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Crystal Structure of recombinant human Hexokinase type I mutant D413N with Glucose 1,6-bisphosphateCrystal Structure of recombinant human Hexokinase type I mutant D413N with Glucose 1,6-bisphosphate
Structural highlights
DiseaseHXK1_HUMAN Defects in HK1 are the cause of hexokinase deficiency (HK deficiency) [MIM:235700. HK deficiency is a rare autosomal recessive disease with nonspherocytic hemolytic anemia as the predominant clinical feature. FunctionSee Also |
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