James A. Brannigan

York, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Direct SpoIIQ-SpoIIIAH interaction is dispensable for sporulation in Bacillus subtilis.

Direct SpoIIQ-SpoIIIAH interaction is dispensable for sporulation in Bacillus subtilis.

Journal: The Journal of biological chemistry

Published: October 01, 2025

Chemical genetics reveals Leishmania KKT2 and CRK9 kinase activity is required for cell cycle progression.

Chemical genetics reveals Leishmania KKT2 and CRK9 kinase activity is required for cell cycle progression.

Journal: PLoS pathogens

Published: September 15, 2025

Structure and activity of the essential UCH family deubiquitinase DUB16 from Leishmania donovani.

Structure and activity of the essential UCH family deubiquitinase DUB16 from Leishmania donovani.

Journal: The Biochemical journal

Published: March 06, 2025

Drug discovery in leishmaniasis using protein lipidation as a target.

Drug discovery in leishmaniasis using protein lipidation as a target.

Journal: Biophysical reviews

Published: August 04, 2021

Novel Thienopyrimidine Inhibitors of Leishmania N-Myristoyltransferase with On-Target Activity in Intracellular Amastigotes.

Novel Thienopyrimidine Inhibitors of Leishmania N-Myristoyltransferase with On-Target Activity in Intracellular Amastigotes.

Journal: Journal of medicinal chemistry

Published: June 25, 2020

Crystal structures of the GH18 domain of the bifunctional peroxiredoxin-chitinase CotE from Clostridium difficile.

Crystal structures of the GH18 domain of the bifunctional peroxiredoxin-chitinase CotE from Clostridium difficile.

Journal: Acta crystallographica. Section F, Structural biology communications

Published: March 19, 2020

Site-selective C-C modification of proteins at neutral pH using organocatalyst-mediated cross aldol ligations.

Site-selective C-C modification of proteins at neutral pH using organocatalyst-mediated cross aldol ligations.

Journal: Chemical science

Published: April 09, 2018

Fragment-derived inhibitors of human N-myristoyltransferase block capsid assembly and replication of the common cold virus.

Fragment-derived inhibitors of human N-myristoyltransferase block capsid assembly and replication of the common cold virus.

Journal: Nature chemistry

Published: August 14, 2017

Structure-guided optimization of quinoline inhibitors of Plasmodium N-myristoyltransferase.

Structure-guided optimization of quinoline inhibitors of Plasmodium N-myristoyltransferase.

Journal: MedChemComm

Published: September 20, 2016

Discovery of high affinity inhibitors of Leishmania donovani N-myristoyltransferase.

Discovery of high affinity inhibitors of Leishmania donovani N-myristoyltransferase.

Journal: MedChemComm

Published: June 06, 2015

Discovery of pyridyl-based inhibitors of Plasmodium falciparum N-myristoyltransferase.

Discovery of pyridyl-based inhibitors of Plasmodium falciparum N-myristoyltransferase.

Journal: MedChemComm

Published: June 06, 2015

Structure mediation in substrate binding and post-translational processing of penicillin acylases: Information from mutant structures of Kluyvera citrophila penicillin G acylase.

Structure mediation in substrate binding and post-translational processing of penicillin acylases: Information from mutant structures of Kluyvera citrophila penicillin G acylase.

Journal: Protein science : a publication of the Protein Society

Published: May 08, 2015

Showing 1-12 of 26

Last Updated: 09/26/2026