The Lipid Pathway of Protein Glycosylation and its Inhibitors: The Biological Significance of Protein-Bound Carbohydrates
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2012, The Biochemistry of Plants: A Comprehensive TreatiseN-glycans in cell survival and death: Cross-talk between glycosyltransferases
2012, Biochimica et Biophysica Acta - General SubjectsCitation Excerpt :Dol-P-Man also donates all three (four in yeast) mannose residues in glycophosphatidylinositol (GPI), the first mannose in O-mannosylation of many yeast proteins, O-mannosylation of mammalian proteins and in C-mannosylation of Trp-7 in human ribonuclease 2 [18-22]. Fine details of the dolicholphosphate cycle, the topography of the reactions, the subcellular localization and the inhibitors have been reviewed earlier, extensively [21,23-31]. Mannosylphospho dolichol synthase (DPMS) has recently been reviewed [32].
The Development of Carbohydrate Chemistry and Biology
2008, Carbohydrate Chemistry, Biology and Medical ApplicationsSynthesis of the sugar moiety of TIME-EA4, a glycopeptide isolated from silkworm diapause eggs
2006, Carbohydrate ResearchCitation Excerpt :The key challenges for the synthesis of N-glycans have been the construction of β-d-mannosides, which are especially difficult to accomplish since both neighboring group assistance and the anomeric effect uniformly favor the formation of α-d-mannosides during glycosylation. Methods for the construction of β-d-mannosidic linkages have been reviewed,8 and several approaches, including the intramolecular aglycon delivery9 and direct β-d-mannoside coupling protocol,10 have been reported to effectively solve this problem. Epimerizations of β-d-glucopyranosides at the C-2 position by direct SN2 inversion11 or oxidation–reduction of the C-2 hydroxyl group12 are established methods for the indirect preparation of β-d-mannosides; additionally, a two-step protocol for β-selective glycosylation using a glyco-ulosyl bromide and an acceptor, followed by manno-selective reduction of the resulting β-2-ketoglucoside, is also established.13