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ADT addresses a critical bottleneck in 3D molecular generation by decoupling token granularity from reconstruction resolution, allowing discrete autoregressive models to recover fine-grained atomic geometry without prohibitive sequence lengths. By leveraging diffusion models to correct quantization artifacts, this method enables high-quality generation of both small molecules and protein structures while maintaining compact representations. This advancement significantly improves the efficiency and fidelity of AI-driven drug discovery pipelines that rely on all-atom structural data.
ADT: All-Atom Diffusion Tokenizer for 3D Molecular Structures
arXiv:2610.23265v1 Announce Type: new Abstract: Discrete structural tokenization provides a promising route to autoregressive 3D molecular generation. Yet, existing tokenizers face a trade-off between compact representation and all-atom reconstruction: atom-level tokens preserve atomic details but produce long sequences, while compact residue-level protein tokens typically omit side-chain geometry. To overcome this limitation, we propose All-atom Diffusion Tokenizer (ADT), which decouples token granularity from reconstruction resolution. ADT uses one structural token per atom for small molecules and one token per protein residue that jointly represents backbone and side-chain geometry. To mitigate geometric distortion introduced by quantization, we leverage the generative capacity of diffusion models to recover fine-grained atomic geometry beyond deterministic decoding from discrete tokens. Extensive experiments across small molecules and proteins demonstrate that ADT achieves strong reconstruction from compact discrete representations while enabling high-quality autoregressive generation of both small molecules and all-atom protein structures. These results establish compact structural tokens as an effective discrete interface for all-atom molecular reconstruction and generation.
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