2JRC
Solution structure of Peptidyl-tRNA Hydrolase from Mycobacterium tuberculosis H37Rv.
Summary for 2JRC
| Entry DOI | 10.2210/pdb2jrc/pdb |
| Descriptor | Peptidyl-tRNA hydrolase (1 entity in total) |
| Functional Keywords | pth, solution structure, mycobacterium tuberculosis h37rv, hydrolase |
| Biological source | Mycobacterium tuberculosis |
| Cellular location | Cytoplasm (By similarity): P65865 |
| Total number of polymer chains | 1 |
| Total formula weight | 22012.26 |
| Authors | Pulavarti, S.V.S.R.K.,Jain, A.,Pathak, P.P.,Arora, A. (deposition date: 2007-06-22, release date: 2008-05-27, Last modification date: 2023-12-20) |
| Primary citation | Pulavarti, S.V.,Jain, A.,Pathak, P.P.,Mahmood, A.,Arora, A. Solution structure and dynamics of peptidyl-tRNA hydrolase from Mycobacterium tuberculosis H37Rv. J.Mol.Biol., 378:165-177, 2008 Cited by PubMed Abstract: Eubacterial peptidyl-tRNA hydrolase is an essential enzyme that hydrolyzes peptidyl-tRNAs that are released into the cytoplasm because of premature termination of translation, expression of minigenes, and action of lincosamide and macrolide antibiotics. This averts the arrest of protein synthesis caused by depletion of free tRNA. Recently, we demonstrated that Mycobacterium tuberculosis peptidyl-tRNA hydrolase (MtPth) is present in the cytosol of mycobacterium and is capable of hydrolyzing peptidyl-tRNA. Here, we present the solution structure of MtPth, which is the first solution structure for this family of proteins. MtPth typically consists of seven-stranded mixed beta-sheet surrounded by six alpha-helices. The backbone dynamics for this enzyme were probed by measuring (15)N relaxation parameters and these were analyzed with model-free formalism and reduced spectral density mapping analysis. Overall, the protein molecule has tau(m) of 9.67+/-0.02 ns. The (15)N relaxation data analysis reveals that while majority of the protein backbone is rigid to motions, a short segment consisting of enzymatically critical residue H22, the loop-helix cover over the active site crevice, and the C-terminal helical hairpin exhibit motions on the milli-to microsecond timescale, all of which are linked to interaction with the substrate peptidyl-tRNA. PubMed: 18342886DOI: 10.1016/j.jmb.2008.02.027 PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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