PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2519896-3	1989	Purified rat heart FABP bound a maximum of either 2 mol of [1- 14C]palmitoyl coenzyme A (CoA), oleoyl CoA, or oleic acid per mol of FABP as observed by Scatchard analysis.	oleoyl-coenzyme A	95-105	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	19-23
2906022-5	1988	Stearoyl-CoA desaturase activity, responsible for the conversion of stearoyl-CoA to oleoyl-CoA, was absent in both PFDA-dosed rats and their pair-fed controls at Day 14.	oleoyl-coenzyme A	84-94	stearoyl-CoA desaturase	Rattus norvegicus	0-23
16666608-4	1989	The concentration of free oleoyl-CoA in the reaction mixture when the lipase was inhibited by 50% was calculated to be about 21 micromolar.	oleoyl-coenzyme A	26-36	lipase	Ricinus communis	70-76
3720921-2	1986	The apparent Km and Vmax of ACAT with respect to oleoyl-CoA were determined to be 3 microM and 17.7 pmole min-1 mg-1.	oleoyl-coenzyme A	49-59	sterol O-acyltransferase 1	Oryctolagus cuniculus	28-32
3207680-9	1988	Oleoyl-CoA provided partial protection against inactivation by DEP and acetic anhydride, suggesting that the modified histidine is at or near the active site of ACAT.	oleoyl-coenzyme A	0-10	sterol O-acyltransferase 1	Homo sapiens	161-165
3720921-4	1986	The higher Vmax is attributable to the saturation of ACAT with not only oleoyl-CoA, but also cholesterol.	oleoyl-coenzyme A	72-82	sterol O-acyltransferase 1	Oryctolagus cuniculus	53-57
3977941-8	1985	Oleoyl CoA inhibits mixed-function oxidation in the intact liver by acting directly on cytochrome P-450 and by decreasing generation of NADPH via inhibition of key enzymes of the citric acid cycle and the energy-linked transhydrogenase.	oleoyl-coenzyme A	0-10	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	87-103
6436683-6	1984	In contrast, specifically glucose-6-phosphate dehydrogenase was inhibited by oleoyl-CoA.	oleoyl-coenzyme A	77-87	glucose-6-phosphate dehydrogenase	Rattus norvegicus	26-59
6299366-4	1983	Concomitantly, Z-protein addition decreases the extent of binding of radioactively labeled oleoyl-CoA to microsomal membranes.	oleoyl-coenzyme A	91-101	transmembrane BAX inhibitor motif containing 4	Homo sapiens	15-24
27620384-3	2016	With an apparent K m of 17.0 muM, Dga1p has higher affinity for oleoyl-CoA than the only S. cerevisiae acyltransferase previously kinetically characterized, Lpt1p.	oleoyl-coenzyme A	64-74	diacylglycerol O-acyltransferase	Saccharomyces cerevisiae S288C	34-39
7421586-5	1980	Using labeled oleoyl CoA and the endogenous cholesterol as reactants, ACAT was detected in fresh samples of human liver obtained from patients undergoing staging laparotomy for Hodgkin"s disease.	oleoyl-coenzyme A	14-24	carboxylesterase 1	Homo sapiens	70-74
5153-4	1976	In the absence of bovine serum albumin, the delta9 desaturase which converts stearoyl-CoA into oleoyl-CoA, shows a non-linear correlation between enzyme activity and protein concentration.	oleoyl-coenzyme A	95-105	albumin	Rattus norvegicus	25-38
1061066-3	1975	A new analogue of oleoyl-CoA, oleoyl-(1, N6-etheno)-CoA, is a better detergent (critical micelle concentration = 3.2 muM) than oleoyl-CoA (critical micelle concentration = 4.7 muM).	oleoyl-coenzyme A	18-28	latexin	Homo sapiens	117-120
1061066-3	1975	A new analogue of oleoyl-CoA, oleoyl-(1, N6-etheno)-CoA, is a better detergent (critical micelle concentration = 3.2 muM) than oleoyl-CoA (critical micelle concentration = 4.7 muM).	oleoyl-coenzyme A	18-28	latexin	Homo sapiens	176-179
1061066-6	1975	Moreover, since oleoyl-(1,N6-etheno)CoA is a better detergent than oleoyl-CoA, the detergency of oleoyl-CoA is not the sole cause of the fatty acyl-CoA inhibition of citrate synthase.	oleoyl-coenzyme A	97-107	citrate synthase	Homo sapiens	166-182
1061066-7	1975	These results support a physiological role for oleoyl-CoA as a negative effector for citrate synthase.	oleoyl-coenzyme A	47-57	citrate synthase	Homo sapiens	85-101
33207603-2	2020	The MUFAs palmitoleoyl-CoA (16:1n7) and oleoyl-CoA (18:1n9) are the major products of SCD2.	oleoyl-coenzyme A	16-26	stearoyl-Coenzyme A desaturase 2	Mus musculus	86-90
31818461-4	2020	Here, we demonstrate for the first time that N-arachidonoyl dopamine, N-docosahexaenoyl dopamine, N-oleoyl dopamine and N-palmitoyl dopamine exert inverse agonism at GPR6.	oleoyl-coenzyme A	98-106	G protein-coupled receptor 6	Homo sapiens	166-170
31722970-6	2020	TNF-alpha also increased oleoyl-CoA levels, consistent with the increased ACSL3 expression.	oleoyl-coenzyme A	25-35	tumor necrosis factor	Homo sapiens	0-9
31722970-6	2020	TNF-alpha also increased oleoyl-CoA levels, consistent with the increased ACSL3 expression.	oleoyl-coenzyme A	25-35	acyl-CoA synthetase long chain family member 3	Homo sapiens	74-79
29526665-6	2018	Metabolic labeling indicated that each ACSL3 molecule contributed a net gain of 3.1 oleoyl-CoA/s.	oleoyl-coenzyme A	84-94	acyl-CoA synthetase long chain family member 3	Homo sapiens	39-44
28442322-6	2017	T-3764518 inhibited stearoyl-CoA desaturase-catalyzed conversion of stearoyl-CoA to oleoyl-CoA in colorectal cancer HCT-116 cells and their growth.	oleoyl-coenzyme A	84-94	stearoyl-CoA desaturase	Homo sapiens	20-43
