3s5n | pdb_00003s5n
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Crystal Structure of Human 4-hydroxy-2-oxoglutarate Aldolase
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Structural highlights
DiseaseHOGA1_HUMAN Primary hyperoxaluria type 3. The disease is caused by mutations affecting the gene represented in this entry. FunctionHOGA1_HUMAN Catalyzes the final step in the metabolic pathway of hydroxyproline.[1] [2] See AlsoReferences
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This page was last modified 09:47, 1 March 2024.