Ontology highlight
ABSTRACT:
SUBMITTER: Henneman L
PROVIDER: S-EPMC2946549 | biostudies-literature | 2010 Oct
REPOSITORIES: biostudies-literature
Henneman L L Schneiders M S MS Turkenburg M M Waterham H R HR
Journal of inherited metabolic disease 20100903 5
Mevalonate kinase deficiency (MKD) is an autoinflammatory disorder caused by mutations in the MVK gene resulting in decreased activity of the enzyme mevalonate kinase (MK). Although MK is required for biosynthesis of all isoprenoids, in MKD, in particular, the timely synthesis of geranylgeranyl pyrophosphate appears to be compromised. Because small guanosine triphosphatases (GTPases) depend on geranylgeranylation for their proper signaling function, we studied the effect of MK deficiency on gera ...[more]