PDB Information

PDB4EJN
MethodX-RAY DIFFRACTION
Host OrganismSpodoptera frugiperda
Gene SourceHomo sapiens
Primary Citation
Discovery and optimization of a series of 3-(3-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amines: orally bioavailable, selective, and potent ATP-independent Akt inhibitors.
Ashwell, M.A., Lapierre, J.M., Brassard, C., Bresciano, K., Bull, C., Cornell-Kennon, S., Eathiraj, S., France, D.S., Hall, T., Hill, J., Kelleher, E., Khanapurkar, S., Kizer, D., Koerner, S., Link, J., Liu, Y., Makhija, S., Moussa, M., Namdev, N., Nguyen, K., Nicewonger, R., Palma, R., Szwaya, J., Tandon, M., Uppalapati, U., Vensel, D., Volak, L.P., Volckova, E., Westlund, N., Wu, H., Yang, R.Y., Chan, T.C.
J.Med.Chem.
HeaderTransferase/Transferase Inhibitor
Released2012-04-06
Resolution2.190
CATH Insert Date27 May, 2012

PDB Images (5)

PDB Prints

PDB Chains (1)

Chain ID Date inserted into CATH CATH Status
A 28 May, 2012 Chopped

CATH Domains (3)

Domain ID Date inserted into CATH Superfamily CATH Status
4ejnA01 15 Nov, 2013 2.30.29.30 Assigned
4ejnA02 15 Nov, 2013 3.30.200.20 Assigned
4ejnA03 15 Nov, 2013 1.10.510.10 Assigned

UniProtKB Entries (1)

Accession Gene ID Taxon Description
P31749 AKT1_HUMAN Homo sapiens RAC-alpha serine/threonine-protein kinase
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