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_CP017169	Myxococcus xanthus strain GH3.5.6c2 chromosome, complete genome	14 crisprs	cas3,WYL,Cas9_archaeal,csa3,2OG_CAS,RT,DinG,cas2,cas1,cas4,cas7,cas8c,cas5,DEDDh	2	57	10	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP017169_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_1

217636-217943

Orphan

Consensus_repeat	Method
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP017169_1

>merge|NZ_CP017169|1|217636-217943|CRISPRCasFinder
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGCCAGGATCTGCTCCTGCGTGAGGTCCTTGAAGCCCAGCTCGCGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGCGATGACGTCATCCGAATCCGTGCTCTGGAATCCCAGTTCGCGCATCTGCTTCACGAAGTCGGGCGTGACGCCGTGGATGCCCATGGCCATCAGCTGATTCCAGGGCAGCTTCGTGAAGCCGGCGCCGGCGAGCTCCTTCACGCGCTGGGGCGTGACGCCGTGGATGCGGCCCTC

>NZ_CP017169|1|1|217636-217943|CRISPRCasFinder
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	CAGGATCTGCTCCTGCGTGAGGTCCTTGAAGCCCAGCTCG
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	GATGACGTCATCCGAATCCGTGCTCTGGAATCCCAGTTCG
CGCATCTGCTTCACGAAGTCGGGCGTGACGCCGTGGATGCCCATGGC	CATCAGCTGATTCCAGGGCAGCTTCGTGAAGCCGGCGCCG
GCGAGCTCCTTCACGCGCTGGGGCGTGACGCCGTGGATGCGGCCCTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140796922.1\|215030_216962_+\|DUF885-family-protein	unknown	unknown	gnl\|CDD\|377577
NZ_CP017169.1\|WP_140852806.1\|209068_211771_-\|AsmA-family-protein	unknown	unknown	gnl\|CDD\|282957
NZ_CP017169.1\|WP_174258590.1\|230214_232731_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_140796920.1\|212135_212555_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140852803.1\|203876_204758_-\|TSUP-family-transporter	unknown	unknown	gnl\|CDD\|376667
NZ_CP017169.1\|WP_140796925.1\|222724_223828_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140786652.1\|221277_222093_-\|sterol-desaturase-family-protein	unknown	unknown	gnl\|CDD\|377224
NZ_CP017169.1\|WP_174258588.1\|225393_228252_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP017169.1\|WP_140786644.1\|206330_207617_-\|sigma-54-interacting-transcriptional-regulator	unknown	unknown	gnl\|CDD\|226350
NZ_CP017169.1\|WP_026113917.1\|220732_221128_-\|BlaI/MecI/CopY-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367747
NZ_CP017169.1\|WP_140796924.1\|222371_222716_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140852804.1\|204754_205366_-\|rhodanese-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|238089
NZ_CP017169.1\|WP_140852811.1\|232801_233317_-\|GreA/GreB-family-elongation-factor	unknown	unknown	gnl\|CDD\|334464
NZ_CP017169.1\|WP_140852807.1\|212567_213269_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_174259028.1\|207646_208861_-\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223523
NZ_CP017169.1\|WP_140852805.1\|205383_206088_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293810
NZ_CP017169.1\|WP_174258589.1\|228485_230210_+\|GAF-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_140800574.1\|216970_217381_-\|fibril-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140852808.1\|218612_220736_-\|M56-family-metallopeptidase	unknown	unknown	gnl\|CDD\|320700
NZ_CP017169.1\|WP_140786655.1\|223843_225280_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238742

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140796922.1\|215030_216962_+\|DUF885-family-protein	gnl\|CDD\|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	3.42047e-71
NZ_CP017169.1\|WP_140852806.1\|209068_211771_-\|AsmA-family-protein	gnl\|CDD\|282957	pfam05170, AsmA, AsmA family. The AsmA gene, whose product is involved in the assembly of outer membrane proteins in Escherichia coli. AsmA mutations were isolated as extragenic suppressors of an OmpF assembly mutant. AsmA may have a role in LPS biogenesis.	3.12653e-10
NZ_CP017169.1\|WP_174258590.1\|230214_232731_-\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.19285e-55
NZ_CP017169.1\|WP_140852803.1\|203876_204758_-\|TSUP-family-transporter	gnl\|CDD\|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	6.05278e-33
NZ_CP017169.1\|WP_140786652.1\|221277_222093_-\|sterol-desaturase-family-protein	gnl\|CDD\|377224	pfam04116, FA_hydroxylase, Fatty acid hydroxylase superfamily. This superfamily includes fatty acid and carotene hydroxylases and sterol desaturases. Beta-carotene hydroxylase is involved in zeaxanthin synthesis by hydroxylating beta-carotene, but the enzyme may be involved in other pathways. This family includes C-5 sterol desaturase and C-4 sterol methyl oxidase. Members of this family are involved in cholesterol biosynthesis and biosynthesis a plant cuticular wax. These enzymes contain two copies of a HXHH motif. Members of this family are integral membrane proteins.	1.02458e-20
NZ_CP017169.1\|WP_174258588.1\|225393_228252_-\|PAS-domain-S-box-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	1.68556e-61
NZ_CP017169.1\|WP_140786644.1\|206330_207617_-\|sigma-54-interacting-transcriptional-regulator	gnl\|CDD\|226350	COG3829, RocR, Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains [Transcription / Signal transduction mechanisms].	3.86831e-133
NZ_CP017169.1\|WP_026113917.1\|220732_221128_-\|BlaI/MecI/CopY-family-transcriptional-regulator	gnl\|CDD\|367747	pfam03965, Penicillinase_R, Penicillinase repressor. The penicillinase repressor negatively regulates expression of the penicillinase gene. The N-terminal region of this protein is involved in operator recognition, while the C-terminal is responsible for dimerization of the protein.	8.74465e-26
NZ_CP017169.1\|WP_140852804.1\|204754_205366_-\|rhodanese-like-domain-containing-protein	gnl\|CDD\|238089	cd00158, RHOD, Rhodanese Homology Domain (RHOD); an alpha beta fold domain found duplicated in the rhodanese protein. The cysteine containing enzymatically active version of the domain is also found in the Cdc25 class of protein phosphatases and a variety of proteins such as sulfide dehydrogenases and certain stress proteins such as senesence specific protein 1 in plants, PspE and GlpE in bacteria and cyanide and arsenate resistance proteins. Inactive versions (no active site cysteine) are also seen in dual specificity phosphatases, ubiquitin hydrolases from yeast and in sulfuryltransferases, where they are believed to play a regulatory role in multidomain proteins.	2.26771e-22
NZ_CP017169.1\|WP_140852811.1\|232801_233317_-\|GreA/GreB-family-elongation-factor	gnl\|CDD\|334464	pfam01272, GreA_GreB, Transcription elongation factor, GreA/GreB, C-term. This domain has an FKBP-like fold.	5.71704e-13
NZ_CP017169.1\|WP_174259028.1\|207646_208861_-\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|223523	COG0446, HcaD, Uncharacterized NAD(FAD)-dependent dehydrogenases [General function prediction only].	3.73857e-35
NZ_CP017169.1\|WP_140852805.1\|205383_206088_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293810	cd07724, POD-like_MBL-fold, ETHE1 (PDO type I), persulfide dioxygenase A (PDOA, PDO type II) and related proteins; MBL-fold metallo-hydrolase domain. Persulfide dioxygenase (PDO, also known as sulfur dioxygenase, SDO, EC 1.13.11.18) is a non-heme iron-dependent oxygenase which catalyzes the oxidation of glutathione persulfide to glutathione and persulfite in the mitochondria. Mutations in ethe1 (the human PDO gene) are responsible for a rare autosomal recessive metabolic disorder called ethylmalonic encephalopathy. Arabidopsis thaliana ETHE1 is essential for embryo and endosperm development. Bacterial ETHE1-type PDOs are also called Type 1 PDOs. Type II PDOs (also called PDOAs), are mainly proteobacterial. These enzymes belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions.	7.47124e-82
NZ_CP017169.1\|WP_174258589.1\|228485_230210_+\|GAF-domain-containing-sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.32055e-53
NZ_CP017169.1\|WP_140852808.1\|218612_220736_-\|M56-family-metallopeptidase	gnl\|CDD\|320700	cd07341, M56_BlaR1_MecR1_like, Peptidase M56-like including those in BlaR1 and MecR1, integral membrane metallopeptidase. This family contains peptidase M56, which includes zinc metalloprotease domain in MecR1 as well as BlaR1. MecR1 is a transmembrane beta-lactam sensor/signal transducer protein that regulates the expression of an altered penicillin-binding protein PBP2a, which resists inactivation by beta-lactam antibiotics, in methicillin-resistant Staphylococcus aureus (MRSA). BlaR1 regulates the inducible expression of a class A beta-lactamase that hydrolytically destroys certain ?-lactam antibiotics in MRSA. Both, MecR1 and BlaR1, are transmembrane proteins that consist of four transmembrane helices, a cytoplasmic zinc protease domain, and the soluble C-terminal extracellular sensor domain, and are highly similar in sequence and function. The signal for protein expression is transmitted by site-specific proteolytic cleavage of both the transducer, which auto-activates, and the repressor, which is inactivated, unblocking gene transcription. All members contain the zinc metalloprotease motif (HEXXH). Homologs of this peptidase domain are also found in a number of other bacterial genome sequences, most of which are as yet uncharacterized.	4.0079e-53
NZ_CP017169.1\|WP_140786655.1\|223843_225280_-\|VWA-domain-containing-protein	gnl\|CDD\|238742	cd01465, vWA_subgroup, VWA subgroup: Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains. Not much is known about the function of the VWA domain in these proteins. The members do have a conserved MIDAS motif. The biochemical function however is not known.	6.43083e-34

>NZ_CP017169.1|WP_140800574.1|216970_217381_-|fibril-protein
MLFLAACASTNKSAVPEPRASASTAPRVEVVEYGFHPQDPVRVGWGDRGMMAFLELLRGPQGQRIAWRRVGPCCGAGAPTELEVFEVTYDGLAAPVSLYLDPNTAGAVHAPNGFSIQGLASRSQVEQEETPRVIEL
>NZ_CP017169.1|WP_140796922.1|215030_216962_+|DUF885-family-protein
MRDSRPPRTPRRTRMGTFSRQLGRELFDGESSRPRFPLSEPPFNHETRRAMRIRSAFVLLACVSACASRSGAGPESSTAMPTASVSAADADYVLLAREYLDWYAAANPTRATRLGYHMHDAHLPDVSSDALKRKAEALRGWLTRLEQAVARGGLSGDAAVDVRVLENAMRADLLELEEVRPWERNPGFYVGIISSGLDGLSSREFAPVAERMRAMRSRMARIPGVLDAAQFNLSGVPKLWAEYALRDARGTVAYLRTDLPRALAAQGYAQVPLSERAAFSAAREEAARQMEAFAVWLERELLPKADGDFRLGRERFEKKLALEEHVTLDADALRDINERAIRDYKAWVAREAARLDASKTPEQVMAELVKDHPKAEELVASARAQLVELQRFVRERNILTLPSDRLPVVRETPPYARLGFASMDTPGPFETKATEAFYNITNVEPGWTPEQKAQHLTYFNRAGLLGITVHEAMPGHFVQLLYGARIPTDVRKVFTPASLVEGWAHYSEQMMVDEGLGNGDPAVRLGQLRRALQRHARWYAALALHVYGEPVEAVAKRYAEIAYFEPFPALREVERGTLDPTYLYYAVGRMQIFKLRDDYRRHLESRGKTLVLKDFHDRLLQLGLPVSLAREVFLPGDTAPSLE
>NZ_CP017169.1|WP_140852807.1|212567_213269_-|hypothetical-protein
MSMHWTGRASCWRRWDREANRIAGGAVLTLALSCSGNLRHAQETESYGFMSIDSGYVWARGPWPEVQASSDPDEVIDQLCPAIMRLDRATARDFGQEYCGVIYSRGDGIYRTTHPSPLGEPQLRGETKQKSCFPVRRVVDPEAKVTPILADFHSHPWFPSPLSQQDKMAANQLYFLKIQFDSACQIQKIIPYLDRPDAPGEVYSRRGKRWVLIGIIKPSNKAAGIVPPVGGLD
>NZ_CP017169.1|WP_140796920.1|212135_212555_-|hypothetical-protein
MTRWLPFLILALPACALFQRPPRPVHAPPEEAARFAFPPTGIPEEGLRSIPGDMARAIQLAMEDFYPWDKKVPTPSHPGRECLYRRESYDVYAAPYQEGVVLVSIVLSPQACGAQAVPNDMGALYAVDTRGWRILAVQH
>NZ_CP017169.1|WP_140852806.1|209068_211771_-|AsmA-family-protein
MSDTVVKKKRRWPYVLGGVFALLVIVVAVALWRLDAILLKTARDQAATYSQLLGRPIEIGDISTKLFPTIGAQVENVTVGPAEGEDLPLAQLALIDVRVAAGPLLSSSGKDIQVKNAEVSGLTVNLVRFADGTTNVQRLLQRLEEQQPKEEEAPAEESQPMDLSGVHVERAALTDGAIRFVDRGAGAQARELGVKDLDIEVKDLRVGKPLVVNLAAAVLADTQNLQVSLHAAPLPATLVPMPERVTLKAQKIDLAPLGPFLPPDIGLQAGTLDADWQADLGGAVPGGQGPTKLVGIIKALGLSFTGSEGGKALDVVMDTDVAGDITTGDLALNKLKVDLGPASLTGKGSVKGLLTDKPAVEGFELTGRNLDPAALAEYYPPLRKQLNGMIAGPIGLDVRGSGTQDAQAIDVNVDLTPVRLRVPAQLTKDAGGAMKLSARVSGAAATGGALRFDAKADLGGIDLRPGLLVDKAPGQRMDLSAAGTYAPGKGSGMKVDIPKLTANVLADTMTGSASFALAGSGKKQTTTFSADLKSQKLDADALMMSEEEVQARGGPPPEEPPSDDPTRFNGYRGDIRFAVGTLRYMEMNMTNVTGVVKMTDDLIAVEKFSTGVYGGRIVADGTTVRLGPLPEQRPFEAKVKVEGVAVEQALTQFTPQKAVTGKFNGNVDVKGVGYTPDQLKQTLLGGINGDLLDGELLGKDLVSAVSEPLAKALPIAAKGLKNEQVTKLGGDLPFSVQIKNGVAQLSKPLTWSRPEAELSFDGGIRLDGALDLTGSVSLSPSTVKTLTLGKVTPPAAIPVGLKLTGPAWKPEVTSLDVKPAVTQIAKLAASSLAGNLIGGERGQQVQGLIEGGEDKLRAEAEAKRRELEAKAAEEKARLEAEAKKRAEEEAKKRLRGLFGK
>NZ_CP017169.1|WP_174259028.1|207646_208861_-|NAD(P)/FAD-dependent-oxidoreductase
MVPVREHHRVLIIGGGTAGIAVAARLARAGQKGVAVLEPSQHHYYQPLWTLVGAGEARIEDTVRNESRLIPRGVKWVRDAATEIDPEAREVLTRGGLRLGYDFLVVAPGIQLDWDKVAGLREALKTPHVSSNYDVQLAPKTWRLLQNFQGGTALFTQPSTPVKCAGAPQKIMYLAADHFRRTGVLERTSVVFGSGAKTIFGVKPFASVLEGVVHRYGITPRFQHNLIAVDGERREATFEAPRDGQTERITLAYDMMHVTPPQSAPDFIKRSPLSWQEGPNAGWVKADKYTLQHPDHPNVFALGDASDLPTSRTGAAIRKQAPVLVENLLACMKDLPLPARYDGYASCPLTTGYGRLLLAEFDYDGKPAPTIPFIDTMQERRDMWLLKKYGLPRLYWAFMMRGLA
>NZ_CP017169.1|WP_140786644.1|206330_207617_-|sigma-54-interacting-transcriptional-regulator
MPTSHLALPALDALAGPVLLVDDARKVTALTPALEALLGGTLRAGTPLAQVLVRADGTEPLDAVLKNGREASVRLRVGGRSKPVRVRAVPLARGPRASGWALLLSPDAEEETNGRAELFHGLWTQAPELQRVFRIVEKVARTESSVLVRGESGTGKEHIAHALHALSARARGPFRAINCAALPPNLLESELFGHVRGAFTGAVRDSPGHFRLADKGSLFLDEVAEMPLDLQAKMLRVLETRTVIPVGGRQPVPVDVRIIAATHRPLRREVEAGRFRADLMYRLRVVPLFLPTLRERRGDILPLALRFLEELHQRGARRVERFSPGARRLLEEHPWPGNVRELRNVMEYAYVIGEGPVVREADLPPEFSEPRQAIPVTQPPLDASLEPERIRAALAQAGGNRSEAARLLGVSRVTLWRRLRDLGASVER
>NZ_CP017169.1|WP_140852805.1|205383_206088_-|MBL-fold-metallo-hydrolase
MLFRQLFDADTSTYTYLLADEATGAAALIDPVLEQTERDLKLLRELGLTLSVVLETHVHADHVTGAGVLRERTGATVVASTRGAPCVDQTVHHGDIVRVGGLEVRVLETPGHTDDSLSFLCERRLFTGDALLIRGTGRTDFQNGDPGQLYDAITRVLFTLPDDTVVYPGHDYAGHAVSTVGEEKQHNPRLAGRTRADFIVLMNALQLPPPRKLDVAVPANRACGHTPPSPSLQA
>NZ_CP017169.1|WP_140852804.1|204754_205366_-|rhodanese-like-domain-containing-protein
MHPLFDNATPHPAGYRDVDVGQLAACLPSELTLVDVREAAELDGILGHVAGIRHAPLATVPDVVDTWPRDTDVVLICRSGARSARAATSLVTLGFTRVMNLRGGMLAWNTARLPVVRPVPHTLPTLGTVRDGLLDGLHRALTPPPHEAPTVPPMTTPSREALTAVLDALQAARPTDVRDAAAFEHLLRTYRDLLAAARAEGER
>NZ_CP017169.1|WP_140852803.1|203876_204758_-|TSUP-family-transporter
MMLYAGIAGSLLVGILLGLLGGGGSILTVPLLIYVLDVEPRTAIAMSLVVVGVTSASGAFLHARAGRVRWRTALVFGTGGMGGAFLGGRLNPHIEPDTLLLLFAGVMVAAAVAMLRRREAGPVSTSVSPLPAPRVLAQGIAVGVLSGLVGAGGGFLIVPALSLAGLSMPVATATSLVVIALQCAAGLVGHLGHLDLPWMLTGEVLLAAMTGSLVGGRLAGRVPPALLRKGFAVFVLTTAAFILSAQAPAPLRERVWTEGLWLWSVAPLAVGIPVTVWRLRVARQRQTAQALPR
>NZ_CP017169.1|WP_140852808.1|218612_220736_-|M56-family-metallopeptidase
MSRLLMESLGWALLHSLWQGTLVALMLAVALITVGRRAAHARYALACGALVLALALPVASGWKHFHGAPARVAMDLSVPRAQLRVDDANPPPVKDTAARPAWRLSPVAASPAWIDADMAEDGAASGFESTVLTGLGSFLVMAGLLLQRALSQVEAHLHWLVLAWVAGVGLCSGRMAAEWMKLRRLADRALPAPEAWQERLDALSRRMGLRRAVRLLQSSDVDVPAAVGWLSPVVLLPVSTLSGLPARQLEMVLAHELAHIRRHDFAVNLAQVLVETLLFFHPAVRWISHVIRVEREHCCDDVAVAASGNSVSYARALTALETLRVLPGTPSPAMSALGGSLPERVRRLITLPTSRCASRWAAGASVLTLVSSLAVAAPLTSLLLGQTDTAPRPGDEPVLVQAPPIPALSRTPPVPPAPLPVAPPAPPAPPAPPAGVAAVAARVAPAPAPSPAPQARSLGSRAQRELDRQTRVGAGQQLSVAQLIALKNAGITPERVQQLTAMGYTPTVSNLVMMTHAGITPDYVQDMNTRFGRKLEVKELTHLRHLGVTPDYIQSLKSAGFNIDDPKALSHARAVGVDEDFVRGLKDAGYTGMSLEELAHLRAVGVSPEYIREMNKHGLSKLKARELMQLRAVGVDPGWLASMRKAGVQTTDAKALQRLRATGVDADFLGELHDAGLKDLSVDELVRLRTGGVDADFIRKMRGTDSK
>NZ_CP017169.1|WP_026113917.1|220732_221128_-|BlaI/MecI/CopY-family-transcriptional-regulator
MSETKLPRPTDGELAILRVLWARGDSTVREVHEALTRDEPEGTGYTTVLKLMQIMTEKGLVERDESQRAHVYRPRATEQRTQRQLVTDLVDRAFGGSPARLAMQALSSKKTRPEELAELRRLLDTLEGGEE
>NZ_CP017169.1|WP_140786652.1|221277_222093_-|sterol-desaturase-family-protein
MAVSAPFSFLKNRKHNLDRMTLGDLVYSFFTYYAVVAYITVGIISLALAVKWFENPLRMLLAMLAASVAFPFGWYLVHKHILHSRFLYKSPLTAATWKRIHFDHHQDPHDLRVLFGALANVLPTVGGVIAPIGYLIGGKAGAAAALGWAMVITCFYEFCHCIQHLNYTPKSQFLKDIKRLHLSHHFHNEQGNYGITNYFWDRLFGTFYEKSGDKPKSPTVFNLGYTAEEAQRYPWVDRLSGGTRGDGHPRRFWEDQAAAQTPPEPTTRQDS
>NZ_CP017169.1|WP_140796924.1|222371_222716_+|hypothetical-protein
MTFREARMAEHEGQQTPRTKVRRRRTSTPKAVRTGERSAGPDRGSIALRRTASEYRATAEEQAARVREEIEAALVQARSTREAIEQRIADQLHAPPVRHTPPPRRKRATRASRK
>NZ_CP017169.1|WP_140796925.1|222724_223828_-|hypothetical-protein
MALSVQYFHREEFETRTLRALGGAACMGLVAGAVPDLHLTPEYVAIVAAAQACVKPTGVHPLALRLALTVLPALPYFFRAPEPLPVSLAGALAAALVAWLGHGREQPGQPAAVATSAAAAGVLVPLGLYVQQVLEARFLGSDGLLSALVGFLVVGLFWSIGTLPANLRVELDAVEARGRQLQDALKGDSRTLATRALTLYRQCKDVVTKMPPSTGRTELLGVLEKMTGDSFSLAEVHFGLEAQLGSVVANDVDAQVRELRERAAATQDAVARRQLELAASSLGEELNHLDVLARRKERLLAQLHAQVAMLERARVSFIGVQGNELGAKGAQAADLARKLKQLGEPASSAGPEDVAPVAAPNPTRVAP
>NZ_CP017169.1|WP_140786655.1|223843_225280_-|VWA-domain-containing-protein
MNRSLLLVAATGVLAVGALLLGTPPTPPGPPPPAVTDTSHTVRRPEDPPATRTLTLVTSKPEDGALNMAGKLSGAYVQTGPSEAFAWLELKARPAETGQRVPVSLALVLDRSGSMNGQKLADARRAATELVQRLKPEDRLAFIDYGTDVRVQPSRRMTEEAREELLTLISGLQDDGSTNISGALDAAANALRPHMREYRVSRAILLSDGQPTTGIVSEPGLLDQVRQLRRDGITVSALGVGRDYQETLMRGMAEQGGGFSGFIDDSARLAEVFSRELDQATSTVARLVELRLDVPPEVQHVEVMGMASFREGNVLKVPLYDMASAQTVRIMAKLTLNTPRTTGALALLNARVHYVDVARDMPTETALRLTAEVTSDLDLVREHLDKEVRVHATRALGTQHMVAAAEEMKRGNKAKARSLLDNARTIFGSSADALSGELADVNRSQAALAGASSAEEAQAESRNLLKKSIKNFGQNNTY
>NZ_CP017169.1|WP_174258588.1|225393_228252_-|PAS-domain-S-box-protein
MQKPHSTPDWTSREHRYRGVIDSLREVVFQTDLAGTWTFLNPAWTDITGFSVEESLGRSFSDFLHPDDRERDPEPLQKLFAGEVEFVRHEMRYLTRDGSYRWVEVFARLMHDDDGGILGTAGTLNDFTERKAADGALARRERYLTALVDMQQRLLATQDGGDLYGPALAPLGHASGASRVYVFELHRAQDGAVLSSQRAEWCAPGVKPEIDNPDLQNVPMEPALRRWTETLSRGDVIEGLVESFPAPERELLEPQGILSLLVLPLRVRGVLTGFVGFDNTSEARRWDRLEVDLLSAAAGAISMALERRESERALRERERRFRQLAENASDVLYVYRREAPRGFAYVSRVAHTKLGYGPVAHYADAELWYRRVHEEDRALMEQLLEAPEPFQGAPVVVRFLHPDGRTLWLEHVVAPVTDASGRMVAVEGLARDITVRRQAEEALRLSEASFRALLEGVPDAAAIERDNQIVYANAALVATLGFERADQLVGRPLTEFVRDMRSPDAVRAGALTGERRLVRRDGRTRVAEVVSLPLRFDGQPAVVSIARDVTEQRQLQARLTLADRLASVGTLAAGIAHEINNPLAFVLSNLGFLSDEFNRSLPPGDGAAALQARLKGEPDLGEWQEVLQEACEGAERVRQIVRQLKTFSRPDEERVSPLDVHAVLESVAMMAANEIRHRAQLRRDYGDIPPVMANEGKLSQVFLNLVVNAAQAIPEGAAHRHEIRLATRVDGAGRVVVEVADTGVGIAREVIDRIFDPFFTTKPVGVGTGLGLSICHSIISGLGGDITVDSEPGRGTLFRVVLPTPETVERAKPSEPDSRQAPHAPRGRVLVVDDEPAVGRVLQRILREHQVDVACSGRQALELLERGLAPDAVLCDVMMPDLTGRDVYEAVRREYAGLERRFVFVSGGAFTSGARDFLASIPNMLLEKPFDEARVRGVVEELVRQRQPAHDA
>NZ_CP017169.1|WP_174258589.1|228485_230210_+|GAF-domain-containing-sensor-histidine-kinase
MASGSAPLSMTHLDSEEADALLKEGVLRLLLEQAGEALVLVDVTGRVLAFNVEAGRQFRMSRPERAEQGWLPGCVWTRAEDASMSVEVPPLARALTGEWVAEARWRVRRPDGTHVLLRASAVPLEHDEGPTAGALLRACEVASSVGLDAVGSARLLAEAGALLGAAFDDEAAPRLLRLLVPALADAAVLYLGLPGGPPRPVTALHAEPERHGLLEEALRRYPLPPERVLPLFGTGQSERLRVTEAHVEAAARDAEHARLLRGLGLRCYLGVPLVARERVIGTLALFRADEARDFSVEELRLAEEVARRTALSVDNAQLLQEAREAVRLRDEFLGIASHELKTPLTPLHLKVQLLQKQVDGMAAHNQPVSAERVSETLEVVQRQVRKLTSLVDNLLDVSRITAGRLRLEVEEMDLASVAAEILYRFAPSASQLQCELELHAPVPVMGRWDRLRLEQVVTNLLSNALKYGAGHPVRVAVEAEGLTARLTVRDGGIGISAEDLPRIFERFERAVSDRHYGGLGLGLYITRQIVEAFGGTVRATSEPGQGSLFVLELPRGDIPEEWLTAHGAPEPSSS
>NZ_CP017169.1|WP_174258590.1|230214_232731_-|HAMP-domain-containing-protein
MSSSPSPQIQAPSPPALLPLTWPAAVVGLMFGVLMTYVPYEFRVASFRPLYPYVRVLGLTYLTGSIMLMGALLYPRAPRWLDVTGRLLLGAAMALYWWVLNVLPGSFTGIILYPVLFGGVVLEAWPAMRQRPVLRTFAALTGAAFGVAMLVVPERFPLSVYAHLAPLRPLVGLLFAVCGVGLLLPSHRLHRQLPALFMGGLAVPFALLAYALGRGASWLGASVYAVLTLACVAQALDWRPRAPRTVGWKLLRGLAFAGLVPLLALGGLAAYLAQNAIEQQVRDDTQRAAAGEADFLRRYLDDAGESLALMLESPGFRAAFAAAAPERLEPYLVNLAAQERAFDAALAVDTQGHILAASPSVEGWNLEPRDFLPPAFTRGAEVSPPFIRPPGQPLVAVTQPFREDGEVRGMLVGLLSLERLSQATTPASRRFRVQVLDRRGLKVLRDTAPGAPLLGEAHLPDALSLELLRPGIGVLEAFDAADRRMLAAEAPVEGTEWSVLVTQELVVAYAAITRMSAAVVGLVLLGVLMALLLSQLVARDVIRRLDHLRTATAALTAGDWSQRVDVEEDDELGELARGFNEMAARTGATQTELKEAVRAREEFLSVASHELRTPLTPLKGFAALTLQRLEKSGDFPERERLLKALRSMARQTERLTRLVDDLLDTARIQGGRLELERKRMDLAPLLGEVLERFELRTESGVTFELDVPSHPVEGDWDALRLEQVLTNLVSNAVRYSPHGGAVRMSLEAAETHVLLSVRDEGIGIPPENVADLFRPFARASNAQARHFGGLGLGLFICREIVERHGGAIWAESPGPQRGSSFHVRLPRRAEPAASASAA
>NZ_CP017169.1|WP_140852811.1|232801_233317_-|GreA/GreB-family-elongation-factor
MRLDKHALLGQLADRLQQSDRLAHRAEAEAREAARSLATESEKKEDGRAALEFGSLATGQAQRARRVQEELQALTKFGQAEFPRFPRQGPVALGAIVDVSTEDEEGFSERTFFVLPAGAGTELTGPGGDGFLSVITPASPVGRALMGRKAGDTVEVILAGEVREWTVLEVA

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Crispr_ID: NZ_CP017169_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_2

654712-654804

Orphan

Consensus_repeat	Method
CCCATCCCGCGCCCGCGCCCGGAGAACCTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_2

>merge|NZ_CP017169|2|654712-654804|CRISPRCasFinder
CCCATCCCGCGCCCGCGCCCGGAGAACCTCACGGCGGGCACCACGGAGCTGCCCGCCGAGGTCCCCATCCCGCGCCCGCGCCCGGAGAACCTC

>NZ_CP017169|2|2|654712-654804|CRISPRCasFinder
CCCATCCCGCGCCCGCGCCCGGAGAACCTC	ACGGCGGGCACCACGGAGCTGCCCGCCGAGGTC
CCCATCCCGCGCCCGCGCCCGGAGAACCTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_162521002.1\|666342_666681_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274743
NZ_CP017169.1\|WP_140852952.1\|649463_649709_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140787005.1\|647729_649409_+\|energy-dependent-translational-throttle-protein-EttA	unknown	unknown	gnl\|CDD\|236992
NZ_CP017169.1\|WP_174259031.1\|652279_653620_+\|porin	unknown	unknown	gnl\|CDD\|369347
NZ_CP017169.1\|WP_140787025.1\|663139_665404_+\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_140787021.1\|658224_658416_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140800596.1\|662459_662933_+\|thermonuclease-family-protein	unknown	unknown	gnl\|CDD\|366169
NZ_CP017169.1\|WP_140852951.1\|646655_647120_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380436
NZ_CP017169.1\|WP_140787017.1\|656735_657308_-\|TIGR02265-family-protein	unknown	unknown	gnl\|CDD\|131318
NZ_CP017169.1\|WP_140787027.1\|665481_666312_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140858155.1\|660648_662460_+\|lamin-tail-domain-containing-protein	unknown	unknown	gnl\|CDD\|376421
NZ_CP017169.1\|WP_140787003.1\|647164_647497_+\|DUF2834-domain-containing-protein	unknown	unknown	gnl\|CDD\|371414
NZ_CP017169.1\|WP_140787009.1\|649723_650632_-\|peptidoglycan-binding-protein	unknown	unknown	gnl\|CDD\|350624
NZ_CP017169.1\|WP_140786996.1\|643131_644064_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP017169.1\|WP_140787010.1\|651162_652080_+\|protease-HtpX	unknown	unknown	gnl\|CDD\|235478
NZ_CP017169.1\|WP_140852955.1\|658498_660622_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140797094.1\|644187_645018_-\|metallophosphoesterase-family-protein	unknown	unknown	gnl\|CDD\|277322
NZ_CP017169.1\|WP_140787019.1\|657318_658092_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225375
NZ_CP017169.1\|WP_140852950.1\|645124_646552_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|224089
NZ_CP017169.1\|WP_174258623.1\|655566_656730_+\|ATP-grasp-domain-containing-protein	unknown	unknown	gnl\|CDD\|223516

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_162521002.1\|666342_666681_-\|hypothetical-protein	gnl\|CDD\|274743	TIGR03718, R_switched_Alx, integral membrane protein, TerC family. Rfam model RF00080 describes a structured RNA element called the yybP-ykoY leader, or SraF, which may precede one or several genes in a genome. Members of this highly hydrophobic protein family often are preceded by a yybP-ykoY leader, which may serve as a riboswitch. From the larger group of TerC homologs (pfam03741), this subfamily contains TerC itself from Alcaligenes sp. plasmid IncHI2 pMER610 and from Proteus mirabilis. It also contains the alkaline-inducible E. coli protein Alx, which unlike the two TerC examples is preceded by a yybP-ykoY leader.	3.25991e-21
NZ_CP017169.1\|WP_140787005.1\|647729_649409_+\|energy-dependent-translational-throttle-protein-EttA	gnl\|CDD\|236992	PRK11819, PRK11819, putative ABC transporter ATP-binding protein; Reviewed.	0
NZ_CP017169.1\|WP_174259031.1\|652279_653620_+\|porin	gnl\|CDD\|369347	pfam07396, Porin_O_P, Phosphate-selective porin O and P. This family represents a conserved region approximately 400 residues long within the bacterial phosphate-selective porins O and P. These are anion-specific porins, the binding site of which has a higher affinity for phosphate than chloride ions. Porin O has a higher affinity for polyphosphates, while porin P has a higher affinity for orthophosphate. In P. aeruginosa, porin O was found to be expressed only under phosphate-starvation conditions during the stationary growth phase.	1.52699e-24
NZ_CP017169.1\|WP_140787025.1\|663139_665404_+\|PAS-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	8.09189e-44
NZ_CP017169.1\|WP_140800596.1\|662459_662933_+\|thermonuclease-family-protein	gnl\|CDD\|366169	pfam00565, SNase, Staphylococcal nuclease homolog. Present in all three domains of cellular life. Four copies in the transcriptional coactivator p100: these, however, appear to lack the active site residues of Staphylococcal nuclease. Positions 14 (Asp-21), 34 (Arg-35), 39 (Asp-40), 42 (Glu-43) and 110 (Arg-87) [SNase numbering in parentheses] are thought to be involved in substrate-binding and catalysis.	1.31205e-20
NZ_CP017169.1\|WP_140852951.1\|646655_647120_+\|cupin-domain-containing-protein	gnl\|CDD\|380436	cd20302, cupin_DAD, 2,4'-Dihydroxyacetophenone dioxygenase (DAD), cupin domain. 2,4'-Dihydroxyacetophenone dioxygenase (DAD) catalyzes the oxidation of 2,4'-dihydroxyacetophenone to 4-hydroxybenzoate and formate as part of the 4-hydroxyacetophenone catabolic pathway. This enzyme is a homo-tetramer containing one iron per molecule of enzyme. This enzyme is an unusual dioxygenase in that it cleaves a C-C bond in a substituent of the aromatic ring rather than within the ring itself. As a bacterial dioxygenase, DAD plays an important environmental role in the aerobic catabolism of aromatic compounds; expression of this enzyme in appropriately engineered microorganisms has the potential to use these aromatic pollutants as a carbon source and thus remove them from the environment. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.44789e-31
NZ_CP017169.1\|WP_140787017.1\|656735_657308_-\|TIGR02265-family-protein	gnl\|CDD\|131318	TIGR02265, Mxa_TIGR02265, Myxococcales-restricted protein, TIGR02265 family. This family consists of a set of at least 17 paralogous proteins in Myxococcus xanthus DK 1622. Members are about 200 amino acids in length. No other homologs are known; the function is unknown.	1.10142e-70
NZ_CP017169.1\|WP_140858155.1\|660648_662460_+\|lamin-tail-domain-containing-protein	gnl\|CDD\|376421	pfam00932, LTD, Lamin Tail Domain. The lamin-tail domain (LTD), which has an immunoglobulin (Ig) fold, is found in Nuclear Lamins, Chlo1887 from Chloroflexus, and several bacterial proteins where it occurs with membrane associated hydrolases of the metallo-beta-lactamase,synaptojanin, and calcineurin-like phosphoesterase superfamilies.	6.45006e-09
NZ_CP017169.1\|WP_140787003.1\|647164_647497_+\|DUF2834-domain-containing-protein	gnl\|CDD\|371414	pfam11196, DUF2834, Protein of unknown function (DUF2834). This is a bacterial family of uncharacterized proteins.	4.90953e-18
NZ_CP017169.1\|WP_140787009.1\|649723_650632_-\|peptidoglycan-binding-protein	gnl\|CDD\|350624	cd14852, LD-carboxypeptidase, L,D-carboxypeptidase DacB and LdcB, and related proteins. This L,D-carboxypeptidase family includes LdcB LD-Carboxypeptidase from Streptococcus pneumoniae, Bacillus anthracis, and Bacillus subtilis, and L,D-carboxypeptidase DacB from Streptococcus pneumonia and Lactococcus lactis. These enzymes are active against cell-wall-derived tetrapeptides and synthetic tetrapeptides lacking the sugar moiety but are inactive against tetrapeptides terminating in L-alanine. L,D-carboxypeptidase DacB plays a key role in the remodeling of S. pneumoniae peptidoglycan during cell division. It adopts a zinc-dependent carboxypeptidase fold and acts as an L,D-carboxypeptidase towards the tetrapeptide L-Ala-D-iGln-L-Lys-D-Ala of the peptidoglycan stem. This family also includes vanY D-Ala-D-Ala carboxypeptidase which is vancomycin-inducible and penicillin-resistant. VanY hydrolyzes depsipeptide- and D-alanyl-D-alanine-containing peptidoglycan precursors; it is insensitive to beta-lactams. All these enzymes belong to the MEROPS family M15 subfamily B.	3.06266e-32
NZ_CP017169.1\|WP_140786996.1\|643131_644064_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.53387e-94
NZ_CP017169.1\|WP_140787010.1\|651162_652080_+\|protease-HtpX	gnl\|CDD\|235478	PRK05457, PRK05457, protease HtpX.	4.91805e-171
NZ_CP017169.1\|WP_140797094.1\|644187_645018_-\|metallophosphoesterase-family-protein	gnl\|CDD\|277322	cd00844, MPP_Dbr1_N, Dbr1 RNA lariat debranching enzyme, N-terminal metallophosphatase domain. Dbr1 is an RNA lariat debranching enzyme that hydrolyzes 2'-5' phosphodiester bonds at the branch points of excised intron lariats. This alignment model represents the N-terminal metallophosphatase domain of Dbr1. This domain belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	7.3049e-45
NZ_CP017169.1\|WP_140787019.1\|657318_658092_-\|alpha/beta-hydrolase	gnl\|CDD\|225375	COG2819, COG2819, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	3.9375e-37
NZ_CP017169.1\|WP_140852950.1\|645124_646552_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	4.69889e-147
NZ_CP017169.1\|WP_174258623.1\|655566_656730_+\|ATP-grasp-domain-containing-protein	gnl\|CDD\|223516	COG0439, AccC, Biotin carboxylase [Lipid metabolism].	1.11878e-10

>NZ_CP017169.1|WP_174259031.1|652279_653620_+|porin
MTPTASFRAALQVLLSGSALLLAPLAHAQQDEAAPSSATETPPASEPTPTPTPVPEAAMPEPETKPEAEKKEQAWYDRIRIRGYTQFRYNRLPSFRVNDELVNDQGDRFLGKNTGFGIRRARLVLFGDVSDRVSIYLQPDFASVIGDQYNVTIMRDWYADIFLDAKKEFRLRVGQSKVPFGFENLQSSQNRVPLDRNDGINSGLKDERDLGVFFYWAPDEIRKRFKFLVDNNLKGSGDYGVVGFGVFNGQTANRAERNDTPHGVVRVTWPFLFGSQYVEAGVGGYYGRFDLTASPRDGAPYALARGSNMVDARAIVSLVIYPQPLGFQAEFNLGRGPSLGEGPVDGLLIDSRQLRGGYAQLMYKLDGVLGVSLIPYIRGTLYDGGKKFETNAPLYDVRELEMGAEWQLNKVLELTGTYLISDRTSSRYPYIQQQGHVTRVQLQVNY
>NZ_CP017169.1|WP_140787010.1|651162_652080_+|protease-HtpX
MKGSFAKRITLFVLTNLAVVAMLAIVGQLIGVENLLARRGVGLNLPGLLIMAAVMGFGGAIFSLLISKPMAKWSTGAKVITSPRSEDERWLLETVHRLARDAGIGMPDVAIYDSPDMNAFATGAKRNSALVAVSTGLLHGMKRDEVEAVLGHEVAHVANGDMVTLTLLQGVLNTFVIFLSRVVGFFVDRFLSRSEDGEESGGSGPAYFITSIVLQIVFGIGASMIVAWYSRRREFRADDGGAQLVDPGAMARALNRLRMQQGEPAMLPSNMQAFGIRGGGMMALFSSHPPLELRIQRLMDGSWKS
>NZ_CP017169.1|WP_140787009.1|649723_650632_-|peptidoglycan-binding-protein
MVAIARSSAAASSSASRSASPTLRSGARGAAVTQLQNKLRAAGFNPGAADGVFGPKTQAAVQSFQRARGLQVDGIVGPKTWSALNSAGGTGGSGPTLRNGARGEPVRALQQRLNVLGFKSGTADGAFGPKTLSAVKAFQQSRGLVADGIVGPKTWDKLGINVQGPVTNPGGGGGGRVVTGYVNGQPRQISLSSVPNGKEMRSDAAAAYNRMYAAARAQGITLKVNSGFRSMGEQEALYRAYKNGTGNLAAPPGYSNHQGGIAVDVNTGGTGTSTYRWMANNAKNFGFVRTVPSEPWHWEYRP
>NZ_CP017169.1|WP_140852952.1|649463_649709_-|hypothetical-protein
MKKLLMAFAVLAAPAGVVVGGLGYTPVAEAESLNQACTYTYYNDEALTEYVMTLHCSCANPDCYNTEDVTPFYTVDCIHSC
>NZ_CP017169.1|WP_140787005.1|647729_649409_+|energy-dependent-translational-throttle-protein-EttA
MAQNFIFTMQDLRKVKNGKEILKGIYLSFFPGAKIGVIGPNGSGKSTLLRIMAGVDTEFFGVAKPDPSAKVGYLAQEPQLDASLDVKGNVELGLKEIRATLDRFNEVSAKFAEPMSDAEMEKLLAEQGRLQDAIDAVNGWELDRTIEMAMDALRLPPGDADVTKLSGGEKRRVALCRILLEKPDLLLLDEPTNHLDAESVAWLEQALKEYKGTIVCITHDRYFLDNAAEWILELDRGEGVPWKGNYSSWLEQKQKRLELEEKSESHRQKTLKRELEWVRASPKARQAKSKARIAAYEELLNQTQDKRDATGEVIIPPGPPLGGLVIEAKGLRKAYGDRLLIDDLSFKLPPGGIVGVIGPNGAGKTTLFRMMTGVESPDAGELRIGETVKLAYVDQSRDALDGDNTVFQEVSGGLDHLDLGKAGQVPSRAYLAGFAFKGQDQQKRVKDLSGGERNRTHLAKMLKSGGNLLLLDEPTNDLDVETLRSLEDALLSFAGCAVVISHDRWFLDRIATHILAFEGDSKAFFFEGNFEDYEADKKKRLGPEALEPHRIRYRPITKS
>NZ_CP017169.1|WP_140787003.1|647164_647497_+|DUF2834-domain-containing-protein
MKTRHLKSVLLALTVAGVAIPYAAFVPFVVEHGLDVPLFVAQAAANRISAFAWLDVVVSAVVLLVAAYSGRFIQRNQALFVTGLTLGAGVSAGLPLFLYFALDAGAFKRD
>NZ_CP017169.1|WP_140852951.1|646655_647120_+|cupin-domain-containing-protein
MNDTSSSSASSRPVDPERMPWIPMGPAGLSFKPLRFFRDGSGWMYLFRLEPGTVIPRHRHTGEVHGFNLSGTRELLDTGEVIGPGGYVYEPPGNVDSWRVTCDAPVVLLITVRGAIEYLTEDGQVSKRVTSEDRLQTYRRWCEANSAPFMATLE
>NZ_CP017169.1|WP_140852950.1|645124_646552_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MDLHVDLQDRRDVAGQIYRGLRARILDGRLRDGEQVPPSRELAQRLGVSRNTVGVAYEWLAAEGLLVGRGRAGSFVQNAPRDQCARAAATRGVKLRPRAVWSELHVPPPAEPPAPYDFRVGTPDAALFPFETWHRLLARHLRAAVMTAAYADPAGHPELREAVARHVGVSRGVRAEASDVLITHGAQQALDLAGRVLLEPGDRVAVEEPGYPPARLLFQSLGARVVPVPVDEEGLDMQALPDDTRLVYVTPSHQFPLGIVMSPARRRALLDWARRRDAVVIEDDYDSEFRFGGRPLETLHSLDRSGRVLYVGSFSKVLLPALRLGFLVAPPSLQREFRLAKQVTDWHSQLPAQAALARFIDTGALARHLRKTRREYEQRHTRLSEKLRHHFEDAFEQLPSVAGLHLCVTFTRGGARLERELTRRARDAGIGIEALSGYFAGAPTRHGWVLGYGGVTVDRIDEGLRRLRTRLAGAL
>NZ_CP017169.1|WP_140797094.1|644187_645018_-|metallophosphoesterase-family-protein
MSSSQTFFFAVVGDVHGHMHRMVSHLTAWEERSRRPLDFVLQVGDFEPHRHDADLVTMAAPMKHRHLGDFEAYHQRRRRFPWPVYFIGGNHEPYGHLDLYPEGFELAPHCHYLGRSGVVELNGLRVAGLSGIHREATFCKSRPPLASMGDVSNKDFTFFNEQDVERVLALGRADVLLLHDWPSGIIPPEEAADFQGQRRSASHDLVGNAYARLLVDALQPRLVLCGHLHRPYAGTVQHPGGQRSLVRCLASVEQGADAFAVFQCREGTLQEVAMRE
>NZ_CP017169.1|WP_140786996.1|643131_644064_-|ATP-binding-cassette-domain-containing-protein
MSVPALELQGLSKRYGEFTALHTVDLAIRPGEIFALLGPNGAGKTTMIGSVCGLVKKSSGSIRVFGKDLDQDPVGPRYDIGLVPQEINFDPFFTVAESLRIQLGFYGRPADDARIDEVLTALNLHAKKDAYTRALSGGMKRRLLIAKALVHKPRLVFLDEPTAGVDVELRRDLWTYVRKLASEGTTIVLTTHYLEEAEELADRVGIINEGRLLMVEDKATLLRRFGERRVIITFEQPQPGLSEAGKRFTARLSEDGRTLTYVERDGCAPSGELLRALYAEGQLISDVETRRSRMEDVLIEILRGRPQQAA
>NZ_CP017169.1|WP_174258623.1|655566_656730_+|ATP-grasp-domain-containing-protein
MNFVFISPHFPPHYFHFISALRERGVTVLGIGDASYESLRPELKESLREYYFVPSLMDEDALTRAAGYLTWRHGRIHRIDSLNESWLEVEARLRGDFNVPGLQPADIHRLRSKSGMAEVFQEAGVPHPDLIRVRDAAQVKAFAARVGYPLVLKPDVGVGAANTFKVASDAEVDAALSHPLPTTYVAQPFVRGTIVTYDGIVDRHGVIVFNLSHEYSDGGMETVVEQRDISFWSHKEIPPALDVLGRQVVAAFGLRERWFHLEFFRLPDGRFMVLEANLRPPGGFMVDMMNYTCDIDVYRLWARVVTGDPVADFRFTPRYHVCHSARRKSRRYRHPHADVEKKLGTSLILHRELPSIYHSLLGEEMYLTRHADMDALRDTVRFIQDKA
>NZ_CP017169.1|WP_140787017.1|656735_657308_-|TIGR02265-family-protein
MKHRRAVPLEQRLVYVQVVEGLLEHGLRGSVSPRLKHRLRQAGIDLDRPLLPGYPVLLWGKCLDVIVEEAFPGLPREEAFRQLAERHVQGYGRTVLGRAVYGVMRLLGPRRLVQRLPQTLRATDNYTEVELTEQGPTTYAMRMNSRVDAPGYAEALFESLLRLGGAESPRVARIHEDADSTTYQLTWAAR
>NZ_CP017169.1|WP_140787019.1|657318_658092_-|alpha/beta-hydrolase
MGHVHIVRDFPSPQEGFARTVRVYTPHAYDAMPGHRFPVLYMHDGQNVFAHPESALFETWCANLALEHGVGEGSLEPWLIVAVDSGVGRVHDYSPWNEPRSPMHARGEAYGRFLVEHLKPLVDRTYRTRTEPQWTGAMGSSLGGLISLYLGCRYPEVFGRIGALSPTVTWGANQLFGAWSAHSRRWTRIYLDAGAHEYTDASGVPVYYGESTRAFYEHLKHLGYADHELALVLDPHGGHHERDWQRRLPSAMRWLLG
>NZ_CP017169.1|WP_140787021.1|658224_658416_+|hypothetical-protein
MELEHPHLAVLLLTTESDLREAREALDGSEESRLRYVAAESRAEAAYFLAWDLLEVDPRMGRA
>NZ_CP017169.1|WP_140852955.1|658498_660622_+|hypothetical-protein
MVLDVHKARCVRRVLWVGWCLGWWLAGALPVHAAPYEVEPESVGAQDLLALVEEGAISAETLSTLLALRRTGVDLGLASRASLYGLPGLTYSDVDVLLRSRGEGGAAGGALTEAASRRLAPFLEVRTPGRLSGDARLMMAFAASDGLPPPLALQVRAGGLAGLRVGLLTTLARRTLEPPRRDARRRAFVVEAPGTSVMLPKLYVQWTGARASLLAGTYRLGFGQRLTLDTTALPSPDGFLPDDNVRPPAGLERACLAGGAGCEPEERLSDVTPDFRWDEGFRGVAGTVRGPLGTGAALSLTGFGSYQSRALARHAVLDRSLCPSSARGVCKAPDVWVSVAEGRWEKLTARTLPGMFRELAGGGNATLALSSRSHVGLTGWMARPVWGQEGAKLDFQPNARYPAGGAFGAFGLDAAWGRGALDVFFEGTRSFDAAPGGGGDFGAVQRTVLSGESRELELSLRYYGRGFANPYSGATSGPDALEGLRVRNELGARLRYLHREEGAWRLRGQVDAWTLPADGEVSGSAGTLHARASMRGDLRVRPWLQPSLQVELRDNGVGGMGACADDSLSAQEVADLCASARYGVTARVRSDVAKGLTVSLQYGHARVQAPETKGLRDDAQAVLDVRAQPLASLKLHGRLVWKDQDLSERSRLQQELRTALDVAWRVSSAVSARGRYAWVLDLKDARVARVPPDPPRHLFHLELETRF
>NZ_CP017169.1|WP_140858155.1|660648_662460_+|lamin-tail-domain-containing-protein
MKGWGRYLGWGWLLGLAGAWACGGTSLDEDVDAACAGLLPGDVVITEYLNDPVGSDTGQEYVELHNPTRIPVDLYGLTLYASRSDGSQEKAYAVLDEMTVAAGDYLVLGDVRDGPVPAHVDHAYGDGLGALGNSGGRLGIRCGERVLDEVQLSAPAKSGASRIYDGRLVPDMAGNDDQARWCDSPDAGVGGTLQGSPGAANAPCGPVGDAGVPADAGVVATCRPAGADAGRPVLLPAPGDLVITELMANPRGDDTLGEWVELRATAPVDLNGVTLVAEAGEATVKADGCLSLATGEYAVLARRTDATLNGGLPPPVATFNMDLRNAGGRLQVKAGGVVVDAVDYGLAMDGVATQVSAPLADAVQNDAPSAWCAATAAYGSRGDLGTPGRGNRVCEGDGGTLGGAGDGGTSDGGVDAGTLEDGCIDRTTGRTRARRVPDGGSLVLTEFMADPQAVADAMGEWVEVLALRDVDLNGVSLSNESGSRSTFDSALCLAVKAGGRAVLARSEDASRNGGLPAVLGTFNFNLANTTGSRKLELSVEGRVLDAVSWTGAAIPGVSSQLDPGRSDPQRNDWPGSFCPTPESARYGRGDRGTPGGVNRSCAP
>NZ_CP017169.1|WP_140800596.1|662459_662933_+|thermonuclease-family-protein
MKCALACLLAACGGGDAEVSCGPASGRVAEVLDGDTVVLESGERVRYLLADAPERTGAGGDCFGPEAHAFNRGLVEGRRVALTYGEACEDRFGRRLAYVSVDGREVNTLLVERGHACVLHVPPAGRSRRAEFEALEAQARLARRGVWGACAPVPCQR
>NZ_CP017169.1|WP_140787025.1|663139_665404_+|PAS-domain-containing-protein
MSPSVTPTLSLPDVLEVLREDIIRRLMAGVGAALGALAPLASADAGGLHKLVGRLGALLRIPSMAARLAEARALGREYGRERYLAGFSISSLVLEYGALREAILESLEAVGWVPELAGLRALAQVLDAGLAEAVGQSSLEDERTARATGAWLHGLLDHAPTLIYAKDTAGRYLYVNHGFERASGKLRRDVMGRTDFDLFSAEVASTFSGNDRQVLDSGQQLTIDEHVPLIDGLHVFQTLKFPLPDAQGRVVGVCGFSTDFTEAKRLERERDEAREHLRRIVTQLPVILWATDAQGIITLFEGERLSALGLERGAYVGRSAFDVYRDRPDLVAATMRAQEGQSFTLEVEMAGSYFMTGVSPVIGPDGSVMSVAGVSLDISERRRAEEVLRQSEMRYRLATLATSDVIYDWDLDAGTVEWSELAAAQFRLASRAPPRDIAWWTEHIHPEDRERIARDMQAVIDQGASHWADEYRFLRGDGTWAVVADRGQVVRDAEGHAVRMVGAMQDITERRATELEAKRRAEFEQLLIGIVSHDLRNPLAAISMSATALLRREGQDERLRKGLGRILSSAERATRMLRDLLDFTQARLGGGIPMEPQWLDLHELTRQVVEEVRLTRPERTLELECRGDGYGLWDADRLAQVITNLVNNALSYSPEHCPVRIRTHGLRDDVLLTVHNAGGPIEPELRTRLFEPMKRPERKGARGGLGLGLFIVKHIVDAHGGAVRVHSTEQEGTTFQARLPRQPMPPARPDVDAP
>NZ_CP017169.1|WP_140787027.1|665481_666312_+|hypothetical-protein
MKKVLIGLGIGCGVFILAGIGLMLAGGIWAKNKFGGSIEAMQAMQAQEQELTQLNASNPFKAPPEGQVLPLDEQRLLAYLTVRESALPAFKAFEVKSKEFEAQHEGDGDEKPGFNAAVDAAGLFMGLMADVRKAYIAGLKAQGMSPAEFQSITTTVYASMVADSLDQIGAAAEQGRKMMVTQLAEVDKRLADDSLADEERAQLEEARAQLQETLDTIEETHANEEQPLSEESKKAAAANVALLKKHKERVELMANVAFDGFVLGGAGADGQAAGLE
>NZ_CP017169.1|WP_162521002.1|666342_666681_-|hypothetical-protein
MSSGPWCWCCSRWTPCPLYNSNAFAILGLRALYLVLAGTVGTLRYLHYDLAGVLAFAGLKMVLEPWLHAPPMTSVLIIVTLITGAVWASQRARRREARAAASRPGAPVEREA

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Crispr_ID: NZ_CP017169_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_3

1058120-1058218

Orphan

Consensus_repeat	Method
GAGTCACCGACACGGACTCCGTGCCCGTCGCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_3

>merge|NZ_CP017169|3|1058120-1058218|CRISPRCasFinder
GAGTCACCGACACGGACTCCGTGCCCGTCGCCGACGCGCCGTGTCCACTTGTCGCCAGGGCTTCCGGAGTCACTGACACGGACTCCGTGCCCGTCGCCG

>NZ_CP017169|3|3|1058120-1058218|CRISPRCasFinder
GAGTCACCGACACGGACTCCGTGCCCGTCGCCG	ACGCGCCGTGTCCACTTGTCGCCAGGGCTTCCG
GAGTCACTGACACGGACTCCGTGCCCGTCGCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140787601.1\|1044208_1044649_-\|host-attachment-protein	unknown	unknown	gnl\|CDD\|370820
NZ_CP017169.1\|WP_140787642.1\|1064278_1065364_-\|esterase-family-protein	unknown	unknown	gnl\|CDD\|225256
NZ_CP017169.1\|WP_140787640.1\|1063537_1064137_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140787644.1\|1065373_1066279_-\|TIGR01777-family-protein	unknown	unknown	gnl\|CDD\|187553
NZ_CP017169.1\|WP_140787652.1\|1069596_1070607_+\|squalene/phytoene-synthase-family-protein	unknown	unknown	gnl\|CDD\|173831
NZ_CP017169.1\|WP_140853088.1\|1049255_1050680_+\|hydrolase	unknown	unknown	gnl\|CDD\|366286
NZ_CP017169.1\|WP_140853086.1\|1046976_1048491_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017169.1\|WP_140853083.1\|1042215_1044111_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223910
NZ_CP017169.1\|WP_140853084.1\|1044844_1046053_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140853085.1\|1046058_1046850_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368175
NZ_CP017169.1\|WP_140853091.1\|1056494_1057157_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP017169.1\|WP_140853095.1\|1070667_1072125_+\|phytoene-desaturase	unknown	unknown	gnl\|CDD\|274273
NZ_CP017169.1\|WP_140853087.1\|1048534_1049071_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238017
NZ_CP017169.1\|WP_140853094.1\|1068046_1069600_+\|phytoene-desaturase	unknown	unknown	gnl\|CDD\|274273
NZ_CP017169.1\|WP_140787648.1\|1066953_1068039_+\|polyprenyl-synthetase-family-protein	unknown	unknown	gnl\|CDD\|173833
NZ_CP017169.1\|WP_140853090.1\|1051833_1056336_+\|lamin-tail-domain-containing-protein	unknown	unknown	gnl\|CDD\|275366
NZ_CP017169.1\|WP_174258647.1\|1066275_1066839_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239264
NZ_CP017169.1\|WP_174258646.1\|1050687_1051539_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140853093.1\|1058932_1063333_+\|chromosome-condensation-regulator-RCC1	unknown	unknown	gnl\|CDD\|227511
NZ_CP017169.1\|WP_140853096.1\|1072121_1073051_+\|carotenoid-1,2-hydratase	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140787601.1\|1044208_1044649_-\|host-attachment-protein	gnl\|CDD\|370820	pfam10116, Host_attach, Protein required for attachment to host cells. Members of this family of bacterial proteins are required for the attachment of the bacterium to host cells.	1.82776e-36
NZ_CP017169.1\|WP_140787642.1\|1064278_1065364_-\|esterase-family-protein	gnl\|CDD\|225256	COG2382, Fes, Enterochelin esterase and related enzymes [Inorganic ion transport and metabolism].	2.31208e-31
NZ_CP017169.1\|WP_140787652.1\|1069596_1070607_+\|squalene/phytoene-synthase-family-protein	gnl\|CDD\|173831	cd00683, Trans_IPPS_HH, Trans-Isoprenyl Diphosphate Synthases, head-to-head. These trans-Isoprenyl Diphosphate Synthases (Trans_IPPS) catalyze a head-to-head (HH) (1'-1) condensation reaction. This CD includes squalene and phytoene synthases which catalyze the 1'-1 condensation of two 15-carbon (farnesyl) and 20-carbon (geranylgeranyl) isoprenyl diphosphates, respectively. The catalytic site consists of a large central cavity formed by mostly antiparallel alpha helices with two aspartate-rich regions (DXXXD) located on opposite walls. These residues mediate binding of prenyl phosphates. A two-step reaction has been proposed for squalene synthase (farnesyl-diphosphate farnesyltransferase) in which, two molecules of FPP react to form a stable cyclopropylcarbinyl diphosphate intermediate, and then the intermediate undergoes heterolysis, isomerization, and reduction with NADPH to form squalene, a precursor of cholestrol. The carotenoid biosynthesis enzyme, phytoene synthase (CrtB), catalyzes the condensation reaction of two molecules of geranylgeranyl diphosphate to produce phytoene, a precursor of beta-carotene. These enzymes produce the triterpene and tetraterpene precursors for many diverse sterol and carotenoid end products and are widely distributed among eukareya, bacteria, and archaea.	9.5079e-89
NZ_CP017169.1\|WP_140787644.1\|1065373_1066279_-\|TIGR01777-family-protein	gnl\|CDD\|187553	cd05242, SDR_a8, atypical (a) SDRs, subgroup 8. This subgroup contains atypical SDRs of unknown function. Proteins in this subgroup have a glycine-rich NAD(P)-binding motif consensus that resembles that of the extended SDRs, (GXXGXXG or GGXGXXG), but lacks the characteristic active site residues of the SDRs. A Cys often replaces the usual Lys of the YXXXK active site motif, while the upstream Ser is generally present and Arg replaces the usual Asn. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	4.90167e-119
NZ_CP017169.1\|WP_140853088.1\|1049255_1050680_+\|hydrolase	gnl\|CDD\|366286	pfam00756, Esterase, Putative esterase. This family contains Esterase D. However it is not clear if all members of the family have the same function. This family is related to the pfam00135 family.	1.35653e-20
NZ_CP017169.1\|WP_140853086.1\|1046976_1048491_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	5.11782e-101
NZ_CP017169.1\|WP_140853083.1\|1042215_1044111_-\|HAMP-domain-containing-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	7.83651e-51
NZ_CP017169.1\|WP_140853085.1\|1046058_1046850_+\|hypothetical-protein	gnl\|CDD\|368175	pfam04885, Stig1, Stigma-specific protein, Stig1. This family represents the Stig1 cysteine rich plant protein. The STIG1 gene is developmentally regulated and expressed specifically in the stigmatic secretory zone.	0.00440955
NZ_CP017169.1\|WP_140853091.1\|1056494_1057157_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	3.1794e-14
NZ_CP017169.1\|WP_140853095.1\|1070667_1072125_+\|phytoene-desaturase	gnl\|CDD\|274273	TIGR02734, Phytoene_desaturase_lycopene-forming, phytoene desaturase. Phytoene is converted to lycopene by desaturation at four (two symmetrical pairs of) sites. This is achieved by two enzymes (crtP and crtQ) in cyanobacteria (Gloeobacter being an exception) and plants, but by a single enzyme in most other bacteria and in fungi. This single enzyme is called the bacterial-type phytoene desaturase, or CrtI. Most members of this family, part of the larger pfam01593, which also contains amino oxidases, are CrtI itself; it is likely that all members act on either phytoene or on related compounds such as dehydrosqualene, for carotenoid biosynthesis. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	2.03506e-79
NZ_CP017169.1\|WP_140853087.1\|1048534_1049071_-\|FHA-domain-containing-protein	gnl\|CDD\|238017	cd00060, FHA, Forkhead associated domain (FHA); found in eukaryotic and prokaryotic proteins. Putative nuclear signalling domain. FHA domains may bind phosphothreonine, phosphoserine and sometimes phosphotyrosine. In eukaryotes, many FHA domain-containing proteins localize to the nucleus, where they participate in establishing or maintaining cell cycle checkpoints, DNA repair, or transcriptional regulation. Members of the FHA family include: Dun1, Rad53, Cds1, Mek1, KAPP(kinase-associated protein phosphatase),and Ki-67 (a human nuclear protein related to cell proliferation).	2.81373e-05
NZ_CP017169.1\|WP_140853094.1\|1068046_1069600_+\|phytoene-desaturase	gnl\|CDD\|274273	TIGR02734, Phytoene_desaturase_lycopene-forming, phytoene desaturase. Phytoene is converted to lycopene by desaturation at four (two symmetrical pairs of) sites. This is achieved by two enzymes (crtP and crtQ) in cyanobacteria (Gloeobacter being an exception) and plants, but by a single enzyme in most other bacteria and in fungi. This single enzyme is called the bacterial-type phytoene desaturase, or CrtI. Most members of this family, part of the larger pfam01593, which also contains amino oxidases, are CrtI itself; it is likely that all members act on either phytoene or on related compounds such as dehydrosqualene, for carotenoid biosynthesis. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	6.98273e-165
NZ_CP017169.1\|WP_140787648.1\|1066953_1068039_+\|polyprenyl-synthetase-family-protein	gnl\|CDD\|173833	cd00685, Trans_IPPS_HT, Trans-Isoprenyl Diphosphate Synthases, head-to-tail. These trans-Isoprenyl Diphosphate Synthases (Trans_IPPS) catalyze head-to-tail (HT) (1'-4) condensation reactions. This CD includes all-trans (E)-isoprenyl diphosphate synthases which synthesize various chain length (C10, C15, C20, C25, C30, C35, C40, C45, and C50) linear isoprenyl diphosphates from precursors, isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). They catalyze the successive 1'-4 condensation of the 5-carbon IPP to allylic substrates geranyl-, farnesyl-, or geranylgeranyl-diphosphate. Isoprenoid chain elongation reactions proceed via electrophilic alkylations in which a new carbon-carbon single bond is generated through interaction between a highly reactive electron-deficient allylic carbocation and an electron-rich carbon-carbon double bond. The catalytic site consists of a large central cavity formed by mostly antiparallel alpha helices with two aspartate-rich regions (DDXX(XX)D) located on opposite walls. These residues mediate binding of prenyl phosphates via bridging Mg2+ ions, inducing proposed conformational changes that close the active site to solvent, protecting and stabilizing reactive carbocation intermediates. Farnesyl diphosphate synthases produce the precursors of steroids, cholesterol, sesquiterpenes, farnsylated proteins, heme, and vitamin K12; and geranylgeranyl diphosphate and longer chain synthases produce the precursors of carotenoids, retinoids, diterpenes, geranylgeranylated chlorophylls, ubiquinone, and archaeal ether linked lipids. Isoprenyl diphosphate synthases are widely distributed among archaea, bacteria, and eukareya.	7.24162e-62
NZ_CP017169.1\|WP_140853090.1\|1051833_1056336_+\|lamin-tail-domain-containing-protein	gnl\|CDD\|275366	sd00002, TSP3, Calcium-binding Thrombospondin type 3 (TSP3) repeat. TSP3 repeats of the vertebrate thrombospondin (TSP)-1,-2,-3,-4 and TSP-5/also known as COMP (cartilage oligomeric matrix protein), and related proteins. These short aspartate-rich repeats are a continuous series of calcium binding sites that can be divided into two sequence motifs: N-type and C-type. N-type and C-type motifs are distinguished by their sequence length, calcium ion binding, and their interactions with water molecules. C-type motifs are higher affinity binding sites compared to N-type motifs.	3.88791e-24
NZ_CP017169.1\|WP_174258647.1\|1066275_1066839_-\|hypothetical-protein	gnl\|CDD\|239264	cd02966, TlpA_like_family, TlpA-like family; composed of TlpA, ResA, DsbE and similar proteins. TlpA, ResA and DsbE are bacterial protein disulfide reductases with important roles in cytochrome maturation. They are membrane-anchored proteins with a soluble TRX domain containing a CXXC motif located in the periplasm. The TRX domains of this family contain an insert, approximately 25 residues in length, which correspond to an extra alpha helix and a beta strand when compared with TRX. TlpA catalyzes an essential reaction in the biogenesis of cytochrome aa3, while ResA and DsbE are essential proteins in cytochrome c maturation. Also included in this family are proteins containing a TlpA-like TRX domain with domain architectures similar to E. coli DipZ protein, and the N-terminal TRX domain of PilB protein from Neisseria which acts as a disulfide reductase that can recylce methionine sulfoxide reductases.	6.8111e-05
NZ_CP017169.1\|WP_140853093.1\|1058932_1063333_+\|chromosome-condensation-regulator-RCC1	gnl\|CDD\|227511	COG5184, ATS1, Alpha-tubulin suppressor and related RCC1 domain-containing proteins [Cell division and chromosome partitioning / Cytoskeleton].	1.10535e-52

