| タイトル | Structural basis of inhibitor selectivity in MAP kinases. |
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| ジャーナル・号・ページ | Structure, Vol. 6, Page 1117-1128, Year 1998 |
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| 掲載日 | 1998年4月10日 (構造データの登録日) |
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著者 | Wang, Z. / Canagarajah, B.J. / Boehm, J.C. / Kassisa, S. / Cobb, M.H. / Young, P.R. / Abdel-Meguid, S. / Adams, J.L. / Goldsmith, E.J. |
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リンク | Structure / PubMed:9753691 |
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| 手法 | X線回折 |
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| 解像度 | 2.1 - 2.5 Å |
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| 構造データ | PDB-1a9u: THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB203580 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-1bl6: THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB216995 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-1bl7: THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB220025 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-1bmk: THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB218655 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-3erk: THE COMPLEX STRUCTURE OF THE MAP KINASE ERK2/SB220025 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-4erk: THE COMPLEX STRUCTURE OF THE MAP KINASE ERK2/OLOMOUCINE 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å |
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| 化合物 | ChemComp-SB2: 4-[5-(4-FLUORO-PHENYL)-2-(4-METHANESULFINYL-PHENYL)-3H-IMIDAZOL-4-YL]-PYRIDINE
ChemComp-SB6: 4-(4-FLUOROPHENYL)-1-CYCLOROPROPYLMETHYL-5-(4-PYRIDYL)-IMIDAZOLE
ChemComp-SB4: 4-(4-FLUOROPHENYL)-1-(4-PIPERIDINYL)-5-(2-AMINO-4-PYRIMIDINYL)-IMIDAZOLE
ChemComp-SB5: 4-(FLUOROPHENYL)-1-CYCLOPROPYLMETHYL-5-(2-AMINO-4-PYRIMIDINYL)IMIDAZOLE
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| 由来 | homo sapiens (ヒト) rattus norvegicus (ドブネズミ)
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キーワード | TRANSFERASE / MAP KINASE / SERINE/THREONINE-PROTEIN KINASE / P38 / INHIBITORS / SERINE/ THREONINE-PROTEIN KINASE / INHIBITOR / ERK2 |
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