Abstract
G protein-coupled receptors (GPCRs) represent the largest class of integral membrane protein receptors in the human genome. Despite the great diversity of ligands that activate these GPCRs, they interact with a relatively small number of intracellular proteins to induce profound physiological change. Both heterotrimeric G proteins and GPCR kinases are well known for their ability to specifically recognize GPCRs in their active state. Recent structural studies now suggest that heterotrimeric G proteins and GPCR kinases identify activated receptors via a common molecular mechanism despite having completely different folds. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Huang, C. C., & Tesmer, J. J. G. (2011, March 11). Recognition in the face of diversity: Interactions of heterotrimeric G proteins and G protein-coupled receptor (GPCR) kinases with activated GPCRs. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.R109.051847
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