3IX4
LasR-TP1 complex
Summary for 3IX4
Entry DOI | 10.2210/pdb3ix4/pdb |
Related | 3IX3 3IX8 |
Descriptor | Transcriptional activator protein lasR, 2,4-dibromo-6-({[(2-nitrophenyl)carbonyl]amino}methyl)phenyl 2-chlorobenzoate (3 entities in total) |
Functional Keywords | quorum sensing, triphenyl mimic, activator, dna-binding, transcription, transcription regulation |
Biological source | Pseudomonas aeruginosa |
Total number of polymer chains | 8 |
Total formula weight | 159139.65 |
Authors | Zou, Y.,Nair, S.K. (deposition date: 2009-09-03, release date: 2009-09-15, Last modification date: 2023-09-06) |
Primary citation | Zou, Y.,Nair, S.K. Molecular basis for the recognition of structurally distinct autoinducer mimics by the Pseudomonas aeruginosa LasR quorum-sensing signaling receptor. Chem.Biol., 16:961-970, 2009 Cited by PubMed Abstract: The human pathogen Pseudomonas aeruginosa coordinates the expression of virulence factors using quorum sensing, a signaling cascade triggered by the activation of signal receptors by small-molecule autoinducers. These homoserine lactone autoinducers stabilize their cognate receptors and activate their functions as transcription factors. Because quorum sensing regulates the progression of infection and host immune resistance, significant efforts have been devoted toward the identification of small molecules that disrupt this process. Screening efforts have identified a class of triphenyl compounds that are structurally distinct from the homoserine lactone autoinducer, yet interact specifically and potently with LasR receptor to modulate quorum sensing (Muh et al., 2006a). Here we present the high-resolution crystal structures of the ligand binding domain of LasR in complex with the autoinducer N-3-oxo-dodecanoyl homoserine lactone (1.4 A resolution), and with the triphenyl mimics TP-1, TP-3, and TP-4 (to between 1.8 A and 2.3 A resolution). These crystal structures provide a molecular rationale for understanding how chemically distinct compounds can be accommodated by a highly selective receptor, and provide the framework for the development of novel quorum-sensing regulators, utilizing the triphenyl scaffold. PubMed: 19778724DOI: 10.1016/j.chembiol.2009.09.001 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
Download full validation report