|
77
|
257
|
4mo8A |
The crystal structure of the human carbonic anhydrase ii in complex with n-[2-(2-methyl-5-nitro-1h-imidazol-1-yl)ethyl]sulfamide |
|
75
|
258
|
4mtyA |
Structure at 1a resolution of a helical aromatic foldamer-protein complex. |
|
84
|
212
|
4muzA |
Crystal structure of orotidine 5'-monophosphate decarboxylase from archaeoglobus fulgidus complexed with inhibitor bmp |
|
76
|
258
|
4mdlA |
Meta carborane carbonic anhydrase inhibitor |
|
110
|
293
|
4lzjA |
Crystal structure of murq from h.influenzae with bound inhibitor |
|
76
|
258
|
4mdgA |
Closo carborane carbonic anhydrase inhibitor |
|
81
|
258
|
4mdmA |
Nido-carborane carbonic anhydrase inhibitor |
|
132
|
304
|
4kvwA |
Crystal structure of aspergillus terreus aristolochene synthase complexed with (3r,6r,9ar)-6,9a-dimethyl-3-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
49
|
177
|
4kyhA |
Crystal structure of mouse glyoxalase i complexed with zopolrestat |
|
132
|
304
|
4kwdA |
Crystal structure of aspergillus terreus aristolochene synthase complexed with (1r,8r,9as)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
79
|
256
|
4kuvA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-chlorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |
|
130
|
304
|
4kvyA |
Crystal structure of aspergillus terreus aristolochene synthase complexed with (1s,8s,9ar)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
78
|
257
|
4kv0A |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-tosylureido)pyridine-2-sulfonamide inhibitor |
|
135
|
304
|
4kvdA |
Crystal structure of aspergillus terreus aristolochene synthase complexed with (4as,7s)-1,4a-dimethyl-7-(prop-1-en-2-yl)decahydroquinolin-1-ium |
|
51
|
179
|
4kykA |
Crystal structure of mouse glyoxalase i complexed with indomethacin |
|
75
|
261
|
4kp5A |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
|
48
|
142
|
4kijA |
Design and structural analysis of aromatic inhibitors of type ii dehydroquinase dehydratase from mycobacterium tuberculosis - compound 35c [3,4-dihydroxy-5-(3-nitrophenoxy)benzoic acid] |
|
78
|
259
|
4knmA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide |
|
76
|
257
|
4knjA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
|
162
|
395
|
4kkxB |
Crystal structure of tryptophan synthase from salmonella typhimurium with 2-aminophenol quinonoid in the beta site and the f6 inhibitor in the alpha site |
|
102
|
268
|
4kkxA |
Crystal structure of tryptophan synthase from salmonella typhimurium with 2-aminophenol quinonoid in the beta site and the f6 inhibitor in the alpha site |
|
45
|
141
|
4ki7A |
Design and structural analysis of aromatic inhibitors of type ii dehydroquinase from mycobacterium tuberculosis - compound 41c [3-hydroxy-5-(3-nitrophenoxy)benzoic acid] |
|
71
|
261
|
4kp8A |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
|
78
|
258
|
4knnA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
|
51
|
141
|
4kiuA |
Design and structural analysis of aromatic inhibitors of type ii dehydroquinate dehydratase from mycobacterium tuberculosis - compound 49d [5-[(3-nitrobenzyl)oxy]benzene-1,3-dicarboxylic acid] |
|
48
|
141
|
4kiwA |
Design and structural analysis of aromatic inhibitors of type ii dehydroquinate dehydratase from mycobacterium tuberculosis - compound 49e [5-[(3-nitrobenzyl)amino]benzene-1,3-dicarboxylic acid] |
|
84
|
222
|
4lc8A |
Crystal structure of the mutant h128n of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
76
|
257
|
4lhiA |
Crystal structure of human carbonic anhydrase isozyme ii with 5-(phenylsulfonyl)thiophene-2-sulfonamide |
|
85
|
222
|
4lc6A |
Crystal structure of the mutant h128q of orotidine 5'-monophosphate decarboxylase from methanobacterium thermoautotrophicum complexed with the inhibitor bmp |
|
76
|
257
|
4kniA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide |
|
80
|
257
|
4kuwA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-fluorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |
|
79
|
257
|
4kuyA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(o-tolylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |
|
133
|
304
|
4kviA |
Crystal structure of aspergillus terreus aristolochene synthase complexed with (4as,7s)-4a-methyl-7-(prop-1-en-2-yl)-2,3,4,4a,5,6,7,8-octahydroquinolin-1-ium |
|
78
|
257
|
4iwzA |
Structure of hcaii in complex with an acetazolamide derivative |
|
81
|
302
|
4iygA |
Structure of strictosidine synthase in complex with 2-(1h-indol-3-yl)-n-methylethanamine |
|
77
|
257
|
4itpA |
Structure of human carbonic anhydrase ii bound to a benzene sulfonamide |
|
75
|
257
|
4itoA |
Human ca ii inhibition by novel sulfonamide |
|
80
|
301
|
4imbA |
Structure of strictosidine synthase in complex with 2-(1-methyl-1h-indol-3-yl)ethanamine |
|
76
|
257
|
4ilxA |
Structure of human carbonic anhydrase ii in complex with an adamantyl sulfonamide inhibitor |
|
76
|
257
|
4jsaA |
Benzenesulfonamide complexed with hcaii h94d |
|
76
|
257
|
4jssA |
Human carbonic anhydrase ii h94d bound to a bidentate inhibitor |
|
74
|
257
|
4jswA |
Human carbonic anhydrase ii h94c |
|
75
|
257
|
4jszA |
Benzenesulfonamide bound to hcaii h94c |
|
103
|
268
|
4hpxA |
Crystal structure of tryptophan synthase at 1.65 a resolution in complex with alpha aminoacrylate e(a-a) and benzimidazole in the beta site and the f9 inhibitor in the alpha site |
|
162
|
395
|
4hpjB |
Crystal structure of tryptophan synthase at 1.45 a resolution in complex with 2-aminophenol quinonoid in the beta site and the f9 inhibitor in the alpha site |
|
161
|
395
|
4hpxB |
Crystal structure of tryptophan synthase at 1.65 a resolution in complex with alpha aminoacrylate e(a-a) and benzimidazole in the beta site and the f9 inhibitor in the alpha site |
|
103
|
268
|
4hn4A |
Tryptophan synthase in complex with alpha aminoacrylate e(a-a) form and the f9 inhibitor in the alpha site |
|
163
|
395
|
4hn4B |
Tryptophan synthase in complex with alpha aminoacrylate e(a-a) form and the f9 inhibitor in the alpha site |
|
79
|
259
|
4hu1A |
Crystal structure of human carbonic anhydrase isozyme xiii with the inhibitor. |
|
77
|
257
|
4ht0A |
Crystal structure of human carbonic anhydrase isozyme ii with the inhibitor. |
