6sce

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
m (Protected "6sce" [edit=sysop:move=sysop])
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 6sce is ON HOLD
+
==Structure of a Type III CRISPR defence DNA nuclease activated by cyclic oligoadenylate==
 +
<StructureSection load='6sce' size='340' side='right'caption='[[6sce]], [[Resolution|resolution]] 1.83&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[6sce]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6SCE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6SCE FirstGlance]. <br>
 +
</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
 +
<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=6sce FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6sce OCA], [http://pdbe.org/6sce PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6sce RCSB], [http://www.ebi.ac.uk/pdbsum/6sce PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6sce ProSAT]</span></td></tr>
 +
</table>
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
The CRISPR system provides adaptive immunity against mobile genetic elements in prokaryotes. On binding invading RNA species, Type III CRISPR systems generate cyclic oligoadenylate (cOA) signalling molecules, potentiating a powerful immune response by activating downstream effector proteins, leading to viral clearance, cell dormancy or death. Here we describe the structure and mechanism of a cOA-activated CRISPR defence DNA endonuclease, CRISPR ancillary nuclease 1 (Can1). Can1 has a unique monomeric structure with two CRISPR associated Rossman fold (CARF) domains and two DNA nuclease-like domains. The crystal structure of the enzyme has been captured in the activated state, with a cyclic tetra-adenylate (cA4) molecule bound at the core of the protein. cA4 binding reorganises the structure to license a metal-dependent DNA nuclease activity specific for nicking of supercoiled DNA. DNA nicking by Can1 is predicted to slow down viral replication kinetics by leading to the collapse of DNA replication forks.
-
Authors:
+
Structure and mechanism of a Type III CRISPR defence DNA nuclease activated by cyclic oligoadenylate.,McMahon SA, Zhu W, Graham S, Rambo R, White MF, Gloster TM Nat Commun. 2020 Jan 24;11(1):500. doi: 10.1038/s41467-019-14222-x. PMID:31980625<ref>PMID:31980625</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 6sce" style="background-color:#fffaf0;"></div>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Large Structures]]
 +
[[Category: Gloster, T M]]
 +
[[Category: Graham, S]]
 +
[[Category: McMahon, S A]]
 +
[[Category: White, M F]]
 +
[[Category: Zhu, W]]
 +
[[Category: Crispr carf dna nuclease cyclic oligoadenylate thermus thermophilus]]
 +
[[Category: Dna]]

Revision as of 06:34, 19 February 2020

Structure of a Type III CRISPR defence DNA nuclease activated by cyclic oligoadenylate

PDB ID 6sce

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools