-
1
-
-
68149136447
-
Sildenafil is a strong activator of mammalian carbonic anhydrase isoforms I-XIV
-
Abdulkadir Coban T, Beydemir S, Gucin I, Ekinci D, Innocenti A, Vullo D, Supuran CT (2009) Sildenafil is a strong activator of mammalian carbonic anhydrase isoforms I-XIV. Bioorg Med Chem 17:5791-5795
-
(2009)
Bioorg Med Chem
, vol.17
, pp. 5791-5795
-
-
Abdulkadir Coban, T.1
Beydemir, S.2
Gucin, I.3
Ekinci, D.4
Innocenti, A.5
Vullo, D.6
Supuran, C.T.7
-
2
-
-
0028839684
-
Activationand selective Inhibitionof acyclic AMP- specificphosphodiesterase PDE4D3
-
Alvarez R, Sette C, Yang D, Eglen R, Wilhelm R, Shelton ER, Conti M (1995) Activationand selective Inhibitionof acyclic AMP- specificphosphodiesterase, PDE4D3. MolPharmacol 48:616-622
-
(1995)
MolPharmacol
, vol.48
, pp. 616-622
-
-
Alvarez, R.1
Sette, C.2
Yang, D.3
Eglen, R.4
Wilhelm, R.5
Shelton, E.R.6
Conti, M.7
-
3
-
-
0030712081
-
The GAF domain: An evolutionary link between diverse phototransducing proteins
-
DOI 10.1016/S0968-0004(97)01148-1, PII S0968000497011481
-
Aravind L, Ponting CP (1997) The GAF domain: an evolutionary link between diverse phototransducing proteins. Trends Biochem Sci 22:458-459 (Pubitemid 27515909)
-
(1997)
Trends in Biochemical Sciences
, vol.22
, Issue.12
, pp. 458-459
-
-
Aravind, L.1
Ponting, C.P.2
-
4
-
-
0037008722
-
2+- triggered membrane association with selectivity for interaction with phosphatidic acid
-
DOI 10.1074/jbc.M108353200
-
Baillie GS, Huston E, Scotland G, Hodgkin M, Gall I, Peden AH, MacKenzie C, Houslay ES, Currie R, Pettitt R, Walmsley AR, Wakelam MJO, Warwicker J, Houslay MD (2002) TAPAS-1, a novel microdomain within the unique N-terminal region of the PDE4A1 cAMP specific phosphodiesterase that allows rapid, Ca2+-triggered membrane association with selectivity for interaction with phosphatidic acid. J Biol Chem 277:28298-28309 (Pubitemid 34966785)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.31
, pp. 28298-28309
-
-
Baillie, G.S.1
Huston, E.2
Scotland, G.3
Hodgkin, M.4
Gall, I.5
Peden, A.H.6
MacKenzie, C.7
Houslay, E.S.8
Currie, R.9
Pettitt, T.R.10
Walmsley, A.R.11
Wakelam, M.J.O.12
Warwicker, J.13
Houslay, M.D.14
-
5
-
-
0037417890
-
i
-
DOI 10.1073/pnas.262787199
-
Baillie GS, Sood A, McPhee I, Gall I, Perry SJ, Lefkowitz RJ, Houslay MD (2003) b-arrestin mediated PDE4 cAMP phosphodiesterase recruitment regulates b2-adrenoceptor switching from Gs to Gi. Proc Natl Acad Sci 100:940-945 (Pubitemid 36183934)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.3
, pp. 940-945
-
-
Baillie, G.S.1
Sood, A.2
McPhee, I.3
Gall, I.4
Perry, S.J.5
Lefkowitz, R.J.6
Houslay, M.D.7
-
6
-
-
33748540402
-
Theophylline for COPD
-
DOI 10.1136/thx.2006.061002
-
Barnes P (2006) Theophylline for COPD. Thorax 61:742-744 (Pubitemid 44369394)
-
(2006)
Thorax
, vol.61
, Issue.9
, pp. 742-744
-
-
Barnes, P.J.1
-
7
-
-
14844303317
-
Phosphodiesterase 4D forms a cAMP diffusion barrier at the apical membrane of the airway epithelium
-
DOI 10.1074/jbc.M407521200
-
Barnes AP, Livera G, Huang P, Sun C, ONeal WK, Conti M, Stutts MJ, Milgram SL (2005) Phosphodiesterase 4D forms a cAMP diffusion barrier at the apical membrane of the airway epithelium. J Biol Chem 280:7997-8003 (Pubitemid 40349697)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.9
, pp. 7997-8003
-
-
Barnes, A.P.1
Livera, G.2
Huang, P.3
Sun, C.4
O'Neal, W.K.5
Conti, M.6
Stutts, M.J.7
Milgram, S.L.8
-
8
-
-
70450222522
-
Structural basis of phosphodiesterase 6 inhibition by the C-terminal region of the gamma-subunit
-
Barren B, Gakhar L, Muradov H, Boyd KK, Ramaswamy S, Artemyev NO (2009) Structural basis of phosphodiesterase 6 inhibition by the C-terminal region of the gamma-subunit. EMBO J 28:3613-3622
-
(2009)
EMBO J
, vol.28
, pp. 3613-3622
-
-
Barren, B.1
Gakhar, L.2
Muradov, H.3
Boyd, K.K.4
Ramaswamy, S.5
Artemyev, N.O.6
-
9
-
-
77949906745
-
CGMPphosphodiesterase 6, transducin and Wnt5a/Frizzled-2-signaling control cGMP and Ca (2+) homeostasis in melanoma cells
-
Bazhin AV, Tambor V, Dikov B, Philippov PP, Schadendorf D, Eichmuller SB (2010) cGMPphosphodiesterase 6, transducin and Wnt5a/Frizzled-2-signaling control cGMP and Ca(2+) homeostasis in melanoma cells. Cell Mol Life Sci 67:817-828
-
(2010)
Cell Mol Life Sci
, vol.67
, pp. 817-828
-
-
Bazhin, A.V.1
Tambor, V.2
Dikov, B.3
Philippov, P.P.4
Schadendorf, D.5
Eichmuller, S.B.6
-
10
-
-
0036729478
-
Cyclic nucleotide research - Still expanding after half a century
-
DOI 10.1038/nrm911
-
Beavo JA, Brunton LL (2002) Cyclic nucleotide research -still expanding after half a century. Nat Rev Mol Cell Biol 3:710-718 (Pubitemid 34987792)
-
(2002)
Nature Reviews Molecular Cell Biology
, vol.3
, Issue.9
, pp. 710-718
-
-
Beavo, J.A.1
Brunton, L.L.2
-
11
-
-
0028941919
-
Characterization of cyclic nucleotide phosphodiesterases with cyclic GMP analogs: Topology of the catalytic domains
-
Beltman J, Becker DE, Butt E, Jensen GS, Rybalkin SD, Jastorff B, Beavo JA (1995) Characterization of cyclic nucleotide phosphodiesterases with cyclic GMP analogs: topology of the catalytic domains. Mol Pharmacol 47:330-339
-
(1995)
Mol Pharmacol
, vol.47
, pp. 330-339
-
-
Beltman, J.1
Becker, D.E.2
Butt, E.3
Jensen, G.S.4
Rybalkin, S.D.5
Jastorff, B.6
Beavo, J.A.7
-
12
-
-
33748686575
-
Cyclic nucleotide phosphodiesterases: Molecular regulation to clinical use
-
DOI 10.1124/pr.58.3.5
-
Bender AT, Beavo J (2006) Cyclic nucleotide phosphodiesterases: molecualr regulation to clinical use. Pharmacol Rev 58:488-520 (Pubitemid 44394910)
-
(2006)
Pharmacological Reviews
, vol.58
, Issue.3
, pp. 488-520
-
-
Bender, A.T.1
Beavo, J.A.2
-
13
-
-
41149091747
-
Phosphorylation increases affinity of the phosphodiesterase-5 catalytic site for tadalafil
-
DOI 10.1124/jpet.107.133405
-
Bessay E, Blount M, Zoraghi R, Beasley A, Grimes K, Francis S, Corbin JD (2008) Phosphorylation increases affinity of the phosphodiesterase-5 catalytic site for tadalafil. J Pharmacol Exp Ther 325:62-68 (Pubitemid 351439156)
-
(2008)
Journal of Pharmacology and Experimental Therapeutics
, vol.325
, Issue.1
, pp. 62-68
-
-
Bessay, E.P.1
Blount, M.A.2
Zoraghi, R.3
Beasley, A.4
Grimes, K.A.5
Francis, S.H.6
Corbin, J.D.7
-
14
-
-
3042574999
-
Binding of tritiated sildenafil, tadalafil, or vardenafil to the phosphodiesterase-5 catalytic site displays potency, specificity, heterogeneity, and cGMP stimulation
-
DOI 10.1124/mol.66.1.144
-
Blount MA, Beasley A, Zoraghi R, Sekhar KR, Bessay EP, Francis SH, Corbin JD (2004) Binding of tritiated sildenafil, tadalafil, or vardenafil to the phosphodiesterase-5 catalytic site displays potency, specificity, heterogeneity, and cGMP stimulation. Mol Pharmacol 66:144-152 (Pubitemid 38822097)
-
(2004)
Molecular Pharmacology
, vol.66
, Issue.1
, pp. 144-152
-
-
Blount, M.A.1
Beasley, A.2
Zoraghi, R.3
Sekhar, K.R.4
Bessay, E.P.5
Francis, S.H.6
Corbin, J.D.7
-
15
-
-
33751161472
-
A 46-amino acid segment in phosphodiesterase-5 GAF-B domain provides for high vardenafil potency over sildenafil and tadalafil and is involved in phosphodiesterase-5 dimerization
-
Blount MA, Zoraghi R, Ke H, Bessay EP, Corbin JD, Francis SH (2006) A 46-amino acid segment in phosphodiesterase-5 GAF-B domain provides for high vardenafil potency over sildenafil and tadalafil and is involved in phosphodiesterase-5 dimerization. Mol Pharmacol 70:1822-1831
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1822-1831
-
-
Blount, M.A.1
Zoraghi, R.2
Ke, H.3
Bessay, E.P.4
Corbin, J.D.5
Francis, S.H.6
-
16
-
-
35548957803
-
Conversion of phosphodiesterase-5 (PDE5) catalytic site to higher affinity by PDE5 inhibitors
-
DOI 10.1124/jpet.107.126540
-
Blount MA, Zoraghi R, Bessay EP, Beasley A, Francis SH, Corbin JD (2007) Conversion of phosphodiesterase-5 (PDE5) catalytic site to higher affinity by PDE5 inhibitors. J Pharmacol Exp Ther 323:730-737 (Pubitemid 350005117)
-
(2007)
Journal of Pharmacology and Experimental Therapeutics
, vol.323
, Issue.2
, pp. 730-737
-
-
Blount, M.A.1
Zoraghi, R.2
Bessay, E.P.3
Beasley, A.4
Francis, S.H.5
Corbin, J.D.6
-
17
-
-
0027454556
-
A family of human phosphodiesterases homologous to the dunce learning and memory gene product of Drosophila melanogaster are potential targets for antidepressant drugs
-
Bolger G, Michaeli T, Martins T, St John T, Steiner B, Rodgers L, Riggs M, Wigler M, Ferguson K (1993) A family of human phosphodiesterases homologous to the dunce learning and memory gene product of Drosophila melanogaster are potential targets for antidepressant drugs. Mol Cell Biol 13:6558-6571 (Pubitemid 23292650)
-
(1993)
Molecular and Cellular Biology
, vol.13
, Issue.10
, pp. 6558-6571
-
-
Bolger, G.1
Michaeli, T.2
Martins, T.3
St. John, T.4
Steiner, B.5
Rodgers, L.6
Riggs, M.7
Wigler, M.8
Ferguson, K.9
-
18
-
-
0041856176
-
Attenuation of the activity of the cAMP-specific phosphodiesterase PDE4A5 by interaction with the immunophilin XAP2
-
DOI 10.1074/jbc.M303269200
-
Bolger GB, Peden AH, Steele MR, MacKenzie C, McEwan DG, Wallace DA, Huston E, Baillie GS, Houslay MD (2003) Attenuation of the activity of the cAMP-specific phosphodiesterase PDE4A5 by interaction with the immunophilin XAP2. J Biol Chem 278:33351-33363 (Pubitemid 37055787)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.35
, pp. 33351-33363
-
-
Bolger, G.B.1
Peden, A.H.2
Steele, M.R.3
MacKenzie, C.4
McEwan, D.G.5
Wallace, D.A.6
Huston, E.7
Baillie, G.S.8
Houslay, M.D.9
-
19
-
-
70350096419
-
Cellular functions of phosphodiesterase-4 enzymes
-
Beavo J, Francis S, Houslay MD (eds) CRC, Boca Raton, Ch. 6
-
Bolger GB, Conti M, Houslay MD (2006) Cellular functions of phosphodiesterase-4 enzymes. In: Beavo J, Francis S, Houslay MD (eds) Phosphodiesterases in health and disease. CRC, Boca Raton, pp 99-130, Ch. 6
-
(2006)
Phosphodiesterases in Health and Disease
, pp. 99-130
-
-
Bolger, G.B.1
Conti, M.2
Houslay, M.D.3
-
20
-
-
33751241720
-
Epac proteins: Multi-purpose cAMP targets
-
DOI 10.1016/j.tibs.2006.10.002, PII S0968000406002921
-
Bos JL (2006) Epac proteins: multi-purpose cAMP targets. Trends Biochem Sci 31:680-686 (Pubitemid 44791945)
-
(2006)
Trends in Biochemical Sciences
, vol.31
, Issue.12
, pp. 680-686
-
-
Bos, J.L.1
-
21
-
-
0022459260
-
Hydrolysis of cyclic nucleotides by a purified cGMP-stimulated phosphodiesterase: Structural requirements for hydrolysis
-
DOI 10.1016/0167-4838(86)90174-3
-
Braumann T, Erneux C, Petridis G, Stohrer WD, Jastorff B (1986) Hydrolysis of cyclic nucleotides by a purified cGMP-stimulated phosphodiesterase: structural requirements for hydrolysis. Biochim Biophys Acta 871:199-206 (Pubitemid 16085079)
-
(1986)
Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
, vol.871
, Issue.2
, pp. 199-206
-
-
Braumann, T.1
Erneux, C.2
Petridis, G.3
-
22
-
-
0018782888
-
Stereochemistry of internucleotide bond formation by polynucleotide phosphorylase from Micrococcus luteus
-
Burgers PM, Eckstein F (1979) Stereochemistry of internucleotide bond formation by polynucleotide phosphorylase from Micrococcus luteus. Biochemistry 18:450-454
-
(1979)
Biochemistry
, vol.18
, pp. 450-454
-
-
Burgers, P.M.1
Eckstein, F.2
-
23
-
-
74049158987
-
Design of phosphodiesterase 4D (PDE4D) allosteric modulators for enhancing cognition with improved safety
-
Burgin AB, Magnusson OT, Singh J, Witte P, Staker BL, Bjornsson JM, Thorsteinsdottir M, Hrafnsdottir S, Hagen T, Kiselyov AS, Stewart LJ, Gurney ME (2010) Design of phosphodiesterase 4D (PDE4D) allosteric modulators for enhancing cognition with improved safety. Nat Biotechnol 28:63-70
-
(2010)
Nat Biotechnol
, vol.28
, pp. 63-70
-
-
Burgin, A.B.1
Magnusson, O.T.2
Singh, J.3
Witte, P.4
Staker, B.L.5
Bjornsson, J.M.6
Thorsteinsdottir, M.7
Hrafnsdottir, S.8
Hagen, T.9
Kiselyov, A.S.10
Stewart, L.J.11
Gurney, M.E.12
-
24
-
-
33847612208
-
Adenosine 30, 50-phosphate in biological materials. I. Purification and properties of cyclic 30, 50-nucleotide phosphodiesterase and use of this enzyme to characterize adenosine 30, 50-phosphate in human urine
-
Butcher RW, Sutherland EW (1962) Adenosine 30, 50-phosphate in biological materials. I. Purification and properties of cyclic 30, 50-nucleotide phosphodiesterase and use of this enzyme to characterize adenosine 30, 50-phosphate in human urine. J Biol Chem 237:1244-1250
