CRISPRimmunity

Please click to download your results

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_CP017172	Myxococcus xanthus strain KF4.3.9c1 chromosome, complete genome	20 crisprs	cas3,WYL,Cas9_archaeal,csa3,2OG_CAS,RT,DinG,cas2,cas1,cas4,cas7,cas8c,cas5,DEDDh	5	57	11	1

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP017172_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_1

217425-217732

Orphan

Consensus_repeat	Method
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP017172_1

>merge|NZ_CP017172|1|217425-217732|CRISPRCasFinder
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGCCAGGATCTGCTCCTGCGTGAGGTCCTTGAAGCCCAGCTCGCGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGCGATGACGTCATCCGAATCCGTGCTCTGGAATCCCAGTTCGCGCATCTGCTTCACGAAGTCGGGCGTGACGCCGTGGATGCCCATGGCCATCAGCTGATTCCAGGGCAGCTTCGTGAAGCCGGCGCCGGCGAGCTCCTTCACGCGCTGGGGCGTGACGCCGTGGATGCGGCCCTC

>NZ_CP017172|1|1|217425-217732|CRISPRCasFinder
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	CAGGATCTGCTCCTGCGTGAGGTCCTTGAAGCCCAGCTCG
CGCATCTGCTTCACGAACTCGGGCGTGACGCCGTGGATGCGGAAGGC	GATGACGTCATCCGAATCCGTGCTCTGGAATCCCAGTTCG
CGCATCTGCTTCACGAAGTCGGGCGTGACGCCGTGGATGCCCATGGC	CATCAGCTGATTCCAGGGCAGCTTCGTGAAGCCGGCGCCG
GCGAGCTCCTTCACGCGCTGGGGCGTGACGCCGTGGATGCGGCCCTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140796920.1\|211924_212344_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140872981.1\|218401_220525_-\|M56-family-metallopeptidase	unknown	unknown	gnl\|CDD\|320700
NZ_CP017172.1\|WP_140786652.1\|221066_221882_-\|sterol-desaturase-family-protein	unknown	unknown	gnl\|CDD\|377224
NZ_CP017172.1\|WP_140800574.1\|216759_217170_-\|fibril-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259159.1\|225182_228041_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP017172.1\|WP_174259160.1\|228274_229999_+\|GAF-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_026113917.1\|220521_220917_-\|BlaI/MecI/CopY-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367747
NZ_CP017172.1\|WP_174259400.1\|207435_208650_-\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223523
NZ_CP017172.1\|WP_140786654.1\|222513_223617_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_090490981.1\|232590_233106_-\|GreA/GreB-family-elongation-factor	unknown	unknown	gnl\|CDD\|334464
NZ_CP017172.1\|WP_140872980.1\|212356_213058_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140786653.1\|222160_222505_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140872979.1\|208857_211560_-\|AsmA-family-protein	unknown	unknown	gnl\|CDD\|282957
NZ_CP017172.1\|WP_140796922.1\|214819_216751_+\|DUF885-family-protein	unknown	unknown	gnl\|CDD\|377577
NZ_CP017172.1\|WP_140872977.1\|206116_207406_-\|sigma-54-interacting-transcriptional-regulator	unknown	unknown	gnl\|CDD\|226350
NZ_CP017172.1\|WP_140872975.1\|203662_204544_-\|TSUP-family-transporter	unknown	unknown	gnl\|CDD\|376667
NZ_CP017172.1\|WP_174259161.1\|230003_232520_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_140786643.1\|205169_205874_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293810
NZ_CP017172.1\|WP_140786655.1\|223632_225069_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238742
NZ_CP017172.1\|WP_140872976.1\|204540_205152_-\|rhodanese-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|238089

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140872981.1\|218401_220525_-\|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.	4.14119e-53
NZ_CP017172.1\|WP_140786652.1\|221066_221882_-\|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_CP017172.1\|WP_090490981.1\|232590_233106_-\|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.	5.00573e-13
NZ_CP017172.1\|WP_140786655.1\|223632_225069_-\|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_CP017172.1\|WP_140872979.1\|208857_211560_-\|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.	2.70967e-10
NZ_CP017172.1\|WP_026113917.1\|220521_220917_-\|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_CP017172.1\|WP_174259159.1\|225182_228041_-\|PAS-domain-S-box-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	1.72276e-61
NZ_CP017172.1\|WP_174259400.1\|207435_208650_-\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|223523	COG0446, HcaD, Uncharacterized NAD(FAD)-dependent dehydrogenases [General function prediction only].	3.89931e-35
NZ_CP017172.1\|WP_140796922.1\|214819_216751_+\|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_CP017172.1\|WP_140872977.1\|206116_207406_-\|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].	5.80846e-133
NZ_CP017172.1\|WP_140872975.1\|203662_204544_-\|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.	3.95258e-33
NZ_CP017172.1\|WP_174259161.1\|230003_232520_-\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.22384e-56
NZ_CP017172.1\|WP_140786643.1\|205169_205874_-\|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.	1.75504e-82
NZ_CP017172.1\|WP_174259160.1\|228274_229999_+\|GAF-domain-containing-sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	5.18494e-53
NZ_CP017172.1\|WP_140872976.1\|204540_205152_-\|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.	2.29121e-22

>NZ_CP017172.1|WP_140800574.1|216759_217170_-|fibril-protein
MLFLAACASTNKSAVPEPRASASTAPRVEVVEYGFHPQDPVRVGWGDRGMMAFLELLRGPQGQRIAWRRVGPCCGAGAPTELEVFEVTYDGLAAPVSLYLDPNTAGAVHAPNGFSIQGLASRSQVEQEETPRVIEL
>NZ_CP017172.1|WP_140796922.1|214819_216751_+|DUF885-family-protein
MRDSRPPRTPRRTRMGTFSRQLGRELFDGESSRPRFPLSEPPFNHETRRAMRIRSAFVLLACVSACASRSGAGPESSTAMPTASVSAADADYVLLAREYLDWYAAANPTRATRLGYHMHDAHLPDVSSDALKRKAEALRGWLTRLEQAVARGGLSGDAAVDVRVLENAMRADLLELEEVRPWERNPGFYVGIISSGLDGLSSREFAPVAERMRAMRSRMARIPGVLDAAQFNLSGVPKLWAEYALRDARGTVAYLRTDLPRALAAQGYAQVPLSERAAFSAAREEAARQMEAFAVWLERELLPKADGDFRLGRERFEKKLALEEHVTLDADALRDINERAIRDYKAWVAREAARLDASKTPEQVMAELVKDHPKAEELVASARAQLVELQRFVRERNILTLPSDRLPVVRETPPYARLGFASMDTPGPFETKATEAFYNITNVEPGWTPEQKAQHLTYFNRAGLLGITVHEAMPGHFVQLLYGARIPTDVRKVFTPASLVEGWAHYSEQMMVDEGLGNGDPAVRLGQLRRALQRHARWYAALALHVYGEPVEAVAKRYAEIAYFEPFPALREVERGTLDPTYLYYAVGRMQIFKLRDDYRRHLESRGKTLVLKDFHDRLLQLGLPVSLAREVFLPGDTAPSLE
>NZ_CP017172.1|WP_140872980.1|212356_213058_-|hypothetical-protein
MRMHWTGRASCWRRWDREANRIAGGAVLTLALSCSGNLRHAQETESYGFMSIDSGYVWARGPWPEVQASSDPDEVIDQLCPAIMRLDRATARDFGQEYCGVIYSRGDGIYRTTHPSPLGEPQLRGETKQKSCFPVRRVVDPEAKVTPILADFHSHPWFPSPLSQQDKMAANQLYFLKIQFDSACQIQKIIPYLDRPDAPGEVYSRRGKRWVLIGIIKPSNKAAGIVTPVGGLD
>NZ_CP017172.1|WP_140796920.1|211924_212344_-|hypothetical-protein
MTRWLPFLILALPACALFQRPPRPVHAPPEEAARFAFPPTGIPEEGLRSIPGDMARAIQLAMEDFYPWDKKVPTPSHPGRECLYRRESYDVYAAPYQEGVVLVSIVLSPQACGAQAVPNDMGALYAVDTRGWRILAVQH
>NZ_CP017172.1|WP_140872979.1|208857_211560_-|AsmA-family-protein
MSDTVVKKKRRWPYVLGGVFALLVIVVAVALWRLDAILLKTARDQAATYSQLLGRPIEIGDISTKLFPTIGAQVENVTVGPAEGEDLPLAQLALIDVRVAAGPLLSSSGKDIQVKNAEVSGLTVNLVRFADGTTNVQRLLQRLEEQQPKEEEAPAEESQPMDLSGVHVERAALTDGAIRFVDRGAGAQARELGVKDLDIEVKDLRVGKPLVVNLAAAVLADTQNLQVSLHAAPLPATLVPTPERVTLKAQKIDLAPLGPFLPPDIGLQAGTLDADWQADLGGAVPGGQGPTKLVGIIKALGLSFTGSEGGKALDVVMDTDVAGDITTGDLALNKLKVDLGPASLTGKGSVKGLLTDKPAVEGFELTGRNLDPAALAEYYPPLRKQLNGMIAGPIGLDVRGSGTQDAQAIDVNVDLTPVRLRVPAQLTKDAGGAMKLSARVSGAAATGGALRFDAKADLGGIDLRPGLLVDKAPGQRMDLSAAGTYAPGKGSGMKVDIPKLTANVLADTMTGSASFALAGSGKKQTTTFSADLKSQKLDADALMMSEEEVQARGGPPPEEPPSDDPTRFNGYRGDIRFAVGTLRYMEMNMTHVTGVVKMTDDLIAVEKFSTGVYGGRIVADGTTVRLGPLPEQRPFEAKVKVEGVAVEQALTQFTPQKAVTGKFNGNVDVKGVGYTPDQLKQTLLGGIHGDLLDGELLGKDLVSAVSEPLAKALPIAAKGLKNEQVTKLGGDLPFSVQIKNGVAQLSKPLTWSRPEAELSFDGGIRLDGALDLTGSVSLSPSTVKTLTLGKVTPPAAIPVGLKLTGPAWKPEVTSLDVKPAVTQIAKLAASSLAGNLIGGERGQQVQGLIEGGEDKLRAEAEARRRELEAKAAEEKARLEAEAKKRAEEEAKKRLRGLFGK
>NZ_CP017172.1|WP_174259400.1|207435_208650_-|NAD(P)/FAD-dependent-oxidoreductase
MVPVREHHRVLIIGGGTAGIAVAARLARAGQKGVAVLEPSQHHYYQPLWTLVGAGEARIEDTVRNESRLIPRGVKWVRDAATEIDPEAREVHTRGGLRLGYDFLVVAPGIQLDWDKVAGLREALKTPHVSSNYDVQLAPKTWRLLQNFQGGTALFTQPSTPVKCAGAPQKIMYLAADHFRRTGVLERTSVVFGSGAKTIFGVKPFASVLEGVVHRYGITPRFQHNLIAVDGERREATFEAPRDGQTERITLAYDMMHVTPPQSAPDFIKRSPLSWQEGPNAGWVKADKYTLQHPDHPNVFALGDASDLPTSRTGAAIRKQAPVLVENLLACMKDLPLPARYDGYASCPLTTGYGRLLLAEFDYDGKPAPTIPFIDTMQERRDMWLLKKYGLPRLYWAFMMRGLA
>NZ_CP017172.1|WP_140872977.1|206116_207406_-|sigma-54-interacting-transcriptional-regulator
MPTSHLALPALDALAGPVLLVDDARKVTALTPALEALLGGTLRAGTPLAQVLVRADGAAEQLDAVLKNGREASVRLRVGGRSKPVRVRAVPLARGPRASGWALLLSPDAEEETNGRAELFHGLWTQAPELQRVFRIVEKVARTESSVLVRGESGTGKEHIAHALHALSARARGPFRAINCAALPPNLLESELFGHVRGAFTGAVRDSPGHFRLADKGSLFLDEVAEMPLDLQAKMLRVLETRTVIPVGGRQPVPVDVRIIAATHRPLRREVEAGRFRADLMYRLRVVPLFLPTLRERRGDILPLALRFLEELHQRGARRVERFSPGARRLLEEHPWPGNVRELRNVMEYAYVIGEGPVVREADLPPEFSEPRQAIPVTQPPLDASLEPERIRAALAQAGGNRSEAARLLGVSRVTLWRRLRDLGASVER
>NZ_CP017172.1|WP_140786643.1|205169_205874_-|MBL-fold-metallo-hydrolase
MLFRQLFDADTSTYTYLLADEATGAAALIDPVLEQTERDLKLLRELGLTLSVVLETHVHADHVTGAGVLRERTGATVVASSRGAPCVDQTVHHGDIVRVGGLEVRVLETPGHTDDSLSFLCERRLFTGDALLIRGTGRTDFQNGDPGQLYDAITRVLFTLPDDTVVYPGHDYAGHAVSTVGEEKQHNPRLAGRTRADFIVLMNALQLPPPRKLDVAVPANRACGHTPPSPSLQA
>NZ_CP017172.1|WP_140872976.1|204540_205152_-|rhodanese-like-domain-containing-protein
MHPLFDNATPHPAGYRDVDVGQLAACLPSELTLVDVREAAELDGILGHVAGIRHAPLATVPDVVDTWPRDTDVVLICRSGARSARAATSLVTLGFTRVMNLRGGMLAWNTARLPVVRPVPHTLPTLGTVRDGLLDGLHRALTPPPHEAPTVPPMTTPSREALTAVLDALQAARPTGVRDAAAFEHLLRTYRDLLAAARAEGER
>NZ_CP017172.1|WP_140872975.1|203662_204544_-|TSUP-family-transporter
MMLYAGIAGSLLVGILLGLLGGGGSILTVPLLIYVLDVEPRTAIAMSLVVVGVTSASGAFLHARAGRVRWRTALVFGTGGMGGAFLGGRLNPHLEPDTLLLLFAGVMVAAAVAMLRRREAGPVAPSVPPLPAPRVLAQGIAVGVLSGLVGAGGGFLIVPALSLAGLSMPVATATSLVVIALQCAAGLVGHLGHLDLPWMLTGEVLLAAMTGSLVGGRLAGRVPPALLRKGFAVFVLTTAAFILSAQAPAPLRERVWTEGLWLWSVAPLAVGIPVMVWRLRVARQRQTAQALPR
>NZ_CP017172.1|WP_140872981.1|218401_220525_-|M56-family-metallopeptidase
MSRLLMESLGWALLHSLWQGTLVALMLAVALITVGRRAAHARYALACGALVLALALPMASGWKHFHGAPARVAMDLSVPRAQLRVDDANPPPVKDTAARPAWRLSPVAASPAWIDADMAEDGAASGFESTVLTGLGSFLVMAGLLLQRALSQVEAHLHWLVLAWVAGVGLCSGRMAAEWMKLRRLADRALPAPEAWQERLDALSRRMGLRRAVRLLQSSDVDVPAAVGWLSPVVLLPVSTLSGLPARQLEMVLAHELAHIRRHDFAVNLAQVLVETLLFFHPAVRWISHVIRVEREHCCDDVAVAASGNSVSYARALTALETLRVLPGTPSPAMSALGGSLPERVRRLITLPTSRCASRWAAGASVLTLVSSLAVAAPLTSLLLGQTDTAPRPGDEPVLVQAPPIPALSRTPPVPPAPLPVAPPAPPAPPAPPAGVAAVAARVAPASAPSPAPQARSLGSRAQRELDRQTRVGAGQQLSVAQLIALKNAGITPERVQQLTAMGYTPTVSNLVMMTHAGITPDYVQDMNTRFGRKLEVKELTHLRHLGVTPDYIQSLKSAGFNIDDPKALSHARAVGVDEDFVRGLKDAGYTGMSLEELAHLRAVGVSPEYIREMNKHGLSKLKARELMQLRAVGVDPGWLASMRKAGVQTTDAKALQRLRATGVDADFLGELHDAGLKDLSVDELVRLRTGGVDADFIRKMRGTDSK
>NZ_CP017172.1|WP_026113917.1|220521_220917_-|BlaI/MecI/CopY-family-transcriptional-regulator
MSETKLPRPTDGELAILRVLWARGDSTVREVHEALTRDEPEGTGYTTVLKLMQIMTEKGLVERDESQRAHVYRPRATEQRTQRQLVTDLVDRAFGGSPARLAMQALSSKKTRPEELAELRRLLDTLEGGEE
>NZ_CP017172.1|WP_140786652.1|221066_221882_-|sterol-desaturase-family-protein
MAVSAPFSFLKNRKHNLDRMTLGDLVYSFFTYYAVVAYITVGIISLALAVKWFENPLRMLLAMLAASVAFPFGWYLVHKHILHSRFLYKSPLTAATWKRIHFDHHQDPHDLRVLFGALANVLPTVGGVIAPIGYLIGGKAGAAAALGWAMVITCFYEFCHCIQHLNYTPKSQFLKDIKRLHLSHHFHNEQGNYGITNYFWDRLFGTFYEKSGDKPKSPTVFNLGYTAEEAQRYPWVDRLSGGTRGDGHPRRFWEDQAAAQTPPEPTTRQDS
>NZ_CP017172.1|WP_140786653.1|222160_222505_+|hypothetical-protein
MTFREARMAEHEGQQTPRTKVRRRRTSTPKTVRTGERSAGPDRGSIALRRTASEYRATAEEQAARVREEIEAALVQARSTREAIEQRIADQLHAPPVRHTPPPRRKRTTRASRK
>NZ_CP017172.1|WP_140786654.1|222513_223617_-|hypothetical-protein
MALSVQYFHREEFETRTLRALGGAACMGLVAGAVPDLHLTPEYVAIVAAAQACVKPTGVHPLALRLALTVLPALPYFFRAPEPLPVSLAGALAAALVAWLGHGREQPGQPAAVATSAAAAGVLVPLGLYVQQVLEARFLGSDGLLSALVGFLVVGLFWSIGTLPANLRVELDAVEARGRQLQDALKGDSRTLATRALTLYRQCKDAVTKMPPSTGRTELLGVLEKMTGDSFSLAEVHFGLEAQLGSVVANDVDAQVRELRERAAATQDAVARRQLELAASSLGEELNHLDVLARRKERLLAQLHAQVALLERARVSFIGVQGNELGAKGAQAADLARKLKQLGEPASSTGPEDVAPVAAPNPTRVAP
>NZ_CP017172.1|WP_140786655.1|223632_225069_-|VWA-domain-containing-protein
MNRSLLLVAATGVLAVGALLLGTPPTPPGPPPPAVTDTSHTVRRPEDPPATRTLTLVTSKPEDGALNMAGKLSGAYVQTGPSEAFAWLELKARPAETGQRVPVSLALVLDRSGSMNGQKLADARRAATELVQRLKPEDRLAFIDYGTDVRVQPSRRMTEEAREELLTLISGLQDDGSTNISGALDAAANALRPHMREYRVSRAILLSDGQPTTGIVSEPGLLDQVRQLRRDGITVSALGVGRDYQETLMRGMAEQGGGFSGFIDDSARLAEVFSRELDQATSTVARLVELRLDVPPEVQHVEVMGMASFREGNVLKVPLYDMASAQTVRIMAKLTLNTPRTTGALALLNARVHYVDVARDMPTETALRLTAEVTSDLDLVREHLDKEVRVHATRALGTQHMVAAAEEMKRGNKAKARSLLDNARTIFGSSADALSGELADVNRSQAALAGASSAEEAQAESRNLLKKSIKNFGQNNTY
>NZ_CP017172.1|WP_174259159.1|225182_228041_-|PAS-domain-S-box-protein
MQKPHSTPDWTSREHRYRGVIDSLREVVFQTDLAGTWTFLNPAWTDITGFSVEESLGRSFSDFLHPDDRERDPEPLQKLFAGEVEFVRHEMRYLTRDGSYRWVEVFARLMHDDDGGILGTAGTLNDFTERKAADGALARRERYLTALVDMQQRLLATQDGGDLYGPALAPLGHASGASRVYVFELHRAQDGAVLSSQRAEWCAPGVKPEIDNPDLQNVPMEPALRRWTETLSRGDVIEGLVESFPAPERELLEPQGILSLLVLPLRVRGVLTGFVGFDNTSEARRWDRLEVDLLSAAAGAISMALERRESERALRERERRFRQLAENASDVLYVYRREAPRGFAYVSRVAHTKLGYGPVAHYADAELWYRRVHEEDRALMEQLLEAPEPFQGAPVVVRFLHPDGRTLWLEHVVAPVTDASGRMVAVEGLARDITVRRQAEEALRLSEASFRALLEGVPDAAAIERDNQIVYANAALVATLGFERADQLVGRPLTEFVRDMRSPDAVRAGALTGERRLVRRDGRTRVAEVVSLPLRFDGQPAVVSIARDVTEQRQLQARLTLADRLASVGTLAAGIAHEINNPLAFVLSNLGFLSDEFNRSLPPGDGAAALQARLKGEPDLGEWQEVLQEACEGAERVRQIVRQLKTFSRPDEERVSPLDVHAVLESVAMMAANEIRHRAQLRRDYGDIPPVMANEGKLSQVFLNLVVNAAQAIPEGAAHRHEIRLATRVDGAGRVVVEVADTGVGIAREVIDRIFDPFFTTKPVGVGTGLGLSICHSIISGLGGDITVDSEPGRGTLFRVVLPTPETVERAKPSEPDSRQAPHAPRGRVLVVDDEPAVGRVLQRILREHQVDVACSGRQALELLERGLAPDAVLCDVMMPDLTGRDVYEAVRREYAGLERRFVFVSGGAFTSGARDFLASIPNLLLEKPFDEARVRGVVEELVRQRQPAHDA
>NZ_CP017172.1|WP_174259160.1|228274_229999_+|GAF-domain-containing-sensor-histidine-kinase
MASGSAPLSMTHLDSEEADALLKEGVLRLLLEQAGEALVLVDVTGRVLAFNVEAGRQFRMSRPERAEQGWLPGCVWTRAEDASMSVEVPPLARALTGEWVAEARWRVRRPDGTHVLLRASAVPLEHDEGPTAGALLRACEVASSVGLDAVGSARLLAEAGALLGAAFDDEAAPRLLRLLVPALADAAVLYLGLPGGPPRPVTALHAEPERHGLLEEALRRYPLPPERVLPLFGTGQSERLRVTEAHVEAAARDAEHARLLRGLGLRCYLGVPLVARERVIGTLALFRADEARDFSAEELRLAEEVARRTALSVDNAQLLQEAREAVRLRDEFLGIASHELKTPLTPLHLKVQLLQKQVDGMAAHNQPVSAERVSETLEVVQRQVRKLTSLVDNLLDVSRITAGRLRLEVEEMDLASVAAEILYRFAPSASQLQCELELHAPVPVMGRWDRLRLEQVVTNLLSNALKYGAGHPVRVAVEAEGLTARLTVRDGGIGISAEDLPRIFERFERAVSDRHYGGLGLGLYITRQIVEAFGGTVRATSEPGQGSLFVLELPRGDIPEEWLTAHGAPEPSSS
>NZ_CP017172.1|WP_174259161.1|230003_232520_-|HAMP-domain-containing-protein
MSSSPSPQIQAPSPPALLPLTWPAAVVGLMFGVLMTYVPYEFRVASFRPLYPYVRVLGLTYLTGSIMLMGALLYPRAPRWLDVTGRLLLGAAMALYWWVLNVLPGSFTGIILYPVLFGGVVLEAWPAMRQRPVLRTFAALTGAAFGVAMLVVPERFPLSVYAHLAPLRPLVGLLFAVCGVGLLLPSHRLHRQLPALFMGGLAVPFALLAYALGRGASWLGASVYAVLTLACVAQALDWRPRAPRTVGWKLLRGLAFAGLVPLLALGGLAAYLAQNAIEQQVRDDTQRAAAGEADFLRRYLDDAGESLALMLESPGFRAAFAAAAPERLEPYLVNLAAQERAFDAALAVDTQGHILAASPSVEGWNLEPRDFLPPAFTRGAEVSPPFIRPPGQPLVAVTQPFREDGEVRGMLVGLLSLERLSQATTPASRRFRVQVLDRRGLKVLRDTAPGAPLLGEAHLPDALSLELLRPGIGVLEAFDAADRRMLAAEAPVEGTEWSVLVTQELVVAYAAITRMSAAVVGLVLLGVLMALLLSQLVARDVIRRLDHLRTATAALTAGDWSQRVDVEEDDELGELARGFNEMAARTGATQTELKEAVRAREEFLSVASHELRTPLTPLKGFAALTLQRLEKSGDFPERERLLKALRSMARQTERLTRLVDDLLDTARIQGGRLELERKRMDLAPLLGEVLERFELRTESGVTFELDVPSHPVEGDWDALRLEQVLTNLVSNAVRYSPHGGAVRMSLEAAETHVLLSVRDEGIGIPPENVADLFRPFARASNAQARHFGGLGLGLFICREIVERHGGTIWAESPGPQRGSSFHVRLPRRAEPAASASAA
>NZ_CP017172.1|WP_090490981.1|232590_233106_-|GreA/GreB-family-elongation-factor
MRLDKHALLGQLADRLQQSDRLAHRAEAEAREAARSLATESEKKEDGRAALEFGSLATGQAQRARRVQEELQALTKFGQAEFPRFPRQGPVALGAIVDVSTEDEEGFSERTFFVLPAGAGTELTGPGGDGFLSVITPASPVGRALMGRKAGDTVEVMLAGEVREWTVLEVA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_2

403459-403565

Orphan

Consensus_repeat	Method
GCTGCTGCCACCGCGTCCCCAGCCGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_2

>merge|NZ_CP017172|2|403459-403565|CRISPRCasFinder
GCTGCTGCCACCGCGTCCCCAGCCGCCGCCGCTGGAGCCCGAGCTACTTCCGCTACGGTTGCCGCTGCCGCTGTTGCCGGAGCTGCTGCCACCGCGCCCCCAGCCGC

>NZ_CP017172|2|2|403459-403565|CRISPRCasFinder
GCTGCTGCCACCGCGTCCCCAGCCGC	CGCCGCTGGAGCCCGAGCTACTTCCGCTACGGTTGCCGCTGCCGCTGTTGCCGGA
GCTGCTGCCACCGCGCCCCCAGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_174258605.1\|407653_409084_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017172.1\|WP_140786782.1\|394075_395131_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140786791.1\|412683_413007_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259168.1\|396883_398515_+\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|271154
NZ_CP017172.1\|WP_140786790.1\|406585_407575_-\|RimK-family-alpha-L-glutamate-ligase	unknown	unknown	gnl\|CDD\|182468
NZ_CP017172.1\|WP_140796300.1\|391931_393836_+\|KUP/HAK/KT-family-potassium-transporter	unknown	unknown	gnl\|CDD\|225700
NZ_CP017172.1\|WP_140796302.1\|409285_410023_+\|pilus-assembly-protein	unknown	unknown	gnl\|CDD\|377921
NZ_CP017172.1\|WP_140786784.1\|395734_396472_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|224682
NZ_CP017172.1\|WP_140873033.1\|390103_391597_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_140873038.1\|413774_416675_+\|isoleucine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235588
NZ_CP017172.1\|WP_140873037.1\|404693_405683_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259169.1\|410019_411663_+\|Tad-domain-containing-protein	unknown	unknown	gnl\|CDD\|379164
NZ_CP017172.1\|WP_140796999.1\|389523_390069_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140873035.1\|399612_402222_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|380161
NZ_CP017172.1\|WP_140873036.1\|402295_403279_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140786792.1\|413049_413739_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174258603.1\|395141_395723_-\|DUF2378-family-protein	unknown	unknown	gnl\|CDD\|131318
NZ_CP017172.1\|WP_140873034.1\|398522_399623_+\|PD40-domain-containing-protein	unknown	unknown	gnl\|CDD\|274305
NZ_CP017172.1\|WP_140786789.1\|405748_406420_-\|DsbA-family-protein	unknown	unknown	gnl\|CDD\|225355
NZ_CP017172.1\|WP_140796304.1\|411662_412682_+\|pilus-assembly-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140873033.1\|390103_391597_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.17202e-53
NZ_CP017172.1\|WP_140786790.1\|406585_407575_-\|RimK-family-alpha-L-glutamate-ligase	gnl\|CDD\|182468	PRK10446, PRK10446, 30S ribosomal protein S6--L-glutamate ligase.	2.14698e-91
NZ_CP017172.1\|WP_174259168.1\|396883_398515_+\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|271154	cd14488, CBM6-CBM35-CBM36_like_2, uncharacterized members of the carbohydrate binding module 6 (CBM6) and CBM35_like superfamily. Carbohydrate binding module family 6 (CBM6, family 6 CBM), also known as cellulose binding domain family VI (CBD VI), and related CBMs (CBM35 and CBM36). These are non-catalytic carbohydrate binding domains found in a range of enzymes that display activities against a diverse range of carbohydrate targets, including mannan, xylan, beta-glucans, cellulose, agarose, and arabinans. These domains facilitate the strong binding of the appended catalytic modules to their dedicated, insoluble substrates. Many of these CBMs are associated with glycoside hydrolase (GH) domains. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold. CBM36s are calcium-dependent xylan binding domains. CBM35s display conserved specificity through extensive sequence similarity, but divergent function through their appended catalytic modules.	1.88292e-47
NZ_CP017172.1\|WP_140796300.1\|391931_393836_+\|KUP/HAK/KT-family-potassium-transporter	gnl\|CDD\|225700	COG3158, Kup, K+ transporter [Inorganic ion transport and metabolism].	0
NZ_CP017172.1\|WP_140786784.1\|395734_396472_-\|metallophosphoesterase	gnl\|CDD\|224682	COG1768, COG1768, Predicted phosphohydrolase [General function prediction only].	1.60593e-51
NZ_CP017172.1\|WP_174258605.1\|407653_409084_+\|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].	3.15551e-130
NZ_CP017172.1\|WP_140873038.1\|413774_416675_+\|isoleucine--tRNA-ligase	gnl\|CDD\|235588	PRK05743, ileS, isoleucyl-tRNA synthetase; Reviewed.	0
NZ_CP017172.1\|WP_174259169.1\|410019_411663_+\|Tad-domain-containing-protein	gnl\|CDD\|379164	pfam13400, Tad, Putative Flp pilus-assembly TadE/G-like. This is an N-terminal domain on a family of putative Flp pilus-assembly proteins. The exact function is not known. The Flp-pilus biogenesis genes include the Tad genes, and some members of this family are putatively assigned as being TadG.	0.000827629
NZ_CP017172.1\|WP_140873035.1\|399612_402222_-\|PAS-domain-S-box-protein	gnl\|CDD\|380161	NF033092, HK_WalK, cell wall metabolism sensor histidine kinase WalK. This model describes WalK as found in Staphylococcus aureus (sp\|Q2G2U4.1\|WALK_STAA8). A shorter version, as found in Streptococcus pneumoniae, called WalK(Spn) or VicK, is not included. WalK is part of a two-component system and works with partner protein WalR.	2.33002e-52
NZ_CP017172.1\|WP_140796302.1\|409285_410023_+\|pilus-assembly-protein	gnl\|CDD\|377921	pfam07811, TadE, TadE-like protein. The members of this family are similar to a region of the protein product of the bacterial tadE locus. In various bacterial species, the tad locus is closely linked to flp-like genes, which encode proteins required for the production of pili involved in adherence to surfaces. It is thought that the tad loci encode proteins that act to assemble or export an Flp pilus in various bacteria. All tad loci but TadA have putative transmembrane regions, and in fact the region in question is this family has a high proportion of hydrophobic amino acid residues.	9.63436e-05
NZ_CP017172.1\|WP_174258603.1\|395141_395723_-\|DUF2378-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.	3.26924e-61
NZ_CP017172.1\|WP_140873034.1\|398522_399623_+\|PD40-domain-containing-protein	gnl\|CDD\|274305	TIGR02800, Protein_TolB, tol-pal system beta propeller repeat protein TolB. Members of this protein family are the TolB periplasmic protein of Gram-negative bacteria. TolB is part of the Tol-Pal (peptidoglycan-associated lipoprotein) multiprotein complex, comprising five envelope proteins, TolQ, TolR, TolA, TolB and Pal, which form two complexes. The TolQ, TolR and TolA inner-membrane proteins interact via their transmembrane domains. The {beta}-propeller domain of the periplasmic protein TolB is responsible for its interaction with Pal. TolB also interacts with the outer-membrane peptidoglycan-associated proteins Lpp and OmpA. TolA undergoes a conformational change in response to changes in the proton-motive force, and interacts with Pal in an energy-dependent manner. The C-terminal periplasmic domain of TolA also interacts with the N-terminal domain of TolB. The Tol-PAL system is required for bacterial outer membrane integrity. E. coli TolB is involved in the tonB-independent uptake of group A colicins (colicins A, E1, E2, E3 and K), and is necessary for the colicins to reach their respective targets after initial binding to the bacteria. It is also involved in uptake of filamentous DNA. Study of its structure suggest that the TolB protein might be involved in the recycling of peptidoglycan or in its covalent linking with lipoproteins. The Tol-Pal system is also implicated in pathogenesis of E. coli, Haemophilus ducreyi , Salmonella enterica and Vibrio cholerae, but the mechanism(s) is unclear. [Transport and binding proteins, Other, Cellular processes, Pathogenesis].	6.48893e-41
NZ_CP017172.1\|WP_140786789.1\|405748_406420_-\|DsbA-family-protein	gnl\|CDD\|225355	COG2761, FrnE, Predicted dithiol-disulfide isomerase involved in polyketide biosynthesis [Secondary metabolites biosynthesis, transport, and catabolism].	5.41801e-26

>NZ_CP017172.1|WP_140873036.1|402295_403279_-|carboxypeptidase-regulatory-like-domain-containing-protein
MFFGQRGALWPHGQHHRGVDQGTDGAWGGLPPREAVESFPAMMRPLLMVPCAVLGLSLGCGPGDYTPDPGVQTDDAEAVDLDNLRIGVSGTVDLLPEARRLLEARGLPLPSLEGAPLTAAEPLRLAVNDANATFGTAPAAADGAFTVRDVAVREMHLSLAVGAEAAGLVPAHTVIYDSAFTGARPRTDIIGARVWALPDAFHDALSVAVGESAIRGHTDNRAATLRDAGFVLGRVVDASGHPVAGAKVAPDGEALAGRIYYPTADLQGANQEGTGPDGLFVYVHSGADAEAFLLSVTGTDGYVPRNVGVAPGWGLVLTIHPGIHPPP
>NZ_CP017172.1|WP_140873035.1|399612_402222_-|PAS-domain-S-box-protein
MFRRRRARPEPMTGGAPTVRTHRCAALASDAGGKSATHLSLERLDRGPRAGASREEPCAFLGDATMNECWRPQRRSAAMARGIAWLATLGAPLVGALYLLGWAWDVEMLRPGVAGIPMTPVTGIAMVFGGAALGLRLRSRPFRHQDHTATACALVTMAIGAVSLLRDITGWDLGMERVMLRLLDGHASVLPRPSPLSATCMTLLGMALALPERSHSVRPRDTLVVLSLVSSTLGLNGLLMGPLLTVGTLPFLAERSMGLPTALTLMLLAVGTLCARPGLGLMSRITRDSLGGFLARRLVPVTLLGPSVLGMVLMLLHEVRAINLEAKLPIFATFVSAGGAALVLLSARALDHIEAHRQQATAALEASEARYRGLLETTPAPLLTVDAHGLLRFVNTEAERVFGYPREELLGREVEALIPEGLFGGRSLDTGLGEHAIQGRRKDGSPLSLEVRLSPVSGPEGPSVLAVVRDVTERERYLAKVQRAREEAEMQRSQVQALLDHTPVGIVFAEADGSGLVANPVAEQLLGRPLKGVRLKMMGNNPFVLTTDGKPVRREDVPIVRALLTGQLAGPEEFLILHPDGSRLPVLMTAAPVFGPTGKVRGVVSTAQDVTTRHELDRLREEYVSLISHDLRNPLHTISLRVGLLRRALREQNLEREESMTESIQRSVAWMSTMIEDLLEGSRLESQRDTLRREPRDLARFLEEVMERDVAPDVRERFHMEVPGALPPVWMDAARLERVVANLLSNAAKYSPGGQPITVRVQLQPGQVVVSVTDLGPGLSPEDAAHVFDKYYRTQKSSASDAKGLGLGLYISRLIIEAHGGRIWVESELGRGSTFRFSLPVAPPGANPLPPQVPDGQDPAAGDGSAVSA
>NZ_CP017172.1|WP_140873034.1|398522_399623_+|PD40-domain-containing-protein
MRGLERLQRSWPWRARCLTALAVLGVGCSGRCGGTSGPGPLSKEEAGAIPGAVIFLSERAGRKDVWKVSPDGVETQLTRGEEDVYPGPLSPDGKSLLVISAAEEGGLHRQQMRVLPLDGKSPAVPLHPPRARARNASWAPDGTWLVAESDAEGFSDVVRLEPREGVPEVRLTQVPQGCFEPAVSPDGKDVAFVCSREGDPEVYVANADGSGERRLTFFHHEDRTPKWSPDGKWLVIVSDRERKDRLYFLRPDGSDLRAVSGESFVGDEREAAWSPDGQRLVYVSRLPDGNARIWMVPVGGGAPVALTDGKHRDDMPAWSPDGKYLAFVSERQGDTDVYLMRADGSGQTRLTSAKGPDWLPRWAPTR
>NZ_CP017172.1|WP_174259168.1|396883_398515_+|N-acetylmuramoyl-L-alanine-amidase
MHVLRKTFAVTAAAMALAACGPQPETSPEETAPESQVPAGAVDDAARAVADAARRTPNELDAQFAKAAGEFNVPVSLLKAISYAETRWEHVRGEEEFEGRPAAFGLLALRGQLITDGAALAGVSADAVRDEPLANLRAGAALLSKYADEAGIDRADLGAWAPVAVRLTDISDPDIQAHYIHNDVYAVLREGAGAFTPAGKVAVSLDATQVEPKFALPKMQALAAGPDYAASIWRPSPNYNARPAGIGQQMVVIHTCEGGYSGCWSWLTNSSAGVSAHYVVNESGTEVSQLVRESSRAWHVAAAYRSSLNGGVKSNLNGRSTNDFSIGIEHGGYASSASFSTGMINTSAKLTCNITRDQGIPRDSYHIVAHGRLQPETRTDPGPNWPWSTYISKIRSECGDGGGGTNPVIVVDSNNANNDSSKGYIAVPSSWARGTSAGYYGNDYYYASTQPISEPAVFHFHMPAAGSRTIQAWWVEGTNRSPSAPFMITHAGGNSTVTVNQQTNGSKWVTLGTYNFNAGWNKVQLSRWATEGYVVMADALRIQ
>NZ_CP017172.1|WP_140786784.1|395734_396472_-|metallophosphoesterase
MRLFGIGDTHLPSTRQKDMHRFGWSEHPLPLQRAWDERVAPEDVVIVAGDISWATRAHEVMDDLAWLDARPGRKVLVRGNHDYWWGDSASKLRKLLEPFRTLEGFLHNNAVVMGPWVIAGSRLWTAPEAPPMPGGEMGDEAADTGYVERETRRLTASMEDAKKKEAASATPLVRVVAVHFPPVYANEKATAFSEPIEAFGPKVCVYGHLHAAGIAAGFTGERGGVRYVLASCDAAGFAPVLLDEV
>NZ_CP017172.1|WP_174258603.1|395141_395723_-|DUF2378-family-protein
MPSNKAELEARLAAVHPGDSVRGLFFKSVLSLVQQQAGLTALETVRAGALSAAYTDLLTYPARDFLTLLYRAADALEPLLGPEDAVFHACGEKDVTRFSTGPGMLIFGIISRGDPQKLFAGAQMGYGAAVSYGSRDYVPTGPTSGTLHMRRDMLPPAYHEGILTGALKVLGLQGTARATPRGIDSADYDIQWA
>NZ_CP017172.1|WP_140786782.1|394075_395131_+|hypothetical-protein
MSPGTPRPKSGQSMLLDIAPSSANSAVAPVSAWASSEQTLETLSGLAPHTLLTHADLYPRICVRDPYYALKDVTVMGEGEVVARIPVQQDPDAEAGPIGLGEAGRHLAILGSCASALMSPKDGQHFYLACGARGQWLRPEPMARATDLLWGLAKAEFTGRRTATAHTLLSLPDGTPFFRLEVDYSVLSAAAFTRLFGEARVDMRREPRRDDGVQRTPEEWARLRQNPYSKPLALRDWRPDGESLSATLGPVTAEMCKGHFALHPVMPVAVVASGMTRVATTLLRRLEGAPWARCMAKDVRLKADTLAYAGQTVTFGAVRSAHDGDAHTFTCQASVGERVVAELDVTYIRVD
>NZ_CP017172.1|WP_140796300.1|391931_393836_+|KUP/HAK/KT-family-potassium-transporter
MPGGEDVKKGPDTFKRSALLALGALGIVYGDIGTSPLYALRECFTGAHGIPPTPANVLGVLSLIFWSLIIIVSVKYLLLVMKADNRGEGGILAMMALVMQRQRAQPSHRSRPVLITLGIFGAALLYGDGIITPAITVLSAVEGLHVATSVFDPYVIPITLVILVGLFLVQRHGTSEIGAVFGPVMCIWFLTLGVLGAKELAHNPAVLGALSPWHAVELFRHNHLHGFLVLGGVFLVVTGCEALYADMGHFGRKPIQLAWFSMVLPALMLNYLGQGALLLRDASAARNPFFLLAPSWMLYPLVALSAVAGVIASQALIAGVFSLTRQAMQLGYSPRMEVVHTSAEEMGQIYLPGLNWALLVGVVALVLGFRSSSALASAYGIAVSTAMVITTLMAYVVARELWGVRRWVAIPVVGLFLVVELAFFGANAVKVADGGWFPLLMAIVVFTLMTTWKRGRDILAAKLRASSIPLKELLGSFGDHPPVRVPGTAIFMTGNAEGTPPALLHNLKHNKVLHEQVVLLTILSEELPHVPPSERVEVEPLEQGFVRVVARYGFMENPGIPDVLKRCREKGLQFQLMGTSFFLGRETLIPTKRPGMAVWREALFAWMSRNARSATSYFRIPPNRVVELGAQVEL
>NZ_CP017172.1|WP_140873033.1|390103_391597_-|PAS-domain-S-box-protein
MLEAILQVSPLAIHLMDLDGTVRLWNPAAERLFGWSREDVLDHRAPWATDARWEKFRRHLEQATQGVEPPCLELELHRRDGTPLHVELWTAPMPPSTTGPAQCLGMLVDVTERRRGEAHRRLLSEASEVLGSSLEQDATLEHLVRLAVPGCADSCRVFLEDAPGEVRCVVSAGLDAREPLDAGTPLVPDEAAVSRIIASGEPALHDAEPPSWLGVPLAWPGRKGAALVFSRTGRTFDARDMALARELARRASLALDHARQYHEARQAIRLREEFLAIASHELKSPISALQLQVQNLRTALERTPDTVPRERLHRGLDLVGRQAKRQAKLIDALLDVSRIHAGRLELNPEPVDLGALVREVAERFEPEMAGAGTHLTLTLPLEAHGHWDRLRLDQVLTNLMSNAMKYGRGNPVQVALSNTEAHVRLDVRDAGIGIAPEHLPRLFHRFERAVSGRDYSGVGLGLWIVREVVEAMGGHVTVSSELGVGSTFTVVLPRARG
>NZ_CP017172.1|WP_140796999.1|389523_390069_+|hypothetical-protein
MKRMLMPLRRSVLVLGVVLGAGVAMAERKQDAINMKIAFQSFNLEMTPEAVTGADFQVARSPGMLKGRGLKGNFALTLKDGSVEGAVGGAPVNLTVTKEGDAIVAKGGFGGRPVNLKLSPSELTIYVRDCTYRLKAENTNRFYTGRRSCDRAMTPDSEIWLPDEFLAASPEEKAAILFLAL
>NZ_CP017172.1|WP_140873037.1|404693_405683_+|hypothetical-protein
MAETEFTSGASCPLHPGFEAVGTCSRCGNFMCRTCGEGGSQAWCPSCRQREGVGQAFPLNRENWSVSGLMDLSWDAFKREWVMLCVGVLIFLAGSFAGQVVSQIFSVVSGLTGSVVVTVLGFIVGIIGSYAIQGAVTMGFLRMCMDVLSGRRADLTRMFSQFGKIPQYLGTLFLSFLLMLPLLLLIVVVALGAGLATGTLSWSELVALKDLPPSEMDAALKPMVPAFAVMGLVAIALYIFPGGWLLTPLILMQPELARTESPGVVETLRRCFAYSRGQRLPMIGTVLLGGLLAMLSVFLCCVPVIPALGFLQLLMAGLALALSSGAEEA
>NZ_CP017172.1|WP_140786789.1|405748_406420_-|DsbA-family-protein
MKTLHKPLQITVYQDVLCSWCYLADLRLDVLRQEMGEAVRWSVRPYPLRVHDVLPTTREQRALVEEVERAQREPDAAARMLSTDLWLGGDPPRTSVPALAALEAARLQGPQARAFLARAMQRAALEQGVNVSRPDVVFELASRVGLAMNEFSAAFRSEETRRLILDEHRDATHRGVRGVPTLVIGGRWMLCGLRELAEYREHILACLGKVSVPRSGSPERVVH
>NZ_CP017172.1|WP_140786790.1|406585_407575_-|RimK-family-alpha-L-glutamate-ligase
MSPRKVKPKKVPVPPGSQAPDRPERAPRRGHAKKTVVILSRKRALYSTRRLVAAIRARGHRPLVLDTLRCCLLLAQDAPRMTYRGVEVRGVDVVVPRIGASITAYGLAVVNHFEMMGVPVLNPPTSIARSRDKLRALQFLSRSGLDIPRTVMAHDRSNVRRLVEEVNGLPVIIKLIKGTQGVGVMIAHTLSEVQTILDTFWDLGQEIVLQEFVAESEGRDVRALVVGDRVVGAMRRKAKSGEFRSNIHRGGEGQAIELTEPYMEAAVRAARVVGLEVAGVDMLEGHAGPRLMEINSSPGFEGLERATHMDIAGAIIDHALKYAEAKRAG
>NZ_CP017172.1|WP_174258605.1|407653_409084_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MSAPPLHPDDIHTSPGDVGQDLNHSPLLGETLVVDPRTTVKLHKCRLAVTSGPDTGRSVVSDKERLRCGAHPGNDLVLVEDRTASRHHFEIQFTERGYLLVDLGSTNGTFLDGRRIERAYLSPGSQIRAGSSVLTFAPLDEEVTIEPDREGELCDMVGQSVKMRQIFGLIKKIAPMGVSVIIQGETGTGKELVARAIHELSGRTKGPMEVLDCGAIPPNLIESELFGHEKGAFTGAVSSRPGAFERAHGGTIFLDELGELRLDLQPKLLRVLENHEVRRVGGNDVIEVDCRVIAATNRDLMKEIQGGGFREDLYFRLSVITIQLPPLRQRRDDIPLILKRALADPEVVGKHGKKRFSAESLGLLMSYSWPGNVRELMNVLSHVLTFSEGEEIQPAHLPPRVRGQVREGPLPFNEHLSFKDAKEQLLENFEREYITSVLTRCEGNLSRAARESGLHRKSIERLVKKYQLDTKGMKSR
>NZ_CP017172.1|WP_140796302.1|409285_410023_+|pilus-assembly-protein
MVEAALSLPLVVFLVLGTLQLFLMLQARVLAQYAAFRATRAGSVAHGECERMSHAAILALLPSFHSFIGMRTPEVGGEHGGGVGAPERLAMAFAPRRDNRYQAGLDGVHTGSIVWINRGLAGGGVESPQDRGFDDPGHLRRLEVRLIYWYPMRIPFANWVMSRMFLAQLGIQDYTAANPLVLAERNANWGAGEFTSTYALAADVRDELASRVGRREYVFPIETSFTMRMMTPVKARHFASMDCPR
>NZ_CP017172.1|WP_174259169.1|410019_411663_+|Tad-domain-containing-protein
MNRSHSRGQTMVLFALGTLLMVLMVTLTLSFTMKVRERIEAQTVADAAAFSNAVATARTFNNIAVINRVQIAHAVAQAGAASLVSWASLYRAQLNAARGGYSDWEWPYQLNVITGCPCAWKSASCARRCRCGSKGLRDLGNLQRKLRMEDQRVNAVFQAYEPLFALQMRGHQLAQNALYLAQQQNYQELKDAVDSQRFTNQILSNINPGANATDAAWQVPPIGGVNKDELTGGLACTQGGAVCDVPATVQHAVNAAMGSRGFHFVTWRQDLDYVAHLANLAWVINPPDMVLVEVATQGTTHFGKKGRQMPMIMPFAPAITAEDEGSILYLYNHMANGGGAPCPAAVGGTEGVEASLVSSGGAMPTPEHRWTGGSDPSPYMRHMLMPCMNPVSSCPGIWPLFLDYNLTQLLDGGDNNYGQPKNFAVVQRNLRTRELDPWDYSFRYRFERGSTGTQFDNRSFQMADGTANDVQTAMATGIAYFHRGHSVAFHHWSEPPNLLNPFWRATLVAADTDESGLDDAANTLDLSAPAAARTLRALRSVGYRGIQ
>NZ_CP017172.1|WP_140796304.1|411662_412682_+|pilus-assembly-protein
MKKTLRSRHARGQSLVEAALGVTLFVTIVTFGIHFAEVGFLSLKVQEAAISALWDGTHGQMHHIPVNYDPAGSSMRDAANDAQARYADFNGLSSTTGAGITQALTTGSNMAVDCEMGVGVDWGGTAVTRATYRDNGGTACRASATLAAWRFPRSFLDQGEAGLYKKRNMEDSLASLQVCAVGRPVGGRCTGSYSMLIDDWGLAGQLEAATCNIIMQDQLLPCTNAPYHAAVFSIYTPTVLAIPGAASMLAEQTLFWNPLPPTALAMVGLGMKERTMWISAAGEDVINFNQFPTLMDPINMGVWGTSPGSALGGITTLPYAAAHLQRFSKGACFLGKDCD
>NZ_CP017172.1|WP_140786791.1|412683_413007_+|hypothetical-protein
MIRFSGWIQLALVSAVLSSPAALAGRTECEADCGGKAGSTLAECTSRCPNGGRDAACASRCTKKFQEQFAACSKRCPPRDNIESPRKTGSRPQPQEFDVPAEDAVVE
>NZ_CP017172.1|WP_140786792.1|413049_413739_+|hypothetical-protein
MKQVLQGLLAGVLVLVAMEARAQRLPFTWDVPKVVAVVDVPGTVMAEGVPVRMSAVLSAEKPEVIGQHLVSRFQAWELHVPKPSLQPQLLRETMITALDTKQFISYTAILQANPDGTTTVFMGEANLAQGRQQPQSSVAPVFPGAADSMKAETESARTLTYSVNAKQAEVEAFYRTELGNAGFREEEPRLFRSPNEEIKLSFSPTKEGRLAVVVVRRTVAQEPASPTAD
>NZ_CP017172.1|WP_140873038.1|413774_416675_+|isoleucine--tRNA-ligase
MSDTPPKDKDFKDSVNLPRTDFPMKGNLAQLEPRMLGWWAERGIWGKILEQNADAEPFVLPDGPPYANGHLHAGHALNKVLKDIVVKYRNMSGRRCDFIPGWDTHGLPIEQAVEKRLKDKKIDKRTLARDAFLEACRAYALEFVDIQRAEFQRLGVFGSWEQPYKTLDFTYEAQEIRELAAFAKRGMLYRRKKPVYWCLYDQTALAEAEVEYENHTSPSVYVAFQAGAELAERVPSLKGKDVAFVIWTTTPWTLPSNLAVSVNPEFEYVFYQLGARVICVARELLPKVLAEVKADELAVKHVELPGGEVSAAALVDPSRILAYARGEELEHLTYQHPFYERRGRVILGEHVTLDAGTGLVHTAPGHGQEDYEVGLQYGLDIYNPVRPDGRYDDTVGPALEGRRVFEANPVVIQLLVEKGALLNGATDTVAHTYPHCWRCRNPVILSATYQWFIPMDAPFHGTQTFRQVVLEQVDKVQWVPSWGHSRIRGMLETRPDWTISRQRTWGVPICIAYCEGCEEAVVSPELMERVAAAVEKEGVGVWYRTPVKDFLGADFQCPRCGKGEFRRETDILDVWFDSACMFSAVLEKRQRIPADLFLEGSDQHRGWFHSSMLVAVGTRDMSPYKACLTHGFVVDGQGEKMSKSRGNVVAPDKVIQQYGAEVLRLWVAASDYRNDVRLSDQILKGLSEGYRKIRNTIRYALSNLYDFDPAKHAVPEAELLPLDRWALGRLAEVVARVRKAYEDYEFHLVYATVVDFVAGDLSAVYFDILKDRLYTWRADGQPRRGAQTVLYEVASVLLRLLAPVMSFTAEEAWQTLPGKPAESVFLGGFPVVSAKLDPALAERYAKLFAVRGAVQGVLEAARRDKRIGSSLEARVVLTAEGAARDFLQANQAELPGLFITSQVELGDVKGAAAQTLEVAQAFGEGVRVTAEVLPAHGEKCPRCWTYSDAVGQGGDVCLKCREALAA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_3

1043933-1044033

Orphan

Consensus_repeat	Method
GAGTCACCGACACGGACTCCGTGCCCGTCGCCGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_3

>merge|NZ_CP017172|3|1043933-1044033|CRISPRCasFinder
GAGTCACCGACACGGACTCCGTGCCCGTCGCCGCCGCGCCGTGTCCGCTCGTCGCCAAGGCTTCCGGAGTCACTGACACGGACTCCGTGCCCGTCGCCGCC

>NZ_CP017172|3|3|1043933-1044033|CRISPRCasFinder
GAGTCACCGACACGGACTCCGTGCCCGTCGCCGCC	GCGCCGTGTCCGCTCGTCGCCAAGGCTTCCG
GAGTCACTGACACGGACTCCGTGCCCGTCGCCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140873290.1\|1056480_1057938_+\|phytoene-desaturase	unknown	unknown	gnl\|CDD\|274273
NZ_CP017172.1\|WP_140787604.1\|1031994_1032663_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368175
NZ_CP017172.1\|WP_174259192.1\|1037646_1042149_+\|lamin-tail-domain-containing-protein	unknown	unknown	gnl\|CDD\|275366
NZ_CP017172.1\|WP_140797273.1\|1032789_1034304_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017172.1\|WP_140873282.1\|1044745_1049146_+\|chromosome-condensation-regulator-RCC1	unknown	unknown	gnl\|CDD\|227511
NZ_CP017172.1\|WP_140873284.1\|1050091_1051177_-\|esterase-family-protein	unknown	unknown	gnl\|CDD\|225256
NZ_CP017172.1\|WP_140873292.1\|1057934_1058861_+\|carotenoid-1,2-hydratase	unknown	unknown	unknown
NZ_CP017172.1\|WP_140797274.1\|1035068_1036493_+\|hydrolase	unknown	unknown	gnl\|CDD\|366286
NZ_CP017172.1\|WP_140787640.1\|1049350_1049950_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140787602.1\|1030780_1031989_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140797282.1\|1055409_1056420_+\|squalene/phytoene-synthase-family-protein	unknown	unknown	gnl\|CDD\|173831
NZ_CP017172.1\|WP_140853094.1\|1053859_1055413_+\|phytoene-desaturase	unknown	unknown	gnl\|CDD\|274273
NZ_CP017172.1\|WP_174258647.1\|1052088_1052652_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239264
NZ_CP017172.1\|WP_140787648.1\|1052766_1053852_+\|polyprenyl-synthetase-family-protein	unknown	unknown	gnl\|CDD\|173833
NZ_CP017172.1\|WP_140787608.1\|1034347_1034884_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238017
NZ_CP017172.1\|WP_174259191.1\|1036500_1037352_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140787601.1\|1030144_1030585_-\|host-attachment-protein	unknown	unknown	gnl\|CDD\|370820
NZ_CP017172.1\|WP_140873278.1\|1042307_1042970_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP017172.1\|WP_140873286.1\|1051186_1052092_-\|TIGR01777-family-protein	unknown	unknown	gnl\|CDD\|187553
NZ_CP017172.1\|WP_140873274.1\|1028151_1030047_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223910

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140873290.1\|1056480_1057938_+\|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].	3.72292e-81
NZ_CP017172.1\|WP_140787604.1\|1031994_1032663_+\|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.	0.00247501
NZ_CP017172.1\|WP_174259192.1\|1037646_1042149_+\|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.	4.28195e-24
NZ_CP017172.1\|WP_140797273.1\|1032789_1034304_+\|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.	2.95004e-101
NZ_CP017172.1\|WP_140873282.1\|1044745_1049146_+\|chromosome-condensation-regulator-RCC1	gnl\|CDD\|227511	COG5184, ATS1, Alpha-tubulin suppressor and related RCC1 domain-containing proteins [Cell division and chromosome partitioning / Cytoskeleton].	1.04049e-52
NZ_CP017172.1\|WP_140873284.1\|1050091_1051177_-\|esterase-family-protein	gnl\|CDD\|225256	COG2382, Fes, Enterochelin esterase and related enzymes [Inorganic ion transport and metabolism].	5.08684e-32
NZ_CP017172.1\|WP_140797274.1\|1035068_1036493_+\|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.	7.0773e-21
NZ_CP017172.1\|WP_140853094.1\|1053859_1055413_+\|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_CP017172.1\|WP_140797282.1\|1055409_1056420_+\|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.	5.64056e-89
NZ_CP017172.1\|WP_174258647.1\|1052088_1052652_-\|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_CP017172.1\|WP_140787648.1\|1052766_1053852_+\|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_CP017172.1\|WP_140787608.1\|1034347_1034884_-\|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).	5.64512e-05
NZ_CP017172.1\|WP_140787601.1\|1030144_1030585_-\|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_CP017172.1\|WP_140873278.1\|1042307_1042970_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	2.30279e-14
NZ_CP017172.1\|WP_140873286.1\|1051186_1052092_-\|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.	1.20629e-119
NZ_CP017172.1\|WP_140873274.1\|1028151_1030047_-\|HAMP-domain-containing-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	4.88941e-51

>NZ_CP017172.1|WP_140873278.1|1042307_1042970_-|TetR-family-transcriptional-regulator
MAREPAQRELKQERAARTRMDILEAAIHLFARRGFLATTMADLSRAIRMTPGALYWHFPTKEDLLLAAIEELHQRCLRAFQLPGDDRELPAREQFQAICERTHLLLREHREYGIFFAMLAAEAADSNDQVAEAIRDKLALYATTLERLIRHGQQMGEFRQDVDALAAAHSLLGGLLGMLVHQNLFRASVDYDPLYRAVMLIHQAGLVQATGFDCVNASQS
>NZ_CP017172.1|WP_174259192.1|1037646_1042149_+|lamin-tail-domain-containing-protein
MRMSPRLLLAALGAVLLFHAGCGDEPGCEGASCNPQAVCGNNVVEQGEQCDDGNKVDGDGCESNCTPTPAPGAVCGNGKLEGEEVCDDGNTVDGDGCQANCTPTLTQCPAANAPALPDGATCAVTQPGSAARLFTGVVLKDGETLVGGQVLVDAQGVIQCAACDCSAAAGAAEATQVSCPGGVISPGLVNPHEHITYPMEPYVGSEERYEHRHEWRTGRNGHTRINSPAASAADNVRWGELRQMMAGATSMAGAGGQAGLLRNVDVNNTALQEGLGEGVVNSDTFPLGDTSGNLIASGCGYGSMPTTNSLPRSAAYLPHISEGISTAALNEFLCLSTGQNNVMQPRTAVIHGIGLTAKEIRVMAENGTGLIWSPRSNISLYGDTAMVTAYKNQGVTIALGTDWLRSGSMNLLRELQCADYLNTSHYARTFSDEDLWRMVTSNASDLVDTFEKTGRIAEGKVADLAIFQLRTFAHSPHRAVVTANPEHVVLTMRGGKALYGDQALMAGLRGADTCDTLDVCGASKEVCLQSEIGKNLAALTSGATAKYPLFACGTPENEPTCSPRRASLDSRWPAVVNNSTSYTGEVRAADKDGDGLVDSVDNCPAIFNPIRPMDNGKQADSDGDGIGDACDPCPLEAGNACTSFTVGDDDHDGIVTWLDNCPFVANPDQADADGDGKGDACDACSSVPNPGDLGCPATIHELKTPVGGSLPLVGKPVSIMDVVVTGVVKGGASSQGYWVQTYPLPSGASVDNSGLYVFSPKGDLAVGDRIDITTGVLLLYFGLPELTEVKYVKRSSGNEVPAPVVVTTADIRTGGPRAAALEGVLVEVRDVAVNTGVDEFGQFLVNEAGDAGQPGLMIDDQAYAFPVPSIGTRFGALRGVLTYNFNDSKLVPRFQADMPLPPPSLTGFGPNGYARVGGTGPVNTFPQTLTLTLSSAYAEALDVVITSSDESALSVQGGRITIPAGQTSATVQVNAVAPAQSVTLTATLGGSTQTATVRVLGADEQPEVVGVTPGDVTMVPGGEVVFTVRLDRPAPANATVALSVNPATGFGTFVPANGTLTVTENATEAVFSFITEAAATATEPGTVTASIGASSASATVTLDQNAPRLTALSPSSAVTIPAGGTQTFTLTVDRPAAQDTVVELAVVPGAGVQNYGTVPASATIPAGATEVTFTFTADAQGEGTGTVYATLYGITQTTELTVLPPPPALSAVTPAVATVYFGTQQVFTVALDRRAPAGGITVDVALEPATGMGELSSSTVSIAEGQTTGTVTFTAGEEDAQGRLIASYAGVTRGVDITIAERPAVGHIVISEISARGATAQNDEFIELYNPTGADITLNGWKVQYKSAASTTNYSGSVDIPDGTVIKAYGYLLLAHNSGYTGTVTKDVGYAFDMSASTSGGGHVRIGPNLAADNLNDPNTVDKVGYGTANQPEGSAAPAHPGAGGSLERKARPNSTAETMAVGGADALAGNGHDTDDNGSDFIVRAASQPQNSQSPAERP
>NZ_CP017172.1|WP_174259191.1|1036500_1037352_-|hypothetical-protein
MDVAVLTFEGLPQLDAFDASLLPALAALGVEARPVVWDDPAMDWKTVRLALVRNTWDSHLRRDAFVAWADKVGRLTQLHNPAPVLRWNTHKHYLRELEEKGVLVTPTTWVRKGDTLDVGELAFRHGWDAVVLKPAVSAGALKTHIFPRAEAHVATARLAEMTREGDVMVQPYLTAFETEGERSYVFFDGVLSHAVRRPPTLLDAPRGFSEPTAFTPEDAAELRLAESVLEAVGRPLLYARVDVATDNAGQARLQELEATEPRLFLSLDAGAAGRLARAIVAKL
>NZ_CP017172.1|WP_140797274.1|1035068_1036493_+|hydrolase
MRRLLAAVFCAAAVLAACEDDSPPPPTPPPPSTETYPDAGTRPDAGTQEPWACQRSTTVHNAPMRLLTRLQLEMSRATSSAQRTEAIDRFVAEVEEQGGRPLVSDVKAGRPRVAFFVRGEAGRDTFVAGDFNGWAATATPLVQVRDTDLYVAEVEVPRTGPQPYKLVKDGDFIADPGARNVAWDNFNRYDVGQFNSLIYPELQDAAKGRLTAWYDVPATVLGDVRDVFVYTPAAYDGRECPALPVMYLHDGNESLTRESFAESADTHYAARPEDSAVLVFVALPDQSVRLAQYTFPPARAPGWPTPRGDDYLAFLRDDLMPRVEASYRVKTGPRETGIAGASLGGLISVYAGFQMPEKFGFVGSQSGTLFWPHDGEVDRDDGNAMILRAGQEPVVPVRFYVDHGSPVAGCTRDGEEGGDDCQSNLQFVEALRGRGYGVAHWNEPGAEHDWAFWKRRLPKLLCNFRNEAPAVCGL
>NZ_CP017172.1|WP_140787608.1|1034347_1034884_-|FHA-domain-containing-protein
MARALLLSLLVRQHMALKEKFRAKYPHPWLVWEAGAWNVPEVVEGNVAATRLPLTDLRDCLPAGDALCFELVGHTDGSPLRLGRASNNALVVNDATVSREQLHLSPTLEGRWSVTRVAASRPVTLGGTALEPEQPTVLQPGAQLHVGDVRLTFHEAEDFNERIGRIAAQVLAQTAAPR
>NZ_CP017172.1|WP_140797273.1|1032789_1034304_+|protein-kinase
MGSDDAFMQTVQSRAEATVSDAGARASDELQEGSTLGNYQLEQFLGEGSMGRVFQARHTRLGRQVALKVLRPEHARDGGFVRRFFQEARTVNQINHEHIVEIFDFVDESATGGHVYCVMELLRGQSLSSLAQAEPLTLARIQRFVVQVCAALGAAHQVGVVHRDVKPDNLFVIHRAGQPDFVKVLDFGVAKLLTAEGGTTGTVDGTIIGTPAYMAPEQAAGLPVDARSDIYAVGNILYELISGKPPFQAPAFGHLVVQIITQPPPPLPSHLPSGEPVPPQLAELVMRCLSKEPEARPQSLAEVTTALLLLPASAQALTPAPAELALEASERPTHKVRVAVTGRWHRQAVVTVGTAALVVVAAVVTWSGMQPEPAPAAAPVAHAADVVARSVAEAPAAPAAALQLLPPVTLTVRSFPEGAQVLRLDTGELLGVTPLVKQVSGESAPLRLRVELAGYAPLERMVNLDKHAELEVPLVKALPSPRQKPAAGTQRATDKKSRARPVTQ
>NZ_CP017172.1|WP_140787604.1|1031994_1032663_+|hypothetical-protein
MKTFESRLRVWCGLLLVAGAVGCTVNFPDDVPYTCTETADCGGDGYVCTSLPDNGPRYCCLPDPAEVCNGLDDDCDGLVDNLETACYTGPEGTLDVGLCHAGESICTRDASIACVGEVLPGLETCNGLDDDCDGAVDEDFDLKTDPGHCGACNNDCSFLQDCVNGECVRRQELDCANGQDDDGDGFTDCQDRADCPTNTQCGPLRSADENDYPRCQVNGVCL
>NZ_CP017172.1|WP_140787602.1|1030780_1031989_+|hypothetical-protein
MRIPVVPVTALLALALLAAPSWAQEQGGLGLDLTSDAPAEQQGMDIGLDLRPSNPNADLLPRFALVGLYATERAGAQQASSWVEALARGALSSAMVAQASDLVETRERLAEGHDAAVRCAEAACFAEPAELLDADLLTTARLSLEDAGWTLRTWTYDRDSRVVHEDFVTGRNPRDEDFVNEAAAMLSKRLTALARPRAMLTVNVNVPQAVVKVGERIVGVGSVEVRQAPGPVVLEVSADEYGTHARTLDLKPGARETVDVMLEISGPAPDGPPDDSVAGVASSRKAPRKSLFKRPALYTALLGLAAVGAGVVMGMAAKDVEKRGGDADGDGVFDVTRKERLDAQSQANLATALLVGGGAVTAGSVAWLVVVPARSAPASTSVAPGSSGGASTSLHLMVGGSF
>NZ_CP017172.1|WP_140787601.1|1030144_1030585_-|host-attachment-protein
MANGTLWILVGNASRARLFATDAKAEEDWRLVEEFHHDESRARQAELIEQADNPNAGTLHGPPAENEPNGRRELEHDRFARELSVFLDKAHDRHDFDKLVIAAPPGFLGRIRRSLSARVRQRVLLDVDSDYSNVPAKELPNRVPVI
>NZ_CP017172.1|WP_140873274.1|1028151_1030047_-|HAMP-domain-containing-protein
MALSLPGTKSLRGRLTFYATLLSVVPLLTLTWLQARSARQVMEEQIHASLLSEAEGVKDLLESTLAEREASARGWAEDPAVRAALRGDVSPADAMLGVLQSRYLTLNGIVVFDDTGRAISANTPALRDEYLRRQDEVRRSPWFAEAQQGRTSSEGITEEHPIFTGHVLSLAFPVLDPVSKHRMGVLLAAFDWAHVDQLVQPALARAHQRALKSFAITLQRPDGTPMYDSRGANAQGNDALLAVTAVNGTDVRDVADGWHFVARVDPAEAYAPVVRVSRVALLMAVGFIVLAVVGAWLLSHRISGPVLALRAAVTRLVSEGDLTQTLDVKAGNDEVGELAGAFGLLVFQLRETAQSLHTGTRVLSETVAELQTASTQQERNVARQAAALQQTQVTAQEIKQTSMLASEKAEDVLKRASMAEEVGRAGEGAIRDSLGGFSEILSQAEQMTERIAQLNERTQQIGGITQTVKDLADQSNMLALNAAIESVRSGEHGKGFGVVAREIRSLADQSIQATDRVREILGDLSSAILSTAKMTEQGYTHMESGLEQVRGTGERLKELAAIIQDNATAVRQIAGAVSQQNAGIAQIFSAVTDLSSMMNDTQESLAATTRAAKLLQDVSEQMQDVARAYRI
>NZ_CP017172.1|WP_140873282.1|1044745_1049146_+|chromosome-condensation-regulator-RCC1
MHHLIEETPMPPDMMAGTRRLLMCLLSALLMAGCEPSGELAMPETPHATRTQRVVVTAPPMRIAAGSQHSLYLSPGGDVWAWGGNGSGQLGGAETSLLGLAPVRLAALEDIVSVVSGEAHSLALGADGTVWTWGGNSSGQLGDGSTTDRATPMRVAGLDNVVAVAAGDFHSLALREDGTVWAWGTNFHGQLGRGHTQPGLTPERVPGLNGVVALAAGFDFTLAVLEDGTVRAWGSNGSGQLGDGTFTQRLSPVKVSQLSGITAVTAGTYHALALGKDGGVWAWGSNASGQLGDGTWNDRAVPRQVPGLERVKAVASMDSDSLALLEAGAVFAWGANGSGQLGDGDTTDRATPGPVPGLKAVASVVGGAQHALALRKDGTLWAWGGGLSGQLGHGGSERHVVPAPVMRLAGVTSMATGSFHSLAALGDGSVWAWGRNTSGQLGDGSTAERHAAVRVEGLGGVRSVASAAHHSLAVGMDGTVWAWGRNAAGQLGDGTTTDRARPVAVPGLTSVTAVAAGGSHVLALRSDGSVWAWGYNALGQLGDGTTVDRLTPVRVSGLGAVVAVAAGSYFSMALQSDGTVWTWGEGFEGQLGDGGGVQRLSPVRVEGLANVTRVAAGSAHALAVRGDGTVWAWGDNGEGQLGDGSWADRFRPVQVPGLQGITAVSGGRSHSMALQGDGTVRAWGYNGYGQLGDGTLTSRVRPALIPGLTGIQALHPSHLHVLALHADGTLRGWGYNRFGQLGLGAAGWSALPVQVRGIGRVDRLSVGRAHTLMVRADGTVMAWGENGSGQLGDGTSTHRAGPVSVRGVPCVRSVASGLRHSLALACDGTVWAWGANGRGQLGDGTATPRVTPGLVEGLRGVVALAAGGDASVALRADGSVWSWGGNASGQLGDGTTTDRALPAHLEHLSNVVAVAVGETHALAVGEDGALWAWGANGSGQLGDGGTEPSLTPVRVKGLERVASVAAGRAFSVAVRDDGTAWAWGANPSGQLGDGTNLARSVPKQVASVKGIRAMSAGAHHVVALSADGTVWTWGDNTLGQLGDGSSSPTWMYPRQVPELRGVEAVAAGEQFTVAVLLDGTARAWGSNEYGQLGDGKTGPQLTPMAVKIDGPKIRPPVRAVRAWGQHAVVQMSDGTVQAWGDNAFGQLGDGTTTRRAVPLEVRGLASVVAVSSGAWHSLALRSDGTVWAWGANGFGQLGDGTSTSRTRPVQVAGLGDVVAIGSGGYHALAVRSDGSVWTWGYNAFGQLGDGTAESRSLPIRVEGLEGVVAVAGGDHYSLALHSDGTLSAWGNNASGQLGDGTGTTRYSRVGVKGVDGVVDVRAGAAHTVALRGDGTVWTWGDNAFGQLGDGTSGTRMRLVPRPVPSLSSVSAVGAGARHAFAVGLKGTVWTWGRNSHGQLGLGDNANRTEPLRVRELTDVTVVSGGADFSLAMKRDGTVLSWGSSLYGTLGLGAAGQRSSPGQVALP
>NZ_CP017172.1|WP_140787640.1|1049350_1049950_-|hypothetical-protein
MSRIDGGNRPSSPKGPVHERASAPEQRPASGTATQGTKGVQAHRTVQTFQGRSDFEPDRRPAQRGVTAPPPPPDATAIAGADAELELLSEFPDQADAQGGLASAMLHAHANEPASQARIVERLKQDGRLESLFGEVFREGNPYVEQPHRNAVVRALGTAMARGTVTSDDLRAFARGAYAQEWRQIGSELTTPRPLTEKP
>NZ_CP017172.1|WP_140873284.1|1050091_1051177_-|esterase-family-protein
MDAKTLEARARAEGTPVIDSDTATFVWRGRGPICLQGDFQDWRGKPLPLKRVAPGLWARTLTLPADAYVEYALEDPRGRRVEDPLNRHPSDNGFGGINHSFHMPQARSSLPARHPRGAPRGRVTRHVVDTGDVDLPGQRRVYLYAPPTDTPVPLVVVYDGEDYLRRVRLPELVDTLMAEGRMRPVALALVCNGGETRSMEYACSEYTVGLLKWKVLPLARQKLSLVDERRSPGAHAVLGASLGGLMALYTGLRMPDVFGRVLSQSGAFAVEGHDFVVFDLARPPPRRPLDVWLDCGRFEGLLEGNRRIVPVLSEAGHQVELREYSGGHNYPAWREDLVHGLERHFPPPPAKRRESLRFSGR
>NZ_CP017172.1|WP_140873286.1|1051186_1052092_-|TIGR01777-family-protein
MKVALTGASGFLGPGLVQGLLERGHQVHILSRNVEHALARLPAGVTGAPFDAGSPLPPEALADAEAVVHLAGEPVAQRWTREGKHRIHDSRVLGTRAVVAAMRGAGTVRRFVSASAIGYYGGTRGADPLTEESPPGDDFLARVCVDWEAEAMQARESGIATAVVRMGVVLHPDGGALHKMLPPFRVGAGGPVGSGEQFVSWVHRDDARDLLLFLLAHPQVEGMVNATAPTPVTNAFFAHTLGHVLGRPSMVRMPAFMLKAALGEMAKVVLEGQRVLPQRAHEAGFVFRYPELEGALRDLLA
>NZ_CP017172.1|WP_174258647.1|1052088_1052652_-|hypothetical-protein
MKAWIAGALSISLAAGSALGAAPATEPVDATLRTSAGKEVQLSKWRGKPVILFYEDKDSTKLNSTLKKELFARGQERGILDAAWVLAVANLQNFDFFPARQIALSFVRDEEKKVGVPILVDMDGALGKAPWKLPVKTSNIVLLDSEGALVYRHSGRMKPDELTTFFAVLSRLVGVDLNAPAPSEPSP
>NZ_CP017172.1|WP_140787648.1|1052766_1053852_+|polyprenyl-synthetase-family-protein
MALTLPDAQPPTGLLPLEQAWLQLVQAEVETSLAELFELPDEAGLDVRWTQALTQARAYALRPAKRLRPALVMAGHCLARGSAVVPSGLWRFAAGLELLHTFLLIHDDVADQAELRRGAASLHRLLAPGRAGEDLAVVVGDHLFARALEAMLGSGLTGVAGVVQYYLGVCRHTAAGQYLDLDLGRAPLAEVTLFQTLRVAHLKTARYGFCAPLVCGAMLGGASSGLVEGLERVGRHVGLAYQLRDDLLGLFGDSNVAGKAADGDFLQGKRTFPVLAAFARATEAERMELEALWSLPVEQKDAAALARARALVESCGGRAACERMVVRASRAARRSLQSLPNPNGVRELLDALIARLAHRAA
>NZ_CP017172.1|WP_140853094.1|1053859_1055413_+|phytoene-desaturase
MSASTQGRRIVVVGAGVGGLAAAARLAHQGFDVQVFEKTQGPGGRCNRLQVDGFTWDLGPTIVLMPEVFEETFRAVGRRIEDYLTLLKCDPNYRVHFRDGSDVTFTSELCAMGRELERVEPGSYARYLAFLAQGRVQYRTSLDHLVGRNYAGLRDYLSPRVLARIFQVRAHRRMYGDVSRFFQDERLRAAMTFQTMYLGVSPYASPAVYGLLPFSELGVGIWFPKGGLYAIPQALERLAREEGVRFHYGAPVEQILTDGGRTRGVRLEGGEVVEADAVLCNADLPYAYEKLLDSKATTLKRKEKLRYTSSGYMLYLGMKRRYPELLHHNVVFGRDYKGSFDDIFERFRVPEDPSFYVNAPTRTDASLAPEGKDALYVLVPVPHQHPDLDWKVEGPRVRAKFFARMAELGFPSLESDIEVERVFTPDDWAGTFNLARGSAFGLSQNFTQIGPFRPSNQDARVKNLFFVGASTQPGTGLPTVLISARLVTERLMTWAHAQGVSLSPRTAAATPLEGVAA
>NZ_CP017172.1|WP_140797282.1|1055409_1056420_+|squalene/phytoene-synthase-family-protein
MSPPVDKALVERGYVLAKQVTRHHAKSFFFASYLLFGLRRKAAFALYAFCRRLDDMVDGDDAVSAADALPVRLARARQRVAELYLPMPELASRELGPPADRVKGSAAATPWDAREFAALEHTVRHFRIPEQPFQDLISGMEMDLTKHRYTTWAELDLYCYRVAGVVGLMLTPVLGCSDAAAVEPAADLGRAMQLTNILRDVREDLERGRVYLPAEELAAFGLSEDDLRRGQVDARWRSFMRFQVERSRAYYARAAAGVRYLTGFGSQRMVRLMGAIYGDILRDIEARDYDVFSARAHVTTRRKLALASAAMVRPAAVLPVPQGEVRMPLLPTGTGG
>NZ_CP017172.1|WP_140873290.1|1056480_1057938_+|phytoene-desaturase
MKRTRVAVVGGGIGGLTAAGLLAKEGHEVTLFERGTSLGGKAQAVTVNGITLDTGPTLLTLPHLVRGTFQQLGAEDLLPRFTELEPQCAYRFEDGCDFTAYKDVERMAESAAGVRPGERDGIRSFYTEAAAIWRAAGEPYLEAPFEGMAGFMTRVAKRGVGAVMAGMKMGTLHELAARHFKTDHLRQYVGRFATYTGASPYEASAAFALIPHIEHAYGVHHVRGGIGALVDALGQAVRRLGVRIHLDTRARFERTREGYQVGPQEGMERFDSVVVNADPLERLARAEEPLALSGFVLLLEVEGRIALPHHTVLFGGDYRREFDELFGGQLASDPTVYFCNPSATDESMVPPGRTGLFVMVNAPALPVDARGAEQATRDWEAGAERVRAQMLERLCRHYPALKGRVRVIGQRSPVDLAAQGAPGGSIYGFLPHGKFGPFRRPRIRGNTPGLFFAGGGTHPGGGVPLVMLSGRFAAELASQHLRRDA
>NZ_CP017172.1|WP_140873292.1|1057934_1058861_+|carotenoid-1,2-hydratase
MMRLAKLPALPDAAGTYRWFYADVTAGPYSAVCIFMLGSLFSPRYSVAARRGGRPLEHSAVNFALYHEGVRRLWVLSEYARAELEAPGRLRIGRSTLSYEGDGTVRMVVDDWTAPWGRPVRAGLTLEPMTPVGEVVQLMPGLPHYWQALAPRSQARLEVSSLGIEASGLGYHDTNHGGELLGARLSGWHWARTHREDETVVDYHLPEGVAPLRVVAGARGVRCERGPALVEARPTHITSWGLRVPSRLHAGNVVVGQPKLLESSPFYARLEARQGPLDSLGEVADFRRFHSPFIRWMAHFRTRMGRAA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_4

1157410-1157507

Orphan

Consensus_repeat	Method
CGGTGGTCATCGCGGTGGCGGTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_4

>merge|NZ_CP017172|4|1157410-1157507|CRISPRCasFinder
CGGTGGTCATCGCGGTGGCGGTGGTGACGGCGGGCGTGTGGGCCATCTGGGGACCCGAGCCTCGGTTGGCGCACGCGGTGGTCAACGCGGTGGCGGTG

>NZ_CP017172|4|4|1157410-1157507|CRISPRCasFinder
CGGTGGTCATCGCGGTGGCGGTG	GTGACGGCGGGCGTGTGGGCCATCTGGGGACCCGAGCCTCGGTTGGCGCACG
CGGTGGTCAACGCGGTGGCGGTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140787793.1\|1165752_1167015_-\|TolC-family-protein	unknown	unknown	gnl\|CDD\|224455
NZ_CP017172.1\|WP_140787797.1\|1167528_1168374_-\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|225567
NZ_CP017172.1\|WP_140787780.1\|1154582_1155980_-\|chloride-channel-protein	unknown	unknown	gnl\|CDD\|238233
NZ_CP017172.1\|WP_140800615.1\|1152312_1153371_-\|methylamine-utilization-protein	unknown	unknown	gnl\|CDD\|188554
NZ_CP017172.1\|WP_140787787.1\|1160475_1161357_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140873361.1\|1144592_1147088_-\|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I	unknown	unknown	gnl\|CDD\|181856
NZ_CP017172.1\|WP_140797343.1\|1168494_1171695_-\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	unknown	unknown	gnl\|CDD\|226220
NZ_CP017172.1\|WP_140873367.1\|1150364_1151504_+\|di-heme-enzyme	unknown	unknown	gnl\|CDD\|188554
NZ_CP017172.1\|WP_140873369.1\|1153391_1154483_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP017172.1\|WP_140853124.1\|1142397_1143528_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	unknown	unknown	gnl\|CDD\|181076
NZ_CP017172.1\|WP_140873375.1\|1164556_1165756_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP017172.1\|WP_140873363.1\|1147674_1148289_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|224511
NZ_CP017172.1\|WP_140787795.1\|1167124_1167439_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259406.1\|1161417_1164540_-\|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|226220
NZ_CP017172.1\|WP_140787776.1\|1149431_1150352_+\|metallo-mystery-pair-system-four-Cys-motif-protein	unknown	unknown	gnl\|CDD\|188567
NZ_CP017172.1\|WP_140873359.1\|1143466_1144567_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|181320
NZ_CP017172.1\|WP_140787784.1\|1158730_1159144_+\|four-helix-bundle-copper-binding-protein	unknown	unknown	gnl\|CDD\|153434
NZ_CP017172.1\|WP_140787786.1\|1159232_1160324_+\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|226985
NZ_CP017172.1\|WP_174259197.1\|1171681_1173415_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP017172.1\|WP_174259196.1\|1148456_1149380_+\|GIY-YIG-nuclease-family-protein	unknown	unknown	gnl\|CDD\|198398

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140787793.1\|1165752_1167015_-\|TolC-family-protein	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	4.51512e-29
NZ_CP017172.1\|WP_140787797.1\|1167528_1168374_-\|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_CP017172.1\|WP_140787780.1\|1154582_1155980_-\|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.	5.4731e-47
NZ_CP017172.1\|WP_140800615.1\|1152312_1153371_-\|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.	3.51823e-84
NZ_CP017172.1\|WP_140873361.1\|1144592_1147088_-\|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I	gnl\|CDD\|181856	PRK09436, thrA, bifunctional aspartokinase I/homoserine dehydrogenase I; Provisional.	0
NZ_CP017172.1\|WP_140797343.1\|1168494_1171695_-\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP017172.1\|WP_140873367.1\|1150364_1151504_+\|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_CP017172.1\|WP_140873369.1\|1153391_1154483_-\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	5.38346e-07
NZ_CP017172.1\|WP_140853124.1\|1142397_1143528_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	gnl\|CDD\|181076	PRK07671, PRK07671, bifunctional cystathionine gamma-lyase/homocysteine desulfhydrase.	5.39198e-168
NZ_CP017172.1\|WP_140873375.1\|1164556_1165756_-\|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.	2.27821e-53
NZ_CP017172.1\|WP_140873363.1\|1147674_1148289_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	4.11178e-21
NZ_CP017172.1\|WP_174259406.1\|1161417_1164540_-\|efflux-RND-transporter-permease-subunit	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP017172.1\|WP_140787776.1\|1149431_1150352_+\|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_CP017172.1\|WP_140873359.1\|1143466_1144567_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|181320	PRK08247, PRK08247, methionine biosynthesis PLP-dependent protein.	0
NZ_CP017172.1\|WP_140787784.1\|1158730_1159144_+\|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_CP017172.1\|WP_140787786.1\|1159232_1160324_+\|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_CP017172.1\|WP_174259197.1\|1171681_1173415_-\|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.	2.35887e-98
NZ_CP017172.1\|WP_174259196.1\|1148456_1149380_+\|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.	8.95804e-46

