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7AVY

MerTK kinase domain in complex with quinazoline-based inhbitor

Summary for 7AVY
Entry DOI10.2210/pdb7avy/pdb
DescriptorTyrosine-protein kinase Mer, N-(2-(2-cyclopropylethoxy)pyrimidin-5-yl)-7-methoxy-6-(piperidin-4-ylmethoxy)quinazolin-4-amine, SULFATE ION, ... (4 entities in total)
Functional Keywordstyrosine kinase, inhibitor, type1.5 kinase inhibitor, structure-based drug design, oncology, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight34739.08
Authors
Primary citationNissink, J.W.M.,Bazzaz, S.,Blackett, C.,Clark, M.A.,Collingwood, O.,Disch, J.S.,Gikunju, D.,Goldberg, K.,Guilinger, J.P.,Hardaker, E.,Hennessy, E.J.,Jetson, R.,Keefe, A.D.,McCoull, W.,McMurray, L.,Olszewski, A.,Overman, R.,Pflug, A.,Preston, M.,Rawlins, P.B.,Rivers, E.,Schimpl, M.,Smith, P.,Truman, C.,Underwood, E.,Warwicker, J.,Winter-Holt, J.,Woodcock, S.,Zhang, Y.
Generating Selective Leads for Mer Kinase Inhibitors-Example of a Comprehensive Lead-Generation Strategy.
J.Med.Chem., 64:3165-3184, 2021
Cited by
PubMed: 33683117
DOI: 10.1021/acs.jmedchem.0c01904
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.31 Å)
Structure validation

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