Entity Details

Primary name AMACR_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UHK6
EntryNameAMACR_HUMAN
FullNameAlpha-methylacyl-CoA racemase
TaxID9606
Evidenceevidence at protein level
Length382
SequenceStatuscomplete
DateCreated2001-04-27
DateModified2021-06-02

Ontological Relatives

GenesAMACR

GO terms

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GOName
GO:0005102 signaling receptor binding
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005777 peroxisome
GO:0005782 peroxisomal matrix
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0006699 bile acid biosynthetic process
GO:0008104 protein localization
GO:0008111 alpha-methylacyl-CoA racemase activity
GO:0008206 bile acid metabolic process
GO:0008410 CoA-transferase activity
GO:0033540 fatty acid beta-oxidation using acyl-CoA oxidase
GO:0043231 intracellular membrane-bounded organelle

Subcellular Location

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Subcellular Location
Mitochondrion
Peroxisome

Domains

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DomainNameCategoryType
IPR003673 CoA-transferase family IIIFamilyFamily
IPR023606 CoA-transferase family III domain 1 superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
214950 OMIMCongenital bile acid synthesis defect 4 (CBAS4)A disorder characterized by the presence of trihydroxycoprostanic acid in the bile and absence of cholic acid. Patients manifest neonatal jaundice, intrahepatic cholestasis and bile duct deficiency. The disease is caused by variants affecting the gene represented in this entry.
614307 OMIMAlpha-methylacyl-CoA racemase deficiency (AMACRD)A rare autosomal recessive peroxisomal disorder characterized by elevated plasma concentrations of pristanic acid C27-bile-acid intermediates, and adult onset of variable neurodegenerative symptoms affecting the central and peripheral nervous systems. Features may include seizures, visual failure, sensorimotor neuropathy, spasticity, migraine, and white matter hyperintensities on brain imaging. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
AMACR_HUMANPEX5_HUMANBioGRID20178365 details