1ja8
From Proteopedia
Contents |
Kinetic Analysis of Product Inhibition in Human Manganese Superoxide Dismutase
Template:ABSTRACT PUBMED 11580280
Disease
[SODM_HUMAN] Genetic variation in SOD2 is associated with susceptibility to microvascular complications of diabetes type 6 (MVCD6) [MIM:612634]. These are pathological conditions that develop in numerous tissues and organs as a consequence of diabetes mellitus. They include diabetic retinopathy, diabetic nephropathy leading to end-stage renal disease, and diabetic neuropathy. Diabetic retinopathy remains the major cause of new-onset blindness among diabetic adults. It is characterized by vascular permeability and increased tissue ischemia and angiogenesis.
Function
[SODM_HUMAN] Destroys superoxide anion radicals which are normally produced within the cells and which are toxic to biological systems.[1]
About this Structure
1ja8 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Hearn AS, Stroupe ME, Cabelli DE, Lepock JR, Tainer JA, Nick HS, Silverman DN. Kinetic analysis of product inhibition in human manganese superoxide dismutase. Biochemistry. 2001 Oct 9;40(40):12051-8. PMID:11580280
- ↑ MacMillan-Crow LA, Thompson JA. Tyrosine modifications and inactivation of active site manganese superoxide dismutase mutant (Y34F) by peroxynitrite. Arch Biochem Biophys. 1999 Jun 1;366(1):82-8. PMID:10334867 doi:S0003-9861(99)91202-X
Categories: Homo sapiens | Superoxide dismutase | Cabelli, D E. | Hearn, A S. | Lepock, J R. | Nick, H S. | Silverman, D S. | Stroupe, M E. | Tainer, J A. | Alpha-beta | Disumtase | Homo sapien | Homotetramer | Hydrogen bond network | Manganese | Mnsod | Oxidoreductase | Sod | Superoxide | Two-domain