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Results 1 - 3 of 3
EC Number General Information Commentary Reference
Show all pathways known for 3.1.2.12Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.12metabolism FrmB activates the prodrug bis(pivaloyloxymethyl) (1-hydroxy-2-oxopiperidin-3-yl)phosphonate. Mutation of FrmB renders Staphylococcus aureus sensitive to bis(pivaloyloxymethyl) (1-hydroxy-2-oxopiperidin-3-yl)phosphonate -, 760979
Show all pathways known for 3.1.2.12Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.12physiological function FrmB has the highest activity toward oxygen ethers. FrmB hydrolyzes unbranched substrates with little regard for chain length or the end-of-chain bulk within the tested substrates. Branching at the position following the ester carbonyl is deleterious to FrmB activity. When oxygen is included in the chain, positioning at the beta-position to the carbonyl is strongly preferred over the gamma-position -, 760979
Show all pathways known for 3.1.2.12Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.12physiological function overexpression of ESD significantly suppresses foot-and-mouth disease virus FMDV replication. Knockdown of ESD expression enhances virus replication. Sendai-virus-induced interferon signaling is enhanced by upregulation of ESD. ESD protein enhances IRF3 phosphorylation during FMDV infection. Overexpression of ESD also promotes the expression of various antiviral interferon-stimulated genes, and knockdown of ESD impairs the expression of these antiviral genes during FMDV infection 751579
Results 1 - 3 of 3