16435483-2	1981	Using (1-(14)C)oleoyl-CoA as the labeled substrate, we have proved that the esterification is catalyzed by acyl-CoA: cholesterol acyltransferase (ACAT) existing in the "microsomal fraction" of the mucosal cell.	oleoyl-coenzyme A	15-25	sterol O-acyltransferase 1	Homo sapiens	146-150
7262818-10	1981	We confirmed that delta 6-desaturase differed from delta 9-desaturase, which converted stearoyl-CoA to oleoyl-CoA.	oleoyl-coenzyme A	103-113	fatty acid desaturase 2	Rattus norvegicus	18-36
32433610-5	2020	Here we present the cryo-electron microscopy structure of human DGAT1 in complex with an oleoyl-CoA substrate.	oleoyl-coenzyme A	89-99	diacylglycerol O-acyltransferase 1	Homo sapiens	64-69
32433611-6	2020	A structure obtained with oleoyl-CoA substrate resolved at approximately 3.2 A shows that the CoA moiety binds DGAT1 on the cytosolic side and the acyl group lies deep within a hydrophobic channel, positioning the acyl-CoA thioester bond near an invariant catalytic histidine residue.	oleoyl-coenzyme A	26-36	diacylglycerol O-acyltransferase 1	Homo sapiens	111-116
24406902-5	2014	In vitro, lysophospholipid acyltransferase activity in these strains showed acyl-CoA substrate specificity, as measured by apparent Vmax/Km ratios, to be linolenoyl-CoA>oleoyl-CoA>linoleoyl-CoA>stearoyl-CoA.	oleoyl-coenzyme A	172-182	lysophospholipid acyltransferase	Saccharomyces cerevisiae S288C	10-42
25152299-4	2014	In this study, synthetic peptides corresponding to the predicted binding sites of DGAT1 enzyme were examined using synchrotron radiation circular dichroism spectroscopy, fluorescence emission and adsorption onto lipid monolayers to determine their interactions with substrates associated with triacylglyceride synthesis (oleoyl-CoA and dioleoylglycerol).	oleoyl-coenzyme A	321-331	diacylglycerol O-acyltransferase 1	Homo sapiens	82-87
24142580-10	2014	In vitro studies revealed that oleoyl-CoA increases SHBG production by downregulating PPAR-gamma levels in HepG2 cells.	oleoyl-coenzyme A	31-41	sex hormone binding globulin	Homo sapiens	52-56
24142580-10	2014	In vitro studies revealed that oleoyl-CoA increases SHBG production by downregulating PPAR-gamma levels in HepG2 cells.	oleoyl-coenzyme A	31-41	peroxisome proliferator activated receptor gamma	Homo sapiens	86-96
23265316-4	2013	Enzymatic assays of RcLPAT2 indicate a preference for ricinoleoyl-CoA over other fatty acid thioesters when ricinoleoyl-LPA is used as the acyl acceptor, while oleoyl-CoA is the preferred substrate when oleoyl-LPA is employed.	oleoyl-coenzyme A	59-69	1-acyl-sn-glycerol-3-phosphate acyltransferase 2	Ricinus communis	20-27
23700249-7	2013	Regarding the acyl-CoA donor, RcLPCAT uses monounsaturated fatty acid thioesters, such as oleoyl-CoA (18:1-CoA), as preferred donors, while it has a low activity with saturated fatty acids and shows a poor utilization of ricinoleoyl-CoA (18:1-OH-CoA).	oleoyl-coenzyme A	90-100	lysophospholipid acyltransferase 1	Ricinus communis	30-37
23701211-6	2013	Moreover, we demonstrate that the previously identified selective acylation of iPLA2beta by oleoyl-CoA occurs at C651 thereby indicating the importance of active site architecture for acylation of this enzyme.	oleoyl-coenzyme A	92-102	phospholipase A2 group VI	Homo sapiens	79-88
23701211-7	2013	Collectively, these results identify C651 as a highly reactive nucleophilic residue within the active site of iPLA2beta which is thioesterified by BEL, acylated by oleoyl-CoA, and located in close spatial proximity to the catalytic serine thereby providing important chemical insights on the mechanisms through which BEL inhibits iPLA2beta and the topology of the active site.	oleoyl-coenzyme A	164-174	phospholipase A2 group VI	Homo sapiens	110-119
23013158-1	2013	Stearoyl-CoA desaturase-1 (SCD1) is an endoplasmic reticulum anchored enzyme catalyzing the synthesis of monounsaturated fatty acids, mainly palmytoleyl-CoA and oleyl-CoA.	oleoyl-coenzyme A	147-156	stearoyl-CoA desaturase	Homo sapiens	0-25
23585481-3	2013	Here, we identified compound 122 as a potent and selective inhibitor of human DGAT2, which appeared to act competitively against oleoyl-CoA in vitro.	oleoyl-coenzyme A	129-139	acyl-CoA wax alcohol acyltransferase 1	Homo sapiens	78-83
23013158-1	2013	Stearoyl-CoA desaturase-1 (SCD1) is an endoplasmic reticulum anchored enzyme catalyzing the synthesis of monounsaturated fatty acids, mainly palmytoleyl-CoA and oleyl-CoA.	oleoyl-coenzyme A	147-156	stearoyl-CoA desaturase	Homo sapiens	27-31
22523576-6	2012	Finally, we show that the Arabidopsis thaliana GPAT4 acyltransferase can produce MAG in Saccharomyces cerevisiae using oleoyl-CoA as the acyl-donor.	oleoyl-coenzyme A	119-129	glycerol-3-phosphate acyltransferase 4	Arabidopsis thaliana	47-52
21281576-5	2011	Oleoyl CoA potently inhibits Kir2.1 by antagonizing the specific requirement for PIP(2), and EPC appears to antagonize activation by the nonspecific anionic requirement.	oleoyl-coenzyme A	0-10	potassium inwardly rectifying channel subfamily J member 2	Homo sapiens	29-35
