Research workbench
Mamk non-polymerising A278D mutant bound to amppnp
Analyse Mamk non-polymerising A278D mutant bound to amppnp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5LJW
- Type
- protein
- Length
- 656 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Actin-like ATPase
- UniProt
- Q2W8Q6
- Ligands
- ANP, MG
- Pockets
- 7 · best druggability 0.76
Structure
x-ray diffraction · 2 distinct chains · 41% helix, 25% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Actin-like ATPase | protein | 331 | 41% helix, 24% strand | Q2W8Q6 |
| B | Actin-like ATPase | protein | 325 | 40% helix, 26% strand | Q2W8Q6 |
Ligands and binding sites
- ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
- MG · Magnesium ion · metal · 2 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 968 | 0.76 | 0.78 | 92 | MG, ANP |
| 2 | 382 | 0.61 | 0.77 | 49 | MG, ANP |
| 3 | 121 | 0.46 | 0.78 | 18 | empty |
| 4 | 136 | 0.41 | 0.75 | 24 | empty |
| 5 | 75 | 0.36 | 0.76 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 661 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 Q2W8Q6
- Elsewhere: RCSB PDB 5LJW · PDBe 5LJW · UniProt Q2W8Q6
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