6ZMB
Structure of the native tRNA-Monooxygenase enzyme MiaE
Summary for 6ZMB
Entry DOI | 10.2210/pdb6zmb/pdb |
Descriptor | tRNA hydroxylase, FE (III) ION, CHLORIDE ION, ... (10 entities in total) |
Functional Keywords | trna-monooxygenase metallo-enzyme trna-modifying enzyme hydroxylase, oxidoreductase |
Biological source | Pseudomonas putida KT2440 |
Total number of polymer chains | 2 |
Total formula weight | 46873.95 |
Authors | Carpentier, P.,Atta, M. (deposition date: 2020-07-02, release date: 2020-09-02, Last modification date: 2024-01-31) |
Primary citation | Carpentier, P.,Lepretre, C.,Basset, C.,Douki, T.,Torelli, S.,Duarte, V.,Hamdane, D.,Fontecave, M.,Atta, M. Structural, biochemical and functional analyses of tRNA-monooxygenase enzyme MiaE from Pseudomonas putida provide insights into tRNA/MiaE interaction. Nucleic Acids Res., 48:9918-9930, 2020 Cited by PubMed Abstract: MiaE (2-methylthio-N6-isopentenyl-adenosine37-tRNA monooxygenase) is a unique non-heme diiron enzyme that catalyzes the O2-dependent post-transcriptional allylic hydroxylation of a hypermodified nucleotide 2-methylthio-N6-isopentenyl-adenosine (ms2i6A37) at position 37 of selected tRNA molecules to produce 2-methylthio-N6-4-hydroxyisopentenyl-adenosine (ms2io6A37). Here, we report the in vivo activity, biochemical, spectroscopic characterization and X-ray crystal structure of MiaE from Pseudomonas putida. The investigation demonstrates that the putative pp-2188 gene encodes a MiaE enzyme. The structure shows that Pp-MiaE consists of a catalytic diiron(III) domain with a four alpha-helix bundle fold. A docking model of Pp-MiaE in complex with tRNA, combined with site directed mutagenesis and in vivo activity shed light on the importance of an additional linker region for substrate tRNA recognition. Finally, krypton-pressurized Pp-MiaE experiments, revealed the presence of defined O2 site along a conserved hydrophobic tunnel leading to the diiron active center. PubMed: 32785618DOI: 10.1093/nar/gkaa667 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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