Conformational investigation of α,β‐dehydropeptides: V. Stability of reverse turns in saturated and α,β‐unsaturated peptides Ac‐Pro‐Xaa‐NHCH3: CD studies in various solvents

International Journal of Peptide and Protein Research

Volumn 42, Issue 5, 1993, Pages 466-474

  LISOWSKI, MAREK ^a   PIETRZYŃSKI, GRZEGORZ ^b   RZESZOTARSKA, BARBARA ^b  

^a UNIVERSITY OF WROC AW   (Poland)

^b UNIVERSITY OF OPOLE   (Poland)

Author keywords

circular dichroism; conformational studies; phenylalaninc pepride CD; proline peptides; , dehydroamino acid residues; dehydropeptidc conformation; turn; turn

Indexed keywords

DEHYDROPEPTIDE; SOLVENT; SYNTHETIC PEPTIDE; UNCLASSIFIED DRUG;

ARTICLE; CIRCULAR DICHROISM; MOLECULAR STABILITY; PROTEIN CONFORMATION;

CIRCULAR DICHROISM; COMPARATIVE STUDY; DIPEPTIDES; PROTEIN CONFORMATION; SOLVENTS; STEREOISOMERISM; SUPPORT, NON-U.S. GOV'T;

EID: 0027443901     PISSN: 03678377     EISSN: 13993011     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1993.tb00156.x     Document Type: Article

References (47)

1. Experimental investigations on the backbone folding of proline-containing model tripeptides
2. Nuclear Overhauser effects and circular dichroism as probes of .beta.-turn conformations in acyclic and cyclic peptides with pro-X sequences
3. Proton magnetic resonance studies in trifluoroethanol. Solvent mixtures as a means of delineating peptide protons
4. Solution conformation and synthesis of a linear heptapeptide containing two dehydrophenylalanine residues separated by three L-amino acids