Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase

Schistosomiasis is a neglected tropical disease caused by a parasite Schistosoma mansoni and affects over 200 million annually. There is an urgent need to discover novel therapeutic options to control the disease with the recent emergence of drug resistance. The multifunctional protein, thioredoxin...

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Main Authors: Sonam Gaba, Salma Jamal, Open Source Drug Discovery Consortium, Vinod Scaria
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1155/2014/957107
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author Sonam Gaba
Salma Jamal
Open Source Drug Discovery Consortium
Vinod Scaria
author_facet Sonam Gaba
Salma Jamal
Open Source Drug Discovery Consortium
Vinod Scaria
author_sort Sonam Gaba
collection DOAJ
description Schistosomiasis is a neglected tropical disease caused by a parasite Schistosoma mansoni and affects over 200 million annually. There is an urgent need to discover novel therapeutic options to control the disease with the recent emergence of drug resistance. The multifunctional protein, thioredoxin glutathione reductase (TGR), an essential enzyme for the survival of the pathogen in the redox environment has been actively explored as a potential drug target. The recent availability of small-molecule screening datasets against this target provides a unique opportunity to learn molecular properties and apply computational models for discovery of activities in large molecular libraries. Such a prioritisation approach could have the potential to reduce the cost of failures in lead discovery. A supervised learning approach was employed to develop a cost sensitive classification model to evaluate the biological activity of the molecules. Random forest was identified to be the best classifier among all the classifiers with an accuracy of around 80 percent. Independent analysis using a maximally occurring substructure analysis revealed 10 highly enriched scaffolds in the actives dataset and their docking against was also performed. We show that a combined approach of machine learning and other cheminformatics approaches such as substructure comparison and molecular docking is efficient to prioritise molecules from large molecular datasets.
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institution Kabale University
issn 2356-6140
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spelling doaj-art-64e599cfca6041c0961e5422f6ee62872025-08-20T03:34:36ZengWileyThe Scientific World Journal2356-61401537-744X2014-01-01201410.1155/2014/957107957107Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione ReductaseSonam Gaba0Salma Jamal1Open Source Drug Discovery Consortium2Vinod Scaria3GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Mall Road, Delhi 110007, IndiaCSIR Open Source Drug Discovery Unit, Anusandhan Bhawan, 2 Rafi Marg, Delhi 110001, IndiaCSIR Open Source Drug Discovery Unit, Anusandhan Bhawan, 2 Rafi Marg, Delhi 110001, IndiaGN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Mall Road, Delhi 110007, IndiaSchistosomiasis is a neglected tropical disease caused by a parasite Schistosoma mansoni and affects over 200 million annually. There is an urgent need to discover novel therapeutic options to control the disease with the recent emergence of drug resistance. The multifunctional protein, thioredoxin glutathione reductase (TGR), an essential enzyme for the survival of the pathogen in the redox environment has been actively explored as a potential drug target. The recent availability of small-molecule screening datasets against this target provides a unique opportunity to learn molecular properties and apply computational models for discovery of activities in large molecular libraries. Such a prioritisation approach could have the potential to reduce the cost of failures in lead discovery. A supervised learning approach was employed to develop a cost sensitive classification model to evaluate the biological activity of the molecules. Random forest was identified to be the best classifier among all the classifiers with an accuracy of around 80 percent. Independent analysis using a maximally occurring substructure analysis revealed 10 highly enriched scaffolds in the actives dataset and their docking against was also performed. We show that a combined approach of machine learning and other cheminformatics approaches such as substructure comparison and molecular docking is efficient to prioritise molecules from large molecular datasets.http://dx.doi.org/10.1155/2014/957107
spellingShingle Sonam Gaba
Salma Jamal
Open Source Drug Discovery Consortium
Vinod Scaria
Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
The Scientific World Journal
title Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
title_full Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
title_fullStr Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
title_full_unstemmed Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
title_short Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase
title_sort cheminformatics models for inhibitors of schistosoma mansoni thioredoxin glutathione reductase
url http://dx.doi.org/10.1155/2014/957107
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