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Symmetry breaking by enzyme-catalyzed epoxide hydrolysis
Janfalk Carlsson et al. [IUCrJ (2018), 5, 269–282] describe studies on factors determining selective ring opening of methylstyrene oxide stereoisomers by the epoxide hydrolase StEH1. The stereo-differentiating step is selective hydrolysis of an alkylated intermediate formed by reaction of the epoxid...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038963/ https://www.ncbi.nlm.nih.gov/pubmed/30002837 http://dx.doi.org/10.1107/S2052252518007005 |
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author | Schofield, Christopher J. |
author_facet | Schofield, Christopher J. |
author_sort | Schofield, Christopher J. |
collection | PubMed |
description | Janfalk Carlsson et al. [IUCrJ (2018), 5, 269–282] describe studies on factors determining selective ring opening of methylstyrene oxide stereoisomers by the epoxide hydrolase StEH1. The stereo-differentiating step is selective hydrolysis of an alkylated intermediate formed by reaction of the epoxide with an aspartyl residue. |
format | Online Article Text |
id | pubmed-6038963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-60389632018-07-12 Symmetry breaking by enzyme-catalyzed epoxide hydrolysis Schofield, Christopher J. IUCrJ Scientific Commentaries Janfalk Carlsson et al. [IUCrJ (2018), 5, 269–282] describe studies on factors determining selective ring opening of methylstyrene oxide stereoisomers by the epoxide hydrolase StEH1. The stereo-differentiating step is selective hydrolysis of an alkylated intermediate formed by reaction of the epoxide with an aspartyl residue. International Union of Crystallography 2018-05-18 /pmc/articles/PMC6038963/ /pubmed/30002837 http://dx.doi.org/10.1107/S2052252518007005 Text en © Christopher J. Schofield 2018 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/ |
spellingShingle | Scientific Commentaries Schofield, Christopher J. Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title | Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title_full | Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title_fullStr | Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title_full_unstemmed | Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title_short | Symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
title_sort | symmetry breaking by enzyme-catalyzed epoxide hydrolysis |
topic | Scientific Commentaries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038963/ https://www.ncbi.nlm.nih.gov/pubmed/30002837 http://dx.doi.org/10.1107/S2052252518007005 |
work_keys_str_mv | AT schofieldchristopherj symmetrybreakingbyenzymecatalyzedepoxidehydrolysis |