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1r6w

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(New page: 200px<br /><applet load="1r6w" size="450" color="white" frame="true" align="right" spinBox="true" caption="1r6w, resolution 1.62&Aring;" /> '''Crystal structure of...)
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[[Image:1r6w.jpg|left|200px]]<br /><applet load="1r6w" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1r6w.jpg|left|200px]]<br /><applet load="1r6w" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1r6w, resolution 1.62&Aring;" />
caption="1r6w, resolution 1.62&Aring;" />
'''Crystal structure of the K133R mutant of o-Succinylbenzoate synthase (OSBS) from Escherichia coli. Complex with SHCHC'''<br />
'''Crystal structure of the K133R mutant of o-Succinylbenzoate synthase (OSBS) from Escherichia coli. Complex with SHCHC'''<br />
==Overview==
==Overview==
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o-Succinylbenzoate synthase (OSBS) from Escherichia coli, a member of the, enolase superfamily, catalyzes an exergonic dehydration reaction in the, menaquinone biosynthetic pathway in which, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) is converted, to 4-(2'-carboxyphenyl)-4-oxobutyrate (o-succinylbenzoate or OSB). Our, previous structural studies of the Mg(2+).OSB complex established that, OSBS is a member of the muconate lactonizing enzyme subgroup of the, superfamily: the essential Mg(2+) is coordinated to carboxylate ligands at, the ends of the third, fourth, and fifth beta-strands of the, (beta/alpha)(7)beta-barrel catalytic domain, and the OSB product is, located between the Lys 133 at the end of the second beta-strand and the, Lys 235 at the end of the sixth beta-strand [Thompson, T. B., Garrett, J., B., Taylor, E. A, Meganathan, R., Gerlt, J. A., and Rayment, I. (2000), Biochemistry 39, 10662-76]. Both Lys 133 and Lys 235 were separately, replaced with Ala, Ser, and Arg residues; all six mutants displayed no, detectable catalytic activity. The structure of the Mg(2+).SHCHC complex, of the K133R mutant has been solved at 1.62 A resolution by molecular, replacement starting from the structure of the Mg(2+).OSB complex. This, establishes the absolute configuration of SHCHC: the C1-carboxylate and, the C6-OH leaving group are in a trans orientation, requiring that the, dehydration proceed via a syn stereochemical course. The side chain of Arg, 133 is pointed out of the active site so that it cannot function as a, general base, whereas in the wild-type enzyme complexed with Mg(2+).OSB, the side chain of Lys 133 is appropriately positioned to function as the, only acid/base catalyst in the syn dehydration. The epsilon-ammonium group, of Lys 235 forms a cation-pi interaction with the cyclohexadienyl moiety, of SHCHC, suggesting that Lys 235 also stabilizes the enediolate anion, intermediate in the syn dehydration via a similar interaction.
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o-Succinylbenzoate synthase (OSBS) from Escherichia coli, a member of the enolase superfamily, catalyzes an exergonic dehydration reaction in the menaquinone biosynthetic pathway in which 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) is converted to 4-(2'-carboxyphenyl)-4-oxobutyrate (o-succinylbenzoate or OSB). Our previous structural studies of the Mg(2+).OSB complex established that OSBS is a member of the muconate lactonizing enzyme subgroup of the superfamily: the essential Mg(2+) is coordinated to carboxylate ligands at the ends of the third, fourth, and fifth beta-strands of the (beta/alpha)(7)beta-barrel catalytic domain, and the OSB product is located between the Lys 133 at the end of the second beta-strand and the Lys 235 at the end of the sixth beta-strand [Thompson, T. B., Garrett, J. B., Taylor, E. A, Meganathan, R., Gerlt, J. A., and Rayment, I. (2000) Biochemistry 39, 10662-76]. Both Lys 133 and Lys 235 were separately replaced with Ala, Ser, and Arg residues; all six mutants displayed no detectable catalytic activity. The structure of the Mg(2+).SHCHC complex of the K133R mutant has been solved at 1.62 A resolution by molecular replacement starting from the structure of the Mg(2+).OSB complex. This establishes the absolute configuration of SHCHC: the C1-carboxylate and the C6-OH leaving group are in a trans orientation, requiring that the dehydration proceed via a syn stereochemical course. The side chain of Arg 133 is pointed out of the active site so that it cannot function as a general base, whereas in the wild-type enzyme complexed with Mg(2+).OSB, the side chain of Lys 133 is appropriately positioned to function as the only acid/base catalyst in the syn dehydration. The epsilon-ammonium group of Lys 235 forms a cation-pi interaction with the cyclohexadienyl moiety of SHCHC, suggesting that Lys 235 also stabilizes the enediolate anion intermediate in the syn dehydration via a similar interaction.
==About this Structure==
==About this Structure==
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1R6W 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 MG and 164 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1R6W OCA].
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1R6W 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=MG:'>MG</scene> and <scene name='pdbligand=164:'>164</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1R6W OCA].
==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Gerlt, J.A.]]
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[[Category: Gerlt, J A.]]
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[[Category: Klenchin, V.A.]]
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[[Category: Klenchin, V A.]]
[[Category: Rayment, I.]]
[[Category: Rayment, I.]]
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[[Category: Ringia, E.A.Taylor.]]
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[[Category: Ringia, E A.Taylor.]]
[[Category: 164]]
[[Category: 164]]
[[Category: MG]]
[[Category: MG]]
[[Category: enolase superfamily; tim barrel; capping alpha+beta domain]]
[[Category: enolase superfamily; tim barrel; capping alpha+beta domain]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 01:19:06 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:47:44 2008''

