|
89
|
289
|
7m0kA |
Hpk1 in complex with compound 1 |
|
114
|
347
|
6yf8A |
Dyrk1a with pst001 |
|
96
|
293
|
7m0mA |
Hpk1 in complex with compound 1 |
|
82
|
287
|
7l24A |
Hpk1 in complex with compound 11 |
|
85
|
287
|
7l26A |
Hpk1 in complex with compound 38 |
|
112
|
349
|
7be5A |
Crystal structure of map kinase p38 alpha in complex with inhibitor sr276 |
|
100
|
356
|
7kskA |
Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors |
|
101
|
349
|
7be4A |
Crystal structure of map kinase p38 alpha in complex with inhibitor sr159 |
|
97
|
312
|
7b9lA |
Mek1 in complex with compound 23 |
|
194
|
1347
|
7bl1CCC |
Human complex ii-bats bound to membrane-attached rab5a-gtp |
|
93
|
312
|
7b94A |
Mek1 in complex with compound 6 |
|
100
|
349
|
7bdoA |
Mapk14 bound with sr302 |
|
91
|
288
|
7l25A |
Hpk1 in complex with compound 18 |
|
109
|
349
|
7bdqA |
Mapk14 bound with sr300 |
|
97
|
312
|
7b3mA |
Mek1 in complex with compound 6 |
|
94
|
312
|
7b7rA |
Mek1 in complex with compound 4 |
|
115
|
355
|
7ncfA |
Crystal structure of hipk2 in complex with mu135 (compound 21e) |
|
106
|
322
|
6vxuA |
Structure of human vaccinia-related kinase 1 (vrk1) bound to ach471 |
|
105
|
356
|
7ksiA |
Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors |
|
109
|
353
|
6y0bA |
Crystal structure of the camp-dependent protein kinase a cocrystallized with quinazolin-4-amine and pki (5-24) |
|
111
|
344
|
6y05A |
Crystal structure of the camp-dependent protein kinase a cocrystallized with adenine and pki (5-24) |
|
102
|
365
|
6y0aA |
Crystal structure of cdk8-cycc in complex with bi00690300 |
|
115
|
332
|
7b8iA |
Tetragonal structure of human protein kinase ck2 catalytic subunit in complex with a heparin oligo saccharide |
|
221
|
706
|
6m13a |
Crystal structure of rnase l in complex with toceranib |
|
106
|
314
|
6kmhA |
The crystal structure of cask/mint1 complex |
|
79
|
273
|
6l17A |
Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives |
|
217
|
706
|
6m12a |
Crystal structure of rnase l in complex with su11652 |
|
209
|
706
|
6m11a |
Crystal structure of rnase l in complex with sunitinib |
|
78
|
289
|
6vpjA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 c247v + c319v double mutant dephosphorylated, and in complex with amp-pnp |
|
74
|
262
|
6xkaA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 dephosphorylated, and coalated on c290 |
|
90
|
289
|
6vpmA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 with c290 disulfide bonded to compound 8-34, and in complex with amp-pnp |
|
79
|
290
|
6vphA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 modified with cacodylate and in complex with amp-pnp |
|
90
|
289
|
6vplA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 with c290 disulfide bonded to compound 7-80, and in complex with amp-pnp |
|
84
|
288
|
6vpiA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 c247v + d256n + c319v triple mutant disulfide homodimer in complex with amp-pnp |
|
85
|
288
|
6vpgA |
Tpx2 residues 7-20 fused to aurora a residues 116-389 in complex with amp-pnp |
|
184
|
542
|
6pjxA |
Crystal structure of g protein-coupled receptor kinase 5 (grk5) in complex with calmodulin (cam) |
|
114
|
328
|
7a22A |
Crystal structure of human protein kinase ck2alpha' (csnk2a2 gene product) in complex with the atp-competitive inhibitor 5,6,7-tribromo-1h-triazolo[4,5-b]pyridine |
|
102
|
337
|
7ak3A |
Clk1 bound with caf052 |
|
82
|
268
|
6xf0A |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and tiam1 in complex with atp |
|
188
|
639
|
7k7lA |
Structure of a hit for g protein coupled receptor kinase 2 (grk2) inhibitor for the potential treatment of heart failure |
|
83
|
268
|
7kl0A |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b(s1303d) |
|
81
|
280
|
7b30A |
Mst3 in complex with compound g-5555 |
|
80
|
281
|
7b33A |
Mst3 in complex with mria11 |
|
87
|
268
|
6xbpA |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b |
|
81
|
268
|
7kl2A |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b(s1303d) |
|
79
|
308
|
7aqbA |
Crystal structure of human mitogen activated protein kinase 6 (mapk6) |
|
82
|
281
|
7b34A |
Mst3 in complex with compound mria12 |
|
83
|
268
|
6xduA |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b in complex with adp |
|
110
|
334
|
7a4cA |
Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 5,6,7-tribromo-1h-triazolo[4,5-b]pyridine |
|
86
|
268
|
7kl4A |
Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b(s1303d) |
