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PSEUDOMONAS SERINE-CARBOXYL PROTEINASE (SEDOLISIN) COMPLEXED WITH THE INHIBITOR AIPF

NIAID Data Ecosystem2026-05-01 收录

蛋白酶-抑制剂复合物结构

结构生物学与药物设计

数据链接：

https://www.rcsb.org/structure/6M8Y 数据链接链接失效反馈

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资源简介：

PSEUDOMONAS SERINE-CARBOXYL PROTEINASE (SEDOLISIN) COMPLEXED WITH THE INHIBITOR AIPF

应用场景：

创建时间：

2023-10-11

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

Structure of Bacillus subtilis Nitric Oxide Synthase in complex with 3,5-bis(2-(6-amino-4-methylpyridin-2-yl)ethyl)benzonitrile

蛋白酶-抑制剂复合物结构

药物靶点识别

Structure of Bacillus subtilis Nitric Oxide Synthase in complex with 3,5-bis(2-(6-amino-4-methylpyridin-2-yl)ethyl)benzonitrile Descriptor: 3,5-bis[2-(6-amino-4-methylpyridin-2-yl)ethyl]benzonitrile,

Protein Data Bank Japan2023-12-20 更新40

Development of novel small molecules to target cellular pathways

药物靶向发现

结构生物学与药物设计

Small molecules represent powerful tools to dissect physiological and pathological states of signaling pathways, yet require characterization through X-ray crystallography. This...

B2FIND30

Solution structure of HPPK in complex with inhibitor analog AMPCPP

蛋白酶-抑制剂复合物结构

生物合成途径

Solution structure of HPPK in complex with inhibitor analog AMPCPP

NIAID Data Ecosystem40

Mycobacterium tuberculosis DprE1 in complex with CT325 - hexagonal crystal form

结核分枝杆菌药物靶点

蛋白酶-抑制剂复合物结构

Mycobacterium tuberculosis DprE1 in complex with CT325 - hexagonal crystal form Descriptor: 3-(hydroxyamino)-N-[(1R)-1-phenylethyl]-5-(trifluoromethyl)benzamide, FLAVIN-ADENINE DINUCLEOTIDE, oxidoredu

Protein Data Bank Japan2024-11-20 更新40

PSEUDOMONAS SERINE-CARBOXYL PROTEINASE (SEDOLISIN) COMPLEXED WITH THE INHIBITOR AIPF

资源简介：

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