-
1
-
-
66949176303
-
Venomics as a drug discovery platform
-
Escoubas P, King GF, (2009) Venomics as a drug discovery platform. Expert Rev Proteomics 6: 221-224.
-
(2009)
Expert Rev Proteomics
, vol.6
, pp. 221-224
-
-
Escoubas, P.1
King, G.F.2
-
2
-
-
67649592405
-
Conotoxins: natural product drug leads
-
Halai R, Craik DJ, (2009) Conotoxins: natural product drug leads. Nat Prod Rep 26: 526-536.
-
(2009)
Nat Prod Rep
, vol.26
, pp. 526-536
-
-
Halai, R.1
Craik, D.J.2
-
3
-
-
0242331757
-
Therapeutic potential of venom peptides
-
Lewis RJ, Garcia ML, (2003) Therapeutic potential of venom peptides. Nat Rev Drug Discov 2: 790-802.
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 790-802
-
-
Lewis, R.J.1
Garcia, M.L.2
-
4
-
-
0033997841
-
Conopeptides: From deadly venoms to novel therapeutics
-
Shen GS, Layer RT, McCabe RT, (2000) Conopeptides: From deadly venoms to novel therapeutics. Drug Discov Today 5: 98-106.
-
(2000)
Drug Discov Today
, vol.5
, pp. 98-106
-
-
Shen, G.S.1
Layer, R.T.2
McCabe, R.T.3
-
5
-
-
84857040368
-
G protein-coupled receptors, an unexploited animal toxin targets: Exploration of green mamba venom for novel drug candidates active against adrenoceptors
-
Maïga A, Mourier G, Quinton L, Rouget C, Gales C, et al. (2012) G protein-coupled receptors, an unexploited animal toxin targets: Exploration of green mamba venom for novel drug candidates active against adrenoceptors. Toxicon 59: 487-496.
-
(2012)
Toxicon
, vol.59
, pp. 487-496
-
-
Maïga, A.1
Mourier, G.2
Quinton, L.3
Rouget, C.4
Gales, C.5
-
6
-
-
65549088983
-
Muscarinic toxins: tools for the study of the pharmacological and functional properties of muscarinic receptors
-
Servent D, Fruchart-Gaillard C, (2009) Muscarinic toxins: tools for the study of the pharmacological and functional properties of muscarinic receptors. J Neurochem 109: 1193-1202.
-
(2009)
J Neurochem
, vol.109
, pp. 1193-1202
-
-
Servent, D.1
Fruchart-Gaillard, C.2
-
7
-
-
0141817957
-
Allosteric alpha 1-adrenoreceptor antagonism by the conopeptide rho-TIA
-
Sharpe IA, Thomas L, Loughnan M, Motin L, Palant E, et al. (2003) Allosteric alpha 1-adrenoreceptor antagonism by the conopeptide rho-TIA. J Biol Chem 278: 34451-34457.
-
(2003)
J Biol Chem
, vol.278
, pp. 34451-34457
-
-
Sharpe, I.A.1
Thomas, L.2
Loughnan, M.3
Motin, L.4
Palant, E.5
-
8
-
-
35948930215
-
Beta-cardiotoxin: a new three-finger toxin from Ophiophagus hannah (king cobra) venom with beta-blocker activity
-
Rajagopalan N, Pung YF, Zhu YZ, Wong PT, Kumar PP, et al. (2007) Beta-cardiotoxin: a new three-finger toxin from Ophiophagus hannah (king cobra) venom with beta-blocker activity. Faseb J 21: 3685-3695.
-
(2007)
Faseb J
, vol.21
, pp. 3685-3695
-
-
Rajagopalan, N.1
Pung, Y.F.2
Zhu, Y.Z.3
Wong, P.T.4
Kumar, P.P.5
-
9
-
-
75649102086
-
Isolation and pharmacological characterization of AdTx1, a natural peptide displaying specific insurmountable antagonism of the alpha(1A)-adrenoceptor
-
Quinton L, Girard E, Maiga A, Rekik M, Lluel P, et al. (2010) Isolation and pharmacological characterization of AdTx1, a natural peptide displaying specific insurmountable antagonism of the alpha(1A)-adrenoceptor. Br J Pharmacol 159: 316-325.
