCCGTCCGGCGCGATGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCTGATTCCACGTGTCCGGCGTGCCGAAAATGGC
ATTTCAACCCACGCACCCCAGTGGGGTGCGAC	GGTGCTTGGGACTTCACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGATCCCGCGTGGCGATGCCGGGACTGCTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGGCGATTCTTTCTTTTTTAGTTGTTCAAGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTTGCCTCTCCGACCACGCGCGGGTCAAACATCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCAAGCCGCAGCGGATAGTGCGAGCAAGGCCGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTACGTTGTCCATCTGAGTTACCAACTGAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCCGCAGTATTGGCATGGTTCGGTGGTGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTTGCTCATTTGAATACTCCTTCGCAGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGCCACGTCCTTGGCGAGGTCCTTGCCCTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCGGAAGCTCAGGTTGTTGAACATGCAGTCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCTGATGATTGGGCCGATCTGCTCGCGGAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCGTTGCTGATGCCCCACAATTGGCCGTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCACGCGCCGTGTTCATTTGCAAGACGATGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCGGGCACGATCTGGCAGTCGCAGTCGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCCATGTCACGCCAGGCACTGCAGCGCATGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCAGCAACCGACGCCTTGCCTACCTTGTCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATGCCCTGGCCGTCGATCTTGCCGACGACGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGACGCGGGTGATGGCACGGGTCACGTCCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATCGTTGTAGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGTAGGGAAACACGTTGTCGTAGGTGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACGCAAGGGCTGTTGATGGCGTCGCCCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCGTTCTGGTTCAGTTCTATGACCTTCTTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCAGGCCCAAAACCGTGGCCACGCCGCCACAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCAATGTCACGGCACCATGTACCGGGCAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATATCACCGCCACGCTGTTCGGCGTGTCCGGCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTGCGGCCGGTTCTCCACACGGTTCACGGTCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCACTCAACCCATTACAGTCTTGTGTGCCAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTGGAGTTAATGCTGAGCGTGGGTAGCATCGTGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTGCTTGGGACTTTACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCACGGTGCCGTCCAGGCCTCTCAATTTCAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTGGTAGGCGCTGTAACGGGTGTTCGTGTCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCAGCAACATCAAGGGATATGTGACCACCGAGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGTCCTTGGCGCGTTTCTCCCATTCGCGGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGGCTGGACGTGACGACGGACGCGACCTTGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AATTACCTTGAGTGAATCGGCCGCGAACTTTGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATTGTTGTGGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACTCGTCCAGCAGCCGAGGGCTTCGTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACACCCTTCTCAGGTGCCATCACACTATCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGTGGGGCCGGTAAGTATCACGTCGGTATTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGCAAGAAGGAAGAGTAACCCATGACCAGCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTGGCTGCCGCCCTCGCTGTGCCCGTCAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAACGCGCGCCGCCAGCCGGCCGGGTCGTCCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGACCGACTGTGCAACGCATTGCGAGTGGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGATGGCTATCACTATACGCGGTCCAATACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACGCCTGTACCTCTCGACCGATTGGGGAGTAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGGTCTTCGACGAGGAGGTCATACCAGTAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTGTTGGCCTGCACGGTGCTCATCTGCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCGCCTGAGTAGGGCGCGCCGTTCTGGATAACT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGGGCATCCCGGCGTCGTTGATGCTCGCGAAGGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGCCGCCCTACGCGAAGAACTTATCGGGCTTATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTGACATCCAGTAAACACTGCCACTGGATCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCCCGGTTATCACACCGGGCTGGTTCATCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGGCTCCATCATAGGTATTCCCAATTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAACCCACGTCGCTTACTGGAGGCTCCAAGCGAGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACTTCGCGGTATCACTACCGCAAGCGGACAGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCGGCCTTGTTCGGGTTGCCGGGGGTGATCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCACGTCGGAGATGGTCTGCTGGTCGGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCACACCGCCGCTCAACCGTTCGCACTCCGCCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACACCACATGCCCCGACCTCGCGCCGAACGGGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTCTTGGCGGCTTACTACAGCAATCAGGTATAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCCTCACATACGCTTCCTGCATCTGCCAAAACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACACCTCATTAGTCACCTGCGTTTTCTGTTGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTTGCGCTCCCCCGTCGCGGTCTGTTTCACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCATAAGCCGGTCTTCTTCGCGCAGCTCACGCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGTATCGAGGGCGTGGACGTGTGTTGGGTGGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACAGGTCAACAACAACTGCCTCGTGTCCGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATACCACGATGCGGCAACAGCCTACTGCCGGTTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCGCTGGTCAAAACGGTTCACCTCCTCGACGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCTTCTGGTTCCCCGTCGGCTTGGCGGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCGCGTCTCTCAAGGAGGCCCAAAGCATCTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCGGGGCTCCGGCTTCGGCGAGGTGCGTGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACTTACTTAATTGAGCTATAATTATTATGTCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGTGTGGCTTGGGTAGGCGTTCCACGCCGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCATGTCGGTGTGCGGCTGCATGGTCATCTGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCGCCACCCGGAACTCACGACAGTCGTTACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACGGCGATCAGCTTTGTCTTCTGGCTCCCTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTGTCTCGTTGACGGATGTGTTGCTGACCTGAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCCGCTTGACGTGCGCTCAATTGAGCGCAACAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGAATCACCGATGCAACCATCACCCTCATCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGAACAAACACCATTTTTAACACCACAACATAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGCTTGGTGCCCCATGCGGCTTCCACGGTCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATACGTCTGTGGGTAGCTCTCGTAATCCTCAGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTGACGGCAATCGACGCGACAATGGACGGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCCACGGTCTTTTTCCGACACCAGTTCAAGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGTGGCATAAGCCACGCGCGTATGATGATACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCTCATCTCCGACGAGGTGGCGCAGGCCAACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCAAAGACCTTGACGCCATCAACGCCGCCAAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGCTTGGCCGTGTCCACGCCGTCGAACACACAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACTGCGGCAAGCATGATTGACGCCGGGATGCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCAACAGGACACTGCGGATACGACTCCACAGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCACGCCACCGCGTCATCTCGGCGGGGGAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTTCGGCCCAGACGCGGACCTTCCCGGAAGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGATGGCCTGTGCGGGGTCTCCGCCGGTCTCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCGCAAATGCAAGGCCAGACACATCGCAGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGGCATAAAAAACCACCCGTGCGGGTGGTTGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGACCGGAACCAACCTGAACGGATCACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACGGCTATCAATGGACTTTTGACGACATGCTA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGCGCGATCTGTTCACGTCAGGTTGCAGCACGAGGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGAGGGCTTATCATTATCCCCGAACTGCGAGAGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCCTTGGCTTTTGCGGAACTTCCAACCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCTGTCGTTGATATCGGGTATGCGCCCCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTACGGTGAGCTTGGTACGCTGGTCGGCAGTAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCATCGAGGCTAGCCAAAGTAAGCTGGGCGCATG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCCCTCCTGTCGCGCCGTCAGGAAAGCGAGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTCGCACTGCCCGAGGGGCTGGACACCGGTAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCGCTATCTCGGAGGAGAGGTCACGGCGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTGGCGCGCCGCTCTCGCATACTGGGCGGCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCACATAGCAGCTACCGAATGTGACGTCGTGCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGGCTTCGGCGCTTACCCTTGGCGGTGACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGGGTCTCGCTACCGTGTTCCACCGCTCCGACGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGTACTATCATCTGCTACGTGAGCTTGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACGGCGGCAAAAAACTCATGATAGATGACTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGCCGGCACCAACATCACCAATCACATTGAAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGGCCGCGACCTACATCGGCAAGGTGTCGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGATGGCGACGGCACTTCATACGGCTTATACGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGTCGATTTACCAGTTCCTGGATCACCATAGATTAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAGACGTGGTGTGGAGGCAGGACAACACCAGTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACCGCCATCGGAATCCCAACCTACGAATAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTCGCCGCATTGGCGGCGGCGTTGAAGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCGGGGTCCAGGCCACTCCGGTCGGAGCCAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCATCGCGCGATATGACGGCCAGCCGGACAGGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTATCGGACTGCAGGACATCATCACCGTCACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCCGCTCGCCCAAGAACGGCGGCGACGAACTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAGCAGTGGCGCCTGTCCCAATCGGAGGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACAATGCGATCAGCGACGAGTACCCGGAAGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC

>NZ_CP013673|5|1|1656102-1666931|CRT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCACGATTCCAAGGATCGTGTCGACCGCTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGTATCCTGCTCTGCCACGCAAAGTGCAGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGAGTGTGAGCGCATACGCCTATGATGCAAGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTAGATAATCGTCTAGGCTGATGTCTTGCGGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGCGGTCATGGTTTCCTCCTTAAAGGATCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCTGCAACTGTCTCACTTGACGTACCGTTTTGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACGCGACTATCAGCCTTGCCATGCTTAGGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGTCAGATACACCGTATCCGCGTACCCGTTATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTAACGGGTGGTGCCCCCGCAGTCCTCAACCTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCCTTCTGATTATCAGTCTTCGTACAGGTCATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGATTATTCACGCCGTTGGCGGGTTCGATACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACGGCACGGCCACGTTCCGGTCGGACGCGGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACAGATAACCAGTTAATCAGCGACACTATGATAGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCCGAACAGTGGCACGGTACAGCAGGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCCCAGGAGGATTCGGCCGAGCGAACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAAACCGTCCTGCAGGCGGGTCGATTGTCCGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCCCACCACGTCCGCCGTGGGGCGCGTTTTCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCGCGACGCCCGATCGGCGGACTCCCACGAGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACGAGGCACAGGAGCCGCAAGGGAACGAGCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCTTCTGGTTCGCGCCGTCGCGTCCGCCAAATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACAAGCGACACGCTCTATTTTTGTTACAGAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGACACCATCATGGACGCCATCATCCCGACCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCGCGCGTGGTTTAGGTAAGACATACGGTATAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCTTCACCGATTCAATGAAGGCCAACGTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACCGGTCTTGCCGTTTACCTGACCGTCCAAGGG
ATTTCAATCCACGCACCCCAGTAGGGTGCGAC	CACCACCTTGGCGGTAGACCCCGCGCCCGTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTAATTACCGTGTTTGGCGTCCAAACATTGTAATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCGGTTACTTTTTGTAACCGAGTGTGGTATGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACGCCTCTGGGAACGAGCCCTAATAGCCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCGTCGGCTGCCACCTCGCGGTTGTCCACGGGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCAACATCACCACCATCTGGGTGCCGGCGATCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAAAAATCTCACAGCATTAGGCGTAACCGACACC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCTATGGTCGATCAGATTACAGAGATGTATGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGGAGGTCAGGGCTCAAACGCTCAAGCTACTTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCTTGTGTTTCCACCCGTCCGGCGCGATGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCTGATTCCACGTGTCCGGCGTGCCGAAAATGGC
ATTTCAACCCACGCACCCCAGTGGGGTGCGAC	GGTGCTTGGGACTTCACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGATCCCGCGTGGCGATGCCGGGACTGCTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCGGCCTTCTTGCTGGCGGCTTCCTTGTCGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGGCGATTCTTTCTTTTTTAGTTGTTCAAGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTTGCCTCTCCGACCACGCGCGGGTCAAACATCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCAAGCCGCAGCGGATAGTGCGAGCAAGGCCGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTACGTTGTCCATCTGAGTTACCAACTGAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCCGCAGTATTGGCATGGTTCGGTGGTGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTTGCTCATTTGAATACTCCTTCGCAGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGCCACGTCCTTGGCGAGGTCCTTGCCCTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGGCGGAAGCTCAGGTTGTTGAACATGCAGTCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCTGATGATTGGGCCGATCTGCTCGCGGAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCGTTGCTGATGCCCCACAATTGGCCGTTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCACGCGCCGTGTTCATTTGCAAGACGATGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCGGGCACGATCTGGCAGTCGCAGTCGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCCATGTCACGCCAGGCACTGCAGCGCATGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCAGCAACCGACGCCTTGCCTACCTTGTCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATGCCCTGGCCGTCGATCTTGCCGACGACGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGACGCGGGTGATGGCACGGGTCACGTCCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATCGTTGTAGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGTAGGGAAACACGTTGTCGTAGGTGTCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACGCAAGGGCTGTTGATGGCGTCGCCCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAACCGTTCTGGTTCAGTTCTATGACCTTCTTGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCAGGCCCAAAACCGTGGCCACGCCGCCACAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCAATGTCACGGCACCATGTACCGGGCAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATATCACCGCCACGCTGTTCGGCGTGTCCGGCAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTGCGGCCGGTTCTCCACACGGTTCACGGTCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCCACTCAACCCATTACAGTCTTGTGTGCCAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTGGAGTTAATGCTGAGCGTGGGTAGCATCGTGGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTGCTTGGGACTTTACGATTCCCGTGGGTGTCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCACGGTGCCGTCCAGGCCTCTCAATTTCAGCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCTGGTAGGCGCTGTAACGGGTGTTCGTGTCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCCAGCAACATCAAGGGATATGTGACCACCGAGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGTCCTTGGCGCGTTTCTCCCATTCGCGGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGGCTGGACGTGACGACGGACGCGACCTTGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AATTACCTTGAGTGAATCGGCCGCGAACTTTGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCATGGCTTTCCAAGATTGTTGTGGCCTTCATCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CACTCGTCCAGCAGCCGAGGGCTTCGTGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAACACACCCTTCTCAGGTGCCATCACACTATCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGTGGGGCCGGTAAGTATCACGTCGGTATTCCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CAGCAAGAAGGAAGAGTAACCCATGACCAGCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTCTGGCTGCCGCCCTCGCTGTGCCCGTCAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAACGCGCGCCGCCAGCCGGCCGGGTCGTCCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTCGACCGACTGTGCAACGCATTGCGAGTGGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGATGGCTATCACTATACGCGGTCCAATACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACGCCTGTACCTCTCGACCGATTGGGGAGTAGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGGTCTTCGACGAGGAGGTCATACCAGTAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTGTTGGCCTGCACGGTGCTCATCTGCTGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCGCCTGAGTAGGGCGCGCCGTTCTGGATAACT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGGGCATCCCGGCGTCGTTGATGCTCGCGAAGGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGGCCGCCCTACGCGAAGAACTTATCGGGCTTATC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTGACATCCAGTAAACACTGCCACTGGATCGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCCCGGTTATCACACCGGGCTGGTTCATCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTGTTGGCTCCATCATAGGTATTCCCAATTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAACCCACGTCGCTTACTGGAGGCTCCAAGCGAGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACTTCGCGGTATCACTACCGCAAGCGGACAGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCGGCCTTGTTCGGGTTGCCGGGGGTGATCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATCACGTCGGAGATGGTCTGCTGGTCGGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCACACCGCCGCTCAACCGTTCGCACTCCGCCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACACCACATGCCCCGACCTCGCGCCGAACGGGCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTCTTGGCGGCTTACTACAGCAATCAGGTATAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCCCTCACATACGCTTCCTGCATCTGCCAAAACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACACCTCATTAGTCACCTGCGTTTTCTGTTGGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTTGCGCTCCCCCGTCGCGGTCTGTTTCACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCATAAGCCGGTCTTCTTCGCGCAGCTCACGCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGTATCGAGGGCGTGGACGTGTGTTGGGTGGAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GACAGGTCAACAACAACTGCCTCGTGTCCGGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATACCACGATGCGGCAACAGCCTACTGCCGGTTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGCGCTGGTCAAAACGGTTCACCTCCTCGACGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCAGCTTCTGGTTCCCCGTCGGCTTGGCGGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATCGCGTCTCTCAAGGAGGCCCAAAGCATCTGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCCGGGGCTCCGGCTTCGGCGAGGTGCGTGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACTTACTTAATTGAGCTATAATTATTATGTCAAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGTGTGGCTTGGGTAGGCGTTCCACGCCGTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCATGTCGGTGTGCGGCTGCATGGTCATCTGCGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCGCCACCCGGAACTCACGACAGTCGTTACTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGACGGCGATCAGCTTTGTCTTCTGGCTCCCTGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GATTGTCTCGTTGACGGATGTGTTGCTGACCTGAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCCGCTTGACGTGCGCTCAATTGAGCGCAACAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GAGGAATCACCGATGCAACCATCACCCTCATCCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGAACAAACACCATTTTTAACACCACAACATAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGCTTGGTGCCCCATGCGGCTTCCACGGTCT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATACGTCTGTGGGTAGCTCTCGTAATCCTCAGC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGTTGACGGCAATCGACGCGACAATGGACGGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACCCACGGTCTTTTTCCGACACCAGTTCAAGGTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGCGTGGCATAAGCCACGCGCGTATGATGATACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCTCATCTCCGACGAGGTGGCGCAGGCCAACGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCAAAGACCTTGACGCCATCAACGCCGCCAAGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGAGCTTGGCCGTGTCCACGCCGTCGAACACACAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACTGCGGCAAGCATGATTGACGCCGGGATGCCGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TTCAACAGGACACTGCGGATACGACTCCACAGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CTCACGCCACCGCGTCATCTCGGCGGGGGAGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGTTCGGCCCAGACGCGGACCTTCCCGGAAGCG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGATGGCCTGTGCGGGGTCTCCGCCGGTCTCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGCCGCAAATGCAAGGCCAGACACATCGCAGCC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGGCATAAAAAACCACCCGTGCGGGTGGTTGGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGGTGACCGGAACCAACCTGAACGGATCACGGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AACGGCTATCAATGGACTTTTGACGACATGCTA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGGCGCGATCTGTTCACGTCAGGTTGCAGCACGAGGGA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TGAGGGCTTATCATTATCCCCGAACTGCGAGAGATT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCCTTGGCTTTTGCGGAACTTCCAACCGCCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATTCCTGTCGTTGATATCGGGTATGCGCCCCGTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTACGGTGAGCTTGGTACGCTGGTCGGCAGTAAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GGCATCGAGGCTAGCCAAAGTAAGCTGGGCGCATG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCGCCCTCCTGTCGCGCCGTCAGGAAAGCGAGACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCTCGCACTGCCCGAGGGGCTGGACACCGGTAGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGCGCTATCTCGGAGGAGAGGTCACGGCGCTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTGGCGCGCCGCTCTCGCATACTGGGCGGCAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTCACATAGCAGCTACCGAATGTGACGTCGTGCTG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTGGCTTCGGCGCTTACCCTTGGCGGTGACGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AGGGTCTCGCTACCGTGTTCCACCGCTCCGACGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CATGTACTATCATCTGCTACGTGAGCTTGCGTT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TACGGCGGCAAAAAACTCATGATAGATGACTGGGT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ACGCCGGCACCAACATCACCAATCACATTGAAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	ATGCGGCCGCGACCTACATCGGCAAGGTGTCGAA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	AAGATGGCGACGGCACTTCATACGGCTTATACGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TCGTCGATTTACCAGTTCCTGGATCACCATAGATTAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TAGACGTGGTGTGGAGGCAGGACAACACCAGTCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGACCGCCATCGGAATCCCAACCTACGAATAAG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GTTCGCCGCATTGGCGGCGGCGTTGAAGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGGCGGGGTCCAGGCCACTCCGGTCGGAGCCAC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	GCCATCGCGCGATATGACGGCCAGCCGGACAGGCA
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CCGTATCGGACTGCAGGACATCATCACCGTCACG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	TATCCGCTCGCCCAAGAACGGCGGCGACGAACTC
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGAGCAGTGGCGCCTGTCCCAATCGGAGGCCGAT
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC	CGCAACAATGCGATCAGCGACGAGTACCCGGAAGG
ATTTCAATCCACGCACCCCAGTGGGGTGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_007053158.1\|1654202_1654487_+\|DNA-directed-RNA-polymerase-subunit-omega	unknown	unknown	gnl\|CDD\|234744
NZ_CP013673.1\|WP_058102096.1\|1672988_1675427_-\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
NZ_CP013673.1\|WP_058102102.1\|1672277_1672982_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|187782
NZ_CP013673.1\|WP_058101921.1\|1651060_1652047_+\|methionyl-tRNA-formyltransferase	unknown	unknown	gnl\|CDD\|234567
NZ_CP013673.1\|WP_011068843.1\|1647169_1647922_+\|phosphoserine-phosphatase-SerB	unknown	unknown	gnl\|CDD\|319803
NZ_CP013673.1\|WP_041080761.1\|1654764_1655985_+\|methionine-adenosyltransferase	unknown	unknown	gnl\|CDD\|235374
NZ_CP013673.1\|WP_013141141.1\|1650332_1651037_+\|HAD-family-phosphatase	unknown	unknown	gnl\|CDD\|319790
NZ_CP013673.1\|WP_116868976.1\|1676105_1676327_-\|transposase	unknown	unknown	gnl\|CDD\|376574
NZ_CP013673.1\|WP_058102097.1\|1670316_1672275_-\|CRISPR-associated-protein-Cas8	cas8c	pfam09709_cas8c_CAS-I-C	gnl\|CDD\|378245
NZ_CP013673.1\|WP_058101923.1\|1644824_1646390_-\|proteasome-ATPase	unknown	unknown	gnl\|CDD\|200312
NZ_CP013673.1\|WP_058102100.1\|1667317_1667608_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP013673.1\|WP_063124480.1\|1652138_1654001_-\|dihydroxy-acid-dehydratase	unknown	unknown	gnl\|CDD\|237104
NZ_CP013673.1\|WP_058101922.1\|1647961_1650274_+\|primosomal-protein-N'	unknown	unknown	gnl\|CDD\|237844
NZ_CP013673.1\|WP_058102099.1\|1667693_1668725_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP013673.1\|WP_013410712.1\|1680954_1682166_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|224090
NZ_CP013673.1\|WP_058101924.1\|1643135_1644803_-\|proteasome-accessory-factor-PafA2	unknown	unknown	gnl\|CDD\|274726
NZ_CP013673.1\|WP_058102094.1\|1677049_1680361_-\|mupirocin-resistant-isoleucine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235681
NZ_CP013673.1\|WP_058102098.1\|1668721_1669423_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|273040
NZ_CP013673.1\|WP_007055597.1\|1646450_1647149_-\|DedA-family-protein	unknown	unknown	gnl\|CDD\|223659
NZ_CP013673.1\|WP_014484099.1\|1669461_1670313_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl\|CDD\|187820

