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Seeing the Trees through the Forest

Journal Contribution - Journal Article

Subtitle:Sequence-based Homo- and Heteromeric Protein-protein Interaction sites prediction using Random Forest

Motivation: Genome sequencing is producing an ever-increasing amount of associated protein sequences. Few of these sequences have experimentally validated annotations, however, and computational predictions are becoming increasingly successful in producing such annotations. One key challenge remains the prediction of the amino acids in a given protein sequence that are involved in protein-protein interactions. Such predictions are typically based on machine learning methods that take advantage of the properties and sequence positions of amino acids that are known to be involved in interaction. In this paper, we evaluate the importance of various features using Random Forest (RF), and include as a novel feature backbone flexibility predicted from sequences to further optimise protein interface prediction.

Results: We observe that there is no single sequence feature that enables pinpointing interacting sites in our Random Forest models. However, combining different properties does increase the performance of interface prediction. Our homomeric-trained RF interface predictor is able to distinguish interface from non-interface residues with an area under the ROC curve of 0.72 in a homomeric test-set. The heteromeric-trained RF interface predictor performs better than existing predictors on a independent heteromeric test-set. We trained a more general predictor on the combined homomeric and heteromeric dataset, and show that in addition to predicting homomeric interfaces, it is also able to pinpoint interface residues in heterodimers. This suggests that our random forest model and the features included capture common properties of both homodimer and heterodimer interfaces.

Availability and Implementation: The predictors and test datasets used in our analyses are freely available ( http://www.ibi.vu.nl/downloads/RF_PPI/ ).

Contact: k.a.feenstra@vu.nl.

Supplementary information: Supplementary data are available at Bioinformatics online.

Journal: Bioinformatics
ISSN: 1367-4803
Issue: 10
Volume: 33
Pages: 1479-1487
Publication year:2017
Keywords:Algorithms, Computational Biology/methods, Models, Statistical, Protein Interaction Domains and Motifs, Protein Interaction Mapping/methods, Protein Multimerization, ROC Curve, Sequence Analysis, Protein/methods
CSS-citation score:1