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Apo-structure of metalloprotease ZMP1 variant E143A from clostridium difficile

Analyse Apo-structure of metalloprotease ZMP1 variant E143A from clostridium difficile in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5A0S
Type
protein
Length
390 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Zinc metalloprotease ZMP1
EC
3.4.24.-
UniProt
Q183R7
Ligands
ZN
Pockets
2 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 53% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BZinc metalloprotease ZMP1 (EC 3.4.24.-)protein19553% helix, 7% strandQ183R7

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18400.760.8068ZN
22730.600.7930ZN

Interfaces

1 interface between chains.

  • A–B · 444 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 5A0S · Apo-structure of metalloprotease Zmp1 variant E143A from Clostridium difficile · the same entry in another collection · chain A against A, TM-score 1.00
  • Q183R7 · AlphaFold monomer V2.0 prediction for pro-pro endopeptidase (Q183R7) · a predicted model of the same protein · chain A against A, TM-score 0.98

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