paper-with-me

Papers

GPU-Accelerated Drug Discovery with Docking on the Summit Supercomputer: Porting, Optimization, and Application to COVID-19 Research

2020-07-06 · Scott LeGrand, Aaron Scheinberg, Andreas F. Tillack, Mathialakan Thavappiragasam, Josh V. Vermaas, Rupesh Agarwal, Jeff Larkin, Duncan Poole, Diogo Santos-Martins, Leonardo Solis-Vasquez, Andreas Koch, Stefano Forli, Oscar Hernandez, Jeremy C. Smith, Ada Sedova

Protein-ligand docking is an in silico tool used to screen potential drug compounds for their ability to bind to a given protein receptor within a drug-discovery campaign. Experimental drug screening is expensive and time consuming, and it is desirable to carry out large scale docking calculations in a high-throughput manner to narrow the experimental search space. Few of the existing computational docking tools were designed with high performance computing in mind. Therefore, optimizations to maximize use of high-performance computational resources available at leadership-class computing facilities enables these facilities to be leveraged for drug discovery. Here we present the porting, optimization, and validation of the AutoDock-GPU program for the Summit supercomputer, and its application to initial compound screening efforts to target proteins of the SARS-CoV-2 virus responsible for the current COVID-19 pandemic.

📄 PDF Abstract BibTeX arXiv:2007.03678

Code (0)

등록된 구현이 없습니다.

Tasks

Drug DiscoveryGPU

Similar Papers 제목 키워드 기반

Transferable Graph Neural Fingerprint Models for Quick Response to Future Bio-Threats

2023-07-17 · Wei Chen, Yihui Ren, Ai Kagawa, Matthew R. Carbone 외

Fast screening of drug molecules based on the ligand binding affinity is an important step in the drug discovery pipeline. Graph neural fingerprint is a promising method for developing molecular docking surrogates with h…

Drug DiscoveryMolecular Docking

Scalable High-Fidelity Macromolecular Docking for GPU-Accelerated Supercomputers

2026-08-07 · Xiangyu Meng, Peng Chen, Mingzhen Li, Jianmin Wang 외 arxiv

Flexible macromolecular docking offers high-fidelity predictions of biomolecular interactions, but remains prohibitively expensive at scale. Among existing approaches, LightDock leverages Glowworm Swarm Optimization (GSO…

Docking-based Virtual Screening with Multi-Task Learning

2021-11-18 · Zijing Liu, Xianbin Ye, Xiaomin Fang, Fan Wang 외

Machine learning shows great potential in virtual screening for drug discovery. Current efforts on accelerating docking-based virtual screening do not consider using existing data of other previously developed targets. T…

BIG-bench Machine LearningDrug DiscoveryMulti-Task Learning

Using Bayesian Optimization to Accelerate Virtual Screening for the Discovery of Therapeutics Appropriate for Repurposing for COVID-19

2020-05-11 · Edward O. Pyzer-Knapp

The novel Wuhan coronavirus known as SARS-CoV-2 has brought almost unprecedented effects for a non-wartime setting, hitting social, economic and health systems hard.~ Being able to bring to bear pharmaceutical interventi…

Bayesian Optimization

DSDP: A Blind Docking Strategy Accelerated by GPUs

2023-03-16 · Yupeng Huang, Hong Zhang, Siyuan Jiang, Dajiong Yue 외

Virtual screening, including molecular docking, plays an essential role in drug discovery. Many traditional and machine-learning based methods are available to fulfil the docking task. The traditional docking methods are…

Blind DockingDrug DiscoveryMolecular Docking