Title of article
Methyltrypsin-Catalyzed Peptide Coupling: Comparison of Alkyl Ester and Guanidinophenyl Ester Derivatives as Acyl Donor Component
Author/Authors
Itoh، نويسنده , , Kunihiko and Sekizaki، نويسنده , , Haruo and Toyota، نويسنده , , Eiko and Tanizawa، نويسنده , , Kazutaka، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1997
Pages
13
From page
307
To page
319
Abstract
Methyltrypsin-catalyzed peptide synthesis has been studied by using conventional alkyl ester andp-guanidinophenyl ester derivatives of α-amino acid as the acyl donor component. They were found to be coupled with α-amino acid derivatives (acyl acceptor component) to produce dipeptide. The behavior of methyltrypsin toward both the substrates has been studied.
Journal title
Bioorganic Chemistry: an International Journal
Serial Year
1997
Journal title
Bioorganic Chemistry: an International Journal
Record number
1385236
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