Mutations in Calpain 3 Associated with Limb Girdle Muscular Dystrophy: Analysis by Molecular Modeling and by Mutation in m-Calpain
Open Access
- 1 June 2001
- journal article
- Published by Elsevier in Biophysical Journal
- Vol. 80 (6) , 2590-2596
- https://doi.org/10.1016/s0006-3495(01)76229-7
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Roles of individual EF-hands in the activation of m-calpain by calciumBiochemical Journal, 2000
- Crystal structure of calpain reveals the structural basis for Ca2+-dependent protease activity and a novel mode of enzyme activationThe EMBO Journal, 1999
- Calpainopathy—A Survey of Mutations and PolymorphismsAmerican Journal of Human Genetics, 1999
- Calpain: A Protease in Search of a Function?Biochemical and Biophysical Research Communications, 1998
- Juvenile limb-girdle muscular dystrophyBrain, 1996
- Recombinant calpain II: improved expression systems and production of a C105A active-site mutant for crystallographyProtein Engineering, Design and Selection, 1995
- Active site residues in m‐calpain: identification by site‐directed mutagenesisFEBS Letters, 1995
- Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2ACell, 1995
- PROCHECK: a program to check the stereochemical quality of protein structuresJournal of Applied Crystallography, 1993
- MOLSCRIPT: a program to produce both detailed and schematic plots of protein structuresJournal of Applied Crystallography, 1991