RGS10

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Regulator of G-protein signaling 10 is a protein that in humans is encoded by the RGS10 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesRGS10, regulator of G protein signaling 10
Quick facts Available structures, PDB ...
RGS10
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRGS10, regulator of G protein signaling 10
External IDsOMIM: 602856; MGI: 1915115; HomoloGene: 37710; GeneCards: RGS10; OMA:RGS10 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002925
NM_001005339

NM_026418

RefSeq (protein)

NP_001005339
NP_002916

NP_080694

Location (UCSC)Chr 10: 119.5 – 119.54 MbChr 7: 127.98 – 128.02 Mb
PubMed search[3][4]
Wikidata
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Function

Regulator of G protein signaling (RGS) family members are regulatory molecules that act as GTPase activating proteins (GAPs) for G alpha subunits of heterotrimeric G proteins. RGS proteins are able to deactivate G protein subunits of the Gi alpha, Go alpha and Gq alpha subtypes. They drive G proteins into their inactive GDP-bound forms. Regulator of G protein signaling 10 belongs to this family. All RGS proteins share a conserved 120-amino acid sequence termed the RGS domain. This protein associates specifically with the activated forms of the two related G-protein subunits, G-alphai3 and G-alphaz but fails to interact with the structurally and functionally distinct G-alpha subunits. Regulator of G protein signaling 10 protein is localized in the nucleus. Two transcript variants encoding different isoforms have been found for this gene.[6]

Interactions

RGS10 has been shown to interact with SAP18[7] and GNAI3.[5]

References

Further reading

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