22dy: Difference between revisions
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New page: '''Unreleased structure''' The entry 22dy is ON HOLD Authors: Wang, Y.J., Sun, L. Description: Local structure of MERS-CoV S protein bound with receptor DPP4 in the conformation 2 (2 u... |
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==Local structure of MERS-CoV S protein bound with receptor DPP4 in the conformation 2 (2 up RBD and 2 DPP4 bound)== | |||
<StructureSection load='22dy' size='340' side='right'caption='[[22dy]], [[Resolution|resolution]] 3.35Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[22dy]] is a 7 chain structure with sequence from [https://en.wikipedia.org/wiki/Betacoronavirus_England_1 Betacoronavirus England 1] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=22DY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=22DY FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.35Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=22dy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=22dy OCA], [https://pdbe.org/22dy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=22dy RCSB], [https://www.ebi.ac.uk/pdbsum/22dy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=22dy ProSAT]</span></td></tr> | ||
[[Category: | </table> | ||
[[Category: Sun | == Function == | ||
[https://www.uniprot.org/uniprot/DPP4_HUMAN DPP4_HUMAN] Cell surface glycoprotein receptor involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Acts as a positive regulator of T-cell coactivation, by binding at least ADA, CAV1, IGF2R, and PTPRC. Its binding to CAV1 and CARD11 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner. Its interaction with ADA also regulates lymphocyte-epithelial cell adhesion. In association with FAP is involved in the pericellular proteolysis of the extracellular matrix (ECM), the migration and invasion of endothelial cells into the ECM. May be involved in the promotion of lymphatic endothelial cells adhesion, migration and tube formation. When overexpressed, enhanced cell proliferation, a process inhibited by GPC3. Acts also as a serine exopeptidase with a dipeptidyl peptidase activity that regulates various physiological processes by cleaving peptides in the circulation, including many chemokines, mitogenic growth factors, neuropeptides and peptide hormones. Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline.<ref>PMID:10951221</ref> <ref>PMID:17549790</ref> <ref>PMID:10570924</ref> <ref>PMID:10900005</ref> <ref>PMID:11772392</ref> <ref>PMID:14691230</ref> <ref>PMID:16651416</ref> <ref>PMID:17287217</ref> <ref>PMID:18708048</ref> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Betacoronavirus England 1]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Sun L]] | |||
[[Category: Wang YJ]] | |||
Latest revision as of 16:38, 8 September 2026
Local structure of MERS-CoV S protein bound with receptor DPP4 in the conformation 2 (2 up RBD and 2 DPP4 bound)
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