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9IMO

Crystal structure of Tubulin-RB3-TTL-Y12

This is a non-PDB format compatible entry.
Summary for 9IMO
Entry DOI10.2210/pdb9imo/pdb
DescriptorTubulin alpha-1B chain, PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER, Tubulin beta chain, ... (11 entities in total)
Functional Keywordstubulin, cell cycle
Biological sourceRattus norvegicus (Norway rat)
More
Total number of polymer chains6
Total formula weight267628.53
Authors
Yan, W.,Yang, J.H. (deposition date: 2024-07-04, release date: 2025-02-26, Last modification date: 2025-03-26)
Primary citationLi, Y.,Zhang, C.,Tang, D.,Wang, T.,Yan, W.,Yang, L.,Bai, P.,Tang, M.,Pei, H.,Chen, L.,Chen, Q.,Yang, J.
Identification of a ligand-binding site on tubulin mediating the tubulin-RB3 interaction.
Proc.Natl.Acad.Sci.USA, 122:e2424098122-e2424098122, 2025
Cited by
PubMed Abstract: For decades, microtubules-composed of αβ-tubulin dimers-have been primary targets for cancer chemotherapy. While eight binding sites on the tubulin dimer have been structurally characterized, this study reveals a ninth. We found that the tubulin inhibitor Tumabulin-1 (TM1, a BML284 derivative) binds simultaneously to the well-known colchicine site and a previously unknown site, designated as Tumabulin site. This site resides at the interface of α1-tubulin, β1-tubulin, and RB3 within the tubulin-RB3-tubulintyrosine ligase complex. Remarkably, two TM1 molecules bind cooperatively to this relatively large pocket, interacting with all three proteins. Crucially, this binding is dependent on RB3; it is absent when RB3 is missing or the key residue H71 is mutated (H71Q). We further designed and synthesized Tumabulin-2 (TM2) that selectively binds the Tumabulin site, excluding binding the colchicine site. TM2 acts as a molecular glue, strengthening the interaction between RB3 and the tubulin dimer and consequently enhancing RB3's tubulin-depolymerizing activity. In conclusion, our findings confirm the existence of a ninth tubulin-binding site and offer a promising foundation for developing Tubulin-RB3 molecular glues as a next generation of anticancer therapeutics.
PubMed: 40067895
DOI: 10.1073/pnas.2424098122
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.75 Å)
Structure validation

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