
pmid: 15094833
A model for interaction of class A G protein-coupled receptor with the G protein G(alpha) subunit is proposed using the rhodopsin-transducin (RD/Gt) prototype. The model combines the resolved interactions/distances, essential in the active RD*/Gt system, with the structure of Gt(alpha) C-terminal peptide bound to RD* while stabilizing it. Assuming the interactions involve conserved parts of the partners, the model specifies the conserved Helix 2 non-polar X- - -X, Helix 3 DRY and Helix 7/8 NP- -Y- - F RD* motifs interacting with the Gt(alpha) C-terminal peptide, in compliance with the structure of the latter. A concomitant role of Gt(alpha) and Gt(gamma) C-termini in stabilizing RD* could possibly be resolved assuming a receptor dimer as requisite for G protein activation.
GPCR class A, Models, Molecular, Rhodopsin, Binding Sites, Protein Conformation, Static Electricity, Membrane Proteins, G protein, Darkness, Receptors, G-Protein-Coupled, Amino Acid Substitution, Drug Stability, GTP-Binding Proteins, Retinaldehyde, GPCR activation, Transducin, Conserved Sequence
GPCR class A, Models, Molecular, Rhodopsin, Binding Sites, Protein Conformation, Static Electricity, Membrane Proteins, G protein, Darkness, Receptors, G-Protein-Coupled, Amino Acid Substitution, Drug Stability, GTP-Binding Proteins, Retinaldehyde, GPCR activation, Transducin, Conserved Sequence
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