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| {{STRUCTURE_1nu3| PDB=1nu3 | SCENE= }} | | {{STRUCTURE_1nu3| PDB=1nu3 | SCENE= }} |
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- | '''Limonene-1,2-epoxide hydrolase in complex with valpromide'''
| + | ===Limonene-1,2-epoxide hydrolase in complex with valpromide=== |
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- | ==Overview==
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- | Epoxide hydrolases are essential for the processing of epoxide-containing compounds in detoxification or metabolism. The classic epoxide hydrolases have an alpha/beta hydrolase fold and act via a two-step reaction mechanism including an enzyme-substrate intermediate. We report here the structure of the limonene-1,2-epoxide hydrolase from Rhodococcus erythropolis, solved using single-wavelength anomalous dispersion from a selenomethionine-substituted protein and refined at 1.2 A resolution. This enzyme represents a completely different structure and a novel one-step mechanism. The fold features a highly curved six-stranded mixed beta-sheet, with four alpha-helices packed onto it to create a deep pocket. Although most residues lining this pocket are hydrophobic, a cluster of polar groups, including an Asp-Arg-Asp triad, interact at its deepest point. Site-directed mutagenesis supports the conclusion that this is the active site. Further, a 1.7 A resolution structure shows the inhibitor valpromide bound at this position, with its polar atoms interacting directly with the residues of the triad. We suggest that several bacterial proteins of currently unknown function will share this structure and, in some cases, catalytic properties.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_12773375}}, adds the Publication Abstract to the page |
| + | (as it appears on PubMed at http://www.pubmed.gov), where 12773375 is the PubMed ID number. |
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| + | {{ABSTRACT_PUBMED_12773375}} |
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| ==About this Structure== | | ==About this Structure== |
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| [[Category: Zou, J.]] | | [[Category: Zou, J.]] |
| [[Category: Protein-ligand complex]] | | [[Category: Protein-ligand complex]] |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 02:58:47 2008'' | + | |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 01:45:39 2008'' |
Revision as of 22:45, 28 July 2008
Template:STRUCTURE 1nu3
Limonene-1,2-epoxide hydrolase in complex with valpromide
Template:ABSTRACT PUBMED 12773375
About this Structure
1NU3 is a Single protein structure of sequence from Rhodococcus erythropolis. Full crystallographic information is available from OCA.
Reference
Structure of Rhodococcus erythropolis limonene-1,2-epoxide hydrolase reveals a novel active site., Arand M, Hallberg BM, Zou J, Bergfors T, Oesch F, van der Werf MJ, de Bont JA, Jones TA, Mowbray SL, EMBO J. 2003 Jun 2;22(11):2583-92. PMID:12773375
Page seeded by OCA on Tue Jul 29 01:45:39 2008
Categories: Limonene-1,2-epoxide hydrolase | Rhodococcus erythropolis | Single protein | Arand, M. | Bergfors, T. | Bont, J A.M de. | Hallberg, B M. | Jones, T A. | Mowbray, S L. | Oesch, F. | Werf, M J.van der. | Zou, J. | Protein-ligand complex