The stereochemical course of the reaction catalyzed by soluble bovine lung guanylate cyclase.
Open Access
- 1 June 1983
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 258 (11) , 6741-6745
- https://doi.org/10.1016/s0021-9258(18)32282-8
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Synthesis of adenosine 5′[(R)α-17O]triphosphateJournal of the Chemical Society, Chemical Communications, 1982
- Soluble guanylate cyclase purified from bovine lung contains heme and copperFEBS Letters, 1981
- Analysis of the chirality of [16O,17O,18O] phosphate esters by 31P nuclear magnetic resonance spectroscopyJournal of the Chemical Society, Perkin Transactions 1, 1981
- Guanylate cyclase in synaptosomal soluble fraction from rat brain: Possible involvement of free radical acceptor in endogenous activation mechanismsNeurochemistry International, 1981
- Oxygen chiral phosphodiesters. 2. Enzymic synthesis and configurational analysis of [.alpha.-18O]-2'-deoxyadenosine 5'-diphosphateJournal of the American Chemical Society, 1980
- Oxygen chiral phosphodiesters. 1. Synthesis and configurational analysis of cyclic [18O]-2'-deoxyadenosine 3',5'-monophosphateJournal of the American Chemical Society, 1980
- Phosphorothioate analogs of nucleotidesAccounts of Chemical Research, 1979
- Stereospecific synthesis of adenosine 3′,5′-(SP)- and -(RP)-cyclic phosphorothioates (cAMPS)Journal of the Chemical Society, Chemical Communications, 1979
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- Cyclic GMP Metabolism and Involvement in Biological RegulationAnnual Review of Biochemistry, 1977