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BRENDA support

Ligand 1-stearoyl-sn-glycerol 3-phosphate

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Basic Ligand Information

Molecular Structure
Picture of 1-stearoyl-sn-glycerol 3-phosphate (click for magnification)
Molecular Formula
BRENDA Name
InChIKey
C21H43O7P
1-stearoyl-sn-glycerol 3-phosphate
LAYXSTYJRSVXIH-HXUWFJFHSA-N
Synonyms:
1-O-octadecyl-sn-glycero-3-phosphatidate, 1-stearoyl-2-hydroxy-sn-glycero-3-phosphate, 1-stearoyl-2-lyso-sn-glycerol 3-phosphate, 1-stearoyl-2-lysophosphatidate, 1-stearoyl-2-lysophosphatidic acid, 1-stearoyl-glycerol 3-phosphate, 1-stearoyl-lysophosphatidic acid, 1-stearoyl-sn-glycerol-3-phosphate, 1-stearoyl-sn-gycerol-3-phosphate, 1-stearoylglycerol 3-phosphate, stearoyl-sn-glycerol-3-phosphate, stearoyl-sn-glycerol 3-phosphate
Pathway Source
Pathways

Roles as Enzyme Ligand

In Vivo Substrate in Enzyme-catalyzed Reactions (2 results)

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

Substrate in Enzyme-catalyzed Reactions (9 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE

Product in Enzyme-catalyzed Reactions (8 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
1-O-octadecyl-sn-glycero-3-phosphocholine + H2O = 1-O-octadecyl-sn-glycero-3-phosphatidate + choline
show the reaction diagram
-

Inhibitor in Enzyme-catalyzed Reactions (2 results)

EC NUMBER
COMMENTARY
LITERATURE
ENZYME 3D STRUCTURE
89.8% residual activity at 4 mM
-
Clarification of the structural importance of acyl chain for the inhibitory effect of lysophosphatidic acid on lysoPLD activity. Lysophosphatidic acids with polyunsaturated acyl chains are more potent than those with saturated acyl chains in the inhibition of serum lysoPLD activity
-

Enzyme Kinetic Parameters

KM Value (2 results)

EC NUMBER
KM VALUE [MM]
KM VALUE MAXIMUM [MM]
COMMENTARY
LITERATURE

Ki Value (2 results)

EC NUMBER
KI VALUE [MM]
KI VALUE MAXIMUM [MM]
COMMENTARY
LITERATURE

References & Links

Links to other databases for 1-stearoyl-sn-glycerol 3-phosphate

ChEBI
PubChem
ChEBI
PubChem