-
1
-
-
33748671369
-
The 7 TM G protein-coupled receptor target family
-
Jacoby, E., Bouhelal, R., Gerspacher, M. & Seuwen, K. The 7 TM G protein-coupled receptor target family. ChemMedChem 1, 761-782 (2006).
-
(2006)
ChemMedChem
, vol.1
, pp. 761-782
-
-
Jacoby, E.1
Bouhelal, R.2
Gerspacher, M.3
Seuwen, K.4
-
2
-
-
84857375139
-
Allosteric modulation of seven transmembrane spanning receptors: Theory, practice, and opportunities for central nervous system drug discovery
-
Melancon, B. J. et al. Allosteric modulation of seven transmembrane spanning receptors: Theory, practice, and opportunities for central nervous system drug discovery. J. Biol. Chem. 55, 1445-1464 (2012).
-
(2012)
J. Biol. Chem.
, vol.55
, pp. 1445-1464
-
-
Melancon, B.J.1
-
3
-
-
77952354490
-
Seven transmembrane receptors as shapeshifting proteins: The impact of allosteric modulation and functional selectivity on new drug discovery
-
Kenakin, T. & Miller, L. J. Seven transmembrane receptors as shapeshifting proteins: The impact of allosteric modulation and functional selectivity on new drug discovery. Pharmacol. Rev. 62, 265-304 (2010).
-
(2010)
Pharmacol. Rev.
, vol.62
, pp. 265-304
-
-
Kenakin, T.1
Miller, L.J.2
-
4
-
-
84855879360
-
The best of both worlds? Biotopic orthosteric/allosteric ligands of G protein-coupled receptors
-
Valant, C., Lane, J. R., Sexon, P. M. & Christopoulos, A. The best of both worlds? Biotopic orthosteric/allosteric ligands of G protein-coupled receptors. Annu. Rev. Pharmacol. Toxicol. 52, 153-178 (2012).
-
(2012)
Annu. Rev. Pharmacol. Toxicol.
, vol.52
, pp. 153-178
-
-
Valant, C.1
Lane, J.R.2
Sexon, P.M.3
Christopoulos, A.4
-
5
-
-
59649112659
-
Dualsteric GPCR targeting: A novel route to binding and signaling pathway selectivity
-
Antony, J. et al. Dualsteric GPCR targeting: A novel route to binding and signaling pathway selectivity. FASEB J. 23, 442-450 (2009).
-
(2009)
FASEB J.
, vol.23
, pp. 442-450
-
-
Antony, J.1
-
6
-
-
34547208823
-
A novel multivalent ligand that bridges the allosteric and orthosteric binding sites of the M2 muscarinic receptor
-
Steinfeld, T., Mammen, M., Smith, J. A., Wilson, R. D. & Jasper, J. R. A novel multivalent ligand that bridges the allosteric and orthosteric binding sites of the M2 muscarinic receptor. Mol. Pharmacol. 72, 291-302 (2007).
-
(2007)
Mol. Pharmacol.
, vol.72
, pp. 291-302
-
-
Steinfeld, T.1
Mammen, M.2
Smith, J.A.3
Wilson, R.D.4
Jasper, J.R.5
-
7
-
-
57649170953
-
A novel mechanism of G protein-coupled receptor functional selectivity Muscarinic partial agonist McN A-343 as a bitopic orthosteric/allosteric ligand
-
Valant, C. et al. A novel mechanism of G protein-coupled receptor functional selectivity. Muscarinic partial agonist McN A-343 as a bitopic orthosteric/allosteric ligand. J. Biol. Chem. 283, 29312-29321 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 29312-29321
-
-
Valant, C.1
-
8
-
-
0028062082
-
Identification of drugs competing with d tubocurarine for an allosteric site on cardiac muscarinic receptors
-
Waelbroeck, M. Identification of drugs competing with d tubocurarine for an allosteric site on cardiac muscarinic receptors. Mol. Pharmacol. 46, 685-692 (1994).
-
(1994)
Mol. Pharmacol.
, vol.46
, pp. 685-692
-
-
Waelbroeck, M.1
-
9
-
-
0031588375
-
Pharmacological analysis of the mode of interaction of McN A-343 at atrial muscarinic M2 receptors
-
Christopoulos, A. & Mitchelson, F. Pharmacological analysis of the mode of interaction of McN A-343 at atrial muscarinic M2 receptors. Eur. J. Pharmacol. 339, 153-156 (1997).
-
(1997)
Eur. J. Pharmacol.
, vol.339
, pp. 153-156
-
-
Christopoulos, A.1
Mitchelson, F.2
-
10
-
-
77951223981
-
Identification of orthosteric and allosteric site mutations in the M2 muscarinic acetylcholine receptors that contribute to ligand-selective signalling bias
-
Gregory, K. J., Hall, N. E., Tobin, A. B., Sexton, P. M. & Christopoulos, A. Identification of orthosteric and allosteric site mutations in the M2 muscarinic acetylcholine receptors that contribute to ligand-selective signalling bias. J. Biol. Chem. 285, 7459-7474 (2010).
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 7459-7474
-
-
Gregory, K.J.1
Hall, N.E.2
Tobin, A.B.3
Sexton, P.M.4
Christopoulos, A.5
-
11
-
-
30044435787
-
Probing the molecular mechanism of interaction between 4 n butyl 1-[4-(2 methylphenyl)-4 oxo 1 butyl] piperidine (AC 42) and the muscarinic M1 receptor: Direct pharmacological evidence that AC 42 is an allosteric agonist
-
Langmead, C. J. et al. Probing the molecular mechanism of interaction between 4 n butyl 1-[4-(2 methylphenyl)-4 oxo 1 butyl]-piperidine (AC 42) and the muscarinic M1 receptor: Direct pharmacological evidence that AC 42 is an allosteric agonist. Mol. Pharmacol. 69, 236-246 (2006).
-
(2006)
Mol. Pharmacol.
, vol.69
, pp. 236-246
-
-
Langmead, C.J.1
-
12
-
-
77953777461
-
Orthosteric and allosteric modes of interaction of novel selective agonists of the M1 muscarinic acetylcholine receptor
-
Avlani, V. A. et al. Orthosteric and allosteric modes of interaction of novel selective agonists of the M1 muscarinic acetylcholine receptor. Mol. Pharmacol. 78, 94-104 (2010).
-
(2010)
Mol. Pharmacol.
, vol.78
, pp. 94-104
-
-
Avlani, V.A.1
-
13
-
-
59449090754
-
Mutageneic mapping suggests a novel binding mode for selective agonists of M1 muscarinic acetylcholine receptors
-
Lebon, G., Langmead, C. J., Tehan, B. G. & Hulme, E. C. Mutageneic mapping suggests a novel binding mode for selective agonists of M1 muscarinic acetylcholine receptors. Mol. Pharmacol. 75, 331-341 (2009).
-
(2009)
Mol. Pharmacol.
