R224P BCKDK dimer [mitochondrial matrix]

Stable Identifier
R-HSA-9912535
Type
Complex
Species
Homo sapiens
Compartment
mitochondrial matrix
Locations in the PathwayBrowser
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Participants
components
Participates
as a member of
Disease
Name Identifier Synonyms
branched-chain keto acid dehydrogenase kinase deficiency DOID:0090126 BCKDKD, BCKDK deficiency, autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
Cross References
Mondo
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