Found 3795 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: Pkinase

Total Genus Sequence Length pdb Title
102 356 7s1nA N-aromatic-substituted indazole derivatives as brain penetrant and orally bioavailable jnk3 inhibitors
84 320 7nwkA Crystal structure of cdk9-cyclin t1 bound by compound 6
107 339 7a5nA Structure of dyrk1a in complex with compound 34
117 341 7a52A Structure of dyrk1a in complex with compound 6
115 335 7a51A Structure of dyrk1a in complex with compound 5
119 346 7a5bA Structure of dyrk1a in complex with complex 10
91 333 7a4sA Structure of dyrk1a in complex with compound 2
83 273 7oowA Crystal structure of pim1 in complex with arc-1415
85 273 7oovA Crystal structure of pim1 in complex with arc-1411
110 346 7nqqA Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
101 345 7nr9A Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
113 346 7nr8A Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
114 346 7nqwA Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
109 347 7nr5A Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
109 346 7nr3A Discovery of astx029, a clinical candidate which modulates the phosphorylation and catalytic activity of erk1/2
117 442 7nh5A Co-crystal structure of akt1 in complex with covalent-allosteric akt inhibitor 6
54 290 7nj0B Cryoem structure of the human separase-cdk1-cyclin b1-cks1 complex
114 441 7nh4A Co-crystal structure of akt1 in complex with covalent-allosteric akt inhibitor 3
67 276 7naaA Crystal structure of mycobacterium tuberculosis h37rv pknf kinase domain
82 278 7n3uA Crystal structure of human wee1 kinase domain in complex with zn-c3
120 346 7a4oA Structure of dyrk1a in complex with ampnp
75 295 7lvhA Crystal structure of ap2 associated kinase 1 isoform 1 complexed with ligand n-[3-methoxy-4-(1,3-oxazol-5-yl)phenyl]-3-(propan-2-yl)piperidine-2-carboxamide
83 297 7lviA Crystal structure of ap2 associated kinase 1 isoform 1 complexed with ligand (2r)-2-amino-n-[3-methoxy-4- (1,3-oxazol-5-yl)phenyl]-4-methylpentanamide
101 328 7l1xA Structure of human ck2 alpha kinase (catalytic subunit) with the inhibitor 108600.
79 268 7kx6A Crystal structure of dclk1-kd in complex with xmd8-85
69 267 7kxwA Crystal structure of dclk1-kd in complex with dclk1-in-1
73 268 7kxwB Crystal structure of dclk1-kd in complex with dclk1-in-1
64 288 7kx8A Crystal structure of dclk1-cter in complex with fmf-03-055-1
120 340 7a4rA Structure of dyrk1a in complex with compound 1
79 484 7jijA Atp-bound amp-activated protein kinase
72 273 7f3gA Crystal structure of dclk1 kinase domain in complex with ruxolitinib
91 292 7cp4A Crystal structure of pak4 in complex with inhibitor 55
72 290 7cp3A Crystal structure of pak4 in complex with inhibitor 47
140 406 7bmkA Atp-competitive partial antagonists-'pair's-rheostatically modulate ire1alpha's kinase helix-alphac to segregate its rnase-mediated biological outputs
80 293 7b7sA Cdk2/cyclin a2 in complex with 3h-pyrazolo[4,3-f]quinoline-based derivative hsd1368
113 328 7atvA Structure of protein kinase ck2 catalytic subunit (csnk2a2 gene product) in complex with the bivalent inhibitor kn2
111 347 7auvA The structure of erk2 in complex with dual inhibitor astx029
108 430 7apjA Structure of autoinhibited akt1 reveals mechanism of pip3-mediated activation
111 328 7at9A Structure of protein kinase ck2 catalytic subunit (csnk2a2 gene product) in complex with the atp-competitive inhibitor mb002 and the alphad-pocket ligand 3,4-dichlorophenethylamine
117 332 7at5A Structure of protein kinase ck2 catalytic subunit (csnk2a1 gene product) in complex with the bivalent inhibitor kn2
117 347 6ln1A A natural inhibitor of dyrk1a for treatment of diabetes mellitus
82 320 6w9eA Crystal structure of human cdk9/cyclint1 in complex with mc180295
80 306 7ooxA Crystal structure of pim1 in complex with arc-3126
92 316 7p1lA The mark3 kinase domain bound to aa-cs-1-008
111 357 7orfA Crystal structure of jnk3 in complex with fmu-001-367 (compound 1)
111 359 7oreA Crystal structure of jnk3 in complex with light-activated covalent inhibitor mr-ii-249 with both non-covalent and covalent binding modes (compound 4)
113 337 7opgA Crystal structure of clk1 in complex with compound 2 (cc513)
64 484 7jhhA Cryo-em structure of atp-bound fully inactive ampk in complex with fab and nanobody
73 484 7jhgA Cryo-em structure of atp-bound fully inactive ampk in complex with dorsomorphin (compound c) and fab-nanobody
88 291 7cmbA Crystal structure of pak4 in complex with inhibitor 41