EC 1.1.1.21 - alditol:NAD(P) + 1- oxidoreductase (aldehyde reductase)
3D structures of EC 1.1.1.21 - aldehyde reductase in Protein Data Bank
updated: 6 January 2022, 2:15
In total: 173 PDB structures of EC 1.1.1.21 - aldehyde reductase:
- 1abn: The Crystal Structure of The Aldose Reductase Nadph Binary Complex
- 1ads: An Unlikely Sugar Substrate Site in The 1.65 Angstroms Structure of The Human Aldose Reductase Holoenzyme Implicated in Diabetic Complications
- 1ah0: Pig Aldose Reductase Complexed with Sorbinil
- 1ah3: Aldose Reductase Complexed with Tolrestat Inhibitor
- 1ah4: Pig Aldose Reductase, Holo Form
- 1az1: Alrestatin Bound to C298A/W219Y Mutant Human Aldose Reductase
- 1az2: Citrate Bound, C298A/W219Y Mutant Human Aldose Reductase
- 1dla: Novel Nadph-binding Domain Revealed by The Crystal Structure of Aldose Reductase
- 1ef3: Fidarestat Bound to Human Aldose Reductase
- 1eko: Pig Aldose Reductase Complexed with Idd384 Inhibitor
- 1el3: Human Aldose Reductase Complexed with Idd384 Inhibitor
- 1iei: Crystal Structure of Human Aldose Reductase Complexed with The Inhibitor Zenarestat.
- 1jez: The Structure of Xylose Reductase, a Dimeric Aldo-keto Reductase from Candida Tenuis
- 1k8c: Crystal Structure of Dimeric Xylose Reductase in Complex with Nadp(h)
- 1mar: Refined 1.8 Angstroms Structure of Human Aldose Reductase Complexed with The Potent Inhibitor Zopolrestat
- 1mi3: 1.8 Angstrom Structure of Xylose Reductase from Candida Tenuis in Complex with Nadh
- 3krb: Structure of Aldose Reductase from Giardia Lamblia at 1.75a Resolution
- 1pwl: Crystal Structure of Human Aldose Reductase Complexed with Nadp and Minalrestat
- 1pwm: Crystal Structure of Human Aldose Reductase Complexed with Nadp and Fidarestat
- 1r38: Crystal Structure of H114A Mutant of Candida Tenuis Xylose Reductase
- 3ghu: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594. Investigation of Global Effects of Radiation Damage on Protein Structure. Forth Stage of Radiation Damage.
- 3ght: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594. Investigation of Global Effects of Radiation Damage on Protein Structure. Third Stage of Radiation Damage.
- 3ghs: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594. Investigation of Global Effects of Radiation Damage on Protein Structure. Second Stage of Radiation Damage.
- 3ghr: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594. Investigation of Global Effects of Radiation Damage on Protein Structure. First Stage of Radiation Damage
- 3g5e: Human Aldose Reductase Complexed with Idd 740 Inhibitor
- 1sm9: Crystal Structure of an Engineered K274RN276D Double Mutant of Xylose Reductase from Candida Tenuis Optimized to Utilize Nad
- 1t40: Crystal Structure of Human Aldose Reductase Complexed with Nadp and Idd552 at Ph 5
- 1t41: Crystal Structure of Human Aldose Reductase Complexed with Nadp and Idd552
- 3dn5: Aldose Reductase in Complex with Novel Biarylic Inhibitor
- 1us0: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594 at 0.66 Angstrom
- 3bcj: Crystal Structure of Aldose Reductase Complexed with 2S4R (stereoisomer of Fidarestat, 2S4S) at 0.78 a
- 1x96: Crystal Structure of Aldose Reductase with Citrates Bound in The Active Site
- 1x97: Crystal Structure of Aldose Reductase Complexed with 2R4S (stereoisomer of Fidarestat, 2S4S)
