Synthesis and NMR conformational analysis of a β-turn mimic incorporated into gramicidin S
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1991.tb01510.x/fullpdf
Reference54 articles.
1. 2,8-Dimethyl-4-(carboxymethyl)-6-(aminomethyl)phenoxathiin S-dioxide: an organic substitute for the .beta.-turn in peptides?
2. Methodology for the synthesis of mimetics of peptide β-turns
3. A convenient preparation of derivatives of 3(s)-amino-10(r)-carboxy-1,6-diaza-cyclodeca-2,7-dione the dilactam of L-α, γ-diaminobutyric acid and d-glutamic acid: A β-turn template
4. Three novel mimics for the construction of sterically constrained protein turn models
5. Chain-folding initiation structures in ribonuclease A: conformational free energy calculations on Ac-Asn-Pro-Tyr-NHMe, Ac-Tyr-Pro-Asn-NHMe, and related peptides
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