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Zinc-bound glycoside hydrolase 61 E from thielavia terrestris

Analyse Zinc-bound glycoside hydrolase 61 E from thielavia terrestris in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3EII
Type
protein
Length
832 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein GH61E
Ligands
NAG, ZN, SO4
Pockets
5 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 2% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DProtein GH61Eprotein2082% helix, 32% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B, C, D
  • ZN · Zinc ion · metal · 6 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 11 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 2 copies · chains A, C, D

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18740.770.80100ZN, GOL
24230.600.7656empty
32780.510.7538ZN
4660.400.8026empty
5720.390.7818empty

Interfaces

5 interfaces between chains.

  • B–D · 397 Ų buried · 2 hydrogen bonds · protein-protein
  • A–C · 368 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 358 Ų buried · 1 hydrogen bond · protein-protein
  • C–D · 176 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 82 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 3EII · Zinc-bound glycoside hydrolase 61 E from Thielavia terrestris · the same entry in another collection · chain A against A, TM-score 1.00

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