|
66
|
210
|
1q6iA |
Crystal structure of a truncated form of fkpa from escherichia coli, in complex with immunosuppressant fk506 |
|
42
|
158
|
1pinA |
Pin1 peptidyl-prolyl cis-trans isomerase from homo sapiens |
|
69
|
210
|
1q6hA |
Crystal structure of a truncated form of fkpa from escherichia coli |
|
73
|
213
|
1q6uA |
Crystal structure of fkpa from escherichia coli |
|
58
|
237
|
1q1cA |
Crystal structure of n(1-260) of human fkbp52 |
|
99
|
283
|
1p5qA |
Crystal structure of fkbp52 c-terminal domain |
|
32
|
117
|
1p9yA |
Ribosome binding of e. coli trigger factor mutant f44l. |
|
23
|
116
|
1pbkA |
Homologous domain of human fkbp25 |
|
29
|
115
|
1omsA |
Structure determination by mad: e.coli trigger factor binding at the ribosomal exit tunnel. |
|
46
|
165
|
1ocaA |
Human cyclophilin a, unligated, nmr, 20 structures |
|
26
|
107
|
1nsgA |
The structure of the immunophilin-immunosuppressant fkbp12-rapamycin complex interacting with human frap |
|
48
|
165
|
1nmkA |
The sanglifehrin-cyclophilin interaction: degradation work, synthetic macrocyclic analogues, x-ray crystal structure and binding data |
|
27
|
114
|
1nmwA |
Solution structure of the ppiase domain of human pin1 |
|
30
|
163
|
1nmvA |
Solution structure of human pin1 |
|
50
|
165
|
1mikA |
The role of water molecules in the structure-based design of (5-hydroxynorvaline)-2-cyclosporin: synthesis, biological activity, and crystallographic analysis with cyclophilin a |
|
52
|
173
|
1mzwA |
Crystal structure of a u4/u6 snrnp complex between human spliceosomal cyclophilin h and a u4/u6-60k peptide |
|
26
|
125
|
1n1aA |
Crystal structure of the n-terminal domain of human fkbp52 |
|
54
|
165
|
1m9xA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) m-type h87a,a88m,g89a complex. |
|
54
|
165
|
1m9yA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) m-type h87a,g89a complex. |
|
53
|
164
|
1m9eA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) m-type h87a complex. |
|
50
|
165
|
1m9fA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) m-type h87a,a88m complex. |
|
44
|
164
|
1lopA |
Cyclophilin a complexed with succinyl-ala-pro-ala-p-nitroanilide |
|
122
|
403
|
1m5yA |
Crystallographic structure of sura, a molecular chaperone that facilitates outer membrane porin folding |
|
49
|
164
|
1mf8C |
Crystal structure of human calcineurin complexed with cyclosporin a and human cyclophilin |
|
55
|
165
|
1m9cA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) m-type complex. |
|
52
|
165
|
1m9dA |
X-ray crystal structure of cyclophilin a/hiv-1 ca n-terminal domain (1-146) o-type chimera complex. |
|
47
|
165
|
1m63C |
Crystal structure of calcineurin-cyclophilin-cyclosporin shows common but distinct recognition of immunophilin-drug complexes |
|
110
|
380
|
1kt0A |
Structure of the large fkbp-like protein, fkbp51, involved in steroid receptor complexes |
|
108
|
394
|
1kt1A |
Structure of the large fkbp-like protein, fkbp51, involved in steroid receptor complexes |
|
50
|
160
|
1jvwA |
Trypanosoma cruzi macrophage infectivity potentiator (tcmip) |
|
130
|
364
|
1ihgA |
Bovine cyclophilin 40, monoclinic form |
|
52
|
182
|
1h0pA |
Cyclophilin_5 from c. elegans |
|
16
|
92
|
1jntA |
Nmr structure of the e. coli peptidyl-prolyl cis/trans-isomerase parvulin 10 |
|
27
|
107
|
1fkhA |
Design, synthesis, and kinetic evaluation of high-affinity fkbp ligands, and the x-ray crystal structures of their complexes with fkbp12 |
|
27
|
107
|
1eymA |
Fk506 binding protein mutant, homodimeric complex |
|
25
|
107
|
1fapA |
The structure of the immunophilin-immunosuppressant fkbp12-rapamycin complex interacting with human frap |
|
25
|
107
|
1fkkA |
Atomic structure of fkbp12, an immunophilin binding protein |
|
27
|
107
|
1fklA |
Atomic structure of fkbp12-rapaymycin, an immunophilin-immunosuppressant complex |
|
26
|
107
|
1fkfA |
Atomic structure of fkbp-fk506, an immunophilin-immunosuppressant complex |
|
40
|
167
|
1f8aB |
Structural basis for the phosphoserine-proline recognition by group iv ww domains |
|
25
|
107
|
1fkdA |
Fk-506 binding protein: three-dimensional structure of the complex with the antagonist l-685,818 |
|
64
|
204
|
1fd9A |
Crystal structure of the macrophage infectivity potentiator protein (mip) a major virulence factor from legionella pneumophila |
|
12
|
107
|
1fksA |
Solution structure of fkbp, a rotamase enzyme and receptor for fk506 and rapamycin |
|
26
|
107
|
1fkgA |
Design, synthesis, and kinetic evaluation of high-affinity fkbp ligands, and the x-ray crystal structures of their complexes with fkbp12 |
|
25
|
107
|
1fkiA |
Design, synthesis, and kinetic evaluation of high-affinity fkbp ligands, and the x-ray crystal structures of their complexes with fkbp12 |
|
26
|
107
|
1fkbA |
Atomic structure of the rapamycin human immunophilin fkbp-12 complex |
|
26
|
107
|
1fkjA |
Atomic structure of fkbp12-fk506, an immunophilin immunosuppressant complex |
|
48
|
165
|
1fglA |
Cyclophilin a complexed with a fragment of hiv-1 gag protein |
|
19
|
107
|
1fktA |
Solution structure of fkbp, a rotamase enzyme and receptor for fk506 and rapamycin |
|
53
|
172
|
1e8kA |
Cyclophilin 3 complexed with dipeptide ala-pro |
