BRENDA - Enzyme Database
show all sequences of 2.3.1.22

Identification, purification, and characterization of monoacylglycerol acyltransferase from developing peanut cotyledons

Tumaney, A.W.; Shekar, S.; Rajasekharan, R.; J. Biol. Chem. 276, 10847-10852 (2001)

Data extracted from this reference:

Activating Compound
Activating Compound
Commentary
Organism
Structure
oleic acid
stimulates below 0.015 mM
Arachis hypogaea
palmitic acid
0.02-0.05 mM, stimulates
Arachis hypogaea
phosphatidic acid
stimulates
Arachis hypogaea
phosphatidylcholine
stimulates
Arachis hypogaea
sphingomyelin
0.0025-0.0075 mM, activates
Arachis hypogaea
sphingosine
0.0025-0.0075 mM, activates
Arachis hypogaea
Inhibitors
Inhibitors
Commentary
Organism
Structure
beta-octylglucoside
40 mM, 50% loss of activity
Arachis hypogaea
CHAPS
20 mM, complete loss of activity
Arachis hypogaea
NaF
-
Arachis hypogaea
Triton X-100
42% loss of activity
Arachis hypogaea
KM Value [mM]
KM Value [mM]
KM Value Maximum [mM]
Substrate
Commentary
Organism
Structure
0.00565
-
1-oleoylglycerol
-
Arachis hypogaea
0.00935
-
oleoyl-CoA
-
Arachis hypogaea
0.01639
-
1-palmitoylglycerol
-
Arachis hypogaea
0.01754
-
palmitoyl-CoA
-
Arachis hypogaea
0.02566
-
stearoyl-CoA
-
Arachis hypogaea
Molecular Weight [Da]
Molecular Weight [Da]
Molecular Weight Maximum [Da]
Commentary
Organism
43000
-
gel filtration
Arachis hypogaea
Natural Substrates/ Products (Substrates)
Natural Substrates
Organism
Commentary (Nat. Sub.)
Natural Products
Commentary (Nat. Pro.)
Organism (Nat. Pro.)
Reversibility
acyl-CoA + sn-2-monoacylglycerol
Arachis hypogaea
diacylglycerol biosynthetic activity
CoA + diacylglycerol
-
-
-
Organism
Organism
Primary Accession No. (UniProt)
Commentary
Textmining
Arachis hypogaea
-
-
-
Purification (Commentary)
Commentary
Organism
-
Arachis hypogaea
Source Tissue
Source Tissue
Commentary
Organism
Textmining
cotyledon
-
Arachis hypogaea
-
Specific Activity [micromol/min/mg]
Specific Activity Minimum [Ámol/min/mg]
Specific Activity Maximum [Ámol/min/mg]
Commentary
Organism
0.0159
-
-
Arachis hypogaea
Substrates and Products (Substrate)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
acyl-CoA + sn-2-monoacylglycerol
diacylglycerol biosynthetic activity
486606
Arachis hypogaea
CoA + diacylglycerol
-
-
-
-
oleoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + 1-palmitoyl-3-oleoyl-sn-glycerol
-
-
-
?
palmitoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
palmitoyl-CoA + sn-1-monooleoylglycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
stearoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
Subunits
Subunits
Commentary
Organism
monomer
1 * 43000, SDS-PAGE
Arachis hypogaea
pH Optimum
pH Optimum Minimum
pH Optimum Maximum
Commentary
Organism
7
-
-
Arachis hypogaea
Activating Compound (protein specific)
Activating Compound
Commentary
Organism
Structure
oleic acid
stimulates below 0.015 mM
Arachis hypogaea
palmitic acid
0.02-0.05 mM, stimulates
Arachis hypogaea
phosphatidic acid
stimulates
Arachis hypogaea
phosphatidylcholine
stimulates
Arachis hypogaea
sphingomyelin
0.0025-0.0075 mM, activates
Arachis hypogaea
sphingosine
0.0025-0.0075 mM, activates
Arachis hypogaea
Inhibitors (protein specific)
Inhibitors
Commentary
Organism
Structure
beta-octylglucoside
40 mM, 50% loss of activity
Arachis hypogaea
CHAPS
20 mM, complete loss of activity
Arachis hypogaea
NaF
-
Arachis hypogaea
Triton X-100
42% loss of activity
Arachis hypogaea
KM Value [mM] (protein specific)
KM Value [mM]
KM Value Maximum [mM]
Substrate
Commentary
Organism
Structure
0.00565
-
1-oleoylglycerol
-
Arachis hypogaea
0.00935
-
oleoyl-CoA
-
Arachis hypogaea
0.01639
-
1-palmitoylglycerol
-
Arachis hypogaea
0.01754
-
palmitoyl-CoA
-
Arachis hypogaea
0.02566
-
stearoyl-CoA
-
Arachis hypogaea
Molecular Weight [Da] (protein specific)
Molecular Weight [Da]
Molecular Weight Maximum [Da]
Commentary
Organism
43000
-
gel filtration
Arachis hypogaea
Natural Substrates/ Products (Substrates) (protein specific)
Natural Substrates
Organism
Commentary (Nat. Sub.)
