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SSER: Species specific essential reactions database

BACKGROUND: Essential reactions are vital components of cellular networks. They are the foundations of synthetic biology and are potential candidate targets for antimetabolic drug design. Especially if a single reaction is catalyzed by multiple enzymes, then inhibiting the reaction would be a better...

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Autores principales: Labena, Abraham A., Ye, Yuan-Nong, Dong, Chuan, Zhang, Fa-Z, Guo, Feng-Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395902/
https://www.ncbi.nlm.nih.gov/pubmed/28420402
http://dx.doi.org/10.1186/s12918-017-0426-0
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author Labena, Abraham A.
Ye, Yuan-Nong
Dong, Chuan
Zhang, Fa-Z
Guo, Feng-Biao
author_facet Labena, Abraham A.
Ye, Yuan-Nong
Dong, Chuan
Zhang, Fa-Z
Guo, Feng-Biao
author_sort Labena, Abraham A.
collection PubMed
description BACKGROUND: Essential reactions are vital components of cellular networks. They are the foundations of synthetic biology and are potential candidate targets for antimetabolic drug design. Especially if a single reaction is catalyzed by multiple enzymes, then inhibiting the reaction would be a better option than targeting the enzymes or the corresponding enzyme-encoding gene. The existing databases such as BRENDA, BiGG, KEGG, Bio-models, Biosilico, and many others offer useful and comprehensive information on biochemical reactions. But none of these databases especially focus on essential reactions. Therefore, building a centralized repository for this class of reactions would be of great value. DESCRIPTION: Here, we present a species-specific essential reactions database (SSER). The current version comprises essential biochemical and transport reactions of twenty-six organisms which are identified via flux balance analysis (FBA) combined with manual curation on experimentally validated metabolic network models. Quantitative data on the number of essential reactions, number of the essential reactions associated with their respective enzyme-encoding genes and shared essential reactions across organisms are the main contents of the database. CONCLUSION: SSER would be a prime source to obtain essential reactions data and related gene and metabolite information and it can significantly facilitate the metabolic network models reconstruction and analysis, and drug target discovery studies. Users can browse, search, compare and download the essential reactions of organisms of their interest through the website http://cefg.uestc.edu.cn/sser. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0426-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-53959022017-04-20 SSER: Species specific essential reactions database Labena, Abraham A. Ye, Yuan-Nong Dong, Chuan Zhang, Fa-Z Guo, Feng-Biao BMC Syst Biol Database BACKGROUND: Essential reactions are vital components of cellular networks. They are the foundations of synthetic biology and are potential candidate targets for antimetabolic drug design. Especially if a single reaction is catalyzed by multiple enzymes, then inhibiting the reaction would be a better option than targeting the enzymes or the corresponding enzyme-encoding gene. The existing databases such as BRENDA, BiGG, KEGG, Bio-models, Biosilico, and many others offer useful and comprehensive information on biochemical reactions. But none of these databases especially focus on essential reactions. Therefore, building a centralized repository for this class of reactions would be of great value. DESCRIPTION: Here, we present a species-specific essential reactions database (SSER). The current version comprises essential biochemical and transport reactions of twenty-six organisms which are identified via flux balance analysis (FBA) combined with manual curation on experimentally validated metabolic network models. Quantitative data on the number of essential reactions, number of the essential reactions associated with their respective enzyme-encoding genes and shared essential reactions across organisms are the main contents of the database. CONCLUSION: SSER would be a prime source to obtain essential reactions data and related gene and metabolite information and it can significantly facilitate the metabolic network models reconstruction and analysis, and drug target discovery studies. Users can browse, search, compare and download the essential reactions of organisms of their interest through the website http://cefg.uestc.edu.cn/sser. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0426-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-19 /pmc/articles/PMC5395902/ /pubmed/28420402 http://dx.doi.org/10.1186/s12918-017-0426-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Database
Labena, Abraham A.
Ye, Yuan-Nong
Dong, Chuan
Zhang, Fa-Z
Guo, Feng-Biao
SSER: Species specific essential reactions database
title SSER: Species specific essential reactions database
title_full SSER: Species specific essential reactions database
title_fullStr SSER: Species specific essential reactions database
title_full_unstemmed SSER: Species specific essential reactions database
title_short SSER: Species specific essential reactions database
title_sort sser: species specific essential reactions database
topic Database
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395902/
https://www.ncbi.nlm.nih.gov/pubmed/28420402
http://dx.doi.org/10.1186/s12918-017-0426-0
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