Literature DB >> 6696760

Nucleophile specificity in chymotrypsin peptide synthesis.

D D Petkov, I Stoineva.   

Abstract

The partitioning of the acylenzyme acetyl-(Gly)n-Phe(NO2)-chymotrypsin (n = 0,1,2) to peptide and peptide acid is observed spectrophotometrically. Values of partitioning ratios for various nucleophiles are calculated from the spectral data. They are a measure for the "true" nucleophile reactivity and are useful in the prediction of the best experimental conditions in enzymic peptide synthesis. A large difference in the nucleophile reactivity is observed which is attributed to the S'2-P'2 interaction.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6696760     DOI: 10.1016/0006-291x(84)91103-3

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  gamma-Glutamyltranspeptidase-catalysed acyl-transfer to the added acceptor does not proceed via the ping-pong mechanism.

Authors:  R C Bateman
Journal:  Biochem J       Date:  1994-12-15       Impact factor: 3.857

2.  Glycine flanked by hydrophobic bulky amino acid residues as minimal sequence for effective subtilisin catalysis.

Authors:  E K Bratovanova; D D Petkov
Journal:  Biochem J       Date:  1987-12-15       Impact factor: 3.857

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.