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S-Adenosyl-L-methionine analogs

Kauss (39) has shown that the esterification of the carboxyl groups in the D-galacturonic acid chain takes place by a transfer of the methyl groups from S-adenosyl-L-methionine, analogous to the case in which the 4-methyl ether groups are transferred to D-glucuronic acid of hemi-cellulose (40). [Pg.379]

Chem. Biol, 2, 31-32 (b) Dalhoff, C., LukinaviJius, G., KlimaSauskas, S., and Weinhold, E. (2005) Synthesis of S-adenosyl-L-methionine analogs and their use for sequence-specific transalkylation of DNA by methyltransferases. Nature Pratoc., 1, 1879-1886. [Pg.421]


See other pages where S-Adenosyl-L-methionine analogs is mentioned: [Pg.830]    [Pg.401]   


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