Evidence map›Paper›PMID 24731387›Full record

ArticleBMC structural biology2014

Designing and evaluating the MULTICOM protein local and global model quality prediction methods in the CASP10 experiment.

Renzhi Cao, Zheng Wang, Jianlin Cheng

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Article in BMC structural biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

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27citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

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  16. Identifying NMolecular genetics and genomics : MGG · 2016
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Renzhi Cao
Zheng Wang
Jianlin ChengComputer Science Department, University of Missouri, Columbia, Missouri 65211, USA. chengji@missouri.edu.

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 R01GM093123
6 · The paper itself

Abstract

backgroundProtein model quality assessment is an essential component of generating and using protein structural models. During the Tenth Critical Assessment of Techniques for Protein Structure Prediction (CASP10), we developed and tested four automated methods (MULTICOM-REFINE, MULTICOM-CLUSTER, MULTICOM-NOVEL, and MULTICOM-CONSTRUCT) that predicted both local and global quality of protein structural models.

resultsMULTICOM-REFINE was a clustering approach that used the average pairwise structural similarity between models to measure the global quality and the average Euclidean distance between a model and several top ranked models to measure the local quality. MULTICOM-CLUSTER and MULTICOM-NOVEL were two new support vector machine-based methods of predicting both the local and global quality of a single protein model. MULTICOM-CONSTRUCT was a new weighted pairwise model comparison (clustering) method that used the weighted average similarity between models in a pool to measure the global model quality. Our experiments showed that the pairwise model assessment methods worked better when a large portion of models in the pool were of good quality, whereas single-model quality assessment methods performed better on some hard targets when only a small portion of models in the pool were of reasonable quality.

conclusionsSince digging out a few good models from a large pool of low-quality models is a major challenge in protein structure prediction, single model quality assessment methods appear to be poised to make important contributions to protein structure modeling. The other interesting finding was that single-model quality assessment scores could be used to weight the models by the consensus pairwise model comparison method to improve its accuracy.

Indexed as

Protein ConformationSupport Vector MachineComputational BiologyDatabases, ProteinModels, MolecularProteinsSoftwareProteins

Identifiers

PMID24731387
PMCPMC3996498

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LicenceCC BY
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Registered trials

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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.