PDB Information

PDB3L16
MethodX-RAY DIFFRACTION
Host OrganismSpodoptera frugiperda
Gene SourceHomo sapiens
Primary Citation
Discovery of (Thienopyrimidin-2-yl)aminopyrimidines as Potent, Selective, and Orally Available Pan-PI3-Kinase and Dual Pan-PI3-Kinase/mTOR Inhibitors for the Treatment of Cancer.
Sutherlin, D.P., Sampath, D., Berry, M., Castanedo, G., Chang, Z., Chuckowree, I., Dotson, J., Folkes, A., Friedman, L., Goldsmith, R., Heffron, T., Lee, L., Lesnick, J., Lewis, C., Mathieu, S., Nonomiya, J., Olivero, A., Pang, J., Prior, W.W., Salphati, L., Sideris, S., Tian, Q., Tsui, V., Wan, N.C., Wang, S., Wiesmann, C., Wong, S., Zhu, B.Y.
J.Med.Chem.
HeaderTransferase
Released2009-12-10
Resolution2.900
CATH Insert Date18 Feb, 2010

PDB Images (7)

PDB Prints

PDB Chains (1)

Chain ID Date inserted into CATH CATH Status
A 18 Feb, 2010 Chopped

CATH Domains (5)

Domain ID Date inserted into CATH Superfamily CATH Status
3l16A01 01 Jul, 2010 3.10.20.90 Assigned
3l16A02 01 Jul, 2010 2.60.40.150 Assigned
3l16A03 01 Jul, 2010 1.25.40.70 Assigned
3l16A04 01 Jul, 2010 3.30.1010.10 Assigned
3l16A05 01 Jul, 2010 1.10.1070.11 Assigned

UniProtKB Entries (1)

Accession Gene ID Taxon Description
P48736 PK3CG_HUMAN Homo sapiens Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
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