FTase in complex with BMS analogue 13
收藏Protein Data Bank Japan2023-11-08 更新2026-03-21 收录
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FTase in complex with BMS analogue 13 Descriptor: 4-({(3R)-7-cyano-4-[(4-methoxyphenyl)sulfonyl]-1-[(1-methyl-1H-imidazol-5-yl)methyl]-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-yl}methyl)phenyl diethylcarbamate, DIMETHYL SULFOXIDE, FARNESYL DIPHOSPHATE, ... Authors: Guo, Z, Stigter, E.A, Bon, R.S, Waldmann, H, Blankenfeldt, W, Goody, R.S. Deposit date: 2012-08-29 Release date: 2012-10-24 Last modified: 2023-11-08 Method: X-RAY DIFFRACTION (2.2 Å) Cite: Development of Selective, Potent RabGGTase Inhibitors J.Med.Chem., 55, 2012
法尼基转移酶(FTase,Farnesyltransferase)与BMS类似物13形成的复合物。组分描述:4-({(3R)-7-氰基-4-[(4-甲氧基苯基)磺酰基]-1-[(1-甲基-1H-咪唑-5-基)甲基]-2,3,4,5-四氢-1H-1,4-苯并二氮杂䓬-3-基}甲基)苯基二乙基氨基甲酸酯、二甲基亚砜(DIMETHYL SULFOXIDE)、法尼基二磷酸(FARNESYL DIPHOSPHATE)等。作者:Guo, Z、Stigter, E.A、Bon, R.S、Waldmann, H、Blankenfeldt, W、Goody, R.S。收录日期:2012-08-29;发布日期:2012-10-24;最后修改日期:2023-11-08。实验方法:X射线衍射(分辨率2.2埃)。引用文献:《选择性强效Rab香叶基香叶酰转移酶(RabGGTase)抑制剂的开发》,《Journal of Medicinal Chemistry》(J.Med.Chem.),第55卷,2012年。
创建时间:
2012-08-29



