|
105
|
401
|
3p23A |
Crystal structure of the human kinase and rnase domains in complex with adp |
|
111
|
328
|
3owjA |
Human ck2 catalytic domain in complex with a pyridocarbazole derivative inhibitor |
|
114
|
325
|
3ofmA |
Structure of a human ck2alpha prime, the paralog isoform of the catalytic subunit of protein kinase ck2 from homo sapiens |
|
106
|
330
|
3owkA |
Human ck2 catalytic domain in complex with a benzopyridoindole derivative inhibitor |
|
85
|
283
|
3otuA |
Pdk1 mutant bound to allosteric disulfide fragment activator js30 |
|
31
|
119
|
3ostA |
Structure of the kinase associated-1 (ka1) from kcc4p |
|
81
|
267
|
3ot3A |
X-ray crystal structure of compound 22k bound to human chk1 kinase domain |
|
32
|
119
|
3osmA |
Structure of the kinase associated domain-1 (ka1) from kcc4p |
|
73
|
272
|
3og7A |
B-raf kinase v600e oncogenic mutant in complex with plx4032 |
|
85
|
281
|
3oriA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 1) |
|
106
|
321
|
3op5A |
Human vaccinia-related kinase 1 |
|
89
|
286
|
3orzA |
Pdk1 mutant bound to allosteric disulfide fragment activator 2a2 |
|
27
|
100
|
3oseA |
Structure of the kinase associated domain 1 (ka1) from mark1 kinase |
|
268
|
947
|
3nzuA |
Structure-based optimization of pyrazolo -pyrimidine and -pyridine inhibitors of pi3-kinase |
|
85
|
287
|
3p1aA |
Structure of human membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase myt1 (pkmyt1) |
|
81
|
280
|
3oroA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 4) |
|
68
|
263
|
3o51A |
Crystal structure of anthranilamide 10 bound to auroraa |
|
17
|
83
|
3ny5A |
Crystal structure of the rbd domain of serine/threonine-protein kinase b-raf from homo sapiens. northeast structural genomics consortium target hr4694f |
|
82
|
289
|
3o0gA |
Crystal structure of cdk5:p25 in complex with an atp analogue |
|
70
|
263
|
3o50A |
Crystal structure of benzamide 9 bound to auroraa |
|
96
|
335
|
3ocbA |
Akt1 kinase domain with pyrrolopyrimidine inhibitor |
|
66
|
152
|
3o0zA |
Crystal structure of a coiled-coil domain from human rock i |
|
99
|
428
|
3o96A |
Crystal structure of human akt1 with an allosteric inhibitor |
|
119
|
331
|
3ngaA |
Human ck2 catalytic domain in complex with cx-4945 |
|
88
|
286
|
3nuyA |
Phosphoinositide-dependent kinase-1 (pdk1) with fragment17 |
|
80
|
263
|
3nrmA |
Imidazo[1,2-a]pyrazine-based aurora kinase inhibitors |
|
84
|
288
|
3nunA |
Phosphoinositide-dependent kinase-1 (pdk1) with lead compound |
|
81
|
266
|
3nlbA |
Novel kinase profile highlights the temporal basis of context dependent checkpoint pathways to cell death |
|
85
|
286
|
3nuuA |
Phosphoinositide-dependent kinase-1 (pdk1) with fragment11 |
|
85
|
286
|
3nusA |
Phosphoinositide-dependent kinase-1 (pdk1) with fragment8 |
|
114
|
327
|
3nszA |
Human ck2 catalytic domain in complex with amppn |
|
260
|
950
|
3ml8A |
Discovery of the highly potent pi3k/mtor dual inhibitor pf-04691502 through structure based drug design |
|
85
|
287
|
3nayA |
Pdk1 in complex with inhibitor mp6 |
|
278
|
950
|
3ml9A |
Discovery of the highly potent pi3k/mtor dual inhibitor pf-04691502 through structure based drug design |
|
77
|
285
|
3naxA |
Pdk1 in complex with inhibitor mp7 |
|
113
|
399
|
3nczA |
X-ray co-structure of rho-associated protein kinase (rock1) with a potent 2h-isoquinolin-1-one inhibitor |
|
108
|
398
|
3ndmA |
Crystal structure of rho-associated protein kinase (rock1) with a potent isoquinolone derivative |
|
99
|
332
|
3mvhA |
Crystal structure of akt-1-inhibitor complexes |
|
81
|
263
|
3mygA |
Aurora a kinase complexed with sch 1473759 |
|
70
|
271
|
3mn3A |
An inhibited conformation for the protein kinase domain of the saccharomyces cerevisiae ampk homolog snf1 |
|
0
|
10
|
3mv5C |
Crystal structure of akt-1-inhibitor complexes |
|
94
|
334
|
3mv5A |
Crystal structure of akt-1-inhibitor complexes |
|
239
|
947
|
3mjwA |
Pi3 kinase gamma with a benzofuranone inhibitor |
|
27
|
107
|
3mopG |
The ternary death domain complex of myd88, irak4, and irak2 |
|
98
|
303
|
3mfsA |
Cask-4m cam kinase domain, amppnp |
|
94
|
351
|
3m1sA |
Structure of ruthenium half-sandwich complex bound to glycogen synthase kinase 3 |
|
93
|
297
|
3m42A |
Crystal structure of mapkap kinase 2 (mk2) complexed with a tetracyclic atp site inhibitor |
|
101
|
302
|
3mfrA |
Cask-4m cam kinase domain, native |
|
263
|
948
|
3lj3A |
Pi3-kinase-gamma with a pyrrolopyridine-benzofuran inhibitor |
|
111
|
329
|
3mb6A |
Human ck2 catalytic domain in complex with a difurane derivative inhibitor (cpa) |
