|
118
|
327
|
4dptA |
Crystal structure of staphylococcus epidermidis mevalonate diphosphate decarboxylase complexed with inhibitor 6-fmvapp and atpgs |
|
73
|
257
|
4dz7A |
Hca ii in complex with novel sulfonamide inhibitors set d |
|
75
|
257
|
4dz9A |
Hca ii in complex with novel sulfonamide inhibitors set d |
|
216
|
535
|
4di5A |
Co-crystal structure of wt 5-epi-aristolochene synthase from nicotiana tobaccum with geraniline |
|
116
|
330
|
4du8A |
Crystal structure of staphylococcus epidermidis d283a mevalonate diphosphate decarboxylase complexed with inhibitor dpgp |
|
119
|
330
|
4dpuA |
Crystal structure of staphylococcus epidermidis s192a mevalonate diphosphate decarboxylase complexed with inhibitor 6-fmvapp and atpgs |
|
122
|
330
|
4dpyA |
Crystal structure of staphylococcus epidermidis s192a mevalonate diphosphate decarboxylase complexed with inhibitor dpgp |
|
78
|
257
|
4e49A |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
75
|
257
|
4e3gA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
76
|
257
|
4e3dA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
77
|
257
|
4e3hA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
70
|
199
|
4df1A |
Crystal structure of orotidine 5'-monophosphate decarboxylase from thermoproteus neutrophilus complexed with inhibitor bmp |
|
81
|
213
|
4dbeA |
Crystal structure of orotidine 5'-monophosphate decarboxylase from sulfolobus solfataricus complexed with inhibitor bmp |
|
122
|
299
|
4bs0A |
Crystal structure of kemp eliminase hg3.17 e47n,n300d complexed with transition state analog 6-nitrobenzotriazole |
|
49
|
176
|
3w0tA |
Human glyoxalase i with an n-hydroxypyridone derivative inhibitor |
|
46
|
175
|
3w0uA |
Human glyoxalase i with an n-hydroxypyridone inhibitor |
|
48
|
176
|
3vw9A |
Human glyoxalase i with an n-hydroxypyridone inhibitor |
|
87
|
247
|
3uz5A |
Designed protein ke59 r13 3/11h |
|
78
|
258
|
3v7xA |
Complex of human carbonic anhydrase ii with n-[2-(3,4-dimethoxyphenyl)ethyl]-4-sulfamoylbenzamide |
|
76
|
257
|
3v5gA |
Crystal structure of human carbonic anhydrase ii in complex with the 4-sulfamido-benzenesulfonamide inhibitor |
|
83
|
220
|
3v1pA |
Crystal structure of the mutant q185a of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
79
|
206
|
3ve7A |
Crystal structure of orotidine 5'-monophosphate decarboxylase from metallosphaera sedula complexed with inhibitor bmp |
|
108
|
318
|
3vi2A |
Crystal structure analysis of plasmodium falciparum omp decarboxylase in complex with inhibitor hmoa |
|
79
|
258
|
3vbdA |
Complex of human carbonic anhydrase ii with 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide |
|
94
|
248
|
3ud6A |
Structural analyses of covalent enzyme-substrate analogue complexes reveal strengths and limitations of de novo enzyme design |
|
75
|
222
|
3ucnA |
Coccomyxa beta-carbonic anhydrase in complex with azide |
|
75
|
222
|
3ucjA |
Coccomyxa beta-carbonic anhydrase in complex with acetazolamide |
|
98
|
247
|
3uxdA |
Designed protein ke59 r1 7/10h with dichlorobenzotriazole (dbt) |
|
73
|
222
|
3ucmA |
Coccomyxa beta-carbonic anhydrase in complex with thiocyanate |
|
75
|
222
|
3ucoA |
Coccomyxa beta-carbonic anhydrase in complex with iodide |
|
73
|
222
|
3uckA |
Coccomyxa beta-carbonic anhydrase in complex with phosphate |
|
91
|
247
|
3uzjA |
Designed protein ke59 r13 3/11h with benzotriazole |
|
77
|
257
|
3t83A |
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates |
|
80
|
256
|
3t5uA |
Crystal structure of the human carbonic anhydrase ii in complex with n-hydroxy benzenesulfonamide |
|
75
|
257
|
3t82A |
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates |
|
75
|
257
|
3t84A |
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates |
|
73
|
257
|
3t85A |
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates |
|
106
|
281
|
3t88A |
Crystal structure of escherichia coli menb in complex with substrate analogue, osb-ncoa |
|
95
|
279
|
3t8aA |
Crystal structure of mycobacterium tuberculosis menb in complex with substrate analogue, osb-ncoa |
|
74
|
258
|
3t5zA |
Crystal structure of the human carbonic anhydrase ii in complex with n-methoxy-benzenesulfonamide |
|
83
|
220
|
3sj3A |
Crystal structure of the mutant r160a.y206f of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
84
|
219
|
3sizA |
Crystal structure of the mutant s127a of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
78
|
259
|
3sbhA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
85
|
214
|
3secA |
Crystal structure of methanothermobacter thermautotrophicus orotidine 5'-monophosphate decarboxylase complexed with pyrazofurin monophosphate |
|
79
|
258
|
3saxA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(5-ethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
77
|
258
|
3sbiA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-[(2-pyrimidinylsulfanyl)acetyl]benzenesulfonamide |
|
75
|
257
|
3sapA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(5-butyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
86
|
220
|
3rlvA |
Crystal structure of the mutant y206f of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
83
|
220
|
3rluA |
Crystal structure of the mutant k82a of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
78
|
258
|
3rj7A |
Human carbonic anhydrase ii complexed with its inhibitor rhenium(i)triscarbonyl-cyclopentadienyl-carboxy-4-aminomethylbenzene-sulfonamide |
