ProfPPldb: Pairs of physical protein-protein interactions predicted for entire proteomes

被引:8
|
作者
Linh Tran [1 ,2 ]
Hamp, Tobias [2 ]
Rost, Burkhard [2 ,3 ]
机构
[1] ICI PLC, Dept Comp, London, England
[2] TUM, Dept Informat Bioinformat & Computat Biol I12, Boltzmannstr, Munich, Germany
[3] TUM, Inst Adv Study TUM IAS, Lichtenbergstr, Munich, Germany
来源
PLOS ONE | 2018年 / 13卷 / 07期
关键词
SEQUENCE-BASED KERNELS; EVOLUTIONARY INFORMATION; DATABASE; NETWORKS; RESOURCE; PROFILES; TOOL;
D O I
10.1371/journal.pone.0199988
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Motivation Protein-protein interactions (PPIs) play a key role in many cellular processes. Most annotations of PPIs mix experimental and computational data. The mix optimizes coverage, but obfuscates the annotation origin. Some resources excel at focusing on reliable experimental data. Here, we focused on new pairs of interacting proteins for several model organisms based solely on sequence-based prediction methods. Results We extracted reliable experimental data about which proteins interact (binary) for eight diverse model organisms from public databases, namely from Escherichia coli, Schizosaccharomyces pombe, Plasmodium falciparum, Drosophila melanogaster, Caenorhabditis elegans, Mus musculus, Rattus norvegicus, Arabidopsis thaliana, and for the previously used Homo sapiens and Saccharomyces cerevisiae. Those data were the base to develop a PPI prediction method for each model organism. The method used evolutionary information through a profile-kernel Support Vector Machine (SVM). With the resulting eight models, we predicted all possible protein pairs in each organism and made the top predictions available through a web application. Almost all of the PPIs made available were predicted between proteins that have not been observed in any interaction, in particular for less wellstudied organisms. Thus, our work complements existing resources and is particularly helpful for designing experiments because of its uniqueness. Experimental annotations and computational predictions are strongly influenced by the fact that some proteins have many partners and others few. To optimize machine learning, recent methods explicitly ignored such a network-structure and rely either on domain knowledge or sequence-only methods. Our approach is independent of domain-knowledge and leverages evolutionary information. The database interface representing our results is accessible from https://rostlab.org/services/ppipair/. The data can also be downloaded from https://figshare.com/collections/ProfPPI-DB/4141784.
引用
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页数:13
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