PDB Information

PDB5F4N
MethodX-RAY DIFFRACTION
Host Organism
Gene Source
Primary Citation
Multiparameter Lead Optimization to Give an Oral Checkpoint Kinase 1 (CHK1) Inhibitor Clinical Candidate: (R)-5-((4-((Morpholin-2-ylmethyl)amino)-5-(trifluoromethyl)pyridin-2-yl)amino)pyrazine-2-carbonitrile (CCT245737).
Osborne, J.D., Matthews, T.P., McHardy, T., Proisy, N., Cheung, K.M., Lainchbury, M., Brown, N., Walton, M.I., Eve, P.D., Boxall, K.J., Hayes, A., Henley, A.T., Valenti, M.R., De Haven Brandon, A.K., Box, G., Jamin, Y., Robinson, S.P., Westwood, I.M., van Montfort, R.L., Leonard, P.M., Lamers, M.B., Reader, J.C., Aherne, G.W., Raynaud, F.I., Eccles, S.A., Garrett, M.D., Collins, I.
J.Med.Chem.
HeaderTransferase
Released2015-12-03
Resolution1.910
CATH Insert Date05 Jun, 2016

PDB Images (4)

PDB Prints

PDB Chains (1)

Chain ID Date inserted into CATH CATH Status
A 06 Jun, 2016 Chopped

CATH Domains (2)

Domain ID Date inserted into CATH Superfamily CATH Status
5f4nA01 15 Jul, 2016 3.30.200.20 Assigned
5f4nA02 15 Jul, 2016 1.10.510.10 Assigned

UniProtKB Entries (1)

Accession Gene ID Taxon Description
O14757 CHK1_HUMAN Homo sapiens Serine/threonine-protein kinase Chk1