Machine learning optimization of cross docking accuracy. (June 2016)
- Record Type:
- Journal Article
- Title:
- Machine learning optimization of cross docking accuracy. (June 2016)
- Main Title:
- Machine learning optimization of cross docking accuracy
- Authors:
- Bjerrum, Esben J.
- Abstract:
- Graphical abstract: Highlights: Machine learning method for optimizing docking functions. Alternative score weights for cross-docking with Autodock Vina and Smina. Cross-docking benchmark for realistic estimation of ligand pose prediction accuracy. Abstract: Performance of small molecule automated docking programs has conceptually been divided into docking -, scoring -, ranking - and screening power, which focuses on the crystal pose prediction, affinity prediction, ligand ranking and database screening capabilities of the docking program, respectively. Benchmarks show that different docking programs can excel in individual benchmarks which suggests that the scoring function employed by the programs can be optimized for a particular task. Here the scoring function of Smina is re-optimized towards enhancing the docking power using a supervised machine learning approach and a manually curated database of ligands and cross docking receptor pairs. The optimization method does not need associated binding data for the receptor-ligand examples used in the data set and works with small train sets. The re-optimization of the weights for the scoring function results in a similar docking performance with regard to docking power towards a cross docking test set. A ligand decoy based benchmark indicates a better discrimination between poses with high and low RMSD. The reported parameters for Smina are compatible with Autodock Vina and represent ready-to-use alternative parameters forGraphical abstract: Highlights: Machine learning method for optimizing docking functions. Alternative score weights for cross-docking with Autodock Vina and Smina. Cross-docking benchmark for realistic estimation of ligand pose prediction accuracy. Abstract: Performance of small molecule automated docking programs has conceptually been divided into docking -, scoring -, ranking - and screening power, which focuses on the crystal pose prediction, affinity prediction, ligand ranking and database screening capabilities of the docking program, respectively. Benchmarks show that different docking programs can excel in individual benchmarks which suggests that the scoring function employed by the programs can be optimized for a particular task. Here the scoring function of Smina is re-optimized towards enhancing the docking power using a supervised machine learning approach and a manually curated database of ligands and cross docking receptor pairs. The optimization method does not need associated binding data for the receptor-ligand examples used in the data set and works with small train sets. The re-optimization of the weights for the scoring function results in a similar docking performance with regard to docking power towards a cross docking test set. A ligand decoy based benchmark indicates a better discrimination between poses with high and low RMSD. The reported parameters for Smina are compatible with Autodock Vina and represent ready-to-use alternative parameters for researchers who aim at pose prediction rather than affinity prediction. … (more)
- Is Part Of:
- Computational biology and chemistry. Volume 62(2016)
- Journal:
- Computational biology and chemistry
- Issue:
- Volume 62(2016)
- Issue Display:
- Volume 62, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 62
- Issue:
- 2016
- Issue Sort Value:
- 2016-0062-2016-0000
- Page Start:
- 133
- Page End:
- 144
- Publication Date:
- 2016-06
- Subjects:
- Molecular docking -- Docking power -- Scoring function -- Machine learning optimization -- Smina -- Autodock Vina -- Drug discovery -- Cross docking
Chemistry -- Data processing -- Periodicals
Biology -- Data processing -- Periodicals
Biochemistry -- Data processing
Biology -- Data processing
Molecular biology -- Data processing
Periodicals
Electronic journals
542.85 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14769271 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.compbiolchem.2016.04.005 ↗
- Languages:
- English
- ISSNs:
- 1476-9271
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3390.576700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7783.xml