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Prediction of S-nitrosylation sites by integrating support vector machines and random forest

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dc.contributor.authorHasan, MM-
dc.contributor.authorManavalan, B-
dc.contributor.authorKhatun, MS-
dc.contributor.authorKurata, H-
dc.date.accessioned2020-11-17T05:33:01Z-
dc.date.available2020-11-17T05:33:01Z-
dc.date.issued2019-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/19127-
dc.description.abstractCysteine S-nitrosylation is a type of reversible post-translational modification of proteins, which controls diverse biological processes. It is associated with redox-based cellular signaling to protect against oxidative stress. The identification of S-nitrosylation sites is an important step to reveal the function of proteins: however, experimental identification of S-nitrosylation is expensive and time-consuming work. Hence, sequence-based computational prediction of potential S-nitrosylation sites is highly sought before experimentation. Herein, a novel predictor PreSNO has been developed that integrates multiple encoding schemes by the support vector machine and random forest algorithms. The PreSNO achieved an accuracy and Matthews correlation coefficient value of 0.752 and 0.252 respectively in classifying between SNO and non-SNO sites when evaluated on the independent dataset, outperforming the existing methods. The web application of the PreSNO and its associated datasets are freely available at http://kurata14.bio.kyutech.ac.jp/PreSNO/.-
dc.language.isoen-
dc.subject.MESHAlgorithms-
dc.subject.MESHComputational Biology-
dc.subject.MESHCysteine-
dc.subject.MESHProtein Processing, Post-Translational-
dc.subject.MESHSoftware-
dc.subject.MESHSupport Vector Machine-
dc.titlePrediction of S-nitrosylation sites by integrating support vector machines and random forest-
dc.typeArticle-
dc.identifier.pmid31710075-
dc.contributor.affiliatedAuthorBalachandran, Manavalan-
dc.type.localJournal Papers-
dc.identifier.doi10.1039/c9mo00098d-
dc.citation.titleMolecular omics-
dc.citation.volume15-
dc.citation.number6-
dc.citation.date2019-
dc.citation.startPage451-
dc.citation.endPage458-
dc.identifier.bibliographicCitationMolecular omics, 15(6). : 451-458, 2019-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn2515-4184-
dc.relation.journalidJ025154184-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
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