, vol.75
, pp. 331-341
-
-
Lebon, G.1
Langmead, C.J.2
Tehan, B.G.3
Hulme, E.C.4
-
14
-
-
78449305788
-
Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist
-
Chien, E. Y. et al. Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist. Science 330, 1091-1095 (2010).
-
(2010)
Science
, vol.330
, pp. 1091-1095
-
-
Chien, E.Y.1
-
15
-
-
30444436744
-
Design, syn thesis, and action of oxotremorine-related hybrid-type allosteric modulators of muscarinic acetylcholine receptors
-
Disingrini, T. et al. Design, synthesis, and action of oxotremorine-related hybrid-type allosteric modulators of muscarinic acetylcholine receptors. J. Med. Chem. 49, 366-372 (2006).
-
(2006)
J. Med. Chem.
, vol.49
, pp. 366-372
-
-
Disingrini, T.1
-
16
-
-
77951136172
-
Hybrid ortho/allosteric ligands for the adenosine A1 receptor
-
Narlawar, R. et al. Hybrid ortho/allosteric ligands for the adenosine A1 receptor. J. Med. Chem. 53, 3028-3037 (2010).
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3028-3037
-
-
Narlawar, R.1
-
17
-
-
0030218059
-
Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation
-
Kostenis, E. & Mohr, K. Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation. Trends Pharmacol. Sci. 17, 280-283 (1996).
-
(1996)
Trends Pharmacol. Sci.
, vol.17
, pp. 280-283
-
-
Kostenis, E.1
Mohr, K.2
-
18
-
-
33847122495
-
Allosteric modulation of G protein-coupled receptors
-
May, L. T., Leach, K., Sexton, P. M. & Christopoulos, A. Allosteric modulation of G protein-coupled receptors. Annu. Rev. Pharmacol. Toxicol. 47, 1-51 (2007).
-
(2007)
Annu. Rev. Pharmacol. Toxicol.
, vol.47
, pp. 1-51
-
-
May, L.T.1
Leach, K.2
Sexton, P.M.3
Christopoulos, A.4
-
19
-
-
0023958554
-
Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods
-
Ehlert, F. J. Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods. Mol. Pharmacol. 33, 187-194 (1988).
-
(1988)
Mol. Pharmacol.
, vol.33
, pp. 187-194
-
-
Ehlert, F.J.1
-
20
-
-
0021058380
-
Operational models of pharmacological agonism
-
Black, J. W. & Leff, P. Operational models of pharmacological agonism. Proc. R. Soc. B Biol. Sci. 220, 141-162 (1983).
-
(1983)
Proc. R. Soc. B Biol. Sci.
, vol.220
, pp. 141-162
-
-
Black, J.W.1
Leff, P.2
-
21
-
-
15744391870
-
The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor
-
Watson, C., Jenkinson, S., Kazmierski, W. & Kenakin, T. The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor. Mol. Pharmacol. 67, 1268-1282 (2005).
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 1268-1282
-
-
Watson, C.1
Jenkinson, S.2
Kazmierski, W.3
Kenakin, T.4
-
22
-
-
0031887759
-
Ivermectin: A positive allosteric effector of the α7 neuronal nicotinic acetylcholine receptor
-
Krause, R. M. et al. Ivermectin: A positive allosteric effector of the α7 neuronal nicotinic acetylcholine receptor. Mol. Pharmacol. 53, 283-294 (1998).
-
(1998)
Mol. Pharmacol.
, vol.53
, pp. 283-294
-
-
Krause, R.M.1
-
23
-
-
79952396557
-
Impact of species variability and 'probe-dependence' on the detection and in vivo validation of allosteric modulation at the M4 muscarinic acetylcholine receptor
-
Suratman, S. et al. Impact of species variability and 'probe-dependence' on the detection and in vivo validation of allosteric modulation at the M4 muscarinic acetylcholine receptor. Br. J. Pharmacol. 162, 1659-1670 (2011).
-
(2011)
Br. J. Pharmacol.
, vol.162
, pp. 1659-1670
-
-
Suratman, S.1
-
24
-
-
77953485027
-
Structural determinants of allosteric agonism and modulation at the M4 muscarinic acetylcholine receptor: Identification of ligand-specific and global activation mechanisms
-
Nawaratne, V., Leach, K., Felder, C. C., Sexton, P. M. & Christopoulos, A. Structural determinants of allosteric agonism and modulation at the M4 muscarinic acetylcholine receptor: Identification of ligand-specific and global activation mechanisms. J. Biol. Chem. 285, 19012-19021 (2010).
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 19012-19021
-
-
Nawaratne, V.1
Leach, K.2
Felder, C.C.3
Sexton, P.M.4
Christopoulos, A.5
-
25
-
-
84455173446
-
Probe dependence in the allosteric modulation of a G protein-coupled receptor: Implications for detection and validation of allosteric ligand effects
-
Valant, C., Felder, C. C., Sexton, P. M. & Christopoulos, A. Probe dependence in the allosteric modulation of a G protein-coupled receptor: Implications for detection and validation of allosteric ligand effects. Mol. Pharmacol. 81, 41-52 (2012).
-
(2012)
Mol. Pharmacol.
, vol.81
, pp. 41-52
-
-
Valant, C.1
Felder, C.C.2
Sexton, P.M.3
Christopoulos, A.4
-
26
-
-
49449108109
-
Allosteric modulation of the muscarinic M4 receptor as an approach to treating schizophrenia
-
Chan, W. Y. et al. Allosteric modulation of the muscarinic M4 receptor as an approach to treating schizophrenia. Proc. Natl Acad. Sci. USA 105, 10978-10983 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 10978-10983
-
-
Chan, W.Y.1
-
27
-
-
32144454172
-
The many roles of chemokines and chemokine receptors in inflammation
-
Charo, I. F. & Ransohoff, R. M. The many roles of chemokines and chemokine receptors in inflammation. N. Engl. J. Med. 354, 610-621 (2006).
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 610-621
-
-
Charo, I.F.1
Ransohoff, R.M.2
-
28
-
-
77955409173
-
The melanocortin 4 receptor: Physiology, pharmacology, and pathophysiology
-
Tao, Y. X. The melanocortin 4 receptor: Physiology, pharmacology, and pathophysiology. Endocr. Rev. 31, 506-543 (2010).
-
(2010)
Endocr. Rev.
, vol.31
, pp. 506-543
-
-
Tao, Y.X.1
-
29
-
-
0034332472
-
Interaction of PTH and PTHrP with their receptors
-
Gardella, T. J. & Juppner, H. Interaction of PTH and PTHrP with their receptors. Rev. Endocr. Metab. Disord. 1, 317-329 (2000).
-
(2000)
Rev. Endocr. Metab. Disord.
, vol.1
, pp. 317-329
-
-
Gardella, T.J.1
Juppner, H.2
-
30
-
-
33947324489
-
Relaxin family peptide receptors - Former orphans reunite with their parent ligands to activate multiple signalling pathways
-
Halls, M. L., van der Westhuizen, E. T., Bathgate, R. A. & Summers, R. J. Relaxin family peptide receptors - former orphans reunite with their parent ligands to activate multiple signalling pathways. Br. J. Pharmacol. 150, 677-691 (2007).
