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1OPJ

Structural basis for the auto-inhibition of c-Abl tyrosine kinase

1OPJ の概要
エントリーDOI10.2210/pdb1opj/pdb
関連するPDBエントリー1OPK 1OPL
分子名称Proto-oncogene tyrosine-protein kinase ABL1, CHLORIDE ION, MYRISTIC ACID, ... (5 entities in total)
機能のキーワードtransferase
由来する生物種Mus musculus (house mouse)
細胞内の位置Cytoplasm, cytoskeleton: P00520
タンパク質・核酸の鎖数2
化学式量合計69001.90
構造登録者
Nagar, B.,Hantschel, O.,Young, M.A.,Scheffzek, K.,Veach, D.,Bornmann, W.,Clarkson, B.,Superti-Furga, G.,Kuriyan, J. (登録日: 2003-03-06, 公開日: 2003-04-08, 最終更新日: 2024-03-13)
主引用文献Nagar, B.,Hantschel, O.,Young, M.A.,Scheffzek, K.,Veach, D.,Bornmann, W.,Clarkson, B.,Superti-Furga, G.,Kuriyan, J.
Structural basis for the autoinhibition of c-Abl tyrosine kinase
Cell(Cambridge,Mass.), 112:859-871, 2003
Cited by
PubMed Abstract: c-Abl is normally regulated by an autoinhibitory mechanism, the disruption of which leads to chronic myelogenous leukemia. The details of this mechanism have been elusive because c-Abl lacks a phosphotyrosine residue that triggers the assembly of the autoinhibited form of the closely related Src kinases by internally engaging the SH2 domain. Crystal structures of c-Abl show that the N-terminal myristoyl modification of c-Abl 1b binds to the kinase domain and induces conformational changes that allow the SH2 and SH3 domains to dock onto it. Autoinhibited c-Abl forms an assembly that is strikingly similar to that of inactive Src kinases but with specific differences that explain the differential ability of the drug STI-571/Gleevec/imatinib (STI-571) to inhibit the catalytic activity of Abl, but not that of c-Src.
PubMed: 12654251
DOI: 10.1016/S0092-8674(03)00194-6
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.75 Å)
構造検証レポート
Validation report summary of 1opj
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2025-12-31に公開中

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