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Structure paper

TitleExploring the UDP pocket of LpxC through amino acid analogs.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 23, Page 2362-2367, Year 2013
Publish dateFeb 5, 2013 (structure data deposition date)
AuthorsHale, M.R. / Hill, P. / Lahiri, S. / Miller, M.D. / Ross, P. / Alm, R. / Gao, N. / Kutschke, A. / Johnstone, M. / Prince, B. ...Hale, M.R. / Hill, P. / Lahiri, S. / Miller, M.D. / Ross, P. / Alm, R. / Gao, N. / Kutschke, A. / Johnstone, M. / Prince, B. / Thresher, J. / Yang, W.
External linksBioorg. Med. Chem. Lett. / PubMed:23499237
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-4j3d:
Pseudomonas aeruginosa LpxC in complex with a hydroxamate inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-1JS:
N~1~-hydroxy-N~5~-(3-hydroxypropyl)-N~2~-[4-(phenylethynyl)benzoyl]-L-glutamamide

ChemComp-HOH:
WATER

Source
  • pseudomonas aeruginosa (bacteria)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / LpxC / metalloamidase / UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase / HYDROLASE-HYDROLASE INHIBITOR complex

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