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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).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAzurinprotein12815% helix, 34% strandP00282

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.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13480.740.8638empty
22590.710.8627empty
32700.650.8249empty
42050.620.8335empty

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

  • 2TSA · Azurin mutant M121A · the same entry in another collection · chain B against B, TM-score 1.00
  • P00282 · AlphaFold monomer V2.0 prediction for azurin (P00282) · a predicted model of the same protein · chain C against A, TM-score 0.99

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