Search results query: Transferase(Phosphotransferase); domain 1

Found 4011 chains in Genus chains table. Displaying 3501 - 3550. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
83	264	2dwbA	Aurora-a kinase complexed with amppnp
69	268	2e9vA	Structure of h-chk1 complexed with a859017
89	278	2e2bA	Crystal structure of the c-abl kinase domain in complex with inno-406
97	324	2eb2A	Crystal structure of mutated egfr kinase domain (g719s)
94	323	2eb3A	Crystal structure of mutated egfr kinase domain (l858r) in complex with amppnp
79	269	2e9oA	Structure of h-chk1 complexed with aa582939
74	298	2ds1A	Human cyclin dependent kinase 2 complexed with the cdk4 inhibitor
68	263	2dq7X	Crystal structure of fyn kinase domain complexed with staurosporine
68	298	2duvA	Structure of cdk2 with a 3-hydroxychromones
85	300	2dylA	Crystal structure of human mitogen-activated protein kinase kinase 7 activated mutant (s287d, t291d)
102	336	2cpkE	Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase
86	271	2clqA	Structure of mitogen-activated protein kinase kinase kinase 5
86	297	2cchA	The crystal structure of cdk2 cyclin a in complex with a substrate peptide derived from cdc modified with a gamma-linked atp analogue
86	292	2cdzA	Crystal structure of the human p21-activated kinase 4 in complex with cgp74514a
88	293	2csnA	Binary complex of casein kinase-1 with cki7
94	296	2cmwA	Structure of human casein kinase 1 gamma-1 in complex with 2-(2- hydroxyethylamino)-6-(3-chloroanilino)-9-isopropylpurine
79	292	2cn8A	Crystal structure of human chk2 in complex with debromohymenialdisine
80	292	2cjmA	Mechanism of cdk inhibition by active site phosphorylation: cdk2 y15p t160p in complex with cyclin a structure
78	266	2cguA	Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening
77	267	2cgvA	Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening
81	298	2c69A	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
76	263	2c6eA	Aurora a kinase activated mutant (t287d) in complex with a 5- aminopyrimidinyl quinazoline inhibitor
84	269	2c3iB	Crystal structure of human pim1 in complex with imidazopyridazin i
84	297	2cn5A	Crystal structure of human chk2 in complex with adp
100	298	2chlA	Structure of casein kinase 1 gamma 3
77	298	2c6kA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
80	296	2c5vA	Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design
79	296	2c68A	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
82	298	2clxA	4-arylazo-3,5-diamino-1h-pyrazole cdk inhibitors: sar study, crystal structure in complex with cdk2, selectivity, and cellular effects
91	301	2ckeA	Human death-associated drp-1 kinase in complex with inhibitor
78	266	2cgwA	Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening
76	296	2c6oA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
86	296	2c6tA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
85	296	2c5oA	Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design
89	301	2c4gA	Structure of cdk2-cyclin a with pha-533514
75	268	2cgxA	Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening
77	297	2cciA	Crystal structure of phospho-cdk2 cyclin a in complex with a peptide containing both the substrate and recruitment sites of cdc6
81	298	2c6iA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
80	297	2c5yA	Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design
78	296	2c5xA	Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design
78	272	2c3lA	Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification
77	296	2c6mA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
80	296	2c5nA	Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design
78	264	2c6dA	Aurora a kinase activated mutant (t287d) in complex with adpnp
125	447	2c0tA	Src family kinase hck with bound inhibitor a-641359
78	265	2c3jA	Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification
77	298	2c6lA	Crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor
127	447	2c0iA	Src family kinase hck with bound inhibitor a-420983
84	273	2bziB	Crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru2
95	295	2c47A	Structure of casein kinase 1 gamma 2