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ASN-GlcNAc

A/ -(2-Acetamido-2-deoxy-p-D-glucopyranosyl)-L-asparagine [(GlcNAc-)Asn] or 2-acetamido-A/ -L-P-aspartyl-2-deoxy-p-D-glucopyranosylamine (trivial name p-W-acetylglucosaminyl-L-asparagine)... [Pg.138]

A conformational analysis, by NMR and molecular dynamics,116 of a cyclic C-glycosyl analogue of p-GlcNAc-Asn demonstrated some variations in relation to the conformation of the regular A-glycosyl analogue. [Pg.279]

Linked structure, NeuAc(a2-3)Gal(31-3)[NeuAc(a2-6)]GalNac(al-G)Ser/Thr, N-Linked structure, [NeuAc(a2-3)Gal-GlcNAc-Man]2-Man-GlcNAc-GlcNAc-Asn. [Pg.437]

Glycopeptides are more difficult to synthesize than the conventional peptides, because common protection-deprotection reactions used in the peptide synthesis can cause serious problems to the protective groups used for carbohydrates. Many of these problems have been solved by recent technical innovations [21]. The combination of 9-fluorenylmethyloxycarbonyl (Fmoc) group for N-protection and pentafluo-rophenyl (PFP) group as the activating group for the carboxylic acid allows GlcNAc-Asn... [Pg.613]

See other pages where ASN-GlcNAc is mentioned: [Pg.289]    [Pg.289]    [Pg.289]    [Pg.289]    [Pg.518]    [Pg.62]    [Pg.62]    [Pg.62]    [Pg.10]    [Pg.267]    [Pg.408]    [Pg.344]    [Pg.295]    [Pg.1159]    [Pg.235]    [Pg.238]    [Pg.244]    [Pg.182]    [Pg.217]    [Pg.412]    [Pg.1217]    [Pg.800]    [Pg.1418]    [Pg.1829]    [Pg.161]    [Pg.790]    [Pg.185]    [Pg.185]    [Pg.186]    [Pg.187]    [Pg.613]    [Pg.229]    [Pg.315]    [Pg.318]    [Pg.551]    [Pg.246]    [Pg.225]    [Pg.296]    [Pg.296]    [Pg.299]    [Pg.299]    [Pg.301]    [Pg.2]   
See also in sourсe #XX -- [ Pg.494 ]



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GlcNAc

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