- 1x98: Crystal Structure of Aldose Reductase Complexed with 2S4R (stereoisomer of Fidarestat, 2S4S)
- 1xgd: Apo R268A Human Aldose Reductase
- 1z3n: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Lidorestat at 1.04 Angstrom
- 1z89: Human Aldose Reductase Complexed with Novel Sulfonyl- Pyridazinone Inhibitor
- 1z8a: Human Aldose Reductase Complexed with Novel Sulfonyl- Pyridazinone Inhibitor
- 2vdg: Barley Aldose Reductase 1 Complex with Butanol
- 2acq: An Anion Binding Site in Human Aldose Reductase: Mechanistic Implications for The Binding of Citrate, Cacodylate, and Glucose-6-phosphate
- 2acr: An Anion Binding Site in Human Aldose Reductase: Mechanistic Implications for The Binding of Citrate, Cacodylate, and Glucose-6-phosphate
- 2acs: An Anion Binding Site in Human Aldose Reductase: Mechanistic Implications for The Binding of Citrate, Cacodylate, and Glucose-6-phosphate
- 2acu: Tyrosine-48 Is The Proton Donor and Histidine-110 Directs Substrate Stereochemical Selectivity in The Reduction Reaction of Human Aldose Reductase: Enzyme Kinetics and The Crystal Structure of The Y48H Mutant Enzyme
- 2agt: Aldose Reductase Mutant Leu 300 pro Complexed with Fidarestat
- 2bgq: Apo Aldose Reductase from Barley
- 2bgs: Holo Aldose Reductase from Barley
- 2r24: Human Aldose Reductase Structure
- 2qxw: Perdeuterated Alr2 in Complex with Idd594
- 2pzn: The Crystallographic Structure of Aldose Reductase Idd393 Complex Confirms Leu300 as a Specificity Determinant
- 2pfh: Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and Idd594. Concentration of Fidarestat in Soaking Solution Is less than Concentration of Idd594.
- 2pf8: Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and Idd594. Concentration of Fidarestat in Soaking Solution Is Equal to Concentration of Idd594.
- 2pev: Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and Idd594. Concentration of Fidarestat in Soaking Solution Exceeds Concentration of Idd594.
- 2pdy: Human Aldose Reductase Double Mutant S302R-C303D Complexed with Fidarestat.
- 2pdx: Human Aldose Reductase Double Mutant S302R-C303D Complexed with Zopolrestat.
- 2pdw: Human Aldose Reductase Mutant C303D Complexed with Fidarestat.
- 2pdu: Human Aldose Reductase Mutant C303D Complexed with Idd393.
- 2pdq: Human Aldose Reductase Mutant C303D Complexed with Uracil- Type Inhibitor.
- 2pdp: Human Aldose Reductase Mutant S302R Complexed with Idd 393.
- 2pdn: Human Aldose Reductase Mutant S302R Complexed with Uracil- Type Inhibitor.
- 2pdm: Human Aldose Reductase Mutant S302R Complexed with Zopolrestat.
- 2pdl: Human Aldose Reductase Mutant L301M Complexed with Tolrestat.
- 2pdk: Human Aldose Reductase Mutant L301M Complexed with Sorbinil.
- 2pdj: Human Aldose Reductase Mutant L300A Complexed with Idd393.
- 2pdi: Human Aldose Reductase Mutant L300A Complexed with Zopolrestat at 1.55 A.
- 2pdh: Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.
- 2pdg: Human Aldose Reductase with Uracil-type Inhibitor at 1.42a.
- 2pdf: Human Aldose Reductase Mutant L300P Complexed with Zopolrestat.
- 2pdc: Human Aldose Reductase Mutant F121P Complexed with Idd393.
- 2pdb: Human Aldose Reductase Mutant F121P Complexed with Zopolrestat.
- 2pd9: Human Aldose Reductase Mutant V47I Complexed with Fidarestat.
