Summary information and primary citation
- PDB-id
-
8aw3;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- RNA binding protein
- Method
- cryo-EM (3.6 Å)
- Summary
- cryo-EM structure of the tb adat2-3 deaminase in
complex with trna
- Reference
-
Dolce LG, Zimmer AA, Tengo L, Weis F, Rubio MAT, Alfonzo
JD, Kowalinski E (2022): "Structural
basis for sequence-independent substrate selection by
eukaryotic wobble base tRNA deaminase ADAT2/3."
Nat Commun, 13, 6737. doi:
10.1038/s41467-022-34441-z.
- Abstract
- The essential deamination of adenosine
A<sub>34</sub> to inosine at the wobble base is
the individual tRNA modification with the greatest effects
on mRNA decoding, empowering a single tRNA to translate
three different codons. To date, many aspects of how
eukaryotic deaminases specifically select their multiple
substrates remain unclear. Here, using cryo-EM, we present
the structure of a eukaryotic ADAT2/3 deaminase bound to a
full-length tRNA, revealing that the enzyme distorts the
anticodon loop, but in contrast to the bacterial enzymes,
selects its substrate via sequence-independent contacts of
eukaryote-acquired flexible or intrinsically unfolded
motifs distal from the conserved catalytic core. A gating
mechanism for substrate entry to the active site is
identified. Our multi-step tRNA recognition model yields
insights into how RNA editing by A<sub>34</sub>
deamination evolved, shaped the genetic code, and directly
impacts the eukaryotic proteome.