-
(1962)
J Biol Chem
, vol.237
, pp. 1244-1250
-
-
Butcher, R.W.1
Sutherland, E.W.2
-
25
-
-
0028923797
-
Characterization of cyclic nucleotide phosphodiesterases with cyclic AMP analogs: Topology of the catalytic sites and comparison with other cyclic AMP-binding proteins
-
Butt E, Beltman J, Becker DE, Jensen GS, Rybalkin SD, Jastorff B, Beavo JA (1995) Characterization of cyclic nucleotide phosphodiesterases with cyclic AMP analogs: topology of the catalytic sites and comparison with other cyclic AMP-binding proteins. Mol Pharmacol 47:340-347
-
(1995)
Mol Pharmacol
, vol.47
, pp. 340-347
-
-
Butt, E.1
Beltman, J.2
Becker, D.E.3
Jensen, G.S.4
Rybalkin, S.D.5
Jastorff, B.6
Beavo, J.A.7
-
26
-
-
33646795266
-
Cyclic guanosine monophosphate compartmentation in rat cardiac myocytes
-
Castro LR, Verde I, Cooper DM, Fischmeister R (2006) Cyclic guanosine monophosphate compartmentation in rat cardiac myocytes. Circulation 113:2221-2228
-
(2006)
Circulation
, vol.113
, pp. 2221-2228
-
-
Castro, L.R.1
Verde, I.2
Cooper, D.M.3
Fischmeister, R.4
-
27
-
-
0001834697
-
Structure-function relationships among cyclic nucleotide phosphodiesterases
-
Beavo J, Houslay MD (eds) Wiley, New York
-
Charbonneau H (1990) Structure-function relationships among cyclic nucleotide phosphodiesterases. In: Beavo J, Houslay MD (eds) Cyclic nucleotide phosphodiesterases: structure, regulation and drug action. Wiley, New York, pp 267-296
-
(1990)
Cyclic Nucleotide Phosphodiesterases: Structure, Regulation and Drug Action
, pp. 267-296
-
-
Charbonneau, H.1
-
28
-
-
41949117255
-
An insight into the pharmacophores of phosphodiesterase-5 inhibitors from synthetic and crystal structural studies
-
Chen G, Wang H, Robinson H, Cai J, Wan Y, Ke H (2008) An insight into the pharmacophores of phosphodiesterase-5 inhibitors from synthetic and crystal structural studies. Biochem Pharmacol 75:1717-1728
-
(2008)
Biochem Pharmacol
, vol.75
, pp. 1717-1728
-
-
Chen, G.1
Wang, H.2
Robinson, H.3
Cai, J.4
Wan, Y.5
Ke, H.6
-
29
-
-
0032406883
-
Partial characterization of the active site human platelet cAMP phosphodiesterase, PDE3A, by site-directed mutagenesis
-
DOI 10.1006/abbi.1998.0915
-
Cheung PP, Yu L, Zhang H, Colman RW (1998) Partial characterization of the active site human platelet cAMP phosphodiesterase, PDE3A, by site-directed mutagenesis. Arch Biochem Biophys 360:99-104 (Pubitemid 29010918)
-
(1998)
Archives of Biochemistry and Biophysics
, vol.360
, Issue.1
, pp. 99-104
-
-
Cheung, P.P.1
Yu, L.2
Zhang, H.3
Colman, R.W.4
-
30
-
-
55249096652
-
Ndel1 alters its conformation by sequestering cAMP-specific phosphodiesterase-4D3 (PDE4D3) in a manner that is dynamically regulated through Protein Kinase A (PKA)
-
Collins DM, Murdoch H, Dunlop AJ, Charych E, Baillie GS, Herberg FW, Brandon N, Prinz A, Houslay MD (2008) Ndel1 alters its conformation by sequestering cAMP-specific phosphodiesterase-4D3 (PDE4D3) in a manner that is dynamically regulated through Protein Kinase A (PKA). Cell Signal 20:2356-2369
-
(2008)
Cell Signal
, vol.20
, pp. 2356-2369
-
-
Collins, D.M.1
Murdoch, H.2
Dunlop, A.J.3
Charych, E.4
Baillie, G.S.5
Herberg, F.W.6
Brandon, N.7
Prinz, A.8
Houslay, M.D.9
-
31
-
-
34447265905
-
Biochemistry and physiology of cyclic nucleotide phosphodiesterases: Essential components in cyclic nucleotide signaling
-
Conti M, Beavo J (2007) Biochemistry and physiology of cyclic nucleotide phosphodiesterases: essential components in cyclic nucleotide signaling. Annu Rev Biochem 76:481-511
-
(2007)
Annu Rev Biochem
, vol.76
, pp. 481-511
-
-
Conti, M.1
Beavo, J.2
-
32
-
-
0037458648
-
Cyclic AMP-specific PDE4 phosphodiesterases as critical components of cyclic AMP signaling
-
DOI 10.1074/jbc.R200029200
-
Conti M, Richter W, Mehats C, Livera G, Park JY, Jin C (2003) Cyclic AMP-specific PDE4 phosphodiesterases as critical components of cyclic AMP signaling. J Biol Chem 278:5493-5496 (Pubitemid 36800786)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.8
, pp. 5493-5496
-
-
Conti, M.1
Richter, W.2
Mehats, C.3
Livera, G.4
Park, J.-Y.5
Jin, C.6
-
33
-
-
0033553509
-
Cyclic GMP phosphodiesterase-5: Target of sildenafil
-
Corbin JD, Francis SH (1999) Cyclic GMP phosphodiesterase-5: target of sildenafil. J Biol Chem 274:13729-13732
-
(1999)
J Biol Chem
, vol.274
, pp. 13729-13732
-
-
Corbin, J.D.1
Francis, S.H.2
-
34
-
-
0017684387
-
Compartmentalization of adenosine 3':5' monophosphate and adenosine 3':5' monophosphate dependent protein kinase in heart tissue
-
Corbin JD, Sugden PH, Lincoln TM, Keely SL (1977) Compartmentalization of adenosine 30:50-monophosphate and adenosine 30:50-monophosphate-dependent protein kinase in heart tissue. J Biol Chem 252:3854-3861 (Pubitemid 8127237)
-
(1977)
Journal of Biological Chemistry
, vol.252
, Issue.11
, pp. 3854-3861
-
-
Corbin, J.D.1
Sugden, P.H.2
Lincoln, T.M.3
Keely, S.L.4
-
35
-
-
0034108626
-
Phosphorylation of phosphodiesterase-5 by cyclic nucleotide-dependent protein kinase alters its catalytic and allosteric cGMP-binding activities
-
DOI 10.1046/j.1432-1327.2000.01297.x
-
Corbin JD, Turko IV, Beasley A, Francis SH (2000) Phosphorylation of phosphodiesterase-5 by cyclic nucleotide-dependent protein kinase alters its catalytic and allosteric cGMP-binding activities. Eur J Biochem 267:2760-2767 (Pubitemid 30304274)
-
(2000)
European Journal of Biochemistry
, vol.267
, Issue.9
, pp. 2760-2767
-
-
Corbin, J.D.1
Turko, I.V.2
Beasley, A.3
Francis, S.H.4
-
36
-
-
0038024614
-
3H]sildenafil binding to phosphodiesterase-5 is specific, kinetically heterogeneous, and stimulated by cGMP
-
DOI 10.1124/mol.63.6.1364
-
Corbin JD, Blount MA, Weeks JL 2nd, Beasley A, Kuhn KP, Ho YS, Saidi LF, Hurley JH, Kotera J, Francis SH (2003) [3H]sildenafil binding to phosphodiesterase-5 is specific, kinetically heterogeneous, and stimulated by cGMP. Mol Pharmacol 63:1364-1372 (Pubitemid 36627232)
-
(2003)
Molecular Pharmacology
, vol.63
, Issue.6
, pp. 1364-1372
-
-
Corbin, J.D.1
Blount, M.A.2
Weeks II, J.L.3
Beasley, A.4
Kuhn, K.P.5
Ho, Y.S.J.6
Saidi, L.F.7
Hurley, J.H.8
Kotera, J.9
Francis, S.H.10
-
37
-
-
0027535918
-
Investigation into the role of phosphodiesterase IV in bronchorelaxation, including studies with human bronchus
-
Cortijo J, Bou J, Beleta J, Cardelus I, Llenas J, Morcillo E, Gristwood RW (1993) Investigation into the role of phosphodiesterase IV in bronchorelaxation, including studies with human bronchus. Br J Pharmacol 108:562-568 (Pubitemid 23032571)
-
(1993)
British Journal of Pharmacology
, vol.108
, Issue.2
, pp. 562-568
-
-
Cortijo, J.1
Bou, J.2
Beleta, J.3
Cardelus, I.4
Llenas, J.5
Morcillo, E.6
Gristwood, R.W.7
-
38
-
-
85132536724
-
Photoreceptor phosphodiesterase (PDE6): AG-protein-activated PDE regulatingvisual excitation in rod and cone photoreceptor cells
-
Beavo J, Francis SH, Houslay MD(eds) CRC Press, Boca Raton
-
Cote RH (2006) Photoreceptor phosphodiesterase (PDE6): aG-protein-activated PDE regulatingvisual excitation in rod and cone photoreceptor cells. In: Beavo J, Francis SH, Houslay MD(eds) Cyclic nucleotidephosphodiesterasesinhealthanddisease. CRC Press, Boca Raton, pp 165-193
-
(2006)
Cyclic Nucleotidephosphodiesterasesinhealthanddisease
, pp. 165-193
-
-
Cote, R.H.1
-
39
-
-
0002332460
-
Effects of theophylline and non-selective xanthine derivatives on PDE isoenzymes and cellular function
-
Schudt C, Dent G, Rabe KF (eds) Academic, San Diego
-
Dent G, Rabe K (1996) Effects of theophylline and non-selective xanthine derivatives on PDE isoenzymes and cellular function. In: Schudt C, Dent G, Rabe KF (eds) Handbook of immunopharmacology: phosphodiesterase inhibitors. Academic, San Diego, pp 41-64
-
(1996)
Handbook of Immunopharmacology: Phosphodiesterase Inhibitors
, pp. 41-64
-
-
Dent, G.1
Rabe, K.2
-
40
-
-
0019945542
-
Paradoxical stimulation by 1-methyl-3-isobutylxanthine of rat liver cyclic AMP phosphodiesterase activity
-
DOI 10.1016/0014-5793(82)80146-4
-
Erneux C, Miot F, Boeynaems JM, Dumont JE (1982) Paradoxical stimulation by 1-methyl-3-isobutylxanthine of rat liver cyclic AMP phosphodiesterase activity. FEBS Lett 142:251-254 (Pubitemid 12050506)
-
(1982)
FEBS Letters
, vol.142
, Issue.2
, pp. 251-254
-
-
Erneux, C.1
Miot, F.2
Boeynaems, J.M.3
Dumont, J.E.4
-
41
-
-
0033521110
-
Expression of an active, monomeric catalytic domain of the cGMP-binding cGMP-specific phosphodiesterase (PDE5)
-
Fink TL, Francis SH, Beasley A, Grimes KA, Corbin JD (1999) Expression of an active, monomeric catalytic domain of the cGMP-binding cGMP-specific phosphodiesterase (PDE5). J Biol Chem 274:34613-34620 (Pubitemid 129509498)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.49
, pp. 34613-34620
-
-
Fink, T.L.1
Francis, S.H.2
Beasley, A.3
Grimes, K.A.4
Corbin, J.D.5
-
42
-
-
0032848914
-
Cyclic nucleotide-dependent protein kinases: Intracellular receptors for cAMP and cGMP action
-
DOI 10.1080/10408369991239213
-
Francis SH, Corbin JD (1999) Cyclic nucleotide-dependent protein kinases: intracellular receptors for cAMP and cGMP action. Crit Rev Clin Lab Sci 36:275-328 (Pubitemid 29431414)
-
(1999)
Critical Reviews in Clinical Laboratory Sciences
, vol.36
, Issue.4
, pp. 275-328
-
-
Francis, S.H.1
Corbin, J.D.2
-
43
-
-
27744494899
-
Phosphodiesterase-5 inhibition: The molecular biology of erectile function and dysfunction
-
DOI 10.1016/j.ucl.2005.08.001, PII S0094014305000807, Erectile Dysfunction
-
Francis SH, Corbin JD (2005) Phosphodiesterase-5 inhibition: the molecular biology of erectile function and dysfunction. Urol Clin North Am 32:419-429 (Pubitemid 41607530)
-
(2005)
Urologic Clinics of North America
, vol.32
, Issue.4
, pp. 419-429
-
-
Francis, S.H.1
Corbin, J.D.2
-
44
-
-
79960920515
-
Phosphodiesterase-5
-
Bradshaw RA, Dennis EA (eds) 2nd edn. Academic, Oxford
-
Francis SH, Corbin JD (2009) Phosphodiesterase-5. In: Bradshaw RA, Dennis EA (eds) Handbook of cell signaling, vol 2, 2nd edn. Academic, Oxford, pp 1439-1444
-
(2009)
Handbook of Cell Signaling
, vol.2
, pp. 1439-1444
-
-
Francis, S.H.1
Corbin, J.D.2
-
45
-
-
0028070403
-
Zinc interactions and conserved motifs of the cGMP-binding cGMP-specific phosphodiesterase suggest that it is a zinc hydrolase
-
Francis SH, Colbran JL, McAllister-Lucas LM, Corbin JD (1994) Zinc interactions and conserved motifs of the cGMP-binding cGMP-specific phosphodiesterase suggest that it is a zinc hydrolase. J Biol Chem 269:22477-22480 (Pubitemid 24273347)
-
(1994)
Journal of Biological Chemistry
, vol.269
, Issue.36
, pp. 22477-22480
-
-
Francis, S.H.1
Colbran, J.L.2
McAllister-Lucas, L.M.3
Corbin, J.D.4
-
46
-
-
85132510350
-
Phosphodiesterase-5: Molecular characteristics relating to structure, function, and regulation
-
Beavo SHF JA, Houslay MD (eds) CRC Press, Boca Raton
-
Francis SH, Zoraghi R, Kotera J, Ke H, Bessay EP, Blount MA, Corbin JD (2006) Phosphodiesterase-5: molecular characteristics relating to structure, function, and regulation. In: Beavo SHF JA, Houslay MD (eds) Cyclic nucleotide phosphodiesterases in health and disease. CRC Press, Boca Raton, pp 131-164
-
(2006)
Cyclic Nucleotide Phosphodiesterases in Health and Disease
, pp. 131-164
-
-
Francis, S.H.1
Zoraghi, R.2
Kotera, J.3
Ke, H.4
Bessay, E.P.5
Blount, M.A.6
Corbin, J.D.7
-
47
-
-
48249105061
-
Molecular mechanisms that could contribute to prolonged effectiveness of PDE5 inhibitors to improve erectile function
-
Francis SH, Morris GZ, Corbin JD (2008) Molecular mechanisms that could contribute to prolonged effectiveness of PDE5 inhibitors to improve erectile function. Int J Impot Res 20: 333-342
-
(2008)
Int J Impot Res
, vol.20
, pp. 333-342
-
-
Francis, S.H.1
Morris, G.Z.2
Corbin, J.D.3
-
48
-
-
0032407722
-
YC-1 potentiates nitric oxide- and carbon monoxide-induced cyclic GMP effects in human platelets
-
Friebe A, Mullershausen F, Smolenski A, Walter U, Schultz G, Koesling D (1998) YC-1 potentiates nitric oxide-and carbon monoxide-induced cyclic GMP effects in human platelets. Mol Pharmacol 54:962-967 (Pubitemid 29002038)
-
(1998)
Molecular Pharmacology
, vol.54
, Issue.6
