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K316A mutant of Enoyl-ACP Reductase from Plasmodium falciparum (PfENR) in complex with triclosan

NIAID Data Ecosystem2026-05-01 收录

抗疟药物靶点

抑制剂结构

数据链接：

https://www.rcsb.org/structure/3AM5 数据链接链接失效反馈

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资源简介：

K316A mutant of Enoyl-ACP Reductase from Plasmodium falciparum (PfENR) in complex with triclosan

应用场景：

创建时间：

2023-11-01

结核病药物靶点

抑制剂结构

Crystal structure of 3-dehydroquinate dehydratase from Mycobacterium tuberculosis in complex with inhibitor 4 Descriptor: (1R,5R)-1,5-dihydroxy-4-oxo-3-[3-oxo-3-(phenylamino)propyl]cyclohex-2-ene-1-ca

Protein Data Bank Japan2023-09-06 更新50

Manganese peroxidase complexed with Cd(II) inhibitor

抑制剂结构

重金属生物毒性研究

Manganese peroxidase complexed with Cd(II) inhibitor

NIAID Data Ecosystem30

Plasmodium vivax N-myristoyltransferase in complex with YnC12-CoA thioester.

疟原虫酶结构解析

抗疟药物靶点

Plasmodium vivax N-myristoyltransferase in complex with YnC12-CoA thioester. Descriptor: CHLORIDE ION, DIMETHYL SULFOXIDE, GLYCYLPEPTIDE N-TETRADECANOYLTRANSFERASE, ... Authors: Wright, M.H, Clough, B

Protein Data Bank Japan2024-05-08 更新20

Using in Vitro Evolution and Whole Genome Analysis To Discover Next Generation Targets for Antimalarial Drug Discovery

抗疟药物靶点

进化基因组学靶标验证

Although many new anti-infectives have been discovered and developed solely using phenotypic cellular screening and assay optimization, most researchers recognize that structure-guided drug design is

NIAID Data Ecosystem40

Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI26

抗病毒药物设计

抑制剂结构

Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI26 Descriptor: 3C-like proteinase, O-tert-butyl-N-{[(3-chlorophenyl)methoxy]carbonyl}-L-threonyl-N-{(2S)-1-hydroxy-3-[(3S)-2-oxop

Protein Data Bank Japan2024-10-30 更新30

K316A mutant of Enoyl-ACP Reductase from Plasmodium falciparum (PfENR) in complex with triclosan

资源简介：

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