|
45
|
163
|
4dgcA |
Trimcyp cyclophilin domain from macaca mulatta: cyclosporin a complex |
|
24
|
108
|
4c02B |
Crystal structure of human acvr1 (alk2) in complex with fkbp12.6 and dorsomorphin |
|
15
|
98
|
4ca9A |
Structure of the nucleoplasmin-like n-terminal domain of drosophila fkbp39 |
|
21
|
117
|
4bf8A |
Fpr4 ppi domain |
|
46
|
157
|
3wh0A |
Structure of pin1 complex with 18-crown-6 |
|
46
|
191
|
3vawA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation v3i from burkholderia pseudomallei complexed with fk506 |
|
52
|
192
|
3uf8A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with a g95a surface mutation from burkholderia pseudomallei complexed with fk506 |
|
26
|
108
|
3uqiA |
Crystallographic structure of fkbp12 from aedes aegypti |
|
29
|
101
|
3ui4A |
0.8 a resolution crystal structure of human parvulin 14 |
|
29
|
101
|
3ui5A |
Crystal structure of human parvulin 14 |
|
49
|
173
|
3uchA |
Crystal structure of a peptidyl-prolyl cis-trans isomerase e (ppie) from homo sapiens at 2.50 a resolution |
|
30
|
101
|
3ui6A |
0.89 a resolution crystal structure of human parvulin 14 in complex with oxidized dtt |
|
45
|
158
|
3tczA |
Human pin1 bound to cis peptidomimetic inhibitor |
|
47
|
157
|
3tc5A |
Selective targeting of disease-relevant protein binding domains by o-phosphorylated natural product derivatives |
|
47
|
158
|
3tdbA |
Human pin1 bound to trans peptidomimetic inhibitor |
|
40
|
163
|
3t1uA |
Crystal structure of the complex of cyclophilin-a enzyme from azotobacter vinelandii with sucafpfpna peptide |
|
46
|
166
|
3s6mA |
The structure of a peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei |
|
55
|
172
|
5ybaA |
Dimeric cyclophilin from t.vaginalis in complex with myb1 peptide |
|
46
|
164
|
3rcgA |
Human cyclophilin d complexed with dimethylformamide |
|
56
|
164
|
3rckX |
Human cyclophilin d complexed with a fragment |
|
52
|
164
|
3rdbA |
Human cyclophilin d complexed with a fragment |
|
77
|
252
|
3rfwA |
The virulence factor peb4 and the periplasmic protein cj1289 are two structurally-related sura-like chaperones in the human pathogen campylobacter jejuni |
|
53
|
164
|
3rddA |
Human cyclophilin a complexed with an inhibitor |
|
57
|
164
|
3rciX |
Human cyclophilin d complexed with 5-methyl-1,2-oxazol-3-amine |
|
56
|
164
|
3rdaX |
Human cyclophilin d complexed with a fragment |
|
53
|
164
|
3rd9X |
Human cyclophilin d complexed with a fragment |
|
51
|
164
|
3rdcA |
Human cyclophilin d complexed with an inhibitor |
|
73
|
356
|
3rfyA |
Crystal structure of arabidopsis thaliana cyclophilin 38 (atcyp38) |
|
55
|
164
|
3rcfA |
Human cyclophilin d complexed with n-[(4-aminophenyl)sulfonyl]benzamide |
|
55
|
164
|
3rclA |
Human cyclophilin d complexed with a fragment |
|
16
|
153
|
6h3jB |
Structural snapshots of the type 9 protein translocon plug-complex |
|
16
|
155
|
5mqfV |
Cryo-em structure of a human spliceosome activated for step 2 of splicing (c* complex) |
|
24
|
178
|
2mc9A |
Cat r 1 |
|
56
|
165
|
5wc7A |
Cypa mutant - i97v s99t c115s |
|
3
|
33
|
5vtkA |
Structure of pin1 ww domain variant 1 with beta3-ser loop substitution |
|
3
|
31
|
5vtiA |
Structure of pin1 ww domain sequence 3 with [r,r]-acpc loop substitution |
|
5
|
33
|
5vtjA |
Structure of pin1 ww domain sequence 1 substituted with [s,s]acpc |
|
47
|
191
|
5v8tA |
Crystal structure of smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed with sf354 |
|
42
|
158
|
5uy9A |
Prolyl isomerase pin1 r14a mutant bound with brd4 peptide |
|
84
|
273
|
5tvlA |
Crystal structure of foldase protein prsa from streptococcus pneumoniae str. canada mdr_19a |
|
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 |
|
51
|
163
|
5t9zA |
Discovery of a potent cyclophilin inhibitor (compound 6) 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 |
|
116
|
432
|
5owjA |
The dynamic dimer structure of the chaperone trigger factor (conformer 2) |
|
128
|
412
|
5ompA |
Human fkbp5 protein |
|
112
|
432
|
5owiA |
The dynamic dimer structure of the chaperone trigger factor (conformer 1) |
|
34
|
128
|
5obkA |
The fk1 domain of fkbp51 in complex with (1s,5s,6r)-10-((3,5-dichlorophenyl)sulfonyl)-5-(hydroxymethyl)-3-(pyridin-2-ylmethyl)-3,10-diazabicyclo[4.3.1]decan-2-one |
|
56
|
164
|
5nwoA |
Human cyclophilin d complexed with inhibitor |
