ArticleIEEE/ACM transactions on computational biology and bioinformatics
Two New Heuristic Methods for Protein Model Quality Assessment.
Article in IEEE/ACM transactions on computational biology and bioinformatics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- AlphaFold model quality self-assessment improvement via deep graph learning.Protein science : a publication of the Protein Society · 2025Article
- Probabilistic divergence of a template-based modelling methodology from the ideal protocol.Journal of molecular modeling · 2021Article
- MUfoldQA_G: High-accuracy protein model QA via retraining and transformation.Computational and structural biotechnology journal · 2021Article
- Machine Learning Approaches for Quality Assessment of Protein Structures.Biomolecules · 2020Review
- PSICA: a fast and accurate web service for protein model quality analysis.Nucleic acids research · 2019Article
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4 authors.
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Abstract
Protein tertiary structure prediction is an important open challenge in bioinformatics and requires effective methods to accurately evaluate the quality of protein 3-D models generated computationally. Many quality assessment (QA) methods have been proposed over the past three decades. However, the accuracy or robustness is unsatisfactory for practical applications. In this paper, two new heuristic QA methods are proposed: MUfoldQA_S and MUfoldQA_C. The MUfoldQA_S is a quasi-single-model QA method that assesses the model quality based on the known protein structures with similar sequences. This algorithm can be directly applied to protein fragments without the necessity of building a full structural model. A BLOSUM-based heuristic is also introduced to help differentiate accurate templates from poor ones. In MUfoldQA_C, the ideas from MUfoldQA_S were combined with the consensus approach to create a multi-model QA method that could also utilize information from existing reference models and have demonstrated improved performance. Extensive experimental results of these two methods have shown significant improvement over existing methods. In addition, both methods have been blindly tested in the CASP12 world-wide competition in the protein structure prediction field and ranked as top performers in their respective categories.
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