amidase การใช้

• This is due to the activity of domesticated amidase effector ( dae ) genes.
• A study testing possible interactions with amidase inhibitors is part of the post-authorisation development plan.
• Ply118 is a 30.8kDa L-alanoyl-D-glutamate peptidase and Ply511 ( 36.5 kDa ) acts as N-acetylmuramoyl-L-alanine amidase ( INTERPRO ).
• An additional domain is found at the N-terminal of some copper amine oxidases, as well as in related proteins such as cell wall hydrolase and N-acetylmuramoyl-L-alanine amidase.
• It produces penicillin amidase used to make synthetic penicillin, various amylases used in the baking industry and antiviral properties, etc . It produces enzymes for modifying corticosteroids, as well as several amino acid dehydrogenases.
• Evidence for this regulation is that the residues which allow the synthase domain to block the amidase active site are highly conserved among different species of kinetoplastids, indicating that they are key in the enzyme's function and that the binding of certain substrates might cause conformational shifts that would open up the amidase active site.
• Evidence for this regulation is that the residues which allow the synthase domain to block the amidase active site are highly conserved among different species of kinetoplastids, indicating that they are key in the enzyme's function and that the binding of certain substrates might cause conformational shifts that would open up the amidase active site.
• FAAH is an integral membrane hydrolase with a single " N "-terminal transmembrane domain . " In vitro ", FAAH has esterase and amidase activity . " In vivo ", FAAH is the principal catabolic enzyme for a class of bioactive lipids called the fatty acid amides ( FAAs ).
• The mechanisms of toxicity toward target cells exhibited by T6SS substrates are diverse, but tend to involve targeting of highly conserved bacterial structures, including degradation of the cell wall through amidase or glycohydrolase activity, disruption of cell membranes through lipase activity or pore formation, cleavage of DNA, and degradation of the essential metabolite NAD +.
• Collaborating with Italian chemists, Giorgio Tarzia ( University of Urbino  Carlo Bo ) and Marco Mor ( University of Parma ), he developed the first systemically active inhibitors of the degradation of anandamide ( Fatty Acid Amide Hydrolase inhibitors ), PEA ( N-Acylethanolamide Acid Amidase inhibitors ), and ceramide ( Acid Ceramidase inhibitors ).
• Endo-?-N-acetylglucosaminidase lysins cleave NAGs while N-acetylmuramidase lysins ( lysozyme-like lysins ) cleave NAMs . Endopeptidase lysins cleave any of the peptide bonds between amino acids, whereas N-acetylmuramoyl-l-alanine amidase lysins ( or simply amidase lysins ) hydrolyze the amide bond between the sugar and the amino acid moieties.
• Endo-?-N-acetylglucosaminidase lysins cleave NAGs while N-acetylmuramidase lysins ( lysozyme-like lysins ) cleave NAMs . Endopeptidase lysins cleave any of the peptide bonds between amino acids, whereas N-acetylmuramoyl-l-alanine amidase lysins ( or simply amidase lysins ) hydrolyze the amide bond between the sugar and the amino acid moieties.