, pp. 962-967
-
-
Friebe, A.1
Mullershausen, F.2
Smolenski, A.3
Walter, U.4
Schultz, G.5
Koesling, D.6
-
49
-
-
0346643472
-
Effects of the soluble guanylyl cyclase activator, YC-1, on vascular tone, cyclic GMP levels and phosphodiesterase activity
-
DOI 10.1038/sj.bjp.0702495
-
Galle J, Zabel U, Hubner U, Hatzelmann A, Wagner B, Wanner C, Schmidt HH (1999) Effects of the soluble guanylyl cyclase activator, YC-1, on vascular tone, cyclic GMP levels and phosphodiesterase activity. Br J Pharmacol 127:195-203 (Pubitemid 29213249)
-
(1999)
British Journal of Pharmacology
, vol.127
, Issue.1
, pp. 195-203
-
-
Galle, J.1
Zabel, U.2
Hubner, U.3
Hatzelmann, A.4
Wagner, B.5
Wanner, C.6
Schmidt, H.H.H.W.7
-
50
-
-
52949124088
-
Reinventing the wheel: Nonselective phosphodiesterase inhibitors for chronic inflammatory diseases
-
Beavo JA, Francis SH, Houslay MD (eds) CRC Press, Boca Raton
-
Giembycz MA (2006) Reinventing the wheel: nonselective phosphodiesterase inhibitors for chronic inflammatory diseases. In: Beavo JA, Francis SH, Houslay MD (eds) Cyclic nucleotide phosphodiesterases in health and disease. CRC Press, Boca Raton, pp 649-665
-
(2006)
Cyclic Nucleotide Phosphodiesterases in Health and Disease
, pp. 649-665
-
-
Giembycz, M.A.1
-
51
-
-
0034838812
-
Allosteric sites of phosphodiesterase-5 (PDE5). A potential role in negative feedback regulation of cGMP signaling in corpus cavernosum
-
DOI 10.1046/j.1432-1327.2001.02233.x
-
Gopal VK, Francis SH, Corbin JD (2001) Allosteric sites of phosphodiesterase-5 (PDE5). A potential role in negative feedback regulation of cGMP signaling in corpus cavernosum. Eur J Biochem 268:3304-3312 (Pubitemid 32823005)
-
(2001)
European Journal of Biochemistry
, vol.268
, Issue.11
, pp. 3304-3312
-
-
Gopal, V.K.1
Francis, S.H.2
Corbin, J.D.3
-
52
-
-
14844364419
-
2+-calmodulin-dependent phosphodiesterase (PDE1): Current perspectives
-
DOI 10.1016/j.cellsig.2004.12.017
-
Goraya TA, Cooper DM (2005) Ca2+-calmodulin-dependent phosphodiesterase (PDE1): current perspectives. Cell Signal 17:789-797 (Pubitemid 40353649)
-
(2005)
Cellular Signalling
, vol.17
, Issue.7
, pp. 789-797
-
-
Goraya, T.A.1
Cooper, D.M.F.2
-
53
-
-
33646379135
-
CAMP is a ligand for the tandem GAF domain of human phosphodiesterase 10 and cGMP for the tandem GAF domain of phosphodiesterase 11
-
DOI 10.1074/jbc.M511468200
-
Gross-Langenhoff M, Hofbauer K, Weber J, Schultz A, Schultz JE (2006) cAMP is a ligand for the tandem GAF domain of human phosphodiesterase 10 and cGMP for the tandem GAF domain of phosphodiesterase 11. J Biol Chem 281:2841-2846 (Pubitemid 43845749)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.5
, pp. 2841-2846
-
-
Gross-Langenhoff, M.1
Hofbauer, K.2
Weber, J.3
Schultz, A.4
Schultz, J.E.5
-
54
-
-
79960902354
-
Small molecule allosteric modulators of phosphodiesterase 4
-
Francis SH, Conti M, Houslay MD (eds) Springer, Heidelberg
-
Gurney ME, Burgin AB, Magnusson OT, Stewart LJ (2011) Small molecule allosteric modulators of phosphodiesterase 4. Francis SH, Conti M, Houslay MD (eds) Phosphodiesterases as drug targets. Springer, Heidelberg
-
(2011)
Phosphodiesterases As Drug Targets
-
-
Gurney, M.E.1
Burgin, A.B.2
Magnusson, O.T.3
Stewart, L.J.4
-
55
-
-
33744959735
-
PDE7A1, a cAMP-specific phosphodiesterase, inhibits cAMP-dependent protein kinase by a direct interaction with C
-
DOI 10.1074/jbc.M601333200
-
Han P, Sonati P, Rubin C, Michaeli T (2006) PDE7A1, a cAMP-specific phosphodiesterase, inhibits cAMP-dependent protein kinase by a direct interaction with C. J Biol Chem 281:15050-15057 (Pubitemid 43855093)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.22
, pp. 15050-15057
-
-
Han, P.1
Sonati, P.2
Rubin, C.3
Michaeli, T.4
-
56
-
-
50349084137
-
Crystal structure of theGAF-B domain from human phosphodiesterase 10A complexed with its ligand, cAMP
-
Handa N, Mizohata E, Kishishita S, Toyama M, Morita S, Uchikubo-Kamo T, Akasaka R, Omori K, Kotera J, Terada T, Shirouzu M, Yokoyama S (2008) Crystal structure of theGAF-B domain from human phosphodiesterase 10A complexed with its ligand, cAMP. J Biol Chem 283:19657-19664
-
(2008)
J Biol Chem
, vol.283
, pp. 19657-19664
-
-
Handa, N.1
Mizohata, E.2
Kishishita, S.3
Toyama, M.4
Morita, S.5
Uchikubo-Kamo, T.6
Akasaka, R.7
Omori, K.8
Kotera, J.9
Terada, T.10
Shirouzu, M.11
Yokoyama, S.12
-
57
-
-
0018356415
-
Hormonally specific expression of cardiac protein kinase activity
-
DOI 10.1073/pnas.76.4.1570
-
Hayes JS, Brunton LL, Brown JH, Reese JB, Mayer SE (1979) Hormonally specific expression of cardiac protein kinase activity. Proc Natl Acad Sci USA 76:1570-1574 (Pubitemid 9175360)
-
(1979)
Proceedings of the National Academy of Sciences of the United States of America
, vol.76
, Issue.4
, pp. 1570-1574
-
-
Hayes, J.S.1
Brunton, L.L.2
Brown, J.H.3
-
58
-
-
0034617193
-
Multiple zinc binding sites in retinal rod cGMP phosphodiesterase, PDE6αβ
-
DOI 10.1074/jbc.M000440200
-
He F, Seryshev AB, Cowan CW, Wensel TG (2000) Multiple zinc binding sites in retinal rod cGMP phosphodiesterase, PDE6alpha beta. J Biol Chem 275:20572-20577 (Pubitemid 30457641)
-
(2000)
Journal of Biological Chemistry
, vol.275
, Issue.27
, pp. 20572-20577
-
-
He, F.1
Seryshev, A.B.2
Cowan, C.W.3
Wensel, T.G.4
-
59
-
-
53049094120
-
Solution structure of the cGMP binding GAF domain from phosphodiesterase 5: Insights into nucleotide specificity, dimerization, and cGMP-dependent conformational change
-
Heikaus CC, Stout JR, Sekharan MR, Eakin CM, Rajagopal P, Brzovic PS, Beavo JA, Klevit RE (2008) Solution structure of the cGMP binding GAF domain from phosphodiesterase 5: insights into nucleotide specificity, dimerization, and cGMP-dependent conformational change. J Biol Chem 283:22749-22759
-
(2008)
J Biol Chem
, vol.283
, pp. 22749-22759
-
-
Heikaus, C.C.1
Stout, J.R.2
Sekharan, M.R.3
Eakin, C.M.4
Rajagopal, P.5
Brzovic, P.S.6
Beavo, J.A.7
Klevit, R.E.8
-
60
-
-
33748558750
-
Inhibition of reactive nitrogen species production in COPD airways: Comparison of inhaled corticosteroid and oral theophylline
-
DOI 10.1136/thx.200X.058156
-
Hirano T, Yamagata T, Gohda M, Yamagata Y, Ichikawa T, Yanagisawa S, Ueshima K, Akamatsu K, Nakanishi M, Matsunaga K, Minakata Y, Ichinose M (2006) Inhibition of reactive nitrogen specids production in COPD airways: comparison between inhaled corticosteroid and oral theophylline. Thorax 61:761-766 (Pubitemid 44369399)
-
(2006)
Thorax
, vol.61
, Issue.9
, pp. 761-766
-
-
Hirano, T.1
Yamagata, T.2
Gohda, M.3
Yamagata, Y.4
Ichikawa, T.5
Yanagisawa, S.6
Ueshima, K.7
Akamatsu, K.8
Nakanishi, M.9
Matsunaga, K.10
Minakata, Y.11
Ichinose, M.12
-
61
-
-
0032127768
-
CAMP-specific phosphodiesterase HSPDE4D3 mutants which mimic activation and changes in rolipram inhibition triggered by protein kinase A phosphorylation of Ser-54: Generation of a molecular model
-
Hoffmann R, Wilkinson IR, McCallum JF, Engels P, Houslay MD (1998) cAMP-specific phosphodiesterase HSPDE4D3 mutants which mimic activation and changes in rolipram inhibition triggered by protein kinase A phosphorylation of Ser-54: generation of a molecular model. Biochem J 333:139-149 (Pubitemid 28342503)
-
(1998)
Biochemical Journal
, vol.333
, Issue.1
, pp. 139-149
-
-
Hoffmann, R.1
Wilkinson, I.R.2
McCallum, J.F.3
Engels, P.4
Houslay, M.D.5
-
62
-
-
0035224418
-
Intracellular targeting and regulation of PDE4 cAMP specific Phosphodiesterases
-
Houslay MD (2001) Intracellular targeting and regulation of PDE4 cAMP specific Phosphodiesterases. Prog Nucleic Acid Res Mol Biol 69:249-315
-
(2001)
Prog Nucleic Acid Res Mol Biol
, vol.69
, pp. 249-315
-
-
Houslay, M.D.1
-
63
-
-
75749117558
-
Underpinning compartmentalised cAMP signalling through targeted cAMP breakdown
-
Houslay MD (2010) Underpinning compartmentalised cAMP signalling through targeted cAMP breakdown. Trends Biochem Sci 35:91-100
-
(2010)
Trends Biochem Sci
, vol.35
, pp. 91-100
-
-
Houslay, M.D.1
-
64
-
-
0037443097
-
PDE4 cAMP phosphodiesterases: Modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization
-
DOI 10.1042/BJ20021698
-
Houslay MD, Adams DR (2003) PDE4 cAMP phosphodiesterases: modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization. Biochem J 370:1-18 (Pubitemid 36259414)
-
(2003)
Biochemical Journal
, vol.370
, Issue.1
, pp. 1-18
-
-
Houslay, M.D.1
Adams, D.R.2
-
66
-
-
27344449614
-
Keynote review: Phosphodiesterase-4 as a therapeutic target
-
DOI 10.1016/S1359-6446(05)03622-6, PII S1359644605036226
-
Houslay MD, Schafer P, Zhang K (2005) Keynote review: phosphodiesterase-4 as a therapeutic target. Drug Discov Today 10:1503-1519 (Pubitemid 41527193)
-
(2005)
Drug Discovery Today
, vol.10
, Issue.22
, pp. 1503-1519
-
-
Houslay, M.D.1
Schafer, P.2
Zhang, K.Y.J.3
-
67
-
-
34247105883
-
CAMP-specific phosphodiesterase-4 enzymes in the cardiovascular system: A molecular toolbox for generating compartmentalized cAMP signaling
-
DOI 10.1161/01.RES.0000261934.56938.38, PII 0000301220070413000007
-
Houslay MD, Baillie GS, Maurice DH (2007) cAMP-specific phosphodiesterase-4 enzymes in the cardiovascular system: a molecular toolbox for generating compartmentalized cAMP signaling. Circ Res 100:950-966 (Pubitemid 46598920)
-
(2007)
Circulation Research
, vol.100
, Issue.7
, pp. 950-966
-
-
Houslay, M.D.1
Baillie, G.S.2
Maurice, D.H.3
-
68
-
-
0038154006
-
Three-dimensional structures of PDE4D in complex with roliprams and implication on inhibitor selectivity
-
DOI 10.1016/S0969-2126(03)00123-0
-
Huai Q, Wang H, Sun Y, Kim HY, Liu Y, Ke H (2003) Three-dimensional structures of PDE4D in complex with roliprams and implication on inhibitor selectivity. Structure 11:865-873 (Pubitemid 36833272)
-
(2003)
Structure
, vol.11
, Issue.7
, pp. 865-873
-
-
Huai, Q.1
Wang, H.2
Sun, Y.3
Kim, H.-Y.4
Liu, Y.5
Ke, H.6
-
69
-
-
3042795876
-
Crystal structure of phosphodiesterase 9 shows orientation variation of inhibitor 3-isobutyl-1-methylxanthine binding
-
DOI 10.1073/pnas.0401120101
-
Huai Q, Wang H, Zhang W, Colman RW, Robinson H, Ke H (2004) Crystal structure of phosphodiesterase 9 shows orientation variation of inhibitor 3-isobutyl-1-methylxanthine binding. Proc Natl Acad Sci USA 101(26):9624-9629 (Pubitemid 38869286)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.26
, pp. 9624-9629
-
-
Huai, Q.1
Wang, H.2
Zhang, W.3
Colman, R.W.4
Robinson, H.5
Ke, H.6
-
70
-
-
9144263723
-
Molecular determinants of cGMP binding to chicken cone photoreceptor phosphodiesterase
-
DOI 10.1074/jbc.M404338200
-
Huang D, Hinds TR, Martinez SE, Doneanu C, Beavo JA (2004) Molecular determinants of cGMP binding to chicken cone photoreceptor phosphodiesterase. J Biol Chem 279:48143-48151 (Pubitemid 39540969)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.46
, pp. 48143-48151
-
-
Huang, D.1
Hinds, T.R.2
Martinez, S.E.3
Doneanu, C.4
Beavo, J.A.5
-
71
-
-
0029857245
-
The human cyclic AMP-specific phosphodiesterase PDE-46 (HSPDE4A4B) expressed in transfected COS7 cells occurs as both particulate and cytosolic species that exhibit distinct kinetics of inhibition by the antidepressant rolipram
-
DOI 10.1074/jbc.271.49.31334
-
Huston E, Pooley L, Julien P, Scotland G, McPhee I, Sullivan M, Bolger G, Houslay MD (1996) The human cyclic AMP-specific phosphodiesterase PDE-46 (HSPDE4A4B) expressed in transfected COS7 cells occurs as both particulate and cytosolic species that exhibit distinct kinetics of inhibition by the antidepressant rolipram. J Biol Chem 271:31334-31344 (Pubitemid 26408583)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.49
, pp. 31334-31344
-
-
Huston, E.1
Pooley, L.2
Julien, P.3
Scotland, G.4
McPhee, I.5
Sullivan, M.6
Bolger, G.7
Houslay, M.D.8
-
72
-
-
33747167330
-
CAMP phosphodiesterase-4A1 (PDE4A1) has provided the paradigm for the intracellular targeting of phosphodiesterases, a process that underpins compartmentalized cAMP signalling
-
DOI 10.1042/BST0340504
-
Huston E, Houslay TM, Baillie GS, Houslay MD (2006) cAMP phosphodiesterase-4A1 (PDE4A1) has provided the paradigm for the intracellular targeting of phosphodiesterases, a process that underpins compartmentalized cAMP signalling. Biochem Soc Trans 34:504-509 (Pubitemid 44230748)
