Function
Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis.
Biological Context
Subcellular Location: Cytoplasm
Disease Association: Adenine phosphoribosyltransferase deficiency (APRTD) : An enzymatic deficiency that can lead to urolithiasis and renal failure. Patients have 2,8-dihydroxyadenine (DHA) urinary stones. [The disease is caused by variants affecting the gene represented in this entry]
Pathway: Purine metabolism; AMP biosynthesis via salvage pathway; AMP from adenine: step 1/1
Product Specifications
Recombinant Human Adenine phosphoribosyltransferase (APRT) is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 1-180aa, with N-terminal GST-tagged tag, molecular weight 46.5kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications. Explore more Enzyme proteins →
