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4D9T

Rsk2 C-terminal Kinase Domain with inhibitor (E)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate

Summary for 4D9T
Entry DOI10.2210/pdb4d9t/pdb
Related4D9U
DescriptorRibosomal protein S6 kinase alpha-3, methyl (2S)-3-{4-amino-7-[(1E)-3-hydroxyprop-1-en-1-yl]-5-(4-methylphenyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl}-2-cyanopropanoate, SODIUM ION, ... (4 entities in total)
Functional Keywordskinase, inhibitor, reversible, thiol, phosphorylation, migration, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationNucleus (By similarity): P51812
Total number of polymer chains1
Total formula weight38893.34
Authors
Serafimova, I.M.,Pufall, M.A.,Krishnan, S.,Duda, K.,Cohen, M.S.,Maglathlin, R.L.,McFarland, J.M.,Miller, R.M.,Frodin, M.,Taunton, J. (deposition date: 2012-01-12, release date: 2012-04-25, Last modification date: 2012-05-16)
Primary citationSerafimova, I.M.,Pufall, M.A.,Krishnan, S.,Duda, K.,Cohen, M.S.,Maglathlin, R.L.,McFarland, J.M.,Miller, R.M.,Frodin, M.,Taunton, J.
Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles.
Nat.Chem.Biol., 8:471-476, 2012
Cited by
PubMed: 22466421
DOI: 10.1038/nchembio.925
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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