1oi6

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[[Image:1oi6.gif|left|200px]]<br />
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[[Image:1oi6.gif|left|200px]]<br /><applet load="1oi6" size="450" color="white" frame="true" align="right" spinBox="true"
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<applet load="1oi6" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1oi6, resolution 1.40&Aring;" />
caption="1oi6, resolution 1.40&Aring;" />
'''STRUCTURE DETERMINATION OF THE TMP-COMPLEX OF EVAD'''<br />
'''STRUCTURE DETERMINATION OF THE TMP-COMPLEX OF EVAD'''<br />
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==About this Structure==
==About this Structure==
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1OI6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Amycolatopsis_orientalis Amycolatopsis orientalis] with TMP and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Structure known Active Site: AC1. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OI6 OCA].
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1OI6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Amycolatopsis_orientalis Amycolatopsis orientalis] with TMP and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Gol Binding Site For Chain A'>AC1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OI6 OCA].
==Reference==
==Reference==
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[[Category: vancomycin group antibiotic]]
[[Category: vancomycin group antibiotic]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 16:55:23 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 17:44:52 2007''

Revision as of 15:35, 18 December 2007


1oi6, resolution 1.40Å

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STRUCTURE DETERMINATION OF THE TMP-COMPLEX OF EVAD

Overview

Vancomycin, the last line of defense antibiotic, depends upon the, attachment of the carbohydrate vancosamine to an aglycone skeleton for, antibacterial activity. Vancomycin is a naturally occurring secondary, metabolite that can be produced by bacterial fermentation. To combat, emerging resistance, it has been proposed to genetically engineer bacteria, to produce analogues of vancomycin. This requires a detailed understanding, of the biochemical steps in the synthesis of vancomycin. Here we report, the 1.4 A structure and biochemical characterization of EvaD, an RmlC-like, protein that is required for the C-5' epimerization during synthesis of, dTDP-epivancosamine. EvaD, although clearly belonging to the RmlC class of, enzymes, displays very low activity in the archetypal RmlC reaction, (double epimerization of dTDP-6-deoxy-4-keto-D-glucose at C-3' and C-5')., The high resolution structure of EvaD compared with the structures of, authentic RmlC enzymes indicates that a subtle change in the enzyme active, site repositions a key catalytic Tyr residue. A mutant designed to, re-establish the normal position of the Tyr increases the RmlC-like, activity of EvaD.

About this Structure

1OI6 is a Single protein structure of sequence from Amycolatopsis orientalis with TMP and GOL as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

The position of a key tyrosine in dTDP-4-Keto-6-deoxy-D-glucose-5-epimerase (EvaD) alters the substrate profile for this RmlC-like enzyme., Merkel AB, Major LL, Errey JC, Burkart MD, Field RA, Walsh CT, Naismith JH, J Biol Chem. 2004 Jul 30;279(31):32684-91. Epub 2004 May 24. PMID:15159413

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