タイトル | Structure-guided discovery of cyclin-dependent kinase inhibitors. |
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ジャーナル・号・ページ | Biopolymers, Vol. 89, Page 372-379, Year 2008 |
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掲載日 | 2007年8月29日 (構造データの登録日) |
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著者 | Fischmann, T.O. / Hruza, A. / Duca, J.S. / Ramanathan, L. / Mayhood, T. / Windsor, W.T. / Le, H.V. / Guzi, T.J. / Dwyer, M.P. / Paruch, K. ...Fischmann, T.O. / Hruza, A. / Duca, J.S. / Ramanathan, L. / Mayhood, T. / Windsor, W.T. / Le, H.V. / Guzi, T.J. / Dwyer, M.P. / Paruch, K. / Doll, R.J. / Lees, E. / Parry, D. / Seghezzi, W. / Madison, V. |
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リンク | Biopolymers / PubMed:17937404 |
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手法 | X線回折 |
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解像度 | 1.28 - 1.8 Å |
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構造データ | PDB-2r3f: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.5 Å PDB-2r3g: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.55 Å PDB-2r3h: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.5 Å PDB-2r3i: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.28 Å PDB-2r3j: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.65 Å PDB-2r3k: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.7 Å PDB-2r3l: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.65 Å PDB-2r3m: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.7 Å PDB-2r3n: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.63 Å PDB-2r3o: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å PDB-2r3p: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.66 Å PDB-2r3q: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.35 Å PDB-2r3r: Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.47 Å |
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化合物 | ChemComp-5SC: 3-((3-bromo-5-o-tolylpyrazolo[1,5-a]pyrimidin-7-ylamino)methyl)pyridine 1-oxide
ChemComp-6SC: 3-bromo-5-phenyl-N-(pyridin-4-ylmethyl)pyrazolo[1,5-a]pyrimidin-7-amine
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由来 | - homo sapiens (ヒト)
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キーワード | TRANSFERASE / SERINE/THREONINE-PROTEIN KINASE / CELL CYCLE / INHIBITION / CYCLIN-DEPENDENT KINASE / CANCER / ATP-binding / Cell division / Mitosis / Nucleotide-binding / Phosphorylation / Polymorphism |
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