>NZ_CP017169.1|WP_140853091.1|1056494_1057157_-|TetR-family-transcriptional-regulator
MAREPAQRELKQERAARTRMDILEAAIHLFARRGFLATTMADLSRAIRMTPGALYWHFPTKEDLLLAAIEELHQRCLRAFQLPGDDRELPAREQFQAICERTHLLLREHREYGIFFAMLAAEAADSNAQVAEAIRDKLALYATTLERLIRHGQQMGEFRQDVDALAAAHSLLGGLLGMLVHQNLFRASVDYDPLYRAVMLIHQAGLVQATGFDCVNASQS
>NZ_CP017169.1|WP_140853090.1|1051833_1056336_+|lamin-tail-domain-containing-protein
MRMSPRLLLAALGAVLLFHAGCGDEPGCEGASCNPQAVCGNNVVEQGEQCDDGNKVDGDGCESNCTPTPAPGAVCGNGKLEGEEVCDDGNTVDGDGCQANCTPTLTQCPAANAPALPDGATCAVTQPGSAARLFTGVVLKDGETLVGGQVLVDAQGVIQCAACDCSAAAGAAEATQVSCPGGVISPGLVNPHEHITYPMEPYVGSEERYEHRHEWRTGRNGHTRINSPAASAADNVRWGELRQMMAGATSMAGAGGQAGLLRNVDVNNTALQEGLGEGVVNSDTFPLGDTSGNLIASGCGYGSMPTTSSLPRSAAYLPHISEGISTAALNEFLCLSTGQNNVMQPRTAVIHGIGLTAKEIRVMAENGTGLIWSPRSNISLYGDTAMVTAYKNQGVTIALGTDWLRSGSMNLLRELQCADYLNTSHYARTFSDEDLWRMVTSNASDLVDTFEKTGRIAEGKVADLAIFQLRTFAHSPHRAVVTANPEHVVLTMRGGKALYGDQALMAGLRGADTCDTLDVCGASKEVCLQSEIGKNLAALTSGATAKYPLFACGTPENEPTCSPRRASLDSRWPAVVNNSTSYTGEVRAADKDGDGLVDSVDNCPAIFNPIRPMDNGKQADSDGDGIGDACDPCPLEAGNACTSFTVGDDDHDGIVTWLDNCPFVANPDQADADGDGKGDACDACSSVPNPGDLGCPATIHELKTPVGGSLPLVGKPVSIMDVVVTGVVKGGASSQGYWVQTYPLPSGTSVDNSGLYVFSPKGDLAVGDRIDITTGVLLLYFGLPELTEVKYVKRSSGNEVPAPVVVTTADIRTGGPRAAALEGVLVEVRDVAVNTGVDEFGQFLVNEAGDAGQPGLMIDDQAYAFPVPSIGTRFGALRGVLTYNFNDSKLVPRFQADMPLPPPSLTGFGPNGYARVGGTGPVNTFPQALTLTLSSAYAEALDVVITSSDESALSVQGGRITIPAGQTSATVQVNAVAPAQSVTLTATLGGSTQMATVRVLGADEQPEVVGVTPGDVTMVPGGEVVFTVRLDRPAPANATVALSVNPATGFGTFVPANGTLTVTENATEAVFSFITEAAATATEPGTVTASIGASSASATVTLDQNAPRLTALSPSSAVTIPAGGTQTFTLTVDRPAAQDTVVELAVVPGAGVQNYGTVPASATIPAGATEVTFTFTADAQGEGTGTVYATLYGITQTTELTVLPPPPALSAVTPAVATVYFGTQQVFTVALDRRAPAGGITVDVALEPATGMGELSSSTVSIAEGQTTGTVTFTAGEEDAQGRLIASYAGVTRGVDITIAERPAVGHIVISEISARGATAQNDEFIELYNPTGADITLNGWKVQYKSAASTTNYSGSVDIPDGTVIKAYGYLLLAHNSGYTGTVTKDVGYAFDMSASTSGGGHVRIGPNLAADNLNDPNTVDKVGYGTANQPEGSAAPAHPGAGGSLERKARPNSTAETMAVGGADALAGNGHDTDDNGSDFIVRAASQPQNSQSPAERP
>NZ_CP017169.1|WP_174258646.1|1050687_1051539_-|hypothetical-protein
MDVAVLTFEGLPQLDAFDASLLPALAALGVEARPVVWDDPAMDWKTVRLALVRNTWDSHLRRDAFVAWADKVGRLTQLHNPAPVLRWNTHKHYLRELEEKGVLVTPTTWVRKGDTLDVGELAIRHGWDAVVLKPAVSAGALKTHIFPRAEAHAATARLAEMTRDGDVMVQPYLTAFETEGERSYVFFDGVLSHAVRRPPTLLDAPRGFSEPTAFTPEDAAELRLAESVLEAVGRPLLYARVDVATDNAGQARLQELEATEPRLFLSLDAGAADRLAGAIVAKL
>NZ_CP017169.1|WP_140853088.1|1049255_1050680_+|hydrolase
MRRLLAAVFCAAAVLAACEDDSPPPPTPPPPSTETYPDAGTRPDAGPQEPWACQRSTTVHNAPMRLLTRLQLEMSRATSSAQRTEAIDRFVAEVEEQGGRPLVSDVKAGRPRVAFFVRGEAGRDTFVAGDFNGWSATATPLVQVRDTDLYVAEVEVPRTGPQPYKLVKDGDFIADPGARHVAWDNFNRYDVGQFNSLIYPELQDAAKGRLTAWYGVPATVLGDVRDVFVYTPAAYDGRECPALPVMYLHDGNESLTRESFAEAADTHYAARPEDSAVLVFVALPDQSVRLAQYTFPPARAPGWPTPRGDDYLAFIRDDLMPRVEASYRVKTGPRETGIAGASLGGLISVYAGFQMPEKFGFVGSQSGTLFWPHDGEVDRDDGNAMILRAGQEPVVPVRFYVDHGSPVAGCTRDGEEGGDDCQSNLQFVEALRGRGYGVAHWNEPGAEHDWAFWKRRLPKLLCNFRNAAPAVCGL
>NZ_CP017169.1|WP_140853087.1|1048534_1049071_-|FHA-domain-containing-protein
MARALLLSLLVRQHMALKEKFRAKYPHPWLVWEAGAWNVPEVVEGNVAATRLPLTDLRDCLPAGDALCFELVGHTDGSPLRLGRASNNALVVNDATVSREQLHLSPTLEGRWTVTRVAASRPVTLGGTALEPEQPTVLQPGAQLHVGDVRLTFHEAEDFNERIGRIAAQVLAQTAAPR
>NZ_CP017169.1|WP_140853086.1|1046976_1048491_+|protein-kinase
MGSDDAFMQTVQSRAEATVSDAGARASDELQEGSTLGNYQLEQFLGEGSMGRVFQARHTRLGRQVALKVLRPEHARDGGFVRRFFQEARTVNQINHEHIVEIFDFVDESATGGHVYCVMELLRGQSLSSLAQAEPLTLARIQRFVVQVCAALGAAHQVGVVHRDVKPDNLFVIHRAGQPDFVKVLDFGVAKLLTAEGGTTGTVDGTIIGTPAYMAPEQAAGLPVDARSDIYAVGNILYELISGKPPFQAPAFGHLVVQIITQPPPPLPSHLPSGEPVPPQLAELVMRCLSKEPEARPQSLAEVTTALLLLPASAQALTLAPAELALEASERPTHKVRVAVTGRWHRRAVVTVGTAALVVVAAVVTWSGMQPEPAPAAAPVAHAADVVARSVAEAPAAPAAALQLLPPVTLTVRSFPEGAQVLRLDTGELLGVTPLVKQVSGEPAPLRLRVELAGYAPLERMVNLDKHAELEVPLVKALPSPRQKPAAGTQRATDKKSRARPVTQ
>NZ_CP017169.1|WP_140853085.1|1046058_1046850_+|hypothetical-protein
MKTFESRLRVWCGLLLVAGAVGCTVNFPDDVPYTCTETADCGGDGYVCTSLPDNGPRYCCLPDPAEVCNGLDDDCDGLVDNLETACYTGPEGTLDVGLCHAGESICTRDASIACVGEVLPGLETCNGLDDDCDGAVDEDFDLKTDPGHCGACNNDCSFLQDCVNGECVRRQELDCANGQDDDGDGFTDCQDRADCDGQSCGSQCVCQGGSKTETSCTNGEDDDGDGLVDCADRADCPTNTQCGPLRSADENDYPRCQVNGVCL
>NZ_CP017169.1|WP_140853084.1|1044844_1046053_+|hypothetical-protein
MRIPVAPVTALLALALLAAPSWAQEQGGLGLDLTSDAPAEQQGMDIGLDLRPSNPNADLLPRFALVGLYATERAGAQQASSWVEALARGALSSAMVAQASDLVETRERLAEGYDAAVRCAEAACFAEPAELLDADLLTTARLSLEDAGWTLRTWTYDRDRRVVHEDFVTGRNPRDEDFVNEAAAMLSKRLTALARPRAMLTVNVNVPQAVVKVGERIVGVGSVEVRQAPGPVVLEVSADEYGTHARTLDLKPGARETVDVMLEISGPAPDGPPDDSVAGVASSRKVPRKSLFKRPALYTALLGLAAVGAGVVMGMAAKDVEKRGGDADGDGMFDVTRKERLDAQSQANLATALLVGGGAVTAGSVAWLVVVPARSAPASTSVASGSSGGASTSLHLMVGGSF
>NZ_CP017169.1|WP_140787601.1|1044208_1044649_-|host-attachment-protein
MANGTLWILVGNASRARLFATDAKAEEDWRLVEEFHHDESRARQAELIEQADNPNAGTLHGPPAENEPNGRRELEHDRFARELSVFLDKAHDRHDFDKLVIAAPPGFLGRIRRSLSARVRQRVLLDVDSDYSNVPAKELPNRVPVI
>NZ_CP017169.1|WP_140853083.1|1042215_1044111_-|HAMP-domain-containing-protein
MALSLPGTQSLRGRLTLYATLLSVVPLLTLTWLQARSARQVMEEQIHASLLSEAEGVKDLLESTLAEREASARGWAEDPAVRAALRGDVSPADAMLGVLQSRYLTLNGIVVFDDTGRAISANTPALRDEYLRRQDEVRRSPWFAEAQQGRTSSEGITEEHPIFTGHVLSLAFPVLDPVSKHRMGVLLAAFDWAHVDQLVQPALARAHQRALKSFSITLQRPDGTPMYDSRGANAQGNDALLAVTAVNGTDVRDVADGWHFVARVDPAEAYAPVVRVSRVALLMAVGFIVLAVVGAWLLSHRISGPVLALRAAVTRLVSEGDLTQTLDVKAGNDEVGELAGAFGLLVFQLRETAQSLHTGTRVLSETVAELQTASTQQERNVARQAAALQQTQVTAQEIKQTSMLASEKAEDVLKRASMAEEVGRAGEGAIRDSLGGFSEILSQAEQMTERIAQLNERTQQIGGITQTVKDLADQSNMLALNAAIESVRSGEHGKGFGVVAREIRSLADQSIQATDRVREILGDLSSAILSTAKMTEQGYTHMESGLEQVRGTGERLKELAAIIQDNATAVRQIAGAVSQQNAGIAQIFSAVTDLSSMMNDTQESLAATTRAAKLLQDVSEQMQDVARAYRI
>NZ_CP017169.1|WP_140853093.1|1058932_1063333_+|chromosome-condensation-regulator-RCC1
MHHLIEETPMPPDMMAGTRRLLMCLLSALLMAGCEPSGELAMPETPHATRTQRVVVTAPPMRIAAGSQHSLYLSPGGDVWAWGGNGSGQLGGAETSLLGLAPVRLAALEDIVSVVSGEAHSLALGADGTVWTWGGNSSGQLGDGSTTDRATPMRVAGLDNVVAVAAGDFHSLALREDGTVWAWGTNFHGQLGRGHTQPGLTPERVPGLNGVVALAAGFDFTLAVLEDGTVRAWGSNGSGQLGDGTFTQRLSPVKVSQLSGITAVTAGTYHALALGKDGGVWAWGSNASGQLGDGTWNDRAVPMQVPGLERVKAVASMDSDSLALLEAGAVFAWGANGSGQLGDGDTTDRATPGPVPGLNAVASVVGGAQHALALRKDGTLWAWGGGLSGQLGHGGSERHVVPAPVMRLAGVTSMATGSFHSLAALGDGSVWAWGRNTSGQLGDGSTAERHAAVRVEGLGGVRSVASAAHHSLAVGMDGTVWAWGRNAAGQLGDGTTTDRARPVAVPGLTSVTAVAAGGSHVLALRSDGSVWAWGYNALGQLGDGTTVDRLTPVRVSGLGAVVAVAAGSYFSMALQSDGTVWTWGEGFEGQLGDGGGVQRLSPVRVEGLANVTRVAAGSAHALAVRGDGTVWAWGDNGEGQLGDGSWADRFRPVQVPGLQGITAVSGGRSHSMALQGDGTVRAWGYNGYGQLGDGTLTSRVRPALIPGLTGIQALHPSHLHVLALHADGTLRGWGYNRFGQLGLGAAGWSALPVQVRGIGRVDRLSVGRAHTLMVRADGTVMAWGENGSGQLGDGTSTHRAGPVSVRGVPCVRSVASGLRHSLALACDGTVWAWGANGRGQLGDGTTTPRVTPGLVEGLRGVVALAAGGDASVALRADGSVWSWGGNASGQLGDGTTTDRALPAHLEHLSNVVAVAVGETHALAVGEDGALWAWGANGSGQLGDGGTEPSLTPVRVKGLERVASVAAGRAFSVAVRDDGTAWAWGANPSGQLGDGTNLARSVPKQVASVKGIRAMSAGAHHVVALSADGTVWTWGDNTLGQLGDGSSSPTWMYPRQVPELRGVEAVAAGEQFTVAVLLDGTARAWGSNEYGQLGDGKTGPQLTPMAVKIDGPKIRPPVRAVRAWGQHAVVQMSDGTVQAWGDNAFGQLGDGTTTRRAVPLEVRGLASVVAVSSGAWHSLALRSDGTVWAWGANGFGQLGDGTSTSRTRPVQVAGLGDVVAIGSGGYHALAVRSDGSVWTWGYNAFGQLGDGTAESRSLPIRVEGLEGVVAVAGGDHYSLALHSDGTLSAWGNNASGQLGDGTGTTRYSRVGVKGVDGVVDVRAGAAHTVALRGDGTVWTWGDNAFGQLGDGTSGTRMRLVPQPVPSLSSVSAVGAGARHAFAVGLKGAVWTWGRNSHGQLGLGDNANRTEPLRVRELTDVTVVSGGADFSLAMKRDGTVLSWGSSLYGTLGLGAAGQRSSPGQVALP
>NZ_CP017169.1|WP_140787640.1|1063537_1064137_-|hypothetical-protein
MSRIDGGNRPSSPKGPVHERASAPEQRPASGTATQGTKGVQAHRTVQTFQGRSDFEPDRRPAQRGVTAPPPPPDATAIAGADAELELLSEFPDQADAQGGLASAMLHAHANEPASQARIVERLKQDGRLESLFGEVFREGNPYVEQPHRNAVVRALGTAMARGTVTSDDLRAFARGAYAQEWRQIGSELTTPRPLTEKP
>NZ_CP017169.1|WP_140787642.1|1064278_1065364_-|esterase-family-protein
MDAKTLEARARAEGTPVIDSDTATFVWRGRGPICLQGDFQDWRGKPLPLKRVAPGLWARTLTLPADAYVEYALEDPRGRRVEDPLNRHPSDNGFGGINHSFHMPQARSSLPARHPRGAPRGRVTRHVVDTGDVDLPGQRRVYLYAPPTDAPVPLVVVYDGEDYLRRVRLPELVDTLMAEGRMRPVALALVCNGGETRSMEYACSEYTVGLLKWKVLPLARQKLSLVDERRSPGAHAVLGASLGGLMALYTGLRMPDVFGRVLSQSGAFAVEGHDFVVFDLARPPPRRPLDVWLDCGRFEGLLEGNRRIVPVLSEAGHQVELREYSGGHNYPAWREDLVHGLERHFPPPPAKRRESLRFSGR
>NZ_CP017169.1|WP_140787644.1|1065373_1066279_-|TIGR01777-family-protein
MKVALTGASGFLGPGLVQGLLERGHQVHILSRNVEHALARLPAGVTGAPFDAGSPLPPEALADAEAVVHLAGEPVAQRWTREGKHRIHDSRVLGTRAVVAAMRGAGTVRRFVSASAIGYYGGTRGADPLTEESPPGDDFLARVCVDWEAEAMQARESGIATAVVRMGVVLHPDGGALHKMLPPFRVGAGGPVGSGEQFVSWVHRDDARDLLLFLLAHPQVEGMVNATAPTPVTNAFFAHTLGHVLGRPSMVRMPAFMLKAALGEMAKVVLEGQRVLPQRAHEAGFVFRYTELEGALRDLLA
>NZ_CP017169.1|WP_174258647.1|1066275_1066839_-|hypothetical-protein
MKAWIAGALSISLAAGSALGAAPATEPVDATLRTSAGKEVQLSKWRGKPVILFYEDKDSTKLNSTLKKELFARGQERGILDAAWVLAVANLQNFDFFPARQIALSFVRDEEKKVGVPILVDMDGALGKAPWKLPVKTSNIVLLDSEGALVYRHSGRMKPDELTTFFAVLSRLVGVDLNAPAPSEPSP
>NZ_CP017169.1|WP_140787648.1|1066953_1068039_+|polyprenyl-synthetase-family-protein
MALTLPDAQPPTGLLPLEQAWLQLVQAEVETSLAELFELPDEAGLDVRWTQALTQARAYALRPAKRLRPALVMAGHCLARGSAVVPSGLWRFAAGLELLHTFLLIHDDVADQAELRRGAASLHRLLAPGRAGEDLAVVVGDHLFARALEAMLGSGLTGVAGVVQYYLGVCRHTAAGQYLDLDLGRAPLAEVTLFQTLRVAHLKTARYGFCAPLVCGAMLGGASSGLVEGLERVGRHVGLAYQLRDDLLGLFGDSNVAGKAADGDFLQGKRTFPVLAAFARATEAERMELEALWSLPVEQKDAAALARARALVESCGGRAACERMVVRASRAARRSLQSLPNPNGVRELLDALIARLAHRAA
>NZ_CP017169.1|WP_140853094.1|1068046_1069600_+|phytoene-desaturase
MSASTQGRRIVVVGAGVGGLAAAARLAHQGFDVQVFEKTQGPGGRCNRLQVDGFTWDLGPTIVLMPEVFEETFRAVGRRIEDYLTLLKCDPNYRVHFRDGSDVTFTSELCAMGRELERVEPGSYARYLAFLAQGRVQYRTSLDHLVGRNYAGLRDYLSPRVLARIFQVRAHRRMYGDVSRFFQDERLRAAMTFQTMYLGVSPYASPAVYGLLPFSELGVGIWFPKGGLYAIPQALERLAREEGVRFHYGAPVEQILTDGGRTRGVRLEGGEVVEADAVLCNADLPYAYEKLLDSKATTLKRKEKLRYTSSGYMLYLGMKRRYPELLHHNVVFGRDYKGSFDDIFERFRVPEDPSFYVNAPTRTDASLAPEGKDALYVLVPVPHQHPDLDWKVEGPRVRAKFFARMAELGFPSLESDIEVERVFTPDDWAGTFNLARGSAFGLSQNFTQIGPFRPSNQDARVKNLFFVGASTQPGTGLPTVLISARLVTERLMTWAHAQGVSLSPRTAAATPLEGVAA
>NZ_CP017169.1|WP_140787652.1|1069596_1070607_+|squalene/phytoene-synthase-family-protein
MSPPADKALVERGYVLAKQVTRHHAKSFFFASYLLFGLRRKAAFALYAFCRRLDDMVDGDDAVSAADALPVRLARARQRVAELYLPMPELASRELGPPADRVKGSAAATPWDAREFAALEHTVRHFRIPEQPFQDLISGMEMDLTKHRYTTWAELDLYCYRVAGVVGLMLTPVLGCSDAAAVEPAADLGRAMQLTNILRDVREDLERGRVYLPAEELAAFGLSEDDLRRGQVDARWRSFMRFQVERSRAYYARAAAGVRYLTGFGSQRMVRLMGAIYGDILRDIEARDYDVFSARAHVTTRRKLALASAAMVRPAAVLPVPQGEVRMPLLPTGTGG
>NZ_CP017169.1|WP_140853095.1|1070667_1072125_+|phytoene-desaturase
MKRTRVAVVGGGIGGLTAAGLLAKEGHEVTLFERGTSLGGKAQAVTVNGITLDTGPTLLTLPHLVRGTFQQLGAEDLLPRFTELEPQCAYRFEDGCDFTAYKDVERMAESAAGVRPGERDGIRGFYTEAAAIWRAAGEPYLEAPFEGMAGFMTRVAKRGVGAVMAGMKMGTLHELAARHFMTDHLRQYVGRFATYTGASPYEASAAFALIPHIEHAYGVHHVRGGIGALVDALGQAVRRLGVRIHLDTRARFERTREGYQVGPQEGMERFDSVVVNADPLERLARAEEPLALSGFVLLLEVEGRIALPHHTVLFGGDYRREFDELFGGQLASDPTVYFCNPSATDESMVPPGRTGLFVMVNAPALPVDARGAEQATRDWEAGAERVKAQMLERLCRHYPALKGRVRVIGQRSPVDLAAQGAPGGSIYGFLPHGKFGPFRRPRIRGNTPGLFFAGGGTHPGGGVPLVMLSGRFAAELASQHLRRDA
>NZ_CP017169.1|WP_140853096.1|1072121_1073051_+|carotenoid-1,2-hydratase
MMRLAKLPALPDAAGTYRWFYADVTAGPYSAVCIFMLGSLFSPRYSVAARRGGRPLEHSAVNFALYHEGVRRLWVLSEYARAELETPGRLRIGRSTLSYEGDGTVVRMSVDDWTAPWGRPVRAGLTLEPMTPVGEVVQLMPGLPHYWQALAPRSQARLEVSSLGIEASGLGYHDTNHGGELLGARLSGWHWARTHREDETVVDYHLPEGVAPLRVVAGARGVRCERGPALVEARPTHITSWGLRVPSRLHAGNVVVGQPKLLESSPFYARLEARQGPLDSLGEVADFRRFHSPFIRWMAHFRTRMGRAA

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Crispr_ID: NZ_CP017169_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_4

1170264-1170361

Orphan

Consensus_repeat	Method
CGGTGGTCATCGCGGTGGCGGTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_4

>merge|NZ_CP017169|4|1170264-1170361|CRISPRCasFinder
CGGTGGTCATCGCGGTGGCGGTGGTGACGGCGGGCGTGTGGGCCATCTGGGGACCCGAGCCTCGGTTGGCGCACGCGGTGGTCAACGCGGTGGCGGTG

>NZ_CP017169|4|4|1170264-1170361|CRISPRCasFinder
CGGTGGTCATCGCGGTGGCGGTG	GTGACGGCGGGCGTGTGGGCCATCTGGGGACCCGAGCCTCGGTTGGCGCACG
CGGTGGTCAACGCGGTGGCGGTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140787793.1\|1178606_1179869_-\|TolC-family-protein	unknown	unknown	gnl\|CDD\|224455
NZ_CP017169.1\|WP_140853130.1\|1166246_1167338_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP017169.1\|WP_140858186.1\|1165173_1166211_-\|methylamine-utilization-protein	unknown	unknown	gnl\|CDD\|188554
NZ_CP017169.1\|WP_140853131.1\|1167437_1168835_-\|chloride-channel-protein	unknown	unknown	gnl\|CDD\|238233
NZ_CP017169.1\|WP_140787797.1\|1180382_1181228_-\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|225567
NZ_CP017169.1\|WP_140787776.1\|1163088_1164009_+\|metallo-mystery-pair-system-four-Cys-motif-protein	unknown	unknown	gnl\|CDD\|188567
NZ_CP017169.1\|WP_140853127.1\|1161331_1161946_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|224511
NZ_CP017169.1\|WP_140853126.1\|1158249_1160745_-\|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I	unknown	unknown	gnl\|CDD\|181856
NZ_CP017169.1\|WP_140797341.1\|1177410_1178610_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP017169.1\|WP_140853124.1\|1156054_1157185_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	unknown	unknown	gnl\|CDD\|181076
NZ_CP017169.1\|WP_140853129.1\|1164021_1165161_+\|di-heme-enzyme	unknown	unknown	gnl\|CDD\|188554
NZ_CP017169.1\|WP_140787786.1\|1172086_1173178_+\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|226985
NZ_CP017169.1\|WP_140853125.1\|1157123_1158224_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|181320
NZ_CP017169.1\|WP_140787784.1\|1171584_1171998_+\|four-helix-bundle-copper-binding-protein	unknown	unknown	gnl\|CDD\|153434
NZ_CP017169.1\|WP_140853133.1\|1181348_1184549_-\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	unknown	unknown	gnl\|CDD\|226220
NZ_CP017169.1\|WP_174259034.1\|1174271_1177394_-\|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|226220
NZ_CP017169.1\|WP_174258651.1\|1184535_1186269_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP017169.1\|WP_140787795.1\|1179978_1180293_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_174258650.1\|1162113_1163037_+\|GIY-YIG-nuclease-family-protein	unknown	unknown	gnl\|CDD\|198398
NZ_CP017169.1\|WP_140787787.1\|1173329_1174211_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140787793.1\|1178606_1179869_-\|TolC-family-protein	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	4.51512e-29
NZ_CP017169.1\|WP_140853130.1\|1166246_1167338_-\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	6.40556e-07
NZ_CP017169.1\|WP_140858186.1\|1165173_1166211_-\|methylamine-utilization-protein	gnl\|CDD\|188554	TIGR04039, MXAN_0977_Heme2, di-heme enzyme, MXAN_0977 family. This model describes a subfamily of di-heme proteins related to the di-heme cytochrome c peroxidase and to MauG (methylamine utilization G), an enzyme that performs a tryptophan tryptophylquinone modification to the methylamine dehydrogenase light chain.	5.81043e-86
NZ_CP017169.1\|WP_140853131.1\|1167437_1168835_-\|chloride-channel-protein	gnl\|CDD\|238233	cd00400, Voltage_gated_ClC, CLC voltage-gated chloride channel. The ClC chloride channels catalyse the selective flow of Cl- ions across cell membranes, thereby regulating electrical excitation in skeletal muscle and the flow of salt and water across epithelial barriers. This domain is found in the halogen ions (Cl-, Br- and I-) transport proteins of the ClC family. The ClC channels are found in all three kingdoms of life and perform a variety of functions including cellular excitability regulation, cell volume regulation, membrane potential stabilization, acidification of intracellular organelles, signal transduction, transepithelial transport in animals, and the extreme acid resistance response in eubacteria. They lack any structural or sequence similarity to other known ion channels and exhibit unique properties of ion permeation and gating. Unlike cation-selective ion channels, which form oligomers containing a single pore along the axis of symmetry, the ClC channels form two-pore homodimers with one pore per subunit without axial symmetry. Although lacking the typical voltage-sensor found in cation channels, all studied ClC channels are gated (opened and closed) by transmembrane voltage. The gating is conferred by the permeating ion itself, acting as the gating charge. In addition, eukaryotic and some prokaryotic ClC channels have two additional C-terminal CBS (cystathionine beta synthase) domains of putative regulatory function.	8.04284e-47
NZ_CP017169.1\|WP_140787797.1\|1180382_1181228_-\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|225567	COG3023, ampD, N-acetyl-anhydromuramyl-L-alanine amidase [Cell envelope biogenesis, outer membrane].	3.46937e-48
NZ_CP017169.1\|WP_140787776.1\|1163088_1164009_+\|metallo-mystery-pair-system-four-Cys-motif-protein	gnl\|CDD\|188567	TIGR04052, hypothetical_protein_MettrDRAFT_3899, AZL_007920/MXAN_0976 family protein. Members of this rare protein family regularly occur next to a member of the MXAN_0977 subfamily (TIGR04039) of the di-heme cytochrome c peroxidase/MauG family (pfam03150). MauG itself (TIGR03791) is a protein modification enzyme responsible for the tryptophan tryptophylquinone (TTQ) modification involved in methylamine dehydrogenase activation. All members of this family have a motif of four spaced invariant Cys residues, while additional homologs outside the scope of this family lack the four Cys residues.	7.68944e-103
NZ_CP017169.1\|WP_140853127.1\|1161331_1161946_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	1.63645e-21
NZ_CP017169.1\|WP_140853126.1\|1158249_1160745_-\|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I	gnl\|CDD\|181856	PRK09436, thrA, bifunctional aspartokinase I/homoserine dehydrogenase I; Provisional.	0
NZ_CP017169.1\|WP_140797341.1\|1177410_1178610_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|379862	pfam16576, HlyD_D23, Barrel-sandwich domain of CusB or HlyD membrane-fusion. HlyD_D23 is the combined domains 2 and 3 of the membrane-fusion proteins CusB and HlyD, which forms a barrel-sandwich. CusB and HlyD proteins are membrane fusion proteins of the CusCFBA copper efflux system in E.coli and related bacteria. The whole molecule hinges between D2 and D3. Efflux systems of this resistance-nodulation-division group - RND - have been developed to excrete poisonous metal ions, and in E.coli the only one that deals with silver and copper is the CusA transporter. The transporter CusA works in conjunction with a periplasmic component that is a membrane fusion protein, eg CusB, and an outer-membrane channel component CusC in a CusABC complex driven by import of protons.	2.47315e-53
NZ_CP017169.1\|WP_140853124.1\|1156054_1157185_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	gnl\|CDD\|181076	PRK07671, PRK07671, bifunctional cystathionine gamma-lyase/homocysteine desulfhydrase.	5.39198e-168
NZ_CP017169.1\|WP_140853129.1\|1164021_1165161_+\|di-heme-enzyme	gnl\|CDD\|188554	TIGR04039, MXAN_0977_Heme2, di-heme enzyme, MXAN_0977 family. This model describes a subfamily of di-heme proteins related to the di-heme cytochrome c peroxidase and to MauG (methylamine utilization G), an enzyme that performs a tryptophan tryptophylquinone modification to the methylamine dehydrogenase light chain.	0
NZ_CP017169.1\|WP_140787786.1\|1172086_1173178_+\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	1.71801e-37
NZ_CP017169.1\|WP_140853125.1\|1157123_1158224_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|181320	PRK08247, PRK08247, methionine biosynthesis PLP-dependent protein.	0
NZ_CP017169.1\|WP_140787784.1\|1171584_1171998_+\|four-helix-bundle-copper-binding-protein	gnl\|CDD\|153434	cd08026, DUF326, Cysteine-rich 4 helical bundle widely conserved in bacteria. This functionally uncharacterized protein forms a 4-helical bundle with a bromodomain-like topology. It is present in major bacterial lineages and contains highly conserved cysteines in a repeated pattern, whose sidechains appear buried. Some family members have been (mis)annotated as putative ferredoxins.	3.18985e-28
NZ_CP017169.1\|WP_140853133.1\|1181348_1184549_-\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP017169.1\|WP_174258651.1\|1184535_1186269_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|379862	pfam16576, HlyD_D23, Barrel-sandwich domain of CusB or HlyD membrane-fusion. HlyD_D23 is the combined domains 2 and 3 of the membrane-fusion proteins CusB and HlyD, which forms a barrel-sandwich. CusB and HlyD proteins are membrane fusion proteins of the CusCFBA copper efflux system in E.coli and related bacteria. The whole molecule hinges between D2 and D3. Efflux systems of this resistance-nodulation-division group - RND - have been developed to excrete poisonous metal ions, and in E.coli the only one that deals with silver and copper is the CusA transporter. The transporter CusA works in conjunction with a periplasmic component that is a membrane fusion protein, eg CusB, and an outer-membrane channel component CusC in a CusABC complex driven by import of protons.	6.19997e-100
NZ_CP017169.1\|WP_174258650.1\|1162113_1163037_+\|GIY-YIG-nuclease-family-protein	gnl\|CDD\|198398	cd10451, GIY-YIG_LuxR_like, GIY-YIG domain of LuxR and ArsR family transcriptional regulators, and uncharacterized hypothetical proteins found in bacteria. The family includes some bacterial LuxR and ArsR family transcriptional regulators. The a C-terminal conserved domain shows sequence similarity to the N-terminal catalytic GIY-YIG domains of intron-encoded homing endonucleases. Besides, they have an N-terminally fused transcriptional regulators module, comprising the winged helix-turn-helix (wHTH) domain and uncharacterized domain DUF2087. At this point, they are distinct from GIY-YIG homing endonucleases, which typically contain a variety of C-terminally fused nuclease-associated modular DNA-binding domains (NUMODs). Moreover, some key residues relevant to catalysis in GIY-YIG endonucleases are mutanted or absent in this family, which suggests that members in this family might lose the catalytic function that GIY-YIG endonucleases possess. This family also includes many uncharacterized hypothetical proteins that consist of a standalone GIY-YIG like domain.	1.12508e-45
NZ_CP017169.1\|WP_174259034.1\|1174271_1177394_-\|efflux-RND-transporter-permease-subunit	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0

>NZ_CP017169.1|WP_140853131.1|1167437_1168835_-|chloride-channel-protein
MAGRREPLDEEQSALHDSWDTVLRTVGRVVLGTVLIWGVCSALRYGVHATSDTLLAFASGRSLWWAPLVLAGVLLLGGLLRGLLNRRPGWSDVASDGVNVALFNYHITYEDPADDPRPRYSRPAIRLALRKAVATLLTLGTGASGGLEGPVVLVGESLGAGVARITRARSEHTLRTCQLAGIAAAVGTLLNAPFAAALFALEVVYGNRIVYRKLAYCLLAGIIAYALNNRLLGFKPIFVAPPHPHTYTLGEYGLTALVAVAVSAPIALLFGLTMKHTRQVVERVSPVLRGAMGALCTVLVAGGLYYGAGMDFRHVLGMGEYTIAQLLADTPGPLSLWWYLLLIVGGKLLTTGFTVQSGGSAGMLIPSMVLGGVSGAATAQMLASVTGTGPADVTVFVVVGIASALVAVVGVPLAAIALVLEVFGSAYGPPAVLACCVTYVLTLRLSVYNEQRRVQAVAAEPVASD
>NZ_CP017169.1|WP_140853130.1|1166246_1167338_-|hypothetical-protein
MKKHASLSSLPALGRMLALAAMALLALPACGDDGATDEQLQASEDQRRQLEQQVSELEEEVTRLEAQVARQQLDAEAAQAELADITQQLEEARELLASQDWEGVYQQLTQVRAELAALRTQLAAMDGSLELNAAFVFGTAPFALGQTYATAGGGTVTFSQIRYWLSNVTLLKQDGTTRALTDSYHLMEVINAQELDGTSTPVTLPANRRERVQARAVPAGTYSGIRFSIGVDPTYNDDLSRQAGELHVLQNMASVSWMWFSSYIFTKTHGTYVTALGTQGDFTWDTGTNANYRTVELPFPTAVTVNSQKRLAVNLQANVEALFASLNPSTTPSIGATQSTESATLSDGFANMFALVSVENADR
>NZ_CP017169.1|WP_140858186.1|1165173_1166211_-|methylamine-utilization-protein
MAWLLLGACGERVPPPVEEGPFPRHLPVGMTVIPSPPDNPLTPEGIALGRWLFHSPRLSSNGQVSCATCHEQTRAFADDAALTRRGVSGRPLVRHVPALINLAWMEGLFWDGGSKNLESLSLAPLTHPDEMGNSQLSSMMARLSSEPEFAQRFENAFGPDGLTLSNLLRALAQFQRTLVSADSRYDRWRRGEPGASLSPQEQHGLALVQRHCATCHATELFTDNAYHNNGLDSDAAFGEGEAESRGRGRVTQRAEDAGRFKTPTLRNVPVTAPYMHDGRLATLEDVLEHYRGGMVASTTLDAAFQREGPSPGLSLDDAEKDAILAFLHALTDEPFLTASELAPPP
>NZ_CP017169.1|WP_140853129.1|1164021_1165161_+|di-heme-enzyme
MVWRVGRRAGVLAVLAWLGAGCGGTDGEAESYVWKLPMGFPTPRVPADNPMTEEKVQLGRRLFFDVRLSRNETQSCASCHDPARAFTEPLVTSQGSTGETHRRNAQGLANVAYATSLTWANPSLSTLEAQALVPLFGKEPVELGFGDREEELLGRLRAVPELAAEFQRAFPEAVEPVSVATLTRALASFQRSLISGNSAYDRYVYGNEVEAMTRQQKRGMELFFSERLECDHCHTGFNFQDATVHEATSEPILPFHNTGLYNEDGQGAYPAEDPGLIELTGRPEDMGRFRAPSLRNVAVTGPYMHDGSLATLSDVLDHYAAGGHARLVSGGETSPLQSGFVRGFTLTEQEKEDVLAFLESLTDTEFLTDPRFSDPSTVP
>NZ_CP017169.1|WP_140787776.1|1163088_1164009_+|metallo-mystery-pair-system-four-Cys-motif-protein
MPRSPPVGIALRGDSIPRESAMVFAHRRAVRMLPFALLGVLGCGDDMEVAIPFEARVGSEPFACGRTYTGVGTTGTTYEPMDLRVYLHDVRLVTAEGTEVPLKLEQDARWQVEGTALLDFADKTGLCTNGTQATNLRITGTAPEGNYTGLRFKLGVPETQNHLDVSTAPSPLNDTSLYWGWRSGYLFTRIEGRTTGLPGGHVMHLGSTDCAPPPEGQTNGTAGCTFGNRPEVALDSFDLASGKVVLDLGALFSGSNLDENAAVPNTSVGCMSQQTDPDCAPVFSRMGLTHRSQEGAPGPQAFIKAE
>NZ_CP017169.1|WP_174258650.1|1162113_1163037_+|GIY-YIG-nuclease-family-protein
MRTVVSLHECKVRASLLLKELASTDASRAARAAERLRVLPGFAGLPLGEVLARKDSVQRKHALAVIAREQGHATWVDLKQVRELDFEHLLAHVGGAHLNRWFSSYAEAADSLRALGGFLFPFREQFFVCEASLVEALGVDPADADWSCTGRDWMAPRDGAAQARLAQRFVRHSPSHASTSPDTRSPMSADSRRSELKRSYREAPPPMGVYAVRCLANGKVLVGASANVQGMLNRIRFELSTGMDRLPTLLEDWKRYGAERFTFEVLDVLKPSDEPVVAPEEELKVLEALWLDRLKPYGDAGYNVQGG
>NZ_CP017169.1|WP_140853127.1|1161331_1161946_+|sigma-70-family-RNA-polymerase-sigma-factor
MGKECGVTETGQLSDEVVRALVDNHRQFLAFLERRVGSRAIAEEILQAAFVRTLEKGGALKEGEGAVAWFYRLLRNALVDHYRRQAAEGRALEREAQEAEGATVDTELKQAVCACVGELVPTLKPEYADILRQVDLEERGVPDVARESGITANNAGVRLHRARQALKKQLERSCGSCAAHGCLDCSCKPSHRAGGALVSGSTDV
>NZ_CP017169.1|WP_140853126.1|1158249_1160745_-|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I
MSSTSLQVMKFGGTSVGSPTRLRQVVELIGTHARQGPLAVVVSAMGDTTDWLLDAARLATEGDLEGALAVATRIADLAKANAAALAPGQATALAERVDGLLAPLRQLLQGVSLTRECSAPTRDRVLSFGELVSATLLAELLTAHGTSATFRDARQLLVTDDRFGAARVDLVRTRERLQAARETWGVEVPVLPGFIAATPDGRTTTLGRNGSDYTAALVAQGLGASEVTVWTDVLGLHTADPELVTDAYPVAHLTHGEGLELAAVGARMLHPRTMIPLIESGISLRIRNTMEPEHPGTLIDAIGSRDGQRPACIATREDLALLGIEVRKLSDQFQLGERVLAALREARVTVWMTAQSANGQSLAVVVPRPDAEHARSVLAAELALELSRREVEPLEVRQPVTLLTLVAEAMGHGVNVAGRFFSALGAVGVNVRASAQGASSRSLSCVVDAADTAIAARTTHAAFNLAHQQVSLFVLGRGTVGGQLMAQLRAQQTLLRDRHGIALRVVGLADSKRALFDAAGLALDGVEARLEGVTPEAPQARTLVPLLDALRRLPVPILVDCTAAGGLEALYTEAFQRGIHVVAANKKPLALPWEAREALVDTARRNHVAYHYETTVASSLPVIDTLANLVRTGDTVRLITASLSGSLGFICNELTAGVPLSRAVRTARERGFTEPDPREDLSGTDVARKALILARELGLPLSLSDVALEPFVATDECASVDSFFQVLATQDAAYAERVARCRHAGTVLRYLARIDPSKAGTGSPVIRVGPVGVEAGHPAADLRGSESFVSFTTTRHSDFPLTVRGAGAGGAVTASGVLADILRISQTLRGR
>NZ_CP017169.1|WP_140853125.1|1157123_1158224_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MKLATALVHAGVRRDPTTGAVAVPIYQSATFQHPALGQSTGYDYSRTRNPTRSALEDALAQLEGGSRGLAFSSGMAALHCALQLFGPEDHVLLTEDLYGGTYRLVDRILHVPCTFVDTSRPGAVRDALRPNTRAIVVETPTNPMMRTADLSELAAIARKAGVLLIVDNTFLTPWLQRPLELGADIVVHSATKYLAGHNDVVAGALVVKDAALGERLAYFQNGIGAILGPQDAYLVIRGLKTLALRMERHQANAREVAAWLRAHPGVERVFYPGVGGMLSFTVAHAALVPQVLASVQLCLFAESLGGVETLITYPTTQTHADIPAERREALGISDRLLRLSVGIEDSHDIIADLAHALRDPFAAHGA
>NZ_CP017169.1|WP_140853124.1|1156054_1157185_-|aminotransferase-class-V-fold-PLP-dependent-enzyme
MTSSPTWPTRFATRLLHTGHEQDPTTGAAAVPIYQVSMFDQPGLETPGEFDYARSGNPTRKALEGVLAALDEGHAAFAFGSGMAAVSSVLMLFSAGDHVVVTDDCYGGTYRVLTRVFSRFGLQATFVDTSDPDAVRAALRPNTRALLVESVSNPFLKRTDIPAMARVAQAHGALLIVDNTFLSPALSRPLTEGADIVIHSATKYLGGHSDVVAGAVVVKTPALAQELGFLQNAVGAVLGPQDCFLLQRGIKTLQVRLERQVRTAGALVKWLTGRPEVRQVFYPGTGAVVSFRLAQDTLAAPFVESLQLPLLGVSLGAVESIITVPARHSHASVPAAERERRGITDGLIRFSVGLEDLEDLQEDFVRAFTQAGRVAA
>NZ_CP017169.1|WP_140787784.1|1171584_1171998_+|four-helix-bundle-copper-binding-protein
MASVEVMNADSEMRQCIEDCLACHRVCLETLTYCLGKGGKHAEARHLRLLMDCAEICQTSANFMLRDSELHSRTCFACSEVCGRCAESCAQMGEDVVMKACADMCTQCSDSCWRMGGGVMSQTPNPEAAQRAADLPA
>NZ_CP017169.1|WP_140787786.1|1172086_1173178_+|Rieske-2Fe-2S-domain-containing-protein
MSSREEGRTSGTPAGHISVVHLPNAWFILCASSELGDKPLARTLQGSPLVLFRGEGGKPAALVDRCPHRNVPLSLGRVQEGQLQCGYHGWRFDGAGQCRAIPGFLGEPGARARCATAHATREQDGFVWVYSTPGVEPTTEPYRFPLLEAREYTTVRRTLRAPGSLHSTLENTLDVPHTAYLHGGLFRTEEKRNEIDVVVRRSADKVEAEYIGEPRPSGLVGRLLAPGGGVVQHFDRFLMPSIAQVEYRIGDTSHIMVTSAMTPVSDWDTLVYAVVTFRLPLPRWLVRAALPLIMPVALHIFGQDARILRQQTETIRRFGTEAYASTEIDVLGPGILRLLRAAEREKPGAVGDTVHETRLKMRT
>NZ_CP017169.1|WP_140787787.1|1173329_1174211_+|hypothetical-protein
MRFPVRAALAGAALLFAPQALATNYTLWIHGKNSGGTKPGNYADFSAWGPASTAAGVNKKAVNWDGRQRIGGQNERIRDALDCYCTGDNWCYIAVHSAGNLQIGYALALYGGSARYKKNATPNASGVCGNTDGKTQTGWNIKWVNVASGAAGGSELADMGEWAVDDPIVSDLKTTTARAMYNHNTTRGIRFNMYAGAKGKVYSGLLPGQDDDAVSYHSTGGVSGSAGGAYCNPSDWFCNDLTTGANACEGGQAKWTNHFVAFRDDAESHGHGANGKWEGIVGKVRADMVTNAK
>NZ_CP017169.1|WP_174259034.1|1174271_1177394_-|efflux-RND-transporter-permease-subunit
MNRILRSSFARPGLTVMLALALSAFGAVALQGLTRDVFPDLSAPIFNVIVQNPAMGAQELETAVAIPMEVALAGLPEVRRIRSTSQLGVTQLTVEFEPDADYFRSRQYVVERVAQAQSELPPGTDAPLVSSLTGRLNEVFEFTLEAEPGAAELMTLRDLAEFEVKNRLLAVPGVAGVERLGGYLRQFQVQLDPDQMVARGITLNQVEHALEGANLNASGGFVVQGPMEWTVRAVGRAESVEDLRDTVVAVRDSTPVLLGDVADIREAPAVRRGIAHRLKGEVVSCRVIKQFGADTQRVTAGIRVAIQELKQGLPPGVQLRIVYDQSVLVDSALGGVSRAILLGAVLVVLVLFLLLGDWRAALIVTLTLPLSLALAGVLLKFAGIGINTMTLGGLAIAVGLLVDAAIIVTENIVHGLREAKGQRSRREVALAASMEMARPIAFATLIVVSVFIPLFAMTGIEGRMYQPLAAAVVACLTASLGLALTLVPVASGLFLRTPREGQPEDVWVIRKIKHVYAPMLEACMRHAGLVRLVALAITVPALSLAFVVGSDFMPKLDEGALLLQTVLPPEASLEEVDRLNHLVEDALLKFPEVEDVVRRTGRAERTEDPMPHTLSDVLVILKPERGRSMEDLEAAMREAVGQVPGVSTLFTTPLGMRIDEGLGGSPADLSVRIFGPELETLAGLAERAQAIMSKVEGVEDLRAEKLTGLPQLRITVNRAAVARVGLTPGDVIHAVKVGMVGQEFAQVWKGQRRYDLLLRLADHRRGDATAIRGLLVDGHDGTRIPLSQLATIEETFGAGSIRREAGSRRIAVEASVAGRDLGSTAAEVRERLAAELKLPTGYFLDVGGKVESQQRAAQAMTVAIAVALLAVFILLYLALGSLAESLVIIATLPDAFVGGILALLIAGETWNVSSLVGLIGLFGIAVQNGLVLVAQTKLLMQHGKPFDEAIREASIGRVRPKLMTAGTAILGLLPLLVLPLHGTEVERPLAVVMVGGLVTSTLFTLLVLPTFYAFVHGWQVRVTQRLAARKAARTQTPGEH
>NZ_CP017169.1|WP_140797341.1|1177410_1178610_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MKPLHAAVAALFLLTACKRETPHDEQEHGHDEPPAQAGAHHDDHGVPHVRIASEMLRDLRITTAPVGVRPGGENVTVLGELTFSEDAYAEVASPIAARVSAVFVTTGQEVKQGEKLADLRSPELGKARASLQAAQAQAQAARQAAERKRTLADERIIARKDVQAAEAEAAAAEASVAAARAELVALGVSEEELRGGNVPPGFVLRAPLSGTVVERTARMGQMADPNLPLFCIGDVSSLWLVVHAFERDAVRIQRGTQARITFAAFPGQEFMAKVGHVGQRVDATSRTIPVRLELDNADGQLRPGMSASAYIPLGDPGAPITAVPAAALQRLEGGWVAFLPTDARGVFERREVGRGRTLGGDVEVLTGLKPGEQVVVEGAFLLKAEAEKLSGGGSDGHAH
>NZ_CP017169.1|WP_140787793.1|1178606_1179869_-|TolC-family-protein
MPHPLTVAAFGLAATLLFPRVAAAQPGSADAALSLEETLALARQRAPALLEAAGRAAEAQGPVAAAASLLNDNPTFELQAGPRSDPGSPGHPAVRGVDLSVGISQSFELGGKRGARRESARAGLEMETARQRDAERRVLGDVAARFLQALHARERLSLAREAEAAARETANSAQRRFEAGDVPVVDVNVARVSLARMRAEVATAEGDEAVQLHQLRAMLGLPLTHPFAIRGELRVLALQPDTEAKTNTVAARPDITALEAELAQADADRRMGRASVWPDITAGFLYQREIDEIAYLGALSVPLPLFDRGDNARVTGEARVRRLQSLLAAARLEVDVQVEAARVQHRKRLEAVTLLEADALPLLSDNESLARRSYEAGEMGLAEFLLVRRDTLEARAAYLDSLLQAALARVQLAVETGALP
>NZ_CP017169.1|WP_140787795.1|1179978_1180293_-|hypothetical-protein
MLRIWLIVCLFLFAPGLGGLMPTLTGAVGEVCTQSCPDDDDQGQCAPDCIDCTCCSHVRSVAAHAPPPSFVLLVSRPLRVAYEKAEPLSADGGDILHVPIAPLA
>NZ_CP017169.1|WP_140787797.1|1180382_1181228_-|N-acetylmuramoyl-L-alanine-amidase
MSLRLPSLSSVFRATQAQAPRTAAAAAATVSAPPAGLRKGDSGPKVKQLQDALVKVGYMTKAQVTTGPGSFGPQTETAVKKFQADNKLPATGFYGDLTHAALKKALGTSGPTTPTTPGGKFTKPAVINAPSPNQNSRGGTKIDTIVMHHTATNNGAGDLSWMRNPQSKVSAHYMVDRDGKIYQLVGDDKRAWHAGKGELHGVPSDINNRSIGIEIVNDGSGKTPFTEAQYKSLTQLTGYLKQQHNIPMKNIVGHADVAVPKGRKNDPAPNFDWNRLRKGIS
>NZ_CP017169.1|WP_140853133.1|1181348_1184549_-|CusA/CzcA-family-heavy-metal-efflux-RND-transporter
MQPTEHGEQGFIGRIIGACARNPFLTILLVGALAAWAVHAVRNTKLDAIPDLSDTQVIVFTEWMGRGPDLVEDQITYPISSSLLSAPKVKAVRGQSMFGMSFIYVIFEDGTDMYWARSRVLEYMETARGRLPAGVTPMLGPDATGVGWVFQYALVDESGKHSLADLRSLQDWNVRYALSSVPGVAEVASVGGIVKQYQVQVDPNQLRAYGVTLGEVTRAVRESNEDVGGRVMEIAGHEHIIRGRGYIRSTQDIENIPLKVSGDGTPVLVRNVATVSLGPDIRRGVAELDGKGEVAGGIVVMRYGENALTVIEAVKERLEEVRAGLPEGVELVVTYDRSGLIEESISTLSRALVEEMLVVSLIIFLFLMHARSALVTIFTLPLAVLLAFIPMYYQGLTANIMSLGGIIVAIGAMVDASIIIVENIHKKLEAWEAEGRPGERREVIISAMQEVGPSIFGTLLVLTVAFLPVFTLEATEGRLFKPLAYTKTYSMGFAAVLAVTLTPALAVLFIRGRIRREDENPLNRWLVALYMPVVRFVVRHAKVVVALSVVAMAMTIPAFMRLGHEFMPPLNEGAILYMPTSPPGMSITEATRILQSMDGELKRIPEVVSVFGKAGRAETATDPAPLSMFETTVVLKPKSEWRKGLTWEALLAEMDETLQYPGMPNIFWMPIQTRTEMLATGIRSPLGIQVFGDNLDTLEQAAVAIEKAVAQVPGTRSAFADRSTGGFYVDIGVKREEAARLGLGVKDINEVVMGAIGGENVSQTVEGRERYPINVRYAREYRDSPELLKEVLVPTPAGAQVPLAQVADVRFVQGPPMIRSEGGKLVTYVFVDTARPIADYVKDAKAAVAREVKTPTGVRVEWSGQFKYFERATEKLKVVIPVTLLLVCLLLYFSTKSVVEMGIVLLAVPFSLIGAVWLLYLLDYNMSIAVWVGLIALAGLDAETGVVMLLYLTLAHKKADQEGRLRSMADLTETIVDGAARRIRPKLMTVMTDMIGLLPVLWSTGTGADVMKRIAAPLVGGLVTSFLLELTVYPAIFALWKRRHLPQEQPEEGTGEPPLPAETQTA
>NZ_CP017169.1|WP_174258651.1|1184535_1186269_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MSPPNRRRIAPWLGVLTLAVLAAVAWRPLAGWFFGTTSHTGTAPATHDAHGRAGTPLPDAALEYTRAAFEAYEGARALLAQDAVEGLAARAGELKAALQQAAEATQGDGTPLKAWLQQGADGASHLAAAKDAEAARQHFARVSEALIALAFADPRLQEDWHVFECPMVDGVNQWLQREPKLENPYMGRRMLACGTTSEWRSAAPAGAHGEGDIAHYTCPMHPSVKQHGPGACPICGMDLTPVSRAELESGIIRVDDLRRQRIGVKTAKVAQAPMDLSLRALGRVTFDEKSLVDVTLKLDGYIHELRVNATGEPVKKGDVLFTLYSPELYAAQQEYLLARQSQSAANASLVGAARKRLELWGLSAAQIERVAQRGQPVENMPFLAPASGYVMEKNVVEGAAVKAGERLFRIAPLAKVWVEADVYEQDLARVKPGQPVEVTLPYLPGKKYAGHVGYVYPSLQGATRTGRIRIELPNPELELKPDMYADVRFVLQGGARLQIPDSAVIYTGPRRLVFVDLGEGRLRPQEVKLGIRGEGTYEVLEGLSPGDVVVTSGNFLIAAESRIRSATDSFGGSHAAH

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Crispr_ID: NZ_CP017169_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_5

1410814-1410892

Orphan

Consensus_repeat	Method
CGGGGGCTGGCTTCACCAGCGCGCCGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_5

>merge|NZ_CP017169|5|1410814-1410892|CRISPRCasFinder
CGGGGGCTGGCTTCACCAGCGCGCCGCCTTGGCCTGCGTGCGGGGTGATTCGCGGGGGCTGGCTTCACCGGCGCGCCGC

>NZ_CP017169|5|5|1410814-1410892|CRISPRCasFinder
CGGGGGCTGGCTTCACCAGCGCGCCGC	CTTGGCCTGCGTGCGGGGTGATTCG
CGGGGGCTGGCTTCACCGGCGCGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140788096.1\|1403562_1404153_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|225113
NZ_CP017169.1\|WP_140788102.1\|1405484_1406915_+\|MCP-four-helix-bundle-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_174259038.1\|1411434_1413042_+\|L,D-transpeptidase-family-protein	unknown	unknown	gnl\|CDD\|341130
NZ_CP017169.1\|WP_140853205.1\|1416054_1417287_+\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|272913
NZ_CP017169.1\|WP_020478251.1\|1420679_1420841_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140788108.1\|1413462_1414197_-\|dienelactone-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223477
NZ_CP017169.1\|WP_140796359.1\|1408603_1409029_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|176862
NZ_CP017169.1\|WP_140853202.1\|1408270_1408597_-\|TerB-family-tellurite-resistance-protein	unknown	unknown	gnl\|CDD\|143581
NZ_CP017169.1\|WP_090484863.1\|1406911_1408255_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017169.1\|WP_140853206.1\|1417290_1418502_-\|lipase	unknown	unknown	unknown
NZ_CP017169.1\|WP_140788098.1\|1404439_1404673_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237030
NZ_CP017169.1\|WP_140853203.1\|1414199_1414949_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|365914
NZ_CP017169.1\|WP_140788094.1\|1401593_1403447_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017169.1\|WP_140853204.1\|1415138_1416101_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_011551294.1\|1413045_1413459_-\|YjbQ-family-protein	unknown	unknown	gnl\|CDD\|376651
NZ_CP017169.1\|WP_140853201.1\|1397728_1401508_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP017169.1\|WP_140788100.1\|1404971_1405439_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP017169.1\|WP_140796361.1\|1418404_1418755_+\|adenosylmethionine-decarboxylase	unknown	unknown	gnl\|CDD\|376892
NZ_CP017169.1\|WP_140788106.1\|1409115_1410699_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223959
NZ_CP017169.1\|WP_140853207.1\|1418751_1420647_+\|DUF4178-domain-containing-protein	unknown	unknown	gnl\|CDD\|379368

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140788096.1\|1403562_1404153_-\|GAF-domain-containing-protein	gnl\|CDD\|225113	COG2203, FhlA, FOG: GAF domain [Signal transduction mechanisms].	2.58306e-10
NZ_CP017169.1\|WP_140788102.1\|1405484_1406915_+\|MCP-four-helix-bundle-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.03263e-38
NZ_CP017169.1\|WP_174259038.1\|1411434_1413042_+\|L,D-transpeptidase-family-protein	gnl\|CDD\|341130	cd16913, YkuD_like, L,D-transpeptidases/carboxypeptidases similar to Bacillus YkuD. Members of the YkuD-like family of proteins are found in a range of bacteria. The best studied member Bacillus YkuD has been shown to act as an L,D-transpeptidase that gives rise to an alternative pathway for peptidoglycan cross-linking. Another member Helicobacter pylori Csd6 functions as an L,D-carboxypeptidase and regulates helical cell shape and motility. The conserved region contains a conserved histidine and cysteine, with the cysteine thought to be an active site residue.	2.40245e-30
NZ_CP017169.1\|WP_140853205.1\|1416054_1417287_+\|peptidylprolyl-isomerase	gnl\|CDD\|272913	TIGR00115, tig, trigger factor. Trigger factor is a ribosome-associated molecular chaperone and is the first chaperone to interact with nascent polypeptide. Trigger factor can bind at the same time as the signal recognition particle (SRP), but is excluded by the SRP receptor (FtsY). The central domain of trigger factor has peptidyl-prolyl cis/trans isomerase activity. This protein is found in a single copy in virtually every bacterial genome. [Protein fate, Protein folding and stabilization].	7.6673e-34
NZ_CP017169.1\|WP_140788108.1\|1413462_1414197_-\|dienelactone-hydrolase-family-protein	gnl\|CDD\|223477	COG0400, COG0400, Predicted esterase [General function prediction only].	1.4196e-32
NZ_CP017169.1\|WP_140796359.1\|1408603_1409029_-\|hypothetical-protein	gnl\|CDD\|176862	cd07820, SRPBCC_3, Ligand-binding SRPBCC domain of an uncharacterized subfamily of proteins. Uncharacterized group of the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands. SRPBCC domains include the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), Class I and II phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of the superfamily include PYR/PYL/RCAR plant proteins, the aromatase/cyclase (ARO/CYC) domains of proteins such as Streptomyces glaucescens tetracenomycin, and the SRPBCC domains of Streptococcus mutans Smu.440 and related proteins.	9.40365e-06
NZ_CP017169.1\|WP_140853202.1\|1408270_1408597_-\|TerB-family-tellurite-resistance-protein	gnl\|CDD\|143581	cd07177, terB_like, tellurium resistance terB-like protein. This family consists of tellurium resistance terB proteins, N-terminal domain of heat shock DnaJ-like proteins, N-terminal domain of Mo-dependent nitrogenase-like proteins, C-terminal domain of ABC transporter ATP-binding proteins, C-terminal domain of serine/threonine protein kinase, and many hypothetical bacterial proteins. The function of this family is unknown.	0.000269965
NZ_CP017169.1\|WP_090484863.1\|1406911_1408255_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	0
NZ_CP017169.1\|WP_140788098.1\|1404439_1404673_-\|hypothetical-protein	gnl\|CDD\|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.54493e-08
NZ_CP017169.1\|WP_140853203.1\|1414199_1414949_-\|peptidylprolyl-isomerase	gnl\|CDD\|365914	pfam00160, Pro_isomerase, Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD. The peptidyl-prolyl cis-trans isomerases, also known as cyclophilins, share this domain of about 109 amino acids. Cyclophilins have been found in all organisms studied so far and catalyze peptidyl-prolyl isomerisation during which the peptide bond preceding proline (the peptidyl-prolyl bond) is stabilized in the cis conformation. Mammalian cyclophilin A (CypA) is a major cellular target for the immunosuppressive drug cyclosporin A (CsA). Other roles for cyclophilins may include chaperone and cell signalling function.	2.00384e-59
NZ_CP017169.1\|WP_140788094.1\|1401593_1403447_-\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	6.04612e-94
NZ_CP017169.1\|WP_011551294.1\|1413045_1413459_-\|YjbQ-family-protein	gnl\|CDD\|376651	pfam01894, UPF0047, Uncharacterized protein family UPF0047. This family has no known function. The alignment contains a conserved aspartate and histidine that may be functionally important.	2.29223e-54
NZ_CP017169.1\|WP_140853201.1\|1397728_1401508_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	2.15161e-10
NZ_CP017169.1\|WP_140788100.1\|1404971_1405439_+\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	0.00107892
NZ_CP017169.1\|WP_140796361.1\|1418404_1418755_+\|adenosylmethionine-decarboxylase	gnl\|CDD\|376892	pfam02675, AdoMet_dc, S-adenosylmethionine decarboxylase. This family contains several S-adenosylmethionine decarboxylase proteins from bacterial and archaebacterial species. S-adenosylmethionine decarboxylase (AdoMetDC), a key enzyme in the biosynthesis of spermidine and spermine, is first synthesized as a proenzyme, which is cleaved post translationally to form alpha and beta subunits. The alpha subunit contains a covalently bound pyruvoyl group derived from serine that is essential for activity.	5.65001e-26
NZ_CP017169.1\|WP_140788106.1\|1409115_1410699_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|223959	COG1028, FabG, Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) [Secondary metabolites biosynthesis, transport, and catabolism / General function prediction only].	5.52806e-12
NZ_CP017169.1\|WP_140853207.1\|1418751_1420647_+\|DUF4178-domain-containing-protein	gnl\|CDD\|379368	pfam13785, DUF4178, Domain of unknown function (DUF4178).	1.80914e-21

>NZ_CP017169.1|WP_140788106.1|1409115_1410699_-|SDR-family-NAD(P)-dependent-oxidoreductase
MKLAETAPTPAPEALPPPAPLSLDEVRRVTQLLEAISEDRFLLAGLPEEDRIAFLSAAGRVLHPDRDTKSRMAKALRRDRKKTKREHDRAIRATTEIRTLRRSAIFTVPALPPPPPSEAGPERILEQPRRCYVCKAEYRKLHFFYDAMCIECADYNYAKRTQRADLNGKVALITGARVKIGFQASLMLLRSGARVIATTRFPNDAAQRYVQEPDFADWAHRLHIHGLDLRHAPSVELFAKYIEQTHERLDILINNAAQTVRRPPGFYGHLLPGEMRRADDLPAAARALLAGHDACVSTVQPAALGAGKAGGSELATTWRSNDPALGIHSSAALSMLPYALEQEGDVRAIFPQGRLDADLQQVDLRDMNSWRLRLAEVQTAEMLEVHLINAVAPFILVGKLKPLMLRDRSSPGHVVNVSAMEGSFSRGTKTDKHPHTNMAKAALNMMTLTSAPDYARDNIYMNAVDTGWVTDEDPAQHAERKVQELDFQPPLDIVDGAARVVDPIIASENSGEYVWGNFFKDYRHTAW
>NZ_CP017169.1|WP_140796359.1|1408603_1409029_-|hypothetical-protein
MTSMKGISTEMHPYLRMTAPPGVTGLEDVPFEPGQPLFRSKLLLGGVLPVGWSDLTLRELEPGRRFVEESPMSAMRQWRHERRIVETHAGVDIIDQLDFEPRFGGRLAEAFIRRLFEHRHSVLRRALTPSIGGRASQEKPA
>NZ_CP017169.1|WP_140853202.1|1408270_1408597_-|TerB-family-tellurite-resistance-protein
MSPEEQFHVEVLKLLLQVATVDGRVAHSEIGHILDTARGMSVPLPELAALTRCLRNNEPLPPPNMGILRTNPSAVIREAKALIASEGSVHAAEIEMLRQIRELLGVIN
>NZ_CP017169.1|WP_090484863.1|1406911_1408255_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MSSARILVVDDDPQARDLLQRLLGPLGAVTQAPDPRRATERIAEGAFDLVLTDMAMPEPGDGLKVLHEVKAQLPDTPVVVVTAFGNIEGALDSIQQGAFDYLAKPFDVDAILRVARRALEQKRLVEENRSLRQQVERGSLMLVGRSPALLEVYKHVARAAASNVPVLITGETGTGKEMVARALHKRSPRMNGPFIPVDCGAITESLMESELFGHAKGSFTGASGARRGVFEEASGGTLFLDEIGDVGMKVQSQLLRVLQEGEIRRVGESVPVKVDVRVVAATNKDLKARVAEGLFREDLLYRLDVVHLHLPPLRERSEDIPALVEHFAGRHARGGVRPVVTPEANARLAAYDWPGNVRQLENVVARALALNVTGVLGPQDFPEPIGDASTPKMAGLAGDMPSLAELSRRYAAQVLQHVGGNKSEAARLLDVDRKTLYKLLEAPEAES
>NZ_CP017169.1|WP_140788102.1|1405484_1406915_+|MCP-four-helix-bundle-domain-containing-protein
MASSRIPIRGYRAGFFFVVVLLSAVTAFTLWTEVRTGSQVDGLVQEALERAGSIGRIRVDALSLEAAIEAHVRATGDAERRAADAVMEQILADIRASSEAYTRNLPQGEKALWYRFNAACQGLADQVRAAAIFSQRREAERARRHLAERIRPLAAELDALGGALEEENAAEARRLVNRLEDLRVRNTALGAGATLLAILLSSLVGWRVTSLLKRQEAIIQGQLEELGRHNQELDAFTRRVAHDLISPLAPLKGYLTLIRRTGAVNDAGALEMLAQCESSAVRMGELIEALLRFCRAGTRGESTVGELDTAVTTVLLEVAQTAAAQGVALERELEPGVAVDCPGQLLQVSARNLLTNAVKYSEGRPDPRVKVRVATEDGMAVLEVVDNGIGMAPGTLASLFQPFFRAPEVRGLPGHGLGLVTTKRVVEAHGGTLVVRSEEGKGTHVVVRFPRVVRPAAATSGSQATTASAGMRKVGT
>NZ_CP017169.1|WP_140788100.1|1404971_1405439_+|hypothetical-protein
MRFLCFATALAVLGTGCATGIPLERLEAQVLESDRWRREYEAERERAEAFALRMAQLESALERVRLERAEAEQGRAALLEELVRTEADRHALEEHNTQLLALEREVNELKELKEMHEELSDVWYESALERARRRLNNPPQPAALPAAGNVAPTVP
>NZ_CP017169.1|WP_140788098.1|1404439_1404673_-|hypothetical-protein
MKTVFAAALLAAATAFANTPAPAAEAKPAAVEAAPEAAEAPQAEEAKAEAAPEAKPAKKAKKPAKKAAKSTTATEAN
>NZ_CP017169.1|WP_140788096.1|1403562_1404153_-|GAF-domain-containing-protein
MIEAFSKVSEASKLLLEKGLGPSTGMEALSMVGHALGVDRAYILENRVQGTYGRFITDMRYAWAEPPTPSPLANPVMRAFSFREFAPGWVDMLEAGMVVACPTRDAPPMMKDLLERQGTQSILLCPINPSRQQWWGMVAFEDCRRPRAWKPEEVTLLKSLGRAVAASVRHGQMRSSLDQVRNSLRQAVSRTPVSGL
>NZ_CP017169.1|WP_140788094.1|1401593_1403447_-|protein-kinase
MSSIDPTAISRPRSPDIISGYHLDKLVGSGGMGEVHKATQLSLGRTVAVKLLNPELAKDPSFIARFQKEAAALAALSHPHIVSIVDKGKTDTTYYLVMEFVDGPSLRELIREPHLDVVGALRRMLQICRAIEYAHGRGVIHRDLKPENILLDQQAGGIAKVSDFGLASFLDDASPSSRYALTSTHVSMGTLSYMAPEQRVDAKSADARADIFSLGVILYEWLTGEVPLGTFDPPSRRKPGLDSRLDAIVTRCLKPDPEDRYPSVTSLIADLELLVPGSLPSLAPVKLTHLQRVRQGVRKVVRMALQAAAVLLVMAALAVLGREWLRSGEKPVPPQPGAALNADLGPPSPRSMPGRLETGSEKRTVSVGDGPDAPSLLVAGRPVEAEEKAIIFPPVEERSQSRVGRARVDVVGLDGDIAVLSARVRADAPPDTWKRRGYVMLYGPSLQAPSAALLLQGSTGRYVALIHDGAGAPLRLEWALGERRGTMLGLASPEGEAALELRVDADGVMQGYVGKGKDQRAIGEPLNLGPGWMEHFGDAPVPAFGCIEGTCRAEGFLYTVRRAPPPGTTAPVPDVPVTKAVVAAVPAKAVPAKRPPPPPPPKKQPAKAPAKSPPKRR
>NZ_CP017169.1|WP_140853201.1|1397728_1401508_-|tetratricopeptide-repeat-protein
MRTIRLGFAALALVTALTGCHRSTSTATPRVLESAAEQAQKGTQQARTLAFAGFHALLVAGDATLAQQRFDDAIARDAGDVYALAGQSLMARRAGRPDRALSASLEMVARAPTHPLAAVAARHVLDSVGTSRALDDDILRGVERALAAGATGEAAYLMRGARMSVAVVRGDAEARDAAMRQLGGVSEVSLVGPFSPFHVLAWDESTPVSQSGSLAGPFTGAFGPLPVRTVRAPDGRMDLTGEPGQGDLYVQAFDADVTEPGLYVARTVSGTSHQVLMDGAPLMERRAWERATSTVTARAVQLPAGKHRFVVRQLKGGTSGLLTFALLRVDGRPSGVRFSTATGAAPQAWGSKAEFSDETPGVFPTTEGLKTALHEEAGELLAVVLAVRDGLQRDADGARRLMASVDANTPALLWLRAEVASADRTVPSKVARGRATRDLESVLAKDPGNVAALLLRAELFLDEGQPTSAMDMLKTASEVAQPAGHPVFMLRARAALALEVEALAEESLAAALEAQPGLCEALTLQYSLARRRDAAERSDTLAASLNGCPGTVVRQAEHARTRGDMETATKLYSELQARDPSSISLANTLANLYVSKRRFDDATAVLQKLATVWPRNAELVKRMADVREYAGQPAEALKLREKALAMAGDDLTLRRTEERARTGRELLQAYAVDGREAIRAYEAEPVSGGSAAAFVLDAAAVRVYPDGSIVNRIHTVQKALEQSGVQEIAEVNVPRGAQVLALRTLKADGRVLEPENIEGKDTVSLPGVAVGDYVEVEYLLAEPPRGPAQPGFTASAFYFQIANQPNAWVTYTVVAPKGVGMKVDAHGMKVPEPKVDGDLEVFHFETRRVPPFIPEPDAPPSANEYLPFVIVGAGDTGNESLVKLYGDAFLERWLRTAEVDAFARKAAEGKSGLDAVKALHAAVMQRFSGRDASLSQTAASTVAQDRGSRLTVMKAGLDALGIPSRVVAVRTFNTDPSAYTFPQDALLPYAALRVEVPGTEPVWVDTSVRYGPFGELPELAMGEREAWLLPEPGRPLQKVQTPPLKETPGKEVKLALKLAEDGTLSGQGEETYSGFEAAQIAEAFNQLSAESRNQALQGAVARYFGGASLSSVKLENQEQVGAPFVLRYEFTVPRFGRMEGGQRMALGPLTFPAQLGRRFVQLSTRRTPLYIDTTEASRTQVTLSMPKGWKLADPQASLEANNAFGRFTRSEKQDGSTLSVTESLRVPRNRVMPGQYELFSGFTGDVDLIQTRELVLVKP
>NZ_CP017169.1|WP_174259038.1|1411434_1413042_+|L,D-transpeptidase-family-protein
MFAAWQRTAADAGTDGGVDGSAEAALSPPRRTPDDGATVARDEVPALTIDPALDDLAQSEEEEDTPGEEEVPPPEQLTVIPDELHPGEELVLGPDGEPLEDTGLVLEDVDPGLEPVSGAEDGGTYAVPFAPDAGSLRVRRSIVVRQEPRQDAPALGTVAQDMRVRWQGETAVRGPDCEAWIQIEPRGWVCERYLEPNFREPRVRELPKLREGELTPGIYARVVGKRVRAYPSLALARARRKGVLLKGSVSVQLRGQVRIRRRTYWRTTDGQYLEARVLREYRPSSFEGVNAEAIADLPPTFAWAQSRTRPTAAVEVRTAPDAKATRETVLPPRTLVAVKELSEDGHWVSIAEDQWVARDDLHVAWFSHAPPQVEPGSRWLDVDLDAQVLVAYEGERPVYATLISSGKQGTDTPEGLFRIWIKFAEADMTGSGTAGNDTYRVATVPWTMFFQDDYALHTAYWHDRFGQPMSHGCVNLSPKDARALYSWAAPQVPVGWSMVHATEDAPGSWIRIRGQARPTGKPRKVAVAATQVGAP
>NZ_CP017169.1|WP_011551294.1|1413045_1413459_-|YjbQ-family-protein
MFHAKELTVSSRGRGFTDITADVQRAVAESGARQGLCTVFLHHTSASLLLCENADPDVRRDLESFFSRLVKDGDPLFVHDAEGPDDMPAHVRTVLTQNALNIPVKDGRADLGTWQGVYVWEHRTSPHRRRVTVSVVS
>NZ_CP017169.1|WP_140788108.1|1413462_1414197_-|dienelactone-hydrolase-family-protein
MERALRHVATRLGELDCHVIDALPEGATPELVVVLSHGLGAPATDLVPLGPELMAFQPALADRVRFVFPGGPMAWAHGGRAWFPLPDAVMRGEQRDWEQFARDVPPGMPAARRALMSTVDALCAAMKLPYGRIVLGGFSQGGMVSTDVALRLDEPPAGLCILSGTLTSEPEWRTRAQGRTGLPVFQAHGRYDPLLPLGNAERLRDMFVASGLTVDFHAYDMPHAIVTEELEALAAFLAARLGGR
>NZ_CP017169.1|WP_140853203.1|1414199_1414949_-|peptidylprolyl-isomerase
MRTQFLTTVLLCLTLTACKDSDKKESTGGGTPPSATTPAKPTAPSAAEVPAAAPPAEAASGEWTKKVQAGQDVYATLETNQGAIVVRLFSKDAPKTVANFVGLATGEKAWTDPKTGQRVEGKPLYDGVIFHRVIPGFMIQGGDPTGTGRGDPGFNVEDEYQSGRTFDKVGLLATANVGRPNTNGSQFFITTSKPTYLNNKHTIFGEVLSGYDVVEKIANVQRDPRDKPLEPVVIQKIAMSDQAPAGSGN
>NZ_CP017169.1|WP_140853204.1|1415138_1416101_+|hypothetical-protein
MAPPIRRNEPRPVPTPPVTARPTPPPPPPPARAEARPAQADRFEDAHNRVTQAATGLRSVSDAAVATQVRDAFGPRRFGPVNLPGGNGPVVEGANTRLARGAGAVSLAANVAQLPTGAVETFRDVRDALRNPTEANVREAVGTASGTLSTGLMAARDGLNLAGNVSNYRAATDAARTAFTAAAPEASRAAANRVATTAANTALEGASRQVVRRAAAEVAERGLEGAARTAGTAARAAVQGGGTAVARAAGRFTPGLNVAIAAADTVAAVNTITDPNASAGKKITAGVTALGSIAAATNIPVVSQVGAAVSTVSGFIGSFF
>NZ_CP017169.1|WP_140853205.1|1416054_1417287_+|peptidylprolyl-isomerase
MRPSPPCPASSAPSSRKRRVVNLNAPGGFGPAGALCYPRGTERETMTTHDDSQGGRKNARSLAELHALGIMKKMPAALQLDSTEPVELPTVEAPSLEGVSVAQVAPAPLTEQELVDRFDALRRQHADVRERQPGEDVALEDDVLVDVLGFANNRLMPFSVRENWWVRVAADPGLPGFFESLAGAKVGQSVGIELTLPDTYPVEALRGQPARFLVSVKAARELKLLDDDSPELLSRLGMGSITDVMRKLGDDLAQARLADVDRLTQERVMDVLVDRTPVEVSAALVDEEIRRRWAEAERPILQRKDFQPDELQEALEGWLQDPLTRMDAAYRITLALVLRAIAERDGIQPDRAATDAMLEDLANFTGVNRQELGVAVKEDEALARRLYEMALRFSTIDHVMKKVTLTPAAA
>NZ_CP017169.1|WP_140853206.1|1417290_1418502_-|lipase
MSASKSAASAAASLRLPGTQPLASTSHSCPVVSFEILPSPDVLSRALPRVRPQVTPWRARRYVGARLGLPGTLPLEMTPSQPEAPHAPSTHAAAPSAITRLARTLRGLPPAERWWGPGCAGMAGWLKRAAQSLPPEDLTPRFHALLARVRQGLPVLPQEARRHQYVLVRGMLGDELPGYLLDNVQRLERRGLSVREAAVDTEGLLADNVAVLREVLRDAEYFGRSVVMVGHSKGGVECTATLALYPELRHVVRAVVTLQAPYGGSSIAHDLATTPRLRRLIDFAFPLLFHGVSRSVEELSYPQRQAFIQQHPYPADIPTVSLATSRLSRTSTLYSLQRYLHERYGYQADGMVTAVDAEVPGARVVRLHDMDHAEAALRGLPGMVRYHPGDLTEVMVALALETR
>NZ_CP017169.1|WP_140796361.1|1418404_1418755_+|adenosylmethionine-decarboxylase
MTTGQEWLVDASGCVPGSLKDAAALAALFEALIVVLDLKVVGQPQWHVFPEPGGITGLTLLAESHLGIHTFPEHGFAALNVYCCRERQRPDFEALLARHLGATACVVRELKRGVTA
>NZ_CP017169.1|WP_140853207.1|1418751_1420647_+|DUF4178-domain-containing-protein
MTQGKCPSCGAMVEFTAGSAQVVVCGYCQTVVARKGLDFESHGKIGSIVPTDSPLQLRAEGRYRKAAYTIVGHLQKDHGAGPWDEWYVEFADGRTGWLSESEGAFHLMFDMGPEEGVALEDLHPGERLHLRDRAWVIEERGHGRVVAAAGQLPSDVDPTQDAWYVDATGPKGTFLTLDFGTRGHSPEAFVGEALKLEQLGIPAGQLRPRVRKVELQQARCTQCNGNLELRAPDKTLRVACPYCGALLDARQGKLSFLRMLQKPSRPLIIPLGTKGKLDGAEWICIGYLERSCTVEGVRYPWEEFLLYNASCGFVWLMNSNGHWVFLKPLPAGDVSLSPDVAAFYEHRRYKCFQHVTAVTDKVLGEFYWTVRVGERAEASEYVAAPYSVNVDATDDEVSYTHGEYLEPEVVKEAFGLQEPMPQREGIAPSQPNPHQSGLRSVFVWTGLWILALFVLAAVLSLTAAKTVVLEEAVVIPPDATPGTPGAMHFSEPFELPKRGNMRVEISGTPFNEWLGIQGDLVNQDTNDVVLFYEELSYYRGNDGDGEWTESNMSASTYLSPVPAGKYALRTTASFAANPVRPRPMTYRVKLIHDTPNSSWFCFALGLMVVGPVVALYRSHSFETRRWAESNV
>NZ_CP017169.1|WP_020478251.1|1420679_1420841_+|hypothetical-protein
MKWFGGLVLLGYAALTISGWSPFTKEERDKVPGNVRRGPGGVLLWTGGYMGGK

