Research workbench
Structure of an ubiquitin complex
Analyse Structure of an ubiquitin complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4NQK
- Type
- protein
- Length
- 1,187 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Probable ATP-dependent RNA helicase DDX58; Ubiquitin
- EC
- 3.6.4.13
- UniProt
- O95786, P0CG48
- Pockets
- 15 · best druggability 0.90
Structure
x-ray diffraction · 5 distinct chains · 40% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Probable ATP-dependent RNA helicase DDX58 (EC 3.6.4.13) | protein | 188 | 72% helix, 0% strand | O95786 |
| E | Ubiquitin | protein | 72 | 21% helix, 32% strand | P0CG48 |
| F, J | Ubiquitin | protein | 73 | 21% helix, 30% strand | P0CG48 |
| G, I | Ubiquitin | protein | 71 | 17% helix, 32% strand | P0CG48 |
| H | Ubiquitin | protein | 75 | 16% helix, 31% strand | P0CG48 |
Pockets
15 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1058 | 0.90 | 0.92 | 124 | empty |
| 2 | 256 | 0.77 | 0.90 | 32 | empty |
| 3 | 363 | 0.76 | 0.86 | 48 | empty |
| 4 | 93 | 0.74 | 0.96 | 22 | empty |
| 5 | 84 | 0.73 | 0.96 | 18 | empty |
Interfaces
17 interfaces between chains.
- A–B · 1087 Ų buried · 10 hydrogen bonds · protein-protein
- C–D · 1076 Ų buried · 14 hydrogen bonds · protein-protein
- B–C · 1022 Ų buried · 10 hydrogen bonds · protein-protein
- A–D · 941 Ų buried · 8 hydrogen bonds · protein-protein
- C–H · 708 Ų buried · 8 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 O95786
- Every structure of UniProt P0CG48
- Elsewhere: RCSB PDB 4NQK · PDBe 4NQK · UniProt O95786 · UniProt P0CG48
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