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European Journal of Biochemistry|May 1, 1994
(Rp)- and (Sp)-8-piperidino-adenosine 3',5'-(cyclic)thiophosphates discriminate completely between site A and B of the regulatory subunits of cAMP-dependent protein kinase type I and IID Ogreid, W Dostmann, H G Genieser, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|March 30, 2005
Effect of cAMP analogues on glomerular inulin space of isolated rats renal glomeruliM X P van Bemmelen, M Szczepańska-Konkel, B Jastorff, et al.
FEBS Letters|April 10, 1995
Ala335 is essential for high-affinity cAMP-binding of both sites A and B of cAMP-dependent protein kinase type IM Zorn, K E Fladmark, D Ogreid, et al.
The Journal of Physical Chemistry. B|November 28, 2006
Structure and bonding of the multifunctional amino acid L-DOPA on Au(110)M Weinhold, S Soubatch, R Temirov, et al.
Molecular Pharmacology|October 1, 1994
Membrane-permeant derivatives of cyclic AMP optimized for high potency, prolonged activity, or rapid reversibilityC Schultz, M Vajanaphanich, H G Genieser, et al.
FEMS Microbiology Letters|July 15, 1991
Kinetics and nucleotide specificity of a surface cAMP binding site in Dictyostelium discoideum, which is not down-regulated by cAMPM van Ments-Cohen, H G Genieser, B Jastorff, et al.
Biochemistry|July 29, 2000
8-Substituted cAMP analogues reveal marked differences in adaptability, hydrogen bonding, and charge accommodation between homologous binding sites (AI/AII and BI/BII) in cAMP kinase I and IIF Schwede, A Christensen, S Liauw, et al.
Biochemical Pharmacology|June 23, 1992
Analysis of the functional role of cGMP-dependent protein kinase in intact human platelets using a specific activator 8-para-chlorophenylthio-cGMPE Butt, C Nolte, S Schulz, et al.
The Journal of Biological Chemistry|January 25, 1986
Studies of cGMP analog specificity and function of the two intrasubunit binding sites of cGMP-dependent protein kinaseJ D Corbin, D Ogreid, J P Miller, et al.
The Journal of Biological Chemistry|June 25, 1990
Probing the cyclic nucleotide binding sites of cAMP-dependent protein kinases I and II with analogs of adenosine 3',5'-cyclic phosphorothioatesW R Dostmann, S S Taylor, H G Genieser, et al.
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