2qcj
From Proteopedia
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<StructureSection load='2qcj' size='340' side='right'caption='[[2qcj]], [[Resolution|resolution]] 3.00Å' scene=''> | <StructureSection load='2qcj' size='340' side='right'caption='[[2qcj]], [[Resolution|resolution]] 3.00Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2qcj]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[2qcj]] 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=2QCJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2QCJ FirstGlance]. <br> |
| - | </td></tr> | + | </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=2qcj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2qcj OCA], [https://pdbe.org/2qcj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2qcj RCSB], [https://www.ebi.ac.uk/pdbsum/2qcj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2qcj ProSAT]</span></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=2qcj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2qcj OCA], [https://pdbe.org/2qcj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2qcj RCSB], [https://www.ebi.ac.uk/pdbsum/2qcj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2qcj ProSAT]</span></td></tr> | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/PTN22_HUMAN PTN22_HUMAN] Defects in PTPN22 are a cause of susceptibility to systemic lupus erythematosus (SLE) [MIM:[https://omim.org/entry/152700 152700]. SLE is a chronic, inflammatory and often febrile multisystemic disorder of connective tissue. It affects principally the skin, joints, kidneys and serosal membranes. It is thought to represent a failure of the regulatory mechanisms of the autoimmune system.<ref>PMID:15273934</ref> | |
== Function == | == Function == | ||
| - | + | [https://www.uniprot.org/uniprot/PTN22_HUMAN PTN22_HUMAN] Acts as negative regulator of T-cell receptor (TCR) signaling by direct dephosphorylation of the Src family kinases LCK and FYN, ITAMs of the TCRz/CD3 complex, as well as ZAP70, VAV, VCP and other key signaling molecules. Associates with and probably dephosphorylates CBL. Dephosphorylates LCK at its activating 'Tyr-394' residue. Dephosphorylates ZAP70 at its activating 'Tyr-493' residue. Dephosphorylates the immune system activator SKAP2.<ref>PMID:16461343</ref> <ref>PMID:18056643</ref> <ref>PMID:19167335</ref> <ref>PMID:21719704</ref> | |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | + | [[Category: Sun JP]] | |
| - | [[Category: Sun | + | [[Category: Yu X]] |
| - | [[Category: Yu | + | [[Category: Zhang ZY]] |
| - | [[Category: Zhang | + | |
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Revision as of 09:59, 21 December 2022
Native Structure of Lyp
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Categories: Homo sapiens | Large Structures | Sun JP | Yu X | Zhang ZY

