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5EYM

MEK1 IN COMPLEX WITH BI 847325

Summary for 5EYM
Entry DOI10.2210/pdb5eym/pdb
DescriptorDual specificity mitogen-activated protein kinase kinase 1, 3-[(3~{Z})-3-[[[4-[(dimethylamino)methyl]phenyl]amino]-phenyl-methylidene]-2-oxidanylidene-1~{H}-indol-6-yl]-~{N}-ethyl-prop-2-ynamide, CALCIUM ION, ... (4 entities in total)
Functional Keywordskinase, inhibitor, transferase
Biological sourceHomo sapiens (Human)
Cellular locationCytoplasm, cytoskeleton, microtubule organizing center, centrosome : Q02750
Total number of polymer chains2
Total formula weight81161.69
Authors
Bader, G.,Reiser, U.,Zahn, S.K.,Treu, M. (deposition date: 2015-11-25, release date: 2016-08-17, Last modification date: 2024-01-10)
Primary citationSini, P.,Gurtler, U.,Zahn, S.K.,Baumann, C.,Rudolph, D.,Baumgartinger, R.,Strauss, E.,Haslinger, C.,Tontsch-Grunt, U.,Waizenegger, I.C.,Solca, F.,Bader, G.,Zoephel, A.,Treu, M.,Reiser, U.,Garin-Chesa, P.,Boehmelt, G.,Kraut, N.,Quant, J.,Adolf, G.R.
Pharmacological Profile of BI 847325, an Orally Bioavailable, ATP-Competitive Inhibitor of MEK and Aurora Kinases.
Mol.Cancer Ther., 15:2388-2398, 2016
Cited by
PubMed: 27496137
DOI: 10.1158/1535-7163.MCT-16-0066
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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