Structure of GluK1 ligand-binding domain (S1S2) in complex with (2S,4R)-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid at 3.18 A resolution
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Structure of GluK1 ligand-binding domain (S1S2) in complex with (2S,4R)-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid at 3.18 A resolution Descriptor: (2~{S},4~{R})-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid, CHLORIDE ION, Glutamate receptor ionotropic, ... Authors: Frydenvang, K, Kastrup, J.S, Kristensen, C.M. Deposit date: 2016-10-13 Release date: 2017-01-11 Last modified: 2024-10-23 Method: X-RAY DIFFRACTION (3.18 Å) Cite: Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic Acid. J. Med. Chem., 60, 2017
分辨率为3.18埃的GluK1配体结合结构域(S1S2)与(2S,4R)-4-(2-羧基苯氧基)吡咯烷-2-羧酸的复合物结构
描述项:(2S,4R)-4-(2-羧基苯氧基)吡咯烷-2-羧酸、氯离子、离子型谷氨酸受体……
作者:Frydenvang K、Kastrup J.S.、Kristensen C.M.
提交日期:2016-10-13
发布日期:2017-01-11
最后修改日期:2024-10-23
实验方法:X射线衍射(3.18 Å)
引用文献:《一系列L-反式-4-取代脯氨酸的设计与合成:作为离子型谷氨酸受体的选择性拮抗剂——含新型亚型选择性红藻氨酸受体1型(GluK1)拮抗剂(2S,4R)-4-(2-羧基苯氧基)吡咯烷-2-羧酸的功能与X射线晶体学研究》,《药物化学杂志》(J. Med. Chem.),第60卷,2017年
创建时间:
2016-10-13