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Crispr_ID: NZ_CP017169_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_6

1778656-1778744

Orphan

Consensus_repeat	Method
TCCGGAGCCTGATTTTCGGGCTCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_6

>merge|NZ_CP017169|6|1778656-1778744|CRISPRCasFinder
TCCGGAGCCTGATTTTCGGGCTCCGGACGCGTTTCAAAGCGAAGGCGCGAGAGGGGGCCGAGCGCTCCGGAGGCTGATTTTCGGGCTCC

>NZ_CP017169|6|6|1778656-1778744|CRISPRCasFinder
TCCGGAGCCTGATTTTCGGGCTCC	GGACGCGTTTCAAAGCGAAGGCGCGAGAGGGGGCCGAGCGC
TCCGGAGGCTGATTTTCGGGCTCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140788627.1\|1793018_1793495_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|183594
NZ_CP017169.1\|WP_140788616.1\|1775188_1776799_-\|DUF2088-domain-containing-protein	unknown	unknown	gnl\|CDD\|370728
NZ_CP017169.1\|WP_140788625.1\|1787193_1788213_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_011551641.1\|1776812_1777478_-\|HAD-IB-family-hydrolase	unknown	unknown	gnl\|CDD\|319796
NZ_CP017169.1\|WP_140788629.1\|1793649_1794369_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370549
NZ_CP017169.1\|WP_140788611.1\|1766999_1768229_-\|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl\|CDD\|234846
NZ_CP017169.1\|WP_140853338.1\|1779379_1782481_+\|malto-oligosyltrehalose-synthase	unknown	unknown	gnl\|CDD\|237737
NZ_CP017169.1\|WP_140788608.1\|1765931_1766474_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140788622.1\|1785768_1786155_+\|Co2+/Mg2+-efflux-protein-ApaG	unknown	unknown	gnl\|CDD\|180098
NZ_CP017169.1\|WP_140788612.1\|1768489_1769371_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP017169.1\|WP_140853337.1\|1770767_1775180_-\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|341240
NZ_CP017169.1\|WP_140853339.1\|1782477_1784619_+\|glycogen-debranching-protein-GlgX	unknown	unknown	gnl\|CDD\|131155
NZ_CP017169.1\|WP_140797540.1\|1786154_1787243_+\|ferrochelatase	unknown	unknown	gnl\|CDD\|366291
NZ_CP017169.1\|WP_174258684.1\|1769374_1769545_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140788610.1\|1766470_1766992_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379228
NZ_CP017169.1\|WP_140797537.1\|1777569_1778550_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187539
NZ_CP017169.1\|WP_140788614.1\|1769742_1770771_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187539
NZ_CP017169.1\|WP_174258685.1\|1789036_1792582_+\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223627
NZ_CP017169.1\|WP_011551643.1\|1778896_1779214_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366976
NZ_CP017169.1\|WP_140788621.1\|1784748_1785699_+\|TerC/Alx-family-metal-homeostasis-membrane-protein	unknown	unknown	gnl\|CDD\|274743

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140788627.1\|1793018_1793495_+\|hypothetical-protein	gnl\|CDD\|183594	PRK12558, PRK12558, glutamyl-tRNA synthetase; Provisional.	0.00358295
NZ_CP017169.1\|WP_140788616.1\|1775188_1776799_-\|DUF2088-domain-containing-protein	gnl\|CDD\|370728	pfam09861, DUF2088, Domain of unknown function (DUF2088). This domain, found in various hypothetical prokaryotic proteins, has no known function.	2.50008e-42
NZ_CP017169.1\|WP_011551641.1\|1776812_1777478_-\|HAD-IB-family-hydrolase	gnl\|CDD\|319796	cd02612, HAD_PGPPase, phosphatidylglycerol-phosphate phosphatase, similar to Escherichia coli K-12 phosphatidylglycerol-phosphate phosphatase C. This family includes Escherichia coli K-12 phosphatidylglycerol-phosphate phosphatase C, PgpC (previously named yfhB) which catalyzes the dephosphorylation of phosphatidylglycerol-phosphate (PGP) to phosphatidylglycerol (PG). This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	1.78812e-39
NZ_CP017169.1\|WP_140788611.1\|1766999_1768229_-\|glucose-1-phosphate-adenylyltransferase	gnl\|CDD\|234846	PRK00844, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_CP017169.1\|WP_140788629.1\|1793649_1794369_-\|hypothetical-protein	gnl\|CDD\|370549	pfam09535, Gmx_para_CXXCG, Protein of unknown function (Gmx_para_CXXCG). This entry consists of at least 10 paralogous proteins from Myxococcus xanthus and that lack detectable sequence similarity to any other protein family. An imperfectly conserved CXXCG motif, a probable binding site, appears twice in the multiple sequence alignment.	7.32089e-112
NZ_CP017169.1\|WP_140788622.1\|1785768_1786155_+\|Co2+/Mg2+-efflux-protein-ApaG	gnl\|CDD\|180098	PRK05461, apaG, CO2+/MG2+ efflux protein ApaG; Reviewed.	1.40881e-74
NZ_CP017169.1\|WP_140853338.1\|1779379_1782481_+\|malto-oligosyltrehalose-synthase	gnl\|CDD\|237737	PRK14507, PRK14507, malto-oligosyltrehalose synthase.	0
NZ_CP017169.1\|WP_140788612.1\|1768489_1769371_+\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	1.21077e-65
NZ_CP017169.1\|WP_140853339.1\|1782477_1784619_+\|glycogen-debranching-protein-GlgX	gnl\|CDD\|131155	TIGR02100, Glycogen_operon_protein_GlgX_homolog, glycogen debranching enzyme GlgX. This family consists of the GlgX protein from the E. coli glycogen operon and probable equivalogs from other prokaryotic species. GlgX is not required for glycogen biosynthesis, but instead acts as a debranching enzyme for glycogen catabolism. This model distinguishes GlgX from pullanases and other related proteins that also operate on alpha-1,6-glycosidic linkages. In the wide band between the trusted and noise cutoffs are functionally similar enzymes, mostly from plants, that act similarly but usually are termed isoamylase. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP017169.1\|WP_140797540.1\|1786154_1787243_+\|ferrochelatase	gnl\|CDD\|366291	pfam00762, Ferrochelatase, Ferrochelatase.	3.32436e-132
NZ_CP017169.1\|WP_140788610.1\|1766470_1766992_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	5.34732e-10
NZ_CP017169.1\|WP_140797537.1\|1777569_1778550_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187539	cd05228, AR_FR_like_1_SDR_e, uncharacterized subgroup of aldehyde reductase and flavonoid reductase related proteins, extended (e) SDRs. This subgroup contains proteins of unknown function related to aldehyde reductase and flavonoid reductase of the extended SDR-type. Aldehyde reductase I (aka carbonyl reductase) is an NADP-binding SDR; it has an NADP-binding motif consensus that is slightly different from the canonical SDR form and lacks the Asn of the extended SDR active site tetrad. Aldehyde reductase I catalyzes the NADP-dependent reduction of ethyl 4-chloro-3-oxobutanoate to ethyl (R)-4-chloro-3-hydroxybutanoate. The related flavonoid reductases act in the NADP-dependent reduction of flavonoids, ketone-containing plant secondary metabolites. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.71903e-53
NZ_CP017169.1\|WP_140788614.1\|1769742_1770771_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187539	cd05228, AR_FR_like_1_SDR_e, uncharacterized subgroup of aldehyde reductase and flavonoid reductase related proteins, extended (e) SDRs. This subgroup contains proteins of unknown function related to aldehyde reductase and flavonoid reductase of the extended SDR-type. Aldehyde reductase I (aka carbonyl reductase) is an NADP-binding SDR; it has an NADP-binding motif consensus that is slightly different from the canonical SDR form and lacks the Asn of the extended SDR active site tetrad. Aldehyde reductase I catalyzes the NADP-dependent reduction of ethyl 4-chloro-3-oxobutanoate to ethyl (R)-4-chloro-3-hydroxybutanoate. The related flavonoid reductases act in the NADP-dependent reduction of flavonoids, ketone-containing plant secondary metabolites. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.37177e-79
NZ_CP017169.1\|WP_140853337.1\|1770767_1775180_-\|AMP-binding-protein	gnl\|CDD\|341240	cd05914, LC_FACL_like, Uncharacterized subfamily of fatty acid CoA ligase (FACL). The members of this family are bacterial long-chain fatty acid CoA synthetase, most of which are as yet uncharacterized. LC-FACS catalyzes the formation of fatty acyl-CoA in a two-step reaction: the formation of a fatty acyl-AMP molecule as an intermediate, and the formation of a fatty acyl-CoA. Free fatty acids must be "activated" to their CoA thioesters before participating in most catabolic and anabolic reactions.	3.0807e-111
NZ_CP017169.1\|WP_174258685.1\|1789036_1792582_+\|DEAD/DEAH-box-helicase	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	1.35563e-99
NZ_CP017169.1\|WP_011551643.1\|1778896_1779214_+\|hypothetical-protein	gnl\|CDD\|366976	pfam02201, SWIB, SWIB/MDM2 domain. This family includes the SWIB domain and the MDM2 domain. The p53-associated protein (MDM2) is an inhibitor of the p53 tumor suppressor gene binding the transactivation domain and down regulating the ability of p53 to activate transcription. This family contains the p53 binding domain of MDM2.	1.90422e-31
NZ_CP017169.1\|WP_140788621.1\|1784748_1785699_+\|TerC/Alx-family-metal-homeostasis-membrane-protein	gnl\|CDD\|274743	TIGR03718, R_switched_Alx, integral membrane protein, TerC family. Rfam model RF00080 describes a structured RNA element called the yybP-ykoY leader, or SraF, which may precede one or several genes in a genome. Members of this highly hydrophobic protein family often are preceded by a yybP-ykoY leader, which may serve as a riboswitch. From the larger group of TerC homologs (pfam03741), this subfamily contains TerC itself from Alcaligenes sp. plasmid IncHI2 pMER610 and from Proteus mirabilis. It also contains the alkaline-inducible E. coli protein Alx, which unlike the two TerC examples is preceded by a yybP-ykoY leader.	4.36061e-152

>NZ_CP017169.1|WP_140797537.1|1777569_1778550_-|NAD-dependent-epimerase/dehydratase-family-protein
MRALITGAGGFLGTWLAKALAARGDTVTCLLRPGGDASGLAGVTCTRVDGDVTAPSTLAAAVAGQDVVFHLAGARRGATRDDFMRVNAEGTRHLCEAMVAAGHRPRMVLTGSLAACGPSTPTRPHVEEDAFHPHEWYGESKAEAERIAFSYGDRLPITVSRPPRILGPGDRENLPFFKMAQRGIRLELSGGPRPLTMVDVEDVVDILLLQATHPAAIGEAFFCAGPGEPLSLEKVQDMGAQALGLTPRTVRVHPAVLRALATAADGVSQLTGRKLALSRKMAKQLLAPAWTCSGAKAERLLGFHPRRDLADSIRRSVRWYQEQGWL
>NZ_CP017169.1|WP_011551641.1|1776812_1777478_-|HAD-IB-family-hydrolase
MSSKAAFFDVDGTLVKTNVVHVYAYYAMNRGSVLGIAGRTLSTALSVPLFGVMDAVDRKTFNEFFYRYYAGLSEDRLVTIAEDMFEDVLQPALFEQTQDLIDQARRSGCKIVLVTGALDFTMRPLARHLGADDMIANKMQFVGGKATGKVIPPIIEGANKANAIRAYCTKEGLSLDKCHGYSDSASDYAMLAVVGRPTAVNPDLRLRSIARAYNWPILDLK
>NZ_CP017169.1|WP_140788616.1|1775188_1776799_-|DUF2088-domain-containing-protein
MRPFKTLQKLYDEESQVVITEKGSPPRVLFHGENFLQEDLPVGTRVIFPRPPLAGVPNVKAAIRYAINNPEGMEPLHALLKPGMRLTCVIDDISVPLPPMVTPDVRQTILEIVLELAADSGVDDVHLIIANALHRRMTEGEMKRMVGEKIFDAYYPDRYYNHDAEDPDGMVALERTSHGEEVSVNRRVAESDLIVYVNVNFVPMNGGHKSMGTGVSNYASLRHHHNPKTIRASDSYMEPKTSALYKSNERIGRNIDKHLKVFHIETALNNRMFGGPTDFLAKKEEDYTEADRLKFQAMRFALSKLPRAAARKVLNSVPAPYDVTGVYAGATEPTHQKTLETSYKQYVVPVEGQSDIVIFPIPFISPYSVNSILNPLLVQVMGLGYFYNLNRGVPLVKKGGVLILLHPAYDEFDPEHHPSYIEFFHRLLPETRDSMKLEHKYEREFAENPSYVHLYRKGNAYHGVHPFYMWYWGENGRQHVGKVIVAGAENNHVPALMGWDRTDTLTEAIEEARGFMGRSATISLLRIAPTVMVDVK
>NZ_CP017169.1|WP_140853337.1|1770767_1775180_-|AMP-binding-protein
MAALPELNVTQTFTGKRLLFAGATGFVGKVTLSMLLTRYGQDLDKVYVLVRKGSAASAERRFFDKVATSEPFQPLRDSLGDEGALAFIRQKVEVLDGDITDPWMGLEEPQVEALTGKVHAFINCAGLVSFNPSLEVGLNVNTHGLKFAAALALRWSVPLIHMSTAFVAGNRSGLVFEDEEVRGYFPKREEMDGRDFSLEQELQDAARIVARLREQAEDRALTSTFRKKALDRLEEEGRDTNDEKTLRLAVGRERKLWLSGELVRAGMERAAHWGWPNTYTYTKSLGEQVLAATPGLRYSIVRPSIVESARHFPFPGWNEGFTTSAPLAFAGIKGPGGIPAGENTILDIIPVDQVAGATIGITAHAMDVEERRIYQLASGDENPFYAGRSVELVGLYRRRYYRNRESGNALMNKLRSRVEPQPVSKKEFELFSAPMLLRGARFLKKAIDEVRPAWGAPAVQAMLDKAKVSLDEVDDNAQGIIALTELFLPFLYENRYVFRCDNTRSVYARMAHADRLKVPWDPEHIDWREYFLGTHLPGLEKWVFPGMESEREKRTVIPAHRDLLELMEATVHAYRHRVAFRMVAGEKEERFTYGEVHRYAARVGSFLLAAGIKHGDRVLLVSENRPEWGINYFGILRAGATVVPVDPGLSEAELVNIARRAEARACLVSEDAARDFPGLFAALGDGVTVASLAEAMTGDPAYPDRIGPVRKSAAADDLASIIFTSGTTGTPKGVMLTHRNFAALVAKLAGTFDIGVGDGVLSVLPLHHTFEFAAGFLTPFWRGAEITYIDELTSDRLGEVFETGRITAMVGVPALWQLLHRKITQEFASRPPFIEQALKALMATHGELRNRNNINLGKLLFWPVHRKFGGRIKVIVSGGSALPDDVHKAFHELGFNITEGYGLTEAAPVLAVTKPGNKRQPGTVGRALPGIELRILNPDNDGLGEVLAKGPNVMPGYFGDREATEAVLKDGWLHTGDLGRLDAEGHLYLVGRAKDVIIDHNGKNIYPDELEELYQDHTHIKELSIVGLPDDAGGEKVACLCVPDYADRPREEVRRELEEHFRKVSAGMPFYRRVKVLRLWDGELPRTAKRSVKRKQVVEELKRQERMAASASKAREKAANPATGGIADWLFPLIADVSHRPVSDVRPDALLSGDLGFDSLMLTELSSALEAAGVPLPAVEDLTQVQTVEDLRKVVASSGKRPTVETRAKEISKENERAEEVEIPVPDVVADVGRQLLSFGQKVLYGGVFDVKVTGKSFIPQNRNFLVIANHSSHLDAGLVRVALGDQGERLVSLAARDYFFNTPLKRAWFENFTNLVPIERQGSLRESLRMAGEALRQGFNVLIFPEGTRSTTGELMEFKSTLGYLALTFNMDVLPLYIGGAFDALPKGSVLPKTKTPLRVNIGPVLGHADLRTRVQGMARSEGYRYVTRIAEDSMRALRDGRVLNLERVDLPPAGASPRASTSTEGKDS
>NZ_CP017169.1|WP_140788614.1|1769742_1770771_-|NAD-dependent-epimerase/dehydratase-family-protein
MKLLVTGGTGFLGTHLVPRLVAAGHEVRLIGRSQPSGAPYAGTEFVPGDLKNRDAVRRALEGVDAVYHLAGLVSFQPKDARKMFELHVDSTRELLRDVREAGVKRVVLASTSGTIAVSKEAHVRDESADYPITVVGQWPYYLSKIYEEKLALAYCRKHDIPLVVLNPSLLMGPGDDRLSSTWTVVKFLNREIPAMPGGGISFVDARDAADAFVQALTRGEVYGRHLMGVNLSMKDFFQRLERLSGVPAPKLKLPSKVNVLGGKLLERWAKVRGTTPTLDPQEIDIGEHWFWLDASKAEAELGFRARDIQETLSETVQHIYGKMPPQSLPGTKGRLAELRENT
>NZ_CP017169.1|WP_174258684.1|1769374_1769545_+|hypothetical-protein
MAASASEAGPSFLARLVLVLLGCVFLGAAWVWSHRAEPWAARLVDNARRTVGVPQR
>NZ_CP017169.1|WP_140788612.1|1768489_1769371_+|diguanylate-cyclase
MAGDETRVTKISTLNVHAHRSTECCLVQIHGPELGKKYLIEDAELTIGRDQHNHIVVDLDNVSRRHARILGRGGKMLVEDLGSTNGTFLNDQEVLQASPLRSGDLVKVGGSIFKFLDGDNIETQYHETIYTLTIADGLTGINNKRYFLEYLEKEMGRSTRYQRTLTLMMFDIDHFKQINDVHGHLAGDYVLRELAQSIKRLVRREQCFARYGGEEFAVVLPEDGPDKARLFAEKIRRLIAEKSFVYDEKEIPVTISIGVAEQTPDMLEPTHFIKVADANLYKAKKSGRNRVVG
>NZ_CP017169.1|WP_140788611.1|1766999_1768229_-|glucose-1-phosphate-adenylyltransferase
MSKVLAMILAGGAGTRLEPLTRERAKPAVPFGGRYRIIDFVLSNFANSGVYRMKVLTQYKSDSLNNHLSRAWRMTAFLGHYVEPVPAQMRTGLDWYKGSADAIYQNLNIITDEEPDYIFVFGADHVYRMDTRQMLDFHCAKKAACTVAAIPVPIEQGREFGIIDVGPDGRMRQFLEKPKDPPPMPGNPKMCLASMGNYLFSTDVLVQEVVRDAANETSAHDFGKSIISELYKRAPVYVYDFAQNEVPGQEAKERGYWRDVGNIDVYYQSNMDLVEVDPTFNLYNDRWPIHTQPNNYPPAKFVFADEQNSRVGHAMDTLVAEGCIISGGSVRRSVLSPKVRVNSYSEVEDSLLFENVTIGRRCRIRRAIIDKNVEIPPGMTIGFDPVEDRRRFHVTPGGVVVIPKGMKVT
>NZ_CP017169.1|WP_140788610.1|1766470_1766992_-|GNAT-family-N-acetyltransferase
MGADGLLLRPAKESDRRTLWRIHTLAVEALCPRAYAPHEVSTWVRLLKPEGYLRPERPRTVLVAERGRRAVGFGQVDAALGELEALYVVPDEAGHGVGPALLSALESAVWRGSAALLGLDASLNAEHFYQRHGYASVHSARRPLTVDVQLECVRMQKQRPTTALGRWPAWRRG
>NZ_CP017169.1|WP_140788608.1|1765931_1766474_+|hypothetical-protein
MACSPVSEWNGRAAGPLPARHFTRHRGELGTMENTYGAMNSPGGAGAKEAVSLPAILLMVLSAITVLLGLINVLQAFGGADPAVAEALNNPDLPEGAREMLSGMTSTGGQLLLALPTLVLNGIVFFGALKMKNLQSYGLAMAAAIIAVIPCCGPCACLGIPVGIWALVVLNKPEVKAAFT
>NZ_CP017169.1|WP_011551643.1|1778896_1779214_+|hypothetical-protein
MAAKKAAAKKAPAAKKAPAAKKRTPNASFMKEMTPSAALAEIVGAKPLPRTEVVKKLWAYIKKQGLQDAKNKRQINADDKLKPIFGGKKSVTMFEMTALVNKQLS
>NZ_CP017169.1|WP_140853338.1|1779379_1782481_+|malto-oligosyltrehalose-synthase
MLLDALEEEGSASNGAGGATMTAEALAEGLYARVQAELDARPHTPLSTYRVQFHKGFTFEDARQVVPYLARLGVSDLYASPYLKATPGSTHGYDCVDHQQLNPEVGTPESHAALCAALREQGMGQVLDVVPNHMGIERDNRLWFDVLENGPSSVYAKFFDIDWSPVKEELRDRVLLPILGDQYGIVLERGELKLSFRDGAFFLHYYEHLLPVAPRQYSRILRHGLERLESRLGGEHPGMLEFLSILTAIDYLPSRTEVERPKVVERHREKEVIKRRLAAVTAEFPEMLAYIEDNVRVFNGEQGNPRSYDLLDSVLAACSYRLAHWRVAGEEINYRRFFDINGLAALREEDPDVFQEAHALIFRWLREGLVTGLRIDHPDGLFDPTAYFLDLQEAYFVERAHALFLQTHAEDDTRWPAVESTLRERWRAEVTQQPNSRLRKALYVVVEKIQGGRERMPESWAVHGTTGYRYANAVSGLFVQPDAEKALTETYERFVGGQADFAELVYQKKLLIMRVSMASEINVLAHALNRISEMNRRTRDFTLNSLRRALVEFIALFPVYRTYVDGWRPELDGRDVQYIEWTIQRAKARNATTNASIFDFLRDVLLRRYPEHTDARERADMLRFAMKLQQVTGPVMAKGLEDTVFYIYNRLVSLNEVGGEPERFGVHANTFHLRNQERAERWPASQLTSSTHDTKRSEDVRARVNVLTEVPEEWRKRVKKWARQTEKAVSQLPSGPAPTANDTYLFFQTVVGAWPMGDSHSEEEMADFQRRVREYMGKAIKEAKVRTSWTNPDSAYDDAVARYVDACFDSKGAGSFLADARDFKRSIERAGQYNALGQLLLKMASPGVVDTYQGCELWDLSLVDPDNRRPVDFALRARLLEALDAEAEKDRAALSARLAANLEDGQVKLYVLAESLRLRQRQAALFRGGGYRALELTGARAKAAVSFAREHGDTVVVACAPRYTLSALQAPEGLAGAYGSTFLDLPEAYAGMMFRDVFTGRQVRPARGPGGAMLPLGPLLAEFPVILLERSAG
>NZ_CP017169.1|WP_140853339.1|1782477_1784619_+|glycogen-debranching-protein-GlgX
MRRAEVLPGKPYPLGATFDGHGVNFAVFSEHAKKVEVCLFDPEDPAKETRRFPLLETTHQVWHGYVPGLAAGTLYGLRVHGLYEPKKGLRFNPHKLLVDPYARAIHGQVDYQAPIYAYTPGTKEDDLAFDTRDDAAAVPKGVVMGADTFDWAGDAPPRVPWHDTLIYEVHVKGFTKLHPRIPEALRGTYAGLAHPASIEHLKKVGVTAVELLPIQHIVDEPFLIQREKVNYWGYNTLGYFAPDARYSGSGSMGGQVDEFKRMVKQLHRAGIEVLLDVVYNHTCEGNQLGPTLSFKGLDNAAYYRLTEKDPRYYMDVTGCGNSWNATHPYALKLIADSLRYWVEEMHVDGFRFDLATALGRDRYGYDTRAAFFQIIHQDPVLSRVKLISEPWDVGDFGYQVGNFPVLWSEWNGKYRDTIRRYWKGDDRQAAEIGYRLTGSSDLFSLSGRMPAASVNFVTAHDGFTLHDLVTYNDKHNEANGEENRDGANDNHSWNCGVEGETTDAKINALREQQKRNFLATLFLSQGVPMLVAGDEMGRTQKGNNNAYCQDNELSWVDWALSDTQRALLDFTCALTKLRREQPVLHKRRFFRGAHMWDSELKDLAWFRPDGKEMRKDDWEKPYVRSLGFLLGGDAITAPDDEGNRIVGDTILVLMNAHHEPITFMLPAVEWGADWELVVDTALAGESPRTHTPAGGTVQVVGRSLAVLRRPATE
>NZ_CP017169.1|WP_140788621.1|1784748_1785699_+|TerC/Alx-family-metal-homeostasis-membrane-protein
MNTQVALWVGFNVFVLAMLAMDLGLFHRKDHAVTPKEAGLWTLVWITLSLIFCAGIWHYQGPTVGLQWLTAYVVEYALSVDNLFVFLMVFSYFRVAPEHQHRVLFWGILGAFVMRAGLIIAGTALVKQFHWLIYLFGAFLVFTAVKMLVSKDEEIDPEQKGIVKFARRVLPVARLGEGSRFRVTEDGRRKFTPLFIVLLVVEATDLLFALDSIPAVLGISQDAFIIYTSNVCAILGLRSLFFVVASLMEKFHFLKVGLSAILGFVGVKMLITFFDIHVPIGISLGVIAGVLVAAIIASLVWPKQPEPGQDRESAKT
>NZ_CP017169.1|WP_140788622.1|1785768_1786155_+|Co2+/Mg2+-efflux-protein-ApaG
MSSSATTDGIRITVKPAYWPERSAPESGQFAFMYTVEIANEGDAPAQLKARHWVITDATGKVEEVRGEGVVGRQPHLGPGERFEYTSWAMLRTPFGTMRGTYDMVRPDGTHFDARIAEFALTLPNSLH
>NZ_CP017169.1|WP_140797540.1|1786154_1787243_+|ferrochelatase
MPTPTSKRGLLLVNLGTPDAPQTGPVRRYLREFLNDPRVIDIHPLGRWALLNFIILPVRPAKSAEAYRKIWMKEGSPLLVYSQALAAQVAERLAGEYEVVLAMRYGSPSIPDGIAALKARGVSEFTVLPLYPQEAASSTASSLARTYEVLAQSWDVPFVRAVPAFFEHPGFLDAFTAVARPVIDDARADYVLFSFHGLPERHMRKSDPTGTHCLSTASCCDAMTDANRHCYRAQSYATARGLAQRLGLPADGWSVSFQSRLGRTPWVKPYTDVVLPELAKKGVKRLAVMCPAFVADCLETLEEIGLRAREQFLEAGGESLTLVPSLNAHPAWVDAVVRMVRESDGPPTAVAGPSAPAPIPQR
>NZ_CP017169.1|WP_140788625.1|1787193_1788213_-|hypothetical-protein
MKQSVFGLVVALSLTACKEEPRGKMEPIPRPPGMKDAPPPAEAAPAAAAEPPVDPSKVVLRWKIAQGAPTSYRLDVERTGGAPASTEEVTPSKSAKGKGKEKPAAVAAAPAALPGPVTYFMERTDSGDYRLRVVPVGSNADADTATLSERGFVLDGLQGATRNTATLVLELPRDPVGTGDAWSLGTELILMEALGPQFQAGQPERSNRVKLASLTPADGGEQVATLEYDISEKLSGKVRGKDEPPTSPARAAEEDAEADDSGGPRPRATPETSASAEVSITGRGEFLVKAGRWRSWEGTVTSVTKGGFPTAALQVPTGALKLRLTAVESAPAPTAQPQQ
>NZ_CP017169.1|WP_174258685.1|1789036_1792582_+|DEAD/DEAH-box-helicase
MSEPPEKPVTPLFDTTRDALAWLRAQGLEHLSRLSLAVLMPLVEAAWLPQARPVLARRRLVELLSTDSLSRWMTEAMPSPRMKELLPTLAWRFVEAERLGAEASRASLEERLAPPAESRTHRVHGLLLALRARVPASVAPRPMHALVPDLMQYDAPLPGFRLRETRISELPVGAHAGFILPEARLIFAPTEVTGDCSCGATFCVHLLAAIDTALLWLRQPWSESFGEELEELVRPGWERALRALERAVDDSPGGPGGGEVSWRLDVINGYGVELAAYVHKRSKKGQRSTGAKVSRRKLLQDHGSQLSAADARLAALLPESEAPASRALLFELVGHPRIHLDENPDLLVRIERAKVGLVAEDRDGVVIVSAGVDGAMLPTAMLERLRKAQPEEGLYIWDDSQRVLTVLDAGPEVRALLTALNRHGNAFPPESHVALLDQLSKLSLRVPVALPRSVLGESVPLRYAPVVRMEAHASGAVRVELRTRPLPDSPTFIPGEGARDVHVRRGTGAVHAVRDFVQERDAAELLQARLPLDTAEPEELPFTFRFTSAQGGLAVLSACVELEPKPELEWVGAPVRLFHAAAPPALKVILERKRDWFGVLGGLSVEGERVELARLLDAARRKERFVQVDSTSYVEIEGALRQHLERLADHAHATRHGLEVGPSAVETLTALQDAGAEVEADKTWQSLVERIFAAKELKPRVSTGLKTELRDYQLEGFRWLTRLALWGAGGVLADDMGLGKTVQALTVLLDRSKRGPALVLAPTSVAFNWMDEAKRFAPSLRMTLFSDAADRGRTLEQLGPKDVLVLSYGLLTRDIERLSKLRFSTIIFDEAQTLKNATTHRFRAARALQGDFKFALSGTPLENHLGELWSLFAVVFSGLLGSWEAFRSRFAAPIERGVDPTAAPALARVLQPFLLRRTKAQVEAQLPPRTDIRVPIVLSSEEWALYEDARLAALSDLETRKPKMKEQERRIEILAALTRLRLLASHPRLYDAGSKLESAKLERFMELVRELRAEGHRALVFSQFTSHLALVREVLDAEGIDYEYLDGQTPAGARAERVRAFQEGDVPLFLISLKAGGFGLNLTAATTVIHLDPWWNPAVEDQASDRAHRIGQERPVTVYRLVTRGTIEEQMLSLHEHKRALVAGVLEGKDAAGRLSTQELLGLLSQRLAPPGEEEGPRTRH
>NZ_CP017169.1|WP_140788627.1|1793018_1793495_+|hypothetical-protein
MESSLGPASERNEKVKKRYRIDSVAQGFADEFLRASLPSQRAILVAACDAGLRNAGVVEPVASNALELIRSGSSGTDALRKDLDGLVAQYDEEYFSRSEEEGRVDLKAMVKFSKARAFAALSYALGEGDDWLEALYEAVSTMDEQKPIVERLRELLMA
>NZ_CP017169.1|WP_140788629.1|1793649_1794369_-|hypothetical-protein
MKFYVVEEDRSAGFTGNLRALPPWGFPGVTPCDACGAAGGWAGLQYPCVDLSGLQEREALENPGRQVSVEEFSRLRDLVRPFVPSWARLEPGADFGPPTGTGSGTFGDLFMQNPWSLYIRREALERLQDAGIHGLSGCPMNVRFRGKNPPELLAMQLELHGRLHIGGVPPEMRRVCPNCGMQRHELPQPPILDVHSMHEPPELFRLHDWPTFIVASERMADSVRRLPLTGVRFNELAAR

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Crispr_ID: NZ_CP017169_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_7

2303762-2303859

Orphan

Consensus_repeat	Method
CTCGGCCGGCCCCGAGACGGCGGGCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_7

>merge|NZ_CP017169|7|2303762-2303859|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGGATTCTTGTAGGGCGCTCCATAGGGGAGCTCCCGACGCCCACCGCCTCGGCCGGCCCCGAGACGGTGGGCGG

>NZ_CP017169|7|7|2303762-2303859|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGG	ATTCTTGTAGGGCGCTCCATAGGGGAGCTCCCGACGCCCACCGC
CTCGGCCGGCCCCGAGACGGTGGGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140789079.1\|2301652_2302507_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153249
NZ_CP017169.1\|WP_140853546.1\|2300572_2301511_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|200565
NZ_CP017169.1\|WP_140853541.1\|2287913_2289122_-\|DNA-polymerase-III-subunit-gamma/tau	unknown	unknown	gnl\|CDD\|237871
NZ_CP017169.1\|WP_140789085.1\|2308524_2310612_-\|RecQ-family-ATP-dependent-DNA-helicase	unknown	unknown	gnl\|CDD\|223588
NZ_CP017169.1\|WP_140800643.1\|2310658_2310910_-\|DUF3006-family-protein	unknown	unknown	gnl\|CDD\|378598
NZ_CP017169.1\|WP_140853549.1\|2313423_2314608_+\|PLP-dependent-transferase	unknown	unknown	gnl\|CDD\|99738
NZ_CP017169.1\|WP_140853550.1\|2314604_2315099_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	unknown	unknown	gnl\|CDD\|236483
NZ_CP017169.1\|WP_140853542.1\|2289159_2290737_+\|glycosyltransferase-family-39-protein	unknown	unknown	gnl\|CDD\|281842
NZ_CP017169.1\|WP_140797730.1\|2315317_2315569_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140853545.1\|2298457_2299771_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224153
NZ_CP017169.1\|WP_140789083.1\|2308127_2308511_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140797724.1\|2299844_2300555_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133022
NZ_CP017169.1\|WP_140789098.1\|2315578_2316133_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239516
NZ_CP017169.1\|WP_011552040.1\|2302542_2303466_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187551
NZ_CP017169.1\|WP_140853543.1\|2291116_2291581_-\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663
NZ_CP017169.1\|WP_140853548.1\|2310909_2311680_-\|DNA-repair-protein-RadC	unknown	unknown	gnl\|CDD\|178801
NZ_CP017169.1\|WP_140853544.1\|2293448_2298251_-\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP017169.1\|WP_140796396.1\|2292021_2293302_-\|serine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235461
NZ_CP017169.1\|WP_140797729.1\|2312368_2313331_+\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP017169.1\|WP_140789089.1\|2311837_2312296_-\|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|237999

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140789079.1\|2301652_2302507_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153249	cd07987, LPLAT_MGAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: MGAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this suubgroup are such LPLATs as 2-acylglycerol O-acyltransferase (MGAT), and similar proteins.	4.58442e-42
NZ_CP017169.1\|WP_140853546.1\|2300572_2301511_+\|polysaccharide-deacetylase-family-protein	gnl\|CDD\|200565	cd10940, CE4_PuuE_HpPgdA_like_1, Putative catalytic domain of uncharacterized bacterial polysaccharide deacetylases similar to bacterial PuuE allantoinases and Helicobacter pylori peptidoglycan deacetylase (HpPgdA). This family contains many uncharacterized bacterial polysaccharide deacetylases (DCAs) that show high sequence similarity to the catalytic domain of bacterial PuuE allantoinases and Helicobacter pylori peptidoglycan deacetylase (HpPgdA). PuuE allantoinase appears to be metal-independent and specifically catalyzes the hydrolysis of (S)-allantoin into allantoic acid. Different from PuuE allantoinase, HpPgdA has the ability to bind a metal ion at the active site and is responsible for a peptidoglycan modification that counteracts the host immune response. Both PuuE allantoinase and HpPgdA function as homotetramers. The monomer is composed of a 7-stranded barrel with detectable sequence similarity to the 6-stranded barrel NodB homology domain of DCA-like proteins in the CE4 superfamily, which removes N-linked or O-linked acetyl groups from cell wall polysaccharides. In contrast to typical NodB-like DCAs, PuuE allantoinase and HpPgdA do not exhibit a solvent-accessible polysaccharide binding groove and might only bind a small molecule at the active site.	3.68479e-121
NZ_CP017169.1\|WP_140853541.1\|2287913_2289122_-\|DNA-polymerase-III-subunit-gamma/tau	gnl\|CDD\|237871	PRK14965, PRK14965, DNA polymerase III subunits gamma and tau; Provisional.	0
NZ_CP017169.1\|WP_140789085.1\|2308524_2310612_-\|RecQ-family-ATP-dependent-DNA-helicase	gnl\|CDD\|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	9.44418e-156
NZ_CP017169.1\|WP_140800643.1\|2310658_2310910_-\|DUF3006-family-protein	gnl\|CDD\|378598	pfam11213, DUF3006, Protein of unknown function (DUF3006). This family of proteins has no known function.	0.000422016
NZ_CP017169.1\|WP_140853549.1\|2313423_2314608_+\|PLP-dependent-transferase	gnl\|CDD\|99738	cd00614, CGS_like, CGS_like: Cystathionine gamma-synthase is a PLP dependent enzyme and catalyzes the committed step of methionine biosynthesis. This pathway is unique to microorganisms and plants, rendering the enzyme an attractive target for the development of antimicrobials and herbicides. This subgroup also includes cystathionine gamma-lyases (CGL), O-acetylhomoserine sulfhydrylases and O-acetylhomoserine thiol lyases. CGL's are very similar to CGS's. Members of this group are widely distributed among all three forms of life.	2.88958e-134
NZ_CP017169.1\|WP_140853550.1\|2314604_2315099_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	gnl\|CDD\|236483	PRK09364, moaC, cyclic pyranopterin monophosphate synthase MoaC.	4.85408e-75
NZ_CP017169.1\|WP_140853542.1\|2289159_2290737_+\|glycosyltransferase-family-39-protein	gnl\|CDD\|281842	pfam03901, Glyco_transf_22, Alg9-like mannosyltransferase family. Members of this family are mannosyltransferase enzymes. At least some members are localized in endoplasmic reticulum and involved in GPI anchor biosynthesis.	7.33826e-20
NZ_CP017169.1\|WP_140853545.1\|2298457_2299771_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|224153	COG1232, HemY, Protoporphyrinogen oxidase [Coenzyme metabolism].	1.77158e-43
NZ_CP017169.1\|WP_140797724.1\|2299844_2300555_+\|glycosyltransferase	gnl\|CDD\|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. DPM1 is the catalytic subunit of eukaryotic dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. In higher eukaryotes,the enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	6.90707e-38
NZ_CP017169.1\|WP_140789098.1\|2315578_2316133_-\|NUDIX-domain-containing-protein	gnl\|CDD\|239516	cd03424, ADPRase_NUDT5, ADP-ribose pyrophosphatase (ADPRase) catalyzes the hydrolysis of ADP-ribose and a variety of additional ADP-sugar conjugates to AMP and ribose-5-phosphate. Like other members of the Nudix hydrolase superfamily, it requires a divalent cation, such as Mg2+, for its activity. It also contains a highly conserved 23-residue Nudix motif (GX5EX7REUXEEXGU, where U = I, L or V) which functions as a metal binding site/catalytic site. In addition to the Nudix motif, there are additional conserved amino acid residues, distal from the signature sequence, that correlate with substrate specificity. In humans, there are four distinct ADPRase activities, three putative cytosolic enzymes (ADPRase-I, -II, and -Mn) and a single mitochondrial enzyme (ADPRase-m). Human ADPRase-II is also referred to as NUDT5. It lacks the N-terminal target sequence unique to mitochondrial ADPRase. The different cytosolic types are distinguished by their specificities for substrate and specific requirement for metal ions. NUDT5 forms a homodimer.	7.1854e-42
NZ_CP017169.1\|WP_011552040.1\|2302542_2303466_+\|SDR-family-oxidoreductase	gnl\|CDD\|187551	cd05240, UDP_G4E_3_SDR_e, UDP-glucose 4 epimerase (G4E), subgroup 3, extended (e) SDRs. Members of this bacterial subgroup are identified as possible sugar epimerases, such as UDP-glucose 4 epimerase. However, while the NAD(P)-binding motif is fairly well conserved, not all members retain the canonical active site tetrad of the extended SDRs. UDP-glucose 4 epimerase (aka UDP-galactose-4-epimerase), is a homodimeric extended SDR. It catalyzes the NAD-dependent conversion of UDP-galactose to UDP-glucose, the final step in Leloir galactose synthesis. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.37601e-114
NZ_CP017169.1\|WP_140853543.1\|2291116_2291581_-\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	3.40448e-66
NZ_CP017169.1\|WP_140853548.1\|2310909_2311680_-\|DNA-repair-protein-RadC	gnl\|CDD\|178801	PRK00024, PRK00024, DNA repair protein RadC.	1.19364e-74
NZ_CP017169.1\|WP_140853544.1\|2293448_2298251_-\|zinc-ribbon-domain-containing-protein	gnl\|CDD\|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	1.00959e-40
NZ_CP017169.1\|WP_140796396.1\|2292021_2293302_-\|serine--tRNA-ligase	gnl\|CDD\|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP017169.1\|WP_140797729.1\|2312368_2313331_+\|thioredoxin-disulfide-reductase	gnl\|CDD\|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	1.73071e-151
NZ_CP017169.1\|WP_140789089.1\|2311837_2312296_-\|cyclic-nucleotide-binding-domain-containing-protein	gnl\|CDD\|237999	cd00038, CAP_ED, effector domain of the CAP family of transcription factors; members include CAP (or cAMP receptor protein (CRP)), which binds cAMP, FNR (fumarate and nitrate reduction), which uses an iron-sulfur cluster to sense oxygen) and CooA, a heme containing CO sensor. In all cases binding of the effector leads to conformational changes and the ability to activate transcription. Cyclic nucleotide-binding domain similar to CAP are also present in cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) and vertebrate cyclic nucleotide-gated ion-channels. Cyclic nucleotide-monophosphate binding domain; proteins that bind cyclic nucleotides (cAMP or cGMP) share a structural domain of about 120 residues; the best studied is the prokaryotic catabolite gene activator, CAP, where such a domain is known to be composed of three alpha-helices and a distinctive eight-stranded, antiparallel beta-barrel structure; three conserved glycine residues are thought to be essential for maintenance of the structural integrity of the beta-barrel; CooA is a homodimeric transcription factor that belongs to CAP family; cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) contain two tandem copies of the cyclic nucleotide-binding domain; cAPK's are composed of two different subunits, a catalytic chain and a regulatory chain, which contains both copies of the domain; cGPK's are single chain enzymes that include the two copies of the domain in their N-terminal section; also found in vertebrate cyclic nucleotide-gated ion-channels.	1.40745e-29

>NZ_CP017169.1|WP_011552040.1|2302542_2303466_+|SDR-family-oxidoreductase
MKPAVVVTGISGNLGRTLAKLLHKHERIIGIDRRPFAGRPKDVEMYELDLRKKKAEDVFRKNEIRAVIHMGIMHDPRMSEEEHHSFNVVGTTRLLEYCAKYGVKKVVVLSSANVYGPSPDNSNFLTEDAPLMAASRFSGVRDLIEVDMLAHSFFWKHPHIETVILRPVHIVGPTIKNAPSNYLRMRRPWMMAGFDPMVQLIHVEDVARAMVEALRPEPKGVYNVVGPGEVPLSAVMRELGNTPIPVPHPVARPLLGMLFKYRLANFPPPELDHIQFLCAVDGSRWVKDVAWKPRHSMRDTIRSVQGD
>NZ_CP017169.1|WP_140789079.1|2301652_2302507_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MLENVTDRVKKGLREWTDRLANNEQKQRLDGLARPGNEYGVDPFGFDLDYSLSAVAPLLWLYRNYFRVETFGIEHVPAGRVLLVSNHSGQLPMDGAMIGVAMMLDASPPRVIRSMVEKWVSSLPYVSTFMARVGQIVGTPENCRRLLESEEAILVFPEGTRGINKLWPQRYQLQEFGLGFMRLALETNTPIVPVAVIGAEEQAPALMDLKPVAKLLGFPSFPITPTGLPIPLPTKYRIYFGEPLHFSGRPDDEDSELDKKVRTVKASIQSMLHQGLKERQGVFW
>NZ_CP017169.1|WP_140853546.1|2300572_2301511_+|polysaccharide-deacetylase-family-protein
MRLASISVDLDSLPHYCRIHGLPESLLGARARSLVHAVAVPRFRELLDGLGIPGTFFVIGEDLESDPVAVAGMRASHEAGIEVASHSHAHDYALTRRGPEAIHADLARADAAILAATGARPEGFRAPGYTLNADLYAATAALGYRYGSSAFPAVPYYLAKAAVMGALSVLGRPSRSVLDTPRVLLAPRVPYRPDPAQPYRRGSGTVLELPMTVTPALRFPLIGTFATTLPRASLHALWRTCRRDTFFNFELHGVDVLDASDGIPPELVRQQRDLRVSATQKMARLREVFGWLKSEREVLTLRDVAGRLSASV
>NZ_CP017169.1|WP_140797724.1|2299844_2300555_+|glycosyltransferase
MAPHLTVVIPVYNEESIIASAAEELRQGLDARGLDYEIIFAENGSRDATPAILEELCANNSRLRWFHSETPNYGVALKAGILKARGTYVICDEIDLCDLTFYDAALPRLERGEADMVVGSKAAKGASDQRPLIRRAATRVHNKLLKVALGFQGTDTHGLKAFRREALLPVIQKCVVDMDVFASEFVIRAWREGLRVMEIPIQLHEKRQPSIHLFKRVPNVLKNVGKLFYVIRVRGT
>NZ_CP017169.1|WP_140853545.1|2298457_2299771_+|FAD-dependent-oxidoreductase
MEPIVILGAGLAGLSTAHFLNKPWRLIEKSDRVGGLIKTEVIQGCYFDPTGHWLHLRDPEIQALVNTLWLPEQMVRIQRKAGIFTRGVFTRFPYQVNTHGLPPEVVAENLTGYVEAVYGEKGRELREREPRNFEEFILRYMGEGFAKNFMVPYNQKLWTVHPREMSAAWVGRFVPRPNLKEVVDGALGAGSDAVGYNASFLYPREGGIESLARAMLSHLKGGQLSTHTEPTAIDWKARKVTLSDGSVQPYAGLVSSISLPGLVKLLAKGEAGVPDTVQDAAKQLRATTVTYVAVGAKGANRQPWHWIYLPEPEFHTYRIGSPSAVYAPLAPPDTSTFYVEYSHHGELSPAAAEKYAVEDLVRSQMIHAADDILFAQAREIPHAYVLYDDAYGPAKSEILRFLEHAGIQIAGRYGQWEYSSMEDAILAGRACARTLNG
>NZ_CP017169.1|WP_140853544.1|2293448_2298251_-|zinc-ribbon-domain-containing-protein
MKVSCPSCQTNYNIDDKRIPPGGAKLKCARCQTTFPIKLEAVSAPSAPAPAEPAQATAIPLPGATSAQSAAIPLPGAASAQAAAIPLPGAASAQSAAIPLPGAPASAQSAAIPLPGAPASPGAIPLPGAAPTHSAAIPLPGAPASTGAIPLPGAASAQAAAIPLPGAASAPSAAIPLPGAPEAFSAAPHAAAIPLPGAGAPQPTAIPLPGGAPEADPFAFDMGEPEQAAAIPLPGGAPEADPFAFDMSEPEQAASVPLPGSAPEADPFGFDMSEPEQAAMPLPGAAPEEDAFAFDMSSPAEAAAAMPQAGGPSDMDAFGDDFGEPVRDTREVTRVVSIPLPSDAYREPPAAPASGYGVNEPAGTARDFDFETVEAPVEDAAQGYGVNAPASTARDFDFADDALPVPVEAPPAEDAFAFDIESSSGAAQTQPPQEDPFALPPPAAYAQPAAPVDDPFALPPPDMAPQTDAFAPDVYAMPSAPEASPYAMPPPAAGAPSFDFGELPVPANADPFALPPPGADFSDLPAPAAPQALEFADLPAPAAPDLSFDFNEPPAPGADPFAVDFSAPPAPAADPFAADFGSAPAPGADPFAIDFSEPPAPAPAVAVNPAVDFGDVDFGAPSSPGIPDSLEFDPTARPDDDLEADLSDPLPPPPNAGPADGLEMLSFIDDAAGKDGGAQAGTKVRRFHVRRRSGKVFGPFDEGVIVKMLEDGQLLGNEDVSLDSETWSAIGTVPTFAAAIQRLMEGPAKLVTPTAAPAAAVIDAPRVDGASPQANMKRLEQLYEGRMAAVSVVDRSGNTEKWKKRVPLMIAAGVAVVVAGIGAGTEFGTRYGAFGRRALFPTRLSDGSAEAKQVADAKQALLTDTFDSYKQARELSAKVLAQKEYPEVRSLWCQSVYYLQRRYAAGNPNEMSRCRQDMADIEFLGEKDVDVIKASAAIALTSRQADSVIPTLSGAYGREDTQGDLELAFLLAEAYSQKRDEKRALDTLNKVLVKNPKSAKAHHAVGNLHQAADRADEAAAAYAAALEADPKHVASAVELAAVELLVRKDVAKGTEAVERALAEDVQSALGPAELARARGLKGVAMFQKHQPKEAEAELKAALEMDAKSTFLRGQLARVLRAQRNFEGALPIYKALATEEPNNLEFADGHITALVMTGKMQDALEAVKKANGVFPNEARIAYLYGRIEDALDNLSDAEGHYKRAIAADDNLVEARLYLGRFYLAQRRNAEARPQLEEAAKKAPENAGVRAGLGELALAENNTLLAQQEFERSVKLDPILADAHLGLSRVALLTDDLETAKAEANRALELDPHLLKDGRLQRGLVLWRLGQLEEAVAELEKAKTEDPRSTTIPITLGAVLLERGDLPGAESNLGLALSNEPSNHEALYYLALVKAKRLEFTQALDNMRKAVERAPNRPDYHYAYGVILRDAKNLPDAMSAWRKTVELDGTHADAHEALGHALLEGSQFDEAITSFEASLKADPRRTRVLGSIGDAYFAAARWNDAIKRYQSALKADPKLTYVYYKVARAFTEQAQHAKAIDWYRKATSLDSENPMAYYYLGFAYKERNKRREAVQAFKDYLSRKPDATDKKDIEDEIYDLQN
>NZ_CP017169.1|WP_140796396.1|2292021_2293302_-|serine--tRNA-ligase
MLDLRNVAQNFDAVVARLKTRGGNLDLGPFQRLFAERRELYVSVESLAARRNAANEEMKRKAKEDPKALDALRGDLRAVSQEIKEKEARLKDVEEELNRILLLIPNVPHESVPEGGGAEDNVQVSIWGQKPDLLFAPKQHFELGEKLGMLDFERAAKVSGSRFTFYKGALARLERALVTFMIDVHTSKGYTELLPPYLVLRETMMGTGQLPKFEDDAFKTLGEPERFLIPTAEVPVTNYHADEILEGESLPIRYCAFSPSFRAEAGAAGKDTRGLIRQHQFHKVELVKFAHQEKSLDELEAMTDDACDILRRLGLHHRVMLLCTGDMGFSARKTYDIEVWLPGQNSYREISSCSDCGDFQARRAKIRYRAQRGDKPQLAHTLNGSGLAVGRTTIAILENYQREDGSVAIPEALVPYMGGLKELKPI
>NZ_CP017169.1|WP_140853543.1|2291116_2291581_-|nucleoside-deaminase
MSDEAFMQQALSLARKAAELGEVPVGAVAVFNGEVVGAGFNRREVDRNPLAHAEMLAMDAAARKIGAWRLSGVTLYVTLEPCAMCAGGLVQSRVTRLVFGAFDPKAGAVGSLYNLVEEPRHNHRLQVTSGILADESRLLLKTFFGRLRAKKRDN
>NZ_CP017169.1|WP_140853542.1|2289159_2290737_+|glycosyltransferase-family-39-protein
MSLPSHEVGFHSPSGSAPGRADERFTPCVRERGREESAAPVSAPLLAAPTDSIPTPEPTSLAPGGTPQVAPVRNWMRWVLGAVALLPGLIAVVQLGRIHPDEVYQSLEPAWWRVHGYGVLAWEWRDGLRNWAVPGVLAGFLKLADLLGITHPRAYRVVVAIPQVALHAWSLWAAYRFAQRRAGTAGGLLSTLLVGLYGPLLVFAGRTMAESISASLLIVAVEALDRRERLARAGLVGGMALGLAVVARYPSAIFVLAALVWLAAARRWRLLAFTCAGGLGVAVALGALDWATWGSPFHSFFAYARFNVFSGKAAAQFGADAPSFYVKPLLTAVPLWAWAAVPVGIAALRQHRALSLPLWCAAVYTGVLLTTAHKEERFLYPGLVLGVLAAAPPVAAGLVQLARPAGPWGLAGLALVASMTAAAFFPSGDLRADQFRAIVAATRGNARGLLIVNEGLWGSGGFFYLGKQIPWLTCDWPHDGAFQRALRDRTFNRAVTFEDRALAELQAGGFQIVRKVGRETILSRE
>NZ_CP017169.1|WP_140853541.1|2287913_2289122_-|DNA-polymerase-III-subunit-gamma/tau
MSYLVLARKWRPQKFDDMTGQEHVVRTVANAIKMDRVAHAYLFCGPRGVGKTTAARLLAKALNCEKGPTAQPCGECRACTEIAAGTSVDVAEIDGASNNGVENVREIRENAKYLPQRDRHKIYIIDEVHMLSGAAFNALLKTLEEPPGHVKFIFATTEAHKLPDTILSRCQRHNFRRIPAARMLQRLQEICKAEGAGISDRSLSLVVRQSEGGMRDALSLLDQVLASCGANPSDEEVADALGAIDRTLVQDFADALVHKDAKRVLERVEEVFNRGLDLKRLAEELAFQLRHLFVTKTLGKAPDELAESEQKALMALAQNAEAAQLTRLFDVVHGCIWDVSRAAQPRLALEMALLKAIQLSPGGSIPELLARVDKLAAGMGEGSAKSNAGAPGGRSSPANFRA
>NZ_CP017169.1|WP_140789083.1|2308127_2308511_+|hypothetical-protein
MRYFSSRTDSPLLHIMWGNAFLLSLIYLLLGLGVEIALRYFPSRFLQRLSLSLDSLPARALELTGAMEPLRAAYFSGRISEVGVRVVFGITTMVVIFLLAMVVGTVMGGVRTLLARRALREGGRRHP
>NZ_CP017169.1|WP_140789085.1|2308524_2310612_-|RecQ-family-ATP-dependent-DNA-helicase
MMNMRAMPVDLPYLEEAQQGLVRHFGLSQFRPGQDQVISSVLSGRNTVVVMPTGAGKSLCYQLPATLLPGLTLVVSPLIALMKDQVEQLTARGIPATFINSSLSDLERAERMRKLRAREYKLLYVAPERFRSQSFLETVSALGVDLLAVDEAHCISQWGHDFRPDYALLGQVRKRLRPPRTVALTATATPEVRADIVRVLLMKDPQEFAMGFDRPNLFLGKQEVGGDADRHEACARLASTGGSGIVYCSTRRAAEDIFSELHGRGVKAVLYHAGMDDDARRRAQDTFMSAKEAVAVATNAFGMGIDKPDIRFVGHANIPRAVEAYYQEIGRAGRDGQAARAVLLFNHSDVFTQERLIQSSHPAEAIFGDVWNVLQSVEEFERGVHALAGTVNASEFEVSAALRILEREGKVERGGRGEGEHGITLLEKATSAQPHSPDAQRLLKSLLETFPVGRQVTTELPILARRIGLSVDEVRHALGLLEKAHVVKVRRPFAGRSIRALERVPFRELGLDLSRVREQERQNLSLLRRMTEYAYTDRDKKCRRSAILRYFGQRDTNTSCGNCDVCTPEKMPTLLAHGPAASRSRGTGSAAAPVVTNYSELASTELRRWRKELSKDLGVAPFIIFNDATLLGLSAALPVDREGFLAVKGTGESRWERFGPKVVEICLMARAAGHEPQAVPDAAVRARKPTIRRRS
>NZ_CP017169.1|WP_140800643.1|2310658_2310910_-|DUF3006-family-protein
MVSMVGLWGAVQVELLEDVRAQVVRLDTGQACTVERASLPTGVREGDVVVDGRLEPGQTEARRQDVARIRARLAVPVPPGFDL
>NZ_CP017169.1|WP_140853548.1|2310909_2311680_-|DNA-repair-protein-RadC
MEQAAAGAAWAGEGSVRARGVGGAEESRERLFRLGAAALTDPELLCLVWSSGPRAPGAWAVAGALLSEGGGLKGLVQQEPLALSLRPGVGPVRAAQALAALELGRRSQRARERRPRLRTPKEIAAYLAPVLGALRREVFHVLCFNARNVLVHDARVAEGTMNTCPVDPREVFAAALTSRATSIVLAHNHPSGDPEPSVQDLGLTRHLVAGAQLLNIKVLDHVVMGDGGYVSMLERGLMPDEAQEKRRAWSANGGGG
>NZ_CP017169.1|WP_140789089.1|2311837_2312296_-|cyclic-nucleotide-binding-domain-containing-protein
MDAAVLKKVALFEGLTQGQLAKVAQIGHSRTYPAGAFLFREGETGQEMFVIAEGKVRISKSVPGIGEEALAILEPGQYFGEMAVIEDSPRSADAIAHVSCAVWVIERSRLDQLMFTDKDLAYVLLWTFVRTLSERLRETNEKIKGFFALSRF
>NZ_CP017169.1|WP_140797729.1|2312368_2313331_+|thioredoxin-disulfide-reductase
MVEEKINKVTIIGSGPAGYTAAIYAARANLQPVVFAGGPTLEHPQRVPGGQLMVTTDVENYPGFPEAITGPELMERFQKQAERFGTTIHMENVVKVDFSQRPFLIQGESVSCRSETVIISTGATAKWLGVKGEDTYKNRGVSACATCDGAFFKKQDVLVVGGGDTAMEEATYLAKIVNHVTLIHRRDTLRASKVMQERARQNPKISFMWDSAVEEVLGDAKGMNGAVVRNLKTGDSHQVKATGLFVAIGHTPNTELFQGVLETHQGGYLKTVPGSTRTNIEGVFACGDVQDHYYRQAITAAGTGCMAAIDAERWLIEHGE
>NZ_CP017169.1|WP_140853549.1|2313423_2314608_+|PLP-dependent-transferase
MSSKQKTVAVHAGTRLAGSKAVPVSPPIYPAAVNWFDSSDDLDSALDGKDYAYARISAPNTTLLEEAVAALEGAEACVAYASGMAALRSVFEAQGFRAGDTLVMPADGYGVTRALYKSLCATLGVELHAFLMTDPEVPGRIRELKPRMVLAESISNPLLRVPDLRVLARACQDVGATFVVDGTFPSPVGQRALALGADYAVQSTSKWLNGHSDALGGTVSASLERMAPLRAARVLAGDVLGPFEAWLTLRGLRTLPVRMKAHVEHAAHVARRLAESPLLERVIYPGLASHPDHATAQELLLGGGPMVAFEIKGAGRPECMRFLEALKVGRPGPSLGDVCTLVMHAASASARRFTPEEREAAGIRENLIRVSVGLEDPDDIVDDLLAAVAQGVRR
>NZ_CP017169.1|WP_140853550.1|2314604_2315099_+|cyclic-pyranopterin-monophosphate-synthase-MoaC
MKMVDVGGKPKTGRVAVATALLRMLPDTRERILAGKVEKGDVLAAARLAGIMAAKRTPDFVPLCHPIALSGVEVTLAPEDAGLRVRVQVKTVDRTGVEMEALTAACAAALTVYDMCKSVDRGMVLDAVQLEHKSGGRSGTWRREDATPAEAAAPRRRTRAKKAR
>NZ_CP017169.1|WP_140797730.1|2315317_2315569_+|hypothetical-protein
MFDLRGVLTLLTALGAAGCGALTEEGDAADVSQPVADRAACDAQAAQRRYVSEDRKECQVVFFVCARGESPFFDACGCGCSRP
>NZ_CP017169.1|WP_140789098.1|2315578_2316133_-|NUDIX-domain-containing-protein
MAREVKPWRRLRRGLEHDFSVARVREDWWADPRTGHEHPRVRVDCADWVNVIAVTPDAQLVLVRQFRFGVEASTLELPGGIVEPGEAPERAAARELEEETGYVPGRMVPVGQVHPNPAFQGNVCFNFLALDCVKRHEGRQDAGEDIAVELHPRADLPRLILEGHISHSLVVAAFFQERLLSESK

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Crispr_ID: NZ_CP017169_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_8

3469765-3469989

Orphan

Consensus_repeat	Method
GGCGGGTGCTCCGGTGCC	CRT

4 spacers

The CRISPR arrays of NZ_CP017169_8

>merge|NZ_CP017169|8|3469765-3469989|CRT
GGCGGGTGCTCCGGTGCCACCAGGGCTGATGGGAGCACCGCCTCCGGCGGCGGGTGCTCCGGTGCCTTCGGGGATCATGGGCGCAAATCCTCCTGCGAAGGTTGGAGCGGGTGCTCCGGGGCTGATGGGCGGGCAGGCTCCTGCGACGGCTGGGGCGGGTGCTCCGGTGCCTCCGGGAATGACGGGGCATCGGCCTCCGTCCGCGACGGGGCTGCCTGCGGTGTC

