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Escherichia coli K-12 substr. MG1655 Compound: dCMP

Synonyms: 2'-deoxycytidine 5'-monophosphate, deoxycytidylate, deoxycytidylic acid, deoxycytidine monophosphate, 2'-deoxycytidine 5'-phosphate, deoxycytidine-phosphate

Superclasses: a nucleic acid componenta nucleotidea 2'-deoxyribonucleotidea 2'-deoxyribonucleoside 5'-monophosphatea pyrimidine 2'-deoxyribonucleoside 5'-monophosphate
a nucleic acid componenta nucleotidea 2'-deoxyribonucleotidea pyrimidine 2'-deoxyribonucleotidea pyrimidine 2'-deoxyribonucleoside 5'-monophosphate
a nucleic acid componenta nucleotidea nucleoside 5'-monophosphatea 2'-deoxyribonucleoside 5'-monophosphatea pyrimidine 2'-deoxyribonucleoside 5'-monophosphate
a nucleic acid componenta nucleotidea pyrimidine nucleotidea pyrimidine 2'-deoxyribonucleotidea pyrimidine 2'-deoxyribonucleoside 5'-monophosphate
an organic heterocyclic compoundan organonitrogen heterocyclic compounda diazinea pyrimidinea pyrimidine nucleotidea pyrimidine 2'-deoxyribonucleotidea pyrimidine 2'-deoxyribonucleoside 5'-monophosphate
an organic heterocyclic compoundan organonitrogen heterocyclic compounda diazinea pyrimidine


Chemical Formula: C9H12N3O7P

Molecular Weight: 305.18 Daltons

Monoisotopic Molecular Weight: 307.05693632969997 Daltons

dCMP compound structure

SMILES: C(C2(C(CC(N1(C(N=C(C=C1)N)=O))O2)O))OP([O-])([O-])=O

InChI: InChI=1S/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(19-8)4-18-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)/p-2/t5-,6+,8+/m0/s1

InChIKey: InChIKey=NCMVOABPESMRCP-SHYZEUOFSA-L

Unification Links: CAS:1032-65-1, ChEBI:57566, ChemSpider:5414501, HMDB:HMDB01202, IAF1260:34352, KEGG:C00239, MetaboLights:MTBLC57566, PubChem:7058169

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -328.31

Reactions known to consume the compound:

pyrimidine deoxyribonucleotide phosphorylation :
ATP + dCMP → ADP + dCDP

Not in pathways:
dCMP + H2O → 2'-deoxycytidine + phosphate

Not in pathways:
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]

Reactions known to produce the compound:

pyrimidine deoxyribonucleotides dephosphorylation :
dCTP + H2O → dCMP + diphosphate + H+

Not in pathways:
DNAn + H2O → (deoxynucleotides)(n-1) + a 2'-deoxyribonucleoside 5'-monophosphate

tRNA processing :
a tRNA precursor with a 5' extension and a long 3' trailer + n H2O → a tRNA precursor with a 5' extension and a short 3' extension + n a nucleoside 5'-monophosphate
a tRNA precursor with a short 3' extension → an uncharged tRNA + n a nucleoside 5'-monophosphate

Not in pathways:
a nucleoside 3',5'-bisphosphate + H2O → a nucleoside 5'-monophosphate + phosphate
a tRNA precursor + H2O → a tRNA + a nucleoside 5'-monophosphate
RNase R degradation substrate RNA + n-1 H2O → n-2 a nucleoside 5'-monophosphate + a diribonucleotide
an oligonucleotide + H2O → n a nucleoside 5'-monophosphate
RNA + n H2O → n a nucleoside 5'-monophosphate
DNAn + n H2O → n a nucleoside 5'-monophosphate
a nucleoside diphosphate + H2O → a nucleoside 5'-monophosphate + phosphate + H+
a RNA-DNA hybrid + n H2O → DNA + n a nucleoside 5'-monophosphate
a nucleoside triphosphate + H2O → a nucleoside 5'-monophosphate + diphosphate + H+
RNase II degradation substrate mRNA + n H2O → n a nucleoside 5'-monophosphate
mutated tRNA + n H2O → n a nucleoside 5'-monophosphate
(deoxynucleotides)(n) + H2O → (deoxynucleotides)(n-1) + a nucleoside 5'-monophosphate

This compound has been characterized as an alternative substrate of the following enzymes: phosphatidylserine synthase, deoxyribonucleoside 5'-monophosphate phosphatase, alkaline phosphatase


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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 Feb 9, 2016, biocyc11.