PDB Information

PDB4EWH
MethodX-RAY DIFFRACTION
Host Organism
Gene SourceHomo sapiens
Primary Citation
Synthesis and optimization of substituted furo[2,3-d]-pyrimidin-4-amines and 7H-pyrrolo[2,3-d]pyrimidin-4-amines as ACK1 inhibitors.
Jiao, X., Kopecky, D.J., Liu, J., Liu, J., Jaen, J.C., Cardozo, M.G., Sharma, R., Walker, N., Wesche, H., Li, S., Farrelly, E., Xiao, S.H., Wang, Z., Kayser, F.
Bioorg.Med.Chem.Lett.
HeaderTransferase/Transferase Inhibitor
Released2012-04-27
Resolution2.500
CATH Insert Date04 Nov, 2012

PDB Images (7)

PDB Prints

PDB Chains (2)

Chain ID Date inserted into CATH CATH Status
A 05 Nov, 2012 Chopped
B 05 Nov, 2012 Chopped

CATH Domains (4)

Domain ID Date inserted into CATH Superfamily CATH Status
4ewhA01 14 Aug, 2013 3.30.200.20 Assigned
4ewhA02 14 Aug, 2013 1.10.510.10 Assigned
4ewhB01 14 Aug, 2013 3.30.200.20 Assigned
4ewhB02 14 Aug, 2013 1.10.510.10 Assigned

UniProtKB Entries (2)

Accession Gene ID Taxon Description
Q07912 ACK1_HUMAN Homo sapiens Activated CDC42 kinase 1
Q07912 ACK1_HUMAN Homo sapiens Activated CDC42 kinase 1