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Structure paper

TitlePyrrolamide DNA gyrase inhibitors: Optimization of antibacterial activity and efficacy.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 7416-7420, Year 2011
Publish dateSep 15, 2011 (structure data deposition date)
AuthorsSherer, B.A. / Hull, K. / Green, O. / Basarab, G. / Hauck, S. / Hill, P. / Loch, J.T. / Mullen, G. / Bist, S. / Bryant, J. ...Sherer, B.A. / Hull, K. / Green, O. / Basarab, G. / Hauck, S. / Hill, P. / Loch, J.T. / Mullen, G. / Bist, S. / Bryant, J. / Boriack-Sjodin, A. / Read, J. / Degrace, N. / Uria-Nickelsen, M. / Illingworth, R.N. / Eakin, A.E.
External linksBioorg. Med. Chem. Lett. / PubMed:22041057
MethodsX-ray diffraction
Resolution1.63 Å
Structure data

PDB-3ttz:
Crystal structure of a topoisomerase ATPase inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.63 Å

Chemicals

ChemComp-07N:
2-[(3S,4R)-4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}-3-fluoropiperidin-1-yl]-1,3-thiazole-5-carboxylic acid

ChemComp-MG:
Unknown entry

ChemComp-HOH:
WATER

Source
  • staphylococcus aureus (bacteria)
KeywordsISOMERASE/ISOMERASE INHIBITOR / protein-inhibitor complex / ATP-binding / structure-based drug design / antimicrobial / ISOMERASE-ISOMERASE INHIBITOR complex

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