메뉴 건너뛰기




Volumn 53, Issue 3, 1998, Pages 370-376

Chloroethylclonidine binds irreversibly to exposed cysteines in the fifth membrane-spanning domain of the human α2(A)-adrenergic receptor

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 2A ADRENERGIC RECEPTOR; CHLOROETHYLCLONIDINE; CLONIDINE; RECEPTOR SUBTYPE;

EID: 0345259510     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.53.3.370     Document Type: Article
Times cited : (32)

References (33)
  • 1
    • 0027506471 scopus 로고
    • The probable arrangement of the helices in G protein-coupled receptors
    • Baldwin JM (1993) The probable arrangement of the helices in G protein-coupled receptors. EMBO J 12:1693-1703.
    • (1993) EMBO J , vol.12 , pp. 1693-1703
    • Baldwin, J.M.1
  • 2
    • 0030040907 scopus 로고    scopus 로고
    • The conserved aspartate residue in the third putative transmembrane domain of the delta-opioid receptor is not the anionic counterpart for cationic opiate binding but is a constituent of the receptor binding site
    • Befort K, Tabbara L, Bausch S, Chavkin C, Evans C, and Keiffer B (1996) The conserved aspartate residue in the third putative transmembrane domain of the delta-opioid receptor is not the anionic counterpart for cationic opiate binding but is a constituent of the receptor binding site. Mol Pharmacol 49:216-223.
    • (1996) Mol Pharmacol , vol.49 , pp. 216-223
    • Befort, K.1    Tabbara, L.2    Bausch, S.3    Chavkin, C.4    Evans, C.5    Keiffer, B.6
  • 6
    • 0027092318 scopus 로고
    • Molecular basis for species selectivity of the neurokinin-1 receptor antagonists CP-96,345 and RP67580
    • Fong TM, Yu H, and Strader CD (1992) Molecular basis for species selectivity of the neurokinin-1 receptor antagonists CP-96,345 and RP67580. J Biol Chem 267: 25668-25671.
    • (1992) J Biol Chem , vol.267 , pp. 25668-25671
    • Fong, T.M.1    Yu, H.2    Strader, C.D.3
  • 7
    • 0029757635 scopus 로고    scopus 로고
    • Residues in the seventh membrane-spanning segment of the dopamine D2 receptor accessible in the binding-site crevice
    • Fu D, Ballesteros JA, Weinstein H, Chen J, and Javitch JA (1996) Residues in the seventh membrane-spanning segment of the dopamine D2 receptor accessible in the binding-site crevice. Biochemistry 35:11278-11285.
    • (1996) Biochemistry , vol.35 , pp. 11278-11285
    • Fu, D.1    Ballesteros, J.A.2    Weinstein, H.3    Chen, J.4    Javitch, J.A.5
  • 10
    • 0023513551 scopus 로고
    • 1-adrenergic receptors revealed by chlorethylclonidine
    • 1-adrenergic receptors revealed by chlorethylclonidine. Mol Pharmacol 32:505-510.
    • (1987) Mol Pharmacol , vol.32 , pp. 505-510
    • Han, C.1    Abel, P.W.2    Minneman, K.P.3
  • 11
    • 0025292355 scopus 로고
    • Model for structure of bacteriorhodopsin based on high-resolution electron cryomicroscopy
    • Henderson R, Baldwin JM, Ceska TA, Zemlin F, Backmann E, and Downing KH (1990) Model for structure of bacteriorhodopsin based on high-resolution electron cryomicroscopy. J Mol Biol 213:899-929.
    • (1990) J Mol Biol , vol.213 , pp. 899-929
    • Henderson, R.1    Baldwin, J.M.2    Ceska, T.A.3    Zemlin, F.4    Backmann, E.5    Downing, K.H.6
  • 12
    • 0029117219 scopus 로고
    • 1-adrenergic receptor subtype selective agonist binding
    • 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
  • 14
    • 0029617613 scopus 로고
    • Residues in the fifth membrane-spanning segment of the dopamine D2 receptor exposed in the binding-site crevice
    • Javitch JA, Fu D, and Chen J (1995) Residues in the fifth membrane-spanning segment of the dopamine D2 receptor exposed in the binding-site crevice. Biochemistry 34:16433-16439.