>NZ_CP017169|8|1|3469765-3469989|CRT
GGCGGGTGCTCCGGTGCC	ACCAGGGCTGATGGGAGCACCGCCTCCGGC
GGCGGGTGCTCCGGTGCC	TTCGGGGATCATGGGCGCAAATCCTCCTGCGAAGGTTGG
AGCGGGTGCTCCGGGGCT	GATGGGCGGGCAGGCTCCTGCGACGGCTGG
GGCGGGTGCTCCGGTGCC	TCCGGGAATGACGGGGCATCGGCCTCCGTCCGCGAC
GGGGCTGCCTGCGGTGTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140854274.1\|3484615_3485896_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017169.1\|WP_140854266.1\|3478576_3480376_+\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|119365
NZ_CP017169.1\|WP_140798155.1\|3463023_3464169_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340833
NZ_CP017169.1\|WP_140798152.1\|3459364_3460480_+\|LptF/LptG-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP017169.1\|WP_140798149.1\|3452606_3454151_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl\|CDD\|234854
NZ_CP017169.1\|WP_140798151.1\|3456993_3458259_+\|phosphoribosylamine--glycine-ligase	unknown	unknown	gnl\|CDD\|234856
NZ_CP017169.1\|WP_140854276.1\|3486221_3487529_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017169.1\|WP_140790535.1\|3464387_3465782_+\|undecaprenyl-phosphate-glucose-phosphotransferase	unknown	unknown	gnl\|CDD\|274396
NZ_CP017169.1\|WP_140854270.1\|3482306_3483179_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017169.1\|WP_140796455.1\|3481815_3482310_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP017169.1\|WP_140854259.1\|3461803_3462967_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340838
NZ_CP017169.1\|WP_140854279.1\|3488091_3489411_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017169.1\|WP_140854272.1\|3483175_3484408_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140790526.1\|3458255_3459368_+\|LptF/LptG-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP017169.1\|WP_140790542.1\|3478079_3478421_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP017169.1\|WP_140854262.1\|3465850_3467788_-\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP017169.1\|WP_140798153.1\|3460481_3461807_+\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP017169.1\|WP_140790541.1\|3474682_3477475_-\|vitamin-B12-dependent-ribonucleotide-reductase	unknown	unknown	gnl\|CDD\|235828
NZ_CP017169.1\|WP_140854268.1\|3480472_3481672_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140854256.1\|3454154_3456992_+\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140854274.1\|3484615_3485896_+\|hypothetical-protein	gnl\|CDD\|275097	TIGR04275, beta_prop_Msarc, beta propeller repeat, Methanosarcina surface protein type. This model describes a repeat region found mostly in cell surface proteins of various methanogens. Methanosarcina barkeri, for example, has twenty such proteins, often with either seven or fourteen repeats. These repeats resemble the beta propeller repeats of the TolB periplasmic protein of Gram-negative bacteria, part of a complex associated with various functions including biopolymer transport (see TIGR02800).	0.000202989
NZ_CP017169.1\|WP_140854266.1\|3478576_3480376_+\|glycosyl-hydrolase	gnl\|CDD\|119365	cd06548, GH18_chitinase, The GH18 (glycosyl hydrolases, family 18) type II chitinases hydrolyze chitin, an abundant polymer of N-acetylglucosamine and have been identified in bacteria, fungi, insects, plants, viruses, and protozoan parasites. The structure of this domain is an eight-stranded alpha/beta barrel with a pronounced active-site cleft at the C-terminal end of the beta-barrel.	4.98793e-141
NZ_CP017169.1\|WP_140798155.1\|3463023_3464169_+\|glycosyltransferase	gnl\|CDD\|340833	cd03804, GT4_WbaZ-like, mannosyltransferase WbaZ and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. WbaZ in Salmonella enterica has been shown to possess mannosyltransferase activity.	8.16056e-147
NZ_CP017169.1\|WP_140798152.1\|3459364_3460480_+\|LptF/LptG-family-permease	gnl\|CDD\|367632	pfam03739, YjgP_YjgQ, Predicted permease YjgP/YjgQ family. Members of this family are predicted integral membrane proteins of unknown function. They are about 350 amino acids long and contain about 6 transmembrane regions. They are predicted to be permeases although there is no verification of this.	1.25206e-65
NZ_CP017169.1\|WP_140798149.1\|3452606_3454151_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl\|CDD\|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0
NZ_CP017169.1\|WP_140798151.1\|3456993_3458259_+\|phosphoribosylamine--glycine-ligase	gnl\|CDD\|234856	PRK00885, PRK00885, phosphoribosylamine--glycine ligase; Provisional.	0
NZ_CP017169.1\|WP_140854276.1\|3486221_3487529_+\|hypothetical-protein	gnl\|CDD\|275097	TIGR04275, beta_prop_Msarc, beta propeller repeat, Methanosarcina surface protein type. This model describes a repeat region found mostly in cell surface proteins of various methanogens. Methanosarcina barkeri, for example, has twenty such proteins, often with either seven or fourteen repeats. These repeats resemble the beta propeller repeats of the TolB periplasmic protein of Gram-negative bacteria, part of a complex associated with various functions including biopolymer transport (see TIGR02800).	0.000136821
NZ_CP017169.1\|WP_140790535.1\|3464387_3465782_+\|undecaprenyl-phosphate-glucose-phosphotransferase	gnl\|CDD\|274396	TIGR03023, Sugar_transferase., Undecaprenyl-phosphate glucose phosphotransferase. This family of proteins encompasses the E. coli WcaJ protein involved in colanic acid biosynthesis, the Methylobacillus EpsB protein involved in methanolan biosynthesis, as well as the GumD protein involved in the biosynthesis of xanthan. All of these are closely related to the well-characterized WbaP (formerly RfbP) protein, which is the first enzyme in O-antigen biosynthesis in Salmonella typhimurium. The enzyme transfers galactose from UDP-galactose (NOTE: not glucose) to a polyprenyl carrier (utilizing the highly conserved C-terminal sugar transferase domain, pfam02397) a reaction which takes place at the cytoplasmic face of the inner membrane. The N-terminal hydrophobic domain is then believed to facilitate the "flippase" function of transferring the liposaccharide unit from the cytoplasmic face to the periplasmic face of the inner membrane. Most of these genes are found within large operons dedicated to the production of complex exopolysaccharides such as the enterobacterial O-antigen. Colanic acid biosynthesis utilizes a glucose-undecaprenyl carrier, knockout of EpsB abolishes incorporation of UDP-glucose into the lipid phase, and the C-terminal portion of GumD has been shown to be responsible for the glucosyl-1-transferase activity.	0
NZ_CP017169.1\|WP_140854270.1\|3482306_3483179_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	3.07061e-05
NZ_CP017169.1\|WP_140796455.1\|3481815_3482310_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	1.16944e-26
NZ_CP017169.1\|WP_140854259.1\|3461803_3462967_-\|glycosyltransferase	gnl\|CDD\|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	5.46246e-81
NZ_CP017169.1\|WP_140854279.1\|3488091_3489411_+\|hypothetical-protein	gnl\|CDD\|275097	TIGR04275, beta_prop_Msarc, beta propeller repeat, Methanosarcina surface protein type. This model describes a repeat region found mostly in cell surface proteins of various methanogens. Methanosarcina barkeri, for example, has twenty such proteins, often with either seven or fourteen repeats. These repeats resemble the beta propeller repeats of the TolB periplasmic protein of Gram-negative bacteria, part of a complex associated with various functions including biopolymer transport (see TIGR02800).	0.000120605
NZ_CP017169.1\|WP_140790526.1\|3458255_3459368_+\|LptF/LptG-family-permease	gnl\|CDD\|367632	pfam03739, YjgP_YjgQ, Predicted permease YjgP/YjgQ family. Members of this family are predicted integral membrane proteins of unknown function. They are about 350 amino acids long and contain about 6 transmembrane regions. They are predicted to be permeases although there is no verification of this.	1.79239e-80
NZ_CP017169.1\|WP_140790542.1\|3478079_3478421_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl\|CDD\|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	5.71823e-22
NZ_CP017169.1\|WP_140854262.1\|3465850_3467788_-\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	1.98617e-16
NZ_CP017169.1\|WP_140798153.1\|3460481_3461807_+\|O-antigen-ligase-family-protein	gnl\|CDD\|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	7.1369e-10
NZ_CP017169.1\|WP_140790541.1\|3474682_3477475_-\|vitamin-B12-dependent-ribonucleotide-reductase	gnl\|CDD\|235828	PRK06556, PRK06556, vitamin B12-dependent ribonucleotide reductase; Validated.	0
NZ_CP017169.1\|WP_140854256.1\|3454154_3456992_+\|zinc-ribbon-domain-containing-protein	gnl\|CDD\|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	1.71171e-20

>NZ_CP017169.1|WP_140854262.1|3465850_3467788_-|trypsin-like-peptidase-domain-containing-protein
MKRIPLACLVTALATGAPAALASDEVCQQEEVSSSSQRLTKVGEDVFRRFETTHPYATTQIRASDGPIHTDVITHAGAAYIAPHFERLDLEDGDFVVVRAPDNSRSWRYDNSHPGARSGFWAIHIAGETAIIELHSRDSVNRRGILNKHGYSIDRYARGYTNEEMGLSNDKALCGPDDTQWAPCYASSDPTLYGRARPVARLLINGSGACTGWLVGSQGHLMTNQHCVGTASEAQNTHYEFMAEGASCSTSCASWFGCPGNVIPGGTLVKVDAPRDYALIQLSQNPVNTYGYLQLRSSGAVVNERIYLPQHPAGHGKKIAVRSTDARDESGFAEIYSRNEASCQSGGPNDIGYYADTQGGSSGSPVIGHSDNLVVALHHCANCPNRGVPIEAVISHLGTSLPQCALPAADCPNPGGNGEPPPPPPPPPPPPENSFDYSASNTNSAQQNTTNHTIALTAGQTLTVATCGLTGTQFTGDTWLRLRNPAGTEVATNDDSCGGRGSSITFTAATAGNHEVLAGCYSSGSCTGRVVWEITGGSGSPTSGSFNFSGSNTNSAQQNTTNRDVAIAAGKSITVATCGVTGATFTGDTYLRLFNGTTQAAVNDDSCGGTGSSLTYTSPTATTLQIRAGCYSSGNCTGTVVWNIQ
>NZ_CP017169.1|WP_140790535.1|3464387_3465782_+|undecaprenyl-phosphate-glucose-phosphotransferase
MFSRLQRFYTSIKVVADMVMLALAFVLAYATRFSGIVPVTEGIPPWTDSFFSLLMVLVIFPVTFHQSRLYGTNRSRTNTGEVFEVFKSTITAALILVAVTYFVRERYSRLTLVIFIVYAFALVTCSRLVTRYLVSEIRRRGHNLKSILVIGAGDLGQRVIETVEHHRELGFRVMGVLTLHPEKVGQYVNDVRVIGLVDQVNEVLDSHPVDQVILALPLEGHAHVKALMDKLALRTVDVRVVPDLYQYITLYGGLEEFGGLPIIRLQGDPMEGWSRVAKRAFDILFSLLAILITAPLMAATALAVRLTSRGPMLYRQERMGMDGRTFPILKFRTMRIDAEHSGAMMACPDDPRRTVIGTFLRKYSLDELPQFFNVLRGDMSLVGPRPERPVFIEEFKRQIPRYHLRHKVKAGITGWAQINGLRGQTCIEKRIEYDLYYIENWSLLMDLKILVRTALGGFLSKNAY
>NZ_CP017169.1|WP_140798155.1|3463023_3464169_+|glycosyltransferase
MKVALVHDWLVTHRGGERVLDALCEVLPDADIYTLIHKPGSQSPAIESRRIFTSFLQHIPGIHARYRHFLPLMPKAIESLQLQGKYDLVLSSSHCVAKGLRTPRGTPHLSYVHAPMRYMWDLFDDYFGPGRTGLPVRAAAHAIRPWLRRWDRRTAAGVDRFIANSRHIATKVQRFWGREASVIHPPVSLERFAQVPLEGGGQGGYFLWLGAFAPYKRLDVALEAFRNLDAQLWVVGTGQEAARLGAGSLPENIRFLGNVLDASLPALYRDARALIFTPEEDFGITPLESQAAGRPVIAYGKGGALETVTAQTGMFFSEQTPESLAAAVRRFDEWEAGFRPEAARAQAERFGRAHFQSAILREIHSVLGDVLPDSPGPAAGL
>NZ_CP017169.1|WP_140854259.1|3461803_3462967_-|glycosyltransferase
MPARPPWRPRVWYAEAVAHVLLDLRMVRGRLHGIARYALELARRMPVLAPDLRFSALVPPEGLAPDLGELTPRMPLHRALAGFLSPLEQPALAADLVKLAPDAFHATSFSLPLFWNGRLVATLHDANHLALADQYTPAQSIYYRVVVGPRAKRATALVTVSEFSRDELAKHLKLSPYRLQVIHNGVDARFQPPTQAEAAAFRERYELPARYVAAVGNAKRFKNLALLKDFAGELPVPVVLLAGKGAVAHELGLHENVFDLEELPEDQMPLFYGAASALLLPSRYEGFGLPALEAMGAGCPVLASDATALPEVVGNAALRLFPDDAAAWREATLRVLRDDVLRRELVELGRERVARFTWDDCARRTLAVYRRVLEAPAPGGSRGTHPR
>NZ_CP017169.1|WP_140798153.1|3460481_3461807_+|O-antigen-ligase-family-protein
MSAHMGTASELPLDLRWRRAINAVLVLWTVGLVLAEVVLQVATGAAVLLAAILLVRGRLRLAPDVRAYVGASGVLCLWQAASPAVALLTGAAESWPRGSRYGQVLDSVAGAAAACIGAVGVPWLLLAGVLAGGWLLAALLGVFQNRVRWSMELPSFLKLNLGRLHENFGTEESPRYAAGGFFSHRLRFAHGAIAALGPALSVLGIADQARRRVLAGAVVMGMLISIYNAFARAALGAALLVSVVALLLLVQGSARKMGLALLFALVAVVSMSPAWRTRLEKAVGNIYGGEREHAMAVGWSLVREYPLTGVGFGNHKPAALATQDETGITDLLATDSHNLWLTVWAETGLVGLLLTLAMHALLGRALIRRYREGSIAATGALLSWVGFHILALVHYLPFHSSVYLSFSLIWGLGLCEGSERLRGREARQGLLEVEGAPRPSP
>NZ_CP017169.1|WP_140798152.1|3459364_3460480_+|LptF/LptG-family-permease
MRGTLFIYVLRTYLRFALGILGGLVLVFVVVDFVDRAKLYTGPGWVWDVAELYFYKAMMSVQQLGPAALLLAAGTTVSALRKQGEVTAIRALTFGPSALYLPILVASFVACVGLVAFDERVATYSGRRVDEITTQRFNKWGDWRFYYTPKQWFRRGDNIFFLRGGSAQEGFQDVSVFTVTESFDLQRRLDASGMFPVEGMRWRLTDVVERTFDGEGKTSVRQLPEAEYELGVAVTAFRIRPGRPEQMRASELREQIVARRDVGLATKQFELALHNRFAYPMAAFPAALLGVGLALRTNRRGHLTAAIIEGLLTAVAMWGLMMVCRTLVLTERLSPGVAAWTPTVLLGLIAGAVWLQREGRLHLPRRSLLVR
>NZ_CP017169.1|WP_140790526.1|3458255_3459368_+|LptF/LptG-family-permease
MNRLSRYLLGELLVPLGVWVAFMFLLLFVMQFLRGTDVLLGSSVTLVDMARLLAYLAPHFLMMALPIAFLLAILLGLGRLGEDRELVALQALGIGPVRLLAAPMGIAVALSVLMLVITSTAQPWGLAGLKVLVSEVIRKNAVGDVKSGVFYEDLSNLTLYAEQVSADGKWTNVLLHDDREANSPLLVLAQRGQVGTSTSGEVLRFALEAGEVHRSAGRETEEYSIIRFDQAEISVGVGASMGKRSRFSFSREELTPGELLEAAREAEAQGEDARMYRMALHSRLGNALAPIAFALLGTPLAMGRRQSGRAWGYLLTLGGYVLYYLLSRVFEQMGQKGQLPVGLAGQMANLVFVAVGLVALYRVSRSGTVK
>NZ_CP017169.1|WP_140798151.1|3456993_3458259_+|phosphoribosylamine--glycine-ligase
MDVKVLLLGSGGREHALAWKLSQSPLLTQLLCGPGNPGTAKLGTNVALRADVPEEVAAFAKREAVDLVVVGPEAPLVAGVADALADAGIACFGPVAEGARIEGSKAFAKEIMAEAGVPTAAFQTFTDVAAAEAYAVEQGRIVVKADGLAAGKGVIVAHDVEAARAAVRAVGAMGAAGQTMVLEELLEGEEVSAMALCDGERYAMLPLSQDHKRVGEGDTGPNTGGMGAYSPAPFLSAAQLAEVGERVVAPTLAVLRRRGIPFRGVLYAGLMLTRGGPKVLEFNARFGDPETQVLMMQLGEDLLPLLDACARGTLTPRTLVSSPGASVGVVLAARGYPDAPEKGQRIEGLDAVPPDATVFLAGVEARDGGVVTAGGRVLTVCARGEDLAQARERAYAAAAAVRFEGMHFRRDIGARGMKAAP
>NZ_CP017169.1|WP_140854256.1|3454154_3456992_+|zinc-ribbon-domain-containing-protein
MRIVCQKCAAAYAIDDKLITAKGVRAQCPRCRNLQLVRRDPSAVPAAGAPAPASQPAAPVTLTPVSGAAPADDLFGDFGAPPPAAPAPGAAPAPKPARGERAPGSELFGDFGAMPSPAPASAPPVDPFAGLGTPASGGGGAGAEDPLLDFLGPPPSAPQGMESQPSRPAKPAAAKPATSGCRVCQKPLTDSFDQALGICDGCRQPGSAQAPAAASRPAAPAGNSDFLPAMADLGGGSASVAQASEPEPGAESRSGARVPISTDIIPDMGPEPRSGIRASSPQLGAEPRSGSRSAPVRVTDGRSRGGKGGLVAGLVGLVVVGGGVGGYFLYQQQQEASRRQAGPPPAAAIPDAVQAVLPRWKLKYLEIPGTSAERLAQGQQQLARDERFAYAEAEESFQQALVLDPTSDAAIAGYVQALALGRGARMDDVTFQEARALLSAAESRSGRTAPLLLAHANLLLARSGQPEQARPLAEELLARAELPDAQKAEAHLVLGRTWLSSSRELARSHFDSAQKLSPDIKRLHYYRALAHVSGGEYSAALDTLRKRLETSPKDWESLALTARIYQEVGEPAEARKLYEARVKAEPGELRALLPLAMLRYQAEGNAAGAVRDLRALMKNRARYDEPEVAEVLVHLAAAERTAGSQDAAVKSAEEALQLVKELPEAHLQLFLVGLSRRDAEKARTHLAGFRGQLEDGALEKVLEGRLLLLEKKPLDALEAFQEAVKLDARRLDAQLLAGVAAASAKRRDDAFRALHQALQSDPLRLEPRPATSAYWLRPRETVEGVEGAILALSEGPEDPSPLLYEGLLRFHQHQFDAAERHLRSVLEVDANNAGALAYRALIALQRGATADARRLGERSAAAGRQMPVSHLAHGLALAEARQVEPAKRALRDALALAPTLLSAQARLAQLESARGKDVARDTLVKVVGLDPAYLPAKRMLYLLER
>NZ_CP017169.1|WP_140798149.1|3452606_3454151_+|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MLALLSVSDKRGLVPFAQGLVRLGFRLLSTGGTLEALKGAGVPVTKVSEHTQSPEILGGRVKTLHPRIHGGILGRLELEADREEMKAHGIEPISLVAVNLYPFRQTVASGAAEPEVIEQIDIGGPAMVRASAKNFRHVSVVVDPDDYPAVLAELEQQKAVSEDTRRRLMRKAFAHTAAYDASISAWLSAQAGEPFPGELSLAFRKSQELRYGENPHQRGAFYREHAAPQEPTVAFAKVLQGKELSYNNILDLDAALGLLLEFPEAPAAVIIKHNTPCGVAVDDALVKAYRTARAVDEVSAFGGIVALNREVDAATAQAMAETFLEAVIAPSYSPEALQVLAAKKNLRLLEAGPALASPQARPRAQLDARSVSGGMLLMDRDSVEPPLSWKVVSKRVPTPEEERAMRFAWKVCKHVKSNAIVFASGDQLLAQGGGQTNRVDSVRIAMQRGGAALRGSAVASDAFFPFRDGLDEAARAGATCVVQPGGSVRDAELIAAADEHGMAMVLTGVRHFRH
>NZ_CP017169.1|WP_140790541.1|3474682_3477475_-|vitamin-B12-dependent-ribonucleotide-reductase
MDKELSSKSTVNGKERRGGRKARVAATGLTVERFFTTPGVDPADELAWEYRSASITGEDGKAVFEQKNIEVPKSWSMLATNVVASKYFRGTPGTPERETSVRKLVARVVDTLTRWGVEGGYFTRDADREAFHAELTHLLLRQKASFNSPVWFNVGVEAQPQCSACFINSVEDNMDSILTLARTEGMLFKYGSGTGSNLSTIRGSKELLAGGGTASGPVSFMRGFDAFAGVIKSGGKTRRAAKMVILNAEHPDILEFIRCKSTEEKKAWALIEAGYDPSFNGEAYSSVFFQNSNNSVRVTDAFMKAVVDDATWTTRSVRDGQPLDTYQARELFREISEAAHLCGDPGMQFDTTVNSWHTCSTTARINASNPCSEYMFLDDSACNLASLNLMHFRTIDGDFDVTAFRHAVDILLMAQEIIVGNSRYPTERIEKNSHDYRPLGLGYANLGALLMASGLPYDSPAGRNYAGAITSLMCGEAYAMSARLAEKQGPFAGYAKNAEPMLGVIRKHRKAAYHIAPEGVSQGLFAAQKDAWDRALALGEEHGFRNSQVTVLAPTGTIGFMMDCDTTGIEPDIALIKYKKLVGGGMLKIVNQTVPLALEKLGYPQTQSQDIISYLDKQDTIEGAPHLKPEHLPVFDCAFKPAQGERSIHWMGHIQMMEACQPFLSGAISKTVNMPSDATVEDIEKAYLEAWKRGLKAIAVYRDGCKRTQPLNTSKETVKDTRAAKSTVAPEPAPAVQPEPRAVRRRLPDERRSITHKFSIGGHEGYLTVGMYEDGLPGELFIVMAKEGSVVSGLMDSFATSVSLALQYGVPLKVLVDKLSHTRFEPSGFTGNPDIPIAKSITDYIFRWLELKFLPSEEEDAVLDRVDVQPKREALPAQTASVQRSDSNSSKRSTWLNQADAPPCHTCGAIMVRSGACYKCGNCGATSGCS
>NZ_CP017169.1|WP_140790542.1|3478079_3478421_+|(2Fe-2S)-ferredoxin-domain-containing-protein
MAPPYQRHVFVCTNRRPDGNPKGCCASKGAEEVRAAFKAELDKRGLKGHMRANAAGCLDTCSFGVAVVVYPEGTWYGGVQVEDVKDIVEQHLMEGRPVERLLMPFSRKAVTPG
>NZ_CP017169.1|WP_140854266.1|3478576_3480376_+|glycosyl-hydrolase
MRRSWWASGLIATALSVAGCDSEVSSSHVRDLMAFQDAALAAEWSVGVAYSVGTRVTYQGRLYECRQPHTSQADWTPVAVAALWLDLGPAGGGEPDAGSGGTDAGTGGDVTAPTVGLSASTSRIIAAGPLSLTATATDDVGVTRVEILENGTVVATGSQFSRAFSGWEQNGTYVYAVRAHDAAGNVGTTTLTVVVDIPGGPPPGGKRIVGYFTAWGIYARNYHVSNVQPSKLTHINYAFSNISGDGRCILGDPFADIDKGGGWQGEWDPGQLRGNFRAFKEMKRQNPHLKLLISVGGWSWSTHFSTVASSPASRAAFVKSCVDLYIRGQYPGVDPVNGEGVFDGIDIDWEYPVGGGLPGNSNSPADKQNYTLLMQEFRSQLNAVTTQTGKPYLLTIATGASPDLLENKQETKKLSDVLDWINVMSYDYHGAFESTVNFHSALNRVTGDPGAATGFYTDGSVSKMLALGVPPAKIVVGVPFYGRGWGSVPNVNNGLFQSGVPTRGTWDDGSSGLTGVFDFKDIKANYERAGSGYTKFFHPEAKQAYVYNPATGIWIGYDDVQSMNAKADYILNKNLGGAMFWELSGDDGSLLDALARKLR
>NZ_CP017169.1|WP_140854268.1|3480472_3481672_+|hypothetical-protein
MSFAAAVLLVALSSSSVAAEPWTAVVRVASDEDTALLVRVRGQSSDLPMRLEVSSGAPLEGFREGPWLAAERLAGHHQARAVLWFVREGSDVRVQVAEFDSRRLFSRAARLGQSPGSLEWSTGAEALALAARSALRAVEAGAPLGDVVEVAPPRHASNEEGSETGVGRRIGEAASGDEAAPRTPTSPSPEEAIALAEDGALASARECVASPREGLGLASAEENPARQMWLALGGHAALDGYTRRGHQGLVVGVGLQPGRWRLRAQVLASVPTRLRDARTELTLGQHAASVWAGLPWAAAEGLDVEAGFGAGAVVFTRRTQALTEDVKAAPPGTMLALLMGPELRTRWRMGARVGLETSLAAEVLLGRPELRYAIDGNFVSRGAGWAVRPRLGLAMVVFL
>NZ_CP017169.1|WP_140796455.1|3481815_3482310_+|sigma-70-family-RNA-polymerase-sigma-factor
MLMELLPRVRNLVRYLVRGDVDVEDIAQEALIALVRGLPSYRAEGRFQSWADRVVARTAFAWLKRSRGRDAQHADAPVELVAVPSEDALPDEYVHRRHMVTLLDRLSTEQRHALVLHHVLELSVPEISTELGIPFETVRSRLRLGRTALRSLASAEGDGGEERG
>NZ_CP017169.1|WP_140854270.1|3482306_3483179_+|tetratricopeptide-repeat-protein
MSDFREEGDDALNALVLPLDEGAGPARRISRERSAQMVLAALEAGALVSQPTPRPRGKRPPVWLMTGALLVAGAAAAAVWSFTRSSRASTSQVEEAVLTSPPRLGTASQWSDTEAVDAAPSRLDAVSEVVPAETPAVPAAFIAEAEGASEPARPRAPPATVKSAAPEDLLLKANGLRSDGRWKEAEALYLRVIRAEPSSLASYVARVASGSLRLEHLGDARGALRQFKAALRIQPRGVLDQEAQHGIAEAHRVLGNRVAERSALESFLSTHPDSPLVPSARARVRELTAP
>NZ_CP017169.1|WP_140854272.1|3483175_3484408_+|hypothetical-protein
MNRRWTLAVLLAASMGSCTRGDLVATVQSPDAGHVGSSADAGGPDGGEPPDDWEAYCAGRGPPIVVGDAYTDSQVCSGRLAERTFRHALCTCEGLALGASFETDAFHGTTGTYQPGGAGGDVGVNGALSANDAVSVGGSLSIGGAGGAQLGQTFRVGDALHCGGPLTGNPVSATVVGDARVRGDVALPAFGVGGVLTVPAGHVLGPVDAAEVRREPVDPVIPCSCDAASQVDVSGLIARHVLDNDNAAIGLDATAMEDIEGERALELPCGRFHLTRITGTGRATITIRARTGLFIEDVVDLGEGLSVDVHAPGELDLFLGGAVAVAGPLTLGSTATPSRVRVYVAGSNVLALSAGSTLAGNLYAPRAALSLSGGAEVFGSVFVRQVEASGPLRLHYDADIRDAGAECTGD
>NZ_CP017169.1|WP_140854274.1|3484615_3485896_+|hypothetical-protein
MKREVKAGIAGLVFGSMLVGCGVAPEQGELGGVEDVTAGASASAETGLDAHRGSSTPVAVARYGHAVAYGDGKYFAVWADVRTGGIYGTRVKPDGTVLDPGGIRINFGEENGRRPAIAFNGTHFFVVWGTINGVDGVRVKPDGTLVGPMFRAVQSDEVFDPARVACSPKICLVTYTVAGDDSSTIYFTRVSKDGVILSTADRTLSASNTFADDASSTWNNSKKEFLAVWSVEQGDGPENADIYGNRVKEDGTILDGSGFPISAAEGAQTTPDVVWTGKSYQVVWSDDRNGNPDIYGARVSKTGTVKDPDGIPISTEVGAQTAPRIAHHNSKSLVVWDDTRYGPHSIWGARWGEDGDVWDGSGFPISSAGLAQQYLPDVAFGADKFFTIYAAQETYSPGDPHYIVGTRVTHQAQVNDVPAVPLTRRR
>NZ_CP017169.1|WP_140854276.1|3486221_3487529_+|hypothetical-protein
MFFKGRSHMNREVKAGIAGLLFGSMLAGCGVAPEQEWQGGVEDATAEAEALMSVETGPEEHRSRARPAALAKFGPAVAYGDGKYFTVWTDVRIGGIYGTRVKPDGTVLDKEGIRINIGDVEGFRPGIAFNGTHFFVVWESVDGIDAVRVKPDGTVVGPVFNVKQSGETVGPARVACSPKICLVTYTVSGDFSNIFFTRVTKDGVVLDTGDESLSASDTFANDASPTWNNKTKEFLVVWSDEHGEGPENADIYGNRVKEDGTILDGDGFPISQAEGAQTTPDVEWTHKNYQVVWTDDRNGNPDIFGARVSKTGMVKDPEGIPISTEEGAQAEPRLAHHNDKSLVVWDDTRDGPHRVWGARWGEDGDVRDPSGFPISTGDQPQEYLPDVAYGGGKFFVVYSGQETFEPLEPHFILGTRVTHQAEVKDVPALTLTRQR
>NZ_CP017169.1|WP_140854279.1|3488091_3489411_+|hypothetical-protein
MFLKGRLHMRREVKAGIAGLLFGSMLVGCGVAPEQEELGGVEDVTAESEAEAEAQMSAETGPEERRGYANPAPLARYWPAVAYGGGKFLAVWTDVRTGGIYGTRVKPNGTVLDKEDIRINIGDVEGFRPGIGFNGTHFFVVWESLNGVDAVRVKPDGTVVGPVFNVIQTGESVGPVRVACSPKICLVTYTISGDFSNIYFTRVTKEGVVLDTADQTLSASDTFANDASPTWNNKTKEFLVVWSDEHGEGPENADIYGNRVKEDGTILDGDGFPISQAEGAQTTPDVEWTHKNYQVVWTDERNGNPDIFGARVSKTGMVKDPEGIPISTAEGAQAEPRLAHHNDKSLVVWDDRRDGPHAVWGARWGENGDVWDPSGFPISTGDQPQEYLPDVAYGGGKFFVVYSGQETFEPLEPHFILGTRVTHQAEVKDVPALPLTRQR

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Crispr_ID: NZ_CP017169_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_9

5335408-5335550

Orphan

Consensus_repeat	Method
GGATGTGGAAGGAACGTTCCGTCCAG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP017169_9

>merge|NZ_CP017169|9|5335408-5335550|CRISPRCasFinder
GGACGCGGAAGAAACGCGCCCTCCGGGCAACTCCGCTGATTCCCCCCCCGGCGGCGTGGATGTGGAAGGAACGTTCCGTCCAGACCTTTCCGCAGAAACGGCCGCTGGAGCGAGGGCGGACGTGGAAGGAACGTTCCGTCCAG

>NZ_CP017169|9|8|5335408-5335550|CRISPRCasFinder
GGACGCGGAAGAAACGCGCCCTCCGG	GCAACTCCGCTGATTCCCCCCCCGGCGGCGT
GGATGTGGAAGGAACGTTCCGTCCAG	ACCTTTCCGCAGAAACGGCCGCTGGAGCGAGGGC
GGACGTGGAAGGAACGTTCCGTCCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140792627.1\|5324876_5325095_-\|DUF3185-family-protein	unknown	unknown	gnl\|CDD\|378652
NZ_CP017169.1\|WP_140800730.1\|5321808_5323008_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP017169.1\|WP_140792654.1\|5344259_5344796_-\|imidazoleglycerol-phosphate-dehydratase	unknown	unknown	gnl\|CDD\|153419
NZ_CP017169.1\|WP_140792645.1\|5338764_5340162_-\|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl\|CDD\|235798
NZ_CP017169.1\|WP_140855436.1\|5330363_5331596_+\|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl\|CDD\|238452
NZ_CP017169.1\|WP_140792635.1\|5331713_5332388_+\|GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|234745
NZ_CP017169.1\|WP_140855431.1\|5325147_5328681_-\|ribonuclease-R	unknown	unknown	gnl\|CDD\|273947
NZ_CP017169.1\|WP_140855433.1\|5328788_5330168_-\|protease-inhibitor-I42-family-protein	unknown	unknown	gnl\|CDD\|378179
NZ_CP017169.1\|WP_140792651.1\|5342722_5343502_-\|histidinol-phosphatase	unknown	unknown	gnl\|CDD\|273949
NZ_CP017169.1\|WP_140798741.1\|5333260_5334334_-\|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl\|CDD\|319743
NZ_CP017169.1\|WP_140792656.1\|5344792_5345509_-\|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase	unknown	unknown	gnl\|CDD\|240083
NZ_CP017169.1\|WP_140792649.1\|5341397_5341847_-\|DofB-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140792623.1\|5323155_5323941_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017169.1\|WP_140855440.1\|5340179_5341379_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140855429.1\|5324116_5324860_+\|DUF2807-domain-containing-protein	unknown	unknown	gnl\|CDD\|371327
NZ_CP017169.1\|WP_140792637.1\|5332437_5333271_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293801
NZ_CP017169.1\|WP_140792653.1\|5343498_5344260_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	unknown	unknown	gnl\|CDD\|234996
NZ_CP017169.1\|WP_140792650.1\|5342114_5342723_-\|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE	unknown	unknown	gnl\|CDD\|235067
NZ_CP017169.1\|WP_140798744.1\|5336258_5337515_-\|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl\|CDD\|237001
NZ_CP017169.1\|WP_090490647.1\|5337575_5338505_-\|lipoyl-synthase	unknown	unknown	gnl\|CDD\|235493

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140792627.1\|5324876_5325095_-\|DUF3185-family-protein	gnl\|CDD\|378652	pfam11381, DUF3185, Protein of unknown function (DUF3185). Some members in this bacterial family of proteins are annotated as membrane proteins however this cannot be confirmed. Currently no function is known.	3.25368e-14
NZ_CP017169.1\|WP_140800730.1\|5321808_5323008_+\|metallophosphoesterase	gnl\|CDD\|277331	cd07385, MPP_YkuE_C, Bacillus subtilis YkuE and related proteins, C-terminal metallophosphatase domain. YkuE is an uncharacterized Bacillus subtilis protein with a C-terminal metallophosphatase domain and an N-terminal twin-arginine (RR) motif. An RR-signal peptide derived from the Bacillus subtilis YkuE protein can direct Tat-dependent secretion of agarase in Streptomyces lividans. This is an indication that YkuE is transported by the Bacillus subtilis Tat (Twin-arginine translocation) pathway machinery. YkuE belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	5.05438e-77
NZ_CP017169.1\|WP_140792654.1\|5344259_5344796_-\|imidazoleglycerol-phosphate-dehydratase	gnl\|CDD\|153419	cd07914, IGPD, Imidazoleglycerol-phosphate dehydratase. Imidazoleglycerol-phosphate dehydratase (IGPD; EC 4.2.1.19) catalyzes the dehydration of imidazole glycerol phosphate to imidazole acetol phosphate, the sixth step of histidine biosynthesis in plants and microorganisms where the histidine is synthesized de novo. There is an internal repeat in the protein domain that is related by pseudo-dyad symmetry, perhaps as a result of an ancient gene duplication. The apo-form of IGPD exists as a catalytically inactive trimer which, in the presence of specific divalent metal cations such as manganese (Mn2+), cobalt (Co2+), cadmium (Cd2+), nickel (Ni2+), iron (Fe2+) and zinc (Zn2+), assembles to form a biologically active high molecular weight metalloenzyme; a 24-mer with 4-3-2 symmetry. Each 24-mer has 24 active sites, and contains around 1.5 metal ions per monomer, each monomer contributing residues to three separate active sites. IGPD enzymes are monofunctional in fungi, plants, archaea and some eubacteria while they are encoded as bifunctional enzymes in other eubacteria, such that the enzyme is fused to histidinol-phosphate phosphatase, the penultimate enzyme of the histidine biosynthesis pathway. The histidine biosynthesis pathway is a potential target for development of herbicides, and IGPD is a target for the triazole phosphonate herbicides.	1.08426e-63
NZ_CP017169.1\|WP_140792645.1\|5338764_5340162_-\|dihydrolipoyl-dehydrogenase	gnl\|CDD\|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP017169.1\|WP_140855436.1\|5330363_5331596_+\|molybdopterin-molybdotransferase-MoeA	gnl\|CDD\|238452	cd00887, MoeA, MoeA family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF), an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MoeA, together with MoaB, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes.	1.01321e-161
NZ_CP017169.1\|WP_140792635.1\|5331713_5332388_+\|GTP-cyclohydrolase-II	gnl\|CDD\|234745	PRK00393, ribA, GTP cyclohydrolase II RibA.	4.10325e-106
NZ_CP017169.1\|WP_140855431.1\|5325147_5328681_-\|ribonuclease-R	gnl\|CDD\|273947	TIGR02063, Ribonuclease_R, ribonuclease R. This family consists of an exoribonuclease, ribonuclease R, also called VacB. It is one of the eight exoribonucleases reported in E. coli and is broadly distributed throughout the bacteria. In E. coli, double mutants of this protein and polynucleotide phosphorylase are not viable. Scoring between trusted and noise cutoffs to the model are shorter, divergent forms from the Chlamydiae, and divergent forms from the Campylobacterales (including Helicobacter pylori) and Leptospira interrogans. [Transcription, Degradation of RNA].	0
NZ_CP017169.1\|WP_140855433.1\|5328788_5330168_-\|protease-inhibitor-I42-family-protein	gnl\|CDD\|378179	pfam09394, Inhibitor_I42, Chagasin family peptidase inhibitor I42. Chagasin is a cysteine peptidase inhibitor which forms a beta barrel structure.	1.50571e-12
NZ_CP017169.1\|WP_140792651.1\|5342722_5343502_-\|histidinol-phosphatase	gnl\|CDD\|273949	TIGR02067, his_9_HisN, histidinol-phosphatase, inositol monophosphatase family. This subfamily belongs to the inositol monophosphatase family (pfam00459). The members of this family consist of no more than one per species and are found only in species in which histidine is synthesized de novo but no histidinol phosphatase can be found in either of the two described families (TIGR01261, TIGR01856). In at least one species, the member of this family is found near known histidine biosynthesis genes. The role as histidinol-phosphatase wsa first proven in Corynebacterium glutamicum. [Amino acid biosynthesis, Histidine family].	1.38736e-100
NZ_CP017169.1\|WP_140798741.1\|5333260_5334334_-\|lipoyl(octanoyl)-transferase-LipB	gnl\|CDD\|319743	cd16444, LipB, lipoyl/octanoyl transferase. Lipoate-protein ligase B is a octanoyl-[acyl carrier protein]-protein acyltransferase the catalyzes the first step of lipoic acid synthesis. It transfers endogenous octanoic acid attached via a thioester bond to acyl carrier protein (ACP) onto lipoyl domains, which is later converted by lipoate synthase LipA into lipoylated derivatives.	1.32797e-97
NZ_CP017169.1\|WP_140792656.1\|5344792_5345509_-\|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase	gnl\|CDD\|240083	cd04732, HisA, HisA. Phosphoribosylformimino-5-aminoimidazole carboxamide ribonucleotide (ProFAR) isomerase catalyzes the fourth step in histidine biosynthesis, an isomerisation of the aminoaldose moiety of ProFAR to the aminoketose of PRFAR (N-(5'-phospho-D-1'-ribulosylformimino)-5-amino-1-(5''-phospho-ribosyl)-4-imidazolecarboxamide). In bacteria and archaea, ProFAR isomerase is encoded by the HisA gene.	1.2552e-84
NZ_CP017169.1\|WP_140792623.1\|5323155_5323941_+\|hypothetical-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	6.95113e-07
NZ_CP017169.1\|WP_140855429.1\|5324116_5324860_+\|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).	3.25006e-32
NZ_CP017169.1\|WP_140792637.1\|5332437_5333271_+\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293801	cd07715, TaR3-like_MBL-fold, MBL-fold metallo-hydrolase domain of Myxococcus xanthus TaR3 and related proteins; MBL-fold metallo-hydrolase domain. Myxococcus xanthus Tar3 may function as an ammonium regulator/effector protein involved in biosynthesis of the antibiotic TA. Some are members of this subgroup are annotated as ribonucleases. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions.	1.05364e-115
NZ_CP017169.1\|WP_140792653.1\|5343498_5344260_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	gnl\|CDD\|234996	PRK02083, PRK02083, imidazole glycerol phosphate synthase subunit HisF; Provisional.	1.28791e-155
NZ_CP017169.1\|WP_140792650.1\|5342114_5342723_-\|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE	gnl\|CDD\|235067	PRK02759, PRK02759, bifunctional phosphoribosyl-AMP cyclohydrolase/phosphoribosyl-ATP diphosphatase HisIE.	8.31558e-87
NZ_CP017169.1\|WP_140798744.1\|5336258_5337515_-\|2-oxo-acid-dehydrogenase-subunit-E2	gnl\|CDD\|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	9.70905e-174
NZ_CP017169.1\|WP_090490647.1\|5337575_5338505_-\|lipoyl-synthase	gnl\|CDD\|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	7.07392e-176

>NZ_CP017169.1|WP_140798741.1|5333260_5334334_-|lipoyl(octanoyl)-transferase-LipB
MNTITVYRLGRVEYEDGLALMHLFSESRRQGLSGDVLLLLEHPPILTLGRAAKRENIVASDAQLAKEGAEVFETNRGGDVTYHGPGQLVGYPIFLLPEDRRDVRRYVRDVERSVMQVLAQWGITAGPIPKWPGVWIGAEGAPDARKIAAIGVHLSRWLTTHGFALNVNTNLDHFQLIVPCGIREAGVTSMQRELGRALPMAEVEEAIAISFCTVFDSERVDAPPPMRTVSIAVVKGRGPEARVLLVRRRPERGGFWQVLTGRLEAGESPAEAAARELEEETGLRVPLVDLDYRHAFALGEALPPQLVEENGFAVHVPPDADVRLGAEHDAFEWVDVPTALERLPFRGLRETVKRATA
>NZ_CP017169.1|WP_140792637.1|5332437_5333271_+|MBL-fold-metallo-hydrolase
MPFEVRFWGVRGSIPSPGAHTKRYGGNTPCVEVRCGDELLIFDLGTGARALGHALVAKKKPVKGSIFISHYHYDHLQGLPFFGPMFLPSSDLTVYGPARHGQSVKQLLSGQMVPPYFPVTADGVFRAQLTYTDLAATQTLQLGPATVRTIELNHPGGNMGYRVECQGRSVVYATDLEHGSDMDAAFYAFAQDADVLIYDAMYTEDEYHGRTGPARTGWGHSTWQAAVHAADEAGVKKLVLFHHDPSRDDAGMDRLLRQVRKHRPDAIAARESLVIKL
>NZ_CP017169.1|WP_140792635.1|5331713_5332388_+|GTP-cyclohydrolase-II
MSDTRSPQVLPTRKPTQHLERFSEADIPTERGSLRTIVFRDKRNGREHVALVVGEVSGHEGVPVRIHSECLTSEVFGSLKCDCREQLDRSLDFITQSGQGVVLYLRQEGRGIGLGNKIKAYALQSKGLDTYEANRQLGFADDLRTYDIAAEMLRSLDVRSVDLMTNNPLKIAGIVEEGIPVRRRIPSRTEHNPHNVDYLRTKRERTGHLIELFAEDDDTEAQAG
>NZ_CP017169.1|WP_140855436.1|5330363_5331596_+|molybdopterin-molybdotransferase-MoeA
MNDSATLLPEEDARSQILALCAPLPTEWLLLDDALGRVLAEDVMAQRTLPPWDNSAMDGYAVRSADLAGPLPVRLNVGETIYAGAVGHQALVPGVCARIMTGAPLPAGADAVVMRERTRPVVQSGADQVDVLEAVAPGQFVRPRGEDAREGQLLLARCTPLGIPELGLLWAQGRQAVPVSRAPRVAILSTGDELCHADEPPNGRIVDTNAPSLALAVRRAGGIPTRLGIARDTRDAVLAALSRLDGFDVVLTSAGVSVGERDCVKEVLAELGVEQHFWRVAIKPGKPLVVGRRGATLFFGLPGNPTSSLVTFELFVRPALRKLLGHAQVGPGRVAGRLEGKLSKPSGLAHFVRVTAAWREGSLWARPLATQTSGALRSAAAATHLLHFPREASSLTAGDAVELLPLSWVA
>NZ_CP017169.1|WP_140855433.1|5328788_5330168_-|protease-inhibitor-I42-family-protein
MAKPKSGAKKTTPAGKAGAKPAAKKDSAARLDLIKNASKRVAKAATKLAKAASDVTKGAKSAVKKAVQEKATAKKAAPAGKTASAAKAASPAAKTPKASPAKAPPAAKSAAGAKAGKASAVPAAPPVERPRPRATKLPPPGEPLTKREMEQLLTAGEGRGVTGEGSLKGRLVVTNDMPHLVVVGRDKRELTFLLQGPDQEVLPAYVDHKVSVSGLIRKTTNHAGVVDVRKYSAKKPDSEVVEAAPVETEARLRYLSPGEVSMVTAAGMGAGIKGFAGVRGNLEMTGEEFVLVVSNGGTRQQVSFIIEGKAAGKALRKHVGYTLQVQGVVDKTSGWGGRILAENVELRPSEARAVSRDEMELVHIEGEVPTSVDVRLNHGLAVRLPEHPGFTWAIEPTVAKRVGLREANFEPAPEDGPGTREFFFTPRNPGTFEVEFFLAKALSPGLVDRSFKINVTVKP
>NZ_CP017169.1|WP_140855431.1|5325147_5328681_-|ribonuclease-R
MSLSQDLLKQILAEADHPLGIKELLRLAGLHPGQQTELKRALRELVRQGDILKDGKRFVPRQPSRREADVRAREQGAPMAWRQRDAEGPRESGPGRGPRQAGQRAAGPGGFAARRHEPGARGKRAGWQEQGPGRERKGASKHGGGFRQERGEWPGRRGRFSEVEEDGLLEGILHVHRDGFGFVHPLSGEGDNVFLPPHEAQRALDNDRVVVAVSGRPPRLEGRIVRVVQRRRELAVGTYVVKGRYAVVYPTDSSLPGPIRVPLTQMAREGDLVKVQLGIGAQMLDPDRGLHGEVAGSLGKPGTPSAEVLGVAYSQGFSDEFPPEVMGEADRYAVTVSEEEARGEHRRDLRALPLITIDGEDARDFDDAVYVEDQADGWRLVVAIADVTHYVWEGSALNAEALRRATSVYLPDRVLPMLPERLSNGICSLRPDEDRLCMVADMTFDRRGHRRSYDLYPAVMRSVARCTYNEVQDVLDGKDVPHRNAHKPHFERLMSLARALMKMRKERGAIDFDLPEHKVVLDEEGLPARMDKRERKDSHRLIEECMLAANEAVATFFQDEGLPTVYRFHGEPDPEKLATFAALAEAYGFKMRVEDGVSSKELDAFVSQLQGHPEQRALNQLLLRSMMQAVYTSSRVGHYGLAAEHYLHFTSPIRRYPDLLVHRLLKAHWARKGRKPSQSMLEREEDQLEDMSAQCSERERAAMQVEREVVSFYACLLMKDRVGEEFAATVAAITDFGFFVELDEVHVEGLVKAETLGPGAKLDKLTHSLVYANGRRVRVGQKLRVRLTSVNVTAKKIDFEALQFEGEALLSRVATRGDQPHRRQAWTAEAPSHRERDGRRERAGRPGRREREAAATSQGAPSGHHEETGTGRPRGRFSREGRREEAAPHRKEPRFPPRAPEGQEPPRAESPAWPKRRTFIRPEPQAPAPVSAETAEPLPSEAPSAPASWELPAGDDAARSPHPGFDRIRALASQRQRGPEPRGASHGRSFQKQKPQGGPGPRFPAPKPGRESEDDRAFSIEPPRPPPEAPIEAPPPVPSRAVTETPTPVAPEPVRAAPASVETPVTPAPAPETAAPKRKATRKKAVAKATRTPARKKTTAAGSAKKAAATKAKKPTAKAKKAAPARAAAKATKVAASKSKAKAPSKKAAKPTVARAAKPAKASGAAKKKAPTGRKKR
>NZ_CP017169.1|WP_140792627.1|5324876_5325095_-|DUF3185-family-protein
MSFVRLLGVMLAIAGAVLLWSGLKARDSLAERATELFTGRNTDRTTLYLAGGGAALVGGILMVLAGGGRRRR
>NZ_CP017169.1|WP_140855429.1|5324116_5324860_+|DUF2807-domain-containing-protein
MRIAKSGAWVGTALLAVALTACSSGPFVEGNGRVVESEREIPSFDEVVVNDGISATVVVDPVQPASVIVEGDSNLVSLMRTEVLSGAMLRVHFLADDVGHWESANPLRVRITVPTLTSFQRSGGGTADLSGSIDVPSFLLTASGGGTIRARGFVTERLTLETSGGAETTLEGQATLLDSEMSGGGRLFATGLQTRDARLESSGGGTTEVRVSGSLRVEASGGADIRITGGPTVVEKDLSGGSALRFE
>NZ_CP017169.1|WP_140792623.1|5323155_5323941_+|hypothetical-protein
MKRLGKVGLLVGALTLGGAVVGCKAEDDTAKKHRIVGSDHLSKKEFKEAAAAYALSLQADPKQEKVWEKKAFAHMQLGQMNEAAEAVLKMGEFKTTPTEKAEIYRTLASMYMTGGTTEEAEKYFNEALKLEPKDEASLGWIAEIYAQRGGARSMGAPIIKESLEKSLSYYDQVIAINPNSANTYLNKRVVMGRLMEFERQQKEMALSEATENAKNKEVVAEATARADEHQKRMDEYQVQFAEMTKKFSEAQKAAKAAAPAQ
>NZ_CP017169.1|WP_140800730.1|5321808_5323008_+|metallophosphoesterase
MPVRLFSFSMLIGLGAVLGHLYLYRRLVRPLLPGRLPRLLALAVLVAMTGVLGFRRTVLDLLPESAEGLLTMAVYAWMGVALCLVIALLLTDVGRGLAALARRVRPHASPAPPSPAPSTTVDEDRRRFLGQAVAGSAFVAGGGLATYGSWRAFSPPLVTELAVKIPKLPKALDGLSIVQLTDIHVGHFIQRRYMDALVQQANSLRPDLFAITGDLVDGDVASLGGHVAALAALKSRYGSYFVTGNHDYYSGDEEWSAFLESLGIEVLRNRHVRIGDAGASFDLVGVDDWSGGRRRNKKGYDLDQALAGRAPDRAAVLLAHQPANFKVAAERGVDLQISGHTHGGQLVPMTLLIGLAWEHSAGLYAHGDSNIYVSRGCGFWGPPMRVGSPPELVKLVLTA
>NZ_CP017169.1|WP_140798744.1|5336258_5337515_-|2-oxo-acid-dehydrogenase-subunit-E2
MAIFEFKLPDLGEGVMEGELVKWHVKAGDSVKEDQVLAEVMTDKATVTVPAPKAGRVVKTHGNEGDMAKVHQLLVTLEVEGDAPAQAGGHGEASAPAAAPVAAAGGHGGGAPASASKVLATPVTRRMAREHGLDLAAIAGTGPQGRVTKADVVAALEGGEKNVVAAPAEQKARPAAPAVSSGAADERVPLRGLRKKIAEKMVRSKFTAPHFAFVEEVDATELVALRARLNAQLAAAGENTKLNYLPFIIKATVAALKKFPHLNANFDEASQELVVRGEYNIGMAAATPDGLTVAVVKNADRLTLAELARETARLGAAARDRKLKMEELTGGTFTISSLGQSGGLFATPIINHPEVGILGVHRLKKRPAVVGDQVVVRDMMNLSLSCDHRVIDGSVAADFTYEIIKYLEKPDLLFLAMA
>NZ_CP017169.1|WP_090490647.1|5337575_5338505_-|lipoyl-synthase
MATPDRFPLPQVTETTRKPEWLKVRLPHGEGYERVKAIVKRTKLATVCEEARCPNIAECWGGGTATVMLMGEVCTRACRFCHVKVGAPPPLDPMEPIHLAQAVKEMDLEYIVVTSVNRDDRPDGGASHFASAIRELRRESPRTIVEVLIPDFKGVEKDLTTVAEAKPHVVAHNVETVERLTPTVRDRRAKYHQSLRVLEYLKNRPEGLYTKTSVMVGLGETDAELEQTFKDLRDVGVDVLTLGQYLQPSQYHLRVERFVSPAQFEAYKTLAESYGFLYVASGPLVRSSYRAAEFFMKGLMERERLERLG
>NZ_CP017169.1|WP_140792645.1|5338764_5340162_-|dihydrolipoyl-dehydrogenase
MAETFDVVIIGSGPGGYVGAIRAGQLGLKTAIIEKDKRLGGTCLHRGCIPTKSLLWTAELFHHVREAADFGVDVSSPAINWPNAMKHKDKIVTKGANGIDFLMKKNKVTVVKGHGRIAGKGKVEVTAADGSKQVLEAKNIIIATGSVPKSLPNVPVDHKRVLNSDSILQIDRVPKSIIVLGAGAVGCEFASVFNHVGSKTSIVEYLPALLPIEDADISKELEKIFKRRGIDVHTGSAVEKVEHTADGVRVTMKVGNETKTLEAEILLSAVGRSPVTEDVGLDKTNIQAERGYIKVDSMLRTSEPNVYAVGDIIPTPMLAHMASAECVVAVEHIAGKNPQPINYDLTPSATYCYPEVASVGLTEKKAKERGYDVKVGIAPMGAVTKAAISNEATGMIKIVSDRKYDEVLGVHLIGPHATELLAEACVALKLEITTEELANTIHAHPTLSEIVHEGAEATLGHPRHF
>NZ_CP017169.1|WP_140855440.1|5340179_5341379_+|hypothetical-protein
MRMEPGGADNPRSRLESRSLLVRRFPLRTLLLMLAALIAFGRLWCVTHQEEAPGPRPERMAQAGDAPAGAPVPSSAPECLTLERALESALRTPQDTRVLDEARQQLDACRQPPVRACALGVALDARSPLSEGEATPLRGLLTSLCERCPPAANSCARAVGQALLSAAVGSNADIASAKWNLEHAGPGLGGACASLVQLGLAPAAQSDLTVRPPVLALTGELAPRCSQAGFLDDALLRAAAVNLVAPTPALVALAAVPIPPETSAMKPDRIEGTEPGFQAFDRDENTGVPVGKALKSERWAADGALRASYAPTLKQLVSMRIRATGPGTVRAIVRTPEGVGLKDPEKDFAFVNPTVCRFTGTGQWEQCPLQVPLRDVDAVSVFPERADTELKELEVRGAR
>NZ_CP017169.1|WP_140792649.1|5341397_5341847_-|DofB-protein
MNGPTYKAEIIDRVIFSRWENPPTKEDVTLVLAQMQEAATRLNTNLIYVGSVSSKSKVPDANERTVLNQFLMDARRTCVEQAWLIYEGTDLQHNLQRVIISGVLILTRTFDNFLSVAKSGDSIVKDVSAVLKKDAAPLFTMAKERGLVA
>NZ_CP017169.1|WP_140792650.1|5342114_5342723_-|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE
MFDLDALDFAKGNGLVTVVTQDASTGDVLMVAHADREALERTLATGELHYRSRTRGLWHKGATSGNVQRVVALRADCDGDAVLARVEKAGPACHTGTETCFGPGRWDALSALDDTLARRAAPVERPDDAPPSYTRRLLEDRNLRLKKLGEEAAELVTACADADPSRAAEEAADVLYHVLVAVRPLGLSLDDVKAVLARRAPR
>NZ_CP017169.1|WP_140792651.1|5342722_5343502_-|histidinol-phosphatase
MTDSGNLMQAAAEVARMAGDAALGFFRGGIAVDTKSDGSPVTVADRTAESRAREWLEARFPQDGILGEEFGETRPGAKRRWILDPIDGTKTFIRGVPLWGTLVALAEGERILVGAAYFPAVSELLVAAPGQGCFWNDQRAAVSTQAELSQAVVLSTDERFPVYPERGAAWRALARDAAVDRTWGDCYGYLLVATGRAEVMVDELLSPWDGAALQPIIEEAGGVFTDWTGRRTAFGGNGIATNAAMARVVRERLGAVETR
>NZ_CP017169.1|WP_140792653.1|5343498_5344260_-|imidazole-glycerol-phosphate-synthase-subunit-HisF
MLTRRLVVCLDVKGGRVVKGVQFEGLRDVGDPVELARRYEAEGADELTFLDISASAEERDTLWELVRRTAEQLFIPLAVGGGVRTVDDVGRALRAGADKVSINSAAVANPALLTACAERFGAQCVVASIDAKRDGDRWRVYTHGGRKPTDLDAVAWARECVARGAGEVLLTSIDRDGARTGYDLALTRAVSEAVDVPVIASGGAGSAAHVRDAFQEGGADAALVAGILHDGLTTVGAIKALLREGGLHIRSVA
>NZ_CP017169.1|WP_140792654.1|5344259_5344796_-|imidazoleglycerol-phosphate-dehydratase
MTTVIRETKETQVRVELSPGKGVTNVDTGLKFFDHMLATFARYAGLDLSLHARGDLTHHVMEDVAITLGTAVQQVIPATAARFAERTIPMDDALVQACLDAGGRFYYQGPLKNRLYEHWMRSFSEHARVTLHLRVLRGKDSHHATEASFKALGLALRDAMVDSGSVFSMKGAVSLEVK
>NZ_CP017169.1|WP_140792656.1|5344792_5345509_-|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase
MIAIPAIDLREGACVQLVGGSFAAEKVRVEDPLEALKQWRRHGFRAFHVVDLDAALGKGSNSDAIFQLTAYERGLTFSVGGGVRDSDRVEAILSGGAEFVVVGTRAIEDAGWLADIANRFPGRVVVAADVKGREVVTRGWTEGSHRDIREVLAAFKPLPLAGLLVTAVHKEGQLSGVDLPLMREVASTSRHRLYASGGVTTLEDLRALAAAGAYGAVIGMALYTGRLDASAVAREFAG

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Crispr_ID: NZ_CP017169_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_10

6429720-6429823

Orphan

Consensus_repeat	Method
GCTTCCGCGAGCTGCGCTTCGAGTTCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_10

>merge|NZ_CP017169|10|6429720-6429823|CRISPRCasFinder
GCATCGGCGAGCCGCGATTCCAGCTCCGCTTGCTGTGCTTCGAGTCGAGCGTTGAGGTCCGCCAGCCGGGTCTCCGATTCAGCGCGCTGTGCCTCGGCGTGGGC

>NZ_CP017169|10|9|6429720-6429823|CRISPRCasFinder
GCATCGGCGAGCCGCGATTCCAGCTCCG	CTTGCTGTGCTTCGAGTCGAGCGTTGAGGTCCGCCAGCCGGGTCTCC
GATTCAGCGCGCTGTGCCTCGGCGTGGGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140856115.1\|6438931_6439942_+\|ribonucleotide-diphosphate-reductase-subunit-beta	unknown	unknown	gnl\|CDD\|153108
NZ_CP017169.1\|WP_140794192.1\|6426086_6427937_-\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017169.1\|WP_140856110.1\|6434946_6435900_+\|IF-2-protein	unknown	unknown	gnl\|CDD\|237057
NZ_CP017169.1\|WP_161606787.1\|6442217_6443099_+\|AHH-domain-containing-protein	unknown	unknown	gnl\|CDD\|379603
NZ_CP017169.1\|WP_140794193.1\|6427975_6428827_-\|diaminopimelate-epimerase	unknown	unknown	gnl\|CDD\|234768
NZ_CP017169.1\|WP_140856120.1\|6441172_6441637_+\|DUF4150-domain-containing-protein	unknown	unknown	gnl\|CDD\|372665
NZ_CP017169.1\|WP_140794187.1\|6422648_6423422_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225375
NZ_CP017169.1\|WP_140858472.1\|6441754_6442189_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140856101.1\|6420866_6422480_-\|sigma-54-interacting-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017169.1\|WP_140794181.1\|6419799_6420219_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_161606789.1\|6443739_6445098_+\|TIGR02270-family-protein	unknown	unknown	gnl\|CDD\|131323
NZ_CP017169.1\|WP_140856099.1\|6420334_6420682_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_161606790.1\|6446221_6446983_+\|immunity-49-family-protein	unknown	unknown	gnl\|CDD\|373949
NZ_CP017169.1\|WP_140856113.1\|6436338_6438855_+\|ribonucleoside-diphosphate-reductase-subunit-alpha	unknown	unknown	gnl\|CDD\|178056
NZ_CP017169.1\|WP_140856118.1\|6440080_6441127_+\|DUF2169-domain-containing-protein	unknown	unknown	gnl\|CDD\|370755
NZ_CP017169.1\|WP_140799406.1\|6424567_6426067_-\|DUF4388-domain-containing-protein	unknown	unknown	gnl\|CDD\|373017
NZ_CP017169.1\|WP_161606788.1\|6443126_6443726_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140856104.1\|6423472_6424000_+\|SHOCT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378276
NZ_CP017169.1\|WP_140856106.1\|6424021_6424555_+\|SHOCT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378822
NZ_CP017169.1\|WP_140856097.1\|6416122_6419794_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140856115.1\|6438931_6439942_+\|ribonucleotide-diphosphate-reductase-subunit-beta	gnl\|CDD\|153108	cd01049, RNRR2, Ribonucleotide Reductase, R2/beta subunit, ferritin-like diiron-binding domain. Ribonucleotide Reductase, R2/beta subunit (RNRR2) is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. The RNR protein catalyzes the conversion of ribonucleotides to deoxyribonucleotides and is found in all eukaryotes, many prokaryotes, several viruses, and few archaea. The catalytically active form of RNR is a proposed alpha2-beta2 tetramer. The homodimeric alpha subunit (R1) contains the active site and redox active cysteines as well as the allosteric binding sites. The beta subunit (R2) contains a diiron cluster that, in its reduced state, reacts with dioxygen to form a stable tyrosyl radical and a diiron(III) cluster. This essential tyrosyl radical is proposed to generate a thiyl radical, located on a cysteine residue in the R1 active site that initiates ribonucleotide reduction. The beta subunit is composed of 10-13 helices, the 8 longest helices form an alpha-helical bundle; some have 2 addition beta strands. Yeast is unique in that it assembles both homodimers and heterodimers of RNRR2. The yeast heterodimer, Y2Y4, contains R2 (Y2) and a R2 homolog (Y4) that lacks the diiron center and is proposed to only assist in cofactor assembly, and perhaps stabilize R1 (Y1) in its active conformation.	2.13152e-103
NZ_CP017169.1\|WP_140794192.1\|6426086_6427937_-\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	2.45621e-27
NZ_CP017169.1\|WP_140856110.1\|6434946_6435900_+\|IF-2-protein	gnl\|CDD\|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	0.000317524
NZ_CP017169.1\|WP_161606787.1\|6442217_6443099_+\|AHH-domain-containing-protein	gnl\|CDD\|379603	pfam14412, AHH, A nuclease family of the HNH/ENDO VII superfamily with conserved AHH. AHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif, AHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. Like WHH and LHH, the AHH nuclease contains 4 conserved histidines of which, the first one is predicted to bind a metal-ion and the other three ones are involved in activation of a water molecule for hydrolysis.	0.00603012
NZ_CP017169.1\|WP_140794193.1\|6427975_6428827_-\|diaminopimelate-epimerase	gnl\|CDD\|234768	PRK00450, dapF, diaminopimelate epimerase; Provisional.	1.52191e-97
NZ_CP017169.1\|WP_140856120.1\|6441172_6441637_+\|DUF4150-domain-containing-protein	gnl\|CDD\|372665	pfam13665, DUF4150, Domain of unknown function (DUF4150).	1.70847e-47
NZ_CP017169.1\|WP_140856101.1\|6420866_6422480_-\|sigma-54-interacting-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	7.34556e-92
NZ_CP017169.1\|WP_161606789.1\|6443739_6445098_+\|TIGR02270-family-protein	gnl\|CDD\|131323	TIGR02270, hypothetical_protein_GSU3180, conserved hypothetical protein. Members are found in Myxococcus xanthus (six members), Geobacter sulfurreducens, and Pseudomonas aeruginosa; a short protein homologous to the N-terminal region is found in Mesorhizobium loti. All sequence are from Proteobacteria. The function is unknown. [Hypothetical proteins, Conserved].	2.37233e-53
NZ_CP017169.1\|WP_140794187.1\|6422648_6423422_+\|alpha/beta-hydrolase	gnl\|CDD\|225375	COG2819, COG2819, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	1.13889e-34
NZ_CP017169.1\|WP_161606790.1\|6446221_6446983_+\|immunity-49-family-protein	gnl\|CDD\|373949	pfam15575, Imm49, Immunity protein 49. A predicted immunity protein with an all alpha-helical fold and a conserved proline residue. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REAse-1 or Tox-REase-6 families.	1.3404e-08
NZ_CP017169.1\|WP_140856113.1\|6436338_6438855_+\|ribonucleoside-diphosphate-reductase-subunit-alpha	gnl\|CDD\|178056	PLN02437, PLN02437, ribonucleoside--diphosphate reductase large subunit.	0
NZ_CP017169.1\|WP_140856118.1\|6440080_6441127_+\|DUF2169-domain-containing-protein	gnl\|CDD\|370755	pfam09937, DUF2169, Uncharacterized protein conserved in bacteria (DUF2169). This domain, found in various hypothetical prokaryotic proteins, has no known function.	5.50692e-109
NZ_CP017169.1\|WP_140799406.1\|6424567_6426067_-\|DUF4388-domain-containing-protein	gnl\|CDD\|373017	pfam14332, DUF4388, Domain of unknown function (DUF4388). This domain family is found in bacteria, and is typically between 102 and 135 amino acids in length.	8.86263e-29
NZ_CP017169.1\|WP_140856104.1\|6423472_6424000_+\|SHOCT-domain-containing-protein	gnl\|CDD\|378276	pfam09851, SHOCT, Short C-terminal domain.	2.23681e-06
NZ_CP017169.1\|WP_140856106.1\|6424021_6424555_+\|SHOCT-domain-containing-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.	1.34026e-05
NZ_CP017169.1\|WP_140856097.1\|6416122_6419794_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	9.38282e-89

