CanN-methylated amino acids serve as substitutes for prolines in conformational design of cyclic pentapeptides?-Reference-Cited by-同舟云学术

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CanN-methylated amino acids serve as substitutes for prolines in conformational design of cyclic pentapeptides?

Published:2009-03 Issue:3 Volume:15 Page:141-146
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Pept. Sci.

Author:

Laufer Burkhardt,Chatterjee Jayanta,Frank Andreas O.,Kessler Horst

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference57 articles.

1. Solid-state geometry and conformation of linear, diastereoisomeric oligoprolines;Benedetti;Biopolymers,1983

2. Proline residues in transmembrane helices: structural or dynamic role?;Williams;Biochemistry,1991

3. Influence of proline residues on protein conformation;MacArthur;J. Mol. Biol.,1991

4. Proline-dependent structural and biological properties of peptides and proteins;Yaron;Crit. Rev. Biochem. Mol. Biol.,1993

5. Peptide flexibility and calculations of an ensemble of molecules;Mierke;J. Am. Chem. Soc.,1994

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