- 2pd5: Human Aldose Reductase Mutant V47I Complexed with Zopolrestat
- 2dux: Crystal Structure of Human Aldose Reductase Complexed with Zopolrestat after 3 Days Soaking (3days_soaked_1)
- 2duz: Human Aldose Reductase Complexed with Inhibitor Zopolrestat after 3 Days Soaking (3days_soaked_2)
- 2dv0: Human Aldose Reductase Complexed with Zopolrestat after 6 Days Soaking(6days_soaked_2)
- 2nvd: Human Aldose Reductase Complexed with Novel Naphtho[1,2- D]isothiazole Acetic Acid Derivative (2)
- 2nvc: Human Aldose Reductase Complexed with Novel Naphtho[1,2- D]isothiazole Acetic Acid Derivative (3)
- 2f2k: Aldose Reductase Tertiary Complex with Nadph and Deg
- 2fz8: Human Aldose Reductase Complexed with Inhibitor Zopolrestat at 1.48 A(1 Day Soaking).
- 2fz9: Human Aldose Reductase Complexed with Inhibitor Zopolrestat after Six Days Soaking.
- 2fzb: Human Aldose Reductase Complexed with Four Tolrestat Molecules at 1.5 a Resolution.
- 2fzd: Human Aldose Reductase Complexed with Tolrestat at 1.08 a Resolution.
- 5zcm: Crystal Structure of Xylose Reductase from Debaryomyces Nepalensis in Complex with Nadp-dtt Adduct
- 5zci: Crystal Structure of Apo Form of Xylose Reductase from Debaryomyces Nepalensis
- 2hv5: Human Aldose Reductase Complexed with Inhibitor Zopolrestat after Three Days Soaking (3days_soaked_3)
- 2hvn: Human Aldose Reductase-zopolrestat Complex Obtained by Cocrystallisation after One Day (1day_cocryst)
- 2hvo: Human Aldose Reductase-zopolrestat Complex Obtained by Cocrystallisation (10days_cocryst)
- 2i16: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594 at Temperature of 15k
- 2i17: Human Aldose Reductase in Complex with Nadp+ and The Inhibitor Idd594 at Temperature of 60k
- 2ikg: Aldose Reductase Complexed with Nitrophenyl-oxadiazol Type Inhibitor at 1.43 a
- 2ikh: Human Aldose Reductase Complexed with Nitrofuryl-oxadiazol Inhibitor at 1.55 a
- 2iki: Human Aldose Reductase Complexed with Halogenated Idd-type Inhibitor
- 2ikj: Human Aldose Reductase Complexed with Nitro-substituted Idd- Type Inhibitor
- 2ine: Crystal Structure of Aldose Reductase Complexed with Phenylacetic Acid
- 2inz: Crystal Structure of Aldose Reductase Complexed with 2- Hydroxyphenylacetic Acid
- 2ipw: Crystal Structure of C298A W219Y Aldose Reductase Complexed with Dichlorophenylacetic Acid
- 2iq0: Crystal Structure of Aldose Reductase Complexed with Hexanoic Acid
- 2iqd: Crystal Structure of Aldose Reductase Complexed with Lipoic Acid
- 2is7: Crystal Structure of Aldose Reductase Complexed with Dichlorophenylacetic Acid
- 2isf: Crystal Structure of C298A W219Y Aldose Reductase Complexed with Phenylacetic Acid
- 2j8t: Human Aldose Reductase in Complex with Nadp and Citrate at 0.82 Angstrom
- 6td8: Human Aldose Reductase Mutant L301A in Complex with a Ligand with an Idd Structure ({5-fluoro-2-[(3-nitrobenzyl)carbamoyl]phenoxy}acetic Acid)
