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Characterization Of The Active Site And Insight Into The Binding Mode Of The Anti-Angiogenesis Agent Fumagillin To The Manganese(Ii)-Loaded Methionyl Aminopeptidase From Escherichia Coli, Ventris D'Souza, Robert Brown, Brian Bennett, Richard Holz
Characterization Of The Active Site And Insight Into The Binding Mode Of The Anti-Angiogenesis Agent Fumagillin To The Manganese(Ii)-Loaded Methionyl Aminopeptidase From Escherichia Coli, Ventris D'Souza, Robert Brown, Brian Bennett, Richard Holz
Richard C. Holz
EPR spectra were recorded for methionine aminopeptidase from Escherichia coli (EcMetAP-I) samples (~2.5 mM) to which one and two equivalents of Mn(II) were added (the latter is referred to as [MnMn(EcMetAP-I)]). The spectra for each sample were indistinguishable except that the spectrum of [MnMn(EcMetAP-I)] was twice as intense. The EPR spectrum of [MnMn(EcMetAP-I)] exhibited the characteristic six-line g≈2 EPR signal of mononuclear Mn(II) with A av(55Mn)=9.3 mT (93 G) and exhibited Curie-law temperature dependence. This signal is typical of Mn(II) in a ligand sphere comprising oxygen and/or nitrogen …