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4fpa
From Proteopedia
Crystal Structure of recombinant human Hexokinase type I mutant D413N Glucose 6-Phosphate
Disease
[HXK1_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.
About this Structure
4fpa is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
