4f9o | pdb_00004f9o
From Proteopedia
Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate
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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 | ||||||||||||||||||
This page was last modified 04:43, 7 October 2022.