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Equivariant Blurring Diffusion for Hierarchical Molecular Conformer Generation

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arxiv 2410.20255 v1 pith:XWR6LCDB submitted 2024-10-26 cs.LG cs.AIphysics.chem-phq-bio.BM

Equivariant Blurring Diffusion for Hierarchical Molecular Conformer Generation

classification cs.LG cs.AIphysics.chem-phq-bio.BM
keywords coarse-graineddiffusionmolecularprocessblurringequivariantgenerationstructure
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
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How can diffusion models process 3D geometries in a coarse-to-fine manner, akin to our multiscale view of the world? In this paper, we address the question by focusing on a fundamental biochemical problem of generating 3D molecular conformers conditioned on molecular graphs in a multiscale manner. Our approach consists of two hierarchical stages: i) generation of coarse-grained fragment-level 3D structure from the molecular graph, and ii) generation of fine atomic details from the coarse-grained approximated structure while allowing the latter to be adjusted simultaneously. For the challenging second stage, which demands preserving coarse-grained information while ensuring SE(3) equivariance, we introduce a novel generative model termed Equivariant Blurring Diffusion (EBD), which defines a forward process that moves towards the fragment-level coarse-grained structure by blurring the fine atomic details of conformers, and a reverse process that performs the opposite operation using equivariant networks. We demonstrate the effectiveness of EBD by geometric and chemical comparison to state-of-the-art denoising diffusion models on a benchmark of drug-like molecules. Ablation studies draw insights on the design of EBD by thoroughly analyzing its architecture, which includes the design of the loss function and the data corruption process. Codes are released at https://github.com/Shen-Lab/EBD .

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  1. Align Your Structures: Generating Trajectories with Structure Pretraining for Molecular Dynamics

    cs.LG 2026-04 conditional novelty 6.5

    Structure-pretrained diffusion plus an equivariant temporal interpolator generates chemically realistic MD trajectories on small molecules, tetrapeptides, and proteins by separating spatial and temporal learning.