Evidence map›Paper›PMID 19419562›Full record

ArticleBMC structural biology2009

Improving consensus contact prediction via server correlation reduction.

Xin Gao, Dongbo Bu, Jinbo Xu, Ming Li

Abstract read
In one paragraph

Article in BMC structural biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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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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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xin GaoDavid R, Cheriton School of Computer Science, University of Waterloo, N2L3G1, Canada. x4gao@cs.uwaterloo.ca
Dongbo Bu
Jinbo Xu
Ming Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein inter-residue contacts play a crucial role in the determination and prediction of protein structures. Previous studies on contact prediction indicate that although template-based consensus methods outperform sequence-based methods on targets with typical templates, such consensus methods perform poorly on new fold targets. However, we find out that even for new fold targets, the models generated by threading programs can contain many true contacts. The challenge is how to identify them.

resultsIn this paper, we develop an integer linear programming model for consensus contact prediction. In contrast to the simple majority voting method assuming that all the individual servers are equally important and independent, the newly developed method evaluates their correlation by using maximum likelihood estimation and extracts independent latent servers from them by using principal component analysis. An integer linear programming method is then applied to assign a weight to each latent server to maximize the difference between true contacts and false ones. The proposed method is tested on the CASP7 data set. If the top L/5 predicted contacts are evaluated where L is the protein size, the average accuracy is 73%, which is much higher than that of any previously reported study. Moreover, if only the 15 new fold CASP7 targets are considered, our method achieves an average accuracy of 37%, which is much better than that of the majority voting method, SVM-LOMETS, SVM-SEQ, and SAM-T06. These methods demonstrate an average accuracy of 13.0%, 10.8%, 25.8% and 21.2%, respectively.

conclusionReducing server correlation and optimally combining independent latent servers show a significant improvement over the traditional consensus methods. This approach can hopefully provide a powerful tool for protein structure refinement and prediction use.

Indexed as

Amino Acid SequenceConsensus SequenceSoftwareArtificial IntelligenceBinding SitesComputational BiologyComputer SimulationModels, MolecularProgramming, LinearProtein BindingProteinsSequence Analysis, ProteinProteins

Identifiers

PMID19419562
PMCPMC2689239

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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.