-
(2007)
Br. J. Pharmacol.
, vol.150
, pp. 677-691
-
-
Halls, M.L.1
Van Der Westhuizen, E.T.2
Bathgate, R.A.3
Summers, R.J.4
-
31
-
-
0034712831
-
Lamino acid sensing by the extracellular Ca2+-sensing receptor
-
Conigrave, A. D., Quinn, S. J. & Brown, E. M. lamino acid sensing by the extracellular Ca2+-sensing receptor. Br. J. Pharmacol. 97, 4814-4819 (2000).
-
(2000)
Br. J. Pharmacol.
, vol.97
, pp. 4814-4819
-
-
Conigrave, A.D.1
Quinn, S.J.2
Brown, E.M.3
-
32
-
-
0036266044
-
International union of pharmacology xxxii the mammalian calcitonin gene-related peptides, adrenomedullin, amylin, and calcitonin receptors
-
Poyner, D. R. et al. International Union of Pharmacology. XXXII. The mammalian calcitonin gene-related peptides, adrenomedullin, amylin, and calcitonin receptors. Pharmacol. Rev. 54, 233-246 (2002).
-
(2002)
Pharmacol. Rev.
, vol.54
, pp. 233-246
-
-
Poyner, D.R.1
-
33
-
-
33646512858
-
Glucagon and glucagon-like peptide receptors as drug targets
-
Estall, J. L. & Drucker, D. J. Glucagon and glucagon-like peptide receptors as drug targets. Curr. Pharm. Des. 12, 1731-1750 (2006).
-
(2006)
Curr. Pharm. Des.
, vol.12
, pp. 1731-1750
-
-
Estall, J.L.1
Drucker, D.J.2
-
34
-
-
34447632041
-
Allosteric GPCR modulators: Taking advantage of permissive receptor pharmacology
-
Leach, K., Sexton, P. M. & Christopoulos, A. Allosteric GPCR modulators: Taking advantage of permissive receptor pharmacology. Trends. Pharmacol. Sci. 28, 382-389 (2007).
-
(2007)
Trends. Pharmacol. Sci.
, vol.28
, pp. 382-389
-
-
Leach, K.1
Sexton, P.M.2
Christopoulos, A.3
-
35
-
-
0345735773
-
Agonist and inverse agonist actions of β-blockers at the human β2 adrenoceptor provide evidence for agonist-directed signaling
-
Baker, J. G., Hall, I. P. & Hill, S. J. Agonist and inverse agonist actions of β-blockers at the human β2 adrenoceptor provide evidence for agonist-directed signaling. Mol. Pharmacol. 64, 1357-1369 (2003).
-
(2003)
Mol. Pharmacol.
, vol.64
, pp. 1357-1369
-
-
Baker, J.G.1
Hall, I.P.2
Hill, S.J.3
-
36
-
-
36749094552
-
A unique mechanism of β-blocker action: Carvedilol stimulates β-arrestin signaling
-
Wisler, J. W. et al. A unique mechanism of β-blocker action: Carvedilol stimulates β-arrestin signaling. Proc. Natl Acad. Sci. USA 104, 16657-16662 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 16657-16662
-
-
Wisler, J.W.1
-
37
-
-
77955478709
-
A novel biased allosteric compound inhibitor of parturition selectively impedes the prostaglandin F2α mediated Rho/ROCK signaling pathway
-
Goupil, E. et al. A novel biased allosteric compound inhibitor of parturition selectively impedes the prostaglandin F2α mediated Rho/ROCK signaling pathway. J. Biol. Chem. 285, 25624-25636 (2010).
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 25624-25636
-
-
Goupil, E.1
-
38
-
-
34248393065
-
An acquired hypocalciuric hypercalcemia autoantibody induces allosteric transition among active human Ca sensing receptor conformations
-
Makita, N. et al. An acquired hypocalciuric hypercalcemia autoantibody induces allosteric transition among active human Ca sensing receptor conformations. Proc. Natl Acad. Sci. USA 104, 5443-5448 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 5443-5448
-
-
Makita, N.1
-
39
-
-
82355169577
-
Allostery In GPCRs: MWC' revisited
-
Canals, M., Sexton, P. M. & Christopoulos, A. Allostery in GPCRs: 'MWC' revisited. Trends. Biochem. Sci. 36, 663-672 (2011).
-
(2011)
Trends. Biochem. Sci.
, vol.36
, pp. 663-672
-
-
Canals, M.1
Sexton, P.M.2
Christopoulos, A.3
-
40
-
-
76749144987
-
Molecular mechanisms of action and in vivo validation of an M4 muscarinic acetylcholine receptor allosteric modulator with potential antipsychotic properties
-
Leach, K. et al. Molecular mechanisms of action and in vivo validation of an M4 muscarinic acetylcholine receptor allosteric modulator with potential antipsychotic properties. Neuropsychopharmacology 35, 855-869 (2010).
-
(2010)
Neuropsychopharmacology
, vol.35
, pp. 855-869
-
-
Leach, K.1
-
41
-
-
77956249652
-
Allosteric ligands of the glucagon-like peptide 1 receptor (GLP 1R) differentially modulate endogenous and exogenous peptide responses in a pathway-selective manner: Implications for drug screening
-
Koole, C. et al. Allosteric ligands of the glucagon-like peptide 1 receptor (GLP 1R) differentially modulate endogenous and exogenous peptide responses in a pathway-selective manner: Implications for drug screening. Mol. Pharmacol. 78, 456-465 (2010).
-
(2010)
Mol. Pharmacol.
, vol.78
, pp. 456-465
-
-
Koole, C.1
-
42
-
-
84863950667
-
Allosteric modulation of endogenous metabolites as an avenue for drug discovery
-
Wootten, D. et al. Allosteric modulation of endogenous metabolites as an avenue for drug discovery. Mol. Pharmacol. 82, 281-290 (2012).
-
(2012)
Mol. Pharmacol.
, vol.82
, pp. 281-290
-
-
Wootten, D.1
-
43
-
-
84869842165
-
Small molecule allosteric modulation of the glucagon-like peptide 1 receptor enhances the insulinotropic effect of oxyntomodulin
-
Willard, F. S. et al. Small molecule allosteric modulation of the glucagon-like peptide 1 receptor enhances the insulinotropic effect of oxyntomodulin. Mol. Pharmacol. 82, 1066-1073 (2012).
-
(2012)
Mol. Pharmacol.
, vol.82
, pp. 1066-1073
-
-
Willard, F.S.1
-
44
-
-
1942487860
-
Gastrointestinal satiety signals III Glucagon-like peptide 1, oxyntomodulin, peptide YY, and pancreatic polypeptide
-
Stanley, S., Wynne, K. & Bloom, S. Gastrointestinal satiety signals III. Glucagon-like peptide 1, oxyntomodulin, peptide YY, and pancreatic polypeptide. Am. J. Physiol. Gastrointest. Liver Physiol. 286, G693-G697 (2004).
