1xlm

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Revision as of 21:25, 29 October 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1xlm" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xlm, resolution 2.4Å" /> '''D254E, D256E MUTANT ...)
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File:1xlm.gif


1xlm, resolution 2.4Å

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D254E, D256E MUTANT OF D-XYLOSE ISOMERASE COMPLEXED WITH AL3 AND XYLITOL

OverviewOverview

The active site and mechanism of D-xylose isomerase have been probed by, determination of the crystal structures of the enzyme bound to various, substrates, inhibitors and cations. Ring-opening is an obligatory first, step of the reaction and is believed to be the rate-determining step for, the aldose to ketose conversion. The structure of a complex with a cyclic, thio-glucose has been determined and it is concluded that this is an, analogue of the Michaelis complex. At -10 degrees C substrates in crystals, are observed in the extended chain form. The absence of an appropriately, situated base for either the cyclic or extended chain forms from the, substrate binding site indicates that the isomerisation does not take, place by an enediol or enediolate mechanism. Binding of a trivalent ... [(full description)]

About this StructureAbout this Structure

1XLM is a [Single protein] structure of sequence from [Arthrobacter sp.] with XYL and AL as [ligands]. Active as [[1]], with EC number [5.3.1.5]. Full crystallographic information is available from [OCA].

ReferenceReference

Mechanism for aldose-ketose interconversion by D-xylose isomerase involving ring opening followed by a 1,2-hydride shift., Collyer CA, Henrick K, Blow DM, J Mol Biol. 1990 Mar 5;212(1):211-35. PMID:2319597

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