6je4

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'''Unreleased structure'''
 
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The entry 6je4 is ON HOLD until Paper Publication
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==Crystal structure of Nme1Cas9-sgRNA-dsDNA dimer mediated by double protein inhibitor AcrIIC3 monomers==
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<StructureSection load='6je4' size='340' side='right'caption='[[6je4]], [[Resolution|resolution]] 3.07&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6je4]] is a 20 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6JE4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6JE4 FirstGlance]. <br>
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Description:
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6je4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6je4 OCA], [http://pdbe.org/6je4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6je4 RCSB], [http://www.ebi.ac.uk/pdbsum/6je4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6je4 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/CAS9_NEIM8 CAS9_NEIM8]] CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein, although RNase 3 is not required for 5'-processing of crRNA in this strain. Cas9/crRNA/tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer; Cas9 is inactive in the absence of the 2 guide RNAs (gRNA, PubMed:23940360). Cas9 recognizes the protospacer adjacent motif (PAM) in the CRISPR repeat sequences to help distinguish self versus nonself, as targets within the bacterial CRISPR locus do not have PAMs. PAM recognition is also required for catalytic activity. Plasmids containing sequences homologous to endogenous spacer elements and that have flanking PAM consensus sequences cannot transform this strain unless the cas9 gene is disrupted or critical residues of Cas9 are mutated.<ref>PMID:23706818</ref> <ref>PMID:23940360</ref>
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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: Large Structures]]
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[[Category: Cheng, Z]]
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[[Category: Huang, X]]
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[[Category: Liu, C]]
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[[Category: Sun, W]]
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[[Category: Wang, K]]
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[[Category: Wang, Y]]
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[[Category: Yang, J]]
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[[Category: Acriic3]]
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[[Category: Anti-crispr]]
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[[Category: Crispr-cas9]]
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[[Category: Hydrolase]]
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[[Category: Hydrolase-hydrolase inhibitor-dna-rna complex]]
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[[Category: Nme1cas9]]
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[[Category: Nmecas9]]

Revision as of 06:39, 6 November 2019

Crystal structure of Nme1Cas9-sgRNA-dsDNA dimer mediated by double protein inhibitor AcrIIC3 monomers

PDB ID 6je4

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