1mi4

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(New page: 200px<br /><applet load="1mi4" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mi4, resolution 1.7&Aring;" /> '''Glyphosate insensitiv...)
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[[Image:1mi4.gif|left|200px]]<br /><applet load="1mi4" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1mi4, resolution 1.7&Aring;" />
caption="1mi4, resolution 1.7&Aring;" />
'''Glyphosate insensitive G96A mutant EPSP synthase liganded with shikimate-3-phosphate'''<br />
'''Glyphosate insensitive G96A mutant EPSP synthase liganded with shikimate-3-phosphate'''<br />
==Overview==
==Overview==
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The enzyme 5-enolpyruvyl shikimate-3-phosphate (EPSP) synthase (EC, 2.5.1.19) is essential for the biosynthesis of aromatic compounds in, plants and microbes and is the unique target of the herbicide glyphosate., One of the first glyphosate-insensitive enzymes reported was a Gly96Ala, mutant of EPSP synthase from Klebsiella pneumoniae. We have introduced, this single-site mutation into the highly homologous EPSP synthase from, Escherichia coli. The mutant enzyme is insensitive to glyphosate with, unaltered affinity for its first substrate, shikimate-3-phosphate (S3P), but displays a 30-fold lower affinity for its second substrate, phosphoenolpyruvate (PEP). Using X-ray crystallography, we solved the, structure of Gly96Ala-EPSP synthase liganded with S3P to 0.17 nm, resolution. The crystal structure shows that the additional methyl group, from Ala96 protrudes into the active site of the enzyme. While the, interactions between enzyme and S3P remain unaffected, the accessible, volume for glyphosate binding is substantially reduced. Exploiting the, crystallographic results for molecular modeling, we demonstrate that PEP, but not glyphosate can be docked in the Gly96Ala-modified binding site., The predicted PEP binding site satisfies the earlier proposed interaction, pattern for PEP with EPSP synthase and corroborates the assumption that, glyphosate and PEP target the same binding site.
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The enzyme 5-enolpyruvyl shikimate-3-phosphate (EPSP) synthase (EC 2.5.1.19) is essential for the biosynthesis of aromatic compounds in plants and microbes and is the unique target of the herbicide glyphosate. One of the first glyphosate-insensitive enzymes reported was a Gly96Ala mutant of EPSP synthase from Klebsiella pneumoniae. We have introduced this single-site mutation into the highly homologous EPSP synthase from Escherichia coli. The mutant enzyme is insensitive to glyphosate with unaltered affinity for its first substrate, shikimate-3-phosphate (S3P), but displays a 30-fold lower affinity for its second substrate, phosphoenolpyruvate (PEP). Using X-ray crystallography, we solved the structure of Gly96Ala-EPSP synthase liganded with S3P to 0.17 nm resolution. The crystal structure shows that the additional methyl group from Ala96 protrudes into the active site of the enzyme. While the interactions between enzyme and S3P remain unaffected, the accessible volume for glyphosate binding is substantially reduced. Exploiting the crystallographic results for molecular modeling, we demonstrate that PEP but not glyphosate can be docked in the Gly96Ala-modified binding site. The predicted PEP binding site satisfies the earlier proposed interaction pattern for PEP with EPSP synthase and corroborates the assumption that glyphosate and PEP target the same binding site.
==About this Structure==
==About this Structure==
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1MI4 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 S3P and FMT as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/3-phosphoshikimate_1-carboxyvinyltransferase 3-phosphoshikimate 1-carboxyvinyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.19 2.5.1.19] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MI4 OCA].
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1MI4 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=S3P:'>S3P</scene> and <scene name='pdbligand=FMT:'>FMT</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/3-phosphoshikimate_1-carboxyvinyltransferase 3-phosphoshikimate 1-carboxyvinyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.19 2.5.1.19] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MI4 OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Eschenburg, S.]]
[[Category: Eschenburg, S.]]
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[[Category: Healy, M.L.]]
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[[Category: Healy, M L.]]
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[[Category: Lushington, G.H.]]
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[[Category: Lushington, G H.]]
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[[Category: Priestman, M.A.]]
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[[Category: Priestman, M A.]]
[[Category: Schonbrunn, E.]]
[[Category: Schonbrunn, E.]]
[[Category: FMT]]
[[Category: FMT]]
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[[Category: inside-out alpha-beta barrel]]
[[Category: inside-out alpha-beta barrel]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 21:25:49 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:55:23 2008''

Revision as of 11:55, 21 February 2008


1mi4, resolution 1.7Å

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Glyphosate insensitive G96A mutant EPSP synthase liganded with shikimate-3-phosphate

Overview

The enzyme 5-enolpyruvyl shikimate-3-phosphate (EPSP) synthase (EC 2.5.1.19) is essential for the biosynthesis of aromatic compounds in plants and microbes and is the unique target of the herbicide glyphosate. One of the first glyphosate-insensitive enzymes reported was a Gly96Ala mutant of EPSP synthase from Klebsiella pneumoniae. We have introduced this single-site mutation into the highly homologous EPSP synthase from Escherichia coli. The mutant enzyme is insensitive to glyphosate with unaltered affinity for its first substrate, shikimate-3-phosphate (S3P), but displays a 30-fold lower affinity for its second substrate, phosphoenolpyruvate (PEP). Using X-ray crystallography, we solved the structure of Gly96Ala-EPSP synthase liganded with S3P to 0.17 nm resolution. The crystal structure shows that the additional methyl group from Ala96 protrudes into the active site of the enzyme. While the interactions between enzyme and S3P remain unaffected, the accessible volume for glyphosate binding is substantially reduced. Exploiting the crystallographic results for molecular modeling, we demonstrate that PEP but not glyphosate can be docked in the Gly96Ala-modified binding site. The predicted PEP binding site satisfies the earlier proposed interaction pattern for PEP with EPSP synthase and corroborates the assumption that glyphosate and PEP target the same binding site.

About this Structure

1MI4 is a Single protein structure of sequence from Escherichia coli with and as ligands. Active as 3-phosphoshikimate 1-carboxyvinyltransferase, with EC number 2.5.1.19 Full crystallographic information is available from OCA.

Reference

How the mutation glycine96 to alanine confers glyphosate insensitivity to 5-enolpyruvyl shikimate-3-phosphate synthase from Escherichia coli., Eschenburg S, Healy ML, Priestman MA, Lushington GH, Schonbrunn E, Planta. 2002 Nov;216(1):129-35. Epub 2002 Nov 12. PMID:12430021

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