>NZ_CP017169.1|WP_140794193.1|6427975_6428827_-|diaminopimelate-epimerase
MEARERIFKYQGLGNDFVVLDRRGSGEDIDAATSRWMCDRRLGIGGDGVLALLPSERGVARMVVHNADGSIAEMCGNGLRCAVKFLVDDSGQTPGHLDVETGAGVLTCYPSYGEGGVVAVDISMGPARLVAPNLPSGVTGQPFLDAFVPGHPHLRAYAVSMGNPHMVLLDQPLEDASRLGPLLERHPSFPDRTNVEFVRVDSDGLTVVVWERGCGLTQACGTGACASAVAAVLAKRLPADAWLRVTLPGGDLRIRVPADLSDIRLRGPVAFVFEGVVAVPSGR
>NZ_CP017169.1|WP_140794192.1|6426086_6427937_-|response-regulator
MAGPILVVDDDLFFRQLASDLLTHNGHRVVAVENATLALEEAARTPFDLVITDVVMPGVDGFALTARLRERDPDQEVILVSHRTDIRNSEVALRSGAADCLTKPVDANDMLLAVDRALERASLRRERTQLRDENLEFARFHNLHQRCLELLSHPDLEWLQERLTSELAAICDAQSAALWVVDDRGDLVLRAYRGLLDRQFLAEKMSPEGPLSGRLREAQPWLARDERSSVMYVPLVASGEVVGLAQLSDPLSGDFRPEHSRDARVLGDFAAVGLKNGRKMLALQRLGLRDRETAAYNLSYFTDYASKEIYKARRYGRTFSLLTFSIDNLPLVRVRQGAADAKKAVRGIIKALSKIIRDSDVIAKASDQEFYLLLPETDFFGALMFVRRAVAAVREEPEAMEVDQRLPLAMVGGASTFPKDGEDFDELVHRCRRRMDERRASLQRRLMLDGLPFWDEVDLLLGTPNSPRLPVDERSEPSRRGKVSDVLFDELQAEIAREMMRDPGSRGLLYVGGPEIRTDLNIAAGLESAPPDLASRIYLLGRRVDLESHPALTPVFLEGDDRIARHEFILWLSENAAYALIQRRGHGATWGFHTSDTAVVDGLISKLQAEYDLQPY
>NZ_CP017169.1|WP_140799406.1|6424567_6426067_-|DUF4388-domain-containing-protein
MAPVRKILIADPDLESVRSLSRALRTKGYQVHYAPDGSRALEVAVLRHPDLTLFDEGCRLLDARTFIQILRTNPRTEDIPVVLTTASFESDRLRGLRDGYLRKPFNLDEVLSRIEHIFRRSEAAKDLKSEQQEIEGSLSQLSIPDLMQLLGMNRRSGRLTLERGNDRGEISVVEGRPVNAKLGRVEGEKALFRLLAWVDGTFTFSPGGNTARPRINRGMDDALLEGMRQSDEVNRLMPGLPPRHTRLMLAPDADLQGDQHPVTQQVVDLLRHPRALGEVLDLAPATDLEVLNVLTTLMQRGVAKAADGDGVEAASGELLGAAEVHALRGRILRTRAPAKVATAKIFVCGSGASAARRVLSRMPGMEALSADPTAVKSGFGTLGRLVLSEVLRLDFCVLPPAEAARPLWRPFTAGAMGALLMDVAEPSVRLARYLAWEVRMPVVVVGAEVPAALQGAPAGALGAADDLADALRSLLVQALNPAPTLPGVPQVQRAAASIV
>NZ_CP017169.1|WP_140856106.1|6424021_6424555_+|SHOCT-domain-containing-protein
MLTAVLAMLPFLLFSLVGFGVAGYFFYAHAQTQRLREHGTAGEATILRMERTSMRINKSYVYDFLLEFKVPGLPTYRRQHRSRAHDWKAFILEPGVRLKVKIDPNDPQRFVVLGPVDEQRPQIIQALIAGAAGFSESRTVAPSDPVKALKDLQSMLDNELITQDEYARKKAEILSRL
>NZ_CP017169.1|WP_140856104.1|6423472_6424000_+|SHOCT-domain-containing-protein
MTHLLPATPTEIFVYLLFSGISLYASWTVWGVVRVMMVERHVRKHGEAAEATVRELKDTGWRINKQPLFELLLDVRQSGRAAYQTKVKKKLGRHQSISTMGVGTRLDVKVDRNDPLKVAIVGAAMTAPVGAFMRQGMPSEGDPVKAMQNLQSLMDKGLITPEEFQAKKAQILARI
>NZ_CP017169.1|WP_140794187.1|6422648_6423422_+|alpha/beta-hydrolase
MGYVHILRGFASPHEGHSRTVRIYTPDTYDASPDRSFPVLYMQDGQNVFAHPESALFDTWCANLTLERLVAEHQVEPWLIVAVDSTHDRLSEYSPWDEPRSNVAARAEPYVRFMVETLKPYIERTYRVRKGPEWTAVMGASLGGLISLHLGQRHPALFGRIGGLSPSVMWSWNRMFSEWSAHSRRWTRIYLDAGTTETVDPVGYVMRYGEATRDFHRHLQSLGYADHELRLVLEPGGEHHERDWQRRLPEAMRWLLA
>NZ_CP017169.1|WP_140856101.1|6420866_6422480_-|sigma-54-interacting-transcriptional-regulator
MQQKLAADMSTTAGRAQAGQSPVALSVPALTIVSHPQPQRIGERLLLEVLASQGRTAALSRNAPDFSRPGGLMSLPLGDPFLSRKPVEFEPGPRGGLRMLVPEDGTQVRVANEPVMGGREFSREELSAGVPLVLADRVVLLLHLASSFRQPGVLDLGIVGHGEGIHRVREDIIRVADLTVPVLIRGETGTGKELVARAIHASGPRRAGPFVSVNLGALAKELVAAELFGAQRGAYTGASKDREGFFRAAEGGTLFLDEVGEAPPEVQAALLRVLETGEIYPVGGHTPVPVDVRLVSATDAHLEARIQERTFKAPLLHRLAGFEILVPPLRERREDVGLLFHHFARQELEAMGEGGQLTSSDPRAEPWLPAALAVQLVRHAWSGNIRQLRNVTRQLVIGSRGMPGLRADARLEQALDADAQPVPGRPLTERTGDEAGEGAKAPRRKPADVGEQELLEALRASSWDLKATADWLGIPRPSVYVLIDKSSLLRTARDLSPEEITRCFHECEGDLDRMVQRLEVSKRALQRRVRELGLSGG
>NZ_CP017169.1|WP_140856099.1|6420334_6420682_-|hypothetical-protein
MTVVTVTIKKSGDLVYEPNNKVRRGQPVRFVLDPLNGPLWATVNPPACLVATNSVTLDQTSAAPPIYEDPVSESAEFTTYSFTVEVPLLPEKPHFGGEAETKNGNLDVTTDPPKL
>NZ_CP017169.1|WP_140794181.1|6419799_6420219_-|hypothetical-protein
MVPANHRRQQFITRPSGAQEPRPMAIITVFINKSGNLSYIPNNKVRHGDTVRFAIDTVGSTSDVTVNPPACLDSTASFSLNNTSLAASQREDPVADGAAVGSYPFTVVTGGSPEARRHGLELETKNGNLDVTTDPPKEY
>NZ_CP017169.1|WP_140856097.1|6416122_6419794_+|protein-kinase
MHVAGRLNETYEEELLLAMDEGLLSGEEVAVLREEALRLRRGPLELLRERGRLSEDSLVALRGELASESTDPSAGRPLEAATLTPVTPGVSPPPAVEPDGATFPVPDWDRYQPVRFLGQGGMGRVFLAYDPMLRRNVALKFVRGDDPELARRFLSEARAQARVRHERVCEVYEVGEVRGRGYIAMRFVDGQPLGQLARSLTLEQKVLVLRQAAEGVHAAHGAGLIHRDIKPGNILVERTEDGGLAPFVMDFGLARDWREDGATPNAVQGTPHYMAPEQARGEVSRLDRRADIYALGATLYSLLTGRPPFTGATEAEVITRLQHEEPAPPRALDADIPSDLEAIVLKCLEKQRPARYDSARALAEDLERFLEGEPVLARQGLGYRLRRKARKHRVALTLGSAALTVVLLALIQAGIARGEVAERERLTRRFTERVERIEASARYSALSRLHDTREDRRELRASMDALEAEVREAGPHALGPGQYALGRALLVLDERDAARKRLEAAWAQGYREPRVAWALAQVLGDLYQERLLLDVERRSPEQREVRRKELEQNYRDPALAYLRQAEGPDVPVPPLYVKALFAFYEGRHEEALTHLEAMGRAQPWFYEAPLLQGDVLLARATQRWHQGDKAGSQEDLDAGRRAYAAAVATAESQPMGHYVLARLELAALVMELYGEGNVLPHYERGVEAATRALAAAPDHHRSLVVLSRLHRRLAEQRTSQGREDAEPLLEKSIHAAREALALAPPSDRVALELAITHRLSARYRQERGQDPSEQLRLSIEAFERLRPEERDYAFHANLGLTYQVWADAETERGVDPLEHQGKAIDAYLEAIRVRENQADAWINLGNALRRRASNPRATDAAGDLTRARDALAKALALNPGNVVASFRGAEISEQLARWRWSHGEPFEADLEQALALFRQGLGINAKLPPLHNGLGAALLWQAEQRWEEGGAPEPLLQQAQAAFEEARTLAPRQVYAHNNLGEVWTLNATFQSARRENPEPSGRTAVEAYRQALSLQPQDADLWANLGRVQTLLATWSVETGGDPRAELAKAEESLAQATTLNPRQGHTWRNTGEARALKARWLAHRGTAQESDFELASQAFQQALSLEPRRHDYRLATARFQLAWAAWRQQRNEDAAPLLNQGLALVAEVLADRPRWARAQALRGGGLLALAETRASSEQRQAWRIEGQEVLRQALARNPHLESEWRGRLGAAREPLAGPPTP
>NZ_CP017169.1|WP_140856110.1|6434946_6435900_+|IF-2-protein
MCGASVCSGVGVYPRAGAPQVKRRGRKWASRSYVRRAGDMNGTAQQGFGYRARRTFTRLLIFTLILGLGGVVVFLLSQLNARTFTLALHDGQLVVMKGRNAPMGAVPYRTGDPRLADAYAPVAIEGQDVSALLTRKFTDRDELDQALFPVLEGLARPRIASDEPARVDQGLYYLRRAEKLSGITEEQRLTLQKHMVDVAYYQARQKLEDARRLVSEALTQLKLAAESQSRHARSANQMLSAVAPPARELEDSLRRAVHTLSGPQVAPQTPPQAAPQPAPTAPPPAPTPQPETTGEALDEAPQAPTGTDAGGVVPTPP
>NZ_CP017169.1|WP_140856113.1|6436338_6438855_+|ribonucleoside-diphosphate-reductase-subunit-alpha
MNFDTPVKPSANMSVPPVSSGPSTPATTPAPTGAAASGAVASEPTAGDFSATSMRVRKRNGGAETVDLNKIVRAVGRSCVGLPRVDAMRVATKTISGLYDGATTRELDSLSIQTAAALIVEEPEYGRLSARLLATFIQKEVSNQDIHSFSQSVAAGHKHGLIADRLLQFVQANARKLNAAIDPSRNDLFEYFGLRTVYDRYLLKNPQTREVLETPQEFFLRVASALSGDNVNEAIELYRLFSSLEYLPSSPTLFNSGTRHEQLSSCFLLDSPADELDAIYKKYSDIAMLSKFSGGIGVAYHRVRARGSLIKSTNGHSNGIVPWLKTLDASVAAVNQGGKRKGACCVYLETWHADIEDFLELRENTGDDARRTHNLNLANWVPDLFMKRVEADGDWSLFDPKGVPHLTDLYGDAFEQAYAKAEADGLAMRKVKARDLYARMMKCLAQTGNGWMTFKDISNRKSNQTGKDGNVIHLSNLCTEILEVTSQGETAVCNLGSLNLSRMLVNGKFDFERLRANAQLAMRQLDRVIDLNYYPIPTAASSNKRWRPVGLGLMGLQDVFFQLKLAFDSAEARALSKKISEEIYFAALTTSCELAEQYGAHESFAETRAAKGELQFDHWGVVPEDTARWDALRQRIMKHGLRNSLMIAIAPTATIASIVGCYECIEPQVSNLFKRETLSGDFLQVNRYLVRDLQALGLWNENIRNRIKMAEGSVQDITELPENLRAVYRTAWELPMRSLLDMGADRGAFIDQSQSLNLFVETPNIGKLSSMYFYAWQKGLKTTYYLRSRPATRIAKATVGAGGGASMASAAPAPVAKATEAEAVACSLENPEACEACQ
>NZ_CP017169.1|WP_140856115.1|6438931_6439942_+|ribonucleotide-diphosphate-reductase-subunit-beta
MLLNPGLNLTLRPMAYPQFFEMYRNAIKNTWTVEEVDFSTDLVDLRSKMTDAERHLIHRLVAFFATGDSIVGNNLVLNLYKHLNAPEARMYLSRQLYEEALHVQFYLTLLDTYVPDPAERAMAFAAVDNIPSIQRKAQFCMKWMDSIQGMDTLQTKQDRRQFLLNLICFAGCIEGLFFFAAFAYVYFLRSKGLLNGLAAGTNWVFRDESAHMGFAFEAIQVARKEEPDLFDAQMERDVVAMLREAVECETQFAQDLLSGGVMGLSVQDMRGYLEYVADQRLQMLGMSPVFGTKNPLHFMDLQDVQELTNFFERRVSSYQVAVGVGAATDVVLDAAF
>NZ_CP017169.1|WP_140856118.1|6440080_6441127_+|DUF2169-domain-containing-protein
MGHPRIENETPFVFEPLPLADEEMRPLLTLVVKATFDVKAGQEPTLAPEQVPLQLAGKRWEGSELASYRYEPEAAFFKPATDVALVGHAHASQSGQRELVVSLQVGPVQKSVRVLGDRVWVKSLSSISMTQPIPFETIPLQYERAFGGWDRSHPEPAHHAFDARNPIGRGFRARHSRFEEGLRLPNLEEPLDPIRSWGQRPAPAGFGFLSPEWQPRASFAGTYDSRWNQARKPLLPADFDRRFFNAAAPALIAPAYLNGTEPITVINACAAGRLGFKLPGLPPPQVLISRLREPDTELRLNLDTVIIDTDAMHLMLIWRGMMALRRDPTEVTALRVTQDGAEKLTHLH
>NZ_CP017169.1|WP_140856120.1|6441172_6441637_+|DUF4150-domain-containing-protein
MATSVGVNKLSVVHKDTNGTTIAFPDICKTPNPAGPVPIPYPNIARSSDTAKGSKKVSVDGKPVCLKDSNFSTSTGDEAGTAGGGVASSKTKGKAEFVNYSFDVLFEGKNVARSFDLMLHNDKNTPPFPLLQGPVVAMGGSPSKPPCSECGEHY
>NZ_CP017169.1|WP_140858472.1|6441754_6442189_+|hypothetical-protein
MVRVGPGRQVWVDYPGNPRGALLARTSPTMELERLRQAASGPTEVLLAFADGVPTQPVLLTLLEPRTEAPLTEAILAQPLSRVPSEARVDGERVVITGRKEVVLECGKASLTLRRDGTVVLRGLNLVSEADEVHRIRGRKVRIN
>NZ_CP017169.1|WP_161606787.1|6442217_6443099_+|AHH-domain-containing-protein
MSEKQHTEDDKNLPGRHKKAGGVEGGACLNRHVPKVERKNSCSHRWQAYQRAKEDTALYNWPAYQSLSKPGGRIRTAASVDKRGNRFPDWYDFTIAAPSQLNGAPGRGTWDLDHGDNFQVKCYRPYWHEANHIIPNSSLRKVMADVGKGMSNPGRIALAVRGRLLNAQYNLNHKVNMILLPMDAEVAEALQLPRHRQTAFLCSHKAYSDNVEAELKTLFDALVKEPIRNHTVPKYNDCKDGLEALSQRLYKAIVAAGKRGTAALDNMASKDFKQPASTTASKPPSKPGSGKRP
>NZ_CP017169.1|WP_161606788.1|6443126_6443726_+|hypothetical-protein
MKFFNIETLGDPNDESLCMLHDVVERTERDSWRYKKGERLHPVYPPDAKLFMSRESRGIKLSDLIGNTEGMLIVSKAFREAIERHCQGVDIEYLPFTLYDHRKRVHSQDYCIINPIGSLDCLDEAASEVRYGSEGSVIDLGELVLDRTKVENAPQLFRMKQRPNKYVVGVELAREIYDQDFTNILWSELRFSDGADAPT
>NZ_CP017169.1|WP_161606789.1|6443739_6445098_+|TIGR02270-family-protein
MTVTPIPVPRRPAIVWSVVDEHLSEASFLWGQWERLLDATDHSFAEVLDDDEPRLLAHLEGLSVGGPPVAHKRLLPLLEGGEELRTVCAAAHALLDASDRDWLGVVLERLNDDDDALRQGLLRALELNERPDISTALLQQLPEASPVLQTGIMAVLRHRHTHPGDALSRMDRATSNVSAAAVRAATFAPLPLVSEFVWRGLTSGDASVRLAALETGLRRGLPIAWQACRAASEANGPEVRLGLLALSVGGTARDLKHVVAALDKPSIQTEALWALGFSGKLAAADALFSVLQAEPSPLAAESFSAITGLPLHPPFVNDTGEDTEPGPTDASIEAGGAPTVAVECVLPPPASGAGHVDTGKVEQWWSHARGRFDAASRYLYGHPYSVQALLSATERVPMRRRAAMALEIAIRSQGHCLIEPRLWATTQHRQAQELRKVRPRNLVVAFEALQAS
>NZ_CP017169.1|WP_161606790.1|6446221_6446983_+|immunity-49-family-protein
MNSEFLPVFVRNALADARRLLPSLEKSQVAQAQALEFCSHLRHAGIGTLFMTATPEVLHLRLKQSGEAFAWFLRGANEHAKQTGAARPFFDAVAAGDMEVAREVAKHARRTPAHGEEYEEDFLFIEFLMQRYLLGAESAACERLLARHEHVLQGAEDTRLPLCRALLVRDAEMFDDALTQFLQEREDAFEANAAGEPPERLATEGLFSVEGMALIRLAMLEGIPVAENHLHVPGVALEGSAPISGKDTWRHLD

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Crispr_ID: NZ_CP017169_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_11

6430044-6430254

Orphan

Consensus_repeat	Method
GCTTCCGCGAGCTGCGCTTCGAGTTCGG	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP017169_11

>merge|NZ_CP017169|11|6430044-6430254|CRISPRCasFinder
GCTTCCGCGAGCTGCGCTTCGAGTTCGGAGCGCTGGGCGTTGGAACGCGCGACGGCTTCCGCGAGCTGCGCTTCAAGTTCGGCGCGCTGAGCATCAGAACGCGTGACGGCGTCCGCGAGCTTCCCTTCGAGTTGGGCGCGCTGGGCCTCCAGCTCGCTACGGGCGCGCGTCAGTCCATCGGCTGAGTCCGTGAGCTGGGCCTCCAGCGCGT

>NZ_CP017169|11|10|6430044-6430254|CRISPRCasFinder
GCTTCCGCGAGCTGCGCTTCGAGTTCGG	AGCGCTGGGCGTTGGAACGCGCGACG
GCTTCCGCGAGCTGCGCTTCAAGTTCGG	CGCGCTGAGCATCAGAACGCGTGACG
GCGTCCGCGAGCTTCCCTTCGAGTTGGG	CGCGCTGGGCCTCCAGCTCGCTACGGGCGCGCGTCAGTCCATCGGCT
GAGTCCGTGAGCTGGGCCTCCAGCGCGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140856115.1\|6438931_6439942_+\|ribonucleotide-diphosphate-reductase-subunit-beta	unknown	unknown	gnl\|CDD\|153108
NZ_CP017169.1\|WP_140794192.1\|6426086_6427937_-\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017169.1\|WP_140856110.1\|6434946_6435900_+\|IF-2-protein	unknown	unknown	gnl\|CDD\|237057
NZ_CP017169.1\|WP_161606787.1\|6442217_6443099_+\|AHH-domain-containing-protein	unknown	unknown	gnl\|CDD\|379603
NZ_CP017169.1\|WP_140794193.1\|6427975_6428827_-\|diaminopimelate-epimerase	unknown	unknown	gnl\|CDD\|234768
NZ_CP017169.1\|WP_140856120.1\|6441172_6441637_+\|DUF4150-domain-containing-protein	unknown	unknown	gnl\|CDD\|372665
NZ_CP017169.1\|WP_140794187.1\|6422648_6423422_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225375
NZ_CP017169.1\|WP_140858472.1\|6441754_6442189_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140856101.1\|6420866_6422480_-\|sigma-54-interacting-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017169.1\|WP_140794181.1\|6419799_6420219_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_161606789.1\|6443739_6445098_+\|TIGR02270-family-protein	unknown	unknown	gnl\|CDD\|131323
NZ_CP017169.1\|WP_140856099.1\|6420334_6420682_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_161606790.1\|6446221_6446983_+\|immunity-49-family-protein	unknown	unknown	gnl\|CDD\|373949
NZ_CP017169.1\|WP_140856113.1\|6436338_6438855_+\|ribonucleoside-diphosphate-reductase-subunit-alpha	unknown	unknown	gnl\|CDD\|178056
NZ_CP017169.1\|WP_140856118.1\|6440080_6441127_+\|DUF2169-domain-containing-protein	unknown	unknown	gnl\|CDD\|370755
NZ_CP017169.1\|WP_140799406.1\|6424567_6426067_-\|DUF4388-domain-containing-protein	unknown	unknown	gnl\|CDD\|373017
NZ_CP017169.1\|WP_161606788.1\|6443126_6443726_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140856104.1\|6423472_6424000_+\|SHOCT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378276
NZ_CP017169.1\|WP_140856106.1\|6424021_6424555_+\|SHOCT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378822
NZ_CP017169.1\|WP_140856097.1\|6416122_6419794_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140856115.1\|6438931_6439942_+\|ribonucleotide-diphosphate-reductase-subunit-beta	gnl\|CDD\|153108	cd01049, RNRR2, Ribonucleotide Reductase, R2/beta subunit, ferritin-like diiron-binding domain. Ribonucleotide Reductase, R2/beta subunit (RNRR2) is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. The RNR protein catalyzes the conversion of ribonucleotides to deoxyribonucleotides and is found in all eukaryotes, many prokaryotes, several viruses, and few archaea. The catalytically active form of RNR is a proposed alpha2-beta2 tetramer. The homodimeric alpha subunit (R1) contains the active site and redox active cysteines as well as the allosteric binding sites. The beta subunit (R2) contains a diiron cluster that, in its reduced state, reacts with dioxygen to form a stable tyrosyl radical and a diiron(III) cluster. This essential tyrosyl radical is proposed to generate a thiyl radical, located on a cysteine residue in the R1 active site that initiates ribonucleotide reduction. The beta subunit is composed of 10-13 helices, the 8 longest helices form an alpha-helical bundle; some have 2 addition beta strands. Yeast is unique in that it assembles both homodimers and heterodimers of RNRR2. The yeast heterodimer, Y2Y4, contains R2 (Y2) and a R2 homolog (Y4) that lacks the diiron center and is proposed to only assist in cofactor assembly, and perhaps stabilize R1 (Y1) in its active conformation.	2.13152e-103
NZ_CP017169.1\|WP_140794192.1\|6426086_6427937_-\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	2.45621e-27
NZ_CP017169.1\|WP_140856110.1\|6434946_6435900_+\|IF-2-protein	gnl\|CDD\|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	0.000317524
NZ_CP017169.1\|WP_161606787.1\|6442217_6443099_+\|AHH-domain-containing-protein	gnl\|CDD\|379603	pfam14412, AHH, A nuclease family of the HNH/ENDO VII superfamily with conserved AHH. AHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif, AHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. Like WHH and LHH, the AHH nuclease contains 4 conserved histidines of which, the first one is predicted to bind a metal-ion and the other three ones are involved in activation of a water molecule for hydrolysis.	0.00603012
NZ_CP017169.1\|WP_140794193.1\|6427975_6428827_-\|diaminopimelate-epimerase	gnl\|CDD\|234768	PRK00450, dapF, diaminopimelate epimerase; Provisional.	1.52191e-97
NZ_CP017169.1\|WP_140856120.1\|6441172_6441637_+\|DUF4150-domain-containing-protein	gnl\|CDD\|372665	pfam13665, DUF4150, Domain of unknown function (DUF4150).	1.70847e-47
NZ_CP017169.1\|WP_140856101.1\|6420866_6422480_-\|sigma-54-interacting-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	7.34556e-92
NZ_CP017169.1\|WP_161606789.1\|6443739_6445098_+\|TIGR02270-family-protein	gnl\|CDD\|131323	TIGR02270, hypothetical_protein_GSU3180, conserved hypothetical protein. Members are found in Myxococcus xanthus (six members), Geobacter sulfurreducens, and Pseudomonas aeruginosa; a short protein homologous to the N-terminal region is found in Mesorhizobium loti. All sequence are from Proteobacteria. The function is unknown. [Hypothetical proteins, Conserved].	2.37233e-53
NZ_CP017169.1\|WP_140794187.1\|6422648_6423422_+\|alpha/beta-hydrolase	gnl\|CDD\|225375	COG2819, COG2819, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	1.13889e-34
NZ_CP017169.1\|WP_161606790.1\|6446221_6446983_+\|immunity-49-family-protein	gnl\|CDD\|373949	pfam15575, Imm49, Immunity protein 49. A predicted immunity protein with an all alpha-helical fold and a conserved proline residue. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REAse-1 or Tox-REase-6 families.	1.3404e-08
NZ_CP017169.1\|WP_140856113.1\|6436338_6438855_+\|ribonucleoside-diphosphate-reductase-subunit-alpha	gnl\|CDD\|178056	PLN02437, PLN02437, ribonucleoside--diphosphate reductase large subunit.	0
NZ_CP017169.1\|WP_140856118.1\|6440080_6441127_+\|DUF2169-domain-containing-protein	gnl\|CDD\|370755	pfam09937, DUF2169, Uncharacterized protein conserved in bacteria (DUF2169). This domain, found in various hypothetical prokaryotic proteins, has no known function.	5.50692e-109
NZ_CP017169.1\|WP_140799406.1\|6424567_6426067_-\|DUF4388-domain-containing-protein	gnl\|CDD\|373017	pfam14332, DUF4388, Domain of unknown function (DUF4388). This domain family is found in bacteria, and is typically between 102 and 135 amino acids in length.	8.86263e-29
NZ_CP017169.1\|WP_140856104.1\|6423472_6424000_+\|SHOCT-domain-containing-protein	gnl\|CDD\|378276	pfam09851, SHOCT, Short C-terminal domain.	2.23681e-06
NZ_CP017169.1\|WP_140856106.1\|6424021_6424555_+\|SHOCT-domain-containing-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.	1.34026e-05
NZ_CP017169.1\|WP_140856097.1\|6416122_6419794_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	9.38282e-89

>NZ_CP017169.1|WP_140794193.1|6427975_6428827_-|diaminopimelate-epimerase
MEARERIFKYQGLGNDFVVLDRRGSGEDIDAATSRWMCDRRLGIGGDGVLALLPSERGVARMVVHNADGSIAEMCGNGLRCAVKFLVDDSGQTPGHLDVETGAGVLTCYPSYGEGGVVAVDISMGPARLVAPNLPSGVTGQPFLDAFVPGHPHLRAYAVSMGNPHMVLLDQPLEDASRLGPLLERHPSFPDRTNVEFVRVDSDGLTVVVWERGCGLTQACGTGACASAVAAVLAKRLPADAWLRVTLPGGDLRIRVPADLSDIRLRGPVAFVFEGVVAVPSGR
>NZ_CP017169.1|WP_140794192.1|6426086_6427937_-|response-regulator
MAGPILVVDDDLFFRQLASDLLTHNGHRVVAVENATLALEEAARTPFDLVITDVVMPGVDGFALTARLRERDPDQEVILVSHRTDIRNSEVALRSGAADCLTKPVDANDMLLAVDRALERASLRRERTQLRDENLEFARFHNLHQRCLELLSHPDLEWLQERLTSELAAICDAQSAALWVVDDRGDLVLRAYRGLLDRQFLAEKMSPEGPLSGRLREAQPWLARDERSSVMYVPLVASGEVVGLAQLSDPLSGDFRPEHSRDARVLGDFAAVGLKNGRKMLALQRLGLRDRETAAYNLSYFTDYASKEIYKARRYGRTFSLLTFSIDNLPLVRVRQGAADAKKAVRGIIKALSKIIRDSDVIAKASDQEFYLLLPETDFFGALMFVRRAVAAVREEPEAMEVDQRLPLAMVGGASTFPKDGEDFDELVHRCRRRMDERRASLQRRLMLDGLPFWDEVDLLLGTPNSPRLPVDERSEPSRRGKVSDVLFDELQAEIAREMMRDPGSRGLLYVGGPEIRTDLNIAAGLESAPPDLASRIYLLGRRVDLESHPALTPVFLEGDDRIARHEFILWLSENAAYALIQRRGHGATWGFHTSDTAVVDGLISKLQAEYDLQPY
>NZ_CP017169.1|WP_140799406.1|6424567_6426067_-|DUF4388-domain-containing-protein
MAPVRKILIADPDLESVRSLSRALRTKGYQVHYAPDGSRALEVAVLRHPDLTLFDEGCRLLDARTFIQILRTNPRTEDIPVVLTTASFESDRLRGLRDGYLRKPFNLDEVLSRIEHIFRRSEAAKDLKSEQQEIEGSLSQLSIPDLMQLLGMNRRSGRLTLERGNDRGEISVVEGRPVNAKLGRVEGEKALFRLLAWVDGTFTFSPGGNTARPRINRGMDDALLEGMRQSDEVNRLMPGLPPRHTRLMLAPDADLQGDQHPVTQQVVDLLRHPRALGEVLDLAPATDLEVLNVLTTLMQRGVAKAADGDGVEAASGELLGAAEVHALRGRILRTRAPAKVATAKIFVCGSGASAARRVLSRMPGMEALSADPTAVKSGFGTLGRLVLSEVLRLDFCVLPPAEAARPLWRPFTAGAMGALLMDVAEPSVRLARYLAWEVRMPVVVVGAEVPAALQGAPAGALGAADDLADALRSLLVQALNPAPTLPGVPQVQRAAASIV
>NZ_CP017169.1|WP_140856106.1|6424021_6424555_+|SHOCT-domain-containing-protein
MLTAVLAMLPFLLFSLVGFGVAGYFFYAHAQTQRLREHGTAGEATILRMERTSMRINKSYVYDFLLEFKVPGLPTYRRQHRSRAHDWKAFILEPGVRLKVKIDPNDPQRFVVLGPVDEQRPQIIQALIAGAAGFSESRTVAPSDPVKALKDLQSMLDNELITQDEYARKKAEILSRL
>NZ_CP017169.1|WP_140856104.1|6423472_6424000_+|SHOCT-domain-containing-protein
MTHLLPATPTEIFVYLLFSGISLYASWTVWGVVRVMMVERHVRKHGEAAEATVRELKDTGWRINKQPLFELLLDVRQSGRAAYQTKVKKKLGRHQSISTMGVGTRLDVKVDRNDPLKVAIVGAAMTAPVGAFMRQGMPSEGDPVKAMQNLQSLMDKGLITPEEFQAKKAQILARI
>NZ_CP017169.1|WP_140794187.1|6422648_6423422_+|alpha/beta-hydrolase
MGYVHILRGFASPHEGHSRTVRIYTPDTYDASPDRSFPVLYMQDGQNVFAHPESALFDTWCANLTLERLVAEHQVEPWLIVAVDSTHDRLSEYSPWDEPRSNVAARAEPYVRFMVETLKPYIERTYRVRKGPEWTAVMGASLGGLISLHLGQRHPALFGRIGGLSPSVMWSWNRMFSEWSAHSRRWTRIYLDAGTTETVDPVGYVMRYGEATRDFHRHLQSLGYADHELRLVLEPGGEHHERDWQRRLPEAMRWLLA
>NZ_CP017169.1|WP_140856101.1|6420866_6422480_-|sigma-54-interacting-transcriptional-regulator
MQQKLAADMSTTAGRAQAGQSPVALSVPALTIVSHPQPQRIGERLLLEVLASQGRTAALSRNAPDFSRPGGLMSLPLGDPFLSRKPVEFEPGPRGGLRMLVPEDGTQVRVANEPVMGGREFSREELSAGVPLVLADRVVLLLHLASSFRQPGVLDLGIVGHGEGIHRVREDIIRVADLTVPVLIRGETGTGKELVARAIHASGPRRAGPFVSVNLGALAKELVAAELFGAQRGAYTGASKDREGFFRAAEGGTLFLDEVGEAPPEVQAALLRVLETGEIYPVGGHTPVPVDVRLVSATDAHLEARIQERTFKAPLLHRLAGFEILVPPLRERREDVGLLFHHFARQELEAMGEGGQLTSSDPRAEPWLPAALAVQLVRHAWSGNIRQLRNVTRQLVIGSRGMPGLRADARLEQALDADAQPVPGRPLTERTGDEAGEGAKAPRRKPADVGEQELLEALRASSWDLKATADWLGIPRPSVYVLIDKSSLLRTARDLSPEEITRCFHECEGDLDRMVQRLEVSKRALQRRVRELGLSGG
>NZ_CP017169.1|WP_140856099.1|6420334_6420682_-|hypothetical-protein
MTVVTVTIKKSGDLVYEPNNKVRRGQPVRFVLDPLNGPLWATVNPPACLVATNSVTLDQTSAAPPIYEDPVSESAEFTTYSFTVEVPLLPEKPHFGGEAETKNGNLDVTTDPPKL
>NZ_CP017169.1|WP_140794181.1|6419799_6420219_-|hypothetical-protein
MVPANHRRQQFITRPSGAQEPRPMAIITVFINKSGNLSYIPNNKVRHGDTVRFAIDTVGSTSDVTVNPPACLDSTASFSLNNTSLAASQREDPVADGAAVGSYPFTVVTGGSPEARRHGLELETKNGNLDVTTDPPKEY
>NZ_CP017169.1|WP_140856097.1|6416122_6419794_+|protein-kinase
MHVAGRLNETYEEELLLAMDEGLLSGEEVAVLREEALRLRRGPLELLRERGRLSEDSLVALRGELASESTDPSAGRPLEAATLTPVTPGVSPPPAVEPDGATFPVPDWDRYQPVRFLGQGGMGRVFLAYDPMLRRNVALKFVRGDDPELARRFLSEARAQARVRHERVCEVYEVGEVRGRGYIAMRFVDGQPLGQLARSLTLEQKVLVLRQAAEGVHAAHGAGLIHRDIKPGNILVERTEDGGLAPFVMDFGLARDWREDGATPNAVQGTPHYMAPEQARGEVSRLDRRADIYALGATLYSLLTGRPPFTGATEAEVITRLQHEEPAPPRALDADIPSDLEAIVLKCLEKQRPARYDSARALAEDLERFLEGEPVLARQGLGYRLRRKARKHRVALTLGSAALTVVLLALIQAGIARGEVAERERLTRRFTERVERIEASARYSALSRLHDTREDRRELRASMDALEAEVREAGPHALGPGQYALGRALLVLDERDAARKRLEAAWAQGYREPRVAWALAQVLGDLYQERLLLDVERRSPEQREVRRKELEQNYRDPALAYLRQAEGPDVPVPPLYVKALFAFYEGRHEEALTHLEAMGRAQPWFYEAPLLQGDVLLARATQRWHQGDKAGSQEDLDAGRRAYAAAVATAESQPMGHYVLARLELAALVMELYGEGNVLPHYERGVEAATRALAAAPDHHRSLVVLSRLHRRLAEQRTSQGREDAEPLLEKSIHAAREALALAPPSDRVALELAITHRLSARYRQERGQDPSEQLRLSIEAFERLRPEERDYAFHANLGLTYQVWADAETERGVDPLEHQGKAIDAYLEAIRVRENQADAWINLGNALRRRASNPRATDAAGDLTRARDALAKALALNPGNVVASFRGAEISEQLARWRWSHGEPFEADLEQALALFRQGLGINAKLPPLHNGLGAALLWQAEQRWEEGGAPEPLLQQAQAAFEEARTLAPRQVYAHNNLGEVWTLNATFQSARRENPEPSGRTAVEAYRQALSLQPQDADLWANLGRVQTLLATWSVETGGDPRAELAKAEESLAQATTLNPRQGHTWRNTGEARALKARWLAHRGTAQESDFELASQAFQQALSLEPRRHDYRLATARFQLAWAAWRQQRNEDAAPLLNQGLALVAEVLADRPRWARAQALRGGGLLALAETRASSEQRQAWRIEGQEVLRQALARNPHLESEWRGRLGAAREPLAGPPTP
>NZ_CP017169.1|WP_140856110.1|6434946_6435900_+|IF-2-protein
MCGASVCSGVGVYPRAGAPQVKRRGRKWASRSYVRRAGDMNGTAQQGFGYRARRTFTRLLIFTLILGLGGVVVFLLSQLNARTFTLALHDGQLVVMKGRNAPMGAVPYRTGDPRLADAYAPVAIEGQDVSALLTRKFTDRDELDQALFPVLEGLARPRIASDEPARVDQGLYYLRRAEKLSGITEEQRLTLQKHMVDVAYYQARQKLEDARRLVSEALTQLKLAAESQSRHARSANQMLSAVAPPARELEDSLRRAVHTLSGPQVAPQTPPQAAPQPAPTAPPPAPTPQPETTGEALDEAPQAPTGTDAGGVVPTPP
>NZ_CP017169.1|WP_140856113.1|6436338_6438855_+|ribonucleoside-diphosphate-reductase-subunit-alpha
MNFDTPVKPSANMSVPPVSSGPSTPATTPAPTGAAASGAVASEPTAGDFSATSMRVRKRNGGAETVDLNKIVRAVGRSCVGLPRVDAMRVATKTISGLYDGATTRELDSLSIQTAAALIVEEPEYGRLSARLLATFIQKEVSNQDIHSFSQSVAAGHKHGLIADRLLQFVQANARKLNAAIDPSRNDLFEYFGLRTVYDRYLLKNPQTREVLETPQEFFLRVASALSGDNVNEAIELYRLFSSLEYLPSSPTLFNSGTRHEQLSSCFLLDSPADELDAIYKKYSDIAMLSKFSGGIGVAYHRVRARGSLIKSTNGHSNGIVPWLKTLDASVAAVNQGGKRKGACCVYLETWHADIEDFLELRENTGDDARRTHNLNLANWVPDLFMKRVEADGDWSLFDPKGVPHLTDLYGDAFEQAYAKAEADGLAMRKVKARDLYARMMKCLAQTGNGWMTFKDISNRKSNQTGKDGNVIHLSNLCTEILEVTSQGETAVCNLGSLNLSRMLVNGKFDFERLRANAQLAMRQLDRVIDLNYYPIPTAASSNKRWRPVGLGLMGLQDVFFQLKLAFDSAEARALSKKISEEIYFAALTTSCELAEQYGAHESFAETRAAKGELQFDHWGVVPEDTARWDALRQRIMKHGLRNSLMIAIAPTATIASIVGCYECIEPQVSNLFKRETLSGDFLQVNRYLVRDLQALGLWNENIRNRIKMAEGSVQDITELPENLRAVYRTAWELPMRSLLDMGADRGAFIDQSQSLNLFVETPNIGKLSSMYFYAWQKGLKTTYYLRSRPATRIAKATVGAGGGASMASAAPAPVAKATEAEAVACSLENPEACEACQ
>NZ_CP017169.1|WP_140856115.1|6438931_6439942_+|ribonucleotide-diphosphate-reductase-subunit-beta
MLLNPGLNLTLRPMAYPQFFEMYRNAIKNTWTVEEVDFSTDLVDLRSKMTDAERHLIHRLVAFFATGDSIVGNNLVLNLYKHLNAPEARMYLSRQLYEEALHVQFYLTLLDTYVPDPAERAMAFAAVDNIPSIQRKAQFCMKWMDSIQGMDTLQTKQDRRQFLLNLICFAGCIEGLFFFAAFAYVYFLRSKGLLNGLAAGTNWVFRDESAHMGFAFEAIQVARKEEPDLFDAQMERDVVAMLREAVECETQFAQDLLSGGVMGLSVQDMRGYLEYVADQRLQMLGMSPVFGTKNPLHFMDLQDVQELTNFFERRVSSYQVAVGVGAATDVVLDAAF
>NZ_CP017169.1|WP_140856118.1|6440080_6441127_+|DUF2169-domain-containing-protein
MGHPRIENETPFVFEPLPLADEEMRPLLTLVVKATFDVKAGQEPTLAPEQVPLQLAGKRWEGSELASYRYEPEAAFFKPATDVALVGHAHASQSGQRELVVSLQVGPVQKSVRVLGDRVWVKSLSSISMTQPIPFETIPLQYERAFGGWDRSHPEPAHHAFDARNPIGRGFRARHSRFEEGLRLPNLEEPLDPIRSWGQRPAPAGFGFLSPEWQPRASFAGTYDSRWNQARKPLLPADFDRRFFNAAAPALIAPAYLNGTEPITVINACAAGRLGFKLPGLPPPQVLISRLREPDTELRLNLDTVIIDTDAMHLMLIWRGMMALRRDPTEVTALRVTQDGAEKLTHLH
>NZ_CP017169.1|WP_140856120.1|6441172_6441637_+|DUF4150-domain-containing-protein
MATSVGVNKLSVVHKDTNGTTIAFPDICKTPNPAGPVPIPYPNIARSSDTAKGSKKVSVDGKPVCLKDSNFSTSTGDEAGTAGGGVASSKTKGKAEFVNYSFDVLFEGKNVARSFDLMLHNDKNTPPFPLLQGPVVAMGGSPSKPPCSECGEHY
>NZ_CP017169.1|WP_140858472.1|6441754_6442189_+|hypothetical-protein
MVRVGPGRQVWVDYPGNPRGALLARTSPTMELERLRQAASGPTEVLLAFADGVPTQPVLLTLLEPRTEAPLTEAILAQPLSRVPSEARVDGERVVITGRKEVVLECGKASLTLRRDGTVVLRGLNLVSEADEVHRIRGRKVRIN
>NZ_CP017169.1|WP_161606787.1|6442217_6443099_+|AHH-domain-containing-protein
MSEKQHTEDDKNLPGRHKKAGGVEGGACLNRHVPKVERKNSCSHRWQAYQRAKEDTALYNWPAYQSLSKPGGRIRTAASVDKRGNRFPDWYDFTIAAPSQLNGAPGRGTWDLDHGDNFQVKCYRPYWHEANHIIPNSSLRKVMADVGKGMSNPGRIALAVRGRLLNAQYNLNHKVNMILLPMDAEVAEALQLPRHRQTAFLCSHKAYSDNVEAELKTLFDALVKEPIRNHTVPKYNDCKDGLEALSQRLYKAIVAAGKRGTAALDNMASKDFKQPASTTASKPPSKPGSGKRP
>NZ_CP017169.1|WP_161606788.1|6443126_6443726_+|hypothetical-protein
MKFFNIETLGDPNDESLCMLHDVVERTERDSWRYKKGERLHPVYPPDAKLFMSRESRGIKLSDLIGNTEGMLIVSKAFREAIERHCQGVDIEYLPFTLYDHRKRVHSQDYCIINPIGSLDCLDEAASEVRYGSEGSVIDLGELVLDRTKVENAPQLFRMKQRPNKYVVGVELAREIYDQDFTNILWSELRFSDGADAPT
>NZ_CP017169.1|WP_161606789.1|6443739_6445098_+|TIGR02270-family-protein
MTVTPIPVPRRPAIVWSVVDEHLSEASFLWGQWERLLDATDHSFAEVLDDDEPRLLAHLEGLSVGGPPVAHKRLLPLLEGGEELRTVCAAAHALLDASDRDWLGVVLERLNDDDDALRQGLLRALELNERPDISTALLQQLPEASPVLQTGIMAVLRHRHTHPGDALSRMDRATSNVSAAAVRAATFAPLPLVSEFVWRGLTSGDASVRLAALETGLRRGLPIAWQACRAASEANGPEVRLGLLALSVGGTARDLKHVVAALDKPSIQTEALWALGFSGKLAAADALFSVLQAEPSPLAAESFSAITGLPLHPPFVNDTGEDTEPGPTDASIEAGGAPTVAVECVLPPPASGAGHVDTGKVEQWWSHARGRFDAASRYLYGHPYSVQALLSATERVPMRRRAAMALEIAIRSQGHCLIEPRLWATTQHRQAQELRKVRPRNLVVAFEALQAS
>NZ_CP017169.1|WP_161606790.1|6446221_6446983_+|immunity-49-family-protein
MNSEFLPVFVRNALADARRLLPSLEKSQVAQAQALEFCSHLRHAGIGTLFMTATPEVLHLRLKQSGEAFAWFLRGANEHAKQTGAARPFFDAVAAGDMEVAREVAKHARRTPAHGEEYEEDFLFIEFLMQRYLLGAESAACERLLARHEHVLQGAEDTRLPLCRALLVRDAEMFDDALTQFLQEREDAFEANAAGEPPERLATEGLFSVEGMALIRLAMLEGIPVAENHLHVPGVALEGSAPISGKDTWRHLD

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Crispr_ID: NZ_CP017169_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_12

6769220-6769305

Orphan

Consensus_repeat	Method
TCGTCGAGCGGCGGCGGAGGGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017169_12

>merge|NZ_CP017169|12|6769220-6769305|CRISPRCasFinder
TCTTCGTCGAGCGGCGGCGGAGGGGGCATGCCCCGCGCATCCGCGCTCTCGACAGGTGCATCCACGTCGTCGAGCGGCGGCGGAGG

>NZ_CP017169|12|11|6769220-6769305|CRISPRCasFinder
TCTTCGTCGAGCGGCGGCGGAGG	GGGCATGCCCCGCGCATCCGCGCTCTCGACAGGTGCATCC
ACGTCGTCGAGCGGCGGCGGAGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140856387.1\|6766377_6767043_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140794438.1\|6756786_6757341_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237865
NZ_CP017169.1\|WP_140856380.1\|6758482_6760723_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340831
NZ_CP017169.1\|WP_140856394.1\|6780615_6782352_-\|DNA-repair-protein-RecN	unknown	unknown	gnl\|CDD\|223571
NZ_CP017169.1\|WP_140794446.1\|6769781_6770339_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP017169.1\|WP_140794450.1\|6773515_6776338_-\|preprotein-translocase-subunit-SecA	unknown	unknown	gnl\|CDD\|237259
NZ_CP017169.1\|WP_140856391.1\|6777753_6778458_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|128563
NZ_CP017169.1\|WP_140856389.1\|6772158_6773136_-\|30S-ribosomal-protein-S2	unknown	unknown	gnl\|CDD\|235396
NZ_CP017169.1\|WP_140794437.1\|6756261_6756783_+\|DUF1768-domain-containing-protein	unknown	unknown	gnl\|CDD\|378035
NZ_CP017169.1\|WP_140858502.1\|6757349_6758435_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340838
NZ_CP017169.1\|WP_140794448.1\|6771346_6772000_-\|translation-elongation-factor-Ts	unknown	unknown	gnl\|CDD\|183447
NZ_CP017169.1\|WP_140794453.1\|6778620_6779538_-\|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl\|CDD\|366703
NZ_CP017169.1\|WP_140856385.1\|6762575_6766355_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235832
NZ_CP017169.1\|WP_140856382.1\|6760719_6761442_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237030
NZ_CP017169.1\|WP_140799531.1\|6776688_6777711_+\|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	unknown	unknown	gnl\|CDD\|236971
NZ_CP017169.1\|WP_140794444.1\|6767743_6768076_+\|iron-donor-protein-CyaY	unknown	unknown	gnl\|CDD\|274572
NZ_CP017169.1\|WP_140794447.1\|6770377_6771130_-\|UMP-kinase	unknown	unknown	gnl\|CDD\|234735
NZ_CP017169.1\|WP_011555314.1\|6779757_6780555_-\|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP017169.1\|WP_140794443.1\|6767232_6767730_+\|histidine-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|224973
NZ_CP017169.1\|WP_140796619.1\|6761594_6762416_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133031

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140794438.1\|6756786_6757341_-\|hypothetical-protein	gnl\|CDD\|237865	PRK14951, PRK14951, DNA polymerase III subunits gamma and tau; Provisional.	0.000284644
NZ_CP017169.1\|WP_140856380.1\|6758482_6760723_+\|glycosyltransferase	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	4.59252e-31
NZ_CP017169.1\|WP_140856394.1\|6780615_6782352_-\|DNA-repair-protein-RecN	gnl\|CDD\|223571	COG0497, RecN, ATPase involved in DNA repair [DNA replication, recombination, and repair].	0
NZ_CP017169.1\|WP_140794446.1\|6769781_6770339_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	3.60497e-96
NZ_CP017169.1\|WP_140794450.1\|6773515_6776338_-\|preprotein-translocase-subunit-SecA	gnl\|CDD\|237259	PRK12904, PRK12904, preprotein translocase subunit SecA; Reviewed.	0
NZ_CP017169.1\|WP_140856391.1\|6777753_6778458_+\|diguanylate-cyclase	gnl\|CDD\|128563	smart00267, GGDEF, diguanylate cyclase. Diguanylate cyclase, present in a variety of bacteria.	5.51889e-05
NZ_CP017169.1\|WP_140856389.1\|6772158_6773136_-\|30S-ribosomal-protein-S2	gnl\|CDD\|235396	PRK05299, rpsB, 30S ribosomal protein S2; Provisional.	8.67253e-165
NZ_CP017169.1\|WP_140794437.1\|6756261_6756783_+\|DUF1768-domain-containing-protein	gnl\|CDD\|378035	pfam08719, DUF1768, Domain of unknown function (DUF1768). This is a domain of unknown function. It is alpha helical in structure. The GO annotation for this protein suggests it is involved in nematode larval development and has a positive regulation on growth rate.	7.38866e-78
NZ_CP017169.1\|WP_140858502.1\|6757349_6758435_-\|glycosyltransferase	gnl\|CDD\|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	4.26532e-98
NZ_CP017169.1\|WP_140794448.1\|6771346_6772000_-\|translation-elongation-factor-Ts	gnl\|CDD\|183447	PRK12332, tsf, elongation factor Ts; Reviewed.	1.11675e-104
NZ_CP017169.1\|WP_140794453.1\|6778620_6779538_-\|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl\|CDD\|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	1.65938e-47
NZ_CP017169.1\|WP_140856385.1\|6762575_6766355_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|235832	PRK06567, PRK06567, putative bifunctional glutamate synthase subunit beta/2-polyprenylphenol hydroxylase; Validated.	1.61572e-176
NZ_CP017169.1\|WP_140856382.1\|6760719_6761442_+\|hypothetical-protein	gnl\|CDD\|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.59701e-05
NZ_CP017169.1\|WP_140799531.1\|6776688_6777711_+\|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	gnl\|CDD\|236971	PRK11760, PRK11760, putative 23S rRNA C2498 ribose 2'-O-ribose methyltransferase; Provisional.	5.15127e-44
NZ_CP017169.1\|WP_140794444.1\|6767743_6768076_+\|iron-donor-protein-CyaY	gnl\|CDD\|274572	TIGR03421, FeS_CyaY, iron donor protein CyaY. Members of this protein family are the iron-sulfur cluster (FeS) metabolism protein CyaY, a homolog of eukaryotic frataxin. ISC is one of several bacterial systems for FeS assembly; we find by Partial Phylogenetic Profiling vs. the ISC system that CyaY most like work with the ISC system for FeS cluster biosynthesis. A study of of cyaY mutants in Salmonella enterica bears this out. Although the trusted cutoff is set low enough to include eukaryotic frataxin sequences, a narrower, exception-type model (TIGR03421) identifies identifies members of that specific set. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	1.13094e-33
NZ_CP017169.1\|WP_140796619.1\|6761594_6762416_+\|glycosyltransferase	gnl\|CDD\|133031	cd04188, DPG_synthase, DPG_synthase is involved in protein N-linked glycosylation. UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate.	8.1848e-76
NZ_CP017169.1\|WP_011555314.1\|6779757_6780555_-\|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	5.5045e-78
NZ_CP017169.1\|WP_140794443.1\|6767232_6767730_+\|histidine-phosphatase-family-protein	gnl\|CDD\|224973	COG2062, SixA, Phosphohistidine phosphatase SixA [Signal transduction mechanisms].	1.01793e-20
NZ_CP017169.1\|WP_140794447.1\|6770377_6771130_-\|UMP-kinase	gnl\|CDD\|234735	PRK00358, pyrH, uridylate kinase; Provisional.	7.49448e-150

>NZ_CP017169.1|WP_140794444.1|6767743_6768076_+|iron-donor-protein-CyaY
MMDEARYNQLVSAAFKRILAAADAIDPDILEADSTGDMVTLTAASREKCIVNTQRAVRQIWVAGRGQGIHFDYDAATGTWKDDKGRGLELMSFVADVVRGITGADFAYPG
>NZ_CP017169.1|WP_140794443.1|6767232_6767730_+|histidine-phosphatase-family-protein
MRLFLVRHADADAEIPEGLGDEARALTAKSRTSTAHHFASLTERIGPVGRILTSPLVRTVQTAQILSISAKFEGPLKVHRCLLPDMPVGAVEPVLNEYADENLVLVGHQPSMGALAAHLLGMQSFPKPVNPGTVIGLERAEGESSPPFKFLFYAAPGQQVLDIIQ
>NZ_CP017169.1|WP_140856387.1|6766377_6767043_-|hypothetical-protein
MRKVLWGLWVLVAFSACKKPEDASAPPAGAVGEQAPGAPAGVVEAGPYTVTKEKLDAYVGYQRRMLDVYGSLMKGLQNLGALVDAGTPEAMAAAREGLKVVEAKAKAEAEARREAQLSEADVNGIAEVVTAVISQRQLGRTLQYEEELKKLESLQAKLPPEQQQGMAPQVASMRAQVEAFQTLADARRDYGDANVDVVLTREEDLIQNYQEMIRVFTGTRR
>NZ_CP017169.1|WP_140856385.1|6762575_6766355_+|FAD-dependent-oxidoreductase
MRALTDLPSDPTPPLTLGLPGFVFEDLYRPAGLRRLAERFDAQLAEDEPELFHAFDAYRKSGGKSVSGAAESDLLIRVSRHVSRFVTRLFRVEQELERMAGRLKGELPLFDFKREFITRRVFKKGAADRPALAEFPSLDARMRLMLQLGFPEALATGDLERGLAESVLALMDLERLFSNALPAERQGEAEALRARWSALREVLLSTPEGKDAFGSSLVTQGDDAAELQSVRALLSLADRWTYARALHPETKDIFHAWPTHRIPKPLVFDQLVHLQRPDNELPEATEGLEHHLRHRDGFKLTDRRGTSRDVMNEVDYCVLCHERQKDSCTKGFPAKDPVAEGHHYKKNPLGIPLNGCPLDERISEAHLLKREGNSVAALAMVTLDNPMCPGTGHRICNDCMKACIFQKQEPVNIPLAETATLTDVLNLPWGFEIYGLLTRWNPLNVRRPYALPYVGRNVLVVGLGPAGYTLSHYLLNEGFGVTGIDGLKIEPFPDALVGRNGHALQPIRDWSALTSELDERILEGFGGVSEYGITVRWDKNFLTLIHLTLARRESFRIHGGVRFGGTLTVEDAWALGFDHIAIAAGAGRPTIIGMKNNLIRGIRKASDFLMSLQLTGAFKKDSLANLQVQLPAIVIGGGLTGIDTATELMAYYPVQVEKALARHEKLVSQVGEEAVLARLDAEERATYQTFLEHGRAVREERQKAKALGRDPDFIKLVRAWGGVSLVYRRSLTESPAYRLNHEEVTKALEEGIRFIERMSPVEALPDASGAVRALRFERMVTVDGKLKGSGQVFELPARTVCVAAGTSPNVTYEKEYPGTFQLDARGEYFQSHELVDAEDGFSLVPVKAKEDPAAKTGFFTSYQQDGRFISFYGDNHPTYAGNVVKAMSSAKDGHPQVARLYAKEVAALDFTDEVAQAARDARRAAHFAKLDEAFTATVVAVNRLTPTIVEVVVRAPFAASHFSPGQFYRLQNFERNAPVVDGVRLTMEGLALTGAWVDKEKGLMGTIVLEMGSSSRLCAALKPGEPVVLMGPTGAPTEIGHNETVVLVGGGLGNAVLFSIARSLKAAGCRVVYFAGYRQKSDSFKHDEIEAGTDQIVWSVDTGDTIEPRRPQDSAFRGNVVQAMVAYAEGKLGPAPVVALADVDRIIAIGSDGMMRAVAEARHGVLQPHLKPGHEAIGSINSPMQCMMKEICAQCLQRHVDPVTGKETWVFSCYNQDQRLDQVDFVNLRQRLRGNTVMEKVADVYLAQLFKQAPHLKRV
>NZ_CP017169.1|WP_140796619.1|6761594_6762416_+|glycosyltransferase
MHAPFVSVVIPAYNEGQRLPRFVAELTRVFLERSAPPVEFVVVDDGSAPEQAELQRASVEAAQARLATAGARHQFTYVAAPRNQGKGLAIRLGWRHASAGVTWLAFLDADGAINAEEFHRLVAMSASEMAQNVDVLAGSRILMAGRRVVRSLHRHLQGRIFATLTDANFKLHFYDTQCGVKFVRADILRPLLDVLQEQRWLLDVELLVLLKRQGARFLEVPIDWEDFGGSKVIPGLDAARMFWGLLQLRRRLEHVSLPTHRDALPEGEPHAQR
>NZ_CP017169.1|WP_140856382.1|6760719_6761442_+|hypothetical-protein
MKLLGRDIPARELIARIEERLRTRGLPTSEEVELPPEGVEPRVEPLTFNLHALEEYADATRALPLHTHRGGVGQVVLLAKWAFRKSCQVFINEALGRQRVFNGHVRDSYAQLSAEVLRLRREVEALRSRPVPAVADAAVPQPSTASTTTTAPAIDAVLPKPRDTKAQSRQPVSAASTGKSAVPPPAAHAQAPVPAAGEPVTSKTARAKKAAPSAPAQPSAEASPRRNASGQKKRRNKKSR
>NZ_CP017169.1|WP_140856380.1|6758482_6760723_+|glycosyltransferase
MAIHQLIPSFVPGDATGQAALHLQLLLRRMGHAGALYADEVGPGLEGLASPASALRPAPGDLVLYHHGIASPLSSRLMHLPCRRGIVFHNISPARFYEGLPLADALVAGRAQLAAMAPFADVAIGVSDFNAAELRVAGYRNVHTVPLFIEPERFSRASADAKMLQRLEGPGPVLLGVSRVMPHKRFEDLLALHREVLRLRPQARLLMVGGYEPGSRYFRMLQREARGLRGVSFLGRLNHAQLVAAYRSASVFVSMSEHEGFGVPLIEAMAAEVPVLAYAAAAVPETLGGAGVAFDQKRFAFLAELAVDLSEDVSLRKPVIAGQTRRLEHFSAHSVQTGFTKALETVLPRPAPTKPRKAPERPRVALVVQRYGEVTGGAEKLAAQMAEHLAPHWDLTVLTTCAKNHLVWDNAFPPGPDVVDGIKVLRFPSTRVRNIRGFNGLSRQVFDKSNERLREEQWVAEQGPMCPGLLHHLATERDAYDGYLFFTYLYAPTVWGLPLVADRALLVPTTHDEAPVRFGVYRDVFERPRALLCLTPEEHTLIEKYFPNHAPTRVVGVGVDRPRADGARFKEKHGIHRHYLLYIGRQEPGKGVPELLQHHQALKERFEDAPDLVLAGDTNMELSGEGVRYLGRIDEQDKHDALAGALAVVVPSRYESLSLLTLESFAQGTPVLVNGRSDVLVGQVERSGAGRAYTDLESFIQGLREVGAERGPMGKRGLAYVKKQGWPQVVAAYREEMQRILEEKRR
>NZ_CP017169.1|WP_140858502.1|6757349_6758435_-|glycosyltransferase
MGPIAFDATLWDEPTTGIGLYTRCLASALEALGVQLTRVGARSSGEAPRAKAGRTAWTLGGLPRVLQGSDAPLYHAHGNFNLPLIRVPGMKYVLTVHDLIPLLMPETVSSAFRWQFRLWLSRSLMVADQVVCVSERTRQDLLARYPEAESRTVVVPNGVDHVHAPALDDTSKDFLRALSLPKEYVLYAGSLDVRKNVDLVLDALERLRLRGRPVSLVLAGQSWFGAGRVEARISRLRSEGFEVRSLGYQSDAVFYELMRRAAVFVFPSRYEGFGLPPLEAMRLGTPTIVSTAGSLPEVCGDAALSVGPDDANGLARALDRLLHSPEERRALAERGKAQAAKFTWKRTAEGTLAAYEAALRR
>NZ_CP017169.1|WP_140794438.1|6756786_6757341_-|hypothetical-protein
MRKLVWSGVMLCGLLAGCAGRQDTGTAPVEPPPAEAEASAEVSAPAPEDTQATEIPPAEEGEAKAAVQPLVVTPNPEPKDPINIRSAKVDGGILTVAVMHGGGCAEHTYSLAWDGNLQQGVDGTPVANLVLVHDGNNDRCKALLRASPRFDVSSVSQRFGAQFGKTSGTVNLVLSDQAQVRYDF
>NZ_CP017169.1|WP_140794437.1|6756261_6756783_+|DUF1768-domain-containing-protein
MSEAGQQRFTFFWQAHSPFSQWHRSDFVVDGVHYVCAEQYMMAGKARLFGDTEALASILSSKSPKTHKALGRKVRDFDNARWEKARERIVYEGNRAKFTQSEELLNALLATAGTELVEASPVDRIWGVGLDEEDPRIQHPAKWRGLNLLGKVLTKLREDLMAEGVTKASPAKP
>NZ_CP017169.1|WP_140794446.1|6769781_6770339_-|ribosome-recycling-factor
MSGDVVAELKGRIDKSIEGLRTDLTKVRTGRASIAILDGVRVDYYGTPTPLSGVASVNAPEPRLITIKPWEKSVLKDIEKALREANLGINPMNDGEMIRLPFPPLTEERRKDIAKQVKNKGEEFKVTIRNLRRDANEALKTQLKDKKITEDDHKRITEVVQKQTDAGITQVDEIVKKKEKEVMEV
>NZ_CP017169.1|WP_140794447.1|6770377_6771130_-|UMP-kinase
MSSDTKKPLPYKRILLKLSGEALMGEGKYGIHPPTLMGIAEEVIEVAQAGVEVALVIGGGNIFRGVAGATEGMDRASADYMGMLATCINSMAMQDALEKKGLHTRVLSAIKMEQIAEPYIRRRAVRHLEKGRVVIFAAGTGNPYFTTDTAASLRAMEINAQVILKATKVDGVYSADPKKDPTARRYRSLTYMDVLKQNLNVMDSTAISLCMDNKLPIIVFDLTQRGNIRRAVLGDGDIGTLVGGSETVWA
>NZ_CP017169.1|WP_140794448.1|6771346_6772000_-|translation-elongation-factor-Ts
MAEVSAQMVKELRERTNAGMMDCKKALSESGGDFAKAEEWLRKKGIAKAAGKEGRVASEGVIGTYVHSGRIGVIVEVNCETDFVARNPDFQELVKDVAMQIAAAGPKFVRREEVPTDNLDKEKDIQRELLKQQGKPEAMLEKILVGKMEKYYEGVCLVDQLWVKDDKKKVGEMISERAAKIGEKVSVRRFVRYEVGEGIEKKKDDLAAEVAKTLGQA
>NZ_CP017169.1|WP_140856389.1|6772158_6773136_-|30S-ribosomal-protein-S2
METQDTQTQQQAMAAAGGITMRQLLEAGVHFGHQTKRWNPKMKPFIFGARNGIYIIDLQKTVVMARSAFRFVADITARGGSVLFVGTKKQAQDVVREEAARAGQFFVTSRWLGGTLTNFKTIKQGIDRLKTLEKMAEDGTFERLPKKEVAQLEREREKLEKNLGGVKEMSKLPRCVFVIDPKKEHIAIHEAGRLGIPVIGLVDTNCDPDGIDFVIPGNDDAIRSIKLFTSKIAESCLEGAARYRASGAAERDEQEEREGRDDRGDRRDDRRGPRRGDRRDDRRDRGGDRGGDRRGPLVEMKAAAPVASTEPAAEAAALEGEAAAE
>NZ_CP017169.1|WP_140794450.1|6773515_6776338_-|preprotein-translocase-subunit-SecA
MIEWTLKKLIGTKNERELKKAHAKVARVNELETRMRALKDEDFVSETNRMRQEIQNGRSLDDLLFEAFAITREAARRVIGQRHYDVQLIGGMFLHEGCIAEMRTGEGKTLTATLPTYLNALSGRGVHVVTVNDYLARRDAEWMGRVYRFLGMTTGCVLHELNDKQRQEAYRSDITYGQNNEFGFDYLRDNMKFRLQDYVQRELNFAIVDEVDSILIDEARTPLIISGPTEDSTDKYYRVDQVIPGLVPDQDYTLDEKHRSVSLTDDGIEKLQKRLGVGNLYDPGEIEMLHHVDQALRAHTLYKRDKDYVVKDGEVVIVDEFTGRQMPGRRWSDGLHQAIEAKEGVKIENENQTLATVSFQNYFRMYSKLAGMTGTADTEAEEFAKIYNLDVRVIPTNRPPIRKDLQDVVYKTEREKFEAVAAEIEELHKAGQPVLVGTVSIAKSEVVASFLKKRGIPHNVLNAKQHQREADIVAQAGRKGAVTISTNMAGRGTDILLGGNAEVLAKASMGPPPEPPTSAPEGQPLDLTAYEAELAAWEQKLADTKTKLEEQTKKEREEVHNAGGLFIIGTERHESRRVDNQLRGRAGRQGDPGGSRFFLSLEDDLMRIFGSERIQGLMERLGMEEGEVIEHVWLSRAIEGAQKRVEGHNFDIRKNLLEYDDVMNQQRRTIYKLRRQVLAAGAGVPLVEYDEDPKTRIKTRSERTVSWADFRELILDSMEDVIVSLTDTYAPTRGVEGWDIAALQQGVKETFNLEMNFEGVGNREELQEHIYKAAEKVFQAREEEFGENFMRFLQYNYLATIDRLWKDHLLAMDHLRQGIGLRGYGQKDPKQEYKKEGYQGFIQMLSAIKAQFVTQLMHVQPRSASSAAEEAARIQRQLAQQQKKAVEGRATADGKLDEGSVAAAARPAAASKPAVGRNDPCPCGSGRKYKKCHGASEASV
>NZ_CP017169.1|WP_140799531.1|6776688_6777711_+|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM
MPARTLAARPGRWLWTCRAGFEAHLFEELEWAGAEPRLLGEALVESDAISGPPPAFARAGYQVAATLTATSPEAIAEAATRTVLALPGRAPWAVQAFTPDTPRGNALAPVAEALESAVSARLPPGRRVEDAQRAREAGALLVSLCVAPDDVTVVGAVHAREAVSLAAGGRRRMRRAGDAPSRAAMKLEEALDGLAFEPGRGDVCVDLGAAPGGWTQRLVSRGAKVVAVDPARLMPELTGNPRVKHVQESAFAYAPDEPADWLFCDMAWRPLEVAQLLAKWGRRGWAQHLVANIKLPMKDKNPILLRVRHTLVQEGGWEGLTVRQLYHDRDEVTVTAHKMK
>NZ_CP017169.1|WP_140856391.1|6777753_6778458_+|diguanylate-cyclase
MPYPLDDATATALIALHPWVLTRSPQAPVQAAVEVLVQAEQARRGQPDAKTGALQVPALTQGNLLKEEYDLSTHGHHDGWRVGAVIADVQGMINVNARFGFPTGDAVLRATVESLSAQYPGAKVVRIHADAFAALLVPTSQLTVEEHLAVPTRERLTQDVRRVLPQGTPDADVPSWTVSLLELTVDAPSHWQVLGPLLWAELERTHVMERTGRAQGLQRRRIRLDGSIPGPATL
>NZ_CP017169.1|WP_140794453.1|6778620_6779538_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MAKKSFTLMVIPDHDAPVKRYTIQRSFLTQVGMGLMLVVGLGVGASVHYFQVAADASENRILREENLTLRSQLKSVRERIEHIGSTLDRVERFDQKLRAVTLLSDPQRNLAMGPTEPEAGTSAPATDTQFTQLTSTETPKALMGRLDRLSAEATRQEQSLQELQAYFQDQKSLLASTPSIWPARGWVTSDFGSRLDPYTADRVMHGGMDIAAPHGKEVFAPSDGTVVFAGLEGGYGNVLVIDHGYGIKTRYGHLSKMLVKAGDRVKRGMHIAAVGNTGRSTGPHLHYEVRVNGIGQNPRKFILEE
>NZ_CP017169.1|WP_011555314.1|6779757_6780555_-|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase
MSSTAGQTAASRLKIISAGLTDVGRKRNHNEDSFLIDDELQLYVVADGMGGHAGGGTASRIAVETIDKEMRRAREGKDNPFLSVPNLQDSPIPEALRTAVERACLAIFTAAQEDARLSGMGTTVISLVVRDEHAFFAHVGDSRAYLIRGDLIQQISEDHSLVNEQIKAGMITPEEAKHSRYKNIITRSVGFEEEVQVDVMGLVSEPGDVFLLCSDGLANMMEDREIHETVVKARTFEEVPKRLIDFANERGGDDNITVIVVRVEA
>NZ_CP017169.1|WP_140856394.1|6780615_6782352_-|DNA-repair-protein-RecN
MLLGLRISNVAVIEEVEVAFGAGLTVLTGETGAGKSILVDALGLLLGGRADADVIRAGCEEASVEGVFARTPALESRLEELGLPDLGEEVLVRRVLGRTGRGKAYVNGSLVTVGVLGKLTRGAVDIAGQHEHVSLFDSGLHRVLLDRYGNLEEVLAAFFREYTGLREVDARMEALGGDEAKVRERAEFLRFQLDEITRLDPEAGEDARLDAERKRLGGAEKLKRHASEAELLVSGEEQSAVETVGRALGLVHESVKCDATLAPVAQALSTALSELEEAQRRLNRYVEGLESDPSRLADVEERLDALKRLCRKHGTHLDGLLKKQGEIEVELGTLENRKEILEELAADRRKVEERARKAATALTRARTASAVTFAAQVREGLGQLAMGKAAFEVRVTPSESLRPDGADDVEFFFSANPGEPPRALAKVASGGEASRLLLALKKALADSDGGGCYILDEADAGVSGAIADVVGRMIKDVSSHRQVLCITHLPQVAAYADAHLLIRKGLKGERTVSEVVVLEAGAERTRELARMMSGVEVTREALGAAEALVRSANRALGTRARRESGPEGSPRGRLRRTA

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Crispr_ID: NZ_CP017169_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_13

7818188-7818357

Orphan

Consensus_repeat	Method
CTCCACGGGGCCCATGCGCGTCTCCTCGG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP017169_13

>merge|NZ_CP017169|13|7818188-7818357|CRISPRCasFinder
CTCCACGGGGCCCATGCGCGTCTCCTCGGTGAGCGGCTCCACCGGGCCCATGCGCGTTTCCTCGAAGCGAGGCTCCACGGGCCCCATGCGCGTCTCCTCGGGGCGCGTGAGGAGCGGAATGTCCCGCGTCGCGTCCTCGTCCTCGTCCGGGGCGATGCGTGGCTCCTCGG

>NZ_CP017169|13|12|7818188-7818357|CRISPRCasFinder
CTCCACGGGGCCCATGCGCGTCTCCTCGG	TGAGCGGCTCCACCGGGCCCATGCGCGTTTCCTCGAAGCGAGG
CTCCACGGGCCCCATGCGCGTCTCCTCGG	GGCGCGTGAGGAGCGGAATGTCCCGCGTCGCGTCCTCGTC
CTCGTCCGGGGCGATGCGTGGCTCCTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_174258950.1\|7822953_7824630_+\|bacillithiol-biosynthesis-cysteine-adding-enzyme-BshC	unknown	unknown	gnl\|CDD\|274913
NZ_CP017169.1\|WP_140799899.1\|7809438_7810947_-\|tail-fiber-domain-containing-protein	unknown	unknown	gnl\|CDD\|240612
NZ_CP017169.1\|WP_140795173.1\|7818490_7820203_-\|sodium:solute-symporter	unknown	unknown	gnl\|CDD\|271385
NZ_CP017169.1\|WP_140857055.1\|7820375_7822859_-\|PIG-L-family-deacetylase	unknown	unknown	gnl\|CDD\|376836
NZ_CP017169.1\|WP_140857059.1\|7824626_7825433_+\|bacillithiol-biosynthesis-deacetylase-BshB1	unknown	unknown	gnl\|CDD\|274915
NZ_CP017169.1\|WP_140795168.1\|7810989_7812609_+\|DUF4041-domain-containing-protein	unknown	unknown	gnl\|CDD\|214947
NZ_CP017169.1\|WP_140799898.1\|7805685_7807656_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017169.1\|WP_140857045.1\|7803373_7804765_+\|ammonium-transporter	unknown	unknown	gnl\|CDD\|223083
NZ_CP017169.1\|WP_140857049.1\|7815156_7817307_+\|catalase	unknown	unknown	gnl\|CDD\|236886
NZ_CP017169.1\|WP_140795163.1\|7804839_7805523_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP017169.1\|WP_140857047.1\|7814349_7815000_+\|SRPBCC-family-protein	unknown	unknown	gnl\|CDD\|176860
NZ_CP017169.1\|WP_140857063.1\|7829237_7830173_+\|proline-racemase-family-protein	unknown	unknown	gnl\|CDD\|172473
NZ_CP017169.1\|WP_140795169.1\|7812810_7814226_+\|L-serine-ammonia-lyase	unknown	unknown	gnl\|CDD\|273233
NZ_CP017169.1\|WP_140857053.1\|7820199_7820379_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140857065.1\|7830169_7831306_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223737
NZ_CP017169.1\|WP_140795166.1\|7808535_7809360_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140795165.1\|7807570_7808521_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_174258951.1\|7827689_7828982_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|379114
NZ_CP017169.1\|WP_140857061.1\|7825429_7826593_+\|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA	unknown	unknown	gnl\|CDD\|274914
NZ_CP017169.1\|WP_140795179.1\|7826613_7827471_-\|DUF2911-domain-containing-protein	unknown	unknown	gnl\|CDD\|378565

