1klf

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(New page: 200px<br /><applet load="1klf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1klf, resolution 2.79&Aring;" /> '''FIMH ADHESIN-FIMC CH...)
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Revision as of 17:13, 20 November 2007


1klf, resolution 2.79Å

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FIMH ADHESIN-FIMC CHAPERONE COMPLEX WITH D-MANNOSE

Overview

The first step in the colonization of the human urinary tract by, pathogenic Escherichia coli is the mannose-sensitive binding of FimH, the, adhesin present at the tip of type 1 pili, to the bladder epithelium. We, elucidated crystallographically the interactions of FimH with D-mannose., The unique site binding pocket occupied by D-mannose was probed using, site-directed mutagenesis. All but one of the mutants examined had greatly, diminished mannose-binding activity and had also lost the ability to bind, human bladder cells. The binding activity of the mono-saccharide D-mannose, was delineated from this of mannotriose (Man(alpha 1-3)[Man(alpha, 1-6)]Man) by generating mutants that abolished D-mannose binding but, retained mannotriose binding activity. Our structure/function analysis, demonstrated that the binding of the monosaccharide alpha-D-mannose is the, primary bladder cell receptor for uropathogenic E. coli and that this, event requires a highly conserved FimH binding pocket. The residues in the, FimH mannose-binding pocket were sequenced and found to be invariant in, over 200 uropathogenic strains of E. coli. Only enterohaemorrhagic E. coli, (EHEC) possess a sequence variation within the mannose-binding pocket of, FimH, suggesting a naturally occurring mechanism of attenuation in EHEC, bacteria that would prevent them from being targeted to the urinary tract.

About this Structure

1KLF is a Protein complex structure of sequences from Escherichia coli with MAN as ligand. Full crystallographic information is available from OCA.

Reference

Structural basis of tropism of Escherichia coli to the bladder during urinary tract infection., Hung CS, Bouckaert J, Hung D, Pinkner J, Widberg C, DeFusco A, Auguste CG, Strouse R, Langermann S, Waksman G, Hultgren SJ, Mol Microbiol. 2002 May;44(4):903-15. PMID:12010488

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