EC Number |
Title |
Organism |
---|
3.4.24.84 | Human CaaX protease ZMPSTE24 expressed in yeast Structure and inhibition by HIV protease inhibitors |
Homo sapiens |
3.4.24.84 | Ste24p mediates proteolysis of both isoprenylated and non-prenylated oligopeptides |
Saccharomyces mikatae |
3.4.24.84 | ZMPSTE24 missense mutations that cause progeroid diseases decrease prelamin A cleavage activity and/or protein stability |
Homo sapiens |
3.4.24.84 | A novel membrane-associated metalloprotease, Ste24p, is required for the first step of NH2-terminal processing of the yeast a-factor precursor |
Saccharomyces cerevisiae |
3.4.24.84 | Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation |
Mus musculus |
3.4.24.84 | Accelerated features of age-related bone loss in zmpste24 metalloproteinase-deficient mice |
Mus musculus |
3.4.24.84 | Biochemical studies of Zmpste24-deficient mice |
Mus musculus |
3.4.24.84 | Dual roles for Ste24p in yeast a-factor maturation: NH2-terminal proteolysis and COOH-terminal CAAX processing |
Saccharomyces cerevisiae |
3.4.24.84 | Dual roles for Ste24p in yeast a-factor maturation: NH2-terminal proteolysis and COOH-terminal CAAX processing |
Homo sapiens |
3.4.24.84 | Endoplasmic reticulum membrane localization of Rce1p and Ste24p, yeast proteases involved in carboxyl-terminal CAAX protein processing and amino-terminal a-factor cleavage |
Saccharomyces cerevisiae |