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Crystal structure of a GH131 beta-glucanase catalytic domain from podospora anserina

Analyse Crystal structure of a GH131 beta-glucanase catalytic domain from podospora… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4LE3
Type
protein
Length
983 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-glucanase
UniProt
J7K096
Pockets
8 · best druggability 0.70

Structure

x-ray diffraction · 4 distinct chains · 5% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-glucanaseprotein2496% helix, 43% strandJ7K096
BBeta-glucanaseprotein2455% helix, 43% strandJ7K096
CBeta-glucanaseprotein2425% helix, 44% strandJ7K096
DBeta-glucanaseprotein2475% helix, 43% strandJ7K096

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13130.700.8434empty
21640.560.8132empty
33390.560.7533empty
41010.500.8224empty
51240.450.7823empty

Interfaces

3 interfaces between chains.

  • A–B · 742 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 332 Ų buried · 2 hydrogen bonds · protein-protein
  • A–C · 112 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 4LE3 · Crystal structure of a GH131 beta-glucanase catalytic domain from Podospora anserina · the same entry in another collection · chain A against A, TM-score 1.00

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