|
80
|
304
|
4bdbA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
82
|
279
|
4bi0A |
Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor |
|
9
|
94
|
4bjjB |
Sfc1-sfc7 dimerization module |
|
104
|
311
|
4asxA |
Crystal structure of activin receptor type-iia (acvr2a) kinase domain in complex with dihydro-bauerine c |
|
89
|
271
|
4b8mA |
Aurora b kinase in complex with vx-680 |
|
127
|
409
|
4azfA |
Human dyrk2 in complex with leucettine l41 |
|
96
|
314
|
4bkjA |
Crystal structure of the human ddr1 kinase domain in complex with imatinib |
|
91
|
288
|
4bbfA |
Aminoalkylpyrimidine inhibitor complexes with jak2 |
|
83
|
288
|
4bbeA |
Aminoalkylpyrimidine inhibitor complexes with jak2 |
|
87
|
299
|
4bcmA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
100
|
316
|
4bbmA |
Crystal structure of the human cdkl2 kinase domain with bound tcs 2312 |
|
82
|
263
|
4bn1A |
Crystal structure of v174m mutant of aurora-a kinase |
|
96
|
291
|
4aqcA |
Triazolopyridine-based inhibitor of janus kinase 2 |
|
88
|
299
|
4bcoA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
82
|
279
|
4bi1A |
Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor |
|
97
|
299
|
4at4A |
Crystal structure of trkb kinase domain in complex with ex429 |
|
79
|
283
|
4bb4A |
Ephb4 kinase domain inhibitor complex |
|
74
|
265
|
4b8lA |
Aurora b kinase p353g mutant |
|
76
|
298
|
4bcqA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
146
|
468
|
4aztA |
Co-crystal structure of wbdd and kinase inhibitor ly294002. |
|
82
|
322
|
4bciA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
139
|
416
|
4aw2A |
Crystal structure of cdc42 binding protein kinase alpha (mrck alpha) |
|
85
|
303
|
4bdjA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
110
|
357
|
4awiA |
Human jnk1alpha kinase with 4-phenyl-7-azaindole ikk2 inhibitor. |
|
86
|
304
|
4bdaA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
148
|
470
|
4azvA |
Co-crystal structure of wbdd and kinase inhibitor gw435821x. |
|
85
|
307
|
4bdiA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
141
|
434
|
4axdA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with amppnp |
|
77
|
293
|
4aw1A |
Human pdk1 kinase domain in complex with allosteric compound ps210 bound to the pif-pocket |
|
97
|
299
|
4at3A |
Crystal structure of trkb kinase domain in complex with cpd5n |
|
100
|
347
|
4b99A |
Crystal structure of mapk7 (erk5) with inhibitor |
|
95
|
350
|
4b7tA |
Glycogen synthase kinase 3 beta complexed with axin peptide and leucettine l4 |
|
84
|
321
|
4bchA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
141
|
445
|
4azwA |
Crystal structure of monomeric wbdd. |
|
134
|
435
|
4axfA |
Insp5 2-k in complex with ins(3,4,5,6)p4 plus amppnp |
|
89
|
304
|
4bdgA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
99
|
299
|
4at5A |
Crystal structure of trkb kinase domain in complex with gw2580 |
|
78
|
293
|
4bc6A |
Crystal structure of human serine threonine kinase-10 bound to novel bosutinib isoform 1, previously thought to be bosutinib |
|
87
|
299
|
4bcpA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
135
|
434
|
4axeA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with adp |
|
91
|
296
|
4bggA |
Crystal structure of the acvr1 kinase in complex with ldn-213844 |
|
152
|
470
|
4azsA |
High resolution (2.2 a) crystal structure of wbdd. |
|
87
|
303
|
4bdhA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
89
|
304
|
4bdeA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
79
|
285
|
4aw0A |
Human pdk1 kinase domain in complex with allosteric compound ps182 bound to the pif-pocket |
|
83
|
321
|
4bcjA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
78
|
291
|
4auaA |
Liganded x-ray crystal structure of cyclin dependent kinase 6 (cdk6) |
|
84
|
271
|
4bicA |
Crystal structures of ask1-inhibitor complexes |
|
127
|
437
|
4aqkA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with adp and ip6 |
|
81
|
271
|
4bhnA |
Crystal structures of ask1-inhibitor complexes |
