6c66: Difference between revisions
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==CRISPR RNA-guided surveillance complex, pre-nicking== | ==CRISPR RNA-guided surveillance complex, pre-nicking== | ||
<StructureSection load='6c66' size='340' side='right' caption='[[6c66]], [[Resolution|resolution]] 3.66Å' scene=''> | <StructureSection load='6c66' size='340' side='right'caption='[[6c66]], [[Resolution|resolution]] 3.66Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6c66]] is a 15 chain structure with sequence from [http://en.wikipedia.org/wiki/ ] and [http://en.wikipedia.org/wiki/Thefy Thefy]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6C66 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6C66 FirstGlance]. <br> | <table><tr><td colspan='2'>[[6c66]] is a 15 chain structure with sequence from [http://en.wikipedia.org/wiki/ ] and [http://en.wikipedia.org/wiki/Thefy Thefy]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6C66 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6C66 FirstGlance]. <br> | ||
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==See Also== | ==See Also== | ||
*[[CRISPR type I-E (Cascade)|CRISPR type I-E (Cascade)]] | *[[CRISPR type I-E (Cascade)|CRISPR type I-E (Cascade)]] | ||
*[[Helicase 3D structures|Helicase 3D structures]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | |||
[[Category: Thefy]] | [[Category: Thefy]] | ||
[[Category: Ke, A]] | [[Category: Ke, A]] |
Revision as of 12:31, 18 December 2019
CRISPR RNA-guided surveillance complex, pre-nickingCRISPR RNA-guided surveillance complex, pre-nicking
Structural highlights
Publication Abstract from PubMedType I CRISPR-Cas system features a sequential target-searching and degradation process on double-stranded DNA, by the RNA-guided Cascade complex and the nuclease-helicase fusion enzyme Cas3, respectively. Here we present a 3.7 A resolution cryo-EM structure of the Type I-E Cascade/R-loop/Cas3 complex, poised to initiate DNA degradation. Cas3 distinguishes Cascade conformations and only captures the R-loop forming Cascade, to avoid cleaving partially complementary targets. Its nuclease domain recruits the non-target strand (NTS) DNA at a bulged region for the nicking of single-stranded DNA. An additional 4.7 A resolution cryo-EM structure captures the post-nicking state, in which the severed NTS retracts to the helicase entrance, to be threaded for ATP-dependent processive degradation. These snapshots form the basis for understanding RNA-guided DNA degradation in Type I-E CRISPR-Cas systems. Structure basis for RNA-guided DNA degradation by Cascade and Cas3.,Xiao Y, Luo M, Dolan AE, Liao M, Ke A Science. 2018 Jun 7. pii: science.aat0839. doi: 10.1126/science.aat0839. PMID:29880725[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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