PDB 5ouk
PDB Information
| PDB | 5OUK |
| Method | X-RAY DIFFRACTION |
| Host Organism | Escherichia coli |
| Gene Source | Homo sapiens |
| Primary Citation | Design, synthesis, structure-activity relationships and X-ray structural studies of novel 1-oxopyrimido[4,5-c]quinoline-2-acetic acid derivatives as selective and potent inhibitors of human aldose reductase.
Eur J Med Chem
|
| Header | Oxidoreductase |
| Released | 2017-08-24 |
| Resolution | 0.960 |
| CATH Insert Date | 03 Jun, 2018 |
PDB Images (3)
PDB Prints
PDB Chains (1)
| Chain ID | Date inserted into CATH | CATH Status |
|---|---|---|
| A | 03 Jun, 2018 | Chopped |
CATH Domains (1)
| Domain ID | Date inserted into CATH | Superfamily | CATH Status |
|---|---|---|---|
| 5oukA00 | 27 Jun, 2018 | 3.20.20.100 | Assigned |
UniProtKB Entries (1)
| Accession | Gene ID | Taxon | Description |
|---|---|---|---|
| P15121 | ALDR_HUMAN | Homo sapiens | Aldo-keto reductase family 1 member B1 |