-
(2010)
Br J Pharmacol
, vol.159
, pp. 316-325
-
-
Quinton, L.1
Girard, E.2
Maiga, A.3
Rekik, M.4
Lluel, P.5
-
10
-
-
78049397452
-
Identification of a novel snake peptide toxin displaying high affinity and antagonist behaviour for the alpha2-adrenoceptors
-
Rouget C, Quinton L, Maiga A, Gales C, Masuyer G, et al. (2010) Identification of a novel snake peptide toxin displaying high affinity and antagonist behaviour for the alpha2-adrenoceptors. Br J Pharmacol 161: 1361-1374.
-
(2010)
Br J Pharmacol
, vol.161
, pp. 1361-1374
-
-
Rouget, C.1
Quinton, L.2
Maiga, A.3
Gales, C.4
Masuyer, G.5
-
11
-
-
33645835941
-
Identification of various allosteric interaction sites on M1 muscarinic receptor using 125I-Met35-oxidized muscarinic toxin 7
-
Fruchart-Gaillard C, Mourier G, Marquer C, Menez A, Servent D, (2006) Identification of various allosteric interaction sites on M1 muscarinic receptor using 125I-Met35-oxidized muscarinic toxin 7. Mol Pharmacol 69: 1641-1651.
-
(2006)
Mol Pharmacol
, vol.69
, pp. 1641-1651
-
-
Fruchart-Gaillard, C.1
Mourier, G.2
Marquer, C.3
Menez, A.4
Servent, D.5
-
12
-
-
57349143427
-
Different interactions between MT7 toxin and the human muscarinic M1 receptor in its free and N-methylscopolamine-occupied states
-
Fruchart-Gaillard C, Mourier G, Marquer C, Stura E, Birdsall NJ, et al. (2008) Different interactions between MT7 toxin and the human muscarinic M1 receptor in its free and N-methylscopolamine-occupied states. Mol Pharmacol 74: 1554-1563.
-
(2008)
Mol Pharmacol
, vol.74
, pp. 1554-1563
-
-
Fruchart-Gaillard, C.1
Mourier, G.2
Marquer, C.3
Stura, E.4
Birdsall, N.J.5
-
13
-
-
80052415753
-
Structural Model of Ligand-G Protein-coupled Receptor (GPCR) Complex Based on Experimental Double Mutant Cycle Data: MT7 SNAKE TOXIN BOUND TO DIMERIC hM1 MUSCARINIC RECEPTOR
-
Marquer C, Fruchart-Gaillard C, Letellier G, Marcon E, Mourier G, et al. (2011) Structural Model of Ligand-G Protein-coupled Receptor (GPCR) Complex Based on Experimental Double Mutant Cycle Data: MT7 SNAKE TOXIN BOUND TO DIMERIC hM1 MUSCARINIC RECEPTOR. Journal of Biological Chemistry 286: 31661-31675.
-
(2011)
Journal of Biological Chemistry
, vol.286
, pp. 31661-31675
-
-
Marquer, C.1
Fruchart-Gaillard, C.2
Letellier, G.3
Marcon, E.4
Mourier, G.5
-
14
-
-
0037218331
-
Chemical synthesis of MT1 and MT7 muscarinic toxins: critical role of Arg-34 in their interaction with M1 muscarinic receptor
-
Mourier G, Dutertre S, Fruchart-Gaillard C, Menez A, Servent D, (2003) Chemical synthesis of MT1 and MT7 muscarinic toxins: critical role of Arg-34 in their interaction with M1 muscarinic receptor. Mol Pharmacol 63: 26-35.
-
(2003)
Mol Pharmacol
, vol.63
, pp. 26-35
-
-
Mourier, G.1
Dutertre, S.2
Fruchart-Gaillard, C.3
Menez, A.4
Servent, D.5
-
15
-
-
0029951802
-
Binding of the labelled muscarinic toxin 125I-MT1 to rat brain muscarinic M1 receptors
-
Waelbroeck M, De Neef P, Domenach V, Vandermeers-Piret MC, Vandermeers A, (1996) Binding of the labelled muscarinic toxin 125I-MT1 to rat brain muscarinic M1 receptors. Eur J Pharmacol 305: 187-192.
