摘要: Work with new, quenched fluorescence substrates of Pz-peptidase has led to the discovery that Pz-peptidase, soluble metallo-endopeptidase and endo-oligopeptidase A are either identical, or very closely related enzymes. is a marked thiol-dependence. It been confirmed inhibitors type designed by Orlowski for effective tools in studying Pz-peptidase. There little evidence support proposed role connective tissue matrix degradation, main function enzyme may be intracellular.
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