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5CDM

2.5A structure of QPT-1 with S.aureus DNA gyrase and DNA

Summary for 5CDM
Entry DOI10.2210/pdb5cdm/pdb
DescriptorDNA gyrase subunit B,DNA gyrase subunit B, THYMIDINE-5'-MONOPHOSPHATE, DNA gyrase subunit A, ... (11 entities in total)
Functional Keywordstype iia topoisomerase, antibacterial, inhibitor, isomerase
Biological sourceStaphylococcus aureus
More
Cellular locationCytoplasm : P66937 Q99XG5
Total number of polymer chains8
Total formula weight165913.28
Authors
Bax, B.D.,Srikannathasan, V.,Chan, P.F. (deposition date: 2015-07-04, release date: 2015-12-16, Last modification date: 2024-01-10)
Primary citationChan, P.F.,Srikannathasan, V.,Huang, J.,Cui, H.,Fosberry, A.P.,Gu, M.,Hann, M.M.,Hibbs, M.,Homes, P.,Ingraham, K.,Pizzollo, J.,Shen, C.,Shillings, A.J.,Spitzfaden, C.E.,Tanner, R.,Theobald, A.J.,Stavenger, R.A.,Bax, B.D.,Gwynn, M.N.
Structural basis of DNA gyrase inhibition by antibacterial QPT-1, anticancer drug etoposide and moxifloxacin.
Nat Commun, 6:10048-10048, 2015
Cited by
PubMed: 26640131
DOI: 10.1038/ncomms10048
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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