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_CP047050	Myroides phaeus strain 18QD1AZ29W chromosome, complete genome	4 crisprs	DEDDh,csa3,WYL,cas3,cas6,cas8b1,cas7b,cas5,cas4,cas1,cas2	1	9	2	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP047050_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP047050_1

952976-953115

Orphan

Consensus_repeat	Method
TTTCATATCTGACCAGATCTATTAAACAAACTTAAATATCGAAAATAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP047050_1

>merge|NZ_CP047050|1|952976-953115|CRISPRCasFinder
TTTCATATCTGACCAGATCTATTAAACAAACTTAAATATCGAAAATATAGAGAGTCCTAAAAAAGTACTACGAAAAAATAGCTCCATATAAATTTCATATCTGACCAGATCTATTAAACAAACTTAAATATCGAAAATAT

>NZ_CP047050|1|1|952976-953115|CRISPRCasFinder
TTTCATATCTGACCAGATCTATTAAACAAACTTAAATATCGAAAATAT	AGAGAGTCCTAAAAAAGTACTACGAAAAAATAGCTCCATATAAA
TTTCATATCTGACCAGATCTATTAAACAAACTTAAATATCGAAAATAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047050.1\|WP_158209764.1\|942116_943307_-\|phosphoglycerate-kinase	unknown	unknown	gnl\|CDD\|234613
NZ_CP047050.1\|WP_158211324.1\|939544_940453_-\|DUF4837-family-protein	unknown	unknown	gnl\|CDD\|379774
NZ_CP047050.1\|WP_158209774.1\|958221_958563_-\|YtxH-domain-containing-protein	unknown	unknown	gnl\|CDD\|378938
NZ_CP047050.1\|WP_158209770.1\|954321_955836_+\|glutamate--tRNA-ligase	unknown	unknown	gnl\|CDD\|234953
NZ_CP047050.1\|WP_158209762.1\|938363_939347_+\|protein-tyrosine-phosphatase	unknown	unknown	gnl\|CDD\|379135
NZ_CP047050.1\|WP_158209771.1\|955969_956485_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158209768.1\|948103_948955_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|372616
NZ_CP047050.1\|WP_158209773.1\|957598_957844_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_090404638.1\|960482_960839_+\|dihydroneopterin-aldolase	unknown	unknown	gnl\|CDD\|376737
NZ_CP047050.1\|WP_158209763.1\|940563_942066_-\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|381615
NZ_CP047050.1\|WP_158209765.1\|943647_944796_+\|DNA-polymerase-III-subunit-delta'	unknown	unknown	gnl\|CDD\|273213
NZ_CP047050.1\|WP_158209766.1\|944869_947161_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|350795
NZ_CP047050.1\|WP_158209767.1\|947255_947852_-\|OmpH-family-outer-membrane-protein	unknown	unknown	gnl\|CDD\|214922
NZ_CP047050.1\|WP_158209777.1\|961870_962545_-\|DUF2807-domain-containing-protein	unknown	unknown	gnl\|CDD\|371327
NZ_CP047050.1\|WP_158211325.1\|949399_951271_-\|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	unknown	unknown	gnl\|CDD\|235362
NZ_CP047050.1\|WP_090404629.1\|957855_958206_-\|phage-holin-family-protein	unknown	unknown	gnl\|CDD\|377816
NZ_CP047050.1\|WP_158209772.1\|956559_957540_+\|SPFH-domain-containing-protein	unknown	unknown	gnl\|CDD\|259805
NZ_CP047050.1\|WP_158209769.1\|951314_951734_-\|rRNA-maturation-RNase-YbeY	unknown	unknown	gnl\|CDD\|272871
NZ_CP047050.1\|WP_158209776.1\|961101_961785_-\|LysE-family-transporter	unknown	unknown	gnl\|CDD\|280058
NZ_CP047050.1\|WP_158209775.1\|958671_960354_-\|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	unknown	unknown	gnl\|CDD\|235424

Protein	Function_ID	Function_description	E-value
NZ_CP047050.1\|WP_158209764.1\|942116_943307_-\|phosphoglycerate-kinase	gnl\|CDD\|234613	PRK00073, pgk, phosphoglycerate kinase; Provisional.	0
NZ_CP047050.1\|WP_158211324.1\|939544_940453_-\|DUF4837-family-protein	gnl\|CDD\|379774	pfam16125, DUF4837, Domain of unknown function (DUF4837). This family consists of uncharacterized proteins around 350 residues in length and is mainly found in various Bacteroides species. The function of this family is unknown.	4.31327e-85
NZ_CP047050.1\|WP_158209774.1\|958221_958563_-\|YtxH-domain-containing-protein	gnl\|CDD\|378938	pfam12732, YtxH, YtxH-like protein. This family of proteins is found in bacteria. Proteins in this family are typically between 100 and 143 amino acids in length. The N-terminal region is the most conserved. Proteins is this family are functionally uncharacterized.	7.4511e-12
NZ_CP047050.1\|WP_158209770.1\|954321_955836_+\|glutamate--tRNA-ligase	gnl\|CDD\|234953	PRK01406, gltX, glutamyl-tRNA synthetase; Reviewed.	0
NZ_CP047050.1\|WP_158209762.1\|938363_939347_+\|protein-tyrosine-phosphatase	gnl\|CDD\|379135	pfam13350, Y_phosphatase3, Tyrosine phosphatase family. This family is closely related to the pfam00102 and pfam00782 families.	2.15842e-81
NZ_CP047050.1\|WP_158209768.1\|948103_948955_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|372616	pfam13489, Methyltransf_23, Methyltransferase domain. This family appears to be a methyltransferase domain.	6.05294e-27
NZ_CP047050.1\|WP_090404638.1\|960482_960839_+\|dihydroneopterin-aldolase	gnl\|CDD\|376737	pfam02152, FolB, Dihydroneopterin aldolase. This enzyme EC:4.1.2.25 catalyzes the conversion of 7,8-dihydroneopterin to 6-hydroxymethyl-7,8-dihydropterin in the biosynthetic pathway of tetrahydrofolate.	5.27601e-34
NZ_CP047050.1\|WP_158209763.1\|940563_942066_-\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|381615	cd16894, MltD-like, Membrane-bound lytic murein transglycosylase D and similar proteins. Lytic transglycosylases (LT) catalyze the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc). Membrane-bound lytic murein transglycosylase D protein (MltD) family members may have one or more small LysM domains, which may contribute to peptidoglycan binding. Unlike the similar "goose-type" lysozymes, LTs also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. Proteins similar to this family include the soluble and insoluble membrane-bound LTs in bacteria, the LTs in bacteriophage lambda, as well as the eukaryotic "goose-type" lysozymes (goose egg-white lysozyme; GEWL).	6.51554e-66
NZ_CP047050.1\|WP_158209765.1\|943647_944796_+\|DNA-polymerase-III-subunit-delta'	gnl\|CDD\|273213	TIGR00678, DNA_polymerase_III_subunit_delta', DNA polymerase III, delta' subunit. This model describes the N-terminal half of the delta' subunit of DNA polymerase III. Delta' is homologous to the gamma and tau subunits, which form an outgroup for phylogenetic comparison. The gamma/tau branch of the tree is much more tighly conserved than the delta' branch, and some members of that branch score more highly against this model than some proteins classisified as delta'. The noise cutoff is set to detect weakly scoring delta' subunits rather than to exclude gamma/tau subunits. At position 126-127 of the seed alignment, this family lacks the HM motif of gamma/tau; at 132 it has a near-invariant A vs. an invariant F in gamma/tau. [DNA metabolism, DNA replication, recombination, and repair].	2.37691e-52
NZ_CP047050.1\|WP_158209766.1\|944869_947161_-\|AAA-family-ATPase	gnl\|CDD\|350795	cd18037, DEXSc_Pif1_like, DEAD-box helicase domain of Pif1. Pif1 and other members of this family are RecD-like helicases involved in maintaining genome stability through unwinding double-stranded DNAs (dsDNAs), DNA/RNA hybrids, and G quadruplex (G4) structures. The members of Pif1 helicase subfamily studied so far all appear to contribute to telomere maintenance. Pif1 is a member of the DEAD-like helicases superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	2.78038e-50
NZ_CP047050.1\|WP_158209767.1\|947255_947852_-\|OmpH-family-outer-membrane-protein	gnl\|CDD\|214922	smart00935, OmpH, Outer membrane protein (OmpH-like). This family includes outer membrane proteins such as OmpH among others. Skp (OmpH) has been characterized as a molecular chaperone that interacts with unfolded proteins as they emerge in the periplasm from the Sec translocation machinery.	2.30831e-19
NZ_CP047050.1\|WP_158209777.1\|961870_962545_-\|DUF2807-domain-containing-protein	gnl\|CDD\|371327	pfam10988, DUF2807, Putative auto-transporter adhesin, head GIN domain. This bacterial family of proteins shows structural similarity to other pectin lyase families. Although structures from this family align with acetyl-transferases, there is no conservation of catalytic residues found. It is likely that the function is one of cell-adhesion. In Structure 3jx8, it is interesting to note that the sequence of contains several well defined sequence repeats, centred around GSG motifs defining the tight beta turn between the two sheets of the super-helix; there are 8 such repeats in the C-terminal half of the protein, which could be grouped into 4 repeats of two. It seems likely that this family belongs to the superfamily of trimeric auto-transporter adhesins (TAAs), which are important virulence factors in Gram-negative pathogens. In the case of Parabacteroides distasonis, which is a component of the normal distal human gut microbiota, TAA-like complexes probably modulate adherence to the host (information derived from TOPSAN).	6.9299e-36
NZ_CP047050.1\|WP_158211325.1\|949399_951271_-\|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	gnl\|CDD\|235362	PRK05192, PRK05192, tRNA uridine-5-carboxymethylaminomethyl(34) synthesis enzyme MnmG.	0
NZ_CP047050.1\|WP_090404629.1\|957855_958206_-\|phage-holin-family-protein	gnl\|CDD\|377816	pfam07332, Phage_holin_3_6, Putative Actinobacterial Holin-X, holin superfamily III. Phage_holin_3_6 is a family of small hydrophobic proteins with two or three transmembrane domains of the Hol-X family. Holin proteins are produced by double-stranded DNA bacteriophages that use an endolysin-holin strategy to achieve lysis of their hosts. The endolysins are peptidoglycan-degrading enzymes that are usually accumulated in the cytosol until access to the cell wall substrate is provided by the holin membrane lesion.	0.000980632
NZ_CP047050.1\|WP_158209772.1\|956559_957540_+\|SPFH-domain-containing-protein	gnl\|CDD\|259805	cd03407, SPFH_like_u4, Uncharacterized family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model summarizes an uncharacterized family of proteins similar to stomatin, prohibitin, flotillin, HflK/C (SPFH) and podocin. The conserved domain common to the SPFH superfamily has also been referred to as the Band 7 domain. Many superfamily members are associated with lipid rafts. Individual proteins of the SPFH superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. Microdomains formed from flotillin proteins may in addition be dynamic units with their own regulatory functions. Flotillins have been implicated in signal transduction, vesicle trafficking, cytoskeleton rearrangement and are known to interact with a variety of proteins. Stomatin interacts with and regulates members of the degenerin/epithelia Na+ channel family in mechanosensory cells of Caenorhabditis elegans and vertebrate neurons and participates in trafficking of Glut1 glucose transporters. Prohibitin may act as a chaperone for the stabilization of mitochondrial proteins. Prokaryotic HflK/C plays a role in the decision between lysogenic and lytic cycle growth during lambda phage infection. Flotillins have been implicated in the progression of prion disease, in the pathogenesis of neurodegenerative diseases such as Parkinson's and Alzheimer's disease and, in cancer invasion and metastasis. Mutations in the podocin gene give rise to autosomal recessive steroid resistant nephritic syndrome.	3.16863e-134
NZ_CP047050.1\|WP_158209769.1\|951314_951734_-\|rRNA-maturation-RNase-YbeY	gnl\|CDD\|272871	TIGR00043, Endoribonuclease_YbeY, rRNA maturation RNase YbeY. This metalloprotein family is represented by a single member sequence only in nearly every bacterium. Crystallography demonstrated metal-binding activity, possibly to nickel. It is a predicted to be a metallohydrolase, and more recently it was shown that mutants have a ribosomal RNA processing defect. [Protein synthesis, Other].	1.06222e-29
NZ_CP047050.1\|WP_158209776.1\|961101_961785_-\|LysE-family-transporter	gnl\|CDD\|280058	pfam01810, LysE, LysE type translocator. This family consists of various hypothetical proteins and an l-lysine exporter LysE from Corynebacterium glutamicum which is proposed to be the first of a novel family of translocators. LysE exports l-lysine from the cell into the surrounding medium and is predicted to span the membrane six times. The physiological function of the exporter is to excrete excess l-Lysine as a result of natural flux imbalances or peptide hydrolysis; and also after artificial deregulation of l-Lysine biosynthesis as used by the biotechnology. industry for the production of l-lysine.	5.23459e-11
NZ_CP047050.1\|WP_158209775.1\|958671_960354_-\|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	gnl\|CDD\|235424	PRK05347, PRK05347, glutaminyl-tRNA synthetase; Provisional.	0

