Modomics - A Database of RNA Modifications

ID Card:

Full name: tRNA(Ile)2-lysidine synthase
Synonym: GK0060
GI: 56418595
COG: COG0037
UniProt: Q5L3T3
Structures: | 3A2K | 3HJ7 |
Alpha Fold Predicted Structure: AF-Q5L3T3-F1
Enzyme type: lysidine synthase
Position of modification - modification: t:34 - k2C


PDB Structures:


3A2K

Structure Description:

Title:
Classification:
Technique:

Abstract of the PDB Structure's related Publication:

Maturation of precursor transfer RNA (pre-tRNA) includes excision of the 5' leader and 3' trailer sequences, removal of introns and addition of the CCA terminus. Nucleotide modifications are incorporated at different stages of tRNA processing, after the RNA molecule adopts the proper conformation. In bacteria, tRNA(Ile2) lysidine synthetase (TilS) modifies cytidine into lysidine (L; 2-lysyl-cytidine) at the first anticodon of tRNA(Ile2) (refs 4-9). This modification switches tRNA(Ile2) from a methionine-specific to an isoleucine-specific tRNA. However, the aminoacylation of tRNA(Ile2) by methionyl-tRNA synthetase (MetRS), before the modification by TilS, might lead to the misincorporation of methionine in response to isoleucine codons. The mechanism used by bacteria to avoid this pitfall is unknown. Here we show that the TilS enzyme specifically recognizes and modifies tRNA(Ile2) in its precursor form, thereby avoiding translation errors. We identified the lysidine modification in pre-tRNA(Ile2) isolated from RNase-E-deficient Escherichia coli and did not detect mature tRNA(Ile2) lacking this modification. Our kinetic analyses revealed that TilS can modify both types of RNA molecule with comparable efficiencies. X-ray crystallography and mutational analyses revealed that TilS specifically recognizes the entire L-shape structure in pre-tRNA(Ile2) through extensive interactions coupled with sequential domain movements. Our results demonstrate how TilS prevents the recognition of tRNA(Ile2) by MetRS and achieves high specificity for its substrate. These two key points form the basis for maintaining the fidelity of isoleucine codon translation in bacteria. Our findings also provide a rationale for the necessity of incorporating specific modifications at the precursor level during tRNA biogenesis.

Download RCSB-PDB Structures:

Pdb Files   3A2K.pdb   3HJ7.pdb  
Pdbx/mmCIF Files   3A2K.cif   3HJ7.cif  


Protein sequence:

MIDKVRAFIHRHQLLSEGAAVIVGVSGGPDSLALLHVFLSLRDEWKLQVIAAHVDHMFRGRESEEEMEFVKRFCVERRILCETAQIDVPAFQRSAGLGAQEAARICRYRFFAELMEKHQAGYVAVGHHGDDQVETILMRLVRGSTSKGYAGIPVKRPFHGGYLIRPFLAVSRAEIEAYCRQMGLSPRCDPSNEKDDYTRNRFRHHIVPLLRQENPRLHERFQQYSEMMAEDEQFLEELAADALNKVMEKQHRDAALSIGPFLELPRPLQRRVLQLLLLRLYGGVPPTLTSVHIGHILMLCERGRPSGMIDLPKGLKVIRSYDRCLFTFDAESGEKGYWFELPVPALLPLPNGYAIISEFGEHYPRKQAGNDWFVVDPASVSLPLRVRTRRRGDRMVLKGTGGTKKLKEIFIEAKIPRMERDRWPIVEDADGRILWVPGLKKSAFEAQNRGQARYILLQYQAMNS

Comments:

The activity was tested only in vitro




Reaction Substrate SubstrateType Position (Anti)Codon Modified (Anti)Codon Amino Acid Change Transcript Name Transcript Region Cellular Localization References
C:k2C RNA tRNA 34 CAU }AU tRNAIleCAU wobble - position Prokaryotic Cytosol 19847269   

Alpha Fold Predicted Structure:






Clear Selection and Reset Camera

Protein sequence:

M I D K V R A F I H R H Q L L S E G A A V I V G V S G G P D S L A L L H V F L S L R D E W K L Q V I A A H V D H M F R G R E S E E E M E F V K R F C V E R R I L C E T A Q I D V P A F Q R S A G L G A Q E A A R I C R Y R F F A E L M E K H Q A G Y V A V G H H G D D Q V E T I L M R L V R G S T S K G Y A G I P V K R P F H G G Y L I R P F L A V S R A E I E A Y C R Q M G L S P R C D P S N E K D D Y T R N R F R H H I V P L L R Q E N P R L H E R F Q Q Y S E M M A E D E Q F L E E L A A D A L N K V M E K Q H R D A A L S I G P F L E L P R P L Q R R V L Q L L L L R L Y G G V P P T L T S V H I G H I L M L C E R G R P S G M I D L P K G L K V I R S Y D R C L F T F D A E S G E K G Y W F E L P V P A L L P L P N G Y A I I S E F G E H Y P R K Q A G N D W F V V D P A S V S L P L R V R T R R R G D R M V L K G T G G T K K L K E I F I E A K I P R M E R D R W P I V E D A D G R I L W V P G L K K S A F E A Q N R G Q A R Y I L L Q Y Q A M N S

Secondary Structure Alphabet

  • G: 3-turn helix (310helix)
  • H: α-helix
  • I: 𝝅-helix (5 - turn helix)
  • T: Hydrogen Bonded Turn
  • B: β-sheet
  • S: Bend
  • C: Coil (residues not present in any of the above conformations)
  • N: Not assigned

Download PDB Structures & DSSP Secondary Structures:

Alpha Fold Pdb Files   AF-Q5L3T3-F1.pdb  
Alpha Fold Pdbx/mmCIF Files   AF-Q5L3T3-F1.cif  
DSSP Secondary Structures   Q5L3T3.dssp  





Publications:

Title Authors Journal Details PubMed Id DOI
Structural basis for translational fidelity ensured by transfer RNA lysidine synthetase. Nakanishi K, Bonnefond L, Kimura S, Suzuki T, Ishitani R, Nureki O Nature [details] 19847269 -