-
(1996)
Eur J Pharmacol
, vol.305
, pp. 187-192
-
-
Waelbroeck, M.1
De Neef, P.2
Domenach, V.3
Vandermeers-Piret, M.C.4
Vandermeers, A.5
-
16
-
-
1642408678
-
Action of the muscarinic toxin MT7 on agonist-bound muscarinic M1 receptors
-
Olianas MC, Adem A, Karlsson E, Onali P, (2004) Action of the muscarinic toxin MT7 on agonist-bound muscarinic M1 receptors. European Journal of Pharmacology 487: 65-72.
-
(2004)
European Journal of Pharmacology
, vol.487
, pp. 65-72
-
-
Olianas, M.C.1
Adem, A.2
Karlsson, E.3
Onali, P.4
-
17
-
-
10944228153
-
Muscarinic Toxin 7 Selectivity Is Dictated by Extracellular Receptor Loops
-
Kukkonen A, (2004) Muscarinic Toxin 7 Selectivity Is Dictated by Extracellular Receptor Loops. Journal of Biological Chemistry 279: 50923-50929.
-
(2004)
Journal of Biological Chemistry
, vol.279
, pp. 50923-50929
-
-
Kukkonen, A.1
-
18
-
-
84872689496
-
Conopeptide rho-TIA Defines a New Allosteric Site on the Extracellular Surface of the alpha1B-Adrenoceptor
-
Ragnarsson L, Wang CI, Andersson A, Fajarningsih D, Monks T, et al. (2013) Conopeptide rho-TIA Defines a New Allosteric Site on the Extracellular Surface of the alpha1B-Adrenoceptor. J Biol Chem 288: 1814-1827.
-
(2013)
J Biol Chem
, vol.288
, pp. 1814-1827
-
-
Ragnarsson, L.1
Wang, C.I.2
Andersson, A.3
Fajarningsih, D.4
Monks, T.5
-
19
-
-
12844282068
-
Differential antagonism by conotoxin rho-TIA of contractions mediated by distinct alpha1-adrenoceptor subtypes in rat vas deferens, spleen and aorta
-
Lima V, Mueller A, Kamikihara SY, Raymundi V, Alewood D, et al. (2005) Differential antagonism by conotoxin rho-TIA of contractions mediated by distinct alpha1-adrenoceptor subtypes in rat vas deferens, spleen and aorta. Eur J Pharmacol 508: 183-192.
-
(2005)
Eur J Pharmacol
, vol.508
, pp. 183-192
-
-
Lima, V.1
Mueller, A.2
Kamikihara, S.Y.3
Raymundi, V.4
Alewood, D.5
-
20
-
-
78751538699
-
Quantification of functional selectivity at the human alpha(1A)-adrenoceptor
-
Evans BA, Broxton N, Merlin J, Sato M, Hutchinson DS, et al. (2011) Quantification of functional selectivity at the human alpha(1A)-adrenoceptor. Mol Pharmacol 79: 298-307.
-
(2011)
Mol Pharmacol
, vol.79
, pp. 298-307
-
-
Evans, B.A.1
Broxton, N.2
Merlin, J.3
Sato, M.4
Hutchinson, D.S.5
-
21
-
-
0015861774
-
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
Cheng Y, Prusoff WH, (1973) Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 22: 3099-3108.
-
(1973)
Biochem Pharmacol
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
22
-
-
0032732550
-
The assessment of antagonist potency under conditions of transient response kinetics
-
Christopoulos A, Parsons AM, Lew MJ, El-Fakahany EE, (1999) The assessment of antagonist potency under conditions of transient response kinetics. Eur J Pharmacol 382: 217-227.
-
(1999)
Eur J Pharmacol
, vol.382
, pp. 217-227
-
-
Christopoulos, A.1
Parsons, A.M.2
Lew, M.J.3
El-Fakahany, E.E.4
-
23
-
-
0029094516
-
Analysis of competitive agonist-antagonist interactions by nonlinear regression
-
Lew MJ, Angus JA, (1995) Analysis of competitive agonist-antagonist interactions by nonlinear regression. Trends Pharmacol Sci 16: 328-337.
-
(1995)
Trends Pharmacol Sci
, vol.16
, pp. 328-337
-
-
Lew, M.J.1
Angus, J.A.2
-
24
-
-
0030856636
-
An improved method for analysis of competitive agonist/antagonist interactions by non-linear regression
-
Lew MJ, Angus JA, (1997) An improved method for analysis of competitive agonist/antagonist interactions by non-linear regression. Ann N Y Acad Sci 812: 179-181.
