Moltiverse: Molecular Conformer Generation Using Enhanced Sampling Methods

Accurately predicting the diverse bound-state conformations of small molecules is crucial for successful drug discovery and design, particularly when detailed protein-ligand interactions are unknown. Established tools exist, but efficiently exploring the vast conformational space remains challenging. This work introduces Moltiverse, a novel protocol using enhanced sampling molecular dynamics (MD) simulations for conformer generation. The extended adaptive biasing force (eABF) algorithm combined with metadynamics, guided by a single collective variable (radius of gyration, RDGYR), efficiently samples the conformational landscape of a small molecule. Moltiverse demonstrates comparable accuracy and, in some cases, superior quality when benchmarked against established software like RDKit, CONFORGE, Balloon, iCon, and Conformator in the Platinum Diverse Data set for drug-like small molecules and the Prime data set for macrocycles. We present multiple quantitative metrics and statistical analysis for robust conformer generation algorithm comparisons and provide recommendations for their improvement based on our findings. Our extensive evaluation shows that Moltiverse is particularly effective for challenging systems with high conformational flexibility, such as macrocycles, where it achieves the highest accuracy among the tested algorithms. The physics-based approach employed by Moltiverse effectively handles a wide range of molecular complexities, positioning it as a valuable tool for computational drug discovery workflows requiring accurate representation of molecular flexibility.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2025-05-27
DOI
https://doi.org/10.1021/acs.jcim.5c00871
Citations
2
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
3.01

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article

Moltiverse: Molecular Conformer Generation Using Enhanced Sampling Methods

Wendy González, Leandro Martı́nez, José Carlos Estanislao Márquez Montesinos, Francisco Adasme‐Carreño et al.
2 citations
Journal of Chemical Information and Modeling
Computational Drug Discovery Methods
3.01
article

Moltiverse: Molecular Conformer Generation Using Enhanced Sampling Methods

Wendy González, Leandro Martı́nez, José Carlos Estanislao Márquez Montesinos, Francisco Adasme‐Carreño, Paula Andrea Peña-Martínez, Jans H. Alzate‐Morales, Erix W. Hernández‐Rodríguez, Mauricio Bedoya, Camila Muñoz‐Gutierrez, Luciano Peña-Tejo
article en
2 citations

Abstract

Accurately predicting the diverse bound-state conformations of small molecules is crucial for successful drug discovery and design, particularly when detailed protein-ligand interactions are unknown. Established tools exist, but efficiently exploring the vast conformational space remains challenging. This work introduces Moltiverse, a novel protocol using enhanced sampling molecular dynamics (MD) simulations for conformer generation. The extended adaptive biasing force (eABF) algorithm combined with metadynamics, guided by a single collective variable (radius of gyration, RDGYR), efficiently samples the conformational landscape of a small molecule. Moltiverse demonstrates comparable accuracy and, in some cases, superior quality when benchmarked against established software like RDKit, CONFORGE, Balloon, iCon, and Conformator in the Platinum Diverse Data set for drug-like small molecules and the Prime data set for macrocycles. We present multiple quantitative metrics and statistical analysis for robust conformer generation algorithm comparisons and provide recommendations for their improvement based on our findings. Our extensive evaluation shows that Moltiverse is particularly effective for challenging systems with high conformational flexibility, such as macrocycles, where it achieves the highest accuracy among the tested algorithms. The physics-based approach employed by Moltiverse effectively handles a wide range of molecular complexities, positioning it as a valuable tool for computational drug discovery workflows requiring accurate representation of molecular flexibility.

Journal of Chemical Information and ModelingVol. 65(12)
University of Talca (CL), Universidade Estadual de Campinas (UNICAMP) (BR), Catholic University of the Maule (CL)
Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação Amazônia Paraense de Amparo à Pesquisa, Agencia Nacional de Investigación y Desarrollo, Fondo Nacional de Desarrollo Científico y Tecnológico
Openalex Percentile: Top 9%
Computational Drug Discovery Methods
3.01
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