Computational Protocol for Screening GPI-anchored Proteins

被引:0
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作者
Cao, Wei [1 ]
Sumikoshi, Kazuya [1 ]
Terada, Tohru [2 ]
Nakamura, Shugo [1 ]
Kitamoto, Katsuhiko [1 ]
Shimizu, Kentaro [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Biotechnol, Bunkyo Ku, 1-1-1 Yayoi, Tokyo 1138657, Japan
[2] Univ Tokyo, Grad sch Agr & Life Sci, profess Programme Agr bioinformat, Tokyo, Japan
关键词
GPI-anchored Proteins; SVM; Post-translational modification; SACCHAROMYCES-CEREVISIAE; MODIFICATION SITES; SIGNAL PEPTIDES; GENOME-WIDE; MEMBRANE; PREDICTION; IDENTIFICATION; LOCALIZATION; ATTACHMENT; SCRAPIE;
D O I
暂无
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Glycosylphosphatidylinositol (GPI) lipid modification is an important protein posttranslational modification found in many organisms, and GPI-anchoring is confined to the C-terminus of the target protein. We have developed a novel computational protocol for identifying GPI-anchored proteins, which is more accurate than previously proposed protocols. It uses an optimized support vector machine (SVM) classifier to recognize the C-terminal sequence pattern and uses a voting system based on SignalP version 3.0 to determine the presence or absence of the N-terminal signal of a typical GPI-anchored protein. The SVM classifier shows an accuracy of 96%, and the area under the receiver operating characteristic (ROC) curve is 0.97 under a 5-fold cross-validation test. Fourteen of 15 proteins in our sensitivity test dataset and 19 of the 20 proteins experimentally identified by Hamada et al. that were not included in the training dataset were identified correctly. This suggests that our protocol is considerably effective on unseen data. A proteome-wide survey applying the protocol to S. cerevisiae identified 88 proteins as putative GPI-anchored proteins.
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页码:164 / +
页数:3
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