-
1
-
-
0030938936
-
G-protein-coupled receptors: molecular mechanisms involved in receptor activation and selectivity of G-protein recognition
-
Wess J. G-protein-coupled receptors: molecular mechanisms involved in receptor activation and selectivity of G-protein recognition. FASEB J 5 (1997) 346-354
-
(1997)
FASEB J
, vol.5
, pp. 346-354
-
-
Wess, J.1
-
2
-
-
0028815402
-
Cloning and pharmacological characterization of human alpha-1 adrenergic receptors: sequence corrections and direct comparison with other species homologues
-
Schwinn D.A., Johnston G.I., Page S.O., Mosley M.J., Wilson K.H., Worman N.P., et al. Cloning and pharmacological characterization of human alpha-1 adrenergic receptors: sequence corrections and direct comparison with other species homologues. J Pharmacol Exp Ther 272 (1995) 134-142
-
(1995)
J Pharmacol Exp Ther
, vol.272
, pp. 134-142
-
-
Schwinn, D.A.1
Johnston, G.I.2
Page, S.O.3
Mosley, M.J.4
Wilson, K.H.5
Worman, N.P.6
-
3
-
-
0030577241
-
Amino acids of the alpha1B-adrenergic receptor involved in agonist binding: differences in docking catecholamines to receptor subtypes
-
Cavalli A., Fanelli F., Taddei C., De Benedetti P.G., and Cotecchia S. Amino acids of the alpha1B-adrenergic receptor involved in agonist binding: differences in docking catecholamines to receptor subtypes. FEBS Lett 399 (1996) 9-13
-
(1996)
FEBS Lett
, vol.399
, pp. 9-13
-
-
Cavalli, A.1
Fanelli, F.2
Taddei, C.3
De Benedetti, P.G.4
Cotecchia, S.5
-
4
-
-
0029866748
-
Identification of critical determinants of alpha1-adrenergic receptor subtype selective agonist binding
-
Hwa J., and Perez D.M. Identification of critical determinants of alpha1-adrenergic receptor subtype selective agonist binding. J Biol Chem 271 (1996) 6322-6327
-
(1996)
J Biol Chem
, vol.271
, pp. 6322-6327
-
-
Hwa, J.1
Perez, D.M.2
-
5
-
-
77957055780
-
Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G-protein coupled receptors
-
Ballesteros J.A., and Weinstein H. Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G-protein coupled receptors. Meth Neurosci 25 (1995) 366-428
-
(1995)
Meth Neurosci
, vol.25
, pp. 366-428
-
-
Ballesteros, J.A.1
Weinstein, H.2
-
6
-
-
0033522643
-
Phe310 in transmembrane VI of the alpha1B-adrenergic receptor is a key switch residue involved in activation and catecholamine ring aromatic bonding
-
Chen S., Xu M., Lin F., Lee D., Riek P., and Graham R.M. Phe310 in transmembrane VI of the alpha1B-adrenergic receptor is a key switch residue involved in activation and catecholamine ring aromatic bonding. J Biol Chem 274 (1999) 16320-16330
-
(1999)
J Biol Chem
, vol.274
, pp. 16320-16330
-
-
Chen, S.1
Xu, M.2
Lin, F.3
Lee, D.4
Riek, P.5
Graham, R.M.6
-
7
-
-
0032740152
-
Theoretical study on the electrostatically driven step of receptor-G protein recognition
-
Fanelli F., Menziani C., Scheer A., Cotecchia S., and De Benedetti P.G. Theoretical study on the electrostatically driven step of receptor-G protein recognition. Proteins: Struct Funct Genet 37 (1999) 145-156
-
(1999)
Proteins: Struct Funct Genet
, vol.37
, pp. 145-156
-
-
Fanelli, F.1
Menziani, C.2
Scheer, A.3
Cotecchia, S.4
De Benedetti, P.G.5
-
8
-
-
0035824582
-
Mutational and computational analysis of the alpha1b-adrenergic receptor: involvement of basic and hydrophobic residues in receptor activation and G protein coupling
-
Greasley P.J., Fanelli F., Scheer A., Abuin L., Nenniger-Tosato M., De Benedetti P.G., et al. Mutational and computational analysis of the alpha1b-adrenergic receptor: involvement of basic and hydrophobic residues in receptor activation and G protein coupling. J Biol Chem 276 (2001) 46485-46494
