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BRENDA support

Literature summary for 7.1.1.5 extracted from

  • Moosa, A.; Lamprecht, D.A.; Arora, K.; Barry, C.E.; Boshoff, H.I.M.; Ioerger, T.R.; Steyn, A.J.C.; Mizrahi, V.; Warner, D.F.
    Susceptibility of Mycobacterium tuberculosis cytochrome bd oxidase mutants to compounds targeting the terminal respiratory oxidase, cytochrome c (2017), Antimicrob. Agents Chemother., 61, e01338 .
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Mycobacterium tuberculosis L7N662 and O06139 L7N662 i.e. subunit cydA, O06139 i.e. subunit cydB
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Mycobacterium tuberculosis H37Rv L7N662 and O06139 L7N662 i.e. subunit cydA, O06139 i.e. subunit cydB
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General Information

General Information Comment Organism
physiological function mutants lacking subunits cydA and cydAB are hypersusceptible to compounds targeting the mycobacterial bc1 menaquinol cytochrome c oxidoreductase and exhibit bioenergetic profiles indistinguishable from strains deficient in the ABC-type transporter, CydDC, predicted to be essential for cytochrome bd assembly Mycobacterium tuberculosis