2o7v: Difference between revisions
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New page: left|200px<br /><applet load="2o7v" size="350" color="white" frame="true" align="right" spinBox="true" caption="2o7v, resolution 2.30Å" /> '''Carboxylesterase AeC... |
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==Overview== | ==Overview== | ||
Carboxylesterases (CXEs) are widely distributed in plants, where they have | Carboxylesterases (CXEs) are widely distributed in plants, where they have been implicated in roles that include plant defense, plant development, and secondary metabolism. We have cloned, overexpressed, purified, and crystallized a carboxylesterase from the kiwifruit species Actinidia eriantha (AeCXE1). The structure of AeCXE1 was determined by X-ray crystallography at 1.4 A resolution. The crystal structure revealed that AeCXE1 is a member of the alpha/beta-hydrolase fold superfamily, most closely related structurally to the hormone-sensitive lipase subgroup. The active site of the enzyme, located in an 11 A deep hydrophobic gorge, contains the conserved catalytic triad residues Ser169, Asp276, and His306. Kinetic analysis using artificial ester substrates showed that the enzyme can hydrolyze a range of carboxylester substrates with acyl groups ranging from C2 to C16, with a preference for butyryl moieties. This preference was supported by the discovery of a three-carbon acyl adduct bound to the active site Ser169 in the native structure. AeCXE1 was also found to be inhibited by organophosphates, with paraoxon (IC50 = 1.1 muM) a more potent inhibitor than dimethylchlorophosphate (DMCP; IC50 = 9.2 muM). The structure of AeCXE1 with paraoxon bound was determined at 2.3 A resolution and revealed that the inhibitor binds covalently to the catalytic serine residue, with virtually no change in the structure of the enzyme. The structural information for AeCXE1 provides a basis for addressing the wider functional roles of carboxylesterases in plants. | ||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
High- | High-resolution crystal structure of plant carboxylesterase AeCXE1, from Actinidia eriantha, and its complex with a high-affinity inhibitor paraoxon., Ileperuma NR, Marshall SD, Squire CJ, Baker HM, Oakeshott JG, Russell RJ, Plummer KM, Newcomb RD, Baker EN, Biochemistry. 2007 Feb 20;46(7):1851-9. Epub 2007 Jan 26. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17256879 17256879] | ||
[[Category: Actinidia eriantha]] | [[Category: Actinidia eriantha]] | ||
[[Category: Carboxylesterase]] | [[Category: Carboxylesterase]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Baker, E | [[Category: Baker, E N.]] | ||
[[Category: Baker, H | [[Category: Baker, H M.]] | ||
[[Category: Ileperuma, N | [[Category: Ileperuma, N R.]] | ||
[[Category: Marshall, S | [[Category: Marshall, S D.]] | ||
[[Category: Newcomb, R | [[Category: Newcomb, R D.]] | ||
[[Category: Oakeshott, J | [[Category: Oakeshott, J G.]] | ||
[[Category: Plummer, K | [[Category: Plummer, K M.]] | ||
[[Category: Russell, R | [[Category: Russell, R J.]] | ||
[[Category: Squire, C | [[Category: Squire, C J.]] | ||
[[Category: DEP]] | [[Category: DEP]] | ||
[[Category: actinidia eriantha]] | [[Category: actinidia eriantha]] | ||
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[[Category: paraoxon]] | [[Category: paraoxon]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:15:26 2008'' | ||