21281576-5	2011	Oleoyl CoA potently inhibits Kir2.1 by antagonizing the specific requirement for PIP(2), and EPC appears to antagonize activation by the nonspecific anionic requirement.	oleoyl-coenzyme A	0-10	prolactin induced protein	Homo sapiens	81-84
20713121-1	2011	Stearoyl-CoA Desaturase 1 (SCD1) is the rate limiting enzyme catalyzing the biosynthesis of monounsaturated fatty acids preferentially from palmitoyl-CoA and stearoyl-CoA forming respectively palmitoleyl-CoA and oleyl-CoA.	oleoyl-coenzyme A	198-207	stearoyl-CoA desaturase	Homo sapiens	0-25
20713121-1	2011	Stearoyl-CoA Desaturase 1 (SCD1) is the rate limiting enzyme catalyzing the biosynthesis of monounsaturated fatty acids preferentially from palmitoyl-CoA and stearoyl-CoA forming respectively palmitoleyl-CoA and oleyl-CoA.	oleoyl-coenzyme A	198-207	stearoyl-CoA desaturase	Homo sapiens	27-31
21670529-6	2011	The Dga1p-immobilized chip surface was analyzed for interactions of Dga1p with oleoyl-CoA, its substrate, and anti-Dga1p IgG, its interacting protein, by SPR.	oleoyl-coenzyme A	79-89	diacylglycerol O-acyltransferase	Saccharomyces cerevisiae S288C	4-9
21670529-6	2011	The Dga1p-immobilized chip surface was analyzed for interactions of Dga1p with oleoyl-CoA, its substrate, and anti-Dga1p IgG, its interacting protein, by SPR.	oleoyl-coenzyme A	79-89	diacylglycerol O-acyltransferase	Saccharomyces cerevisiae S288C	68-73
21670529-6	2011	The Dga1p-immobilized chip surface was analyzed for interactions of Dga1p with oleoyl-CoA, its substrate, and anti-Dga1p IgG, its interacting protein, by SPR.	oleoyl-coenzyme A	79-89	diacylglycerol O-acyltransferase	Saccharomyces cerevisiae S288C	68-73
20610885-5	2010	Many of the microsomes prepared from frozen human livers (N=14) resisted oleoyl-CoA-mediated activation of UDP-glucuronosyltransferase (UGT) activity, including M-6-G formation, which is highly specific to humans.	oleoyl-coenzyme A	73-83	UDP glucuronosyltransferase family 1 member A complex locus	Homo sapiens	107-134
20964445-6	2010	The results show that oleoyl-CoA binds to ACAT1 with K(d) = 1.9 muM and elicits significant structural changes of the protein as manifested by the significantly positive changes in its fluorescence spectrum; stearoyl-CoA elicits a similar spectrum change but much lower in magnitude.	oleoyl-coenzyme A	22-32	acetyl-CoA acetyltransferase 1	Homo sapiens	42-47
19801371-9	2010	Recombinant CGI-58 showed intrinsic fluorescence for tryptophan that was quenched by the addition of 1-oleoyl-lysophosphatidic acid, oleoyl-CoA, arachidonoyl-CoA, and palmitoyl-CoA, but not by lysophosphatidyl choline.	oleoyl-coenzyme A	133-143	abhydrolase domain containing 5, lysophosphatidic acid acyltransferase	Homo sapiens	12-18
20305126-5	2010	Recombinantly expressed hGLYATL2 efficiently conjugated oleoyl-CoA, arachidonoyl-CoA, and other medium- and long-chain acyl-CoAs to glycine.	oleoyl-coenzyme A	56-66	glycine-N-acyltransferase like 2	Homo sapiens	24-32
20610885-5	2010	Many of the microsomes prepared from frozen human livers (N=14) resisted oleoyl-CoA-mediated activation of UDP-glucuronosyltransferase (UGT) activity, including M-6-G formation, which is highly specific to humans.	oleoyl-coenzyme A	73-83	UDP glucuronosyltransferase family 1 member A complex locus	Homo sapiens	136-139
19121948-9	2009	The transcriptionally light-induced ACBP4 and ACBP5, which encode the two largest forms of Arabidopsis ACBPs, bind oleoyl-CoA esters and likely transfer oleoyl-CoAs from the plastids (the site of de novo fatty acid biosynthesis) to the endoplasmic reticulum for the biosynthesis of non-plastidial membrane lipids in Arabidopsis.	oleoyl-coenzyme A	153-164	acyl-CoA binding protein 4	Arabidopsis thaliana	36-41
20009557-3	2009	Recombinant ACBP4 and ACBP5 proteins were observed to bind oleoyl-CoA ester comparably better than recombinant ACBP6, suggesting that ACBP4 and ACBP5 are promising candidates in the trafficking of oleoyl-CoA from the plastids to the endoplasmic reticulum (ER) for the biosynthesis of non-plastidial membrane lipids.	oleoyl-coenzyme A	59-69	acyl-CoA binding protein 4	Arabidopsis thaliana	12-17
20009557-3	2009	Recombinant ACBP4 and ACBP5 proteins were observed to bind oleoyl-CoA ester comparably better than recombinant ACBP6, suggesting that ACBP4 and ACBP5 are promising candidates in the trafficking of oleoyl-CoA from the plastids to the endoplasmic reticulum (ER) for the biosynthesis of non-plastidial membrane lipids.	oleoyl-coenzyme A	59-69	acyl-CoA binding protein 5	Arabidopsis thaliana	22-27
19121948-9	2009	The transcriptionally light-induced ACBP4 and ACBP5, which encode the two largest forms of Arabidopsis ACBPs, bind oleoyl-CoA esters and likely transfer oleoyl-CoAs from the plastids (the site of de novo fatty acid biosynthesis) to the endoplasmic reticulum for the biosynthesis of non-plastidial membrane lipids in Arabidopsis.	oleoyl-coenzyme A	153-164	acyl-CoA binding protein 5	Arabidopsis thaliana	46-51
17537719-2	2007	Here we report that cytochrome c catalyzes the formation of oleoylglycine from oleoyl-CoA and glycine, in the presence of hydrogen peroxide.	oleoyl-coenzyme A	79-89	cytochrome c, somatic	Homo sapiens	20-32