>NZ_CP047050.1|WP_158209769.1|951314_951734_-|rRNA-maturation-RNase-YbeY
MISFNYESDFQLDNENLYEEWIESIIASEGFYLGEISYIFCDDEYLHNINVEYLDHDTLTDIISFDYTEGKIISGDIFLSVERVRDNAKDFNVEFSTELLRVMCHGILHYCGYKDKTDEDSKLMRSKEEEKMAMFHVEQ
>NZ_CP047050.1|WP_158211325.1|949399_951271_-|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG
MFQDTYDVIVVGGGHAGSEAAAAAANMGSKTLLITMSLQNIAQMSCNPAMGGIAKGQIVREIDALGGYSGIVSDKTAIQFKMLNKSKGPAMWSPRVQSDRMRFAELWRLMLEGTPNLDFYQDMVRSLIIKNERIEGVVTNLGIEIKAKTVILTNGTFLNGLIHIGEKQFGGGRAGESAAYGITEDLVKAGFVSGRMKTGTPPRVDGRSLDYTKMEAQPGDENPAKFSYLDVTKPLVEQRDCHMTYTSPLVHELLREGFDRSPMFTGRIKSIGPRYCPSIEDKINRFADKDRHQIFVEPEGWNTCEIYVNGFSTSLPEEVQIKALRSVAGFENAKIFRPGYAIEYDYFPPTQLKHTLETKLVDGLFFAGQINGTTGYEEAAAQGLMAGMNAHLKVNGKEPFILRRDEAYIGVLIDDLITKGTEEPYRMFTSRAEYRTLLRQDNADFRLTPKSFELGLASEQRLRRMEFKREESESFVQFFKETSVKTEEANPILEEKGSSLMSQPDKMFKVFSRPQIELGDILKFKKVKEYIEEHDLDQEILEQAEIQVKYSGYIEKEKSNADKLTRLEDVKIPSNFDYDKIVSLSFESREKLKKIKPITISQASRISGVTPTDVSILLIHMGR
>NZ_CP047050.1|WP_158209768.1|948103_948955_-|methyltransferase-domain-containing-protein
MQIESNIKFLEVEDYSVSNEKFELYLDPSYHLLKTIPQPKSEELGKYYESENYISHTDKKTTFFEKVYQTIKRKAIQNKLNLLESIKESKGNLLDIGCGTGDFLAAAKNRNWNVVGYEPNLGARKLAEEKGVSIVEDTKSIEEGTLDVITLWHVLEHVPDLENQIKELYRLLKPNGILIIAVPNYKSYDAQYYGKHWAAYDVPRHLWHFSQQSIPLLFNPFGFILQDTYPMLFDSFYVSLLSEEIKHGKKNWLKAFSVGLKSNIEARRNLEYSSLIYSLKKTI
>NZ_CP047050.1|WP_158209767.1|947255_947852_-|OmpH-family-outer-membrane-protein
MKKTILMLGFAGLLFSCNNNSNAAVEFKTAYVDSSKLMKEYEEVKDVESKYKIQSEEKGKSLEADIAKFQQEVQSFQANARQKGQAWAEQKAAELQKKEQQLQYQQQAMVQSLQMESGQEIDSVVKKVKEYISEYAKKNNLDYVFNTEEASTVIYGKEQYDITESILKELNAKYKGTSAATKIDEPAVPAAEKKEETK
>NZ_CP047050.1|WP_158209766.1|944869_947161_-|AAA-family-ATPase
MNNFSEEAKFVLQFINETNRSIFLTGKAGTGKTTLLKEIIQTTHKNAVIVAPTGIAALNAGGVTIHSFFHLPFAAFVPDTKNPPIFTDNIKFENKLSLKRHMRMSRVRKALFLNMDLLVIDEVSMLRADVLDAMNFMLQSIRKNPQPFGGVQVLFIGDLLQLPPVVKQAEWDVLQRYYGGVFFFHSEVVRQFPPLYIELDKVFRQSDQEFIQILNNLRNNQVTSQDVQLLNKFIKTDFDIKNNPGYITLTTHNTKADKINKDALDGIDKKEFVFKPDVVGDFPEKLFPLEANMSLKVGAQVIFIKNDISPEKRFYNGKMGIVKSLSNNEIFVHFPEENETIEVEKYEWENIKYTVDPNTKEIVEEVLGTFTHYPLKLAWAITVHKSQGLTFDKAVLDVSSVFLPGQAYVALSRLRSLEGLVLLSPIQMNGLVNDEEVMSYANNKATVDRLTQELQLATKDFLRNFLIDTYSWFNLGTLWHAHIHTYDAETDRSKKNSFKPWAIKTTKSLNDMLIHSEKFVHQLRCLFNEENFRFAHVKERVNKAYQYFFPMMDHLVFELLFNIAQVKGKRQLKGFYEELVVLEDALLKQVIQMKKAEKMLQLLEEGKKISKENLRSLEISEYKINHLVNIANLLRDTQLDLDEDDDVSKYSSTKKGEKKEKKKSTTSITLEYWKQKKSIEEIAEIRKLVPTTIYSHLGKLVGDGLIQLDEILPKDKIDELEELFITFKDKPLSEIKATVEDLYSWEELKLFQRAKDALKESEE
>NZ_CP047050.1|WP_158209765.1|943647_944796_+|DNA-polymerase-III-subunit-delta'
MQFSDIIGQAYLKNHLIQTASTGRIPHAQLFIGPEGSGTLPMAIAYAQYLLCQNVGNENTGGNDSCNIKFNNLSHPDLHFVYPVATTDAVKRNATSDLFASQWRSFIKDNVYGNLFDWYSHIEIQNKQGQIGVDEASEVLKKLALKSFEGGYKIMIIWMADKMNTEASNKLLKLLEEPPAKTLFLLIAENVKNIIQTILSRCQVLNFPPINNREIEEALIVKQQCDRQEAALIAGQAQGSYNKALKLLLNKNSTQPYEKWFVQWVRAAFRAKGNAAVIQELIEWSEELAALGREQQKQFIEFCIELFRQALLINYQTPNLVYYKTTVDNFKLEKFAPFVNGANINDIYKELSDAIYHIERNGNAKMIFTDLSIKLTRLIHRK
>NZ_CP047050.1|WP_158209764.1|942116_943307_-|phosphoglycerate-kinase
MSSIGNLNFKDKKVLIRVDFNVPLDENFNVTDTNRIEAAKATIDKVVNDGGVAILMSHLGRPKGEVNEKYSLKHIVAKTAEVLGREVTFVNDCIGDNVKAVIDNSKSGDVILLENLRFYAQEEKGEEEFSKALASLADFYINDAFGTAHRAHASTTIVAKYFGENKCFGYLLAKEIESLDKVLNSTDKPVTAVLGGSKVSSKITIIENILDKIDHMIIGGGMTFTFIKALGGKIGNSICEDDKIELALEILEKAKEKNVQIHLPIDIVAADAFAADANVKIVAANEIPDGWQGLDVGPKTLESLKPVVAESKIILWNGPLGVFEMEKFANGTIELGNFIAEATKKGTFSLVGGGDSVAAVKQFGLAPKMSYVSTGGGAMLEMLEGKALPGIKAIQE
>NZ_CP047050.1|WP_158209763.1|940563_942066_-|LysM-peptidoglycan-binding-domain-containing-protein
MNYKALTFVVCSLFSYSVWGQSEPINTSIEIKKEIDPVVYLDSIKNTFVNHATGASIEKRWLNELLNQDLFNEIENELADANFDEGTIVLDELPTKLLKERLQRLNEKTPFKVEYNETLERVIKSFLKNRKRSFERLLGLSEYYFPMFEEQLAKHDVPLEVKYLAIVESALNPVARSRVGATGLWQFMYPTGKQYNLEVNSYVDDRIDPIKSSEAAAKFLSDLYGMFGDWDLVLASYNAGPGNVTKAIRRSNGYTNYWNIRPNLPRETQNYLPAFYATMYIFEYAKEHGITSNSSPFKLVETDTIAVKKTISFDQVAKLLDVSKAEIEFLNPTYKLQVVPYVSGKQSFLRLPVSKIGLMASNEDKIYDYIAFEEERREKPLPSLLEVSVAETKSVKSRYHTIKKGESIGVIANKYGISVAQLKKLNNMKSNIIYPGKKLVVGKATVAQSSAKNSFYTVKKGDSLYSISQKLPGVSLAQLKNMNNMKDNDAIQPGMKLRIN
>NZ_CP047050.1|WP_158211324.1|939544_940453_-|DUF4837-family-protein
MGEYNSVLVVVNDRLWYGNVGDSIREYLAASVDGISPSEPLFTIEQISPNLFSSKTKDRRNIIVFSDNHNDEFFSLEKNKFASPQNYFVVNGGSKLAVVKAFKKNIDSIIKTMHQLEVSTITETLNASKLIDREKFEDRFKITINVPSDYKEISSNEHFVWYKKDVASGNSNILIYDVPLKRILNDKDTELHNILAVKDSVNGRYIHSIEDNSFMKLNEGFIPFNKEISFDNRKAIELKGTWDMQNSFMSGPYLSYVFRDSTEKRYLFIEGLVYNPSMGKRNVLLELEAIIQTMRFKIKKSE
>NZ_CP047050.1|WP_158209762.1|938363_939347_+|protein-tyrosine-phosphatase
MGTKGSNQTIDLKTDKKNNKTIAIIKANQPWKLYKANSSFVINAAQEIASGDSNDSISLGQIASFQLFAFENNRNYDITGLRCLPLEGQNNFRDLGGYKTTEGKTVKWGLLFRSGQLSSLSERDLRYLSSIPLCTIVDFRTNEERDSQVTKLPSSTINDISLPISPGNLSREIVENMIYEGEVEQTVQFLTDINEQLILINQEQYKAFFAILQKNTTPLMYNCTAGKDRTGLATALLLSALGVDNDTIIADYLLTNTFVNLSIDVVKDKYLLANNQQAEALMTLQTVKKEYLLKALETIKQHYGSVESYLTNQLAVDIPLMKQLYLY
>NZ_CP047050.1|WP_158209770.1|954321_955836_+|glutamate--tRNA-ligase
MANQVRVRFAPSPTGPLHIGGVRTALFNYLFAKKNNGVFYIRIEDTDQNRFVPGAEAYILEALEWLGISPDETIGKNEKFGPYRQSERKELYEQYANQLIANGWAYYAFDSAEDLDALRKQAESEGKTFIYNHSNREQLKTSLNLSKEEVDSLIANGEPFVIRFKTPVGETLELNDLIRGDIKFETSLLDDKVLYKSDGMPTYHLANIVDDHLMETSHVIRGEEWLPSLPLHELLYKAFGWEAPKFAHLPLILKPVGNGKLSKRDGDKLGFPVFPLDWVDPVSGEKSSGYREKGFYPETVINFLALLGWNDGTDQEIFSLAELVEKFDLNRVHKAGAKFDPEKNKWFNQHYLKLQENTDLADAYSVILTEKGIQAEKEYVTKVVSMIKERAIFVTDFYELSDFFFVAPTEYDAKALKNWKEDTSSIMMNVAEVIEGINDFDAKSIETEVKDWITKQEIGMGKVMQPLRLSLVGAVKGPDLFEIIEMIGKAETIKRIQTAVQKNA
>NZ_CP047050.1|WP_158209771.1|955969_956485_+|hypothetical-protein
MRRLSVLLLIGVFSLFYSCSNDDNSTGGKIEKEWIAFVQKHLIGDWTPKSIEVKPLVGAPVFSTPYPNQPNCKSDILRFEKNFTGTFNQNSSDCQLKINKFKWNHRLGELIFTLENGLEVKAVLLKKSANNLVFAIPVTEIMPVVEKLYPQIVNVDPVTLKLLHLKISLEK
>NZ_CP047050.1|WP_158209772.1|956559_957540_+|SPFH-domain-containing-protein
MTPTLIIVVVAVAILFLGFFTVKQQSAVIIERFGKFNSIRHSGLQLKIPLVDRISGVVNLRIQQLDVLIETKTKDNVFVKLKVSVQFKVIPDRVYDAFYKLEYPHDQITSYVFDVVRAEVPKLILDDVFERKDNIAVAVKAELNEAMTTYGYDIINTLITDIDPDIQVKNAMNRINAADREKVAAEYEAEASRIRIVAKAKAEAESKRLQGQGIADQRREIAQGLVESVDILNKVGINSQEASALIVVTQHYDTLQSVGSDSKSNLILLPNAPTVATDMLNTMVASFAASSKINEMTGSNVKTSDLSNKNYESKDLSNEMDYDEID
>NZ_CP047050.1|WP_158209773.1|957598_957844_-|hypothetical-protein
MRKAYTSFEEINQDLRILRVKRNLHYQKVFQSVDNIKDELTPDRLVRNTFGSVASYIKSSGNIQAFLITAALKFFFNRKRK
>NZ_CP047050.1|WP_090404629.1|957855_958206_-|phage-holin-family-protein
MAFEEIKDNIDDIKVDSEEFLRSSMNYYRLWGFKVTAKAGSIFMTLLLVGLFIMIAVLFFSLSAAFAIGECLDSRPIGFLIVGVVYLLITLLAYLFRKQLVEKPLIKKLSEIIFND
>NZ_CP047050.1|WP_158209774.1|958221_958563_-|YtxH-domain-containing-protein
MSDRLGNTVVALLAGAVVGAGLGILFAPAEGKKTRKKIKKTFDDSKDDLNDKIDELKKQVRDTVSKKKHDLEEGLEGFMSTTGKKRDEVISTLEKKLAELKTQANEAVENAKK
>NZ_CP047050.1|WP_158209775.1|958671_960354_-|glutamine--tRNA-ligase/YqeY-domain-fusion-protein
MSTKEKSLNFIEQIIEEDLKNGLPTEKLHFRFPPEPNGYLHIGHASSICLNFGLGLKYNAPVNLRFDDTNPSKEEQEFVDAIKHDVEWLGFEWANEVYASDYFQQLYDWTIQMIKDGKAYVDSQTSEVMAQQKGTPTTAGVDSPYRNRSVEENLDLFERMKNGEFEEGEHILRAKIDMAHKNMLMRDPIMYRIIKKSHHRTQNDWCIYPMYDWAHGESDYIESISHSFCTLEFLPHRELYDWFLDQVVVPENIRPKQREFARRNLSHTVVSKRKLARLVAEGHVTGWDDPRMSTISGLRRRGYTPISIRNYADTIGIAKRDNLIDVSLLEFCVREDLNKIAPRVMAVLDPVKLVITNYTEGQEEWLEAENNPEEEVMTYRKVPFSREIYIEREDFKEEANSKFFRLTLGKEVRLKNAYIIKGESVVKDEEGNILEIHATYDPESRSGSGTEASKRKVKGTIHWVSVPHAIEAEVRIYDRLFTDENPDGNKDVDFLDFVNPNSLEIVKGYLEPSLSTAKDGDKFQFQRLGYFCVDKESKENALVFNKTVGLRDTWNKIEQK
>NZ_CP047050.1|WP_090404638.1|960482_960839_+|dihydroneopterin-aldolase
MGIIKLNNIRTFSFHGCMDEEAKIGSDYRIDVVAKGDFTKAAATDELEYAIDYVHLNKIVKEEMDKRAKLLETVCQRIIDRVFVEIRMVNEVKVSVSKINPPIGGDVEYVTVEMQGVR
>NZ_CP047050.1|WP_158209776.1|961101_961785_-|LysE-family-transporter
MIDDLITGISLGFFLSFMIGPVFFILIETSITRGFKAAIAFDTGVILADALFFAVAFFSSFRLINAIKDDPALFIFGGIIMLTYGIISFVRLKKVQVDTLQIAPPNLRRDYLNLFAKGFLLNFINVGVLGFWLAIIITLGPNMDMDTGRMFTFFGFTITAYFITDLFKITLAKQLRKKLTPENILKVKKISSIILIVFGLVIMIKGILPKSGNNSLNIPIKALEQTE
>NZ_CP047050.1|WP_158209777.1|961870_962545_-|DUF2807-domain-containing-protein
MKKLALLLALIVSPFIFAQKSSVLGDFNTMGVFDQIQLTLVPSDTQKIEIEGTNADNVNVVNKNGNLKIKMNFVKSLQGEGIKVTLFYKNLTEILADEGASIKTTAPIKATKLDVTAKNGATIVAEIDTERVDVKAGSGSVVKLSGKAAVQDIVSNSGAEIKNKKLLTNQTTVTVNAGGQADVYASELVDAKTRAGGSITIYGNPKNVTEKNVLGGTVKKVTNE

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Crispr_ID: NZ_CP047050_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP047050_2

1338137-1338283

Orphan

Consensus_repeat	Method
GTGGTCCCACCTGGGCTCGAACCAGGGACTTACTGATTATGAGTCAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP047050_2

>merge|NZ_CP047050|2|1338137-1338283|CRISPRCasFinder
GTGGTCCCACCTGGGCTCGAACCAGGGACTTACTGATTATGAGTCAGTTACTCTAACCAACTGAGTTATAGGACCGCTCATATGAGCGTAAAATTTCGTGGTGGTCCCACCTGGGCTCGAACCAGGGACTTGCTGATTATGAGTCAG

>NZ_CP047050|2|2|1338137-1338283|CRISPRCasFinder
GTGGTCCCACCTGGGCTCGAACCAGGGACTTACTGATTATGAGTCAG	TTACTCTAACCAACTGAGTTATAGGACCGCTCATATGAGCGTAAAATTTCGTG
GTGGTCCCACCTGGGCTCGAACCAGGGACTTGCTGATTATGAGTCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047050.1\|WP_158210048.1\|1337051_1337873_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_016650134.1\|1330446_1330848_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|378971
NZ_CP047050.1\|WP_158210055.1\|1346078_1347140_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158210056.1\|1347249_1348329_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158210057.1\|1348389_1349922_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158210042.1\|1331079_1331490_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP047050.1\|WP_158210043.1\|1331564_1332362_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158210045.1\|1332916_1333831_-\|relaxase/mobilization-nuclease-domain-containing-protein	unknown	unknown	gnl\|CDD\|367497
NZ_CP047050.1\|WP_158210058.1\|1350303_1351302_+\|2-hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240659
NZ_CP047050.1\|WP_158210049.1\|1338381_1338783_-\|methylmalonyl-CoA-epimerase	unknown	unknown	gnl\|CDD\|319912
NZ_CP047050.1\|WP_158210047.1\|1335331_1336573_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273716
NZ_CP047050.1\|WP_016650142.1\|1336672_1336960_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP047050.1\|WP_158210053.1\|1343219_1344998_+\|HSP90-family-protein	unknown	unknown	gnl\|CDD\|237603
NZ_CP047050.1\|WP_158210052.1\|1340697_1343220_+\|sel1-repeat-family-protein	unknown	unknown	gnl\|CDD\|223861
NZ_CP047050.1\|WP_158210046.1\|1333832_1334132_-\|mobilization-protein	unknown	unknown	gnl\|CDD\|184361
NZ_CP047050.1\|WP_158210051.1\|1339245_1340457_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|226957
NZ_CP047050.1\|WP_158210050.1\|1338851_1339244_+\|30S-ribosome-binding-factor-RbfA	unknown	unknown	gnl\|CDD\|376719
NZ_CP047050.1\|WP_158210054.1\|1344997_1346074_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_059050600.1\|1334230_1335139_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379044
NZ_CP047050.1\|WP_158210044.1\|1332383_1332914_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP047050.1\|WP_016650134.1\|1330446_1330848_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|378971	pfam12844, HTH_19, Helix-turn-helix domain. Members of this family contains a DNA-binding helix-turn-helix domain. This family contains many example antitoxins from bacterial toxin-antitoxin systems. These antitoxins are likely to be DNA-binding domains.	3.44532e-06
NZ_CP047050.1\|WP_158210052.1\|1340697_1343220_+\|sel1-repeat-family-protein	gnl\|CDD\|223861	COG0790, COG0790, FOG: TPR repeat, SEL1 subfamily [General function prediction only].	1.39399e-28
NZ_CP047050.1\|WP_158210042.1\|1331079_1331490_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	3.1281e-08
NZ_CP047050.1\|WP_158210045.1\|1332916_1333831_-\|relaxase/mobilization-nuclease-domain-containing-protein	gnl\|CDD\|367497	pfam03432, Relaxase, Relaxase/Mobilisation nuclease domain. Relaxases/mobilisation proteins are required for the horizontal transfer of genetic information contained on plasmids that occurs during bacterial conjugation. The relaxase, in conjunction with several auxiliary proteins, forms the relaxation complex or relaxosome. Relaxases nick duplex DNA in a specific manner by catalyzing trans-esterification.	1.08182e-12
NZ_CP047050.1\|WP_158210058.1\|1350303_1351302_+\|2-hydroxyacid-dehydrogenase	gnl\|CDD\|240659	cd12183, LDH_like_2, D-Lactate and related Dehydrogenases, NAD-binding and catalytic domains. D-Lactate dehydrogenase (LDH) catalyzes the interconversion of pyruvate and lactate, and is a member of the 2-hydroxyacid dehydrogenase family. LDH is homologous to D-2-hydroxyisocaproic acid dehydrogenase (D-HicDH) and shares the 2-domain structure of formate dehydrogenase. D-2-hydroxyisocaproate dehydrogenase-like (HicDH) proteins are NAD-dependent members of the hydroxycarboxylate dehydrogenase family, and share the Rossmann fold typical of many NAD binding proteins. HicDH from Lactobacillus casei forms a monomer and catalyzes the reaction R-CO-COO(-) + NADH + H+ to R-COH-COO(-) + NAD+. D-HicDH, like the structurally distinct L-HicDH, exhibits low side-chain R specificity, accepting a wide range of 2-oxocarboxylic acid side chains. 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.	0
NZ_CP047050.1\|WP_158210049.1\|1338381_1338783_-\|methylmalonyl-CoA-epimerase	gnl\|CDD\|319912	cd07249, MMCE, Methylmalonyl-CoA epimerase (MMCE). MMCE, also called methylmalonyl-CoA racemase (EC 5.1.99.1) interconverts (2R)-methylmalonyl-CoA and (2S)-methylmalonyl-CoA. MMCE has been found in bacteria, archaea, and in animals. In eukaryotes, MMCE is an essential enzyme in a pathway that converts propionyl-CoA to succinyl-CoA, and is important in the breakdown of odd-chain length fatty acids, branched-chain amino acids, and other metabolites. In bacteria, MMCE participates in the reverse pathway for propionate fermentation, glyoxylate regeneration, and the biosynthesis of polyketide antibiotics. MMCE is closely related to glyoxalase I and type I extradiol dioxygenases.	2.92953e-54
NZ_CP047050.1\|WP_158210047.1\|1335331_1336573_-\|hypothetical-protein	gnl\|CDD\|273716	TIGR01613, putative_primase, phage/plasmid primase, P4 family, C-terminal domain. This model represents a clade within a larger family of proteins from viruses of bacteria and animals. Members of this family are found in phage and plasmids of bacteria and archaea only. The model describes a domain of about 300 residues, found generally toward the protein C-terminus. [DNA metabolism, DNA replication, recombination, and repair, Mobile and extrachromosomal element functions, Prophage functions].	0.00175937
NZ_CP047050.1\|WP_016650142.1\|1336672_1336960_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	2.5239e-06
NZ_CP047050.1\|WP_158210053.1\|1343219_1344998_+\|HSP90-family-protein	gnl\|CDD\|237603	PRK14083, PRK14083, HSP90 family protein; Provisional.	0
NZ_CP047050.1\|WP_158210046.1\|1333832_1334132_-\|mobilization-protein	gnl\|CDD\|184361	PRK13877, PRK13877, conjugal transfer transcriptional regulator TraJ.	0.00228292
NZ_CP047050.1\|WP_158210051.1\|1339245_1340457_+\|FtsX-like-permease-family-protein	gnl\|CDD\|226957	COG4591, LolE, ABC-type transport system, involved in lipoprotein release, permease component [Cell envelope biogenesis, outer membrane].	2.5003e-37
NZ_CP047050.1\|WP_158210050.1\|1338851_1339244_+\|30S-ribosome-binding-factor-RbfA	gnl\|CDD\|376719	pfam02033, RBFA, Ribosome-binding factor A.	7.35527e-29
NZ_CP047050.1\|WP_059050600.1\|1334230_1335139_-\|hypothetical-protein	gnl\|CDD\|379044	pfam13155, Toprim_2, Toprim-like. This is a family or Toprim-like proteins.	1.59769e-14

