Search results query: Phosphorylase Kinase; domain 1

Found 4147 chains in Genus chains table. Displaying 551 - 600. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
102	312	4asdA	Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sorafenib (bay 43-9006)
87	321	4bcgA	Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor
78	279	4bi2A	Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor
80	273	4as0A	Cyclometalated phthalimides as protein kinase inhibitors
99	303	4b9dA	Crystal structure of human nima-related kinase 1 (nek1) with inhibitor.
82	271	4bieA	Crystal structures of ask1-inhibitor complexes
92	281	4b6lA	Discovery of oral polo-like kinase (plk) inhibitors with enhanced selectivity profile using residue targeted drug design
80	299	4bckA	Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor
82	303	4bdcA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
76	282	4aw5A	Complex of the ephb4 kinase domain with an oxindole inhibitor
88	304	4bddA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
81	270	4bidA	Crystal structures of ask1-inhibitor complexes
83	299	4bcnA	Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor
78	294	4bgqA	Crystal structure of the human cdkl5 kinase domain
83	270	4bibA	Crystal structures of ask1-inhibitor complexes
80	322	4arkA	Crystal structure of the catalytic domain of human map kinase kinase 1 (mek1) in complex with a small molecule inhibitor and adp
77	279	4bhzA	Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor
126	432	4axcA	Inositol 1,3,4,5,6-pentakisphosphate 2-kinase apo form
87	304	4bdfA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
99	299	4at5A	Crystal structure of trkb kinase domain in complex with gw2580
78	293	4bc6A	Crystal structure of human serine threonine kinase-10 bound to novel bosutinib isoform 1, previously thought to be bosutinib
87	299	4bcpA	Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor
135	434	4axeA	Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with adp
91	296	4bggA	Crystal structure of the acvr1 kinase in complex with ldn-213844
152	470	4azsA	High resolution (2.2 a) crystal structure of wbdd.
87	303	4bdhA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
89	304	4bdeA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
79	285	4aw0A	Human pdk1 kinase domain in complex with allosteric compound ps182 bound to the pif-pocket
83	321	4bcjA	Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor
78	291	4auaA	Liganded x-ray crystal structure of cyclin dependent kinase 6 (cdk6)
84	271	4bicA	Crystal structures of ask1-inhibitor complexes
127	437	4aqkA	Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with adp and ip6
81	271	4bhnA	Crystal structures of ask1-inhibitor complexes
118	350	4azeA	Human dyrk1a in complex with leucettine l41
147	470	4ax8A	Medium resolution structure of the bifunctional kinase- methyltransferase wbdd
76	266	4b0gA	Complex of aurora-a bound to an imidazopyridine-based inhibitor
80	269	4bf2A	Crystal structures of ask1-inhibitor complexes
112	337	4axaA	Structure of pka-pkb chimera complexed with (1s)-2-amino-1-(4- chlorophenyl)-1-(4-(1h-pyrazol-4-yl)phenyl)ethan-1-ol
85	321	4bcfA	Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor
81	298	4bghA	Crystal structure of cdk2 in complex with pan-cdk inhibitor
95	299	4aszA	Crystal structure of apo trkb kinase domain
146	468	4aztA	Co-crystal structure of wbdd and kinase inhibitor ly294002.
82	322	4bciA	Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor
139	416	4aw2A	Crystal structure of cdc42 binding protein kinase alpha (mrck alpha)
85	303	4bdjA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
110	357	4awiA	Human jnk1alpha kinase with 4-phenyl-7-azaindole ikk2 inhibitor.
86	304	4bdaA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
148	470	4azvA	Co-crystal structure of wbdd and kinase inhibitor gw435821x.
85	307	4bdiA	Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2)
141	434	4axdA	Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with amppnp