|
33
|
114
|
4trfA |
Crystal structure of macrophage migration inhibitory factor in complex with n-(pyridin-3-ylmethyl)thioformamide |
|
92
|
378
|
4tmaB |
Crystal structure of gyrase bound to its inhibitor yacg |
|
9
|
47
|
4tmaI |
Crystal structure of gyrase bound to its inhibitor yacg |
|
38
|
113
|
4tyoA |
Ppiase in complex with a non-phosphate small molecule inhibitor. |
|
136
|
508
|
4tmaA |
Crystal structure of gyrase bound to its inhibitor yacg |
|
34
|
114
|
4pluA |
Crystal structure of macrophage migration inhibitory factor in complex with benzaldehyde |
|
34
|
114
|
4p01A |
Crystal structure analysis of macrophage migration inhibitory factor in complex with n-[(4-cyanophenyl)methyl]methanethioamide |
|
35
|
114
|
4oyqA |
(6-isothiocyanatohexyl)benzene inhibitor complexed with macrophage migration inhibitory factor |
|
32
|
113
|
4p0hA |
Crystal structure analysis of macrophage migration inhibitory factor in complex with dimethylformamide |
|
33
|
113
|
4pkkA |
Crystal structure of macrophage migration inhibitory factor in complex with furan-2-ylmethyl)imino methanethiol |
|
18
|
102
|
4nnrA |
Fkbp13-fk506 complex |
|
33
|
114
|
4osfA |
4-(2-isothiocyanatoethyl)phenol inhibitor complexed with macrophage migration inhibitory factor |
|
124
|
382
|
4lutA |
Alanine racemase [clostridium difficile 630] complex with cycloserine |
|
122
|
382
|
4lutB |
Alanine racemase [clostridium difficile 630] complex with cycloserine |
|
58
|
210
|
4lp0A |
Crystal structure of a topoisomerase atp inhibitor |
|
60
|
210
|
4lpbA |
Crystal structure of a topoisomerase atpase inhibitor |
|
60
|
210
|
4motA |
Structure of streptococcus pneumonia pare in complex with az13072886 |
|
61
|
210
|
4mb9A |
Structure of streptococcus pneumonia pare in complex with az13102335 |
|
62
|
210
|
4mbcA |
Structure of streptococcus pneumonia pare in complex with az13053807 |
|
40
|
131
|
4lhoA |
Crystal structure of fg41malonate semialdehyde decarboxylase inhibited by 3-bromopropiolate |
|
62
|
210
|
4k4oA |
The dna gyrase b atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor |
|
59
|
205
|
4kfgA |
The dna gyrase b atp binding domain of escherichia coli in complex with a small molecule inhibitor. |
|
62
|
210
|
4ksgA |
Dna gyrase atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor (4-[(1s,5r,6r)-6-amino-1-methyl-3-azabicyclo[3.2.0]hept-3-yl]-6-fluoro-n-methyl-2-[(2-methylpyrimidin-5-yl)oxy]-9h-pyrimido[4,5-b]indol-8-amine) |
|
59
|
210
|
4kshA |
Dna gyrase atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor (7-({4-[(3r)-3-aminopyrrolidin-1-yl]-5-chloro-6-ethyl-7h-pyrrolo[2,3-d]pyrimidin-2-yl}sulfanyl)-1,5-naphthyridin-1(4h)-ol) |
|
60
|
210
|
4ktnA |
Dna gyrase atp binding domain of enterococcus faecalis in complex with a small molecule inhibitor ((3s)-1-[2-(pyrido[2,3-b]pyrazin-7-ylsulfanyl)-9h-pyrimido[4,5-b]indol-4-yl]pyrrolidin-3-amine) |
|
50
|
164
|
4j5eX |
Human cyclophilin d complexed with an inhibitor |
|
57
|
164
|
4j5aX |
Human cyclophilin d complexed with an inhibitor |
|
34
|
122
|
4j4oA |
Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with d44 |
|
52
|
207
|
4hz5A |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity |
|
60
|
204
|
4hypA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
107
|
376
|
4hxzA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
109
|
371
|
4hy1A |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
56
|
203
|
4hz0A |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
59
|
210
|
4hxwA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
110
|
371
|
4hymA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
52
|
164
|
4j59A |
Human cyclophilin d complexed with an inhibitor |
|
28
|
123
|
4j4nA |
Crystal structure of fk506 binding domain of plasmodium falciparum fkbp35 in complex with d44 |
|
53
|
164
|
4j5bA |
Human cyclophilin d complexed with an inhibitor |
|
55
|
164
|
4j58A |
Human cyclophilin d complexed with an inhibitor |
|
47
|
164
|
4j5cX |
Human cyclophilin d complexed with an inhibitor |
|
53
|
164
|
4ipzA |
Smbz bound to cyclophilin a |
|
60
|
210
|
4gglA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity |
|
57
|
210
|
4gfnA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic |
|
59
|
210
|
4geeA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
|
143
|
416
|
4gaeA |
Crystal structure of plasmodium dxr in complex with a pyridine-containing inhibitor |
|
51
|
164
|
3r54A |
Human cyclophilin d complexed with a fragment |
|
52
|
164
|
3r59A |
Human cyclophilin d complexed with a fragment |
|
54
|
164
|
3r49A |
Human cyclophilin d complexed with quinolin-8-amine |
|
132
|
357
|
4fp1A |
P. putida mandelate racemase co-crystallized with 3,3,3-trifluoro-2-hydroxy-2-(trifluoromethyl) propionic acid |
|
54
|
164
|
3r4gA |
Human cyclophilin d complexed with a fragment |
