- GMP 1.1
- AMP 1.2
- Guanine 2.1
- Adenine 2.2
- Salvage 3
- Disorders 4
- Pharmacotherapy 5
- See also 6
- External links 7
Purines are biologically synthesized as glutamine and water to 5'-phosphoribosylamine, glutamate, and pyrophosphate - catalyzed by pyrophosphate amidotransferase, which is activated by PRPP and inhibited by AMP, GMP and IMP.
Inosine monophosphate is synthesized on a pre-existing ribose-phosphate through a complex pathway (as shown in the figure on the right). The source of the carbon and nitrogen atoms of the purine ring, 5 and 4 respectively, come from multiple sources. The amino acid glycine contributes all its carbon (2) and nitrogen (1) atoms, with additional nitrogen atoms from glutamine (2) and aspartic acid (1), and additional carbon atoms from formyl groups (2), which are transferred from the coenzyme tetrahydrofolate as 10-formyltetrahydrofolate, and a carbon atom from bicarbonate (1). Formyl groups build carbon-2 and carbon-8 in the purine ring system, which are the ones acting as bridges between two nitrogen atoms.
- IMP dehydrogenase converts IMP into XMP
- GMP synthase converts XMP into GMP
- GMP reductase converts GMP back into IMP
- GMP reductase converts IMP
- adenylosuccinate synthase converts IMP to adenylosuccinate
- adenylosuccinate lyase converts adenylosuccinate into AMP
- AMP deaminase converts AMP back into IMP
Purines are metabolised by several enzymes:
- A nuclease frees the nucleotide
- A nucleotidase creates guanosine
- Purine nucleoside phosphorylase converts guanosine to guanine
- Guanase converts guanine to xanthine
- Xanthine oxidase (a form of xanthine oxidoreductase) catalyzes the oxidation of xanthine to uric acid
- A nuclease frees the nucleotide
- Purine nucleoside phosphorylase acts upon inosine to create hypoxanthine
- Xanthine oxidoreductase catalyzes the biotransformation of hypoxanthine to xanthine
- Xanthine oxidoreductase acts upon xanthine to create uric acid
Purines from turnover of nucleic acids (or from food) can also be salvaged and reused in new nucleotides.
- The enzyme adenine phosphoribosyltransferase (APRT) salvages adenine.
- The enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT) salvages guanine and hypoxanthine. (Genetic deficiency of HGPRT causes Lesch-Nyhan syndrome.)
When a defective gene causes gaps to appear in the metabolic recycling process for purines and pyrimidines, these chemicals are not metabolised properly, and adults or children can suffer from any one of twenty-eight hereditary disorders, possibly some more as yet unknown. Symptoms can include gout, anaemia, epilepsy, delayed development, deafness, compulsive self-biting, kidney failure or stones, or loss of immunity.
Modulation of purine metabolism has pharmacotherapeutic value.
Purine synthesis inhibitors inhibit the proliferation of cells, especially autoimmune disease such as rheumatoid arthritis or inflammatory bowel disease such as Crohn's disease and ulcerative colitis.
Allopurinol is a drug that inhibits the enzyme xanthine oxidoreductase and, thus, lowers the level of uric acid in the body. This may be useful in the treatment of gout, which is a disease caused by excess uric acid, forming crystals in joints.
- The Medical Biochemistry Page
- Purine metabolism - Reference pathway
- PUMPA: Purine Metabolic Patients’ Association