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Structure of human mitochondrial trifunctional protein, octamerStructure of human mitochondrial trifunctional protein, octamer
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Structural highlights
DiseaseECHA_HUMAN Mitochondrial trifunctional protein deficiency;Acute fatty liver of pregnancy;Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. FunctionECHA_HUMAN Bifunctional subunit. Contents |