Virtual Screening of Thiol Peroxiredoxin 6 Reducers
- Autores: Kondratyev M.S.1, Zakharova E.V.1,2
-
Afiliações:
- Institute of Cell Biophysics, Russian Academy of Sciences
- Moscow State University
- Edição: Volume 63, Nº 5 (2018)
- Páginas: 669-674
- Seção: Molecular Biophysics
- URL: https://ogarev-online.ru/0006-3509/article/view/152705
- DOI: https://doi.org/10.1134/S0006350918050123
- ID: 152705
Citar
Resumo
Abstract—Virtual screening of possible thiol reducers for peroxiredoxin 6, which is one of the most important components of the antioxidant system in a number of living organisms, including humans, was performed. The mechanism of functioning of this protein was studied earlier; however, the search for new reducing agents and their study is still important. According to our hypothesis short cysteine-containing peptides, as well as small thiol compounds, can serve as reducing agents. In the present study, interactions of peroxiredoxin 6 with captopril, unithiol, succimer, cystamine, and three cystein-containing peptides, ECECE, KCKCK, and CCCCC, were simulated and analyzed. The most promising molecules for further study were revealed by the methods of molecular modeling and docking. A new atypical binding site for thiol ligands was found on the surface of the peroxiredoxin 6 molecule.
Palavras-chave
Sobre autores
M. Kondratyev
Institute of Cell Biophysics, Russian Academy of Sciences
Autor responsável pela correspondência
Email: ma-ko@bk.ru
Rússia, Pushchino, Moscow oblast, 142290
E. Zakharova
Institute of Cell Biophysics, Russian Academy of Sciences; Moscow State University
Email: ma-ko@bk.ru
Rússia, Pushchino, Moscow oblast, 142290; Moscow, 119991
Arquivos suplementares
