PDB Information

PDB4IWD
MethodX-RAY DIFFRACTION
Host Organism
Gene SourceHomo sapiens
Primary Citation
Discovery of 1-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]-N-(pyridin-2-ylmethyl)methanesulfonamide (MK-8033): A Specific c-Met/Ron dual kinase inhibitor with preferential affinity for the activated state of c-Met.
Northrup, A.B., Katcher, M.H., Altman, M.D., Chenard, M., Daniels, M.H., Deshmukh, S.V., Falcone, D., Guerin, D.J., Hatch, H., Li, C., Lu, W., Lutterbach, B., Allison, T.J., Patel, S.B., Reilly, J.F., Reutershan, M., Rickert, K.W., Rosenstein, C., Soisson, S.M., Szewczak, A.A., Walker, D., Wilson, K., Young, J.R., Pan, B.S., Dinsmore, C.J.
J.Med.Chem.
HeaderTransferase/Transferase Inhibitor
Released2013-01-23
Resolution1.990
CATH Insert Date15 Dec, 2013

PDB Images (4)

PDB Prints

PDB Chains (1)

Chain ID Date inserted into CATH CATH Status
A 16 Dec, 2013 Chopped

CATH Domains (2)

Domain ID Date inserted into CATH Superfamily CATH Status
4iwdA01 20 Dec, 2013 3.30.200.20 Assigned
4iwdA02 20 Dec, 2013 1.10.510.10 Assigned

UniProtKB Entries (1)

Accession Gene ID Taxon Description
P08581 MET_HUMAN Homo sapiens Hepatocyte growth factor receptor