タイトル Virtual screening and experimental validation reveal novel small-molecule inhibitors of 14-3-3 protein-protein interactions. ジャーナル・号・ページ Chem. Commun. (Camb. ) , Vol. 49, Page 8468-8470, Year 2013掲載日 2011年7月20日 (構造データの登録日) 著者Thiel, P. / Roglin, L. / Meissner, N. / Hennig, S. / Kohlbacher, O. / Ottmann, C. リンク Chem. Commun. (Camb. ) / PubMed:23939230手法 X線回折 解像度 1.4 - 1.8 Å 構造データ PDB-3t0l : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.6 Å
PDB-3t0m : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.62 Å
PDB-4dhm : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.7 Å
PDB-4dhn : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.8 Å
PDB-4dho : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.7 Å
PDB-4dhp : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.75 Å
PDB-4dhq : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.75 Å
PDB-4dhr : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.4 Å
PDB-4dhs : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.74 Å
PDB-4dht : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.8 Å
PDB-4dhu : 構造ビューア Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening手法 : X-RAY DIFFRACTION / 解像度 : 1.67 Å
化合物 ChemComp-1CT : 構造ビューア [2-(2-oxo-2-{[2-(trifluoromethyl)phenyl]amino}ethoxy)phenyl]phosphonic acid
ChemComp-2CT : 構造ビューア (2-{2-[(2,5-dimethoxyphenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
ChemComp-0KB : 構造ビューア [2-(2-oxo-2-{[3-(trifluoromethyl)phenyl]amino}ethoxy)phenyl]phosphonic acid
ChemComp-0KC : 構造ビューア {2-[2-(cyclopentylamino)-2-oxoethoxy]phenyl}phosphonic acid
ChemComp-Y09 : 構造ビューア (2-{2-[(3-methoxyphenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
ChemComp-Y07 : 構造ビューア [2-(2-{[2-chloro-5-(trifluoromethyl)phenyl]amino}-2-oxoethoxy)phenyl]phosphonic acid
ChemComp-Y06 : 構造ビューア (2-{2-[(3-chlorophenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
ChemComp-Y04 : 構造ビューア (2-{2-[(2-chlorophenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
ChemComp-Y03 : 構造ビューア (2-{2-[(3,5-dichlorophenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
ChemComp-0KG : 構造ビューア {2-[2-(cyclohexylamino)-2-oxoethoxy]phenyl}phosphonic acid
ChemComp-0KH : 構造ビューア (2-{2-[(2,3-dichlorophenyl)amino]-2-oxoethoxy}phenyl)phosphonic acid
由来 homo sapiens (ヒト) キーワード PROTEIN BINDING/INHIBITOR / Helical protein / Adapter protein / Protein-protein interaction / PROTEIN BINDING-INHIBITOR complex / PHOSPHOPROTEIN BINDING