Found 4011 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: Transferase(Phosphotransferase); domain 1

Total Genus Sequence Length pdb Title
216 695 4oauC Complete human rnase l in complex with biological activators.
224 694 4oavB Complete human rnase l in complex with 2-5a (5'-ppp heptamer), amppcp and rna substrate.
166 627 3uztA Structure of the c13.18 rna aptamer in complex with g protein-coupled receptor kinase 2
102 356 4ux9A Crystal structure of jnk1 bound to a mkk7 docking motif
83 306 5j9lA Crystal structure of cpt1691 bound to tak1-tab1
114 338 5j1wA Crystal structure of human clk1 in complex with pyrido[3,4-g]quinazoline derivative zw31 (compound 14)
113 338 5j1vA Crystal structure of human clk1 in complex with pyrido[3,4-g]quinazoline derivative zw29 (compound 13)
81 276 3tucA Crystal structure of syk kinase domain with 1-benzyl-n-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-1,2-dihydropyridine-3-carboxamide
76 263 3uojA Aurora a in complex with rpm1715
87 301 3u6hA Crystal structure of c-met in complex with pyrazolone inhibitor 26
158 464 3upzA Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with bumpless bki analog uw1243
103 310 3u6jA Crystal structure of the vegfr2 kinase domain in complex with a pyrazolone inhibitor
84 272 3tubA Crystal structure of syk kinase domain with 1-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-3-((1r,2s)-2-phenylcyclopropyl)urea
82 267 3uo5A Aurora a in complex with yl1-038-31
84 274 3tudA Crystal structure of syk kinase domain with n-(4-methyl-3-(8-methyl-7-oxo-2-(phenylamino)-7,8-dihydropyrido[2,3-d]pyrimidin-6-yl)phenyl)-3-(trifluoromethyl)benzamide
65 246 3uqcA Structure of the intracellular kinase homology domain of rv3910 at 2.2 a resolution
86 301 3u6iA Crystal structure of c-met in complex with pyrazolone inhibitor 58a
79 276 3uqfA C-src kinase domain in complex with bki rm-1-89
82 298 3unkA Cdk2 in complex with inhibitor yl5-083
85 277 3svvA Crystal structure of t338c c-src covalently bound to vinylsulfonamide-pyrazolopyrimidine 9
75 298 3s0oA Cdk2 in complex with inhibitor rc-1-138
80 298 3s00A Cdk2 in complex with inhibitor l4-14
78 298 3s1hA Cdk2 in complex with inhibitor rc-2-39
107 357 3sa0A Complex of erk2 with norathyriol
85 298 3sw7A Crystal structure of the cdk2 in complex with thiazolylpyrimidine inhibitor
113 332 5m4uA Orthorhombic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro- flavonol (flc21)
116 331 5m56A Monoclinic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro-flavonol (flc21)
115 329 5m4cA Complex structure of human protein kinase ck2 catalytic subunit with a thieno[2,3-d]pyrimidin inhibitor crystallized under low-salt conditions
80 277 5m57A Nek2 bound to arylaminopurine 6
90 272 5m53A Nek2 bound to arylaminopurine inhibitor 11
95 290 5lwnA Crystal structure of jak3 in complex with compound 5 (fm409)
84 267 5lxmA Crystal structure of aurora-a bound to a hydrocarbon-stapled proteomimetic of tpx2
83 284 5lvmA Human pdk1 kinase domain in complex with adenine bound to the atp-binding site
101 329 5m44A Complex structure of human protein kinase ck2 catalytic subunit with a thieno[2,3-d]pyrimidin inhibitor crystallized under high-salt conditions
85 285 5lvpA Human pdk1 kinase domain in complex with an hm-peptide bound to the pif-pocket
89 271 5lmbA Human spleen tyrosine kinase kinase domain in complex with azanaphthyridine inhibitor
85 264 5l8lA Aurora-a kinase domain in complex with vnar-d01 (crystal form 1)
82 292 5lqfA Cdk1/cyclinb1/cks2 in complex with nu6102
96 290 5lwmA Crystal structure of jak3 in complex with compound 4 (fm381)
86 274 5l6oA Ephb3 kinase domain covalently bound to an irreversible inhibitor (compound 3)
57 284 5lohA Kinase domain of human greatwall
112 347 5lcjA In-gel activity-based protein profiling of a clickable covalent erk 1/2 inhibitor
112 331 5m4iA Complex structure of human protein kinase ck2 catalytic subunit with the inhibitor 4'-carboxy-6,8-chloro-flavonol (flc21) crystallized under high-salt conditions
86 299 5lmkA Structure of phopsho-cdk2-cyclin a in complex with an atp-competitive inhibitor
89 267 5l8kA Aurora-a kinase domain in complex with vnar-d01 (crystal form 2)
117 330 5m4fA Complex structure of human protein kinase ck2 catalytic subunit with the inhibitor 4'-carboxy-6,8-chloro-flavonol (flc21) crystallized under low-salt conditions
84 286 5lvoA Human pdk1 kinase domain in complex with allosteric compound pse10 bound to the pif-pocket
67 281 5ljjA Crystal structure of human mps1 (ttk) in complex with reversine
83 274 5l6pA Ephb3 kinase domain covalently bound to an irreversible inhibitor (compound 6)
88 276 5m51A Nek2 bound to arylaminopurine compound 8