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MolNFT v1 · #169984 · protein

The structure of the M60 catalytic domain from clostridium perfringens zmpc

6XSZ · Zmpc glycopeptidase: “The structure of the M60 catalytic domain from clostridium perfringens zmpc”. X-ray diffraction, 1 ligand (ZN), 15 pockets (best druggability 0.77). MolNFT v1 #169984 on GenesisL1: 3D structure, binding sites…

PDB
6XSZ
Type
protein
Length
2,038 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Zmpc glycopeptidase
UniProt
F8UNJ8
Ligands
ZN
Pockets
15 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AZmpc glycopeptidaseprotein51033% helix, 23% strandF8UNJ8
B, CZmpc glycopeptidaseprotein50933% helix, 23% strandF8UNJ8
DZmpc glycopeptidaseprotein51033% helix, 21% strandF8UNJ8

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · 23 copies · chains A, B, C, D

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

Pockets

15 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111170.770.79108ZN, EDO
211910.760.78106ZN, EDO
36970.630.7365empty
42240.510.7635empty
51260.410.7525empty

Interfaces

4 interfaces between chains.

  • A–D · 836 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 826 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 314 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 133 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6XSZ · The structure of the M60 catalytic domain from Clostridium perfringens ZmpC · the same entry in another collection · chain A against A, TM-score 1.00

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