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Inactivated mutant (D140A) of Hyperthermophilic GH6 cellobiohydrolase II (HmCel6A) in complex with hexasaccharide

Analyse Inactivated mutant (D140A) of Hyperthermophilic GH6 cellobiohydrolase II… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6K55
Type
protein
Length
1,284 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.883
Source
Ardenticatenia bacterium
Molecule
Glucanase
EC
3.2.1.-
Ligands
BGC, MG
Pockets
11 · best druggability 0.80

Structure

x-ray diffraction · resolution 2.883 · 1 distinct chain · 34% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CGlucanase (EC 3.2.1.-)protein42834% helix, 13% strand—

Ligands and binding sites

  • BGC · beta-D-glucopyranose · sugar · 21 copies · chains A, B, C
  • MG · Magnesium ion · metal · 6 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16900.800.8569BGC
26990.800.8478MG
37010.800.8464BGC
46660.790.8464BGC
54550.700.8152empty

Interfaces

2 interfaces between chains.

  • A–C · 937 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 586 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 3 glycan (disulfide, glycation).

Compared structures

  • 6K55 · Inactivated mutant (D140A) of hyperthermophilic GH6 cellobiohydrolase II (HMCEL6A) in… · the same entry in another collection · chain A against A, TM-score 1.00

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