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4WF9

The crystal structure of the large ribosomal subunit of Staphylococcus aureus in complex with telithromycin

Summary for 4WF9
Entry DOI10.2210/pdb4wf9/pdb
Related4WCE 4WFA 4WFB
Descriptor23S ribosomal RNA, 50S ribosomal protein L15, 50S ribosomal protein L16, ... (33 entities in total)
Functional Keywordsribosome, rna, bacteria
Biological sourceStaphylococcus aureus subsp. aureus NCTC 8325
More
Total number of polymer chains26
Total formula weight1349619.79
Authors
Eyal, Z.,Matzov, D.,Krupkin, M.,Wekselman, I.,Zimmerman, E.,Rozenberg, H.,Bashan, A.,Yonath, A.E. (deposition date: 2014-09-14, release date: 2015-10-21, Last modification date: 2024-01-10)
Primary citationEyal, Z.,Matzov, D.,Krupkin, M.,Wekselman, I.,Paukner, S.,Zimmerman, E.,Rozenberg, H.,Bashan, A.,Yonath, A.
Structural insights into species-specific features of the ribosome from the pathogen Staphylococcus aureus.
Proc.Natl.Acad.Sci.USA, 112:E5805-E5814, 2015
Cited by
PubMed Abstract: The emergence of bacterial multidrug resistance to antibiotics threatens to cause regression to the preantibiotic era. Here we present the crystal structure of the large ribosomal subunit from Staphylococcus aureus, a versatile Gram-positive aggressive pathogen, and its complexes with the known antibiotics linezolid and telithromycin, as well as with a new, highly potent pleuromutilin derivative, BC-3205. These crystal structures shed light on specific structural motifs of the S. aureus ribosome and the binding modes of the aforementioned antibiotics. Moreover, by analyzing the ribosome structure and comparing it with those of nonpathogenic bacterial models, we identified some unique internal and peripheral structural motifs that may be potential candidates for improving known antibiotics and for use in the design of selective antibiotic drugs against S. aureus.
PubMed: 26464510
DOI: 10.1073/pnas.1517952112
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.427 Å)
Structure validation

237992

數據於2025-06-25公開中

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