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3LOK

Drug resistant cSrc kinase domain in complex with covalent inhibitor PD168393

3LOK の概要
エントリーDOI10.2210/pdb3lok/pdb
関連するPDBエントリー2HWP 2QI8 2QLQ 2QQ7
分子名称Proto-oncogene tyrosine-protein kinase Src, N-[4-(3-BROMO-PHENYLAMINO)-QUINAZOLIN-6-YL]-ACRYLAMIDE (3 entities in total)
機能のキーワードsrc kinase domain, drug resistance, irreversible inhibitor, covalent inhibitor, pd168393, atp-binding, kinase, lipoprotein, myristate, nucleotide-binding, phosphoprotein, proto-oncogene, sh2 domain, sh3 domain, tyrosine-protein kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
由来する生物種Gallus gallus (chicken)
細胞内の位置Cell membrane (By similarity): P00523
タンパク質・核酸の鎖数2
化学式量合計66284.03
構造登録者
Gruetter, C.,Rode, H.B.,Rauh, D. (登録日: 2010-02-04, 公開日: 2010-12-22, 最終更新日: 2023-11-01)
主引用文献Klueter, S.,Simard, J.R.,Rode, H.B.,Gruetter, C.,Pawar, V.,Raaijmakers, H.C.,Barf, T.A.,Rabiller, M.,van Otterlo, W.A.L.,Rauh, D.
Characterization of irreversible kinase inhibitors by directly detecting covalent bond formation: a tool for dissecting kinase drug resistance
Chembiochem, 11:2557-2566, 2010
Cited by
PubMed: 21080395
DOI: 10.1002/cbic.201000352
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.48 Å)
構造検証レポート
Validation report summary of 3lok
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2024-06-12に公開中

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