| Literature DB >> 10679625 |
S Capasso1, G Balboni, P Di Cerbo.
Abstract
The effect of lysine residues on the deamidation reaction of the asparagine side chain has been studied on the peptide and on its lysine-acetylated derivative in a wide range of pH values. The amino acid sequence of these peptides is similar to the local sequence flanking the labile Asn-67 in RNAse A. The experimental data show that Lys influences both the deamidation rate and the relative yield of the two reaction products, i.e., the aspartic acid and beta-aspartic acid containing peptide. These effects are pH dependent and can be rationalized based on the mechanism previously proposed for the deamidation reaction via succinimide derivative. Copyright 2000 John Wiley & Sons, Inc.Entities:
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Year: 2000 PMID: 10679625 DOI: 10.1002/(SICI)1097-0282(200002)53:2<213::AID-BIP11>3.0.CO;2-C
Source DB: PubMed Journal: Biopolymers ISSN: 0006-3525 Impact factor: 2.505