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0.097
1-alkyl-sn-glycero-3-phosphocholine
-
pH 7.4, 37°C
0.1
1-alkyl-sn-glycero-3-phosphoethanolamine
-
achieved under optimal assay conditions, almost same results in blood plasma
0.0083
1-linoleoyl-2-lyso-glycerophoshorylcholine
-
Vmax is 0.019 micromol/min/mg
0.32
1-O-alkyl-sn-glycero-3-phosphocholine
pH 7.4, temperature not specified in the publication
0.0267
1-O-hexadecyl-2-lyso-glycerophosphorylcholine
-
Vmax is 0.29 micromol/min/mg, lysoPLD activity is more than twice that observed with 1-palmitoyl-glycerophoshorylcholine
0.0207
1-palmitoyl-2-lyso-glycerophoshorylcholine
-
Vmax is 0.059 micromol/min/mg
0.176
1-palmitoyl-glycerophoshorylcholine
-
Vmax is 0.3 micromol/min/mg, best substrate
0.101
1-stearoyl-2-lyso-glycerophoshorylcholine
-
Vmax is 0.035 micromol/min/mg
0.7 - 5.6
4-nitrophenyl-TMP
0.0063
5-[[(23R)-33-(4-[[4-(dimethylamino)phenyl]diazenyl]phenyl)-20,23-dihydroxy-20-oxido-15,33-dioxo-3,6,9,12,19,21,25-heptaoxa-16,32-diaza-20-phosphatritriacont-1-yl]carbamoyl]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acid
-
-
0.004
coumarin-phosphate-fluorescein
-
coumarin-phosphate-fluorescein is a fluorescence resonance energy transfer (FRET)-based sensor of phosphodiesterase activity. Very useful substrate for enzymatic analysis of purified autotaxin/lysoPLD and can also be used to detect autotaxin/lysoPLD activity in serum-free conditioned culture medium isolated from cells expressing the enzyme
0.094 - 1
lysophosphatidylcholine
0.066 - 0.126
lysophosphatidylcholine 16:0
0.089 - 0.27
lysophosphatidylcholine 18:0
0.069 - 0.126
lysophosphatidylcholine 18:1
0.004
[5-[[(23S)-33-(4-[(E)-[4-(dimethylamino)phenyl]diazenyl]phenyl)-20,23-dihydroxy-20-oxido-15,26,33-trioxo-3,6,9,12,19,21,25-heptaoxa-16,32-diaza-20-phosphatritriacont-1-yl]carbamoyl]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)phenyl]acetic acid
-
[5-[[(23S)-33-(4-[(E)-[4-(dimethylamino)phenyl]diazenyl]phenyl)-20,23-dihydroxy-20-oxido-15,26,33-trioxo-3,6,9,12,19,21,25-heptaoxa-16,32-diaza-20-phosphatritriacont-1-yl]carbamoyl]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)phenyl]acetic acid can be used to detect autotaxin/lysoPLD activity in human and mouse blood
additional information
additional information
-
0.7
4-nitrophenyl-TMP
-
wild type enzyme, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
4.8
4-nitrophenyl-TMP
-
mutant enzyme H226Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
5.6
4-nitrophenyl-TMP
-
-
0.0026
FS-3
-
wild type enzyme, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.019
FS-3
-
mutant enzyme H226Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.094
lysophosphatidylcholine
-
-
0.1
lysophosphatidylcholine
-
kinetic analysis of recombinant autotaxin/lysoPLD using [14C] lysophosphatidylcholine substrate
0.15
lysophosphatidylcholine
-
-
0.47
lysophosphatidylcholine
-
in presence of 0.25 mM Zn2+ plus 10 mM L-histidine
0.49
lysophosphatidylcholine
-
-
0.55
lysophosphatidylcholine
-
in presence of 0.25 mM Zn2+
0.66
lysophosphatidylcholine
-
in presence of 10 mM L-histidine
1
lysophosphatidylcholine
pH 7.4, temperature not specified in the publication
0.066
lysophosphatidylcholine 16:0
-
wild type enzyme, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.094
lysophosphatidylcholine 16:0
-
mutant enzyme H420Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.12
lysophosphatidylcholine 16:0
-
mutant enzyme H434Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.126
lysophosphatidylcholine 16:0
-
mutant enzyme H226Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.089
lysophosphatidylcholine 18:0
-
wild type enzyme, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.115
lysophosphatidylcholine 18:0
-
mutant enzyme H420Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.27
lysophosphatidylcholine 18:0
-
mutant enzyme H226Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.069
lysophosphatidylcholine 18:1
-
mutant enzyme H420Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.073
lysophosphatidylcholine 18:1
-
wild type enzyme, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.105
lysophosphatidylcholine 18:1
-
mutant enzyme H434Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
0.126
lysophosphatidylcholine 18:1
-
mutant enzyme H226Q, in 50 mM Tris pH 7.4, 5 mM CaCl2, 1 mg/ml bovine serum albumin, at 37°C
additional information
additional information
-
suggestion that lysoPLD predominantly utilizes saturated forms of lysophosphatidylcholine
-
additional information
additional information
-
affinity for lysophosphatidylcholine is significantly higher than for nucleotides
-
additional information
additional information
-
capable of hydrolyzing sphingosylphosphorylcholine with a significantly higher km-value, also able to hydrolyze nucleotide triphosphates di-adenosine polyphosphates and artificial phosphodiester substrates such as p-nitrophenyl thymidine phosphate with Km-values close to 1 and optimal activity observed at alkaline pH
-
additional information
additional information
-
steady-state, single-turnover, and transient kinetics, kinetic analysis and modeling, using artificial fluorescent substrate FS-3, overview
-