Author

Péter Ábrányi‐Balogh

Budapest University of Technology and EconomicsORCID 0000-0002-9284-5160Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:drug response / drug discovery· 2 Approach:deep learning· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:protein structure· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

György Miklós KeserűiD· 2 shared Zoltán OrgovániD· 2 shared Christoph RademacheriD· 1 shared Dávid BajusziD· 1 shared Emma K. GrantiD· 1 shared Gitta SchlosseriD· 1 shared Iris A. BermejoiD· 1 shared István KolossváryiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersBiophysics

György Miklós KeserűORCID

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2 papers

Recent·Most cited

BiophysicsbioRxivPreprintOct 8, 2026

Efficient detection of cryptic pockets on challenging drug targets using MD-free co-vibrational modes

Tibor Viktor Szalai, Dávid Bajusz, Zoltán Orgován…·György Miklós Keserű

The paper identifies cryptic pockets on challenging drug targets using a fast MD-free method and validates them experimentally.

DOI 10.64898/2026.10.07.757394

humanprotein structure

Pharmacology & ToxicologyAngewandte Chemie International EditionPeer-reviewedNov 24, 2025

Covalent activation of the C-type lectin DC-SIGN

Jonathan Lefèbre, Maurice Besch, Noémi Csorba…·Christoph Rademacher

This paper identifies two covalent activators of DC-SIGN by screening a lysine-targeted electrophilic fragment library, revealing distinct mechanisms of activation through structural and functional analyses.

9 citations

proteomicsdeep learning