7CI6
Crystal structure of P.aeruginosa LpxC in complex with inhibitor
Summary for 7CI6
Entry DOI | 10.2210/pdb7ci6/pdb |
Descriptor | UDP-3-O-acyl-N-acetylglucosamine deacetylase, (1S)-1-[1-[3-(4-chlorophenyl)propyl]imidazol-2-yl]ethanol, ZINC ION, ... (5 entities in total) |
Functional Keywords | udp-3-o-acyl-n-acetylglucosamine deacetylase, enva, lpxc, pseudomonas aeruginosa, hydrolase |
Biological source | Pseudomonas aeruginosa PAO1 |
Total number of polymer chains | 2 |
Total formula weight | 67024.46 |
Authors | Mima, M.,Baker, L.M.,Surgenor, A.,Robertson, A. (deposition date: 2020-07-07, release date: 2020-12-02, Last modification date: 2023-11-29) |
Primary citation | Yamada, Y.,Takashima, H.,Walmsley, D.L.,Ushiyama, F.,Matsuda, Y.,Kanazawa, H.,Yamaguchi-Sasaki, T.,Tanaka-Yamamoto, N.,Yamagishi, J.,Kurimoto-Tsuruta, R.,Ogata, Y.,Ohtake, N.,Angove, H.,Baker, L.,Harris, R.,Macias, A.,Robertson, A.,Surgenor, A.,Watanabe, H.,Nakano, K.,Mima, M.,Iwamoto, K.,Okada, A.,Takata, I.,Hitaka, K.,Tanaka, A.,Fujita, K.,Sugiyama, H.,Hubbard, R.E. Fragment-Based Discovery of Novel Non-Hydroxamate LpxC Inhibitors with Antibacterial Activity. J.Med.Chem., 63:14805-14820, 2020 Cited by PubMed: 33210531DOI: 10.1021/acs.jmedchem.0c01215 PDB entries with the same primary citation |
Experimental method |
Structure validation
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