Natural Products
Commentary (Nat. Pro.)
Organism (Nat. Pro.)
Reversibility
acyl-CoA + sn-2-monoacylglycerol
Arachis hypogaea
diacylglycerol biosynthetic activity
CoA + diacylglycerol
-
-
-
Purification (Commentary) (protein specific)
Commentary
Organism
-
Arachis hypogaea
Source Tissue (protein specific)
Source Tissue
Commentary
Organism
Textmining
cotyledon
-
Arachis hypogaea
-
Specific Activity [micromol/min/mg] (protein specific)
Specific Activity Minimum [Ámol/min/mg]
Specific Activity Maximum [Ámol/min/mg]
Commentary
Organism
0.0159
-
-
Arachis hypogaea
Substrates and Products (Substrate) (protein specific)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
acyl-CoA + sn-2-monoacylglycerol
diacylglycerol biosynthetic activity
486606
Arachis hypogaea
CoA + diacylglycerol
-
-
-
-
oleoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + 1-palmitoyl-3-oleoyl-sn-glycerol
-
-
-
?
palmitoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
palmitoyl-CoA + sn-1-monooleoylglycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
stearoyl-CoA + 1-palmitoyl-sn-glycerol
-
486606
Arachis hypogaea
CoA + ?
-
-
-
?
Subunits (protein specific)
Subunits
Commentary
Organism
monomer
1 * 43000, SDS-PAGE
Arachis hypogaea
pH Optimum (protein specific)
pH Optimum Minimum
pH Optimum Maximum
Commentary
Organism
7
-
-
Arachis hypogaea
Other publictions for EC 2.3.1.22
No.
1st author
Pub Med
title
organims
journal
volume
pages
year
Activating Compound
Application
Cloned(Commentary)
Crystallization (Commentary)
Engineering
General Stability
Inhibitors
KM Value [mM]
Localization
Metals/Ions
Molecular Weight [Da]
Natural Substrates/ Products (Substrates)
Organic Solvent Stability
Organism
Oxidation Stability
Posttranslational Modification
Purification (Commentary)
Reaction
Renatured (Commentary)
Source Tissue
Specific Activity [micromol/min/mg]
Storage Stability
Substrates and Products (Substrate)
Subunits
Temperature Optimum [░C]
Temperature Range [░C]
Temperature Stability [░C]
Turnover Number [1/s]
pH Optimum
pH Range
pH Stability
Cofactor
Ki Value [mM]
pI Value
IC50 Value
Activating Compound (protein specific)
Application (protein specific)
Cloned(Commentary) (protein specific)
Cofactor (protein specific)
Crystallization (Commentary) (protein specific)
Engineering (protein specific)
General Stability (protein specific)
IC50 Value (protein specific)
Inhibitors (protein specific)
Ki Value [mM] (protein specific)
KM Value [mM] (protein specific)
Localization (protein specific)
Metals/Ions (protein specific)
Molecular Weight [Da] (protein specific)
Natural Substrates/ Products (Substrates) (protein specific)
Organic Solvent Stability (protein specific)
Oxidation Stability (protein specific)
Posttranslational Modification (protein specific)
Purification (Commentary) (protein specific)
Renatured (Commentary) (protein specific)
Source Tissue (protein specific)
Specific Activity [micromol/min/mg] (protein specific)
Storage Stability (protein specific)
Substrates and Products (Substrate) (protein specific)
Subunits (protein specific)
Temperature Optimum [░C] (protein specific)
Temperature Range [░C] (protein specific)
Temperature Stability [░C] (protein specific)
Turnover Number [1/s] (protein specific)
pH Optimum (protein specific)
pH Range (protein specific)
pH Stability (protein specific)
pI Value (protein specific)
Expression
General Information
General Information (protein specific)
Expression (protein specific)
KCat/KM [mM/s]
KCat/KM [mM/s] (protein specific)
735610
Yu
Monoacylglycerol O-acyltransfe ...
