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Ligand Isoprimeverose

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Basic Ligand Information

Molecular Structure
Picture of Isoprimeverose (click for magnification)
Molecular Formula
BRENDA Name
InChIKey
C11H20O10
Isoprimeverose
QYNRIDLOTGRNML-DRWRGJIVSA-N
Synonyms:
alpha-D-Xyl-(1->6)-beta-D-Glc, Xyl(alpha1-6)Glc
Pathway Source
Pathways

Roles as Enzyme Ligand

In Vivo Product in Enzyme-catalyzed Reactions (3 results)

EC NUMBER
PROVEN IN VIVO REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE

Substrate in Enzyme-catalyzed Reactions (5 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
isoprimeverose + starch = ?
show the reaction diagram
-

Product in Enzyme-catalyzed Reactions (5 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc + [Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc-8-aminonaphthalene-1,3,6-trisulfonic acid = Xyl(alpha1-6)Glc + [Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)[Xyl(alpha1-6)]Glc(beta1-4)Glc-8-aminonaphthalene-1,3,6-trisulfonic acid
show the reaction diagram
-

Enzyme Kinetic Parameters

kcat Value (Turnover Number) (4 results)

EC NUMBER
TURNOVER NUMBER [1/S]
TURNOVER NUMBER MAXIMUM [1/S]
COMMENTARY
LITERATURE
532
-
pH 4.5, 60°C

KM Value (4 results)

EC NUMBER
KM VALUE [MM]
KM VALUE MAXIMUM [MM]
COMMENTARY
LITERATURE
4.03
-
pH 4.5, 60°C

References & Links

Links to other databases for Isoprimeverose

ChEBI
PubChem
ChEBI
PubChem