Multi-domain Distribution Learning for De Novo Drug Design
Reviewed by Pithpith:KT7AZWBMopen to challenge →
read the original abstract
We introduce DrugFlow, a generative model for structure-based drug design that integrates continuous flow matching with discrete Markov bridges, demonstrating state-of-the-art performance in learning chemical, geometric, and physical aspects of three-dimensional protein-ligand data. We endow DrugFlow with an uncertainty estimate that is able to detect out-of-distribution samples. To further enhance the sampling process towards distribution regions with desirable metric values, we propose a joint preference alignment scheme applicable to both flow matching and Markov bridge frameworks. Furthermore, we extend our model to also explore the conformational landscape of the protein by jointly sampling side chain angles and molecules.
This paper has not been read by Pith yet.
Forward citations
Cited by 1 Pith paper
-
Demystifying Multimodal Biomolecular Co-design With Intrinsic Geodesic Coupling
GeoCoupling optimizes temporal couplings between modalities in biomolecular generative models and outperforms synchronous baselines on drug design and protein design tasks.
discussion (0)
Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.