Found 4147 chains in Genus chains table. Displaying 2801 - 2850. Applied filters: Proteins

Search results query: Phosphorylase Kinase; domain 1

Total Genus Sequence Length pdb Title
89 270 3dk7A Crystal structure of mutant abl kinase domain in complex with small molecule fragment
78 275 3dqxA Chicken c-src kinase domain in complex with atpgs
83 299 3dogA Structure of thr 160 phosphorylated cdk2/cyclin a in complex with the inhibitor n-&-n1
93 312 3dkfA Structure of met receptor tyrosine kinase in complex with inhibitor sgx-523
105 338 3dneA Camp-dependent protein kinase pka catalytic subunit with pki-5-24
85 296 3dkoA Complex between the kinase domain of human ephrin type-a receptor 7 (epha7) and inhibitor alw-ii-49-7
77 274 3dcvA Crystal structure of human pim1 kinase complexed with 4-(4-hydroxy-3-methyl-phenyl)-6-phenylpyrimidin-2(1h)-one
86 312 3dpkA Cfms tyrosine kinase in complex with a pyridopyrimidinone inhibitor
74 285 3dlsA Crystal structure of human pas kinase bound to adp
101 312 3dkcA Structure of met receptor tyrosine kinase in complex with atp
93 293 3dfcB Crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain with amppnp
85 299 3ddqA Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor roscovitine
105 336 3dndA Camp-dependent protein kinase pka catalytic subunit with pki-5-24
91 307 3dkgA Structure of mutant(y1248l) met receptor tyrosine kinase in complex with inhibitor sgx-523
79 263 3dj7A Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 130.
85 298 3ddpA Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor cr8
84 270 3dk6A Crystal structure of mutant abl kinase domain in complex with small molecule fragment
81 270 3dfaA Crystal structure of kinase domain of calcium-dependent protein kinase cgd3_920 from cryptosporidium parvum
76 261 3dj5A Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 290.
76 261 3dj6A Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 823.
112 329 3dlzA Crystal structure of human haspin in complex with amp
87 270 3dk3A Crystal structure of mutant abl kinase domain in complex with small molecule fragment
85 292 3dgkA Crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain
111 349 3d7zA Crystal structure of p38 kinase in complex with a biphenyl amide inhibitor
68 288 3d5vA Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain.
86 269 3d14A Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)-ethyl]- thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea
74 287 3dbfA Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 562
77 287 3d5wA Crystal structure of a phosphorylated polo-like kinase 1 (plk1) catalytic domain in complex with adp.
76 288 3d5uA Crystal structure of a wildtype polo-like kinase 1 (plk1) catalytic domain.
72 287 3dbcA Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 257
73 287 3dbdA Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 094
108 400 3d9vA Crystal structure of rock i bound to h-1152p a di-methylated variant of fasudil
72 276 3d7tB Structural basis for the recognition of c-src by its inactivator csk
80 276 3d4qA Pyrazole-based inhibitors of b-raf kinase
103 335 3d0eA Crystal structure of human akt2 in complex with gsk690693
108 349 3d83A Crystal structure of p38 kinase in complex with a biphenyl amide inhibitor
95 300 3d94A Crystal structure of the insulin-like growth factor-1 receptor kinase in complex with pqip
70 287 3db8A Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 041
67 268 3daeA Crystal structure of phosphorylated snf1 kinase domain
82 274 3cxwA Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand i
104 356 3da6A Crystal structure of human jnk3 complexed with n-(3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)naphthalen-1-yl)-1h-benzo[d]imidazol-2-amine
85 290 3dakA Crystal structure of domain-swapped osr1 kinase domain
75 262 3d2iA Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(1-methyl-1h-pyrazolo[4,3-d]pyrimidin-7-ylamino)-ethyl]-thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea
82 273 3cy3A Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and the jnk inhibitor v
73 262 3dajA Crystal structure of aurora a complexed with an inhibitor discovered through site-directed dynamic tethering
71 286 3d5xA Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with wortmannin.
78 263 3d15A Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-(3-chloro-phenyl)-3-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)- ethyl]-thiazol-2-yl}-urea [sns-314]
80 273 3cy2A Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand ii
79 287 3db6A Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 902
61 263 3d7tA Structural basis for the recognition of c-src by its inactivator csk