The Crystal structure of mol066 bound to the main protease (3CLpro/Mpro) of SARS-CoV-2

NIAID Data Ecosystem2026-05-02 收录

蛋白质-配体共晶结构

抗新冠病毒药物设计

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The Crystal structure of mol066 bound to the main protease (3CLpro/Mpro) of SARS-CoV-2

创建时间：

2025-06-11

Cocrystal of BRD4(D1) with a selective inhibitor

蛋白质-配体共晶结构

BRD4抑制剂

Cocrystal of BRD4(D1) with a selective inhibitor Descriptor: 1,2-ETHANEDIOL, 4-(1-{1-[2-(dimethylamino)ethyl]piperidin-4-yl}-4-[4-(trifluoromethyl)phenyl]-1H-imidazol-5-yl)-N-(3,5-dimethylphenyl)pyrim

Protein Data Bank Japan2023-10-18 更新70

Targeting the PRC2 complex through a novel protein-protein interaction inhibitor of EED

PRC2复合物抑制剂

蛋白质-配体共晶结构

Targeting the PRC2 complex through a novel protein-protein interaction inhibitor of EED Descriptor: (3R,4S)-1-[(1S)-7-fluoro-2,3-dihydro-1H-inden-1-yl]-N,N-dimethyl-4-{4-[4-(methylsulfonyl)piperazin-1

Protein Data Bank Japan2023-09-27 更新60

Crystal structure of the human bromodomain of EP300 bound to the inhibitor XDM-CBP

蛋白质-配体共晶结构

表观遗传学药物设计

Crystal structure of the human bromodomain of EP300 bound to the inhibitor XDM-CBP Descriptor: 1,2-ETHANEDIOL, Histone acetyltransferase p300, ~{N}-[[2,8-bis(oxidanyl)naphthalen-1-yl]methyl]-4-ethanoy

Protein Data Bank Japan2024-01-17 更新40

Room-temperature X-ray structure of SARS-CoV-2 main protease catalytic domain (residues 1-199-6H) in complex with ensitrelvir (ESV)

蛋白-药物复合物结构解析

抗新冠病毒药物设计

Room-temperature X-ray structure of SARS-CoV-2 main protease catalytic domain (residues 1-199-6H) in complex with ensitrelvir (ESV)

NIAID Data Ecosystem60

Structure of the monofunctional Staphylococcus aureus PBP1 in its beta-lactam (Ertapenem) inhibited form

细菌耐药性机制

蛋白质-配体共晶结构

Structure of the monofunctional Staphylococcus aureus PBP1 in its beta-lactam (Ertapenem) inhibited form Descriptor: (4R,5S)-3-({(3S,5S)-5-[(3-carboxyphenyl)carbamoyl]pyrrolidin-3-yl}sulfanyl)-5-[(1S,

Protein Data Bank Japan2024-10-23 更新50

The Crystal structure of mol066 bound to the main protease (3CLpro/Mpro) of SARS-CoV-2

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