Competitive Inhibition of Cathepsin C by Guanidinium Ions and Reexamination of Substrate Inhibition
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference28 articles.
1. Oligomeric Structure and Substrate Induced Inhibition of Human Cathepsin C
2. Molecular cloning of cDNA for rat cathepsin C. Cathepsin C, a cysteine proteinase with an extremely long propeptide.
3. Purification and characterization of cathepsin J from rat liver
4. Stoichiometry and heterogeneity of the pro-region chain in tetrameric human cathepsin C
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1. Cathepsin C: structure, function, and pharmacological targeting;Rare Disease and Orphan Drugs Journal;2023-07-26
2. Trimacrocyclic hexasubstituted benzenes for recognition of guanidinium and their anti-cancer and antimicrobial activities;Organic Chemistry Frontiers;2022
3. Interplay between tetrameric structure, enzymatic activity and allosteric regulation of human dipeptidyl-peptidase I;Archives of Biochemistry and Biophysics;2019-10
4. Strategies to improve plasma half life time of peptide and protein drugs;Amino Acids;2006-04-20
5. The Residual Pro-Part of Cathepsin C Fulfills the Criteria Required for an Intramolecular Chaperone in Folding and Stabilizing the Human Proenzyme;Biochemistry;2000-09-14
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