Mitochondrial respiratory chain complex III assembly gene defect (Q107591): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
16 August 2026
| |||||||||||||||
| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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. |
Statements
CID11:ID_400611280
0 references
dki-india-ID_400611280
0 references
Concluído
0 references
16 August 2026
0 references
