|
13
|
107
|
5t9rA |
Structure of rabbit ryr1 (ca2+-only dataset, class 3) |
|
12
|
107
|
5tazA |
Structure of rabbit ryr1 (ryanodine dataset, class 3) |
|
12
|
107
|
5tasA |
Structure of rabbit ryr1 (caffeine/atp/egta dataset, class 1) |
|
12
|
107
|
5tatA |
Structure of rabbit ryr1 (caffeine/atp/egta dataset, class 2) |
|
9
|
107
|
5tayA |
Structure of rabbit ryr1 (ryanodine dataset, class 2) |
|
54
|
164
|
5ccsX |
Human cyclophilin d complexed with inhibitor |
|
54
|
164
|
5ccnA |
Human cyclophilin d complexed with inhibitor |
|
51
|
164
|
5cyhA |
Cyclophilin a complexed with dipeptide gly-pro |
|
53
|
164
|
5ccrA |
Human cyclophilin d complexed with inhibitor |
|
54
|
164
|
5cbvA |
Human cyclophilin d complexed with inhibitor |
|
56
|
164
|
5cbuA |
Human cyclophilin d complexed with inhibitor. |
|
56
|
164
|
5cbtA |
Human cyclophilin d complexed with inhibitor |
|
54
|
164
|
5cbwA |
Human cyclophilin d complexed with inhibitor. |
|
54
|
164
|
5ccqA |
Human cyclophilin d complexed with inhibitor |
|
32
|
127
|
5bxjA |
Complex of the fk1 domain mutant a19t of fkbp51 with 4-nitrophenol |
|
122
|
387
|
5bmyA |
Crystal structure of hpin1 ww domain (5-21) fused with maltose-binding protein |
|
126
|
402
|
5b3zA |
Crystal structure of hpin1 ww domain (5-39) fused with maltose-binding protein |
|
122
|
382
|
5b3yA |
Crystal structure of hpin1 ww domain (5-23) fused with maltose-binding protein |
|
108
|
377
|
5b3xA |
Crystal structure of hpin1 ww domain (5-15) fused with maltose-binding protein in p41212 form |
|
50
|
164
|
4yuiA |
Multiconformer synchrotron model of cypa at 180 k |
|
48
|
163
|
4yukA |
Multiconformer synchrotron model of cypa at 260 k |
|
52
|
164
|
4yuhA |
Multiconformer synchrotron model of cypa at 150 k |
|
51
|
163
|
4yunA |
Multiconformer synchrotron model of cypa at 310 k |
|
50
|
163
|
4yuoA |
High-resolution multiconformer synchrotron model of cypa at 273 k |
|
52
|
165
|
4yugA |
Multiconformer synchrotron model of cypa at 100 k |
|
52
|
163
|
4yumA |
Multiconformer synchrotron model of cypa at 300 k |
|
49
|
164
|
4yupA |
Multiconformer fixed-target x-ray free electron (xfel) model of cypa at 273 k |
|
52
|
164
|
4totA |
Crystal structure of rat cyclophilin d in complex with a potent nonimmunosuppressive inhibitor |
|
51
|
162
|
4eyvA |
Crystal structure of cyclophilin a like protein from piriformospora indica |
|
26
|
107
|
4fapA |
Atomic structures of the rapamycin analogs in complex with both human fkbp12 and frb domain of frap |
|
54
|
170
|
4e1qA |
Crystal structure of wheat cyclophilin a at 1.25 a resolution |
|
30
|
132
|
4drhA |
Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor at low ph |
|
29
|
113
|
4dz3A |
Crystal structure of a peptidyl-prolyl cis-trans isomerase with surface mutation m61h from burkholderia pseudomallei complexed with fk506 |
|
27
|
121
|
4drjA |
O-crystal structure of the ppiase domain of fkbp52, rapamycin and the frb fragment of mtor |
|
25
|
113
|
4dz2A |
Crystal structure of a peptidyl-prolyl cis-trans isomerase with surface mutation r92g from burkholderia pseudomallei complexed with fk506 |
|
34
|
128
|
4drmA |
Evaluation of synthetic fk506 analogs as ligands for fkbp51 and fkbp52: complex of fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1-({[(2s)-1-{[(1s,2r)-2-ethyl-1-hydroxycyclohexyl](oxo)acetyl}piperidin-2-yl]carbonyl}oxy)propyl]phenoxy}acetic acid |
|
36
|
128
|
4drpA |
Evaluation of synthetic fk506 analogs as ligands for the fk506-binding proteins 51 and 52: complex of fkbp51 with 2-(3-((r)-3-(3,4-dimethoxyphenyl)-1-((s)-1-(2-((1r,2s)-2-ethyl-1-hydroxy-cyclohexyl)-2-oxoacetyl)piperidine-2-carbonyloxy)propyl)phenoxy)acetic acid from cocrystallization |
|
32
|
121
|
4driA |
Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor |
|
28
|
160
|
4dt4A |
Crystal structure of the ppiase-chaperone slpa with the chaperone binding site occupied by the linker of the purification tag |
|
36
|
128
|
4droA |
Evaluation of synthetic fk506 analogs as ligands for fkbp51 and fkbp52: complex of fkbp51 with (1r)-3-(3,4-dimethoxyphenyl)-1-phenylpropyl (2s)-1-{[(1r,2s)-2-ethyl-1-hydroxycyclohexyl](oxo)acetyl}piperidine-2-carboxylate |
|
34
|
128
|
4drkA |
Evaluation of synthetic fk506 analogs as ligands for fkbp51 and fkbp52: complex of fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1-({[(2s)-1-(3,3-dimethyl-2-oxopentanoyl)piperidin-2-yl]carbonyl}oxy)propyl]phenoxy}acetic acid |
|
39
|
128
|
4drnA |
Evaluation of synthetic fk506 analogs as ligands for fkbp51 and fkbp52: complex of fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1-({[(2s)-1-{[(1s,2r)-2-ethyl-1-hydroxycyclohexyl](oxo)acetyl}piperidin-2-yl]carbonyl}oxy)propyl]phenoxy}acetic acid |
|
35
|
128
|
4drqA |
Exploration of pipecolate sulfonamides as binders of the fk506-binding proteins 51 and 52: complex of fkbp51 with 2-(3-((r)-1-((s)-1-(3,5-dichlorophenylsulfonyl)piperidine-2-carbonyloxy)-3-(3,4-dimethoxy -phenyl)propyl)phenoxy)acetic acid |
|
49
|
164
|
4dgeA |
Trimcyp cyclophilin domain from macaca mulatta: h70c mutant, hiv-1 ca(o-loop) complex |
|
27
|
121
|
4dipA |
Crystal structure of human peptidyl-prolyl cis-trans isomerase fkbp14 |
|
47
|
163
|
4dgbA |
Trimcyp cyclophilin domain from macaca mulatta: hiv-2 ca cyclophilin-binding loop complex |
|
51
|
164
|
4cyhA |
Cyclophilin a complexed with dipeptide his-pro |
|
26
|
107
|
4dh0A |
X-ray crystal structure of 28-o-methylrapamycin complexed with fkbp12: is the cyclohexyl moiety part of the effector domain of rapamycin? |
|
45
|
163
|
4dgcA |
Trimcyp cyclophilin domain from macaca mulatta: cyclosporin a complex |
|
52
|
165
|
4dgdA |
Trimcyp cyclophilin domain from macaca mulatta: h70c mutant |
