Author

F. H. M. Koua

Primary ORCID profile (0000-0001-8371-9587 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

F. H. M. KouaiD1 paper · European X-Ray Free-Electron Laser

Biology Disciplines

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Biochemistry· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:Drosophila· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:protein folding & dynamics· 1 Assay:protein structure· 1 Assay:structural biology· 1 Organism:virus· 1

Frequent Co-Authors

H. Han· 2 shared L. Brings· 2 shared A. Luana C Barra· 1 shared A. P. Mancuso· 1 shared B. Alves Franca· 1 shared C. Schmidt· 1 shared D. Bruna Leal Oliveira· 1 shared D. Turk· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersBiochemistry

H. Han

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2 papers

Recent·Most cited

Heterologous expression, purification and structural features of native Dictyostelium discoideum dye-decolorizing peroxidase bound to a natively incorporated heme

O. Kalkan, S. Kantamneni, L. Brings, H. Han, A. P. Mancuso, F. H. M. Koua

This study expresses and purifies a functional DdDyP peroxidase with native heme incorporation, determines its structure, and reveals key catalytic site features.

bioRxiv · May 8, 2023 · PreprintBiochemistry

SARS-CoV-2 papain-like protease PLpro in complex with natural compounds reveal allosteric sites for antiviral drug design

V. Srinivasan, H. Brognaro, P. R. Prabhu, E. E. de Souza, S. Guenther, P. Y. A. Reinke, T. J. Lane, H. Ginn, H. Han, W. Ewert, J. Sprenger, F. H. M. Koua, S. Falke, N. Werner, H. Andaleeb, , P

This study identifies three natural compounds that inhibit SARS-CoV-2 PLpro by binding to the ISG15/Ub-S2 allosteric site, showing antiviral activity and potential for drug design.

Communications Biology · Aug 11, 2022Peer-reviewedBiochemistry