1xdd: Difference between revisions

New page: left|200px<br /> <applet load="1xdd" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xdd, resolution 2.20Å" /> '''X-ray structure of ...
 
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[[Image:1xdd.gif|left|200px]]<br />
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'''X-ray structure of LFA-1 I-domain in complex with LFA703 at 2.2A resolution'''<br />


==Overview==
==X-ray structure of LFA-1 I-domain in complex with LFA703 at 2.2A resolution==
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.
<StructureSection load='1xdd' size='340' side='right'caption='[[1xdd]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1xdd]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XDD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1XDD FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><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></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1xdd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1xdd OCA], [https://pdbe.org/1xdd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1xdd RCSB], [https://www.ebi.ac.uk/pdbsum/1xdd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1xdd ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/ITAL_HUMAN ITAL_HUMAN] Integrin alpha-L/beta-2 is a receptor for ICAM1, ICAM2, ICAM3 and ICAM4. It is involved in a variety of immune phenomena including leukocyte-endothelial cell interaction, cytotoxic T-cell mediated killing, and antibody dependent killing by granulocytes and monocytes.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/xd/1xdd_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1xdd ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
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==
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<ref>PMID:15304496</ref>
1XDD is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MG and AAY as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1XDD OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15304496 15304496]
</div>
<div class="pdbe-citations 1xdd" style="background-color:#fffaf0;"></div>
 
==See Also==
*[[Integrin 3D structures|Integrin 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Large Structures]]
[[Category: Dawson, J.]]
[[Category: Dawson J]]
[[Category: Kallen, J.]]
[[Category: Kallen J]]
[[Category: Weitz-Schmidt, G.]]
[[Category: Weitz-Schmidt G]]
[[Category: Welzenbach, K.]]
[[Category: Welzenbach K]]
[[Category: AAY]]
[[Category: MG]]
[[Category: i-domain]]
[[Category: rossman fold]]
 
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