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Escherichia coli K-12 substr. MG1655 Compound Class: a pyrimidine 2'-deoxyribonucleoside

Superclasses: a nucleic acid componenta nucleosidea 2'-deoxynucleoside
a nucleic acid componenta nucleosidea pyrimidine nucleoside
an organic heterocyclic compoundan organonitrogen heterocyclic compounda diazinea pyrimidinea pyrimidine nucleoside

a pyrimidine 2'-deoxyribonucleoside compound structure

Instances:
2'-deoxycytidine,
2'-deoxyuridine,
thymidine

SMILES: C1(C([a pyrimidine base])OC(CO)C(O)1)

Unification Links: ChEBI:68472

Reactions known to consume the compound:

Not in pathways:
a pyrimidine nucleoside + H2O + H+ → a pyrimidine base + D-ribofuranose

Reactions known to produce the compound:

Not in pathways:
a 2'-deoxyribonucleoside 3'-monophosphate[periplasm] + H2O[periplasm]a 2'-deoxynucleoside[periplasm] + phosphate[periplasm]
a 2'-deoxyribonucleoside 5'-monophosphate + H2O → a 2'-deoxynucleoside + phosphate

Not in pathways:
a nucleoside 5'-monophosphate[periplasm] + H2O[periplasm]a nucleoside[periplasm] + phosphate[periplasm]

In Transport reactions:
a nucleoside[extracellular space]a nucleoside[periplasm],
a nucleoside[periplasm] + H+[periplasm]a nucleoside[cytosol] + H+[cytosol]

Enzymes inhibited by a pyrimidine 2'-deoxyribonucleoside, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: acid phosphatase / phosphotransferase [Thaller97]

Credits:
Created 23-Oct-2009 by Kothari A, SRI International


References

Thaller97: Thaller MC, Schippa S, Bonci A, Cresti S, Rossolini GM (1997). "Identification of the gene (aphA) encoding the class B acid phosphatase/phosphotransferase of Escherichia coli MG1655 and characterization of its product." FEMS Microbiol Lett 1997;146(2);191-8. PMID: 9011040


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 Tue May 3, 2016, biocyc14.