Research workbench
Crystal structure of a glutathione-S-transferase from antarctic clam laternula elliptica in a complex with glutathione
Analyse Crystal structure of a glutathione-S-transferase from antarctic clam laternula… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3QAW
- Type
- protein
- Length
- 219 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Rho-class glutathione S-transferase
- EC
- 2.5.1.18
- UniProt
- B9VX79
- Ligands
- GSH
- Pockets
- 1 · best druggability 0.35
Structure
x-ray diffraction · 1 distinct chain · 55% helix, 7% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Rho-class glutathione S-transferase (EC 2.5.1.18) | protein | 219 | 55% helix, 7% strand | B9VX79 |
Ligands and binding sites
- GSH · Glutathione · ligand · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 85 | 0.35 | 0.75 | 23 | empty |
Compared structures
- 3QAW · Crystal structure of a glutathione-S-transferase from Antarctic clam Laternula elliptica… · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt B9VX79
- Elsewhere: RCSB PDB 3QAW · PDBe 3QAW · UniProt B9VX79
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