Mitochondrial respiratory chain complex III structural subunit gene defect (Q107590): 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 structural subunit gene defect.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1696588973 |
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| English | Mitochondrial respiratory chain complex III structural subunit 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 structural subunit gene defect. |
