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Two hydrolase resistant analogues of diadenosine 5',5"'-P1,P3-triphosphate for studies with Fhit, the human fragile histidine triad protein
Journal article

Two hydrolase resistant analogues of diadenosine 5',5"'-P1,P3-triphosphate for studies with Fhit, the human fragile histidine triad protein

G Michael Blackburn, Xiaohai Liu, Angelika Rösler and Charles Brenner
Nucleosides & nucleotides, Vol.17(1-3), pp.301-308
01/1998
DOI: 10.1080/07328319808005178
PMCID: PMC2556045
PMID: 9708352

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Abstract

The design and synthesis of analogues of diadenosine 5',5"'-P1,P3-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.
DNA-Binding Proteins - metabolism Hydrolysis Proteins - metabolism Stereoisomerism Humans Neoplasm Proteins Binding Sites - physiology Acid Anhydride Hydrolases - metabolism Molecular Structure Dinucleoside Phosphates - chemistry Polyphosphates - chemical synthesis

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