18287005-9	2008	Among them, we characterized three important enzymes with different substrate specificities and tissue distributions; one, termed lysophosphatidylcholine acyltransferase-3 (a mammalian homologue of Drosophila nessy critical for embryogenesis), prefers arachidonoyl-CoA, and the other two enzymes incorporate oleoyl-CoAs to lysophosphatidylethanolamine and lysophosphatidylserine.	oleoyl-coenzyme A	308-319	lysophosphatidylcholine acyltransferase 3	Homo sapiens	130-171
18772128-4	2008	MBOAT1 is a lysophosphatidylserine (lyso-PS) acyltransferase with preference for oleoyl-CoA.	oleoyl-coenzyme A	81-91	membrane bound O-acyltransferase domain containing 1	Homo sapiens	0-6
18772128-5	2008	MBOAT2 also prefers oleoyl-CoA, using lysophosphatidic acid and lysophosphatidylethanolamine as acyl acceptors.	oleoyl-coenzyme A	20-30	membrane bound O-acyltransferase domain containing 2	Homo sapiens	0-6
18252723-15	2008	Specific activity of Ict1p was found to be higher for oleoyl-CoA as compared with palmitoyl- and stearoyl-CoAs.	oleoyl-coenzyme A	54-64	lysophosphatidic acid acyltransferase ICT1	Saccharomyces cerevisiae S288C	21-26
17537719-6	2007	The functional properties of the reaction closely resemble those observed for the ability of cytochrome c to mediate the synthesis of oleamide from oleoyl-CoA and ammonia, in the presence of hydrogen peroxide (Driscoll, W. J., Chaturvedi., S., and Mueller, G. P. (2007) J. Biol.	oleoyl-coenzyme A	148-158	cytochrome c, somatic	Homo sapiens	93-105
17468887-1	2007	Stearoyl-CoA desaturase (SCD) is an enzyme responsible for the production of cis-9, trans-11 conjugated linoleic acid in ruminant fats, and for the synthesis of palmitoleoyl-CoA and oleoyl-CoA.	oleoyl-coenzyme A	167-177	stearoyl-CoA desaturase	Homo sapiens	0-23
17468887-1	2007	Stearoyl-CoA desaturase (SCD) is an enzyme responsible for the production of cis-9, trans-11 conjugated linoleic acid in ruminant fats, and for the synthesis of palmitoleoyl-CoA and oleoyl-CoA.	oleoyl-coenzyme A	167-177	stearoyl-CoA desaturase	Homo sapiens	25-28
17277381-8	2007	These data suggest that replacing monounsaturated with polyunsaturated fat can benefit coronary heart disease by reducing the availability of oleoyl-CoA in the substrate pool of hepatic ACAT2, thereby reducing cholesteryl oleate secretion and accumulation in plasma lipoproteins.	oleoyl-coenzyme A	142-152	acetyl-Coenzyme A acetyltransferase 2	Mus musculus	186-191
16864775-8	2006	LPCAT preferred lysoPC as a substrate over lysoPA, lysoPI, lysoPS, lysoPE, or lysoPG and prefers palmitoyl-CoA to oleoyl-CoA as the acyl donor.	oleoyl-coenzyme A	114-124	lysophosphatidylcholine acyltransferase 1	Homo sapiens	0-5
15980413-4	2005	In this study, we show that in contrast to their stimulatory effect on K(ATP) channels, LC-CoA (e.g. oleoyl-CoA) potently and reversibly inhibits all other Kir channels tested (Kir1.1, Kir2.1, Kir3.4, Kir7.1).	oleoyl-coenzyme A	101-111	potassium inwardly rectifying channel subfamily J member 1	Homo sapiens	177-183
16981434-5	2006	The results showed that in using sn-1,2-DAG, the highest DGAT activity was from the substrate combination of vernoloyl CoA with 1,2-divernoloyl-sn-glycerol, and the lowest was from vernoloyl CoA or oleoyl CoA with 1,2-dioleoyl-sn-glycerol in both V. galamensis and S. laevis.	oleoyl-coenzyme A	198-208	diacylglycerol O-acyltransferase 1C	Glycine max	57-61
16981434-6	2006	Soybean DGAT was more active with oleoyl CoA than vernoloyl CoA, and more active with 1,2-dioleoyl-sn-glycerol when oleoyl CoA was fed.	oleoyl-coenzyme A	34-44	diacylglycerol O-acyltransferase 1C	Glycine max	8-12
15980413-4	2005	In this study, we show that in contrast to their stimulatory effect on K(ATP) channels, LC-CoA (e.g. oleoyl-CoA) potently and reversibly inhibits all other Kir channels tested (Kir1.1, Kir2.1, Kir3.4, Kir7.1).	oleoyl-coenzyme A	101-111	potassium inwardly rectifying channel subfamily J member 2	Homo sapiens	185-191
15980413-4	2005	In this study, we show that in contrast to their stimulatory effect on K(ATP) channels, LC-CoA (e.g. oleoyl-CoA) potently and reversibly inhibits all other Kir channels tested (Kir1.1, Kir2.1, Kir3.4, Kir7.1).	oleoyl-coenzyme A	101-111	potassium inwardly rectifying channel subfamily J member 5	Homo sapiens	193-199
15980413-4	2005	In this study, we show that in contrast to their stimulatory effect on K(ATP) channels, LC-CoA (e.g. oleoyl-CoA) potently and reversibly inhibits all other Kir channels tested (Kir1.1, Kir2.1, Kir3.4, Kir7.1).	oleoyl-coenzyme A	101-111	potassium inwardly rectifying channel subfamily J member 13	Homo sapiens	201-207
15820750-5	2005	Indeed, incubation of cytosol fraction alone with oleate or oleoyl-CoA at 37 degrees C, followed by centrifugation, induces a significant increase (sevenfold) in PAP-1 activity in the pellet fraction.	oleoyl-coenzyme A	60-70	PDGFA associated protein 1	Rattus norvegicus	162-167
15604682-0	2004	ACBP4 and ACBP5, novel Arabidopsis acyl-CoA-binding proteins with kelch motifs that bind oleoyl-CoA.	oleoyl-coenzyme A	89-99	acyl-CoA binding protein 4	Arabidopsis thaliana	0-5
