Abstract
The secretin-like (class B) family of G protein-coupled receptors (GPCRs) are key players in hormonal homeostasis and are interesting drug targets for the treatment of several metabolic disorders (such as type 2 diabetes, osteoporosis, and obesity) and nervous system diseases (such as migraine, anxiety, and depression). The recently solved crystal structures of the transmembrane domains of the human glucagon receptor and human corticotropin-releasing factor receptor 1 have opened up new opportunities to study the structure and function of class B GPCRs. The current review shows how these structures offer more detailed explanations to previous biochemical and pharmacological studies of class B GPCRs, and provides new insights into their interactions with ligands. © 2013 Elsevier Ltd. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 12-22 |
| Journal | Trends in Pharmacological Sciences |
| Volume | 35 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Fingerprint
Dive into the research topics of 'New insights into the structure of Class B G protein-coupled receptors'. Together they form a unique fingerprint.Datasets
-
Secretin-like class B G protein-coupled receptor (GPCR) mutation data set
de Graaf, C. (Contributor), Unknown, 1 Jan 2014
DOI: 10.5281/zenodo.60790, https://zenodo.org/record/60790
Dataset / Software: Dataset
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver