Evidence map›Paper›PMID 29334889›Full record

ArticleBMC bioinformatics2018

Protein-protein interface hot spots prediction based on a hybrid feature selection strategy.

Yanhua Qiao, Yi Xiong, Hongyun Gao, Xiaolei Zhu, Peng Chen

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Review
  2. PPI-hotspoteLife · 2024
    Article
  3. Article
  4. Interface engineering of cellobiose dehydrogenase improves interdomain electron transfer.Protein science : a publication of the Protein Society · 2023
    Article
  5. Article
  6. Article
  7. Data analysis methods for defining biomarkers from omics data.Analytical and bioanalytical chemistry · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Spectral analysis of molecular dynamics simulations on PDZ: MD sectors.Journal of biomolecular structure & dynamics · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Prediction of Anticancer Peptides Using a Low-Dimensional Feature Model.Frontiers in bioengineering and biotechnology · 2020
    Article
  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.

Yanhua QiaoSchool of Life Sciences, Anhui University, Hefei, Anhui, 230601, China.
Yi XiongState Key Laboratory of Microbial Metabolism, Shanghai JiaoTong University, Shanghai, 200240, China.
Hongyun GaoInformation and Engineering College, Dalian University, Dalian, Liaoning, 116622, China.
Xiaolei ZhuSchool of Life Sciences, Anhui University, Hefei, Anhui, 230601, China. xlzhu_mdl@hotmail.com.ORCID 0000-0002-1967-2806
Peng ChenInstitute of Health Sciences, Anhui University, Hefei, Anhui, 230601, China. pchen@ahu.edu.cn.

Funding

Doctoral Fund of Liaoning Province 201601296National Natural Science Foundation of China 11626052National Natural Science Foundation of China 31601074National Natural Science Foundation of China 61300058National Natural Science Foundation of China 61672035National Natural Science Foundation of China (CN) 21403002
6 · The paper itself

Abstract

backgroundHot spots are interface residues that contribute most binding affinity to protein-protein interaction. A compact and relevant feature subset is important for building machine learning methods to predict hot spots on protein-protein interfaces. Although different methods have been used to detect the relevant feature subset from a variety of features related to interface residues, it is still a challenge to detect the optimal feature subset for building the final model.

resultsIn this study, three different feature selection methods were compared to propose a new hybrid feature selection strategy. This new strategy was proved to effectively reduce the feature space when we were building the prediction models for identifying hotspot residues. It was tested on eighty-two features, both conventional and newly proposed. According to the strategy, combining the feature subsets selected by decision tree and mRMR (maximum Relevance Minimum Redundancy) individually, we were able to build a model with 6 features by using a PSFS (Pseudo Sequential Forward Selection) process. Compared with other state-of-art methods for the independent test set, our model had shown better or comparable predictive performances (with F-measure 0.622 and recall 0.821). Analysis of the 6 features confirmed that our newly proposed feature CNSV_REL1 was important for our model. The analysis also showed that the complementarity between features should be considered as an important aspect when conducting the feature selection.

conclusionIn this study, most important of all, a new strategy for feature selection was proposed and proved to be effective in selecting the optimal feature subset for building prediction models, which can be used to predict hot spot residues on protein-protein interfaces. Moreover, two aspects, the generalization of the single feature and the complementarity between features, were proved to be of great importance and should be considered in feature selection methods. Finally, our newly proposed feature CNSV_REL1 had been proved an alternative and effective feature in predicting hot spots by our study. Our model is available for users through a webserver: http://zhulab.ahu.edu.cn/iPPHOT/ .

Indexed as

AlgorithmsComputational BiologyDatabases, ProteinHumansProteinsSupport Vector MachineProteinsFeature selectionHot spotProtein-protein InterfaceResidue conservation

Identifiers

PMID29334889
PMCPMC5769548

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.