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Escherichia coli K-12 substr. MG1655 Compound: 7,8-dihydromonapterin

Synonyms: DHM, H2-MPt

Superclasses: an organic heterocyclic compoundan organic heterobicyclic compounda pteridinea pterin
an organic heterocyclic compoundan organonitrogen heterocyclic compounda pteridinea pterin


Chemical Formula: C9H13N5O4

Molecular Weight: 255.23 Daltons

Monoisotopic Molecular Weight: 255.0967539317 Daltons

7,8-dihydromonapterin compound structure

SMILES: C1(NC2(N=C(N)NC(=O)C(N=C1C(O)C(O)CO)=2))

InChI: InChI=1S/C9H13N5O4/c10-9-13-7-5(8(18)14-9)12-3(1-11-7)6(17)4(16)2-15/h4,6,15-17H,1-2H2,(H4,10,11,13,14,18)/t4-,6-/m0/s1

InChIKey: InChIKey=YQIFAMYNGGOTFB-NJGYIYPDSA-N

Unification Links: ChEBI:71175, PubChem:45479435

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -114.21

Reactions known to consume the compound:

tetrahydromonapterin biosynthesis :
5,6,7,8-tetrahydromonapterin + NADP+7,8-dihydromonapterin + NADPH + H+

Reactions known to produce the compound:

tetrahydromonapterin biosynthesis :
7,8-dihydromonapterin triphosphate + 3 H2O → 7,8-dihydromonapterin + 3 phosphate + 2 H+

Reactions known to both consume and produce the compound:

Not in pathways:
7,8-dihydroneopterin ↔ 7,8-dihydromonapterin

This compound has been characterized as an alternative substrate of the following enzymes: dihydroneopterin aldolase


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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 Sat Feb 6, 2016, biocyc14.