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1 , transport and inter-conversion of [(13)C]S-methylmethionine and [(13)C]methionine in hmt2, mmt and
2 her biologically important sulfonium ions, S-methylmethionine and dimethylsulfonioproprionic acid, ha
3 op of the flower stalk determines the seed S-methylmethionine and methionine phenotype of hmt2 mutant
5 ecules of methionine from homocysteine and S-methylmethionine, and methionine methyltransferase (MMT)
8 e results support a model whereby elevated S-methylmethionine in hmt2 vegetative tissue is transporte
9 n hmt2, mmt and wild-type plants show that S-methylmethionine is a non-essential intermediate in the
10 the expression of a yeast SMM transporter, S-Methylmethionine Permease1 (MMP1, YLL061W), was targeted
13 2)-dependent methionine synthases, E. coli S-methylmethionine-S-homocysteine methyltransferase, and A
15 t is predicted to direct the conversion of S-methylmethionine (SMM) and homocysteine (HCys) to two eq
16 (BHMT-2) is a zinc metalloenzyme that uses S-methylmethionine (SMM) as a methyl donor for the methyla
20 to be synthesized in the chloroplast from S-methylmethionine (SMM) imported from the cytosol, but th
23 thesis, Bhmt2 could utilize its substrate (S-methylmethionine [SMM]) to confer protection against ace
24 alyzes the transfer of a methyl group from S-methylmethionine to l-homocysteine, yielding two molecul
25 catalyzes the formation of methionine from S-methylmethionine using S-adenosylmethionine as a methyl
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