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1 58-nt fragment that is the binding domain of ribosomal protein L11.
2  the human homologue of MDM2, HDM2, binds to ribosomal protein L11.
3 n has been purified and characterized as the ribosomal protein L11.
4 otide fragment of 23S ribosomal RNA bound to ribosomal protein L11.
5 ructure is a prerequisite for recognition by ribosomal protein L11.
6 part of a domain targeted by antibiotics and ribosomal protein L11.
7                           Here, we show that ribosomal protein L11, a component of the large subunit
8 sing ribosomes containing either Cy3-labeled ribosomal protein L11 and A- or P-site Cy5-labeled tRNA
9                                              Ribosomal protein L11 and its associated binding site on
10 High-resolution structures reveal that yeast ribosomal protein L11 and its bacterial/archael homologs
11                                              Ribosomal protein L11 and the L11 binding region of ribo
12 RNA variants using UV melting and binding of ribosomal protein L11 and thiostrepton to assay for tert
13 e found hBH bound to human homologues of rat ribosomal proteins L11 and L29.
14 n in bacterial 23S rRNA is directly bound by ribosomal protein L11, and this complex is essential to
15                                          The ribosomal protein L11 binds to and suppresses the E3 lig
16                                              Ribosomal protein L11 consists of a C-terminal and an N-
17 , as with the E. coli methyltransferase, the ribosomal protein L11 dissociated from ribosomes is a mo
18  ribosomal RNA and the RNA-binding domain of ribosomal protein L11 has been solved at 2.8 angstrom re
19                                              Ribosomal protein L11 has two domains: the C-terminal do
20 istone-like DNA-binding protein HU (HP0835); ribosomal protein L11 (HP1202); a putative outer membran
21                                          The ribosomal protein L11 in bacteria is posttranslationally
22 p53 in response to oncogenic stress, whereas ribosomal protein L11 induces p53 following ribosomal st
23                     We previously found that ribosomal protein L11 inhibits c-Myc activity by blockin
24                                              Ribosomal protein L11 interacts with a 58-nucleotide dom
25                                              Ribosomal protein L11 is a highly conserved protein that
26                                    Bacterial ribosomal protein L11 is post-translationally trimethyla
27 aracterized C-terminal RNA binding domain of ribosomal protein L11 (L11-C76) and its 58 nucleotide bi
28 scopy of the 75 residue C-terminal domain of ribosomal protein L11 (L11-C76) in its RNA-bound state.
29                     The C-terminal domain of ribosomal protein L11, L11-C76, binds in the distorted m
30  domain of EF-G and the N-terminal domain of ribosomal protein L11 occurs within two rapidly intercon
31                           Here, we show that ribosomal protein L11 regulates c-myc mRNA turnover.
32                                              Ribosomal protein L11 (RPL11) has been shown to activate
33  nuclear-specific association of PRAS40 with ribosomal protein L11 (RPL11).
34  antibiotic thiostrepton, due to the loss of ribosomal protein L11 (RplK), were found to be blocked i
35 of these effects appeared to be titration of ribosomal protein L11, since normal phenotypes could be
36  that it is precisely the N-terminal part of ribosomal protein L11 that is required for the functiona
37 uctural components, the N-terminal domain of ribosomal protein L11, the C-terminal domain of ribosoma
38 0 S ribosome, isolated from a mutant lacking ribosomal protein L11, with the three-dimensional map of
39  regulates tumor suppressor p53 by tethering ribosomal protein L11 within the nucleolus to repress th