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_174258950.1\|7822953_7824630_+\|bacillithiol-biosynthesis-cysteine-adding-enzyme-BshC	gnl\|CDD\|274913	TIGR03998, thiol_BshC, bacillithiol biosynthesis cysteine-adding enzyme BshC. Members of this protein family are BshC, an enzyme required for bacillithiol biosynthesis and described as a cysteine-adding enzyme. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	0
NZ_CP017169.1\|WP_140799899.1\|7809438_7810947_-\|tail-fiber-domain-containing-protein	gnl\|CDD\|240612	cd12820, LbR_YadA-like, YadA-like, left-handed beta-roll. This group contains the collagen-binding domain virulence factor YadA an adhesion proteins of several Yersinia species, and related cell surface proteins, including Moraxella catarrhalis UspA-like proteins. The collagen-binding portion is found in the hydrophobic N-terminal region. YadA forms a matrix on the bacterial outer membrane, which mediates binding to collagen and epithelial cells. YadA inhibits the complement-activating pathway with the coating of the cell surface with factor H, which impedes C3b molecules. These domains form a left handed beta roll made up of a series of short repeated elements. UspA1 and UspA2 are part of a class of pathogenicity factors that act as cell surface adhesion molecules, in which N-terminal head and neck domains extend from the bacterial outer membrane. The UspA1 head domain of Moraxella catarrhalis, is formed from trimeric left-handed parallel beta-helices of 14-16 amino acid repeats. The UspA1 head domain connects to a neck region of large extended, charged loops that maybe be ligand binding, which is in turn connected to an extended coiled coil domain that tethers the head and neck region to the cell surface via a transmembrane region.	1.33464e-20
NZ_CP017169.1\|WP_140795173.1\|7818490_7820203_-\|sodium:solute-symporter	gnl\|CDD\|271385	cd11494, SLC5sbd_NIS-like_u2, uncharacterized subgroup of the Na(+)/iodide (NIS) cotransporter subfamily; putative solute-binding domain. Proteins belonging to the same subfamily as this uncharacterized subgroup include i) NIS, which transports I-, and other anions including ClO4-, SCN-, and Br-, ii) SMVT, which transports biotin, pantothenic acid and lipoate, and iii) the Na(+)/monocarboxylate cotransporters, SMCT1 and 2. SMCT1 is a high-affinity transporter while SMCT2 is a low-affinity transporter. This subgroup belongs to the solute carrier 5 (SLC5) transporter family.	6.79694e-147
NZ_CP017169.1\|WP_140857059.1\|7824626_7825433_+\|bacillithiol-biosynthesis-deacetylase-BshB1	gnl\|CDD\|274915	TIGR04001, thiol_BshB1, bacillithiol biosynthesis deacetylase BshB1. Members of this protein family are BshB1 (YpjG), an enzyme of bacillithiol biosynthesis; either BshB1 or BshB2 (YojG) must be present, and often both are present. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	1.91777e-114
NZ_CP017169.1\|WP_140795168.1\|7810989_7812609_+\|DUF4041-domain-containing-protein	gnl\|CDD\|214947	smart00974, T5orf172, This entry represents the putative helicase A859L.	1.04596e-18
NZ_CP017169.1\|WP_140799898.1\|7805685_7807656_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	5.85603e-103
NZ_CP017169.1\|WP_140857045.1\|7803373_7804765_+\|ammonium-transporter	gnl\|CDD\|223083	COG0004, AmtB, Ammonia permease [Inorganic ion transport and metabolism].	4.08701e-156
NZ_CP017169.1\|WP_140857049.1\|7815156_7817307_+\|catalase	gnl\|CDD\|236886	PRK11249, katE, hydroperoxidase II; Provisional.	0
NZ_CP017169.1\|WP_140795163.1\|7804839_7805523_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	5.79629e-13
NZ_CP017169.1\|WP_140857047.1\|7814349_7815000_+\|SRPBCC-family-protein	gnl\|CDD\|176860	cd07818, SRPBCC_1, Ligand-binding SRPBCC domain of an uncharacterized subfamily of proteins. Uncharacterized group of the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands. SRPBCC domains include the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), Class I and II phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of the superfamily include PYR/PYL/RCAR plant proteins, the aromatase/cyclase (ARO/CYC) domains of proteins such as Streptomyces glaucescens tetracenomycin, and the SRPBCC domains of Streptococcus mutans Smu.440 and related proteins.	2.53339e-68
NZ_CP017169.1\|WP_140857063.1\|7829237_7830173_+\|proline-racemase-family-protein	gnl\|CDD\|172473	PRK13970, PRK13970, 4-hydroxyproline epimerase.	1.05715e-133
NZ_CP017169.1\|WP_140795169.1\|7812810_7814226_+\|L-serine-ammonia-lyase	gnl\|CDD\|273233	TIGR00720, hypothetical_protein_NEICINOT_00681, L-serine dehydratase, iron-sulfur-dependent, single chain form. This enzyme is also called serine deaminase and L-serine dehydratase 1. L-serine ammonia-lyase converts serine into pyruvate in the gluconeogenesis pathway from serine. This enzyme is comprised of a single chain in Escherichia coli, Mycobacterium tuberculosis, and several other species, but has separate alpha and beta chains in Bacillus subtilis and related species. The beta and alpha chains are homologous to the N-terminal and C-terminal regions, respectively, but are rather deeply branched in a UPGMA tree. This enzyme requires iron and dithiothreitol for activation in vitro, and is a predicted 4Fe-4S protein. Escherichia coli Pseudomonas aeruginosa have two copies of this protein. [Energy metabolism, Amino acids and amines, Energy metabolism, Glycolysis/gluconeogenesis].	0
NZ_CP017169.1\|WP_140857065.1\|7830169_7831306_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|223737	COG0665, DadA, Glycine/D-amino acid oxidases (deaminating) [Amino acid transport and metabolism].	1.04187e-50
NZ_CP017169.1\|WP_140857055.1\|7820375_7822859_-\|PIG-L-family-deacetylase	gnl\|CDD\|376836	pfam02585, PIG-L, GlcNAc-PI de-N-acetylase. Members of this family are related to PIG-L an N-acetylglucosaminylphosphatidylinositol de-N-acetylase (EC:3.5.1.89) that catalyzes the second step in GPI biosynthesis.	5.25425e-21
NZ_CP017169.1\|WP_174258951.1\|7827689_7828982_+\|AAA-family-ATPase	gnl\|CDD\|379114	pfam13304, AAA_21, AAA domain, putative AbiEii toxin, Type IV TA system. Several members are annotated as being of the abortive phage resistance system, in which case the family would be acting as the toxin for a type IV toxin-antitoxin resistance system.	6.67343e-07
NZ_CP017169.1\|WP_140857061.1\|7825429_7826593_+\|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA	gnl\|CDD\|274914	TIGR03999, thiol_BshA, N-acetyl-alpha-D-glucosaminyl L-malate synthase BshA. Members of this protein family are BshA, a glycosyltransferase required for bacillithiol biosynthesis. This enzyme combines UDP-GlcNAc and L-malate to form N-acetyl-alpha-D-glucosaminyl L-malate synthase. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	0
NZ_CP017169.1\|WP_140795179.1\|7826613_7827471_-\|DUF2911-domain-containing-protein	gnl\|CDD\|378565	pfam11138, DUF2911, Protein of unknown function (DUF2911). This bacterial family of proteins has no known function.	1.65602e-63

>NZ_CP017169.1|WP_140857049.1|7815156_7817307_+|catalase
MKPRKPSAKTRPTTLKSESLEPHRMHTEGKVLTTDQGIPISDTDNSLKAGIRGPTLLEDFHFREKMMRFDHERIPERAVHARGAGAHGYFQVYKSLEKYTQARFLTDPSLRTPVFVRFSTVGGSRGSADTVRDVRGFATKFYTEEGTFDLVGNNMPVFFIQDGIKFPDFVHAVKPEPHNEIPQASSAHDSLWDFVSLVPETTHMIMWLMSDRAIPRSFRMMEGFGVHTFRLVNAAGKATLVKFHWKPLLGNHALAWDEAQKLSGKDPDFHRRDLWESIEKGDFAEYELGLQFIPEGDELKYGFDLLDATKLLPEELVPVQRVGKLTLNRNPDNFFAETEQVAFCVANVVPGIDFTNDPLMQARLFSYLDTQLTRLGGPNFAELPINKPVCPVTNHQQDGFGRQTIPTSRANYHPNSLGGGCPVLANPTNAFRHYQERVEGHKIRARSGSFSDHFSQATLFYKSLSKPEQEHLVAALEFEIGKVKRVEIRERVVNQILVNVDPELAVRVARAVGVTPPKVSKPPKPSKAAGKKAAPSVETSPALSMENSPHDSIRTRKIAALVSDGFAGKELDGVRKVLEERGATLELVGPTLSPVTSQEGREERPLRTFSTASSVMYDAVYVPGGEKSVAALRRVPLAVDFVREAYVHCKALALSADADTLLDAAGVRDLEAPPSKGLDATRGVVRSAKMETKGFGQLFAESIARRHWEREAPPPA
>NZ_CP017169.1|WP_140857047.1|7814349_7815000_+|SRPBCC-family-protein
MLKKILVGLAAVILLFVGFVVTRPDTFTYQRAAVLPVSADIAFALVNDFHRWTEWSPWDGLDPQAQRTYSGAESGTGAGYAWVGNDQVGEGRMTITDSKANEQVTIKLEFIKPFAATNTSTFAFSAAEGGTQVVWAMSGENNFVSKAMSLFMDMDAMIGKDFEKGLATMKDVAVANAKKHAEAEAARIAEEKARTEAAAAAPAGEGAPAVAAPAVP
>NZ_CP017169.1|WP_140795169.1|7812810_7814226_+|L-serine-ammonia-lyase
MAVSVFDLFKIGIGPSSSHTVGPMRAARMFARKLADTGVLERLTRLKVELFGSLGATGKGHGSDKALVLGLMGETPEGVDVEAVPAIISRWRAEGRVALLGQREVTFRDGEHLVMHRRRSLPFHPNGMRFTACGGDGAELASAVYYSVGGGFIVDESAAVAGKDPLSKDTTPLPFPFQSAAALLAHCERERMSFSSLMLANEKTWRDEAEIRAGLLRIWDVMQACVRRGCTSGGILPGGLKVERRAAGMYQKLISRPEAGLTNPLTVLDWVNLYALAVNEENAAGGRVVTAPTNGAAGIIPAVLHYYWRFVPGANEDGVVRFLLTAGAIGVLYKENASISGAEVGCQGEVGSACSMAAGALTEVMGGTPLQVENAAEIAMEHNLGLTCDPIGGLVQVPCIERNAMASVKAINATRMALSGDGRHFVSLDKVIRTMRDTGRDMKDKYKETSRGGLAANVLEVANLSVGLPEC
>NZ_CP017169.1|WP_140795168.1|7810989_7812609_+|DUF4041-domain-containing-protein
MQPAVWVLGLVSLLSSGLLVFTAIRLAAVKRRFKPVLDVEAERQRVLSELTREKAESTHTLAMERNRVAAELTRERSDTAQSLAAERNRVTAELTRAREDAEAAIQSARLNLVHAKEENERAISQAQTQAQAEATRIREQAEKDAREAEVQRQQAQVERTQLENTISRLAAELRPLEEESVLRSYGLYKPVYNFSTSEKYEERLEDIRERQKEMLKEKKAAFCKIEWEVNGSKAEGRKQTERTLKLMLRAFNGEADACVAKVSYKNVKAMEARIQKAADAISALTEIQQCFIATKYVDLKLDELRLAHEYQEKLQQEKDEQRRIREQMREEEAAQRELERARLEAEREARRDEEALRKARTEFEQSTGAQQQRLQERIAELERRLAEDLERQRAISQAQLTRTGHVYVISNIGSFGEDVYKVGMTRRLVPMDRIDELGDASVPFEFDVHAIIRTHDAPKLESELHRTFANRRVNRINERKEFFRVSLDEIAEAVREHHGDFELTRVAEAAEYRKSLALIDEERNGAETSTASAPRRAVA
>NZ_CP017169.1|WP_140799899.1|7809438_7810947_-|tail-fiber-domain-containing-protein
MAASTAHGGGRCSVNARASRNPPSGVWTFPRRKSVGVVSYPDSTPGDEMRGRELFAAMSCITLATTGCGSEGPPAQNWEVGSGLRLDDSNVVSVAYGTGPGTVVEGSDPRLSDARPPLPGSGGYIQNGTQPQDASLSLAGTASTRSGLFVDAAAAVSSPVPLLRVTNTSEAQPVWDALPVFTVDSGGGLLARGAYELGAPLPMSGRGMRLMWAPARGVFRAGNAETEWDIANVGEYSWAGGNRSRASGYGTFAFGDQCVASGTVAVCFGSSNQATGTASFTSGASNTASGFGSTALGYTSTAAGQGSVALGYSAQATGDYGVALGYRVSTGGRTGAFIWGDGSTTTATSTADNQFMVRAAGGVRLRTRADLGTGCDLPANSGVFTCTSDRNMKEDFRHVDGEALLAKVAKLPVESWRYKGEDRQVRHLGPVAQDFRAAFGLGTDDTSIGMLDIDGVNMAAIQALERRTRELNAKSAELDALKAELAELKASVAQLKASLPRP
>NZ_CP017169.1|WP_140795166.1|7808535_7809360_+|hypothetical-protein
MRFQRFAFAAMSFACTAAMAAEPIQPPWGKESNLGEKMMLEATSVCTDGKGHFVALTPDDEDTNAVLYYGDEKQFVQVPRPGPYTSATSFLDPRFFNKGANPNFRGIDWRVMSSVEIDRKERTCSLTCGEKKIPLTMLDGEPASELLRKASFQPNPQKFVPYALLRDTKGAYYFVDRGFHEAEKKSYRVFIGPRGSLKAQKMTNVISDSEGEIFSTKRGDLRLLLDKAKPALWIENTKRRLELRQVPVDENLPLIYNELGVYEGARLGTPCDDQ
>NZ_CP017169.1|WP_140795165.1|7807570_7808521_+|hypothetical-protein
MRSASGPRSRQRSVPRSRSSARSTTSSSETAGHPGRGALMQHEVIRLRNMVAVIVAAVALGASQALAAAPVEAGKVYSGTEGEEVAVVPLTPRSDKKFILRVKGTGSEFDGLVFPYEQNDWSTRSTEQFNYSTQWHGRKYTALHVRDTKYELYVPGRQRPIRLAYDEKKTAALKPEEVYAQHQKQMKDGSLAKLMAFDRKGEESGHEKEFAATLQEMNNACGTSVAARIDWSSINEDQLKELSISSFCGTPLTSLKELCTASAIAKQTIQEKVKQVSCRFGSALEPKIEADRVIWTTSRDASNQDKFATKYFKQNL
>NZ_CP017169.1|WP_140799898.1|7805685_7807656_+|protein-kinase
MTLPADGDLRIDEVLRNTYRIVSLLGRGGMGSVYLAQHLRLPGKQVAVKVLRGGDHLTPEIFARFRREAEIASRLGHPNIVEVLDYDTLENGNPFLVLEYLRGESLQERLERGRLPMEDVVSFTRQMGSALQAAHGAGVIHRDLKPANVFLVPTDSGGVVGERVKLLDFGISKVLSSTTVQTQEATIIGTPQYMSPEQAQGKNRDIDARTDVFALGCIVYEMMAGKPVFGSGSLAQMIFRVVYEPPEPLAPLCPEATPEAISAVMRALAKSVDERYPDVSTFIADLTGTPLHSLSTTAGNQPAPRPQAPTSGIALPSAGPSSLSATVPPGSLKVAPDTGREGFDSTMAPGTGQQGFSPSATGQMGVAQAQGFSPSATGQMGVAQLSAASLIDPPGLEPTLISKQLPAIPVQERPAQHHTAVSVPVPIPSAAEAHAAAALLSAPSTPVSSPPAAKGRGAIIGATAAVLLASSMGLVWWMKGGTSGSGSPTTPVTDTRVPQDAQQANGTQQANGTQQANGTQQANGTQQANGTEQANGTQTPPDTDNPQQVVVATNTVPDKPTSRPVTRPEAKEELPEQVRKLLKDGESALASGDASRAIALARSSQRTKRSMAAYSLLTRAYCQQKDLGGAVSEWPKVASAERAKVKKFCQKHDIEL
>NZ_CP017169.1|WP_140795163.1|7804839_7805523_-|GNAT-family-N-acetyltransferase
MPKAKTPKPPDSLEVRVRRIHRRDLNRTWEFLKLVFRDVNRETVEYQRPRSKRRFLEVYTSEWIEQLLYEVDGSIVGYSECAFEATGDDNWVNPRWFEKRGMRPLFVEELAVHPDYQGRGVGSFMLDQLQHLARTRGCTHLVLEVAENNESALTWYRTRSFYKLDAAIFMAQKVPGEPDLLPPRRLKRRQKPTAEAGTPSTGPMPETAPTRAATRKARAPAARKKSS
>NZ_CP017169.1|WP_140857045.1|7803373_7804765_+|ammonium-transporter
MKKWFAMALLVGVGVVGLLVEPAAQLKQGGPINTADTAWILTATALVLLMTPGLSFFYGGMVRLKNVVSTLLQSFIAMAVISLIWVVVGFSLCFGDSFHGLIGDPRTFFMFSGVGGETHPDLAPTIPLMLFALFQLKFAIITPALITGAFAERVRFKAYVLFMVLFTLVIYAPLAHWTWHPEGFLRQWGVLDFAGGTVVHMSAGFAALAGALVLGRRKVHVENTTHAPANIPFVMLGTGMLWFGWFGFNAGSAMSASSLATLAFATTNTASAAAMLGWIAFDWLRGRKPSAMGACIGAVVGLVAVTPAAGFITVGQSIVVGLVASFVSNAAVHFKNRTSVDDTLDVFPCHGLGGVVGMVLTGVLAKDVGLIHGETRTFMMHMLALVLVSVFSFAGSFLLYKLVDRIVPLRVTREHEEEGLDLSQHGETVGESIIAPGPQSALTATTAVATEPASDASSLPQPA
>NZ_CP017169.1|WP_140795173.1|7818490_7820203_-|sodium:solute-symporter
MTGLDWVVLGGTIAFIVVWGIWKSRGAASSEEYLRGGRELKWPTIGLAVMATQASAITFLSVPGQAYEDGMRFVQFYFGLPIAMIIISAVFVPIYYRLNVITAYEYLESRFDLKTRLLGAFLFLIQRGLAAGITIYAPAIILSAILGWPLEPTVIVMGAVVILYTVTGGAKAVSQTQKQQMVVMMGGMVVAAIVIVWRLPEHVSFGKAVDVAGAFGRMNVVSFDFDMQDRYNFWSGITGGLFLSLSYFGTDQSQVGRYLSGRSISESRLGLLFNGVLKIPMQFLILFVGILVFAFYQFSTPPLLFNEALRTRVQGTAQAAEYAALESKWEQVQSGKRAEVERYLSAVDSGDVAAGDASRALLQGHAQEASAVRKEAKDLVVRALPGAETKDSDYIFISFVKRWLPSGLFGLLIAVILSAAMSSIASELTALGTTTTVDFYRRVFQRNASDRHVLVASKLFTVFWGVVAVGFATFASLLDNLIQAVNILGSIFYGTVLGIFLVAFFVKHVRGHAVFAAAVISQATVIALFFLSDVGYLWFNVIGCALVVVLGLVMQAVLPRGETPAPATGA
>NZ_CP017169.1|WP_140857053.1|7820199_7820379_-|hypothetical-protein
MSTAPHLNPSEPSAEAPAPRPELDDAPPLLGSWRNIYILVLGTFALFLALGWVLTEVYS
>NZ_CP017169.1|WP_140857055.1|7820375_7822859_-|PIG-L-family-deacetylase
MRNLLLGMTLAMSLGIGSTAVAQPPRQLHAGEIAAGLKRLGVTGSVLYVAAHPDDENTRLLAWLVGDRGLRAGYLSVTRGDGGQNLIGTEQDALLGLIRTHELLAARSVDGAEQFFTRARDFGYSKSAEEALRIWGHEAVLADVVLAIRRFQPDVIITRFTTEPPNHGHHTASALLAAEAFIAAADPKRFPEQLSEVKPWKTDRLLQNASQWWFKPDEDLSRYVKLEVGGYDALLGRSWGEVAAESRSQHKSQGFGQATDRGPSTEYFTPLAGTLPKRDVFEGLDFSWKRWKGAEAVSRAVAAATKAFDARAPHRSLPALVRVHEALTALPDTHPWKAPKLRETEALIAACAGLFLEVRASAPTGIPGLPVALDVVALNRSPAAVEWVGLTLPGEKPEAVGKALGANVPLKLSRTVTLPTTAPISTPYWLREPVTGGLYTLEGEDRALTGQPEGVPALSVAFEYKVAGRRFRAVRPVVYVWTDPVSGELYRDFEVVPPVTATLAQDVLMFPNGESRVVPVVLAAGMDQVPGTVRMVAPPGWRVEPASVEFKLATRGDERTITFQVTPPQGSTQKGDLSVDVDVGDRAWSWRARSVSYPHIPPLTVRQPSTATVVPFSLAMKGKRIGYIPGPGDRVAESLSAVGYEVTLLPEERLAREKLERFDAILVGVRAFNANTHLTVHRERLLQYVEGGGRLVVQYNTNSRVGPLTSFVGPYPLEIGRDRVTDETAVMTPLRADEPLLRTPNALTAADFEGWVQERGLYFASSWDARYQPVFAMHDAGEAPLQGALLVARHGKGTFVYTGLAFFRQLPAGVPGAYRLLANILSQ
>NZ_CP017169.1|WP_174258950.1|7822953_7824630_+|bacillithiol-biosynthesis-cysteine-adding-enzyme-BshC
MHFRWRVRRDLLSRHAVTSSFSTAWLRGDASALSFLSDDYRHREARARAVAAAAASRRVSPALLDVLGAQNARLAPSPARERNLALLAQPGTVAVVTGQQMGLFLGPLYTLYKAASAIVTARALREETSRPCVPVFWLQTEDHDLPEIDHCVIPRPGGGPCRLALELPDAAASRAPIAHRHLGPSVLPALATLRAELEAEPHAEEFLSLLERAYRPEATLAGAFTDVLASLFADEGLVFVDPRDARLAPLAAPVHRFALQEAGALASVLAARTEALTRAGYTVQVHVRPGSPLSFFSPDALDGPRYRLDPAEAGAWSLVGHPDSSAITQDALHAALEREPLRFTTSALLRPLLQDTWLPTAAYVGGPGELAYFAQLAPLYAHAGRPMPLAIPRARFRVLDDRARRWLGRVGLQPDEVNVPRDTLLTRLATRDAPESLETPEALEARLFGAFSSELERVAGQVSAVDANLQDALRRTEGTVRVAVSRLTGRYRRALARRDATAAEQVDRLRTFLFPEGAPQERVLGLPYFACRIGARAFTQLVLDACVPFSGDSKDLTP
>NZ_CP017169.1|WP_140857059.1|7824626_7825433_+|bacillithiol-biosynthesis-deacetylase-BshB1
MSANGTAYGIDVLAFGPHPDDVELFCGGLLASMAAHGYRTGIVDLTRGEKSSRGTLQSRAEETEAATRALGLAHRENLELPDGWLNPWAGFDTPEPERARTAAVARVVEALRRLRPELVVVPWEQERHPDHEAASALVTRALFFAGVRKFDAEPAAEPFTPRQVLYYPLRHLAEPSVVVDVSAVYERKLAAVHCYASQVMPRPDAPPTLVGSPLSLSSLEARDRFYGAQIGVTHGEPYVLREALGLADPLDHFRRNSFARPLFFPART
>NZ_CP017169.1|WP_140857061.1|7825429_7826593_+|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA
MNAPLNVAITCFPTFGGSGMVATEIGLAMADRGHRVHFIARDLPVRLHGANRKVVFHEVTESDYPALQQSSTYPIALASKMIEVANYERLDILHVHYAVPHATAAWMAREVLGHKAPRVVTTLHGTDTTLVGIDPSYLPITRFSITRSDAVTVPSAYLRRATWRGFDIPESVPIDVITNFVDTTRYAPVRDRACLRALFPALRDHEPVLIHVSNFRPVKRIVDVVAIFTEVHRHRPCRLVMVGDGPERSPAERMLREMGLEGRVAFLGKQDRFEELVAASDVFLLPSEQESFGLAALEALSCGIPVVASDLGGIPELVTHGETGFLAPLGDVPAMARHVLTLVEDAERWQGFSHRARAQVLERFQKEPAIDRYEALYRRLLTGPLRR
>NZ_CP017169.1|WP_140795179.1|7826613_7827471_-|DUF2911-domain-containing-protein
MRTMKNQLLSCMASALMTLSAMPALAQLKLPAASPAAKVTQEVGVSEISVEYSSPAVKGRKVWGELVPNDKAWRSGANSATKITFSHPVTFGGKAVPAGSYAIVSLPSQKGWKVMLNTDLGLWRGGAPYDTAKDVASVSATTTEIPSRERLTYLFTDTTDTGTRLDLEWEKLRISVPITVDTAALAKANIEQAQKSTAMMHASAASYVAEATKDYAAALNHADAAVAANPTWYNHWVRAGVLSQMGKYSEARKAAQAAWDLGQKDKNFFYRDQVSKALAEWKNKK
>NZ_CP017169.1|WP_174258951.1|7827689_7828982_+|AAA-family-ATPase
MKLTRLEVHHYRNVVPGTSLVFSPSCNLVLGENGTGRTTLLELISTVLGSDFSGLIHEPFALEYDLAFPGMKLHVFVRNEENAPAPDAEAPPRKGSALMPLRTPALDSSLHPRIEVDVQFHSPSARLVMRADAAGMDCKVDGEAVWSRSMHWSLLDRSVWTLLFMTAQYIDAGMKERLKELLRRTFLLAPQRFDEALGMFERIGAIRYAMEVRDGEVFPLGLMALPTWMPGWLREQMEQPSVTDVLELTHDAREGSFLAKFVALAGFEAGRFRVEVLEKRSFENGGRVGFGGFGFEFTRRDGRVLTHEALGFGQKRLLSLLYYLDVNEDFAIADELGNGLHPRWVEASMREMGARQVFLTSQNPLLFEHTLFPSAEALRASLLLCGNTREDGPERIAWKNPTHEVAGRLFDAHGLGAHPLAELLRQQGLW
>NZ_CP017169.1|WP_140857063.1|7829237_7830173_+|proline-racemase-family-protein
MRRIRVIDSHTGGEPTRVVTDGGPELGAGDLASLRERFREKFDAFRKAIVCEPRGSDVMVGALLCPPVSASSVAGIIFFNNVGYLGMCGHGTIGVVKTLEYLGRIGPGVHSLETPVGVVKATLHPDGRVSIANVPSYRWAHDVAVSVPGHGEVRGDIAWGGNWFFLSRATHLPLELSRTPALLAYTSAIKQALSDQGITGEGGAEIDHVELYAPSPTPGVDARNFVLCPGLAYDRSPCGTGTSAKVACLAAEGVLAEGATWVQESILGSRFEARYVRDGARILPTITGTASVNAEATLLVEPTDPFAWGIG
>NZ_CP017169.1|WP_140857065.1|7830169_7831306_+|FAD-dependent-oxidoreductase
MSAFDCVIVGGGIVGAALADVLSADGVSVALVEARSIGAGTTACGMGHLVAMDDNAAELALTSWSVSLWRELADGLPRAVEYDACGTLWLAADDEEMAAVSAKVANYRAAGVRAEVLDSAALHEAEPALAPGLVGALRVVDDAVLYPPLAARTFALRARARGARLMTGCPARELRSGSVVLSNGEVLTARHIVLAAGVASPTLCPGLPISPRKGHLLITRRGAPVVHHQLVELGYLKSAHGTDSASVAFNAQPRVTGQLLLGSSRQPGDATREVDAALLERMLKRAAMFLPGLDGLQALRVWTGLRPATPDGLPLLGPHPEKPWLWLACGHEGLGITTATGSARLVADQLLGRTSPIDARPYSPARFLAVSSREVAHA

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Crispr_ID: NZ_CP017169_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017169_14

8784954-8793564

TypeI

Consensus_repeat	Method
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	PILER-CR
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CRISPRCasFinder
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CRT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	PILER-CR

121 spacers

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

The CRISPR arrays of NZ_CP017169_14

>merge|NZ_CP017169|14|8784954-8793564|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGACGAGCAGGGGTAGGCCGGCGTCCGCCTTGAAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACTATCTGCTGCGGCTGCGGCGGCCTCTGCGACTGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGTTCCACCAGGCGGCAACCTTCACCGTGGTCCGGTTTCAACCCACGCTCCTCGCGCTCACGAGGAGCGACGAGTTCGAGGCACTGCACGACACCTTGCTGCGCAGTTTCAACCCACGCTCCTCACGTTCACGAGGAGCGAGCCCATCTTGTAGCGCTTCTCCGTGGGCCGCTTGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGTGGCCTGCGGCCACGGATGACCGGATACGCAGCAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACTTACGCGGTGGAGCAGGATTTCGCCCCGGCGCTGGCGTTTCAACCCACGCTCCTCGTGTTCACGAGGAGCGACGGTGCCTGGCCCCGCTGGCGTTGAGCCTGTCGAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACTCGCCGCGCCTGGGTGTCGTTCCGCCCCTGGTAGTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGACTGCAGCACTGAGCATGCCGCGCAATCACGACCCCCGGTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGAATCGCCCGCGTGGTGAGGATTGACGGCGTACCCGTCGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACACTACGCCCGCGTGTTGGACTTGCTCTGCGAGGGGGTTTCAATCCACGCGCCTCGCGTTCACGAGGAGCGACACCGCGTACCTGGACTGGGTGGAGGAGCAGGCCGAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACCTCCAGGCGGCGCGCCGCGCAACGTTGCGGCTGGTGTTTCAACCCACGCTCCTCCCGTTCACGAGGAGCGACTTGCCCTGCGTCTTCTTCTCGATGCCGCGCCAGTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTTTTCGAGGGCACGCCGGTTGAGCGGCGCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCTCGACCGGGGCGTCAGCCTCTGCCGCAGCCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTGGGCTGACGTCCAGTCCTGCCTGCTGGCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGCTTCCCCGCAGTCCCAGGAGCACCCCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCTGGCGACCTGCGGCGGCAGAGGGCGGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGCACCCCATGGCCCTCGCCACCGACATGCTGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAAACGCCGGCGGAGGCGCGGCCCCAGGTACATCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGATGGCTTCCCGTGCGCCGGCCAGCGCAATGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCACGTCCGCCGACCGCGAGCGCGCGATGACGTATCTGTTTCAACCCACGATCCCCGCGTTCACGAGGAGCGACAGCTCGCCCACGGACACGCCGGCGGAGCTGGCGCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCTCTGCTGCGGGTGAGTCGCCAGCGCCGGAGTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCAGATGCTGTCTGACGTGTTCGTTGTGGCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGGACGCTTGGGCGGGTCCTGGGGGGCGCCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCTGGAGTGGTAGACACACCCCTTGCAGCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGGCACCTGCTGCGCGAGCGGCGCCACCCCTTGCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCCAGGCTTGGGGGTTGCCGGACGGGTGAAGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGGCAAGTGCCCCGCGGCCCATTCGACAACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCCCAGCAGCCTCGCGCCGTTCATGTTCGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCCCCGGGCATTGTTCGCATCGAGGTGAAGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCCACAGTCCGACTAGCGGGCCGCCTGCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCCCCGGCGCTGGCCGTCCGAAGGGCAGCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGACGACGTAACGGCCATAGCGCAGGTGAAGGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCATCACCGAGCAGCGTCAACTGGTTGCGCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGTCATCGCAGACTGGGGTCAACCTCGTAGAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCAAGCTCTGTCGAGCCTGCTTGGTCGGCCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGGCTGTCTTCTCGTCACCGCACGTCGCATCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGGCCATGGCCGCGTTGCGCACGGACGCCGCGAAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGAGGGCCTTGAGGGCGCTGGTGATGGCGGTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAAAACCTGGATGCGCGAGACGGACGAGGCCGCAACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTACGGCGCCAACTGCGTCACACCGGGGCGCACGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGTGCGGTGACTGCGGCGCCGAGCTGAGCGCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCGCCTTGACGATGAGCTCAGACGTCACCGAACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACACCTGGAGCTGCCCCACGCCGAGGTCACGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCCGAGCTGTCGAAGTGGCGCGCCTATCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCGCCCACCGCATCACCACGTCCCACTGGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGCCGGCCTGGTTCTCAGGCTCTTGTCCTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAGTCTCGCGGGGACTTGCGGATGGCGGCGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAAGCGAGGCCAACCCATCGCAGGGTGCGACCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCCTGGTGCCCGACAGGCGTGATTGCCTGCCACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCTGCCTCTTTCGCGGCCTGTGCTTCGGCTGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACGCCCAGGCATTTTTGTTCGGGCAGATCACCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGCTCGACAAGACGCTGAAAGCAGAGAAGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATCAAGCTCGAAGACAAGCCGCCGTGCCCAAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCCATTTCACCTGGGGAATGGTGATGGTGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGGGGCGGTGACGCGTACCCGTGCACGGGCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGTGAAGGTGCGGTTCGTCCACGAGCCGGGCAACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCTCATGGCTGGTACTCCAGGGTCGTCCCCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCGACTCGACCCATGGTTCGAGCACCCAGCCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAACGACCGAGCACTTGTCGGTCTGCCCGAAAGAGCTACGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCGCCGCGCGGCGATCTTCAACCCCGGGCGGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGTGGCGGCCAGCACCCACCCCATCATCCAGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGTTGCTACGGGTGCAGCGGGAGGCCAATGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTACTCGCGCTCGTCCTCGCCCGGCATCGGCGTCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGTCATCGCGACTGAGGCCGCGCGCCACGTAGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGACGCGTCGGGGAGGAAGAAGTAGGCCCTGCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCTTCGGGAGCGCCACGTCAGTCTGCGCGCGCTGGTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGACCACGAAGGATGCCTGGTTGACGTCCACCGAGTTGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGGACTGGTGGGGCCCGGTGCGGATGTCCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCACCACCCGACCCTTGTCGCGAGCCTGCTTCAGTTTCAACCGACGCTCCCCGCGTTCACGAGGAGCGACACCTCAGCTCTCGACTTCACGGACACCTCCATAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAAGCGTCCGCCGCTGGAGGGGTGCACCGGCCACAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGTCCTCGGCTGGCGTGTCCGCGGCATCGACGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTAAACATCCGCAGCAACTTCATCGTCTTCGACATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCACCACCACGCGCTGGGCGCCCGCGTTCTGTGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGGCAAGGAGTCGGAGGTCGCCACGGTGTTCGGCGCCGTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCATCCAGCACTGGGTGCATCCGAAACGTCACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGCGTTTCTGGTGACGTGCTTGGCGCCTGGGAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACTTCCAGGCGACACACGCGCCGCCACCTACGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACCGTATGCCCAGCTTCCAATCGCGCTGGGCAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGTGCGTGCGCTTGAGGGGCTCACCCACGAAGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCAGCCGGCCCCTGGCGGCGCTCTGTGCGTCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGGTGGCCCGCTGAGCACGGATGGCCAGTGACATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGATTGGGCCAACAGCATTCGGCCTGACACCCACGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCGCAGTACCAAGTGGCCGTCGACTTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTTGCCCCGTTGGAACGCAATGCCCCTCAGCACTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAACCGCCGGGGAGGACTCGGCAAGAGGCAACCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGATTATGTTCATGTCCATGGGAGAGCCTTTGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCGCGGGGCTCATTCAATCACCCCGGCTTTGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGCGAGCAGCGTCTCCATCTCCCCGTAGGTGGCGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGATGACCGGCGCCATCTCGGCAGCCCTGGCCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCACGTGGGGGGCTGTCCTCGGTCAGCAGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGCGACCTTCGAGAGGGACATGCCATTCACATCCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCGCTCATCGGTGGAGACAGGACGAAAGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGGGCAGGGGATGGACGTGGTGACGCCAGCGCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGTGCCGCTACCTCGCTGCCGCGATGAAGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCTCGCGGGCACGCTCGGGTGCGCCACGCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAAGGCCCGGACGGACTACATGGCCGCCTGTGATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCGGAAGGACCGGCCCACGAAGACGCTGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGAACGTGAACTGGGCGGGCAGCTCCGCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACGCGCCAGGCCCGCGAAGGTCCGCACTGCGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGCTTGGGCTTGAACACGTTGCGCGTGAACCGGAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCCGTGCTGTAGCGGCACTCAACCCACTTCAAGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTTCGTGGTTGTGGTGGCCAAGGCCTGCGCTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCAGCGAACGTGTAGAACTCATCCACGTGGGCTCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATGCGATGCAATTCCATGTAAGCATCCTTCCACTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCTTGTCTTCAGCGCTACTCATGGACGAGTCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGGCCATGCGGGGCGTCAATGCCTCCGGGGTCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCGGGCCGCTTCGAGGTGGTGCGCAAGGGCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTACGAGGCGATGGAACAGCCCGCCTTCGTGCGGCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACCTTCACCGGGCTGATCGCGGACAACAGCATCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGACGCCCGAAGTGGATGTGCCGGAGGTGGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGAATGGTGTTCATCGGATGTTGATCCCCGGCTGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGACGCCTAAGGCTGAAGGGGAGGGTGGTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAATTACGCTGCATCAGCACGTCCGTGCGCTAGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGTCGACATCGCAAGCCCGGCGAAGGACAACTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACAAGATCTGGCCGGTGACCCTCCGGGCTCTTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017169|14|1|8784954-8786056|PILER-CR
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CGACGAGCAGGGGTAGGCCGGCGTCCGCCTTGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTATCTGCTGCGGCTGCGGCGGCCTCTGCGACT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CGTTCCACCAGGCGGCAACCTTCACCGTGGTCCG
GTTTCAACCCACGCTCCTCGCGCTCACGAGGAGCGA	CGAGTTCGAGGCACTGCACGACACCTTGCTGCGCA
GTTTCAACCCACGCTCCTCACGTTCACGAGGAGCGA	GCCCATCTTGTAGCGCTTCTCCGTGGGCCGCTT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CGTGGCCTGCGGCCACGGATGACCGGATACGCAGCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTTACGCGGTGGAGCAGGATTTCGCCCCGGCGCTGGC
GTTTCAACCCACGCTCCTCGTGTTCACGAGGAGCGA	CGGTGCCTGGCCCCGCTGGCGTTGAGCCTGTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTCGCCGCGCCTGGGTGTCGTTCCGCCCCTGGTA
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGA	CTGCAGCACTGAGCATGCCGCGCAATCACGACCCCCG
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGA	ATCGCCCGCGTGGTGAGGATTGACGGCGTACCCGTC
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CACTACGCCCGCGTGTTGGACTTGCTCTGCGAGGGG
GTTTCAATCCACGCGCCTCGCGTTCACGAGGAGCGA	CACCGCGTACCTGGACTGGGTGGAGGAGCAGGCCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CCTCCAGGCGGCGCGCCGCGCAACGTTGCGGCTGGT
GTTTCAACCCACGCTCCTCCCGTTCACGAGGAGCGA	CTTGCCCTGCGTCTTCTTCTCGATGCCGCGCCAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTTTTCGAGGGCACGCCGGTTGAGCGGCGCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCTCGACCGGGGCGTCAGCCTCTGCCGCAGCCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTGGGCTGACGTCCAGTCCTGCCTGCTGGCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGCTTCCCCGCAGTCCCAGGAGCACCCCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCTGGCGACCTGCGGCGGCAGAGGGCGGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGCACCCCATGGCCCTCGCCACCGACATGCTGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAAACGCCGGCGGAGGCGCGGCCCCAGGTACATCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGATGGCTTCCCGTGCGCCGGCCAGCGCAATGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCACGTCCGCCGACCGCGAGCGCGCGATGACGTATCTGTTTCAACCCACGATCCCCGCGTTCACGAGGAGCGACAGCTCGCCCACGGACACGCCGGCGGAGCTGGCGCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCTCTGCTGCGGGTGAGTCGCCAGCGCCGGAGTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCAGATGCTGTCTGACGTGTTCGTTGTGGCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGGACGCTTGGGCGGGTCCTGGGGGGCGCCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCTGGAGTGGTAGACACACCCCTTGCAGCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGGCACCTGCTGCGCGAGCGGCGCCACCCCTTGCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCCAGGCTTGGGGGTTGCCGGACGGGTGAAGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGGCAAGTGCCCCGCGGCCCATTCGACAACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCCCAGCAGCCTCGCGCCGTTCATGTTCGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCCCCGGGCATTGTTCGCATCGAGGTGAAGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCCACAGTCCGACTAGCGGGCCGCCTGCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCCCCGGCGCTGGCCGTCCGAAGGGCAGCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGACGACGTAACGGCCATAGCGCAGGTGAAGGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCATCACCGAGCAGCGTCAACTGGTTGCGCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGTCATCGCAGACTGGGGTCAACCTCGTAGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCAAGCTCTGTCGAGCCTGCTTGGTCGGCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCTGTCTTCTCGTCACCGCACGTCGCATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCCATGGCCGCGTTGCGCACGGACGCCGCGAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGGGCCTTGAGGGCGCTGGTGATGGCGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAAACCTGGATGCGCGAGACGGACGAGGCCGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGGCGCCAACTGCGTCACACCGGGGCGCACGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGTGCGGTGACTGCGGCGCCGAGCTGAGCGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCTTGACGATGAGCTCAGACGTCACCGAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACCTGGAGCTGCCCCACGCCGAGGTCACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCGAGCTGTCGAAGTGGCGCGCCTATCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCACCGCATCACCACGTCCCACTGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGCCGGCCTGGTTCTCAGGCTCTTGTCCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTCTCGCGGGGACTTGCGGATGGCGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGAGGCCAACCCATCGCAGGGTGCGACCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCTGGTGCCCGACAGGCGTGATTGCCTGCCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCTGCCTCTTTCGCGGCCTGTGCTTCGGCTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGCCCAGGCATTTTTGTTCGGGCAGATCACC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGCTCGACAAGACGCTGAAAGCAGAGAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCAAGCTCGAAGACAAGCCGCCGTGCCCAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCATTTCACCTGGGGAATGGTGATGGTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGGGCGGTGACGCGTACCCGTGCACGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGAAGGTGCGGTTCGTCCACGAGCCGGGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCTCATGGCTGGTACTCCAGGGTCGTCCCCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGACTCGACCCATGGTTCGAGCACCCAGCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAACGAC	CGAGCACTTGTCGGTCTGCCCGAAAGAGCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCGCCGCGCGGCGATCTTCAACCCCGGGCGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGTGGCGGCCAGCACCCACCCCATCATCCAGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGTTGCTACGGGTGCAGCGGGAGGCCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTACTCGCGCTCGTCCTCGCCCGGCATCGGCGTCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCATCGCGACTGAGGCCGCGCGCCACGTAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGTCGGGGAGGAAGAAGTAGGCCCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTTCGGGAGCGCCACGTCAGTCTGCGCGCGCTG
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CACGAAGGATGCCTGGTTGACGTCCACCGAGTTGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGACTGGTGGGGCCCGGTGCGGATGTCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCACCACCCGACCCTTGTCGCGAGCCTGCTTCA
GTTTCAACCGACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTCAGCTCTCGACTTCACGGACACCTCCATAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGTCCGCCGCTGGAGGGGTGCACCGGCCACAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCCTCGGCTGGCGTGTCCGCGGCATCGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTAAACATCCGCAGCAACTTCATCGTCTTCGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCACCACCACGCGCTGGGCGCCCGCGTTCTGTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGGC	AAGGAGTCGGAGGTCGCCACGGTGTTCGGCGCCGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCATCCAGCACTGGGTGCATCCGAAACGTCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCGTTTCTGGTGACGTGCTTGGCGCCTGGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACTTCCAGGCGACACACGCGCCGCCACCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGTATGCCCAGCTTCCAATCGCGCTGGGCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGCGTGCGCTTGAGGGGCTCACCCACGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCAGCCGGCCCCTGGCGGCGCTCTGTGCGTCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGTGGCCCGCTGAGCACGGATGGCCAGTGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATTGGGCCAACAGCATTCGGCCTGACACCCACGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTGCCCCGTTGGAACGCAATGCCCCTCAGCACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAACCGCCGGGGAGGACTCGGCAAGAGGCAACCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATTATGTTCATGTCCATGGGAGAGCCTTTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGCGGGGCTCATTCAATCACCCCGGCTTTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCGAGCAGCGTCTCCATCTCCCCGTAGGTGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGATGACCGGCGCCATCTCGGCAGCCCTGGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCACGTGGGGGGCTGTCCTCGGTCAGCAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGACCTTCGAGAGGGACATGCCATTCACATCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCTCATCGGTGGAGACAGGACGAAAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGGCAGGGGATGGACGTGGTGACGCCAGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGTGCCGCTACCTCGCTGCCGCGATGAAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGCGGGCACGCTCGGGTGCGCCACGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAGGCCCGGACGGACTACATGGCCGCCTGTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGGAAGGACCGGCCCACGAAGACGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGAACGTGAACTGGGCGGGCAGCTCCGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACGCGCCAGGCCCGCGAAGGTCCGCACTGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCTTGGGCTTGAACACGTTGCGCGTGAACCGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCGTGCTGTAGCGGCACTCAACCCACTTCAAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCGTGGTTGTGGTGGCCAAGGCCTGCGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCAGCGAACGTGTAGAACTCATCCACGTGGGCTCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGCGATGCAATTCCATGTAAGCATCCTTCCACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTTGTCTTCAGCGCTACTCATGGACGAGTCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCCATGCGGGGCGTCAATGCCTCCGGGGTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGGGCCGCTTCGAGGTGGTGCGCAAGGGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGAGGCGATGGAACAGCCCGCCTTCGTGCGGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTTCACCGGGCTGATCGCGGACAACAGCATCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGACGCCCGAAGTGGATGTGCCGGAGGTGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAATGGTGTTCATCGGATGTTGATCCCCGGCTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGACGCCTAAGGCTGAAGGGGAGGGTGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATTACGCTGCATCAGCACGTCCGTGCGCTAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCGACATCGCAAGCCCGGCGAAGGACAACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGATCTGGCCGGTGACCCTCCGGGCTCTTGA


>NZ_CP017169|14|13|8784954-8793564|CRISPRCasFinder
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GACGAGCAGGGGTAGGCCGGCGTCCGCCTTGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TATCTGCTGCGGCTGCGGCGGCCTCTGCGACT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GTTCCACCAGGCGGCAACCTTCACCGTGGTCCG
GTTTCAACCCACGCTCCTCGCGCTCACGAGGAGCGAC	GAGTTCGAGGCACTGCACGACACCTTGCTGCGCA
GTTTCAACCCACGCTCCTCACGTTCACGAGGAGCGAG	CCCATCTTGTAGCGCTTCTCCGTGGGCCGCTT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GTGGCCTGCGGCCACGGATGACCGGATACGCAGCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TTACGCGGTGGAGCAGGATTTCGCCCCGGCGCTGGC
GTTTCAACCCACGCTCCTCGTGTTCACGAGGAGCGAC	GGTGCCTGGCCCCGCTGGCGTTGAGCCTGTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TCGCCGCGCCTGGGTGTCGTTCCGCCCCTGGTA
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGAC	TGCAGCACTGAGCATGCCGCGCAATCACGACCCCCG
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGAA	TCGCCCGCGTGGTGAGGATTGACGGCGTACCCGTC
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACTACGCCCGCGTGTTGGACTTGCTCTGCGAGGGG
GTTTCAATCCACGCGCCTCGCGTTCACGAGGAGCGAC	ACCGCGTACCTGGACTGGGTGGAGGAGCAGGCCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CTCCAGGCGGCGCGCCGCGCAACGTTGCGGCTGGT
GTTTCAACCCACGCTCCTCCCGTTCACGAGGAGCGAC	TTGCCCTGCGTCTTCTTCTCGATGCCGCGCCAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTTTCGAGGGCACGCCGGTTGAGCGGCGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGACCGGGGCGTCAGCCTCTGCCGCAGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTGGGCTGACGTCCAGTCCTGCCTGCTGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCTTCCCCGCAGTCCCAGGAGCACCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCTGGCGACCTGCGGCGGCAGAGGGCGGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGCACCCCATGGCCCTCGCCACCGACATGCTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAACGCCGGCGGAGGCGCGGCCCCAGGTACATCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGGCTTCCCGTGCGCCGGCCAGCGCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCACGTCCGCCGACCGCGAGCGCGCGATGACGTATCT
GTTTCAACCCACGATCCCCGCGTTCACGAGGAGCGAC	AGCTCGCCCACGGACACGCCGGCGGAGCTGGCGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCCTCTGCTGCGGGTGAGTCGCCAGCGCCGGAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCCAGATGCTGTCTGACGTGTTCGTTGTGGCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGGACGCTTGGGCGGGTCCTGGGGGGCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCTGGAGTGGTAGACACACCCCTTGCAGCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCACCTGCTGCGCGAGCGGCGCCACCCCTTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCAGGCTTGGGGGTTGCCGGACGGGTGAAGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGCAAGTGCCCCGCGGCCCATTCGACAACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCCCAGCAGCCTCGCGCCGTTCATGTTCGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCCGGGCATTGTTCGCATCGAGGTGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCACAGTCCGACTAGCGGGCCGCCTGCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCCCCGGCGCTGGCCGTCCGAAGGGCAGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGACGACGTAACGGCCATAGCGCAGGTGAAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCATCACCGAGCAGCGTCAACTGGTTGCGCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGTCATCGCAGACTGGGGTCAACCTCGTAGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCAAGCTCTGTCGAGCCTGCTTGGTCGGCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCTGTCTTCTCGTCACCGCACGTCGCATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCCATGGCCGCGTTGCGCACGGACGCCGCGAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGGGCCTTGAGGGCGCTGGTGATGGCGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAAACCTGGATGCGCGAGACGGACGAGGCCGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGGCGCCAACTGCGTCACACCGGGGCGCACGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGTGCGGTGACTGCGGCGCCGAGCTGAGCGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCTTGACGATGAGCTCAGACGTCACCGAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACCTGGAGCTGCCCCACGCCGAGGTCACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCGAGCTGTCGAAGTGGCGCGCCTATCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCACCGCATCACCACGTCCCACTGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGCCGGCCTGGTTCTCAGGCTCTTGTCCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTCTCGCGGGGACTTGCGGATGGCGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGAGGCCAACCCATCGCAGGGTGCGACCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCTGGTGCCCGACAGGCGTGATTGCCTGCCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCTGCCTCTTTCGCGGCCTGTGCTTCGGCTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGCCCAGGCATTTTTGTTCGGGCAGATCACC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGCTCGACAAGACGCTGAAAGCAGAGAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCAAGCTCGAAGACAAGCCGCCGTGCCCAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCATTTCACCTGGGGAATGGTGATGGTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGGGCGGTGACGCGTACCCGTGCACGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGAAGGTGCGGTTCGTCCACGAGCCGGGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCTCATGGCTGGTACTCCAGGGTCGTCCCCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGACTCGACCCATGGTTCGAGCACCCAGCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAACGAC	CGAGCACTTGTCGGTCTGCCCGAAAGAGCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCGCCGCGCGGCGATCTTCAACCCCGGGCGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGTGGCGGCCAGCACCCACCCCATCATCCAGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGTTGCTACGGGTGCAGCGGGAGGCCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTACTCGCGCTCGTCCTCGCCCGGCATCGGCGTCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCATCGCGACTGAGGCCGCGCGCCACGTAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGTCGGGGAGGAAGAAGTAGGCCCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTTCGGGAGCGCCACGTCAGTCTGCGCGCGCTG
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CACGAAGGATGCCTGGTTGACGTCCACCGAGTTGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGACTGGTGGGGCCCGGTGCGGATGTCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCACCACCCGACCCTTGTCGCGAGCCTGCTTCA
GTTTCAACCGACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTCAGCTCTCGACTTCACGGACACCTCCATAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGTCCGCCGCTGGAGGGGTGCACCGGCCACAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCCTCGGCTGGCGTGTCCGCGGCATCGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTAAACATCCGCAGCAACTTCATCGTCTTCGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCACCACCACGCGCTGGGCGCCCGCGTTCTGTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGGC	AAGGAGTCGGAGGTCGCCACGGTGTTCGGCGCCGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCATCCAGCACTGGGTGCATCCGAAACGTCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCGTTTCTGGTGACGTGCTTGGCGCCTGGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACTTCCAGGCGACACACGCGCCGCCACCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGTATGCCCAGCTTCCAATCGCGCTGGGCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGCGTGCGCTTGAGGGGCTCACCCACGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCAGCCGGCCCCTGGCGGCGCTCTGTGCGTCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGTGGCCCGCTGAGCACGGATGGCCAGTGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATTGGGCCAACAGCATTCGGCCTGACACCCACGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTGCCCCGTTGGAACGCAATGCCCCTCAGCACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAACCGCCGGGGAGGACTCGGCAAGAGGCAACCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATTATGTTCATGTCCATGGGAGAGCCTTTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGCGGGGCTCATTCAATCACCCCGGCTTTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCGAGCAGCGTCTCCATCTCCCCGTAGGTGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGATGACCGGCGCCATCTCGGCAGCCCTGGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCACGTGGGGGGCTGTCCTCGGTCAGCAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGACCTTCGAGAGGGACATGCCATTCACATCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCTCATCGGTGGAGACAGGACGAAAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGGCAGGGGATGGACGTGGTGACGCCAGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGTGCCGCTACCTCGCTGCCGCGATGAAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGCGGGCACGCTCGGGTGCGCCACGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAGGCCCGGACGGACTACATGGCCGCCTGTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGGAAGGACCGGCCCACGAAGACGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGAACGTGAACTGGGCGGGCAGCTCCGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACGCGCCAGGCCCGCGAAGGTCCGCACTGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCTTGGGCTTGAACACGTTGCGCGTGAACCGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCGTGCTGTAGCGGCACTCAACCCACTTCAAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCGTGGTTGTGGTGGCCAAGGCCTGCGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCAGCGAACGTGTAGAACTCATCCACGTGGGCTCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGCGATGCAATTCCATGTAAGCATCCTTCCACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTTGTCTTCAGCGCTACTCATGGACGAGTCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCCATGCGGGGCGTCAATGCCTCCGGGGTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGGGCCGCTTCGAGGTGGTGCGCAAGGGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGAGGCGATGGAACAGCCCGCCTTCGTGCGGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTTCACCGGGCTGATCGCGGACAACAGCATCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGACGCCCGAAGTGGATGTGCCGGAGGTGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAATGGTGTTCATCGGATGTTGATCCCCGGCTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGACGCCTAAGGCTGAAGGGGAGGGTGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATTACGCTGCATCAGCACGTCCGTGCGCTAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCGACATCGCAAGCCCGGCGAAGGACAACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGATCTGGCCGGTGACCCTCCGGGCTCTTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017169|14|2|8784954-8793564|CRT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GACGAGCAGGGGTAGGCCGGCGTCCGCCTTGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TATCTGCTGCGGCTGCGGCGGCCTCTGCGACT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GTTCCACCAGGCGGCAACCTTCACCGTGGTCCG
GTTTCAACCCACGCTCCTCGCGCTCACGAGGAGCGAC	GAGTTCGAGGCACTGCACGACACCTTGCTGCGCA
GTTTCAACCCACGCTCCTCACGTTCACGAGGAGCGAG	CCCATCTTGTAGCGCTTCTCCGTGGGCCGCTT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GTGGCCTGCGGCCACGGATGACCGGATACGCAGCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TTACGCGGTGGAGCAGGATTTCGCCCCGGCGCTGGC
GTTTCAACCCACGCTCCTCGTGTTCACGAGGAGCGAC	GGTGCCTGGCCCCGCTGGCGTTGAGCCTGTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TCGCCGCGCCTGGGTGTCGTTCCGCCCCTGGTA
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGAC	TGCAGCACTGAGCATGCCGCGCAATCACGACCCCCG
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGAA	TCGCCCGCGTGGTGAGGATTGACGGCGTACCCGTC
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACTACGCCCGCGTGTTGGACTTGCTCTGCGAGGGG
GTTTCAATCCACGCGCCTCGCGTTCACGAGGAGCGAC	ACCGCGTACCTGGACTGGGTGGAGGAGCAGGCCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CTCCAGGCGGCGCGCCGCGCAACGTTGCGGCTGGT
GTTTCAACCCACGCTCCTCCCGTTCACGAGGAGCGAC	TTGCCCTGCGTCTTCTTCTCGATGCCGCGCCAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTTTCGAGGGCACGCCGGTTGAGCGGCGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGACCGGGGCGTCAGCCTCTGCCGCAGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTGGGCTGACGTCCAGTCCTGCCTGCTGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCTTCCCCGCAGTCCCAGGAGCACCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCTGGCGACCTGCGGCGGCAGAGGGCGGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGCACCCCATGGCCCTCGCCACCGACATGCTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAACGCCGGCGGAGGCGCGGCCCCAGGTACATCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGGCTTCCCGTGCGCCGGCCAGCGCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCACGTCCGCCGACCGCGAGCGCGCGATGACGTATCT
GTTTCAACCCACGATCCCCGCGTTCACGAGGAGCGAC	AGCTCGCCCACGGACACGCCGGCGGAGCTGGCGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCCTCTGCTGCGGGTGAGTCGCCAGCGCCGGAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCCAGATGCTGTCTGACGTGTTCGTTGTGGCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGGACGCTTGGGCGGGTCCTGGGGGGCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCTGGAGTGGTAGACACACCCCTTGCAGCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCACCTGCTGCGCGAGCGGCGCCACCCCTTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCAGGCTTGGGGGTTGCCGGACGGGTGAAGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGCAAGTGCCCCGCGGCCCATTCGACAACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCCCAGCAGCCTCGCGCCGTTCATGTTCGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCCGGGCATTGTTCGCATCGAGGTGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCACAGTCCGACTAGCGGGCCGCCTGCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCCCCGGCGCTGGCCGTCCGAAGGGCAGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGACGACGTAACGGCCATAGCGCAGGTGAAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCATCACCGAGCAGCGTCAACTGGTTGCGCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGTCATCGCAGACTGGGGTCAACCTCGTAGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCAAGCTCTGTCGAGCCTGCTTGGTCGGCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCTGTCTTCTCGTCACCGCACGTCGCATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCCATGGCCGCGTTGCGCACGGACGCCGCGAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGGGCCTTGAGGGCGCTGGTGATGGCGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAAACCTGGATGCGCGAGACGGACGAGGCCGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGGCGCCAACTGCGTCACACCGGGGCGCACGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGTGCGGTGACTGCGGCGCCGAGCTGAGCGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCTTGACGATGAGCTCAGACGTCACCGAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACCTGGAGCTGCCCCACGCCGAGGTCACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCGAGCTGTCGAAGTGGCGCGCCTATCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCACCGCATCACCACGTCCCACTGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGCCGGCCTGGTTCTCAGGCTCTTGTCCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTCTCGCGGGGACTTGCGGATGGCGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGAGGCCAACCCATCGCAGGGTGCGACCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCTGGTGCCCGACAGGCGTGATTGCCTGCCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCTGCCTCTTTCGCGGCCTGTGCTTCGGCTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGCCCAGGCATTTTTGTTCGGGCAGATCACC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGCTCGACAAGACGCTGAAAGCAGAGAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCAAGCTCGAAGACAAGCCGCCGTGCCCAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCATTTCACCTGGGGAATGGTGATGGTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGGGCGGTGACGCGTACCCGTGCACGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGAAGGTGCGGTTCGTCCACGAGCCGGGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCTCATGGCTGGTACTCCAGGGTCGTCCCCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGACTCGACCCATGGTTCGAGCACCCAGCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAACGAC	CGAGCACTTGTCGGTCTGCCCGAAAGAGCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCGCCGCGCGGCGATCTTCAACCCCGGGCGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGTGGCGGCCAGCACCCACCCCATCATCCAGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGTTGCTACGGGTGCAGCGGGAGGCCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTACTCGCGCTCGTCCTCGCCCGGCATCGGCGTCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCATCGCGACTGAGGCCGCGCGCCACGTAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGTCGGGGAGGAAGAAGTAGGCCCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTTCGGGAGCGCCACGTCAGTCTGCGCGCGCTG
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CACGAAGGATGCCTGGTTGACGTCCACCGAGTTGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGACTGGTGGGGCCCGGTGCGGATGTCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCACCACCCGACCCTTGTCGCGAGCCTGCTTCA
GTTTCAACCGACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTCAGCTCTCGACTTCACGGACACCTCCATAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGTCCGCCGCTGGAGGGGTGCACCGGCCACAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCCTCGGCTGGCGTGTCCGCGGCATCGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTAAACATCCGCAGCAACTTCATCGTCTTCGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCACCACCACGCGCTGGGCGCCCGCGTTCTGTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGGC	AAGGAGTCGGAGGTCGCCACGGTGTTCGGCGCCGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCATCCAGCACTGGGTGCATCCGAAACGTCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCGTTTCTGGTGACGTGCTTGGCGCCTGGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACTTCCAGGCGACACACGCGCCGCCACCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGTATGCCCAGCTTCCAATCGCGCTGGGCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGCGTGCGCTTGAGGGGCTCACCCACGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCAGCCGGCCCCTGGCGGCGCTCTGTGCGTCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGTGGCCCGCTGAGCACGGATGGCCAGTGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATTGGGCCAACAGCATTCGGCCTGACACCCACGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTGCCCCGTTGGAACGCAATGCCCCTCAGCACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAACCGCCGGGGAGGACTCGGCAAGAGGCAACCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATTATGTTCATGTCCATGGGAGAGCCTTTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGCGGGGCTCATTCAATCACCCCGGCTTTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCGAGCAGCGTCTCCATCTCCCCGTAGGTGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGATGACCGGCGCCATCTCGGCAGCCCTGGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCACGTGGGGGGCTGTCCTCGGTCAGCAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGACCTTCGAGAGGGACATGCCATTCACATCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCTCATCGGTGGAGACAGGACGAAAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGGCAGGGGATGGACGTGGTGACGCCAGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGTGCCGCTACCTCGCTGCCGCGATGAAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGCGGGCACGCTCGGGTGCGCCACGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAGGCCCGGACGGACTACATGGCCGCCTGTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGGAAGGACCGGCCCACGAAGACGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGAACGTGAACTGGGCGGGCAGCTCCGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACGCGCCAGGCCCGCGAAGGTCCGCACTGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCTTGGGCTTGAACACGTTGCGCGTGAACCGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCGTGCTGTAGCGGCACTCAACCCACTTCAAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCGTGGTTGTGGTGGCCAAGGCCTGCGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCAGCGAACGTGTAGAACTCATCCACGTGGGCTCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGCGATGCAATTCCATGTAAGCATCCTTCCACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTTGTCTTCAGCGCTACTCATGGACGAGTCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCCATGCGGGGCGTCAATGCCTCCGGGGTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGGGCCGCTTCGAGGTGGTGCGCAAGGGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGAGGCGATGGAACAGCCCGCCTTCGTGCGGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTTCACCGGGCTGATCGCGGACAACAGCATCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGACGCCCGAAGTGGATGTGCCGGAGGTGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAATGGTGTTCATCGGATGTTGATCCCCGGCTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGACGCCTAAGGCTGAAGGGGAGGGTGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATTACGCTGCATCAGCACGTCCGTGCGCTAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCGACATCGCAAGCCCGGCGAAGGACAACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGATCTGGCCGGTGACCCTCCGGGCTCTTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017169|14|2|8787657-8793564|PILER-CR
	CGACGAGCAGGGGTAGGCCGGCGTCCGCCTTGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTATCTGCTGCGGCTGCGGCGGCCTCTGCGACT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CGTTCCACCAGGCGGCAACCTTCACCGTGGTCCG
GTTTCAACCCACGCTCCTCGCGCTCACGAGGAGCGA	CGAGTTCGAGGCACTGCACGACACCTTGCTGCGCA
GTTTCAACCCACGCTCCTCACGTTCACGAGGAGCGA	GCCCATCTTGTAGCGCTTCTCCGTGGGCCGCTT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CGTGGCCTGCGGCCACGGATGACCGGATACGCAGCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTTACGCGGTGGAGCAGGATTTCGCCCCGGCGCTGGC
GTTTCAACCCACGCTCCTCGTGTTCACGAGGAGCGA	CGGTGCCTGGCCCCGCTGGCGTTGAGCCTGTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CTCGCCGCGCCTGGGTGTCGTTCCGCCCCTGGTA
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGA	CTGCAGCACTGAGCATGCCGCGCAATCACGACCCCCG
GTTTCAACCCCCGCTCCTCGCGTTCACGAGGAGCGA	ATCGCCCGCGTGGTGAGGATTGACGGCGTACCCGTC
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CACTACGCCCGCGTGTTGGACTTGCTCTGCGAGGGG
GTTTCAATCCACGCGCCTCGCGTTCACGAGGAGCGA	CACCGCGTACCTGGACTGGGTGGAGGAGCAGGCCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGA	CCTCCAGGCGGCGCGCCGCGCAACGTTGCGGCTGGT
GTTTCAACCCACGCTCCTCCCGTTCACGAGGAGCGA	CTTGCCCTGCGTCTTCTTCTCGATGCCGCGCCAGTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTTTTCGAGGGCACGCCGGTTGAGCGGCGCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCTCGACCGGGGCGTCAGCCTCTGCCGCAGCCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTGGGCTGACGTCCAGTCCTGCCTGCTGGCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGCTTCCCCGCAGTCCCAGGAGCACCCCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCTGGCGACCTGCGGCGGCAGAGGGCGGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGCACCCCATGGCCCTCGCCACCGACATGCTGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAAACGCCGGCGGAGGCGCGGCCCCAGGTACATCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGATGGCTTCCCGTGCGCCGGCCAGCGCAATGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCACGTCCGCCGACCGCGAGCGCGCGATGACGTATCTGTTTCAACCCACGATCCCCGCGTTCACGAGGAGCGACAGCTCGCCCACGGACACGCCGGCGGAGCTGGCGCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCTCTGCTGCGGGTGAGTCGCCAGCGCCGGAGTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCCAGATGCTGTCTGACGTGTTCGTTGTGGCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGGACGCTTGGGCGGGTCCTGGGGGGCGCCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCTGGAGTGGTAGACACACCCCTTGCAGCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGGCACCTGCTGCGCGAGCGGCGCCACCCCTTGCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCCAGGCTTGGGGGTTGCCGGACGGGTGAAGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGGCAAGTGCCCCGCGGCCCATTCGACAACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCCCAGCAGCCTCGCGCCGTTCATGTTCGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCCCCGGGCATTGTTCGCATCGAGGTGAAGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCCACAGTCCGACTAGCGGGCCGCCTGCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGCCCCGGCGCTGGCCGTCCGAAGGGCAGCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGACGACGTAACGGCCATAGCGCAGGTGAAGGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCATCACCGAGCAGCGTCAACTGGTTGCGCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGTCATCGCAGACTGGGGTCAACCTCGTAGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCAAGCTCTGTCGAGCCTGCTTGGTCGGCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCTGTCTTCTCGTCACCGCACGTCGCATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGGCCATGGCCGCGTTGCGCACGGACGCCGCGAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGGGCCTTGAGGGCGCTGGTGATGGCGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAAACCTGGATGCGCGAGACGGACGAGGCCGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGGCGCCAACTGCGTCACACCGGGGCGCACGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGTGCGGTGACTGCGGCGCCGAGCTGAGCGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCTTGACGATGAGCTCAGACGTCACCGAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACCTGGAGCTGCCCCACGCCGAGGTCACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCCGAGCTGTCGAAGTGGCGCGCCTATCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCACCGCATCACCACGTCCCACTGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGCCGGCCTGGTTCTCAGGCTCTTGTCCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTCTCGCGGGGACTTGCGGATGGCGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGAGGCCAACCCATCGCAGGGTGCGACCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCTGGTGCCCGACAGGCGTGATTGCCTGCCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCTGCCTCTTTCGCGGCCTGTGCTTCGGCTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGCCCAGGCATTTTTGTTCGGGCAGATCACC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGCTCGACAAGACGCTGAAAGCAGAGAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCAAGCTCGAAGACAAGCCGCCGTGCCCAAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCATTTCACCTGGGGAATGGTGATGGTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGGGCGGTGACGCGTACCCGTGCACGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGAAGGTGCGGTTCGTCCACGAGCCGGGCAAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCTCATGGCTGGTACTCCAGGGTCGTCCCCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGACTCGACCCATGGTTCGAGCACCCAGCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAACGAC	CGAGCACTTGTCGGTCTGCCCGAAAGAGCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCGCCGCGCGGCGATCTTCAACCCCGGGCGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGTGGCGGCCAGCACCCACCCCATCATCCAGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGTTGCTACGGGTGCAGCGGGAGGCCAATGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTACTCGCGCTCGTCCTCGCCCGGCATCGGCGTCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCATCGCGACTGAGGCCGCGCGCCACGTAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGTCGGGGAGGAAGAAGTAGGCCCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTTCGGGAGCGCCACGTCAGTCTGCGCGCGCTG
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CACGAAGGATGCCTGGTTGACGTCCACCGAGTTGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGACTGGTGGGGCCCGGTGCGGATGTCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCACCACCCGACCCTTGTCGCGAGCCTGCTTCA
GTTTCAACCGACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTCAGCTCTCGACTTCACGGACACCTCCATAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AAGCGTCCGCCGCTGGAGGGGTGCACCGGCCACAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCCTCGGCTGGCGTGTCCGCGGCATCGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTAAACATCCGCAGCAACTTCATCGTCTTCGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCACCACCACGCGCTGGGCGCCCGCGTTCTGTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGGC	AAGGAGTCGGAGGTCGCCACGGTGTTCGGCGCCGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCATCCAGCACTGGGTGCATCCGAAACGTCAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCGTTTCTGGTGACGTGCTTGGCGCCTGGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACTTCCAGGCGACACACGCGCCGCCACCTACG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGTATGCCCAGCTTCCAATCGCGCTGGGCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGTGCGTGCGCTTGAGGGGCTCACCCACGAAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCAGCCGGCCCCTGGCGGCGCTCTGTGCGTCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGGTGGCCCGCTGAGCACGGATGGCCAGTGACAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATTGGGCCAACAGCATTCGGCCTGACACCCACGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTGCCCCGTTGGAACGCAATGCCCCTCAGCACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAACCGCCGGGGAGGACTCGGCAAGAGGCAACCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATTATGTTCATGTCCATGGGAGAGCCTTTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGCGGGGCTCATTCAATCACCCCGGCTTTGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCGAGCAGCGTCTCCATCTCCCCGTAGGTGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGATGACCGGCGCCATCTCGGCAGCCCTGGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCACGTGGGGGGCTGTCCTCGGTCAGCAGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGACCTTCGAGAGGGACATGCCATTCACATCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCTCATCGGTGGAGACAGGACGAAAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGGCAGGGGATGGACGTGGTGACGCCAGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGTGCCGCTACCTCGCTGCCGCGATGAAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTCGCGGGCACGCTCGGGTGCGCCACGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAAGGCCCGGACGGACTACATGGCCGCCTGTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGGAAGGACCGGCCCACGAAGACGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGAACGTGAACTGGGCGGGCAGCTCCGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACGCGCCAGGCCCGCGAAGGTCCGCACTGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCTTGGGCTTGAACACGTTGCGCGTGAACCGGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCCGTGCTGTAGCGGCACTCAACCCACTTCAAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCGTGGTTGTGGTGGCCAAGGCCTGCGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCAGCGAACGTGTAGAACTCATCCACGTGGGCTCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGCGATGCAATTCCATGTAAGCATCCTTCCACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTTGTCTTCAGCGCTACTCATGGACGAGTCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGGCCATGCGGGGCGTCAATGCCTCCGGGGTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGCGGGCCGCTTCGAGGTGGTGCGCAAGGGCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TACGAGGCGATGGAACAGCCCGCCTTCGTGCGGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCTTCACCGGGCTGATCGCGGACAACAGCATCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGACGCCCGAAGTGGATGTGCCGGAGGTGGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAATGGTGTTCATCGGATGTTGATCCCCGGCTGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGACGCCTAAGGCTGAAGGGGAGGGTGGTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATTACGCTGCATCAGCACGTCCGTGCGCTAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTCGACATCGCAAGCCCGGCGAAGGACAACTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGATCTGGCCGGTGACCCTCCGGGCTCTTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017169.1\|WP_140795880.1\|8774204_8775359_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369473
NZ_CP017169.1\|WP_140795894.1\|8802556_8803951_-\|MATE-family-efflux-transporter	unknown	unknown	gnl\|CDD\|240536
NZ_CP017169.1\|WP_140795879.1\|8773473_8774115_+\|TIGR02265-family-protein	unknown	unknown	gnl\|CDD\|131318
NZ_CP017169.1\|WP_140795886.1\|8783825_8784542_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|283403
NZ_CP017169.1\|WP_011556933.1\|8793745_8794036_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP017169.1\|WP_174259087.1\|8804107_8806183_-\|beta-propeller-domain-containing-protein	unknown	unknown	gnl\|CDD\|378255
NZ_CP017169.1\|WP_140800337.1\|8796676_8798419_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	cd09642_cas8c_CAS-I-C	gnl\|CDD\|273839
NZ_CP017169.1\|WP_140795883.1\|8778805_8781103_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_140795888.1\|8795085_8795727_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
NZ_CP017169.1\|WP_140795877.1\|8769017_8771795_-\|TonB-family-protein	unknown	unknown	gnl\|CDD\|367555
NZ_CP017169.1\|WP_140795881.1\|8775804_8776173_+\|response-regulator	unknown	unknown	gnl\|CDD\|381118
NZ_CP017169.1\|WP_140795878.1\|8772459_8772960_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP017169.1\|WP_174259086.1\|8776178_8778578_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017169.1\|WP_140857724.1\|8795723_8796638_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl\|CDD\|274216
NZ_CP017169.1\|WP_174258996.1\|8798418_8799075_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|187534
NZ_CP017169.1\|WP_140795887.1\|8794044_8795073_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP017169.1\|WP_140857720.1\|8781973_8782663_+\|response-regulator	unknown	unknown	gnl\|CDD\|381108
NZ_CP017169.1\|WP_140857726.1\|8799096_8801400_-\|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP017169.1\|WP_140857722.1\|8783194_8783788_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017169.1\|WP_140795893.1\|8801829_8802543_+\|esterase	unknown	unknown	gnl\|CDD\|227283

