4KRE
Structure of Human Argonaute-1 bound to endogenous Sf9 RNA
Summary for 4KRE
Entry DOI | 10.2210/pdb4kre/pdb |
Related | 4KRF |
Descriptor | Protein argonaute-1, RNA (5'-R(P*AP*AP*UP*AP*UP*UP*AP*AP*A*AP*AP*AP*AP*AP*AP*AP*AP*AP*AP*A)-3') (3 entities in total) |
Functional Keywords | eukaryotic argonaute, gene regulation, rnai, slicer, transcription-rna complex, transcription/rna |
Biological source | Homo sapiens (human) More |
Cellular location | Cytoplasm, P-body: Q9UL18 |
Total number of polymer chains | 2 |
Total formula weight | 103890.41 |
Authors | Faehnle, C.R.,Elkayam, E.,Joshua-Tor, L. (deposition date: 2013-05-16, release date: 2013-06-19, Last modification date: 2024-02-28) |
Primary citation | Faehnle, C.R.,Elkayam, E.,Haase, A.D.,Hannon, G.J.,Joshua-Tor, L. The making of a slicer: activation of human argonaute-1. Cell Rep, 3:1901-1909, 2013 Cited by PubMed Abstract: Argonautes are the central protein component in small RNA silencing pathways. Of the four human Argonautes (hAgo1-hAgo4) only hAgo2 is an active slicer. We determined the structure of hAgo1 bound to endogenous copurified RNAs to 1.75 Å resolution and hAgo1 loaded with let-7 microRNA to 2.1 Å. Both structures are strikingly similar to the structures of hAgo2. A conserved catalytic tetrad within the PIWI domain of hAgo2 is required for its slicing activity. Completion of the tetrad, combined with a mutation on a loop adjacent to the active site of hAgo1, results in slicer activity that is substantially enhanced by swapping in the N domain of hAgo2. hAgo3, with an intact tetrad, becomes an active slicer by swapping the N domain of hAgo2 without additional mutations. Intriguingly, the elements that make Argonaute an active slicer involve a sophisticated interplay between the active site and more distant regions of the enzyme. PubMed: 23746446DOI: 10.1016/j.celrep.2013.05.033 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.754 Å) |
Structure validation
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