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Escherichia coli K-12 substr. MG1655 Compound: D-ribulose

Synonyms: D-erythro-pentulose, D-erythropentulose, erythropentulose

Superclasses: all carbohydratesa carbohydratea glycana sugara monosaccharidea pentosea D-pentose
all carbohydratesa carbohydratea glycana sugara monosaccharidea pentoseribulose


Chemical Formula: C5H10O5

Molecular Weight: 150.13 Daltons

Monoisotopic Molecular Weight: 150.0528234315 Daltons

D-ribulose compound structure

SMILES: C(O)C(O)C(O)C(=O)CO

InChI: InChI=1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h3,5-8,10H,1-2H2/t3-,5-/m1/s1

InChIKey: InChIKey=ZAQJHHRNXZUBTE-NQXXGFSBSA-N

Unification Links: CAS:5556-48-9, ChEBI:17173, ChemSpider:133316, HMDB:HMDB00621, KEGG:C00309, MetaboLights:MTBLC17173, PubChem:151261

Standard Gibbs Free Energy of Formation (ΔfG in kcal/mol): -181.0

Reactions known to consume the compound:

D-arabinose degradation I :
D-ribulose + ATP → D-ribulose 1-phosphate + ADP + H+

Reactions known to produce the compound:

Not in pathways:
a sugar phosphate + H2O → a sugar + phosphate

Reactions known to both consume and produce the compound:

D-arabinose degradation I :
D-arabinopyranose ↔ D-ribulose

In Transport reactions:
a monosaccharide[periplasm]a monosaccharide[extracellular space],
a [PTS enzyme I]-Nπ-phospho-L-histidine + a sugar[periplasm] → a [PTS enzyme I]-L-histidine + a sugar phosphate[cytosol]

This compound has been characterized as an alternative substrate of the following enzymes: L-fuculokinase, L-ribulokinase


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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 Wed May 4, 2016, biocyc13.