15485873-7	2004	The recombinant human LPGAT1 enzyme recognized various acyl-CoAs and LPGs as substrates but demonstrated clear preference to long chain saturated fatty acyl-CoAs and oleoyl-CoA as acyl donors, which is consistent with the lipid composition of endogenous PGs identified from different tissues.	oleoyl-coenzyme A	166-176	lysophosphatidylglycerol acyltransferase 1	Homo sapiens	22-28
15485873-8	2004	Kinetic analyses of LPGAT1 expressed in COS-7 cells showed that oleoyl-LPG was preferred over palmitoyl-LPG as an acyl receptor, whereas oleoyl-CoA was preferred over lauroyl-CoA as an acyl donor.	oleoyl-coenzyme A	137-147	lysophosphatidylglycerol acyltransferase 1	Homo sapiens	20-26
15152008-6	2004	The recombinant ALCAT1 enzyme recognizes both monolysocardiolipin and dilysocardiolipin as substrates with a preference for linoleoyl-CoA and oleoyl-CoA as acyl donors.	oleoyl-coenzyme A	127-137	lysocardiolipin acyltransferase 1	Mus musculus	16-22
15604682-0	2004	ACBP4 and ACBP5, novel Arabidopsis acyl-CoA-binding proteins with kelch motifs that bind oleoyl-CoA.	oleoyl-coenzyme A	89-99	acyl-CoA binding protein 5	Arabidopsis thaliana	10-15
15604682-9	2004	Both (His)6-ACBP4 and (His)6-ACBP5 bind [14C]oleoyl-CoA with high affinity, [14C]palmitoyl-CoA with lower affinity and did not bind [14C]arachidonyl-CoA.	oleoyl-coenzyme A	45-55	acyl-CoA binding protein 4	Arabidopsis thaliana	12-17
15604682-9	2004	Both (His)6-ACBP4 and (His)6-ACBP5 bind [14C]oleoyl-CoA with high affinity, [14C]palmitoyl-CoA with lower affinity and did not bind [14C]arachidonyl-CoA.	oleoyl-coenzyme A	45-55	acyl-CoA binding protein 5	Arabidopsis thaliana	29-34
15357018-9	2004	When different molecular species of DAG were provided as substrates to the microsomal mixture, the RcDGAT showed a greater preference to catalyze the transfer of oleate from [14C]oleoyl-CoA to diricinolein than to diolein and dipalmitolein.	oleoyl-coenzyme A	174-189	diacylglycerol O-acyltransferase 1	Ricinus communis	99-105
12077311-8	2002	In addition, MGAT activity was proportional to the level of MGAT1 protein expressed, and the amount of diacylglycerol produced depended on the concentration of either of its substrates, oleoyl-CoA or monooleoylglycerol.	oleoyl-coenzyme A	186-196	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	13-17
14561820-2	2003	Here we show that the two types of lipid act by the same mechanism: oleoyl-CoA potently reduced the ATP sensitivity of cardiac (Kir6.2/SUR2A) and pancreatic (Kir6.2/SUR1) KATP channels in a way very similar to PIP2.	oleoyl-coenzyme A	68-78	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	128-134
14561820-2	2003	Here we show that the two types of lipid act by the same mechanism: oleoyl-CoA potently reduced the ATP sensitivity of cardiac (Kir6.2/SUR2A) and pancreatic (Kir6.2/SUR1) KATP channels in a way very similar to PIP2.	oleoyl-coenzyme A	68-78	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	158-164
14561820-2	2003	Here we show that the two types of lipid act by the same mechanism: oleoyl-CoA potently reduced the ATP sensitivity of cardiac (Kir6.2/SUR2A) and pancreatic (Kir6.2/SUR1) KATP channels in a way very similar to PIP2.	oleoyl-coenzyme A	68-78	ATP binding cassette subfamily C member 8	Homo sapiens	165-169
14561820-3	2003	Mutations (R54Q, R176A) in the C- and N-terminus of Kir6.2 that greatly reduced the PIP2 modulation of ATP sensitivity likewise reduced the modulation by oleoyl-CoA, indicating that the two lipids interact with the same site.	oleoyl-coenzyme A	154-164	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	52-58
12767919-6	2003	mLACS preferentially catalyzed the formation of arachidonoyl-CoA more than palmitoyl-CoA or oleoyl-CoA in PC12 cells.	oleoyl-coenzyme A	92-102	acyl-CoA synthetase long-chain family member 6	Mus musculus	0-5
12479568-6	2002	The binding of oleoyl CoA, lysophosphatidic acid, lysophosphatidylcholine, lithocholic acid and taurolithocholate 3-sulphate to LFABP has been studied using the alpha-helical mutants.	oleoyl-coenzyme A	15-25	fatty acid binding protein 1	Homo sapiens	128-133
12730219-6	2003	MGAT2 enzyme expressed in COS-7 cells displayed a broad range of substrate specificity toward fatty acyl-CoA derivatives and monoacylglycerols, among which the highest activities were observed with oleoyl-CoA and rac-1-monolauroylglycerol, respectively.	oleoyl-coenzyme A	198-208	mannoside acetylglucosaminyltransferase 2	Mus musculus	0-5
11404184-4	2001	Under identical experimental conditions, carnitine palmitoyltransferase I (CPT I) of purified rat liver mitochondria has K(d) values of 2.4 and 22.7 microM for oleoyl-CoA and docosahexaenoyl-CoA, respectively.	oleoyl-coenzyme A	160-170	carnitine palmitoyltransferase 1B	Rattus norvegicus	41-73
12056589-3	2002	Therefore, we determined glycerol-3-phosphate acyltransferase (GPAT) and lysophosphatidic acid acyltransferase (LAT) activity in rat T-lymphocyte and liver membrane preparations in the presence of palmitoyl-CoA and oleoyl-CoA with or without BSA.	oleoyl-coenzyme A	215-225	glycerol-3-phosphate acyltransferase, mitochondrial	Rattus norvegicus	25-61