Protein	Function_ID	Function_description	E-value
NZ_CP017169.1\|WP_140795880.1\|8774204_8775359_-\|hypothetical-protein	gnl\|CDD\|369473	pfam07705, CARDB, CARDB. Cell adhesion related domain found in bacteria.	8.86972e-08
NZ_CP017169.1\|WP_140795894.1\|8802556_8803951_-\|MATE-family-efflux-transporter	gnl\|CDD\|240536	cd13131, MATE_NorM_like, Subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins similar to Vibrio cholerae NorM. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. This subfamily includes Vibrio cholerae NorM and functions most likely as a multidrug efflux pump, removing xenobiotics from the interior of the cell. The pump utilizes a cation gradient across the membrane to facilitate the export process. NorM appears to bind monovalent cations in an outward-facing conformation and may subsequently cycle through an inward-facing and outward-facing conformation to capture and release its substrate.	1.83315e-128
NZ_CP017169.1\|WP_140795879.1\|8773473_8774115_+\|TIGR02265-family-protein	gnl\|CDD\|131318	TIGR02265, Mxa_TIGR02265, Myxococcales-restricted protein, TIGR02265 family. This family consists of a set of at least 17 paralogous proteins in Myxococcus xanthus DK 1622. Members are about 200 amino acids in length. No other homologs are known; the function is unknown.	1.40307e-66
NZ_CP017169.1\|WP_140795886.1\|8783825_8784542_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|283403	pfam05728, UPF0227, Uncharacterized protein family (UPF0227). Despite being classed as uncharacterized proteins, the members of this family are almost certainly enzymes that are distantly related to the pfam00561.	4.70629e-14
NZ_CP017169.1\|WP_011556933.1\|8793745_8794036_-\|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.	5.40072e-27
NZ_CP017169.1\|WP_174259087.1\|8804107_8806183_-\|beta-propeller-domain-containing-protein	gnl\|CDD\|378255	pfam09826, Beta_propel, Beta propeller domain. Members of this family comprise secreted bacterial proteins containing C-terminal beta-propeller domain distantly related to WD-40 repeats. Jpred secondary-structure prediction shows family to be a series of 4 short beta-strands, characteristic of beta-propeller families.	0
NZ_CP017169.1\|WP_140800337.1\|8796676_8798419_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl\|CDD\|273839	TIGR01863, CRISPR-associated_protein_CT1133_family, CRISPR-associated protein Cas8c/Csd1, subtype I-C/DVULG. CRISPR loci appear to be mobile elements with a wide host range. This model represents a protein that tends to be found near CRISPR repeats of the DVULG subtype of CRISPR/Cas locus. We designate this family Csd1 (CRISPR/Cas Subtype DVULG protein 1). The species range for this subtype, so far, is exclusively bacterial and mesophilic, although CRISPR loci in general are particularly common among archaea and thermophilic bacteria. In a few species (Xanthomonas axonopodis pv. citri str. 306 and Streptococcus mutans UA159), homology to this protein family is split across two tandem genes; the trusted cutoff to this family is set low enough to capture at least the longer of the two.	0
NZ_CP017169.1\|WP_140795883.1\|8778805_8781103_+\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.75138e-44
NZ_CP017169.1\|WP_140795888.1\|8795085_8795727_-\|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.	6.91094e-45
NZ_CP017169.1\|WP_140795877.1\|8769017_8771795_-\|TonB-family-protein	gnl\|CDD\|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	8.63396e-14
NZ_CP017169.1\|WP_140795881.1\|8775804_8776173_+\|response-regulator	gnl\|CDD\|381118	cd17580, REC_2_DhkD-like, second phosphoacceptor receiver (REC) domain of Dictyostelium discoideum hybrid signal transduction histidine kinase D and similar domains. Dictyostelium discoideum hybrid signal transduction histidine kinase D (DhkD) is a large protein that contains two histidine kinase (HK) and two REC domains on the intracellular side of a single pass transmembrane domain, and extracellular PAS and PAC domains that likely are involved in ligand binding. This model represents the second REC domain and similar domains. DhkD activates the cAMP phosphodiesterase RegA to ensure proper prestalk and prespore patterning, tip formation, and the vertical elongation of the mound into a finger, in Dictyostelium discoideum. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.23099e-25
NZ_CP017169.1\|WP_140795878.1\|8772459_8772960_-\|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.	5.76104e-11
NZ_CP017169.1\|WP_174259086.1\|8776178_8778578_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.89293e-42
NZ_CP017169.1\|WP_140857724.1\|8795723_8796638_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl\|CDD\|274216	TIGR02589, conserved_hypothetical_protein, CRISPR-associated protein Cas7/Csd2, subtype I-C/DVULG. This model represents one of two closely related CRISPR-associated proteins that belong to the larger family of TIGR01595. Members are the Csd2 protein of the Dvulg subtype of CRISPR/cas system. CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats. The related model is TIGR02590, the Csh2 protein of the Hmari CRISPR subtype.	2.5343e-162
NZ_CP017169.1\|WP_174258996.1\|8798418_8799075_-\|type-I-C-CRISPR-associated-protein-Cas5	gnl\|CDD\|187534	cd09752, Cas5_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas5. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex; in subtype I-C this protein might be the endoribonuclease that generates crRNAs; also known as DevS family.	1.12218e-93
NZ_CP017169.1\|WP_140795887.1\|8794044_8795073_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_CP017169.1\|WP_140857720.1\|8781973_8782663_+\|response-regulator	gnl\|CDD\|381108	cd17557, REC_Rcp-like, phosphoacceptor receiver (REC) domain of cyanobacterial phytochrome response regulator Rcp and similar domains. This family is composed of response regulators (RRs) that are members of phytochrome-associated, light-sensing two-component signal transduction pathways such as Synechocystis sp. Rcp1, Tolypothrix sp. RcpA, and Agrobacterium tumefaciens bacteriophytochrome response regulator AtBRR. They are stand-alone RRs containing only a REC domain with no output/effector domain. The REC domain itself functions as an effector domain. Also included in this family us Methanosaeta harundinacea methanogenesis regulatory protein FilR2, also a stand-alone RR. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.38204e-18
NZ_CP017169.1\|WP_140857726.1\|8799096_8801400_-\|CRISPR-associated-endonuclease-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.	3.43797e-51
NZ_CP017169.1\|WP_140795893.1\|8801829_8802543_+\|esterase	gnl\|CDD\|227283	COG4947, COG4947, Uncharacterized protein conserved in bacteria [Function unknown].	2.41182e-75

>NZ_CP017169.1|WP_140795886.1|8783825_8784542_+|alpha/beta-fold-hydrolase
MSTSTTSPSAVGPRWLYLHGFASGPDSKKGVAVARHYEDQGIPVERLNLRVPSLEQLRLSAMLDTVLAAMGGPEERVVLIGSSLGGLTAARVAEQDARVCALVLLAPAFRVVPQLRRRMGDAAWRHWQTSGWIETDDFVTQQKARIHSGFIADAEAVDARTGGWPDVRVPTLIIHGRQDDTCDVQNSRQWAEGKRHVRLVEVDDGHELTASLPRILEETEVFLQPWGTRGPRAQSSMP
>NZ_CP017169.1|WP_140857722.1|8783194_8783788_+|hypothetical-protein
MRKQSMWVAVVGVLCVGTDAVAAGWNGYASLGAGITLDHLSNFRTKGPALHGYLGLETPPGLSVGLLAEISETWGQQFPDAMRPGQLERSQLDYRAVGIEARLRFFQDKPITPWVGARLSKSWGSTFTPDDVGTWLRQNIDTTSMAFRVGVDGWFSDRWGVSVSTGFQFCDVKLTSNALNQCAKLMQSVIAGPVLRI
>NZ_CP017169.1|WP_140857720.1|8781973_8782663_+|response-regulator
MSRPLQHLLLVEDDLAWRERLTVVAHAEGVKVSHAADGQEALDWLCTRPRASHPDLILLDLLLPRMDGWELYGQLRTNARLRHLGVLMFSGALSGQEPPLDGVVGYLRKPHAPEAADGALRAQLRGLPELPSRDSAEPYALHLPEDVSLPLRTLPGSLSHAVRLHLLRAAELAGTELPLASTWLMALPGTPPSLLVTVDGVQVELEVDDARRRLTVCDVTLSPNLRHGA
>NZ_CP017169.1|WP_140795883.1|8778805_8781103_+|HAMP-domain-containing-protein
MSGRARFAWALVVGLLGHALNRFPVELIPGIDILLGFFLIIPAAPLLGPWCAGLAAGIAMSVTVQMWGHPWSMLGSVMEGVVLGALTRRYWPLQADGIFWLGGIPYLIVSYHLGEDVTATSTFAIAFKQALNSLVPALLTQVVLMTPMARARLWPLLTPALRTFTLSSAVGSALLLALVLPLLMVGTLEGRARYAAERRRMDDQGLSTAHLLAETVDAELSTAQSQTALLASVVMDWWEREGERPPQPQLEELLRDWVYHSAFALNCSIGDSDGSLVAIWPPLGVAAQPVAGSNFADRAYFRDVRSKRAPVVSGVFAGRATVTGPVMVAVAPLLRQQRFEGFTSVAINLPRMRAVAQERLAPGQRALLVDPDGNVAFDTGATPGPEPQSLKGTALGEMLSTLPATGTRTYDTEPQAPPLRRTLGARHLATATLLQPGWRVLVEHPMHDMDFSVIGTYSALLATLALALVLAIPVTRLLTRMLSRPVEAVSHAAGRMAAGERDVRAFGALHHSGAIEVEKLGLAFDEMAARLQRHLEEVERVSQAKAAFFSIASHELKTPLATLKLRLQRLRPDTVRQQDLVLMDRQVDRLARLVNQLLDVSELASGRLSLAQVPLELSALVRRVSERRAASAPQHPLKLSLERVDGWWDEPRLEQVVYNLVDNAIRYSPEGGPVEVVLRREDGDALLEVKDRGVGLGPRGGEELFSRALRGGTLSTISRVEGLGVGLYLSREIITRHGGSIHLAAREGGGTCATVRLPRNDPREA
>NZ_CP017169.1|WP_174259086.1|8776178_8778578_-|PAS-domain-S-box-protein
MSAWEVEVRRIPAAQALPRLALRDGLPRLLEVVASLMRRDSPGGVEDGLGDIPDRHAIERLGEGFDLRQVVTEYRLLRACVLRLWTSRENATHRPEAELVFHEAMDEAVAASVSRYSLARERTLQALDRISTTALGSADAAELLPALLQVLRETVAVVDVAAVLLLEEDVLRVESVVGTGMAVGDVVHMGEGFTGTIAATRQPLLVRAARTDSRVSEPSLRDADLSALFGVPLLLGEQLMGVVLMGSRATHELSEEDQFLFRAMAARTTALLLQAQAHAREREARAVAEASLERLRESEAGLRRWAQVFKRLGVGVAVVDAAEERLREVNPAFARMHGYSPEELTGRRLEDTYAPEARGVLPRHVAVANSKPSHEYESLHIRKDGTRFPAFTHVTAFKDEVGRVVQRVATVVDITQRRAMEMDRQRLLGAIEAERARLASVLDQMPAGVFIADAPSGRLVMASRQVEVITGKPFHPSTSMQDYVEDYGVSLRPDGRPYAMEALPLARSLRHGEVVQGEEMLIPREDGQYVTVLLSSSPIVDREGTIIAAVATMVDVSERRRAQEAALQAVRFGERLIAIVSHDLRNPLNAIQLSATQLLHSEALPERERRLVTRIARSGDRMKRMISELLDFTRGRLGGGIPIQRTAGDLRSVVRLGVDELEAAWPERKLAFRVEPGRYEGEWDEDRLLQVVSNLGGNALQYSPADAPVSFKLYDGGDFVVLEVHNPGEPISPEMLPRLFDPFRRGAMEGVGGGSSSGLGLGLYIVEQVVKGHGGRIEVTSTAQAGTTVRVTLPRLPTG
>NZ_CP017169.1|WP_140795881.1|8775804_8776173_+|response-regulator
MSTPNLVLLVEDHADSRELLEEFLTLEGFTVETAGNGLSAWERLSRPPLPDAVLLDLMMPVMSGWELMRHVREDARLSTLPVVVVSGAGSSQPLPEGIRATVPKPVDLFELRATLERVVSPS
>NZ_CP017169.1|WP_140795880.1|8774204_8775359_-|hypothetical-protein
MTRNHGVSTLTALFLLTGCEGTLPEESPATIDMEVQRQEAKETGLDLSVVDLSASCAATALTLSAAIKNERPTGIGNSTAAVYAGTPGAGGVRLGTISVPWLVGGETFPFSLSYTVPEGTTKVVVVADEDGTYPEDDEDNNFASIDFEIPCATNQQPVASCQSVTVPANAACQGSASIDNGSFDPDGFPGPFSVEQSPAGPYGLGTTSAQLLVSDGAASSTCSANVTVVDVSAPTPGANRGLVIQPVLGSDYVLVPLSDCAMPAVDNCGGELDLDASASIIRVTSDESNDALSLLRLLACDDIKLTPDRKSAMVRAEAALLGNGRVYNFTYAVQDASGNSAIGTCNVKVPALLANPAIDSGVVYCQGDNCPSGSRFPGLLCSLL
>NZ_CP017169.1|WP_140795879.1|8773473_8774115_+|TIGR02265-family-protein
MELRLTPRLVREPAPPQPLGPDAMRELRQRCALATPEDTARGMFFRGVLETVRRVGGSAMEQLCRQSLPEKRYIDFFSYPITQFLPLAFQAAGLLSEHCGGMAAAHRVMGQKAAQDFLESVAGRTLLMLAYDEPRLLLGQLPTGFLAAVSYGERSMVWTGPRSGRFVMKRDFMPTAYHEGVLHAALEAVGARDIGVQGRELGLLDTEYALSWR
>NZ_CP017169.1|WP_140795878.1|8772459_8772960_-|helix-turn-helix-domain-containing-protein
MSLARTHKVDAVKTHLEGPAPPRKRPRPQPRSPADRARKSREQLESRLAESVGEAARGARLLAGLTQADVAERVGIAAEVYGRMERGKMMPSVPTLFRLCLALRLSADVGLGLATAASVGAALWEGDSGHRDQLPEMRKVLRTLRRMSRSQLNLMNQVAAAILPER
>NZ_CP017169.1|WP_140795877.1|8769017_8771795_-|TonB-family-protein
MPGTRAHAQDAGTPEDGGAARAERELQRTDAGWAVETDAPLSEDAGVPEPAFIPPAMVRDSPAPYPPGLASDGVAGVVKLELLIDDAGEVESATLMEGLHPLLDRAALHAAPSLRFAPATLDGLPVAVRIFFEYRFEAPAPGMSEGAAPAAPITLKGLVRTKGNRRPLVGATLVSDAHPDAPVQTDVDGRFEARWPAGVHAVRITAPGHKSGVFREGLKANEALEVVYGLEPLIINPYETVVRGDRERTEVSRVTLHDAELREVPGTMGDPFRVVMLLPGVGSMVSGVAYPVVRGSQPAATGYFLDGIRVPILFHLFLGPAVIHPDFIDAIDFYPGSPPPRYGRLMGGAIDGRLSRPRDDGVHGSAYADLINAGFFIETPFKDTGTNVSLAGRYSYTPWLIALAANQLQAPPPPGRENPKVVLDFWDYQGRVEQRLGEGTLRLFAFGSSDTFGSEAQDEWGDTAMQSIIFHRVDLRHRHPVGPGELEVGGTWGLDRFAIVSRSPPGEATEIHIDQGHWSARLGYTATLSPSATLRAGADVEHKRAIVELLQQDGGSDADVEVAPVALGTFMGAWTELVWQPHEKWAVVPGLRVDSYHLSPGIDRRALEPRLTVRHKVSETLTLKGGAGLFHQPPTTLISLPVVDVGSLLLGLQQGVQLSVGAEWKAWRGLEVGLDVYLNPMLRTLELTPFADEGMVDDDPPDTGTPPAGLRRGMQLGDGGGIPDRSDFDFPDFRSSGMAYGMEFLLRHPLGDNWFGWLSYSLQRSTRRTRFHRYDAEGHRVGEAEADLPFAFDQTHILNLVLSYKFANNITLGGVLHFNTGRPEYGTLGTQTHRPGEDASGRPAWVKADRDRVDRLPAFLRFDVRLSKSWVHDTFSLEAYLDMLNVTLRRETLGFEYEGGNGFPLRKEAVGLPIALPILGVKGRY
>NZ_CP017169.1|WP_011556933.1|8793745_8794036_-|CRISPR-associated-endonuclease-Cas2
MTVLICYDVRVSDPQGPRRLRKIARACRDHGVRVQYSVFECVLEPKDWVVLRARLLGAFDSECDSLRFYFLSEDDARKTEHHGARAPLDVEGPLVL
>NZ_CP017169.1|WP_140795887.1|8794044_8795073_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MTTALNTLFITAEGTRLNKEGECVVVTVQDQKKAEVPLRHLRSVVCLTRAWLTPELMESCLEAGIHVSFFGMTGRFLARVEGVPGGNVLLRRQQYRAADDIARSVAISRALVVGKLGNARQFVLHARRDAAPERQEALSETARRLSEHLRALTRVEDLEQVRGLEGIAARDYFESFPALLKKSAQGFEFDGRNRRPPRNPLNAMLSFGYALLAQDCAGALAGVGLDPAVGFLHEDRPGRLSLALDLMEEFRAPVVDRLVFSLVNRGQLKPGDFRTESAGAVLLKDDARKTFLVAYQEAKQVGVRHAFLGQETTWGMAPHLQSLLLARHLRGELDGYPPFAMR
>NZ_CP017169.1|WP_140795888.1|8795085_8795727_-|CRISPR-associated-protein-Cas4
MSADRETWVALSALQHLLYCERQAALIHVERQWREDVNTASGRLLHERVDLPGHDARVGRRVERAVLLGSQRLRVSGRADMVEYQRDAKGAGWRPYPVEVKRGRRKAGEADRVQLCAQALCLEEMHGVDVPEGALFYGVEHKRAAVRFDAELRQRTEDAIARMHEVLRRQEVPVVVRAPRCDGCSLEPLCLPGVTAGQRSAQDFLARWMDEDG
>NZ_CP017169.1|WP_140857724.1|8795723_8796638_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTDLKQRHDFVLFFDVLDGNPNGDPDAGNLPRIDAETGHGLVTDVSLKRKVRNFILLTQEGKPGLDIFVKEKAILNNRIADAYKSLGIDLNEKPARAEDGKKRNDKGFAQGSEVDKGRAWMCKTFFDVRTFGAVMSTGANAGQVRGPVQLTFARSVDPIVSQEHSITRMAVATEGEAEKQGGDNRTMGRKNTVPYGLYRAHGFVSPHLAKQTGFGPADLELLFQSFTHMFELDRSAARGLMSMRKVVVFKHGSELGNAPAHALFDRVHAVRAQPEKPARSFSDYEVRVDKAGLPQGIEVLELAG
>NZ_CP017169.1|WP_140800337.1|8796676_8798419_-|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MMLTALNDFARERGLTDDPLYETKPVDFFIRVSAAGKFVSLESTAGEDGRGKPLSIPRLPQRSVNIAAGFFADNPKYVLAYEKDAPKAKAGGVEKRVARLDAFLKPVREVAVETKDPEARAVESFLTSEAERRKVLAARDEDEWTGSELLAFVVGDATTPVHQNPAIRACWERRSGEKRALGRTARCLVTGLEGVVALTHPKLKNVPEAQSSGASLVSFNAPAFSSHGLEQGDNAPISQEAALGYVLALNDMLRRTEQRRFRQGIQLGDGSVLVFWTRASPSEESLLLSWMDPTEEDLQRFTESPLHGLQPGALDDRAFYAVTLTGNAGRVAVRDWFESRVGEVKRNIRRYFDDLRIGNAPAGPTPIYRLLNAVEAPSGRGLSPDVATRMVGAALRGLHFPRQLLTSALDRLRLPPADDRFEREQLRLRVALIKATLLRLPRSGTTPLEVTVSLDKNNASQPYVLGRLFAVLERLQGAALKDLNATIRDRYFGAASRNPVTVFPRLLQLSVHHASKAGENGRWLERTKGEVMALLPPERFPRVLGLEDQGLFAVGYYHQREAFFTKRETAASAESDAASS
>NZ_CP017169.1|WP_174258996.1|8798418_8799075_-|type-I-C-CRISPR-associated-protein-Cas5
MASTTGRRFRVRARGPVACFTRPEMKAERVSYEVMTPSAARGVLEAILWKPAIRWHIHEIAVLAPVKWTSFRRNEVNSRATVGRFDYAADEDRAQRNTVALRDVDYVITASFTLLPGKAGPEDNARKFEDMFERRLERGQFFHAPYLGCREFAARVEPAEDGLLPHEAGSGRRPLGLMFYDFVFDVPGAPVRPEFFQAFLEDGVLHVPPRAQVLGGDS
>NZ_CP017169.1|WP_140857726.1|8799096_8801400_-|CRISPR-associated-endonuclease-Cas3''
MQTHVLACAARHVGGGGSAMKKELGLSEQSAVPRVVTAEPLAHVTEDGRPHLLREHLEAVGQWAARLAPREDLRAPALATGRWHDLGKYTQDFWYRIRAENGFEAHLEKEGALERDHSTAGALWSLSRDRRLLPLALAIAGHHAGLPDLAAFKERLGRKEKQALLADARARCDVPALLDGPLGFEPDALVRLEPLRLELWTRMLFSLLCDADFLDTEAFFDASRGSEREVPVTLSQLAERLCGFLDEKQRVAPDTEVNRVRREVLSAAVEAASLHPGVFSLTVPTGGGKTLTSMAFALEHARRHGLQRVIVAIPYTSIIEQSADVYRQAFQGLEHAVIEHHSAVDPEKETALNRVASENWDAPVIVTTTVQLLESLFARRPSACRKLHRVARSVIVLDEAQTLPPSLLAPILDGLGALVKDYDCSVVICTATQPALGRRPDFQEGLPDAREIVPASVRAFERLRRVRVRWPTLGHKLPYTELADAVAAERDVLAVVHLRDDARRLCELVDERLGHQETLHLSALMCPEHRSEVLADIKARKRRGEPVRLVATQLVEAGVDLDFRVVFRGLGGLDSLAQAAGRCNREGLLDGLGELRVYEPETQPPRGVPRAAQDVTRGLLEQAPDLDLFAPASFQRYFERLYATRKLDEKGIQDLRAKLQFDAVSKAFKLVEDDWSASVVVPYANREALLDALRERGPSRERLRALQRFTVTVPRKVREAWLARELARLAAETVAYLGPEHTSAYHERFGLLLDRVGILDPSFLIPG
>NZ_CP017169.1|WP_140795893.1|8801829_8802543_+|esterase
MNREYHRWYSERLHRDMELLIFGHSGEPVLLLPTSKGRFFQAEDFGLIGAIADRVQSGRYIVVCPDSVDEESWFNTAIHPADRVRRHQQWEDYLLHEVVPLLKSRSTGGRLTLAGCSFGGFHSYNIGLRHPHVFRRLLSMGGKFETDEFLDGHHDSDVYFHSCTEWLPNLTDPAQLSALQRVEMVLAVGEHDFCRPSNEHLSNLLWKKDIGNHLSVWQGGTHDWPVWRQMIQQYLPW
>NZ_CP017169.1|WP_140795894.1|8802556_8803951_-|MATE-family-efflux-transporter
MSTAVLPMSSVNSPRTELRELARLAVPIAIAQGGQALMGLVDTLVVGRAGTSALAAVGLGNGLYFAVSSFGIGLMMGFDPMISQAIGARQFTRARALLWQGAWMAFCVGAMLATLMTLAPRLLPLAGISETEAAGASQYLAWRAPGMPMMLMFLTMRSYLQATAFTRPLVIATVVANIFNLLGNLLLVFGGANLPAWFGPLREVPALGVAGSAMATSASIGIELLIAVLFIRSRKVEGAPARRLPVWADLSRAIRLGLPIGLHICAEVGVFALAGVLAAGLGPASVGAHQIAISFASVSFTVAMGIGNAGSVRVGWAVGAHNTPQARLSGFMALAGGAGFMALSGLVFALFPHTLAKLAGAPADVLPLLIPLLMVSAIFQVFDGAQGVGAGVLRGAGDTRFTFLANMVGHYAIGLPVTLLLAFKLGLGVVGIWWGLCAGLISVAVALVWRFNRMSAGTLRPVEA
>NZ_CP017169.1|WP_174259087.1|8804107_8806183_-|beta-propeller-domain-containing-protein
MVAVVAAGCDEGNKPLSPVDNEPVQQEARLESFPGCEALEQHIEDTATKQMRAALESYKQYAYGGGRGGEAPPMTGAPQEDSSGGGGRPNDYTGTNNQVVGVHEADFVQNDGTRIFVLSGPRLYIHRSWPAEQLTRTAALEVEGWPLEMLLDSERNRLVITSGVAEDRPGTVTGGRGTDDMPVIDCAGFGCGYAYSNTVKVTVVDVADLEAPRVLEQIYLPGSYINARRVDSAVRLVFSDGFRWPADVRLYPEYSPGLFDDRGRLVASIDALIKQNEQRIRAQSLEHWLPKGRRVTADGEVKPLAYDCTSFYRANGPTGLGLVSVLSLNLDAEASSPSRTSVVGLPGEVYASHEALYVASRHWWWWPEPGQTTHTYLHKFDIRDPDQATYVGSGTVDGYIVNQFAMDEREGVLRVATTVELPPENPGTGNGGDTAWTPPETVNRVVTLREQDGRLKELGRSEDLARGERIFSARFMGTRGYVVTFRQVDPLFTFDLSDPANPRKVGELKIPGFSTYIHPLGDTHLLTFGEHRNEDGTWQDRALKLSLFDVSDLAQPKETFTHQLGSMGSHSEALYEHKAFTYFPAKGLLALPFTDWDYTAYDYWSGFRSELRVFRVDTATGFSPVGTVSMRDMYQSFNFRNWSWYWQPTVRRSIMADDYVYTISDAGLRVSHVDSLQTPLVTAPFHPPMLP

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP017169_8	8.1\|3469783\|30\|NZ_CP017169\|CRT	3469783-3469812	30	NZ_CP017169.1	3469735-3469764	1	0.967
NZ_CP017169_14	14.94\|8790517\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790517-8790551	35	NZ_CP017169.1	8427797-8427831	1	0.971

1. spacer 8.1|3469783|30|NZ_CP017169|CRT matches to position: 3469735-3469764, mismatch: 1, identity: 0.967

accagggctgatgggagcaccgcctccggc	CRISPR spacer
accagggctgatgggagcaccgccttcggc	Protospacer
*************************.****

2. spacer 14.94|8790517|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to position: 8427797-8427831, mismatch: 1, identity: 0.971

cccaccaccacgcgctgggcgcccgcgttctgtgt	CRISPR spacer
cccaccaccacgcgctgggcgcctgcgttctgtgt	Protospacer
***********************.***********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP017169_14	14.51\|8787481\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8787481-8787514	34	NC_003085	Myxococcus phage Mx8, complete genome	18324-18357	1	0.971
NZ_CP017169_14	14.51\|8787481\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8787481-8787514	34	AF396866	Bacteriophage Mx8, complete genome	18324-18357	1	0.971
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	AY247757	Bacteriophage Mx9 integration region, partial sequence	2921-2955	2	0.943
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	NC_003085	Myxococcus phage Mx8, complete genome	7014-7048	2	0.943
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	AF396866	Bacteriophage Mx8, complete genome	7014-7048	2	0.943
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	U64984	Bacteriophage Mx8 imm, DNA adenine methyltransferase (mox), uoi, and integrase (int) genes, complete cds	7014-7048	2	0.943
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP040452	Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence	1220268-1220293	4	0.846
NZ_CP017169_5	5.1\|1410841\|25\|NZ_CP017169\|CRISPRCasFinder	1410841-1410865	25	NZ_CP029211	Aquabacterium olei strain NBRC 110486 plasmid pTB101, complete sequence	63439-63463	5	0.8
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	205512-205537	5	0.808
NZ_CP017169_14	14.119\|8792285\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792285-8792315	31	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3222873-3222903	5	0.839
NZ_CP017169_8	8.1\|3469783\|30\|NZ_CP017169\|CRT	3469783-3469812	30	MN119376	Streptomyces phage Geostin, complete genome	28793-28822	6	0.8
NZ_CP017169_8	8.1\|3469783\|30\|NZ_CP017169\|CRT	3469783-3469812	30	MH155868	Streptomyces phage FlowerPower, complete genome	28793-28822	6	0.8
NZ_CP017169_8	8.1\|3469783\|30\|NZ_CP017169\|CRT	3469783-3469812	30	MN284894	Streptomyces phage Fabian, complete genome	28793-28822	6	0.8
NZ_CP017169_8	8.3\|3469888\|30\|NZ_CP017169\|CRT	3469888-3469917	30	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	15099-15128	6	0.8
NZ_CP017169_8	8.3\|3469888\|30\|NZ_CP017169\|CRT	3469888-3469917	30	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	362521-362550	6	0.8
NZ_CP017169_11	11.1\|6430072\|26\|NZ_CP017169\|CRISPRCasFinder	6430072-6430097	26	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	1414700-1414725	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP053728	Escherichia coli strain CP61_Sichuan plasmid pCP61-IncN, complete sequence	36265-36290	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP038140	Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence	84300-84325	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP042589	Escherichia coli strain PK6 plasmid pRHEcCUB-1, complete sequence	4454-4479	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	MN816373	Escherichia coli strain A127 plasmid pA127-X1, complete sequence	4454-4479	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	MT219826	Escherichia coli strain RW8-1 plasmid pRW8-1_122k_tetX, complete sequence	34532-34557	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	MT219818	Escherichia coli strain RF148-1 plasmid pRF148-1_119k_tetX, complete sequence	34542-34567	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	MT219823	Escherichia coli strain RF10-1 plasmid pRF10-1_119k_tetX, complete sequence	64623-64648	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP020060	Escherichia coli strain AR_0061 plasmid unitig_2, complete sequence	21378-21403	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP042618	Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-3_MCR3, complete sequence	15213-15238	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP032988	Escherichia coli strain BE2-5 plasmid p2_BE2-5, complete sequence	59912-59937	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP046004	Escherichia coli strain 1919D3 plasmid p1919D3-1, complete sequence	61307-61332	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP033093	Escherichia coli strain CP53 plasmid pCP53-38k, complete sequence	11376-11401	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	NZ_CP041444	Escherichia coli strain YPE10 plasmid pYPE10-78k, complete sequence	24543-24568	6	0.769
NZ_CP017169_11	11.2\|6430126\|26\|NZ_CP017169\|CRISPRCasFinder	6430126-6430151	26	MT219819	Escherichia coli strain RF52-1 plasmid pRF52-1_119k_tetX, complete sequence	8953-8978	6	0.769
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	MH617110	Microviridae sp. isolate ctdb208, complete genome	4154-4185	6	0.812
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP015733	Arthrobacter sp. U41 plasmid unnamed1, complete sequence	19652-19683	6	0.812
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	265339-265369	6	0.806
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP032349	Azospirillum brasilense strain MTCC4039 plasmid p3, complete sequence	385803-385833	6	0.806
NZ_CP017169_14	14.75\|8789166\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789166-8789198	33	NZ_CP013381	Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence	193047-193079	6	0.818
NZ_CP017169_14	14.75\|8789166\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789166-8789198	33	NZ_CP009547	Burkholderia sp. 2002721687 plasmid pBTU, complete sequence	229922-229954	6	0.818
NZ_CP017169_14	14.110\|8791656\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791656-8791689	34	NZ_CP020716	Cnuibacter physcomitrellae strain XA(T) plasmid unnamed1, complete sequence	19674-19707	6	0.824
NZ_CP017169_14	14.111\|8791727\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791727-8791758	32	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	163597-163628	6	0.812
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NC_013860	Azospirillum sp. B510 plasmid pAB510f, complete sequence	175142-175176	6	0.829
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	75447-75481	6	0.829
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NZ_CP029835	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence	14610-14644	6	0.829
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	MH617110	Microviridae sp. isolate ctdb208, complete genome	4154-4186	7	0.788
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	NZ_CP015733	Arthrobacter sp. U41 plasmid unnamed1, complete sequence	19651-19683	7	0.788
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	627923-627959	7	0.811
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	MT711975	Streptomyces phage Alderaan, complete genome	29894-29925	7	0.781
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	627924-627959	7	0.806
NZ_CP017169_14	14.38\|8786555\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8786555-8786587	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1452649-1452681	7	0.788
NZ_CP017169_14	14.38\|8786555\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8786555-8786587	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	360610-360642	7	0.788
NZ_CP017169_14	14.38\|8786555\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8786555-8786587	33	NZ_CP016463	Bosea sp. RAC05 plasmid pBSY19_1, complete sequence	333813-333845	7	0.788
NZ_CP017169_14	14.50\|8787412\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8787412-8787443	32	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	426836-426867	7	0.781
NZ_CP017169_14	14.53\|8787624\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8787624-8787656	33	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	1756272-1756304	7	0.788
NZ_CP017169_14	14.53\|8787624\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8787624-8787656	33	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	32332-32364	7	0.788
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH001457	Streptomyces phage Nesbitt, complete genome	9042-9076	7	0.8
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KT221033	Streptomyces phage SF1, complete genome	8970-9004	7	0.8
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MG593800	Streptomyces phage AbbeyMikolon, complete genome	8970-9004	7	0.8
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP022369	Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence	356360-356390	7	0.774
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	445885-445915	7	0.774
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	312112-312142	7	0.774
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	339754-339784	7	0.774
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	386062-386092	7	0.774
NZ_CP017169_14	14.70\|8788818\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788818-8788850	33	CP000876	Herpetosiphon aurantiacus DSM 785 plasmid pHAU01, complete sequence	137912-137944	7	0.788
NZ_CP017169_14	14.70\|8788818\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788818-8788850	33	MN694437	Marine virus AFVG_250M820, complete genome	25368-25400	7	0.788
NZ_CP017169_14	14.101\|8791015\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791015-8791047	33	MK937607	Gordonia phage Zipp, complete genome	56339-56371	7	0.788
NZ_CP017169_14	14.101\|8791015\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791015-8791047	33	AP014693	Ralstonia phage RSL2 DNA, complete sequence	171362-171394	7	0.788
NZ_CP017169_14	14.116\|8792076\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792076-8792107	32	NZ_CP048282	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence	231471-231502	7	0.781
NZ_CP017169_14	14.118\|8792216\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792216-8792247	32	NC_008712	Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence	136777-136808	7	0.781
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1622051-1622085	7	0.8
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	689716-689748	8	0.758
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	590378-590410	8	0.758
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	590368-590400	8	0.758
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_CP010860	Marinovum algicola DG 898 plasmid pMaD5, complete sequence	104596-104628	8	0.758
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	MT711975	Streptomyces phage Alderaan, complete genome	29894-29926	8	0.758
NZ_CP017169_14	14.4\|8785199\|35\|NZ_CP017169\|PILER-CR	8785199-8785233	35	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	559641-559675	8	0.771
NZ_CP017169_14	14.4\|8785199\|35\|NZ_CP017169\|PILER-CR	8785199-8785233	35	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	488890-488924	8	0.771
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	91950-91986	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	518229-518265	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	529957-529993	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1386972-1387008	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	533045-533081	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	188559-188595	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	538073-538109	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	1535314-1535350	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	534308-534344	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1644981-1645017	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	545779-545815	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	531433-531469	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	432080-432116	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	530527-530563	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	537055-537091	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1457995-1458031	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	534325-534361	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	540340-540376	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	550448-550484	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	528479-528515	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	540340-540376	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	528483-528519	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	540340-540376	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	540340-540376	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	540340-540376	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	1563565-1563601	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	528483-528519	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	545762-545798	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	545715-545751	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	580145-580181	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	537539-537575	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	538851-538887	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	528483-528519	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	550447-550483	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	528483-528519	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	528483-528519	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	540342-540378	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	1535007-1535043	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	550450-550486	8	0.784
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	1535007-1535043	8	0.784
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1429980-1430011	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1237465-1237496	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP033202	Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence	10561-10592	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP003988	Streptomyces sp. 769 plasmid pSGZL, complete sequence	99313-99344	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	KY471269	Gordonia phage DinoDaryn, complete genome	2452-2483	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	KY471268	Gordonia phage Huffy, complete genome	2452-2483	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP013369	Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence	249278-249309	8	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP010607	Phaeobacter inhibens strain P83 plasmid pP83_h, complete sequence	1920-1951	8	0.75
NZ_CP017169_14	14.18\|8785130\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8785130-8785162	33	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	494337-494369	8	0.758
NZ_CP017169_14	14.19\|8785200\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8785200-8785233	34	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	559641-559674	8	0.765
NZ_CP017169_14	14.19\|8785200\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8785200-8785233	34	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	488891-488924	8	0.765
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	518230-518265	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	529958-529993	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	533046-533081	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	188560-188595	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	538074-538109	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	1535315-1535350	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	534309-534344	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	545780-545815	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	531434-531469	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	432081-432116	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	530528-530563	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	534326-534361	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	540341-540376	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	550449-550484	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	528480-528515	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	540341-540376	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	528484-528519	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	540341-540376	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	540341-540376	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	540341-540376	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	528484-528519	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	545763-545798	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	545716-545751	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	580146-580181	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	537540-537575	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	538852-538887	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	528484-528519	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	550448-550483	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	528484-528519	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	528484-528519	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	540343-540378	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	550451-550486	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	91950-91985	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1386972-1387007	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1644981-1645016	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	537055-537090	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1457995-1458030	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	1563565-1563600	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	1535007-1535042	8	0.778
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	1535007-1535042	8	0.778
NZ_CP017169_14	14.33\|8786200\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8786200-8786233	34	MN961670	Pseudomonas putida strain 420352 plasmid p420352-IMP, complete sequence	391504-391537	8	0.765
NZ_CP017169_14	14.63\|8788333\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788333-8788364	32	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	544344-544375	8	0.75
NZ_CP017169_14	14.63\|8788333\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788333-8788364	32	MH744418	Streptomyces phage JustBecause, complete genome	140757-140788	8	0.75
NZ_CP017169_14	14.63\|8788333\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788333-8788364	32	MT310898	Streptomyces phage Kela, complete genome	141340-141371	8	0.75
NZ_CP017169_14	14.64\|8788402\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788402-8788432	31	NZ_CP020399	Burkholderia multivorans strain FDAARGOS_246 plasmid unnamed, complete sequence	86391-86421	8	0.742
NZ_CP017169_14	14.65\|8788470\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788470-8788502	33	NZ_CP007515	Rubrobacter radiotolerans strain RSPS-4 plasmid 1, complete sequence	89437-89469	8	0.758
NZ_CP017169_14	14.65\|8788470\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788470-8788502	33	NZ_CP007517	Rubrobacter radiotolerans strain RSPS-4 plasmid 3, complete sequence	43282-43314	8	0.758
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	765508-765539	8	0.75
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	1311811-1311842	8	0.75
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	263969-264002	8	0.765
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	263969-264002	8	0.765
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	263981-264014	8	0.765
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	264002-264035	8	0.765
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	263968-264001	8	0.765
NZ_CP017169_14	14.81\|8789591\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789591-8789624	34	NZ_CP038140	Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence	36961-36994	8	0.765
NZ_CP017169_14	14.81\|8789591\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789591-8789624	34	NZ_CP038140	Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence	41561-41594	8	0.765
NZ_CP017169_14	14.88\|8790092\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790092-8790123	32	NZ_CP024582	Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence	32009-32040	8	0.75
NZ_CP017169_14	14.88\|8790092\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790092-8790123	32	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	396255-396286	8	0.75
NZ_CP017169_14	14.89\|8790161\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790161-8790193	33	NZ_CP034394	Herbaspirillum seropedicae strain AU13965 plasmid unnamed, complete sequence	25317-25349	8	0.758
NZ_CP017169_14	14.92\|8790374\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790374-8790407	34	NZ_LR134447	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 5, complete sequence	246656-246689	8	0.765
NZ_CP017169_14	14.110\|8791656\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791656-8791689	34	MG812496	Gordonia phage SallySpecial, complete genome	9376-9409	8	0.765
NZ_CP017169_14	14.116\|8792076\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792076-8792107	32	NZ_CP019037	Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence	113569-113600	8	0.75
NZ_CP017169_14	14.119\|8792285\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792285-8792315	31	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	358017-358047	8	0.742
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NC_019339	Arthrobacter sp. J3-49 plasmid pJ349-116, complete sequence	27867-27901	8	0.771
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	1369832-1369864	9	0.727
NZ_CP017169_8	8.3\|3469888\|30\|NZ_CP017169\|CRT	3469888-3469917	30	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	15078-15107	9	0.7
NZ_CP017169_8	8.3\|3469888\|30\|NZ_CP017169\|CRT	3469888-3469917	30	NZ_CP021083	Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence	229435-229464	9	0.7
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1237465-1237497	9	0.727
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	NZ_CP033202	Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence	10561-10593	9	0.727
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1429979-1430011	9	0.727
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	NZ_CP003988	Streptomyces sp. 769 plasmid pSGZL, complete sequence	99312-99344	9	0.727
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	KY471269	Gordonia phage DinoDaryn, complete genome	2451-2483	9	0.727
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	KY471268	Gordonia phage Huffy, complete genome	2451-2483	9	0.727
NZ_CP017169_14	14.3\|8785129\|34\|NZ_CP017169\|PILER-CR	8785129-8785162	34	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	494337-494370	9	0.735
NZ_CP017169_14	14.9\|8785554\|34\|NZ_CP017169\|PILER-CR	8785554-8785587	34	NZ_CP049359	Deinococcus wulumuqiensis R12 plasmid unnamed2, complete sequence	65727-65760	9	0.735
NZ_CP017169_14	14.9\|8785554\|34\|NZ_CP017169\|PILER-CR	8785554-8785587	34	NZ_CP031160	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence	19979-20012	9	0.735
NZ_CP017169_14	14.13\|8785841\|36\|NZ_CP017169\|PILER-CR	8785841-8785876	36	MK388689	Pantoea phage vB_PagM_LIET2, complete genome	26402-26437	9	0.75
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP007648	Lactobacillus salivarius strain JCM1046 plasmid pMP1046B, complete sequence	91892-91923	9	0.719
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP023509	Rothia mucilaginosa strain FDAARGOS_369 plasmid unnamed, complete sequence	13369-13400	9	0.719
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	371029-371060	9	0.719
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP025513	Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence	234999-235030	9	0.719
NZ_CP017169_14	14.22\|8785412\|36\|NZ_CP017169\|CRISPRCasFinder,CRT	8785412-8785447	36	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	412156-412191	9	0.75
NZ_CP017169_14	14.24\|8785555\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8785555-8785587	33	NZ_CP031160	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence	19979-20011	9	0.727
NZ_CP017169_14	14.24\|8785555\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8785555-8785587	33	NZ_CP049359	Deinococcus wulumuqiensis R12 plasmid unnamed2, complete sequence	65728-65760	9	0.727
NZ_CP017169_14	14.34\|8786271\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8786271-8786302	32	NZ_CP016024	Ralstonia insidiosa strain ATCC 49129 plasmid pRI-1, complete sequence	42090-42121	9	0.719
NZ_CP017169_14	14.49\|8787342\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8787342-8787374	33	NC_008308	Sphingomonas sp. KA1 plasmid pCAR3 DNA, complete sequence	153789-153821	9	0.727
NZ_CP017169_14	14.51\|8787481\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8787481-8787514	34	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	157438-157471	9	0.735
NZ_CP017169_14	14.63\|8788333\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788333-8788364	32	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	136246-136277	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	KU985096	Mycobacterium phage Kazan, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MG099952	Mycobacterium phage WunderPhul, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MK359352	Mycobacterium phage JewelBug, complete genome	3147-3178	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	KX375815	Mycobacterium phage ToneTone, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MK494090	Mycobacterium phage Jordennis, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	KX641261	Mycobacterium phage Isiphiwo, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	KF560333	Mycobacterium phage Artemis2UCLA, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	KU695582	Mycobacterium phage McFly, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MT024861	Mycobacterium phage Pmask, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MH155876	Mycobacterium phage Priamo, complete genome	3161-3192	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MK359360	Mycobacterium phage Hexamo, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MH051253	Mycobacterium phage GreedyLawyer, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MT657338	Mycobacterium phage SuperCallie99, complete genome	3147-3178	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NC_042334	Mycobacterium virus Jeffabunny, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MN728683	Mycobacterium phage Yokurt, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NC_022965	Mycobacterium phage CloudWang3, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	JF937092	Mycobacterium phage DaVinci, complete genome	3147-3178	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MF668288	Mycobacterium phage Wiks, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MH020240	Mycobacterium phage SuperAwesome, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MG099945	Mycobacterium phage Koko, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MK894433	Mycobacterium phage Kipper29, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NC_022985	Mycobacterium phage Zaka, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	JN049605	Mycobacterium virus EricB, complete genome	3147-3178	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MN586039	Mycobacterium phage Blinn1, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	MH779517	Mycobacterium phage Zulu, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.73\|8789027\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789027-8789058	32	NC_029077	Mycobacterium phage VohminGhazi, complete genome	3146-3177	9	0.719
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP023017	Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence	247364-247397	9	0.735
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	257193-257226	9	0.735
NZ_CP017169_14	14.76\|8789236\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789236-8789269	34	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	257182-257215	9	0.735
NZ_CP017169_14	14.83\|8789732\|36\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789732-8789767	36	NZ_CP022666	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence	220649-220684	9	0.75
NZ_CP017169_14	14.83\|8789732\|36\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789732-8789767	36	NZ_CP050086	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence	1031755-1031790	9	0.75
NZ_CP017169_14	14.88\|8790092\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790092-8790123	32	NC_017966	Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence	62615-62646	9	0.719
NZ_CP017169_14	14.95\|8790589\|36\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790589-8790624	36	NZ_CP009405	Mycobacterium avium subsp. hominissuis strain OCU464 plasmid p78K, complete sequence	35423-35458	9	0.75
NZ_CP017169_14	14.111\|8791727\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791727-8791758	32	NC_023283	Streptomyces sp. FR1 plasmid pFRL3, complete sequence	334676-334707	9	0.719
NZ_CP017169_14	14.119\|8792285\|31\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792285-8792315	31	NC_047866	Aeromonas phage Ahp1, complete genome	16734-16764	9	0.71
NZ_CP017169_14	14.120\|8792353\|33\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792353-8792385	33	NZ_CP026221	Aeromonas sp. ASNIH4 plasmid pAER-f909, complete sequence	78656-78688	9	0.727
NZ_CP017169_14	14.128\|8792924\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792924-8792958	35	NZ_CP032678	Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence	504368-504402	9	0.743
NZ_CP017169_14	14.129\|8792996\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792996-8793030	35	MG710528	Escherichia phage GER2, complete genome	73867-73901	9	0.743
NZ_CP017169_14	14.129\|8792996\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792996-8793030	35	NC_008464	Stx2-converting phage 86, complete genome	30678-30712	9	0.743
NZ_CP017169_14	14.129\|8792996\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8792996-8793030	35	AB255436	Stx2-converting phage 86 DNA, complete genome	30678-30712	9	0.743
NZ_CP017169_14	14.133\|8793284\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8793284-8793315	32	NC_014819	Asticcacaulis excentricus CB 48 plasmid pASTEX02, complete sequence	157983-158014	9	0.719
NZ_CP017169_14	14.136\|8793494\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8793494-8793527	34	NZ_CP017422	Arthrobacter sp. ZXY-2 plasmid pZXY21, complete sequence	247543-247576	9	0.735
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NC_006462	Thermus thermophilus HB8 plasmid pTT27, complete sequence	130543-130575	10	0.697
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NC_017273	Thermus thermophilus SG0.5JP17-16 plasmid pTHTHE1601, complete sequence	217821-217853	10	0.697
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_AP019802	Thermus thermophilus strain HC11 plasmid pHC11, complete sequence	257602-257634	10	0.697
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NC_017588	Thermus thermophilus JL-18 plasmid pTTJL1801, complete sequence	5983-6015	10	0.697
NZ_CP017169_2	2.1\|654742\|33\|NZ_CP017169\|CRISPRCasFinder	654742-654774	33	NZ_LR027520	Thermus thermophilus isolate TTHNAR1 plasmid 4, complete sequence	125503-125535	10	0.697
NZ_CP017169_14	14.8\|8785484\|34\|NZ_CP017169\|PILER-CR	8785484-8785517	34	NZ_CP046573	Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence	131786-131819	10	0.706
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP032520	Cupriavidus oxalaticus strain T2 plasmid unnamed1, complete sequence	232157-232188	10	0.688
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP040765	Paracoccus sp. 2251 plasmid unnamed1, complete sequence	18915-18946	10	0.688
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	219368-219399	10	0.688
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	741074-741105	10	0.688
NZ_CP017169_14	14.17\|8785061\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785061-8785092	32	MK240575	Thermobifida phage P318, complete genome	24234-24265	10	0.688
NZ_CP017169_14	14.20\|8785271\|32\|NZ_CP017169\|CRISPRCasFinder,CRT	8785271-8785302	32	NC_020548	Azoarcus sp. KH32C plasmid pAZKH, complete sequence	574368-574399	10	0.688
NZ_CP017169_14	14.23\|8785485\|33\|NZ_CP017169\|CRISPRCasFinder,CRT	8785485-8785517	33	NZ_CP046573	Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence	131786-131818	10	0.697
NZ_CP017169_14	14.28\|8785842\|35\|NZ_CP017169\|CRISPRCasFinder,CRT	8785842-8785876	35	MK388689	Pantoea phage vB_PagM_LIET2, complete genome	26402-26436	10	0.714
NZ_CP017169_14	14.42\|8786844\|34\|NZ_CP017169\|CRISPRCasFinder,CRT	8786844-8786877	34	NZ_CP039433	Rhodococcus sp. SGAir0479 plasmid unnamed	26811-26844	10	0.706
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN284893	Mycobacterium phage LilMcDreamy, complete genome	23898-23932	10	0.714
NZ_CP017169_14	14.66\|8788540\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788540-8788571	32	NZ_CP014308	Burkholderia sp. PAMC 26561 plasmid unnamed1, complete sequence	495268-495299	10	0.688
NZ_CP017169_14	14.66\|8788540\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788540-8788571	32	NZ_CP014309	Burkholderia sp. PAMC 26561 plasmid unnamed2, complete sequence	339826-339857	10	0.688
NZ_CP017169_14	14.81\|8789591\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789591-8789624	34	NZ_CP027025	Streptomyces sp. WAC00288 plasmid p3, complete sequence	13227-13260	10	0.706
NZ_CP017169_14	14.81\|8789591\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8789591-8789624	34	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	504040-504073	10	0.706
NZ_CP017169_14	14.130\|8793068\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8793068-8793102	35	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	533828-533862	10	0.714
NZ_CP017169_14	14.2\|8785060\|33\|NZ_CP017169\|PILER-CR	8785060-8785092	33	NZ_CP032520	Cupriavidus oxalaticus strain T2 plasmid unnamed1, complete sequence	232157-232189	11	0.667
NZ_CP017169_14	14.7\|8785411\|37\|NZ_CP017169\|PILER-CR	8785411-8785447	37	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	412156-412192	11	0.703
NZ_CP017169_14	14.30\|8785986\|35\|NZ_CP017169\|CRISPRCasFinder,CRT	8785986-8786020	35	NZ_LR723671	Rhizobium flavum strain YW14 plasmid 2	92062-92096	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MG812490	Mycobacterium phage Holeinone, complete genome	25022-25056	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH051249	Mycobacterium phage Boyle, complete genome	25151-25185	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN428049	Mycobacterium phage West99, complete genome	25154-25188	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN586045	Mycobacterium phage Brownie5, complete genome	25160-25194	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH001452	Mycobacterium phage Kheth, complete genome	25039-25073	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH697584	Mycobacterium phage FrenchFry, complete genome	25157-25191	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN813678	Mycobacterium phage Lephleur, complete genome	25040-25074	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MG757162	Mycobacterium phage Opia, complete genome	25027-25061	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MK814751	Mycobacterium phage Bananafish, complete genome	25032-25066	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KT365402	Mycobacterium phage Tres, complete genome	25037-25071	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KM101117	Mycobacterium phage LizLemon, complete genome	25147-25181	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	JN698991	Mycobacterium phage Hedgerow, complete genome	25139-25173	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	NC_043767	Mycobacterium virus TA17a, complete genome	25021-25055	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN586046	Mycobacterium phage Tinciduntsolum, complete genome	25159-25193	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MT639652	Mycobacterium phage MasterPo, complete genome	25040-25074	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MK620898	Mycobacterium phage Coffee, complete genome	25143-25177	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	JN699004	Mycobacterium phage Ares, complete genome	25040-25074	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MG812491	Mycobacterium phage ItsyBitsy1, complete genome	25021-25055	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MN234225	Mycobacterium phage Rhinoforte, complete genome	25147-25181	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	DQ398048	Mycobacterium phage Qyrzula, complete genome	25122-25156	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KR997932	Mycobacterium phage Godines, complete genome	25040-25074	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	AY129334	Mycobacterium phage Rosebush, complete genome	25154-25188	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH590591	Mycobacterium phage Sabella, complete genome	25034-25068	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	JN618996	Mycobacterium phage Arbiter, complete genome	25115-25149	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KX443696	Mycobacterium phage Laurie, complete genome	25034-25068	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MH727546	Mycobacterium phage Eaglehorse, complete genome	25061-25095	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	MK061411	Mycobacterium phage Faze9, complete genome	25157-25191	11	0.686
NZ_CP017169_14	14.58\|8787976\|35\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8787976-8788010	35	KT880194	Mycobacterium phage Glass, complete genome	25157-25191	11	0.686
NZ_CP017169_14	14.66\|8788540\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8788540-8788571	32	NZ_LR027520	Thermus thermophilus isolate TTHNAR1 plasmid 4, complete sequence	8543-8574	11	0.656
NZ_CP017169_14	14.92\|8790374\|34\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8790374-8790407	34	NZ_CP026189	Enterobacteriaceae bacterium ENNIH2 plasmid pENT-812c, complete sequence	56029-56062	11	0.676
NZ_CP017169_14	14.111\|8791727\|32\|NZ_CP017169\|CRISPRCasFinder,CRT,PILER-CR	8791727-8791758	32	NZ_CP016082	Streptomyces sp. SAT1 plasmid unnamed2, complete sequence	263959-263990	11	0.656

1. spacer 14.51|8787481|34|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_003085 (Myxococcus phage Mx8, complete genome) position: , mismatch: 1, identity: 0.971

cgcgccccggcgctggccgtccgaagggcagccg	CRISPR spacer
cacgccccggcgctggccgtccgaagggcagccg	Protospacer
*.********************************

2. spacer 14.51|8787481|34|NZ_CP017169|CRISPRCasFinder,CRT matches to AF396866 (Bacteriophage Mx8, complete genome) position: , mismatch: 1, identity: 0.971

cgcgccccggcgctggccgtccgaagggcagccg	CRISPR spacer
cacgccccggcgctggccgtccgaagggcagccg	Protospacer
*.********************************

3. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to AY247757 (Bacteriophage Mx9 integration region, partial sequence) position: , mismatch: 2, identity: 0.943

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
cgcgagggccttgagggcgccggtgatggcggcga	Protospacer
********************.***********.**

4. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_003085 (Myxococcus phage Mx8, complete genome) position: , mismatch: 2, identity: 0.943

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
cgcgagggccttgagggcgccggtgatggcagtga	Protospacer
********************.*********.****

5. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to AF396866 (Bacteriophage Mx8, complete genome) position: , mismatch: 2, identity: 0.943

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
cgcgagggccttgagggcgccggtgatggcagtga	Protospacer
********************.*********.****

6. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to U64984 (Bacteriophage Mx8 imm, DNA adenine methyltransferase (mox), uoi, and integrase (int) genes, complete cds) position: , mismatch: 2, identity: 0.943

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
cgcgagggccttgagggcgccggtgatggcagtga	Protospacer
********************.*********.****

7. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP040452 (Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence) position: , mismatch: 4, identity: 0.846

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
tgcgctgaccatcagaacgcctgaca	Protospacer
.******* *********** ****.

8. spacer 5.1|1410841|25|NZ_CP017169|CRISPRCasFinder matches to NZ_CP029211 (Aquabacterium olei strain NBRC 110486 plasmid pTB101, complete sequence) position: , mismatch: 5, identity: 0.8

cttggcctgcgtgcggggtgattcg	CRISPR spacer
gatgtcctgcgtgcggggtgattgc	Protospacer
  ** ******************

9. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 5, identity: 0.808

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
cacgctgatcatcagaacgcgtgtgc	Protospacer
*.****** **************

10. spacer 14.119|8792285|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 5, identity: 0.839

cggaacg-tgaactgggcgggcagctccgcga	CRISPR spacer
-ggaccgctggactgggcggtcagctccgcgc	Protospacer
 *** ** **.********* **********

11. spacer 8.1|3469783|30|NZ_CP017169|CRT matches to MN119376 (Streptomyces phage Geostin, complete genome) position: , mismatch: 6, identity: 0.8

accagggctgatgggagcaccgcctccggc	CRISPR spacer
cccagggctgtggggagcaccgcctacatc	Protospacer
 *********  ************* *. *

12. spacer 8.1|3469783|30|NZ_CP017169|CRT matches to MH155868 (Streptomyces phage FlowerPower, complete genome) position: , mismatch: 6, identity: 0.8

accagggctgatgggagcaccgcctccggc	CRISPR spacer
cccagggctgtggggagcaccgcctacatc	Protospacer
 *********  ************* *. *

13. spacer 8.1|3469783|30|NZ_CP017169|CRT matches to MN284894 (Streptomyces phage Fabian, complete genome) position: , mismatch: 6, identity: 0.8

accagggctgatgggagcaccgcctccggc	CRISPR spacer
cccagggctgtggggagcaccgcctacatc	Protospacer
 *********  ************* *. *

14. spacer 8.3|3469888|30|NZ_CP017169|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 6, identity: 0.8

gatgggcgggcaggctcctgcgacggctgg	CRISPR spacer
ccggggcgggcagggtccggcgacggctgt	Protospacer
   *********** *** **********

15. spacer 8.3|3469888|30|NZ_CP017169|CRT matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 6, identity: 0.8

gatgg-gcgggcaggctcctgcgacggctgg	CRISPR spacer
-atgacacgggcatgctcctgcgaaggctgc	Protospacer
 ***. .****** ********** *****

16. spacer 11.1|6430072|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 6, identity: 0.769

agcgctgggcgttggaacgcgcgacg	CRISPR spacer
ggcgctgggcgatggaacgcgccgtc	Protospacer
.********** ********** ..

17. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP053728 (Escherichia coli strain CP61_Sichuan plasmid pCP61-IncN, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

18. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP038140 (Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

19. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP042589 (Escherichia coli strain PK6 plasmid pRHEcCUB-1, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

20. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to MN816373 (Escherichia coli strain A127 plasmid pA127-X1, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

21. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to MT219826 (Escherichia coli strain RW8-1 plasmid pRW8-1_122k_tetX, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

22. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to MT219818 (Escherichia coli strain RF148-1 plasmid pRF148-1_119k_tetX, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

23. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to MT219823 (Escherichia coli strain RF10-1 plasmid pRF10-1_119k_tetX, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

24. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP020060 (Escherichia coli strain AR_0061 plasmid unitig_2, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

25. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP042618 (Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-3_MCR3, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

26. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP032988 (Escherichia coli strain BE2-5 plasmid p2_BE2-5, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

27. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP046004 (Escherichia coli strain 1919D3 plasmid p1919D3-1, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

28. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP033093 (Escherichia coli strain CP53 plasmid pCP53-38k, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

29. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to NZ_CP041444 (Escherichia coli strain YPE10 plasmid pYPE10-78k, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

30. spacer 11.2|6430126|26|NZ_CP017169|CRISPRCasFinder matches to MT219819 (Escherichia coli strain RF52-1 plasmid pRF52-1_119k_tetX, complete sequence) position: , mismatch: 6, identity: 0.769

cgcgctgagcatcagaacgcgtgacg	CRISPR spacer
gtaactgagcatcagatcgcgtgaca	Protospacer
   .************ ********.

31. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to MH617110 (Microviridae sp. isolate ctdb208, complete genome) position: , mismatch: 6, identity: 0.812

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ttcctgctgcggccgcggccgcctctgcgata	Protospacer
* .**********.***** **********.

32. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP015733 (Arthrobacter sp. U41 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.812

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
cgtctgctgcggctgcggcggccccggccgct	Protospacer
..*********************.* ** .**

33. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.806

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgccgtcttc	Protospacer
*****************.* *****  ..**

34. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032349 (Azospirillum brasilense strain MTCC4039 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.806

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgccgccttc	Protospacer
*****************.* *****  ..**

35. spacer 14.75|8789166|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013381 (Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence) position: , mismatch: 6, identity: 0.818

gtggggc-ggtgacgcgtacccgtgcacgggcgg	CRISPR spacer
-tggtccgggtgacgcgtacccgcgcactggcgc	Protospacer
 ***  * ***************.**** ****

36. spacer 14.75|8789166|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009547 (Burkholderia sp. 2002721687 plasmid pBTU, complete sequence) position: , mismatch: 6, identity: 0.818

gtggggc-ggtgacgcgtacccgtgcacgggcgg	CRISPR spacer
-tggtccgggtgacgcgtacccgcgcactggcgc	Protospacer
 ***  * ***************.**** ****

37. spacer 14.110|8791656|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020716 (Cnuibacter physcomitrellae strain XA(T) plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.824

cgatgaccggcgccatctcggcagccctggccgg-	CRISPR spacer
cgatgaccggttccatctcggcagcgc-gctcggt	Protospacer
**********. ************* * * .***

38. spacer 14.111|8791727|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.812

cgcacgtgggg-ggctgtcctcggtcagcaggg	CRISPR spacer
-gtagctggggaggttgtcctcggtcagcaggt	Protospacer
 *.*  ***** **.*****************

39. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_013860 (Azospirillum sp. B510 plasmid pAB510f, complete sequence) position: , mismatch: 6, identity: 0.829

-cgcgcgggccgcttcgaggtggtgcgcaagggcgt	CRISPR spacer
ctgcgc-agccgcttcgaggtggcgcgcaagggact	Protospacer
 .**** .***************.*********  *

40. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 6, identity: 0.829

-cgcgcgggccgcttcgaggtggtgcgcaagggcgt	CRISPR spacer
ctgcgc-agccgcttcgaggtggcgcgcaaggggct	Protospacer
 .**** .***************.*********  *

41. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029835 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence) position: , mismatch: 6, identity: 0.829

-cgcgcgggccgcttcgaggtggtgcgcaagggcgt	CRISPR spacer
ctgcgc-agccgcttcgaagtggcgcgcaagggcct	Protospacer
 .**** .**********.****.********** *

42. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to MH617110 (Microviridae sp. isolate ctdb208, complete genome) position: , mismatch: 7, identity: 0.788

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tttcctgctgcggccgcggccgcctctgcgata	Protospacer
.* .**********.***** **********.

43. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to NZ_CP015733 (Arthrobacter sp. U41 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.788

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tcgtctgctgcggctgcggcggccccggccgct	Protospacer
...*********************.* ** .**

44. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 7, identity: 0.811

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
ccgaggtggcggagcaggatttcgcccgggcgctgga	Protospacer
*. * *.**.***************** ********

45. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to MT711975 (Streptomyces phage Alderaan, complete genome) position: , mismatch: 7, identity: 0.781

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
gcgctgctgcggctgctccggcctctgctcct	Protospacer
   *************  **********  **

46. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 7, identity: 0.806

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cgaggtggcggagcaggatttcgcccgggcgctgga	Protospacer
. * *.**.***************** ********

47. spacer 14.38|8786555|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 7, identity: 0.788

gatggcttcccgtgcgccggccagcgcaatgcg	CRISPR spacer
cagcgcggcccgttcgccggccagcgcgatgcg	Protospacer
 *  **  ***** *************.*****

48. spacer 14.38|8786555|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 7, identity: 0.788

gatggcttcccgtgcgccggccagcgcaatgcg	CRISPR spacer
cagcgcggcccgttcgccggccagcgcgatgcg	Protospacer
 *  **  ***** *************.*****

49. spacer 14.38|8786555|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016463 (Bosea sp. RAC05 plasmid pBSY19_1, complete sequence) position: , mismatch: 7, identity: 0.788

gatggcttcccgtgcgccggccagcgcaatgcg	CRISPR spacer
gaatgcttcccgggcgccggccagagcagctcg	Protospacer
**  ******** *********** ***.. **

50. spacer 14.50|8787412|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.781

ttccacagtccgactagcgggccgcctgcgcg	CRISPR spacer
tgcggccggccgactcgcgggccgcctccgcg	Protospacer
* * .* * ****** *********** ****

51. spacer 14.53|8787624|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.788

-gccatcaccgagcagcgtcaactggttgcgcag	CRISPR spacer
caccat-gccgaacagcgtcaactggttgagcgt	Protospacer
 .**** .****.**************** **.

52. spacer 14.53|8787624|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

-gccatcaccgagcagcgtcaactggttgcgcag	CRISPR spacer
caccat-gccgaacagcgtcaactggttgagcgt	Protospacer
 .**** .****.**************** **.

53. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH001457 (Streptomyces phage Nesbitt, complete genome) position: , mismatch: 7, identity: 0.8

cgcgagggccttgagggcgctggtgatggcggtga-	CRISPR spacer
caggagggccttgagggcgtgggtgat-gcgctggt	Protospacer
*. ****************. ****** *** **.

54. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KT221033 (Streptomyces phage SF1, complete genome) position: , mismatch: 7, identity: 0.8

cgcgagggccttgagggcgctggtgatggcggtga-	CRISPR spacer
caggagggccttgagggcgtgggtgat-gcgctggt	Protospacer
*. ****************. ****** *** **.

55. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG593800 (Streptomyces phage AbbeyMikolon, complete genome) position: , mismatch: 7, identity: 0.8

cgcgagggccttgagggcgctggtgatggcggtga-	CRISPR spacer
caggagggccttgagggcgtgggtgat-gcgctggt	Protospacer
*. ****************. ****** *** **.

56. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022369 (Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence) position: , mismatch: 7, identity: 0.774

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgcggtcttc	Protospacer
*****************.* ****   ..**

57. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 7, identity: 0.774

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgcggtcttc	Protospacer
*****************.* ****   ..**

58. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.774

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgcggtcttc	Protospacer
*****************.* ****   ..**

59. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.774

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgcggtcttc	Protospacer
*****************.* ****   ..**

60. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.774

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccccgagctgtcgaagtagagcgcggtcttc	Protospacer
*****************.* ****   ..**

61. spacer 14.70|8788818|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to CP000876 (Herpetosiphon aurantiacus DSM 785 plasmid pHAU01, complete sequence) position: , mismatch: 7, identity: 0.788

tgctgcctctttcgcggcctgtgcttcggctgc	CRISPR spacer
tgcggcctgtttcgcggcctgtgctgccgaaga	Protospacer
*** **** **************** * *  *

62. spacer 14.70|8788818|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN694437 (Marine virus AFVG_250M820, complete genome) position: , mismatch: 7, identity: 0.788

tgctgcctctttcgcggcctgtgcttcggctgc	CRISPR spacer
tcctgcctctttcgctgcctgtgtttctttttc	Protospacer
* ************* *******.***  .* *

63. spacer 14.101|8791015|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK937607 (Gordonia phage Zipp, complete genome) position: , mismatch: 7, identity: 0.788

-gcagccggcccctggcggcgctctgtgcgtcgg	CRISPR spacer
caccgtc-gcccctggccgtgctctgtgcgtcga	Protospacer
 .* *.* ********* *.*************.

