Methylglutaconyl-CoA hydratase
Protein-coding gene in the species Homo sapiens / From Wikipedia, the free encyclopedia
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3-Methylglutaconyl-CoA hydratase, also known as MG-CoA hydratase and AUH, is an enzyme (EC 4.2.1.18) encoded by the AUH gene on chromosome 19. It is a member of the enoyl-CoA hydratase/isomerase superfamily, but it is the only member of that family that is able to bind to RNA. Not only does it bind to RNA, AUH has also been observed to be involved in the metabolic enzymatic activity, making it a dual-role protein.[5] Mutations of this gene have been found to cause a disease called 3-Methylglutaconic Acuduria Type 1.[6]
Quick Facts AUH, Available structures ...
AUH | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | AUH, AU RNA binding protein/enoyl-CoA hydratase, Methylglutaconyl-CoA hydratase, AU RNA binding methylglutaconyl-CoA hydratase | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 600529; MGI: 1338011; HomoloGene: 1284; GeneCards: AUH; OMA:AUH - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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