>NZ_CP047050.1|WP_158210048.1|1337051_1337873_-|hypothetical-protein
MNTLIETPFFFFHQKLEKFSSITLSKKFTYIIAPLLPISSLIVSVALLPYFYNLSKWYILLPLSALIYSVLLLTAVINFLKGQNIFLISNLNLIYRQSFKSFQNSTEYLLSLPVEKIISIDTAPIEKEKKYNKDNVFTFNTTHDTIIKETLYQLKKEVINDDTTVEDFKRAILYCIIKHVGHIEPFIKLELQSQHCAMFLESFFIPFVQLFTLHKTTLKESCRYFQYATAESHSAINYDSINKKGRKLITNAHKETYAKILENVKSQLSKKTF
>NZ_CP047050.1|WP_016650142.1|1336672_1336960_-|helix-turn-helix-domain-containing-protein
MTTLKIIQELNEIKLMITKGNQFQKEIFTIKDLMAYTGFSDSTIHKLTSKNLIPHHKPTNGTLFFDRLEIIEWIKQYRVFTDEEVLSQFSKQLKR
>NZ_CP047050.1|WP_158210047.1|1335331_1336573_-|hypothetical-protein
MTTTATEYIRIGTDYYAIRKKNVNGKEIIVERKLWKKSEIITDFGKDMIKELPKFFGYKCEPSHINYAHFIGDYFNSYSPILYDIDTTSVLSLNSLREQIPITFYFLQHIFGNQYLLGIDYFKILLFYPEQILPIIVLVSRNRETGKTTFLNWIKEIFDKNAVFIKANAFTEKFNSEMDSKLLLLIEEVKSDNKDIVEAIKYISTAMYQSIEYKGQEKVEQKSFLKIIMTSNHEHNFLKIDKEETRFWVIKVPVIKKRSTEFYTKLIKEVPIFLNYLYRVPFTTEKKTRMWFTPELIHTEALHKLKHDLDLQNKNQVLDILDIIFNEFEIDELDTTPSDINALLNYYNRGHNISMREIQTILENIALVRSANSNNYERIKIEDNTLKRIIHKGKYYRILKDTLLNQMTDEKLL
>NZ_CP047050.1|WP_059050600.1|1334230_1335139_-|hypothetical-protein
MTYQEAKNISLISILDNIGIRQSKINNKEAWYYSPFRTENTPSFHVSVTKNVFYDFGDNTYKGNVLDFVMLYYKCDVKEALKILASNSFSFHQLPSKIDTCEKRKDYQITAIIPLRNKYLIHYIKQRGLCLKIVQKYCKEVHYTIGDKAYYAIGFQNELGGVELRNKYIQICLGSKSLSYIDNGSTTVFIFEAFIDFLSFLTLKPNLEYKFDYIILNSVSTLDNTLIKPPNNYLYKTLDNKVMFESKYKSIIACLDNDKAGDKATDKLLTAFPLTTKDARVRYKHYKDLNDYLLSINRDKLT
>NZ_CP047050.1|WP_158210046.1|1333832_1334132_-|mobilization-protein
MKREHKIEFRVTLTESLLIKNKADKIGCSVSEYLRSTALGYALSYKLTQDEIEVYKLLNKFADNFRRIGNLFKLGDTTGVKEATIETSNLIRDHLQKLK
>NZ_CP047050.1|WP_158210045.1|1332916_1333831_-|relaxase/mobilization-nuclease-domain-containing-protein
MIAKAKTCIGGTALFNYVINPNKGYELVRNNLSGETPKDMFLTMQILQNQNLRCKNNTISVVISPTIEDSKKMTDQDLNNLVHDFLVGLKLDPKNAQYIAFVHTEKEHKHIHILANRIDENTKALKDNYIGFQAQRIAHEIALKYGWISIRQENENKKEQVKANQKQVAQEIKKAHYLVLKEHPKNLQQYIDMMQIHQIEVKPSVNKQGNIQGYRFIHLPTNTNLKASEVDRNLKLNELFENNTPKRSDDLFHTVLFKDQDKQISFENWNTNTASLFSFLNSYGNYYEDYAPDITKKKKRTIRR
>NZ_CP047050.1|WP_158210044.1|1332383_1332914_-|hypothetical-protein
MAKHQPTLTELTELLFKQVVYLQETMKQNIAQQTELADKINSIEVKVNLSELRNLETKNREGLQNDFTAFQSKLIHSKEELLKVYRAISNKKMFYLIALNIFLLFTSGLSMYIAIDKSIDSSKHEKLIDDNKKADLELNHLNQFFKENPKNYEAYKKWENRSKKNVLNSSYLSNKN
>NZ_CP047050.1|WP_158210043.1|1331564_1332362_-|hypothetical-protein
MQHIKLKPTQLISIDYNISDITQNSSQDFSDSKKIEEEYVKSSNLSDQIGMDLMLFTENSIVFGFDYSYKSDKIFIPEINPTLIFFSNAIMSVKSAKQFRANLMKDSPSLMKKSQTEINPELFGHYFQLAVNCIINLQASLETFINRCIPDNYIILSNNNKPIRKPNIHDKIDLGITKIKGLDFEKQFPEDYKIVKELIGLRNRIIHLNPTKENTNTKYKNFYREIIDFDFDKGIFSIRTFINFYEPNLIEDCSCGNEYYYKLIY
>NZ_CP047050.1|WP_158210042.1|1331079_1331490_+|helix-turn-helix-domain-containing-protein
MTTVTRKHIGKNISRIREIKGMKQITLAELLGVSQQQVSIIENSESVEETKLESIAKILEVPVDVIKDYSDERVLNIINSTFHESPFYSNTVNYNPTFNPLDKLLEAYEENKKLYERLLEAEKEKIAYLEKLLSKK
>NZ_CP047050.1|WP_016650134.1|1330446_1330848_-|helix-turn-helix-transcriptional-regulator
MEHKIHQGRNIKRFREMLGIKQEVLAFDLGDNWTQKKISLLEKKEVIDNSLLQEISNKLAVPIEAIKNFDSKRALSIISNTHIDSPTQKYHYDTINPVTAIVQLHNEKIELYERILKEKDEMMNRLEKLIQSK
>NZ_CP047050.1|WP_158210049.1|1338381_1338783_-|methylmalonyl-CoA-epimerase
MKKIEHIGIAVKDLQASNALFEKLFGAPAYKEESVESEGVKTSFFMNGPNKIELLEATNPDSPIAKFLEKKGEGIHHIAFDVEDIEAEMKRLSDEGFIVLNEKPKKGADNKLVAFLHPKTTNGVLIELCQEIK
>NZ_CP047050.1|WP_158210050.1|1338851_1339244_+|30S-ribosome-binding-factor-RbfA
METNRQKKMGTLLQKDIVDILQGEVRKNGLSNLIISVSKVSITTDLSISRVYLSIFPSEKGPELLKAIQSNAPLIKHELAQRVKHQLRKVPDLVFYIDDSLEYIDQIDKALKGEENPIADRDLLVKRKKK
>NZ_CP047050.1|WP_158210051.1|1339245_1340457_+|FtsX-like-permease-family-protein
MKFSLYIAKRYAFSKSKSKAINVITAIASIGIVVSAMAMFIVLSVFSGLRSFSLSFVNDLDPDLKVYSEKGKSFIVEDKQILDLEDSGYFKGVAKVVEDRLLFSFKEKQTVSTIKGVDSDYSNVSDFESKVEYGNWLEADSDETVVGIGISAVLSMGLFDTENAFEALAMKPGKGVINNPEDAFIKKTLNPTGVYILQNDDLDDKYVFVDIDVARDLLFIPANEITNLELAIADNVSESKAISKVKEVLGENFIIKNRAQQNDGLYRMLNTENLVVYLIFVLVVIMALFTLVGAMIMIILEKQSNIKTLNELGTPLTDLRKIFLFQGMIICGLGSLIGVFLGVVFVLLQAHFQFISIREGMAYPVEFNLMNLVLVFVSIIFLGLIASLIASSRVNHNYLQANK
>NZ_CP047050.1|WP_158210052.1|1340697_1343220_+|sel1-repeat-family-protein
MRNSFNEYKSYVSDFAADSVSLTEQAKSFIEANDYNDPNQWYKAYAICLLAVKEAKSNEVIEELYIQLNEDSNCVHSSMSLNAEDYATWFTDVRELNNLFINQGFIRAYGFQYELFLNARFSYKDDEIAKGYLQKGYELGDDLCTCHVGYSKYYGNLGYEKNQDEGLQLLQNIVAKTKIAAGELFLLNIEFRNCNSPEEGWQVIEKYSDLLHNQKKGLYVLADYYLREEQDAKAAEVLEEGIANKSAYSAYLLGMMCCNGRFESLGYTVERGRDLLDYAFDYGIVYSGFVLAYSYLYPLNGGERDFKTAIALLEKTVAYDSNEALLELATIRLYNEEYKDVEKAIGYLDRAIENGFDRAMSEKAFVLLDSGEVESNVVEAKALLEEATKLGSDYAPYRLGIAYQNTEFEDEPNYEKALEYFELSAERNNGMGLEYAGRYNRYGYAGEPNTEKAIAYYQQGIEQHGSNYCKVELAMMLERGEGLDANAEEAQALYIDALNNEYFFAALRLGFMSEDGVVGEPNLEEARKYFQIAADNDIAEGVYHLARFYRYGIGGDKNEEMAFELFEKALELGFVDANVDIALFYEEGVNGGEPNYAKAFEYMLEGAEAGFSYAQYKVGVYYSYGYLEERNSEEGKKWFEKAVENGSPLGMLALGDYYLYGYGPDQEYEKSFEYYKMAEERDYISEGIGICYQFGFGVEKDDKKAFQAYKAAAERHYDAAMFRLGLCYYYGNGVDKDLVEAFYYLKTVADNSYMDAVSYVGTMLIKGEGTDKDPEYGVSYLIQAAEAGIDSAQYELANCYLKGEGVPQSDEQAMQWYQQAAENGNEDAQKIVGGPRKRRR
>NZ_CP047050.1|WP_158210053.1|1343219_1344998_+|HSP90-family-protein
MEDKKQYQFQVNMKGMIELLSEHIYSSPTVFIRELLQNGMDAVTVRKGIDEQFKGAINVTFEGDRLIFQDNGVGLTQEDVHQFLSVIGQSSKRGELADKDLIGKFGIGLLSCLVVSEAIVVESRSLYREESVRWTGRADGTYNVEMIDLLPEVGTKVILDAKKAWKSLFKKDEVKQNILFYGSALPIEVNLIENGEVDQILNGNPVWLDPESTKEELLAYGKEVFKTKFLDVFRLQSDAGELQGVAFIIPNKVNTTATKEHKIFLKRMYLCDQASNLLPEWTSFVRCVINANALQPTASRESLMNNTVLQETKKELSICFKDYLKSLSLTDIDTLEKIINIHHMFIKALAASDSEIMNLFEDYLPFETNQGMLAFGDIKESVDKIYFTPSLDDFRQIRRIAGSQKKLVINAAYSYETDLIEKIKRSHPELSIEKINPNDILEEFEDAVESEELIEKFVLEANKILKKHFCRAEVKRFEPKDTTAIYIANEDAIASKNIQSLSQTSNPFASTLHHFKKKEEVMPTLCFNQQSDLVTKIMHIDDPELFEALINVLYVQALMLGGYTINKKEMDTFNDALYQFMILGMSNFLPKF
>NZ_CP047050.1|WP_158210054.1|1344997_1346074_+|hypothetical-protein
MYRLQIQKLALEIEEHYSDYDRCIALLQQAIQIADKHNDLDWGVDLRSYLIRKESATSMCIHSPAAFAWILNVCDEYPEEFSDAEFLGLYEWMLGAVNCNTDIPLEHTQTVALDLERRLEKNGMSKRGLYFCLAEFAQNRGDVAKGCEYIDLAKLEPKEDDEDEVVEYDYSVERASIIGDFEEAIYLANQMELKKLSAFSLPFESYCAMTYFMARRGDSRASIYLEKAKEAFYKVEGVNSSMLFSMTRFIYTLHLLEDELLYSMFELVVDWQVGAEDFLQMAFSQHIAAVFVKGGTRELKISPKQPYYKQEGIYDLAVLAAYYYSIAESFSTKFDQRNGNNHCCTELKQLQEENQPKK
>NZ_CP047050.1|WP_158210055.1|1346078_1347140_+|hypothetical-protein
MSYNLEIQKILLKLDDLQNFSDRVKALKEAIAIADKHNDIDWGFDLRLDLIRQERNTSKCEESFPAFAWILNASDENDDYFDEADFLWEYKWMFCSAYRSSAIPMEQVLEIGEDLKRRLVKNGFSLRAYYNVMTGLSLHLRDYKKAQEYIDLADAEIIDDMTNCPACELDTKVETLLYQGFVEESLIKAQDLINKKLTCYSMPFQTFCCFAYWLEQAGDDRASIYFDKAMEEYHAHDQYDSSVGYSMGLLVAYMHKKNHPDTWSFFEKIADWQLGAEDLHIFNFAKYMAPLMKNGGKQRLELSSLLPYYQESGEYDLSELYVYFKDIAYDYANRFDQRNGNDNFKTEVDEMLT
>NZ_CP047050.1|WP_158210056.1|1347249_1348329_+|hypothetical-protein
MSYTLDIQKIVLKINETKVIADQLVLIKEAIAIADKHNDIDWGFDLRLLLINTENHTPRTSLSYPAFTWILNTSDSNEGYFEEKDFLYEYKWMYAISSGSTAITKEQLKEIGDDFHKRLLKNGYSSRGYYHILAIWYQHLREYDKAMEIVNLMGEELVDELSDNPPFEHAIKTYNLLAQGKFEEAKIAARDLFANRFEFIETAFETYMVFAYEHFIRGNVNEAREYFELAQCNMSVYDENDPITHFRSRIFYMYLSWQFGGEECWDVFEKFCIWENGADSHYSLIFTKHAMCLLKEGGTRKFNFPVSLPYYQESGEYDLKVLCNYFKDCAFDLVARFDNRNGNNNFTKEANRLFAIPRL
>NZ_CP047050.1|WP_158210057.1|1348389_1349922_-|hypothetical-protein
MIAKIQLKLNNDVLLTVIKMVQQTDDYAVKNVTDALLISTKEDLITKLEEKAKNIHKQVSILDHNKKHSLVLKYHEAYSLYKLLDAVFNKQLFNDSPHIKRIKRLINELHNKVDIFAKEEDFAVVDVEHNDEVTTPAIATNLVETELFVNETTDQQVEITLEPAAFESLNFNEGVTDETHLNLFTEAPQENISPINSNSRSQTDVDTEEEQEAIIWEETLELDNLPIQEEIDKDLFSIEFTNENTIPKMDWEIIKAEDSIPSDCPPSPAAIEKQSLNDSKFSEFFNIAKKGINAEENDLAQKETKPSFQNKTTLFEIPATELPLVDNKPQEDITAIEQPLVIEDNLAIESEATLFEIPATELPLVDNKPQEDITAIEQPLVIEDNLAIENEATLFEIPVTELPLVDDKPQEDITTIEQPLVAEDNLAIESEATLFEIPATELPLVDDKPQEEITSEVGTQNTPNTKDVMQIEIFDVETIVTEPIVNKPKKERKKEKKNSSFDQEGQISLF
>NZ_CP047050.1|WP_158210058.1|1350303_1351302_+|2-hydroxyacid-dehydrogenase
MKIAFFSAQPYDITFFNKENKSFGFELEYFDTGLEEQTVNLITEGTDTVCVFVNDKVDAEVIKKLAKKNVKYIALRCAGFNNVDLEEAHKHNIKVCRVPAYSPEAVAEHTLALLFTLNRKIHKAYNRVREQNYSLNGLLGTNIYKKTVGIVGTGNIGAVFCRMMKALGTEVLAYDIYENEELKKEGIKYVSLDEIYAKSDIISLHCPLTPDTMHLINENTIAKMKDGVFLINTSRGKLIESHAAIQALRAKKIGALAIDVYEQEEKVFFRDLSETILEDERLQLLTSFPNVIVTAHQAFFTDEALSQISYITLDNLKQLSTKGAIEGRVAEL

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Crispr_ID: NZ_CP047050_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP047050_3

2144058-2150326

TypeI-B

I-A,II-B,III-A

Consensus_repeat	Method
CTTCTAATTGTACCTTGATGGAATTGAAAT	PILER-CR
CTTCTAATTGTACCTTGATGGAATTGAAAT	CRISPRCasFinder
CTTCTAATTGTACCTTGATGGAATTGAAAT	CRT

95 spacers

cas2,cas1,cas4,cas3,cas5,cas7b,cas8b1,cas6

The CRISPR arrays of NZ_CP047050_3

>merge|NZ_CP047050|3|2144058-2150326|PILER-CR,CRISPRCasFinder,CRT
CTTCTAATTGTACCTTGATGGAATTGAAATTGCTATCAATAGCGTGGTTAATGTATTTCATAATAACTTCTAATTGTACCTTGATGGAATTGAAATCCGTTTGAAGTTTTCGAAACTGAGCTATATAGCTTAGCTTCTAATTGTACCTTGATGGAATTGAAATAACTGGACAAATTAAAAGCGATTTAATCGGTTATACTTCTAATTGTACCTTGATGGAATTGAAATATTGTCAAATGTTGGTAAGTTAAGAGTTGAGGCAAACTTCTAATTGTACCTTGATGGAATTGAAATAATCGTATAGAATATGTATTCATTTTTTTTTTTTTACTTCTAATTGTACCTTGATGGAATTGAAATCGAAGTCGAATTAAGAGAATTTAAGTCTGCCAGCTGCTTCTAATTGTACCTTGATGGAATTGAAATGAAGAGAAAAAAGATGACACCTTATTGTATATAGGTCTTCTAATTGTACCTTGATGGAATTGAAATGCGAGATAGAGAATTCCATTCTATGTGCGAATTTTCTTCTAATTGTACCTTGATGGAATTGAAATCGGTAGAGTAACAGAAAACTTTACAAAGAAGTATGACTTCTAATTGTACCTTGATGGAATTGAAATAAGGATCTGGATAAAACGGATATTGATCGAGGGGGCTTCTAATTGTACCTTGATGGAATTGAAATTTGGATAGAAAGATCCTAAATGTATTAAAATACGACTTCTAATTGTACCTTGATGGAATTGAAATAGGAGTACAACTTGAATTATTTTAAATATAAATCTTCTTCTAATTGTACCTTGATGGAATTGAAATGCAACAGGCTGAAACCTCTCTACAGCCCTTGTCTCCTTCTAATTGTACCTTGATGGAATTGAAATGAAATTGCAGAATCTAAAAGACGTGATGCAGAATCTTCTAATTGTACCTTGATGGAATTGAAATACCCAAGAGACTTCTTCAATGTACCTGGCTCTATAAACTTCTAATTGTACCTTGATGGAATTGAAATAAAATAAGCATTAACAACGGTATAGAATGGTACTGTGCTTCTAATTGTACCTTGATGGAATTGAAATAGGGAATAGCAAGTTTACTAAACTTAACAATTATACACTTCTAATTGTACCTTGATGGAATTGAAATACAATATGAATAGGAGCTTTGTTTACATCTCCACGCTTCTAATTGTACCTTGATGGAATTGAAATATAACATACCTCGAGGTTATGGCATTTGGATAGTATCTTCTAATTGTACCTTGATGGAATTGAAATGATAGTGCTAAAAAAGCAATGGAAGAAGCTAAAACTTCTAATTGTACCTTGATGGAATTGAAATTGGTAAGCTGCAACAACACTATCTATCTTCCCACTTCTTCTAATTGTACCTTGATGGAATTGAAATGTAGTGGAATTGCGAAGAACATTAAAAGCGCAAAAGCTTCTAATTGTACCTTGATGGAATTGAAATCGGCTAATTGGCAAATCTATTTTTAGACTATTTTCTCTTCTAATTGTACCTTGATGGAATTGAAATGTAATTAAGTATGCTGCACATAATTTAGGAGTAAACCTTCTAATTGTACCTTGATGGAATTGAAATACAATAAATGATTCAGCTTTATGAACTTTAATAAGCTTCTAATTGTACCTTGATGGAATTGAAATTAGTCTGAGAACTTAGGTAAAGCAACATTACCTGTTCTTCTAATTGTACCTTGATGGAATTGAAATGTAATTAAGTATGCTGCACATAATTTAGGAGTAAACCTTCTAATTGTACCTTGATGGAATTGAAATAAGTTCACGGATATGGGTCAGTTTGGTTTTAGCTCTCTTCTAATTGTACCTTGATGGAATTGAAATAAGTATTAATCAAGAAGTTAAACATTAATAATTATCTTCTAATTGTACCTTGATGGAATTGAAATTCGAATCAATAGCGTGGTTAATATATTTCATATCAACTTCTAATTGTACCTTGATGGAATTGAAATACGGGTAAAGCAAGTGTTAGTGACGCTGATAATGCTTCTAATTGTACCTTGATGGAATTGAAATGATTTCTATAAACCTTTAGAGGGATACACGGAAATGCTTCTAATTGTACCTTGATGGAATTGAAATAAAGAATATGAGTTAGAAGAACGTTCTAACGAATTTCTTCTAATTGTACCTTGATGGAATTGAAATTAAACATTAACAAGGCTAAACCTCCTAAAACAAACACTTCTAATTGTACCTTGATGGAATTGAAATCAAGCAAGATTTGACGCTGAAATGGGGCGTTTACACTTCTAATTGTACCTTGATGGAATTGAAATATTACATTAACAACTCCAAAAGGAATTTTAATAAACTTCTAATTGTACCTTGATGGAATTGAAATTTACTTGTAAAACGTCCGACATAACCGCTGGCGCCCTTCTAATTGTACCTTGATGGAATTGAAATATTTAAAGAGTCCATTTCCAGAAGCGAAACCAAAAGCTTCTAATTGTACCTTGATGGAATTGAAATAGGAGGAATTCCACCAAACTTGGTTTCAGGGGGCAGCTTCTAATTGTACCTTGATGGAATTGAAATATACCTACCGTTGCGCCACCAGCGACCGCCAACGGCTTCTAATTGTACCTTGATGGAATTGAAATATATACTCACGTGTCGCCTGACAAGCTGAGTCGTAAACTTCTAATTGTACCTTGATGGAATTGAAATTAACTTGCAAATTCACCATTTGAAGTCTTTGCAACTTCTAATTGTACCTTGATGGAATTGAAATTAACTAATATCAAAAGCAAATGCGATAGATACGAAACTTCTAATTGTACCTTGATGGAATTGAAATACACCTACCGCGCCACCACCAGCGATGGCTAACGGACTTCTAATTGTACCTTGATGGAATTGAAATAAGCAAAAATCAAAGAAAGAAGAAGATAATCAACCTTCTAATTGTACCTTGATGGAATTGAAATATATTTATGTTTGAGCTCTTTGCTCTTGATGTATCTTCTAATTGTACCTTGATGGAATTGAAATTAATATAGGTAATGTCTTAGTATCATCTTTTCAGCGTCTTCTAATTGTACCTTGATGGAATTGAAATCTATAGTGTGGGAGGTTTTCTTTATCTATAACATACTTCTAATTGTACCTTGATGGAATTGAAATTTTTAAATATTACTTAATGATCCTACTTTCTTTTTCTTCTAATTGTACCTTGATGGAATTGAAATAGGATTGTCTTTAAATCAAGCCTTAGAGCAAATTAACTTCTAATTGTACCTTGATGGAATTGAAATTGTGTTATTGCTTGTTGTTTTCTCCAAAATCCACGACTTCTAATTGTACCTTGATGGAATTGAAATTTATATGTTAGCAAGAAAACAGAGTCTGTCAAGTATCTTCTAATTGTACCTTGATGGAATTGAAATGGAATTGGAGTACTTGCAATTGTTGCTACTTGTGCTTCTAATTGTACCTTGATGGAATTGAAATTATATATCCAAAATATGTTTATACAATTGTATAGGAACTTCTAATTGTACCTTGATGGAATTGAAATACAAATCGTTTTATATCTATGCTTTGATTCATTGCACTTCTAATTGTACCTTGATGGAATTGAAATAACGCTATGTACGCATCTTGTTTGTGAGCAACACTCTTCTAATTGTACCTTGATGGAATTGAAATGCATTAAAAGACTCTAATAGAGTATCTTTCCTACTCCTTCTAATTGTACCTTGATGGAATTGAAATTTGTAATAAAAATAGTTTCTAATTAAACACTAAAAGCTTCTAATTGTACCTTGATGGAATTGAAATTTTCTAAGTGCAAATGCAGCATCCTTTACGCTGTTACTTCTAATTGTACCTTGATGGAATTGAAATAAATTAATTTCAACTCCTTTTGTTTTTTCTACAAATCTTCTAATTGTACCTTGATGGAATTGAAATTAAGTTATTCCTTTGTATTCTATTTTGAGTACGTAAACTTCTAATTGTACCTTGATGGAATTGAAATTAATGTACAAATGTGTTGTAAAGGAATAAGCCTCCGCTTCTAATTGTACCTTGATGGAATTGAAATGGCTGAAAACCTGCTGTTTAGCGGTAATCAAATTAGGCTTCTAATTGTACCTTGATGGAATTGAAATGCAAATCTGAAAAAGGCGCCCCTAATGGTATTGCTTCCTTCTAATTGTACCTTGATGGAATTGAAATAAAAGTAACATCTGAAAACTACGAATTAACATATAGCTTCTAATTGTACCTTGATGGAATTGAAATTAAATAGTGTCCGTTTTTAAATCGTGATAAACATTCTTCTAATTGTACCTTGATGGAATTGAAATCCTTTAATAACAATAAAAAACTGTAAAAAAGTATTCTTCTAATTGTACCTTGATGGAATTGAAATAAAAAATATCTAAATGATCCGTATTTTTTAAAGAACTTCTAATTGTACCTTGATGGAATTGAAATCTCCATCAGTTCCATCAGGTCTAACGCTTTCAGATTCTTCTAATTGTACCTTGATGGAATTGAAATCACATCGAGTGAAATTCTCTGTCTCCTTGATAAAAGCTTCTAATTGTACCTTGATGGAATTGAAATGCTAATCTCTCATCTGGTTTATCCATAAGTCTTTATTCTTCTAATTGTACCTTGATGGAATTGAAATCAAAGAAGTACGAACCTTTAAAGAAGTACAATACTAACTTCTAATTGTACCTTGATGGAATTGAAATAATAGTCGTGTATCGAGATTAGAAAATTCTAAAACGCTTCTAATTGTACCTTGATGGAATTGAAATAAAAGGATAGGCTTAGTTCCTGAACTTAAAATTTCTCTTCTAATTGTACCTTGATGGAATTGAAATTCGTGATGAGCCAGCTGAGTAGAGCAGTTGAAACGCCTTCTAATTGTACCTTGATGGAATTGAAATTCTTGTGTGATGCTAAAATCAACTTCAGAGAAATCTCTTCTAATTGTACCTTGATGGAATTGAAATTCGCATATTTTGAGGGCACAAGCTGATATACATTAACTTCTAATTGTACCTTGATGGAATTGAAATCGGTTTGCTCGTCTAAACTCTTGTACCGAGTTAACTTCTAATTGTACCTTGATGGAATTGAAATAAGAATTAACGACCTTCAAAAACAAGAATTAGAAGTCTTCTAATTGTACCTTGATGGAATTGAAATCTAATGCTTAAAACGTCTTGTAATCCTTGTATAGCTTCTAATTGTACCTTGATGGAATTGAAATATGAGAAGGTATTGATGCGAGGGGATTCTGAGGCACCTTCTAATTGTACCTTGATGGAATTGAAATTCCACTCCTCCAGCTCGTCCAAAATTTCGTTTTACTTCTAATTGTACCTTAATGGAATTGAAATTCCGACGTCCTTTGAATTAGCATAATCTCAATATCGCTTCTAATTGTACCTTAATGGAATTGAAATTTTAGTTCGTGCTTATCACTTTTATAAGCGTCCTTCTTCTAATTGTACCTTAATGGAATTGAAATATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGTCTTCTAATTGTACCATAATGGAATTGAAATATACTGGATCTCTTAAACGTGTACATTCGTTTTACTTCTAATTGTACCTTAATGGAATTGAAATATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGTCTTCTAATTGTACCATAATGGAATTGAAATATACTGGATCTCTTAAACGTGTACATTCGTTTTACTTCTAATTGTACCTTAATGGAATTGAAATATACACGCTTCAATTCTTTCTTTACTCGCTTGCTGCTTCTAATTGTACCTTAATGGAATTGAAATTACTCATCCTCTCCGTATCCTTCCTCATTGTTATGTCTTCTAATTGTACCTTAATGGAATTGAAATAGAAATATGGCTATTACAATTGAGCAGAGAATGACGCTTCTAATTGTACCTTGATGGAATTGAAATTTAGACCATACTTTTTGAACGTCAAATTCACGAGGACTTCTAATTGTACCTTGATGGAATTGAAATTTGCTATAAATCTCGTAGTATTTGTAAAATTTTCGATCTTCTAATTGTACCTTGATGGAATTGAAATTTGTAAATACAATAAGGTAGTTCGTTAAAACCAAGAACTTCTAATTGTACCTTGATGGAATTGAAATAATGCTACTAAAACACCGTTTAAATCGTATTTAAACTTCTAATTGTATCTTGATGGAATTGTAAG

