-
2
-
-
0034725748
-
Soluble adenylyl cyclase as an evolutionarily conserved bicarbonate sensor
-
DOI 10.1126/science.289.5479.625
-
Chen Y, Cann MJ, Litvin TN, Iourgenko V, Sinclair ML, Levin LR, and Buck J (2000) Soluble adenylyl cyclase as an evolutionarily conserved bicarbonate sensor. Science 289:625-628. (Pubitemid 30622067)
-
(2000)
Science
, vol.289
, Issue.5479
, pp. 625-628
-
-
Chen, Y.1
Cann, M.J.2
Litvin, T.N.3
Iourgenko, V.4
Sinclair, M.L.5
Levin, L.R.6
Buck, J.7
-
3
-
-
0033835813
-
Tissue specificity and physiological relevance of various isoforms of adenylyl cyclase
-
Defer N, Best-Belpomme M, and Hanoune J (2000) Tissue specificity and physiological relevance of various isoforms of adenylyl cyclase. Am J Physiol Renal Physiol 279:F400-F416.
-
(2000)
Am J Physiol Renal Physiol
, vol.279
-
-
Defer, N.1
Best-Belpomme, M.2
Hanoune, J.3
-
5
-
-
28244461565
-
Differential interactions of G-proteins and adenylyl cyclase with nucleoside 5′-triphosphates, nucleoside 5′-[γ-thio] triphosphates and nucleoside 5′-[β,γ-imido]triphosphates
-
DOI 10.1016/j.bcp.2005.10.006, PII S0006295205006556
-
Gille A, Guo J, Mou TC, Doughty MB, Lushington GH, and Seifert R (2005) Differential interactions of G-proteins and adenylyl cyclase with nucleoside 5′-triphosphates, nucleoside 5′-[γ-thio]triphosphates and nucleoside 5′-[β,γ-imido]triphosphates. Biochem Pharmacol 71:89-97. (Pubitemid 41713530)
-
(2005)
Biochemical Pharmacology
, vol.71
, Issue.1-2
, pp. 89-97
-
-
Gille, A.1
Guo, J.2
Mou, T.-C.3
Doughty, M.B.4
Lushington, G.H.5
Seifert, R.6
-
7
-
-
2442506761
-
Differential Inhibition of Adenylyl Cyclase Isoforms and Soluble Guanylyl Cyclase by Purine and Pyrimidine Nucleotides
-
DOI 10.1074/jbc.M312560200
-
Gille A, Lushington GH, Mou TC, Doughty MB, Johnson RA, and Seifert R (2004) Differential inhibition of adenylyl cyclase isoforms and soluble guanylyl cyclase by purine and pyrimidine nucleotides. J Biol Chem 279:19955-19969. (Pubitemid 38623438)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.19
, pp. 19955-19969
-
-
Gille, A.1
Lushington, G.H.2
Mou, T.-C.3
Doughty, M.B.4
Johnson, R.A.5
Seifert, R.6
-
8
-
-
0037630420
-
2′(3′)-O-(N-methylanthraniloyl)-substituted GTP analogs: A novel class of potent competitive adenylyl cyclase inhibitors
-
DOI 10.1074/jbc.M211292200
-
Gille A and Seifert R (2003a) 2′(3′)-O-(N-Methylanthraniloyl) -substituted GTP analogs: a novel class of potent competitive adenylyl cyclase inhibitors. J Biol Chem 278:12672-12679. (Pubitemid 36800027)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.15
, pp. 12672-12679
-
-
Gille, A.1
Seifert, R.2
-
10
-
-
34548315751
-
Molecular analysis of the interaction of Bordetella pertussis adenylyl cyclase with fluorescent nucleotides
-
DOI 10.1124/mol.107.034413
-
Göttle M, Dove S, Steindel P, Shen Y, Tang WJ, Geduhn J, König B, and Seifert R (2007) Molecular analysis of the interaction of Bordetella pertussis adenylyl cyclase with fluorescent nucleotides. Mol Pharmacol 72:526-535. (Pubitemid 47347287)
-
(2007)
Molecular Pharmacology
, vol.72
, Issue.3
, pp. 526-535
-
-
Gottle, M.1
Dove, S.2
Steindel, P.3
Shen, Y.4
Tang, W.-J.5
Geduhn, J.6
Konig, B.7
Seifert, R.8
-
11
-
-
66749133607
-
Characterization of mouse heart adenylyl cyclase
-
Göttle M, Geduhn J, König B, Gille A, Höcherl K, and Seifert R (2009) Characterization of mouse heart adenylyl cyclase. J Pharmacol Exp Ther 329:1156-1165.