Homo sapiens
Biochem. Biophys. Res. Commun.
460
715-720
2015
-
-
1
-
1
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1
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4
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3
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1
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1
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1
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1
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3
-
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1
-
-
-
-
-
-
-
-
-
1
4
4
1
-
-
736458
Jin
Diacylglycerol acyltransferase ...
Homo sapiens
J. Biol. Chem.
289
28237-28248
2014
-
-
1
-
-
-
-
-
1
1
3
1
-
2
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-
-
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1
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2
1
1
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-
-
1
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1
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-
-
-
-
-
-
1
1
3
1
-
-
-
-
-
1
-
-
2
1
1
-
-
-
1
-
-
-
-
3
3
-
-
-
735755
Barlind
Identification and design of a ...
Homo sapiens
Bioorg. Med. Chem. Lett.
23
2721-2726
2013
-
2
-
-
-
-
26
-
1
-
-
-
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1
-
-
-
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2
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-
-
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-
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-
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1
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2
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1
26
-
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1
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-
-
-
-
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
1
1
-
-
-
736602
Gao
Intestine-specific expression ...
Homo sapiens, Mus musculus, Mus musculus C57/BL6J
J. Lipid Res.
54
1644-1652
2013
-
-
2
-
2
-
-
-
-
-
-
3
-
5
-
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-
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2
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3
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2
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2
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3
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-
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2
-
-
3
-
-
-
-
-
-
-
-
-
-
3
3
-
-
-
720021
Parthibane
Oleosin is bifunctional enzyme ...
Arachis hypogaea
J. Biol. Chem.
287
1946-1954
2012
-
-
-
-
1
-
-
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1
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4
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1
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2
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1
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1
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1
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1
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-
2
-
-
-
-
-
1
-
-
-
-
1
1
-
-
-
720180
Hall
Evidence for regulated monoacy ...
Homo sapiens
J. Lipid Res.
53
990-999
2012
-
-
-
-
-
-
-
-
-
-
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-
4
-
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1
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3
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1
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1
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-
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-
-
-
3
-
-
3
-
3
-
-
-
3
-
-
-
1
1
1
2
-
-
720755
Vijayaraj
A bifunctional enzyme that has ...
Arachis hypogaea
Plant Physiol.
160
667-683
2012
-
-
-
-
-
-
-
2
-
-
-
-
-
1
-
-
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-
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3
-
1
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-
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-
1
-
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2
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-
-
3
-
1
-
-
-
-
1
-
-
-
1
1
-
-
-
720860
Petrie
Recruiting a new substrate for ...
Arabidopsis thaliana, Mus musculus
PLoS ONE
7
e35214
2012
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2
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2
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2
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2
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2
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-
-
-
-
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-
-
-
-
2
2
-
-
-
720360
Yue
The acyl coenzymeA:monoacylgly ...
Mus musculus, Rattus norvegicus
Lipids
46
513-520
2011
-
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1
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-
-
-
-
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1
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-
7
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2
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1
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1
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1
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1
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2
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1
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1
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-
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-
-
-
-
703312
Holmes
Comparative genomics and prote ...
Danio rerio, Monodelphis domestica
Comp. Biochem. Physiol. D
5
45-54
2010
-
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-
-
-
-
-
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6
4
-
9
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4
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6
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6
4
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-
4
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-
-
-
-
-
-
6
-
4
8
-
-
-
705006
Hiramine
Novel acyl-coenzyme A:monoacyl ...
Mus musculus
J. Lipid Res.
51
1424-1431
2010
-
-
1
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1
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1
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1
1
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3
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6
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4
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1
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1
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1
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1
1
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1
1
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6
-
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4
-
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-
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2
1
1
2
-
-
701625
Shi
Beyond triglyceride synthesis: ...
