9FST
Yeast 20S proteasome with human beta1i (1-51) in complex with epoxyketone inhibitor LU-001i
This is a non-PDB format compatible entry.
Summary for 9FST
| Entry DOI | 10.2210/pdb9fst/pdb |
| Related | 5CZ4 |
| Descriptor | Proteasome subunit alpha type-2, Proteasome subunit beta type-4, Proteasome subunit beta type-5, ... (20 entities in total) |
| Functional Keywords | proteasome, mutant, human chimeric subunit, structure-based drug development, inhibitor, binding analysis, hydrolase |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 28 |
| Total formula weight | 734428.36 |
| Authors | Maurits, E.,Huber, E.M.,Dekker, P.M.,Wang, X.,Heinemeyer, W.,Florea, B.I.,Groll, M.,Overkleeft, H.S. (deposition date: 2024-06-21, release date: 2024-07-17, Last modification date: 2024-11-13) |
| Primary citation | Maurits, E.,Huber, E.M.,Dekker, P.M.,Wang, X.,Heinemeyer, W.,Florea, B.I.,Groll, M.,Overkleeft, H.S. Structure-based design of peptide epoxyketones selectively targeting the three human immunoproteasome active sites To Be Published, |
| Experimental method | X-RAY DIFFRACTION (2.75 Å) |
Structure validation
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