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
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. See AlsoContents | ||||||||||||||||||||||
This page was last modified 21:47, 25 December 2014.