1hqd
From Proteopedia
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, resolution 2.30Å | |||||||
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Ligands: | , | ||||||
Activity: | Triacylglycerol lipase, with EC number 3.1.1.3 | ||||||
Related: | 3LIP, 1OIL, 2LIP, 4LIP, 5LIP
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Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
PSEUDOMONAS CEPACIA LIPASE COMPLEXED WITH TRANSITION STATE ANALOGUE OF 1-PHENOXY-2-ACETOXY BUTANE
Overview
In a series of four racemic phenoxyalkyl-alkyl carbinols, 1-phenoxy-2-hydroxybutane (1) is enantioselectively acetylated by Burkholderia cepacia (formerly Pseudomonas cepacia) lipase with an E value > or = 200, whereas for the other three racemates E was found to be < or = 4. To explain the high preference of B. cepacia lipase for (R)-(+)-1, a precursor of its transition state analogue with a tetrahedral P-atom, (R(P),S(P))-O-(2R)-(1-phenoxybut-2-yl)methylphosphonic acid chloride was prepared and crystallized in complex with B. cepacia lipase. The X-ray structure of the complex was determined, allowing to compare the conformation of the inhibitor with results of molecular modelling.
About this Structure
1HQD is a Single protein structure of sequence from Burkholderia cepacia. Full crystallographic information is available from OCA.
Reference
Complex of Burkholderia cepacia lipase with transition state analogue of 1-phenoxy-2-acetoxybutane: biocatalytic, structural and modelling study., Luic M, Tomic S, Lescic I, Ljubovic E, Sepac D, Sunjic V, Vitale L, Saenger W, Kojic-Prodic B, Eur J Biochem. 2001 Jul;268(14):3964-73. PMID:11453990
Page seeded by OCA on Sun Mar 30 21:09:02 2008
Categories: Burkholderia cepacia | Single protein | Triacylglycerol lipase | Kojic-Prodic, B. | Lescic, I. | Ljubovic, E. | Luic, M. | Saenger, W. | Sepac, D. | Sunjic, V. | Tomic, S. | Vitale, L. | Crystal structure | Molecular modelling | Pseudomonas cepacia lipase | Racemic sec alcohol | Transition state (ts) analogue