RASA3

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

Ras GTPase-activating protein 3 is an enzyme that in humans is encoded by the RASA3 gene.[5][6][7]

AliasesRASA3, GAP1IP4BP, GAPIII, RAS p21 protein activator 3
End114,132,623 bp[1]
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RASA3
Identifiers
AliasesRASA3, GAP1IP4BP, GAPIII, RAS p21 protein activator 3
External IDsOMIM: 605182; MGI: 1197013; HomoloGene: 7217; GeneCards: RASA3; OMA:RASA3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007368
NM_001320821
NM_001320822

NM_009025

RefSeq (protein)

NP_001307750
NP_001307751
NP_031394

NP_033051

Location (UCSC)Chr 13: 113.98 – 114.13 MbChr 8: 13.62 – 13.73 Mb
PubMed search[3][4]
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The protein encoded by this gene is member of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. This family member is an inositol 1,3,4,5-tetrakisphosphate-binding protein, like the closely related RAS p21 protein activator 2. The two family members have distinct pleckstrin-homology domains, with this particular member having a domain consistent with its localization to the plasma membrane.[7] It has been shown that RASA3 promotes a shift from noncanonical to canonical TGF-β signaling through SMAD3 in B cells.[8]

Interactions

RASA3 has been shown to interact with HCK.[9]

References

Further reading

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