RGS1

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

Regulator of G-protein signaling 1 is a protein that in humans is encoded by the RGS1 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesRGS1, 1R20, BL34, HEL-S-87, IER1, IR20, regulator of G-protein signaling 1, regulator of G protein signaling 1
Quick facts Available structures, PDB ...
RGS1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRGS1, 1R20, BL34, HEL-S-87, IER1, IR20, regulator of G-protein signaling 1, regulator of G protein signaling 1
External IDsOMIM: 600323; MGI: 1354694; HomoloGene: 2191; GeneCards: RGS1; OMA:RGS1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002922

NM_015811

RefSeq (protein)

NP_002913

NP_056626

Location (UCSC)Chr 1: 192.58 – 192.58 MbChr 1: 144.12 – 144.12 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a member of the regulator of G-protein signaling family. This protein is located on the cytosolic side of the plasma membrane and contains a conserved, 120 amino acid motif called the RGS domain. The protein attenuates the signalling activity of G-proteins by binding to activated, GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal.[7]

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