MOTIVATION: Knowing the localization of a protein within the cell helps elucidate its role in biological processes, its function and its potential as a drug target. Thus, subcellular localization prediction is an active research area. Numerous localization prediction systems are described in the literature; some focus on specific localizations or organisms, while others attempt to cover a wide range of localizations. RESULTS: We introduce SherLoc, a new comprehensive system for predicting the localization of eukaryotic proteins. It integrates several types of sequence and text-based features. While applying the widely used support vector machines (SVMs), SherLoc's main novelty lies in the way in which it selects its text sources and features, and integrates those with sequence-based features. We test SherLoc on previously used datasets, as well as on a new set devised specifically to test its predictive power, and show that SherLoc consistently improves on previous reported results. We also report the results of applying SherLoc to a large set of yet-unlocalized proteins. AVAILABILITY: SherLoc, along with Supplementary Information, is available at: http://www-bs.informatik.uni-tuebingen.de/Services/SherLoc/
MOTIVATION: Knowing the localization of a protein within the cell helps elucidate its role in biological processes, its function and its potential as a drug target. Thus, subcellular localization prediction is an active research area. Numerous localization prediction systems are described in the literature; some focus on specific localizations or organisms, while others attempt to cover a wide range of localizations. RESULTS: We introduce SherLoc, a new comprehensive system for predicting the localization of eukaryotic proteins. It integrates several types of sequence and text-based features. While applying the widely used support vector machines (SVMs), SherLoc's main novelty lies in the way in which it selects its text sources and features, and integrates those with sequence-based features. We test SherLoc on previously used datasets, as well as on a new set devised specifically to test its predictive power, and show that SherLoc consistently improves on previous reported results. We also report the results of applying SherLoc to a large set of yet-unlocalized proteins. AVAILABILITY: SherLoc, along with Supplementary Information, is available at: http://www-bs.informatik.uni-tuebingen.de/Services/SherLoc/
Authors: Ishwinder Kaur; Gabriele Schramm; Bart Everts; Thomas Scholzen; Karin B Kindle; Christian Beetz; Cristina Montiel-Duarte; Silke Blindow; Arwyn T Jones; Helmut Haas; Snjezana Stolnik; David M Heery; Franco H Falcone Journal: Infect Immun Date: 2011-01-10 Impact factor: 3.441
Authors: Kishore C S Panigrahi; Madhusmita Panigrahy; Marco Vervliet-Scheebaum; Daniel Lang; Ralf Reski; Man Mohan Johri Journal: Plant Cell Rep Date: 2009-10-02 Impact factor: 4.570
Authors: Kwang-Hyung Kim; Sven D Willger; Sang-Wook Park; Srisombat Puttikamonkul; Nora Grahl; Yangrae Cho; Biswarup Mukhopadhyay; Robert A Cramer; Christopher B Lawrence Journal: PLoS Pathog Date: 2009-11-06 Impact factor: 6.823