- 6t7q: Human Aldose Reductase Mutant L301A in Complex with a Ligand with an Idd Structure (3-({[2-(carboxymethoxy)-4-fluorobenzoyl]amino}methyl) Benzoic Acid)
- 6t5g: Structure of Human Aldose Reductase Mutant L300A with a Citrate Molecule Bound in The Anion Binding Pocket
- 6t3p: Human Aldose Reductase Mutant L300A in Complex with a Ligand with an Idd Structure ({5-fluoro-2-[(3-nitrobenzyl)carbamoyl]phenoxy}acetic Acid)
- 6t27: Structure of Human Aldose Reductase Mutant L301A with a Citrate Molecule Bound in The Anion Binding Pocket
- 6syw: Human Aldose Reductase in Complex with Sar25
- 3lbo: Human Aldose Reductase Mutant T113C Complexed with Idd594
- 3ld5: Human Aldose Reductase Mutant T113S Complexed with Idd594
- 3len: Human Aldose Reductase Mutant T113S Complexed with Zopolrestat
- 3lep: Human Aldose Reductase Mutant T113C in Complex with Idd388
- 3lqg: Human Aldose Reductase Mutant T113A Complexed with Idd388
- 3lql: Human Aldose Reductase Mutant T113A Complexed with Idd 594
- 3lz3: Human Aldose Reductase Mutant T113S Complexed with Idd388
- 3lz5: Human Aldose Reductase Mutant T113V Complexed with Idd594
- 3m4h: Human Aldose Reductase Mutant T113V Complexed with Idd388
- 3q65: Human Aldose Reductase in Complex with Nadp+ in Space Group P212121
- 3q67: Human Aldose Reductase C298S Mutant in Complex with Nadp+ in Space Group P212121
- 3m0i: Human Aldose Reductase Mutant T113V in Complex with Zopolrestat
- 3m64: Human Aldose Reductase Mutant T113V Complexed with Idd393
- 3mb9: Human Aldose Reductase Mutant T113A Complexed with Zopolrestat
- 3mc5: Human Aldose Reductase Mutant T113V in Complex with Idd393 Crystallized in Spacegroup P1
- 3onb: Bond Breakage and Relocation of a Covalently Bound Bromine of Idd594 in a Complex with Har T113A Mutant after Extensive Radiation Dose
- 3onc: Bond Breakage and Relocation of a Covalently Bound Bromine of Idd594 in a Complex with Har T113A Mutant after Moderate Radiation Dose
- 3p2v: Novel Benzothiazepine Inhibitor in Complex with Human Aldose Reductase
- 3t42: Human Aldose Reductase in Complex with a Nitrile-containing Idd Inhibitor
- 3u2c: Aldose Reductase in Complex with Nsaid-type Inhibitor at 1.0 a Resolution
- 3rx2: Crystal Structure of Human Aldose Reductase Complexed with Sulindac Sulfone
- 3rx3: Crystal Structure of Human Aldose Reductase Complexed with Sulindac
- 3rx4: Crystal Structure of Human Aldose Reductase Complexed with Sulindac Sulfide
- 3s3g: Crystal Structure of Human Aldose Reductase Complexed with Tolmetin
- 3v35: Aldose Reductase Complexed with a Nitro Compound
- 3v36: Aldose Reductase Complexed with Glceraldehyde
- 4hbk: Structure of The Aldose Reductase from Schistosoma Japonicum
- 6f8o: AKR1B1 at 3.45 Mgy Radiation Dose.
- 6f84: AKR1B1 at 2.55 Mgy Radiation Dose.
- 6f82: AKR1B1 at 1.65 Mgy Radiation Dose.
- 6f81: AKR1B1 at 0.75 Mgy Radiation Dose.
- 6f7r: AKR1B1 at 0.03 Mgy Radiation Dose.
