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History
- Received January 22, 2019
- Accepted June 13, 2019
- Published online September 30, 2019.
Article Versions
- Earlier version (July 10, 2019 - 10:01).
- You are viewing the most recent version of this article.
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Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics
Author Information
- Irina G. Tikhonova,
- Veronique Gigoux, and
- Daniel Fourmy
- School of Pharmacy, Medical Biology Centre, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom, (I.G.T.) and INSERM ERL1226-Receptology and Therapeutic Targeting of Cancers, Laboratoire de Physique et Chimie des Nano-Objets, CNRS UMR5215-INSA, Université de Toulouse III, Toulouse, France (V.G., D.F.)
- Address correspondence to:
Dr. Irina G. Tikhonova, School of Pharmacy, Medical Biology Centre, 97 Lisburn Road, Queen’s University Belfast, Belfast BT9c7BL, Northern Ireland, United Kingdom. E-mail: i.tikhonova{at}qub.ac.uk
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- Article
- Abstract
- Introduction
- X-Ray Structures of GPCRs Bound to Peptides
- Class A Receptor Grouping with Peptide SAR and Hydrophilic Binding Site Residues as a Basis
- GPCRs Binding Peptides with the C-Terminal Free Carboxyl Group Interacting with the Helical Cavity
- GPCRs Binding Peptides with the C-Terminal Amidated Carboxyl Group Interacting with the Helical Cavity
- GPCRs Binding Peptides with the N-Terminal End Pointing to the Helical Bundle
- GPCRs Binding Cyclic Peptides with a Cyclic Part Important for Activity and the PAR Receptors
- Concluding Remarks
- Acknowledgments
- Authorship Contributions
- Footnotes
- Abbreviations
- References
- Figures & Data
- Info & Metrics
- eLetters
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