11404184-3	2001	The K(d) values of ACBP for oleoyl-CoA and docosahexaenoyl-CoA are 0.014 and 0.016 microM, respectively.	oleoyl-coenzyme A	28-38	diazepam binding inhibitor	Rattus norvegicus	19-23
11483630-5	2001	Similarly, a tyrosine-to-alanine change in the FYxDWWN motif of Are2p (residues 523-529) produced an enzyme with decreased activity and apparent affinity for oleoyl-CoA.	oleoyl-coenzyme A	158-168	sterol acyltransferase	Saccharomyces cerevisiae S288C	64-69
11404184-4	2001	Under identical experimental conditions, carnitine palmitoyltransferase I (CPT I) of purified rat liver mitochondria has K(d) values of 2.4 and 22.7 microM for oleoyl-CoA and docosahexaenoyl-CoA, respectively.	oleoyl-coenzyme A	160-170	carnitine palmitoyltransferase 1B	Rattus norvegicus	75-80
10601854-4	2000	Their deduced amino acid sequences were then shown to have 40 and 38% identity, respectively, with a murine acyl CoA:diacylglycerol acyltransferase and their expression in are1 are2 or wild-type yeast resulted in a strong increase in the incorporation of oleyl CoA into triacylglycerols.	oleoyl-coenzyme A	255-264	VPS52 GARP complex subunit	Mus musculus	172-176
11284717-9	2001	Purified GPAT depended on exogenous oleoyl-CoA and sn-glycerol-3-phosphate, with the highest activity at approx.	oleoyl-coenzyme A	36-46	glycerol-3-phosphate acyltransferase, mitochondrial	Homo sapiens	9-13
11171165-3	2000	The effect is dependent on the acyl chain length, e.g. lauryl-CoA is less inhibitory than oleoyl-CoA, causing 34 and 68% inhibition respectively of Glc-6-P uptake after 30 s. The inhibition of Glc-6-P and ATP transport is alleviated by addition of an equivalent concentration of acyl-CoA-binding protein (ACBP) or BSA.	oleoyl-coenzyme A	90-100	diazepam binding inhibitor, acyl-CoA binding protein	Homo sapiens	279-303
11171165-3	2000	The effect is dependent on the acyl chain length, e.g. lauryl-CoA is less inhibitory than oleoyl-CoA, causing 34 and 68% inhibition respectively of Glc-6-P uptake after 30 s. The inhibition of Glc-6-P and ATP transport is alleviated by addition of an equivalent concentration of acyl-CoA-binding protein (ACBP) or BSA.	oleoyl-coenzyme A	90-100	diazepam binding inhibitor, acyl-CoA binding protein	Homo sapiens	305-309
11108727-3	2000	In the presence of [(14)C]oleoyl-CoA, LPAAT selectively catalyzes the transformation of LPA and alkyl-LPA into [(14)C]phosphatidic acid.	oleoyl-coenzyme A	26-36	membrane bound O-acyltransferase domain containing 2	Homo sapiens	38-43
10821425-5	2000	The data demonstrated for the first time that SCP-2 increases the aqueous pool of oleoyl-CoA by increasing the aqueous/membrane distribution oleoyl-CoA by 2.4-fold.	oleoyl-coenzyme A	82-92	sterol carrier protein 2	Homo sapiens	46-51
10821425-5	2000	The data demonstrated for the first time that SCP-2 increases the aqueous pool of oleoyl-CoA by increasing the aqueous/membrane distribution oleoyl-CoA by 2.4-fold.	oleoyl-coenzyme A	141-151	sterol carrier protein 2	Homo sapiens	46-51
10601854-4	2000	Their deduced amino acid sequences were then shown to have 40 and 38% identity, respectively, with a murine acyl CoA:diacylglycerol acyltransferase and their expression in are1 are2 or wild-type yeast resulted in a strong increase in the incorporation of oleyl CoA into triacylglycerols.	oleoyl-coenzyme A	255-264	sterol acyltransferase	Saccharomyces cerevisiae S288C	177-181
9219899-2	1997	The ACAT activity is strongly inhibited by different ACBP/oleoyl-CoA complexes depending from the molar ratio of protein and fatty acid-CoA.	oleoyl-coenzyme A	58-68	sterol O-acyltransferase 1	Homo sapiens	4-8
10498408-8	1999	Increasing oleoyl-CoA reversed the inhibition of microsomal ACAT by cholesterol poor (1.4 mol%) liposomes, but did not further stimulate ACAT in the presence of cholesterol rich (35 mol%) liposomes.	oleoyl-coenzyme A	11-21	sterol O-acyltransferase 1	Homo sapiens	60-64
10498408-9	1999	In contrast, high (100 microM) oleoyl-CoA inhibited ACAT nearly 3-fold.	oleoyl-coenzyme A	31-41	sterol O-acyltransferase 1	Homo sapiens	52-56
10498408-12	1999	Concomitantly, under conditions in which SCP-2 stimulated ACAT it equally enhanced transacylation of oleoyl-CoA into phospholipids, and 5.2-fold enhanced oleoyl-CoA transacylation to triacylglycerols.	oleoyl-coenzyme A	101-111	sterol carrier protein 2	Homo sapiens	41-46
9473293-6	1998	Furthermore, mouse ACBP enhanced microsomal phosphatidic acid formation from oleoyl-CoA 2.3-fold.	oleoyl-coenzyme A	77-87	diazepam binding inhibitor	Mus musculus	19-23
9473293-10	1998	Although these small differences in amino acid sequence did not alter binding affinity for cis-parinaroyl-CoA, rat liver ACBP stimulated utilization of oleoyl-CoA 3.8-fold by microsomal glycerol-3-phosphate acyltransferase, significantly higher than that observed with mouse ACBP, but did not alter microsomal phospholipid acyl chain remodeling from oleoyl-CoA.	oleoyl-coenzyme A	152-162	diazepam binding inhibitor	Rattus norvegicus	121-125
