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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/31015
Title: A Unified Proteochemometric Model for Prediction of Inhibition of Cytochrome P450 Isoforms
Authors: Maris Lapins
Apilak Worachartcheewan
Ola Spjuth
Valentin Georgiev
Virapong Prachayasittikul
Chanin Nantasenamat
Jarl E S Wikberg
Uppsala Universitet
Mahidol University
Keywords: Agricultural and Biological Sciences;Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 17-Jun-2013
Citation: PLoS ONE. Vol.8, No.6 (2013)
Abstract: A unified proteochemometric (PCM) model for the prediction of the ability of drug-like chemicals to inhibit five major drug metabolizing CYP isoforms (i.e. CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A4) was created and made publicly available under the Bioclipse Decision Support open source system at www.cyp450model.org. In regards to the proteochemometric modeling we represented the chemical compounds by molecular signature descriptors and the CYP-isoforms by alignment-independent description of composition and transition of amino acid properties of their protein primary sequences. The entire training dataset contained 63 391 interactions and the best PCM model was obtained using signature descriptors of height 1, 2 and 3 and inducing the model with a support vector machine. The model showed excellent predictive ability with internal AUC = 0.923 and an external AUC = 0.940, as evaluated on a large external dataset. The advantage of PCM models is their extensibility making it possible to extend our model for new CYP isoforms and polymorphic CYP forms. A key benefit of PCM is that all proteins are confined in one single model, which makes it generally more stable and predictive as compared with single target models. The inclusion of the model in Bioclipse Decision Support makes it possible to make virtual instantaneous predictions (∼100 ms per prediction) while interactively drawing or modifying chemical structures in the Bioclipse chemical structure editor. © 2013 Lapins et al.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84879169300&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/31015
ISSN: 19326203
Appears in Collections:Scopus 2011-2015

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