Found 4011 chains in Genus chains table. Displaying 151 - 200. Applied filters: Proteins

Search results query: Transferase(Phosphotransferase); domain 1

Total Genus Sequence Length pdb Title
69 294 5hniX Crystal structure of cmet wt with compound 3
86 275 5hu9A Crystal structure of abl1 in complex with chmfl-074
118 328 5htcA Crystal structure of haspin (gsg2) in complex with bisubstrate inhibitor arc-3372
91 295 5htiA Crystal structure of c-met kinase domain in complex with lxm108
88 266 5hu3A Drosophila camkii-d136n in complex with a phosphorylated fragment of the eag potassium channel and mg2+/adp
103 351 5hlnA X-ray crystal structure of gsk3b in complex with chir99021
94 363 5hbjA Cdk8-cycc in complex with 8-[2-amino-3-chloro-5-(1-methyl-1h-indazol-5-yl)-pyridin-4-yl]-2,8-diaza-spiro[4.5]decan-1-one
87 299 5hlwA Crystal structure of c-met mutant y1230h in complex with compound 14
117 347 5hd4A Dissecting therapeutic resistance to erk inhibition rat wild type sch772984 in complex with (3r)-1-(2-oxo-2-{4-[4-(pyrimidin-2-yl)phenyl]piperazin-1-yl}ethyl)-n-[3-(pyridin-4-yl)-2h-indazol-5-yl]pyrrolidine-3-carboxamide
75 269 5hieA Braf kinase domain b3ac loop deletion mutant in complex with dabrafenib
81 290 5gzaA Protein o-mannose kinase
78 284 5gz8A Crystal structure of catalytic domain of protein o-mannosyl kinase in ligand-free form
96 305 5fxrA Igfr-1r complex with a pyrimidine inhibitor.
91 294 4usfA Human slk with sb-440719
77 293 4useA Human stk10 (lok) with sb-633825
80 280 4cvaA Mps1 kinase with 3-aminopyridin-2-one inhibitors
96 314 4ckrA Crystal structure of the human ddr1 kinase domain in complex with ddr1-in-1
101 314 4ckjA Crystal structure of ret tyrosine kinase domain bound to adenosine
100 308 4cljA Structure of l1196m mutant 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).
87 324 5canA Egfr kinase domain mutant "tmlr" with compound 27
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
90 324 5c8nA Egfr kinase domain mutant "tmlr" with compound 23
93 275 5cxzA Syk catalytic domain complexed with naphthyridine inhibitor
85 282 5ceoA Dlk in complex with inhibitor 2-((6-(3,3-difluoropyrrolidin-1-yl)-4-(1-(oxetan-3-yl)piperidin-4-yl)pyridin-2-yl)amino)isonicotinonitrile
89 322 5calA Egfr kinase domain mutant "tmlr" with compound 24
92 324 5casA Egfr kinase domain mutant "tmlr" with compound 41a
97 292 5cf8A Crystal structure of janus kinase 2 in complex with n,n-dicyclopropyl-10-ethyl-7-[(3-methoxypropyl)amino] -3-methyl-3,5,8,10-tetraazatricyclo[7.3.0.0,6] dodeca-1(9),2(6),4,7,11-pentaene-11-carboxamide
86 282 5cepA Dlk in complex with inhibitor n-(1-isopropyl-5-(piperidin-4-yl)-1h-pyrazol-3-yl)-4-(trifluoromethyl)pyridin-2-amine
82 349 5dmzA Structure of human bub1 kinase domain phosphorylated at ser969
78 277 5cemA Pseudokinase and c-terminal extension of human tribbles homolog 1
83 323 5caoA Egfr kinase domain mutant "tmlr" with compound 29
99 350 5eknA Crystal structure of mapk13 complex with inhibitor
91 323 5cauA Egfr kinase domain mutant "tmlr" with compound 41b
108 327 5cspA Crystal structure of ck2alpha with compound 5 bound
98 292 5cf5A Crystal structure of janus kinase 2 in complex with n,n-dicyclopropyl-7-[(dimethyl-1,3-thiazol-2-yl)amino]-10-ethyl-3-methyl-3,5,8,10-tetraazatricyclo[7.3.0.02,6] dodeca-1(9),2(6),4,7,11-pentaene-11-carboxamide
67 255 5cekA Pseudokinase domain of human tribbles homolog 1
104 336 5f9eA Structure of protein kinase c theta with compound 10: 2,2-dimethyl-7-(2-oxidanylidene-3~{h}-imidazo[4,5-b]pyridin-1-yl)-1-(phenylmethyl)-3~{h}-quinazolin-4-one
94 322 5caqA Egfr kinase domain mutant "tmlr" with compound 33
91 323 5capA Egfr kinase domain mutant "tmlr" with compound 30
94 309 5fdpA Structure of ddr1 receptor tyrosine kinase in complex with d2099 inhibitor at 2.25 angstroms resolution.
106 327 5cu0A Crystal structure of ck2alpha with 2-hydroxy-5-methylbenzoic acid and n-(3-(3-chloro-4-(phenyl)benzylamino)propyl)acetamide bound
93 289 5cf4A Crystal structure of janus kinase 2 in complex with n,n-dicyclopropyl-10-ethyl-7-[(3-methoxypropyl)amino] -3-methyl-3,5,8,10-tetraazatricyclo[7.3.0.0,6] dodeca-1(9),2(6),4,7,11-pentaene-11-carboxamide
88 324 5cavA Egfr kinase domain with compound 41a
115 350 5bvdA Tetrahydropyrrolo-diazepenones as inhibitors of erk2 kinase
111 348 5buiA Erk2 complexed with 2-pyridiyl tetrahydroazaindazole
91 308 5bvnA Fragment-based discovery of potent and selective ddr1/2 inhibitors
95 322 5c8kA Egfr kinase domain mutant "tmlr" with compound 1
93 274 5c26A Crystal structure of syk in complex with compound 1
92 308 5bvoA Fragment-based discovery of potent and selective ddr1/2 inhibitors
84 273 5c1qB Serine/threonine-protein kinase pim-1