| Literature DB >> 21199869 |
Chih-chin Huang1, John J G Tesmer.
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.Entities:
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Year: 2011 PMID: 21199869 PMCID: PMC3048657 DOI: 10.1074/jbc.R109.051847
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157