>NZ_CP017172.1|WP_140787780.1|1154582_1155980_-|chloride-channel-protein
MAGRREPLDEEQSALHDSWDTVLRTVGRVVLGTVLIWGVCSALRYGVHATSDTLLAFASGRSLWWAPLVLAGVLLLGGLLRGLLNRRPGWSDVASDGVNVALFNYHITYEDPADDPRPRYSRPAIRLALRKAVATLLTLGTGASGGLEGPVVLVGESLGAGVARLTRARSEHTLRTCQLAGIAAAVGTLLNAPFAAALFALEVVYGNRIVYRKLAYCLLAGIIAYALNNRLLGFKPIFVAPPHPHTYTLGEYGLTALVAVAVSAPIALLFGLTMKHTRQVVERVSPVLRGAMGALCTVLVAGGLYYGAGMDFRHVLGMGEYTIAQLLADTPGPLSLWWYLLLIVGGKLLTTGFTVQSGGSAGMLIPSMVLGGVSGAATAQMLASVTGTGPADVTVFVVVGIASALVAVVGVPLAAIALVLEVFGSAYGPPAVLACCVTYVLTLRLSVYNEQRRVQAVATEPVASD
>NZ_CP017172.1|WP_140873369.1|1153391_1154483_-|hypothetical-protein
MKKHASLSSLPDLGRMLALAAMALLALPACGDDGATDEQLQASEDQRRQLEQQVSELEEEVTRLEAQVARQQLDAEAAQAELADITQQLEEARELLASQDWEGVYQQLTQVRAELAALRTQRAAMDGSLELNAAFVFGTAPFALGQTYATAGGDTVTFSQVRYWLSNVTLLKQDGTTRALTDSYHLMEVINAQELDGTSNPVTLPANRRERVQARAVPAGTYSGIRFSIGVDPTYNDDLSRQAGELHVLQNMASVSWMWFTSYIFTKTHGTYVTAQGTQGDFTWDTGTNANYRTVELPFPTTVTVNSQKHLAVNLQANVETLFTSLSPRTTPSIGATQSTESATLSDGFANMFSLVLVENADR
>NZ_CP017172.1|WP_140800615.1|1152312_1153371_-|methylamine-utilization-protein
MAAASLAWLLLGACGEGGPPPVEEGPFPRHLPVGMAVIPSPPDNPLTPEGIALGRWLFHSPRLSSNGQVSCATCHEQARAFADDAALTRRGVSGRPLVRHVPALINLAWMEGLFWDGGSKNLESLSLAPLTHPDEMGNSQLSSMMARLSSEPEFAQRFENAFGPDGLTLSNLLRALAQFQRTLVSADSRYDRWRRGEPGVSLSPQEQHGLALVQRHCATCHATELFTDNAYHNNGLDSDAAFGEGEAESRGRGRVTQRAEDAGRFKTPTLRNVAVTAPYMHDGRLATLEDVLEHYRGGMVPSTTLDAAFQRQGQAPGLSLDDTAKAAIISFLDALTDEGFLSERELATHNNP
>NZ_CP017172.1|WP_140873367.1|1150364_1151504_+|di-heme-enzyme
MVWRVGRRAGVLAVLAWLGAGCGGTDGEAESYVWKLPMGFPTPRVPADNPMTEEKVQLGRRLFFDVRLSRNETQSCASCHDPARAFTEPLVTSQGSTGETHRRNAQGLANVAYATSLTWANPSLTTLEAQALVPLFGKEPVELGFGDREEELLGRLRAVPELAAEFQRAFPEAVEPVSVATLTRALASFQRSLISGNSAYDRYVYGNEVEAMTRQQKRGMELFFSERLECDHCHTGFNFQDATVHEATSEPILPFHNTGLYNEDGQGAYPAEDPGLIELTGRPEDMGRFRAPSLRNVAVTGPYMHDGSLATLSDVLDHYAAGGHARLVSGGETSPLQSGFVRGFTLTEQEREDVLAFLESLTDTEFLTDPRFADPSTTP
>NZ_CP017172.1|WP_140787776.1|1149431_1150352_+|metallo-mystery-pair-system-four-Cys-motif-protein
MPRSPPVGIALRGDSIPRESAMVFAHRRAVRMLPFALLGVLGCGDDMEVAIPFEARVGSEPFACGRTYTGVGTTGTTYEPMDLRVYLHDVRLVTAEGTEVPLKLEQDARWQVEGTALLDFADKTGLCTNGTQATNLRITGTAPEGNYTGLRFKLGVPETQNHLDVSTAPSPLNDTSLYWGWRSGYLFTRIEGRTTGLPGGHVMHLGSTDCAPPPEGQTNGTAGCTFGNRPEVALDSFDLASGKVVLDLGALFSGSNLDENAAVPNTSVGCMSQQTDPDCAPVFSRMGLTHRSQEGAPGPQAFIKAE
>NZ_CP017172.1|WP_174259196.1|1148456_1149380_+|GIY-YIG-nuclease-family-protein
MRTVVSLHECKVRASLLLKELASTDASRAARAAERLRVLPGFAGLPLGEVLARKDSVQRKHALAVIAREQGHATWVDLKQVRELDFEHLLAHVGGAHLNRWFSSYAEAADSLRAQGGFLFPFREQFFVCEASLVEALGVDPADADWSCTGRDWMAPRDGAAQARLAQRFVRHSPSHASTSPDTRSPMSADSRRSELKRSYREAPPPMGVYAVRCLANGKVLVGASANVQGMLNRIRFELSTGMDRLPTLLEDWKRYGAERFTFEVLDVLKPSDEPVVAPEEELKVLEALWLDRLRPYGDAGYNVQGG
>NZ_CP017172.1|WP_140873363.1|1147674_1148289_+|sigma-70-family-RNA-polymerase-sigma-factor
MGKERGVTETGQLSDEVVRALVDNHRQFLAFLERRVGSRAIAEEILQAAFVRTLEKGGALKEGEGAVAWFYRLLRNALVDHYRRQAAEGRALEREAQEAEGATVDTELKQAVCACVGELVPTLKPEYADILRQVDLEERGVPDVARESGITANNAGVRLHRARQALKKQLERSCGSCAAHGCLDCSCKPSHRAGGALVSGSTDV
>NZ_CP017172.1|WP_140873361.1|1144592_1147088_-|bifunctional-aspartate-kinase/homoserine-dehydrogenase-I
MSSTSLQVMKFGGTSVGSPTRLRQVVELIGTHARQGPLAVVVSAMGDTTDWLLDAARLATEGDLEGALAVATRIADLAKANAAALAPGQATALAERVDGLLAPLRQLLQGVSLTRECSAPTRDRVLSFGELVSATLLAELLTAHGTSATFRDARQLLVTDDRFGAARVDLVRTRERLQAARETWGVEVPVLPGFIAATPDGRTTTLGRNGSDYTAALVAQGLGASEVTVWTDVLGLHTADPELVTDAYPVAHLTHGEGLELAAVGARMLHPRTMIPLIESGISLRIRNTMEPEHPGTLIDAIGSRDGQRPACIATREDLALLGIEVRKLSDQFQLGERVLAALREARVTVWMTAQSANGQSLAVVVPRPDAEHARSVLAAELALELSRREVEPLEVRQPVTLLTLVAEAMGHGVNVAGRFFSALGAVGVNVRASAQGASSRSLSCVVDAADTAIAARTTHAAFNLAHQQVSLFVLGRGTVGGQLLAQLRAQQALLRDRHGIALRVVGLADSKRALFDAAGLALDGVEARLEGVTPEAPQARTLVPLLDALRRLPVPILVDCTAAGGLEALYTEAFRRGIHVVAANKKPLALPWEAREALVDTARRNHVAYHYETTVASSLPVIDTLANLVRTGDTVRLITASLSGSLGFICNELTAGVPLSRAVRTARERGFTEPDPREDLSGTDVARKALILARELGLPLSLSDVALEPFVATDECASVDSFFQVLATQDAAYAERVARCRHAGTVLRYLARIDPSKAGTGSPVIRVGPVGVEAGHPAADLRGSESFVSFTTTRHSDFPLTVRGAGAGGAVTASGVLADILRISQTLRGR
>NZ_CP017172.1|WP_140873359.1|1143466_1144567_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MKLATALVHAGVRRDPSTGAVAVPIYQSATFQHPALGQSTGYDYSRTRNPTRSALEDALAQLEGGSRGLAFSSGMAALHCALQLFGPEDHVLLTEDLYGGTYRLVDRILHVPCTFVDTSRPSAVRDALRPNTRAIVVETPTNPMMRTADISELAAIARKAGVLLIVDNTFLTPWLQRPLELGADIVVHSATKYLAGHNDVVAGALVVKDAALGERLAYLQNGIGAILGPQDAYLVIRGLKTLALRMERHQANAREVAAWLRAHPGVERVFYPGVGGMLSFTVAHAALVPQVLASVQLCLFAESLGGVETLITYPTTQTHADIPAERREALGISDRLLRLSVGIEDSHDIIADLAHALRDSFAAHGA
>NZ_CP017172.1|WP_140853124.1|1142397_1143528_-|aminotransferase-class-V-fold-PLP-dependent-enzyme
MTSSPTWPTRFATRLLHTGHEQDPTTGAAAVPIYQVSMFDQPGLETPGEFDYARSGNPTRKALEGVLAALDEGHAAFAFGSGMAAVSSVLMLFSAGDHVVVTDDCYGGTYRVLTRVFSRFGLQATFVDTSDPDAVRAALRPNTRALLVESVSNPFLKRTDIPAMARVAQAHGALLIVDNTFLSPALSRPLTEGADIVIHSATKYLGGHSDVVAGAVVVKTPALAQELGFLQNAVGAVLGPQDCFLLQRGIKTLQVRLERQVRTAGALVKWLTGRPEVRQVFYPGTGAVVSFRLAQDTLAAPFVESLQLPLLGVSLGAVESIITVPARHSHASVPAAERERRGITDGLIRFSVGLEDLEDLQEDFVRAFTQAGRVAA
>NZ_CP017172.1|WP_140787784.1|1158730_1159144_+|four-helix-bundle-copper-binding-protein
MASVEVMNADSEMRQCIEDCLACHRVCLETLTYCLGKGGKHAEARHLRLLMDCAEICQTSANFMLRDSELHSRTCFACSEVCGRCAESCAQMGEDVVMKACADMCTQCSDSCWRMGGGVMSQTPNPEAAQRAADLPA
>NZ_CP017172.1|WP_140787786.1|1159232_1160324_+|Rieske-2Fe-2S-domain-containing-protein
MSSREEGRTSGTPAGHISVVHLPNAWFILCASSELGDKPLARTLQGSPLVLFRGEGGKPAALVDRCPHRNVPLSLGRVQEGQLQCGYHGWRFDGAGQCRAIPGFLGEPGARARCATAHATREQDGFVWVYSTPGVEPTTEPYRFPLLEAREYTTVRRTLRAPGSLHSTLENTLDVPHTAYLHGGLFRTEEKRNEIDVVVRRSADKVEAEYIGEPRPSGLVGRLLAPGGGVVQHFDRFLMPSIAQVEYRIGDTSHIMVTSAMTPVSDWDTLVYAVVTFRLPLPRWLVRAALPLIMPVALHIFGQDARILRQQTETIRRFGTEAYASTEIDVLGPGILRLLRAAEREKPGAVGDTVHETRLKMRT
>NZ_CP017172.1|WP_140787787.1|1160475_1161357_+|hypothetical-protein
MRFPVRAALAGAALLFAPQALATNYTLWIHGKNSGGTKPGNYADFSAWGPASTAAGVNKKAVNWDGRQRIGGQNERIRDALDCYCTGDNWCYIAVHSAGNLQIGYALALYGGSARYKKNATPNASGVCGNTDGKTQTGWNIKWVNVASGAAGGSELADMGEWAVDDPIVSDLKTTTARAMYNHNTTRGIRFNMYAGAKGKVYSGLLPGQDDDAVSYHSTGGVSGSAGGAYCNPSDWFCNDLTTGANACEGGQAKWTNHFVAFRDDAESHGHGANGKWEGIVGKVRADMVTNAK
>NZ_CP017172.1|WP_174259406.1|1161417_1164540_-|efflux-RND-transporter-permease-subunit
MNRILRSSFARPGLTVMLALALSAFGAVALQGLTRDVFPDLSAPIFNVIVQNPAMGAQELETAVAIPMEVALAGLPEVRRIRSTSQLGVTQLTVEFEPDADYFRSRQYVVERVAQAQSELPPGTDVPLVSSLTGRLNEVFEFTLEAEPGAAELMTLRDLAEFEVKNRLLAVPGVAGVERLGGYLRQFQVQLDPDQMVARGITLNQVEHALEGANLNASGGFVVQGPMEWTVRAVGRAESVEDLRDTVVAVRDSTPVLLGDVADIREAPAVRRGIAHRLKGEVVSCRVIKQFGADTQRVTAGIRVAIQELKQGLPPGVQLRIVYDQSVLVDSALGGVSRAILLGAVLVVLVLFLLLGDWRAALIVTLTLPLSLALAGVLLKFAGIGINTMTLGGLAIAVGLLVDAAIIVTENIVHGLREAKGQRSRREVALAASMEMARPIAFATLIVVSVFIPLFAMTGIEGRMYQPLAAAVVACLTASLGLALTLVPVASGLFLRTPREGQPEDVWVIRKIKHVYAPMLEACMRHAGLVRLVALAITVPALSLAFVVGSDFMPKLDEGALLLQTVLPPEASLEEVDRLNHLVEDALLKFPEVEDVVRRTGRAERTEDPMPHTLSDVLVILKPERGRSMEDLEAAMREAVGQVPGVSTLFTTPLGMRIDEGLGGSPADLSVRIFGPELETLAGLAERAQAIMSKVEGVEDLRAEKLTGLPQLRITVNRAAVARVGLTPGDVIHAVKVGMVGQEFAQVWKGQRRYDLLLRLADHRRGDATAIRGLLVDGHDGTRIPLSQLATIEETFGAGSIRREAGSRRIAVEASVAGRDLGSTAAEVRERLAAELKLPTGYFLDVGGKVESQQRAAQAMTVAIAVALLAVFILLYLALGSLAESLVIIATLPDAFVGGILALLIAGETWNVSSLVGLIGLFGIAVQNGLVLVAQTKLLMQHGKPFDEAIREASIGRVRPKLMTAGTAILGLLPLLVLPLHGTEVERPLAVVMVGGLVTSTLFTLLVLPTFYAFVHGWQVRVTQRLAARKAARTQTPGEH
>NZ_CP017172.1|WP_140873375.1|1164556_1165756_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MKPLHAAVAALFLLTACKRETPHDEQEHGHDEPPAQAGAHHDDHGVPHVRIASEMLRDLRITTAPVGVRPGGENVTVLGELTFSEDAYAEVASPIAARVSAVFVTTGQEVKQGEKLADLRSPELGKARASLQAAQAQAQAARQAAERKRTLADERIIARKDVQAAEAEATAAEASVAAARAELVALGVSEEELRGGNVPPGFVLRAPLSGTVVERTARMGQMADPNLPLFCIGDVSSLWLVVHAFERDAVRIQRGTQARITFAAFPGQEFMAKVGHVGQRVDATSRTIPVRLELDNADGQLRPGMSASAYIPLGDPGAPITAVPAAALQRLEGGWVAFLPTDARGVFERREVGRGRTLGGDVEVLTGLKPGEQVVVEGAFLLKAEAEKLSGGGSDGHAH
>NZ_CP017172.1|WP_140787793.1|1165752_1167015_-|TolC-family-protein
MPHPLTVAAFGLAATLLFPRVAAAQPGSADAALSLEETLALARQRAPALLEAAGRAAEAQGPVAAAASLLNDNPTFELQAGPRSDPGSPGHPAVRGVDLSVGISQSFELGGKRGARRESARAGLEMETARQRDAERRVLGDVAARFLQALHARERLSLAREAEAAARETANSAQRRFEAGDVPVVDVNVARVSLARMRAEVATAEGDEAVQLHQLRAMLGLPLTHPFAIRGELRVLALQPDTEAKTNTVAARPDITALEAELAQADADRRMGRASVWPDITAGFLYQREIDEIAYLGALSVPLPLFDRGDNARVTGEARVRRLQSLLAAARLEVDVQVEAARVQHRKRLEAVTLLEADALPLLSDNESLARRSYEAGEMGLAEFLLVRRDTLEARAAYLDSLLQAALARVQLAVETGALP
>NZ_CP017172.1|WP_140787795.1|1167124_1167439_-|hypothetical-protein
MLRIWLIVCLFLFAPGLGGLMPTLTGAVGEVCTQSCPDDDDQGQCAPDCIDCTCCSHVRSVAAHAPPPSFVLLVSRPLRVAYEKAEPLSADGGDILHVPIAPLA
>NZ_CP017172.1|WP_140787797.1|1167528_1168374_-|N-acetylmuramoyl-L-alanine-amidase
MSLRLPSLSSVFRATQAQAPRTAAAAAATVSAPPAGLRKGDSGPKVKQLQDALVKVGYMTKAQVTTGPGSFGPQTETAVKKFQADNKLPATGFYGDLTHAALKKALGTSGPTTPTTPGGKFTKPAVINAPSPNQNSRGGTKIDTIVMHHTATNNGAGDLSWMRNPQSKVSAHYMVDRDGKIYQLVGDDKRAWHAGKGELHGVPSDINNRSIGIEIVNDGSGKTPFTEAQYKSLTQLTGYLKQQHNIPMKNIVGHADVAVPKGRKNDPAPNFDWNRLRKGIS
>NZ_CP017172.1|WP_140797343.1|1168494_1171695_-|CusA/CzcA-family-heavy-metal-efflux-RND-transporter
MQPTEHGEQGFIGRIIGACARNPFLTILLVGALAAWAVHAVRNTKLDAIPDLSDTQVIVFTEWMGRGPDLVEDQITYPISSSLLSAPKVKAVRGQSMFGMSFIYVIFEDGTDMYWARSRVLEYMETARGRLPAGVTPMLGPDATGVGWVFQYALVDESGKHSLADLRSLQDWNVRYALSSVPGVAEVASVGGIVKQYQVQVDPNQLRAYGVTLGEVTRAVRESNEDVGGRVMEIAGHEHIIRGRGYIRSTQDIENIPLKVSEDGTPVLVRNVATVSLGPDIRRGVAELDGKGEVAGGIVVMRYGENALTVIEAVKERLEEVRAGLPEGVELVVTYDRSGLIEESISTLSRALVEEMLVVSLIIFLFLMHARSALVTIFTLPLAVLLAFIPMYYQGLTANIMSLGGIIVAIGAMVDASIIIVENIHKKLEAWEAEGRPGERREVIISAMQEVGPSIFGTLLVLTVAFLPVFTLEATEGRLFKPLAYTKTYSMGFAAVLAVTLTPALAVLFIRGRIRREDENPLNRWLVALYMPVVRFVVRHAKVVVALSVVAMAMTIPAFMRLGHEFMPPLNEGAILYMPTSPPGMSITEATRILQSMDGELKRIPEVVSVFGKAGRAETATDPAPLSMFETTVVLKPKSEWRKGLTWEALLAEMDETLQYPGMPNIFWMPIQTRTEMLATGIRSPLGIQVFGDNLDTLEQAAVAIEKAVAQVPGTRSAFADRSTGGFYVDIGVKREEAARLGLGVKDINEVVMGAIGGENVSQTVEGRERYPINVRYAREYRDSPELLKEVLVPTPAGAQVPLAQVADVRFVQGPPMIRSEGGKLVTYVFVDTARPIADYVKDAKAAVAREVKTPTGVRVEWSGQFKYFERATEKLKVVIPVTLLLVCLLLYFSTKSVVEMGIVLLAVPFSLIGAVWLLYLLDYNMSIAVWVGLIALAGLDAETGVVMLLYLTLAHKKADQEGRLRSMADLTETIVDGAARRIRPKLMTVMTDMIGLLPVLWSTGTGADVMKRIAAPLVGGLVTSFLLELTVYPAIFALWKRRHLPQEQPEEGTGEPPLPAETQTA
>NZ_CP017172.1|WP_174259197.1|1171681_1173415_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MSPPNRRRIAPWLGVLTLAVLAAVAWRPLAGWFFGTTSHTGTAPATHDAHGRAGTPLPDAALEYTRAAFEAYEGARALLAQDAVEGLAARAGELKAALQQAAEATQGDGTPLKAWLQQGADGASHLAAAKDAEAARQHFARVSEALIALAFADPRLQEDWHVFECPMVDGVNQWLQREPKLENPYMGRRMLACGTTSEWRSAAPAGAHGEGDIAHYTCPMHPSVKQHGPGACPICGMDLTPVSRAELESGIIRVDDLRRQRIGVKTAKVAQAPMDLSLRALGRVTFDEKSLVDVTLKLDGYIHELRVNATAEPVKKGDVLFTLYSPELYAAQQEYLLARQSQSAANASLVGAARKRLELWGLSAAQIERVAQRGQPVENMPFLAPASGYVMEKNVVEGAAVKAGERLFRIAPLAKVWVEADVYEQDLARVKPGQPVEVTLPYLPGKKYAGHVGYVYPSLQGATRTGRIRIELPNPELELKPDMYADVRFVLQGGARLQIPDSAVIYTGPRRLVFVDLGEGRLRPQEVKLGIRGEGTYEVLEGLSPGDVVVTSGNFLIAAESRIRSATDSFGGSHAAH

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_5

1398067-1398145

Orphan

Consensus_repeat	Method
CGGGGGCTGGCTTCACCAGCGCGCCGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_5

>merge|NZ_CP017172|5|1398067-1398145|CRISPRCasFinder
CGGGGGCTGGCTTCACCAGCGCGCCGCCTTGGCCTGCGTGCGGGGTGATTCGCGGGGGCTGGCTTCACCGGCGCGCCGC

>NZ_CP017172|5|5|1398067-1398145|CRISPRCasFinder
CGGGGGCTGGCTTCACCAGCGCGCCGC	CTTGGCCTGCGTGCGGGGTGATTCG
CGGGGGCTGGCTTCACCGGCGCGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140788094.1\|1388846_1390700_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017172.1\|WP_140788096.1\|1390815_1391406_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|225113
NZ_CP017172.1\|WP_140796359.1\|1395856_1396282_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|176862
NZ_CP017172.1\|WP_140788106.1\|1396368_1397952_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223959
NZ_CP017172.1\|WP_011551294.1\|1400298_1400712_-\|YjbQ-family-protein	unknown	unknown	gnl\|CDD\|376651
NZ_CP017172.1\|WP_140873479.1\|1404543_1405755_-\|lipase	unknown	unknown	unknown
NZ_CP017172.1\|WP_140853205.1\|1403307_1404540_+\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|272913
NZ_CP017172.1\|WP_174259409.1\|1398687_1400295_+\|L,D-transpeptidase-family-protein	unknown	unknown	gnl\|CDD\|341130
NZ_CP017172.1\|WP_140873476.1\|1401452_1402199_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|365914
NZ_CP017172.1\|WP_140788104.1\|1395523_1395850_-\|TerB-family-tellurite-resistance-protein	unknown	unknown	gnl\|CDD\|143581
NZ_CP017172.1\|WP_140788118.1\|1406004_1407900_+\|DUF4178-domain-containing-protein	unknown	unknown	gnl\|CDD\|379368
NZ_CP017172.1\|WP_090484863.1\|1394164_1395508_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP017172.1\|WP_020478251.1\|1407932_1408094_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140873474.1\|1384981_1388761_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP017172.1\|WP_140788100.1\|1392224_1392692_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP017172.1\|WP_140788098.1\|1391692_1391926_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237030
NZ_CP017172.1\|WP_140788102.1\|1392737_1394168_+\|MCP-four-helix-bundle-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_140873478.1\|1402388_1403354_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140788108.1\|1400715_1401450_-\|dienelactone-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223477
NZ_CP017172.1\|WP_140796361.1\|1405657_1406008_+\|adenosylmethionine-decarboxylase	unknown	unknown	gnl\|CDD\|376892

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140788094.1\|1388846_1390700_-\|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_CP017172.1\|WP_140788096.1\|1390815_1391406_-\|GAF-domain-containing-protein	gnl\|CDD\|225113	COG2203, FhlA, FOG: GAF domain [Signal transduction mechanisms].	2.58306e-10
NZ_CP017172.1\|WP_140796359.1\|1395856_1396282_-\|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_CP017172.1\|WP_140788106.1\|1396368_1397952_-\|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_CP017172.1\|WP_011551294.1\|1400298_1400712_-\|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_CP017172.1\|WP_140853205.1\|1403307_1404540_+\|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_CP017172.1\|WP_174259409.1\|1398687_1400295_+\|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.	2.48877e-30
NZ_CP017172.1\|WP_140873476.1\|1401452_1402199_-\|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.	4.24536e-65
NZ_CP017172.1\|WP_140788104.1\|1395523_1395850_-\|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.	1.58503e-05
NZ_CP017172.1\|WP_140788118.1\|1406004_1407900_+\|DUF4178-domain-containing-protein	gnl\|CDD\|379368	pfam13785, DUF4178, Domain of unknown function (DUF4178).	1.67035e-22
NZ_CP017172.1\|WP_090484863.1\|1394164_1395508_+\|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_CP017172.1\|WP_140873474.1\|1384981_1388761_-\|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.	2.06563e-10
NZ_CP017172.1\|WP_140788100.1\|1392224_1392692_+\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	0.00107892
NZ_CP017172.1\|WP_140788098.1\|1391692_1391926_-\|hypothetical-protein	gnl\|CDD\|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.54493e-08
NZ_CP017172.1\|WP_140788102.1\|1392737_1394168_+\|MCP-four-helix-bundle-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.03263e-38
NZ_CP017172.1\|WP_140788108.1\|1400715_1401450_-\|dienelactone-hydrolase-family-protein	gnl\|CDD\|223477	COG0400, COG0400, Predicted esterase [General function prediction only].	1.4196e-32
NZ_CP017172.1\|WP_140796361.1\|1405657_1406008_+\|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_CP017172.1|WP_140788106.1|1396368_1397952_-|SDR-family-NAD(P)-dependent-oxidoreductase
MKLAETAPTPAPEALPPPAPLSLDEVRRVTQLLEAISEDRFLLAGLPEEDRIAFLSAAGRVLHPDRDTKSRMAKALRRDRKKTKREHDRAIRATTEIRTLRRSAIFTVPALPPPPPSEAGPERILEQPRRCYVCKAEYRKLHFFYDAMCIECADYNYAKRTQRADLNGKVALITGARVKIGFQASLMLLRSGARVIATTRFPNDAAQRYVQEPDFADWAHRLHIHGLDLRHAPSVELFAKYIEQTHERLDILINNAAQTVRRPPGFYGHLLPGEMRRADDLPAAARALLAGHDACVSTVQPAALGAGKAGGSELATTWRSNDPALGIHSSAALSMLPYALEQEGDVRAIFPQGRLDADLQQVDLRDMNSWRLRLAEVQTAEMLEVHLINAVAPFILVGKLKPLMLRDRSSPGHVVNVSAMEGSFSRGTKTDKHPHTNMAKAALNMMTLTSAPDYARDNIYMNAVDTGWVTDEDPAQHAERKVQELDFQPPLDIVDGAARVVDPIIASENSGEYVWGNFFKDYRHTAW
>NZ_CP017172.1|WP_140796359.1|1395856_1396282_-|hypothetical-protein
MTSMKGISTEMHPYLRMTAPPGVTGLEDVPFEPGQPLFRSKLLLGGVLPVGWSDLTLRELEPGRRFVEESPMSAMRQWRHERRIVETHAGVDIIDQLDFEPRFGGRLAEAFIRRLFEHRHSVLRRALTPSIGGRASQEKPA
>NZ_CP017172.1|WP_140788104.1|1395523_1395850_-|TerB-family-tellurite-resistance-protein
MSPEEQFHVEVLKLLLQVATVDGRVAHSEIGHILDTARGMSVPLPELAALTRCLRNNEPLPPPNMGILRTNPSAVIREAKALIASDGSVHAAEIEMLRQIRELLGVIN
>NZ_CP017172.1|WP_090484863.1|1394164_1395508_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MSSARILVVDDDPQARDLLQRLLGPLGAVTQAPDPRRATERIAEGAFDLVLTDMAMPEPGDGLKVLHEVKAQLPDTPVVVVTAFGNIEGALDSIQQGAFDYLAKPFDVDAILRVARRALEQKRLVEENRSLRQQVERGSLMLVGRSPALLEVYKHVARAAASNVPVLITGETGTGKEMVARALHKRSPRMNGPFIPVDCGAITESLMESELFGHAKGSFTGASGARRGVFEEASGGTLFLDEIGDVGMKVQSQLLRVLQEGEIRRVGESVPVKVDVRVVAATNKDLKARVAEGLFREDLLYRLDVVHLHLPPLRERSEDIPALVEHFAGRHARGGVRPVVTPEANARLAAYDWPGNVRQLENVVARALALNVTGVLGPQDFPEPIGDASTPKMAGLAGDMPSLAELSRRYAAQVLQHVGGNKSEAARLLDVDRKTLYKLLEAPEAES
>NZ_CP017172.1|WP_140788102.1|1392737_1394168_+|MCP-four-helix-bundle-domain-containing-protein
MASSRIPIRGYRAGFFFVVVLLSAVTAFTLWTEVRTGSQVDGLVQEALERAGSIGRIRVDALSLEAAIEAHVRATGDAERRAADAVMEQILADIRASSEAYTRNLPQGEKALWYRFNAACQGLADQVRAAAIFSQRREAERARRHLAERIRPLAAELDALGGALEEENAAEARRLVNRLEDLRVRNTALGAGATLLAILLSSLVGWRVTSLLKRQEAIIQGQLEELGRHNQELDAFTRRVAHDLISPLAPLKGYLTLIRRTGAVNDAGALEMLAQCESSAVRMGELIEALLRFCRAGTRGESTVGELDTAVTTVLLEVAQTAAAQGVALERELEPGVAVDCPGQLLQVSARNLLTNAVKYSEGRPDPRVKVRVATEDGMAVLEVVDNGIGMAPGTLASLFQPFFRAPEVRGLPGHGLGLVTTKRVVEAHGGTLVVRSEEGKGTHVVVRFPRVVRPAAATSGSQATTASAGMRKVGT
>NZ_CP017172.1|WP_140788100.1|1392224_1392692_+|hypothetical-protein
MRFLCFATALAVLGTGCATGIPLERLEAQVLESDRWRREYEAERERAEAFALRMAQLESALERVRLERAEAEQGRAALLEELVRTEADRHALEEHNTQLLALEREVNELKELKEMHEELSDVWYESALERARRRLNNPPQPAALPAAGNVAPTVP
>NZ_CP017172.1|WP_140788098.1|1391692_1391926_-|hypothetical-protein
MKTVFAAALLAAATAFANTPAPAAEAKPAAVEAAPEAAEAPQAEEAKAEAAPEAKPAKKAKKPAKKAAKSTTATEAN
>NZ_CP017172.1|WP_140788096.1|1390815_1391406_-|GAF-domain-containing-protein
MIEAFSKVSEASKLLLEKGLGPSTGMEALSMVGHALGVDRAYILENRVQGTYGRFITDMRYAWAEPPTPSPLANPVMRAFSFREFAPGWVDMLEAGMVVACPTRDAPPMMKDLLERQGTQSILLCPINPSRQQWWGMVAFEDCRRPRAWKPEEVTLLKSLGRAVAASVRHGQMRSSLDQVRNSLRQAVSRTPVSGL
>NZ_CP017172.1|WP_140788094.1|1388846_1390700_-|protein-kinase
MSSIDPTAISRPRSPDIISGYHLDKLVGSGGMGEVHKATQLSLGRTVAVKLLNPELAKDPSFIARFQKEAAALAALSHPHIVSIVDKGKTDTTYYLVMEFVDGPSLRELIREPHLDVVGALRRMLQICRAIEYAHGRGVIHRDLKPENILLDQQAGGIAKVSDFGLASFLDDASPSSRYALTSTHVSMGTLSYMAPEQRVDAKSADARADIFSLGVILYEWLTGEVPLGTFDPPSRRKPGLDSRLDAIVTRCLKPDPEDRYPSVTSLIADLELLVPGSLPSLAPVKLTHLQRVRQGVRKVVRMALQAAAVLLVMAALAVLGREWLRSGEKPVPPQPGAALNADLGPPSPRSMPGRLETGSEKRTVSVGDGPDAPSLLVAGRPVEAEEKAIIFPPVEERSQSRVGRARVDVVGLDGDIAVLSARVRADAPPDTWKRRGYVMLYGPSLQAPSAALLLQGSTGRYVALIHDGAGAPLRLEWALGERRGTMLGLASPEGEAALELRVDADGVMQGYVGKGKDQRAIGEPLNLGPGWMEHFGDAPVPAFGCIEGTCRAEGFLYTVRRAPPPGTTAPVPDVPVTKAVVAAVPAKAVPAKRPPPPPPPKKQPAKAPAKSPPKRR
>NZ_CP017172.1|WP_140873474.1|1384981_1388761_-|tetratricopeptide-repeat-protein
MRTIRLGFAALALVTALTGCHRSTSTATPRVLESAAEQAQKGTQQARTLAFAGFHALLVAGDATLAQQRFDDAIARDAGDVYALAGQSLMARRAGRPDRALSASLEMVARAPTHPLAAVAARHVLDSVGTSRSLDDDILRGVERALAAGATGEAAYLMRGARMSVAVVRGDAEARDAAMRQLGGVSEVSLVGPFSPFHVLAWDESTSVSQSGSLAGPFTGAFGPLPVRTVRAPDGRMDLTGEPGQGDLYVQAFDADVTEPGLYVARTVSGTSHQVLMDGAPLMERRAWERATSTVTARAVQLPAGKHRFVVRQLKGGTSGLLTFALLRVDGRPSGVRFSTATGAAPQAWGSKAEFSDETPGVFPTTEGLKTALHEEAGELLAVMLAVRDGLQRDADGARRLMASVDANTPALLWLRAEVASADRTVPSKVARGRATRDLESVLAKDPGNVAALLLRAELFLDEGQPTSAMDMLKTASEVAQPAGHPVFMLRARAALALEVEALAEESLAAALEAQPGLCEALTLQYSLARRRDAAERSDTLAASLNGCPGTVVRQAEHARTRGDMETATKLYSELQARDPSSISLANTLANLYVSKRRFDDATAVLQKLATVWPRNAELVKRMADVREYAGQPAEALKLREKALAMAGDDLTLRRTEERARTGRELLQAYAVDGREAIRAYEAEPVSGGSAAAFVLDAAAVRVYPDGSIVNRIHTVQKALEQSGVQEIAEVNVPRGAQVLALRTLKADGRVLEPENIEGKDTVSLPGVAVGDYVEVEYLLAEPPRGPAQPGFTASAFYFQIANQPNAWVTYTVVAPKGVGMKVDAHGMKVPEPKVDGDLEVFHFETRRVPPFIPEPDAPPSANEYLPFVIVGAGDTGNESLVKLYGDAFLERWLRTAEVDAFARKAAEGKSGLDAVKALHAAVMQRFSGRDASLSQTAASTVAQDRGSRLTVMKAGLDALGIPSRVVAVRTFNTDPSAYTFPQDALLPYAALRVEVPGTEPVWVDTSVRYGPFGELPELAMGEREAWLLPEPGRPLQKVQTPPLKETPGKEVKLALKLAEDGTLSGQGEETYSGFEAAQIAEAFNQLSAESRNQALQGAVARYFGGASLSSVKLENQEQVGAPFVLRYEFTVPRFGRMEGGQRMALGPLTFPAQLGRRFVQLSTRRTPLYIDTTEASRTQVTLSMPKGWKLADPQASLEANNAFGRFTRSEKQDGSTLSVTESLRVPRNRVMPGQYELFSGFTGDVDLIQTRELVLVKP
>NZ_CP017172.1|WP_174259409.1|1398687_1400295_+|L,D-transpeptidase-family-protein
MFAAWQRTAADAGTDGGVDGSAEAALSPPRRTPDDGATVARDEVPALTIDPALDDLAQSEEEEDTPGEEEVPPPEQLTVIPDELHPGEELVLGPDGEPLEDTGLVLEDVDPGLEPVSGAEDGGTYAVPFAPDAGSLRVRRSIVVRQEPRQDAPALGTVAQDMRVRWQGETAVRGPDCEAWIQIEPRGWVCERYLEPNFREPRVRELPKLREGELTPGIYARVVGKRVRAYPSLALARARRKGVLLKGSVSVQLRGQVRIRRRTYWRTTDGQYLEARVLREYRPSSFEGVNAEAIADLPPTFAWAQSRTRPTAAVEVRTAPDAKATRETVLPPRTMVAVKELSEDGHWVSIAEDQWVARDDLHVAWFSHAPPQVEPGSRWLDVDLDAQVLVAYEGERPVYATLISSGKQGTDTPEGLFRIWIKFAEADMTGSGTAGNDTYRVATVPWTMFFQDDYALHTAYWHDRFGQPMSHGCVNLSPKDARALYSWAAPQVPVGWSMVHATEDAPGSWIRIRGQARPTGKPRKVAVAATQVGAP
>NZ_CP017172.1|WP_011551294.1|1400298_1400712_-|YjbQ-family-protein
MFHAKELTVSSRGRGFTDITADVQRAVAESGARQGLCTVFLHHTSASLLLCENADPDVRRDLESFFSRLVKDGDPLFVHDAEGPDDMPAHVRTVLTQNALNIPVKDGRADLGTWQGVYVWEHRTSPHRRRVTVSVVS
>NZ_CP017172.1|WP_140788108.1|1400715_1401450_-|dienelactone-hydrolase-family-protein
MERALRHVATRLGELDCHVIDALPEGATPELVVVLSHGLGAPATDLVPLGPELMAFQPALADRVRFVFPGGPMAWAHGGRAWFPLPDAVMRGEQRDWEQFARDVPPGMPAARRALMSTVDALCAAMKLPYGRIVLGGFSQGGMVSTDVALRLDEPPAGLCILSGTLTSEPEWRTRAQGRTGLPVFQAHGRYDPLLPLGNAERLRDMFVASGLTVDFHAYDMPHAIVTEELEALAAFLAARLGGR
>NZ_CP017172.1|WP_140873476.1|1401452_1402199_-|peptidylprolyl-isomerase
MRTQFLTTVLLCLTLTACKDSDKKESTGGGTPPSATTPAKPSAPSAAEVPAAAPPAEAASGEWTKKVQAGQDVYATLETNQGAIVVRLFSKDAPKTVANFVGLATGEKAWTDPKTGQRVEGKPLYDGVIFHRVIPGFMIQGGDPTGTGRGDPGYRFEDEFQSGRTFNKKGLLAMANAGPGTNGSQFFITTSTPDYLNNRHTIFGEVVSGYDVVEKIANVQRDPRDKPLEPVVIQKIAMSDQAPAGSGN
>NZ_CP017172.1|WP_140873478.1|1402388_1403354_+|hypothetical-protein
MAPPIRRNEPRPVPTPPVTARPTPPPPPPPPARAEARPAQADRFEDAHNRVTQAATGLRSVSDAAVATQVRDAFGPRRFGPVNLPGGNGPVVEGANTRLARGAGAVSLAANVAQLPTGAVETFRDVRDALRNPTEANVREAVGTASGTLSTGLMAARDGLNLAGNVSNYRAATDAARTAFTAAAPEASRAAANRVATTAANTALEGASRQVVRRAAAEVAERGLEGAARTAGTAARAAVQGGGTAVARAAGRFTPGLNVAIAAADTVAAVNTITDPNASAGKKITAGVTALGSIAAATNIPVVSQVGAAVSTVSGFIGSFF
>NZ_CP017172.1|WP_140853205.1|1403307_1404540_+|peptidylprolyl-isomerase
MRPSPPCPASSAPSSRKRRVVNLNAPGGFGPAGALCYPRGTERETMTTHDDSQGGRKNARSLAELHALGIMKKMPAALQLDSTEPVELPTVEAPSLEGVSVAQVAPAPLTEQELVDRFDALRRQHADVRERQPGEDVALEDDVLVDVLGFANNRLMPFSVRENWWVRVAADPGLPGFFESLAGAKVGQSVGIELTLPDTYPVEALRGQPARFLVSVKAARELKLLDDDSPELLSRLGMGSITDVMRKLGDDLAQARLADVDRLTQERVMDVLVDRTPVEVSAALVDEEIRRRWAEAERPILQRKDFQPDELQEALEGWLQDPLTRMDAAYRITLALVLRAIAERDGIQPDRAATDAMLEDLANFTGVNRQELGVAVKEDEALARRLYEMALRFSTIDHVMKKVTLTPAAA
>NZ_CP017172.1|WP_140873479.1|1404543_1405755_-|lipase
MSASKSAASAAASLRLPGTQPLASTSHSCPVVSFEILPSPDVLSRALPRVRPQVTPWRARRYVGARLGLPGTLPLEMTPSQPEAPHAPSTHAAAPSAITRLARTLRGLPPAERWWGPGCAGMAGWLKRAAQSLPPEDLTPRFHALLARVRQGLPVLPQEARRHQYVLVRGMLGDELPGYLLDNVQRLERRGLSVREAAVDTEGLLADNVAVLREVLRDAEYFGRSVVMVGHSKGGVECTATLALYPELRHVVRAVVTLQAPYGGSSIAHDLATTPRLRRLIDFAFPLLFHGVSRSVEELSYPQRQAFIQQHPYPADIPTVSLATSRLSRTSTLYPLQRYLHERYGYQADGMVTAVDAEVPGARVVRLHDMDHAEAALRGLPGMVRYHPGDLTEVMVALALETR
>NZ_CP017172.1|WP_140796361.1|1405657_1406008_+|adenosylmethionine-decarboxylase
MTTGQEWLVDASGCVPGSLKDAAALAALFEALIVVLDLKVVGQPQWHVFPEPGGITGLTLLAESHLGIHTFPEHGFAALNVYCCRERQRPDFEALLARHLGATACVVRELKRGVTA
>NZ_CP017172.1|WP_140788118.1|1406004_1407900_+|DUF4178-domain-containing-protein
MTQGKCPSCGAMVEFTAGSAQVVVCGYCQTVVARKGLDFESHGKIGSIVPTDSPLQLRAEGRYRKAAYTIVGHLQKDHGAGPWDEWYVEFADGRTGWLSESEGAFHLMFDMGPEEGVALEDLHPGERLHLRDRAWVIEERGHGRVVAAAGQLPSDVDPTQDAWYVDATGPKGAFLTLDFGTRGHSPEAFVGEALKLEQLGIPAGQLRPRVRKVELQQARCTQCNGNLELRAPDKTLRVACPYCGALLDARQGKLSFLRMLQKPSRPLIIPLGTKGKLDGAEWICIGYLERSCTVEGVRYPWEEFLLYNASRGFVWLMNSNGHWVFLKPLPAGDVSLSPDVAAFYEHRRYKCFQHVTAVTDKVLGEFYWTVRVGERAEASEYVAAPYSVNVDATDDEVSYTHGEYLEPEVVKEAFGLQEPMPQREGIAPSQPNPHQSGLRSVFVWTGLWILALFVLAAVLSLTAAKTVVLEEAVVIPPDATPGTPGAMHFSEPFELPKRGNMRVEISGTPFNEWLGIQGDLVNQDTNDVVLFYEELSYYRGNDGDGEWTESNMSASTYLSPVPAGKYALRTTASFAANPVRPRPMTYRVKLIHDTPNSSWFCFALGLMVVGPVVALYRSHSFETRRWAESNV
>NZ_CP017172.1|WP_020478251.1|1407932_1408094_+|hypothetical-protein
MKWFGGLVLLGYAALTISGWSPFTKEERDKVPGNVRRGPGGVLLWTGGYMGGK

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_6

2223590-2223687

Orphan

Consensus_repeat	Method
CTCGGCCGGCCCCGAGACGGCGGGCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_6

>merge|NZ_CP017172|6|2223590-2223687|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGGATTCTTGTAGGGCGCTCCATAGGGGAGCTCCCGACGCCCACCGCCTCGGCCGGCCCCGAGACGGTGGGCGG

>NZ_CP017172|6|6|2223590-2223687|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGG	ATTCTTGTAGGGCGCTCCATAGGGGAGCTCCCGACGCCCACCGC
CTCGGCCGGCCCCGAGACGGTGGGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140789070.1\|2213231_2218079_-\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP017172.1\|WP_140789093.1\|2233251_2234436_+\|PLP-dependent-transferase	unknown	unknown	gnl\|CDD\|99738
NZ_CP017172.1\|WP_011552040.1\|2222370_2223294_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187551
NZ_CP017172.1\|WP_140789066.1\|2208942_2210520_+\|glycosyltransferase-family-39-protein	unknown	unknown	gnl\|CDD\|281842
NZ_CP017172.1\|WP_140789095.1\|2234432_2234927_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	unknown	unknown	gnl\|CDD\|236483
NZ_CP017172.1\|WP_140796396.1\|2211804_2213085_-\|serine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235461
NZ_CP017172.1\|WP_140873927.1\|2235408_2235963_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239516
NZ_CP017172.1\|WP_140789064.1\|2207696_2208905_-\|DNA-polymerase-III-subunit-gamma/tau	unknown	unknown	gnl\|CDD\|237871
NZ_CP017172.1\|WP_140789083.1\|2227955_2228339_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140789068.1\|2210899_2211364_-\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663
NZ_CP017172.1\|WP_140873923.1\|2230737_2231508_-\|DNA-repair-protein-RadC	unknown	unknown	gnl\|CDD\|178801
NZ_CP017172.1\|WP_140853546.1\|2220400_2221339_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|200565
NZ_CP017172.1\|WP_140873918.1\|2218285_2219599_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224153
NZ_CP017172.1\|WP_140800643.1\|2230486_2230738_-\|DUF3006-family-protein	unknown	unknown	gnl\|CDD\|378598
NZ_CP017172.1\|WP_140789085.1\|2228352_2230440_-\|RecQ-family-ATP-dependent-DNA-helicase	unknown	unknown	gnl\|CDD\|223588
NZ_CP017172.1\|WP_140789079.1\|2221480_2222335_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153249
NZ_CP017172.1\|WP_140789089.1\|2231665_2232124_-\|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|237999
NZ_CP017172.1\|WP_140797724.1\|2219672_2220383_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133022
NZ_CP017172.1\|WP_140797729.1\|2232196_2233159_+\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP017172.1\|WP_140873925.1\|2235147_2235399_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140789070.1\|2213231_2218079_-\|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.	2.34096e-40
NZ_CP017172.1\|WP_140789093.1\|2233251_2234436_+\|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.	1.54203e-134
NZ_CP017172.1\|WP_011552040.1\|2222370_2223294_+\|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_CP017172.1\|WP_140789066.1\|2208942_2210520_+\|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.	1.32281e-19
NZ_CP017172.1\|WP_140789095.1\|2234432_2234927_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	gnl\|CDD\|236483	PRK09364, moaC, cyclic pyranopterin monophosphate synthase MoaC.	4.41573e-75
NZ_CP017172.1\|WP_140796396.1\|2211804_2213085_-\|serine--tRNA-ligase	gnl\|CDD\|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP017172.1\|WP_140873927.1\|2235408_2235963_-\|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.	6.16398e-42
NZ_CP017172.1\|WP_140789064.1\|2207696_2208905_-\|DNA-polymerase-III-subunit-gamma/tau	gnl\|CDD\|237871	PRK14965, PRK14965, DNA polymerase III subunits gamma and tau; Provisional.	0
NZ_CP017172.1\|WP_140789068.1\|2210899_2211364_-\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	9.21008e-66
NZ_CP017172.1\|WP_140873923.1\|2230737_2231508_-\|DNA-repair-protein-RadC	gnl\|CDD\|178801	PRK00024, PRK00024, DNA repair protein RadC.	1.10803e-73
NZ_CP017172.1\|WP_140853546.1\|2220400_2221339_+\|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_CP017172.1\|WP_140873918.1\|2218285_2219599_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|224153	COG1232, HemY, Protoporphyrinogen oxidase [Coenzyme metabolism].	1.59499e-43
NZ_CP017172.1\|WP_140800643.1\|2230486_2230738_-\|DUF3006-family-protein	gnl\|CDD\|378598	pfam11213, DUF3006, Protein of unknown function (DUF3006). This family of proteins has no known function.	0.000422016
NZ_CP017172.1\|WP_140789085.1\|2228352_2230440_-\|RecQ-family-ATP-dependent-DNA-helicase	gnl\|CDD\|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	9.44418e-156
NZ_CP017172.1\|WP_140789079.1\|2221480_2222335_+\|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_CP017172.1\|WP_140789089.1\|2231665_2232124_-\|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_CP017172.1\|WP_140797724.1\|2219672_2220383_+\|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_CP017172.1\|WP_140797729.1\|2232196_2233159_+\|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_CP017172.1|WP_011552040.1|2222370_2223294_+|SDR-family-oxidoreductase
MKPAVVVTGISGNLGRTLAKLLHKHERIIGIDRRPFAGRPKDVEMYELDLRKKKAEDVFRKNEIRAVIHMGIMHDPRMSEEEHHSFNVVGTTRLLEYCAKYGVKKVVVLSSANVYGPSPDNSNFLTEDAPLMAASRFSGVRDLIEVDMLAHSFFWKHPHIETVILRPVHIVGPTIKNAPSNYLRMRRPWMMAGFDPMVQLIHVEDVARAMVEALRPEPKGVYNVVGPGEVPLSAVMRELGNTPIPVPHPVARPLLGMLFKYRLANFPPPELDHIQFLCAVDGSRWVKDVAWKPRHSMRDTIRSVQGD
>NZ_CP017172.1|WP_140789079.1|2221480_2222335_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MLENVTDRVKKGLREWTDRLANNEQKQRLDGLARPGNEYGVDPFGFDLDYSLSAVAPLLWLYRNYFRVETFGIEHVPAGRVLLVSNHSGQLPMDGAMIGVAMMLDASPPRVIRSMVEKWVSSLPYVSTFMARVGQIVGTPENCRRLLESEEAILVFPEGTRGINKLWPQRYQLQEFGLGFMRLALETNTPIVPVAVIGAEEQAPALMDLKPVAKLLGFPSFPITPTGLPIPLPTKYRIYFGEPLHFSGRPDDEDSELDKKVRTVKASIQSMLHQGLKERQGVFW
>NZ_CP017172.1|WP_140853546.1|2220400_2221339_+|polysaccharide-deacetylase-family-protein
MRLASISVDLDSLPHYCRIHGLPESLLGARARSLVHAVAVPRFRELLDGLGIPGTFFVIGEDLESDPVAVAGMRASHEAGIEVASHSHAHDYALTRRGPEAIHADLARADAAILAATGARPEGFRAPGYTLNADLYAATAALGYRYGSSAFPAVPYYLAKAAVMGALSVLGRPSRSVLDTPRVLLAPRVPYRPDPAQPYRRGSGTVLELPMTVTPALRFPLIGTFATTLPRASLHALWRTCRRDTFFNFELHGVDVLDASDGIPPELVRQQRDLRVSATQKMARLREVFGWLKSEREVLTLRDVAGRLSASV
>NZ_CP017172.1|WP_140797724.1|2219672_2220383_+|glycosyltransferase
MAPHLTVVIPVYNEESIIASAAEELRQGLDARGLDYEIIFAENGSRDATPAILEELCANNSRLRWFHSETPNYGVALKAGILKARGTYVICDEIDLCDLTFYDAALPRLERGEADMVVGSKAAKGASDQRPLIRRAATRVHNKLLKVALGFQGTDTHGLKAFRREALLPVIQKCVVDMDVFASEFVIRAWREGLRVMEIPIQLHEKRQPSIHLFKRVPNVLKNVGKLFYVIRVRGT
>NZ_CP017172.1|WP_140873918.1|2218285_2219599_+|FAD-dependent-oxidoreductase
MEPIVILGAGLAGLSTAHFLNKPWRLIEKSDRVGGLIKTEVIQGCYFDPTGHWLHLRDPEIQALVNTLWLPEQMVRIQRKAGIFTRGVFTRFPYQVNTHGLPPEVVAENLTGYVEAVYGEKGHELREREPRNFEEFILRYMGEGFAKNFMVPYNQKLWTVHPREMSAAWVGRFVPRPNLKEVVDGALGAGSDAVGYNASFLYPREGGIESLARAMLSHLKGGQLSIHTEPTAIDWKARKVTLSDGSVQSYAGLVSSISLPGLVKLLAKGEAGVPDTVQDAAKQLRATTVTYVAVGAKGANRQPWHWIYLPEPEFHTYRIGSPSAVYAPLAPPDTSTFYVEYSHHGELSPAAAEKYAVEDLVRSQMIHAADDVLFAQAREIPHAYVLYDEAYGPAKSEILRFLEHAGIQIAGRYGQWEYSSMEDAILAGRACARTLNG
>NZ_CP017172.1|WP_140789070.1|2213231_2218079_-|zinc-ribbon-domain-containing-protein
MKVSCPSCQTNYNIDDKRIPPGGAKLKCARCQTTFPIKLEAVSAPSAPAPAEPAQATAIPLPGATSAAPLTAAIPLPGATSAQAAAIPLPGAASAQAAAIPLPGAASAQSAAIPLPGAPASAQSAAIPLPGAPASPGAIPLPGAAPTHSAAIPLPGAPASTGAIPLPGAASAQAAAIPLPGAASAPSAAIPLPGAPEAFGAAPHAAAIPLPGAGAPQPTAIPLPGGAPEADPFAFDMGEPEQAAAIPLPGGAPEADPFAFDMSEPEQAASVPLPGSAPEADPFGFDMSEPEQAAMPLPGAAPEEDAFAFDMSSPAEAAAAMPQAGGPSDMDAFGDDFGEPVRDTREVTRVVSIPLPSDAYREPPAAPASGYGVNEPAGTARDFDFETVEAPVEDAAQGYGVNAPASTARDFDFADDALPVPVEAPPAEDAFAFDIESSSGAAQAQPPQEDPFALPPPAAYAQPAAPVDDPFALPPPDMAPQTDAFAPDAYAMPSAPEASPYAMPPPAAGAPSFDFGELPVPANADPFALPPPGADFSDLPAPAAPQALEFADLPAPAAPDLSFDFNEPPAPGADPFAVDFSAPPAPAADPFAADFGSAPAPGADPFAIDFSEPPAPAPAVAVNPAVDFGDVDFGAPSSPGIPDSLEFDPTARPDDDLEADLSDPLPPPPNAGPADGLEMLSFIDDAAGKDGGAQAGTKVRRFHVRRRSGKVFGPFDEGVIVKMLEDGQLLGNEDVSLDSETWSAIGTVPTFAAAIQRLMEGPAKLVTPTAAPAAAVIDAPRVDGASPQANMKRLEQLYEGRMAAVSVVDRSGNTEKWKKRVPLMIAAGVAVVVAGIGAGTEFGTRYGAFGRRALFPTRLSDGSAEAKQVADAKQALLTDTFASYKQARELSAKVLAQKEYPEVRSLWCQSVYYLQRRYAAGNPNEMSRCRQDMADIEFLGEKDVDVIKASAAIALTSRQADSVIPTLSGAYGREDTQGDLELAFLLAEAYSQKRDEKRALDTLNKVLAKNPKSAKAHHAVGNLHQAADRADEAAAAYAAALEADPKHVASAVELAAVELLVRKDVAKGTEAVERALAEDVQSALGPAELARARGLKGVAMFQKHQPKEAEAELKAALEMDAKSTFLRGQLARVLRAQRNFEGALPIYKALATEEPNNLEFADGHITALVMTGKMQDALEAVKKANGVFPNEARIAYLYGRIEDALDNLSDAEGHYKRAIAADDNLVEARLYLGRFYLAQRRNAEARPQLEEAAKKAPENAGVRAGLGELALAENNTLLAQQEFERSVKLDPILADAHLGLSRVALLTDDLETAKAEANRALELDPHLLKDGRLQRGLVLWRLGQLEEAVAELEKAKTEDPRSTTIPITLGAVLLERGDLPGAESNLGLALSNEPSNHEALYYLALVKAKRLEFTQALDNMRKAVERAPNRPDYHYAYGVILRDAKNLPDAMSAWRKTVELDGTHADAHEALGHALLEGSQFDEAITSFEASLKADPRRTRVLGSIGDAYFAAARWNDAIKRYQSALKADPKLTYVYYKVARAFTEQAQHAKAIDWYRKATSLDSENPMAYYYLGFAYKERNKRREAVQAFKDYLSRKPDATDKKDIEDEIYDLQN
>NZ_CP017172.1|WP_140796396.1|2211804_2213085_-|serine--tRNA-ligase
MLDLRNVAQNFDAVVARLKTRGGNLDLGPFQRLFAERRELYVSVESLAARRNAANEEMKRKAKEDPKALDALRGDLRAVSQEIKEKEARLKDVEEELNRILLLIPNVPHESVPEGGGAEDNVQVSIWGQKPDLLFAPKQHFELGEKLGMLDFERAAKVSGSRFTFYKGALARLERALVTFMIDVHTSKGYTELLPPYLVLRETMMGTGQLPKFEDDAFKTLGEPERFLIPTAEVPVTNYHADEILEGESLPIRYCAFSPSFRAEAGAAGKDTRGLIRQHQFHKVELVKFAHQEKSLDELEAMTDDACDILRRLGLHHRVMLLCTGDMGFSARKTYDIEVWLPGQNSYREISSCSDCGDFQARRAKIRYRAQRGDKPQLAHTLNGSGLAVGRTTIAILENYQREDGSVAIPEALVPYMGGLKELKPI
>NZ_CP017172.1|WP_140789068.1|2210899_2211364_-|nucleoside-deaminase
MSDEAFMQQALSLAREAAELGEVPVGAVAVFNGEVVGAGFNRREVDRNPLAHAEMLAMDAAARKIGAWRLSGVTLYVTLEPCAMCAGGLVQSRVTRLVFGAFDPKAGAVGSLYNLVEEPRHNHRLQVTSGILADESRLLLKTFFGRLRAKKRDN
>NZ_CP017172.1|WP_140789066.1|2208942_2210520_+|glycosyltransferase-family-39-protein
MSLPSHEVGFHSPSGSAPGRADERFTPCVRERGREESAAPVSAPLLAAPTDSIPTPEPTSLAPGGTPQVAPVRNWMRWVLGAVALLPGLIAVVQLGRIHPDEVYQSLEPAWWRVHGYGVLAWEWRDGLRNWAVPGVLAGFLKLADLLGITHPRAYRVVVAIPQVALHAWSLWAAYRFAQRRAGTAGGLLSTLLVGLYGPLLVFAGRTMAESISASLLVVAVEALDRRERLARAGLVGGMALGLAVVARYPSAIFVLAALVWLAAARRWRLLAFTCAGGLGVAVALGALDWATWGSPFHSFFAYARFNVFSGKAAAQFGADAPSFYVKPLLTAVPLWAWAAVPVGIAALRQHRALSLPLWCAAVYTGVLLATAHKEERFLYPGLVLGVLAAAPPVAAGLVQLARPTGRWGLAGLALVASMTAAAFFPSGDLRADQFRAIVAATRGNARGLLIVNEGLWGSGGFFYLGKQIPWLTCDWPHDGAFQRALRDRTFNRAVTFEDRALAELQAGGFQIVRKVGRETILSRE
>NZ_CP017172.1|WP_140789064.1|2207696_2208905_-|DNA-polymerase-III-subunit-gamma/tau
MSYLVLARKWRPQKFDDMTGQEHVVRTVANAIKMDRVAHAYLFCGPRGVGKTTAARLLAKALNCEKGPTAQPCGECRACTEIAAGTSVDVAEIDGASNNGVENVREIRENAKYLPQRDRHKIYIIDEVHMLSGAAFNALLKTLEEPPGHVKFIFATTEAHKLPDTILSRCQRHNFRRIPAARMLQRLQEICKAEGAGISDRSLSLVVRQSEGGMRDALSLLDQVLASCGANPSDEEVADALGAIDRTLVQDFADALVHKDAKRVLERVEEVFNRGLDLKRLAEELAFQLRHLFVTKTLGKAPDELAESEQKALMALAQDAEAAQLTRLFDVVHGCIWDVSRAAQPRLALEMALLKAIQLSPGGSIPELLARVDKLAAGMGEGSAKSNAGAPGGRSSPANFRA
>NZ_CP017172.1|WP_140789083.1|2227955_2228339_+|hypothetical-protein
MRYFSSRTDSPLLHIMWGNAFLLSLIYLLLGLGVEIALRYFPSRFLQRLSLSLDSLPARALELTGAMEPLRAAYFSGRISEVGVRVVFGITTMVVIFLLAMVVGTVMGGVRTLLARRALREGGRRHP
>NZ_CP017172.1|WP_140789085.1|2228352_2230440_-|RecQ-family-ATP-dependent-DNA-helicase
MMNMRAMPVDLPYLEEAQQGLVRHFGLSQFRPGQDQVISSVLSGRNTVVVMPTGAGKSLCYQLPATLLPGLTLVVSPLIALMKDQVEQLTARGIPATFINSSLSDLERAERMRKLRAREYKLLYVAPERFRSQSFLETVSALGVDLLAVDEAHCISQWGHDFRPDYALLGQVRKRLRPPRTVALTATATPEVRADIVRVLLMKDPQEFAMGFDRPNLFLGKQEVGGDADRHEACARLASTGGSGIVYCSTRRAAEDIFSELHGRGVKAVLYHAGMDDDARRRAQDTFMSAKEAVAVATNAFGMGIDKPDIRFVGHANIPRAVEAYYQEIGRAGRDGQAARAVLLFNHSDVFTQERLIQSSHPAEAIFGDVWNVLQSVEEFERGVHALAGTVNASEFEVSAALRILEREGKVERGGRGEGEHGITLLEKATSAQPHSPDAQRLLKSLLETFPVGRQVTTELPILARRIGLSVDEVRHALGLLEKAHVVKVRRPFAGRSIRALERVPFRELGLDLSRVREQERQNLSLLRRMTEYAYTDRDKKCRRSAILRYFGQRDTNTSCGNCDVCTPEKMPTLLAHGPAASRSRGTGSAAAPVVTNYSELASTELRRWRKELSKDLGVAPFIIFNDATLLGLSAALPVDREGFLAVKGTGESRWERFGPKVVEICLMARAAGHEPQAVPDAAVRARKPTIRRRS
>NZ_CP017172.1|WP_140800643.1|2230486_2230738_-|DUF3006-family-protein
MVSMVGLWGAVQVELLEDVRAQVVRLDTGQACTVERASLPTGVREGDVVVDGRLEPGQTEARRQDVARIRARLAVPVPPGFDL
>NZ_CP017172.1|WP_140873923.1|2230737_2231508_-|DNA-repair-protein-RadC
MEQAAAGAAWAGEGSVRARGVGGAEESRERLFRLGAAALTDPELLCLVWSSGPRAPGAWAVAGALLSEGGGLKGLVQQEPLALSLRPGVGPVRAAQALAALELGRRSQRAGERRPRLRTPKEIATYLAPVLGALRREVFHVLCFNARNVLVHDARVAEGTMNTCPVDPREVFAAALTSRATSIVLAHNHPSGDPEPSVQDLGLTRHLVAGAQLLNIKVLDHVVMGDGGYVSMLERGLMPDEAQEKRRAWSANGGGG
>NZ_CP017172.1|WP_140789089.1|2231665_2232124_-|cyclic-nucleotide-binding-domain-containing-protein
MDAAVLKKVALFEGLTQGQLAKVAQIGHSRTYPAGAFLFREGETGQEMFVIAEGKVRISKSVPGIGEEALAILEPGQYFGEMAVIEDSPRSADAIAHVSCAVWVIERSRLDQLMFTDKDLAYVLLWTFVRTLSERLRETNEKIKGFFALSRF
>NZ_CP017172.1|WP_140797729.1|2232196_2233159_+|thioredoxin-disulfide-reductase
MVEEKINKVTIIGSGPAGYTAAIYAARANLQPVVFAGGPTLEHPQRVPGGQLMVTTDVENYPGFPEAITGPELMERFQKQAERFGTTIHMENVVKVDFSQRPFLIQGESVSCRSETVIISTGATAKWLGVKGEDTYKNRGVSACATCDGAFFKKQDVLVVGGGDTAMEEATYLAKIVNHVTLIHRRDTLRASKVMQERARQNPKISFMWDSAVEEVLGDAKGMNGAVVRNLKTGDSHQVKATGLFVAIGHTPNTELFQGVLETHQGGYLKTVPGSTRTNIEGVFACGDVQDHYYRQAITAAGTGCMAAIDAERWLIEHGE
>NZ_CP017172.1|WP_140789093.1|2233251_2234436_+|PLP-dependent-transferase
MSSKQKTVAVHAGTRLAGSKAVPVSPPIYPAAVNWFDSSDDLDSALDGKDYAYARISAPNTTLLEEAVAALEGAEACVAYASGMAALRSVFEAQGFRAGDTLVMPADGYGVTRALYKSLCATLGVELHAFLMTDPEVPGRIRELKPRMVLAESISNPLLRVPDLRVLARACQDVGATFVVDGTFPSPVGQRALALGADYAVQSTSKWLNGHSDALGGTVSASRERMAPLRAARVLAGDVLGPFEAWLTLRGLRTLPVRMKAHVEHAAHVARRLAESPLLERVIYPGLASHPDHATAQELLLGGGPMVAFEIKGAGRPECMRFLEALKVGRPGPSLGDVCTLVMHAASASARRFTPEEREAAGIRENLIRVSVGLEDPDDIVDDLLAAVAQGVRR
>NZ_CP017172.1|WP_140789095.1|2234432_2234927_+|cyclic-pyranopterin-monophosphate-synthase-MoaC
MKMVDVGGKPKTGRVAVATALLRMLPDTRERILAGKVEKGDVLAAARLAGIMAAKRTPDFVPLCHPIALSGVEVTLAPEDAGLRVRVQVKTVDRTGVEMEALTAACAAALTVYDMCKSVDRGMVLDAVQLEHKSGGRSGTWRREEATPAEAAAPRRRTRAKKAR
>NZ_CP017172.1|WP_140873925.1|2235147_2235399_+|hypothetical-protein
MSDLRGVLTLLTALGAAGCGALTEEGAAADVSQPVADRAACDAQAAQRRYVSEDRKECQVVFFVCARGESPFFDACGCGCSRP
>NZ_CP017172.1|WP_140873927.1|2235408_2235963_-|NUDIX-domain-containing-protein
MAREVKPWRRLRRGLEHDFSVAQVREDWWADPRTGHEHPRVRVDCADWVNVIAVTPDAQLVLVRQFRFGVEASTLELPGGIVEPGEAPERAAARELEEETGYVPGRMVPVGQVHPNPAFQGNVCFNFLALDCVKRHEGRQDAGEDIAVELHPRADLPRLILEGHISHSLVVAAFFQERLLSESK

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_7

3414393-3414617

Orphan

Consensus_repeat	Method
GGCGGGTGCTCCGGTGCC	CRT

4 spacers

The CRISPR arrays of NZ_CP017172_7

>merge|NZ_CP017172|7|3414393-3414617|CRT
GGCGGGTGCTCCGGTGCCACCAGGGCTGATGGGAGCACCGCCTCCGGCGGCGGGTGCTCCGGTGCCTTCGGGGATCATGGGCGCAAATCCTCCTGCGAAGGTTGGAGCGGGTGCTCCGGGGCTGATGGGCGGGCAGGCTCCTGCGACGGCTGGGGCGGGTGCTCCGGTGCCTCCGGGAATGACGGGGCATCGGCCTCCGTCCGCGACGGGGCTGCCTGCGGTGTC

>NZ_CP017172|7|1|3414393-3414617|CRT
GGCGGGTGCTCCGGTGCC	ACCAGGGCTGATGGGAGCACCGCCTCCGGC
GGCGGGTGCTCCGGTGCC	TTCGGGGATCATGGGCGCAAATCCTCCTGCGAAGGTTGG
AGCGGGTGCTCCGGGGCT	GATGGGCGGGCAGGCTCCTGCGACGGCTGG
GGCGGGTGCTCCGGTGCC	TCCGGGAATGACGGGGCATCGGCCTCCGTCCGCGAC
GGGGCTGCCTGCGGTGTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140796455.1\|3426443_3426938_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP017172.1\|WP_140874665.1\|3429243_3430524_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017172.1\|WP_140874651.1\|3398782_3401620_+\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP017172.1\|WP_140790535.1\|3409015_3410410_+\|undecaprenyl-phosphate-glucose-phosphotransferase	unknown	unknown	gnl\|CDD\|274396
NZ_CP017172.1\|WP_140874663.1\|3426934_3427807_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140854272.1\|3427803_3429036_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140874655.1\|3407651_3408797_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340833
NZ_CP017172.1\|WP_140798151.1\|3401621_3402887_+\|phosphoribosylamine--glycine-ligase	unknown	unknown	gnl\|CDD\|234856
NZ_CP017172.1\|WP_140790541.1\|3419310_3422103_-\|vitamin-B12-dependent-ribonucleotide-reductase	unknown	unknown	gnl\|CDD\|235828
NZ_CP017172.1\|WP_140798152.1\|3403992_3405108_+\|LptF/LptG-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP017172.1\|WP_140874659.1\|3423204_3425004_+\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|119365
NZ_CP017172.1\|WP_140790554.1\|3432719_3434033_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017172.1\|WP_140790537.1\|3410478_3412416_-\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP017172.1\|WP_140790526.1\|3402883_3403996_+\|LptF/LptG-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP017172.1\|WP_140854276.1\|3430849_3432157_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097
NZ_CP017172.1\|WP_140798153.1\|3405109_3406435_+\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP017172.1\|WP_140874653.1\|3406431_3407595_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340838
NZ_CP017172.1\|WP_140790542.1\|3422707_3423049_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP017172.1\|WP_140874661.1\|3425100_3426300_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140798149.1\|3397234_3398779_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl\|CDD\|234854

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140796455.1\|3426443_3426938_+\|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_CP017172.1\|WP_140874651.1\|3398782_3401620_+\|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.	5.26048e-21
NZ_CP017172.1\|WP_140790535.1\|3409015_3410410_+\|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_CP017172.1\|WP_140874663.1\|3426934_3427807_+\|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.	4.69434e-06
NZ_CP017172.1\|WP_140790554.1\|3432719_3434033_+\|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).	0.000136586
NZ_CP017172.1\|WP_140874655.1\|3407651_3408797_+\|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.	1.6697e-147
NZ_CP017172.1\|WP_140798151.1\|3401621_3402887_+\|phosphoribosylamine--glycine-ligase	gnl\|CDD\|234856	PRK00885, PRK00885, phosphoribosylamine--glycine ligase; Provisional.	0
NZ_CP017172.1\|WP_140790541.1\|3419310_3422103_-\|vitamin-B12-dependent-ribonucleotide-reductase	gnl\|CDD\|235828	PRK06556, PRK06556, vitamin B12-dependent ribonucleotide reductase; Validated.	0
NZ_CP017172.1\|WP_140798152.1\|3403992_3405108_+\|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_CP017172.1\|WP_140874659.1\|3423204_3425004_+\|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.	4.58879e-141
NZ_CP017172.1\|WP_140790537.1\|3410478_3412416_-\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	1.36151e-16
NZ_CP017172.1\|WP_140790526.1\|3402883_3403996_+\|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_CP017172.1\|WP_140854276.1\|3430849_3432157_+\|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_CP017172.1\|WP_140798153.1\|3405109_3406435_+\|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_CP017172.1\|WP_140874653.1\|3406431_3407595_-\|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.	4.9764e-81
NZ_CP017172.1\|WP_140790542.1\|3422707_3423049_+\|(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_CP017172.1\|WP_140874665.1\|3429243_3430524_+\|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).	0.000212132
NZ_CP017172.1\|WP_140798149.1\|3397234_3398779_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl\|CDD\|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0

>NZ_CP017172.1|WP_140790537.1|3410478_3412416_-|trypsin-like-peptidase-domain-containing-protein
MKRIPLACLVTALATGAPAALASDEVCQQEEVSSSSQRLTKVGEDVFRRFETTHPYATTQIRASDGPIHTDVITHAGAAYIAPHFERLDLEDGDFVVVRSPDNSRSWRYDNSHPGARSGFWAIHIAGETAIIELHSRDSVNRRGILNKHGYSIDRYARGYTNEEMGLSNDKALCGPDDTQWAPCYASSDPTLYGRARPVARLLINGSGACTGWLVGSQGHLMTNQHCVGTASEAQNTQYEFMAEGASCSTSCASWFGCPGNVIPGGTLVKVDAPRDYALIQLSQNPVNTYGYLQLRSSGAVVNERIYLPQHPAGHGKKIAVRSTDARDESGFAEIYSRNEASCQSGGPNDIGYYADTQGGSSGSPVIGHSDNLVVALHHCANCPNRGVPIEAVISHLGTSLPQCALPAADCPNPGGNGEPPPPPPPPPPPPENSFDYSASNTNSAQQNTTNHTIALTAGQTLTVATCGLTGTQFTGDTWLRLRNPAGTEVATNDDSCGGRGSSITFTAATAGNHEVLAGCYSSGSCTGRVVWEITGGSGSPTSGSFNFSGSNTNSAQQNTTNRDVAIAAGKSITVATCGVTGATFTGDTYLRLFNGTTQAAVNDDSCGGTGSSLTYTSPTATTLQIRAGCYSSGNCTGTVVWNIQ
>NZ_CP017172.1|WP_140790535.1|3409015_3410410_+|undecaprenyl-phosphate-glucose-phosphotransferase
MFSRLQRFYTSIKVVADMVMLALAFVLAYATRFSGIVPVTEGIPPWTDSFFSLLMVLVIFPVTFHQSRLYGTNRSRTNTGEVFEVFKSTITAALILVAVTYFVRERYSRLTLVIFIVYAFALVTCSRLVTRYLVSEIRRRGHNLKSILVIGAGDLGQRVIETVEHHRELGFRVMGVLTLHPEKVGQYVNDVRVIGLVDQVNEVLDSHPVDQVILALPLEGHAHVKALMDKLALRTVDVRVVPDLYQYITLYGGLEEFGGLPIIRLQGDPMEGWSRVAKRAFDILFSLLAILITAPLMAATALAVRLTSRGPMLYRQERMGMDGRTFPILKFRTMRIDAEHSGAMMACPDDPRRTVIGTFLRKYSLDELPQFFNVLRGDMSLVGPRPERPVFIEEFKRQIPRYHLRHKVKAGITGWAQINGLRGQTCIEKRIEYDLYYIENWSLLMDLKILVRTALGGFLSKNAY
>NZ_CP017172.1|WP_140874655.1|3407651_3408797_+|glycosyltransferase
MKVALVHDWLVTHRGGERVLDALCEVLPDADIYTLIHKPGSQSPAIESRRIFTSFLQHIPGIHARYRHFLPLMPKAIESLQLQGKYDLVLSSSHCVAKGLRTPRGTPHLSYVHAPMRYMWDLFDDYFGPGRTGLPVRAAAHAIRPWLRRWDRRTAAGVDRFIANSRHIATKVQRFWGREASVIHPPVSLERFAQVPLEGGGQGGYFLWLGAFAPYKRLDVALEAFRNLDAQLWVVGTGQEAARLGARSLPENIRFLGNVLDASLPALYRDARALIFTPEEDFGITPLESQAAGRPVIAYGKGGALETVTAQTGMFFSEQTPESLAAAVRRFDEWEAGFRPEAARAQAERFGRAHFQSAILREIHSVLGDVLPDSPGPAAGL
>NZ_CP017172.1|WP_140874653.1|3406431_3407595_-|glycosyltransferase
MPARPPWRPRVWYAEAVAHVLLDLRMVRGRLHGIARYALELARRMPVLAPDLRFSALVPPEGLAPDLGELTPRMPLHRALAGFLSPLEQPALAADLVKLAPDAFHATSFSLPLFWNGRLVATLHDANHLALADQYTPAQSIYYRVVVGPRAKRATALVTVSEFSRDELAKHLKLSPYRLQVIHNGVDARFQPPTQAEAAAFRERYELPARYVAAVGNAKRFKNLALLKDFAGELPVPVVLLAGKGAVAHELGLHENVFDLEELPEDQMPLFYGAASALLLPSRYEGFGLPALEAMGAGCPVLASDATALPEVVGNAALRLFPDDAAAWREATLRVLRDDVLRRELVELGRERVARFTWDDCARRTLAVYRRVLEAPAPGGSRGTPPR
>NZ_CP017172.1|WP_140798153.1|3405109_3406435_+|O-antigen-ligase-family-protein
MSAHMGTASELPLDLRWRRAINAVLVLWTVGLVLAEVVLQVATGAAVLLAAILLVRGRLRLAPDVRAYVGASGVLCLWQAASPAVALLTGAAESWPRGSRYGQVLDSVAGAAAACIGAVGVPWLLLAGVLAGGWLLAALLGVFQNRVRWSMELPSFLKLNLGRLHENFGTEESPRYAAGGFFSHRLRFAHGAIAALGPALSVLGIADQARRRVLAGAVVMGMLISIYNAFARAALGAALLVSVVALLLLVQGSARKMGLALLFALVAVVSMSPAWRTRLEKAVGNIYGGEREHAMAVGWSLVREYPLTGVGFGNHKPAALATQDETGITDLLATDSHNLWLTVWAETGLVGLLLTLAMHALLGRALIRRYREGSIAATGALLSWVGFHILALVHYLPFHSSVYLSFSLIWGLGLCEGSERLRGREARQGLLEVEGAPRPSP
>NZ_CP017172.1|WP_140798152.1|3403992_3405108_+|LptF/LptG-family-permease
MRGTLFIYVLRTYLRFALGILGGLVLVFVVVDFVDRAKLYTGPGWVWDVAELYFYKAMMSVQQLGPAALLLAAGTTVSALRKQGEVTAIRALTFGPSALYLPILVASFVACVGLVAFDERVATYSGRRVDEITTQRFNKWGDWRFYYTPKQWFRRGDNIFFLRGGSAQEGFQDVSVFTVTESFDLQRRLDASGMFPVEGMRWRLTDVVERTFDGEGKTSVRQLPEAEYELGVAVTAFRIRPGRPEQMRASELREQIVARRDVGLATKQFELALHNRFAYPMAAFPAALLGVGLALRTNRRGHLTAAIIEGLLTAVAMWGLMMVCRTLVLTERLSPGVAAWTPTVLLGLIAGAVWLQREGRLHLPRRSLLVR
>NZ_CP017172.1|WP_140790526.1|3402883_3403996_+|LptF/LptG-family-permease
MNRLSRYLLGELLVPLGVWVAFMFLLLFVMQFLRGTDVLLGSSVTLVDMARLLAYLAPHFLMMALPIAFLLAILLGLGRLGEDRELVALQALGIGPVRLLAAPMGIAVALSVLMLVITSTAQPWGLAGLKVLVSEVIRKNAVGDVKSGVFYEDLSNLTLYAEQVSADGKWTNVLLHDDREANSPLLVLAQRGQVGTSTSGEVLRFALEAGEVHRSAGRETEEYSIIRFDQAEISVGVGASMGKRSRFSFSREELTPGELLEAAREAEAQGEDARMYRMALHSRLGNALAPIAFALLGTPLAMGRRQSGRAWGYLLTLGGYVLYYLLSRVFEQMGQKGQLPVGLAGQMANLVFVAVGLVALYRVSRSGTVK
>NZ_CP017172.1|WP_140798151.1|3401621_3402887_+|phosphoribosylamine--glycine-ligase
MDVKVLLLGSGGREHALAWKLSQSPLLTQLLCGPGNPGTAKLGTNVALRADVPEEVAAFAKREAVDLVVVGPEAPLVAGVADALADAGIACFGPVAEGARIEGSKAFAKEIMAEAGVPTAAFQTFTDVAAAEAYAVEQGRIVVKADGLAAGKGVIVAHDVEAARAAVRAVGAMGAAGQTMVLEELLEGEEVSAMALCDGERYAMLPLSQDHKRVGEGDTGPNTGGMGAYSPAPFLSAAQLAEVGERVVAPTLAVLRRRGIPFRGVLYAGLMLTRGGPKVLEFNARFGDPETQVLMMQLGEDLLPLLDACARGTLTPRTLVSSPGASVGVVLAARGYPDAPEKGQRIEGLDAVPPDATVFLAGVEARDGGVVTAGGRVLTVCARGEDLAQARERAYAAAAAVRFEGMHFRRDIGARGMKAAP
>NZ_CP017172.1|WP_140874651.1|3398782_3401620_+|zinc-ribbon-domain-containing-protein
MRIVCQKCAAAYAIDDKLITAKGVRAQCPRCRNLQLVRRDPSAVPAAGAPAPASQPAAPVTLTPVSGAAPADDLFGDFGAPPPAAPAPGAAPAPKPARGERAPGSELFGDFGAMPSPAPASAPPVDPFAGLGTPASGGGGAGAEDPLLDFLGPPPSAPQGMESQPSRPAKPAAAKPATSGCRVCQKPLTDSFDQALGICDDCRQPGSAQAPAAASRPAAPAGNSDFLPAMADLGGGSASVAQASEPEPGAESRSGARVPISTDIIPDMGPEPRSGIRASSPQLGAEPRSGSRSAPVRVTDGRSRGGKGGLVAGLVGLVVVGGGVGGYFLYQQQQEASRRQAGPPPAAAIPDAVQAVLPRWKLKYLEIPGTSAERLAQGQQQLARDERFAYAEAEESFQQALVLDPTSDAAIAGYVQALALGRGARMDDVTFQEARALLSAAESRSGRTAPLLLAHANLLLARSGQPEQARPLAEELLARAELPDAQKAEAHLVLGRTWLSSSRELARSHFDSAQKLSPDIKRLHYYRALAHVSGGEYSAALDTLRKRLETSPKDWESLALTARIYQEVGEPAEARKLYEARVKAEPGELRALLPLAMLRYQAEGNAAGAVRDLRALMKNRARYDEPEVAEVLVHLAAAERTAGSQDAAVKSAEEALQLVKELPEAHLQLFLVGLSRRDAEKARTHLAGFRGQLEDGALEKVLEGRLLLLEKKPLEALEAFQEAVKLDARRLDAQLLAGVAAASAKRRDDAFRALHQALQSDPLRLEPRPATSAYWLRPRETVEGVEGAILALSEGPEDPSPLLYEGLLRFHQHQFDAAERHLRSVLEVDANNAGALAYRALIALQRGATADARRLGERSAAAGRQMPVSHLAHGLALAEARQVEPAKRALRDALALAPTLLSAQAQLAQLESARGKDVARDTLVKVVGLDPAYLPAKRMLYLLER
>NZ_CP017172.1|WP_140798149.1|3397234_3398779_+|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MLALLSVSDKRGLVPFAQGLVRLGFRLLSTGGTLEALKGAGVPVTKVSEHTQSPEILGGRVKTLHPRIHGGILGRLELEADREEMKAHGIEPISLVAVNLYPFRQTVASGAAEPEVIEQIDIGGPAMVRASAKNFRHVSVVVDPDDYPAVLAELEQQKAVSEDTRRRLMRKAFAHTAAYDASISAWLSAQAGEPFPGELSLAFRKSQELRYGENPHQRGAFYREHAAPQEPTVAFAKVLQGKELSYNNILDLDAALGLLLEFPEAPAAVIIKHNTPCGVAVDDALVKAYRTARAVDEVSAFGGIVALNREVDAATAQAMAETFLEAVIAPSYSPEALQVLAAKKNLRLLEAGPALASPQARPRAQLDARSVSGGMLLMDRDSVEPPLSWKVVSKRVPTPEEERAMRFAWKVCKHVKSNAIVFASGDQLLAQGGGQTNRVDSVRIAMQRGGAALRGSAVASDAFFPFRDGLDEAARAGATCVVQPGGSVRDAELIAAADEHGMAMVLTGVRHFRH
>NZ_CP017172.1|WP_140790541.1|3419310_3422103_-|vitamin-B12-dependent-ribonucleotide-reductase
MDKELSSKSTVNGKERRGGRKARVAATGLTVERFFTTPGVDPADELAWEYRSASITGEDGKAVFEQKNIEVPKSWSMLATNVVASKYFRGTPGTPERETSVRKLVARVVDTLTRWGVEGGYFTRDADREAFHAELTHLLLRQKASFNSPVWFNVGVEAQPQCSACFINSVEDNMDSILTLARTEGMLFKYGSGTGSNLSTIRGSKELLAGGGTASGPVSFMRGFDAFAGVIKSGGKTRRAAKMVILNAEHPDILEFIRCKSTEEKKAWALIEAGYDPSFNGEAYSSVFFQNSNNSVRVTDAFMKAVVDDATWTTRSVRDGQPLDTYQARELFREISEAAHLCGDPGMQFDTTVNSWHTCSTTARINASNPCSEYMFLDDSACNLASLNLMHFRTIDGDFDVTAFRHAVDILLMAQEIIVGNSRYPTERIEKNSHDYRPLGLGYANLGALLMASGLPYDSPAGRNYAGAITSLMCGEAYAMSARLAEKQGPFAGYAKNAEPMLGVIRKHRKAAYHIAPEGVSQGLFAAQKDAWDRALALGEEHGFRNSQVTVLAPTGTIGFMMDCDTTGIEPDIALIKYKKLVGGGMLKIVNQTVPLALEKLGYPQTQSQDIISYLDKQDTIEGAPHLKPEHLPVFDCAFKPAQGERSIHWMGHIQMMEACQPFLSGAISKTVNMPSDATVEDIEKAYLEAWKRGLKAIAVYRDGCKRTQPLNTSKETVKDTRAAKSTVAPEPAPAVQPEPRAVRRRLPDERRSITHKFSIGGHEGYLTVGMYEDGLPGELFIVMAKEGSVVSGLMDSFATSVSLALQYGVPLKVLVDKLSHTRFEPSGFTGNPDIPIAKSITDYIFRWLELKFLPSEEEDAVLDRVDVQPKREALPAQTASVQRSDSNSSKRSTWLNQADAPPCHTCGAIMVRSGACYKCGNCGATSGCS
>NZ_CP017172.1|WP_140790542.1|3422707_3423049_+|(2Fe-2S)-ferredoxin-domain-containing-protein
MAPPYQRHVFVCTNRRPDGNPKGCCASKGAEEVRAAFKAELDKRGLKGHMRANAAGCLDTCSFGVAVVVYPEGTWYGGVQVEDVKDIVEQHLMEGRPVERLLMPFSRKAVTPG
>NZ_CP017172.1|WP_140874659.1|3423204_3425004_+|glycosyl-hydrolase
MRRSWWASGLIATALSVAGCDSEVPSSHVRDLMAFQDAALAAEWSVGVAYSVGTRVTYQGRLYECRQPHTSQADWTPVAVAALWLDLGPAGGGEPDAGSGGTDAGTGGDVTAPTVGLSASTSRIIAAGPLSLTATATDDVGVTRVEILENGTVVATGSQFSRAFSGWEQNGTYVYAVRAHDAAGNVGTTTLTVVVDIPGGPPPGGKRIVGYFTAWGIYARNYHVSNVQPSKLTHINYAFSNISGDGRCILGDPFADIDKGGGWQGEWDPGQLRGNFRAFKEMKRQNPHLKLLISVGGWSWSTHFSTVASSPASRAAFVKSCVDLYIRGQYPGVDPVNGEGVFDGIDIDWEYPVGGGLPGNSNSPADKQNYTLLMQEFRSQLNAVTTQTGKPYLLTIATGASPDLLENKQETKKLSDVLDWINVMSYDYHGAFESTVNFHSALNRVTGDPGAATGFYTDGSVSKMLALGVPPAKIVVGVPFYGRGWGSVPNVNNGLFQSGVPTRGTWDDGSSGLTGVFDFKDIKANYERAGSGYTKFFHPEAKQAYVYNPATGIWIGYDDVQSMNAKADYILNKNLGGAMFWELSGDDGSLLDALARKLR
>NZ_CP017172.1|WP_140874661.1|3425100_3426300_+|hypothetical-protein
MSFAAAVLLVALSSSSLAAEPWTAVVRVASDEDTALLVRVRGQSSDLPIRLEVSSGAPLEGFREGPWLAAERLAGRHQARAVLWFVREGSDVRVQVAEFDSRRLFSRAARLGQSPGSLEWSTGAEALALAARSALRAVEAGAPLGDVVEVAPPRHASNEEGTETGVGRRIGEASSGDEAAPRTPTSPSPEEAIALAEDGALASARECVASPREGLGLASAEENPARQMWLALGGHAALDGYTRRGHQGLVVGVGLQPGRWRLRAQVLASVPTRLRDARTELTLGQHAASVWAGLPWAAAEGLDVEAGFGAGAVVFTRRTQALTEDVKAAPPGTMLALLMGPELRTRWRMGARVGLETSLAAEVLLGRPELRYAIDGNFVSRGAGWAVRPRLGLAMVVFL
>NZ_CP017172.1|WP_140796455.1|3426443_3426938_+|sigma-70-family-RNA-polymerase-sigma-factor
MLMELLPRVRNLVRYLVRGDVDVEDIAQEALIALVRGLPSYRAEGRFQSWADRVVARTAFAWLKRSRGRDAQHADAPVELVAVPSEDALPDEYVHRRHMVTLLDRLSTEQRHALVLHHVLELSVPEISTELGIPFETVRSRLRLGRTALRSLASAEGDGGEERG
>NZ_CP017172.1|WP_140874663.1|3426934_3427807_+|tetratricopeptide-repeat-protein
MSDFREEGDDALNALVLPLDEGAGPARRISRERSAQMVLAALEAGALVSQPTPRPRGKRPPVWLMTGALLVAGAAAAAVWSFTRSSRASTSQVEEAVLTIPPRLGTASQRSDTEAVDTAPSRLDAVSEVVPAETPAVPAAFIAEAEGASEPVRPRAPPATVKSAAPEDLLLKANGLRSDGRWKEAEALYLRVIRAEPSSLASYVARVASGSLRLEHLGDARGALRQFKAALRIQPRGVLDQEAQHGIAEAHRVLGNRDAERSALESFLSTHPDSPLVPSARARVRELTAP
>NZ_CP017172.1|WP_140854272.1|3427803_3429036_+|hypothetical-protein
MNRRWTLAVLLAASMGSCTRGDLVATVQSPDAGHVGSSADAGGPDGGEPPDDWEAYCAGRGPPIVVGDAYTDSQVCSGRLAERTFRHALCTCEGLALGASFETDAFHGTTGTYQPGGAGGDVGVNGALSANDAVSVGGSLSIGGAGGAQLGQTFRVGDALHCGGPLTGNPVSATVVGDARVRGDVALPAFGVGGVLTVPAGHVLGPVDAAEVRREPVDPVIPCSCDAASQVDVSGLIARHVLDNDNAAIGLDATAMEDIEGERALELPCGRFHLTRITGTGRATITIRARTGLFIEDVVDLGEGLSVDVHAPGELDLFLGGAVAVAGPLTLGSTATPSRVRVYVAGSNVLALSAGSTLAGNLYAPRAALSLSGGAEVFGSVFVRQVEASGPLRLHYDADIRDAGAECTGD
>NZ_CP017172.1|WP_140874665.1|3429243_3430524_+|hypothetical-protein
MKREVKAGIAGLVFGSMLVGCGVAPEQGELGGVEDVTAGASASAETGLDAHRGSSTPVAVARYGHAVAYGDGKYFAVWADVRTGGIYGTRVKPDGTVLDPGGIRINFGEEIGKRPAIAFNGTHFFVVWGTINGVDGVRVKPDGTVVGPMFRAVQSDEVFDPARVACSPKICLVTYTVAGDDSSTIYFTRVSKDGVILSTADRTLSASNTFADDASSTWNNSKKEFLAVWSVEQGDGPENADIYGNRVKEDGTILDGSGFPISAAEGAQTTPDVVWTGKSYQVVWSDDRNGNPDIYGARVSKTGTVKDPDGIPISTEVGAQTAPRIAHHNSKSLVVWDDTRYGPHSIWGARWGEDGDVWDGSGFPISSAGLAQQYLPDVAFGADKFFTIYAAQETYSPGDPHYIVGTRVTHQAQVNDVPAVPLTRRR
>NZ_CP017172.1|WP_140854276.1|3430849_3432157_+|hypothetical-protein
MFFKGRSHMNREVKAGIAGLLFGSMLAGCGVAPEQEWQGGVEDATAEAEALMSVETGPEEHRSRARPAALAKFGPAVAYGDGKYFTVWTDVRIGGIYGTRVKPDGTVLDKEGIRINIGDVEGFRPGIAFNGTHFFVVWESVDGIDAVRVKPDGTVVGPVFNVKQSGETVGPARVACSPKICLVTYTVSGDFSNIFFTRVTKDGVVLDTGDESLSASDTFANDASPTWNNKTKEFLVVWSDEHGEGPENADIYGNRVKEDGTILDGDGFPISQAEGAQTTPDVEWTHKNYQVVWTDDRNGNPDIFGARVSKTGMVKDPEGIPISTEEGAQAEPRLAHHNDKSLVVWDDTRDGPHRVWGARWGEDGDVRDPSGFPISTGDQPQEYLPDVAYGGGKFFVVYSGQETFEPLEPHFILGTRVTHQAEVKDVPALTLTRQR
>NZ_CP017172.1|WP_140790554.1|3432719_3434033_+|hypothetical-protein
MFLKGRLHMRREVKAGIAGLLFGSMLVGCGVAPEQEELGGVEDVTAESEAEAQMSAETGPEERRGYANPAPLARYWPAVAYGGGKFLAVWTDVRTGGIYGTRVKPNGTVLDKEDIRINIGDVEGFRPGIGFNGTHFFVVWESLNGVDAVRVKPDGTVVGPVFNVIQTGESVGPVRVACSPKICLVTYTISGDFSNIYFTRVTKEGVVLDTADQTLSASDTFANDASPTWNNKTKEFLVVWSDEHGEGPENADIYGNRVKEDGTILDGDGFPISQAEGAQTTPDVEWTHKNYQVVWTDERNGNPDIFGARVSKTGMVKDPEGIPISTAEGAQAEPRLAHHNDKSLVVWDDRRDGPHAVWGARWGENGDVWDPSGFPISTGDQPQEYLPDVAYGGGKFFVVYSGQETFDPLEPHFILGTRVTHQAEVKDVPALPLTRQR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_8

