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Updated: May 27, 2026

Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis
Published on: June 20, 2025
FTSite: high accuracy detection of ligand binding sites on unbound protein structures
Chi-Ho Ngan1, David R Hall, Brandon Zerbe
1Department of Biomedical Engineering, Boston University, Boston, MA 02115, USA.
Motivation:
Binding site identification is a classical problem that is important for a range of applications, including the structure-based prediction of function, the elucidation of functional relationships among proteins, protein engineering and drug design. We describe an accurate method of binding site identification, namely FTSite. This method is based on experimental evidence that ligand binding sites also bind small organic molecules of various shapes and polarity. The FTSite algorithm does not rely on any evolutionary or statistical information, but achieves near experimental accuracy: it is capable of identifying the binding sites in over 94% of apo proteins from established test sets that have been used to evaluate many other binding site prediction methods.
Availability:
FTSite is freely available as a web-based server at http://ftsite.bu.edu.
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