UniProt I7BFC3
Protease (I7BFC3)
Protease (UniProt I7BFC3): 8 experimental structures on GenesisL1, 3 ligands bound, 1 pocket. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- I7BFC3
- Protein
- Protease
- Experimental structures
- 8
- Predicted models
- 0
- Ligands
- 3
- Pockets
- 1 · 0 records with a druggable one
Structures
8 records of I7BFC3 in the MolNFT archive: 8 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 5T2E | Crystal Structure of multi-drug resistant HIV-1 protease PR-S17 | x-ray diffraction | A | CL | 1 (best 0.48) |
| 5T2E | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 | x-ray diffraction | A | CL | — |
| 5T2Z | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 in complex with darunavir | x-ray diffraction | A, B | 017 | — |
| 6O54 | Crystal Structure of multi-drug resistant HIV-1 protease PR-S17 (D25N) | x-ray diffraction | X | CL | — |
| 6O54 | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 (D25N) | x-ray diffraction | X | CL | — |
| 6O57 | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 with a substrate analog P2-nc in P41 | x-ray diffraction | A, B | — | — |
| 6O5A | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 with a substrate analog P2-nc in P61 | x-ray diffraction | A, B | — | — |
| 6O5X | Crystal structure of multi-drug resistant HIV-1 protease pr-S17 with substrate analog ca-P2 | x-ray diffraction | A, B, C, D | CL, NA | — |
Ligands
Elsewhere
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