Research workbench
Crystal structure of LRP6-E1E2
Analyse Crystal structure of LRP6-E1E2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3S94
- Type
- protein
- Length
- 1,170 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Low-density lipoprotein receptor-related protein 6
- UniProt
- O75581
- Ligands
- NAG
- Pockets
- 13 · best druggability 0.82
Structure
x-ray diffraction · 2 distinct chains · 2% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Low-density lipoprotein receptor-related protein 6 | protein | 587 | 2% helix, 46% strand | O75581 |
| B | Low-density lipoprotein receptor-related protein 6 | protein | 583 | 1% helix, 44% strand | O75581 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 282 | 0.82 | 0.93 | 50 | empty |
| 2 | 304 | 0.80 | 0.91 | 47 | empty |
| 3 | 78 | 0.76 | 0.98 | 18 | empty |
| 4 | 77 | 0.74 | 0.98 | 18 | empty |
| 5 | 465 | 0.62 | 0.76 | 54 | empty |
Interfaces
1 interface between chains.
- A–B · 54 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 12 disulfide, 3 glycan (disulfide, N-glycosylation).
Compared structures
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 O75581
- Elsewhere: RCSB PDB 3S94 · PDBe 3S94 · UniProt O75581
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