4GKJ
Structure of the Thermus thermophilus 30S ribosomal subunit complexed with a human mitochondrial anticodon stem loop (ASL) of transfer RNA Methionine (TRNAMET) bound to an mRNA with an AUG-codon in the A-site and paromomycin.
Summary for 4GKJ
Entry DOI | 10.2210/pdb4gkj/pdb |
Related | 2KRY 2UUC 3T1Y |
Descriptor | 16S rRNA, 30S ribosomal protein S10, 30S ribosomal protein S11, ... (26 entities in total) |
Functional Keywords | translation initiation, 5-formylcytidine, ribosome-antibiotic complex, ribosome/antibiotic |
Biological source | Thermus thermophilus More |
Total number of polymer chains | 23 |
Total formula weight | 777325.73 |
Authors | Cantara, W.A.,Murphy IV, F.V.,Spears, J.L.,Demirci, H.,Agris, P.F. (deposition date: 2012-08-11, release date: 2013-06-05, Last modification date: 2024-02-28) |
Primary citation | Cantara, W.A.,Murphy, F.V.,Demirci, H.,Agris, P.F. Expanded use of sense codons is regulated by modified cytidines in tRNA. Proc.Natl.Acad.Sci.USA, 110:10964-10969, 2013 Cited by PubMed Abstract: Codon use among the three domains of life is not confined to the universal genetic code. With only 22 tRNA genes in mammalian mitochondria, exceptions from the universal code are necessary for proper translation. A particularly interesting deviation is the decoding of the isoleucine AUA codon as methionine by the one mitochondrial-encoded tRNA(Met). This tRNA decodes AUA and AUG in both the A- and P-sites of the metazoan mitochondrial ribosome. Enrichment of posttranscriptional modifications is a commonly appropriated mechanism for modulating decoding rules, enabling some tRNA functions while restraining others. In this case, a modification of cytidine, 5-formylcytidine (f(5)C), at the wobble position-34 of human mitochondrial tRNA(f5CAU)(Met) (hmtRNA(f5CAU)(Met)) enables expanded decoding of AUA, resulting in a deviation in the genetic code. Visualization of the codon•anticodon interaction by X-ray crystallography revealed that recognition of both A and G at the third position of the codon occurs in the canonical Watson-Crick geometry. A modification-dependent shift in the tautomeric equilibrium toward the rare imino-oxo tautomer of cytidine stabilizes the f(5)C34•A base pair geometry with two hydrogen bonds. PubMed: 23781103DOI: 10.1073/pnas.1222641110 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.298 Å) |
Structure validation
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