Crystal Structure of BoNT/A LC complexed with Hydroxamate-based Inhibitor PT-3

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蛋白酶-抑制剂复合物结构

神经毒素抑制剂

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Crystal Structure of BoNT/A LC complexed with Hydroxamate-based Inhibitor PT-3

创建时间：

2023-09-13

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

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

Crystal structure of acetylpolyamine amidohydrolase from Mycoplana ramosa in complex with a trifluoromethylketone inhibitor

蛋白酶-抑制剂复合物结构

药物设计

Crystal structure of acetylpolyamine amidohydrolase from Mycoplana ramosa in complex with a trifluoromethylketone inhibitor

NIAID Data Ecosystem30

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

Crystal Structure of BoNT/A LC complexed with Hydroxamate-based Inhibitor PT-3

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