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4J09

Crystal Structure of LpxA bound to RJPXD33

Summary for 4J09
Entry DOI10.2210/pdb4j09/pdb
DescriptorAcyl-[acyl-carrier-protein]--UDP-N-acetylglucosamine O-acyltransferase, Putative metabolite transport protein YjhB, PHOSPHATE ION, ... (6 entities in total)
Functional Keywordsacyltransferase, left-handed beta helix, transferase
Biological sourceEscherichia coli
More
Cellular locationCytoplasm: P0A722
Cell inner membrane; Multi-pass membrane protein (Potential): P39352
Total number of polymer chains2
Total formula weight29358.11
Authors
Jenkins, R.J.,Meagher, J.L.,Stuckey, J.A.,Dotson, G.D. (deposition date: 2013-01-30, release date: 2014-04-23, Last modification date: 2024-02-28)
Primary citationJenkins, R.J.,Heslip, K.A.,Meagher, J.L.,Stuckey, J.A.,Dotson, G.D.
Structural Basis for the Recognition of Peptide RJPXD33 by Acyltransferases in Lipid A Biosynthesis.
J.Biol.Chem., 289:15527-15535, 2014
Cited by
PubMed Abstract: UDP-N-acetylglucosamine acyltransferase (LpxA) and UDP-3-O-(acyl)-glucosamine acyltransferase (LpxD) constitute the essential, early acyltransferases of lipid A biosynthesis. Recently, an antimicrobial peptide inhibitor, RJPXD33, was identified with dual affinity for LpxA and LpxD. To gain a fundamental understanding of the molecular basis of inhibitor binding, we determined the crystal structure of LpxA from Escherichia coli in complex with RJPXD33 at 1.9 Å resolutions. Our results suggest that the peptide binds in a unique modality that mimics (R)-β-hydroxyacyl pantetheine binding to LpxA and displays how the peptide binds exclusive of the native substrate, acyl-acyl carrier protein. Acyltransferase binding studies with photo-labile RJPXD33 probes and truncations of RJPXD33 validated the structure and provided fundamental insights for future design of small molecule inhibitors. Overlay of the LpxA-RJPXD33 structure with E. coli LpxD identified a complementary peptide binding pocket within LpxD and serves as a model for further biochemical characterization of RJPXD33 binding to LpxD.
PubMed: 24742680
DOI: 10.1074/jbc.M114.564278
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

237735

数据于2025-06-18公开中

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