|
112
|
326
|
5ih8A |
Melk in complex with nvs-melk1 |
|
115
|
326
|
5ihaA |
Melk in complex with nvs-melk8f |
|
109
|
326
|
5ihcA |
Melk in complex with nvs-melk12b |
|
111
|
326
|
5ih9A |
Melk in complex with nvs-melk8a |
|
93
|
293
|
5ih5A |
Human casein kinase 1 isoform delta (kinase domain) in complex with epiblastin a |
|
81
|
274
|
5iisA |
Design, synthesis and structure activity relationship of potent pan-pim kinase inhibitors derived from the pyridyl-amide scaffold |
|
96
|
293
|
5ih4A |
Human casein kinase 1 isoform delta apo (kinase domain) |
|
82
|
296
|
5imeA |
Crystal structure of p21-activated kinase 1 (pak1) in complex with compound 9 |
|
54
|
139
|
5i29A |
Taf1(2) bound to a pyrrolopyridone compound |
|
220
|
630
|
5hz1B |
Plant peptide hormone receptor rgfr1 in complex with rgf3 |
|
79
|
289
|
5i0bA |
Structure of pak4 |
|
206
|
632
|
5hz3B |
Plant peptide hormone receptor rgfr1 in complex with rgfr5 |
|
86
|
302
|
5i3rA |
Crystal structure of bmp-2-inducible kinase in complex with an indazole inhibitor |
|
56
|
135
|
5i1qA |
Second bromodomain of taf1 bound to a pyrrolopyridone compound |
|
221
|
631
|
5hz0B |
Plant peptide hormone receptor rgfr1 in complex with rgf2 |
|
72
|
311
|
5hvkA |
Crystal structure of limk1 mutant d460n in complex with full-length cofilin-1 |
|
75
|
285
|
5hx6A |
Crystal structure of rip1 kinase with a benzo[b][1,4]oxazepin-4-one |
|
217
|
633
|
5hyxB |
Plant peptide hormone receptor rgfr1 in complex with rgf1 |
|
125
|
400
|
5hvuA |
Rho-associated protein kinase 1 (rock 1) in complex with a pyridine thiazole piperidine inhibitor |
|
115
|
328
|
5htbA |
Crystal structure of haspin (gsg2) in complex with bisubstrate inhibitor arc-3353 |
|
81
|
289
|
5ho7A |
Discovery of novel 7-azaindoles as pdk1 inhibitors |
|
118
|
328
|
5htcA |
Crystal structure of haspin (gsg2) in complex with bisubstrate inhibitor arc-3372 |
|
338
|
1157
|
5flcB |
Architecture of human mtor complex 1 - 5.9 angstrom reconstruction |
|
103
|
351
|
5hlnA |
X-ray crystal structure of gsk3b in complex with chir99021 |
|
340
|
1061
|
5fi4A |
Discovery of imidazo[1,2-a]-pyridine inhibitors of pan-pi3 kinases that are efficacious in a mouse xenograft model |
|
251
|
710
|
5gr8A |
Crystal structure of pepr1-atpep1 |
|
75
|
269
|
5hieA |
Braf kinase domain b3ac loop deletion mutant in complex with dabrafenib |
|
265
|
942
|
5edsA |
Crystal structure of human pi3k-gamma in complex with benzimidazole inhibitor 5 |
|
321
|
1061
|
5dxhA |
P110alpha/p85alpha with compound 5 |
|
91
|
294
|
4usfA |
Human slk with sb-440719 |
|
77
|
293
|
4useA |
Human stk10 (lok) with sb-633825 |
|
258
|
948
|
4urkA |
Pi3kg in complex with azd6482 |
|
1
|
10
|
4chbC |
Crystal structure of the human klhl2 kelch domain in complex with a wnk4 peptide |
|
1
|
9
|
4ch9C |
Crystal structure of the human klhl3 kelch domain in complex with a wnk4 peptide |
|
588
|
2643
|
5yz0A |
Cryo-em structure of human atr-atrip complex |
|
74
|
265
|
6hjkA |
Crystal structure of aurora-a l210c catalytic domain in complex with asdo2 |
|
84
|
267
|
6hjjA |
Crystal structure of aurora-a l210c catalytic domain in complex with asdo6 ligand |
|
65
|
276
|
6h0oA |
Nek2 bound to purine inhibitor |
|
0
|
11
|
6gy5U |
Crystal structure of the kelch domain of human klhl20 in complex with dapk1 peptide |
|
79
|
301
|
6gttA |
Human stk10 bound to birb-796 |
|
94
|
291
|
6gzmA |
Crystal structure of human ckidelta with a86 |
|
243
|
942
|
6gq7A |
Pi3kg in complex with inh |
|
99
|
297
|
6gzdA |
Crystal structure of human csnk1a1 with a86 |
|
67
|
280
|
6gt1A |
Nek7 bound to purine inhibitor |
|
102
|
293
|
6groA |
Human csnk1g3 bound to sb-223133 |
|
92
|
348
|
6gn1A |
Crystal structure of glycogen synthase kinase-3 beta (gsk3b) in complex with pik-75 |
|
113
|
327
|
6gihA |
Crystal structure of ck2alpha with cam187 bound |
|
108
|
325
|
6gmdA |
The crystal structure of ck2alpha in complex with compound 3 |
|
116
|
327
|
6g34A |
Crystal structure of haspin in complex with 5-iodotubercidin |
|
112
|
327
|
6g38A |
Crystal structure of haspin in complex with tubercidin |
