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Protein Sci ; 8(12): 2697-704, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10631985

ABSTRACT

Direct thermodynamic and kinetic investigations of the binding of nucleotides to the nucleoside monophosphate (NMP) site of NMP kinases have not been possible so far because a spectroscopic probe was not available. By coupling a fluorescent N-methylanthraniloyl- (mant) group to the beta-phosphate of CDP via a butyl linker, a CDP analogue [(Pbeta)MABA-CDP] was obtained that still binds specifically to the NMP site of UmpKdicty, because the base and the ribose moieties, which are involved in specific interactions, are not modified. This allows the direct determination of binding constants for its substrates in competition experiments.


Subject(s)
Cytidine Diphosphate/analogs & derivatives , Cytidine Diphosphate/chemistry , Dictyostelium/chemistry , Fluorescent Dyes/chemistry , Nucleoside-Phosphate Kinase/chemistry , Pyrimidinones/chemistry , Adenosine Triphosphate/chemistry , Animals , Binding Sites , Cytidine Diphosphate/chemical synthesis , Fluorescent Dyes/chemical synthesis , Kinetics , Magnetic Resonance Spectroscopy , Spectrometry, Fluorescence
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