Methylglutaconyl-CoA hydratase

AUH
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAUH, AU RNA binding protein/enoyl-CoA hydratase, Methylglutaconyl-CoA hydratase, AU RNA binding methylglutaconyl-CoA hydratase
External IDsOMIM: 600529; MGI: 1338011; HomoloGene: 1284; GeneCards: AUH; OMA:AUH - orthologs
Orthologs
SpeciesHumanMouse
Entrez

549

11992

Ensembl

ENSG00000148090

ENSMUSG00000021460

UniProt

Q13825

Q9JLZ3

RefSeq (mRNA)

NM_001306190
NM_001698
NM_001351431
NM_001351432
NM_001351433

NM_016709

RefSeq (protein)

NP_001293119
NP_001689
NP_001338360
NP_001338361
NP_001338362

NP_057918

Location (UCSC)Chr 9: 91.21 – 91.36 MbChr 13: 52.99 – 53.08 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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. Mutations of this gene have been found to cause a disease called 3-Methylglutaconic Acuduria Type 1.