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TitleDesign, synthesis, and in vitro biological evaluation of meta-sulfonamidobenzamide-based antibacterial LpxH inhibitors.
Journal, issue, pagesEur. J. Med. Chem., Vol. 278, Page 116790-116790, Year 2024
Publish dateMar 1, 2024 (structure data deposition date)
AuthorsBenediktsdottir, A. / Sooriyaarachchi, S. / Cao, S. / Ottosson, N.E. / Lindstrom, S. / Lundgren, B. / Kloditz, K. / Lola, D. / Bobileva, O. / Loza, E. ...Benediktsdottir, A. / Sooriyaarachchi, S. / Cao, S. / Ottosson, N.E. / Lindstrom, S. / Lundgren, B. / Kloditz, K. / Lola, D. / Bobileva, O. / Loza, E. / Hughes, D. / Jones, T.A. / Mowbray, S.L. / Zamaratski, E. / Sandstrom, A. / Karlen, A.
External linksEur. J. Med. Chem. / PubMed:39236497
MethodsX-ray diffraction
Resolution1.6 - 2.2 Å
Structure data

PDB-8s7f:
Crystal structure of Escherichia coli LpxH in complex with EBL-2805
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

PDB-9eng:
Structure of K.pneumoniae LpxH in complex with EBL-3218
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-MN:
Unknown entry

PDB-1h5p:
Solution structure of the human Sp100b SAND domain by heteronuclear NMR.

ChemComp-HOH:
WATER

PDB-1h55:
STRUCTURE OF HORSERADISH PEROXIDASE C1A COMPOUND II

Source
  • escherichia coli (E. coli)
  • klebsiella pneumoniae (bacteria)
KeywordsHYDROLASE / Lipid A biosynthesis pathway Endotoxin UDP-diacyl-glucosamine lipid X Gram-negative bacteria Antibiotic Inhibitor Lipopolysaccharides / Lipid A biosynthesis pathway Endotoxin UDP-diacyl-glucosamine lipid X Gram-negative bacteria Antibiotic Lipopolysaccharides

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