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Results 1 - 10 of 16 > >>
EC Number Application Commentary Reference
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14analysis enzyme widely used as reagent to resolve amino acid racemates 288864
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14diagnostics the enzyme is an important biomarker with potential prognostic utility in patients with delayed graft function following renal transplantation. The possibility of using 4-[(E)-2-[7-(diethylamino)-2-oxo-2H-1-benzopyran-3-yl]ethenyl]phenyl prop-2-enoate for quantification of aminoacylase-1 in blood serum samples is explored. Nontoxic nature and cell membrane permeability are key features of this probe and are ideally suited for imaging intracellular Cys in normal and cancerous cell lines .CA can be used for selective detection of Cys in the presence of the competing biothiols, cations, and anions of biological relevance. This reagent is successfully utilized for monitoring the hydrolysis of an important commercial drug molecule N-acetyl-L-cysteine by an industrially and biologically important endogenous enzyme, aminoacylase-1 752480
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14medicine N-acetyl-L-cysteine used for drugs against lung disorders and HIV infections, test of potential antitumor agents 288871
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14medicine preparation of commercially important amino acids as components for semisynthetic penicillins and cephalosporins 288858
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14medicine the enzyme is an important biomarker with potential prognostic utility in patients with delayed graft function following renal transplantation 752480
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14synthesis - -, 288863, 288866, 288867, 288872, 288873
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14synthesis aminoacylase-catalyzed enantioselective synthesis of aromatic beta-amino acids 670454
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14synthesis because of its thermostability, the enzyme is expected to be useful for the production of L-amino acid derivatives from racemates at temperatures over 90°C -, 721329
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14synthesis biocatalytic production of optically active amino acids and their derivatives, which are broadly used as physiologically active compounds, chiral auxiliaries or synthons and as intermediates in pharmaceutical, food and agrochemistry 670918
Show all pathways known for 3.5.1.14Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.14synthesis enzyme used for production of L-amino acids 288863
Results 1 - 10 of 16 > >>