9hzl | pdb_00009hzl
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High resolution cryo-EM structure of human complex III in mitochondria
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Structural highlights
DiseaseQCR8_HUMAN Isolated CoQ-cytochrome C reductase deficiency. The disease is caused by mutations affecting the gene represented in this entry. FunctionQCR8_HUMAN This is a component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is part of the mitochondrial respiratory chain. This subunit, together with cytochrome b, binds to ubiquinone. Contents | ||||||||||||||||||||
This page was last modified 07:23, 12 November 2025.