Ontology highlight
ABSTRACT:
SUBMITTER: Kolli N
PROVIDER: S-EPMC4002070 | biostudies-literature | 2014 Apr
REPOSITORIES: biostudies-literature
Kolli Nilima N Garman Scott C SC
The Journal of biological chemistry 20140305 17
Galactosialidosis is a human lysosomal storage disease caused by deficiency in the multifunctional lysosomal protease cathepsin A (also known as protective protein/cathepsin A, PPCA, catA, HPP, and CTSA; EC 3.4.16.5). Previous structural work on the inactive precursor human cathepsin A (zymogen) led to a two-stage model for activation, where proteolysis of a 1.6-kDa excision peptide is followed by a conformational change in a blocking peptide occluding the active site. Here we present evidence f ...[more]