EC Number   |
General Information |
Reference |
|---|
    4.2.1.18 | malfunction |
enzyme deficiency, due to homozygous deletion of exons 1-3 within the AUH gene, leads to 3-methylglutaconic aciduria type I with phenotypic heterogeneity, e.g. learning disability, attention deficit-hyperactivity and early onset subclinical leukoencephalopathy or severe expressive speech delay and delay in speech sound development with normal cognitive functions, overview |
716241 |
| 4.2.1.18 | physiological function |
at4g16800 knockout plants subjected to dark-induced carbon starvation, display accelerated senescence in their rosette leaves as compared with control plants, and a marked increase in the accumulation of free and total leucine, isoleucine and valine. The seeds of the at4g16800 mutant show a similar accumulation of free branched-chain amino acids |
748959 |
| 4.2.1.18 | physiological function |
the depletion of 3-MGCoA-H by RNAi affects minimally the proliferation of both insect and mammalian bloodstream forms. An excess of leucine in the culture medium causes growth defects in cells depleted of 3-MGCoA-H, which can be reestablished by mevalonate. Procyclics depleted of the 3-MGCoA-H present reduced levels of synthesized steroids relative to cholesterol that is scavenged by the parasite |
-, 748625 |
