Search results query: Transferase(Phosphotransferase); domain 1

Found 4011 chains in Genus chains table. Displaying 2001 - 2050. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
83	278	4fttA	Crystal structure of the chk1
85	281	4fzaB	Crystal structure of mst4-mo25 complex
80	278	4fsmA	Crystal structure of the chk1
85	274	4fvqA	Crystal structure of the jak2 pseudokinase domain (mg-atp-bound form)
105	347	4fuxA	Crystal structure of the erk2 complexed with e75
79	268	4ftqA	Crystal structure of the chk1
83	274	4fvrA	Crystal structure of the jak2 pseudokinase domain mutant v617f (mg-atp-bound form)
82	278	4fsqA	Crystal structure of the chk1
86	274	4fvpA	Crystal structure of the jak2 pseudokinase domain (apo form)
98	349	4fv5A	Crystal structure of the erk2 complexed with ek9
79	278	4ft3A	Crystal structure of the chk1
93	302	4g17A	Crystal structure of ck1g3 with 2-[(4-tert-butylphenyl)amino]-1h-benzimidazole-6-carbonitrile
81	269	4ftoA	Crystal structure of the chk1
88	277	4fz6A	Crystal structure of spleen tyrosine kinase complexed with [6-((s)-2-methyl-pyrrolidin-1-yl)-pyridin-2-yl]-(6-phenyl-imidazo[1,2-b]pyridazin-8-yl)-amine
105	346	4fv1A	Crystal structure of the erk2 complexed with ek4
81	278	4fszA	Crystal structure of the chk1
98	310	4focA	Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 2
72	279	4ficA	Kinase domain of csrc in complex with a hinge region-binding fragment
83	298	3r6xA	Cdk2 in complex with inhibitor kvr-1-158
66	264	3r22A	Design, synthesis, and biological evaluation of pyrazolopyridine-sulfonamides as potent multiple-mitotic kinase (mmk) inhibitors (part i)
67	271	4fk3A	B-raf kinase v600e oncogenic mutant in complex with plx3203
79	298	3qziA	Cdk2 in complex with inhibitor kvr-1-126
94	292	4fijA	Catalytic domain of human pak4
93	302	4fnyA	Crystal structure of the r1275q anaplastic lymphoma kinase catalytic domain in complex with a benzoxazole inhibitor
81	275	4fc0A	Crystal structure of human kinase domain of b-raf with a dfg-out inhibitor
72	299	3r2bA	Mk2 kinase bound to compound 5b
83	298	4fkvA	Crystal structure of the cdk2 in complex with oxindole inhibitor
90	316	3r1nA	Mk3 kinase bound to compound 5b
78	298	4fkrA	Crystal structure of the cdk2 in complex with oxindole inhibitor
81	298	3r1sA	Cdk2 in complex with inhibitor kvr-1-127
67	279	4feqA	Inhibitor bound structure of the kinase domain of the murine receptor tyrosine kinase tyro3 (sky)
100	310	4fobA	Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 1
117	333	4fbxA	Complex structure of human protein kinase ck2 catalytic subunit crystallized in the presence of a bisubstrate inhibitor
83	298	3r71A	Cdk2 in complex with inhibitor kvr-1-162
79	298	4fkjA	Crystal structure of the cdk2 in complex with aminopyrazole inhibitor
80	298	3r28A	Cdk2 in complex with inhibitor kvr-1-140
77	296	4fksA	Crystal structure of the cdk2 in complex with oxindole inhibitor
93	294	4fifA	Catalytic domain of human pak4 with rpkplvdp peptide
82	298	3qzgA	Cdk2 in complex with inhibitor jws-6-76
111	350	4fmqA	Crystal structure of human erk2 complexed with a mapk docking peptide
85	290	4fgbA	Crystal structure of human calcium/calmodulin-dependent protein kinase i apo form
74	269	4fg7A	Crystal structure of human calcium/calmodulin-dependent protein kinase i 1-293 in complex with atp
80	298	4fkwA	Crystal structure of the cdk2 in complex with oxindole inhibitor
83	298	4fkpA	Crystal structure of the cdk2 in complex with oxindole inhibitor
84	298	3r1yA	Cdk2 in complex with inhibitor kvr-1-134
82	298	4fkgA	Crystal structure of the cdk2 in complex with aminopyrazole inhibitor
80	271	3r02A	The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors
85	377	4fieA	Full-length human pak4
102	322	4fnwA	Crystal structure of the apo f1174l anaplastic lymphoma kinase catalytic domain
57	195	3r7gA	Crystal structure of spire kind domain in complex with the tail of fmn2