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MetaCyc Compound: cis-zeatin riboside monophosphate

Synonyms: cZRMP

Superclasses: a secondary metabolite

Citations: [Takei04, Kasahara04]

Chemical Formula: C15H20N5O8P

Molecular Weight: 429.32 Daltons

Monoisotopic Molecular Weight: 431.120599219 Daltons

<i>cis</i>-zeatin riboside monophosphate compound structure

SMILES: CC(CO)=CCNC3(=NC=NC2(N(C1(C(C(C(O1)COP([O-])([O-])=O)O)O))C=NC=23))

InChI: InChI=1S/C15H22N5O8P/c1-8(4-21)2-3-16-13-10-14(18-6-17-13)20(7-19-10)15-12(23)11(22)9(28-15)5-27-29(24,25)26/h2,6-7,9,11-12,15,21-23H,3-5H2,1H3,(H,16,17,18)(H2,24,25,26)/p-2/b8-2-/t9-,11-,12-,15-/m1/s1

InChIKey: InChIKey=IRILMCCKFANGJQ-BAJUWZQUSA-L

Unification Links: KEGG:C16441, PubChem:91819762

Standard Gibbs Free Energy of Formation (ΔfG in kcal/mol): -103.88483Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

cis-zeatin biosynthesis :
cis-zeatin riboside monophosphate + H2O → cis-zeatin riboside + phosphate

Reactions known to produce the compound:

cis-zeatin biosynthesis :
cis-hydroxy-prenyl-tRNA → cis-zeatin riboside monophosphate


References

Kasahara04: Kasahara H, Takei K, Ueda N, Hishiyama S, Yamaya T, Kamiya Y, Yamaguchi S, Sakakibara H (2004). "Distinct isoprenoid origins of cis- and trans-zeatin biosyntheses in Arabidopsis." J Biol Chem 279(14);14049-54. PMID: 14726522

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

Takei04: Takei K, Yamaya T, Sakakibara H (2004). "Arabidopsis CYP735A1 and CYP735A2 encode cytokinin hydroxylases that catalyze the biosynthesis of trans-Zeatin." J Biol Chem 279(40);41866-72. PMID: 15280363


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by Pathway Tools version 19.5 (software by SRI International) on Thu Feb 11, 2016, biocyc14.