What is he best known for?
The fields of study he is best known for:
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.
His most cited work include:
- High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor. (2718 citations)
- The 2.6 Angstrom Crystal Structure of a Human A2A Adenosine Receptor Bound to an Antagonist. (1500 citations)
- Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists. (1391 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Biochemistry (28.25%)
- Stereochemistry (27.37%)
- G protein-coupled receptor (26.14%)
What were the highlights of his more recent work (between 2015-2021)?
- Receptor (25.61%)
- G protein-coupled receptor (26.14%)
- Biophysics (13.51%)
In recent papers he was focusing on the following fields of study:
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.
Between 2015 and 2021, his most popular works were:
- Crystal Structure of the Human Cannabinoid Receptor CB2. (310 citations)
- Crystal Structure of the Human Cannabinoid Receptor CB2. (310 citations)
- How Ligands Illuminate GPCR Molecular Pharmacology. (221 citations)
In his most recent research, the most cited papers focused on:
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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