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Structure paper

TitleSynthesis, Structure, and Antibiotic Activity of Aryl-Substituted LpxC Inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 56, Page 6954-6966, Year 2013
Publish dateJun 21, 2013 (structure data deposition date)
AuthorsLiang, X. / Lee, C.J. / Zhao, J. / Toone, E.J. / Zhou, P.
External linksJ. Med. Chem. / PubMed:23914798
MethodsX-ray diffraction
Resolution1.568 - 1.599 Å
Structure data

PDB-4lcf:
Crystal structure of the Pseudomonas aeruginosa LPXC/LPC-014 complex
Method: X-RAY DIFFRACTION / Resolution: 1.599 Å

PDB-4lcg:
Crystal structure of the Pseudomonas aeruginosa LPXC/LPC-050 complex
Method: X-RAY DIFFRACTION / Resolution: 1.568 Å

PDB-4lch:
Crystal structure of the Pseudomonas aeruginosa LPXC/LPC-051 complex
Method: X-RAY DIFFRACTION / Resolution: 1.596 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-1WL:
Nalpha-{4-[4-(4-aminophenyl)buta-1,3-diyn-1-yl]benzoyl}-N-hydroxy-L-histidinamide

ChemComp-NO3:
NITRATE ION

ChemComp-HOH:
WATER

ChemComp-1WM:
(betaS)-Nalpha-{4-[4-(4-aminophenyl)buta-1,3-diyn-1-yl]benzoyl}-N,beta-dihydroxy-L-tyrosinamide

ChemComp-1WN:
(betaS)-Nalpha-{4-[4-(4-aminophenyl)buta-1,3-diyn-1-yl]benzoyl}-N,beta-dihydroxy-beta-methyl-L-tyrosinamide

Source
  • pseudomonas aeruginosa (bacteria)
KeywordsHYDROLASE/ANTIBIOTIC / lipid A biosynthesis / lipid A synthesis / BAAB sandwich / LPXC / deacetylation / acyl UDP-GLCNAC / hydroxamate / HYDROLASE-ANTIBIOTIC complex

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