Improving fragment-based ab initio protein structure assembly using low-accuracy contact-map predictions
S. M. Mortuza,
Wei Zheng,
Chengxin Zhang,
Yang Li,
Robin Pearce and
Yang Zhang ()
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S. M. Mortuza: University of Michigan
Wei Zheng: University of Michigan
Chengxin Zhang: University of Michigan
Yang Li: University of Michigan
Robin Pearce: University of Michigan
Yang Zhang: University of Michigan
Nature Communications, 2021, vol. 12, issue 1, 1-12
Abstract:
Abstract Sequence-based contact prediction has shown considerable promise in assisting non-homologous structure modeling, but it often requires many homologous sequences and a sufficient number of correct contacts to achieve correct folds. Here, we developed a method, C-QUARK, that integrates multiple deep-learning and coevolution-based contact-maps to guide the replica-exchange Monte Carlo fragment assembly simulations. The method was tested on 247 non-redundant proteins, where C-QUARK could fold 75% of the cases with TM-scores (template-modeling scores) ≥0.5, which was 2.6 times more than that achieved by QUARK. For the 59 cases that had either low contact accuracy or few homologous sequences, C-QUARK correctly folded 6 times more proteins than other contact-based folding methods. C-QUARK was also tested on 64 free-modeling targets from the 13th CASP (critical assessment of protein structure prediction) experiment and had an average GDT_TS (global distance test) score that was 5% higher than the best CASP predictors. These data demonstrate, in a robust manner, the progress in modeling non-homologous protein structures using low-accuracy and sparse contact-map predictions.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25316-w
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DOI: 10.1038/s41467-021-25316-w
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