1xdd

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[[Image:1xdd.gif|left|200px]]
[[Image:1xdd.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1xdd |SIZE=350|CAPTION= <scene name='initialview01'>1xdd</scene>, resolution 2.20&Aring;
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The line below this paragraph, containing "STRUCTURE_1xdd", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=AAY:8-[2-((2S)-4-HYDROXY-1-{[5-(HYDROXYMETHYL)-6-METHOXY-2-NAPHTHYL]METHYL}-6-OXOPIPERIDIN-2-YL)ETHYL]-3,7-DIMETHYL-1,2,3,7,8,8A-HEXAHYDRONAPHTHALEN-1-YL+2-METHYLBUTANOATE'>AAY</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1xdd| PDB=1xdd | SCENE= }}
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|RELATEDENTRY=[[1xdg|1XDG]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1xdd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1xdd OCA], [http://www.ebi.ac.uk/pdbsum/1xdd PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1xdd RCSB]</span>
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}}
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'''X-ray structure of LFA-1 I-domain in complex with LFA703 at 2.2A resolution'''
'''X-ray structure of LFA-1 I-domain in complex with LFA703 at 2.2A resolution'''
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[[Category: Weitz-Schmidt, G.]]
[[Category: Weitz-Schmidt, G.]]
[[Category: Welzenbach, K.]]
[[Category: Welzenbach, K.]]
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[[Category: i-domain]]
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[[Category: I-domain]]
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[[Category: rossman fold]]
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[[Category: Rossman fold]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:53:12 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:48:03 2008''
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Revision as of 11:53, 3 May 2008

Template:STRUCTURE 1xdd

X-ray structure of LFA-1 I-domain in complex with LFA703 at 2.2A resolution


Overview

The integrin lymphocyte function-associated antigen-1 (LFA-1) (alphaLbeta2; CD11a/CD18) plays an important role in leukocyte migration and T cell activation. LFA-1 is inhibited by the cholesterol-lowering drug lovastatin, which binds to an allosteric site of the alphaL I domain termed the lovastatin site (L-site). Here we report for the first time the x-ray structures of the LFA-1 I domain complexed with derivatives of lovastatin optimized for LFA-1 inhibition. This analysis identified two new subpockets within the L-site occupied by chemical groups of the statin derivatives but not by lovastatin itself. Occupancy of these L-site subpockets led to distinct conformational changes in LFA-1, which were detectable by an epitope-monitoring assay. We utilized this assay to demonstrate improved LFA-1 inhibition in human blood in vitro and in blood samples from treated animals ex vivo. Moreover, we demonstrate that the novel lovastatin-derived LFA-1 inhibitor LFA878 exhibits potent anti-inflammatory effects in carrageenan-induced rat paw edema. In summary, the findings reported here extend the understanding of LFA-1 inhibition at the molecular level, allow for the identification and design of LFA-1 inhibitors of further enhanced potency, and support the expectation that LFA-1 inhibitors binding to the L-site will be of therapeutic value in treating inflammatory diseases.

About this Structure

1XDD is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Improved lymphocyte function-associated antigen-1 (LFA-1) inhibition by statin derivatives: molecular basis determined by x-ray analysis and monitoring of LFA-1 conformational changes in vitro and ex vivo., Weitz-Schmidt G, Welzenbach K, Dawson J, Kallen J, J Biol Chem. 2004 Nov 5;279(45):46764-71. Epub 2004 Aug 10. PMID:15304496 Page seeded by OCA on Sat May 3 14:53:12 2008

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