Literature DB >> 3118944

tRNA recognition site of Escherichia coli methionyl-tRNA synthetase.

O Leon1, L H Schulman.   

Abstract

We have previously shown that anticodon bases are essential for specific recognition of tRNA substrates by Escherichia coli methionyl-tRNA synthetase (MetRS) [Schulman, L. H., & Pelka, H. (1983) Proc. Natl. Acad. Sci. U.S.A. 80, 6755-6759] and that the enzyme tightly binds to C34 at the wobble position of E. coli initiator methionine tRNA (tRNAfMet) [Pelka, H., & Schulman, L. H. (1986) Biochemistry 25, 4450-4456]. We have also previously demonstrated that an affinity labeling derivative of tRNAfMet can be quantitatively cross-linked to the tRNA binding site of MetRS [Valenzuela, D., & Schulman, L. H. (1986) Biochemistry 25, 4555-4561]. Here, we have determined the site in MetRS which is cross-linked to the anticodon of tRNAfMet, as well as the location of four additional cross-links. Only a single peptide, containing Lys465, is covalently coupled to C34, indicating that the recognition site for the anticodon is close to this sequence in the three-dimensional structure of MetRS. The D loop at one corner of the tRNA molecule is cross-linked to three peptides, containing Lys402, Lys439, and Lys596. The 5' terminus of the tRNA is cross-linked to Lys640, near the carboxy terminus of the enzyme. Since the 3' end of tRNAfMet is positioned close to the active site in the N-terminal domain [Hountondji, C., Blanquet, S., & Lederer, F. (1985) Biochemistry 24, 1175-1180], this result indicates that the carboxy ends of the two polypeptide chains of native dimeric MetRS are folded back toward the N-terminal domain of each subunit.

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Year:  1987        PMID: 3118944     DOI: 10.1021/bi00391a030

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  7 in total

1.  A study of communication pathways in methionyl- tRNA synthetase by molecular dynamics simulations and structure network analysis.

Authors:  Amit Ghosh; Saraswathi Vishveshwara
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-26       Impact factor: 11.205

2.  Selection of suppressor methionyl-tRNA synthetases: mapping the tRNA anticodon binding site.

Authors:  T Meinnel; Y Mechulam; D Le Corre; M Panvert; S Blanquet; G Fayat
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

3.  Activation of microhelix charging by localized helix destabilization.

Authors:  R W Alexander; B E Nordin; P Schimmel
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

4.  Peptides at the tRNA binding site of the crystallizable monomeric form of E. coli methionyl-tRNA synthetase.

Authors:  L H Schulman; H Pelka; O Leon
Journal:  Nucleic Acids Res       Date:  1987-12-23       Impact factor: 16.971

5.  Structural similarities in glutaminyl- and methionyl-tRNA synthetases suggest a common overall orientation of tRNA binding.

Authors:  J J Perona; M A Rould; T A Steitz; J L Risler; C Zelwer; S Brunie
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

6.  Covalent methionylation of Escherichia coli methionyl-tRNA synthethase: identification of the labeled amino acid residues by matrix-assisted laser desorption-ionization mass spectrometry.

Authors:  S Gillet; C Hountondji; J M Schmitter; S Blanquet
Journal:  Protein Sci       Date:  1997-11       Impact factor: 6.725

7.  Aspartyl-tRNA synthetase from Escherichia coli: cloning and characterisation of the gene, homologies of its translated amino acid sequence with asparaginyl- and lysyl-tRNA synthetases.

Authors:  G Eriani; G Dirheimer; J Gangloff
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

  7 in total

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