-
1
-
-
3843131055
-
Gonadotropin-releasing hormone receptors
-
Millar, R. P., Lu, Z. L., Pawson, A. J., Flanagan, C. A., Morgan, K., and Maudsley, S. R. (2004) Gonadotropin-releasing hormone receptors. Endocr. Rev. 25, 235-275.
-
(2004)
Endocr. Rev
, vol.25
, pp. 235-275
-
-
Millar, R.P.1
Lu, Z.L.2
Pawson, A.J.3
Flanagan, C.A.4
Morgan, K.5
Maudsley, S.R.6
-
2
-
-
0026020369
-
Clinical uses of gonadotropin-releasing hormone analogs
-
Casper, R. F. (1991) Clinical uses of gonadotropin-releasing hormone analogs. Can. Med. Assoc. J. 144, 153-158.
-
(1991)
Can. Med. Assoc. J
, vol.144
, pp. 153-158
-
-
Casper, R.F.1
-
3
-
-
0028306250
-
Gonadotropin-releasing hormone and its analogs
-
Conn, P. M., and Crowley, W. F., Jr. (1994) Gonadotropin-releasing hormone and its analogs. Annu. Rev. Med. 45, 391-405.
-
(1994)
Annu. Rev. Med
, vol.45
, pp. 391-405
-
-
Conn, P.M.1
Crowley Jr., W.F.2
-
4
-
-
37549054715
-
Diversity of actions of GnRHs mediated by ligand-induced selective signaling
-
Millar, R. P., Pawson, A. J., Morgan, K., Rissman, E. F., and Lu, Z. L. (2008) Diversity of actions of GnRHs mediated by ligand-induced selective signaling. Front. Neuroendocrinol. 29, 17-35.
-
(2008)
Front. Neuroendocrinol
, vol.29
, pp. 17-35
-
-
Millar, R.P.1
Pawson, A.J.2
Morgan, K.3
Rissman, E.F.4
Lu, Z.L.5
-
5
-
-
23844481788
-
Mutations remote from the human gonadotropin-releasing hormone (GnRH) receptor binding sites specifically increase binding affinity for GnRH II, but not GnRH I: Evidence for ligand-selective receptor active conformations
-
Lu, Z. L., Gallagher, R., Sellar, R., Coetsee, M., and Millar, R. P. (2005) Mutations remote from the human gonadotropin-releasing hormone (GnRH) receptor binding sites specifically increase binding affinity for GnRH II, but not GnRH I: Evidence for ligand-selective receptor active conformations. J. Biol. Chem. 280, 29796-29803.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 29796-29803
-
-
Lu, Z.L.1
Gallagher, R.2
Sellar, R.3
Coetsee, M.4
Millar, R.P.5
-
6
-
-
43949095157
-
On the applicability of GPCR homology models to computer-aided drug discovery: A comparison between in silico and crystal structures of the beta2-adrenergic receptor
-
Costanzi, S. (2008) On the applicability of GPCR homology models to computer-aided drug discovery: A comparison between in silico and crystal structures of the beta2-adrenergic receptor. J. Med. Chem. 51, 2907-2914.
-
(2008)
J. Med. Chem
, vol.51
, pp. 2907-2914
-
-
Costanzi, S.1
-
7
-
-
0034948696
-
Structural mimicry in G protein-coupled receptors: Implications of the high-resolution structure of rhodopsin for structure-function analysis of rhodopsin-like receptors
-
Ballesteros, J. A., Shi, L., and Javitch, J. A. (2001) Structural mimicry in G protein-coupled receptors: Implications of the high-resolution structure of rhodopsin for structure-function analysis of rhodopsin-like receptors. Mol. Pharmacol. 60, 1-19.
-
(2001)
Mol. Pharmacol
, vol.60
, pp. 1-19
-
-
Ballesteros, J.A.1
Shi, L.2
Javitch, J.A.3
-
8
-
-
0036499727
-
Seven-transmembrane receptors: Crystals clarify
-
Lu, Z. L., Saldanha, J. W., and Hulme, E. C. (2002) Seven-transmembrane receptors: Crystals clarify. Trends Pharmacol. Sci. 23, 140-146.
-
(2002)
Trends Pharmacol. Sci
, vol.23
, pp. 140-146
-
-
Lu, Z.L.1
Saldanha, J.W.2
Hulme, E.C.3
-
9
-
-
0036169280
-
The binding site of aminergic G protein-coupled receptors: The transmembrane segments and second extracellular loop
-
Shi, L., and Javitch, J. A. (2002) The binding site of aminergic G protein-coupled receptors: the transmembrane segments and second extracellular loop. Annu. Rev. Pharmacol. Toxicol. 42, 437-467.