Mammalia, no activity in Rodentia
Am. J. Physiol. Endocrinol. Metab.
297
0000
2009
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1
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1
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1
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2
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2
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5
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2
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1
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1
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1
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2
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5
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2
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1
3
3
1
-
-
705856
Yen
Deficiency of the intestinal e ...
Mus musculus
Nat. Med.
15
442-446
2009
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1
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1
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1
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3
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3
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2
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1
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1
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1
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3
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2
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-
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2
2
-
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-
659060
Stoveken
The wax ester synthase/acyl co ...
Acinetobacter sp.
J. Bacteriol.
187
1369-1376
2005
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1
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3
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3
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8
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1
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2
1
4
2
1
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1
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1
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3
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3
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1
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2
1
4
2
1
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1
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-
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-
659670
Yen
A human skin multifunctional O ...
Homo sapiens
J. Lipid Res.
46
2388-2397
2005
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1
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1
1
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2
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1
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6
-
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3
-
1
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1
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1
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1
1
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2
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6
-
-
3
-
1
-
-
-
1
-
-
-
-
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-
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-
672340
Orland
Acyl coenzyme A dependent reti ...
Homo sapiens
Biochim. Biophys. Acta
1737
76-82
2005
-
-
-
-
-
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1
-
2
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1
-
1
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1
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2
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1
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1
1
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2
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-
1
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1
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-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
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-
673153
Oxley
-
Enzyme activities of intestina ...
Salmo salar
Comp. Biochem. Physiol. B
141B
77-87
2005
-
-
-
-
-
-
4
-
1
-
-
1
-
1
-
-
-
-
-
2
-
-
1
-
1
-
-
-
1
-
-
-
-
-
-
-
-
-
-
-
-
-
-
4
-
-
1
-
-
1
-
-
-
-
-
2
-
-
1
-
1
-
-
-
1
-
-
-
-
-
-
-
-
-
675260
Yen
The triacylglycerol synthesis ...
Mus musculus
J. Lipid Res.
46
1502-1511
2005
-
-
-
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1
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1
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2
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1
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2
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1
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1
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1
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2
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-
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-
659335
Cao
A predominant role of acyl-CoA ...
Mus musculus
J. Biol. Chem.
279
18878-18886
2004
-
1
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-
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1
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1
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4
-
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-
2
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1
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-
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-
-
-
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-
-
1
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MGAT2, a monoacylglycerol acyl ...
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Human intestinal monoacylglyce ...
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Identification of acyl coenzym ...
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486605
Yen
Identification of a gene encod ...
Mus musculus
Proc. Natl. Acad. Sci. USA
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Identification, purification, ...
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Coleman
Diradylglycerols alter fatty a ...
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Biochemistry
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Loirdighi
Ontogeny and location of HMG-C ...
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Bhat
Sphingosine inhibits rat hepat ...
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Biochemistry
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486609
Mostafa
Adipose monoacylglycerol:acyl- ...
Zonotrichia albicollis
Lipids
29
785-791
1994
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Bhat
Solubilization and partial pur ...
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Lehner
Stereospecificity of monoacylg ...
Rattus norvegicus
Lipids
28
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1993
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Mostafa
Increased hepatic monoacylglyc ...
Rattus norvegicus
Biochim. Biophys. Acta
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1993
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Coleman
Stereospecificity of monoacylg ...
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Coleman
Monoacylglycerol acyltransfera ...
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Manganaro
Rapid isolation of a triacylgl ...
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1985
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Manganaro
Purification and preliminary c ...
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341-347
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486596
Bierbach
Triacylglycerol biosynthesis i ...
Homo sapiens
Digestion
28
138-147
1983
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Manganaro
Radioassay of the stereospecif ...
Rattus norvegicus
Anal. Biochem.
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1982
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Waite
Utilization of serum lipoprote ...
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Biochim. Biophys. Acta
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301-310
1976
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486600
Tietz
Utilization of 2-acyl-sn-glyce ...
Locusta migratoria
Biochim. Biophys. Acta
388
165-170
1975
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486602
Short
A new assay procedure for mono ...
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Biochem. J.
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