4R8Q

Structure and substrate recruitment of the human spindle checkpoint kinase bub1

「3E7E」から置き換えられました

4R8Q の概要

• エントリーDOI: 10.2210/pdb4r8q/pdb
• 関連するPDBエントリー: 4QPM
• 分子名称: Mitotic checkpoint serine/threonine-protein kinase BUB1, ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... (4 entities in total)
• 機能のキーワード: spindle assembly checkpoint, mitosis, kinase, activation, ken box, cdc20, atp-binding, cell cycle, cell division, disease mutation, nucleotide-binding, nucleus, phosphoprotein, serine/threonine-protein kinase, transferase
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Nucleus: O43683
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 42323.39

構造登録者

Tomchick, D.R.,Yu, H. (登録日: 2014-09-02, 公開日: 2014-11-12, 最終更新日: 2024-02-28)

主引用文献

Kang, J.,Yang, M.,Li, B.,Qi, W.,Zhang, C.,Shokat, K.M.,Tomchick, D.R.,Machius, M.,Yu, H.
Structure and substrate recruitment of the human spindle checkpoint kinase Bub1.
Mol.Cell, 32:394-405, 2008

PubMed Abstract: In mitosis, the spindle checkpoint detects a single unattached kinetochore, inhibits the anaphase-promoting complex or cyclosome (APC/C), and prevents premature sister chromatid separation. The checkpoint kinase Bub1 contributes to checkpoint sensitivity through phosphorylating the APC/C activator, Cdc20, and inhibiting APC/C catalytically. We report here the crystal structure of the kinase domain of Bub1, revealing the requirement of an N-terminal extension for its kinase activity. Though the activation segment of Bub1 is ordered and has structural features indicative of active kinases, the C-terminal portion of this segment sterically restricts substrate access to the active site. Bub1 uses docking motifs, so-called KEN boxes, outside its kinase domain to recruit Cdc20, one of two known KEN box receptors. The KEN boxes of Bub1 are required for the spindle checkpoint in human cells. Therefore, its unusual active-site conformation and mode of substrate recruitment suggest that Bub1 has an exquisitely tuned specificity for Cdc20.

PubMed: 18995837
DOI: 10.1016/j.molcel.2008.09.017

実験手法

X-RAY DIFFRACTION (2.31 Å)