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BRENDA support

Literature summary for 5.5.1.4 extracted from

  • Loewus, M.W.; Loewus, F.A.; Brillinger, G.U.; Otsuka, H.; Floss, H.G.
    Stereochemistry, of the myo-inositol-1-phosphate synthase reaction (1980), J. Biol. Chem., 255, 11710-11712.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Bos taurus
-
-
-
Lilium longiflorum
-
-
-

Reaction

Reaction Comment Organism Reaction ID
D-glucose 6-phosphate = 1D-myo-inositol 3-phosphate reaction proceeds with stereospecific loss of the pro-6R and incorporation of the pro-6S hydrogen into the product. The ring closure thus occurs in a retention mode at C-6 of the substrate Bos taurus
D-glucose 6-phosphate = 1D-myo-inositol 3-phosphate reaction proceeds with stereospecific loss of the pro-6R and incorporation of the pro-6S hydrogen into the product. The ring closure thus occurs in a retention mode at C-6 of the substrate Lilium longiflorum

Source Tissue

Source Tissue Comment Organism Textmining
pollen
-
Lilium longiflorum
-
testis
-
Bos taurus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
D-Glucose 6-phosphate
-
Bos taurus L-myo-Inositol 1-phosphate
-
?
D-Glucose 6-phosphate
-
Lilium longiflorum L-myo-Inositol 1-phosphate
-
?