|
110
|
325
|
4dgoA |
Crystal structure of maize ck2 in complex with tyrphostin ag99 |
|
93
|
302
|
4czuA |
Crystal structure of the kinase domain of cipk23 t190d mutant |
|
93
|
341
|
4crsA |
Human protein kinase n2 (pkn2, prkcl2) in complex with atpgammas |
|
94
|
295
|
4dbxA |
Crystal structure of aminoglycoside phosphotransferase aph(2")-id/aph(2")-iva |
|
83
|
272
|
4d4rA |
Focal adhesion kinase catalytic domain |
|
110
|
326
|
4dgnA |
Crystal structure of maize ck2 in complex with the inhibitor luteolin |
|
75
|
262
|
4dhfA |
Structure of aurora a mutant bound to biogenidec cpd 15 |
|
98
|
309
|
4ctbA |
Structure of the human anaplastic lymphoma kinase in complex with the inhibitor (5r)-8-amino-3-fluoro-5,19-dimethyl-20-oxo-5,18,19,20- tetrahydro-7,11-(azeno)pyrido(2',1':2,3)imidazo(4,5-h)(2,5,11) benzoxadiazacyclotetradecine-14-carbonitrile |
|
76
|
264
|
4debA |
Aurora a in complex with rk2-17-01 |
|
101
|
334
|
4dglC |
Crystal structure of the ck2 tetrameric holoenzyme |
|
82
|
278
|
4dggA |
C-src kinase domain in complex with rm-1-176 |
|
86
|
272
|
4d5kA |
Focal adhesion kinase catalytic domain |
|
87
|
294
|
4dehA |
Crystal structure of c-met in complex with triazolopyridinone inhibitor 3 |
|
103
|
292
|
4d0wA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
94
|
337
|
4dfyA |
Crystal structure of r194a mutant of camp-dependent protein kinase with unphosphorylated activation loop |
|
94
|
289
|
4d1sA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
104
|
351
|
4dljA |
Human p38 map kinase in complex with rl163 |
|
72
|
279
|
4cv8A |
Mps1 kinase with 3-aminopyridin-2-one inhibitors |
|
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 |
|
90
|
248
|
4dhjA |
The structure of a ceotub1 ubiquitin aldehyde ubc13~ub complex |
|
78
|
284
|
4ct1A |
Human pdk1-pkczeta kinase chimera in complex with allosteric compound ps315 bound to the pif-pocket |
|
110
|
336
|
4dh1A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with low mg2+, atp and ip20 |
|
73
|
281
|
4d2sA |
Human ttk in complex with a dyrk1b inhibitor |
|
109
|
336
|
4dh7A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with high mg2+, amp-pnp and ip20' |
|
82
|
273
|
4d55A |
Focal adhesion kinase catalytic domain |
|
79
|
272
|
4d5hA |
Focal adhesion kinase catalytic domain |
|
87
|
238
|
4dhiB |
Structure of c. elegans otub1 bound to human ubc13 |
|
98
|
293
|
4d0xA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
98
|
299
|
4dfbA |
Crystal structure of aminoglycoside phosphotransferase aph(2")-id/aph(2")-iva in complex with kanamycin |
|
106
|
344
|
4dn5A |
Crystal structure of nf-kb-inducing kinase (nik) |
|
87
|
294
|
4deiA |
Crystal structure of c-met in complex with triazolopyridinone inhibitor 24 |
|
113
|
350
|
4dfxE |
Crystal structure of myristoylated k7c catalytic subunit of camp-dependent protein kinase in complex with sp20 and amp-pnp |
|
76
|
265
|
4csvA |
Tyrosine kinase as - a common ancestor of src and abl bound to gleevec |
|
105
|
296
|
4dcaA |
Crystal structure of aminoglycoside phosphotransferase aph(2'')-ib, adp-bound |
|
112
|
350
|
4dfzE |
Crystal structure of myristoylated k7c catalytic subunit of camp-dependent protein kinase in complex with sp20 |
|
96
|
339
|
4dc2A |
Structure of pkc in complex with a substrate peptide from par-3 |
|
107
|
341
|
4dg0E |
Crystal structure of myristoylated wt catalytic subunit of camp-dependent protein kinase in complex with sp20 and amp-pnp |
|
81
|
272
|
4d4yA |
Focal adhesion kinase catalytic domain |
|
81
|
273
|
4d58A |
Focal adhesion kinase catalytic domain in complex with bis-anilino pyrimidine inhibitor |
|
117
|
399
|
4ddgA |
Crystal structure of human otub1/ubch5b~ub/ub |
|
80
|
333
|
4cxaA |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
|
90
|
296
|
4de4A |
Crystal structure of aminoglycoside phosphotransferase aph(2")-id/aph(2")-iva in complex with hepes |
|
75
|
272
|
4cqeA |
B-raf kinase v600e mutant in complex with a diarylthiazole b-raf inhibitor |
|
91
|
310
|
4dceA |
Crystal structure of human anaplastic lymphoma kinase in complex with a piperidine-carboxamide inhibitor |
|
86
|
271
|
4deeA |
Aurora a in complex with adp |
|
82
|
272
|
4d4vA |
Focal adhesion kinase catalytic domain |
|
110
|
326
|
4dgmA |
Crystal structure of maize ck2 in complex with the inhibitor apigenin |
|
91
|
256
|
4dhzA |
The structure of h/ceotub1-ubiquitin aldehyde-ubc13~ub |
|
95
|
302
|
4d2rA |
Human igf in complex with a dyrk1b inhibitor |
|
83
|
274
|
4dfnA |
Crystal structure of spleen tyrosine kinase complexed with an adamantylpyrazine inhibitor |