-
(2009)
J Pharmacol Exp Ther
, vol.329
, pp. 1156-1165
-
-
Göttle, M.1
Geduhn, J.2
König, B.3
Gille, A.4
Höcherl, K.5
Seifert, R.6
-
12
-
-
0041323078
-
Fluorescent and colored trinitrophenylated analogs of ATP and GTP
-
Hiratsuka T (2003) Fluorescent and colored trinitrophenylated analogs of ATP and GTP. Eur J Biochem 270:3479-3485.
-
(2003)
Eur J Biochem
, vol.270
, pp. 3479-3485
-
-
Hiratsuka, T.1
-
13
-
-
0020674810
-
New ribose-modified fluorescent analogs of adenine and guanine nucleotides available as substrates for various enzymes
-
Hiratsuka T (1983) New ribose-modified fluorescent analogs of adenine and guanine nucleotides available as substrates for various enzymes. Biochim Biophys Acta 742:496-508.
-
(1983)
Biochim Biophys Acta
, vol.742
, pp. 496-508
-
-
Hiratsuka, T.1
-
14
-
-
4644330950
-
Direct inhibition of type 5 adenylyl cyclase prevents myocardial apoptosis without functional deterioration
-
DOI 10.1074/jbc.M314238200
-
Iwatsubo K, Minamisawa S, Tsunematsu T, Nakagome M, Toya Y, Tomlinson JE, Umemura S, Scarborough RM, Levy DE, and Ishikawa Y (2004) Direct inhibition of type 5 adenylyl cyclase prevents myocardial apoptosis without functional deterioration. J Biol Chem 279:40938-40945. (Pubitemid 39287693)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.39
, pp. 40938-40945
-
-
Iwatsubo, K.1
Minamisawa, S.2
Tsunematsu, T.3
Nakagome, M.4
Toya, Y.5
Tomlinson, J.E.6
Umemura, S.7
Scarborough, R.M.8
Levy, D.E.9
Ishikawa, Y.10
-
15
-
-
0030971247
-
Fluorescent nucleotide analogs: Synthesis and applications
-
DOI 10.1016/S0076-6879(97)78020-0
-
Jameson DM and Eccleston JF (1997) Fluorescent nucleotide analogs: synthesis and applications. Methods Enzymol 278:363-390. (Pubitemid 27229929)
-
(1997)
Methods in Enzymology
, vol.278
, pp. 363-390
-
-
Jameson, D.M.1
Eccleston, J.F.2
-
16
-
-
4243049145
-
Nitric oxide-sensitive guanylyl cyclase: Structure and regulation
-
DOI 10.1016/j.neuint.2004.03.011, PII S0197018604000592
-
Koesling D, Russwurm M, Mergia E, Mullershausen F, and Friebe A (2004) Nitric oxide-sensitive guanylyl cyclase: structure and regulation. Neurochem Int 45:813-819. (Pubitemid 39108053)
-
(2004)
Neurochemistry International
, vol.45
, Issue.6
, pp. 813-819
-
-
Koesling, D.1
Russwurm, M.2
Mergia, E.3
Mullershausen, F.4
Friebe, A.5
-
17
-
-
1842728354
-
Pro-nucleotide Inhibitors of Adenylyl Cyclases in Intact Cells
-
DOI 10.1074/jbc.M309535200
-
Laux WH, Pande P, Shoshani I, Gao J, Boudou-Vivet V, Gosselin G, and Johnson RA (2004) Pro-nucleotide inhibitors of adenylyl cyclase in intact cells. J Biol Chem 279:13317-13332. (Pubitemid 38468854)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.14
, pp. 13317-13332
-
-
Laux, W.H.G.1
Pande, P.2
Shoshani, I.3
Gao, J.4
Boudou-Vivet, V.5
Gosselin, G.6
Johnson, R.A.7
-
18
-
-
0034922158
-
sαS: Consequences for receptor-coupling and adenylyl cyclase activation
-
sαS: consequences for receptor-coupling and adenylyl cyclase activation. J Neurochem 78:325-338.