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_007053158.1\|1654202_1654487_+\|DNA-directed-RNA-polymerase-subunit-omega	gnl\|CDD\|234744	PRK00392, rpoZ, DNA-directed RNA polymerase subunit omega; Reviewed.	3.15482e-17
NZ_CP013673.1\|WP_058102096.1\|1672988_1675427_-\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	1.21001e-48
NZ_CP013673.1\|WP_058102102.1\|1672277_1672982_-\|type-I-C-CRISPR-associated-protein-Cas5	gnl\|CDD\|187782	cd09651, Cas5_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas5. 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; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex; in subtype I-C this protein might be the endoribonuclease that generates crRNAs; also known as DevS family.	7.4959e-84
NZ_CP013673.1\|WP_058101921.1\|1651060_1652047_+\|methionyl-tRNA-formyltransferase	gnl\|CDD\|234567	PRK00005, fmt, methionyl-tRNA formyltransferase; Reviewed.	3.80669e-127
NZ_CP013673.1\|WP_011068843.1\|1647169_1647922_+\|phosphoserine-phosphatase-SerB	gnl\|CDD\|319803	cd07500, HAD_PSP, phosphoserine phosphatase (PSP), similar to Methanococcus Jannaschii PSP and Saccharomyces cerevisiae SER2p. This family includes Methanococcus jannaschii PSP, and Saccharomyces cerevisiae phosphoserine phosphatase SER2p, EC 3.1.3.3, which participates in a pathway whereby serine and glycine are synthesized from the glycolytic intermediate 3-phosphoglycerate; phosphoserine phosphatase catalyzes the hydrolysis of phospho-L-serine to L-serine and inorganic phosphate, the third reaction in this pathway. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	7.32125e-103
NZ_CP013673.1\|WP_041080761.1\|1654764_1655985_+\|methionine-adenosyltransferase	gnl\|CDD\|235374	PRK05250, PRK05250, S-adenosylmethionine synthetase; Validated.	0
NZ_CP013673.1\|WP_013141141.1\|1650332_1651037_+\|HAD-family-phosphatase	gnl\|CDD\|319790	cd02603, HAD_sEH-N_like, N-terminal lipase phosphatase domain of human soluble epoxide hydrolase, Escherichia coli YihX/HAD4 alpha-D-glucose 1-phosphate phosphatase, and related domains, may be inactive. This family includes the N-terminal phosphatase domain of human soluble epoxide hydrolase (sEH). sEH is a bifunctional enzyme with two distinct enzyme activities, the C-terminal domain has epoxide hydrolysis activity and the N-terminal domain (Ntermphos), which belongs to this family, has lipid phosphatase activity. The latter prefers mono-phosphate esters, and lysophosphatidic acids (LPAs) are the best natural substrates found to date. In addition this family includes Gallus gallus sEH and Xenopus sEH which appears to lack phosphatase activity, and Escherichia coli YihX/HAD4 which selectively hydrolyzes alpha-Glucose-1-P, phosphatase, has significant phosphatase activity against pyridoxal phosphate, and has low beta phosphoglucomutase activity. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	3.04868e-45
NZ_CP013673.1\|WP_116868976.1\|1676105_1676327_-\|transposase	gnl\|CDD\|376574	pfam01610, DDE_Tnp_ISL3, Transposase. Transposase proteins are necessary for efficient DNA transposition. Contains transposases for IS204, IS1001, IS1096 and IS1165.	3.6478e-14
NZ_CP013673.1\|WP_058102097.1\|1670316_1672275_-\|CRISPR-associated-protein-Cas8	gnl\|CDD\|378245	pfam09709, Cas_Csd1, CRISPR-associated protein (Cas_Csd1). CRISPR loci appear to be mobile elements with a wide host range. This entry represents proteins that tend to be found near CRISPR repeats. The species range, so far, is exclusively bacterial and mesophilic, although CRISPR loci are particularly common among the archaea and thermophilic bacteria. Clusters of short DNA repeats with nonhomologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins.	1.89191e-88
NZ_CP013673.1\|WP_058101923.1\|1644824_1646390_-\|proteasome-ATPase	gnl\|CDD\|200312	TIGR03689, pup_AAA, proteasome ATPase. In the Actinobacteria, as shown for Mycobacterium tuberculosis, some proteins are modified by ligation between an epsilon-amino group of a lysine side chain and the C-terminal carboxylate of the ubiquitin-like protein Pup. This modification leads to protein degradation by the archaeal-like proteasome found in the Actinobacteria. Members of this protein family belong to the AAA family of ATPases and tend to be clustered with the genes for Pup, the Pup ligase PafA, and structural components of the proteasome. This protein forms hexameric rings with ATPase activity. [Protein fate, Degradation of proteins, peptides, and glycopeptides].	0
NZ_CP013673.1\|WP_058102100.1\|1667317_1667608_-\|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.	2.70436e-29
NZ_CP013673.1\|WP_063124480.1\|1652138_1654001_-\|dihydroxy-acid-dehydratase	gnl\|CDD\|237104	PRK12448, PRK12448, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP013673.1\|WP_058101922.1\|1647961_1650274_+\|primosomal-protein-N'	gnl\|CDD\|237844	PRK14873, PRK14873, primosomal protein N'.	0
NZ_CP013673.1\|WP_058102099.1\|1667693_1668725_-\|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.	6.35209e-175
NZ_CP013673.1\|WP_013410712.1\|1680954_1682166_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|224090	COG1168, MalY, Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities [Amino acid transport and metabolism].	5.78153e-110
NZ_CP013673.1\|WP_058101924.1\|1643135_1644803_-\|proteasome-accessory-factor-PafA2	gnl\|CDD\|274726	TIGR03688, pupylate_PafA2, proteasome accessory factor PafA2. This protein family is paralogous to (and distinct from) the PafA (proteasome accessory factor) first described in Mycobacterium tuberculosis (see TIGR03686). Members of both this family and TIGR03686 itself tend to cluster with each other, with the ubiquitin analog Pup (TIGR03687) associated with targeting to the proteasome, and with proteasome subunits themselves. [Protein fate, Degradation of proteins, peptides, and glycopeptides].	0
NZ_CP013673.1\|WP_058102094.1\|1677049_1680361_-\|mupirocin-resistant-isoleucine--tRNA-ligase	gnl\|CDD\|235681	PRK06039, ileS, isoleucyl-tRNA synthetase; Reviewed.	0
NZ_CP013673.1\|WP_058102098.1\|1668721_1669423_-\|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.	9.25583e-32
NZ_CP013673.1\|WP_007055597.1\|1646450_1647149_-\|DedA-family-protein	gnl\|CDD\|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	6.0427e-43
NZ_CP013673.1\|WP_014484099.1\|1669461_1670313_-\|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.	2.89068e-107

