Mitochondrial respiratory chain complex III assembly gene defect (Q107591): Difference between revisions

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Revision as of 14:35, 17 August 2026

Complex III is when the Q-cycle contributes to the proton gradient by an asymmetric absorption/release of protons. Two electrons are removed from QH2 at the QO site and sequentially transferred to two molecules of cytochrome c, a water-soluble electron carrier located within the intermembrane space. This diagnosis is with assembly gene defect.
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ID_400611280
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    Mitochondrial respiratory chain complex III assembly gene defect
    Complex III is when the Q-cycle contributes to the proton gradient by an asymmetric absorption/release of protons. Two electrons are removed from QH2 at the QO site and sequentially transferred to two molecules of cytochrome c, a water-soluble electron carrier located within the intermembrane space. This diagnosis is with assembly gene defect.

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