3gw0
From Proteopedia
UROD mutant G318R
Disease
Known disease associated with this structure: Porphyria cutanea tarda OMIM:[176100], Porphyria, hepatoerythropoietic OMIM:[176100]
About this Structure
3GW0 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Wed Jul 8 12:42:28 2009
Categories: Homo sapiens | Uroporphyrinogen decarboxylase | Hill, C P. | Kushner, J P. | Phillips, J D. | Warby, C. | Whitby, F G. | Acetylation | Cytoplasm | Decarboxylase | Disease mutation | Heme biosynthesis | Heme biosynthesis. porphyria | Lyase | Phosphoprotein | Porphyrin biosynthesis | Uroporphyrinogen
