|
47
|
157
|
3tc5A |
Selective targeting of disease-relevant protein binding domains by o-phosphorylated natural product derivatives |
|
142
|
436
|
3st6A |
Structure of a m. tuberculosis synthase, mbti, in complex with an isochorismate analogue inhibitor |
|
34
|
114
|
3smbA |
Phenethylisothiocyanate covalently bound to macrophage migration inhibitory factor (mif) |
|
33
|
114
|
3smcA |
Macrophage migration inhibitory factor (mif) with covalently bound l-sulforaphane |
|
54
|
158
|
3sgwA |
Crystal structure of ribose-5-phosphate isomerase b rpib from coccidioides immitis semi-covalently bound to malonic acid |
|
133
|
436
|
3rv9A |
Structure of a m. tuberculosis salicylate synthase, mbti, in complex with an inhibitor with ethyl r-group |
|
129
|
436
|
3rv8A |
Structure of a m. tuberculosis salicylate synthase, mbti, in complex with an inhibitor with cyclopropyl r-group |
|
134
|
436
|
3rv6A |
Structure of a m. tuberculosis salicylate synthase, mbti, in complex with an inhibitor with phenyl r-group |
|
128
|
435
|
3rv7A |
Structure of a m. tuberculosis salicylate synthase, mbti, in complex with an inhibitor with isopropyl r-group |
|
53
|
164
|
3rd9X |
Human cyclophilin d complexed with a fragment |
|
53
|
164
|
3rddA |
Human cyclophilin a complexed with an inhibitor |
|
51
|
164
|
3rdcA |
Human cyclophilin d complexed with an inhibitor |
|
52
|
164
|
3rdbA |
Human cyclophilin d complexed with a fragment |
|
56
|
164
|
3rdaX |
Human cyclophilin d complexed with a fragment |
|
56
|
164
|
3rckX |
Human cyclophilin d complexed with a fragment |
|
57
|
164
|
3rciX |
Human cyclophilin d complexed with 5-methyl-1,2-oxazol-3-amine |
|
46
|
164
|
3rcgA |
Human cyclophilin d complexed with dimethylformamide |
|
33
|
116
|
3rf5A |
Ancylostoma ceylanicum mif in complex with n-(2,3,4,5,6-pentafluoro-benzyl)-4-sulfamoyl-benzamide |
|
33
|
116
|
3rf4A |
Ancylostoma ceylanicum mif in complex with furosemide |
|
55
|
164
|
3rcfA |
Human cyclophilin d complexed with n-[(4-aminophenyl)sulfonyl]benzamide |
|
55
|
164
|
3rclA |
Human cyclophilin d complexed with a fragment |
|
148
|
533
|
5ulgA |
Crystal structure of rpe65 in complex with mb-008 and palmitate |
|
151
|
533
|
5ul5A |
Crystal structure of rpe65 in complex with mb-004 and palmitate |
|
15
|
62
|
5tigA |
Crystal structure of 4-oxalocrotonate tautomerase inactivated by brhpd |
|
53
|
164
|
5t9wA |
Discovery of a potent cyclophilin inhibitor (compound 5) based on structural simplification of sanglifehrin a |
|
53
|
163
|
5t9uA |
Discovery of a potent cyclophilin inhibitor (compound 3) based on structural simplification of sanglifehrin a |
|
52
|
163
|
5ta2A |
Discovery of a potent cyclophilin inhibitor (compound 7) based on structural simplification of sanglifehrin a |
|
53
|
164
|
5ta4A |
Discovery of a potent cyclophilin inhibitor (compound 8) based on structural simplification of sanglifehrin a |
|
51
|
163
|
5t9zA |
Discovery of a potent cyclophilin inhibitor (compound 6) based on structural simplification of sanglifehrin a |
|
60
|
210
|
5bocA |
Crystal structure of topoisomerase pare inhibitor |
|
36
|
114
|
5j7qA |
Macrophage migration inhibitory factor bound to inhibitor k664 derivative |
|
33
|
114
|
5j7pA |
Macrophage migration inhibitory factor bound to covalent inhibitor rdr03785 |
|
64
|
148
|
5bqgA |
Crystal structure of mpges-1 bound to an inhibitor |
|
69
|
193
|
5d7rA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a ligand |
|
63
|
192
|
5d6qA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a ligand |
|
61
|
192
|
5d6pA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a ligand |
|
65
|
192
|
5d7cA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a ligand |
|
66
|
193
|
5d7dA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a ligand |
|
65
|
148
|
4yl1A |
Crystal structures of mpges-1 inhibitor complexes |
|
63
|
192
|
5cphA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a fragment |
|
65
|
192
|
5ctyA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a fragment |
|
65
|
192
|
5ctxA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a fragment |
|
60
|
192
|
5ctwA |
Crystal structure of the atp binding domain of s. aureus gyrb complexed with a fragment |
|
63
|
146
|
4yl3A |
Crystal structures of mpges-1 inhibitor complexes |
|
64
|
148
|
4yl0A |
Crystal structures of mpges-1 inhibitor complexes |
|
64
|
146
|
4yk5A |
Crystal structures of mpges-1 inhibitor complexes |
|
123
|
386
|
4xgkA |
Crystal strucutre of udp-galactopyranose mutase from corynebacterium diphtheriae in complex with 2-[4-(4-chlorophenyl)-7-(2-thienyl)-2-thia-5,6,8,9-tetrazabicyclo[4.3.0]nona-4,7,9-trien-3-yl]acetic |
|
117
|
357
|
4xbjA |
Y274f alanine racemase from e. coli inhibited by l-ala-p |
|
32
|
114
|
4wr8A |
Macrophage migration inhibitory factor in complex with a biaryltriazole inhibitor (3b-180) |
|
36
|
114
|
4wrbA |
Macrophage migration inhibitory factor in complex with a biaryltriazole inhibitor (3b-190) |
