9GMX
SLFN11 WT dimer bound to tRNA-Leu-TAA (post-cleavage state)
Summary for 9GMX
Entry DOI | 10.2210/pdb9gmx/pdb |
Related | 9ERD 9ERE 9ERF |
EMDB information | 51457 |
Descriptor | RNA (5'-R(P*CP*CP*UP*GP*GP*UP*AP*CP*CP*A)-3'), Schlafen family member 11, RNA (76-MER), ... (6 entities in total) |
Functional Keywords | trna, endoribonuclease activity, dimeric, hydrolase |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 4 |
Total formula weight | 240409.24 |
Authors | Kugler, M.,Metzner, F.J.,Lammens, K. (deposition date: 2024-08-29, release date: 2024-12-11, Last modification date: 2024-12-18) |
Primary citation | Kugler, M.,Metzner, F.J.,Witte, G.,Hopfner, K.P.,Lammens, K. Phosphorylation-mediated conformational change regulates human SLFN11. Nat Commun, 15:10500-10500, 2024 Cited by PubMed Abstract: Human Schlafen 11 (SLFN11) is sensitizing cells to DNA damaging agents by irreversibly blocking stalled replication forks, making it a potential predictive biomarker in chemotherapy. Furthermore, SLFN11 acts as a pattern recognition receptor for single-stranded DNA (ssDNA) and functions as an antiviral restriction factor, targeting translation in a codon-usage-dependent manner through its endoribonuclease activity. However, the regulation of the various SLFN11 functions and enzymatic activities remains enigmatic. Here, we present cryo-electron microscopy (cryo-EM) structures of SLFN11 bound to tRNA-Leu and tRNA-Met that give insights into tRNA binding and cleavage, as well as its regulation by phosphorylation at S219 and T230. SLFN11 phosphomimetic mutant S753D adopts a monomeric conformation, shows ATP binding, but loses its ability to bind ssDNA and shows reduced ribonuclease activity. Thus, the phosphorylation site S753 serves as a conformational switch, regulating SLFN11 dimerization, as well as ATP and ssDNA binding, while S219 and T230 regulate tRNA recognition and nuclease activity. PubMed: 39627193DOI: 10.1038/s41467-024-54833-7 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.82 Å) |
Structure validation
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