Crystal structure of ITK in complex with compound 7 [4-(carbamoylamino)-1-(7-ethoxynaphthalen-1-yl)-1H-pyrazole-3-carboxamide]
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Crystal structure of ITK in complex with compound 7 [4-(carbamoylamino)-1-(7-ethoxynaphthalen-1-yl)-1H-pyrazole-3-carboxamide] Descriptor: 4-(carbamoylamino)-1-(7-ethoxynaphthalen-1-yl)-1H-pyrazole-3-carboxamide, Tyrosine-protein kinase ITK/TSK Authors: Han, S, Caspers, N.L. Deposit date: 2013-08-02 Release date: 2014-04-02 Last modified: 2024-02-28 Method: X-RAY DIFFRACTION (2.15 Å) Cite: Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors. Biochem.J., 460, 2014
与化合物7 [4-(氨基甲酰氨基)-1-(7-乙氧基萘-1-基)-1H-吡唑-3-甲酰胺]结合的ITK晶体结构
描述物:4-(氨基甲酰氨基)-1-(7-乙氧基萘-1-基)-1H-吡唑-3-甲酰胺、酪氨酸蛋白激酶ITK/TSK(Tyrosine-protein kinase ITK/TSK)
作者:Han, S.、Caspers, N.L.
提交日期:2013-08-02
发布日期:2014-04-02
末次修改日期:2024-02-28
实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率2.15埃(Å)
引用文献:《通过变构抑制剂选择性靶向白细胞介素-2诱导性T细胞激酶的非活性构象》,《生物化学期刊(Biochem.J.)》,第460卷,2014年
创建时间:
2013-08-02



