5DVP
Crystal structure of Mycobacterium tuberculosis L,D-transpeptidase 2 with Doripenem adduct
Summary for 5DVP
| Entry DOI | 10.2210/pdb5dvp/pdb |
| Related | 5DU7 5DUJ 5DVQ |
| Descriptor | L,D-transpeptidase 2, (2S,3R,4S)-2-[(2S,3R)-3-hydroxy-1-oxobutan-2-yl]-3-methyl-4-({(3S,5S)-5-[(sulfamoylamino)methyl]pyrrolidin-3-yl}sulfanyl)-3,4-dihydro-2H-pyrrole-5-carboxylic acid, SULFATE ION, ... (5 entities in total) |
| Functional Keywords | peptidoglycan synthesis enzyme, cell wall enzyme, transferase |
| Biological source | Mycobacterium tuberculosis |
| Cellular location | Cell membrane ; Lipid-anchor : I6Y9J2 |
| Total number of polymer chains | 2 |
| Total formula weight | 76178.38 |
| Authors | Kumar, P.,Lamichhane, G. (deposition date: 2015-09-21, release date: 2016-09-28, Last modification date: 2024-10-09) |
| Primary citation | Kumar, P.,Kaushik, A.,Lloyd, E.P.,Li, S.G.,Mattoo, R.,Ammerman, N.C.,Bell, D.T.,Perryman, A.L.,Zandi, T.A.,Ekins, S.,Ginell, S.L.,Townsend, C.A.,Freundlich, J.S.,Lamichhane, G. Non-classical transpeptidases yield insight into new antibacterials. Nat. Chem. Biol., 13:54-61, 2017 Cited by PubMed Abstract: Bacterial survival requires an intact peptidoglycan layer, a three-dimensional exoskeleton that encapsulates the cytoplasmic membrane. Historically, the final steps of peptidoglycan synthesis are known to be carried out by D,D-transpeptidases, enzymes that are inhibited by the β-lactams, which constitute >50% of all antibacterials in clinical use. Here, we show that the carbapenem subclass of β-lactams are distinctly effective not only because they inhibit D,D-transpeptidases and are poor substrates for β-lactamases, but primarily because they also inhibit non-classical transpeptidases, namely the L,D-transpeptidases, which generate the majority of linkages in the peptidoglycan of mycobacteria. We have characterized the molecular mechanisms responsible for inhibition of L,D-transpeptidases of Mycobacterium tuberculosis and a range of bacteria including ESKAPE pathogens, and used this information to design, synthesize and test simplified carbapenems with potent antibacterial activity. PubMed: 27820797DOI: 10.1038/nchembio.2237 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.18 Å) |
Structure validation
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