Found 4147 chains in Genus chains table. Displaying 51 - 100. Applied filters: Proteins

Search results query: Phosphorylase Kinase; domain 1

Total Genus Sequence Length pdb Title
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
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
88 276 5m51A Nek2 bound to arylaminopurine compound 8
70 256 5m09A Crystal structure of mycobacterium tuberculosis pkni kinase domain, c20a_r136n double mutant
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)
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
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)
94 290 5l3aA Fragment-based discovery of 6-arylindazole jak inhibitors
72 341 5kkrC Ksr2:mek1 complex bound to the small molecule aps-2-79
94 314 5kmmA Trka jm-kinase with 1-(2-methyl-4-phenyl-pyrimidin-5-yl)-3-(1-naphthyl)urea
85 279 5ko1A Pseudokinase domain of mlkl bound to compound 4.
95 323 5kmlA Trka jm-kinase with 1-(5-methyl-3-phenyl-1,2-oxazol-4-yl)-3-[[2-(trifluoromethyl)phenyl]methyl]urea
98 297 5kx8A Irak4-inhibitor co-structure
90 315 5kmkA Trka jm-kinase with 2-fluoro-{n}-[2-(4-fluorophenyl)-6-methyl-3-pyridyl]-4-(trifluoromethyl)benzamide
88 298 5l2wA The x-ray co-crystal structure of human cdk2/cycline and dinaciclib.
78 276 5knjA Pseudokinase domain of mlkl bound to compound 1.
68 292 5l2iA The x-ray co-crystal structure of human cdk6 and palbociclib.
93 323 5kmnA Trka jm-kinase with 1-(2-methyl-4-phenyl-pyrimidin-5-yl)-3-[[2-(trifluoromethyl)phenyl]methyl]urea
80 291 5l2sA The x-ray co-crystal structure of human cdk6 and abemaciclib.
86 298 5kmoA Trka jm-kinase with 1-(2-methyl-4-phenyl-pyrimidin-5-yl)-3-(2-pyridyl)urea
76 291 5l2tA The x-ray co-crystal structure of human cdk6 and ribociclib.
52 283 5kkrB Ksr2:mek1 complex bound to the small molecule aps-2-79
94 310 5kmjA Trka jm-kinase with {n}-(2-pyridylmethyl)-2-[2-(2-thienyl)indol-1-yl]acetamide
91 265 5kupA Bruton's tyrosine kinase (btk) with pyridazinone compound 9
95 311 5kmiA Trka jm-kinase with 1-(9{h}-fluoren-9-yl)-3-(2-methyl-4-phenyl-pyrimidin-5-yl)urea
73 306 5jk3A Crystal structure of tl11-128 bound to tak1-tab1
85 305 5jfxA Crystal structure of trka in complex with pf-06273340
81 301 5jebA Crystal structure of egfr tyrosine kinase domain with novel inhibitor of active state of her2
89 288 5khxA Crystal structure of jak1 in complex with pf-4950736
107 348 5k5xA Crystal structure of human pdgfra
139 464 5jmsA Crystal structure of tgcdpk1 bound to cgp060476
77 296 5jq8A Crystal structure of cdk2 in complex with inhibitor icec0943
97 307 5jgaA Crystal structure of human tak1/tab1 fusion protein in complex with ligand 11c
88 306 5jgdA Crystal structure of human tak1/tab1 fusion protein in complex with ligand 12
75 288 5kbrA Pak1 in complex with 7-azaindole inhibitor
83 299 5k4jA Crystal structure of cdk2 in complex with compound 22
82 277 5jsmA Brafv600e kinase domain in complex with chemically linked vemurafenib inhibitor vem-3-vem
75 298 5jkgA The crystal structure of fgfr4 kinase domain in complex with ly2874455
84 305 5jfvA Crystal structure of trka in complex with pf-05206283
88 323 5j9yA Egfr-t790m in complex with pyrazolopyrimidine inhibitor 1b
90 433 5kcvA Crystal structure of allosteric inhibitor, arq 092, in complex with autoinhibited form of akt1
116 350 5k4iA Crystal structure of erk2 in complex with compound 22
83 273 5jrqA Brafv600e kinase domain in complex with chemically linked vemurafenib inhibitor vem-6-vem
81 296 5jq5A Crystal structure of cdk2 in complex with inhibitor icec0942
86 305 5jfwA Crystal structure of trka in complex with pf-05247452
87 307 5jgbA Crystal structure of human tak1/tab1 fusion protein in complex with ligand 10