-
(2002)
Annu. Rev. Pharmacol. Toxicol
, vol.42
, pp. 437-467
-
-
Shi, L.1
Javitch, J.A.2
-
10
-
-
33144459843
-
Molecular mechanism of 7TM receptor activation-a global toggle switch model
-
Schwartz, T. W., Frimurer, T. M., Holst, B., Rosenkilde, M. M., and Elling, C. E. (2006) Molecular mechanism of 7TM receptor activation-a global toggle switch model. Annu. Rev. Pharmacol. Toxicol. 46, 481-519.
-
(2006)
Annu. Rev. Pharmacol. Toxicol
, vol.46
, pp. 481-519
-
-
Schwartz, T.W.1
Frimurer, T.M.2
Holst, B.3
Rosenkilde, M.M.4
Elling, C.E.5
-
11
-
-
36448978229
-
2-adrenergic receptor function
-
2-adrenergic receptor function. Science 318, 1266-1273.
-
(2007)
Science
, vol.318
, pp. 1266-1273
-
-
Rosenbaum, D.M.1
Cherezov, V.2
Hanson, M.A.3
Rasmussen, S.G.F.4
Thian, F.S.5
Kobilka, T.S.6
Choi, H.J.7
Yao, X.J.8
Weis, W.I.9
Stevens, R.C.10
Kobilka, B.K.11
-
12
-
-
40149095112
-
3 muscarinic acetylcholine receptor structure detected by a disulfide scaning strategy
-
3 muscarinic acetylcholine receptor structure detected by a disulfide scaning strategy. Biochemistry 47, 2776-2788.
-
(2008)
Biochemistry
, vol.47
, pp. 2776-2788
-
-
Li, J.H.1
Hamdan, F.F.2
Kim, S.-K.3
Jacobson, K.A.4
Zhang, X.5
Han, S.-J.6
Wess, J.7
-
13
-
-
0037192126
-
Impact of aromatic residues within transmembrane helix 6 of the human gonadotropin-releasing hormone receptor upon agonist and antagonist binding
-
Hovelmann, S., Hoffmann, S. H., Kuhne, R., ter Laak, T., Reilander, H., and Beckers, T. (2002) Impact of aromatic residues within transmembrane helix 6 of the human gonadotropin-releasing hormone receptor upon agonist and antagonist binding. Biochemistry 41, 1129-1136.
-
(2002)
Biochemistry
, vol.41
, pp. 1129-1136
-
-
Hovelmann, S.1
Hoffmann, S.H.2
Kuhne, R.3
ter Laak, T.4
Reilander, H.5
Beckers, T.6
-
15
-
-
0027986888
-
The ligand binding site of the neurokinin 2 receptor: Site-directed mutagenesis and identification of neurokinin A binding residues in the human neurokinin 2 receptor
-
Bhogal, N., Donnelly, D., and Findlay, J. B. (1994) The ligand binding site of the neurokinin 2 receptor: Site-directed mutagenesis and identification of neurokinin A binding residues in the human neurokinin 2 receptor. J. Biol. Chem. 269, 27269-27274.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 27269-27274
-
-
Bhogal, N.1
Donnelly, D.2
Findlay, J.B.3
-
16
-
-
0029025788
-
Mutagenesis and the molecular modeling of the rat angiotensin II receptor (AT1)
-
Yamano, Y., Ohyama, K., Kikyo, M., Sano, T., Nakagomi, Y., Inoue, Y., Nakamura, N., Morishima, I., Guo, D. F., and Hamakubo, T. (1995) Mutagenesis and the molecular modeling of the rat angiotensin II receptor (AT1). J. Biol. Chem. 270, 14024-14030.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 14024-14030
-
-
Yamano, Y.1
Ohyama, K.2
Kikyo, M.3
Sano, T.4
Nakagomi, Y.5
Inoue, Y.6
Nakamura, N.7
Morishima, I.8
Guo, D.F.9
Hamakubo, T.10
-
17
-
-
0027933626
-
Complete mutagenesis of the extracellular domain of interleukin-8 (IL- 8) type A receptor identifies charged residues mediating IL-8 binding and signal transduction
-
Leong, S. R., Kabakoff, R. C., and Hebert, C. A. (1994) Complete mutagenesis of the extracellular domain of interleukin-8 (IL- 8) type A receptor identifies charged residues mediating IL-8 binding and signal transduction. J. Biol. Chem. 269, 19343-19348.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 19343-19348
-
-
Leong, S.R.1
Kabakoff, R.C.2
Hebert, C.A.3
-
18
-
-
0343550426
-
Functional importance of transmembrane helix 6 Trp(279) and exoloop 3 Val(299) of rat gonadotropin-releasing hormone receptor
-
Chauvin, S., Berault, A., Lerrant, Y., Hibert, M., and Counis, R. (2000) Functional importance of transmembrane helix 6 Trp(279) and exoloop 3 Val(299) of rat gonadotropin-releasing hormone receptor. Mol. Pharmacol. 57, 625-633.
