Metabolic Modeling Tutorial
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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
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MetaCyc Reaction: 2.4.1.35

Superclasses: Reactions Classified By Conversion Type Simple Reactions Chemical Reactions
Reactions Classified By Substrate Small-Molecule Reactions

EC Number: 2.4.1.35

In Pathway: phenolic malonylglucosides biosynthesis

Note that this reaction equation differs from the official Enzyme Commission reaction equation for this EC number, which can be found here .

The reaction direction shown, that is, A + B ↔ C + D versus C + D ↔ A + B, is in accordance with the Enzyme Commission system.

Most BioCyc compounds have been protonated to a reference pH value of 7.3, and some reactions have been computationally balanced for hydrogen by adding free protons. Please see the PGDB Concepts Guide for more information.

Mass balance status: Balanced.

Enzyme Commission Primary Name: phenol β-glucosyltransferase

Enzyme Commission Synonyms: UDPglucosyltransferase (ambiguous), phenol-β-D-glucosyltransferase, UDP glucosyltransferase (ambiguous), UDP-glucose glucosyltransferase (ambiguous), uridine diphosphoglucosyltransferase

Standard Gibbs Free Energy (ΔrG in kcal/mol): -10.33139 Inferred by computational analysis [Latendresse13]

Enzyme Commission Summary:
Acts on a wide range of phenols.

Citations: [Taguchi10, Dutton66]

Relationship Links: BRENDA:EC:2.4.1.35 , ENZYME:EC:2.4.1.35 , IUBMB-ExplorEnz:EC:2.4.1.35

Credits:
Created 04-Oct-2011 by Dreher KA , PMN


References

Dutton66: Dutton GJ (1966). "Uridine diphosphate glucose and the synthesis of phenolic glucosides by mollusks." Arch Biochem Biophys 116(1);399-405. PMID: 5961845

Latendresse13: Latendresse M. (2013). "Computing Gibbs Free Energy of Compounds and Reactions in MetaCyc."

Taguchi10: Taguchi G, Ubukata T, Nozue H, Kobayashi Y, Takahi M, Yamamoto H, Hayashida N (2010). "Malonylation is a key reaction in the metabolism of xenobiotic phenolic glucosides in Arabidopsis and tobacco." Plant J 63(6);1031-41. PMID: 20626660


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 Fri Nov 21, 2014, BIOCYC14B.