|
72
|
263
|
4byiA |
Aurora a kinase bound to a highly selective imidazopyridine inhibitor |
|
105
|
544
|
4cfeA |
Structure of full length human ampk in complex with a small molecule activator, a benzimidazole derivative (991) |
|
93
|
290
|
4btkA |
Ttbk1 in complex with inhibitor |
|
101
|
544
|
4cffA |
Structure of full length human ampk in complex with a small molecule activator, a thienopyridone derivative (a-769662) |
|
87
|
309
|
4c8bA |
Structure of the kinase domain of human ripk2 in complex with ponatinib |
|
77
|
264
|
4c3pA |
Structure of dephosphorylated aurora a (122-403) bound to tpx2 and amppcp |
|
69
|
291
|
4c0tA |
Candida albicans pkh kinase domain |
|
95
|
292
|
4btjA |
Ttbk1 in complex with atp |
|
77
|
262
|
4c3rA |
Structure of dephosphorylated aurora a (122-403) bound to amppcp |
|
93
|
292
|
4btmA |
Ttbk1 in complex with inhibitor |
|
82
|
320
|
4cc9A |
Crystal structure of human samhd1 (amino acid residues 582-626) bound to vpx isolated from sooty mangabey and human dcaf1 (amino acid residues 1058-1396) |
|
19
|
97
|
4c4kT |
Crystal structure of the titin m10-obscurin ig domain 1 complex |
|
89
|
271
|
4c2vA |
Aurora b kinase in complex with the specific inhibitor barasertib |
|
269
|
945
|
4anxA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
95
|
310
|
4c57A |
Structure of gak kinase in complex with a nanobody |
|
89
|
269
|
4c2wA |
Crystal structure of aurora b in complex with amp-pnp |
|
82
|
273
|
4bzoA |
Crystal structure of pim1 in complex with a pyrrolo-pyrazinone inhibitor |
|
83
|
273
|
4bznA |
Crystal structure of pim1 in complex with a pyrrolo(1,2-a)pyrazinone inhibitor |
|
87
|
265
|
4cegA |
Crystal structure of aurora a 122-403 c290a, c393a bound to adp |
|
70
|
307
|
4c59A |
Structure of gak kinase in complex with nanobody (nbgak_4) |
|
16
|
94
|
4c4kO |
Crystal structure of the titin m10-obscurin ig domain 1 complex |
|
71
|
263
|
4byjA |
Aurora a kinase bound to a highly selective imidazopyridine inhibitor |
|
7
|
21
|
4cfhC |
Structure of an active form of mammalian ampk |
|
75
|
307
|
4c58A |
Structure of gak kinase in complex with nanobody (nbgak_4) |
|
277
|
1057
|
4a55A |
Crystal structure of p110alpha in complex with ish2 of p85alpha and the inhibitor pik-108 |
|
92
|
461
|
4cfhA |
Structure of an active form of mammalian ampk |
|
88
|
304
|
4bddA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
99
|
303
|
4b9dA |
Crystal structure of human nima-related kinase 1 (nek1) with inhibitor. |
|
206
|
952
|
4aofA |
Selective small molecule inhibitor discovered by chemoproteomic assay platform reveals regulation of th17 cell differentiation by pi3kgamma |
|
104
|
333
|
4bkzA |
Crystal structure of unphosphorylated maternal embryonic leucine zipper kinase (melk) in complex with a benzodipyrazole inhibitor |
|
82
|
263
|
4bn1A |
Crystal structure of v174m mutant of aurora-a kinase |
|
82
|
303
|
4bdcA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
89
|
271
|
4b8mA |
Aurora b kinase in complex with vx-680 |
|
99
|
299
|
4b4lA |
Crystal structure of an ard dap-kinase 1 mutant |
|
256
|
945
|
4anwA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
249
|
945
|
4anuA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
274
|
949
|
3zvvA |
Fragment bound to pi3kinase gamma |
|
80
|
273
|
4as0A |
Cyclometalated phthalimides as protein kinase inhibitors |
|
102
|
332
|
4bl1A |
Crystal structure of unphosphorylated maternal embryonic leucine zipper kinase (melk) in complex with amp-pnp |
|
85
|
303
|
4bdkA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
80
|
304
|
4bdbA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
74
|
265
|
4b8lA |
Aurora b kinase p353g mutant |
|
280
|
940
|
3zimA |
Discovery of a potent and isoform-selective targeted covalent inhibitor of the lipid kinase pi3kalpha |
|
87
|
290
|
4au8A |
Crystal structure of compound 4a in complex with cdk5, showing an unusual binding mode to the hinge region via a water molecule |
|
87
|
304
|
4bdfA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
249
|
946
|
4anvA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
85
|
307
|
4bdiA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
85
|
303
|
4bdjA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
78
|
293
|
4bc6A |
Crystal structure of human serine threonine kinase-10 bound to novel bosutinib isoform 1, previously thought to be bosutinib |
|
95
|
350
|
4b7tA |
Glycogen synthase kinase 3 beta complexed with axin peptide and leucettine l4 |
