4.8 Article

Accurate prediction of protein structures and interactions using a three-track neural network

Journal

SCIENCE
Volume 373, Issue 6557, Pages 871-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abj8754

Keywords

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Funding

  1. Microsoft
  2. Open Philanthropy
  3. Schmidt Futures program
  4. Washington Research Foundation
  5. National Science Foundation [DBI 1937533]
  6. Wellcome Trust [209407/Z/17/Z]
  7. National Institutes of Health [P01GM063210, DP5OD026389, RO1-AI51321, GM127390]
  8. Mathers Foundation
  9. Canadian Institute of Health Research (CIHR) [168998, 168907]
  10. Welch Foundation [I-1505]
  11. Global Challenges Research Fund (GCRF) through Science & Technology Facilities Council (STFC) [ST/R002754/1]
  12. Austrian Science Fund (FWF) [P29432, DOC50]
  13. STFC [ST/R002754/1] Funding Source: UKRI
  14. Austrian Science Fund (FWF) [P29432, DOC50] Funding Source: Austrian Science Fund (FWF)

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Through the three-track network, we achieved accuracies approaching those of DeepMind in CASP14, enabling rapid solution of challenging x-ray crystallography and cryo-electron microscopy structure modeling problems, and providing insights into the functions of proteins with currently unknown structure.
DeepMind presented notably accurate predictions at the recent 14th Critical Assessment of Structure Prediction (CASP14) conference. We explored network architectures that incorporate related ideas and obtained the best performance with a three-track network in which information at the one-dimensional (1D) sequence level, the 2D distance map level, and the 3D coordinate level is successively transformed and integrated. The three-track network produces structure predictions with accuracies approaching those of DeepMind in CASP14, enables the rapid solution of challenging x-ray crystallography and cryo-electron microscopy structure modeling problems, and provides insights into the functions of proteins of currently unknown structure. The network also enables rapid generation of accurate protein-protein complex models from sequence information alone, short-circuiting traditional approaches that require modeling of individual subunits followed by docking. We make the method available to the scientific community to speed biological research.

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