-
(2000)
Mol. Pharmacol
, vol.57
, pp. 625-633
-
-
Chauvin, S.1
Berault, A.2
Lerrant, Y.3
Hibert, M.4
Counis, R.5
-
19
-
-
34547096510
-
Structural determinants for ligand-receptor conformational selection in a peptide G protein-coupled receptor
-
Lu, Z. L., Coetsee, M., White, C. D., and Millar, R. P. (2007) Structural determinants for ligand-receptor conformational selection in a peptide G protein-coupled receptor. J. Biol. Chem. 282, 17921-17929.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 17921-17929
-
-
Lu, Z.L.1
Coetsee, M.2
White, C.D.3
Millar, R.P.4
-
20
-
-
52949127931
-
Role of Trp280(6.48) in the gonadotrophin-releasing hormone (GnRH) receptor
-
Glasgow, U.K, July 23-27, Abstract 0518, The Biochemical Society, London, U.K
-
Coetsee, M., Gallagher, R., Millar, R. P., Flanagan, C. A., and Lu, Z. L. (2006) Role of Trp280(6.48) in the gonadotrophin-releasing hormone (GnRH) receptor. BioScience 2006, Glasgow, U.K., July 23-27, 2006, Abstract 0518, The Biochemical Society, London, U.K.
-
(2006)
BioScience 2006
-
-
Coetsee, M.1
Gallagher, R.2
Millar, R.P.3
Flanagan, C.A.4
Lu, Z.L.5
-
21
-
-
0034682639
-
2.61(98) side chain of the gonadotropin-releasing hormone receptor contribute differentially to ligand interaction
-
2.61(98) side chain of the gonadotropin-releasing hormone receptor contribute differentially to ligand interaction. Biochemistry 39, 8133-8141.
-
(2000)
Biochemistry
, vol.39
, pp. 8133-8141
-
-
Flanagan, C.A.1
Rodic, V.2
Konvicka, K.3
Yuen, T.4
Chi, L.5
Rivier, J.E.6
Millar, R.P.7
Weinstein, H.8
Sealfon, S.C.9
-
22
-
-
0031037632
-
1 muscarinic receptor: Mutations of aspartate 122 and tyrosine 124 decrease receptor expression but do not abolish signaling
-
1 muscarinic receptor: mutations of aspartate 122 and tyrosine 124 decrease receptor expression but do not abolish signaling. Mol. Pharmacol. 51, 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
-
-
33750836895
-
Crystal structure of a photoactivated deprotonated intermediate of rhodopsin
-
Salom, D., Lodowski, D. T., Stenkamp, R. E., Le Trong, I., Golczak, M., Jastrzebska, B., Harris, T., Ballesteros, J. A., and Palczewski, K. (2006) Crystal structure of a photoactivated deprotonated intermediate of rhodopsin. Proc. Natl. Acad. Sci. U.S.A. 103, 16123-16128.
-
(2006)
Proc. Natl. Acad. Sci. U.S.A
, vol.103
, pp. 16123-16128
-
-
Salom, D.1
Lodowski, D.T.2
Stenkamp, R.E.3
Le Trong, I.4
Golczak, M.5
Jastrzebska, B.6
Harris, T.7
Ballesteros, J.A.8
Palczewski, K.9
-
24
-
-
33845988716
-
Conserved amino acid residues that are important for ligand binding in the type I gonadotropin-releasing hormone (GnRH) receptor are required for high potency of GnRH II at the type II GnRH receptor
-
Mamputha, S., Lu, Z. L., Roeske, R. W., Millar, R. P., Katz, A. A., and Flanagan, C. A. (2007) Conserved amino acid residues that are important for ligand binding in the type I gonadotropin-releasing hormone (GnRH) receptor are required for high potency of GnRH II at the type II GnRH receptor. Mol. Endocrinol. 21, 281-292.
