Heavy path mining of protein-protein associations in the malaria parasite

Methods. 2015 Jul 15:83:63-70. doi: 10.1016/j.ymeth.2015.04.002. Epub 2015 Apr 7.

Abstract

Annotating and understanding the function of proteins and other elements in a genome can be difficult in the absence of a well-studied and evolutionarily close relative. The causative agent of malaria, one of the oldest and most deadly global infectious diseases, is a good example of this problem. The burden of malaria is huge and there is a pressing need for new, more effective antimalarial strategies. However, techniques such as homology-dependent annotation transfer are severely impaired in this parasite because there are no well-understood close relatives. To circumvent this approach we developed a network-based method that uses a heavy path network-mining algorithm. We uncovered the protein-protein associations that are implicated in important cellular processes including genome integrity, DNA repair, transcriptional regulation, invasion, and pathogenesis, thus demonstrating the utility of this method. The URL of the source code for super-sequence mining method is http://www.cs.utsa.edu/~korkmaz/research/heavy-path-mining/.

Keywords: Bioinformatics; Drug target; Genomics; Heavy path mining; Malaria; Systems biology.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Computational Biology
  • DNA Repair / genetics
  • Gene Expression Regulation
  • Genome*
  • Malaria / genetics*
  • Malaria / parasitology
  • Plasmodium falciparum / genetics*
  • Plasmodium falciparum / pathogenicity
  • Systems Biology