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3Q6S

The crystal structure of the heterochromatin protein 1 beta chromoshadow domain complexed with a peptide from Shugoshin 1

3Q6S の概要
エントリーDOI10.2210/pdb3q6s/pdb
分子名称Chromobox protein homolog 1, Shugoshin-like 1 (3 entities in total)
機能のキーワードincenp, heterochromatin, centromere, cell cycle
由来する生物種Homo sapiens (human)
詳細
細胞内の位置Nucleus: P83916 Q5FBB7
タンパク質・核酸の鎖数6
化学式量合計40241.21
構造登録者
Brautigam, C.A.,Chaudhary, J.,Yu, H. (登録日: 2011-01-03, 公開日: 2011-12-14, 最終更新日: 2024-02-21)
主引用文献Kang, J.,Chaudhary, J.,Dong, H.,Kim, S.,Brautigam, C.A.,Yu, H.
Mitotic centromeric targeting of HP1 and its binding to Sgo1 are dispensable for sister-chromatid cohesion in human cells.
Mol Biol Cell, 22:1181-1190, 2011
Cited by
PubMed Abstract: Human Shugoshin 1 (Sgo1) protects centromeric sister-chromatid cohesion during prophase and prevents premature sister-chromatid separation. Heterochromatin protein 1 (HP1) has been proposed to protect centromeric sister-chromatid cohesion by directly targeting Sgo1 to centromeres in mitosis. Here we show that HP1α is targeted to mitotic centromeres by INCENP, a subunit of the chromosome passenger complex (CPC). Biochemical and structural studies show that both HP1-INCENP and HP1-Sgo1 interactions require the binding of the HP1 chromo shadow domain to PXVXL/I motifs in INCENP or Sgo1, suggesting that the INCENP-bound, centromeric HP1α is incapable of recruiting Sgo1. Consistently, a Sgo1 mutant deficient in HP1 binding is functional in centromeric cohesion protection and localizes normally to centromeres in mitosis. By contrast, INCENP or Sgo1 mutants deficient in HP1 binding fail to localize to centromeres in interphase. Therefore, our results suggest that HP1 binding by INCENP or Sgo1 is dispensable for centromeric cohesion protection during mitosis of human cells, but might regulate yet uncharacterized interphase functions of CPC or Sgo1 at the centromeres.
PubMed: 21346195
DOI: 10.1091/mbc.E11-01-0009
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.93 Å)
構造検証レポート
Validation report summary of 3q6s
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2026-04-22に公開中

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