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4CKR

Crystal structure of the human DDR1 kinase domain in complex with DDR1-IN-1

Replaces:  4BKI
Summary for 4CKR
Entry DOI10.2210/pdb4ckr/pdb
DescriptorEPITHELIAL DISCOIDIN DOMAIN-CONTAINING RECEPTOR 1, 4-[(4-ethylpiperazin-1-yl)methyl]-n-{4-methyl-3-[(2-oxo-2,3-dihydro-1h-indol-5-yl)oxy]phenyl}-3-(trifluoromethyl)benzamide, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordstransferase, collagen, discoidin domain
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationIsoform 1: Cell membrane; Single-pass type I membrane protein. Isoform 2: Cell membrane; Single-pass type I membrane protein. Isoform 3: Secreted . Isoform 4: Cell membrane; Single-pass type I membrane protein: Q08345
Total number of polymer chains1
Total formula weight36617.02
Authors
Primary citationKim, H.,Tan, L.,Weisberg, E.L.,Liu, F.,Canning, P.,Choi, H.G.,Ezell, S.A.,Wu, H.,Zhao, Z.,Wang, J.,Mandinova, A.,Griffin, J.D.,Bullock, A.N.,Liu, Q.,Lee, S.W.,Gray, N.S.
Discovery of a Potent and Selective Ddr1 Receptor Tyrosine Kinase Inhibitor.
Acs Chem.Biol., 8:2145-, 2013
Cited by
PubMed: 23899692
DOI: 10.1021/CB400430T
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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