1fui

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Revision as of 16:10, 20 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1fui" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fui, resolution 2.50Å" /> '''L-FUCOSE ISOMERASE F...)
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File:1fui.gif


1fui, resolution 2.50Å

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L-FUCOSE ISOMERASE FROM ESCHERICHIA COLI

OverviewOverview

The three-dimensional structure of L-fucose isomerase from Escherichia, coli has been determined by X-ray crystallography at 2.5 A resolution., This ketol isomerase converts the aldose L-fucose into the corresponding, ketose L-fuculose using Mn2+ as a cofactor. Being a hexamer with 64,976 Da, per subunit, L-fucose isomerase is the largest structurally known ketol, isomerase. The enzyme shows neither sequence nor structural similarity, with other ketol isomerases. The hexamer obeys D3 symmetry and forms the, crystallographic asymmetric unit. The strict and favorably oriented local, symmetry allowed for a computational phase extension from 7.3 A to 2.5 A, resolution. The structure was solved with an L-fucitol molecule bound to, the catalytic center such that the hydroxyl groups at positions 1 and 2, are ligands of the manganese ion. Most likely, L-fucitol mimics a bound, L-fucose molecule in its open chain form. The protein environment suggests, strongly that the reaction belongs to the ene-diol type.

About this StructureAbout this Structure

1FUI is a Single protein structure of sequence from Escherichia coli with MN, SO4 and FOC as ligands. Active as Arabinose isomerase, with EC number 5.3.1.3 Full crystallographic information is available from OCA.

ReferenceReference

Structure and mechanism of L-fucose isomerase from Escherichia coli., Seemann JE, Schulz GE, J Mol Biol. 1997 Oct 17;273(1):256-68. PMID:9367760

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