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Literature summary for 1.1.1.143 extracted from

  • Ruis, H.; Hoffmann-Ostendorf, O.
    Enzymic epimerization of sequoyitol to D-pinitol in Trifolium incarnatum (1969), Eur. J. Biochem., 7, 442-448.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
DTT 5fold activation Trifolium incarnatum
GSH 5fold activation Trifolium incarnatum
L-cysteine 5fold activation at 1.3 mM Trifolium incarnatum

General Stability

General Stability Organism
very unstable Trifolium incarnatum

Inhibitors

Inhibitors Comment Organism Structure
iodoacetate 85% inhibition at 1 mM Trifolium incarnatum
p-chloromercuribenzoate complete inhibition at 1 mM Trifolium incarnatum
Phenylmercurinitrate complete inhibition at 1 mM Trifolium incarnatum

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
34000
-
gel filtration Trifolium incarnatum

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
5-O-methyl-myo-inositol + NAD+ Trifolium incarnatum B-specificity 5D-5-O-methyl-2,3,5/4,6-pentahydroxycyclohexanone + NADH
-
r

Organism

Organism UniProt Comment Textmining
Trifolium incarnatum
-
-
-

Purification (Commentary)

Purification (Comment) Organism
partial Trifolium incarnatum

Source Tissue

Source Tissue Comment Organism Textmining
plant prior to the formation of flowers Trifolium incarnatum
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2,4,6/3,5-pentahydroxycyclohexanone + NADH
-
Trifolium incarnatum ? + NAD+
-
?
5-O-methyl-myo-inositol + NAD+ B-specificity Trifolium incarnatum 5D-5-O-methyl-2,3,5/4,6-pentahydroxycyclohexanone + NADH
-
r
DL-2,3,4,6/5-pentahydroxycyclohexanone + NADH low activity Trifolium incarnatum ? + NAD+
-
?

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
5 9
-
Trifolium incarnatum

Cofactor

Cofactor Comment Organism Structure
NADH
-
Trifolium incarnatum