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AN ANION BINDING SITE IN HUMAN ALDOSE REDUCTASE: MECHANISTIC IMPLICATIONS FOR THE BINDING OF CITRATE, CACODYLATE, AND GLUCOSE-6-PHOSPHATE[OXIDOREDUCTASE]
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REFINED 1.8 ANGSTROMS STRUCTURE OF HUMAN ALDOSE REDUCTASE COMPLEXED WITH THE POTENT INHIBITOR ZOPOLRESTAT[OXIDOREDUCTASE(NADP)]
CITRATE BOUND, C298A/W219Y MUTANT HUMAN ALDOSE REDUCTASE[OXIDOREDUCTASE]
ALRESTATIN BOUND TO C298A/W219Y MUTANT HUMAN ALDOSE REDUCTASE[OXIDOREDUCTASE]
AN UNLIKELY SUGAR SUBSTRATE SITE IN THE 1.65 ANGSTROMS STRUCTURE OF THE HUMAN ALDOSE REDUCTASE HOLOENZYME IMPLICATED IN DIABETIC COMPLICATIONS[OXIDOREDUCTASE]
THE CRYSTAL STRUCTURE OF THE ALDOSE REDUCTASE NADPH BINARY COMPLEX[OXIDOREDUCTASE]
Human Aldose Reductase in complex with NADP+ and the inhibitor IDD594 at 0.66 Angstrom[OXIDOREDUCTASE]
Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (2)[OXIDOREDUCTASE]
Human Aldose Reductase complexed with novel naphtho[1,2-d]isothiazole acetic acid derivative (3)[OXIDOREDUCTASE]
Human aldose reductase complexed with nitro-substituted IDD-type inhibitor[OXIDOREDUCTASE]
Human aldose reductase complexed with halogenated IDD-type inhibitor[OXIDOREDUCTASE]
Human aldose reductase complexed with nitrofuryl-oxadiazol inhibitor at 1.55 A[OXIDOREDUCTASE]
Human aldose reductase with uracil-type inhibitor at 1.42A[OXIDOREDUCTASE]
Human aldose reductase mutant S302R complexed with IDD 393[OXIDOREDUCTASE]
Human aldose reductase mutant S302R complexed with uracil-type inhibitor[OXIDOREDUCTASE]
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