4135497-4135607

Orphan

Consensus_repeat	Method
TGGCGCAGTTCCCACGGCGAGCAACGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_8

>merge|NZ_CP017172|8|4135497-4135607|CRISPRCasFinder
TGGCGCAGTTCCCACGGCGAGCAACGCCACTCAGACCTTCGGGGCAGCGCCCCCAGTAGCCCCCGTGGGCGTGACGCAGGCTCCTGGCGCAGTTCCCACGGCGAGCAACGC

>NZ_CP017172|8|7|4135497-4135607|CRISPRCasFinder
TGGCGCAGTTCCCACGGCGAGCAACGC	CACTCAGACCTTCGGGGCAGCGCCCCCAGTAGCCCCCGTGGGCGTGACGCAGGCTCC
TGGCGCAGTTCCCACGGCGAGCAACGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140875055.1\|4134636_4135053_+\|helix-hairpin-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378965
NZ_CP017172.1\|WP_140791447.1\|4145306_4145732_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225794
NZ_CP017172.1\|WP_140798401.1\|4128298_4129405_+\|fatty-acid-desaturase	unknown	unknown	gnl\|CDD\|239583
NZ_CP017172.1\|WP_140791449.1\|4145744_4146014_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140791431.1\|4131692_4133219_-\|histidine-ammonia-lyase	unknown	unknown	gnl\|CDD\|236484
NZ_CP017172.1\|WP_140878358.1\|4135157_4135436_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140875053.1\|4129417_4130281_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|369777
NZ_CP017172.1\|WP_140875051.1\|4121527_4128274_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|238429
NZ_CP017172.1\|WP_140878360.1\|4136496_4137420_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_162521043.1\|4136153_4136327_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259287.1\|4118748_4119864_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP017172.1\|WP_140875059.1\|4139686_4141462_+\|HEAT-repeat-domain-containing-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140791445.1\|4143675_4145298_+\|Hsp70-family-protein	unknown	unknown	gnl\|CDD\|234715
NZ_CP017172.1\|WP_174259288.1\|4130404_4131559_+\|DUF839-domain-containing-protein	unknown	unknown	gnl\|CDD\|253386
NZ_CP017172.1\|WP_140875061.1\|4141506_4143585_+\|UvrD-helicase-domain-containing-protein	unknown	unknown	gnl\|CDD\|223288
NZ_CP017172.1\|WP_140875063.1\|4146323_4147283_-\|TerC/Alx-family-metal-homeostasis-membrane-protein	unknown	unknown	gnl\|CDD\|274743
NZ_CP017172.1\|WP_140791437.1\|4137586_4138768_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133061
NZ_CP017172.1\|WP_140791433.1\|4133354_4134632_+\|aspartate-kinase	unknown	unknown	gnl\|CDD\|235843
NZ_CP017172.1\|WP_140798399.1\|4119998_4121504_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187617
NZ_CP017172.1\|WP_140875057.1\|4138786_4139635_-\|CHAP-domain-containing-protein	unknown	unknown	gnl\|CDD\|377495

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140875055.1\|4134636_4135053_+\|helix-hairpin-helix-domain-containing-protein	gnl\|CDD\|378965	pfam12836, HHH_3, Helix-hairpin-helix motif. The HhH domain is a short DNA-binding domain.	2.90662e-15
NZ_CP017172.1\|WP_140791447.1\|4145306_4145732_+\|hypothetical-protein	gnl\|CDD\|225794	COG3255, COG3255, Putative sterol carrier protein [Lipid metabolism].	5.43621e-06
NZ_CP017172.1\|WP_140798401.1\|4128298_4129405_+\|fatty-acid-desaturase	gnl\|CDD\|239583	cd03506, Delta6-FADS-like, The Delta6 Fatty Acid Desaturase (Delta6-FADS)-like CD includes the integral-membrane enzymes: delta-4, delta-5, delta-6, delta-8, delta-8-sphingolipid, and delta-11 desaturases found in vertebrates, higher plants, fungi, and bacteria. These desaturases are required for the synthesis of highly unsaturated fatty acids (HUFAs), which are mainly esterified into phospholipids and contribute to maintaining membrane fluidity. While HUFAs may be required for cold tolerance in bacteria, plants and fish, the primary role of HUFAs in mammals is cell signaling. These enzymes are described as front-end desaturases because they introduce a double bond between the pre-exiting double bond and the carboxyl (front) end of the fatty acid. Various substrates are involved, with both acyl-coenzyme A (CoA) and acyl-lipid desaturases present in this CD. Acyl-lipid desaturases are localized in the membranes of cyanobacterial thylakoid, plant endoplasmic reticulum (ER), and plastid; and acyl-CoA desaturases are present in ER membrane. ER-bound plant acyl-lipid desaturases and acyl-CoA desaturases require cytochrome b5 as an electron donor. Most of the eukaryotic desaturase domains have an adjacent N-terminal cytochrome b5-like domain. This domain family has extensive hydrophobic regions that would be capable of spanning the membrane bilayer at least twice. Comparison of sequences also reveals the existence of three regions of conserved histidine cluster motifs that contain the residues: HXXXH, HXX(X)HH, and Q/HXXHH. These histidine residues are reported to be catalytically essential and proposed to be the ligands for the iron atoms contained within the homolog, stearoyl CoA desaturase.	6.74355e-23
NZ_CP017172.1\|WP_140791431.1\|4131692_4133219_-\|histidine-ammonia-lyase	gnl\|CDD\|236484	PRK09367, PRK09367, histidine ammonia-lyase; Provisional.	0
NZ_CP017172.1\|WP_140875053.1\|4129417_4130281_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.5756e-22
NZ_CP017172.1\|WP_140875051.1\|4121527_4128274_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|238429	cd00833, PKS, polyketide synthases (PKSs) polymerize simple fatty acids into a large variety of different products, called polyketides, by successive decarboxylating Claisen condensations. PKSs can be divided into 2 groups, modular type I PKSs consisting of one or more large multifunctional proteins and iterative type II PKSs, complexes of several monofunctional subunits.	3.14464e-101
NZ_CP017172.1\|WP_140875057.1\|4138786_4139635_-\|CHAP-domain-containing-protein	gnl\|CDD\|377495	pfam05257, CHAP, CHAP domain. This domain corresponds to an amidase function. Many of these proteins are involved in cell wall metabolism of bacteria. This domain is found at the N-terminus of Escherichia coli gss, where it functions as a glutathionylspermidine amidase EC:3.5.1.78. This domain is found to be the catalytic domain of PlyCA. CHAP is the amidase domain of bifunctional Escherichia coli glutathionylspermidine synthetase/amidase, and it catalyzes the hydrolysis of Gsp (glutathionylspermidine) into glutathione and spermidine.	3.4909e-05
NZ_CP017172.1\|WP_174259287.1\|4118748_4119864_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.40974e-71
NZ_CP017172.1\|WP_140791445.1\|4143675_4145298_+\|Hsp70-family-protein	gnl\|CDD\|234715	PRK00290, dnaK, molecular chaperone DnaK; Provisional.	2.28129e-172
NZ_CP017172.1\|WP_174259288.1\|4130404_4131559_+\|DUF839-domain-containing-protein	gnl\|CDD\|253386	pfam05787, DUF839, Bacterial protein of unknown function (DUF839). This family consists of several bacterial proteins of unknown function that contain a predicted beta-propeller repeats.	3.74397e-27
NZ_CP017172.1\|WP_140875061.1\|4141506_4143585_+\|UvrD-helicase-domain-containing-protein	gnl\|CDD\|223288	COG0210, UvrD, Superfamily I DNA and RNA helicases [DNA replication, recombination, and repair].	5.61848e-157
NZ_CP017172.1\|WP_140875063.1\|4146323_4147283_-\|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.	6.8525e-159
NZ_CP017172.1\|WP_140798399.1\|4119998_4121504_+\|SDR-family-oxidoreductase	gnl\|CDD\|187617	cd05359, ChcA_like_SDR_c, 1-cyclohexenylcarbonyl_coenzyme A_reductase (ChcA)_like, classical (c) SDRs. This subgroup contains classical SDR proteins, including members identified as 1-cyclohexenylcarbonyl coenzyme A reductase. ChcA of Streptomyces collinus is implicated in the final reduction step of shikimic acid to ansatrienin. ChcA shows sequence similarity to the SDR family of NAD-binding proteins, but it lacks the conserved Tyr of the characteristic catalytic site. This subgroup also contains the NADH-dependent enoyl-[acyl-carrier-protein(ACP)] reductase FabL from Bacillus subtilis. This enzyme participates in bacterial fatty acid synthesis, in type II fatty-acid synthases and catalyzes the last step in each elongation cycle. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	8.8729e-66
NZ_CP017172.1\|WP_140791433.1\|4133354_4134632_+\|aspartate-kinase	gnl\|CDD\|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	0
NZ_CP017172.1\|WP_140791437.1\|4137586_4138768_+\|glycosyltransferase	gnl\|CDD\|133061	cd06439, CESA_like_1, CESA_like_1 is a member of the cellulose synthase (CESA) superfamily. This is a subfamily of cellulose synthase (CESA) superfamily. CESA superfamily includes a wide variety of glycosyltransferase family 2 enzymes that share the common characteristic of catalyzing the elongation of polysaccharide chains. The members of the superfamily include cellulose synthase catalytic subunit, chitin synthase, glucan biosynthesis protein and other families of CESA-like proteins.	2.58775e-117

>NZ_CP017172.1|WP_140878358.1|4135157_4135436_-|hypothetical-protein
MPAPCPFDATAPYDCVVPTGAPDEGACAERSAAPAPNTCVVVVTDEPAVAPGGVPAKSCVDFMLERAGPAPPVTAGVDREGGGAPCGAAMNT
>NZ_CP017172.1|WP_140875055.1|4134636_4135053_+|helix-hairpin-helix-domain-containing-protein
MASRTAALAAVALGVLGVGVVARLRWPDAAPALDCAAESVRIRPDGVALCGDGAVPTGAQALALGRPLDLNSATEEELALLPGVGRTLARSLVEAREEQGGFKSWDDVDAVRGVGAAKLQTLRAATALGAPPDAGPVW
>NZ_CP017172.1|WP_140791433.1|4133354_4134632_+|aspartate-kinase
MALIVQKYGGTSVGDVARIKNVALRCLAAQEAGHDVVVVVSAMSGETNRLLKLVAQLTDRPDEREQDVVVATGEQVSIGLLAMAIHAQQGKATSFLGHQVRIVTDSTFSKARIKSIDAQPIRAALARGHIVVVAGFQGVDESGSVTTLGRGGSDTTAVAVAAALNAHACEIYTDVDGVYTTDPNMVPSARKLDRITYEEMLELASVGAKVLQIRSVEFAMKYKVPLWVKSSFTDDPGTLVCEEDSSMEDVLVRGVAYDRNEAKITVCGVPDVAGAAAKIFGPLDEKHIVVDLIVQNPSKNGRTDLTFTVGKADFLTAQEVVRKVAEEIGASGIETDGDIAKVSIVGVGMRNHSGVAARMFQALSAEGINIQMISTSEIKVSCVVHAKYTELAVRALHTAFGLDQPMPPEGVSAVSETAALMGEKV
>NZ_CP017172.1|WP_140791431.1|4131692_4133219_-|histidine-ammonia-lyase
MSRPRILIDGDTLKLEEILQVARNEATVELSPDAATRVRASRALVDRVAAGDTPAYGINTGFGTLAEVRIDKKDLRDLQRNLILSHACGVGTPLPLPEARALLLLRCNVLAKGYSGIRMETLALALDMLNRDVVPVVPERGSVGASGDLAPLAHLALVFIGEGEAFHQGQRMPAKQALERAGLQPVVLEAKEGLALVNGTQAMCAVGTLLQLRAESLADIADVAGAMTLEGLLGSHKPFIPEIHDVRAHPGQKDVAAHLRRILVDSELVESHVNCSKVQDPYSLRCMPQVHGAAREGIAFSRRILEVEVNSATDNPLVFADTERIVSGGNFHGQPISLAMDVVAMALTQLSSISERRVEQLVNPSLSNLPAFLAKNSGLNSGFMIAQVTSAALVAESRVLSHPASVDSIPSSAGREDHVSMGMTAALKGRQVSDFARSCLAIEILVAAQALDFRLPLKPGKGALAAYELVRSKVPHMDKDRELHRDIEAVSQLVDSGELLAAVRSATA
>NZ_CP017172.1|WP_174259288.1|4130404_4131559_+|DUF839-domain-containing-protein
MQRRSFLRLTAMSSGLLVLGPGFWRSVYAAPARPGPGPYGAISGAPDAQGLRLPAGFSSRIIARTGQRVPGTHYTWHAAPDGGTCFPTDDGGWVYTSNCELPLIGGASSIRFDGGGNVTSAYRILEGTQLNCAGGPTPWGTWLSCEEWDGGHVWECNPQEPSQGQRRNALGTFAHEAVAVDPVGMRLYLTEDRPEGRFYRFTPAQWPSLSSGTLEAAKLNGSALDGTATFSWVRVSASLPAYLQLARFLTTAFDGGEGCWYDSGTIYFTTKGDNRVWAHTPATGTVELLYDDDLYPESPLRGVDNITVSRSGDLYVAEDGDDLQLCVFTPGPERSVAPFLQVVGHAGSELTGPAFSPDGQRLYFSSQRGTDGNGVTFEVRGPFR
>NZ_CP017172.1|WP_140875053.1|4129417_4130281_+|methyltransferase-domain-containing-protein
MLWGTMPPSDTESYLLDYHRRLAGVTARWFAKTPVIRGDSRFASTYELLAAEVPQDAPPRTVLDLACGDGYLLELLALRAPQCPGLVGLDMSEDELAQAQARLKGAATLIRGVAQSLPFEDASLDVVLSHLALMLMDDCEKVLSEIRRVLTPAGKLSCVVGGGFVPSGALAVFRALMKPAIEAQPRPLLSLGDTRFRSTEGLRALFDLAFERVEVFDLEVQEGGPPEQVWASLSTTYDADQLSPDAREDVRRAFLAAVEPMKDSTGNITCLWSMRQVTASAPRRRGV
>NZ_CP017172.1|WP_140798401.1|4128298_4129405_+|fatty-acid-desaturase
MNSSNPQAGPIPADDPRRLRSELRRVMPPESFQPQPLRGIVAFGLVPVMVVLMWAAGSGRLPWWACLLSSFALGQMVTAVGLAAHEALHHAVFRSRALESLLGWVGFSPFLVTPGNWRAWHVQAHHSAANVLVRDPDILPRQSEWRTQWFAKVFHAMSPGSGSLLSFVSFSFFFTAQGQAFLWHHSRLPQFKHVHMHRTRERILTVLVTLGWVAVGWWMGPMGALYALILPLLIGNITLMIYIATNHWLLAAHEESDNPFVNTASVATHPVMDWLHYNFSHHQEHHIFPAMSPKFAPLLRKHLRELNPEASQVYPHLHALRMLYRRPALYAEDGQTLMAPEGTPSISTEALRSQLKGGDSSLEHGLPR
>NZ_CP017172.1|WP_140875051.1|4121527_4128274_+|SDR-family-NAD(P)-dependent-oxidoreductase
MGYFAVPYDIHFDDTMAYGSHHFLTNFKFQCAGREHLLFSPDVFDVPEFRRDFDQVLLLTYEGYSRNLAPANLGDRLVVLTTLEERGEVSIRFCFRTLKSDGTPVACGFQTVLCADRTSGALCSFPKSFLRCFDSLSGIFERAGARSFRDCVQKGGSALKDVFPESIRALAKSLLADPASLGASRVVSLEGAPAARTAESPDALVLPQGATAFLFAGQGSFEPGLYLQLKALDPDLGDELQGVAAACRAVGVEAEPLLAARDVSDVRRALEQLPQLDQLGIYLSGVLGARWMQRQGASPDVFVGHSFGEIAAMAAAGALDLRAGAQVVCQRIRALQVLPDDFGTLAAVALGESEAVRAIAECGASGLHIAGRNHARQTVVAGARGQLARLRALLEGRGQGFTFVSSRYPFHHPDMAPAAKSFREMLGRVPMQAPRGRVYSPIERRAYVGGQPELADALASHLVRSFDFLGTVETLSRAGCTRFVDCGTTGVLARIVQKIIPAETAAEVSVISNLLPAERSAPSAGIEPKSVEAAAVDDSGIAVVSLGCILPGGAKDPETYWQNIRKGISGIVDQGLLQPELVTDFAGPAGTPDRTYTLLTGHVRDEDLVAPPGFDPTRFQQYVREQKLLAIALSQAMQGLKPVASKSPGRIQCLLGSTAEGSAEYDAALSVEAGEALLSARGERGHDVAALASAAREALGVEAISRDLAPHPTLQAVVTDVVGQGVATTLLDAACASSLYAMALGMKALERGDSDLILAGGVFSPGPGNSCLFSQFNGLSATGSRPFDARADGVIFGEGAGVVGLMRLKDAVAAGHRVHAVIRGAGLSSDGRSSSANVPRSEGQVAAMEACYSGAQVDPASVQYIEAHGTATPAGDATELRSIARVFGGKRSGVQLASVKALIGHVGWAAGAASVIKLCKAMEHRLFPVQSNFDAPGAALRAMGPGFEVNTREQPWPENGELPRRAATNGFGFGGTNAHLVLEEYRGPSSAPRSREGTSSEAELVVVATEGLFPDGRGRPEAGVPVEVGTRFDLKAMRLPPTVRLLPDISEDMDATQHLGLVVASALAQKLGTFDALRSGTAIVLGLEGKTRRGVEAVQRVLAFTLQRRLKEKARREPASAAVLPLAERLHSAVMGSLRPSGPYTLQGMMPNVTPGRVAGALDVKGPNFVVDAGAASSSAALQAARGLLESGFELVLVGSTHIGRPGEVGGAQQPEEGAALFAVTTAEKARRLGLKPMCHLQLSTRGTKGTGAGVDLPPHSAAESLALLRAVQAAADGRAGTLRFHPDAATGVRLEVRLHPMADVQDVEGSLPSLRARSEAATGGSFEAQPRPMSDGQPVESMQSSSRAHANAATEGRLGVSSRAAEQGGRIDASTSPLRTHPDAVTDGRSELPSRPSEGMRLAPSRPVESASSPVDGASGAESQAASGGFDHAAPIQYLSPVLVERPARKTQPSYLRGRRVLFIAEDVALARELAARAEALCGTEHVILCPGTGSDSGRLRYVDLTTDTSAEAGLAALGFEPEVILAVSRIEAGALEAAVVADTAMKHGALELLFLAARRAYERLSRGEVALVSLCIGAVGPRRCLHPMSGLFAGMLKSIGREVPARNVRAVSTTAMPIQKALELAEAELGSDVDGNHSIEVCFEGPVRCVRVLRVTDVTADQAATLDSRSVVLLTGGGRGVTAVLAGALLKRFGCKVVLVGRSDPDEAPLRVLQAREEDLPAMEREFYASELASNRGVRMPELRKRFERFLAARELKATLEGLGRLPGEVLYRAVDVTRAADVDRVVQEIVDTHGRLDLVVHGAGTQTSKKLNRRQLGELRTNLGTKLMGLRNLREACVSRLARPVPFHVLTSAFSYIGNDGQADYGAANEALDRLCAWVSDASQEVRWCSVGWLAWDGIGMTRGSEYRVLGASRHLRGIRAEEGEALFLQLVDGRPRQAINVQLTESERSYYALEVLPAEEARSLSAGPVQRELVVDAASVPCLEDHLVRGTPTLPGAWALDLMLQAAVGNGRPELRTVTIEGVRFSRFIRVKPGSRQHLRAECTPLVDEPGRHGVRVRLMGDIVHASGVVLEKDLVYAEARFTLTAEPPRGTPELDAAAPSGQALRVHDPHCAAGAPIELRKMFDCLEEIHIEPSARFARLGLPTEPRQAGSTVPALVLDAALRLSAMHVDGESSAVFAPIQFQRATFDRGLVDVRGGAPLHLSLKALPPRVDGDLLECGTVAALDEAGRLRMLLEGGLARPMA
>NZ_CP017172.1|WP_140798399.1|4119998_4121504_+|SDR-family-oxidoreductase
MTTHASHQGTYAVEHVLQRIRRCAADVTRYPMDILTADAQLEDELGIDSVKLAEIAAVVGREFNTPPERLPRGAQARTLGAMAEVVARLLADAQPAAVATPPPAPVAAPVSPVASAGPPVENLEARVRAVFARVTRYPEELLTPEADLEDELGIDSVKQAEVMAVLIKELGLTDAPQPSQRLRTISSICEMARARLAVAAPVREDRAPRQSPPSAVLPFAGKVAFVTGSGKGIGKVIAARLASSGATVVVNSFHSRDEGERTVQEIVDAGGKAFHAWGSVAQEEHLDRMFASIEAQFGGLDFLVCNASNGLIGPFDRITPRDWDKAFRTCITGTYECAMRARPLMARRGGGSIVTMSTSMSQRYMHDLGCQGVVKAGVESLTRYLAAELAPDGIRTNCVSAGPVHGELLRMFPDAASRVARWESATPGGEICTAEDVADVTELLLGPKTRRVNGAIWVVDAGLSGTVDGLLPGAPEARRPEGQRWSHSSEHDVRALLALDS
>NZ_CP017172.1|WP_174259287.1|4118748_4119864_+|Gfo/Idh/MocA-family-oxidoreductase
MAQGSSRRIRYAVVGAGNIAQVAVLPAFQHARENSELVALFSSDAEKRDVLGKKYGVRHTASYDDLEQVLRDADVDAVYIALPNTQHRAFTERAARAGVHVLCEKPMATSVEDCEAMIRVTDENHVKLMIAYRLHFEEANLRAIDLLRSGRLGAPLMMSALLTQQVRTGDIRTRVDVGGGALLDEGPYPINAARYLFRDEPTEVFCYTNGEQDPRFKGVDATAFALMRFSNGRIAQFGISHAASAVSSYRVVGEKGDLLVESAFGYEKERKHVLTLEGKTEERVFATHDQFAPELIYFSKCVLEDQEPGPSGREGLADVRVITAMQESARTGRPVKLDAFPMKRRPSLDQLIVRPAARPPEPVNAPAPAQG
>NZ_CP017172.1|WP_162521043.1|4136153_4136327_-|hypothetical-protein
MPLSAPDSGDRPKGLVARTPEKGASVAPSPDRLAGAGTGGTEPKTRFDPTGASEADG
>NZ_CP017172.1|WP_140878360.1|4136496_4137420_+|hypothetical-protein
MDGARTSENGSSQRIRPRVVLAILVGLIVVASLGYVALRNRGVEIPANVVDSTDRASVLLRRDDATSRKQAIERLRSIAIENPGYVDVQAELAVALTLNLSDVQADAERLRLRGDAIARGLEAAAKMRVLADQVARRTSLQQEQEATARDMASLRVTTATLRKELDVQLAQLNKAPESEPPSAAAARLKARALHASVLAAPDSLALAERLRNVESAPYPWSTLARAEYALVAGSPPESLQAVAKDLEALRQADSTLLRAYLLGARVALKLKDTAAARSLLDDAVALNPNHQAAARLIAQIDADAASP
>NZ_CP017172.1|WP_140791437.1|4137586_4138768_+|glycosyltransferase
MAEVFFWCAVLLLAHTYFLYPLSLFLLEGAAQVLKNARDVRRAETVNHGSGGQRALPSVSLVVAAYNEVSCIQQKLENSLALAYPAERFEVLIGSDGSSDGTDDIVRGCSDARVRLSPAPRAGKTTVLNRCIPMAQGDIVVLSDANTMIEPEAIERLVRHFEDPEVGAVCGKLRLYNPTKQDYEESAYWSYESLIKMYEGRRGAVVGANGGLYAIRRSLFTQLPPSTIVDDFVIPLRILDQGYKVVYEEHAVAHEETTEDYGKEFGRRARIAAGNFQSIRMVPGLLLPTAGFPAFAFWSHKLLRWFAPALMALALVANLFLLDRLFYQFTLFSQVLFYALAYLGKTGVLKRGTAKKAASVAYYFVTMNLAIVVGFWRFLRNSQRAAWDRTARA
>NZ_CP017172.1|WP_140875057.1|4138786_4139635_-|CHAP-domain-containing-protein
MRTVTLMGILATLATGCATTGAPLEPWLDSYSLRYRSASPPAFPRESLSKQVATAAPKAPAERPGTVAARPAKAPGGKSRAMPARATRPTPVAGDARAKVVTTARSLVGKTQVALNGRKYPSDCTGLIEGVYAQAGVTFRGTVQPGDNGVTAMYRFARSRGRVYAEERPTPGDLVFFNETYDQNRDGRRNDGLTHVGIVENVSASGTVTVIHRVRRGVVRYRMNLERPHLRRDPKTGEVLNDMLRHPGPNREPVLTGQLFGGYGSVLPKSPKAQKPVPVALR
>NZ_CP017172.1|WP_140875059.1|4139686_4141462_+|HEAT-repeat-domain-containing-protein
MSSKNLPRQPSVHARVSGWARVRYCSRDMASFRRALAVLLLAAGCIPSPYDRAAQKDTIDGYRAFLREYPTHADTDAAEARLEELEFEEAKRLHTVIAYKRFLEAYPDAAQARTAKTLLEGLRFNGAKETDTVAGWRQFLQEHPEGVQRDEAKRLLSEAEARELATTEDPRKLAEYLRASPDDPRRQDVEARLDAQAFAQAKASGATKLFAYLKEHPAGAHREEARVLLLLLEVEGLLVSGLVDEAEARVKAHPLGPKLTAFPERLASARAERAALARPEPLAQAAHVGHYLRGVEDLSRALVAPDALDRWQAAEELGQHVTVRVLDPLLESLRAARNPLIRQHALESLRTVLAALPKPVAEYEVSSRLDALRERATSAEMYLTVAVLLDLSGQLAQASTEYQRAAESGVPDPVILRRWVQIREERRQHFSAAVAARQLALWSLEVAQEEPVTPEGRVPLASARQLCAAAVNANFAVAAIARARSESTEFPEDLAEFERKAADAKRLADARLADAELLLREQSPGVKTCADRGVRDRLENAVKERTAALDSVATKLPQVGRLLLEVARQRDPSPQVRAAASARLTALKPVP
>NZ_CP017172.1|WP_140875061.1|4141506_4143585_+|UvrD-helicase-domain-containing-protein
MSSRTDTLQAPATTPSLRIDYAALLNEEQLRAVEAGEGPVLVIAGAGSGKTRTLTFRVARMLERGVPPEGILLLTFTNKAAREMTRRVEELAGAFVDVRRILGGTFHHAAHVLLRQYAGVLGFSTNFTVLDREDARDLMVTCIAERRLKSDKRFPRPDLVLDLVSLAANLQQPVSHVLMDRRPQMLPLAPEVLAAAARFQQRKAQMHLMDFDDLLVHLKRLLTHHPDVKAQLTERFRCVLVDEYQDTNRLQGDLVDLLAGERKDLTVVGDDCQSIYSFRGADFTNIIGFPERYPGCSVHALTRNYRSTPEILRLANTSIALNTNQFPKVLTAARSPGVKPLIVPARDAGEQAADVAQRIGELRDQGLSLEAMAVLYRAHNHSLELQLELTRRGIPFRVRSGVRFFEQSHIKDVLAHLRLVNNPGDELAFKRVIRRVPGVGPATAEHLWTALRALPEGTPLAEGLAHADVRAHLPRKAQKRFQAFGDLMGRLTLPEASPSPGRLIEDVLAGGYADFLRAEFSEEEHREDDVRQLAEFAGRFEDVARFLSEIALVSEFAAGEALREEGPEACLTLSTVHQAKGLEWRAVFVLWLADGRFPLSLATRLPEEEEEERRLFYVALTRARDTLVLVYPQSVLPRDGERILLRPSRFLQELPGGEDAPFDRCILSTLEAEPEAAVGQDGPPPGGSDPVD
>NZ_CP017172.1|WP_140791445.1|4143675_4145298_+|Hsp70-family-protein
MADRPRIIGIDLGTTNTLVASVRNRIPKIVPTDRGNLTLPSVVALSARGDLLVGGVAKDQMVTNPKNTLWGTKRLIGRKYNSKSVEELKGYFPYDIVEGANGDTAVMMGGKLYSLPQVSSFVLGQVKTIAEQFLGGPIEGAVISVPAYYNDNQRNAVKEAGRLAGFDVKRIVNEPTAAALAYGFNRGLDQKVLVYDLGGGTFDVSVLHLAGNVFEVLATGGDTFLGGADFDNRIMEYVLERFREETKVDLNTENPIAIQRIKNAAEAAKIDLTLIPNVVIDLPFIDERKGKPVDLRIPLTREFLNSLTGDLVDRTFEICDRVLEEKGISRAEIDEIILVGGQSRMPLVQQKIQAHFGKAPRKGVHPDECVALGAALLGDSLGSIDAVTLLDALSMPIGYAMPNGRVKRIIEKNSLIPMVKSFRLPPPKEPGSPFIELDIYQGDSDLLVDNEYLGTVRVPSAAAGRKIDFRLTEECLLQVTVEEASGMRKVDLATRDTPEQLKRALQEVASRHSQQVPSSSSSGSDDRGLFSSIKSIFRRG
>NZ_CP017172.1|WP_140791447.1|4145306_4145732_+|hypothetical-protein
MAKFPSKEWVDEAVRLTNEDPECAMAGKGWKGDFGAVVEAEPGMLARAFVVHVVPGDCRIEKARVLADPDDLDELEPVYLARAPYSVWKQLLKGTLDPVEAVLKRRISMKGDLQPLIERMKYKGIADRVFAQLQTQFIDEP
>NZ_CP017172.1|WP_140791449.1|4145744_4146014_+|hypothetical-protein
MGITDDLKKQALNVSGKAMEKLMADDRRAMAIANAIGKAQRGKQALDRGQEELMKALNFAPRSEFKALGKQLSGLKRRLRELDEKLGAL
>NZ_CP017172.1|WP_140875063.1|4146323_4147283_-|TerC/Alx-family-metal-homeostasis-membrane-protein
METFPSVGSPGLWAGFVAFVIAMLALDLGVFHRKAHVVKFKEALGWSALWVSLALVFGAGVWWKFGPEPGLQFITGYLIEKSLSVDNIFVFVVIFSALRIPSLYQHRVLFWGILSALALRAIMIFAGVAMLARFHWLIYVFGGFLILTGVKLFLQRNKEDNPEEGALMRLARRTIPSTPNFDGHHFFTVENGRKLATPLLMALLLVEASDILFALDSIPAIFAVTTDPFIVFTSNIFAILGLRSMFFMLAGAVEKFSYLKVGLSAVLVFVGTKMALIDFVKVPPEVSLSVIAGLLGASIVASLIKSRNTPTGDADAPKV

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_9

5207704-5207879

Orphan

Consensus_repeat	Method
GCCTCGCTCGCGGTACCACCGGCACC	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP017172_9

>merge|NZ_CP017172|9|5207704-5207879|CRISPRCasFinder
GCCTCACCCGCGGTACCACCGGCACCCGAAGCACCGGCCTCGCCAGCCCCCGTAGCCGAAGCACCGGCCTCGCTCGCGGTACCACCGGCACCTGCGTTGGAGGCACCCGCCTCCCCTGTGGCACCACCAGCACCCGCAGCCGCGACTCCCGCCTCGCCCGCGGTACCACCGGCACC

>NZ_CP017172|9|8|5207704-5207879|CRISPRCasFinder
GCCTCACCCGCGGTACCACCGGCACC	CGAAGCACCGGCCTCGCCAGCCCCCGTAGCCGAAGCACCG
GCCTCGCTCGCGGTACCACCGGCACC	TGCGTTGGAGGCACCC
GCCTCCCCTGTGGCACCACCAGCACC	CGCAGCCGCGACTCCC
GCCTCGCCCGCGGTACCACCGGCACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140792544.1\|5213993_5214629_-\|uridine-kinase	unknown	unknown	gnl\|CDD\|235492
NZ_CP017172.1\|WP_140875772.1\|5205511_5206147_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140875768.1\|5200824_5202510_+\|response-regulator	unknown	unknown	gnl\|CDD\|224117
NZ_CP017172.1\|WP_140792552.1\|5218644_5219337_+\|response-regulator	unknown	unknown	gnl\|CDD\|223816
NZ_CP017172.1\|WP_174259314.1\|5211995_5212910_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140875770.1\|5204475_5205480_-\|biotin--[acetyl-CoA-carboxylase]-ligase	unknown	unknown	gnl\|CDD\|223417
NZ_CP017172.1\|WP_140875781.1\|5217471_5218347_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259313.1\|5209783_5211982_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP017172.1\|WP_140798697.1\|5197708_5198833_+\|alanine-dehydrogenase	unknown	unknown	gnl\|CDD\|240630
NZ_CP017172.1\|WP_140875777.1\|5214698_5216387_-\|DUF692-family-protein	unknown	unknown	gnl\|CDD\|377459
NZ_CP017172.1\|WP_140792536.1\|5206124_5207042_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|379311
NZ_CP017172.1\|WP_140798704.1\|5212961_5213993_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|224932
NZ_CP017172.1\|WP_140875783.1\|5219305_5220946_+\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_140792529.1\|5202561_5203695_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140875751.1\|5199739_5200648_+\|zf-HC2-domain-containing-protein	unknown	unknown	gnl\|CDD\|227949
NZ_CP017172.1\|WP_140878409.1\|5203691_5204462_-\|type-III-pantothenate-kinase	unknown	unknown	gnl\|CDD\|237349
NZ_CP017172.1\|WP_140875779.1\|5216467_5217283_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379326
NZ_CP017172.1\|WP_140792521.1\|5196218_5197523_-\|radical-SAM-protein	unknown	unknown	gnl\|CDD\|100105
NZ_CP017172.1\|WP_140875785.1\|5220933_5222112_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_011554150.1\|5199075_5199717_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|236608

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140792544.1\|5213993_5214629_-\|uridine-kinase	gnl\|CDD\|235492	PRK05480, PRK05480, uridine/cytidine kinase; Provisional.	5.51742e-108
NZ_CP017172.1\|WP_140875777.1\|5214698_5216387_-\|DUF692-family-protein	gnl\|CDD\|377459	pfam05114, DUF692, Protein of unknown function (DUF692). This family consists of several uncharacterized bacterial proteins.	1.8914e-23
NZ_CP017172.1\|WP_140875768.1\|5200824_5202510_+\|response-regulator	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	2.00952e-18
NZ_CP017172.1\|WP_140792552.1\|5218644_5219337_+\|response-regulator	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.11653e-76
NZ_CP017172.1\|WP_140875770.1\|5204475_5205480_-\|biotin--[acetyl-CoA-carboxylase]-ligase	gnl\|CDD\|223417	COG0340, BirA, Biotin-(acetyl-CoA carboxylase) ligase [Coenzyme metabolism].	1.52628e-86
NZ_CP017172.1\|WP_174259313.1\|5209783_5211982_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	7.21863e-14
NZ_CP017172.1\|WP_140798697.1\|5197708_5198833_+\|alanine-dehydrogenase	gnl\|CDD\|240630	cd05305, L-AlaDH, Alanine dehydrogenase NAD-binding and catalytic domains. Alanine dehydrogenase (L-AlaDH) catalyzes the NAD-dependent conversion of pyruvate to L-alanine via reductive amination. Like formate dehydrogenase and related enzymes, L-AlaDH is comprised of 2 domains connected by a long alpha helical stretch, each resembling a Rossmann fold NAD-binding domain. The NAD-binding domain is inserted within the linear sequence of the more divergent catalytic domain. Ligand binding and active site residues are found in the cleft between the subdomains. L-AlaDH is typically hexameric and is critical in carbon and nitrogen metabolism in micro-organisms.	0
NZ_CP017172.1\|WP_140875783.1\|5219305_5220946_+\|GAF-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	5.67157e-42
NZ_CP017172.1\|WP_140792536.1\|5206124_5207042_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|379311	pfam13646, HEAT_2, HEAT repeats. This family includes multiple HEAT repeats.	9.34712e-09
NZ_CP017172.1\|WP_140798704.1\|5212961_5213993_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|224932	COG2021, MET2, Homoserine acetyltransferase [Amino acid transport and metabolism].	1.64492e-47
NZ_CP017172.1\|WP_140875751.1\|5199739_5200648_+\|zf-HC2-domain-containing-protein	gnl\|CDD\|227949	COG5662, COG5662, Predicted transmembrane transcriptional regulator (anti-sigma factor) [Transcription].	5.86716e-14
NZ_CP017172.1\|WP_140878409.1\|5203691_5204462_-\|type-III-pantothenate-kinase	gnl\|CDD\|237349	PRK13321, PRK13321, type III pantothenate kinase.	1.70655e-164
NZ_CP017172.1\|WP_140875779.1\|5216467_5217283_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.85499e-09
NZ_CP017172.1\|WP_140792521.1\|5196218_5197523_-\|radical-SAM-protein	gnl\|CDD\|100105	cd01335, Radical_SAM, Radical SAM superfamily. Enzymes of this family generate radicals by combining a 4Fe-4S cluster and S-adenosylmethionine (SAM) in close proximity. They are characterized by a conserved CxxxCxxC motif, which coordinates the conserved iron-sulfur cluster. Mechanistically, they share the transfer of a single electron from the iron-sulfur cluster to SAM, which leads to its reductive cleavage to methionine and a 5'-deoxyadenosyl radical, which, in turn, abstracts a hydrogen from the appropriately positioned carbon atom. Depending on the enzyme, SAM is consumed during this process or it is restored and reused. Radical SAM enzymes catalyze steps in metabolism, DNA repair, the biosynthesis of vitamins and coenzymes, and the biosynthesis of many antibiotics. Examples are biotin synthase (BioB), lipoyl synthase (LipA), pyruvate formate-lyase (PFL), coproporphyrinogen oxidase (HemN), lysine 2,3-aminomutase (LAM), anaerobic ribonucleotide reductase (ARR), and MoaA, an enzyme of the biosynthesis of molybdopterin.	1.93876e-13
NZ_CP017172.1\|WP_011554150.1\|5199075_5199717_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|236608	PRK09652, PRK09652, RNA polymerase sigma factor RpoE; Provisional.	2.52347e-58

>NZ_CP017172.1|WP_140792536.1|5206124_5207042_-|HEAT-repeat-domain-containing-protein
MKPVLLLASCVVLLLGACRWQSPRYPVAPVELSGATLRDNALLGLAPEGVATLFTAALKDSGRFEQKGAEAPREERPWRLTLDVPFTREVLKDGDPRSFAEVGANLVLERFGGSLPQRYELVGLGEAPVEEDSPAGRQKAMRTALANVLRQVTESAVMQLTALDRTDEELVLDLKASDSRVREFSLRTLAERQHPAAAPLLIDRLKEATDAETVRRTMGSLVEMKARAAVPVLIDLVRGRDLGFVQEIVFAVGEIGGPEAEAYLYTMAQGHDAPAVQAAAQQALDTLYASRKHSPAEARGPSRAD
>NZ_CP017172.1|WP_140875772.1|5205511_5206147_-|hypothetical-protein
MAPAARTDIDMKRSFGMGGAAVLAALVLGTGCSKNVDAAAGASASTDDVSAYYPLAVGNSWTYRINGRDDKQVTVEILKEEAGVFHDSQGGQLSLDGYGLRDPKRYLLRGPVRTGHSWTNVVSVSSTERYHIVQAGDSCETPAGTFPNCVQVEGRNRVDAKATLVNTMTFAPGVGVVRIEVAVETNGQLMPQTSLELTAWQLRDGAAPPSG
>NZ_CP017172.1|WP_140875770.1|5204475_5205480_-|biotin--[acetyl-CoA-carboxylase]-ligase
MAANANEQTQEELILSFLSESGGDYTSGEVLSSKLGLSRTAVWKHVEALRAKGYRIEAVSARGYRLVAVPDRLTSLEVGPLLGTHDLGRTIHHHESLPSTNEKAFRLAQDGAEHGEVVVAEQQTAGKGRRGRTWVSPPGLNLYFSAILRPDLPPQRAPELTLVAAVALAESLRDAGVEAAIKWPNDVQIDGLKVAGILTELSAEPERVHFVIVGVGVNLNSQAEHFPEELRATATSLSLALGQPVHRTRFAASLWTRLEEWLDLYLATGFDAVRARWKALSSTLGQDVLVRTDRQELRGRAEDIDPSGALLVRTAEGSLERVLAGDVEQLRPRR
>NZ_CP017172.1|WP_140878409.1|5203691_5204462_-|type-III-pantothenate-kinase
MLLAIDVGNTNTVLGVFEGRRLLDHWRVETSTRRTSDEYGILVRQLFAHSGIDPTKVTAVAVSSVVPPLQSNLEKMSERYFRIRPMFVGPGVKTGMPILYDNPREVGADRIVNAVSAYEKHHAGVVVVDFGTATTFDAVSPKGEYLGGCICPGINISMEALFQNASKLPRVEFARPPHVIGRNTVHSMQAGLVYGYVGMVDGICTRMQAELGFPVKVVATGGLASLVASESKVIHQVDEFLTLEGLRIIYGRNHAS
>NZ_CP017172.1|WP_140792529.1|5202561_5203695_-|hypothetical-protein
MTTAAPNAVPTPPPGCPFDAEFLPPNLRKHVDPAAPVPLRMMAAKSLVPLSPSDMVGALYMLTYDPDANVRETAAKTAAGLPDRILGSALRDEEVQPQVLGYLLGLVKGNEAYAEMLVLNASTPDDAVADVAKDCSPKLAEIIGQNQLRLLRHEDILRNLCVNASAPVSLIDNVCDFAVRSGLTLMDVPQMKAARVRVFGPEAAEAPPPQGPTAEEVLQEFQEAADESAAPMEEGKRLTLAQRIMRMSIAEKIKLATLGNKEARTALIRETNKLVAVAVIRSPRITDGEVLSFATNRAMMDDVLRVIYSNREWTKNHKVKMALVKNPKVPLTVTMKFLNSFRDAELKDLSRDKNVPAAVQGFAKKLHEKKTTPKKQG
>NZ_CP017172.1|WP_140875768.1|5200824_5202510_+|response-regulator
MSKKILIVESDTALSATLRSALEGRGFTVEETTDGKGSVEQIRRDRPDLVVLAVDLSAGQNGYLICGKLKKDDDLKNVPILIIGNPDGFAQHRKLKAHADEYVAKPVDADQLVERAGALIGFPELPATEDVVDESLTLDALGDEPMTADFGEEISVETAEEPPVTGEELDLDAAFGDLSAPEEPPSFEEEVVVAPPEAVVEGVEEDFSTLDSLGTDSDDPLEGLDDSDEKTVIGFIAPAPVAAPPPEPPRAVAPPPVPRPIAAPRPAPPPVAVAPAADAAELRSLRTRVAELQAELDDSRGMASHAEERVRDLEAQLESQATELEAARASSGKNDKDTFALRDAANKKDKEILRLKTELNQKDQEIIELKDQSLELEQKASTAESELAQRDAQLKTLSARADSLASDRKRVDQQLAAAKEEARGASAQLTALQTELDQHQAQAQAYAAELEELRARAGQLEADVQAAQHEAEDLRVQLGQAQVELSEQSSRASAEADELRGRIAELEVATARNEERVTRLYARIKSEEKLREKTKKALVIAQQLLDEPASSVADDASEAAA
>NZ_CP017172.1|WP_140875751.1|5199739_5200648_+|zf-HC2-domain-containing-protein
MNCQDLERLLYPYLDGEFQPEERVDLETHLSGCADCRRRAEEEKQMQQALRRAARHSVSGMRAPASLRAGIQVGLKQEQRRVQFGVWLRAGAMALVVVTVGGGWAAFHAEQRLSAARTEAVQRHSKSKALPFEIASNAPEQVEEWFKDKVDPRITVPQIPKAKPLGGRISILNGREVAYISYETLPDNEGEPSRRLGVFVLPGNDEVSIPKFQALQAVEVDSAQGFNVVTWRDDEIVYEMVTDMDESDIRRMLAERDSGEKLARKSAPEADEPLYSLPPAPRTPRSRPPISVEPVTYPTYPQ
>NZ_CP017172.1|WP_011554150.1|5199075_5199717_+|sigma-70-family-RNA-polymerase-sigma-factor
MLDFRQPNRTKQEFEELALAHLDPLYSAALRLTKNERDAEDLVQDTCMRAYRFFDKFERGTNIKAWLFKILTNTFINRYRRKVKERTVVEGVEREAVHERFVSRDATDFAANPEQYFFDRLLSDDVLRAIDALPIDFRLVVILADLQEFSYKEIAEILECPVGTVMSRLFRGRKLLQKNLREYAEGQGVFRHDGEPVNAPADLEEYRHRKKTG
>NZ_CP017172.1|WP_140798697.1|5197708_5198833_+|alanine-dehydrogenase
MIVGVPKEIKTREYRVGMVPAGAAAFIAAGHTVLIETNAGVGSGIPDSEYQRVGAQIVSTADEVWKRSEMIIKVKEPIAPEYARIQPGQVIYTYFHLAGVDPELTKTLLQKKAAAVAYETLQPDDGSLPLLKPMSEVAGKMAIQVGAKCLERAHGGKGILLGGVPGVRRGRVTVIGGGVVGLCAAKVAVGMGAEVTIIDVNMERLTYLDDVFLGRVGVLASDSESIARSVREADLVVGAVLIPGRKAPKLVSEALISEMSPGSVVVDVAVDQGGCIETCKPTTHDNPTFEVHGVVHYCVANMPGAVPQTSTYALTNVTRPYSLMIANQGLAAAVKADRALSRALNTYNGHVTYEAVAKDMGYPYMPIADALAGK
>NZ_CP017172.1|WP_140792521.1|5196218_5197523_-|radical-SAM-protein
MTSAPKLLFADPKGRVMEHPYLLATLRSGEELVPPQDKPIPLPSAGRLVHLPGRLPVGLHPETGELELVREMKVGGKTFVPNAVGALLPPGYTRTFLPGEVKGSGPVLPQWAYTAAAWVGEGPVAWAIHTDRRSHWDPERFSTPDMKDLVAKHMARFPDNRVLKQLKTCAMLYRCFTSQNTFYVRDEAAIPASVMCNARCVGCISDQPADGPPASHERMDDGPTGEEMGQIGLFHLEHAPGRTMVSFGQGCEGEPLTRWKQIAEAIRYMRARTQAGSININTNASLTRGLEALFDAGLDAIRVSLNSAVKDLYEAYYKPVKYGWEDVEASIALARERGAYLALNLLLFPGVTDREGEVRALERLVKKYRVDQVQTRSLCIDPLQYLEVARERGAGGEPVGIRTLLQRLKAARPGLIVGNFARGLEERENAAGLR
>NZ_CP017172.1|WP_174259313.1|5209783_5211982_+|PQQ-binding-like-beta-propeller-repeat-protein
MTRIRIGQRWKREPAASPLDSIALELDGVDLLSGAVEESLAEVVPSLVRSVAALAGGRQKLAQVSLPEAHLELVLRRMGPEVELLVANLSRPARLMRPPVRVELEELVEAVREAGERFLADVTRAGPKSLATTVGQALKEPLKGLNRPARPPDEAPARPATRRVEPTEVPGFGFELRDAGVPMGRGAARGTAGLLAPLLASGEVWLSLPGKPEAWRVPGPPFLTALELSRQAVELARAVELGESRFELAPAGAKPSLLVDLKSGQAKAGRTGTPFPLAGNVLAAALFHLGESLAAAFAEADRALVANPYRMELAERCREGLSHLRGPVQPPEARGAAREKKTRATGQGTSRPLKVPGRLRRLRFAKLWEKRGLPDAEESRLLLGRHGPVYCAPQLASAFSRKDGALLWKRAAALGVAASADGHAVAADIARVYGFTGRGGGARWLHDHDGIPLGPLLLRKDGLLLTLSEDRTVVAFAEATGREVWRLAPPRTQRSWLATQGHRALVGTDSGYLYGLDLEDGQVRYRMRAPMPFHGPPVAWGRRFLAMLGRGSHWAVLLADAHTGESVWTHEPDLSHLSAPLPVGSRVFIAGEREREGMLLCLDAKGRRLWERPLNLGPGPYALAPLPRAVVVTSASGAATRVAASGTVDWRVGAAGEPLISALPAHTARDVTLVPGERVRAVDPRGGQVLAEVQAGVGLVALQADVRLNLYFLDDAGTLSAYRLGSHFTVVE
>NZ_CP017172.1|WP_174259314.1|5211995_5212910_-|hypothetical-protein
MKRYFGVIVIVAGVLLAAVMSYRSASGRALEAQRDADQQRIHAEYLERVGWMRANPDEASYRDELKPFFKHYFEQVDAHLTRFKGNTKFDDYLLELEKREESGAKDDRANDRKAFYEYTRKTFDSLREGRYRPVWTATDKGMRLDIISSDVVMVLGKPQIRLQLAVWGAQRVLKDDGKVLKMMTSATFDTVWKLTDAKGKLLGEMRGADPSMKIDHPERFVRAFPPQMVLGHYDLDLLPNEVAKVEMTINLSSSAASGGTAASTYVWKLDVPSEWKLGAGESWEGATQEERPEEEIDPSKAAAN
>NZ_CP017172.1|WP_140798704.1|5212961_5213993_+|alpha/beta-fold-hydrolase
MIQATGTHLFTTPLPLEEGELLGNPQVAWAAYGEPSDGKAVVLLHDLAHSHLALGPPEDSAYQPSGWGRALVGTNLALDPAITPVFSPGLLGSPFGSTSPATVNPASGERWGLELPPLTVQDMARAVSATLRARGLTQVRALVGVGLGAHVALRLASLFPDLAEGVVAIGAARALPEGVREKLGLSWQVLRADPDYRDGLYALDAPPRKTMRKLRLDFQKLLCGREFLASAYPAPEAARAALETEADAFADAFDAVSWASLCSAYAGSDVSDGFSRIRARVLLVTGTSDAMAPVNRVRDTYHLLSAAGVSARFLELPGPGDHAALLQDAERLHGPLSDFLRRC
>NZ_CP017172.1|WP_140792544.1|5213993_5214629_-|uridine-kinase
MASPLVVGIAGGTASGKTTVARKVREALADCRVAFIDQDSYYRDLKDLPLADRREVNFDHPDAFDRELLVQHLQALKSGQPIQKPVYDFVTSSRTPQTKNVDPGDIILIEGILVLHMKEVRDVMDVKIYVDADDDLRILRRLTRDIKDRGRDFDHVVSQYLRHVRPMHMGFVEPSKHFADIIIPHGGNNEIAIGMLVGALRGKLSGAVKRD
>NZ_CP017172.1|WP_140875777.1|5214698_5216387_-|DUF692-family-protein
MAVDAGRVYVERMTHAVSETWTLPWRGLGLSSNLSVADVPQPYRLLDESPGLFDYVEYSAPLSLEESKAHASLFPEMWRRRQDVPVLFHPVHLNLWGPALEPGQALRDLDAHARAVESPWVGNDVGWWHVDGQPFPGYLYFTPPFNEAGLEACVSHALHVQRHLSVPLVLENPAVLARRGQWHVLDFMAKLHARTGAPLLLDLGHLLSHQLSAGLPLETGLDGFPLDQVIELHIAGGVVTHRGPRSFYVDDHTQPVREELFDLLASLIPRCPSLRAVTFEGDGHPPEVARMSLRRLRQLVPSGARPPLTWRVPAAVAAVPPLTEDSHPWALFDAGYAAAPAASVEDEAGTLADQDFRLAVVAEVLDRDWPLTRLLLAGTREGLAAFTGSKEYRKLFDSVARTPGQSFASWAMRRLRESPDEGASAALTLEMLLPSLFTRRVPAPAPGQVGLMEDVRVGSLPVDLSELVHSARAVCRHLTARAWACGTLELSGLDSLNQVARRPGPGPWSFVARRKAGGPEVMSVPPALGEFLGMLAVRPMAEAEVSPGLLEAARGRGLIRRG
>NZ_CP017172.1|WP_140875779.1|5216467_5217283_+|GNAT-family-N-acetyltransferase
MPTPSRVEIDESNAHYRGAWRLFALGSKSGEVVERPEVYITACHVAWSMMNSAFLRAPVETEQALAAAAASAARYFSAGKHGWSFVICDDWLAPSVRDNAPSILAWYGLKSEMGVTGMVADRLAPAIHPQPPFAVRPVTDTWGRQAVADINANAYDVPRHFGREAFDEDTLYTPDCQGFVACRDEEAAASTVVLRVDAAAYVALVATQPQHRRQGAAEAVMRHALAKAHQDWGTERTVLHATSAGEPVYTRMGYRPVTRFRMYMAPPPGQG
>NZ_CP017172.1|WP_140875781.1|5217471_5218347_+|hypothetical-protein
MPHVLHRPATRSPYMAKWDDLVLAIPPHAGGRYQAPAAVTLLETLLGLHEAQLTLLRGLHRDVRPLREGPFHAGRLHLEAVRAPQATRDEQLERLKSARSCFTDAMGTERDKARLSFIALHLGLCWLMLGAERDAREWTQLAHRTAVEAMKDILVEASKHQGLTQNRYLDPALTFFMFFTSTATLGAGYLFWDRVLSKRTGTVMRRALGQMQALADYVDMLGEVRLRLGELPHDVARYELTHGVDEQQSVARITIRKLISDREAIYFNGRETRKVTWNDQERSEVITRELI
>NZ_CP017172.1|WP_140792552.1|5218644_5219337_+|response-regulator
MAERPTVLVVDDDPHLREIVRFALEQGGFRVDEAADGRAALTQVDRALPALIVLDIMMPELDGLAVCREVRRKHELPIVFLSSRDDEVDRILGLELGGDDYLTKPFSPRELVARVKAVLRRARPAPEVEVPAARMQSRGPLRMDAERWRAWWQDTEVVLTVTEFQLLATLLRVPGKVFTRDELMNRVYDDVVVSDRTIDSHVRRVRQKFASAGGDVIETVHGLGYRLALP
>NZ_CP017172.1|WP_140875783.1|5219305_5220946_+|GAF-domain-containing-protein
MALAIGSPSPERRARPRLWLVFAAVGVAGFALTLAGLAFVRVYDNQLIRQTESELIAQGAVVAEVFRERLRATVPEGVYGRERTAPWPFPIPDDTRLRPILPSLRASDASLPPGDTPRPSLVPAEPLSQAAGLQLTPLLEQVRAATLAGIRVVDTEGVVVASSSPALLWTTLADRTEVQRALRGEPVSVMRRRVADPEDTPLASLSRDTGIRVTVALPVLEGDRVWGAVVLTRTPMTFAKATYADRWNLTATGFVLLGAVALMSLAAAALVGRPVRALVKQTRAIAMSDPSGFEPMARPVVAELAELSESLAGMATALRDRNQYIRSFAANVSHEFKTPLASIQGAVELLRDSADAMSPEQHARFLANVDADARRLTRLVQRLLELARADSMTATLAQVELGPLLEGLALRARAEGATDIHVTAPPAGLKVSLPQEVLDDVLWQLVTNARQHGGDTIRVDLSVEQAPEADMVRVVVKDNGKGISEANRARIFDAFFTTARERGGTGLGLTIAQSMLRAFHARLELLPSDTGTTFAVVAPVPRLQRK
>NZ_CP017172.1|WP_140875785.1|5220933_5222112_-|hypothetical-protein
MWTVPLFVGLLLTTADGSASTSPSGTATVPLQELIPLYAQRQSAPVEAPPMAALVKSQLKGRLTADALFVDGHFDVEVLADGRWTQVRLLQLDADTFPAALPALEEGSVGVVDGYLCLLTRKAGRYVFDVGVSIRSPGAGPERRAQLRFGPHASPVPLALEADTSVFTLTEPVASMGGESHAVYPVQGALRVGWRAAVARVAQSQKQQVRPPLEPRITEATASWVSTLEGRATLRVSYALSLDREQPLELVLPEGHRLERVTLNAIPVPVESENGTLALKATPARLGETGGTLEVVLSRELGVFHLSGRLKLALPRVSWPVAELRARAHFPAVFNYRREGGSLEQYESTGAVAAEASGLPGKALHFRQFLVAASSPTLELGYSVDISDSYFR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_10

5282006-5282148

Orphan

Consensus_repeat	Method
GGATGTGGAAGGAACGTTCCGTCCAG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP017172_10

>merge|NZ_CP017172|10|5282006-5282148|CRISPRCasFinder
GGACGCGGAAGAAACGCGCCCTCCGGGCAACTCCGCTGATTCCCCCCCCGGCGGCGTGGATGTGGAAGGAACGTTCCGTCCAGACCTTTCCGCAGAAACGGCCGCTGGAGCGAGGGCGGACGTGGAAGGAACGTTCCGTCCAG

>NZ_CP017172|10|9|5282006-5282148|CRISPRCasFinder
GGACGCGGAAGAAACGCGCCCTCCGG	GCAACTCCGCTGATTCCCCCCCCGGCGGCGT
GGATGTGGAAGGAACGTTCCGTCCAG	ACCTTTCCGCAGAAACGGCCGCTGGAGCGAGGGC
GGACGTGGAAGGAACGTTCCGTCCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140792651.1\|5289320_5290100_-\|histidinol-phosphatase	unknown	unknown	gnl\|CDD\|273949
NZ_CP017172.1\|WP_140792635.1\|5278311_5278986_+\|GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|234745
NZ_CP017172.1\|WP_140798746.1\|5290096_5290858_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	unknown	unknown	gnl\|CDD\|234996
NZ_CP017172.1\|WP_140875807.1\|5279858_5280932_-\|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl\|CDD\|319743
NZ_CP017172.1\|WP_140792649.1\|5287995_5288445_-\|DofB-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140792656.1\|5291390_5292107_-\|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase	unknown	unknown	gnl\|CDD\|240083
NZ_CP017172.1\|WP_140798745.1\|5286777_5287977_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140798744.1\|5282856_5284113_-\|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl\|CDD\|237001
NZ_CP017172.1\|WP_090490647.1\|5284173_5285103_-\|lipoyl-synthase	unknown	unknown	gnl\|CDD\|235493
NZ_CP017172.1\|WP_140798739.1\|5275386_5276766_-\|protease-inhibitor-I42-family-protein	unknown	unknown	gnl\|CDD\|378179
NZ_CP017172.1\|WP_140798740.1\|5276961_5278194_+\|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl\|CDD\|238452
NZ_CP017172.1\|WP_140792623.1\|5269753_5270539_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140800730.1\|5268406_5269606_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP017172.1\|WP_140792650.1\|5288712_5289321_-\|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE	unknown	unknown	gnl\|CDD\|235067
NZ_CP017172.1\|WP_140792627.1\|5271474_5271693_-\|DUF3185-family-protein	unknown	unknown	gnl\|CDD\|378652
NZ_CP017172.1\|WP_140875811.1\|5285362_5286760_-\|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl\|CDD\|235798
NZ_CP017172.1\|WP_140798737.1\|5271745_5275279_-\|ribonuclease-R	unknown	unknown	gnl\|CDD\|273947
NZ_CP017172.1\|WP_140798736.1\|5270714_5271458_+\|DUF2807-domain-containing-protein	unknown	unknown	gnl\|CDD\|371327
NZ_CP017172.1\|WP_140792654.1\|5290857_5291394_-\|imidazoleglycerol-phosphate-dehydratase	unknown	unknown	gnl\|CDD\|153419
NZ_CP017172.1\|WP_140792637.1\|5279035_5279869_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293801

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140792651.1\|5289320_5290100_-\|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_CP017172.1\|WP_140792635.1\|5278311_5278986_+\|GTP-cyclohydrolase-II	gnl\|CDD\|234745	PRK00393, ribA, GTP cyclohydrolase II RibA.	4.10325e-106
NZ_CP017172.1\|WP_140798746.1\|5290096_5290858_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	gnl\|CDD\|234996	PRK02083, PRK02083, imidazole glycerol phosphate synthase subunit HisF; Provisional.	5.02405e-155
NZ_CP017172.1\|WP_140875807.1\|5279858_5280932_-\|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.	2.79163e-98
NZ_CP017172.1\|WP_140792656.1\|5291390_5292107_-\|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_CP017172.1\|WP_140798744.1\|5282856_5284113_-\|2-oxo-acid-dehydrogenase-subunit-E2	gnl\|CDD\|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	9.70905e-174
NZ_CP017172.1\|WP_090490647.1\|5284173_5285103_-\|lipoyl-synthase	gnl\|CDD\|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	7.07392e-176
NZ_CP017172.1\|WP_140798739.1\|5275386_5276766_-\|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.	1.47775e-12
NZ_CP017172.1\|WP_140798740.1\|5276961_5278194_+\|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.	2.5553e-163
NZ_CP017172.1\|WP_140792623.1\|5269753_5270539_+\|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_CP017172.1\|WP_140800730.1\|5268406_5269606_+\|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_CP017172.1\|WP_140792650.1\|5288712_5289321_-\|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_CP017172.1\|WP_140792627.1\|5271474_5271693_-\|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_CP017172.1\|WP_140875811.1\|5285362_5286760_-\|dihydrolipoyl-dehydrogenase	gnl\|CDD\|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP017172.1\|WP_140798737.1\|5271745_5275279_-\|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_CP017172.1\|WP_140798736.1\|5270714_5271458_+\|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).	8.19087e-32
NZ_CP017172.1\|WP_140792654.1\|5290857_5291394_-\|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_CP017172.1\|WP_140792637.1\|5279035_5279869_+\|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_CP017172.1|WP_140875807.1|5279858_5280932_-|lipoyl(octanoyl)-transferase-LipB
MNTITVYRLGRVEYEDGLALMHLFSESRRQGLSGDVLLLLEHPPILTLGRAAKRENIVASDAQLAKEGAEVFETNRGGDVTYHGPGQLVGYPIFLLPEDRRDVRRYVRDVERSVMQVLAQWGITAGPIPKWPGVWIGAEGAPDARKIAAIGVHLSRWLTTHGFALNVNTNLDHFQLIVPCGIREAGVTSMQRELGRALPMAEVEEAIASSFCTVFDSERVDAPPPMRTVSIAVVKGRGPEARVLLVRRRPERGGFWQVLTGRLEAGESPAEAAARELEEETGLRVPLVDLDYRHAFALGEALPPQLVEENGFAVHVPPDADVRLGAEHDAFEWVDVPTALERLPFRGLRETVKRATA
>NZ_CP017172.1|WP_140792637.1|5279035_5279869_+|MBL-fold-metallo-hydrolase
MPFEVRFWGVRGSIPSPGAHTKRYGGNTPCVEVRCGDELLIFDLGTGARALGHALVAKKKPVKGSIFISHYHYDHLQGLPFFGPMFLPSSDLTVYGPARHGQSVKQLLSGQMVPPYFPVTADGVFRAQLTYTDLAATQTLQLGPATVRTIELNHPGGNMGYRVECQGRSVVYATDLEHGSDMDAAFYAFAQDADVLIYDAMYTEDEYHGRTGPARTGWGHSTWQAAVHAADEAGVKKLVLFHHDPSRDDAGMDRLLRQVRKHRPDAIAARESLVIKL
>NZ_CP017172.1|WP_140792635.1|5278311_5278986_+|GTP-cyclohydrolase-II
MSDTRSPQVLPTRKPTQHLERFSEADIPTERGSLRTIVFRDKRNGREHVALVVGEVSGHEGVPVRIHSECLTSEVFGSLKCDCREQLDRSLDFITQSGQGVVLYLRQEGRGIGLGNKIKAYALQSKGLDTYEANRQLGFADDLRTYDIAAEMLRSLDVRSVDLMTNNPLKIAGIVEEGIPVRRRIPSRTEHNPHNVDYLRTKRERTGHLIELFAEDDDTEAQAG
>NZ_CP017172.1|WP_140798740.1|5276961_5278194_+|molybdopterin-molybdotransferase-MoeA
MNDSATLLPEEDARSQILALCAPLPTEWLLLDDALGRVLAEDVMAQRTLPPWDNSAMDGYAVRSADLAGPLPVRLNVGETIYAGAVGHQALVPGVCARIMTGAPLPAGADAVVMRERTRPVVQSGADQVDVLEAVAPGQFVRPRGEDAREGQLLLARCTPLGIPELGLLWAQGRQAVPVSRAPRVAILSTGDELCHADEPPNGRIVDTNAPSLALAVRRAGGIPTRLGIARDTRDAVLAALSRLDGFDVVLTSAGVSVGERDYVKEVLAELGVEQHFWRVAIKPGKPLVVGRRGATLFFGLPGNPTSSLVTFELFVRPALRKLLGHAQVGPGRVAGRLDGKLSKPSGLAHFVRVTAAWREGSLWARPLATQTSGALRSAAAATHLLHFPREASSLTAGDAVELLPLSWVA
>NZ_CP017172.1|WP_140798739.1|5275386_5276766_-|protease-inhibitor-I42-family-protein
MAKPKSGAKKTTPAGKAGAKPAAKKDSAARLDLIKNASKRVAKAATKLAKAASDVTKGAKSAVKKAVQEKATAKKAAPAGKTASAAKAASPAAKTPKASPAKAPLAAKSAAGAKAGKASAVPAAPPVERPRPRATKLPPPGEPLTKREMEQLLTAGEGRGVTGEGSLKGRLVVTNDMPHLVVVGRDKRELTFLLQGPDQEVLPAYVDHKVSVSGLIRKTTNHAGVVDVRKYSAKKPDSEVVEAAPVETEARLRYLSPGEVSMVTAAGMGAGIKGFAGVRGNLEMTGEEFVLVVSNGGTRQQVSFIIEGKAAGKALRKHVGYTLQVQGVVDKTSGWGGRILAENVELRPSEARAVSRDEMELVHIEGEVPTSVDVRLNHGLAVRLPEHPGFTWAIEPTVAKRVGLREANFEPAPEDGPGTREFFFTPRNPGTFEVEFFLAKALSPGLVDRSFKINVTVKP
>NZ_CP017172.1|WP_140798737.1|5271745_5275279_-|ribonuclease-R
MSLSQDLLKQILAEADHPLGIKELLRLAGLHPGQQTELKRALRELVRQGDILKDGKRFVPRQPSRREADVRAREQGAPMAWRQRDAEGPREGGPGRGPRQAGQRAAGPGGFAARRHEPGARGKRAGWQEQGPGRERKGASKHGGGFRQERGEWPGRRGRFSEVEEDGLLEGILHVHRDGFGFVHPLSGEGDNVFLPPHEAQRALDNDRVVVAVSGRPPRLEGRIVRVVQRRRELAVGTYVVKGRYAVVYPTDSSLPGPIRVPLTQMAREGDLVKVQLGIGAQMLDPDRGLHGEVAGSLGKPGTPSAEVLGVAYSQGFSDEFPPEVMGEADRYAVTVSEEEARGEHRRDLRALPLITIDGEDARDFDDAVYVEDQADGWRLVVAIADVTHYVWEGSALNAEALRRATSVYLPDRVLPMLPERLSNGICSLRPDEDRLCMVADMTFDRRGHRRSYDLYPAVMRSVARCTYNEVQDVLAGKDVPHRNAHKPHFERLMSLARALMKMRKERGAIDFDLPEHKVVLDEEGLPARMDKRERKDSHRLIEECMLAANEAVATFFQDEGLPTVYRFHGEPDPEKLATFAALAEAYGFKMRVEDGVSSKELDAFVSQLQGHPEQRALNQLLLRSMMQAVYTSSRVGHYGLAAEHYLHFTSPIRRYPDLLVHRLLKAHWARKGRKPSQSMLEREEDQLEDMSAQCSERERAAMQVEREVVSFYACLLMKDRVGEEFAATVAAITDFGFFVELDEVHVEGLVKAETLGPGAKLDKLTHSLVYANGRRVRVGQKLRVRLTSVNVTAKKIDFEALQFEGEALLSRVATRGDQPHRRQAWTAEAPSHRERDGRRERAGRPGRREREAAATSQGAPSGHHEETGTGRPRGRFSREGRREEAAPHRKEPRFPPRAPEGQEPPRAESPAWPKRRTFIRPEPQAPAPVSAETAEPLPSEAPSAPASWELPAGDDAARSPHPGFDRIRALASQRQRGPEPRGASHGRSFQKQKPQGGPGPRFPAPKPGRESEDDRAFSIEPPRPPPEAPVEAPPPVPSRAVTETPTPVAPEPVRAAPASVETPVTPAPAPETAAPKRKATRKKAVAKATRTPARKKTTAAGSAKKAAATKAKKPTAKAKKAAPARAAAKATKVAASKSKAKAPSKKAAKPTVARAAKPAKASGAAKKKAPTGRKKR
>NZ_CP017172.1|WP_140792627.1|5271474_5271693_-|DUF3185-family-protein
MSFVRLLGVMLAIAGAVLLWSGLKARDSLAERATELFTGRNTDRTTLYLAGGGAALVGGILMVLAGGGRRRR
>NZ_CP017172.1|WP_140798736.1|5270714_5271458_+|DUF2807-domain-containing-protein
MRIAKSGAWVGTALLAVALTACSSGPFVEGNGRVVESEREIPSFDEVVVNDGISATVVVDPAQPASVIVEGDSNLVSLMRTEVLSGAMLRVHFLADDVGHWESANPLRVRITVPTLTSFQRSGGGTADLSGSIDVPSFLLTASGGGTIRARGFVTERLTLETSGGAETTLEGQATLLDSEMSGGGRLFATGLQTRDARLESSGGGTTEVRVSGSLRVEASGGADIRITGAPTVVEKDLSGGSALRFE
>NZ_CP017172.1|WP_140792623.1|5269753_5270539_+|hypothetical-protein
MKRLGKVGLLVGALTLGGAVVGCKAEDDTAKKHRIVGSDHLSKKEFKEAAAAYALSLQADPKQEKVWEKKAFAHMQLGQMNEAAEAVLKMGEFKTTPTEKAEIYRTLASMYMTGGTTEEAEKYFNEALKLEPKDEASLGWIAEIYAQRGGARSMGAPIIKESLEKSLSYYDQVIAINPNSANTYLNKRVVMGRLMEFERQQKEMALSEATENAKNKEVVAEATARADEHQKRMDEYQVQFAEMTKKFSEAQKAAKAAAPAQ
>NZ_CP017172.1|WP_140800730.1|5268406_5269606_+|metallophosphoesterase
MPVRLFSFSMLIGLGAVLGHLYLYRRLVRPLLPGRLPRLLALAVLVAMTGVLGFRRTVLDLLPESAEGLLTMAVYAWMGVALCLVIALLLTDVGRGLAALARRVRPHASPAPPSPAPSTTVDEDRRRFLGQAVAGSAFVAGGGLATYGSWRAFSPPLVTELAVKIPKLPKALDGLSIVQLTDIHVGHFIQRRYMDALVQQANSLRPDLFAITGDLVDGDVASLGGHVAALAALKSRYGSYFVTGNHDYYSGDEEWSAFLESLGIEVLRNRHVRIGDAGASFDLVGVDDWSGGRRRNKKGYDLDQALAGRAPDRAAVLLAHQPANFKVAAERGVDLQISGHTHGGQLVPMTLLIGLAWEHSAGLYAHGDSNIYVSRGCGFWGPPMRVGSPPELVKLVLTA
>NZ_CP017172.1|WP_140798744.1|5282856_5284113_-|2-oxo-acid-dehydrogenase-subunit-E2
MAIFEFKLPDLGEGVMEGELVKWHVKAGDSVKEDQVLAEVMTDKATVTVPAPKAGRVVKTHGNEGDMAKVHQLLVTLEVEGDAPAQAGGHGEASAPAAAPVAAAGGHGGGAPASASKVLATPVTRRMAREHGLDLAAIAGTGPQGRVTKADVVAALEGGEKNVVAAPAEQKARPAAPAVSSGAADERVPLRGLRKKIAEKMVRSKFTAPHFAFVEEVDATELVALRARLNAQLAAAGENTKLNYLPFIIKATVAALKKFPHLNANFDEASQELVVRGEYNIGMAAATPDGLTVAVVKNADRLTLAELARETARLGAAARDRKLKMEELTGGTFTISSLGQSGGLFATPIINHPEVGILGVHRLKKRPAVVGDQVVVRDMMNLSLSCDHRVIDGSVAADFTYEIIKYLEKPDLLFLAMA
>NZ_CP017172.1|WP_090490647.1|5284173_5285103_-|lipoyl-synthase
MATPDRFPLPQVTETTRKPEWLKVRLPHGEGYERVKAIVKRTKLATVCEEARCPNIAECWGGGTATVMLMGEVCTRACRFCHVKVGAPPPLDPMEPIHLAQAVKEMDLEYIVVTSVNRDDRPDGGASHFASAIRELRRESPRTIVEVLIPDFKGVEKDLTTVAEAKPHVVAHNVETVERLTPTVRDRRAKYHQSLRVLEYLKNRPEGLYTKTSVMVGLGETDAELEQTFKDLRDVGVDVLTLGQYLQPSQYHLRVERFVSPAQFEAYKTLAESYGFLYVASGPLVRSSYRAAEFFMKGLMERERLERLG
>NZ_CP017172.1|WP_140875811.1|5285362_5286760_-|dihydrolipoyl-dehydrogenase
MAETFDVVIIGSGPGGYVGAIRAGQLGLKTAIIEKDKRLGGTCLHRGCIPTKSLLWTAELFHHVREAADFGVDVSSPAINWPNAMKHKDKIVTKGANGIDFLMKKNKVTVVKGHGRIAGKGKVEVTAADGSKQVLEAKNIIIATGSVPKSLPNVPVDHKRVLNSDSILQIDRVPKSIIVLGAGAVGCEFASVFNHVGSKTSIVEYLPALLPIEDADISKELEKIFKRRAIDVHTGSAVEKVEHTADGVRVTMKVGNETKTLEAEILLSAVGRSPVTEDVGLDKTNIQAERGYIKVDSMLRTSEPNVYAVGDIIPTPMLAHMASAECVVAVEHIAGKNPQPINYDLTPSATYCYPEVASVGLTEKKAKERGYDVKVGIAPMGAVTKAAISNEATGMIKIVSDRKYDEVLGVHLIGPHATELLAEACVALKLEITTEELANTIHAHPTLSEIVHEGAEATLGHPRHF
>NZ_CP017172.1|WP_140798745.1|5286777_5287977_+|hypothetical-protein
MRMEPGGADNPRSRLESRSLLVRRFPLRTLLLMLAALIAFGRLWCVTHQEEAPGARPERMAQAGDAPAGAPVPSSAPECLTLERALESALRTPQDTRVLDEARQQLDACRQPPVRACALGVALDARSPLSEGEATPLRGLLTSLCERCPPAANSCARAVGQALLSAAVGSNADIASAKWNLEHAGPGLGGACASLVQLGLAPAAQSDLTVRPPVLALTGELAPRCSQAGFLDDALLRAAAVNLVAPTPALVALAAVPIPPETSAMKPDRIEGTEPGFQAFDRDENTGVPVGKALKSERWAADGALRASYAPTLKQLVSMRIRATGPGTVRAIVRTPEGVGLKDPEKDFAFVNPTVCRFTGTGQWEQCPLQVPLRDVDAVSVFPERADTELKELEVRGAR
>NZ_CP017172.1|WP_140792649.1|5287995_5288445_-|DofB-protein
MNGPTYKAEIIDRVIFSRWENPPTKEDVTLVLAQMQEAATRLNTNLIYVGSVSSKSKVPDANERTVLNQFLMDARRTCVEQAWLIYEGTDLQHNLQRVIISGVLILTRTFDNFLSVAKSGDSIVKDVSAVLKKDAAPLFTMAKERGLVA
>NZ_CP017172.1|WP_140792650.1|5288712_5289321_-|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE
MFDLDALDFAKGNGLVTVVTQDASTGDVLMVAHADREALERTLATGELHYRSRTRGLWHKGATSGNVQRVVALRADCDGDAVLARVEKAGPACHTGTETCFGPGRWDALSALDDTLARRAAPVERPDDAPPSYTRRLLEDRNLRLKKLGEEAAELVTACADADPSRAAEEAADVLYHVLVAVRPLGLSLDDVKAVLARRAPR
>NZ_CP017172.1|WP_140792651.1|5289320_5290100_-|histidinol-phosphatase
MTDSGNLMQAAAEVARMAGDAALGFFRGGIAVDTKSDGSPVTVADRTAESRAREWLEARFPQDGILGEEFGETRPGAKRRWILDPIDGTKTFIRGVPLWGTLVALAEGERILVGAAYFPAVSELLVAAPGQGCFWNDQRAAVSTQAELSQAVVLSTDERFPVYPERGAAWRALARDAAVDRTWGDCYGYLLVATGRAEVMVDELLSPWDGAALQPIIEEAGGVFTDWTGRRTAFGGNGIATNAAMARVVRERLGAVETR
>NZ_CP017172.1|WP_140798746.1|5290096_5290858_-|imidazole-glycerol-phosphate-synthase-subunit-HisF
MLTRRLVVCLDVKGGRVVKGVQFEGLRDVGDPVELARRYEAEGADELTFLDISASAEERDTLWELVRRTAEQLFIPLAVGGGVRTVDDVGRALRAGADKVSINSAAVANPALLTACAERFGAQCVVASIDAKRDGDRWRVYTHGGRKPTDLDAVAWARECVARGAGEVLLTSIDRDGARTGYDLALTRAVSAAVDVPVIASGGAGSAAHVRDAFQEGGADAALVAGILHDGLTTVGAIKALLREGGLHIRSVA
>NZ_CP017172.1|WP_140792654.1|5290857_5291394_-|imidazoleglycerol-phosphate-dehydratase
MTTVIRETKETQVRVELSPGKGVTNVDTGLKFFDHMLATFARYAGLDLSLHARGDLTHHVMEDVAITLGTAVQQVIPATAARFAERTIPMDDALVQACLDAGGRFYYQGPLKNRLYEHWMRSFSEHARVTLHLRVLRGKDSHHATEASFKALGLALRDAMVDSGSVFSMKGAVSLEVK
>NZ_CP017172.1|WP_140792656.1|5291390_5292107_-|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase
MIAIPAIDLREGACVQLVGGSFAAEKVRVEDPLEALKQWRRHGFRAFHVVDLDAALGKGSNSDAIFQLTAYERGLTFSVGGGVRDSDRVEAILSGGAEFVVVGTRAIEDAGWLADIANRFPGRVVVAADVKGREVVTRGWTEGSHRDIREVLAAFKPLPLAGLLVTAVHKEGQLSGVDLPLMREVASTSRHRLYASGGVTTLEDLRALAAAGAYGAVIGMALYTGRLDASAVAREFAG

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_11

5618382-5618517

Orphan

Consensus_repeat	Method
GGGCCGGGAGGACGCGCCATGCCCGGCGGCATCCCAGGTCCCGGGGGACGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_11

>merge|NZ_CP017172|11|5618382-5618517|CRISPRCasFinder
GGGCCGGGAGGACGCGCCATGCCCGGCGGCATCCCAGGTCCCGGGGGACGCGGCGCGCCCGGCGCACCCGGCGGCGGCATGCCTGGGCCGGGAGGACGCGCCATGCCCGGCGGCATCCCAGGTCCCGGAGGACGCG

>NZ_CP017172|11|10|5618382-5618517|CRISPRCasFinder
GGGCCGGGAGGACGCGCCATGCCCGGCGGCATCCCAGGTCCCGGGGGACGCG	GCGCGCCCGGCGCACCCGGCGGCGGCATGCCT
GGGCCGGGAGGACGCGCCATGCCCGGCGGCATCCCAGGTCCCGGAGGACGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140875944.1\|5609661_5610627_-\|class-II-fructose-bisphosphatase	unknown	unknown	gnl\|CDD\|236536
NZ_CP017172.1\|WP_140793060.1\|5610657_5611089_-\|YbgC/FadM-family-acyl-CoA-thioesterase	unknown	unknown	gnl\|CDD\|223894
NZ_CP017172.1\|WP_174258864.1\|5607434_5608505_+\|ADP-ribosylglycohydrolase-family-protein	unknown	unknown	gnl\|CDD\|377122
NZ_CP017172.1\|WP_174259321.1\|5611187_5612801_+\|alkaline-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|293740
NZ_CP017172.1\|WP_140855631.1\|5609194_5609620_-\|SRPBCC-family-protein	unknown	unknown	gnl\|CDD\|176854
NZ_CP017172.1\|WP_140793053.1\|5605263_5606052_-\|5'/3'-nucleotidase-SurE	unknown	unknown	gnl\|CDD\|234732
NZ_CP017172.1\|WP_161606781.1\|5621983_5623501_+\|hybrid-histidine-protein-kinase/response-regulator-SinK	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_002639463.1\|5626569_5626926_-\|response-regulator	unknown	unknown	gnl\|CDD\|381103
NZ_CP017172.1\|WP_140875952.1\|5624757_5626401_-\|chaperonin-GroEL	unknown	unknown	gnl\|CDD\|234573
NZ_CP017172.1\|WP_140875956.1\|5628042_5629020_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187540
NZ_CP017172.1\|WP_174258865.1\|5608604_5608781_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140875948.1\|5613854_5617751_-\|valine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237855
NZ_CP017172.1\|WP_140798910.1\|5612958_5613843_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	unknown	unknown	gnl\|CDD\|238806
NZ_CP017172.1\|WP_011554450.1\|5606056_5607355_-\|phosphopyruvate-hydratase	unknown	unknown	gnl\|CDD\|234617
NZ_CP017172.1\|WP_140875950.1\|5623497_5624580_+\|signal-integration-modulator-SinM	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259322.1\|5627018_5628089_+\|metallopeptidase-family-protein	unknown	unknown	gnl\|CDD\|240572
NZ_CP017172.1\|WP_140798914.1\|5620064_5621438_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP017172.1\|WP_140875958.1\|5629066_5629765_+\|WHG-domain-containing-protein	unknown	unknown	gnl\|CDD\|224228
NZ_CP017172.1\|WP_140793068.1\|5619198_5620014_-\|chemotaxis-protein-CheW	unknown	unknown	gnl\|CDD\|366716
NZ_CP017172.1\|WP_140793072.1\|5621441_5621834_-\|demethoxyubiquinone-hydroxylase-family-protein	unknown	unknown	gnl\|CDD\|275328

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140875944.1\|5609661_5610627_-\|class-II-fructose-bisphosphatase	gnl\|CDD\|236536	PRK09479, glpX, fructose 1,6-bisphosphatase II; Reviewed.	0
NZ_CP017172.1\|WP_140793060.1\|5610657_5611089_-\|YbgC/FadM-family-acyl-CoA-thioesterase	gnl\|CDD\|223894	COG0824, FcbC, Predicted thioesterase [General function prediction only].	1.52043e-41
NZ_CP017172.1\|WP_174258864.1\|5607434_5608505_+\|ADP-ribosylglycohydrolase-family-protein	gnl\|CDD\|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	9.49933e-33
NZ_CP017172.1\|WP_140855631.1\|5609194_5609620_-\|SRPBCC-family-protein	gnl\|CDD\|176854	cd07812, SRPBCC, START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC (SRPBCC) ligand-binding domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket; they bind diverse ligands. Included in this superfamily are the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, and the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), as well as the SRPBCC domains of phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of this 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.	1.73552e-18
NZ_CP017172.1\|WP_140798914.1\|5620064_5621438_+\|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.	4.69321e-55
NZ_CP017172.1\|WP_161606781.1\|5621983_5623501_+\|hybrid-histidine-protein-kinase/response-regulator-SinK	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.62786e-34
NZ_CP017172.1\|WP_140875952.1\|5624757_5626401_-\|chaperonin-GroEL	gnl\|CDD\|234573	PRK00013, groEL, chaperonin GroEL; Reviewed.	0
NZ_CP017172.1\|WP_140875956.1\|5628042_5629020_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187540	cd05229, SDR_a3, atypical (a) SDRs, subgroup 3. These atypical SDR family members of unknown function have a glycine-rich NAD(P)-binding motif consensus that is very similar to the extended SDRs, GXXGXXG. Generally, this group has poor conservation of the active site tetrad, However, individual sequences do contain matches to the YXXXK active site motif, and generally Tyr or Asn in place of the upstream Ser found in most SDRs. 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.	4.56131e-104
NZ_CP017172.1\|WP_174259321.1\|5611187_5612801_+\|alkaline-phosphatase-family-protein	gnl\|CDD\|293740	cd16016, AP-SPAP, SPAP is a subclass of alkaline phosphatase (AP). Alkaline phosphatases are non-specific phosphomonoesterases that catalyze the hydrolysis reaction via a phosphoseryl intermediate to produce inorganic phosphate and the corresponding alcohol, optimally at high pH. Alkaline phosphatase exists as a dimer, each monomer binding 2 zinc atoms and one magnesium atom, which are essential for enzymatic activity. Although SPAP is a subclass of alkaline phosphatase, SPAP has many differences from other APs: 1) the catalytic residue is a threonine instead of serine, 2) there is no binding pocket for the third metal ion, and 3) the arginine residue forming bidentate hydrogen bonding is deleted in SPAP. A lysine and an asparagine residue, recruited together for the first time into the active site, bind the substrate phosphoryl group in a manner not observed before in any other AP.	4.9294e-85
NZ_CP017172.1\|WP_140875948.1\|5613854_5617751_-\|valine--tRNA-ligase	gnl\|CDD\|237855	PRK14900, valS, valyl-tRNA synthetase; Provisional.	0
NZ_CP017172.1\|WP_140798910.1\|5612958_5613843_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	gnl\|CDD\|238806	cd01572, QPRTase, Quinolinate phosphoribosyl transferase (QAPRTase or QPRTase), also called nicotinate-nucleotide pyrophosphorylase, is involved in the de novo synthesis of NAD in both prokaryotes and eukaryotes. It catalyses the reaction of quinolinic acid (QA) with 5-phosphoribosyl-1-pyrophosphate (PRPP) in the presence of Mg2+ to produce nicotinic acid mononucleotide (NAMN), pyrophosphate and carbon dioxide. QPRTase functions as a homodimer with two active sites, each formed by the C-terminal region of one subunit and the N-terminal region of the other.	3.58069e-128
NZ_CP017172.1\|WP_011554450.1\|5606056_5607355_-\|phosphopyruvate-hydratase	gnl\|CDD\|234617	PRK00077, eno, enolase; Provisional.	0
NZ_CP017172.1\|WP_002639463.1\|5626569_5626926_-\|response-regulator	gnl\|CDD\|381103	cd17551, REC_RpfG-like, phosphoacceptor receiver (REC) domain of cyclic di-GMP phosphodiesterase response regulator RpfG and similar proteins. Cyclic di-GMP phosphodiesterase response regulator RpfG, together with sensory/regulatory protein RpfC, constitute a two-component system implicated in sensing and responding to the diffusible signal factor (DSF) that is essential for cell-cell signaling. RpfC is a hybrid sensor/histidine kinase that phosphorylates and activates RpfG, which degrades cyclic di-GMP to GMP, leading to the activation of Clp, a global transcriptional regulator that regulates a large set of genes in the DSF pathway. RpfG contains a CheY-like receiver domain attached to a histidine-aspartic acid-glycine-tyrosine-proline (HD-GYP) cyclic di-GMP phosphodiesterase domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.45051e-26
NZ_CP017172.1\|WP_174259322.1\|5627018_5628089_+\|metallopeptidase-family-protein	gnl\|CDD\|240572	cd12952, MMP_ACEL2062, Minimal MMP-like domain found in Acidothermus cellulolyticus hypothetical protein ACEL2062 and similar protein. The subfamily includes an uncharacterized protein from Acidothermus cellulolyticus (ACEL2062) and its homologs from bacteria. Although its biological role remains unclear, ACEL2062 contains a minimal metalloprotease (MMP)-like domain consisting of 3-stranded mixed 2-beta sheets and a HExxHxxGxxD/S (x could be any amino acid) motif. It may belong to a superfamily of bacterial zinc metallo-peptidases, which is characterized by a conserved HExxHxxGxxD motif.	7.86162e-35
NZ_CP017172.1\|WP_140875958.1\|5629066_5629765_+\|WHG-domain-containing-protein	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.57566e-14
NZ_CP017172.1\|WP_140793068.1\|5619198_5620014_-\|chemotaxis-protein-CheW	gnl\|CDD\|366716	pfam01584, CheW, CheW-like domain. CheW proteins are part of the chemotaxis signaling mechanism in bacteria. CheW interacts with the methyl accepting chemotaxis proteins (MCPs) and relays signals to CheY, which affects flageller rotation. This family includes CheW and other related proteins that are involved in chemotaxis. The CheW-like regulatory domain in CheA binds to CheW, suggesting that these domains can interact with each other.	1.04319e-06
NZ_CP017172.1\|WP_140793072.1\|5621441_5621834_-\|demethoxyubiquinone-hydroxylase-family-protein	gnl\|CDD\|275328	TIGR04535, conserved_hypothetical_protein, ferritin-like protein. Two families of proteins are known to be encoded, with some regularity, next to the gene for encapsulin (pfam04454), with surrounds the target protein to form a prokaryotic proteinaceous organelle. One is the family of enzymes that includes Dyp-type peroxidases. The other is this family, with a resemblance to bacterioferritins. Encapsulin-associated forms of the proteins in these two families have a necessary C-terminal motif that resembles DGSL[SGN]IGSL[KR]. Members of this family that include the last columns of the model in the hit region (and are encoded next to the encapsulin gene) should be designated encapsulin-associated ferritin-like protein.	1.03724e-19
NZ_CP017172.1\|WP_140793053.1\|5605263_5606052_-\|5'/3'-nucleotidase-SurE	gnl\|CDD\|234732	PRK00346, surE, 5'(3')-nucleotidase/polyphosphatase; Provisional.	1.9791e-132

