Abstract
The rhodopsin-like superfamily of 7-transmembrane receptors is the largest class of signalling molecules in the mammalian genome. Recently, a combination of mutagenesis, biophysical and modelling studies have suggested a credible model for the α-carbon backbone in the transmembrane region of the 7-transmembrane receptors, and have started to reveal the structural basis of the conformational switch from the inactive to the active state. A key feature may be the replacement of a network of radial constraints, centred on transmembrane helix three, which stabilise the inactive ground state of the receptor by a new set of axial interactions which help to stabilise the activated state. Transmembrane helix three may act as a rotary switch in the activation mechanism. Copyright (C) 1999 Elsevier Science B.V.
Original language | English |
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Pages (from-to) | 247-260 |
Number of pages | 14 |
Journal | European Journal of Pharmacology |
Volume | 375 |
Issue number | 1-3 |
DOIs | |
Publication status | Published - 30 Jun 1999 |
Externally published | Yes |
Keywords
- 7-Transmembrane receptor
- Acetylcholine
- G-protein
- G-protein coupling pocket
- Muscarinic receptor