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4CA0

Structural Basis for the microtubule binding of the human kinetochore Ska complex

4CA0 の概要
エントリーDOI10.2210/pdb4ca0/pdb
関連するPDBエントリー4C9Y
分子名称SPINDLE AND KINETOCHORE-ASSOCIATED PROTEIN 1 (2 entities in total)
機能のキーワードcell cycle, cell divison, kinetochore-microtubule attachment, winged-helix domain
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Cytoplasm, cytoskeleton, spindle: Q96BD8
タンパク質・核酸の鎖数2
化学式量合計29288.22
構造登録者
主引用文献Abad, M.A.,Medina, B.,Santamaria, A.,Zou, J.,Plasberg-Hill, C.,Madhumalar, A.,Jayachandran, U.,Redli, P.M.,Rappsilber, J.,Nigg, E.A.,Jeyaprakash, A.A.
Structural Basis for Microtubule Recognition by the Human Kinetochore Ska Complex.
Nat.Commun., 5:2964-, 2014
Cited by
PubMed Abstract: The ability of kinetochores (KTs) to maintain stable attachments to dynamic microtubule structures ('straight' during microtubule polymerization and 'curved' during microtubule depolymerization) is an essential requirement for accurate chromosome segregation. Here we show that the kinetochore-associated Ska complex interacts with tubulin monomers via the carboxy-terminal winged-helix domain of Ska1, providing the structural basis for the ability to bind both straight and curved microtubule structures. This contrasts with the Ndc80 complex, which binds straight microtubules by recognizing the dimeric interface of tubulin. The Ska1 microtubule-binding domain interacts with tubulins using multiple contact sites that allow the Ska complex to bind microtubules in multiple modes. Disrupting either the flexibility or the tubulin contact sites of the Ska1 microtubule-binding domain perturbs normal mitotic progression, explaining the critical role of the Ska complex in maintaining a firm grip on dynamic microtubules.
PubMed: 24413531
DOI: 10.1038/NCOMMS3964
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.259 Å)
構造検証レポート
Validation report summary of 4ca0
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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