Deep Learning for Protein Complex Prediction and Design
About
Accurately modeling and designing protein complex structures is a central problem in computational structural biology, with broad implications for understanding cellular function and developing therapeutics. This thesis investigates two fundamental aspects of this problem using deep learning: domain-specific architectures that capture the hierarchical nature of protein structures, and search algorithms that efficiently navigate the vast sequence spaces of protein complexes to identify interacting homologs for improving complex structure prediction and to design protein sequences.
Ziwei Xie• 2026
Related benchmarks
| Task | Dataset | Result | Rank | |
|---|---|---|---|---|
| Binding affinity prediction | SKEMPI v2.0 | Spearman ρ0.28 | 30 | |
| Protein Sequence Recovery | Monomer | NSR0.43 | 11 | |
| Protein Sequence Recovery | Homodimer | NSR49 | 11 | |
| Protein Sequence Recovery | Heterodimer | NSR43 | 11 | |
| Interfacial contact prediction | HomoPDB PDB2018 (test) | Top-10 Precision48 | 6 | |
| Heterodimer self-consistency | Heterodimer 107 targets | Success Rate (SR)30 | 6 | |
| Heterodimer structure prediction | pConf70 (test) | Top 5 Best DockQ Score0.259 | 4 | |
| Heterodimer structure prediction | DockQ49 (test) | Top 5 DockQ Score0.265 | 4 | |
| Heterodimer structure prediction | pConf80 (test) | Top 5 DockQ0.423 | 4 | |
| Interfacial contact prediction | HomoCASP CASP-CAPRI | Top-10 Precision54 | 4 |
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