Crystal Structure of the Prototype Foamy Virus Intasome with a 2-Pyridinone Aminal Inhibitor

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Crystal Structure of the Prototype Foamy Virus Intasome with a 2-Pyridinone Aminal Inhibitor

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2024-03-06

Structure of FIPV main protease in complex with dual inhibitors

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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

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Molecular docking: Hydroxychloroquine alternative to inhibit the COVID-19 main protease (MPro)

计算药物筛选

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Docking study shows best binding affinity against the main protease of COVID-19. Email ID: contact@findrug.org

Figshare2020-05-09 更新60

Crystal structure of HCV NS3/4A D168A protease in complex with NR02-49

丙肝病毒蛋白结构

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Crystal structure of HCV NS3/4A D168A protease in complex with NR02-49 Descriptor: 1,2-ETHANEDIOL, NS3/4A protease, SULFATE ION, ... Authors: Zephyr, J, Schiffer, C.A. Deposit date: 2021-04-29 Release

Protein Data Bank Japan2023-10-18 更新50

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 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

Crystal Structure of the Prototype Foamy Virus Intasome with a 2-Pyridinone Aminal Inhibitor

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