>NZ_CP017172.1|WP_140875948.1|5613854_5617751_-|valine--tRNA-ligase
MTDTTELSKAYEPTEVEARRYAFWLERNYFRAEAPSDKPPFSIVLPPPNVTGSLHIGHALTATIQDILTRWKRMSGFNALWLPGTDHAGIATQMVVERELKATEGKSRHDLGREAFLERVWEWKGKFGARIGEQHRYLGASLDWSRERFTMDEQSSAAVREVFVRLYEEGLMYRAQKLINWCPSCRTALSDLEVEHQEKNGSIWHIRYPVKDSDRTLTVATTRPETMLGDTAVAVHPEDERYQDLIGKHVVLPLSGREIPIIADGELVDPKFGTGVVKVTPAHDFNDYQTGLRHKLPMLSILDESARMTKETGKYAGLDRFEARKQVLADLQEQGLLEKEEPHKLSVGTCQRSATVVEPRLSPQWFVKIEPLAKPAIEAVEQGRTKFVPESWTNTYFHWMRNIHDWCVSRQLWWGHQIPAYYCTACSPRLGDDTDLPLDAATVKVGGVDFARAEPIVAREQPSACPKCGGATFIQDPDVLDTWFSSALWPFSTLGWPRNTPDLQTFYPTSVMETGHDIIFFWVARMMMMGLHFMGDVPFRTVYLHAMVRDEKGEKMSKTKKNVIDPLDVILGAPADKLEPTLRNKFPQGMPAFGADALRFTLASLTQQGRDIKLSMDRMAGYKAFCNKLWNASRFALMNMGEFTLDERPLKERPLTLADRWILSRLQRATTEARASLETYGFAEAASTLYQFLWAEFCDWYIELAKGSLYGTDEQAKDSARAVLVYSLDRILRLLHPFMPFITEEIWQKLPMSRSVDSIMIASYPEPDADLVDEAAEAEMAPVIATIEGLRTIRGESNLSPATKVKAVVQSPDARTRELLERWRAYLMPLAGLSEVEIGAPGTKPPQAAAFVGTNLEIYVPLAGLIDLDAERDRLRKEIARAEQEAAGVLRKLENPNFVAKAPPDVVEKDRARVEELKERKAKLQDHLQRIAPEPAMPAAPPSESSTPTESVEPTEADIATEADVATEPITPPESAASLETRPPVEGGTEYETLAESTEEEEASTVPAEVKVAPDAEAEGNVDLAEELKDELEAAGGVTEAADPQVQEALEKLRAGTKEGLSPADHHDLGVAYMSMGLVDDAMREFNTARAGGDAREVPAAAKQEAAESEQTVASTAKAVVKAALAAVKKASSIAKEAVSASDEEPAAPAKARPAKKAAGKKAAVTKAAGAKGAAKKGAAKKAPAKGAAKKASAQKAAAKKAPAKAASKKASAQKAAAKKAPAKGAAKKAAAKKAPAKVAAKKAATKKGAAKKVAAASKKPVKKAAGRKAPAKKAPASKAAAKKGTGAKPKARAKARR
>NZ_CP017172.1|WP_140798910.1|5612958_5613843_-|carboxylating-nicotinate-nucleotide-diphosphorylase
MQQQDYLDRLIALALDEDLGAAGDVTSQALIPPDYEGSAELVAKEQLVLAGLDAFVRVFKTVDPNVEVELLRRDGQEIKPKMVAARCHGRMRSLLAAERTALNIVQRAAGIATLAQQAVTSVRGSNLRVLDTRKTPPGMRTVAKEAVRMGGASNHRFGLFDGVLIKDNHIAAVGGSIAEALRRAKLNGPRLTKIEIEVTNLKQLAEAIEHGADVVMLDNMDDAQIREAVKLAAGRVPLEVSGGVTLDRLPRLAKLGIDFVSMGALTHSARAMDLSLEITAAAKRPARSKQPKPA
>NZ_CP017172.1|WP_174259321.1|5611187_5612801_+|alkaline-phosphatase-family-protein
MIRALVLAVALATLPAFARPPRLTLVISVDALGSDVLLRNRPRLKGGLGQLLNQGAYFPYARYGYAECRTAPGHATLSTGANPWRHGIVDNRWVDRSTMKRVMSFADAAHPVLEVPLKPGQDSGPAHLMVETLADRLRVTTQERGKAVALAIKPHASIALAGRAGQAWWFDKGEGKFVTGTWYTKEFPAWLKALNARKLPEASFGKKWELMRPASEYVGEDEGLAESDVYGLGRTFPHPLDGGLPSPGPTFYQAFAVSPDSHDLLVEAAKAAIAGEGLGQDDVPDLLAVSFSGTDLVFHEYGPYSWEMQDTLLRLDKAMGNLIAAAERAAGGRGNLVIALSADHGGAAMPEQWAAKGLPAKRVTSAELAEGLTQALRQQFGGDVTATLEQLDVYLGGQTHQGGAVDSAVRRAAAAWLAKHPSVITAVANDDLFTAPDTAGYLASMRKSYYPGRSGDVLFMIRPFHLLHYIPTGTSHGTPHSYDSQVPILFAGKGVKPGMYLEEIDPVDFAPTLSALMEMGMPASAEGKPRSEVLTGK
>NZ_CP017172.1|WP_140793060.1|5610657_5611089_-|YbgC/FadM-family-acyl-CoA-thioesterase
MVEARLRVIYGDTDQMGVVYYANYFRYFEFARSEYFRARGGSYAELERSGALLPVAEASCQYKASARYDDLLVIQTTVSELRRASIVFTYALFRDGAPRTLLCTGMTRHACVGRDGKPTRLPDSLIRLLETTEPSPGSSTSST
>NZ_CP017172.1|WP_140875944.1|5609661_5610627_-|class-II-fructose-bisphosphatase
MDRNLAMEVVRVTEMAAIASARLMGRGNKDESDQAAVDAMRRAFDALQIDGTVVIGEGERDEAPMLYIGEKVGKRGEGAPEVDIALDPLEGTNLCAYGRPGSIAVVAMAGKGGLLNAPDTYMEKMAVGPRARGAIDLRKTPTENLRSIAEKMKVYVEDLTVVVLDRERHTDLIKEIRAAGARIRLIEDGDVAGAIATCFEDTGVEVLMGIGGAPEGVIAAAAIRATGGDMQGRLVPRNQGEIDRAKSMGITDISKIYTAEELAKGEVMFAATGVTTGDFLKGVRFFGGGCETHSVVMRSKTGTVRFIQSVHKFDKKPGYAF
>NZ_CP017172.1|WP_140855631.1|5609194_5609620_-|SRPBCC-family-protein
MPGASRTIIVNAPIEKVFDVITQYERYPEFLPEVKGIRTENRKGNTVDVHYKVDVLKTINYSIHVTEERPTRMSWSYIKGEFMKDNQGSWVLEPEGEGKTKATYTVEMALGALVPKSVVSALVETSLPKMLDAFKRRFEAP
>NZ_CP017172.1|WP_174258865.1|5608604_5608781_-|hypothetical-protein
MLDAFIIEEIKRRERRREEHDRPVVELPLPVPDDRPRRRTETEDDKPQRGVVVIDLLA
>NZ_CP017172.1|WP_174258864.1|5607434_5608505_+|ADP-ribosylglycohydrolase-family-protein
MPPPQRRPTLKGPDPLLAQRRRGALLGMAVGNALSVPTAHRPFMAVPFPKQAEGPYMKLMGGGPHELRRGQVTEEVQLAACLSHSLRSIKRYDAADALRRYRAWQPHAFDVSEPMKEVFEDCQTSGFPPLGAGMRVWLRAYRKPADPGSLARAAPLGVYLAGDAHALTQASLEDSALTHFDPRCQLACAAFNAAIGHAVTHGAGLKAADLIPAAESGLLLAGAALGRSASDYVQEVSFAASLLREDLAIAQQEDPMLYGPELHLHRPLHAVRVAFRLAFWELLHAPSAEAALLDVVHRGGDTEAHATITGALVGAFHGEQALPEEWRKQVLEALATVKGPLWDVYHPRHLLALTNA
>NZ_CP017172.1|WP_011554450.1|5606056_5607355_-|phosphopyruvate-hydratase
MTEISQILAREVLDSRGNPTVEAEVQLAGGARGRAAVPSGASTGEHEAIELRDGDKHRYLGKGVQKAVKNVVDVLAPALVGMDAADQFAVDQRMLELDGTATKGKLGANAILAVSMAAARAAADAHGLPLYRYVGGVQARTLPVPLMNILNGGAHADTRVDVQEFMVVPAGASSFAEGLRWGAEVFHALKKILKGRKLATGVGDEGGYAPDLPANEEALKLIMEAIDQAGFKAGEQLFLALDVAASEFFDKGSKKYKLKGEGKEYDSTGLLEYYRGLSERYPIISIEDGMAEDDWEGWKKLTDALGSRMQLVGDDLFVTNVERLGRGIETGTANSILVKVNQIGTLTETFDAVRMAHRAGYTSVMSHRSGETEDTTIADLAVALDCGQIKTGSASRSDRVAKYNQLLRIEGELGAAARYAGKSVFRALNQKK
>NZ_CP017172.1|WP_140793053.1|5605263_5606052_-|5'/3'-nucleotidase-SurE
MSDKPKRILVSNDDGYFSEGLQALVEAVSPLGEVWVVAPDREQSAASHAISLHRPLRIKEVRARWFAVDGTPADCAYLAINHLLKDDRPVLMVSGINHGANLAEDIMYSGTVAAAMEGALLGVPAIAFSLVARRNFDFAPAARFARSLVSSALSRPLPPRMLLNVNIPGGVEPEGYAITRQGRHSYGFEVVENEDPRGRKYYWIGGSDYQHEDIPGSDCNAVFRDKRVSVTPLHFELTDHGRLPDLSGWQVDGFNRHEPDGA
>NZ_CP017172.1|WP_140793068.1|5619198_5620014_-|chemotaxis-protein-CheW
MSPFESGRRLCLLVEAGETRYAVEATSVMEVAMPGANGSSLRGVLEVKDLCALLGGPPEEGPGMVVVLDVSPTLAVRVRSVVEVADVARAPFFLLPPGLADSLAPLSRGAVLHKSRLYLELIAEALPHRVGSMSAAVAARPVHWAEAAPDRALVFESQSRLFGVPLGLVSQVISRGEAFSVLPVQSGPVAGIFPHDQVLWPVCSVPALLGESPVPEPFIVLTELAGRNVGLTATRVLGVMQRFEPDDTAGSFRAPGLSEPVAFLDLQRMFS
>NZ_CP017172.1|WP_140798914.1|5620064_5621438_+|diguanylate-cyclase
MARILLVDDEKIARTLYGDYLTAVGHAVTAVGTLQEAKEALAGDRFDAVVTDLILPGGDGMEVLRHVREHHPGVEVVVITGLEKVDPAVRAIKSGAAEYLVKPVAPEALQHAVRRALTTRDLMQENASLRRHVAMLEAGQRIATTLDREKLAAVTASALQSMASASAVVLLERDSAFALRRHGTSGLSTALEEPLIAELIERLSNERGPRELDGLDAPFPRAVSFPALEGEAVLGHAVLFFGGTGAEWAGETASFLVRNWALALRNLGRFAAVEDLAYVDDLTRLFNTRYLHLVVDREVQDALQSQRTFSLLFLDLDHFKSINDTHGHLVGSKVLVEAARVVKGCVRDHDVVARYGGDEYVVVLRNTDSGGALKVAERIRRTMETHNFLAREGLSLKLTTCIGVASFPEHAQDKATLLDLSDRAMYRGKRGSRNVVYMAAKDLEAPPAERRQAHSAS
>NZ_CP017172.1|WP_140793072.1|5621441_5621834_-|demethoxyubiquinone-hydroxylase-family-protein
MPQTNPFHSLVPRKMTDSELARSIRLNIEAELDAINLYAAHIDATDNEDAKAILQHVMDEEREHAALFWELIARLDPEQAAHAKEAVEKYRLITSGASHEAVEAVGKEGAAPAPADVTPEKRLTVGSLRR
>NZ_CP017172.1|WP_161606781.1|5621983_5623501_+|hybrid-histidine-protein-kinase/response-regulator-SinK
METPAPLAQLLQAVEAGDLTAARTAAAALQRAGAHTSQLAAEVLHELRQPLLGVKAYAQLLAEDGAAPGPLRLLLAQVERMEQIVSDFIRLSSERPASQQRLSLAAPIWAAAKHFSINPDSSRISLEVEAPEDITIQGNARLIEQLTLNLLNNARDAMAGRGRVKVVLTKEGPSPALYVADWGPGIPEELRARIFEPYITANKRGTGLGLSVCQRIAREHHARLELAPQGVIRDVPPPATVFRVLFPATDAPPTQKHRVLVVDDEIIIRMVFRDLMGKECEIIEAESGEEALDLLQQAPVDLIVTDKNLPGMSGLELAQQARRLHTDSRVILMTGYPSLVTTQQALELGVVDYLLKPFDDIREVRALLRSTLAWKPVPAPLATNPAMRRVDVLEDNPAAAAQITHALSLVGLEARILTTTELAALEPPAGVVVSWDFTPAYGRKALELGKALAQGAPFVVLAEHLTMETALESLRAGAAACLPKLMSDASALSRELNRAFKRETP
>NZ_CP017172.1|WP_140875950.1|5623497_5624580_+|signal-integration-modulator-SinM
MRLALLSVLLLGVACSSDKPPTQDGPDAGRGDAGTGTDDAGSGDAGCEPLASGPGTPLLTGLNTPRRLAADETDLYIAESHSLNPQQPQPGPGRLLRLPRAGGDAVSVATGFRAPDAIAVVSDSVYVLDLDGLWRVDKATGAKDARPLDATVNNVTIGGTEVLPARMGDRDVVVIATSHRRLVRVDASGGNRQELYAGTGYTQVRGARVLGQDVWFLVAAGESPGLYSVPLDGSAPATLRDGSITAGTSLEVTPTHFLVTEGGSGNGRVLRLPREGGAAEVVATNLQGPAFPVELNGTLYFKDVSTGGTDFLRRVSTCTSGALEPVGPEGVGPGGLLVDGDTLLYTSQESGTGGFVGRVP
>NZ_CP017172.1|WP_140875952.1|5624757_5626401_-|chaperonin-GroEL
MAAKEIFFHQSAREAILRGVRTLSDAVAVTLGPKGRNVVIEKSFGSPTITKDGVTVAKEIDLENKFENMGAQMVKEVASKTSDKAGDGTTTATVLARAIYEEGLKLVAAGHSPMDLKRGIDKAVEVVVGELKSLSKPTADKKAITQVGTISANGDETIGAIIADAMEKVGKEGVITVEEAKGLETTLDVVEGMQFDRGYVSPYFVTNRERMEAVLDDPYILISEKKVSSMQDMIPLLEQVARSGKPLIIIADDIEGEALATLVVNKIRGVLNVCAVKAPGFGDRRKEMLQDIAVLTGGTVVSEDLGHKFETLTLTDLGRAKRVTVDKDNTTVVDGVGTKATIEGRIKLIRTQIDTVTSDYDREKLQERLAKLVGGVAVINVGAATETEMKEKKARVEDALHATRAAVEEGIVPGGGVAYLRALPALEKLKLGGEQDFGVAIILRALQEPLRKIASNAGVEGAVVINKVREGTGAFGYNARTEVYEDLEKAGVIDPTKVERTALQNAASVASLLLTTEAMVAERPKGKSKGGGAGSSMPDYGGDDMDY
>NZ_CP017172.1|WP_002639463.1|5626569_5626926_-|response-regulator
MNILVVDDDLELCTMLSRFLEMHGFTVYSASDALQALDVLERNQVSMVITDYVMPHMDGIQFTEMLKADPRFQSVPVLLMTGSEDGSVTDRGLRKGVALTLHKPLDMGQLLTLVRFAQ
>NZ_CP017172.1|WP_174259322.1|5627018_5628089_+|metallopeptidase-family-protein
MGTRTSKRTGAGGMEALDAAAEAFERGDFEAALAAADRVLAQASDALDALHLRAAALVELGRLEEAGRAFGAALRVSPDDLEVLLGTADLLICRVGEDREAVEEGLGFCAKGKRLAQKAGDVEVLYEFLLLEGMGLNQVGDCRTALASLDAALGHMPRSVDAQLERGIALFELCRFDEAKAAFDKVLKDTPDEAWAHQYVGLLAERRGDEKEAQRRFAKAQALVPTEFFPPVELGEAEFDRAVEAAVQSLPGHAKQYLDNVTIAVEDLPADEDLLGEDPPLSPSILGVFRGLAVGERSVTNAFDHVPASIVLYQKNLERFARSREELIEQIGITVMHEVGHLMGLDEDDLWQRGLD
>NZ_CP017172.1|WP_140875956.1|5628042_5629020_-|NAD-dependent-epimerase/dehydratase-family-protein
MGTVALFGASGVVGHSIAQTLRGQGRGYRVVGRSREGLQREFGADPQAEIVTWNPDDMASIQAAARGVQTLVYLVGVPYWQFHLHPELMKRTLDAAIAEGVERIVFIASVYPYGRPRTDVVNESHPRVPHTNKGRLRKAQEDLLLAADKAGSIKVTILRLPDFYGPGVENSFLHRAFVAASQGKRAQLIGPIDTPHEFVYVPDVGPTVTALMGSPGAYGRFWNLGGAGVTSQAALVEDIYAQAGHPAKYSVLGPGMVRVLGLFSPFMRELGEMHYLHTSPVIMDDSALRALLGDIRKTPYRDGIRQTLAALSPAPVATGHPHPVP
>NZ_CP017172.1|WP_140875958.1|5629066_5629765_+|WHG-domain-containing-protein
MNTVHLLLAVQLVKAYTGNMGIAERKERQRAELREQILRVARDIVVKEGFPALSMRKLADAVEYAPATLYLHFENREAIAKELCVRGFQDLLAMLEPAAQVEDPLERLPKLAEAYVRFGLEHPETYRLIFMEDPKLSTALFGDHPEGAGPRSFGVLVQVFVDLLEAERLEEGTRPDQLAEVLWAGVHGIVSLRLTCTGFPGTPAEELTQLLVTTLVKGLPGLKARRAQKKAQ

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_12

6524580-6524670

Orphan

Consensus_repeat	Method
CCCGCGAGCCGCCGCATGGGCTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_12

>merge|NZ_CP017172|12|6524580-6524670|CRISPRCasFinder
CCCGCGAGCCGCCGCATGGGCTGAGCCCGGCGCATCAAGATGCGCTGACGCCGGCACCACCACCCTCGCCCACGAGCCGCCGCATGGGCTG

>NZ_CP017172|12|11|6524580-6524670|CRISPRCasFinder
CCCGCGAGCCGCCGCATGGGCTG	AGCCCGGCGCATCAAGATGCGCTGACGCCGGCACCACCACCCTCG
CCCACGAGCCGCCGCATGGGCTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140794231.1\|6523147_6524533_+\|thiol-oxidoreductase	unknown	unknown	gnl\|CDD\|226019
NZ_CP017172.1\|WP_140856162.1\|6532647_6533199_-\|RNA-polymerase	unknown	unknown	gnl\|CDD\|132044
NZ_CP017172.1\|WP_140794240.1\|6534469_6534904_-\|arginine-repressor	unknown	unknown	gnl\|CDD\|224355
NZ_CP017172.1\|WP_174259070.1\|6517504_6517999_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794226.1\|6516545_6516860_+\|DUF1844-domain-containing-protein	unknown	unknown	gnl\|CDD\|378088
NZ_CP017172.1\|WP_140876493.1\|6535073_6536081_+\|N-acetylornithine-carbamoyltransferase	unknown	unknown	gnl\|CDD\|235304
NZ_CP017172.1\|WP_140876483.1\|6516168_6516549_+\|RNA-polymerase-subunit-sigma	unknown	unknown	gnl\|CDD\|368199
NZ_CP017172.1\|WP_140794236.1\|6531226_6531643_-\|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224647
NZ_CP017172.1\|WP_140876487.1\|6527508_6528819_+\|amidohydrolase	unknown	unknown	gnl\|CDD\|349914
NZ_CP017172.1\|WP_140876491.1\|6533508_6534318_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140856150.1\|6521665_6522682_+\|MsnO8-family-LLM-class-oxidoreductase	unknown	unknown	gnl\|CDD\|274646
NZ_CP017172.1\|WP_140794228.1\|6518267_6520892_+\|ATP-dependent-chaperone-ClpB	unknown	unknown	gnl\|CDD\|274529
NZ_CP017172.1\|WP_140876479.1\|6514634_6515399_-\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|224982
NZ_CP017172.1\|WP_140876481.1\|6515419_6516076_-\|thiamine-phosphate-synthase	unknown	unknown	gnl\|CDD\|234590
NZ_CP017172.1\|WP_140794227.1\|6516856_6517498_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794242.1\|6536124_6537051_+\|acetylglutamate-kinase	unknown	unknown	gnl\|CDD\|239783
NZ_CP017172.1\|WP_140856148.1\|6520971_6521655_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223498
NZ_CP017172.1\|WP_140876485.1\|6526039_6527368_-\|DUF418-domain-containing-protein	unknown	unknown	gnl\|CDD\|225193
NZ_CP017172.1\|WP_140876489.1\|6528950_6531170_+\|putative-Ig-domain-containing-protein	unknown	unknown	gnl\|CDD\|310150
NZ_CP017172.1\|WP_174258896.1\|6531744_6532599_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187578

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140794231.1\|6523147_6524533_+\|thiol-oxidoreductase	gnl\|CDD\|226019	COG3488, COG3488, Predicted thiol oxidoreductase [Energy production and conversion].	1.57718e-148
NZ_CP017172.1\|WP_140856162.1\|6532647_6533199_-\|RNA-polymerase	gnl\|CDD\|132044	TIGR02999, Sig-70_X6, RNA polymerase sigma factor, TIGR02999 family. This group of sigma factors are members of the sigma-70 family (TIGR02937) and are found in a variety of species including Rhodopirellula baltica which encodes a paralogous group of five.	1.58272e-66
NZ_CP017172.1\|WP_140794242.1\|6536124_6537051_+\|acetylglutamate-kinase	gnl\|CDD\|239783	cd04250, AAK_NAGK-C, AAK_NAGK-C: N-Acetyl-L-glutamate kinase - cyclic (NAGK-C) catalyzes the phosphorylation of the gamma-COOH group of N-acetyl-L-glutamate (NAG) by ATP in the second step of arginine biosynthesis found in some bacteria and photosynthetic organisms using the non-acetylated, cyclic route of ornithine biosynthesis. In this pathway, glutamate is first N-acetylated and then phosphorylated by NAGK to give phosphoryl NAG, which is converted to NAG-ornithine. There are two variants of this pathway. In one, typified by the pathway in Thermotoga maritima and Pseudomonas aeruginosa, the acetyl group is recycled by reversible transacetylation from acetylornithine to glutamate. The phosphorylation of NAG by NAGK is feedback inhibited by arginine. In photosynthetic organisms, NAGK is the target of the nitrogen-signaling protein PII. Hexameric formation of NAGK domains appears to be essential to both arginine inhibition and NAGK-PII complex formation. NAGK-C are members of the Amino Acid Kinase Superfamily (AAK).	5.76021e-100
NZ_CP017172.1\|WP_140794226.1\|6516545_6516860_+\|DUF1844-domain-containing-protein	gnl\|CDD\|378088	pfam08899, DUF1844, Domain of unknown function (DUF1844). This family of proteins are functionally uncharacterized.	3.68993e-30
NZ_CP017172.1\|WP_140876493.1\|6535073_6536081_+\|N-acetylornithine-carbamoyltransferase	gnl\|CDD\|235304	PRK04523, PRK04523, N-acetylornithine carbamoyltransferase; Reviewed.	2.33186e-171
NZ_CP017172.1\|WP_140876483.1\|6516168_6516549_+\|RNA-polymerase-subunit-sigma	gnl\|CDD\|368199	pfam04931, DNA_pol_phi, DNA polymerase phi. This family includes the fifth essential DNA polymerase in yeast EC:2.7.7.7. Pol5p is localized exclusively to the nucleolus and binds near or at the enhancer region of rRNA-encoding DNA repeating units.	8.11741e-08
NZ_CP017172.1\|WP_140794236.1\|6531226_6531643_-\|winged-helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	4.67899e-37
NZ_CP017172.1\|WP_140876487.1\|6527508_6528819_+\|amidohydrolase	gnl\|CDD\|349914	cd05664, M20_Acy1-like, M20 Peptidase aminoacylase 1 subfamily. Peptidase M20 family, Uncharacterized subfamily of proteins predicted as putative amidohydrolases or hippurate hydrolases. These are a class of zinc binding homodimeric enzymes involved in the hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in the protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. Aminoacylase 1 (ACY1) breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as in the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine).	0
NZ_CP017172.1\|WP_140794240.1\|6534469_6534904_-\|arginine-repressor	gnl\|CDD\|224355	COG1438, ArgR, Arginine repressor [Transcription].	2.3624e-26
NZ_CP017172.1\|WP_140856150.1\|6521665_6522682_+\|MsnO8-family-LLM-class-oxidoreductase	gnl\|CDD\|274646	TIGR03558, oxido_grp_1, luciferase family oxidoreductase, group 1. The Pfam domain family pfam00296 is named for luciferase-like monooxygenases, but the family also contains several coenzyme F420-dependent enzymes. This protein family represents a well-resolved clade within family pfam00296 and shows no restriction to coenzyme F420-positive species, unlike some other clades within pfam00296. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP017172.1\|WP_140794228.1\|6518267_6520892_+\|ATP-dependent-chaperone-ClpB	gnl\|CDD\|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP017172.1\|WP_140876479.1\|6514634_6515399_-\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	gnl\|CDD\|224982	COG2071, COG2071, Predicted glutamine amidotransferases [General function prediction only].	5.1806e-81
NZ_CP017172.1\|WP_140876481.1\|6515419_6516076_-\|thiamine-phosphate-synthase	gnl\|CDD\|234590	PRK00043, thiE, thiamine phosphate synthase.	1.99965e-69
NZ_CP017172.1\|WP_140856148.1\|6520971_6521655_+\|hypothetical-protein	gnl\|CDD\|223498	COG0421, SpeE, Spermidine synthase [Amino acid transport and metabolism].	3.92554e-20
NZ_CP017172.1\|WP_140876485.1\|6526039_6527368_-\|DUF418-domain-containing-protein	gnl\|CDD\|225193	COG2311, COG2311, Predicted membrane protein [Function unknown].	2.05194e-63
NZ_CP017172.1\|WP_140876489.1\|6528950_6531170_+\|putative-Ig-domain-containing-protein	gnl\|CDD\|310150	pfam05345, He_PIG, Putative Ig domain. This alignment represents the conserved core region of ~90 residue repeat found in several haemagglutinins and other cell surface proteins. Sequence similarities to (pfam02494) and (pfam00801) suggest an Ig-like fold (personal obs:C. Yeats). So this family may be similar in function to the (pfam02639) and (pfam02638) domains. This domain is also found in the WisP family of proteins of Tropheryma whipplei.	2.81218e-05
NZ_CP017172.1\|WP_174258896.1\|6531744_6532599_+\|SDR-family-oxidoreductase	gnl\|CDD\|187578	cd05269, TMR_SDR_a, triphenylmethane reductase (TMR)-like proteins, NMRa-like, atypical (a) SDRs. TMR is an atypical NADP-binding protein of the SDR family. It lacks the active site residues of the SDRs but has a glycine rich NAD(P)-binding motif that matches the extended SDRs. Proteins in this subgroup however, are more similar in length to the classical SDRs. TMR was identified as a reducer of triphenylmethane dyes, important environmental pollutants. This subgroup also includes Escherichia coli NADPH-dependent quinine oxidoreductase (QOR2), which catalyzes two-electron reduction of quinone; but is unlikely to play a major role in protecting against quinone cytotoxicity. Atypical SDRs are distinct from classical 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.	1.14145e-88

>NZ_CP017172.1|WP_140794231.1|6523147_6524533_+|thiol-oxidoreductase
MRRRLYLLGIPVGALALAAVWAGTHQQPPPLELGALPTTAEPGEELSGGRGSVPDPGRNAFGRSPMNMPRTRWEDFHAGKRVFGRDWTDVDGPIQVGPLFNAPSCMTCHVKDGRGQPPASPSETPVSLAFQLSGPDGRGPHPVYGAQLDVRHVDGAGAEGSVKVTYEKVTGRFATGESFTLHRPRYQFTGLSKGPIGEGTRFSPRVAPANHGLGLLEAIPESALLAHEDVEDRDQDGISGRANRVKDAATGQTRLGRFGWKANQPTLHQQVAHALVTDMGLTTELFPREQGREAHDAVPPEVSPQELASLLIYARLVAVPKRRDWEAADVLRGKAVFSAIGCTGCHVATPFATEDVPGFPELSGQLIRPFTDLLLHDMGEGLADDRPDGLASGTEWRTPPLWGIGLVKAVNGHTRFLHDGRARNLEEAVLWHGGEAAPAQERYTRLPPTDRQALLAFLGSL
>NZ_CP017172.1|WP_140856150.1|6521665_6522682_+|MsnO8-family-LLM-class-oxidoreductase
MIPFSVLDLSPVTQGSTAADALRNTLDLARHAEDWGFKRFWLAEHHNMTGIASAATSVVIGYVAGGTKRIRVGSGGVMLPNHAPLIIAEQFGTLETLYPGRIDLGLGRAPGTDMLTARALRRDLAASADTFPQDVVELKSFFEPTEPGQLIQAVPGAGLKVPIWLLGSSLFSAQLAAMLGMPFAFASHFAPDALLQALDIYRERFKPSESLERPYAMACVNVFAADTDAEAQRLFTSVQQQFIRLRRGTPGQLPPPVDDIDSVASPVDRASADHALKYSIIGAPDTVQQGLASFIRLTGVDELMVTGMVYDHAARLRSFELTAQAHKKLSEAEAARTA
>NZ_CP017172.1|WP_140856148.1|6520971_6521655_+|hypothetical-protein
MKPWETLERAEVPDVGEITLARRGDEYIFRVRGQTLMSSRQHGSEEALADAGCEGLAGRSGVRVLVGGLGFGYTTRAVLDRLGPDARVTVAELLPVVVTWNRGLLAPLAGAPLEDPRVTVVELDVGKHMARQSGTYDVILLDVDNGPTALTHPDNHGLYGRVGLAHAVQALRPGGVLGVWSAGPSPAFERRMEQAGFTVQVLHPAAHGTKGTRHTLFMGKRRPQGRR
>NZ_CP017172.1|WP_140794228.1|6518267_6520892_+|ATP-dependent-chaperone-ClpB
MRLDKYTVKAQEAIHEGQTLARRADNPQYEPEHLAAALLGQKDGIVDPLLRKIGADVKLFAARLGEALQKLPRMQGGESAMLGQRLLKTFDKAEDEAKSLKDEFISSEHLLLALTHDKGAVGEVMKSSGVTRERVLSGLKDVRGSGRVTSQDAEATYQALEKYGRDLTEAARAGKLDPVIGRDEEIRRCVQVLSRRTKNNPVLIGEPGVGKTAIAEGLARRIVDGDVPEGLKNKRLVSLDLGAMVAGAKYRGEFEERLKAVLKEIADAAGEVILFIDELHTLVGAGKAEGAMDAGNMLKPALARGELHCIGATTLDEYRKHIEKDAALERRFQPVMVGEPSVHDTISILRGLKERYEVHHGVRIQDNALVAAATLSHRYIADRFLPDKAIDLVDEASSRLRIEIDSMPTELDDVRRKMTQLQIEREGLRKETDPHSQERLGQIEKELANLSEKFNALKVHWDAEKTAIGAIRGLKEKQEKAKNDQAAAERQGDLNRAAELKFGVIPSLDKELKAQNEKLTELQKNQKFLKEEVDAEDIAQVVAKWTGIPVSRLMEGEVQKLVHMEDRLANRVIGQRSAIEAVSNAVRRARSGLQDPNRPIGSFIFLGPTGVGKTETAKALAEFLFDDDSAMVRIDMSEYMEKHSVARLVGAPPGYVGYEEGGQLTEAVRRRPYTVVLFDEIEKAHHDVFNVLLQILDEGRLTDSQGRTVDFKNTVLILTSNIGSQDIQAGMAGKEELDERTRNEVMDALRAHFRPEFLNRVDEVVIFEPLRKKDIYRIVDLQLARLSKLLADKRLTLELTEKARELLAERGYDPTYGARPLKRAVQKNLLDPLALKVLGGEFVPGDHIQADAGPDGLTFAKVLVDTSKNVKRSA
>NZ_CP017172.1|WP_174259070.1|6517504_6517999_-|hypothetical-protein
MGATGLKVSVNRRRKVVRLAYVAPFTEGRQGAHWYAAHHALPRLLSRATNAAVQAYVYDPDEGEQVIAYGNGRRVGGERVVYEDVELPVPLDQMDDAAFKHMQERWPVGHLAYVFGLTRKELLRLPRVAPGHELELEGRDAEGAAVLEALLPTCQVTLPESDAL
>NZ_CP017172.1|WP_140794227.1|6516856_6517498_+|hypothetical-protein
MKHSGRKGLPGGIRFAAIVGLVLSILTGWAALMEAVEMANFYEARSLRMEQELPRIPGAPALDPKIFEVYYAALEPMREPRAVLLGLLAVACAFVSVSAARMLSPENLPRDAMRRVLSRAAIIAAGLRTIDGAQMSVAKQRLFAALAEPMSKMPEFPPDITVEASREILSAMGTGSAIFGTVVVAGTFALLGQYFRSQGVREAMAVQDGPQEE
>NZ_CP017172.1|WP_140794226.1|6516545_6516860_+|DUF1844-domain-containing-protein
MSSGDEKRGETFVMRGEARSASEESISFSTFIVGLGTAVLIHLGGAPNPETGQTAKDLPLARQNLDLLSMLRAKTRGNLTAEEEKLFDGLLADLRLRYVEATKR
>NZ_CP017172.1|WP_140876483.1|6516168_6516549_+|RNA-polymerase-subunit-sigma
MADSADPKYLDKRTVERYVRSGQLDEVEYERHLQGLPDVAEKSVPVETLMLDDADDFDDEEDDFDDEDEDDDDDTSDDEAETSAAAESTDGDAAEAGEDDEDEDEGDDDAATASNETPDDEGPVSA
>NZ_CP017172.1|WP_140876481.1|6515419_6516076_-|thiamine-phosphate-synthase
MNAPSRPYLPRGPYLLCDDSVLPEISLVDKAARLVAGGARVVQLRMKRTPVRDALAATRQVVALCRREGALCLVNDRVDVALLADADGVHVGDEDVPAEDARALLGPGRLVGVTVRDVVGARAAQAAGADYVGLGPIFPTSTKQVPAPVLGLEAFAAVVRDSPLPVVGIGGVGLANIASVAAAGAYCAAVVSDALLAADITERVRQLADAFEQGRFGA
>NZ_CP017172.1|WP_140876479.1|6514634_6515399_-|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein
MNTHSRHHGPAPRRPNIGITPDWSPAGEQPFARYELKVPYADAVLRAGGLPFVLPYSDEPACVESYLDRISGVLVTGGAFDIPPSAYGEDAREGLGALKEGRTSFEAALMRGALKRNMPVLGICGGMQLLNVILGGTLYQDIGREVEGAREHEQKHDRTHPQHPVDVKSGTLLAEAVGHGQLMVNSTHHQSVRGVGNDVTITAVAPDGVVEAIESSVHTFAVGVQWHPEYMSTTIPVHVGLYKAFVQKAREHRR
>NZ_CP017172.1|WP_140876485.1|6526039_6527368_-|DUF418-domain-containing-protein
MSESSPLPASTAPGASPVDASERVILLDALRGFALWGVFVSNSLMWLSGRAFMPREAAAPLEASGLEQVVSGIYQLFVTQKFISIFSFLFGLGFSIQLARAEARGVSAVPLYSRRLLVLLGIGLAHALLLWTGDILHTYAMVGFLLMAFRARANRTVLFWALGLVTVMPFLVPAAIRYAPILLNGAEAAAEAVKASQARDRVLKADTLAALSSESFWTAQVGNARFFLENLGGGFRRVLWMSLILGRFLLGLLAGRLLLLQDVARHRALLRRTLAWGLGVGLALNGSGLVLYRLRKAGVLEWDPQGPWMMLLNSLQEPGYIAMGAAYVAAFALLFQRERWRRWLGVLTPVGRMALTNYLMQSAVSIWIYDGWGLGFIGKLPPSRIVVICCIVFAAQVVLSHLWLSRFRFGPAEWLWRSLTYGKAQLMRRPAGDGDAPGVAAS
>NZ_CP017172.1|WP_140876487.1|6527508_6528819_+|amidohydrolase
MKVSHLLPLLISLAVPGGLALAAETPPVLGGLDALYPELDALYRDLHQTPELSNQEAKTAAKLADRLRKLGFEVTSKVGGHGVVALLRNGQGPTVMLRADMDALPVEEKTGLPYASKQKAKDAAGATNPVMHACGHDVHMTSLLGTATLLARSKDRWRGTLLLVGQPAEEVGAGARQMLQDGLFKRFPKPDFAVALHVNTAAAGTVEFTPGYAMASVDGVEITLHGKGGHGAYPHTTVDPVVMAARVVLSLQTLVSREKNPLEPAVVTVGAIHGGTKHNIIPDDVKLHLTVRSYKPEVRKALLDGIERIAKAEAMASGAPRPPDIAITEGTPSTFNDPALTRRLVGAVSRVLGEKNLQEAPPVMGGEDFSEYGRAGVPAVMLWLGSTEPRQYAQAKAAGTALPSMHSPLFAPDRERTLRTGVTTLTTAALELLDKP
>NZ_CP017172.1|WP_140876489.1|6528950_6531170_+|putative-Ig-domain-containing-protein
MSPLLNRNHSLRALLGASLWWVASGFQSEAIVSHEGTVRSGTSVSLSLQVSSGPSQTFTRTGQLVACIALPGGWQAPGGSYTHAGSAATAAQPGAPELSAEAQSAWPVNGATWHCLVSENVTTTNQEVQSTAQLTLPVPAAAQGAYRVRYQSGFREMTPPVGGGQAPTYQPTDFSGRLERLLHVNVAPATTFDDWQAGVATGILVTPSVTRAWHGNGTFLAAATGNTELLRSSDGRQWTGFVPVSEGTTSPLPLERLVYSQRKWFGVSNGRIVVSSDNAHTWAPAYQDPAPGGRRFLELALSGNRMVAVGTAGLIASSTDGQRWTDESINGAYDVVTLVPGQSSFLAVANPMAGAPSQLPVLVRPQGAGAAWEVFQPATLAGLTIAQLTAGNGRFLAFARPNQVPPPPPLAAEPTSGFFLSEDLGSTWTRVESLQLPADAPSPTPLMTFVDQSFVVSWTAVDPQLVEVLPPFELQVSADGKEWTAHPTGAGGNYASTAFASGETSVVAVSQRRLLVATRRPWPLPELLTETLPPFRLGTAANVVLSTRGSGTLTFELEGTLPSGLTFTPTTGTFTGTPAQSGSTAVTVRVRDARGGVAARTYSVDVVGTMSISSDALASATQGTAYEARFTVQGGRAPYTWSLGGGTVPGGLTLQQRDGAYVLSGIPTASGTFPLTVRVTDSANQTAARSVSLQIAPTPPPVEDKGDAPSGCGCNGGGAGVQALGLAALALIGRARRKR
>NZ_CP017172.1|WP_140794236.1|6531226_6531643_-|winged-helix-turn-helix-transcriptional-regulator
MSANKRPGPLARKMAKLAVERGNLYVPSCPSRGVLDHVTSRWGVLVLIALLEGTRRFSELRRRVAGVSEKMLSQTLQALEQDGFVLREVHPVIPPHVDYSLTPLGEEVATRVEALADWIEDSMPRIAAARAVYTPKKG
>NZ_CP017172.1|WP_174258896.1|6531744_6532599_+|SDR-family-oxidoreductase
MILVTAATGKLGRLVVTGLLEKVPAKDIAVAVRDPSKASDLAAKGVQVRQADYSKPETLGPALAGADKVLLISSSEVGQRAVQHQAVVDAAKKAGVRLLAYTSILHADTSGLVLAGEHKATEEAIRASSIPFVFLRNGWYTENYTENLAPALAHGALIGSSGQGRSAAATRADYAAAAVAVLTGTGHENKIYELAGDTAFTAAELAAEVSRQAGTTVVYKDLSQADHAGALIGVGVPAPFAELLADSDAGVARGEMNDSSGDLRRLIGRPTTPLADAVAAAVKR
>NZ_CP017172.1|WP_140856162.1|6532647_6533199_-|RNA-polymerase
MSELTELLDHARKGEQGARDALMAAAYQELRDMAQRAMSDVVSTPSLQPAVLVKEAWLRLFGAGAPVEARRHFFSAAAQAMRRVMVDRTRLRRAQVREARLERVSLGDVEADVPAGLSMEVLELDRALSELDTFQPRLARMLELRYFVGLDLLDTAAVLGVSPVTVKRDWAYVREWLLTRLGN
>NZ_CP017172.1|WP_140876491.1|6533508_6534318_+|hypothetical-protein
MKPLLSALLPLLCLASAASAAPQAPVAVRSDLTFLSGPPTLTFAADWGVTLSGQPEAGGALDIVYDTSRLPLCRGTGWTITGFAMSNRGPVQSFPVADATTVGAIAQTQLALAQGGTLELWFQNTDTTGCSNWDSNLQYNFHTWVTQNPTISFHPAPAWTYTVHGTLQGGTTLMVDYDIGRIAQCRAQYLNYKAWGTTAYYRVNGGPVTMLSLTASWGEWDAQFWRQIPAFIPLPPGPATLELWFSTQDRKGCQQWDSRHGQNYVFAIQ
>NZ_CP017172.1|WP_140794240.1|6534469_6534904_-|arginine-repressor
MVVGMNLDEAILRLIAEREIGDQAVLQQLLEAEGQAPSQSTLSRRLKKLGILKVGGRYQRMPATPAVMPERPRVTILEAPPNLLVIRTAPGFAPVLALALDKERELPGLAGTVAGDDTIFVAVTDPALLRDVRAAVERLLSLGA
>NZ_CP017172.1|WP_140876493.1|6535073_6536081_+|N-acetylornithine-carbamoyltransferase
MKHVTHIKDLGPEGVEAVLAQAAAWKQKGPEHALFANTLLGMVFFNPSLRTRTSFEAVMLRGGGNAIILDVGAGVWKLEHREGAVMNADRAEHLKEAAPVLSRFVDMLGVRTFSQGGGDEEDELDPVINAFRKWSTVPVVSMESAREHPCQGLADMLTLRETFGSTKKLPVTLTWAPHIKPLPKAVPNSFLLSAAAAGCEIRVAHPPGFDLHPAVRAEAEAYAKATGGSVTYTHDQDEALAGSRAVYAKSWGPTAAAAFSPNDVTALLASYSGWMPTRLTMSRAQKDAAFLHCLPVRRNVEVADEVLDHPNSRVVDEAGNRYHVQRALLHWMRSR
>NZ_CP017172.1|WP_140794242.1|6536124_6537051_+|acetylglutamate-kinase
MPLSPDPYSALRNAAKYVQQFRRKTFVVKLGGAMLSDPRLRRAACEQIALLWTFSIRPVVVHGGGPELDTLCDALHLPVEKVAGRRVTSAPVLDAAKMVLAGKLHTDLLADLQAAGVPAVGLSGVDAGLIKARKRPPVMVTEAGATEGKLVDYGLVGDIEQVDTRVVEHLRSADYVPVIAPLSGGTDGAVYNTNADTVAAALAVALSAEKLFFLVQVPGLLKNVSDPSSLVTLANLTDLATMESTGAIAGGMKPKAHAIRHALVGGVGSVHLVSGVQPNALLEEVFTNEGSGTMVVRENAQKPAGAVG

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_13

6844968-6845053

Orphan

Consensus_repeat	Method
TCGTCGAGCGGCGGCGGAGGGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_13

>merge|NZ_CP017172|13|6844968-6845053|CRISPRCasFinder
TCTTCGTCGAGCGGCGGCGGAGGGGGCATGCCCCGCGCATCCGCGCTCTCGACAGGTGCATCCACGTCGTCGAGCGGCGGCGGAGG

>NZ_CP017172|13|12|6844968-6845053|CRISPRCasFinder
TCTTCGTCGAGCGGCGGCGGAGG	GGGCATGCCCCGCGCATCCGCGCTCTCGACAGGTGCATCC
ACGTCGTCGAGCGGCGGCGGAGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140794443.1\|6842980_6843478_+\|histidine-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|224973
NZ_CP017172.1\|WP_140794449.1\|6847907_6848885_-\|30S-ribosomal-protein-S2	unknown	unknown	gnl\|CDD\|235396
NZ_CP017172.1\|WP_140794454.1\|6856364_6858101_-\|DNA-repair-protein-RecN	unknown	unknown	gnl\|CDD\|223571
NZ_CP017172.1\|WP_140794452.1\|6853502_6854207_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|128563
NZ_CP017172.1\|WP_140794444.1\|6843491_6843824_+\|iron-donor-protein-CyaY	unknown	unknown	gnl\|CDD\|274572
NZ_CP017172.1\|WP_140878485.1\|6833097_6834183_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340838
NZ_CP017172.1\|WP_140794447.1\|6846125_6846878_-\|UMP-kinase	unknown	unknown	gnl\|CDD\|234735
NZ_CP017172.1\|WP_140799529.1\|6842125_6842791_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140876689.1\|6852437_6853460_+\|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	unknown	unknown	gnl\|CDD\|236971
NZ_CP017172.1\|WP_140794450.1\|6849264_6852087_-\|preprotein-translocase-subunit-SecA	unknown	unknown	gnl\|CDD\|237259
NZ_CP017172.1\|WP_011555314.1\|6855506_6856304_-\|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP017172.1\|WP_140794448.1\|6847094_6847748_-\|translation-elongation-factor-Ts	unknown	unknown	gnl\|CDD\|183447
NZ_CP017172.1\|WP_140876685.1\|6838323_6842103_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235832
NZ_CP017172.1\|WP_140876683.1\|6836467_6837190_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237030
NZ_CP017172.1\|WP_140794446.1\|6845529_6846087_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP017172.1\|WP_140794438.1\|6832534_6833089_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237865
NZ_CP017172.1\|WP_140794453.1\|6854369_6855287_-\|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl\|CDD\|366703
NZ_CP017172.1\|WP_140796619.1\|6837342_6838164_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133031
NZ_CP017172.1\|WP_140794437.1\|6832009_6832531_+\|DUF1768-domain-containing-protein	unknown	unknown	gnl\|CDD\|378035
NZ_CP017172.1\|WP_140876681.1\|6834230_6836471_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340831

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140794443.1\|6842980_6843478_+\|histidine-phosphatase-family-protein	gnl\|CDD\|224973	COG2062, SixA, Phosphohistidine phosphatase SixA [Signal transduction mechanisms].	1.01793e-20
NZ_CP017172.1\|WP_140794449.1\|6847907_6848885_-\|30S-ribosomal-protein-S2	gnl\|CDD\|235396	PRK05299, rpsB, 30S ribosomal protein S2; Provisional.	6.88098e-165
NZ_CP017172.1\|WP_140794452.1\|6853502_6854207_+\|diguanylate-cyclase	gnl\|CDD\|128563	smart00267, GGDEF, diguanylate cyclase. Diguanylate cyclase, present in a variety of bacteria.	5.0794e-05
NZ_CP017172.1\|WP_140794444.1\|6843491_6843824_+\|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_CP017172.1\|WP_140878485.1\|6833097_6834183_-\|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.	2.27471e-98
NZ_CP017172.1\|WP_140794447.1\|6846125_6846878_-\|UMP-kinase	gnl\|CDD\|234735	PRK00358, pyrH, uridylate kinase; Provisional.	7.49448e-150
NZ_CP017172.1\|WP_140796619.1\|6837342_6838164_+\|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_CP017172.1\|WP_140794454.1\|6856364_6858101_-\|DNA-repair-protein-RecN	gnl\|CDD\|223571	COG0497, RecN, ATPase involved in DNA repair [DNA replication, recombination, and repair].	0
NZ_CP017172.1\|WP_140794450.1\|6849264_6852087_-\|preprotein-translocase-subunit-SecA	gnl\|CDD\|237259	PRK12904, PRK12904, preprotein translocase subunit SecA; Reviewed.	0
NZ_CP017172.1\|WP_011555314.1\|6855506_6856304_-\|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	5.5045e-78
NZ_CP017172.1\|WP_140794448.1\|6847094_6847748_-\|translation-elongation-factor-Ts	gnl\|CDD\|183447	PRK12332, tsf, elongation factor Ts; Reviewed.	1.11675e-104
NZ_CP017172.1\|WP_140876685.1\|6838323_6842103_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|235832	PRK06567, PRK06567, putative bifunctional glutamate synthase subunit beta/2-polyprenylphenol hydroxylase; Validated.	3.05386e-177
NZ_CP017172.1\|WP_140876683.1\|6836467_6837190_+\|hypothetical-protein	gnl\|CDD\|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.8957e-05
NZ_CP017172.1\|WP_140794446.1\|6845529_6846087_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	3.60497e-96
NZ_CP017172.1\|WP_140794438.1\|6832534_6833089_-\|hypothetical-protein	gnl\|CDD\|237865	PRK14951, PRK14951, DNA polymerase III subunits gamma and tau; Provisional.	0.000284644
NZ_CP017172.1\|WP_140794453.1\|6854369_6855287_-\|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_CP017172.1\|WP_140876689.1\|6852437_6853460_+\|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	gnl\|CDD\|236971	PRK11760, PRK11760, putative 23S rRNA C2498 ribose 2'-O-ribose methyltransferase; Provisional.	5.64151e-44
NZ_CP017172.1\|WP_140794437.1\|6832009_6832531_+\|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_CP017172.1\|WP_140876681.1\|6834230_6836471_+\|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.	3.71655e-31

>NZ_CP017172.1|WP_140794444.1|6843491_6843824_+|iron-donor-protein-CyaY
MMDEARYNQLVSAAFKRILAAADAIDPDILEADSTGDMVTLTAASREKCIVNTQRAVRQIWVAGRGQGIHFDYDAATGTWKDDKGRGLELMSFVADVVRGITGADFAYPG
>NZ_CP017172.1|WP_140794443.1|6842980_6843478_+|histidine-phosphatase-family-protein
MRLFLVRHADADAEIPEGLGDEARALTAKSRTSTAHHFASLTERIGPVGRILTSPLVRTVQTAQILSISAKFEGPLKVHRCLLPDMPVGAVEPVLNEYADENLVLVGHQPSMGALAAHLLGMQSFPKPVNPGTVIGLERAEGESSPPFKFLFYAAPGQQVLDIIQ
>NZ_CP017172.1|WP_140799529.1|6842125_6842791_-|hypothetical-protein
MRKVLWGLWVLVAFSACKKPEDASAPPAGAVGEQAPGAPAGVVEAGPYTVTKEKLDAYVGYQRRMLDVYGSLMKGLQNLGALVDAGTPEAMAAAREGLKVVEAKAKAEAEARREAQLSEADVNGIAEVVTAVISQRQLGRTLQYDEELKKLESLQAKLPPEQQQGMAPQVASMRAQVEAFQTLADARRDYGDANVDVVLTREEDLIQNYQEMIRVFTGTRR
>NZ_CP017172.1|WP_140876685.1|6838323_6842103_+|FAD-dependent-oxidoreductase
MRALTDLPSDPTPPLTLGLPGFVFEDLYRPAGLRRLAERFDAQLAEDEPELFHAFDAYRKSGGKSVSGAAESDLLIRVSRHVSRFVTRLFRVEQELERMAGRLKGELPLFDFKREFITRRVFKKGAADRPALAEFPSLDARMRLMLQLGFPEALATGDLERGLAESVLALMDLERLFSNALPAERQGEAEALRARWSALREVLLSTPEGKDAFGSSLVTQGDDAAELQSVRALLSLADRWTYARALHPETKDIFHAWPTHRIPKPLVFDQLVHLQRPDNELPEATEGLEHHLRHRDGFKLTDRRGTSRDVMNEVDYCVLCHERQKDSCTKGFPAKDPVAEGHHYKKNPLGIPLNGCPLDERISEAHLLKREGNSVAALAMVTLDNPMCPGTGHRICNDCMKACIFQKQEPVNIPLAETATLTDVLNLPWGFEIYGLLTRWNPLNVRRPYALPYVGRNVLVVGLGPAGYTLSHYLLNEGFGVTGIDGLKIEPFPDALVGRNGHALQPIRDWSALTSELDERILEGFGGVSEYGITVRWDKNFLTLIHLTLARRESFRIHGGVRFGGTLTVEDAWALGFDHIAIAAGAGRPTIIGMKNNLIRGIRKASDFLMSLQLTGAFKKDSLANLQVQLPAIVIGGGLTGIDTATELMAYYPVQVEKALARHEKLVSQVGEEAVLARLDAEERATYQTFLEHGRAVREERQKAKALGRDPDFIKLVRAWGGVSLVYRRSLTESPAYRLNHEEVTKALEEGIRFIERMSPVEALPDASGAVRALRFERMVTVDGKLKGSGQFFELPARTVCVAAGTSPNVTYEKEYPGTFQLDARGEYFQSHELVDAEGGFSLVPVKAKEDPAAKTGFFTSYQQDGRFISFYGDNHPTYAGNVVKAMSSAKDGHPQVARLYAKEVAALDFTDEVAQAARDARRAAHFAKLDEAFTATVVAVNRLTPTIVEVVVRAPFAASHFSPGQFYRLQNFERNAPVVDGVRLTMEGLALTGAWVDKEKGLMGTIVLEMGSSSRLCAALKPGEPVVLMGPTGAPTEIGHNETVVLVGGGLGNAVLFSIARSLKAAGCRVVYFAGYRQKSDSFKHDEIEAGTDQIVWSVDTGDTIEPRRPQDSAFRGNVVQAMVAYAEGKLGPAPVVALADVDRIIAIGSDGMMRAVAEARHGVLQPHLKPGHEAIGSINSPMQCMMKEICAQCLQRHVDPVTGKETWVFSCYNQDQRLDQVDFVNLRQRLRGNTVMEKVADVYLAQLFKQAPHLKRV
>NZ_CP017172.1|WP_140796619.1|6837342_6838164_+|glycosyltransferase
MHAPFVSVVIPAYNEGQRLPRFVAELTRVFLERSAPPVEFVVVDDGSAPEQAELQRASVEAAQARLATAGARHQFTYVAAPRNQGKGLAIRLGWRHASAGVTWLAFLDADGAINAEEFHRLVAMSASEMAQNVDVLAGSRILMAGRRVVRSLHRHLQGRIFATLTDANFKLHFYDTQCGVKFVRADILRPLLDVLQEQRWLLDVELLVLLKRQGARFLEVPIDWEDFGGSKVIPGLDAARMFWGLLQLRRRLEHVSLPTHRDALPEGEPHAQR
>NZ_CP017172.1|WP_140876683.1|6836467_6837190_+|hypothetical-protein
MKLLGRDIPARELIARIEERLRTRGLPTSEEVELPPEGVEPRVEPLTFNLHALEEYADATRALPLHTHRGGVGQVVLLAKWAFRKSCQVFINEALGRQRVFNGHVRDSYAQLSAEVLRLRREVEALRSRPVPAVADAAVPQPSTASTTTTAPAIDAVLPKPRDTKAQSRQPVSAASTGKSAVPPPAAHAQAPVPAAGEPVASKTARAKKAAPSAPAQSSAEASPRRNASGQKKRRNKKSR
>NZ_CP017172.1|WP_140876681.1|6834230_6836471_+|glycosyltransferase
MAIHQLIPSFVPGDATGQAALHLQLLLRRMGHAGALYADEVGPGLEGLASPASALRPAPGDLVLYHHGIASPLSSRLMHLPCRRGIVFHNISPARFYEGLPLADALVAGRAQLAAMAPFADVAIGVSDFNAAELRVAGYRNVHTVPLFIEPERFSRASADAKMLQRLEGPGPVLLGVSRVMPHKRFEDLLALHREVLRLRPQARLLMVGGYEPGSRYFRMLQREARGLRGVSFLGRLNHAQLVAAYRSASVFVSMSEHEGFGVPLIEAMAAEVPVLAYAAAAVPETLGGAGVAFDQKRFAFLAELAVDLSEDVSLRKPVIAGQTRRLEHFSAHSVQTGFTKALETVLPRPAPTKPRKAPERPRVALVVQRYGEVTGGAEKLAAQMAEHLAPHWDLTVLTTCAKNHLVWDNAFPPGPDVVDGIKVLRFPSTRVRNIRGFNGLSRQVFDKSNERLREEQWVAEQGPMCPGLLHHLATERDAYDGYLFFTYLYAPTVWGLPLVADRALLVPTTHDEAPVRFGVYRDVFERPRALLCLTPEEHTLIEKYFPNHAPTRVVGVGVDRPRADGARFKEKHGIHRHYLLYIGRQEPGKGVPELLQHHQALKERFEDAPDLVLAGDTNMELSGEGVRYLGRIDEQDKHDALAGALAVVVPSRYESLSLLTLESFAQGTPVLVNGRSDVLVGQVERSGAGRAYTDLESFIQGLREVGAERGPMGKRGLAYVKKQGWPQVVAAYREEMQRILEEKRQ
>NZ_CP017172.1|WP_140878485.1|6833097_6834183_-|glycosyltransferase
MGPIAFDATLWDEPTTGIGLYTRCLASALEALGVQLTRVGARSSGEAPRAKAGRTAWTLGGLPRVLRGSDAPLYHAHGNFNLPLIRVPGMKYVLTVHDLIPLLMPETVSSAFRWQFRLWLSRSLMVADQVVCVSERTRQDLLARYPEAESRTVVVPNGVDHVHAPALDDTSKDFLRALSLPKEYVLYAGSLDVRKNVDLVLDALERLRLRGRPVSLVLAGQSWFGAGRVEARISRLRSEGFEVRSLGYQSDAVFYELMRRAAVFVFPSRYEGFGLPPLEAMRLGTPTIVSTAGSLPEVCGDAALSVGPDDANGLARALDRLLHSPEERRALAERGKAQAAKFTWKRTAEGTLAAYEAALRR
>NZ_CP017172.1|WP_140794438.1|6832534_6833089_-|hypothetical-protein
MRKLVWSGVMLCGLLAGCAGRQDTGTAPVEPPPAEAEASAEVSAPAPEDTQATEIPPAEEGEAKAAVQPLVVTPNPEPKDPINIRSAKVDGGILTVAVMHGGGCAEHTYSLAWDGNLQQGVDGTPVANLVLVHDGNNDRCKALLRASPRFDVSSVSQRFGAQFGKTSGTVNLVLSDQAQVRYDF
>NZ_CP017172.1|WP_140794437.1|6832009_6832531_+|DUF1768-domain-containing-protein
MSEAGQQRFTFFWQAHSPFSQWHRSDFVVDGVHYVCAEQYMMAGKARLFGDTEALASILSSKSPKTHKALGRKVRDFDNARWEKARERIVYEGNRAKFTQSEELLNALLATAGTELVEASPVDRIWGVGLDEEDPRIQHPAKWRGLNLLGKVLTKLREDLMAEGVTKASPAKP
>NZ_CP017172.1|WP_140794446.1|6845529_6846087_-|ribosome-recycling-factor
MSGDVVAELKGRIDKSIEGLRTDLTKVRTGRASIAILDGVRVDYYGTPTPLSGVASVNAPEPRLITIKPWEKSVLKDIEKALREANLGINPMNDGEMIRLPFPPLTEERRKDIAKQVKNKGEEFKVTIRNLRRDANEALKTQLKDKKITEDDHKRITEVVQKQTDAGITQVDEIVKKKEKEVMEV
>NZ_CP017172.1|WP_140794447.1|6846125_6846878_-|UMP-kinase
MSSDTKKPLPYKRILLKLSGEALMGEGKYGIHPPTLMGIAEEVIEVAQAGVEVALVIGGGNIFRGVAGATEGMDRASADYMGMLATCINSMAMQDALEKKGLHTRVLSAIKMEQIAEPYIRRRAVRHLEKGRVVIFAAGTGNPYFTTDTAASLRAMEINAQVILKATKVDGVYSADPKKDPTARRYRSLTYMDVLKQNLNVMDSTAISLCMDNKLPIIVFDLTQRGNIRRAVLGDGDIGTLVGGSETVWA
>NZ_CP017172.1|WP_140794448.1|6847094_6847748_-|translation-elongation-factor-Ts
MAEVSAQMVKELRERTNAGMMDCKKALSESGGDFAKAEEWLRKKGIAKAAGKEGRVASEGVIGTYVHSGRIGVIVEVNCETDFVARNPDFQELVKDVAMQIAAAGPKFVRREEVPTDNLDKEKDIQRELLKQQGKPEAMLEKILVGKMEKYYEGVCLVDQLWVKDDKKKVGEMISERAAKIGEKVSVRRFVRYEVGEGIEKKKDDLAAEVAKTLGQA
>NZ_CP017172.1|WP_140794449.1|6847907_6848885_-|30S-ribosomal-protein-S2
METQDTQTQQQAMAAAGGITMRQLLEAGVHFGHQTKRWNPKMKPFIFGARNGIYIIDLQKTVVMARSAFRFVADITARGGSVLFVGTKKQAQDVVREEAARAGQFFVTSRWLGGTLTNFKTIKQGIDRLKTLEKMAEDGTFERLPKKEVAQLEREREKLEKNLGGVKEMSKLPRCVFVIDPKKEHIAIHEAGRLGIPVIGLVDTNCDPDGIDFVIPGNDDAIRSIKLFTSKIAESCLEGAARYRASGAAERDEQEEREGRDDRGDRRDDRRGPRRGDRRDDRRDRGGDRGGDRRGPLVEMKAAAPVASTEPAAEAAAPEGEAAAE
>NZ_CP017172.1|WP_140794450.1|6849264_6852087_-|preprotein-translocase-subunit-SecA
MIEWTLKKLIGTKNERELKKAHAKVARVNELETRMRALKDEDFVSETNRMRQEIQNGRSLDDLLFEAFAITREAARRVIGQRHYDVQLIGGMFLHEGCIAEMRTGEGKTLTATLPTYLNALSGRGVHVVTVNDYLARRDAEWMGRVYRFLGMTTGCVLHELNDKQRQEAYRSDITYGQNNEFGFDYLRDNMKFRLQDYVQRELNFAIVDEVDSILIDEARTPLIISGPTEDSTDKYYRVDQVIPGLVPDQDYTLDEKHRSVSLTDDGIEKLQKRLGVGNLYDPGEIEMLHHVDQALRAHTLYKRDKDYVVKDGEVVIVDEFTGRQMPGRRWSDGLHQAIEAKEGVKIENENQTLATVSFQNYFRMYSKLAGMTGTADTEAEEFAKIYNLDVRVIPTNRPPIRKDLQDVVYKTEREKFEAVAAEIEELHKAGQPVLVGTVSIAKSEVVASFLKKRGIPHNVLNAKQHQREADIVAQAGRKGAVTISTNMAGRGTDILLGGNAEVLAKASMGPPPEPPTSAPEGQPLDLTAYEAELAAWEQKLADTKTKLEEQTKKEREEVHNAGGLFIIGTERHESRRVDNQLRGRAGRQGDPGGSRFFLSLEDDLMRIFGSERIQGLMERLGMEEGEVIEHVWLSRAIEGAQKRVEGHNFDIRKNLLEYDDVMNQQRRTIYKLRRQVLAAGAGVPLVEYDEDPKTRIKTRSERTVSWADFRELILDSMEDVIVSLTDTYAPTRGVEGWDIAALQQGVKETFNLEMNFEGVGNREELQEHIYKAAEKVFQAREEEFGENFMRFLQYNYLATIDRLWKDHLLAMDHLRQGIGLRGYGQKDPKQEYKKEGYQGFIQMLSAIKAQFVTQLMHVQPRSASSAAEEAARIQRQLAQQQKKAVEGRATADGKLDEGSVAAAARPAAASKPAVGRNDPCPCGSGRKYKKCHGASEASV
>NZ_CP017172.1|WP_140876689.1|6852437_6853460_+|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM
MPARTLAARPGRWLWTCRAGFEAHLFEELEWAGAEPRLLGEALVESDAISGPPPAFARAGYQVAATLTATSPEAVAEAATRTVLALPGRAPWAVQAFTPDTPRGNALAPVAEALESAVSARLPPGRRVEDAQRAREAGALLVSLCVAPDDVTVVGAVHAREAVSLAAGGRRRMRRAGDAPSRAAMKLEEALDGLAFEPGRGDVCVDLGAAPGGWTQRLVSRGAKVVAVDPARLMPELTGNPRVKHVQESAFAYAPDEPADWLFCDMAWRPLEVAQLLAKWGRRGWAQHLVANIKLPMKDKNPILLRVRHTLVQEGGWEGLTVRQLYHDRDEVTVTAHKMK
>NZ_CP017172.1|WP_140794452.1|6853502_6854207_+|diguanylate-cyclase
MPYPLDDATATALIALHPWVLTRSPQAPVQAAVEVLVQAEQARRGQPDAKTGALQVPALTQGNLLKEEYDLSTHGHHDGWRVGAVIADVQGMINVNARFGFPTGDAVLRATVESLSAQYPGAKVVRIHADAFAALLVPTSQLTVEEHLAVPTRERLAQDVRRVLPQGTPDADVPSWTVSLLELTVDAPSHWQVLGPLLWAELERTHVMERTGRAQGLQRRRIRLDGSIPGPATL
>NZ_CP017172.1|WP_140794453.1|6854369_6855287_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MAKKSFTLMVIPDHDAPVKRYTIQRSFLTQVGMGLMLVVGLGVGASVHYFQVAADASENRILREENLTLRSQLKSVRERIEHIGSTLDRVERFDQKLRAVTLLSDPQRNLAMGPTEPEAGTSAPATDTQFTQLTSTETPKALMGRLDRLSAEATRQEQSLQELQAYFQDQKSLLASTPSIWPARGWVTSDFGSRLDPYTADRVMHGGMDIAAPHGKEVFAPSDGTVVFAGLEGGYGNVLVIDHGYGIKTRYGHLSKMLVKAGDRVKRGMHIAAVGNTGRSTGPHLHYEVRVNGIGQNPRKFILEE
>NZ_CP017172.1|WP_011555314.1|6855506_6856304_-|Stp1/IreP-family-PP2C-type-Ser/Thr-phosphatase
MSSTAGQTAASRLKIISAGLTDVGRKRNHNEDSFLIDDELQLYVVADGMGGHAGGGTASRIAVETIDKEMRRAREGKDNPFLSVPNLQDSPIPEALRTAVERACLAIFTAAQEDARLSGMGTTVISLVVRDEHAFFAHVGDSRAYLIRGDLIQQISEDHSLVNEQIKAGMITPEEAKHSRYKNIITRSVGFEEEVQVDVMGLVSEPGDVFLLCSDGLANMMEDREIHETVVKARTFEEVPKRLIDFANERGGDDNITVIVVRVEA
>NZ_CP017172.1|WP_140794454.1|6856364_6858101_-|DNA-repair-protein-RecN
MLLGLRISNVAVIEEVEVAFGAGLTVLTGETGAGKSILVDALGLLLGGRADADVIRAGCEEASVEGVFARTPALESRLEELGLPDLGEEVLVRRVLGRTGRGKAYVNGSLVTVGVLGRLTRGAVDIAGQHEHVSLFDSGLHRVLLDRYGNLEEVLAAFFREYTGLREVDARMEALGGDEAKVRERAEFLRFQLDEITRLDPEAGEDARLDAERKRLGGAEKLKRHASEAELLVSGEEQSAVETVGRALGLVHESVKCDATLAPVAQALSTALSELEEAQRRLNRYVEGLESDPSRLADVEERLDALKRLCRKHGTHLDGLLKKQGEIEVELGTLENRKEILEELAADRRKVEERARKAATALTRARTASAVTFAAQVREGLGQLAMGKAAFEVRVTPSESLRPDGADDVEFFFSANPGEPPRALAKVASGGEASRLLLALKKALADSDGGGCYILDEADAGVSGAIADVVGRMIKDVSSHRQVLCITHLPQVAAYADAHLLIRKGLKGERTVSEVVVLEAGAERTRELARMMSGVEVTREALGAAEALVRSANRALGTRARRESGPEGSPRGRLRRTA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_14

7201971-7202311

Orphan

Consensus_repeat	Method
CGCCACCGTCGGCACCGCCGTCC	CRISPRCasFinder

6 spacers

WYL

The CRISPR arrays of NZ_CP017172_14

>merge|NZ_CP017172|14|7201971-7202311|CRISPRCasFinder
TGCCGCCGTCGCTGCCACCGTCCTGGGGCTCGCCCTCTCCGTCGTCCTGTCCACCATCCGCGCCGCCGTCCGCGCCCCCGTCCCCCTTGTCCGGTGGGCCCTGGTCGCCGCCGTCCGCGCCTCCGTCGGAGCCGCCGTCGCTGCCACCATCACCGTCGCCACCGTCGGCACCGCCGTCCATGCCGCCATCGCTGGCGCCGCCATCCGCGCCTCCGTCGGCACCGCCGTCCGAGCCACCATCGGTGCCACCGTCCTGGGGCGTGCCGCCGTCGCCCTTCGTGCCGCCGTCCTCGCCGGCATCCGGGCGCCCACCATCACTGCCGCCGTCGTTGCCACCGTCC

>NZ_CP017172|14|13|7201971-7202311|CRISPRCasFinder
TGCCGCCGTCGCTGCCACCGTCC	TGGGGCTCGCCCTCTCCGTCGTCCT
GTCCACCATCCGCGCCGCCGTCC	GCGCCCCCGTCCCCCTTGTCCGGTGGGCCCTGGT
CGCCGCCGTCCGCGCCTCCGTCG	GAGCCGCCGTCGCTGCCAC
CATCACCGTCGCCACCGTCGGCA	CCGCCGTCCATGCCGCCATCGCTGG
CGCCGCCATCCGCGCCTCCGTCG	GCACCGCCGTCCGAGCCACCATCGGTGCCACCGTCCTGGGGCGTGCCGC
CGTCGCCCTTCGTGCCGCCGTCC	TCGCCGGCATCCGGGCGCCCACCATCAC
TGCCGCCGTCGTTGCCACCGTCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_026113776.1\|7210445_7210793_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140876879.1\|7202798_7203860_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238744
NZ_CP017172.1\|WP_140876881.1\|7207924_7208815_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|366166
NZ_CP017172.1\|WP_140878505.1\|7197843_7198719_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140794677.1\|7196088_7196556_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794682.1\|7199918_7201808_-\|BatD-family-protein	unknown	unknown	gnl\|CDD\|379280
NZ_CP017172.1\|WP_140799653.1\|7210866_7211253_-\|thioredoxin	unknown	unknown	gnl\|CDD\|239245
NZ_CP017172.1\|WP_174258925.1\|7196780_7197107_+\|PilZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|377796
NZ_CP017172.1\|WP_140799652.1\|7209736_7210147_-\|DUF1761-family-protein	unknown	unknown	gnl\|CDD\|369962
NZ_CP017172.1\|WP_140794681.1\|7199211_7199922_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140794686.1\|7205827_7206709_-\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP017172.1\|WP_140794689.1\|7209034_7209724_-\|HTH-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl\|CDD\|225253
NZ_CP017172.1\|WP_140794684.1\|7203856_7204867_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238744
NZ_CP017172.1\|WP_140794680.1\|7198737_7199127_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|132912
NZ_CP017172.1\|WP_140856604.1\|7204841_7205831_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794679.1\|7197119_7197527_-\|response-regulator	unknown	unknown	gnl\|CDD\|381100
NZ_CP017172.1\|WP_140794687.1\|7206739_7207729_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP017172.1\|WP_140876875.1\|7194274_7194772_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140876877.1\|7194773_7195577_-\|flagellar-M-ring-protein-FliF	unknown	unknown	gnl\|CDD\|227015
NZ_CP017172.1\|WP_140794676.1\|7195587_7196073_-\|ATP-dependent-helicase-HrpB	unknown	unknown	gnl\|CDD\|374927

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140876879.1\|7202798_7203860_-\|VWA-domain-containing-protein	gnl\|CDD\|238744	cd01467, vWA_BatA_type, VWA BatA type: 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. Members of this subgroup are bacterial in origin. They are typified by the presence of a MIDAS motif.	5.61794e-39
NZ_CP017172.1\|WP_140876881.1\|7207924_7208815_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	5.24518e-25
NZ_CP017172.1\|WP_140878505.1\|7197843_7198719_+\|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.	8.98428e-11
NZ_CP017172.1\|WP_140794682.1\|7199918_7201808_-\|BatD-family-protein	gnl\|CDD\|379280	pfam13584, BatD, Oxygen tolerance. This family of proteins carries up to three membrane spanning regions and is involved in tolerance to oxygen in in Bacteroides spp.	7.33559e-136
NZ_CP017172.1\|WP_140794686.1\|7205827_7206709_-\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	9.51797e-35
NZ_CP017172.1\|WP_140799653.1\|7210866_7211253_-\|thioredoxin	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	4.44665e-34
NZ_CP017172.1\|WP_174258925.1\|7196780_7197107_+\|PilZ-domain-containing-protein	gnl\|CDD\|377796	pfam07238, PilZ, PilZ domain. PilZ is a c-di-GMP binding domain which is found C terminal to pfam07317. Proteins which contain PilZ are known to interact with the flagellar switch-complex proteins FliG and FliM. This interaction results in a reduction of torque generation and induces CCW motor bias. This domain forms a beta barrel structure.	7.70278e-08
NZ_CP017172.1\|WP_140799652.1\|7209736_7210147_-\|DUF1761-family-protein	gnl\|CDD\|369962	pfam08570, DUF1761, Protein of unknown function (DUF1761). Family of conserved fungal and bacterial membrane proteins with unknown function.	2.41761e-07
NZ_CP017172.1\|WP_140794681.1\|7199211_7199922_-\|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.	4.09832e-05
NZ_CP017172.1\|WP_140794689.1\|7209034_7209724_-\|HTH-domain-containing-protein	gnl\|CDD\|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	1.07754e-51
NZ_CP017172.1\|WP_140794684.1\|7203856_7204867_-\|VWA-domain-containing-protein	gnl\|CDD\|238744	cd01467, vWA_BatA_type, VWA BatA type: 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. Members of this subgroup are bacterial in origin. They are typified by the presence of a MIDAS motif.	2.01581e-69
NZ_CP017172.1\|WP_140794680.1\|7198737_7199127_-\|hypothetical-protein	gnl\|CDD\|132912	cd07041, STAS_RsbR_RsbS_like, Sulphate Transporter and Anti-Sigma factor antagonist domain of the "stressosome" complex proteins RsbS and RsbR, regulators of the bacterial stress activated alternative sigma factor sigma-B by phosphorylation. The STAS (Sulphate Transporter and Anti-Sigma factor antagonist) domain of proteins related to RsbS and RsbR which are part of the "stressosome" complex that plays an important role in the regulation of the bacterial stress activated alternative sigma factor sigma-B. During stress conditions RsbS and RsbR are phosphorylated which leads to the release of RsbT, an activator of of the RsbU phosphatase, which in turn activates RsbV which leads to the release and activation of sigma factor B. RsbS is a single domain protein (STAS domain), while RsbR-like proteins have a well-conserved C-terminal STATS domain and a variable N-terminal domain. The STAS domain is also found in the C- terminal region of sulphate transporters and anti-anti-sigma factors.	0.00200594
NZ_CP017172.1\|WP_140794679.1\|7197119_7197527_-\|response-regulator	gnl\|CDD\|381100	cd17548, REC_DivK-like, phosphoacceptor receiver (REC) domain of DivK and similar proteins. Caulobacter crescentus DivK is an essential response regulator that is involved in the complex phosphorelay pathways controlling both cell division and motility. It localizes cell cycle regulators to specific poles of the cell during division. DivK contains a stand-alone REC domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.32661e-31
NZ_CP017172.1\|WP_140794687.1\|7206739_7207729_-\|AAA-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.12179e-93
NZ_CP017172.1\|WP_140876877.1\|7194773_7195577_-\|flagellar-M-ring-protein-FliF	gnl\|CDD\|227015	COG4669, EscJ, Type III secretory pathway, lipoprotein EscJ [Intracellular trafficking and secretion].	1.45053e-33
NZ_CP017172.1\|WP_140794676.1\|7195587_7196073_-\|ATP-dependent-helicase-HrpB	gnl\|CDD\|374927	pfam17001, T3SS_basalb_I, Type III secretion basal body protein I, YscI, HrpB, PscI. T3SS_basalb_I represents a family of Gram-negative type III secretion basal body proteins I. It is the inner rod protein of the secreted needle. YscI is suggested to form a rod that allows substrate passage across the inner membrane of the needle protein YscF through it.	0.00615716

>NZ_CP017172.1|WP_140794682.1|7199918_7201808_-|BatD-family-protein
MRRTGSALGVVFAVFALLASAPAWAASDDLDFYQTADREEVGTEDTFRLTVVVVDAPANAQVKLPESGDFSILSSSRSSQRSISLSGGGPAVIQDVTRHVLVMQATRAGRLKIPPSQITVRGKTYRTQPVELTVKAGRVGGAPPSGQAGRGSGRQPDPFSSIQSQMQQMEEAFGDMMEPDRPTIPRGDSDLFLRASLDRDNVYVGEQVTLSLYIYSRVDLSSVDAVTMPKLEGFWTEEVESPTQLSGEQRVVDGIPYRAYLLRRRAIFPVKSGTLSITPAEADITTGFLFAGHRVHRVSNALKVKVKPLPPGGPEDMPNAHVGNWKLSMDVSQTRVELGQPVTVKVSLEGVGNVKNVTPPALKGPAALKIYDPTTTDKVSPQRHRVQGRRVMEYLVMPQRTGSFTLPALEFTYFDPRARKYEVARTDPVTITVEAGAGGASSIASASPQSSSDQANEQKNVLTAGGLRPVRYQAQFEAPGVPVWKRGFFVPTVLAPLGLLLGVTLMGGVRGRLALRSEAGRGRQQAKAARKRLADAEKLQSSGDVGAFYGEVEKALHGFLEARLGMPVVGLTREVLAEKLTAAGANEERRAKVLFVLEACDFGRYGGGGDPAERQKVMDAAAAAMEGWA
>NZ_CP017172.1|WP_140794681.1|7199211_7199922_-|tetratricopeptide-repeat-protein
MSGYYTPEEAQDIFLKANEAYAREDYAAAKEGYEKLLANGQGGPDVLYNLGTTHLAQGDLGRAVLSLEQARKEGGQAPDLEANLAVARARQVDKVVGATAEDAFLPRVAAATDGPVVAWTFLGTWVAAFVLVLLWRLLGRGRRTAVGVLAVLLFAVAVPSGLLVATHAYVGATVHEAVVLAPTLVARELPQPGARSIFEVHAGLKVRLLEETGRFVRIRLPNGLEGWAEREGVAEI
>NZ_CP017172.1|WP_140794680.1|7198737_7199127_-|hypothetical-protein
MPGGRGPVFSVEALVGKNRLVIRLWGVVTEEEALQIGDASLRALERLRPGFDILSDLTGVTELPESGSGQIERVVEAARVRGFRRVVRVVGRSALAAVRFQRSSRNVGHEAYLAFSLEEAEQLLEGGWT
>NZ_CP017172.1|WP_140878505.1|7197843_7198719_+|tetratricopeptide-repeat-protein
MLLDPQQASGEYVITEPTIVRALLSPPQRTRTMELPRPPPQHPTPHDLATARFTVPMDAHTVPHLRAGLDIALQPLHPFEAHIASFIDGDHAVPELAQAARLPEIEVKVVLKALLERGVVELHRLPGAPAMRTMTDELPILDGQDFLEPEPMALGDEEPPTRQVPPSPPIIPPRTVRRLGIEPGSAEDFLQCAVRLEREGQVDRAIDVLTRAIARVPEAAVLYSKLALILVHQRKDYRRAVELLKRAVALEPNHPVFQQNLLKVTDLAAASPSPHKEEKRGLFARLTGRRS
>NZ_CP017172.1|WP_140794679.1|7197119_7197527_-|response-regulator
MAGNSQAPFHILLVEDEPVIRELVRSMLSDGTVDVVCAATGLEGLKLAKSQTFHLILMDVVLPQLDGISVCRILKGDPATAGVPLYMLTAKAKRSDMESATQAGADGYIHKPFRGAELMALVERLREAGPKPELP
>NZ_CP017172.1|WP_174258925.1|7196780_7197107_+|PilZ-domain-containing-protein
MRTTDGGPQIAERFHPRVDANLPVKVLLKGRSVMVRARDVSMAGLFLMAHPADTARELAIAVPLPGDREIVTTCQIRRREVDGVALEFGELDWDDLIALARYLHPRLP
>NZ_CP017172.1|WP_140794677.1|7196088_7196556_-|hypothetical-protein
MSNDSRIPTLTITHTVPRQTPQNDFGTVLARAANEVVRSGAGLVGGMIPGGPIVSAAVSSAKTVVSAVAPKTMGAGMPATAETGGAAGAGAAAGNQEAWDLLEAQKVLAAEGQKFNMAYLQLQNEMQKESREHTAVSNIMKVRHDSAKAAINNIR
>NZ_CP017172.1|WP_140794676.1|7195587_7196073_-|ATP-dependent-helicase-HrpB
MAMDTLGPVGGAGASPAVEPSRERFSKVLDEVKGPAKGTGVPVATEGPPKPAPTAAPRGVSRAEGVGPAAPGCADVKPGTRVDSVQAARAQQAAQVLDRVGQAQKRLDHILQLAQSGRSFTPAELLALQAHVYRASQELDLAGKVVEKATGGVKQVLQTQV
>NZ_CP017172.1|WP_140876877.1|7194773_7195577_-|flagellar-M-ring-protein-FliF
MLLLFRRAFFLALLVSVTACRERIQHGLDERQANELQSVLVERGLDARKVSEAGKKPTWSIEVADEHASDAVRILSELGLPRLKEEVGCDVFGGGGLVRTPVEESVCRVRVMERSLEKTLQSVEGVLLARVHLVVPSPPRVGQAPGPSKASAMLRVAPGNAARVRQSSETLKVLLAGGVEGLSPEAVSLLVDEVSTRVEAPTVVGVSPLTRLRALLAVLSLMVTGLSVALVLVTLRMRHYRDRTPTPSAPPGPARPVLSPGPARKVA
>NZ_CP017172.1|WP_140876875.1|7194274_7194772_-|hypothetical-protein
MSMESERMDATRVGRKPRPGRSPASVRAAAPTEEVPRLVGPLPFPLERLALVAWVLGRERAGTLLGELGEESAVRAREHLQRLSALPSAQRQAKVAVEFGERADAAARLRRLMSDAPPMLRREIFRRLPPYHRTLFPDGSLAHQASEVPPALGALAERLIREATR
>NZ_CP017172.1|WP_140876879.1|7202798_7203860_-|VWA-domain-containing-protein
MTPVEPWRFTVLGYQAGLAQPLFLLFLLAGMTLGLLALVGALRRRSRVRALLHERHAERFTPGVSVWRPATQGGLYGLGLALFGFALAQPQCGTKSELTKRRGIDVVVALDASKSMLARDIQPSRLERAKLELTTLLDELKGDRVGLVVFAGDAFIQSPLTSDYSAVKLFLRAVDPEVMPQGGTNVGAALRLSRQVLENADRGSKERVVVLLTDGEDLVGDVAEATEALKDAGVQVLAVGVGSESGEPIPVFDRRGAFVDYKKDAAGETVITRLDRAGLTAIAEATGGTFYFQPRGVAMSQVVERIDQMQKSELESRVTVRYDERFQSFAIPGLALLALGMLLLPSSRRRPSP
>NZ_CP017172.1|WP_140794684.1|7203856_7204867_-|VWA-domain-containing-protein
MPPLPAFNNPEALWGLLLVPLLLWQAWRERRARATLRFSAAHVFARGGRGFRTYLLPLLPLLRVAAVTAAVLAIARPQVRDSRVRDLSVEGIDIVVALDLSTSMEAGDFRPQNRMHVAKEVLSEFIANRVNDRIGLVVFAGAAYTQAPLTLDYGVLKEVVKQLRTRVLEDGTAIGDALATSLNRLRDSEAKSRVVVLITDGDNNSGKISPMDSANMAQALKVPIYTILVGKGGKVPFPQGTDLFGNTVWRDTEIPINPELMQDIADRTGGEYYRATDPEQLREGLQKVLDSLERSKLMEGGASATYREEFHPFLLAAFGLAALELLLRASFLRVFP
>NZ_CP017172.1|WP_140856604.1|7204841_7205831_-|hypothetical-protein
MNRLFPLLAVWLVVAAPAWAQPPAPAAATTDQVEPRNLSVRLEPQQVRIGDPFVYEVVITHPKDHRYELKVPQETGDFEFLDQTRQRQDGPDSATTTFRVRMSAFALGSVAVPELPFDVATPEGPKAFTVPGRTVDVTSTLPPEAEGQGADLFDYKPPEEVPIRSWRLVLTVLGVLAAALLAWVLIRWWRNRPKHVEVVPALPLDVRTRKALDALKAEDLPSRGRVKDFYFRLSEIVRGYLGERYGFEALECTSSELMASLRRMSTPGLPEDALMRFVSESDMVKYARADASADACRDALAFGYSLIDTTYVPPPPPQAPDNAAAPRVQ
>NZ_CP017172.1|WP_140794686.1|7205827_7206709_-|DUF58-domain-containing-protein
MLPKDLIRRIRKLEIRTRKVVSDMLAGQYHSVFKGRGMAFSEVRQYQPGDEIRIIDWNVTARMDEAYVKVFTEERELTVMLVVDVSASKEFGSRERTKSEIAAEVAAQIAFSAIANNDRVGLVLFSDRVEKVVPPRKGRTHVLRLVSDILTFQPQGRGTDLAAGLNYLTQVAKRKAVTFLISDFQARDYEKPLRLVGRKHDLVPVVVADPLEEAFPRLGLVDMEDPETGERFVVDTSDPRVRGRFARAMQAARDERRKLFKKLELDHVELRAGDDHGKALANFFRARARRMAA
>NZ_CP017172.1|WP_140794687.1|7206739_7207729_-|AAA-family-ATPase
MNTDIRALTERVQQESSFVEVLNQETGKVIVGQRYMLERILIGLLCNGHVLLEGVPGLAKTLTVRTVADSLSATFMRIQFTPDLLPADVVGTMIYNQQAANFTVRKGPIFANIVLADEINRAPAKVQSALLEAMAERQVTIGDQSFPLPSPFLVLATQNPIEQEGTYPLPEAQVDRFMLKVKVGYPTRDEEKVIMDRMSGGSSPRAQRVIDLQHLVRARELVHHIYMDEKVKEYILNVVFATREPSKYGLKDLADYIQFGASPRATIALAQAARAHAFLRHRGFVTPEDVKAIAFDVLRHRVAMTYEAEAEDLTPEKIIQRVFDRVEVP
>NZ_CP017172.1|WP_140876881.1|7207924_7208815_+|alpha/beta-fold-hydrolase
MKAPSVGPVEAALLAQLAPAVVATVHWLPGGGALRVLEAGAGPTVVLLHGRGGAASQWFTYLTVLARGHRVLAVDLPGFGMSSAPEGPLATGEDAAAFFTAPIEALLAQLAPGPVAVVGHSLGGLVALELALRGRVPVERLALVDAMGLGPEMARKARLFFRAGPERLARSLGPWAWAQMMPPPPTPLGERLGALEYELLTRPGASLDATRAFNRLVPVVGPAFHRAEKLGAVTAPVLLVWGEHEDTLPVSIAERAARRLPQARLLRLDAGHSPHQEHPERVLPELKAFLAVPQEG
>NZ_CP017172.1|WP_140794689.1|7209034_7209724_-|HTH-domain-containing-protein
MRRADRLFEILQVLRRAKGPMTASAIAEQLETSQRTVYRDLAALMARRVPIRGEAGVGYVLERGFDLPPLMLTPSEIEAVVLGAQWVAANADRTLSAAAGDVLAKVAAIVPKHLRELVDDPVVGTPPAKQRHPDGTVDLSRLREWSRKQLKLHIHYADAEGTTSKRTVWPILVGYVTGVRVLIAWCELRRDFRIFRTERLLSVDFLDALYPERRSTLRRRWEAQLRHTK
>NZ_CP017172.1|WP_140799652.1|7209736_7210147_-|DUF1761-family-protein
MFTLSINWFAVLLSAVALQMLGAAWFMGVIPKPYALALGRTDLMGRKPEPIFIAGPLLCGLVVTVANAILLRTFHIDAMSNALVFGAISGVGYLVATVFNVAINPNIPRPVLYGVINAPYFLLSNLVSCAILTAMA
>NZ_CP017172.1|WP_026113776.1|7210445_7210793_+|hypothetical-protein
MNHKTHERHDHVHAKGCGHPAIQHQDHVDYLHDGHLHHPHSDHTDECTLAEDARNPAQCTPQHACGAHEATHRHGPSCGHAAAPHGDHMDYLVDGHLHHPHDGHCDDHGKVQVLS
>NZ_CP017172.1|WP_140799653.1|7210866_7211253_-|thioredoxin
MATTDITKANFKEIVSKEGIVLLDWWAEWCAPCRTFAPVFEQASTKNPDLVFGKLDTDAEVELAGAFAIRSIPTLMVFRDGIMLFEQAGALPANALDDLIRQVRALDMNEVRKQLVDRQAQQGAPSQA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_15

