Author

Johanna Kliche

Uppsala UniversityORCID 0000-0003-3179-4635Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Johanna Kliche1 paper · Department of Chemistry for Life Sciences, Uppsala University, Husargatan 3, 751 23 Uppsala, Sweden;

Biology Disciplines

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Biochemistry· 1 Cell Biology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 1

Frequent Co-Authors

Norman E. DaveyiD· 3 shared Caroline BenziD· 2 shared Matthew J. Winters· 2 shared Mythili S. Subbanna· 2 shared Peter M. PryciakiD· 2 shared Ylva IvarssoniD· 2 shared Aimiliani KonstantinouiD· 1 shared Amelie SteiniD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersBiochemistry

Norman E. DaveyORCID

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3 papers

Recent·Most cited

An Atlas of Short Linear Motif-Mediated Human Protein-Protein Interactions

Priyanka Madhu, Caroline Benz, Leandro Simonetti, Matthew J. Winters, Mythili S. Subbanna, Johanna Kliche, Lidia Gomez-Lucas, Hazem M. Kotb, Izabella Krystkowiak, Dmitri Segal, William T. P. Darling, Sven Larsen-Ledet, Maximilian Vieler, Ana Župančić, Aimiliani Konstantinou, , Ylva Ivarsson

The paper maps over 20,000 human protein-protein interactions mediated by short linear motifs using a peptide library screening approach.

bioRxiv · Jul 6, 2026 · PreprintBiochemistry

A proteome-wide dependency map of protein interaction motifs

Sara M. Ambjørn, Bob Meeusen, Johanna Kliche, Jinli Wang, Dimitriya Hristoforova Garvanska, Thomas Kruse, Blanca Lopez Mendez, Matthias Mann, Niels Mailand, Emil Peter Thrane Hertz, Norman E. Davey, Jakob Nilsson

The paper systematically assesses the function of short linear motifs (SLiMs) by mutating and screening them in human cells, identifying essential SLiMs for cell proliferation and uncovering novel classes and binding partners.

Nature Structural & Molecular Biology · Mar 1, 2026Peer-reviewedCell Biology

High-throughput discovery and deep characterization of cyclin-CDK docking motifs

Mihkel Örd, Matthew J. Winters, Mythili S. Subbanna, Natàlia de Martín Garrido, Victoria I. Cushing, Johanna Kliche, Caroline Benz, Ylva Ivarsson, Basil J. Greber, Peter M. Pryciak, Norman E. Davey

The paper identifies and characterizes cyclin-CDK docking motifs through high-throughput peptide binding assays and structural analysis, revealing a broader repertoire of motif types and binding mechanisms.

Nature Communications · Aug 15, 2025Peer-reviewedMolecular Biology