SiteMatcher: A Web Server for Structure-Based Drug Design Using Protein–Ligand Interaction Patterns

With the rapid growth of structural data in the Protein Data Bank, efficient mining and utilization of protein-ligand interaction pattern information from these structures can advance rational drug design. Here, we present SiteMatcher, a web server that integrates a curated repository of protein-ligand interaction motifs from the Protein Data Bank with an automated fragment-grafting engine to facilitate structure-based ligand design. The engine identifies motifs similar to user-defined local protein sites, extracts ligand fragments from these motifs, and merges them─either directly or via suitable linkers─with the seed compound to produce ligands complementary to the target pocket. By leveraging site similarity-based fragment reuse, SiteMatcher helps users explore diverse ligand design strategies efficiently. We hope that SiteMatcher will serve as a practical tool for medicinal chemists. The server is freely available at https://sitematcher.xundrug.cn.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2025-11-28
DOI
https://doi.org/10.1021/acs.jcim.5c02173
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

SiteMatcher: A Web Server for Structure-Based Drug Design Using Protein–Ligand Interaction Patterns

Zhihan Zhang, Xiaolin Pan, Yi Wu, Dongliang Ke et al.
Journal of Chemical Information and Modeling
Computational Drug Discovery Methods
article

SiteMatcher: A Web Server for Structure-Based Drug Design Using Protein–Ligand Interaction Patterns

Zhihan Zhang, Xiaolin Pan, Yi Wu, Dongliang Ke, Changge Ji, Xingyu Wang, Cheqing Jin, Xudong Xiao, Weiyu Zhou
article en

Abstract

With the rapid growth of structural data in the Protein Data Bank, efficient mining and utilization of protein-ligand interaction pattern information from these structures can advance rational drug design. Here, we present SiteMatcher, a web server that integrates a curated repository of protein-ligand interaction motifs from the Protein Data Bank with an automated fragment-grafting engine to facilitate structure-based ligand design. The engine identifies motifs similar to user-defined local protein sites, extracts ligand fragments from these motifs, and merges them─either directly or via suitable linkers─with the seed compound to produce ligands complementary to the target pocket. By leveraging site similarity-based fragment reuse, SiteMatcher helps users explore diverse ligand design strategies efficiently. We hope that SiteMatcher will serve as a practical tool for medicinal chemists. The server is freely available at https://sitematcher.xundrug.cn.

Journal of Chemical Information and ModelingVol. 65(24)
New York University Shanghai (CN), East China Normal University (CN)
Openalex Percentile: Top 63%
Computational Drug Discovery Methods
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