9ey8 | pdb_00009ey8
From Proteopedia
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Structural highlights
DiseaseTYRP1_HUMAN Oculocutaneous albinism type 3. The disease is caused by mutations affecting the gene represented in this entry. FunctionTYRP1_HUMAN Catalyzes the oxidation of 5,6-dihydroxyindole-2-carboxylic acid (DHICA) into indole-5,6-quinone-2-carboxylic acid. May regulate or influence the type of melanin synthesized. Also to a lower extent, capable of hydroxylating tyrosine and producing melanin.[UniProtKB:P07147] Contents | ||||||||||||||||||||
This page was last modified 06:26, 1 May 2024.