Given a set of alternative models for a specific protein sequence, the model quality assessment (MQA) problem asks for an assignment of scores to each model in the set. A good MQA program assigns these scores such that they correlate well with real quality of the models, ideally scoring best that model which is closest to the true structure. In this article, we present a new approach for addressing the MQA problem. It is based on distance constraints extracted from alignments to templates of known structure, and is implemented in the Undertaker program for protein structure prediction. One novel feature is that we extract noncontact constraints as well as contact constraints. We describe how the distance constraint extraction is done and we show how they can be used to address the MQA problem. We have compared our method on CASP7 targets and the results show that our method is at least comparable with the best MQA methods that were assessed at CASP7. We also propose a new evaluation measure, Kendall's tau, that is more interpretable than conventional measures used for evaluating MQA methods (Pearson's r and Spearman's rho). We show clear examples where Kendall's tau agrees much more with our intuition of a correct MQA, and we therefore propose that Kendall's tau be used for future CASP MQA assessments.
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http://dx.doi.org/10.1002/prot.22262 | DOI Listing |
Methods Mol Biol
March 2023
School of Biological Sciences, University of Reading, Reading, UK.
Protein structure modeling is one of the most advanced and complex processes in computational biology. One of the major problems for the protein structure prediction field has been how to estimate the accuracy of the predicted 3D models, on both a local and global level, in the absence of known structures. We must be able to accurately measure the confidence that we have in the quality predicted 3D models of proteins for them to become widely adopted by the general bioscience community.
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May 2009
Department of Computer Science, University of Copenhagen, Copenhagen, Denmark.
Given a set of alternative models for a specific protein sequence, the model quality assessment (MQA) problem asks for an assignment of scores to each model in the set. A good MQA program assigns these scores such that they correlate well with real quality of the models, ideally scoring best that model which is closest to the true structure. In this article, we present a new approach for addressing the MQA problem.
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