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5BYY

ERK5 IN COMPLEX WITH SMALL MOLECULE

Summary for 5BYY
Entry DOI10.2210/pdb5byy/pdb
DescriptorMitogen-activated protein kinase 7, 2-{[2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl]amino}-5,11-dimethyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one (3 entities in total)
Functional Keywordserk5 kinase, kinase inhibitor, proteros biostructures gmbh, transferase
Biological sourceHomo sapiens (Human)
Cellular locationCytoplasm: Q13164
Total number of polymer chains1
Total formula weight40087.15
Authors
Chen, H.,Tucker, J.,Wang, X.,Gavine, P.R.,Philips, C.,Augustin, M.A.,Schreiner, P.,Steinbacher, S.,Preston, M.,Ogg, D. (deposition date: 2015-06-11, release date: 2016-05-04, Last modification date: 2016-05-11)
Primary citationChen, H.,Tucker, J.,Wang, X.,Gavine, P.R.,Phillips, C.,Augustin, M.A.,Schreiner, P.,Steinbacher, S.,Preston, M.,Ogg, D.
Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site.
Acta Crystallogr D Struct Biol, 72:682-693, 2016
Cited by
PubMed: 27139631
DOI: 10.1107/S2059798316004502
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.79 Å)
Structure validation

218500

건을2024-04-17부터공개중

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