Atropselective Hydrolysis of Chiral Binol-Phosphate Esters Catalyzed by the Phosphotriesterase from Sphingobium sp. TCM1
Author:
Affiliation:
1. Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States
Funder
National Institute of General Medical Sciences
Robert A Welch Foundation
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.0c00831
Reference17 articles.
1. Structural Determinants for the Stereoselective Hydrolysis of Chiral Substrates by Phosphotriesterase
2. Stereoselective Hydrolysis of Organophosphate Nerve Agents by the Bacterial Phosphotriesterase
3. Multiple Reaction Products from the Hydrolysis of Chiral and Prochiral Organophosphate Substrates by the Phosphotriesterase from Sphingobium sp. TCM1
4. Stereoselective Formation of Multiple Reaction Products by the Phosphotriesterase from Sphingobium sp. TCM1
5. Transition State Analysis of the Reaction Catalyzed by the Phosphotriesterase from Sphingobium sp. TCM1
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1. QM/MM and MM MD Simulations on Enzymatic Degradation of the Nerve Agent VR by Phosphotriesterase;The Journal of Physical Chemistry B;2023-08-16
2. Degradation of pesticides diazinon and diazoxon by phosphotriesterase: insight into divergent mechanisms from QM/MM and MD simulations;Physical Chemistry Chemical Physics;2022
3. QM/MM and MM MD simulations on decontamination of the V-type nerve agent VX by phosphotriesterase: toward a comprehensive understanding of steroselectivity and activity;Physical Chemistry Chemical Physics;2022
4. Stereoisomer-Independent Stable Blue Emission in Axial Chiral Difluorenol;Frontiers in Chemistry;2021-09-03
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