UniProt B5MCN7
Nuclear receptor coactivator 1 (B5MCN7)
Nuclear receptor coactivator 1 (UniProt B5MCN7): 12 experimental structures on GenesisL1, 1 ligand bound, 7 pockets. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- B5MCN7
- Protein
- Nuclear receptor coactivator 1
- Experimental structures
- 12
- Predicted models
- 0
- Ligands
- 1
- Pockets
- 7 · 3 records with a druggable one
Structures
12 records of B5MCN7 in the MolNFT archive: 12 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 5E7V | Potent Vitamin D Receptor Agonist | x-ray diffraction | B | — | — |
| 5E7V | Potent vitamin D receptor agonist | x-ray diffraction | B | — | — |
| 6A5W | FXR-LBD with HNC143 and SRC1 | x-ray diffraction | B, D | — | 1 (best 0.79) |
| 6A5W | Fxr-lbd with HNC143 and SRC1 | x-ray diffraction | B, D | — | — |
| 6A5X | FXR-LBD with HNC180 and SRC1 | x-ray diffraction | B | SO4 | 1 (best 0.45) |
| 6A5X | Fxr-lbd with HNC180 and SRC1 | x-ray diffraction | B | SO4 | — |
| 6A5Y | Crystal structure of human FXR/RXR-LBD heterodimer bound to HNC143 and 9cRA and SRC1 | x-ray diffraction | B, F | — | — |
| 6A5Y | Crystal structure of human FXR/RXR-lbd heterodimer bound to HNC143 and 9CRA and SRC1 | x-ray diffraction | B, F | — | — |
| 6A5Z | Crystal structure of human FXR/RXR-LBD heterodimer bound to HNC180 and 9cRA and SRC1 | x-ray diffraction | E, F, G, I | — | 3 (best 0.65) |
| 6A5Z | Crystal structure of human FXR/RXR-lbd heterodimer bound to HNC180 and 9CRA and SRC1 | x-ray diffraction | E, F, G, I | — | — |
| 6A60 | Crystal structure of human FXR/RXR-LBD heterodimer bound to GW4064 and 9cRA and SRC1 | x-ray diffraction | B, F | — | 2 (best 0.71) |
| 6A60 | Crystal structure of human FXR/RXR-lbd heterodimer bound to GW4064 and 9CRA and SRC1 | x-ray diffraction | B, F | — | — |
Ligands
- SO4 · Sulfate ion · in 2 records
Elsewhere
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