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Structure paper

TitlePotent DNA gyrase inhibitors bind asymmetrically to their target using symmetrical bifurcated halogen bonds.
Journal, issue, pagesNat Commun, Vol. 12, Page 150-150, Year 2021
Publish dateMay 13, 2020 (structure data deposition date)
AuthorsKolaric, A. / Germe, T. / Hrast, M. / Stevenson, C.E.M. / Lawson, D.M. / Burton, N.P. / Voros, J. / Maxwell, A. / Minovski, N. / Anderluh, M.
External linksNat Commun / PubMed:33420011
MethodsX-ray diffraction
Resolution2.3 Å
Structure data

PDB-6z1a:
Ternary complex of Staphylococcus aureus DNA gyrase with AMK12 and DNA
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

Chemicals

ChemComp-EPE:
4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID / pH buffer*YM

ChemComp-MN:
Unknown entry

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-CL:
Unknown entry

ChemComp-Q52:
~{N}-[(4-chlorophenyl)methyl]-1-[2-(6-methoxy-1,5-naphthyridin-4-yl)ethyl]piperidin-4-amine

ChemComp-HOH:
WATER

Source
  • staphylococcus aureus (bacteria)
  • staphylococcus aureus subsp. aureus n315 (bacteria)
KeywordsISOMERASE / TYPE IIA TOPOISOMERASE / ANTIBACTERIAL / INHIBITOR / FUSION PROTEIN

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