-
(2006)
Biochemical Society Transactions
, vol.34
, Issue.4
, pp. 504-509
-
-
Huston, E.1
Houslay, T.M.2
Baillie, G.S.3
Houslay, M.D.4
-
73
-
-
51349087322
-
EPAC and PKA allow cAMP dual control over DNA-PK nuclear translocation
-
Huston E, Lynch M, Mohamed A, Collins DM, Hill EV, MacLeod R, Krause E, Baillie GS, Houslay MD (2008) EPAC and PKA allow cAMP dual control over DNA-PK nuclear translocation. Proc Natl Acad Sci USA 105:12791-12796
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 12791-12796
-
-
Huston, E.1
Lynch, M.2
Mohamed, A.3
Collins, D.M.4
Hill, E.V.5
MacLeod, R.6
Krause, E.7
Baillie, G.S.8
Houslay, M.D.9
-
74
-
-
0029979738
-
Mapping the functional domains of human recombinant phosphodiesterase 4A: Structural requirements for catalytic activity and rolipram binding
-
Jacobitz S, McLaughlin MM, Livi GP, Burman M, Torphy TJ (1996) Mapping the functional domains of human recombinant phosphodiesterase 4A: structural requirements for catalytic activity and rolipram binding. Mol Pharmacol 50:891-899 (Pubitemid 26347710)
-
(1996)
Molecular Pharmacology
, vol.50
, Issue.4
, pp. 891-899
-
-
Jacobitz, S.1
Mclaughlin, M.M.2
Livi, G.P.3
Burman, M.4
Torphy, T.J.5
-
75
-
-
0020131864
-
A stereochemical investigation of the hydrolysis of cyclic AMP and the (Sp)-and (Rp)-diastereoisomers of adenosine cyclic 30:50-phosphorothioate by bovine heart and bakers-yeast cyclic AMP phosphodiesterases
-
Jarvest RL, Lowe G, Baraniak J, Stec WJ (1982) A stereochemical investigation of the hydrolysis of cyclic AMP and the (Sp)-and (Rp)-diastereoisomers of adenosine cyclic 30:50-phosphorothioate by bovine heart and bakers-yeast cyclic AMP phosphodiesterases. Biochem J 203:461-470
-
(1982)
Biochem J
, vol.203
, pp. 461-470
-
-
Jarvest, R.L.1
Lowe, G.2
Baraniak, J.3
Stec, W.J.4
-
76
-
-
77953103987
-
Vinpocetine inhibits NF-kappaB-dependent inflammation via an IKK-dependent but PDEindependent mechanism
-
Jeon KI, Xu X, Aizawa T, Lim JH, Jono H, Kwon DS, Abe J, Berk BC, Li JD, Yan C (2010) Vinpocetine inhibits NF-kappaB-dependent inflammation via an IKK-dependent but PDEindependent mechanism. Proc Natl Acad Sci USA 107:9795-9800
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 9795-9800
-
-
Jeon, K.I.1
Xu, X.2
Aizawa, T.3
Lim, J.H.4
Jono, H.5
Kwon, D.S.6
Abe, J.7
Berk, B.C.8
Li, J.D.9
Yan, C.10
-
77
-
-
0026753496
-
Characterization of the structure of a low Km, rolipram-sensitive cAMP phosphodiesterase. Mapping of the catalytic domain
-
Jin SL, Swinnen JV, Conti M (1992) Characterization of the structure of a lowKm, rolipram-sensitive cAMP phosphodiesterase. Mapping of the catalytic domain. J Biol Chem 267:18929-18939
-
(1992)
J Biol Chem
, vol.267
, pp. 18929-18939
-
-
Jin, S.L.1
Swinnen, J.V.2
Conti, M.3
-
78
-
-
0032692936
-
Impaired growth and fertility of cAMP-specific phosphodiesterase PDE4D- deficient mice
-
DOI 10.1073/pnas.96.21.11998
-
Jin SC, Richard FJ, Kuo WP, DErcole AJ, Conti M (1999) Impaired growth and fertility of cAMP-specific phosphodiesterase PDE4D-deficient mice. Proc Natl Acad Sci USA 96: 11998-12003 (Pubitemid 29502847)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.21
, pp. 11998-12003
-
-
Jin, S.L.C.1
Richard, F.J.2
Kuo, W.-P.3
D'Ercole, A.J.4
Conti, M.5
-
79
-
-
0030940907
-
A subset of olfactory neurons that selectively express cGMP-stimulated phosphodiesterase (PDE2) and guanylyl cyclase-D define a unique olfactory signal transduction pathway
-
DOI 10.1073/pnas.94.7.3388
-
Juilfs DM, FÜlle HJ, Zhao AZ, Houslay MD, Garbers DL, Beavo JA (1997) A subset of olfactory neurons that selectively express cGMP-stimulated phosphodiesterase (PDE2) and guanylyl cyclase-D define a unique olfactory signal transduction pathway. Proc Natl Acad Sci USA 94:3388-3395 (Pubitemid 27157322)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.7
, pp. 3388-3395
-
-
Juilfs, D.M.1
Fulle, H.-J.2
Zhao, A.Z.3
Houslay, M.D.4
Garbers, D.L.5
Beavo, J.A.6
-
80
-
-
8444227836
-
Disposition of CP-671, 305, a selective phosphodiesterase 4 inhibitor in preclinical species
-
DOI 10.1080/00498250400005682
-
Kalgutkar AS, Choo E, Taylor TJ, Marfat A (2004) Disposition of CP-671, 305, a selective phosphodiesterase 4 inhibitor in preclinical species. Xenobiotica 34:755-770 (Pubitemid 39487050)
-
(2004)
Xenobiotica
, vol.34
, Issue.8
, pp. 755-770
-
-
Kalgutkar, A.S.1
Choo, E.2
Taylor, T.J.3
Marfat, A.4
-
81
-
-
0141885183
-
Cilostazol as a unique antithrombotic agent
-
DOI 10.2174/1381612033453910
-
Kambayashi J, Liu Y, Sun B, Shakur Y, Yoshitake M, Czerwiec F (2003) Cilostazol as a unique antithrombotic agent. Curr Pharm Des 9:2289-2302 (Pubitemid 37236353)
-
(2003)
Current Pharmaceutical Design
, vol.9
, Issue.28
, pp. 2289-2302
-
-
Kambayashi, J.1
Liu, Y.2
Sun, B.3
Shakur, Y.4
Yoshitake, M.5
Czerwiec, F.6
-
82
-
-
85132521865
-
Bench to bedside: Multiple actions of the PDE3 inhibitor cilostazol
-
Beavo JA, Francis SH, Houslay MD (eds) CRC Press, Boca Raton
-
Kambayashi J, Shakur Y, Liu Y (2006) Bench to bedside: multiple actions of the PDE3 inhibitor cilostazol. In: Beavo JA, Francis SH, Houslay MD (eds) Cyclic nucleotide phosphodiesterases in health and disease. CRC Press, Boca Raton, pp 627-648
-
(2006)
Cyclic Nucleotide Phosphodiesterases in Health and Disease
, pp. 627-648
-
-
Kambayashi, J.1
Shakur, Y.2
Liu, Y.3
-
83
-
-
0347519217
-
DA-8159, a new PDE5 inhibitor, attenuates the development of compensatory right ventricular hypertrophy in a rat model of pulmonary hypertension
-
Kang KK, Ahn GJ, Sohn YS, Ahn BO, Kim WB (2003) DA-8159, a new PDE5 inhibitor, attenuates the development of compensatory right ventricular hypertrophy in a rat model of pulmonary hypertension. J Int Med Res 31:517-528 (Pubitemid 38008687)
-
(2003)
Journal of International Medical Research
, vol.31
, Issue.6
, pp. 517-528
-
-
Kang, K.K.1
Ahn, G.J.2
Sohn, Y.S.3
Ahn, B.O.4
Kim, W.B.5
-
84
-
-
36349033482
-
Phosphodiesterase type 5: Expanding roles in cardiovascular regulation
-
DOI 10.1161/CIRCRESAHA.107.162511, PII 0000301220071126000006
-
Kass DA, Champion HC, Beavo JA (2007) Phosphodiesterase type 5: expanding roles in cardiovascular regulation. Circ Res 101:1084-1095 (Pubitemid 350146434)
-
(2007)
Circulation Research
, vol.101
, Issue.11
, pp. 1084-1095
-
-
Kass, D.A.1
Champion, H.C.2
Beavo, J.A.3
-
85
-
-
70349320443
-
Structure, catalytic mechanism, and inhibitor selectivity of cyclic nucleotide phosphodiesterases
-
Beavo JA, Francis SH, Houslay MD (eds) Taylor & Francis Group, LLC, Boca Raton
-
Ke H, Wang EH (2007a) Structure, catalytic mechanism, and inhibitor selectivity of cyclic nucleotide phosphodiesterases. In: Beavo JA, Francis SH, Houslay MD (eds) Cyclic nucleotide phosphodiesterases in health and disease. Taylor & Francis Group, LLC, Boca Raton, pp 607-626
-
(2007)
Cyclic Nucleotide Phosphodiesterases in Health and Disease
, pp. 607-626
-
-
Ke, H.1
Wang, E.H.2
-
86
-
-
33847689816
-
Crystal structures of phosphodiesterases and implications on substrate specificity and inhibitor selectivity
-
DOI 10.2174/156802607779941242
-
Ke H, Wang H (2007b) Crystal structures of phosphodiesterases and implications on substrate specificity and inhibitor selectivity. Curr Top Med Chem 7:391-403 (Pubitemid 46358652)
-
(2007)
Current Topics in Medicinal Chemistry
, vol.7
, Issue.4
, pp. 391-403
-
-
Ke, H.1
Wang, H.2
-
87
-
-
77950287263
-
Cyclic nucleotide phosphodiesterases (PDE) and peptide motifs
-
Keravis T, Lugnier C (2010) Cyclic nucleotide phosphodiesterases (PDE) and peptide motifs. Curr Pharm Des 16(9):1114-1125
-
(2010)
Curr Pharm des
, vol.16
, Issue.9
, pp. 1114-1125
-
-
Keravis, T.1
Lugnier, C.2
-
88
-
-
0035818615
-
Upregulation of phosphodiesterase 1A1 expression is associated with the development of nitrate tolerance
-
Kim D, Rybalkin SD, Pi X, Wang Y, Zhang C, Munzel T, Beavo JA, Berk BC, Yan C (2001) Upregulation of phosphodiesterase 1A1 expression is associated with the development of nitrate tolerance. Circulation 104:2338-2343 (Pubitemid 33049518)
-
(2001)
Circulation
, vol.104
, Issue.19
, pp. 2338-2343
-
-
Kim, D.1
Rybalkin, S.D.2
Pi, X.3
Wang, Y.4
Zhang, C.5
Munzel, T.6
Beavo, J.A.7
Berk, B.C.8
Yan, C.9
-
89
-
-
0020564405
-
Dipyridamole inhibition of adenosine metabolism in human blood
-
DOI 10.1016/0014-2999(83)90026-2
-
Klabunde RE (1983) Dipyridamole inhibition of adenosine metabolism in human blood. Eur J Pharmacol 93:21-26 (Pubitemid 13005927)
-
(1983)
European Journal of Pharmacology
, vol.93
, Issue.1-2
, pp. 21-26
-
-
Klabunde, R.E.1
-
90
-
-
3142744558
-
Effect of low-dose theophylline on airway inflammation in COPD
-
DOI 10.1111/j.1440-1843.2004.00573.x
-
Kobayashi M, Nasuhara Y, Betsuyaku T, Shibuya E, Tanino Y, Tanino M, Takamura K, Nagai K, Hosokawa T, Nishimura M (2004) Effect of low-dose theophylline on airway inflammation in COPD. Respirology 9:249-254 (Pubitemid 38937400)
-
(2004)
Respirology
, vol.9
, Issue.2
, pp. 249-254
-
-
Kobayashi, M.1
Nasuhara, Y.2
Betsuyaku, T.3
Shibuya, E.4
Tanino, Y.5
Tanino, M.6
Takamura, K.7
Nagai, K.8
Hosokawa, T.9
Nishimura, M.10
-
91
-
-
0034733021
-
Conformational difference between PDE4 apoenzyme and holoenzyme
-
DOI 10.1021/bi992432w
-
Laliberte F, Han Y, Govindarajan A, Giroux A, Liu S, Bobechko B, Lario P, Bartlett A, Gorseth E, Gresser M, Huang Z (2000) Conformational difference between PDE4 apoenzyme and holoenzyme. Biochemistry 39:6449-6458 (Pubitemid 30347150)
-
(2000)
Biochemistry
, vol.39
, Issue.21
, pp. 6449-6458
-
-
Laliberte, F.1
Han, Y.2
Govindarajan, A.3
Giroux, A.4
Liu, S.5
Bobechko, B.6
Lario, P.7
Bartlett, A.8
Gorseth, E.9
Gresser, M.10
Huang, Z.11
-
92
-
-
0037070162
-
In vitro PKA phosphorylation-mediated human PDE4A4 activation
-
DOI 10.1016/S0014-5793(02)02259-7, PII S0014579302022597
-
Laliberte F, Liu S, Gorseth E, Bobechko B, Bartlett A, Lario P, Gresser MJ, Huang Z (2002) In vitro PKA phosphorylation-mediated human PDE4A4 activation. FEBS Lett 512:205-208 (Pubitemid 34164479)
-
(2002)
FEBS Letters
, vol.512
, Issue.1-3
, pp. 205-208
-
-
Laliberte, F.1
Liu, S.2
Gorseth, E.3
Bobechko, B.4
Bartlett, A.5
Lario, P.6
Gresser, M.J.7
Huang, Z.8
-
93
-
-
67650245968
-
Mdm2 directs the ubiquitination of barrestin-sequestered cAMP phosphodiesterase-4D5
-
Li X, Baillie GS, Houslay MD (2009) Mdm2 directs the ubiquitination of barrestin-sequestered cAMP phosphodiesterase-4D5. J Biol Chem 284:16170-16182
-
(2009)
J Biol Chem
, vol.284
, pp. 16170-16182
-
-
Li, X.1
Baillie, G.S.2
Houslay, M.D.3
-
94
-
-
0033538486
-
Activation of the cAMP-specific phosphodiesterase PDE4D3 by phosphorylation. Identification and function of an inhibitory domain
-
Lim J, Pahlke G, Conti M (1999) Activation of the cAMP-specific phosphodiesterase PDE4D3 by phosphorylation. Identification and function of an inhibitory domain. J Biol Chem 274:19677-19685
-
(1999)
J Biol Chem
, vol.274
, pp. 19677-19685
-
-
Lim, J.1
Pahlke, G.2
Conti, M.3
-
95
-
-
51649126214
-
Structural basis for the catalytic mechanism of human phosphodiesterase 9
-
Liu S, Mansour MN, Dillman KS, Perez JR, Danley DE, Aeed PA, Simons SP, Lemotte PK, Menniti FS (2008) Structural basis for the catalytic mechanism of human phosphodiesterase 9. Proc Natl Acad Sci USA 105:13309-13314
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 13309-13314
-
-
Liu, S.1
Mansour, M.N.2
Dillman, K.S.3
Perez, J.R.4
Danley, D.E.5
Aeed, P.A.6
Simons, S.P.7
Lemotte, P.K.8
Menniti, F.S.9
-
96
-
-
0025370222
-
Cloning and expression of cDNA for a human low-Km, rolipram-sensitive cyclic AMP phosphodiesterase
-
Livi GP, Kmetz P, McHale MM, Cieslinski LB, Sathe GM, Taylor DP, Davis RL, Torphy TJ, Balcarek JM (1990) Cloning and expression of cDNA for a human low-Km, rolipram-sensitive cyclic AMP phosphodiesterase. Mol Cell Biol 10:2678-2686
-
(1990)
Mol Cell Biol
, vol.10
, pp. 2678-2686
-
-
Livi, G.P.1
Kmetz, P.2
McHale, M.M.3
Cieslinski, L.B.4
Sathe, G.M.5
Taylor, D.P.6
Davis, R.L.7
Torphy, T.J.8
Balcarek, J.M.9
-
97
-
-
77950377332
-
Cardiac hypertrophy is not amplified by deletion of cGMP-dependent protein kinase i in cardiomyocytes
-
Lukowski R, Rybalkin SD, Loga F, Leiss V, Beavo JA, Hofmann F (2010) Cardiac hypertrophy is not amplified by deletion of cGMP-dependent protein kinase I in cardiomyocytes. Proc Natl Acad Sci USA 107:5646-5651
