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Anne Imberty

Researcher at University of Grenoble

Publications -  406
Citations -  20811

Anne Imberty is an academic researcher from University of Grenoble. The author has contributed to research in topics: Lectin & Binding site. The author has an hindex of 74, co-authored 381 publications receiving 18759 citations. Previous affiliations of Anne Imberty include Bar-Ilan University & Joseph Fourier University.

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Modeling of arabinofuranose and arabinan, II. Nmr and Conformational analysis of arabinobiose and arabinan

TL;DR: In this paper, both the puckering of the arabinofuranose, rings and the orientations about the glycosidic torsion angles ϕ, ψ, and ω were considered.
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Conformational behavior of chondroitin and chondroitin sulfate in relation to their physical properties as inferred by molecular modeling.

TL;DR: The ability of coordination with cations has been explored, resulting in a preferential stereospecificity for calcium ions when compared to sodium ions, and several helical conformations correspond to the experimentally observed ones.
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Anti-biofilm Agents against Pseudomonas aeruginosa: A Structure-Activity Relationship Study of C-Glycosidic LecB Inhibitors.

TL;DR: Six new carboxamides and 24 new sulfonamides are designed and synthesized for a detailed structure–activity relationship for two clinically representative LecB variants and it is shown that modification of the sulfonamide residue bears future optimization potential.
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Crystal structure of Pterocarpus angolensis lectin in complex with glucose, sucrose and turanose

TL;DR: The crystal structure of the Man/Glc-specific seed lectin from Pterocarpus angolensis was determined in complex with methyl-α-d-glucose, sucrose, and turanose and found that glucose binding in the primary binding site is reminiscent of the glucose complexes of concanavalin A and lentil lectin.
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Conformational studies of the O-specific polysaccharide of Shigella flexneri 5a and of four related synthetic pentasaccharide fragments using NMR and molecular modeling.

TL;DR: The NMR study, based on the analysis of 1H and 13C chemical shifts, the evaluation of inter-residue distances, and the measurement of one- and three-bond heteronuclear coupling constants, showed that the conformation of one of the four pentasaccharides is similar to that of the native O-SP in solution.