3GVN
The 1.2 Angstroem crystal structure of an E.coli tRNASer acceptor stem microhelix reveals two magnesium binding sites
Summary for 3GVN
| Entry DOI | 10.2210/pdb3gvn/pdb |
| Related | 1SER 2V6W |
| Descriptor | 5'-R(*GP*GP*UP*GP*AP*GP*G)-3', 5'-R(*CP*CP*UP*CP*AP*CP*C)-3', MAGNESIUM ION, ... (4 entities in total) |
| Functional Keywords | trnaser/seryl-trna-synthetase, trna acceptor stem microhelix, identity elements, rna hydration, magnesium binding sites, rna |
| Total number of polymer chains | 2 |
| Total formula weight | 4481.38 |
| Authors | Eichert, A.,Furste, J.P.,Schreiber, A.,Perbandt, M.,Betzel, C.,Erdmann, V.A.,Forster, C. (deposition date: 2009-03-31, release date: 2009-07-28, Last modification date: 2023-11-01) |
| Primary citation | Eichert, A.,Furste, J.P.,Schreiber, A.,Perbandt, M.,Betzel, C.,Erdmann, V.A.,Forster, C. The 1.2A crystal structure of an E. coli tRNASer)acceptor stem microhelix reveals two magnesium binding sites. Biochem.Biophys.Res.Commun., 386:368-373, 2009 Cited by PubMed Abstract: tRNA identity elements assure the correct aminoacylation of tRNAs by the cognate aminoacyl-tRNA synthetases. tRNA(Ser) belongs to the so-called class II system, in which the identity elements are rather simple and are mostly located in the acceptor stem region, in contrast to 'class I', where tRNA determinants are more complex and are located within different regions of the tRNA. The structure of an Escherichia coli tRNA(Ser) acceptor stem microhelix was solved by high resolution X-ray structure analysis. The RNA crystallizes in the space group C2, with one molecule per asymmetric unit and with the cell constants a=35.79, b=39.13, c=31.37A, and beta=111.1 degrees . A defined hydration pattern of 97 water molecules surrounds the tRNA(Ser) acceptor stem microhelix. Additionally, two magnesium binding sites were detected in the tRNA(Ser) aminoacyl stem. PubMed: 19527687DOI: 10.1016/j.bbrc.2009.06.048 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.2 Å) |
Structure validation
Download full validation report