>NZ_CP013673.1|WP_041080761.1|1654764_1655985_+|methionine-adenosyltransferase
MTEEHRLISAESVTEGHPDKVCDQISDAILDDLLAQDSSSHVAVETSAATGVFLIFGEVTSKGYCDVQSKVRETLRNIGYTSSEVGLDADSCGVVVAITEQSAEINQGVARLTGDQETAASREERYEAQGAGDQGVMFGYATDETPTLMPLPIYLAHRLAFRLTEVRKSGEVPHLRPDGKTQVTIEYDDDDKPVRLDTVLISTQHDPEVTQDWLAVELKKHVIDPVLDEVLGSKVPHDNYRQLVNPTGSFILGGPAADAGLTGRKIIVDTYGGAAHHGGGAFSGKDPSKVDRSAAYATRWVAKNIVAAGLAHKVEIQIAYAIGVADPVSVNVETFGTEQGVTRGQIAAAVRKVFDLRPAAIIDELDLKRPIYLKTAAYGHFGRTDVEFPWEKTDKVEELKAAIAGE
>NZ_CP013673.1|WP_007053158.1|1654202_1654487_+|DNA-directed-RNA-polymerase-subunit-omega
MAFGTDPTPDGLANPPIDDLMKHADSKYALAIFAAKRARQINSYFTQLNEGLLQNIGPLVEYQNNEKPLSIAFREIDEGLLEETLGEDDANEGN
>NZ_CP013673.1|WP_063124480.1|1652138_1654001_-|dihydroxy-acid-dehydratase
MTEMRSAKIMSGRVFAGARALYRAAGVSGDDMGKKPIIAIANSFDEFLPGHVHLNKVGRIVSEAIKEAGGIPREFNTMAVDDGIAMGHTGMLYSLPSRDIIADTVEYQCNAHCADALICIPNCDKVVPGMLMAALRLNIPTVFVSGGPMEAGTTVLADGTVKSTDLIDVMYATADDNVSDEELLNYEKTVCPTCGSCAGMFTANSMNCLTEAIGLALPGNGTILASHSYRKDLFKRAAKQVVKIAHQYYDDSDDSVLPRSIATKEAFENAMTMDVAMGGSTNTVLHILAMAQSADVDFTLDDIERISHTVPCICKASPSGKWEISDVHRAGGITGILGELDRAGKLHTNVHSIDYPTLEAKLADWDIMRPTCTEEAQQMYKAAPGHIISPEPWTHTTLFDSLDRDRTNGAIHDINHPEIHEGGLAVLRGNLAPDGCVVKTAGVPPEIWKFRGPALVVDSQEQAIEVILNDTLKPGMALVIRYEGPKGGPGMQEMLYPTSFVKGKGIGKQVAMLTDGRYSGGSSGLAIGHMAPEAANKGPVALIKNGDIIDIDIEARSVNVELTDEQLDERRRELEAGDGYVAHRNRHVSQALKAYAAFARSADKGATRDPELINKLSGLN
>NZ_CP013673.1|WP_058101921.1|1651060_1652047_+|methionyl-tRNA-formyltransferase
MLKLVFAGTPDVAVPSLKAFAADPRFDVVGVITRPDAPTGRGRKLTPSPVKATALELGLPVIDLKPRSPEFMEALNDLHADIAAVIAYGNILPKNVLDAVPMGWYNLHFSNLPKWRGAAPAQRAIWAGDPTTGADVFKVGEGLDDGPIVASLTIELTGRETSGELLDRLAEEGAPMYVDALAAVGEGTATFTAQPAESLEYAHKITVEDARISWTDEAEAIDRQIRACTPHPGAWTELFAEGPIADNDESTAKSLALHILAAQPADQSNPNTPAELQPGELKVGKKNVWVGTGSTPLELTQVKAQGKKAMRAADWTRGARLSPAACVR
>NZ_CP013673.1|WP_013141141.1|1650332_1651037_+|HAD-family-phosphatase
MKGWPGEPDMDYDVLVADGEAAANAGKPITDVIFDFGNVLIYWDPVAVLIPRYSQKTIDEFLDNDISGFYDVNDLMDGGTSTDEAIAIMRRDKGDKWADILDYYIKNFRDSLTGIVPGARVLVNDLKAAGIGVWGLSNWESSLFHVAEEQCDILQQLDGKLVSGFVKLRKPHKEIYEAALNQFGIKADGALFIDDKAMNIVGSNAAGIRGVRFQDPVKLRELLIANGVNIPAVQ
>NZ_CP013673.1|WP_058101922.1|1647961_1650274_+|primosomal-protein-N'
MTTSGAEQLTLAGLAPRKRRKRAPAEHTPAEQHPIAQVVLDVQALHLGQTFDYFIDEKDSEAAQPGVLVRVRFGSQRVSGVIWARTDTSDTPRSSIRYIERVLSPDVLVPASMREDIGLVAKAYGGTRANILRFAVPPRVAKVETEQRLAASFRRPVGGSLPDNTQGGFAGRGTNPDGTKPAGSTFAVASTVSEGAAQGYRRLTANYADVNVLHDALTGQRFQSFVFDSLPGAQEWQRNMAWMVATALSAGKAAVVELPTMREVEDLMHMLRNYGLKPFAPVPTGGWMGDVAVLNAKTMPAADRYRTYLAVALGQVKVVIGTRAVMYAPVEGPALFAILEDAAYQNMDGMMPYPQARGVMRLRAKSHGGVFVAMANARTPQSQWENTGPGTVETPVSGYSTAIHPLASPLKDATPWVRWLNRDELARLADPSIGARVPHTAVRVLSKALESGPVLLSIPQDNVSETLSCAKCHRQVRCAKCSGPLQLPADRRDSTPRCRWCGAAAINWKCPGCGHERMRVVRVGAAGTAAELAGLFRGVPVVLSSKTQGLVRDVACQPIIVIATPGFEPRVRPVSAEQGSAGHEYRAVAVLDAWTSLYALGVDARLDTLTAWMRAVSLCAPRSRGGQALILGETDPAIAQSLMLWDSRILAAKDLEERVETGMPPAVAAACVWGRRDAVMTLMQRIGALGGDWTACGELPGMLGPVPIAQPDTVDARELEATDDRVKAVIRVPQSRRAELAARLHRETARHVASREPGELRFRVDPKDLI
>NZ_CP013673.1|WP_011068843.1|1647169_1647922_+|phosphoserine-phosphatase-SerB
MSQGFPRIRSMTQEDVHFIDKSAESEVGSPAGSAVSVPTLSEPGLLVMDVDSTLIDEEVIDELGVVAGCGEEIAGVTARAMRGELEFCDALRARVALLEGLPISVFDTVHDKLHFTKGALELIDTLHEHGWKIGVVSGGFHEVVDMLAAEGHIDYWIANRLEVADGCLTGKVLGEIVSKTVKLHALQTWADRLGIPMSQTVAVGDGANDIPMIQAAGLGLAFCAKPKTQLAADKAINDRDLTHVLDYLRR
>NZ_CP013673.1|WP_007055597.1|1646450_1647149_-|DedA-family-protein
MAAATILATDPTPICTTTEPGLIGTITDWLIMLMETIGGIGVALAIALESIFPPIPSEVILPLAGFTAARGTLSLPGAIIWATIGSVLGAWTLYGISRWVGLHRINLAADKIPGVSRKDVSKANDWFTKYGTWSVLIGRVIPVVRSLISIPAGFNRMNFLHFTGWTLLGSAVWNTILVSAGYLLGDQWCSIQGALGVFEDVVIAAVIVIIVWFVVRKVRTVIRNRKSSDGNE
>NZ_CP013673.1|WP_058101923.1|1644824_1646390_-|proteasome-ATPase
MSDTEDLAALNDRLMAKNHALAEALSRAGKELTKAKSQLAQLAQPPLTFATMVKVDSTRTDEDGIQHASAEVISGTRRMVVPVASNVNAARLTAGATVMLNEKLVLVEQRDADTVGQIRSVKQVLDDGRLIVTDASGNPVLIRRSGALAYAGINQGDRIIVDPSVRLAIEALPAEGDKDLVLEETPDVTFADIGGLDSEIGRIRDAVQLPFQHRALFERYDLKPPKGVLLYGPPGNGKTMIAKAVANALCEGGYDTNGDGSISPAETRVKGVFLSVKGPELLNKYVGESERLIRLIFQRARERAADGNPVVVFIDEMDSLLRTRGSGVSSDVETTIVPQFLSELDGVESLDNVMVIGASNRVDMIDPAVLRPGRLDVKIRVGRPKANQAIAIVDHYLTDDLPLEDGVDAHALSAVLVHDIYGASERRHLCDVQEENGQWHALFLADVVSGAMLKNIVDRAKTRAVKESIETGSDVALTVPLLAAAVEDEYRETRDSMADVDPEQWSRINGMDPIRRIRTAE
>NZ_CP013673.1|WP_058101924.1|1643135_1644803_-|proteasome-accessory-factor-PafA2
MTVKRVMGTETEYAVSLNTPDRYNPVQLSFDVVNGAADSHSKSIRWDYRQEDPVNDARGTRLERAAARPDMLTDAPQLNITNVIAPNGGRVYVDHAHPEYSAPETTDPFEAARYDRAGDLIMQAATERARTQTGTPIALHRNNVDGKGSCWGAHENYMMARSVPFDLVTRLMTLHFVTRQIYAGSGRVGIGENSEIPGYQLSQRADYIHVKVGLQTTFERPIINTRDESHSTDEYRRLHVIVGDANRMEVPQALKLGTTSMLLWLLEHADEAGFDLNAFLDELELADPVEAMHTVSHDLTLGASLPLANGGETNAWLIQLKLRQAVYQVAALVEGTDTAGEPAWPDKSTTSIMAMWQQALIDCASIRHTADDDERLAMTGEASRIEWLLKWQLLEKLRRKITAAAAPSVANGWNDPRLKVIDLKWAALDPADSIFTKLEPRTERVMSAADIARAATEPPEDTRAWLRAKLVARFGSEVAAASWSRLTVRDPHAADEGEAVEFYGNAGHMAATDHHLFSLDISDPLAFTKARCETELNSAEHAIDLLKSLAINAER
>NZ_CP013673.1|WP_058102100.1|1667317_1667608_-|CRISPR-associated-endonuclease-Cas2
MMVVVAYDVNTESPEGKRRLRNVAKTCMKYGQRVQNSVFECSVSPSDYLILKHDLAEIMDESQDSLRYYNLGAKYSSKIEHRGRQRHLPIDDVMML
>NZ_CP013673.1|WP_058102099.1|1667693_1668725_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MKQLLNTLYVTSDDAYLSLKNDNVIVQQGDTTLGRIPLRSLEGIMSFSYKGSSPALMGKCSEFGVGLSFFSPHGRYYCSILGEKNRNVLLRREQFRFADDEDAALPFAQSFIIGKIYNCRWVLERTKRDHALRVNSERIAEQSEKLRQALLNARDCTSIDELRGVEGLAAKDYFFAFDDLILRNKDDFFFQQRSRRPPLDRTNALMSFVYSILTSDCIAALQGVGLDPYVGFLHTDRPGRASLALDLVEEFRPVIADRFVLTLINTGAVKPSQFEIRENGGVFLSEGGRKTVLAAWQKRKQETITHPFFNEKIPWGLVPHAQALLLNRAIRGDLDAYPPFMWK
>NZ_CP013673.1|WP_058102098.1|1668721_1669423_-|CRISPR-associated-protein-Cas4
MKEPTDYPEDDWLALSGLQHFAFCRRQWALIHIEQQWEDNYLTTAGSLEHDRAHDYSESETRGSLLIMRDLRVFSRRLGITGACDVVEFRQSEAGVPLHGRSGTWLPYPVEYKHGAPKQTDADRLQLCAEAMCLEEMLACAIPEGALFYQQTRHRERVSFDESLRNRIVTMTGEMHDLFARGHTPKVRPSKACRACSLRDVCLPKLVRTRSARQFIEEAVRGEVEIGEKSDHI
>NZ_CP013673.1|WP_014484099.1|1669461_1670313_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTSLQHKIDFVLTFAVENANPNGDPLNGNRPRTTAEGLGEMSDVAEKRKIRNRLQDAGERIFVQSTDRTDDGEKSLSDRWKAFTKTLSKEDQKDREALSYRACEQWIDVRSFGQVFAFKGKEKEGDASVSIPVRGPFTIQSAFSLEPIAIDDVQITKSVNGETTDTNKKSSDTMGMKHRVSGRAVYVTHGSISPQLAEKTGFTEKDAEKIKEALLTLFENDESSARPAGSMEVVNLAWFTHNSKAGQYSSAKVHRTAKVDEEGVITVDTTHIPGLHYEVLEGR
>NZ_CP013673.1|WP_058102097.1|1670316_1672275_-|CRISPR-associated-protein-Cas8
MSLWSSLLQTYDAVNSSAGITPLNEDVNKTLLPLYHTTLKTQLQVTLDENGYPTIKRDNADIEIIAPCTEQSMGRSGKVLPPHPLFDQLQYIDTNYDPVKHESYLSQLASWKGDNAKLNAIYQYLSQHSVIEEARAQGIGIDPKKDSKIGVRFAVHVRHGDYEPKVWADHAIRDLWIAHEEQVRHGASLGTDLFGETLYKPSTNFPKKIVNVNGNAKLISANDNTYFTFRGRFANRDEALSIDTLTSQKIHTTLRWLATNNGTLTGSQDIVIWAIDGHPTDNVLDPTGNSRDVAEQVDDRTDSEKLIDANVQTYANYAKQFGKLLRGYGNEKVLQQMQQHSRRIVVAIFDAATSGRLSVTFYRELFQNEYIESVLQWHEDAAWYLTCFDNKNSASTDDEAPRGSKKSSDKPKPIPYIGAPSFADVINCVYSTDDHSSDSYRRFAKYVKKQLVECMFSNAGLPASLLQPAFHKVIRPLSYDSLSVWQHDFEVACSMWKKYYIDQDKKIPLDERNNITMDLDEKRTDRDYLFGQLLALADNYEYRVLLRQSGGRTPDRTTNAVKLMNNFVAKPSTTWLTLRQQLNPYIISSTNGMFFQNEVDEVMSKFKEGDFESNKPLSSLFLLGYSHKRRQLIQRADAAKQLKEQNIENKGE
>NZ_CP013673.1|WP_058102102.1|1672277_1672982_-|type-I-C-CRISPR-associated-protein-Cas5
MEKHRNSIEYVIYGDYALFSEVATRTGGEKNSYQIPTYQALKGITESIYWKPTIVWVIDAVRVMNKIQTEGKGIRPIKMSGGNDLSYYTYLKKVKYQVLAHFEWNEQREDLRVDRNENKHHNIAKRSVNLGGRRDIFLGTRECQGYVEPCEFGSGEGFYDGYGDWQFGFEFHSFIYPDENPEHDFIAQFWRPIMHDGIIQFERPDSTQLDQRIIRRNQHVKDFIEGCNFSMAEE
>NZ_CP013673.1|WP_058102096.1|1672988_1675427_-|CRISPR-associated-helicase/endonuclease-Cas3
MGQALMPKDLLLARKDDDGNTQTLYDHLHNTAELAAGFEKRSSVTAFAAGLLHDSGKATDDFKRYLLTGNRKRGEVVHAKQGAFIVDDCAADFPSSAASMITAEVLELAIANHHGHLPDCLDACGGTAYFRKLTGENKKAEQYHYQEVLSHVSSLNLDINTNFANSVVETNRLLEIVDSCGISPRNTRNSRSFFLGLYAKYIYSRLVDADRVDAANFTAHQPYTSQTPNWEELTRRLENAISGFDTSSKISKIRMRISENCLAASTRDTGIYRLGVPTGGGKTLASLRFALHHAQETGKHHIIYITPYLSITEQTVQVFRNVLDLDKDDEILLEHYSSVVPDKDDEKEQQRRLAAERWDKPIIVTTMVQFLETVMSAKATRLRKFHNLADSVIVFDEVQALPTNTINVFNEVVSFLSKILGSTILLCSATQPLLEQTDRRNLLLSDKPDLIDPDNDYAEQLRRTNIVASSQGLTLDDFAAEIYSKALDNGNCLAVVNLKGEAKQLYQLVKELDVDHRFTLVHLSTAMCGAHRKNQLAVLKKCLPKKTGDSGQPVICISTQLIEAGVDISFSCVIRAMAGLDSILQAAGRCNRNGESQMPRNVYVYSIKDESGLRYLPEIQLGKEITDQLIHDYPEQDLLSAFMIEEYYRAFLIRYPKLVDSKSRNIGTMDYSILGGEETVYDLLSFNRRRRGLYCNRVGEQYPYAFAQAFQTVGDSFHVIPGGTTDVVVHYGQAMELIDQLNGEGDFASKIKILGSLQEYTVSLFDYEFKALDKSKSISEANGDFGILVLNEENYSQDFGFLLKAEMPLLMK
>NZ_CP013673.1|WP_116868976.1|1676105_1676327_-|transposase
MEEFSRLGEKIDRRRFDILRTIRSGLSNARLEAVNNKIKTTIKIGYGYRNLGNLIALVMLRCGGLNLQLPGRQ
>NZ_CP013673.1|WP_058102094.1|1677049_1680361_-|mupirocin-resistant-isoleucine--tRNA-ligase
MSENVYPKANEGGETAHVAPNPSFPDMEETVLDYWDKDDTFQKSVERNPSGDHSQNEFVFFDGPPFANGLPHYGHLLTGYAKDVIPRYQTMKGRKVNRVFGWDTHGLPAELEAQKELGIDSVDQIEKMGIDKFNDACRASVLKYTNEWQNYVHRQARWVDFEHGYKTLNIPYMESVMWAFKQLYDKGLAYQGYRVLPYCPKDRTPLSAHELRMDADVYQDRQDTTVSVAVKMRDEDDAYAVFWTTTPWTVPTNFAIVVGADIDYVEVRPTEGKFAGKKFYLGKDLLPHYEKELGENYEVVRELKGSELEGRRYYPVFPYFAGETAESEGHVPGPNGYTIFTADYVDTVEGTGLVHQAPYGEDDMNTLNAKGIKSTDVLDDGCRFTAQCPDYEGDFVFDANLPILRNLRAGDGPLASIPEERRAILFQEKSYVHSYPHCWRCATPLIYKPVSSWFVSVTKIKPRLLELNQQINWIPGNVKDGQFGKWLANARDWSISRNRFWGSPIPVWVSDDPKYPRVDVYGSLEELKADFGDYPRDKDGNINMHRPWIDNLVRVNPDDPTGKSHMHRISDVLDCWFESGSMSFAQFHYPFENKEKFEQHFPADYIVEYIGQTRGWFYLLHVMATALFDRPAFKNVICHGIVLGSDGQKMSKHLRNYPDVNGVFDKYGSDAMRWFLMSSPILRGGNLIVTADGIRDTVRQVMLPVWSSYYFFTLYANAANGGAGFDARQLRADEVAGLPEMDRYLLARTRRLVLAAEKSLNEFAISDACDAVSDFIDVLTNWYIRNTRDRFWNEDASAFNTLYTVLEAFMRVLAPLAPMEAESVWRGLTGGESVHLADWPFVVDEKTGEDTELGRVLVDDPALVDAMEKVREVVSGTLSLRKAAKIRVRQPLSKLTVVVENVDAVKAYDELLKAELNIKNIEFSTLEDASAHGLKIVHELRVNARAAGPRLGKQVQFAIKASKSGDWHVDAASGAPVVSTPSGDLALVEGEYELINRVEEENATEAAASVSAALPTGGFVILDTALDADLLAEGYARDVIRSVQDARKAADLDIADRISLALTVPADDVAKVEQFRDLIAHETLASSFEVKEGAELGVEVAKA
>NZ_CP013673.1|WP_013410712.1|1680954_1682166_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MTYDFTSIMDRHGKDAIAVDGLGTDLGFAPDPPRDGFDVIPMWVADMNFPTVPTVPQAIIERAQHPVYGYFSPTDDYYNSIIDWQSTRNGVTGLTSEAIGYENGVLGGVISTLTAFAAPGDSVLLHSPTYIGFTMCIENNGYRIVHSPLKLDEHGVWRMDYEDMDKKLKEHHIHVAVFCSPHNPCGRVWERWEIEKAMEVYKANDCVVISDEIWSDLTLGNHQHIPTQSVSEDARNRTAAFYAPSKTFNLAGLVGSYHIIYNPMLRDRIVAKGSKSHYNEMNVLSMHALIGAYKPEGHEWLDELKEVLTGNVDYAYDYITKHFQGVSLAKPEGTYMLLLDCEQWCKAHGLTLAELEKRGWDVGVDWQDGSMFQAPYSIRVNLALPLSRIKEAMRRLDQYVFNA

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Crispr_ID: NZ_CP013673_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013673_6

1892256-1892341

Orphan

Consensus_repeat	Method
GGCCCTGAGCGTGCGGGCGCGGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013673_6

>merge|NZ_CP013673|6|1892256-1892341|CRISPRCasFinder
GGCCCTGAGCGTGCGGGCGCGGAATCGCATTTGAAGCGGCATTGCCGCCATTGGCACCGGCGCCGCCCTGAGCGTGCGGGCGCGGA

>NZ_CP013673|6|6|1892256-1892341|CRISPRCasFinder
GGCCCTGAGCGTGCGGGCGCGGA	ATCGCATTTGAAGCGGCATTGCCGCCATTGGCACCGGCGC
CGCCCTGAGCGTGCGGGCGCGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013673.1\|WP_007056648.1\|1897932_1898334_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226064
NZ_CP013673.1\|WP_077382808.1\|1894328_1895150_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_081040199.1\|1902298_1902610_+\|ATPase	unknown	unknown	unknown
NZ_CP013673.1\|WP_007053813.1\|1893146_1894214_-\|transcription-termination/antitermination-protein-NusA	unknown	unknown	gnl\|CDD\|237061
NZ_CP013673.1\|WP_007053815.1\|1888160_1889324_-\|tRNA-pseudouridine(55)-synthase-TruB	unknown	unknown	gnl\|CDD\|235113
NZ_CP013673.1\|WP_011068749.1\|1884625_1885204_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007053811.1\|1895190_1896234_-\|LacI-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_CP013673.1\|WP_007055304.1\|1899143_1899944_-\|transglutaminase-family-protein	unknown	unknown	gnl\|CDD\|224224
NZ_CP013673.1\|WP_004268639.1\|1884344_1884434_-\|AURKAIP1/COX24-domain-containing-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007053052.1\|1900150_1902331_-\|circularly-permuted-type-2-ATP-grasp-protein	unknown	unknown	gnl\|CDD\|379601
NZ_CP013673.1\|WP_007052308.1\|1889325_1889799_-\|30S-ribosome-binding-factor-RbfA	unknown	unknown	gnl\|CDD\|234787
NZ_CP013673.1\|WP_007055359.1\|1885385_1886924_+\|DNA-repair-protein-RadA	unknown	unknown	gnl\|CDD\|236994
NZ_CP013673.1\|WP_007053049.1\|1903599_1904142_-\|50S-ribosomal-protein-L17	unknown	unknown	gnl\|CDD\|235522
NZ_CP013673.1\|WP_081040198.1\|1896766_1897933_-\|alpha-L-arabinofuranosidase	unknown	unknown	gnl\|CDD\|226064
NZ_CP013673.1\|WP_032682752.1\|1902606_1903518_+\|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl\|CDD\|211337
NZ_CP013673.1\|WP_011068752.1\|1882026_1882374_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013673.1\|WP_007056729.1\|1883493_1884192_+\|ribose-5-phosphate-isomerase-RpiA	unknown	unknown	gnl\|CDD\|234816
NZ_CP013673.1\|WP_058061029.1\|1880223_1881840_+\|pyridine-nucleotide-disulfide-oxidoreductase	unknown	unknown	gnl\|CDD\|235798
NZ_CP013673.1\|WP_075662791.1\|1882376_1883363_+\|ribonuclease-HI	unknown	unknown	gnl\|CDD\|260010
NZ_CP013673.1\|WP_007055364.1\|1886938_1888063_-\|FAD-synthase	unknown	unknown	gnl\|CDD\|235536

