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4N41

Structure of Thermus thermophilus Argonaute bound to guide DNA and 15-mer target DNA

Summary for 4N41
Entry DOI10.2210/pdb4n41/pdb
Related3DLH 3HM9 3HVR 4N47 4N76 4NCA 4NCB
DescriptorArgonaute, 5'-D(P*TP*GP*AP*GP*GP*TP*AP*GP*TP*AP*GP*GP*TP*T*GP*TP*AP*TP*AP*GP*T)-3', 5'-D(P*AP*CP*CP*TP*AP*CP*TP*AP*CP*CP*TP*CP*G)-3', ... (6 entities in total)
Functional Keywordsargonaute, rna interference, dna interference, nuclear protein-dna complex, nuclear protein/dna
Biological sourceThermus thermophilus
Total number of polymer chains6
Total formula weight174763.20
Authors
Sheng, G.,Zhao, H.,Wang, J.,Rao, Y.,Wang, Y. (deposition date: 2013-10-08, release date: 2014-01-15, Last modification date: 2023-09-20)
Primary citationSheng, G.,Zhao, H.,Wang, J.,Rao, Y.,Tian, W.,Swarts, D.C.,van der Oost, J.,Patel, D.J.,Wang, Y.
Structure-based cleavage mechanism of Thermus thermophilus Argonaute DNA guide strand-mediated DNA target cleavage.
Proc.Natl.Acad.Sci.USA, 111:652-657, 2014
Cited by
PubMed Abstract: We report on crystal structures of ternary Thermus thermophilus Argonaute (TtAgo) complexes with 5'-phosphorylated guide DNA and a series of DNA targets. These ternary complex structures of cleavage-incompatible, cleavage-compatible, and postcleavage states solved at improved resolution up to 2.2 Å have provided molecular insights into the orchestrated positioning of catalytic residues, a pair of Mg(2+) cations, and the putative water nucleophile positioned for in-line attack on the cleavable phosphate for TtAgo-mediated target cleavage by a RNase H-type mechanism. In addition, these ternary complex structures have provided insights into protein and DNA conformational changes that facilitate transition between cleavage-incompatible and cleavage-compatible states, including the role of a Glu finger in generating a cleavage-competent catalytic Asp-Glu-Asp-Asp tetrad. Following cleavage, the seed segment forms a stable duplex with the complementary segment of the target strand.
PubMed: 24374628
DOI: 10.1073/pnas.1321032111
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.248 Å)
Structure validation

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