105
|
257
|
7otuA |
Human ompd-domain of umps in complex with 6-hydroxy-ump at 0.95 angstroms resolution, crystal 2 |
98
|
258
|
7ov0A |
Orotidine 5'-monophosphate decarboxylase-domain of human umps in resting state at 0.95 angstrom resolution |
261
|
755
|
7pk6A |
Providencia stuartii arginine decarboxylase (adc), stack structure |
149
|
366
|
7pd1A |
Crystal structure of the l-tyrosine-bound radical sam tyrosine lyase thih (2-iminoacetate synthase) from thermosinus carboxydivorans |
78
|
257
|
7orpAAA |
Crystal structure of human carbonic anhydrase ii in complex with 4-((2-hydroxy-3-((3,4,5-trimethoxyphenyl)tellanyl)propyl)selanyl)benzenesulfonamide |
92
|
256
|
7oqkA |
Human ompd-domain of umps in complex with substrate omp at 1.10 angstroms resolution, 15 minutes soaking |
252
|
755
|
7p9bA |
Providencia stuartii arginine decarboxylase (adc), decamer structure |
80
|
277
|
7oa1AAA |
Crystal structure of alfa carbonic anhydrase from schistosoma mansoni with 4-(2-(3-(4-iodophenyl)ureido)ethyl)benzenesulfonamide |
84
|
276
|
7o2sA |
Crystal structure of a tetrameric form of carbonic anhydrase from schistosoma mansoni |
88
|
278
|
7o48A |
Crystal structure of carbonic anhydrase from schistosoma mansoni with 4-(2-(3-(4-iodophenyl)thioureido)ethyl)benzenesulfonamide |
79
|
257
|
7nzsA |
Crystal structure of chimeric carbonic anhydrase va with 2,3,5,6-tetrafluoro-4-(propylsulfanyl)benzenesulfonamide |
79
|
257
|
7nzuA |
Crystal structure of chimeric carbonic anhydrase va with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
94
|
256
|
7oqiA |
Human ompd-domain of umps in complex with substrate omp at 1.15 angstrom resolution, 10 minutes soaking |
92
|
256
|
7oqnA |
Human ompd-domain of umps in complex with substrate omp at 1.10 angstroms resolution, 30 minutes soaking |
77
|
256
|
7nzrA |
Crystal structure of chimeric carbonic anhydrase va with 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)sulfanyl]benzenesulfonamide |
96
|
256
|
7oqiB |
Human ompd-domain of umps in complex with substrate omp at 1.15 angstrom resolution, 10 minutes soaking |
51
|
226
|
7o6hA |
Crystal structure of paradendryphiella salina pl7a alginate lyase mutant y223f in complex with tri-mannuronic acid |
91
|
256
|
7oqmA |
Human ompd-domain of umps in complex with substrate omp at 1.05 angstroms resolution, 20 minutes soaking |
98
|
256
|
7oqmB |
Human ompd-domain of umps in complex with substrate omp at 1.05 angstroms resolution, 20 minutes soaking |
52
|
226
|
7oryA |
Crystal structure of paradendryphiella salina pl7a alginate lyase in complex with penta-mannuronic acid products |
78
|
258
|
7nzxA |
Crystal structure of chimeric carbonic anhydrase va with 2,3,5,6-tetrafluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
93
|
256
|
7oqfA |
Human ompd-domain of umps in complex with omp at 1.05 angstrom resolution, 5 minutes soaking |
96
|
256
|
7oqnB |
Human ompd-domain of umps in complex with substrate omp at 1.10 angstroms resolution, 30 minutes soaking |
81
|
257
|
7nzwA |
Crystal structure of chimeric carbonic anhydrase va with 4-[(4,6-dimethylpyrimidin-2-yl)thio]-2,3,5,6-tetrafluorobenzenesulfonamide |
78
|
257
|
7orqAAA |
Crystal structure of human carbonic anhydrase ii in complex with 4-((3-(butylselanyl)-2-hydroxypropyl)selanyl)benzenesulfonamide |
99
|
256
|
7oqfB |
Human ompd-domain of umps in complex with omp at 1.05 angstrom resolution, 5 minutes soaking |
78
|
257
|
7nztA |
Crystal structure of chimeric carbonic anhydrase va with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
81
|
302
|
7mkuA |
Crystal structure of enoyl coa-hydratase2 from arabidopsis thaliana |
165
|
476
|
7eiwA |
Human histidine decarboxylase mutant y334f reacted with histidine |
124
|
392
|
7f1vB |
Crystal structure of pseudomonas putida methionine gamma-lyase q349s mutant with l-homocysteine intermediates |
136
|
396
|
7f1uA |
Crystal structure of pseudomonas putida methionine gamma-lyase q349s mutant with l-methionine intermediates |
120
|
392
|
7f1uB |
Crystal structure of pseudomonas putida methionine gamma-lyase q349s mutant with l-methionine intermediates |
169
|
475
|
7eiyA |
Human histidine decarboxylase mutant y334f soaking with histidine |
106
|
338
|
7f2yA |
Crystal structure of oxdb e85a mutant (form i) |
132
|
396
|
7f1vA |
Crystal structure of pseudomonas putida methionine gamma-lyase q349s mutant with l-homocysteine intermediates |
106
|
339
|
7f30A |
Crystal structure of oxdb e85a in complex with z-2- (3-bromophenyl) propanal oxime |
103
|
339
|
7f2zA |
Crystal structure of oxdb e85a mutant (form ii) |
169
|
476
|
7eixA |
Human histidine decarboxylase mutant y334f |
122
|
298
|
7bbvA |
Pectate lyase b from verticillium dahliae |
51
|
227
|
7p25A |
Crystal structure of paradendryphiella salina pl7a alginate lyase in complex with hexa-mannuronic acid products |
67
|
251
|
8q18A |
The crystal structure of human carbonic anhydrase ix in complex with sulfonamide |
192
|
568
|
8ej0A |
Crystal structure of fe-s cluster-dependent dehydratase from paralcaligenes ureilyticus in complex with mg |
163
|
502
|
8crdA |
Aspergillus niger ferulic acid decarboxylase (fdc) t40c-s315c (db1) variant in complex with prenylated flavin hydroxylated at the c1 prime position |
147
|
443
|
8ayfA |
Crystal structure of human sphingosine-1-phosphate lyase 1 |
106
|
383
|
8bb1A |
T3 sam lyase in complex with s-adenosylmethionine synthase |
60
|
240
|
8b04A |
Structure of porcine pancreatic elastase bound to a fragment of an isoxazolone inhibitor |
213
|
720
|
7vyvA |
Cryo-em structure of depo32, a klebsiella phage depolymerase targets the k2 serotype k. pneumoniae |
153
|
379
|
8bdqA |
Crystal structure of bacteroides ovatus cp926 pl38 alginate lyase |
33
|
153
|
8bb1E |
T3 sam lyase in complex with s-adenosylmethionine synthase |
385
|
1131
|
8e1uA |
Propionibacterium freudenreichii ppi-dependent pepck in complex with malate |