>NZ_CP047050|3|1|2144058-2150261|PILER-CR
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGCTATCAATAGCGTGGTTAATGTATTTCATAATAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCGTTTGAAGTTTTCGAAACTGAGCTATATAGCTTAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACTGGACAAATTAAAAGCGATTTAATCGGTTATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTGTCAAATGTTGGTAAGTTAAGAGTTGAGGCAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATCGTATAGAATATGTATTCATTTTTTTTTTTTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGAAGTCGAATTAAGAGAATTTAAGTCTGCCAGCTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAGAGAAAAAAGATGACACCTTATTGTATATAGGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCGAGATAGAGAATTCCATTCTATGTGCGAATTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTAGAGTAACAGAAAACTTTACAAAGAAGTATGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGGATCTGGATAAAACGGATATTGATCGAGGGGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGGATAGAAAGATCCTAAATGTATTAAAATACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGTACAACTTGAATTATTTTAAATATAAATCTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAACAGGCTGAAACCTCTCTACAGCCCTTGTCTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAATTGCAGAATCTAAAAGACGTGATGCAGAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACCCAAGAGACTTCTTCAATGTACCTGGCTCTATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAATAAGCATTAACAACGGTATAGAATGGTACTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGGAATAGCAAGTTTACTAAACTTAACAATTATACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATATGAATAGGAGCTTTGTTTACATCTCCACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATAACATACCTCGAGGTTATGGCATTTGGATAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATAGTGCTAAAAAAGCAATGGAAGAAGCTAAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGGTAAGCTGCAACAACACTATCTATCTTCCCACTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAGTGGAATTGCGAAGAACATTAAAAGCGCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGCTAATTGGCAAATCTATTTTTAGACTATTTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATAAATGATTCAGCTTTATGAACTTTAATAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAGTCTGAGAACTTAGGTAAAGCAACATTACCTGTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTTCACGGATATGGGTCAGTTTGGTTTTAGCTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTATTAATCAAGAAGTTAAACATTAATAATTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGAATCAATAGCGTGGTTAATATATTTCATATCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACGGGTAAAGCAAGTGTTAGTGACGCTGATAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATTTCTATAAACCTTTAGAGGGATACACGGAAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAGAATATGAGTTAGAAGAACGTTCTAACGAATTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAACATTAACAAGGCTAAACCTCCTAAAACAAACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAGCAAGATTTGACGCTGAAATGGGGCGTTTACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTACATTAACAACTCCAAAAGGAATTTTAATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTACTTGTAAAACGTCCGACATAACCGCTGGCGCC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTTAAAGAGTCCATTTCCAGAAGCGAAACCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGGAATTCCACCAAACTTGGTTTCAGGGGGCAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATACCTACCGTTGCGCCACCAGCGACCGCCAACGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATACTCACGTGTCGCCTGACAAGCTGAGTCGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTTGCAAATTCACCATTTGAAGTCTTTGCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTAATATCAAAAGCAAATGCGATAGATACGAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACACCTACCGCGCCACCACCAGCGATGGCTAACGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGCAAAAATCAAAGAAAGAAGAAGATAATCAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATTTATGTTTGAGCTCTTTGCTCTTGATGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATATAGGTAATGTCTTAGTATCATCTTTTCAGCGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTATAGTGTGGGAGGTTTTCTTTATCTATAACATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTTAAATATTACTTAATGATCCTACTTTCTTTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGATTGTCTTTAAATCAAGCCTTAGAGCAAATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGTGTTATTGCTTGTTGTTTTCTCCAAAATCCACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTATATGTTAGCAAGAAAACAGAGTCTGTCAAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGAATTGGAGTACTTGCAATTGTTGCTACTTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TATATATCCAAAATATGTTTATACAATTGTATAGGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAAATCGTTTTATATCTATGCTTTGATTCATTGCA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACGCTATGTACGCATCTTGTTTGTGAGCAACACT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCATTAAAAGACTCTAATAGAGTATCTTTCCTACTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAATAAAAATAGTTTCTAATTAAACACTAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTCTAAGTGCAAATGCAGCATCCTTTACGCTGTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAATTAATTTCAACTCCTTTTGTTTTTTCTACAAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAGTTATTCCTTTGTATTCTATTTTGAGTACGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATGTACAAATGTGTTGTAAAGGAATAAGCCTCCG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGCTGAAAACCTGCTGTTTAGCGGTAATCAAATTAGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAAATCTGAAAAAGGCGCCCCTAATGGTATTGCTTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGTAACATCTGAAAACTACGAATTAACATATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAATAGTGTCCGTTTTTAAATCGTGATAAACATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCTTTAATAACAATAAAAAACTGTAAAAAAGTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAAATATCTAAATGATCCGTATTTTTTAAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTCCATCAGTTCCATCAGGTCTAACGCTTTCAGATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CACATCGAGTGAAATTCTCTGTCTCCTTGATAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCTAATCTCTCATCTGGTTTATCCATAAGTCTTTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAAGAAGTACGAACCTTTAAAGAAGTACAATACTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATAGTCGTGTATCGAGATTAGAAAATTCTAAAACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGGATAGGCTTAGTTCCTGAACTTAAAATTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGTGATGAGCCAGCTGAGTAGAGCAGTTGAAACGC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCTTGTGTGATGCTAAAATCAACTTCAGAGAAATCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGCATATTTTGAGGGCACAAGCTGATATACATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTTTGCTCGTCTAAACTCTTGTACCGAGTTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGAATTAACGACCTTCAAAAACAAGAATTAGAAGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTAATGCTTAAAACGTCTTGTAATCCTTGTATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATGAGAAGGTATTGATGCGAGGGGATTCTGAGGCAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCCACTCCTCCAGCTCGTCCAAAATTTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	TCCGACGTCCTTTGAATTAGCATAATCTCAATATCG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TTTAGTTCGTGCTTATCACTTTTATAAGCGTCCTT
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATACACGCTTCAATTCTTTCTTTACTCGCTTGCTG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TACTCATCCTCTCCGTATCCTTCCTCATTGTTATGT
CTTCTAATTGTACCTTAATGGAATTGAAAT	AGAAATATGGCTATTACAATTGAGCAGAGAATGACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTAGACCATACTTTTTGAACGTCAAATTCACGAGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGCTATAAATCTCGTAGTATTTGTAAAATTTTCGAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAAATACAATAAGGTAGTTCGTTAAAACCAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT

>NZ_CP047050|3|3|2144058-2150326|CRISPRCasFinder
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGCTATCAATAGCGTGGTTAATGTATTTCATAATAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCGTTTGAAGTTTTCGAAACTGAGCTATATAGCTTAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACTGGACAAATTAAAAGCGATTTAATCGGTTATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTGTCAAATGTTGGTAAGTTAAGAGTTGAGGCAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATCGTATAGAATATGTATTCATTTTTTTTTTTTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGAAGTCGAATTAAGAGAATTTAAGTCTGCCAGCTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAGAGAAAAAAGATGACACCTTATTGTATATAGGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCGAGATAGAGAATTCCATTCTATGTGCGAATTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTAGAGTAACAGAAAACTTTACAAAGAAGTATGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGGATCTGGATAAAACGGATATTGATCGAGGGGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGGATAGAAAGATCCTAAATGTATTAAAATACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGTACAACTTGAATTATTTTAAATATAAATCTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAACAGGCTGAAACCTCTCTACAGCCCTTGTCTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAATTGCAGAATCTAAAAGACGTGATGCAGAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACCCAAGAGACTTCTTCAATGTACCTGGCTCTATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAATAAGCATTAACAACGGTATAGAATGGTACTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGGAATAGCAAGTTTACTAAACTTAACAATTATACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATATGAATAGGAGCTTTGTTTACATCTCCACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATAACATACCTCGAGGTTATGGCATTTGGATAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATAGTGCTAAAAAAGCAATGGAAGAAGCTAAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGGTAAGCTGCAACAACACTATCTATCTTCCCACTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAGTGGAATTGCGAAGAACATTAAAAGCGCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGCTAATTGGCAAATCTATTTTTAGACTATTTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATAAATGATTCAGCTTTATGAACTTTAATAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAGTCTGAGAACTTAGGTAAAGCAACATTACCTGTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTTCACGGATATGGGTCAGTTTGGTTTTAGCTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTATTAATCAAGAAGTTAAACATTAATAATTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGAATCAATAGCGTGGTTAATATATTTCATATCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACGGGTAAAGCAAGTGTTAGTGACGCTGATAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATTTCTATAAACCTTTAGAGGGATACACGGAAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAGAATATGAGTTAGAAGAACGTTCTAACGAATTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAACATTAACAAGGCTAAACCTCCTAAAACAAACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAGCAAGATTTGACGCTGAAATGGGGCGTTTACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTACATTAACAACTCCAAAAGGAATTTTAATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTACTTGTAAAACGTCCGACATAACCGCTGGCGCC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTTAAAGAGTCCATTTCCAGAAGCGAAACCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGGAATTCCACCAAACTTGGTTTCAGGGGGCAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATACCTACCGTTGCGCCACCAGCGACCGCCAACGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATACTCACGTGTCGCCTGACAAGCTGAGTCGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTTGCAAATTCACCATTTGAAGTCTTTGCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTAATATCAAAAGCAAATGCGATAGATACGAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACACCTACCGCGCCACCACCAGCGATGGCTAACGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGCAAAAATCAAAGAAAGAAGAAGATAATCAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATTTATGTTTGAGCTCTTTGCTCTTGATGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATATAGGTAATGTCTTAGTATCATCTTTTCAGCGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTATAGTGTGGGAGGTTTTCTTTATCTATAACATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTTAAATATTACTTAATGATCCTACTTTCTTTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGATTGTCTTTAAATCAAGCCTTAGAGCAAATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGTGTTATTGCTTGTTGTTTTCTCCAAAATCCACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTATATGTTAGCAAGAAAACAGAGTCTGTCAAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGAATTGGAGTACTTGCAATTGTTGCTACTTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TATATATCCAAAATATGTTTATACAATTGTATAGGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAAATCGTTTTATATCTATGCTTTGATTCATTGCA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACGCTATGTACGCATCTTGTTTGTGAGCAACACT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCATTAAAAGACTCTAATAGAGTATCTTTCCTACTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAATAAAAATAGTTTCTAATTAAACACTAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTCTAAGTGCAAATGCAGCATCCTTTACGCTGTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAATTAATTTCAACTCCTTTTGTTTTTTCTACAAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAGTTATTCCTTTGTATTCTATTTTGAGTACGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATGTACAAATGTGTTGTAAAGGAATAAGCCTCCG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGCTGAAAACCTGCTGTTTAGCGGTAATCAAATTAGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAAATCTGAAAAAGGCGCCCCTAATGGTATTGCTTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGTAACATCTGAAAACTACGAATTAACATATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAATAGTGTCCGTTTTTAAATCGTGATAAACATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCTTTAATAACAATAAAAAACTGTAAAAAAGTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAAATATCTAAATGATCCGTATTTTTTAAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTCCATCAGTTCCATCAGGTCTAACGCTTTCAGATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CACATCGAGTGAAATTCTCTGTCTCCTTGATAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCTAATCTCTCATCTGGTTTATCCATAAGTCTTTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAAGAAGTACGAACCTTTAAAGAAGTACAATACTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATAGTCGTGTATCGAGATTAGAAAATTCTAAAACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGGATAGGCTTAGTTCCTGAACTTAAAATTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGTGATGAGCCAGCTGAGTAGAGCAGTTGAAACGC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCTTGTGTGATGCTAAAATCAACTTCAGAGAAATCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGCATATTTTGAGGGCACAAGCTGATATACATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTTTGCTCGTCTAAACTCTTGTACCGAGTTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGAATTAACGACCTTCAAAAACAAGAATTAGAAGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTAATGCTTAAAACGTCTTGTAATCCTTGTATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATGAGAAGGTATTGATGCGAGGGGATTCTGAGGCAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCCACTCCTCCAGCTCGTCCAAAATTTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	TCCGACGTCCTTTGAATTAGCATAATCTCAATATCG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TTTAGTTCGTGCTTATCACTTTTATAAGCGTCCTT
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATACACGCTTCAATTCTTTCTTTACTCGCTTGCTG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TACTCATCCTCTCCGTATCCTTCCTCATTGTTATGT
CTTCTAATTGTACCTTAATGGAATTGAAAT	AGAAATATGGCTATTACAATTGAGCAGAGAATGACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTAGACCATACTTTTTGAACGTCAAATTCACGAGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGCTATAAATCTCGTAGTATTTGTAAAATTTTCGAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAAATACAATAAGGTAGTTCGTTAAAACCAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATGCTACTAAAACACCGTTTAAATCGTATTTAAA
CTTCTAATTGTATCTTGATGGAATTGTAAG

>NZ_CP047050|3|1|2144058-2150326|CRT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGCTATCAATAGCGTGGTTAATGTATTTCATAATAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCGTTTGAAGTTTTCGAAACTGAGCTATATAGCTTAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACTGGACAAATTAAAAGCGATTTAATCGGTTATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTGTCAAATGTTGGTAAGTTAAGAGTTGAGGCAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATCGTATAGAATATGTATTCATTTTTTTTTTTTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGAAGTCGAATTAAGAGAATTTAAGTCTGCCAGCTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAGAGAAAAAAGATGACACCTTATTGTATATAGGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCGAGATAGAGAATTCCATTCTATGTGCGAATTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTAGAGTAACAGAAAACTTTACAAAGAAGTATGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGGATCTGGATAAAACGGATATTGATCGAGGGGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGGATAGAAAGATCCTAAATGTATTAAAATACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGTACAACTTGAATTATTTTAAATATAAATCTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAACAGGCTGAAACCTCTCTACAGCCCTTGTCTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	GAAATTGCAGAATCTAAAAGACGTGATGCAGAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACCCAAGAGACTTCTTCAATGTACCTGGCTCTATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAATAAGCATTAACAACGGTATAGAATGGTACTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGGAATAGCAAGTTTACTAAACTTAACAATTATACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATATGAATAGGAGCTTTGTTTACATCTCCACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATAACATACCTCGAGGTTATGGCATTTGGATAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATAGTGCTAAAAAAGCAATGGAAGAAGCTAAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGGTAAGCTGCAACAACACTATCTATCTTCCCACTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAGTGGAATTGCGAAGAACATTAAAAGCGCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGCTAATTGGCAAATCTATTTTTAGACTATTTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAATAAATGATTCAGCTTTATGAACTTTAATAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAGTCTGAGAACTTAGGTAAAGCAACATTACCTGTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GTAATTAAGTATGCTGCACATAATTTAGGAGTAAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTTCACGGATATGGGTCAGTTTGGTTTTAGCTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGTATTAATCAAGAAGTTAAACATTAATAATTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGAATCAATAGCGTGGTTAATATATTTCATATCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACGGGTAAAGCAAGTGTTAGTGACGCTGATAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GATTTCTATAAACCTTTAGAGGGATACACGGAAATG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAGAATATGAGTTAGAAGAACGTTCTAACGAATTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAACATTAACAAGGCTAAACCTCCTAAAACAAACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAGCAAGATTTGACGCTGAAATGGGGCGTTTACA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTACATTAACAACTCCAAAAGGAATTTTAATAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTACTTGTAAAACGTCCGACATAACCGCTGGCGCC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATTTAAAGAGTCCATTTCCAGAAGCGAAACCAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGAGGAATTCCACCAAACTTGGTTTCAGGGGGCAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATACCTACCGTTGCGCCACCAGCGACCGCCAACGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATACTCACGTGTCGCCTGACAAGCTGAGTCGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTTGCAAATTCACCATTTGAAGTCTTTGCAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAACTAATATCAAAAGCAAATGCGATAGATACGAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACACCTACCGCGCCACCACCAGCGATGGCTAACGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGCAAAAATCAAAGAAAGAAGAAGATAATCAAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATATTTATGTTTGAGCTCTTTGCTCTTGATGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATATAGGTAATGTCTTAGTATCATCTTTTCAGCGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTATAGTGTGGGAGGTTTTCTTTATCTATAACATA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTTAAATATTACTTAATGATCCTACTTTCTTTTT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AGGATTGTCTTTAAATCAAGCCTTAGAGCAAATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TGTGTTATTGCTTGTTGTTTTCTCCAAAATCCACGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTATATGTTAGCAAGAAAACAGAGTCTGTCAAGTAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGAATTGGAGTACTTGCAATTGTTGCTACTTGTG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TATATATCCAAAATATGTTTATACAATTGTATAGGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	ACAAATCGTTTTATATCTATGCTTTGATTCATTGCA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AACGCTATGTACGCATCTTGTTTGTGAGCAACACT
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCATTAAAAGACTCTAATAGAGTATCTTTCCTACTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAATAAAAATAGTTTCTAATTAAACACTAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTTCTAAGTGCAAATGCAGCATCCTTTACGCTGTTA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAATTAATTTCAACTCCTTTTGTTTTTTCTACAAAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAGTTATTCCTTTGTATTCTATTTTGAGTACGTAAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAATGTACAAATGTGTTGTAAAGGAATAAGCCTCCG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GGCTGAAAACCTGCTGTTTAGCGGTAATCAAATTAGG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCAAATCTGAAAAAGGCGCCCCTAATGGTATTGCTTC
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGTAACATCTGAAAACTACGAATTAACATATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TAAATAGTGTCCGTTTTTAAATCGTGATAAACATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CCTTTAATAACAATAAAAAACTGTAAAAAAGTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAAATATCTAAATGATCCGTATTTTTTAAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTCCATCAGTTCCATCAGGTCTAACGCTTTCAGATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CACATCGAGTGAAATTCTCTGTCTCCTTGATAAAAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	GCTAATCTCTCATCTGGTTTATCCATAAGTCTTTATT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CAAAGAAGTACGAACCTTTAAAGAAGTACAATACTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATAGTCGTGTATCGAGATTAGAAAATTCTAAAACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAAAGGATAGGCTTAGTTCCTGAACTTAAAATTTCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGTGATGAGCCAGCTGAGTAGAGCAGTTGAAACGC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCTTGTGTGATGCTAAAATCAACTTCAGAGAAATCT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCGCATATTTTGAGGGCACAAGCTGATATACATTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	CGGTTTGCTCGTCTAAACTCTTGTACCGAGTTAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AAGAATTAACGACCTTCAAAAACAAGAATTAGAAGT
CTTCTAATTGTACCTTGATGGAATTGAAAT	CTAATGCTTAAAACGTCTTGTAATCCTTGTATAG
CTTCTAATTGTACCTTGATGGAATTGAAAT	ATGAGAAGGTATTGATGCGAGGGGATTCTGAGGCAC
CTTCTAATTGTACCTTGATGGAATTGAAAT	TCCACTCCTCCAGCTCGTCCAAAATTTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	TCCGACGTCCTTTGAATTAGCATAATCTCAATATCG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TTTAGTTCGTGCTTATCACTTTTATAAGCGTCCTT
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATAATTTCAGCAAGCTTATCGCGGTTAGCCTTTGGT
CTTCTAATTGTACCATAATGGAATTGAAAT	ATACTGGATCTCTTAAACGTGTACATTCGTTTTA
CTTCTAATTGTACCTTAATGGAATTGAAAT	ATACACGCTTCAATTCTTTCTTTACTCGCTTGCTG
CTTCTAATTGTACCTTAATGGAATTGAAAT	TACTCATCCTCTCCGTATCCTTCCTCATTGTTATGT
CTTCTAATTGTACCTTAATGGAATTGAAAT	AGAAATATGGCTATTACAATTGAGCAGAGAATGACG
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTAGACCATACTTTTTGAACGTCAAATTCACGAGGA
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGCTATAAATCTCGTAGTATTTGTAAAATTTTCGAT
CTTCTAATTGTACCTTGATGGAATTGAAAT	TTGTAAATACAATAAGGTAGTTCGTTAAAACCAAGAA
CTTCTAATTGTACCTTGATGGAATTGAAAT	AATGCTACTAAAACACCGTTTAAATCGTATTTAAA
CTTCTAATTGTATCTTGATGGAATTGTAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047050.1\|WP_158210607.1\|2143589_2143853_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP047050.1\|WP_158210609.1\|2153351_2153684_+\|killer-suppression-protein-HigA	unknown	unknown	gnl\|CDD\|226079
NZ_CP047050.1\|WP_158210601.1\|2135568_2137512_+\|hypothetical-protein	cas8b1	mkCas0106_cas8b1_CAS-I-B	unknown
NZ_CP047050.1\|WP_158210603.1\|2138498_2139269_+\|type-I-B-CRISPR-associated-protein-Cas5	cas5	cls001430_cas5_CAS-I-B	gnl\|CDD\|131641
NZ_CP047050.1\|WP_158210606.1\|2142580_2143588_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	gnl\|CDD\|274695
NZ_CP047050.1\|WP_158210600.1\|2134771_2135566_+\|CRISPR-associated-endoribonuclease-Cas6	cas6	COG1583_cas6_CAS-I:CAS-III:CAS-IV	gnl\|CDD\|224499
NZ_CP047050.1\|WP_090406322.1\|2132727_2133087_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378822
NZ_CP047050.1\|WP_158210612.1\|2157362_2158073_+\|hydrogenase-nickel-incorporation-protein-HypB	unknown	unknown	gnl\|CDD\|349775
NZ_CP047050.1\|WP_158210613.1\|2158080_2158563_+\|urease-accessory-protein-UreE	unknown	unknown	gnl\|CDD\|237322
NZ_CP047050.1\|WP_158210602.1\|2137514_2138438_+\|CRISPR-associated-protein	cas7b	pfam05107_cas7b_CAS-I-B:CAS-I-C	gnl\|CDD\|377458
NZ_CP047050.1\|WP_158210611.1\|2154871_2156098_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340882
NZ_CP047050.1\|WP_158210599.1\|2133463_2134096_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158210614.1\|2158552_2159557_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|223687
NZ_CP047050.1\|WP_090406290.1\|2157006_2157351_+\|hydrogenase-maturation-nickel-metallochaperone-HypA	unknown	unknown	gnl\|CDD\|376468
NZ_CP047050.1\|WP_158210604.1\|2139252_2142048_+\|CRISPR-associated-helicase-Cas3'	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP047050.1\|WP_090406278.1\|2159572_2160580_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376439
NZ_CP047050.1\|WP_158210605.1\|2142050_2142560_+\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
NZ_CP047050.1\|WP_158210610.1\|2153700_2154798_+\|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl\|CDD\|225635
NZ_CP047050.1\|WP_158210608.1\|2152086_2153112_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211364.1\|2151403_2151775_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319898

