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Results 1 - 10 of 52 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25cystathionine ketimine + NADH - Bos taurus cyclothionine + NAD+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25cystathionine ketimine + NADPH - Bos taurus cyclothionine + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA1-piperideine 2-carboxylate + NADH - Bos taurus ? + NAD+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA1-piperideine 2-carboxylate + NADPH - Bos taurus ? + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA1-piperideine 2-carboxylate + NADPH + H+ - Bos taurus L-pipecolate + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA1-pyrrolidine 2-carboxylate + NADPH + H+ - Bos taurus L-proline + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA2-thiazoline-2-carboxylate + NADPH + H+ - Bos taurus ? + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25lanthionine ketimine + NADH - Bos taurus 1,4-thiomorpholine 3,5-dicarboxylic acid + NAD+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25lanthionine ketimine + NADPH - Bos taurus 1,4-thiomorpholine 3,5-dicarboxylic acid + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25more the non-sulfur substrates exist in equilibrium with open chain forms at low acidic pH. At neutral pH, they exist predominantly as the enzymatically favorable cyclic ketimine form (in which the ring double bond is in the C=N form), while sulfur-containing cyclic ketimine substrates exist predominantly as the enzymatically unfavorable enamine form (in which the ring double bond is in the C=C form) at neutral pH Bos taurus ? - ?
Results 1 - 10 of 52 > >>