| タイトル | Crystal structure of the cdk2 in complex with aminopyrazole inhibitor |
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| ジャーナル・号・ページ | To be Published |
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| 掲載日 | 2012年4月9日 (構造データの登録日) |
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著者 | Kang, Y.N. / Stuckey, J.A. |
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リンク | PubMedで検索 |
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| 手法 | X線回折 |
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| 解像度 | 1.26 - 1.63 Å |
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| 構造データ | PDB-4ek4: Crystal structure of the cdk2 in complex with aminopyrazole inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.26 Å PDB-4ek5: Crystal structure of the cdk2 in complex with aminopyrazole inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.6 Å PDB-4ek6: Crystal structure of the cdk2 in complex with aminopyrazole inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.52 Å PDB-4fkg: Crystal structure of the cdk2 in complex with aminopyrazole inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.51 Å PDB-4fkj: Crystal structure of the cdk2 in complex with aminopyrazole inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.63 Å |
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| 化合物 | ChemComp-1CK: 4-bromo-N-(5-methyl-1H-pyrazol-3-yl)benzamide
ChemComp-03K: N-(5-cyclopropyl-1H-pyrazol-3-yl)benzene-1,4-dicarboxamide
ChemComp-10K: N-(3-cyclopropyl-1H-pyrazol-5-yl)-2-[4-(thiophen-2-yl)phenyl]acetamide
ChemComp-4CK: 4-[(5-cyclopropyl-1H-pyrazol-3-yl)carbamoyl]benzoic acid
ChemComp-11K: N-(3-cyclopropyl-1H-pyrazol-5-yl)-2-[4-(2-pyrrolidin-1-ylethoxy)phenyl]acetamide
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| 由来 | homo sapiens (ヒト)
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キーワード | TRANSFERASE/TRANSFERASE INHIBITOR / ALPHA AND BETA PROTEIN (A+B) / TRANSFERASE-TRANSFERASE INHIBITOR complex / TRANSFERASE |
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