|
88
|
343
|
3zh8A |
A novel small molecule apkc inhibitor |
|
78
|
283
|
3zfxA |
Crystal structure of ephb1 |
|
90
|
296
|
3zbfA |
Structure of human ros1 kinase domain in complex with crizotinib |
|
73
|
279
|
3wzjA |
Crystal structure of human mps1 catalytic domain in complex with 4-(6-(cyclohexylamino)-8-(((tetrahydro-2h-pyran-4-yl)methyl)amino)imidazo[1,2-b]pyridazin-3-yl)-n-cyclopropylbenzamide |
|
118
|
334
|
3wowA |
Crystal structure of human ck2a with amppnp |
|
84
|
290
|
3wf6A |
Crystal structure of s6k1 kinase domain in complex with a pyrazolopyrimidine derivative 4-[4-(1h-indol-3-yl)-3,6-dihydropyridin-1(2h)-yl]-1h-pyrazolo[3,4-d]pyrimidine |
|
101
|
344
|
3zlxA |
Crystal structure of mek1 in complex with fragment 18 |
|
94
|
344
|
3w8qA |
Structure of the human mitogen-activated protein kinase kinase 1 (mek1) |
|
84
|
285
|
3zepA |
Crystal structure of jak3 kinase domain in complex with a pyrrolopyrazine-2-phenyl ether inhibitor |
|
85
|
288
|
3wigA |
Human mek1 kinase in complex with ch5126766 and mgamp-pnp |
|
90
|
290
|
3we4A |
Crystal structure of s6k1 kinase domain in complex with a pyrimidine derivative pf-4708671 2-{[4-(5-ethylpyrimidin-4-yl)piperazin-1-yl]methyl}-5-(trifluoromethyl)-1h-benzimidazole |
|
97
|
343
|
3zm4A |
Crystal structure of mek1 in complex with fragment 1 |
|
121
|
334
|
3warA |
Crystal structure of human ck2a |
|
88
|
286
|
3zbxA |
X-ray structure of c-met kinase in complex with inhibitor 6-((6-(4- fluorophenyl)-(1,2,4)triazolo(4,3-b)(1,2,4)triazin-3-yl)methyl) quinoline. |
|
89
|
309
|
3zduA |
Crystal structure of the human cdkl3 kinase domain |
|
85
|
273
|
3we8A |
Pim-1 kinase in complex with ruthenium-based inhibitor |
|
74
|
275
|
3zhpC |
Human mst3 (stk24) in complex with mo25beta |
|
99
|
349
|
3zdiA |
Glycogen synthase kinase 3 beta complexed with axin peptide and inhibitor 7d |
|
76
|
280
|
3zewA |
Crystal structure of ephb4 in complex with staurosporine |
|
78
|
279
|
3zfmA |
Crystal structure of ephb2 |
|
93
|
293
|
3zclA |
X-ray structure of c-met kinase in complex with inhibitor (s)-3-(1-(1h-pyrrolo(2,3-b)pyridin-3-yl)ethyl)-n-isopropyl-(1,2,4)triazolo(4,3- b)pyridazin-6-amine |
|
72
|
280
|
3wyyA |
Crystal structure of human mps1 catalytic domain in complex with (e)-3-(4-((6-(((3s,5s,7s)-adamantan-1-yl)amino)-4-amino-5-cyanopyridin-2-yl)amino)-2-(cyanomethoxy)phenyl)-n-(2-methoxyethyl)acrylamide |
|
89
|
288
|
3wf8A |
Crystal structure of s6k1 kinase domain in complex with a quinoline derivative 2-oxo-2-[(4-sulfamoylphenyl)amino]ethyl 7,8,9,10-tetrahydro-6h-cyclohepta[b]quinoline-11-carboxylate |
|
104
|
344
|
3zlsA |
Crystal structure of mek1 in complex with fragment 6 |
|
90
|
322
|
3vvhA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in complex with an inhibitor and mgatp |
|
99
|
317
|
3w32A |
Egfr kinase domain complexed with compound 20a |
|
92
|
320
|
3w2rA |
Egfr kinase domain t790m/l858r mutant with compound 4 |
|
92
|
298
|
3w0sA |
Crystal structure of aminoglycoside phosphotransferase aph(4)-ia, ternary complex with amp-pnp and hygromycin b |
|
83
|
269
|
3vw6A |
Crystal structure of human apoptosis signal-regulating kinase 1 (ask1) with imidazopyridine inhibitor |
|
110
|
358
|
3vuiA |
Crystal structure of a cysteine-deficient mutant m2 in map kinase jnk1 |
|
92
|
319
|
3w2sA |
Egfr kinase domain with compound4 |
|
97
|
321
|
3w2qA |
Egfr kinase domain t790m/l858r mutant with hki-272 |
|
94
|
318
|
3w33A |
Egfr kinase domain complexed with compound 19b |
|
78
|
263
|
3w10A |
Aurora kinase a complexed to pyrazole aminoquinoline i |
|
70
|
280
|
3w1fA |
Crystal structure of human mps1 catalytic domain in complex with 5-(5-ethoxy-6-(1-methyl-1h-pyrazol-4-yl)-1h-indazol-3-yl)-2-methylbenzenesulfonamide |
|
90
|
296
|
3w0qA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia (n203a), ternary complex with amp-pnp and hygromycin b |
|
187
|
540
|
3vwaA |
Crystal structure of cex1p |
|
84
|
295
|
3w0pA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia (d198a), ternary complex with adp and hygromycin b |
|
95
|
321
|
3w2oA |
Egfr kinase domain t790m/l858r mutant with tak-285 |
|
71
|
263
|
3w16A |
Structure of aurora kinase a complexed to pyrazole-aminoquinoline inhibitor iii |
|
88
|
295
|
3w0oA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia, ternary complex with adp and hygromycin b |
|
67
|
263
|
3w18A |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xiii |
|
86
|
347
|
3w55A |
The structure of erk2 in complex with fr148083 |
|
89
|
295
|
3w0rA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia (n202a), ternary complex with amp-pnp and hygromycin b |
|
92
|
293
|
3w0mA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia, apo form |
|
117
|
447
|
3vs6A |
Crystal structure of hck complexed with a pyrazolo-pyrimidine inhibitor tert-butyl {4-[4-amino-1-(propan-2-yl)-1h-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}carbamate |
|
52
|
261
|
3w2cA |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xv |
|
87
|
295
|
3w0nA |
Crystal structure of a thermostable mutant of aminoglycoside phosphotransferase aph(4)-ia, ternary complex with amp-pnp and hygromycin b |
|
94
|
328
|
3vw8A |
Crystal structure of human c-met kinase domain with its inhibitor |
|
98
|
361
|
3vumA |
Crystal structure of a cysteine-deficient mutant m7 in map kinase jnk1 |
