SNRPB

Small nuclear ribonucleoprotein polypeptides B and B1

PDB rendering based on 1d3b.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols SNRPB ; CCMS; COD; SNRPB1; Sm-B/B'; SmB/B'; SmB/SmB'; snRNP-B
External IDs OMIM: 182282 MGI: 98342 HomoloGene: 134543 GeneCards: SNRPB Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 6628 20638
Ensembl ENSG00000125835 ENSMUSG00000027404
UniProt P14678 P27048
RefSeq (mRNA) NM_003091 NM_009225
RefSeq (protein) NP_003082 NP_033251
Location (UCSC) Chr 20:
2.46 – 2.47 Mb
Chr 2:
130.17 – 130.18 Mb
PubMed search

Small nuclear ribonucleoprotein-associated proteins B and B' is a protein that in humans is encoded by the SNRPB gene.[1][2]

Function

The protein encoded by this gene is one of several nuclear proteins that are found in common among U1, U2, U4/U6, and U5 small ribonucleoprotein particles (snRNPs). These snRNPs are involved in pre-mRNA splicing, and the encoded protein may also play a role in pre-mRNA splicing or snRNP structure. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding different isoforms (B and B') have been found for this gene.[2]

Interactions

SNRPB has been shown to interact with DDX20[3] and Coilin.[4]

References

  1. Griffith AJ, Schmauss C, Craft J (July 1992). "The murine gene encoding the highly conserved Sm B protein contains a nonfunctional alternative 3' splice site". Gene 114 (2): 195–201. doi:10.1016/0378-1119(92)90574-9. PMID 1376292.
  2. 1 2 "Entrez Gene: SNRPB small nuclear ribonucleoprotein polypeptides B and B1".
  3. Charroux B, Pellizzoni L, Perkinson RA, Shevchenko A, Mann M, Dreyfuss G (Dec 1999). "Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems". J. Cell Biol. 147 (6): 1181–94. doi:10.1083/jcb.147.6.1181. PMC 2168095. PMID 10601333.
  4. Hebert MD, Szymczyk PW, Shpargel KB, Matera AG (October 2001). "Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein". Genes Dev. 15 (20): 2720–9. doi:10.1101/gad.908401. PMC 312817. PMID 11641277.

Further reading


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