1oax

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Revision as of 20:49, 29 October 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1oax" size="450" color="white" frame="true" align="right" spinBox="true" caption="1oax, resolution 2.67Å" /> '''FV STRUCTURE OF THE...)
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File:1oax.gif


1oax, resolution 2.67Å

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FV STRUCTURE OF THE IGE SPE-7 IN COMPLEX WITH ACENAPHTHENEQUINONE

OverviewOverview

A single antibody was shown to adopt different binding-site conformations, and thereby bind unrelated antigens. Analysis by both x-ray, crystallography and pre-steady-state kinetics revealed an equilibrium, between different preexisting isomers, one of which possessed a, promiscuous, low-affinity binding site for aromatic ligands, including the, immunizing hapten. A subsequent induced-fit isomerization led to, high-affinity complexes with a deep and narrow binding site. A protein, antigen identified by repertoire selection made use of an unrelated, antibody isomer with a wide, shallow binding site. Conformational, diversity, whereby one sequence adopts multiple structures and multiple, functions, can increase the effective size of the antibody repertoire but, may also lead to autoimmunity ... [(full description)]

About this StructureAbout this Structure

1OAX is a [Protein complex] structure of sequences from [Rattus rattus] with ANQ as [ligand]. Full crystallographic information is available from [OCA].

ReferenceReference

Antibody multispecificity mediated by conformational diversity., James LC, Roversi P, Tawfik DS, Science. 2003 Feb 28;299(5611):1362-7. PMID:12610298

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