|
28
|
123
|
4j4nA |
Crystal structure of fk506 binding domain of plasmodium falciparum fkbp35 in complex with d44 |
|
47
|
164
|
4j5cX |
Human cyclophilin d complexed with an inhibitor |
|
52
|
164
|
4j5dX |
Human cyclophilin d complexed with an inhibitor |
|
28
|
107
|
4ipxA |
Analyzing the visible conformational substates of the fk506 binding protein fkbp12 |
|
53
|
164
|
4j5bA |
Human cyclophilin d complexed with an inhibitor |
|
33
|
121
|
4itzA |
Crystal structure of the fk506 binding domain of plasmodium vivax fkbp35 in complex with a tetrapeptide substrate |
|
4
|
33
|
4gwtA |
Structure of racemic pin1 ww domain cocrystallized with dl-malic acid |
|
4
|
33
|
4gwvA |
Structure of racemic pin1 ww domain cocrystallized with tri-ammonium citrate |
|
48
|
191
|
4ggqA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed with cj40 |
|
46
|
191
|
4g50A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj168 |
|
48
|
192
|
4givA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj183 |
|
50
|
185
|
4frvA |
Crystal structure of mutated cyclophilin b that causes hyperelastosis cutis in the american quarter horse |
|
47
|
185
|
4fruA |
Crystal structure of horse wild-type cyclophilin b |
|
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 |
|
44
|
190
|
4fn2A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj37 |
|
54
|
164
|
3r4gA |
Human cyclophilin d complexed with a fragment |
|
54
|
164
|
3r56A |
Human cyclophilin d complexed with a fragment |
|
53
|
164
|
3r57A |
Human cyclophilin d complexed with a fragment |
|
52
|
164
|
3qyuA |
Crystal structure of human cyclophilin d at 1.54 a resolution at room temperature |
|
51
|
163
|
3pmpA |
Crystal structure of cyclophilin a from moniliophthora perniciosa in complex with cyclosporin a |
|
53
|
223
|
3prbA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
|
30
|
124
|
3pa7A |
Crystal structure of fkbp from plasmodium vivax in complex with tetrapeptide alpf |
|
38
|
150
|
3pr9A |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
|
33
|
150
|
3praA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
|
36
|
223
|
3prdA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
|
42
|
157
|
3odkA |
Discovery of cell-active phenyl-imidazole pin1 inhibitors by structure-guided fragment evolution |
|
49
|
158
|
3oobA |
Structural and functional insights of directly targeting pin1 by epigallocatechin-3-gallate |
|
35
|
127
|
3o5mA |
Fk1 domain mutant a19t of fkbp51, crystal form ii |
|
35
|
128
|
3o5pA |
Fk1 domain mutant a19t of fkbp51, crystal form iv |
|
36
|
128
|
3o5gA |
Fk1 domain of fkbp51, crystal form i |
|
34
|
128
|
3o5oA |
Fk1 domain mutant a19t of fkbp51, crystal form iii |
|
53
|
165
|
3odlA |
Crystal structure of cyclophilin a in complex with voclosporin z-isa247 |
|
34
|
125
|
3o5fA |
Fk1 domain of fkbp51, crystal form vii |
|
33
|
128
|
3o5rA |
Complex of fk506 with the fk1 domain mutant a19t of fkbp51 |
|
31
|
124
|
3o5jA |
Fk1 domain of fkbp51, crystal form iii |
|
54
|
165
|
3odiA |
Crystal structure of cyclophilin a in complex with voclosporin e-isa247 |
|
55
|
242
|
3o5dA |
Crystal structure of a fragment of fkbp51 comprising the fk1 and fk2 domains |
|
31
|
127
|
3o5kA |
Fk1 domain of fkbp51, crystal form viii |
|
31
|
128
|
3o5eA |
Fk1 domain of fkbp51, crystal form vi |
|
36
|
128
|
3o5iA |
Fk1 domain of fkbp51, crystal form ii |
|
36
|
128
|
3o5qA |
Fk1 domain mutant a19t of fkbp51, crystal form iv, in presence of dmso |
|
38
|
128
|
3o5lA |
Fk1 domain mutant a19t of fkbp51, crystal form i |
|
46
|
158
|
3ntpA |
Human pin1 complexed with reduced amide inhibitor |
|
27
|
109
|
3mdyB |
Crystal structure of the cytoplasmic domain of the bone morphogenetic protein receptor type-1b (bmpr1b) in complex with fkbp12 and ldn-193189 |
|
16
|
83
|
3mdfA |
Crystal structure of the rrm domain of cyclophilin 33 |
|
13
|
79
|
3lpyA |
Crystal structure of the rrm domain of cyp33 |
|
28
|
151
|
3luoA |
Crystal structure and functional characterization of the thermophilic prolyl isomerase and chaperone slyd |
|
25
|
119
|
3kz7A |
C-terminal domain of murine fkbp25 rapamycin complex |
