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Crystal structure of a GH128 (subgroup VI) exo-beta-1,3-glucanase from aureobasidium namibiae (ANGH128_VI)

Analyse Crystal structure of a GH128 (subgroup VI) exo-beta-1,3-glucanase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6UB8
Type
protein
Length
2,487 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GLYCO_HYDRO_CC domain-containing protein
UniProt
A0A074W9U7
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, G, I, JGLYCO_HYDRO_CC domain-containing proteinprotein24940% helix, 18% strandA0A074W9U7
E, F, HGLYCO_HYDRO_CC domain-containing proteinprotein24840% helix, 18% strandA0A074W9U7

Ligands and binding sites

  • GOL · Glycerol · additive · 33 copies · chains A, H, B, C, I, D, E, F, G, J

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

Pockets

20 pockets found on a 1 Å grid, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110550.830.84115GOL
211810.830.84129GOL
38200.830.8587empty
411010.820.83118GOL
51140.680.9127GOL

Interfaces

21 interfaces between chains.

  • E–J · 1181 Ų buried · 15 hydrogen bonds · protein-protein
  • C–D · 1155 Ų buried · 14 hydrogen bonds · protein-protein
  • B–F · 1143 Ų buried · 13 hydrogen bonds · protein-protein
  • A–G · 1140 Ų buried · 18 hydrogen bonds · protein-protein
  • H–I · 1107 Ų buried · 18 hydrogen bonds · protein-protein

Compared structures

  • 6UB8 · Crystal structure of a GH128 (subgroup VI) exo-beta-1,3-glucanase from Aureobasidium… · the same entry in another collection · chain A against A, TM-score 1.00

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