Protein-ligand binding affinity prediction exploiting sequence constituent homology.

Journal: Bioinformatics (Oxford, England)
Published Date:

Abstract

MOTIVATION: Molecular docking is a commonly used approach for estimating binding conformations and their resultant binding affinities. Machine learning has been successfully deployed to enhance such affinity estimations. Many methods of varying complexity have been developed making use of some or all the spatial and categorical information available in these structures. The evaluation of such methods has mainly been carried out using datasets from PDBbind. Particularly the Comparative Assessment of Scoring Functions (CASF) 2007, 2013, and 2016 datasets with dedicated test sets. This work demonstrates that only a small number of simple descriptors is necessary to efficiently estimate binding affinity for these complexes without the need to know the exact binding conformation of a ligand.

Authors

  • Abbi Abdel-Rehim
    Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Oghenejokpeme Orhobor
    The National Institute of Agricultural Botany, Cambridge CB3 0LE, United Kingdom.
  • Lou Hang
    Department of Mathematics, University College London, London WC1H 0AY, United Kingdom.
  • Hao Ni
    Hangzhou YITU Healthcare Technology Co. Ltd, Hangzhou, China.
  • Ross D King
    3Department of Biology and Biological Engineering, Division of Systems and Synthetic Biology, Chalmers University of Technology, Kemivägen 10, SE-412 96 Gothenburg, Sweden.