-
(2001)
J Biol Chem
, vol.276
, pp. 46485-46494
-
-
Greasley, P.J.1
Fanelli, F.2
Scheer, A.3
Abuin, L.4
Nenniger-Tosato, M.5
De Benedetti, P.G.6
-
9
-
-
0028059202
-
Truncation of the receptor impairs agonist-induced phosphorylation and desensitization of the alpha1B-adrenergic receptor
-
Lattion A.L., Diviani D., and Cotecchia S. Truncation of the receptor impairs agonist-induced phosphorylation and desensitization of the alpha1B-adrenergic receptor. J Biol Chem 269 (1994) 22887-22893
-
(1994)
J Biol Chem
, vol.269
, pp. 22887-22893
-
-
Lattion, A.L.1
Diviani, D.2
Cotecchia, S.3
-
10
-
-
0029976109
-
Effect of different G protein-coupled receptor kinase- and protein kinase C-mediated desensitization of the alpha1B-adrenergic receptor
-
Diviani D., Lattion A.L., Larbi N., Kunapuli P., Pronin A., Benovic J.L., et al. Effect of different G protein-coupled receptor kinase- and protein kinase C-mediated desensitization of the alpha1B-adrenergic receptor. J Biol Chem 271 (1996) 5049-5058
-
(1996)
J Biol Chem
, vol.271
, pp. 5049-5058
-
-
Diviani, D.1
Lattion, A.L.2
Larbi, N.3
Kunapuli, P.4
Pronin, A.5
Benovic, J.L.6
-
11
-
-
0030699386
-
Characterization of the phosphorylation sites involved in G protein-coupled receptor kinase and protein kinase C-mediated desensitization of the alpha1B-adrenergic receptor
-
Diviani D., Lattion A.L., and Cotecchia S. Characterization of the phosphorylation sites involved in G protein-coupled receptor kinase and protein kinase C-mediated desensitization of the alpha1B-adrenergic receptor. J Biol Chem 272 (1997) 28712-28719
-
(1997)
J Biol Chem
, vol.272
, pp. 28712-28719
-
-
Diviani, D.1
Lattion, A.L.2
Cotecchia, S.3
-
12
-
-
0025212680
-
Regions of alpha1-adrenergic receptor involved in coupling to phosphatidylinositol hydrolysis and enhanced sensivity of biological function
-
Cotecchia S., Exum S., Caron M.G., and Lefkowitz R.J. Regions of alpha1-adrenergic receptor involved in coupling to phosphatidylinositol hydrolysis and enhanced sensivity of biological function. Proc Natl Acad Sci USA 87 (1990) 2896-2900
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 2896-2900
-
-
Cotecchia, S.1
Exum, S.2
Caron, M.G.3
Lefkowitz, R.J.4
-
13
-
-
0026592357
-
Constitutive activation of the alpha1B-adrenergic receptor by all amino acid substitution at a single site
-
Kjelsberg M.A., Cotecchia S., Ostrowski J., Caron M.G., and Lefkowitz R.J. Constitutive activation of the alpha1B-adrenergic receptor by all amino acid substitution at a single site. J Biol Chem 267 (1992) 1430-1433
-
(1992)
J Biol Chem
, vol.267
, pp. 1430-1433
-
-
Kjelsberg, M.A.1
Cotecchia, S.2
Ostrowski, J.3
Caron, M.G.4
Lefkowitz, R.J.5
-
16
-
-
0029093559
-
G protein-coupled receptor structure and function: the impact of disease-causing mutations
-
Shenker A.G. G protein-coupled receptor structure and function: the impact of disease-causing mutations. Baillières Clin Endocrin Metabol 9 (1995) 427-451
-
(1995)
Baillières Clin Endocrin Metabol
, vol.9
, pp. 427-451
-
-
Shenker, A.G.1
-
17
-
-
0030614337
-
The activation process of the alpha1B-adrenergic receptor: potential role of protonation and hydrophobicity of a highly conserved aspartate
-
Scheer A., Fanelli F., Costa T., De Benedetti P.G., and Cotecchia S. The activation process of the alpha1B-adrenergic receptor: potential role of protonation and hydrophobicity of a highly conserved aspartate. Proc Natl Acad Sci USA 94 (1997) 808-813
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 808-813
-
-
Scheer, A.1
Fanelli, F.2
Costa, T.3
De Benedetti, P.G.4
Cotecchia, S.5
-
18
-
-
0027298812
-
