Abstract
We present the structure of the human Aurora B kinase domain in complex with the C-terminal Aurora-binding region of human INCENP and the Aurora kinase inhibitor VX-680. The structure unexpectedly reveals a dimeric arrangement of the Aurora B:INCENP complex, which was confirmed to exist in solution by analytical ultracentrifugation. The dimerization involves a domain swap of the activation loop, resulting in a different conformation of the DFG motif as compared to that seen in other kinase complexes with VX-680. The binding of INCENP differs significantly from that seen in the Xenopus laevis Aurora B:INCENP complex currently used as a model for structure-based design for this important oncology target. © 2012 American Chemical Society.
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CITATION STYLE
Elkins, J. M., Santaguida, S., Musacchio, A., & Knapp, S. (2012). Crystal structure of human aurora B in complex with INCENP and VX-680. Journal of Medicinal Chemistry, 55(17), 7841–7848. https://doi.org/10.1021/jm3008954
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