ID   CSM2_MYCTU              Reviewed;         124 AA.
AC   P9WJG1; F2GLB2; L0TDN3; P71630; Q7D6I2;
DT   16-APR-2014, integrated into UniProtKB/Swiss-Prot.
DT   16-APR-2014, sequence version 1.
DT   25-MAY-2022, entry version 33.
DE   RecName: Full=CRISPR system Cms protein Csm2;
DE   AltName: Full=CRISPR type III A-associated protein Csm2;
GN   Name=csm2; OrderedLocusNames=Rv2822c;
OS   Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv).
OC   Bacteria; Actinobacteria; Corynebacteriales; Mycobacteriaceae;
OC   Mycobacterium; Mycobacterium tuberculosis complex.
OX   NCBI_TaxID=83332;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=ATCC 25618 / H37Rv;
RX   PubMed=9634230; DOI=10.1038/31159;
RA   Cole S.T., Brosch R., Parkhill J., Garnier T., Churcher C.M., Harris D.E.,
RA   Gordon S.V., Eiglmeier K., Gas S., Barry C.E. III, Tekaia F., Badcock K.,
RA   Basham D., Brown D., Chillingworth T., Connor R., Davies R.M., Devlin K.,
RA   Feltwell T., Gentles S., Hamlin N., Holroyd S., Hornsby T., Jagels K.,
RA   Krogh A., McLean J., Moule S., Murphy L.D., Oliver S., Osborne J.,
RA   Quail M.A., Rajandream M.A., Rogers J., Rutter S., Seeger K., Skelton S.,
RA   Squares S., Squares R., Sulston J.E., Taylor K., Whitehead S.,
RA   Barrell B.G.;
RT   "Deciphering the biology of Mycobacterium tuberculosis from the complete
RT   genome sequence.";
RL   Nature 393:537-544(1998).
RN   [2]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   STRAIN=ATCC 25618 / H37Rv;
RX   PubMed=21969609; DOI=10.1074/mcp.m111.011627;
RA   Kelkar D.S., Kumar D., Kumar P., Balakrishnan L., Muthusamy B., Yadav A.K.,
RA   Shrivastava P., Marimuthu A., Anand S., Sundaram H., Kingsbury R.,
RA   Harsha H.C., Nair B., Prasad T.S., Chauhan D.S., Katoch K., Katoch V.M.,
RA   Kumar P., Chaerkady R., Ramachandran S., Dash D., Pandey A.;
RT   "Proteogenomic analysis of Mycobacterium tuberculosis by high resolution
RT   mass spectrometry.";
RL   Mol. Cell. Proteomics 10:M111.011627-M111.011627(2011).
RN   [3]
RP   FUNCTION IN PLASMID RESISTANCE, SUBUNIT, AND DISRUPTION PHENOTYPE.
RC   STRAIN=H37Rv;
RX   PubMed=29979631; DOI=10.1096/fj.201800557rr;
RA   Wei W., Zhang S., Fleming J., Chen Y., Li Z., Fan S., Liu Y., Wang W.,
RA   Wang T., Liu Y., Ren B., Wang M., Jiao J., Chen Y., Zhou Y., Zhou Y.,
RA   Gu S., Zhang X., Wan L., Chen T., Zhou L., Chen Y., Zhang X.E., Li C.,
RA   Zhang H., Bi L.;
RT   "Mycobacterium tuberculosis type III-A CRISPR/Cas system crRNA and its
RT   maturation have atypical features.";
RL   FASEB J. 33:1496-1509(2019).
CC   -!- FUNCTION: CRISPR (clustered regularly interspaced short palindromic
CC       repeat) is an adaptive immune system that provides protection against
CC       mobile genetic elements (viruses, transposable elements and conjugative
CC       plasmids). CRISPR clusters contain spacers, sequences complementary to
CC       antecedent mobile elements, and target invading nucleic acids. CRISPR
CC       clusters are transcribed and processed into CRISPR RNA (crRNA). The
CC       type III-A Csm effector complex binds crRNA and acts as a crRNA-guided
CC       RNase, DNase and cyclic oligoadenylate synthase; binding of target RNA
CC       cognate to the crRNA is required for all activities (Probable). This
CC       CRISPR-Cas system protects bacteria against transformation with
CC       plasmids containing DNA homologous to its spacer regions
CC       (PubMed:29979631). {ECO:0000269|PubMed:29979631,
CC       ECO:0000305|PubMed:29979631}.
CC   -!- FUNCTION: This subunit may be involved in monitoring complementarity of
CC       crRNA and target RNA. {ECO:0000250|UniProtKB:A0A0A7HIX1}.
CC   -!- SUBUNIT: Part of the Csm effector complex that includes Cas10, Csm2,
CC       Csm3, Csm4 and Csm5. {ECO:0000269|PubMed:29979631}.
CC   -!- DISRUPTION PHENOTYPE: Deletion of the entire CRISPR-Cas locus (cas6 to
CC       cas2, Rv2824c to Rv2816c) decreases resistance to plasmids encoding
CC       spacer elements about 6-fold. {ECO:0000269|PubMed:29979631}.
CC   -!- MISCELLANEOUS: Encoded in a type III-A CRISPR locus.
CC       {ECO:0000305|PubMed:29979631}.
CC   -!- SIMILARITY: Belongs to the CRISPR-associated Csm2 family.
CC       {ECO:0000305}.
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DR   EMBL; AL123456; CCP45622.1; -; Genomic_DNA.
DR   PIR; A70692; A70692.
DR   RefSeq; NP_217338.1; NC_000962.3.
DR   RefSeq; WP_003414296.1; NZ_NVQJ01000006.1.
DR   AlphaFoldDB; P9WJG1; -.
DR   SMR; P9WJG1; -.
DR   STRING; 83332.Rv2822c; -.
DR   PaxDb; P9WJG1; -.
DR   DNASU; 887778; -.
DR   GeneID; 887778; -.
DR   KEGG; mtu:Rv2822c; -.
DR   TubercuList; Rv2822c; -.
DR   eggNOG; COG1421; Bacteria.
DR   OMA; YCKYFEA; -.
DR   Proteomes; UP000001584; Chromosome.
DR   GO; GO:0003723; F:RNA binding; IEA:UniProtKB-KW.
DR   GO; GO:0051607; P:defense response to virus; IEA:UniProtKB-KW.
DR   CDD; cd09647; Csm2_III-A; 1.
DR   InterPro; IPR010149; CRISPR-assoc_prot_Csm2_III-A.
DR   Pfam; PF03750; Csm2_III-A; 1.
DR   TIGRFAMs; TIGR01870; cas_TM1810_Csm2; 1.
PE   1: Evidence at protein level;
KW   Antiviral defense; Reference proteome; RNA-binding.
FT   CHAIN           1..124
FT                   /note="CRISPR system Cms protein Csm2"
FT                   /id="PRO_0000418225"
SQ   SEQUENCE   124 AA;  14287 MW;  84B303DD7A1549AA CRC64;
     MSVIQDDYVK QAEVIRGLPK KKNGFELTTT QLRVLLSLTA QLFDEAQQSA NPTLPRQLKE
     KVQYLRVRFV YQSGREDAVK TFVRNAKLLE ALEGIGDSRD GLLRFCRYME ALAAYKKYLD
     PKDK