Constitutive activation of opsin: influence of charge at position 134 and size at position 296
-
Cohen G.B., Yang T., Robinson P.R., and Oprian D.D. Constitutive activation of opsin: influence of charge at position 134 and size at position 296. Biochemistry 32 (1993) 6111-6115
-
(1993)
Biochemistry
, vol.32
, pp. 6111-6115
-
-
Cohen, G.B.1
Yang, T.2
Robinson, P.R.3
Oprian, D.D.4
-
19
-
-
0033061256
-
Mutation of highly conserved aspartic acid in the beta2 adrenergic receptor: constitutive activation, structural instability and conformational rearrangement of transmembrane segment 6
-
Rasmussen S.G.F., Jensen A.D., Liapakis G., Ghanouni P., Javitch J.A., and Gether U. Mutation of highly conserved aspartic acid in the beta2 adrenergic receptor: constitutive activation, structural instability and conformational rearrangement of transmembrane segment 6. Mol Pharmacol 56 (1999) 175-184
-
(1999)
Mol Pharmacol
, vol.56
, pp. 175-184
-
-
Rasmussen, S.G.F.1
Jensen, A.D.2
Liapakis, G.3
Ghanouni, P.4
Javitch, J.A.5
Gether, U.6
-
20
-
-
0034112037
-
The effect of mutations in the DRY motif on the constitutive activity and structural instability of the histamine H(2) receptor
-
Alewijnse A.E., Timmerman H., Jacobs E.H., Smit M.J., Roovers E., Cotecchia S., et al. The effect of mutations in the DRY motif on the constitutive activity and structural instability of the histamine H(2) receptor. Mol Pharmacol 57 (2000) 890-898
-
(2000)
Mol Pharmacol
, vol.57
, pp. 890-898
-
-
Alewijnse, A.E.1
Timmerman, H.2
Jacobs, E.H.3
Smit, M.J.4
Roovers, E.5
Cotecchia, S.6
-
21
-
-
0032217226
-
The D136A mutation of the V2 vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities
-
Morin D., Cotte N., Balestre M.N., Mouillac B., Manning M., Breton C., et al. The D136A mutation of the V2 vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities. FEBS Lett 441 (1998) 470-475
-
(1998)
FEBS Lett
, vol.441
, pp. 470-475
-
-
Morin, D.1
Cotte, N.2
Balestre, M.N.3
Mouillac, B.4
Manning, M.5
Breton, C.6
-
22
-
-
0031037632
-
The role of the aspartate-arginine-tyrosine triad in the m1 muscarinic receptor: mutations of aspartate 122 and tyrosine 124 decrease receptor expression but do not abolish signaling
-
Lu Z.L., Curtis C.A., Jones P.G., Pavia J., and Hulme E.C. The role of the aspartate-arginine-tyrosine triad in the m1 muscarinic receptor: mutations of aspartate 122 and tyrosine 124 decrease receptor expression but do not abolish signaling. Mol Pharmacol 51 (1997) 234-241
-
(1997)
Mol Pharmacol
, vol.51
, pp. 234-241
-
-
Lu, Z.L.1
Curtis, C.A.2
Jones, P.G.3
Pavia, J.4
Hulme, E.C.5
-
23
-
-
0033974265
-
Mutational analysis of the highly conserved arginine within the Glu/Asp-Arg-Tyr motif of the alpha(1b)-adrenergic receptor: effects on receptor isomerization and activation
-
Scheer A., Costa T., Fanelli F., De Benedetti P.G., Mhaouty-Kodja S., Abuin L., et al. Mutational analysis of the highly conserved arginine within the Glu/Asp-Arg-Tyr motif of the alpha(1b)-adrenergic receptor: effects on receptor isomerization and activation. Mol Pharmacol 57 (2000) 219-231
-
(2000)
Mol Pharmacol
, vol.57
, pp. 219-231
-
-
Scheer, A.1
Costa, T.2
Fanelli, F.3
De Benedetti, P.G.4
Mhaouty-Kodja, S.5
Abuin, L.6
-
24
-
-
0033520912
-
Characteristics for a salt-bridge switch mutation of the alpha(1b) adrenergic receptor. Altered pharmacology and rescue of constitutive activity
-
Porter J.E., and Perez D.M. Characteristics for a salt-bridge switch mutation of the alpha(1b) adrenergic receptor. Altered pharmacology and rescue of constitutive activity. J Biol Chem 274 (1999) 34535-34538
-
(1999)
J Biol Chem
, vol.274
