MetaCyc Compound: N-acetyl-D-mannosamine 6-phosphate

Synonyms: ManNAc-6-P, N-acetylmannosamine-6-P, N-acetyl-mannosamine-6-P, N-acetyl-D-mannosamine-6-P, N-acetyl-mannosamine 6-phosphate

Superclasses: an N-acyl-alpha-D-mannosamine 6-phosphate

Chemical Formula: C8H14NO9P

Molecular Weight: 299.17 Daltons

Monoisotopic Molecular Weight: 301.0562676277 Daltons

<i>N</i>-acetyl-D-mannosamine 6-phosphate compound structure

SMILES: CC(=O)NC1(C(O)OC(COP([O-])(=O)[O-])C(O)C(O)1)

InChI: InChI=1S/C8H16NO9P/c1-3(10)9-5-7(12)6(11)4(18-8(5)13)2-17-19(14,15)16/h4-8,11-13H,2H2,1H3,(H,9,10)(H2,14,15,16)/p-2/t4-,5+,6-,7-,8?/m1/s1


Unification Links: ChEBI:28273, HMDB:HMDB01121, IAF1260:43459, KEGG:C04257, PubChem:54758653

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -282.58258Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

CMP-N-acetylneuraminate biosynthesis I (eukaryotes) :
phosphoenolpyruvate + N-acetyl-D-mannosamine 6-phosphate + H2O → N-acetyl-β-neuraminate 9-phosphate + phosphate

Reactions known to produce the compound:

CMP-N-acetylneuraminate biosynthesis I (eukaryotes) , N-acetylneuraminate and N-acetylmannosamine degradation I :
N-acetyl-D-mannosamine + ATP → N-acetyl-D-mannosamine 6-phosphate + ADP + H+

Reactions known to both consume and produce the compound:

N-acetylneuraminate and N-acetylmannosamine degradation I :
N-acetyl-D-mannosamine 6-phosphateN-acetyl-D-glucosamine 6-phosphate

In Reactions of unknown directionality:

Not in pathways:
an N-acyl-D-glucosamine 6-phosphate = an N-acyl-α-D-mannosamine 6-phosphate
an N-acyl-D-mannosamine + ATP = an N-acyl-α-D-mannosamine 6-phosphate + ADP + H+


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

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Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
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