Research workbench
Azurin mutant M121A
Analyse Azurin mutant M121A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2TSA
- Type
- protein
- Length
- 512 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Azurin
- UniProt
- P00282
- Ligands
- CU
- Pockets
- 4 · best druggability 0.74
Structure
x-ray diffraction · 1 distinct chain · 15% helix, 34% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Azurin | protein | 128 | 15% helix, 34% strand | P00282 |
Ligands and binding sites
- CU · Copper (II) ion · metal · 4 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 348 | 0.74 | 0.86 | 38 | empty |
| 2 | 259 | 0.71 | 0.86 | 27 | empty |
| 3 | 270 | 0.65 | 0.82 | 49 | empty |
| 4 | 205 | 0.62 | 0.83 | 35 | empty |
Interfaces
6 interfaces between chains.
- A–C · 504 Ų buried · 0 hydrogen bonds · protein-protein
- B–D · 484 Ų buried · 0 hydrogen bonds · protein-protein
- A–D · 414 Ų buried · 5 hydrogen bonds · protein-protein
- B–C · 407 Ų buried · 3 hydrogen bonds · protein-protein
- C–D · 357 Ų buried · 1 hydrogen bond · protein-protein
Modifications
Observed in the structure: 4 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 P00282
- Elsewhere: RCSB PDB 2TSA · PDBe 2TSA · UniProt P00282
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