Two Hydrolase Resistant Analogues of Diadenosine 5′,5″′-P,P-Triphosphate for Studies with FHIT, The Human Fragile Histidine Triad Protein

The design and synthesis of analogues of diadenosine 5′,5″′-P,P-triphosphate that are resistant to pyrophosphate hydrolysis is described in relation to their rôle in signalling and tumorigenesis involving the Fhit protein, the human fragile histidine triad protein, which is a novel Ap3A binding/clea...

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Veröffentlicht in:Nucleosides & nucleotides 1998-01, Vol.17 (1-3), p.301-308
Hauptverfasser: Blackburn, G. Michael, Liu, Xiaohai, Rösler, Angelika, Brenner, Charles
Format: Artikel
Sprache:eng
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Zusammenfassung:The design and synthesis of analogues of diadenosine 5′,5″′-P,P-triphosphate that are resistant to pyrophosphate hydrolysis is described in relation to their rôle in signalling and tumorigenesis involving the Fhit protein, the human fragile histidine triad protein, which is a novel Ap3A binding/cleaving protein. Dedicated to the memory of Professor Tsujiaki Hata, friend and associate for many years, who himself held a close interest in diadenosine and diguanosine polyphosphates.
ISSN:0732-8311
1525-7770
DOI:10.1080/07328319808005178