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Insights into enzymatic halogenation from computational studies
The halogenases are a group of enzymes that have only come to the fore over the last 10 years thanks to the discovery and characterization of several novel representatives. They have revealed the fascinating variety of distinct chemical mechanisms that nature utilizes to activate halogens and introd...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227530/ https://www.ncbi.nlm.nih.gov/pubmed/25426489 http://dx.doi.org/10.3389/fchem.2014.00098 |
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author | Senn, Hans M. |
author_facet | Senn, Hans M. |
author_sort | Senn, Hans M. |
collection | PubMed |
description | The halogenases are a group of enzymes that have only come to the fore over the last 10 years thanks to the discovery and characterization of several novel representatives. They have revealed the fascinating variety of distinct chemical mechanisms that nature utilizes to activate halogens and introduce them into organic substrates. Computational studies using a range of approaches have already elucidated many details of the mechanisms of these enzymes, often in synergistic combination with experiment. This Review summarizes the main insights gained from these studies. It also seeks to identify open questions that are amenable to computational investigations. The studies discussed herein serve to illustrate some of the limitations of the current computational approaches and the challenges encountered in computational mechanistic enzymology. |
format | Online Article Text |
id | pubmed-4227530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42275302014-11-25 Insights into enzymatic halogenation from computational studies Senn, Hans M. Front Chem Chemistry The halogenases are a group of enzymes that have only come to the fore over the last 10 years thanks to the discovery and characterization of several novel representatives. They have revealed the fascinating variety of distinct chemical mechanisms that nature utilizes to activate halogens and introduce them into organic substrates. Computational studies using a range of approaches have already elucidated many details of the mechanisms of these enzymes, often in synergistic combination with experiment. This Review summarizes the main insights gained from these studies. It also seeks to identify open questions that are amenable to computational investigations. The studies discussed herein serve to illustrate some of the limitations of the current computational approaches and the challenges encountered in computational mechanistic enzymology. Frontiers Media S.A. 2014-11-11 /pmc/articles/PMC4227530/ /pubmed/25426489 http://dx.doi.org/10.3389/fchem.2014.00098 Text en Copyright © 2014 Senn. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Senn, Hans M. Insights into enzymatic halogenation from computational studies |
title | Insights into enzymatic halogenation from computational studies |
title_full | Insights into enzymatic halogenation from computational studies |
title_fullStr | Insights into enzymatic halogenation from computational studies |
title_full_unstemmed | Insights into enzymatic halogenation from computational studies |
title_short | Insights into enzymatic halogenation from computational studies |
title_sort | insights into enzymatic halogenation from computational studies |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227530/ https://www.ncbi.nlm.nih.gov/pubmed/25426489 http://dx.doi.org/10.3389/fchem.2014.00098 |
work_keys_str_mv | AT sennhansm insightsintoenzymatichalogenationfromcomputationalstudies |