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. 2012 Feb 6;287(13):10032–10038. doi: 10.1074/jbc.M111.324244

TABLE 1.

Metabolites whose levels were significantly changed by SeMet treatment

The mean values of the ratio (T30/T0) from three independent experiments are presented. The metabolic pathways were assigned according to the KEGG database. CoA, γ-glutamylcysteine, homocysteine, and urocanic acid were not detected in cell extracts after SeMet treatment. All compounds detected in CE-TOFMS analysis are listed in supplemental Table S2.

Candidate compounds -Fold Related metabolic pathway
Homoserinelactone 160
1-Aminocyclopropane-1-carboxylic acid 31 Cysteine and methionine metabolism
Propanoate metabolism
GDP-mannose 5.6 Fructose and mannose metabolism
N-Glycan biosynthesis
Amino sugar and nucleotide sugar metabolism
Ribulose 5-phosphate 3.6 Pentose phosphate pathway
Pentose and glucuronate interconversions
Methane metabolism
Riboflavin metabolism
Vitamin B6 metabolism
Glycerophosphocholine 3.1 Glycerophospholipid metabolism
Ether lipid metabolism
Trehalose 6-phosphate 3.1 Starch and sucrose metabolism
Orotidine 5′-monophosphate 0.21 Pyrimidine metabolism
N-Acetylglucosamine 6-phosphate 0.10 Amino sugar and nucleotide sugar metabolism
Reduced glutathione 0.06 Cysteine and methionine metabolism
Glutathione metabolism
CoA NDa Fatty acid metabolism
Pantothenate and CoA biosynthesis
γ-Glutamylcysteine ND Glutathione metabolism
Homocysteine ND Cysteine and methionine metabolism
Sulfur metabolism
Urocanic acid ND Histidine metabolism

a ND, not detected in T30 samples.