|
79
|
257
|
3s8xA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4-methyl-6-oxo-1,6-dihydro-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
157
|
405
|
6e9pB |
Crystal structure of tryptophan synthase from m. tuberculosis - open form with brd0059 bound |
|
76
|
257
|
5sz5A |
Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide |
|
81
|
257
|
5sz4A |
Carbonic anhydrase ix-mimic in complex with 4-(phenyl)-benzenesulfonamide |
|
64
|
266
|
5ku6A |
Crystal structure for the complex of human carbonic anhydrase iv and methazolamide |
|
64
|
266
|
5jnaA |
Crystal structure for the complex of human carbonic anhydrase iv and topiramate |
|
77
|
257
|
5jn7A |
Carbonic anhydrase ii in complex with u-ch3 |
|
79
|
257
|
5jn3A |
Carbonic anhydrase ix-mimic in complex with u-f |
|
64
|
266
|
5jn8A |
Crystal structure for the complex of human carbonic anhydrase iv and acetazolamide |
|
77
|
257
|
5jn1A |
Carbonic anhydrase ix-mimic in complex with u-ch3 |
|
82
|
257
|
5jmzA |
Carbonic anhydrase ix-mimic in complex with u-no2 |
|
63
|
266
|
5jn9A |
Crystal structure for the complex of human carbonic anhydrase iv and ethoxyzolamide |
|
67
|
266
|
5jncA |
Crystal structure for the complex of human carbonic anhydrase iv and 4-aminomethylbenzene sulfonamide |
|
127
|
306
|
5imiA |
Crystal structure of s303a aspergillus terreus aristolochene synthase complexed with (1s,8s,9ar)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
163
|
436
|
5idzA |
Structure of human enolase 2 in complex with (s)-(1-hydroxy-2-oxopiperidin-3-yl)phosphonate |
|
154
|
405
|
6du1B |
Crystal structure of tryptophan synthase from m. tuberculosis - open form with brd6309 bound |
|
92
|
260
|
6dweA |
Crystal structure of tryptophan synthase from m. tuberculosis - aminoacrylate- and brd0059-bound form |
|
122
|
342
|
6dxsA |
Crystal structure of the ligj hydratase e284q mutant substrate complex with (3z)-2-keto-4-carboxy-3-hexenedioate |
|
272
|
726
|
6dnpA |
Crystal structure of mycobacterium tuberculosis malate synthase in complex with 2-f-3-methyl-6-f-phenyldiketoacid |
|
275
|
726
|
6dl9A |
Crystal structure of mycobacterium tuberculosis malate synthase in complex with 2,6-cl-phenyldiketoacid |
|
275
|
726
|
6dkoA |
Crystal structure of mycobacterium tuberculosis malate synthase in complex with 2,6-f-phenyldiketoacid |
|
154
|
404
|
6duaB |
Crystal structure of tryptophan synthase from m. tuberculosis - aminoacrylate- and brd6309-bound form |
|
160
|
404
|
6dweB |
Crystal structure of tryptophan synthase from m. tuberculosis - aminoacrylate- and brd0059-bound form |
|
93
|
260
|
6e9pA |
Crystal structure of tryptophan synthase from m. tuberculosis - open form with brd0059 bound |
|
269
|
726
|
6dljA |
Crystal structure of mycobacterium tuberculosis malate synthase in complex with 2-nitro-phenyldiketoacid |
|
89
|
260
|
6du1A |
Crystal structure of tryptophan synthase from m. tuberculosis - open form with brd6309 bound |
|
89
|
260
|
6duaA |
Crystal structure of tryptophan synthase from m. tuberculosis - aminoacrylate- and brd6309-bound form |
|
77
|
259
|
6d1mA |
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects |
|
77
|
259
|
6d1lA |
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects |
|
76
|
259
|
6cehA |
Design, synthesis, x-ray and biological activities of selenides bearing the benzenesulfonamide moiety as new class of agents for prevention of diabetic cerebrovascular pathology |
|
13
|
81
|
6bm7A |
Crystal structure of trypanosoma brucei adometdc/prozyme heterodimer in complex with pyrimidineamine inhibitor utsam568 |
|
76
|
322
|
6bm7E |
Crystal structure of trypanosoma brucei adometdc/prozyme heterodimer in complex with pyrimidineamine inhibitor utsam568 |
|
67
|
270
|
6bm7B |
Crystal structure of trypanosoma brucei adometdc/prozyme heterodimer in complex with pyrimidineamine inhibitor utsam568 |
|
73
|
257
|
6bc9A |
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with dorzolamide |
|
75
|
257
|
6bccA |
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with ethoxzolamide |
|
61
|
257
|
6bbsA |
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with brinzolamide |
|
79
|
258
|
5vgyA |
Identification of a new zinc binding chemotype by fragment screening |
|
160
|
427
|
5dqlA |
Crystal structure of 2-vinyl glyoxylate modified isocitrate lyase from mycobacterium tuberculosis |
|
22
|
127
|
5bwaB |
Crystal structure of odc-plp-az1 ternary complex |
|
95
|
392
|
5bwaA |
Crystal structure of odc-plp-az1 ternary complex |
|
94
|
268
|
5bw6A |
Tryptophan synthase from salmonella typhimurium in complex with a single molecule of 2-({[4-(trifluoromethoxy)phenyl]carbonyl}amino)ethyl dihydrogen phosphate (f6) in the alpha-site. |
|
29
|
125
|
4zgyB |
Structure of human ornithine decarboxylase in complex with a c-terminal fragment of antizyme |
|
112
|
403
|
4zgyA |
Structure of human ornithine decarboxylase in complex with a c-terminal fragment of antizyme |
|
76
|
257
|
4zwyA |
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor |
|
77
|
257
|
4zwzA |
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate inhibitor |
|
72
|
261
|
4qjwA |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor |
|
77
|
260
|
4qsjA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide |
|
158
|
393
|
4ht3B |
The crystal structure of salmonella typhimurium tryptophan synthase at 1.30a complexed with n-(4'-trifluoromethoxybenzenesulfonyl)-2-amino-1-ethylphosphate (f9) inhibitor in the alpha site, internal aldimine |
|
75
|
257
|
4e4aA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
74
|
257
|
4e3fA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