Protein	Function_ID	Function_description	E-value
NZ_CP013673.1\|WP_007056648.1\|1897932_1898334_-\|hypothetical-protein	gnl\|CDD\|226064	COG3534, AbfA, Alpha-L-arabinofuranosidase [Carbohydrate transport and metabolism].	4.0158e-59
NZ_CP013673.1\|WP_007053811.1\|1895190_1896234_-\|LacI-family-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.46775e-80
NZ_CP013673.1\|WP_007053813.1\|1893146_1894214_-\|transcription-termination/antitermination-protein-NusA	gnl\|CDD\|237061	PRK12327, nusA, transcription elongation factor NusA; Provisional.	2.23491e-150
NZ_CP013673.1\|WP_007053815.1\|1888160_1889324_-\|tRNA-pseudouridine(55)-synthase-TruB	gnl\|CDD\|235113	PRK03287, truB, tRNA pseudouridine synthase B; Provisional.	6.2196e-102
NZ_CP013673.1\|WP_007055304.1\|1899143_1899944_-\|transglutaminase-family-protein	gnl\|CDD\|224224	COG1305, COG1305, Transglutaminase-like enzymes, putative cysteine proteases [Amino acid transport and metabolism].	3.46877e-29
NZ_CP013673.1\|WP_007053052.1\|1900150_1902331_-\|circularly-permuted-type-2-ATP-grasp-protein	gnl\|CDD\|379601	pfam14403, CP_ATPgrasp_2, Circularly permuted ATP-grasp type 2. Circularly permuted ATP-grasp prototyped by Roseiflexus RoseRS_2616 that is associated in gene neighborhoods with a GCS2-like COOH-NH2 ligase, alpha/beta hydrolase fold peptidase, GAT-II -like amidohydrolase, and M20 peptidase. Members of this family are predicted to be involved in the biosynthesis of small peptides.	0
NZ_CP013673.1\|WP_007052308.1\|1889325_1889799_-\|30S-ribosome-binding-factor-RbfA	gnl\|CDD\|234787	PRK00521, rbfA, 30S ribosome-binding factor RbfA.	1.2318e-44
NZ_CP013673.1\|WP_007055359.1\|1885385_1886924_+\|DNA-repair-protein-RadA	gnl\|CDD\|236994	PRK11823, PRK11823, DNA repair protein RadA; Provisional.	0
NZ_CP013673.1\|WP_007053049.1\|1903599_1904142_-\|50S-ribosomal-protein-L17	gnl\|CDD\|235522	PRK05591, rplQ, 50S ribosomal protein L17; Validated.	1.51666e-56
NZ_CP013673.1\|WP_081040198.1\|1896766_1897933_-\|alpha-L-arabinofuranosidase	gnl\|CDD\|226064	COG3534, AbfA, Alpha-L-arabinofuranosidase [Carbohydrate transport and metabolism].	1.94944e-117
NZ_CP013673.1\|WP_032682752.1\|1902606_1903518_+\|tRNA-pseudouridine(38-40)-synthase-TruA	gnl\|CDD\|211337	cd02570, PseudoU_synth_EcTruA, Eukaryotic and bacterial pseudouridine synthases similar to E. coli TruA. This group consists of eukaryotic and bacterial pseudouridine synthases similar to E. coli TruA, Pseudomonas aeruginosa truA and human pseudouridine synthase-like 1 (PUSL1). Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil, psi). No cofactors are required. E. coli TruA makes psi38/39 and/or 40 in tRNA. psi38 and psi39 in tRNAs are highly phylogenetically conserved. P. aeruginosa truA is required for induction of type III secretory genes and may act through modifying tRNAs critical for the expression of type III genes or their regulators.	1.01702e-94
NZ_CP013673.1\|WP_007056729.1\|1883493_1884192_+\|ribose-5-phosphate-isomerase-RpiA	gnl\|CDD\|234816	PRK00702, PRK00702, ribose-5-phosphate isomerase RpiA.	6.02536e-120
NZ_CP013673.1\|WP_058061029.1\|1880223_1881840_+\|pyridine-nucleotide-disulfide-oxidoreductase	gnl\|CDD\|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	1.88719e-82
NZ_CP013673.1\|WP_075662791.1\|1882376_1883363_+\|ribonuclease-HI	gnl\|CDD\|260010	cd09278, RNase_HI_prokaryote_like, RNase HI family found mainly in prokaryotes. Ribonuclease H (RNase H) is classified into two evolutionarily unrelated families, type 1 (prokaryotic RNase HI, eukaryotic RNase H1 and viral RNase H) and type 2 (prokaryotic RNase HII and HIII, and eukaryotic RNase H2). RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner. RNase H is involved in DNA replication, repair and transcription. RNase H is widely present in various organisms, including bacteria, archaea and eukaryotes and most prokaryotic and eukaryotic genomes contain multiple RNase H genes. Despite the lack of amino acid sequence homology, type 1 and type 2 RNase H share a main-chain fold and steric configurations of the four acidic active-site (DEDD), residues and have the same catalytic mechanism and functions in cells. One of the important functions of RNase H is to remove Okazaki fragments during DNA replication. Prokaryotic RNase H varies greatly in domain structures and substrate specificities. Prokaryotes and some single-cell eukaryotes do not require RNase H for viability.	5.67618e-62
NZ_CP013673.1\|WP_007055364.1\|1886938_1888063_-\|FAD-synthase	gnl\|CDD\|235536	PRK05627, PRK05627, bifunctional riboflavin kinase/FAD synthetase.	5.18065e-81

>NZ_CP013673.1|WP_007052308.1|1889325_1889799_-|30S-ribosome-binding-factor-RbfA
MAGTNPRAARIAALIQRVVASSIERELHDKRLASITVTEVRVTNDLQIAKVYWTQLGHEGHEEGERKRAQQALDQAKGHLRSLVGHKAGLRLTPQLQFVFDEVPGEAHEIEDILAVAKKRDEELARARATAQYAGDADPYKHDDEPSDDFEDDSDEE
>NZ_CP013673.1|WP_007053815.1|1888160_1889324_-|tRNA-pseudouridine(55)-synthase-TruB
MLHTTPSGLLIIDKPQGVTSFDAVAAVRGALHIKKVGHAGTLDPMATGTLVIAFGHATRLLNAIVAHDKTYEATIRLGLRTTTDDAEGEVLVDDEARSRWQTLSAQLTEGGQSGEPTALPTASWQDLLTRTIATNFTGDIEQVPNTFSAIKINGQRAYDLAREGKDVELKPRPVTISEFTVLDIRSGFVAGEQTAEPLREDANTGAIPALDVDVRISCSSGTYIRALARDLGKELGVGGYLTRLRRTRVGRFALPDDASGLIAPEAMLDTRTHTVTAHTDQKTFTNREGQTVTRNKCVLDTPEGLAGDERRNWLLDHALTMEQAARGAMPALDITPEEASELRFGRRIERTISEPTAAIVPQTHDVAAIIERANAHQAKPVTVFPLA
>NZ_CP013673.1|WP_007055364.1|1886938_1888063_-|FAD-synthase
MDITHLTPDAEGSIEWPSFSNDKKAVVTLGAFDGMHLGHQAVIKRVVELAHQHDAFSVVILFDPRPAFVHGWVISHHGEEPAVQNVDAEALTSVDDRLHRMEQFGVDHVLVVHYTLAFAAMSYIFFLGRLTGKLGMRTLVLGQDAAMGKGREGDVKHIANLAAATGVFELDVVDDRGPGEVRIPRDFKPEAPSEWGEPVDPLANATKAERRAWSKKNQAKAMRAWSSTNVRYLLAHGRIQDANAILGAPHSIEGEVVHGEERGRTIGFPTANLGSDIAGYIPVDGVYAGWLVDGENRWPAAISIGTKPTFSEKTGLNERVVEAYCITEEWIDLYDHKVRVEFVGFLRPQVKFDGPDQLVDELKRNVEETKRLTA
>NZ_CP013673.1|WP_007055359.1|1885385_1886924_+|DNA-repair-protein-RadA
MAKSSVQYVCSECGWNGPKWYGRCPECGQWGTVEEFHEARPAAGSRTAAPGRTSRTQSVTVANNARSAARPITEVGTESVERLGTGFSEFDRVLGGGVVPGSVTLIAGEPGIGKSTLLLQTAGNIARVVAGDSTFRGAGQRSAQQSGRAQGNASNTVPMRGNASSTHANTVLYISGEESQAQVRLRASRINAVEPNLLLASTTDLSTVLGLIEQNKPALAIVDSAQTIVSQEVDGISGGSTQVREVASALIDTAKTLDIPVFLVGHVTKDGSIAGPRTLEHLVDVVCQFEGDSETALRMLRAVKNRFGPTDEVGCFDMSGEGIEEVTDPAGLFLSGDGPDAANAAPVEGTCVTFTLDGHRSLPIEVQALVTTSVLPTPRRAVNGVDPSRIAMLVAVLYRHSKLNLLSNDLYISTIAGGQAKEPGSDLAIVAALASAATSKPIARATCAIGEISLTGQVRPVPRMEYRLREAARLGFTTAVIPPLRKPVHVEGLQLVESNTLSDALDALGVRK
>NZ_CP013673.1|WP_011068749.1|1884625_1885204_-|hypothetical-protein
MVVAAAVVIILAVLSAFVWPGWAIQKNDGTSTTTQNSQQKTESSEPTKPTIDATALPDDASELLKAMPGSVLNYARTKADASTTWNSASPLEEYTLTYSTGDAAKDVTLVAAQWSSADNAKTQYDALVAAQTGDESASGNVKVSGNVTGAYVVKADASNSKNAVAIWQNDTVVFQATGTKEAVDRFYQKFPM
>NZ_CP013673.1|WP_004268639.1|1884344_1884434_-|AURKAIP1/COX24-domain-containing-protein
MGSVIKKRRKRMSKKKHRKLLRKTRHQRK
>NZ_CP013673.1|WP_007056729.1|1883493_1884192_+|ribose-5-phosphate-isomerase-RpiA
MDKAQQDALKKAAGIEAAKLVENGMIAGLGTGSTVKFLVDELGRRHQEEGLEFTGVTTSRRTQVQAESYGIKIVDIDDVDHIDVTIDGADEVDKNFNGIKGGGAALLWEKIVATNSNQIVWIVDESKVVDTIGKFPLPVEVIPFGAGQVIKKFEARGYKPVLRLDADGKEVRTDENNFVVDLHLERIDHPQELAEDLINTVGVVEHGLFLNMVDKVIVGDPNGPRVMTNANK
>NZ_CP013673.1|WP_075662791.1|1882376_1883363_+|ribonuclease-HI
MMLFTLFTTLFCLALGNPTSARDCTACVRVENMTITVSTDGSALGNPNGPMGWAWADHEQNAGGKPGHKHDDHGYDAGGATNGTNQIGELCAVLEALRAHPGPEPLLIESDSQYAINCSTKWVKGWKKNGWKNSQKKPVKNKELIQAIDREISQRPGPVDFRWVKGHAGNEGNELVDELARTYAGDCRSGARDGYLPIEGWQSLLGSEYAHGTDVPPDVQLVLDGKADAASLRKPAAATDQTDAARPETKSSSPLAAQSTQPVQSTQPVPPAKPSGLTVSGTLTFSPAPKTSPYFNGQPMPIKGSIEIEGYVDGDGNLTITNAPFVRH
>NZ_CP013673.1|WP_011068752.1|1882026_1882374_+|hypothetical-protein
MSEASNPKRRRMNQPRPSGRPGAKAMPPGPSATVLELPAISMVPLDAAVEVEPSLSASGLRISMLPSLVLYSPLFSFQIPDAPLLPASPAERKCLVFLVSAHLFTRDGMFFKQSQ
>NZ_CP013673.1|WP_058061029.1|1880223_1881840_+|pyridine-nucleotide-disulfide-oxidoreductase
MSISTPNAISTPNTSPTITTDALIIGFGKGGKTLAAKLSAAGRKVVVAEASADMYGGTCINIGCLPSKSLILSAEQARRDGANSTPETREAAFEAAIKEKRRVTSMLRDKNYHKLADQDNITVITGRAHFTGPHSVEIATAEGPVAVTASKIFINTGATPRIPDIPGIHTTPGVYTSTGLMDLDDMPQRLVIIGSGFIGLEFASMFADFGTAVTVLQHNAEFLPREDADVAAAIRAQLEAQGVKFLFNADTKAIAPAADGGVRLSVAVKGMTRGASQACDSTPAGTGNAHTDITGATDTTTTTSPTSNPTDHATMSHVQTKPSDDGEPRFAEPAEARFCLTTDAVLVATGRTPNVEGLHLEAAGVELTERGAVKVDELLRTTAADIWALGDVNGGPQHTYISLDDYRVVWSQLNGSDRPHTVKDRKHVPSSTFLATPYSRVGLNEREAKAAGLDYVVKRLPVAAVPKAQVMRRPDGLMKAIVERNTGRILGAMLLSVESHEVINIVKLAMDLDAPASTLRDMVFTHPTIAEALNDLFA
>NZ_CP013673.1|WP_007053813.1|1893146_1894214_-|transcription-termination/antitermination-protein-NusA
MELDLTGIHKLAAEQGIDPETLDDALAEALRLAYLKTPHAAKHARVELDERSGNFTVWAADEIPVEPTEDNPYPVPKLGEEYDDTPRDFGRLAAATARQVITQLFRRAEDEKVFGAFSGQKGKLITGIIQQDASDPSNVHVAMGDVEAILPRREQVPGERYRHGERIRVYVVNVARGIKGPEIVVSRSHPELVRKLFEREVPELVSGAVSIMAIAREAGARTKIAVKANTDGVNPKGALIGPGGARVRAVMENLGPEKIDIVDYSDDPAKFVAAALSPAVATGVQVISEKNKTAIAFIHDDQLSLAIGKEGQNARLAAKLTGWKIGIESAEAHAKKVAAEKAAQAAAEAAAPEAE
>NZ_CP013673.1|WP_077382808.1|1894328_1895150_+|hypothetical-protein
MASVLCASAMLCSLSACSMPRLAGRAEAEAQMTPCEKAMTLAGYATHPAEGTPLLEQYATGLAAPLAWIDVAGYCSGRFAEGTLRDAQTKQWLAFLADKFGQSAPEVTPARLDGVTSANVDRSVLDAMAVAEDRAGFAIEVLAARGQTAGATLALSDMHKTAGQQLVALANGNFDDSGAQSSSSGQNDPRQKVYAIDQLLANPTTIADKASGQTVPTAAAIEMDCARAQIKAVTESKSSTESDTLLILAALAAKHAYTAFQLGYPATDAALFE
>NZ_CP013673.1|WP_007053811.1|1895190_1896234_-|LacI-family-transcriptional-regulator
MGNRVTIKDVAREANVSIKTVSNVLNDTGSMRPDTRRRVEEVMRKLGYTVNISARAMRSGGTKLIGLNIFDFSQPFVPFFTDKVIEYAKERHYGVVINTYGSDGEGLVASVDESYRLGAEGWILFVMSPLADEGAVLEQPYPIVTTGDHLAYGKSDWITMPNIESISTVVGRFLDEGAQTVALMGVLPELVDEAVLRRQTEGTQALRAQGYVKAFEERGLSVNWRYVIPAESMNQREGMRVTKAMLDKLPCPDVVVCLNDAIALGAIHELQRCGLHVPDDVQVVGFDNVPEAEYSVPALTTIDPHIDDYAKHAVDMLIDRIEGYSGPARTYTTDFTLVERASTRLAH
>NZ_CP013673.1|WP_081040198.1|1896766_1897933_-|alpha-L-arabinofuranosidase
MEAVNLGTRGLEEALDLLEYANIPGGTKLSEERRANGADQPFGIKMWCLGNEMDGPWQTGHKSAEDYGTLAASVAAGMRAIDPNVELVVCGSSSHVMDTFGKWEETVLEKTFDNVNFVSCHAYYHPELQPDGTRDMKSFLASGVDMDGFINDVAAAIDATKARLKSKHDVFISFDEWNVWYLNEEPSKNPEGIGNWPVAPRLLEDVYSAADAVVFGDLMITLLKNADRVHAASLAQLVNVIAPIMTEPGGPTWRQTTFYPFSLTAKLAKGGTVLEPKLASGTYETDKYGEVPTINSVAVRGEDGTISVFVVNRSMEAANDFAIKLPEGFALSAVEAQTLHEDDLLAKNTLEDQNRVVLHPNTTITSDADTGTVRVTLPPVSWTAVHVK
>NZ_CP013673.1|WP_007056648.1|1897932_1898334_-|hypothetical-protein
MSEHSHDNKPGELEESRLVVDNDFEVAPVNDRLFGSFVEHLGRCVYDGIYEPGHPEADEDGFRKDVIELVKELGATTIRYPGGNFVSGYRWEDGVGPRDERPRRLDLAWHSTETNQFGLHEMAKWLEKPAATS
>NZ_CP013673.1|WP_007055304.1|1899143_1899944_-|transglutaminase-family-protein
MKKLVFDYEMRLSFSAPVTDHRFQLRCIPSTGPRQQVIDVEVKIQPETELETTIDSFDSVVMTGFIPEPHDIFSYSVTGIAFVDNAHIHKEAYKPLYRFNSALTIPGPNVEAMIAVCRERLAALPSDATPVQQAAEVMDEVYKAFVYTPGSTTIRTTAEQALAQRKGVCQDYAHVMLSVCRHVGLTARYIAGLLGGEGATHAWVEVYQDGRWVGLDPTHNRLVDDSYITIAHGRDYRDCMLDIGIFSGYNVQQSQWVNASVHEQVA
>NZ_CP013673.1|WP_007053052.1|1900150_1902331_-|circularly-permuted-type-2-ATP-grasp-protein
MIESAARRLAHELVNRREAINRELSRNGVRFGIYKNGEYHDRLFPYDPVPRIIESDEYDELEKGLKQRVNALNAYLKDIYSDKAIIHDGVVPEEYVYTSAGYFPQVNGVTPPGGIFAHIAGEDLVQGEDGRWWVLEDNLRIPSGASYPLFVRDIERRISPRLFRDVRIRDNREYPRLLRKAMDFVSTEGIAVVLTPGRYNSAFFEHAYLAEKTGAALAFPEDLEVVDNKVYFLDYAGKRHRVGVVYRRLSDEFLDPFAFNPDSVIGVPGILSAYRAGNVAIVNAPGNGAADDKAIYYFVPQMIKYYLGEEPILNNAPTYMPMFEADRKEVLNRMGELVIKDVAEAGGYGVVFGSSLDAAAREELANRIKEEPRRFIAQEVIQFRDIDVVDPKTGEMSPRKCDLRAFVVTGKNTHVWYSGLTRYSSVPGQMIVNSSQGGGFKDTWVLAPESGVEHEYGAETQVVNLLNQSRRHSLSLVTASKADNLYWLGRYTERAFTTLNQFFPFYDRVMDTDVDAFRPFAHALDLPEDFEDFDGFVNSFLYDGSNPDSVRSAVTSAFNNAVILRPELSSRLLQYVELAMTNITDAAKYAADAEDIYKQRDITDDMLAFWGGIENSPVDPTLKAFIFIGKYLERIDLYTRFGLTMEELEAPLKKLAAYSMTLDGMPLPSCFADGLSWLVGQLPSRGYQEVADLLKKYLDDYSGRVSALAIKDMGSLSSMNMDAKRP
>NZ_CP013673.1|WP_081040199.1|1902298_1902610_+|ATPase
MGQSACCGFDHRACSLLWRLLWLQAVRRVERTLTPQAVTGFDGFNLRRARFNKRARMLQAGHFAGRVHLDDRTRLADRTHLADRTHLADRTHLADHTRYNEWL
>NZ_CP013673.1|WP_032682752.1|1902606_1903518_+|tRNA-pseudouridine(38-40)-synthase-TruA
MTRLRIDLAYDGGGFYGWAKQPNLRTVQGTIEDALHKVLRVPADDAAEPLRLTVAGRTDTGVHASHQVAHLDVSDEVLNRCVGHMTIPVTEALTRRLKAVLPPDIVIHGIAVAPVGFDARFSALERTYVYRVADRSSEVDPRLRGCVLTVDEALDLELMNRAASLTIGLHDFGSFATPNPGGTTIREVKTAYWRRVPITPLVPDEMASHEAYRTPSLESGLVVFTIVADAFARNMVRSLVGSCIKVGSGRKSLEWFAGKMAEPVREGSSGPIAPQGLTLEHIAYPADDQLAARAEAIRAVRTL
>NZ_CP013673.1|WP_007053049.1|1903599_1904142_-|50S-ribosomal-protein-L17
MPTPKKGPRLASSPAHERLMLANMATSLFQNGRITTTLPKAKRLRPLAERLITFAKRGDLHSRRRVMRVIRNKSVVHILFTQIAEQMEQREGGYTRIVKIAPRVGDAAPAAVIELVTEPVAKKAVVKEAEAAAKVAEEEAPAVEAEATEAAEAVEAPVEETAAAEAEAPAEEAADAEKAE

