Enzymatic Peptide Synthesis with p-Guanidinophenyl and p-(Guanidinomethyl)phenyl Esters as Acyl Donors. -Two series of "inverse substrates", e.g. (VII) and (IV), are prepared as acyl donor components for enzymatic peptide synthesis. These substrates are found to couple readily with amino acid p-nit
Trypsin-catalyzed peptide synthesis withm-guanidinophenyl andm-(guanidinomethyl)phenyl esters as acyl donor component
β Scribed by H. Sekizaki; K. Itoh; E. Toyota; K. Tanizawa
- Book ID
- 105167821
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 474 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0939-4451
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π SIMILAR VOLUMES
Methyltrypsin-catalyzed peptide synthesis has been studied by using conventional alkyl ester and p-guanidinophenyl ester derivatives of Ν°-amino acid as the acyl donor component. They were found to be coupled with Ν°-amino acid derivatives (acyl acceptor component) to produce dipeptide. The behavior o
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