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-Structure paper
Title | Increased hydrophobic interactions of iclaprim with Staphylococcus aureus dihydrofolate reductase are responsible for the increase in affinity and antibacterial activity |
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Journal, issue, pages | J. Antimicrob. Chemother., Vol. 63, Page 687-698, Year 2009 |
Publish date | Jan 8, 2009 (structure data deposition date) |
Authors | Oefner, C. / Bandera, M. / Haldimann, A. / Laue, H. / Schulz, H. / Mukhija, S. / Parisi, S. / Weiss, L. / Lociuro, S. / Dale, G.E. |
External links | J. Antimicrob. Chemother. / PubMed:19211577 |
Methods | X-ray diffraction |
Resolution | 2 - 2.35 Å |
Structure data | PDB-3fra: PDB-3frb: PDB-3frd: PDB-3fre: PDB-3frf: |
Chemicals | ChemComp-NAP: ChemComp-I2H: ChemComp-HOH: ChemComp-TOP: ChemComp-NDP: ChemComp-DHF: ChemComp-XCF: |
Source |
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Keywords | OXIDOREDUCTASE / DHFR / NADP / One-carbon metabolism / S. aureus DHFR / S aureus DHFR |