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 5646-5651
-
-
Lukowski, R.1
Rybalkin, S.D.2
Loga, F.3
Leiss, V.4
Beavo, J.A.5
Hofmann, F.6
-
98
-
-
23944494162
-
2-adrenergic receptor to activation of ERK in HEK293B2 cells
-
DOI 10.1074/jbc.M414316200
-
Lynch MJ, Baillie GS, Mohamed A, Li X, Maisonneuve C, Klussmann E, van Heeke G, Houslay MD (2005) RNA Silencing Identifies PDE4D5 as the Functionally Relevant cAMP Phosphodiesterase Interacting with {beta}Arrestin to Control the Protein Kinase A/AKAP79-mediated Switching of the {beta}2-Adrenergic Receptor to Activation of ERK in HEK293B2 Cells. J Biol Chem 280:33178-33189 (Pubitemid 41397113)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.39
, pp. 33178-33189
-
-
Lynch, M.J.1
Baillie, G.S.2
Mohamed, A.3
Li, X.4
Maisonneuve, C.5
Klussmann, E.6
Van Heeke, G.7
Houslay, M.D.8
-
99
-
-
0026032745
-
High concentrations of a cGMP-stimulated phosphodiesterase mediate ANP-induced decreases in cAMP and steroidogenesis in adrenal glomerulosa cells
-
MacFarland RT, Zelus BD, Beavo JA (1991) High concentrations of a cGMP-stimulated phosphodiesterase mediate ANP-induced decreases in cAMP and steroidogenesis in adrenal glomerulosa cells. J Biol Chem 266:136-142 (Pubitemid 21906101)
-
(1991)
Journal of Biological Chemistry
, vol.266
, Issue.1
, pp. 136-142
-
-
MacFarland, R.T.1
Zelus, B.D.2
Beavo, J.A.3
-
100
-
-
1642554150
-
GAF domains: Two billion year old molecular switches that bind cyclic nucleotides
-
Martinez SE, Beavo JA, Hol WG (2002a) GAF domains: two billion year old molecular switches that bind cyclic nucleotides. Mol Interv 2:317-323
-
(2002)
Mol Interv
, vol.2
, pp. 317-323
-
-
Martinez, S.E.1
Beavo, J.A.2
Hol, W.G.3
-
101
-
-
0036790852
-
The two GAF domains in phosphodiesterase 2A have distinct roles in dimerization and in cGMP binding
-
Martinez SE, Wu AY, Glavas NA, Tang XB, Turley S, Hol WG, Beavo JA (2002b) The two GAF domains in phosphodiesterase 2A have distinct roles in dimerization and in cGMP binding. Proc Natl Acad Sci USA 99:13260-13265
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 13260-13265
-
-
Martinez, S.E.1
Wu, A.Y.2
Glavas, N.A.3
Tang, X.B.4
Turley, S.5
Hol, W.G.6
Beavo, J.A.7
-
102
-
-
14544297871
-
Crystal structure of the tandem GAF domains from a cyanobacterial adenylyl cyclase: Modes of ligand binding and dimerization
-
DOI 10.1073/pnas.0409913102
-
Martinez SE, Bruder S, Schultz A, Zheng N, Schultz JE, Beavo JA, Linder JU (2005) Crystal structure of the tandem GAF domains from a cyanobacterial adenylyl cyclase: modes of ligand binding and dimerization. Proc Natl Acad Sci USA 102:3082-3087 (Pubitemid 40299919)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.8
, pp. 3082-3087
-
-
Martinez, S.E.1
Bruder, S.2
Schultz, A.3
Zheng, N.4
Schultz, J.E.5
Beavo, J.A.6
Linder, J.U.7
-
103
-
-
54449087235
-
The structure of the GAF A domain from phosphodiesterase 6C reveals determinants of cGMP binding, a conserved binding surface, and a large cGMP-dependent conformational change
-
Martinez SE, Heikaus CC, Klevit RE, Beavo JA (2008) The structure of the GAF A domain from phosphodiesterase 6C reveals determinants of cGMP binding, a conserved binding surface, and a large cGMP-dependent conformational change. J Biol Chem 283:25913-25919
-
(2008)
J Biol Chem
, vol.283
, pp. 25913-25919
-
-
Martinez, S.E.1
Heikaus, C.C.2
Klevit, R.E.3
Beavo, J.A.4
-
104
-
-
21644449363
-
In resting COS1 cells a dominant negative approach shows that specific, anchored PDE4 cAMP phosphodiesterase isoforms gate the activation, by basal cyclic AMP production, of AKAP-tethered protein kinase A type II located in the centrosomal region
-
DOI 10.1016/j.cellsig.2005.04.003, PII S0898656805000835
-
McCahill A, McSorley T, Huston E, Hill EV, Lynch MJ, Gall I, Keryer G, Lygren B, Tasken K, van Heeke G, Houslay MD (2005) In resting COS1 cells a dominant negative approach shows that specific, anchored PDE4 cAMP phosphodiesterase isoforms gate the activation, by basal cyclic AMP production, of AKAP-tethered protein kinase A type II located in the centrosomal region. Cell Signal 17:1158-1173 (Pubitemid 40933535)
-
(2005)
Cellular Signalling
, vol.17
, Issue.9
, pp. 1158-1173
-
-
McCahill, A.1
McSorley, T.2
Huston, E.3
Hill, E.V.4
Lynch, M.J.5
Gall, I.6
Keryer, G.7
Lygren, B.8
Tasken, K.9
Van Heeke, G.10
Houslay, M.D.11
-
105
-
-
0033597139
-
Association with the src family tyrosyl kinase LYN triggers a conformational change in the catalytic region of human cAMP-specific phosphodiesterase HSPDE4A4B: Consequences for rolipram inhibition
-
McPhee I, Yarwood SJ, Huston E, Scotland G, Beard MB, Ross AH, Houslay ES, Houslay MD (1999) Association with the src family tyrosyl kinase LYN triggers a conformational change in the catalytic region of human cAMP-specific phosphodiesterase HSPDE4A4B: consequences for rolipram inhibition. J Biol Chem 274:11796-11810
-
(1999)
J Biol Chem
, vol.274
, pp. 11796-11810
-
-
McPhee, I.1
Yarwood, S.J.2
Huston, E.3
Scotland, G.4
Beard, M.B.5
Ross, A.H.6
Houslay, E.S.7
Houslay, M.D.8
-
106
-
-
0029074582
-
Erythro-9-(2-hydroxy-3-nonyl) adenine inhibits cyclic GMP-stimulated phosphodiesterase in isolated cardiac myocytes
-
Mery PF, Pavoine C, Pecker F, Fischmeister R (1995) Erythro-9-(2-hydroxy- 3-nonyl) adenine inhibits cyclic GMP-stimulated phosphodiesterase in isolated cardiac myocytes. Mol Pharmacol 48:121-130
-
(1995)
Mol Pharmacol
, vol.48
, pp. 121-130
-
-
Mery, P.F.1
Pavoine, C.2
Pecker, F.3
Fischmeister, R.4
-
107
-
-
72449174812
-
Role of Ca2+/calmodulinstimulated cyclic nucleotide phosphodiesterase 1 in mediating cardiomyocyte hypertrophy
-
Miller CL, Oikawa M, Cai Y, Wojtovich AP, Nagel DJ, Xu X, Xu H, Florio V, Rybalkin SD, Beavo JA, Chen YF, Li JD, Blaxall BC, Abe J, Yan C (2009) Role of Ca2+/calmodulinstimulated cyclic nucleotide phosphodiesterase 1 in mediating cardiomyocyte hypertrophy. Circ Res 105:956-964
-
(2009)
Circ Res
, vol.105
, pp. 956-964
-
-
Miller, C.L.1
Oikawa, M.2
Cai, Y.3
Wojtovich, A.P.4
Nagel, D.J.5
Xu, X.6
Xu, H.7
Florio, V.8
Rybalkin, S.D.9
Beavo, J.A.10
Chen, Y.F.11
Li, J.D.12
Blaxall, B.C.13
Abe, J.14
Yan, C.15
-
108
-
-
3142723295
-
Fluorescence resonance energy transfer-based analysis of cAMP dynamics in live neonatal rat cardiac myocytes reveals distinct functions of compartmentalized phosphodiesterases
-
DOI 10.1161/01.RES.0000134629.84732.11
-
Mongillo M, McSorley T, Evellin S, Sood A, Lissandron V, Terrin A, Huston E, Hannawacker A, Lohse MJ, Pozzan T, Houslay MD, ZaccoloM(2004) Fluorescence resonance energy transferbased analysis of cAMP dynamics in live neonatal rat cardiac myocytes reveals distinct functions of compartmentalized phosphodiesterases. Circ Res 95:67-75 (Pubitemid 38931837)
-
(2004)
Circulation Research
, vol.95
, Issue.1
, pp. 67-75
-
-
Mongillo, M.1
McSorley, T.2
Evellin, S.3
Sood, A.4
Lissandron, V.5
Terrin, A.6
Huston, E.7
Hannawacker, A.8
Lohse, M.J.9
Pozzan, T.10
Houslay, M.D.11
Zaccolo, M.12
-
109
-
-
33644865929
-
Compartmentalised phosphodiesterase-2 (PDE2) activity blunts b-adrenergic cardiac inotropy via a b3-adrenoceptor/NO/cGMP dependent pathway
-
Mongillo M, Tocchetti CG, Terrin A, Lissandron V, Cheung Y-F, Dostmann WR, Pozzan T, Kass DA, Paolocci N, Houslay MD, Zaccolo M (2006) Compartmentalised phosphodiesterase-2 (PDE2) activity blunts b-adrenergic cardiac inotropy via a b3-adrenoceptor/NO/cGMP dependent pathway. Circ Res 98:226-234
-
(2006)
Circ Res
, vol.98
, pp. 226-234
-
-
Mongillo, M.1
Tocchetti, C.G.2
Terrin, A.3
Lissandron, V.4
Cheung, Y.-F.5
Dostmann, W.R.6
Pozzan, T.7
Kass, D.A.8
Paolocci, N.9
Houslay, M.D.10
Zaccolo, M.11
-
110
-
-
5644251010
-
Inhibition of Phosphodiesterase Type 5 by the Activator of Nitric Oxide-Sensitive Guanylyl Cyclase BAY 41-2272
-
DOI 10.1161/01.CIR.0000126286.47618.BD
-
Mullershausen F, Russwurm M, Friebe A, Koesling D (2004) Inhibition of phosphodiesterase type 5 by the activator of nitric oxide-sensitive guanylyl cyclase BAY 41-2272. Circulation 109:1711-1713 (Pubitemid 38500670)
-
(2004)
Circulation
, vol.109
, Issue.14
, pp. 1711-1713
-
-
Mullershausen, F.1
Russwurm, M.2
Friebe, A.3
Koesling, D.4
-
111
-
-
34548389858
-
Isoform-selective susceptibility of DISC1/phosphodiesterase-4 complexes to dissociation by elevated intracellular cAMP levels
-
DOI 10.1523/JNEUROSCI.1493-07.2007
-
Murdoch H, Mackie S, Collins DM, Hill EV, Bolger GB, Klussmann E, Porteous DJ, Millar JK, Houslay MD (2007) Isoform-selective susceptibility of DISC1/phosphodiesterase-4 complexes to dissociation by elevated intracellular cAMP levels. J Neurosci 27:9513-9524 (Pubitemid 47358203)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.35
, pp. 9513-9524
-
-
Murdoch, H.1
Mackie, S.2
Collins, D.M.3
Hill, E.V.4
Bolger, G.B.5
Klussmann, E.6
Porteous, D.J.7
Millar, J.K.8
Houslay, M.D.9
-
112
-
-
47949087086
-
Sustained soluble guanylate cyclase stimulation offsets nitric-oxide synthase inhibition to restore acute cardiac modulation by sildenafil
-
Nagayama T, Zhang M, Hsu S, Takimoto E, Kass DA (2008) Sustained soluble guanylate cyclase stimulation offsets nitric-oxide synthase inhibition to restore acute cardiac modulation by sildenafil. J Pharmacol Exp Ther 326:380-387
-
(2008)
J Pharmacol Exp Ther
, vol.326
, pp. 380-387
-
-
Nagayama, T.1
Zhang, M.2
Hsu, S.3
Takimoto, E.4
Kass, D.A.5
-
113
-
-
0027244894
-
The cDNA of a human lymphocyte cyclic-AMP phosphodiesterase (PDE IV) reveals a multigene family
-
Obernolte R, Bhakta S, Alvarez R, Bach C, Zuppan P, Mulkins M, Jarnagin K, Shelton ER (1993) The cDNA of a human lymphocyte cyclic-AMP phosphodiesterase (PDE IV) reveals a multigene family. Gene 129:239-247
-
(1993)
Gene
, vol.129
, pp. 239-247
-
-
Obernolte, R.1
Bhakta, S.2
Alvarez, R.3
Bach, C.4
Zuppan, P.5
Mulkins, M.6
Jarnagin, K.7
Shelton, E.R.8
-
115
-
-
0031719432
-
Critical role of conserved histidine pairs HNXXH and HDXXH in recombinant human phosphodiesterase 4A
-
DOI 10.1016/S0898-6568(97)00175-7, PII S0898656897001757
-
Omburo GA, Jacobitz S, Torphy TJ, Colman RW (1998) Critical role of conserved histidine pairs HNXXH and HDXXH in recombinant human phosphodiesterase 4A. Cell Signal 10:491-497 (Pubitemid 28404433)
-
(1998)
Cellular Signalling
, vol.10
, Issue.7
, pp. 491-497
-
-
Omburo, G.A.1
Jacobitz, S.2
Torphy, T.J.3
Colman, R.W.4
-
116
-
-
77950194782
-
PDE11
-
Beavo JA, Francis SH, Houslay MD (eds) CRC Press, Boca Raton
-
Omori K, Kotera J (2006) PDE11. In: Beavo JA, Francis SH, Houslay MD (eds) Cyclic nucleotide phosphodiesterases in health and disease. CRC Press, Boca Raton, pp 255-274
-
(2006)
Cyclic Nucleotide Phosphodiesterases in Health and Disease
, pp. 255-274
-
-
Omori, K.1
Kotera, J.2
-
117
-
-
33847068206
-
Overview of PDEs and their regulation
-
Omori K, Kotera J (2007) Overview of PDEs and their regulation. Circ Res 100:309-327
-
(2007)
Circ Res
, vol.100
, pp. 309-327
-
-
Omori, K.1
Kotera, J.2
-
118
-
-
67649946944
-
Identification, synthesis and SAR of amino substituted pyrido[3, 2b]pyrazinones as potent and selective PDE5 inhibitors
-
Owen DR, Walker JK, Jon Jacobsen E, Freskos JN, Hughes RO, Brown DL, Bell AS, Brown DG, Phillips C, Mischke BV, Molyneaux JM, Fobian YM, Heasley SE, Moon JB, Stallings WC, Joseph Rogier D, Fox DN, Palmer MJ, Ringer T, Rodriquez-Lens M, Cubbage JW, Blevis-Bal RM, Benson AG, Acker BA, Maddux TM, Tollefson MB, Bond BR, Macinnes A, Yu Y (2009) Identification, synthesis and SAR of amino substituted pyrido[3, 2b]pyrazinones as potent and selective PDE5 inhibitors. Bioorg Med Chem Lett 19:4088-4091
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 4088-4091
-
-
Owen, D.R.1
Walker, J.K.2
Jon Jacobsen, E.3
Freskos, J.N.4
Hughes, R.O.5
Brown, D.L.6
Bell, A.S.7
Brown, D.G.8
Phillips, C.9
Mischke, B.V.10
Molyneaux, J.M.11
Fobian, Y.M.12
Heasley, S.E.13
Moon, J.B.14
Stallings, W.C.15
Joseph Rogier, D.16
Fox, D.N.17
Palmer, M.J.18
Ringer, T.19
Rodriquez-Lens, M.20
Cubbage, J.W.21
Blevis-Bal, R.M.22
Benson, A.G.23
Acker, B.A.24
Maddux, T.M.25
Tollefson, M.B.26
Bond, B.R.27
MacInnes, A.28
Yu, Y.29
more..
