Influence of Chirality of the Preceding Acyl Moiety on the cis/trans Ratio of the Proline Peptide Bond-Reference-Cited by-同舟云学术

Influence of Chirality of the Preceding Acyl Moiety on the cis/trans Ratio of the Proline Peptide Bond

Published:2001-09-27 Issue:21 Volume:66 Page:7044-7050
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Breznik Matej¹,Grdadolnik Simona Golič¹,Giester Gerald¹,Leban Ivan¹,Kikelj Danijel¹

Affiliation:

1. University of Ljubljana, Faculty of Pharmacy, Aškerčeva 7, 1000 Ljubljana, Slovenia, National Institute of Chemistry, Ljubljana, Slovenia, Institut für Mineralogie und Kristallographie, Universität Wien, Austria, and University of Ljubljana, Faculty of Chemistry and Chemical Technology, Ljubljana, Slovenia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0159439

Reference60 articles.

1. Consideration of the possibility that the slow step in protein denaturation reactions is due to cis-trans isomerism of proline residues

2. Conformational energy studies of linear dipeptides H-X-L-Pro-OH

3. Nmr studies of the rates of prolinecis-transisomerization in oligopeptides

4. Occurrence and role ofcis peptide bonds in protein structures

5. Prolyl Isomerase: Enzymatic Catalysis of Slow Protein-Folding Reactions

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