2IRX
Crystal Structure of the Polymerase Domain from Mycobacterium tuberculosis Ligase D with GTP and Manganese.
Summary for 2IRX
Entry DOI | 10.2210/pdb2irx/pdb |
Related | 2IRU 2IRY |
Descriptor | DNA ligase-like protein Rv0938/MT0965, MANGANESE (II) ION, GUANOSINE-5'-TRIPHOSPHATE, ... (4 entities in total) |
Functional Keywords | polymerase, primase, ligase, nhej, gtp, transferase |
Biological source | Mycobacterium tuberculosis |
Total number of polymer chains | 1 |
Total formula weight | 33403.27 |
Authors | Brissett, N.C.,Pitcher, R.S.,Doherty, A.J. (deposition date: 2006-10-16, release date: 2007-01-02, Last modification date: 2024-02-21) |
Primary citation | Pitcher, R.S.,Brissett, N.C.,Picher, A.J.,Andrade, P.,Juarez, R.,Thompson, D.,Fox, G.C.,Blanco, L.,Doherty, A.J. Structure and function of a mycobacterial NHEJ DNA repair polymerase. J.Mol.Biol., 366:391-405, 2007 Cited by PubMed Abstract: Non homologous end-joining (NHEJ)-mediated repair of DNA double-strand breaks in prokaryotes requires Ku and a specific multidomain DNA ligase (LigD). We present crystal structures of the primase/polymerisation domain (PolDom) of Mycobacterium tuberculosis LigD, alone and complexed with nucleotides. The PolDom structure combines the general fold of the archaeo-eukaryotic primase (AEP) superfamily with additional loops and domains that together form a deep cleft on the surface, likely used for DNA binding. Enzymatic analysis indicates that the PolDom of LigD, even in the absence of accessory domains and Ku proteins, has the potential to recognise DNA end-joining intermediates. Strikingly, one of the main signals for the specific and efficient binding of PolDom to DNA is the presence of a 5'-phosphate group, located at the single/double-stranded junction at both gapped and 3'-protruding DNA molecules. Although structurally unrelated, Pol lambda and Pol mu, the two eukaryotic DNA polymerases involved in NHEJ, are endowed with a similar capacity to bind a 5'-phosphate group. Other properties that are beneficial for NHEJ, such as the ability to generate template distortions and realignments of the primer, displayed by Pol lambda and Pol mu, are shared by the PolDom of bacterial LigD. In addition, PolDom can perform non-mutagenic translesion synthesis on termini containing modified bases. Significantly, ribonucleotide insertion appears to be a recurrent theme associated with NHEJ, maximised in this case by the deployment of a dedicated primase, although its in vivo relevance is unknown. PubMed: 17174332DOI: 10.1016/j.jmb.2006.10.046 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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