GPCR Engineering Yields High-Resolution Structural Insights into β2-Adrenergic Receptor Function
By D. Rosenbaum, Vadim Cherezov, M. Hanson, S. Rasmussen, Foon Sun Thian, T. S. Kobilka, Hee-Jung Choi, X. Yao, William I. Weis, Raymond C. Stevens and 1 more. Science, 2007
1,308 citations recorded by the source corpus.
Subfields: Animal Science and Zoology, Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1d9ab2cb77040f9cdba6ccd8611fa39922150630
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- Raymond C. Stevens
- Vadim Cherezov
- Vsevolod Katritch
- Brian K. Kobilka
- Ruben Abagyan
- Jens Meiler
- Roderick E. Hubbard
- William I. Weis
In Molecular Biology
- Vsevolod Katritch
- Raymond C. Stevens
- Brian K. Kobilka
- Vadim Cherezov
- Ruben Abagyan
- Jens Meiler
- William I. Weis
- Brian Joseph Bender
Citations in the corpus
- GPCR Network: a large-scale collaboration on GPCR structure and function (2012, background): “Additional structure reports include the characterization of the active and inactive states for rhodopsin 36 and opsin 37 , β 2 -AR 38–41 and adenosine A 2A receptor 18,42,43 .”
- The Molecular Basis of G Protein–Coupled Receptor Activation (2018, background): “Spectroscopic studies, however, have shown that the presence of a fusion protein in ICL3 can alter conformational equilibria (19).”
- Structure-based drug discovery and protein targets in the CNS. (2011, background): “The recent breakthroughs are described in more detail below, but in summary have introduced mutations (Warne et al., 2008), an additional domain (Cherezov et al., 2007) or complexation with antibody (Rosenbaum et al., 2007).”