EMDB/PDB/SASBDBから引用されている文献のデータベース

キーワード
構造解析手法	All X線回折 NMR 電子顕微鏡小角散乱中性子線回折線維回折粉末回折赤外分光 EPR FRET 理論モデルハイブリッド
著者・登録者
ジャーナル
IF	>30 >20 >10 >5 all

タイトル	Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding
ジャーナル・号・ページ	TO BE PUBLISHED
掲載日	2010年4月26日 (構造データの登録日)
著者	Namboodiri, H.V. / Springman, E.B. / Karpusas, M. / Bukhtiyarova, M. / Ramcharan, J.
リンク	PubMedで検索
手法	X線回折
解像度	2 - 2.8 Å
構造データ	PDB-3mpa: Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-3o8p: Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-3o8t: Conformational plasticity of p38 MAP kinase DFG-motif mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2 Å PDB-3o8u: Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-3obg: Conformational plasticity of p38 MAP kinase DFG mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.8 Å PDB-3obj: Conformational plasticity of p38 MAP kinase DFG mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-3oc1: Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding 手法: X-RAY DIFFRACTION / 解像度: 2.59 Å
化合物	ChemComp-SB2: 4-[5-(4-FLUORO-PHENYL)-2-(4-METHANESULFINYL-PHENYL)-3H-IMIDAZOL-4-YL]-PYRIDINE ChemComp-BOG: octyl beta-D-glucopyranoside / 可溶化剤YM ChemComp-HOH: WATER ChemComp-BMU: 1-(5-TERT-BUTYL-2-METHYL-2H-PYRAZOL-3-YL)-3-(4-CHLORO-PHENYL)-UREA ChemComp-EDO*: 1,2-ETHANEDIOL
由来	homo sapiens (ヒト)
キーワード	TRANSFERASE