Research workbench
Crystal structure of inla S192N Y369S/HEC1 complex
Analyse Crystal structure of inla S192N Y369S/HEC1 complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2OMV
- Type
- protein
- Length
- 563 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Internalin-a; Epithelial-cadherin
- UniProt
- P25146, P12830
- Ligands
- CA, CL
- Pockets
- 4 · best druggability 0.67
Structure
x-ray diffraction · 2 distinct chains · 14% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Internalin-a | protein | 460 | 16% helix, 23% strand | P25146 |
| B | Epithelial-cadherin | protein | 103 | 4% helix, 45% strand | P12830 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 294 | 0.67 | 0.83 | 40 | empty |
| 2 | 120 | 0.52 | 0.82 | 28 | empty |
| 3 | 139 | 0.52 | 0.80 | 29 | CL |
| 4 | 136 | 0.41 | 0.74 | 27 | empty |
Interfaces
1 interface between chains.
- A–B · 1388 Ų buried · 15 hydrogen bonds · protein-protein
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 P25146
- Every structure of UniProt P12830
- Elsewhere: RCSB PDB 2OMV · PDBe 2OMV · UniProt P25146 · UniProt P12830
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.