|
78
|
294
|
4equA |
Human stk-10 (lok) kinase domain in dfg-out conformation with inhibitor dsa-7 |
|
91
|
300
|
4eopA |
Thr 160 phosphorylated cdk2 q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
91
|
302
|
4e5wA |
Jak1 kinase (jh1 domain) in complex with compound 26 |
|
92
|
334
|
4ekkA |
Akt1 with amp-pnp |
|
93
|
293
|
4dymA |
Crystal structure of the acvr1 kinase domain in complex with the imidazo[1,2-b]pyridazine inhibitor k00135 |
|
73
|
276
|
4ehgA |
B-raf kinase domain in complex with an aminopyridimine-based inhibitor |
|
85
|
300
|
4eonA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
78
|
269
|
4enxA |
Crystal structure of pim-1 kinase in complex with inhibitor (2e,5z)-2-(2-chlorophenylimino)-5-(4-hydroxy-3-nitrobenzylidene)thiazolidin-4-one |
|
109
|
348
|
4e6aA |
P38a-pia23 complex |
|
104
|
351
|
4eh6A |
Human p38 map kinase in complex with np-f5 and rl87 |
|
82
|
298
|
4eorA |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
|
88
|
298
|
4eolA |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with the inhibitor ro3306 |
|
88
|
298
|
4el9A |
Structure of n-terminal kinase domain of rsk2 with afzelin |
|
72
|
276
|
4eheA |
B-raf kinase domain in complex with an aminothienopyrimidine-based inhibitor |
|
83
|
273
|
4dtkA |
Novel and selective pan-pim kinase inhibitor |
|
95
|
297
|
4eqcA |
Crystal structure of pak1 kinase domain in complex with frax597 inhibitor |
|
81
|
276
|
4ebwA |
Structure of focal adhesion kinase catalytic domain in complex with novel allosteric inhibitor |
|
104
|
348
|
4e6cA |
P38a-perifosine complex |
|
85
|
299
|
4eoiA |
Thr 160 phosphorylated cdk2 k89d, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
105
|
351
|
4e5aX |
The w197a mutant of p38a map kinase |
|
89
|
302
|
4e4nA |
Jak1 kinase (jh1 domain) in complex with compound 49 |
|
87
|
296
|
4ek3A |
Crystal structure of apo cdk2 |
|
84
|
302
|
4ei4A |
Jak1 kinase (jh1 domain) in complex with compound 20 |
|
111
|
348
|
4ehvA |
Human p38 map kinase in complex with np-f10 and rl87 |
|
83
|
299
|
4eomA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with atp |
|
84
|
302
|
4eevA |
Crystal structure of c-met in complex with ly2801653 |
|
69
|
274
|
4e4xA |
Crystal structure of b-raf kinase domain in complex with a dihydropyrido[2,3-d]pyrimidinone-based inhibitor |
|
76
|
276
|
4e26A |
Braf in complex with an organic inhibitor 7898734 |
|
104
|
350
|
4eh9A |
Human p38 map kinase in complex with np-f11 and rl87 |
|
106
|
344
|
4dn5A |
Crystal structure of nf-kb-inducing kinase (nik) |
|
76
|
265
|
4csvA |
Tyrosine kinase as - a common ancestor of src and abl bound to gleevec |
|
73
|
281
|
4d2sA |
Human ttk in complex with a dyrk1b inhibitor |
|
113
|
350
|
4dfxE |
Crystal structure of myristoylated k7c catalytic subunit of camp-dependent protein kinase in complex with sp20 and amp-pnp |
|
103
|
333
|
4d2wA |
Structure of melk in complex with inhibitors |
|
114
|
412
|
4czyB |
Complex of neurospora crassa pan2 (wd40-cs1) with pan3 (pseudokinase and c-term) |
|
110
|
326
|
4dgnA |
Crystal structure of maize ck2 in complex with the inhibitor luteolin |
|
98
|
293
|
4d0xA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
75
|
262
|
4dhfA |
Structure of aurora a mutant bound to biogenidec cpd 15 |
|
89
|
299
|
4d9tA |
Rsk2 c-terminal kinase domain with inhibitor (e)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate |
|
92
|
308
|
4ctcA |
Structure of the human anaplastic lymphoma kinase in complex with the inhibitor 7-amino-3-cyclopropyl-12-fluoro-1,10,16-trimethyl-16,17- dihydro-1h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecin-15(10h)-one |
|
110
|
350
|
4dliA |
Human p38 map kinase in complex with rl87 |
|
81
|
272
|
4d4yA |
Focal adhesion kinase catalytic domain |
|
101
|
334
|
4dglC |
Crystal structure of the ck2 tetrameric holoenzyme |
|
103
|
292
|
4d0wA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
82
|
278
|
4dggA |
C-src kinase domain in complex with rm-1-176 |
|
87
|
294
|
4dehA |
Crystal structure of c-met in complex with triazolopyridinone inhibitor 3 |
|
74
|
293
|
4d1zA |
Cdk2 in complex with a luciferin derivate |
|
93
|
341
|
4crsA |
Human protein kinase n2 (pkn2, prkcl2) in complex with atpgammas |
|
82
|
273
|
4d55A |
Focal adhesion kinase catalytic domain |
|
110
|
336
|
4dh1A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with low mg2+, atp and ip20 |
