1sa5

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[[Image:1sa5.gif|left|200px]]
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{{STRUCTURE_1sa5| PDB=1sa5 | SCENE= }}
{{STRUCTURE_1sa5| PDB=1sa5 | SCENE= }}
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'''Rat protein farnesyltransferase complexed with FPP and BMS-214662'''
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===Rat protein farnesyltransferase complexed with FPP and BMS-214662===
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==Overview==
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The search for new cancer therapeutics has identified protein farnesyltransferase (FTase) as a promising drug target. This enzyme attaches isoprenoid lipids to signal transduction proteins involved in growth and differentiation. The two FTase inhibitors (FTIs), R115777 (tipifarnib/Zarnestra) and BMS-214662, have undergone evaluation as cancer therapeutics in phase I and II clinical trials. R115777 has been evaluated in phase III clinical trials and shows indications for the treatment of blood and breast malignancies. Here we present crystal structures of R115777 and BMS-214662 complexed with mammalian FTase. These structures illustrate the molecular mechanism of inhibition and selectivity toward FTase over the related enzyme, protein geranylgeranyltransferase type I (GGTase-I). These results, combined with previous biochemical and structural analyses, identify features of FTase that could be exploited to modulate inhibitor potency and specificity and should aid in the continued development of FTIs as therapeutics for the treatment of cancer and parasitic infections.
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(as it appears on PubMed at http://www.pubmed.gov), where 15170324 is the PubMed ID number.
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{{ABSTRACT_PUBMED_15170324}}
==About this Structure==
==About this Structure==
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Revision as of 21:22, 28 July 2008

Image:1sa5.png

Template:STRUCTURE 1sa5

Rat protein farnesyltransferase complexed with FPP and BMS-214662

Template:ABSTRACT PUBMED 15170324

About this Structure

1SA5 is a Protein complex structure of sequences from Rattus norvegicus. Full crystallographic information is available from OCA.

Reference

Crystal structures of the anticancer clinical candidates R115777 (Tipifarnib) and BMS-214662 complexed with protein farnesyltransferase suggest a mechanism of FTI selectivity., Reid TS, Beese LS, Biochemistry. 2004 Jun 8;43(22):6877-84. PMID:15170324

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