|
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 |
|
83
|
289
|
4i93A |
Structure of the bsk8 kinase domain (semet labeled) |
|
91
|
332
|
4hzsA |
Crystal structure of ack1 kinase domain with c-terminal sh3 domain |
|
75
|
287
|
4ithA |
Crystal structure of rip1 kinase in complex with necrostatin-1 analog |
|
85
|
265
|
4jbpA |
Novel aurora kinase inhibitors reveal mechanisms of hurp in nucleation of centrosomal and kinetochore microtubules |
|
72
|
273
|
4id7A |
Ack1 kinase in complex with the inhibitor cis-3-[8-amino-1-(4-phenoxyphenyl)imidazo[1,5-a]pyrazin-3-yl]cyclobutanol |
|
94
|
336
|
4ijpA |
Crystal structure of human prpf4b kinase domain in complex with 4-{5-[(2-chloro-pyridin-4-ylmethyl)-carbamoyl]-thiophen-2-yl}-benzo[b]thiophene-2-carboxylic acid amine |
|
76
|
266
|
4j8mA |
Aurora a in complex with cd532 |
|
91
|
296
|
4i3zA |
Structure of pcdk2/cyclina bound to adp and 2 magnesium ions |
|
99
|
301
|
4ibmA |
Crystal structure of insulin receptor kinase domain in complex with an inhibitor irfin-1 |
|
85
|
293
|
4j53A |
Crystal structure of plk1 in complex with tak-960 |
|
96
|
348
|
4j1rA |
Crystal structure of gsk3b in complex with inhibitor 15r |
|
80
|
300
|
4jg8A |
Structure of rsk2 t493m ctd mutant bound to 2-cyano-n-(1-hydroxy-2-methylpropan-2-yl)-3-(3-(3,4,5-trimethoxyphenyl)-1h-indazol-5-yl)acrylamide |
|
82
|
287
|
4i20A |
Crystal structure of monomeric (v948r) primary oncogenic mutant l858r egfr kinase domain |
|
93
|
290
|
4jdjA |
Crystal structure of serine/threonine-protein kinase pak 4 f461v mutant in complex with paktide t peptide substrate |
|
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 |
|
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 |
|
161
|
464
|
4ihpA |
Crystal structure of tgcdpk1 with inhibitor bound |
|
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 |
|
160
|
463
|
4jbvA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1268 |
|
99
|
348
|
4j71A |
Crystal structure of gsk3b in complex with inhibitor 1r |
|
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 |
|
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 |
|
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 |
|
85
|
273
|
4hzrA |
Crystal structure of ack1 kinase domain |
|
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. |
|
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 |
|
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. |
|
111
|
345
|
4idvA |
Crystal structure of nik with compound 4-{3-[2-amino-5-(2-methoxyethoxy)pyrimidin-4-yl]-1h-indol-5-yl}-2-methylbut-3-yn-2-ol (13v) |
|
86
|
324
|
4jq7A |
Crystal structure of egfr kinase domain in complex with compound 2a |
|
77
|
317
|
4i21A |
Crystal structure of l858r + t790m egfr kinase domain in complex with mig6 peptide |
|
98
|
338
|
4ifcA |
Crystal structure of adp-bound human prpf4b kinase domain |
|
197
|
658
|
4iw0A |
Crystal structure and mechanism of activation of tbk1 |
|
88
|
289
|
4i92A |
Structure of the bsk8 kinase domain |
|
104
|
346
|
4ix3A |
Crystal structure of a stt7 homolog from micromonas algae |
|
83
|
269
|
4jikA |
X-ray crystal structure of compound 22a (r)-2-(4-chlorophenyl)-8-(piperidin-3-ylamino)imidazo[1,2-c]pyrimidine-5-carboxamide bound to human chk1 kinase domain |
|
107
|
336
|
4iaiA |
X-ray structure of camp dependent protein kinase a in complex with high ca2+ concentration, adp and phosphorylated peptide psp20 |
|
93
|
305
|
4iwdA |
Structure of dually phosphorylated c-met receptor kinase in complex with an mk-8033 analog |
|
84
|
287
|
4itjA |
Crystal structure of rip1 kinase in complex with necrostatin-4 |
|
84
|
266
|
4jboA |
Novel aurora kinase inhibitors reveal mechanisms of hurp in nucleation of centrosomal and kinetochore microtubules |
|
131
|
372
|
4jr7A |
Crystal structure of scck2 alpha in complex with gmppnp |
