Ab Initio Study of Lowest-Energy Conformers of Lewis X (Lex) Trisaccharide
- 22 March 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 104 (15) , 3381-3390
- https://doi.org/10.1021/jp9935034
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Theoretical Study of Alternative Ring Forms of α-l-FucopyranoseThe Journal of Physical Chemistry A, 1998
- Crystal and molecular structure of a histo-blood group antigen involved in cell adhesion: the Lewis x trisaccharideGlycobiology, 1996
- A comparison of conformational energies calculated by several molecular mechanics methodsJournal of Computational Chemistry, 1996
- Experimental Evidence of Conformational Differences betweenC-Glycosides andO-Glycosides in Solution and in the Protein-Bound State: TheC-Lactose/O-Lactose CaseJournal of the American Chemical Society, 1996
- Structure--function studies on selectin carbohydrate ligands. Modifications to fucose, sialic acid and sulphate as a sialic acid replacementGlycobiology, 1993
- Quantum chemical conformational analysis of glucose in aqueous solutionJournal of the American Chemical Society, 1993
- Ab Initio computed molecular structures and energies of the conformers of glucoseJournal of Computational Chemistry, 1992
- Solution structure of the Lewis x oligosaccharide determined by NMR spectroscopy and molecular dynamics simulationsBiochemistry, 1992
- Synthesis and structural analysis using 2-D NMR of sialyl Lewis X (SLex) and Lewis X (Lex) oligosaccharides: ligands related to E-selectin [ELAM-1] binding.Journal of the American Chemical Society, 1992
- Sticky sugars for selectinsNature, 1991