7dtr: Difference between revisions

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==Structure of an AcrIF protein==
==Structure of an AcrIF protein==
<StructureSection load='7dtr' size='340' side='right'caption='[[7dtr]]' scene=''>
<StructureSection load='7dtr' size='340' side='right'caption='[[7dtr]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7DTR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DTR FirstGlance]. <br>
<table><tr><td colspan='2'>[[7dtr]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7DTR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DTR FirstGlance]. <br>
</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=7dtr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dtr OCA], [https://pdbe.org/7dtr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dtr RCSB], [https://www.ebi.ac.uk/pdbsum/7dtr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dtr ProSAT]</span></td></tr>
</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=7dtr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dtr OCA], [https://pdbe.org/7dtr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dtr RCSB], [https://www.ebi.ac.uk/pdbsum/7dtr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dtr ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
CRISPR-Cas systems are prokaryotic adaptive immune systems and phages use anti-CRISPR proteins (Acrs) to counteract these systems. Here, we report the structures of AcrIF24 and its complex with the crRNA-guided surveillance (Csy) complex. The HTH motif of AcrIF24 can bind the Acr promoter region and repress its transcription, suggesting its role as an Aca gene in self-regulation. AcrIF24 forms a homodimer and further induces dimerization of the Csy complex. Apart from blocking the hybridization of target DNA to the crRNA, AcrIF24 also induces the binding of non-sequence-specific dsDNA to the Csy complex, similar to AcrIF9, although this binding seems to play a minor role in AcrIF24 inhibitory capacity. Further structural and biochemical studies of the Csy-AcrIF24-dsDNA complexes and of AcrIF24 mutants reveal that the HTH motif of AcrIF24 and the PAM recognition loop of the Csy complex are structural elements essential for this non-specific dsDNA binding. Moreover, AcrIF24 and AcrIF9 display distinct characteristics in inducing non-specific DNA binding. Together, our findings highlight a multifunctional Acr and suggest potential wide distribution of Acr-induced non-specific DNA binding.
Insights into the inhibition of type I-F CRISPR-Cas system by a multifunctional anti-CRISPR protein AcrIF24.,Yang L, Zhang L, Yin P, Ding H, Xiao Y, Zeng J, Wang W, Zhou H, Wang Q, Zhang Y, Chen Z, Yang M, Feng Y Nat Commun. 2022 Apr 11;13(1):1931. doi: 10.1038/s41467-022-29581-1. PMID:35411005<ref>PMID:35411005</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 7dtr" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Peipei Y]]
[[Category: Peipei, Y]]
[[Category: Yue F]]
[[Category: Yue, F]]
[[Category: Hth motif]]
[[Category: Protein interaction]]
[[Category: Viral protein]]