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CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS INTASOME WITH A 2- PYRIDINONE AMINAL INHIBITOR (COMPOUND 31)

NIAID Data Ecosystem2026-05-01 收录

病毒整合酶

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CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS INTASOME WITH A 2- PYRIDINONE AMINAL INHIBITOR (COMPOUND 31)

应用场景：

创建时间：

2024-03-06

抗病毒药物设计

结构生物学

Structure of FIPV main protease in complex with dual inhibitors Descriptor: 1,2-ETHANEDIOL, N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-N~1~-((1R,2Z)-4-(BENZYLOXY)-4-OXO-1-{[(3R)-2-OXOPYRROLIDIN

Protein Data Bank Japan2024-11-13 更新100

Crystal structure of HCV NS3/4A D168A protease in complex with PC (JZ01-15)

丙肝病毒蛋白结构

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Crystal structure of HCV NS3/4A D168A protease in complex with PC (JZ01-15) Descriptor: 1,2-ETHANEDIOL, GLYCEROL, NS3 protease, ... Authors: Zephyr, J, Schiffer, C.A. Deposit date: 2019-09-20 Release

Protein Data Bank Japan2023-10-11 更新70

Crystal Structure of uncleaved SARS-CoV-2 Main Protease C145S mutant in complex with Nirmatrelvir

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蛋白质晶体学

Crystal Structure of uncleaved SARS-CoV-2 Main Protease C145S mutant in complex with Nirmatrelvir Descriptor: (1R,2S,5S)-N-{(1E,2S)-1-imino-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-6,6-dimethyl-3-[3-

Protein Data Bank Japan2024-10-16 更新50

Crystallization and structure determination of the core-binding domain of bacteriophage lambda integrase

蛋白质晶体学

病毒整合酶

Crystallization and structure determination of the core-binding domain of bacteriophage lambda integrase Descriptor: Integrase, SULFATE ION Authors: Kamadurai, H.B, Jain, R, Foster, M.P. Deposit date:

Protein Data Bank Japan2024-02-21 更新80

Structure-Based Stabilization of Non-native Protein–Protein Interactions of Coronavirus Nucleocapsid Proteins in Antiviral Drug Design

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蛋白质相互作用

Structure-based stabilization of protein–protein interactions (PPIs) is a promising strategy for drug discovery. However, this approach has mainly focused on the stabilization of native PPIs, and non-

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CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS INTASOME WITH A 2- PYRIDINONE AMINAL INHIBITOR (COMPOUND 31)

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