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP013673_5	5.163\|1666865\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666865-1666899	35	NZ_CP013673.1	1858358-1858392	0	1.0

1. spacer 5.163|1666865|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to position: 1858358-1858392, mismatch: 0, identity: 1.0

cgcaacaatgcgatcagcgacgagtacccggaagg	CRISPR spacer
cgcaacaatgcgatcagcgacgagtacccggaagg	Protospacer
***********************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP013673_5	5.15\|1657064\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657064-1657096	33	NZ_KM406416	Bifidobacterium breve strain JCM 7017 plasmid megaplasmid pMP7017, complete sequence	100844-100876	0	1.0
NZ_CP013673_5	5.125\|1664341\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664341-1664376	36	NC_010930	Bifidobacterium breve plasmid pB21a, complete sequence	743-778	0	1.0
NZ_CP013673_5	5.160\|1666667\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666667-1666700	34	MH444512	Bifidobacterium phage Willi, complete genome	28161-28194	0	1.0
NZ_CP013673_5	5.160\|1666667\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666667-1666700	34	MK932884	Bifidobacterium phage PMBT6, complete genome	28161-28194	0	1.0
NZ_CP013673_5	5.33\|1658257\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658257-1658291	35	MK415409	Phage YS1-2_2434, complete genome	26327-26361	1	0.971
NZ_CP013673_5	5.58\|1659911\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659911-1659942	32	MK415409	Phage YS1-2_2434, complete genome	8352-8383	1	0.969
NZ_CP013673_1	1.5\|171771\|24\|NZ_CP013673\|CRISPRCasFinder	171771-171794	24	NZ_CP047177	Rathayibacter sp. VKM Ac-2759 plasmid unnamed1, complete sequence	98015-98038	3	0.875
NZ_CP013673_5	5.133\|1664871\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664871-1664905	35	MN856058	Myoviridae sp. isolate 283, complete genome	6297-6331	3	0.914
NZ_CP013673_5	5.133\|1664871\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664871-1664905	35	MT006237	Bifidobacterium phage BigBern1, complete genome	33615-33649	3	0.914
NZ_CP013673_1	1.5\|171771\|24\|NZ_CP013673\|CRISPRCasFinder	171771-171794	24	NZ_CP013110	Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence	1789555-1789578	4	0.833
NZ_CP013673_5	5.4\|1656332\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1656332-1656365	34	MK415409	Phage YS1-2_2434, complete genome	19788-19821	4	0.882
NZ_CP013673_5	5.8\|1656598\|37\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1656598-1656634	37	MK415409	Phage YS1-2_2434, complete genome	16917-16953	4	0.892
NZ_CP013673_5	5.42\|1658854\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658854-1658888	35	MK415409	Phage YS1-2_2434, complete genome	19387-19421	4	0.886
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NC_010625	Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence	1569575-1569607	6	0.818
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	NZ_CP025811	Sulfitobacter sp. SK025 plasmid unnamed3, complete sequence	51303-51335	7	0.788
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	NZ_CP015738	Shinella sp. HZN7 plasmid pShin-02, complete sequence	383111-383143	7	0.788
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP035092	Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence	562347-562379	7	0.788
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_008688	Paracoccus denitrificans PD1222 plasmid 1, complete sequence	155880-155912	7	0.788
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	527817-527849	7	0.788
NZ_CP013673_5	5.19\|1657328\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657328-1657361	34	KX683428	Mycobacterium phage TBond007, complete genome	15976-16009	8	0.765
NZ_CP013673_5	5.19\|1657328\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657328-1657361	34	NC_042325	Mycobacterium virus Pixie, complete genome	15977-16010	8	0.765
NZ_CP013673_5	5.36\|1658456\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658456-1658489	34	MG962374	Mycobacterium phage Paola, complete genome	27448-27481	8	0.765
NZ_CP013673_5	5.36\|1658456\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658456-1658489	34	MH051255	Mycobacterium phage Leston, complete genome	27578-27611	8	0.765
NZ_CP013673_5	5.36\|1658456\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658456-1658489	34	MF185720	Mycobacterium phage Guillsminger, complete genome	27448-27481	8	0.765
NZ_CP013673_5	5.39\|1658656\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658656-1658689	34	NZ_CP025613	Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence	550760-550793	8	0.765
NZ_CP013673_5	5.40\|1658722\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658722-1658755	34	NZ_CP025613	Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence	550760-550793	8	0.765
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	MN694293	Marine virus AFVG_250M335, complete genome	1301-1333	8	0.758
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	NC_009427	Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence	158740-158772	8	0.758
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	NZ_CP039697	Novosphingobium sp. ABRDHK2 plasmid pABRDHK22, complete sequence	146255-146287	8	0.758
NZ_CP013673_5	5.58\|1659911\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659911-1659942	32	MH479913	Gordonia phage Fryberger, complete genome	38788-38819	8	0.75
NZ_CP013673_5	5.58\|1659911\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659911-1659942	32	MN813698	Gordonia phage Volt, complete genome	40096-40127	8	0.75
NZ_CP013673_5	5.58\|1659911\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659911-1659942	32	MH479925	Gordonia phage Ronaldo, complete genome	39932-39963	8	0.75
NZ_CP013673_5	5.58\|1659911\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659911-1659942	32	MK919478	Gordonia phage Ziko, complete genome	39918-39949	8	0.75
NZ_CP013673_5	5.75\|1661034\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661034-1661065	32	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	898572-898603	8	0.75
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	FJ937737	Burkholderia cenocepacia phage BcepIL02, complete genome	54579-54611	8	0.758
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_005262	Burkholderia cepacia phage Bcep22, complete genome	55621-55653	8	0.758
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_012743	Burkholderia phage BcepIL02, complete genome	54579-54611	8	0.758
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	NC_014811	Mycolicibacterium gilvum Spyr1 plasmid pMSPYR101, complete sequence	128311-128344	8	0.765
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	MT276994	Aeromonas phage AhyVDH1, complete genome	21065-21098	8	0.765
NZ_CP013673_5	5.107\|1663150\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1663150-1663182	33	HM486077	Tsukamurella phage TPA2, complete sequence	38623-38655	8	0.758
NZ_CP013673_5	5.107\|1663150\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1663150-1663182	33	NC_015210	Tsukamurella phage TPA2, complete genome	38623-38655	8	0.758
NZ_CP013673_5	5.21\|1657461\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657461-1657493	33	NC_015513	Haliscomenobacter hydrossis DSM 1100 plasmid pHALHY03, complete sequence	64594-64626	9	0.727
NZ_CP013673_5	5.22\|1657526\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657526-1657560	35	NC_020548	Azoarcus sp. KH32C plasmid pAZKH, complete sequence	634256-634290	9	0.743
NZ_CP013673_5	5.36\|1658456\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658456-1658489	34	MH576966	Mycobacterium phage Thyatira, complete genome	27448-27481	9	0.735
NZ_CP013673_5	5.39\|1658656\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658656-1658689	34	NZ_CP048281	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence	214850-214883	9	0.735
NZ_CP013673_5	5.40\|1658722\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658722-1658755	34	NZ_CP048281	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence	214850-214883	9	0.735
NZ_CP013673_5	5.50\|1659384\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659384-1659417	34	NZ_CP049837	Gordonia terrae strain RL-JC02 plasmid pPAE01, complete sequence	45662-45695	9	0.735
NZ_CP013673_5	5.55\|1659712\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659712-1659744	33	NC_010373	Methylobacterium sp. 4-46 plasmid pM44601, complete sequence	38916-38948	9	0.727
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013524	Rhizobium phaseoli strain R744 plasmid pRphaR744b, complete sequence	50703-50738	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013576	Rhizobium phaseoli strain N671 plasmid pRphaN671b, complete sequence	61751-61786	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013548	Rhizobium phaseoli strain R611 plasmid pRetR611a, complete sequence	61750-61785	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013528	Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence	63237-63272	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013533	Rhizobium phaseoli strain R650 plasmid pRphaR650a, complete sequence	61750-61785	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013543	Rhizobium phaseoli strain R620 plasmid pRphaR620a, complete sequence	65160-65195	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013581	Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence	63237-63272	9	0.75
NZ_CP013673_5	5.71\|1660769\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660769-1660804	36	NZ_CP013570	Rhizobium phaseoli strain N771 plasmid pRphaN771b, complete sequence	61751-61786	9	0.75
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP026091	Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence	1658854-1658886	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	482749-482781	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP026093	Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence	1658991-1659023	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	1539343-1539375	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	1658568-1658600	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP026308	Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence	1658514-1658546	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	337778-337810	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	361708-361740	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	527503-527535	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	359351-359383	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	MN369759	Mycobacterium phage Mithril, complete genome	57615-57647	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	MT818419	Mycobacterium phage Lolalove, complete genome	57461-57493	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	MK524486	Mycobacterium phage Waleliano, complete genome	57492-57524	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_008195	Mycobacterium phage Cooper, complete genome	56879-56911	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_042034	Mycobacterium phage ChrisnMich, complete sequence	56406-56438	9	0.727
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_028968	Mycobacterium phage BrownCNA, complete genome	57760-57792	9	0.727
NZ_CP013673_5	5.91\|1662089\|32\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662089-1662120	32	NZ_CP047617	Lactococcus raffinolactis strain Lr_19_5 plasmid pLraf_19_5_1, complete sequence	44114-44145	9	0.719
NZ_CP013673_5	5.95\|1662353\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662353-1662385	33	NC_013502	Rhodothermus marinus DSM 4252 plasmid pRMAR01, complete sequence	13820-13852	9	0.727
NZ_CP013673_5	5.104\|1662949\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662949-1662982	34	NC_010891	Pseudomonas sp. CT14 plasmid pCT14, complete sequence	42992-43025	9	0.735
NZ_CP013673_5	5.124\|1664275\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664275-1664308	34	NZ_CP020540	Sphingobium herbicidovorans strain MH plasmid pSHV1, complete sequence	80070-80103	9	0.735
NZ_CP013673_5	5.124\|1664275\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664275-1664308	34	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	1284380-1284413	9	0.735
NZ_CP013673_5	5.124\|1664275\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664275-1664308	34	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	1116904-1116937	9	0.735
NZ_CP013673_5	5.124\|1664275\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664275-1664308	34	NZ_CP015988	Sphingobium sp. EP60837 plasmid pEP1, complete sequence	235172-235205	9	0.735
NZ_CP013673_5	5.125\|1664341\|36\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1664341-1664376	36	NC_018023	Mycolicibacterium chubuense NBB4 plasmid pMYCCH.02, complete sequence	130408-130443	9	0.75
NZ_CP013673_5	5.154\|1666269\|37\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666269-1666305	37	MH707430	Bacillus phage BSP7, complete genome	33708-33744	9	0.757
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP041048	Citrobacter sp. CF971 plasmid pBM527-2, complete sequence	118835-118867	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	MN783744	Klebsiella oxytoca plasmid pFDL-VIM, complete sequence	16265-16297	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP037442	Klebsiella sp. PO552 plasmid p1, complete sequence	148192-148224	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP024875	Klebsiella pneumoniae strain NH25 plasmid pNH25.1, complete sequence	137980-138012	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP026154	Klebsiella pneumoniae strain F10(AN) plasmid pF10AN_1, complete sequence	175829-175861	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	MN783743	Escherichia coli plasmid pGA_VIM, complete sequence	22682-22714	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP034084	Klebsiella pneumoniae subsp. pneumoniae strain R210-2 plasmid pR210-2-VIM, complete sequence	123308-123340	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_MH220284	Aeromonas sp. pRIVM0001_VIM-1 plasmid pRIVM0001_VIM-1_171012_B12, complete sequence	128307-128339	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	HG918041	Klebsiella pneumoniae Kp15 plasmid pENVA complete sequence	14376-14408	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_MG228427	Kluyvera cryocrescens strain BO64W plasmid pKC-BO-N1-VIM, complete sequence	116343-116375	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_MH594478	Citrobacter freundii strain AA593 plasmid pIBAC_Incx3_A/C, complete sequence	1608-1640	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_MH594477	Citrobacter freundii strain AA535 plasmid pIBAC_IncA/C, complete sequence	140507-140539	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP024891	Rhodococcus ruber strain YYL plasmid pYYL1.2, complete sequence	52737-52769	9	0.727
NZ_CP013673_5	5.157\|1666469\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666469-1666501	33	NZ_CP024892	Rhodococcus ruber strain YYL plasmid pYYL1.1, complete sequence	100590-100622	9	0.727
NZ_CP013673_5	5.12\|1656864\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1656864-1656897	34	NZ_LR134447	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 5, complete sequence	218427-218460	10	0.706
NZ_CP013673_5	5.22\|1657526\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657526-1657560	35	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	1704685-1704719	10	0.714
NZ_CP013673_5	5.31\|1658124\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658124-1658157	34	NZ_LR594691	Variovorax sp. WDL1 plasmid 3	358532-358565	10	0.706
NZ_CP013673_5	5.31\|1658124\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658124-1658157	34	NZ_LR594664	Variovorax sp. RA8 plasmid 3	112826-112859	10	0.706
NZ_CP013673_5	5.39\|1658656\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658656-1658689	34	NC_015059	Granulicella tundricola MP5ACTX9 plasmid pACIX904, complete sequence	16460-16493	10	0.706
NZ_CP013673_5	5.40\|1658722\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658722-1658755	34	NC_015059	Granulicella tundricola MP5ACTX9 plasmid pACIX904, complete sequence	16460-16493	10	0.706
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	MN062185	Vibrio phage Phriendly, complete genome	15383-15416	10	0.706
NZ_CP013673_5	5.44\|1658987\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658987-1659021	35	NC_020062	Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence	766818-766852	10	0.714
NZ_CP013673_5	5.51\|1659450\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659450-1659482	33	ASHF01000034	Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence	21010-21042	10	0.697
NZ_CP013673_5	5.59\|1659975\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659975-1660007	33	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	968305-968337	10	0.697
NZ_CP013673_5	5.59\|1659975\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1659975-1660007	33	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1164069-1164101	10	0.697
NZ_CP013673_5	5.63\|1660239\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1660239-1660273	35	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	710878-710912	10	0.714
NZ_CP013673_5	5.79\|1661296\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661296-1661329	34	NZ_CP045356	Vibrio sp. THAF64 plasmid pTHAF64_a, complete sequence	1132050-1132083	10	0.706
NZ_CP013673_5	5.79\|1661296\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661296-1661329	34	NZ_CP046163	Vibrio sp. THAF191c plasmid pTHAF191c_b, complete sequence	444466-444499	10	0.706
NZ_CP013673_5	5.79\|1661296\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661296-1661329	34	NZ_CP046066	Vibrio sp. THAF191d plasmid pTHAF191d_b, complete sequence	628756-628789	10	0.706
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	481004-481036	10	0.697
NZ_CP013673_5	5.80\|1661362\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661362-1661394	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1332252-1332284	10	0.697
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	MN119376	Streptomyces phage Geostin, complete genome	8605-8638	10	0.706
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	MH155868	Streptomyces phage FlowerPower, complete genome	8605-8638	10	0.706
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	NC_016767	Erwinia phage PEp14, complete genome	3668-3701	10	0.706
NZ_CP013673_5	5.85\|1661692\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661692-1661725	34	MN284894	Streptomyces phage Fabian, complete genome	8605-8638	10	0.706
NZ_CP013673_5	5.95\|1662353\|33\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662353-1662385	33	NZ_CP037914	Sphingomonas sp. AAP5 plasmid p213, complete sequence	109263-109295	10	0.697
NZ_CP013673_5	5.102\|1662816\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662816-1662849	34	NZ_CP015237	Rhodococcus fascians D188 plasmid unnamed2, complete sequence	24838-24871	10	0.706
NZ_CP013673_5	5.118\|1663880\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1663880-1663913	34	NC_020157	Anabaena cylindrica PCC 7122 plasmid pANACY.02, complete sequence	150668-150701	10	0.706
NZ_CP013673_5	5.143\|1665542\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1665542-1665575	34	NC_006362	Nocardia farcinica IFM 10152 plasmid pNF1, complete sequence	110051-110084	10	0.706
NZ_CP013673_5	5.152\|1666137\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666137-1666170	34	NZ_CP024907	Paraburkholderia caledonica strain PHRS4 plasmid pPHRS4, complete sequence	380557-380590	10	0.706
NZ_CP013673_5	5.161\|1666733\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666733-1666766	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	334161-334194	10	0.706
NZ_CP013673_5	5.161\|1666733\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1666733-1666766	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	847504-847537	10	0.706
NZ_CP013673_5	5.19\|1657328\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1657328-1657361	34	MN693667	Marine virus AFVG_250M836, complete genome	23686-23719	11	0.676
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NC_018223	Enterococcus faecalis D32 plasmid EFD32pB, complete sequence	18537-18570	11	0.676
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_KY303941	Enterococcus faecalis strain 3 plasmid pGTC3, complete sequence	108066-108099	11	0.676
NZ_CP013673_5	5.79\|1661296\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1661296-1661329	34	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4450724-4450757	11	0.676
NZ_CP013673_5	5.97\|1662484\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1662484-1662517	34	CP000662	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence	61758-61791	11	0.676
NZ_CP013673_5	5.118\|1663880\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1663880-1663913	34	NZ_CP013925	Acinetobacter baumannii strain KBN10P02143 plasmid pKBN10P02143, complete sequence	10592-10625	11	0.676
NZ_CP013673_5	5.38\|1658589\|35\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658589-1658623	35	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	281751-281785	12	0.657
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP040614	Campylobacter sp. CFSAN093246 plasmid unnamed, complete sequence	71803-71836	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP014745	Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence	32507-32540	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP017026	Campylobacter coli plasmid pCC14983A-1, complete sequence	56454-56487	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP014743	Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence	31247-31280	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP044176	Campylobacter coli strain AR-0411 plasmid pAR-0411, complete sequence	15822-15855	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP044176	Campylobacter coli strain AR-0411 plasmid pAR-0411, complete sequence	46379-46412	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP017417	Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-2, complete sequence	62749-62782	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP018901	Campylobacter coli strain YH502 plasmid pCOS502, complete sequence	64853-64886	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP018901	Campylobacter coli strain YH502 plasmid pCOS502, complete sequence	66213-66246	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP018901	Campylobacter coli strain YH502 plasmid pCOS502, complete sequence	67588-67621	12	0.647
NZ_CP013673_5	5.41\|1658788\|34\|NZ_CP013673\|PILER-CR,CRISPRCasFinder,CRT	1658788-1658821	34	NZ_CP025282	Campylobacter coli strain YH503 plasmid pCOS503, complete sequence	49108-49141	12	0.647

