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4R8Q

Structure and substrate recruitment of the human spindle checkpoint kinase bub1

Replaces:  3E7E
Summary for 4R8Q
Entry DOI10.2210/pdb4r8q/pdb
Related4QPM
DescriptorMitotic checkpoint serine/threonine-protein kinase BUB1, ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordsspindle 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
Biological sourceHomo sapiens (human)
Cellular locationNucleus: O43683
Total number of polymer chains1
Total formula weight42323.39
Authors
Tomchick, D.R.,Yu, H. (deposition date: 2014-09-02, release date: 2014-11-12, Last modification date: 2024-02-28)
Primary citationKang, 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
Cited by
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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.31 Å)
Structure validation

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