AlphaFold predicts the most complex protein knot and composite protein knots.

Journal: Protein science : a publication of the Protein Society
Published Date:

Abstract

The computer artificial intelligence system AlphaFold has recently predicted previously unknown three-dimensional structures of thousands of proteins. Focusing on the subset with high-confidence scores, we algorithmically analyze these predictions for cases where the protein backbone exhibits rare topological complexity, that is, knotting. Amongst others, we discovered a 7 -knot, the most topologically complex knot ever found in a protein, as well several six-crossing composite knots comprised of two methyltransferase or carbonic anhydrase domains, each containing a simple trefoil knot. These deeply embedded composite knots occur evidently by gene duplication and interconnection of knotted dimers. Finally, we report two new five-crossing knots including the first 5 -knot. Our list of analyzed structures forms the basis for future experimental studies to confirm these novel-knotted topologies and to explore their complex folding mechanisms.

Authors

  • Maarten A Brems
    Department of Physics, Johannes Gutenberg University Mainz, Mainz, Germany.
  • Robert Runkel
    Department of Physics, Johannes Gutenberg University Mainz, Mainz, Germany.
  • Todd O Yeates
    UCLA-DOE Institute for Genomics and Proteomics, University of California Los Angeles, Los Angeles, California, USA.
  • Peter Virnau
    Department of Physics, Johannes Gutenberg University Mainz, Mainz, Germany.