Angel Luis Pey

Assistant Professor

Universidad de Granada

Spain

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About

Angel Luis Pey is an Assistant Professor at the University of Granada, Spain. His research focuses on the structural dynamics and biochemical mechanisms related to cancer, metabolic diseases, and protein stability. Recent publications explore various topics, including the therapeutic applications of nanobodies, enzyme activity regulation, and genotype-phenotype correlations in inherited diseases.

Articles (14)

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2025

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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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2022

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2022

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2022

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2022

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2022

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2021

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2021

Collaborators (13)

Petr Man

Institute of Microbiology

CZECH REPUBLIC

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Peter John O'Toole

Director of the Bioscience Technology Facility, and Head of Imaging and Cytometry

University of York

UNITED KINGDOM

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Rita Guzzi

Professore associato

University of Calabria

ITALY

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Rogelio Palomino-Morales

Assistant Professor

Universidad de Granada

SPAIN

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Miguel Xavier Fernandes

Senior Lecturer

Karlstad University

SWEDEN

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Mirco Dindo

Assistant Professor

University of Perugia

ITALY

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José L. Neira

Universidad de Zaragoza

SPAIN

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Eduardo Salido

Professor and Chair

Hospital Universitario de Canarias

SPAIN

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Milagros Medina

Universidad de Zaragoza

SPAIN

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Dmitry Loginov

CZECH REPUBLIC

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José Antonio Gómez Vidal

Universidad de Granada

SPAIN

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Barbara Cellini

University of Perugia

ITALY

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David Timson

University of Brighton

UNITED KINGDOM

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Angel Luis Pey

Research Interests

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Articles (14)

Thermodynamic versus kinetic basis for the high conformational stability of nanobodies for therapeutic applications

Phosphorylation of cytosolic hPGK1 affects protein stability and ligand binding: implications for its subcellular targeting in cancer

Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants

Counterintuitive structural and functional effects due to naturally occurring mutations targeting the active site of the disease‐associated NQO1 enzyme*

Phenotypic Modulation of Cancer-Associated Antioxidant NQO1 Activity by Post-Translational Modifications and the Natural Diversity of the Human Genome

Molecular Mechanisms, Genotype–Phenotype Correlations and Patient-Specific Treatments in Inherited Metabolic Diseases

Structural dynamics at the active site of the cancer‐associated flavoenzyme NQO1 probed by chemical modification with PMSF

Phosphorylation of Thr9 Affects the Folding Landscape of the N-Terminal Segment of Human AGT Enhancing Protein Aggregation of Disease-Causing Mutants

New salicylic acid derivatives, double inhibitors of glycolate oxidase and lactate dehydrogenase, as effective agents decreasing oxalate production

Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity-Making Mutations

Targeting HIF-1α Function in Cancer through the Chaperone Action of NQO1: Implications of Genetic Diversity of NQO1

A single evolutionarily divergent mutation determines the different FAD‐binding affinities of human and rat NQO1 due to site‐specific phosphorylation

Dimerization drives proper folding of human alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting

Structural basis of the pleiotropic and specific phenotypic consequences of missense mutations in the multifunctional NAD(P)H:quinone oxidoreductase 1 and their pharmacological rescue

Collaborators (13)

Petr Man

Peter John O'Toole

Rita Guzzi

Rogelio Palomino-Morales

Miguel Xavier Fernandes

Mirco Dindo

José L. Neira

Eduardo Salido

Milagros Medina

Dmitry Loginov

José Antonio Gómez Vidal

Barbara Cellini

David Timson

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