Target intelligence / Profile preview

Na+-translocating NADH-quinone reductase (Na+-NQR) (Na+-NQR)

Target
Na+-NQR
Molecular classification
Enzyme, Oxidoreductase, Transporter, Sodium pump
01

Overview

Na+-translocating NADH-quinone reductase (Na+-NQR) is a primary respiratory enzyme complex found in the inner membranes of various pathogenic bacteria, such as Vibrio cholerae and Neisseria gonorrhoeae (Source: PubMed PMID: 28961953). It catalyzes the transfer of electrons from NADH to ubiquinone, coupled to the translocation of sodium ions to generate a sodium motive force (SMF) (Source: PMC4054256). This SMF is essential for bacterial ATP synthesis, motility, and nutrient transport (Source: PubMed PMID: 24811130). Since Na+-NQR is absent in humans, who use a proton-pumping Complex I instead, it is a promising target for selective antibiotics (Source: MDPI Molecules 2023). Inhibitors like korormicin and clofazimine derivatives block this enzyme, leading to bacterial death through energy depletion and reactive oxygen species production (Source: Loyola eCommons 2022). The enzyme consists of six subunits (NqrA-F) and utilizes multiple cofactors, including FAD and FMN, to facilitate electron flow (Source: PMC10331415). Targeting the unique sodium-pumping mechanism provides a strategy to combat multi-drug resistant pathogens without affecting host mitochondrial function.

Other names
Na+-pumping NADH:ubiquinone oxidoreductaseNQR complexNADH:ubiquinone oxidoreductase (Na+-translocating)Respiratory sodium pump
02

Mechanism of action

Inhibition of the respiratory enzyme activity, preventing the generation of a sodium motive force required for bacterial ATP synthesis and motility, often leading to the production of lethal reactive oxygen species (Source: PubMed PMID: 28961953).

03

Biological functions

Energy metabolismSodium ion transportRespiratory electron transport chainGeneration of sodium motive forceATP synthesisBacterial motility
04

Disease associations

InfectionCholeraGonorrheaChlamydial infection
05

Safety considerations

Potential disruption of beneficial commensal microbiotaDevelopment of antimicrobial resistance (e.g., NqrB mutations)Limited spectrum of activity
06

Interacting drugs

Korormicin

5 more in the full profile.

07

Biomarkers

Bacterial loadNQR enzyme activityReactive oxygen species levels

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