7375400-7375513

Orphan

Consensus_repeat	Method
CGGGCCGAGGCAGCCCGGGAGCCGCCGACGGAACCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_15

>merge|NZ_CP017172|15|7375400-7375513|CRISPRCasFinder
CGGGCCGAGGCAGCCCGGGAGCCGCCGACGGAACCGCCGCATCGTCGATGCTGATGGACGCGAACGGGTCGCTCCCCGCGGGCCGAGGCAGCCCGGGAGCCGCTGACGGAACCG

>NZ_CP017172|15|14|7375400-7375513|CRISPRCasFinder
CGGGCCGAGGCAGCCCGGGAGCCGCCGACGGAACCG	CCGCATCGTCGATGCTGATGGACGCGAACGGGTCGCTCCCCG
CGGGCCGAGGCAGCCCGGGAGCCGCTGACGGAACCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_026113791.1\|7378644_7379559_+\|ArsA-family-ATPase	unknown	unknown	gnl\|CDD\|349755
NZ_CP017172.1\|WP_020478456.1\|7378170_7378476_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_162521044.1\|7361921_7362623_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_174259435.1\|7363095_7364661_+\|Hsp70-family-protein	unknown	unknown	gnl\|CDD\|212667
NZ_CP017172.1\|WP_140876952.1\|7373288_7374083_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794808.1\|7365460_7366798_-\|glutamate--cysteine-ligase	unknown	unknown	gnl\|CDD\|130503
NZ_CP017172.1\|WP_140794823.1\|7385646_7386102_+\|Holliday-junction-resolvase-RuvX	unknown	unknown	gnl\|CDD\|335420
NZ_CP017172.1\|WP_140876950.1\|7372193_7372919_-\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176506
NZ_CP017172.1\|WP_011555762.1\|7372988_7373258_+\|twin-arginine-translocase-TatA/TatE-family-subunit	unknown	unknown	gnl\|CDD\|184861
NZ_CP017172.1\|WP_140794821.1\|7383443_7383965_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140794807.1\|7364779_7365448_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794820.1\|7382121_7383315_+\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|320702
NZ_CP017172.1\|WP_140799708.1\|7366856_7367675_+\|EI24-domain-containing-protein	unknown	unknown	gnl\|CDD\|179898
NZ_CP017172.1\|WP_140876948.1\|7367889_7371114_+\|PDZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|274843
NZ_CP017172.1\|WP_140876960.1\|7383971_7385444_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794818.1\|7379555_7380671_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|223082
NZ_CP017172.1\|WP_174259436.1\|7380948_7382061_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|188247
NZ_CP017172.1\|WP_140876956.1\|7377319_7378120_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|224113
NZ_CP017172.1\|WP_174258932.1\|7371293_7372190_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140794815.1\|7376631_7377309_+\|transcriptional-regulator	unknown	unknown	gnl\|CDD\|369568

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_026113791.1\|7378644_7379559_+\|ArsA-family-ATPase	gnl\|CDD\|349755	cd02035, ArsA, Arsenical pump-driving ATPase ArsA. ArsA ATPase functions as an efflux pump located on the inner membrane of the cell. This ATP-driven oxyanion pump catalyzes the extrusion of arsenite, antimonite and arsenate. Maintenance of a low intracellular concentration of oxyanion produces resistance to the toxic agents. The pump is composed of two subunits, the catalytic ArsA subunit and the membrane subunit ArsB, which are encoded by arsA and arsB genes, respectively. Arsenic efflux in bacteria is catalyzed by either ArsB alone or by ArsAB complex. The ATP-coupled pump, however, is more efficient. ArsA is composed of two homologous halves, A1 and A2, connected by a short linker sequence.	4.83256e-39
NZ_CP017172.1\|WP_140794818.1\|7379555_7380671_+\|AAA-family-ATPase	gnl\|CDD\|223082	COG0003, ArsA, Predicted ATPase involved in chromosome partitioning [Cell division and chromosome partitioning].	3.34913e-39
NZ_CP017172.1\|WP_174259436.1\|7380948_7382061_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|188247	TIGR02795, Uncharacterized_protein_in_oprL_3'region, tol-pal system protein YbgF. Members of this protein family are the product of one of seven genes regularly clustered in operons to encode the proteins of the tol-pal system, which is critical for maintaining the integrity of the bacterial outer membrane. The gene for this periplasmic protein has been designated orf2 and ybgF. All members of the seed alignment were from unique tol-pal gene regions from completed bacterial genomes. The architecture of this protein is a signal sequence, a low-complexity region usually rich in Asn and Gln, a well-conserved region with tandem repeats that resemble the tetratricopeptide (TPR) repeat, involved in protein-protein interaction.	0.00368635
NZ_CP017172.1\|WP_174259435.1\|7363095_7364661_+\|Hsp70-family-protein	gnl\|CDD\|212667	cd10170, HSP70_NBD, Nucleotide-binding domain of the HSP70 family. HSP70 (70-kDa heat shock protein) family chaperones assist in protein folding and assembly and can direct incompetent "client" proteins towards degradation. Typically, HSP70s have a nucleotide-binding domain (NBD) and a substrate-binding domain (SBD). The nucleotide sits in a deep cleft formed between the two lobes of the NBD. The two subdomains of each lobe change conformation between ATP-bound, ADP-bound, and nucleotide-free states. ATP binding opens up the substrate-binding site; substrate-binding increases the rate of ATP hydrolysis. HSP70 chaperone activity is regulated by various co-chaperones: J-domain proteins and nucleotide exchange factors (NEFs). Some HSP70 family members are not chaperones but instead, function as NEFs to remove ADP from their HSP70 chaperone partners during the ATP hydrolysis cycle, some may function as both chaperones and NEFs.	1.30789e-105
NZ_CP017172.1\|WP_140794808.1\|7365460_7366798_-\|glutamate--cysteine-ligase	gnl\|CDD\|130503	TIGR01436, Glutamate--cysteine_ligase_chloroplastic, glutamate--cysteine ligase, plant type. This model represents one of two highly dissimilar forms of glutamate--cysteine ligase (gamma-glutamylcysteine synthetase), an enzyme of glutathione biosynthesis. The other type is modeled by TIGR01434. This type is found in plants (with a probable transit peptide), root nodule and other bacteria, but not E. coli and closely related species. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	3.31277e-115
NZ_CP017172.1\|WP_140794823.1\|7385646_7386102_+\|Holliday-junction-resolvase-RuvX	gnl\|CDD\|335420	pfam03652, RuvX, Holliday junction resolvase. This family of nucleases resolves the Holliday junction intermediates in genetic recombination.	2.84581e-64
NZ_CP017172.1\|WP_140876950.1\|7372193_7372919_-\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	4.28748e-62
NZ_CP017172.1\|WP_011555762.1\|7372988_7373258_+\|twin-arginine-translocase-TatA/TatE-family-subunit	gnl\|CDD\|184861	PRK14859, tatA, twin arginine translocase protein A; Provisional.	9.32937e-12
NZ_CP017172.1\|WP_140794821.1\|7383443_7383965_-\|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.	3.85717e-13
NZ_CP017172.1\|WP_140794820.1\|7382121_7383315_+\|M48-family-metalloprotease	gnl\|CDD\|320702	cd07343, M48A_Zmpste24p_like, Peptidase M48 subfamily A, a type 1 CaaX endopeptidase. This family contains peptidase family M48 subfamily A which includes a number of well-characterized genes such as those found in humans (ZMPSTE24, also known as farnesylated protein-converting enzyme 1 or FACE-1 or Hs Ste24), Taenia solium metacestode (TsSte24p), Arabidopsis (AtSte24) and yeast (Ste24p). Ste24p contains the zinc metalloprotease motif (HEXXH), likely exposed on the cytoplasmic side. It is thought to be intimately associated with the endoplasmic reticulum (ER), regardless of whether its genes possess the conventional signal motif (KKXX) in the C-terminal. Proteins in this family proteolytically remove the C-terminal three residues of farnesylated proteins. Ste24p is involved in the post-translational processing of prelamin A to mature lamin A, a major component of the nuclear envelope. ZmpSte24 deficiency causes an accumulation of prelamin A leading to lipodystrophy and other disease phenotypes, while mutations in this gene or in that encoding its substrate, prelamin A, result in a series of human inherited diseases known as laminopathies, the most severe of which are Hutchinson Gilford progeria syndrome (HGPS) and restrictive dermopathy (RD) which arise due to unsuccessful maturation of prelamin A. Two forms of mandibuloacral dysplasia, a condition that causes a variety of abnormalities involving bone development, skin pigmentation, and fat distribution, are caused by mutations in two different genes; mutations in the LMNA gene, which normally provides instructions for making lamin A and lamin C, cause mandibuloacral dysplasia with A-type lipodystrophy (MAD-A), and mutations in the ZMPSTE24 gene cause mandibuloacral dysplasia with B-type lipodystrophy (MAD-B). Within cells, these genes are involved in maintaining the structure of the nucleus and may play a role in many cellular processes. Certain HIV protease inhibitors have been shown to inhibit the enzymatic activity of ZMPSTE24, but not enzymes involved in prelamin A processing.	6.90008e-61
NZ_CP017172.1\|WP_140799708.1\|7366856_7367675_+\|EI24-domain-containing-protein	gnl\|CDD\|179898	PRK04949, PRK04949, putative sulfate transport protein CysZ; Validated.	4.1069e-15
NZ_CP017172.1\|WP_140876948.1\|7367889_7371114_+\|PDZ-domain-containing-protein	gnl\|CDD\|274843	TIGR03900, carboxyl-terminal_protease_family_protein, putative carboxyl-terminal-processing protease, deltaproteobacterial. This model describes a multidomain protein of about 1070 residues, restricted to the order Myxococcales in the Deltaproteobacteria. Members contain a PDZ domain (pfam00595), an S41 family peptidase domain (pfam03572), and an SH3 domain (pfam06347). A core region of this family, including PDZ and S41 regions, is described by TIGR00225, C-terminal processing peptidase, which recognizes the Prc protease. The species distribution of this family approximates that of largely Deltaproteobacterial C-terminal putative protein-sorting domain, TIGR03901, analogous to LPXTG and PEP-CTERM, but the co-occurrence may reflect shared restriction to the Myxococcales rather than a substrate/target relationship.	0
NZ_CP017172.1\|WP_140876956.1\|7377319_7378120_-\|AAA-family-ATPase	gnl\|CDD\|224113	COG1192, Soj, ATPases involved in chromosome partitioning [Cell division and chromosome partitioning].	2.14072e-53
NZ_CP017172.1\|WP_140794815.1\|7376631_7377309_+\|transcriptional-regulator	gnl\|CDD\|369568	pfam07879, PHB_acc_N, PHB/PHA accumulation regulator DNA-binding domain. This domain is found at the N-terminus of the Polyhydroxyalkanoate (PHA) synthesis regulators. These regulators have been shown to directly bind DNA and PHA. The invariant nature of this domain compared to the C-terminal pfam05233 domain(s) suggests that it contains the DNA-binding function.	9.93111e-31

>NZ_CP017172.1|WP_140876952.1|7373288_7374083_-|hypothetical-protein
MPTQEDARTVARFIHALSGGAEVRRKAAARELAWRDPLDSNELVGHLIALSRAGWGPASCALSDFMAALEQEAEHIPHVESLRRLAYVQSLDTVADLFAQGPAKLEMDADAAARADANAFSQSLGHLKQQARLTRDPDTLSRLATVSNPTVLRNVLINPRLTEELVVRIAARRPARPEPLIEIWKSPRWSVRHAIRRALVFNPYLPPETGAKIVPLLNTADLRELVSNAALHPALRAQASRLLAEGHGTGPAAASLIPGHRGHD
>NZ_CP017172.1|WP_011555762.1|7372988_7373258_+|twin-arginine-translocase-TatA/TatE-family-subunit
MACLPPPFAALCSIMLGLGLGEIIVLGFILLVVFSAARMGQLGNAVGKFVYSFRKASRGEDLVDAKPLPPGRRSTTDAEFTEPEQPRRR
>NZ_CP017172.1|WP_140876950.1|7372193_7372919_-|glycerophosphodiester-phosphodiesterase
MLLLAHRGASADAPENTLEAFAEAARQGADGVELDAMLCGSGEVVVCHDERLERLARLPWEVRLTPWWKLQRADVGSPLGFAPARIPLLEEVLEALPPQFLVNIELKCERADDGGLAEQVARLVRRRGLAGRVVISSFNPLCLFRLAAAAPELRRGLLIDPDKSWAMQAYGVSPLVSSHSVHPFHEACTPERVAAWRAAGMSVAAWTVDDPQRAHVLERMGVSYLITNRPGAVRQALHPAA
>NZ_CP017172.1|WP_174258932.1|7371293_7372190_+|hypothetical-protein
MRTFSRWVALAAWASGASVVAAPNDLQIARFGNPTGDNPVASADADFQAFARIMGAAITSVNLMPPETTGHSAWAINAELSVVSLPGSVNIPTQNEQPSTVLIPSFHARKGLPFSLELGGRVGWVEKSSQVVATGELKWAANEGFTYLPDFGVRGHVTKLFGARDLGLTVMGLDFGVGKQFPLGGMVTLTPYGGLDLGFVGATSSRIDFNPDRSFDDTTGDDSRVALTDTAAYRKVSFGSNINQRIYGGVRFIGGVLQLGAELSLTRTGSVSYEENGSTVDRGLPAVFAFNTTLGLDF
>NZ_CP017172.1|WP_140876948.1|7367889_7371114_+|PDZ-domain-containing-protein
MNQMPRFLRRITAVAVLLGAWALVGSDRAPLPLTMGAAEAGQGSWDGSLPAVKGEKAPHDLNSLRVLTKVILYVKENYVDPKRVKPKEMMIASLEYVEKSVPDVLVDGNAETGKLNVNVNGKQREFDIAHVDSLWKMSFALKDVFDFLSKNMRPIEDTRDVEYAAVNGMLSTLDPHSVLLRPELYREMKLSTKGEFGGLGFVIQMREGNLTVVKVIPKTPAHRSGIQKDDRIKKIGEESTVNMDLNEAVSKLRGPVDSRITITVERDGWDKPRIMTLSRAMISIESVQHKMLSNNVGYIRLKNFQGNTTRDLEAALTQLRKQADAKGGFKGLVLDMRGNPGGLLEQAIQVSDTFLSSGTIVATVGLSDKLREEKRARATDGEDSYPIAVLVNAGSASASEIVAGALKNLDRATIIGRQTFGKGSVQVLYDFPDDSALKLTIAKYLTPGDVSIQEVGIVPDIQLVPTRATDERVDVFAPRRSMGEADLDQHFGNPDSSTVAKKREDVLDREKPLESLKYLKVDEKQAQATAKKEESKAAPKTAANAKKHGDKDPLLDVDVAGMGEDLDDQLDAEAQEEIKEDFEVQFARDFVLRAPATTRKEQLKQGKAFIDQKRAEEESRINAAIAALGVDWSAGPTPKNVQMAVSLTPGPDAKILAGEVMEMALTAENRGTEPLKRVRAWTESDNAFLDRREFLFGALAPGEKKTWKVKVRLPKDLTSRRDDVTVRFFDDHGALPETRVAELNFVELPRPAFAFNWQVIDDCATCNGDGTVQRGETVSVLLDVTNAGTGTALDSFTQIKNGGDANIFIEKGRFKLGELKPGETKTARFQLEVKKGFKGNTFPLKLAIIDEPLEEFVMEKLELPVTDAAIATMEPKKGFVRVGDKVDLYGAPAQGARAVAKLSGTTVLPAEAVTKGYYRVELEKDRFAFVRSQDAKELKTGKATAPKATLVTNHRPPDIRLDVDPAAGGLVANGDKFTLSGVVTDPHGLLDVYVLVNDQKVYFKGVDPKGSEPNTLKFSTEFALKEGNNNVLVVAREDNDFASRRTLVIRRRPAEVAQKMASPTGSPSSKPQPQ
>NZ_CP017172.1|WP_140799708.1|7366856_7367675_+|EI24-domain-containing-protein
MSPHSTLPTISPQPRLSDFFQGMGLLGRAFSLILRDRRLFLLSALCAAVTAAALVGLVWLLWRYAPGALESVWTRPESWYGQAAWTTVLVLSGLVLWVVGANVLPPLLLAPLQDPLSELTEEACGGGPGTSFTVAGFVRGLVTGIAHTLARLFFLLAGLAVLLPLHLIPGVGSVLWTLLASLYTMTWMAGEYLAAPMTRHLYPFAEVRRMLRERRALCLGLGAGIYVLLWVPILNAFFLPVAIVAGTLLYGGLREARLLAPPPGESTTAALK
>NZ_CP017172.1|WP_140794808.1|7365460_7366798_-|glutamate--cysteine-ligase
MSLDLKRAASEPISSVDMLLAGFRAAEKPRGAHRLGLEHEKFLYPVGAAEPPTYDGERGVGALLNRVASAGYTPFRETPESPVIALQRGGATISLEPGGQVELSGSPFVTAREAHAENLTHLSEVSAAAKELGLRLVFLGYRPFGTTAQMPWMPKTRYLIMRRTLPERGRLALNMMLMTSTGQVSLDWADEADCVRKTVVVARLAPLMNALYANSPIVEGKPSGYLSFRNRVWDEVDPTRCGYLPAFFDGSFSYRAYVEWALDAPLLFLRRNNEYLYPKLTFRQLMKEGFEGKPPDLNDWTDHLSTLFPEVRLKTVIEVRGADCVNPAMTGALAALWRGILYDATALDEAERLLPKLTYAEHLAFHDTARREGLGGRLGSQELHRLAAEMLAISRRGLMRLDAQDAPLLDALDAVAASGRSPAVAVLEAWEKNPRPEALLDGFGL
>NZ_CP017172.1|WP_140794807.1|7364779_7365448_+|hypothetical-protein
MASFPVTDFPGRNAMRRSIVGGVATAALGMAGPAFAIEAQQVGERLRVEERPLVGIDVRLGLGNFTGDLGSNTKVGPLLGINASAYPWQYGGVEVGYEGQRFPIDDSRLRDNGDGEGVWRHNATLLAKAGPLIDEKWRPFVGAGVGLSYLNPSDGADRFYNNDWQTELPLAAGLDYRFGNLVAGARATYRFVGGEGLLRNPVTNADEKGSLFNGNVMIGGQF
>NZ_CP017172.1|WP_174259435.1|7363095_7364661_+|Hsp70-family-protein
MVLGIDLGTSHARVAIVQDGTPKLIPLPGTNTTDLPALIAVNGTGDLVVGAAAQTEGQRAPRRAISGLKRLLGLKPRSPQLRWLAPLLPFPVTTDTNGDSAVEVRGRVISPTLFTAMLLRELKHAAATHLGRKATRAVICAPTHFTDRQCAALREAATLAGLDAQRILIAPAAAALAYAHGRGLARKRVLVVDLGGGGLQVCVVQVTGDDLEVITTGGDATLGGMDFDARIAEAIASDLSEQGVPKPDHPLDWAPLRTAAESTKVALSSREQVDVTLPSGTVPPINRERVEALTADLAQRVTTVVRDVLESNALSPQGLDAVLLVGGQSAAPLVRRRLEESLGVSVRDDVDARGSVALGAALLGQGLLLAKAGKPAATVSEVLSSPLAVAERGGTLRRVLERNTRLPATKTLVLPTVPGPLELALFQGAATQASDAEYLGRLTLNVERAGEVELHLALSVDGALSLEATLPGVKRHAVSLATEYLDDAAFDALIARSPLIPEPERRPGGVLSGLKKLFGRR
>NZ_CP017172.1|WP_162521044.1|7361921_7362623_-|hypothetical-protein
MLVVVVDSDATPRPLFSVFGGDASSPGALPIWSSVLVVVVDSDATTEPLSSVFGAAASGSVAASLLASATGASLSGDVAAEGFVVDDASPASASCFARGSAAVAEASGAATWPASVVGSTLVVEVAVGASVGDASPALASRFSLAGATVPEGVGPASLPASVSGSTLVVDASAAARIVDVSLPLAVGSALVVADVAEDSVAASLAGAVPVAGIVAEGSLVAEVPASATIGVLA
>NZ_CP017172.1|WP_140794815.1|7376631_7377309_+|transcriptional-regulator
MSEAEQAGAPSKEPKIIKRYTNRKLYDTVESRYVTLDEIAAMIKEGTEVRIVDNRTKEDLTSVTLAQIIFEEEKKKNQMPLSVLREIIRHPGESISGFIQKEVSPRVASIREEAESRLDKLLRRDENAPRAEGEPEAPVAPPEDTTAADNAAAAGLSPADLLKASQRAFEEWQRRIDERVKHVVENLTGNLPALGRDMASLTQRLEELEKKLEQAEQQKGPPKQE
>NZ_CP017172.1|WP_140876956.1|7377319_7378120_-|AAA-family-ATPase
MRRIAFINEKGGTCKTTLAVNTAAWLAKERGLRVLLVDLDTQGHAGKALGVDVRTLPRNVFHLLTDSSVRFEDVVQRTALEGLDVLPAYKEMADFPIVVAADERRAHRLADRLRAAEAAGYDAIVFDAPPSMGTTTRNILVAATEVVVPVALTYLALDGCAEVADTVRQVGEAEGRPDLRVTKVVPTLYRKTALATAILERLKAYFPDALAATPLGYDVKVDEAQSHGQTIWEYAPRSRGAQMLAAIAAELHGEPAPKRRRASQKA
>NZ_CP017172.1|WP_020478456.1|7378170_7378476_-|hypothetical-protein
MLKNNPVMKKLVETGEERIGKLAQQLLSNEKFVAAVQTLVSRSLAAKGTLDSALRTALSAANLPSTADLEQLRSKVDDLERLLSSVEGKVDTLLAAKSPKK
>NZ_CP017172.1|WP_026113791.1|7378644_7379559_+|ArsA-family-ATPase
MAGLLDKRLWIVSGKGGVGKSTVAAALALRSARAGKRTLVCEVNTQERVSRFLERPEAGPEVAQLEQNLWAVNVRPQEAMREYGLMVLRFETLYKTVFENRLVRQFLRFIPSLQELVLLGKIMFHLQEKLPDGRWRFDTVIMDAPATGHAISFLSVPQVLIQTVPPGPMAREAQKMRDLLVDPAVTAAVLVALPEEMPVNEALELHAALRDKVSLRTHAAVLNQSFPERFTEADLEALGGHPELLAVAQAHHDRAAQAVLAGTKLERNLHAPVYPVPRLFTPEFGRKAIEQVMEHLEPLVTGAA
>NZ_CP017172.1|WP_140794818.1|7379555_7380671_+|AAA-family-ATPase
MSTTALSPALAGKRVLICVGSGGVGKTTAAAALALRASVDGRSSMVCTIDPARRLANSLGLTALGNAETRVPATALEPLGVHPRASLYAMMLDMKQTWDELITRVAPPEQRERILSNRFYQSLSTALAGSQEYISMEKLWELRRSSNYELIVLDTPPTAHALDFLDAPNRVLDFLDNDAAKWLLTPALKAGKLGMSLFNRGGYVMRGLAKFTGTEMLQELSNFMLAISSLNEGFRERARGVRQLLEDPNTGFVLVTSPHPERMDEAIHFHKMLKQHRMEVVSLVVNRVHPMPTEALWADAATLTPSRRAKVEETLREQQIMAEQDRTGIAQLQAACPGVPIVQVPRFAMDVHDISALWRTGRYLVGDETLG
>NZ_CP017172.1|WP_174259436.1|7380948_7382061_+|tetratricopeptide-repeat-protein
MAALGVVVSGCRTTGSAAREEPRATAPKQELHFDAVTVTADLELDKLNDEELFAGGTSAFAANDFQQAARYFGRLVDFFPDSRHRRAALYNAGLAHQRLKEWEEAGHRFSELSDPAKGQGDALDAAFRVAEVDYHLERFEQASKLLGIIAAREDLPLNRRLEAQVQQGICQLESGSPETAEVTLRKALSTYDALEDKGEVDDYFPAQAHFFIGELYRLHYDGVKLDPAKGADKLAQDLNYKAELLLSAQGHYLRSIRVGNGYWATAAGTQIGSLYENLYEHMVNSPAPAELDASEAEIYRQELRKKIRVLLTKSITIYERTLETAERIGSQSTFVDRTRESLAKVKALLLADAEGEPASAAPSSEREPHT
>NZ_CP017172.1|WP_140794820.1|7382121_7383315_+|M48-family-metalloprotease
MEPLFTPEQLAEIHAFHQPYYIRAAVGPFANLALMLLMLGVLVQPLHRLAVAAAAGLERRLGFLRAAPVSRAFFRAMDRLWGEPGWGAAVLFALFTDLFVSLVYLPVDVWFSYTLEHRHGMSTQTPATFAYDMVKAQLLAAFAISALVIGMFGLARKLRQWWLVLGVPVALLLLVSGALDPYRSRLFFNQKPLPEGPLRTRIVDLMEQADIAFADVLVEETSVASRRLQAYFAGQGPTRTIVLNDIILKELSEDEVLAAVAHEAGHVNESKWPARIASSLMLVALLFALDRLLRLSASRGWFGATHFADIRNLPLISLLFFLLVLTAKPLSGAFSREREREADRYALRLTGDVDAFRRMLVKAARVNKMDPEPPRWVVLKGMSHPPIGERIASLPTP
>NZ_CP017172.1|WP_140794821.1|7383443_7383965_-|tetratricopeptide-repeat-protein
MGRIIKHEGAVAMRMQRGAVQGLKAFARGEATWAEVEGMTFEEAKAIAQVGCDLAAAGRLEEARILFEGLVEGNPKDAAARAALGTVYQKLGKLEDAIAEYSAALEREPDNPVALANRGELYLRKGERQGFTDLANAVEADPHGETAGGRRARALVKAITLVAVEKLKENSQP
>NZ_CP017172.1|WP_140876960.1|7383971_7385444_-|hypothetical-protein
MLDFLKGAANLLAGPMSTAVDFAGNALGLPPLITNSIKTAAGVATGNVMLAASGAMGVAQELSKNPPAKTEYHSSSSGNSKADSGYAPSASSSPILNPGSSPLDPKMLDYSDALKVLEANFQQLDLLDGTKSGSLSKKDLQRISTDSNLSPQLRDAARFMVDNTALFERLDRQGPLARIGVFSPLYNLDTFSVKDLQRELKSVDAEFARYGRPVRPGSGGTTPPGTGCTPGGGGTTAPGTGGTSGGGGSAPVPGSPPTSTASPLDPDFHEYHDALRVLNANWDTFDTAVGARDNVLTRDNLDAILNSPAASSTLKRAAQFFKDHPAYYDRLEMAAGVGPRDGIVGRPDVTAALRQADAAQASSGTSSTNGSGGSRPVGGASSNVRSIVDNPNMSIEDKIQAILMSISSDTDEEILDVMEQMANVREQRASLGNGESDRKAGAKLESSMQELELRLQRLVEKRKAMFDLMSNMSSKFHEMAKTAISNLRSA
>NZ_CP017172.1|WP_140794823.1|7385646_7386102_+|Holliday-junction-resolvase-RuvX
MRTMGLDLGTKTIGVAVSDGLGLTAQGVTTVRRTSLKADLAALATVASEHEVTHVVLGLPLNMDGSEGPRAEASRKFADTLTQSLGVTVELWDERLSTVAATRTLLEADVSRARRREVIDQVAAQFILQGWLDAHRPPDTDYHPDDYDSEP

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_16

7530332-7530428

Orphan

Consensus_repeat	Method
ACGTGCAGGACCTGCTGGCCGCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_16

>merge|NZ_CP017172|16|7530332-7530428|CRISPRCasFinder
ACGTGCAGGACCTGCTGGCCGCGAAGTTCGTCTGATGCGAGGGCCGCGGAGGGCCGCCGCGCGGTCCTGCTGAACGTGCAGGACCCGCTGGCCGCGA

>NZ_CP017172|16|15|7530332-7530428|CRISPRCasFinder
ACGTGCAGGACCTGCTGGCCGCGA	AGTTCGTCTGATGCGAGGGCCGCGGAGGGCCGCCGCGCGGTCCTGCTGA
ACGTGCAGGACCCGCTGGCCGCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140799765.1\|7534833_7536075_-\|diaminopimelate-decarboxylase	unknown	unknown	gnl\|CDD\|143501
NZ_CP017172.1\|WP_011555871.1\|7526262_7527060_-\|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	unknown	unknown	gnl\|CDD\|224997
NZ_CP017172.1\|WP_140877013.1\|7522441_7523497_-\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|223769
NZ_CP017172.1\|WP_174257122.1\|7519149_7520616_+\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP017172.1\|WP_140799763.1\|7532307_7533078_-\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP017172.1\|WP_011555870.1\|7525260_7526226_-\|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	unknown	unknown	gnl\|CDD\|224936
NZ_CP017172.1\|WP_140877011.1\|7521344_7522322_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|274995
NZ_CP017172.1\|WP_140794915.1\|7528503_7529175_-\|fructose-6-phosphate-aldolase	unknown	unknown	gnl\|CDD\|234947
NZ_CP017172.1\|WP_140794918.1\|7531786_7532311_-\|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase	unknown	unknown	gnl\|CDD\|223872
NZ_CP017172.1\|WP_140877015.1\|7530449_7531790_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP017172.1\|WP_140794926.1\|7539285_7540110_+\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|320692
NZ_CP017172.1\|WP_140799768.1\|7538207_7539080_-\|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	unknown	unknown	gnl\|CDD\|234899
NZ_CP017172.1\|WP_140794913.1\|7524529_7525183_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370070
NZ_CP017172.1\|WP_140794909.1\|7520713_7521307_-\|MOSC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377051
NZ_CP017172.1\|WP_140799767.1\|7536322_7538131_-\|TIGR04551-family-protein	unknown	unknown	gnl\|CDD\|275344
NZ_CP017172.1\|WP_140799761.1\|7527177_7528314_-\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|173847
NZ_CP017172.1\|WP_140877017.1\|7533074_7533890_-\|4-hydroxy-tetrahydrodipicolinate-reductase	unknown	unknown	gnl\|CDD\|234595
NZ_CP017172.1\|WP_140794912.1\|7523497_7524475_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP017172.1\|WP_140877019.1\|7533929_7534817_-\|4-hydroxy-tetrahydrodipicolinate-synthase	unknown	unknown	gnl\|CDD\|235107
NZ_CP017172.1\|WP_174259358.1\|7536071_7536320_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|215397

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140799765.1\|7534833_7536075_-\|diaminopimelate-decarboxylase	gnl\|CDD\|143501	cd06828, PLPDE_III_DapDC, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Diaminopimelate Decarboxylase. Diaminopimelate decarboxylase (DapDC, EC 4.1.1.20) participates in the last step of lysine biosynthesis. It converts meso-2,6-diaminoheptanedioate to L-lysine. It is a fold type III PLP-dependent enzyme that contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. DapDC exists as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Homodimer formation and the presence of the PLP cofactor are required for catalytic activity.	0
NZ_CP017172.1\|WP_011555871.1\|7526262_7527060_-\|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	gnl\|CDD\|224997	COG2086, FixA, Electron transfer flavoprotein, beta subunit [Energy production and conversion].	1.45372e-84
NZ_CP017172.1\|WP_140877013.1\|7522441_7523497_-\|EamA-family-transporter	gnl\|CDD\|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	1.20355e-16
NZ_CP017172.1\|WP_174257122.1\|7519149_7520616_+\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	2.07458e-12
NZ_CP017172.1\|WP_140799763.1\|7532307_7533078_-\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	1.94315e-93
NZ_CP017172.1\|WP_011555870.1\|7525260_7526226_-\|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	gnl\|CDD\|224936	COG2025, FixB, Electron transfer flavoprotein, alpha subunit [Energy production and conversion].	3.40322e-111
NZ_CP017172.1\|WP_140877011.1\|7521344_7522322_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|274995	TIGR04122, hypothetical_protein, putative exonuclease, DNA ligase-associated. Members of this protein family frequently are found annotated as a putative exonuclease involved in mRNA processing. This protein is found, exclusively in bacteria, associated with three other proteins: an ATP-dependent DNA ligase, a helicase, and putative phosphoesterase.	5.02553e-70
NZ_CP017172.1\|WP_140794915.1\|7528503_7529175_-\|fructose-6-phosphate-aldolase	gnl\|CDD\|234947	PRK01362, PRK01362, fructose-6-phosphate aldolase.	2.57828e-151
NZ_CP017172.1\|WP_140794918.1\|7531786_7532311_-\|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase	gnl\|CDD\|223872	COG0801, FolK, 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase [Coenzyme metabolism].	2.50847e-55
NZ_CP017172.1\|WP_140877015.1\|7530449_7531790_-\|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.	0.000145272
NZ_CP017172.1\|WP_140794926.1\|7539285_7540110_+\|M48-family-metalloprotease	gnl\|CDD\|320692	cd07333, M48C_bepA_like, Peptidase M48C Ste24p bepA-like, integral membrane protein. This family contains peptidase M48C Ste24p protease bepA (formerly yfgC)-like proteins considered to be putative metallopeptidases, containing a zinc-binding motif, HEXXH, and a COOH-terminal ER retrieval signal (KKXX). They proteolytically remove the C-terminal three residues of farnesylated proteins. They are integral membrane proteins associated with the endoplasmic reticulum and golgi, binding one zinc ion per subunit. In eukaryotes, Ste24p is required for the first NH2-terminal proteolytic processing event within the a-factor precursor, which takes place after COOH-terminal CAAX modification (C is cysteine; A is usually aliphatic; X is one of several amino acids) is complete. Mutation studies have shown that the HEXXH protease motif, which is extracellular but adjacent to a transmembrane domain and therefore close to the membrane surface, is critical for Ste24p activity. Several members of this family also contain tetratricopeptide (TPR) repeat motifs, which are involved in a variety of functions including protein-protein interactions. BepA has been shown to possess protease activity and is responsible for the degradation of incorrectly folded LptD, an essential outer-membrane protein (OMP) involved in OM transport and assembly of lipopolysaccharide. Overexpression of the bepA protease causes abnormal biofilm architecture.	2.78267e-68
NZ_CP017172.1\|WP_140799768.1\|7538207_7539080_-\|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	gnl\|CDD\|234899	PRK01103, PRK01103, bifunctional DNA-formamidopyrimidine glycosylase/DNA-(apurinic or apyrimidinic site) lyase.	3.00502e-82
NZ_CP017172.1\|WP_140794913.1\|7524529_7525183_+\|hypothetical-protein	gnl\|CDD\|370070	pfam08695, Coa1, Cytochrome oxidase complex assembly protein 1. Coa1 is an inner mitochondrial membrane protein that associates with Shy1 and is required for cytochrome oxidase complex IV assembly. It contains a conserved hydrophobic segment (amino acids 74-92) with the potential to form a membrane-spanning helix. The N-terminus of Coa1 is rich in positively charged amino acids and could form an amphipathic alpha helix, characteristic of a mitochondrial presequence. A cleavage site for the mitochondrial processing peptidase is predicted adjacent to the presequence. Upon in vitro import into mitochondria, Coa1 is processed to a mature form, indicating that it possesses a cleavable presequence. The eukaryotic cytochrome oxidase complex consists of 12-13 subunits, with three mitochondrial encoded subunits, Cox1-Cox3, forming the core enzyme. Translation of the Cox1 transcript requires the two promoters, Pet309 and Mss51, and the latter has an additional role in translational elongation. Coa1 is necessary for linking the activity of Mss51 to Cox1 insertion into the assembly complex.	1.19074e-09
NZ_CP017172.1\|WP_140794909.1\|7520713_7521307_-\|MOSC-domain-containing-protein	gnl\|CDD\|377051	pfam03473, MOSC, MOSC domain. The MOSC (MOCO sulfurase C-terminal) domain is a superfamily of beta-strand-rich domains identified in the molybdenum cofactor sulfurase and several other proteins from both prokaryotes and eukaryotes. These MOSC domains contain an absolutely conserved cysteine and occur either as stand-alone forms or fused to other domains such as NifS-like catalytic domain in Molybdenum cofactor sulfurase. The MOSC domain is predicted to be a sulfur-carrier domain that receives sulfur abstracted by the pyridoxal phosphate-dependent NifS-like enzymes, on its conserved cysteine, and delivers it for the formation of diverse sulfur-metal clusters.	1.86535e-06
NZ_CP017172.1\|WP_140799767.1\|7536322_7538131_-\|TIGR04551-family-protein	gnl\|CDD\|275344	TIGR04551, hypothetical_protein_CAP_1272, TIGR04551 family protein. Members of this family are proteins of unknown function, about 620 amino acids in length, and universal in but restricted to the Myxococcales, an order within the Deltaproteobacteria with at least 15 sequenced genomes as of 8/2014. The most closely related homologs outside the Myxococcales show localized homology only and display sharply lower scores. Relatively few protein families (roughly 20) could be built to have a comparable restriction to the Myxococcales. The putative protein sorting signal MYXO-CTERM (TIGR03901) appears so far universal in but restricted to the Myxococcales, making the present family a candidate to be involved in recognizing and processing proteins with that signal.	0
NZ_CP017172.1\|WP_140799761.1\|7527177_7528314_-\|acyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|173847	cd01158, SCAD_SBCAD, Short chain acyl-CoA dehydrogenases and eukaryotic short/branched chain acyl-CoA dehydrogenases. Short chain acyl-CoA dehydrogenase (SCAD). SCAD is a mitochondrial beta-oxidation enzyme. It catalyzes the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of SCAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. This subgroup also contains the eukaryotic short/branched chain acyl-CoA dehydrogenase(SBCAD), the bacterial butyryl-CoA dehydorgenase(BCAD) and 2-methylbutyryl-CoA dehydrogenase, which is involved in isoleucine catabolism. These enzymes are homotetramers.	2.029e-170
NZ_CP017172.1\|WP_140877017.1\|7533074_7533890_-\|4-hydroxy-tetrahydrodipicolinate-reductase	gnl\|CDD\|234595	PRK00048, PRK00048, dihydrodipicolinate reductase; Provisional.	2.3062e-113
NZ_CP017172.1\|WP_140794912.1\|7523497_7524475_-\|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.	7.84318e-10
NZ_CP017172.1\|WP_140877019.1\|7533929_7534817_-\|4-hydroxy-tetrahydrodipicolinate-synthase	gnl\|CDD\|235107	PRK03170, PRK03170, dihydrodipicolinate synthase; Provisional.	2.60634e-152
NZ_CP017172.1\|WP_174259358.1\|7536071_7536320_-\|hypothetical-protein	gnl\|CDD\|215397	PLN02744, PLN02744, dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex.	0.002301

>NZ_CP017172.1|WP_140794915.1|7528503_7529175_-|fructose-6-phosphate-aldolase
MKFFIDSADVEEIRKAHAMGCVDGVTTNPSLLAKVGRGLEETIREICSIVDGPISAECVSMEADELIKEGRSLAKIHDNVVVKIPMGVEGMKATKALTAEGIRTNVTLCFSANQALLCAKAGATYVSPFVGRLDDISQDGMELISHILEIYRNYEHFNTQVLVASVRNPVHVLQAARLGADVATLPYNVITQLANHPLTDAGIKKFLADWEKVPKAAKPPASK
>NZ_CP017172.1|WP_140799761.1|7527177_7528314_-|acyl-CoA-dehydrogenase-family-protein
MEFQLTDAQRALQDAARKFAREVVRPKAAHYDETATFPLDLLTTAWELGLLNMAIPAEYGGVGLSHLDQTIVAEELSWGCAGVATSIIANDLANLPIILHATEEQKKRLLTPFTEKLKFSSFCLTEPEAGSDVANMQTTARLDGDHYVLNGAKCFITNGGQASQYTVFATVDKGRKHKGITCFVVEGRPEGLSVSKHENKMGQRASETVSLTFEDVRVPVANRIGEEGQGFAIAMATLDNSRPLTAMFSVGIARAALEHSMEYSTQRRTFGKPIIEHQAIQFMIADMAMNTHAARMLTYESAWLLDEGKRNSLQSSYAKCFAADMAMKVATDAVQVYGGYGYIKEYPVEKLMRDAKLIQVYEGTSQVQRLVIARELFK
>NZ_CP017172.1|WP_011555871.1|7526262_7527060_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein
MKILVTAKRVEDPESKIKVKPDGSGIVQEGLKYKINPFDEIGVEEGLRLVAKHQGEVVVVSIGGKEVQEQLRHALAMGAHRAVWVNHTGPVDQLGIAALLQKVVEKEQPDLVILGKQSIDDDQNQVGQYLAEFLGWGQATFASKVESMESEQEKNKVPAIVVSADKKSVQVIREVDNGLATVECQLPAVVTTDLRLNQPRYASLPGIMKAKSKPIEELTPAKLSVDVTPAIQVLKMSAPPARKAGIKVADVPALVEKLHNEAKVV
>NZ_CP017172.1|WP_011555870.1|7525260_7526226_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein
MPIVLIVAEQQPDGNLRKATLNAISAGKQLAEKAGGELHIALVGKDPSKVADELKGYGAKAVHLGAAAELEHYLAETYAPAIAALAQELKADYIGMASTAQGKDLLPRVAGRLRAAMATDVMAINGSGADITFTRPMWAGNVFADVKLTTPVKVLTLRATEFPAAAGGQGAAEVKTFSPKVEASKTKFVDFKEVKSARPELTEARVVISGGRGTKGDFKEIEGLADDLGAAVGASRAVCDAGWVPNDLQVGQTGKVVAPALYIAAGISGAIQHLAGMKSSKTIVAINKDPEAPIFQVADYGMVADLFKVLPELRAELAKLK
>NZ_CP017172.1|WP_140794913.1|7524529_7525183_+|hypothetical-protein
MPGTHTNRWRCRTASTRSPRASGANKRKPRAKWEEVAMDTAQEGSMAPRPGWWSRHWRWVLPLGCLGLLASCIGLGVLATYLGFSSLGQSDAHREAVAIASGDALVQRALGTPIESGLPRRSSVQSRNGVSRAQFSLPLEGPDGKGTLHAQGEKRGDGPWQFNNLIVALSDGTLIDLLRAEPLKRPELPLPAEPPYADQAPEPGKVAPRDAGRDIEL
>NZ_CP017172.1|WP_140794912.1|7523497_7524475_-|GNAT-family-N-acetyltransferase
MPSRRSSSAEVLLDVLEALPPGHRLWVRGAGRSLFPLLRAGDSVRVMRCGPGSLATGDVALMRQGRELVAHVVVSTQPWRTASLLGPQDAPGGVTLGRVVAIRRGRWVVPLPRPLRPALRLAQQAASTAWAWPRTRIVSRGVWDFLFAGWSLPLRRRLVGPLEVRLLTAGDLDPLLAFASERLVVSPGFLRRQLRERWGLPDAGRRGAAAGAFDAQGRMHGFAWVDSYRQEGLHLEGVWVRSLVVAPRVRRMGVATGLLECLMEEARRQGQSHVFADVDDDNTASLRTFERLAFRRADATLTQQANEAWDATGRSKRLVVVERTL
>NZ_CP017172.1|WP_140877013.1|7522441_7523497_-|EamA-family-transporter
MRLRRLRGRPGCVKKPAAVAAVTSRGEPGVILSDGLRAMSTSTSDMLGGATETPSRSQRLRADGALALITSFWGITFVVVKDALGHGDPFSFLTLRFIVGAVVLSALAGRQVLTARNLRSGTMLGTFLFLGFSLQTVGLTTTTPSRSAFITGLCVLLVPLLSMVLYRKAPKFTSLLGVGVAAVGLYLFTQPDAGLGSGGLSSGDVLSLGCAVAYACHILMTERHAPKQGVLGLVAVQLWTVALLSALCLPFVERRVVWHPSFVGAVLVCGVFASALAISLQTWGQARTTAVRAALIYSLESVFAALYSVLLGYETLGPREWLGGALILSGVLMSEVGAAAWGWWRARAPAR
>NZ_CP017172.1|WP_140877011.1|7521344_7522322_-|MBL-fold-metallo-hydrolase
MSVELRRNGMHLTGTPLSLDAKRKSPLCFVSHGHSDHIARHESTIATAATLRFMTHRLGPVREPREVPFRQPFELGPLVLELLPAGHILGSAQLRVTWPDGRRIVYTGDLNVAPSLTAEATEVAECDTLVIESTFGHPRYRFPPRPEVLGQVEQWLRMQLERGAVPVLLGYPLGKSQEAMKHLAGRGFPLVAHSSIYEVAQLYAELGVPIENLRCYDGKVEPGEVLFFPPHHARGGALAPLWPRATAVLTGWAVDRGAVRRYGADVAFPLSDHADFPGLVSYAKATGAREVLTCHGFAEELAQALRDAGMDARPLGGKPQQLGLF
>NZ_CP017172.1|WP_140794909.1|7520713_7521307_-|MOSC-domain-containing-protein
MARKTPQLEGRIVHVLVCTERKSFVTKELPEARVSFEGLEGDRHAGLTRAADVRTPWFPKGTPIRNTRQFSLVSSEELAQVAQALGIPRVLASWLGANLEVAGVPRLTHLPPGTRLFFPEDATLVVEGENEPCTGPGRVIEAHHPDVQKLASRFVKAAWQRRGLVAWVERPGIIRAGDTVKVLLPRPVTYMLPSSGV
>NZ_CP017172.1|WP_174257122.1|7519149_7520616_+|pentapeptide-repeat-containing-protein
MAKAQSIEKLLQSGSAEWNRMRKSGQVATDHTGATFTQLFSANTDLSGLGLIGSEWDRCDLSKVNFRDADLSNAYFHGGRLQDCDFRGANLEGATFEKLKLLRCDFTGAKGLDDIEMDDVDMDRVVGLDGEEAPPPPPPPAQGITAFTREQREKALGVQAAAALQGEPVGDELPPFRPQDPPGSLFFRALKRMGVPPLWVLDVPGLRPLLPQRLPPGSSLETLYREAVKTRLENKKPAADPAVVDRAQKALRMGAKDAPVAAMYLREVGVLPLFRFSAAQVLKGALREEVEVDDLTGSIDPRTTGALLELRLTHEVVEHLQEARRRLAATQLYTSLLEAGFNPENNWDEALESSDASMELAQLATGEDRNALLEGFQVFAALPDEARLRRLAYLAESVTNLELVSRLPEGMEPSWLTGPETRECHEREMTYVQSLKAEEIPAKVAALAKEELGVPEGEVPEESDGDLFVHLRCDVCGKEKLIVQSPEE
>NZ_CP017172.1|WP_140877015.1|7530449_7531790_-|hypothetical-protein
MNLPLALATAALLTAEPSTLPPGHPVIPPGTTASPATSGMPEGHPPTGGVAPSINPEQLPPGHPPMSGTGRAPPSAEELLRQLDSTEGLADREKTFEIAASLGRLYYVNGRNAEASTYLQQALERAKPTRELFLAQRKKLGKAAVPTPEAAGCGFTPNMPVEDMGAAAQARAKKGDAAGAAACARAALAPVLDVAVMQANALYLSNDSGKALVAYDAVLDVEPLHEDALYARAALLFETKGDDVAALKKAGEGFEAVATTYPDSFRAPMAKRMVALVEETVKAGGRKQLLASRAEDRRIRLSQAPAAATPDAPRPLSQEMVDAVKNTERTPELEQGLAKLVDEGEELLAKGQYQEALANYTRVVPFQPENGRAKAGMAWSLVSLERPMAARVWGVAVQTDPLSVEKLGDALKAKGDDKGAKALWEKLATDAPDYPNKASLQAKLGK
>NZ_CP017172.1|WP_140794918.1|7531786_7532311_-|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase
MSDTVYVGLGSNEGERENHLVAALSALSRIDAVAVLHCSSLFDSAPVGPPQPRFLNAVVALECGLPPQRLLCILQQIEKDLGRRRDVRWGPRTIDLDILFWEGQVVADPSLQVPHLELHKRRFALEPLVELAPHLRHPVLGMSVKELLGKLAPQDVRRSEATWWPEASYSSNDT
>NZ_CP017172.1|WP_140799763.1|7532307_7533078_-|fumarylacetoacetate-hydrolase-family-protein
MTTARYCRFLHEGRAHHGRVEGSEVAVLTAAPWAGAKETGIHRSLSSLTLLVPSDASKVVCIGQNYRKHAEEMGKPVPPEPLIFTKPSTALNGTGSPIRIPKASQEVHYEAELALVIGEKLKNADESTAARAIWGLTCFNDVTARDVQRREIQHTRAKGYDTFACAGPWAVTGLSPDDLHIVCRVNGQVRQDSRTSDMIFSPARLVSFISHIMTLLPGDIVSTGTPSGVGKLSAGDTVEVELEGIGTLVNPVEMEP
>NZ_CP017172.1|WP_140877017.1|7533074_7533890_-|4-hydroxy-tetrahydrodipicolinate-reductase
MIRTVITGITGRMGSTLLRLARDSGDLRVVGGTARPGSALVGQDAGVATRLGPVDVTVVDSLERALDAAQADVVIDFTSAELSVAHAKVCAARGVALVVGSTGFTPEASASLAESAKTVPIVAAPNMSVGVNLVIRMAAELARVLGPGFDVEVLEAHHRMKKDAPSGTALRLADVLAEALGRTQEDLTFARHGQIGARPAREIGVQTLRGGDVVGEHTVYFLGEGERIELTHRATNRDQFAAGALRAARWVAGRAPGLHDMADVLGFQRTS
>NZ_CP017172.1|WP_140877019.1|7533929_7534817_-|4-hydroxy-tetrahydrodipicolinate-synthase
MKTFEGSMTALATPFRNGALDEPAYRALVRQQIEGGTSVLVPMGTTGEAVTMTADERARAVKVVVEEAKGRVTVVGGAGSNSTAETIEGVRRVRDAGADGTLIVTPYYNKPTQAGLLEHYRAVAKAHPGFPIIAYNVPGRTGVDLLPDTVLRLCDIPEVVALKEATGSMPRAIDILEKCGDRMTLLSGDDFTVLPFIACGGKGVISVSSNVAPRMMADLVAAARAGNIAVARDLQLRMNELHRLLFIESSPTPVKWGLHVMGLFGPEVRLPLVQMTEPNAAKLRDTLRQLGLLTG
>NZ_CP017172.1|WP_140799765.1|7534833_7536075_-|diaminopimelate-decarboxylase
MNHFAYRKGVLHAEDVPLAAIAESVGTPTYVYSTATLTRHVRVVTEAFGDRPHLICYSVKANSNLAILRLIAERGGGFDIVSGGELARVRHVGGDTAKTVFAGVGKTQEEMEAALAAGILLFNVESAEELEALDAVGRRLGRRAPFALRVNPDVDARTHRYISTGLKTSKFGVPFEEAVALYARAKKMKGLLAAGLDCHIGSQLTQTAPIRAALSKVAGLYSALKEKGHPLAYLDVGGGLGITYSDETPPSPDEYARTVMAAAGATGATLILEPGRALMGNAGVLLTRVLYRKKTPARHFVVVDAGMNDLLRPALYEAHHGLQPLMKRRGKAVEVDVVGPVCESTDVLAKARPLVLPQAGELFAIMSAGAYGMSMSSTYNSRPRPAEVLVDGEAWRVVRERERVEDLWRGERA
>NZ_CP017172.1|WP_174259358.1|7536071_7536320_-|hypothetical-protein
MRQVLARLCVAASVSLTLAACGIKGPPRPPGPPPAPATQTQPPPPESERGPLEPSGPTLSPTPETGVETPLSPPESEDAGVP
>NZ_CP017172.1|WP_140799767.1|7536322_7538131_-|TIGR04551-family-protein
MSHALLAALLVASSTATAQTPVPEGSPPAPAEAAPAAPAPAESVSAETAPVSSTREGVSRDDLEALKEELREEIRAEAAKQSIGATDEWAEEFPEEKRKLEVFTLDGYFRVRPTLFYKFDLGKAPGKELFPRSPRSAQENTQSFATMRVRLAPTFNISEQVALKMEVLGLDNFIMGAMPDTLLPGNTRNLFGIFSESQDPLADALQDSIKLRRAYGEVKTPVGILRFGRMGSQWGLGMLRNDGTCFDCDFGDTVDRVQFVTNPFEGWYVTPMLDFNSEGVTDTRGTVGEPIDLTQSDDAHSWVIAIARRDTDQVIRSKLDNNQGVLQYGLHFTYRTQKWEYDGSTTNGQNTGFIPRDASLFVPDLWLKYEEKNWRLEFEAAAQLGRIGNRALDVGGINDPTLNQSLTVAQFGGVAQGELRLLNQKLSLNMELGFASGDKAPGFGNQPSRPGSGTNGRTEPGDFEGPQYDCGTGGCRDNAIRNFRFNRDYRIDLILWRELLVGVTDAFYVRPSAKYTITEGFDIYGRVIYSQAMYAQSTPSFTNKALGLEVNVGADYKTEDGFIAGIAYGILFPMSGLREFNATVPTDLDTPQTIRAWLGMQF
>NZ_CP017172.1|WP_140799768.1|7538207_7539080_-|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase
MPELPEVEIARRNLVRWFSDRRLVRAESENTRIFRGAERQQFDTLTGRLESLVRRGKYLLFAFEGGKGLMGHLGMTGKFVRRTEGQVAPYSRARFHLDDGHVIHFSDPRMFGRLEPAPAARLRELEAVRILGRDPLADGLTAGQLQQAVGSSRKELKVALMDQERISGLGNIHAAEALFRAGLHPSRQPGSLTPDEWKRLVQAIRASIDFGLKEQEGEEPVYLEEGRSENPFRVYGRAGSPCSQCGTRVESFTQGGRTTHYCPRCQPGDGRRSEAGSPAVDGAKARPGKR
>NZ_CP017172.1|WP_140794926.1|7539285_7540110_+|M48-family-metalloprotease
MQRILVAVLGVTLALGLSTGCTKQRISAEKAVARTLISDEQEEQLGKQVKAELETKEKIKYVQNAAVVDYVRGISASILNQASKDRPGVKWKINVIDDPKMVNAFATPGGYLYVYTGLILAADTEAELAGVMAHEAGHVVGRHSARAMVNQMGLQAITQAALGQNPGTVAQIAASLVSGGTLLAHGRGEEIEADEYGARYASGAGYDPRGLITFFEKLQKEQGDTPALMKWLSTHPTNRDRIANIQKIISQKNLRGSNNGPGGLPAIKQALGGK

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_17

7898362-7898531

Orphan

Consensus_repeat	Method
CTCCACGGGGCCCATGCGCGTCTCCTCGG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP017172_17

>merge|NZ_CP017172|17|7898362-7898531|CRISPRCasFinder
CTCCACGGGGCCCATGCGCGTCTCCTCGGTGAGCGGCTCCACCGGGCCCATGCGCGTTTCCTCGAAGCGAGGCTCCACGGGCCCCATGCGCGTCTCCTCGGGGCGCGTGAGGAGCGGAATGTCCCGCGTCGCGTCCTCGTCCTCGTCCGGGGCGATGCGTGGCTCCTCGG

>NZ_CP017172|17|16|7898362-7898531|CRISPRCasFinder
CTCCACGGGGCCCATGCGCGTCTCCTCGG	TGAGCGGCTCCACCGGGCCCATGCGCGTTTCCTCGAAGCGAGG
CTCCACGGGCCCCATGCGCGTCTCCTCGG	GGCGCGTGAGGAGCGGAATGTCCCGCGTCGCGTCCTCGTC
CTCGTCCGGGGCGATGCGTGGCTCCTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140795161.1\|7884358_7884643_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140877230.1\|7890884_7892393_-\|tail-fiber-domain-containing-protein	unknown	unknown	gnl\|CDD\|240612
NZ_CP017172.1\|WP_140795174.1\|7900373_7900553_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140795164.1\|7887098_7889102_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP017172.1\|WP_174258951.1\|7907860_7909153_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|379114
NZ_CP017172.1\|WP_140795173.1\|7898664_7900377_-\|sodium:solute-symporter	unknown	unknown	gnl\|CDD\|271385
NZ_CP017172.1\|WP_140877245.1\|7910340_7911477_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|334462
NZ_CP017172.1\|WP_140877240.1\|7904797_7905604_+\|bacillithiol-biosynthesis-deacetylase-BshB1	unknown	unknown	gnl\|CDD\|274915
NZ_CP017172.1\|WP_140795170.1\|7894523_7895174_+\|SRPBCC-family-protein	unknown	unknown	gnl\|CDD\|176860
NZ_CP017172.1\|WP_140877232.1\|7895330_7897481_+\|catalase	unknown	unknown	gnl\|CDD\|236886
NZ_CP017172.1\|WP_140795163.1\|7886252_7886936_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP017172.1\|WP_140877243.1\|7909408_7910344_+\|proline-racemase-family-protein	unknown	unknown	gnl\|CDD\|172473
NZ_CP017172.1\|WP_140795178.1\|7905600_7906764_+\|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA	unknown	unknown	gnl\|CDD\|274914
NZ_CP017172.1\|WP_174259366.1\|7903127_7904801_+\|bacillithiol-biosynthesis-cysteine-adding-enzyme-BshC	unknown	unknown	gnl\|CDD\|274913
NZ_CP017172.1\|WP_140795169.1\|7892984_7894400_+\|L-serine-ammonia-lyase	unknown	unknown	gnl\|CDD\|273233
NZ_CP017172.1\|WP_140877236.1\|7900549_7903033_-\|PIG-L-family-deacetylase	unknown	unknown	gnl\|CDD\|376836
NZ_CP017172.1\|WP_140795166.1\|7889981_7890806_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140799897.1\|7884786_7886178_+\|ammonium-transporter	unknown	unknown	gnl\|CDD\|223083
NZ_CP017172.1\|WP_140795179.1\|7906784_7907642_-\|DUF2911-domain-containing-protein	unknown	unknown	gnl\|CDD\|378565
NZ_CP017172.1\|WP_140795165.1\|7889016_7889967_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140877245.1\|7910340_7911477_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|334462	pfam01266, DAO, FAD dependent oxidoreductase. This family includes various FAD dependent oxidoreductases: Glycerol-3-phosphate dehydrogenase EC:1.1.99.5, Sarcosine oxidase beta subunit EC:1.5.3.1, D-alanine oxidase EC:1.4.99.1, D-aspartate oxidase EC:1.4.3.1.	2.02977e-50
NZ_CP017172.1\|WP_140877230.1\|7890884_7892393_-\|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.	1.2186e-20
NZ_CP017172.1\|WP_140795164.1\|7887098_7889102_+\|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.	4.98732e-103
NZ_CP017172.1\|WP_174258951.1\|7907860_7909153_+\|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_CP017172.1\|WP_140795173.1\|7898664_7900377_-\|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_CP017172.1\|WP_140877240.1\|7904797_7905604_+\|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].	3.62069e-115
NZ_CP017172.1\|WP_140877236.1\|7900549_7903033_-\|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.	5.73134e-21
NZ_CP017172.1\|WP_140877232.1\|7895330_7897481_+\|catalase	gnl\|CDD\|236886	PRK11249, katE, hydroperoxidase II; Provisional.	0
NZ_CP017172.1\|WP_140795163.1\|7886252_7886936_-\|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_CP017172.1\|WP_140877243.1\|7909408_7910344_+\|proline-racemase-family-protein	gnl\|CDD\|172473	PRK13970, PRK13970, 4-hydroxyproline epimerase.	2.34726e-133
NZ_CP017172.1\|WP_140795179.1\|7906784_7907642_-\|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_CP017172.1\|WP_174259366.1\|7903127_7904801_+\|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_CP017172.1\|WP_140795169.1\|7892984_7894400_+\|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_CP017172.1\|WP_140795178.1\|7905600_7906764_+\|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_CP017172.1\|WP_140795170.1\|7894523_7895174_+\|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.	2.81365e-68
NZ_CP017172.1\|WP_140799897.1\|7884786_7886178_+\|ammonium-transporter	gnl\|CDD\|223083	COG0004, AmtB, Ammonia permease [Inorganic ion transport and metabolism].	5.21754e-156

>NZ_CP017172.1|WP_140877232.1|7895330_7897481_+|catalase
MKPRKPSAKTRPTTLKSESLEPHRMHAEGKVLTTDQGIPISDTDNSLKAGIRGPTLLEDFHFREKMMRFDHERIPERAVHARGAGAHGYFQVYKSLEKYTQARFLTDPSLRTPVFVRFSTVGGSRGSADTVRDVRGFATKFYTEEGNFDLVGNNMPVFFIQDGIKFPDFVHAVKPEPHNEIPQASSAHDSLWDFVSLVPETTHMIMWLMSDRAIPRSFRMMEGFGVHTFRLVNAAGKATLVKFHWKPLLGNHALAWDEAQKLSGKDPDFHRRDLWESIEKGDFAEYELGLQFIPEGDELKYGFDLLDATKLLPEELVPVQRVGKLTLNRNPDNFFAETEQVAFCVANVVPGIDFTNDPLMQARLFSYLDTQLTRLGGPNFAELPINKPVCPVTNHQQDGFGRQTIPTSRANYHPNSLGGDCPVLANPTNAFRHYQERVEGHKIRARSGSFSDHFSQATLFYKSLSKPEQEHLVAALEFEIGKVERVEIRERVVNQILVNVDPELAVRVARAVGVTPPKVSKPPKPSKAAGKKAAPSVETSPALSMENSPHDSIRTRKIAALVSDGFAGKELDGVRKVLEERGATLELVGPTLSPVTSQEGREERPLRTFSTASSVMYDAVYVPGGEKSVAALRRVPLAVDFVREAYVHCKALALSADADTLLDAAGVRDLEAPPSKGLDATRGVVRSAKMETKGFGQLFAESIARRHWEREAPPPA
>NZ_CP017172.1|WP_140795170.1|7894523_7895174_+|SRPBCC-family-protein
MLKKILVGLAAVILLFVGFVVTRPDTFTYQRAAVLPVSADIAFALVNDFHRWTEWSPWDGLDPQAQRTYSGAESGTGAGYAWVGNDQVGEGRMTITDSKANEQVTIKLEFIKPFAATNTSTFAFSAAEGGTQVVWAMSGENNFVSKAMSLFMDMDAMIGKDFEKGLATMKDVAVADAKKHAEAEAARIAEEKARTEAAAAAPAGEGAPAVAAPAVP
>NZ_CP017172.1|WP_140795169.1|7892984_7894400_+|L-serine-ammonia-lyase
MAVSVFDLFKIGIGPSSSHTVGPMRAARMFARKLADTGVLERLTRLKVELFGSLGATGKGHGSDKALVLGLMGETPEGVDVEAVPAIISRWRAEGRVALLGQREVTFRDGEHLVMHRRRSLPFHPNGMRFTACGGDGAELASAVYYSVGGGFIVDESAAVAGKDPLSKDTTPLPFPFQSAAALLAHCERERMSFSSLMLANEKTWRDEAEIRAGLLRIWDVMQACVRRGCTSGGILPGGLKVERRAAGMYQKLISRPEAGLTNPLTVLDWVNLYALAVNEENAAGGRVVTAPTNGAAGIIPAVLHYYWRFVPGANEDGVVRFLLTAGAIGVLYKENASISGAEVGCQGEVGSACSMAAGALTEVMGGTPLQVENAAEIAMEHNLGLTCDPIGGLVQVPCIERNAMASVKAINATRMALSGDGRHFVSLDKVIRTMRDTGRDMKDKYKETSRGGLAANVLEVANLSVGLPEC
>NZ_CP017172.1|WP_140877230.1|7890884_7892393_-|tail-fiber-domain-containing-protein
MAASTAHGGGRCSVNARASRNPPSGVWTFPRRKSVGVVSYPDSTPGDEMRGRGLFAAMSCITLATTGCGSEGPPAQNWEVGSGLRLDDSNVVSVAYGTGPGTVVEGSDPRLRDARPPLPGSGGYIQNGTQPQDASLSLAGTASTRSGLFVDAAAAVSSPVPLLRVTNTSEAQPVWDALPVFTVDSGGGLLARGAYELGAPLPMSGRGMRLMWAPARGVFRAGNAETEWDIANVGEYSWAGGNRSRASGYGTFAFGDQCVASGTVAVCFGSSNQATGTASFTSGASNTASGFGSTALGYTSTAAGQGSVALGYSAQATGDYGVALGYRVSTGGRTGAFIWGDGSTTTATSTADNQFMVRAAGGVRLRTRADLGTGCDLPANSGVFTCTSDRNMKEDFRHVDGEALLAKVAKLPVESWRYKGEDRQVRHLGPVAQDFRAAFGLGTDDTSIGMLDIDGVNMAAIQALERRTRELNAKSAELDALKAELAELKASVAQLKASLPRP
>NZ_CP017172.1|WP_140795166.1|7889981_7890806_+|hypothetical-protein
MRFQRFAFAAMSFACTAAMAAEPIQPPWGKESNLGEKMMLEATSVCTDGKGHFVALTPDDEDTNAVLYYGDEKQFVQVPRPGPYTSATSFLDPRFFNKGANPNFRGIDWRVMSSVEIDRKERTCSLTCGEKKIPLTMLDGEPASELLRKASFQPNPQKFVPYALLRDTKGAYYFVDRGFHEAEKKSYRVFIGPRGSLKAQKMTNVISDSEGEIFSTKRGDLRLLLDKAKPALWIENTKRRLELRQVPVDENLPLIYNELGVYEGARLGTPCDDQ
>NZ_CP017172.1|WP_140795165.1|7889016_7889967_+|hypothetical-protein
MRSASGPRSRQRSVPRSRSSARSTTSSSETAGHPGRGALMQHEVIRLRNMVAVIVAAVALGASQALAAAPVEAGKVYSGTEGEEVAVVPLTPRSDKKFILRVKGTGSEFDGLVFPYEQNDWSTRSTEQFNYSTQWHGRKYTALHVRDTKYELYVPGRQRPIRLAYDEKKTAALKPEEVYAQHQKQMKDGSLAKLMAFDRKGEESGHEKEFAATLQEMNNACGTSVAARIDWSSINEDQLKELSISSFCGTPLTSLKELCTASAIAKQTIQEKVKQVSCRFGSALEPKIEADRVIWTTSRDASNQDKFATKYFKQNL
>NZ_CP017172.1|WP_140795164.1|7887098_7889102_+|protein-kinase
MTLPADGDLRIDEVLRNTYRIVSLLGRGGMGSVYLAQHLRLPGKQVAVKVLRGGDHLTPEIFARFRREAEIASRLGHPNIVEVLDYDTLENGNPFLVLEYLRGESLQERLERGRLPMEDVVSFTRQMGSALQAAHGAGVIHRDLKPANVFLVPTDSGGVVGERVKLLDFGISKVLSSTTVQTQEATIIGTPQYMSPEQAQGKNRDIDARTDVFALGCIVYEMMAGKPVFGSGSLAQMIFRVVYEPPEPLAPLCPEATPEAISAVMRALAKSVDERYPDVSTFIADLTGTPLHSLSTTAGNQPAPRPQAPTSGIALPSAGPASLSATVPPGSLKVAPDTGREGFDSTMAPGTGQQGFSPSATGQMGVAQAQGFSPSATGQMGVAQLSAASLIDPPGLEPTLISKQLPAIPVQERPAQHHTAVSVPVPIPSAAEAHAAAALLSAPSTPVSSPPAAKGRGAIIGATAAVLLASSMGLVWWMKGGTSGSGSPTTPVTDTRVPQDAQPANGTQQANGTQQANGTQQANGTQQANGTQANDTEQANGTQQANGTQTPPDTDNPQQVVVTTNTVPDKPTSRPVTRPEAKEELPEQVRKLLKDGESALASGDASRAIALARSSQRTKRSMAAYSLLTRAYCQQKDLGGAVSEWPKVASAERAKVKKFCQKHDIEL
>NZ_CP017172.1|WP_140795163.1|7886252_7886936_-|GNAT-family-N-acetyltransferase
MPKAKTPKPPDSLEVRVRRIHRRDLNRTWEFLKLVFRDVNRETVEYQRPRSKRRFLEVYTSEWIEQLLYEVDGSIVGYSECAFEATGDDNWVNPRWFEKRGMRPLFVEELAVHPDYQGRGVGSFMLDQLQHLARTRGCTHLVLEVAENNESALTWYRTRSFYKLDAAIFMAQKVPGEPDLLPPRRLKRRQKPTAEAGTPSTGPMPETAPTRAATRKARAPAARKKSS
>NZ_CP017172.1|WP_140799897.1|7884786_7886178_+|ammonium-transporter
MKKWFAMALLVGVGVAGLLVEPAAQLKQGGPINTADTAWILTATALVLLMTPGLSFFYGGMVRLKNVVSTLLQSFIAMAVISLIWVMVGFSLCFGDSFHGLIGDPRTFFMFSGVGGETHPDLAPTIPLMLFALFQLKFAIITPALITGAFAERVRFKAYVLFMVLFTLVIYAPLAHWTWHPEGFLRQWGVLDFAGGTVVHMSAGFAALAGALVLGRRKVHVENTTHAPANIPFVMLGTGMLWFGWFGFNAGSAMSASSLATLAFATTNTASAAAMLGWIAFDWLRGRKPSAMGACIGAVVGLVAVTPAAGFITVGQSIVVGLVASFVSNAAVHFKNRTSVDDTLDVFPCHGLGGVVGMVLTGVLAKDVGLIHGETRTFMMHMLALVLVSVFSFAGSFLLYKLVDRIVPLRVTREHEEEGLDLSQHGETVGESIIAPGPQSALTATTAVATEPASDASSLPQPA
>NZ_CP017172.1|WP_140795161.1|7884358_7884643_+|hypothetical-protein
MKTKLAAVTLVASLLASSAAWAAVTVRYYNRDSRDHSWSVVCSGVKTSVTFGKSQTASVTIQGSGPCSVKTDAGTVVLKGGEDLEIKDGRIQVK
>NZ_CP017172.1|WP_140795173.1|7898664_7900377_-|sodium:solute-symporter
MTGLDWVVLGGTIAFIVVWGIWKSRGAASSEEYLRGGRELKWPTIGLAVMATQASAITFLSVPGQAYEDGMRFVQFYFGLPIAMIIISAVFVPIYYRLNVITAYEYLESRFDLKTRLLGAFLFLIQRGLAAGITIYAPAIILSAILGWPLEPTVIVMGAVVILYTVTGGAKAVSQTQKQQMVVMMGGMVVAAIVIVWRLPEHVSFGKAVDVAGAFGRMNVVSFDFDMQDRYNFWSGITGGLFLSLSYFGTDQSQVGRYLSGRSISESRLGLLFNGVLKIPMQFLILFVGILVFAFYQFSTPPLLFNEALRTRVQGTAQAAEYAALESKWEQVQSGKRAEVERYLSAVDSGDVAAGDASRALLQGHAQEASAVRKEAKDLVVRALPGAETKDSDYIFISFVKRWLPSGLFGLLIAVILSAAMSSIASELTALGTTTTVDFYRRVFQRNASDRHVLVASKLFTVFWGVVAVGFATFASLLDNLIQAVNILGSIFYGTVLGIFLVAFFVKHVRGHAVFAAAVISQATVIALFFLSDVGYLWFNVIGCALVVVLGLVMQAVLPRGETPAPATGA
>NZ_CP017172.1|WP_140795174.1|7900373_7900553_-|hypothetical-protein
MSTAPHLNPSEPSAEAPAPRPELDDAPPLLGSWRNIYILVLGTFVLFLALGWVLTEVYS
>NZ_CP017172.1|WP_140877236.1|7900549_7903033_-|PIG-L-family-deacetylase
MRNLLLGMTLAMSLGIGSTAVAQPPRQLHAGEIAAGLKRLGVTGSVLYVAAHPDDENTRLLAWLVGDRGLRAGYLSVTRGDGGQNLIGTEQDALLGLIRTHELLAARSVDGAEQFFTRARDFGYSKSAEEALRIWGHEAVLADVVLAIRRFQPDVIITRFTTEPPNHGHHTASALLAAEAFIAAADPKRFPEQLSEVKPWKTDRLLQNASHWWFKPDEDLSRYVKLEVGGYDALLGRSWGEVAAESRSQHKSQGFGQATDRGPSTEYFTPLAGTLPKRDVFEGLDFSWKRWKGSEAVSRAVAAATKAFDARAPHRSLPALVRVHEALTALPDTHPWKAPKLRETEALIAACAGLFLEVRASAPTGIPGLPVALDVVALNRSPAAVEWVGLTLPGEKPEAVGKALGANVPLKLSRTVTLPTTAPISTPYWLREPVTGGLYTLEGEDRALTGQPEGVPALSVAFEYKVAGRRFRAVRPVVYVWTDPVSGELYRDFEVVPPVTATLAQDVLMFPNGESRVVPVVLVAGMDQVPGTVRMVAPPGWRVEPASVEFKLATRGDERTITFQVTPPQGSTQKGDLSVDVDVRDRAWSWRARSVSYPHIPPLTVRQPSTATVVPFSLAMKGKRIGYIPGPGDRVAESLSAVGYEVTLLPEERLAREKLERFDAILVGVRAFNANTHLTVHRERLLQYVEGGGRLVVQYNTNSRVGPLTSFVGPYPLEIGRDRVTDETAVMTPLRADEPLLRTPNALTAADFEGWVQERGLYFASSWDARYQPVFAMHDAGEAPLQGALLVARHGKGTFVYTGLAFFRQLPAGVPGAYRLLANILSQ
>NZ_CP017172.1|WP_174259366.1|7903127_7904801_+|bacillithiol-biosynthesis-cysteine-adding-enzyme-BshC
MHFRWRVRRDLLSRHAVTSSFSTAWLRGDASALSFLSDDYRHREARARAVAAAASRTVSPALLDVLGAQNARLAPSPARERNLALLAQPGTVAVVTGQQMGLFLGPLYTLYKAASAIVTARALREETSRPCVPVFWLQTEDHDLPEIDHCVIPRPGGGPCRLALELPDAAASRAPIAHRHLGPSVLPALATLRAELEAEPHAEEFLSLLERAYRPEATLAGAFTDVLSSLFADEGLVFVDPRDARLAPLAAPVHRFALQEAGALASVLAARTEALTRAGYTVQVHVRPGSPLSFFSPDALDGPRYRLDPAEAGAWSLVGHPDSSAITQDALHAALEREPLRFTTSALLRPLLQDTWLPTAAYVGGPGELAYFAQLAPLYAHAGRPMPLAIPRARFRVLDDRARRWLGRVGLQPDEVNVPRDTLLTRLATRDAPESLETPEALEARLFGAFSSELERVAGQVSAVDTNLQDALRRTEGTVRVAVSRLTGRYRRALARRDATAAEQVDRLRTFLFPEGAPQERVLGLPYFACRIGARAFTQLVLDACVPFSGDSKDLTP
>NZ_CP017172.1|WP_140877240.1|7904797_7905604_+|bacillithiol-biosynthesis-deacetylase-BshB1
MSANGTAYGIDVLAFGPHPDDVELFCGGLLASMAARGYRTGIVDLTRGEKSSRGTLQSRAEETEAATRALGLAHRENLELPDGWLNPWAGFDTPEPERARTAAVARVVEALRRLRPELVVVPWEQERHPDHEAASALVTRALFFAGVRKFDAEPAAEPFTPRQVLYYPLRHLAEPSVVVDVSAVYERKLAAVHCYASQVMPRPDAPPTLVGSPLSLSSLEARDRFYGAQIGVTHGEPYVLREALGLADLLDHFRRNSFARPLFFPART
>NZ_CP017172.1|WP_140795178.1|7905600_7906764_+|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA
MNAPLNVAITCFPTFGGSGMVATEIGLAMADRGHRVHFIARDLPVRLHGANRKVVFHEVTESDYPALQQSSTYPIALASKMIEVANYERLDILHVHYAVPHATAAWMAREVLGHKAPRVVTTLHGTDTTLVGIDPSYLPITRFSITRSDAVTVPSAYLRRATWRGFDIPESVPIDVITNFVDTARYAPVRDRACLRALFPALRDHEPVLIHVSNFRPVKRIVDVVAIFTEVHRHRPCRLVMVGDGPERSPAERMLREMGLEGRVAFLGKQDRFEELVAASDVFLLPSEQESFGLAALEALSCGIPVVASDLGGIPELVTHGETGFLAPLGDVPAMARHVLTLVEDAERWQGFSHRARAQVLERFQKEPAIDRYEALYRRLLTGPLRR
>NZ_CP017172.1|WP_140795179.1|7906784_7907642_-|DUF2911-domain-containing-protein
MRTMKNQLLSCMASALMTLSAMPALAQLKLPAASPAAKVTQEVGVSEISVEYSSPAVKGRKVWGELVPNDKAWRSGANSATKITFSHPVTFGGKAVPAGSYAIVSLPSQKGWKVMLNTDLGLWRGGAPYDTAKDVASVSATTTEIPSRERLTYLFTDTTDTGTRLDLEWEKLRISVPITVDTAALAKANIEQAQKSTAMMHASAASYVAEATKDYAAALNHADAAVAANPTWYNHWVRAGVLSQMGKYSEARKAAQAAWDLGQKDKNFFYRDQVSKALAEWKNKK
>NZ_CP017172.1|WP_174258951.1|7907860_7909153_+|AAA-family-ATPase
MKLTRLEVHHYRNVVPGTSLVFSPSCNLVLGENGTGRTTLLELISTVLGSDFSGLIHEPFALEYDLAFPGMKLHVFVRNEENAPAPDAEAPPRKGSALMPLRTPALDSSLHPRIEVDVQFHSPSARLVMRADAAGMDCKVDGEAVWSRSMHWSLLDRSVWTLLFMTAQYIDAGMKERLKELLRRTFLLAPQRFDEALGMFERIGAIRYAMEVRDGEVFPLGLMALPTWMPGWLREQMEQPSVTDVLELTHDAREGSFLAKFVALAGFEAGRFRVEVLEKRSFENGGRVGFGGFGFEFTRRDGRVLTHEALGFGQKRLLSLLYYLDVNEDFAIADELGNGLHPRWVEASMREMGARQVFLTSQNPLLFEHTLFPSAEALRASLLLCGNTREDGPERIAWKNPTHEVAGRLFDAHGLGAHPLAELLRQQGLW
>NZ_CP017172.1|WP_140877243.1|7909408_7910344_+|proline-racemase-family-protein
MRRIRVIDSHTGGEPTRVVTDGGPELGAGDLASLRERFREKFDAFRKAIVCEPRGSDVMVGALLCPPVNASSVAGIIFFNNVGYLGMCGHGTIGVVKTLEYLGRIGPGVHSLETPVGVVKATLHPDGRVSIANVPSYRWAHDVAVSVPGHGEVRGDIAWGGNWFFLSRATHLPLELSRTPALLAYTSAIKQALSDQGITGEGGAEIDHVELYAPSPTPGVDARNFVLCPGLAYDRSPCGTGTSAKVACLAAEGVLAEGATWVQESILGSRFEARYVRDGARILPTITGTASVNAEATLLVEPTDPFAWGIG
>NZ_CP017172.1|WP_140877245.1|7910340_7911477_+|FAD-dependent-oxidoreductase
MSAFDCVIVGGGIVGAALADVLSADGVSVALVEARSIGAETTACGMGHLVAMDDNAAELALTSWSVSLWRELADGLPRAVEYDACGTLWLAADDEEMAAVSAKVANYRAAGVRAEVLDSAALHEAEPALAPGLVGALRVVDDAVLYPPLAARTFALRARARGARLMTGCPVRELRSGSVVLSNGEVLTARHIVLAAGVASPALCPGLPISPRKGHLLITRRGAPVVHHQLVELGYLKSAHGTDSASVAFNAQPRVTGQLLLGSSRQPGDATREVDAALLERMLKRAAMFLPGLDGLQALRVWTGLRPATPDGLPLLGPHPEKPWLWLACGHEGLGITTATGSARLVADQLLGRTSPIDARPYSPARFLAVSSREVAHA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_18

8119900-8119974

Orphan

Consensus_repeat	Method
CGGGGACGGAACGTTCCTTCCAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP017172_18

>merge|NZ_CP017172|18|8119900-8119974|CRISPRCasFinder
CGGGGACGGAACGTTCCTTCCACGCACCAGGCTCGTCCCCGGGCAGGGGCCGCGTGGACGGAACGTTCCTTCCAC

>NZ_CP017172|18|17|8119900-8119974|CRISPRCasFinder
CGGGGACGGAACGTTCCTTCCAC	GCACCAGGCTCGTCCCCGGGCAGGGGCCG
CGTGGACGGAACGTTCCTTCCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140857216.1\|8130437_8131013_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140877356.1\|8108615_8109968_-\|IS1182-family-transposase	unknown	unknown	gnl\|CDD\|226192
NZ_CP017172.1\|WP_140877372.1\|8125354_8128564_+\|type-2-lantipeptide-synthetase-LanM	unknown	unknown	gnl\|CDD\|274840
NZ_CP017172.1\|WP_140877366.1\|8119359_8119893_+\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238017
NZ_CP017172.1\|WP_140877378.1\|8131331_8132567_-\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|226587
NZ_CP017172.1\|WP_140799987.1\|8106342_8107074_+\|transglycosylase-SLT-domain-containing-protein	unknown	unknown	gnl\|CDD\|381594
NZ_CP017172.1\|WP_140795318.1\|8113934_8114972_+\|ATP-dependent-6-phosphofructokinase	unknown	unknown	gnl\|CDD\|235111
NZ_CP017172.1\|WP_140877374.1\|8128651_8128894_+\|mersacidin/lichenicidin-family-type-2-lantibiotic	unknown	unknown	gnl\|CDD\|274841
NZ_CP017172.1\|WP_140877368.1\|8120261_8121488_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP017172.1\|WP_140795323.1\|8121441_8122113_-\|class-II-aldolase/adducin-family-protein	unknown	unknown	gnl\|CDD\|181226
NZ_CP017172.1\|WP_140877352.1\|8107089_8107818_-\|glucosamine-6-phosphate-deaminase	unknown	unknown	gnl\|CDD\|238693
NZ_CP017172.1\|WP_140877362.1\|8115063_8116707_+\|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl\|CDD\|341284
NZ_CP017172.1\|WP_140877364.1\|8117100_8119161_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140857208.1\|8122109_8123216_-\|S-methyl-5-thioribose-1-phosphate-isomerase	unknown	unknown	gnl\|CDD\|235578
NZ_CP017172.1\|WP_140795315.1\|8105603_8106332_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP017172.1\|WP_140877370.1\|8123212_8124097_-\|S-methyl-5'-thioadenosine-phosphorylase	unknown	unknown	gnl\|CDD\|181584
NZ_CP017172.1\|WP_140795314.1\|8104944_8105505_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377224
NZ_CP017172.1\|WP_140795326.1\|8124348_8125158_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223999
NZ_CP017172.1\|WP_140877376.1\|8129085_8130423_+\|AHH-domain-containing-protein	unknown	unknown	gnl\|CDD\|379603
NZ_CP017172.1\|WP_161607142.1\|8111091_8111970_-\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	unknown	unknown	gnl\|CDD\|378065

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140877356.1\|8108615_8109968_-\|IS1182-family-transposase	gnl\|CDD\|226192	COG3666, COG3666, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	8.62159e-20
NZ_CP017172.1\|WP_140877372.1\|8125354_8128564_+\|type-2-lantipeptide-synthetase-LanM	gnl\|CDD\|274840	TIGR03897, Lantibiotic_mersacidin_modifying_enzyme, type 2 lantibiotic biosynthesis protein LanM. Members of this family are known generally as LanM, a multifunctional enzyme of lantibiotic biosynthesis. This catalysis by LanM distinguishes the type 2 lantibiotics, such as mersacidin, cinnamycin, and lichenicidin, from LanBC-produced type 1 lantibiotics such as nisin and subtilin. The N-terminal domain contains regions associated with Ser and Thr dehydration. The C-terminal region contains a pfam05147 domain, which catalyzes the formation of the lanthionine bridge. [Cellular processes, Toxin production and resistance].	0
NZ_CP017172.1\|WP_140877366.1\|8119359_8119893_+\|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).	1.81003e-18
NZ_CP017172.1\|WP_140877378.1\|8131331_8132567_-\|DUF1501-domain-containing-protein	gnl\|CDD\|226587	COG4102, COG4102, Uncharacterized protein conserved in bacteria [Function unknown].	8.63106e-67
NZ_CP017172.1\|WP_140799987.1\|8106342_8107074_+\|transglycosylase-SLT-domain-containing-protein	gnl\|CDD\|381594	cd00254, LT-like, lytic transglycosylase(LT)-like domain. Members include the soluble and insoluble membrane-bound LTs in bacteria and LTs in bacteriophage lambda. LTs catalyze the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), as do "goose-type" lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue.	2.75421e-35
NZ_CP017172.1\|WP_140795318.1\|8113934_8114972_+\|ATP-dependent-6-phosphofructokinase	gnl\|CDD\|235111	PRK03202, PRK03202, ATP-dependent 6-phosphofructokinase.	1.76696e-161
NZ_CP017172.1\|WP_140877374.1\|8128651_8128894_+\|mersacidin/lichenicidin-family-type-2-lantibiotic	gnl\|CDD\|274841	TIGR03898, hypothetical_protein_SrosN15_20203, type 2 lantibiotic, mersacidin/lichenicidin family. This model recognizes a number of type 2 lantibiotic-type bacteriocins, including mersacidin and lichenicidin. Members often are found as gene pairs encoding two-chain bacteriocins. Maturation is accomplished, at least in part, by a LanM-type enzyme (TIGR03897). This model describes only the leader peptide region. [Cellular processes, Toxin production and resistance].	7.7712e-18
NZ_CP017172.1\|WP_140877368.1\|8120261_8121488_+\|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.	2.40724e-48
NZ_CP017172.1\|WP_140795323.1\|8121441_8122113_-\|class-II-aldolase/adducin-family-protein	gnl\|CDD\|181226	PRK08087, PRK08087, L-fuculose-phosphate aldolase.	1.30414e-81
NZ_CP017172.1\|WP_140877352.1\|8107089_8107818_-\|glucosamine-6-phosphate-deaminase	gnl\|CDD\|238693	cd01399, GlcN6P_deaminase, GlcN6P_deaminase: Glucosamine-6-phosphate (GlcN6P) deaminase subfamily; GlcN6P deaminase catalyzes the reversible conversion of GlcN6P to D-fructose-6-phosphate (Fru6P) and ammonium. The reaction is an aldo-keto isomerization coupled with an amination or deamination. It is the last step of the metabolic pathway of N-acetyl-D-glucosamine-6-phosphate (GlcNAc6P). GlcN6P deaminase is a hexameric enzyme that is allosterically activated by GlcNAc6P.	2.65858e-115
NZ_CP017172.1\|WP_140877362.1\|8115063_8116707_+\|long-chain-fatty-acid--CoA-ligase	gnl\|CDD\|341284	cd12119, ttLC_FACS_AlkK_like, Fatty acyl-CoA synthetases similar to LC-FACS from Thermus thermophiles. This family includes fatty acyl-CoA synthetases that can activate medium-chain to long-chain fatty acids. They catalyze the ATP-dependent acylation of fatty acids in a two-step reaction. The carboxylate substrate first reacts with ATP to form an acyl-adenylate intermediate, which then reacts with CoA to produce an acyl-CoA ester. The fatty acyl-CoA synthetases are responsible for fatty acid degradation as well as physiological regulation of cellular functions via the production of fatty acyl-CoA esters. The fatty acyl-CoA synthetase from Thermus thermophiles in this family catalyzes the long-chain fatty acid, myristoyl acid, while another member in this family, the AlkK protein identified from Pseudomonas oleovorans, targets medium chain fatty acids. This family also includes uncharacterized FACS proteins.	0
NZ_CP017172.1\|WP_140857208.1\|8122109_8123216_-\|S-methyl-5-thioribose-1-phosphate-isomerase	gnl\|CDD\|235578	PRK05720, mtnA, methylthioribose-1-phosphate isomerase; Reviewed.	0
NZ_CP017172.1\|WP_140795315.1\|8105603_8106332_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	4.15299e-12
NZ_CP017172.1\|WP_140877370.1\|8123212_8124097_-\|S-methyl-5'-thioadenosine-phosphorylase	gnl\|CDD\|181584	PRK08931, PRK08931, S-methyl-5'-thioadenosine phosphorylase.	0
NZ_CP017172.1\|WP_140795314.1\|8104944_8105505_-\|hypothetical-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.	0.00826159
NZ_CP017172.1\|WP_140795326.1\|8124348_8125158_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|223999	COG1073, COG1073, Hydrolases of the alpha/beta superfamily [General function prediction only].	3.03448e-09
NZ_CP017172.1\|WP_140877376.1\|8129085_8130423_+\|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.	1.00689e-24
NZ_CP017172.1\|WP_161607142.1\|8111091_8111970_-\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	gnl\|CDD\|378065	pfam08843, AbiEii, Nucleotidyl transferase AbiEii toxin, Type IV TA system. This family was recently identified as belonging to the nucleotidyltransferase superfamily. AbiEii is the cognate toxin of the type IV toxin-antitoxin 'innate immunity' bacterial abortive infection (Abi) system that protects bacteria from the spread of a phage infection. The Abi system is activated upon infection with phage to abort the cell thus preventing the spread of phage through viral replication. There are some 20 or more Abis, and they are predominantly plasmid-encoded lactococcal systems. TA, toxin-antitoxin, systems on plasmids function by killing cells that lose the plasmid upon division. AbiE phage resistance systems function as novel Type IV TAs and are widespread in bacteria and archaea. The cognate antitoxin is pfam13338.	1.62428e-10

