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5mgr

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==Human receptor NKR-P1 in glycosylated form, extracellular domain==
==Human receptor NKR-P1 in glycosylated form, extracellular domain==
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<StructureSection load='5mgr' size='340' side='right' caption='[[5mgr]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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<StructureSection load='5mgr' size='340' side='right'caption='[[5mgr]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[5mgr]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5MGR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5MGR FirstGlance]. <br>
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<table><tr><td colspan='2'>[[5mgr]] 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=5MGR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5MGR FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><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></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5mgr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5mgr OCA], [http://pdbe.org/5mgr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5mgr RCSB], [http://www.ebi.ac.uk/pdbsum/5mgr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5mgr ProSAT]</span></td></tr>
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<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></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5mgr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5mgr OCA], [https://pdbe.org/5mgr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5mgr RCSB], [https://www.ebi.ac.uk/pdbsum/5mgr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5mgr ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
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[[http://www.uniprot.org/uniprot/KLRB1_HUMAN KLRB1_HUMAN]] Plays an inhibitory role on natural killer (NK) cells cytotoxicity. Activation results in specific acid sphingomyelinase/SMPD1 stimulation with subsequent marked elevation of intracellular ceramide. Activation also leads to AKT1/PKB and RPS6KA1/RSK1 kinases stimulation as well as markedly enhanced T-cell proliferation induced by anti-CD3. Acts as a lectin that binds to the terminal carbohydrate Gal-alpha(1,3)Gal epitope as well as to the N-acetyllactosamine epitope. Binds also to CLEC2D/LLT1 as a ligand and inhibits NK cell-mediated cytotoxicity as well as interferon-gamma secretion in target cells.<ref>PMID:16455998</ref> <ref>PMID:16925668</ref> <ref>PMID:8077657</ref>
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[https://www.uniprot.org/uniprot/KLRB1_HUMAN KLRB1_HUMAN] Plays an inhibitory role on natural killer (NK) cells cytotoxicity. Activation results in specific acid sphingomyelinase/SMPD1 stimulation with subsequent marked elevation of intracellular ceramide. Activation also leads to AKT1/PKB and RPS6KA1/RSK1 kinases stimulation as well as markedly enhanced T-cell proliferation induced by anti-CD3. Acts as a lectin that binds to the terminal carbohydrate Gal-alpha(1,3)Gal epitope as well as to the N-acetyllactosamine epitope. Binds also to CLEC2D/LLT1 as a ligand and inhibits NK cell-mediated cytotoxicity as well as interferon-gamma secretion in target cells.<ref>PMID:16455998</ref> <ref>PMID:16925668</ref> <ref>PMID:8077657</ref>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Blaha, J]]
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[[Category: Homo sapiens]]
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[[Category: Dohnalek, J]]
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[[Category: Large Structures]]
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[[Category: Harlos, K]]
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[[Category: Blaha J]]
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[[Category: Hasek, J]]
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[[Category: Dohnalek J]]
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[[Category: Koval, T]]
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[[Category: Harlos K]]
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[[Category: Skalova, T]]
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[[Category: Hasek J]]
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[[Category: Stransky, J]]
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[[Category: Koval T]]
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[[Category: Vanek, O]]
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[[Category: Skalova T]]
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[[Category: Yuguang, Z]]
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[[Category: Stransky J]]
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[[Category: Ctl fold]]
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[[Category: Vanek O]]
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[[Category: Immune system]]
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[[Category: Yuguang Z]]
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[[Category: Natural killer cell]]
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[[Category: Receptor]]
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Current revision

Human receptor NKR-P1 in glycosylated form, extracellular domain

PDB ID 5mgr

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