AbstractIn this paper the universal validity of the substrate mimetic concept in enzymatic C-N ligations was expanded to anionic leaving groups based on the specificity determinants of Glu-specific endopeptidase from Staphylococcus aureus (V8 protease). In an empirical way a specific mimetic moiety was designed from simple structure-function relationship studies. The general function of the newly developed substrate mimetics to serve as an artificial recognition site for V8 protease have been examined by hydrolysis kinetic studies. Enzymatic peptide syntheses qualify the strategy of substrate mimetics as a powerful concept for programming the enzyme specificity in the direction of a more universal application of enzymes in the general area ...
Proteins have desirable functionality in applications other than that of their biological origin, su...
Enzymes are large biomolecules which catalyze complex reactions with high selectivity and ...
Harnessing the modular architecture of non-ribosomal peptide synthetases for combinatorial biosynthe...
This article reports on the design and characteristics of substrate mimetics in protease-catalyzed r...
A family of engineered endopeptidases has been created that is capable of cleaving a diverse array o...
The exquisite selectivity and catalytic activity of enzymes have been shaped by the effects of posit...
Contains fulltext : 103347.pdf (publisher's version ) (Closed access)Enzyme-specif...
ABSTRACT: Histidine 57 of the catalytic triad of trypsin was replaced with alanine to determine whet...
The preparation of artificial proteins capable of catalyzing (non-)biological reactions with an effi...
The cost of chemical synthesis of pharmaceuticals contributes significantly to their final price and...
AbstractBackground: Peptide-ligating technologies facilitate a range of manipulations for the study ...
AbstractWe present a model for the three-dimensional structure of the glutamate-specific endopeptida...
Proteolytic enzymes (proteases) comprise a group of hydrolases (EC 3.4, NC-IUBMB) which share the co...
Proteases, enzymes that catalyze the hydrolysis of amide bonds in peptides and proteins, are ubiquit...
Content removed due to copyright restrictions: Lenz, D. H., Norris, G. E., Taylor, C. M., & Slim, G...
Proteins have desirable functionality in applications other than that of their biological origin, su...
Enzymes are large biomolecules which catalyze complex reactions with high selectivity and ...
Harnessing the modular architecture of non-ribosomal peptide synthetases for combinatorial biosynthe...
This article reports on the design and characteristics of substrate mimetics in protease-catalyzed r...
A family of engineered endopeptidases has been created that is capable of cleaving a diverse array o...
The exquisite selectivity and catalytic activity of enzymes have been shaped by the effects of posit...
Contains fulltext : 103347.pdf (publisher's version ) (Closed access)Enzyme-specif...
ABSTRACT: Histidine 57 of the catalytic triad of trypsin was replaced with alanine to determine whet...
The preparation of artificial proteins capable of catalyzing (non-)biological reactions with an effi...
The cost of chemical synthesis of pharmaceuticals contributes significantly to their final price and...
AbstractBackground: Peptide-ligating technologies facilitate a range of manipulations for the study ...
AbstractWe present a model for the three-dimensional structure of the glutamate-specific endopeptida...
Proteolytic enzymes (proteases) comprise a group of hydrolases (EC 3.4, NC-IUBMB) which share the co...
Proteases, enzymes that catalyze the hydrolysis of amide bonds in peptides and proteins, are ubiquit...
Content removed due to copyright restrictions: Lenz, D. H., Norris, G. E., Taylor, C. M., & Slim, G...
Proteins have desirable functionality in applications other than that of their biological origin, su...
Enzymes are large biomolecules which catalyze complex reactions with high selectivity and ...
Harnessing the modular architecture of non-ribosomal peptide synthetases for combinatorial biosynthe...