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Crystal Structure of Human Aurora B in Complex with INCENP and VX-680

[Image: see text] 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...

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Autores principales: Elkins, Jonathan M., Santaguida, Stefano, Musacchio, Andrea, Knapp, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621106/
https://www.ncbi.nlm.nih.gov/pubmed/22920039
http://dx.doi.org/10.1021/jm3008954
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author Elkins, Jonathan M.
Santaguida, Stefano
Musacchio, Andrea
Knapp, Stefan
author_facet Elkins, Jonathan M.
Santaguida, Stefano
Musacchio, Andrea
Knapp, Stefan
author_sort Elkins, Jonathan M.
collection PubMed
description [Image: see text] 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.
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spelling pubmed-36211062013-04-09 Crystal Structure of Human Aurora B in Complex with INCENP and VX-680 Elkins, Jonathan M. Santaguida, Stefano Musacchio, Andrea Knapp, Stefan J Med Chem [Image: see text] 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. American Chemical Society 2012-08-27 2012-09-13 /pmc/articles/PMC3621106/ /pubmed/22920039 http://dx.doi.org/10.1021/jm3008954 Text en Copyright © 2012 American Chemical Society
spellingShingle Elkins, Jonathan M.
Santaguida, Stefano
Musacchio, Andrea
Knapp, Stefan
Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title_full Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title_fullStr Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title_full_unstemmed Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title_short Crystal Structure of Human Aurora B in Complex with INCENP and VX-680
title_sort crystal structure of human aurora b in complex with incenp and vx-680
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621106/
https://www.ncbi.nlm.nih.gov/pubmed/22920039
http://dx.doi.org/10.1021/jm3008954
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