9MAT
TopBP1 BRCT 7-8 Domain
Summary for 9MAT
| Entry DOI | 10.2210/pdb9mat/pdb |
| Descriptor | DNA topoisomerase 2-binding protein 1, MALONIC ACID (3 entities in total) |
| Functional Keywords | dna topoisomerase 2-binding protein 1, isomerase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 26490.29 |
| Authors | |
| Primary citation | Chen, W.,Zhang, S.,Li, Z.,Wang, L.,Zhang, J.,Gao, J.,Ruan, K. Fragment-based discovery of TopBP1 inhibitors integrated with AI-driven molecular docking. Magn Reson Lett, 6:200251-200251, 2026 Cited by PubMed Abstract: DNA topoisomerase IIβ-binding protein 1 (TopBP1) converges on multiple oncogenic pathways, e.g., Rb, p53, and PI3K/Akt, which are hallmarks of most cancer progression. However, the lack of structural studies makes the underlying mechanism of action of TopBP1 inhibitors promiscuous. Herein, we employ a fragment-based screening approach to identify four small-molecule ligands against the TopBP1 BRCT7-8 domain: adamantane acetic acid (ADA), zaltoprofen, diclofenac sodium, and quinine. The dissociation constants of these compounds are determined by nuclear magnetic resonance (NMR) chemical shift perturbations, which suggests the former three hits bind to the same site, while quinine binds to a distinct site. The binding models of these four hits are further predicted by the deep learning model Chai-1. The complex crystal structure of the TopBP1 BRCT7-8 domain demonstrates ADA as an orthosteric inhibitor of TopBP1, as further validated by its binding to TopBP1 in competition with the native substrate BACH1. Our NMR screening nominates orthosteric inhibitors, as well as quinine, a potential allosteric inhibitor. It shall also facilitate following structure-based design of more potent allosteric and orthosteric inhibitors of TopBP1. PubMed: 42221021DOI: 10.1016/j.mrl.2025.200251 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.65 Å) |
Structure validation
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