8jfr
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==N-terminal domain of AcrIIA15 in complex with palindromic DNA substrate== | |
| + | <StructureSection load='8jfr' size='340' side='right'caption='[[8jfr]], [[Resolution|resolution]] 3.10Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[8jfr]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_delphini Staphylococcus delphini]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8JFR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8JFR 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]] 3.1Å</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=8jfr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8jfr OCA], [https://pdbe.org/8jfr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8jfr RCSB], [https://www.ebi.ac.uk/pdbsum/8jfr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8jfr ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | AcrIIA15 is an anti-CRISPR (Acr) protein that inhibits Staphylococcus aureus Cas9 (SaCas9). Although previous studies suggested it has dual functions, the structural and biochemical basis for its two activities remains unclear. Here, we determined the cryo-EM structure of AcrIIA15 in complex with SaCas9-sgRNA to reveal the inhibitory mechanism of the Acr's C-terminal domain (CTD) in mimicking dsDNA to block protospacer adjacent motif (PAM) recognition. For the N-terminal domain (NTD), our crystal structures of the AcrIIA15-promoter DNA show that AcrIIA15 dimerizes through its NTD to recognize double-stranded (ds) DNA. Further, AcrIIA15 can simultaneously bind to both SaCas9-sgRNA and promoter DNA, creating a supercomplex of two Cas9s bound to two CTDs converging on a dimer of the NTD bound to a dsDNA. These findings shed light on AcrIIA15's inhibitory mechanisms and its autoregulation of transcription, enhancing our understanding of phage-host interactions and CRISPR defense. | ||
| - | + | An anti-CRISPR that represses its own transcription while blocking Cas9-target DNA binding.,Deng X, Sun W, Li X, Wang J, Cheng Z, Sheng G, Wang Y Nat Commun. 2024 Feb 28;15(1):1806. doi: 10.1038/s41467-024-45987-5. PMID:38418450<ref>PMID:38418450</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| - | [[Category: Deng | + | <div class="pdbe-citations 8jfr" style="background-color:#fffaf0;"></div> |
| - | [[Category: Wang | + | == References == |
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Staphylococcus delphini]] | ||
| + | [[Category: Deng X]] | ||
| + | [[Category: Wang Y]] | ||
Current revision
N-terminal domain of AcrIIA15 in complex with palindromic DNA substrate
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