|
83
|
287
|
4hvdA |
Jak3 kinase domain in complex with 2-cyclopropyl-5h-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((s)-1,2,2-trimethyl-propyl)-amide |
|
91
|
290
|
4f09A |
Discovery and optimization of c-2 methyl imidazo-pyrrolopyridines as potent and orally bioavailable jak1 inhibitors with selectivity over jak2 |
|
98
|
348
|
4ekuA |
Crystal structure of ferm domain of proline-rich tyrosine kinase 2 |
|
93
|
298
|
4e4mA |
Jak2 kinase (jh1 domain) in complex with compound 30 |
|
160
|
403
|
4dylA |
F-bar domain of human fes tyrosine kinase |
|
96
|
298
|
4e6qA |
Jak2 kinase (jh1 domain) triple mutant in complex with compound 12 |
|
101
|
293
|
4e6dA |
Jak2 kinase (jh1 domain) triple mutant in complex with compound 7 |
|
86
|
297
|
4ehzA |
The jak1 kinase domain in complex with inhibitor |
|
88
|
277
|
4ebvA |
Structure of focal adhesion kinase catalytic domain in complex with novel allosteric inhibitor |
|
92
|
290
|
4e4lA |
Jak1 kinase (jh1 domain) in complex with compound 30 |
|
87
|
291
|
4e1zA |
Structure of mouse tyk-2 complexed to a 3-aminoindazole inhibitor |
|
24
|
101
|
4eihA |
Crystal structure of arg sh2 domain |
|
88
|
290
|
4e20A |
Structure of mouse tyk-2 complexed to a 3-aminoindazole inhibitor |
|
107
|
377
|
4e93A |
Crystal structure of human feline sarcoma viral oncogene homologue (v-fes)in complex with tae684 |
|
89
|
302
|
4e4nA |
Jak1 kinase (jh1 domain) in complex with compound 49 |
|
81
|
276
|
4ebwA |
Structure of focal adhesion kinase catalytic domain in complex with novel allosteric inhibitor |
|
13
|
58
|
4eikA |
Crystal structure of the human fyn sh3 domain in complex with the synthetic peptide vsl12 |
|
91
|
302
|
4e5wA |
Jak1 kinase (jh1 domain) in complex with compound 26 |
|
84
|
302
|
4ei4A |
Jak1 kinase (jh1 domain) in complex with compound 20 |
|
82
|
278
|
4dggA |
C-src kinase domain in complex with rm-1-176 |
|
82
|
273
|
4d55A |
Focal adhesion kinase catalytic domain |
|
83
|
272
|
4d4rA |
Focal adhesion kinase catalytic domain |
|
98
|
334
|
4d2vA |
Structure of melk in complex with inhibitors |
|
86
|
272
|
4d5kA |
Focal adhesion kinase catalytic domain |
|
103
|
292
|
4d0wA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
94
|
333
|
4d2tA |
Structure of melk in complex with inhibitors |
|
76
|
265
|
4csvA |
Tyrosine kinase as - a common ancestor of src and abl bound to gleevec |
|
12
|
57
|
4d8dA |
Crystal structure of hiv-1 nef fyn-sh3 r96w variant |
|
103
|
333
|
4d2wA |
Structure of melk in complex with inhibitors |
|
79
|
272
|
4d5hA |
Focal adhesion kinase catalytic domain |
|
98
|
293
|
4d0xA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
81
|
272
|
4d4yA |
Focal adhesion kinase catalytic domain |
|
81
|
273
|
4d58A |
Focal adhesion kinase catalytic domain in complex with bis-anilino pyrimidine inhibitor |
|
94
|
289
|
4d1sA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
103
|
330
|
4cqgA |
The crystal structure of mpk38 in complex with otssp167, an orally- administrative melk selective inhibitor |
|
82
|
272
|
4d4vA |
Focal adhesion kinase catalytic domain |
|
95
|
333
|
4d2pA |
Structure of melk in complex with inhibitors |
|
95
|
330
|
4cyeA |
Crystal structure of avian fak ferm domain fak31-405 at 3.2a |
|
32
|
163
|
4d8kA |
Crystal structure of a sh3-sh2 domains of a lymphocyte-specific protein tyrosine kinase (lck) from homo sapiens at 2.36 a resolution |
|
79
|
272
|
4d4sA |
Focal adhesion kinase catalytic domain |
|
83
|
274
|
4dfnA |
Crystal structure of spleen tyrosine kinase complexed with an adamantylpyrazine inhibitor |
|
87
|
274
|
4dflA |
Crystal structure of spleen tyrosine kinase complexed with a sulfonamidopyrazine piperidine inhibitor |
|
81
|
271
|
4c7tA |
Focal adhesion kinase catalytic domain in complex with a diarylamino- 1,3,5-triazine inhibitor |
|
87
|
309
|
4c8bA |
Structure of the kinase domain of human ripk2 in complex with ponatinib |
|
83
|
261
|
4c3fA |
Structure of lck in complex with a compound discovered by virtual fragment linking |
|
89
|
287
|
4c61A |
Inhibitors of jak2 kinase domain |
|
81
|
272
|
4brxA |
Focal adhesion kinase catalytic domain in complex with a diarylamino- 1,3,5-triazine inhibitor |
|
89
|
287
|
4c62A |
Inhibitors of jak2 kinase domain |
|
104
|
333
|
4bkzA |
Crystal structure of unphosphorylated maternal embryonic leucine zipper kinase (melk) in complex with a benzodipyrazole inhibitor |
|
96
|
291
|
4aqcA |
Triazolopyridine-based inhibitor of janus kinase 2 |