-
(2007)
Mol. Endocrinol
, vol.21
, pp. 281-292
-
-
Mamputha, S.1
Lu, Z.L.2
Roeske, R.W.3
Millar, R.P.4
Katz, A.A.5
Flanagan, C.A.6
-
25
-
-
0034464661
-
Residues within transmembrane helices 2 and 5 of the human gonadotropin-releasing hormone receptor contribute to agonist and antagonist binding
-
Hoffmann, S. H., ter Laak, T. T., Kuhne, R., Reilander, H., and Beckers, T. (2000) Residues within transmembrane helices 2 and 5 of the human gonadotropin-releasing hormone receptor contribute to agonist and antagonist binding. Mol. Endocrinol. 14, 1099-1115.
-
(2000)
Mol. Endocrinol
, vol.14
, pp. 1099-1115
-
-
Hoffmann, S.H.1
ter Laak, T.T.2
Kuhne, R.3
Reilander, H.4
Beckers, T.5
-
26
-
-
0029666304
-
Asn102 of the gonadotropin-releasing hormone receptor is a critical determinant of potency for agonists containing C-terminal glycinamide
-
Davidson, J. S., McArdle, C. A., Davies, P. D., Elario, R., Flanagan, C. A., and Millar, R. P. (1996) Asn102 of the gonadotropin-releasing hormone receptor is a critical determinant of potency for agonists containing C-terminal glycinamide. J. Biol. Chem. 271, 15510-15514.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 15510-15514
-
-
Davidson, J.S.1
McArdle, C.A.2
Davies, P.D.3
Elario, R.4
Flanagan, C.A.5
Millar, R.P.6
-
27
-
-
84986512474
-
CHARMM: A program for macromolecular energy minimization and dynamics calculations
-
Brooks, B. R., Bruccoleri, R. E., Olason, B. D., States, D. J., Swaminathan, S., and Karplus, M. (1983) CHARMM: A program for macromolecular energy minimization and dynamics calculations. J. Comput. Chem. 4, 187-217.
-
(1983)
J. Comput. Chem
, vol.4
, pp. 187-217
-
-
Brooks, B.R.1
Bruccoleri, R.E.2
Olason, B.D.3
States, D.J.4
Swaminathan, S.5
Karplus, M.6
-
28
-
-
23044445866
-
The DRY motif as a molecular switch of the human oxytocin receptor
-
Favre, N., Fanelli, F., Missotten, M., Nichols, A., Wilson, J., di Tiani, M., Rommel, C., and Scheer, A. (2005) The DRY motif as a molecular switch of the human oxytocin receptor. Biochemistry 44, 9990-10008.
-
(2005)
Biochemistry
, vol.44
, pp. 9990-10008
-
-
Favre, N.1
Fanelli, F.2
Missotten, M.3
Nichols, A.4
Wilson, J.5
di Tiani, M.6
Rommel, C.7
Scheer, A.8
-
29
-
-
0036643478
-
The nature of intermolecular interactions between aromatic amino acid residues. Proteins: Struct., Funct
-
Gervasio, F. L., Chelli, R., Procacci, P., and Schettino, V. (2002) The nature of intermolecular interactions between aromatic amino acid residues. Proteins: Struct., Funct., Bioinformatics 48, 117-125.
-
(2002)
Bioinformatics
, vol.48
, pp. 117-125
-
-
Gervasio, F.L.1
Chelli, R.2
Procacci, P.3
Schettino, V.4
-
30
-
-
0021828928
-
Hydrogen bonding and biological specificity analysed by protein engineering
-
Fersht, A. R., Shi, J. P., Knill-Jones, J., Lowe, D. M., Wilkinson, A. J., Blow, D. M., Brick, P., Carter, P., Waye, M. M., and Winter, G. (1985) Hydrogen bonding and biological specificity analysed by protein engineering. Nature 314, 235-238.
-
(1985)
Nature
, vol.314
, pp. 235-238
-
-
Fersht, A.R.1
Shi, J.P.2
Knill-Jones, J.3
Lowe, D.M.4
Wilkinson, A.J.5
Blow, D.M.6
Brick, P.7
Carter, P.8
Waye, M.M.9
Winter, G.10
-
31
-
-
1042263794
-
Aromatic side-chain interactions in proteins: Near- and far-sequence Tyr-X pairs
-
Meurisse, R., Brasseur, R., and Thomas, A. (2004) Aromatic side-chain interactions in proteins: Near- and far-sequence Tyr-X pairs. Proteins: Structure, Function, and Bioinf. 54, 478-490.