-
(2004)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.286
-
-
Stanley, S.1
Wynne, K.2
Bloom, S.3
-
45
-
-
78650038239
-
Novel small molecule glucagon-like peptide 1 receptor agonist stimulates insulin secretion in rodents and from human islets
-
Sloop, K. W. et al. Novel small molecule glucagon-like peptide 1 receptor agonist stimulates insulin secretion in rodents and from human islets. Diabetes 59, 3099-3107 (2010).
-
(2010)
Diabetes
, vol.59
, pp. 3099-3107
-
-
Sloop, K.W.1
-
46
-
-
62149094752
-
The relative activity of function sparing" HIV 1 entry inhibitors on viral entry and CCR5 internalization: Is allosteric functional selectivity a valuable therapeutic property?
-
Muniz-Medina, V. M. et al. The relative activity of "function sparing" HIV 1 entry inhibitors on viral entry and CCR5 internalization: Is allosteric functional selectivity a valuable therapeutic property? Mol. Pharmacol. 75, 490-501 (2009).
-
(2009)
Mol. Pharmacol.
, vol.75
, pp. 490-501
-
-
Muniz-Medina, V.M.1
-
47
-
-
20044377204
-
The influence of CCL3L1 gene-containing segmental duplications on HIV 1/AIDS susceptibility
-
Gonzalez, E. et al. The influence of CCL3L1 gene-containing segmental duplications on HIV 1/AIDS susceptibility. Science 307, 1434-1440 (2005).
-
(2005)
Science
, vol.307
, pp. 1434-1440
-
-
Gonzalez, E.1
-
48
-
-
84869842165
-
Small molecule allosteric modulation of the glucagon-like peptide 1 receptor enhances the insulinotropic effect of oxyntomodulin
-
Willard, F. S. et al. Small molecule allosteric modulation of the glucagon-like peptide 1 receptor enhances the insulinotropic effect of oxyntomodulin. Mol. Pharmacol. 82, 1066-1073 (2012).
-
(2012)
Mol. Pharmacol.
, vol.82
, pp. 1066-1073
-
-
Willard, F.S.1
-
49
-
-
80051544311
-
Functionally biased modulation of A3 adenosine receptor agonist efficacy and potency by imidazoquinolinamine allosteric enhancers
-
Gao, Z. G. et al. Functionally biased modulation of A3 adenosine receptor agonist efficacy and potency by imidazoquinolinamine allosteric enhancers. Biochem. Pharmacol. 82, 658-668 (2011).
-
(2011)
Biochem. Pharmacol.
, vol.82
, pp. 658-668
-
-
Gao, Z.G.1
-
50
-
-
0028953577
-
Degradation of glucagon-like peptide 1 by human plasma in vitro yields an N terminally truncated peptide that is a major endogenous metabolite in vivo
-
Deacon, C. F., Johnsen, A. H. & Holst, J. J. Degradation of glucagon-like peptide 1 by human plasma in vitro yields an N terminally truncated peptide that is a major endogenous metabolite in vivo. J. Clin. Endocrinol. Metab. 80, 952-957 (1995).
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 952-957
-
-
Deacon, C.F.1
Johnsen, A.H.2
Holst, J.J.3
-
51
-
-
0011137292
-
Acetylcholine metabolism at nerve-endings
-
Birks, R. I. & Macintosh, F. C. Acetylcholine metabolism at nerve-endings. Br. Med. Bull. 13, 157-161 (1957).
-
(1957)
Br. Med. Bull.
, vol.13
, pp. 157-161
-
-
Birks, R.I.1
Macintosh, F.C.2
-
52
-
-
0022355979
-
Adenosine uptake, transport, and metabolism in human erythrocytes
-
Plagemann, P. G., Wohlhueter, R. M. & Kraupp, M. Adenosine uptake, transport, and metabolism in human erythrocytes. J. Cell. Physiol. 125, 330-336 (1985).
-
(1985)
J. Cell. Physiol.
, vol.125
, pp. 330-336
-
-
Plagemann, P.G.1
Wohlhueter, R.M.2
Kraupp, M.3
-
53
-
-
0021903287
-
The concentration of choline and the activities of cholinesterases, creatine kinase and lactate dehydrogenase in the blood plasma of piglets with the syndrome of splayleg (congenital myofibrillar hypoplasia)
-
Tucek, S. et al. The concentration of choline and the activities of cholinesterases, creatine kinase and lactate dehydrogenase in the blood plasma of piglets with the syndrome of splayleg (congenital myofibrillar hypoplasia). Zentralbl. Veterinarmed. A 32, 1-10 (1985).
-
(1985)
Zentralbl. Veterinarmed.
, vol.A 32
, pp. 1-10
-
-
Tucek, S.1
-
54
-
-
0037372429
-
Cardiac outflow of amino acids and purines during myocardial ischemia and reperfusion
-
Backstrom, T., Goiny, M., Lockowandt, U., Liska, J. & Franco-Cereceda, A. Cardiac outflow of amino acids and purines during myocardial ischemia and reperfusion. J. Appl. Physiol. 94, 1122-1128 (2003).
-
(2003)
J. Appl. Physiol.
, vol.94
, pp. 1122-1128
-
-
Backstrom, T.1
Goiny, M.2
Lockowandt, U.3
Liska, J.4
Franco-Cereceda, A.5
-
55
-
-
77955028664
-
GLP 1 9- 36) amide metabolite suppression of glucose production in isolated mouse hepatocytes
-
Tomas, E., Stanojevic, V. & Habener, J. F. GLP 1 (9-36) amide metabolite suppression of glucose production in isolated mouse hepatocytes. Horm. Metab. Res. 42, 657-662 (2010).
-
(2010)
Horm. Metab. Res.
, vol.42
, pp. 657-662
-
-
Tomas, E.1
Stanojevic, V.2
Habener, J.F.3
-
56
-
-
84855290525
-
A Monod-Wyman-Changeux mechanism can explain G protein-coupled receptor (GPCR) allosteric modulation
-
Canals, M. et al. A Monod-Wyman-Changeux mechanism can explain G protein-coupled receptor (GPCR) allosteric modulation. J. Biol. Chem. 287, 650-659 (2012).
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 650-659
-
-
Canals, M.1
-
57
-
-
77953661232
-
Re exploration of the PHCCC scaffold: Discovery of improved positive allosteric modulators of mGluR4
-
Williams, R. et al. Re exploration of the PHCCC scaffold: Discovery of improved positive allosteric modulators of mGluR4. ACS Chem. Neurosci. 1, 411-419 (2010).
-
(2010)
ACS Chem. Neurosci.
