9jl0

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Current revision (05:32, 3 July 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9jl0 is ON HOLD until Paper Publication
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==Crystal structure of feline CD8aa homodimer==
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<StructureSection load='9jl0' size='340' side='right'caption='[[9jl0]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
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Authors: Li, Z., Liang, R.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9jl0]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Felis_catus Felis catus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9JL0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9JL0 FirstGlance]. <br>
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Description: Crystal structure of feline CD8aa homodimer
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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]] 2.48&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=9jl0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9jl0 OCA], [https://pdbe.org/9jl0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9jl0 RCSB], [https://www.ebi.ac.uk/pdbsum/9jl0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9jl0 ProSAT]</span></td></tr>
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[[Category: Liang, R]]
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</table>
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[[Category: Li, Z]]
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== Function ==
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[https://www.uniprot.org/uniprot/CD8A_FELCA CD8A_FELCA] Integral membrane glycoprotein that plays an essential role in the immune response and serves multiple functions in responses against both external and internal offenses. In T-cells, functions primarily as a coreceptor for MHC class I molecule:peptide complex. The antigens presented by class I peptides are derived from cytosolic proteins while class II derived from extracellular proteins. Interacts simultaneously with the T-cell receptor (TCR) and the MHC class I proteins presented by antigen presenting cells (APCs). In turn, recruits the Src kinase LCK to the vicinity of the TCR-CD3 complex. LCK then initiates different intracellular signaling pathways by phosphorylating various substrates ultimately leading to lymphokine production, motility, adhesion and activation of cytotoxic T-lymphocytes (CTLs). This mechanism enables CTLs to recognize and eliminate infected cells and tumor cells. In NK-cells, the presence of CD8A homodimers at the cell surface provides a survival mechanism allowing conjugation and lysis of multiple target cells. CD8A homodimer molecules also promote the survival and differentiation of activated lymphocytes into memory CD8 T-cells.[UniProtKB:P01732]
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__TOC__
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</StructureSection>
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[[Category: Felis catus]]
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[[Category: Large Structures]]
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[[Category: Li Z]]
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[[Category: Liang R]]

Current revision

Crystal structure of feline CD8aa homodimer

PDB ID 9jl0

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