-
(1997)
Ann N Y Acad Sci
, vol.812
, pp. 179-181
-
-
Lew, M.J.1
Angus, J.A.2
-
25
-
-
0027136282
-
Comparative protein modelling by satisfaction of spatial restraints
-
Sali A, Blundell TL, (1993) Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol 234: 779-815.
-
(1993)
J Mol Biol
, vol.234
, pp. 779-815
-
-
Sali, A.1
Blundell, T.L.2
-
26
-
-
0037252680
-
GPCRDB information system for G protein-coupled receptors
-
Horn F, Bettler E, Oliveira L, Campagne F, Cohen FE, et al. (2003) GPCRDB information system for G protein-coupled receptors. Nucleic Acids Res 31: 294-297.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 294-297
-
-
Horn, F.1
Bettler, E.2
Oliveira, L.3
Campagne, F.4
Cohen, F.E.5
-
27
-
-
78651297517
-
GPCRDB: information system for G protein-coupled receptors
-
Vroling B, Sanders M, Baakman C, Borrmann A, Verhoeven S, et al. (2011) GPCRDB: information system for G protein-coupled receptors. Nucleic Acids Res 39: D309-319.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Vroling, B.1
Sanders, M.2
Baakman, C.3
Borrmann, A.4
Verhoeven, S.5
-
28
-
-
36448995359
-
High-Resolution Crystal Structure of an Engineered Human {beta}2-Adrenergic G Protein Coupled Receptor
-
Cherezov V, Rosenbaum DM, Hanson MA, Rasmussen SG, Thian FS, et al. (2007) High-Resolution Crystal Structure of an Engineered Human {beta}2-Adrenergic G Protein Coupled Receptor. Science 318: 1258-1265.
-
(2007)
Science
, vol.318
, pp. 1258-1265
-
-
Cherezov, V.1
Rosenbaum, D.M.2
Hanson, M.A.3
Rasmussen, S.G.4
Thian, F.S.5
-
29
-
-
49449116956
-
A rational nomenclature for naming peptide toxins from spiders and other venomous animals
-
King GF, Gentz MC, Escoubas P, Nicholson GM, (2008) A rational nomenclature for naming peptide toxins from spiders and other venomous animals. Toxicon 52: 264-276.
-
(2008)
Toxicon
, vol.52
, pp. 264-276
-
-
King, G.F.1
Gentz, M.C.2
Escoubas, P.3
Nicholson, G.M.4
-
30
-
-
1342323325
-
Application of a Kinetic Model to the Apparently Complex Behavior of Negative and Positive Allosteric Modulators of Muscarinic Acetylcholine Receptors
-
Avlani V, (2003) Application of a Kinetic Model to the Apparently Complex Behavior of Negative and Positive Allosteric Modulators of Muscarinic Acetylcholine Receptors. Journal of Pharmacology and Experimental Therapeutics 308: 1062-1072.
-
(2003)
Journal of Pharmacology and Experimental Therapeutics
, vol.308
, pp. 1062-1072
-
-
Avlani, V.1
-
31
-
-
0041912480
-
Structure/activity relationships of M2 muscarinic allosteric modulators
-
Mohr K, Trankle C, Holzgrabe U, (2003) Structure/activity relationships of M2 muscarinic allosteric modulators. Receptors Channels 9: 229-240.
-
(2003)
Receptors Channels
, vol.9
, pp. 229-240
-
-
Mohr, K.1
Trankle, C.2
Holzgrabe, U.3
-
32
-
-
0034100346
-
Allosteric interactions between the antagonist prazosin and amiloride analogs at the human alpha(1A)-adrenergic receptor
-
Leppik RA, Mynett A, Lazareno S, Birdsall NJ, (2000) Allosteric interactions between the antagonist prazosin and amiloride analogs at the human alpha(1A)-adrenergic receptor. Mol Pharmacol 57: 436-445.
-
(2000)
Mol Pharmacol
, vol.57
, pp. 436-445
-
-
Leppik, R.A.1
Mynett, A.2
Lazareno, S.3
Birdsall, N.J.4
-
33
-
-
0029807131
-
Phenylalanine in the second membrane-spanning domain of alpha 1A-adrenergic receptor determines subtype selectivity of dihydropyridine antagonists
-
Hamaguchi N, True TA, Saussy DL Jr, Jeffs PW, (1996) Phenylalanine in the second membrane-spanning domain of alpha 1A-adrenergic receptor determines subtype selectivity of dihydropyridine antagonists. Biochemistry 35: 14312-14317.
