1QKI
X-RAY STRUCTURE OF HUMAN GLUCOSE 6-PHOSPHATE DEHYDROGENASE (VARIANT CANTON R459L) COMPLEXED WITH STRUCTURAL NADP+
Summary for 1QKI
| Entry DOI | 10.2210/pdb1qki/pdb |
| Related | 1DPG 2DPG |
| Descriptor | GLUCOSE-6-PHOSPHATE 1-DEHYDROGENASE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, GLYCOLIC ACID, ... (5 entities in total) |
| Functional Keywords | oxidoreductase, oxidoredutase, (choh(d)-nadp), glucose metabolism |
| Biological source | HOMO SAPIENS (HUMAN) |
| Total number of polymer chains | 8 |
| Total formula weight | 480355.05 |
| Authors | Au, S.W.N.,Gover, S.,Lam, V.M.S.,Adams, M.J. (deposition date: 1999-07-20, release date: 2000-03-16, Last modification date: 2023-12-13) |
| Primary citation | Au, S.W.N.,Gover, S.,Lam, V.M.S.,Adams, M.J. Human Glucose-6-Phosphate Dehydrogenase: The Crystal Structure Reveals a Structural Nadp+ Molecule and Provides Insights Into Enzyme Deficiency Structure, 8:293-, 2000 Cited by PubMed Abstract: Glucose-6-phosphate dehydrogenase (G6PD) catalyses the first committed step in the pentose phosphate pathway; the generation of NADPH by this enzyme is essential for protection against oxidative stress. The human enzyme is in a dimer<-->tetramer equilibrium and its stability is dependent on NADP(+) concentration. G6PD deficiency results from many different point mutations in the X-linked gene encoding G6PD and is the most common human enzymopathy. Severe deficiency causes chronic non-spherocytic haemolytic anaemia; the usual symptoms are neonatal jaundice, favism and haemolytic anaemia. PubMed: 10745013DOI: 10.1016/S0969-2126(00)00104-0 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3 Å) |
Structure validation
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