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Literature summary extracted from

  • De Vet, E.C.J.M.; Ijlst, L.; Oostheim, W.; Wanders, R.J.A.; Van Den Bosch, H.
    Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency (1998), J. Biol. Chem., 273, 10296-10301.
    View publication on PubMed

Application

EC Number Application Comment Organism
2.5.1.26 medicine enzyme levels are strongly reduced in fibroblasts derived from Zellweger syndrome and rhizomelic chondrodysplasia punctata patients Homo sapiens

Protein Variants

EC Number Protein Variants Comment Organism
2.5.1.26 R419H inactive enzyme Homo sapiens

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.5.1.26 Phenylglyoxal inactivation Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
2.5.1.26 Homo sapiens
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