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3L8X

P38 alpha kinase complexed with a pyrazolo-pyrimidine based inhibitor

Replaces:  3CG2
Summary for 3L8X
Entry DOI10.2210/pdb3l8x/pdb
DescriptorMitogen-activated protein kinase 14, N,4-dimethyl-3-[(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzamide (3 entities in total)
Functional Keywordsp38 map kinase, serine/threonine-protein kinase, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight42463.40
Authors
Sack, J.S. (deposition date: 2010-01-04, release date: 2010-03-02, Last modification date: 2024-02-21)
Primary citationDas, J.,Moquin, R.V.,Pitt, S.,Zhang, R.,Shen, D.R.,Mcintyre, K.W.,Gillooly, K.,Doweyko, A.M.,Sack, J.S.,Zhang, H.,Kiefer, S.E.,Kish, K.,Mckinnon, M.,Barrish, J.C.,Dodd, J.H.,Schieven, G.L.,Leftheris, K.
Pyrazolo-Pyrimidines: A Novel Heterocyclic Scaffold for Potent and Selective P38 Alpha Inhibitors.
Bioorg.Med.Chem.Lett., 18:2652-, 2008
Cited by
PubMed: 18359226
DOI: 10.1016/J.BMCL.2008.03.019
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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