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4I5H

Crystal Structure of a Double Mutant Rat Erk2 Complexed With a Type II Quinazoline Inhibitor

Summary for 4I5H
Entry DOI10.2210/pdb4i5h/pdb
DescriptorMitogen-activated protein kinase 1, N-{3-[2-(cyclopropylamino)quinazolin-6-yl]-4-methylphenyl}-3-(trifluoromethyl)benzamide (3 entities in total)
Functional Keywordsmap kinase, dfg-out, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceRattus norvegicus (brown rat,rat,rats)
Cellular locationCytoplasm, cytoskeleton, spindle (By similarity): P63086
Total number of polymer chains1
Total formula weight41815.97
Authors
Hari, S.B.,Maly, D.J.,Merritt, E.A. (deposition date: 2012-11-28, release date: 2013-07-10, Last modification date: 2024-02-28)
Primary citationHari, S.B.,Merritt, E.A.,Maly, D.J.
Sequence determinants of a specific inactive protein kinase conformation.
Chem.Biol., 20:806-815, 2013
Cited by
PubMed: 23790491
DOI: 10.1016/j.chembiol.2013.05.005
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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