Structure of class B GPCR corticotropin-releasing factor receptor 1
doi: 10.1038/nature12357
pmid: 23863939
Structure of class B GPCR corticotropin-releasing factor receptor 1
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.
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
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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