|
7
|
23
|
7lwhB |
Human neurofibromin 2/merlin residues 1-339 in complex with lats1 |
|
102
|
248
|
7k03A |
Crystal structure of the tandem bromodomain (bd1 and bd2) of human taf1 bound to atr kinase inhibitor azd6738 |
|
101
|
250
|
7k0dA |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to mtorc1/2 inhibitor azd3147 |
|
52
|
130
|
7k1pA |
Crystal structure of the second bromodomain (bd2) of human taf1 bound to bromosporine |
|
55
|
137
|
7jjgA |
Crystal structure of the second bromodomain (bd2) of human taf1 bound to atr kinase inhibitor az20 |
|
54
|
128
|
7k0uA |
Crystal structure of the second bromodomain (bd2) of human taf1 bound to plk1 kinase inhibitor bi2536 |
|
98
|
247
|
7k27A |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to atr inhibitor az20 |
|
58
|
135
|
7jtcA |
Crystal structure of the second bromodomain (bd2) of human taf1 bound to zs1-322 |
|
55
|
137
|
7jspA |
Crystal structure of the second bromodomain (bd2) of human taf1 bound to atr kinase inhibitor azd6738 |
|
72
|
273
|
7f3gA |
Crystal structure of dclk1 kinase domain in complex with ruxolitinib |
|
504
|
1544
|
7ni4A |
Human atm kinase domain with bound m4076 inhibitor |
|
72
|
290
|
7cp3A |
Crystal structure of pak4 in complex with inhibitor 47 |
|
91
|
292
|
7cp4A |
Crystal structure of pak4 in complex with inhibitor 55 |
|
140
|
406
|
7bmkA |
Atp-competitive partial antagonists-'pair's-rheostatically modulate ire1alpha's kinase helix-alphac to segregate its rnase-mediated biological outputs |
|
113
|
328
|
7atvA |
Structure of protein kinase ck2 catalytic subunit (csnk2a2 gene product) in complex with the bivalent inhibitor kn2 |
|
108
|
430
|
7apjA |
Structure of autoinhibited akt1 reveals mechanism of pip3-mediated activation |
|
111
|
328
|
7at9A |
Structure of protein kinase ck2 catalytic subunit (csnk2a2 gene product) in complex with the atp-competitive inhibitor mb002 and the alphad-pocket ligand 3,4-dichlorophenethylamine |
|
117
|
332
|
7at5A |
Structure of protein kinase ck2 catalytic subunit (csnk2a1 gene product) in complex with the bivalent inhibitor kn2 |
|
53
|
299
|
7a0jAAA |
Crystal structure of the crinkly wd40 ectodomain from the arabidopsis thaliana receptor kinase acr4 |
|
65
|
355
|
6zueB |
Crystal structure of human ddb1 bound to human dcaf1 (amino acid residues 1046-1396) |
|
171
|
482
|
7s67A |
Extended conformation of daytime state kaic |
|
167
|
485
|
7s66A |
Extended conformation of nighttime state kaic |
|
160
|
460
|
7s65A |
Compressed conformation of nighttime state kaic |
|
606
|
2555
|
7pe8A |
Cryo-em structure of deptor bound to human mtor complex 2, focussed on one protomer |
|
615
|
2555
|
7pe9A |
Cryo-em structure of deptor bound to human mtor complex 2, dept-bound subset local refinement |
|
615
|
2555
|
7pe7A |
Cryo-em structure of deptor bound to human mtor complex 2, overall refinement |
|
80
|
306
|
7ooxA |
Crystal structure of pim1 in complex with arc-3126 |
|
92
|
316
|
7p1lA |
The mark3 kinase domain bound to aa-cs-1-008 |
|
115
|
328
|
7opsA |
Crystal structure of haspin in complex with zw282 (compound 2a) |
|
98
|
248
|
7lb0A |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to zs1-295 |
|
99
|
247
|
7lb2A |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to zs1-589 |
|
100
|
249
|
7lb1A |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to zs1-585 |
|
88
|
291
|
7cmbA |
Crystal structure of pak4 in complex with inhibitor 41 |
|
80
|
268
|
7bjdA |
Crystal structure of chk1-10pt-mutant complex with compound 3 |
|
81
|
268
|
7bjhA |
Crystal structure of chk1-10pt-mutant complex with compound 8 |
|
78
|
267
|
7bjeA |
Crystal structure of chk1-10pt-mutant complex with adenine |
|
76
|
266
|
7bjrA |
Crystal structure of chk1-10pt-mutant complex with compound 18 |
|
72
|
263
|
7bjxA |
Crystal structure of chk1-10pt-mutant complex with compound 26 |
|
73
|
265
|
7bknA |
Crystal structure of chk1 complex with adenine |
|
84
|
267
|
7bk3A |
Crystal structure of chk1-10pt-mutant complex with compound 45 |
|
83
|
267
|
7bk2A |
Crystal structure of chk1-10pt-mutant complex with compound 44 |
|
78
|
265
|
7bkoA |
Crystal structure of chk1 complex with compound 9 |
|
77
|
264
|
7bk1A |
Crystal structure of chk1-10pt-mutant complex with compound 32 |
|
81
|
266
|
7bjmA |
Crystal structure of chk1-10pt-mutant complex with compound 10 |
|
83
|
268
|
7bjjA |
Crystal structure of chk1-10pt-mutant complex with compound 9 |
|
74
|
267
|
7bjoA |
Crystal structure of chk1-10pt-mutant complex with compound 13 |
|
101
|
256
|
7l6xA |
Crystal structure of the tandem bromodomain (bd1, bd2) of human taf1 bound to gne-371 |
|
365
|
1988
|
7lhwA |
Structure of the lrrk2 monomer |
|
354
|
1970
|
7li3A |
Structure of the lrrk2 g2019s mutant |
|
345
|
1970
|
7li4A |
Structure of lrrk2 after symmetry expansion |
