6X27
Lon protease proteolytic domain complexed with bortezomib
Summary for 6X27
Entry DOI | 10.2210/pdb6x27/pdb |
Related | 6WYS 6WZV 6X1M |
Descriptor | Lon protease homolog, mitochondrial, N-[(1R)-1-(DIHYDROXYBORYL)-3-METHYLBUTYL]-N-(PYRAZIN-2-YLCARBONYL)-L-PHENYLALANINAMIDE, PENTAETHYLENE GLYCOL, ... (5 entities in total) |
Functional Keywords | covalent inhibitor, proteolytic domain, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 12 |
Total formula weight | 291683.35 |
Authors | Lee, C.C.,Spraggon, G. (deposition date: 2020-05-20, release date: 2021-04-14, Last modification date: 2023-10-18) |
Primary citation | Kingsley, L.J.,He, X.,McNeill, M.,Nelson, J.,Nikulin, V.,Ma, Z.,Lu, W.,Zhou, V.W.,Manuia, M.,Kreusch, A.,Gao, M.Y.,Witmer, D.,Vaillancourt, M.T.,Lu, M.,Greenblatt, S.,Lee, C.,Vashisht, A.,Bender, S.,Spraggon, G.,Michellys, P.Y.,Jia, Y.,Haling, J.R.,Lelais, G. Structure-Based Design of Selective LONP1 Inhibitors for Probing In Vitro Biology. J.Med.Chem., 64:4857-4869, 2021 Cited by PubMed: 33821636DOI: 10.1021/acs.jmedchem.0c02152 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.12 Å) |
Structure validation
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