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8d9i

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(New page: '''Unreleased structure''' The entry 8d9i is ON HOLD Authors: Description: Category: Unreleased Structures)
Current revision (08:17, 14 June 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8d9i is ON HOLD
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==gRAMP non-matching PFS-with Mg==
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<StructureSection load='8d9i' size='340' side='right'caption='[[8d9i]], [[Resolution|resolution]] 3.62&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8d9i]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Candidatus_Scalindua_brodae Candidatus Scalindua brodae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8D9I OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8D9I FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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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=8d9i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8d9i OCA], [https://pdbe.org/8d9i PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8d9i RCSB], [https://www.ebi.ac.uk/pdbsum/8d9i PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8d9i ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/A0A0B0EGF3_9BACT A0A0B0EGF3_9BACT]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The Type III-E RNA-targeting effector complex (gRAMP/Cas7-11) is associated with a caspase-like protein (TPR-CHAT/Csx29) to form Craspase (CRISPR-guided caspase). Here we use cryo-electron microscopy snapshots of Craspase to explain its target RNA cleavage and protease activation mechanisms. Target-guide pairing extending into the 5' region of the guide RNA displaces a gating loop in gRAMP, which triggers an extensive conformational relay that allosterically aligns the protease catalytic dyad and opens an amino acid sidechain-binding pocket. We further define Csx30 as the endogenous protein substrate that is site-specifically proteolyzed by RNA-activated Craspase. This protease activity is switched off by target RNA cleavage by gRAMP, and is not activated by RNA targets containing a matching protospacer flanking sequence. We thus conclude that Craspase is a target RNA-activated protease with self-regulatory capacity.
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Authors:
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Craspase is a CRISPR RNA-guided, RNA-activated protease.,Hu C, van Beljouw SPB, Nam KH, Schuler G, Ding F, Cui Y, Rodriguez-Molina A, Haagsma AC, Valk M, Pabst M, Brouns SJJ, Ke A Science. 2022 Aug 25:eadd5064. doi: 10.1126/science.add5064. PMID:36007061<ref>PMID:36007061</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 8d9i" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Candidatus Scalindua brodae]]
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[[Category: Large Structures]]
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[[Category: Hu C]]
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[[Category: Ke A]]
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[[Category: Nam KH]]
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[[Category: Schuler G]]

Current revision

gRAMP non-matching PFS-with Mg

PDB ID 8d9i

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