3hff: Difference between revisions
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Revision as of 17:02, 24 June 2009
Monomeric human Cu,Zn Superoxide dismutase without Zn ligands
Template:ABSTRACT PUBMED 19497878
Disease
Known disease associated with this structure: Amyotrophic lateral sclerosis, due to SOD1 deficiency OMIM:[147450]
About this Structure
3HFF is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Nordlund A, Leinartaite L, Saraboji K, Aisenbrey C, Grobner G, Zetterstrom P, Danielsson J, Logan DT, Oliveberg M. Functional features cause misfolding of the ALS-provoking enzyme SOD1. Proc Natl Acad Sci U S A. 2009 Jun 2. PMID:19497878
Page seeded by OCA on Wed Jun 24 20:07:24 2009
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Superoxide dismutase
- Leinartait, L.
- Logan, D T.
- Nordlund, A.
- Oliveberg, M.
- Saraboji, K.
- Acetylation
- Amyotrophic lateral sclerosis
- Antioxidant
- Copper
- Cytoplasm
- Disease mutation
- Disulfide bond
- Metal-binding
- Monomeric mutant
- Neurodegeneration
- Oxidoreductase
- Phosphoprotein
- Sod1
- Ubl conjugation
- Zinc
