| Literature DB >> 1667378 |
L H Zang1, A M Howseman, R G Shulman.
Abstract
Assignments of nearly all the 1H chemical shifts of glycogen are made by 2-D 1H-1H homonuclear and 13C-1H heteronuclear COSY. We demonstrated that it is possible to obtain well-resolved 2-D n.m.r. spectra for a large molecule like glycogen. The seven nonequivalent protons of the glucose residues in the alpha-(1----4)-linked chains, and of those at the nonreducing ends, were completely assigned. Distinct chemical shifts for H-1 and H-2 immediately adjacent to the alpha-(1----6) bonds at the branch points were also determined. Several modifications of previous 13C chemical shift assignments were made from the heteronuclear 2-D n.m.r. data.Entities:
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Year: 1991 PMID: 1667378 DOI: 10.1016/0008-6215(91)80001-4
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104