Protein	Function_ID	Function_description	E-value
NZ_CP047050.1\|WP_158210607.1\|2143589_2143853_+\|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.	3.25703e-28
NZ_CP047050.1\|WP_158210609.1\|2153351_2153684_+\|killer-suppression-protein-HigA	gnl\|CDD\|226079	COG3549, HigB, Plasmid maintenance system killer protein [General function prediction only].	1.79839e-10
NZ_CP047050.1\|WP_158210603.1\|2138498_2139269_+\|type-I-B-CRISPR-associated-protein-Cas5	gnl\|CDD\|131641	TIGR02592, hypothetical_protein_CTC_01466, CRISPR-associated protein Cas5, subtype I-B/HMARI. This is a CRISPR-associated protein unique to the hmari subtype of cas genes and CRISPR repeat, which is the only subtype present in Haloarcula marismortui ATCC 43049. The hmari type, though uncommon, is also found in the Aquificae, Thermotogae, Firmicutes, and Dictyoglomi.	5.95374e-23
NZ_CP047050.1\|WP_158210606.1\|2142580_2143588_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274695	TIGR03641, cas1_HMARI, CRISPR-associated endonuclease Cas1, subtype I-B/HMARI/TNEAP. 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 Cas1 subgroup that includes Cas1 proteins of the related HMARI and TNEAP subtypes of CRISPR/Cas system.	5.69792e-163
NZ_CP047050.1\|WP_158210600.1\|2134771_2135566_+\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|224499	COG1583, COG1583, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	2.40496e-19
NZ_CP047050.1\|WP_090406322.1\|2132727_2133087_+\|hypothetical-protein	gnl\|CDD\|378822	pfam12158, DUF3592, Protein of unknown function (DUF3592). This family of proteins is functionally uncharacterized.This family of proteins is found in bacteria, archaea, eukaryotes and viruses. Proteins in this family are typically between 150 and 242 amino acids in length.	0.00126877
NZ_CP047050.1\|WP_158210612.1\|2157362_2158073_+\|hydrogenase-nickel-incorporation-protein-HypB	gnl\|CDD\|349775	cd05390, HypB, nickel incorporation protein HypB. HypB is one of numerous accessory proteins required for the maturation of nickel-dependent hydrogenases, like carbon monoxide dehydrogenase or urease. HypB is a GTP-binding protein and has GTP hyrolase activity. It forms homodimer and is capable of binding two nickel ions and two zinc ions. The active site is located on the dimer interface. Energy from hydrolysis of GTP is used to insert nickels into hydrogenases.	3.42909e-93
NZ_CP047050.1\|WP_158210613.1\|2158080_2158563_+\|urease-accessory-protein-UreE	gnl\|CDD\|237322	PRK13261, ureE, urease accessory protein UreE; Provisional.	5.41956e-10
NZ_CP047050.1\|WP_158210602.1\|2137514_2138438_+\|CRISPR-associated-protein	gnl\|CDD\|377458	pfam05107, Cas_Cas7, CRISPR-associated protein Cas7. CRISPR-associated protein Cas7 is one of the components of the type I-B cascade-like antiviral defense complex. In Haloferax volcanii, Cas5, Cas6 and Cas7 form a small complex that aids the stability of CRISPR-derived RNA.	1.03274e-42
NZ_CP047050.1\|WP_158210611.1\|2154871_2156098_-\|MFS-transporter	gnl\|CDD\|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.88947e-51
NZ_CP047050.1\|WP_158210614.1\|2158552_2159557_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|223687	COG0614, FepB, ABC-type Fe3+-hydroxamate transport system, periplasmic component [Inorganic ion transport and metabolism].	5.21157e-45
NZ_CP047050.1\|WP_158210604.1\|2139252_2142048_+\|CRISPR-associated-helicase-Cas3'	gnl\|CDD\|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	4.74252e-31
NZ_CP047050.1\|WP_090406278.1\|2159572_2160580_+\|iron-ABC-transporter-permease	gnl\|CDD\|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	3.20641e-76
NZ_CP047050.1\|WP_158210605.1\|2142050_2142560_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	1.27139e-52
NZ_CP047050.1\|WP_158211364.1\|2151403_2151775_+\|VOC-family-protein	gnl\|CDD\|319898	cd06587, VOC, vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC is found in a variety of structurally related metalloproteins, including the type I extradiol dioxygenases, glyoxalase I and a group of antibiotic resistance proteins. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). Type I extradiol dioxygenases catalyze the incorporation of both atoms of molecular oxygen into aromatic substrates, which results in the cleavage of aromatic rings. They are key enzymes in the degradation of aromatic compounds. Type I extradiol dioxygenases include class I and class II enzymes. Class I and II enzymes show sequence similarity; the two-domain class II enzymes evolved from a class I enzyme through gene duplication. Glyoxylase I catalyzes the glutathione-dependent inactivation of toxic methylglyoxal, requiring zinc or nickel ions for activity. The antibiotic resistance proteins in this family use a variety of mechanisms to block the function of antibiotics. Bleomycin resistance protein (BLMA) sequesters bleomycin's activity by directly binding to it. Whereas, three types of fosfomycin resistance proteins employ different mechanisms to render fosfomycin inactive by modifying the fosfomycin molecule. Although the proteins in this superfamily are functionally distinct, their structures are similar. The difference among the three dimensional structures of the three types of proteins in this superfamily is interesting from an evolutionary perspective. Both glyoxalase I and BLMA show domain swapping between subunits. However, there is no domain swapping for type 1 extradiol dioxygenases.	4.64925e-05
NZ_CP047050.1\|WP_090406290.1\|2157006_2157351_+\|hydrogenase-maturation-nickel-metallochaperone-HypA	gnl\|CDD\|376468	pfam01155, HypA, Hydrogenase/urease nickel incorporation, metallochaperone, hypA. HypA is a metallochaperone that binds nickel to bring it safely to its target. The targets for Hypa are the nickel-containing enzymes [Ni,Fe]-hydrogenase and urease. The nickel coordinates with four nitrogens within the protein. The four conserved cysteines towards the C-terminus bind one zinc moiety probably to stabilize the protein fold.	9.36772e-23
NZ_CP047050.1\|WP_158210610.1\|2153700_2154798_+\|ImmA/IrrE-family-metallo-endopeptidase	gnl\|CDD\|225635	COG3093, VapI, Plasmid maintenance system antidote protein [General function prediction only].	2.56513e-10

>NZ_CP047050.1|WP_158210607.1|2143589_2143853_+|CRISPR-associated-endonuclease-Cas2
MYVILVYDISDKKVGKMLKLCRRYLNWIQNSVFEGEISEVKLKELLSEAKLFMDKDKDSVIVFKSREEKWLEKVVIGREKNDLDTFL
>NZ_CP047050.1|WP_158210606.1|2142580_2143588_+|type-I-B-CRISPR-associated-endonuclease-Cas1
MKKTYYLFNAGRLSRKDNTLKFVAVDQNGVEAPAKYIPVEGVSDLFCFGSLDANSSLYNFLGKAGIAVHFFDYYEHYTGSFSPKEYLLAGKMQIEQTRQYIDKKKRLVLARKFVSGATFNITKNLKYYINREKDLSEILYNIEHLTLSINNTSEIDELMGIEGNIRQMYYKAFDEIISTDFTMGNRTKRPPENEINALISYGNMLCYTLCLSQIYHTQLNPTISFLHEPGYRRYSLALDLAEIFKPLLVDRLIFRLLNKKEIQAKDFDHQLNSCLLKESGRKIFTRVWEERINETFKHPVLNRHVSYKHLIKLECYKLSKHILGIEEYKPFKARW
>NZ_CP047050.1|WP_158210605.1|2142050_2142560_+|CRISPR-associated-protein-Cas4
MLINATHINLYHVCKRELWLHYNGIRMEYNSELVADGKLIGETSYSDRSSKYTELQLGNVKIDFYDAKNKIVHEVKRSDKVEHAHLAQVKYYLYRLLLAGVRDATGILEYPTLRQREEVLLTNNDISEIRKWEQEIESICTSEVCPSVINAKICKSCSYQDFCYIQEAD
>NZ_CP047050.1|WP_158210604.1|2139252_2142048_+|CRISPR-associated-helicase-Cas3'
MSNSYKTVKELLSEVPSLRSFLLNEETYWAHRPKERDSAKRPETLHEHVELVNTYFEKLVNIHQIDEGIDSLIQKYLQDVNVTNLELGNEIKKQFVNSIVFHDYGKVNEAFQADKDKMDNPEFYGKERANSPIATNHSALGAFIYLAKHFNDIFDKFKDNQPYLLLSTAFFFSYSIFKHHSPKIDDNVDITLYMAYIMANKDKKEVIDFMSSYFKEFQYDINPVVLQYIGDKKVLERYVFKTFCKSASLYALVKMNFSLLTASDYLATNEYSSELSTTDFGVFSQERIDELYDNVSKHKYLDSAGTKLNYNAKTYEDLDTCDLKNPIEMSGGNLNILRKEMGVEVLRNIRNNLDKNLFYIEAPTGGGKTNLSILATIELLKGHNGKLNKVFYVFPFTTLITQTFGTLKEVLGLKEDEIVELHSRSGFSEKEEHDGQYGKDKLNYISNLFAHYPVSLLSHISFFDILKTNRKEKNYLFHRLANSIVVLDELQSYSPSHWDKLIYFIRFYAATLNIKFILMSATLPKLDKLLVLKEDVKDFVYLIPEARAKYFQNLNFSGRVDFDFDYFERTDLKLPELADRLVSESKTFAELDYGSAKPYGSVYTIIEFIYKQSASEFYEILKTDDFFDEIFVLSGTILEHRRQYIINFLKNKDNRFKKVLLITTQVVEAGVDIDMDLGFKDRSLIDSDEQLAGRINRNVNKKNCKLFLFNYNKESAIYGNDIRLKITREQIKAPVYKQILETKDFDKLYDLVINNRNNWNDQVMAVNFGEYESHVKKLKFTKVHEEFKLIDSNNISCFLPVDIAIEIGDEDNKISFFKESELAFLAKHQIYPTINGEIKGAEVFDLYLDIIQNRIDFTEQRIREKILQSIMSKYIISIFATENIERQLIHFSDLDKSRFGYQYISHWKEFYSVEGGMDNLKFKGVEETQFL
>NZ_CP047050.1|WP_158210603.1|2138498_2139269_+|type-I-B-CRISPR-associated-protein-Cas5
MKLVSIDLHSEFGFFRKPDTNNTINLSYNMIHKPAVLGILGAILGLGGYKEKGVLPEYYVQLKDLKIAIEPLNHDKGNFVKTAIKYTNTVGYANKGSNYLTEELTLVKPSYRIYLLLNESDILQGKLLKYLSEAQTEFIPYFGKNEFTAWWTKSSFKEYSFELANGDLEEGIELKSLFLKTIIHKDNSEVPFPAFGSSDIDLDSFVYFERLPMNFNEELMQYELFDFAYSSYLIKNSKALDNLYCLKETETYVQFI
>NZ_CP047050.1|WP_158210602.1|2137514_2138438_+|CRISPR-associated-protein
MSTTFKNRVYGAAVIKSINSNYNADFSGQPRKLPNGVVYATDKALKYSVRNYWKTALNENIFYFKSLNETMAPRSLDETYLLHYKEFKHEKDKDKSKLRLEVLGNLLKNLDVRLFGGTYAGKTNISIHGTCQITHGVNKFSENVIYSEQIMSPFRNSNEGSAENTMTTLGSQSRLEEGHYVHHFSVNPKNIEEDVNRVEAKGLTSDDIDKLKEGLRKGATYYDSAAKSGTENELLLWVELKENAKTVLPSFVNLIDINDNKEIDLSKVQALLKEPHIASDIQKIELYYSKALTKVINLPEGAVVSEM
>NZ_CP047050.1|WP_158210601.1|2135568_2137512_+|hypothetical-protein
MIKELVNFTQALPEEFKNQGSQPKEGLHILLHQKNENQVCSIDLVDFEYELFSKKEKEEVSAFLNKCKTLQQNAWCIDTNKCFDLPTKAIHSCSPYMVAFKREHLIGGEKYKANAGGKKKQIYERFSGYFEKTSLLFENETEKEVNKIVEHFFTQNQFSLILDKIEMRLESDRVLLLGKQEELKELFQKSNDKAEKQKCKDALSVIDQELLKVRQLTDADYIIFYIDESIENYKKVHKKYLDDKLFNTDKYNTIPNEEGLIYGTSNFLNGFNSNMPFLMHQTASFDISGRISNLEAKFLYEFKNILPNKILPSPLPVFIYQEELDDLMIKIIRENGFKLGYKEIIEKLIKDYSADASNYYLLFWQNTKDGIVFKDFDFVTKFEYKLKDEMQIENFFEIKEKGGKDLKFYPLITNVFELEQTVLKPFIQTRFLRVDYFSDLSKDGYEGLDLTFVSYSKYRKTVYDYVYKSQRQTIDQHMFDEMVFNAVKDDIKRVNEYGIKEKLNIWYSTQHFFNQQNKEYMGSKLKDYQNFVEEVISDEGLLREANDTDFAFISGMVIDYLMSKSKSADTSYQLLEPYLQQSKCSEFKKAIANDFARYKHENYSRSFERAAAFVLSYETTINLKQLLPEILSGVFAKNQLYSKIKNQ
>NZ_CP047050.1|WP_158210600.1|2134771_2135566_+|CRISPR-associated-endoribonuclease-Cas6
MRFKLILEAIEGTLVIPVNYQYPLSSAIYRIIAKGDKEYASFLHERGYGKGYKFFSFSDIKCPFTIQGDRLHLKQNTLEFQIAFQLPEAMQHFVQGLFASEKICIADKKSKQSFKVKSIETIPNLFSSKTLNEILSIEVKPFSPLVVGEKNERRHYDYLSPEDLRFLDSFIMNWREKIKAFYDLETANTALLMIEPKFYLKGSRPRLITIKDNTEAETKIKGYINFKIAITAERRFVDLLLNVGGGLYNAQGMGFLEVIDEKKI
>NZ_CP047050.1|WP_158210599.1|2133463_2134096_-|hypothetical-protein
MARIPNSILGEFTGSIGTVIGYNYRGQKCMRTKPKKSNYKSTPAQLKQQQKFKLSHEFLYPLSDVTDLYFGHKIGAKSRTNLALSHLLLYAIKDIDDNLQIDYQQVVITKGYLPAATITEVTLTDEELRINWTPNGGRDLALDSDKAKVVLFCEKQKLFFLPDKEGIRSEGTFTSPLPENWKAKNCIVWFFFAKQDDSECSTSVNFYGLI
>NZ_CP047050.1|WP_090406322.1|2132727_2133087_+|hypothetical-protein
MQSNLAKIIFLVLVVAGGIGAYMLYNGGMFDTRKYKSEYVTYAKSEATIVDIEEVKRRKSNELTWTLEYKDYAGNLKKERIAGESFMRKKVGDKIVIYYDSVANRLAVTEQRYKEIMRD
>NZ_CP047050.1|WP_158211364.1|2151403_2151775_+|VOC-family-protein
MKLGAFSVSLTVKDIHVSKAFYEKLGFYQRGGDITQNWVVMKNGDTIVGLFQGMFDANMLTFNPGWNQEAQNIDDFVDVRDIQKHLLAQGVELHTKADESTQGPAYVILVDPDGNPILIDQHR
>NZ_CP047050.1|WP_158210608.1|2152086_2153112_+|hypothetical-protein
MKRIKGIIVLGALCCLPFGTVFAQEKRSDMKEEKVFYDEDDKRLYKRILKDEKGKVIEVEDNGFMIDGKPQKMYKGVYKEGKPFEGYFKEEKILSEINLINYYEQGERKAQYSYDYLARDQFAAPFMYDLETVYEGGKVKSGRVYKEVEEGNALGIVNYENFEEKSLFIDLFEMHYFNRISFELTDDQLSIKDMSGESLIVVKKAGNKLTADYFIKGQHLFTAKPFIEVVKKGSPLSMTVYYKDKKEVEQEFSFKRLPFDSNMDQFANQFLTPIFLQFPAVYEGSLEQLLSAITSKFDVIAKDLNAIESFADLLPFSVYPFDEKKIVGVEEYDEKGQLVKE
>NZ_CP047050.1|WP_158210609.1|2153351_2153684_+|killer-suppression-protein-HigA
MNISFKTKKLQKIANDDKAMKKELGGIRAQKFQLRLQQILAADTLEDLRYASGKYHELTGDRKGQWACSLDGPYRLIFEPYEDPIPSDENGRYLWVEIKEVEMIEIVDYH
>NZ_CP047050.1|WP_158210610.1|2153700_2154798_+|ImmA/IrrE-family-metallo-endopeptidase
MKTKHTYSPQTVLHPGIDLTEKLEEIEMGTKEFAVRTNKPEKTINAVLKGESSITPEMAVLFENVLHIPANYWLNRQRNYDEYLARLSAQQTLKKASDWARSFPLNELIKCGWIEDLKPIEERANALLSFFGFSNIEAWGAYYYERQLKVAFRISLHGTKNPYALSAWLRQGELEAKKLQVPVYNEKLLKSNLTRFKEIMVKQSASFFEELQQLCGECGVALVLIPCIKGTQISGASRWVNDTPVVQMSGRHNRYDIFWFTFFHELGHILLHGKKDIFLEEITYSDADMIKEAEADSFAVKHLLTDIQVEKVVKDKPYTKDKFLKYANEFQTHSSIIVGRLKKLKAIEQFEFSELIIPFSNKNEE
>NZ_CP047050.1|WP_158210611.1|2154871_2156098_-|MFS-transporter
MTEPQNNAFTGYQKFAIFILAITQFTVILDFMVMAPLGDLLLKSLDMNTKDFSIAVSAYAFSAGIAGLLTAGFADRFDRKKLLLFFYVGFIIGTLFCALANSYTTLVLARIVTGLFGGVIGSISMAIITDLFSLQQRGRVMGFVQMGFGASQVLGIPIGLYIANKWYWEAPFFMIVGLSILIAFAIAIYFKPVTEHLKLQQNKKVVAHLWHTLKHKDYRIGFLSICFLSVGGFMLMPFGTIFAVNNLGVHPDQLPILFMISGISSLALMPFIGKLSDRMDKYRLFTIASIWLMTVSVVYTNLFQIPFWLVVTTNILMMIGIMSRMVPATALSSAIPYSKDRGAYMSISSSIQQISGGIAATISGLIVYQESATSPLINYDKVAYMVIIVSCISIFLMGRINRLVQQNR
>NZ_CP047050.1|WP_090406290.1|2157006_2157351_+|hydrogenase-maturation-nickel-metallochaperone-HypA
MHELTIVKDIFSTLEEHYQAKSEDIVKIEITAGLLSNVQPVLIQNAFDAFIADNETYKDMELDVVVQDIIAHCDSCNKDFKVEFHKFVCPCGQPSSNIVQGNDLFISKVIFKQA
>NZ_CP047050.1|WP_158210612.1|2157362_2158073_+|hydrogenase-nickel-incorporation-protein-HypB
MANNPKSLGNRVGSLQCDNTTLHLLKANDYVANAIREKLKNVCVINVCSSPGSGKTTLMQETGKRLANEINISVLVGDPETDRDAVRMQEVGINALQIVTGGMCHIEAQMILQALDHIDLSETDLLFIENVGNLLCPSAFDLGEDYRVTLLATTEGDDKPKKYPRMFLTSELMVVSKADLLPYVPFTVENVTKDAREVNPNIEVLTISTLKGDGMDQWCQWLKDKVAEKKAKNTEE
>NZ_CP047050.1|WP_158210613.1|2158080_2158563_+|urease-accessory-protein-UreE
MQEVILIDEVLSAEVGCSNEVADVFEIEWFETQKQLIKRQTKQGVELHLTKTVNRDWQQGDLLCANGVCLAKIAVKPALCIVFSSDVEREVADFCYYIGNRHLPLFTDADKKSFTVPYDGNLYEQLLAKLNDKISLQEKTLLMQNEVKHVRKLIKLSNEK
>NZ_CP047050.1|WP_158210614.1|2158552_2159557_+|ABC-transporter-substrate-binding-protein
MKNKQFLFFALVMISAVFTNACKSKVEEKEQVQETSVTALDCRDKEITLDAVAQRIVVLYDPLVDDIYMLGAQDKLVGIPQQVYQKEDTFSFLSKLDKRIANKEIATPSFGGGSSNIESIIGLQPDLVITFDKDIETVEQLEQLGIKVYTVSSKSQEVIYKELIGMATLLGKKERAEEIVTYIRAEVAKMQTAKFENPKTAYYAWSKGRVLSTSGKGTLMDLAINLSGAVNACPLEMEAPNVGAETLYKWNPDIIILWDSSQNDVYSLKELENLPAVKNKHVYEMYPTFYYDPHTVKFLLFAKQVRNWCYNEKSADELNVEIQEVLKELYKTNN
>NZ_CP047050.1|WP_090406278.1|2159572_2160580_+|iron-ABC-transporter-permease
MGNKLKVALLWVVPIVLVIGSLLLGSTENLSLSELLHYAGRMFARWQGQDIATSPIETILWKVRMPRIILTFLVGASLASAGGVLQAIFRNPIVDPFTLGISSGAAFGAALAMLFPFMSINLSAFAFGVCAVLMTYGVSYAGSRTSIVSMVLSGIIISGIFTALLTLLQYLSDPYKLQAIIQWTMGNLHTASWSKVNMAVYPIVIGLAVIVFLRWKLNLLSLGDNEALAVGVNPKVLKLVLIAVSTMITASSVAAVGVISLFGLIVPHISRMIFGPDNSICVWANISIGGAFLLVIDDFSRAIMPFEIPVGVFTMLIGAPIFIYLMKKSLMNWNG

