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X-ray crystal structure of chitosan-binding module 1 derived from CHITOSANASE/GLUCANASE from paenibacillus sp. ik-5.

Analyse X-ray crystal structure of chitosan-binding module 1 derived from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4ZXE
Type
protein
Length
400 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GLUCANASE/CHITOSANASE
EC
3.2.1.4, 3.2.1.132
UniProt
Q93IE7
Ligands
SO4
Pockets
5 · best druggability 0.56

Structure

x-ray diffraction · 2 distinct chains · 3% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BGLUCANASE/CHITOSANASE (EC 3.2.1.4, 3.2.1.132)protein1324% helix, 52% strandQ93IE7
CGLUCANASE/CHITOSANASE (EC 3.2.1.4, 3.2.1.132)protein1363% helix, 51% strandQ93IE7

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C
  • EDO · 1,2-ethanediol · additive · 18 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11440.560.8225empty
2980.400.7722EDO
3900.390.7722EDO
4780.360.7621EDO
5570.340.7814empty

Interfaces

3 interfaces between chains.

  • B–C · 564 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 507 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 493 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4ZXE · X-ray crystal structure of chitosan-binding module 1 derived from chitosanase/glucanase… · the same entry in another collection · chain A against A, TM-score 1.00

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