-
(2001)
J Neurochem
, vol.78
, pp. 325-338
-
-
Liu, H.Y.1
Wenzel-Seifert, K.2
Seifert, R.3
-
19
-
-
14844299755
-
Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-triphosphate
-
DOI 10.1074/jbc.M409076200
-
Mou TC, Gille A, Fancy DA, Seifert R, and Sprang SR (2005) Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-triphosphate. J Biol Chem 280:7253-7261. (Pubitemid 40341283)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.8
, pp. 7253-7261
-
-
Mou, T.-C.1
Gille, A.2
Fancy, D.A.3
Seifert, R.4
Sprang, S.R.5
-
20
-
-
33747624168
-
Broad specificity of mammalian adenylyl cyclase for interaction with 2′,3′-substituted purine- And pyrimidine nucleotide inhibitors
-
DOI 10.1124/mol.106.026427
-
Mou TC, Gille A, Suryanarayana S, Richter M, Seifert R, and Sprang SR (2006) Broad specificity of mammalian adenylyl cyclase for interaction with 2′,3′-substituted purine- and pyrimidine nucleotide inhibitors. Mol Pharmacol 70:878-886. (Pubitemid 44268445)
-
(2006)
Molecular Pharmacology
, vol.70
, Issue.3
, pp. 878-886
-
-
Mou, T.-C.1
Gille, A.2
Suryanarayana, S.3
Richter, M.4
Seifert, R.5
Sprang, S.R.6
-
21
-
-
0022449218
-
Extraction, purification, identification and metabolism of 3′,5′-cyclic UMP, 3′,5′-cyclic IMP and 3′,5′-cyclic dTMP from rat tissues
-
Newton RP, Kingston EE, Hakeem NA, Salih SG, Beynon JH, and Moyse CD (1986) Extraction, purification, identification and metabolism of 3′,5′-cyclic UMP, 3′,5′-cyclic IMP and 3′,5′-cyclic dTMP from rat tissues. Biochem J 236:431-439.
-
(1986)
Biochem J
, vol.236
, pp. 431-439
-
-
Newton, R.P.1
Kingston, E.E.2
Hakeem, N.A.3
Salih, S.G.4
Beynon, J.H.5
Moyse, C.D.6
-
22
-
-
0021233449
-
Extraction, purification and identification of cytidine 3′,5′-cyclic monophosphate from rat tissues
-
Newton RP, Salih SG, Salvage BJ, and Kingston EE (1984) Extraction, purification and identification of cytidine 3′,5′-cyclic monophosphate from rat tissues. Biochem J 221:665-673.
-
(1984)
Biochem J
, vol.221
, pp. 665-673
-
-
Newton, R.P.1
Salih, S.G.2
Salvage, B.J.3
Kingston, E.E.4
-
23
-
-
0025141725
-
Cytidylate cyclase: Development of assay and determination of kinetic properties of a cytidine 3′,5′-cyclic monophosphate-synthesizing enzyme
-
Newton RP, Salvage BJ, and Hakeem NA (1990) Cytidylate cyclase: development of assay and determination of kinetic properties of a cytidine 3′,5′-cyclic monophosphate-synthesizing enzyme. Biochem J 265:581-586.
-
(1990)
Biochem J
, vol.265
, pp. 581-586
-
-
Newton, R.P.1
Salvage, B.J.2
Hakeem, N.A.3
-
24
-
-
67349241188
-
Differential interactions of the catalytic subunits of adenylyl cyclase with forskolin analogs
-
Pinto C, Hübner M, Gille A, Richter M, Mou TC, Sprang SR, and Seifert R (2009) Differential interactions of the catalytic subunits of adenylyl cyclase with forskolin analogs. Biochem Pharmacol 78:62-69.
-
(2009)
Biochem Pharmacol
, vol.78
, pp. 62-69
-
-
Pinto, C.1
Hübner, M.2
Gille, A.3
Richter, M.4
Mou, T.C.5
Sprang, S.R.6
Seifert, R.7
-
25
-
-
41149107453
-
Activation and inhibition of adenylyl cyclase isoforms by forskolin analogs
-
Pinto C, Papa D, Hübner M, Mou TC, Lushington GH, and Seifert R (2008) Activation and inhibition of adenylyl cyclase isoforms by forskolin analogs. J Pharmacol Exp Ther 325:27-36.
-
(2008)
J Pharmacol Exp Ther
, vol.325
, pp. 27-36
-
-
Pinto, C.1
Papa, D.2
Hübner, M.3
Mou, T.C.4
Lushington, G.H.5
Seifert, R.6
-
26
-
-
34247216741
-
Functional adenylyl cyclase inhibition in murine cardiomyocytes by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-[′-thio] triphosphate
-
DOI 10.1124/jpet.106.118422
-
Rottlaender D, Matthes J, Vatner SF, Seifert R, and Herzig S (2007) Functional adenylyl cyclase inhibition in murine cardiomyocytes by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-[γ-thio] triphosphate. J Pharmacol Exp Ther 321:608-615. (Pubitemid 46624491)
-
(2007)
Journal of Pharmacology and Experimental Therapeutics
, vol.321
, Issue.2
, pp. 608-615
-
-
Rottlaender, D.1
Matthes, J.2
Vatner, S.F.3
Seifert, R.4
Herzig, S.5
-
27
-
-
49449098340
-
Structure-based development of novel adenylyl cyclase inhibitors
-
Schlicker C, Rauch A, Hess KC, Kachholz B, Levin LR, Buck J, and Steegborn C (2008) Structure-based development of novel adenylyl cyclase inhibitors. J Med Chem 51:4456-4464.
