ArticlePloS one2013
Prediction of heterodimeric protein complexes from weighted protein-protein interaction networks using novel features and kernel functions.
Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Improving prediction of heterodimeric protein complexes using combination with pairwise kernel.BMC bioinformatics · 2018Article
- Multiple kernels learning-based biological entity relationship extraction method.Journal of biomedical semantics · 2017Article
- Prediction of heterotrimeric protein complexes by two-phase learning using neighboring kernels.BMC bioinformatics · 2014Article
- Heterodimeric protein complex identification by naïve Bayes classifiers.BMC bioinformatics · 2013Article
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4 authors.
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Abstract
Since many proteins express their functional activity by interacting with other proteins and forming protein complexes, it is very useful to identify sets of proteins that form complexes. For that purpose, many prediction methods for protein complexes from protein-protein interactions have been developed such as MCL, MCODE, RNSC, PCP, RRW, and NWE. These methods have dealt with only complexes with size of more than three because the methods often are based on some density of subgraphs. However, heterodimeric protein complexes that consist of two distinct proteins occupy a large part according to several comprehensive databases of known complexes. In this paper, we propose several feature space mappings from protein-protein interaction data, in which each interaction is weighted based on reliability. Furthermore, we make use of prior knowledge on protein domains to develop feature space mappings, domain composition kernel and its combination kernel with our proposed features. We perform ten-fold cross-validation computational experiments. These results suggest that our proposed kernel considerably outperforms the naive Bayes-based method, which is the best existing method for predicting heterodimeric protein complexes.
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