Mott Helen R, Owen Darerca
Department of Biochemistry, University of Cambridge , Cambridge , UK.
Crit Rev Biochem Mol Biol. 2015 Mar-Apr;50(2):85-133. doi: 10.3109/10409238.2014.999191. Epub 2015 Apr 1.
The Ras superfamily small G proteins are master regulators of a diverse range of cellular processes and act via downstream effector molecules. The first structure of a small G protein-effector complex, that of Rap1A with c-Raf1, was published 20 years ago. Since then, the structures of more than 60 small G proteins in complex with their effectors have been published. These effectors utilize a diverse array of structural motifs to interact with the G protein fold, which we have divided into four structural classes: intermolecular β-sheets, helical pairs, other interactions, and pleckstrin homology (PH) domains. These classes and their representative structures are discussed and a contact analysis of the interactions is presented, which highlights the common effector-binding regions between and within the small G protein families.
Ras超家族小G蛋白是多种细胞过程的主要调节因子,并通过下游效应分子发挥作用。小G蛋白-效应分子复合物的首个结构,即Rap1A与c-Raf1的复合物结构,于20年前发表。从那时起,已发表了60多种与效应分子形成复合物的小G蛋白的结构。这些效应分子利用多种结构基序与G蛋白折叠相互作用,我们将其分为四个结构类别:分子间β折叠片、螺旋对、其他相互作用和普列克底物蛋白同源(PH)结构域。本文讨论了这些类别及其代表性结构,并对相互作用进行了接触分析,突出了小G蛋白家族之间及内部的共同效应分子结合区域。