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6VBR

The crystal structure of the 2009 H1N1/California PA endonuclease wild type in complex with SJ000986248

Summary for 6VBR
Entry DOI10.2210/pdb6vbr/pdb
Related5vpt
DescriptorPolymerase acidic protein, MANGANESE (II) ION, Hexa Vinylpyrrolidone K15, ... (6 entities in total)
Functional Keywordsnuclease, influenza, inhibitor resistance, hydrolase, viral protein, viral protein-inhibitor complex, viral protein/inhibitor
Biological sourceInfluenza A virus (A/Luxembourg/43/2009(H1N1))
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Total number of polymer chains1
Total formula weight24530.65
Authors
Cuypers, M.G.,Slavish, P.J.,Rankovic, Z.,White, S.W. (deposition date: 2019-12-19, release date: 2021-02-10, Last modification date: 2023-10-25)
Primary citationSlavish, P.J.,Cuypers, M.G.,Rimmer, M.A.,Abdolvahabi, A.,Jeevan, T.,Kumar, G.,Jarusiewicz, J.A.,Vaithiyalingam, S.,Jones, J.C.,Bowling, J.J.,Price, J.E.,DuBois, R.M.,Min, J.,Webby, R.J.,Rankovic, Z.,White, S.W.
Chemical scaffold recycling: Structure-guided conversion of an HIV integrase inhibitor into a potent influenza virus RNA-dependent RNA polymerase inhibitor designed to minimize resistance potential.
Eur.J.Med.Chem., 247:115035-115035, 2023
Cited by
PubMed: 36603507
DOI: 10.1016/j.ejmech.2022.115035
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.75 Å)
Structure validation

220472

数据于2024-05-29公开中

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