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6-phosphogluconate dehydrogenase
From Proteopedia
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| + | <StructureSection load='1pgo' size='340' side='right' caption='6-phosphogluconate dehydrogenase dimer complex with cofactor NADP (PDB code [[1pgo]])' scene=''> | ||
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Please use the "3D" button above this box to insert a Jmol applet (molecule) on this page. | Please use the "3D" button above this box to insert a Jmol applet (molecule) on this page. | ||
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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. | 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. | ||
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| + | </StructureSection> | ||
==3D structures of 6-phosphogluconate dehydrogenase== | ==3D structures of 6-phosphogluconate dehydrogenase== | ||
Revision as of 10:41, 26 October 2015
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3D structures of 6-phosphogluconate dehydrogenase
Updated on 26-October-2015
