Search results query: Transferase(Phosphotransferase); domain 1

Found 4011 chains in Genus chains table. Displaying 3651 - 3700. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
93	348	1y6aA	Crystal structure of vegfr2 in complex with a 2-anilino-5-aryl-oxazole inhibitor
77	273	1yojA	Crystal structure of src kinase domain
92	293	1yhvA	Crystal structure of pak1 kinase domain with two point mutations (k299r, t423e)
82	273	1yhsA	Crystal structure of pim-1 bound to staurosporine
79	298	1y8yA	Crystal structure of human cdk2 complexed with a pyrazolo[1,5-a]pyrimidine inhibitor
65	279	1yomA	Crystal structure of src kinase domain in complex with purvalanol a
92	350	1y6bA	Crystal structure of vegfr2 in complex with a 2-anilino-5-aryl-oxazole inhibitor
79	278	1yolA	Crystal structure of src kinase domain in complex with cgp77675
77	273	1yi3A	Crystal structure of pim-1 bound to ly294002
108	336	1ydrE	Structure of camp-dependent protein kinase, alpha-catalytic subunit in complex with h7 protein kinase inhibitor 1-(5-isoquinolinesulfonyl)-2-methylpiperazine
132	452	1y57A	Structure of unphosphorylated c-src in complex with an inhibitor
106	356	1yqjA	Crystal structure of p38 alpha in complex with a selective pyridazine inhibitor
76	273	1yi4A	Structure of pim-1 bound to adenosine
85	276	1yi6A	C-term tail segment of human tyrosine kinase (258-533)
109	336	1ydsE	Structure of camp-dependent protein kinase, alpha-catalytic subunit in complex with h8 protein kinase inhibitor [n-(2-methylamino)ethyl]-5-isoquinolinesulfonamide
91	293	1yhwA	Crystal structure of pak1 kinase domain with one point mutations (k299r)
82	277	1xqzA	Crystal structure of hpim-1 kinase at 2.1 a resolution
111	337	1xh5A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
87	320	1xjdA	Crystal structure of pkc-theta complexed with staurosporine at 2a resolution
108	338	1xh9A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
83	273	1xwsA	Crystal structure of the human pim1 kinase domain
87	317	1xkkA	Egfr kinase domain complexed with a quinazoline inhibitor- gw572016
107	340	1xh7A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
105	337	1xh4A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
112	339	1xh8A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
83	277	1xr1A	Crystal structure of hpim-1 kinase in complex with amp-pnp at 2.1 a resolution
108	333	1xh6A	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
69	295	1xo2B	Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin
115	350	1xhaA	Crystal structures of protein kinase b selective inhibitors in complex with protein kinase a and mutants
83	279	1x8bA	Structure of human wee1a kinase: kinase domain complexed with inhibitor pd0407824
78	273	1wvyA	Crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors
82	275	1wvwA	Crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors
87	275	1wvxA	Crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors
70	303	1wmkA	Human death-associated kinase drp-1, mutant s308d d40
86	274	1xbcA	Crystal structure of the syk tyrosine kinase domain with staurosporin
101	350	1wzyA	Crystal structure of human erk2 complexed with a pyrazolopyridazine derivative
107	347	1wfcA	Structure of apo, unphosphorylated, p38 mitogen activated protein kinase p38 (p38 map kinase) the mammalian homologue of the yeast hog1 protein
85	274	1xbaA	Crystal structure of apo syk tyrosine kinase domain
91	277	1xbbA	Crystal structure of the syk tyrosine kinase domain with gleevec
113	351	1wbtA	Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.
76	298	1wccA	Screening for fragment binding by x-ray crystallography
110	351	1w82A	P38 kinase crystal structure in complex with small molecule inhibitor
93	276	1w2fA	Human inositol (1,4,5)-trisphosphate 3-kinase substituted with selenomethionine
85	302	1vywA	Structure of cdk2/cyclin a with pnu-292137
102	372	1wbpA	Srpk1 bound to 9mer docking motif peptide
113	376	1wakA	X-ray structure of srpk1
82	298	1w8cA	Co-crystal structure of 6-cyclohexylmethoxy-8-isopropyl-9h-purin-2- ylamine and monomeric cdk2
79	298	1w0xC	Crystal structure of human cdk2 in complex with the inhibitor olomoucine.
111	351	1wbnA	Fragment based p38 inhibitors
112	351	1wbvA	Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.