PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30948089-5 2019 The ester bonds can be selectively hydrolyzed by cholesterol esterase (CE), an enzyme secreted by macrophagocytes accumulated at the site of infection, whose concentration is positively related to the severity of the infection. Esters 4-9 carboxyl ester lipase Homo sapiens 49-69 30948089-5 2019 The ester bonds can be selectively hydrolyzed by cholesterol esterase (CE), an enzyme secreted by macrophagocytes accumulated at the site of infection, whose concentration is positively related to the severity of the infection. Esters 4-9 carboxyl ester lipase Homo sapiens 71-73 26250423-14 2015 The ester linkage between the lithocholic acid and fucoxanthin of LevLF was hydrolyzed with cholesterol esterase. Esters 4-9 carboxyl ester lipase Homo sapiens 92-112 28117203-7 2017 It completely blocks the catalytic assembly of CEase and prevents it to participate in ester hydrolysis mechanism. Esters 87-92 carboxyl ester lipase Homo sapiens 47-52 19464305-2 2009 Effective impairment of cholesterol absorption by PE suggests that these esters are hydrolyzed by the pancreatic cholesterol esterase (CEase, EC 3.1.1.13) and the liberated sterol may interfere with cholesterol reducing its intestinal absorption. Esters 73-79 carboxyl ester lipase Homo sapiens 102-133 19464305-2 2009 Effective impairment of cholesterol absorption by PE suggests that these esters are hydrolyzed by the pancreatic cholesterol esterase (CEase, EC 3.1.1.13) and the liberated sterol may interfere with cholesterol reducing its intestinal absorption. Esters 73-79 carboxyl ester lipase Homo sapiens 135-140 14691108-2 2004 This study will test the hypothesis that enzyme activities showing CE and PCE character are found in human saliva at levels sufficient to hydrolyze ester-containing composites important to restorative denstistry. Esters 148-153 carboxyl ester lipase Homo sapiens 67-69 1930149-4 1991 I further examined the reaction kinetics of BAL with water-soluble short-chain esters of p-nitrophenol. Esters 79-85 carboxyl ester lipase Homo sapiens 44-47 12417185-1 2003 Previous investigations have demonstrated that the inflammatory cell derived enzyme, cholesterol esterase (CE) could degrade polyurethanes (PUs) by hydrolyzing ester and urethane bonds. Esters 89-94 carboxyl ester lipase Homo sapiens 107-109 8280776-6 1994 Esters containing 20:4 were hydrolyzed by BSSL as efficiently as 18:1 but this fatty acid also accumulated as diacylglycerol with colipase-dependent lipase. Esters 0-6 carboxyl ester lipase Homo sapiens 42-46 8280776-7 1994 At low bile salt concentrations, as found in duodenal contents of newborns, colipase-dependent lipase was virtually unable to hydrolyze esters of 20:4 and 22:6 whereas BSSL hydrolyzed these esters at appreciable rates. Esters 190-196 carboxyl ester lipase Homo sapiens 168-172 8218286-7 1993 Thus, in the absence of enzyme, 0.002 pmol of cellular ester appeared after 2 h, and its level increased only 3.5-fold after 12 h. However, in the presence of cholesterol esterase, the level of cholesterol ester increased 39-fold in the same time period, indicating that the enzyme-mediated uptake accounts for 10-fold greater ester synthesis than that from basal absorption. Esters 55-60 carboxyl ester lipase Homo sapiens 159-179 1930149-7 1991 The fact that butyrate ester has the optimum acyl chain to be a substrate of BAL can be attributed to its acyl-chain length being long enough for interaction with the active centre of BAL and short enough to provide adequate positioning of the ester bond for transition state complex formation. Esters 23-28 carboxyl ester lipase Homo sapiens 77-80 1930149-7 1991 The fact that butyrate ester has the optimum acyl chain to be a substrate of BAL can be attributed to its acyl-chain length being long enough for interaction with the active centre of BAL and short enough to provide adequate positioning of the ester bond for transition state complex formation. Esters 23-28 carboxyl ester lipase Homo sapiens 184-187 3349096-1 1988 The pancreatic enzyme carboxyl ester lipase (CEL) has been shown to hydrolyse a large number of different esters, including triacylglycerols, cholesteryl esters and retinyl esters with an absolute requirement for bile salts. Esters 106-112 carboxyl ester lipase Homo sapiens 22-43 1676983-1 1991 Carboxyl ester lipase (CEL) is a major component of pancreatic juice and is responsible for the hydrolysis of cholesterol esters as well as a variety of other dietary esters. Esters 122-128 carboxyl ester lipase Homo sapiens 0-21 1676983-1 1991 Carboxyl ester lipase (CEL) is a major component of pancreatic juice and is responsible for the hydrolysis of cholesterol esters as well as a variety of other dietary esters. Esters 122-128 carboxyl ester lipase Homo sapiens 23-26 2246249-2 1990 The hydrolysis of ester substrates in mixed monolayers with 1-palmitoyl-2-oleoylphosphatidylcholine by pancreatic carboxylester lipase (CEL) shows an abrupt increase from less than 10 to 100% when substrate abundance exceeds a critical value (Tsujita, T., Muderhwa, J.M., and Brockman, H.L. Esters 18-23 carboxyl ester lipase Homo sapiens 136-139 2340300-8 1990 The data thus indicate that both lipase-colipase and CEL participate in the hydrolysis of 20:5 and 20:4 ester bonds of dietary triacylglycerol. Esters 104-109 carboxyl ester lipase Homo sapiens 53-56 3349096-1 1988 The pancreatic enzyme carboxyl ester lipase (CEL) has been shown to hydrolyse a large number of different esters, including triacylglycerols, cholesteryl esters and retinyl esters with an absolute requirement for bile salts. Esters 106-112 carboxyl ester lipase Homo sapiens 45-48 3349096-6 1988 Lipase alone did not hydrolyse CO or RP, but CEL did hydrolyse these esters if lipase was present. Esters 69-75 carboxyl ester lipase Homo sapiens 45-48 7151775-3 1982 Cholesterol ester hydrolase (cholesterol esterase, EC 3.1.1.13) does not only act on cholesterol esters, but also on esters of fluorescein. Esters 97-103 carboxyl ester lipase Homo sapiens 29-49