<scp>AutoRevDock</scp> : An open‐source toolkit for scalable reverse docking

Reverse docking is a pivotal computational strategy for drug repurposing and polypharmacology studies, yet existing tools often suffer from limitations in throughput, accuracy, and reliance on centralized servers. To overcome these challenges, we present AutoRevDock, an open-source Python toolkit designed to streamline and enhance the reverse docking workflow. Key features include: (1) support for two established docking engines (AutoDock Vina and idock) with a hybrid scoring scheme (Vina_SFCT, combining the Vina score with a scoring function correction term (SFCT)); (2) pre-processed target libraries covering the human proteome and DrugBank pharmacologically active targets; (3) support for custom target libraries and fully automated local execution. Benchmark evaluations demonstrate that idock operates over 40 times faster than AutoDock Vina. For multiple-target drugs, Vina_SFCT outperforms the default scoring function in identifying biologically relevant targets. Furthermore, incorporating protein family information leads to increased hit rates, suggesting enhanced predictive power for real-world applications. By combining robust methodology with user-centric design, AutoRevDock offers a scalable solution for high-throughput target fishing in drug discovery. The toolkit is freely available at https://github.com/AI4Bio-GuoLAB/AutoRevDock.git.

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Publication Details

Journal
Protein Science
Published
2025-10-22
DOI
https://doi.org/10.1002/pro.70358
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

AutoRevDock : An open‐source toolkit for scalable reverse docking

Jingjing Guo, Liangzhen Zheng, Yuguang Mu, Qing Luo
Protein Science
Computational Drug Discovery Methods
article

AutoRevDock : An open‐source toolkit for scalable reverse docking

Jingjing Guo, Liangzhen Zheng, Yuguang Mu, Qing Luo
article en

Abstract

Reverse docking is a pivotal computational strategy for drug repurposing and polypharmacology studies, yet existing tools often suffer from limitations in throughput, accuracy, and reliance on centralized servers. To overcome these challenges, we present AutoRevDock, an open-source Python toolkit designed to streamline and enhance the reverse docking workflow. Key features include: (1) support for two established docking engines (AutoDock Vina and idock) with a hybrid scoring scheme (Vina_SFCT, combining the Vina score with a scoring function correction term (SFCT)); (2) pre-processed target libraries covering the human proteome and DrugBank pharmacologically active targets; (3) support for custom target libraries and fully automated local execution. Benchmark evaluations demonstrate that idock operates over 40 times faster than AutoDock Vina. For multiple-target drugs, Vina_SFCT outperforms the default scoring function in identifying biologically relevant targets. Furthermore, incorporating protein family information leads to increased hit rates, suggesting enhanced predictive power for real-world applications. By combining robust methodology with user-centric design, AutoRevDock offers a scalable solution for high-throughput target fishing in drug discovery. The toolkit is freely available at https://github.com/AI4Bio-GuoLAB/AutoRevDock.git.

Protein ScienceVol. 34(11)
Nanyang Technological University (SG), Lifetech Scientific (China) (CN), Macao Polytechnic University (MO)
Openalex Percentile: Top 68%
Computational Drug Discovery Methods
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