Phosphoribosyl pyrophosphate

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Phosphoribosyl pyrophosphate
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MeSH Phosphoribosyl+pyrophosphate
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Template:Longitem C5H13O14P3
Molar mass 390.07 g/mol

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Phosphoribosyl pyrophosphate (PRPP) is a pentose phosphate. It is a biochemical intermediate in the formation of purine nucleotides via inosine-5-monophosphate, as well as in pyrimidine nucleotide formation. Hence it is a building block for DNA and RNA.[1][2][3] The vitamins thiamine[4] and cobalamin,[5] and the amino acid tryptophan also contain fragments derived from PRPP.[6] It is formed from ribose 5-phosphate (R5P) by the enzyme ribose-phosphate diphosphokinase:[7]

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It plays a role in transferring phospho-ribose groups in several reactions, some of which are salvage pathways:[8]

Enzyme Reactant Product
adenine phosphoribosyltransferase adenine AMP[9]
hypoxanthine-guanine phosphoribosyltransferase guanine GMP[10]
hypoxanthine-guanine phosphoribosyltransferase hypoxanthine IMP[10]
nicotinate phosphoribosyltransferase nicotinate nicotinate riboside[11]
orotate phosphoribosyltransferase orotate OMP[12]
uracil phosphoribosyltransferase uracil UMP[13]
xanthine phosphoribosyltransferase xanthine XMP[14]

In de novo generation of purines, the enzyme amidophosphoribosyltransferase acts upon PRPP to create phosphoribosylamine.[2] The histidine biosynthesis pathway involves the reaction between PRPP and ATP, which activates the latter to ring cleavage. Carbon atoms from ribose in PRPP form the linear chain and part of the imidazole ring in histidine.[15][16][17] The same is true for the biosynthesis of tryptophan, with the first step being N-alkylation of anthranilic acid catalysed by the enzyme anthranilate phosphoribosyltransferase.[15][18][19]

Increased PRPP

Increased levels of PRPP are characterized by the overproduction and accumulation of uric acid leading to hyperuricemia and hyperuricosuria. It is one of the causes of gout.[20]

Increased levels of PRPP are present in Lesch–Nyhan Syndrome. Decreased levels of hypoxanthine guanine phosphoribosyl transferase (HGPRT) causes this accumulation, as PRPP is a substrate used by HGPRT during purine salvage.[21]

See also

References

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