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	Structural studies of pterin-based inhibitors of dihydropteroate synthase.
ジャーナル・号・ページ	J. Med. Chem., Vol. 53, Page 166-177, Year 2010
掲載日	2009年4月14日 (構造データの登録日)
著者	Hevener, K.E. / Yun, M.K. / Qi, J. / Kerr, I.D. / Babaoglu, K. / Hurdle, J.G. / Balakrishna, K. / White, S.W. / Lee, R.E.
リンク	J. Med. Chem. / PubMed:19899766
手法	X線回折
解像度	2 - 2.7 Å
構造データ	PDB-3h21: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.32 Å PDB-3h22: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-3h23: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-3h24: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-3h26: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-3h2a: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-3h2c: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.6 Å PDB-3h2e: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.0 Å PDB-3h2f: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-3h2m: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.31 Å PDB-3h2n: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-3h2o: Structural Studies of Pterin-Based Inhibitors of Dihydropteroate Synthase 手法: X-RAY DIFFRACTION / 解像度: 2.7 Å
化合物	ChemComp-B52: (2R)-2-(7-amino-1-methyl-4,5-dioxo-1,4,5,6-tetrahydropyrimido[4,5-c]pyridazin-3-yl)propanoic acid ChemComp-SO4: SULFATE ION / 硫酸ジアニオン ChemComp-HOH: WATER ChemComp-B53: 2,6-diamino-5-nitrosopyrimidin-4(3H)-one / 2,4-ジアミノ-5-ニトロソピリミジン-6-オ-ル ChemComp-B54: 4-{3-[(2-amino-5-nitroso-6-oxo-1,6-dihydropyrimidin-4-yl)amino]propoxy}benzoic acid ChemComp-B55: 2-amino-8-sulfanyl-1,9-dihydro-6H-purin-6-one / 8-メルカプトグアニン ChemComp-B56: 2-amino-8-methyl-4-oxo-3,4,7,8-tetrahydropteridine-6-carboxylic acid ChemComp-B57: 2,6-diamino-5-nitropyrimidin-4(3H)-one ChemComp-B58: 1H-imidazo[4,5-d]pyridazine-4,7-diamine / 4,7-ジアミノ-1H-イミダゾ[4,5-d]ピリダジン ChemComp-B59: 1,3-dimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydropteridine-6-carbaldehyde ChemComp-B60: 2-amino-8-methyl-7,8-dihydropteridin-4(3H)-one ChemComp-B61: 2-amino-6-(2-hydroxy-2-methylpropyl)-8-methyl-7,8-dihydropteridin-4(3H)-one ChemComp-B62: (6R)-2-amino-6-methyl-5,6,7,8-tetrahydropteridin-4(3H)-one / 2-アミノ-6α-メチル-5,6,7,8-テトラヒドロプテリジン-4(1H)-オン ChemComp-B63: 4-{[2-(2-amino-4-oxo-3,4,7,8-tetrahydropteridin-6-yl)ethyl]amino}benzoic acid
由来	bacillus anthracis str. a2012 (炭疽菌)
キーワード	Transferase/Transferase Inhibitor / ANTHRACIS / FOLATE BIOSYNTHESIS / DIHYDROPTEROATE / PTERINE / Transferase / Transferase-Transferase Inhibitor COMPLEX