|
43
|
173
|
4r3eA |
Structure of the spliceosomal peptidyl-prolyl cis-trans isomerase cwc27 from homo sapiens |
|
30
|
122
|
4r0xA |
Allosteric coupling of conformational transitions in the fk1 domain of fkbp51 near the site of steroid receptor interaction |
|
52
|
196
|
4r3fA |
Structure of the spliceosomal peptidyl-prolyl cis-trans isomerase cwc27 from chaetomium thermophilum |
|
31
|
125
|
4qt3A |
Crystal structure resolution of plasmodium falciparum fk506 binding domain (fkbp35) in complex with rapamycin at 1.4a resolution |
|
39
|
157
|
4qibA |
Oxidation-mediated inhibition of the peptidyl-prolyl isomerase pin1 |
|
34
|
122
|
4qt2A |
Crystal structure of the fk506-binding domain of plasmodium falciparum fkbp35 in complex with rapamycin |
|
94
|
270
|
4qccA |
Structure of a cube-shaped, highly porous protein cage designed by fusing symmetric oligomeric domains |
|
33
|
150
|
4odmA |
Structure of slyd from thermus thermophilus in complex with s2-w23a peptide |
|
24
|
104
|
4odrA |
Structure of slyd delta-if from thermus thermophilus in complex with fk506 |
|
27
|
107
|
4n19A |
Structural basis of conformational transitions in the active site and 80 s loop in the fk506 binding protein fkbp12 |
|
55
|
164
|
4o8hA |
0.85a resolution structure of peg 400 bound cyclophilin d |
|
35
|
150
|
4odoA |
Structure of slyd from thermus thermophilus in complex with fk506 |
|
18
|
102
|
4nnrA |
Fkbp13-fk506 complex |
|
54
|
164
|
4o8iA |
1.45a resolution structure of peg 400 bound cyclophilin d |
|
52
|
165
|
4n1oA |
Structure of cyclophilin a in complex with saccharin. |
|
24
|
110
|
4odqA |
Structure of slyd delta-if from thermus thermophilus in complex with s3 peptide |
|
116
|
301
|
4ny3A |
Human ptpa in complex with peptide |
|
50
|
165
|
4n1rA |
Structure of cyclophilin a in complex with benzenesulfonohydrazide. |
|
32
|
150
|
4odnA |
Structure of slyd from thermus thermophilus in complex with s2-plus peptide |
|
49
|
165
|
4n1nA |
Structure of cyclophilin a in complex with benzamide. |
|
23
|
110
|
4odpA |
Structure of slyd delta-if from thermus thermophilus in complex with s2-w23a peptide |
|
31
|
150
|
4odlA |
Structure of slyd from thermus thermophilus in complex with s2 peptide |
|
51
|
165
|
4n1sA |
Structure of cyclophilin a in complex with benzohydrazide. |
|
52
|
165
|
4n1qA |
Structure of cyclophilin a in complex with cyclohexanecarboxamide. |
|
50
|
168
|
4n1mA |
Structure of cyclophilin a in complex with glypro. |
|
51
|
165
|
4n1pA |
Structure of cyclophilin a in complex with picolinamide. |
|
52
|
189
|
4mspA |
Crystal structure of human peptidyl-prolyl cis-trans isomerase fkbp22 (aka fkbp14) containing two ef-hand motifs |
|
32
|
122
|
4mgvA |
Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with inhibitor d5 |
|
59
|
234
|
4layA |
Crystal structure analysis of fkbp52, complex with i63 |
|
29
|
124
|
4l6eA |
Crystal structure of the ranbd1 fourth domain of e3 sumo-protein ligase ranbp2. northeast structural genomics consortium (nesg) target hr9193b |
|
56
|
235
|
4lawA |
Crystal structure analysis of fkbp52, crystal form iii |
|
56
|
237
|
4laxA |
Crystal structure analysis of fkbp52, complex with fk506 |
|
107
|
301
|
4lacB |
Crystal structure of protein phosphatase 2a (pp2a) and pp2a phosphatase activator (ptpa) complex with atpgammas |
|
58
|
240
|
4lavA |
Crystal structure analysis of fkbp52, crystal form ii |
|
55
|
170
|
4jcpA |
Structure of cyclophilin b from brugia malayi |
|
53
|
170
|
4hy7A |
Structural and biochemical characterization of a cytosolic wheat cyclophilin tacypa-1 |
|
35
|
127
|
4jfiA |
Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with compound 1-[(9s,13r,13ar)-1,3-dimethoxy-8-oxo-5,8,9,10,11,12,13,13a-octahydro-6h-9,13-epiminoazocino[2,1-a]isoquinolin-14-yl]-2-(3,4,5-trimethoxyphenyl)ethane-1,2-dione |
|
50
|
164
|
4j5eX |
Human cyclophilin d complexed with an inhibitor |
|
34
|
128
|
4jfmA |
Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with 2-(3,4-dimethoxyphenoxy)ethyl (2s)-1-[(2-oxo-2,3-dihydro-1,3-benzothiazol-6-yl)sulfonyl]piperidine-2-carboxylate |
|
34
|
122
|
4j4oA |
Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with d44 |
|
34
|
128
|
4jfkA |
Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with (1s,6r)-3-[2-(3,4-dimethoxyphenoxy)ethyl]-10-[(2-oxo-2,3-dihydro-1,3-benzothiazol-6-yl)sulfonyl]-3,10-diazabicyclo[4.3.1]decan-2-one |
|
57
|
164
|
4j5aX |
Human cyclophilin d complexed with an inhibitor |
|
21
|
107
|
4iq2A |
P21 crystal form of fkbp12.6 |
|
34
|
128
|
4jfjA |
Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with compound (1s,6r)-10-(1,3-benzothiazol-6-ylsulfonyl)-3-[2-(3,4-dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one |
|
34
|
128
|
4jflA |
Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with 6-({(1s,5r)-3-[2-(3,4-dimethoxyphenoxy)ethyl]-2-oxo-3,9-diazabicyclo[3.3.1]non-9-yl}sulfonyl)-1,3-benzothiazol-2(3h)-one |
|
53
|
164
|
4j5bA |
Human cyclophilin d complexed with an inhibitor |
|
33
|
121
|
4itzA |
Crystal structure of the fk506 binding domain of plasmodium vivax fkbp35 in complex with a tetrapeptide substrate |
|
52
|
164
|
4j59A |
Human cyclophilin d complexed with an inhibitor |
|
53
|
164
|
4ipzA |
Smbz bound to cyclophilin a |
|
55
|
164
|
4j58A |
Human cyclophilin d complexed with an inhibitor |