64. spacer 14.101|8791015|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to AP014693 (Ralstonia phage RSL2 DNA, complete sequence) position: , mismatch: 7, identity: 0.788

gcagccggcccctggcggcgctctgtgcgtcgg-	CRISPR spacer
acagccggtctctggcggcgctctg-gcgatgac	Protospacer
.*******.*.************** *** .*.

65. spacer 14.116|8792076|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048282 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence) position: , mismatch: 7, identity: 0.781

ttctcgcgggcacgctcgggtgcgccacgctc	CRISPR spacer
tcgacgcgggcacgatcgggtgcgccagtttc	Protospacer
*.  ********** ************  .**

66. spacer 14.118|8792216|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_008712 (Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence) position: , mismatch: 7, identity: 0.781

caccggaaggaccggcccacgaagacgctgga	CRISPR spacer
atggggaaggaccggcccacgaagaccctgcc	Protospacer
    ********************** ***

67. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 7, identity: 0.8

cgcgcgggccgcttcgaggtggtgcgcaagggcgt---	CRISPR spacer
cgcgcgggccgcttcgaggctgtgctc---ggcgctca	Protospacer
*******************. **** *   ****.

68. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 8, identity: 0.758

-acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
caaagc-cgcaccacggtgctgcgcgccgaggcg	Protospacer
 * .**  ********* ***** ********.

69. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

-acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
caaagc-cgcaccacggtgctgcgcgccgaggcg	Protospacer
 * .**  ********* ***** ********.

70. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

-acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
caaagc-cgcaccacggtgctgcgcgccgaggcg	Protospacer
 * .**  ********* ***** ********.

71. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_CP010860 (Marinovum algicola DG 898 plasmid pMaD5, complete sequence) position: , mismatch: 8, identity: 0.758

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
gcggcgggcgccacggggctgcccgaagggctg	Protospacer
.********.******.********  *.* *

72. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to MT711975 (Streptomyces phage Alderaan, complete genome) position: , mismatch: 8, identity: 0.758

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ggcgctgctgcggctgctccggcctctgctcct	Protospacer
    *************  **********  **

73. spacer 14.4|8785199|35|NZ_CP017169|PILER-CR matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 8, identity: 0.771

cgagttcgaggcactgcacgacaccttgctgcgca-	CRISPR spacer
cgagttcgagacactgctcgacaccgc-ccacgcgg	Protospacer
**********.****** ******* . *..***.

74. spacer 14.4|8785199|35|NZ_CP017169|PILER-CR matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 8, identity: 0.771

cgagttcgaggcactgcacgacaccttgctgcgca-	CRISPR spacer
cgagttcgagacactgctcgacaccgc-ccacgcgg	Protospacer
**********.****** ******* . *..***.

75. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

76. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
ccgaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*. * *. *.***************** ********

77. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

78. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

79. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

80. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

81. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

82. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

83. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

84. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

85. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

86. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

87. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

88. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

89. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

90. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

91. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

92. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

93. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

94. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

95. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

96. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

97. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

98. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

99. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

100. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

101. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

102. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

103. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

104. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

105. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

106. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

107. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

108. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

109. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

110. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

111. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

112. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

113. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

114. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

115. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

116. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

117. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

118. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

119. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

120. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

121. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

122. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.784

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cagaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
*  * *. *.***************** ********

123. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tcgctgctgctgctgcggcggcctcggccgtc	Protospacer
*  ******* ************** ** ...

124. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tcgctgctgctgctgcggcggcctcggccgtc	Protospacer
*  ******* ************** ** ...

125. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP033202 (Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ctgcgactgcggctgcggctgccactgcgaca	Protospacer
.  * .************* *** *******

126. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP003988 (Streptomyces sp. 769 plasmid pSGZL, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
gctgggctgctgctgcggcggcctccgcggcc	Protospacer
  *  ***** **************.***.*.

127. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to KY471269 (Gordonia phage DinoDaryn, complete genome) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ggaccgctgcggctgcggcgggttctgcgccc	Protospacer
 . *.**************** .****** *.

128. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to KY471268 (Gordonia phage Huffy, complete genome) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ggaccgctgcggctgcggcgggttctgcgccc	Protospacer
 . *.**************** .****** *.

129. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP013369 (Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact-	CRISPR spacer
acgatgatgcggctgcgtcggcctctg-gattg	Protospacer
    ** ********** ********* **.*

130. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP010607 (Phaeobacter inhibens strain P83 plasmid pP83_h, complete sequence) position: , mismatch: 8, identity: 0.75

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tccgtcctgcggctgcgacggcctcagcgtcg	Protospacer
* . * ***********.******* *** *

131. spacer 14.18|8785130|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 8, identity: 0.758

--gttccaccaggcggcaaccttcaccgtggtccg	CRISPR spacer
aaatgcaa--agggggcaatcttcaccgtggtcct	Protospacer
  .* * *  *** *****.**************

132. spacer 14.19|8785200|34|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 8, identity: 0.765

gagttcgaggcactgcacgacaccttgctgcgca-	CRISPR spacer
gagttcgagacactgctcgacaccgc-ccacgcgg	Protospacer
*********.****** ******* . *..***.

133. spacer 14.19|8785200|34|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 8, identity: 0.765

gagttcgaggcactgcacgacaccttgctgcgca-	CRISPR spacer
gagttcgagacactgctcgacaccgc-ccacgcgg	Protospacer
*********.****** ******* . *..***.

134. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
cgaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
. * *. *.***************** ********

135. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

136. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

137. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

138. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

139. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

140. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

141. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

142. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

143. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

144. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

145. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

146. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

147. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

148. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

149. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

150. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

151. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

152. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

153. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

154. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

155. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

156. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

157. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

158. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

159. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

160. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

161. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

162. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

163. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

164. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

165. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

166. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

167. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

168. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

169. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

170. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

171. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

172. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

173. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

174. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

175. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

176. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

177. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

178. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

179. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

180. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

181. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 8, identity: 0.778

ttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
agaggtcgcggagcaggatttcgcccgggcgctgga	Protospacer
  * *. *.***************** ********

182. spacer 14.33|8786200|34|NZ_CP017169|CRISPRCasFinder,CRT matches to MN961670 (Pseudomonas putida strain 420352 plasmid p420352-IMP, complete sequence) position: , mismatch: 8, identity: 0.765

gctgggctgacgtccagtcctgcctgctggcgga	CRISPR spacer
catcgggcgacggccagtcctgcttgctggcggg	Protospacer
  * ** .**** **********.*********.

183. spacer 14.63|8788333|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

gacacctggagctgccccacgccgaggtcacg	CRISPR spacer
tccgcctggaggtgccgcacgccgaggtgatc	Protospacer
  *.******* **** *********** *.

184. spacer 14.63|8788333|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH744418 (Streptomyces phage JustBecause, complete genome) position: , mismatch: 8, identity: 0.75

gacacctggagctgccccacgccgaggtcacg	CRISPR spacer
tgccgcgcgagctgcgccaccccgaggtcacg	Protospacer
 .*  *  ******* **** ***********

185. spacer 14.63|8788333|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MT310898 (Streptomyces phage Kela, complete genome) position: , mismatch: 8, identity: 0.75

gacacctggagctgccccacgccgaggtcacg	CRISPR spacer
tgccgcgcgagctgcgccaccccgaggtcacg	Protospacer
 .*  *  ******* **** ***********

186. spacer 14.64|8788402|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020399 (Burkholderia multivorans strain FDAARGOS_246 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.742

ccccgagctgtcgaagtggcgcgcctatctc	CRISPR spacer
ccggctcgtgccgaagtggcgcgcctatttc	Protospacer
**      **.*****************.**

187. spacer 14.65|8788470|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007515 (Rubrobacter radiotolerans strain RSPS-4 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.758

caccgcccaccgcatcaccacgtcccactggga	CRISPR spacer
ggccacgagccgcagcacctcgtcccactggga	Protospacer
 .**.*  .***** **** *************

188. spacer 14.65|8788470|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007517 (Rubrobacter radiotolerans strain RSPS-4 plasmid 3, complete sequence) position: , mismatch: 8, identity: 0.758

caccgcccaccgcatcaccacgtcccactggga	CRISPR spacer
ggccacgagccgcagcacctcgtcccactggga	Protospacer
 .**.*  .***** **** *************

189. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.75

atcaagctcgaagacaagccgccg----tgcccaaa	CRISPR spacer
ttcaagcccgaagaccagccgccgatgatccc----	Protospacer
 ******.******* ********    * **

190. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

atcaagctcgaagacaagccgccg----tgcccaaa	CRISPR spacer
ttcaagcccgaagaccagccgccgatgatccc----	Protospacer
 ******.******* ********    * **

191. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.765

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggttcgtccacgtgccgggcgaa	Protospacer
 *.*.  **************** *******.*

192. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 8, identity: 0.765

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggttcgtccacgtgccgggcgaa	Protospacer
 *.*.  **************** *******.*

193. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.765

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggttcgtccacgtgccgggcgaa	Protospacer
 *.*.  **************** *******.*

194. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.765

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggttcgtccacgtgccgggcgaa	Protospacer
 *.*.  **************** *******.*

195. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.765

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggttcgtccacgtgccgggcgaa	Protospacer
 *.*.  **************** *******.*

196. spacer 14.81|8789591|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP038140 (Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence) position: , mismatch: 8, identity: 0.765

gagtggcggccagcacccaccccatcatccaggc	CRISPR spacer
aaacgatgcccagcacccaccccatgatccgggc	Protospacer
.*..*..* **************** ****.***

197. spacer 14.81|8789591|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP038140 (Escherichia coli strain G3X16-2 plasmid pG3X16-2-3, complete sequence) position: , mismatch: 8, identity: 0.765

gagtggcggccagcacccaccccatcatccaggc	CRISPR spacer
aaacgatgcccagcacccaccccatgatccgggc	Protospacer
.*..*..* **************** ****.***

198. spacer 14.88|8790092|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024582 (Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ctgggactggtggggcccggtgcggatgtccc---	CRISPR spacer
ctgggaatggcggggcccggtgc---ttcaccggc	Protospacer
****** ***.************   * . **

199. spacer 14.88|8790092|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 8, identity: 0.75

ctgggactggtggggcccggtgcggatgtccc---	CRISPR spacer
ctgggaatggcggggcccggtgc---ttcaccggc	Protospacer
****** ***.************   * . **

200. spacer 14.89|8790161|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP034394 (Herbaspirillum seropedicae strain AU13965 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

gcaccacccgacccttgtcgcgagcctgcttca	CRISPR spacer
aaccgacccgccccttgtcgcgcgcctgcgcca	Protospacer
.  * ***** *********** ****** .**

201. spacer 14.92|8790374|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR134447 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 5, complete sequence) position: , mismatch: 8, identity: 0.765

tcgtcctcggctggcgtgtccgcggcatcgacgc--	CRISPR spacer
acgtccgcggcgggcgtgtccgcgg--gcagcgcgg	Protospacer
 ***** **** *************   *..***

202. spacer 14.110|8791656|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG812496 (Gordonia phage SallySpecial, complete genome) position: , mismatch: 8, identity: 0.765

cgatgaccggcgccatctcggcagccctggccgg	CRISPR spacer
ggatcaccggcgccatctcggcggccatcgggtg	Protospacer
 *** *****************.*** * *   *

203. spacer 14.116|8792076|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019037 (Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

ttctcgcgggcacgctcgggtgcgccacgctc	CRISPR spacer
cgctggtcggcacgctcgtgtgcgccccgctg	Protospacer
. ** *. ********** ******* ****

204. spacer 14.119|8792285|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 8, identity: 0.742

cggaacgtgaactgggcgggcagctccgcga	CRISPR spacer
aagcgcgtgaaatgggcggtcagctccgcat	Protospacer
 .* .****** ******* *********.

205. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_019339 (Arthrobacter sp. J3-49 plasmid pJ349-116, complete sequence) position: , mismatch: 8, identity: 0.771

cgcgcgggccgcttcgaggtggtgcgcaagggcgt	CRISPR spacer
ctcgcgggcggcttcgaggtggtccgcgacgcggg	Protospacer
* ******* ************* ***.* *  *

206. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
gcggcgggcaccaccgcgctgcccggatgcgcc	Protospacer
.************* * ********   . *.*

207. spacer 8.3|3469888|30|NZ_CP017169|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 9, identity: 0.7

gatgggcgggcaggctcctgcgacggctgg	CRISPR spacer
ccgccccgggcagggtccggcgacggctgt	Protospacer
      ******** *** **********

208. spacer 8.3|3469888|30|NZ_CP017169|CRT matches to NZ_CP021083 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence) position: , mismatch: 9, identity: 0.7

gatgggcgggcaggctcctgcgacggctgg	CRISPR spacer
cgcgggcgggcgggttcctgcgacggacca	Protospacer
 ..********.**.*********** . .

209. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ttcgctgctgctgctgcggcggcctcggccgtc	Protospacer
.*  ******* ************** ** ...

210. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to NZ_CP033202 (Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
actgcgactgcggctgcggctgccactgcgaca	Protospacer
 .  * .************* *** *******

211. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ttcgctgctgctgctgcggcggcctcggccgtc	Protospacer
.*  ******* ************** ** ...

212. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to NZ_CP003988 (Streptomyces sp. 769 plasmid pSGZL, complete sequence) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tgctgggctgctgctgcggcggcctccgcggcc	Protospacer
.  *  ***** **************.***.*.

213. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to KY471269 (Gordonia phage DinoDaryn, complete genome) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
aggaccgctgcggctgcggcgggttctgcgccc	Protospacer
  . *.**************** .****** *.

214. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to KY471268 (Gordonia phage Huffy, complete genome) position: , mismatch: 9, identity: 0.727

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
aggaccgctgcggctgcggcgggttctgcgccc	Protospacer
  . *.**************** .****** *.

215. spacer 14.3|8785129|34|NZ_CP017169|PILER-CR matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 9, identity: 0.735

--cgttccaccaggcggcaaccttcaccgtggtccg	CRISPR spacer
aaaatgcaa--agggggcaatcttcaccgtggtcct	Protospacer
   .* * *  *** *****.**************

216. spacer 14.9|8785554|34|NZ_CP017169|PILER-CR matches to NZ_CP049359 (Deinococcus wulumuqiensis R12 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.735

ctcgccgcgcctgggtgtcgttccgcccctggta	CRISPR spacer
cccggcgcgcctgggtgtcgtaccgcgcgagcac	Protospacer
*.** **************** **** *  *

217. spacer 14.9|8785554|34|NZ_CP017169|PILER-CR matches to NZ_CP031160 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence) position: , mismatch: 9, identity: 0.735

ctcgccgcgcctgggtgtcgttccgcccctggta	CRISPR spacer
cccggcgcgcctgggtgtcgtaccgcgcgagcac	Protospacer
*.** **************** **** *  *

218. spacer 14.13|8785841|36|NZ_CP017169|PILER-CR matches to MK388689 (Pantoea phage vB_PagM_LIET2, complete genome) position: , mismatch: 9, identity: 0.75

caccgcgt-acctggactgggtggaggagcaggccga	CRISPR spacer
-attaaatcatctggactggctggaagagcaggccga	Protospacer
 *... .* *.********* ****.***********

219. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP007648 (Lactobacillus salivarius strain JCM1046 plasmid pMP1046B, complete sequence) position: , mismatch: 9, identity: 0.719

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
ttgtcgctgcagctgcggctgcctctgcacca	Protospacer
*  ..*****.******** ********. *

220. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP023509 (Rothia mucilaginosa strain FDAARGOS_369 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tttctgctgcggctgcggctggctcattcggt	Protospacer
* ***************** * ***  . . *

221. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 9, identity: 0.719

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
cccccggtgcggcggcggcggcctcggcgagg	Protospacer
. .*.* ****** *********** ****

222. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP025513 (Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tgcgcgcttcggctgcggcggcctcggcctca	Protospacer
*.. .*** **************** **  *

223. spacer 14.22|8785412|36|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 9, identity: 0.75

ttacg-cggtggagcaggatttcgccccggcgctggc	CRISPR spacer
-cacaccggtggagcaggatttcgcccggtcgaacgg	Protospacer
 .**. ********************* * **   *

224. spacer 14.24|8785555|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP031160 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence) position: , mismatch: 9, identity: 0.727

tcgccgcgcctgggtgtcgttccgcccctggta	CRISPR spacer
ccggcgcgcctgggtgtcgtaccgcgcgagcac	Protospacer
.** **************** **** *  *

225. spacer 14.24|8785555|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP049359 (Deinococcus wulumuqiensis R12 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.727

tcgccgcgcctgggtgtcgttccgcccctggta	CRISPR spacer
ccggcgcgcctgggtgtcgtaccgcgcgagcac	Protospacer
.** **************** **** *  *

226. spacer 14.34|8786271|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP016024 (Ralstonia insidiosa strain ATCC 49129 plasmid pRI-1, complete sequence) position: , mismatch: 9, identity: 0.719

cgagcttccccgcagtcccaggagcaccccat	CRISPR spacer
tgagcttccccgcattgccaggagtagacatc	Protospacer
.************* * *******.*  *  .

227. spacer 14.49|8787342|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_008308 (Sphingomonas sp. KA1 plasmid pCAR3 DNA, complete sequence) position: , mismatch: 9, identity: 0.727

tgccccgggcattgttcgcatcgaggtgaaggg	CRISPR spacer
ggacccgggcatggatcgcatcgaggtaatcct	Protospacer
 * ********* * ************.*

228. spacer 14.51|8787481|34|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 9, identity: 0.735

cgcgccccggcgctggccgtccgaagggcagccg	CRISPR spacer
cgcgcccccgccctggccgtccgacacgtcgacc	Protospacer
******** ** ************ . *. * *

229. spacer 14.63|8788333|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 9, identity: 0.719

gacacctggagctgccccacgccgaggtcacg	CRISPR spacer
tccggctggaggtgccgcacgccgaggtgatc	Protospacer
  *. ****** **** *********** *.

230. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KU985096 (Mycobacterium phage Kazan, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

231. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG099952 (Mycobacterium phage WunderPhul, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

232. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK359352 (Mycobacterium phage JewelBug, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

233. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KX375815 (Mycobacterium phage ToneTone, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

234. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK494090 (Mycobacterium phage Jordennis, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

235. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KX641261 (Mycobacterium phage Isiphiwo, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

236. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KF560333 (Mycobacterium phage Artemis2UCLA, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

237. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KU695582 (Mycobacterium phage McFly, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

238. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MT024861 (Mycobacterium phage Pmask, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

239. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH155876 (Mycobacterium phage Priamo, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

240. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK359360 (Mycobacterium phage Hexamo, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

241. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH051253 (Mycobacterium phage GreedyLawyer, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

242. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MT657338 (Mycobacterium phage SuperCallie99, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

243. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_042334 (Mycobacterium virus Jeffabunny, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

244. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN728683 (Mycobacterium phage Yokurt, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

245. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_022965 (Mycobacterium phage CloudWang3, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

246. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to JF937092 (Mycobacterium phage DaVinci, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

247. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MF668288 (Mycobacterium phage Wiks, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

248. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH020240 (Mycobacterium phage SuperAwesome, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

249. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG099945 (Mycobacterium phage Koko, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

250. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK894433 (Mycobacterium phage Kipper29, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

251. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_022985 (Mycobacterium phage Zaka, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

252. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to JN049605 (Mycobacterium virus EricB, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

253. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN586039 (Mycobacterium phage Blinn1, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

254. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH779517 (Mycobacterium phage Zulu, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

255. spacer 14.73|8789027|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_029077 (Mycobacterium phage VohminGhazi, complete genome) position: , mismatch: 9, identity: 0.719

atcaagctcgaagacaagccgccgtgcccaaa	CRISPR spacer
ctgcagctcgaagaaaagccgccctgccgggt	Protospacer
 *  ********** ******** **** ..

256. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023017 (Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggtccgtccacgtgccgggcgaa	Protospacer
 *.*.  *******.******** *******.*

257. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggtccgtccacgtgccgggcgaa	Protospacer
 *.*.  *******.******** *******.*

258. spacer 14.76|8789236|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

ggtgaaggtgcggttcgtccacgagccgggcaac	CRISPR spacer
cgcggccgtgcggtccgtccacgtgccgggcgaa	Protospacer
 *.*.  *******.******** *******.*

259. spacer 14.83|8789732|36|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022666 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence) position: , mismatch: 9, identity: 0.75

ctactcgcgctcgtcctcgcccggcatcggcgtcag	CRISPR spacer
tgaccacccatcgttctcgtccggcatcggcgtcag	Protospacer
. **.  *  ****.****.****************

260. spacer 14.83|8789732|36|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050086 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence) position: , mismatch: 9, identity: 0.75

ctactcgcgctcgtcctcgcccggcatcggcgtcag	CRISPR spacer
tgaccacccatcgttctcgtccggcatcggcgtcag	Protospacer
. **.  *  ****.****.****************

261. spacer 14.88|8790092|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_017966 (Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence) position: , mismatch: 9, identity: 0.719

ctgggactggtggggcccggtgcggatgtccc------	CRISPR spacer
gtggaactggcggggcccggtgcg------ccgccgga	Protospacer
 ***.*****.*************      **

262. spacer 14.95|8790589|36|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009405 (Mycobacterium avium subsp. hominissuis strain OCU464 plasmid p78K, complete sequence) position: , mismatch: 9, identity: 0.75

aaggagtcg--gaggtcgccacggtgttcggcgccgtg	CRISPR spacer
--gtgaccggcgaggtcgccacggtggtcggcggcgtc	Protospacer
  * ...**  *************** ****** ***

263. spacer 14.111|8791727|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_023283 (Streptomyces sp. FR1 plasmid pFRL3, complete sequence) position: , mismatch: 9, identity: 0.719

cgcacgtggggggctgtcctcggtcagcaggg	CRISPR spacer
ctcggcaagggggcggtcctcggacagcaggc	Protospacer
* *.   .****** ******** *******

264. spacer 14.119|8792285|31|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_047866 (Aeromonas phage Ahp1, complete genome) position: , mismatch: 9, identity: 0.71

cggaacgtgaactgggcgggcagctccgcga	CRISPR spacer
ttcggtgtgaactgggcggccagctcggcta	Protospacer
.  ...************* ****** ** *

265. spacer 14.120|8792353|33|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026221 (Aeromonas sp. ASNIH4 plasmid pAER-f909, complete sequence) position: , mismatch: 9, identity: 0.727

acgcgccaggcccgcgaaggtccgca-----ctgcggg	CRISPR spacer
cggcgccaggaccgcggaggtccgcagccacct-----	Protospacer
  ******** *****.*********     **

266. spacer 14.128|8792924|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032678 (Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence) position: , mismatch: 9, identity: 0.743

cgcgcgggccgcttcgaggtggtgcgcaagggcgt	CRISPR spacer
ctatcgcatggcttcgaggtggggcgcaaaggcgt	Protospacer
*   ** .. ************ ******.*****

267. spacer 14.129|8792996|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG710528 (Escherichia phage GER2, complete genome) position: , mismatch: 9, identity: 0.743

tacgaggcgatggaacagcccgccttcgtgcggca	CRISPR spacer
gctgatccgatggaacagcccgcgttcatgcgtga	Protospacer
  .**  **************** ***.****  *

268. spacer 14.129|8792996|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_008464 (Stx2-converting phage 86, complete genome) position: , mismatch: 9, identity: 0.743

tacgaggcgatggaacagcccgccttcgtgcggca	CRISPR spacer
gctgatccgatggaacagcccgcgttcatgcgtga	Protospacer
  .**  **************** ***.****  *

269. spacer 14.129|8792996|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to AB255436 (Stx2-converting phage 86 DNA, complete genome) position: , mismatch: 9, identity: 0.743

tacgaggcgatggaacagcccgccttcgtgcggca	CRISPR spacer
gctgatccgatggaacagcccgcgttcatgcgtga	Protospacer
  .**  **************** ***.****  *

270. spacer 14.133|8793284|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_014819 (Asticcacaulis excentricus CB 48 plasmid pASTEX02, complete sequence) position: , mismatch: 9, identity: 0.719

ccgacgcctaaggctgaaggggagggtggtga	CRISPR spacer
gaagcgcctaaggccgaaggcgagggtgacgg	Protospacer
  ..**********.***** *******..*.

271. spacer 14.136|8793494|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017422 (Arthrobacter sp. ZXY-2 plasmid pZXY21, complete sequence) position: , mismatch: 9, identity: 0.735

acaagatctggccggtgaccctccgggctcttga---	CRISPR spacer
tgaacatctggacggtgaccctccgg---caggaaat	Protospacer
  ** ****** **************   *  **

272. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NC_006462 (Thermus thermophilus HB8 plasmid pTT27, complete sequence) position: , mismatch: 10, identity: 0.697

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
ctcctcggcaccacggacctccccgccgagccc	Protospacer
 .  . *********** ** ********* .*

273. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NC_017273 (Thermus thermophilus SG0.5JP17-16 plasmid pTHTHE1601, complete sequence) position: , mismatch: 10, identity: 0.697

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
ctcctcggcaccacggacctccccgccgagccc	Protospacer
 .  . *********** ** ********* .*

274. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_AP019802 (Thermus thermophilus strain HC11 plasmid pHC11, complete sequence) position: , mismatch: 10, identity: 0.697

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
ctcctcggcaccacggacctccccgccgagccc	Protospacer
 .  . *********** ** ********* .*

275. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NC_017588 (Thermus thermophilus JL-18 plasmid pTTJL1801, complete sequence) position: , mismatch: 10, identity: 0.697

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
ctcctcggcaccacggacctccccgccgagccc	Protospacer
 .  . *********** ** ********* .*

276. spacer 2.1|654742|33|NZ_CP017169|CRISPRCasFinder matches to NZ_LR027520 (Thermus thermophilus isolate TTHNAR1 plasmid 4, complete sequence) position: , mismatch: 10, identity: 0.697

acggcgggcaccacggagctgcccgccgaggtc	CRISPR spacer
ctcctcggcaccacggacctccccgccgagccc	Protospacer
 .  . *********** ** ********* .*

277. spacer 14.8|8785484|34|NZ_CP017169|PILER-CR matches to NZ_CP046573 (Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence) position: , mismatch: 10, identity: 0.706

cggtgcctggccccgctggcgttgagcctgtcga	CRISPR spacer
ctcatcctggccgcgctggggttgagcctgggtc	Protospacer
*    ******* ****** **********

278. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP032520 (Cupriavidus oxalaticus strain T2 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
cgcgcgctgcggctgcggtgtcctctgcgcgg	Protospacer
... .*************.* ********

279. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP040765 (Paracoccus sp. 2251 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
cggctgctgcggcggcggcgacctctctttcc	Protospacer
.. ********** ******.***** .  *.

280. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.688

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
catctgctgcgactgccgcggccttcaccttc	Protospacer
.**********.**** *******...*  ..

281. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
tgcgcgcggcggctgcggcggcctccgccggg	Protospacer
*.. .** *****************.** .

282. spacer 14.17|8785061|32|NZ_CP017169|CRISPRCasFinder,CRT matches to MK240575 (Thermobifida phage P318, complete genome) position: , mismatch: 10, identity: 0.688

tatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
cactggcttgggctgcggcggcctctgcttag	Protospacer
.*.. ***  ******************

283. spacer 14.20|8785271|32|NZ_CP017169|CRISPRCasFinder,CRT matches to NC_020548 (Azoarcus sp. KH32C plasmid pAZKH, complete sequence) position: , mismatch: 10, identity: 0.688

cccatcttgtagcgcttctccgtgggccgctt	CRISPR spacer
atgatcttgtagtgcttctctgtggggttttg	Protospacer
 . *********.*******.***** . .*

284. spacer 14.23|8785485|33|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP046573 (Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence) position: , mismatch: 10, identity: 0.697

ggtgcctggccccgctggcgttgagcctgtcga	CRISPR spacer
tcatcctggccgcgctggggttgagcctgggtc	Protospacer
    ******* ****** **********

285. spacer 14.28|8785842|35|NZ_CP017169|CRISPRCasFinder,CRT matches to MK388689 (Pantoea phage vB_PagM_LIET2, complete genome) position: , mismatch: 10, identity: 0.714

accgcgtacctggactgggtggaggagcaggccga	CRISPR spacer
ttaaatcatctggactggctggaagagcaggccga	Protospacer
 . .  .*.********* ****.***********

286. spacer 14.42|8786844|34|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_CP039433 (Rhodococcus sp. SGAir0479 plasmid unnamed) position: , mismatch: 10, identity: 0.706

ctccagatgctgtctgacgtgttcgttgtggcct	CRISPR spacer
tcgctcgcgctgtctgtcgtgttcgttgtcgcca	Protospacer
.. *  ..******** ************ ***

287. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN284893 (Mycobacterium phage LilMcDreamy, complete genome) position: , mismatch: 10, identity: 0.714

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
cttggccttgttgcgggcgctggtgatcgcggtga	Protospacer
* .*.   . *** ************* *******

288. spacer 14.66|8788540|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014308 (Burkholderia sp. PAMC 26561 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tcgccggcctggttctcaggctcttgtcctga	CRISPR spacer
gccccggccttgttctccggctcttgcggctt	Protospacer
 * ******* ****** ********.  .

289. spacer 14.66|8788540|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014309 (Burkholderia sp. PAMC 26561 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.688

tcgccggcctggttctcaggctcttgtcctga	CRISPR spacer
gccccggccttgttctccggctcttgcggctt	Protospacer
 * ******* ****** ********.  .

290. spacer 14.81|8789591|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027025 (Streptomyces sp. WAC00288 plasmid p3, complete sequence) position: , mismatch: 10, identity: 0.706

gagtggcggccagcacccaccccatcatccaggc	CRISPR spacer
tgaccgcggcccgcacccaccgcatcatccggat	Protospacer
 ... ****** ********* ********.*..

291. spacer 14.81|8789591|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

gagtggcggccagcacccaccccatcatccaggc	CRISPR spacer
tgaccgcggcccgcacccaccgcatcatccggat	Protospacer
 ... ****** ********* ********.*..

292. spacer 14.130|8793068|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

accttcaccgggctgatcgcggacaacagcatcgt	CRISPR spacer
gtgattgccgggctgatcgcggacagcggcatggc	Protospacer
..  *..******************.*.**** *.

293. spacer 14.2|8785060|33|NZ_CP017169|PILER-CR matches to NZ_CP032520 (Cupriavidus oxalaticus strain T2 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.667

ctatctgctgcggctgcggcggcctctgcgact	CRISPR spacer
acgcgcgctgcggctgcggtgtcctctgcgcgg	Protospacer
 ... .*************.* ********

294. spacer 14.7|8785411|37|NZ_CP017169|PILER-CR matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 11, identity: 0.703

cttacgcggtggagcaggatttcgccccggcgctggc	CRISPR spacer
ccacaccggtggagcaggatttcgcccggtcgaacgg	Protospacer
*.    ********************* * **   *

295. spacer 14.30|8785986|35|NZ_CP017169|CRISPRCasFinder,CRT matches to NZ_LR723671 (Rhizobium flavum strain YW14 plasmid 2) position: , mismatch: 11, identity: 0.686

ttgccctgcgtcttcttctcgatgccgcgccagtc	CRISPR spacer
cggatgtgcgtctggttctcgatgccgcgccccaa	Protospacer
. * . *******  ****************

296. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG812490 (Mycobacterium phage Holeinone, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

297. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH051249 (Mycobacterium phage Boyle, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

298. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN428049 (Mycobacterium phage West99, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

299. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN586045 (Mycobacterium phage Brownie5, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

300. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH001452 (Mycobacterium phage Kheth, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

301. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH697584 (Mycobacterium phage FrenchFry, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

302. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN813678 (Mycobacterium phage Lephleur, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

303. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG757162 (Mycobacterium phage Opia, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

304. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK814751 (Mycobacterium phage Bananafish, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

305. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KT365402 (Mycobacterium phage Tres, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

306. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KM101117 (Mycobacterium phage LizLemon, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

307. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to JN698991 (Mycobacterium phage Hedgerow, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

308. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NC_043767 (Mycobacterium virus TA17a, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

309. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN586046 (Mycobacterium phage Tinciduntsolum, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

310. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MT639652 (Mycobacterium phage MasterPo, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

311. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK620898 (Mycobacterium phage Coffee, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

312. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to JN699004 (Mycobacterium phage Ares, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

313. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MG812491 (Mycobacterium phage ItsyBitsy1, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

314. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MN234225 (Mycobacterium phage Rhinoforte, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

315. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to DQ398048 (Mycobacterium phage Qyrzula, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

316. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KR997932 (Mycobacterium phage Godines, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

317. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to AY129334 (Mycobacterium phage Rosebush, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

318. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH590591 (Mycobacterium phage Sabella, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

319. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to JN618996 (Mycobacterium phage Arbiter, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

320. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KX443696 (Mycobacterium phage Laurie, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

321. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MH727546 (Mycobacterium phage Eaglehorse, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

322. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to MK061411 (Mycobacterium phage Faze9, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

323. spacer 14.58|8787976|35|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to KT880194 (Mycobacterium phage Glass, complete genome) position: , mismatch: 11, identity: 0.686

cgcgagggccttgagggcgctggtgatggcggtga	CRISPR spacer
ctttttcttgttgcgcgcgctggtgatggcggtga	Protospacer
* .     . *** * *******************

324. spacer 14.66|8788540|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR027520 (Thermus thermophilus isolate TTHNAR1 plasmid 4, complete sequence) position: , mismatch: 11, identity: 0.656

tcgccggcctggttctcaggctcttgtcctga	CRISPR spacer
ggcccggcgtggttcccaggctcttgcgtccc	Protospacer
   ***** ******.**********. ..

325. spacer 14.92|8790374|34|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026189 (Enterobacteriaceae bacterium ENNIH2 plasmid pENT-812c, complete sequence) position: , mismatch: 11, identity: 0.676

tcgtcctcggctggcgtgtccgcggcatcgacgc	CRISPR spacer
aaaggatcggctggcgtgaccacggcatcggcag	Protospacer
  .   ************ **.********.*.

326. spacer 14.111|8791727|32|NZ_CP017169|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016082 (Streptomyces sp. SAT1 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.656

cgcacgtggggggctgtcctcggtcagcaggg	CRISPR spacer
gatgacccgggggccgtcctcggccagcagga	Protospacer
 ...  . ******.********.*******.

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

2035311 : 2115399

Shigella_phage(33.33%)

transposase,protease

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_140853429.1\|2035311_2036343_+\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140853430.1\|2037162_2038485_-	galactose oxidase	NA	NA	NA	NA
WP_140853431.1\|2038475_2039375_-	hypothetical protein	NA	NA	NA	NA
WP_140853429.1\|2039493_2040525_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140853493.1\|2040521_2041082_-\|transposase	transposase	NA	NA	NA	NA
WP_140853432.1\|2042295_2043189_-	RNA polymerase subunit sigma-70	NA	NA	NA	NA
WP_140853433.1\|2043185_2046332_-	tetratricopeptide repeat protein	L7RGQ5	Acanthamoeba_polyphaga_moumouvirus	3.9e-16	26.2
WP_140788921.1\|2048694_2049111_+	cupin domain-containing protein	NA	NA	NA	NA
WP_140853434.1\|2049146_2050046_+	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_140788924.1\|2050430_2050784_-	VOC family protein	NA	NA	NA	NA
WP_140853435.1\|2050953_2051823_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140797660.1\|2052006_2052606_+	hypothetical protein	NA	NA	NA	NA
WP_161606743.1\|2054795_2055848_-	hypothetical protein	NA	NA	NA	NA
WP_140788926.1\|2057281_2058046_-	hypothetical protein	NA	NA	NA	NA
WP_140853436.1\|2058209_2059091_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140858220.1\|2059239_2059899_+	ankyrin repeat domain-containing protein	NA	NA	NA	NA
WP_140788929.1\|2059898_2060360_+	nucleoside deaminase	NA	NA	NA	NA
WP_161606744.1\|2060819_2061371_+	TetR family transcriptional regulator	NA	NA	NA	NA
WP_161605135.1\|2063596_2063926_-	hypothetical protein	NA	NA	NA	NA
WP_161606745.1\|2064035_2066960_+	FG-GAP repeat protein	NA	NA	NA	NA
WP_140788932.1\|2067046_2067946_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140796383.1\|2068091_2069012_+	pyridoxal-phosphate dependent enzyme	NA	NA	NA	NA
WP_140788933.1\|2069484_2070513_+	hypothetical protein	NA	NA	NA	NA
WP_140788935.1\|2070777_2071125_+	hypothetical protein	NA	NA	NA	NA
WP_140788936.1\|2071398_2071662_-	hypothetical protein	NA	NA	NA	NA
WP_140788937.1\|2071658_2072195_-	hypothetical protein	NA	NA	NA	NA
WP_020479202.1\|2072230_2072518_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_140788938.1\|2072514_2073198_+	SdpI family protein	NA	NA	NA	NA
WP_140858222.1\|2073380_2074289_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_140853439.1\|2075470_2076298_-\|protease	protease	NA	NA	NA	NA
WP_174258697.1\|2077313_2080418_-	tetratricopeptide repeat protein	M1HTZ5	Acanthocystis_turfacea_Chlorella_virus	4.3e-07	28.3
WP_140853440.1\|2080843_2085673_+	DNA/RNA non-specific endonuclease	NA	NA	NA	NA
WP_161604861.1\|2085786_2085960_+	hypothetical protein	NA	NA	NA	NA
WP_161604862.1\|2086098_2086272_+	hypothetical protein	NA	NA	NA	NA
WP_140788943.1\|2086256_2086448_+	hypothetical protein	NA	NA	NA	NA
WP_140853441.1\|2087285_2087786_-\|transposase	transposase	NA	NA	NA	NA
WP_140788947.1\|2088103_2088607_-	hypothetical protein	NA	NA	NA	NA
WP_174258576.1\|2089794_2090040_+	hypothetical protein	NA	NA	NA	NA
WP_161604864.1\|2090551_2091847_-	serine hydrolase	A0A1V0SLG8	Klosneuvirus	1.4e-12	29.7
WP_140788949.1\|2093208_2093499_-	hypothetical protein	NA	NA	NA	NA
WP_140858226.1\|2094803_2097245_-	Ig-like domain-containing protein	NA	NA	NA	NA
WP_140853442.1\|2097951_2098959_-	hypothetical protein	NA	NA	NA	NA
WP_161606746.1\|2099709_2099925_-	hypothetical protein	NA	NA	NA	NA
WP_140788952.1\|2100573_2101497_+	hypothetical protein	NA	NA	NA	NA
WP_140853443.1\|2101705_2102419_+	hypothetical protein	NA	NA	NA	NA
WP_140796388.1\|2102638_2103217_-	pirin family protein	NA	NA	NA	NA
WP_140853444.1\|2103594_2104425_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140788956.1\|2105807_2106173_-	gas vesicle protein	NA	NA	NA	NA
WP_140853445.1\|2106207_2106534_-	gas vesicle protein K	NA	NA	NA	NA
WP_011552834.1\|2106582_2106804_-	gas vesicle protein	NA	NA	NA	NA
WP_140788959.1\|2106800_2107082_-	gas vesicle protein GvpG	NA	NA	NA	NA
WP_140788961.1\|2107078_2107888_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140788962.1\|2107918_2108143_-	gas vesicle structural protein GvpA	NA	NA	NA	NA
WP_140788963.1\|2108150_2108918_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140858228.1\|2108914_2109733_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140853446.1\|2109753_2111889_-	CDC48 family AAA ATPase	A0A2K9R7H3	Dishui_lake_phycodnavirus	3.4e-48	48.0
WP_140853447.1\|2111885_2112410_-	Hsp20/alpha crystallin family protein	NA	NA	NA	NA
WP_140853448.1\|2112751_2114026_+	PDZ domain-containing protein	NA	NA	NA	NA
WP_140853449.1\|2114397_2115399_+\|transposase	IS630 family transposase	NA	NA	NA	NA

DBSCAN-SWA_2

2120109 : 2176343

uncultured_virus(33.33%)

transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140858130.1\|2120109_2121075_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_140853451.1\|2121324_2121726_+\|transposase	transposase	NA	NA	NA	NA
WP_140797681.1\|2122740_2124165_-	DUF1552 domain-containing protein	NA	NA	NA	NA
WP_140800641.1\|2124161_2125685_-	DUF1592 domain-containing protein	NA	NA	NA	NA
WP_140853452.1\|2126116_2127487_-	hypothetical protein	NA	NA	NA	NA
WP_140797683.1\|2128527_2128755_+	hypothetical protein	NA	NA	NA	NA
WP_140795586.1\|2129463_2129778_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140795585.1\|2129743_2130148_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140795584.1\|2130194_2131715_+\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	4.9e-57	33.6
WP_140853453.1\|2131926_2132454_+\|transposase	transposase	NA	NA	NA	NA
WP_140788984.1\|2132851_2133160_+	hypothetical protein	NA	NA	NA	NA
WP_140788986.1\|2134229_2135447_+	HlyD family efflux transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_140788988.1\|2135449_2138179_+	ATP-binding cassette domain-containing protein	A0A076FI99	Aureococcus_anophage	7.3e-19	27.7
WP_140788990.1\|2138175_2140287_+	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	4.0e-09	29.1
WP_140853454.1\|2140283_2141783_+	TolC family protein	NA	NA	NA	NA
WP_140788994.1\|2141789_2143538_+	hypothetical protein	NA	NA	NA	NA
WP_140788996.1\|2143546_2144557_+	phosphotransferase	NA	NA	NA	NA
WP_140858233.1\|2145313_2145841_+\|transposase	transposase	NA	NA	NA	NA
WP_161606748.1\|2146322_2146487_-	hypothetical protein	NA	NA	NA	NA
WP_140853455.1\|2146718_2148239_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	2.9e-57	33.6
WP_140853456.1\|2148285_2148651_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140795586.1\|2148655_2148970_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140853457.1\|2149460_2151623_-	hypothetical protein	NA	NA	NA	NA
WP_140853458.1\|2152118_2153504_-	DUF2079 domain-containing protein	NA	NA	NA	NA
WP_140795586.1\|2153738_2154053_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140853456.1\|2154057_2154423_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140853455.1\|2154469_2155990_+\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	2.9e-57	33.6
WP_140853459.1\|2156083_2156272_+	hypothetical protein	NA	NA	NA	NA
WP_140853460.1\|2156519_2157557_-	DUF4062 domain-containing protein	NA	NA	NA	NA
WP_140796391.1\|2159478_2160006_+\|transposase	transposase	NA	NA	NA	NA
WP_140789000.1\|2160469_2161117_-	TetR/AcrR family transcriptional regulator C-terminal ligand-binding domain-containing protein	NA	NA	NA	NA
WP_140789002.1\|2161262_2161781_+	GNAT family N-acetyltransferase	A0A1P8CWJ6	Bacillus_phage	4.0e-11	33.3
WP_162521008.1\|2161933_2162239_-\|transposase	transposase	NA	NA	NA	NA
WP_161604868.1\|2162347_2162581_+	hypothetical protein	NA	NA	NA	NA
WP_140789005.1\|2162943_2163177_+	hypothetical protein	NA	NA	NA	NA
WP_140789007.1\|2163159_2163474_-	hypothetical protein	NA	NA	NA	NA
WP_140789009.1\|2164198_2164618_+	DUF1036 domain-containing protein	NA	NA	NA	NA
WP_140796392.1\|2164729_2164960_-	hypothetical protein	NA	NA	NA	NA
WP_140789011.1\|2164968_2165361_-	gamma-glutamylcyclotransferase	H9D1E0	Salinivibrio_phage	2.2e-09	39.0
WP_140796393.1\|2165357_2165801_-	gamma-glutamylcyclotransferase	NA	NA	NA	NA
WP_140853461.1\|2167207_2167549_-	hypothetical protein	NA	NA	NA	NA
WP_140853462.1\|2167669_2168827_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_140853463.1\|2169028_2170186_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_140789017.1\|2170446_2171445_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	7.8e-11	29.3
WP_140796394.1\|2171990_2172485_-	ankyrin repeat domain-containing protein	NA	NA	NA	NA
WP_161606749.1\|2174381_2175332_-	hypothetical protein	NA	NA	NA	NA
WP_140789021.1\|2175635_2176343_+\|transposase	IS5 family transposase	A0A0N9SHJ4	Paenibacillus_phage	1.1e-14	38.5

DBSCAN-SWA_3

2204158 : 2247125

uncultured_virus(25.0%)

portal,tail,plate,transposase,head,capsid

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140853486.1\|2204158_2205496_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140853487.1\|2205505_2205901_-	hypothetical protein	NA	NA	NA	NA
WP_140853488.1\|2205905_2206601_-	hypothetical protein	NA	NA	NA	NA
WP_140853489.1\|2206608_2207139_-	hypothetical protein	NA	NA	NA	NA
WP_174258699.1\|2207140_2208670_-\|plate	baseplate J/gp47 family protein	NA	NA	NA	NA
WP_140853491.1\|2208815_2209496_+	glycosyltransferase	NA	NA	NA	NA
WP_140853492.1\|2212188_2213598_+	hypothetical protein	A0A1P8D5S9	Corynebacterium_phage	6.2e-06	34.9
WP_140853493.1\|2214125_2214686_+\|transposase	transposase	NA	NA	NA	NA
WP_140853429.1\|2214682_2215714_+\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140858245.1\|2215676_2215973_-\|transposase	transposase	NA	NA	NA	NA
WP_140853494.1\|2216219_2216564_+	hypothetical protein	NA	NA	NA	NA
WP_140853495.1\|2217490_2217883_-	GPW/gp25 family protein	NA	NA	NA	NA
WP_140853496.1\|2217893_2218568_-	hypothetical protein	NA	NA	NA	NA
WP_140853497.1\|2218576_2219155_-	hypothetical protein	NA	NA	NA	NA
WP_140853498.1\|2219165_2220449_-	phage late control D family protein	NA	NA	NA	NA
WP_140853499.1\|2220445_2220787_-	hypothetical protein	NA	NA	NA	NA
WP_140853500.1\|2220786_2221299_-	peptidoglycan-binding protein	NA	NA	NA	NA
WP_140853501.1\|2221313_2224007_-\|tail	phage tail tape measure protein	A0A2H4J055	uncultured_Caudovirales_phage	4.4e-24	30.1
WP_140853503.1\|2224198_2224972_-	hypothetical protein	NA	NA	NA	NA
WP_140853504.1\|2225092_2225875_+	NYN domain-containing protein	NA	NA	NA	NA
WP_140853505.1\|2225878_2226340_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140853507.1\|2228565_2228895_-	hypothetical protein	NA	NA	NA	NA
WP_140853508.1\|2228891_2229791_-	IPT/TIG domain-containing protein	NA	NA	NA	NA
WP_140853509.1\|2229790_2230396_-	hypothetical protein	NA	NA	NA	NA
WP_140853510.1\|2230403_2231045_-	hypothetical protein	NA	NA	NA	NA
WP_174259044.1\|2231041_2231272_-	hypothetical protein	NA	NA	NA	NA
WP_140853512.1\|2231346_2231871_-	hypothetical protein	NA	NA	NA	NA
WP_140853513.1\|2231870_2232509_-	hypothetical protein	NA	NA	NA	NA
WP_140853514.1\|2232510_2232888_-	hypothetical protein	NA	NA	NA	NA
WP_140853515.1\|2233060_2233840_-\|capsid	phage major capsid protein	A0A1B1P7E3	Bacillus_phage	2.1e-35	42.9
WP_140853516.1\|2233885_2234563_-	hypothetical protein	NA	NA	NA	NA
WP_140853517.1\|2234559_2235912_-	DNA adenine methylase	A0A0H3UZK1	Geobacillus_virus	2.7e-22	28.3
WP_174258700.1\|2235904_2236078_-	hypothetical protein	NA	NA	NA	NA
WP_140853518.1\|2236132_2237212_-\|head	head morphogenesis protein	NA	NA	NA	NA
WP_140853519.1\|2237192_2237474_-	hypothetical protein	NA	NA	NA	NA
WP_140853520.1\|2237470_2239495_-\|portal	phage portal protein	A0A0U3E050	Pseudomonas_phage	1.2e-50	30.7
WP_140853521.1\|2239949_2241968_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_161606750.1\|2242104_2242299_-	hypothetical protein	NA	NA	NA	NA
WP_140795586.1\|2242460_2242775_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140853456.1\|2242779_2243145_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140795584.1\|2243400_2244921_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	4.9e-57	33.6
WP_140853456.1\|2244967_2245333_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140795586.1\|2245337_2245652_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140858250.1\|2245724_2247125_+\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	5.9e-57	33.6

DBSCAN-SWA_4

2401821 : 2412446

Bacillus_thuringiensis_phage(14.29%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140853579.1\|2401821_2404674_+	response regulator	Q56AR1	Bacillus_thuringiensis_phage	3.0e-07	31.3
WP_140853580.1\|2404723_2405719_+\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD	A0A0R6PI74	Moraxella_phage	5.8e-75	46.6
WP_140789208.1\|2405733_2406585_+	16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))- dimethyltransferase RsmA	E4ZFQ0	Streptococcus_phage	6.4e-14	33.7
WP_043710562.1\|2406592_2406871_-	hypothetical protein	NA	NA	NA	NA
WP_011552138.1\|2407081_2407726_+	deoxynucleoside kinase	A0A288TXV5	Enterococcus_phage	2.6e-15	32.8
WP_140789212.1\|2407890_2408808_+	3-methyl-2-oxobutanoate hydroxymethyltransferase	M4QNT1	Ostreococcus_lucimarinus_virus	9.5e-48	38.4
WP_140789214.1\|2408810_2409689_+	pantoate--beta-alanine ligase	NA	NA	NA	NA
WP_140789216.1\|2409685_2410174_+	SsrA-binding protein SmpB	W5RAM5	Staphylococcus_phage	2.1e-30	47.2
WP_140789218.1\|2410207_2410729_+	stringent starvation protein B	NA	NA	NA	NA
WP_140853581.1\|2410736_2412446_-	protein kinase	A0A0G2Y7N1	Acanthamoeba_polyphaga_mimivirus	7.8e-11	27.8

DBSCAN-SWA_5

3738556 : 3788919

Clostridium_phage(20.0%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140790875.1\|3738556_3739897_+\|protease	M6 family metalloprotease domain-containing protein	A0A1L2BY89	Clostridium_phage	2.6e-30	29.9
WP_140854436.1\|3740335_3741223_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140790879.1\|3741342_3741747_+	RidA family protein	NA	NA	NA	NA
WP_140854438.1\|3741918_3744243_-	ethanolamine ammonia-lyase subunit EutB	NA	NA	NA	NA
WP_002640507.1\|3744495_3745389_+	1,4-dihydroxy-2-naphthoyl-CoA synthase	NA	NA	NA	NA
WP_140798257.1\|3745480_3745885_+	hypothetical protein	NA	NA	NA	NA
WP_174258789.1\|3745901_3746576_-	hemolysin III family protein	NA	NA	NA	NA
WP_140798258.1\|3747008_3748007_+	hypothetical protein	NA	NA	NA	NA
WP_140854443.1\|3748154_3751466_+	hypothetical protein	NA	NA	NA	NA
WP_140854444.1\|3751622_3753734_+	peptidase M13	E3T4I7	Cafeteria_roenbergensis_virus	4.1e-86	31.3
WP_140790891.1\|3753787_3754012_+	hypothetical protein	NA	NA	NA	NA
WP_174258790.1\|3754036_3755674_-	fumarate hydratase	NA	NA	NA	NA
WP_140798261.1\|3755885_3757238_+	OmpA family protein	NA	NA	NA	NA
WP_140790896.1\|3757483_3758116_+	hypothetical protein	NA	NA	NA	NA
WP_140854445.1\|3758158_3759817_-	hypothetical protein	NA	NA	NA	NA
WP_026114162.1\|3760291_3761023_-	hypothetical protein	NA	NA	NA	NA
WP_140854447.1\|3761260_3761842_+	hypothetical protein	NA	NA	NA	NA
WP_140854449.1\|3761908_3762823_-	hypothetical protein	NA	NA	NA	NA
WP_140858326.1\|3762892_3764086_-	J domain-containing protein	NA	NA	NA	NA
WP_140858329.1\|3764205_3765009_-	hypothetical protein	NA	NA	NA	NA
WP_140790901.1\|3765213_3766158_+	DUF808 family protein	NA	NA	NA	NA
WP_140854451.1\|3766207_3767023_-	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_174258791.1\|3767019_3768048_-	NADP-dependent oxidoreductase	NA	NA	NA	NA
WP_140854455.1\|3768218_3769289_+\|protease	FtsH protease activity modulator HflK	NA	NA	NA	NA
WP_140790908.1\|3769285_3770224_+\|protease	protease modulator HflC	NA	NA	NA	NA
WP_162521005.1\|3770311_3770671_-	hypothetical protein	NA	NA	NA	NA
WP_140854457.1\|3770629_3770920_+	cytochrome P450	NA	NA	NA	NA
WP_140854459.1\|3770988_3772347_-	general secretion pathway protein GspE	NA	NA	NA	NA
WP_140790914.1\|3772426_3774049_-	hypothetical protein	NA	NA	NA	NA
WP_140790916.1\|3774561_3775485_+	endonuclease/exonuclease/phosphatase family protein	NA	NA	NA	NA
WP_140854461.1\|3775457_3776153_+	hypothetical protein	NA	NA	NA	NA
WP_140790920.1\|3776208_3776763_-	hypothetical protein	NA	NA	NA	NA
WP_140854463.1\|3777652_3778018_-	serine hydrolase	NA	NA	NA	NA
WP_140854465.1\|3778445_3779102_-	DUF664 domain-containing protein	NA	NA	NA	NA
WP_140854467.1\|3779393_3783104_-	ATP-dependent RNA helicase HrpA	A0A1V0SBU4	Catovirus	8.3e-42	27.1
WP_161605152.1\|3783151_3783487_+\|transposase	transposase	NA	NA	NA	NA
WP_161606764.1\|3783929_3784295_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_161606765.1\|3785952_3786621_+\|transposase	transposase	NA	NA	NA	NA
WP_140790937.1\|3786617_3786986_-	acyl carrier protein	K4FB26	Cronobacter_phage	8.9e-05	40.8
WP_140795584.1\|3787398_3788919_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	4.9e-57	33.6

DBSCAN-SWA_6

4200729 : 4224016

Burkholderia_virus(50.0%)

portal,tail,transposase,protease,head,terminase,capsid

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140854726.1\|4200729_4201116_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140854729.1\|4201154_4201583_-	hypothetical protein	NA	NA	NA	NA
WP_140854731.1\|4201594_4202044_-	hypothetical protein	NA	NA	NA	NA
WP_140854733.1\|4202064_4202469_-	hypothetical protein	NA	NA	NA	NA
WP_140854735.1\|4202465_4202786_-	hypothetical protein	NA	NA	NA	NA
WP_140854737.1\|4202785_4203433_-	hypothetical protein	NA	NA	NA	NA
WP_140854739.1\|4203445_4203880_-	hypothetical protein	NA	NA	NA	NA
WP_140854741.1\|4203946_4205119_-\|capsid	phage major capsid protein	A4JX01	Burkholderia_virus	3.2e-16	26.9
WP_140854743.1\|4205184_4206096_-\|head,protease	HK97 family phage prohead protease	NA	NA	NA	NA
WP_140858353.1\|4206114_4207431_-\|portal	phage portal protein	NA	NA	NA	NA
WP_140854746.1\|4209255_4210164_-	hypothetical protein	NA	NA	NA	NA
WP_140854748.1\|4210252_4211770_-\|terminase	large terminase	NA	NA	NA	NA
WP_140854750.1\|4211759_4212347_-	hypothetical protein	NA	NA	NA	NA
WP_161606772.1\|4212643_4212964_-	hypothetical protein	NA	NA	NA	NA
WP_140854752.1\|4213646_4214066_+	hypothetical protein	NA	NA	NA	NA
WP_140854755.1\|4214131_4214800_-	DUF3251 domain-containing protein	NA	NA	NA	NA
WP_140854757.1\|4214798_4215188_+	hypothetical protein	NA	NA	NA	NA
WP_140854759.1\|4215223_4215502_+	hypothetical protein	NA	NA	NA	NA
WP_140854761.1\|4215546_4216014_+	C40 family peptidase	NA	NA	NA	NA
WP_140854764.1\|4216067_4216607_+	hypothetical protein	NA	NA	NA	NA
WP_140854766.1\|4216609_4216822_+	hypothetical protein	NA	NA	NA	NA
WP_140854770.1\|4217794_4218013_-	hypothetical protein	NA	NA	NA	NA
WP_140854772.1\|4218035_4218380_-	hypothetical protein	NA	NA	NA	NA
WP_140858356.1\|4219185_4220166_+	hypothetical protein	NA	NA	NA	NA
WP_140854776.1\|4220460_4220652_-	questin oxidase family protein	NA	NA	NA	NA
WP_140854778.1\|4220648_4220858_-	hypothetical protein	NA	NA	NA	NA
WP_140854780.1\|4220854_4221181_-	hypothetical protein	NA	NA	NA	NA
WP_140854782.1\|4221251_4222409_-	hypothetical protein	NA	NA	NA	NA
WP_140795584.1\|4222495_4224016_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	4.9e-57	33.6

DBSCAN-SWA_7

5212275 : 5228979

Shigella_phage(40.0%)

transposase,integrase

attL 5212486:5212545|attR 5229001:5230698

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140858403.1\|5212275_5212683_-\|integrase	tyrosine-type recombinase/integrase	A0A2D2W4Z2	Ralstonia_phage	2.8e-07	46.7
5212486:5212545	attL	NA	NA	NA	NA
WP_140853493.1\|5212566_5213127_+\|transposase	transposase	NA	NA	NA	NA
WP_140853429.1\|5213123_5214155_+\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140855367.1\|5214184_5215198_-\|integrase	tyrosine-type recombinase/integrase	A0A2I7SC08	Paenibacillus_phage	4.9e-13	27.4
WP_140797768.1\|5215194_5215446_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140797769.1\|5215442_5216978_-	hypothetical protein	I6NPA6	Burkholderia_phage	1.4e-11	32.7
WP_140797770.1\|5216974_5218090_-	hypothetical protein	NA	NA	NA	NA
WP_002636263.1\|5218350_5218587_-	ArsR family transcriptional regulator	NA	NA	NA	NA
WP_161605141.1\|5219060_5219981_+	DUF2381 family protein	NA	NA	NA	NA
WP_140797772.1\|5219896_5221834_+	protein kinase	NA	NA	NA	NA
WP_140855370.1\|5222012_5223308_+	protein kinase	NA	NA	NA	NA
WP_140855372.1\|5223428_5224781_+	hypothetical protein	NA	NA	NA	NA
WP_140855374.1\|5224770_5226306_+	DUF2380 domain-containing protein	NA	NA	NA	NA
WP_140855376.1\|5226302_5226773_+	NUDIX hydrolase	NA	NA	NA	NA
WP_140853429.1\|5227390_5228422_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140853493.1\|5228418_5228979_-\|transposase	transposase	NA	NA	NA	NA
5229001:5230698	attR	NA	NA	NA	NA

DBSCAN-SWA_8

5663818 : 5712093

Klosneuvirus(16.67%)

tRNA,plate,tail

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140855635.1\|5663818_5667712_-\|tRNA	valine--tRNA ligase	A0A1V0SK04	Klosneuvirus	3.3e-158	40.8
WP_140793067.1\|5667776_5669042_-	response regulator	NA	NA	NA	NA
WP_140793068.1\|5669158_5669974_-	chemotaxis protein CheW	NA	NA	NA	NA
WP_140793070.1\|5670024_5671398_+	diguanylate cyclase	A0A127AWB9	Bacillus_phage	1.2e-17	33.5
WP_140793072.1\|5671401_5671794_-	demethoxyubiquinone hydroxylase family protein	NA	NA	NA	NA
WP_161606781.1\|5671943_5673461_+	hybrid histidine protein kinase/response regulator SinK	Q8QKV7	Ectocarpus_siliculosus_virus	9.4e-08	21.7
WP_140855640.1\|5673457_5674540_+	signal integration modulator SinM	NA	NA	NA	NA
WP_140793078.1\|5674717_5676361_-	chaperonin GroEL	A0A240F779	uncultured_virus	8.2e-167	58.2
WP_002639463.1\|5676529_5676886_-	response regulator	NA	NA	NA	NA
WP_174258867.1\|5676978_5678049_+	metallopeptidase family protein	NA	NA	NA	NA
WP_140855644.1\|5678002_5678980_-	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_140855646.1\|5679026_5679725_+	WHG domain-containing protein	NA	NA	NA	NA
WP_140855649.1\|5680081_5681371_-	hypothetical protein	NA	NA	NA	NA
WP_140855651.1\|5681367_5681865_-	HNH endonuclease	NA	NA	NA	NA
WP_140855653.1\|5682066_5682768_-	hypothetical protein	NA	NA	NA	NA
WP_140855656.1\|5685384_5686311_+	DUF2381 family protein	NA	NA	NA	NA
WP_140793159.1\|5687288_5687633_-	DUF1768 domain-containing protein	A0A141ZK81	Faustovirus	2.1e-08	46.0
WP_140796562.1\|5687547_5687985_-	hypothetical protein	NA	NA	NA	NA
WP_140855658.1\|5688781_5693878_+	DUF4157 domain-containing protein	NA	NA	NA	NA
WP_140855660.1\|5693881_5694631_+	hypothetical protein	NA	NA	NA	NA
WP_140855662.1\|5694627_5695638_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_140793168.1\|5695789_5696383_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_140855664.1\|5696379_5697111_+	hypothetical protein	NA	NA	NA	NA
WP_140855666.1\|5697155_5699540_+\|tail	phage tail sheath subtilisin-like domain-containing protein	H6WFT7	Cyanophage	2.7e-17	34.0
WP_011554491.1\|5699558_5700014_+\|tail	phage tail protein	NA	NA	NA	NA
WP_140855668.1\|5700042_5701614_+\|tail	phage tail sheath protein	NA	NA	NA	NA
WP_140793178.1\|5701610_5702090_+\|tail	phage tail protein	NA	NA	NA	NA
WP_140855671.1\|5702096_5703416_+	hypothetical protein	NA	NA	NA	NA
WP_174258868.1\|5703419_5703593_+	hypothetical protein	NA	NA	NA	NA
WP_140855673.1\|5703611_5704688_+	phage late control D family protein	NA	NA	NA	NA
WP_140855676.1\|5704684_5705383_+	hypothetical protein	NA	NA	NA	NA
WP_140855679.1\|5705313_5706921_+	hypothetical protein	NA	NA	NA	NA
WP_140793188.1\|5706928_5707330_+	GPW/gp25 family protein	NA	NA	NA	NA
WP_140855681.1\|5707330_5709673_+\|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_140855683.1\|5709672_5712093_+\|tail	phage tail protein	NA	NA	NA	NA

DBSCAN-SWA_9

7677227 : 7712143

Paramecium_bursaria_Chlorella_virus(66.67%)

bacteriocin,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140858556.1\|7677227_7677815_-\|bacteriocin	bacteriocin fulvocin C-related protein	NA	NA	NA	NA
WP_140858558.1\|7678693_7680028_-	hypothetical protein	NA	NA	NA	NA
WP_140858560.1\|7680151_7681373_-\|transposase	IS3 family transposase	A0A1B0Z042	Pseudomonas_phage	1.4e-59	47.0
WP_162520988.1\|7681980_7682292_+\|transposase	transposase	NA	NA	NA	NA
WP_174258948.1\|7682340_7683693_+	hypothetical protein	NA	NA	NA	NA
WP_140856968.1\|7684178_7687481_-	hypothetical protein	NA	NA	NA	NA
WP_140856970.1\|7688841_7690158_+	DUF1214 domain-containing protein	M1HNU9	Paramecium_bursaria_Chlorella_virus	3.7e-53	32.2
WP_140856972.1\|7690523_7690709_+	hypothetical protein	NA	NA	NA	NA
WP_140856974.1\|7690871_7692830_-	phosphoesterase	NA	NA	NA	NA
WP_140796666.1\|7693526_7694270_+	UTRA domain-containing protein	NA	NA	NA	NA
WP_140856976.1\|7694285_7695152_+	TSUP family transporter	NA	NA	NA	NA
WP_140799859.1\|7695148_7695466_+	DUF1634 domain-containing protein	NA	NA	NA	NA
WP_140856978.1\|7696016_7697024_+	hypothetical protein	NA	NA	NA	NA
WP_140796667.1\|7697298_7698636_+	hypothetical protein	NA	NA	NA	NA
WP_140799861.1\|7698672_7699989_+	DUF1214 domain-containing protein	M1I2Z8	Paramecium_bursaria_Chlorella_virus	9.8e-54	33.0
WP_161606799.1\|7700257_7700779_+\|transposase	transposase	NA	NA	NA	NA
WP_140795588.1\|7701896_7703324_-\|transposase	ISKra4 family transposase	NA	NA	NA	NA
WP_140856980.1\|7703465_7703708_+	hypothetical protein	NA	NA	NA	NA
WP_140856982.1\|7703901_7705887_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_161606800.1\|7706223_7707009_+	anti-sigma factor antagonist	NA	NA	NA	NA
WP_140856986.1\|7709049_7710804_-	cadherin-like domain-containing protein	NA	NA	NA	NA
WP_161606801.1\|7711021_7712143_+\|transposase	transposase	NA	NA	NA	NA

DBSCAN-SWA_10

7742427 : 7810947

Rathayibacter_phage(25.0%)

tail,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_161606804.1\|7742427_7742739_-\|transposase	transposase	NA	NA	NA	NA
WP_161604932.1\|7742730_7742913_+\|transposase	transposase domain-containing protein	NA	NA	NA	NA
WP_140795129.1\|7742917_7743343_-	hypothetical protein	NA	NA	NA	NA
WP_140857006.1\|7744173_7744923_+	NmrA family NAD(P)-binding protein	NA	NA	NA	NA
WP_140857008.1\|7744937_7745438_+	Ohr family peroxiredoxin	NA	NA	NA	NA
WP_140796671.1\|7745539_7745944_+	cupin domain-containing protein	NA	NA	NA	NA
WP_140800804.1\|7747062_7747602_-	hypothetical protein	NA	NA	NA	NA
WP_140795133.1\|7748587_7750000_+	aminotransferase class V-fold PLP-dependent enzyme	NA	NA	NA	NA
WP_140857010.1\|7750241_7750541_-	hypothetical protein	NA	NA	NA	NA
WP_140858568.1\|7751010_7752006_+	PQQ-binding-like beta-propeller repeat protein	NA	NA	NA	NA
WP_140857012.1\|7752666_7754814_-	hypothetical protein	NA	NA	NA	NA
WP_140795137.1\|7754939_7756967_+	lipoxygenase	NA	NA	NA	NA
WP_140857014.1\|7756987_7758424_+	cytochrome P450	NA	NA	NA	NA
WP_140857016.1\|7758420_7759266_+	fatty acid desaturase	NA	NA	NA	NA
WP_140857018.1\|7760351_7761710_+	peptidoglycan DD-metalloendopeptidase family protein	A0A1P8VV77	Rathayibacter_phage	3.2e-15	38.3
WP_140858570.1\|7762522_7764202_+	hypothetical protein	NA	NA	NA	NA
WP_161606805.1\|7764563_7766018_-	S8 family serine peptidase	NA	NA	NA	NA
WP_140795142.1\|7766457_7767222_+	hypothetical protein	NA	NA	NA	NA
WP_140795143.1\|7767387_7768815_+	hypothetical protein	NA	NA	NA	NA
WP_140857022.1\|7770968_7772726_-	DUF5050 domain-containing protein	NA	NA	NA	NA
WP_174258949.1\|7772901_7773066_-	hypothetical protein	NA	NA	NA	NA
WP_140795145.1\|7773333_7775754_+	tandem-95 repeat protein	NA	NA	NA	NA
WP_140857024.1\|7775902_7778260_-	hypothetical protein	NA	NA	NA	NA
WP_161606806.1\|7778273_7779287_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	9.6e-25	32.4
WP_140857028.1\|7779316_7779814_-\|transposase	IS66 family transposase zinc-finger binding domain-containing protein	NA	NA	NA	NA
WP_140857031.1\|7779860_7780226_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140858573.1\|7780229_7780544_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_140857033.1\|7780658_7781288_-	violacein biosynthesis enzyme VioE	NA	NA	NA	NA
WP_140857035.1\|7781421_7782711_-	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_140857037.1\|7782711_7785723_-	iminophenyl-pyruvate dimer synthase VioB	NA	NA	NA	NA
WP_140857039.1\|7785755_7787024_-	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_161606807.1\|7787501_7787855_-\|transposase	transposase	NA	NA	NA	NA
WP_140795157.1\|7792060_7792594_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_140795158.1\|7792580_7793132_+	hypothetical protein	NA	NA	NA	NA
WP_140800808.1\|7793326_7793719_+	hypothetical protein	NA	NA	NA	NA
WP_140858577.1\|7793956_7795375_+	TolC family protein	NA	NA	NA	NA
WP_140857041.1\|7795371_7798515_+	efflux RND transporter permease subunit	S5VTK5	Leptospira_phage	1.0e-61	22.6
WP_140795160.1\|7798516_7799620_+	efflux RND transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_140857043.1\|7800055_7801450_+	hypothetical protein	NA	NA	NA	NA
WP_140795161.1\|7802945_7803230_+	hypothetical protein	NA	NA	NA	NA
WP_140857045.1\|7803373_7804765_+	ammonium transporter	NA	NA	NA	NA
WP_140795163.1\|7804839_7805523_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_140799898.1\|7805685_7807656_+	protein kinase	A0A2I2L4T9	Orpheovirus	8.7e-14	27.9
WP_140795165.1\|7807570_7808521_+	hypothetical protein	NA	NA	NA	NA
WP_140795166.1\|7808535_7809360_+	hypothetical protein	NA	NA	NA	NA
WP_140799899.1\|7809438_7810947_-\|tail	tail fiber domain-containing protein	NA	NA	NA	NA

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP017169

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection