Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
twitter

MetaCyc Enzyme: cysteine-S-conjugate N-malonyl transferase

Species: Arabidopsis thaliana col

Gene-Reaction Schematic: ?

Credits:
Created 03-Aug-2011 by Zhang P , PMN


Enzymatic reaction of: cysteine-S-conjugate N-malonyl transferase

EC Number: 2.3.1.-

an L-cysteine-S-conjugate + malonyl-CoA <=> an N-malonyl-L-cysteine-S-conjugate + coenzyme A + H+

The reaction direction shown, that is, A + B ↔ C + D versus C + D ↔ A + B, is in accordance with the direction in which it was curated.

The reaction is favored in the direction shown.

In Pathways: glutathione-mediated detoxification II

Summary:
A measurable cysteine-S-conjugate N-malonyl transferase activity was detected in crude protein extract from Arabidopsis cell suspension culture. N-malonylation was shown towards fenclorim cysteine-S-conjugate. When the cell culture was treated with 100 uM fenclorim for 24 hours, the enzyme activity was found increased 30-fold [BrazierHicks08].

No gene has been identified for this enzyme activity.


References

BrazierHicks08: Brazier-Hicks M, Evans KM, Cunningham OD, Hodgson DR, Steel PG, Edwards R (2008). "Catabolism of glutathione conjugates in Arabidopsis thaliana. Role in metabolic reactivation of the herbicide safener fenclorim." J Biol Chem 283(30);21102-12. PMID: 18522943


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 18.5 on Wed Dec 17, 2014, biocyc12.