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6FTB

Staphylococcus aureus monofunctional glycosyltransferase in complex with moenomycin

Summary for 6FTB
Entry DOI10.2210/pdb6ftb/pdb
Related2C6W 2OLU 2OLV 2ZC5 3DWK 3HZS
DescriptorMonofunctional glycosyltransferase, MOENOMYCIN, 1,2-ETHANEDIOL, ... (6 entities in total)
Functional Keywordstransglycosylase, peptidoglycan, monofunctional, moenomycin, inhibitor, membrane, cell shape, cell wall biosynthesis, glycosyltransferase, peptidoglycan synthesis, transferase, antibiotics
Biological sourceStaphylococcus aureus MW2
Total number of polymer chains1
Total formula weight30092.58
Authors
Punekar, A.S.,Dowson, C.J.,Roper, D.I. (deposition date: 2018-02-20, release date: 2018-06-27, Last modification date: 2024-01-17)
Primary citationPunekar, A.S.,Samsudin, F.,Lloyd, A.J.,Dowson, C.G.,Scott, D.J.,Khalid, S.,Roper, D.I.
The role of the jaw subdomain of peptidoglycan glycosyltransferases for lipid II polymerization.
Cell Surf, 2:54-66, 2018
Cited by
PubMed Abstract: Bacterial peptidoglycan glycosyltransferases (PGT) catalyse the essential polymerization of lipid II into linear glycan chains required for peptidoglycan biosynthesis. The PGT domain is composed of a large head subdomain and a smaller jaw subdomain and can be potently inhibited by the antibiotic moenomycin A (MoeA). We present an X-ray structure of the MoeA-bound monofunctional PGT enzyme, revealing electron density for a second MoeA bound to the jaw subdomain as well as the PGT donor site. Isothermal titration calorimetry confirms two drug-binding sites with markedly different affinities and positive cooperativity. Hydrophobic cluster analysis suggests that the membrane-interacting surface of the jaw subdomain has structural and physicochemical properties similar to amphipathic cationic -helical antimicrobial peptides for lipid II recognition and binding. Furthermore, molecular dynamics simulations of the drug-free and -bound forms of the enzyme demonstrate the importance of the jaw subdomain movement for lipid II selection and polymerization process and provide molecular-level insights into the mechanism of peptidoglycan biosynthesis by PGTs.
PubMed: 30046666
DOI: 10.1016/j.tcsw.2018.06.002
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

227111

數據於2024-11-06公開中

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