, vol.1
, pp. 411-419
-
-
Williams, R.1
-
58
-
-
78650379605
-
Chemical switch of a metabotropic glutamate receptor 2 silent allosteric modulator into dual metabotropic glutamate receptor 2/3 negative/positive allosteric modulators
-
Schann, S. et al. Chemical switch of a metabotropic glutamate receptor 2 silent allosteric modulator into dual metabotropic glutamate receptor 2/3 negative/positive allosteric modulators. J. Med. Chem. 53, 8775-8779 (2010).
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8775-8779
-
-
Schann, S.1
-
59
-
-
72249109559
-
Chemical lead optimization of a pan Gq mAChR M1 M3, M5 positive allosteric modulator (PAM) lead Part I: Development of the first highly selective M5 PAM
-
Bridges, T. M. et al. Chemical lead optimization of a pan Gq mAChR M1, M3, M5 positive allosteric modulator (PAM) lead. Part I: Development of the first highly selective M5 PAM. Bioorg. Med. Chem. Lett. 20, 558-562 (2010).
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 558-562
-
-
Bridges, T.M.1
-
60
-
-
84855961050
-
Discovery and development of a second highly selective m1 positive allosteric modulator (pam)
-
[online] (National Center for Biotechnology Information, 2010
-
Bridges, T. M. et al. Discovery and development of a second highly selective M1 positive allosteric modulator (PAM). Probe Reports from the NIH Molecular Libraries Program [online], http://www.ncbi.nlm.nih.gov/books/ NBK50704/ (National Center for Biotechnology Information, 2010).
-
Probe Reports From The NIH Molecular Libraries Program
-
-
Bridges, T.M.1
-
61
-
-
79955023104
-
Deal watch: Valuation benefits of structure-enabled drug discovery
-
Borshell, N., Papp, T. & Congreve, M. Deal watch: Valuation benefits of structure-enabled drug discovery. Nature Rev. Drug Discov. 10, 166 (2011).
-
(2011)
Nature Rev. Drug Discov.
, vol.10
, pp. 166
-
-
Borshell, N.1
Papp, T.2
Congreve, M.3
-
62
-
-
42149181885
-
Structural diversity of G protein-coupled receptors and significance for drug discovery
-
Lagerstrom, M. C. & Schioth, H. B. Structural diversity of G protein-coupled receptors and significance for drug discovery. Nature Rev. Drug Discov. 7, 339-357 (2008).
-
(2008)
Nature Rev. Drug Discov.
, vol.7
, pp. 339-357
-
-
Lagerstrom, M.C.1
Schioth, H.B.2
-
63
-
-
0034604451
-
Crystal structure of rhodopsin: A G protein-coupled receptor
-
Palczewski, K. et al. Crystal structure of rhodopsin: A G protein-coupled receptor. Science 289, 739-745 (2000).
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
-
64
-
-
80051658642
-
Crystal structure of the β2 adrenergic receptor Gs protein complex
-
Rasmussen, S. G. et al. Crystal structure of the β2 adrenergic receptor Gs protein complex. Nature 477, 549-555 (2011).
-
(2011)
Nature
, vol.477
, pp. 549-555
-
-
Rasmussen, S.G.1
-
65
-
-
84861064804
-
Crystal structures of a stabilized β1 adrenoceptor bound to the biased agonists bucindolol and carvedilol
-
Warne, T., Edwards, P. C., Leslie, A. G. & Tate, C. G. Crystal structures of a stabilized β1 adrenoceptor bound to the biased agonists bucindolol and carvedilol. Structure 20, 841-849 (2012).
-
(2012)
Structure
, vol.20
, pp. 841-849
-
-
Warne, T.1
Edwards, P.C.2
Leslie, A.G.3
Tate, C.G.4
-
66
-
-
84863115467
-
Structure and dynamics of the M3 muscarinic acetylcholine receptor
-
Kruse, A. C. et al. Structure and dynamics of the M3 muscarinic acetylcholine receptor. Nature 482, 552-556 (2012).
-
(2012)
Nature
, vol.482
, pp. 552-556
-
-
Kruse, A.C.1
-
67
-
-
84862777405
-
Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist
-
Haga, K. et al. Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist. Nature 482, 547-551 (2012).
-
(2012)
Nature
, vol.482
, pp. 547-551
-
-
Haga, K.1
-
68
-
-
84861075468
-
Structure of the δ-opioid receptor bound to naltrindole
-
Granier, S. et al. Structure of the δ-opioid receptor bound to naltrindole. Nature 485, 400-404 (2012).
-
(2012)
Nature
, vol.485
, pp. 400-404
-
-
Granier, S.1
-
69
-
-
84862777742
-
Structure of the human κ-opioid receptor in complex with JDTic
-
Wu, H. et al. Structure of the human κ-opioid receptor in complex with JDTic. Nature 485, 327-332 (2012).
-
(2012)
Nature
, vol.485
, pp. 327-332
-
-
Wu, H.1
-
70
-
-
79954782236
-
Structure of an agonist-bound human A2A adenosine receptor
-
Xu, F. et al. Structure of an agonist-bound human A2A adenosine receptor. Science 332, 322-327 (2011).
-
(2011)
Science
, vol.332
, pp. 322-327
-
-
Xu, F.1
-
71
-
-
79959564813
-
Agonist-bound adenosine A2A receptor structures reveal common features of GPCR activation
-
Lebon, G. et al. Agonist-bound adenosine A2A receptor structures reveal common features of GPCR activation. Nature 474, 521-525 (2011).
-
(2011)
Nature
, vol.474
, pp. 521-525
-
-
Lebon, G.1
-
72
-
-
84871411930
-
High-resolution crystal structure of human protease-activated receptor 1
-
Zhang, C. et al. High-resolution crystal structure of human protease-activated receptor 1. Nature 492, 387-392 (2012).
-
(2012)
Nature
, vol.492
, pp. 387-392
-
-
Zhang, C.1
-
73
-
-
85027927015
-
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists
-
Wu, B. et al. Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists. Science 330, 1066-1071 (2010).
-
(2010)
Science
, vol.330
, pp. 1066-1071
-
-
Wu, B.1
-
74
-
-
79960070651
-
Structure of the human histamine H1 receptor complex with doxepin
-
Shimamura, T. et al. Structure of the human histamine H1 receptor complex with doxepin. Nature 475, 65-70 (2011).
-
(2011)
Nature
, vol.475
, pp. 65-70
-
-
Shimamura, T.1
-
75
-
-
45549086826
-
Crystal structure of the ligand-bound glucagon-like peptide 1 receptor extracellular domain
-
Runge, S., Thogersen, H., Madsen, K., Lau, J. & Rudolph, R. Crystal structure of the ligand-bound glucagon-like peptide 1 receptor extracellular domain. J. Biol. Chem. 283, 11340-11347 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 11340-11347
-
-
Runge, S.1
Thogersen, H.2
Madsen, K.3
Lau, J.4
Rudolph, R.5
-
76
-
-
57749102733
-
Molecular recognition of corticotropin-releasing factor by its G protein-coupled receptor CRFR1
-
Pioszak, A. A., Parker, N. R., Suino-Powell, K. & Xu, H. E. Molecular recognition of corticotropin-releasing factor by its G protein-coupled receptor CRFR1. J. Biol. Chem. 283, 32900-32912 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 32900-32912
-
-
Pioszak, A.A.1
Parker, N.R.2
Suino-Powell, K.3
Xu, H.E.4
-
77
-
-
0037022586
-
Structural views of the ligand-binding cores of a metabotropic glutamate receptor complexed with an antagonist and both glutamate and Gd3+
-
Tsuchiya, D., Kunishima, N., Kamiya, N., Jingami, H. & Morikawa, K. Structural views of the ligand-binding cores of a metabotropic glutamate receptor complexed with an antagonist and both glutamate and Gd3+. Proc. Natl Acad. Sci. USA 99, 2660-2665 (2002).
