Author

Ashley J. Ovens

St Vincents Institute of Medical ResearchORCID 0000-0001-5711-6555Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:protein folding & dynamics· 2 Approach:biophysical modeling· 1 Assay:protein structure· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Benjamin R. Turner· 2 shared Christopher G. LangendorfiD· 2 shared Geoff X.Y. Zhang· 2 shared John W. ScottiD· 2 shared Kei SakamotoiD· 2 shared Meiqi Cao· 2 shared Muhammad N.H. Khabib· 2 shared Alex Bernard AddinsalliD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersImmunology

Benjamin R. Turner

Mutual co-authors in cluster

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3 papers

Recent·Most cited

ImmunologybioRxivPreprintAug 20, 2026

Leukocyte Immunoglobulin-Like Receptor B1 and its Interactions with Human Leukocyte Antigens

Geoff X.Y. Zhang, Jia Quyen Truong, Lucy Sullivan…·Christopher G. Langendorf

This study investigates LILRB1-HLA-I interactions, showing differential binding preferences across HLA-I allotypes and providing structural insights relevant to immunotherapy.

DOI 10.64898/2026.08.16.745109

humanprotein structure

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BiochemistrybioRxivPreprintAug 19, 2026

Fine tuning energy metabolism in skeletal muscle: Discovery of a novel autoinhibitory mechanism in the N-terminal extension of AMPKγ3

Ashley J. Ovens, Muhammad N.H. Khabib, Dingyi Yu…·Christopher G. Langendorf

This study identifies an autoinhibitory mechanism in the N-terminal extension of AMPKγ3 that regulates basal activity in skeletal muscle, offering a target for T2DM therapies.

DOI 10.64898/2026.08.16.744724

humanproteomics

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BiochemistryScience AdvancesPeer-reviewedAug 22, 2025

Mechanism and cellular actions of the potent AMPK inhibitor BAY-3827

Conchita Fraguas Bringas, Mohd Syed Ahangar, Joyceline Cuenco…·Kei Sakamoto

This paper describes the mechanism and cellular effects of the potent AMPK inhibitor BAY-3827, showing it selectively blocks AMPK-dependent functions.

12 citations

experimental assay

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