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Crystal structure of poplar glutathione transferase F1

Analyse Crystal structure of poplar glutathione transferase F1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RI6
Type
protein
Length
428 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phi class glutathione transferase GSTF1
EC
2.5.1.18
UniProt
A9PHH6
Ligands
GSH
Pockets
5 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 59% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPhi class glutathione transferase GSTF1 (EC 2.5.1.18)protein21459% helix, 7% strandA9PHH6

Ligands and binding sites

  • GSH · Glutathione · ligand · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111630.740.7777GSH, MES
2800.600.8927empty
3800.380.7717empty
41080.380.7515empty
5910.310.7216empty

Interfaces

1 interface between chains.

  • A–B · 1454 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 4RI6 · Crystal structure of poplar glutathione transferase F1 · the same entry in another collection · chain A against A, TM-score 1.00

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