Research workbench
Apo KIF14[391-772] in complex with a microtubule
Analyse Apo KIF14[391-772] in complex with a microtubule in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6WWE
- Type
- protein
- Length
- 1,231 residues
- Chains
- 3
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Tubulin alpha-1B chain; Tubulin beta-2B chain; Kinesin-like protein KIF14
- UniProt
- Q2XVP4, A0A287AGU7, L0N7N1
- Ligands
- GTP, GDP, TA1, MG
- Pockets
- 20 · best druggability 0.82
Structure
electron microscopy · 3 distinct chains · 38% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Tubulin alpha-1B chain | protein | 441 | 41% helix, 13% strand | Q2XVP4 |
| B | Tubulin beta-2B chain | protein | 431 | 43% helix, 13% strand | A0A287AGU7 |
| K | Kinesin-like protein KIF14 | protein | 359 | 30% helix, 20% strand | L0N7N1 |
Ligands and binding sites
- GTP · Guanosine-5'-triphosphate · ligand · chains A, B
- GDP · Guanosine-5'-diphosphate · ligand · chains B
- TA1 · Taxol · ligand · chains B
- MG · Magnesium ion · metal · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 269 | 0.82 | 0.94 | 49 | GTP, MG |
| 2 | 989 | 0.79 | 0.81 | 73 | empty |
| 3 | 609 | 0.75 | 0.82 | 68 | empty |
| 4 | 55 | 0.70 | 0.97 | 24 | empty |
| 5 | 107 | 0.67 | 0.90 | 31 | empty |
Interfaces
3 interfaces between chains.
- A–B · 2043 Ų buried · 20 hydrogen bonds · protein-protein
- A–K · 875 Ų buried · 11 hydrogen bonds · protein-protein
- B–K · 713 Ų buried · 10 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 Q2XVP4
- Every structure of UniProt A0A287AGU7
- Every structure of UniProt L0N7N1
- Elsewhere: RCSB PDB 6WWE · PDBe 6WWE · UniProt Q2XVP4 · UniProt A0A287AGU7 · UniProt L0N7N1
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