Found 1565 chains in Genus chains table. Displaying 151 - 200. Applied filters: Proteins

Search results query: Pkinase_Tyr

Total Genus Sequence Length pdb Title
88 325 5j9zA Egfr-t790m in complex with pyrazolopyrimidine inhibitor 1a
78 275 5k9iA Crystal structure of c-src in complex with a covalent lysine probe
107 348 5k5xA Crystal structure of human pdgfra
73 306 5jk3A Crystal structure of tl11-128 bound to tak1-tab1
85 305 5jfxA Crystal structure of trka in complex with pf-06273340
81 301 5jebA Crystal structure of egfr tyrosine kinase domain with novel inhibitor of active state of her2
90 287 5khwA Crystal structure of jak1 in complex with adp
96 295 5k72A Irak4 in complex with compound 21
71 276 5jt2A Brafv600e kinase domain in complex with chemically linked vemurafenib inhibitor vem-bisamide
97 307 5jgaA Crystal structure of human tak1/tab1 fusion protein in complex with ligand 11c
88 306 5jgdA Crystal structure of human tak1/tab1 fusion protein in complex with ligand 12
81 306 5j7bA The identification and pharmacological characterization of 6-(tert-butylsulfonyl)-n-(5-fluoro-1h-indazol-3-yl)quinolin-4-amine (gsk583), a highly potent and selective inhibitor of rip2 kinase, gsk583 complex
90 294 5k76A Irak4 in complex with compound 28
74 288 5k0xA Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor unc2541
77 306 5j7sA Crystal structure of sm1-71 bound to tak1-tab1
83 309 5j79A The identification and pharmacological characterization of 6-(tert-butylsulfonyl)-n-(5-fluoro-1h-indazol-3-yl)quinolin-4-amine (gsk583), a highly potent and selective inhibitor of rip2 kinase, compound 3 complex
78 276 5j5sA Src kinase in complex with a sulfonamide inhibitor
99 312 5iuhA Crystal structure of the anaplastic lymphoma kinase (alk) in complex with 5d
78 271 5itaA Crystal structure of braf kinase domain bound to az-vem
101 312 5iugA Crystal structure of anaplastic lymphoma kinase (alk) in complex with 5a
84 292 5imxA Anaplastic lymphoma kinase (alk) catalytic domain complexed with novel inhibitor 3-sulfonylpyrazol-4-amino pyrimidine
82 286 5ia0A Crystal structure of ephrin a2 (epha2) receptor protein kinase with alisertib (mln8237)
91 291 5ia2A Crystal structure of ephrin a2 (epha2) receptor protein kinase with compound 66
82 293 5i9zA Crystal structure of ephrin a2 (epha2) receptor protein kinase with danusertib (pha739358)
83 291 5i9wA Crystal structure of ephrin a2 (epha2) receptor protein kinase with anp
81 284 5ia1A Crystal structure of ephrin a2 (epha2) receptor protein kinase with mln8054
87 292 5i9vA Crystal structure of ephrin a2 (epha2) receptor protein kinase with ags
90 297 5i9yA Crystal structure of ephrin a2 (epha2) receptor protein kinase with dasatinib
84 291 5i8aA Trka with (6~{r})-3-methylsulfanyl-6-phenyl-1-(1~{h}-pyrazol-3-yl)-6,7-dihydro-5~{h}-thieno[3,4-c]pyridin-4-one
80 295 5ia3A Crystal structure of ephrin a2 (epha2) receptor protein kinase with pd173955
83 273 5ia4A Crystal structure of ephrin a2 (epha2) receptor protein kinase with foretinib (xl880)
91 293 5i9xA Crystal structure of ephrin a2 (epha2) receptor protein kinase with bosutinib (ski-606)
93 304 5hznA Structure of nvp-aew541 in complex with igf-1r kinase
128 447 5h0gA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor (s)-2-(((1r,4s)-4-(4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)amino)-n,4-dimethylpentanamide
87 284 5i4nA Crystal structure of the e596a v617f mutant jak2 pseudokinase domain bound to mg-atp
75 285 5hx6A Crystal structure of rip1 kinase with a benzo[b][1,4]oxazepin-4-one
72 311 5hvkA Crystal structure of limk1 mutant d460n in complex with full-length cofilin-1
89 300 5hx8A Jak1 complex with 4-[(4-aminocyclohexyl)amino]-3-(1h-benzimidazol-2-yl)-1h-pyridin-2-one
86 275 5hu9A Crystal structure of abl1 in complex with chmfl-074
80 293 5horA Crystal structure of c-met-m1250t in complex with sar125844.
69 294 5hniX Crystal structure of cmet wt with compound 3
91 295 5htiA Crystal structure of c-met kinase domain in complex with lxm108
87 299 5hlwA Crystal structure of c-met mutant y1230h in complex with compound 14
75 269 5hieA Braf kinase domain b3ac loop deletion mutant in complex with dabrafenib
78 284 5gz8A Crystal structure of catalytic domain of protein o-mannosyl kinase in ligand-free form
125 447 5h0eA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor (s)-2-(((1r,4s)-4-(4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)amino)-4-methylpentanamide
94 303 5grnA Crystal structure of pdgfra in complex with wq-c-159
81 290 5gzaA Protein o-mannose kinase
96 305 5fxrA Igfr-1r complex with a pyrimidine inhibitor.
101 314 4ckjA Crystal structure of ret tyrosine kinase domain bound to adenosine