Author

Katerina Artavanis‐Tsakonas

University of CambridgeORCID 0000-0003-1164-1965Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:plant (other)· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:proteomics· 1

Frequent Co-Authors

Adán Pinto-FernándeziD· 1 shared Alexander A. VinogradoviD· 1 shared Benedikt Mathias KessleriD· 1 shared Cameron L. C. SmithiD· 1 shared David Benjamin AscheriD· 1 shared Geoff P. KellyiD· 1 shared Gerbrand J. van der Heden van NoortiD· 1 shared Harry R. King· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

Adán Pinto-FernándezORCID

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2 papers

Recent·Most cited

Cell BiologyPLoS PathogensPeer-reviewedApr 18, 2025

Identification of a new Plasmodium falciparum E2 ubiquitin conjugating enzyme

Cameron L. C. Smith, Mohsen Hajisadeghian, Gerbrand J. van der Heden van Noort…·Katerina Artavanis‐Tsakonas

The paper identifies a new E2 ubiquitin-conjugating enzyme in Plasmodium falciparum using a ubiquitin-activity based probe and validates its function through structural and biochemical analysis.

2 citations

plant (other)experimental assay

𝕏 PostBluesky

BiophysicsProceedings of the National Academy of SciencesPeer-reviewedMay 13, 2024

Targeting the Plasmodium falciparum UCHL3 ubiquitin hydrolase using chemically constrained peptides

Harry R. King, Mark Bycroft, Thanh Nguyen…·Katerina Artavanis‐Tsakonas

This study identifies chemically constrained peptides that inhibit PfUCHL3, a critical deubiquitinating enzyme in Plasmodium falciparum, by blocking substrate binding rather than active site interaction.

4 citations

plant (other)proteomics

𝕏 PostBluesky