EC Number |
Natural Substrates |
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4.1.1.50 | more |
adhesion-dependent expression of S-adenosylmethionine decarboxylase contributes to extracellular matrix-dependent differentiation of human salivary gland epithelial cells |
4.1.1.50 | more |
critical regulatory enzyme of the polyamine biosynthetic pathway |
4.1.1.50 | more |
key enzyme involved in polyamine biosynthetic pathway |
4.1.1.50 | more |
key enzyme of polyamine biosynthetic pathway |
4.1.1.50 | more |
key rate-controlling enzyme in the synthesis of spermidine and spermine. Overexpression of AdoMetDC does not produce an overt cardiac phenotype, but there is an increased cardiac hypertrophy after beta-adrenergic stimulation, and crosses of alpha-myosin heavy chain/ADoMetDC mice with alpha-myosin heavy chain/ornithine decarboxylase mice are lethal at an early embryonic stage |
4.1.1.50 | more |
MdSAMDC1 is mainly involved in fruit development and cell growth |
4.1.1.50 | more |
MdSAMDC2 is mainly involved in stress responses |
4.1.1.50 | more |
S-adenosyl-L-methionine decarboxylase gene of cold-tolerant japonica cultivar Yukihikari and cold-susceptible indica variety TKM9 is differentially expressed under low temperature stress. Upon exposure to cold stress (5°C) the level of OsSAMDC transcripts in the cold-resistant Yukihihari genotype continues to increase for up to 72 h. There is no change in OsSAMDC transcription in the cold-susceptible indica cultivar TLM9 under the same conditions |
4.1.1.50 | more |
synthesis of the triamine spermidine and the tetramine spermine is achieved by the sequential addition of aminopropyl moieties from decarboxylated S-adenosylmethionine, synthesized by the enzyme S-adenosylmethionine decarboxylase |
4.1.1.50 | S-adenosyl-L-methionine |
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