9473293-10	1998	Although these small differences in amino acid sequence did not alter binding affinity for cis-parinaroyl-CoA, rat liver ACBP stimulated utilization of oleoyl-CoA 3.8-fold by microsomal glycerol-3-phosphate acyltransferase, significantly higher than that observed with mouse ACBP, but did not alter microsomal phospholipid acyl chain remodeling from oleoyl-CoA.	oleoyl-coenzyme A	152-162	diazepam binding inhibitor	Mus musculus	275-279
9473293-12	1998	Finally, both mouse and rat ACBP shifted the incorporation of oleoyl-CoA from microsomal phospholipid acyl chain remodeling to phosphatidic acid biosynthesis.	oleoyl-coenzyme A	62-72	diazepam binding inhibitor	Rattus norvegicus	28-32
9756869-5	1998	Oleoyl-CoA (1 microM) activated both wild-type Kir6.2/SUR1 and Kir6.2DeltaC36 macroscopic currents, approximately 2-fold, by increasing the number and open probability of Kir6.2/SUR1 and Kir6.2DeltaC36 channels.	oleoyl-coenzyme A	0-10	ATP-binding cassette sub-family C member 8	Xenopus laevis	54-58
9756869-5	1998	Oleoyl-CoA (1 microM) activated both wild-type Kir6.2/SUR1 and Kir6.2DeltaC36 macroscopic currents, approximately 2-fold, by increasing the number and open probability of Kir6.2/SUR1 and Kir6.2DeltaC36 channels.	oleoyl-coenzyme A	0-10	ATP-binding cassette sub-family C member 8	Xenopus laevis	178-182
9219899-2	1997	The ACAT activity is strongly inhibited by different ACBP/oleoyl-CoA complexes depending from the molar ratio of protein and fatty acid-CoA.	oleoyl-coenzyme A	58-68	diazepam binding inhibitor, acyl-CoA binding protein	Homo sapiens	53-57
9219899-6	1997	In binding studies we have characterized binding sites on microsomal membranes for the ACAT substrate oleoyl-CoA and the ACAT inhibitor diazepam.	oleoyl-coenzyme A	102-112	sterol O-acyltransferase 1	Homo sapiens	87-91
9219899-8	1997	This common binding site is suggested to be responsible for the transfer from ACBP-bound oleoyl-CoA to ACAT and, therefore, to be essential for the microsomal cholesterol esterification.	oleoyl-coenzyme A	89-99	diazepam binding inhibitor, acyl-CoA binding protein	Homo sapiens	78-82
9219899-8	1997	This common binding site is suggested to be responsible for the transfer from ACBP-bound oleoyl-CoA to ACAT and, therefore, to be essential for the microsomal cholesterol esterification.	oleoyl-coenzyme A	89-99	sterol O-acyltransferase 1	Homo sapiens	103-107
9143360-7	1997	First, I-FABP decreased microsomal membrane-bound oleoyl-CoA.	oleoyl-coenzyme A	50-60	fatty acid binding protein 2	Rattus norvegicus	7-13
9143360-8	1997	Second, oleoyl-CoA displaced I-FABP bound fluorescent fatty acid, cis-parinaric acid, with Ki of 5.3 microM and 1.1 sites.	oleoyl-coenzyme A	8-18	fatty acid binding protein 2	Rattus norvegicus	29-35
9143360-9	1997	Third, oleoyl-CoA decreased I-FABP tryptophan fluorescence with a Kd of 4.2 microM.	oleoyl-coenzyme A	7-17	fatty acid binding protein 2	Rattus norvegicus	28-34
9143360-10	1997	Fourth, oleoyl-CoA red shifted emission spectra of acrylodated I-FABP, a sensitive marker of I-FABP interactions with ligands.	oleoyl-coenzyme A	8-18	fatty acid binding protein 2	Rattus norvegicus	63-69
9143360-10	1997	Fourth, oleoyl-CoA red shifted emission spectra of acrylodated I-FABP, a sensitive marker of I-FABP interactions with ligands.	oleoyl-coenzyme A	8-18	fatty acid binding protein 2	Rattus norvegicus	93-99
8136369-8	1994	Furthermore, in vitro only L-FABP significantly increases the rate of incorporation of oleoyl-CoA into lysophosphatidic acid and phosphatidic acid.	oleoyl-coenzyme A	87-97	fatty acid binding protein 1	Rattus norvegicus	27-33
8943231-5	1996	Oleoyl-CoA and oleic acid (but not coenzyme A) significantly altered SCP-2 Trp50 emission and anisotropy decay, thereby increasing SCP-2 rotational correlation time, SCP-2 hydrodynamic radius, and SCP-2 Trp50 remaining anisotropy up to 1.7-, 1.2-, and 1.3-fold, respectively.	oleoyl-coenzyme A	0-10	sterol carrier protein 2	Homo sapiens	69-74
8943231-5	1996	Oleoyl-CoA and oleic acid (but not coenzyme A) significantly altered SCP-2 Trp50 emission and anisotropy decay, thereby increasing SCP-2 rotational correlation time, SCP-2 hydrodynamic radius, and SCP-2 Trp50 remaining anisotropy up to 1.7-, 1.2-, and 1.3-fold, respectively.	oleoyl-coenzyme A	0-10	sterol carrier protein 2	Homo sapiens	131-136
8943231-5	1996	Oleoyl-CoA and oleic acid (but not coenzyme A) significantly altered SCP-2 Trp50 emission and anisotropy decay, thereby increasing SCP-2 rotational correlation time, SCP-2 hydrodynamic radius, and SCP-2 Trp50 remaining anisotropy up to 1.7-, 1.2-, and 1.3-fold, respectively.	oleoyl-coenzyme A	0-10	sterol carrier protein 2	Homo sapiens	131-136
8943231-5	1996	Oleoyl-CoA and oleic acid (but not coenzyme A) significantly altered SCP-2 Trp50 emission and anisotropy decay, thereby increasing SCP-2 rotational correlation time, SCP-2 hydrodynamic radius, and SCP-2 Trp50 remaining anisotropy up to 1.7-, 1.2-, and 1.3-fold, respectively.	oleoyl-coenzyme A	0-10	sterol carrier protein 2	Homo sapiens	131-136
8960784-4	1996	Experiments with [3H]cholesterol and [14C]oleoyl-CoA indicated the time course of equilibration of exogenous with endogenous cholesterol as ACAT substrates, and showed that ACAT activity could be accurately measured using [3H]cholesterol/Tween 80, providing that the concentration of endogenous microsomal cholesterol was also determined.	oleoyl-coenzyme A	42-52	carboxylesterase 1	Homo sapiens	173-177
