Deoxyadenosine phosphates formation

ATP -I- 2 -deoxynucleoside = ADP + 2 -deoxynucleoside 5 -phosphate (<1>, compulsory ordered steady-state reaction mechanism with formation of a ternary complex with the phosphate donor and acceptor [2] the enzyme from embryonic cells of Drosophila melanogaster differs from other deoxynucleoside kinases [EC 2.7.1.76 (deoxyadenosine kinase) and EC 2.7.1.113 (deoxyguanosine kinase)] in its broad specificity for all four common deoxynucleosides)... 

Kornberg s work on the biosynthesis of deoxyribonucleic acid has shown that enzymes in Escherichia coli extracts catalyze the formation of the 5-triphosphates of 2-deoxyadenosine, 2-deoxyguanosine, 2-deoxycyti-dine, and thymidine from the corresponding monophosphates in the presence of adenosine 5-triphosphate, but fail to catalyze phosphorylation of deoxyuridine 5-phosphate this finding could explain why uracil is not a constituent of deoxyribonucleic acid. 

Pyrolysis of nucleic acids compared to ion fragments formation from adenosine-5 -phosphate and 2-deoxyadenosine-5 -phosphate. 

Recently, evidence has emerged that in some DNAs with unusually regular base sequences, the sugar-phosphate backbone may adopt a very different conformation from that of the regular right-handed helix of R-DNA. This has been most clearly demonstrated with polydeoxyribonucleotides with a simple alternating sequence of two bases. Poly(dA-dT), in which deoxyadenosine alternates with deoxythymidine in each strand so that duplex formation is possible by the usual complementary base... 

Two groups have reported the synthesis of compounds of type (139) as potential models for ring-opening reactions of cyclic AMP. These studies included cases where the dioxaphosphorinane ring was both apical-equatorial and diequatorial, and conformations were studied by n.m.r.i98,i99 xhe predominant formation of 3 -monophosphates in the base-catalysed hydrolysis of nucleoside 3, 5 -cyclic phosphates has been interpreted in terms of the lone pair orientation effect, which may decrease the energy of the transition state for P-O bond-breaking.200 Conformational studies have been carried out on the diastereomers of adenosine cyclic 3 ,5 -phosphorothioate, where chair conformations predominate, and for the / p-isomer of deoxyadenosine cyclic phosphoranilidate, where a chair-twist equilibrium... 

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