|
58
|
191
|
5xdsA |
Crystal structure of mycobacterium tuberculosis hisb bound with an inhibitor |
|
78
|
258
|
5wexA |
Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors |
|
70
|
302
|
5tz6A |
Crystal structure of curj dehydratase h978f inactive mutant in complex with compound 21 |
|
77
|
257
|
5thnA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-triene-1-thione bound to human carbonic anhydrase 2 |
|
76
|
257
|
5th4A |
Crystal structure of 1-hydroxypyridine-2(1h)-thione bound to human carbonic anhydrase 2 l198g |
|
147
|
433
|
5tijA |
Structure of human enolase 2 with ((3s,5s)-1,5-dihydroxy-3-methyl-2-oxopyrrolidin-3-yl)phosphonate (purified enantiomer) |
|
76
|
257
|
5ti0A |
Crystal structure of 2-hydroxycyclohepta-2,4,6-triene-1-thione bound to human carbonic anhydrase 2 l198g |
|
38
|
226
|
5tv3A |
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with (e)-5-(((4-(tert-butyl)phenyl)sulfonyl)imino)-4-methyl-4,5-dihydro-1,3,4-thiadiazole-2-sulfonamide |
|
51
|
227
|
5tuoA |
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor. |
|
75
|
258
|
5tfxA |
New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase |
|
79
|
257
|
5thiA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 l198g |
|
78
|
257
|
5thjA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 |
|
81
|
257
|
5sz7A |
Carbonic anhydrase ix-mimic in complex with 4-(3-quinolinyl)-benzenesulfonamide |
|
77
|
257
|
5sz2A |
Carbonic anhydrase ii in complex with 4-(3-formylphenyl)-benzenesulfonamide |
|
78
|
257
|
5sz1A |
Carbonic anhydrase ii in complex with 4-(2-methylphenyl)-benzenesulfonamide |
|
79
|
257
|
5sz3A |
Carbonic anhydrase ii in complex with 4-(3-quinolinyl)-benzenesulfonamide |
|
78
|
257
|
5sz0A |
Carbonic anhydrase ii in complex with 4-(phenyl)-benzenesulfonamide |
|
76
|
257
|
5sz6A |
Carbonic anhydrase ix-mimic in complex with 4-(3-formylphenyl)-benzenesulfonamide |
|
153
|
395
|
5bw6B |
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. |
|
129
|
305
|
5ivgA |
Crystal structure of aspergillus terreus aristolochene synthase n299a complexed with farnesyl thiolodiphosphate |
|
132
|
304
|
5impA |
Crystal structure of n299a aspergillus terreus aristolochene synthase complexed with (1s,8s,9ar)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
125
|
304
|
5imnA |
Crystal structure of n299a/s303a aspergillus terreus aristolochene synthase complexed with (1s,8s,9ar)-1,9a-dimethyl-8-(prop-1-en-2-yl)decahydroquinolizin-5-ium |
|
80
|
257
|
4zx1A |
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate inhibitor |
|
75
|
257
|
4zwxA |
Engineered carbonic anhydrase ix mimic in complex with glucosyl sulfamate inhibitor |
|
80
|
257
|
4zx0A |
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor |
|
175
|
433
|
4zcwA |
Structure of human enolase 2 in complex with sf2312 |
|
77
|
257
|
4zwiA |
Surface lysine acetylated human carbonic anhydrase ii in complex with a sulfamate-based inhibitor |
|
123
|
324
|
5f2mA |
Tagatose-1,6-bisphosphate aldolase from streptococcus pyogenes in complex with competitive inhibitor hexitol-1,6-bisphosphate |
|
176
|
459
|
5f91A |
Fumarate hydratase of mycobacterium tuberculosis in complex with formate and allosteric modulator (n-(5-(azepan-1-ylsulfonyl)-2-methoxyphenyl)-2-(4-oxo-3,4-dihydrophthalazin-1-yl)acetamide) |
|
73
|
257
|
5eijA |
Carbonic anhydrase ii in complex with sulfonamide inhibitor |
|
168
|
433
|
5eu9A |
Structure of human enolase 2 in complex with ((3s,5s)-1,5-dihydroxy-3-methyl-2-oxopyrrolidin-3-yl)phosphonic acid |
|
119
|
297
|
5f1uA |
Biomimetic design results in a potent allosteric inhibitor of dihydrodipicolinate synthase from campylobacter jejuni |
|
121
|
296
|
5f1vA |
Biomimetic design results in a potent allosteric inhibitor of dihydrodipicolinate synthase from campylobacter jejuni |
|
76
|
257
|
5ekhA |
Human carbonic anhydrase ii complexed with a two-faced guest |
|
77
|
257
|
5ekmA |
Human carbonic anhydrase ii complexed with a two-faced guest |
|
77
|
258
|
5ekjA |
Human carbonic anhydrase ii complexed with a two-faced guest |
|
169
|
434
|
4za0A |
Structure of human enolase 2 in complex with phosphonoacetohydroxamate |
|
159
|
396
|
4zqcB |
Tryptophan synthase from salmonella typhimurium in complex with two molecules of n-(4'-trifluoromethoxybenzoyl)-2-amino-1-ethylphosphate (f6f) inhibitor in the alpha-site and a single f6f molecule in the beta-site at 1.54 angstrom resolution. |
|
101
|
268
|
4zqcA |
Tryptophan synthase from salmonella typhimurium in complex with two molecules of n-(4'-trifluoromethoxybenzoyl)-2-amino-1-ethylphosphate (f6f) inhibitor in the alpha-site and a single f6f molecule in the beta-site at 1.54 angstrom resolution. |
|
159
|
509
|
5cwaA |
Structure of anthranilate synthase component i (trpe) from mycobacterium tuberculosis with inhibitor bound |
|
154
|
390
|
5cgqB |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with f9 ligand in the alpha-site and the product l-tryptophan in the beta-site. |
|
101
|
268
|
5cgqA |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with f9 ligand in the alpha-site and the product l-tryptophan in the beta-site. |
|
152
|
394
|
4xugB |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with 2-({[4-(trifluoromethoxy)phenyl]sulfonyl}amino)ethyl dihydrogen phosphate (f9f) inhibitor in the alpha site and ammonium ion in the metal coordination site. |
|
96
|
268
|
4y6gA |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with n-(4'-trifluoromethoxybenzoyl)-2-amino-1-ethylphosphate (f6f) inhibitor in the alpha-site and beta-site. |
|
154
|
396
|
4y6gB |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with n-(4'-trifluoromethoxybenzoyl)-2-amino-1-ethylphosphate (f6f) inhibitor in the alpha-site and beta-site. |
|
101
|
267
|
4xugA |
Crystal structure of tryptophan synthase from salmonella typhimurium in complex with 2-({[4-(trifluoromethoxy)phenyl]sulfonyl}amino)ethyl dihydrogen phosphate (f9f) inhibitor in the alpha site and ammonium ion in the metal coordination site. |
|
43
|
167
|
4x2aA |
Crystal structure of mouse glyoxalase i complexed with baicalein |
|
1
|
10
|
4tr9E |
Ternary co-crystal structure of fructose-bisphosphate aldolase from plasmodium falciparum in complex with trap and a small molecule inhibitor |
|
1
|
11
|
4tr9G |
Ternary co-crystal structure of fructose-bisphosphate aldolase from plasmodium falciparum in complex with trap and a small molecule inhibitor |
|
125
|
347
|
4tr9A |
Ternary co-crystal structure of fructose-bisphosphate aldolase from plasmodium falciparum in complex with trap and a small molecule inhibitor |
