4DZO

Structure of Human Mad1 C-terminal Domain Reveals Its Involvement in Kinetochore Targeting

4DZO の概要

• エントリーDOI: 10.2210/pdb4dzo/pdb
• 分子名称: Mitotic spindle assembly checkpoint protein MAD1 (2 entities in total)
• 機能のキーワード: homodimer, kinetochore, mitosis, spindle checkpoint protein, mad2, nucleus, cell cycle
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Nucleus: Q9Y6D9
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 28131.56

構造登録者

Luo, X.,Sun, H.,Tomchick, D.R. (登録日: 2012-03-01, 公開日: 2012-04-11, 最終更新日: 2024-11-20)

主引用文献

Kim, S.,Sun, H.,Tomchick, D.R.,Yu, H.,Luo, X.
Structure of human Mad1 C-terminal domain reveals its involvement in kinetochore targeting.
Proc.Natl.Acad.Sci.USA, 109:6549-6554, 2012

PubMed Abstract: The spindle checkpoint prevents aneuploidy by delaying anaphase onset until all sister chromatids achieve proper microtubule attachment. The kinetochore-bound checkpoint protein complex Mad1-Mad2 promotes the conformational activation of Mad2 and serves as a catalytic engine of checkpoint signaling. How Mad1 is targeted to kinetochores is not understood. Here, we report the crystal structure of the conserved C-terminal domain (CTD) of human Mad1. Mad1 CTD forms a homodimer and, unexpectedly, has a fold similar to those of the kinetochore-binding domains of Spc25 and Csm1. Nonoverlapping Mad1 fragments retain detectable kinetochore targeting. Deletion of the CTD diminishes, does not abolish, Mad1 kinetochore localization. Mutagenesis studies further map the functional interface of Mad1 CTD in kinetochore targeting and implicate Bub1 as its receptor. Our results indicate that CTD is a part of an extensive kinetochore-binding interface of Mad1, and rationalize graded kinetochore targeting of Mad1 during checkpoint signaling.

PubMed: 22493223
DOI: 10.1073/pnas.1118210109

実験手法

X-RAY DIFFRACTION (1.76 Å)