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Crispr_ID: NZ_CP047050_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP047050_4

3060537-3060641

Orphan

Consensus_repeat	Method
ATCTCCTTTGTCTCCTTTTGGTCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP047050_4

>merge|NZ_CP047050|4|3060537-3060641|CRISPRCasFinder
ATCTCCTTTGTCTCCTTTTGGTCCTTTTAAACCGTCTAACTGTTCTTCTGTAAAGTCCTCATAAACAAATGAATACCCATCATCTCCTTTGTCTCCTTTTGGACC

>NZ_CP047050|4|4|3060537-3060641|CRISPRCasFinder
ATCTCCTTTGTCTCCTTTTGGTCC	TTTTAAACCGTCTAACTGTTCTTCTGTAAAGTCCTCATAAACAAATGAATACCCATC
ATCTCCTTTGTCTCCTTTTGGACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047050.1\|WP_158211267.1\|3061825_3062719_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211266.1\|3056487_3058164_-\|gamma-glutamyltransferase	unknown	unknown	gnl\|CDD\|223482
NZ_CP047050.1\|WP_158211259.1\|3045850_3047974_+\|dipeptidyl-carboxypeptidase-II	unknown	unknown	gnl\|CDD\|341051
NZ_CP047050.1\|WP_158211268.1\|3062715_3063615_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211262.1\|3052879_3053056_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211261.1\|3052292_3052820_+\|NADPH-dependent-FMN-reductase	unknown	unknown	gnl\|CDD\|377026
NZ_CP047050.1\|WP_158211272.1\|3069110_3069749_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211265.1\|3054931_3055948_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211263.1\|3053067_3053415_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211258.1\|3043655_3045641_-\|S8-family-serine-peptidase	unknown	unknown	gnl\|CDD\|173791
NZ_CP047050.1\|WP_158211275.1\|3080054_3081092_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP047050.1\|WP_158211271.1\|3066890_3067823_-\|type-IX-secretion-system-membrane-protein-PorP/SprF	unknown	unknown	gnl\|CDD\|371704
NZ_CP047050.1\|WP_158211264.1\|3053754_3054873_+\|FUSC-family-protein	unknown	unknown	gnl\|CDD\|379231
NZ_CP047050.1\|WP_158211386.1\|3067834_3069088_-\|gliding-motility-associated-C-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|372639
NZ_CP047050.1\|WP_158211260.1\|3048076_3051898_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211274.1\|3072109_3078508_-\|DUF11-domain-containing-protein	unknown	unknown	gnl\|CDD\|275067
NZ_CP047050.1\|WP_158211385.1\|3058289_3059561_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|189968
NZ_CP047050.1\|WP_158211273.1\|3069848_3072074_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP047050.1\|WP_158211270.1\|3064903_3066874_-\|OmpA-family-protein	unknown	unknown	gnl\|CDD\|143586
NZ_CP047050.1\|WP_158211269.1\|3063620_3064508_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP047050.1\|WP_158211275.1\|3080054_3081092_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.29386e-15
NZ_CP047050.1\|WP_158211266.1\|3056487_3058164_-\|gamma-glutamyltransferase	gnl\|CDD\|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP047050.1\|WP_158211259.1\|3045850_3047974_+\|dipeptidyl-carboxypeptidase-II	gnl\|CDD\|341051	cd06456, M3A_DCP, Peptidase family M3, dipeptidyl carboxypeptidase (DCP). Peptidase family M3 dipeptidyl carboxypeptidase (DCP; Dcp II; peptidyl dipeptidase; EC 3.4.15.5). This metal-binding M3A family also includes oligopeptidase A (OpdA; EC 3.4.24.70). DCP cleaves dipeptides off the C-termini of various peptides and proteins, the smallest substrate being N-blocked tripeptides and unblocked tetrapeptides. DCP from Escherichia coli is inhibited by the anti-hypertensive drug captopril, an inhibitor of the mammalian angiotensin converting enzyme (ACE, also called peptidyl dipeptidase A). OpdA may play a specific role in the degradation of signal peptides after they are released from precursor forms of secreted proteins. It can also cleave N-acetyl-L-Ala. This family also includes Arabidopsis thaliana organellar oligopeptidase OOP (At5g65620), which plays a role in targeting peptide degradation in mitochondria and chloroplasts; it degrades peptide substrates that are between 8 to 23 amino acid residues, and shows a weak preference for hydrophobic residues (F/L) at the P1 position.	0
NZ_CP047050.1\|WP_158211386.1\|3067834_3069088_-\|gliding-motility-associated-C-terminal-domain-containing-protein	gnl\|CDD\|372639	pfam13585, CHU_C, C-terminal domain of CHU protein family. The function of this C-terminal domain is not known; there are several conserved tryptophan and asparagine residues.	4.99752e-26
NZ_CP047050.1\|WP_158211261.1\|3052292_3052820_+\|NADPH-dependent-FMN-reductase	gnl\|CDD\|377026	pfam03358, FMN_red, NADPH-dependent FMN reductase.	3.62586e-35
NZ_CP047050.1\|WP_158211264.1\|3053754_3054873_+\|FUSC-family-protein	gnl\|CDD\|379231	pfam13515, FUSC_2, Fusaric acid resistance protein-like.	5.68177e-21
NZ_CP047050.1\|WP_158211385.1\|3058289_3059561_-\|hypothetical-protein	gnl\|CDD\|189968	pfam01391, Collagen, Collagen triple helix repeat (20 copies). Members of this family belong to the collagen superfamily. Collagens are generally extracellular structural proteins involved in formation of connective tissue structure. The alignment contains 20 copies of the G-X-Y repeat that forms a triple helix. The first position of the repeat is glycine, the second and third positions can be any residue but are frequently proline and hydroxy-proline. Collagens are post translationally modified by proline hydroxylase to form the hydroxy-proline residues. Defective hydroxylation is the cause of scurvy. Some members of the collagen superfamily are not involved in connective tissue structure but share the same triple helical structure. The family includes bacterial collagen-like triple-helix repeat proteins.	2.80837e-07
NZ_CP047050.1\|WP_158211274.1\|3072109_3078508_-\|DUF11-domain-containing-protein	gnl\|CDD\|275067	TIGR04226, Fimbrial_subunit_type_2, fimbrial isopeptide formation D2 domain. The Streptococcus Pneumoniae pilus backbone protein, RrgB, has three tandem domains with Lys-to-Asn isopeptide bonds, but these three regions are extremely divergent in sequence. This model represents the homology domain family of the D2 domain. It occurs just once in many surface proteins but up to twenty times in some pilin subunit proteins. Three of every four members have the typical Gram-positive C-terminal motif, LPXTG, although in many cases this motif may be involved in pilin subunit cross-linking rather than cell wall attachment. Proteins with this domain include fimbrial proteins with lectin-like adhesion functions, and the majority of characterized members are involved in surface adhesion to host structures.	8.13446e-06
NZ_CP047050.1\|WP_158211258.1\|3043655_3045641_-\|S8-family-serine-peptidase	gnl\|CDD\|173791	cd04842, Peptidases_S8_Kp43_protease, Peptidase S8 family domain in Kp43 proteases. Kp43 proteases are members of the peptidase S8 or Subtilase clan of proteases. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure (an example of convergent evolution). Kp43 is topologically similar to kexin and furin both of which are proprotein convertases, but differ in amino acids sequence and the position of its C-terminal barrel. Kp43 has 3 Ca2+ binding sites that differ from the corresponding sites in the other known subtilisin-like proteases. KP-43 protease is known to be an oxidation-resistant protease when compared with the other subtilisin-like proteases.	1.20046e-47
NZ_CP047050.1\|WP_158211270.1\|3064903_3066874_-\|OmpA-family-protein	gnl\|CDD\|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	1.11686e-37
NZ_CP047050.1\|WP_158211271.1\|3066890_3067823_-\|type-IX-secretion-system-membrane-protein-PorP/SprF	gnl\|CDD\|371704	pfam11751, PorP_SprF, Type IX secretion system membrane protein PorP/SprF. This entry describes a protein family unique to, and greatly expanded in, the Bacteriodetes. Species in this lineage include several, such as Cytophaga hutchinsonii and Cytophaga johnsonae (Flavobacterium johnsoniae), that exhibit a poorly understood rapid gliding phenotype. Several members of this protein family are found in operons with other genes whose loss leads to a loss of the rapid gliding phenotype.	6.03633e-104