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 2660-2665
-
-
Tsuchiya, D.1
Kunishima, N.2
Kamiya, N.3
Jingami, H.4
Morikawa, K.5
-
78
-
-
34247210665
-
Structures of the extracellular regions of the group II/III metabotropic glutamate receptors
-
Muto, T., Tsuchiya, D., Morikawa, K. & Jingami, H. Structures of the extracellular regions of the group II/III metabotropic glutamate receptors. Proc. Natl Acad. Sci. USA 104, 3759-3764 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 3759-3764
-
-
Muto, T.1
Tsuchiya, D.2
Morikawa, K.3
Jingami, H.4
-
79
-
-
0028815463
-
Probing of the location of the allosteric site on M1 muscarinic receptors by site-directed mutagenesis
-
Matsui, H., Lazareno, S. & Birdsall, N. J. Probing of the location of the allosteric site on M1 muscarinic receptors by site-directed mutagenesis. Mol. Pharmacol. 47, 88-98 (1995).
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 88-98
-
-
Matsui, H.1
Lazareno, S.2
Birdsall, N.J.3
-
80
-
-
0038575799
-
Interactions of orthosteric and allosteric ligands with [3H]dimethyl W84 at the common allosteric site of muscarinic M2 receptors
-
Trankle, C. et al. Interactions of orthosteric and allosteric ligands with [3H]dimethyl W84 at the common allosteric site of muscarinic M2 receptors. Mol. Pharmacol. 64, 180-190 (2003).
-
(2003)
Mol. Pharmacol.
, vol.64
, pp. 180-190
-
-
Trankle, C.1
-
81
-
-
33745282128
-
Allosteric interactions with muscarinic acetylcholine receptors: Complex role of the conserved tryptophan M2422Trp in a critical cluster of amino acids for baseline affinity, subtype selectivity, and cooperativity
-
Prilla, S., Schrobang, J., Ellis, J., Holtje, H. D. & Mohr, K. Allosteric interactions with muscarinic acetylcholine receptors: Complex role of the conserved tryptophan M2422Trp in a critical cluster of amino acids for baseline affinity, subtype selectivity, and cooperativity. Mol. Pharmacol. 70, 181-193 (2006).
-
(2006)
Mol. Pharmacol.
, vol.70
, pp. 181-193
-
-
Prilla, S.1
Schrobang, J.2
Ellis, J.3
Holtje, H.D.4
Mohr, K.5
-
82
-
-
34548476934
-
Critical role for the second extracellular loop in the binding of both orthosteric and allosteric G protein-coupled receptor ligands
-
Avlani, V. A. et al. 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).
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 25677-25686
-
-
Avlani, V.A.1
-
83
-
-
0034625144
-
A binding pocket for a small molecule inhibitor of HIV 1 entry within the transmembrane helices of CCR5
-
Dragic, T. et al. A binding pocket for a small molecule inhibitor of HIV 1 entry within the transmembrane helices of CCR5. Proc. Natl Acad. Sci. USA 97, 5639-5644 (2000).
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 5639-5644
-
-
Dragic, T.1
-
84
-
-
0035957911
-
Molecular interactions of cyclam and bicyclam non-peptide antagonists with the CXCR4 chemokine receptor
-
Gerlach, L. O., Skerlj, R. T., Bridger, G. J. & Schwartz, T. W. Molecular interactions of cyclam and bicyclam non-peptide antagonists with the CXCR4 chemokine receptor. J. Biol. Chem. 276, 14153-14160 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 14153-14160
-
-
Gerlach, L.O.1
Skerlj, R.T.2
Bridger, G.J.3
Schwartz, T.W.4
-
85
-
-
33744954776
-
Structural and molecular interactions of CCR5 inhibitors with CCR5
-
Maeda, K. et al. Structural and molecular interactions of CCR5 inhibitors with CCR5. J. Biol. Chem. 281, 12688-12698 (2006).
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 12688-12698
-
-
Maeda, K.1
-
86
-
-
54349117013
-
Identification of a putative intracellular allosteric antagonist binding-site in the CXC chemokine receptors 1 and 2
-
Nicholls, D. J. et al. Identification of a putative intracellular allosteric antagonist binding-site in the CXC chemokine receptors 1 and 2. Mol. Pharmacol. 74, 1193-1202 (2008).
-
(2008)
Mol. Pharmacol.
, vol.74
, pp. 1193-1202
-
-
Nicholls, D.J.1
-
87
-
-
40849124250
-
An intracellular allosteric site for a specific class of antagonists of the CC chemokine G protein-coupled receptors CCR4 and CCR5
-
Andrews, G., Jones, C. & Wreggett, K. A. An intracellular allosteric site for a specific class of antagonists of the CC chemokine G protein-coupled receptors CCR4 and CCR5. Mol. Pharmacol. 73, 855-867 (2008).
-
(2008)
Mol. Pharmacol.
, vol.73
, pp. 855-867
-
-
Andrews, G.1
Jones, C.2
Wreggett, K.A.3
-
88
-
-
0030731863
-
Localization of agonist- and antagonist-binding domains of human corticotropin-releasing factor receptors
-
Liaw, C. W., Grigoriadis, D. E., Lorang, M. T., De Souza, E. B. & Maki, R. A. Localization of agonist- and antagonist-binding domains of human corticotropin-releasing factor receptors. Mol. Endocrinol. 11, 2048-2053 (1997).
-
(1997)
Mol. Endocrinol.
, vol.11
, pp. 2048-2053
-
-
Liaw, C.W.1
Grigoriadis, D.E.2
Lorang, M.T.3
De Souza, E.B.4
Maki, R.A.5
-
89
-
-
33751082960
-
Point mutations in the transmembrane region of GABAB2 facilitate activation by the positive modulator N,NŶ dicyclopentyl-2 methylsulfanyl-5 nitro-pyrimidine 4,6 diamine (GS39783) in the absence of the GABAB1 subunit
-
Dupuis, D. S., Relkovic, D., Lhuillier, L., Mosbacher, J. & Kaupmann, K. Point mutations in the transmembrane region of GABAB2 facilitate activation by the positive modulator N,NŶ dicyclopentyl-2 methylsulfanyl-5 nitro-pyrimidine 4,6 diamine (GS39783) in the absence of the GABAB1 subunit. Mol. Pharmacol. 70, 2027-2036 (2006).
