2020 - Fellow of the American Association for the Advancement of Science (AAAS)
1956 - Fellow of the American Association for the Advancement of Science (AAAS)
His scientific interests lie mostly in G protein-coupled receptor, Receptor, Biochemistry, Stereochemistry and Protein structure. His G protein-coupled receptor research is multidisciplinary, incorporating perspectives in Crystallography, Computational biology and Transmembrane domain. His Receptor study which covers Docking that intersects with Antagonist.
His work deals with themes such as Biophysics and Cholera toxin, which intersect with Biochemistry. His Stereochemistry research is multidisciplinary, incorporating elements of Ligand, Agonist, Active site, Structure–activity relationship and Binding site. His Protein structure study incorporates themes from Amino acid, Lipid bilayer and Helix.
Raymond C. Stevens spends much of his time researching Biochemistry, Stereochemistry, G protein-coupled receptor, Receptor and Crystallography. In his study, which falls under the umbrella issue of Stereochemistry, Peptide sequence is strongly linked to Protein structure. His work in G protein-coupled receptor tackles topics such as Computational biology which are related to areas like Structural biology.
His study looks at the relationship between Receptor and topics such as Biophysics, which overlap with Membrane protein. The various areas that Raymond C. Stevens examines in his Crystallography study include Crystallization and Molecule. The Crystal structure study combines topics in areas such as Thermotoga maritima and Resolution.
Raymond C. Stevens mainly investigates Receptor, G protein-coupled receptor, Biophysics, Computational biology and Cell biology. His research integrates issues of Protein structure and Peptide in his study of Receptor. His work carried out in the field of G protein-coupled receptor brings together such families of science as Allosteric regulation, Drug discovery and Ligand.
His Ligand research includes themes of Docking, Stereochemistry, Adrenergic receptor, Crystallography and Melatonin receptor. His Biophysics research includes elements of Peptide sequence, Glucagon-like peptide 1 receptor, Intracellular and Binding site. His work in the fields of Extracellular, Arrestin beta 2 and Phosphorylation overlaps with other areas such as Beta-2 adrenergic receptor.
The scientist’s investigation covers issues in G protein-coupled receptor, Receptor, Allosteric regulation, Biophysics and Cell biology. His G protein-coupled receptor study integrates concerns from other disciplines, such as Transmembrane domain, Inverse agonist, Computational biology and Drug discovery. His Drug discovery study is associated with Biochemistry.
His Receptor study combines topics in areas such as Melatonin, Function and Peptide. His Biophysics research incorporates themes from Protein structure, Glucagon-like peptide 1 receptor, Intracellular and Binding site. His Binding site study combines topics from a wide range of disciplines, such as Cannabinoid, Stereochemistry and Partial agonist.
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High-Resolution Crystal Structure of an Engineered Human β2-Adrenergic G Protein–Coupled Receptor
Vadim Cherezov;Daniel M. Rosenbaum;Michael A. Hanson;Søren G. F. Rasmussen.
The 2.6 Angstrom Crystal Structure of a Human A2A Adenosine Receptor Bound to an Antagonist.
Veli-Pekka Jaakola;Mark T. Griffith;Michael A. Hanson;Vadim Cherezov.
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists.
Beili Wu;Ellen Y. T. Chien;Clifford D. Mol;Gustavo Fenalti.
GPCR Engineering Yields High-Resolution Structural Insights into β2-Adrenergic Receptor Function
Daniel M. Rosenbaum;Vadim Cherezov;Michael A. Hanson;Søren G. F. Rasmussen.
Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity.
C U Kim;W Lew;M A Williams;H Liu.
Journal of the American Chemical Society (1997)
Structure of the human dopamine d3 receptor in complex with a d2/d3 selective antagonist.
Ellen Y. T. Chien;Wei Liu;Qiang Zhao;Vsevolod Katritch.
Structure-Function of the G Protein–Coupled Receptor Superfamily
Vsevolod Katritch;Vadim Cherezov;Raymond C. Stevens.
Annual Review of Pharmacology and Toxicology (2013)
A specific cholesterol binding site is established by the 2.8 A structure of the human beta2-adrenergic receptor.
Michael A. Hanson;Vadim Cherezov;Mark T. Griffith;Christopher B. Roth.
Structure of the human κ-opioid receptor in complex with JDTic
Huixian Wu;Daniel Wacker;Mauro Mileni;Vsevolod Katritch.
Crystal structure of botulinum neurotoxin type A and implications for toxicity.
D B Lacy;W Tepp;A C Cohen;B R DasGupta.
Nature Structural & Molecular Biology (1998)
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