The C-terminal Region of proSAAS Is a Potent Inhibitor of Prohormone Convertase 1
Open Access
- 1 August 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (31) , 23596-23601
- https://doi.org/10.1074/jbc.m001583200
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- The Prosegments of Furin and PC7 as Potent Inhibitors of Proprotein ConvertasesPublished by Elsevier ,1999
- Proteolytic Processing in the Secretory PathwayJournal of Biological Chemistry, 1999
- Localization of Metallocarboxypeptidase D in AtT-20 CellsPublished by Elsevier ,1999
- Proprotein Convertase PC1/3-related Peptides Are Potent Slow Tight-binding Inhibitors of Murine PC1/3 and HfurinJournal of Biological Chemistry, 1998
- Eukaryotic protein processing: endoproteolysis of precursor proteinsCurrent Opinion in Biotechnology, 1997
- Internal cleavage of the inhibitory 7B2 carboxyl-terminal peptide by PC2: a potential mechanism for its inactivation.Proceedings of the National Academy of Sciences, 1996
- 7B2 is a neuroendocrine chaperone that transiently interacts with prohormone convertase PC2 in the secretory pathwayCell, 1994
- Proteolytic processing of the hepatocyte growth factor/scatter factor receptor by furinFEBS Letters, 1993
- Human fur gene encodes a yeast KEX2-like endoprotease that cleaves pro-beta-NGF in vivo.The Journal of cell biology, 1990
- Isolation and NH2‐terminal sequence of a novel porcine anterior pituitary polypeptideFEBS Letters, 1982