>NZ_CP017172.1|WP_140877366.1|8119359_8119893_+|FHA-domain-containing-protein
MPSVKQLRPFALATLEAFLEASGRVVLVQQPPEPVFQQVAMRLGEARTVGMAHRTRLVDRLFVMLRGFDALEVHFLRPETEGEELSVGRIEGCSLVVPDPSVSKNHATLRWHAQAGDCSVRDLGSMNGTWVNASALGPDQERMLNDGDALAFGDAQFLYLRTETLHAHLRMASPSRD
>NZ_CP017172.1|WP_140877364.1|8117100_8119161_-|hypothetical-protein
MMMRMKRYGAGLLTAGLLAVAPACGDSDEGAPPDAGLPDAGRPDAGDSGIPDAGDSGTPDAGEELPPLMVPAGCNPLASEHDCLLPYPSDYFLEEDAALPSGHRVRLSEAAKLKAPDGAAFDFTDLHPADGYSHGTQVLALFPDGVDDARLPSVTSPTAATNGNTVFLDAERGEGVLHFAELDPRASDDARRALLLRPVVRLRNTARYIIALRGLTAEDGTPVPVPEGFRRIRDGQTAGDPLLAPLAARYEADIFPALEAAGVPRAELQLAWDFTTESQEGVTRDMLQVRRLAMEALEATPPAVTVTDVRDDVDANVARRITGTLRVPLFLESDQPGALLARDEEGRVRRNGDAEVPFTLQIPHSVWGQSVAPVRFLQYGHGFFGRQAEADGSFVRPFIQATRMVVLTVDWWGMSQTDAPGVLQAMAGNPGQTMRFTDRVHQGMVNQLAVTYAARTTLGALTELQDDGVRVFDPEQTYFYGISQGHILGGTYVALSPHVSRAVFSVGGADFSLMMFRARPFGMFLDAIAQTVPDALDQQKFAALTQTSFDRIDPLTYAPHVLGDLYPGAPASRRVLVQYGLGDAQVPNVATELHARAMGLTQQLPSTWRVPMLPAEEGTVEGSALVQFDFGLPPPLPGTVADLPAADNAVHEGVRRDDDGREQVDRFLRPGGQVEVTCDGICLGGN
>NZ_CP017172.1|WP_140877362.1|8115063_8116707_+|long-chain-fatty-acid--CoA-ligase
MLPGRMMDFPLTLSHLMERARTFYPRSEIVSRNPDKSLHRYTYADFYARTCRLANALTRLGVKAGDRVATLSWNHYRHLEVYYGVPCMGAVVHTLNLRLHPNDLGYIARHAEDSVVVVDRSLLPLFEKFKDAVPSIRHVIVVPDAGPAPEGTLDYEALLAAESPDFDFPQLDENSASMLCYTSGTTGNPKGVLYSHRSTVLHALACCMTDVTGMREADAVMPVVPMFHAAAWGLAFDAVLTGAKLVLPGPHLDPPSLLDLMAAEKVTMAGGVPTIWIGILALLDQSPARWDLSSMRSMLIGGSAAPPSLIEGFQQRHGLEVVHAWGMTEMSPVGTMAKVKGPLRQAAPETKSSARASQGFALPFVETRVASDDGTLLPWDGETMGELEVRGPWVASSYFSDEGEDRFTKDGWFKTGDVVTIDSQGYVRICDRSKDVIKSGGEWISSVALENALMAHPAVLEAAVFAGKHPKWDERPLAAVALKEGQQATKEELTAHLAGQFAKMWLPDDYVFVPQVPRTSTGKFLKTKLREDYGDHLLKNPKADAAT
>NZ_CP017172.1|WP_140795318.1|8113934_8114972_+|ATP-dependent-6-phosphofructokinase
MKVAVLTGGGDCPGLNAVIRAVVRRANAHGFEMMGLRDGWKGLLEDNHFRLTRETTSGILHRGGTILGTSRVNPFKVENGLERVKRAIERNGIHAIIAIGGEGTLSAATRMSQEGLRIVGVPKTIDNDINATDFTFGFDTAVAIATEAIDRLHSTAESHKRVIVCEVMGRHVGWIATYAGIAGGADVILVPEIPADLAKVAEHIQRRHAGGRTFSIVVVAEGTRIKLSADQQEQLVTSGALDEAGRPRLGGVGTILAHEIERRTGFETRVSVLGHIQRGGAPTAHDRVLATRYGVHACDMVARGEFGKMAALRGNDIISVDLADATRELKRVPQEFFEVAQVFFG
>NZ_CP017172.1|WP_161607142.1|8111091_8111970_-|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein
MQRTGELVVSAIGSDDELYERLVLKGGNALQLIYKVGARASKDYDFSMQKDEDPEWLRKRLEKAVHSRFELEGYVVLDFRFAPRPQRQTEATRENPKWGGYNADFKFLSKDDWAAAVSTVRAKRSKRAKHEQLEEEELLEYRRNISQKVEVEISKHEYTEGKASAEVDGYPVYVYTLPMIAAEKLRAICQQMKEHGQRKNPAPRPRDFYDIHACVVYGKVDLAQSIPTLRSMFSVKDVPIELLAHIKDYRSFHANAWAQVESAVPGEQLQPFDYYFEFVLNEVGRLQAAGVI
>NZ_CP017172.1|WP_140877356.1|8108615_8109968_-|IS1182-family-transposase
MSKKFRPWNVQQDFLLPPSLLDWLPEHHLARFVLEVVEELDLGPIYESYEEELRGYPPYEPKMMVALLLYAYCSGVTSSRKIERKTQEDVAFRVLAANQSPDHSRISEFRRRHGAHFESLFVQMLKLCAKAGLVKLGHVALDGTKLKANASKHKAMSYERMQQEEEKLHEKVKELLAQAEAVDTQEDALHGKGKRGDELPEELRRTQTRLQRIREARQALEAEAKAAAEADKGKDDDDDAPPPAQDLPSHTVPHTAEGKPTPKAQRNFTDADSRIMKKGASFEQAYNAQAAVDAAHQVIVAQALTNQPPDAEHLSALVDRVAAHLEEVPGKLSADAGYFSAKNVHWLKSVGVEPYLATGRQKHGEAPPRVRGRPPSGLTPKERMARKLATKQGKEVYRMRKAIVEPVFGQIKEARGIRALLRRGLTAAREEWALICATHNLLKLFRATAA
>NZ_CP017172.1|WP_140877352.1|8107089_8107818_-|glucosamine-6-phosphate-deaminase
MRIRVFDSEREAAAACAQRIARAVTARPSLVLGLPTGRTPLNVYRELVELFTRGGLDWAQVRTFNLDEFLGVSADDAGSFRAYMERHLFQHVNLSPAHIQFLNGAVEDAEAECARYEARLAEAGGLDLVLLGLGSNGHLAFNEPADGLRARCHRTRLSRQTREANLMLFGDDPSRVPMEALTLGMASILQARQALLLAFGEAKAEAVRGMVEGPVSPRCPASFLQLHPDVEVWLDPAAARAL
>NZ_CP017172.1|WP_140799987.1|8106342_8107074_+|transglycosylase-SLT-domain-containing-protein
MGRKRAARREGMTVPGWAWWLPCVLAPVVLLNVAVAWFGNSFVSPLSFSFLEAKAGALRAYLAHRPSCLVEGHAPLEPVIDAAERRHRLPAGLLRALVQVESETRVHRISPAGAMGPGQLMPGTAAMLGVKDPFDPEPAIDGSARYLAQQLRRFGDVRLAVAAYNAGPGSVNGRVPRNGETEFYVPKVLAAWELTRPPPPRKAPPAVKPVAKPKPVAPARSRAPASAAKEPKKPAAPEANGRS
>NZ_CP017172.1|WP_140795315.1|8105603_8106332_+|TetR-family-transcriptional-regulator
MASRDGTRADDAQETGKPPARPGGRREAHRREREQALEDAALKLFLARGLDGVTIDDITQAAGVAKGTFYRYFDDKAALVDGLLEPVRRELLAGLETCGHALAEARNVEAMFDAYRAVAAVIASALLQYPGVVRLYLQESRGPAVGARTKVAELARLVARHAVDITQKAHTSGLLRPIRPAVSGLAVVGAVERLLLAVLSEEDIGNPLELPDALTTLVLDGLRLPPEVRPRRRKLDGGPKRP
>NZ_CP017172.1|WP_140795314.1|8104944_8105505_-|hypothetical-protein
MIGIPLGWVYSNFGEWVLHRSVLHGLGKNRKSFWSFHWHEHHQKSRRHDMVDDQYMRSLWSWSAQTKELMGLAVLALAHAPLLPVAPFFVGTVWACAANYYFVHRRAHLDPKWAREHLPWHYDHHMGKDQNANWCVTHPFFDLVLGTRREFLNVQPPASKQPAPVEQPVPVPVEARKRAVAASGLR
>NZ_CP017172.1|WP_140877368.1|8120261_8121488_+|metallophosphoesterase
MGRLLFLLVFNVGAWAVLRSLWPGLLRKWRLGVFALGTFLSLVAWLYSAVAGRHAQLPVGDAALRVFSVGWSVAIIMIVLTGAPFLLLRRWLDRPARKEPPLTAPEANPAPPVNMARRNLLTNAGRAVPLLAAGTSSVGIANGYTQFSVREVDIHLPGLPPAMDGFRIGQITDVHVGTFIDTQYLQDAVRAMNDAKVDLQVMTGDLIDDLDQLDGTMAALSECKARHGMLAILGNHEHWRGLGAIRQAYADVEARGGPVRLLVDTSHAFEHAGQRVRVVGVDYPMSGRSHRVKAERMQQSAEAGFRDVAPEEVVLCLTHHPDFFPLAAERGARLTLAGHTHGGQVAFLGVPAFWFAFKYMLGRYRQGDHQLYVSGGTGHWLPFRIGVPTEVTVLTLRATGASAAGRTS
>NZ_CP017172.1|WP_140795323.1|8121441_8122113_-|class-II-aldolase/adducin-family-protein
MSGACEHLALRESMIATARRMNASALNQGTSGNLSVRVEAGFLLTPTGMDYDSLVPEDLVLMRFDGSHEGRRSPSSEWQLHRDILAARPEVGAVLHAHSMFCTTLACLHRDIPAFHYMVSAAGGTDVRCAPYATFGTAELAAHVLAALEGRKACLMANHGMVAVGRDLPAAFKLAVEVETLAAMYWRALQVGEPVLLDGAEMARVLEKFKTYGQQPTPPSREG
>NZ_CP017172.1|WP_140857208.1|8122109_8123216_-|S-methyl-5-thioribose-1-phosphate-isomerase
MKVHGKPMRSIWLAPDAQAAEAIDQTRLPHALVTVRLTTLDEAAHAIRSMQVRGAPLIGATAAYGVWLALRADASDGALEHALAVLRGTRPTAVNLHWALDDMRQLLAPLPPAERVAAALRRAEAISDEDVAINRAIGAHGLKILEDAWARKGRQGRLEVLTHCNAGWLATVDFGTALSPIYQAHEAGIPVHVWVDETRPRNQGAQLTAWELGQHGVPHTVIADNVGGHLMQHGQVDLCIVGTDRTTAQGDVANKIGTYLKALAAKDNGVPFYVALPSPTIDWTLRDGVREIPIEQRDGAELSDVTGRLASGEVATVRITPEGSPAANYAFDVTPARLVTALITERGVCPASHNGLLSLFPERRGRAE
>NZ_CP017172.1|WP_140877370.1|8123212_8124097_-|S-methyl-5'-thioadenosine-phosphorylase
MSNPTSPVIGIIGGSGLYQMDGLTDVEWKKVTSPFGEPSDELCFGTLGGHRVVFLPRHGRGHRLAPTDINFRANIDALKRSGVTDLLSLSAVGGLREEYPPGTFVVVDQFIDRTFARDKSFFGTGLVAHVSMAKPVCSRLGDAVISACEGLGVVARRGGTYLAMEGPQFSSIAESHLYRSWGCDVIGMTNMPEAKLAREAELCYATVAMVTDFDCWHPDHDAVTVDQVVSVLLGNAGKAKGLVKNVVPLLGAHTGHCAQGCHKALDHAIITAPTAWDAAMAEKLSAVAGRVLRR
>NZ_CP017172.1|WP_140795326.1|8124348_8125158_-|alpha/beta-fold-hydrolase
MLRLRRMLILILTTFGSIYLVLCVAVFALQRSLLYPAPKGTPPLAEGDGFSRLPLEGGLYVDLFHLPAPPGAPTVVHFHGNGEEVLTQIGLGNLMQARGLGFLTVEYPGYGASPGRPTEEGIYAAAEAALVWLRAKGVSAEQTVLSGRSLGTGVAVEMARRGHGSRVMLVSPYTSIPDIGATAFPFLPVRLLARDRYDTASKAAAVKLPVLIIHGEEDTLIPVDMGRRLGTLFPQAEVETVAGAGHNDVLEDPGKVYRHRMASFALGEP
>NZ_CP017172.1|WP_140877372.1|8125354_8128564_+|type-2-lantipeptide-synthetase-LanM
MGEGVTSRWVLGHALEERLPSLRMRGTPEAVDEARARRRLERWRKQEPLTRDSLWAQRLRASGLTEAELHTLLGEPAEALHARMGAPPPWQRVIEQAYTSEVSPPFSWPEPTPPGAALLGLVEPLVHEAHARLVSALDTCLRDMPAAPFEPERAARMLLAPLPRMLMPLLGRTLAVELRIAQLEGRLQGDTPEARFQDFAQHLRRRDVALDILARYPVLARQAVEYITAWEATGVELMQRLARDAAALWHRFHGGVPPGPLVEAQGGLSDPHQGGRTVFLLRFASGLRLVYKPRPLTAEAAFQQLLSWLNARGLTPPLRTVEVLSSDGYGWMEYVEAAPCQSAEEVRRFHLRQGALVALLYALDVTDIHYENLIAVGEHPVLVDLETLFHPHTLAASIRDVEKQPGAVLNGTVLKSGLLPQPAWRAKDGTEVDFSALGASEGQLTPLGYLVATAHGTDQLRFERRRMEIPGAANRPRLEGQDVSVAVQADALAQGFSTLYRLLAEHRDALLAPEGPLAAFEHAPVRVLFRGTASYDALLHESMHPHAMGDALDRQRFFDHLWLAVKERPYLAALIPFEQEELQRGDIPRFTALPGSKDLWSGAGRHLPGFFDDSGLERARRRLAELSPDDHERQLGLLRNALDRVRLAASPGARPRYPFHEPPEPAHPDTLLAAARRAGERLVALSFSGAGHSHWLSLERSDTEEWRLVQVGTDFYQGLSGIALVLAQLGALTGEARFTQAARGALRHLTWRLEAAPTQVRGVGILNGWGGILYALTHLGALWGERALFATAESFVDAMASRVEQDEHLDLGSGCAGALLGLLTLVGQHPSERASRLARVCGEKLLQTATPQSQGLGWLSPATGGQALCGLAHGGAGIALALLRLASVTGESRFHTTAMEALAYERGQFSPEAGDWPDLRADAGMHGGDGPAFMCGWCNGAPGIGLARISGLPLLDDHRVREEIAAAVRATLAGGLGYNHGLCHGDLGNVLFLLEAARALHDDTLLRRTYQLAGGILQGIESHGYQHGLPDSIETPGLMVGLAGIAHGLLRLAAPERVADVLSVAPPVS
>NZ_CP017172.1|WP_140877374.1|8128651_8128894_+|mersacidin/lichenicidin-family-type-2-lantibiotic
MSHSDKNHILRAWRDADYYDSLSDAERAALPASPASVMELEDATLAFITGGDAEASCPASPTPNELTCLYTNCGRIACCR
>NZ_CP017172.1|WP_140877376.1|8129085_8130423_+|AHH-domain-containing-protein
MTPRWAVPLLLLMIVTGCTTGRAVRLDTGPDTFVVTPREEPGSEVGAAELDDDEYEEAIAELARDVRPWRNPMQEARALFGVPSRGGVYRYEQHPLRLIPQRSEDADDPHLLESYADDELTRAYGQWCKRKDQPGDCLRLLDEGPLLASDGKYTLALAIAMDSVWDETAEALEGMTDPSAVMATITSAATMYLLLWALPEPISKGVAATLTAVAMAYLGVDTVWRLLDGWLTLVRTVEQATTFEQLSTAGETYGEVLGENAARVFVMLATAAIGNTAGLAAKSAGLPGSAQAAMAVETQAGIQYAAVGSVRSVALTAEGFTAALAPNAVAMASRGRGQRHHLATDKNEVSALRGGPWTPRFRDIFRKAGMELKDPENIVEIPGHKGPHTEQYHSFIHRRLLDALEDCRKVAECRKALTGELRLLAKEAQNRGTEVYRLLMKRPVG
>NZ_CP017172.1|WP_140857216.1|8130437_8131013_+|hypothetical-protein
MPKRSRYFWLDDEMKGGNWYLGDPVDKAGHEVEDIWEFIKGRPIRPAGCMTFPIREAGKRKDYSTAGVGRAPIVHFRVATIFAEMASNDVQLIPVDIEGCPDEYQVLVATKLIKCIDEKTSREILIWKPEDGRPEKVGKYRSVAGMRIDPTKVGDAKVFRTWGWTGALIVSEDIKAALERAKVTGAKFEEV
>NZ_CP017172.1|WP_140877378.1|8131331_8132567_-|DUF1501-domain-containing-protein
MTAPLTRRHLLRALGVTGAGLVCAPGFLGRALAASPASAARRTLVTVFLRGGVDGLSLVPPIEDAAYHRARPSLALRESGPDAALKLSGPFGLHPRLDALMPLWHDGRLAVLHGVGLPEPVRSHFDAQDFVESGTPGRKSTPDGWLNRALEEEEGAALRAVALQPTLPRALFGDAGALAMGRLEEFRLRGGRRGEEATRGFSALYAGAVDEALRTTGQGAFEAMALLDEDRLAKLPSRATVVYPKGPLGQRLRDIARLIHGEVGLEVAATESGGWDTHAAQGAATGAFANRCQELGGALAAFAADLGPRLEQVMVVVLTEFGRTVRENGSRGTDHGVGSAMLVLGGGVKGGRVYGRFDSLVPERLQDGRDVPAWTDVRAPLAEALRACRPGVELARVFPGFTPPPSLGLFG

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_19

8873473-8882729

TypeI

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

130 spacers

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

The CRISPR arrays of NZ_CP017172_19

>merge|NZ_CP017172|19|8873473-8882729|CRISPRCasFinder,CRT,PILER-CR,PILER-CR
CTTTCGACCCACGCTCCTCGCGTTCACGAGGAGCGACCGTACAGGCTGGACTCGTGGAAGGTGCCGTAAACGTTTCAACCTACGCTCCCCTCGTTCATGAGGAGCGACCCGAGAGGTTGTCCACAGCTCGGCCAACTACGGAGATGTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGACCATAGCCCCGGCCACGAGTCTTGCCCGACCCTGGCGTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGACCACGACGGATGCGCCTGCCCGCAGGCACGTGTGGTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGACCGACCAGGCCGAGTGGAACACGCGTGAGGCCGCGCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTGCGGAGGTTCGCCACCACCTCGCGGTGCACGTGGTTTCAACCCACGCTCCACGCGTTCACGAGGAGCGACCGCGCGCCGGGCGCACCTTCTGTTCTGTGCGTGGTTTCAACCCACTCTCCTCGCGTTCACGAGGAGCGACGCGACACCGGAGGACACAGGACGTGGCTCTGTTCGAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGGCCTGGACCATGGCTGCTCGCAGATGGTGCTCGGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACTGATGTTCTCTGCCATGAGTGATTCTCGAAACGGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGGCGCGGCCTTCCCGGCGCTGCCTGCGCTTGGGGTTTCAACCCACGTTCCTCGCGTTCACGAGGAGCGACGACGACAAATCTCCATGCTCAACAAGGCCCAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACACTACGCGGTGGTGCGCGGACGCGACGCGCACGGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGGCGCAGCTGCTCCACCATCACCCCCTCTACGTTGATGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACACCACCGGCCCGAGGAGCGGCTCGCACGAGAGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACCGAGGCGCCCACGCTCCCCACTGTTTGAAGAAGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCAACTTCAACGCCGGCAAAGGTCTACGCGGACTTTCTCCGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACGCCTCCGGGTCCGCGCGCTTCGCGTTGTGCGAGAGGTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGACTGGCGACGACTCTACTGCGCGCTACCACGAGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGGCCGGCGTCCTGGAGGGTGCCGCCTGGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCCGATGCCATGCTTGCGGCTCGGAGCGCCAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATCTCCAGGATGCAGCAGGCCTACCTCAACGCGTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGACCGGGCGCCTCTTTCGGTGGTAGGAGATAGACATGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGGCGGCCGTCGCGCAGGGGACTGGCGTCGGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCGGCTTGCGCTTCTTGGGCCGCATGCGTTGGAGGTTTCAACCCACGCTCCCCGCGTTCACGAAGAGCGACTGTCGTGGCACCACAGCAGCACCGGGTTCTTGATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCGCGAGAATCGGGCGGCACCGTCGAGTTGCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCGCTCCAAGAGGCCTCGGTACTGCTCAACGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGAGCGGCTTCGACGGTCAACTCGGTGCTTGCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGATGCCGTCCAAGTCACACCGGGCCGCGAGCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCGTCGTCGTCCAGCATCACGAGGGCCCTTTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGACATGACTAGGCGAGGAGGGCTTGGAAGCCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACTAGCTGCGCCGCTTTCCGGACCATTGCCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCGCACGGGCGAACTGGCGCTGTACGAGCCTCTTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGTTCCTGGCAGTCCGCGAGGACGCCATCATCCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCCGGGGCTCCGGGCCATGATCATGGGGGAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCGCGCAGTACCAAGTGGCCGTCGACTTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGGGATTCCCGCGCTCACGGGTGCAGGGCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATCGTAGGCGGCGCCCCCATCGCCCCCGAGAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCGCGACCTCGCGCGCTACATGGGCCTGGACTTCGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCAGCAGCTCCAGCTTGCCCCGCCACTGCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCTTCATGCCGCCACCCGGGCGGGCTCCAGCCGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCTCAATGAGGGCGCCGAGAATGGAGGGTGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACGAGCGCTCGGGTGCTGTCTAGCTTCTGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTCTGGGCGGTATCCGTGAAGTCCTTCACTCCGTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAGGTGTCGAGCTGTATCAGCGCGGAAATGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGGCACCCGTGAGGTCCTCGTCGCCTACCGGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTGATGCGCAGGTGGGCGCTCACCGCGTCGTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTCGGTGGGCACAAAGCACAAGAGCTTCAACGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGACGTCTGGACGACTCCGCCAAGCAAGGTGGTGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCCCCGCCGTCTACCGTCGCACCACCCAGGCCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTTCTGGCCGCCCACCTTCGTACGCTCGGCCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTTCCAAGCTGCAGCGACGTCTGCCGCGCTCAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACATTGTATGAACGACACGCCCCGCAGCTACTGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGTCACGTCGGCGGAGGCGCTGATGGCCAGGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCTGGAGCTGACGCTGGATGCCATGGCGGCGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCTCAGCCATGTGCTGCCTTCCGCACGGGAGAGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCGTCGCGGTGACGCCCAGGATGCGCGAGTTCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAATGAACGCGGAGCTGCGCCGGTGCGCCGCGAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCCCAGCACCACGACCGGCGGGCCAGCTCTCTTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGATGTACGCGCTCGCCTTCCTCTCGCGGGCTGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCTCGTCTCGTGGCTCAGGTGTCATCCACCAATCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACGTCCCCGTACGCGGCCCGGTCCGTCATCGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCCGAGGCAGCGCGAGGTGTTCGCCCGCCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGAGCCGAGCAGCGAGAACGTGACGCCCTCTCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGGGTCTGGTCGCTGTGGTGGATGCCCTGCTGGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACCCGCGCCCGCATCGCCCCGACGCCCACGCCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACGTCGTCCACCTGCTGGCCCATGCGGCGCTTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCTGCCGGCGGGCGCAGCTCCGGCGGAAGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAAACGGACGATGAGATGATTGAGCGGGCGCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGTAGCCCGCGCTATCCGCCACTGGCTCAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAAGCCGAAGGGCGCCGCATCCTCGCCCCCCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGACGCAACCGGGCTCGCGATTCGGCAGCTCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCCGGGCGGTCTCGGGTTCGCCACTGAGTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTGGAATCGATCCTGCCCATCACCGTCCCAAGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGAGCACAACCTGGTGGGCTCCTTCGTCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGATGCTCACCGTTGGCGCAATCCTCTCCTGCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCAAGTCCGGCCCTCGCAAGGGGCGGCCGAACGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCCGCATCTGGAGGGGCTGCCGGTGAAGGCGTGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGTGGTCCTCGATCGCGTTGTAGCGGATTGCGATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGCCGGCATTCTCGTACCCCTTCGTCGAGGCGGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGTACTGGCAGGCACGTCAGGCGGAGCTCGACTACCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGCACTGGGGGCTCTTCTTGGGCGTGGCCCTGGCGCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTGATGTGGGTCTTCCGCCAGTTCACCTTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGGTGGGGGCACGTACACGGGCAACGCCAGTTATGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGAGCAGACGCGGCTTTCTTCTGACGCGGACGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATGTCGAAGACGATGAAGTTACTGCGGATGTTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTCTCCAAGGTCCGTTTTCGCTGGCCGGAGGCGGAACTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGAGGACGGGCCATCCTGCGCGTCCTGCGATTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACAAGGCGCCCACGTGCCCTGCCTGCCGCTCTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGTGGGCGGCGTGTTGTCGACGAGGACGGTGCGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGGCGCTCAATCAGTTCACACGCTTCGGTGGAGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCATCGAGCTGGCGCGCGTGAACGACCACCTCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCGCGTCATCGCGTCCGCGGCCCAGTCCGCGAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCCGATGTGGAGTGTCCAGAGTGCGAGTCCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCTGAGTGATTACCGTCCGTGTTGCCACCTGCGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAATCCGGGCTTGAGCATCACCATAAATGGGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGAGCTCACAGGCATGACGTTGCCACGCAGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCGCCCGCGCGCACGTCACAGCGAGGGAGGACTCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGCCTCGTGCGGGTAGTGGGGGTGGATGACGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCCGCATCCGGTCAGCGCGCTTCGTGAGCACCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACACCGCGGACGGCAAGGTCTTCACCGCCGCGGTGGTGGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGGCTAGGGCTACGCCAGCCACTTGCACTGCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGCGCCGAGGGTCCCGGCCATGCCGCGAGCAGTAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCTGGCCACGGGCTGTCCCGTCGTGTTCCGGTAGGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCGCCGCGCTGCAACGCGTAGCGCCAAACTCCCTCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGCAGTCATCCACACCGCTGGGACGTTGGGCGAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCGTCCAATCGGCGACCCTCCACATCCTTGTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTGGCGGCCAAGGTTCCGACATCCGGGCGGAGGCGAAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACAGGGCGGGCGGGCAGTCGCGGACGTGGGTGCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCTTCACTGCGGCAACAACGCAGGGGATGCAGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTTCGTCAGCAGTTCCAACAGGGGGGAGGAGGTGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGGACGTCGTGCTTCTCAGCCCATTTCATCAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCCATTGCCGCCCACGTCTCCGCCACCCGTAGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCGCGGGGTGGGAGGCGAGGGCGGCATCACCCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGAGGCGCTCCAGGCCCAGCTCGGGTGGCGTGTCGATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGCCACTCGGTGGAGCCCTCGGTGGTTGCCCATGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCGCGGCAAGCTGGAACTGCTGGGCTACCGCATGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACATCGCGGAGCGCCGTAGCGACTCCAGCTACCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGACGCGCCCGCCGTGAGCAGCACCAGGTCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACACGTCAATGCGACAAAGGAGGGAGCACCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCAAGCGCGGAGACGTCTATGCCAAGGCGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCCCATGAGGTCCACGCGGAGTTGCTCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCATGGTGGACCGCATCTACGCGGCGTTCGACACCATGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017172|19|18|8873473-8882729|CRISPRCasFinder
CTTTCGACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CGTACAGGCTGGACTCGTGGAAGGTGCCGTAAAC
GTTTCAACCTACGCTCCCCTCGTTCATGAGGAGCGAC	CCGAGAGGTTGTCCACAGCTCGGCCAACTACGGAGAT
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CATAGCCCCGGCCACGAGTCTTGCCCGACCCTGGC
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CACGACGGATGCGCCTGCCCGCAGGCACGTGTG
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CGACCAGGCCGAGTGGAACACGCGTGAGGCCGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGCGGAGGTTCGCCACCACCTCGCGGTGCACGTG
GTTTCAACCCACGCTCCACGCGTTCACGAGGAGCGAC	CGCGCGCCGGGCGCACCTTCTGTTCTGTGCGTG
GTTTCAACCCACTCTCCTCGCGTTCACGAGGAGCGAC	GCGACACCGGAGGACACAGGACGTGGCTCTGTTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGGC	CTGGACCATGGCTGCTCGCAGATGGTGCTCGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TGATGTTCTCTGCCATGAGTGATTCTCGAAACGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GGCGCGGCCTTCCCGGCGCTGCCTGCGCTTGGG
GTTTCAACCCACGTTCCTCGCGTTCACGAGGAGCGAC	GACGACAAATCTCCATGCTCAACAAGGCCCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACTACGCGGTGGTGCGCGGACGCGACGCGCACGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GGCGCAGCTGCTCCACCATCACCCCCTCTACGTTGAT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACCACCGGCCCGAGGAGCGGCTCGCACGAGAG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CGAGGCGCCCACGCTCCCCACTGTTTGAAGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCAAC	TTCAACGCCGGCAAAGGTCTACGCGGACTTTCTCCG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GCCTCCGGGTCCGCGCGCTTCGCGTTGTGCGAGAG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TGGCGACGACTCTACTGCGCGCTACCACGAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGGCCGGCGTCCTGGAGGGTGCCGCCTGGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGATGCCATGCTTGCGGCTCGGAGCGCCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCTCCAGGATGCAGCAGGCCTACCTCAACGC
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CGGGCGCCTCTTTCGGTGGTAGGAGATAGACATGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGCGGCCGTCGCGCAGGGGACTGGCGTCGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGGCTTGCGCTTCTTGGGCCGCATGCGTTGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAAGAGCGAC	TGTCGTGGCACCACAGCAGCACCGGGTTCTTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCGAGAATCGGGCGGCACCGTCGAGTTGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCTCCAAGAGGCCTCGGTACTGCTCAACGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGAGCGGCTTCGACGGTCAACTCGGTGCTTGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGATGCCGTCCAAGTCACACCGGGCCGCGAGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCGTCGTCCAGCATCACGAGGGCCCTTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACATGACTAGGCGAGGAGGGCTTGGAAGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACTAGCTGCGCCGCTTTCCGGACCATTGCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCACGGGCGAACTGGCGCTGTACGAGCCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTTCCTGGCAGTCCGCGAGGACGCCATCATCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGGGGCTCCGGGCCATGATCATGGGGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGGATTCCCGCGCTCACGGGTGCAGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGTAGGCGGCGCCCCCATCGCCCCCGAGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCGCGACCTCGCGCGCTACATGGGCCTGGACTTCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCAGCAGCTCCAGCTTGCCCCGCCACTGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTTCATGCCGCCACCCGGGCGGGCTCCAGCCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCAATGAGGGCGCCGAGAATGGAGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGAGCGCTCGGGTGCTGTCTAGCTTCTGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCTGGGCGGTATCCGTGAAGTCCTTCACTCCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGGTGTCGAGCTGTATCAGCGCGGAAATGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCACCCGTGAGGTCCTCGTCGCCTACCGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGCGCAGGTGGGCGCTCACCGCGTCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTCGGTGGGCACAAAGCACAAGAGCTTCAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGACGTCTGGACGACTCCGCCAAGCAAGGTGGTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCCCGCCGTCTACCGTCGCACCACCCAGGCCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCTGGCCGCCCACCTTCGTACGCTCGGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTCCAAGCTGCAGCGACGTCTGCCGCGCTCAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACATTGTATGAACGACACGCCCCGCAGCTACTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTCACGTCGGCGGAGGCGCTGATGGCCAGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCTGGAGCTGACGCTGGATGCCATGGCGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCAGCCATGTGCTGCCTTCCGCACGGGAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGTCGCGGTGACGCCCAGGATGCGCGAGTTCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAATGAACGCGGAGCTGCGCCGGTGCGCCGCGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCAGCACCACGACCGGCGGGCCAGCTCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATGTACGCGCTCGCCTTCCTCTCGCGGGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCGTCTCGTGGCTCAGGTGTCATCCACCAATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCCCCGTACGCGGCCCGGTCCGTCATCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGAGGCAGCGCGAGGTGTTCGCCCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCCGAGCAGCGAGAACGTGACGCCCTCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGGGTCTGGTCGCTGTGGTGGATGCCCTGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCCGCGCCCGCATCGCCCCGACGCCCACGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCGTCCACCTGCTGGCCCATGCGGCGCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTGCCGGCGGGCGCAGCTCCGGCGGAAGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAACGGACGATGAGATGATTGAGCGGGCGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGTAGCCCGCGCTATCCGCCACTGGCTCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAGCCGAAGGGCGCCGCATCCTCGCCCCCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGACGCAACCGGGCTCGCGATTCGGCAGCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGGGCGGTCTCGGGTTCGCCACTGAGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGAATCGATCCTGCCCATCACCGTCCCAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGCACAACCTGGTGGGCTCCTTCGTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGCTCACCGTTGGCGCAATCCTCTCCTGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCAAGTCCGGCCCTCGCAAGGGGCGGCCGAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGCATCTGGAGGGGCTGCCGGTGAAGGCGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTGGTCCTCGATCGCGTTGTAGCGGATTGCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCCGGCATTCTCGTACCCCTTCGTCGAGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTACTGGCAGGCACGTCAGGCGGAGCTCGACTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCACTGGGGGCTCTTCTTGGGCGTGGCCCTGGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGTGGGTCTTCCGCCAGTTCACCTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGTGGGGGCACGTACACGGGCAACGCCAGTTATGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGAGCAGACGCGGCTTTCTTCTGACGCGGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGTCGAAGACGATGAAGTTACTGCGGATGTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCCAAGGTCCGTTTTCGCTGGCCGGAGGCGGAACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAGGACGGGCCATCCTGCGCGTCCTGCGATTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGGCGCCCACGTGCCCTGCCTGCCGCTCTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGTGGGCGGCGTGTTGTCGACGAGGACGGTGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGCTCAATCAGTTCACACGCTTCGGTGGAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CATCGAGCTGGCGCGCGTGAACGACCACCTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCGCGTCATCGCGTCCGCGGCCCAGTCCGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGATGTGGAGTGTCCAGAGTGCGAGTCCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCTGAGTGATTACCGTCCGTGTTGCCACCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATCCGGGCTTGAGCATCACCATAAATGGGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGAGCTCACAGGCATGACGTTGCCACGCAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCGCGCGCACGTCACAGCGAGGGAGGACTCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCTCGTGCGGGTAGTGGGGGTGGATGACGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCGCATCCGGTCAGCGCGCTTCGTGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGCGGACGGCAAGGTCTTCACCGCCGCGGTGGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCTAGGGCTACGCCAGCCACTTGCACTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCGAGGGTCCCGGCCATGCCGCGAGCAGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCCACGGGCTGTCCCGTCGTGTTCCGGTAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCCGCGCTGCAACGCGTAGCGCCAAACTCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCAGTCATCCACACCGCTGGGACGTTGGGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGTCCAATCGGCGACCCTCCACATCCTTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGGCGGCCAAGGTTCCGACATCCGGGCGGAGGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCGGGCGGGCAGTCGCGGACGTGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTCACTGCGGCAACAACGCAGGGGATGCAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGTCAGCAGTTCCAACAGGGGGGAGGAGGTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGACGTCGTGCTTCTCAGCCCATTTCATCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCCATTGCCGCCCACGTCTCCGCCACCCGTAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCGGGGTGGGAGGCGAGGGCGGCATCACCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGGCGCTCCAGGCCCAGCTCGGGTGGCGTGTCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCACTCGGTGGAGCCCTCGGTGGTTGCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCAAGCTGGAACTGCTGGGCTACCGCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGCGGAGCGCCGTAGCGACTCCAGCTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGCCCGCCGTGAGCAGCACCAGGTCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACGTCAATGCGACAAAGGAGGGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCAAGCGCGGAGACGTCTATGCCAAGGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCCCATGAGGTCCACGCGGAGTTGCTCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017172|19|2|8873473-8882729|CRT
CTTTCGACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CGTACAGGCTGGACTCGTGGAAGGTGCCGTAAAC
GTTTCAACCTACGCTCCCCTCGTTCATGAGGAGCGAC	CCGAGAGGTTGTCCACAGCTCGGCCAACTACGGAGAT
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CATAGCCCCGGCCACGAGTCTTGCCCGACCCTGGC
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CACGACGGATGCGCCTGCCCGCAGGCACGTGTG
GTTTCAACCCACGCTCCCCTCGTTCACGAGGAGCGAC	CGACCAGGCCGAGTGGAACACGCGTGAGGCCGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGCGGAGGTTCGCCACCACCTCGCGGTGCACGTG
GTTTCAACCCACGCTCCACGCGTTCACGAGGAGCGAC	CGCGCGCCGGGCGCACCTTCTGTTCTGTGCGTG
GTTTCAACCCACTCTCCTCGCGTTCACGAGGAGCGAC	GCGACACCGGAGGACACAGGACGTGGCTCTGTTCGA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGGC	CTGGACCATGGCTGCTCGCAGATGGTGCTCGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TGATGTTCTCTGCCATGAGTGATTCTCGAAACGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GGCGCGGCCTTCCCGGCGCTGCCTGCGCTTGGG
GTTTCAACCCACGTTCCTCGCGTTCACGAGGAGCGAC	GACGACAAATCTCCATGCTCAACAAGGCCCA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACTACGCGGTGGTGCGCGGACGCGACGCGCACGG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GGCGCAGCTGCTCCACCATCACCCCCTCTACGTTGAT
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	ACCACCGGCCCGAGGAGCGGCTCGCACGAGAG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	CGAGGCGCCCACGCTCCCCACTGTTTGAAGAA
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCAAC	TTCAACGCCGGCAAAGGTCTACGCGGACTTTCTCCG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	GCCTCCGGGTCCGCGCGCTTCGCGTTGTGCGAGAG
GTTTCAACCCACGCTCCTCGCGTTCACGAGGAGCGAC	TGGCGACGACTCTACTGCGCGCTACCACGAGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGGCCGGCGTCCTGGAGGGTGCCGCCTGGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGATGCCATGCTTGCGGCTCGGAGCGCCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCTCCAGGATGCAGCAGGCCTACCTCAACGC
GTTTCAACCCACGCTTCCCGCGTTCACGAGGAGCGAC	CGGGCGCCTCTTTCGGTGGTAGGAGATAGACATGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGCGGCCGTCGCGCAGGGGACTGGCGTCGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGGCTTGCGCTTCTTGGGCCGCATGCGTTGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAAGAGCGAC	TGTCGTGGCACCACAGCAGCACCGGGTTCTTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCGAGAATCGGGCGGCACCGTCGAGTTGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCTCCAAGAGGCCTCGGTACTGCTCAACGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGAGCGGCTTCGACGGTCAACTCGGTGCTTGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGATGCCGTCCAAGTCACACCGGGCCGCGAGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCGTCGTCCAGCATCACGAGGGCCCTTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACATGACTAGGCGAGGAGGGCTTGGAAGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACTAGCTGCGCCGCTTTCCGGACCATTGCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCACGGGCGAACTGGCGCTGTACGAGCCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTTCCTGGCAGTCCGCGAGGACGCCATCATCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGGGGCTCCGGGCCATGATCATGGGGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGGATTCCCGCGCTCACGGGTGCAGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGTAGGCGGCGCCCCCATCGCCCCCGAGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCGCGACCTCGCGCGCTACATGGGCCTGGACTTCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCAGCAGCTCCAGCTTGCCCCGCCACTGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTTCATGCCGCCACCCGGGCGGGCTCCAGCCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCAATGAGGGCGCCGAGAATGGAGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGAGCGCTCGGGTGCTGTCTAGCTTCTGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCTGGGCGGTATCCGTGAAGTCCTTCACTCCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGGTGTCGAGCTGTATCAGCGCGGAAATGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCACCCGTGAGGTCCTCGTCGCCTACCGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGCGCAGGTGGGCGCTCACCGCGTCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTCGGTGGGCACAAAGCACAAGAGCTTCAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGACGTCTGGACGACTCCGCCAAGCAAGGTGGTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCCCGCCGTCTACCGTCGCACCACCCAGGCCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCTGGCCGCCCACCTTCGTACGCTCGGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTCCAAGCTGCAGCGACGTCTGCCGCGCTCAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACATTGTATGAACGACACGCCCCGCAGCTACTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTCACGTCGGCGGAGGCGCTGATGGCCAGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCTGGAGCTGACGCTGGATGCCATGGCGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCAGCCATGTGCTGCCTTCCGCACGGGAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGTCGCGGTGACGCCCAGGATGCGCGAGTTCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAATGAACGCGGAGCTGCGCCGGTGCGCCGCGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCAGCACCACGACCGGCGGGCCAGCTCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATGTACGCGCTCGCCTTCCTCTCGCGGGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCGTCTCGTGGCTCAGGTGTCATCCACCAATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCCCCGTACGCGGCCCGGTCCGTCATCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGAGGCAGCGCGAGGTGTTCGCCCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCCGAGCAGCGAGAACGTGACGCCCTCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGGGTCTGGTCGCTGTGGTGGATGCCCTGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCCGCGCCCGCATCGCCCCGACGCCCACGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCGTCCACCTGCTGGCCCATGCGGCGCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTGCCGGCGGGCGCAGCTCCGGCGGAAGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAACGGACGATGAGATGATTGAGCGGGCGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGTAGCCCGCGCTATCCGCCACTGGCTCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAGCCGAAGGGCGCCGCATCCTCGCCCCCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGACGCAACCGGGCTCGCGATTCGGCAGCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGGGCGGTCTCGGGTTCGCCACTGAGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGAATCGATCCTGCCCATCACCGTCCCAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGCACAACCTGGTGGGCTCCTTCGTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGCTCACCGTTGGCGCAATCCTCTCCTGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCAAGTCCGGCCCTCGCAAGGGGCGGCCGAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGCATCTGGAGGGGCTGCCGGTGAAGGCGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTGGTCCTCGATCGCGTTGTAGCGGATTGCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCCGGCATTCTCGTACCCCTTCGTCGAGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTACTGGCAGGCACGTCAGGCGGAGCTCGACTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCACTGGGGGCTCTTCTTGGGCGTGGCCCTGGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGTGGGTCTTCCGCCAGTTCACCTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGTGGGGGCACGTACACGGGCAACGCCAGTTATGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGAGCAGACGCGGCTTTCTTCTGACGCGGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGTCGAAGACGATGAAGTTACTGCGGATGTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCCAAGGTCCGTTTTCGCTGGCCGGAGGCGGAACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAGGACGGGCCATCCTGCGCGTCCTGCGATTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGGCGCCCACGTGCCCTGCCTGCCGCTCTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGTGGGCGGCGTGTTGTCGACGAGGACGGTGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGCTCAATCAGTTCACACGCTTCGGTGGAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CATCGAGCTGGCGCGCGTGAACGACCACCTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCGCGTCATCGCGTCCGCGGCCCAGTCCGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGATGTGGAGTGTCCAGAGTGCGAGTCCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCTGAGTGATTACCGTCCGTGTTGCCACCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATCCGGGCTTGAGCATCACCATAAATGGGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGAGCTCACAGGCATGACGTTGCCACGCAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCGCGCGCACGTCACAGCGAGGGAGGACTCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCTCGTGCGGGTAGTGGGGGTGGATGACGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCGCATCCGGTCAGCGCGCTTCGTGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGCGGACGGCAAGGTCTTCACCGCCGCGGTGGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCTAGGGCTACGCCAGCCACTTGCACTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCGAGGGTCCCGGCCATGCCGCGAGCAGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCCACGGGCTGTCCCGTCGTGTTCCGGTAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCCGCGCTGCAACGCGTAGCGCCAAACTCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCAGTCATCCACACCGCTGGGACGTTGGGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGTCCAATCGGCGACCCTCCACATCCTTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGGCGGCCAAGGTTCCGACATCCGGGCGGAGGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCGGGCGGGCAGTCGCGGACGTGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTCACTGCGGCAACAACGCAGGGGATGCAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGTCAGCAGTTCCAACAGGGGGGAGGAGGTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGACGTCGTGCTTCTCAGCCCATTTCATCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCCATTGCCGCCCACGTCTCCGCCACCCGTAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCGGGGTGGGAGGCGAGGGCGGCATCACCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGGCGCTCCAGGCCCAGCTCGGGTGGCGTGTCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCACTCGGTGGAGCCCTCGGTGGTTGCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCAAGCTGGAACTGCTGGGCTACCGCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGCGGAGCGCCGTAGCGACTCCAGCTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGCCCGCCGTGAGCAGCACCAGGTCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACGTCAATGCGACAAAGGAGGGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCAAGCGCGGAGACGTCTATGCCAAGGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCCCATGAGGTCCACGCGGAGTTGCTCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017172|19|1|8875177-8882729|PILER-CR
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGGCTTGCGCTTCTTGGGCCGCATGCGTTGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAAGAGCGAC	TGTCGTGGCACCACAGCAGCACCGGGTTCTTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCGAGAATCGGGCGGCACCGTCGAGTTGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCTCCAAGAGGCCTCGGTACTGCTCAACGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGAGCGGCTTCGACGGTCAACTCGGTGCTTGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGATGCCGTCCAAGTCACACCGGGCCGCGAGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCGTCGTCCAGCATCACGAGGGCCCTTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACATGACTAGGCGAGGAGGGCTTGGAAGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACTAGCTGCGCCGCTTTCCGGACCATTGCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCACGGGCGAACTGGCGCTGTACGAGCCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTTCCTGGCAGTCCGCGAGGACGCCATCATCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGGGGCTCCGGGCCATGATCATGGGGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGGATTCCCGCGCTCACGGGTGCAGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGTAGGCGGCGCCCCCATCGCCCCCGAGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCGCGACCTCGCGCGCTACATGGGCCTGGACTTCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCAGCAGCTCCAGCTTGCCCCGCCACTGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTTCATGCCGCCACCCGGGCGGGCTCCAGCCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCAATGAGGGCGCCGAGAATGGAGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGAGCGCTCGGGTGCTGTCTAGCTTCTGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCTGGGCGGTATCCGTGAAGTCCTTCACTCCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGGTGTCGAGCTGTATCAGCGCGGAAATGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCACCCGTGAGGTCCTCGTCGCCTACCGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGCGCAGGTGGGCGCTCACCGCGTCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTCGGTGGGCACAAAGCACAAGAGCTTCAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGACGTCTGGACGACTCCGCCAAGCAAGGTGGTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCCCGCCGTCTACCGTCGCACCACCCAGGCCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCTGGCCGCCCACCTTCGTACGCTCGGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTCCAAGCTGCAGCGACGTCTGCCGCGCTCAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACATTGTATGAACGACACGCCCCGCAGCTACTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTCACGTCGGCGGAGGCGCTGATGGCCAGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCTGGAGCTGACGCTGGATGCCATGGCGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCAGCCATGTGCTGCCTTCCGCACGGGAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGTCGCGGTGACGCCCAGGATGCGCGAGTTCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAATGAACGCGGAGCTGCGCCGGTGCGCCGCGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCAGCACCACGACCGGCGGGCCAGCTCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATGTACGCGCTCGCCTTCCTCTCGCGGGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCGTCTCGTGGCTCAGGTGTCATCCACCAATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCCCCGTACGCGGCCCGGTCCGTCATCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGAGGCAGCGCGAGGTGTTCGCCCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCCGAGCAGCGAGAACGTGACGCCCTCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGGGTCTGGTCGCTGTGGTGGATGCCCTGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCCGCGCCCGCATCGCCCCGACGCCCACGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCGTCCACCTGCTGGCCCATGCGGCGCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTGCCGGCGGGCGCAGCTCCGGCGGAAGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAACGGACGATGAGATGATTGAGCGGGCGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGTAGCCCGCGCTATCCGCCACTGGCTCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAGCCGAAGGGCGCCGCATCCTCGCCCCCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGACGCAACCGGGCTCGCGATTCGGCAGCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGGGCGGTCTCGGGTTCGCCACTGAGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGAATCGATCCTGCCCATCACCGTCCCAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGCACAACCTGGTGGGCTCCTTCGTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGCTCACCGTTGGCGCAATCCTCTCCTGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCAAGTCCGGCCCTCGCAAGGGGCGGCCGAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGCATCTGGAGGGGCTGCCGGTGAAGGCGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTGGTCCTCGATCGCGTTGTAGCGGATTGCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCCGGCATTCTCGTACCCCTTCGTCGAGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTACTGGCAGGCACGTCAGGCGGAGCTCGACTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCACTGGGGGCTCTTCTTGGGCGTGGCCCTGGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGTGGGTCTTCCGCCAGTTCACCTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGTGGGGGCACGTACACGGGCAACGCCAGTTATGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGAGCAGACGCGGCTTTCTTCTGACGCGGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGTCGAAGACGATGAAGTTACTGCGGATGTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCCAAGGTCCGTTTTCGCTGGCCGGAGGCGGAACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAGGACGGGCCATCCTGCGCGTCCTGCGATTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGGCGCCCACGTGCCCTGCCTGCCGCTCTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGTGGGCGGCGTGTTGTCGACGAGGACGGTGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGCTCAATCAGTTCACACGCTTCGGTGGAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CATCGAGCTGGCGCGCGTGAACGACCACCTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCGCGTCATCGCGTCCGCGGCCCAGTCCGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGATGTGGAGTGTCCAGAGTGCGAGTCCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCTGAGTGATTACCGTCCGTGTTGCCACCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATCCGGGCTTGAGCATCACCATAAATGGGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGAGCTCACAGGCATGACGTTGCCACGCAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCGCGCGCACGTCACAGCGAGGGAGGACTCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCTCGTGCGGGTAGTGGGGGTGGATGACGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCGCATCCGGTCAGCGCGCTTCGTGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGCGGACGGCAAGGTCTTCACCGCCGCGGTGGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCTAGGGCTACGCCAGCCACTTGCACTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCGAGGGTCCCGGCCATGCCGCGAGCAGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCCACGGGCTGTCCCGTCGTGTTCCGGTAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCCGCGCTGCAACGCGTAGCGCCAAACTCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCAGTCATCCACACCGCTGGGACGTTGGGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGTCCAATCGGCGACCCTCCACATCCTTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGGCGGCCAAGGTTCCGACATCCGGGCGGAGGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCGGGCGGGCAGTCGCGGACGTGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTCACTGCGGCAACAACGCAGGGGATGCAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGTCAGCAGTTCCAACAGGGGGGAGGAGGTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGACGTCGTGCTTCTCAGCCCATTTCATCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCCATTGCCGCCCACGTCTCCGCCACCCGTAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCGGGGTGGGAGGCGAGGGCGGCATCACCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGGCGCTCCAGGCCCAGCTCGGGTGGCGTGTCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCACTCGGTGGAGCCCTCGGTGGTTGCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCAAGCTGGAACTGCTGGGCTACCGCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGCGGAGCGCCGTAGCGACTCCAGCTACCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGACGCGCCCGCCGTGAGCAGCACCAGGTCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACACGTCAATGCGACAAAGGAGGGAGCACCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCAAGCGCGGAGACGTCTATGCCAAGGCGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCCCATGAGGTCCACGCGGAGTTGCTCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
	CCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGCCCGCCGTGAGCAGCACCAGGTCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACGTCAATGCGACAAAGGAGGGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCAAGCGCGGAGACGTCTATGCCAAGGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCCCATGAGGTCCACGCGGAGTTGCTCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

>NZ_CP017172|19|2|8882051-8882729|PILER-CR
	TTCGGCTTGCGCTTCTTGGGCCGCATGCGTTGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAAGAGCGAC	TGTCGTGGCACCACAGCAGCACCGGGTTCTTGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCGAGAATCGGGCGGCACCGTCGAGTTGCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCTCCAAGAGGCCTCGGTACTGCTCAACGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGAGCGGCTTCGACGGTCAACTCGGTGCTTGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGATGCCGTCCAAGTCACACCGGGCCGCGAGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCGTCGTCGTCCAGCATCACGAGGGCCCTTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACATGACTAGGCGAGGAGGGCTTGGAAGCCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACTAGCTGCGCCGCTTTCCGGACCATTGCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCGCACGGGCGAACTGGCGCTGTACGAGCCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTTCCTGGCAGTCCGCGAGGACGCCATCATCCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGGGGCTCCGGGCCATGATCATGGGGGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGCGCAGTACCAAGTGGCCGTCGACTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGGGATTCCCGCGCTCACGGGTGCAGGGCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGTAGGCGGCGCCCCCATCGCCCCCGAGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCGCGACCTCGCGCGCTACATGGGCCTGGACTTCGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCAGCAGCTCCAGCTTGCCCCGCCACTGCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCTTCATGCCGCCACCCGGGCGGGCTCCAGCCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCAATGAGGGCGCCGAGAATGGAGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGAGCGCTCGGGTGCTGTCTAGCTTCTGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTCTGGGCGGTATCCGTGAAGTCCTTCACTCCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGGTGTCGAGCTGTATCAGCGCGGAAATGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCACCCGTGAGGTCCTCGTCGCCTACCGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGCGCAGGTGGGCGCTCACCGCGTCGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTCGGTGGGCACAAAGCACAAGAGCTTCAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGACTTGGAGCACCGAGGGCCGCGTCGTCGAAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGACGTCTGGACGACTCCGCCAAGCAAGGTGGTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCCCCGCCGTCTACCGTCGCACCACCCAGGCCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTTCTGGCCGCCCACCTTCGTACGCTCGGCCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTTCCAAGCTGCAGCGACGTCTGCCGCGCTCAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACATTGTATGAACGACACGCCCCGCAGCTACTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGTCACGTCGGCGGAGGCGCTGATGGCCAGGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCTGGAGCTGACGCTGGATGCCATGGCGGCGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCAGCCATGTGCTGCCTTCCGCACGGGAGAGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGTCGCGGTGACGCCCAGGATGCGCGAGTTCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAATGAACGCGGAGCTGCGCCGGTGCGCCGCGAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCCCAGCACCACGACCGGCGGGCCAGCTCTCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGATGTACGCGCTCGCCTTCCTCTCGCGGGCTGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCTCGTCTCGTGGCTCAGGTGTCATCCACCAATC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCCCCGTACGCGGCCCGGTCCGTCATCGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGAGGCAGCGCGAGGTGTTCGCCCGCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGAGCCGAGCAGCGAGAACGTGACGCCCTCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGGGTCTGGTCGCTGTGGTGGATGCCCTGCTGGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCCGCGCCCGCATCGCCCCGACGCCCACGCC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACGTCGTCCACCTGCTGGCCCATGCGGCGCTT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTGCCGGCGGGCGCAGCTCCGGCGGAAGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAACGGACGATGAGATGATTGAGCGGGCGCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGTAGCCCGCGCTATCCGCCACTGGCTCAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAAGCCGAAGGGCGCCGCATCCTCGCCCCCCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGACGCAACCGGGCTCGCGATTCGGCAGCTCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCGGGCGGTCTCGGGTTCGCCACTGAGTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTGGAATCGATCCTGCCCATCACCGTCCCAAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGAGCACAACCTGGTGGGCTCCTTCGTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GATGCTCACCGTTGGCGCAATCCTCTCCTGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCAAGTCCGGCCCTCGCAAGGGGCGGCCGAACGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGCATCTGGAGGGGCTGCCGGTGAAGGCGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGTGGTCCTCGATCGCGTTGTAGCGGATTGCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGCCGGCATTCTCGTACCCCTTCGTCGAGGCGGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GTACTGGCAGGCACGTCAGGCGGAGCTCGACTACCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGCACTGGGGGCTCTTCTTGGGCGTGGCCCTGGCGCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGATGTGGGTCTTCCGCCAGTTCACCTTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGTGGGGGCACGTACACGGGCAACGCCAGTTATGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGAGCAGACGCGGCTTTCTTCTGACGCGGACGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATGTCGAAGACGATGAAGTTACTGCGGATGTTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TCTCCAAGGTCCGTTTTCGCTGGCCGGAGGCGGAACT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGAGGACGGGCCATCCTGCGCGTCCTGCGATTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACAAGGCGCCCACGTGCCCTGCCTGCCGCTCTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGTGGGCGGCGTGTTGTCGACGAGGACGGTGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GGCGCTCAATCAGTTCACACGCTTCGGTGGAGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CATCGAGCTGGCGCGCGTGAACGACCACCTCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCGCGTCATCGCGTCCGCGGCCCAGTCCGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCCGATGTGGAGTGTCCAGAGTGCGAGTCCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCTGAGTGATTACCGTCCGTGTTGCCACCTGCGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AATCCGGGCTTGAGCATCACCATAAATGGGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGAGCTCACAGGCATGACGTTGCCACGCAGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCGCCCGCGCGCACGTCACAGCGAGGGAGGACTCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGCCTCGTGCGGGTAGTGGGGGTGGATGACGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCCGCATCCGGTCAGCGCGCTTCGTGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ACCGCGGACGGCAAGGTCTTCACCGCCGCGGTGGTGG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCTAGGGCTACGCCAGCCACTTGCACTGCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGCGCCGAGGGTCCCGGCCATGCCGCGAGCAGTA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CTGGCCACGGGCTGTCCCGTCGTGTTCCGGTAGGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCCGCGCTGCAACGCGTAGCGCCAAACTCCCTC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGCAGTCATCCACACCGCTGGGACGTTGGGCGA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCGTCCAATCGGCGACCCTCCACATCCTTGT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTGGCGGCCAAGGTTCCGACATCCGGGCGGAGGCGAA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	AGGGCGGGCGGGCAGTCGCGGACGTGGGTGCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCTTCACTGCGGCAACAACGCAGGGGATGCAGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TTCGTCAGCAGTTCCAACAGGGGGGAGGAGGTGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGGACGTCGTGCTTCTCAGCCCATTTCATCAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCCATTGCCGCCCACGTCTCCGCCACCCGTAG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCGCGGGGTGGGAGGCGAGGGCGGCATCACCCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GAGGCGCTCCAGGCCCAGCTCGGGTGGCGTGTCGAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GCCACTCGGTGGAGCCCTCGGTGGTTGCCCAT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CGCGGCAAGCTGGAACTGCTGGGCTACCGCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	ATCGCGGAGCGCCGTAGCGACTCCAGCTACCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGACGCGCCCGCCGTGAGCAGCACCAGGTCCTGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACGACACGTCAATGCGACAAAGGAGGGAGCACCTGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCGCAAGCGCGGAGACGTCTATGCCAAGGCGGCGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCACCCCCATGAGGTCCACGCGGAGTTGCTCGCGGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCAGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACTGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGACGTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGACCCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
	CCGCTCGACTGGTGGCGTTGACCTGTTTCTCTCCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGACGCGCCCGCCGTGAGCAGCACCAGGTCCT
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	GACACGTCAATGCGACAAAGGAGGGAGCACCTG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCGCAAGCGCGGAGACGTCTATGCCAAGGCGGC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CACCCCCATGAGGTCCACGCGGAGTTGCTCGCG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CAGTTCTGCGCCCTGGGCGCGAGCATCAGCGACCA
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	TGGAGCGCCAGCCCAAGCCCCATCCGGTGAGGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCAGCGGCCTCCCCGCCTCGACGAAGGGGTACGAC
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC	CCATGGTGGACCGCATCTACGCGGCGTTCGACACCATG
GTTTCAACCCACGCTCCCCGCGTTCACGAGGAGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140800336.1\|8884888_8885803_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl\|CDD\|187820
NZ_CP017172.1\|WP_140800339.1\|8888261_8890565_-\|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP017172.1\|WP_140795887.1\|8883209_8884238_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP017172.1\|WP_140877823.1\|8857519_8860297_-\|TonB-family-protein	unknown	unknown	gnl\|CDD\|367555
NZ_CP017172.1\|WP_140800337.1\|8885841_8887584_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	cd09642_cas8c_CAS-I-C	gnl\|CDD\|273839
NZ_CP017172.1\|WP_140877829.1\|8872322_8873039_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|283403
NZ_CP017172.1\|WP_140800332.1\|8870473_8871163_+\|response-regulator	unknown	unknown	gnl\|CDD\|381108
NZ_CP017172.1\|WP_140800333.1\|8871691_8872285_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140877825.1\|8861975_8862617_+\|TIGR02265-family-protein	unknown	unknown	gnl\|CDD\|131318
NZ_CP017172.1\|WP_140795878.1\|8860961_8861462_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP017172.1\|WP_174258996.1\|8887583_8888240_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|187534
NZ_CP017172.1\|WP_174259442.1\|8893272_8895348_-\|beta-propeller-domain-containing-protein	unknown	unknown	gnl\|CDD\|378255
NZ_CP017172.1\|WP_174259441.1\|8864680_8867080_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_011556933.1\|8882910_8883201_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP017172.1\|WP_140877831.1\|8884250_8884892_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
NZ_CP017172.1\|WP_140795894.1\|8891721_8893116_-\|MATE-family-efflux-transporter	unknown	unknown	gnl\|CDD\|240536
NZ_CP017172.1\|WP_140800331.1\|8867307_8869605_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP017172.1\|WP_140795893.1\|8890994_8891708_+\|esterase	unknown	unknown	gnl\|CDD\|227283
NZ_CP017172.1\|WP_140795880.1\|8862706_8863861_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369473
NZ_CP017172.1\|WP_140795881.1\|8864306_8864675_+\|response-regulator	unknown	unknown	gnl\|CDD\|381118

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140800336.1\|8884888_8885803_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl\|CDD\|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	1.27789e-162
NZ_CP017172.1\|WP_140800339.1\|8888261_8890565_-\|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_CP017172.1\|WP_140795887.1\|8883209_8884238_-\|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_CP017172.1\|WP_140877823.1\|8857519_8860297_-\|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.	8.21338e-14
NZ_CP017172.1\|WP_140800337.1\|8885841_8887584_-\|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_CP017172.1\|WP_140795881.1\|8864306_8864675_+\|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_CP017172.1\|WP_140800332.1\|8870473_8871163_+\|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.	2.87689e-18
NZ_CP017172.1\|WP_140877825.1\|8861975_8862617_+\|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.	1.22007e-66
NZ_CP017172.1\|WP_140795878.1\|8860961_8861462_-\|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_CP017172.1\|WP_174258996.1\|8887583_8888240_-\|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_CP017172.1\|WP_174259442.1\|8893272_8895348_-\|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_CP017172.1\|WP_174259441.1\|8864680_8867080_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.30852e-41
NZ_CP017172.1\|WP_011556933.1\|8882910_8883201_-\|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_CP017172.1\|WP_140877831.1\|8884250_8884892_-\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	1.19479e-42
NZ_CP017172.1\|WP_140795894.1\|8891721_8893116_-\|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_CP017172.1\|WP_140800331.1\|8867307_8869605_+\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.4341e-44
NZ_CP017172.1\|WP_140795893.1\|8890994_8891708_+\|esterase	gnl\|CDD\|227283	COG4947, COG4947, Uncharacterized protein conserved in bacteria [Function unknown].	2.41182e-75
NZ_CP017172.1\|WP_140795880.1\|8862706_8863861_-\|hypothetical-protein	gnl\|CDD\|369473	pfam07705, CARDB, CARDB. Cell adhesion related domain found in bacteria.	8.86972e-08
NZ_CP017172.1\|WP_140877829.1\|8872322_8873039_+\|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.	4.42364e-14

>NZ_CP017172.1|WP_140877829.1|8872322_8873039_+|alpha/beta-fold-hydrolase
MSTSTTSPSAVGPRWLYLHGFASGPDSKKGVAVARHYEDQGIPVERLNLRVPSLEQLRLSAMLDTVLAAMGGPEERVVLIGSSLGGLTAARVAEQDARVCALVLLAPAFRVVPQLRRRMGDAAWRHWQTSGWIETDDFVTQQKARIHSGFIADAEAVDTRTGGWPDVRVPTLIIHGRQDDTCDVQNSRQWAEGKRHVRLVEVDDGHELTASLPRILEETEVFLHPWGARGPRAHSSMP
>NZ_CP017172.1|WP_140800333.1|8871691_8872285_+|hypothetical-protein
MRKQSMWVAVVGVLCVGTDAVAADWNGYASLGAGITLDHLSNFRTKGPALHGYLGLETPPGLSVGLLAEISETWGQQFPDAMRPGRLERSQLDYRAVGIEARLRFFQDKPITPWVGARLSKSWGSTFTPDDVGTWLRQNIDTTSMAFRVGVDGWFSDRWGVSVSTGFQFCDVKLTSNALNQCAKLMQSVIAGPVLRI
>NZ_CP017172.1|WP_140800332.1|8870473_8871163_+|response-regulator
MSRPLQHLLLVEDDLAWRERLTVVAHAEGVKVSHAADGQEALDWLCTRPRASHPDLILLDLLLPRMDGWELYGQLRTNARLRHLGVLMFSGALSGQEPPLDGVVGYLRKPHAPEAADGALRAQLRGLPELPSRDSAEPYALHLPEDVSLPLRTLPGALSHAVRLHLLRAAELAGTELPLASTWLMALPGTPPSLLVTVDGVQVELEVDDARRRLTVSDVTLSPNLRHGA
>NZ_CP017172.1|WP_140800331.1|8867307_8869605_+|HAMP-domain-containing-protein
MSGRARFAWALVVGLLGHALNRFPVELIPGIDILLGFFLIIPAAPLLGPWCAGLAAGIAMSVTVQMWGHPWSMLGSMMEGVVLGALTRRYWPLQADGIFWLGGIPYLIVSYHLGEDVTATSTFAIAFKQALNSLVPALLTQVVLMTPMARARLWPLLTPALRTFTLSSAVGSALLLALVLPLLMVGTLEGRARYAAERRRMDDQGLSTAHLLAETVDAELSTAQSQTALLASVVMDWWEREGERPPQPQLEELLRDWVYHSAFALNCSIGDSDGSLVAIWPPLGVAAQPVAGSNFADRAYFRDVRSKRAPVVSGVFAGRATVTGPVMVAVAPLLRQQRFEGFTSVAINLPRMRAVAQERLAPGQRALLVDPDGNVAFDTGATPGPEPQSLKGTALGEMLSTLPATGTRTYDTEPQAPPLRRTLGARHLATATLLQPGWRVLVEHPMHDMDFSVIGTYSALLATLALALVLAIPVTRLLTRMLSRPVEAVSHAAGRMAAGERDVRAFGALHHSGAIEVEKLGLAFDEMAARLQRHLEEVERVSQAKAAFFSIASHELKTPLATLKLRLQRLRPDTVRQQDLVLMDRQVDRLARLVNQLLDVSELASGRLSLAQVPLELSALVRRVSERRAASAPQHPLKLSLERVDGWWDEPRLEQVVYNLVDNAIRYSPEGGPVEVVLRREDGDALLEVKDRGVGLGPRGGEELFSRALRGGTLSTISRVEGLGVGLYLSREIITRHGGSIHLAAREGGGTCATVRLPRNDPREA
>NZ_CP017172.1|WP_174259441.1|8864680_8867080_-|PAS-domain-S-box-protein
MSAWEVEVRRIPAAQALPRLALRDGLPRLLEVVASLMRRDSPGGVEDGLGDIPDRHAIERLGEGFDLRQVVTEYRLLRACVLRLWTSRENATHRPEAELVFHEAMDEAVAASVSRYSLARERTLQALDRISTAALGSADAAELLPALLQVLRETVAVVDVAAVLLLEEDVLRVESVVGTGMAVGDVVRMGEGFTGTIAATRQPLLVRAARTDSRVSEPSLRDADLSALFGVPLLLGEQLMGVVLMGSRATHELSEEDQFLFRAMAARTTALLLQAQAHAREREARAVAEASLERLRESEAGLRRWAQVFKRLGVGVAVVDAAEERLREVNPAFARMHGYSPEELTGRRLEDTYAPEARGVLPRHVAVANSKPSHEYESLHIRKDGTRFPAFTHVTAFKDEVGRVVQRVATVVDITQRRAMEMDRQRLLGAIEAERARLASVLDQMPAGVFIADAPSGRLVMASRQVEVITGKPFHPSASMQDYVEDYGVSLRPDGRPYAMEALPLARSLRHGEVVQGEEMLIPREDGQYVTVLLSSSPIVDREGTIIAAVATMVDVSERRRAQEAALQAVRFGERLIAIVSHDLRNPLNAIQLSATQLLHSEALPERERRLVTRIARSGDRMKRMISELLDFTRGRLGGGIPIQRTAGDLRSVVRLGVDELEAAWPERKLAFRVEPGRYEGEWDEDRLLQVVSNLGGNALQYSPADAPVSFKLYDGGDFVVLEVHNPGEPISPEMLPRLFDPFRRGAMEGVGGGSSSGLGLGLYIVEQVVKGHGGRIEVTSTAQAGTAVRVTLPRLPTG
>NZ_CP017172.1|WP_140795881.1|8864306_8864675_+|response-regulator
MSTPNLVLLVEDHADSRELLEEFLTLEGFTVETAGNGLSAWERLSRPPLPDAVLLDLMMPVMSGWELMRHVREDARLSTLPVVVVSGAGSSQPLPEGIRATVPKPVDLFELRATLERVVSPS
>NZ_CP017172.1|WP_140795880.1|8862706_8863861_-|hypothetical-protein
MTRNHGVSTLTALFLLTGCEGTLPEESPATIDMEVQRQEAKETGLDLSVVDLSASCAATALTLSAAIKNERPTGIGNSTAAVYAGTPGAGGVRLGTISVPWLVGGETFPFSLSYTVPEGTTKVVVVADEDGTYPEDDEDNNFASIDFEIPCATNQQPVASCQSVTVPANAACQGSASIDNGSFDPDGFPGPFSVEQSPAGPYGLGTTSAQLLVSDGAASSTCSANVTVVDVSAPTPGANRGLVIQPVLGSDYVLVPLSDCAMPAVDNCGGELDLDASASIIRVTSDESNDALSLLRLLACDDIKLTPDRKSAMVRAEAALLGNGRVYNFTYAVQDASGNSAIGTCNVKVPALLANPAIDSGVVYCQGDNCPSGSRFPGLLCSLL
>NZ_CP017172.1|WP_140877825.1|8861975_8862617_+|TIGR02265-family-protein
MELRLPPRLVREPAPPQPLGPDAMRELRQRCALATPEDTARGMFFRGVLETVRRVGGSAMEQLCRQSLPEKRYIDFFSYPITQFLPLAFQAAGLLSEHCGGMAAAHRVMGQKAAQDFLESVAGRTLLMLAYDEPRLLLGQLPTGFLAAVSYGERSMVWTGPRSGRFVMKRDFMPTAYHEGVLHAALEAVGARDIGVQGRELGLLDTEYALSWR
>NZ_CP017172.1|WP_140795878.1|8860961_8861462_-|helix-turn-helix-domain-containing-protein
MSLARTHKVDAVKTHLEGPAPPRKRPRPQPRSPADRARKSREQLESRLAESVGEAARGARLLAGLTQADVAERVGIAAEVYGRMERGKMMPSVPTLFRLCLALRLSADVGLGLATAASVGAALWEGDSGHRDQLPEMRKVLRTLRRMSRSQLNLMNQVAAAILPER
>NZ_CP017172.1|WP_140877823.1|8857519_8860297_-|TonB-family-protein
MPGTRAHAQDAGTPEDGGAARAERELQRTDAGWAVETDAPLSEDAGVPEPAFIPPAMVRDSPAPYPPGLASDGVAGVVKLELLIDDAGEVESATLMEGLHPLLDRAALHAAPSLRFAPATLDGLPVAVRIFFEYRFEAPAPGMSEGATPAAPITLKGLVRTKGNRRPLVGATLVSDAHPDAPVQTDVDGRFEARWPAGVHAVRITAPGHKSGVFREGLKANEALEVVYGLEPLIINPYETVVRGDRERTEVSRVTLHDAELREVPGTMGDPFRVVMLLPGVGSMVSGVAYPVVRGSQPAATGYFLDGIRVPILFHLFLGPAVIHPDFIDAIDFYPGSPPPRYGRLMGGAIDGRLSRPRDDGVHGSAYADLINAGFFIETPFKDTGTNVSLAGRYSYTPWLIALAANQLQAPPPPGRENPKVVLDFWDYQGRVEQRLGEGTLRLFAFGSSDTFGSEAHDEWGDTAMQSIIFHRVDLRHRHPVGPGELEVGGTWGLDRFAIVSRSPPGEATEIHIDQGHWSARLGYTATLSPSATLRAGADVEHKRAIVELLQQDGGSDADVEVAPVALGTFMGAWTELVWQPHEKWAVVPGLRVDSYHLSPGIDRRALEPRLTVRHKVSETLTLKGGAGLFHQPPTTLISLPVVDVGSLLLGLQQGVQLSVGAEWKAWRGLEVGLDVYLNPMLRTLELTPFADEGMVDDDPPDTGTPPAGLRRGMQLGDGGGIPDRSDFDFPDFRSSGMAYGMEFLLRHPLGDNWFGWLSYSLQRSTRRTRFHRYDAEGHRVGEAEADLPFAFDQTHILNLVLSYKFANNITLGGVLHFNTGRPEYGTLGTQTHRPGEDASGRPAWVKADRDRVDRLPAFLRFDVRLSKSWVHDTFSLEAYLDMLNVTLRRETLGFEYEGGNGFPLRKEAVGLPIALPILGVKGRY
>NZ_CP017172.1|WP_011556933.1|8882910_8883201_-|CRISPR-associated-endonuclease-Cas2
MTVLICYDVRVSDPQGPRRLRKIARACRDHGVRVQYSVFECVLEPKDWVVLRARLLGAFDSECDSLRFYFLSEDDARKTEHHGARAPLDVEGPLVL
>NZ_CP017172.1|WP_140795887.1|8883209_8884238_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MTTALNTLFITAEGTRLNKEGECVVVTVQDQKKAEVPLRHLRSVVCLTRAWLTPELMESCLEAGIHVSFFGMTGRFLARVEGVPGGNVLLRRQQYRAADDIARSVAISRALVVGKLGNARQFVLHARRDAAPERQEALSETARRLSEHLRALTRVEDLEQVRGLEGIAARDYFESFPALLKKSAQGFEFDGRNRRPPRNPLNAMLSFGYALLAQDCAGALAGVGLDPAVGFLHEDRPGRLSLALDLMEEFRAPVVDRLVFSLVNRGQLKPGDFRTESAGAVLLKDDARKTFLVAYQEAKQVGVRHAFLGQETTWGMAPHLQSLLLARHLRGELDGYPPFAMR
>NZ_CP017172.1|WP_140877831.1|8884250_8884892_-|CRISPR-associated-protein-Cas4
MSADCETWVALSALQHLLYCERQAALIHVERQWREDVNTASGRLLHERVDLPGHDARVGRRVERAVLLGSQRLRVSGRADMVEYQRDAKGAGWRPYPVEVKRGRRKAGEADRVQLCAQALCLEEMHGVDVPEGALFYGVEHKRAAVRFDAELRQRTEDAIARMHEVLRRQEVPVVVRAPRCDGCSLEPLFLPGVTAGQRSAQDFLTRWMDEDG
>NZ_CP017172.1|WP_140800336.1|8884888_8885803_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTDLKQRHDFVLFFDVLDGNPNGDPDAGNLPRIDAETGHGLVTDVSLKRKVRNFILLTQEGKQGLDIFVKEKAILNNRIADAYKSLGIDLNEKPTRAEDGKKRTDKGFAQGSEVDKGRAWMCKTFFDVRTFGAVMSTGANAGQVRGPVQLTFARSVDPIVSQEHSITRMAVATEGEAEKQGGDNRTMGRKNTVPYGLYRAHGFVSPHLAKQTGFGTADLELLFQSFTHMFELDRSAARGLMSMRKVVVFKHGSELGNAPAHALFDRVHAVRAQPEKPARSFSDYEVRVDKAGLPQGIEVLELVG
>NZ_CP017172.1|WP_140800337.1|8885841_8887584_-|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MMLTALNDFARERGLTDDPLYETKPVDFFIRVSAAGKFVSLESTAGEDGRGKPLSIPRLPQRSVNIAAGFFADNPKYVLAYEKDAPKAKAGGVEKRVARLDAFLKPVREVAVETKDPEARAVESFLTSEAERRKVLAARDEDEWTGSELLAFVVGDATTPVHQNPAIRACWERRSGEKRALGRTARCLVTGLEGVVALTHPKLKNVPEAQSSGASLVSFNAPAFSSHGLEQGDNAPISQEAALGYVLALNDMLRRTEQRRFRQGIQLGDGSVLVFWTRASPSEESLLLSWMDPTEEDLQRFTESPLHGLQPGALDDRAFYAVTLTGNAGRVAVRDWFESRVGEVKRNIRRYFDDLRIGNAPAGPTPIYRLLNAVEAPSGRGLSPDVATRMVGAALRGLHFPRQLLTSALDRLRLPPADDRFEREQLRLRVALIKATLLRLPRSGTTPLEVTVSLDKNNASQPYVLGRLFAVLERLQGAALKDLNATIRDRYFGAASRNPVTVFPRLLQLSVHHASKAGENGRWLERTKGEVMALLPPERFPRVLGLEDQGLFAVGYYHQREAFFTKRETAASAESDAASS
>NZ_CP017172.1|WP_174258996.1|8887583_8888240_-|type-I-C-CRISPR-associated-protein-Cas5
MASTTGRRFRVRARGPVACFTRPEMKAERVSYEVMTPSAARGVLEAILWKPAIRWHIHEIAVLAPVKWTSFRRNEVNSRATVGRFDYAADEDRAQRNTVALRDVDYVITASFTLLPGKAGPEDNARKFEDMFERRLERGQFFHAPYLGCREFAARVEPAEDGLLPHEAGSGRRPLGLMFYDFVFDVPGAPVRPEFFQAFLEDGVLHVPPRAQVLGGDS
>NZ_CP017172.1|WP_140800339.1|8888261_8890565_-|CRISPR-associated-endonuclease-Cas3''
MQTHMLACAARHVGGGGSAMKKELGLSEQSAVPRVVTAEPLAHVTEDGRPHLLREHLEAVGQWAARLAPREDLRAPALATGRWHDLGKYTQDFWYRIRAENGFEAHLEKEGALERDHSTAGALWSLSRDRRLLPLALAIAGHHAGLPDLAAFKERLGRKEKQALLADARARCDVPALLDGPLGFEPDALVRLEPLRLELWTRMLFSLLCDADFLDTEAFFDASRGSEREVPVTLSQLAERLRGFLDEKQRVAPDTEVNRVRREVLSAAVEAASLHPGVFSLTVPTGGGKTLTSMAFALEHARRHGLQRVIVAIPYTSIIEQSADVYRQAFQGLEHAVIEHHSAVDPEKETALNRVASENWDAPVIVTTTVQLLESLFARRPSACRKLHRVARSVIVLDEAQTLPPSLLAPILDGLGALVKDYDCSVVICTATQPALGRRPDFQEGLPDAREIVPASVRAFERLRRVRVRWPTLGHKLPYTELADAVAAERDVLAVVHLRDDARRLCELVDERLGHQETLHLSALMCPEHRSEVLADIKARKRRGEPVRLVATQLVEAGVDLDFRVVFRGLGGLDSLAQAAGRCNREGLLDGLGELCVYEPETQPPRGVPRAAQDVTRGLLEQAPDLDLFAPASFQRYFERLYATRKLDEKGIQDLRAKLQFDAVSKAFKLVEDDWSASVVVPYANREALLDALRERGPSRERLRALQRFTVTVPRKVREAWLARELARLAAETVAYLGPEHTSAYHERFGLLLDRVGILDPSFLIPG
>NZ_CP017172.1|WP_140795893.1|8890994_8891708_+|esterase
MNREYHRWYSERLHRDMELLIFGHSGEPVLLLPTSKGRFFQAEDFGLIGAIADRVQSGRYIVVCPDSVDEESWFNTAIHPADRVRRHQQWEDYLLHEVVPLLKSRSTGGRLTLAGCSFGGFHSYNIGLRHPHVFRRLLSMGGKFETDEFLDGHHDSDVYFHSCTEWLPNLTDPAQLSALQRVEMVLAVGEHDFCRPSNEHLSNLLWKKDIGNHLSVWQGGTHDWPVWRQMIQQYLPW
>NZ_CP017172.1|WP_140795894.1|8891721_8893116_-|MATE-family-efflux-transporter
MSTAVLPMSSVNSPRTELRELARLAVPIAIAQGGQALMGLVDTLVVGRAGTSALAAVGLGNGLYFAVSSFGIGLMMGFDPMISQAIGARQFTRARALLWQGAWMAFCVGAMLATLMTLAPRLLPLAGISETEAAGASQYLAWRAPGMPMMLMFLTMRSYLQATAFTRPLVIATVVANIFNLLGNLLLVFGGANLPAWFGPLREVPALGVAGSAMATSASIGIELLIAVLFIRSRKVEGAPARRLPVWADLSRAIRLGLPIGLHICAEVGVFALAGVLAAGLGPASVGAHQIAISFASVSFTVAMGIGNAGSVRVGWAVGAHNTPQARLSGFMALAGGAGFMALSGLVFALFPHTLAKLAGAPADVLPLLIPLLMVSAIFQVFDGAQGVGAGVLRGAGDTRFTFLANMVGHYAIGLPVTLLLAFKLGLGVVGIWWGLCAGLISVAVALVWRFNRMSAGTLRPVEA
>NZ_CP017172.1|WP_174259442.1|8893272_8895348_-|beta-propeller-domain-containing-protein
MVAVVAAGCDEGNKPLSPVDNEPVQQEARLESFPGCEALEQHIEDTATKQMRAALESYKQYAYGGGRGGEAPPMTGAPQEDSSGGGGRPNDYTGTNNQVAGVHEADFVQNDGTRIFVLSGPRLYIHRSWPAEQLTRTAALEVEGWPLEMLLDAERNRLVITSGVAEDRLGTVGGGRGMDDMPVIDCAGFGCGYAYSNTVKVTVVDVADLEAPRVLEQIYLPGSYINARRVDSAVRLVFSDGFRWPADVRLYPEYSPGLFDDRGRLVASIDALIKQNEQRIRAQSLEHWLPKGRRVTADGEVKPLAYDCTSFYRANGPTGLGLVSVLSLNLDAEASSPSRTSVVGLPGEVYASHEALYVASRHWWWWPEPGQTTHTYLHKFDIRDPDQATYVGSGTVEGYIVNQFAMDEREGVLRVATTVELPPENPGTGNGGDTAWTPPETVNRVVTLREQDGRLKELGRSEDLARGERIFSARFMGTRGYVVTFRQVDPLFTFDLSDPANPRKVGELKIPGFSTYIHPLGDTHLLTFGEHRNEDGTWQDRALKLSLFDVSDLAQPKETFTHQLGSMGSHSEALYEHKAFTYFPAKGLLALPFTDWDYNAYDYWSGFRSELRVFRVDTATGFSPVGTVSMRDMYQSFNFRNWSWYWQPTVRRSIMADDYVYTISDAGLRVSHVDSLQTPLVTAPFHPPMLP

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP017172_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP017172_20

9408211-9408660

Orphan

Consensus_repeat	Method
GNTGGAATGAACGTTCCNTCCACNGC	CRT

7 spacers

csa3

The CRISPR arrays of NZ_CP017172_20

>merge|NZ_CP017172|20|9408211-9408660|CRT
GGTGGAATCAGCGTTCGTTCCACTGCGTGCAGATGCGCTGCGGTGAACGCTGCCAGTTGGAATGAACGTTCCGTCCGCAGCCTGCGGTTACGGCAGAGTGGGGCCTGCATCTGACTGGATTGAACGTTCCTTTCACTGCCTGCTGCTGCGGTCGGGCTCACCGTCTCAAGCTGGAATGAACGTTCCGTCCACTGCTCAAGGCCGCGAGCGAGGTGCTCACTCCTGGCTGGAATGAACGTTCCGTCCACTGCTCAAGGCCGTAGGGTGGAGTGCTCATCCAGGTTGGAATGAACGCTCCTTCCACGCTCCAGCGTGCTGGTATCCTGTAGCGCGGATGGGTTGAGGGGCATGCATGGACTGAACGTTCCTTCCACGTTCAGCGTGCCGCATTCCGCAAAGGAAACGTGAGAGGGGATAGTTCCAAGCTGGAATGAACGTTCCGTCCACGGC

