Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
twitter

Escherichia coli K-12 substr. MG1655 Compound: uridine-5'-diphosphate bromoacetol

Superclasses: an aromatic compounda bromoaromatic compound
an organic heterocyclic compoundan organonitrogen heterocyclic compounda diazinea pyrimidine
an organohalogen compoundan organobromine compounda bromoaromatic compound

Chemical Formula: C12H15N2O13P2Br

Molecular Weight: 537.11 Daltons

Monoisotopic Molecular Weight: 537.9389242634 Daltons

uridine-5'-diphosphate bromoacetol compound structure

SMILES: C(Br)C(=O)COP(=O)([O-])OP(=O)([O-])OCC1(OC(C(O)C(O)1)N2(C=CC(=O)NC(=O)2))

InChI: InChI=1S/C12H17BrN2O13P2/c13-3-6(16)4-25-29(21,22)28-30(23,24)26-5-7-9(18)10(19)11(27-7)15-2-1-8(17)14-12(15)20/h1-2,7,9-11,18-19H,3-5H2,(H,21,22)(H,23,24)(H,14,17,20)/p-2/t7-,9-,10-,11-/m1/s1

InChIKey: InChIKey=KUNNVLZBOWEQIC-QCNRFFRDSA-L

Unification Links: PubChem:25203077

Standard Gibbs Free Energy of Formation (ΔfG in kcal/mol): -639.94

Enzymes inhibited by uridine-5'-diphosphate bromoacetol, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: UDP-glucose 4-epimerase [Flentke90]

References

Flentke90: Flentke GR, Frey PA (1990). "Reaction of uridine diphosphate galactose 4-epimerase with a suicide inactivator." Biochemistry 1990;29(9);2430-6. PMID: 2186813


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by Pathway Tools version 19.5 (software by SRI International) on Fri Apr 29, 2016, biocyc11.