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 |
|---|---|
| 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
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