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1Z3N

Human aldose reductase in complex with NADP+ and the inhibitor lidorestat at 1.04 angstrom

Summary for 1Z3N
Entry DOI10.2210/pdb1z3n/pdb
Related1US0
Descriptoraldose reductase, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, {3-[(4,5,7-TRIFLUORO-1,3-BENZOTHIAZOL-2-YL)METHYL]-1H-INDOL-1-YL}ACETIC ACID, ... (4 entities in total)
Functional Keywordsoxidoreductase, nadp+, lidorestat
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight37302.39
Authors
Van Zandt, M.C.,Jones, M.L.,Gunn, D.E.,Geraci, L.S.,Jones, J.H.,Sawicki, D.R.,Sredy, J.,Jacot, J.L.,Dicioccio, A.T.,Petrova, T.,Mitschler, A.,Podjarny, A.D. (deposition date: 2005-03-14, release date: 2006-03-14, Last modification date: 2024-03-13)
Primary citationVan Zandt, M.C.,Jones, M.L.,Gunn, D.E.,Geraci, L.S.,Jones, J.H.,Sawicki, D.R.,Sredy, J.,Jacot, J.L.,Dicioccio, A.T.,Petrova, T.,Mitschler, A.,Podjarny, A.D.
Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications
J.Med.Chem., 48:3141-3152, 2005
Cited by
PubMed: 15857120
DOI: 10.1021/jm0492094
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.04 Å)
Structure validation

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