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DC Field | Value | Language |
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dc.contributor.author | Kolar, Matthew J. | en_US |
dc.contributor.author | KAMAT, SIDDHESH S. | en_US |
dc.date.accessioned | 2019-04-29T09:25:02Z | |
dc.date.available | 2019-04-29T09:25:02Z | |
dc.date.issued | 2016-08 | en_US |
dc.identifier.citation | Biochemistry, 55 (33), 4636-4641. | en_US |
dc.identifier.issn | Jun-60 | en_US |
dc.identifier.issn | 1520-4995 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2645 | - |
dc.identifier.uri | https://doi.org/10.1021/acs.biochem.6b00565 | en_US |
dc.description.abstract | A recently discovered class of endogenous mammalian lipids, branched fatty acid esters of hydroxy fatty acids (FAHFAs), possesses anti-diabetic and anti-inflammatory activities. Here, we identified and validated carboxyl ester lipase (CEL), a pancreatic enzyme hydrolyzing cholesteryl esters and other dietary lipids, as a FAHFA hydrolase. Variants of CEL have been linked to maturity-onset diabetes of the young, type 8 (MODY8), and to chronic pancreatitis. We tested the FAHFA hydrolysis activity of the CEL MODY8 variant and found a modest increase in activity as compared with that of the normal enzyme. Together, the data suggest that CEL might break down dietary FAHFAs. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.subject | Branched Fatty Acid Esters | en_US |
dc.subject | Hydroxy Fatty Acids | en_US |
dc.subject | MODY8 Protein Carboxyl Ester Lipase | en_US |
dc.subject | Transgenic mice overexpressing | en_US |
dc.subject | Lipidomic profiling | en_US |
dc.subject | 2016 | en_US |
dc.title | Branched Fatty Acid Esters of Hydroxy Fatty Acids Are Preferred Substrates of the MODY8 Protein Carboxyl Ester Lipase | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Biology | en_US |
dc.identifier.sourcetitle | Biochemistry | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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