3gqf
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Revision as of 09:31, 9 April 2009
Structural and Biophysical Properties of the Pathogenic SOD1 Variant H46R/H48Q
Disease
Known disease associated with this structure: Amyotrophic lateral sclerosis, due to SOD1 deficiency OMIM:[147450]
About this Structure
3GQF is a 6 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Apr 9 12:31:34 2009
Categories: Homo sapiens | Superoxide dismutase | Hart, P J. | Schuermann, J P. | Winkler, D D. | Acetylation | Amyotrophic lateral sclerosis | Antioxidant | Copper | Cytoplasm | Disease mutation | Disulfide bond | Familial amyotrophic lateral sclerosis mutant | Human cu-zn superoxide dismutase | Metal-binding | Oxidoreductase | Phosphoprotein | Superoxide acceptor | Ubl conjugation | Zinc
