3LOK
Drug resistant cSrc kinase domain in complex with covalent inhibitor PD168393
3LOK の概要
エントリーDOI | 10.2210/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 | |
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: 21080395DOI: 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
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