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Hydrolytic catalysis and structural stabilization in a designed metalloprotein

Analyse Hydrolytic catalysis and structural stabilization in a designed metalloprotein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3PBJ
Type
protein
Length
172 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Coil ser L9L-pen L23H
Ligands
ACE, ZN, HG, NA, CL, NH2

Structure

x-ray diffraction · 2 distinct chains · 89% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, D, ECoil ser L9L-pen L23Hprotein2990% helix, 0% strand—
B, FCoil ser L9L-pen L23Hprotein2889% helix, 0% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · 5 copies · chains B, C, D, E, F
  • ZN · Zinc ion · metal · 7 copies · chains A, B, C, D, E, F
  • HG · Mercury (II) ion · metal · 2 copies · chains A, B, C, D, E, F
  • NA · Sodium ion · metal · chains B, E
  • CL · Chloride ion · ion · 3 copies · chains A, B, C, E, F
  • NH2 · Amino group · ion · 2 copies · chains D, E

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Interfaces

7 interfaces between chains.

  • A–C · 625 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 618 Ų buried · 4 hydrogen bonds · protein-protein
  • D–F · 593 Ų buried · 5 hydrogen bonds · protein-protein
  • D–E · 591 Ų buried · 2 hydrogen bonds · protein-protein
  • E–F · 586 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified, 5 covalent (nonstandard, covalent ligand).

Compared structures

  • 3PBJ · Hydrolytic catalysis and structural stabilization in a designed metalloprotein · the same entry in another collection · chain A against A, TM-score 1.00

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