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4NEU

X-ray structure of Receptor Interacting Protein 1 (RIP1)kinase domain with a 1-aminoisoquinoline inhibitor

Summary for 4NEU
Entry DOI10.2210/pdb4neu/pdb
DescriptorReceptor-interacting serine/threonine-protein kinase 1, MAGNESIUM ION, 1-[4-(1-aminoisoquinolin-5-yl)phenyl]-3-(5-tert-butyl-1,2-oxazol-3-yl)urea, ... (4 entities in total)
Functional Keywordskinase, atp binding, phosphorylation, transferase
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: Q13546
Total number of polymer chains2
Total formula weight77245.26
Authors
Nolte, R.T.,Ward, P.,kahler, K.M.,Campobasso, N. (deposition date: 2013-10-30, release date: 2013-11-20, Last modification date: 2024-02-28)
Primary citationHarris, P.A.,Bandyopadhyay, D.,Berger, S.B.,Campobasso, N.,Capriotti, C.A.,Cox, J.A.,Dare, L.,Finger, J.N.,Hoffman, S.J.,Kahler, K.M.,Lehr, R.,Lich, J.D.,Nagilla, R.,Nolte, R.T.,Ouellette, M.T.,Pao, C.S.,Schaeffer, M.C.,Smallwood, A.,Sun, H.H.,Swift, B.A.,Totoritis, R.D.,Ward, P.,Marquis, R.W.,Bertin, J.,Gough, P.J.
Discovery of Small Molecule RIP1 Kinase Inhibitors for the Treatment of Pathologies Associated with Necroptosis.
ACS Med Chem Lett, 4:1238-1243, 2013
Cited by
PubMed: 24900635
DOI: 10.1021/ml400382p
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.57 Å)
Structure validation

218500

數據於2024-04-17公開中

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