Evidence map›Paper›PMID 31521132›Full record

ArticleBMC bioinformatics2019

Identifying protein complexes based on an edge weight algorithm and core-attachment structure.

Rongquan Wang, Guixia Liu, Caixia Wang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Therapeutic RNA Delivery for COVID and Other Diseases.Advanced healthcare materials · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Rongquan WangCollege of Computer Science and Technology, Jilin University, No. 2699 Qianjin Street, Changchun, 130012, China.
Guixia LiuCollege of Computer Science and Technology, Jilin University, No. 2699 Qianjin Street, Changchun, 130012, China. liugx@jlu.edu.cn.ORCID http://orcid.org/0000-0002-3375-9561
Caixia WangSchool of International Economics, China Foreign Affairs University, 24 Zhanlanguan Road, Xicheng District, Beijing, 100037, China.

Funding

National Natural Science Foundation of China 61373051National Natural Science Foundation of China 61502343National Natural Science Foundation of China 61772226Rongquan Wang 10183201835
6 · The paper itself

Abstract

backgroundProtein complex identification from protein-protein interaction (PPI) networks is crucial for understanding cellular organization principles and functional mechanisms. In recent decades, numerous computational methods have been proposed to identify protein complexes. However, most of the current state-of-the-art studies still have some challenges to resolve, including their high false-positives rates, incapability of identifying overlapping complexes, lack of consideration for the inherent organization within protein complexes, and absence of some biological attachment proteins.

resultsIn this paper, to overcome these limitations, we present a protein complex identification method based on an edge weight method and core-attachment structure (EWCA) which consists of a complex core and some sparse attachment proteins. First, we propose a new weighting method to assess the reliability of interactions. Second, we identify protein complex cores by using the structural similarity between a seed and its direct neighbors. Third, we introduce a new method to detect attachment proteins that is able to distinguish and identify peripheral proteins and overlapping proteins. Finally, we bind attachment proteins to their corresponding complex cores to form protein complexes and discard redundant protein complexes. The experimental results indicate that EWCA outperforms existing state-of-the-art methods in terms of both accuracy and p-value. Furthermore, EWCA could identify many more protein complexes with statistical significance. Additionally, EWCA could have better balance accuracy and efficiency than some state-of-the-art methods with high accuracy.

conclusionsIn summary, EWCA has better performance for protein complex identification by a comprehensive comparison with twelve algorithms in terms of different evaluation metrics. The datasets and software are freely available for academic research at https://github.com/RongquanWang/EWCA .

Indexed as

Protein Interaction MapsSoftwareAlgorithmsComputational BiologyHumansProtein ConformationSaccharomyces cerevisiaeCore-attachment structureProtein complexesProtein-protein interaction networksSpurious interactionsStructural similarity

Identifiers

PMID31521132
PMCPMC6744658

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.