8541331-3	1995	Dissociation constants for binding of oleic acid, arachidonic acid, oleoyl-CoA, lysophosphatidic acid and the peroxisomal proliferator bezafibrate to L-FABP have been determined by titration calorimetry.	oleoyl-coenzyme A	68-78	fatty acid binding protein 1	Bos taurus	150-156
8526865-7	1995	MAGL had no, or negligible, activity towards tri-oleoylglycerol, di-oleoylglycerol, oleoylcholesterol, oleoyl-CoA and phosphatidylcholine; it was inhibited by di-isopropylfluorophosphate, PMSF and diethyl p-nitrophenyl phosphate, suggesting that MAGL is a serine hydrolase.	oleoyl-coenzyme A	103-113	monoglyceride lipase	Homo sapiens	0-4
2264826-7	1990	The addition of oleoyl-CoA to the NADH-reduced membranes resulted in the CN(-)-sensitive partial re-oxidation of cytochrome b5, indicating that electrons from NADH were transferred to the site of desaturation via this cytochrome.	oleoyl-coenzyme A	16-26	cytochrome b5 type A	Homo sapiens	113-126
2266955-6	1990	The binding of stoichiometric amounts of oleoyl CoA was accompanied by a small fluorescence enhancement which suggests that fatty acyl CoAs may interact with other regions of the FABP molecule not involved in fatty acid binding.	oleoyl-coenzyme A	41-51	fatty acid binding protein 2	Rattus norvegicus	179-183
34758300-7	2021	The extrinsic supplementation of Acsbg1-deficient Treg cells with oleoyl-CoA restores the phenotype of the Treg metabolic signature.	oleoyl-coenzyme A	66-76	acyl-CoA synthetase bubblegum family member 1	Homo sapiens	33-39
8130278-3	1994	In the presence of calcium, phosphatidylserine and diacylglycerol, both palmitoyl-CoA (Pal-CoA) and oleoyl-CoA (Ole-CoA) enhanced particulate PK-C activity by approx.	oleoyl-coenzyme A	100-110	proline rich transmembrane protein 2	Homo sapiens	142-146
8130278-3	1994	In the presence of calcium, phosphatidylserine and diacylglycerol, both palmitoyl-CoA (Pal-CoA) and oleoyl-CoA (Ole-CoA) enhanced particulate PK-C activity by approx.	oleoyl-coenzyme A	112-119	proline rich transmembrane protein 2	Homo sapiens	142-146
8130278-6	1994	Partially purified cytosolic PK-C activity was enhanced by 60-70% by 13.5 microM of either Pal-CoA or Ole-CoA.	oleoyl-coenzyme A	102-109	proline rich transmembrane protein 2	Homo sapiens	29-33
8174752-7	1994	Solubilized mitochondrial GPAT retained its very high preference for saturated acyl-CoA substrate (palmitoyl-CoA) and had no activity whatever with any tested concentration of the unsaturated substrate oleoyl-CoA.	oleoyl-coenzyme A	202-212	glycerol-3-phosphate acyltransferase, mitochondrial	Rattus norvegicus	26-30
1356829-1	1992	Hormone-sensitive lipase (HSL) is inhibited in a non-competitive manner by oleoyl CoA, oleic acid and 2-monopalmitoylglycerol, 50% inhibition being observed at concentrations of approx.	oleoyl-coenzyme A	75-85	lipase E, hormone sensitive type	Homo sapiens	0-24
1356829-1	1992	Hormone-sensitive lipase (HSL) is inhibited in a non-competitive manner by oleoyl CoA, oleic acid and 2-monopalmitoylglycerol, 50% inhibition being observed at concentrations of approx.	oleoyl-coenzyme A	75-85	lipase E, hormone sensitive type	Homo sapiens	26-29
1356829-4	1992	Feedback inhibition of HSL by oleoyl CoA and oleic acid may therefore prevent accumulation of free fatty acids and cholesterol in the cell, whereas 2-monoacylglycerol may act as a feedback inhibitor if the capacity of monoacylglycerol lipase is exceeded.	oleoyl-coenzyme A	30-40	lipase E, hormone sensitive type	Homo sapiens	23-26
16737684-4	2006	A maximum activation of about 8-fold over the control was observed at 15 microM oleoyl-CoA, whereas 50 microM or more oleoyl-CoA had an inhibitory effect on UGT function.	oleoyl-coenzyme A	118-128	UDP glycosyltransferase 2 family, polypeptide B	Rattus norvegicus	157-160
16737684-7	2006	N-Ethylmaleimide and 5,5"-dithiobis(2-nitrobenzoic acid) abolished the oleoyl-CoA (15 microM)-dependent activation of microsomal UGT.	oleoyl-coenzyme A	71-81	UDP glycosyltransferase 2 family, polypeptide B	Rattus norvegicus	129-132
34928298-1	2022	Work over the past three decades has greatly advanced our understanding of the regulation of Kir K+ channels by polyanionic lipids of the phosphoinositide (e.g., PIP2) and fatty acid metabolism (e.g., oleoyl-CoA).	oleoyl-coenzyme A	201-211	killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4	Homo sapiens	93-96
34928298-4	2022	We observed activation of members of the TREK, TALK, and THIK subfamilies, with the strongest activation by PIP2 for TRAAK and the strongest activation by oleoyl-CoA for TALK-2.	oleoyl-coenzyme A	155-165	potassium two pore domain channel subfamily K member 2	Homo sapiens	41-45
34928298-4	2022	We observed activation of members of the TREK, TALK, and THIK subfamilies, with the strongest activation by PIP2 for TRAAK and the strongest activation by oleoyl-CoA for TALK-2.	oleoyl-coenzyme A	155-165	potassium two pore domain channel subfamily K member 17	Homo sapiens	170-176