EC Number |
BRENDA No. |
Title |
Journal |
Volume |
Pages |
Year |
Organism |
PubMed ID |
---|
3.4.24.84 | 753395 |
ZMPSTE24 missense mutations that cause progeroid diseases decrease prelamin A cleavage activity and/or protein stability |
Dis. Model. Mech. |
11 |
dmm033670 |
2018 |
Homo sapiens |
29794150 |
3.4.24.84 | 755334 |
Human CaaX protease ZMPSTE24 expressed in yeast Structure and inhibition by HIV protease inhibitors |
Protein Sci. |
26 |
242-257 |
2017 |
Homo sapiens |
27774687 |
3.4.24.84 | 754136 |
Ste24p mediates proteolysis of both isoprenylated and non-prenylated oligopeptides |
J. Biol. Chem. |
291 |
14185-14198 |
2016 |
Saccharomyces mikatae |
27129777 |
3.4.24.84 | 682549 |
HIV protease inhibitors block the zinc metalloproteinase ZMPSTE24 and lead to an accumulation of prelamin A in cells |
Proc. Natl. Acad. Sci. USA |
104 |
13432-13437 |
2007 |
Mus musculus |
17652517 |
3.4.24.84 | 669751 |
Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy |
J. Invest. Dermatol. |
125 |
913-919 |
2005 |
Homo sapiens |
16297189 |
3.4.24.84 | 638973 |
A novel membrane-associated metalloprotease, Ste24p, is required for the first step of NH2-terminal processing of the yeast a-factor precursor |
J. Cell Biol. |
136 |
271-285 |
1997 |
Saccharomyces cerevisiae |
9015299 |
3.4.24.84 | 638974 |
Dual roles for Ste24p in yeast a-factor maturation: NH2-terminal proteolysis and COOH-terminal CAAX processing |
J. Cell Biol. |
142 |
635-649 |
1998 |
Saccharomyces cerevisiae |
9700155 |
3.4.24.84 | 638974 |
Dual roles for Ste24p in yeast a-factor maturation: NH2-terminal proteolysis and COOH-terminal CAAX processing |
J. Cell Biol. |
142 |
635-649 |
1998 |
Homo sapiens |
9700155 |
3.4.24.84 | 651423 |
Roles pf prenyl protein proteases in maturation of Saccharomyces cerevisiae |
Genetics |
150 |
95-1001 |
1998 |
Saccharomyces cerevisiae |
9725832 |
3.4.24.84 | 710803 |
Novel frameshifting mutations of the ZMPSTE24 gene in two siblings affected with restrictive dermopathy and review of the mutations described in the literature |
Am. J. Med. Genet. A |
152A |
447-452 |
2010 |
Homo sapiens |
20101687 |