1. spacer 5.15|1657064|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KM406416 (Bifidobacterium breve strain JCM 7017 plasmid megaplasmid pMP7017, complete sequence) position: , mismatch: 0, identity: 1.0

catgcccaggaggattcggccgagcgaacggaa	CRISPR spacer
catgcccaggaggattcggccgagcgaacggaa	Protospacer
*********************************

2. spacer 5.125|1664341|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_010930 (Bifidobacterium breve plasmid pB21a, complete sequence) position: , mismatch: 0, identity: 1.0

attcaaagaccttgacgccatcaacgccgccaagat	CRISPR spacer
attcaaagaccttgacgccatcaacgccgccaagat	Protospacer
************************************

3. spacer 5.160|1666667|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH444512 (Bifidobacterium phage Willi, complete genome) position: , mismatch: 0, identity: 1.0

ccgtatcggactgcaggacatcatcaccgtcacg	CRISPR spacer
ccgtatcggactgcaggacatcatcaccgtcacg	Protospacer
**********************************

4. spacer 5.160|1666667|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK932884 (Bifidobacterium phage PMBT6, complete genome) position: , mismatch: 0, identity: 1.0

ccgtatcggactgcaggacatcatcaccgtcacg	CRISPR spacer
ccgtatcggactgcaggacatcatcaccgtcacg	Protospacer
**********************************

5. spacer 5.33|1658257|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK415409 (Phage YS1-2_2434, complete genome) position: , mismatch: 1, identity: 0.971

aaacctatggtcgatcagattacagagatgtatga	CRISPR spacer
aaacctatggtcgatcagattacggagatgtatga	Protospacer
***********************.***********

6. spacer 5.58|1659911|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK415409 (Phage YS1-2_2434, complete genome) position: , mismatch: 1, identity: 0.969

acgtagggaaacacgttgtcgtaggtgtcgtg	CRISPR spacer
acgtaggggaacacgttgtcgtaggtgtcgtg	Protospacer
********.***********************

7. spacer 1.5|171771|24|NZ_CP013673|CRISPRCasFinder matches to NZ_CP047177 (Rathayibacter sp. VKM Ac-2759 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.875

atcggttccgcagccggctgccgg	CRISPR spacer
atcggttccgcagcgggcagccgt	Protospacer
************** *** ****

8. spacer 5.133|1664871|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN856058 (Myoviridae sp. isolate 283, complete genome) position: , mismatch: 3, identity: 0.914

tcgggcat-aaaaaaccacccgtgcgggtggttggg	CRISPR spacer
-cgggcataaaaaaaccacccgtgcgggtggttgaa	Protospacer
 ******* *************************..

9. spacer 5.133|1664871|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MT006237 (Bifidobacterium phage BigBern1, complete genome) position: , mismatch: 3, identity: 0.914

tcgggcat-aaaaaaccacccgtgcgggtggttggg	CRISPR spacer
-cgggcataaaaaaaccacccgtgcgggtggttgaa	Protospacer
 ******* *************************..

10. spacer 1.5|171771|24|NZ_CP013673|CRISPRCasFinder matches to NZ_CP013110 (Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence) position: , mismatch: 4, identity: 0.833

atcggttccgcagccggctgccgg	CRISPR spacer
gtcggttccgccgccggctgcctc	Protospacer
.********** **********

11. spacer 5.4|1656332|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK415409 (Phage YS1-2_2434, complete genome) position: , mismatch: 4, identity: 0.882

ctagataatcgtctaggctgatgtcttgcggctt	CRISPR spacer
ctagataatcgtcaagactgatgtcttgcggttc	Protospacer
************* **.**************.*.

12. spacer 5.8|1656598|37|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK415409 (Phage YS1-2_2434, complete genome) position: , mismatch: 4, identity: 0.892

cgttcgtcagatacaccgtatccgcgtacccgttatt	CRISPR spacer
cgttcgtcagatacaccgaatccgcgtccccgttgtc	Protospacer
****************** ******** ******.*.

13. spacer 5.42|1658854|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK415409 (Phage YS1-2_2434, complete genome) position: , mismatch: 4, identity: 0.886

cttgcctctccgaccacgcgcgggtcaaacatcga	CRISPR spacer
ttggcttctccgaccacgcgcgggtcgaacatcga	Protospacer
.* **.********************.********

14. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_010625 (Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence) position: , mismatch: 6, identity: 0.818

-gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cgtgctcca-atcgggggcggcgttgaagccgat	Protospacer
 ** * **. **.** ******************

15. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP025811 (Sulfitobacter sp. SK025 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.788

gatgccctggccgtcgatcttgccgacgacggc	CRISPR spacer
ggtctgctggccttcgatcttgcagacgacggg	Protospacer
*.* . ****** ********** ********

16. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015738 (Shinella sp. HZN7 plasmid pShin-02, complete sequence) position: , mismatch: 7, identity: 0.788

gatgccctggccgtcgatcttgccgacgacggc	CRISPR spacer
gatcggattgccgttgatcttgccgacgagggc	Protospacer
***    * *****.************** ***

17. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP035092 (Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.788

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ggcggcgcgcagccagccggcagggtcgtccat	Protospacer
*.  ****** ********** *********..

18. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_008688 (Paracoccus denitrificans PD1222 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.788

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ggcggcgcgcagccagccggcagggtcgtccat	Protospacer
*.  ****** ********** *********..

19. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.788

gaacgcgcgccgccagccggccgggtcgtccgc-	CRISPR spacer
gaacgcgcgccgccggtcggccggg-agcacgtg	Protospacer
**************.*.********  *. **.

20. spacer 5.19|1657328|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to KX683428 (Mycobacterium phage TBond007, complete genome) position: , mismatch: 8, identity: 0.765

aaacgaggcacaggagccgcaaggg-aacgagccc	CRISPR spacer
gaacgtggcacagcagccgcaagggcagcaaggt-	Protospacer
.**** ******* *********** *.*.** .

21. spacer 5.19|1657328|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_042325 (Mycobacterium virus Pixie, complete genome) position: , mismatch: 8, identity: 0.765

aaacgaggcacaggagccgcaaggg-aacgagccc	CRISPR spacer
gaacgtggcacagcagccgcaagggcagcaaggt-	Protospacer
.**** ******* *********** *.*.** .

22. spacer 5.36|1658456|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MG962374 (Mycobacterium phage Paola, complete genome) position: , mismatch: 8, identity: 0.765

-gctgattccacgtgtccggcgtgccgaaaatggc	CRISPR spacer
cgtcga-cccacgtgtccggcgtgccgacaatcag	Protospacer
 *..** .******************** *** .

23. spacer 5.36|1658456|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH051255 (Mycobacterium phage Leston, complete genome) position: , mismatch: 8, identity: 0.765

-gctgattccacgtgtccggcgtgccgaaaatggc	CRISPR spacer
cgtcga-cccacgtgtccggcgtgccgacaatcag	Protospacer
 *..** .******************** *** .

24. spacer 5.36|1658456|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MF185720 (Mycobacterium phage Guillsminger, complete genome) position: , mismatch: 8, identity: 0.765

-gctgattccacgtgtccggcgtgccgaaaatggc	CRISPR spacer
cgtcga-cccacgtgtccggcgtgccgacaatcag	Protospacer
 *..** .******************** *** .

25. spacer 5.39|1658656|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP025613 (Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.765

tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
cgtccagcttcttcttggcggcttccttgtcgat	Protospacer
..** . ****** .******************

26. spacer 5.40|1658722|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP025613 (Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.765

tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
cgtccagcttcttcttggcggcttccttgtcgat	Protospacer
..** . ****** .******************

27. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN694293 (Marine virus AFVG_250M335, complete genome) position: , mismatch: 8, identity: 0.758

gatgccctggccgtcgatcttgccgacgacggc	CRISPR spacer
atgatcctggccgtcgaacttggcgacgacgtc	Protospacer
.  ..************ **** ******** *

28. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_009427 (Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence) position: , mismatch: 8, identity: 0.758

gatgccctggccgtcgatcttgccgacgacggc	CRISPR spacer
ggcgagctgggcgtcgatcttgccgaagacctc	Protospacer
*..*  **** *************** ***  *

29. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039697 (Novosphingobium sp. ABRDHK2 plasmid pABRDHK22, complete sequence) position: , mismatch: 8, identity: 0.758

gatgccctggccgtcgatcttgccg-acgacggc	CRISPR spacer
gatgcgctggccgtcgatctcgccacgctgcag-	Protospacer
***** **************.***. .* .*.*

30. spacer 5.58|1659911|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH479913 (Gordonia phage Fryberger, complete genome) position: , mismatch: 8, identity: 0.75

acgtagggaaacacgttgtcgtaggtgtcgtg	CRISPR spacer
gcacagtcgaacacgttgtcgtagctctcgtg	Protospacer
.*..**  .*************** * *****

31. spacer 5.58|1659911|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN813698 (Gordonia phage Volt, complete genome) position: , mismatch: 8, identity: 0.75

acgtagggaaacacgttgtcgtaggtgtcgtg	CRISPR spacer
gcacagtcgaacacgttgtcgtagctctcgtg	Protospacer
.*..**  .*************** * *****

32. spacer 5.58|1659911|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH479925 (Gordonia phage Ronaldo, complete genome) position: , mismatch: 8, identity: 0.75

acgtagggaaacacgttgtcgtaggtgtcgtg	CRISPR spacer
gcacagtcgaacacgttgtcgtagctctcgtg	Protospacer
.*..**  .*************** * *****

33. spacer 5.58|1659911|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK919478 (Gordonia phage Ziko, complete genome) position: , mismatch: 8, identity: 0.75

acgtagggaaacacgttgtcgtaggtgtcgtg	CRISPR spacer
gcacagtcgaacacgttgtcgtagctctcgtg	Protospacer
.*..**  .*************** * *****

34. spacer 5.75|1661034|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

cactcgtccagcagccgagggcttcgtggcgt	CRISPR spacer
tgctcgaccagcagccgagcgcttcgtccgga	Protospacer
..**** ************ *******   *

35. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to FJ937737 (Burkholderia cenocepacia phage BcepIL02, complete genome) position: , mismatch: 8, identity: 0.758

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
catcgcgcgctgcgagccggccgggtcgatgcc	Protospacer
 * *******.** ************** .  *

36. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_005262 (Burkholderia cepacia phage Bcep22, complete genome) position: , mismatch: 8, identity: 0.758

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
catcgcgcgctgcgagccggccgggtcgatgcc	Protospacer
 * *******.** ************** .  *

37. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_012743 (Burkholderia phage BcepIL02, complete genome) position: , mismatch: 8, identity: 0.758

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
catcgcgcgctgcgagccggccgggtcgatgcc	Protospacer
 * *******.** ************** .  *

38. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_014811 (Mycolicibacterium gilvum Spyr1 plasmid pMSPYR101, complete sequence) position: , mismatch: 8, identity: 0.765

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
cggtgatggcctccacggtgctcacgccgtggcc	Protospacer
***** ****** ***********. .  ***.*

39. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MT276994 (Aeromonas phage AhyVDH1, complete genome) position: , mismatch: 8, identity: 0.765

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
cgccgatggcctgaacggcgctcatctgcttctg	Protospacer
** .* ******* ****.***********  *

40. spacer 5.107|1663150|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to HM486077 (Tsukamurella phage TPA2, complete sequence) position: , mismatch: 8, identity: 0.758

ccagcttctggttccccgtcggcttggcggacg	CRISPR spacer
cgtccttctcgttcaccgtcggcttggccgggg	Protospacer
*   ***** **** ************* *. *

41. spacer 5.107|1663150|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_015210 (Tsukamurella phage TPA2, complete genome) position: , mismatch: 8, identity: 0.758

ccagcttctggttccccgtcggcttggcggacg	CRISPR spacer
cgtccttctcgttcaccgtcggcttggccgggg	Protospacer
*   ***** **** ************* *. *

42. spacer 5.21|1657461|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_015513 (Haliscomenobacter hydrossis DSM 1100 plasmid pHALHY03, complete sequence) position: , mismatch: 9, identity: 0.727

acaagcgacacgctctatttttgttacagagat	CRISPR spacer
tccggcgaaacgctctatttttgttacacttca	Protospacer
 * .**** *******************

43. spacer 5.22|1657526|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_020548 (Azoarcus sp. KH32C plasmid pAZKH, complete sequence) position: , mismatch: 9, identity: 0.743

ggcgacaccatcatggacgccatcatcccgaccat	CRISPR spacer
gcgcaccacatcatgggggccatcatcccgaccca	Protospacer
*   **  ********. ***************

44. spacer 5.36|1658456|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH576966 (Mycobacterium phage Thyatira, complete genome) position: , mismatch: 9, identity: 0.735

-gctgattccacgtgtccggcgtgccgaaaatggc	CRISPR spacer
cgtcga-cccacatgtccggcgtgccgacaatcag	Protospacer
 *..** .****.*************** *** .

