Synthesis of a new β-amino acid with a 3-deoxy-l-ara furnaoside side chain: the influence of the side chain on the conformation of α/β-peptides
Author:
Affiliation:
1. Organic and Biomolecular Chemistry Division
2. CSIR-Indian Institute of Chemical Technology
3. Hyderabad 500 007
4. India
5. Centre for Nuclear Magnetic Resonance
Abstract
The α/β-peptides from a new C-linked carbo β-amino acid, [(R)-β-Caa(da)], with a 3-deoxy-l-ara furanoside side chain, alternatingly with d-Ala, formed left-handed 11/19-helices.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/OB/C5OB01753J
Reference48 articles.
1. Conformational parameters for amino acids in helical, β-sheet, and random coil regions calculated from proteins
2. Empirical Predictions of Protein Conformation
3. The interrelationships of side-chain and main-chain conformations in proteins
4. Side-chain control of beta-peptide secondary structures. Design principles
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