Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

5OUK

Crystal structure of human AKR1B1 complexed with NADP+ and compound 41

Summary for 5OUK
Entry DOI10.2210/pdb5ouk/pdb
Related4IGS 5OU0 5OUJ
DescriptorAldose reductase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, 2-[9-fluoranyl-5-(4-methoxyphenyl)-3-methyl-1-oxidanylidene-pyrimido[4,5-c]quinolin-2-yl]ethanoic acid, ... (4 entities in total)
Functional Keywordsalpha-beta tim barrel, cytosol, aldo-keto reductase, pyrimido[4, 5-c]quinolone-2-acetic acid scaffold, oxidoreductase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight37035.11
Authors
Cousido-Siah, A.,Ruiz, F.X.,Mitschler, A.,Metwally, K.,Podjarny, A. (deposition date: 2017-08-24, release date: 2018-05-09, Last modification date: 2024-01-17)
Primary citationCrespo, 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.
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, 152:160-174, 2018
Cited by
PubMed: 29705708
DOI: 10.1016/j.ejmech.2018.04.015
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (0.959 Å)
Structure validation

218853

PDB entries from 2024-04-24

PDB statisticsPDBj update infoContact PDBjnumon