Open Access Highly Accessed Research article

Protein network prediction and topological analysis in Leishmania major as a tool for drug target selection

Andrés F Flórez1, Daeui Park2, Jong Bhak2, Byoung-Chul Kim2, Allan Kuchinsky3, John H Morris4, Jairo Espinosa5 and Carlos Muskus1*

1 Programa de Estudio y Control de Enfermedades Tropicales-PECET, Universidad de Antioquia, Calle 62 No 52-59, Lab. 632, Medellín, Colombia

2 Korean BioInformation Center (KOBIC), KRIBB, Daejeon, 305-806, Korea

3 Agilent Technologies, Santa Clara, California, USA

4 Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, USA

5 Grupo de Automática-GAUNAL, Universidad Nacional Sede Medellín, Medellín, Colombia

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BMC Bioinformatics 2010, 11:484 doi:10.1186/1471-2105-11-484

Published: 27 September 2010

Additional files

Additional file 1:

Cytoscape network of Leishmania interactome. Leishmania major interactome in Cytoscape format with the annotation and topological metrics as Cytoscape attributes.

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Additional file 2:

Table S1: List of targets detected by connectivity and betweenness centrality but not filtered for human homology.

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Additional file 3:

Table S2: Final list of targets, excluding those with human orthologs from table S1.

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Additional file 4:

Table S3: Clusters IDs from the whole network with overrepresented GO codes and p-values.

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Additional file 5:

Table S4: List of hypothetical proteins with predicted biological process derived from the clustering and enrichment analysis.

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Additional file 6:

Table S5: Number of essential genes for each GO Biological process.

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