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2IEJ

Human Protein Farnesyltransferase Complexed with Inhibitor Compound STN-48 And FPP Analog at 1.8A Resolution

Summary for 2IEJ
Entry DOI10.2210/pdb2iej/pdb
Related PRD IDPRD_900003
DescriptorProtein farnesyltransferase/geranylgeranyltransferase type I alpha subunit, Protein farnesyltransferase subunit beta, beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, ... (8 entities in total)
Functional Keywordsftase, farnesyltransferase, farnesyl transferase, caax, ras, cancer, tumor regression, stn-48, protein prenylation, lipid modification, plasmodium, falciparum, malaria, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight95284.20
Authors
Hast, M.A.,Beese, L.S. (deposition date: 2006-09-19, release date: 2007-01-23, Last modification date: 2024-02-21)
Primary citationEastman, R.T.,White, J.,Hucke, O.,Yokoyama, K.,Verlinde, C.L.,Hast, M.A.,Beese, L.S.,Gelb, M.H.,Rathod, P.K.,Van Voorhis, W.C.
Resistance mutations at the lipid substrate binding site of Plasmodium falciparum protein farnesyltransferase.
Mol.Biochem.Parasitol., 152:66-71, 2007
Cited by
PubMed: 17208314
DOI: 10.1016/j.molbiopara.2006.11.012
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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