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The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis

The use of halogen bond is widespread in drug discovery, design, and clinical trials, but is overlooked in drug biosynthesis. Here, the role of halogen bond in the nitrilase-catalyzed synthesis of ortho-, meta-, and para-chlorophenylacetic acid was investigated. Different distributions of halogen bo...

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Detalles Bibliográficos
Autores principales: Jiang, Shuiqin, Zhang, Lujia, Cui, Dongbin, Yao, Zhiqiang, Gao, Bei, Lin, Jinping, Wei, Dongzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052520/
https://www.ncbi.nlm.nih.gov/pubmed/27708371
http://dx.doi.org/10.1038/srep34750
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author Jiang, Shuiqin
Zhang, Lujia
Cui, Dongbin
Yao, Zhiqiang
Gao, Bei
Lin, Jinping
Wei, Dongzhi
author_facet Jiang, Shuiqin
Zhang, Lujia
Cui, Dongbin
Yao, Zhiqiang
Gao, Bei
Lin, Jinping
Wei, Dongzhi
author_sort Jiang, Shuiqin
collection PubMed
description The use of halogen bond is widespread in drug discovery, design, and clinical trials, but is overlooked in drug biosynthesis. Here, the role of halogen bond in the nitrilase-catalyzed synthesis of ortho-, meta-, and para-chlorophenylacetic acid was investigated. Different distributions of halogen bond induced changes of substrate binding conformation and affected substrate selectivity. By engineering the halogen interaction, the substrate selectivity of the enzyme changed, with the implication that halogen bond plays an important role in biosynthesis and should be used as an efficient and reliable tool in enzymatic drug synthesis.
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spelling pubmed-50525202016-10-19 The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis Jiang, Shuiqin Zhang, Lujia Cui, Dongbin Yao, Zhiqiang Gao, Bei Lin, Jinping Wei, Dongzhi Sci Rep Article The use of halogen bond is widespread in drug discovery, design, and clinical trials, but is overlooked in drug biosynthesis. Here, the role of halogen bond in the nitrilase-catalyzed synthesis of ortho-, meta-, and para-chlorophenylacetic acid was investigated. Different distributions of halogen bond induced changes of substrate binding conformation and affected substrate selectivity. By engineering the halogen interaction, the substrate selectivity of the enzyme changed, with the implication that halogen bond plays an important role in biosynthesis and should be used as an efficient and reliable tool in enzymatic drug synthesis. Nature Publishing Group 2016-10-06 /pmc/articles/PMC5052520/ /pubmed/27708371 http://dx.doi.org/10.1038/srep34750 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Jiang, Shuiqin
Zhang, Lujia
Cui, Dongbin
Yao, Zhiqiang
Gao, Bei
Lin, Jinping
Wei, Dongzhi
The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title_full The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title_fullStr The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title_full_unstemmed The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title_short The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis
title_sort important role of halogen bond in substrate selectivity of enzymatic catalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052520/
https://www.ncbi.nlm.nih.gov/pubmed/27708371
http://dx.doi.org/10.1038/srep34750
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