Affinity prediction using deep learning based on SMILES input for D3R grand challenge 4.

Journal: Journal of computer-aided molecular design
Published Date:

Abstract

Modern molecular docking comprises the prediction of pose and affinity. Prediction of docking poses is required for affinity prediction when three-dimensional coordinates of the ligand have not been provided. However, a large number of feature engineering is required for existing methods. In addition, there is a need for a robust model for the sequential combination of pose and affinity prediction due to the probabilistic deviation of the ligand position issue. We propose a pipeline using a bipartite graph neural network and transfer learning trained on a re-docking dataset. We evaluated our model on the released data from drug design data resource grand challenge 4 (D3R GC4). The two target protein data provided by the challenge have different patterns. The model outperformed the best participant by 9% on the BACE target protein from stage 2. Further, our model showed competitive performance on the CatS target protein.

Authors

  • Sangrak Lim
    Department of Computer Science and Engineering, Korea University, Anam-dong 5-ga, Seongbuk-gu, Seoul, South Korea.
  • Yong Oh Lee
    Smart Convergence Group, KIST Europe, Saarbrücken, 66123, Germany.
  • Juyong Yoon
    Kist Europe, Campus E7 1 66123, Saarbrücken , Germany.
  • Young Jun Kim
    3Department of Food and Biotechnology, Korea University, Sejong City, 30019 Republic of Korea.