Uncertainties in structural determinations of oligosaccharide conformation, using measurements of nuclear Overhauser effects
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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1. Structural analysis of a glycolipid head group with one- and two-state NMR pseudoenergy approaches
2. Solution conformations of N-linked oligosaccharides
3. Synthetic receptor analogues: the conformation of methyl 4-O-α-d-galactopyranosyl-β-d-galactopyranoside (methyl β-d-galabioside) and related derivatives, determined by N.M.R. and computational methods
4. Hydroxyl and amido groups as long-range sensors in conformational analysis by nuclear Overhauser enhancement: a source of experimental evidence for conformational flexibility of oligosaccharides
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1. NMR structural biology of sulfated glycans;Journal of Biomolecular Structure and Dynamics;2016-08-05
2. The Conformational Properties of the Glc3Man Unit Suggest Conformational Biasing within the Chaperone-assisted Glycoprotein Folding Pathway;Journal of Molecular Biology;2009-03
3. GLYCAM06: A generalizable biomolecular force field. Carbohydrates;Journal of Computational Chemistry;2007-09-11
4. The Application of Molecular Modeling Techniques to the Determination of Oligosaccharide Solution Conformations;Reviews in Computational Chemistry;2007-01-05
5. The importance of including local correlation times in the calculation of inter-proton distances from NMR measurements: ignoring local correlation times leads to significant errors in the conformational analysis of the Glcα1–2Glcα linkage by NMR spectroscopy;Org. Biomol. Chem.;2006
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