ArticlePloS one2013
Benchmarking human protein complexes to investigate drug-related systems and evaluate predicted protein complexes.
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 8 papers.
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8 citing papers in PubMed, 17 citations in OpenAlex.
- Resolving missing protein problems using functional class scoring.Scientific reports · 2022Article
- Detection of Protein Complexes Based on Penalized Matrix Decomposition in a Sparse Protein⁻Protein Interaction Network.Molecules (Basel, Switzerland) · 2018Article
- A common neighbor based technique to detect protein complexes in PPI networks.Journal, genetic engineering & biotechnology · 2018Article
- Protein complex finding and ranking: An application to Alzheimer's disease.Journal of biosciences · 2017Article
- Systems-level analysis of human aging genes shed new light on mechanisms of aging.Human molecular genetics · 2016Article
- Detecting overlapping protein complexes by rough-fuzzy clustering in protein-protein interaction networks.PloS one · 2014Article
- Integration strategy is a key step in network-based analysis and dramatically affects network topological properties and inferring outcomes.BioMed research international · 2014Article
- Contemporary network proteomics and its requirements.Biology · 2013Article
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Authors and funding
6 authors at 4 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Protein complexes are key entities to perform cellular functions. Human diseases are also revealed to associate with some specific human protein complexes. In fact, human protein complexes are widely used for protein function annotation, inference of human protein interactome, disease gene prediction, and so on. Therefore, it is highly desired to build an up-to-date catalogue of human complexes to support the research in these applications. Protein complexes from different databases are as expected to be highly redundant. In this paper, we designed a set of concise operations to compile these redundant human complexes and built a comprehensive catalogue called CHPC2012 (Catalogue of Human Protein Complexes). CHPC2012 achieves a higher coverage for proteins and protein complexes than those individual databases. It is also verified to be a set of complexes with high quality as its co-complex protein associations have a high overlap with protein-protein interactions (PPI) in various existing PPI databases. We demonstrated two distinct applications of CHPC2012, that is, investigating the relationship between protein complexes and drug-related systems and evaluating the quality of predicted protein complexes. In particular, CHPC2012 provides more insights into drug development. For instance, proteins involved in multiple complexes (the overlapping proteins) are potential drug targets; the drug-complex network is utilized to investigate multi-target drugs and drug-drug interactions; and the disease-specific complex-drug networks will provide new clues for drug repositioning. With this up-to-date reference set of human protein complexes, we believe that the CHPC2012 catalogue is able to enhance the studies for protein interactions, protein functions, human diseases, drugs, and related fields of research. CHPC2012 complexes can be downloaded from http://www1.i2r.a-star.edu.sg/xlli/CHPC2012/CHPC2012.htm.
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