Found 3795 chains in Genus chains table. Displaying 151 - 200. Applied filters: Proteins

Search results query: Pkinase

Total Genus Sequence Length pdb Title
195 639 7k7zA Structure of a hit for g protein coupled receptor kinase 2 (grk2) inhibitor for the potential treatment of heart failure
75 266 7ayhA Crystal structure of aurora a in complex with 7-(2-anilinopyrimidin-4-yl)-1-benzazepin-2-one derivative (compound 2c)
98 322 6z3uB Structure of the cak complex form chaetomium thermophilum
81 281 7b31A Mst3 in complex with compound mria9
117 328 7a1zA Crystal structure of human protein kinase ck2alpha' (csnk2a2 gene product) in complex with the atp-competitive inhibitor 6-bromo-5-chloro-1h-triazolo[4,5-b]pyridine
102 322 6z4xB Structure of the cak complex form chaetomium thermophilum bound to atp-gamma-s
79 279 7b35A Mst3 in complex with compound mria13
90 293 7akgA Crystal structure of stk17b with bound dovitinib
111 350 6zqsA Crystal structure of double-phosphorylated p38alpha with atf2(83-102)
85 283 7b36A Mst4 in complex with compound g-5555
90 360 6zr5A Crystal structure of jnk1 in complex with atf2(19-58)
72 298 7kacA Crystal structure of hpk1 (map4k1) kinase in complex with 5-{[4-{[(1s)-2-hydroxy-1-phenylethyl]amino}-5-(1,3,4-oxadiazol-2-yl)pyrimidin-2-yl]amino}-3,3-dimethyl-2-benzofuran-1(3h)-one
99 347 7b6fA Gsk3-beta in complex with compound (s)-5c
115 334 7a49A Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 6-bromo-5-chloro-1h-triazolo[4,5-b]pyridine
78 268 7ayiA Crystal structure of aurora a in complex with 7-(2-anilinopyrimidin-4-yl)-1-benzazepin-2-one derivative (compound 2a)
85 281 7b32A Mst3 in complex with mria7
89 268 6xoeA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b(s1303d) in complex with atp
81 268 7kl1A Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b(s1303d) in complex with atp
113 327 7a1bA Crystal structure of human protein kinase ck2alpha' (csnk2a2 gene product) in complex with the atp-competitive inhibitor 5,6-dibromo-1h-triazolo[4,5-b]pyridine
109 338 6z08A Crystal structure of camp-dependent protein kinase a (cho pka) in complex with 4-nitrophenol
115 325 7a2hA Crystal structure of human protein kinase ck2alpha' (csnk2a2 gene product) in complex with the atp-competitive inhibitor 5,6,7-tribromo-1h-imidazo[4,5-b]pyridine
110 338 6zn0A Crystal structure of camp-dependent protein kinase a (cho pka) in complex with isonicotinamidine
112 333 7a4bA Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 5,6-dibromo-1h-triazolo[4,5-b]pyridine
122 333 6tluAAA Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5-dibromobenzotriazole
129 333 6tlsA Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,6-dibromobenzotriazole
83 273 6vruA Pim-inhibitor complex 1
94 401 6w3eA Structure of phosphorylated ire1 in complex with g-0701
127 402 6w3kA Structure of unphosphorylated human ire1 bound to g-9807
83 268 6x8vA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and tiam1
79 268 6xbxA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b in complex with atp
86 267 6x5qA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glua1
128 402 6w3bA Structure of apo unphosphorylated ire1
90 344 6v2wB Crystal structure of the braf:mek1 kinases in complex with amppnp
90 342 6v31B Crystal structure of the braf:mek1 kinases in complex with amppnp and ch5126766
82 271 6vrvA Discovery of sarxxxx92, a pan-pim kinase inhibitor, efficacious in a kg1 tumor model
96 403 6w3aA Structure of unphosphorylated ire1 in complex with g-7658
88 324 6z45A Cdk9-cyclin-t1 complex bound by compound 24
94 342 6v2zB Crystal structure of the braf:mek1 kinases in complex with amppnp and cobimetinib
125 405 6w3cA Structure of phosphorylated apo ire1
122 401 6w39A Structure of unphosphorylated ire1 in complex with g-1749
92 268 6x5gA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and lrrc7 inhibitory domain
98 346 6v2vB Crystal structure of the braf:mek1 kinases in complex with amppnp and pd0325901
86 343 6v2xB Crystal structure of the braf:mek1 kinases in complex with amppnp and binimetinib
128 333 6tlvA Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5-bromobenzotriazole
71 405 6wjfA Pka riibeta holoenzyme with dnajb1-pkac fusion in fibrolamellar hepatoceullar carcinoma
126 333 6tloA Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6-tribromobenzotriazole
88 344 6v30B Crystal structure of the braf:mek1 kinases in complex with amppnp and pimasertib
93 268 6xdlA Cocrystal structure of human camkii-alpha (camk2a)kinase domain and glun2b
88 340 6v2yB Crystal structure of the braf:mek1 kinases in complex with amppnp and trametinib
48 310 6wjgA Pka riibeta holoenzyme with dnajb1-pkac fusion in fibrolamellar hepatoceullar carcinoma