|
110
|
313
|
2fzdA |
Human aldose reductase complexed with tolrestat at 1.08 a resolution. |
|
108
|
316
|
2fzbA |
Human aldose reductase complexed with four tolrestat molecules at 1.5 a resolution. |
|
104
|
315
|
2fz8A |
Human aldose reductase complexed with inhibitor zopolrestat at 1.48 a(1 day soaking). |
|
113
|
323
|
2fvlA |
Crystal structure of human 3-alpha hydroxysteroid/dihydrodiol dehydrogenase (akr1c4) complexed with nadp+ |
|
103
|
315
|
2fz9A |
Human aldose reductase complexed with inhibitor zopolrestat after six days soaking. |
|
115
|
319
|
2f38A |
Crystal structure of prostaglandin f synathase containing bimatoprost |
|
97
|
315
|
2f2kA |
Aldose reductase tertiary complex with nadph and deg |
|
118
|
323
|
2fgbA |
Crystal structure of human 17bet a-hydroxysteroid dehydrogenase type 5 in complexes with peg and nadp |
|
104
|
315
|
2duzA |
Human aldose reductase complexed with inhibitor zopolrestat after 3 days soaking (3days_soaked_2) |
|
105
|
315
|
2duxA |
Crystal structure of human aldose reductase complexed with zopolrestat after 3 days soaking (3days_soaked_1) |
|
110
|
314
|
2dv0A |
Human aldose reductase complexed with zopolrestat after 6 days soaking(6days_soaked_2) |
|
114
|
323
|
2clpA |
Crystal structure of human aflatoxin b1 aldehyde reductase member 3 |
|
126
|
325
|
2c91A |
Mouse succinic semialdehyde reductase, akr7a5 |
|
110
|
308
|
2bgsA |
Holo aldose reductase from barley |
|
120
|
323
|
2bp1A |
Structure of the aflatoxin aldehyde reductase in complex with nadph |
|
109
|
312
|
2bgqA |
Apo aldose reductase from barley |
|
95
|
324
|
2alrA |
Aldehyde reductase |
|
102
|
315
|
2acrA |
An anion binding site in human aldose reductase: mechanistic implications for the binding of citrate, cacodylate, and glucose-6-phosphate |
|
110
|
316
|
2agtA |
Aldose reductase mutant leu 300 pro complexed with fidarestat |
|
99
|
314
|
2acsA |
An anion binding site in human aldose reductase: mechanistic implications for the binding of citrate, cacodylate, and glucose-6-phosphate |
|
102
|
315
|
2acuA |
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 |
|
120
|
326
|
2a79A |
Mammalian shaker kv1.2 potassium channel- beta subunit complex |
|
119
|
317
|
1zq5A |
Crystal structure of human androgenic 17beta-hydroxysteroid dehydrogenase type 5 in complexed with a potent inhibitor em1404 |
|
99
|
315
|
2acqA |
An anion binding site in human aldose reductase: mechanistic implications for the binding of citrate, cacodylate, and glucose-6-phosphate |
|
99
|
308
|
1zgdA |
Chalcone reductase complexed with nadp+ at 1.7 angstrom resolution |
|
120
|
323
|
1zsxA |
Crystal structure of human potassium channel kv beta-subunit (kcnab2) |
|
112
|
319
|
1z9aA |
Crystal structure of the asn-309 to asp mutant of candida tenuis xylose reductase (akr2b5) bound to nad+ |
|
112
|
317
|
1zuaX |
Crystal structure of akr1b10 complexed with nadp+ and tolrestat |
|
107
|
316
|
1z89A |
Human aldose reductase complexed with novel sulfonyl-pyridazinone inhibitor |
|
104
|
315
|
1z8aA |
Human aldose reductase complexed with novel sulfonyl-pyridazinone inhibitor |
|
113
|
316
|
1z3nA |
Human aldose reductase in complex with nadp+ and the inhibitor lidorestat at 1.04 angstrom |
|
103
|
298
|
1ynpA |
Aldo-keto reductase akr11c1 from bacillus halodurans (apo form) |
|
102
|
298
|
1ynqA |
Aldo-keto reductase akr11c1 from bacillus halodurans (holo form) |
|
105
|
319
|
1ye4A |
Crystal structure of the lys-274 to arg mutant of candida tenuis xylose reductase (akr2b5) bound to nad+ |
|
110
|
319
|
1ye6A |
Crystal structure of the lys-274 to arg mutant of candida tenuis xylose reductase (akr2b5) bound to nadp+ |
|
114
|
325
|
1xjbA |
Crystal structure of human type 3 3alpha-hydroxysteroid dehydrogenase in complex with nadp(h), citrate and acetate molecules |
|
98
|
315
|
1xgdA |
Apo r268a human aldose reductase |
|
108
|
316
|
1x97A |
Crystal structure of aldose reductase complexed with 2r4s (stereoisomer of fidarestat, 2s4s) |
|
104
|
316
|
1x98A |
Crystal structure of aldose reductase complexed with 2s4r (stereoisomer of fidarestat, 2s4s) |
|
118
|
319
|
1xf0A |
Crystal structure of human 17beta-hydroxysteroid dehydrogenase type 5 (akr1c3) complexed with delta4-androstene-3,17-dione and nadp |
|
111
|
316
|
1x96A |
Crystal structure of aldose reductase with citrates bound in the active site |
|
108
|
284
|
1vp5A |
Crystal structure of 2,5-diketo-d-gluconic acid reductase (tm1009) from thermotoga maritima at 2.40 a resolution |
|
97
|
281
|
1vbjA |
The crystal structure of prostaglandin f synthase from trypanosoma brucei |
|
110
|
313
|
1us0A |
Human aldose reductase in complex with nadp+ and the inhibitor idd594 at 0.66 angstrom |
|
90
|
297
|
1ur3M |
Crystal structure of the apo form of the e.coli ydhf protein |
|
104
|
316
|
1t40A |
Crystal structure of human aldose reductase complexed with nadp and idd552 at ph 5 |
|
112
|
316
|
1t41A |
Crystal structure of human aldose reductase complexed with nadp and idd552 |
|
118
|
319
|
1sm9A |
Crystal structure of an engineered k274rn276d double mutant of xylose reductase from candida tenuis optimized to utilize nad |
|
115
|
315
|
1s2aA |
Crystal structures of prostaglandin d2 11-ketoreductase in complex with the non-steroidal anti-inflammatory drugs flufenamic acid and indomethacin |
|
124
|
319
|
1ry8A |
Prostaglandin f synthase complexed with nadph and rutin |
