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New page: left|200px<br /><applet load="1a2n" size="450" color="white" frame="true" align="right" spinBox="true" caption="1a2n, resolution 2.8Å" /> '''STRUCTURE OF THE C115...
 
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[[Image:1a2n.jpg|left|200px]]<br /><applet load="1a2n" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1a2n.jpg|left|200px]]<br /><applet load="1a2n" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1a2n, resolution 2.8&Aring;" />
caption="1a2n, resolution 2.8&Aring;" />
'''STRUCTURE OF THE C115A MUTANT OF MURA COMPLEXED WITH THE FLUORINATED ANALOG OF THE REACTION TETRAHEDRAL INTERMEDIATE'''<br />
'''STRUCTURE OF THE C115A MUTANT OF MURA COMPLEXED WITH THE FLUORINATED ANALOG OF THE REACTION TETRAHEDRAL INTERMEDIATE'''<br />


==Overview==
==Overview==
MurA (UDP-GlcNAc enolpyruvyl transferase), the first enzyme in bacterial, peptidoglycan biosynthesis, catalyzes the enolpyruvyl transfer from, phosphoenolpyruvate (PEP) to the 3'-OH of UDP-GlcNAc by an, addition-elimination mechanism that proceeds through a tetrahedral ketal, intermediate. The crystal structure of the Cys115-to-Ala (C115A) mutant of, Escherichia coli MurA complexed with a fluoro analogue of the tetrahedral, intermediate revealed the absolute configuration of the adduct and the, stereochemical course of the reaction. The fluorinated adduct was, generated in a preincubation of wild-type MurA with, (Z)-3-fluorophosphoenolpyruvate (FPEP) and UDP-GlcNAc and purified after, enzyme denaturation. The fluorine substituent stabilizes the tetrahedral, intermediate toward decomposition by a factor of 10(4)-10(6), facilitating, manipulation of the adduct. The C115A mutant of MurA was utilized to avoid, the microheterogeneity that arises in the wild-type MurA from the attack, of Cys115 on C-2 of FPEP in competition with the formation of the, fluorinated adduct. The crystal structure of the complex was determined to, 2.8 A resolution, and the absolute configuration at C-2 of the adduct was, found to be 2R. Thus, addition of the 3'-OH of UDP-GlcNAc is to the 2-si, face of FPEP, corresponding to the 2-re face of PEP. Given the previous, observation that, in D2O, the addition of D+ to C-3 of PEP proceeds from, the 2-si face [Kim, D. H., Lees, W. J., and Walsh, C. T. (1995) J. Am., Chem. Soc. 117, 6380-6381], the addition across the double bond of PEP is, anti. Also, because the overall stereochemical course has been shown to be, either anti/syn or syn/anti [Lees, W. J., and Walsh, C. T. (1995) J. Am., Chem. Soc. 117, 7329-7337], it now follows that the stereochemistry of, elimination of H+ from C-3 and Pi from C-2 of the tetrahedral intermediate, of the reaction is syn.
MurA (UDP-GlcNAc enolpyruvyl transferase), the first enzyme in bacterial peptidoglycan biosynthesis, catalyzes the enolpyruvyl transfer from phosphoenolpyruvate (PEP) to the 3'-OH of UDP-GlcNAc by an addition-elimination mechanism that proceeds through a tetrahedral ketal intermediate. The crystal structure of the Cys115-to-Ala (C115A) mutant of Escherichia coli MurA complexed with a fluoro analogue of the tetrahedral intermediate revealed the absolute configuration of the adduct and the stereochemical course of the reaction. The fluorinated adduct was generated in a preincubation of wild-type MurA with (Z)-3-fluorophosphoenolpyruvate (FPEP) and UDP-GlcNAc and purified after enzyme denaturation. The fluorine substituent stabilizes the tetrahedral intermediate toward decomposition by a factor of 10(4)-10(6), facilitating manipulation of the adduct. The C115A mutant of MurA was utilized to avoid the microheterogeneity that arises in the wild-type MurA from the attack of Cys115 on C-2 of FPEP in competition with the formation of the fluorinated adduct. The crystal structure of the complex was determined to 2.8 A resolution, and the absolute configuration at C-2 of the adduct was found to be 2R. Thus, addition of the 3'-OH of UDP-GlcNAc is to the 2-si face of FPEP, corresponding to the 2-re face of PEP. Given the previous observation that, in D2O, the addition of D+ to C-3 of PEP proceeds from the 2-si face [Kim, D. H., Lees, W. J., and Walsh, C. T. (1995) J. Am. Chem. Soc. 117, 6380-6381], the addition across the double bond of PEP is anti. Also, because the overall stereochemical course has been shown to be either anti/syn or syn/anti [Lees, W. J., and Walsh, C. T. (1995) J. Am. Chem. Soc. 117, 7329-7337], it now follows that the stereochemistry of elimination of H+ from C-3 and Pi from C-2 of the tetrahedral intermediate of the reaction is syn.


==About this Structure==
==About this Structure==
1A2N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with TET as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/UDP-N-acetylglucosamine_1-carboxyvinyltransferase UDP-N-acetylglucosamine 1-carboxyvinyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.7 2.5.1.7] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1A2N OCA].  
1A2N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=TET:'>TET</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/UDP-N-acetylglucosamine_1-carboxyvinyltransferase UDP-N-acetylglucosamine 1-carboxyvinyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.7 2.5.1.7] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A2N OCA].  


==Reference==
==Reference==
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[[Category: udp-n-acetylglucosamine]]
[[Category: udp-n-acetylglucosamine]]


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