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Nature Communications|January 22, 2025
Chemical tools to define and manipulate interferon-inducible Ubl protease USP18Griffin J Davis, Anthony O Omole, Yejin Jung, et al.
Journal of the American Chemical Society|May 15, 2023
Covalent Inhibition by a Natural Product-Inspired Latent ElectrophileDavid P Byun, Jennifer Ritchie, Yejin Jung, et al.
Plos Pathogens|June 7, 2019
Covalent Plasmodium falciparum-selective proteasome inhibitors exhibit a low propensity for generating resistance in vitro and synergize with multiple antimalarial agentsBarbara H Stokes, Euna Yoo, James M Murithi, et al.
Protein Science : a Publication of the Protein Society|February 21, 2025
A robust fluorogenic substrate for chikungunya virus protease (nsP2) activitySparsh Makhaik, Wioletta Rut, Shruti Choudhary, et al.
Nature|February 12, 2016
Structure- and function-based design of Plasmodium-selective proteasome inhibitorsHao Li, Anthony J O'Donoghue, Wouter A van der Linden, et al.
Biorxiv : the Preprint Server for Biology|October 1, 2025
A Robust Fluorogenic Substrate for Chikungunya Virus Protease (nsP2) ActivitySparsh Makhaik, Wioletta Rut, Shruti Choudhary, et al.
ACS Chemical Biology|April 17, 2024
Discovery of a Tunable Heterocyclic Electrophile 4-Chloro-pyrazolopyridine That Defines a Unique Subset of Ligandable CysteinesHong-Rae Kim, David P Byun, Kalyani Thakur, et al.
Journal of the American Chemical Society|August 16, 2018
Defining the Determinants of Specificity of Plasmodium Proteasome InhibitorsEuna Yoo, Barbara H Stokes, Hanna de Jong, et al.
Bioconjugate Chemistry|July 4, 2018
Hyaluronic Acid Conjugates of TLR7/8 Agonists for Targeted Delivery to Secondary Lymphoid TissueEuna Yoo, Alex C D Salyer, Michael J H Brush, et al.
Journal of Medicinal Chemistry|September 6, 2014
Determinants of activity at human Toll-like receptors 7 and 8: quantitative structure-activity relationship (QSAR) of diverse heterocyclic scaffoldsEuna Yoo, Deepak B Salunke, Diptesh Sil, et al.
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