This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
3h2q
From Proteopedia
Human SOD1 H80R variant, P21 crystal form
Disease
Known disease associated with this structure: Amyotrophic lateral sclerosis, due to SOD1 deficiency OMIM:[147450]
About this Structure
3H2Q is a 4 chains structure with sequences from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Wed May 5 12:05:35 2010
Categories: Homo sapiens | Superoxide dismutase | Cao, X. | Carroll, M C. | Culotta, V C. | Doucette, P A. | Hart, P J. | Seetharaman, S V. | Taylor, A B. | Valentine, J S. | Whitson, L J. | Winkler, D D. | Acetylation | Amyotrophic lateral sclerosis | Antioxidant | Copper | Cytoplasm | Disease mutation | Disulfide bond | Human cu | Metal-binding | Oxidoreductase | Phosphoprotein | Ubl conjugation | Zinc | Zn superoxide dismutase
