Refinement of conformational preferences of Leu enkephalin and Tyr-Gly-Gly-Phe by 15 N n.m.r.
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1982.tb03066.x/fullpdf
Reference27 articles.
1. Preferential conformation of the endogenous opiate-like pentapeptide met-enkephalin in DMSO-d6 solution determined by high field 1H NMR
2. 1 H and 13 C NMR studies of conformational behaviour of Leu-enkephalin
3. Proton magnetic resonance studies of conformation and flexibility of enkephalin peptides
4. Conformation of Met5-enkephalin determined by high field PMR spectroscopy
5. Solution conformation of enkephalin. A nuclear magnetic resonance study of 13C-enriched carbonyl carbons in [Leu5]-enkephalin
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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. Peptide conformations. 33. Conformational analysis of cyclic enkephalin analogs of the type Tyr-cyclo-(-N ω -Xxx-Gly-Phe-Leu-)*;International Journal of Peptide and Protein Research;2009-01-12
5. Comparison of conformational properties of linear and cyclic δ selective opioid ligands DTLET (Tyr-D-Thr-Gly-Phe-Leu-Thr) and DPLPE (Tyr-c[D-Pen-Gly-Phe-Pen]) by 1H n.m.r. spectroscopy;International Journal of Peptide and Protein Research;2009-01-12
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