7x8t: Difference between revisions

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'''Unreleased structure'''


The entry 7x8t is ON HOLD
==Frizzled 10 CRD in complex with hB9L9.3 Fab==
<StructureSection load='7x8t' size='340' side='right'caption='[[7x8t]], [[Resolution|resolution]] 2.51&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[7x8t]] is a 12 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=7X8T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7X8T FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.51&#8491;</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=7x8t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7x8t OCA], [https://pdbe.org/7x8t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7x8t RCSB], [https://www.ebi.ac.uk/pdbsum/7x8t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7x8t ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/FZD10_HUMAN FZD10_HUMAN] Receptor for Wnt proteins. Functions in the canonical Wnt/beta-catenin signaling pathway (By similarity). The canonical Wnt/beta-catenin signaling pathway leads to the activation of disheveled proteins, inhibition of GSK-3 kinase, nuclear accumulation of beta-catenin and activation of Wnt target genes. A second signaling pathway involving PKC and calcium fluxes has been seen for some family members, but it is not yet clear if it represents a distinct pathway or if it can be integrated in the canonical pathway, as PKC seems to be required for Wnt-mediated inactivation of GSK-3 kinase. Both pathways seem to involve interactions with G-proteins. May be involved in transduction and intercellular transmission of polarity information during tissue morphogenesis and/or in differentiated tissues (Probable).[UniProtKB:Q8BKG4]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The lack of incorporating epitope information into the selection process makes the conventional antibody screening method less effective in identifying antibodies with desired functions. Here, we developed an epitope-directed antibody selection method by designing a directed library favoring the target epitope and a precise "counter" antigen for clearing irrelevant binders in the library. With this method, we successfully isolated an antibody, pF7_A5, that targets the less conserved region on the FZD2/7 CRD as designed. Guided by the structure of pF7_A5-FZD2(CRD), a further round of evolution was conducted together with the "counter" antigen selection strategy, and ultimately, an FZD2-specific antibody and an FZD7-preferred antibody were obtained. Because of targeting the predefined functional site, all these antibodies exhibited the expected modulatory activity on the Wnt pathway. Together, the method developed here will be useful in antibody drug discovery, and the identified FZD antibodies will have clinical potential in FZD-related cancer therapy.


Authors: Ge, Q.Q., Wang, Q.G.
An epitope-directed selection strategy facilitating the identification of Frizzled receptor selective antibodies.,Ge Q, Teng M, Li X, Guo Q, Tao Y Structure. 2023 Jan 5;31(1):33-43.e5. doi: 10.1016/j.str.2022.11.009. Epub 2022 , Dec 12. PMID:36513066<ref>PMID:36513066</ref>


Description: Frizzled10 CRD in complex with hB9L9.3 Fab
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Wang, Q.G]]
<div class="pdbe-citations 7x8t" style="background-color:#fffaf0;"></div>
[[Category: Ge, Q.Q]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ge Q]]
[[Category: Wang Q]]

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