4fpa | pdb_00004fpa

Crystal Structure of recombinant human Hexokinase type I mutant D413N Glucose 6-Phosphate

spinqualitylabelsall models 4fpa, resolution 2.48Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 4fpa is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: BG6, BGC, CIT, NA Related: 4foe, 4foi, 4fpb Gene: HK1 (Homo sapiens) Activity: Hexokinase, with EC number 2.7.1.1 Resources: FirstGlance, OCA, RCSB, PDBsum 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 Also Hexokinase

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