|
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 |
|
97
|
354
|
4hyuA |
Crystal structure of jnk1 in complex with jip1 peptide and 4-{4-[4-(3-methanesulfonyl-propoxy)-indazol-1-yl]-pyrimidin-2-ylamino}-cyclohexan |
|
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 |
|
82
|
266
|
4jbqA |
Novel aurora kinase inhibitors reveal mechanisms of hurp in nucleation of centrosomal and kinetochore microtubules |
|
70
|
275
|
4jvgA |
B-raf kinase in complex with birb796 |
|
81
|
265
|
4jajA |
Crystal structure of aurora kinase a in complex with benzo[c][1,8]naphthyridin-6(5h)-one |
|
78
|
274
|
4jx3A |
Crystal structure of pim1 kinase |
|
70
|
279
|
4js8A |
Crystal structure of ttk kinase domain with an inhibitor: 401348 |
|
86
|
324
|
4jq8A |
Crystal structure of egfr kinase domain in complex with compound 4b |
|
85
|
273
|
4i4eA |
Structure of focal adhesion kinase catalytic domain in complex with hinge binding pyrazolobenzothiazine compound. |
|
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 |
|
105
|
347
|
4iz5A |
Structure of the complex between erk2 phosphomimetic mutant and pea-15 |
|
98
|
297
|
4jjrA |
A p21 crystal form of mammalian casein kinase 1 delta |
|
108
|
338
|
4ib1A |
Structure of camp dependent protein kinase a in complex with high k+ concentration, adp and phosphorylated peptide psp20 |
|
106
|
346
|
4ix6A |
Crystal structure of a stt7 homolog from micromonas algae soaked with atp |
|
86
|
309
|
4jg7A |
Structure of rsk2 ctd bound to 3-(3-(1h-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)-2-cyanoacrylamide |
|
83
|
289
|
4i93A |
Structure of the bsk8 kinase domain (semet labeled) |
|
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 |
|
75
|
287
|
4ithA |
Crystal structure of rip1 kinase in complex with necrostatin-1 analog |
|
71
|
266
|
4j8nA |
Aurora a kinase apo |
|
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 |
|
91
|
297
|
4j97A |
Crystal structure of fgf receptor 2 (fgfr2) kinase domain harboring the pathogenic gain-of-function k659e mutation identified in endometrial cancer. |
|
86
|
324
|
4i23A |
Crystal structure of the wild-type egfr kinase domain in complex with dacomitinib (soaked) |
|
99
|
301
|
4ibmA |
Crystal structure of insulin receptor kinase domain in complex with an inhibitor irfin-1 |
|
95
|
354
|
4izyA |
Crystal structure of jnk1 in complex with jip1 peptide and 4-{4-[4-(4-methanesulfonyl-piperidin-1-yl)-indol-1-yl]-pyrimidin-2-ylamino}-cyclohexan |
|
109
|
337
|
4ie9A |
Bovine pka c-alpha in complex with 3-pyridylmethyl-5-methyl-1h-pyrazole-3-carboxylate |
|
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 |
|
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 |
|
84
|
266
|
4jboA |
Novel aurora kinase inhibitors reveal mechanisms of hurp in nucleation of centrosomal and kinetochore microtubules |
|
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 |
|
161
|
464
|
4ihpA |
Crystal structure of tgcdpk1 with inhibitor bound |
|
99
|
306
|
4j96A |
Crystal structure of fgf receptor 2 (fgfr2) kinase domain harboring the pathogenic gain-of-function k659m mutation identified in cervical cancer. |
|
160
|
463
|
4jbvA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1268 |
|
82
|
294
|
4j7bA |
Crystal structure of polo-like kinase 1 |
|
81
|
292
|
4joaA |
Crystal structure of human anaplastic lymphoma kinase in complex with 7-azaindole based inhibitor |
|
92
|
287
|
4i1zA |
Crystal structure of the monomeric (v948r) form of the gefitinib/erlotinib resistant egfr kinase domain l858r+t790m |
|
94
|
297
|
4i94A |
Structure of bsk8 in complex with amp-pnp |
|
115
|
350
|
4iz7A |
Structure of non-phosphorylated erk2 bound to the pea-15 death effector domain |
|
78
|
307
|
4jg6A |
Rsk2 ctd bound to 2-cyano-3-(1h-indazol-5-yl)acrylamide |
|
89
|
277
|
4i0tA |
Crystal structure of spleen tyrosine kinase complexed with 2-(5,6,7,8-tetrahydro-imidazo[1,5-a]pyridin-1-yl)-5h-pyrrolo[2,3-b]pyrazine-7-carboxylic acid tert-butylamide |
|
107
|
334
|
4ixpA |
Crystal structure of maternal embryonic leucine zipper kinase (melk) |
|
83
|
272
|
4hyiA |
X-ray crystal structure of compound 40 bound to human chk1 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 |
|
78
|
287
|
4itiA |
Crystal structure of rip1 kinase in complex with necrostatin-3 analog |
|
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 |
|
194
|
659
|
4im3A |
Structure of tank-binding kinase 1 |