-
(1996)
Biochemistry
, vol.35
, pp. 14312-14317
-
-
Hamaguchi, N.1
True, T.A.2
Saussy Jr., D.L.3
Jeffs, P.W.4
-
34
-
-
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 PG, Cotecchia S, (1996) Amino acids of the alpha1B-adrenergic receptor involved in agonist binding: differences in docking catecholamines to receptor subtypes. FEBS Lett 399: 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
-
35
-
-
35348947909
-
Asp125 and Thr130 in transmembrane domain 3 are major sites of alpha1b-adrenergic receptor antagonist binding
-
Takahashi K, Hossain M, Ahmed M, Bhuiyan MA, Ohnuki T, et al. (2007) Asp125 and Thr130 in transmembrane domain 3 are major sites of alpha1b-adrenergic receptor antagonist binding. Biol Pharm Bull 30: 1891-1894.
-
(2007)
Biol Pharm Bull
, vol.30
, pp. 1891-1894
-
-
Takahashi, K.1
Hossain, M.2
Ahmed, M.3
Bhuiyan, M.A.4
Ohnuki, T.5
-
36
-
-
41849105443
-
Mutational analysis of the alpha 1a-adrenergic receptor binding pocket of antagonists by radioligand binding assay
-
Ahmed M, Hossain M, Bhuiyan MA, Ishiguro M, Tanaka T, et al. (2008) Mutational analysis of the alpha 1a-adrenergic receptor binding pocket of antagonists by radioligand binding assay. Biol Pharm Bull 31: 598-601.
-
(2008)
Biol Pharm Bull
, vol.31
, pp. 598-601
-
-
Ahmed, M.1
Hossain, M.2
Bhuiyan, M.A.3
Ishiguro, M.4
Tanaka, T.5
-
37
-
-
0034697157
-
Novel aromatic residues in transmembrane domains IV and V involved in agonist binding at alpha(1a)-adrenergic receptors
-
Waugh DJ, Zhao MM, Zuscik MJ, Perez DM, (2000) Novel aromatic residues in transmembrane domains IV and V involved in agonist binding at alpha(1a)-adrenergic receptors. J Biol Chem 275: 11698-11705.
-
(2000)
J Biol Chem
, vol.275
, pp. 11698-11705
-
-
Waugh, D.J.1
Zhao, M.M.2
Zuscik, M.J.3
Perez, D.M.4
-
38
-
-
0029866748
-
The unique nature of the serine interactions for alpha 1-adrenergic receptor agonist binding and activation
-
Hwa J, Perez DM, (1996) The unique nature of the serine interactions for alpha 1-adrenergic receptor agonist binding and activation. J Biol Chem 271: 6322-6327.
-
(1996)
J Biol Chem
, vol.271
, pp. 6322-6327
-
-
Hwa, J.1
Perez, D.M.2
-
39
-
-
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, et al. (1999) 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: 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
-
40
-
-
0029117219
-
Identification of critical determinants of alpha 1-adrenergic receptor subtype selective agonist binding
-
Hwa J, Graham RM, Perez DM, (1995) Identification of critical determinants of alpha 1-adrenergic receptor subtype selective agonist binding. J Biol Chem 270: 23189-23195.
-
(1995)
J Biol Chem
, vol.270
, pp. 23189-23195
-
-
Hwa, J.1
Graham, R.M.2
Perez, D.M.3
-
41
-
-
0035816665
-
Phe-308 and Phe-312 in transmembrane domain 7 are major sites of alpha 1-adrenergic receptor antagonist binding. Imidazoline agonists bind like antagonists
-
Waugh DJ, Gaivin RJ, Zuscik MJ, Gonzalez-Cabrera P, Ross SA, et al. (2001) Phe-308 and Phe-312 in transmembrane domain 7 are major sites of alpha 1-adrenergic receptor antagonist binding. Imidazoline agonists bind like antagonists. J Biol Chem 276: 25366-25371.
