Evidence map›Paper›PMID 26072473›Full record

ArticleBioinformatics (Oxford, England)2015

Large-scale model quality assessment for improving protein tertiary structure prediction.

Renzhi Cao, Debswapna Bhattacharya, Badri Adhikari, Jilong Li, Jianlin Cheng

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  9. MUfoldQA_G: High-accuracy protein model QA via retraining and transformation.Computational and structural biotechnology journal · 2021
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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.

Renzhi CaoComputer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA.
Debswapna BhattacharyaComputer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA.
Badri AdhikariComputer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA.
Jilong LiComputer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA.
Jianlin ChengComputer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA Computer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA Computer Science Department, University of Missouri, Columbia, Missouri, 65211, USA, Informatics Institute, University of Missouri, Columbia, Missouri, 65211, USA and C. Bond Life Science Center, University of Missouri, Columbia, Missouri, 65211, USA.

Funding

Integrated Prediction of Protein Struture at 1D, 2D and 3D LevelsR01GM093123 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHENG, JIANLIN · 2010 to 2023
$3.8M
NIGMS NIH HHS R01 GM093123NIGMS NIH HHS R01GM093123
6 · The paper itself

Abstract

motivationSampling structural models and ranking them are the two major challenges of protein structure prediction. Traditional protein structure prediction methods generally use one or a few quality assessment (QA) methods to select the best-predicted models, which cannot consistently select relatively better models and rank a large number of models well.

resultsHere, we develop a novel large-scale model QA method in conjunction with model clustering to rank and select protein structural models. It unprecedentedly applied 14 model QA methods to generate consensus model rankings, followed by model refinement based on model combination (i.e. averaging). Our experiment demonstrates that the large-scale model QA approach is more consistent and robust in selecting models of better quality than any individual QA method. Our method was blindly tested during the 11th Critical Assessment of Techniques for Protein Structure Prediction (CASP11) as MULTICOM group. It was officially ranked third out of all 143 human and server predictors according to the total scores of the first models predicted for 78 CASP11 protein domains and second according to the total scores of the best of the five models predicted for these domains. MULTICOM's outstanding performance in the extremely competitive 2014 CASP11 experiment proves that our large-scale QA approach together with model clustering is a promising solution to one of the two major problems in protein structure modeling. AVAILABILITY AND IMPLEMENTATION: The web server is available at: http://sysbio.rnet.missouri.edu/multicom_cluster/human/.

Indexed as

Models, MolecularProtein Structure, TertiaryCluster AnalysisHumansSoftware

Identifiers

PMID26072473
PMCPMC4553833

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.