5VFX
Structure of an accessory protein of the pCW3 relaxosome in complex with the origin of transfer (oriT) DNA
Summary for 5VFX
Entry DOI | 10.2210/pdb5vfx/pdb |
Related | 5VFY |
Descriptor | TcpK, oriT, ... (4 entities in total) |
Functional Keywords | conjugation, winged helix-turn-helix, orit, clostridium perfringens, dna binding protein-dna complex, dna binding protein/dna |
Biological source | Clostridium perfringens More |
Total number of polymer chains | 16 |
Total formula weight | 160513.05 |
Authors | Traore, D.A.K.,Wisniewski, J.A.,Flanigan, S.F.,Conroy, P.J.,Panjikar, S.,Mok, Y.-F.,Lao, C.,Griffin, M.D.W.,Adams, V.,Rood, J.I.,Whisstock, J.C. (deposition date: 2017-04-10, release date: 2018-04-18, Last modification date: 2023-10-04) |
Primary citation | Traore, D.A.K.,Wisniewski, J.A.,Flanigan, S.F.,Conroy, P.J.,Panjikar, S.,Mok, Y.F.,Lao, C.,Griffin, M.D.W.,Adams, V.,Rood, J.I.,Whisstock, J.C. Crystal structure of TcpK in complex with oriT DNA of the antibiotic resistance plasmid pCW3. Nat Commun, 9:3732-3732, 2018 Cited by PubMed Abstract: Conjugation is fundamental for the acquisition of new genetic traits and the development of antibiotic resistance in pathogenic organisms. Here, we show that a hypothetical Clostridium perfringens protein, TcpK, which is encoded by the tetracycline resistance plasmid pCW3, is essential for efficient conjugative DNA transfer. Our studies reveal that TcpK is a member of the winged helix-turn-helix (wHTH) transcription factor superfamily and that it forms a dimer in solution. Furthermore, TcpK specifically binds to a nine-nucleotide sequence that is present as tandem repeats within the pCW3 origin of transfer (oriT). The X-ray crystal structure of the TcpK-TcpK box complex reveals a binding mode centered on and around the β-wing, which is different from what has been previously shown for other wHTH proteins. Structure-guided mutagenesis experiments validate the specific interaction between TcpK and the DNA molecule. Additional studies highlight that the TcpK dimer is important for specific DNA binding. PubMed: 30213934DOI: 10.1038/s41467-018-06096-2 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.81 Å) |
Structure validation
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