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Results 1 - 10 of 23 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + O2 N6,N6, N6-trimethyl-L-lysine is epsilon-N-trimethyl-L-lysine Bos taurus 3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8more determination of the (2S,3S)-3-hydroxy-N6,N6,N6-trimethyl-L-lysine and N6,N6,N6-trimethyl-L-lysine is performed by ultraperformance liquid chromatography–tandem mass spectrometry (UPLC/MS/MS) in positive ion electrospray mode Homo sapiens ? - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8more NMR spectrosopic structure analysis of substrates and products Homo sapiens ? - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8more NMR spectrosopic structure analysis of substrates and products, substrate specificity, overview. No or poor activity with dimethyllysine, methyllysine, lysine, D-trimethyllysine, 5-trimethylamino-1-aminopentane, trimethyllysine, 6-trimethylaminohexanoic acid, hexamethyllysine, N-acetyltrimethyllysine, trimethyldiaminobutyric acid, triethyllysine, symmetric and asymmetric dimethylarginines, mildronate, and gamma-butyrobetaine, structure-activity relationship study Homo sapiens ? - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N5,N5,N5-trimethyl-L-ornithine + 2-oxoglutarate + O2 - Homo sapiens (3S)-3-hydroxy-N5,N5,N5-trimethyl-L-ornithine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + O2 - Homo sapiens 3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + O2 - Homo sapiens (3S)-3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + O2 the enzymatic hydroxylation occurs at the C-3 site of (2S)-Nepsilon-trimethyllysine substrate. Comparative NMR spectroscopic studies (with two enantiopure synthetic standards that possess 3R and 3S stereochemistry) on the enzymatically produced (2S)-3-hydroxy-Nepsilon-trimethyllysine reveal that TMLH exclusively catalyzes the formation of (3S)-3-hydroxy-Nepsilon-trimethyl-L-lysine, not forming any (3R)-3-hydroxy-Nepsilon-trimethyl-L-lysine diastereoisomer Homo sapiens (3S)-3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + O2 recognition sites that contribute to the enzymatic activity of the enzyme (TMLH): the Fe(II)-binding H242-D244-H389 residues, R391-R398 involved in 2-oxoglutarate-binding, and several residues (D231, N334, and the aromatic cage comprised of W221, Y217 and Y234) associated with binding of (2S)-Nepsilon-trimethyllysine Homo sapiens (3S)-3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2 - ?
Show all pathways known for 1.14.11.8Display the word mapDisplay the reaction diagram Show all sequences 1.14.11.8N6,N6-dimethyl-N6-ethyl-L-lysine + 2-oxoglutarate + O2 - Homo sapiens (3S)-3-hydroxy-N6,N6-dimethyl-N6-ethyl-L-lysine + succinate + CO2 - ?
Results 1 - 10 of 23 > >>