UniProt Q8I0U7
20S proteasome beta-1 subunit (Q8I0U7)
20S proteasome beta-1 subunit (UniProt Q8I0U7), EC 3.4.25.1: 13 experimental structures on GenesisL1, 1 ligand bound, 28 pockets. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- Q8I0U7
- Protein
- 20S proteasome beta-1 subunit
- EC
- 3.4.25.1
- Experimental structures
- 13
- Predicted models
- 0
- Ligands
- 1
- Pockets
- 28 · 5 records with a druggable one
Structures
13 records of Q8I0U7 in the MolNFT archive: 13 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 5FMG | Structure and function based design of Plasmodium-selective proteasome inhibitors | electron microscopy | H, V | — | 6 (best 0.77) |
| 5FMG | Structure and function based design of plasmodium-selective proteasome inhibitors | electron microscopy | H, V | — | — |
| 6MUV | The structure of the Plasmodium falciparum 20S proteasome in complex with two PA28 activators | electron microscopy | H, V | — | — |
| 6MUV | The structure of the plasmodium falciparum 20S proteasome in complex with two PA28 activators | electron microscopy | H, V | — | — |
| 6MUW | The structure of the Plasmodium falciparum 20S proteasome. | electron microscopy | H, V | — | 6 (best 0.84) |
| 6MUW | The structure of the plasmodium falciparum 20S proteasome. | electron microscopy | H, V | — | — |
| 6MUX | The structure of the Plasmodium falciparum 20S proteasome in complex with one PA28 activator | electron microscopy | H, V | — | 5 (best 0.80) |
| 6MUX | The structure of the plasmodium falciparum 20S proteasome in complex with one PA28 activator | electron microscopy | H, V | — | — |
| 7LXT | Structure of Plasmodium falciparum 20S proteasome with bound bortezomib | electron microscopy | H, V | BO2 | 6 (best 0.80) |
| 7LXT | Structure of plasmodium falciparum 20S proteasome with bound bortezomib | electron microscopy | H, V | BO2 | — |
| 7LXU | Structure of Plasmodium falciparum 20S proteasome with bound MPI-5 | electron microscopy | H, V | — | — |
| 7LXU | Structure of plasmodium falciparum 20S proteasome with bound mpi-5 | electron microscopy | H, V | — | — |
| 8W2F | Plasmodium falciparum 20S proteasome bound to an inhibitor | electron microscopy | H, V | — | 5 (best 0.81) |
Ligands
- BO2 · N-[(1R)-1-(dihydroxyboryl)-3-methylbutyl]-N-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide · in 2 records
Elsewhere
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