|
66
|
264
|
3v5jA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 090 |
|
104
|
349
|
3uvqA |
Human p38 map kinase in complex with a dibenzosuberone derivative |
|
103
|
359
|
3vheA |
Crystal structure of human vegfr2 kinase domain with a novel pyrrolopyrimidine inhibitor. |
|
81
|
271
|
3vbvA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
65
|
265
|
3v8wA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 469 |
|
90
|
290
|
3uytA |
Crystal structure of ck1d with pf670462 from p1 crystal form |
|
81
|
271
|
3vbtA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
83
|
291
|
3uysA |
Crystal structure of apo human ck1d |
|
70
|
264
|
3up7A |
Aurora a in complex with yl1-038-09 |
|
67
|
264
|
3uohA |
Aurora a in complex with rpm1722 |
|
85
|
353
|
3uibA |
Map kinase lmampk10 from leishmania major in complex with sb203580 |
|
59
|
288
|
3uiuA |
Crystal structure of apo-pkr kinase domain |
|
87
|
266
|
3uodA |
Aurora a in complex with rpm1693 |
|
95
|
287
|
3ugcA |
Structural basis of jak2 inhibition by the type ii inhibtor nvp-bbt594 |
|
89
|
309
|
3uc3A |
The crystal structure of snf1-related kinase 2.3 |
|
71
|
264
|
3uo6A |
Aurora a in complex with yl5-083 |
|
85
|
276
|
3uqgA |
C-src kinase domain in complex with bumpless bki analog uw1243 |
|
86
|
322
|
3ug1A |
Crystal structure of the mutated egfr kinase domain (g719s/t790m) in the apo form |
|
122
|
431
|
3udtA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with adp and ip5. |
|
103
|
329
|
3u87A |
Structure of a chimeric construct of human ck2alpha and human ck2alpha' in complex with a non-hydrolysable atp-analogue |
|
73
|
265
|
3uokA |
Aurora a in complex with yl5-81-1 |
|
78
|
298
|
3uliA |
Human cyclin dependent kinase 2 (cdk2) bound to azabenzimidazole derivative |
|
79
|
270
|
3ue4A |
Structural and spectroscopic analysis of the kinase inhibitor bosutinib binding to the abl tyrosine kinase domain |
|
78
|
269
|
3uixA |
Crystal structure of pim1 kinase in complex with small molecule inhibitor |
|
77
|
302
|
3uimA |
Structural basis for the impact of phosphorylation on plant receptor-like kinase bak1 activation |
|
82
|
307
|
3uc4A |
The crystal structure of snf1-related kinase 2.6 |
|
79
|
299
|
3ujgA |
Crystal structure of snrk2.6 in complex with hab1 |
|
103
|
331
|
3u9cA |
Structure of a c-terminal deletion mutant of human protein kinase ck2 catalytic subunit with the atp-competitive inhibitor resorufin |
|
87
|
298
|
3ubdA |
Structure of n-terminal domain of rsk2 kinase in complex with flavonoid glycoside sl0101 |
|
153
|
464
|
3upxA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1300 |
|
71
|
263
|
3unzA |
Aurora a in complex with rpm1679 |
|
82
|
268
|
3umxA |
Crystal structure of pim1 kinase in complex with inhibitor (z)-2-[(1h-indol-3-yl)methylene]-7-(azepan-1-ylmethyl)-6-hydroxybenzofuran-3(2h)-one |
|
107
|
433
|
3udsA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with adp. |
|
75
|
263
|
3uolA |
Aurora a in complex with so2-162 |
|
81
|
268
|
3umwA |
Crystal structure of pim1 kinase in complex with inhibitor (z)-2-[(1h-indazol-3-yl)methylene]-6-methoxy-7-(piperazin-1-ylmethyl)benzofuran-3(2h)-one |
|
79
|
306
|
3udbA |
Crystal structure of snrk2.6 |
|
81
|
266
|
3up2A |
Aurora a in complex with rpm1686 |
|
84
|
298
|
3unjA |
Cdk2 in complex with inhibitor yl1-038-31 |
|
122
|
434
|
3udzA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with adp and ip6. |
|
92
|
297
|
3tzmA |
Tgf-beta receptor type 1 in complex with sb431542 |
|
116
|
347
|
3uvrA |
Human p38 map kinase in complex with km064 |
|
95
|
322
|
3ug2A |
Crystal structure of the mutated egfr kinase domain (g719s/t790m) in complex with gefitinib |
|
78
|
266
|
3uo4A |
Aurora a in complex with rpm1680 |
|
77
|
302
|
3ulzA |
Crystal structure of apo bak1 |
|
111
|
349
|
3u8wA |
Crystal structure of p38a mitogen-activated protein kinase in complex with a triazolopyridazinone inhibitor |
|
81
|
277
|
3tz7A |
Kinase domain of csrc in complex with rl103 |
|
76
|
277
|
3tz9A |
Kinase domain of csrc in complex with rl130 |
|
79
|
265
|
3u9nA |
X-ray crystal structure of compound 1 bound to human chk1 kinase domain |
|
92
|
275
|
3u4wA |
Src in complex with dna-templated macrocyclic inhibitor mc4b |
|
89
|
296
|
3tykA |
Crystal structure of aminoglycoside phosphotransferase aph(4)-ia |
