|
88
|
340
|
6v2yB |
Crystal structure of the braf:mek1 kinases in complex with amppnp and trametinib |
|
48
|
310
|
6wjgA |
Pka riibeta holoenzyme with dnajb1-pkac fusion in fibrolamellar hepatoceullar carcinoma |
|
98
|
361
|
6tpaA |
Cdk8/cyclinc in complex with drug etp-50775 |
|
89
|
342
|
6v32B |
Crystal structure of the braf:mek1 kinases in complex with amppnp and selumetinib |
|
108
|
338
|
6ypsA |
Crystal structure of the camp-dependent protein kinase a in complex with 4-hydroxybenzamidine |
|
123
|
333
|
6tlrA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,7-dibromobenzotriazole |
|
122
|
333
|
6tlpA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole |
|
123
|
333
|
6tllA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6,7-tetrabromobenzotriazole (tbbt) |
|
91
|
276
|
7ccwA |
Crystal structure of death-associated protein kinase 1 in complex with resveratrol and mes |
|
85
|
276
|
7ccvA |
Crystal structure of death-associated protein kinase 1 in complex with piceatannol |
|
79
|
267
|
6sg4A |
Structure of cdk2/cyclin a m246q, s247en |
|
58
|
442
|
7kpvA |
Structure of kinase and central lobes of yeast ckm |
|
88
|
276
|
7ccuA |
Crystal structure of death-associated protein kinase 1 in complex with resveratrol |
|
58
|
442
|
7kpxA |
Structure of the yeast ckm |
|
88
|
343
|
7juyC |
Crystal structure of ksr1:mek1 in complex with amp-pnp, and allosteric mek inhibitor cobimetinib |
|
110
|
393
|
7jntA |
Crystal structure of rho-associated protein kinase 2 (rock2) in complex with a potent and selective dual rock inhibitor |
|
96
|
394
|
7jouA |
Crystal structure of rho-associated protein kinase 1 (rock1) in complex with a phenylpyrazole amide inhibitor |
|
103
|
393
|
7jovA |
Crystal structure of rho-associated protein kinase 2 (rock2) in complex with a phenylpyrazole amide inhibitor |
|
325
|
1196
|
6vp8A |
Cryo-em structure of the c-terminal half of the parkinson's disease-linked protein leucine rich repeat kinase 2 (lrrk2) |
|
113
|
338
|
6zlnA |
Clk1 bound with gw807982x (cpd 8) |
|
328
|
1196
|
6vnoA |
Cryo-em structure of the c-terminal half of the parkinson's disease-linked protein leucine rich repeat kinase 2 (lrrk2) |
|
328
|
1196
|
6vp6A |
Cryo-em structure of the c-terminal half of the parkinson's disease-linked protein leucine rich repeat kinase 2 (lrrk2) |
|
325
|
1196
|
6vp7A |
Cryo-em structure of the c-terminal half of the parkinson's disease-linked protein leucine rich repeat kinase 2 (lrrk2) |
|
105
|
331
|
6wppA |
Human nik in complex with ligand compound x |
|
107
|
350
|
6zwpA |
P38a bound with sr348 |
|
112
|
349
|
6zwrA |
P38a bound with sr92 |
|
105
|
364
|
7cmlA |
The crystal structure of human jnk2 from wuxi biortus. |
|
88
|
304
|
6yz4A |
Crystal structure of mkk7 (map2k7) with ibrutinib bound at allosteric site |
|
86
|
299
|
6yg4A |
Crystal structure of mkk7 (map2k7) in complex with k00007 |
|
92
|
303
|
6yg2A |
Crystal structure of mkk7 (map2k7) in complex with ibrutnib, with covalent and allosteric binding modes |
|
83
|
270
|
6xihA |
Structure-guided optimization of a novel class of ask1 inhibitors with increased sp3 character and an exquisite selectivity profile |
|
88
|
301
|
6yg6A |
Crystal structure of mkk7 (map2k7) covalently bound with type-ii inhibitor tl10-105 |
|
82
|
302
|
6yg7A |
Crystal structure of mkk7 (map2k7) covalently bound with type-ii inhibitor sb1-g-23 |
|
85
|
301
|
6yg0A |
Crystal structure of s287d,t291d mkk7 (map2k7), apo form |
|
85
|
298
|
6yg3A |
Crystal structure of mkk7 (map2k7) covalently bound with cpt1-70-1 |
|
93
|
307
|
6yfzA |
Crystal structure of mkk7 (map2k7), apo form |
|
100
|
319
|
6yg1A |
Crystal structure of mkk7 (map2k7) in an active state, allosterically triggered by the n-terminal helix |
|
75
|
303
|
6yg5A |
Crystal structure of mkk7 (map2k7) in complex with asc69 |
|
74
|
277
|
6sgiA |
Nek2 kinase bound to inhibitor 96 |
|
73
|
277
|
6sgkA |
Nek2 kinase bound to inhibitor 102 |
|
80
|
273
|
6l11A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
77
|
273
|
6l13A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
83
|
273
|
6l12A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
79
|
273
|
6l15A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
79
|
273
|
6l16A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
80
|
273
|
6l14A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
105
|
330
|
6k77A |
Crystal structure of amppnp bound ck1a alpha from c. neoformans |
|
107
|
330
|
6k74A |
Crystal structure of amppnp bound ck1a alpha from c. neoformans |
|
110
|
348
|
5ra7A |
Pandda analysis group deposition form1 map kinase p38-alpha -- fragment n11351a in complex with map kinase p38-alpha |
|
107
|
348
|
5r9yA |
Pandda analysis group deposition form1 map kinase p38-alpha -- fragment n13619a in complex with map kinase p38-alpha |
