5X22
Crystal structure of Thermus thermophilus transcription initiation complex with GpA and CMPcPP
Summary for 5X22
| Entry DOI | 10.2210/pdb5x22/pdb |
| Related | 5X21 |
| Descriptor | DNA-directed RNA polymerase subunit alpha, ZINC ION, 5'-O-[(S)-hydroxy{[(S)-hydroxy(phosphonooxy)phosphoryl]methyl}phosphoryl]cytidine, ... (11 entities in total) |
| Functional Keywords | transcription, rna polymerase, primer-dependent initiation, transferase-dna complex, transferase/dna |
| Biological source | Thermus thermophilus More |
| Total number of polymer chains | 18 |
| Total formula weight | 890215.67 |
| Authors | Zhang, Y.,Ebright, R. (deposition date: 2017-01-29, release date: 2017-07-05, Last modification date: 2024-11-20) |
| Primary citation | Maffioli, S.I.,Zhang, Y.,Degen, D.,Carzaniga, T.,Del Gatto, G.,Serina, S.,Monciardini, P.,Mazzetti, C.,Guglierame, P.,Candiani, G.,Chiriac, A.I.,Facchetti, G.,Kaltofen, P.,Sahl, H.G.,Deho, G.,Donadio, S.,Ebright, R.H. Antibacterial Nucleoside-Analog Inhibitor of Bacterial RNA Polymerase. Cell, 169:1240-1248.e23, 2017 Cited by PubMed Abstract: Drug-resistant bacterial pathogens pose an urgent public-health crisis. Here, we report the discovery, from microbial-extract screening, of a nucleoside-analog inhibitor that inhibits bacterial RNA polymerase (RNAP) and exhibits antibacterial activity against drug-resistant bacterial pathogens: pseudouridimycin (PUM). PUM is a natural product comprising a formamidinylated, N-hydroxylated Gly-Gln dipeptide conjugated to 6'-amino-pseudouridine. PUM potently and selectively inhibits bacterial RNAP in vitro, inhibits bacterial growth in culture, and clears infection in a mouse model of Streptococcus pyogenes peritonitis. PUM inhibits RNAP through a binding site on RNAP (the NTP addition site) and mechanism (competition with UTP for occupancy of the NTP addition site) that differ from those of the RNAP inhibitor and current antibacterial drug rifampin (Rif). PUM exhibits additive antibacterial activity when co-administered with Rif, exhibits no cross-resistance with Rif, and exhibits a spontaneous resistance rate an order-of-magnitude lower than that of Rif. PUM is a highly promising lead for antibacterial therapy. PubMed: 28622509DOI: 10.1016/j.cell.2017.05.042 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.35 Å) |
Structure validation
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