6-Phosphogluconate dehydrogenase

Class of enzymes From Wikipedia, the free encyclopedia

6-Phosphogluconate dehydrogenase (6PGD) is an enzyme in the pentose phosphate pathway. It forms ribulose 5-phosphate from 6-phosphogluconate:[2]

 
 
 
H+
Reversible left-right reaction arrow with minor forward product(s) to top right and minor reverse substrate(s) from bottom right
 
H+
 
+ CO2 + NADH
 

Quick facts 6PGD, Identifiers ...
6PGD
Crystallographic structure of sheep 6-phosphogluconate dehydrogenase complexed with adenosine 2'-monophosphate[1]
Identifiers
Symbol6PGD
PfamPF00393
Pfam clanCL0106
InterProIPR006114
PROSITEPDOC00390
SCOP22pgd / SCOPe / SUPFAM
Available protein structures:
PDB  IPR006114 PF00393 (ECOD; PDBsum)  
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Quick facts Phosphogluconate dehydrogenase, Identifiers ...
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Quick facts phosphogluconate dehydrogenase, Identifiers ...
phosphogluconate dehydrogenase
Identifiers
SymbolPGD
NCBI gene5226
HGNC8891
OMIM172200
RefSeqNM_002631
UniProtP52209
Other data
EC number1.1.1.44
LocusChr. 1 p36.3-36.13
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StructuresSwiss-model
DomainsInterPro
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It is an oxidative carboxylase that catalyses the oxidative decarboxylation of 6-phosphogluconic acid into ribulose 5-phosphate in the presence of oxidised NAD+. This reaction is a component of the hexose mono-phosphate shunt and pentose phosphate pathways (PPP).[3][4] Prokaryotic and eukaryotic 6PGD are proteins of about 470 amino acids whose sequences are highly conserved.[5] The protein is a homodimer in which the monomers act independently:[4] each contains a large, mainly alpha-helical domain and a smaller beta-alpha-beta domain, containing a mixed parallel and anti-parallel 6-stranded beta sheet.[4] NADP is bound in a cleft in the small domain, the substrate binding in an adjacent pocket.[4]

Biotechnological significance

Recently, 6PGD was demonstrated to catalyze also the reverse reaction (i.e. reductive carboxylation) in vivo.[6] Experiments using Escherichia coli selection strains revealed that this reaction was efficient enough to support the formation of biomass based solely on CO2 and pentose sugars. In the future, this property could be exploited for synthetic carbon fixation routes.

Clinical significance

Mutations within the gene coding this enzyme result in 6-phosphogluconate dehydrogenase deficiency, an autosomal hereditary disease affecting the red blood cells.

As a possible drug target

6PGD is involved in cancer cell metabolism so 6PGD inhibitors have been sought.[7]

See also

References

Further reading

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