    • (1995) Biochemistry , vol.34 , pp. 16433-16439
    • Javitch, J.A.1    Fu, D.2    Chen, J.3
  • 20
    • 0022005744 scopus 로고
    • Analysis of radioligand binding experiments: A collection of computer programs for the IBM PC
    • McPherson GA (1985) Analysis of radioligand binding experiments: a collection of computer programs for the IBM PC. J Pharmacol Methods 14:213-229.
    • (1985) J Pharmacol Methods , vol.14 , pp. 213-229
    • McPherson, G.A.1
  • 22
  • 24
    • 0027533429 scopus 로고
    • Molecular basis for the species selectivity of the substance P antagonist CP-96345
    • Sachais B, Snider R, Lowe J, and Krause J (1993) Molecular basis for the species selectivity of the substance P antagonist CP-96345. J Biol Chem 268:2319-2323.
    • (1993) J Biol Chem , vol.268 , pp. 2319-2323
    • Sachais, B.1    Snider, R.2    Lowe, J.3    Krause, J.4
  • 25
    • 0026548156 scopus 로고
    • In vitro mutagenesis and the search for structure-function relationships among G protein coupled receptors
    • Savarese TM and Fraser CM (1992) In vitro mutagenesis and the search for structure-function relationships among G protein coupled receptors. Biochem J 283:1-19.
    • (1992) Biochem J , vol.283 , pp. 1-19
    • Savarese, T.M.1    Fraser, C.M.2
  • 27
    • 0027933763 scopus 로고
    • Locating ligand-binding sites in 7TM receptors by protein engineering
    • Schwartz TW (1994) Locating ligand-binding sites in 7TM receptors by protein engineering. Curr Opin Biotechnol 5:434-444.
    • (1994) Curr Opin Biotechnol , vol.5 , pp. 434-444
    • Schwartz, T.W.1
  • 28
    • 0024344941 scopus 로고
    • Identification of two serine residues involved in agonist activation of the β-adrenergic receptor
    • Strader CD, Candelore MR, Hill WS, Sigal IS, and Dixon RAF (1989) Identification of two serine residues involved in agonist activation of the β-adrenergic receptor. J Biol Chem 264:13572-1357.
    • (1989) J Biol Chem , vol.264 , pp. 13572-21357
    • Strader, C.D.1    Candelore, M.R.2    Hill, W.S.3    Sigal, I.S.4    Dixon, R.A.F.5
  • 30
    • 0025367825 scopus 로고
    • Species differences in chlorethylclonidine antagonism at vascular alpha1 adrenergic receptors
    • Tian WN, Gupta S, and Deth RC (1990) Species differences in chlorethylclonidine antagonism at vascular alpha1 adrenergic receptors. J Pharmacol Exp Ther 253: 877-883.
    • (1990) J Pharmacol Exp Ther , vol.253 , pp. 877-883
    • Tian, W.N.1    Gupta, S.2    Deth, R.C.3
  • 31
    • 0027451513 scopus 로고
    • Cardiovascular effects of chloroethylclonidine, an irreversible α1B adrenoceptor antagonist, in the unanesthetized rat: A pharmacological analysis in vivo and in vitro
    • Vargas HM, Cunningham D, Zhou L, Hartman HB, and Gorman AJ (1993) Cardiovascular effects of chloroethylclonidine, an irreversible α1B adrenoceptor antagonist, in the unanesthetized rat: a pharmacological analysis in vivo and in vitro. J Pharmacol Exp Ther 266:864-871.
    • (1993) J Pharmacol Exp Ther , vol.266 , pp. 864-871
    • Vargas, H.M.1    Cunningham, D.2    Zhou, L.3    Hartman, H.B.4    Gorman, A.J.5
  • 32
    • 0026006986 scopus 로고
    • 2A-adrenergic receptors: Identification of amino acids involved in ligand binding and receptor activation by agonists
    • 2A-adrenergic receptors: identification of amino acids involved in ligand binding and receptor activation by agonists. Mol Pharmacol 40:168-179.
    • (1991) Mol Pharmacol , vol.40 , pp. 168-179
    • Wang, C.-D.1    Buck, M.A.2    Fraser, C.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.