| Aminoacylase-1 ELISA Kit|
|Also known as Aminoacylase-1 (ACY-1) (N-acyl-L-amino-acid amidohydrolase). |
ACY1: Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). Defects in ACY1 are the cause of aminoacylase-1 deficiency (ACY1D). ACY1D results in a metabolic disorder manifesting with encephalopathy, unspecific psychomotor delay, psychomotor delay with atrophy of the vermis and syringo
myelia, marked muscular hypotonia or normal clinical features. Epileptic seizures are a frequent feature. All affected individuals exhibit markedly increased urinary excretion of several N-acetylated amino acids. Belongs to the peptidase M20A family.
Protein type: Amino Acid Metabolism - arginine and proline; EC 18.104.22.168; Hydrolase
Molecular Function: aminoacylase activity; zinc ion binding
Biological Process: peptide catabolic process; proteolysis
| Acy1 ELISA Kit|