GRID/tetrahedral intermediate computational approach to the study of selectivity of penicillin G acylase in amide bond synthesis
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics,Analytical Chemistry
Reference27 articles.
1. Enhancement of the enantioselectivity of penicillin G acylase from E. coli by “substrate tuning”
2. The use of immobilized penicillin G acylase in organic synthesis;Baldaro,1992
3. Enantioselective acylation of a beta-lactam intermediate in the synthesis of loracarbef using penicillin G amidase
4. High isolated yields in thermodynamically controlled peptide synthesis in toluene catalysed by thermolysin adsorbed on Celite R-640
5. d-Phenylglycine and d-4-hydroxyphenylglycine methyl esters via penicillin G acylase catalysed resolution in organic solvents
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1. In-silico driven engineering of enantioselectivity of a penicillin G acylase towards active pharmaceutical ingredients;Journal of Molecular Catalysis B: Enzymatic;2016-11
2. Catalytic Cycle of Penicillin Acylase from Escherichia coli: QM/MM Modeling of Chemical Transformations in the Enzyme Active Site upon Penicillin G Hydrolysis;ACS Catalysis;2014-06-30
3. Perspectives and industrial potential of PGA selectivity and promiscuity;Biotechnology Advances;2013-12
4. Reactivation of penicillin acylase biocatalysts: Effect of the intensity of enzyme–support attachment and enzyme load;Journal of Molecular Catalysis B: Enzymatic;2012-02
5. In Silico Analysis of Enzyme Surface and Glycosylation Effect as a Tool for Efficient Covalent Immobilisation of CalB and PGA on Sepabeads®;Advanced Synthesis & Catalysis;2007-04-02
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