Found 1502 chains in Genus chains table. Displaying 701 - 750. Applied filters: Proteins

Search results query ec: 2.7.10.1

Total Genus Sequence Length pdb Title
91 310 4dceA Crystal structure of human anaplastic lymphoma kinase in complex with a piperidine-carboxamide inhibitor
13 107 4crpA Solution structure of a trkaig2 domain construct for use in drug discovery
87 295 4degA Crystal structure of c-met in complex with triazolopyridazine inhibitor 2
95 302 4d2rA Human igf in complex with a dyrk1b inhibitor
95 308 4cmtA Structure of the human anaplastic lymphoma kinase in complex with the inhibitor 3-((1r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2-yl)phenyl)ethoxy)- 5-(3-(methylsulfonyl)phenyl)pyridin-2-amine
98 308 4cd0A Structure of l1196m mutant human anaplastic lymphoma kinase in complex with 2-(5-(6-amino-5-((r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2- yl)phenyl)ethoxy)pyridin-3-yl)-4-methylthiazol-2-yl)propane-1,2-diol
94 308 4cnhA Structure of the human anaplastic lymphoma kinase in complex with the inhibitor 3-((1r)-1-(5-fluoro-2-methoxyphenyl)ethoxy)-5-(1-methyl-1h- 1,2,3-triazol-5-yl)pyridin-2-amine
96 308 4cmuA Structure of the human anaplastic lymphoma kinase in complex with the inhibitor (10r)-7-amino-12-fluoro-1,3,10,16-tetramethyl-16,17-dihydro- 1h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11)benzoxadiazacyclotetradecin-15(10h)-one
98 308 4cliA Structure of the human anaplastic lymphoma kinase in complex with pf- 06463922 ((10r)-7-amino-12-fluoro-2,10,16-trimethyl-15-oxo-10,15,16, 17-tetrahydro-2h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecine-3-carbonitrile).
12 197 4bskA Crystal structure of vegf-c in complex with vegfr-3 domains d1-2
96 309 4cmoA Structure of the human anaplastic lymphoma kinase in complex with the inhibitor 2-((1r)-1-((3-amino-6-(2-methoxypyridin-3-yl)pyrazin-2-yl) oxy)ethyl)-4-fluoro-n-methylbenzamide
95 314 4ckiA Crystal structure of oncogenic ret tyrosine kinase m918t bound to adenosine
93 308 4ccbA Structure of the human anaplastic lymphoma kinase in complex with 3-((r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2-yl)phenyl)ethoxy)-5-(5-methyl-1h- pyrazol-4-yl)pyridin-2-amine
41 227 4bsjA Crystal structure of vegfr-3 extracellular domains d4-5
96 309 4ccuA Structure of the human anaplastic lymphoma kinase in complex with 2-(5-(6-amino-5-((r)-1-(5-fluoro-2-(2h-1,2,3-triazol-2-yl)phenyl)ethoxy) pyridin-3-yl)-4-methylthiazol-2-yl)propan-2-ol
97 299 4at4A Crystal structure of trkb kinase domain in complex with ex429
102 312 4asdA Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sorafenib (bay 43-9006)
96 314 4bkjA Crystal structure of the human ddr1 kinase domain in complex with imatinib
79 283 4bb4A Ephb4 kinase domain inhibitor complex
63 505 4bkfA Crystal structure of the human epha4 ectodomain in complex with human ephrinb3
47 514 4bk4A Crystal structure of the human epha4 ectodomain
76 282 4aw5A Complex of the ephb4 kinase domain with an oxindole inhibitor
58 507 4bkaA Crystal structure of the human epha4 ectodomain in complex with human ephrin a5
58 507 4bk5A Crystal structure of the human epha4 ectodomain in complex with human ephrin a5 (amine-methylated sample)
97 299 4at3A Crystal structure of trkb kinase domain in complex with cpd5n
99 299 4at5A Crystal structure of trkb kinase domain in complex with gw2580
95 299 4aszA Crystal structure of apo trkb kinase domain
89 317 4agdA Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sunitinib (su11248) (n-2-diethylaminoethyl)-5-((z)-(5- fluoro-2-oxo-1h-indol-3-ylidene)methyl)-2,4-dimethyl-1h-pyrrole-3- carboxamide)
93 286 3zzeA Crystal structure of c-met kinase domain in complex with n'-((3z)-4- chloro-7-methyl-2-oxo-1,2-dihydro-3h-indol-3-ylidene)-2-(4- hydroxyphenyl)propanohydrazide
81 340 4ag4A Crystal structure of a ddr1-fab complex
96 308 4anlA Structure of g1269a mutant anaplastic lymphoma kinase
95 293 3zxzA X-ray structure of pf-04217903 bound to the kinase domain of c-met
100 318 4agcA Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with axitinib (ag-013736) (n-methyl-2-(3-((e)-2-pyridin-2-yl- vinyl)-1h-indazol-6-ylsulfanyl)-benzamide)
98 312 3zosA Structure of the ddr1 kinase domain in complex with ponatinib
98 309 4anqA Structure of g1269a mutant anaplastic lymphoma kinase in complex with crizotinib
103 312 4aseA Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with tivozanib (av-951)
91 293 4aoiA Crystal structure of c-met kinase domain in complex with 4-(3-((1h- pyrrolo(2,3-b)pyridin-3-yl)methyl)-(1,2,4)triazolo(4,3-b)(1,2,4) triazin-6-yl)benzonitrile
100 303 4ag8A Crystal structure of the vegfr2 kinase domain in complex with axitinib (ag-013736) (n-methyl-2-(3-((e)-2-pyridin-2-yl-vinyl)-1h- indazol-6-ylsulfanyl)-benzamide)
91 293 4ap7A Crystal structure of c-met kinase domain in complex with 4-((6-(4- fluorophenyl)-(1,2,4)triazolo(4,3-b)(1,2,4)triazin-3-yl)methyl)phenol
85 285 3zzwA Crystal structure of the kinase domain of ror2
96 309 4ansA Structure of l1196m,g1269a double mutant anaplastic lymphoma kinase in complex with crizotinib
84 290 4aojA Human trka in complex with the inhibitor az-23
97 303 3wzeA Kdr in complex with ligand sorafenib
78 283 3zfxA Crystal structure of ephb1
82 274 3zfyA Crystal structure of ephb3
91 293 3zc5A X-ray structure of c-met kinase in complex with inhibitor (s)-6-(1-(6- (1-methyl-1h-pyrazol-4-yl)-(1,2,4)triazolo(4,3-b)pyridazin-3-yl)ethyl) quinoline.
94 298 3wzdA Kdr in complex with ligand lenvatinib
90 296 3zbfA Structure of human ros1 kinase domain in complex with crizotinib
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