Utilizing a dinuclear iron center tyrosyl radical cofactor, ribonucleoside diphosphate reductase (RNR) from E. coli catalyzes the conversion of nucleoside diphosphates to deoxynucleoside diphosphates. 2'-(E)-Fluromethylene-2'-deoxycytidine 5'-diphosphate (FMCDP) has recently been shown to be a near stoichiometric mechanism based inhibitor for this enzyme. Loss of the essential tyrosyl radical and formation of a new nucleotide based radical accompany inactivation. In order to gain insight into the structure of this radical, [6'-13C]-FMCDP has been synthesized, and the EPR spectrum of the radical resulting from its incubation with RDPR has been resolved. Simulation of the resulting spectrum provides unambiguous evidence that this new radical is allylic in nature, and is derived from H0133'-hydrogen atom abstraction mediated by RDPR.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR002583-13S1
Application #
6121172
Study Section
Project Start
1998-05-05
Project End
2000-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
13
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
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