4lwd

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{{STRUCTURE_4lwd| PDB=4lwd | SCENE= }}
 
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===Human CARMA1 CARD domain===
 
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{{ABSTRACT_PUBMED_24074955}}
 
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==Disease==
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==Human CARMA1 CARD domain==
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[[http://www.uniprot.org/uniprot/CAR11_HUMAN CAR11_HUMAN]] Persistent polyclonal B-cell lymphocytosis. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
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<StructureSection load='4lwd' size='340' side='right'caption='[[4lwd]], [[Resolution|resolution]] 1.79&Aring;' scene=''>
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== Structural highlights ==
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==Function==
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<table><tr><td colspan='2'>[[4lwd]] is a 1 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=4LWD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4LWD FirstGlance]. <br>
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[[http://www.uniprot.org/uniprot/CAR11_HUMAN CAR11_HUMAN]] Involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner. Activates NF-kappa-B via BCL10 and IKK. Stimulates the phosphorylation of BCL10.
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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]] 1.792&#8491;</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=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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==About this Structure==
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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=4lwd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lwd OCA], [https://pdbe.org/4lwd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4lwd RCSB], [https://www.ebi.ac.uk/pdbsum/4lwd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4lwd ProSAT]</span></td></tr>
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[[4lwd]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LWD OCA].
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</table>
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== Disease ==
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==Reference==
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[https://www.uniprot.org/uniprot/CAR11_HUMAN CAR11_HUMAN] Persistent polyclonal B-cell lymphocytosis. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
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<ref group="xtra">PMID:024074955</ref><references group="xtra"/><references/>
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== Function ==
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[https://www.uniprot.org/uniprot/CAR11_HUMAN CAR11_HUMAN] Involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner. Activates NF-kappa-B via BCL10 and IKK. Stimulates the phosphorylation of BCL10.
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__TOC__
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Wu, H.]]
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[[Category: Large Structures]]
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[[Category: Zheng, C.]]
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[[Category: Wu H]]
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[[Category: Bcl10]]
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[[Category: Zheng C]]
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[[Category: Death domain]]
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[[Category: Signaling protein]]
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Current revision

Human CARMA1 CARD domain

PDB ID 4lwd

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