EC-Conf: A ultra-fast diffusion model for molecular conformation generation with equivariant consistency
Despite recent advancement in 3D molecule conformation generation driven by diffusion models, its high computational cost in iterative diffusion/denoising process limits its application. Here, an equivariant consistency model (EC-Conf) was proposed as a fast diffusion method for low-energy conformation generation. In EC-Conf, a modified SE (3)-equivariant transformer model was directly used to encode the Cartesian molecular conformations and a highly efficient consistency diffusion process was carried out to generate molecular conformations. It was demonstrated that, with only one sampling step, it can already achieve comparable quality to other diffusion-based models running with thousands denoising steps. Its performance can be further improved with a few more sampling iterations. The performance of EC-Conf is evaluated on both GEOM-QM9 and GEOM-Drugs sets. Our results demonstrate that the efficiency of EC-Conf for learning the distribution of low energy molecular conformation is at least two magnitudes higher than current SOTA diffusion models and could potentially become a useful tool for conformation generation and sampling. SCIENTIFIC CONTRIBUTIONS: In this work, we proposed an equivariant consistency model that significantly improves the efficiency of conformation generation in diffusion-based models while maintaining high structural quality. This method serves as a general framework and can be further extended to more complex structure generation and prediction tasks, including those involving proteins, in future steps.
Authors
- Mingyuan Xu (ORCID: https://orcid.org/0000-0003-0463-4249)
- Yuedong Yang (ORCID: https://orcid.org/0000-0002-6782-2813)
- Hongming Chen (ORCID: https://orcid.org/0000-0002-4470-876X)
- Zhiguang Fan
Institutions
- Sun Yat-sen University (CN)
Publication Details
- Journal
- Journal of Cheminformatics
- Published
- 2024-09-03
- DOI
- https://doi.org/10.1186/s13321-024-00893-2
- Citations
- 7
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 2.53
Funders
- Guangdong Provincial Pearl River Talents Program