122
|
344
|
4mnmA |
Crystal structure of gh18 chitinase (g77w/e119q mutant) from cycas revoluta in complex with (glcnac)4 |
120
|
361
|
4mpkA |
Crystal structure of the complex of buffalo signaling protein spb-40 with n-acetylglucosamine at 2.65 a resolution |
32
|
122
|
4mgvA |
Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with inhibitor d5 |
122
|
344
|
4mnkA |
Crystal structure of gh18 chitinase from cycas revoluta in complex with (glcnac)3 |
121
|
344
|
4mnlA |
Crystal structure of gh18 chitinase (g77w/e119q mutant) from cycas revoluta in complex with (glcnac)4 |
121
|
361
|
4mavA |
Crystal structure of signaling protein spb-40 complexed with 5-hydroxymethyl oxalanetriol at 2.80 a resolution |
128
|
398
|
4lgxA |
Structure of chitinase d from serratia proteamaculans revealed an unusually constrained substrate binding site |
51
|
208
|
4kqzA |
Structure of the receptor binding domain (rbd) of mers-cov spike |
59
|
234
|
4layA |
Crystal structure analysis of fkbp52, complex with i63 |
56
|
235
|
4lawA |
Crystal structure analysis of fkbp52, crystal form iii |
56
|
237
|
4laxA |
Crystal structure analysis of fkbp52, complex with fk506 |
44
|
208
|
4kr0B |
Complex structure of mers-cov spike rbd bound to cd26 |
46
|
204
|
4l72B |
Crystal structure of mers-cov complexed with human dpp4 |
58
|
240
|
4lavA |
Crystal structure analysis of fkbp52, crystal form ii |
56
|
209
|
4l3nA |
Crystal structure of the receptor-binding domain from newly emerged middle east respiratory syndrome coronavirus |
30
|
132
|
4jysA |
Crystal structure of fkbp25 from plasmodium vivax |
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 |
20
|
117
|
4it6A |
Crystal structure of amino acid residues 1-120 of cg17282 |
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 |
21
|
107
|
4iq2A |
P21 crystal form of fkbp12.6 |
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 |
34
|
122
|
4j4oA |
Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with d44 |
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 |
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 |
33
|
121
|
4itzA |
Crystal structure of the fk506 binding domain of plasmodium vivax fkbp35 in complex with a tetrapeptide substrate |
25
|
107
|
4iqcA |
P3121 crystal form of fkbp12.6 |
59
|
210
|
4it4A |
Crystal structure of residues 1-211 of cg17282 |
28
|
123
|
4j4nA |
Crystal structure of fk506 binding domain of plasmodium falciparum fkbp35 in complex with d44 |
28
|
107
|
4ipxA |
Analyzing the visible conformational substates of the fk506 binding protein fkbp12 |
12
|
98
|
4harA |
Crystal structure of rubella virus capsid protein (residues 127-277) |
14
|
98
|
4hbeA |
Crystal structure of rubella virus capsid protein (residues 127-277) |
8
|
96
|
4hboA |
Crystal structure of rubella virus capsid protein (residues 127-277) |
48
|
191
|
4ggqA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed with cj40 |
46
|
191
|
4g50A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj168 |
48
|
192
|
4givA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj183 |
29
|
108
|
4g2pA |
Crystal structure of peptidyl-prolyl cis-trans isomerase domain ii of molecular chaperone sura from salmonella enterica subsp. enterica serovar typhimurium str. 14028s |
44
|
190
|
4fn2A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj37 |
124
|
394
|
3qokA |
Crystal structure of putative chitinase ii from klebsiella pneumoniae |
30
|
124
|
3pa7A |
Crystal structure of fkbp from plasmodium vivax in complex with tetrapeptide alpf |
53
|
223
|
3prbA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
38
|
150
|
3pr9A |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
33
|
150
|
3praA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
36
|
223
|
3prdA |
Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26 |
187
|
515
|
3oa5A |
The structure of chi1, a chitinase from yersinia entomophaga |
49
|
158
|
3oobA |
Structural and functional insights of directly targeting pin1 by epigallocatechin-3-gallate |
42
|
157
|
3odkA |
Discovery of cell-active phenyl-imidazole pin1 inhibitors by structure-guided fragment evolution |
34
|
125
|
3o5fA |
Fk1 domain of fkbp51, crystal form vii |
33
|
128
|
3o5rA |
Complex of fk506 with the fk1 domain mutant a19t of fkbp51 |
31
|
124
|
3o5jA |
Fk1 domain of fkbp51, crystal form iii |
35
|
127
|
3o5mA |
Fk1 domain mutant a19t of fkbp51, crystal form ii |