3U7L
Crystal structures of the Staphylococcus aureus peptide deformylase in complex with two classes of new inhibitors
Summary for 3U7L
Entry DOI | 10.2210/pdb3u7l/pdb |
Related | 3U7K 3U7M 3U7N |
Descriptor | Peptide deformylase, ZINC ION, (S)-N-(cyclopentylmethyl)-2-(3-(3,5-difluorophenyl)ureido)-N-(2-(hydroxyamino)-2-oxoethyl)-3,3-dimethylbutanamide, ... (4 entities in total) |
Functional Keywords | pdf-inhibitor, pdf, peptide deformylase, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Staphylococcus aureus |
Total number of polymer chains | 1 |
Total formula weight | 22198.61 |
Authors | Lee, S.J.,Lee, S.-J.,Lee, S.K.,Yoon, H.-J.,Lee, H.H.,Kim, K.K.,Lee, B.J.,Suh, S.W. (deposition date: 2011-10-14, release date: 2012-06-27, Last modification date: 2023-11-01) |
Primary citation | Lee, S.J.,Lee, S.-J.,Lee, S.K.,Yoon, H.-J.,Lee, H.H.,Kim, K.K.,Lee, B.J.,Lee, B.I.,Suh, S.W. Structures of Staphylococcus aureus peptide deformylase in complex with two classes of new inhibitors Acta Crystallogr.,Sect.D, 68:784-793, 2012 Cited by PubMed: 22751663DOI: 10.1107/S0907444912011912 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.01 Å) |
Structure validation
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