Article (Scientific journals)
Crystal structures of complexes of bacterial DD-peptidases with peptidoglycan-mimetic ligands: the substrate specificity puzzle.
Sauvage, Eric; Powell, Ailsa J; Heilemann, Jason et al.
2008In Journal of Molecular Biology, 381 (2), p. 383-93
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Keywords :
Actinomycetales/enzymology; Arginine/chemistry/metabolism; Bacterial Proteins/chemistry/metabolism; Binding Sites; Crystallography, X-Ray/methods; Escherichia coli/enzymology; Models, Biological; Models, Molecular; Molecular Structure; Penicillin-Binding Proteins/chemistry/metabolism; Peptidoglycan/chemistry/metabolism; Protein Structure, Secondary; Serine-Type D-Ala-D-Ala Carboxypeptidase/chemistry/metabolism; Substrate Specificity; beta-Lactams/chemistry/metabolism
Abstract :
[en] The X-ray crystal structures of covalent complexes of the Actinomadura R39 dd-peptidase and Escherichia coli penicillin-binding protein (PBP) 5 with beta-lactams bearing peptidoglycan-mimetic side chains have been determined. The structure of the hydrolysis product of an analogous peptide bound noncovalently to the former enzyme has also been obtained. The R39 DD-peptidase structures reveal the presence of a specific binding site for the D-alpha-aminopimelyl side chain, characteristic of the stem peptide of Actinomadura R39. This binding site features a hydrophobic cleft for the pimelyl methylene groups and strong hydrogen bonding to the polar terminus. Both of these active site elements are provided by amino acid side chains from two separate domains of the protein. In contrast, no clear electron density corresponding to the terminus of the peptidoglycan-mimetic side chains is present when these beta-lactams are covalently bound to PBP5. There is, therefore, no indication of a specific side-chain binding site in this enzyme. These results are in agreement with those from kinetics studies published earlier and support the general prediction made at the time of a direct correlation between kinetics and structural evidence. The essential high-molecular-mass PBPs have demonstrated, to date, no specific reactivity with peptidoglycan-mimetic peptide substrates and beta-lactam inhibitors and, thus, probably do not possess a specific substrate-binding site of the type demonstrated here with the R39 DD-peptidase. This striking deficiency may represent a sophisticated defense mechanism against low-molecular-mass substrate-analogue inhibitors/antibiotics; its discovery should focus new inhibitor design.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Sauvage, Eric ;  Université de Liège - ULiège > Centre d'ingénierie des protéines
Powell, Ailsa J
Heilemann, Jason
Josephine, Helen R
Charlier, Paulette ;  Université de Liège - ULiège > Département des sciences de la vie > Cristallographie des macromolécules biologiques
Davies, Christopher
Pratt, R. F.
Language :
English
Title :
Crystal structures of complexes of bacterial DD-peptidases with peptidoglycan-mimetic ligands: the substrate specificity puzzle.
Publication date :
2008
Journal title :
Journal of Molecular Biology
ISSN :
0022-2836
eISSN :
1089-8638
Publisher :
Academic Press, London, United Kingdom
Volume :
381
Issue :
2
Pages :
383-93
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 28 November 2010

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