Proteins Structure Function and Bioinformatics · 2003 · 32 citations · 28 references
Sequence entropy-variability plots based on alignments of very large numbers of sequences-can indicate the location in proteins of the main active site and modulator sites. In the previous article in this issue, we applied this observation to a series of well-studied proteins and concluded that it was possible to detect most of the residues with a known functional role. Here, we apply the method to rhodopsin-like G protein-coupled receptors. Our conclusion is that G protein binding is the main evolutionary constraint on these receptors, and that other ligands, such as agonists, act as modulators. The activation of the receptors can be described as a simple, two-step process, and the residues involved in signal transduction can be identified.
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Crystal Structure of Rhodopsin: A G Protein-Coupled Receptor
Krzysztof Palczewski, Takashi Kumasaka, Tetsuya Hori et al. · Science · 2000 · 5.6K citations
Crystal Structure, Photoreceptor Cell, Molecular Physiology +14
Juan Antonio Ballesteros‐Cánovas, Anne D. Jensen, George Liapakis et al. · Journal of Biological Chemistry · 2001 · 616 citations · Full text
Ionic Lock, Transmembrane Segments 3, Synaptic Transmission +25