-
(2006)
Mol. Pharmacol.
, vol.70
, pp. 2027-2036
-
-
Dupuis, D.S.1
Relkovic, D.2
Lhuillier, L.3
Mosbacher, J.4
Kaupmann, K.5
-
90
-
-
0034721795
-
The non-competitive antagonists 2 methyl 6-(phenylethynyl)pyridine and 7 hydroxyiminocyclopropan[b]chromen-1a carboxylic acid ethyl ester interact with overlapping binding pockets in the transmembrane region of group I metabotropic glutamate receptors
-
Pagano, A. et al. The non-competitive antagonists 2 methyl 6-(phenylethynyl)pyridine and 7 hydroxyiminocyclopropan[b]chromen-1a carboxylic acid ethyl ester interact with overlapping binding pockets in the transmembrane region of group I metabotropic glutamate receptors. J. Biol. Chem. 275, 33750-33758 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 33750-33758
-
-
Pagano, A.1
-
91
-
-
0035818605
-
Positive allosteric modulators of metabotropic glutamate 1 receptor: Characterization, mechanism of action, and binding site
-
Knoflach, F. et al. Positive allosteric modulators of metabotropic glutamate 1 receptor: Characterization, mechanism of action, and binding site. Proc. Natl Acad. Sci. USA 98, 13402-13407 (2001).
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 13402-13407
-
-
Knoflach, F.1
-
92
-
-
1442358771
-
Modeling and mutagenesis of the binding site of Calhex 231, a novel negative allosteric modulator of the extracellular Ca2+-sensing receptor
-
Petrel, C. et al. Modeling and mutagenesis of the binding site of Calhex 231, a novel negative allosteric modulator of the extracellular Ca2+-sensing receptor. J. Biol. Chem. 278, 49487-49494 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 49487-49494
-
-
Petrel, C.1
-
93
-
-
0037424518
-
Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glutamate 1 receptor
-
Malherbe, P. et al. Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glutamate 1 receptor. J. Biol. Chem. 278, 8340-8347 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 8340-8347
-
-
Malherbe, P.1
-
94
-
-
1342346546
-
Homology modeling of the transmembrane domain of the human calcium sensing receptor and localization of an allosteric binding site
-
Miedlich, S. U., Gama, L., Seuwen, K., Wolf, R. M. & Breitwieser, G. E. Homology modeling of the transmembrane domain of the human calcium sensing receptor and localization of an allosteric binding site. J. Biol. Chem. 279, 7254-7263 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7254-7263
-
-
Miedlich, S.U.1
Gama, L.2
Seuwen, K.3
Wolf, R.M.4
Breitwieser, G.E.5
-
95
-
-
80052443569
-
Targeting protease-activated receptor 1 with cell-penetrating pepducins in lung cancer
-
Cisowski, J. et al. Targeting protease-activated receptor 1 with cell-penetrating pepducins in lung cancer. Am. J. Pathol. 179, 513-523 (2011).
-
(2011)
Am. J. Pathol.
, vol.179
, pp. 513-523
-
-
Cisowski, J.1
-
96
-
-
79551584772
-
Pharmacology, biodistribution, and efficacy of GPCR-based pepducins in disease models
-
Tressel, S. L. et al. Pharmacology, biodistribution, and efficacy of GPCR-based pepducins in disease models. Methods Mol. Biol. 683, 259-275 (2011).
-
(2011)
Methods Mol. Biol.
, vol.683
, pp. 259-275
-
-
Tressel, S.L.1
-
97
-
-
78651399683
-
Structure and function of an irreversible agonist-β2 adrenoceptor complex
-
Rosenbaum, D. M. et al. Structure and function of an irreversible agonist-β2 adrenoceptor complex. Nature 469, 236-240 (2011).
-
(2011)
Nature
, vol.469
, pp. 236-240
-
-
Rosenbaum, D.M.1
-
98
-
-
78651411166
-
Structure of a nanobody-stabilized active state of the β2 adrenoceptor
-
Rasmussen, S. G. et al. Structure of a nanobody-stabilized active state of the β2 adrenoceptor. Nature 469, 175-180 (2011).
-
(2011)
Nature
, vol.469
, pp. 175-180
-
-
Rasmussen, S.G.1
-
99
-
-
0025642404
-
An aspartate conserved among G protein receptors confers allosteric regulation of alpha 2 adrenergic receptors by sodium
-
Horstman, D. A. et al. An aspartate conserved among G protein receptors confers allosteric regulation of alpha 2 adrenergic receptors by sodium. J. Biol. Chem. 265, 21590-21595 (1990).
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 21590-21595
-
-
Horstman, D.A.1
-
100
-
-
0025238655
-
Spontaneous association between opioid receptors and GTP-binding regulatory proteins in native membranes: Specific regulation by antagonists and sodium ions
-
Costa, T., Lang, J., Gless, C. & Herz, A. Spontaneous association between opioid receptors and GTP-binding regulatory proteins in native membranes: Specific regulation by antagonists and sodium ions. Mol. Pharmacol. 37, 383-394 (1990).
-
(1990)
Mol. Pharmacol.
, vol.37
, pp. 383-394
-
-
Costa, T.1
Lang, J.2
Gless, C.3
Herz, A.4
-
101
-
-
0034284626
-
Allosteric modulation of A2A adenosine receptors by amiloride analogues and sodium ions
-
Gao, Z. G. & Ijzerman, A. P. Allosteric modulation of A2A adenosine receptors by amiloride analogues and sodium ions. Biochem. Pharmacol. 60, 669-676 (2000).
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 669-676
-
-
Gao, Z.G.1
Ijzerman, A.P.2
-
102
-
-
78049415021
-
Induced effects of sodium ions on dopaminergic G protein coupled receptors
-
Selent, J., Sanz, F., Pastor, M. & De Fabritiis, G. Induced effects of sodium ions on dopaminergic G protein coupled receptors. PLoS Comput. Biol. 6, e1000884 (2010).
-
(2010)
PLoS Comput. Biol.
, vol.6
-
-
Selent, J.1
Sanz, F.2
Pastor, M.3
De Fabritiis, G.4
-
103
-
-
0034918454
-
Modeling and mutational analysis of a putative sodium-binding pocket on the dopamine D2 receptor
-
Neve, K. A. et al. Modeling and mutational analysis of a putative sodium-binding pocket on the dopamine D2 receptor. Mol. Pharmacol. 60, 373-381 (2001).
-
(2001)
Mol. Pharmacol.
, vol.60
, pp. 373-381
-
-
Neve, K.A.1
-
104
-
-
46549083395
-
An ion-responsive motif in the second transmembrane segment of rhodopsin-like receptors
-
Parker, M. S., Wong, Y. Y. & Parker, S. L. An ion-responsive motif in the second transmembrane segment of rhodopsin-like receptors. Amino Acids 35, 1-15 (2008).