>NZ_CP047050.1|WP_158211385.1|3058289_3059561_-|hypothetical-protein
MYDETTNSWTKINGDNGEAGAKGDQGIQGPVGPQGPKGETGDQGIQGDKGLSVTAKPGEDGSVIIIDGEGTEHIVSKGDQGIQGPVGPQGPKGETGDQGIQGDKGLSVTAKPGEDGSVIIIDGEGTEHIVSKGDQGIQGPVGPQGAKGDTGATGPAGANGKDGEKGDTGAKGDTGVTGAQGPAGVGGVTTVVLPLKINGKNGTMNDVGTASNPYVISINTAVFEAPGVVKPVDTDFKLLTDGTLSIKPGFKNGAWNKQKAPNDRPETTEDDIYQYGNVAIGADNVPAKLGNIATNAKLYVEGDTFVNGTIYSQTSTYADYVFEKYFLGESAIKYDYDFKDLEYVKNFVKENHHLPGVTPIGDLNKAANGYIVDYSKLVIEQLEKIEELYLHIIEQDEVNKKQQEHINNLELRMQKMEELLNNL
>NZ_CP047050.1|WP_158211266.1|3056487_3058164_-|gamma-glutamyltransferase
MRKILISAFVLCGSLLQVVAQNPETFKNGVIVSAHPEASKVGVDILKKGGNAVDAAVAVELALAVVYPNAGNIGGGGFIVYRGNDGTIDALDYREKAPMHARENMYWSGDGEAITDLSQNGTLATGIPGTVDGMVKAHQKYGTLSWAELVQPAIDLAEKGFAITAKQAKELTDHYAIFEKYNTQKNALTAKEHWKAGDLLVQSDLAETLKRVQKDGRKGFYEGKTAELIVAEMNRGNGMITLEDLKRYEAVWRTPIVGEYKGLKVISMPPPSSGGIALIALFQSIDQFPMKQWGFQSEKAVQVMTEASRRVYADRAEHLGDPAFHKVPTEKLVDKAYNVERLKTMSFDKATKSSDVSAGELSGYESDETTHYCVVDKWGNAVSATTTLNDSYGSKVVVGGAGFLLNNEMDDFSIKPGVPNMYGLVGGKANAIEPEKRMLSSMSPTILEKDDKLYMVVGTPGGSTIITSVFQTILNVVDFGMNMQEAVAAPRFHHQWLPDQIDYEPKALSTGVRKALQSKGYMLKERKPYGRVEGILVNADGTYQAGADPRGDDVAKGY
>NZ_CP047050.1|WP_158211265.1|3054931_3055948_-|hypothetical-protein
MNTTPITTVIDFSPFLGSNNLYGYRDQNNVVLIEPQYLEADKFVATGFAVVKSKNGLYGIISHTNKVVAPFHYSRILLTVVNHFTIAQVVITYQVRTEFWNWKLVPNLKLGIVKEKCKAFVIENRQLITTKVYTVDPDIKREPFLPIETIGERFVCIDQDLYKAKRARLKRIVKNYVGMFDNESKIVRKVNNEKVRVCNSRGRKVQSFETIHNEVFPITYKGKEHLVYLNKKDSMLKKAPVIYRDTKRSGRYYVNHEFDMPIPVHLKVIDLKRERPLVDIWKNVISVCPVPHKHFFIIEVRPMEEGQIENDFYFMNRLGTLQDYLEDETDFILANYLK
>NZ_CP047050.1|WP_158211264.1|3053754_3054873_+|FUSC-family-protein
MKDNFFVNLFVQESKTLFKLKHSERLWHIPLMAMLATGIPLLTGWYFNNLQAGLLACLAGLVILYLPSNIPTPQRMLTMLVCSFGFMLSFAVGITFSFNFVISSIAFGIFVTAVQWVNLYFNTRPPGSYFFIMVASMSSNMPFNLASIPTRLGYVVMGTMFACTLAMIYSLIVGKKYNSKTTAPLIVPVPIKKQVDYLIHSLIVGAFMFISLLTGHLLKLNNPYWIPASCAAIMQGISLYHVWQRALQRITGTFIGLGLCWLLISISDSPLYICICIMVLQFIIEMFVTRNYAVAVIFITALTVLLADAANPLISTPNALITARFLDIVIGSIIGGIGGWFIHHEYLRKQTRDGIRNTRLQLLKKMRRQERI
>NZ_CP047050.1|WP_158211263.1|3053067_3053415_-|hypothetical-protein
MQENEYIINGLKKEDSKRVKEHFTKHISFYRLKNCYRGVDGYFATGYSQLYLSYLRAGKAVEYRVIPFRYIISYAVTSIDSQTVKLKVWLVSGDVVECVFSENNIKDIVKILPSM
>NZ_CP047050.1|WP_158211262.1|3052879_3053056_-|hypothetical-protein
MTNPFIRIKASDGRQYLINIHHIVYVERVEEQKYAIHLVNDTVFTNTNVEELLDSLLS
>NZ_CP047050.1|WP_158211261.1|3052292_3052820_+|NADPH-dependent-FMN-reductase
MKIVAFAASNSSKSINLELIKAVSKQFGEHEVEILNLNDFEMPIYSQDRNEAGIPQLALDFNKHIQESDALIISLAEHNGSFSTAFKNIFDWGSRAEMKFFQEKPMLLLSTSPGARGGQTVMESAKGVFPYFGANIKNTFSFPSFYDNFKDGEIVNETLKQQVDEVIANFKSNLS
>NZ_CP047050.1|WP_158211260.1|3048076_3051898_-|hypothetical-protein
MRRKILLILFFVCNFAIYAQVGIGTKEPHISSILELNSSNKGLLIPQIELKSLSDRDVIEGRSPKIGLLVFNTTSIGNVLTPGYYYWGEYGNDRKEGWIRLGDDTIDFDVNRNESLSVDKEGILHLQDSNGSIVSIPLIELQLPSTLLPHKTKKGVFVYENEVNQKYEIHLIQEIINHIEDIFHSETVINYLVDQLKDKFGNVIYENNKFYYLNDNGDKVEIDWKDFNTKNVSFKLIKDELVITDSDGETVKLAVEEIAKSDKFVTELVNNQFFITELTENSFFIEKITTKKEFITKIINQLKGEYGNVFYENNKFYYLNENGDKVEINLGEFVKDNQKYTSVTAVSKTATTGKGLSIDTKEAGKDVVTFTETVTTANRFVKRAIANVTDADAKFTYYKYIDELGTERFITVSQDVSNDFETIINDNKTILEEFITNTTGDVKVIEKEGDIIFVVKEGDSVKEINITEIIKENTFVASLTNETVNESGVKAGFTFNNGKDTENVKFAETLTGLSQGRDAKNYIEYSYTDETGKAASTKITVTQDVINTFPEIIKDSEVIREIEKIITDKRSDISIVKEGDNYKITYVTENGTETIDLGEFVKDNQKYTSVTAVSKTATTGKGLTIDTKEAGKDVITFTETVTTANRFVKGAIANVTDVDAKFTYYKYIDELGTERFITVSQDVSNDFETIINDNKTILEEFITNTTGDVKVIEKEGDIIFVVKEGDSVKEINITEIIKENTFVASLTNETVNESGVKAGFTFNNGKDTENVKFAETLTGLSQGRDAKNYIEYSYTDETGKAASTKITVTQDVINTFPEIIKDSEVIREIEKIITDKRSDISIVKEGDNYKITYVTENGTETIDLGEFVKDNQKYTSVTAVSKTATTGKGLSIDTKEAGKDVVTFTETVTTANRFVKGAIANVTDADAKFTYYKYIDELGTERFITVSQDVSNDFETIINDNKTILEEFITNTTGDVKVIEKEGDIIFVVKEGDSVKEINITEIIKENTFVASLTNETVNESGVKAGFTFNNGKDTENVKFAETLTGLSQGRDAKNYIEYSYTDETGKVASTKITVTQDVINTFPEIIKEEKVITEIEKVVTDKGKNPWLNQGTEVVATEDAAEIAHRGSVAIGGNTLLTNSKATNTKLSVDGDVLVSGKFFSANSVFADYVFEKYFTGSTDLNLTYEFKSLDYVKDFIEKYNHLPGVTKISDIERTEDGRYLIDFTELSIQQLEKIEELYLHTIEQQGALDKMQDEVNILKARLDVLESLLTK
>NZ_CP047050.1|WP_158211259.1|3045850_3047974_+|dipeptidyl-carboxypeptidase-II
MKVKNAVIGVVAGASLFSISCNKTKSDATETVDWNENNAFFAESTLPYFTADFDKIKNKDFKPALLEGMRRQMEEIDKICANTEEPTFANTLEALERSSDLFDRVSSVFFLLTGAHTNDELKAVNAELAPKFASHSDGIYLNDALFQRIKKLHDNQAALNLNEEQARLLDVYYENFEKAGANLSAEDKEKLKQLNQDIATLNNDFGDKLLAATKEGGVKFTKEELAGLSDEELESIKQADGSYLIPLNNTTQQPDLDKLTNKESRKKLFEQAWIRAEKGDTNDTRATIITLAKKRAEKAKLMGFANYAEWSLQGTMASTPANAIQILKDLSPYAVGSAKEEAKDIQALINKEADPFTLTAADWNYYAEKIREDKFALNQNELKPYFEMNAVLEDGVFFMAKQLYGLTFKERKDIPVWQEDVKVYEVFNEDGSQVGLFYTDYYQRDSKRGGAWMSNIVGQSKLLNRLPVIYNVGNFPKPAAGQPTLLSQDNVITMFHEFGHAIHGFFANQTYPTLSGTNVSRDFVEFPSQFHEHFAFEPSVLKNYAKHYKTGEVIPQALVDKMKNAATFNKGYSMTELLGASLLDMEWHTISVDAEITDAIAFEQAALKKYGLDLATVPPRYRSTYFNHIFAGGYAAGYYSYKWSEMLDFDAYAWLEQNGGMTRANGQVLRDKVFSRGNSEPLDKLYKDFRGKNPSIDALLHYSGFTK
>NZ_CP047050.1|WP_158211258.1|3043655_3045641_-|S8-family-serine-peptidase
MKRIHSILFLSFFTLSVSAQNATVRKELALSYDTEQGKLLISKFQSEDKRDREKISEFLKRSKREEKGVFSDGRVFQIKRISEDGFPLYYTTSNLESRRVNQVEAIKEDLGITLDGQNMIVGVWDGQVALDIHREFIVNGVSEVKLGDAISSLENMTEKELKANQKSRNHATHVVGTIKAKGVFNKAKGMVPNAMVVSFDWINDASEMVAMAKEGLLVSNHSYGLAAVDEDLIPLVPVNYFGVYNKEASKFDRVAYTYPYFQSVVSAGNDRLEFDLVNESKHGDDLLLGTANAKNVIVVAATGVNEVGTNEVADFSSFGPSCDFRIKPDIAANGVRVISSGYANPEPLTAEPSIIRYAKMSGTSMAAPVVSGILTLWQQWAIENRQFPYKAATMKGVMVHSADYLRQKSPNNQIGWGVINAKKGVDLMINSLGENAIIEERLLLNEGEFKQKFILTENTNSLIVTLVWTDVEQDSPHYDFRTNRQAKALVNDLDLRVYKDGVAYFPWLLNKNYNDLRAVKGDNDVDNVEKIEIDNAEAGVYEIVVSHKGELQTGRQDFSLLVSNDEMKGISGEVVESLVSENDFIIWPNPIKDVFSIEIAKGKIFKFSQVDIYDLSNKLVKSVNVRATNRAVIDISELATGIYLMKIDAAGEKVRFKLAKK
>NZ_CP047050.1|WP_158211267.1|3061825_3062719_-|hypothetical-protein
MMKNIVRVGLLISCFSAWSQVGIGTHKPHKSAVLEVSSDTKGILLPKHVFEVFDDNQNPIVDPQVGTLVYNVMGGNHEDNIARKGIYVWDGKKWNQLLNNEGVDRMTTIRMMGGTAEATQEVLIPYTNLSATNYIRFKKEKTDYSTTDIERGVTLHYEYDNYGEVFTMPKGYYKVEVSIDGWNDRGNMSEDSNPDFHNPFIKDPNGNRHGYLGLYSKKCGITDVNGSELVPPQSATIISKHTRGGSIQGYTYMFFIRITDLEKKVKFRFTVSNDSSFKEGFRVNQNGVSIKFRRYFD
>NZ_CP047050.1|WP_158211268.1|3062715_3063615_-|hypothetical-protein
MKTNILKYSIASVLMLISINTLIAQTATNHHGVVSPAVILDMSTIDESIVQGDKAKGFVLPVVEIEDVLNKEEPIKNPAEGMLVYNNSKVIIPGVYMFKNGMWSAIVNRGSSIENAVIKVQNSTWQRPEEEPRYEIEIPLKEFDFDNTYGDVLLYDRADGLKDLMLRPGNYLIAFYLRGKIEDEGNMLNIENTLGDTNQSYRAHLINFRSEVRVDTAVVLNNAFADALVPFAVKENGSFRPLSREFSASFYFGLTIPEKEGGNQISNVKLILQAVEGTTFKKGNIIILDTYVNIEKSIL
>NZ_CP047050.1|WP_158211269.1|3063620_3064508_-|hypothetical-protein
MIYKAKVMRIGRFFLVTCLALIATTGYSQIGVNKRGVSANATAEFDVKDKGVLLPRVDIKNRYENNPIVGEQKDMPDGLVVIDVHDKEESTLSFWNNKLNGEKGAWEQLANFDRLPKTAIIGFELVDKTASSFEIPVTENGQMYLLNQNDFLFKILNDGHISSLSVLDAGKSNEIQLGFSSGVYLIEFFAVFIAPKEANRTYYNMAYFTNFNENYVTSLNQRIAATYRVERSTFSPEGEEHLVVFSNIMDLKKDKGKEVLHNFSLGVGKASNSTYYTAKYRLVAKNSYLKITKLK
>NZ_CP047050.1|WP_158211270.1|3064903_3066874_-|OmpA-family-protein
MKKNVIRFFSIASVFLVTMGGFAQGVKEKKADKSFDHYEYVNAIEIYEKIVDKGYKSINTLSKLAEAYYFKGDLKTAHKWYEELFTLAKQEDAKLPSESYYRYAQTLRGVENYEKADEYLGLFAKLEKSDSRGILFEEKKDTYLDEINAMIQRYDLESLPINSEYSDYGAAILGDKLVFTSARETEHGGKIHKWTNEAVTSLYMSTIASDGSFSEPELFDKSAKTKVNEASAIFTKDGKTMYFTRNNFKKNKKVYNSDYAILLKLYKATLNESGQWNEAVELPFNSDDFNTAHPALSPDEKWLYFASDRTGTIGESDIYRVAIYEDASFGTPENVGNRINTEGRETFPFISKDNYLYFSSDGRPGLGGLDVYMAKINVDGTFGKVVSVGAPINSSSDDFAFFINDKNRKGFVSSNREGGVGNDDIYFFQVVDCIQKIEGVVFDNSTKLPIVNATVVLFDANYKELGVITTDEEGHFATEAVECNRKFRLKASADDFLTAEVSTLLGKEFNVSKEVNIGLDPVEEKIGMDDDLFAKLKLDPIYFDFDKHSIRPDAAVELAKVVEVLKLYPQITIDVRAHTDSRGNDAYNMKLSERRAQSTRAWMISQGIEETRISAKGYGETQLVNQCANNVPCTKEEHQANRRSEFIIVKMDQSSF
>NZ_CP047050.1|WP_158211271.1|3066890_3067823_-|type-IX-secretion-system-membrane-protein-PorP/SprF
MNYNSILKKVGLCLVCLATAQQTFGQQDPQYTQYMYNPSNVNPAYAGSTGALSLFGHYRAQWVGLDGAPKTAHLSAHSPIGDSKLGIGGTFTNDKLGVMTENNISLDMSYTIDVNRDFKLAFGVKATANLLDVEYDKLHAYDPSAAELANNIKNKFNPNVGAGLYLYSDKAYVGLSVPNFLTTDRYDDNEITVMSQKAHFYVMGGYVFELNPSLKFKPAFLAKAVSGAPLQVDLTANFLFIDKFTVGAAYRWDASVSGLVGFQVNPNLMIGYSYDADTTKLANYNSGSHEFFLKFDIFNHKTKLNTPRFF
>NZ_CP047050.1|WP_158211386.1|3067834_3069088_-|gliding-motility-associated-C-terminal-domain-containing-protein
MKINYNTLLVVLSLTPLGTMAQTVNKGQLYVKAGSLLSTHYDFENKAKADFKNNGTFMVHKHLTNEGSFDYKGITPEGKTILMGKTTQVIVGDSLTKFNDLVLDNATEKMAFDIQNNMIVAGKADFLNGIGKVDKNKGAVTFLDKAEAANPSDKSHLEGAVEKEGKSDFTFPIGDQGMYRPAGTSMVKSNKDIFSAEYIYKDKPFFDERTKKAGVIQLVDNMEYWIIKKRDNKQENAIVTLSYDKRTTPAELLLEADKNLRIVRWNEKDKMWVDEGGIVDEANQTVTTPIAVEDVGYFTLATVKTDWMLDGEVVIYNFVSVNGTGHNEFFRIDNLNKYPDNRVEIYNRWGVKVYETTNYNSNGNVFKGYSEGRVTMNKNEKLPSGTYYFVVTYEYPDKSTGASRRIKKTGYLHLESN
>NZ_CP047050.1|WP_158211272.1|3069110_3069749_-|hypothetical-protein
MKKIYLGFAFTLLTTLGFAQTKIGVAGANNTPDVNANAVLELDATNKGLLLPRLALEKTTDATPLNEHVAGMTVYNTSKVNDVVPGFYYNDGTKWQQMVTTDNKAVKFFYMPSIVFDTSTVTADKLEEKDLYAEYTKQFGLKGNAVGSTGAPMADKGGIPHFPNATDLYYYVTDYDKTTFDEIVIDEKGLMKYKVIGTGSAYSIMNIVFVVK
>NZ_CP047050.1|WP_158211273.1|3069848_3072074_-|hypothetical-protein
MKKITLIAALLGSVYFANAQVGIGTPDPAVSAELEIFSTTKGLLIPRVELTDIKIYKPIEGSQVESLLVYNINEVNEVKDATDNNIITLPKGFYYWDGAKWNRIVSKSELDKAIENLGDNITKIGADVTNLKNLINYIVPTNPGNVDSDGKPVAGESHTTIVYDPKTGEMSYVTYDVTSKTYKTEKINLTNMIRGIETNTFFIELKDNNGKVTGYVYFNEAAITKAIEEALKIDPKATEADIIKGLNAKTPGAITIDVKEVVVNNIKEILESNPNITIQVDGKDKTFTTVEEYLQYITQFSEGNVIYTQIEDPNDANKKIWAFQYYDATTKAYKTINLNELVAAAETKTSIVTYNNKQYYLSESYINGGGEVDVTKWTAVPAGAIHIDVVGGVINNIEEILTTPGNITIQVDGKDKTFTTVEEYLQYITQFSEGNVIYKEIEVDKDPSDPNQGKEKVWVFQYYDAATNEYKTINLNDLVKGAETKTAITRTEAEVDGKLKDYAKVNAPVDVNVKKGEIFYKYDNEAGQPDYINMTGDILSSIENNEDIKNAITNVLNAGGNVYYGDHDGDDKNSAVTDKSPHVFYQVVYNDTTKKYENKEIDLPLSMLTKVINKYKDVVKKALGDNITNVGDIVLTGNVYNGRYVYLAKGTTKAGKEVAGTWVNSARTTGVDLPKATDDLAIKGILSIKLMKGDIVVANSATDIKLLGTKVEFNIGMGSQFIVVPTGDYDVVVEYTGDLVK
>NZ_CP047050.1|WP_158211274.1|3072109_3078508_-|DUF11-domain-containing-protein
MKNKTTFLLWKRLIIFLVLLVPLTYGYGQEKVYAKSAIFGTNNKITVLGIGSYKPTTDKNIANVIDVDKAVDKNLDSFASLFATNIAVVVGANGEAWIQTNFETAVPANTVAYVKVSAPINKGANLDLGKLVGGLLGVLGSNLIVEAYENDTTALNSKDVIVDFSETANGDLYLAISASKPFKGVRVSLRAEGSILNLLGGNKLEMNVYEAFYYKGDNSCGKPVSTAIEAKGLKIDLLGGLFELIGTKEFSKSIDNDVNSYSILKSGNFLNVGVGGHLSQYFNFPTTSAADATFNIKIGANESFLDLNVINALEVRAYNKNQLVYNRSLSGGLLNGTDLLTLLSGKESSILTFAPGKAFDKVELRINTAIGVGLANGGLCIYDVERYDGKTCVNPQVVVPAPTAVPFETASCATSIIDFENVDFATNAIDGNNETYASLIASAGSLLSSLPAHGMIQMGYDTTVPAYTTSYIRIDSQDEVLGKLLGGTLGKALDAVVGTLIGNSYFEVEAYNGSTSVAKTTSQNGFAGTTGGKMTVVQDKIGRYYLAVTPSSSYNSIKVTNKVSSIPNGETRTLKVYNMCREIGTDACFAPQFTSYDQKGVTLSLGKLGEAGAKNPYKAISDNSSEYSEISTGLITLGGSVGQMVYFNTPSQIGDELQVRLQLDPTSLASINLIGSYKVKTYLGDKEQETFGLQQGLVNNLDLLSLFKSGGIQTLKFDTRKTFDRVEINAFAGVNVSVTPAIRLYGVKRVNDACPVTTGVSPFISPVCATTLIGAENANDINNLFDGNFDSYTTLQSGAGILLGLGKMEGYVELGYENSVKANVTSYVRIDFESDKLKALLGGSLGNVVAGLLNNVLLGDHYFKVEVKDSKGRTVLEEGSQAVTSSFKNGKIRVIVDALGRTYLAITPSKEYKSIKITDVSKALVGATAAPNSMNVYGMCYETGSDTCAPAFATSYEYDGLGLSVNDLGKAGVTNPEWAINENTTNFSQISLGTLGVGASVKQFIYFNTLSVPNDVTKIRLKVGQGGVTVPLLESLEIIAYNGDAKVATLDWKNGLVEGVDVLSLINAGNVLDIPFKVAGRYDRISVGIKNVLNVGVFPPVELYGVTRSCSVYASSDVVSWKSYKVDGISKTTTVKGGEMVEYTIHVKNNGTASLLGFTVSDELPKGLTFISGGDFYNGKVHFTSDVELKVGSTTAFTFKAKVNDNLEGIDVIKNIAVVRVNQTGDEIPSFPPTDNNKPTTPDTTKKPGTEIGVTPNYDVAITKTGSSNGVNSNQALVGDELTYLITVKNTGNKDLKSFVIQDVISEAVPAVIEIIDNGGGIVDGNKITYKIGVLKVGESIDFTLKTKVNNAPSANEVVNKAVVTYKNTQGVEESKEVEYKLSTNCKPIDNKYIVIEGGGTGKNAVCYGTVVELKAKLYGLGKPKLDNPIFKWYKTKDRTDVPQIGSSITVTALVNTTYYVTVEDFGYCFQGDAAEVKVELLPMPAKPTVNGKSEVICSGDERILTVNEKAEFYQWYLNGVAIEGNVDKNATTEEQEKEAKRGKEKTFIADQPGVYTVRIKNKEACFSEPSDPIVIEYNPVPELEIEGGNRRGLKFDPGSNTSVSIKLPAVYTNGSNVVWHDHTGKKLKTGDIVEFTAPGIYTLTVSSESSNGCATFESLVVNVWDSSVCPPLTERVYATGVGNWKTTWFTTLGGFVAGKENATDTDPTTHSTISTTVALLGLGTTWQNIYFDGDQPVPAGTPVTIKLGKEYSGLVLAGGMSVVGLDANGKRIGAIKPVAGGVLDLLASDNVFEYTFVPSDKNGAQAYHGVQISLGALVGVAQLAKVYGVYYEKRVDAFSPGYCAPVTTGVHESVLDVLHGVQDIGLGVASATASVSHAWNAVDDDLETYAMISRGVAVANMASLTVVFKQQAVPGDKLHIITEVPGNPVLSLELIKGYKIQRYLGDQKVGEEIDGTGGVKVIDLKLLGIGYKNKFKMIIDEVDEPFDRVKISYGSIVGVLGNFTKVYEVSIAPKIDLGSNFDIEKDTKDICNSGVLEILPSDACSTYKIFTQEKGGDELTDLGNNKFKMPGKITPIEEVDDDGKPTGVLYEVIFVQTYRNGCLVGRRIPIKVKTKNCSVKSNLNVTHKIKI
>NZ_CP047050.1|WP_158211275.1|3080054_3081092_+|helix-turn-helix-transcriptional-regulator
MLPTLLSIELNPFVAVPMVAMNYFISGLFYGMVVLCLMSTLVIYKIFKERKWRLYFIIQILITCYFIIGDVQSYTTLKPELFDNYIQTGIIIAILMLTSLLLSTYFPFKTKKLFFKYELKIFTAISLIGIAFYFSNFLANPAMSPLLTVSIVIIFALTQYCIYKLSKTGKYLLYPILIILLIKFYTICFTQTKLFESIEEFTNSISALKVVAILIILFSIINNYVLIKKFQNRNIENQVVISQYVALLKNYHELLIEEKKAKAIKEAETVSLKDHQENLCEYLKANYKLTERELHVLYHIWDGMSNKEIASELNISLSTTKYHISNIYLKLNVNSRPQVFALKDW

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP047050_3	3.45\|2146977\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2146977-2147010	34	NZ_CP047050.1	1766791-1766824	0	1.0

1. spacer 3.45|2146977|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to position: 1766791-1766824, mismatch: 0, identity: 1.0

