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The Journal of Biological Chemistry|October 26, 2012
Crystal structure of a voltage-gated K+ channel pore module in a closed state in lipid membranesJose S Santos, Guillermo A Asmar-Rovira, Gye Won Han, et al.Cell Discovery|February 27, 2023
The activation mechanism and antibody binding mode for orphan GPR20Xi Lin, Shan Jiang, Yiran Wu, et al.Molecular Genetics and Metabolism|July 12, 2005
Structure-based chemical modification strategy for enzyme replacement treatment of phenylketonuriaLin Wang, Alejandra Gamez, Christineh N Sarkissian, et al.Nature|May 3, 2013
Structure of the human smoothened receptor bound to an antitumour agentChong Wang, Huixian Wu, Vsevolod Katritch, et al.Structure (London, England : 1993)|February 4, 2018
Structural Connection between Activation Microswitch and Allosteric Sodium Site in GPCR SignalingKate L White, Matthew T Eddy, Zhan-Guo Gao, et al.The Journal of Biological Chemistry|July 27, 2006
Structural and biophysical characterization of the EphB4*ephrinB2 protein-protein interaction and receptor specificityJill E Chrencik, Alexei Brooun, Michelle L Kraus, et al.Structure (London, England : 1993)|November 4, 2015
The Importance of Ligand-Receptor Conformational Pairs in Stabilization: Spotlight on the N/OFQ G Protein-Coupled ReceptorRebecca L Miller, Aaron A Thompson, Claudio Trapella, et al.Cell Reports|December 5, 2019
Structural Basis of the Diversity of Adrenergic ReceptorsLu Qu, Qingtong Zhou, Yueming Xu, et al.Biochemistry|March 26, 2011
Structural characterization of three novel hydroxamate-based zinc chelating inhibitors of the Clostridium botulinum serotype A neurotoxin light chain metalloprotease reveals a compact binding site resulting from 60/70 loop flexibilityAaron A Thompson, Guan-Sheng Jiao, Seongjin Kim, et al.Nature|June 24, 2011
Structure of the human histamine H1 receptor complex with doxepinTatsuro Shimamura, Mitsunori Shiroishi, Simone Weyand, et al.Pageof 14