6FTB
Staphylococcus aureus monofunctional glycosyltransferase in complex with moenomycin
Summary for 6FTB
Entry DOI | 10.2210/pdb6ftb/pdb |
Related | 2C6W 2OLU 2OLV 2ZC5 3DWK 3HZS |
Descriptor | Monofunctional glycosyltransferase, MOENOMYCIN, 1,2-ETHANEDIOL, ... (6 entities in total) |
Functional Keywords | transglycosylase, peptidoglycan, monofunctional, moenomycin, inhibitor, membrane, cell shape, cell wall biosynthesis, glycosyltransferase, peptidoglycan synthesis, transferase, antibiotics |
Biological source | Staphylococcus aureus MW2 |
Total number of polymer chains | 1 |
Total formula weight | 30092.58 |
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 citation | Punekar, 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: 30046666DOI: 10.1016/j.tcsw.2018.06.002 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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