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1x8t

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(New page: 200px<br /><applet load="1x8t" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x8t, resolution 1.9&Aring;" /> '''EPSPS liganded with t...)
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[[Image:1x8t.gif|left|200px]]<br /><applet load="1x8t" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1x8t.gif|left|200px]]<br /><applet load="1x8t" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1x8t, resolution 1.9&Aring;" />
caption="1x8t, resolution 1.9&Aring;" />
'''EPSPS liganded with the (R)-phosphonate analog of the tetrahedral reaction intermediate'''<br />
'''EPSPS liganded with the (R)-phosphonate analog of the tetrahedral reaction intermediate'''<br />
==Overview==
==Overview==
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The enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) catalyzes, the penultimate step of the shikimate pathway and is the target of the, broad-spectrum herbicide glyphosate. Since the functionality of the, shikimate pathway is vital not only for plants but also for, microorganisms, EPSPS is considered a prospective target for the, development of novel antibiotics. We have kinetically analyzed and, determined the crystal structures of Escherichia coli EPSPS inhibited by, (R)- and (S)-configured phosphonate analogues of the tetrahedral reaction, intermediate. Both diastereomers are competitive inhibitors with respect, to the substrates of the EPSPS reaction, shikimate-3-phosphate (S3P) and, phosphoenolpyruvate (PEP). Remarkably, the (S)-phosphonate (K(iS3P) = 750, nM), whose configuration corresponds to that of the genuine tetrahedral, intermediate, is a much weaker inhibitor than the (R)-phosphonate analogue, (K(iS3P) = 16 nM). The crystal structures of EPSPS liganded with the (S)-, and (R)-phosphonates, at 1.5 and 1.9 A resolution, respectively, revealed, that binding of the (R)-phosphonate induces conformational changes of the, strictly conserved residues Arg124 and Glu341 within the active site. This, appears to give rise to substantial structural alterations in the, amino-terminal globular domain of the enzyme. By contrast, binding of the, (S)-phosphonate renders the enzyme structure unchanged. Thus, EPSPS may, facilitate the tight binding of structurally diverse ligands through, conformational flexibility. Molecular docking calculations did not explain, why the (R)-phosphonate is the better inhibitor. Therefore, we propose, that the structural events during the open-closed transition of EPSPS are, altered as a result of inhibitor action.
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The enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) catalyzes the penultimate step of the shikimate pathway and is the target of the broad-spectrum herbicide glyphosate. Since the functionality of the shikimate pathway is vital not only for plants but also for microorganisms, EPSPS is considered a prospective target for the development of novel antibiotics. We have kinetically analyzed and determined the crystal structures of Escherichia coli EPSPS inhibited by (R)- and (S)-configured phosphonate analogues of the tetrahedral reaction intermediate. Both diastereomers are competitive inhibitors with respect to the substrates of the EPSPS reaction, shikimate-3-phosphate (S3P) and phosphoenolpyruvate (PEP). Remarkably, the (S)-phosphonate (K(iS3P) = 750 nM), whose configuration corresponds to that of the genuine tetrahedral intermediate, is a much weaker inhibitor than the (R)-phosphonate analogue (K(iS3P) = 16 nM). The crystal structures of EPSPS liganded with the (S)- and (R)-phosphonates, at 1.5 and 1.9 A resolution, respectively, revealed that binding of the (R)-phosphonate induces conformational changes of the strictly conserved residues Arg124 and Glu341 within the active site. This appears to give rise to substantial structural alterations in the amino-terminal globular domain of the enzyme. By contrast, binding of the (S)-phosphonate renders the enzyme structure unchanged. Thus, EPSPS may facilitate the tight binding of structurally diverse ligands through conformational flexibility. Molecular docking calculations did not explain why the (R)-phosphonate is the better inhibitor. Therefore, we propose that the structural events during the open-closed transition of EPSPS are altered as a result of inhibitor action.
==About this Structure==
==About this Structure==
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1X8T 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 RC1 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=1X8T OCA].
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1X8T 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=RC1:'>RC1</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=1X8T OCA].
==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Alberg, D.G.]]
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[[Category: Alberg, D G.]]
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[[Category: Bartlett, P.A.]]
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[[Category: Bartlett, P A.]]
[[Category: Becker, A.]]
[[Category: Becker, A.]]
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[[Category: Healy, M.L.]]
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[[Category: Healy, M L.]]
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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 Wed Nov 21 05:54:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:52:11 2008''

Revision as of 13:52, 21 February 2008


1x8t, resolution 1.9Å

Drag the structure with the mouse to rotate

EPSPS liganded with the (R)-phosphonate analog of the tetrahedral reaction intermediate

Overview

The enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) catalyzes the penultimate step of the shikimate pathway and is the target of the broad-spectrum herbicide glyphosate. Since the functionality of the shikimate pathway is vital not only for plants but also for microorganisms, EPSPS is considered a prospective target for the development of novel antibiotics. We have kinetically analyzed and determined the crystal structures of Escherichia coli EPSPS inhibited by (R)- and (S)-configured phosphonate analogues of the tetrahedral reaction intermediate. Both diastereomers are competitive inhibitors with respect to the substrates of the EPSPS reaction, shikimate-3-phosphate (S3P) and phosphoenolpyruvate (PEP). Remarkably, the (S)-phosphonate (K(iS3P) = 750 nM), whose configuration corresponds to that of the genuine tetrahedral intermediate, is a much weaker inhibitor than the (R)-phosphonate analogue (K(iS3P) = 16 nM). The crystal structures of EPSPS liganded with the (S)- and (R)-phosphonates, at 1.5 and 1.9 A resolution, respectively, revealed that binding of the (R)-phosphonate induces conformational changes of the strictly conserved residues Arg124 and Glu341 within the active site. This appears to give rise to substantial structural alterations in the amino-terminal globular domain of the enzyme. By contrast, binding of the (S)-phosphonate renders the enzyme structure unchanged. Thus, EPSPS may facilitate the tight binding of structurally diverse ligands through conformational flexibility. Molecular docking calculations did not explain why the (R)-phosphonate is the better inhibitor. Therefore, we propose that the structural events during the open-closed transition of EPSPS are altered as a result of inhibitor action.

About this Structure

1X8T 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

Interaction of phosphonate analogues of the tetrahedral reaction intermediate with 5-enolpyruvylshikimate-3-phosphate synthase in atomic detail., Priestman MA, Healy ML, Becker A, Alberg DG, Bartlett PA, Lushington GH, Schonbrunn E, Biochemistry. 2005 Mar 8;44(9):3241-8. PMID:15736934

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