6EE3
X-ray crystal structure of Pf-M1 in complex with inhibitor (6k) and catalytic zinc ion
Summary for 6EE3
Entry DOI | 10.2210/pdb6ee3/pdb |
Descriptor | M1 family aminopeptidase, ZINC ION, (1R,2r,3S,5R,7R)-N-[(1R)-2-(hydroxyamino)-2-oxo-1-(3',4',5'-trifluoro[1,1'-biphenyl]-4-yl)ethyl]tricyclo[3.3.1.1~3,7~]decane-2-carboxamide, ... (7 entities in total) |
Functional Keywords | m1 alanyl-aminopeptidase, protease, inhibitor, hydroxamic acid, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Plasmodium falciparum (isolate FcB1 / Columbia) |
Total number of polymer chains | 1 |
Total formula weight | 104531.87 |
Authors | Drinkwater, N.,McGowan, S. (deposition date: 2018-08-13, release date: 2018-12-26, Last modification date: 2024-03-13) |
Primary citation | Vinh, N.B.,Drinkwater, N.,Malcolm, T.R.,Kassiou, M.,Lucantoni, L.,Grin, P.M.,Butler, G.S.,Duffy, S.,Overall, C.M.,Avery, V.M.,Scammells, P.J.,McGowan, S. Hydroxamic Acid Inhibitors Provide Cross-Species Inhibition of Plasmodium M1 and M17 Aminopeptidases. J. Med. Chem., 62:622-640, 2019 Cited by PubMed: 30537832DOI: 10.1021/acs.jmedchem.8b01310 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.82 Å) |
Structure validation
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