UniProt A0A5K1K7U1
20S proteasome beta-6 subunit (A0A5K1K7U1)
20S proteasome beta-6 subunit (UniProt A0A5K1K7U1), EC 3.4.25.1: 5 experimental structures on GenesisL1, 3 ligands bound, 11 pockets. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- A0A5K1K7U1
- Protein
- 20S proteasome beta-6 subunit
- EC
- 3.4.25.1
- Experimental structures
- 5
- Predicted models
- 0
- Ligands
- 3
- Pockets
- 11 · 2 records with a druggable one
Structures
5 records of A0A5K1K7U1 in the MolNFT archive: 5 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 7LXT | Structure of Plasmodium falciparum 20S proteasome with bound bortezomib | electron microscopy | M, a | BO2 | 5 (best 0.79) |
| 7LXT | Structure of plasmodium falciparum 20S proteasome with bound bortezomib | electron microscopy | M, a | BO2 | — |
| 7LXU | Structure of Plasmodium falciparum 20S proteasome with bound MPI-5 | electron microscopy | M, a | YHD | — |
| 7LXU | Structure of plasmodium falciparum 20S proteasome with bound mpi-5 | electron microscopy | M, a | YHD | — |
| 8W2F | Plasmodium falciparum 20S proteasome bound to an inhibitor | electron microscopy | M, a | A1AE6 | 6 (best 0.78) |
Ligands
- BO2 · N-[(1R)-1-(dihydroxyboryl)-3-methylbutyl]-N-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide · in 2 records
- YHD · N-[(1R)-2-([1,1'-biphenyl]-4-yl)-1-boronoethyl]-1-methyl-L-prolinamide · in 2 records
- A1AE6 · (3S)-1-[(2-fluoroethoxy)acetyl]-N-{[(4P)-4-(6-methylpyridin-3-yl)-1,3-thiazol-2-yl]methyl}piperidine-3-carboxamide · in 1 record
Elsewhere
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