WD40 domain

G beta protein is in red. It contains a seven-bladed beta-propeller fold called WD40. G gamma, in blue, is a smaller, all-alpha-helical protein.

A small peptide, shown in spacefilling yellow binds to beta, at the same site where G alpha binds.


Davis TL, Bonacci TM, Sprang SR, Smrcka AV.
Biochemistry. 2005 Aug 9;44(31):10593-604.

(PubMed)

1xhm (PDB)

 

Understanding molecular recognition by G protein βγ subunits on the path to pharmacological targeting.
Lin Y, Smrcka AV.
Mol Pharmacol. 2011 Oct;80(4):551-7. doi: 10.1124/mol.111.073072. Epub 2011 Jul 7. Review.
PMID: 21737569 Free PMC Article

Abstract
Heterotrimeric G proteins, composed of Gα and Gβγ subunits, transduce extracellular signals via G-protein-coupled receptors to modulate many important intracellular responses. The Gβγ subunits hold a central position in this signaling system and have been implicated in multiple aspects of physiology and the pathophysiology of disease. The Gβ subunit belongs to a large family of WD40 repeat proteins with a circular β-bladed propeller structure. This structure allows Gβγ to interact with a broad range of proteins to play diverse roles. How Gβγ interacts with and regulates such a wide variety of partners yet maintains specificity is an interesting problem in protein-protein molecular recognition in signal transduction, where signal transfer by proteins is often driven by modular conserved recognition motifs. Evidence has accumulated that one mechanism for Gβγ multitarget recognition is through an intrinsically flexible protein surface or "hot spot" that accommodates multiple modes of binding. Because each target has a unique recognition mode for Gβγ subunits, it suggests that these interactions could be selectively manipulated with small molecules, which could have significant therapeutic potential.

G protein βγ subunits: central mediators of G protein-coupled receptor signaling.
Smrcka AV.
Cell Mol Life Sci. 2008 Jul;65(14):2191-214.
Free PMC Article

Abstract
G protein betagamma subunits are central participants in G protein-coupled receptor signaling pathways. They interact with receptors, G protein alpha subunits and downstream targets to coordinate multiple, different GPCR functions. Much is known about the biology of Gbetagamma subunits but mysteries remain. Here, we will review what is known about general aspects of structure and function of Gbetagamma as well as discuss emerging mechanisms for regulation of Gbetagamma signaling. Recent data suggest that Gbetagamma is a potential therapeutic drug target. Thus, a thorough understanding of the molecular and physiological functions of Gbetagamma has significant implications.