RAC3

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Ras-related C3 botulinum toxin substrate 3 (Rac3) is a G protein that in humans is encoded by the RAC3 gene.[5] It is an important component of intracellular signalling pathways. Rac3 is a member of the Rac subfamily of the Rho family of small G proteins.[6][7] Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases.[5]

PDBOrtholog search: PDBe RCSB
AliasesRAC3, ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3), Rac family small GTPase 3
Quick facts Available structures, PDB ...
RAC3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRAC3, ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3), Rac family small GTPase 3
External IDsOMIM: 602050; MGI: 2180784; HomoloGene: 68433; GeneCards: RAC3; OMA:RAC3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005052
NM_001316307

NM_133223

RefSeq (protein)

NP_001303236
NP_005043

NP_573486

Location (UCSC)Chr 17: 82.03 – 82.03 MbChr 11: 120.61 – 120.61 Mb
PubMed search[3][4]
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Interactions

RAC3 has been shown to interact with CIB1[8] and HNF1A.[9] RAC3 also interacts with Nrf2 proteins.[10] ETAR, ILK, and β-arr1 interact with RAC3 as well.[11]

Location

RAC3 gene is located in the third sub-band of the fifth band in the second region of the q arm on chromosome 17. There's many tumor suppressor genes that are located around the RAC3 gene.[12]

Therapeutic use

Since the RAC3 gene is over-expressed in carcinoma cells, it can function as a therapeutic target for the treatment of different cancer such as lung adenocarcinoma. To become invasive, epithelial cells have to transform into mesenchymal cells and the transformation is regulated by the RAC3 gene. As a result, if the RAC3 gene is silenced, lung adenocarcinoma cells cannot metastasize. In addition, drugs designed to silence the RAC3 gene lead to the apoptosis of tumor cells, thus preventing the cells from colonizing.[13]

Pathological mutations

Mutations of the RAC3 gene may result in neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, first described in 2018 by White et al.

References

Further reading

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