>NZ_CP017172|20|3|9408211-9408660|CRT
GGTGGAATCAGCGTTCGTTCCACTGC	GTGCAGATGCGCTGCGGTGAACGCTGCCA
GTTGGAATGAACGTTCCGTCCGCAGC	CTGCGGTTACGGCAGAGTGGGGCCTGCATCTG
ACTGGATTGAACGTTCCTTTCACTGC	CTGCTGCTGCGGTCGGGCTCACCGTCTCAA
GCTGGAATGAACGTTCCGTCCACTGC	TCAAGGCCGCGAGCGAGGTGCTCACTCCTG
GCTGGAATGAACGTTCCGTCCACTGC	TCAAGGCCGTAGGGTGGAGTGCTCATCCAG
GTTGGAATGAACGCTCCTTCCACGCT	CCAGCGTGCTGGTATCCTGTAGCGCGGATGGGTTGAGGGGCATG
CATGGACTGAACGTTCCTTCCACGTT	CAGCGTGCCGCATTCCGCAAAGGAAACGTGAGAGGGGATAGTTCCAA
GCTGGAATGAACGTTCCGTCCACGGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017172.1\|WP_140796254.1\|9392110_9392563_-\|bactofilin-BacM	unknown	unknown	gnl\|CDD\|377376
NZ_CP017172.1\|WP_140878160.1\|9402662_9403412_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140878172.1\|9416440_9417682_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|377474
NZ_CP017172.1\|WP_140796256.1\|9393482_9394274_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|379293
NZ_CP017172.1\|WP_140796267.1\|9418862_9419249_+\|DoxX-family-protein	unknown	unknown	gnl\|CDD\|379266
NZ_CP017172.1\|WP_140878154.1\|9391562_9392108_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140878164.1\|9406854_9408105_+\|Bcr/CflA-family-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|340878
NZ_CP017172.1\|WP_140800557.1\|9413503_9415468_+\|signal-peptide-peptidase-SppA	unknown	unknown	gnl\|CDD\|273226
NZ_CP017172.1\|WP_140800552.1\|9403499_9404153_-\|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG	unknown	unknown	gnl\|CDD\|234637
NZ_CP017172.1\|WP_011557403.1\|9418081_9418408_+\|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|238042
NZ_CP017172.1\|WP_174259025.1\|9419309_9419915_-\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|99749
NZ_CP017172.1\|WP_140878152.1\|9389970_9390996_+\|L-histidine-N(alpha)-methyltransferase	unknown	unknown	gnl\|CDD\|378355
NZ_CP017172.1\|WP_140878170.1\|9415552_9416146_-\|cysteine-dioxygenase	unknown	unknown	gnl\|CDD\|380416
NZ_CP017172.1\|WP_140878168.1\|9410625_9413487_-\|insulinase-family-protein	unknown	unknown	gnl\|CDD\|223685
NZ_CP017172.1\|WP_140878166.1\|9408850_9409630_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP017172.1\|WP_140878156.1\|9392566_9393457_-\|ParB/RepB/Spo0J-family-partition-protein	unknown	unknown	gnl\|CDD\|275105
NZ_CP017172.1\|WP_140800556.1\|9409805_9410555_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP017172.1\|WP_140878162.1\|9404251_9406099_-\|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	unknown	unknown	gnl\|CDD\|235362
NZ_CP017172.1\|WP_140796266.1\|9418404_9418845_+\|SRPBCC-domain-containing-protein	unknown	unknown	gnl\|CDD\|176856
NZ_CP017172.1\|WP_140796252.1\|9391062_9391263_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP017172.1\|WP_140796254.1\|9392110_9392563_-\|bactofilin-BacM	gnl\|CDD\|377376	pfam04519, Bactofilin, Polymer-forming cytoskeletal. This is a family of bactofilins, a functionally diverse class of cytoskeletal, polymer-forming, proteins that is widely conserved among bacteria. In the example species C. crescentus, two bactofilins assemble into a membrane-associated laminar structure that shows cell-cycle-dependent polar localization and acts as a platform for the recruitment of a cell wall biosynthetic enzyme involved in polar morphogenesis. Bactofilins display distinct subcellular distributions and dynamics in different bacterial species, suggesting that they are versatile structural elements that have adopted a range of different cellular functions.	1.01311e-30
NZ_CP017172.1\|WP_140796256.1\|9393482_9394274_-\|AAA-family-ATPase	gnl\|CDD\|379293	pfam13614, AAA_31, AAA domain. This family includes a wide variety of AAA domains including some that have lost essential nucleotide binding residues in the P-loop.	6.16066e-92
NZ_CP017172.1\|WP_140796267.1\|9418862_9419249_+\|DoxX-family-protein	gnl\|CDD\|379266	pfam13564, DoxX_2, DoxX-like family. This family of uncharacterized proteins are related to DoxX pfam07681.	0.00582926
NZ_CP017172.1\|WP_140800552.1\|9403499_9404153_-\|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG	gnl\|CDD\|234637	PRK00107, gidB, 16S rRNA (guanine(527)-N(7))-methyltransferase RsmG.	5.12638e-59
NZ_CP017172.1\|WP_140878164.1\|9406854_9408105_+\|Bcr/CflA-family-efflux-MFS-transporter	gnl\|CDD\|340878	cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	8.01992e-100
NZ_CP017172.1\|WP_140800557.1\|9413503_9415468_+\|signal-peptide-peptidase-SppA	gnl\|CDD\|273226	TIGR00705, Protease_4, signal peptide peptidase SppA, 67K type. This model represents the signal peptide peptidase A (SppA, protease IV) as found in E. coli, Treponema pallidum, Mycobacterium leprae, and several other species, in which it has a molecular mass around 67 kDa and a duplication such that the N-terminal half shares extensive homology with the C-terminal half. This enzyme was shown in E. coli to form homotetramers. E. coli SohB, which is most closely homologous to the C-terminal duplication of SppA, is predicted to perform a similar function of small peptide degradation, but in the periplasm. Many prokaryotes have a single SppA/SohB homolog that may perform the function of either or both. [Protein fate, Degradation of proteins, peptides, and glycopeptides].	3.0814e-96
NZ_CP017172.1\|WP_140878166.1\|9408850_9409630_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	5.97827e-24
NZ_CP017172.1\|WP_011557403.1\|9418081_9418408_+\|winged-helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	1.0383e-18
NZ_CP017172.1\|WP_174259025.1\|9419309_9419915_-\|Uma2-family-endonuclease	gnl\|CDD\|99749	cd06260, DUF820, Domain of unknown function (DUF820). This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. They have been predicted to belong to the PD-(D/E)xK superfamily of nucleases.	7.0981e-30
NZ_CP017172.1\|WP_140878152.1\|9389970_9390996_+\|L-histidine-N(alpha)-methyltransferase	gnl\|CDD\|378355	pfam10017, Methyltransf_33, Histidine-specific methyltransferase, SAM-dependent. The mycobacterial members of this family are expressed from part of the ergothioneine biosynthetic gene cluster. EGTD is the histidine methyltransferase that transfers three methyl groups to the alpha-amino moiety of histidine, in the first stage of the production of this histidine betaine derivative that carries a thiol group attached to the C2 atom of an imidazole ring.	1.45183e-159
NZ_CP017172.1\|WP_140878170.1\|9415552_9416146_-\|cysteine-dioxygenase	gnl\|CDD\|380416	cd10548, cupin_CDO, cysteine dioxygenase, cupin domain. This family contains cysteine dioxygenase (CDO; EC 1.13.11.20), which catalyzes the conversion of cysteine to cysteine sulfinic acid, the first step in the biosynthesis of essential oxidized cysteine metabolites such as sulfate, hypotaurine, and taurine. CDO also plays an important role in the regulation of intracellular cysteine levels in mammals; CDO expression is altered in cancer cells, and abnormal or deficient CDO activity has been linked to Parkinson's disease, Alzheimer's disease, and rheumatoid arthritis. CDO is an iron-dependent thiol dioxygenase that uses molecular oxygen to oxidize the sulfhydryl group of cysteine to generate cysteine sulfinic acid. The CDO active site contains an amino acid-derived cofactor. These enzymes are found in prokaryotes as well as eukaryotes and belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	9.39167e-27
NZ_CP017172.1\|WP_140878168.1\|9410625_9413487_-\|insulinase-family-protein	gnl\|CDD\|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	8.03383e-69
NZ_CP017172.1\|WP_140878156.1\|9392566_9393457_-\|ParB/RepB/Spo0J-family-partition-protein	gnl\|CDD\|275105	TIGR04285, parB-like_partition_protein, nucleoid occlusion protein. This model describes nucleoid occlusion protein, a close homolog to ParB chromosome partitioning proteins including Spo0J in Bacillus subtilis. Its gene often is located near the gene for the Spo0J ortholog. This protein bind a specific DNA sequence and blocks cytokinesis from happening until chromosome segregation is complete.	9.30339e-83
NZ_CP017172.1\|WP_140878162.1\|9404251_9406099_-\|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	gnl\|CDD\|235362	PRK05192, PRK05192, tRNA uridine-5-carboxymethylaminomethyl(34) synthesis enzyme MnmG.	0
NZ_CP017172.1\|WP_140796266.1\|9418404_9418845_+\|SRPBCC-domain-containing-protein	gnl\|CDD\|176856	cd07814, SRPBCC_CalC_Aha1-like, Putative hydrophobic ligand-binding SRPBCC domain of Micromonospora echinospora CalC, human Aha1, and related proteins. This family includes the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of Micromonospora echinospora CalC, human Aha1, and related proteins. Proteins in this group belong to the SRPBCC domain superfamily of proteins, which bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket. MeCalC confers resistance to the enediyne, calicheamicin gamma 1 (CLM), by a self sacrificing mechanism which results in inactivation of both CalC and the highly reactive diradical enediyne species. MeCalC can also inactivate two other enediynes, shishijimicin and namenamicin. A crucial Gly of the MeCalC CLM resistance mechanism is not conserved in this subgroup. This family also includes the C-terminal, Bet v1-like domain of Aha1, one of several co-chaperones, which regulate the dimeric chaperone Hsp90. Aha1 promotes dimerization of the N-terminal domains of Hsp90, and stimulates its low intrinsic ATPase activity, and may regulate the dwell time of Hsp90 with client proteins. Aha1 can act as either a positive or negative regulator of chaperone-dependent activation, depending on the client protein, but the mechanisms by which these opposing functions are achieved are unclear. Aha1 is upregulated in a number of tumor lines co-incident with the activation of several signaling kinases.	1.15112e-27
NZ_CP017172.1\|WP_140878172.1\|9416440_9417682_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|377474	pfam05157, T2SSE_N, Type II secretion system (T2SS), protein E, N-terminal domain. This domain is found at the N-terminus of members of the Type II secretion system protein E. Proteins in this subfamily are typically involved in Type 4 pilus biogenesis, though some are involved in other processes; for instance aggregation in Myxococcus xanthus. The structure of this domain is now known.	2.05983e-17

>NZ_CP017172.1|WP_140878164.1|9406854_9408105_+|Bcr/CflA-family-efflux-MFS-transporter
MTTPSTKPTEKGTLGLELLLGTLTAFAPLSIDMYLPALPRIAEDLQSTAPAIQLTLASCFAGLALGQLFTGPLIDRFGRTRPLYAGLALYVLGSLGCALAPSASMLVAMRFVQALGGSVALVVPRAVVRDLWSGANAARTMSRLMLVMGVAPILAPLLGGLVLQYSGWRAIFVVLAAVGAVALACVLKSLPETAPPHVGSQSMLSRMGALMKDPDFVGPALAGGFAQAGMFAYIAGSPFVFISLYGIPEEHFGWFFGVNAMGLIAVAQLNRKLVTHLPLHRLLRLALSLCVVTAVAVLAVAWTGFMGLWGIAVTLFFFVSAMGLVGPNAAAIALERHAARAGMASAALGALQFTAAAGASWAVSTFNNGTAMPMAGVMAAMALLAWLAAFFGLRARTRQQGAGELGGGVASRQGAS
>NZ_CP017172.1|WP_140878162.1|9404251_9406099_-|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG
MGLRYDVIVVGLGHAGSEAALACARMGLATLGLTLKRERSAVLSCNPAVGGTAKGHLVRELDALGGEMGRAADKVGTHFKTLNASKGPAVQASRLLCDRDAYAAGMQAVLFSQPNLTVREGEVAALVAGGGRVEGVVLGDGTQVSASAVLLTTGTFLQALMHVGEQKEVGGRLGDDAARGLSESLRALGFTLGRFKTGTPARLARASIDWDALEPQPGDTRVRPFSWRTQVEGEGGMPFPRQPSVTCALTATTPRTHAVLRDNLHRSPLFQGDIVGRGPRYCPSLEDKVVRFASREKHQVFLEPEGPTSPLVYPAGLSTSLPADVQLTFLRTIPGLEQVEVVRFGYAVEYDYAPPTQLKATLETKAIAGLYFAGQLNGTSGYEEAAFQGLWAGINAALQMKGEPPLLPGRDEAHGAVLVDDLVTKGVEEPFRMFTSRSEHRLKLREGNADLRLARHGHRVGLLPREALERAEARGRAVTEEVARLKRTGLAARLRRPEVTYAQLGEGREDWPVLSPDVAEEVEVEVKYEGYVAQAARAAAREAESTDRWRIPEGYRFHEVRGLSSEAVEKLTAHRPGTVGQARRIPGLTPAAVSLLLVALKRGAGAPTVCSQPED
>NZ_CP017172.1|WP_140800552.1|9403499_9404153_-|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG
MDNARFEDQLAAGCRALGVTVAADLGPRLQRLMSELLKWNAKVNLTAITAPEEVLEKHFLDSLAVLPEVTGAATLLDLGAGAGFPGLPLKLALPALGVTLVDTVGKKVAFIKAAAASLGLQGVRGLHARAEGQPETEGIPRAEVLIARAFMDLPDWLALAPAYVEPGGRVVAMLGKAQTDAELAARAAERQLRVVSARAYRLPFSGAERQVAVFAKE
>NZ_CP017172.1|WP_140878160.1|9402662_9403412_-|hypothetical-protein
MLSDFSGAHPTGREGWREPGASLGFTAEVPRMKPLPMDRPRVWLFERHAHAVTLKASRSSFERQWGPPHLVVTRDDGRFLEAHWGWRSECGLELVVVSLREADRFHVFIEPLEVDHAMAHLGLKDEVVEWRADAGLPLLREGWAVTRMDETGNRYDIALSPERAHVACFARILEERAHKQSYYVEFRGTPAPGEPARKDWAVIRQDEHGNRAEVARLQSEQGAHAFADAYEADPRHKQTYFVEPVAPRS
>NZ_CP017172.1|WP_140796256.1|9393482_9394274_-|AAA-family-ATPase
MGRIICISNQKGGVGKTTTAINLAASLASAERRTLLVDMDPQGNAGSGLGIKQDNITGTIYEALLNDRPIKELLHPTELRYLQVVPATPDLTGAEVELVNQDNREFRLRDALRPLAPEYDYIIIDCPPSLGLLTLNALAAADSVLIPLQCEYYALEGLSQLTHTIDLVKQGLNPDLKMEGILLTMFDSRANIAHQVVEEVRGYFKKQVFEVIVPRNVRLSECPSFGKPIILYDIKSKGCESYLALGRELMKRDTPKSPRRRVA
>NZ_CP017172.1|WP_140878156.1|9392566_9393457_-|ParB/RepB/Spo0J-family-partition-protein
MVKADMQKRALGRGLSALIPQAGATSSGKGEQAPKAGVLKLPIESIHRDKDQPRTYFDEEKLKELSDSIKAQGVLQPILVRKDGDGYRIIAGERRWRASQAAGLKEVPAIVRDVTEVQAFELALVENLQRADLNPIEEAEGYKRLVEEFKLTQEQVSARVGKERSTVANALRLLALPSDVKGMVADGSLSMGHARALLGVPRLPELQNLAKQVADKKLSVRDTERLVQQSRTSGKKDAGKAAPKQSPQVKSLVEELQRRLGTKVRLTERSPGKGTIEVDFFSYDDLDRLLKLLRKE
>NZ_CP017172.1|WP_140796254.1|9392110_9392563_-|bactofilin-BacM
MALLGGKKDEASSKPLFRREEESVSQRSGEVHTLLGKGSEFEGKLTFEGQVRIDGKFQGQIITKDVLVIGDGAKVQAEIQAGTVIINGQVEGNVKATQIIELKTPGRVKGNLETPSLSMDRGVIFEGSLKMENLGTAGARPPPPPGGEKK
>NZ_CP017172.1|WP_140878154.1|9391562_9392108_-|hypothetical-protein
MRSWKHMAPASLLALTLLGGCKGCGQEDAASGTGEDDGRPSSIRSGVKVPLPDGWSALVAPDESFQAGPPGRPVLRVDLRRGDGEQLPSVDTLADRVREELKDFELSLDQEEETERYSLLRITLAPKLADGGVGPEAPGFFGARRVGNDLFLCASLPGASAEDVLRATEACREIQVQGSLP
>NZ_CP017172.1|WP_140796252.1|9391062_9391263_-|hypothetical-protein
MSFSGMLPLQLATVDIAPVGEQLIAVGGLVVAGLGALWAAWTRPSAQPVPVPIPVRGGSSRRNPRR
>NZ_CP017172.1|WP_140878152.1|9389970_9390996_+|L-histidine-N(alpha)-methyltransferase
MRVTTVPTVATPGEDAQHTPGVQVDVYVKPGDAKRALREEALQGLCGTPKELSPKWLYDERGSQLFDDITRLPEYYPTRREREILLAHAGDIARLSGADTLIELGSGTSEKTRLLLDALEEAGRLARFVPFDVSEAFLRRAASGLAREYPGITVHAVVGDFERHLGQLPNGGRRLVAFLGGTIGNLKPAQRALFLRQLSAGLQPGDGLLLGTDLIKDRERLYAAYNDSAGVTAAFNRNVLKVLNRELGGDFDPDAFEHFAPFDEKNAWIEMRLVSRREQTVWLSTLRKQVDFTEGEVLRTEVSCKFHQQQVASELSAAGLTLAEWWTDAAGDFALSLAFKR
>NZ_CP017172.1|WP_140878166.1|9408850_9409630_+|alpha/beta-fold-hydrolase
MTSTSRTVQGPTGQLAVTDTGSGGLPIVFVHSNASRREQWAAQQAHLKQRTVSFDLRGMGDSGLDAQGRYGAEDMASDIHAVATALDLERFVLVGHSFGGYVAAEYARGWPERLAGLVIVDAAGTMPPLPSEQLQGFHEGTRPESYRAFMDAWFTPILQNAKPHTHESVMRWLHATPREVVVGALESMLTFNSDRVMERYKGPLHTLVVDAFIQPNAYHLLYPGTPHTVFSDVSHWLMMDAPERVNAALDAFLATLPPR
>NZ_CP017172.1|WP_140800556.1|9409805_9410555_+|hypothetical-protein
MRRLRRTCFALGISFVVTGCTTTLYKPNQISAPLLREEGELKGTLGNNNLQVAWSPREGVGLLAQGYYERYAEGERRANGALGEVGGGLYGTFLGNAVWEAYGGLGYGQSTASDRLEANGAMPRDVGFTARAVRAFIQPNLGYVTPYFELAGSVRLSAVKYVSLDANGYTDAERSREFLVADDVTRPVWLFAEPAVTVKGGYKWVKVYAQRAWALKLGGKPLPHERDSTVVGLSVDVASWYHDFQWGSR
>NZ_CP017172.1|WP_140878168.1|9410625_9413487_-|insulinase-family-protein
MHSQTTREDRMKRRTPLSLVAALMMVAGTPVWAQTPAAANKAPATQSAVTQNKAKGRVLAPVTSVEGISEYRLPNGLKVLLFPDPTKPTVTVNVTYFVGSKHEGYGETGMAHLLEHLMFKGTPTTRNVPQALTERGARPNGTTWLDRTNYYETLPASDANLRWALSFEADRMVNSFIAKKDLDSEMTVVRNEFESGENDPRGILFERVMSAAYIWHSYGKSTIGARSDLENVPIDRLQAFYRKYYRPDNAMLVVAGRFDEAKALSMIQDTFGKLKKPGLPLPATYTAEPTQDGEREVQLRRVGDTALLTSLYHVPEGAHPDFAAIDVLTLVMGNNPSGRLYKSMVETKKASRVSASNLQLRDPGIIVFSAEMRDDQPVAAAREALLKTVEDASRTPFTEEEVNRAKATLSKYIDLTINNSERVAINLSEWEATGDWRLLFLHRDRIEAVTTEDVTRVAAAYLKSSNRTLGTFIPTPKPDRAELPAPVDVATMMEGFKGRDAVAQGEAFDPSPANIESRVQRGELPGGVKYAVLPKKTRGNMVNVSLTLRWGTEEALRGKSDAAQYAGRMLMRGTKKRTRQQLQDAFDKLKARVGVDGSSTGVSASIECPRDSLPEVLKLVAEVLREPSFDEKEFAMLKQERLASLESERSEPQTLGNIAFWRSLSGHYLKGHPYYVATLDERIAGVKDTTLEQARAFHKAFYGASNGELAVVGDFESKDIVALAGTLLGDWKSPAPYQRVQQVFGGGESASVALETPDKANAYYMAGQSLKLRKDDKDWPALVLGNFVLGGGFLNSRLATRIRQQDGLSYGVASSLDASDVDEVGTFFTYAIYAPENAARLETAMREEVTRAVQKGYSAEELQKARTGILEYRQSARAQDGSLARQLASYLFLGRTLAFDAALEQKLTQLKPEDVRKAMERHLDWTKVTQVRAGDFATAQKKAAPPAKVPAAP
>NZ_CP017172.1|WP_140800557.1|9413503_9415468_+|signal-peptide-peptidase-SppA
MSPGPSRTVALRATRRRGRTVTQGKHGDAQASSPARVSSKHPLPGPYPVSPGHQESLRMKRFFIGALAFVGALSVLFVVGLVGLMLLASASKPGVPSNLVLELDLEDPLSEHGGGDSLVGAFGEEPTTVRDVVEALEKAGDDARVKSLLVRIGHPGTPAATQELRDAVKAFRAKGKKAVAYSDTFGELGNSTLGYYLASAFDEIYIQPSGDVNINGLAFELPFAREAFAKLGVTPHYFARYEYKNAINSYTEQDYTAPHREATEGFTNSLFGQIVRGIAADRGLTEDVVRGLIDKAPLMAQEAVEAKLVTGLRYRDEVLGGLKEQAGEGARFLYVKKYLERAGRPNVSGNTIALVYGVGEVMRGKNQSNPLSGGQSMGAESVAAALRKATEDSRVKAIVFRVDSPGGSYVASDTVRREVQRAKEAGKPVIVTMGSYAASGGYFVAMEADRIVAHPGTLTGSIGVYAGKFVTAGFWEKLGVNFDSVAVGKNAEMFGSDADYTPEQQARMDASLDRIYADFTTRAAASRKLPLEKLQSLAKGRVWTGEDALEHGLVDALGGYPKALELAKEAAKLPADARVNVEVYPRKKPASAVLSELLGQTGDNSEDDAASISVLSPWTTLVAGVRKVYAVGARMGLFEGTRGELYAPLPEASW
>NZ_CP017172.1|WP_140878170.1|9415552_9416146_-|cysteine-dioxygenase
MNAMCLGEWVELLREKAGGMPGLEGVGEGLAGLVLEPASLQPYLHFRRGRYTRNLIYRDARLEVLLNCWDAGTFSPIHDHDGQECWFSVQSGGFVLENYTLEAGGLGPGPARLGPPVMVGPVGAGFVDFRCPEAPIHRVTAARGPAVSLHVYAGPVDRCLVFDTRRQRCVSRELRYHSMFGRPLTQLPDVPQPPASF
>NZ_CP017172.1|WP_140878172.1|9416440_9417682_+|general-secretion-pathway-protein-GspE
MKKRLGDILLERGVVDALQLHSALAYQRKWGVPLGQVVVDQRFSTAQQVLEALAFQAGMQTVDLDVQPPDASLTWLIPERVAEAHRVVPLKLEGQGGRDSVLVVAIAAPASLASLDAVKSVSGKPRVVAKLASDAAIRRAIGRLYRGETGDAAPRRAGMESFSLPEADERMPMVLGGSMAELTNMEAPGGEDGLPLLGSLEEVVVQAQAVPAEMRRLVQAIRAMPEPLAAVAQPLPLEAGRSEQAATPATTEGLHLAHVSRPGSTKAPFSARAMQLTVGTRNHVPTALPMLTAAQPVPMAQVLVYGWGEEATTGLVRVMSEAGLRAQVASTEELLAANAAQVVVAPLPSMEALPRQVHAQVLVAGKMPEQDLPRAQAVGARGFLAAPVDPDLLLRAVRRLARPAGDADLKRAS
>NZ_CP017172.1|WP_011557403.1|9418081_9418408_+|winged-helix-turn-helix-transcriptional-regulator
MMHTEPGVFGAISHPARRRMLDLLVDGDRPVNSIAENFEMSRPAVSQHLRVLLDAGLVTEQRHGRERRYRLVPERLEPVRDWIAHYERFWDDNFARLRRHLEKGDKQQ
>NZ_CP017172.1|WP_140796266.1|9418404_9418845_+|SRPBCC-domain-containing-protein
MTTKTIRRELKFTQSPAVVWRALATSEALADWMYPNDFEPRVGHRFTFRVPPDPRAQFDGLVVQCEVLRCAPPSELEFTWVVGEGWLDTRVSYRLEADGDGTRVLFEHSGFKEDQAFHGAEYGWKMMHGKLAKTLEKASDNPALKA
>NZ_CP017172.1|WP_140796267.1|9418862_9419249_+|DoxX-family-protein
MNIVFWILQAVLALLFLAGGSYKAFSFQQLASQFSEVPLGAWRALGFLEMAGGVLLIIPAAFKWMPSLTAHAAAVLTFETFALAVLYARHSTKMTPENPMLWSLVMGVLIAFVAYGRYILNPVVAAAA
>NZ_CP017172.1|WP_174259025.1|9419309_9419915_-|Uma2-family-endonuclease
MIEGIIPLANHSMLSALPSGWVGEILDEELVASPRPTAAQTRAAFMLGVELGEQLDKRRGGSGRWCFLRAPELHLGHDMLVPDMAGWRRERVDVPFEPDVPFLTLVPDWVCEVLTPSTAALDRARKLPLYARAGVSHVWLVDPAARTLEVYQRVKRGWLLTGSYEDDSLVRADPFPSSTLELGSLWLPEGSEKPSLLAAVP

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP017172_19	19.130\|8882655\|38\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8882655-8882692	38	NZ_CP017172.1	8570975-8571012	0	1.0
NZ_CP017172_7	7.1\|3414411\|30\|NZ_CP017172\|CRT	3414411-3414440	30	NZ_CP017172.1	3414363-3414392	1	0.967
NZ_CP017172_19	19.30\|8875568\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875568-8875602	35	NZ_CP017172.1	4324233-4324267	1	0.971
NZ_CP017172_14	14.3\|7202099\|19\|NZ_CP017172\|CRISPRCasFinder	7202099-7202117	19	NZ_CP017172.1	84050-84068	2	0.895
NZ_CP017172_19	19.18\|8874719\|35\|NZ_CP017172\|CRISPRCasFinder,CRT	8874719-8874753	35	NZ_CP017172.1	4328357-4328391	2	0.943

1. spacer 19.130|8882655|38|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to position: 8570975-8571012, mismatch: 0, identity: 1.0

ccatggtggaccgcatctacgcggcgttcgacaccatg	CRISPR spacer
ccatggtggaccgcatctacgcggcgttcgacaccatg	Protospacer
**************************************

2. spacer 7.1|3414411|30|NZ_CP017172|CRT matches to position: 3414363-3414392, mismatch: 1, identity: 0.967

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

3. spacer 19.30|8875568|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to position: 4324233-4324267, mismatch: 1, identity: 0.971

cggatgccgtccaagtcacaccgggccgcgagcgc	CRISPR spacer
cggatgccgtccaagtcacaccgcgccgcgagcgc	Protospacer
*********************** ***********

4. spacer 14.3|7202099|19|NZ_CP017172|CRISPRCasFinder matches to position: 84050-84068, mismatch: 2, identity: 0.895

gagccgccgtcgctgccac	CRISPR spacer
gagccaccgccgctgccac	Protospacer
*****.***.*********

5. spacer 19.18|8874719|35|NZ_CP017172|CRISPRCasFinder,CRT matches to position: 4328357-4328391, mismatch: 2, identity: 0.943

gcctccgggtccgcgcgcttcgcgttgtgcgagag	CRISPR spacer
gcctccgggtctgcgcgcttggcgttgtgcgagag	Protospacer
***********.******** **************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NC_003085	Myxococcus phage Mx8, complete genome	42771-42802	2	0.938
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	AF396866	Bacteriophage Mx8, complete genome	42771-42802	2	0.938
NZ_CP017172_14	14.1\|7201994\|25\|NZ_CP017172\|CRISPRCasFinder	7201994-7202018	25	NZ_CP017242	Rhizobium etli 8C-3 plasmid pRsp8C3a, complete sequence	283294-283318	3	0.88
NZ_CP017172_14	14.1\|7201994\|25\|NZ_CP017172\|CRISPRCasFinder	7201994-7202018	25	NZ_CP035001	Rhizobium acidisoli strain FH23 plasmid pRapFH23c, complete sequence	579957-579981	3	0.88
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP054620	Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence	413240-413264	3	0.88
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP032685	Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence	793485-793509	3	0.88
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP032690	Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence	793034-793058	3	0.88
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP028919	Gemmobacter sp. HYN0069 plasmid unnamed1, complete sequence	268476-268500	3	0.88
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP021355	Rhodococcus sp. S2-17 plasmid pRB98, complete sequence	804331-804362	4	0.875
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	CP003957	Rhodococcus opacus PD630 plasmid 8, complete sequence	37644-37675	4	0.875
NZ_CP017172_14	14.1\|7201994\|25\|NZ_CP017172\|CRISPRCasFinder	7201994-7202018	25	NZ_CP011665	Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence	353951-353975	4	0.84
NZ_CP017172_14	14.1\|7201994\|25\|NZ_CP017172\|CRISPRCasFinder	7201994-7202018	25	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	416444-416468	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_AP021845	Azospira sp. I09 plasmid pAZI09, complete sequence	147002-147026	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1127267-1127291	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP020399	Burkholderia multivorans strain FDAARGOS_246 plasmid unnamed, complete sequence	523036-523060	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	87057-87081	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP041653	Streptomyces sp. RLB1-9 plasmid pRLB1-9.1, complete sequence	99278-99302	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	768559-768583	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_AP012556	Mycobacterium avium subsp. hominissuis TH135 plasmid pMAH135, complete sequence	15191-15215	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP007792	Corynebacterium marinum DSM 44953 plasmid pCmarinum1, complete sequence	29311-29335	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NC_014755	Sulfuricurvum kujiense DSM 16994 plasmid pSULKU02, complete sequence	9023-9047	4	0.84
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	282455-282479	4	0.84
NZ_CP017172_5	5.1\|1398094\|25\|NZ_CP017172\|CRISPRCasFinder	1398094-1398118	25	NZ_CP029211	Aquabacterium olei strain NBRC 110486 plasmid pTB101, complete sequence	63439-63463	5	0.8
NZ_CP017172_14	14.4\|7202141\|25\|NZ_CP017172\|CRISPRCasFinder	7202141-7202165	25	NZ_CP021830	Sinorhizobium meliloti strain HM006 plasmid psymA, complete sequence	1279267-1279291	5	0.8
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1503853-1503880	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	84950-84977	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1576510-1576537	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1582321-1582348	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1880310-1880337	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1501145-1501172	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	398009-398036	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1583961-1583988	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	1293609-1293636	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1510199-1510226	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	1541873-1541900	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1506932-1506959	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1506437-1506464	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1595441-1595468	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1593842-1593869	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1496049-1496076	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1593842-1593869	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1496695-1496722	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1593842-1593869	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1593842-1593869	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1593842-1593869	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1496071-1496098	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1501551-1501578	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1482201-1482228	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1535148-1535175	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1574347-1574374	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1591157-1591184	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1496071-1496098	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1496071-1496098	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1496071-1496098	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1593845-1593872	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1129772-1129799	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	566702-566729	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	434516-434543	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1161498-1161525	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	888091-888118	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	796407-796434	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	1533362-1533389	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	796407-796434	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	796408-796435	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	457326-457353	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	796404-796431	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	451381-451408	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	796410-796437	5	0.821
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	451381-451408	5	0.821
NZ_CP017172_19	19.15\|8874508\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874508-8874539	32	MH651167	Gordonia phage Angelique, complete genome	33317-33348	5	0.844
NZ_CP017172_19	19.15\|8874508\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874508-8874539	32	MT952844	Gordonia phage Bosnia, complete genome	36305-36336	5	0.844
NZ_CP017172_19	19.112\|8881386\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881386-8881417	32	NZ_CP020568	Kitasatospora aureofaciens strain DM-1 plasmid unnamed1, complete sequence	235815-235846	5	0.844
NZ_CP017172_20	20.1\|9408237\|29\|NZ_CP017172\|CRT	9408237-9408265	29	NZ_CP040720	Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence	159040-159068	5	0.828
NZ_CP017172_20	20.1\|9408237\|29\|NZ_CP017172\|CRT	9408237-9408265	29	NZ_CP018759	Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence	60570-60598	5	0.828
NZ_CP017172_7	7.1\|3414411\|30\|NZ_CP017172\|CRT	3414411-3414440	30	MN119376	Streptomyces phage Geostin, complete genome	28793-28822	6	0.8
NZ_CP017172_7	7.1\|3414411\|30\|NZ_CP017172\|CRT	3414411-3414440	30	MH155868	Streptomyces phage FlowerPower, complete genome	28793-28822	6	0.8
NZ_CP017172_7	7.1\|3414411\|30\|NZ_CP017172\|CRT	3414411-3414440	30	MN284894	Streptomyces phage Fabian, complete genome	28793-28822	6	0.8
NZ_CP017172_7	7.3\|3414516\|30\|NZ_CP017172\|CRT	3414516-3414545	30	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	15099-15128	6	0.8
NZ_CP017172_7	7.3\|3414516\|30\|NZ_CP017172\|CRT	3414516-3414545	30	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	362521-362550	6	0.8
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_AP014706	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence	155353-155384	6	0.812
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1160061-1160088	6	0.786
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1613187-1613214	6	0.786
NZ_CP017172_19	19.13\|8874363\|34\|NZ_CP017172\|CRISPRCasFinder,CRT	8874363-8874396	34	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	522649-522682	6	0.824
NZ_CP017172_19	19.15\|8874508\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874508-8874539	32	MT521999	Gordonia Phage Jablanski, complete genome	33674-33705	6	0.812
NZ_CP017172_19	19.42\|8876418\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876418-8876449	32	NZ_CP033971	Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed2, complete sequence	80256-80287	6	0.812
NZ_CP017172_19	19.120\|8881949\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881949-8881981	33	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	324439-324471	6	0.818
NZ_CP017172_19	19.120\|8881949\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881949-8881981	33	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	327425-327457	6	0.818
NZ_CP017172_19	19.120\|8881949\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881949-8881981	33	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	373733-373765	6	0.818
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_AP014706	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence	168109-168140	7	0.781
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_AP014706	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence	377010-377041	7	0.781
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	119509-119540	7	0.781
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP015090	Pelagibaca abyssi strain JLT2014 plasmid pPABY2, complete sequence	118113-118144	7	0.781
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP007453	Peptoclostridium acidaminophilum DSM 3953 strain al-2 plasmid EAL2_808p, complete sequence	104690-104721	7	0.781
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	AM261282	Uncultured bacterium IncP-1 plasmid pKJK5 complete sequence	7056-7083	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_CP028340	Thauera aromatica K172 plasmid pKJK172, complete sequence	6277-6304	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	KC964605	Uncultured bacterium plasmid pMLUA1, complete sequence	7055-7082	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	KC964606	Uncultured bacterium plasmid pMLUA3, complete sequence	7055-7082	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	KC964607	Uncultured bacterium plasmid pMLUA4, complete sequence	7055-7082	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_MN366356	Bacterium plasmid pALTS27, complete sequence	5741-5768	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	NZ_MN366360	Bacterium plasmid pALTS32, complete sequence	5741-5768	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	JQ004406	Uncultured bacterium plasmid pHH128, complete sequence	11731-11758	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	JQ004407	Uncultured bacterium plasmid pHH3408, complete sequence	11733-11760	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	JQ004408	Uncultured bacterium plasmid pHH3414, complete sequence	11733-11760	7	0.75
NZ_CP017172_14	14.6\|7202261\|28\|NZ_CP017172\|CRISPRCasFinder	7202261-7202288	28	JQ004409	Uncultured bacterium plasmid pKS77, complete sequence	11604-11631	7	0.75
NZ_CP017172_19	19.11\|8874225\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874225-8874257	33	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	208112-208144	7	0.788
NZ_CP017172_19	19.15\|8874508\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874508-8874539	32	NZ_CP006370	Aureimonas sp. AU20 plasmid pAU20c, complete sequence	275086-275117	7	0.781
NZ_CP017172_19	19.16\|8874577\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874577-8874608	32	MK494099	Mycobacterium phage Typha, complete genome	51673-51704	7	0.781
NZ_CP017172_19	19.16\|8874577\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874577-8874608	32	NZ_CP018385	Burkholderia pseudomallei strain 2008724860 plasmid p1, complete sequence	53169-53200	7	0.781
NZ_CP017172_19	19.22\|8875002\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8875002-8875033	32	NZ_CP010408	Streptomyces vietnamensis strain GIMV4.0001 plasmid pSVL1, complete sequence	117299-117330	7	0.781
NZ_CP017172_19	19.37\|8876066\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876066-8876097	32	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1226815-1226846	7	0.781
NZ_CP017172_19	19.49\|8876912\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876912-8876943	32	JQ768459	Pseudomonas phage Lu11, complete genome	61026-61057	7	0.781
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	NZ_CP039892	Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499c, complete sequence	6149-6181	7	0.788
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	MH178382	Streptomyces phage Salete, complete genome	33239-33271	7	0.788
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	MH178381	Streptomyces phage BayC, complete genome	33239-33271	7	0.788
NZ_CP017172_19	19.70\|8878401\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878401-8878433	33	NZ_CP039433	Rhodococcus sp. SGAir0479 plasmid unnamed	13729-13761	7	0.788
NZ_CP017172_19	19.78\|8878959\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878959-8878990	32	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	355612-355643	7	0.781
NZ_CP017172_19	19.81\|8879169\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879169-8879203	35	ASAB01000001	Pectobacterium atrosepticum CFBP 6276 plasmid pL1Pa6276, complete sequence, whole genome shotgun sequence	5472-5506	7	0.8
NZ_CP017172_19	19.92\|8879959\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879959-8879991	33	NZ_LR594663	Variovorax sp. RA8 plasmid 2	379299-379331	7	0.788
NZ_CP017172_20	20.3\|9408350\|30\|NZ_CP017172\|CRT	9408350-9408379	30	NZ_CP039919	Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626b, complete sequence	126035-126064	7	0.767
NZ_CP017172_20	20.3\|9408350\|30\|NZ_CP017172\|CRT	9408350-9408379	30	NC_008269	Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence	519088-519117	7	0.767
NZ_CP017172_3	3.1\|1043968\|31\|NZ_CP017172\|CRISPRCasFinder	1043968-1043998	31	NZ_CP025513	Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence	1097455-1097485	8	0.742
NZ_CP017172_3	3.1\|1043968\|31\|NZ_CP017172\|CRISPRCasFinder	1043968-1043998	31	MN310546	Microbacterium phage PhriedRice, complete genome	26649-26679	8	0.742
NZ_CP017172_3	3.1\|1043968\|31\|NZ_CP017172\|CRISPRCasFinder	1043968-1043998	31	MT310890	Microbacterium phage Phedro, complete genome	26545-26575	8	0.742
NZ_CP017172_3	3.1\|1043968\|31\|NZ_CP017172\|CRISPRCasFinder	1043968-1043998	31	MT310889	Microbacterium phage Phractured, complete genome	26545-26575	8	0.742
NZ_CP017172_3	3.1\|1043968\|31\|NZ_CP017172\|CRISPRCasFinder	1043968-1043998	31	MT310891	Microbacterium phage Pharky, complete genome	26545-26575	8	0.742
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	KJ538722	Mycobacterium phage HH92, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	KT222940	Mycobacterium phage Kinbote, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MH727549	Mycobacterium phage Gancho, complete genome	24221-24252	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MK919482	Mycobacterium phage DeepSoil15, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MT657330	Mycobacterium phage Webster2, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MF919517	Mycobacterium phage LilHazelnut, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	EU203571	Mycobacterium phage Giles, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MK494095	Mycobacterium phage Daegal, complete genome	24791-24822	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MT818421	Mycobacterium phage Luke, complete genome	24452-24483	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MH697577	Mycobacterium phage Amochick, complete genome	24503-24534	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MT684594	Mycobacterium phage Hadrien, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MT114159	Mycobacterium phage Ein37, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	KT246485	Mycobacterium phage OBUpride, complete genome	24491-24522	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	KT454972	Mycobacterium phage Evanesce, complete genome	24497-24528	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP021915	Sagittula sp. P11 plasmid unnamed2, complete sequence	116545-116576	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_LR594692	Variovorax sp. WDL1 plasmid 4	120417-120448	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NC_011368	Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG201, complete sequence	143210-143241	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP031599	Roseovarius indicus strain DSM 26383 plasmid pRIdsm_01, complete sequence	190664-190695	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP045373	Sulfitobacter sp. THAF37 plasmid pTHAF37_a, complete sequence	32053-32084	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	226010-226041	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP049732	Rhizobium leguminosarum strain A1 plasmid pRL11, complete sequence	101461-101492	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1417065-1417096	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	199701-199732	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP021805	Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence	1006311-1006342	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP021807	Sinorhizobium meliloti strain T073 plasmid accessoryA, complete sequence	38966-38997	8	0.75
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP045549	Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence	82560-82591	8	0.75
NZ_CP017172_19	19.11\|8874225\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874225-8874257	33	NC_015382	Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence	209996-210028	8	0.758
NZ_CP017172_19	19.11\|8874225\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874225-8874257	33	NZ_CP048642	Streptomyces aureoverticillatus strain HN6 plasmid unnamed, complete sequence	10874-10906	8	0.758
NZ_CP017172_19	19.11\|8874225\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874225-8874257	33	NZ_CP022418	Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-3, complete sequence	43110-43142	8	0.758
NZ_CP017172_19	19.16\|8874577\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874577-8874608	32	NZ_CP046254	Sphingobium sp. CAP-1 plasmid p1, complete sequence	89405-89436	8	0.75
NZ_CP017172_19	19.20\|8874861\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874861-8874893	33	NZ_CP021805	Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence	57661-57693	8	0.758
NZ_CP017172_19	19.27\|8875357\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875357-8875390	34	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	480283-480316	8	0.765
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP033968	Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed1, complete sequence	187737-187768	8	0.75
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP037902	Cupriavidus metallidurans strain BS1 plasmid p1, complete sequence	140410-140441	8	0.75
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	496032-496063	8	0.75
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3141094-3141125	8	0.75
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	551369-551400	8	0.75
NZ_CP017172_19	19.40\|8876275\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876275-8876306	32	NZ_CP030830	Neorhizobium sp. NCHU2750 plasmid pNCHU2750c, complete sequence	269305-269336	8	0.75
NZ_CP017172_19	19.40\|8876275\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876275-8876306	32	NC_023286	Streptomyces sp. F12 plasmid pFRL6, complete sequence	376854-376885	8	0.75
NZ_CP017172_19	19.40\|8876275\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876275-8876306	32	MN234195	Mycobacterium phage Xula, complete genome	18910-18941	8	0.75
NZ_CP017172_19	19.41\|8876344\|37\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876344-8876380	37	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	604491-604527	8	0.784
NZ_CP017172_19	19.42\|8876418\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876418-8876449	32	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	501990-502021	8	0.75
NZ_CP017172_19	19.47\|8876771\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876771-8876802	32	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	1178542-1178573	8	0.75
NZ_CP017172_19	19.49\|8876912\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876912-8876943	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	1939213-1939244	8	0.75
NZ_CP017172_19	19.54\|8877268\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877268-8877300	33	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	1757561-1757593	8	0.758
NZ_CP017172_19	19.55\|8877338\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877338-8877371	34	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	915745-915778	8	0.765
NZ_CP017172_19	19.55\|8877338\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877338-8877371	34	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	2281383-2281416	8	0.765
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NZ_CP020897	Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence	55430-55462	8	0.758
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_012854	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132505, complete sequence	223690-223722	8	0.758
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_007764	Rhizobium etli CFN 42 plasmid p42c, complete sequence	64486-64518	8	0.758
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_021907	Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1b, complete sequence	64371-64403	8	0.758
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	74057-74089	8	0.758
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_013858	Azospirillum sp. B510 plasmid pAB510d, complete sequence	221281-221313	8	0.758
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	KU530220	Streptomyces phage Xkcd426, complete genome	38857-38889	8	0.758
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	175856-175888	8	0.758
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	2053821-2053852	8	0.75
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1573483-1573514	8	0.75
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1165546-1165577	8	0.75
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NZ_CP053022	Sphingobium yanoikuyae strain YC-XJ2 plasmid p-A-Sy, complete sequence	203313-203344	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP015090	Pelagibaca abyssi strain JLT2014 plasmid pPABY2, complete sequence	164308-164339	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NC_012807	Methylorubrum extorquens AM1 plasmid p1META1, complete sequence	16877-16908	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	273729-273760	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP025014	Rhizobium leguminosarum strain Norway plasmid pRLN2, complete sequence	11548-11579	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	391099-391130	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP048282	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence	11454-11485	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP022566	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK02, complete sequence	287858-287889	8	0.75
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	183537-183568	8	0.75
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP039909	Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence	89866-89897	8	0.75
NZ_CP017172_19	19.119\|8881880\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881880-8881911	32	NC_015727	Cupriavidus necator N-1 plasmid pBB1, complete sequence	142124-142155	8	0.75
NZ_CP017172_19	19.119\|8881880\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881880-8881911	32	NZ_CP020810	Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed1, complete sequence	67974-68005	8	0.75
NZ_CP017172_19	19.120\|8881949\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881949-8881981	33	NZ_CP022365	Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence	175005-175037	8	0.758
NZ_CP017172_19	19.123\|8882160\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8882160-8882192	33	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	979671-979703	8	0.758
NZ_CP017172_7	7.3\|3414516\|30\|NZ_CP017172\|CRT	3414516-3414545	30	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	15078-15107	9	0.7
NZ_CP017172_7	7.3\|3414516\|30\|NZ_CP017172\|CRT	3414516-3414545	30	NZ_CP021083	Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence	229435-229464	9	0.7
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP013855	Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence	205942-205973	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP011869	Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence	155499-155530	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MT521993	Gordonia phage RedWattleHog, complete genome	65055-65086	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MN586040	Gordonia phage Stormageddon, complete genome	65036-65067	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	690146-690177	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP013072	Sphingobium indicum B90A plasmid pSRL2, complete sequence	10935-10966	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NC_023316	Streptomyces sp. 14R-10 plasmid pZL1, complete sequence	95519-95550	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP018081	Sulfitobacter sp. AM1-D1 plasmid unnamed5, complete sequence	147019-147050	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MH651167	Gordonia phage Angelique, complete genome	41404-41435	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MK937608	Microbacterium phage Cressida, complete genome	1608-1639	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	HM152765	Mycobacterium phage Island3, complete genome	682-713	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NC_011291	Mycobacterium phage Brujita, complete genome	682-713	9	0.719
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MN813682	Microbacterium phage Matzah, complete genome	1611-1642	9	0.719
NZ_CP017172_19	19.13\|8874363\|34\|NZ_CP017172\|CRISPRCasFinder,CRT	8874363-8874396	34	NZ_CP009112	Rhodococcus opacus strain 1CP plasmid pR1CP1, complete sequence	84026-84059	9	0.735
NZ_CP017172_19	19.13\|8874363\|34\|NZ_CP017172\|CRISPRCasFinder,CRT	8874363-8874396	34	NC_017507	Marinobacter adhaerens HP15 plasmid pHP-187, complete sequence	112472-112505	9	0.735
NZ_CP017172_19	19.15\|8874508\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874508-8874539	32	NZ_CP013105	Paraburkholderia caribensis strain MWAP64 plasmid 2, complete sequence	8779-8810	9	0.719
NZ_CP017172_19	19.16\|8874577\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874577-8874608	32	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	4898-4929	9	0.719
NZ_CP017172_19	19.16\|8874577\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8874577-8874608	32	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	57958-57989	9	0.719
NZ_CP017172_19	19.20\|8874861\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874861-8874893	33	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	723996-724028	9	0.727
NZ_CP017172_19	19.20\|8874861\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874861-8874893	33	GU911303	Burkholderia phage KS5, complete genome	29579-29611	9	0.727
NZ_CP017172_19	19.22\|8875002\|32\|NZ_CP017172\|CRISPRCasFinder,CRT	8875002-8875033	32	CP054921	Streptomyces sp. NA03103 plasmid unnamed1, complete sequence	14127-14158	9	0.719
NZ_CP017172_19	19.26\|8875286\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875286-8875319	34	MN224564	Streptomyces phage Araceli, complete genome	3308-3341	9	0.735
NZ_CP017172_19	19.26\|8875286\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875286-8875319	34	MH229863	Streptomyces phage JackieB, complete genome	3184-3217	9	0.735
NZ_CP017172_19	19.26\|8875286\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875286-8875319	34	MH229862	Streptomyces phage Henoccus, complete genome	3308-3341	9	0.735
NZ_CP017172_19	19.27\|8875357\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875357-8875390	34	NZ_CP048425	Rhizobium daejeonense strain KACC 13094 plasmid unnamed2, complete sequence	200992-201025	9	0.735
NZ_CP017172_19	19.29\|8875498\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875498-8875530	33	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	2264955-2264987	9	0.727
NZ_CP017172_19	19.29\|8875498\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875498-8875530	33	NZ_CP020812	Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed3, complete sequence	18686-18718	9	0.727
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP054028	Rhizobium sp. JKLM19E plasmid pPR19E01, complete sequence	588047-588078	9	0.719
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050104	Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence	1069173-1069204	9	0.719
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050109	Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence	1069176-1069207	9	0.719
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP030761	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence	788571-788602	9	0.719
NZ_CP017172_19	19.40\|8876275\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876275-8876306	32	NC_015188	Acidiphilium multivorum AIU301 plasmid pACMV4, complete sequence	22012-22043	9	0.719
NZ_CP017172_19	19.41\|8876344\|37\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876344-8876380	37	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	516033-516069	9	0.757
NZ_CP017172_19	19.41\|8876344\|37\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876344-8876380	37	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	57775-57811	9	0.757
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	NC_015314	Pseudonocardia dioxanivorans CB1190 plasmid pPSED01, complete sequence	180301-180333	9	0.727
NZ_CP017172_19	19.58\|8877551\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877551-8877584	34	NZ_CP041652	Streptomyces sp. RLB1-9 plasmid pRLB1-9.2, complete sequence	68632-68665	9	0.735
NZ_CP017172_19	19.58\|8877551\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877551-8877584	34	KY290947	Aeromonas phage 3, complete genome	10379-10412	9	0.735
NZ_CP017172_19	19.60\|8877693\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877693-8877725	33	NZ_CP022999	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence	999854-999886	9	0.727
NZ_CP017172_19	19.63\|8877906\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877906-8877939	34	NZ_CP035508	Haematobacter massiliensis strain OT1 plasmid pOT1-8, complete sequence	64252-64285	9	0.735
NZ_CP017172_19	19.65\|8878049\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878049-8878081	33	MT498055	Arthrobacter phage Bumble, complete genome	24917-24949	9	0.727
NZ_CP017172_19	19.67\|8878189\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878189-8878222	34	NC_020062	Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence	505066-505099	9	0.735
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	499220-499251	9	0.719
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1313849-1313880	9	0.719
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NZ_CP019938	Ketogulonicigenium robustum strain SPU_B003 plasmid unnamed1, complete sequence	168370-168401	9	0.719
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	MT521993	Gordonia phage RedWattleHog, complete genome	132076-132107	9	0.719
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	MN586040	Gordonia phage Stormageddon, complete genome	133023-133054	9	0.719
NZ_CP017172_19	19.69\|8878332\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878332-8878363	32	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	698144-698175	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP021028	Rhizobium sp. TAL182 plasmid pRetTAL182d, complete sequence	410192-410223	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP013503	Rhizobium esperanzae strain N561 plasmid pRspN561c, complete sequence	409007-409038	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP013509	Rhizobium sp. N1341 plasmid pRspN1341d, complete sequence	409007-409038	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP013520	Rhizobium sp. N113 plasmid pRspN113c, complete sequence	409007-409038	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP013493	Rhizobium sp. N6212 plasmid pRspN6212c, complete sequence	409007-409038	9	0.719
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP013516	Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence	409524-409555	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_KY494864	Pseudomonas aeruginosa strain FFUP_PS_37 plasmid pJB37, complete sequence	267278-267309	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP009975	Pseudomonas putida S12 plasmid pTTS12, complete sequence	276015-276046	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP039991	Pseudomonas aeruginosa strain T2101 plasmid pBT2101, complete sequence	410419-410450	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_MN433457	Pseudomonas aeruginosa strain PAB546 plasmid pNK546-KPC, complete sequence	22823-22854	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP045003	Pseudomonas aeruginosa strain PAG5 plasmid pPAG5, complete sequence	290284-290315	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP045917	Pseudomonas aeruginosa strain CF39S plasmid pCF39S, complete sequence	432497-432528	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	MF344568	Pseudomonas aeruginosa plasmid p727-IMP, complete sequence	396411-396442	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	MF344569	Pseudomonas aeruginosa plasmid p12939-PER, complete sequence	467111-467142	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	CP027478	Pseudomonas koreensis strain P19E3 plasmid p1, complete sequence	46813-46844	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP040126	Pseudomonas aeruginosa strain PA298 plasmid pBM908, complete sequence	264761-264792	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP015879	Pseudomonas citronellolis strain SJTE-3 plasmid pRBL16, complete sequence	274137-274168	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_CP016215	Pseudomonas aeruginosa strain PA121617 plasmid pBM413, complete sequence	338669-338700	9	0.719
NZ_CP017172_19	19.73\|8878610\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878610-8878641	32	NZ_KY883660	Pseudomonas putida strain SY153 plasmid pSY153-MDR, complete sequence	434408-434439	9	0.719
NZ_CP017172_19	19.76\|8878819\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878819-8878850	32	NC_019519	Agrobacterium phage 7-7-1, complete genome	17096-17127	9	0.719
NZ_CP017172_19	19.78\|8878959\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878959-8878990	32	NZ_CP027299	Streptomyces sp. SGAir0924 plasmid unnamed_5	97435-97466	9	0.719
NZ_CP017172_19	19.81\|8879169\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879169-8879203	35	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	769472-769506	9	0.743
NZ_CP017172_19	19.81\|8879169\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879169-8879203	35	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	279085-279119	9	0.743
NZ_CP017172_19	19.82\|8879241\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879241-8879274	34	NZ_CP039697	Novosphingobium sp. ABRDHK2 plasmid pABRDHK22, complete sequence	417433-417466	9	0.735
NZ_CP017172_19	19.86\|8879531\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879531-8879562	32	NZ_CP017753	Cupriavidus sp. USMAHM13 plasmid unnamed1, complete sequence	212625-212656	9	0.719
NZ_CP017172_19	19.92\|8879959\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879959-8879991	33	NZ_CP026518	Deinococcus sp. NW-56 plasmid unnamed2, complete sequence	68832-68864	9	0.727
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	NZ_CP032326	Azospirillum brasilense strain MTCC4035 plasmid p5, complete sequence	269991-270024	9	0.735
NZ_CP017172_19	19.112\|8881386\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881386-8881417	32	NZ_CP023000	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence	150717-150748	9	0.719
NZ_CP017172_19	19.119\|8881880\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881880-8881911	32	NZ_CP029359	Azospirillum sp. CFH 70021 plasmid unnamed4	122068-122099	9	0.719
NZ_CP017172_19	19.120\|8881949\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881949-8881981	33	NZ_CP042268	Pseudomonas aeruginosa strain HOU1 plasmid pHOU1-1, complete sequence	74423-74455	9	0.727
NZ_CP017172_20	20.4\|9408406\|30\|NZ_CP017172\|CRT	9408406-9408435	30	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	444239-444268	9	0.7
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022775	Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence	972915-972946	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	376296-376327	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP040937	Hymenobacter sp. DG01 plasmid unnamed, complete sequence	203665-203696	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	972012-972043	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	869325-869356	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP023017	Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence	941601-941632	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	868440-868471	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	874087-874118	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	874076-874107	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	372167-372198	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	869317-869348	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	869335-869366	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	869309-869340	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022764	Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence	972999-973030	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022797	Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence	972995-973026	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	NZ_CP022758	Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence	972980-973011	10	0.688
NZ_CP017172_11	11.1\|5618434\|32\|NZ_CP017172\|CRISPRCasFinder	5618434-5618465	32	MK937591	Microbacterium phage Cinna, complete genome	1611-1642	10	0.688
NZ_CP017172_19	19.13\|8874363\|34\|NZ_CP017172\|CRISPRCasFinder,CRT	8874363-8874396	34	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	754053-754086	10	0.706
NZ_CP017172_19	19.14\|8874434\|37\|NZ_CP017172\|CRISPRCasFinder,CRT	8874434-8874470	37	NZ_CP033968	Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed1, complete sequence	214698-214734	10	0.73
NZ_CP017172_19	19.14\|8874434\|37\|NZ_CP017172\|CRISPRCasFinder,CRT	8874434-8874470	37	NZ_CP037902	Cupriavidus metallidurans strain BS1 plasmid p1, complete sequence	90353-90389	10	0.73
NZ_CP017172_19	19.20\|8874861\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8874861-8874893	33	MT701591	Burkholderia phage Mana, complete genome	5061-5093	10	0.697
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050092	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence	718751-718782	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050081	Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence	638035-638066	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050098	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence	798574-798605	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050104	Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence	130732-130763	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP049731	Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence	672266-672297	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP053440	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence	869230-869261	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP018229	Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence	1120408-1120439	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP025507	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence	1111350-1111381	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP016287	Rhizobium leguminosarum strain Vaf10 plasmid unnamed1, complete sequence	692995-693026	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_HG938356	Neorhizobium galegae bv. officinalis bv. officinalis str. HAMBI 1141 plasmid pHAMBI1141a, complete sequence	1450858-1450889	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050109	Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence	130732-130763	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP030761	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence	476783-476814	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP054022	Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence	526706-526737	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NC_012848	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence	467776-467807	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP022666	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence	534887-534918	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP054032	Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence	240483-240514	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP022565	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK01, complete sequence	813556-813587	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP053206	Rhizobium leguminosarum bv. trifolii TA1 plasmid pRltTA1D, complete sequence	673457-673488	10	0.688
NZ_CP017172_19	19.31\|8875640\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875640-8875671	32	NZ_CP050086	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence	130802-130833	10	0.688
NZ_CP017172_19	19.42\|8876418\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876418-8876449	32	MT664984	Xanthomonas phage Xp12, complete genome	52683-52714	10	0.688
NZ_CP017172_19	19.43\|8876487\|36\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8876487-8876522	36	NC_008043	Ruegeria sp. TM1040 megaplasmid, complete sequence	115782-115817	10	0.722
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	KU160664	Arthrobacter phage Salgado, complete genome	5797-5829	10	0.697
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	MF140418	Arthrobacter phage LiSara, complete genome	5820-5852	10	0.697
NZ_CP017172_19	19.57\|8877481\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877481-8877513	33	KU160654	Arthrobacter phage Laroye, complete genome	5789-5821	10	0.697
NZ_CP017172_19	19.58\|8877551\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877551-8877584	34	NC_008757	Polaromonas naphthalenivorans CJ2 plasmid pPNAP01, complete sequence	56288-56321	10	0.706
NZ_CP017172_19	19.58\|8877551\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877551-8877584	34	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	340531-340564	10	0.706
NZ_CP017172_19	19.63\|8877906\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877906-8877939	34	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	722697-722730	10	0.706
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP015585	Roseomonas gilardii strain U14-5 plasmid 1, complete sequence	8-39	10	0.688
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP021032	Rhizobium sp. NXC14 plasmid pRspNXC14b, complete sequence	668178-668209	10	0.688
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP024587	Roseomonas sp. FDAARGOS_362 plasmid unnamed3, complete sequence	138654-138685	10	0.688
NZ_CP017172_19	19.71\|8878471\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8878471-8878502	32	NZ_CP006373	Aureimonas sp. AU20 plasmid pAU20f, complete sequence	10275-10306	10	0.688
NZ_CP017172_19	19.82\|8879241\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879241-8879274	34	NZ_CP017300	Rhodococcus sp. YL-1 plasmid pYLC1, complete sequence	233082-233115	10	0.706
NZ_CP017172_19	19.86\|8879531\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879531-8879562	32	MN693118	Marine virus AFVG_25M91, complete genome	55965-55996	10	0.688
NZ_CP017172_19	19.86\|8879531\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8879531-8879562	32	MN693323	Marine virus AFVG_25M87, complete genome	5401-5432	10	0.688
NZ_CP017172_19	19.96\|8880242\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880242-8880276	35	NZ_CP050094	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b4, complete sequence	303858-303892	10	0.714
NZ_CP017172_19	19.96\|8880242\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880242-8880276	35	NC_008379	Rhizobium leguminosarum bv. viciae 3841 plasmid pRL9, complete sequence	286979-287013	10	0.714
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	MN586025	Mycobacterium phage Mdavu, complete genome	19106-19139	10	0.706
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	KT281789	Mycobacterium phage Enkosi, complete genome	19118-19151	10	0.706
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	MH020245	Mycobacterium phage SgtBeansprout, complete genome	19118-19151	10	0.706
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	KX808132	Mycobacterium phage Amelie, complete genome	19118-19151	10	0.706
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	MH399770	Mycobacterium phage Biglebops, complete genome	19118-19151	10	0.706
NZ_CP017172_19	19.106\|8880956\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8880956-8880989	34	MF919518	Mycobacterium phage LilPharaoh, complete genome	19118-19151	10	0.706
NZ_CP017172_19	19.109\|8881171\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881171-8881204	34	NZ_CP014802	Salipiger profundus strain JLT2016 plasmid pTPRO6, complete sequence	100081-100114	10	0.706
NZ_CP017172_19	19.112\|8881386\|32\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8881386-8881417	32	NZ_CP018075	Streptomyces venezuelae strain NRRL B-65442 plasmid, complete sequence	74617-74648	10	0.688
NZ_CP017172_19	19.123\|8882160\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8882160-8882192	33	NZ_CP049358	Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence	86223-86255	10	0.697
NZ_CP017172_19	19.123\|8882160\|33\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8882160-8882192	33	NZ_CP031159	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence	74701-74733	10	0.697
NZ_CP017172_19	19.4\|8873727\|33\|NZ_CP017172\|CRISPRCasFinder,CRT	8873727-8873759	33	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	1612383-1612415	11	0.667
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MN234182	Mycobacterium phage Geraldini, complete genome	32753-32787	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MN234198	Mycobacterium phage Zavala, complete genome	31985-32019	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MK460247	Mycobacterium phage YoureAdopted, complete genome	31908-31942	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MH513977	Mycobacterium phage Mynx, complete genome	32025-32059	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MH371113	Mycobacterium phage Beezoo, complete genome	32668-32702	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	MF377440	Mycobacterium phage Bella96, complete genome	32562-32596	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	KX657796	Mycobacterium phage Urkel, complete genome	32606-32640	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	KX657794	Mycobacterium phage SamuelLPlaqson, complete genome	32606-32640	11	0.686
NZ_CP017172_19	19.34\|8875851\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875851-8875885	35	KX657795	Mycobacterium phage DrHayes, complete genome	32606-32640	11	0.686
NZ_CP017172_19	19.62\|8877835\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877835-8877868	34	NZ_CP022195	Yangia pacifica strain YSBP01 plasmid unnamed5, complete sequence	47149-47182	11	0.676
NZ_CP017172_19	19.62\|8877835\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877835-8877868	34	JN699011	Mycobacterium phage Stinger, complete genome	29579-29612	11	0.676
NZ_CP017172_19	19.62\|8877835\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877835-8877868	34	NC_011044	Mycobacterium phage Nigel, complete genome	29888-29921	11	0.676
NZ_CP017172_19	19.62\|8877835\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877835-8877868	34	KR080200	Mycobacterium phage AlanGrant, complete genome	31723-31756	11	0.676
NZ_CP017172_19	19.62\|8877835\|34\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8877835-8877868	34	KR080194	Mycobacterium phage Vincenzo, complete genome	31723-31756	11	0.676
NZ_CP017172_19	19.13\|8874363\|34\|NZ_CP017172\|CRISPRCasFinder,CRT	8874363-8874396	34	NZ_CP024895	Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence	159586-159619	12	0.647

1. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_003085 (Myxococcus phage Mx8, complete genome) position: , mismatch: 2, identity: 0.938

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
caccgcgcccgcatcgccccgacgcccacgcc	Protospacer
  ******************************

2. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to AF396866 (Bacteriophage Mx8, complete genome) position: , mismatch: 2, identity: 0.938

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
caccgcgcccgcatcgccccgacgcccacgcc	Protospacer
  ******************************

3. spacer 14.1|7201994|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP017242 (Rhizobium etli 8C-3 plasmid pRsp8C3a, complete sequence) position: , mismatch: 3, identity: 0.88

tggggctcgccctctccgtcgtcct	CRISPR spacer
cggggctcggcctttccgtcgtcct	Protospacer
.******** ***.***********

4. spacer 14.1|7201994|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP035001 (Rhizobium acidisoli strain FH23 plasmid pRapFH23c, complete sequence) position: , mismatch: 3, identity: 0.88

tggggctcgccctctccgtcgtcct	CRISPR spacer
cgggcttcgccctctccgtcgtcct	Protospacer
.*** .*******************

5. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP054620 (Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence) position: , mismatch: 3, identity: 0.88

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccatgccgccatcgaggt	Protospacer
*********************  *

6. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP032685 (Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence) position: , mismatch: 3, identity: 0.88

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccttgccgccatcgccgt	Protospacer
********* ************.*

7. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP032690 (Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence) position: , mismatch: 3, identity: 0.88

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccttgccgccatcgccgt	Protospacer
********* ************.*

8. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP028919 (Gemmobacter sp. HYN0069 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.88

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccaagccgccatcgccga	Protospacer
********** ***********.*.

9. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021355 (Rhodococcus sp. S2-17 plasmid pRB98, complete sequence) position: , mismatch: 4, identity: 0.875

gcgcgcccggcgcacccggcggcgg-catgcct	CRISPR spacer
gggcgcccggcggacccggcggcggccatggc-	Protospacer
* ********** ************ **** *

10. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to CP003957 (Rhodococcus opacus PD630 plasmid 8, complete sequence) position: , mismatch: 4, identity: 0.875

gcgcgcccggcgcacccggcggcgg-catgcct	CRISPR spacer
gggcgcccggcggacccggcggcggccatggc-	Protospacer
* ********** ************ **** *

11. spacer 14.1|7201994|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP011665 (Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence) position: , mismatch: 4, identity: 0.84

tggggctcgccctctccgtcgtcct	CRISPR spacer
ccgggctcgccctcgccgtcgacct	Protospacer
. ************ ****** ***

12. spacer 14.1|7201994|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 4, identity: 0.84

tggggctcgccctctccgtcgtcct	CRISPR spacer
tggggctcgccctcgccgtcgatcc	Protospacer
************** ****** .*.

13. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_AP021845 (Azospira sp. I09 plasmid pAZI09, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
atcccgtccatcccgccatcgctgg	Protospacer
 . ******** *************

14. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
atgccgaccatgccgccgtcgctgg	Protospacer
 .**** **********.*******

15. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP020399 (Burkholderia multivorans strain FDAARGOS_246 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
gcgccgtacatgccgccattgctgc	Protospacer
 ****** ***********.****

16. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccatgccgccgtcgaggt	Protospacer
*****************.***  *

17. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP041653 (Streptomyces sp. RLB1-9 plasmid pRLB1-9.1, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgaccatgccgccatcgacgc	Protospacer
****** ************** .*

18. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
gcgccgtctatgacgccatcgctgc	Protospacer
 *******.*** ***********

19. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_AP012556 (Mycobacterium avium subsp. hominissuis TH135 plasmid pMAH135, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
tcgccgttcttgccgccatcgctgt	Protospacer
.******.* **************

20. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP007792 (Corynebacterium marinum DSM 44953 plasmid pCmarinum1, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
tcgccgtccatgccgcctccgctgt	Protospacer
.**************** .*****

21. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NC_014755 (Sulfuricurvum kujiense DSM 16994 plasmid pSULKU02, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
gcgccgtcgatgccgccatcgatgc	Protospacer
 ******* ************ **

22. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 4, identity: 0.84

ccgccgtccatgccgccatcgctgg	CRISPR spacer
ccgccgtccatgccgtcatcgaggt	Protospacer
***************.*****  *

23. spacer 5.1|1398094|25|NZ_CP017172|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
  ** ******************

24. spacer 14.4|7202141|25|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021830 (Sinorhizobium meliloti strain HM006 plasmid psymA, complete sequence) position: , mismatch: 5, identity: 0.8

ccgccgtccatgccgccatcgctgg	CRISPR spacer
tcgccgcccatgccgccatcgccat	Protospacer
.*****.***************..

25. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

26. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

27. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

28. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

29. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

30. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

31. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

32. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

33. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

34. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

35. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

36. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

37. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

38. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

39. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

40. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

41. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

42. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

43. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

44. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

45. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

46. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

47. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

48. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

49. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

50. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

51. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

52. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

53. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

54. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

55. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

56. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

57. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

58. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

59. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

60. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

61. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

62. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

63. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

64. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

65. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

66. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

67. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

68. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

69. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

70. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

71. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

72. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

73. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

74. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

75. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.821

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggc	Protospacer
*****.******** ******** * .*

76. spacer 19.15|8874508|32|NZ_CP017172|CRISPRCasFinder,CRT matches to MH651167 (Gordonia phage Angelique, complete genome) position: , mismatch: 5, identity: 0.844

accaccggcccgaggagcggctcgcacgagag	CRISPR spacer
tcgagcggcccgagaagcggctcgcatgagag	Protospacer
 * * *********.***********.*****

77. spacer 19.15|8874508|32|NZ_CP017172|CRISPRCasFinder,CRT matches to MT952844 (Gordonia phage Bosnia, complete genome) position: , mismatch: 5, identity: 0.844

accaccggcccgaggagcggctcgcacgagag	CRISPR spacer
tcgagcggcccgagaagcggttcgcacgagag	Protospacer
 * * *********.*****.***********

78. spacer 19.112|8881386|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020568 (Kitasatospora aureofaciens strain DM-1 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.844

agggcgggcgggcagtcgcggacgtggg-tgct	CRISPR spacer
ccggcggggggccagtcgcggacgtgggatgc-	Protospacer
  ****** ** **************** ***

79. spacer 20.1|9408237|29|NZ_CP017172|CRT matches to NZ_CP040720 (Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.828

gtgcagatgcgctgcggtgaacgctgcca	CRISPR spacer
tggcggatgcgctgcggagaacgctgcga	Protospacer
  **.************ ********* *

80. spacer 20.1|9408237|29|NZ_CP017172|CRT matches to NZ_CP018759 (Pseudomonas psychrotolerans strain PRS08-11306 plasmid pPRS08-11306, complete sequence) position: , mismatch: 5, identity: 0.828

gtgcagatgcgctgcggtgaacgc-tgcca	CRISPR spacer
ttgcagatgcgccgcggtgatcgcatgtc-	Protospacer
 ***********.******* *** **.*

81. spacer 7.1|3414411|30|NZ_CP017172|CRT matches to MN119376 (Streptomyces phage Geostin, complete genome) position: , mismatch: 6, identity: 0.8

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

82. spacer 7.1|3414411|30|NZ_CP017172|CRT matches to MH155868 (Streptomyces phage FlowerPower, complete genome) position: , mismatch: 6, identity: 0.8

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

83. spacer 7.1|3414411|30|NZ_CP017172|CRT matches to MN284894 (Streptomyces phage Fabian, complete genome) position: , mismatch: 6, identity: 0.8

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

84. spacer 7.3|3414516|30|NZ_CP017172|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 6, identity: 0.8

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

85. spacer 7.3|3414516|30|NZ_CP017172|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
 ***. .****** ********** *****

86. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_AP014706 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence) position: , mismatch: 6, identity: 0.812

gcgcgcccggcgcacccggcggc--ggcatgcct	CRISPR spacer
gcgcgcccggcgcacgcggcggcttggcgagg--	Protospacer
*************** *******  ***. *

87. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 6, identity: 0.786

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggt	Protospacer
*****.******** ******** * ..

88. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 6, identity: 0.786

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
tcgccagcatccggccgcccaccctggt	Protospacer
*****.******** ******** * ..

89. spacer 19.13|8874363|34|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.824

-actacgcggtggtgcgcggacgcgacgcgcacgg	CRISPR spacer
ggcgacg-gttgctgcgcggacgcgacgtgcacgg	Protospacer
 .* *** * ** ***************.******

90. spacer 19.15|8874508|32|NZ_CP017172|CRISPRCasFinder,CRT matches to MT521999 (Gordonia Phage Jablanski, complete genome) position: , mismatch: 6, identity: 0.812

accaccggcccgaggagcggctcgcacgagag	CRISPR spacer
tcgagtggcccgaggagcggttcgcaggagag	Protospacer
 * * .**************.***** *****

91. spacer 19.42|8876418|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033971 (Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.812

cccagcagctccagcttgccccgccactgctc-	CRISPR spacer
gccagcggctccagcttgcgccg-cagggctcg	Protospacer
 *****.************ *** **  ****

92. spacer 19.120|8881949|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.818

cgcggca-agctggaactgctgggctaccgcatg	CRISPR spacer
-ggggcgcagctggaatcgctgggctaccgcatc	Protospacer
 * ***. ********..***************

93. spacer 19.120|8881949|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.818

cgcggca-agctggaactgctgggctaccgcatg	CRISPR spacer
-ggggcgcagctggaatcgctgggctaccgcatc	Protospacer
 * ***. ********..***************

94. spacer 19.120|8881949|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 6, identity: 0.818

cgcggca-agctggaactgctgggctaccgcatg	CRISPR spacer
-ggggcgcagctggaatcgctgggctaccgcatc	Protospacer
 * ***. ********..***************

95. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_AP014706 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence) position: , mismatch: 7, identity: 0.781

gcgcgcccggcgcacccggcggc--ggcatgcct	CRISPR spacer
gcacgcccggcgcacgcggcggcttggcgagg--	Protospacer
**.************ *******  ***. *

96. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_AP014706 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_2p, complete sequence) position: , mismatch: 7, identity: 0.781

gcgcgcccggcgcacccggcggc--ggcatgcct	CRISPR spacer
gcacgcccggcgcacgcggcggcttggcgagg--	Protospacer
**.************ *******  ***. *

97. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 7, identity: 0.781

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gagcgcccggcgcacctggcggcgggccgcgg	Protospacer
* **************.********  .**

98. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP015090 (Pelagibaca abyssi strain JLT2014 plasmid pPABY2, complete sequence) position: , mismatch: 7, identity: 0.781

gcgcgcccggcgcacccggcggcggcatgcct---	CRISPR spacer
gcgcccccggcgcac---gcggcggcacggcgggg	Protospacer
**** **********   *********.* *

99. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP007453 (Peptoclostridium acidaminophilum DSM 3953 strain al-2 plasmid EAL2_808p, complete sequence) position: , mismatch: 7, identity: 0.781

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gtgccggctgcgaactcggcggcggcatgcct	Protospacer
*.**   * *** **.****************

100. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to AM261282 (Uncultured bacterium IncP-1 plasmid pKJK5 complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

101. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_CP028340 (Thauera aromatica K172 plasmid pKJK172, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

102. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to KC964605 (Uncultured bacterium plasmid pMLUA1, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

103. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to KC964606 (Uncultured bacterium plasmid pMLUA3, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

104. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to KC964607 (Uncultured bacterium plasmid pMLUA4, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

105. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_MN366356 (Bacterium plasmid pALTS27, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

106. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to NZ_MN366360 (Bacterium plasmid pALTS32, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

107. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to JQ004406 (Uncultured bacterium plasmid pHH128, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

108. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to JQ004407 (Uncultured bacterium plasmid pHH3408, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

109. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to JQ004408 (Uncultured bacterium plasmid pHH3414, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

110. spacer 14.6|7202261|28|NZ_CP017172|CRISPRCasFinder matches to JQ004409 (Uncultured bacterium plasmid pKS77, complete sequence) position: , mismatch: 7, identity: 0.75

tcgccggcatccgggcgcccaccatcac	CRISPR spacer
ccgccggcatccgggcgggcaccaaggg	Protospacer
.****************  *****  .

111. spacer 19.11|8874225|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 7, identity: 0.788

ggcgcggccttcccggcgctgcctgcgcttggg	CRISPR spacer
ggcgcggccttcccgccgcagcctgctcaagac	Protospacer
*************** *** ****** *  *.

112. spacer 19.15|8874508|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP006370 (Aureimonas sp. AU20 plasmid pAU20c, complete sequence) position: , mismatch: 7, identity: 0.781

accaccggcccgaggagcggctcgcacgagag	CRISPR spacer
accaccggcccgatcagcggctcgggcgcgtt	Protospacer
*************  ********* .** *

113. spacer 19.16|8874577|32|NZ_CP017172|CRISPRCasFinder,CRT matches to MK494099 (Mycobacterium phage Typha, complete genome) position: , mismatch: 7, identity: 0.781

cgaggcgcccacgctccccactgtttgaagaa	CRISPR spacer
gctggtgcccacgctccccactgcttgaacag	Protospacer
   **.*****************.***** *.

114. spacer 19.16|8874577|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP018385 (Burkholderia pseudomallei strain 2008724860 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.781

cgaggcgcccacgctccccactgtttgaagaa	CRISPR spacer
caggggagccactcgccccactgtttgaagaa	Protospacer
*..** . **** * *****************

115. spacer 19.22|8875002|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP010408 (Streptomyces vietnamensis strain GIMV4.0001 plasmid pSVL1, complete sequence) position: , mismatch: 7, identity: 0.781

atctccaggatgcagcaggcctacctcaacgc	CRISPR spacer
accggcaccatgcaggaggcctacctcaaggc	Protospacer
*.*  **  ****** ************* **

116. spacer 19.37|8876066|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 7, identity: 0.781

cgccggggctccgggccatgatcatgggggag	CRISPR spacer
cgccggggatcagggccatgatcaggaagacg	Protospacer
******** ** ************ *..*. *

117. spacer 19.49|8876912|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to JQ768459 (Pseudomonas phage Lu11, complete genome) position: , mismatch: 7, identity: 0.781

ttgatgcgcaggtgggcgctcaccgcgtcgta	CRISPR spacer
ttgattcgcaggtggccgctcacccggacgcc	Protospacer
***** ********* ********  * **.

118. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039892 (Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499c, complete sequence) position: , mismatch: 7, identity: 0.788

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
aagttcgccggacgcggcccggtccgtcatggc	Protospacer
.*  ** *** ******************* *

119. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH178382 (Streptomyces phage Salete, complete genome) position: , mismatch: 7, identity: 0.788

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
gacgaccccgtacgcggccaggtccggcgcgtg	Protospacer
**** ************** ****** *..  *

120. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH178381 (Streptomyces phage BayC, complete genome) position: , mismatch: 7, identity: 0.788

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
gacgaccccgtacgcggccaggtccggcgcgtg	Protospacer
**** ************** ****** *..  *

121. spacer 19.70|8878401|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039433 (Rhodococcus sp. SGAir0479 plasmid unnamed) position: , mismatch: 7, identity: 0.788

gacgtcgtccacctgctggcccatgcggcgctt-	CRISPR spacer
cacgtcgtccacgtgctggccaatg-gatacttc	Protospacer
 *********** ******** *** *...***

122. spacer 19.78|8878959|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.781

-cgcgagcacaacctggtgggctccttcgtcgc	CRISPR spacer
gcgctgg-acgacctggtgggcttcttcgtcaa	Protospacer
 *** .* **.************.*******.

123. spacer 19.81|8879169|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to ASAB01000001 (Pectobacterium atrosepticum CFBP 6276 plasmid pL1Pa6276, complete sequence, whole genome shotgun sequence) position: , mismatch: 7, identity: 0.8

-cgccgcatctggaggggctgccggtgaaggcgtgg	CRISPR spacer
acggc-tatctggtggtgctgccggtgaaggcgtac	Protospacer
 ** * .****** ** *****************.

124. spacer 19.92|8879959|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR594663 (Variovorax sp. RA8 plasmid 2) position: , mismatch: 7, identity: 0.788

acaaggcgcccacgtgccctgcctgc-cgctcta	CRISPR spacer
cgaaggcgcccacgtaccatgcctgcgcgcgcc-	Protospacer
  *************.** ******* *** *.

125. spacer 20.3|9408350|30|NZ_CP017172|CRT matches to NZ_CP039919 (Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626b, complete sequence) position: , mismatch: 7, identity: 0.767

ctgctgctgcggtcgggctcaccgtctcaa	CRISPR spacer
tttcgtcttcggtcgggttcaccgtctcat	Protospacer
.* *  ** ********.***********

126. spacer 20.3|9408350|30|NZ_CP017172|CRT matches to NC_008269 (Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence) position: , mismatch: 7, identity: 0.767

ctgctgctgcggtcgggctcaccgtctcaa	CRISPR spacer
gcggcgccgcggtcgggctcaccgtgtcca	Protospacer
 .* .**.***************** ** *

127. spacer 3.1|1043968|31|NZ_CP017172|CRISPRCasFinder matches to NZ_CP025513 (Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.742

gcgccgtgtccgctcgtcgccaaggcttccg	CRISPR spacer
ccgccgtatccgctcttcgccaagacggcga	Protospacer
 ******.******* ********.*  * .

128. spacer 3.1|1043968|31|NZ_CP017172|CRISPRCasFinder matches to MN310546 (Microbacterium phage PhriedRice, complete genome) position: , mismatch: 8, identity: 0.742

gcgccgtgtccgctcgtcgccaaggcttccg	CRISPR spacer
gagatcgctccgctcatcgcgaaggcttccg	Protospacer
* * .   *******.**** **********

129. spacer 3.1|1043968|31|NZ_CP017172|CRISPRCasFinder matches to MT310890 (Microbacterium phage Phedro, complete genome) position: , mismatch: 8, identity: 0.742

gcgccgtgtccgctcgtcgccaaggcttccg	CRISPR spacer
gagatcgctccgctcatcgcgaaggcttccg	Protospacer
* * .   *******.**** **********

130. spacer 3.1|1043968|31|NZ_CP017172|CRISPRCasFinder matches to MT310889 (Microbacterium phage Phractured, complete genome) position: , mismatch: 8, identity: 0.742

gcgccgtgtccgctcgtcgccaaggcttccg	CRISPR spacer
gagatcgctccgctcatcgcgaaggcttccg	Protospacer
* * .   *******.**** **********

131. spacer 3.1|1043968|31|NZ_CP017172|CRISPRCasFinder matches to MT310891 (Microbacterium phage Pharky, complete genome) position: , mismatch: 8, identity: 0.742

gcgccgtgtccgctcgtcgccaaggcttccg	CRISPR spacer
gagatcgctccgctcatcgcgaaggcttccg	Protospacer
* * .   *******.**** **********

132. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to KJ538722 (Mycobacterium phage HH92, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

133. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to KT222940 (Mycobacterium phage Kinbote, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

134. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MH727549 (Mycobacterium phage Gancho, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

135. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MK919482 (Mycobacterium phage DeepSoil15, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

136. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MT657330 (Mycobacterium phage Webster2, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

137. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MF919517 (Mycobacterium phage LilHazelnut, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

138. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to EU203571 (Mycobacterium phage Giles, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

139. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MK494095 (Mycobacterium phage Daegal, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

140. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MT818421 (Mycobacterium phage Luke, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

141. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MH697577 (Mycobacterium phage Amochick, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

142. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MT684594 (Mycobacterium phage Hadrien, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

143. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MT114159 (Mycobacterium phage Ein37, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

144. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to KT246485 (Mycobacterium phage OBUpride, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

145. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to KT454972 (Mycobacterium phage Evanesce, complete genome) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgggcggcgcacccggcggcggcggtaac	Protospacer
*****  *******************.    .

146. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021915 (Sagittula sp. P11 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcgtcggtggcgaacccggcggcggcatccct	Protospacer
 **.   .**** *************** ***

147. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_LR594692 (Variovorax sp. WDL1 plasmid 4) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
catcggccggcgcacccgccggcggcacaccg	Protospacer
   ** ************ ********..**

148. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NC_011368 (Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG201, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcgcgcccggcgcatccggctgcggttcggcg	Protospacer
 *************.***** ****. .* *

149. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP031599 (Roseovarius indicus strain DSM 26383 plasmid pRIdsm_01, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcgtcggcggcgaacccggcggcggcattccc	Protospacer
 **.   ***** *************** **.

150. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP045373 (Sulfitobacter sp. THAF37 plasmid pTHAF37_a, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcgtcggcggcgaacccggcggcggcattccc	Protospacer
 **.   ***** *************** **.

151. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
ccgcgcccggcgcaccccgaggcggaaacgcg	Protospacer
 **************** * ***** *   *

152. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP049732 (Rhizobium leguminosarum strain A1 plasmid pRL11, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgccctgcgcagccggcggctccagtatt	Protospacer
******** ***** ********  **   .*

153. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct-	CRISPR spacer
acgggcccggcgcacccggccgc-gtacaccac	Protospacer
.** **************** ** *.*..**

154. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct------	CRISPR spacer
gcgcgcccggcggaccgggcggc------cctcccggc	Protospacer
************ *** ******      ***

155. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021805 (Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence) position: , mismatch: 8, identity: 0.75

-gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
ttcgtg-acggcgcactcggcggcggcaagctc	Protospacer
  **.*  ********.*********** **..

156. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP021807 (Sinorhizobium meliloti strain T073 plasmid accessoryA, complete sequence) position: , mismatch: 8, identity: 0.75

-gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
ttcgtg-acggcgcactcggcggcggcaagctc	Protospacer
  **.*  ********.*********** **..

157. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP045549 (Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
acccggccggcccacccggcggcggcctcgcg	Protospacer
.* ** ***** ************** *  *

158. spacer 19.11|8874225|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NC_015382 (Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgcggccttcccggcgctgcctgcgcttggg	CRISPR spacer
gaggcggccttcctggcgctgcccgcgcggctg	Protospacer
*. **********.*********.****    *

159. spacer 19.11|8874225|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP048642 (Streptomyces aureoverticillatus strain HN6 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgcggccttcccggcgctgcctgcgcttggg	CRISPR spacer
gcgccaactttcccggccctgcctccgcttggg	Protospacer
*   *..*.******** ****** ********

160. spacer 19.11|8874225|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP022418 (Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-3, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgcggccttcccggcgctgcctgcgcttggg---	CRISPR spacer
cgcgcggcattcccggcgctgcgtg---tcgagacc	Protospacer
 ******* ************* **   *.*.*

161. spacer 19.16|8874577|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP046254 (Sphingobium sp. CAP-1 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

cgaggcgcccacgctccccactgtttgaagaa	CRISPR spacer
agcagcgcccacgcaccccactgttcgaattc	Protospacer
 * .********** **********.***

162. spacer 19.20|8874861|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP021805 (Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence) position: , mismatch: 8, identity: 0.758

tgggccggcgtcctggagggtgccgcctggagg	CRISPR spacer
ggggccggcggcctggacggtgccgccaacggt	Protospacer
 ********* ****** ********* . .*

163. spacer 19.27|8875357|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.765

agcgcgagaatcgggcggcaccgtcgagttgccg	CRISPR spacer
cacgcgcgaatcgggcgtcaccgtcgacgggcag	Protospacer
 .**** ********** *********   ** *

164. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033968 (Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
tcgtcgctgtccagcatcacgaggttgcaaga	Protospacer
******..**************** . *   *

165. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP037902 (Cupriavidus metallidurans strain BS1 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
tcgtcgctgtccagcatcacgaggttgcaaga	Protospacer
******..**************** . *   *

166. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 8, identity: 0.75

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
tcgtcgtcggcccgcatcacgagcagcccgtg	Protospacer
********* ** ********** . **. *.

167. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.75

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
ccgtcgtcgtccagcgtcaccaggacggtgtc	Protospacer
.**************.**** ***.*  * *

168. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 8, identity: 0.75

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
tcgtcgtcggcccgcatcacgagcagcccgtg	Protospacer
********* ** ********** . **. *.

169. spacer 19.40|8876275|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030830 (Neorhizobium sp. NCHU2750 plasmid pNCHU2750c, complete sequence) position: , mismatch: 8, identity: 0.75

atcgtaggcggcgcccccatcgcccccgagaa	CRISPR spacer
atcgacggcggcgcccccatcgccattgactg	Protospacer
****  ****************** ..**  .

170. spacer 19.40|8876275|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_023286 (Streptomyces sp. F12 plasmid pFRL6, complete sequence) position: , mismatch: 8, identity: 0.75

atcgtaggcggcgcccccatcgcccccgagaa	CRISPR spacer
atactccgcggcccccccgtcgcccccgaggt	Protospacer
**  *  ***** *****.***********.

171. spacer 19.40|8876275|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN234195 (Mycobacterium phage Xula, complete genome) position: , mismatch: 8, identity: 0.75

atcgtaggcggcgcccccatcgcccccgagaa	CRISPR spacer
ctcgtaggcggcgcccagatcgccggggatga	Protospacer
 ***************  ******   ** .*

172. spacer 19.41|8876344|37|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.784

gccgcgacctcgcgcgctacatgggc-ctggacttcgt	CRISPR spacer
gccgcgacctcgcgcgcggcatgggcggcgagctgcg-	Protospacer
***************** .*******  .*..** **

173. spacer 19.42|8876418|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 8, identity: 0.75

cccagcagctccagcttgccccgccactgctc	CRISPR spacer
accagcaggtccagcttgccctgcggcgcatc	Protospacer
 ******* ************.** .*   **

174. spacer 19.47|8876771|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

caggtgtcgagctgtatcagcgcggaaatggg	CRISPR spacer
cgcttttcgagctggatcagcgcggacattgc	Protospacer
*.  * ******** *********** ** *

175. spacer 19.49|8876912|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.75

ttgatgcgcaggtgggcgctcaccgcgtcgta	CRISPR spacer
aggttgcgcaggtgggcgttcacctcgtccgg	Protospacer
  * **************.***** ****  .

176. spacer 19.54|8877268|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 8, identity: 0.758

gttctggccgcccaccttcgtacgctcggccag	CRISPR spacer
gtccatgccgcccgccttcatacgctcggctgc	Protospacer
**.*  *******.*****.**********..

177. spacer 19.55|8877338|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 8, identity: 0.765

tttccaagctgcagcgacgtctgccgcgctcagg	CRISPR spacer
gcttacggctgcagcgacgtcggccgcgcacagg	Protospacer
 .*.  .************** ******* ****

178. spacer 19.55|8877338|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 8, identity: 0.765

tttccaagctgcagcgacgtctgccgcgctcagg	CRISPR spacer
gcttacggctgcagcgacgtcggccgcgcacagg	Protospacer
 .*.  .************** ******* ****

179. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020897 (Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgaggtgccggcggaggcgctgatgggccggga	Protospacer
 *  ..*.****************** * ****

180. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_012854 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132505, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgcggtgccggccgaggcgctgatgggcaggga	Protospacer
 *. ..*.**** ************* ******

181. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_007764 (Rhizobium etli CFN 42 plasmid p42c, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgaggtgccggccgaggcgctgatgggcaggga	Protospacer
 *  ..*.**** ************* ******

182. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_021907 (Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1b, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgaggtgccggccgaggcgctgatgggcaggga	Protospacer
 *  ..*.**** ************* ******

183. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgccacgccggaggaggcgctgatggccgccgg	Protospacer
 *.****.*** ****************.  *.

184. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_013858 (Azospirillum sp. B510 plasmid pAB510d, complete sequence) position: , mismatch: 8, identity: 0.758

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgcccgctcggcggaggcgctgacggccacggt	Protospacer
 *.*   ****************.***** **

185. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KU530220 (Streptomyces phage Xkcd426, complete genome) position: , mismatch: 8, identity: 0.758

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
gtcgaccccgtacgcggccaggtccggcgcgtg	Protospacer
* ** ************** ****** *..  *

186. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.758

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
gagctgcccgtccgcggcccgggccgtcatgta	Protospacer
**  * ***** ********** *******  .

187. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 8, identity: 0.75

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
acctgcgcccgcatcgccccaacactgaagaa	Protospacer
***.****************.**.*. * *

188. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
acctgcgcccgcatcgccccaacactgaagaa	Protospacer
***.****************.**.*. * *

189. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 8, identity: 0.75

acccgcgcccgcatcgccccgacgcccacgcc--	CRISPR spacer
acccgcgcccgcatcg--ccgccacctggggcga	Protospacer
****************  *** *.**.. * *

190. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP053022 (Sphingobium yanoikuyae strain YC-XJ2 plasmid p-A-Sy, complete sequence) position: , mismatch: 8, identity: 0.75

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
gcggtcgatcgcaccgcccagacgcccacgcc	Protospacer
.*   ** .****.***** ************

191. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015090 (Pelagibaca abyssi strain JLT2014 plasmid pPABY2, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
cctgccggcgggcgccgccccggcgggtctgg	Protospacer
.************** **.*******.  . *

192. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_012807 (Methylorubrum extorquens AM1 plasmid p1META1, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
gctgccggcgggcgccggtccggcggggacgc	Protospacer
 ************** * ********...*

193. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg--	CRISPR spacer
ttcgccttcgggcgcagctccggcgg--gtcggt	Protospacer
*..***  ******************  *..*

194. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025014 (Rhizobium leguminosarum strain Norway plasmid pRLN2, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
tctgccggagggcgcagcgccggagcccaatg	Protospacer
******** ********* **** *   . **

195. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ggcgccggccggcgccgctccggcggtggccg	Protospacer
  .****** ***** ********** .**.*

196. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048282 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
tctgccggagggcgcagcgccggagccgaatg	Protospacer
******** ********* **** *  .. **

197. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022566 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK02, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
tctgccggagggcgcagcgccggagccgaatg	Protospacer
******** ********* **** *  .. **

198. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 8, identity: 0.75

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
gtggccggcgggcgcagcttcgacggcggcgg	Protospacer
 . ****************.**.*** .** *

199. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039909 (Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence) position: , mismatch: 8, identity: 0.75

---cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
atttgc---gcccgcgctatccgcgaatggcttga	Protospacer
   .**   *************** * *****..*

200. spacer 19.119|8881880|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_015727 (Cupriavidus necator N-1 plasmid pBB1, complete sequence) position: , mismatch: 8, identity: 0.75

gccact--cggtggagccctcggtggttgcccat	CRISPR spacer
--cgatgacggtgtagccctcggtggttgcctcg	Protospacer
  *. *  ***** *****************.

