Research workbench
Structure of gak kinase in complex with nanobody (NBGAK_4)
Analyse Structure of gak kinase in complex with nanobody (NBGAK_4) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4C59
- Type
- protein
- Length
- 387 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cyclin-G-associated kinase; Nanobody
- EC
- 2.7.11.1
- UniProt
- O14976
- Ligands
- FEF
- Pockets
- 3 · best druggability 0.64
Structure
x-ray diffraction · 2 distinct chains · 27% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cyclin-G-associated kinase (EC 2.7.11.1) | protein | 266 | 36% helix, 21% strand | O14976 |
| B | Nanobody | protein | 121 | 8% helix, 50% strand | — |
Ligands and binding sites
- FEF · (2Z,3E)-2,3'-biindole-2',3(1H,1'H)-dione 3-{O-[(3R)-3,4-dihydroxybutyl]oxime} · ligand · chains A
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 | 490 | 0.64 | 0.77 | 51 | empty |
| 2 | 305 | 0.64 | 0.80 | 37 | FEF |
| 3 | 57 | 0.43 | 0.82 | 14 | empty |
Interfaces
1 interface between chains.
- A–B · 620 Ų buried · 13 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 disulfide (disulfide).
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 O14976
- Elsewhere: RCSB PDB 4C59 · PDBe 4C59 · UniProt O14976
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