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DprE1 Is a Vulnerable Tuberculosis Drug Target Due to Its Cell Wall Localization
- Publisher :
- American Chemical Society
-
Abstract
- The flavo-enzyme DprE1 catalyzes a key epimerization step in the decaprenyl-phosphoryl d-arabinose (DPA) pathway, which is essential for mycobacterial cell wall biogenesis and targeted by several new tuberculosis drug candidates. Here, using differential radiolabeling with DPA precursors and high-resolution fluorescence microscopy, we disclose the unexpected extracytoplasmic localization of DprE1 and periplasmic synthesis of DPA. Collectively, this explains the vulnerability of DprE1 and the remarkable potency of the best inhibitors.
- Subjects :
- Drug
Tuberculosis
media_common.quotation_subject
Drug target
Antitubercular Agents
Biology
Biochemistry
Mycobacterial cell
Cell wall
Bacterial Proteins
Cell Wall
Fluorescence microscope
medicine
Humans
media_common
fungi
General Medicine
Periplasmic space
Mycobacterium tuberculosis
medicine.disease
3. Good health
Alcohol Oxidoreductases
Molecular Medicine
Biogenesis
Subjects
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....f63164c0af086c942318eef104bf68ec