[Conformation of glycopeptides with L- and D-stereoisomers of Ala and Glu amino acids].

Abstract

On the base of the semi-empirical method of conformational analysis low-energetic conformations have been found for the glycopeptides with the O-beta-N-acetyl-D-muramic acid or the O-beta-N-acetyl--D-glucosaminyl-(1-4)-N-acetyl-D-muramic acid in the glycan part and L-Ala--D-GluNH2, L-Ala--L-GluNH2, D-Ala--D-GluNH2 in the peptide part. It was shown that for either molecule preferentiability of any conformation is determined mainly by interactions between dipeptide and muramic acid residue.

Cite this paper

@article{Maksumov1985ConformationOG, title={[Conformation of glycopeptides with L- and D-stereoisomers of Ala and Glu amino acids].}, author={I. S. Maksumov and L. I. Ismailova and N M Godzhaev}, journal={Molekuliarnaia biologiia}, year={1985}, volume={19 3}, pages={730-41} }