-
(2008)
J Med Chem
, vol.51
, pp. 4456-4464
-
-
Schlicker, C.1
Rauch, A.2
Hess, K.C.3
Kachholz, B.4
Levin, L.R.5
Buck, J.6
Steegborn, C.7
-
28
-
-
61749100199
-
NO- And haem-independent soluble guanylate cyclase activators
-
Schmidt HH, Schmidt PM, and Stasch JP (2009) NO- and haem-independent soluble guanylate cyclase activators. Handb Exp Pharmacol 191:309-339.
-
(2009)
Handb Exp Pharmacol
, vol.191
, pp. 309-339
-
-
Schmidt, H.H.1
Schmidt, P.M.2
Stasch, J.P.3
-
31
-
-
0032568930
-
Exchange of substrate and inhibitor specificities between adenylyl and guanylyl cyclases
-
DOI 10.1074/jbc.273.26.16332
-
Sunahara RK, Beuve A, Tesmer JJ, Sprang SR, Garbers DL, and Gilman AG (1998) Exchange of substrate and inhibitor specificities between adenylyl and guanylyl cyclases. J Biol Chem 273:16332-16338. (Pubitemid 28311412)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.26
, pp. 16332-16338
-
-
Sunahara, R.K.1
Beuve, A.2
Tesmer, J.J.G.3
Sprang, S.R.4
Garbers, D.L.5
Gilman, A.G.6
-
32
-
-
0141541343
-
Isoforms of mammalian adenylyl cyclase. Multiplicities of signaling
-
Sunahara RK and Taussig R (2002) Isoforms of mammalian adenylyl cyclase. Multiplicities of signaling. Mol Interv 2:168-184.
-
(2002)
Mol Interv
, vol.2
, pp. 168-184
-
-
Sunahara, R.K.1
Taussig, R.2
-
33
-
-
62149085232
-
Molecular analysis of the interaction of anthrax adenylyl cyclase toxin, edema factor, with 2′(3′)-O-(N-(methyl)anthraniloyl)-substituted purine and pyrimidine nucleotides
-
Taha HM, Schmidt J, Göttle M, Suryanarayana S, Shen Y, Tang WJ, Gille A, Geduhn J, König B, Dove S, et al. (2009) Molecular analysis of the interaction of anthrax adenylyl cyclase toxin, edema factor, with 2′(3′)-O-(N-(methyl)anthraniloyl)-substituted purine and pyrimidine nucleotides. Mol Pharmacol 75:693-703.
-
(2009)
Mol Pharmacol
, vol.75
, pp. 693-703
-
-
Taha, H.M.1
Schmidt, J.2
Göttle, M.3
Suryanarayana, S.4
Shen, Y.5
Tang, W.J.6
Gille, A.7
Geduhn, J.8
König, B.9
Dove, S.10
-
34
-
-
0034727680
-
Molecular basis for P-site inhibition of adenylyl cyclase
-
Tesmer JJ, Dessauer CW, Sunahara RK, Murray LD, Johnson RA, Gilman AG, and Sprang SR (2000) Molecular basis for P-site inhibition of adenylyl cyclase. Biochemistry 39:14464-14471.
-
(2000)
Biochemistry
, vol.39
, pp. 14464-14471
-
-
Tesmer, J.J.1
Dessauer, C.W.2
Sunahara, R.K.3
Murray, L.D.4
Johnson, R.A.5
Gilman, A.G.6
Sprang, S.R.7
-
38
-
-
34447528668
-
Type 5 Adenylyl Cyclase Disruption Increases Longevity and Protects Against Stress
-
DOI 10.1016/j.cell.2007.05.038, PII S0092867407006770
-
Yan L, Vatner DE, O'Connor JP, Ivessa A, Ge H, Chen W, Hirotani S, Ishikawa Y, Sadoshima J, and Vatner SF (2007) Type 5 adenylyl cyclase disruption increases longevity and protects against stress. Cell 130:247-258. (Pubitemid 47081133)
-
(2007)
Cell
, vol.130
, Issue.2
, pp. 247-258
-
-
Yan, L.1
Vatner, D.E.2
O'Connor, J.P.3
Ivessa, A.4
Ge, H.5
Chen, W.6
Hirotani, S.7
Ishikawa, Y.8
Sadoshima, J.9
Vatner, S.F.10
|