Allosteric Na+-binding site modulates CXCR4 activation
Author:
Affiliation:
1. Université Côte d'Azur
2. CNRS, Institut de Chimie de Nice UMR7272
3. 06108 Nice
4. France
5. Department of Brain & Cognitive Sciences
Abstract
G protein-coupled receptors (GPCRs) control most cellular communications with the environment and are the largest protein family of drug targets.
Funder
Deutsche Forschungsgemeinschaft
Agence Nationale de la Recherche
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2018/CP/C8CP04134B
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