|
195
|
659
|
4iwpA |
Crystal structure and mechanism of activation of tbk1 |
|
70
|
275
|
4jvgA |
B-raf kinase in complex with birb796 |
|
90
|
302
|
4ivbA |
Jak1 kinase (jh1 domain) in complex with the inhibitor trans-4-{2-[(1r)-1-hydroxyethyl]imidazo[4,5-d]pyrrolo[2,3-b]pyridin-1(6h)-yl}cyclohexanecarbonitrile |
|
95
|
290
|
4jdhA |
Crystal structure of serine/threonine-protein kinase pak 4 in complex with paktide t peptide substrate |
|
78
|
274
|
4jx3A |
Crystal structure of pim1 kinase |
|
212
|
659
|
4im2A |
Structure of tank-binding kinase 1 |
|
70
|
279
|
4js8A |
Crystal structure of ttk kinase domain with an inhibitor: 401348 |
|
91
|
298
|
4j95A |
Crystal structure of fgf receptor 2 (fgfr2) kinase domain harboring the pathogenic k659n mutation responsible for an unclassified craniosynostosis syndrome in space group c2. |
|
86
|
324
|
4jq8A |
Crystal structure of egfr kinase domain in complex with compound 4b |
|
88
|
290
|
4ji9A |
Jak2 kinase (jh1 domain) in complex with tg101209 |
|
90
|
315
|
4i22A |
Structure of the monomeric (v948r)gefitinib/erlotinib resistant double mutant (l858r+t790m) egfr kinase domain co-crystallized with gefitinib |
|
107
|
336
|
4iayA |
Room temperature x-ray structure of camp dependent protein kinase a in complex with high sr2+ concentration, adp and phosphorylated peptide psp20 |
|
116
|
348
|
4izaA |
Structure of dually phosphorylated erk2 bound to the pea-15 death effector domain |
|
108
|
338
|
4ib1A |
Structure of camp dependent protein kinase a in complex with high k+ concentration, adp and phosphorylated peptide psp20 |
|
105
|
346
|
4ix4A |
Crystal structure of a stt7 homolog from micromonas algae in complex with adp |
|
89
|
300
|
4jiaA |
Jak2 kinase (jh1 domain) in complex with compound 9 |
|
90
|
297
|
4k33A |
Crystal structure of fgf receptor 3 (fgfr3) kinase domain harboring the k650e mutation, a gain-of-function mutation responsible for thanatophoric dysplasia type ii and spermatocytic seminoma |
|
88
|
302
|
4ivcA |
Jak1 kinase (jh1 domain) in complex with the inhibitor (trans-4-{2-[(1r)-1-hydroxyethyl]imidazo[4,5-d]pyrrolo[2,3-b]pyridin-1(6h)-yl}cyclohexyl)acetonitrile |
|
193
|
660
|
4iwoA |
Crystal structure and mechanism of activation of tbk1 |
|
68
|
280
|
4jt3A |
Crystal structure of ttk kinase domain with an inhibitor: 400740 |
|
101
|
362
|
4jrnA |
Rop18 kinase domain in complex with amp-pnp and sucrose |
|
84
|
284
|
4i5pA |
Selective & brain-permeable polo-like kinase-2 (plk-2) inhibitors that reduce -synuclein phosphorylation in rat brain |
|
152
|
464
|
4ifgA |
Crystal structure of tgcdpk1 with inhibitor bound |
|
208
|
659
|
4im0A |
Structure of tank-binding kinase 1 |
|
85
|
324
|
4jr3A |
Crystal structure of egfr kinase domain in complex with compound 3g |
|
45
|
205
|
4jmqA |
Crystal structure of pb9: the dit of bacteriophage t5. |
|
75
|
285
|
4i6hA |
Selective & brain-permeable polo-like kinase-2 (plk-2) inhibitors that reduce alpha-synuclein phosphorylation in rat brain |
|
109
|
337
|
4ie9A |
Bovine pka c-alpha in complex with 3-pyridylmethyl-5-methyl-1h-pyrazole-3-carboxylate |
|
93
|
290
|
4jdjA |
Crystal structure of serine/threonine-protein kinase pak 4 f461v mutant in complex with paktide t peptide substrate |
|
83
|
274
|
4k0yA |
Structure of pim-1 kinase bound to n-(4-fluorophenyl)-7-hydroxy-5-(piperidin-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide |
|
83
|
269
|
4hyhA |
X-ray crystal structure of compound 39 bound to human chk1 kinase domain |
|
110
|
337
|
4iazA |
Structure of camp dependent protein kinase a in complex with high ba2+ concentration, adp and phosphorylated peptide psp20 |
|
92
|
292
|
4ivaA |
Jak2 kinase (jh1 domain) in complex with the inhibitor trans-4-[(8as)-2-[(1r)-1-hydroxyethyl]imidazo[4,5-d]pyrrolo[2,3-b]pyridin-1(8ah)-yl]cyclohexanecarbonitrile |
|
161
|
464
|
4ihpA |
Crystal structure of tgcdpk1 with inhibitor bound |
|
160
|
463
|
4jbvA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1268 |
|
76
|
265
|
4jaiA |
Crystal structure of aurora kinase a in complex with n-{4-[(6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-yl)amino]phenyl}benzamide |
|
81
|
292
|
4joaA |
Crystal structure of human anaplastic lymphoma kinase in complex with 7-azaindole based inhibitor |
|
83
|
285
|
4i6fA |
Selective & brain-permeable polo-like kinase-2 (plk-2) inhibitors that reduce -synuclein phosphorylation in rat brain |
|
99
|
348
|
4j71A |
Crystal structure of gsk3b in complex with inhibitor 1r |
|
94
|
297
|
4i94A |
Structure of bsk8 in complex with amp-pnp |
|
92
|
277
|
4i0rA |
Crystal structure of spleen tyrosine kinase complexed with 2-(3,4,5-trimethoxy-phenyl)-5h-pyrrolo[2,3-b]pyrazine-7-carboxylic acid isopropylamide |
|
85
|
273
|
4hzrA |
Crystal structure of ack1 kinase domain |
|
108
|
337
|
4iadA |
Low temperature x-ray structure of camp dependent protein kinase a in complex with high mg2+ concentration, adp and phosphorylated peptide psp20 |
|
94
|
290
|
4jdiA |
Crystal structure of serine/threonine-protein kinase pak 4 in complex with paktide s peptide substrate |
|
78
|
287
|
4itiA |
Crystal structure of rip1 kinase in complex with necrostatin-3 analog |
|
100
|
304
|
4j98A |
Crystal structure of fgf receptor 2 (fgfr2) kinase domain harboring the gain-of-function k659q mutation. |
|
194
|
659
|
4im3A |
Structure of tank-binding kinase 1 |
|
85
|
272
|
4i4fA |
Structure of focal adhesion kinase catalytic domain in complex with an allosteric binding pyrazolobenzothiazine compound. |
|
104
|
337
|
4ij9A |
Bovine pka c-alpha in complex with 2-[[5-(4-pyridyl)-1h-1,2,4-triazol-3-yl]sulfanyl]-1-(2-thiophenyl)ethanone |
|
86
|
324
|
4jq7A |
Crystal structure of egfr kinase domain in complex with compound 2a |
