Glucose-6-phosphate dehydrogenase

Glucose-6-phosphate dehydrogenase, NAD binding domain
glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroides
Identifiers
SymbolG6PD_N
PfamPF00479
Pfam clanCL0063
InterProIPR022674
PROSITEPDOC00067
SCOP21dpg / SCOPe / SUPFAM
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Glucose-6-phosphate dehydrogenase
Identifiers
EC no.1.1.1.49
CAS no.9001-40-5
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins

Glucose-6-phosphate dehydrogenase (G6PD or G6PDH) (EC 1.1.1.49) is a cytosolic enzyme that catalyzes the chemical reaction

D-glucose 6-phosphate + NADP+ + H2O6-phospho-D-glucono-1,5-lactone + NADPH + H+

This enzyme participates in the pentose phosphate pathway (see image), a metabolic pathway that supplies reducing energy to cells (such as erythrocytes) by maintaining the level of the reduced form of the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH). The NADPH in turn maintains the level of glutathione in these cells that helps protect the red blood cells against oxidative damage from compounds like hydrogen peroxide.[1] Of greater quantitative importance is the production of NADPH for tissues involved in biosynthesis of fatty acids or isoprenoids, such as the liver, mammary glands, adipose tissue, and the adrenal glands. G6PD reduces NADP+ to NADPH while oxidizing glucose-6-phosphate.[2] Glucose-6-phosphate dehydrogenase is also an enzyme in the Entner–Doudoroff pathway, a type of glycolysis.

Clinically, an X-linked genetic deficiency of G6PD makes a human prone to non-immune hemolytic anemia.[3]

  1. ^ Thomas D, Cherest H, Surdin-Kerjan Y (March 1991). "Identification of the structural gene for glucose-6-phosphate dehydrogenase in yeast. Inactivation leads to a nutritional requirement for organic sulfur". The EMBO Journal. 10 (3): 547–53. doi:10.1002/j.1460-2075.1991.tb07981.x. PMC 452682. PMID 2001672.
  2. ^ Aster J, Kumar V, Robbins SL, Abbas AK, Fausto N, Cotran RS (2010). Robbins and Cotran Pathologic Basis of Disease. Saunders/Elsevier. pp. Kindle Locations 33340–33341. ISBN 978-1-4160-3121-5.
  3. ^ Cite error: The named reference pmid18177777 was invoked but never defined (see the help page).