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Results 1 - 9 of 9
EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22more levels of spermidine and spermine are not only regulated by activity of spermidine synthase and spermine synthase, but also by other factors, e.g. the level of aminopropyl donor substrate, overview
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22more The predominant polyamines in mammalian cells are spermidine and spermine, these polyamines are made by the sequential addition of aminopropyl groups from decarboxylated S-adenosylmethionine.
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22more spermine synthase is clearly essential for mammalia
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22more spermine synthase is clearly essential for normal development in humans
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22S-adenosyl 3-(methylthio)propylamine + spermidine -
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22S-adenosylmethioninamine + spermidine involved in polyamine biosynthetic pathway
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22S-adenosylmethioninamine + spermidine the enzyme, which is involved in the polyamine biosynthetic pathway in producing the final product spermine, is not essential for plant survival under normal growth conditions
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22S-adenosylmethioninamine + spermidine Polyamine sythesis, addition of a second aminopropyl group to the N-10 position of spermidine. The active site with a bound spermidine molecule contains an Asp276 residue, which is in an ideal position to facilitate the deprotonation of the N-10 amino group of spermidine that attacks the C-atom of the aminopropyl group of decarboxylated S-adenosylmethionine
Show all pathways known for 2.5.1.22Display the word mapDisplay the reaction diagram Show all sequences 2.5.1.22S-adenosylmethioninamine + spermidine decarboxylated S-adenosylmethionine is an essential intermediate in the synthesis of polyamines
Results 1 - 9 of 9