| Literature DB >> 31036298 |
Abstract
Protein-protein interactions are key in cellular signaling. G protein-coupled receptors (GPCRs), the largest superfamily of human membrane proteins, are able to transduce extracellular signals (e.g., hormones and neurotransmitters) to intracellular proteins, in particular the G proteins. Since GPCRs serve as primary targets of ~1/3 of currently marketed drugs, it is important to understand mechanisms of GPCR signaling in order to design selective and potent drug molecules. This chapter focuses on recent advances in computational studies of the GPCR-G protein interactions using bioinformatics, protein-protein docking and molecular dynamics simulation approaches.Entities:
Keywords: Bioinformatics; GPCR-G protein interactions; Molecular dynamics; Protein-protein docking; Protein-protein interactions
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Year: 2019 PMID: 31036298 PMCID: PMC6986689 DOI: 10.1016/bs.apcsb.2018.11.011
Source DB: PubMed Journal: Adv Protein Chem Struct Biol ISSN: 1876-1623 Impact factor: 3.507