45. spacer 5.39|1658656|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP048281 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence) position: , mismatch: 9, identity: 0.735

---tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
acaacacagccttt---ctggcggcttgcttgtcgag	Protospacer
      *.*****.   ********** *********

46. spacer 5.40|1658722|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP048281 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence) position: , mismatch: 9, identity: 0.735

---tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
acaacacagccttt---ctggcggcttgcttgtcgag	Protospacer
      *.*****.   ********** *********

47. spacer 5.50|1659384|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049837 (Gordonia terrae strain RL-JC02 plasmid pPAE01, complete sequence) position: , mismatch: 9, identity: 0.735

ccgcgttgctgatgccccacaattggccgttcca	CRISPR spacer
accaggggctgatggcccaccattggccgttgcc	Protospacer
 *  *  ******* ***** ********** *

48. spacer 5.55|1659712|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_010373 (Methylobacterium sp. 4-46 plasmid pM44601, complete sequence) position: , mismatch: 9, identity: 0.727

gatgccctggccgtcgatcttgccgacgacggc	CRISPR spacer
cccgccctggccgtcgatcgtgccgtcgcccat	Protospacer
  .**************** ***** ** * ..

49. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013524 (Rhizobium phaseoli strain R744 plasmid pRphaR744b, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

50. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013576 (Rhizobium phaseoli strain N671 plasmid pRphaN671b, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

51. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013548 (Rhizobium phaseoli strain R611 plasmid pRetR611a, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

52. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013528 (Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

53. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013533 (Rhizobium phaseoli strain R650 plasmid pRphaR650a, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

54. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013543 (Rhizobium phaseoli strain R620 plasmid pRphaR620a, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

55. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013581 (Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

56. spacer 5.71|1660769|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013570 (Rhizobium phaseoli strain N771 plasmid pRphaN771b, complete sequence) position: , mismatch: 9, identity: 0.75

ttgttgtccttggcgcgtttctcccattcgcgggaa	CRISPR spacer
cccgcggccttggcgcgtctcgcccattcgcgggga	Protospacer
..  .* ***********.** ************.*

57. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026091 (Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

58. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

59. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026093 (Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

60. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

61. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

62. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026308 (Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

63. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

64. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

65. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

66. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
cgcggctcgccgccggccggccgggtcgtgatc	Protospacer
 .  ** *******.**************   *

67. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN369759 (Mycobacterium phage Mithril, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccaggcagccgggtcagcctt	Protospacer
  .************* *.********. ** .

68. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MT818419 (Mycobacterium phage Lolalove, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccaggcagccgggtcagcctt	Protospacer
  .************* *.********. ** .

69. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MK524486 (Mycobacterium phage Waleliano, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccaggcagccgggtcagcctt	Protospacer
  .************* *.********. ** .

70. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_008195 (Mycobacterium phage Cooper, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccacgcggccgggtcagcctt	Protospacer
  .************  **********. ** .

71. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_042034 (Mycobacterium phage ChrisnMich, complete sequence) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccaggctgccgggtcagcctt	Protospacer
  .************* * ********. ** .

72. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_028968 (Mycobacterium phage BrownCNA, complete genome) position: , mismatch: 9, identity: 0.727

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
ctgcgcgcgccgccaggcagccgggtcagcctt	Protospacer
  .************* *.********. ** .

73. spacer 5.91|1662089|32|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP047617 (Lactococcus raffinolactis strain Lr_19_5 plasmid pLraf_19_5_1, complete sequence) position: , mismatch: 9, identity: 0.719

ttgttggctccatcataggtattcccaattgg	CRISPR spacer
cggtccagtccatcataggtattatcaattgt	Protospacer
. **. . *************** .******

74. spacer 5.95|1662353|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_013502 (Rhodothermus marinus DSM 4252 plasmid pRMAR01, complete sequence) position: , mismatch: 9, identity: 0.727

catcacgtcggagatggtctgctggtcggcgtt	CRISPR spacer
gttgatgtcggtgatggtctgcaggtcggcaaa	Protospacer
  * *.***** ********** *******.

75. spacer 5.104|1662949|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_010891 (Pseudomonas sp. CT14 plasmid pCT14, complete sequence) position: , mismatch: 9, identity: 0.735

gacaggtcaacaacaactgcctcgtgtccggcgt	CRISPR spacer
tgcactgcggcaccaactgcctcgtgtgcggcgt	Protospacer
 .**   *..** ************** ******

76. spacer 5.124|1664275|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP020540 (Sphingobium herbicidovorans strain MH plasmid pSHV1, complete sequence) position: , mismatch: 9, identity: 0.735

ggctca---tctccgacgaggtggcgcaggccaacga	CRISPR spacer
---ccaagctctccgaagcggtggcgcaggccaagct	Protospacer
   .**   ******* * ***************

77. spacer 5.124|1664275|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 9, identity: 0.735

ggctcatctccgacgaggtggcgcaggccaacga	CRISPR spacer
tcctcatctccgacgaggtgccggaggtctattt	Protospacer
  ****************** ** ***.* *.

78. spacer 5.124|1664275|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 9, identity: 0.735

ggctcatctccgacgaggtggcgcaggccaacga	CRISPR spacer
tcctcatctccgacgaggtgccggaggtctattt	Protospacer
  ****************** ** ***.* *.

79. spacer 5.124|1664275|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015988 (Sphingobium sp. EP60837 plasmid pEP1, complete sequence) position: , mismatch: 9, identity: 0.735

ggctca---tctccgacgaggtggcgcaggccaacga	CRISPR spacer
---ccaagctctccgaagcggtggcgcaggccaagct	Protospacer
   .**   ******* * ***************

80. spacer 5.125|1664341|36|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_018023 (Mycolicibacterium chubuense NBB4 plasmid pMYCCH.02, complete sequence) position: , mismatch: 9, identity: 0.75

attcaaagaccttgacgccatcaacgccgccaagat	CRISPR spacer
ggacgaagaccttgacgccatcatcgccgccaccgg	Protospacer
.  *.****************** ********  .

81. spacer 5.154|1666269|37|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH707430 (Bacillus phage BSP7, complete genome) position: , mismatch: 9, identity: 0.757

tcgtcga-----tttaccagttcctggatcaccatagattac	CRISPR spacer
-----gataagttttaccagcacctggatcaccatagataat	Protospacer
     **     ********. ***************** *.

82. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP041048 (Citrobacter sp. CF971 plasmid pBM527-2, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

83. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN783744 (Klebsiella oxytoca plasmid pFDL-VIM, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

84. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP037442 (Klebsiella sp. PO552 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

85. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024875 (Klebsiella pneumoniae strain NH25 plasmid pNH25.1, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

86. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026154 (Klebsiella pneumoniae strain F10(AN) plasmid pF10AN_1, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

87. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN783743 (Escherichia coli plasmid pGA_VIM, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

88. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP034084 (Klebsiella pneumoniae subsp. pneumoniae strain R210-2 plasmid pR210-2-VIM, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

89. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MH220284 (Aeromonas sp. pRIVM0001_VIM-1 plasmid pRIVM0001_VIM-1_171012_B12, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

90. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to HG918041 (Klebsiella pneumoniae Kp15 plasmid pENVA complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

91. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MG228427 (Kluyvera cryocrescens strain BO64W plasmid pKC-BO-N1-VIM, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

92. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MH594478 (Citrobacter freundii strain AA593 plasmid pIBAC_Incx3_A/C, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

93. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MH594477 (Citrobacter freundii strain AA535 plasmid pIBAC_IncA/C, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
cggggccgcaatggcggcggcgctgaaggccgt	Protospacer
    ****** ***********.***** * .*

94. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024891 (Rhodococcus ruber strain YYL plasmid pYYL1.2, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
caccccggcattggcggcggggttgacgccggg	Protospacer
  .* * ************* ***** ****.

95. spacer 5.157|1666469|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024892 (Rhodococcus ruber strain YYL plasmid pYYL1.1, complete sequence) position: , mismatch: 9, identity: 0.727

gttcgccgcattggcggcggcgttgaagccgat	CRISPR spacer
caccccggcattggcggcggggttgacgccggg	Protospacer
  .* * ************* ***** ****.

96. spacer 5.12|1656864|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR134447 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 5, complete sequence) position: , mismatch: 10, identity: 0.706

cgacggcacggccacgttccggtcggacgcggtt	CRISPR spacer
gtagatctcggccacgttccggccggccgcggcc	Protospacer
  * . * **************.*** *****..

97. spacer 5.22|1657526|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 10, identity: 0.714

ggcgacaccatcatggacgccatcatcccgaccat	CRISPR spacer
ggcaacaccatcaaggacgccatcaagagcgccgg	Protospacer
***.********* ***********     .**.

98. spacer 5.31|1658124|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR594691 (Variovorax sp. WDL1 plasmid 3) position: , mismatch: 10, identity: 0.706

gcaacatcaccaccatctgggtgccggcgatcaa	CRISPR spacer
cgggcctgaccaacatctgggtgccgccgatccg	Protospacer
  ..* * **** ************* ***** .

99. spacer 5.31|1658124|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR594664 (Variovorax sp. RA8 plasmid 3) position: , mismatch: 10, identity: 0.706

gcaacatcaccaccatctgggtgccggcgatcaa	CRISPR spacer
cgggcctgaccaacatctgggtgccgccgatccg	Protospacer
  ..* * **** ************* ***** .

100. spacer 5.39|1658656|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_015059 (Granulicella tundricola MP5ACTX9 plasmid pACIX904, complete sequence) position: , mismatch: 10, identity: 0.706

tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
tctcggccttcttgctggcagctcccgcttttct	Protospacer
* *****************.***.** . *.

101. spacer 5.40|1658722|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_015059 (Granulicella tundricola MP5ACTX9 plasmid pACIX904, complete sequence) position: , mismatch: 10, identity: 0.706

tatcggccttcttgctggcggcttccttgtcgag	CRISPR spacer
tctcggccttcttgctggcagctcccgcttttct	Protospacer
* *****************.***.** . *.

102. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN062185 (Vibrio phage Phriendly, complete genome) position: , mismatch: 10, identity: 0.706

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
ctctctgcttctttctttttaagttcttcaagta	Protospacer
*.   .* ************ **** ****** .

103. spacer 5.44|1658987|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_020062 (Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence) position: , mismatch: 10, identity: 0.714

gtctacgttgtccatctgagttaccaactgagcca	CRISPR spacer
ttcgacgtcgtccatctgagttaccacgtccagaa	Protospacer
 ** ****.*****************  *  .  *

104. spacer 5.51|1659450|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to ASHF01000034 (Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence) position: , mismatch: 10, identity: 0.697

ttcacgcgccgtgttcatttgcaagacgatggt	CRISPR spacer
ggtcctcgccgagttcattcgcaagacgatccg	Protospacer
  . * ***** *******.**********

105. spacer 5.59|1659975|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 10, identity: 0.697

cacgcaagggctgttgatggcgtcgcccgcctt	CRISPR spacer
gtcctcgacgctgtcgatggcgacgcccgcctt	Protospacer
  * . .. *****.******* **********

106. spacer 5.59|1659975|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 10, identity: 0.697

cacgcaagggctgttgatggcgtcgcccgcctt	CRISPR spacer
gtcctcgacgctgtcgatggcgacgcccgcctt	Protospacer
  * . .. *****.******* **********

107. spacer 5.63|1660239|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

gatatcaccgccacgctgttcggcgtgtccggcaa	CRISPR spacer
gacaccaccgccacgctgttcggcgaccccacgct	Protospacer
**.*.********************  .**.

108. spacer 5.79|1661296|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP045356 (Vibrio sp. THAF64 plasmid pTHAF64_a, complete sequence) position: , mismatch: 10, identity: 0.706

cggtctggctgccgccctcgctg-----tgcccgtcaag	CRISPR spacer
cgggctggctgtcgccctcgctgtcggttgcttt-----	Protospacer
*** *******.***********     ***..

109. spacer 5.79|1661296|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP046163 (Vibrio sp. THAF191c plasmid pTHAF191c_b, complete sequence) position: , mismatch: 10, identity: 0.706

cggtctggctgccgccctcgctg-----tgcccgtcaag	CRISPR spacer
cgggctggctgtcgccctcgctgtcggttgcttt-----	Protospacer
*** *******.***********     ***..

110. spacer 5.79|1661296|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP046066 (Vibrio sp. THAF191d plasmid pTHAF191d_b, complete sequence) position: , mismatch: 10, identity: 0.706

cggtctggctgccgccctcgctg-----tgcccgtcaag	CRISPR spacer
cgggctggctgtcgccctcgctgtcggttgcttt-----	Protospacer
*** *******.***********     ***..

111. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 10, identity: 0.697

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
caccgcgcgcggccggccggccgggtccaggaa	Protospacer
 * ******* ***.************    .

112. spacer 5.80|1661362|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 10, identity: 0.697

gaacgcgcgccgccagccggccgggtcgtccgc	CRISPR spacer
caccgcgcgcggccggccggccgggtccaggaa	Protospacer
 * ******* ***.************    .

113. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN119376 (Streptomyces phage Geostin, complete genome) position: , mismatch: 10, identity: 0.706

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
tcaggttggcctgcatggcgctcatctggtcgag	Protospacer
. . ***********.**.********* * *

114. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MH155868 (Streptomyces phage FlowerPower, complete genome) position: , mismatch: 10, identity: 0.706

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
tcaggttggcctgcatggcgctcatctggtcgag	Protospacer
. . ***********.**.********* * *

115. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_016767 (Erwinia phage PEp14, complete genome) position: , mismatch: 10, identity: 0.706

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
cggtgttggcctgcacggtacccagaccaccgcc	Protospacer
*******************.*.**  .  . *.*

116. spacer 5.85|1661692|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN284894 (Streptomyces phage Fabian, complete genome) position: , mismatch: 10, identity: 0.706

cggtgttggcctgcacggtgctcatctgctggtc	CRISPR spacer
tcaggttggcctgcatggcgctcatctggtcgag	Protospacer
. . ***********.**.********* * *

117. spacer 5.95|1662353|33|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP037914 (Sphingomonas sp. AAP5 plasmid p213, complete sequence) position: , mismatch: 10, identity: 0.697

catcacgtcggagatggtctgctggtcggcgtt	CRISPR spacer
ggcgttgtcgggggtggtctgctggtcggcctc	Protospacer
 ..  .*****.*.**************** *.

118. spacer 5.102|1662816|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015237 (Rhodococcus fascians D188 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

tcataagccggtcttcttcgcgcagctcacgcga	CRISPR spacer
gtgagcgccggtcttcttcgcgtcgctcacgccc	Protospacer
 .. . ****************. ********

119. spacer 5.118|1663880|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_020157 (Anabaena cylindrica PCC 7122 plasmid pANACY.02, complete sequence) position: , mismatch: 10, identity: 0.706

atgaacaaacaccatttttaacaccacaacatat	CRISPR spacer
ccctatgaaaaccatttttaaaaccacaacatta	Protospacer
 .  *..** *********** **********

120. spacer 5.143|1665542|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_006362 (Nocardia farcinica IFM 10152 plasmid pNF1, complete sequence) position: , mismatch: 10, identity: 0.706

tctcgcactgcccgaggggctggacaccggtagt	CRISPR spacer
gctcgctctgcccgaagggctggacgtcgccgcc	Protospacer
 ***** ********.*********..** .. .

121. spacer 5.152|1666137|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024907 (Paraburkholderia caledonica strain PHRS4 plasmid pPHRS4, complete sequence) position: , mismatch: 10, identity: 0.706

atgcggccgcgacctacatcggcaaggtgtcgaa	CRISPR spacer
gcgcggacgcgaccgacatcggcaagacgatcca	Protospacer
..**** ******* ***********..* .  *

122. spacer 5.161|1666733|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 10, identity: 0.706

tatccgctcgcccaagaacggcggcgacgaactc	CRISPR spacer
cggccgcccgcccaagcacggcggcgagttcgtc	Protospacer
.. ****.******** **********     **

123. spacer 5.161|1666733|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 10, identity: 0.706

tatccgctcgcccaagaacggcggcgacgaactc	CRISPR spacer
cggccgcccgcccaagcacggcggcgagttcgtc	Protospacer
.. ****.******** **********     **

124. spacer 5.19|1657328|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to MN693667 (Marine virus AFVG_250M836, complete genome) position: , mismatch: 11, identity: 0.676

aaacgaggcacaggagccgcaagggaacgagccc	CRISPR spacer
gataacctcacaggagccgcaagagaaagagcta	Protospacer
.*  .   ***************.*** ****.

125. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NC_018223 (Enterococcus faecalis D32 plasmid EFD32pB, complete sequence) position: , mismatch: 11, identity: 0.676

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
tttaattattctttcttttttatatgttcaaaaa	Protospacer
.. ... ***************  *******.*.

126. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KY303941 (Enterococcus faecalis strain 3 plasmid pGTC3, complete sequence) position: , mismatch: 11, identity: 0.676

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
tttaattattctttcttttttatatgttcaaaaa	Protospacer
.. ... ***************  *******.*.

127. spacer 5.79|1661296|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 11, identity: 0.676

cggtctggctgccgccctcgctgtgcccgtcaag	CRISPR spacer
gctagtggccgccgccctcgctgtggccgccgcc	Protospacer
     ****.*************** ***.*.

128. spacer 5.97|1662484|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to CP000662 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence) position: , mismatch: 11, identity: 0.676

acaccacatgccccgacctcgcgccgaacgggct	CRISPR spacer
gtctcgagagccccgacctcgcgcggaacgagcg	Protospacer
.. .*. . *************** *****.**

129. spacer 5.118|1663880|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013925 (Acinetobacter baumannii strain KBN10P02143 plasmid pKBN10P02143, complete sequence) position: , mismatch: 11, identity: 0.676

atgaacaaacaccatttttaacaccacaacatat	CRISPR spacer
ctatgcaaacactatctttaacaccacaattagc	Protospacer
 *. .*******.**.*************.  ..

130. spacer 5.38|1658589|35|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 12, identity: 0.657

acgatcccgcgtggcgatgccgggactgctggcgt	CRISPR spacer
cgagcagggcgtggcgcagccgggactgctggcca	Protospacer
  ...   ********  ***************

131. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP040614 (Campylobacter sp. CFSAN093246 plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

132. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP014745 (Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

133. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017026 (Campylobacter coli plasmid pCC14983A-1, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atacttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

134. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP014743 (Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

135. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP044176 (Campylobacter coli strain AR-0411 plasmid pAR-0411, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

136. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP044176 (Campylobacter coli strain AR-0411 plasmid pAR-0411, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

137. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017417 (Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-2, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

138. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP018901 (Campylobacter coli strain YH502 plasmid pCOS502, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

139. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP018901 (Campylobacter coli strain YH502 plasmid pCOS502, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atatttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

140. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP018901 (Campylobacter coli strain YH502 plasmid pCOS502, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atacttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

141. spacer 5.41|1658788|34|NZ_CP013673|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP025282 (Campylobacter coli strain YH503 plasmid pCOS503, complete sequence) position: , mismatch: 12, identity: 0.647

ccgggcgattctttcttttttagttgttcaagag	CRISPR spacer
atacttatatctttcttttttagtttttaaagat	Protospacer
 ..  ..  **************** ** ****

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

53044 : 127820

uncultured_Mediterranean_phage(18.18%)

integrase,protease,tRNA

attL 124468:124527|attR 127853:127944

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_007054545.1\|53044_53890_+\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_059280526.1\|54558_55029_-	cell division protein CrgA	NA	NA	NA	NA
WP_058102064.1\|55118_55910_+	DUF881 domain-containing protein	NA	NA	NA	NA
WP_012472056.1\|55906_57145_+	class E sortase	NA	NA	NA	NA
WP_058102065.1\|57195_57840_+	anthranilate synthase	A0A0P0IKJ1	Acinetobacter_phage	1.1e-31	38.4
WP_008783610.1\|58063_60136_-	Stk1 family PASTA domain-containing Ser/Thr kinase	L7RGQ5	Acanthamoeba_polyphaga_moumouvirus	6.8e-17	33.8
WP_007055935.1\|60132_61083_-	serine/threonine protein kinase	T2AWK4	Cannes_8_virus	7.4e-19	30.7
WP_007051711.1\|61079_62546_-	penicillin-binding protein	NA	NA	NA	NA
WP_058102066.1\|62542_64204_-	cell division protein FtsW	NA	NA	NA	NA
WP_069293970.1\|64200_65895_-	phosphoprotein phosphatase	NA	NA	NA	NA
WP_007055932.1\|65899_66430_-	FHA domain-containing protein	NA	NA	NA	NA
WP_007051707.1\|66459_67161_-	DUF3662 domain-containing protein	NA	NA	NA	NA
WP_007051706.1\|67345_69790_-	prolyl oligopeptidase family serine peptidase	NA	NA	NA	NA
WP_023657990.1\|69908_71000_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_080504133.1\|71079_72231_+	VWA domain-containing protein	NA	NA	NA	NA
WP_058102068.1\|72230_72950_+	hypothetical protein	NA	NA	NA	NA
WP_007055918.1\|72946_73351_+	hypothetical protein	NA	NA	NA	NA
WP_155520183.1\|73332_73500_+	hypothetical protein	NA	NA	NA	NA
WP_012472055.1\|73462_73657_-	hypothetical protein	NA	NA	NA	NA
WP_007056809.1\|73872_74727_+	toxic anion resistance protein	A0A1S6UAV6	Serratia_phage	3.0e-19	28.1
WP_007055906.1\|75107_75611_+	Hsp20/alpha crystallin family protein	NA	NA	NA	NA
WP_058102069.1\|75937_76894_+	drug/metabolite DMT transporter permease	NA	NA	NA	NA
WP_011068559.1\|77061_77514_-	hypothetical protein	NA	NA	NA	NA
WP_077384255.1\|78364_79135_+	prolyl oligopeptidase family serine peptidase	NA	NA	NA	NA
WP_058102070.1\|79131_81705_+	DUF2156 domain-containing protein	NA	NA	NA	NA
WP_077384246.1\|81859_82108_+	hypothetical protein	NA	NA	NA	NA
WP_007051692.1\|82231_83215_+	peptide-methionine (R)-S-oxide reductase MsrB	NA	NA	NA	NA
WP_100209035.1\|83502_86697_-	DEAD/DEAH box helicase	U3PFS7	Lactobacillus_phage	2.0e-20	27.9
WP_007055916.1\|86781_87195_-	(deoxy)nucleoside triphosphate pyrophosphohydrolase	NA	NA	NA	NA
WP_007051681.1\|88257_88590_+	putative heavy metal-binding protein	NA	NA	NA	NA
WP_058102071.1\|88677_89142_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_012472051.1\|89222_90080_-	hemolysin III family protein	NA	NA	NA	NA
WP_007054515.1\|90183_90420_-	hypothetical protein	NA	NA	NA	NA
WP_007051677.1\|90479_90845_+	hypothetical protein	NA	NA	NA	NA
WP_058102072.1\|91325_92639_-\|tRNA	tRNA guanosine(34) transglycosylase Tgt	A0A1B1IVQ4	uncultured_Mediterranean_phage	6.3e-53	32.7
WP_058102073.1\|93055_95068_+\|protease	trypsin-like serine protease	A0A1B1IT49	uncultured_Mediterranean_phage	1.2e-18	28.0
WP_032741283.1\|95479_97639_+	heavy metal translocating P-type ATPase	E4ZFI9	Streptococcus_phage	2.7e-45	25.8
WP_050491744.1\|97815_98865_+	LacI family transcriptional regulator	NA	NA	NA	NA
WP_013410463.1\|98870_99131_-	hypothetical protein	NA	NA	NA	NA
WP_015512529.1\|99132_100164_-	twin-arginine translocase subunit TatC	NA	NA	NA	NA
WP_013410461.1\|100211_100502_-	twin-arginine translocase TatA/TatE family subunit	NA	NA	NA	NA
WP_013410459.1\|101181_103584_+	glycosyhydrolase	NA	NA	NA	NA
WP_015512528.1\|103673_106154_+	hypothetical protein	NA	NA	NA	NA
WP_100967826.1\|106543_107707_-	ATP-binding protein	NA	NA	NA	NA
WP_007057726.1\|107910_109362_+	glutamate synthase	NA	NA	NA	NA
WP_007055925.1\|109514_110453_+\|protease	zinc metalloprotease HtpX	NA	NA	NA	NA
WP_058102074.1\|110663_111731_-	class II fructose-bisphosphate aldolase	NA	NA	NA	NA
WP_007051668.1\|111946_113233_+	adenylosuccinate synthase	A0A285PX35	Cedratvirus	5.8e-67	35.0
WP_007054506.1\|113256_114840_+	ClC family H(+)/Cl(-) exchange transporter	NA	NA	NA	NA
WP_015713216.1\|114867_116097_+	CrcB family protein	NA	NA	NA	NA
WP_080669909.1\|115397_116492_+	CrcB family protein	NA	NA	NA	NA
WP_010081389.1\|116766_117852_+	LacI family transcriptional regulator	NA	NA	NA	NA
WP_081040142.1\|118051_119845_+	potassium transporter Kup	A7J6G4	Paramecium_bursaria_Chlorella_virus	3.6e-43	33.4
WP_007051661.1\|120261_121809_+	alpha-L-arabinofuranosidase	NA	NA	NA	NA
WP_058062454.1\|121980_123015_+	LacI family transcriptional regulator	NA	NA	NA	NA
WP_010081385.1\|123100_124108_-	hypothetical protein	NA	NA	NA	NA
124468:124527	attL	NA	NA	NA	NA
WP_007053137.1\|124603_125806_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_069293971.1\|125802_126768_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_007054866.1\|126764_127820_+\|integrase	tyrosine-type recombinase/integrase	A0A0U4IH55	Gordonia_phage	1.0e-05	26.7
127853:127944	attR	NA	NA	NA	NA

DBSCAN-SWA_2

734032 : 800477

Mycobacterium_phage(15.38%)

transposase,integrase,tRNA

attL 794842:794901|attR 798227:798322

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_058101910.1\|734032_734632_+\|tRNA	aminoacyl-tRNA hydrolase	NA	NA	NA	NA
WP_058101909.1\|734621_738206_+	transcription-repair coupling factor	NA	NA	NA	NA
WP_081040168.1\|738345_739293_+	aldo/keto reductase	NA	NA	NA	NA
WP_007051126.1\|739443_740742_+	phosphopyruvate hydratase	W6LP63	Streptococcus_phage	1.4e-132	56.2
WP_075662294.1\|740808_741426_+	septum formation initiator family protein	NA	NA	NA	NA
WP_058101906.1\|741422_741989_+	DUF501 domain-containing protein	NA	NA	NA	NA
WP_007051123.1\|742051_743053_+	Ppx/GppA family phosphatase	NA	NA	NA	NA
WP_008783747.1\|743442_744714_+\|transposase	IS30-like element ISBlo4 family transposase	W5R8L2	Staphylococcus_phage	3.5e-40	35.9
WP_011068251.1\|744845_747065_+	L-serine ammonia-lyase	NA	NA	NA	NA
WP_007051894.1\|747206_747614_+	peptidylprolyl isomerase	NA	NA	NA	NA
WP_007055115.1\|747712_748192_+	transcription elongation factor GreA	NA	NA	NA	NA
WP_007051896.1\|748246_749158_-	hemolysin III	NA	NA	NA	NA
WP_081040154.1\|749360_750089_+	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_011068248.1\|750206_751739_+	PAS domain-containing sensor histidine kinase	NA	NA	NA	NA
WP_003835265.1\|751811_752090_-	WhiB family transcriptional regulator	A0A2P1N2X5	Mycobacterium_phage	1.3e-11	45.1
WP_081040153.1\|752203_753955_-	cell division protein FtsK	A0A142F150	Bacillus_phage	2.0e-14	31.8
WP_021975633.1\|754199_755633_-	LCP family protein	NA	NA	NA	NA
WP_007051901.1\|755883_756183_+	WhiB family transcriptional regulator	A0A2P1CGA4	Mycobacterium_phage	4.1e-24	68.1
WP_058101824.1\|756226_759322_+	hypothetical protein	NA	NA	NA	NA
WP_007053571.1\|759318_760860_+	hypothetical protein	NA	NA	NA	NA
WP_007051904.1\|760962_761424_-	metallopeptidase family protein	NA	NA	NA	NA
WP_058101823.1\|761479_762286_+	HAD-IIB family hydrolase	NA	NA	NA	NA
WP_080746348.1\|762400_763018_+	ComF family protein	NA	NA	NA	NA
WP_007051907.1\|762933_763320_-	S24 family peptidase	F1C5A6	Cronobacter_phage	2.1e-09	40.8
WP_007051908.1\|763387_764464_-	HAMP domain-containing histidine kinase	A0A1V0SGX0	Hokovirus	7.6e-12	27.5
WP_007051909.1\|764460_765183_-	response regulator transcription factor	W8CYM9	Bacillus_phage	1.7e-28	33.2
WP_008782797.1\|765218_767471_-	1,4-alpha-glucan branching protein GlgB	NA	NA	NA	NA
WP_007053566.1\|767648_768242_+	CarD family transcriptional regulator	NA	NA	NA	NA
WP_007053565.1\|768350_768875_+	2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase	NA	NA	NA	NA
WP_007051913.1\|768926_769760_-	metal ABC transporter permease	NA	NA	NA	NA
WP_074709717.1\|769826_770813_-	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	1.1e-17	34.7
WP_023658186.1\|770889_772086_-	Solute-binding protein of ABC transporter system for metals	NA	NA	NA	NA
WP_007053562.1\|772189_773065_+	bifunctional methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase	NA	NA	NA	NA
WP_007051917.1\|773184_774660_+	30S ribosomal protein S1	NA	NA	NA	NA
WP_007055464.1\|774833_775451_+	dephospho-CoA kinase	NA	NA	NA	NA
WP_007051919.1\|775462_777574_+	excinuclease ABC subunit UvrB	NA	NA	NA	NA
WP_007051920.1\|777742_778729_+	TerC family protein	A0A291LBC5	Escherichia_phage	1.6e-37	34.4
WP_007055467.1\|778896_780339_+	pyruvate kinase	NA	NA	NA	NA
WP_011068238.1\|780486_781248_-	NUDIX hydrolase	NA	NA	NA	NA
WP_007052013.1\|781431_782217_+	response regulator	NA	NA	NA	NA
WP_058101822.1\|782262_785130_+	DNA polymerase I	A0A0C5K9B9	Enterococcus_phage	3.3e-38	28.9
WP_074709723.1\|785290_786220_+	Nif3-like dinuclear metal center hexameric protein	NA	NA	NA	NA
WP_012578040.1\|786265_786940_+	NUDIX hydrolase	NA	NA	NA	NA
WP_011068234.1\|786993_789135_+	glycogen debranching protein GlgX	NA	NA	NA	NA
WP_058101821.1\|789185_789416_+	hypothetical protein	NA	NA	NA	NA
WP_058101820.1\|789419_790070_+	transcriptional regulator	NA	NA	NA	NA
WP_058101819.1\|790239_790794_-	DNA-3-methyladenine glycosylase I	NA	NA	NA	NA
WP_155759152.1\|791411_791648_+	hypothetical protein	NA	NA	NA	NA
WP_058062546.1\|791880_792942_-	hypothetical protein	NA	NA	NA	NA
WP_058101817.1\|793225_793783_+	hypothetical protein	NA	NA	NA	NA
794842:794901	attL	NA	NA	NA	NA
WP_007054866.1\|794933_795989_-\|integrase	tyrosine-type recombinase/integrase	A0A0U4IH55	Gordonia_phage	1.0e-05	26.7
WP_007053138.1\|795985_796951_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_058102001.1\|796947_798150_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_116868981.1\|798280_799297_-\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	2.3e-10	30.8
798227:798322	attR	NA	NA	NA	NA
WP_014485511.1\|799631_800477_-\|transposase	IS21 family transposase	NA	NA	NA	NA

DBSCAN-SWA_3

2227736 : 2237595

Mycobacterium_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_007051809.1\|2227736_2228864_-	sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC	G9BWD6	Planktothrix_phage	2.9e-22	33.8
WP_080670006.1\|2229222_2230404_-	glycosyltransferase family 2 protein	NA	NA	NA	NA
WP_007054635.1\|2230482_2231475_-	class 1b ribonucleoside-diphosphate reductase subunit beta	R4TBI6	Mycobacterium_phage	4.7e-141	77.6
WP_058102048.1\|2231700_2233896_-	class 1b ribonucleoside-diphosphate reductase subunit alpha	V9VI16	Lactococcus_phage	1.6e-186	47.4
WP_007051804.1\|2234011_2234419_-	class Ib ribonucleoside-diphosphate reductase assembly flavoprotein NrdI	R4JF54	Bacillus_phage	1.0e-09	30.8
WP_007054638.1\|2234466_2234781_-	glutaredoxin family protein	V5R9U9	Mycobacterium_phage	6.0e-10	41.8
WP_011068608.1\|2234881_2235124_+	hypothetical protein	NA	NA	NA	NA
WP_007056537.1\|2235320_2235944_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_015713953.1\|2235954_2236635_-	DUF3990 domain-containing protein	NA	NA	NA	NA
WP_058102049.1\|2236827_2237595_+	voltage-gated potassium channel	A0A2I7SA68	Vibrio_phage	4.9e-05	27.2

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_CP013673

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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