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Glutathione transferase E6 from drosophila melanogaster

Analyse Glutathione transferase E6 from drosophila melanogaster in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4YH2
Type
protein
Length
881 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione S transferase E6
EC
2.5.1.18
UniProt
A1ZB71
Ligands
GSH
Pockets
11 · best druggability 0.87

Structure

x-ray diffraction · 4 distinct chains · 58% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S transferase E6 (EC 2.5.1.18)protein22159% helix, 10% strandA1ZB71
BGlutathione S transferase E6 (EC 2.5.1.18)protein21958% helix, 10% strandA1ZB71
CGlutathione S transferase E6 (EC 2.5.1.18)protein22058% helix, 10% strandA1ZB71
DGlutathione S transferase E6 (EC 2.5.1.18)protein22157% helix, 10% strandA1ZB71

Ligands and binding sites

  • GSH · Glutathione · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110710.870.88105GSH
210810.870.88105GSH
31030.490.8126empty
4910.470.8121empty
51400.430.7520empty

Interfaces

5 interfaces between chains.

  • B–D · 1446 Ų buried · 9 hydrogen bonds · protein-protein
  • A–C · 1437 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 397 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 79 Ų buried · 1 hydrogen bond · protein-protein
  • C–D · 23 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4YH2 · Glutathione Transferase E6 from Drosophila melanogaster · the same entry in another collection · chain A against A, TM-score 1.00

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