Research workbench
Crystal structure of GRE2 in complex with NADPH complex from candida albicans
Analyse Crystal structure of GRE2 in complex with NADPH complex from candida albicans in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6KWT
- Type
- protein
- Length
- 338 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Methylglyoxal reductase (NADPH-dependent)
- UniProt
- Q5ABT9
- Ligands
- NDP
- Pockets
- 1 · best druggability 0.77
Structure
x-ray diffraction · 1 distinct chain · 43% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Methylglyoxal reductase (NADPH-dependent) | protein | 338 | 43% helix, 16% strand | Q5ABT9 |
Ligands and binding sites
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · 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, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 809 | 0.77 | 0.81 | 75 | NDP |
Modifications
Observed in the structure: 1 covalent (covalent ligand).
Compared structures
- 6KWT · Crystal structure of Gre2 in complex with NADPH complex from Candida albicans · 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 Q5ABT9
- Elsewhere: RCSB PDB 6KWT · PDBe 6KWT · UniProt Q5ABT9
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