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mutant MTRR:MTR(cob(II)alamin) [cytosol]
Stable Identifier
R-HSA-9013254
Type
Complex
Species
Homo sapiens
Compartment
cytosol
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Defects in vitamin and cofactor metabolism (Homo sapiens)
Defects in cobalamin (B12) metabolism (Homo sapiens)
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE (Homo sapiens)
Defective MTRR does not convert cob(II)alamin to MeCbl (Homo sapiens)
mutant MTRR:MTR(cob(II)alamin) [cytosol] (Homo sapiens)
Participants
components
MTR:Zn2+:cob(II)alamin [cytosol] (Homo sapiens)
mutant MTRR:FMN:FAD [cytosol] (Homo sapiens)
Participant Of
input
Defective MTRR does not convert cob(II)alamin to MeCbl
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