Mitochondrial respiratory chain complex III assembly gene defect (Q107591): Difference between revisions
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Complexo III é quando o ciclo Q contribui para o gradiente de prótons por uma absorção/liberação assimétrica de prótons. Dois elétrons são removidos de QH2 no local QO e sequencialmente transferidos para duas moléculas de citocromo C, um transportador de elétrons solúvel em água localizado dentro do espaço intermembranar. Este diagnóstico é pelo defeito do gene de montagem. | |||
| description / en | description / en | ||
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. | |||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_400611280 |
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| English | 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. |
