WEKO3
アイテム
Support Vector Machine Prediction of N- and O-glycosylation Sites Using Whole Sequence Information and Subcellular Localization
https://ipsj.ixsq.nii.ac.jp/records/60787
https://ipsj.ixsq.nii.ac.jp/records/60787a5cfe48d-25c3-41f9-baed-4c7974414b66
名前 / ファイル | ライセンス | アクション |
---|---|---|
![]() |
Copyright (c) 2009 by the Information Processing Society of Japan
|
|
オープンアクセス |
Item type | Trans(1) | |||||||
---|---|---|---|---|---|---|---|---|
公開日 | 2009-03-24 | |||||||
タイトル | ||||||||
タイトル | Support Vector Machine Prediction of N- and O-glycosylation Sites Using Whole Sequence Information and Subcellular Localization | |||||||
タイトル | ||||||||
言語 | en | |||||||
タイトル | Support Vector Machine Prediction of N- and O-glycosylation Sites Using Whole Sequence Information and Subcellular Localization | |||||||
言語 | ||||||||
言語 | eng | |||||||
キーワード | ||||||||
主題Scheme | Other | |||||||
主題 | Original Papers | |||||||
資源タイプ | ||||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||||
資源タイプ | journal article | |||||||
著者所属 | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者所属 | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者所属 | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者所属(英) | ||||||||
en | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者所属(英) | ||||||||
en | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者所属(英) | ||||||||
en | ||||||||
Department of Biosciences and Informatics, Keio University | ||||||||
著者名 |
Kenta, Sasaki
× Kenta, Sasaki
|
|||||||
著者名(英) |
Kenta, Sasaki
× Kenta, Sasaki
|
|||||||
論文抄録 | ||||||||
内容記述タイプ | Other | |||||||
内容記述 | Background: Glycans, or sugar chains, are one of the three types of chain (DNA, protein and glycan) that constitute living organisms; they are often called "the third chain of the living organism". About half of all proteins are estimated to be glycosylated based on the SWISS-PROT database. Glycosylation is one of the most important post-translational modifications, affecting many critical functions of proteins, including cellular communication, and their tertiary structure. In order to computationally predict N-glycosylation and Oglycosylation sites, we developed three kinds of support vector machine (SVM) model, which utilize local information, general protein information and/or subcellular localization in consideration of the binding specificity of glycosyltransferases and the characteristic subcellular localization of glycoproteins. Results: In our computational experiment, the model integrating three kinds of information achieved about 90% accuracy in predictions of both N-glycosylation and O-glycosylation sites. Moreover, our model was applied to a protein whose glycosylation sites had not been previously identified and we succeeded in showing that the glycosylation sites predicted by our model were structurally reasonable. Conclusions: In the present study, we developed a comprehensive and effective computational method that detects glycosylation sites. We conclude that our method is a comprehensive and effective computational prediction method that is applicable at a genome-wide level. | |||||||
論文抄録(英) | ||||||||
内容記述タイプ | Other | |||||||
内容記述 | Background: Glycans, or sugar chains, are one of the three types of chain (DNA, protein and glycan) that constitute living organisms; they are often called "the third chain of the living organism". About half of all proteins are estimated to be glycosylated based on the SWISS-PROT database. Glycosylation is one of the most important post-translational modifications, affecting many critical functions of proteins, including cellular communication, and their tertiary structure. In order to computationally predict N-glycosylation and Oglycosylation sites, we developed three kinds of support vector machine (SVM) model, which utilize local information, general protein information and/or subcellular localization in consideration of the binding specificity of glycosyltransferases and the characteristic subcellular localization of glycoproteins. Results: In our computational experiment, the model integrating three kinds of information achieved about 90% accuracy in predictions of both N-glycosylation and O-glycosylation sites. Moreover, our model was applied to a protein whose glycosylation sites had not been previously identified and we succeeded in showing that the glycosylation sites predicted by our model were structurally reasonable. Conclusions: In the present study, we developed a comprehensive and effective computational method that detects glycosylation sites. We conclude that our method is a comprehensive and effective computational prediction method that is applicable at a genome-wide level. | |||||||
書誌レコードID | ||||||||
収録物識別子タイプ | NCID | |||||||
収録物識別子 | AA12177013 | |||||||
書誌情報 |
IPSJ Transactions on Bioinformatics (TBIO) 巻 2, p. 25-35, 発行日 2009-03-24 |
|||||||
ISSN | ||||||||
収録物識別子タイプ | ISSN | |||||||
収録物識別子 | 1882-6679 | |||||||
出版者 | ||||||||
言語 | ja | |||||||
出版者 | 情報処理学会 |