Improved protein structure prediction using predicted interresidue orientations

Jianyi Yang, Ivan Anishchenko, Hahnbeom Park, Zhenling Peng, Sergey Ovchinnikov, David Baker

Proceedings of the National Academy of Sciences · 2020 · 1.6K citations · 26 references

DOIFull text

Open access

Concepts

TL;DR

The prediction of interresidue contacts and distances from coevolutionary data using deep learning has considerably advanced protein structure prediction. The study develops a deep residual network to predict interresidue orientations and a Rosetta‑constrained protocol to generate accurate structure models guided by these restraints. Using a deep residual network and Rosetta‑constrained energy minimization, the method predicts interresidue orientations and distances to generate structure models. Benchmark tests on CASP13 and CAMEO sets show the method outperforms all previous methods, accurately identifies key fold‑determining residues in de novo‑designed proteins, and provides a quantitative measure of protein structure ideality, making it broadly useful for prediction and design.

Abstract

The prediction of interresidue contacts and distances from coevolutionary data using deep learning has considerably advanced protein structure prediction. Here, we build on these advances by developing a deep residual network for predicting interresidue orientations, in addition to distances, and a Rosetta-constrained energy-minimization protocol for rapidly and accurately generating structure models guided by these restraints. In benchmark tests on 13th Community-Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction (CASP13)- and Continuous Automated Model Evaluation (CAMEO)-derived sets, the method outperforms all previously described structure-prediction methods. Although trained entirely on native proteins, the network consistently assigns higher probability to de novo-designed proteins, identifying the key fold-determining residues and providing an independent quantitative measure of the “ideality” of a protein structure. The method promises to be useful for a broad range of protein structure prediction and design problems.

References

26