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Structure paper

TitleMethicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as a target for bis-indole alkaloids with antibacterial activities.
Journal, issue, pagesJ. Biol. Chem., Vol. 286, Page 44716-44725, Year 2011
Publish dateJul 19, 2011 (structure data deposition date)
AuthorsZoraghi, R. / Worrall, L. / See, R.H. / Strangman, W. / Popplewell, W.L. / Gong, H. / Samaai, T. / Swayze, R.D. / Kaur, S. / Vuckovic, M. ...Zoraghi, R. / Worrall, L. / See, R.H. / Strangman, W. / Popplewell, W.L. / Gong, H. / Samaai, T. / Swayze, R.D. / Kaur, S. / Vuckovic, M. / Finlay, B.B. / Brunham, R.C. / McMaster, W.R. / Davies-Coleman, M.T. / Strynadka, N.C. / Andersen, R.J. / Reiner, N.E.
External linksJ. Biol. Chem. / PubMed:22030393
MethodsX-ray diffraction
Resolution3.05 - 3.3 Å
Structure data

PDB-3t05:
Crystal structure of S. aureus Pyruvate Kinase
Method: X-RAY DIFFRACTION / Resolution: 3.05 Å

PDB-3t07:
Crystal structure of S. aureus Pyruvate Kinase in complex with a naturally occurring bis-indole alkaloid
Method: X-RAY DIFFRACTION / Resolution: 3.3 Å

Chemicals

ChemComp-PO4:
PHOSPHATE ION

ChemComp-09C:
(3S,5R)-3,5-bis(6-bromo-1H-indol-3-yl)piperazin-2-one

Source
  • staphylococcus aureus subsp. aureus (bacteria)
KeywordsTRANSFERASE / tetramer / glycolysis / TRANSFERASE/TRANSFERASE INHIBITOR / ligand / TRANSFERASE-TRANSFERASE INHIBITOR complex

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