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Nek2 bound to arylaminopurine 6
Analyse Nek2 bound to arylaminopurine 6 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5M57
- Type
- protein
- Length
- 261 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.3
- Source
- Homo sapiens
- Molecule
- Serine/threonine-protein kinase Nek2
- EC
- 2.7.11.1
- UniProt
- P51955
- Ligands
- 4SP
- Pockets
- 3 · best druggability 0.64
Structure
x-ray diffraction · resolution 2.3 · 1 distinct chain · 38% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Serine/threonine-protein kinase Nek2 (EC 2.7.11.1) | protein | 261 | 38% helix, 18% strand | P51955 |
Ligands and binding sites
- 4SP · O6-cyclohexylmethoxy-2-(4'-sulphamoylanilino) purine · 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, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 305 | 0.64 | 0.80 | 35 | empty |
| 2 | 118 | 0.48 | 0.79 | 23 | 4SP |
| 3 | 84 | 0.33 | 0.74 | 16 | empty |
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 P51955
- Elsewhere: RCSB PDB 5M57 · PDBe 5M57 · UniProt P51955
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