Research workbench
Crystal structure of the er-alpha ligand-binding domain (Y537S) in complex with the obhs-asc analog, (E)-6-(4-((1R,4S,6R)-6-((4- BROMOPHENOXY)SULFONYL)-3-(4-hydroxyphenyl)-7-OXABICYCLO[2.2.1]HEPT-2- en-2-YL)PHENYL)HEX-5-enoic acid
Analyse Crystal structure of the er-alpha ligand-binding domain (Y537S) in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5TMM
- Type
- protein
- Length
- 462 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Estrogen receptor; Nuclear receptor coactivator 2
- UniProt
- P03372, Q15596
- Ligands
- 7M4
- Pockets
- 7 · best druggability 0.79
Structure
x-ray diffraction · 4 distinct chains · 69% helix, 3% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Estrogen receptor | protein | 223 | 69% helix, 3% strand | P03372 |
| B | Estrogen receptor | protein | 222 | 68% helix, 4% strand | P03372 |
| C | Nuclear receptor coactivator 2 | protein | 8 | 75% helix, 0% strand | Q15596 |
| D | Nuclear receptor coactivator 2 | protein | 9 | 56% helix, 0% strand | Q15596 |
Ligands and binding sites
- 7M4 · 6-{4-[(1S,4S,6S)-6-[(4-bromophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenyl}hex-5-enoic acid · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 312 | 0.79 | 0.90 | 31 | 7M4 |
| 2 | 283 | 0.79 | 0.90 | 30 | 7M4 |
| 3 | 76 | 0.65 | 0.91 | 17 | empty |
| 4 | 77 | 0.64 | 0.91 | 17 | empty |
| 5 | 123 | 0.46 | 0.78 | 21 | empty |
Interfaces
3 interfaces between chains.
- A–B · 1727 Ų buried · 30 hydrogen bonds · protein-protein
- B–D · 498 Ų buried · 2 hydrogen bonds · protein-protein
- A–C · 440 Ų buried · 3 hydrogen bonds · protein-protein
Compared structures
- 5TMM · Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the… · the same entry in another collection · chain A against A, TM-score 1.00
- P03372 · AlphaFold monomer V2.0 prediction for estrogen receptor (P03372) · a predicted model of the same protein · chain A against A, TM-score 0.99
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P03372
- Every structure of UniProt Q15596
- Elsewhere: RCSB PDB 5TMM · PDBe 5TMM · UniProt P03372 · UniProt Q15596
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.