-
(2004)
Proteins: Structure, Function, and Bioinf. 54
, pp. 478-490
-
-
Meurisse, R.1
Brasseur, R.2
Thomas, A.3
-
32
-
-
0032546782
-
π-stacking interactions:Alive and well in proteins
-
McGaughey, G. B., Gagne, M., and Rappe, A. K. (1998) π-stacking interactions:Alive and well in proteins. J. Biol. Chem. 273, 15458-15463.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 15458-15463
-
-
McGaughey, G.B.1
Gagne, M.2
Rappe, A.K.3
-
33
-
-
0029135443
-
A locus of the gonadotropin-releasing hormone receptor which differentiates agonist and antagonist binding sites
-
Zhou, W., Rodic, V., Kitanovic, S., Flanagan, C. A., Chi, L., Weinstein, H., Maayani, S., Millar, R. P., and Sealfon, S. C. (1995) A locus of the gonadotropin-releasing hormone receptor which differentiates agonist and antagonist binding sites. J. Biol. Chem. 270, 18853-18857.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 18853-18857
-
-
Zhou, W.1
Rodic, V.2
Kitanovic, S.3
Flanagan, C.A.4
Chi, L.5
Weinstein, H.6
Maayani, S.7
Millar, R.P.8
Sealfon, S.C.9
-
34
-
-
0034747357
-
Role of aspartate7.32(302) of the human gonadotropin-releasing hormone receptor in stabilizing a high-affinity ligand conformation
-
Fromme, B. J., Katz, A. A., Roeske, R. W., Millar, R. P., and Flanagan, C. A. (2001) Role of aspartate7.32(302) of the human gonadotropin-releasing hormone receptor in stabilizing a high-affinity ligand conformation. Mol. Pharmacol. 60, 1280-1287.
-
(2001)
Mol. Pharmacol
, vol.60
, pp. 1280-1287
-
-
Fromme, B.J.1
Katz, A.A.2
Roeske, R.W.3
Millar, R.P.4
Flanagan, C.A.5
-
35
-
-
27644450114
-
The N-terminal juxtamembrane segment of the V1a vasopressin receptor provides two independent epitopes required for high-affinity agonist binding and signaling
-
Hawtin, S. R., Wesley, V. J., Simms, J., Argent, C. C., Latif, K., and Wheatley, M. (2005) The N-terminal juxtamembrane segment of the V1a vasopressin receptor provides two independent epitopes required for high-affinity agonist binding and signaling. Mol. Endocrinol. 19, 2871-2881.
-
(2005)
Mol. Endocrinol
, vol.19
, pp. 2871-2881
-
-
Hawtin, S.R.1
Wesley, V.J.2
Simms, J.3
Argent, C.C.4
Latif, K.5
Wheatley, M.6
-
36
-
-
0030937284
-
Molecular mechanisms of ligand interaction with the gonadotropin-releasing hormone receptor
-
Sealfon, S. C., Weinstein, H., and Millar, R. P. (1997) Molecular mechanisms of ligand interaction with the gonadotropin-releasing hormone receptor. Endocr. Rev. 18, 180-205.
-
(1997)
Endocr. Rev
, vol.18
, pp. 180-205
-
-
Sealfon, S.C.1
Weinstein, H.2
Millar, R.P.3
-
37
-
-
0028100755
-
Glutamate 301 of the mouse gonadotropin-releasing hormone receptor confers specificity for Arginine 8 of mammalian gonadotropin-releasing hormone
-
Flanagan, C. A., Becker, I. I., Davidson, J. S., Wakefield, I. K., Zhou, W., Sealfon, S. C., and Millar, R. P. (1994) Glutamate 301 of the mouse gonadotropin-releasing hormone receptor confers specificity for Arginine 8 of mammalian gonadotropin-releasing hormone. J. Biol. Chem. 269, 22636-22641.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 22636-22641
-
-
Flanagan, C.A.1
Becker, I.I.2
Davidson, J.S.3
Wakefield, I.K.4
Zhou, W.5
Sealfon, S.C.6
Millar, R.P.7
-
38
-
-
31544438603
-
Overlapping, nonidentical binding sites of different classes of nonpeptide antagonists for the human gonadotropin-releasing hormone receptor
-
Betz, S. F., Reinhart, G. J., Lio, F. M., Chen, C., and Struthers, R. S. (2006) Overlapping, nonidentical binding sites of different classes of nonpeptide antagonists for the human gonadotropin-releasing hormone receptor. J. Med. Chem. 49, 637-647.
-
(2006)
J. Med. Chem
, vol.49
, pp. 637-647
-
-
Betz, S.F.1
Reinhart, G.J.2
Lio, F.M.3
Chen, C.4
Struthers, R.S.5
-
40
-
-
0030671469
-
Agonist-specific receptor conformations
-
Kenakin, T. (1997) Agonist-specific receptor conformations. Trends Pharmacol. Sci. 18, 416-417.
-
(1997)
Trends Pharmacol. Sci
, vol.18
, pp. 416-417
-
-
Kenakin, T.1
|