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The RHO Family GTPases: Mechanisms of Regulation and Signaling.
- Source :
-
Cells [Cells] 2021 Jul 20; Vol. 10 (7). Date of Electronic Publication: 2021 Jul 20. - Publication Year :
- 2021
-
Abstract
- Much progress has been made toward deciphering RHO GTPase functions, and many studies have convincingly demonstrated that altered signal transduction through RHO GTPases is a recurring theme in the progression of human malignancies. It seems that 20 canonical RHO GTPases are likely regulated by three GDIs, 85 GEFs, and 66 GAPs, and eventually interact with >70 downstream effectors. A recurring theme is the challenge in understanding the molecular determinants of the specificity of these four classes of interacting proteins that, irrespective of their functions, bind to common sites on the surface of RHO GTPases. Identified and structurally verified hotspots as functional determinants specific to RHO GTPase regulation by GDIs, GEFs, and GAPs as well as signaling through effectors are presented, and challenges and future perspectives are discussed.
- Subjects :
- Cardiovascular Diseases genetics
Cardiovascular Diseases metabolism
Cardiovascular Diseases pathology
Cognition Disorders genetics
Cognition Disorders metabolism
Cognition Disorders pathology
Communicable Diseases genetics
Communicable Diseases metabolism
Communicable Diseases pathology
GTPase-Activating Proteins metabolism
Gene Expression Regulation
Humans
Multigene Family
Neoplasms genetics
Neoplasms metabolism
Neoplasms pathology
Protein Isoforms genetics
Protein Isoforms metabolism
Rho Guanine Nucleotide Exchange Factors metabolism
Signal Transduction
cdc42 GTP-Binding Protein metabolism
rac1 GTP-Binding Protein metabolism
rho Guanine Nucleotide Dissociation Inhibitor alpha metabolism
rhoA GTP-Binding Protein metabolism
GTPase-Activating Proteins genetics
Rho Guanine Nucleotide Exchange Factors genetics
cdc42 GTP-Binding Protein genetics
rac1 GTP-Binding Protein genetics
rho Guanine Nucleotide Dissociation Inhibitor alpha genetics
rhoA GTP-Binding Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 10
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 34359999
- Full Text :
- https://doi.org/10.3390/cells10071831