Revision as of 12:47, 21 February 2008


1r6w, resolution 1.62Å

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Crystal structure of the K133R mutant of o-Succinylbenzoate synthase (OSBS) from Escherichia coli. Complex with SHCHC

Overview

o-Succinylbenzoate synthase (OSBS) from Escherichia coli, a member of the enolase superfamily, catalyzes an exergonic dehydration reaction in the menaquinone biosynthetic pathway in which 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) is converted to 4-(2'-carboxyphenyl)-4-oxobutyrate (o-succinylbenzoate or OSB). Our previous structural studies of the Mg(2+).OSB complex established that OSBS is a member of the muconate lactonizing enzyme subgroup of the superfamily: the essential Mg(2+) is coordinated to carboxylate ligands at the ends of the third, fourth, and fifth beta-strands of the (beta/alpha)(7)beta-barrel catalytic domain, and the OSB product is located between the Lys 133 at the end of the second beta-strand and the Lys 235 at the end of the sixth beta-strand [Thompson, T. B., Garrett, J. B., Taylor, E. A, Meganathan, R., Gerlt, J. A., and Rayment, I. (2000) Biochemistry 39, 10662-76]. Both Lys 133 and Lys 235 were separately replaced with Ala, Ser, and Arg residues; all six mutants displayed no detectable catalytic activity. The structure of the Mg(2+).SHCHC complex of the K133R mutant has been solved at 1.62 A resolution by molecular replacement starting from the structure of the Mg(2+).OSB complex. This establishes the absolute configuration of SHCHC: the C1-carboxylate and the C6-OH leaving group are in a trans orientation, requiring that the dehydration proceed via a syn stereochemical course. The side chain of Arg 133 is pointed out of the active site so that it cannot function as a general base, whereas in the wild-type enzyme complexed with Mg(2+).OSB, the side chain of Lys 133 is appropriately positioned to function as the only acid/base catalyst in the syn dehydration. The epsilon-ammonium group of Lys 235 forms a cation-pi interaction with the cyclohexadienyl moiety of SHCHC, suggesting that Lys 235 also stabilizes the enediolate anion intermediate in the syn dehydration via a similar interaction.

About this Structure

1R6W is a Single protein structure of sequence from Escherichia coli with and as ligands. Full crystallographic information is available from OCA.

Reference

Evolution of enzymatic activity in the enolase superfamily: structural and mutagenic studies of the mechanism of the reaction catalyzed by o-succinylbenzoate synthase from Escherichia coli., Klenchin VA, Taylor Ringia EA, Gerlt JA, Rayment I, Biochemistry. 2003 Dec 16;42(49):14427-33. PMID:14661953

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