|
21
|
117
|
4bf8A |
Fpr4 ppi domain |
|
130
|
364
|
4ay1A |
Human ykl-39 is a pseudo-chitinase with retained chitooligosaccharide binding properties |
|
46
|
157
|
3wh0A |
Structure of pin1 complex with 18-crown-6 |
|
162
|
497
|
3wd1A |
Serratia marcescens chitinase b complexed with syn-triazole inhibitor |
|
161
|
497
|
3wd3A |
Serratia marcescens chitinase b complexed with azide inhibitor |
|
143
|
383
|
3wl1A |
Crystal structure of ostrinia furnacalis group i chitinase catalytic domain in complex with reaction products (glcnac)2,3 |
|
121
|
344
|
3wijA |
Crystal structure of a plant class v chitinase mutant from cycas revoluta in complex with (glcnac)3 |
|
143
|
383
|
3wqwA |
Crystal structure of ostrinia furnacalis group i chitinase catalytic domain in complex with a(glcn)6 |
|
139
|
383
|
3wl0A |
Crystal structure of ostrinia furnacalis group i chitinase catalytic domain e148a mutant in complex with a(glcnac)2 |
|
140
|
383
|
3wkzA |
Crystal structure of the ostrinia furnacalis group i chitinase catalytic domain e148q mutant |
|
140
|
383
|
3wqvA |
Crystal structure of ostrinia furnacalis group i chitinase catalytic domain in complex with a(glcn)5 |
|
165
|
498
|
3wd0A |
Serratia marcescens chitinase b, tetragonal form |
|
165
|
497
|
3wd2A |
Serratia marcescens chitinase b complexed with azide inhibitor |
|
165
|
497
|
3wd4A |
Serratia marcescens chitinase b complexed with azide inhibitor and quinoline compound |
|
145
|
383
|
3w4rA |
Crystal structure of an insect chitinase from the asian corn borer, ostrinia furnacalis |
|
46
|
191
|
3vawA |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation v3i from burkholderia pseudomallei complexed with fk506 |
|
26
|
108
|
3uqiA |
Crystallographic structure of fkbp12 from aedes aegypti |
|
52
|
192
|
3uf8A |
Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with a g95a surface mutation from burkholderia pseudomallei complexed with fk506 |
|
29
|
101
|
3ui5A |
Crystal structure of human parvulin 14 |
|
30
|
101
|
3ui6A |
0.89 a resolution crystal structure of human parvulin 14 in complex with oxidized dtt |
|
29
|
101
|
3ui4A |
0.8 a resolution crystal structure of human parvulin 14 |
|
45
|
158
|
3tczA |
Human pin1 bound to cis peptidomimetic inhibitor |
|
47
|
157
|
3tc5A |
Selective targeting of disease-relevant protein binding domains by o-phosphorylated natural product derivatives |
|
47
|
158
|
3tdbA |
Human pin1 bound to trans peptidomimetic inhibitor |
|
133
|
377
|
3rm8A |
Amcase in complex with compound 2 |
|
129
|
377
|
3rm9A |
Amcase in complex with compound 3 |
|
131
|
377
|
3rmeA |
Amcase in complex with compound 5 |
|
131
|
373
|
3rm4A |
Amcase in complex with compound 1 |
|
77
|
252
|
3rfwA |
The virulence factor peb4 and the periplasmic protein cj1289 are two structurally-related sura-like chaperones in the human pathogen campylobacter jejuni |
|
81
|
251
|
3rgcA |
The virulence factor peb4 and the periplasmic protein cj1289 are two structurally related sura-like chaperones in the human pathogen campylobacter jejuni |
|
164
|
498
|
4z2kA |
Serratia marcescens chitinase b complexed with macrolide inhibitor 32 |
|
24
|
115
|
5ht1A |
Structure of apo c. glabrata fkbp12 |
|
25
|
117
|
5gpgA |
Co-crystal structure of the fk506 binding domain of human fkbp25, rapamycin and the frb domain of human mtor |
|
173
|
538
|
5gqbA |
Crystal structure of chitinase-h from o. furnacalis in complex with chitohepatose |
|
166
|
536
|
5gprA |
Crystal structure of chitinase-h from ostrinia furnacalis |
|
45
|
207
|
4zs6A |
Receptor binding domain and fab complex |
|
49
|
208
|
5do2A |
Complex structure of mers-rbd bound with 4c2 antibody |
|
31
|
128
|
5ditA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand (1r)-3-(3,4-dimethoxyphenyl)-1-f3-[2-(morpholin-4-yl)ethoxy]phenylgpropyl(2s)-1-[(2s,3r)-2-cyclohexyl-3-hydroxybutanoyl]piperidine-2-carboxylate |
|
57
|
208
|
4zpwR |
Structure of unbound mers-cov spike receptor-binding domain (england1 strain). |
|
32
|
128
|
5diuA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand 2-(3-((r)-1-((s)-1-((s)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamido)-3-(3,4-dimethoxyphenyl)propyl)phenoxy)acetic acid |
|
45
|
208
|
4zpvR |
Structure of mers-coronavirus spike receptor-binding domain (england1 strain) in complex with vaccine-elicited murine neutralizing antibody d12 (crystal form 2) |
|
27
|
120
|
5d75A |
Crystal structure of human fkbd25 in complex with fk506 |
|
181
|
528
|
5dezA |
Crystal structure of acmnpv chitinase a |
|
158
|
528
|
5df0A |
Crystal structure of acmnpv chitinase a in complex with chitotrio-thiazoline dithioamide |
|
52
|
208
|
4zptR |
Structure of mers-coronavirus spike receptor-binding domain (england1 strain) in complex with vaccine-elicited murine neutralizing antibody d12 (crystal form 1) |
|
33
|
127
|
5divA |
The fk1 domain of fkbp51 in complex with the new synthetic ligand (s)-n-(1-carbamoylcyclopentyl)-1-((s)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamide |
|
137
|
369
|
4wjxA |
Crystal structure of human chitotriosidase-1 catalytic domain at 1.0 a resolution |
|
49
|
211
|
4xakA |
Crystal structure of potent neutralizing antibody m336 in complex with mers co-v rbd |
|
132
|
369
|
4wk9A |
Crystal structure of human chitotriosidase-1 catalytic domain in complex with chitobiose (0.3mm) at 1.10 a resolution |
|
133
|
369
|
4wkhA |
Crystal structure of human chitotriosidase-1 catalytic domain in complex with chitobiose (1mm) at 1.05 a resolution |
