Structures of Ras superfamily effector complexes: What have we learnt in two decades?

Helen R Mott, Darerca Owen

Journal: Critical reviews in biochemistry and molecular biology 2016;50(2):85-133

PMID: 25830673

Abstract

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.

Address: Department of Biochemistry, University of Cambridge , Cambridge , UK.

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