Author

Emma K. Punch

The Francis Crick InstituteORCID 0000-0002-5477-6619Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:protein structure· 1 Research Focus:protein structure prediction· 1 Assay:structural biology· 1

Frequent Co-Authors

Peter CherepanoviD· 2 shared Alexander B. TayloriD· 1 shared Andrew P. HinckiD· 1 shared Caroline S. HilliD· 1 shared Chang‐Hyeock ByeoniD· 1 shared Cynthia S. HinckiD· 1 shared Daniel J. BernardiD· 1 shared Fernando López‐CasillasiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersMicrobiology

Peter CherepanovORCID

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2 papers

Recent·Most cited

HTLV-1 intasome recruits the PP2A-B56 holoenzyme and restricts its phosphatase activity

Jordan James Minnell, Emma K. Punch, Teresa Vanzo, Roghaiyeh Safari, Nora Cronin, P.G. Cherepanov, Goedele N. Maertens

The paper shows HTLV-1 integrase recruits PP2A-B56 holoenzyme, structurally inhibiting its phosphatase activity without affecting infection.

bioRxiv · May 4, 2026 · PreprintMicrobiology

Structures of TGF-beta with betaglycan and the signaling receptors reveal the mechanism whereby betaglycan potentiates receptor complex assembly and signaling

Łukasz Wieteska, Alexander B. Taylor, Emma K. Punch, Jonathan A. Coleman, Isabella O. Conway, Yeu‐Farn Lin, Chang‐Hyeock Byeon, Cynthia S. Hinck, Troy C. Krzysiak, Rieko Ishima, Fernando López‐Casillas, Peter Cherepanov, Daniel J. Bernard, Caroline S. Hill, Andrew P. Hinck

This study determines the structure of TGF-beta bound to betaglycan and its signaling receptors, revealing mechanisms of ligand selectivity and signal potentiation.

Nature Communications · Feb 26, 2025Peer-reviewedBiophysics