-
119
-
-
70849084890
-
Mechanism for the allosteric regulation of phosphodiesterase 2A deduced from the X-ray structure of a near full-length construct
-
Pandit J, Forman MD, Fennell KF, Dillman KS, Menniti FS (2009) Mechanism for the allosteric regulation of phosphodiesterase 2A deduced from the X-ray structure of a near full-length construct. Proc Natl Acad Sci USA 106:18225-18230
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 18225-18230
-
-
Pandit, J.1
Forman, M.D.2
Fennell, K.F.3
Dillman, K.S.4
Menniti, F.S.5
-
120
-
-
77949472038
-
Compartmentalized cyclic adenosine 30, 50-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains
-
Penmatsa H, Zhang W, Yarlagadda S, Li C, Conoley VG, Yue J, Bahouth SW, Buddington RK, Zhang G, Nelson DJ, Sonecha MD, Manganiello V, Wine JJ, Naren AP (2010) Compartmentalized cyclic adenosine 30, 50-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains. Mol Biol Cell 21:1097-1110
-
(2010)
Mol Biol Cell
, vol.21
, pp. 1097-1110
-
-
Penmatsa, H.1
Zhang, W.2
Yarlagadda, S.3
Li, C.4
Conoley, V.G.5
Yue, J.6
Bahouth, S.W.7
Buddington, R.K.8
Zhang, G.9
Nelson, D.J.10
Sonecha, M.D.11
Manganiello, V.12
Wine, J.J.13
Naren, A.P.14
-
121
-
-
41449112813
-
Cyclic nucleotide analogs as probes of signaling pathways [1]
-
DOI 10.1038/nmeth0408-277, PII NMETH0408-277
-
Poppe H, Rybalkin SD, Rehmann H, Hinds TR, Tang XB, Christensen AE, Schwede F, Genieser HG, Bos JL, Doskeland SO, Beavo JA, Butt E (2008) Cyclic nucleotide analogs as probes of signaling pathways. Nat Methods 5:277-278 (Pubitemid 351455143)
-
(2008)
Nature Methods
, vol.5
, Issue.4
, pp. 277-278
-
-
Poppe, H.1
Rybalkin, S.D.2
Rehmann, H.3
Hinds, T.R.4
Tang, X.-B.5
Christensen, A.E.6
Schwede, F.7
Genieser, H.-G.8
Bos, J.L.9
Doskeland, S.O.10
Beavo, J.A.11
Butt, E.12
-
122
-
-
65549120682
-
Interaction of phosphodiesterase 3 Awithbrefeldin A-inhibited guaninenucleotide-exchangeproteins BIG1 and BIG2 and effect on ARF1 activity
-
Puxeddu E, Uhart M, Li CC, Ahmad F, Pacheco-Rodriguez G, Manganiello VC, Moss J, Vaughan M (2009) Interaction of phosphodiesterase 3 Awithbrefeldin A-inhibited guaninenucleotide-exchangeproteins BIG1 and BIG2 and effect on ARF1 activity. Proc Natl AcadSci USA 106: 6158-6163
-
(2009)
Proc Natl AcadSci USA
, vol.106
, pp. 6158-6163
-
-
Puxeddu, E.1
Uhart, M.2
Li, C.C.3
Ahmad, F.4
Pacheco-Rodriguez, G.5
Manganiello, V.C.6
Moss, J.7
Vaughan, M.8
-
123
-
-
0029072842
-
Theophylline and selective PDE inhibitors as bronchodilators and smooth muscle relaxants
-
Rabe KF, Magnussen H, Dent G (1995) Theophylline and selective PDE inhibitors as bronchodilators and smooth muscle relaxants. Eur Respir J 8:637-642
-
(1995)
Eur Respir J
, vol.8
, pp. 637-642
-
-
Rabe, K.F.1
Magnussen, H.2
Dent, G.3
-
124
-
-
0035818473
-
A uniform extracellular stimulus triggers distinct cAMP signals in different compartments of a simple cell
-
DOI 10.1073/pnas.221381398
-
Rich TC, Fagan KA, Tse TE, Schaack J, Cooper DM, Karpen JW (2001a) A uniform extracellular stimulus triggers distinct cAMP signals in different compartments of a simple cell. Proc Natl Acad Sci USA 98:13049-13054 (Pubitemid 33051315)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.23
, pp. 13049-13054
-
-
Rich, T.C.1
Fagan, K.A.2
Tse, T.E.3
Schaack, J.4
Cooper, D.M.F.5
Karpen, J.W.6
-
125
-
-
0034942107
-
In vivo assessment of local phosphodiesterase activity using tailored cyclic nucleotide-gated channels as cAMP sensors
-
Rich TC, Tse TE, Rohan JG, Schaack J, Karpen JW (2001b) In vivo assessment of local phosphodiesterase activity using tailored cyclic nucleotide-gated channels as cAMP sensors. J Gen Physiol 118:63-78
-
(2001)
J Gen Physiol
, vol.118
, pp. 63-78
-
-
Rich, T.C.1
Tse, T.E.2
Rohan, J.G.3
Schaack, J.4
Karpen, J.W.5
-
126
-
-
33846305048
-
Cellular mechanisms underlying prostaglandin-induced transient cAMP signals near the plasma membrane of HEK-293 cells
-
DOI 10.1152/ajpcell.00121.2006
-
Rich TC, Xin W, Mehats C, Hassell KA, Piggott L, Le X, Karpen JW, Conti M (2006) Cellular mechanisms underlying prostaglandin-induced transient cAMP signals near the plasma membrane of HEK-293 cells. Am J Physiol Cell Physiol 292:C319-C331 (Pubitemid 46115141)
-
(2007)
American Journal of Physiology - Cell Physiology
, vol.292
, Issue.1
-
-
Rich, T.C.1
Xin, W.2
Mehats, C.3
Hassell, K.A.4
Piggott, L.A.5
Le, X.6
Karpen, J.W.7
Conti, M.8
-
127
-
-
0037174825
-
Dimerization of the type 4 cAMP-specific phosphodiesterases is mediated by the upstream conserved regions (UCRs)
-
DOI 10.1074/jbc.M203585200
-
Richter W, Conti M (2002) Dimerization of the type 4 cAMP-specific phosphodiesterases is mediated by the upstream conserved regions (UCRs). J Biol Chem 277:40212-40221 (Pubitemid 35215591)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.43
, pp. 40212-40221
-
-
Richter, W.1
Conti, M.2
-
128
-
-
3142776354
-
The oligomerization state determines regulatory properties and inhibitor sensitivity of type 4 cAMP-specific phosphodiesterases
-
DOI 10.1074/jbc.M312687200
-
Richter W, ContiM(2004) The oligomerization state determines regulatory properties and inhibitor sensitivityoftype4cAMP-specificphosphodiesterases. JBiolChem279:30338-30348 (Pubitemid 38937961)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.29
, pp. 30338-30348
-
-
Richter, W.1
Conti, M.2
-
129
-
-
0031105672
-
Detailed characterization of a purified type 4 phosphodiesterase, HSPDE4B2B: Differentiation of high- and low-affinity (R)-rolipram binding
-
DOI 10.1006/prep.1996.0683
-
Rocque WJ, Holmes WD, Patel IR, Dougherty RW, Ittoop O, Overton L, Hoffman CR, Wisely GB, Willard DH, Luther MA (1997) Detailed characterization of a purified type 4 phosphodiesterase, HSPDE4B2B: differentiation of high-and low-affinity (R)-rolipram binding. Protein Exp Purif 9:191-202 (Pubitemid 27210714)
-
(1997)
Protein Expression and Purification
, vol.9
, Issue.2
, pp. 191-202
-
-
Rocque, W.J.1
Holmes, W.D.2
Patel, I.R.3
Dougherty, R.W.4
Ittoop, O.5
Overton, L.6
Hoffman, C.R.7
Wisely, G.B.8
Willard, D.H.9
Luther, M.A.10
-
130
-
-
0030831875
-
Calmodulin-stimulated cyclic nucleotide phosphodiesterase (PDE1C) is induced in human arterial smooth muscle cells of the synthetic, proliferative phenotype
-
Rybalkin SD, Bornfeldt KE, Sonnenburg WK, Rybalkina IG, Kwak KS, Hanson K, Krebs EG, Beavo JA (1997) Calmodulin-stimulated cyclic nucleotide phosphodiesterase (PDE1C) is induced in human arterial smooth muscle cells of the synthetic, proliferative phenotype. J Clin Invest 100:2611-2621 (Pubitemid 27514902)
-
(1997)
Journal of Clinical Investigation
, vol.100
, Issue.10
, pp. 2611-2621
-
-
Rybalkin, S.D.1
Bornfeldt, K.E.2
Sonnenburg, W.K.3
Rybalkina, I.G.4
Kwak, K.S.5
Hanson, K.6
Krebs, E.G.7
Beavo, J.A.8
-
131
-
-
0042859823
-
Cyclic GMP phosphodiesterases and regulation of smooth muscle function
-
DOI 10.1161/01.RES.0000087541.15600.2B
-
Rybalkin SD, Yan C, Bornfeldt KE, Beavo JA (2003) Cyclic GMP phosphodiesterases and regulation of smooth muscle function. Circ Res 93:280-291 (Pubitemid 37048240)
-
(2003)
Circulation Research
, vol.93
, Issue.4
, pp. 280-291
-
-
Rybalkin, S.D.1
Yan, C.2
Bornfeldt, K.E.3
Beavo, J.A.4
-
132
-
-
77950223491
-
Multiple affinity states of cGMP-specific phosphodiesterase for sildenafil inhibition defined by cGMP-dependent and cGMP-independent mechanisms
-
Rybalkina IG, Tang XB, Rybalkin SD (2010) Multiple affinity states of cGMP-specific phosphodiesterase for sildenafil inhibition defined by cGMP-dependent and cGMP-independent mechanisms. Mol Pharmacol 77:670-677
-
(2010)
Mol Pharmacol
, vol.77
, pp. 670-677
-
-
Rybalkina, I.G.1
Tang, X.B.2
Rybalkin, S.D.3
-
133
-
-
0031712906
-
Heterologous expression and purification of recombinant rolipram-sensitive cyclic AMP-specific phosphodiesterases
-
Salanova M, Jin SC, Conti M (1998) Heterologous expression and purification of recombinant rolipram-sensitive cyclic AMP-specific phosphodiesterases. Methods 14:55-64
-
(1998)
Methods
, vol.14
, pp. 55-64
-
-
Salanova, M.1
Jin, S.C.2
Conti, M.3
-
134
-
-
0031606166
-
Purification and Physical Characterization of Cloned Human cAMP Phosphodiesterases PDE-4D and -4C
-
Saldou N, Baecker PA, Li B, Yuan Z, Obernolte R, Ratzliff J, Osen E, Jarnagin K, Shelton ER (1998) Purification and physical characterization of cloned human cAMP phosphodiesterases PDE-4D and -4C. Cell Biochem Biophys 28:187-217 (Pubitemid 128533776)
-
(1998)
Cell Biochemistry and Biophysics
, vol.28
, Issue.2-3
, pp. 187-217
-
-
Saldou, N.1
Baecker, P.A.2
Li, B.3
Yuan, Z.4
Obernolte, R.5
Ratzliff, J.6
Osen, E.7
Jarnagin, K.8
Shelton, E.R.9
-
135
-
-
2442700405
-
Crystal structure of human phosphodiesterase 3B: Atomic basis for substrate and inhibitor specificity
-
DOI 10.1021/bi049868i
-
Scapin G, Patel SB, Chung C, Varnerin JP, Edmondson SD, Mastracchio A, Parmee ER, Singh SB, Becker JW, Van der Ploeg LH, Tota MR (2004) Crystal structure of human phosphodiesterase 3B: atomic basis for substrate and inhibitor specificity. Biochemistry 43:6091-6100 (Pubitemid 38669477)
-
(2004)
Biochemistry
, vol.43
, Issue.20
, pp. 6091-6100
-
-
Scapin, G.1
Patel, S.B.2
Chung, C.3
Varnerin, J.P.4
Edmondson, S.D.5
Mastracchio, A.6
Parmee, E.R.7
Singh, S.B.8
Becker, J.W.9
Van Der Ploeg, L.H.T.10
Tota, M.R.11
-
136
-
-
29744448378
-
Dipyridamole, an underestimated vascular protective drug
-
DOI 10.1007/s10557-005-4659-6
-
Schaper W (2005) Dipyridamole, an underestimated vascular protective drug. Cardiovasc Drugs Ther 19:357-363 (Pubitemid 43029821)
-
(2005)
Cardiovascular Drugs and Therapy
, vol.19
, Issue.5
, pp. 357-363
-
-
Schaper, W.1
-
137
-
-
79960910019
-
The GAF-tandem domain of phosphodiesterase 5 as a potential drug target
-
Francis SH, Conti M, Houslay MD (eds) Springer, Heidelberg
-
Schultz JE, Dunkern T, Gawlitta-Gorka E, Sorg G (2011) The GAF-tandem domain of phosphodiesterase 5 as a potential drug target. Francis SH, Conti M, HouslayMD (eds) Phosphodiesterases as drug targets. Springer, Heidelberg
-
(2011)
Phosphodiesterases As Drug Targets
-
-
Schultz, J.E.1
Dunkern, T.2
Gawlitta-Gorka, E.3
Sorg, G.4
-
138
-
-
0029008078
-
Chimeric constructs show that the unique N-terminal domain of the cyclic AMP phosphodiesterase RD1 (rPDE-IVA1;RNPDE4A1A) can confer membrane association upon the normally cytosolic protein chloramphenicol acetyl transferase (CAT)
-
Scotland G, Houslay MD (1995) Chimeric constructs show that the unique N-terminal domain of the cyclic AMP phosphodiesterase RD1 (rPDE-IVA1;RNPDE4A1A) can confer membrane association upon the normally cytosolic protein chloramphenicol acetyl transferase (CAT). Biochem J 308:673-681
-
(1995)
Biochem J
, vol.308
, pp. 673-681
-
-
Scotland, G.1
Houslay, M.D.2
-
139
-
-
0002994013
-
Design and synthesis of xanthines and cyclic GMP analogues as potent inhibitors of PDE5
-
Schudt C, Dent G, Rabe KF (eds) Academic, New York
-
Sekhar KR, Grondin P, Francis SH, Corbin JD (1996) Design and synthesis of xanthines and cyclic GMP analogues as potent inhibitors of PDE5. In: Schudt C, Dent G, Rabe KF (eds) Phosphodiesterase inhibitors. Academic, New York, pp 135-146
-
(1996)
Phosphodiesterase Inhibitors
, pp. 135-146
-
-
Sekhar, K.R.1
Grondin, P.2
Francis, S.H.3
Corbin, J.D.4
-
140
-
-
70449381345
-
Distribution of dipyridamole in blood components among post-stroke patients treated with extended release formulation
-
Serebruany V, Sabaeva E, Booze C, Atar OD, Eisert C, Hanley D (2009) Distribution of dipyridamole in blood components among post-stroke patients treated with extended release formulation. Thromb Haemost 102:538-543
-
(2009)
Thromb Haemost
, vol.102
, pp. 538-543
-
-
Serebruany, V.1
Sabaeva, E.2
Booze, C.3
Atar, O.D.4
Eisert, C.5
Hanley, D.6
-
141
-
-
0030006920
-
Phosphorylation and activation of a cAMP-specific phosphodiesterase by the cAMP-dependent protein kinase. Involvement of serine 54 in the enzyme activation
-
DOI 10.1074/jbc.271.28.16526
-
Sette C, Conti M (1996) Phosphorylation and activation of a cAMP-specific phosphodiesterase by the cAMP-dependent protein kinase. Involvement of serine 54 in the enzyme activation. J Biol Chem 271:16526-16534 (Pubitemid 26239006)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.28
, pp. 16526-16534
-
-
Sette, C.1
Conti, M.2
-
142
-
-
0027295333
-
Engineered deletion of the unique N-terminal domain of the cyclic AMP-specific phosphodiesterase RD1 prevents plasma membrane association and the attainment of enhanced thermostability without altering its sensitivity to inhibition by rolipram
-
Shakur Y, Pryde J, Houslay MD (1993) Engineered deletion of the unique N-terminal domain of the cyclic AMP specific phosphodiesterase RD1 prevents plasma membrane association and the attainment of enhanced thermostability without altering its sensitivity to inhibition by rolipram. Biochem J 292:677-686 (Pubitemid 23210195)
-
(1993)
Biochemical Journal
, vol.292
, Issue.3
, pp. 677-686
-
-
Shakur, Y.1
Pryde, J.G.2
Houslay, M.D.3
-
143
-
-
8944228921
-
1H NMR and identification of the membrane association domain using chimeric constructs
-
DOI 10.1074/jbc.271.28.16703
-
