Research workbench
Structure of the card-card disk
Analyse Structure of the card-card disk in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5WVC
- Type
- protein
- Length
- 593 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Apoptotic protease-activating factor 1; Caspase
- UniProt
- O14727, A8K7U6
- Ligands
- IOD
- Pockets
- 3 · best druggability 0.81
Structure
x-ray diffraction · 3 distinct chains · 73% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| C, A | Apoptotic protease-activating factor 1 | protein | 95 | 73% helix, 0% strand | O14727 |
| D, B, F | Caspase | protein | 103 | 71% helix, 0% strand | A8K7U6 |
| E | Apoptotic protease-activating factor 1 | protein | 94 | 74% helix, 0% strand | O14727 |
Ligands and binding sites
- IOD · Iodide ion · ion · 11 copies · chains C, D, B, E, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1117 | 0.81 | 0.82 | 78 | IOD |
| 2 | 249 | 0.60 | 0.80 | 20 | empty |
| 3 | 53 | 0.46 | 0.86 | 18 | empty |
Interfaces
10 interfaces between chains.
- D–E · 626 Ų buried · 12 hydrogen bonds · protein-protein
- C–B · 618 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 486 Ų buried · 10 hydrogen bonds · protein-protein
- E–F · 478 Ų buried · 13 hydrogen bonds · protein-protein
- C–D · 468 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 modified (oxidation).
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 O14727
- Every structure of UniProt A8K7U6
- Elsewhere: RCSB PDB 5WVC · PDBe 5WVC · UniProt O14727 · UniProt A8K7U6
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