-
(2008)
Amino Acids
, vol.35
, pp. 1-15
-
-
Parker, M.S.1
Wong, Y.Y.2
Parker, S.L.3
-
105
-
-
78651297517
-
GPCRDB: Information system for G protein-coupled receptors
-
Vroling, B. et al. GPCRDB: Information system for G protein-coupled receptors. Nucleic Acids Res. 39, D309-D319 (2011).
-
(2011)
Nucleic Acids Res.
, vol.39
-
-
Vroling, B.1
-
106
-
-
84861961427
-
Structural basis for allosteric regulation of GPCRs by sodium ions
-
Liu, W. et al. Structural basis for allosteric regulation of GPCRs by sodium ions. Science 337, 232-236 (2012).
-
(2012)
Science
, vol.337
, pp. 232-236
-
-
Liu, W.1
-
107
-
-
79953242234
-
The structural basis of agonist-induced activation in constitutively active rhodopsin
-
Standfuss, J. et al. The structural basis of agonist-induced activation in constitutively active rhodopsin. Nature 471, 656-660 (2011).
-
(2011)
Nature
, vol.471
, pp. 656-660
-
-
Standfuss, J.1
-
108
-
-
0034616021
-
Receptors for dopamine and somatostatin: Formation of hetero-oligomers with enhanced functional activity
-
Rocheville, M. et al. Receptors for dopamine and somatostatin: Formation of hetero-oligomers with enhanced functional activity. Science 288, 154-157 (2000).
-
(2000)
Science
, vol.288
, pp. 154-157
-
-
Rocheville, M.1
-
109
-
-
13444274883
-
Evidence for negative binding cooperativity within CCR5-CCR2b heterodimers
-
El Asmar, L. et al. Evidence for negative binding cooperativity within CCR5-CCR2b heterodimers. Mol. Pharmacol. 67, 460-469 (2005).
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 460-469
-
-
El Asmar, L.1
-
110
-
-
33846030175
-
Orexin 1 receptor-cannabinoid CB1 receptor heterodimerization results in both ligand-dependent and -independent coordinated alterations of receptor localization and function
-
Ellis, J., Pediani, J. D., Canals, M., Milasta, S. & Milligan, G. Orexin 1 receptor-cannabinoid CB1 receptor heterodimerization results in both ligand-dependent and -independent coordinated alterations of receptor localization and function. J. Biol. Chem. 281, 38812-38824 (2006).
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 38812-38824
-
-
Ellis, J.1
Pediani, J.D.2
Canals, M.3
Milasta, S.4
Milligan, G.5
-
111
-
-
84868585481
-
Glucagon-like peptide 1 receptor dimerization differentially regulates agonist signaling but does not affect small molecule allostery
-
Harikumar, K. G. et al. Glucagon-like peptide 1 receptor dimerization differentially regulates agonist signaling but does not affect small molecule allostery. Proc. Natl Acad. Sci. USA 109, 18607-18612 (2012).
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. 18607-18612
-
-
Harikumar, K.G.1
-
112
-
-
77955841797
-
Importance of lipid-exposed residues in transmembrane segment four for family B calcitonin receptor homo-dimerization
-
Harikumar, K. G., Ball, A. M., Sexton, P. M. & Miller, L. J. Importance of lipid-exposed residues in transmembrane segment four for family B calcitonin receptor homo-dimerization. Regul. Pept. 164, 113-119 (2010).
-
(2010)
Regul. Pept.
, vol.164
, pp. 113-119
-
-
Harikumar, K.G.1
Ball, A.M.2
Sexton, P.M.3
Miller, L.J.4
-
113
-
-
54049088494
-
Dimerization in the absence of higher-order oligomerization of the G protein-coupled secretin receptor
-
Harikumar, K. G., Happs, R. M. & Miller, L. J. Dimerization in the absence of higher-order oligomerization of the G protein-coupled secretin receptor. Biochim. Biophys. Acta. 1778, 2555-2563 (2008).
-
(2008)
Biochim. Biophys. Acta.
, vol.1778
, pp. 2555-2563
-
-
Harikumar, K.G.1
Happs, R.M.2
Miller, L.J.3
-
114
-
-
35649028687
-
Transmembrane segment IV contributes a functionally important interface for oligomerization of the class II G protein-coupled secretin receptor
-
Harikumar, K. G., Pinon, D. I. & Miller, L. J. Transmembrane segment IV contributes a functionally important interface for oligomerization of the class II G protein-coupled secretin receptor. J. Biol. Chem. 282, 30363-30372 (2007).
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 30363-30372
-
-
Harikumar, K.G.1
Pinon, D.I.2
Miller, L.J.3
-
115
-
-
67650799169
-
Functional importance of a structurally distinct homodimeric complex of the family B G protein-coupled secretin receptor
-
Gao, F. et al. Functional importance of a structurally distinct homodimeric complex of the family B G protein-coupled secretin receptor. Mol. Pharmacol. 76, 264-274 (2009).
-
(2009)
Mol. Pharmacol.
, vol.76
, pp. 264-274
-
-
Gao, F.1
-
116
-
-
84867045173
-
Distinct roles of metabotropic glutamate receptor dimerization in agonist activation and G protein coupling
-
El Moustaine, D. et al. Distinct roles of metabotropic glutamate receptor dimerization in agonist activation and G protein coupling. Proc. Natl Acad. Sci. USA 109, 16342-16347 (2012).
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. 16342-16347
-
-
El Moustaine, D.1
-
117
-
-
11144353767
-
Cinacalcet for secondary hyperparathyroidism in patients receiving hemodialysis
-
Block, G. et al. Cinacalcet for secondary hyperparathyroidism in patients receiving hemodialysis. N. Engl. J. Med. 350, 1516-1525 (2004).
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 1516-1525
-
-
Block, G.1
-
118
-
-
33846429183
-
Clinical lessons from the calcium sensing receptor
-
Brown, E. M. Clinical lessons from the calcium sensing receptor. Nature Clin. Pract. Endocrinol. Metab. 3, 122-133 (2007).
-
(2007)
Nature Clin. Pract. Endocrinol. Metab.
, vol.3
, pp. 122-133
-
-
Brown, E.M.1
-
119
-
-
30744447460
-
Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV 1
-
Fatkenheuer, G. et al. Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV 1. Nature Med. 11, 1170-1172 (2005).
-
(2005)
Nature Med.
, vol.11
, pp. 1170-1172
-
-
Fatkenheuer, G.1
-
120
-
-
27744548649
-
The discovery of the CCR5 receptor antagonist UK 427 ,857, a new agent for the treatment of HIV infection and AIDS
-
Wood, A. & Armour, D. The discovery of the CCR5 receptor antagonist, UK 427,857, a new agent for the treatment of HIV infection and AIDS. Prog. Med. Chem. 43, 239-271 (2005).
-
(2005)
Prog. Med. Chem.
, Issue.43
, pp. 239-271
-
-
Wood, A.1
Armour, D.2
|