|
91
|
295
|
6drwA |
Jak2 jh1 in complex with jnj-7706621 (crystal form 2) |
|
93
|
290
|
6dbkA |
Tyk2 with compound 8 |
|
95
|
314
|
6d1zA |
Crystal structure of tyrosine-protein kinase receptor in complex with 5-(4-fluorophenyl)thieno[2,3-d]pyrimidin-4(3h)-one inhibitor |
|
93
|
262
|
6cz2A |
Structure of the ptk6 kinase domain |
|
90
|
261
|
6cz4A |
Structure of the ptk6 kinase domain bound to a type ii inhibitor 2-{[(3r,4s)-3-fluoro-1-{[4-(trifluoromethoxy)phenyl]acetyl}piperidin-4-yl]oxy}-5-(1-methyl-1h-imidazol-4-yl)pyridine-3-carboxamide |
|
87
|
262
|
6cz3A |
Structure of the ptk6 kinase domain bound to a type i inhibitor (3-fluoro-4-{[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino}phenyl)(morpholin-4-yl)methanone |
|
97
|
316
|
6d1yA |
Crystal structure of tyrosine-protein kinase receptor in complex with 2,4-dichloro-n-(3-methyl-1-phenyl-1h-pyrazol-5-yl)benzamide inhibitor |
|
86
|
299
|
6d22A |
Crystal structure of tyrosine-protein kinase receptor |
|
93
|
308
|
6cpyA |
Structure of apo grmzm2g135359 pseudokinase |
|
67
|
274
|
6cadA |
Crystal structure of raf kinase domain bound to the inhibitor 2a |
|
73
|
285
|
6c3eA |
Crystal structure of rip1 kinase bound to inhibitor |
|
79
|
286
|
6c7yA |
Crystal structure of inhibitory protein socs1 in complex with jak1 kinase domain |
|
72
|
287
|
6c4dA |
Structure based design of rip1 kinase inhibitors |
|
83
|
272
|
6bs0A |
Jak2 jh2 in complex with 63552444 |
|
74
|
279
|
6bwkA |
Crystal structure of the human mlkl pseudokinase domain t357e/s358e mutant |
|
81
|
270
|
6bl8A |
Predicting the conformational variability of abl tyrosine kinase using molecular dynamics simulations and markov state models |
|
82
|
272
|
6bssA |
Jak2 jh2 in complex with nu6102 |
|
91
|
272
|
6brwA |
Jak2 jh2 in complex with xmu-mp-1 |
|
88
|
288
|
6bbuA |
Crystal structure of jak1 in complex with compound 25 |
|
98
|
289
|
6bbvA |
Crystal structure of jak2 in complex with compound 25 |
|
77
|
282
|
6b5jA |
Tnni3k complexed with a 4,6-diaminopyrimidine |
|
77
|
272
|
6b8uA |
Crystals structure of b-raf kinase domain in complex with an imidazopyridinyl benzamide inhibitor |
|
89
|
264
|
6aubA |
Crystal structure of bruton's tyrosine kinase in complex with inhibitor cgi2815 |
|
78
|
273
|
5zxbA |
Crystal structure of ack1 with compound 10d |
|
72
|
284
|
5zwjA |
Crystal structure of egfr 675-1022 t790m/c797s/v948r in complex with eai045 |
|
93
|
265
|
6auaA |
Crystal structure of bruton's tyrosine kinase in complex with inhibitor cgi2625 |
|
80
|
261
|
5zz4A |
Crystal structure of bruton's tyrosine kinase in complex with inhibitor 2e |
|
90
|
271
|
5zj6A |
Crystal structure of hck kinase complexed with a pyrrolo-pyrimidine inhibitor 7-[trans-4-(4-methylpiperazin-1-yl)cyclohexyl]-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine |
|
96
|
318
|
5yu9A |
Crystal structure of egfr 696-1022 t790m in complex with ibrutinib |
|
88
|
300
|
5zv2A |
Fgfr-1 in complex with ligand lenvatinib |
|
87
|
273
|
5y5tA |
Crystal structures of spleen tyrosine kinase in complex with a novel inhibitor |
|
87
|
289
|
5ya5A |
Crystal structure of c-met in complex with novel inhibitor |
|
88
|
324
|
5y9tA |
Crystal structure of egfr t790m mutant in complex with naquotinib |
|
87
|
271
|
5y5uA |
Crystal structures of spleen tyrosine kinase in complex with a novel inhibitor |
|
84
|
321
|
5y25A |
Egfr kinase domain mutant (t790m/l858r) with covalent ligand ns-062 |
|
98
|
316
|
5x2cA |
Crystal structure of egfr 696-1022 t790m/v948r in complex with sklb(5) |
|
78
|
306
|
5w5oA |
Identification of potent and selective ripk2 inhibitors for the treatment of inflammatory diseases. |
|
88
|
323
|
5xdlA |
Crystal structure of egfr 696-1022 l858r in complex with co-1686 |
|
82
|
274
|
5wijA |
Jak2 pseudokinase in complex with nu6140 |
|
87
|
324
|
5xgmA |
Crystal structure of egfr 696-1022 t790m in complex with go6976 |
|
91
|
312
|
5x2aA |
Crystal structure of egfr 696-1022 t790m/v948r in complex with sklb(3) |
|
87
|
283
|
5wfjA |
The jak3 kinase domain in complex with a covalent inhibitor |
|
73
|
298
|
5xffA |
Crystal structure of ly2874455 in complex of fgfr4 gatekeeper mutation (v550l) |
|
81
|
274
|
5wilA |
Jak2 pseudokinase in complex with azd7762 |
|
70
|
298
|
5xfjA |
Crystal structure of ly2874455 in complex of fgfr4 gatekeeper mutation (v550m) |
|
78
|
274
|
5wikB |
Jak2 pseudokinase in complex with bi-d1870 |
|
94
|
271
|
5vfiA |
Bruton's tyrosine kinase (btk) with gdc-0853 |
|
94
|
290
|
5cf6A |
Crystal structure of janus kinase 2 in complex with n,n-dicyclopropyl-10-[(2s)-2,3-dihydroxypropyl]-3-methyl-7-(methylamino)-3,5,8,10-tetraazatricyclo [7.3.0.02,6]dodeca-1(9),2(6),4,7,11-pentaene-11-carboxamide |
|
87
|
324
|
5canA |
Egfr kinase domain mutant "tmlr" with compound 27 |
|
93
|
275
|
5cxzA |
Syk catalytic domain complexed with naphthyridine inhibitor |