- 4gca: Complex of Aldose Reductase with Inhibitor Idd 1219
- 4igs: Crystal Structure of Human Aldose Reductase Complexed with Nadp+ and Jf0064
- 4jir: Crystal Structure of Aldose Reductase (AKR1B1) Complexed with Nadp+ and Epalrestat
- 4lau: Crystal Structure of Human Ar Complexed with Nadp+ and {2-[(4- Bromobenzyl)carbamoyl]-5-chlorophenoxy}acetic Acid
- 4laz: Crystal Structure of Human Ar Complexed with Nadp+ and {5-chloro-2- [(4-iodobenzyl)carbamoyl]phenoxy}acetic Acid
- 4lb3: Crystal Structure of Human Ar Complexed with Nadp+ and {5-chloro-2- [(2-fluoro-4-iodobenzyl)carbamoyl]phenoxy}acetic Acid
- 4lb4: Crystal Structure of Human Ar Complexed with Nadp+ and {2-[(4-bromo-2, 3,5,6-tetrafluorobenzyl)carbamoyl]-5-chlorophenoxy}acetic Acid
- 4lbr: Crystal Structure of Human Ar Complexed with Nadp+ and {5-chloro-2- [(2,6-difluoro-4-iodobenzyl)carbamoyl]phenoxy}acetic Acid
- 4lbs: Crystal Structure of Human Ar Complexed with Nadp+ and {2-[(4-bromo-2, 6-difluorobenzyl)carbamoyl]-5-chlorophenoxy}acetic Acid
- 5ouk: Crystal Structure of Human AKR1B1 Complexed with Nadp+ and Compound 41
- 5ouj: Crystal Structure of Human AKR1B1 Complexed with Nadp+ and Compound 39
- 5ou0: Crystal Structure of Human AKR1B1 Complexed with Nadp+ and Compound 37
- 5ha7: Human Aldose Reductase in Complex with Nadp+ and Wy14643 in Space Group P212121
- 4nkc: Human Aldose Reductase Complexed with Schl7764 at 1.12 a
- 4qx4: Human Aldose Reductase Complexed with a Ligand with a New Scaffold at 1.26 a
- 4pr4: Human Aldose Reductase Complexed with Schl7802 at 1.06 a
- 4prr: Human Aldose Reductase Complexed with Schl7815 ((3-[3-(5-nitrofuran-2- Yl)phenyl]propanoic Acid)at 1.01 a
- 4prt: Human Aldose Reductase Complexed with Schl12221 ({2-[5-(3- Nitrophenyl)furan-2-yl]phenyl}acetic Acid) at 0.96 a
- 4puu: Human Aldose Reductase Complexed with a Ligand with an Idd Structure (2-(2-carbamoyl-5-fluoro-phenoxy)acetic Acid) at 1.14 a
- 4puw: Human Aldose Reductase Complexed with a Ligand with an Idd Structure (2-[5-fluoro-2-(prop-2-ynylcarbamoyl)phenoxy]acetic Acid) at 1.12 a
- 4yu1: Human Aldose Reductase Complexed with Schl12134 (3-[5-(3-nitrophenyl)- 2-thienyl]propanoic Acid) at 1.02 a
- 4ys1: Human Aldose Reductase Complexed with a Ligand with an Idd Structure (2) at 1.07 A.
- 4q7b: Human Aldose Reductase Complexed with a Ligand with an Idd Structure ([2-(benzylcarbamoyl)-5-fluorophenoxy]acetic Acid) at 1.19 a
- 4qbx: Human Aldose Reductase Complexed with a Ligand with an Idd Structure ({5-fluoro-2-[(3-nitrobenzyl)carbamoyl]phenoxy}acetic Acid) at 0.98 a
- 4qr6: Human Aldose Reductase Complexed with a Ligand with an Idd Structure (2-[2-(1,3-benzothiazol-2-ylmethylcarbamoyl)-5-fluoro-phenoxy]acetic Acid) at 1.05 a
- 4qxi: Crystal Structure of Human Ar Complexed with Nadp+ and Ak198
- 4rpq: Human Aldose Reductase Complexed with a Ligand with an Idd Structure at 1.20 a (1)
- 4xzh: Crystal Structure of Human Aldose Reductase Complexed with Nadp+ and Jf0048
- 4xzi: Crystal Structure of Human Aldose Reductase Complexed with Nadp+ and Jf0049
- 6tuc: Human Aldose Reductase in Complex with Alr25
- 6tuf: Human Aldose Reductase in Complex with Alr43
- 6txp: Human Aldose Reductase Mutant L300A in Complex with a Ligand with an Idd Structure (3-({[2-(carboxymethoxy)-4-fluorobenzoyl]amino}methyl) Benzoic Acid)
- 6xum: Human Aldose Reductase Mutant L300/301a in Complex with a Ligand with an Idd Structure ({5-fluoro-2-[(3-nitrobenzyl) Carbamoyl]phenoxy}acetic Acid)
- 6y03: Structure of Human Aldose Reductase Mutant L300/301a with a Citrate Molecule Bound in The Anion Binding Pocket
- 6y1p: Human Aldose Reductase Mutant L300/301a in Complex with a Ligand with an Idd Structure (3-({[2-(carboxymethoxy)-4- Fluorobenzoyl]amino}methyl)benzoic Acid)
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