Smith KJ, Scotland G, Beattie J, Trayer IP, Houslay MD (1996) Determination of the structure of the N-terminal splice region of the cyclic AMP-specific phosphodiesterase RD1 (RNPDE4A1) by 1H-NMR and identification of the membrane association domain using chimeric constructs. J Biol Chem 271:16703-16711 (Pubitemid 26239033)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.28
, pp. 16703-16711
-
-
John Smith, K.1
Scotland, G.2
Beattie, J.3
Trayer, I.P.4
Houslay, M.D.5
-
144
-
-
35148892803
-
1H NMR structural and functional characterisation of a cAMP-specific phosphodiesterase-4D5 (PDE4D5) N-terminal region peptide that disrupts PDE4D5 interaction with the signalling scaffold proteins, βarrestin and RACK1
-
DOI 10.1016/j.cellsig.2007.08.015, PII S0898656807002653
-
Smith KJ, Baillie GS, Hyde EI, Li X, Houslay TM, McCahill A, Dunlop AJ, Bolger GB, Klussmann E, Adams DR, Houslay MD (2007) 1H NMR structural and functional characterisation of a cAMP-specific phosphodiesterase-4D5 (PDE4D5) N-terminal region peptide that disrupts PDE4D5 interaction with the signalling scaffold proteins, beta-arrestin and RACK1. Cell Signal 19:2612-2624 (Pubitemid 47542301)
-
(2007)
Cellular Signalling
, vol.19
, Issue.12
, pp. 2612-2624
-
-
Smith, K.J.1
Baillie, G.S.2
Hyde, E.I.3
Li, X.4
Houslay, T.M.5
McCahill, A.6
Dunlop, A.J.7
Bolger, G.B.8
Klussmann, E.9
Adams, D.R.10
Houslay, M.D.11
-
145
-
-
0030925148
-
Proposal for pharmacologically distinct conformers of PDE4 cyclic AMP phosphodiesterases
-
DOI 10.1016/S0898-6568(96)00173-8, PII S0898656896001738
-
Souness JE, Rao S (1997) Proposal for pharmacologically distinct conformers of PDE4 cyclic AMP phosphodiesterases. Cell Signal 9:227-236 (Pubitemid 27271642)
-
(1997)
Cellular Signalling
, vol.9
, Issue.3-4
, pp. 227-236
-
-
Souness, J.E.1
Rao, S.2
-
146
-
-
61749096117
-
NO-independent, haem-dependent soluble guanylate cyclase stimulators
-
Stasch JP, Hobbs AJ (2009) NO-independent, haem-dependent soluble guanylate cyclase stimulators. Handb Exp Pharmacol 191:277-308
-
(2009)
Handb Exp Pharmacol
, vol.191
, pp. 277-308
-
-
Stasch, J.P.1
Hobbs, A.J.2
-
147
-
-
0035029169
-
Compartmentation of G protein-coupled signaling pathways in cardiac myocytes
-
DOI 10.1146/annurev.pharmtox.41.1.751
-
Steinberg SF, Brunton LL (2001) Compartmentation of G protein-coupled signaling pathways in cardiac myocytes. Annu Rev Pharmacol Toxicol 41:751-773 (Pubitemid 32385905)
-
(2001)
Annual Review of Pharmacology and Toxicology
, vol.41
, pp. 751-773
-
-
Steinberg, S.F.1
Brunton, L.L.2
-
148
-
-
0033985281
-
Potent effects of novel anti-platelet aggregatory cilostamide analogues on recombinant cyclic nucleotide phosphodiesterase isozyme activity
-
DOI 10.1016/S0006-2952(99)00346-9, PII S0006295299003469
-
Sudo T, Tachibana K, Toga K, Tochizawa S, Inoue Y, Kimura Y, Hidaka H (2000) Potent effects of novel anti-platelet aggregatory cilostamide analogues on recombinant cyclic nucleotide phosphodiesterase isozyme activity. Biochem Pharmacol 59:347-356 (Pubitemid 30015963)
-
(2000)
Biochemical Pharmacology
, vol.59
, Issue.4
, pp. 347-356
-
-
Sudo, T.1
Tachibana, K.2
Toga, K.3
Tochizawa, S.4
Inoue, Y.5
Kimura, Y.6
Hidaka, H.7
-
149
-
-
0028004238
-
Molecular cloning and expression, in both COS-1 cells and S. cerevisiae, of a human cytosolic type-IVA, cyclic AMP specific phosphodiesterase (hPDE-IVA-h6.1)
-
Sullivan M, Egerton M, Shakur Y, Marquardsen A, Houslay MD (1994) Molecular cloning and expression, in both COS-1 cells and S. cerevisiae, of a human cytosolic type-IVA, cyclic AMP specific phosphodiesterase (hPDE-IVA-h6.1). Cell Signal 6:793-812
-
(1994)
Cell Signal
, vol.6
, pp. 793-812
-
-
Sullivan, M.1
Egerton, M.2
Shakur, Y.3
Marquardsen, A.4
Houslay, M.D.5
-
150
-
-
0041321268
-
Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules
-
DOI 10.1038/nature01914
-
Sung BJ, Hwang KY, Jeon YH, Lee JI, Heo YS, Kim JH, Moon J, Yoon JM, Hyun YL, Kim E, Eum SJ, Park SY, Lee JO, Lee TG, Ro S, Cho JM (2003) Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules. Nature 425:98-102 (Pubitemid 37101725)
-
(2003)
Nature
, vol.425
, Issue.6953
, pp. 98-102
-
-
Sung, B.-J.1
Hwang, K.Y.2
Jeon, Y.H.3
Lee, J.I.4
Heo, Y.-S.5
Kim, J.H.6
Moon, J.7
Yoon, J.M.8
Hyun, Y.-L.9
Kim, E.10
Eum, S.J.11
Park, S.-Y.12
Lee, J.-O.13
Lee, T.G.14
Ro, S.15
Cho, J.M.16
-
151
-
-
19944428363
-
CGMP catabolism by phosphodiesterase 5A regulates cardiac adrenergic stimulation by NOS3-dependent mechanism
-
DOI 10.1161/01.RES.0000152262.22968.72
-
Takimoto E, Champion HC, Belardi D, Moslehi J, Mongillo M, Mergia E, Montrose DC, Isoda T, Aufiero K, Zaccolo M, Dostmann WR, Smith CJ, Kass DA (2005a) cGMP catabolism by phosphodiesterase 5A regulates cardiac adrenergic stimulation by NOS3-dependent mechanism. Circ Res 96:100-109 (Pubitemid 40095759)
-
(2005)
Circulation Research
, vol.96
, Issue.1
, pp. 100-109
-
-
Takimoto, E.1
Champion, H.C.2
Belardi, D.3
Moslehi, J.4
Mongillo, M.5
Mergia, E.6
Montrose, D.C.7
Isoda, T.8
Aufiero, K.9
Zaccolo, M.10
Dostmann, W.R.11
Smith, C.J.12
Kass, D.A.13
-
152
-
-
20044363270
-
Chronic inhibition of cyclic GMP phosphodiesterase 5A prevents and reverses cardiac hypertrophy
-
DOI 10.1038/nm1175
-
Takimoto E, Champion HC, Li M, Belardi D, Ren S, Rodriguez ER, Bedja D, Gabrielson KL, Wang Y, Kass DA (2005b) Chronic inhibition of cyclic GMP phosphodiesterase 5A prevents and reverses cardiac hypertrophy. Nat Med 11:214-222 (Pubitemid 40321358)
-
(2005)
Nature Medicine
, vol.11
, Issue.2
, pp. 214-222
-
-
Takimoto, E.1
Champion, H.C.2
Li, M.3
Belardi, D.4
Ren, S.5
Rodriguez, E.R.6
Bedja, D.7
Gabrielson, K.L.8
Wang, Y.9
Kass, D.A.10
-
153
-
-
33748314488
-
Zaprinast, a well-known cyclic guanosine monophosphate-specific phosphodiesterase inhibitor, is an agonist for GPR35
-
DOI 10.1016/j.febslet.2006.08.015, PII S0014579306009756
-
Taniguchi Y, Tonai-Kachi H, Shinjo K (2006) Zaprinast, a well-known cyclic guanosine monophosphate-specific phosphodiesterase inhibitor, is an agonist for GPR35. FEBS Lett 580:5003-5008 (Pubitemid 44332369)
-
(2006)
FEBS Letters
, vol.580
, Issue.21
, pp. 5003-5008
-
-
Taniguchi, Y.1
Tonai-Kachi, H.2
Shinjo, K.3
-
154
-
-
0035933817
-
Phosphodiesterase 4D and protein kinase a type II constitute a signaling unit in the centrosomal area
-
Tasken KA, Collas P, Kemmner WA, Witczak O, Conti M, Tasken K (2001) Phosphodiesterase 4D and protein kinase a type II constitute a signaling unit in the centrosomal area. J Biol Chem 276:21999-22002
-
(2001)
J Biol Chem
, vol.276
, pp. 21999-22002
-
-
Tasken, K.A.1
Collas, P.2
Kemmner, W.A.3
Witczak, O.4
Conti, M.5
Tasken, K.6
-
155
-
-
79960905531
-
Pharmacology, clinical efficacy and tolerability of PDE4 inhibitors: Impact of human pharmacokinetics
-
Francis SH, Conti M, Houslay MD (eds) Springer, Heidelberg
-
Tenor H, Hatzelmann A, Beume R, Lahu G, Zech K, Bethke TD (2011) Pharmacology, clinical efficacy and tolerability of PDE4 inhibitors: Impact of human pharmacokinetics. Francis SH, Conti M, HouslayMD (eds) Phosphodiesterases as drug targets. Springer, Heidelberg
-
(2011)
Phosphodiesterases As Drug Targets
-
-
Tenor, H.1
Hatzelmann, A.2
Beume, R.3
Lahu, G.4
Zech, K.5
Bethke, T.D.6
-
156
-
-
0026444440
-
Partial mapping of cyclic nucleotide sites and studies of regulatory mechanisms of phosphodiesterases using cyclic nucleotide analogues
-
Thomas MK, Francis SH, Beebe SJ, Gettys TW, Corbin JD (1992) Partial mapping of cyclic nucleotide sites and studies of regulatory mechanisms of phosphodiesterases using cyclic nucleotide analogues. Adv Second Messenger Phosphoprotein Res 25:45-53
-
(1992)
Adv Second Messenger Phosphoprotein Res
, vol.25
, pp. 45-53
-
-
Thomas, M.K.1
Francis, S.H.2
Beebe, S.J.3
Gettys, T.W.4
Corbin, J.D.5
-
157
-
-
0025999955
-
Cyclic nucleotide phosphodiesterases: Pharmacology, biochemistry and function
-
Thompson WJ (1991) Cyclic nucleotide phosphodiesterases: pharmacology, biochemistry and function. Pharmacol Ther 51:13-33
-
(1991)
Pharmacol Ther
, vol.51
, pp. 13-33
-
-
Thompson, W.J.1
-
158
-
-
0032510819
-
Dual inhibition of human type 4 phosphodiesterase isostates by (R*,R*)-(±)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4- methoxyphenyl]-3- methyl-1-pyrrolidinecarboxylate
-
DOI 10.1021/bi972700v
-
Tian G, Rocque WJ, Wiseman JS, Thompson IZ, Holmes WD, Domanico PL, Stafford JA, Feldman PL, Luther MA (1998) Dual inhibition of human type 4 phosphodiesterase isostates by (R, R)-(+/-)-methyl 3-acetyl-4-[3- (cyclopentyloxy)-4-methoxyphenyl]-3-methyl-1-pyrrolidinecarboxylate. Biochemistry 37:6894-6904 (Pubitemid 28228126)
-
(1998)
Biochemistry
, vol.37
, Issue.19
, pp. 6894-6904
-
-
Tian, G.1
Rocque, W.J.2
Wiseman, J.S.3
Thompson, I.Z.4
Holmes, W.D.5
Domanico, P.L.6
Stafford, J.A.7
Feldman, P.L.8
Luther, M.A.9
-
159
-
-
44949156264
-
Vardenafil, but not sildenafil or tadalafil, has calcium-channel blocking activity in rabbit isolated pulmonary artery and human washed platelets
-
DOI 10.1038/bjp.2008.141, PII BJP2008141
-
Toque HA, Teixeira CE, Priviero FB, Morganti RP, Antunes E, De Nucci G (2008) Vardenafil, but not sildenafil or tadalafil, has calcium-channel blocking activity in rabbit isolated pulmonary artery and human washed platelets. Br J Pharmacol 154:787-796 (Pubitemid 351821591)
-
(2008)
British Journal of Pharmacology
, vol.154
, Issue.4
, pp. 787-796
-
-
Toque, H.A.1
Teixeira, C.E.2
Priviero, F.B.M.3
Morganti, R.P.4
Antunes, E.5
De Nucci, G.6
-
161
-
-
0036199266
-
Pharmacological profile of a novel phosphodiesterase 4 inhibitor, 4-(8-benzo[1,2,5]oxadiazol-5-yl-[1,7]naphthyridin-6-yl)-benzoic acid (NVP-ABE171), a 1,7-naphthyridine derivative, with anti-inflammatory activities
-
DOI 10.1124/jpet.301.1.241
-
Trifilieff A, Wyss D, Walker C, Mazzoni L, Hersperger R (2002) Pharmacological profile of a novel phosphodiesterase 4 inhibitor, 4-(8-benzo[1, 2, 5]oxadiazol-5-yl-[1, 7]naphthyridin-6-yl)-benzoic acid (NVP-ABE171), a 1, 7-naphthyridine derivative, with anti-inflammatory activities. J Pharmacol Exp Ther 301:241-248 (Pubitemid 34250301)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.301
, Issue.1
, pp. 241-248
-
-
Trifilieff, A.1
Wyss, D.2
Walker, C.3
Mazzoni, L.4
Hersperger, R.5
-
162
-
-
0032993016
-
Inhibition of cyclic GMP-binding cyclic GMP-specific phosphodiesterase (type 5) by sildenafil and related compounds
-
Turko IV, Ballard SA, Francis SH, Corbin JD (1999) Inhibition of cyclic GMP-binding cyclic GMP-specific phosphodiesterase (Type 5) by sildenafil and related compounds. Mol Pharmacol 56:124-130 (Pubitemid 29309820)
-
(1999)
Molecular Pharmacology
, vol.56
, Issue.1
, pp. 124-130
-
-
Turko, I.V.1
Ballard, S.A.2
Francis, S.H.3
Corbin, J.D.4
-
163
-
-
0027519350
-
Cloning and expression of a novel cyclic GMP-dependent protein kinase from mouse brain
-
Uhler MD (1993) Cloning and expression of a novel cyclic GMP-dependent protein kinase from mouse brain. J Biol Chem 268:13586-13591 (Pubitemid 23307789)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.18
, pp. 13586-13591
-
-
Uhler, M.D.1
-
164
-
-
70349085833
-
CGMP-hydrolytic activity and its inhibition by sildenafil in normal and failing human and mouse myocardium
-
Vandeput F, Krall J, Ockaili R, Salloum FN, Florio V, Corbin JD, Francis SH, Kukreja RC, Movsesian MA (2009) cGMP-hydrolytic activity and its inhibition by sildenafil in normal and failing human and mouse myocardium. J Pharmacol Exp Ther 330:884-891
-
(2009)
J Pharmacol Exp Ther
, vol.330
, pp. 884-891
-
-
Vandeput, F.1
Krall, J.2
Ockaili, R.3
Salloum, F.N.4
Florio, V.5
Corbin, J.D.6
Francis, S.H.7
Kukreja, R.C.8
Movsesian, M.A.9
-
165
-
-
69049103114
-
Discovery of a Novel Class of Phosphodiesterase 10A Inhibitors and Identification of Clinical Candidate 2-[4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3- yl)-phenoxymethyl]-quinoline (PF-2545920) for the Treatment of Schizophrenia (dagger) dagger Coordinates of the PDE10A crystal structures have been deposited in the Protein Data Bank for compound 1 (3HQW), 2 (3HQY), 3 (3HQW) and 9 (3HR1)
-
Verhoest PR, Chapin DS, Corman M, Fonseca K, Harms JF, Hou X, Marr ES, Menniti FS, Nelson F, OConnor R, Pandit J, Proulx-Lafrance C, Schmidt AW, Schmidt CJ, Suiciak JA, Liras S (2009) Discovery of a Novel Class of Phosphodiesterase 10A Inhibitors and Identification of Clinical Candidate 2-[4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline (PF-2545920) for the Treatment of Schizophrenia (dagger) dagger Coordinates of the PDE10A crystal structures have been deposited in the Protein Data Bank for compound 1 (3HQW), 2 (3HQY), 3 (3HQW) and 9 (3HR1). J Med Chem 52:5188
-
(2009)
J Med Chem
, vol.52
, pp. 5188
-
-
Verhoest, P.R.1
Chapin, D.S.2
Corman, M.3
Fonseca, K.4
Harms, J.F.5
Hou, X.6
Marr, E.S.7
Menniti, F.S.8
Nelson, F.9
Oconnor, R.10
Pandit, J.11
Proulx-Lafrance, C.12
Schmidt, A.W.13
Schmidt, C.J.14
Suiciak, J.A.15
Liras, S.16
-
166
-
-
0020645720
-
18O labeling of adenine nucleotide α-phosphoryls in platelets: Contribution by phosphodiesterase-catalyzed hydrolysis of cAMP
-
Walseth TF, Gander JE, Eide SJ, Krick TP, Goldberg ND (1983) 18O labeling of adenine nucleotide alpha-phosphoryls in platelets. Contribution by phosphodiesterase-catalyzed hydrolysis of cAMP. J Biol Chem 258:1544-1558 (Pubitemid 13101360)
