Structure-Based Design in the GPCR Target Space

Author(s): M. Kontoyianni, Z. Liu

Journal Name: Current Medicinal Chemistry

Volume 19 , Issue 4 , 2012

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The G protein-coupled receptors (GPCRs) are membrane proteins that transmit signals via G-protein coupling. They have long been the target of small molecule therapeutics accounting for 30% of the launched drug targets. They are subdivided into several classes, with rhodopsins corresponding to the largest class. Furthermore, a high number of new rhodopsin-like GPCR proteins are included in the druggable genome, thus they are projected to continue being of value to the pharmaceutical and biotechnology sectors. We present a comprehensive review of the structural information pertaining to GPCRs, in light of the most recently deposited crystal structures, along with comparisons of the available to-date structures at different activation states. Finally, computational approaches to GPCR modeling are discussed in conjunction with critical perspectives regarding feasibility and limitations.

Keywords: G-protein Coupled Receptors, Homology Modeling, Virtual Screening, Model-Building, Critical Assessment of Structure Prediction, Docking, Structure-Based Drug Design, Activation Mechanism, Conserved Motifs, Mutagenesis

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Article Details

Year: 2012
Page: [544 - 556]
Pages: 13
DOI: 10.2174/092986712798918824
Price: $65

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