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Crystal structure of hCA II in complex with Urea, N-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)-N'-(phenylmethyl)-

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Protein Data Bank Japan2024-01-24 更新2026-03-21 收录
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Crystal structure of hCA II in complex with Urea, N-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)-N'-(phenylmethyl)- Descriptor: 1-[7,7-bis(oxidanyl)-8-oxa-7-boranuidabicyclo[4.3.0]nona-1,3,5-trien-4-yl]-3-(phenylmethyl)urea, Carbonic anhydrase 2, ZINC ION Authors: Di Fiore, A, De Simone, G. Deposit date: 2019-05-31 Release date: 2019-08-28 Last modified: 2024-01-24 Method: X-RAY DIFFRACTION (1.58 Å) Cite: Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity. J Enzyme Inhib Med Chem, 34, 2019

与尿素衍生物N-(1,3-二氢-1-羟基-2,1-苯并氧杂硼杂环戊-6-基)-N'-(苯甲基)结合的人类碳酸酐酶2(hCA II,Carbonic anhydrase 2)晶体结构。描述符:1-[7,7-双(羟基)-8-氧杂-7-硼杂二环[4.3.0]壬-1,3,5-三烯-4-基]-3-(苯甲基)脲、碳酸酐酶2(Carbonic anhydrase 2)、锌离子(ZINC ION)。作者:Di Fiore, A、De Simone, G。提交日期:2019年5月31日;发布日期:2019年8月28日;最后修改日期:2024年1月24日。实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率1.58埃(Å)。引用文献:《探索苯并氧杂硼杂环戊衍生物作为碳酸酐酶抑制剂:结构与计算分析揭示其构象变异性可作为提升酶选择性的工具》,发表于《J Enzyme Inhib Med Chem》(全称:Journal of Enzyme Inhibition and Medicinal Chemistry),2019年,第34卷。
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2019-05-31
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