8G6E
Structure of the Plasmodium falciparum 20S proteasome complexed with inhibitor TDI-8304
Summary for 8G6E
Entry DOI | 10.2210/pdb8g6e/pdb |
Related | 8G6F 8UD9 |
EMDB information | 29764 |
Descriptor | Proteasome subunit alpha type-6, Proteasome subunit beta, (7S,10S,13S)-N-cyclopentyl-10-[2-(morpholin-4-yl)ethyl]-9,12-dioxo-13-(2-oxopyrrolidin-1-yl)-2-oxa-8,11-diazabicyclo[13.3.1]nonadeca-1(19),15,17-triene-7-carboxamide, ... (16 entities in total) |
Functional Keywords | proteasome, inhibitor, 20s, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Plasmodium falciparum NF54 More |
Total number of polymer chains | 28 |
Total formula weight | 766218.55 |
Authors | Hsu, H.-C.,Li, H. (deposition date: 2023-02-15, release date: 2023-12-20, Last modification date: 2024-01-03) |
Primary citation | Hsu, H.C.,Li, D.,Zhan, W.,Ye, J.,Liu, Y.J.,Leung, A.,Qin, J.,Crespo, B.,Gamo, F.J.,Zhang, H.,Cui, L.,Roth, A.,Kirkman, L.A.,Li, H.,Lin, G. Structures revealing mechanisms of resistance and collateral sensitivity of Plasmodium falciparum to proteasome inhibitors. Nat Commun, 14:8302-8302, 2023 Cited by PubMed: 38097652DOI: 10.1038/s41467-023-44077-2 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.18 Å) |
Structure validation
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