4F1N
Crystal structure of Kluyveromyces polysporus Argonaute with a guide RNA
Summary for 4F1N
| Entry DOI | 10.2210/pdb4f1n/pdb |
| Descriptor | KpAGO, RNA 5'-R(P*UP*AP*AP*AP*AP*AP*AP*AP*A)-3' (3 entities in total) |
| Functional Keywords | argonaute, rnai, rnase h, rna binding protein-rna complex, rna binding protein/rna |
| Biological source | Vanderwaltozyma polyspora More |
| Total number of polymer chains | 4 |
| Total formula weight | 241390.63 |
| Authors | Nakanishi, K.,Weinberg, D.E.,Bartel, D.P.,Patel, D.J. (deposition date: 2012-05-07, release date: 2012-06-13, Last modification date: 2024-02-28) |
| Primary citation | Nakanishi, K.,Weinberg, D.E.,Bartel, D.P.,Patel, D.J. Structure of yeast Argonaute with guide RNA. Nature, 486:368-374, 2012 Cited by PubMed Abstract: The RNA-induced silencing complex, comprising Argonaute and guide RNA, mediates RNA interference. Here we report the 3.2 Å crystal structure of Kluyveromyces polysporus Argonaute (KpAGO) fortuitously complexed with guide RNA originating from small-RNA duplexes autonomously loaded by recombinant KpAGO. Despite their diverse sequences, guide-RNA nucleotides 1-8 are positioned similarly, with sequence-independent contacts to bases, phosphates and 2'-hydroxyl groups pre-organizing the backbone of nucleotides 2-8 in a near-A-form conformation. Compared with prokaryotic Argonautes, KpAGO has numerous surface-exposed insertion segments, with a cluster of conserved insertions repositioning the N domain to enable full propagation of guide-target pairing. Compared with Argonautes in inactive conformations, KpAGO has a hydrogen-bond network that stabilizes an expanded and repositioned loop, which inserts an invariant glutamate into the catalytic pocket. Mutation analyses and analogies to ribonuclease H indicate that insertion of this glutamate finger completes a universally conserved catalytic tetrad, thereby activating Argonaute for RNA cleavage. PubMed: 22722195DOI: 10.1038/nature11211 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.187 Å) |
Structure validation
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