PDB 5ou0

PDB Links
Overview

PDB Information

PDB	5OU0
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. 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
Header	Oxidoreductase
Released	2017-08-23
Resolution	0.940
CATH Insert Date	03 Jun, 2018

PDB Images (3)

Image of CATH 5ou0

5ou0

PDB 5ou0

Image of CATH 5ou0A

5ou0A

PDB Chain 5ou0A

Image of CATH 5ou0A00

5ou0A00

CATH Domain 5ou0A00

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