PDB 5ou0

PDB Information

PDB5OU0
MethodX-RAY DIFFRACTION
Host OrganismEscherichia coli
Gene SourceHomo 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.
Crespo, I., Gimenez-Dejoz, J., Porte, S., Cousido-Siah, A., Mitschler, A., Podjarny, A., Pratsinis, H., Kletsas, D., Pares, X., Ruiz, F.X., Metwally, K., Farres, J.
Eur J Med Chem
HeaderOxidoreductase
Released2017-08-23
Resolution0.940
CATH Insert Date03 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
5ou0A00 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
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