Research workbench
Crystal structure of human karyopherin-BETA2 bound to the histone H3 tail
Analyse Crystal structure of human karyopherin-BETA2 bound to the histone H3 tail in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5J3V
- Type
- protein
- Length
- 1,682 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Transportin-1,TRANSPORTIN-1; Histone H3
- UniProt
- Q92973
- Pockets
- 15 · best druggability 0.66
Structure
x-ray diffraction · 3 distinct chains · 70% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Transportin-1,TRANSPORTIN-1 | protein | 835 | 73% helix, 0% strand | Q92973 |
| C, D | Histone H3 | protein | 17 | 35% helix, 0% strand | — |
| B | Transportin-1,TRANSPORTIN-1 | protein | 813 | 67% helix, 0% strand | Q92973 |
Pockets
15 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 61 | 0.66 | 0.94 | 16 | empty |
| 2 | 577 | 0.66 | 0.77 | 45 | empty |
| 3 | 262 | 0.64 | 0.82 | 28 | empty |
| 4 | 489 | 0.63 | 0.76 | 40 | empty |
| 5 | 264 | 0.63 | 0.81 | 39 | empty |
Interfaces
3 interfaces between chains.
- B–D · 977 Ų buried · 22 hydrogen bonds · protein-protein
- A–C · 939 Ų buried · 20 hydrogen bonds · protein-protein
- A–B · 634 Ų buried · 5 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 Q92973
- Elsewhere: RCSB PDB 5J3V · PDBe 5J3V · UniProt Q92973
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