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New page: left|200px<br /><applet load="2gaz" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gaz, resolution 2.61Å" /> '''Mycobacterial lipogl...
 
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[[Image:2gaz.gif|left|200px]]<br /><applet load="2gaz" size="450" color="white" frame="true" align="right" spinBox="true"
caption="2gaz, resolution 2.61&Aring;" />
'''Mycobacterial lipoglycan presentation by CD1d'''<br />


==Overview==
==Mycobacterial lipoglycan presentation by CD1d==
Mycobacterial phosphatidylinositol tetramannosides (PIM4) are agonists for, a distinct population of invariant human (Valpha24) and mouse (Valpha14), NKT cells, when presented by CD1d. We determined the crystal structure at, 2.6-A resolution of mouse CD1d bound to a synthetic dipalmitoyl-PIM2., Natural PIM2, which differs in its fatty acid composition is a, biosynthetic precursor of PIM4, PIM6, lipomannan, and lipoarabinomannan., The PIM2 headgroup (inositol-dimannoside) is the most complex to date, among all the crystallized CD1d ligands and is remarkably ordered in the, CD1d binding groove. A specific hydrogen-bonding network between PIM2 and, CD1d orients the headgroup in the center of the binding groove and above, the A' pocket. A central cluster of hydrophilic CD1d residues (Asp(153), Thr(156), Ser(76), Arg(79)) interacts with the phosphate, inositol, and, alpha1-alpha6-linked mannose of the headgroup, whereas additional, specificity for the alpha1- and alpha2-linked mannose is conferred by, Thr(159). The additional two mannoses in PIM4, relative to PIM2, are, located at the distal 6' carbon of the alpha1-alpha6-linked mannose and, would project away from the CD1d binding groove for interaction with the, TCR. Compared with other CD1d-sphingolipid structures, PIM2 has an, increased number of polar interactions between its headgroup and CD1, but, reduced specificity for the diacylglycerol backbone. Thus, novel NKT cell, agonists can be designed that focus on substitutions of the headgroup, rather than on reducing lipid chain length, as in OCH and PBS-25, two, potent variants of the highly stimulatory invariant NKT cell agonist, alpha-galactosylceramide.
<StructureSection load='2gaz' size='340' side='right'caption='[[2gaz]], [[Resolution|resolution]] 2.61&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2gaz]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GAZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2GAZ 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]] 2.61&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=XPX:(2R)-3-[(HYDROXY{[(2R,3R,5S,6R)-3,4,5-TRIHYDROXY-2,6-BIS(ALPHA-D-MANNOPYRANOSYLOXY)CYCLOHEXYL]OXY}PHOSPHORYL)OXY]PROPANE-1,2-DIYL+DIHEXADECANOATE'>XPX</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=2gaz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2gaz OCA], [https://pdbe.org/2gaz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2gaz RCSB], [https://www.ebi.ac.uk/pdbsum/2gaz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2gaz ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/CD1D1_MOUSE CD1D1_MOUSE] Antigen-presenting protein that binds self and non-self glycolipids and presents them to T-cell receptors on natural killer T-cells.<ref>PMID:11754812</ref> <ref>PMID:16314439</ref> <ref>PMID:16007091</ref>
== 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/ga/2gaz_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.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=2gaz ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Mycobacterial phosphatidylinositol tetramannosides (PIM4) are agonists for a distinct population of invariant human (Valpha24) and mouse (Valpha14) NKT cells, when presented by CD1d. We determined the crystal structure at 2.6-A resolution of mouse CD1d bound to a synthetic dipalmitoyl-PIM2. Natural PIM2, which differs in its fatty acid composition is a biosynthetic precursor of PIM4, PIM6, lipomannan, and lipoarabinomannan. The PIM2 headgroup (inositol-dimannoside) is the most complex to date among all the crystallized CD1d ligands and is remarkably ordered in the CD1d binding groove. A specific hydrogen-bonding network between PIM2 and CD1d orients the headgroup in the center of the binding groove and above the A' pocket. A central cluster of hydrophilic CD1d residues (Asp(153), Thr(156), Ser(76), Arg(79)) interacts with the phosphate, inositol, and alpha1-alpha6-linked mannose of the headgroup, whereas additional specificity for the alpha1- and alpha2-linked mannose is conferred by Thr(159). The additional two mannoses in PIM4, relative to PIM2, are located at the distal 6' carbon of the alpha1-alpha6-linked mannose and would project away from the CD1d binding groove for interaction with the TCR. Compared with other CD1d-sphingolipid structures, PIM2 has an increased number of polar interactions between its headgroup and CD1, but reduced specificity for the diacylglycerol backbone. Thus, novel NKT cell agonists can be designed that focus on substitutions of the headgroup rather than on reducing lipid chain length, as in OCH and PBS-25, two potent variants of the highly stimulatory invariant NKT cell agonist alpha-galactosylceramide.


==About this Structure==
Structural characterization of mycobacterial phosphatidylinositol mannoside binding to mouse CD1d.,Zajonc DM, Ainge GD, Painter GF, Severn WB, Wilson IA J Immunol. 2006 Oct 1;177(7):4577-83. PMID:16982895<ref>PMID:16982895</ref>
2GAZ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with NAG and XPX as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GAZ OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Structural characterization of mycobacterial phosphatidylinositol mannoside binding to mouse CD1d., Zajonc DM, Ainge GD, Painter GF, Severn WB, Wilson IA, J Immunol. 2006 Oct 1;177(7):4577-83. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16982895 16982895]
</div>
<div class="pdbe-citations 2gaz" style="background-color:#fffaf0;"></div>
 
==See Also==
*[[Beta-2 microglobulin 3D structures|Beta-2 microglobulin 3D structures]]
*[[CD1|CD1]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Zajonc DM]]
[[Category: Zajonc, D.M.]]
[[Category: NAG]]
[[Category: XPX]]
[[Category: cd1]]
[[Category: lipid antigen presentation]]
[[Category: mycobacteria]]
[[Category: nkt cells]]
[[Category: tcr]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 11:05:11 2007''

Latest revision as of 08:03, 30 October 2024

Mycobacterial lipoglycan presentation by CD1d

2gaz, resolution 2.61Å

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