Parallel Computations in the Development of Thermostable Lipase Mutants
- 作者: Kondratyev M.S.1, Kabanov A.V.1, Samchenko A.A.1, Komarov V.M.1, Khechinashvili N.N.1
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隶属关系:
- Institute of Cell Biophysics
- 期: 卷 59, 编号 8 (2018)
- 页面: 1974-1979
- 栏目: Article
- URL: https://bakhtiniada.ru/0022-4766/article/view/161819
- DOI: https://doi.org/10.1134/S0022476618080292
- ID: 161819
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详细
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.
作者简介
M. Kondratyev
Institute of Cell Biophysics
编辑信件的主要联系方式.
Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino
A. Kabanov
Institute of Cell Biophysics
Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino
A. Samchenko
Institute of Cell Biophysics
Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino
V. Komarov
Institute of Cell Biophysics
Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino
N. Khechinashvili
Institute of Cell Biophysics
Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino
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