Kling R, Tschammer N, Lanig H, Clark T, Gmeiner P (2014)
Publication Language: English
Publication Type: Journal article, Original article
Publication year: 2014
Publisher: Public Library of Science
Book Volume: 9
Article Number: e100069
URI: http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0100069
DOI: 10.1371/journal.pone.0100069
Partial agonists exhibit a submaximal capacity to enhance the coupling of one receptor to an intracellular binding partner. Although a multitude of studies have reported different ligand-specific conformations for a given receptor, little is known about the mechanism by which different receptor conformations are connected to the capacity to activate the coupling to G-proteins. We have now performed molecular-dynamics simulations employing our recently described active-state homology model of the dopamine D
APA:
Kling, R., Tschammer, N., Lanig, H., Clark, T., & Gmeiner, P. (2014). Active-State Model of a Dopamine D2 Receptor - Gαi Complex Stabilized by Aripiprazole-Type Partial Agonists. PLoS ONE, 9. https://doi.org/10.1371/journal.pone.0100069
MLA:
Kling, Ralf, et al. "Active-State Model of a Dopamine D2 Receptor - Gαi Complex Stabilized by Aripiprazole-Type Partial Agonists." PLoS ONE 9 (2014).
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