Literature DB >> 6871179

S-adenosyl-L-methionine synthetase from human erythrocytes: role in the regulation of cellular S-adenosylmethionine levels.

K L Oden, S Clarke.   

Abstract

The properties of human erythrocyte S-adenosyl-L-methionine synthetase (ATP:L-methionine S-adenosyltransferase, EC 2.5.1.6) were studied with respect to the role of S-adenosylmethionine in transmethylation reactions. Kinetic values obtained with both a cytosolic and a 350-fold purified preparation of enzyme were compared with measured intracellular concentrations of substrates and products. This analysis revealed that effective regulation of enzyme activity and product concentration can occur through feedback inhibition by S-adenosylmethionine (Ki = 2.0-2.9 microM; the endogenous concentration is 3.5 microM). This enzyme can be distinguished from S-adenosylmethionine synthetases found in other tissues and appears to be specialized for its role in erythrocyte methyl group metabolism, especially with regard to protein carboxyl methyl-transfer reactions.

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Year:  1983        PMID: 6871179     DOI: 10.1021/bi00281a030

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  12 in total

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2.  Methionine interference in rapamycin production involves repression of demethylrapamycin methyltransferase and S-adenosylmethionine synthetase.

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3.  Influence of S-adenosylmethionine pool size on spontaneous mutation, dam methylation, and cell growth of Escherichia coli.

Authors:  L M Posnick; L D Samson
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

4.  Methylation of calmodulin at carboxylic acid residues in erythrocytes. A non-regulatory covalent modification?

Authors:  L S Brunauer; S Clarke
Journal:  Biochem J       Date:  1986-06-15       Impact factor: 3.857

5.  Carboxyl methylation of human erythrocyte band 3 in intact cells. Relation to anion transport activity.

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Review 7.  Protein damage and methylation-mediated repair in the erythrocyte.

Authors:  P Galletti; D Ingrosso; C Manna; G Clemente; V Zappia
Journal:  Biochem J       Date:  1995-03-01       Impact factor: 3.857

8.  Co-inhibition of Plasmodium falciparum S-adenosylmethionine decarboxylase/ornithine decarboxylase reveals perturbation-specific compensatory mechanisms by transcriptome, proteome, and metabolome analyses.

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9.  Spontaneous methylation of hemoglobin by S-adenosyl-methionine by a specific and saturable mechanism.

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Review 10.  The impact of cellular metabolism on chromatin dynamics and epigenetics.

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Journal:  Nat Cell Biol       Date:  2017-10-23       Impact factor: 28.824

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