Identification of monellin as the first naturally derived proteinaceous allosteric agonist of metabotropic glutamate receptor 5
Allosteric modulators bind sites distinct from orthosteric ligands, allowing for improved spatiotemporal control of receptors and greater subtype selectivity. However, we recently showed that allosteric ligands previously classified as selective for select Class C G protein‐coupled receptors (GPCRs)...
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Veröffentlicht in: | Basic & clinical pharmacology & toxicology 2020-06, Vol.126 (S6), p.104-115 |
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Sprache: | eng |
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