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Crystal Structure of an RluF-RNA Complex: A Base-Pair Rearrangement Is the Key to Selectivity of RluF for U2604 of the Ribosome
Authors:Akram Alian
Institution:Department of Biochemistry and Biophysics, University of California, San Francisco, 600 16th Street, Room S412C, MC2240, San Francisco, CA 94158-2517, USA
Abstract:Escherichia coli pseudouridine synthase RluF is dedicated to modifying U2604 in a stem-loop of 23S RNA, while a homologue, RluB, modifies the adjacent base, U2605. Both uridines are in the same RNA stem, separated by ∼ 4 Å. The 3.0 Å X-ray crystal structure of RluF bound to the isolated stem-loop, in which U2604 is substituted by 5-fluorouridine to prevent catalytic turnover, shows RluF distinguishes closely spaced bases in similar environments by a selectivity mechanism based on a frameshift in base pairing. The RNA stem-loop is bound to a conserved binding groove in the catalytic domain. A base from a bulge in the stem, A2602, has folded into the stem, forcing one strand of the RNA stem to translate by one position and thus positioning U2604 to flip into the active site. RluF does not modify U2604 in mutant stem-loops that lack the A2602 bulge and shows dramatically higher activity for a stem-loop with a mutation designed to facilitate A2602 refolding into the stem with concomitant RNA strand translation. Residues whose side chains contact rearranged bases in the bound stem-loop, while conserved among RluFs, are not conserved between RluFs and RluBs, suggesting that RluB does not bind to the rearranged stem loop.
Keywords:Ψ  pseudouridine  S4-like domain  domain with the same fold as the RNA-binding domain of ribosomal protein S4  ΔRluF  N-terminal truncation of RluF  C05  stem-loop mutant U2605C  C04  stem-loop mutant U2604C  C05G89  stem-loop mutant (U2605C  A2589G)  C04G90  stem-loop mutant (U2604C  A2590G)  Δ02  A2602 deletion  rRNA  ribosomal RNA  NCS  noncrystallographic symmetry
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