Literature DB >> 16592548

Internal charge transfer in proteins to the Schiff bases of their lysine side chains.

P Otto1, J Ladik, K Laki, A Szent-Györgyi.   

Abstract

Stereochemical investigations carried out with the aid of molecular models show that the Schiff bases formed between methylglyoxal and the primary amino groups of the lysine side chains of proteins can bend back in such a way to the N atoms of the peptide groups that a charge transfer can occur between these groups and the oxygen atoms of the Schiff bases. Ab initio molecular orbital calculations support this finding.

Entities:  

Year:  1978        PMID: 16592548      PMCID: PMC392820          DOI: 10.1073/pnas.75.8.3548

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  2 in total

1.  Electronic properties of the casein-methylglyoxal complex.

Authors:  R Pethig; A Szent-Györgyi
Journal:  Proc Natl Acad Sci U S A       Date:  1977-01       Impact factor: 11.205

2.  Electronic properties of some protein--methylglyoxal complexes.

Authors:  S Bone; T J Lewis; R Pethig; A Szent-Györgyi
Journal:  Proc Natl Acad Sci U S A       Date:  1978-01       Impact factor: 11.205

  2 in total
  2 in total

1.  Quantum chemical calculations of model systems for ascorbic acid adducts with Schiff bases of lysine side chains: possibility of internal charge transfer in proteins.

Authors:  P Otto; J Ladik; A Szent-Györgyi
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

2.  Spectroscopic studies of the protein-methylglyoxal adduct.

Authors:  J A McLaughlin; R Pethig; A Szent-Györgyi
Journal:  Proc Natl Acad Sci U S A       Date:  1980-02       Impact factor: 11.205

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.