Adenosine Deaminase Like Protein (ADAL)

Adenosine Deaminase Like Protein (ADAL)
ADAL, Belongs to the adenosine and AMP deaminases family. Putative nucleoside deaminase. May catalyze the hydrolytic deamination of adenosine or some similar substrate and play a role in purine metabolism. Adenosine Deaminase (ADA) is a cytosolic enzyme, which has been the object of considerable interest, mainly because in human a congenital defect in the enzyme causes severe combined immunodeficiency disease (SCID). ADA participates in the purine metabolism where it degrades either adenosine or 2’-deoxyadenosine producing inosine or 2’- deoxyinosine, respectively. Further metabolisation of these deaminated nucleosides leads to hypoxanthine, which can be either transformed into uric acid by xanthine oxidase or salvaged into mononucleotides by the action of hypoxanthine-guanine phosphoribosyl-transferase.

Organism species: Homo sapiens (Human)

Organism species: Mus musculus (Mouse)