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Dna gyrase atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor (4-[(1S,5R,6R)-6-AMINO-1-METHYL-3-AZABICYCLO[3.2.0]HEPT-3-YL]-6-FLUORO-N-METHYL-2-[(2-METHYLPYRIMIDIN-5-YL)OXY]-9H-PYRIMIDO[4,5-B]INDOL-8-AMINE)

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Protein Data Bank Japan2024-02-28 更新2026-03-21 收录
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https://pdbj.org/mine/summary/4ksg
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Dna gyrase atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor (4-[(1S,5R,6R)-6-AMINO-1-METHYL-3-AZABICYCLO[3.2.0]HEPT-3-YL]-6-FLUORO-N-METHYL-2-[(2-METHYLPYRIMIDIN-5-YL)OXY]-9H-PYRIMIDO[4,5-B]INDOL-8-AMINE) Descriptor: 4-[(1S,5R,6R)-6-amino-1-methyl-3-azabicyclo[3.2.0]hept-3-yl]-6-fluoro-N-methyl-2-[(2-methylpyrimidin-5-yl)oxy]-9H-pyrimido[4,5-b]indol-8-amine, DNA gyrase subunit B, TERTIARY-BUTYL ALCOHOL Authors: Bensen, D.C, Akers-Rodriguez, S, Tari, L.W. Deposit date: 2013-05-17 Release date: 2014-01-15 Last modified: 2024-02-28 Method: X-RAY DIFFRACTION (1.75 Å) Cite: A new class of type iia topoisomerase inhibitors with broad-spectrum antibacterial activity To be Published

粪肠球菌(Enterococcus faecalis)DNA旋转酶(DNA gyrase)ATP结合结构域与小分子抑制剂4-[(1S,5R,6R)-6-氨基-1-甲基-3-氮杂双环[3.2.0]庚-3-基]-6-氟-N-甲基-2-[(2-甲基嘧啶-5-基)氧基]-9H-嘧啶并[4,5-b]吲哚-8-胺形成的复合物;描述项:4-[(1S,5R,6R)-6-氨基-1-甲基-3-氮杂双环[3.2.0]庚-3-基]-6-氟-N-甲基-2-[(2-甲基嘧啶-5-基)氧基]-9H-嘧啶并[4,5-b]吲哚-8-胺、DNA旋转酶B亚基、叔丁醇(TERTIARY-BUTYL ALCOHOL);作者:本森(Bensen, D.C.)、阿克斯-罗德里格斯(Akers-Rodriguez, S)、塔里(Tari, L.W.);存放日期:2013年5月17日;发布日期:2014年1月15日;最后修改日期:2024年2月28日;实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率1.75埃(Å);引用文献:一类具备广谱抗菌活性的IIA型拓扑异构酶抑制剂新类别(待发表)
创建时间:
2013-05-17
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