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Crystal analysis of the complex structure, E342A-cellotetraose, of endocellulase from pyrococcus horikoshii

Analyse Crystal analysis of the complex structure, E342A-cellotetraose, of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3QHM
Type
protein
Length
1,131 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
458AA long hypothetical endo-1,4-beta-glucanase
EC
3.2.1.4
UniProt
O58925
Ligands
BGC
Pockets
7 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C458AA long hypothetical endo-1,4-beta-glucanase (EC 3.2.1.4)protein37729% helix, 17% strandO58925

Ligands and binding sites

  • BGC · beta-D-glucopyranose · sugar · 14 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110760.820.83106BGC
24970.700.8064empty
31940.490.7627BGC
4840.480.8219empty
51730.470.7627BGC

Interfaces

3 interfaces between chains.

  • A–C · 789 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 497 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 246 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 3QHM · Crystal analysis of the complex structure, E342A-cellotetraose, of endocellulase from… · the same entry in another collection · chain A against A, TM-score 1.00

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