Abstract
Class B GPCRs of the secretin family are important drug targets in many human diseases including diabetes, neurodegeneration, cardiovascular disease and psychiatric disorders. X-ray crystal structures for the glucagon receptor and corticotropin-releasing factor receptor 1 have now been published. In this review, we analyse the new structures and how they compare with each other and with Class A and F receptors. We also consider the differences in druggability and possible similarity in the activation mechanisms. Finally, we discuss the potential for the design of small-molecule modulators for these important targets in drug discovery. This new structural insight allows, for the first time, structure-based drug design methods to be applied to Class B GPCRs. © 2014 The British Pharmacological Society.
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Bortolato, A., Doré, A. S., Hollenstein, K., Tehan, B. G., Mason, J. S., & Marshall, F. H. (2014). Structure of Class B GPCRs: New horizons for drug discovery. British Journal of Pharmacology. John Wiley and Sons Inc. https://doi.org/10.1111/bph.12689
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