6-phosphogluconate dehydrogenase

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 10: Line 10:
6PGD deficiency is an autosomal hereditary disease which manifests itself by abnormal breakdown of red blood cells. Treatment involves avoidance of drugs or foods which can cause hemolysis.<ref>PMID:18159462</ref>
6PGD deficiency is an autosomal hereditary disease which manifests itself by abnormal breakdown of red blood cells. Treatment involves avoidance of drugs or foods which can cause hemolysis.<ref>PMID:18159462</ref>
 +
 +
==3D structures of 6-phosphogluconate dehydrogenase==
 +
[[6-phosphogluconate dehydrogenase 3D structures]]
</StructureSection>
</StructureSection>
Line 35: Line 38:
**[[2jkv]] - h6PGD + NADP <BR />
**[[2jkv]] - h6PGD + NADP <BR />
**[[4gwk]] - h6PGD + 3PG<br />
**[[4gwk]] - h6PGD + 3PG<br />
 +
**[[5uq9]] - h6PDH + dioxolan derivative<br />
 +
**[[6fqz]] - Pf6PDH + 6PG – ''Plasmodium falciparum''<br />
 +
**[[6fqy]] - Pf6PDH + NADP <br />
**[[2zya]] - Ec6PGD (mutant) + 6PG – ''Escherichia coli''<BR />
**[[2zya]] - Ec6PGD (mutant) + 6PG – ''Escherichia coli''<BR />
**[[2w8z]], [[2w90]] - 6PGD + 6PG – ''Geobacillus stearothermophilus''<BR />
**[[2w8z]], [[2w90]] - 6PGD + 6PG – ''Geobacillus stearothermophilus''<BR />
Line 49: Line 55:
**[[3w6z]] – Pc6PGD (mutant) + NADP + monophosphoadenosine diphosphoribose <br />
**[[3w6z]] – Pc6PGD (mutant) + NADP + monophosphoadenosine diphosphoribose <br />
**[[5u5g]] - 6PDH + NADP + 2-oxopropyl phosphonate – ''Pseudomonas syringae''<br />
**[[5u5g]] - 6PDH + NADP + 2-oxopropyl phosphonate – ''Pseudomonas syringae''<br />
 +
**[[6fqx]] - Pf6PDH + NADP + 6PG <br />
*6PGD quaternary complex
*6PGD quaternary complex

Revision as of 09:26, 21 February 2019

Sheep 6-phosphogluconate dehydrogenase complex with cofactor NADP and sulfate (PDB code 1pgo)

Drag the structure with the mouse to rotate

3D structures of 6-phosphogluconate dehydrogenase

Updated on 21-February-2019

References

  1. Beam TR Jr. Quinolone therapy in intensive care unit settings. New Horiz. 1993 May;1(2):187-93. PMID:7922402
  2. Monga A, Makkar RP, Arora A, Mukhopadhyay S, Gupta AK. Case report: Acute hepatitis E infection with coexistent glucose-6-phosphate dehydrogenase deficiency. Can J Infect Dis. 2003 Jul;14(4):230-1. PMID:18159462

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman

Personal tools