-
(2001)
J Biol Chem
, vol.276
, pp. 25366-25371
-
-
Waugh, D.J.1
Gaivin, R.J.2
Zuscik, M.J.3
Gonzalez-Cabrera, P.4
Ross, S.A.5
-
42
-
-
0030461873
-
Modeling and mutagenesis of the human alpha 1a-adrenoceptor: orientation and function of transmembrane helix V sidechains
-
Wetzel JM, Salon JA, Tamm JA, Forray C, Craig D, et al. (1996) Modeling and mutagenesis of the human alpha 1a-adrenoceptor: orientation and function of transmembrane helix V sidechains. Receptors Channels 4: 165-177.
-
(1996)
Receptors Channels
, vol.4
, pp. 165-177
-
-
Wetzel, J.M.1
Salon, J.A.2
Tamm, J.A.3
Forray, C.4
Craig, D.5
-
43
-
-
80053038272
-
Identification of essential cannabinoid-binding domains: structural insights into early dynamic events in receptor activation
-
Shim JY, Bertalovitz AC, Kendall DA, (2011) Identification of essential cannabinoid-binding domains: structural insights into early dynamic events in receptor activation. J Biol Chem 286: 33422-33435.
-
(2011)
J Biol Chem
, vol.286
, pp. 33422-33435
-
-
Shim, J.Y.1
Bertalovitz, A.C.2
Kendall, D.A.3
-
44
-
-
84880803392
-
Effects of rho-Da1a a peptidic alpha1a-adrenoceptor antagonist in human isolated prostatic adenoma and anesthetized rats
-
Palea S, Maiga A, Guilloteau V, Rekik M, Guerard M, et al. (2012) Effects of rho-Da1a a peptidic alpha1a-adrenoceptor antagonist in human isolated prostatic adenoma and anesthetized rats. Br J Pharmacol in press.
-
(2012)
Br J Pharmacol in Press
-
-
Palea, S.1
Maiga, A.2
Guilloteau, V.3
Rekik, M.4
Guerard, M.5
-
45
-
-
0141762594
-
Expression of EGFP-amino-tagged human mu opioid receptor in Drosophila Schneider 2 cells: a potential expression system for large-scale production of G-protein coupled receptors
-
Perret BG, Wagner R, Lecat S, Brillet K, Rabut G, et al. (2003) Expression of EGFP-amino-tagged human mu opioid receptor in Drosophila Schneider 2 cells: a potential expression system for large-scale production of G-protein coupled receptors. Protein Expression and Purification 31: 123-132.
-
(2003)
Protein Expression and Purification
, vol.31
, pp. 123-132
-
-
Perret, B.G.1
Wagner, R.2
Lecat, S.3
Brillet, K.4
Rabut, G.5
-
46
-
-
1542376711
-
Production of the Human D2S Receptor in the Methylotrophic Yeast P. pastoris?
-
Grunewald S, Haase W, Molsberger E, Michel H, Reilender H, (2004) Production of the Human D2S Receptor in the Methylotrophic Yeast P. pastoris? Receptors and Channels 10: 37-50.
-
(2004)
Receptors and Channels
, vol.10
, pp. 37-50
-
-
Grunewald, S.1
Haase, W.2
Molsberger, E.3
Michel, H.4
Reilender, H.5
-
47
-
-
27844519281
-
New concepts in drug discovery: collateral efficacy and permissive antagonism
-
Kenakin T, (2005) New concepts in drug discovery: collateral efficacy and permissive antagonism. Nat Rev Drug Discov 4: 919-927.
-
(2005)
Nat Rev Drug Discov
, vol.4
, pp. 919-927
-
-
Kenakin, T.1
-
48
-
-
77952354490
-
Seven transmembrane receptors as shapeshifting proteins: the impact of allosteric modulation and functional selectivity on new drug discovery
-
Kenakin T, Miller LJ, (2010) Seven transmembrane receptors as shapeshifting proteins: the impact of allosteric modulation and functional selectivity on new drug discovery. Pharmacol Rev 62: 265-304.
-
(2010)
Pharmacol Rev
, vol.62
, pp. 265-304
-
-
Kenakin, T.1
Miller, L.J.2
-
49
-
-
84863214200
-
Agonist-dependent modulation of arterial endothelinA receptor function
-
Compeer MG, Meens MJ, Hackeng TM, Neugebauer WA, Holtke C, et al. (2012) Agonist-dependent modulation of arterial endothelinA receptor function. Br J Pharmacol 166: 1833-1845.
