Abstract
1H- and 13C-NMR assignments for the carbohydrate part of the glycopeptide alpha-d-Man-(1->6)-[ß-d-Xyl-(1->2)]-ß-d-Man-(1->4)-ß-d-GlcNAc-(1->4)-[alpha-l-Fuc-(1->3)]-ß-d- GlcNAc-(1->N)-Asn~, derived from the proteolytic enzyme bromelain (EC 3.4.22.4), have been obtained using homo- and heteronuclear correlation spectroscopy, two-dimensional homonuclear Hartmann-Hahn and nuclear Overhauser enhancement experiments. A conformational model for the carbohydrate chain, deduced from the NMR data
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