Mycobacterial adenylyl cyclase Rv1264, holoenzyme, inhibited state

NIAID Data Ecosystem2026-05-01 收录

结核病药物靶点

酶抑制机制

数据链接：

https://www.rcsb.org/structure/1Y10 数据链接链接失效反馈

官方服务：

资源简介：

Mycobacterial adenylyl cyclase Rv1264, holoenzyme, inhibited state

创建时间：

2024-04-03

Structure of the C13.18 RNA Aptamer in Complex with G Protein-Coupled Receptor Kinase 2

RNA适体

酶抑制机制

Structure of the C13.18 RNA Aptamer in Complex with G Protein-Coupled Receptor Kinase 2 Descriptor: Beta-adrenergic receptor kinase 1, C13.18 RNA Aptamer, MAGNESIUM ION Authors: Tesmer, J.J.G, Tesmer,

Protein Data Bank Japan2023-09-13 更新110

The Structure of F1-ATPase inhibited by quercetin.

酶抑制机制

ATP合成酶结构

The Structure of F1-ATPase inhibited by quercetin. Descriptor: 3,5,7,3',4'-PENTAHYDROXYFLAVONE, ADENOSINE-5'-DIPHOSPHATE, ATP SYNTHASE GAMMA CHAIN, ... Authors: Gledhill, J.R, Montgomery, M.G, Leslie,

Protein Data Bank Japan2023-12-13 更新50

M. tuberculosis DprE1 covalently bound to a nitrobenzoxacinone.

结核病药物靶点

蛋白酶-抑制剂复合物结构

M. tuberculosis DprE1 covalently bound to a nitrobenzoxacinone. Descriptor: 2-[(2~{S},6~{R})-2,6-dimethylpiperidin-1-yl]-8-nitro-6-(trifluoromethyl)-1,3-benzoxazin-4-one, Decaprenylphosphoryl-beta-D-r

Protein Data Bank Japan2024-11-13 更新40

Crystal structure of dihydrofolate reductase from Mycobacterium ulcerans with SDDC-0001565 inhibitor

结核病药物靶点

蛋白质晶体

Crystal structure of dihydrofolate reductase from Mycobacterium ulcerans with SDDC-0001565 inhibitor Descriptor: 1,2-ETHANEDIOL, 3-(3-{3-[(2,4-diamino-6-ethylpyrimidin-5-yl)oxy]propoxy}phenyl)propanoi

Protein Data Bank Japan2023-10-11 更新50

M. tb EgtD in complex with HD2

结核病药物靶点

蛋白质-配体复合物结构

M. tb EgtD in complex with HD2

NIAID Data Ecosystem50