3gw3 | pdb_00003gw3
From Proteopedia
human UROD mutant K297N
Disease
Known disease associated with this structure: Porphyria cutanea tarda OMIM:[176100], Porphyria, hepatoerythropoietic OMIM:[176100]
About this Structure
3GW3 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 12:42:35 2009