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Glucose 6-phosphate !

Glucose 6-phosphate is glucose trapped in the cell: from here it can go to energy, to glycogen or to the pentose pathway.

Updated 2026-10-31

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Key facts

  • It is made in the first step of glycolysis (hexokinase or glucokinase), using one ATP.
  • It is a crossroads: glycolysis, glycogen synthesis (via glucose 1-phosphate) and the pentose phosphate pathway (G6PD).
  • Only the liver and kidney have glucose-6-phosphatase, which turns it back into free glucose for the blood.
Also called
G6P
Formula
C₆H₁₃O₉P
PubChem
CID 439427

Structure

  • The phosphate sits on carbon 6, the CH₂OH outside the ring; at cell pH it carries two negative charges.

Clinical notes

  • Lack of glucose-6-phosphatase (von Gierke disease, glycogen storage disease Ia) causes severe fasting hypoglycemia, a large liver and lactic acidosis.
  • G6PD uses G6P to make NADPH, which shields red cells from oxidative damage; its deficiency is common in Latin America.

Pathways

Test yourself

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

Which organs can release free glucose from glucose 6-phosphate?

The liver and the renal cortex, because they have glucose-6-phosphatase.

Which enzyme starts the pentose phosphate pathway from G6P?

Glucose-6-phosphate dehydrogenase (G6PD), which makes NADPH.

What disease does lack of glucose-6-phosphatase cause?

Glycogen storage disease type Ia (von Gierke): fasting hypoglycemia, a large liver, lactic acidosis.

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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: beta-D-Glucose 6-phosphate (CID 439427) (PubChem, NCBI, 2026) · Public domain; Glucose-6-phosphate dehydrogenase deficiency: MedlinePlus Genetics (MedlinePlus, US National Library of Medicine, 2026); Textbook of Biochemistry for Medical Students, 6th ed. (Jaypee Brothers Medical Publishers (Vasudevan DM, Sreekumari S, Vaidyanathan K), 2011).

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