aagcaaaaatcaaagaaagaagaagataatcaac	CRISPR spacer
aagcaaaaatcaaagaaagaagaagataatcaac	Protospacer
**********************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	MT708547	Klebsiella phage Muenster, complete genome	305153-305186	7	0.794
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	AB897757	Klebsiella phage K64-1 DNA, complete genome	182257-182290	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MK268686	Enterococcus phage vB_EfaH_EF1TV, complete genome	58622-58655	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AP018715	Enterococcus phage phiM1EF22 DNA, complete sequence	21634-21667	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MK721192	Enterococcus phage vB_EfaM_Ef2.3, complete genome	61593-61626	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	CAJDJZ010000002	Enterococcus phage vB_EfaH_149 genome assembly, contig: phage149-genome, whole genome shotgun sequence	23454-23487	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NC_029026	Enterococcus phage EFLK1, complete genome	107729-107762	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AP018714	Enterococcus phage phiEF17H DNA, complete sequence	23434-23467	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MK693030	Enterococcus phage vB_EfaM_Ef2.1, complete genome	57338-57371	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NC_009904	Enterococcus phage phiEF24C, complete genome	20902-20935	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AP009390	Enterococcus phage phiEF24C DNA, complete genome	20902-20935	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	CAJDJY010000002	Enterococcus phage 156 genome assembly, contig: phage156-genome, whole genome shotgun sequence	23344-23377	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MN854830	Enterococcus phage PBEF129, complete genome	57541-57574	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	KJ801817	Enterococcus phage ECP3, complete genome	75065-75098	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AB609718	Enterococcus phage phiEF24C-P2 DNA, complete genome	20902-20935	7	0.794
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	LR031359	Enterococcus phage 156, complete genome	23344-23377	7	0.794
NZ_CP047050_3	3.5\|2144352\|36\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144352-2144387	36	NZ_CP045339	Vibrio sp. THAF190c plasmid pTHAF190c_a, complete sequence	1401962-1401997	8	0.778
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NZ_CP047444	Spiroplasma citri strain BLH-MB plasmid pSciBLHMB-7	30308-30341	8	0.765
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MN693807	Marine virus AFVG_250M375, complete genome	14465-14498	8	0.765
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NZ_LR215005	Mycoplasma conjunctivae strain NCTC10147 plasmid 9	128619-128652	8	0.765
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MG592576	Vibrio phage 1.206.O._10N.222.51.B10, partial genome	12624-12657	8	0.765
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AP014182	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C67-MedDCM-OCT-S41-C49, * SEQUENCING IN PROGRESS *	23672-23705	8	0.765
NZ_CP047050_3	3.45\|2146977\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2146977-2147010	34	MG945356	UNVERIFIED: Microviridae sp. isolate 2769-1801, complete genome	2421-2454	8	0.765
NZ_CP047050_3	3.45\|2146977\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2146977-2147010	34	NZ_CP023318	Bacillus megaterium strain A plasmid p1, complete sequence	20210-20243	8	0.765
NZ_CP047050_3	3.67\|2148424\|35\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2148424-2148458	35	MN692965	Marine virus AFVG_117M92, complete genome	32062-32096	8	0.771
NZ_CP047050_3	3.68\|2148489\|35\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2148489-2148523	35	MH319749	Marine virus AG-345-F15 Ga0172271_11 genomic sequence	83655-83689	8	0.771
NZ_CP047050_3	3.12\|2144811\|36\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144811-2144846	36	NZ_CP009639	Bacillus cereus 03BB108 plasmid pBFI_1, complete sequence	165783-165818	9	0.75
NZ_CP047050_3	3.12\|2144811\|36\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144811-2144846	36	NZ_CP053963	Bacillus cereus strain FDAARGOS_802 plasmid unnamed3, complete sequence	207368-207403	9	0.75
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019095	Synechococcus phage ACG-2014f isolate Syn7803US34, complete genome	182774-182807	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019086	Synechococcus phage ACG-2014f isolate Syn7803US17, complete genome	180055-180088	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019106	Synechococcus phage ACG-2014f isolate Syn7803US50, complete genome	176713-176746	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019107	Synechococcus phage ACG-2014f isolate Syn7803US52, complete genome	174561-174594	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019143	Synechococcus phage ACG-2014f isolate Syn7803C12, complete genome	177210-177243	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019102	Synechococcus phage ACG-2014f isolate Syn7803US43, complete genome	178669-178702	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019066	Synechococcus phage ACG-2014f isolate Syn7803C9, complete genome	179930-179963	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019142	Synechococcus phage ACG-2014f isolate Syn7803C11, complete genome	176475-176508	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019149	Synechococcus phage ACG-2014f isolate Syn7803C21, complete genome	176204-176237	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019105	Synechococcus phage ACG-2014f isolate Syn7803US4, complete genome	176000-176033	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019098	Synechococcus phage ACG-2014f isolate Syn7803US39, complete genome	180491-180524	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019159	Synechococcus phage ACG-2014f isolate Syn7803C34, complete genome	178840-178873	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019123	Synechococcus phage ACG-2014f isolate Syn7803US7, complete genome	173817-173850	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019111	Synechococcus phage ACG-2014f isolate Syn7803US57, complete genome	175825-175858	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019148	Synechococcus phage ACG-2014f isolate Syn7803C19, complete genome	173725-173758	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	NC_047712	Synechococcus phage ACG-2014f isolate Syn7803C7, complete genome	176690-176723	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019090	Synechococcus phage ACG-2014f isolate Syn7803US24, complete genome	178826-178859	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019146	Synechococcus phage ACG-2014f isolate Syn7803C16, complete genome	179217-179250	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019152	Synechococcus phage ACG-2014f isolate Syn7803C25, complete genome	179836-179869	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019093	Synechococcus phage ACG-2014f isolate Syn7803US30, complete genome	175401-175434	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019151	Synechococcus phage ACG-2014f isolate Syn7803C24, complete genome	178287-178320	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019150	Synechococcus phage ACG-2014f isolate Syn7803C22, complete genome	180344-180377	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	NC_026927	Synechococcus phage ACG-2014f isolate Syn7803C90, complete genome	181581-181614	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019097	Synechococcus phage ACG-2014f isolate Syn7803US37, complete genome	182187-182220	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019045	Synechococcus phage ACG-2014f isolate Syn7803C6, complete genome	179377-179410	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019037	Synechococcus phage ACG-2014f isolate Syn7803C58, complete genome	178956-178989	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019099	Synechococcus phage ACG-2014f isolate Syn7803US3, complete genome	179230-179263	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019155	Synechococcus phage ACG-2014f isolate Syn7803C29, complete genome	175859-175892	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019141	Synechococcus phage ACG-2014f isolate Syn7803C10, complete genome	175261-175294	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019053	Synechococcus phage ACG-2014f isolate Syn7803C80, complete genome	179282-179315	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019147	Synechococcus phage ACG-2014f isolate Syn7803C17, complete genome	175669-175702	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019100	Synechococcus phage ACG-2014f isolate Syn7803US40, complete genome	176858-176891	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019101	Synechococcus phage ACG-2014f isolate Syn7803US42, complete genome	176947-176980	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019085	Synechococcus phage ACG-2014f isolate Syn7803US13, complete genome	175619-175652	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019096	Synechococcus phage ACG-2014f isolate Syn7803US36, complete genome	179566-179599	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019091	Synechococcus phage ACG-2014f isolate Syn7803US26, complete genome	175791-175824	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019144	Synechococcus phage ACG-2014f isolate Syn7803C14, complete genome	175820-175853	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019145	Synechococcus phage ACG-2014f isolate Syn7803C15, complete genome	178951-178984	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019058	Synechococcus phage ACG-2014f isolate Syn7803C8, complete genome	176534-176567	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019092	Synechococcus phage ACG-2014f isolate Syn7803US2, complete genome	178277-178310	9	0.735
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	NZ_CP049914	Vibrio sp. HDW18 plasmid p_unnamed1, complete sequence	79486-79519	9	0.735
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MN693193	Marine virus AFVG_25M440, complete genome	24354-24387	9	0.735
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NZ_CP020413	Leptospira interrogans serovar Copenhageni strain FDAARGOS_203 plasmid unnamed1, complete sequence	229551-229584	9	0.735
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	MG065692	UNVERIFIED: Campylobacter phage C13, complete genome	5304-5337	9	0.735
NZ_CP047050_3	3.60\|2147960\|36\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2147960-2147995	36	CP015514	Vibrio vulnificus strain FORC_036 plasmid unnamed, complete sequence	875902-875937	9	0.75
NZ_CP047050_3	3.67\|2148424\|35\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2148424-2148458	35	NC_011061	Prosthecochloris aestuarii DSM 271 plasmid pPAES01, complete sequence	27293-27327	9	0.743
NZ_CP047050_3	3.14\|2144942\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2144942-2144975	34	KJ019103	Synechococcus phage ACG-2014f isolate Syn7803US44, complete genome	179094-179127	10	0.706
NZ_CP047050_3	3.67\|2148424\|35\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2148424-2148458	35	CP012553	Campylobacter sp. RM16192 plasmid p16192, complete sequence	15392-15426	10	0.714
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	NZ_LR214939	Mycoplasma salivarium strain NCTC10113 plasmid 2	224044-224077	11	0.676
NZ_CP047050_3	3.20\|2145338\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2145338-2145371	34	AP014180	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C67-MedDCM-OCT-S37-C48, * SEQUENCING IN PROGRESS *	19603-19636	11	0.676
NZ_CP047050_3	3.53\|2147500\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2147500-2147533	34	NC_006129	Borreliella bavariensis PBi plasmid lp54, complete sequence	13787-13820	11	0.676
NZ_CP047050_3	3.53\|2147500\|34\|NZ_CP047050\|PILER-CR,CRISPRCasFinder,CRT	2147500-2147533	34	MN855789	Bacteriophage sp. isolate 75, partial genome	1969-2002	11	0.676

1. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MT708547 (Klebsiella phage Muenster, complete genome) position: , mismatch: 7, identity: 0.794

gaaattgc--agaatctaaaagacgtgatgcagaat	CRISPR spacer
--gattgctgggaatctgaaggacgtgatgcagaac	Protospacer
  .*****  .******.**.**************.

2. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AB897757 (Klebsiella phage K64-1 DNA, complete genome) position: , mismatch: 7, identity: 0.794

gaaattgc--agaatctaaaagacgtgatgcagaat	CRISPR spacer
--gattgctgggaatctgaaggacgtgatgcagaac	Protospacer
  .*****  .******.**.**************.

3. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MK268686 (Enterococcus phage vB_EfaH_EF1TV, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

4. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AP018715 (Enterococcus phage phiM1EF22 DNA, complete sequence) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

5. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MK721192 (Enterococcus phage vB_EfaM_Ef2.3, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

6. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to CAJDJZ010000002 (Enterococcus phage vB_EfaH_149 genome assembly, contig: phage149-genome, whole genome shotgun sequence) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

7. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_029026 (Enterococcus phage EFLK1, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

8. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AP018714 (Enterococcus phage phiEF17H DNA, complete sequence) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

9. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MK693030 (Enterococcus phage vB_EfaM_Ef2.1, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

10. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_009904 (Enterococcus phage phiEF24C, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

11. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AP009390 (Enterococcus phage phiEF24C DNA, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

12. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to CAJDJY010000002 (Enterococcus phage 156 genome assembly, contig: phage156-genome, whole genome shotgun sequence) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

13. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MN854830 (Enterococcus phage PBEF129, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

14. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ801817 (Enterococcus phage ECP3, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

15. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AB609718 (Enterococcus phage phiEF24C-P2 DNA, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

16. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to LR031359 (Enterococcus phage 156, complete genome) position: , mismatch: 7, identity: 0.794

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aacaatgttaaaaaagcaatggaagaggctagac	Protospacer
.*.*.**.******************.****.*

17. spacer 3.5|2144352|36|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP045339 (Vibrio sp. THAF190c plasmid pTHAF190c_a, complete sequence) position: , mismatch: 8, identity: 0.778

-aatcgtatagaatatgtattcattttttttttttta	CRISPR spacer
ttagcg-aagaaatatgtattcatttttgtgttttta	Protospacer
  * ** * ..***************** * ******

18. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP047444 (Spiroplasma citri strain BLH-MB plasmid pSciBLHMB-7) position: , mismatch: 8, identity: 0.765

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aaagatattaaaaaagcaatggaagaagttataa	Protospacer
.* ..*..********************.** **

19. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MN693807 (Marine virus AFVG_250M375, complete genome) position: , mismatch: 8, identity: 0.765

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
agtataactaaaaaagcaatgaaagaagctgaag	Protospacer
..**  .**************.********.**.

20. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR215005 (Mycoplasma conjunctivae strain NCTC10147 plasmid 9) position: , mismatch: 8, identity: 0.765

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aaaacaacaaaaaaagctatgcaagaagctaaaa	Protospacer
.* *  .* ******** *** ************

21. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MG592576 (Vibrio phage 1.206.O._10N.222.51.B10, partial genome) position: , mismatch: 8, identity: 0.765

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
gctgatgctaaaaaagcaatagatgaagctgagc	Protospacer
* *..***************.** ******.*.

22. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AP014182 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C67-MedDCM-OCT-S41-C49, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 8, identity: 0.765

gatag-tgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
-acagttcctacaaaagcaatggaagaaggtactg	Protospacer
 *.** * *** ***************** **  .

23. spacer 3.45|2146977|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MG945356 (UNVERIFIED: Microviridae sp. isolate 2769-1801, complete genome) position: , mismatch: 8, identity: 0.765

aagcaaaaatcaaagaaagaagaagataatcaac	CRISPR spacer
gagccaaaatcaaagaaagaagaagcagacaaat	Protospacer
.*** ********************  .*. **.

24. spacer 3.45|2146977|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023318 (Bacillus megaterium strain A plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.765

aagcaaaaatcaaagaaagaagaagataatcaac	CRISPR spacer
aattaaaaagcaaagaaagaagacgataagaata	Protospacer
** .***** ************* *****  *

25. spacer 3.67|2148424|35|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MN692965 (Marine virus AFVG_117M92, complete genome) position: , mismatch: 8, identity: 0.771

cctttaataacaataaaaaactgtaaaaaagtatt	CRISPR spacer
catcaaataacaataaaaaactttaaaaaatgaca	Protospacer
* *. ***************** *******  *.

26. spacer 3.68|2148489|35|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MH319749 (Marine virus AG-345-F15 Ga0172271_11 genomic sequence) position: , mismatch: 8, identity: 0.771

aaaaaatatctaaatgatccgtattttttaaagaa	CRISPR spacer
cgaagatatctacatgatccgtattttccaagtaa	Protospacer
 .**.******* **************..**. **

27. spacer 3.12|2144811|36|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009639 (Bacillus cereus 03BB108 plasmid pBFI_1, complete sequence) position: , mismatch: 9, identity: 0.75

aggagtacaacttgaattattttaaatataaatctt	CRISPR spacer
aggtgtacaactagaattattttaaaaagggaggat	Protospacer
*** ******** ************* * ..*   *

28. spacer 3.12|2144811|36|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053963 (Bacillus cereus strain FDAARGOS_802 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.75

aggagtacaacttgaattattttaaatataaatctt	CRISPR spacer
aggtgtacaactagaattattttaaaaagggaggat	Protospacer
*** ******** ************* * ..*   *

29. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019095 (Synechococcus phage ACG-2014f isolate Syn7803US34, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

30. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019086 (Synechococcus phage ACG-2014f isolate Syn7803US17, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

31. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019106 (Synechococcus phage ACG-2014f isolate Syn7803US50, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

32. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019107 (Synechococcus phage ACG-2014f isolate Syn7803US52, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

33. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019143 (Synechococcus phage ACG-2014f isolate Syn7803C12, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

34. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019102 (Synechococcus phage ACG-2014f isolate Syn7803US43, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

35. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019066 (Synechococcus phage ACG-2014f isolate Syn7803C9, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

36. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019142 (Synechococcus phage ACG-2014f isolate Syn7803C11, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

37. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019149 (Synechococcus phage ACG-2014f isolate Syn7803C21, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

38. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019105 (Synechococcus phage ACG-2014f isolate Syn7803US4, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

39. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019098 (Synechococcus phage ACG-2014f isolate Syn7803US39, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

40. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019159 (Synechococcus phage ACG-2014f isolate Syn7803C34, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

41. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019123 (Synechococcus phage ACG-2014f isolate Syn7803US7, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

42. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019111 (Synechococcus phage ACG-2014f isolate Syn7803US57, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

43. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019148 (Synechococcus phage ACG-2014f isolate Syn7803C19, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

44. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_047712 (Synechococcus phage ACG-2014f isolate Syn7803C7, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

45. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019090 (Synechococcus phage ACG-2014f isolate Syn7803US24, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

46. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019146 (Synechococcus phage ACG-2014f isolate Syn7803C16, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

47. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019152 (Synechococcus phage ACG-2014f isolate Syn7803C25, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

48. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019093 (Synechococcus phage ACG-2014f isolate Syn7803US30, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

49. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019151 (Synechococcus phage ACG-2014f isolate Syn7803C24, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

50. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019150 (Synechococcus phage ACG-2014f isolate Syn7803C22, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

51. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_026927 (Synechococcus phage ACG-2014f isolate Syn7803C90, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

52. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019097 (Synechococcus phage ACG-2014f isolate Syn7803US37, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

53. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019045 (Synechococcus phage ACG-2014f isolate Syn7803C6, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

54. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019037 (Synechococcus phage ACG-2014f isolate Syn7803C58, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

55. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019099 (Synechococcus phage ACG-2014f isolate Syn7803US3, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

56. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019155 (Synechococcus phage ACG-2014f isolate Syn7803C29, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

57. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019141 (Synechococcus phage ACG-2014f isolate Syn7803C10, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

58. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019053 (Synechococcus phage ACG-2014f isolate Syn7803C80, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

59. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019147 (Synechococcus phage ACG-2014f isolate Syn7803C17, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

60. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019100 (Synechococcus phage ACG-2014f isolate Syn7803US40, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

61. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019101 (Synechococcus phage ACG-2014f isolate Syn7803US42, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

62. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019085 (Synechococcus phage ACG-2014f isolate Syn7803US13, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

63. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019096 (Synechococcus phage ACG-2014f isolate Syn7803US36, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

64. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019091 (Synechococcus phage ACG-2014f isolate Syn7803US26, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

65. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019144 (Synechococcus phage ACG-2014f isolate Syn7803C14, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

66. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019145 (Synechococcus phage ACG-2014f isolate Syn7803C15, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

67. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019058 (Synechococcus phage ACG-2014f isolate Syn7803C8, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

68. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019092 (Synechococcus phage ACG-2014f isolate Syn7803US2, complete genome) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcctgctgaatctaaaatacgtgatgcactat	Protospacer
    .*** ********** **********  **

69. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049914 (Vibrio sp. HDW18 plasmid p_unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
ggcagagcaaaatctagaagacgtgatgcaagag	Protospacer
*. *  ***.******.*************..*

70. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MN693193 (Marine virus AFVG_25M440, complete genome) position: , mismatch: 9, identity: 0.735

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aagaaaaagaaagaagcaatagaagaagctaaaa	Protospacer
.* *. .  ***.*******.*************

71. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP020413 (Leptospira interrogans serovar Copenhageni strain FDAARGOS_203 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
ggaatcattcaaaaagcaatggaaaaagcaaaaa	Protospacer
*. * ...* **************.**** ****

72. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MG065692 (UNVERIFIED: Campylobacter phage C13, complete genome) position: , mismatch: 9, identity: 0.735

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aatgacactaaaaaagaaatgaaagaagctacca	Protospacer
.**....********* ****.*********  *

73. spacer 3.60|2147960|36|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to CP015514 (Vibrio vulnificus strain FORC_036 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.75

aaattaatttcaactccttttgttttttctacaaat	CRISPR spacer
ctattaatttcaacttcttttatttttttatctaag	Protospacer
  *************.*****.******.  * **

74. spacer 3.67|2148424|35|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_011061 (Prosthecochloris aestuarii DSM 271 plasmid pPAES01, complete sequence) position: , mismatch: 9, identity: 0.743

cctttaataacaataaaaaactgtaaaaaagtatt	CRISPR spacer
aattcaataacaataaaaaactttaaaaagtaaag	Protospacer
  **.***************** ******.  *

75. spacer 3.14|2144942|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to KJ019103 (Synechococcus phage ACG-2014f isolate Syn7803US44, complete genome) position: , mismatch: 10, identity: 0.706

gaaattgcagaatctaaaagacgtgatgcagaat	CRISPR spacer
tttcccgctgaatctaaaatacgtgatgcactat	Protospacer
    ..** ********** **********  **

76. spacer 3.67|2148424|35|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to CP012553 (Campylobacter sp. RM16192 plasmid p16192, complete sequence) position: , mismatch: 10, identity: 0.714

cctttaataacaataaaaaactgtaaaaaagtatt	CRISPR spacer
gatgaagaaacaataaaaaaatgtaaaaaactacg	Protospacer
  *  *. ************ ********* **.

77. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR214939 (Mycoplasma salivarium strain NCTC10113 plasmid 2) position: , mismatch: 11, identity: 0.676

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
aaacaagctaaaaaagctattgaagaagctgctg	Protospacer
.*  . *********** ** *********.  .

78. spacer 3.20|2145338|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to AP014180 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C67-MedDCM-OCT-S37-C48, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 11, identity: 0.676

gatagtgctaaaaaagcaatggaagaagctaaaa	CRISPR spacer
actgtacctacaaaagcaatggaagaaggtactg	Protospacer
. *.   *** ***************** **  .

79. spacer 3.53|2147500|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to NC_006129 (Borreliella bavariensis PBi plasmid lp54, complete sequence) position: , mismatch: 11, identity: 0.676

ggaattggagtacttgcaattgttgctacttgtg	CRISPR spacer
cctccttttatacttgcaattgttactacttttg	Protospacer
    .*   .**************.****** **

80. spacer 3.53|2147500|34|NZ_CP047050|PILER-CR,CRISPRCasFinder,CRT matches to MN855789 (Bacteriophage sp. isolate 75, partial genome) position: , mismatch: 11, identity: 0.676

ggaattggagtacttgcaattgttgctacttgtg	CRISPR spacer
ttgggtggtgtatttgcaattgttgctacagtgg	Protospacer
  .. *** ***.****************    *

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1090405 : 1106032

Pandoravirus(11.11%)

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_158209865.1\|1090405_1091056_+	HD domain-containing protein	S4W232	Pandoravirus	1.1e-13	28.2
WP_158209866.1\|1091318_1092719_+	DASS family sodium-coupled anion symporter	Q6A201	Oenococcus_phage	2.8e-14	23.9
WP_158209867.1\|1092792_1094691_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	4.6e-12	24.0
WP_158209868.1\|1094761_1095691_-	sugar kinase	NA	NA	NA	NA
WP_090409923.1\|1096327_1096798_-	ribonuclease HI	A0A223LIW7	Erwinia_phage	3.9e-21	39.6
WP_158209869.1\|1096790_1097366_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	2.9e-18	29.3
WP_002988156.1\|1097563_1097800_+	acyl carrier protein	B2ZXV3	Ralstonia_phage	1.8e-06	38.1
WP_158209870.1\|1097995_1099249_+	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_158211329.1\|1099264_1100011_+	ribonuclease III	A0A2K9R4Y7	Dishui_lake_phycodnavirus	1.9e-17	35.2
WP_158209871.1\|1100111_1100603_+	IPExxxVDY family protein	NA	NA	NA	NA
WP_158209872.1\|1100607_1102038_+	pyruvate kinase	NA	NA	NA	NA
WP_158209873.1\|1102163_1102769_-	superoxide dismutase	Q56AR7	Bacillus_thuringiensis_phage	2.4e-63	58.9
WP_158209874.1\|1102879_1106032_+	UvrD-helicase domain-containing protein	A0A1P8CWU5	Bacillus_phage	3.9e-08	22.0

DBSCAN-SWA_2

2971625 : 2978123

Enterobacteria_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_158211213.1\|2971625_2972504_-	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	7.9e-100	62.2
WP_158211214.1\|2972605_2973652_-	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	3.5e-86	50.3
WP_158211215.1\|2973655_2974867_-	UDP-N-acetyl-D-mannosamine dehydrogenase	A0A127AXI2	Bacillus_phage	1.4e-25	26.0
WP_158211216.1\|2974925_2976044_-	UDP-N-acetylglucosamine 2-epimerase (non-hydrolyzing)	A0A1V0SAG5	Catovirus	6.4e-30	29.9
WP_158211217.1\|2976064_2977462_-	nucleotide sugar dehydrogenase	A0A127AXI2	Bacillus_phage	2.3e-69	35.5
WP_158211218.1\|2977688_2978123_-	adenylyltransferase/cytidyltransferase family protein	A0A218MN49	uncultured_virus	1.5e-38	55.0

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_CP047050

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection