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Nature|December 3, 2020
Structure of the class D GPCR Ste2 dimer coupled to two G proteinsVaithish Velazhahan, Ning Ma, Gáspár Pándy-Szekeres, et al.
Pharmacogenetics and Genomics|February 16, 2007
Interactions with other human UDP-glucuronosyltransferases attenuate the consequences of the Y485D mutation on the activity and substrate affinity of UGT1A6Mika Kurkela, Anne-Sisko Patana, Peter I Mackenzie, et al.
Plos One|April 21, 2017
Mini-G proteins: Novel tools for studying GPCRs in their active conformationRony Nehmé, Byron Carpenter, Ankita Singhal, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2011
Two distinct conformations of helix 6 observed in antagonist-bound structures of a beta1-adrenergic receptorRouslan Moukhametzianov, Tony Warne, Patricia C Edwards, et al.
Plos One|March 17, 2016
Complete Reversible Refolding of a G-Protein Coupled Receptor on a Solid SupportNatalie Di Bartolo, Emma L R Compton, Tony Warne, et al.
Nature|July 7, 2015
Universal allosteric mechanism for Gα activation by GPCRsTilman Flock, Charles N J Ravarani, Dawei Sun, et al.
Nature|January 14, 2011
The structural basis for agonist and partial agonist action on a β(1)-adrenergic receptorTony Warne, Rouslan Moukhametzianov, Jillian G Baker, et al.
Nature|October 12, 2012
Structure of the agonist-bound neurotensin receptorJim F White, Nicholas Noinaj, Yoko Shibata, et al.
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