SiDGen: Structure-informed Diffusion for Generative modeling of Ligands for Proteins

Structure-based drug design (SBDD) faces a fundamental scaling fidelity dilemma: rich pocket-aware conditioning captures interaction geometry but can be costly, often scales quadratically (O(L2)) or worse with protein length (L), while efficient sequence-only conditioning can miss key interaction structure. We propose SiDGen, a structure-informed discrete diffusion framework that resolves this trade-off through a Topological Information Bottleneck (TIB). SiDGen leverages a learned, soft assignment mechanism to compress residue-level protein representations into a compact bottleneck enabling downstream pairwise computations on the coarse grid (O(L2/s2)). This design reduces memory and computational cost without compromising generative accuracy. Our approach achieves state-of-the-art performance on CrossDocked2020 and DUD-E benchmarks while significantly reducing pairwise-tensor memory. SiDGen bridges the gap between sequence-based efficiency and pocket-aware conditioning, offering a scalable path for high-throughput structure-based discovery.