Georgios Pantouris

Assistant Professor

University of the Pacific

United States

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Dr. Georgios Pantouris is an Assistant Professor at the University of the Pacific, USA. His research focuses on the conformational flexibility of proteins, molecular recognition in protein-ligand complexes, and the implications of small-molecule inhibitors in immune responses. Recent publications include investigations into the mechanisms of the tautomerase superfamily and the characterization of the macrophage migration inhibitory factor (MIF).

Articles (17)

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2024

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2021

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2021

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2020

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2020

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2020

Collaborators (2)

Seamas Donnelly

Professor of Medicine

Trinity College Dublin

IRELAND

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Charles McCallum

Professor

University of the Pacific

UNITED STATES

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Georgios Pantouris

Research Interests

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Articles (17)

A small-molecule allele-selective transcriptional inhibitor of the MIF immune susceptibility locus

The C-terminal Region of D-DT Regulates Molecular Recognition for Protein-Ligand Complexes.

Iguratimod, an allosteric inhibitor of macrophage migration inhibitory factor (MIF), prevents mortality and oxidative stress in a murine model of acetaminophen overdose.

Conformational Flexibility of the C-Terminal Region Influences Distal Active Site Residues Across the Tautomerase Superfamily

Analysis of CD74 Occurrence in Oncogenic Fusion Proteins.

Protocol for purification and enzymatic characterization of members of the human macrophage migration inhibitory factor superfamily.

Hands-On Methods to Educate High School Students about Cancer Research

A novel enzymatic assay for the identification of 4-hydroxyphenylpyruvate dioxygenase modulators.

Underrepresented Impurities in 4-Hydroxyphenylpyruvate Affect the Catalytic Activity of Multiple Enzymes.

2,5-Pyridinedicarboxylic acid is a bioactive and highly selective inhibitor of D-dopachrome tautomerase.

Ligand-induced conformational changes enable intersubunit communications in D-dopachrome tautomerase.

A Cysteine Variant at an Allosteric Site Alters MIF Dynamics and Biological Function in Homo- and Heterotrimeric Assemblies.

MIF but not MIF-2 recruits inflammatory macrophages in an experimental polymicrobial sepsis model.

The N-terminus of MIF regulates the dynamic profile of residues involved in CD74 activation.

The N-terminal length and side-chain composition of CXCL13 affect crystallization, structure and functional activity.

An allosteric site on MKP5 reveals a strategy for small-molecule inhibition.

Regulation of MIF Enzymatic Activity by an Allosteric Site at the Central Solvent Channel.

Collaborators (2)

Seamas Donnelly

Charles McCallum

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