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Aplysia californica mediated cyclisation of novel 3'-modified NAD+ analogues: a role for hydrogen bonding in the recognition of cyclic adenosine 5'-diphosphate ribose.

Abstract:

Cyclic ADP-ribose mobilizes intracellular Ca2+ in a variety of cells. To elucidate the nature of the interaction between the C3' substituent of cADP-ribose and the cADPR receptor, three analogues of NAD+ modified in the adenosine ribase (xyloNAD+ 3'F-xyloNAD+ and 3'F-NAD+ were chemically synthesised from D-xylose and adenine starting materials. 3'F-NAD+ was readily converted to cyclic 3'F-ADP ribose by the action of the cyclase enzyme derived from the mollusc Aplysia californica. XyloNAD+ and...

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Publication status:
Published

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Publisher copy:
10.1016/j.bmc.2003.10.012

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
Journal:
Bioorganic and medicinal chemistry More from this journal
Volume:
12
Issue:
2
Pages:
475-487
Publication date:
2004-01-01
DOI:
EISSN:
1464-3391
ISSN:
0968-0896
Language:
English
Keywords:
Pubs id:
pubs:106151
UUID:
uuid:b760901b-08c0-4034-8c29-20ec3a4ecfb0
Local pid:
pubs:106151
Source identifiers:
106151
Deposit date:
2012-12-19

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