, pp. 34535-34538
-
-
Porter, J.E.1
Perez, D.M.2
-
25
-
-
0029664397
-
Chimeras of alpha1-adrenergic receptor subtypes identify critical residues that modulate active state isomerization
-
Hwa J., Graham R.M., and Perez D.M. Chimeras of alpha1-adrenergic receptor subtypes identify critical residues that modulate active state isomerization. J Biol Chem 271 14 (1996) 7956-7964
-
(1996)
J Biol Chem
, vol.271
, Issue.14
, pp. 7956-7964
-
-
Hwa, J.1
Graham, R.M.2
Perez, D.M.3
-
26
-
-
0036239236
-
Mutagenesis and modelling of the alpha1b-adrenergic receptor highlights the role of the helix3/helix 6 interface in receptor activation
-
Greasley P., Fanelli F., Rossier O., Abuin L., and Cotecchia S. Mutagenesis and modelling of the alpha1b-adrenergic receptor highlights the role of the helix3/helix 6 interface in receptor activation. Mol Pharmacol 61 (2002) 1025-1032
-
(2002)
Mol Pharmacol
, vol.61
, pp. 1025-1032
-
-
Greasley, P.1
Fanelli, F.2
Rossier, O.3
Abuin, L.4
Cotecchia, S.5
-
27
-
-
0034604451
-
Crystal structure of rhodopsin: a G protein-coupled receptor
-
Palczewski C., Kumasaka T., Hori T., Behnke C.A., Motoshima H., Fox B.A., et al. Crystal structure of rhodopsin: a G protein-coupled receptor. Science 289 (2000) 739-745
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, C.1
Kumasaka, T.2
Hori, T.3
Behnke, C.A.4
Motoshima, H.5
Fox, B.A.6
-
28
-
-
0032749712
-
Inverse agonism and neutral antagonism at alpha(1a)- and alpha(1b)-adrenergic receptor subtypes
-
Rossier O., Abuin L., Fanelli F., Leonardi A., and Cotecchia S. Inverse agonism and neutral antagonism at alpha(1a)- and alpha(1b)-adrenergic receptor subtypes. Mol Pharmacol 56 (1999) 858-866
-
(1999)
Mol Pharmacol
, vol.56
, pp. 858-866
-
-
Rossier, O.1
Abuin, L.2
Fanelli, F.3
Leonardi, A.4
Cotecchia, S.5
-
29
-
-
0035800032
-
Advances in determination of a high-resolution three-dimensional structure of rhodopsin, a model of G-protein-coupled receptors (GPCRs)
-
Teller D.C., Okada T., Behnke C.A., and Palczewski C. Advances in determination of a high-resolution three-dimensional structure of rhodopsin, a model of G-protein-coupled receptors (GPCRs). Biochemistry 40 (2001) 7761-7772
-
(2001)
Biochemistry
, vol.40
, pp. 7761-7772
-
-
Teller, D.C.1
Okada, T.2
Behnke, C.A.3
Palczewski, C.4
-
30
-
-
0037197848
-
Functional role of internal water molecules in rhodopsin revealed by X-ray crystallography
-
Okada T., Fujiyoshi Y., Silow M., Navarro J., Landau E.M., and Shichida Y. Functional role of internal water molecules in rhodopsin revealed by X-ray crystallography. Proc Natl Acad Sci USA 99 (2002) 5982-5987
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 5982-5987
-
-
Okada, T.1
Fujiyoshi, Y.2
Silow, M.3
Navarro, J.4
Landau, E.M.5
Shichida, Y.6
-
31
-
-
0034464742
-
Uncovering molecular mechanisms involved in activation of G protein-coupled receptors
-
Gether U. Uncovering molecular mechanisms involved in activation of G protein-coupled receptors. Endocr Rev 21 (2000) 90-113
-
(2000)
Endocr Rev
, vol.21
, pp. 90-113
-
-
Gether, U.1
-
32
-
-
0036783213
-
Lessons from constitutively active mutants of G protein-coupled receptors
-
Parnot C., Miserey-Lenkei S., Bardin S., Corvol P., and Clauser E. Lessons from constitutively active mutants of G protein-coupled receptors. Trends Endocrinol Metabol 13 (2002) 336-343
-
(2002)
Trends Endocrinol Metabol
, vol.13
, pp. 336-343
-
-
Parnot, C.1
Miserey-Lenkei, S.2
Bardin, S.3
Corvol, P.4
Clauser, E.5
-
33
-
-
0034016295
-
Inverse agonism at G protein coupled receptors: (patho)physiological relevance and implications for drug discovery
-
