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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Nature
Article . 2013 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
Nature
Article . 2013
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Structure of class B GPCR corticotropin-releasing factor receptor 1

Authors: Kaspar, Hollenstein; James, Kean; Andrea, Bortolato; Robert K Y, Cheng; Andrew S, Doré; Ali, Jazayeri; Robert M, Cooke; +2 Authors

Structure of class B GPCR corticotropin-releasing factor receptor 1

Abstract

Structural analysis of class B G-protein-coupled receptors (GPCRs), cell-surface proteins that respond to peptide hormones, has been restricted to the amino-terminal extracellular domain, thus providing little understanding of the membrane-spanning signal transduction domain. The corticotropin-releasing factor receptor type 1 is a class B receptor which mediates the response to stress and has been considered a drug target for depression and anxiety. Here we report the crystal structure of the transmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the small-molecule antagonist CP-376395. The structure provides detailed insight into the architecture of class B receptors. Atomic details of the interactions of the receptor with the non-peptide ligand that binds deep within the receptor are described. This structure provides a model for all class B GPCRs and may aid in the design of new small-molecule drugs for diseases of brain and metabolism.

Keywords

Models, Molecular, Binding Sites, Amino Acid Motifs, Molecular Sequence Data, Receptors, Dopamine D3, Aminopyridines, CRF Receptor, Type 1, Crystallography, X-Ray, Ligands, Receptors, Corticotropin-Releasing Hormone, Protein Structure, Tertiary, HEK293 Cells, Humans, Amino Acid Sequence, Conserved Sequence, Protein Binding

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    387
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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
387
Top 1%
Top 1%
Top 0.1%