PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
27462083-4	2016	Enzymatic analysis has previously shown that AAD family members possess both stearoyl- and palmitoyl-ACP Delta(9) desaturase activity, including the predominant isoform SUPPRESSOR OF SALICYLIC ACID INSENSITIVE2.	Salicylic Acid	183-197	16:0delta9 desaturase 2	Arabidopsis thaliana	105-124
24687220-8	2014	In addition, the ceramide-modifying enzymes AtFAH1, sphingolipid base hydroxylase 2 (AtSBH2), acyl lipid desaturase 2 (AtADS2) and AtSLD1 were highly expressed under cold stress, and all are likely to be related to AtBI-1 function.	Ceramides	17-25	16:0delta9 desaturase 2	Arabidopsis thaliana	119-125
25822663-8	2015	In contrast, significant reduction of VLC ceramides in the loh1-1 loh3-1 knockdown double mutant and lacking of VLC unsaturated ceramides in the ads2 mutants impaired plant tolerance to both dark and light submergences.	Ceramides	128-137	16:0delta9 desaturase 2	Arabidopsis thaliana	145-149
24687220-9	2014	These findings suggest that AtBI-1 contributes to synthesis of sphingolipids during cold stress by interacting with AtSLD1, AtFAH1, AtSBH2 and AtADS2.	Sphingolipids	63-76	16:0delta9 desaturase 2	Arabidopsis thaliana	143-149
24368335-11	2014	Thus, our findings suggest that SAD6 functions as a Delta9-desaturase, and together with FAD3 it increases the levels of unsaturated fatty acids in crown galls under hypoxia and drought stress conditions.	Fatty Acids, Unsaturated	121-144	16:0delta9 desaturase 2	Arabidopsis thaliana	52-69
23585650-4	2013	Fatty acid composition analysis demonstrated that ads2 mutant plants at 6 C have reduced levels of 16:1, 16:2, 16:3, and 18:3 and higher levels of 16:0 and 18:0 fatty acids compared with the wild type.	Fatty Acids	0-10	16:0delta9 desaturase 2	Arabidopsis thaliana	50-54
23585650-4	2013	Fatty acid composition analysis demonstrated that ads2 mutant plants at 6 C have reduced levels of 16:1, 16:2, 16:3, and 18:3 and higher levels of 16:0 and 18:0 fatty acids compared with the wild type.	Fatty Acids	161-172	16:0delta9 desaturase 2	Arabidopsis thaliana	50-54
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidylglycerols	45-65	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidylglycerols	67-69	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	monogalactosyldiacylglycerol	75-104	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	monogalactosyldiacylglycerol	106-110	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidic Acids	151-168	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidylinositols	170-190	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	phosphatidylethanolamine	192-216	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidylcholines	218-237	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Lysophosphatidylcholines	239-263	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23585650-5	2013	Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglycerol (MGDG) content in ads2 mutants were lower and phosphatidic acid, phosphatidylinositol, phosphatidylethanolamine, phosphatidylcholine, lyso-phosphatidylcholine, and phosphatidylserine were higher than the wild type.	Phosphatidylserines	269-287	16:0delta9 desaturase 2	Arabidopsis thaliana	123-127
23175755-5	2013	Through forward and reverse genetics it was shown that AtADS2 is involved in the synthesis of the 24:1(n-9) and 26:1(n-9) components (X:Y, where X is chain length and Y is number of double bonds) of seed lipids, sphingolipids, and the membrane phospholipids phosphatidylserine, and phosphatidylethanolamine.	Sphingolipids	212-225	16:0delta9 desaturase 2	Arabidopsis thaliana	55-61
23175755-5	2013	Through forward and reverse genetics it was shown that AtADS2 is involved in the synthesis of the 24:1(n-9) and 26:1(n-9) components (X:Y, where X is chain length and Y is number of double bonds) of seed lipids, sphingolipids, and the membrane phospholipids phosphatidylserine, and phosphatidylethanolamine.	Phospholipids	244-257	16:0delta9 desaturase 2	Arabidopsis thaliana	55-61
23175755-5	2013	Through forward and reverse genetics it was shown that AtADS2 is involved in the synthesis of the 24:1(n-9) and 26:1(n-9) components (X:Y, where X is chain length and Y is number of double bonds) of seed lipids, sphingolipids, and the membrane phospholipids phosphatidylserine, and phosphatidylethanolamine.	Phosphatidylserines	258-276	16:0delta9 desaturase 2	Arabidopsis thaliana	55-61
23175755-5	2013	Through forward and reverse genetics it was shown that AtADS2 is involved in the synthesis of the 24:1(n-9) and 26:1(n-9) components (X:Y, where X is chain length and Y is number of double bonds) of seed lipids, sphingolipids, and the membrane phospholipids phosphatidylserine, and phosphatidylethanolamine.	phosphatidylethanolamine	282-306	16:0delta9 desaturase 2	Arabidopsis thaliana	55-61
23175755-8	2013	Overexpression of AtADS2 resulted in a substantial increase in the percentage of glycerolipid and sphingolipids species containing 24:1 and a dramatic increase in the percentage of very-long-chain monounsaturated fatty acids in the acyl-CoA pool.	glycerolipid	81-93	16:0delta9 desaturase 2	Arabidopsis thaliana	18-24
23175755-8	2013	Overexpression of AtADS2 resulted in a substantial increase in the percentage of glycerolipid and sphingolipids species containing 24:1 and a dramatic increase in the percentage of very-long-chain monounsaturated fatty acids in the acyl-CoA pool.	Sphingolipids	98-111	16:0delta9 desaturase 2	Arabidopsis thaliana	18-24
23175755-8	2013	Overexpression of AtADS2 resulted in a substantial increase in the percentage of glycerolipid and sphingolipids species containing 24:1 and a dramatic increase in the percentage of very-long-chain monounsaturated fatty acids in the acyl-CoA pool.	Fatty Acids, Monounsaturated	197-224	16:0delta9 desaturase 2	Arabidopsis thaliana	18-24
23175755-8	2013	Overexpression of AtADS2 resulted in a substantial increase in the percentage of glycerolipid and sphingolipids species containing 24:1 and a dramatic increase in the percentage of very-long-chain monounsaturated fatty acids in the acyl-CoA pool.	Acyl Coenzyme A	236-240	16:0delta9 desaturase 2	Arabidopsis thaliana	18-24
22203212-7	2012	Conversely, the homologs of two Arabidopsis sequences encoding Delta9 acyl-lipid desaturase (AT2G31360, ADS2) and FAD3 desaturase (AT2G29980) were down-regulated in the high-oleic acid strain.	Oleic Acid	174-184	16:0delta9 desaturase 2	Arabidopsis thaliana	104-108