2BFY
Complex of Aurora-B with INCENP and Hesperadin.
2BFY の概要
| エントリーDOI | 10.2210/pdb2bfy/pdb |
| 関連するPDBエントリー | 2BFX |
| 分子名称 | AURORA KINASE B-A, INNER CENTROMERE PROTEIN A, N-[2-OXO-3-((E)-PHENYL{[4-(PIPERIDIN-1-YLMETHYL)PHENYL]IMINO}METHYL)-2,6-DIHYDRO-1H-INDOL-5-YL]ETHANESULFONAMIDE, ... (4 entities in total) |
| 機能のキーワード | transferase, kinase, mitosis, inhibition, transferase complex |
| 由来する生物種 | XENOPUS LAEVIS (AFRICAN CLAWED FROG) 詳細 |
| 細胞内の位置 | Nucleus: Q6DE08 Chromosome, centromere: O13024 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 78146.49 |
| 構造登録者 | Sessa, F.,Mapelli, M.,Ciferri, C.,Tarricone, C.,Areces, L.B.,Schneider, T.R.,Stukenberg, P.T.,Musacchio, A. (登録日: 2004-12-15, 公開日: 2005-05-03, 最終更新日: 2024-11-06) |
| 主引用文献 | Sessa, F.,Mapelli, M.,Ciferri, C.,Tarricone, C.,Areces, L.B.,Schneider, T.R.,Stukenberg, P.T.,Musacchio, A. Mechanism of Aurora B Activation by Incenp and Inhibition by Hesperadin Mol.Cell, 18:379-, 2005 Cited by PubMed Abstract: Aurora family serine/threonine kinases control mitotic progression, and their deregulation is implicated in tumorigenesis. Aurora A and Aurora B, the best-characterized members of mammalian Aurora kinases, are approximately 60% identical but bind to unrelated activating subunits. The structure of the complex of Aurora A with the TPX2 activator has been reported previously. Here, we report the crystal structure of Aurora B in complex with the IN-box segment of the inner centromere protein (INCENP) activator and with the small molecule inhibitor Hesperadin. The Aurora B:INCENP complex is remarkably different from the Aurora A:TPX2 complex. INCENP forms a crown around the small lobe of Aurora B and induces the active conformation of the T loop allosterically. The structure represents an intermediate state of activation of Aurora B in which the Aurora B C-terminal segment stabilizes an open conformation of the catalytic cleft, and a critical ion pair in the kinase active site is impaired. Phosphorylation of two serines in the carboxyl terminus of INCENP generates the fully active kinase. PubMed: 15866179DOI: 10.1016/J.MOLCEL.2005.03.031 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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