<i>fpocketR</i> : A Platform for Identification and Analysis of Ligand-Binding Pockets in RNA

Small molecules that bind specific sites in RNAs hold promise for altering RNA function, manipulating gene expression, and expanding the scope of druggable targets beyond proteins. Identifying binding sites in RNA that can engage ligands with good physicochemical properties remains a significant challenge. <i>fpocketR</i> is a software and framework for identifying, characterizing, and visualizing ligand-binding sites in RNA. <i>fpocketR</i> was optimized, through a comprehensive analysis of currently available RNA-ligand complexes, to identify pockets in RNAs able to bind small molecules possessing favorable properties, generally termed drug-like. Here, we demonstrate multiple, complex, uses of <i>fpocketR</i> to analyze RNA-ligand interactions and novel pockets in small and large RNAs, to assess ensembles of RNA structure models, to identify pockets in dynamic RNA systems, and to evaluate the shapes of RNA pockets. <i>fpocketR</i> performs best with RNA structures visualized at atomistic resolution but also provides useful information with lower resolution structures and computational models. <i>fpocketR</i> is a powerful, ligand-agnostic tool for discovery and analysis of targetable pockets in RNA molecules.

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Publication Details

Journal
ACS Chemical Biology
Published
2025-12-17
DOI
https://doi.org/10.1021/acschembio.5c00805
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

fpocketR : A Platform for Identification and Analysis of Ligand-Binding Pockets in RNA

Simon Felder, Seth D. Veenbaas, Kevin M. Weeks
ACS Chemical Biology
RNA and protein synthesis mechanisms
article

fpocketR : A Platform for Identification and Analysis of Ligand-Binding Pockets in RNA

Simon Felder, Seth D. Veenbaas, Kevin M. Weeks
article en

Abstract

Small molecules that bind specific sites in RNAs hold promise for altering RNA function, manipulating gene expression, and expanding the scope of druggable targets beyond proteins. Identifying binding sites in RNA that can engage ligands with good physicochemical properties remains a significant challenge. <i>fpocketR</i> is a software and framework for identifying, characterizing, and visualizing ligand-binding sites in RNA. <i>fpocketR</i> was optimized, through a comprehensive analysis of currently available RNA-ligand complexes, to identify pockets in RNAs able to bind small molecules possessing favorable properties, generally termed drug-like. Here, we demonstrate multiple, complex, uses of <i>fpocketR</i> to analyze RNA-ligand interactions and novel pockets in small and large RNAs, to assess ensembles of RNA structure models, to identify pockets in dynamic RNA systems, and to evaluate the shapes of RNA pockets. <i>fpocketR</i> performs best with RNA structures visualized at atomistic resolution but also provides useful information with lower resolution structures and computational models. <i>fpocketR</i> is a powerful, ligand-agnostic tool for discovery and analysis of targetable pockets in RNA molecules.

ACS Chemical BiologyVol. 21(1)
University of North Carolina at Chapel Hill (US)
Openalex Percentile: Top 63%
RNA and protein synthesis mechanisms
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