PC2P
PC2P predicts protein complexes in protein-protein interaction networks (PPINs) by partitioning networks into biclique spanned subgraphs to capture both sparse and dense complex structures.
Key Features:
- Network clustering for PPINs: Operates on protein-protein interaction networks to detect candidate protein complexes.
- Biclique spanned subgraph modeling: Formalizes protein complexes as biclique spanned subgraphs rather than solely dense subgraphs.
- Coherent partition via minimum-edge removal: Partitions the network by removing the minimum number of edges required to achieve a coherent partition into biclique spanned subgraphs.
- Parameter-free greedy approximation algorithm: Uses a parameter-free greedy approximation algorithm to address the computational intractability of finding an optimal coherent partition.
- Handles sparse and dense structures: Explicitly accounts for both sparse and dense subgraph structures present in known complexes.
- Modular structure identification: Identifies modular structures within networks as a prerequisite for complex prediction.
- Benchmark performance on yeast and human gold standards: Demonstrated improved performance relative to other methods on analyzed PPI networks and gold standards, with reported gains on 75% of yeast and 100% of human cases.
- Functional coherence assessment: Maintains high Gene Ontology (GO) semantic similarity and enrichment scores for predicted complexes.
Scientific Applications:
- Protein complex prediction: Predicts candidate protein complexes from PPINs for downstream biological analysis.
- PPI network structure analysis: Analyzes modular and biclique-based substructures in yeast and human PPI networks and gold standards.
- Functional validation of predicted complexes: Supports evaluation of predicted complexes using GO semantic similarity and enrichment metrics.
Methodology:
Partition the network into biclique spanned subgraphs by removing the minimum number of edges to obtain a coherent partition, and approximate the intractable optimal partition using a parameter-free greedy algorithm that leverages properties of biclique spanned subgraphs.
Topics
Details
- Tool Type:
- library
- Programming Languages:
- Python
- Added:
- 3/19/2021
- Last Updated:
- 11/24/2024
Operations
Publications
Omranian S, Angeleska A, Nikoloski Z. PC2P: parameter-free network-based prediction of protein complexes. Bioinformatics. 2021;37(1):73-81. doi:10.1093/bioinformatics/btaa1089. PMID:33416831. PMCID:PMC8034538.
PMID: 33416831
PMCID: PMC8034538
Funding: - European Union’s Horizon 2020 research and innovation programme: 739582
- FPA: 664620
- European Union’s Horizon 2020 research and innovation program: 739582