-
(1983)
Journal of Biological Chemistry
, vol.258
, Issue.3
, pp. 1544-1558
-
-
Walseth, T.F.1
Gander, J.E.2
Eide, S.J.3
-
167
-
-
0031578230
-
Expression, purification, and characterization of human cAMP-specific phosphodiesterase (PDE4) subtypes A, B, C, and D
-
DOI 10.1006/bbrc.1997.6636
-
Wang P, Myers JG, Wu P, Cheewatrakoolpong B, Egan RW, Billah MM (1997) Expression, purification, and characterization of human cAMP-specific phosphodiesterase (PDE4) subtypes A, B, C, and D. Biochem Biophys Res Commun 234:320-324 (Pubitemid 27243900)
-
(1997)
Biochemical and Biophysical Research Communications
, vol.234
, Issue.2
, pp. 320-324
-
-
Wang, P.1
Myers, J.G.2
Wu, P.3
Cheewatrakoolpong, B.4
Egan, R.W.5
Billah, M.M.6
-
168
-
-
24744456706
-
Multiple elements jointly determine inhibitor selectivity of cyclic nucleotide phosphodiesterases 4 and 7
-
DOI 10.1074/jbc.M504398200
-
Wang H, Liu Y, Chen Y, Robinson H, Ke H (2005) Multiple elements jointly determine inhibitor selectivity of cyclic nucleotide phosphodiesterases 4 and 7. J Biol Chem 280:30949-30955 (Pubitemid 41291827)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.35
, pp. 30949-30955
-
-
Wang, H.1
Liu, Y.2
Chen, Y.3
Robinson, H.4
Ke, H.5
-
169
-
-
34347240412
-
Structural insight into substrate specificity of phosphodiesterase 10
-
DOI 10.1073/pnas.0700279104
-
Wang H, Liu Y, Hou J, Zheng M, Robinson H, Ke H (2007) Structural insight into substrate specificity of phosphodiesterase 10. Proc Natl Acad Sci USA 3;104:5782-5787 (Pubitemid 47175611)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.14
, pp. 5782-5787
-
-
Wang, H.1
Liu, Y.2
Hou, J.3
Zheng, M.4
Robinson, H.5
Ke, H.6
-
170
-
-
33746342145
-
Multiple conformations of phosphodiesterase-5: Implications for enzyme function and drug development
-
DOI 10.1074/jbc.M512527200
-
Wang H, Liu Y, Huai Q, Cai J, Zoraghi R, Francis SH, Corbin JD, Robinson H, Xin Z, Lin G, Ke H (2006) Multiple conformations of phosphodiesterase-5: implications for enzyme function and drug development. J Biol Chem 281:21469-21479 (Pubitemid 44115485)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.30
, pp. 21469-21479
-
-
Wang, H.1
Liu, Y.2
Huai, Q.3
Cai, J.4
Zoraghi, R.5
Francis, S.H.6
Corbin, J.D.7
Robinson, H.8
Xin, Z.9
Lin, G.10
Ke, H.11
-
171
-
-
36749000152
-
Structures of the four subfamilies of phosphodiesterases provide insight into the selectivity of their inhibitors
-
DOI 10.1042/BJ20070970
-
Wang H, Peng MS, Chen Y, Geng J, Robinson H, Houslay MD, Cai J, Ke H (2007) Structures of the four subfamilies of phosphodiesterase-4 provide insight into the selectivity of their inhibitors. Biochem J 408:193-201 (Pubitemid 350206342)
-
(2007)
Biochemical Journal
, vol.408
, Issue.2
, pp. 193-201
-
-
Wang, H.1
Peng, M.-S.2
Chen, Y.3
Geng, J.4
Robinson, H.5
Houslay, M.D.6
Cai, J.7
Ke, H.8
-
172
-
-
57049103481
-
Kinetic and structural studies of phosphodiesterase-8A and implication on the inhibitor selectivity
-
Wang H, Yan Z, Yang S, Cai J, Robinson H, Ke H (2008) Kinetic and structural studies of phosphodiesterase-8A and implication on the inhibitor selectivity. Biochemistry 47: 12760-12768
-
(2008)
Biochemistry
, vol.47
, pp. 12760-12768
-
-
Wang, H.1
Yan, Z.2
Yang, S.3
Cai, J.4
Robinson, H.5
Ke, H.6
-
173
-
-
37349101070
-
Conformational variations of both phosphodiesterase-5 and inhibitors provide the structural basis for the physiological effects of vardenafil and sildenafil
-
DOI 10.1124/mol.107.040212
-
Wang H, Ye M, Robinson H, Francis SH, Ke H (2008) Conformational variations of both phosphodiesterase-5 and inhibitors provide the structural basis for the physiological effects of vardenafil and sildenafil. Mol Pharmacol 73:104-110 (Pubitemid 350294201)
-
(2008)
Molecular Pharmacology
, vol.73
, Issue.1
, pp. 104-110
-
-
Wang, H.1
Ye, M.2
Robinson, H.3
Francis, S.H.4
Ke, H.5
-
174
-
-
35148897384
-
N-terminal domain of phosphodiesterase-11A4 (PDE11A4) decreases affinity of the catalytic site for substrates and tadalafil, and is involved in oligomerization
-
DOI 10.1021/bi7009629
-
Weeks JL 2nd, Zoraghi R, Francis SH, Corbin JD (2007) N-Terminal domain of phosphodiesterase-11A4 (PDE11A4) decreases affinity of the catalytic site for substrates and tadalafil, and is involved in oligomerization. Biochemistry 46:10353-10364 (Pubitemid 350067628)
-
(2007)
Biochemistry
, vol.46
, Issue.36
, pp. 10353-10364
-
-
Weeks II, J.L.1
Zoraghi, R.2
Francis, S.H.3
Corbin, J.D.4
-
175
-
-
0024361274
-
The cDNA of the two isoforms of bovine cGMP-dependent protein kinase
-
DOI 10.1016/0014-5793(89)81453-X
-
Wernet W, Flockerzi V, Hofmann F (1989) The cDNA of the two isoforms of bovine cGMPdependent protein kinase. FEBS Lett 251:191-196 (Pubitemid 19181868)
-
(1989)
FEBS Letters
, vol.251
, Issue.1-2
, pp. 191-196
-
-
Wernet, W.1
Flockerzi, V.2
Hofmann, F.3
-
176
-
-
51649121968
-
Compartmentation and compartment-specific regulation of PDE5 by protein kinase G allows selective cGMPmediated regulation of platelet functions
-
Wilson LS, Elbatarny HS, Crawley SW, Bennett BM, Maurice DH (2008) Compartmentation and compartment-specific regulation of PDE5 by protein kinase G allows selective cGMPmediated regulation of platelet functions. Proc Natl Acad Sci USA 105:13650-13655
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 13650-13655
-
-
Wilson, L.S.1
Elbatarny, H.S.2
Crawley, S.W.3
Bennett, B.M.4
Maurice, D.H.5
-
177
-
-
4444349218
-
Molecular determinants for cyclic nucleotide binding to the regulatory domains of phosphodiesterase 2A
-
DOI 10.1074/jbc.M404287200
-
Wu AY, Tang XB, Martinez SE, Ikeda K, Beavo JA (2004) Molecular determinants for cyclic nucleotide binding to the regulatory domains of phosphodiesterase 2A. J Biol Chem 279: 37928-37938 (Pubitemid 39195508)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.36
, pp. 37928-37938
-
-
Wu, A.Y.1
Tang, X.-B.2
Martinez, S.E.3
Ikeda, K.4
Beavo, J.A.5
-
178
-
-
0034625541
-
Atomic structure of PDE4: Insights into phosphodiesterase mechanism and specificity
-
DOI 10.1126/science.288.5472.1822
-
Xu RX, Hassell AM, Vanderwall D, Lambert MH, Holmes WD, Luther MA, Rocque WJ, Milburn MV, Zhao Y, Ke H, Nolte RT (2000) Atomic structure of PDE4: insights into phosphodiesterase mechanism and specificity. Science 288:1822-1825 (Pubitemid 30399019)
-
(2000)
Science
, vol.288
, Issue.5472
, pp. 1822-1825
-
-
Xu, R.X.1
Hassell, A.M.2
Vanderwall, D.3
Lambert, M.H.4
Holmes, W.D.5
Luther, M.A.6
Rocque, W.J.7
Milburn, M.V.8
Zhao, Y.9
Ke, H.10
Nolte, R.T.11
-
179
-
-
1442323778
-
Crystal structures of the catalytic domain of phosphodiesterase 4B complexed with amp, 8-Br-AMP, and rolipram
-
DOI 10.1016/j.jmb.2004.01.040, PII S002228360400110X
-
Xu RX, Rocque WJ, Lambert MH, Vanderwall DE, Luther MA, Nolte RT (2004) Crystal structures of the catalytic domain of phosphodiesterase 4B complexed with AMP, 8-Br-AMP, and rolipram. J Mol Biol 337:355-365 (Pubitemid 38293404)
-
(2004)
Journal of Molecular Biology
, vol.337
, Issue.2
, pp. 355-365
-
-
Xu, R.X.1
Rocque, W.J.2
Lambert, M.H.3
Vanderwall, D.E.4
Luther, M.A.5
Nolte, R.T.6
-
180
-
-
0021077241
-
Complex effects of inhibitors on cyclic GMP-stimulated cyclic nucleotide phosphodiesterase
-
Yamamoto T, Yamamoto S, Osborne JC Jr, Manganiello VC, Vaughan M, Hidaka H (1983) Complex effects of inhibitors on cyclic GMP-stimulated cyclic nucleotide phosphodiesterase. J Biol Chem 258:14173-14177 (Pubitemid 14217936)
-
(1983)
Journal of Biological Chemistry
, vol.258
, Issue.23
, pp. 14173-14177
-
-
Yamamoto, T.1
Yamamoto, S.2
Osborne Jr., J.C.3
-
181
-
-
0029845929
-
The calmodulin-dependent phosphodiesterase gene PDE1C encodes several functionally different splice variants in a tissue-specific manner
-
DOI 10.1074/jbc.271.41.25699
-
Yan C, Zhao AZ, Bentley JK, Beavo JA (1996) The calmodulin-dependent phosphodiesterase gene PDE1C encodes several functionally different splice variants in a tissue-specific manner. J Biol Chem 271:25699-25706 (Pubitemid 26337952)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.41
, pp. 25699-25706
-
-
Yan, C.1
Zhao, A.Z.2
Bentley, J.K.3
Beavo, J.A.4
-
182
-
-
0033591233
-
The RACK1 signaling scaffold protein selectively interacts with the cAMP-specific phosphodiesterase PDE4D5 isoform
-
Yarwood SJ, Steele MR, Scotland G, Houslay MD, Bolger GB (1999) The RACK1 signaling scaffold protein selectively interacts with the cAMP-specific phosphodiesterase PDE4D5 isoform. J Biol Chem 274:14909-14917
-
(1999)
J Biol Chem
, vol.274
, pp. 14909-14917
-
-
Yarwood, S.J.1
Steele, M.R.2
Scotland, G.3
Houslay, M.D.4
Bolger, G.B.5
-
183
-
-
0036500494
-
Discrete microdomains with high concentration of cAMP in stimulated rat neonatal cardiac myocytes
-
DOI 10.1126/science.1069982
-
Zaccolo M, Pozzan T (2002) Discrete microdomains with high concentration of cAMP in stimulated rat neonatal cardiac myocytes. Science 295:1711-1715 (Pubitemid 34202906)
-
(2002)
Science
, vol.295
, Issue.5560
, pp. 1711-1715
-
-
Zaccolo, M.1
Pozzan, T.2
-
184
-
-
85132515827
-
Crystal structure of phosphodiesterase families and the potential for rational drug design
-
Beavo J, Francis SH, Houslay MD (eds) CRC Press, Boca Raton
-
Zhang KYJ (2006) Crystal structure of phosphodiesterase families and the potential for rational drug design. In: Beavo J, Francis SH, Houslay MD (eds) Cyclic nucleotide phosphodiesterase in health and disease. CRC Press, Boca Raton, pp 583-605
-
(2006)
Cyclic Nucleotide Phosphodiesterase in Health and Disease
, pp. 583-605
-
-
Zhang, K.Y.J.1
-
185
-
-
0036765991
-
Identification of interaction sites of cyclic nucleotide phosphodiesterase type 3A with milrinone and cilostazol using molecular modeling and site-directed mutagenesis
-
DOI 10.1124/mol.62.3.514
-
Zhang W, Ke H, Colman RW (2002) Identification of interaction sites of cyclic nucleotide phosphodiesterase type 3A with milrinone and cilostazol using molecular modeling and sitedirected mutagenesis. Mol Pharmacol 62:514-520 (Pubitemid 36329369)
-
(2002)
Molecular Pharmacology
, vol.62
, Issue.3
, pp. 514-520
-
-
Zhang, W.1
Ke, H.2
Colman, R.W.3
-
186
-
-
27244459472
-
Efficacy and selectivity of phosphodiesterase-targeted drugs in inhibiting photoreceptor phosphodiesterase (PDE6) in retinal photoreceptors
-
DOI 10.1167/iovs.05-0257
-
Zhang X, Feng Q, Cote RH (2005) Efficacy and selectivity of phosphodiesterase-targeted drugs in inhibiting photoreceptor phosphodiesterase (PDE6) in retinal photoreceptors. Invest Ophthalmol Vis Sci 46:3060-3066 (Pubitemid 44264288)
-
(2005)
Investigative Ophthalmology and Visual Science
, vol.46
, Issue.9
, pp. 3060-3066
-
-
Zhang, X.1
Feng, Q.2
Cote, R.H.3
-
187
-
-
77951151609
-
Structural requirements of the photoreceptor phosphodiesterase {gamma}-subunit for inhibition of rod PDE6 holoenzyme and for its activation by transducin
-
Zhang XJ, Skiba NP, Cote RH (2009) Structural requirements of the photoreceptor phosphodiesterase {gamma}-subunit for inhibition of rod PDE6 holoenzyme and for its activation by transducin. J Biol Chem 285:4455-4463
-
(2009)
J Biol Chem
, vol.285
, pp. 4455-4463
-
-
Zhang, X.J.1
Skiba, N.P.2
Cote, R.H.3
-
189
-
-
33847644982
-
The novel functions of cGMP-specific phosphodiesterase 5 and its inhibitors in carcinoma cells and pulmonary/cardiovascular vessels
-
DOI 10.2174/156802607779941198
-
Zhu B, Strada SJ (2007) The novel functions of cGMP-specific phosphodiesterase 5 and its inhibitors in carcinoma cells and pulmonary/cardiovascular vessels. Curr Top Med Chem 7: 437-454 (Pubitemid 46358655)
-
(2007)
Current Topics in Medicinal Chemistry
, vol.7
, Issue.4
, pp. 437-454
-
-
Zhu, B.1
Strada, S.J.2
-
190
-
-
1642457208
-
Properties and functions of GAF domains in cyclic nucleotide phosphodiesterases and other proteins
-
DOI 10.1124/mol.65.2.267
-
Zoraghi R, Corbin JD, Francis SH (2004) Properties and functions of GAF domains in cyclic nucleotide phosphodiesterases and other proteins. Mol Pharmacol 65:267-278 (Pubitemid 38134253)
-
(2004)
Molecular Pharmacology
, vol.65
, Issue.2
, pp. 267-278
-
-
Zoraghi, R.1
Corbin, J.D.2
Francis, S.H.3
-
191
-
-
15744369740
-
Structural and functional features in human PDE5A1 regulatory domain that provide for allosteric cGMP binding, dimerization, and regulation
-
DOI 10.1074/jbc.M413611200
-
Zoraghi R, Bessay EP, Corbin JD, Francis SH (2005) Structural and functional features in human PDE5A1 regulatory domain that provide for allosteric cGMP binding, dimerization, and regulation. J Biol Chem 280:12051-12063 (Pubitemid 40418524)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.12
, pp. 12051-12063
-
-
Zoraghi, R.1
Bessay, E.P.2
Corbin, J.D.3
Francis, S.H.4
-
192
-
-
36749009575
-
Critical amino acids in phosphodiesterase-5 catalytic site that provide for high-affinity interaction with cyclic guanosine monophosphate and inhibitors
-
DOI 10.1021/bi7010702
-
Zoraghi R, Francis SH, Corbin JD (2007) Critical amino acids in phosphodiesterase-5 catalytic site that provide for high-affinity interaction with cGMP and inhibitors. Biochemistry 46: 13554-13563 (Pubitemid 350209951)
-
(2007)
Biochemistry
, vol.46
, Issue.47
, pp. 13554-13563
-
-
Zoraghi, R.1
Francis, S.H.2
Corbin, J.D.3
|