CARM1 in complex with EML982
收藏Protein Data Bank Japan2024-01-31 更新2026-05-23 收录
下载链接:
https://pdbj.org/mine/summary/7puq
下载链接
链接失效反馈官方服务:
资源简介:
CARM1 in complex with EML982 Descriptor: 1,2-ETHANEDIOL, Histone-arginine methyltransferase CARM1, methyl 6-[4-[[~{N}-[3-[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]propyl]carbamimidoyl]amino]butylcarbamoylamino]-4-oxidanyl-naphthalene-2-carboxylate Authors: Marechal, N, Cura, V, Troffer-Charlier, N, Bonnefond, L, Cavarelli, J. Deposit date: 2021-09-30 Release date: 2022-04-06 Last modified: 2024-01-31 Method: X-RAY DIFFRACTION (2.09 Å) Cite: Turning Nonselective Inhibitors of Type I Protein Arginine Methyltransferases into Potent and Selective Inhibitors of Protein Arginine Methyltransferase 4 through a Deconstruction-Reconstruction and Fragment-Growing Approach. J.Med.Chem., 65, 2022
与EML982结合的CARM1
数据集描述项:1,2-乙二醇、组蛋白精氨酸甲基转移酶CARM1、6-[4-[[N-[3-[(2R,3S,4R,5R)-5-(6-氨基嘌呤-9-基)-3,4-二羟基四氢呋喃-2-基]丙基]脒基]氨基]丁基氨基甲酰氨基]-4-羟基-2-萘甲酸甲酯
作者:Marechal N、Cura V、Troffer-Charlier N、Bonnefond L、Cavarelli J
存储日期:2021-09-30
发布日期:2022-04-06
最后修改日期:2024-01-31
实验方法:X射线衍射(分辨率2.09埃)
引用文献:通过解构-重建与片段生长策略将I型蛋白精氨酸甲基转移酶的非选择性抑制剂转化为蛋白精氨酸甲基转移酶4的强效选择性抑制剂,《药物化学杂志》,2022年,第65卷
创建时间:
2021-09-30



