Conformation-dependent O-glycosylation of threonine-containing dipeptides
✍ Scribed by N.Joe Maeji; Yoshio Inoue; Riichirô Chûjô
- Book ID
- 102641457
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 241 KB
- Volume
- 146
- Category
- Article
- ISSN
- 0008-6215
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Stepwise solution syntheses are described of the homo-oligomers Z-(Thr) n -NHCH 3 (n1±4, Members of the III 1±5 series were obtained by de-acetylation of the corresponding oligomers of the II 1±5 series. The conformational preferences of the terminally protected homo-peptides of the three series we
Enzymatic O-glycosylation of dipeptide derivatives containing a serine residue in the N or C terminal position and alanine or glycine as the second amino acid was achieved using the transgalactosylation activity of [3-galactosidase from the Achatina achatina digestive juice. Reactions were performed