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Ligands
Code Name Style Show Link
3FX (2r)-3-(cyclohexylamino)-2-hydroxypropane-1-sulfonic acid
3FY N-(2-{(4-bromophenyl)[(1-methyl-1h-imidazol-5-yl)methyl]amino}ethyl)-1-methyl-N-(2-methylbenzyl)-1h-imidazole-4-sulfonamide
FII [(3,7,11-trimethyl-dodeca-2,6,10-trienyloxycarbamoyl)-methyl]-phosphonic acid
SO4 Sulfate ion
ZN Zinc ion
Non-standard Residues
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Code : 3SFY   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : Cryptococcus neoformans protein farnesyltransferase in complex with FPT-II and ethylenediamine inhibitor 2
Release Data : 2011-08-03
Compound :
mol_id molecule chains
1 Cryptococcus neoformans protein farnesyltransferase alpha subunit A
mol_id molecule chains
2 Cryptococcus neoformans protein farnesyltransferase beta subunit B
Source :
mol_id organism_scientific expression_system
1 Cryptococcus neoformans  (taxid:235443) Escherichia coli  (taxid:562)
strain: H99
mol_id organism_scientific expression_system
2 Cryptococcus neoformans  (taxid:235443) Escherichia coli  (taxid:562)
strain: H99
Authors : Hast, M.A., Beese, L.S.
Keywords : prenyltransferase, protein farnesyltransferase, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.10 Å )
Citation :

Structures of Cryptococcus neoformans Protein Farnesyltransferase Reveal Strategies for Developing Inhibitors That Target Fungal Pathogens.

Hast, M.A.,Nichols, C.B.,Armstrong, S.M.  et al.
(2011)  J.Biol.Chem.  286 : 35149 - 35162

PubMed: 21816822
DOI: 10.1074/jbc.M111.250506