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Anatomy of enzyme channels
BACKGROUND: Enzyme active sites can be connected to the exterior environment by one or more channels passing through the protein. Despite our current knowledge of enzyme structure and function, surprisingly little is known about how often channels are present or about any structural features such ch...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245731/ https://www.ncbi.nlm.nih.gov/pubmed/25403510 http://dx.doi.org/10.1186/s12859-014-0379-x |
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author | Pravda, Lukáš Berka, Karel Svobodová Vařeková, Radka Sehnal, David Banáš, Pavel Laskowski, Roman A Koča, Jaroslav Otyepka, Michal |
author_facet | Pravda, Lukáš Berka, Karel Svobodová Vařeková, Radka Sehnal, David Banáš, Pavel Laskowski, Roman A Koča, Jaroslav Otyepka, Michal |
author_sort | Pravda, Lukáš |
collection | PubMed |
description | BACKGROUND: Enzyme active sites can be connected to the exterior environment by one or more channels passing through the protein. Despite our current knowledge of enzyme structure and function, surprisingly little is known about how often channels are present or about any structural features such channels may have in common. RESULTS: Here, we analyze the long channels (i.e. >15 Å) leading to the active sites of 4,306 enzyme structures. We find that over 64% of enzymes contain two or more long channels, their typical length being 28 Å. We show that amino acid compositions of the channel significantly differ both to the composition of the active site, surface and interior of the protein. CONCLUSIONS: The majority of enzymes have buried active sites accessible via a network of access channels. This indicates that enzymes tend to have buried active sites, with channels controlling access to, and egress from, them, and that suggests channels may play a key role in helping determine enzyme substrate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0379-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4245731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42457312014-11-28 Anatomy of enzyme channels Pravda, Lukáš Berka, Karel Svobodová Vařeková, Radka Sehnal, David Banáš, Pavel Laskowski, Roman A Koča, Jaroslav Otyepka, Michal BMC Bioinformatics Research Article BACKGROUND: Enzyme active sites can be connected to the exterior environment by one or more channels passing through the protein. Despite our current knowledge of enzyme structure and function, surprisingly little is known about how often channels are present or about any structural features such channels may have in common. RESULTS: Here, we analyze the long channels (i.e. >15 Å) leading to the active sites of 4,306 enzyme structures. We find that over 64% of enzymes contain two or more long channels, their typical length being 28 Å. We show that amino acid compositions of the channel significantly differ both to the composition of the active site, surface and interior of the protein. CONCLUSIONS: The majority of enzymes have buried active sites accessible via a network of access channels. This indicates that enzymes tend to have buried active sites, with channels controlling access to, and egress from, them, and that suggests channels may play a key role in helping determine enzyme substrate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0379-x) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-18 /pmc/articles/PMC4245731/ /pubmed/25403510 http://dx.doi.org/10.1186/s12859-014-0379-x Text en © Pravda et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pravda, Lukáš Berka, Karel Svobodová Vařeková, Radka Sehnal, David Banáš, Pavel Laskowski, Roman A Koča, Jaroslav Otyepka, Michal Anatomy of enzyme channels |
title | Anatomy of enzyme channels |
title_full | Anatomy of enzyme channels |
title_fullStr | Anatomy of enzyme channels |
title_full_unstemmed | Anatomy of enzyme channels |
title_short | Anatomy of enzyme channels |
title_sort | anatomy of enzyme channels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245731/ https://www.ncbi.nlm.nih.gov/pubmed/25403510 http://dx.doi.org/10.1186/s12859-014-0379-x |
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