Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0038979
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dc.titleA global characterization and identification of multifunctional enzymes
dc.contributor.authorCheng, X.-Y.
dc.contributor.authorHuang, W.-J.
dc.contributor.authorHu, S.-C.
dc.contributor.authorZhang, H.-L.
dc.contributor.authorWang, H.
dc.contributor.authorZhang, J.-X.
dc.contributor.authorLin, H.-H.
dc.contributor.authorChen, Y.-Z.
dc.contributor.authorZou, Q.
dc.contributor.authorJi, Z.-L.
dc.date.accessioned2014-10-29T01:47:22Z
dc.date.available2014-10-29T01:47:22Z
dc.date.issued2012-06-18
dc.identifier.citationCheng, X.-Y., Huang, W.-J., Hu, S.-C., Zhang, H.-L., Wang, H., Zhang, J.-X., Lin, H.-H., Chen, Y.-Z., Zou, Q., Ji, Z.-L. (2012-06-18). A global characterization and identification of multifunctional enzymes. PLoS ONE 7 (6) : -. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0038979
dc.identifier.issn19326203
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/105565
dc.description.abstractMulti-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. © 2012 Cheng et al.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1371/journal.pone.0038979
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1371/journal.pone.0038979
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue6
dc.description.page-
dc.identifier.isiut000305583300076
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