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资源简介:
SARS-CoV2 and Drug-target shortest distance
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创建时间:
2020-11-01
相关数据集
Fab RVFV-268
Fab RVFV-268 Descriptor: CITRIC ACID, Heavy chain Fab268, Light chain Fab268 Authors: Hulswit, R.J.G, Bowden, T.A, Stass, R. Deposit date: 2022-08-30 Release date: 2023-09-06 Last modified: 2026-03-04
Protein Data Bank Japan2026-03-04 更新50
Group deposition for crystallographic fragment screening of Coxsackievirus A16 (G-10) 2A protease -- Crystal structure of Coxsackievirus A16 (G-10) 2A protease in complex with Z57473948 (A71EV2A-x1292)
Group deposition for crystallographic fragment screening of Coxsackievirus A16 (G-10) 2A protease -- Crystal structure of Coxsackievirus A16 (G-10) 2A protease in complex with Z57473948 (A71EV2A-x1292
Protein Data Bank Japan2024-10-16 更新20
Data for Figs 1, S2 and S3.
Human cytomegalovirus (HCMV) is an important pathogen for which new antiviral drugs are needed. HCMV, like other herpesviruses, encodes a nuclear egress complex (NEC) composed of two subunits, UL50 an
NIAID Data Ecosystem10
Table1_Identification of compelling inhibitors of human norovirus 3CL protease to combat gastroenteritis: A structure-based virtual screening and molecular dynamics study.docx
Human noroviruses (NV) are the most prevalent cause of sporadic and pandemic acute gastroenteritis. NV infections cause substantial morbidity and death globally, especially amongst the aged, immunocom
NIAID Data Ecosystem30
Additional file 1 of Identifying FDA-approved drugs with multimodal properties against COVID-19 using a data-driven approach and a lung organoid model of SARS-CoV-2 entry
Additional file 1: Table S1. Genes differentially expressed in lung cancer cells after exposure to SARS-CoV-2. Source: Blanco-Melo et al. (2020). Table S2. Connectivity mapping results generated by qu
Figshare2021-10-05 更新10



