Results 161 to 170 of about 3,470 (173)
Some of the next articles are maybe not open access.

S-Adenosylhomocysteinase: mechanism of reversible and irreversible inactivation by ATP, cAMP, and 2'-deoxyadenosine

Biochemistry, 1986
Homogeneous S-adenosylhomocysteinase (AdoHcyase) from rat liver is a tetrameric enzyme that contains four molecules of tightly bound NAD per mole of enzyme. We report here that incubation of the rat liver enzyme with ATP, Mg2+, and KCl leads to conversion of the active enzyme to an inactive form with release of all enzyme-bound NAD which can be ...
G, de la Haba   +5 more
openaire   +2 more sources

Adenosylhomocysteinase and adenosine nucleosidase activities in Lupinus luteus cotyledons during seed formation and germination

Planta, 1978
The activities of adenosylhomocysteinase (EC 3.3.1.1) and adenosine nucleosidase (EC 3.2.2.7) were assayed in extracts from yellow lupin (Lupinus luteus L.) cotyledons at different stages of seed formation and seedling development. Adenosylhomocysteinase activity was demonstrated in all the cotyledon extracts examined. Its lowest level was found in the
A, Guranowski, J, Pawełkiewicz
openaire   +2 more sources

A study on the sequestration of adenosine and its conversion to adenine by the cyclic AMP-adenosine binding proteins/S-adenosylhomocysteinase from mouse liver

Biochimica et Biophysica Acta (BBA) - General Subjects, 1979
Abstract A fraction of adenosine bound to the cyclic AMP-adenosine binding protein/ S-adenosylhomocysteinase from mouse liver is almost instantaneously converted to adenine. The conversion ratio, defined ad the concentration of adenine divided by the sum of the concentrations of adenine and adenosine, and the sequestration of adenosine, determined as
J, Saebø, P M, Ueland
openaire   +2 more sources

Studies on the Chemical Synthesis of Potential Antimetabolites. 32.1Synthesis of β-D-Pentofuranosyldeazaadenines as Candidate Inhibitors forS-Adenosylhomocysteinases and Methyltransferases

Nucleosides and Nucleotides, 1982
Abstract 9-β-D-Arabinofuranosyldeazaadenines [1-deaza-araA (4a) and 3-deaza-araA (4b)] were prepared from 6-chloro-β-D-ribofuranosyl-1- (6a) and -3-deazapurine (6b), respectively. Synthesis of 2′-deoxy-1-deaza-adenosine (5a) from 1-deazaadenosine (6c) is also described.
Tomokazu Sugawara   +3 more
openaire   +1 more source

Studies on the Chemical Synthesis of Potential Antimetabolites. 35.1Synthesis of 2-Chloro-1-deazaadenosine and 2-Chloro-1-deazainosine as Candidate Inhibitors forS-Adenosylhomocysteinases and Methyltransferases

Nucleosides and Nucleotides, 1983
Abstract The syntheses of 2-chloro-1-deazaadenosine (2) and 2-chloro-1-deazainosine (3) are described. Conversion of 7-ribosylated 6-chloro-1-deazapurine 3-oxide to the desired 2,6-disubstituted 9-ribosyl-1-deazapurines was effected by a series of reactions involving “deoxygenative chlorination” and transglycosylation in satisfactory yields.
Tokuo Itoh   +3 more
openaire   +1 more source

The Centrality of S-Adenosylhomocysteinase in the Regulation of the Biological Utilization of S-Adenosylmethionine

1986
S-Adenosylhomocysteine (AdoHcy), first isolated as one of the products of transmethylation reactions from S-adenosylmethionine (AdoMet) (Cantoni & Scarano, 1954) has been shown to be a competitive inhibitor of all methyltransferases. This was first shown by Gibson et al.
openaire   +1 more source

Interaction of 9-beta-D-arabinofuranosyladenine, 9-beta-D-arabinofuranosyladenine 5'-monophosphate, and 9-beta-D-arabinofuranosyladenine 5'-triphosphate with S-adenosylhomocysteinase.

Cancer research, 1981
9-beta-D-Arabinofuranosyladenine (ara-A), 9-beta-D-arabinofuranosyladenine 5'-monophosphate, and 9-beta-D-arabinofuranosyladenine 5'-triphosphate competitively inhibit both the synthesis and hydrolysis of S-adenosylhomocysteine catalyzed by S-adenosylhomocysteinase [S-adenosylhomocysteine hydrolase (EC 3.3.1.1)] from mouse liver, and the inhibitor ...
S, Helland, P M, Ueland
openaire   +1 more source

Home - About - Disclaimer - Privacy