Structural basis of ligand interaction with atypical chemokine receptor 3-Reference-Cited by-同舟云学术

Structural basis of ligand interaction with atypical chemokine receptor 3

Published:2017-01-18 Issue:1 Volume:8 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Gustavsson Martin,Wang Liwen,van Gils Noortje,Stephens Bryan S.,Zhang Penglie,Schall Thomas J.,Yang Sichun^ORCID,Abagyan Ruben,Chance Mark R.,Kufareva Irina^ORCID,Handel Tracy M.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms14135.pdf

Reference68 articles.

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2. Nibbs, R. J. & Graham, G. J. Immune regulation by atypical chemokine receptors. Nat. Rev. Immunol. 13, 815–829 (2013).

3. Burns, J. M. et al. A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development. J. Exp. Med. 203, 2201–2213 (2006).

4. Rajagopal, S. et al. Beta-arrestin- but not G protein-mediated signaling by the ‘decoy’ receptor CXCR7. Proc. Natl Acad. Sci. USA 107, 628–632 (2010).

5. Miao, Z. et al. CXCR7 (RDC1) promotes breast and lung tumor growth in vivo and is expressed on tumor-associated vasculature. Proc. Natl Acad. Sci. USA 104, 15735–15740 (2007).

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