Aminoacylase 1 Active Protein | ACY1 active protein

Aminoacylase 1 Protein, Mouse, Recombinant (His Tag)

Cat. Num. AAA8122457

• Gene Names: Acy1; Acy-1; 1110014J22Rik
• Purity: >95% as determined by SDS-PAGE
• Synonyms: Aminoacylase 1; Aminoacylase 1 Protein; Mouse; Recombinant (His Tag); Mouse ACY1/Aminoacylase-1 Protein (His Tag); 1110014J22Rik Protein; Acy-1 Protein; aminoacylase 1; ACY1 active protein

• Host: HEK293 Cells
• Purity/Purification: >95% as determined by SDS-PAGE
• Form/Format: Lyophilized from sterile PBS, pH7.4. Normally 5%-8% trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization. Please refer to the specific buffer information in the hard copy of CoA.
• Sequence: Met1-Ser408

• Species: Mouse
• Activity: Measured by its ability to cleave N-acetyl-L-Methione (Ac-Met). The specific activity is >4,000pmoles/min/ug.
• Endotoxin: <1.0EU per ug of the protein as determined by the LAL method
• Predicted N Terminal: Gln 18
• Tag: C-His
• Protein Construction: A DNA sequence encoding the mouse ACY1 (Q99JW2)(Met 1-Ser 408) was expressed with a C-terminal polyhistidine tag.
• Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.
• Preparation and Storage: Samples are stable for up to twelve months from date of receipt at -20 degree C to -80 degree C. Store it under sterile conditions at -20 degree C to -80 degree C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.; In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature. Bulk packages of recombinant proteins are provided as frozen liquid.; They are shipped out with blue ice.

SDS-Page

Related Product Information for ACY1 active protein

Background: Aminoacylase 1 (ACY1), a metalloenzyme that removes amide-linked ACY1 groups from amino acids and may play a role in regulating responses to oxidative stress. Both the C-terminal fragment found in the two-hybrid screen and full-length ACY1 co-immunoprecipitate with SphK1. Though both C-terminal and full-length proteins slightly reduce SphK1 activity measured in vitro, the C-terminal fragment inhibits while full-length ACY1 potentiates the effects of SphK1 on proliferation and apoptosis. It suggested that ACY1 physically interacts with SphK1 and may influence its physiological functions. As a homodimeric zinc-binding enzyme, Aminoacylase 1 catalyzes the hydrolysis of N alpha-acylated amino acids. Deficiency of Aminoacylase 1 due to mutations in the Aminoacylase 1 (ACY1) gene follows an autosomal-recessive trait of inheritance and is characterized by accumulation of N-acetyl amino acids in the urine.

References

Sommer A, et al. (2011) The molecular basis of aminoacylase 1 deficiency. Biochim Biophys Acta. 1812(6): 685-90.Maceyka M, et al. (2004) Aminoacylase 1 is a sphingosine kinase 1-interacting protein. FEBS Lett. 568(1-3): 30-4.Cook RM, et al.(1993) Human aminoacylase-1. Cloning, sequence, and expression analysis of a chromosome 3p21 gene inactivated in small cell lung cancer. J Biol Chem. 268(23): 17010-7.

NCBI and Uniprot Product Information

• NCBI GI #: 449784892
• NCBI GeneID: 109652
• NCBI Accession #: NP_001263371.1
• NCBI GenBank Nucleotide #: NM_001276442.1
• UniProt Accession #: Q99JW2; Q9CR15
• Molecular Weight: 45,781 Da
• NCBI Official Full Name: aminoacylase-1
• NCBI Official Synonym Full Names: aminoacylase 1
• NCBI Official Symbol: Acy1
• NCBI Official Synonym Symbols: Acy-1; 1110014J22Rik
• NCBI Protein Information: aminoacylase-1
• UniProt Protein Name: Aminoacylase-1
• Protein Family: Aminoacylase
• UniProt Gene Name: Acy1
• UniProt Synonym Gene Names: ACY-1
• UniProt Entry Name: ACY1_MOUSE

Uniprot Description

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 syringomyelia, 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 3.5.1.14; Hydrolase

Molecular Function: aminoacylase activity; zinc ion binding

Biological Process: peptide catabolic process; proteolysis