タイトル | Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site. |
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ジャーナル・号・ページ | Acta Crystallogr D Struct Biol, Vol. 72, Page 682-693, Year 2016 |
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掲載日 | 2015年5月13日 (構造データの登録日) |
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著者 | Chen, H. / Tucker, J. / Wang, X. / Gavine, P.R. / Phillips, C. / Augustin, M.A. / Schreiner, P. / Steinbacher, S. / Preston, M. / Ogg, D. |
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リンク | Acta Crystallogr D Struct Biol / PubMed:27139631 |
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手法 | X線回折 |
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解像度 | 1.65 - 2.79 Å |
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構造データ | PDB-4zsg: MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR 手法: X-RAY DIFFRACTION / 解像度: 1.79 Å PDB-4zsj: MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR 手法: X-RAY DIFFRACTION / 解像度: 2.48 Å PDB-4zsl: MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR 手法: X-RAY DIFFRACTION / 解像度: 2.25 Å PDB-5byy: ERK5 IN COMPLEX WITH SMALL MOLECULE 手法: X-RAY DIFFRACTION / 解像度: 2.79 Å PDB-5byz: ERK5 in complex with small molecule 手法: X-RAY DIFFRACTION / 解像度: 1.65 Å |
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化合物 | ChemComp-4QX: 3-amino-5-[(4-chlorophenyl)amino]-N-(propan-2-yl)-1H-1,2,4-triazole-1-carboxamide
ChemComp-4R0: 3-amino-5-[(4-chloro-3-methylphenyl)amino]-N-(propan-2-yl)-1H-1,2,4-triazole-1-carboxamide
ChemComp-4QZ: 3-amino-5-[(4-chlorophenyl)amino]-N-[(1S)-1-phenylethyl]-1H-1,2,4-triazole-1-carboxamide
ChemComp-4WG: 2-{[2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl]amino}-5,11-dimethyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one
ChemComp-4WE: 4-({5-fluoro-4-[2-methyl-1-(propan-2-yl)-1H-imidazol-5-yl]pyrimidin-2-yl}amino)-N-[2-(piperidin-1-yl)ethyl]benzamide
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由来 | - homo sapiens (ヒト)
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キーワード | KINASE / INHIBITOR / TRANSFERASE / ERK5 KINASE / kinase inhibitor / PROTEROS BIOSTRUCTURES GMBH / ERk5 |
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