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A Global Characterization and Identification of Multifunctional Enzymes
Multi-functional enzymes are enzymes that perform multiple physiological functions. Characterization and identification of multi-functional enzymes are critical for communication and cooperation between different functions and pathways within a complex cellular system or between cells. In present st...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377604/ https://www.ncbi.nlm.nih.gov/pubmed/22723914 http://dx.doi.org/10.1371/journal.pone.0038979 |
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author | Cheng, Xian-Ying Huang, Wei-Juan Hu, Shi-Chang Zhang, Hai-Lei Wang, Hao Zhang, Jing-Xian Lin, Hong-Huang Chen, Yu-Zong Zou, Quan Ji, Zhi-Liang |
author_facet | Cheng, Xian-Ying Huang, Wei-Juan Hu, Shi-Chang Zhang, Hai-Lei Wang, Hao Zhang, Jing-Xian Lin, Hong-Huang Chen, Yu-Zong Zou, Quan Ji, Zhi-Liang |
author_sort | Cheng, Xian-Ying |
collection | PubMed |
description | Multi-functional enzymes are enzymes that perform multiple physiological functions. Characterization and identification of multi-functional enzymes are critical for communication and cooperation between different functions and pathways within a complex cellular system or between cells. In present study, we collected literature-reported 6,799 multi-functional enzymes and systematically characterized them in structural, functional, and evolutionary aspects. It was found that four physiochemical properties, that is, charge, polarizability, hydrophobicity, and solvent accessibility, are important for characterization of multi-functional enzymes. Accordingly, a combinational model of support vector machine and random forest model was constructed, based on which 6,956 potential novel multi-functional enzymes were successfully identified from the ENZYME database. Moreover, it was observed that multi-functional enzymes are non-evenly distributed in species, and that Bacteria have relatively more multi-functional enzymes than Archaebacteria and Eukaryota. Comparative analysis indicated that the multi-functional enzymes experienced a fluctuation of gene gain and loss during the evolution from S. cerevisiae to H. sapiens. Further pathway analyses indicated that a majority of multi-functional enzymes were well preserved in catalyzing several essential cellular processes, for example, metabolisms of carbohydrates, nucleotides, and amino acids. What’s more, a database of known multi-functional enzymes and a server for novel multi-functional enzyme prediction were also constructed for free access at http://bioinf.xmu.edu.cn/databases/MFEs/index.htm. |
format | Online Article Text |
id | pubmed-3377604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33776042012-06-21 A Global Characterization and Identification of Multifunctional Enzymes Cheng, Xian-Ying Huang, Wei-Juan Hu, Shi-Chang Zhang, Hai-Lei Wang, Hao Zhang, Jing-Xian Lin, Hong-Huang Chen, Yu-Zong Zou, Quan Ji, Zhi-Liang PLoS One Research Article Multi-functional enzymes are enzymes that perform multiple physiological functions. Characterization and identification of multi-functional enzymes are critical for communication and cooperation between different functions and pathways within a complex cellular system or between cells. In present study, we collected literature-reported 6,799 multi-functional enzymes and systematically characterized them in structural, functional, and evolutionary aspects. It was found that four physiochemical properties, that is, charge, polarizability, hydrophobicity, and solvent accessibility, are important for characterization of multi-functional enzymes. Accordingly, a combinational model of support vector machine and random forest model was constructed, based on which 6,956 potential novel multi-functional enzymes were successfully identified from the ENZYME database. Moreover, it was observed that multi-functional enzymes are non-evenly distributed in species, and that Bacteria have relatively more multi-functional enzymes than Archaebacteria and Eukaryota. Comparative analysis indicated that the multi-functional enzymes experienced a fluctuation of gene gain and loss during the evolution from S. cerevisiae to H. sapiens. Further pathway analyses indicated that a majority of multi-functional enzymes were well preserved in catalyzing several essential cellular processes, for example, metabolisms of carbohydrates, nucleotides, and amino acids. What’s more, a database of known multi-functional enzymes and a server for novel multi-functional enzyme prediction were also constructed for free access at http://bioinf.xmu.edu.cn/databases/MFEs/index.htm. Public Library of Science 2012-06-18 /pmc/articles/PMC3377604/ /pubmed/22723914 http://dx.doi.org/10.1371/journal.pone.0038979 Text en Cheng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Cheng, Xian-Ying Huang, Wei-Juan Hu, Shi-Chang Zhang, Hai-Lei Wang, Hao Zhang, Jing-Xian Lin, Hong-Huang Chen, Yu-Zong Zou, Quan Ji, Zhi-Liang A Global Characterization and Identification of Multifunctional Enzymes |
title | A Global Characterization and Identification of Multifunctional Enzymes |
title_full | A Global Characterization and Identification of Multifunctional Enzymes |
title_fullStr | A Global Characterization and Identification of Multifunctional Enzymes |
title_full_unstemmed | A Global Characterization and Identification of Multifunctional Enzymes |
title_short | A Global Characterization and Identification of Multifunctional Enzymes |
title_sort | global characterization and identification of multifunctional enzymes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377604/ https://www.ncbi.nlm.nih.gov/pubmed/22723914 http://dx.doi.org/10.1371/journal.pone.0038979 |
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