9k1t: Difference between revisions

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'''Unreleased structure'''


The entry 9k1t is ON HOLD  until Paper Publication
==Crystal structure of mouse granzyme A==
<StructureSection load='9k1t' size='340' side='right'caption='[[9k1t]], [[Resolution|resolution]] 2.18&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9k1t]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9K1T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9K1T 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]] 2.18&#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=9k1t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9k1t OCA], [https://pdbe.org/9k1t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9k1t RCSB], [https://www.ebi.ac.uk/pdbsum/9k1t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9k1t ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
In cellular immunity, cytotoxic lymphocytes employ granzyme A (GZMA) to cleave and activate the pore-forming protein gasdermin B (GSDMB) for the pyroptotic killing of target cells. How GZMA recognizes and cleaves GSDMB is unknown. Here, we show that human GZMA targets GSDMB via specific, high-affinity binding to its autoinhibitory GSDMB-C domain. This binding requires the dimerization of GZMA, a unique property among human granzymes. A crystal structure of the GZMA-GSDMB-C complex shows a 2:2 stoichiometry, featuring an exosite at each of the two symmetric dimer interfaces in GZMA. The exosite engages a two-loop-organized site in the GSDMB-C domain, rendering a functional cleavage at Lys244 in GSDMB. Mouse GZMA (mGZMA) adopts a similar dimer structure, but its exosite is less efficient in engaging GSDMB. Mutation of the exosite enabled mGZMA to efficiently cleave and activate GSDMB. Our study reveals a substrate-targeting mechanism used by lymphocyte-derived granzymes to kill target cells.


Authors:  
Exosite-mediated targeting of GSDMB by dimeric granzyme A in lymphocyte pyroptotic killing.,Zhong X, Su Y, Zhou Z, Sun Y, Hou Y, Shao F, Ding J Immunity. 2026 Feb 10;59(2):257-269.e6. doi: 10.1016/j.immuni.2025.12.009. Epub , 2026 Jan 26. PMID:41592574<ref>PMID:41592574</ref>


Description:  
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
<div class="pdbe-citations 9k1t" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Ding J]]
[[Category: Hou YJ]]
[[Category: Zhong X]]

Latest revision as of 07:07, 18 February 2026

Crystal structure of mouse granzyme A

9k1t, resolution 2.18Å

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