Research workbench
Crystal structure of leishmania infantum trypanothione reductase in complex with NADPH and trypanothione
Analyse Crystal structure of leishmania infantum trypanothione reductase in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4ADW
- Type
- protein
- Length
- 976 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Trypanothione reductase
- EC
- 1.8.1.12
- UniProt
- A4HSF7
- Ligands
- FAD, NDP, GCG
- Pockets
- 6 · best druggability 0.86
Structure
x-ray diffraction · 1 distinct chain · 31% helix, 26% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Trypanothione reductase (EC 1.8.1.12) | protein | 488 | 31% helix, 26% strand | A4HSF7 |
Ligands and binding sites
- FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
- GCG · Bis(gamma-glutamyl-cysteinyl-glycinyl)spermidine · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1097 | 0.86 | 0.86 | 109 | empty |
| 2 | 836 | 0.82 | 0.84 | 102 | FAD, NDP |
| 3 | 774 | 0.82 | 0.85 | 90 | FAD, NDP |
| 4 | 91 | 0.44 | 0.79 | 16 | empty |
| 5 | 98 | 0.35 | 0.74 | 14 | empty |
Interfaces
1 interface between chains.
- A–B · 3354 Ų buried · 34 hydrogen bonds · protein-protein
Compared structures
- 4ADW · Crystal structure of leishmania infantum trypanothione reductase in complex with NADPH… · 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 A4HSF7
- Elsewhere: RCSB PDB 4ADW · PDBe 4ADW · UniProt A4HSF7
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