Published January 1, 2016
| Version v1
Journal article
Open
Ras Conformational Ensembles, Allostery, and Signaling
Creators
- 1. NCI, Canc & Inflammat Program, Leidos Biomed Res Inc, Frederick Natl Lab, Frederick, MD 21702 USA
- 2. Koc Univ, Dept Chem & Biol Engn, Rumelifeneri Yolu, TR-34450 Sariyer, Turkey
- 3. Koc Univ, Dept Comp Engn, Rumelifeneri Yolu, TR-34450 Sariyer, Turkey
- 4. Shanghai Jiao Tong Univ, Sch Med, Dept Pathophysiol,Chinese Minist Educ, Shanghai Univ E Inst Chem Biol,Key Lab Cell Diffe, Shanghai 200025, Peoples R China
Description
Ras proteins are classical members of small GTPases that function as molecular switches by alternating between inactive GDP-bound and active GTP-bound states. Ras activation is regulated by guanine nucleotide exchange factors that catalyze the exchange of GDP by GTP, and inactivation is terminated by GTPase-activating proteins that accelerate the intrinsic GTP hydrolysis rate by orders of magnitude. In this review, we focus on data that have accumulated over the past few years pertaining to the conformational ensembles and the allosteric regulation of Ras proteins and their interpretation from our conformational landscape standpoint. The Ras ensemble embodies all states, including the ligand-bound conformations, the activated (or inactivated) allosteric modulated states, post-translationally modified states, mutational states, transition states, and nonfunctional states serving as a reservoir for emerging functions. The ensemble is shifted by distinct mutational events, cofactors, post-translational modifications, and different membrane compositions. A better understanding of Ras biology can contribute to therapeutic strategies.
Files
bib-24931ea8-13fa-4637-8678-de943ce35593.txt
Files
(185 Bytes)
| Name | Size | Download all |
|---|---|---|
|
md5:0366091b945d72c5769077d97d2bbc04
|
185 Bytes | Preview Download |