Parallel Computations in the Development of Thermostable Lipase Mutants
- Авторы: Kondratyev M.S.1, Kabanov A.V.1, Samchenko A.A.1, Komarov V.M.1, Khechinashvili N.N.1
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Учреждения:
- Institute of Cell Biophysics
- Выпуск: Том 59, № 8 (2018)
- Страницы: 1974-1979
- Раздел: Article
- URL: https://journals.rcsi.science/0022-4766/article/view/161819
- DOI: https://doi.org/10.1134/S0022476618080292
- ID: 161819
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Аннотация
The advanced high performance computing methods are used to study the stability and conformational dynamics of the bacterial enzyme lipase LipA, its mutants, and the close homologous enzyme CLE whose substrate is polylactic acid-based plastics. From the analysis of the GPU molecular dynamics of native lipases and their mutants the amino acid residues whose point substitutions can markedly improve the thermostability of the enzymes under study without deteriorating their activity are determined.
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Об авторах
M. Kondratyev
Institute of Cell Biophysics
Автор, ответственный за переписку.
Email: ma-ko@bk.ru
Россия, Pushchino
A. Kabanov
Institute of Cell Biophysics
Email: ma-ko@bk.ru
Россия, Pushchino
A. Samchenko
Institute of Cell Biophysics
Email: ma-ko@bk.ru
Россия, Pushchino
V. Komarov
Institute of Cell Biophysics
Email: ma-ko@bk.ru
Россия, Pushchino
N. Khechinashvili
Institute of Cell Biophysics
Email: ma-ko@bk.ru
Россия, Pushchino
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