4.4 Article

Gneg-mPLoc: A top-down strategy to enhance the quality of predicting subcellular localization of Gram-negative bacterial proteins

期刊

JOURNAL OF THEORETICAL BIOLOGY
卷 264, 期 2, 页码 326-333

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jtbi.2010.01.018

关键词

Multiplex protein; Homology search; Representative proteins; Gene ontology; Functional domain; Sequential evolution; Ensemble classifier; Fusion approach

资金

  1. National Natural Science Foundation of China [60704047]
  2. Science and Technology Commission of Shanghai Municipality [08ZR1410600, 08JC1410600]
  3. Shanghai Municipal Education Commission [10ZZ17]

向作者/读者索取更多资源

By incorporating the information of gene ontology, functional domain, and sequential evolution, a new predictor called Gneg-mPLoc was developed. It can be used to identify Gram-negative bacterial proteins among the following eight locations: (1) cytoplasm, (2) extracellular, (3) fimbrium, (4) flagellum, (5) inner membrane, (6) nucleoid, (7) outer membrane, and (8) periplasm. It can also be used to deal with the case when a query protein may simultaneously exist in more than one location. Compared with the original predictor called Gneg-PLoc, the new predictor is much more powerful and flexible. For a newly constructed stringent benchmark dataset in which none of proteins included has >= 25% pairwise sequence identity to any other in a same subset (location), the overall jackknife success rate achieved by Gneg-mPLoc was 85.5%, which was more than 14% higher than the corresponding rate by the Gneg-PLoc. As a user friendly web-server, Gneg-mPLoc is freely accessible at http://www.csbio.sjtu.edu.cn/bioinf/Gneg-multi/. (C) 2010 Elsevier Ltd. All rights reserved.

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