Target intelligence / Profile preview

Phosphoglycerate kinase (Cutibacterium acnes) (PGK)

Target
PGK
Molecular classification
Enzyme, Transferase, Kinase
01

Overview

Phosphoglycerate kinase (PGK) is a vital enzyme in the metabolic pathway of Cutibacterium acnes, the bacterium primarily responsible for the development of acne vulgaris (UniProt, 2024). It facilitates the transfer of a phosphate group from 1,3-bisphosphoglycerate to ADP, resulting in the formation of 3-phosphoglycerate and ATP, which is a critical step for energy production during glycolysis (NCBI, 2023). Because C. acnes thrives in the anaerobic environment of the skin's pilosebaceous units, its energy metabolism is a focal point for potential therapeutic intervention (PubMed, 2021). Targeting PGK offers a strategy to inhibit bacterial growth by starving the pathogen of its primary energy source. Although there are currently no FDA-approved drugs that specifically target C. acnes PGK, it is an active area of research for the development of next-generation, site-specific antimicrobials (Journal of Dermatological Science, 2022). Such inhibitors would ideally provide a narrow-spectrum approach to treating resistant acne while minimizing the impact on the broader human microbiome.

Other names
3-phosphoglycerate kinaseATP:3-phospho-D-glycerate 1-phosphotransferasePropionibacterium acnes phosphoglycerate kinasepgk
02

Mechanism of action

Inhibition of the glycolytic pathway leading to ATP depletion and bacterial growth arrest.

03

Biological functions

GlycolysisGluconeogenesisATP biosynthetic processCarbohydrate metabolism
04

Disease associations

InfectionAcne vulgaris
05

Safety considerations

Potential for off-target inhibition of human PGK1 or PGK2 enzymesPotential disruption of commensal skin microbiota

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