Evidence map›Paper›PMID 22937126›Full record

ArticlePloS one2012

Prediction of protein-protein interaction sites by random forest algorithm with mRMR and IFS.

Bi-Qing Li, Kai-Yan Feng, Lei Chen, Tao Huang, Yu-Dong Cai

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. ProtInteract: A deep learning framework for predicting protein-protein interactions.Computational and structural biotechnology journal · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Deciphering Pleiotropic Signatures of Regulatory SNPs inInternational journal of molecular sciences · 2022
    Article
  14. Ensemble machine learning model identifies patients with HFpEF from matrix-related plasma biomarkers.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  15. Article
  16. Article
  17. Effective Macrosomia Prediction Using Random Forest Algorithm.International journal of environmental research and public health · 2022
    Article
  18. Article
  19. Deep learning frameworks for protein-protein interaction prediction.Computational and structural biotechnology journal · 2022
    Review
  20. 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

5 authors.

Bi-Qing LiKey Laboratory of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, People's Republic of China.
Kai-Yan Feng
Lei Chen
Tao Huang
Yu-Dong Cai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prediction of protein-protein interaction (PPI) sites is one of the most challenging problems in computational biology. Although great progress has been made by employing various machine learning approaches with numerous characteristic features, the problem is still far from being solved. In this study, we developed a novel predictor based on Random Forest (RF) algorithm with the Minimum Redundancy Maximal Relevance (mRMR) method followed by incremental feature selection (IFS). We incorporated features of physicochemical/biochemical properties, sequence conservation, residual disorder, secondary structure and solvent accessibility. We also included five 3D structural features to predict protein-protein interaction sites and achieved an overall accuracy of 0.672997 and MCC of 0.347977. Feature analysis showed that 3D structural features such as Depth Index (DPX) and surface curvature (SC) contributed most to the prediction of protein-protein interaction sites. It was also shown via site-specific feature analysis that the features of individual residues from PPI sites contribute most to the determination of protein-protein interaction sites. It is anticipated that our prediction method will become a useful tool for identifying PPI sites, and that the feature analysis described in this paper will provide useful insights into the mechanisms of interaction.

Indexed as

AlgorithmsComputational BiologyProtein ConformationProteinsProteins

Identifiers

PMID22937126
PMCPMC3429425

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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.