-
(2012)
Br J Pharmacol
, vol.166
, pp. 1833-1845
-
-
Compeer, M.G.1
Meens, M.J.2
Hackeng, T.M.3
Neugebauer, W.A.4
Holtke, C.5
-
50
-
-
0029126526
-
Detection, quantitation, and verification of allosteric interactions of agents with labeled and unlabeled ligands at G protein-coupled receptors: interactions of strychnine and acetylcholine at muscarinic receptors
-
Lazareno S, Birdsall NJ, (1995) Detection, quantitation, and verification of allosteric interactions of agents with labeled and unlabeled ligands at G protein-coupled receptors: interactions of strychnine and acetylcholine at muscarinic receptors. Mol Pharmacol 48: 362-378.
-
(1995)
Mol Pharmacol
, vol.48
, pp. 362-378
-
-
Lazareno, S.1
Birdsall, N.J.2
-
51
-
-
0023263617
-
Identification of residues required for ligand binding to the beta-adrenergic receptor
-
Strader CD, Sigal IS, Register RB, Candelore MR, Rands E, et al. (1987) Identification of residues required for ligand binding to the beta-adrenergic receptor. Proc Natl Acad Sci U S A 84: 4384-4388.
-
(1987)
Proc Natl Acad Sci U S A
, vol.84
, pp. 4384-4388
-
-
Strader, C.D.1
Sigal, I.S.2
Register, R.B.3
Candelore, M.R.4
Rands, E.5
-
52
-
-
0029661256
-
Activation of the alpha1b-adrenergic receptor is initiated by disruption of an interhelical salt bridge constraint
-
Porter JE, Hwa J, Perez DM, (1996) Activation of the alpha1b-adrenergic receptor is initiated by disruption of an interhelical salt bridge constraint. J Biol Chem 271: 28318-28323.
-
(1996)
J Biol Chem
, vol.271
, pp. 28318-28323
-
-
Porter, J.E.1
Hwa, J.2
Perez, D.M.3
-
53
-
-
0034604451
-
Crystal structure of rhodopsin: A G protein-coupled receptor
-
Palczewski K, Kumasaka T, Hori T, Behnke CA, Motoshima H, et al. (2000) Crystal structure of rhodopsin: A G protein-coupled receptor. Science 289: 739-745.
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
Kumasaka, T.2
Hori, T.3
Behnke, C.A.4
Motoshima, H.5
-
54
-
-
84857254248
-
Crystal structure of a lipid G protein-coupled receptor
-
Hanson MA, Roth CB, Jo E, Griffith MT, Scott FL, et al. (2012) Crystal structure of a lipid G protein-coupled receptor. Science 335: 851-855.
-
(2012)
Science
, vol.335
, pp. 851-855
-
-
Hanson, M.A.1
Roth, C.B.2
Jo, E.3
Griffith, M.T.4
Scott, F.L.5
-
55
-
-
85027927015
-
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists
-
Wu B, Chien EY, Mol CD, Fenalti G, Liu W, et al. (2010) Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists. Science 330: 1066-1071.
-
(2010)
Science
, vol.330
, pp. 1066-1071
-
-
Wu, B.1
Chien, E.Y.2
Mol, C.D.3
Fenalti, G.4
Liu, W.5
-
56
-
-
34548476934
-
Critical role for the second extracellular loop in the binding of both orthosteric and allosteric G protein-coupled receptor ligands
-
Avlani VA, Gregory KJ, Morton CJ, Parker MW, Sexton PM, et al. (2007) Critical role for the second extracellular loop in the binding of both orthosteric and allosteric G protein-coupled receptor ligands. J Biol Chem 282: 25677-25686.
-
(2007)
J Biol Chem
, vol.282
, pp. 25677-25686
-
-
Avlani, V.A.1
Gregory, K.J.2
Morton, C.J.3
Parker, M.W.4
Sexton, P.M.5
-
57
-
-
77954141714
-
The three-finger toxin MTα is a selective α2B-adrenoceptor antagonist
-
Koivula K, Rondinelli S, Näsman J, (2010) The three-finger toxin MTα is a selective α2B-adrenoceptor antagonist. Toxicon 56: 440-447.
-
(2010)
Toxicon
, vol.56
, pp. 440-447
-
-
Koivula, K.1
Rondinelli, S.2
Näsman, J.3
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