Wulf Blankenfeldt

Otto Hahn Str. 11
Dortmund, NW 44227, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 88 publications

S-Adenosyl-d-Methionine as a Non-Physiological Substrate for a Wide Range of SAM-Dependent Enzymes.

S-Adenosyl-d-Methionine as a Non-Physiological Substrate for a Wide Range of SAM-Dependent Enzymes.

Journal: Chembiochem : a European journal of chemical biology

Published: April 22, 2026

Synthesis and Activity-Based Protein Profiling Identifies Aldo-Keto Reductase 1C3 as Target Protein of Myxoglucamides.

Synthesis and Activity-Based Protein Profiling Identifies Aldo-Keto Reductase 1C3 as Target Protein of Myxoglucamides.

Journal: Angewandte Chemie (International ed. in English)

Published: April 11, 2026

Structural and Biochemical Characterization of the Diaminopimelate Epimerase DapF From Pseudomonas aeruginosa PA14.

Structural and Biochemical Characterization of the Diaminopimelate Epimerase DapF From Pseudomonas aeruginosa PA14.

Journal: Proteins

Published: February 19, 2026

An Imidazo[2,1-b][1,3,4]thiadiazole Derivative Inhibits the Virulence Factor α-Hemolysin by Blocking the Pullout of Its Stem Domain.

An Imidazo[2,1-b][1,3,4]thiadiazole Derivative Inhibits the Virulence Factor α-Hemolysin by Blocking the Pullout of Its Stem Domain.

Journal: ChemMedChem

Published: December 08, 2025

Microbial phenazines: biosynthesis, structural diversity, evolution, regulation, and biological significance.

Microbial phenazines: biosynthesis, structural diversity, evolution, regulation, and biological significance.

Journal: Microbiology and molecular biology reviews : MMBR

Published: October 01, 2025

From Bones to Bugs: Structure-Based Development of Raloxifene-Derived Pathoblockers That Inhibit Pyocyanin Production in Pseudomonas aeruginosa.

From Bones to Bugs: Structure-Based Development of Raloxifene-Derived Pathoblockers That Inhibit Pyocyanin Production in Pseudomonas aeruginosa.

Journal: Journal of medicinal chemistry

Published: March 29, 2025

Innovative zinc-binding inhibitors of Legionella pneumophila ProA reduce collagen and flagellin degradation, TLR5 evasion, and human lung tissue inflammation.

Innovative zinc-binding inhibitors of Legionella pneumophila ProA reduce collagen and flagellin degradation, TLR5 evasion, and human lung tissue inflammation.

Journal: European journal of medicinal chemistry

Published: January 23, 2025

AcrVIB1 inhibits CRISPR-Cas13b immunity by promoting unproductive crRNA binding accessible to RNase attack.

AcrVIB1 inhibits CRISPR-Cas13b immunity by promoting unproductive crRNA binding accessible to RNase attack.

Journal: Molecular cell

Published: October 01, 2024

Effect of pH and buffer on substrate binding and catalysis by cis-aconitate decarboxylase.

Effect of pH and buffer on substrate binding and catalysis by cis-aconitate decarboxylase.

Journal: Scientific reports

Published: September 30, 2024

Highly potent quinoxalinediones inhibit α-hemolysin and ameliorate Staphylococcus aureus lung infections.

Highly potent quinoxalinediones inhibit α-hemolysin and ameliorate Staphylococcus aureus lung infections.

Journal: Cell host & microbe

Published: August 23, 2024

Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase.

Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase.

Journal: Angewandte Chemie (International ed. in English)

Published: July 04, 2024

Substrate-Based Ligand Design for Phenazine Biosynthesis Enzyme PhzF.

Substrate-Based Ligand Design for Phenazine Biosynthesis Enzyme PhzF.

Journal: ChemMedChem

Published: June 14, 2024

Showing 1-12 of 88

Last Updated: 09/26/2026