4foe | pdb_00004foe
From Proteopedia
Crystal Structure of recombinant human Hexokinase type I with Mannose 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 20:03, 19 October 2022.