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8G6E

Structure of the Plasmodium falciparum 20S proteasome complexed with inhibitor TDI-8304

Summary for 8G6E
Entry DOI10.2210/pdb8g6e/pdb
Related8G6F 8UD9
EMDB information29764
DescriptorProteasome 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 Keywordsproteasome, inhibitor, 20s, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourcePlasmodium falciparum NF54
More
Total number of polymer chains28
Total formula weight766218.55
Authors
Hsu, H.-C.,Li, H. (deposition date: 2023-02-15, release date: 2023-12-20, Last modification date: 2024-01-03)
Primary citationHsu, 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: 38097652
DOI: 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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