Modomics - A Database of RNA Modifications

ID Card:

Full name: Leucine carboxyl methyltransferase 2
Synonym: PPM2, LCMT2
GI: 1420038
Orf: YOL141W
UniProt: Q08282
Structures: | 2ZW9 | 2ZWA | 2ZZK |
Alpha Fold Predicted Structure: AF-Q08282-F1
Enzyme type: methyltransferase, carboxymethyltransferase
Position of modification - modification: t:37 - yW


PDB Structures:


2ZW9

Structure Description:

Title:
Classification:
Technique:

Abstract of the PDB Structure's related Publication:

Wybutosine (yW), one of the most complicated modified nucleosides, is found in the anticodon loop of eukaryotic phenylalanine tRNA. This hypermodified nucleoside ensures correct codon recognition by stabilizing codon-anticodon pairings during the decoding process in the ribosome. TYW4 is an S-adenosylmethionine (SAM)-dependent enzyme that catalyzes the final step of yW biosynthesis, methylation and methoxycarbonylation. However, the structural basis for the catalytic mechanism by TYW4, and especially that for the methoxycarbonylation, have remained elusive. Here we report the apo and cofactor-bound crystal structures of yeast TYW4. The structures revealed that the C-terminal domain folds into a beta-propeller structure, forming part of the binding pocket for the target nucleoside. A comparison of the apo, SAM-bound, and S-adenosylhomocysteine-bound structures of TYW4 revealed a drastic structural change upon cofactor binding, which may sequester solvent from the catalytic site during the reaction and facilitate product release after the reaction. In conjunction with the functional analysis, our results suggest that TYW4 catalyzes both methylation and methoxycarbonylation at a single catalytic site, and in the latter reaction, the methoxycarbonyl group is formed through the fixation of carbon dioxide.

Download RCSB-PDB Structures:

Pdb Files   2ZW9.pdb   2ZWA.pdb   2ZZK.pdb  
Pdbx/mmCIF Files   2ZW9.cif   2ZWA.cif   2ZZK.cif  


Protein sequence:

MKNLTTIKQTNKNVKQERRKKYADLAIQGTNNSSIASKRSVELLYLPKLSSANNFQMDKNNKLLEYFKFFVPKKIKRSPCINRGYWLRLFAIRSRLNSIIEQTPQDKKIVVVNLGCGYDPLPFQLLDTNNIQSQQYHDRVSFIDIDYSDLLKIKIELIKTIPELSKIIGLSEDKDYVDDSNVDFLTTPKYLARPCDLNDSKMFSTLLNECQLYDPNVVKVFVAEVSLAYMKPERSDSIIEATSKMENSHFIILEQLIPKGPFEPFSKQMLAHFKRNDSPLQSVLKYNTIESQVQRFNKLGFAYVNVGDMFQLWESADEATKKELLKVEPFDELEEFHLFCHHYVLCHATNYKEFAFTQGFLFDRSISEINLTVDEDYQLLECECPINRKFGDVDVAGNDVFYMGGSNPYRVNEILQMSIHYDKIDMKNIEVSSSEVPVARMCHTFTTISRNNQLLLIGGRKAPHQGLSDNWIFDMKTREWSMIKSLSHTRFRHSACSLPDGNVLILGGVTEGPAMLLYNVTEEIFKDVTPKDEFFQNSLVSAGLEFDPVSKQGIILGGGFMDQTTVSDKAIIFKYDAENATEPITVIKKLQHPLFQRYGSQIKYITPRKLLIVGGTSPSGLFDRTNSIISLDPLSETLTSIPISRRIWEDHSLMLAGFSLVSTSMGTIHIIGGGATCYGFGSVTNVGLKLIAIAK

Comments:

TYW4 is a Ado-Met-dependent carboxymethyltransferase. It catalyzes two reactions: methylation of the α-carboxy group of yW-72 to form yW-58 and methoxycarbonylation of α-amino group of yW-58 to complete yW. It is proposed that these two reactions are performed with a single catalytic site. The methoxycarbonylation reaction may proceed through carbamate formation with CO2 and methylation with SAM, which results in CO2 fixation




Reaction Substrate SubstrateType Position (Anti)Codon Modified (Anti)Codon Amino Acid Change Transcript Name Transcript Region Cellular Localization References
yW-58:yW RNA tRNA 37 #AA #AA tRNANone#AA anticodon-loop Mitochondrion 19287006   
yW-72:yW-58 RNA tRNA 37 #AA #AA tRNANone#AA anticodon-loop Mitochondrion 19287006   
yW-72:yW-58 RNA tRNA 37 #AA #AA tRNANone#AA anticodon-loop Mitochondrion 19287006   
yW-58:yW RNA tRNA 37 #AA #AA tRNANone#AA anticodon-loop Mitochondrion 19287006   

Alpha Fold Predicted Structure:






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Protein sequence:

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

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-Q08282-F1.pdb  
Alpha Fold Pdbx/mmCIF Files   AF-Q08282-F1.cif  
DSSP Secondary Structures   Q08282.dssp  





Publications:

Title Authors Journal Details PubMed Id DOI
Biosynthesis of wybutosine, a hyper-modified nucleoside in eukaryotic phenylalanine tRNA. Noma A, Kirino Y, Ikeuchi Y, Suzuki T EMBO J [details] 16642040 -
Structural basis of tRNA modification with CO2 fixation and methylation by wybutosine synthesizing enzyme TYW4. Suzuki Y, Noma A, Suzuki T, Ishitani R, Nureki O Nucleic Acids Res [details] 19287006 -

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