de Ligt R.A.F., Kourounakis A.P., and IJzerman A.P. Inverse agonism at G protein coupled receptors: (patho)physiological relevance and implications for drug discovery. Br J Pharmacol 130 (2000) 1-12
-
(2000)
Br J Pharmacol
, vol.130
, pp. 1-12
-
-
de Ligt, R.A.F.1
Kourounakis, A.P.2
IJzerman, A.P.3
-
34
-
-
0347627709
-
Constitutively activity and inverse agonists of G protein-coupled receptors: a current perspective
-
Milligan G. Constitutively activity and inverse agonists of G protein-coupled receptors: a current perspective. Mol Pharmacol 64 (2003) 1271-1276
-
(2003)
Mol Pharmacol
, vol.64
, pp. 1271-1276
-
-
Milligan, G.1
-
35
-
-
0029829504
-
Coupling efficiencies of human alpha 1-adrenergic receptor subtypes: titration of receptor density and responsiveness with inducible and repressible expression vectors
-
Theroux T.L., Esbenshade T.A., Peavy R.D., and Minneman K.P. Coupling efficiencies of human alpha 1-adrenergic receptor subtypes: titration of receptor density and responsiveness with inducible and repressible expression vectors. Mol Pharmacol 50 (1996) 1376-1387
-
(1996)
Mol Pharmacol
, vol.50
, pp. 1376-1387
-
-
Theroux, T.L.1
Esbenshade, T.A.2
Peavy, R.D.3
Minneman, K.P.4
-
36
-
-
0032999420
-
Modulation of basal intracellular calcium by inverse agonists and phorbol myristate acetate in rat-1 fibroblasts stably expressing alpha 1d-adrenoceptors
-
Garcia-Sainz J.A., and Torres-Padilla M.E. Modulation of basal intracellular calcium by inverse agonists and phorbol myristate acetate in rat-1 fibroblasts stably expressing alpha 1d-adrenoceptors. FEBS Lett (1999) 277-281
-
(1999)
FEBS Lett
, pp. 277-281
-
-
Garcia-Sainz, J.A.1
Torres-Padilla, M.E.2
-
37
-
-
0034034073
-
Regulation of the cellular localization and signaling properties of the alpha1B-and alpha1D-Adrenoceptors by agonists and inverse agonists
-
McCune D.F., Edelmann S.E., Olges J.R., Ginell R.P., Waldrop B.A., Waugh D.J.J., et al. Regulation of the cellular localization and signaling properties of the alpha1B-and alpha1D-Adrenoceptors by agonists and inverse agonists. Mol Pharmacol 57 (2000) 659-666
-
(2000)
Mol Pharmacol
, vol.57
, pp. 659-666
-
-
McCune, D.F.1
Edelmann, S.E.2
Olges, J.R.3
Ginell, R.P.4
Waldrop, B.A.5
Waugh, D.J.J.6
-
38
-
-
0036157202
-
Pathological role of constitutively active population of alpha1D-Adrenoceptors in arteries of spontaneously hypertensive rats
-
Gisbert R., Ziani K., Miquel R., Noguera A., Ivorra M.D., Anselmi E., et al. Pathological role of constitutively active population of alpha1D-Adrenoceptors in arteries of spontaneously hypertensive rats. Br J Pharmacol 135 (2002) 206-216
-
(2002)
Br J Pharmacol
, vol.135
, pp. 206-216
-
-
Gisbert, R.1
Ziani, K.2
Miquel, R.3
Noguera, A.4
Ivorra, M.D.5
Anselmi, E.6
-
39
-
-
27744451411
-
Historical review: negative efficacy and the constitutive activity of G-protein coupled receptors
-
Costa T., and Cotecchia S. Historical review: negative efficacy and the constitutive activity of G-protein coupled receptors. Trends Pharmacol Sci 26 (2005) 618-624
-
(2005)
Trends Pharmacol Sci
, vol.26
, pp. 618-624
-
-
Costa, T.1
Cotecchia, S.2
-
40
-
-
0030752182
-
Up-regulation of the levels of expression and function of a constitutively active mutant of the hamster alpha1B-adrenoceptor by ligands that act as inverse agonists
-
Lee T.W., Cotecchia S., and Milligan G. Up-regulation of the levels of expression and function of a constitutively active mutant of the hamster alpha1B-adrenoceptor by ligands that act as inverse agonists. Biochem J 325 (1997) 733-739
-
(1997)
Biochem J
, vol.325
, pp. 733-739
-
-
Lee, T.W.1
Cotecchia, S.2
Milligan, G.3
|