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| | {{STRUCTURE_1ocv| PDB=1ocv | SCENE= }} | | {{STRUCTURE_1ocv| PDB=1ocv | SCENE= }} |
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| - | '''THE F116W MUTANT STRUCTURE OF KETOSTEROID ISOMERASE FROM COMAMONAS TESTOSTERONI'''
| + | ===THE F116W MUTANT STRUCTURE OF KETOSTEROID ISOMERASE FROM COMAMONAS TESTOSTERONI=== |
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| - | ==Overview==
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| - | Two homologous Delta5-3-ketosteroid isomerases from Comamonas testosteroni (TI-WT) and Pseudomonas putida biotype B (PI-WT) exhibit different pH activity profiles. TI-WT loses activity below pH 5.0 due to the protonation of the conserved catalytic base, Asp-38, while PI-WT does not. Based on the structural analysis of PI-WT, the critical catalytic base, Asp-38, was found to form a hydrogen bond with the indole ring NH of Trp-116, which is homologously replaced with Phe-116 in TI-WT. To investigate the role of Trp-116, we prepared the F116W mutant of TI-WT (TI-F116W) and the W116F mutant of PI-WT (PI-W116F) and compared kinetic parameters of those mutants at different pH levels. PI-W116F exhibited significantly decreased catalytic activity at acidic pH like TI-WT, whereas TI-F116W maintained catalytic activity at acidic pH like PI-WT and increased the kcat/Km value by 2.5- to 4.7-fold compared with TI-WT at pH 3.8. The crystal structure of TI-F116W clearly showed that the indole ring NH of Trp-116 could form a hydrogen bond with the carboxyl oxygen of Asp-38 like that of PI-WT. The present results demonstrate that the activities of both PI-WT and TI-F116W at low pH were maintained by a tryptophan, which was able not only to lower the pKa value of the catalytic base but also to increase the substrate affinity. This is one example of the strategy nature can adopt to evolve the diversity of the catalytic function in the enzymes. Our results provide insight into deciphering the molecular evolution of the enzyme and creating novel enzymes by protein engineering.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_12734184}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 12734184 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_12734184}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Delta-5-3-ketosteroid]] | | [[Category: Delta-5-3-ketosteroid]] |
| | [[Category: Ketosteroid isomerase]] | | [[Category: Ketosteroid isomerase]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 03:40:47 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 13:26:02 2008'' |
Revision as of 10:26, 28 July 2008
Template:STRUCTURE 1ocv
THE F116W MUTANT STRUCTURE OF KETOSTEROID ISOMERASE FROM COMAMONAS TESTOSTERONI
Template:ABSTRACT PUBMED 12734184
About this Structure
1OCV is a Single protein structure of sequence from Comamonas testosteroni. Full crystallographic information is available from OCA.
Reference
Origin of the different pH activity profile in two homologous ketosteroid isomerases., Yun YS, Lee TH, Nam GH, Jang DS, Shin S, Oh BH, Choi KY, J Biol Chem. 2003 Jul 25;278(30):28229-36. Epub 2003 May 6. PMID:12734184
Page seeded by OCA on Mon Jul 28 13:26:02 2008
