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Literature summary for 1.5.1.3 extracted from

  • Kaur, S.; Bhattacharyya, R.; Banerjee, D.
    Hydrochlorothiazide and indapamide bind the NADPH binding site of bacterial dihydrofolate reductase results of an in-silico study and their implications (2020), In Silico Pharmacol., 8, 005 .
    View publication on PubMedView publication on EuropePMC

Crystallization (Commentary)

Crystallization (Comment) Organism
modeling of complexes with inhibitors hydrochlorothiazide and indapamide. Compared to the DHFR-ethacrynic acid complex, DHFR-sulphadiazine, DHFR-indapamide, and DHFR-hydrochlorothiazide complexes have higher negative binding energies. The compounds may act similar to antibiotics from the perspective of binding with DHFR Escherichia coli

Inhibitors

Inhibitors Comment Organism Structure
hydrochlorothiazide sulfonamide diuretic, able to bind to DHFR Escherichia coli
indapamide sulfonamide diuretic, able to bind to DHFR Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli P0ABQ4
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