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3E34

Protein farnesyltransferase complexed with FPP and ethylenediamine-scaffold inhibitor 10

Summary for 3E34
Entry DOI10.2210/pdb3e34/pdb
Related1D8D 1KZO 1KZP 1SA4 1SA5 2IEJ 3E30 3E32 3E33 3E37
DescriptorProtein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha, Protein farnesyltransferase subunit beta, ZINC ION, ... (6 entities in total)
Functional Keywordsftase, protein farnesyltransferase, farnesyltransferase, malaria, plasmodium, falciparum, antimalarial, ethylenediamine, prenyltransferase, transferase, metal-binding, phosphoprotein, zinc
Biological sourceRattus norvegicus (rat)
More
Total number of polymer chains2
Total formula weight94009.07
Authors
Hast, M.A.,Beese, L.S. (deposition date: 2008-08-06, release date: 2009-03-10, Last modification date: 2024-02-21)
Primary citationHast, M.A.,Fletcher, S.,Cummings, C.G.,Pusateri, E.E.,Blaskovich, M.A.,Rivas, K.,Gelb, M.H.,Van Voorhis, W.C.,Sebti, S.M.,Hamilton, A.D.,Beese, L.S.
Structural basis for binding and selectivity of antimalarial and anticancer ethylenediamine inhibitors to protein farnesyltransferase.
Chem.Biol., 16:181-192, 2009
Cited by
PubMed: 19246009
DOI: 10.1016/j.chembiol.2009.01.014
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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