9zzv: Difference between revisions

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'''Unreleased structure'''


The entry 9zzv is ON HOLD
==Human T-cell receptor (TCR) with computationally designed orthogonal interface==
 
<StructureSection load='9zzv' size='340' side='right'caption='[[9zzv]], [[Resolution|resolution]] 2.05&Aring;' scene=''>
Authors: Kinjo, T., Yu, S., Nicely, N.I., Leaver-Fay, A., Kim, W.Y., Kuhlman, B.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9zzv]] 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=9ZZV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9ZZV FirstGlance]. <br>
Description: Human T-cell receptor (TCR) with computationally designed orthogonal interface
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.05&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9zzv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9zzv OCA], [https://pdbe.org/9zzv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9zzv RCSB], [https://www.ebi.ac.uk/pdbsum/9zzv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9zzv ProSAT]</span></td></tr>
[[Category: Kim, W.Y]]
</table>
[[Category: Kuhlman, B]]
== Disease ==
[[Category: Leaver-Fay, A]]
[https://www.uniprot.org/uniprot/TRAC_HUMAN TRAC_HUMAN] TCR-alpha-beta-positive T-cell deficiency. The disease is caused by variants affecting the gene represented in this entry.
[[Category: Nicely, N.I]]
== Function ==
[[Category: Kinjo, T]]
[https://www.uniprot.org/uniprot/TRAC_HUMAN TRAC_HUMAN] Constant region of T cell receptor (TR) alpha chain (PubMed:24600447). Alpha-beta T cell receptors are antigen specific receptors which are essential to the immune response and are present on the cell surface of T lymphocytes. Recognize peptide-major histocompatibility (MH) (pMH) complexes that are displayed by antigen presenting cells (APC), a prerequisite for efficient T cell adaptive immunity against pathogens (PubMed:25493333). Binding of alpha-beta TR to pMH complex initiates TR-CD3 clustering on the cell surface and intracellular activation of LCK that phosphorylates the ITAM motifs of CD3G, CD3D, CD3E and CD247 enabling the recruitment of ZAP70. In turn, ZAP70 phosphorylates LAT, which recruits numerous signaling molecules to form the LAT signalosome. The LAT signalosome propagates signal branching to three major signaling pathways, the calcium, the mitogen-activated protein kinase (MAPK) kinase and the nuclear factor NF-kappa-B (NF-kB) pathways, leading to the mobilization of transcription factors that are critical for gene expression and essential for T cell growth and differentiation (PubMed:23524462). The T cell repertoire is generated in the thymus, by V-(D)-J rearrangement. This repertoire is then shaped by intrathymic selection events to generate a peripheral T cell pool of self-MH restricted, non-autoaggressive T cells. Post-thymic interaction of alpha-beta TR with the pMH complexes shapes TR structural and functional avidity (PubMed:15040585).<ref>PMID:15040585</ref> <ref>PMID:23524462</ref> <ref>PMID:24600447</ref> <ref>PMID:25493333</ref>
[[Category: Yu, S]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Kim WY]]
[[Category: Kinjo T]]
[[Category: Kuhlman B]]
[[Category: Leaver-Fay A]]
[[Category: Nicely NI]]
[[Category: Yu S]]

Latest revision as of 14:53, 10 February 2026

Human T-cell receptor (TCR) with computationally designed orthogonal interface

9zzv, resolution 2.05Å

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