|
52
|
165
|
5noxA |
Structure of cyclophilin a in complex with 2-chloropyridin-3-amine |
|
49
|
165
|
5novA |
Structure of cyclophilin a in complex with hexahydropyrimidine-2-thione |
|
50
|
165
|
5nozA |
Structure of cyclophilin a in complex with 3,4-diaminobenzohydrazide |
|
52
|
165
|
5noyA |
Structure of cyclophilin a in complex with 3,4-diaminobenzamide |
|
52
|
165
|
5nosA |
Structure of cyclophilin a in complex with 3-amino-1h-pyridin-2-one |
|
52
|
165
|
5noqA |
Structure of cyclophilin a in complex with 3-chloropyridin-2-amine |
|
53
|
165
|
5notA |
Structure of cyclophilin a in complex with 4-chloropyrimidin-5-amine |
|
53
|
165
|
5nowA |
Structure of cyclophilin a in complex with pyridine-3,4-diamine |
|
53
|
165
|
5norA |
Structure of cyclophilin a in complex with 3-methylpyridin-2-amine |
|
124
|
413
|
5njxA |
Human fkbp51 protein in complex with c-terminal peptide of human hsp 90-alpha |
|
54
|
165
|
5nouA |
Structure of cyclophilin a in complex with hexahydropyrimidin-2-one |
|
54
|
164
|
5kv4A |
Human cyclophilin a at 278k, data set 6 |
|
55
|
164
|
5kusA |
Human cyclophilin a at 100k, data set 6 |
|
56
|
164
|
5kv6A |
Human cyclophilin a at 278k, data set 8 |
|
57
|
164
|
5kv2A |
Human cyclophilin a at 278k, data set 4 |
|
36
|
155
|
5i7pA |
Crystal structure of fkbp12-if(slyd), a chimeric protein of human fkbp12 and the insert in flap domain of ecoli slyd |
|
126
|
380
|
5b3wA |
Crystal structure of hpin1 ww domain (5-15) fused with maltose-binding protein in c2221 form |
|
57
|
165
|
5a0eA |
Crystal structure of cyclophilin d in complex with csa analogue, jw47. |
|
24
|
115
|
5ht1A |
Structure of apo c. glabrata fkbp12 |
|
31
|
117
|
5gphA |
Solution structure of the pin1-ppiase (s138a) mutant |
|
25
|
117
|
5gpgA |
Co-crystal structure of the fk506 binding domain of human fkbp25, rapamycin and the frb domain of human mtor |
|
46
|
164
|
5fjbC |
Cyclophilin a stabilize hiv-1 capsid through a novel non- canonical binding site |
|
53
|
164
|
5f66A |
High-resolution isotropic multiconformer synchrotron model of cypa at 273 k |
|
52
|
164
|
4zscA |
Human cyclophilin d complexed with an inhibitor at room temperature |
|
76
|
267
|
5ex2A |
Crystal structure of cyclophilin aquacyp293 from hirschia baltica |
|
53
|
164
|
4zsdA |
Human cyclophilin d complexed with an inhibitor at room temperature |
|
84
|
243
|
5ez1A |
Crystal structure of cell binding factor 2 from helicobacter pylori in complex with i2ca |
|
32
|
128
|
5diuA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand 2-(3-((r)-1-((s)-1-((s)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamido)-3-(3,4-dimethoxyphenyl)propyl)phenoxy)acetic acid |
|
31
|
128
|
5ditA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand (1r)-3-(3,4-dimethoxyphenyl)-1-f3-[2-(morpholin-4-yl)ethoxy]phenylgpropyl(2s)-1-[(2s,3r)-2-cyclohexyl-3-hydroxybutanoyl]piperidine-2-carboxylate |
|
27
|
120
|
5d75A |
Crystal structure of human fkbd25 in complex with fk506 |
|
33
|
127
|
5divA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand (s)-n-(1-carbamoylcyclopentyl)-1-((s)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamide |
|
53
|
163
|
4yulA |
Multiconformer synchrotron model of cypa at 280 k |
|
50
|
163
|
4yujA |
Multiconformer synchrotron model of cypa at 240 k |
|
53
|
164
|
4xncA |
Crystal structure at room temperature of cyclophilin d in complex with an inhibitor |
|
16
|
115
|
4urdA |
Cryo-em map of trigger factor bound to a translating ribosome |
|
75
|
257
|
4wo7A |
Crystal structure of prsa from bacillus subtilis |
|
29
|
121
|
4w9pA |
The fk1 domain of fkbp51 in complex with (1s,5s,6r)-10-[(3,5-dichlorophenyl)sulfonyl]-5-[(1s)-1,2-dihydroxyethyl]-3-[2-(3,4-dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one |
|
32
|
128
|
4w9qA |
The fk1 domain of fkbp51 in complex with (1s,5s,6r)-10-[(3,5-dichlorophenyl)sulfonyl]-3-[2-(3,4-dimethoxyphenoxy)ethyl]-5-ethyl-3,10-diazabicyclo[4.3.1]decan-2-one |
|
31
|
123
|
4w9oA |
The fk1 domain of fkbp51 in complex with (1s,5s,6r)-10-[(3,5-dichlorophenyl)sulfonyl]-5-[(1r)-1,2-dihydroxyethyl]-3-[2-(3,4-dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one |
|
35
|
128
|
4tw6A |
The fk1 domain of fkbp51 in complex with ifit1 |
|
36
|
128
|
4tx0A |
The fk1 domain of fkbp51 in complex with (1s,5s,6r)-10-[(3,5-dichlorophenyl)sulfonyl]-5-(2-methoxyethoxy)-3-(2-methoxyethyl)-3,10-diazabicyclo[4.3.1]decan-2-one |
|
45
|
113
|
4tnsA |
Structure of pin1 ppiase domain bound with all-trans retinoic acid |
|
45
|
157
|
4u84A |
Human pin1 with s-hydroxyl-cysteine 113 |
|
47
|
166
|
4s1eA |
Crystal structure of cyclophilin mutant l120a from leishmania donovani at 2.22 angstrom. |
|
44
|
158
|
4u86A |
Human pin1 with cysteine sulfonic acid 113 |
|
53
|
235
|
4tw8A |
The fk1-fk2 domains of fkbp52 in complex with ifit-fl |
|
46
|
157
|
4u85A |
Human pin1 with cysteine sulfinic acid 113 |
|
46
|
166
|
4s1jA |
Crystal structure of cyclophilin mutant v33a from leishmania donovani at 2.3 angstrom. |
|
38
|
113
|
4tyoA |
Ppiase in complex with a non-phosphate small molecule inhibitor. |
|
29
|
128
|
4tw7A |
The fk1 domain of fkbp51 in complex with ifit4 |