201. spacer 19.119|8881880|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020810 (Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

gccactcggtggagccctcggtggttgcccat	CRISPR spacer
accactcggtggagccgtcgatggccagccag	Protospacer
.*************** ***.***... ***

202. spacer 19.120|8881949|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022365 (Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence) position: , mismatch: 8, identity: 0.758

-cgcggcaagctggaactgctgggctaccgcatg	CRISPR spacer
atgtgg-aagccggaactgctgggcgaccgccgc	Protospacer
 .*.** ****.************* *****

203. spacer 19.123|8882160|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 8, identity: 0.758

tggacgcgcccgccgtgagcagcaccaggtcct	CRISPR spacer
tcagatcggccgccgtgagcggcaccaggtcca	Protospacer
* ..  ** ***********.***********

204. spacer 7.3|3414516|30|NZ_CP017172|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 9, identity: 0.7

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

205. spacer 7.3|3414516|30|NZ_CP017172|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
 ..********.**.*********** . .

206. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP013855 (Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
aggcgcccggcgaacccggcgtcggcgtagac	Protospacer
. ********** ******** ****.*.  .

207. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP011869 (Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
aggcgcccggcgaacccggcgtcggcgtagac	Protospacer
. ********** ******** ****.*.  .

208. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MT521993 (Gordonia phage RedWattleHog, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tgctgggcggcgctctcggcggcggcatgccg	Protospacer
   .*  ****** *.***************

209. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MN586040 (Gordonia phage Stormageddon, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tgctgggcggcgctctcggcggcggcatgccg	Protospacer
   .*  ****** *.***************

210. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct---	CRISPR spacer
ccgcgcccggcacatccggcggcg---cgtccagt	Protospacer
 **********.**.*********   .*.*.

211. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP013072 (Sphingobium indicum B90A plasmid pSRL2, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
ccgcgacgggcgcacccggcggcgaccgcgcg	Protospacer
 **** * ****************.*    *

212. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NC_023316 (Streptomyces sp. 14R-10 plasmid pZL1, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
cttcagctcgcgcacccggcggcggcccgcct	Protospacer
 . *. *. ***************** .****

213. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP018081 (Sulfitobacter sp. AM1-D1 plasmid unnamed5, complete sequence) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcgtcggtggcgaacccggcggcggcattccc	Protospacer
 **.   .**** *************** **.

214. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MH651167 (Gordonia phage Angelique, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
tcctgcccgccgcacccggcggccgcagcgca	Protospacer
 * .***** ************* ***   *

215. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MK937608 (Microbacterium phage Cressida, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
acctgctcggcgcacccggcgtcggcaagagc	Protospacer
.* .**.************** ***** *  .

216. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to HM152765 (Mycobacterium phage Island3, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gaacgcccggcgcaccctgcggctgccgtcag	Protospacer
* .************** ***** **   *

217. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NC_011291 (Mycobacterium phage Brujita, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gaacgcccggcgcaccctgcggctgccgtcag	Protospacer
* .************** ***** **   *

218. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MN813682 (Microbacterium phage Matzah, complete genome) position: , mismatch: 9, identity: 0.719

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
acctgctcggcgcacccggcgtcggcaagagc	Protospacer
.* .**.************** ***** *  .

219. spacer 19.13|8874363|34|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP009112 (Rhodococcus opacus strain 1CP plasmid pR1CP1, complete sequence) position: , mismatch: 9, identity: 0.735

actacgcggtggtgcgcggacgcgacgcgcacgg	CRISPR spacer
tgcgcgcggtggtgcgcggactcgatgccgccgg	Protospacer
  ..***************** ***.**   ***

220. spacer 19.13|8874363|34|NZ_CP017172|CRISPRCasFinder,CRT matches to NC_017507 (Marinobacter adhaerens HP15 plasmid pHP-187, complete sequence) position: , mismatch: 9, identity: 0.735

actacgcggtggtgcgcggacgcgacgcgcacgg	CRISPR spacer
tcctgccgaaggtgagcggacgcgacgcgcccgg	Protospacer
 *.   **. **** *************** ***

221. spacer 19.15|8874508|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP013105 (Paraburkholderia caribensis strain MWAP64 plasmid 2, complete sequence) position: , mismatch: 9, identity: 0.719

accaccggcccgaggagcggctcgcacgagag	CRISPR spacer
accaccggcccgtgtagcggctcaaatcaacc	Protospacer
************ * ********. *. *.

222. spacer 19.16|8874577|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 9, identity: 0.719

cgaggcgcccacgctccccactgtttgaagaa	CRISPR spacer
tcggcgatccactcgccccactgtttgaagaa	Protospacer
. .*  ..**** * *****************

223. spacer 19.16|8874577|32|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 9, identity: 0.719

cgaggcgcccacgctccccactgtttgaagaa	CRISPR spacer
tcggcgatccactcgccccactgtttgaagaa	Protospacer
. .*  ..**** * *****************

224. spacer 19.20|8874861|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 9, identity: 0.727

tgggccggcgtcctggagggtgccgcctggagg	CRISPR spacer
gcggccggcgccctggcgggtgccgctccgcgc	Protospacer
  ********.***** *********.. * *

225. spacer 19.20|8874861|33|NZ_CP017172|CRISPRCasFinder,CRT matches to GU911303 (Burkholderia phage KS5, complete genome) position: , mismatch: 9, identity: 0.727

tgggccggcgtcctggagggtgccgcctggagg	CRISPR spacer
gtcgccggcgtcctggacggtgcggccggcgcg	Protospacer
   ************** ***** *** * . *

226. spacer 19.22|8875002|32|NZ_CP017172|CRISPRCasFinder,CRT matches to CP054921 (Streptomyces sp. NA03103 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

atctccaggatgcagcaggcctacctcaacgc	CRISPR spacer
tcctccttgatgcagcaggcctaccgggcggc	Protospacer
 .****  *****************  .  **

227. spacer 19.26|8875286|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN224564 (Streptomyces phage Araceli, complete genome) position: , mismatch: 9, identity: 0.735

tgtcgtggcaccacagcagcaccgggttcttgat	CRISPR spacer
tctcgtggcaccacagcggcacctggaggtcgga	Protospacer
* ***************.***** **   *.*.

228. spacer 19.26|8875286|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH229863 (Streptomyces phage JackieB, complete genome) position: , mismatch: 9, identity: 0.735

tgtcgtggcaccacagcagcaccgggttcttgat	CRISPR spacer
tctcgtggcaccacagcggcacctggaggtcgga	Protospacer
* ***************.***** **   *.*.

229. spacer 19.26|8875286|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH229862 (Streptomyces phage Henoccus, complete genome) position: , mismatch: 9, identity: 0.735

tgtcgtggcaccacagcagcaccgggttcttgat	CRISPR spacer
tctcgtggcaccacagcggcacctggaggtcgga	Protospacer
* ***************.***** **   *.*.

230. spacer 19.27|8875357|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048425 (Rhizobium daejeonense strain KACC 13094 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.735

agcgcgagaatcgggcggcaccgtcgagttgccg	CRISPR spacer
gccacgagaagcgggcggcaacgtcgaggccgcg	Protospacer
. *.****** ********* ******* .  **

231. spacer 19.29|8875498|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 9, identity: 0.727

agagcggcttcgacggtcaactcggtgcttgcc	CRISPR spacer
tcttcctcttcgacggtcaaatcggtgattgcg	Protospacer
    *  ************* ****** ****

232. spacer 19.29|8875498|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020812 (Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.727

agagcggcttcgacggtcaactcggtgcttgcc	CRISPR spacer
ctcgcggcttcgacggtcaccccggtggcttcg	Protospacer
   **************** *.***** .* *

233. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054028 (Rhizobium sp. JKLM19E plasmid pPR19E01, complete sequence) position: , mismatch: 9, identity: 0.719

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcgtcgtccagtatcacgagggcctgggc	Protospacer
.  ***********.************.

234. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050104 (Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence) position: , mismatch: 9, identity: 0.719

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
gcgtcgtcggccaggatcacgaggttcatgcc	Protospacer
 ******** **** ********* .* * .

235. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050109 (Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence) position: , mismatch: 9, identity: 0.719

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
gcgtcgtcggccaggatcacgaggttcatgcc	Protospacer
 ******** **** ********* .* * .

236. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030761 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
gcgtcgtcggccaggatcacgaggttcatgcc	Protospacer
 ******** **** ********* .* * .

237. spacer 19.40|8876275|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_015188 (Acidiphilium multivorum AIU301 plasmid pACMV4, complete sequence) position: , mismatch: 9, identity: 0.719

atcgtaggcggcgcccccatcgcccccgagaa	CRISPR spacer
gaccagcgcggcgcccccaccgccgccgagga	Protospacer
. *  . ************.**** *****.*

238. spacer 19.41|8876344|37|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 9, identity: 0.757

gccgcgacctcgcgcgctacatgggcctggacttcgt	CRISPR spacer
gccgcgacctcgcgcgcggcatgggcggcgatctcac	Protospacer
***************** .*******   **..**..

239. spacer 19.41|8876344|37|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 9, identity: 0.757

gccgcgacctcgcgcgctacatgggcctggacttcgt	CRISPR spacer
gccgcgacctcgcgcgcggcatgggcggcgatctcac	Protospacer
***************** .*******   **..**..

240. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_015314 (Pseudonocardia dioxanivorans CB1190 plasmid pPSED01, complete sequence) position: , mismatch: 9, identity: 0.727

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
cgccggtgcggcggaggcggtgctggccagggg	Protospacer
 *.*.   *********** ** *********.

241. spacer 19.58|8877551|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP041652 (Streptomyces sp. RLB1-9 plasmid pRLB1-9.2, complete sequence) position: , mismatch: 9, identity: 0.735

agctggagctgacgctggatgccatggcggcgga	CRISPR spacer
gcgcgcgccagacgctggatgccgtggcggcgga	Protospacer
.  .* . * *************.**********

242. spacer 19.58|8877551|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KY290947 (Aeromonas phage 3, complete genome) position: , mismatch: 9, identity: 0.735

agctggagctgacgctggatgccatggcggcgga	CRISPR spacer
gggtgtccttgaggctggttgccatggcggcggt	Protospacer
.* **   .*** ***** **************

243. spacer 19.60|8877693|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022999 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence) position: , mismatch: 9, identity: 0.727

gcgtcgcggtgacgcccaggatgcgcgagttcg	CRISPR spacer
tcttcgcggtgacgcgcaggatgcccgtcacgg	Protospacer
 * ************ ******** **   . *

244. spacer 19.63|8877906|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035508 (Haematobacter massiliensis strain OT1 plasmid pOT1-8, complete sequence) position: , mismatch: 9, identity: 0.735

agatgtacgcgctcgccttcctctcgcgggctga	CRISPR spacer
ccctggcggcgctcgccttcctctcgccggctcc	Protospacer
   **   ******************* ****

245. spacer 19.65|8878049|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MT498055 (Arthrobacter phage Bumble, complete genome) position: , mismatch: 9, identity: 0.727

gacgtccccgtacgcggcccggtccgtcatcgg	CRISPR spacer
atccgccccgtacgcggcccggaccgacacggc	Protospacer
. *  ***************** *** **. *

246. spacer 19.67|8878189|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_020062 (Rhizobium tropici CIAT 899 plasmid pRtrCIAT899c, complete sequence) position: , mismatch: 9, identity: 0.735

cgagccgagcagcgagaacgtgacgccctctcat	CRISPR spacer
ggagccgagcagccagaacatgacgcccctcgcc	Protospacer
 ************ *****.********...  .

247. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
tacgccgcccacatcgccccggcgcccagcgc	Protospacer
  *  *****.**********.******   *

248. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
tacgccgcccacatcgccccggcgcccagcgc	Protospacer
  *  *****.**********.******   *

249. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019938 (Ketogulonicigenium robustum strain SPU_B003 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
ctgcgcgcccgcttcgccccgccgcccgaaca	Protospacer
 . ********* ******** *****. .*

250. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MT521993 (Gordonia phage RedWattleHog, complete genome) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
ccgagcacccgcatcaccccgacgcccatatg	Protospacer
 *  **.********.************...

251. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN586040 (Gordonia phage Stormageddon, complete genome) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
ccgagcacccgcatcaccccgacgcccatatg	Protospacer
 *  **.********.************...

252. spacer 19.69|8878332|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 9, identity: 0.719

acccgcgcccgcatcgccccgacgcccacgcc	CRISPR spacer
gcccccgcccgcatcgcctcgacggcggtatc	Protospacer
.*** *************.***** * ....*

253. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021028 (Rhizobium sp. TAL182 plasmid pRetTAL182d, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

254. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013503 (Rhizobium esperanzae strain N561 plasmid pRspN561c, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

255. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013509 (Rhizobium sp. N1341 plasmid pRspN1341d, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

256. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013520 (Rhizobium sp. N113 plasmid pRspN113c, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

257. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013493 (Rhizobium sp. N6212 plasmid pRspN6212c, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

258. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013516 (Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence) position: , mismatch: 9, identity: 0.719

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggcacgcg	Protospacer
...**** *** ************** *  .*

259. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KY494864 (Pseudomonas aeruginosa strain FFUP_PS_37 plasmid pJB37, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

260. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009975 (Pseudomonas putida S12 plasmid pTTS12, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

261. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039991 (Pseudomonas aeruginosa strain T2101 plasmid pBT2101, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

262. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_MN433457 (Pseudomonas aeruginosa strain PAB546 plasmid pNK546-KPC, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

263. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045003 (Pseudomonas aeruginosa strain PAG5 plasmid pPAG5, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

264. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045917 (Pseudomonas aeruginosa strain CF39S plasmid pCF39S, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

265. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MF344568 (Pseudomonas aeruginosa plasmid p727-IMP, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

266. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MF344569 (Pseudomonas aeruginosa plasmid p12939-PER, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

267. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to CP027478 (Pseudomonas koreensis strain P19E3 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

268. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP040126 (Pseudomonas aeruginosa strain PA298 plasmid pBM908, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

269. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015879 (Pseudomonas citronellolis strain SJTE-3 plasmid pRBL16, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

270. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016215 (Pseudomonas aeruginosa strain PA121617 plasmid pBM413, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

271. spacer 19.73|8878610|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KY883660 (Pseudomonas putida strain SY153 plasmid pSY153-MDR, complete sequence) position: , mismatch: 9, identity: 0.719

cgcgtagcccgcgctatccgccactggctcaa	CRISPR spacer
caagctctgcgcgacatccgccactggctcaa	Protospacer
*. *.  . **** .*****************

272. spacer 19.76|8878819|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_019519 (Agrobacterium phage 7-7-1, complete genome) position: , mismatch: 9, identity: 0.719

tggccgggcggtctcgggttcgccactgagtg	CRISPR spacer
gggccggtcggtgtcgggttcgcctgtttata	Protospacer
 ****** **** ***********  *  .*.

273. spacer 19.78|8878959|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027299 (Streptomyces sp. SGAir0924 plasmid unnamed_5) position: , mismatch: 9, identity: 0.719

cgcgagcacaacctggtgggctccttcgtcgc	CRISPR spacer
ctgctgcaccacctggtgggcttcttcggtgt	Protospacer
*    **** ************.***** .*.

274. spacer 19.81|8879169|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 9, identity: 0.743

cgccgcatctggaggggctgccggtgaaggcgtgg	CRISPR spacer
tcgcgcatctcgagggggtgccggtgaaggtggta	Protospacer
.  ******* ****** ************.*  .

275. spacer 19.81|8879169|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 9, identity: 0.743

cgccgcatctggaggggctgccggtgaaggcgtgg	CRISPR spacer
tcgcgcatctcgagggggtgccggtgaaggtggta	Protospacer
.  ******* ****** ************.*  .

276. spacer 19.82|8879241|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039697 (Novosphingobium sp. ABRDHK2 plasmid pABRDHK22, complete sequence) position: , mismatch: 9, identity: 0.735

cgtggtcctcgatcgcgttgtagcggattgcgat	CRISPR spacer
tgccgtcctcgacggcgttgtagcggatctcgcg	Protospacer
.*. ********. **************. **

277. spacer 19.86|8879531|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017753 (Cupriavidus sp. USMAHM13 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

ttgatgtgggtcttccgccagttcaccttccg	CRISPR spacer
gaggaattcgtcttccgtcagtttaccttccg	Protospacer
  *. .*  ********.*****.********

278. spacer 19.92|8879959|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026518 (Deinococcus sp. NW-56 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.727

acaaggcgcccacgtgccctgcctgccgctcta	CRISPR spacer
ttttggcgcccaggtgccctgccagccggacca	Protospacer
 .  ******** ********** ****  *.*

279. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032326 (Azospirillum brasilense strain MTCC4035 plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.735

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
cgcgccgagggtccaggccatgccgccgctcgac	Protospacer
 ************* *********** . . *

280. spacer 19.112|8881386|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023000 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence) position: , mismatch: 9, identity: 0.719

agggcgggcgggcagtcgcggacgtgggtgct	CRISPR spacer
gcggcgggcgtgcggtcgcggacgtgctgcgt	Protospacer
. ******** **.************     *

281. spacer 19.119|8881880|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029359 (Azospirillum sp. CFH 70021 plasmid unnamed4) position: , mismatch: 9, identity: 0.719

gccactcggtggagccctcggtggttgcccat	CRISPR spacer
agccttcggtgtcgccctcggtggttgccgcc	Protospacer
. * .******  ****************  .

282. spacer 19.120|8881949|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP042268 (Pseudomonas aeruginosa strain HOU1 plasmid pHOU1-1, complete sequence) position: , mismatch: 9, identity: 0.727

cgcggcaagctggaactgctgggctaccgcatg	CRISPR spacer
cagcgcgagctggaactgctgggccaccaggta	Protospacer
*.  **.*****************.***. .*.

283. spacer 20.4|9408406|30|NZ_CP017172|CRT matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.7

tcaaggccgcgagcgaggtgctcactcctg	CRISPR spacer
aggttgccgagagcgaggtgctcacaccac	Protospacer
  .  **** *************** **

284. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022775 (Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

285. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgcgcccagcgcacccggcagccatgtcgtc	Protospacer
********.***********.** ...*  ..

286. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP040937 (Hymenobacter sp. DG01 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
ggctgcccgccgcacccggcggcagcaacggc	Protospacer
*  .***** *************.***    .

287. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

288. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

289. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP023017 (Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

290. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

291. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

292. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

293. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
gcgctcccggcgctcccggcggcccgccggtc	Protospacer
**** ******** *********    .* ..

294. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

295. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

296. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

297. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022764 (Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

298. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022797 (Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

299. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to NZ_CP022758 (Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
accgatgcgccgaacccggcggcggcatgcac	Protospacer
.*  .. ** ** ***************** .

300. spacer 11.1|5618434|32|NZ_CP017172|CRISPRCasFinder matches to MK937591 (Microbacterium phage Cinna, complete genome) position: , mismatch: 10, identity: 0.688

gcgcgcccggcgcacccggcggcggcatgcct	CRISPR spacer
acctgctcggcgcacccggcgtcggcaaaagc	Protospacer
.* .**.************** ***** .  .

301. spacer 19.13|8874363|34|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 10, identity: 0.706

actacgcggtggtgcgcggacgcgacgcgcacgg	CRISPR spacer
gtgacgcggtggcgcgccgacgcgacgaccgacg	Protospacer
.. *********.**** *********  *.  *

302. spacer 19.14|8874434|37|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP033968 (Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.73

ggcgcagctgctccaccatcaccccctctacgttgat	CRISPR spacer
ggcgcagctgctccagcgtcaccccccgtgcacgcag	Protospacer
*************** *.********. *.*..  *

303. spacer 19.14|8874434|37|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP037902 (Cupriavidus metallidurans strain BS1 plasmid p1, complete sequence) position: , mismatch: 10, identity: 0.73

ggcgcagctgctccaccatcaccccctctacgttgat	CRISPR spacer
ggcgcagctgctccagcgtcaccccccgtgcacgcag	Protospacer
*************** *.********. *.*..  *

304. spacer 19.20|8874861|33|NZ_CP017172|CRISPRCasFinder,CRT matches to MT701591 (Burkholderia phage Mana, complete genome) position: , mismatch: 10, identity: 0.697

tgggccggcgtcctggagggtgccgcctggagg	CRISPR spacer
gtcgccggcgtcctggacggtgcggccggcgcc	Protospacer
   ************** ***** *** * .

305. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050092 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

306. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050081 (Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggg	Protospacer
.  **.********.************..  .

307. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050098 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

308. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050104 (Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

309. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049731 (Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggg	Protospacer
.  **.********.************..  .

310. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP053440 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

311. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018229 (Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

312. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025507 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

313. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016287 (Rhizobium leguminosarum strain Vaf10 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

314. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_HG938356 (Neorhizobium galegae bv. officinalis bv. officinalis str. HAMBI 1141 plasmid pHAMBI1141a, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcgtcgtccagtatcacgagagcctcggg	Protospacer
.  ***********.********.***..  .

315. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050109 (Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

316. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030761 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

317. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054022 (Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

318. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_012848 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggt	Protospacer
.  **.********.************..

319. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022666 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

320. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054032 (Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

321. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022565 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK01, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

322. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP053206 (Rhizobium leguminosarum bv. trifolii TA1 plasmid pRltTA1D, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggg	Protospacer
.  **.********.************..  .

323. spacer 19.31|8875640|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050086 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence) position: , mismatch: 10, identity: 0.688

tcgtcgtcgtccagcatcacgagggcccttta	CRISPR spacer
cgttcatcgtccagtatcacgagggcctcggc	Protospacer
.  **.********.************..

324. spacer 19.42|8876418|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MT664984 (Xanthomonas phage Xp12, complete genome) position: , mismatch: 10, identity: 0.688

cccagcagctccagcttgccccgccactgctc	CRISPR spacer
gccagcagctccagcttgcgcggcagggagta	Protospacer
 ****************** * ** .  . *

325. spacer 19.43|8876487|36|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_008043 (Ruegeria sp. TM1040 megaplasmid, complete sequence) position: , mismatch: 10, identity: 0.722

ttcttcatgccgccacccgggcgggctccagccggc	CRISPR spacer
cacgctctgccgccacccgcgcggcctccagcccgg	Protospacer
. * .. ************ **** ******** *

326. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KU160664 (Arthrobacter phage Salgado, complete genome) position: , mismatch: 10, identity: 0.697

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
ctcaataccggcggaggcgctgatgggctgggc	Protospacer
  . *...****************** * ***

327. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MF140418 (Arthrobacter phage LiSara, complete genome) position: , mismatch: 10, identity: 0.697

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
ctcaataccggcggaggcgctgatgggctgggc	Protospacer
  . *...****************** * ***

328. spacer 19.57|8877481|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KU160654 (Arthrobacter phage Laroye, complete genome) position: , mismatch: 10, identity: 0.697

agtcacgtcggcggaggcgctgatggccaggga	CRISPR spacer
ctcaataccggcggaggcgctgatgggctgggc	Protospacer
  . *...****************** * ***

329. spacer 19.58|8877551|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_008757 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP01, complete sequence) position: , mismatch: 10, identity: 0.706

agctggagctgacgctggatgccatggcggcgga	CRISPR spacer
cgttcagcctgccgctggttgccatggcggcgat	Protospacer
 *.* .. *** ****** *************.

330. spacer 19.58|8877551|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 10, identity: 0.706

--agctggagctgacgctggatgccatggcggcgga	CRISPR spacer
gcggcc--tgctgaccctgggtgccatggcggccct	Protospacer
  .**.   ****** ****.************

331. spacer 19.63|8877906|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 10, identity: 0.706

-agatgtacgcgctcgccttcctctcgcgggctga	CRISPR spacer
gcggcat-cgcgctcgccttcttcacgcgggcgag	Protospacer
  *...* *************.** ******* ..

332. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015585 (Roseomonas gilardii strain U14-5 plasmid 1, complete sequence) position: , mismatch: 10, identity: 0.688

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
gcggccagcgcgcgcagctccggcggcgagaa	Protospacer
 * ***.*** *************** ..  .

333. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021032 (Rhizobium sp. NXC14 plasmid pRspNXC14b, complete sequence) position: , mismatch: 10, identity: 0.688

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
ctcgccgccggtcgcagctccggcggctcgcg	Protospacer
...**** *** **************    .*

334. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024587 (Roseomonas sp. FDAARGOS_362 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.688

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
gcggccagcgcgcgcagctccggcggcgagaa	Protospacer
 * ***.*** *************** ..  .

335. spacer 19.71|8878471|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP006373 (Aureimonas sp. AU20 plasmid pAU20f, complete sequence) position: , mismatch: 10, identity: 0.688

tctgccggcgggcgcagctccggcggaagctg	CRISPR spacer
gctgccggcgggcgcaggtcccgccgcgatgc	Protospacer
 **************** *** ** * ...

336. spacer 19.82|8879241|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017300 (Rhodococcus sp. YL-1 plasmid pYLC1, complete sequence) position: , mismatch: 10, identity: 0.706

cgtggtcctcgatcgcgttgtagcggattgcgat	CRISPR spacer
ccgaggagtcgatcgcgttgttgcgaattgcgtc	Protospacer
*  .*   ************* ***.****** .

337. spacer 19.86|8879531|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN693118 (Marine virus AFVG_25M91, complete genome) position: , mismatch: 10, identity: 0.688

ttgatgtgggtcttccgccagttcaccttccg	CRISPR spacer
ttgatgtggggcttacgccagttgaagaaata	Protospacer
********** *** ******** *     ..

338. spacer 19.86|8879531|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN693323 (Marine virus AFVG_25M87, complete genome) position: , mismatch: 10, identity: 0.688

ttgatgtgggtcttccgccagttcaccttccg	CRISPR spacer
ttgatgtggggcttacgccagttgaagagatt	Protospacer
********** *** ******** *     .

339. spacer 19.96|8880242|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050094 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b4, complete sequence) position: , mismatch: 10, identity: 0.714

tggcgcgtcatcgcgtccgcggcccagtccgcgaa	CRISPR spacer
tggcgcatcatcgcggccgcggccctgcatgacgc	Protospacer
******.******** ********* *. .*  .

340. spacer 19.96|8880242|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_008379 (Rhizobium leguminosarum bv. viciae 3841 plasmid pRL9, complete sequence) position: , mismatch: 10, identity: 0.714

tggcgcgtcatcgcgtccgcggcccagtccgcgaa	CRISPR spacer
tggcgcatcatcgcggccgcggccctgcatgacgc	Protospacer
******.******** ********* *. .*  .

341. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN586025 (Mycobacterium phage Mdavu, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

342. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KT281789 (Mycobacterium phage Enkosi, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

343. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH020245 (Mycobacterium phage SgtBeansprout, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

344. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KX808132 (Mycobacterium phage Amelie, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

345. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH399770 (Mycobacterium phage Biglebops, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

346. spacer 19.106|8880956|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MF919518 (Mycobacterium phage LilPharaoh, complete genome) position: , mismatch: 10, identity: 0.706

agcgccgagggtcccggccatgccgcgagcagta	CRISPR spacer
catttcgagggtcgcggccatgccgccaggtgtg	Protospacer
 .. .******** ************ **  **.

347. spacer 19.109|8881171|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014802 (Salipiger profundus strain JLT2016 plasmid pTPRO6, complete sequence) position: , mismatch: 10, identity: 0.706

-------aggcagtcatccacaccgctgggacgttgggcga	CRISPR spacer
ttcctcgaga-------ccatgccgctgggacgttgggcga	Protospacer
       **.       ***..*******************

348. spacer 19.112|8881386|32|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018075 (Streptomyces venezuelae strain NRRL B-65442 plasmid, complete sequence) position: , mismatch: 10, identity: 0.688

agggcgggcgggcagtcgcggacgtgggtgct	CRISPR spacer
agggcgggcggcccgtcgcggacagcgtccac	Protospacer
*********** * *********.  * .  .

349. spacer 19.123|8882160|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049358 (Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

tggacgcgcccgccgtgagcagcaccaggtcct	CRISPR spacer
acgacgcccccgccgtgagcggcaccgcgcagc	Protospacer
  ***** ************.*****. *.  .

350. spacer 19.123|8882160|33|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031159 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence) position: , mismatch: 10, identity: 0.697

tggacgcgcccgccgtgagcagcaccaggtcct	CRISPR spacer
acgacgcccccgccgtgagcggcaccgcgcagc	Protospacer
  ***** ************.*****. *.  .

351. spacer 19.4|8873727|33|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 11, identity: 0.667

cacgacggatgcgcctgcccgcaggcacgtgtg	CRISPR spacer
aggaccggctgcgcctgcccgccggcacgcacc	Protospacer
 . . *** ************* ******...

352. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN234182 (Mycobacterium phage Geraldini, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgagctcgac	Protospacer
 . .*********.********** *****..  .

353. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MN234198 (Mycobacterium phage Zavala, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgagctcgac	Protospacer
 . .*********.********** *****..  .

354. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MK460247 (Mycobacterium phage YoureAdopted, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgagctcgac	Protospacer
 . .*********.********** *****..  .

355. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH513977 (Mycobacterium phage Mynx, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgagctcgac	Protospacer
 . .*********.********** *****..  .

356. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MH371113 (Mycobacterium phage Beezoo, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgagctcgac	Protospacer
 . .*********.********** *****..  .

357. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to MF377440 (Mycobacterium phage Bella96, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgaggtcact	Protospacer
 . .*********.********** **** .. .*

358. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KX657796 (Mycobacterium phage Urkel, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgaggtcact	Protospacer
 . .*********.********** **** .. .*

359. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KX657794 (Mycobacterium phage SamuelLPlaqson, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgaggtcact	Protospacer
 . .*********.********** **** .. .*

360. spacer 19.34|8875851|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KX657795 (Mycobacterium phage DrHayes, complete genome) position: , mismatch: 11, identity: 0.686

ctcgcacgggcgaactggcgctgtacgagcctctt	CRISPR spacer
gcgacacgggcgagctggcgctgttcgaggtcact	Protospacer
 . .*********.********** **** .. .*

361. spacer 19.62|8877835|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022195 (Yangia pacifica strain YSBP01 plasmid unnamed5, complete sequence) position: , mismatch: 11, identity: 0.676

tgcccagcaccacgaccggcgggccagctctctt	CRISPR spacer
ggcccagcacctcggccggcgggccgtcggcgcg	Protospacer
 ********** **.**********. *  . .

362. spacer 19.62|8877835|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to JN699011 (Mycobacterium phage Stinger, complete genome) position: , mismatch: 11, identity: 0.676

tgcccagcaccacgaccggcgggccagctctctt	CRISPR spacer
gccccagcaccgtgaccggcgggccacccgagcc	Protospacer
  *********..************* *.   ..

363. spacer 19.62|8877835|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NC_011044 (Mycobacterium phage Nigel, complete genome) position: , mismatch: 11, identity: 0.676

tgcccagcaccacgaccggcgggccagctctctt	CRISPR spacer
gccccagcaccgtgaccggcgggccaccggagcc	Protospacer
  *********..************* *    ..

364. spacer 19.62|8877835|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KR080200 (Mycobacterium phage AlanGrant, complete genome) position: , mismatch: 11, identity: 0.676

tgcccagcaccacgaccggcgggccagctctctt	CRISPR spacer
gccccagcaccgtgaccggcgggccaccggagcc	Protospacer
  *********..************* *    ..

365. spacer 19.62|8877835|34|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to KR080194 (Mycobacterium phage Vincenzo, complete genome) position: , mismatch: 11, identity: 0.676

tgcccagcaccacgaccggcgggccagctctctt	CRISPR spacer
gccccagcaccgtgaccggcgggccaccggagcc	Protospacer
  *********..************* *    ..

366. spacer 19.13|8874363|34|NZ_CP017172|CRISPRCasFinder,CRT matches to NZ_CP024895 (Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence) position: , mismatch: 12, identity: 0.647

actacgcggtggtgcgcggacgcgacgcgcacgg	CRISPR spacer
acttcgcggtggcgcgcggacgcgggagctggac	Protospacer
*** ********.***********. .  .. .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

2061689 : 2108156

Acanthocystis_turfacea_Chlorella_virus(25.0%)

protease,transposase

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_140873837.1\|2061689_2062517_-\|protease	protease	NA	NA	NA	NA
WP_174259226.1\|2063530_2066635_-	tetratricopeptide repeat protein	M1HTZ5	Acanthocystis_turfacea_Chlorella_virus	4.3e-07	28.3
WP_140873839.1\|2067060_2071890_+	DNA/RNA non-specific endonuclease	NA	NA	NA	NA
WP_161604861.1\|2072003_2072177_+	hypothetical protein	NA	NA	NA	NA
WP_161604862.1\|2072315_2072489_+	hypothetical protein	NA	NA	NA	NA
WP_140788943.1\|2072473_2072665_+	hypothetical protein	NA	NA	NA	NA
WP_161604863.1\|2073502_2073787_-	hypothetical protein	NA	NA	NA	NA
WP_140788944.1\|2073755_2074004_-\|transposase	transposase	NA	NA	NA	NA
WP_140788947.1\|2074321_2074825_-	hypothetical protein	NA	NA	NA	NA
WP_174259149.1\|2076012_2076258_+	hypothetical protein	NA	NA	NA	NA
WP_161604864.1\|2076769_2078065_-	serine hydrolase	A0A1V0SLG8	Klosneuvirus	1.4e-12	29.7
WP_140788949.1\|2079426_2079717_-	hypothetical protein	NA	NA	NA	NA
WP_140878265.1\|2080842_2083284_-	Ig-like domain-containing protein	NA	NA	NA	NA
WP_140873841.1\|2083989_2084889_-	hypothetical protein	NA	NA	NA	NA
WP_140800638.1\|2085766_2086159_+	hypothetical protein	NA	NA	NA	NA
WP_140788952.1\|2086504_2087428_+	hypothetical protein	NA	NA	NA	NA
WP_140873843.1\|2087636_2088350_+	hypothetical protein	NA	NA	NA	NA
WP_020478490.1\|2088569_2089148_-	pirin family protein	NA	NA	NA	NA
WP_140797673.1\|2089525_2090356_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140853429.1\|2090391_2091423_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140853493.1\|2091419_2091980_-\|transposase	transposase	NA	NA	NA	NA
WP_140788956.1\|2093446_2093812_-	gas vesicle protein	NA	NA	NA	NA
WP_140788957.1\|2093846_2094173_-	gas vesicle protein K	NA	NA	NA	NA
WP_011552834.1\|2094221_2094443_-	gas vesicle protein	NA	NA	NA	NA
WP_140788959.1\|2094439_2094721_-	gas vesicle protein GvpG	NA	NA	NA	NA
WP_140788961.1\|2094717_2095527_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140788962.1\|2095557_2095782_-	gas vesicle structural protein GvpA	NA	NA	NA	NA
WP_140788963.1\|2095789_2096557_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140796389.1\|2096553_2097372_-	GvpL/GvpF family gas vesicle protein	NA	NA	NA	NA
WP_140797676.1\|2097392_2099528_-	CDC48 family AAA ATPase	A0A2K9R7H3	Dishui_lake_phycodnavirus	1.5e-48	48.0
WP_140788966.1\|2099524_2100049_-	Hsp20/alpha crystallin family protein	NA	NA	NA	NA
WP_140873845.1\|2100390_2101677_+	PDZ domain-containing protein	NA	NA	NA	NA
WP_140873847.1\|2102048_2102432_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140878268.1\|2102489_2103050_+\|transposase	transposase	NA	NA	NA	NA
WP_161607075.1\|2103340_2107081_-	HYR domain-containing protein	NA	NA	NA	NA
WP_140788974.1\|2107643_2108156_+\|transposase	transposase	NA	NA	NA	NA

DBSCAN-SWA_2

2115934 : 2170024

Pseudomonas_phage(40.0%)

portal,transposase,terminase,head

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140853453.1\|2115934_2116462_+\|transposase	transposase	NA	NA	NA	NA
WP_140788984.1\|2116859_2117168_+	hypothetical protein	NA	NA	NA	NA
WP_140788986.1\|2118237_2119455_+	HlyD family efflux transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_140873855.1\|2119457_2122187_+	ATP-binding cassette domain-containing protein	A0A076FI99	Aureococcus_anophage	5.6e-19	27.7
WP_140788990.1\|2122183_2124295_+	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	4.0e-09	29.1
WP_140853454.1\|2124291_2125791_+	TolC family protein	NA	NA	NA	NA
WP_140788994.1\|2125797_2127546_+	hypothetical protein	NA	NA	NA	NA
WP_140797690.1\|2127554_2128565_+	phosphotransferase	NA	NA	NA	NA
WP_140873857.1\|2129323_2129851_+\|transposase	transposase	NA	NA	NA	NA
WP_140873859.1\|2130229_2131258_-	AAA family ATPase	H2BD62	Pseudomonas_phage	1.7e-93	52.6
WP_140873861.1\|2133401_2133878_+	SgcJ/EcaC family oxidoreductase	NA	NA	NA	NA
WP_140873864.1\|2136827_2138333_+	hypothetical protein	NA	NA	NA	NA
WP_140873866.1\|2138511_2139579_-	hypothetical protein	NA	NA	NA	NA
WP_161607076.1\|2139686_2141342_-	DUF262 domain-containing protein	NA	NA	NA	NA
WP_140873870.1\|2141535_2142003_-	hypothetical protein	NA	NA	NA	NA
WP_161607077.1\|2142066_2143371_-	hypothetical protein	NA	NA	NA	NA
WP_140873874.1\|2143457_2146943_-	AAA family ATPase	NA	NA	NA	NA
WP_161607078.1\|2147030_2147765_-	DUF4194 domain-containing protein	NA	NA	NA	NA
WP_161607079.1\|2147764_2149231_-	hypothetical protein	NA	NA	NA	NA
WP_161607080.1\|2149923_2150163_-	hypothetical protein	NA	NA	NA	NA
WP_140878271.1\|2150621_2151212_+	RDD family protein	NA	NA	NA	NA
WP_140878273.1\|2151304_2153179_+	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_140878275.1\|2153244_2153655_-	cell wall protein	NA	NA	NA	NA
WP_161607081.1\|2153738_2154578_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140873881.1\|2154732_2155596_-	hypothetical protein	NA	NA	NA	NA
WP_140873883.1\|2155871_2156690_-	hypothetical protein	NA	NA	NA	NA
WP_140873887.1\|2160981_2162061_-\|head	head morphogenesis protein	NA	NA	NA	NA
WP_140873889.1\|2162041_2162323_-	hypothetical protein	NA	NA	NA	NA
WP_140873891.1\|2162319_2164119_-\|portal	phage portal protein	A0A0U3E050	Pseudomonas_phage	1.6e-51	30.9
WP_140873893.1\|2164115_2164319_-	hypothetical protein	NA	NA	NA	NA
WP_140873896.1\|2166576_2167764_+	DNA integrity scanning protein DisA nucleotide-binding domain protein	NA	NA	NA	NA
WP_140873898.1\|2167836_2168400_-\|terminase	terminase	NA	NA	NA	NA
WP_140853429.1\|2168465_2169497_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_161607082.1\|2169493_2170024_-\|transposase	transposase	NA	NA	NA	NA

DBSCAN-SWA_3

2321632 : 2332257

Bacillus_thuringiensis_phage(14.29%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140873987.1\|2321632_2324485_+	response regulator	Q56AR1	Bacillus_thuringiensis_phage	3.0e-07	31.3
WP_140797760.1\|2324534_2325530_+\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD	A0A0R6PI74	Moraxella_phage	2.2e-74	46.3
WP_140789208.1\|2325544_2326396_+	16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))- dimethyltransferase RsmA	E4ZFQ0	Streptococcus_phage	6.4e-14	33.7
WP_043710562.1\|2326403_2326682_-	hypothetical protein	NA	NA	NA	NA
WP_011552138.1\|2326892_2327537_+	deoxynucleoside kinase	A0A288TXV5	Enterococcus_phage	2.6e-15	32.8
WP_140873989.1\|2327701_2328619_+	3-methyl-2-oxobutanoate hydroxymethyltransferase	M4QNT1	Ostreococcus_lucimarinus_virus	9.5e-48	38.4
WP_140873991.1\|2328621_2329500_+	pantoate--beta-alanine ligase	NA	NA	NA	NA
WP_140789216.1\|2329496_2329985_+	SsrA-binding protein SmpB	W5RAM5	Staphylococcus_phage	2.1e-30	47.2
WP_140873993.1\|2330018_2330540_+	stringent starvation protein B	NA	NA	NA	NA
WP_140797762.1\|2330547_2332257_-	protein kinase	A0A1E1EXF7	Acanthamoeba_castellanii_mimivirus	4.9e-13	29.0

DBSCAN-SWA_4

3155144 : 3235983

Bacillus_phage(30.0%)

protease,transposase,integrase,tRNA

attL 3164058:3164074|attR 3247866:3247882

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140874466.1\|3155144_3155864_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_140874468.1\|3155860_3156481_-	trypsin-like peptidase domain-containing protein	NA	NA	NA	NA
WP_140878327.1\|3156500_3158246_-	DNA polymerase/3'-5' exonuclease PolX	NA	NA	NA	NA
WP_140790287.1\|3158324_3158642_+	Rieske 2Fe-2S domain-containing protein	NA	NA	NA	NA
WP_140878329.1\|3158881_3159349_+	MogA/MoaB family molybdenum cofactor biosynthesis protein	NA	NA	NA	NA
WP_140854061.1\|3159514_3161554_+	M20/M25/M40 family metallo-hydrolase	NA	NA	NA	NA
WP_140874470.1\|3161660_3162017_+	GatB/YqeY domain-containing protein	NA	NA	NA	NA
WP_140874472.1\|3162156_3163062_+	TIGR02757 family protein	NA	NA	NA	NA
WP_174258762.1\|3163150_3164716_+	response regulator	NA	NA	NA	NA
3164058:3164074	attL	NA	NA	NA	NA
WP_174258763.1\|3164712_3165867_+	hypothetical protein	NA	NA	NA	NA
WP_140874476.1\|3165879_3167367_-	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_140874478.1\|3167460_3168771_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_140790300.1\|3168777_3169536_-	TonB family protein	NA	NA	NA	NA
WP_090488889.1\|3169703_3170420_-	response regulator transcription factor	W8CYM9	Bacillus_phage	6.3e-31	36.4
WP_140874480.1\|3170416_3172246_-	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	9.5e-15	26.9
WP_140790303.1\|3172246_3173179_+	pyridoxal-phosphate dependent enzyme	NA	NA	NA	NA
WP_140790304.1\|3173201_3173972_-	hypothetical protein	NA	NA	NA	NA
WP_140874482.1\|3174118_3176533_-	ABC transporter permease	NA	NA	NA	NA
WP_140790306.1\|3176683_3177364_-	hypothetical protein	NA	NA	NA	NA
WP_174259260.1\|3177484_3180517_-	response regulator	W8CYF6	Bacillus_phage	3.0e-29	31.7
WP_140798073.1\|3180877_3181942_+	4-hydroxyphenylpyruvate dioxygenase	NA	NA	NA	NA
WP_174259050.1\|3181996_3183310_+	homogentisate 1,2-dioxygenase	NA	NA	NA	NA
WP_140798074.1\|3183317_3183698_+	Rieske 2Fe-2S domain-containing protein	NA	NA	NA	NA
WP_140790310.1\|3183707_3185114_-	MATE family efflux transporter	NA	NA	NA	NA
WP_140874484.1\|3185537_3186365_-	trypsin-like peptidase domain-containing protein	NA	NA	NA	NA
WP_140790312.1\|3186368_3187166_-\|protease	protease	NA	NA	NA	NA
WP_140874486.1\|3187593_3188772_+	hypothetical protein	NA	NA	NA	NA
WP_174259261.1\|3189104_3190226_+	hypothetical protein	NA	NA	NA	NA
WP_140790317.1\|3190353_3191133_-	TetR/AcrR family transcriptional regulator C-terminal domain-containing protein	NA	NA	NA	NA
WP_140798080.1\|3191299_3193549_+	ATP-binding cassette domain-containing protein	A0A1B1IVR3	uncultured_Mediterranean_phage	9.6e-126	33.2
WP_140874490.1\|3193754_3198422_-	LLM class flavin-dependent oxidoreductase	A0A2K9KZV5	Tupanvirus	3.3e-19	34.2
WP_140790322.1\|3198462_3199305_-	alpha/beta hydrolase	NA	NA	NA	NA
WP_140874492.1\|3199301_3205565_-	SDR family oxidoreductase	D0R7J2	Paenibacillus_phage	6.5e-47	36.0
WP_174259051.1\|3205692_3207210_-	mechanosensitive ion channel	NA	NA	NA	NA
WP_140790327.1\|3207268_3208303_+	DNA polymerase III subunit delta'	NA	NA	NA	NA
WP_140790329.1\|3208299_3209634_+	DNA polymerase III subunit delta	NA	NA	NA	NA
WP_140790330.1\|3209645_3210104_+	hypothetical protein	NA	NA	NA	NA
WP_140854098.1\|3210128_3210929_-	NRDE family protein	NA	NA	NA	NA
WP_140854100.1\|3211044_3213153_+\|tRNA	methionine--tRNA ligase	A0A2K9L3E6	Tupanvirus	5.2e-57	28.8
WP_140874494.1\|3213154_3214132_+	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_140790337.1\|3214128_3214905_+	YchF/TatD family DNA exonuclease	NA	NA	NA	NA
WP_140874496.1\|3214891_3216874_-	DUF4388 domain-containing protein	NA	NA	NA	NA
WP_140796447.1\|3216882_3218334_-	DNA-binding protein	NA	NA	NA	NA
WP_140790341.1\|3218381_3219521_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_140790343.1\|3219679_3220048_-	hypothetical protein	NA	NA	NA	NA
WP_140790345.1\|3220070_3221666_-	FAD-dependent monooxygenase	NA	NA	NA	NA
WP_140790347.1\|3221896_3222172_+	hypothetical protein	NA	NA	NA	NA
WP_140790349.1\|3222305_3222959_-\|protease	MprA protease, GlyGly-CTERM protein-sorting domain-containing form	NA	NA	NA	NA
WP_140874498.1\|3223038_3225906_+	N-acetylmuramoyl-L-alanine amidase	NA	NA	NA	NA
WP_011552882.1\|3226000_3227011_+	type I glyceraldehyde-3-phosphate dehydrogenase	NA	NA	NA	NA
WP_140790353.1\|3227050_3228238_+	phosphoglycerate kinase	NA	NA	NA	NA
WP_140862107.1\|3228277_3229048_+	triose-phosphate isomerase	NA	NA	NA	NA
WP_140874499.1\|3229143_3229542_+	preprotein translocase subunit SecG	NA	NA	NA	NA
WP_140874500.1\|3229774_3230989_-\|integrase	tyrosine-type recombinase/integrase	Q9T1P3	Pseudomonas_phage	4.7e-18	26.8
WP_140874501.1\|3230985_3231237_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140874502.1\|3231233_3232769_-	ATP-binding protein	I6NPA6	Burkholderia_phage	2.2e-12	33.1
WP_140874503.1\|3232765_3233881_-	hypothetical protein	NA	NA	NA	NA
WP_140874505.1\|3234141_3234372_-	hypothetical protein	NA	NA	NA	NA
WP_140853429.1\|3234394_3235426_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	27.6
WP_140853493.1\|3235422_3235983_-\|transposase	transposase	NA	NA	NA	NA
3247866:3247882	attR	NA	NA	NA	NA

DBSCAN-SWA_5

3680154 : 3737132

Clostridium_phage(16.67%)

protease,transposase,integrase

attL 3721075:3721091|attR 3744636:3744652

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140874785.1\|3680154_3681495_+\|protease	M6 family metalloprotease domain-containing protein	A0A1L2BY89	Clostridium_phage	3.4e-30	29.9
WP_140874789.1\|3681933_3682821_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140790879.1\|3682940_3683345_+	RidA family protein	NA	NA	NA	NA
WP_140874791.1\|3683515_3685840_-	ethanolamine ammonia-lyase subunit EutB	NA	NA	NA	NA
WP_002640507.1\|3686092_3686986_+	1,4-dihydroxy-2-naphthoyl-CoA synthase	NA	NA	NA	NA
WP_140790883.1\|3687077_3687482_+	hypothetical protein	NA	NA	NA	NA
WP_174259277.1\|3687498_3688173_-	hemolysin III family protein	NA	NA	NA	NA
WP_140790885.1\|3688605_3689604_+	hypothetical protein	NA	NA	NA	NA
WP_140874795.1\|3689751_3693063_+	hypothetical protein	NA	NA	NA	NA
WP_140790889.1\|3693219_3695331_+	peptidase M13	E3T4I7	Cafeteria_roenbergensis_virus	5.3e-86	31.4
WP_140874797.1\|3695384_3695609_+	hypothetical protein	NA	NA	NA	NA
WP_174258790.1\|3695633_3697271_-	fumarate hydratase	NA	NA	NA	NA
WP_140874799.1\|3697482_3698835_+	OmpA family protein	NA	NA	NA	NA
WP_140874801.1\|3699081_3699714_+	hypothetical protein	NA	NA	NA	NA
WP_140854445.1\|3699756_3701415_-	hypothetical protein	NA	NA	NA	NA
WP_140874803.1\|3701889_3702621_-	hypothetical protein	NA	NA	NA	NA
WP_140790898.1\|3702858_3703440_+	hypothetical protein	NA	NA	NA	NA
WP_140874805.1\|3703506_3704421_-	hypothetical protein	NA	NA	NA	NA
WP_140800684.1\|3704490_3705684_-	J domain-containing protein	NA	NA	NA	NA
WP_140878342.1\|3705803_3706607_-	hypothetical protein	NA	NA	NA	NA
WP_140790901.1\|3706811_3707756_+	DUF808 family protein	NA	NA	NA	NA
WP_140874807.1\|3707805_3708621_-	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_174259278.1\|3708617_3709646_-	NADP-dependent oxidoreductase	NA	NA	NA	NA
WP_140790906.1\|3709816_3710887_+\|protease	FtsH protease activity modulator HflK	NA	NA	NA	NA
WP_140790908.1\|3710883_3711822_+\|protease	protease modulator HflC	NA	NA	NA	NA
WP_140874809.1\|3711742_3712519_+	cytochrome P450	NA	NA	NA	NA
WP_140874811.1\|3712587_3713946_-	general secretion pathway protein GspE	NA	NA	NA	NA
WP_140874814.1\|3714025_3715648_-	hypothetical protein	NA	NA	NA	NA
WP_140790916.1\|3716160_3717084_+	endonuclease/exonuclease/phosphatase family protein	NA	NA	NA	NA
WP_140790918.1\|3717056_3717752_+	hypothetical protein	NA	NA	NA	NA
WP_140790920.1\|3717807_3718362_-	hypothetical protein	NA	NA	NA	NA
WP_140790922.1\|3719292_3719601_+	hypothetical protein	NA	NA	NA	NA
WP_140790924.1\|3719826_3720117_+	hypothetical protein	NA	NA	NA	NA
WP_140878344.1\|3720086_3720410_-	serine hydrolase	NA	NA	NA	NA
WP_140874816.1\|3720575_3720821_-	hypothetical protein	NA	NA	NA	NA
3721075:3721091	attL	NA	NA	NA	NA
WP_140874818.1\|3721107_3721764_-	DUF664 domain-containing protein	NA	NA	NA	NA
WP_140874820.1\|3722055_3725766_-	ATP-dependent RNA helicase HrpA	A0A1V0SBU4	Catovirus	8.3e-42	27.1
WP_161607097.1\|3725813_3726149_+\|transposase	transposase	NA	NA	NA	NA
WP_161607098.1\|3726504_3727023_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_161607099.1\|3726943_3727618_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_140790937.1\|3727607_3727976_-	acyl carrier protein	K4FB26	Cronobacter_phage	8.9e-05	40.8
WP_140790939.1\|3728079_3728358_+	hypothetical protein	NA	NA	NA	NA
WP_140874828.1\|3728726_3730049_+	AHH domain-containing protein	NA	NA	NA	NA
WP_174259279.1\|3730052_3730625_+	hypothetical protein	NA	NA	NA	NA
WP_140874830.1\|3730821_3731379_+	hypothetical protein	NA	NA	NA	NA
WP_161607100.1\|3731386_3731530_+	hypothetical protein	NA	NA	NA	NA
WP_140790946.1\|3731715_3732579_+	DUF2381 family protein	NA	NA	NA	NA
WP_140790948.1\|3732575_3734369_+	protein kinase	A0A146JFA3	Tokyovirus	7.4e-12	25.6
WP_140796468.1\|3734526_3735681_+	protein kinase	M1PCM5	Moumouvirus	3.3e-05	24.1
WP_140878346.1\|3735995_3737132_+\|integrase	site-specific integrase	NA	NA	NA	NA
3744636:3744652	attR	NA	NA	NA	NA

DBSCAN-SWA_6

3754247 : 3765883

Dinoroseobacter_phage(33.33%)

portal,tail,capsid,transposase,head,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140874862.1\|3754247_3754724_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_140874864.1\|3754716_3756132_+	ATP/GTP-binding protein	A0A1V0DY66	Dinoroseobacter_phage	9.2e-58	37.0
WP_140874867.1\|3756158_3757487_+\|portal	phage portal protein	M1PLL1	Streptococcus_phage	1.5e-09	26.8
WP_140874870.1\|3757522_3758356_+\|head,protease	HK97 family phage prohead protease	A0A142K631	Streptomyces_phage	1.6e-09	31.7
WP_140874873.1\|3758352_3759441_+\|capsid	phage major capsid protein	NA	NA	NA	NA
WP_140874876.1\|3759452_3759866_+	hypothetical protein	NA	NA	NA	NA
WP_140874878.1\|3759956_3760613_+	hypothetical protein	NA	NA	NA	NA
WP_140799309.1\|3760612_3760936_+	hypothetical protein	NA	NA	NA	NA
WP_140874880.1\|3760935_3761355_+	hypothetical protein	NA	NA	NA	NA
WP_140874883.1\|3761391_3761808_+	hypothetical protein	NA	NA	NA	NA
WP_140874885.1\|3761816_3762242_+	hypothetical protein	NA	NA	NA	NA
WP_140874887.1\|3762241_3762898_+	hypothetical protein	NA	NA	NA	NA
WP_140793746.1\|3762929_3763283_+\|tail	phage tail protein	NA	NA	NA	NA
WP_174259281.1\|3763504_3765883_+\|tail	phage tail protein	NA	NA	NA	NA

DBSCAN-SWA_7

4303180 : 4324484

Pseudomonas_phage(33.33%)

terminase,tail,capsid

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_161607113.1\|4303180_4303753_+\|terminase	terminase small subunit	NA	NA	NA	NA
WP_161607114.1\|4303745_4305017_+	hypothetical protein	A0A1B1IN95	uncultured_Mediterranean_phage	2.9e-111	52.5
WP_140875235.1\|4305016_4305517_+	Mov34/MPN/PAD-1 family protein	NA	NA	NA	NA
WP_140875237.1\|4305516_4305726_+	hypothetical protein	NA	NA	NA	NA
WP_140875238.1\|4305727_4307224_+	DUF4055 domain-containing protein	A0A2D2W2J8	Stenotrophomonas_phage	9.0e-112	48.0
WP_140875240.1\|4307253_4307592_+	hypothetical protein	NA	NA	NA	NA
WP_140875242.1\|4307592_4308810_+\|capsid	minor capsid protein	A0A0S0N1M5	Pseudomonas_phage	8.7e-81	42.8
WP_140875244.1\|4308840_4309596_+	hypothetical protein	NA	NA	NA	NA
WP_140875246.1\|4309763_4310699_+\|capsid	phage major capsid protein	A0A0S0N8I6	Pseudomonas_phage	1.7e-92	59.3
WP_140875248.1\|4310769_4311228_+	hypothetical protein	NA	NA	NA	NA
WP_140875251.1\|4311252_4311747_+	hypothetical protein	NA	NA	NA	NA
WP_140875253.1\|4311743_4312118_+	hypothetical protein	NA	NA	NA	NA
WP_140875255.1\|4312114_4312579_+	HK97 gp10 family phage protein	S4SIM9	Salmonella_phage	1.2e-19	38.5
WP_140875257.1\|4312575_4313001_+	hypothetical protein	NA	NA	NA	NA
WP_140875259.1\|4313032_4314172_+	hypothetical protein	A0A0S0MV10	Pseudomonas_phage	3.9e-67	41.8
WP_140875261.1\|4314219_4314660_+	hypothetical protein	NA	NA	NA	NA
WP_140875263.1\|4314680_4314971_+	hypothetical protein	NA	NA	NA	NA
WP_140875266.1\|4314985_4315444_-	hypothetical protein	NA	NA	NA	NA
WP_140875268.1\|4315531_4319221_+\|tail	phage tail tape measure protein	A0A1V0DYA9	Dinoroseobacter_phage	9.7e-59	41.8
WP_140875270.1\|4319268_4319652_-	hypothetical protein	NA	NA	NA	NA
WP_140875272.1\|4319651_4320239_-	hypothetical protein	NA	NA	NA	NA
WP_161607115.1\|4321001_4321730_+	restriction endonuclease	NA	NA	NA	NA
WP_140875276.1\|4321810_4322401_+\|tail	phage tail protein	K7PKL8	Enterobacterial_phage	5.2e-07	41.6
WP_140875278.1\|4323033_4323219_+	hypothetical protein	NA	NA	NA	NA
WP_140875280.1\|4323788_4324484_+\|tail	phage minor tail protein L	J9Q7Y5	Salmonella_phage	6.1e-55	47.6

DBSCAN-SWA_8

5613854 : 5663577

Klosneuvirus(12.5%)

transposase,integrase,tail,tRNA

attL 5633208:5633224|attR 5635566:5635582

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140875948.1\|5613854_5617751_-\|tRNA	valine--tRNA ligase	A0A1V0SK04	Klosneuvirus	8.2e-157	40.7
WP_140793067.1\|5617816_5619082_-	response regulator	NA	NA	NA	NA
WP_140793068.1\|5619198_5620014_-	chemotaxis protein CheW	NA	NA	NA	NA
WP_140798914.1\|5620064_5621438_+	diguanylate cyclase	A0A127AWB9	Bacillus_phage	1.2e-17	33.5
WP_140793072.1\|5621441_5621834_-	demethoxyubiquinone hydroxylase family protein	NA	NA	NA	NA
WP_161606781.1\|5621983_5623501_+	hybrid histidine protein kinase/response regulator SinK	Q8QKV7	Ectocarpus_siliculosus_virus	9.4e-08	21.7
WP_140875950.1\|5623497_5624580_+	signal integration modulator SinM	NA	NA	NA	NA
WP_140875952.1\|5624757_5626401_-	chaperonin GroEL	A0A240F779	uncultured_virus	1.1e-166	58.2
WP_002639463.1\|5626569_5626926_-	response regulator	NA	NA	NA	NA
WP_174259322.1\|5627018_5628089_+	metallopeptidase family protein	NA	NA	NA	NA
WP_140875956.1\|5628042_5629020_-	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_140875958.1\|5629066_5629765_+	WHG domain-containing protein	NA	NA	NA	NA
WP_140875960.1\|5630146_5630926_+	hypothetical protein	NA	NA	NA	NA
WP_161607122.1\|5632678_5633224_+\|transposase	transposase family protein	NA	NA	NA	NA
5633208:5633224	attL	NA	NA	NA	NA
WP_140878425.1\|5633465_5634743_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
WP_140875965.1\|5634739_5635552_+	AAA family ATPase	NA	NA	NA	NA
WP_140875967.1\|5635845_5636037_-	hypothetical protein	NA	NA	NA	NA
5635566:5635582	attR	NA	NA	NA	NA
WP_161607123.1\|5636033_5636492_-\|transposase	transposase	NA	NA	NA	NA
WP_140875971.1\|5637233_5640359_+	hypothetical protein	NA	NA	NA	NA
WP_140875973.1\|5640355_5640817_+	response regulator	NA	NA	NA	NA
WP_140875975.1\|5640813_5642055_+	response regulator	NA	NA	NA	NA
WP_140875977.1\|5643255_5644422_+	protein kinase	A0A0U2U263	Niemeyer_virus	2.9e-09	28.9
WP_020479164.1\|5644444_5644792_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_140875979.1\|5644928_5645231_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_140798970.1\|5645379_5647332_+	protein kinase	A0A2R8FF19	Brazilian_cedratvirus	4.9e-09	26.9
WP_140875981.1\|5647341_5648268_+	DUF2381 family protein	NA	NA	NA	NA
WP_140875983.1\|5649245_5649590_-	DUF1768 domain-containing protein	A0A141ZK81	Faustovirus	2.8e-08	46.0
WP_140796562.1\|5649504_5649942_-	hypothetical protein	NA	NA	NA	NA
WP_140875985.1\|5650744_5655841_+	DUF4157 domain-containing protein	NA	NA	NA	NA
WP_140855660.1\|5655844_5656594_+	hypothetical protein	NA	NA	NA	NA
WP_140875987.1\|5656590_5657601_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_140793168.1\|5657752_5658346_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_140875989.1\|5658342_5659074_+	hypothetical protein	NA	NA	NA	NA
WP_140875991.1\|5659118_5661503_+\|tail	phage tail sheath subtilisin-like domain-containing protein	H6WFT7	Cyanophage	4.1e-18	34.6
WP_011554491.1\|5661521_5661977_+\|tail	phage tail protein	NA	NA	NA	NA
WP_140875993.1\|5662005_5663577_+\|tail	phage tail sheath protein	NA	NA	NA	NA

DBSCAN-SWA_9

6074777 : 6196351

105

Agrobacterium_phage(17.65%)

portal,tail,capsid,transposase,head,bacteriocin,protease,integrase,plate

attL 6153992:6154015|attR 6181658:6181681

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140793660.1\|6074777_6076145_+\|plate	type VI secretion system baseplate subunit TssK	NA	NA	NA	NA
WP_140793662.1\|6076160_6076877_+	DotU family type IV/VI secretion system protein	NA	NA	NA	NA
WP_140876229.1\|6076873_6080569_+	type VI secretion system membrane subunit TssM	NA	NA	NA	NA
WP_140799210.1\|6080570_6081503_+	type VI secretion system-associated protein TagF	NA	NA	NA	NA
WP_140876231.1\|6081518_6083576_+	type VI secretion system protein TssA	NA	NA	NA	NA
WP_011554793.1\|6083658_6084153_+	type VI secretion system contractile sheath small subunit	NA	NA	NA	NA
WP_140793670.1\|6084178_6085663_+	type VI secretion system contractile sheath large subunit	NA	NA	NA	NA
WP_140793671.1\|6085782_6086274_+	type VI secretion system tube protein Hcp	NA	NA	NA	NA
WP_011554796.1\|6086357_6086753_+\|plate	type VI secretion system baseplate subunit TssE	NA	NA	NA	NA
WP_140793672.1\|6086790_6088542_+\|plate	type VI secretion system baseplate subunit TssF	NA	NA	NA	NA
WP_174258882.1\|6088505_6089549_+\|plate	type VI secretion system baseplate subunit TssG	NA	NA	NA	NA
WP_140793674.1\|6089632_6092290_+	type VI secretion system ATPase TssH	A0A1S6UBG5	Serratia_phage	5.9e-98	35.3
WP_140876234.1\|6092298_6093393_+	hypothetical protein	NA	NA	NA	NA
WP_140793678.1\|6093542_6093908_+	HPF/RaiA family ribosome-associated protein	NA	NA	NA	NA
WP_140876236.1\|6093967_6094525_+	redoxin domain-containing protein	NA	NA	NA	NA
WP_140876238.1\|6094543_6095911_-	family 16 glycosylhydrolase	NA	NA	NA	NA
WP_140799220.1\|6096005_6097073_-	TOBE-like domain-containing protein	G3M9Y6	Bacillus_virus	2.7e-25	33.2
WP_140793686.1\|6097069_6097918_-	sulfate ABC transporter permease subunit CysW	NA	NA	NA	NA
WP_140793688.1\|6097923_6098766_-	sulfate ABC transporter permease subunit CysT	NA	NA	NA	NA
WP_140878435.1\|6098778_6099789_-	sulfate ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_140876240.1\|6100182_6103632_+	AAA family ATPase	A0A223W0B1	Agrobacterium_phage	1.1e-56	29.5
WP_140876242.1\|6103636_6107023_+	AAA family ATPase	A0A223W0B1	Agrobacterium_phage	6.2e-68	30.1
WP_140876244.1\|6107024_6109319_+	AAA family ATPase	A0A223W0B1	Agrobacterium_phage	1.2e-54	29.1
WP_140793696.1\|6109374_6109956_-	superoxide dismutase	Q56AR7	Bacillus_thuringiensis_phage	7.4e-46	46.8
WP_140876246.1\|6109981_6110482_-	flavin reductase	NA	NA	NA	NA
WP_140876248.1\|6110691_6111687_+	hypothetical protein	NA	NA	NA	NA
WP_140876250.1\|6111762_6114024_-	molybdopterin-dependent oxidoreductase	NA	NA	NA	NA
WP_140793704.1\|6114034_6114496_-	2Fe-2S iron-sulfur cluster binding domain-containing protein	NA	NA	NA	NA
WP_174259328.1\|6114492_6115146_-	Isoquinoline 1-oxidoreductase subunit	NA	NA	NA	NA
WP_140876252.1\|6115223_6117878_-	AAA family ATPase	K4FB40	Cronobacter_phage	3.8e-129	40.6
WP_140793710.1\|6118043_6118478_+	hypothetical protein	NA	NA	NA	NA
WP_140855927.1\|6118554_6119121_+	hypothetical protein	NA	NA	NA	NA
WP_140793714.1\|6119302_6120766_+	MFS transporter	NA	NA	NA	NA
WP_140799237.1\|6120792_6122271_-	glycoside hydrolase family 6 protein	NA	NA	NA	NA
WP_140799239.1\|6122425_6124099_-	amidase	NA	NA	NA	NA
WP_140799241.1\|6124153_6125260_-	saccharopine dehydrogenase NADP-binding domain-containing protein	NA	NA	NA	NA
WP_140800752.1\|6125359_6126244_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140799243.1\|6126284_6128270_+	RecQ family ATP-dependent DNA helicase	F2NZ48	Diadromus_pulchellus_ascovirus	4.3e-61	44.0
WP_140799245.1\|6128276_6129233_-	pirin family protein	NA	NA	NA	NA
WP_140793726.1\|6129498_6130713_-	protein kinase	NA	NA	NA	NA
WP_140876254.1\|6130805_6132596_-	protein kinase	A0A146JFA3	Tokyovirus	3.1e-10	27.2
WP_140793730.1\|6132592_6133456_-	DUF2381 family protein	NA	NA	NA	NA
WP_140793732.1\|6133647_6134223_-	hypothetical protein	NA	NA	NA	NA
WP_140793734.1\|6134226_6135555_-	AHH domain-containing protein	NA	NA	NA	NA
WP_140793736.1\|6136153_6136432_+	hypothetical protein	NA	NA	NA	NA
WP_140876256.1\|6137161_6137461_-	hypothetical protein	NA	NA	NA	NA
WP_140793738.1\|6137457_6137910_-	hypothetical protein	NA	NA	NA	NA
WP_140796578.1\|6137922_6138456_-	M15 family metallopeptidase	NA	NA	NA	NA
WP_140793740.1\|6138455_6138716_-	hypothetical protein	NA	NA	NA	NA
WP_140878437.1\|6139234_6139822_+\|bacteriocin	bacteriocin fulvocin C-related protein	NA	NA	NA	NA
WP_140793742.1\|6139931_6143168_-	hypothetical protein	NA	NA	NA	NA
WP_140793744.1\|6143174_6143936_-	hypothetical protein	NA	NA	NA	NA
WP_174259329.1\|6143937_6146316_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140876259.1\|6146410_6146806_-\|transposase	transposase	NA	NA	NA	NA
WP_140876261.1\|6146724_6147441_-\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
WP_140853493.1\|6147437_6147998_-\|transposase	transposase	NA	NA	NA	NA
WP_140793746.1\|6148244_6148598_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140793748.1\|6148630_6149293_-	hypothetical protein	NA	NA	NA	NA
WP_140876263.1\|6149292_6149718_-	hypothetical protein	NA	NA	NA	NA
WP_140876265.1\|6149726_6150143_-	hypothetical protein	NA	NA	NA	NA
WP_140876267.1\|6150179_6150599_-	hypothetical protein	NA	NA	NA	NA
WP_140793756.1\|6150598_6150922_-	hypothetical protein	NA	NA	NA	NA
WP_140876269.1\|6150921_6151578_-	hypothetical protein	NA	NA	NA	NA
WP_140799311.1\|6151668_6152082_-	hypothetical protein	NA	NA	NA	NA
WP_140876271.1\|6152093_6153182_-\|capsid	phage major capsid protein	NA	NA	NA	NA
WP_140876273.1\|6153178_6153988_-\|head,protease	HK97 family phage prohead protease	A0A142K631	Streptomyces_phage	1.5e-09	31.7
6153992:6154015	attL	NA	NA	NA	NA
WP_140876275.1\|6154023_6155352_-\|portal	phage portal protein	M1PLL1	Streptococcus_phage	7.4e-09	26.4
WP_140876277.1\|6155378_6156794_-	ATP/GTP-binding protein	A0A1V0DY66	Dinoroseobacter_phage	7.8e-57	37.0
WP_140876279.1\|6156786_6157263_-	hypothetical protein	NA	NA	NA	NA
WP_140878439.1\|6158968_6159673_-	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_140878441.1\|6160411_6162718_+	DNA primase	A0A2D1GN57	Marinobacter_phage	1.8e-66	38.1
WP_140876281.1\|6162751_6164065_+	PD-(D/E)XK nuclease family protein	NA	NA	NA	NA
WP_140876283.1\|6164068_6164833_-	hypothetical protein	NA	NA	NA	NA
WP_174259428.1\|6165273_6166779_+	helicase	NA	NA	NA	NA
WP_140876287.1\|6166826_6167249_-	TrmB family transcriptional regulator	NA	NA	NA	NA
WP_140876289.1\|6167831_6168362_+	hypothetical protein	NA	NA	NA	NA
WP_140876291.1\|6168445_6170455_+	DNA polymerase I	NA	NA	NA	NA
WP_174259330.1\|6170515_6170689_+	hypothetical protein	NA	NA	NA	NA
WP_140793792.1\|6170688_6171249_+	hypothetical protein	NA	NA	NA	NA
WP_140793794.1\|6171251_6171467_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_174259331.1\|6171463_6172684_+\|integrase	site-specific integrase	A4PE72	Ralstonia_virus	4.5e-21	30.8
WP_140876293.1\|6173007_6174222_-	protein kinase	NA	NA	NA	NA
WP_140876295.1\|6174314_6176105_-	protein kinase	A0A146JFA3	Tokyovirus	6.3e-11	28.6
WP_140876297.1\|6176101_6176965_-	DUF2381 family protein	NA	NA	NA	NA
WP_140876300.1\|6177156_6177726_-	hypothetical protein	NA	NA	NA	NA
WP_140878445.1\|6177729_6179052_-	AHH domain-containing protein	NA	NA	NA	NA
WP_140799299.1\|6179609_6179960_+	calmodulin	NA	NA	NA	NA
WP_140876302.1\|6180050_6180353_-	hypothetical protein	NA	NA	NA	NA
WP_140876304.1\|6180349_6180802_-	hypothetical protein	NA	NA	NA	NA
WP_140878447.1\|6180814_6181348_-	M15 family metallopeptidase	NA	NA	NA	NA
WP_140876307.1\|6181347_6181608_-	hypothetical protein	NA	NA	NA	NA
WP_140876309.1\|6181741_6182629_+	hypothetical protein	NA	NA	NA	NA
6181658:6181681	attR	NA	NA	NA	NA
WP_140876311.1\|6182648_6185885_-	hypothetical protein	NA	NA	NA	NA
WP_140876313.1\|6185891_6186653_-	hypothetical protein	NA	NA	NA	NA
WP_174259332.1\|6186654_6189033_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140793746.1\|6189254_6189608_-\|tail	phage tail protein	NA	NA	NA	NA
WP_140876315.1\|6189639_6190296_-	hypothetical protein	NA	NA	NA	NA
WP_140799307.1\|6190295_6190721_-	hypothetical protein	NA	NA	NA	NA
WP_140793820.1\|6190729_6191146_-	hypothetical protein	NA	NA	NA	NA
WP_140876317.1\|6191182_6191602_-	hypothetical protein	NA	NA	NA	NA
WP_140793756.1\|6191601_6191925_-	hypothetical protein	NA	NA	NA	NA
WP_140876319.1\|6191924_6192581_-	hypothetical protein	NA	NA	NA	NA
WP_140799311.1\|6192671_6193085_-	hypothetical protein	NA	NA	NA	NA
WP_140876321.1\|6194180_6194987_-\|head,protease	HK97 family phage prohead protease	A0A142K631	Streptomyces_phage	2.0e-09	31.7
WP_140876323.1\|6195022_6196351_-\|portal	phage portal protein	M1PLL1	Streptococcus_phage	5.7e-09	26.4

DBSCAN-SWA_10

6601243 : 6711504

Pseudomonas_phage(21.43%)

protease,transposase,tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140876529.1\|6601243_6602038_+\|transposase	transposase	S5VTD3	Leptospira_phage	8.9e-10	25.9
WP_140876531.1\|6602051_6602813_-	ATP-binding protein	NA	NA	NA	NA
WP_140876533.1\|6602809_6604312_-\|transposase	IS21 family transposase	A0A2L1IVA1	Escherichia_phage	4.9e-33	33.9
WP_140876535.1\|6604888_6605254_+	hypothetical protein	NA	NA	NA	NA
WP_140878465.1\|6605215_6606438_-\|transposase	IS3 family transposase	A0A1B0Z042	Pseudomonas_phage	1.9e-59	47.0
WP_174259150.1\|6606561_6607272_+\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	1.7e-36	39.7
WP_140878467.1\|6607317_6607584_+\|transposase	IS66 family transposase zinc-finger binding domain-containing protein	NA	NA	NA	NA
WP_140878469.1\|6608483_6611828_-	RHS repeat-associated core domain-containing protein	NA	NA	NA	NA
WP_140878471.1\|6615341_6616748_-	dNTP triphosphohydrolase	NA	NA	NA	NA
WP_140876539.1\|6616994_6617510_+	OmpA family protein	NA	NA	NA	NA
WP_140876541.1\|6617512_6619135_-	GMC family oxidoreductase N-terminal domain-containing protein	NA	NA	NA	NA
WP_140876543.1\|6619415_6620636_+	M20/M25/M40 family metallo-hydrolase	NA	NA	NA	NA
WP_140794293.1\|6620740_6622498_+	ATP-binding cassette domain-containing protein	W8CYL7	Bacillus_phage	1.6e-64	30.5
WP_140876545.1\|6622502_6624926_-	ABC transporter permease	NA	NA	NA	NA
WP_140794295.1\|6625159_6625402_+	hypothetical protein	NA	NA	NA	NA
WP_140796604.1\|6625735_6625981_+	hypothetical protein	NA	NA	NA	NA
WP_140856213.1\|6626055_6627033_+	glycosyltransferase family 9 protein	NA	NA	NA	NA
WP_140876547.1\|6627064_6628570_-	radical SAM protein	S5VT21	Leptospira_phage	1.2e-36	26.5
WP_140876549.1\|6628566_6629988_-	HEXXH motif domain-containing protein	NA	NA	NA	NA
WP_140876551.1\|6629987_6631685_-	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_140799459.1\|6631766_6633854_-	hypothetical protein	NA	NA	NA	NA
WP_140876552.1\|6634275_6636825_-	protein kinase	S4VV57	Pandoravirus	3.2e-24	36.0
WP_140794303.1\|6636906_6637107_-	hypothetical protein	NA	NA	NA	NA
WP_140794304.1\|6637242_6638013_-	exodeoxyribonuclease III	NA	NA	NA	NA
WP_140876554.1\|6638210_6639311_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_140794307.1\|6639535_6642034_+	PBP1A family penicillin-binding protein	NA	NA	NA	NA
WP_140856225.1\|6642030_6643389_+	VCBS repeat-containing protein	NA	NA	NA	NA
WP_140876556.1\|6643385_6644756_+	peptide ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_140794310.1\|6644766_6646416_+	HAMP domain-containing protein	NA	NA	NA	NA
WP_140876558.1\|6646417_6647242_-	class I SAM-dependent methyltransferase	NA	NA	NA	NA
WP_140794312.1\|6647308_6647641_-	QacE family quaternary ammonium compound efflux SMR transporter	NA	NA	NA	NA
WP_140876560.1\|6647778_6649872_-	cell division protein FtsK	NA	NA	NA	NA
WP_090491726.1\|6650016_6650376_-	ribosome-associated translation inhibitor RaiA	NA	NA	NA	NA
WP_163884322.1\|6650545_6650908_+	response regulator	NA	NA	NA	NA
WP_140794314.1\|6650991_6651474_+	DUF2007 domain-containing protein	NA	NA	NA	NA
WP_140876562.1\|6651480_6652446_-	DUF1460 domain-containing protein	NA	NA	NA	NA
WP_140876564.1\|6652442_6653498_-	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_011555164.1\|6653575_6653893_+	DUF4398 domain-containing protein	NA	NA	NA	NA
WP_174258902.1\|6653910_6655320_+	OmpA family protein	NA	NA	NA	NA
WP_140876566.1\|6655412_6656447_-\|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
WP_140799469.1\|6656443_6657781_-	DUF4388 domain-containing protein	NA	NA	NA	NA
WP_140794320.1\|6657788_6658781_-	thioredoxin domain-containing protein	NA	NA	NA	NA
WP_140856236.1\|6658853_6659915_+	type I asparaginase	NA	NA	NA	NA
WP_026114337.1\|6659975_6660887_+	GGDEF domain-containing protein	A0A127AWB9	Bacillus_phage	4.0e-22	35.5
WP_140856238.1\|6660914_6662528_-	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_002614080.1\|6662639_6662834_+	30S ribosomal protein S21	NA	NA	NA	NA
WP_174259341.1\|6662938_6663397_+	GatB/YqeY domain-containing protein	A0A292GL36	Xanthomonas_phage	5.0e-13	35.8
WP_174258903.1\|6663729_6665550_+	DNA primase	A0A1S5RF71	Helicobacter_phage	8.5e-40	32.3
WP_140794325.1\|6665642_6667769_+	RNA polymerase sigma factor RpoD	A0A2I7SAT0	Vibrio_phage	2.5e-35	36.7
WP_140856244.1\|6667793_6668237_+	MGMT family protein	NA	NA	NA	NA
WP_140876568.1\|6668605_6669124_+	hypothetical protein	NA	NA	NA	NA
WP_140794328.1\|6669008_6670664_+	hypothetical protein	NA	NA	NA	NA
WP_161604917.1\|6670724_6671036_+\|transposase	transposase	NA	NA	NA	NA
WP_140876570.1\|6671131_6672350_+\|transposase	IS3 family transposase	A0A1B0Z042	Pseudomonas_phage	1.1e-59	47.3
WP_140876572.1\|6672386_6672758_+	GFA family protein	NA	NA	NA	NA
WP_140794332.1\|6672889_6673810_-	hypothetical protein	NA	NA	NA	NA
WP_140794333.1\|6674623_6675193_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_140799472.1\|6675248_6676196_+	cation diffusion facilitator family transporter	NA	NA	NA	NA
WP_140876574.1\|6676414_6676834_-	MAPEG family protein	NA	NA	NA	NA
WP_140876576.1\|6677267_6677921_+	hypothetical protein	NA	NA	NA	NA
WP_140876578.1\|6677877_6679341_-	aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme	NA	NA	NA	NA
WP_174259151.1\|6680216_6680447_-	hypothetical protein	NA	NA	NA	NA
WP_140875896.1\|6682209_6683034_+\|transposase	IS3 family transposase	A0A1B0Z042	Pseudomonas_phage	1.6e-57	46.9
WP_140876582.1\|6683238_6683697_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_161607126.1\|6683960_6684311_+\|transposase	transposase	NA	NA	NA	NA
WP_140878473.1\|6684808_6687361_+	DUF1929 domain-containing protein	NA	NA	NA	NA
WP_140876586.1\|6687517_6688906_-\|protease	protease B	NA	NA	NA	NA
WP_140876588.1\|6689537_6690518_+	hypothetical protein	NA	NA	NA	NA
WP_140876590.1\|6691421_6692126_-	hypothetical protein	NA	NA	NA	NA
WP_140876592.1\|6693143_6693758_-	hypothetical protein	NA	NA	NA	NA
WP_140876594.1\|6693843_6695346_-	glycosyltransferase family 39 protein	NA	NA	NA	NA
WP_161607127.1\|6695689_6695953_-\|transposase	transposase	NA	NA	NA	NA
WP_140876596.1\|6696409_6697843_-	hypothetical protein	NA	NA	NA	NA
WP_140876598.1\|6698347_6699175_+	hypothetical protein	NA	NA	NA	NA
WP_161607128.1\|6699599_6699773_+	hypothetical protein	NA	NA	NA	NA
WP_140799484.1\|6699823_6701146_-	leucine-rich repeat domain-containing protein	NA	NA	NA	NA
WP_140876600.1\|6701236_6702667_-	GTPase HflX	NA	NA	NA	NA
WP_140876602.1\|6702836_6704108_+	DEAD/DEAH box helicase	A0A0N9Q9J4	Chrysochromulina_ericina_virus	6.1e-45	32.0
WP_140876604.1\|6704257_6705157_+	RluA family pseudouridine synthase	NA	NA	NA	NA
WP_140794353.1\|6705344_6705695_-	hypothetical protein	NA	NA	NA	NA
WP_161604920.1\|6706048_6707659_+	VCBS repeat-containing protein	NA	NA	NA	NA
WP_140873086.1\|6710181_6711504_-\|transposase	transposase	NA	NA	NA	NA

DBSCAN-SWA_11

7766134 : 7861265

Paramecium_bursaria_Chlorella_virus(33.33%)

transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_162520988.1\|7766134_7766446_+\|transposase	transposase	NA	NA	NA	NA
WP_174259365.1\|7766494_7767847_+	hypothetical protein	NA	NA	NA	NA
WP_140877169.1\|7768332_7771635_-	hypothetical protein	NA	NA	NA	NA
WP_140877171.1\|7773047_7774313_+	DUF1214 domain-containing protein	M1HNU9	Paramecium_bursaria_Chlorella_virus	4.7e-53	32.4
WP_140877173.1\|7774678_7774864_+	prolyl oligopeptidase family serine peptidase	NA	NA	NA	NA
WP_140877175.1\|7775026_7776985_-	phosphoesterase	NA	NA	NA	NA
WP_140796666.1\|7777682_7778426_+	UTRA domain-containing protein	NA	NA	NA	NA
WP_140795105.1\|7778441_7779308_+	TSUP family transporter	NA	NA	NA	NA
WP_140795106.1\|7779304_7779622_+	DUF1634 domain-containing protein	NA	NA	NA	NA
WP_140877177.1\|7780172_7781180_+	hypothetical protein	NA	NA	NA	NA
WP_140796667.1\|7781454_7782792_+	hypothetical protein	NA	NA	NA	NA
WP_140877179.1\|7782828_7784145_+	DUF1214 domain-containing protein	M1I2Z8	Paramecium_bursaria_Chlorella_virus	7.5e-54	33.0
WP_140878532.1\|7784410_7785046_+\|transposase	transposase	NA	NA	NA	NA
WP_140799864.1\|7785425_7786292_+	hypothetical protein	NA	NA	NA	NA
WP_140877181.1\|7786557_7788471_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_161607135.1\|7788808_7789594_+	anti-sigma factor antagonist	NA	NA	NA	NA
WP_140877185.1\|7791634_7793389_-	DUF5050 domain-containing protein	NA	NA	NA	NA
WP_161607136.1\|7793624_7794122_+\|transposase	transposase	NA	NA	NA	NA
WP_161607137.1\|7794616_7794847_-	hypothetical protein	NA	NA	NA	NA
WP_140877191.1\|7795066_7795972_+	hypothetical protein	NA	NA	NA	NA
WP_140795115.1\|7796547_7797564_-	alcohol dehydrogenase catalytic domain-containing protein	M1PHA2	Moumouvirus	1.0e-26	26.0
WP_140877193.1\|7797936_7798833_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_140795117.1\|7799472_7800354_+	EamA family transporter	NA	NA	NA	NA
WP_140877194.1\|7800827_7803851_-	efflux RND transporter permease subunit	S5VTK5	Leptospira_phage	1.5e-78	24.2
WP_161604928.1\|7803847_7804792_-	efflux RND transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_161607138.1\|7804910_7806107_-	TolC family protein	NA	NA	NA	NA
WP_140795121.1\|7806311_7807358_+	hypothetical protein	NA	NA	NA	NA
WP_140877198.1\|7807540_7808572_+	peptidylprolyl isomerase	NA	NA	NA	NA
WP_140795123.1\|7808597_7808999_-	hypothetical protein	NA	NA	NA	NA
WP_140877200.1\|7809116_7809458_-	PhnA domain-containing protein	NA	NA	NA	NA
WP_140877202.1\|7809856_7814404_-	aldo/keto reductase	NA	NA	NA	NA
WP_161607139.1\|7814447_7817051_-	Ig-like domain-containing protein	NA	NA	NA	NA
WP_140878534.1\|7817210_7820630_-	hypothetical protein	NA	NA	NA	NA
WP_011556093.1\|7820746_7821403_-	response regulator transcription factor	NA	NA	NA	NA
WP_140796670.1\|7821380_7824512_-	histidine kinase	NA	NA	NA	NA
WP_140795127.1\|7825006_7825351_-\|transposase	transposase	NA	NA	NA	NA
WP_140795129.1\|7825495_7825921_-	hypothetical protein	NA	NA	NA	NA
WP_140799878.1\|7826751_7827501_+	NmrA family NAD(P)-binding protein	NA	NA	NA	NA
WP_140795131.1\|7827515_7828016_+	Ohr family peroxiredoxin	NA	NA	NA	NA
WP_140796671.1\|7828117_7828522_+	cupin domain-containing protein	NA	NA	NA	NA
WP_140800804.1\|7829640_7830180_-	hypothetical protein	NA	NA	NA	NA
WP_140795133.1\|7831165_7832578_+	aminotransferase class V-fold PLP-dependent enzyme	NA	NA	NA	NA
WP_140857010.1\|7832819_7833119_-	hypothetical protein	NA	NA	NA	NA
WP_140858568.1\|7833588_7834584_+	PQQ-binding-like beta-propeller repeat protein	NA	NA	NA	NA
WP_140877208.1\|7835244_7837392_-	hypothetical protein	NA	NA	NA	NA
WP_140877210.1\|7837517_7839545_+	lipoxygenase	NA	NA	NA	NA
WP_140857014.1\|7839565_7841002_+	cytochrome P450	NA	NA	NA	NA
WP_140799884.1\|7840998_7841844_+	fatty acid desaturase	NA	NA	NA	NA
WP_140795140.1\|7842931_7844290_+	peptidoglycan DD-metalloendopeptidase family protein	A0A1P8VV77	Rathayibacter_phage	3.2e-15	38.3
WP_140878536.1\|7845102_7846782_+	hypothetical protein	NA	NA	NA	NA
WP_161605187.1\|7847143_7848598_-	S8 family serine peptidase	NA	NA	NA	NA
WP_140877212.1\|7849037_7849802_+	hypothetical protein	NA	NA	NA	NA
WP_140795143.1\|7849979_7851407_+	hypothetical protein	NA	NA	NA	NA
WP_140857022.1\|7852420_7854178_-	DUF5050 domain-containing protein	NA	NA	NA	NA
WP_174258949.1\|7854353_7854518_-	hypothetical protein	NA	NA	NA	NA
WP_140877214.1\|7854785_7857206_+	tandem-95 repeat protein	NA	NA	NA	NA
WP_140877216.1\|7857354_7859712_-	hypothetical protein	NA	NA	NA	NA
WP_140877218.1\|7859712_7860642_-\|transposase	transposase	A0A218MNE7	uncultured_virus	2.2e-23	34.0
WP_140877220.1\|7860767_7861265_-\|transposase	IS66 family transposase zinc-finger binding domain-containing protein	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr_ID: NZ_CP017172.1|WP_140875278.1|4323033_4323219_+|hypothetical-protein

Click the colored protein region to show detailed information

Acr ID

Acr position

Acr size

Homology with known anti

Neighbor HTH/AcRanker

Neighbor Aca

In prophage

Protospacer in prophage

NZ_CP017172.1|WP_140875278.1|4323033_4323219_+|hypothetical-protein

4323033_4323219_+

61 aa aa

4303180-4324484

yes

CRISPR ID	CRISPR type	Spacer info	Spacer location	Spacer length	Protospacer location	Mismatch
NZ_CP017172_19	TypeI	19.30\|8875568\|35\|NZ_CP017172\|CRISPRCasFinder,CRT,PILER-CR	8875568-8875602	35	4324267-4324233	1

1. spacer 19.30|8875568|35|NZ_CP017172|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017172 position: 4324267-4324233, mismatch: 1

cggatgccgtccaagtcacaccgggccgcgagcgc	CRISPR spacer
cggatgccgtccaagtcacaccgcgccgcgagcgc	Protospacer
*********************** ***********

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP017172

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

Click the colored protein region to show detailed information