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3S4Z

Structure of a Y DNA-FANCI complex

3S4Z の概要
エントリーDOI10.2210/pdb3s4z/pdb
分子名称dna repair 1 (1 entity in total)
機能のキーワードdna repair, dna binding protein
由来する生物種Mus musculus (mouse)
細胞内の位置Nucleus (By similarity): Q8K368
タンパク質・核酸の鎖数3
化学式量合計441361.69
構造登録者
Pavletich, N.P. (登録日: 2011-05-20, 公開日: 2011-07-27, 最終更新日: 2024-02-28)
主引用文献Joo, W.,Xu, G.,Persky, N.S.,Smogorzewska, A.,Rudge, D.G.,Buzovetsky, O.,Elledge, S.J.,Pavletich, N.P.
Structure of the FANCI-FANCD2 complex: insights into the Fanconi anemia DNA repair pathway.
Science, 333:312-316, 2011
Cited by
PubMed Abstract: Fanconi anemia is a cancer predisposition syndrome caused by defects in the repair of DNA interstrand cross-links (ICLs). Central to this pathway is the Fanconi anemia I-Fanconi anemia D2 (FANCI-FANCD2) (ID) complex, which is activated by DNA damage-induced phosphorylation and monoubiquitination. The 3.4 angstrom crystal structure of the ~300 kilodalton ID complex reveals that monoubiquitination and regulatory phosphorylation sites map to the I-D interface, suggesting that they occur on monomeric proteins or an opened-up complex and that they may serve to stabilize I-D heterodimerization. The 7.8 angstrom electron-density map of FANCI-DNA crystals and in vitro data show that each protein has binding sites for both single- and double-stranded DNA, suggesting that the ID complex recognizes DNA structures that result from the encounter of replication forks with an ICL.
PubMed: 21764741
DOI: 10.1126/science.1205805
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (7.8 Å)
構造検証レポート
Validation report summary of 3s4z
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2025-07-16に公開中

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