Limonene-1,2-epoxide hydrolase
From Proteopedia
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| == Structural highlights == | == Structural highlights == | ||
| - | The complex of LEH with the valpromide inhibitor shows the valpromide in the LEH active site forming a <scene name='84/846725/Cv/ | + | The complex of LEH with the valpromide inhibitor shows the valpromide in the LEH active site forming a <scene name='84/846725/Cv/5'>hydrogen bond network</scene>. Water molecule is shown as red sphere.In the LEH hydrolysis mechanism <scene name='84/846725/Cv/4'>residue Asp101 acts as the acid and Asp132 as the base</scene> <ref>PMID:26032250</ref>. | 
| </StructureSection> | </StructureSection> | ||
Revision as of 13:34, 14 June 2020
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3D structures of limonene-1,2-epoxide hydrolase
Updated on 14-June-2020
1nww - ReLEH - Rhodococcus erythropolis
4xbw, 5cf1, 5cf2, 4xbx, 5jpp - ReLEH (mutant)
4xby, 5ck6, 5yqt, 5yng - ReLEH (mutant) + cyclopentene oxide
5gkw - ReLEH (mutant) + cyclopentanediol
4xdv, 4xbt, 5clk, 5jpu - ReLEH (mutant) + cyclohexanediol
1nu3 - ReLEH (mutant) + valpromide
5yao - ReLEH (mutant) + expoxid
4r9k, 4r9l - ReLEH (mutant) + hydroxyhexanamide
5aih, 5aif, 5aii - mlLEH - metagenomic library
5aig - mlLEH + valpromide 
References
- ↑ Hopmann KH, Hallberg BM, Himo F. Catalytic mechanism of limonene epoxide hydrolase, a theoretical study. J Am Chem Soc. 2005 Oct 19;127(41):14339-47. doi: 10.1021/ja050940p. PMID:16218628 doi:http://dx.doi.org/10.1021/ja050940p
- ↑ Arand M, Hallberg BM, Zou J, Bergfors T, Oesch F, van der Werf MJ, de Bont JA, Jones TA, Mowbray SL. Structure of Rhodococcus erythropolis limonene-1,2-epoxide hydrolase reveals a novel active site. EMBO J. 2003 Jun 2;22(11):2583-92. PMID:12773375 doi:http://dx.doi.org/10.1093/emboj/cdg275
- ↑ Ferrandi EE, Sayer C, Isupov MN, Annovazzi C, Marchesi C, Iacobone G, Peng X, Bonch-Osmolovskaya E, Wohlgemuth R, Littlechild JA, Monti D. Discovery and characterization of thermophilic limonene-1,2-epoxide hydrolases from hot spring metagenomic libraries. FEBS J. 2015 May 29. doi: 10.1111/febs.13328. PMID:26032250 doi:http://dx.doi.org/10.1111/febs.13328
