M. Acebrón-García-de-Eulate

Development of Inhibitors of SAICAR Synthetase (PurC) from Mycobacterium abscessus Using a Fragment-Based Approach.

T. Blundell, C. Abell, R. Floto, 2022, ACS infectious diseases.

HARP: a database of structural impacts of systematic missense mutations in drug targets of Mycobacterium leprae

Marcin J. Skwark, Ali F. Alsulami, T. Blundell, 2020, Computational and structural biotechnology journal.

Discovery of Novel Inhibitors of Uridine Diphosphate-N-Acetylenolpyruvylglucosamine Reductase (MurB) from Pseudomonas aeruginosa, an Opportunistic Infectious Agent Causing Death in Cystic Fibrosis Patients.

T. Blundell, C. Abell, A. Coyne, 2022, Journal of medicinal chemistry.

Strategies for drug target identification in Mycobacterium leprae.

T. Blundell, M. Acebrón-García-de-Eulate, Sundeep Chaitanya Vedithi, 2021, Drug discovery today.

Structure-Guided Computational Approaches to Unravel Druggable Proteomic Landscape of Mycobacterium leprae

T. Blundell, S. Malhotra, P. Torres, 2021, Frontiers in Molecular Biosciences.

Structure-Based Design, Synthesis, and Characterization of the First Irreversible Inhibitor of Focal Adhesion Kinase.

John C. Dawson, X. Coumoul, M. Frame, 2018, ACS chemical biology.

Mycobacterial OtsA Structures Unveil Substrate Preference Mechanism and Allosteric Regulation by 2-Oxoglutarate and 2-Phosphoglycerate

T. Blundell, Vítor Mendes, M. Dias, 2019, mBio.