Mitochondrial respiratory chain complex III structural subunit gene defect (Q107590): 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 com defeito do gene da subunidade estrutural. | |||||||||||||||
| 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 structural subunit gene defect. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1696588973 / rank | |||||||||||||||
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CID11:ID_1696588973 | |||||||||||||||
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dki-india-ID_1696588973 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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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 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. |
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CID11:ID_1696588973
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dki-india-ID_1696588973
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Concluído
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16 August 2026
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