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TitleDesign and Synthesis of Active Site Inhibitors of the Human Farnesyl Pyrophosphate Synthase: Apoptosis and Inhibition of ERK Phosphorylation in Multiple Myeloma Cells.
Journal, issue, pagesJ. Med. Chem., Vol. 55, Page 3201-3215, Year 2012
Publish dateJan 20, 2012 (structure data deposition date)
AuthorsLin, Y.S. / Park, J. / De Schutter, J.W. / Huang, X.F. / Berghuis, A.M. / Sebag, M. / Tsantrizos, Y.S.
External linksJ. Med. Chem. / PubMed:22390415
MethodsX-ray diffraction
Resolution1.85 Å
Structure data

PDB-4dem:
Crystal structure of human FPPS in complex with YS_04_70
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

Chemicals

ChemComp-YS4:
[({4-[4-(propan-2-yloxy)phenyl]pyridin-2-yl}amino)methanediyl]bis(phosphonic acid)

ChemComp-MG:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / MEVALONATE PATHWAY / ISOPRENE BIOSYNTHESIS / CHOLESTEROL BIOSYNTHESIS / BISPHOSPHONATE / TRANSFERASE / TRANSFERASE-TRANSFERASE INHIBITOR complex

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