Biological Chemistry · 2005 · 13 citations · 29 references
Life SciencesBiochemistryMolecular BiologyEnzyme MechanismEnzymologyProtein BiochemistryEnzyme InhibitionEnzyme-substrate RecognitionPeptide ChemistryProtein StructureProteolytic EnzymesProteolytic ProcessingActivationCathepsin ActivityCysteine Protease MechanismCysteine ProteasesPropeptide ProcessingProtease Catalytic MechanismsProtease Cleavage SpecificityProtease Selectivity
Free propeptides are known to function as inhibitors of the parental mature cysteine cathepsins. This general rule, however, does not apply to the aminopeptidase cathepsin H. Screening of propeptide fragments for their inhibitory potency revealed no significant effect on the native mature cathepsin H. On the other hand, inhibitory interaction was established with recombinant cathepsin H that displays endopeptidase activity due to a lack of the mini-chain. This finding suggests that the propeptide-binding region is structurally rearranged during maturation processing and mini-chain formation, which impairs the effective recognition of mature cathepsin H by its own propeptide.
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The determination of enzyme inhibitor constants
Martin Dixon · Biochemical Journal · 1953 · 4.1K citations · Full text
Tina Cirman, Kristina Orešić, Gabriela Droga Mazovec et al. · Journal of Biological Chemistry · 2004 · 470 citations · Full text