|
17
|
120
|
1j6yA |
Solution structure of pin1at from arabidopsis thaliana |
|
17
|
151
|
1ix5A |
Solution structure of the methanococcus thermolithotrophicus fkbp |
|
14
|
96
|
1eq3A |
Nmr structure of human parvulin hpar14 |
|
8
|
85
|
1hxvA |
Ppiase domain of the mycoplasma genitalium trigger factor |
|
28
|
107
|
1f40A |
Solution structure of fkbp12 complexed with gpi-1046, a neurotrophic ligand |
|
13
|
107
|
1fkrA |
Solution structure of fkbp, a rotamase enzyme and receptor for fk506 and rapamycin |
|
8
|
106
|
1l1pA |
Solution structure of the ppiase domain from e. coli trigger factor |
|
16
|
92
|
1jnsA |
Nmr structure of the e. coli peptidyl-prolyl cis/trans-isomerase parvulin 10 |
|
12
|
104
|
1fjdA |
Human parvulin-like peptidyl prolyl cis/trans isomerase, hpar14 |
|
49
|
192
|
3uqbA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with fk506 |
|
49
|
190
|
3uqaA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation a54e from burkholderia pseudomallei complexed with fk506 |
|
101
|
317
|
5jh8A |
Crystal structure of chitinase from chromobacterium violaceum atcc 12472 |
|
27
|
111
|
5j6eA |
Structure of disulfide crosslinked a. fumigatus fkbp12(v91c) |
|
26
|
120
|
5i98A |
Structure of apo fkbp12(p104g) from c. albicans |
|
27
|
111
|
5hwbA |
Aspergillus fumigatus fkbp12 apo protein in p212121 space group |
|
25
|
120
|
5hw8A |
Candida albicans fkbp12 p104g protein bound with fk506 in c2 space group |
|
28
|
122
|
5hw7A |
Candida albicans fkbp12 apo protein in p21212 space group |
|
30
|
113
|
5hwcA |
Aspergillus fumigatus fkbp12 p90g protein bound with fk506 in p212121 space group |
|
27
|
122
|
5htgA |
Structure of apo p1 form of candida albicans fkbp12 |
|
27
|
113
|
5huaA |
Structure of c. glabrata fkbp12-fk506 complex |
|
25
|
120
|
5hw6A |
Candida albicans fkbp12 apo protein in c2 space group |
|
137
|
452
|
5hbfA |
Crystal structure of human full-length chitotriosidase (chit1) |
|
25
|
107
|
5hkgA |
Total chemical synthesis, refolding and crystallographic structure of a fully active immunophilin: calstabin 2 (fkbp12.6). |
|
32
|
127
|
5bxjA |
Complex of the fk1 domain mutant a19t of fkbp51 with 4-nitrophenol |
|
28
|
119
|
5b8iC |
Crystal structure of calcineurin a and calcineurin b in complex with fkbp12 and fk506 from coccidioides immitis rs |
|
156
|
498
|
4z2gA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 26 |
|
163
|
498
|
4z2hA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 29 |
|
162
|
498
|
4z2iA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 30 |
|
161
|
498
|
4z2jA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 31 |
|
161
|
498
|
4z2lA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 33 |
|
26
|
107
|
4fapA |
Atomic structures of the rapamycin analogs in complex with both human fkbp12 and frb domain of frap |
|
25
|
113
|
4dz2A |
Crystal structure of a peptidyl-prolyl cis-trans isomerase with surface mutation r92g from burkholderia pseudomallei complexed with fk506 |
|
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 |
|
186
|
543
|
4dwsA |
Crystal structure of a chitinase from the yersinia entomophaga toxin complex |
|
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 |
|
191
|
539
|
4dwsD |
Crystal structure of a chitinase from the yersinia entomophaga toxin complex |
|
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 |
|
184
|
539
|
4dwsC |
Crystal structure of a chitinase from the yersinia entomophaga toxin complex |
|
30
|
132
|
4drhA |
Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor at low ph |
|
190
|
540
|
4dwsB |
Crystal structure of a chitinase from the yersinia entomophaga toxin complex |
|
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 |
|
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 |
|
27
|
121
|
4dipA |
Crystal structure of human peptidyl-prolyl cis-trans isomerase fkbp14 |
|
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? |
|
24
|
108
|
4c02B |
Crystal structure of human acvr1 (alk2) in complex with fkbp12.6 and dorsomorphin |
