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PRPP (phosphoribosyl pyrophosphate) !

PRPP is activated ribose: the starting point for making and recycling every nucleotide.

Updated 2026-11-01

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Key facts

  • It is made from ribose-5-phosphate and ATP by PRPP synthetase.
  • It is used by de novo purine synthesis (committed step), pyrimidine synthesis (UMP synthase), base salvage (HGPRT, APRT) and NAD⁺ synthesis.
  • Its concentration controls purine synthesis: more PRPP, more amidotransferase activity.
  • It rises in HGPRT deficiency and in PRPP synthetase superactivity: both cause hyperuricaemia.
Also called
5-Phosphoribosyl-1-pyrophosphate
Formula
C₅H₁₃O₁₄P₃
PubChem
CID 7339

Structure

  • A ribofuranose ring with a phosphate on C5 and an α-pyrophosphate on C1.
  • When a base attaches, the pyrophosphate leaves and the bond ends up β, as in nucleotides.

Clinical notes

  • In Lesch-Nyhan syndrome PRPP unused by HGPRT accumulates in red cells and speeds purine synthesis.
  • Hydrolysis of the released pyrophosphate makes PRPP-using reactions irreversible.

Pathways

Test yourself

Think of the answer, then tap the question to see it.

Which enzyme makes PRPP, and from what?

PRPP synthetase, from ribose-5-phosphate and ATP (which is left as AMP).

Why does PRPP rise in HGPRT deficiency?

HGPRT is a major PRPP consumer; without it PRPP is left over and stimulates de novo purine synthesis.

How does PRPP use differ between purines and pyrimidines?

In purines the ring is built on PRPP; in pyrimidines the finished ring (orotate) is attached to PRPP.

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Molecules are shown in their neutral form, as the databases deposit them; in the cell the acids and phosphates are ionised.

Educational information, not medical advice. For any symptom, see a health professional.

Sources: Phosphoribosyl Pyrophosphate (CID 7339) (PubChem, NCBI, 2026) · Public domain; Purine ribonucleoside monophosphate biosynthesis (Reactome, 2026); Textbook of Biochemistry for Medical Students, 6th ed. (Jaypee Brothers Medical Publishers (Vasudevan DM, Sreekumari S, Vaidyanathan K), 2011).

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