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Threonyl-tRNA synthetase from Salmonella enterica in complex with an inhibitor

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Protein Data Bank Japan2023-11-29 更新2026-04-19 收录
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Threonyl-tRNA synthetase from Salmonella enterica in complex with an inhibitor Descriptor: (2S,3R)-2-azanyl-N-[(1R)-2-[3-(7-bromanyl-6-chloranyl-4-oxidanylidene-quinazolin-3-yl)propanoylamino]-1-(3-phenylphenyl)ethyl]-3-oxidanyl-butanamide, 1,2-ETHANEDIOL, Threonine--tRNA ligase, ... Authors: Cai, Z, Chen, B, Yu, Y, Zhou, H. Deposit date: 2022-01-14 Release date: 2022-04-27 Last modified: 2023-11-29 Method: X-RAY DIFFRACTION (2 Å) Cite: Design, Synthesis, and Proof-of-Concept of Triple-Site Inhibitors against Aminoacyl-tRNA Synthetases. J.Med.Chem., 65, 2022

本数据集为肠炎沙门氏菌(Salmonella enterica)来源的苏氨酰-tRNA合成酶(Threonyl-tRNA synthetase,亦称为苏氨酸-tRNA连接酶Threonine--tRNA ligase)与抑制剂结合的复合物体系。复合物组分包括抑制剂(2S,3R)-2-氨基-N-[(1R)-2-[3-(7-溴-6-氯-4-氧代喹唑啉-3-基)丙酰氨基]-1-(3-苯基苯基)乙基]-3-羟基丁酰胺、1,2-乙二醇(1,2-ETHANEDIOL)及其他未列明组分。作者:蔡Z、陈B、余Y、周H。提交日期:2022-01-14;发布日期:2022-04-27;最后修改日期:2023-11-29。实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率为2埃(2 Å)。引用文献:《抗氨酰-tRNA合成酶三位点抑制剂的设计、合成与概念验证》(Design, Synthesis, and Proof-of-Concept of Triple-Site Inhibitors against Aminoacyl-tRNA Synthetases),刊载于《药物化学杂志》(J.Med.Chem.),2022年,第65卷。
创建时间:
2022-01-14
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