The probability distribution of side-chain conformations in [Leu] and [Met]enkephalin determines the potency and selectivity to μ and δ opiate receptors
Author:
Publisher
Wiley
Subject
Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics
Reference44 articles.
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1. Gas-phase structures reflect the pain-relief potency of enkephalin peptides;Physical Chemistry Chemical Physics;2019
2. Cold ion spectroscopy for structural identifications of biomolecules;International Reviews in Physical Chemistry;2018-10-02
3. Theoretical conformational analysis of opiate peptides Leu-Enkephalin (H-Tyr-Gly-Gly-Phe-Leu-OH) and its two thioamide analogs (H-Tyr-Glyψ[CSNH]Gly-Phe-Leu-OH) and (H-Tyr-Gly-Glyψ[CSNH]Phe-Leu-OH);Structural Chemistry;2017-11-04
4. Nonstatistical UV Fragmentation of Gas-Phase Peptides Reveals Conformers and Their Structural Features;The Journal of Physical Chemistry Letters;2016-03-08
5. Resonance Energy Transfer Relates the Gas-Phase Structure and Pharmacological Activity of Opioid Peptides;Angewandte Chemie International Edition;2015-11-13
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