His primary areas of study are G protein-coupled receptor, Receptor, Biochemistry, Stereochemistry and Biophysics. His studies in G protein-coupled receptor integrate themes in fields like Adenosine receptor, Allosteric regulation and Transmembrane domain. His Receptor research focuses on Docking and how it relates to Antagonist, Angiotensin II and Femtosecond.
Vadim Cherezov interconnects Ligand, Agonist, Protein structure, Metabotropic glutamate receptor 5 and Binding site in the investigation of issues within Stereochemistry. Vadim Cherezov has included themes like Crystallography, Structural biology, Heterotrimeric G protein, G protein and Allosteric modulator in his Biophysics study. His Structural biology course of study focuses on Mesophase and Membrane protein.
Vadim Cherezov mainly focuses on G protein-coupled receptor, Receptor, Crystallography, Membrane protein and Biochemistry. His G protein-coupled receptor research is multidisciplinary, incorporating elements of Computational biology, Stereochemistry and Allosteric regulation. The study incorporates disciplines such as Protein structure and Docking in addition to Receptor.
His work carried out in the field of Crystallography brings together such families of science as Phase, Femtosecond, X-ray crystallography and Membrane, Lipid bilayer. His Membrane protein research is multidisciplinary, relying on both Biophysics, Mesophase, Crystallization and Structural biology. His work on Cholesterol and Adenosine receptor as part of general Biochemistry study is frequently connected to Protein domain, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Vadim Cherezov mostly deals with Receptor, G protein-coupled receptor, Ligand, Computational biology and Biophysics. His biological study spans a wide range of topics, including Melatonin, Virtual screening and Protein structure. His G protein-coupled receptor research integrates issues from Subtype selectivity, Peptidomimetic, Stereochemistry and Drug discovery.
His research integrates issues of Vesicle, Phase, Liquid ordered phase, Adenosine A2A receptor and Membrane protein in his study of Ligand. Vadim Cherezov has researched Computational biology in several fields, including Docking, SUPERFAMILY, GPCR Signaling, Function and Functional selectivity. His Biophysics research includes themes of Allosteric modulator, Membrane, Transmembrane domain and Adenosine receptor.
His scientific interests lie mostly in Receptor, Pharmacology, Protein structure, Membrane protein and Agonist. The various areas that he examines in his Receptor study include Melatonin and Biophysics. His studies in Protein structure integrate themes in fields like Prostaglandin E and Prostaglandin E2 receptor.
He studied Membrane protein and Ligand that intersect with Zafirlukast and Pranlukast. The Agonist study combines topics in areas such as Chronic pain, Small molecule, Peptide and Opioid. His Melatonin receptor study frequently links to other fields, such as G protein-coupled receptor.
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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.
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.
Structural Basis for Allosteric Regulation of GPCRs by Sodium Ions
Wei Liu;Eugene Chun;Aaron A. Thompson;Pavel Chubukov.
Structure of an Agonist-Bound Human A2A Adenosine Receptor
Fei Xu;Huixian Wu;Vsevolod Katritch;Gye Won Han.
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