What the reference databases state
Chemical structure
- D-arabinitol is the enantiomer of L-arabinitolCompoundChEBI CHEBI:18333Inferred only
Statements
2 statements
2 statements · 1 reference database · Subject: L-arabinitol · Sources: Human-GEM
- L-arabinitol is converted to L-xyluloseCompoundHuman-GEM MAR08342Inferred only
- L-xylulose is converted to L-arabinitolCompoundHuman-GEM MAR08342Inferred only
Reactions
8 reactions
proton+MAM02337c+NADPH(4-)L-arabinitol+NADP(3-)
Catalysed by AKR7A2 or AKR1B1 or AKR1A1
Reaction pageLeft to rightBalancedEC 1.1.1.21, 1.1.1.2GO:0005829
Human-GEM MAR08341CC BY 4.0Reference data
proton+L-xylulose+NADH(2-)L-arabinitol+NAD(+)
Reaction pageReversibleBalancedGO:0005829
Human-GEM MAR08342CC BY 4.0Reference data
Reaction pageLeft to rightBalancedGO:0005829, GO:0005615
Human-GEM MAR08343CC BY 4.0Reference data
Reaction pageReversibleBalance undeterminableGO:0005615
Human-GEM MAR09241CC BY 4.0Reference data
L-arabinitol+NAD(1-)L-xylulose+NADH(2-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:16381CC BY 4.0Reference data
L-arabinitol+NAD(1-)CHEBI:16880+NADH(2-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:21356CC BY 4.0Reference data
L-arabinitol+NAD(1-)CHEBI:17535+NADH(2-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:25225CC BY 4.0Reference data
L-arabinitol+NADP(3-)CHEBI:17535+NADPH(4-)+hydron
Catalysed by AKR1B1
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:25229CC BY 4.0Reference data