Search results query: Transferase(Phosphotransferase); domain 1

Found 4011 chains in Genus chains table. Displaying 2051 - 2100. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
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
109	327	3r0tA	Crystal structure of human protein kinase ck2 alpha subunit in complex with the inhibitor cx-5279
83	298	4fkiA	Crystal structure of the cdk2 in complex with aminopyrazole inhibitor
93	292	4fihA	Catalytic domain of human pak4 with qkftglprqw peptide
80	298	3qzhA	Cdk2 in complex with inhibitor kvr-1-124
100	321	4fodA	Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 36
53	218	4ff8A	Inhibitor bound structure of the kinase domain of the murine receptor tyrosine kinase tyro3 (sky)
76	296	4fktA	Crystal structure of the cdk2 in complex with oxindole inhibitor
73	300	3r2yA	Mk2 kinase bound to compound 1
86	273	4fl1A	Structural and biophysical characterization of the syk activation switch
79	274	3r01A	The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors
96	292	4fiiA	Catalytic domain of human pak4 with rpkplvdp peptide
78	305	4fg9A	Crystal structure of human calcium/calmodulin-dependent protein kinase i 1-320 in complex with atp
82	298	4fkuA	Crystal structure of the cdk2 in complex with oxindole inhibitor
85	292	4fk6A	Jak1 kinase (jh1 domain) in complex with compound 72
81	271	3r04A	The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors
91	293	4figA	Catalytic domain of human pak4
180	627	4fl3A	Structural and biophysical characterization of the syk activation switch
114	346	3qywA	Crystal structure of erk2 in complex with an inhibitor
129	371	4fi1A	Crystal structure of scck2 alpha in complex with atp
79	274	3r00A	The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors
95	312	4fnxA	Crystal structure of the apo r1275q anaplastic lymphoma kinase catalytic domain
114	355	3r63A	Structure of erk2 (spe) mutant (s246e)
73	300	3r30A	Mk2 kinase bound to compound 2
87	298	4fklA	Crystal structure of the cdk2 in complex with thiazolylpyrimidine inhibitor
80	298	3r1qA	Cdk2 in complex with inhibitor kvr-1-102
179	627	4fl2A	Structural and biophysical characterization of the syk activation switch
75	290	4fg8A	Crystal structure of human calcium/calmodulin-dependent protein kinase i 1-315 in complex with atp
84	298	3r73A	Cdk2 in complex with inhibitor kvr-1-164
83	298	4fkoA	Crystal structure of the cdk2 in complex with thiazolylpyrimidine inhibitor
84	298	4fkqA	Crystal structure of the cdk2 in complex with oxindole inhibitor
88	263	3qrjA	The crystal structure of human abl1 kinase domain t315i mutant in complex with dcc-2036
82	274	3qf9A	Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a furan-thiazolidinedione ligand
106	349	3queA	Human p38 map kinase in complex with skepinone-l
81	286	3qcxA	Phosphoinositide-dependent kinase-1 (pdk1) kinase domain with 6-{2-amino-6-[(3r)-3-methyl-4-morpholinyl]-4-pyrimidinyl}-1h-indazol-3-amine
78	295	3qquA	Cocrystal structure of unphosphorylated igf with pyrimidine 8
103	414	3qfvA	Mrck beta in complex with tpca-1
83	298	3qtuA	Cdk2 in complex with inhibitor rc-2-132
78	298	3qu0A	Cdk2 in complex with inhibitor rc-2-38
78	332	3qd2B	Crystal structure of mouse perk kinase domain
84	270	3qrkA	The crystal structure of human abl1 kinase domain in complex with dp-987
78	298	3qqkA	Cdk2 in complex with inhibitor l4
81	298	3ql8A	Cdk2 in complex with inhibitor jws-6-260
73	298	3qzfA	Cdk2 in complex with inhibitor jws-6-52
86	298	3qhwA	Structure of a pcdk2/cyclina transition-state mimic
78	298	3qtzA	Cdk2 in complex with inhibitor rc-2-36
83	298	3qqfA	Cdk2 in complex with inhibitor l1
83	298	3qqjA	Cdk2 in complex with inhibitor l2
82	298	3qxoA	Cdk2 in complex with inhibitor kvr-1-84